The DISabled to ENabled podcast for people with chronic illnesses: Recent Episodes
Jessie Ace
DISabled to ENabled podcast is the podcast for people with chronic illnesses. Join British host Jessie Ace as she interviews inspiring people affected by chronic illness who turned their diagnosis into something unexpected. Listen to people such as celebrities/CEOs/athletes/marathon runners as well as real-life stories as they let you into their lives and how they did something awesome despite their chronic illness diagnosis. Learn their tips, tricks, and advice for living your best life with your chronic illness. We discuss hard topics with a side of positivity and humor as we navigate life.
In this episode, you’ll learn Katie's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Katie's links:IG: @katiecolletttvwavy.com Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace's illustrations on www.Jessieace.com
In this episode, you’ll learn more about MS Advocacy on local TV news as we carry on our chat with Katie Collett. Tune in to the last part of our interview where we find out about Katie's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Katie's links:IG: @katiecolletttvwavy.com Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com
In this episode, you’ll learn more about Multiple Sclerosis as we chat with Katie Collett about her diagnosis. The highs and the lows. Symptoms to medication to things she’s found to help her condition. In the next episode find out about how she has raised awareness for MS alongside her day job as a TV news anchor! Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Katie's links:IG: @katiecolletttvwavy.com Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com
In this episode, you’ll learn Damian's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Want to WIN a copy of our best selling ENabled Warrior Symptom Tracker? Enter the giveaway by going to www.mybookgiveaway.com to enter your details in Facebook messenger (lookout for a link that will pop up!) Or if you’re impatient (like me) and want yours now, Claim your discounted book from www.enabledwarriors.org/book Check out Damian’s links:www.DamianWashington.comInstagram: DamianWashingtonFacebook: facebook.com/DamianWashington03 Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com
In this episode, you’ll learn more about Multiple Sclerosis as we carry on our chat with Damian Washington. Tune in to the last part of our interview where we find out about Damian's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Damian’s links:www.DamianWashington.comInstagram: DamianWashingtonFacebook: facebook.com/DamianWashington03 Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey as an illustrator on www.jessieace.com
In this episode, you’ll learn more about Multiple Sclerosis as we chat with Damian Washington about his diagnosis. The highs and the lows. Symptoms to medication to things she’s found to help his condition. In the next episode find out about his line of work and his YouTube channel, NoStressMS. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Damian’s links:www.DamianWashington.comInstagram: DamianWashingtonFacebook: facebook.com/DamianWashington03 Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled
In our MS nurse special, we chat with MS specialist nurse Fiona Cray (who's actually my very own MS nurse). In the final part of our MS nurse special, Fiona answers your questions about MS from the ENabled Warriors Facebook group. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Newly diagnosed? Check out these links:MS TrustMS-UKNational MS SocietyMS SocietyMS Focus Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled
In our MS nurse special, we chat with MS specialist nurse Fiona Cray (who's actually my very own MS nurse). In part 4 we're chatting about DMTs and symptoms. Listen out for the final episode as we ask Fiona your questions about MS from the ENabled Warriors group. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Newly diagnosed? Check out these links:MS TrustMS-UKNational MS SocietyMS SocietyMS Focus Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled
In our MS nurse special, we chat with MS specialist nurse Fiona Cray (who's actually my very own MS nurse). In part 3 let's dispel the myths around MS Listen out for the next episodes where we discuss DMTs, symptoms, and your questions from the ENabled Warriors group. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Newly diagnosed? Check out these links:MS TrustMS-UKNational MS SocietyMS SocietyMS Focus Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled
In our MS nurse special, we chat with MS specialist nurse Fiona Cray (who's actually my very own MS nurse). In part 2 learn about what MS actually is and how it really affects our bodies. Listen out for the next episodes talking about DMTs, symptoms, myths and your questions from the ENabled Warriors group in part 5! Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker.Newly diagnosed? Check out these links:MS TrustMS-UKNational MS SocietyMS SocietyMS Focus Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled
In our MS nurse special, we chat with MS specialist nurse Fiona Cray (who's actually my very own MS nurse). In part 1 we describe who Fiona is. Listen out for her next episodes where we discuss what MS actually is, myths surrounding MS, DMTs, and symptoms. Listen out for your questions from the ENabled Warriors group in part 5! Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Newly diagnosed? Check out these links:MS TrustMS-UKNational MS SocietyMS SocietyMS Focus Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled
In this episode, you’ll learn Marissa's not-so-super-quick secrets. You’ll discover her favourite book, favourite place, scariest thing she's done and (our favourite) the weirdest thing she's ever done too. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Connect with Marissa:Instagram - @mcgreen2 LinkedIn - https://www.linkedin.com/in/marissa-charlotte-green-4150219b/ Twitter - @marissachgreen Connect with the MS Trust:Website: https://www.mstrust.org.uk/Instagram: https://www.instagram.com/ms_trust/Twitter: https://twitter.com/MSTrustFacebook: https://www.facebook.com/mstrustuk Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled
In this episode, you’ll learn more about her charity challenges as we carry on our chat with Marissa Green.Tune in to the last part of our interview where we find out about Marissa's not-so-super-quick secrets. You’ll discover her favourite book, favourite place, scariest thing she's done and (our favourite) the weirdest thing she's ever done too. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Connect with Marissa:Instagram - @mcgreen2 LinkedIn - https://www.linkedin.com/in/marissa-charlotte-green-4150219b/ Twitter - @marissachgreen Connect with the MS Trust:Website: https://www.mstrust.org.uk/Instagram: https://www.instagram.com/ms_trust/Twitter: https://twitter.com/MSTrustFacebook: https://www.facebook.com/mstrustuk Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled
In this episode, you’ll learn more about Balo's Concentric Sclerosis and Relapsing-Remitting Multiple Sclerosis as we chat with Marissa Green about her diagnoses. The highs and the lows. Symptoms to medication to things she’s found to help her condition. In part 2 find out about all the amazing work she does with The MS Trust. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Connect with Marissa:Instagram - @mcgreen2 LinkedIn - https://www.linkedin.com/in/marissa-charlotte-green-4150219b/ Twitter - @marissachgreen Connect with the MS Trust:Website: https://www.mstrust.org.uk/Instagram: https://www.instagram.com/ms_trust/Twitter: https://twitter.com/MSTrustFacebook: https://www.facebook.com/mstrustuk Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled
In this episode, you’ll learn Daana and Dawn's not-so-super-quick secrets. You’ll discover their favourite books, favourite places, scariest things they’ve done and (our favourite) the weirdest things they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out the Girls' links:Myelinandmelanin@gmail.comIG/FB/Twitter @myelinmelaninYoutube: Myelinmelanin@youtube.com Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com
In this episode, you’ll learn more about how the Myelin and Melanin podcast began as we carry on our chat with Daan and Dawn. Tune in to the last part of our interview where we find out about Daana and Dawn's not-so-super-quick secrets. You’ll discover their favourite books, favourite places, scariest things they’ve done and (our favourite) the weirdest things they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out the Girls' links:Myelinandmelanin@gmail.comIG/FB/Twitter @myelinmelaninYoutube: Myelinmelanin@youtube.com Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com
In this episode, you’ll learn more about Multiple Sclerosis as we chat with Daana & Dawn about their diagnoses. The highs and the lows. Symptoms to medication to things they've found to help their conditions. In the next episode find out about how they began the Myelin and Melanin podcast together. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out the Girls' links:Myelinandmelanin@gmail.comIG/FB/Twitter @myelinmelaninYoutube: Myelinmelanin@youtube.com Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com
In this episode, you’ll learn Nikky's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Nikky's links:www.innabox.co.ukWww.instagram.com/innaboxdesignWww.facebook.com/innaboxdesignWww.twitter.com/innaboxdesign Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com
In this episode, you’ll learn more about how Innabox Designs was born as we carry on our chat with Nikky. Tune in to the last part of our interview where we find out about Nikky's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Nikky's links:www.innabox.co.ukWww.instagram.com/innaboxdesignWww.facebook.com/innaboxdesignWww.twitter.com/innaboxdesign Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com
In this episode, you’ll learn more about Endometriosis as we chat with Nikky about her diagnosis. The highs and the lows. Symptoms to medication to things she’s found to help her condition. In the next episode find out about how she turned things on their head and began Innabox Designs. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Nikky's links:www.innabox.co.ukWww.instagram.com/innaboxdesignWww.facebook.com/innaboxdesignWww.twitter.com/innaboxdesign Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com
In this episode, you’ll learn Dr Conor's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Guest’s links:Phytaphix.co.ukFb: https://www.facebook.com/PhytaphixIG: https://www.instagram.com/phytaphix/Twitter: https://twitter.com/phytaphixLinkedIn: https://www.linkedin.com/company/phytaphix/ Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com
Join us in this special Q+A episode with Dr. Conor Kerley as he answers questions from our ENabled Warriors Facebook Tribe (http://mmini.me/warriors) on all things diet and nutrition. Find out Dr. Conor's advice on eating nightshade vegetables, supplements to take, and what not to eat if you have Multiple Sclerosis as well as more hints and tips.Want to ask your questions to a future guest? Join our ENabled Warriors group and look out for our question posts! Click here -> http://mmini.me/warriors Where to find Dr. Kerley:Phytaphix.co.ukFb: https://www.facebook.com/PhytaphixIG: https://www.instagram.com/phytaphix/Twitter: https://twitter.com/phytaphixLinkedIn: https://www.linkedin.com/company/phytaphix/ Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker.
In this episode, you’ll learn more about how he got into the world of health and nutrition as we carry on our chat with Dr Conor. Tune in to the last part of our interview where we find out about Dr Conor's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Guest’s links:Phytaphix.co.ukFb: https://www.facebook.com/PhytaphixIG: https://www.instagram.com/phytaphix/Twitter: https://twitter.com/phytaphixLinkedIn: https://www.linkedin.com/company/phytaphix/ Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com
In this episode, you’ll learn more about Relapsing Remitting Multiple Sclerosis as we chat with Dr Conor about his diagnosis. The highs and the lows. Symptoms to medication to things he’s found to help his condition. In the next episode find out about how he went into medicine and started his company, Phytaphix. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker.Check out Guest’s links:Phytaphix.co.ukFb: https://www.facebook.com/PhytaphixIG: https://www.instagram.com/phytaphix/Twitter: https://twitter.com/phytaphixLinkedIn: https://www.linkedin.com/company/phytaphix/ Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com
In this episode, you’ll learn Dr Lee's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Guest’s links:@drleephillips- Instagram@drleephillips- Facebook@Lee59085544- Twitterwww.drleephillips.com Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com
In this episode, you’ll learn more about how he became a Certified Sex Therapist and began writing his first book as we carry on our chat with Dr Lee. Tune in to the last part of our interview where we find out about Dr Lee's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Guest’s links:@drleephillips- Instagram@drleephillips- Facebook@Lee59085544- Twitterwww.drleephillips.com Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com
In this episode, you’ll learn more about Lyme Disease as we chat with Dr. Lee Phillips about his diagnosis. The highs and the lows. Symptoms to medication to things he’s found to help his condition. In the next episode find out about how he has gone on to help lots of people with chronic illness as a sex therapist, and how he is writing a book! Want to WIN a copy of our best selling ENabled Warrior Symptom Tracker? Enter the giveaway by going to www.mybookgiveaway.com to enter your details in Facebook messenger (lookout for a link that will pop up!) Or if you’re impatient (like me) and want yours now, Claim your discounted book from www.enabledwarriors.org/book Check out Guest’s links:@drleephillips- Instagram@drleephillips- Facebook@Lee59085544- Twitterwww.drleephillips.com Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com
In this episode, you’ll learn Mathew's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Guest’s links:www.mshope.comWatch the documentary on Amazon Prime here: https://www.amazon.com/Living-Proof-Matt-Embry/dp/B07D7PF9HRClick here to start your trial of Amazon Prime to watch the free documentary: https://amzn.to/3gjjNWrFollow MS Hope on Facebook: https://www.facebook.com/teammshope/Follow MS Hope on Instagram: https://www.instagram.com/embry.mathew/Follow MS Hope on Youtube: https://www.youtube.com/channel/UCIueKQNVAung_Iekr3jlIhQDirect-MS: https://www.direct-ms.org/ Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com
In this episode, you’ll learn more about making his documentary and how he started MS Hope as we carry on our chat with Mathew Embry. Join us next time for the last part of our interview where we find out about Mathew's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Want to WIN a copy of our best selling ENabled Warrior Symptom Tracker? Enter the giveaway by going to www.mybookgiveaway.com to enter your details in Facebook messenger (lookout for a link that will pop up!) Or if you’re impatient (like me) and want yours now, Claim your discounted book from www.enabledwarriors.org/book Check out Guest’s links:www.mshope.comWatch the documentary on Amazon Prime here: https://www.amazon.com/Living-Proof-Matt-Embry/dp/B07D7PF9HRClick here to start your trial of Amazon Prime to watch the free documentary: https://amzn.to/3gjjNWrFollow MS Hope on Facebook: https://www.facebook.com/teammshope/Follow MS Hope on Instagram: https://www.instagram.com/embry.mathew/Follow MS Hope on Youtube: https://www.youtube.com/channel/UCIueKQNVAung_Iekr3jlIhQDirect-MS: https://www.direct-ms.org/ Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com
In this episode, you’ll learn more about Multiple Sclerosis as we chat with Mathew Embry about his diagnosis. The highs and the lows. Symptoms to medication to things he’s found to help his condition. In the next episode find out about how he made a documentary and started MS Hope, after following the lifestyle that his Dad researched. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Guest’s links:www.mshope.comWatch the documentary on Amazon Prime here: https://www.amazon.com/Living-Proof-Matt-Embry/dp/B07D7PF9HRClick here to start your trial of Amazon Prime to watch the free documentary: https://amzn.to/3gjjNWrFollow MS Hope on Facebook: https://www.facebook.com/teammshope/Follow MS Hope on Instagram: https://www.instagram.com/embry.mathew/Follow MS Hope on Youtube: https://www.youtube.com/channel/UCIueKQNVAung_Iekr3jlIhQDirect-MS: https://www.direct-ms.org/ Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com
In this episode, you’ll learn Ryan's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Guest’s links: https://www.cnn.com/profiles/ryan-priorRyan’s diagnosis story on CNN: https://edition.cnn.com/2018/08/08/health/iyw-ryan-me-cfs-story/index.htmlhttps://www.facebook.com/ryan.prior.144https://www.instagram.com/ryantprior/https://twitter.com/r_priorhttps://www.linkedin.com/in/ryantprior/ Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com
In this episode, you’ll learn more about how he began writing for CNN and made a social justice documentary as we carry on our chat with Ryan Prior. Tune in to the last part of our interview where we find out about Ryan's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Guest’s links: https://www.cnn.com/profiles/ryan-priorRyan’s diagnosis story on CNN: https://edition.cnn.com/2018/08/08/health/iyw-ryan-me-cfs-story/index.htmlhttps://www.facebook.com/ryan.prior.144https://www.instagram.com/ryantprior/https://twitter.com/r_priorhttps://www.linkedin.com/in/ryantprior/ Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com
In this episode, you’ll learn more about Myalgic Encephpalomyelitis (ME) /Chronic Fatigue Syndrome (CFS) as we chat with Ryan Prior about his diagnosis. The highs and the lows. Symptoms to medication to things he’s found to help his condition. In the next episode find out about how he started writing for CNN and started the Blue Ribbon Foundation. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Guest’s links: https://www.cnn.com/profiles/ryan-priorRyan’s diagnosis story on CNN: https://edition.cnn.com/2018/08/08/health/iyw-ryan-me-cfs-story/index.htmlhttps://www.facebook.com/ryan.prior.144https://www.instagram.com/ryantprior/https://twitter.com/r_priorhttps://www.linkedin.com/in/ryantprior/ Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com
In this episode, you’ll learn Caroline's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker.Check out Guest’s links:Http://girlwithms.comTwitter @thegirlwithMS Facebook.com/girlwithms.com(I’m starting a new fb for ConquerMSwithSelfCare) Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com Want to WIN $100? Just leave a review on iTunes, and at the end of each month we’ll choose one person at random to win. Here are some prompts right now to help you figure out what to put: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Unsure how to leave a review on desktop and on a Phone? Click the links to learn more. We got you covered. (Android users may need to download the apple podcasts app)
In this episode, you’ll learn more about how she built a blog and a community as we carry on our chat with Caroline Craven. Tune in to the last part of our interview where we find out about Caroline's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Guest’s links:Http://girlwithms.comTwitter @thegirlwithMS Facebook.com/girlwithms.com(I’m starting a new fb for ConquerMSwithSelfCare) Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com Want to WIN $100? Just leave a review on iTunes, and at the end of each month we’ll choose one person at random to win. Here are some prompts right now to help you figure out what to put: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Unsure how to leave a review on desktop and on a Phone? Click the links to learn more. We got you covered. (Android users may need to download the apple podcasts app)
In this episode, you’ll learn more about Multiple Sclerosis as we chat with Caroline Craven about her diagnosis. The highs and the lows. Symptoms to medication to things she’s found to help her condition. In the next episode find out about how she started blogging and building community. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Guest’s links:Http://girlwithms.comTwitter @thegirlwithMS Facebook.com/girlwithms.com(I’m starting a new fb for ConquerMSwithSelfCare) Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com Want to WIN $100? Just leave a review on iTunes, and at the end of each month we’ll choose one person at random to win. Here are some prompts right now to help you figure out what to put: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Unsure how to leave a review on desktop and on a Phone? Click the links to learn more. We got you covered. (Android users may need to download the apple podcasts app)
In this episode, you’ll learn Hannah's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Guest’s links:stickmancommunications.co.uktwitter: @stickmancripsinsta: @stickmancommsfacebook: Stickman Communications by Hannah Ensor Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com Want to WIN $100? Just leave a review on iTunes, and at the end of each month we’ll choose one person at random to win. Here are some prompts right now to help you figure out what to put: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Unsure how to leave a review on desktop and on a Phone? Click the links to learn more. We got you covered. (Android users may need to download the apple podcasts app)
In this episode, you’ll learn more about Stickman Communications and how it got started as we carry on our chat with Hannah Ensor. Tune in to the last part of our interview where we find out about Hannah's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Guest’s links:stickmancommunications.co.uktwitter: @stickmancripsinsta: @stickmancommsfacebook: Stickman Communications by Hannah Ensor Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com Want to WIN $100? Just leave a review on iTunes, and at the end of each month we’ll choose one person at random to win. Here are some prompts right now to help you figure out what to put: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Unsure how to leave a review on desktop and on a Phone? Click the links to learn more. We got you covered. (Android users may need to download the apple podcasts app)
In this episode, you’ll learn more about hypermobility and P.o.T.S. as we chat with Hannah Ensor about her diagnosis. The highs and the lows. Symptoms to medication to things she’s found to help her condition. In the next episode find out about how she developed Stickman Communications! Want to WIN a copy of our best selling ENabled Warrior Symptom Tracker? Enter the giveaway by going to www.mybookgiveaway.com to enter your details in Facebook messenger (lookout for a link that will pop up!) Or if you’re impatient (like me) and want yours now, Claim your discounted book from www.enabledwarriors.org/book Check out Guest’s links:stickmancommunications.co.uktwitter: @stickmancripsinsta: @stickmancommsfacebook: Stickman Communications by Hannah Ensor Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com Want to WIN $100? Just leave a review on iTunes, and at the end of each month we’ll choose one person at random to win. Here are some prompts right now to help you figure out what to put: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Unsure how to leave a review on desktop and on a Phone? Click the links to learn more. We got you covered. (Android users may need to download the apple podcasts app)
In this episode, you’ll learn Eva's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Guest’s links:Website https://invisiblenotbroken.com/humancare-podcastLinkedIn: https://www.linkedin.com/in/evalana/Facebook: https://www.facebook.com/elminkoff/Instagram: https://www.instagram.com/wellacopia/Youtube: https://www.youtube.com/channel/UCVOuHrKlIePZ61JBcel7dXg Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com Want to WIN $100? Just leave a review on iTunes, and at the end of each month we’ll choose one person at random to win. Here are some prompts right now to help you figure out what to put: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Unsure how to leave a review on desktop and on a Phone? Click the links to learn more. We got you covered. (Android users may need to download the apple podcasts app)
In this episode, you’ll learn more about Wellacopia and managing your symptoms naturally as we carry on our chat with Eva. Tune in to the last part of our interview where we find out about Eva's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker.Check out Guest’s links:Website https://invisiblenotbroken.com/humancare-podcastLinkedIn: https://www.linkedin.com/in/evalana/Facebook: https://www.facebook.com/elminkoff/Instagram: https://www.instagram.com/wellacopia/Youtube: https://www.youtube.com/channel/UCVOuHrKlIePZ61JBcel7dXg Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com Want to WIN $100? Just leave a review on iTunes, and at the end of each month we’ll choose one person at random to win. Here are some prompts right now to help you figure out what to put: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Unsure how to leave a review on desktop and on a Phone? Click the links to learn more. We got you covered. (Android users may need to download the apple podcasts app
In this episode, you’ll learn more about fibromyalgia and hypermobility syndrome as we chat with Eva Minkoff about her diagnosis. The highs and the lows. Symptoms to medication to things she’s found to help her condition. In the next episode find out about how she has dedicated her life to fostering better healthcare relationships for better healthcare outcomes and quality of life, and started the Invisible Not Broken Network. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Guest’s links:Website https://invisiblenotbroken.com/humancare-podcastLinkedIn: https://www.linkedin.com/in/evalana/Facebook: https://www.facebook.com/elminkoff/Instagram: https://www.instagram.com/wellacopia/Youtube: https://www.youtube.com/channel/UCVOuHrKlIePZ61JBcel7dXg Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com Want to WIN $100? Just leave a review on iTunes, and at the end of each month we’ll choose one person at random to win. Here are some prompts right now to help you figure out what to put: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Unsure how to leave a review on desktop and on a Phone? Click the links to learn more. We got you covered. (Android users may need to download the apple podcasts app)
In this episode, you’ll learn Michael's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker.Check out Guest’s links:http://www.mjwentink.com/https://twitter.com/mjwentinkhttps://www.instagram.com/mjwentink/https://www.facebook.com/michael.wentink.9https://themighty.com/2016/09/multiple-sclerosis-how-baking-gives-me-a-sense-of-order/https://themighty.com/2016/07/my-multiple-sclerosis-helped-me-view-work-in-a-new-light/ https://themighty.com/2016/06/my-multiple-sclerosis-helped-me-to-become-a-writer/ https://themighty.com/2016/09/how-i-found-my-voice-when-writing-about-my-multiple-sclerosis/ https://themighty.com/2014/11/when-mom-and-i-went-through-treatments-together/ Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com Want to WIN $100? Just leave a review on iTunes, and at the end of each month we’ll choose one person at random to win. Here are some prompts right now to help you figure out what to put: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Unsure how to leave a review on desktop and on a Phone? Click the links to learn more. We got you covered. (Android users may need to download the apple podcasts app)
In this episode, you’ll learn more about how he started to wrote about life with MS as we carry on our chat with Michael Wentink. Tune in to the last part of our interview where we find out about Michael's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Guest’s links:http://www.mjwentink.com/https://twitter.com/mjwentinkhttps://www.instagram.com/mjwentink/https://www.facebook.com/michael.wentink.9https://themighty.com/2016/09/multiple-sclerosis-how-baking-gives-me-a-sense-of-order/https://themighty.com/2016/07/my-multiple-sclerosis-helped-me-view-work-in-a-new-light/ https://themighty.com/2016/06/my-multiple-sclerosis-helped-me-to-become-a-writer/ https://themighty.com/2016/09/how-i-found-my-voice-when-writing-about-my-multiple-sclerosis/ https://themighty.com/2014/11/when-mom-and-i-went-through-treatments-together/ Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com Want to WIN $100? Just leave a review on iTunes, and at the end of each month we’ll choose one person at random to win. Here are some prompts right now to help you figure out what to put: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Unsure how to leave a review on desktop and on a Phone? Click the links to learn more. We got you covered. (Android users may need to download the apple podcasts app)
In this episode, you’ll learn more about Multiple Sclerosis as we chat with Michael Wentink about his diagnosis. The highs and the lows. Symptoms to medication to things she’s found to help his condition. In the next episode find out about how he medically retired and started writing Want to WIN a copy of our best selling ENabled Warrior Symptom Tracker? Enter the giveaway by going to www.mybookgiveaway.com to enter your details in Facebook messenger (lookout for a link that will pop up!) Or if you’re impatient (like me) and want yours now, Claim your discounted book from www.enabledwarriors.org/book Check out Guest’s links:http://www.mjwentink.com/https://twitter.com/mjwentinkhttps://www.instagram.com/mjwentink/https://www.facebook.com/michael.wentink.9https://themighty.com/2016/09/multiple-sclerosis-how-baking-gives-me-a-sense-of-order/https://themighty.com/2016/07/my-multiple-sclerosis-helped-me-view-work-in-a-new-light/ https://themighty.com/2016/06/my-multiple-sclerosis-helped-me-to-become-a-writer/ https://themighty.com/2016/09/how-i-found-my-voice-when-writing-about-my-multiple-sclerosis/ https://themighty.com/2014/11/when-mom-and-i-went-through-treatments-together/ Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com Want to WIN $100? Just leave a review on iTunes, and at the end of each month we’ll choose one person at random to win. Here are some prompts right now to help you figure out what to put: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Unsure how to leave a review on desktop and on a Phone? Click the links to learn more. We got you covered. (Android users may need to download the apple podcasts app)
In this episode, you’ll learn Natalie's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Guest’s links:Www.forthehealth.ca @for.the.health Listen to Jessie Ace (DISabled to ENabled podcast host) on Natalie’s ‘Sick and Successful’ podcast here: https://mmini.me/saspodcast Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com Want to WIN $100? Just leave a review on iTunes, and at the end of each month we’ll choose one person at random to win. Here are some prompts right now to help you figure out what to put: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Unsure how to leave a review on desktop and on a Phone? Click the links to learn more. We got you covered. (Android users may need to download the apple podcasts app)
In this episode, you’ll learn more about how she has put her condition into remission through diet and exercise as we carry on our chat with Natalie Suppes. Tune in to the last part of our interview where we find out about Natalie's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Guest’s links:Www.forthehealth.ca @for.the.health Listen to Jessie Ace (DISabled to ENabled podcast host) on Natalie’s ‘Sick and Successful’ podcast here: https://mmini.me/saspodcast Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com Want to WIN $100? Just leave a review on iTunes, and at the end of each month we’ll choose one person at random to win. Here are some prompts right now to help you figure out what to put: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Unsure how to leave a review on desktop and on a Phone? Click the links to learn more. We got you covered. (Android users may need to download the apple podcasts app)
In this episode, you’ll learn more about Crohn's and Ulcerative Colitis as we chat with Natalie Suppes about her diagnosis. The highs and the lows. Symptoms to medication to things she’s found to help her condition. In the next episode find out about how she became a holistic nutrition coach, breathwork practitioner and personal trainer despite her condition. Want to WIN a copy of our best selling ENabled Warrior Symptom Tracker? Enter the giveaway by going to www.mybookgiveaway.com to enter your details in Facebook messenger (lookout for a link that will pop up!) Or if you’re impatient (like me) and want yours now, Claim your discounted book from www.enabledwarriors.org/book Check out Guest’s links:Www.forthehealth.ca @for.the.health Listen to Jessie Ace (DISabled to ENabled podcast host) on Natalie’s ‘Sick and Successful’ podcast here: https://mmini.me/saspodcast Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com Want to WIN $100? Just leave a review on iTunes, and at the end of each month we’ll choose one person at random to win. Here are some prompts right now to help you figure out what to put: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Unsure how to leave a review on desktop and on a Phone? Click the links to learn more. We got you covered. (Android users may need to download the apple podcasts app)
In this episode, you’ll learn Claire's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Guest’s links:Blog: https://www.throughthefibrofog.com/Instagram: @through.the.fibro.fogInstagram food account: @lowhistaminekitchenTwitter: @throughfibrofogLiving through the fibro fog book - Amazon link Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com Want to WIN $100? Just leave a review on iTunes, and at the end of each month we’ll choose one person at random to win. Here are some prompts right now to help you figure out what to put: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Unsure how to leave a review on desktop and on a Phone? Click the links to learn more. We got you covered. (Android users may need to download the apple podcasts app)
In this episode, you’ll learn more about how she began Through The Fibro Fog and started her food Instagram as we carry on our chat with Claire. Tune in to the last part of our interview where we find out about Claire's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Guest’s links:Blog: https://www.throughthefibrofog.com/Instagram: @through.the.fibro.fogInstagram food account: @lowhistaminekitchenTwitter: @throughfibrofogLiving through the fibro fog book - Amazon link Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com Want to WIN $100? Just leave a review on iTunes, and at the end of each month we’ll choose one person at random to win. Here are some prompts right now to help you figure out what to put: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Unsure how to leave a review on desktop and on a Phone? Click the links to learn more. We got you covered. (Android users may need to download the apple podcasts app)
In this episode, you’ll learn more about dysautonomia, EDS, mast cell activation syndrome, vestibular and classic migraine, and interstitial cystitis as we chat with Claire about her diagnosis. The highs and the lows. Symptoms to medication to things she’s found to help her condition. In the next episode find out about her blogging, cooking and instagram advocacy! Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Guest’s links:Blog: https://www.throughthefibrofog.com/Instagram: @through.the.fibro.fogInstagram food account: @lowhistaminekitchenTwitter: @throughfibrofogLiving through the fibro fog book - Amazon link Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com Want to WIN $100? Just leave a review on iTunes, and at the end of each month we’ll choose one person at random to win. Here are some prompts right now to help you figure out what to put: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Unsure how to leave a review on desktop and on a Phone? Click the links to learn more. We got you covered. (Android users may need to download the apple podcasts app)
In this episode, you’ll learn Amanda's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Guest’s links:www.amandawebsterhealth.comInsta @amandawebsterhealth Self harm: www.selfharm.co.uk www.nshn.co.ukSuicide: call 116 123 www.samaritans.orgAddiciton: https://www.addiction.org.uk https://addictionhelplineamerica.com Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com Want to WIN $100? Just leave a review on iTunes, and at the end of each month we’ll choose one person at random to win. Here are some prompts right now to help you figure out what to put: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Unsure how to leave a review on desktop and on a Phone? Click the links to learn more. We got you covered. (Android users may need to download the apple podcasts app)
In this episode, you’ll learn more about how she proved her mental health professional wrong and went on to help others as we carry on our chat with Amanda Webster. Tune in on Friday for the last part of our interview where we find out about Amanda's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Guest’s links:www.amandawebsterhealth.comInsta @amandawebsterhealth Self harm: www.selfharm.co.uk www.nshn.co.ukSuicide: call 116 123 www.samaritans.orgAddiciton: https://www.addiction.org.uk https://addictionhelplineamerica.com Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com Want to WIN $100? Just leave a review on iTunes, and at the end of each month we’ll choose one person at random to win. Here are some prompts right now to help you figure out what to put: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Unsure how to leave a review on desktop and on a Phone? Click the links to learn more. We got you covered. (Android users may need to download the apple podcasts app)
In this episode we chat with Michael Wentink in San Antonio about what it's like to be in a COVID hotspot. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker.Connect with Michael:http://www.mjwentink.com/https://twitter.com/mjwentinkhttps://www.instagram.com/mjwentink/https://www.facebook.com/michael.wentink.9https://themighty.com/2016/09/multiple-sclerosis-how-baking-gives-me-a-sense-of-order/ https://themighty.com/2016/07/my-multiple-sclerosis-helped-me-view-work-in-a-new-light/ https://themighty.com/2016/06/my-multiple-sclerosis-helped-me-to-become-a-writer/ https://themighty.com/2016/09/how-i-found-my-voice-when-writing-about-my-multiple-sclerosis/ https://themighty.com/2014/11/when-mom-and-i-went-through-treatments-together/ Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled
In this episode, you’ll learn more about depression, addiction, self-harm and suicide as we chat with Amanda Webster about her experience. The highs and the lows. Symptoms to medication to things she’s found to help her condition. In the next episode find out about how she became a fitness model and wellness coach. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Guest’s links:www.amandawebsterhealth.comInsta @amandawebsterhealth Self harm: www.selfharm.co.uk www.nshn.co.ukSuicide: call 116 123 www.samaritans.orgAddiciton: https://www.addiction.org.uk https://addictionhelplineamerica.com Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com Want to WIN $100? Just leave a review on iTunes, and at the end of each month we’ll choose one person at random to win. Here are some prompts right now to help you figure out what to put: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Unsure how to leave a review on desktop and on a Phone? Click the links to learn more. We got you covered. (Android users may need to download the apple podcasts app)
In this episode, you’ll learn Daralyse's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast! The podcast for people with chronic illnesses. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Guest’s links: www.daralyselyons.com https://www.youtube.com/channel/UCqAEPNoJUSd3Nfoq0MXtfdg https://www.facebook.com/TheTransformationalStoryteller/ https://twitter.com/daralyselyons https://www.instagram.com/daralyselyons/ Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors IG: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com Want to WIN $100? Just leave a review on iTunes, and at the end of each month we’ll choose one person at random to win. Here are some prompts right now to help you figure out what to put: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Unsure how to leave a review on desktop and on a Phone? Click the links to learn more. We got you covered. (Android users may need to download the apple podcasts app)
In this episode, you’ll learn more about overcoming her illness and becoming a transformational coach as we carry on our chat with Daralyse Lyons. Tune in to the last part of our interview where we find out about Daralyse's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Guest’s links: www.daralyselyons.com https://www.youtube.com/channel/UCqAEPNoJUSd3Nfoq0MXtfdg https://www.facebook.com/TheTransformationalStoryteller/ https://twitter.com/daralyselyons https://www.instagram.com/daralyselyons/ Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com Want to WIN $100? Just leave a review on iTunes, and at the end of each month we’ll choose one person at random to win. Here are some prompts right now to help you figure out what to put: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Unsure how to leave a review on desktop and on a Phone? Click the links to learn more. We got you covered. (Android users may need to download the apple podcasts app)
In this episode, we chat with Eva Minkoff in New York (the state, not the city!) about her month under lockdown in the Big Apple and her ties to the medical world. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Guest’s links:Website: https://invisiblenotbroken.com/humancare-podcastLinkedIn: https://www.linkedin.com/in/evalana/Facebook: https://www.facebook.com/elminkoff/Instagram: https://www.instagram.com/wellacopia/Youtube: https://www.youtube.com/channel/UCVOuHrKlIePZ61JBcel7dXg Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com Want to WIN a copy of our best selling ENabled Warrior Symptom Tracker that we created to help you track and manage your symptoms, spot triggers and get the best treatment from your doctors? Enter the giveaway by going to www.mybookgiveaway.com and enter your details through Facebook messenger (lookout for a link that will pop up!) Or if you’re impatient (like me) and want yours now, Claim your discounted book from www.enabledwarriors.org/book
In this episode, you’ll learn more about bulimia and eating disorders as we chat with Daralyse Lyons about her diagnosis. The highs and the lows. Symptoms to medication to things she’s found to help her condition. In the next episode find out about how she thrives as an author, actress, yogi, and transformational coach/speaker and podcast host! Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Guest’s links: www.daralyselyons.com https://www.youtube.com/channel/UCqAEPNoJUSd3Nfoq0MXtfdg https://www.facebook.com/TheTransformationalStoryteller/ https://twitter.com/daralyselyons https://www.instagram.com/daralyselyons/ Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com Want to WIN $100? Just leave a review on iTunes, and at the end of each month we’ll choose one person at random to win. Here are some prompts right now to help you figure out what to put: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Unsure how to leave a review on desktop and on a Phone? Click the links to learn more. We got you covered. (Android users may need to download the apple podcasts app)
In this episode, you’ll learn Amy's not-so-super-quick secrets. You’ll discover their favourite book, place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Amy's links:'But you don't look ill page' on Facebook 'MS Together' MS Support group@butyoudontlookill on Instagram @mstogetherofficial on Instagram for the MS Support group https://www.justgiving.com/fundraising/amy-thompson52 - Marathon JustGiving page Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com Want to WIN $100? Just leave a review on iTunes, and at the end of each month we’ll choose one person at random to win. Here are some prompts right now to help you figure out what to put: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Unsure how to leave a review on desktop and on a Phone? Click the links to learn more. We got you covered. (Android users may need to download the apple podcasts app)
In this episode, you’ll learn more about her blog, support group and marathon training as we carry on our chat with Amy Thompson. Tune in to the last part of our interview where we find out about Amy's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker.Amy's links:'But you don't look ill page' on Facebook 'MS Together' MS Support group@butyoudontlookill on Instagram @mstogetherofficial on Instagram for the MS Support group https://www.justgiving.com/fundraising/amy-thompson52 - Marathon JustGiving page Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com
In this episode we chat with Natalie Suppes to find out how it's been to be pregnant during a pandemic! Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Guest’s links:Www.forthehealth.ca @for.the.health Listen to Jessie Ace (DISabled to ENabled podcast host) on Natalie’s ‘Sick and Successful’ podcast here: https://mmini.me/saspodcast Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comGet your FREE 7 chronic illness hacks doctors never tell you here. Want to WIN a copy of our best selling ENabled Warrior Symptom Tracker that we created to help you track and manage your symptoms, spot triggers and get the best treatment from your doctors? Enter the giveaway by going to www.mybookgiveaway.com and enter your details through Facebook messenger (lookout for a link that will pop up!) Or if you’re impatient (like me) and want yours now, Claim your discounted book from www.enabledwarriors.org/book
In this episode, you’ll learn more about Multiple Sclerosis as we chat with Amy Thompson about her diagnosis. The highs and the lows. Symptoms to medication to things she’s found to help her condition. In the next episode find out about how she has since skydived, trained for a marathon and set up her blog and support group for others in similar situations. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Amy's links:'But you don't look ill page' on Facebook 'MS Together' MS Support group@butyoudontlookill on Instagram @mstogetherofficial on Instagram for the MS Support group https://www.justgiving.com/fundraising/amy-thompson52 - Marathon JustGiving page Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com Want to WIN $100? Just leave a review on iTunes, and at the end of each month we’ll choose one person at random to win. Here are some prompts right now to help you figure out what to put: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Unsure how to leave a review on desktop and on a Phone? Click the links to learn more. We got you covered. (Android users may need to download the apple podcasts app)
In this episode, you’ll learn Courtney's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Courtney's links:https://www.hopeforataxia.org/Facebook: https://www.facebook.com/hopeforataxia/Twitter: https://twitter.com/hopeforataxiaInstagram: @hopeforataxiaFaces of Ataxia: https://www.hopeforataxia.org/faces-of-ataxia/Burpee Challenge Fundraiser: https://www.canadahelps.org/en/charities/ataxia-canada/p2p/ataxiaburpeechallenge/Links to register for our weekly support groups every Friday at 3 and 6PM EST: hopeforataxia.org/6pm and hopeforataxia.org/3pm Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com Want to WIN $100? Just leave a review on iTunes, and at the end of each month we’ll choose one person at random to win. Here are some prompts right now to help you figure out what to put: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Unsure how to leave a review on desktop and on a Phone? Click the links to learn more. We got you covered. (Android users may need to download the apple podcasts app)
In this episode, you’ll learn more about Hope for Ataxia and the Ataxia Burpee Challenge as we carry on our chat with Courtney. Tune in to the last part of our interview where we find out about Courtney's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Courtney's links:https://www.hopeforataxia.org/Facebook: https://www.facebook.com/hopeforataxia/Twitter: https://twitter.com/hopeforataxiaInstagram: @hopeforataxiaFaces of Ataxia: https://www.hopeforataxia.org/faces-of-ataxia/Burpee Challenge Fundraiser: https://www.canadahelps.org/en/charities/ataxia-canada/p2p/ataxiaburpeechallenge/Links to register for our weekly support groups every Friday at 3 and 6PM EST: hopeforataxia.org/6pm and hopeforataxia.org/3pm Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com Want to WIN $100? Just leave a review on iTunes, and at the end of each month we’ll choose one person at random to win. Here are some prompts right now to help you figure out what to put: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Unsure how to leave a review on desktop and on a Phone? Click the links to learn more. We got you covered. (Android users may need to download the apple podcasts app)
Today we have another special blooper episode! Despite what you may think, not everything comes out perfectly first time round. Which means you get to listen to some of these hilarious and relatable bloopers. Enjoy and stay ENabled! Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comGet your FREE 7 chronic illness hacks doctors never tell you here. Want to WIN a copy of our best selling ENabled Warrior Symptom Tracker that we created to help you track and manage your symptoms, spot triggers and get the best treatment from your doctors? Enter the giveaway by going to www.mybookgiveaway.com and enter your details through Facebook messenger (lookout for a link that will pop up!) Or if you’re impatient (like me) and want yours now, Claim your discounted book from www.enabledwarriors.org/book
In this episode, you’ll learn more about Autosomal Reccessive Cerebellar Ataxia Type 1 as we chat with Courtney Ng about her diagnosis. The highs and the lows. Symptoms to medication to things she’s found to help her condition. In the next episode, find out about how she worked with her friend Mark to develop Faces of Ataxia and the Ataxia Burpee Challenge. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Courtney's links:https://www.hopeforataxia.org/Facebook: https://www.facebook.com/hopeforataxia/Twitter: https://twitter.com/hopeforataxiaInstagram: @hopeforataxiaFaces of Ataxia: https://www.hopeforataxia.org/faces-of-ataxia/Burpee Challenge Fundraiser: https://www.canadahelps.org/en/charities/ataxia-canada/p2p/ataxiaburpeechallenge/Links to register for our weekly support groups every Friday at 3 and 6PM EST: hopeforataxia.org/6pm and hopeforataxia.org/3pm Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com Want to WIN $100? Just leave a review on iTunes, and at the end of each month we’ll choose one person at random to win. Here are some prompts right now to help you figure out what to put: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Unsure how to leave a review on desktop and on a Phone? Click the links to learn more. We got you covered. (Android users may need to download the apple podcasts app)
In the next and final episode, discover some behind the scenes movie magic and how they create prop drugs for actors! Missed Edward’s other two episodes? Make sure to check those out right now so you know what we’re talking about. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Edward’s links:Learn more about the documentary here: https://www.imdb.com/title/tt4023464/Connect with Edward on Instagram @an_anti_hero_productionRent the documentary here: https://vimeo.com/ondemand/ourfriendjon/407029487 Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com Want to WIN $100? Just leave a review on iTunes, and at the end of each month we’ll choose one person at random to win. Here are some prompts right now to help you figure out what to put: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Unsure how to leave a review on desktop and on a Phone? Click the links to learn more. We got you covered. (Android users may need to download the apple podcasts app)
In this episode, we learn the ins and outs of how to make a documentary film. How did he manage to make a film about a friend who’d just passed away? In the next and final episode, discover some behind the scenes movie magic and how they create prop drugs for actors! Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker.Check out Edward’s links:Learn more about the documentary here: https://www.imdb.com/title/tt4023464/Connect with Edward on Instagram @an_anti_hero_productionRent the documentary here: https://vimeo.com/ondemand/ourfriendjon/407029487 Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com Want to WIN $100? Just leave a review on iTunes, and at the end of each month we’ll choose one person at random to win. Here are some prompts right now to help you figure out what to put: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Unsure how to leave a review on desktop and on a Phone? Click the links to learn more. We got you covered. (Android users may need to download the apple podcasts app)
In this episode we chat with Amanda Webster in Arizona to find out how she's not bored and more connected! Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Guest’s links:www.amandawebsterhealth.comInsta @amandawebsterhealth Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com
In this episode, you’ll learn about how today’s guest helped create a film about his friend Jon who passed away from Sickle Cell Anemia using Jon’s friends as the cast and crew! In this episode, we find out more about Jon and what he stood for in his fight against Sickle Cell. In the next episode, we learn the ins and outs of how to make a documentary film. How did he manage to make a film about a friend who’d just passed away? Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker.Check out Edward’s links:Learn more about the documentary here: https://www.imdb.com/title/tt4023464/Connect with Edward on Instagram @an_anti_hero_productionRent the documentary here: https://vimeo.com/ondemand/ourfriendjon/407029487 Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com Want to WIN $100? Just leave a review on iTunes, and at the end of each month we’ll choose one person at random to win. Here are some prompts right now to help you figure out what to put: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Unsure how to leave a review on desktop and on a Phone? Click the links to learn more. We got you covered. (Android users may need to download the apple podcasts app)
In this episode, you’ll learn Carley's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Carley's links:Peonyhc.comInsta + twitter @peony_hcFb https://www.facebook.com/peonyhcJoin our tribe of ENabled warriors who fight back against chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled
In this episode, you’ll learn more about Peony Health Coordination and helping others manage the stress and organisation that comes with chronic illness as we carry on our chat with Carley Gordon. Tune in to the last part of our interview where we find out about Carley's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Carley's links:Peonyhc.comInsta + twitter @peony_hcFb https://www.facebook.com/peonyhc Join our tribe of ENabled warriors who fight back against chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled twitter @DISabletoenable
In this episode we chat with Daralyse Lyons to find out how her social life has changed during the pandemic. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Guest links: www.daralyselyons.com https://www.youtube.com/channel/UCqAEPNoJUSd3Nfoq0MXtfdg https://www.facebook.com/TheTransformationalStoryteller/ https://twitter.com/daralyselyons https://www.instagram.com/daralyselyons/ Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com
In this episode, you’ll learn more about Hyperadrenergic P.O.T.S., MCAS and EDS type III as we chat with Carley Gordon about her diagnosis. The highs and the lows. Symptoms to medication to things she’s found to help his condition. In the next episode find out about how she started Peony Health Coordination to help others manage their appointments in the limbo-land and confusion of chronic illness. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Carley's links:Peonyhc.comInsta + twitter @peony_hcFb https://www.facebook.com/peonyhc Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled
In this episode, you’ll learn Lori's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Lori's links:- https://ladpdjourney2.wordpress.com- https://parkinsonsnewstoday.com/author/lori-deporter/https://www.epda.eu.com/latest/news/boxing-coach-and-writer-shares-early-onset-parkinsons-experience/- https://wetakeonlondon.wordpress.com- https://aloha25yrs.tumblr.com/- https://tuscansun2016.tumblr.com/- https://lorideporter.issacertifiedtrainer.com/Also, check out Jessie Ace’s column for BioNews Services via Multiple Sclerosis News Today Join our tribe of ENabled warriors who fight back against chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled
In this episode, you’ll learn more about becoming a boxing coach and learning to tango as we carry on our chat with Lori. Tune in to the last part of our interview on Friday where we find out about Lori's not-so-super-quick secrets. You’ll discover her favourite book, favourite place, scariest thing she's done and (our favourite) the weirdest thing. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast.Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Lori's links:- https://ladpdjourney2.wordpress.com- https://parkinsonsnewstoday.com/author/lori-deporter/- https://www.epda.eu.com/latest/news/boxing-coach-and-writer-shares-early-onset-parkinsons-experience/- https://lorideporter.issacertifiedtrainer.com/ Also, check out Jessie Ace’s column for BioNews Services via Multiple Sclerosis News Today Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled
In this episode we chat with Amy Thompson and how she's been able to take her support group online during the pandemic. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Guest links:'But you don't look ill page' on Facebook 'MS Together' MS Support group@butyoudontlookill on Instagram @mstogetherofficial on Instagram for the MS Support group https://www.justgiving.com/fundraising/amy-thompson52 - Marathon JustGiving page Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled
In this episode, you’ll learn more about young-onset Parkinson's as we chat with Lori DePorter about her diagnosis. The highs and the lows. Symptoms to medication to things she’s found to help her condition. In the next episode find out about how she became a personal trainer and started writing for Parkinson's News Today. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Lori's links:- https://ladpdjourney2.wordpress.com- https://parkinsonsnewstoday.com/author/lori-deporter/- https://www.epda.eu.com/latest/news/boxing-coach-and-writer-shares-early-onset-parkinsons-experience/- https://wetakeonlondon.wordpress.com- https://aloha25yrs.tumblr.com/- https://tuscansun2016.tumblr.com/- https://lorideporter.issacertifiedtrainer.com/Also, check out Jessie Ace’s column for BioNews Services via Multiple Sclerosis News Today Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled
In this episode, you’ll learn Dr. Lynette's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Lynette's links:www.lynettelouise.comwww.brainbody.nethttps://www.facebook.com/lynette.louise.7https://www.facebook.com/lynette.louise1https://www.facebook.com/Miracles-Are-Made-a-real-life-guide-to-Autism-195612530483540/https://www.facebook.com/thebrainbroad/https://twitter.com/lynettelouisehttps://www.linkedin.com/in/lynette-louise-the-brain-broad-4aa8291/https://www.instagram.com/the_brain_broad/ Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled Get the written out version of the episodes here: https://mmini.me/transcription
In this episode, you’ll learn more about travel therapy, neurofeedback and her autism docuseries as we carry on our chat with Dr. Lynette Louise. Tune in to the last part of our interview on Friday where we find out about Dr. Lynette's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Lynette's links:www.lynettelouise.comwww.brainbody.nethttps://www.facebook.com/lynette.louise.7 https://www.facebook.com/lynette.louise1https://www.facebook.com/Miracles-Are-Made-a-real-life-guide-to-Autism-195612530483540/https://www.facebook.com/thebrainbroad/https://twitter.com/lynettelouisehttps://www.linkedin.com/in/lynette-louise-the-brain-broad-4aa8291/https://www.instagram.com/the_brain_broad/ Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled
In this episode, we chat with Courtney Ng in Canada. She talks to us about the importance of online community for people who are isolated with Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Follow Courtney's links:https://www.hopeforataxia.org/Facebook: https://www.facebook.com/hopeforataxia/Twitter: https://twitter.com/hopeforataxiaInstagram: @hopeforataxiaFaces of Ataxia: https://www.hopeforataxia.org/faces-of-ataxia/Burpee Challenge Fundraiser: https://www.canadahelps.org/en/charities/ataxia-canada/p2p/ataxiaburpeechallenge/Links to register for our weekly support groups every Friday at 3 and 6PM EST: hopeforataxia.org/6pm and hopeforataxia.org/3pm Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled Get the written out version of the episodes here: https://mmini.me/transcription
In this episode, you’ll learn more about Autism as we chat with Dr. Lynette Louise about her children and the diagnosis. The highs and the lows. Symptoms to medication to things she’s found to help the condition. In the next episode find out about how she harnessed travel therapy, neurofeedback and spread her research and expertise. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Lynette's links:www.lynettelouise.comwww.brainbody.nethttps://www.facebook.com/lynette.louise.7 https://www.facebook.com/lynette.louise1https://www.facebook.com/Miracles-Are-Made-a-real-life-guide-to-Autism-195612530483540/https://www.facebook.com/thebrainbroad/https://twitter.com/lynettelouisehttps://www.linkedin.com/in/lynette-louise-the-brain-broad-4aa8291/https://www.instagram.com/the_brain_broad/ Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled Get the written out version of the episodes here: https://mmini.me/transcription
In this episode, you’ll learn Natalie's not-so-super-quick secrets. You’ll discover her favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Natalie's links:https://thechargimals.comHttps://theunchargeablesshop.comHttps://theunchargeables.comwww.facebook.com/theunchargeables Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled Get the written out version of the episodes here: https://mmini.me/transcription
In this episode, you’ll learn more about how Natalie created the Unchargeables movement and dreamt up the Chargimals as we carry on our chat with Natalie. Tune in to the last part of our interview where we find out about Natalie's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Check out Natalie's links:https://thechargimals.comHttps://theunchargeablesshop.comHttps://theunchargeables.comwww.facebook.com/theunchargeables Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled Get the written out version of the episodes here: https://mmini.me/transcription
In this episode, we chat with Edward Payson in California. He talks to us about the intimacy that lockdown has brought as we are forced to drop any pretenses of public image. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Learn more about the documentary here: https://www.imdb.com/title/tt4023464/Connect with Edward on Instagram @an_anti_hero_productionRent the documentary here: https://vimeo.com/ondemand/ourfriendjon/407029487 Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comGet your FREE 7 chronic illness hacks doctors never tell you here. WIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts app Get the written out version of the episodes here: https://mmini.me/transcription
In this episode, you’ll learn more about Fibromyalgia, Hashimoto's Disease, Celiac Disease, Raynaud's disease, and Cold Urticaria as we chat with Natalie about her diagnosis. The highs and the lows. Symptoms to medication to things she’s found to help her condition. In the next episode find out about how she started the Unchargeables and the Chargimals! Please note our giveaway is now closedYou can still claim your book on AmazonSearch ENabled Warrior Tracker. Check out Natalie's links:https://thechargimals.comHttps://theunchargeablesshop.comHttps://theunchargeables.comwww.facebook.com/theunchargeables Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledGet the written out version of the episodes here: https://mmini.me/transcription
This week we have a 5 episode special with returning guest, Jess Faulds.In this 5th and final episode, we're back with Jess to hear about how she coped with chemotherapy. We also have MORE not-so-super-quick-secrets from Jess! Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Follow Jess here:www.alltherightbites.cafb/IG @AlltheRightBites Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled Get the written out version of the episodes here: https://mmini.me/transcription
This week we have a 5 episode special with returning guest, Jess Faulds.In this 4th episode, Jess tells us about documenting her experiences on Instagram.Make sure you listen to the next episode to find out how Jess coped with chemotherapy. We also have MORE not-so-super-quick-secrets! Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Follow Jess here:www.alltherightbites.cafb/IG @AlltheRightBites Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled Get the written out version of the episodes here: https://mmini.me/transcription
This week we have a 5 episode special with returning guest, Jess Faulds.In this 3rd episode, Jess discusses her experience with menopause in her late twenties, after undergoing HSCT.Make sure you listen to the next 2 episodes to find out about Jess's experiences of documenting her journey on Instagram and coping with chemotherapy. We also have MORE not-so-super-quick-secrets! Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Follow Jess here:www.alltherightbites.cafb/IG @AlltheRightBites Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comGet your FREE 7 chronic illness hacks doctors never tell you here. WIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts app Get the written out version of the episodes here: https://mmini.me/transcription
This week we have a 5 episode special with returning guest, Jess Faulds.In this 2nd episode, we're back with Jess as she talks about freezing her eggs at just 28 years old.Make sure you listen to the next 3 episodes to find out about Jess's experiences with menopause, documenting her journey on Instagram, and coping with chemotherapy. We also have MORE not-so-super-quick-secrets! Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Follow Jess here:www.alltherightbites.cafb/IG @AlltheRightBites Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled Get the written out version of the episodes here: https://mmini.me/transcription
This week we have a 5 episode special with returning guest, Jess Faulds.In this 1st episode, we're back with Jess to hear about her experience with Hematopoietic Stem Cell Transplantation, to treat MS.Make sure you listen to the next 4 episodes to find out about Jess's experiences with freezing her eggs, menopause, documenting her journey on Instagram, and coping with chemotherapy. We also have MORE not-so-super-quick-secrets! Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Follow Jess here:www.alltherightbites.cafb/IG @AlltheRightBites Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled Get the written out version of the episodes here: https://mmini.me/transcription
In this episode, you’ll learn Lisa's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Check out Lisa's links:"Keep Shining" youtube video:https://youtu.be/4wYJcnCvhyo My book:https://www.amazon.com/Light-Darkness-Lisa-Sniderman/dp/1681605570/ My websites and social media sites:alightinthedarkness.infodoyoubelieveinmagic.infowhataredreamsmadeof.comisloveafairytale.comaoedemuse.comfacebook.com/aoedemusemusictwitter.com/aoedemuseyoutube.com/aoedemuseHow to Thrive Facebook group: https://www.facebook.com/groups/2521920814702414/ Lights in the Darkness-Artists, Authors, Musicians Creating to Heal-Facebook Group:https://www.facebook.com/groups/433332727132078/ Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled Get the written out version of the episodes here: https://mmini.me/transcription
In this episode, you’ll learn more about using the creative arts to heal as we carry on our chat with Lisa Sniderman. Tune in to the last part of our interview where we find out about Lisa's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Check out Lisa's links"Keep Shining" youtube video:https://youtu.be/4wYJcnCvhyo My book:https://www.amazon.com/Light-Darkness-Lisa-Sniderman/dp/1681605570/ My websites and social media sites: alightinthedarkness.infodoyoubelieveinmagic.infowhataredreamsmadeof.comisloveafairytale.comaoedemuse.comfacebook.com/aoedemusemusictwitter.com/aoedemuseyoutube.com/aoedemuseHow to Thrive Facebook group:https://www.facebook.com/groups/2521920814702414/ Lights in the Darkness-Artists, Authors, Musicians Creating to Heal-Facebook Group:https://www.facebook.com/groups/433332727132078/ Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled Get the written out version of the episodes here: https://mmini.me/transcription
In this episode, we chat with Carley Gordon in Chicago, Illinois. She tells us about things reopening around her and how she's been able to escape to the suburbs. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Check out Carley's linksPeonyhc.comInsta + twitter @peony_hcFb https://www.facebook.com/peonyhc Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled Get the written out version of the episodes here: https://mmini.me/transcription
In this episode, you’ll learn more about Dermatomyositis as we chat with Lisa Sniderman about her diagnosis. The highs and the lows. Symptoms to medication to things she’s found to help her condition. In the next episode find out about how she has been using creativity to heal. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Check out Lisa's links"Keep Shining" youtube video:https://youtu.be/4wYJcnCvhyo My book:https://www.amazon.com/Light-Darkness-Lisa-Sniderman/dp/1681605570/ My websites and social media sites:alightinthedarkness.infodoyoubelieveinmagic.infowhataredreamsmadeof.comisloveafairytale.comaoedemuse.com facebook.com/aoedemusemusic twitter.com/aoedemuse youtube.com/aoedemuse How to Thrive Facebook group:https://www.facebook.com/groups/2521920814702414/ Lights in the Darkness-Artists, Authors, Musicians Creating to Heal-Facebook Group:https://www.facebook.com/groups/433332727132078/ Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled Get the written out version of the episodes here: https://mmini.me/transcription
In this episode, you’ll learn Daniele's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Check out Daniele's linkshttps://diabetesdominator.com/ www.lovemcm.com https://www.facebook.com/diabetesdominator/ https://twitter.com/diabetesDomin8r https://www.instagram.com/diabetesdominator/ https://www.linkedin.com/in/danielehargenrader/ Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled Get the written out version of the episodes here: https://mmini.me/transcription
In this episode, you’ll learn more about Diabetes Dominator and coaching others as we carry on our chat with Daniele Hargenrader.Tune in to the last part of our interview where we find out about Daniele's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Check out Daniele's links:https://diabetesdominator.com/ www.lovemcm.com https://www.facebook.com/diabetesdominator/ https://twitter.com/diabetesDomin8r https://www.instagram.com/diabetesdominator https://www.linkedin.com/in/danielehargenrader/ Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled Get the written out version of the episodes here: https://mmini.me/transcription
In this COVID 19 Special episode, we chat with Lori DePorter in Pennsylvania. She talks to us about the impact that the pandemic has had on children and young people, and how the Queen of the Castle no longer has an empty nest. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Check out Lori's linkshttps://ladpdjourney2.wordpress.com- https://parkinsonsnewstoday.com/author/lori-deporter/https://www.epda.eu.com/latest/news/boxing-coach-and-writer-shares-early-onset-parkinsons-experience/- https://wetakeonlondon.wordpress.com- https://aloha25yrs.tumblr.com/- https://tuscansun2016.tumblr.com/- https://lorideporter.issacertifiedtrainer.com/Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comGet your FREE 7 chronic illness hacks doctors never tell you here. WIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts app Get the written out version of the episodes here: https://mmini.me/transcription
In this episode, you’ll learn more about Diabetes as we chat with Daniele about her diagnosis. The highs and the lows. Symptoms to medication to things she’s found to help her condition. In the next episode find out about Diabetes Dominator and coaching others. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Check out Daniele's linkshttps://diabetesdominator.com/ www.lovemcm.com https://www.facebook.com/diabetesdominator/ https://twitter.com/diabetesDomin8r https://www.instagram.com/diabetesdominator/ https://www.linkedin.com/in/danielehargenrader/ Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled Get the written out version of the episodes here: https://mmini.me/transcription
In this episode, you’ll learn Brad's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Check out Brad's linkshttps://cysticfibrosisnewstoday.com/category/victorious-a-column-by-brad-dell/https://www.instagram.com/coffee.cats_/https://www.facebook.com/AdamantiumJoy/?ref=bookmarkshttps://twitter.com/braddellGet your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Join our tribe of ENabled warriors who fight back against chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled Get the written out version of the episodes here: https://mmini.me/transcription
In this episode, you’ll learn more about writing to help others through lung transplantation, cystic fibrosis and deafness as we carry on our chat with Brad Dell. Tune in to the last part of our interview where we find out about Brad's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Check out Brad's linkshttps://cysticfibrosisnewstoday.com/category/victorious-a-column-by-brad-dell/https://www.instagram.com/coffee.cats_/https://www.facebook.com/AdamantiumJoy/?ref=bookmarkshttps://twitter.com/braddell Join our tribe of ENabled warriors who fight back against chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled twitter @DISabletoenableGet the written out version of the episodes here: https://mmini.me/transcription
In this COVID 19 Special episode, we chat with Dr. Lynette Louise in California. She tells us about homeschooling and gives some tips for parents that have had to turn their hand to teaching during the pandemic. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Check out Lynette's links:www.lynettelouise.com www.brainbody.net https://www.facebook.com/lynette.louise.7 https://www.facebook.com/lynette.louise1https://www.facebook.com/Miracles-Are-Made-a-real-life-guide-to-Autism-195612530483540/https://www.facebook.com/thebrainbroad/https://twitter.com/lynettelouisehttps://www.linkedin.com/in/lynette-louise-the-brain-broad-4aa8291/https://www.instagram.com/the_brain_broad/ Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.com Get the written out version of the episodes here: https://mmini.me/transcription
In this episode, we chat with Brad Dell about cystic fibrosis, lung transplantation, and deafness, and writing to help others. Learn more about Brad's experiences and the amazing things he's done despite his illness on the DISabled to ENabled podcast this week. In this episode, you’ll learn more about cystic fibrosis, lung transplantation and deafness as we chat with Brad Dell about his diagnosis. The highs and the lows. Symptoms to medication to things she’s found to help his condition. In the next episode find out about how he went on to write about his experiences to help others. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Check out Brad's links https://cysticfibrosisnewstoday.com/category/victorious-a-column-by-brad-dell/https://www.instagram.com/coffee.cats_/https://www.facebook.com/AdamantiumJoy/https://twitter.com/braddell Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comGet the written out version of the episodes here: https://mmini.me/transcription
In this episode, you’ll learn Jameisha's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Check out Jameisha's linksWebsite www.youlookokaytome.comInstagram: https://www.instagram.com/youlookokaytome/Twitter: https://twitter.com/YouLookOkayToMeFacebook: https://www.facebook.com/youlookokaytome/YouTube: https://www.youtube.com/channel/UC33MjJJGFWayn6pMDxoa-gQGet your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Join our tribe of ENabled warriors who fight back against chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledGet your FREE 7 chronic illness hacks doctors never tell you here. Follow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comWIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts app Get the written out version of the episodes here: https://mmini.me/transcription
Today we have another special blooper episode! Despite what you may think, not everything comes out perfectly first time round. Which means you get to listen to some of these hilarious and relatable bloopers. Enjoy and stay ENabled! Join our tribe of ENabled warriors who fight back against their symptoms!:Facebook / ENabled Warriors Insta: @ DISabledtoENabled twitter @DISabletoenableWant to tips for managing your symptoms? Check out our blog: www.DISabledtoENabled.com Get your ENabled Warrior Tracker HERE today!Enter to WIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts app
In this episode, you’ll learn more about filmmaking, working at the BBC and navigating the Personal Independence Payment applications process as we carry on our chat with Jameisha Prescod. Tune in to the last part of our interview where we find out about Jameisha's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Check out Jameisha's linksWebsite www.youlookokaytome.comInstagram: https://www.instagram.com/youlookokaytome/Twitter: https://twitter.com/YouLookOkayToMeFacebook: https://www.facebook.com/youlookokaytome/YouTube: https://www.youtube.com/channel/UC33MjJJGFWayn6pMDxoa-gQ Join our tribe of ENabled warriors who fight back against chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled twitter @DISabletoenableGet your FREE 7 chronic illness hacks doctors never tell you here. Follow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comWIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts appGet the written out version of the episodes here: https://mmini.me/transcription
In this COVID 19 Special episode, we chat with Natalie Van Scheltinga about living in lockdown in the Canary Island, under Spanish regulations. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Check out Natalie's links:https://thechargimals.comHttps://theunchargeablesshop.comHttps://theunchargeables.comwww.facebook.com/theunchargeables www.instagram.com/theunchargeableswww.facebook.com/thechargimals www.instagram.com/thechargimals Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comGet your FREE 7 chronic illness hacks doctors never tell you here. WIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts app
In this episode, you’ll learn more about Lupus as we chat with Jameisha Prescod about her diagnosis. The highs and the lows. Symptoms to medication to things she’s found to help her condition. In the next episode find out about You Look Okay To Me and filmmaking. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Check out Jameisha's linksWebsite www.youlookokaytome.comInstagram: https://www.instagram.com/youlookokaytome/Twitter: https://twitter.com/YouLookOkayToMeFacebook: https://www.facebook.com/youlookokaytome/YouTube: https://www.youtube.com/channel/UC33MjJJGFWayn6pMDxoa-gQ Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comGet your FREE 7 chronic illness hacks doctors never tell you here. WIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts appGet the written out version of the episodes here: https://mmini.me/transcription
In this episode, you’ll learn Ardra's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Check out Ardra's linkshttps://trippingonair.com/https://www.facebook.com/trippingonair/https://www.instagram.com/ms_trippingonair/https://twitter.com/tripping_onairhttps://youtu.be/wW7yXFp563A Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Join our tribe of ENabled warriors who fight back against chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledGet your FREE 7 chronic illness hacks doctors never tell you here. Follow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comWIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts appGet the written out version of the episodes here: https://mmini.me/transcription
Today we have a special blooper episode! Despite what you may think, not everything comes out perfectly first time round. Which means you get to listen to some of these hilarious and relatable bloopers. Enjoy and stay ENabled! Join our tribe of ENabled warriors who fight back against their symptoms!:Facebook / ENabled Warriors Insta: @ DISabledtoENabled twitter @DISabletoenableWant to tips for managing your symptoms? Check out our blog: www.DISabledtoENabled.com Get your ENabled Warrior Tracker HERE today!Enter to WIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts app
In this episode, we chat with Ardra Shephard about MS and becoming a devastating illness expert and blogger. Learn more about MS and the amazing things she's done despite it on the DISabled to ENabled podcast this week. Keep up with Ardra:https://trippingonair.com/https://www.facebook.com/trippingonair/https://www.instagram.com/ms_trippingonair/https://twitter.com/tripping_onairhttps://youtu.be/wW7yXFp563A Join our tribe of ENabled warriors who fight back against their symptoms!:Facebook / ENabled Warriors Insta: @ DISabledtoENabled twitter @DISabletoenableWant to tips for managing your symptoms? Check out our blog: www.DISabledtoENabled.com Join the VIP waitlist to get the ENabled Warrior Tracker before anyone else click here to join through Facebook Messenger: http://mmini.me/waitlistEnter to WIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts app ENabled warriors thank you for supporting our sponsors. Today's episode is sponsored by BeeKeeper's Naturals. Start building your natural first aid kit today. Use code WARRIOR for 10% off your order.Read the transcription of the episodes here: https://mmini.me/transcription
In this COVID 19 Special episode, we chat with Jess Faulds in Canada, who recently underwent HSCT for her MS. We find out how she's coping with distancing whilst being immunocompromised. Follow Jess!www.alltherightbites.caInstagram: @alltherightbites Join our tribe of ENabled warriors who fight back against their symptoms!:Facebook / ENabled Warriors Insta: @ DISabledtoENabled twitter @DISabletoenableWant to tips for managing your symptoms? Check out our blog: www.DISabledtoENabled.com Join the VIP waitlist to get the ENabled Warrior Tracker before anyone else click here to join through Facebook Messenger: http://mmini.me/waitlistEnter to WIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts app
In this episode, we chat with Ardra Shephard about MS and becoming a devastating illness expert and blogger. Learn more about MS and the amazing things she's done despite it on the DISabled to ENabled podcast this week. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Keep up with Ardra:https://trippingonair.com/https://www.facebook.com/trippingonair/https://www.instagram.com/ms_trippingonair/https://twitter.com/tripping_onairhttps://youtu.be/wW7yXFp563A Join our tribe of ENabled warriors who fight back against chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled twitter @DISabletoenableGet your FREE 7 chronic illness hacks doctors never tell you here. Follow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comWIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts appGet the written out version of the episodes here: https://mmini.me/transcription
In this episode, we're celebrating 1 fantastic year of this podcast! Big thanks to everyone for listening. This podcast would not be here without you. Have a listen out for a special blooper episode next week. And remember Warriors, stay ENabled! Join our tribe of ENabled warriors who fight back against their symptoms!:Facebook / ENabled Warriors Insta: @ DISabledtoENabled twitter @DISabletoenableWant to tips for managing your symptoms? Check out our blog: www.DISabledtoENabled.com Join the VIP waitlist to get the ENabled Warrior Tracker before anyone else click here to join through Facebook Messenger: http://mmini.me/waitlistEnter to WIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts app
In this episode, you’ll learn Natalie's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Check out Natalie's links:Follow Natalie:www.zebraonabike.co.ukhttps://www.cyclinguk.org/cycle-magazine/great-rides-natalie-wilsons-5000-mile-coastal-ride-around-great-britainGet your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Join our tribe of ENabled warriors who fight back against chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledGet your FREE 7 chronic illness hacks doctors never tell you here. Follow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comWIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts app Get the written out version of the episodes here: https://mmini.me/transcription
In this episode, you’ll learn more about cycling 5000 miles for EDS UK as we carry on our chat with Natalie Wilson. Tune in to the last part of our interview where we find out about Natalie's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Follow Natalie:www.zebraonabike.co.ukhttps://www.cyclinguk.org/cycle-magazine/great-rides-natalie-wilsons-5000-mile-coastal-ride-around-great-britain Join our tribe of ENabled warriors who fight back against chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled twitter @DISabletoenableGet your FREE 7 chronic illness hacks doctors never tell you here. Follow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comWIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts app Get the written out version of the episodes here: https://mmini.me/transcription
In this COVID 19 Special episode, we chat with Lisa Sniderman about how she's coping with the pandemic and lockdown. Listen out for Lisa's episodes in the near future. And remember Warriors, stay ENabled! Follow Lisa:"Keep Shining" youtube video:https://youtu.be/4wYJcnCvhyoMy book:https://www.amazon.com/Light-Darkness-Lisa-Sniderman/dp/1681605570/My websites and social media sites:alightinthedarkness.infodoyoubelieveinmagic.infowhataredreamsmadeof.comisloveafairytale.comaoedemuse.comfacebook.com/aoedemusemusictwitter.com/aoedemuseyoutube.com/aoedemuseHow to Thrive Facebook group:https://www.facebook.com/groups/2521920814702414/Lights in the Darkness-Artists, Authors, Musicians Creating to Heal-Facebook Group:https://www.facebook.com/groups/433332727132078/ Join our tribe of ENabled warriors who fight back against their symptoms!:Facebook / ENabled Warriors Insta: @ DISabledtoENabled twitter @DISabletoenableWant to tips for managing your symptoms? Check out our blog: www.DISabledtoENabled.com Join the VIP waitlist to get the ENabled Warrior Tracker before anyone else click here to join through Facebook Messenger: http://mmini.me/waitlistEnter to WIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts appENabled warriors thank you for supporting our sponsors. Today's episode is sponsored by BeeKeeper's Naturals. Start building your natural first aid kit today. Use code WARRIOR for 10% off your order.Read the transcription of the episodes here: https://mmini.me/transcription
In this episode, we chat with Natalie Wilson about Ehler's Danlos Syndrome and cycling 5000 miles! Learn more about EDS and the amazing things she's done despite it on the DISabled to ENabled podcast this week. In this episode, you’ll learn more about Ehler's Danlos Syndrome as we chat with Natalie Wilson about her diagnosis. The highs and the lows. Symptoms to medication to things she’s found to help her condition. In the next episode find out about how she cycled 5000 miles round the coasts of the UK! Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Follow Natalie:www.zebraonabike.co.ukhttps://www.cyclinguk.org/cycle-magazine/great-rides-natalie-wilsons-5000-mile-coastal-ride-around-great-britain Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comGet your FREE 7 chronic illness hacks doctors never tell you here. WIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts appGet the written out version of the episodes here: https://mmini.me/transcription
In this episode, you’ll learn Matt's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Follow Matt:https://friedreichsataxianews.com/category/little-victories-a-column-by-matthew-lafleur/Facebook - Matthew Lafleur Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Join our tribe of ENabled warriors who fight back against chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledGet your FREE 7 chronic illness hacks doctors never tell you here. Follow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comWIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts app Get the written out version of the episodes here: https://mmini.me/transcription
In this episode, you’ll learn more about writing columns and working for Bio News as we carry on our chat with Matt Lafleur. Tune in to the last part of our interview where we find out about Matt's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Follow Matt:https://friedreichsataxianews.com/category/little-victories-a-column-by-matthew-lafleur/Facebook - Matthew Lafleur Join our tribe of ENabled warriors who fight back against chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled twitter @DISabletoenableGet your FREE 7 chronic illness hacks doctors never tell you here. Follow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comWIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts appGet the written out version of the episodes here: https://mmini.me/transcription
In this COVID 19 Special episode, we chat with Daniele Hargenradar about how she is coping with the pandemic and life in lockdown. Listen out for Daniele's episodes in the near future. And remember Warriors, stay ENabled! Follow Daniele:https://diabetesdominator.com/www.lovemcm.comhttps://www.facebook.com/diabetesdominator/https://twitter.com/diabetesDomin8rhttps://www.instagram.com/diabetesdominator/https://www.linkedin.com/in/danielehargenrader/ Join our tribe of ENabled warriors who fight back against their symptoms!:Facebook / ENabled Warriors Insta: @ DISabledtoENabled twitter @DISabletoenableWant to tips for managing your symptoms? Check out our blog: www.DISabledtoENabled.com Join the VIP waitlist to get the ENabled Warrior Tracker before anyone else click here to join through Facebook Messenger: http://mmini.me/waitlistEnter to WIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts app ENabled warriors thank you for supporting our sponsors. Today's episode is sponsored by BeeKeeper's Naturals. Start building your natural first aid kit today. Use code WARRIOR for 10% off your order. Read the transcription of the episodes here: https://mmini.me/transcription
In this episode, we chat with Matt Lafleur about Friedrich's Ataxia and writing for Bio News. Learn more about Friedrich's Ataxia and the amazing things he's done despite it on the DISabled to ENabled podcast this week. In this episode, you’ll learn more about Friedrich's Ataxia as we chat with Matt Lafleur about his diagnosis. The highs and the lows. Symptoms to medication to things she’s found to help his condition. In the next episode find out about how he's reached an age that doctors said wouldn't be possible, and started to write about his condition to help others. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Follow Matt:https://friedreichsataxianews.com/category/little-victories-a-column-by-matthew-lafleur/Facebook - Matthew Lafleur Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comGet your FREE 7 chronic illness hacks doctors never tell you here. WIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts appGet the written out version of the episodes here: https://mmini.me/transcription
In this episode, you’ll learn Lauren's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Connect with Lauren:uninvisiblepod.comhttps://www.instagram.com/uninvisiblepod/https://twitter.com/uninvisiblepodhttps://www.facebook.com/uninvisiblepod/Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Join our tribe of ENabled warriors who fight back against chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledGet your FREE 7 chronic illness hacks doctors never tell you here. Follow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comWIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts app Get the written out version of the episodes here: https://mmini.me/transcription
In this episode, you’ll learn more about starting a podcast for people with invisible illnesses as we carry on our chat with Lauren Freedman. Tune in to the last part of our interview where we find out about Lauren's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Connect with Lauren:uninvisiblepod.comhttps://www.instagram.com/uninvisiblepod/https://twitter.com/uninvisiblepodhttps://www.facebook.com/uninvisiblepod/ Join our tribe of ENabled warriors who fight back against chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled twitter @DISabletoenableGet your FREE 7 chronic illness hacks doctors never tell you here. Follow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comWIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts appGet the written out version of the episodes here: https://mmini.me/transcription
0:00Enabled warriors, welcome to another edition of the special Coronavirus0:04episodes. We are here today0:06with Natalie Wilson and her episode will be coming out really really soon. So Natalie is a fundraising gal. Natalie works for EDS UK and wanted to have a bit of a chat about how the Coronavirus is affecting charities and in particular support groups. So hey, hey, Natalie, how you doing today?0:24Yeah, very well. Thank you. Awesome. So0:27let's have a quick chat about how you think COVID is affecting the sort of face to face meetups that you would normally have had with EDS patients.0:38Yeah, definitely. So I mean, part of a big part of a charity and what we do is support you know, everyone in the local communities with Ehlers danlos Syndrome, and we have a network across the K and of volunteers that run kind of physical support group meetings and As well as working on the fundraising manager for charity, but as well as working for the charity, I've also always volunteered to run my local support groups. I did this a long time before I started working for charity. And so I've always run physical support groups, and quite Luckily, about six months ago, and because of the nature of the condition, and the charity started running a few online and it was very much meant to be kind of a trial, you know, try get everything working, yeah, see if they work and that, you know, only started at the beginning of this year. And, and obviously, you know, since kind of all of the lockdown and kind of social isolation, isolation of them COVID all of the physical support groups have had to stop and and, you know, over These a lot of people in our community, sometimes the only time they come out for houses is to come to the support group meetings, you know, it's a big thing for them. And, and luckily, we've managed to move a lot of our support group meetings online. And I and it's funny funny, we're talking about this today because I ran my first local one last night. And the charity has been doing a lot of kind of more national things. So we've been having things like puzzle clubs and book clubs. Again, we've got a session every week that anyone can come and chat about their anxieties. But yeah, so coffee. So a lot of areas are having things like coffee mornings and things like that. And so I had I have my first proper meeting, you know, last night and it was good. We've talked a lot about kind of worries. And and it's very much you know, Normal support group meeting would be to talk about the problems with your conditions and you know where you can get help. And does anyone have any advice for me doing this, this and this but last night, it was very much that mixed with kind of COVID anxieties, and I think it hit God Of course, it's hit everyone really hard. It's hit, you know, lots of communities but for people with Ehlers danlos Syndrome, you know, a lot of people are seeing physios regularly and they're having help with massage regularly and you know, any anything that they're kind of doing is very much often supported by other people helping them in daily life. And, you know, cleaners and carers although care is obviously still still very much helping and, and our chat last night, kind of moved on to how can people start doing things themselves. You know, and a lot of people are having online meetings though zoom calls is kind of what we've been using to charity with their local physio, and to help them with new exercises or what exercises they should be doing now. And a lot of people last night in my meeting, we're talking about kind of like, self massage and how they're kind of relieving the aches and pains their muscles, so it was, yeah, it was quite a different meeting. And, but it's, it was good, and it was nice. And it and there was actually people in my meeting last night that have never been able to come to a physical meeting. Yeah, aren't travelled or they can't drive or it's even though I do the I do the Thames Valley area
In this episode, you’ll learn more about Hashimoto's, sleep apnea and anxiety as we chat with Lauren Freedman about her diagnosis. The highs and the lows. Symptoms to medication to things she’s found to help her condition. In the next episode find out about how she set up her podcast, Uninvisible Pod. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Connect with Lauren:uninvisiblepod.comhttps://www.instagram.com/uninvisiblepod/https://twitter.com/uninvisiblepodhttps://www.facebook.com/uninvisiblepod/ Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comGet your FREE 7 chronic illness hacks doctors never tell you here. WIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts appGet the written out version of the episodes here: https://mmini.me/transcription
In this episode, you’ll learn Paul's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Join our tribe of ENabled warriors who fight back against chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledGet your FREE 7 chronic illness hacks doctors never tell you here. Follow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comWIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts appGet the written out version of the episodes here: https://mmini.me/transcription
In this episode, we chat with Paul Ace about his wife's (that's me!) diagnosis of Multiple sclerosis aged 22 and how that affected us both. Learn more about Multiple sclerosis and how we got through it on the DISabled to ENabled podcast this week. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Join our tribe of ENabled warriors who fight back against chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledGet your FREE 7 chronic illness hacks doctors never tell you here. Follow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comWIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts appGet the written out version of the episodes here: https://mmini.me/transcription
0:00 Enabled Warriors, we are here with Brad Dell to have a quick chat about the corona virus that's going on. It's taking-- well it has taken, let's say over the world right now. And everything's kind of working out and it's a little bit crazy. So let's find out how things are where Brad is in California. So how are you finding things right now, Brad?0:21 I'm, so far I've been pretty at peace, because I've been able to read a lot. And I've always wanted more time, sorry, ever. I'm trying to be more empathetic to the struggles of those around me. And when I do think about the things that are happening, I feel a lot of anxiety. I've been very privileged to be taken care of and to still have my job, but I know that many other people are suffering and that's very anxiety inducing to think about. Yeah,0:51 yeah, totally. And have you been doing doing things like limiting the news and kind of trying to do more meditation or anything like that? Have you kind of found any coping mechanisms.1:01 Yeah, so I have what I call a ritual list. And that list is basically kind of like a bullet journal where I mark off the things that I did each day. And so I have items like yoga or meditation or did I drink my three cups of coffee and, you know various things that helped me calm down. And so I'm strictly following that list and keeping focused on self care.1:27 I love that that's awesome. Well, what what are things like in California right now what they kind of advising and telling you to do and stuff?1:34 Yes, so... California was one of the first states in America to shelter in place where we have to stay locked down in our houses. And because of that, we have significantly flattened the curve. We are doing very well right now in comparison to the rest of the US and we have no idea when it will end but thankfully California because of the industries that we have, a lot of people are able to do remote work. So we better off than most states in the US and doing well. Yeah.2:04 Cool. That's pretty good. So, are they kind of all the states kind of competing against each other, like you can flatten the curve? and things like that.2:12 Yeah, America is naturally very competitive in itself. So states are all you know, who's doing better? Who's doing better?2:21 Okay, that's not a bad thing. If it can, you know,2:24 it's great in this case.2:26 And, uh, but um, well, it's not really changed for you as much. But you kind of work from home anyway.2:32 Yeah, yes, I already work at home. I usually I work in coffee shops. And I get a lot more exercise and so I'm trying to fix things and get a lot more exercise be more active. It's really showing when I tried to sleep at night and I have so much pent up energy. I can't even close my eyes.2:50 Oh, gosh. That is one thing that I'm missing is going to coffee shops and working in there because like, yeah, it gets a bit relentless, isn't it?2:58 Yes, yeah.3:00 I'm also really missing meals out this week. I don't know why this week in particular, but like every time I get to cook something I'm like, yeah. So yeah. So how do you think the COVID virus has really affected you up till now?3:15 So it's involves a lot of logistical changes. I normally stay in a house with three housemates and all of them are essential workers. And so that wasn't really going to work for me because I'm immunocompromised. So if they're going out more chance that they'll bring the virus soon. So thankfully, I have a very, very generous family at my church, and they have a very nice guest house that they've allowed me to stay in. Since I've been staying there, emotionally, I think kind of the biggest problem has been a lot of burden marrying a lot of people. They know that I've been through isolation, that for about eight months during my transplant journey, I was in what right now sheltering in place. So a lot of people are coming to me for help with their anxiety and everything. And happy to help. But there comes a point where you hav
In this episode, we chat with Paul Ace about his wife's (that's me!) diagnosis of Multiple sclerosis aged 22 and how that affected us both. Learn more about Multiple sclerosis and how we got through it on the DISabled to ENabled podcast this week. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Join our tribe of ENabled warriors who fight back against chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledGet your FREE 7 chronic illness hacks doctors never tell you here. Follow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comWIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts appGet the written out version of the episodes here: https://mmini.me/transcription
In this episode, you’ll learn Hanna's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Follow Hanna:https://hannaboethius.comwww.facebook.com/hannadiabetesexpertwww.instagram.com/hannadiabetesexpertwww.twitter.com/hannadiabexpertGet your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Join our tribe of ENabled warriors who fight back against chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledGet your FREE 7 chronic illness hacks doctors never tell you here. Follow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comWIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts appGet the written out version of the episodes here: https://mmini.me/transcription
In this episode, you’ll learn more about how she became a Diabetes Expert as we carry on our chat with Hanna. Tune in to the last part of our interview where we find out about Hanna's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Follow Hanna:Links for her episode:https://hannaboethius.comwww.facebook.com/hannadiabetesexpertwww.instagram.com/hannadiabetesexpertwww.twitter.com/hannadiabexpert Join our tribe of ENabled warriors who fight back against chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled twitter @DISabletoenableGet your FREE 7 chronic illness hacks doctors never tell you here. Follow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comWIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts appGet the written out version of the episodes here: https://mmini.me/transcription
0:00 Enabled warriors, we are back with Paul Ace, my lovely husband. We have a quick chat about COVID. So, Paul, you are with me in the UK right now? Yes. How do you think COVID has affected our way of life?0:16 Erm... I think the social aspects you don't realise like, I'm wish, like giving someone a hug. Oh, you know, like, you don't realise how much I actually seen someone in person is such a different relationship. Yeah. And from, you know, from a health perspective, my side I've just been really conscious about making sure I've stayed healthy so you can stay healthy.0:41 And yeah, my hands are pretty dry.0:46 I mean, we've, the first week that COVID came into the UK, I was watching the news every day and that's the first time watching us for a long time.0:55 You could tell as well, because you'll- my whole mind was just off everything. Yeah, you can't focus on anything. That was real.1:04 Exactly. So so as soon as I stopped doing that, I was like, Oh, well, this is better.1:10 Yeah, but the thing is the thing. I think the thing that we are kind of thinking about now is what's going to happen after this, you know, like, what's going to be a new normal because he can't go back to the way that it was? Well, I'm very curious as well.1:25 So it's highly contagious right now. When will it stop being highly contagious? Like the talking about herd mentality, but I'm not quite sure. Where that like whether that will make people more immune or not going forward? Will it be a lower strain going forward? Or is it just going to be as it is right now? Is this going to happen every year? No one knows yet?1:51 Well, no, I think until they come up with a cure and until1:56 then, I do1:57 think is the best time ever in history. To start an online business,2:01 yeah, you do bang on the base quite a lot. Yes, go with a good reason2:06 why and why, why, right- . Here's the thing. online businesses, recession proof. Like I can tell you with the clients that we've been working with, like they're all doing even better now. And what's the other thing? They don't not rely on? Anything else that goes wrong in the world? like they've got their own little bubble going on? Yeah. And if anything like it's growing, so just think, I think the biggest thing from COVID is it's just sped up the whole digital transformation of the world where what might have took another 10, 20, maybe 20 years, we've kind of done that in three months.2:49 We've had to, we've had to because again, it's about adaptive situations, and making the best of the situation.2:56 Yeah, and this note, got no choice. You just got to do what you've just got to do. Do what you've got to do and, and, you know, anyone who's being silly enough to do a social gathering right now, it's just idiotic.3:08 I don't know why anybody is doing that.3:11 You know, and it's really interesting to see how many people are now know what zoom is?3:18 Yes. Including your dad who is a complete technophobe.3:21 Yeah. Who ringing you up going? Well, how do we use zoom? Because I need to speak to so and so. In your meeting? How do we use zoom? How do I set up the call?3:31 It's amazing, which is great. And it shows how it can you know, write my mom's considered high risk? Yeah. So it means my dance having to do a lot more of the things like the shopping and everything like that. I mean, the3:43 first time ever,3:44 yeah. So you just have to learn. You have to learn different skills when you put on the pressure. And so, you know, environment wise as well. There's a lot of positives that have come out of that part in terms of seasonality. levels have gone down, which is good, obviously, that the deaths are not not good at all. I think the news is skewed a lot of that, to make it look like there's a lot of healthy people dying a lot of the time. It has sped up things where people have already got an underlying health condition. And if you've got an underlying health condition, avoid all contact with other people. Lik
In this episode, you’ll learn more about Diabetes and Hashimoto's as we chat with Hanna Boethius about her diagnosis. The highs and the lows. Symptoms to medication to things she’s found to help her condition. In the next episode find out about how she became a Diabetes Expert! Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Follow Hanna:https://hannaboethius.comwww.facebook.com/hannadiabetesexpertwww.instagram.com/hannadiabetesexpertwww.twitter.com/hannadiabexpert Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comGet your FREE 7 chronic illness hacks doctors never tell you here. WIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts appGet the written out version of the episodes here: https://mmini.me/transcription
In this episode, you’ll learn Sneha's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Follow Sneha:Instagram - @snehadave98Twitter - @snehadave98LinkdInhttps://www.usnews.com/topics/author/sneha-dave Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Join our tribe of ENabled warriors who fight back against chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledGet your FREE 7 chronic illness hacks doctors never tell you here. Follow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comWIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts appGet the written out version of the episodes here: https://mmini.me/transcription
In this episode, you’ll learn more about how she set up Health Advocacy Summit as we carry on our chat with Sneha Dave. Tune in to the last part of our interview where we find out about Sneha's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Follow Sneha:Instagram - @snehadave98Twitter - @snehadave98LinkdInhttps://www.usnews.com/topics/author/sneha-dave Sick of negative Facebook groups?Join the ENabled tribe:Search Facebook or click: ENabled Warriors Or search Insta: DISabledtoENabledJoin our tribe of ENabled warriors who fight back against chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled twitter @DISabletoenableGet your FREE 7 chronic illness hacks doctors never tell you here. Follow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comWIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts appGet the written out version of the episodes here: https://mmini.me/transcription
Enabled warriors Welcome to another Corona chat. This is a bonus episode that we're doing throughout the Coronavirus to help keep spirits up and find out what things are like in other parts of the world. So today we are chatting to Jameisha Prescod, and we're gonna have a chat about her lupus medication hydroxychloroquine that is potentially going to be used as the antidote to the Coronavirus. There's a lot of speculation in America right now and it's since come out that President Trump is taking this medication to 'ward off' the covid19 virus.
In this episode, you’ll learn more about Ulcerative Colitis as we chat with Sneha about her diagnosis. The highs and the lows. Symptoms to medication to things she’s found to help her condition. In the next episode find out about [COOL STUFF THEY’VE DONE. e.g. How they climbed a mountain, the business he started to help improve people affected by diabetes] Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Follow Sneha:Instagram - @snehadave98Twitter - @snehadave98LinkdInhttps://www.usnews.com/topics/author/sneha-dave Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comGet your FREE 7 chronic illness hacks doctors never tell you here. WIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts appGet the written out version of the episodes here: https://mmini.me/transcription
In this episode, you’ll learn Amin's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Connect with Amin:medangel.cohttps://www.facebook.com/MedAngelCO/https://twitter.com/MedAngelCOhttps://www.instagram.com/medangelco/rtGet your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Join our tribe of ENabled warriors who fight back against chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledGet your FREE 7 chronic illness hacks doctors never tell you here. Follow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comWIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts appGet the written out version of the episodes here: https://mmini.me/transcription
In this episode, you’ll learn more about how he founded MedAngel as we carry on our chat with Amin. Tune in to the last part of our interview where we find out about Amin's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Connect with Amin:medangel.cohttps://www.facebook.com/MedAngelCO/https://twitter.com/MedAngelCOhttps://www.instagram.com/medangelco/rt Join our tribe of ENabled warriors who fight back against chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled twitter @DISabletoenableGet your FREE 7 chronic illness hacks doctors never tell you here. Follow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comWIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts appGet the written out version of the episodes here: https://mmini.me/transcription
0:57 Okay, so in this episode of the special In a chat, kind of special episodes that we're doing here, we've got Audra, who is based in Canada, and we're gonna have a chat about the kind of, you know, weird things that are going on right now and hopefully provide some humour and a little bit of inspiration to make this a bit lighter. So how are you finding things right now?1:21 You know what, it's actually okay. I have not been out of my apartment in a month. So, um, but I think we're just I feel safe. We're doing what we have to do. We're saving lives. It's temporary. I mean, I think the world is not gonna be the same at the end of this, but it's managing. Well, I mean, listen, we have a roof over our heads. We have internet access, we have enough groceries. Everyone that I love and care about so far is safe and safe. I'm focused on that and just like doing what we need to do right now.2:05 Yeah, million percent Williamson. I mean, I read your blog the other day on how you're kind of finding things, and working from home with your partner.2:15 Just tell us a little bit about that. Yeah, I mean, I2:19 I already work from home and now I'm just reminding myself that this is our apartment and not like I do. I'm used to a lot of alone time but I mean, we live in a big city. So real estate is tricky, right? Like we have an open concept loft. So everything happens, basically in one room, right? Like it's like the cooking, the eating, the relaxing the working. And actually, I feel like both of us are working more than we normally would like, it's hard to just turn it off. I think we need to like figure out a way to be like, okay, it's five o'clock. Turn off your computer and figuring it out. How do we differentiate the days like my most recent suggestion was like, Martini Monday to Tuesday. Hey,3:16 you know what day it is? What are we drinking?3:21 is awesome. I love that. I love that and the thing that's really annoying is that whenever you like I send my husband to the supermarket now so I don't have to go. I just kind of see him. And he always says like, yeah, the hell gone. I was just empty so we couldn't really get anything. Oh.3:39 Um, so yeah, is it like that where you are like, um,3:42 yeah, so my husband actually went to do groceries this morning and waited for an hour in line in the parking lot to get in before but I we we kind of we stopped pelts and booze early on. So we're set.3:59 That is a good tip. Do we do the opposite sort of thing? We stop? We literally stockpiled easter eggs.4:06 We have a fridge. That's good.4:09 Nothing else4:11 about that. It's so funny.4:15 Oh god. So how does how's your partner finding working from home? Is that like, is that like for the first time for him? Do you think?4:25 I mean, he has taken the odd day from home. But it like for him consistently. It's tough. And he is used to being way more active. So he, he like he walks to work and I think that part he's missing but I think he's also he also kind of has this like can do spirit of we're just doing what we need to do. We'll get through it, you know. So I think the thing that's going to be tough for us, like bigger pictures and we travel a lot like every couple of months. somewhere. I really don't think we're going to be travelling probably for a year so that's going to be tough but we are getting a puppy. Oh wow. That feels like a pretty good consolation prize. So for sure and that will definitely keep you busy. Yeah.5:21 Can we get into a little bit more detail about the puppy?5:24 Puppy for cute so we actually we had a dog that we lost in December she's she's the best dog ever. Um, so we are dog people and we are like really feeling that loss especially right now. You know, it would just be so great to have a dog in your lap. So she's coming end of June.5:50 Can't5:53 it's like anybody out there follows me on instagram you will know I post a picture of my dog. The deck is6:00 She's just always doing something funny and cute. Yeah, t
In this episode, you’ll learn more about Diabetes as we chat with Amin Zayani about his diagnosis. The highs and the lows. Symptoms to medication to things she’s found to help his condition. In the next episode find out about how he developed a way to monitor the temperature of his insulin at all times. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Connect with Amin: medangel.coPlease provide your social media links:https://www.facebook.com/MedAngelCO/https://twitter.com/MedAngelCOhttps://www.instagram.com/medangelco/rtJoin our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comGet your FREE 7 chronic illness hacks doctors never tell you here. WIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts appGet the written out version of the episodes here: https://mmini.me/transcription
In this episode, you’ll learn David's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Connect with David Lyons:MS Fitness Challenge free online trainingMS fitness challenge facebook group Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Join our tribe of ENabled warriors who fight back against chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledGet your FREE 7 chronic illness hacks doctors never tell you here. Follow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comWIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts app Get the written out version of the episodes here: https://mmini.me/transcription
0:00 Enabled Warriors. We are here with Matt Lafleur. Just have a quick chat about how the coronavirus is kind of affecting everybody worldwide because it's kind of like a challenging and unique time to be alive I think right now, isn't it? And it's, it seems to be affecting us all really, really differently. So, hey, Matt, how you doing? Matt is here with us today. He is based in Louisiana. how things are there? I mean, what kind of things are happening in the US right now?0:29 in May in Louisiana in particular.0:33 It's been really slow moving to take the virus seriously. All right. Okay. really unfortunate.0:44 For a long time, people were, very dismissive.0:49 I tried to shelter at my place. Stay here most of the time. And that was a let down on my most other friends. Most people thought that I was making too big a deal, but1:05 turns out that it is a big deal.1:09 Yeah, I'm surprised that your friends are saying that1:12 now everyone is man.1:15 I'm not by myself.1:20 So slowly but surely everybody's seen a lot more seriously.1:25 Yeah.1:26 That's encouraging to see cuz I think that will be the key to getting over it. And getting beyond this when you take it seriously now.1:41 You know we can be free in the future.1:44 Yeah, exactly. So you kind of1:48 obviously you're staying inside a lot more now. What was the kind of scenario around where you are in terms of like our shops open and things like that or if they are closed now.2:00 They are open.2:04 They encourage the workers to stay home.2:07 Yeah, okay.2:10 So a lot of people are staying home but they're still able to go out and get2:17 groceries and get a2:20 food from my shops to go.2:24 But beyond that life is pretty much loaded.2:28 Yeah. It's really weird. It's a really weird time.2:34 So we've got like supermarkets and things are open and that's pretty much everything. We actually find out yesterday that our Prime Minister has the coronavirus, which kind of felt that was a little amusing to be honest, because you kind of like you don't know if you haven't took your own advice.2:50 You know, but if I saw that,2:53 yeah, it's amusing. And I think I mean, it's difficult as well to say Kind of whether he has took his own advice or not? Because obviously, you can kind of have symptoms for about 14 days, isn't it before you actually start showing symptoms? Um, so yeah, crazy. What do you think we'll kind of come out the other side of this? Do you think like how...? Yeah, what do you think will kind of come out of the other side of this? Do you think it'll promote more kind of accessibility in things like jobs and things like that?3:26 Um, in a strange way, I do see some positive things coming out of this. Because I think people are realising what really matters. The grocery store words, teachers, nurses, these are the people we're depending on right now. Yeah. And is encouraged to see that they're going to be seen as more vital in the grand scheme of things.3:56 Yeah, there's gonna be they're gonna have more respect for sure. I think4:01 I think that4:04 hopefully we'll be able to take our health more seriously. As we are here in the US, where4:13 healthcare is pretty much4:16 not enough for everyone4:19 think that we're saying that that it really should be. Hmm.4:24 Totally. Yeah. It's crazy, I think, because obviously, this is like, you know, it's it's tough and and people are losing people that they love and they care for and obviously, that's an awful thing. But I think in all of these sort of situations, I think it's so important to find some form of silver lining in it somewhere, you know.4:46 Yeah. And it's so easy not to,4:51 yeah.4:52 But your brightness, there is a silver lining, you know, at least it will be there. more compassionate to each other.5:02 Hmm, I think so. Definitely.5:06 At least one take hanging out with the general public not for granted.5:11 Yeah.5:13 I like the way as well that we - certainly my family - have been more. I'm kind of wanting
In this episode, you’ll learn more about Multiple Sclerosis as we chat with David Lyons about his diagnosis. The highs and the lows. Symptoms to medication to things she’s found to help his condition. In the next episode find out about [COOL STUFF THEY’VE DONE. e.g. How they climbed a mountain, the business he started to help improve people affected by diabetes] Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Connect with David Lyons:MS Fitness Challenge free online trainingMS fitness challenge facebook group Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comGet your FREE 7 chronic illness hacks doctors never tell you here. WIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts appGet the written out version of the episodes here: https://mmini.me/transcription
In this episode, you’ll learn Sally's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Connect with Sally on FacebookGet your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Join our tribe of ENabled warriors who fight back against chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledGet your FREE 7 chronic illness hacks doctors never tell you here. Follow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comWIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts app Get the written out version of the episodes here: https://mmini.me/transcription
In this episode, you’ll learn more about becoming a patient advocate as we carry on our chat with Sally Hatton. Tune in to the last part of our interview where we find out about Sally's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Connect with Sally on Facebook Join our tribe of ENabled warriors who fight back against chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled twitter @DISabletoenableGet your FREE 7 chronic illness hacks doctors never tell you here. Follow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comWIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts appGet the written out version of the episodes here: https://mmini.me/transcription
Catch Lauren's full podcast episode on the podcast soon! Go to: http://mmini.me/dtepodcast to subscribe right now so you can be notified. 1:25 So this is a1:27 crazy challenging kind of time and it's a time when none of us have really lived through anything like this. Have we is this really strange? With all this coronavirus and stuff and isolation? I kind of find the isolation thing quite amusing to help people the general Healthy People of the public I kind of handling isolation for the first time, in many ways. Yeah. And I think the chronic illness community are kind of a bit like1:56 this. This is kind of how it is all the time.1:59 Yeah. So anyway,2:00 we are here with Lauren Freedman and we can have a quick chat about Corona virus and how it's affecting her where she is. So whereabouts are you at the moment Lauren?2:09 I'm in my apartment in Venice in Los Angeles.2:12 Nice. And has the coronavirus affected you in any way do you think at the moment?2:18 I mean, most immediately, I have been practising social distancing and self isolation. So I've been in self isolation now for coming on two weeks, but we can have two weeks. I suspect we'll have to be practising social distancing and isolation quarantine for at least the next six to eight weeks if we have anything to go by based on what's happened in China and elsewhere in the world.2:50 And yeah, I'm loving it. I'm very much in my elements.2:56 I'm probably like the best and worst person to talk to about this because I'm an only child and I love being alone and I recharge with alone time. So being alone right now is like a gift. Total gift. It's so rare. I know some people are finding that it's a gift to be with their families. I'm like, it's a gift to not be.3:17 I know and it's3:18 so funny and it's, it's like I've been isolating for years. You know? I never really like hanging out with people. I work from home. So whenever we go out anyway, so kind of like, not a lot has really changed for us. And it's, yeah, it's really weird when I'd be out. anyone asked me this question, because I'm always going to write kind of the same, to be honest.3:40 Well, I think there are two there are two sides to this conversation like one is that this is second nature for those of us who are in the Sunni community. We know how to do this. No problem. We got this. The other is and I found this very interesting being a part of This community during this crisis, that so many employers are making work accessible right now to people out of necessity. And the number of people who are living with chronic conditions who have asked for accommodations in the past and been denied those accommodations, or in some situations denied that employment, because their lawyers were unwilling or unable to offer them accommodation, who are now watching people just being given accommodation, I think it's, it's lighting more of a fire under us. And making us a little bit resentful. You know, so that there's, there's the joy of knowing how to handle ourselves in solo sort of lockdown situations. There's also for a lot of people anxiety, and that comes along with that, which I can totally understand because it might remind us of relapse. It might also be might be The kind of people who get anxious when we sit still, you know, um, but then that resentment that's come out of watching able bodied people get everything they want, as per usual, and, you know, having lost opportunities because of the lack of access. And it makes it very clear to me that our understanding of work and life needs to completely be overhauled, that employers need to start offering accommodations across the board. And be doing that for people because of childcare. We doing it because of ability because of, you know, this makes it easier for my commute, whatever it is, why do you want people to sit in traffic for three hours just so they can be you know, and this is something that5:54 I didn't know.5:55 Yeah, it's ridiculous. Really. I know te
In this episode, you’ll learn more about XLH as we chat with Sally Hatton about her diagnosis. The highs and the lows. Symptoms to medication to things she’s found to help her condition. In the next episode find out about her XLH patient advocacy. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Connect with Sally on Facebook Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comGet your FREE 7 chronic illness hacks doctors never tell you here. WIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts appGet the written out version of the episodes here: https://mmini.me/transcription
In this episode, you’ll learn David's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Mans search for meaning - victor frankle Click here to get your copy: https://mmini.me/meaning Connect with David Francisco: www.DavidFranciscomusic.com Book and album are available spotify, apple music and all other good music platforms Social media search: @davidfranciscomusicGet your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Join our tribe of ENabled warriors who fight back against chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledGet your FREE 7 chronic illness hacks doctors never tell you here. Follow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comWIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts appGet the written out version of the episodes here: https://mmini.me/transcriptionThis episode is sponsored by our friends at Beekeepers Naturals. Check out their natural medicine cabinet full of all-natural medicines that bees make. Use code WARRIOR for 10% off.
In this episode, you’ll learn more about how David turned to music and started speaking about driving safety after his accident as we carry on our chat with David Francisco. Tune in to the last part of our interview where we find out about David's not-so-super-quick secrets. You’ll discover their favourite book, favourite place, scariest thing they’ve done and (our favourite) the weirdest thing they’ve ever done. What actions do they think needs to change to help people with chronic illnesses. Discover what is still possible after a diagnosis or accident, only on the DISabled to ENabled podcast. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Connect with David Francisco: www.DavidFranciscomusic.com Book and album are available spotify, apple music and all other good music platforms Social media search: @davidfranciscomusic Join our tribe of ENabled warriors who fight back against chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabled twitter @DISabletoenableGet your FREE 7 chronic illness hacks doctors never tell you here. Follow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comWIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts app Get the written out version of the episodes here: https://mmini.me/transcription
Warriors thanks for joining me for another episode of The disable to enable1:00 podcast with me Your host Jessie as today's episode is sponsored by our friends at beekeepers naturals natural health products created by bees. The products are so good that I have not had a cold the entire winter. Did you know that without bees we'd have no coffee crazy. Check out mi.me slash Bs and use code warrior Timpson off today or click the link in the show notes by clicking this link by the way beekeepers naturals will give back to the disabled to enable podcast. Hey, no worries. Okay, we are here with Hannah Marie theists to have a chat about how the coronavirus is affecting her at the moment. So So Hannah is based in Switzerland, and I'm in the UK. So let's have a chat about how each of our countries are kind of dealing with this whole pandemic. Whatever the calling it now epidemic pandemic, I have no idea. It's all a very scary kind of time. So let's have a chat with Hannah about how she is feeling about the whole Corona virus type thing and what2:00 She is doing to kind of keep yourself healthy. Hey, how's it going?2:07 Yeah, um, well, thank you. Thank you for asking. I know these are very troubled times for a lot of people and there's I think there's actually most mostly worry and anxiety around rather than actual illness. Yeah, sure, we're getting excited about the illness rather than the actual illness. Thankfully still, but2:27 I personally as we were talking about before, my routines haven't really changed.2:35 Switzerland yesterday got new directives on what we should do and what we can and can't do and sort of thing and what we've been asked to do. Although I'm not Swiss, I have been living here for over 20 years now. So I consider myself more Swiss than anything else. And and it's basically it went from sort of events can have 100 people and restaurant and bars can have 50 people and you know, don't3:00 overly interact with people and stay away if you're sick and wash your hands and all that all that normal stuff, but yesterday we got more directives and now it's really no restaurants are shut. All shops apart from grocery stores are shut yes stations are open medical care is open but basically everything else is everything social hairdressers are down and you know all small shops and I really, really actually feel very, very big heartache for all these people who are going to lose most or all of their income in business. For this time being a small business owner myself, thankfully everything for me is online, but for other people it's not.3:43 And I just hope that everyone gets to stay healthy and happy and, and calm and peaceful through this3:51 with the help of these directives and also, more over Switzerland also has basically close the borders. So that4:00 You can only get in if you're Swiss or if you're, if you have sort of a permit to live here.4:07 And both trains or public transport and, and flights and everything have been massively reduced, just to not keep people together. And it is, of course, a very, very serious situation. And I am glad that Switzerland is reacting in this way. Because then maybe we have a chance to actually flatten the curve. And I've been at home since Oh, about not even a week. But as we were saying before, my, my schedule hasn't really changed because I work from home and I sleep at home and I eat at home and in all these things. And in kind of visiting my businesses, I don't go out much during the week anyway. So it's not a huge thing for me to not have to stay home but be asked to stay home. And because of course5:00 chronic conditions people and especially immune, or new people are one of the risk groups.5:08 Yes, maybe a little bit more. So if you have a high blood sugar as a as in this specific case of diabetes, then if you have normal one, but still, we're part of the risk group. So I'm not really very sad5:21 at home right now and try to do my part, show solidarity with those who have
In this episode, you’ll learn more about spinal cord injury and life after an accident as we chat with David about her diagnosis. The highs and the lows. Symptoms to medication to things he’s found to help his condition. In the next episode find out about how he has spoken about driving safely and how he released an album. Get your ENabled Warrior Symptom Tracker book to help track and manage your symptoms, instantly spot triggers and get the best possible care from your doctors Connect with David Francisco: www.DavidFranciscomusic.com Book and album are available spotify, apple music and all other good music platforms Social media search: @davidfranciscomusic Join our tribe of ENabled warriors and fight back against your chronic illness!Facebook / ENabled Warriors Insta: @ DISabledtoENabledFollow our founder Jessie Ace as she shares her journey with Multiple Sclerosis and starting a business on www.jessieace.comGet your FREE 7 chronic illness hacks doctors never tell you here. WIN $100! Leave a review on iTunes, and each month we’ll choose one person at random to win. Here are some prompts to help you: who was your favorite guest and what did you learn from them? Will you listen to another episode? What did you like best about the show? Click here to learn how to leave a review on desktop and on a Phone. Android users may need to download the apple podcasts app Get the written out version of the episodes here: https://mmini.me/transcription
Part 3 Mrs Dalaway - viginia woolf a celebration of life. Reminder of how much you can do in a day. Weirdest thing: played competitive table tennis, dressed up as her dog, dog and owner look alike competition, Amazing place - Sweden. Roadtrip with mum and two brothers the year her dad died. Flew to Gothenburg to Stockholm. Scariest thing - voluntarily going on a banana boat. Scarier things that were not so voluntary. Connect with Celestine:www.glowwormfilms.co.ukTwitter - @celestinefraserInstagram - @celobean Sick of negative Facebook groups?Join the ENabled tribe:Search Facebook: ENabled Warriors Or Insta: DISabledtoENabled Reduce stress now go to ENabledwarriors.org our free Facebook messenger 5 day stress course ______________________ This episode is sponsored by our friends at Beekeepers Naturals. Check out their natural medicine cabinet full of all-natural medicines that bees make. Use code WARRIOR for 10% off.
Part 2 We discuss gratefulness. CFS had so much stigma, you get people saying ‘i’m tired too I had a late one last night’. When you tell people you have a genetic condition of EDS and PoTS they treat you differently. It meant I had better care and treatment from doctors because people took it more seriously. It took Celestine. I’m not I’ve ever come to terms with it, it’s something I’ll always be coming to terms with. As a child, you never think you’ll get any kind of diagnosis. It feels so good to have answers. I produced a short documentary, ill, actually. It follows 3 young people with difficult chronic illnesses and how they each navigate social media. Some are open about itt online and build communities around it and others don’t talk about it at all and others wouldn’t even know there was something wrong. We got funding and It all happened very very quickly, it was an intense process. We’d worked on it for about 3 years. Working out what story we wanted to tell. Zoe Hunter-Gordon the director worked on it together. Learning about the research needed to be done. Reaching out to different charities. BRI/BBC scheme celebrating the anniversary of the internet. Aout embracing the digital. Got on to the born-digital scheme. How each of the people used social media to show their illness in very different ways. Ben - @benmudge_Jameisha - @youlookokaytome/ They’ve all found ways to make a career alongside their conditions. Celestine couldn’t find any representation in films/tv that focused on young people with disabilities. It was born from an absence of representation. Is disability becoming a more socially recognizable thing? People relate to disability in a very obvious way, i.e. A Wheelchair. In programs, they use wheelchairs as a dramatic plot twist. The stores don’t have to be disabled storylines but wouldn’t it be nice if invisible disabilities were included in storylines? Celestine set up her own production company Glow worm films so look out for that! She wants to focus on the people who don't have much representation. There are a lot of minorities that need representation too. Would you prefer to have an illness that’s invisible or visible and why? Let us know in the comments. ‘Elderly people ask me to get up for them on the tube’ Hear Celestines advice for people newly diagnosed. Connect with Celestine:www.glowwormfilms.co.ukTwitter - @celestinefraserInstagram - @celobean Sick of negative Facebook groups?Join the ENabled tribe:Search Facebook: ENabled Warriors Or Insta: DISabledtoENabled Go to www.DISabledtoENabled.com for help and advice on how you can live well with a chronic illness Reduce stress now go to ENabledwarriors.org our free Facebook messenger 5-day stress course______________________ This episode is sponsored by our friends at Beekeepers Naturals. Check out their natural medicine cabinet full of all-natural medicines that bees make. Use code WARRIOR for 10% off.
we are here with Sneha Davi let's have a little bit of a chat about the coronavirus because Coronavirus or COVID-19 is something that is affecting everybody right now. It is a global worldwide thing.And for people with chronic illnesses it is you know, obviously a really worrying time for everybody, though, so say how whereabouts are you at the moment and how is it kind of affecting you? Yeah, so um, so I am alsoclassified as an immunocompromised individual. And so I think, you know, initially, it had been incredibly terrifying for me. And it still is because, you know, the more you hear about it, and the more you hear stories, it becomes even more anxiety-inducing, at least for me. And so I think, you know, the biggest thing, it's affecting every part of my life right now, as I'm sure it is for everyone around the world. But you know, for me, specifically, my university is now going to be entirely online, which is bizarre to me, because last year, we, you know, struggled to even cancel one day of school because of a snow day. And I go to a large public university, and so it brings in an additional challenging dimension. And so I think another thing is, too is that I currently cannot go home to my parents as well because my dad is a provider and he has seen coronavirus patients so for fear that he is a carrier because of the reallyEasy to catch it is really, he does not want you to same location as he is. And so it's been kind of tricky to because I'm kind of stuck where no one is at my college, you know, college town. And that's been interesting as well. And and the other thing too is that I am in between infusions in starting different infusions. And so I really need to get on another infusion because my previous one causing allergic reaction and, but I'm just having to kind of wait this out because that will make me even more immunosuppressed and taking that's also been interesting, and I quite frankly don't even want to go inside a hospital right now. Um, because of the fear of COVID patients there as well. So I think it's been hard and also just my day to day things that I do like climbing, going to coffee shops and everything like that has been, it's just been kind of hard to be in my house, even though I have you know, went through a period of about five years of, of real isolation. This isThis kind of hits differently because right now I'm able to, you know, like, go outside and climb and stuff like that. Whereas earlier, I was really sick and I didn't feel like going anywhere. So isolation was a little bit easier at that time. Yeah, definitely. And I think, um, and it's the same for you, but I kind of feel like, it's not just the virus. That's scary, but I kind of feel like, I'm kind of scared of the public reaction to it. Yeah, in the UK, we've had lots of like, things like stockpiling and things like that CES, as you saw, you know, getting emptier and emptier and things likethat. they've, they've kind of been a little bit. And I don't know if this is right or not, maybe, maybe, but I kind of feel like they've been quite reactive in the government's approach to the coronavirus in the UK. I mean, it was only yesterday. Our schools are still open. And, wow, why? Things to select None for now, but they made a decision yesterday to put something in place called social distance.You've heard about this. Oh, absolutely. Oh, yes. Yesterday a meter over away from everybody right now, apparently.So we've got to stay away from everybody say, Yeah, like a meter away from everybody. And then they've closed bars and restaurantsand theatres and stuff like that. So, yeah, people are really kind of self-isolating at home now and right. It's a weird time to be alive. It'sreally, it's really bizarre even my professors during my last class, because at that time, we, we had only had two weeks of virtualclasses. But as of a couple of days ago, the rest of the semester is virtual classes, but even our professors were like, kind of like it
Topics discussed: What is Ehlers danlos syndrome (EDS) and post tachycardia syndrome (P.O.T.S)?Ehlers danlos syndrome is a group of connective tissue disorders. Celestine has hypermobile ehler’s danlos syndrome. EDS is A deficiency of collagen - a protein - it’s the glue that holds your body together. Affects her joints by partial dislocations and causes chronic fatigue. puts a lot of pressure on the joints because the muscles aren't’ strong enough to hold them. P.o.t.s - is a dysfunction of the autonomic nervous syndrome. Body temperature, heart rate, digestion, blood being circulated around. Both multisystemic conditions. People go through good and bad patches. It’s not a progressive illness, it's a collagen deficiency from birth. “You’ve got a slightly wonky body that wasn’t built right.” First signs, at age 17, noticed getting more tired than peers. Just after starting to drive, being taken to Abbey road by her driving instructor, Started having a terrible pain in her neck, thought she was anxious because of driving lessons. The pain got more and more intense. Lessons got shorter. She tried to just get on with A levels, but was getting more and more tired. She now thinks, ‘Maybe I should have intervened faster than I did’. Had a stressful time at home because her dad had been diagnosed with a type 4 brain tumour. He had to have major brain surgery. They all plodded on as best they could while he was going through treatment. This period of massive stress was when my symptoms started setting in. Stress is a major trigger with many people with P.o.T.S. Your body is in a flight or fight state constantly especially when your family is going through a really hard time. Celestine was in denial at first, worried people would think she had an anxiety problem and worried doctors would dismiss physical symptoms and put it down to anxiety. She was misdiagnosed with CFS, something a lot of young people particularly young women get diagnosed with. Most people diagnosed with that aren’t happy with the diagnosis because it’s more a diagnosis of the symptoms not the condition itself. She had symptoms that were different. Then she was dx with Myasthenia gravis - she couldn’t tell you a single thing about it now but at one time she was an expert. Celestine was put on a lot of steroids which made her self conscious as it affected her appearance. Then she went back to CFS and got really bad headaches. Saw a neurologist who was a headache specialist. He noticed she had a lot of markers for Hypomobility. He sent her to a rheumatologist. It was a big relief at the time. The diagnosis process is currently far too long at the moment. It needs to be sped up because people are becoming far sicker than they need to be and a lot of it is preventable. Hypermobile EDS doesn’t require expensive tests, it just needs a doctor to look at you and do the baker scale, hypomobility scale. Involves bending your body in a few different ways. It’s something GP’s could do it doesn’t require an expert. Never shared an illness story before because she felt she wasn’t taken very seriously by doctors because of age. Felt at times patronized by doctors and was diagnosed with anxiety in the first year of being ill. She says she doesn't think an 18-year-old girl is taken very seriously by doctors. You get told your body's changing anyway so new symptoms are just part of the deal. Connect with Celestine:www.glowwormfilms.co.ukTwitter - @celestinefraserInstagram - @celobean Sick of negative Facebook groups?Join the ENabled tribe:Search Facebook: ENabled Warriors Or Insta: DISabledtoENabledGo to www.DISabledtoENabled.com for help and advice on how you can live well with a chronic illnessReduce stress now go to ENabledwarriors.org our free Facebook messenger 5-day stress course______________________ Thank you to our friends at Beekeepers Naturals for sponsoring this episode. Check out their natural medicine cabinet full of all-natural medicines that bees make.
Part 3: My advice and super quick secrets round. The 5 stages of grief. Everyone goes through it. Nitika’s best piece of advice is going to a therapist who gave her permission to feel sadness and trauma that affected her body. Don’t think you have to take any advice from any non-medical people. ‘I have a team that I'm working with so thanks but no thanks.’ Connect with Nitika: https://nitikachopra.com/ Sick of negative Facebook groups?Join the ENabled tribe:Search Facebook: ENabled Warriors Or Insta: DISabledtoENabled Go to www.DISabledtoENabled.com for help and advice on how you can live well with a chronic illness Join the VIP waitlist to get the ENabled warrior Tracker Journal before anyone else click here to join through Facebook Messenger: http://mmini.me/waitlist________________________Thank you to our friends at Beekeepers Naturals for sponsoring this episode. Check out their natural medicine cabinet full of all-natural medicines that bees make. Use code WARRIOR for 10% off.
Part 2: Finding acceptance Nitika describes going through phases of acceptance and phases of feeling low. Hitting rock bottom at 25 was tough but there was a level acceptance of ‘this is where I’m at’ I just have to figure this out and deal with it.’ Setting up something bigger than herself to help others. She set up Bella Life Magazine and had 100 people writing for the magazine, and started posting YouTube videos and online. She was soon approached by the exec of a production company and offered her her own talk show - naturally beautiful. ‘I’ve officially done everything I could have to get me to this place.’ Nitika also discusses how she started running events and inspired by going to an event called, ‘curvy con’, she decided to set up a convention for chronic illness. Connect with Nitika: https://nitikachopra.com/ Sick of negative Facebook groups?Join the ENabled tribe, all chronic illnesses welcome. Search Facebook: ENabled Warriors Or Insta: DISabledtoENabled Go to www.DISabledtoENabled.com for help and advice on how you can live well with a chronic illnessManage stress now for free go to ENabledwarriors.org Facebook messenger 5-day stress course.________________________Thank you to our friends at Beekeepers Naturals for sponsoring this episode. Check out their natural medicine cabinet full of all-natural medicines that bees make. Use code WARRIOR for 10% off.
Part 1: The diagnosis We discussed how she got her psoriasis diagnosis aged just 10 years old. As you can imagine growing up with psoriasis would have been pretty hard going. Kids are often blunt and unaware of feelings that Nitika said were a little bruised going through school. We talk about how she was ‘batting her body’ even from such a young age. Accepting her skin as it was and her curves were tough for a young kid. She describes how a kid should be carefree and enjoying the moment but things were especially hard for Nitika. She didn’t learn the best way in the linear way of learning at school. We discuss the commonalities of misdiagnosis in children. One thing Nitika found especially difficult when the middle of summer came around and had to wear long sleeves on the soccer field. Once it started it took over. Psoriatic arthritis caused Nitika so much pain at the age of 19. She was living at college as her parents moved back to India so she felt truly alone. Her mum was really against her taking steroids at such a young age. Medication was a mystery. She got better by around 60% and then stopped within roughly 6 months. That then triggered psoriatic arthritis. She couldn’t move, she couldn’t get out of bed to go to class. At 19 years old. Struggling to get out of her apartment to get to rehearsals meant missing out on experiences she had previously enjoyed. After getting married everything changed with her health. Coming to terms with the mindset was difficult leading to a divorce aged 24. Struggling to even keep doing a job, her parents living out of the country. About to give up… Something changed. Find out what in part 2. Sick of negative Facebook groups?Join the ENabled tribe:Search Facebook: ENabled Warriors Or Insta: DISabledtoENabled Reduce stress now go to ENabledwarriors.org our free Facebook messenger 5-day stress course.________________________Thank you to our friends at Beekeepers Naturals for sponsoring this episode. Check out their natural medicine cabinet full of all-natural medicines that bees make. Use code WARRIOR for 10% off.
Part 3 - Super quick secrets. We discuss Megan’s answer to the super quick secrets round. Hear about her crazy experience with acupuncture. Does acupuncture work for you? Let us know in the comments. Listen to Megan’s favorite place, have you been there too? I have always wanted to go to this place! We still can’t get over what Megan’s scariest thing was… shudders. Link to Megan:@meggfinch/Megg.Finch Sick of negative Facebook groups?Join the ENabled tribe:Search Facebook: ENabled Warriors Or Insta: DISabledtoENabled Reduce stress now go to ENabledwarriors.org our free Facebook messenger 5-day stress course.
Part 2 - Part 2 of our 3 part interview describes how she turned her diagnosis around and shows what is possible despite a diagnosis. Megan turned to cake baking to relieve the stress of her diagnosis. Megan is getting married! We discuss wedding planning with chronic illness. Stressors you come across and situations you need to be prepared for. Megan’s top tip for planning a wedding is to be super organised early on so that you can relax and enjoy the countdown to the big day. Don’t do your own hair and makeup - save energy!Delegate tasks on the day to our bridesmaids/mum/dad/dad’s girl friends, = less things for you to stress about. Plan on doing the least amount possible. Wedding fair tip: address labels for all the forms, Create a new email address specific for wedding How to avoid sensory overload Link to Megan:@meggfinch/Megg.Finch Sick of negative Facebook groups?Join the ENabled tribe:Search Facebook: ENabled Warriors Or Insta: DISabledtoENabled Reduce stress now go to ENabledwarriors.org our free Facebook messenger 5 day stress course.
Part 1 - Part 1 of our 3 part interview focuses on Megan’s initial diagnosis. Firstly, she was diagnosed with NMO (Neuromyelitis optica) then later diagnosed with MS. Megan tells us what it was like when she randomly went blind in one eye one day. She was put on a lot of steroids which she didn’t like. Megan tells all about the things that helped her such as a TENS machine and oxygen therapy with her local MS therapy center. Listen to how her diagnosis also created an unlikely relationship. ‘Steroids really affect mood, so that didn’t help’ Link to Megan:@meggfinch/Megg.Finch Sick of negative Facebook groups?Join the ENabled tribe:Search Facebook: ENabled Warriors Or Insta: DISabledtoENabled Reduce stress now go to ENabledwarriors.org our free Facebook messenger 5-day stress course. This episode is sponsored by iHerb for all the great brand supplements you could ever need at an affordable price.
Part 3 - check out these super quick secrets… Wow! We also discuss the Youtube show ‘Hot ones’ where celebrities have to eat the spiciest hot sauce whilst answering interview questions… Wonder if we should do that on the podcast?! Haha! Chris’ restaurant likes to say they give the middle finger to fine dining. We hear all about the science of food and how Chris incorporates chemistry into food preparation. Connect with Chris: https://twitter.com/holland_chefEat at his restaurant: https://www.dvinebar.com/ Sick of negative Facebook groups?Join the ENabled tribe:Search Facebook: ENabled Warriors Or Insta: DISabledtoENabled Reduce stress now go to ENabledwarriors.org our free Facebook messenger 5-day stress course. This episode is sponsored by iHerb for all the great brand supplements you could ever need at an affordable price.
Part 2: I have a moment where I'm like, ‘I don’t know how I'm gonna get through tonight’ but then the adrenaline kicks in and I’m fine I can get through it. The first time I was on the show was probably the best moment of my life (obviously after my son was born). Chopped was my favorite cooking show. Being on there was like being on a dream. I was standing 2 feet away from my idol and I was about to cook him dinner--it was insane. The judges were a lot nicer than they are on tv! Connect with Chris: https://twitter.com/holland_chefEat at his restaurant: https://www.dvinebar.com/ Sick of negative Facebook groups?Join the ENabled tribe:Search Facebook: ENabled Warriors Or Insta: DISabledtoENabled Reduce stress now go to ENabledwarriors.org our free Facebook messenger 5 day stress course. This episode is sponsored by iHerb for all the great brand supplements you could ever need at an affordable price.
Topics discussed: Initial diagnosis. Chris’s healthcare practitioners didn’t know what it was to start off with. The only thing he knew about MS was about wheelchairs, going blind and becoming a ‘cripple’. Chris didn’t handle his diagnosis well and originally was ‘playing up the pain’ so that he could get more drugs. He turned to substances so as to not deal with the MS. He spoke about it to get sympathy for it. For about 5 years he pretended he didn’t have an illness and just didn’t accept it. He says that once you accept there is nothing you can do about it, then you’re left with a decision between this disruptive behavior being your life and throwing it away or you can rebuild your life and start again. Are you a twin with a chronic illness? Interested to hear if one of you does and one of you doesn’t. Let us know in the comments. Connect with Chris: https://twitter.com/holland_chefEat at his restaurant: https://www.dvinebar.com/ Sick of negative Facebook groups?Join the ENabled tribe:Search Facebook: ENabled Warriors Or Insta: EnabledWarriors Reduce stress now go to ENabledwarriors.org our free Facebook messenger 5 day stress course.This episode is sponsored by iHerb for all the great brand supplements you could ever need at an affordable price.
Part 3 - super quick secrets round George’s inspiring book may surprise you! Weirdest thing? Apparently it may offend people… I felt sick. Most favorite place… Would you consider his answer to your favorite place? I’m not sure I would for the first part! Scariest thing… I did not expect George to say THIS. Connect with George: www.shift.ms Twitter: @GpepsSick of negative Facebook groups?Join the ENabled tribe:Search Facebook: ENabled Warriors Or Insta: EnabledWarriors Reduce stress now go to ENabledwarriors.org our free Facebook messenger 5-day stress course. ______________________________________This episode is sponsored by iHerb. Quality supplements at an affordable price for every need and condition, including pet healthcare. iHerb believes in providing an education to impoverished children worldwide will be the most meaningful, long-term return on investment. Go to: http://mmini.me/iherb this is an affiliate link, meaning for every purchase made iHerb supports the running of the disabled to enabled podcast. Please go get your supplements :)
Part 2: (includes mild language) After my experience of being diagnosed, I wanted to help others my age who were in the same position. I realised quickly that the people I was with that were in the clinic didn’t relate to me, I needed to find people younger than me. I was in my early 20’s desperately trying to figure out what this diagnosis meant for me. I found that challenging. Over time I found others in a similar situation and we shared ideas and feelings around diagnosis - realizing they were similar. When you have an online platform you have the opportunity to connect people from all over, when you get rid of the geographical barrier you could connect to anybody. George’s friends from university helped him shape how shift.ms is today. Being a charity was never the goal. The goal was to fill a gap in support for people diagnosed. Existing services weren’t meeting the needs of these people. Being proactive in the management of your MS is key. How to set up a charityIt was never the intention for it to be anyone’s job. The weird thing about setting up a charity and how a founder needs to employ their bosses. Setting up shift.ms helped George to come to terms with his own illness. We discuss Post Traumatic Growth in response to a diagnosis, a surprisingly common response. People who go through trauma want something good to happen as a result. Being diagnosed with anything is a traumatic experience. What happened when George approached major charities to pitch his ideas. We discuss shift.ms’s motto: we believe that MS doesn’t mean giving up on ambitions, just rethinking how to achieve them.Listen out for George’s top advice for newly diagnosedConnect with George: www.shift.ms Twitter: @Gpeps Sick of negative Facebook groups?Join the ENabled tribe:Search Facebook: ENabled Warriors Or Insta: EnabledWarriors Reduce stress now go to ENabledwarriors.org our free Facebook messenger 5 day stress course. ______________________________________This episode is sponsored by iHerb. Quality supplements at an affordable price for every need and condition, including pet healthcare. iHerb believes in providing an education to impoverished children worldwide will be the most meaningful, long-term return on investment. Go to: http://mmini.me/iherb this is an affiliate link, meaning for every purchase made iHerb supports the running of the disabled to enabled podcast. Please go get your supplements :)
Part 1 - Diagnosis (includes mild language) Diagnosed at 22. He started having pain in his shoulder, doctors thought it was a trapped nerve. Dismissed with ibuprofenAbout a month after, whilst at work, George could barely see. His balance was not right. Started continuously vomiting.Feared meningitis which was quickly ruled out by a lumbar puncture.Feared brain tumor, ruled out after scans. Quickly deteriorated. The hospital he was in at the time didn’t have an MRI scanner so another appointment was scheduledFound out he had MS which he hadn’t heard of. Automatically associated older people and wheelchairs. Diagnosis of MS is most common in their 20s-30s It’s a lifelong condition and there are far more treatments available now. George was put onto Rebif to start with then mitoxantrone, then Copaxone. Listen out for the daily checks George used to do (I used to do this too!) How to know the difference between a relapse and just a bad day. How George recovered from relapses. The false hope George was given by his neurologist.There’s no benefit in saying that things are going to be ok by a doctor. MS can be a cruel condition. It needs to be made clear that each individual has a level of responsibility for how their condition might turn out. There’s a huge support for changes in lifestyle and the role it plays in a long term health condition. That word ‘lifelong’ is scary but the thing I find most challenging to accept is the uncertainty. It can change at any time. ______________________________________This episode is sponsored by iHerb. Quality supplements at an affordable price for every need and condition, including pet healthcare. iHerb believes in providing an education to impoverished children worldwide will be the most meaningful, long-term return on investment. Go to: http://mmini.me/iherb this is an affiliate link, meaning for every purchase made iHerb supports the running of the disabled to enabled podcast. Please go get your supplements :)
Topics discussed: What happened when Shelby was diagnosed may shock you. From working as a makeup artist in TV and movies to relying on a service dog and teaching others the importance of service dogs. People tend to pay attention when you’re dying. Doctors not doing the right testsThe medical industry needs to get with the times because things are so different now. Eating is a challenge because of gastroparesis. I get a lot of back pain that a 28-year-old shouldn’t have. POTS and dystonia are heavy which makes showering really hard. I have low blood sugar problems which means I get really low levels when I go to bed which can lead to seizures.How do you train a service dog?BONUS Catch Shelby’s dog Luna in the background of the video on YouTube (search disabled to enabled) she is adorable. How to handle the general public when they approach your service dog and Tips for the general public on how to respond to a service dog. Did you know? A dog can smell the slightest hint of a chemical in the equivalent of 3 Olympic sized swimming pools? Check out https://www.starfleetservicedogs.org/ Shelby’s best advice for others diagnosed with a chronic illness. Links to connect with Shelby:insta.com/Service.angel.luna twitter.com/shelbyssmiles Find out more about She;by’s conditions: primary immunodeficiency, P.O.T.S, anaphylaxis, gastroparesis, mass cell activation syndrome (MCAS), dysautonomia, Ehlers-Danlos Syndromes EDS, Hypoglycemia, Medical professionals are told: When you hear hoofprints look for horses, not zebras. Meaning, if you think somethings wrong don’t think it’s anything too serious.______________________This episode is sponsored by our friends at Beekeepers Naturals. Check out their natural medicine cabinet full of all-natural medicines that bees make. Use code WARRIOR for 10% off.
We discuss the 7 pillars that make up the OMS (overcoming multiple sclerosis) program. Major benefits of eating healthily to help improve your overall health condition. The science behind the diet. The overcoming MS book (available for free to the major countries) The benefits of meditation, living in the present, managing stress and reducing anxiety. Overcoming MS encourages taking medication alongside a healthy diet, exercise, omega 3, vitamin D. We talk about Geoff taking Lemtrada. Differences in access to medicine around the world Exercise and chronic illness. Neuroplasticity in the brain. Does temperature affect your symptoms? If heat affects you, try a WrapMeCool (www.WrapMeCool.com) an instant cooling that looks like a normal scarf. Use code EW19 to get 10% off Super quick secrets! Listen out for: Sleeping on a volcano. Sorry, what?! And being chased by an orangutan. Standard. Connect with Geoff Allix:Overcoming MS podcastInstagramTwitter Sick of negative Facebook groups?Join the ENabled tribe:Search Facebook: ENabled Warriors Or Insta: EnabledWarriorsLearn to manage your stress now for free go to ENabledwarriors.org for our free Facebook messenger 5-day stress challenge. Click to open in Facebook messenger and click get started to begin. _________________________________________This episode is sponsored by Beekeepers Naturals. Since taking their bee propolis throat spray every day since the start of winter and I have remained cold-free! Check out the live video I did about it in the ENabled warriors group
Joanna stops by to discuss everything going on with her MS diagnosis. What started with waking up blind in one eye came as a complete shock to her - as it would to any of us. After numerous trips to the opticians, Dr's and neurologists and a couple of misdiagnosis’ in the end, it was found that she had MS. She didn’t dare tell her optometrist about the tingling in her legs when asked though, as she didn’t know what help it would be. Invisible symptoms and stuff people say. Would you prefer it if people just asked you questions? Did you use an online network when you were diagnosed? Joanna tells us of her experiences of using one called ‘MS Buddy’. There are also shift.ms and My MS Team which are fabulous for connecting with people also. Are there other ‘buddy networks’ for different chronic illness charities? If so comment below so we can share them for others. We also discuss setting up your own Facebook Group and how most Facebook groups are quite negative :( do you think we need to change the narrative of these or should they stay areas to vent online? Joanna talks about the MS therapy centre that she goes to and wants to encourage young people to go to also. But if you’ve never been to an MS therapy centre, are you likely to go? There is a danger for people with chronic illness to put things down to one condition or another but sometimes a weird symptom may not actually be your chronic illness at all and sometimes you should really go to your doctor. Joanna tells us how she could have been diagnosed so much sooner than 10 years if she got her initial symptoms checked out. How did your work organisation handle your illness? Did you tell them? Do you know what your rights are? We also discuss Reiki after Joanna’s newly qualified Reiki practitioner qualification. Have you heard of Reiki before? I’ll be honest, I hadn’t! We talk about the worst part of having an invisible illness. Joanna says for her the worst part about it is that it’s invisible in the first place! Also, people don’t understand how your condition fluctuates day to day. Do you find that? Joanna’s inspiring book recommendation is: #ad Rebecca Campbell: Light is the new black click to get it from Amazon. Like alternative, holistic therapies? Try reading Reiki For Life: The complete guide to reiki practice for levels 1, 2 & 3 Buy purchasing through the links on this page a small amount of money will go towards running of the disabled to enabled podcast and helping more people like you with chronic illness. Check out Joanna’s links below and make sure to check out the Wigan MS therapy centre. Connect: Twitter: @gimmehopejoannaInstagram: @gimmehopejoanna Sick of negative Facebook groups?Join the ENabled tribe:Search Facebook: ENabled Warriors Or Insta: @Disabledtoenabled Reduce stress now go to www.ENabledwarriors.org for our free Facebook messenger 5-day stress course. Click to open in messenger and then click get started to begin. ____________________________________________________Have you ever felt out of your depth in the kitchen? Do you keep cooking the same thing?Liven up your dinner tonight with Gousto and have meals like this... Get 60% off your first box and 30% off your first month (UK only) by clicking here: https://mmini.me/gousto
A slightly different kind of guest today. This guest doesn’t have a chronic illness but inadvertently created the most amazing mobility bike for people with chronic illnesses. DISCLAIMER Please be aware there is a lot of swearing in this episode. The opinions expressed in this episode are not those of DISabled to ENabled and are intended to spark discussion about issues relating to chronic invisible illness. Topics discussed?Mobility devices are designed to be a medical mobility aid that creates a social divide between people with and without a disability. The Alinker brides the gap between people with disabilities and without. BE set out to make something really cool so that people would be proud to use it rather than feel embarrassed. What is an Alinker? A cool mobility aid for active people who want to stay active despite mobility challenges. It’s bright yellow and looks a bit like a racing mobile. It helps people gain mobility back in their lives. It means that people are seen on a cool bike at eye level and you can be approached by able people without judgment. It means that we can challenge people’s assumptions. Who is the Alinker for? The Alinker is for everyone who identifies as an active person and who wants to stay active. It’s also for misfits and rebels. Gender identity.Why is the Alinker not considered a medical device? There is a very good reason. Should we rename the healthcare system to the ‘sick care system’? You’re then not focussing on the problem anymore. The problems facing our healthcare system. Climate changeHow can we be improving climate change?The Alinker began with BE’s mum not wanting to use a medical mobility aid. Actually, from that it turned into something far larger. Mobility devices are a technical item for a body with a problem. An Alinker makes you feel tall. It puts you at eye level. Veganism and vegetarianism. The meat industry. Awareness. Is an illness caused by environment? Or is it a factor? Building a farm in Kentucky to grow vegetables. Only Alinker users will be on the payroll by 2020. Friendship with Selma BlairHow the Alinker has grown to the level it has. This device is actively making people better. Connect with BE:https://www.thealinker.com/https://twitter.com/TheAlinkerhttps://www.facebook.com/thealinkerUSA/https://www.youtube.com/channel/UC3q2xq_IW56xUXmOKCrIlSg Are you ready to join a secret underground tribe of people that ‘get it’? Search for the ENabled warriors on Facebook to ask your questions in future interviewsOr follow us on Insta: DISabledtoENabled Are you affected by stress? Take the 5-day stress challenge and see if you can live stress-free: free 5 day stress challenge Thank you to Gousto for sponsoring this episode. Please note I do not promote anything I don’t use myself and I can safely say Gousto is my all-time favorite meal box product. I’ve used all the others but this is by far the best in my opinion. Get 60% off your first box and 30% off your first month of boxes (UK only) Click here to get yours: https://mmini.me/goustoDon't just take it from me, here’s what our listener Jo from Coalville, UK says: “Before I used Gousto I made meals purely from the freezer, it was not doing me or my invisible illness any good. This box has taught me how to cook easy meals from fresh every day and my health (and family) thanks me for it - no more mealtime arguments!” - Jo, Coalville. Liven up your dinner tonight with Gousto and have meals like this... Get 60% off your first box and 30% off your first month (UK only) by clicking here: https://mmini.me/gousto
Mentioned in this episode: A marathon runner told to start resting after an MS diagnosis.‘I was afraid because I didn’t know what would happen to me so I just kept going’.Symptoms vs. Marathon running. Cheryl's initial symptoms were painful and strong. She was told by her neurologist to wear an arm cuff to help with electric shock pain. Unsurprisingly it didn’t help. I was given no information about MS at the time of diagnosis. I didn’t know anything about it. I didn’t know it was a central nervous system thing. Despite the MRI showing multiple lesions in my brain but the doctor told her that he couldn’t diagnose her because there was a lack of clinical evidence. Everything I read online was so negative. My husband would find me at 3am googling MS in tears. When I started running again I started noticing problems with my foot. I realised it was a symptom called drop foot. Cheryl went to see her doctor and she told her to ‘lower her expectations’. Cheryl shows us her Ankle-foot-orthotic (AFO) (take a look on youtube) which helps her run with drop foot. Cheryl takes us through her best and worst marathons of all time. Running with her husband by her side, he’s there to stop her drifting off and to open water bottles. Cheryl Hile wants to encourage as many people with MS as possible to join her in her races to prove you can still do anything despite an MS diagnosis. In the last race she did, she got (contact details for Run A Myelin my shoes) I fell in love with running because of Cheryl Hile. Cheryl showed me it was possible. It’s pretty much free, you get outdoors, it minimizes anxiety and depression. My family and friends couldn’t understand that because you can run one day, you can’t necessarily do anything else the next day. How to deal with receiving hate messages. Learning to run when you have the most energy during the day and prioritising your health. People don’t understand that chronic illness conditions fluctuate. The worst thing someone can say to someone else with chronic fatigue… ‘I’m tired too.’Having to leave the job you love because of the diagnosis and when other people are covering up your mistakes due to brain fog, it was time to leave. How Cheryl Hile keeps going alongside marathon running. Cheryl Hile shares her tips on how to get into running. Grab a calendar and start gamifying running.I got started with running via the Couch to 5k app. I did it at lunchtime on weekdays so that there was nobody around. Questions from our ENabled warriors' facebook group. The big question of the episode: How do you manage the potty stops during the marathon?! Find out the weirdest thing Cheryl Hile has ever done… Warning, it’s pretty gross and involves snails. Get in touch with Cheryl:www.cherylhile.com MS Connection blog mention: https://www.msconnection.org/Blog/December-2018/Run-a-Myelin-My-Shoes Cheryl's blog:https://www.cherylhile.com/category/run-a-myelin-my-shoesFacebook: https://www.facebook.com/pink.orbea Are you ready to join a secret underground tribe of people that ‘get it’? Search for the ENabled warriors group on Facebook to ask your questions in future interviewsOr follow us on Insta: DISabledtoENabledAre you affected by stress? Take the 5-day stress challenge and see if you can live stress-free: free 5 day stress challenge____________________________________________________Have you ever felt out of your depth in the kitchen? Do you keep cooking the same thing?Liven up your dinner tonight with Gousto and have meals like this... Get 60% off your first box and 30% off your first month (UK only) by clicking here: https://mmini.me/gousto
Effie from Rising Above Rheumatoid Arthritis (RARA) stops by to discuss all things RA. Starting 14 years ago when she was just a child. Effie was experiencing constant muscle pains, joint pains and inflammation. Fatigue, brain fog and she would come home from school and just sleep. Doctors passed it off as ‘growing pains’. She found herself sitting out more and more at school during gym class. Effie found it harder doing things on her own and she adapted as best as she could but still found it hard to be a young person. Changing her diet practically overnight made things difficult going out with friends. Especially where alcohol is approached. ‘I searched the internet constantly because the internet is the only thing that listened to me.’ Blogs mentioned: The RA guyBarking dog shoes I was expecting my diagnosis so that didn’t scare her but the medication was the thing that really scared her. What helped is throwing the side effects list into the garbage! The main way they diagnosed RA in Effie was by the blood tests and Xrays, the doctor also looked at Effies hands and knew straight away. We chat about the compassion of doctors. During one of Effies trips to the doctor the doctor told her that if she tried an alternative treatment she would be in a wheelchair. She learnt afterwards that he said that because she had a particularly aggressive condition and that it wasn’t advised to not take the medication, however, he could have said it in a much better way! Have you ever experienced a doctors comment like that? Effie wrote and starred in her own documentary. Can you believe someone once called the cops of Effie for parking in a disabled space at a train station? Watch the documentary here: https://www.youtube.com/watch?v=SrdgY1UY0g4&feature=youtu.be She also gives her best advice for working with charities and starting a blog. Effie has worked with so many different charities, organizations and companies. Ever wanted to know more about arthritis? Effie talks us through what it is and the differences between the different types of arthritis. Did you know there are over 100 types? The type Effie has is. Click here to find out more about it: Juvenile idiopathic arthritis Find Effie:Blog: https://risingabovera.com/Facebook: https://www.facebook.com/risingabovera/Instagram: https://www.instagram.com/risingabovera/ Are you ready to join a secret underground tribe of people that ‘get it’? Search for the ENabled warriors on Facebook to ask your questions in future interviewsOr follow us on Insta: DISabledtoENabled Are you affected by stress? Take the 5 day stress challenge and see if you can live stress free: free 5 day stress challenge ____________________________________________________Have you ever felt out of your depth in the kitchen? Do you keep cooking the same thing?Liven up your dinner tonight with Gousto and have meals like this... Get 60% off your first box and 30% off your first month (UK only) by clicking here: https://mmini.me/gousto
Obstetrician and Gynaecologist Dr Jonathan White stops by to discuss all things related to Multiple Sclerosis, Gynaecology, diet, babies, exercise, more babies and lets us in on a few weird gynae things. Topics covered in this episode include: Dr white’s own MS diagnosisHow he deals with working in a busy hospital with MS symptomsHis top advice on diet (and how you can actually eat out at restaurants when you’re following a diet plan! His best tips for exercisingThe miracle of growing a human inside another human (which when you think about it sounds really quite weird?!) The benefits of Vitamin D during pregnancy and how much you should really be taking!How he met his wife over a c-section - how sweet is that?! Jonathan also answers questions from our ENabled warriors facebook group Sharks... Yep, that happened. Connect with Jonny:overcomingMS.org Twitter: @jonty303Instagram: @Jonnywhite1234 Join the ENabled tribe:Search Facebook: ENabled Warriors Or Insta: Enabled_Warriors Get your free messenger gift: bit.ly/5daystresschallenge ____________________________________________________Have you ever felt out of your depth in the kitchen? Do you keep cooking the same thing?Liven up your dinner tonight with Gousto and have meals like this... Get 60% off your first box and 30% off your first month (UK only) by clicking here: https://mmini.me/gousto
In this episode, I invite my mum over for a quick chat about her perspective on what it’s like having a child diagnosed with multiple sclerosis. We discuss what happened from my mum’s point of view at the start of my diagnosis--I didn’t actually tell her what was wrong until I left hospital and was back in my own apartment. Should I have asked her to come to the hospital? Or was I right to not say anything until after? I honestly thought I was helping. My mum describes my diagnosis as a heartbreaking situation that she had no input in and where she was left ridden with guilt for not being by my bedside. We talk about her role as a caregiver to other people with different chronic conditions (some even with MS) who needed full time carers, who were bedridden and one at the stage one lady who needed feeding. My mum told me none of this because she didn’t want to upset me. We also discuss how the care system is faulty with carers not being looked after or supported. Carers do too much and don’t get sufficient financial support My mum and I discuss my first treatment I had - the dreaded injections. I will say, I know plenty of people on this particular treatment who are doing absolutely fine but for me, because I had no fat on my body for the medicine to go into and being drastically underweight, I found it extremely painful and difficult. Mum describes the one time she had to help me do an injection and how she thought it would be easier and more helpful for me to break my ‘injection ritual’ that I created to help me mentally be able to get through each one. She described it like ripping off a plaster. Listen to how that turned out. Funnily enough my brother also had to be called in to help with one, his reaction was hilarious. I asked my mum if anyone had ever suggested any ‘helpful’ holistic advice to her when she told them about my condition and surprisingly she said no. What she said next though, shocked me. She said that plenty of people were asking her about me and how I was coping but not one asked how she was coping with it. At the end of the day this was a huge thing for her too and was probably scarier for her than it was for me actually being diagnosed with the condition. What support is out there for family members who unexpectedly become caregivers? We talk about the 4th annual MS lecture in London and hearing a lot of talks from different sciency people. My mums favourite was Professor Richard Reynolds who explained everything in layman's terms for us non-scientific folk. We learnt a lot there and I met so many people that I thought would make great guests on my podcast. Changing my mum’s sadness on how she thinks my life is and showing her that actually, there is a good side of MS. There is a side that makes me realise I need to live in the present. To appreciate life more. I don’t live with sadness or regret and I didn’t want her to think I lived with sadness and regret. So I think we cleared that up! Social media hides a multitude of sins and an important note is to not believe everything you read online. People only put out there what they want others to see. The delights of invisible symptoms! How do your family and friends react when you tell them about your invisible symptoms. Turns out I have A LOT of family members with chronic illnesses, I had no idea about that until I was diagnosed. Why is this? Why do people not talk about these health conditions? Early signs when I was young that could have been possible MS symptoms? My mum describes how I was ok with ballet because it had structure and a particular choreography but freestyle didn’t come naturally to me--was this because of early poor coordination? Or was I just really bad at freestyle dance? Also, Are you quite softly spoken and quiet? I was, my neurologist said that could also be an early symptom because it showed I was possibly struggling with the energy to make my voice louder. My mum also gives her advice for other parents going throug
Susan Carey - My 21st birthday was at one of my infusions! Topics discussed in this episode:First experiencing double vision. Seeing two golf balls and two basketballs, the optometrist asked her to leave the room while her mum was told there was something in the back of her eye. she could have a tumor or multiple sclerosis. Being officially diagnosed with Multiple Sclerosis - a degenerative health condition at 14A lumbar puncture done by a medical student. (A lumbar puncture is a common test done to diagnose Multiple Sclerosis. It involves extracting some Cerebral Spinal Fluid from between the discs in the spine and testing it) The people in Susan’s Irish village sent her Rosary beads, jumpers and mass cards through the post, was this right to send to a 14 year old diagnosed with MS? She was convinced she was going to die! Treatments and Multiple Sclerosis. We discussed the MS drug Avonex and Susan’s experience with the injectable drug. She was so terrified that her Father kindly stepped in to help her with it. After this she went onto Tysabri (natalizumab) and then Lemtrada (alemtuzumab) - both infusion treatments which means you need to stay in hospital or a few days. With Lemtrada you also need a few days of taking oral steroids before starting the infusion. Susan was told there was not a lot of research done around Lemtrada at the time. The nurse also didn’t know what it meant for fertility something which Susan hadn’t even thought about yet. She was told to go away and Google it, research everything about it that she could find and come to a decision on her own. Susan tells us about how she spent her 21st birthday in hospital doing an infusion and the doctors and nurses left balloons, cake and gave presents which made it far easier for her to deal with. Focussing on what you can do. Every day with her dad Susan would walk the length of the small pier in her hometown. She managed to do this after the Lemtrada treatment without holding on to anything. While she was in hospital, Susan decided she would not miss out on any of her diet or training programme so she packed herself some meals to have in the hospital and made a gym out of what she could find around the ward, like the stairs. Living through your teenage years without being able to do the things you absolutely lived for. Turning the hospital into a gym so she could keep up her fitness routine - even whilst being attached to an IV drip! Planning and prepping her own meals to take into hospital. There is no limitations around you, you can always work around things. Starting her own fitness coaching business after feeling unfulfilled in life called ‘fit fusion’ an inclusive disability fitness program. When the people in your life are supposed to be supportive but just make you feel inferior when you can’t do what they want you to do. A shift.MS takeover made her realise what the hardest part of her illness - family and friends’ unhelpful comments, suggestions and advice. Best advice for coping with Multiple Sclerosis? Suan says to network online with people already talking about their experiences. Tysabri is an intravenous infusion (drip) once every four weeks to reduce the number and severity of relapses. It reduces the number of relapses by about two thirds (70%), compared to taking placebo.Common side effects include dizziness, nausea, urticaria (a skin rash) and shivering.Treatment with Tysabri may increase the risk of progressive multifocal leukoencephalopathy (PML), an uncommon brain infection that can lead to severe disability or even death.(source: https://www.mstrust.org.uk/a-z/tysabri-natalizumab) Lemtrada is a disease modifying drug (DMD) for active relapsing remitting MS and very active relapsing remitting MS.You take Lemtrada as an intravenous infusion (drip) in two treatment courses, twelve months apart. It reduces the number of relapses by about two thirds (70%), compared to taking placebo.Common side effects include infusion-related reactions w
Topics discussed in this episode:Being diagnosed at 10 years old with a mystery skin condition.Spending your teenage years covered in boils, warts and having your fingernails falling off whilst at school. Having a failing immune system and constant bouts of pneumonia at 11 years old.Being so self-conscious at school about having your arms or any skin on show it became normal to cover up - even when in fancy dress costume. Being told at 27 to have surgery to remove a cyst the size of a GOLF BALL in your lung then being told by another doctor not to have the surgery because you might die. Finally being diagnosed with Job’s syndrome* or hyper-IgE syndrome a rare autoimmune deficiency typically occurring in people creating skin and lung issues, also dental issues. Finding a quality research hospitalHaving a lobectomy to remove ¼ of her right lung - even though it was risky and doctors were afraid to.Harper never shared anything with her friends until it was time to have surgery, leave work for a few months Harper didn’t find a community of people for some time but when she did she said it was so incredibly helpful and she wished she found them sooner. Treatment for Harper include daily oral drugs, a nebulizer and every two weeks, an injection. These all help with the functioning of her lungs. What’s the best, worst piece of unhelpful advice you’ve ever been given? Does a diet specific to your blood type really help with my condition that you know nothing about? What is the most annoying thing about having an invisible illness? Probably that it’s invisible. No one gets it. Is it right to self advocate and go against doctors advice when it doesn’t feel right to us?Are meds to override symptoms worth the side effects?Entrepreneurship. Should we all be entrepreneurs? Being a life and business coach and helping people start their own business Want to be an entrepreneur? Ask yourself what you like doing and what you’re good at. Don’t overthink it, just do it. Podcasting is an awesome medium for sharing peoples story’s, whether it be people with chronic illnesses, their caregivers, doctors, wellness practitioners, etc. It keeps it fresh and unique. Top tips for starting your own podcastTop book recommendations: Just Kids by Patty Smith and Chronic resilience by Dana Horne (Job’s Syndrome: Autosomal dominant hyper-IgE syndrome (AD-HIES), formerly known as Job syndrome, is a condition that affects several body systems, particularly the immune system. Recurrent infections are common in people with this condition. Affected individuals tend to have frequent bouts of pneumonia, which are caused by certain kinds of bacteria that infect the lungs and cause inflammation. Inflammation is a normal immune system response to injury and foreign invaders (such as bacteria). However, excessive inflammation can damage body tissues. Recurring pneumonia often results in the formation of air-filled cysts (pneumatoceles) in the lungs. Frequent skin infections and an inflammatory skin disorder called eczema are also very common in AD-HIES. These skin problems cause rashes, blisters, accumulations of pus (abscesses), open sores, and scaling.For unknown reasons, people with AD-HIES have abnormally high levels of an immune system protein called immunoglobulin E (IgE) in the blood. IgE normally triggers an immune response against foreign invaders in the body, particularly parasitic worms, and is involved in allergies. However, IgE is not needed for these roles in people with AD-HIES, and it is unclear why affected individuals have such high levels of the protein without having allergies.AD-HIES also affects other parts of the body, including the bones and teeth. Many people with AD-HIES have skeletal abnormalities such as an unusually large range of joint movement (hyperextensibility), an abnormal curvature of the spine (scoliosis), reduced bone density (osteopenia), and a tendency for bones to fracture easily. A common dental abnormality in this condition is th
Topics covered in this episode:Being a physically fit and active child doing dance and playing hockey before starting in athletics. Kadeena had also done multiple degrees including one in physio which she had to leave 9 months in, due to having a stroke in May 2014. Becoming an MS (Multiple Sclerosis) warrior in September of the same year. Always wanting to be an Olympic athlete and thought she thought she was destined for the 200m sprint. She was then told that to get to an international level she’d have to become a 400-meter sprinter. That’s when things started to go wrong. Kadeena was on the start line of a race but wasn’t able to move her leg. Physio told her it was probably just something tight in her back and to stretch it out. Telling your family and friends from the get-go that you want to be independent and if you need help you’ll ask, but how do you do that in a nice way? How Paralympic classifications are given--there is a lot of testing! The classification process and the differences between the different classifications. Read more about that here Working hard to train for competitions whilst battling extreme fatigue.Disordered eating and how it is affecting training for Kadeena.Going from 10 training sessions per week to being bed bound for 3 months meant Kadeena put on weight that affected her mentally and physically. Female athleticism and the ‘fat-shaming’ pressures female athletes are under when they wear their athletics outfits. The dangers of bulimia, using laxatives and excessive fasting. If you are struggling with issues surrounding eating please take a look at: https://www.beateatingdisorders.org.uk/ and https://www.mind.org.uk/information-support/types-of-mental-health-problems/eating-problems/#.XeJ1spP7QWo Discussing disordered eating issues with friends and family. How they can help. Are fellow competitors friends or foes when it comes to socialising with them outside of athletics events? Being invited on reality TV shows like The Jump and Bake Off. A love of baking cakes for someone who has disordered eating? It’s a thing. Awkwardly meeting Royalty whilst super hungover (oops!) Find out who Kadeena’s favourite royal is and why! What it’s like getting an MBE (which FYI stands for ‘Member of the British Empire’!)How you should live for today because you never know what will be taken away.Kadeena’s favourite book might surprise you.Kadeena’s weirdest thing will definitely surprise you.Why everyone needs to visit Jamaica! The athlete that broke all the rules and lived to win the medals. Follow Kadeena on #Insta and #FaceyB (Kads words, she's cooler than I am!) Read Kadeena’s ‘12 months to Tokyo’ blog. Fact: Kadeena Cox became the first Briton since 1988 to win a medal in two sports at the same Paralympics as she took cycling gold in Rio. Cox, who took T38 100m athletics bronze on Friday, won the C4-5 time trial as Dame Sarah Storey finished fourth.Join the tribe and become ENabled!:Search Facebook: ENabled Warriors Or Insta: Enabled_Warriors Are you affected by stress? Take our 5 day stress challenge and see if you can live stress free click: enabledwarriors.org sign in to messenger and click ‘get started’ to start the challenge.
In this episode, we discuss a lot about pregnancy including Beccy’s advice for having a baby with Multiple Sclerosis! Have you heard of the ‘crazy sheep thing’ that makes womb sounds? How are you supposed to react when the same people give you the ‘helpful advice’ (that FYI doesn’t work) over and over!How can you find other mums going through pregnancy at the same time? The tips and tricks Beccy has for looking after a baby with MS. Connect with Beccy hereOr go to Instagram.com/BeccyhuxtableBeccys TwitterOr go to: https://twitter.com/beccyhuxtable Read Beccy’s articles on multiple sclerosis here:https://www.mssociety.org.uk/authors/beccy-huxtable https://www.express.co.uk/life-style/health/420646/I-discovered-I-had-multiple-sclerosis-live-on-the-radio?fbclid=IwAR2Tv5Hdg4dxKhsD1nli6ZxJ4Nla-WehctOLIl3c7nvW3aMwgWCZLcuSJ2o Scott and Beccy go behind the scenes of MS research: https://www.youtube.com/watch?v=5bNsrr1afeI Join the ENabled tribe:Search Facebook: ENabled Warriors Or Insta: Enabled_WarriorsAre you affected by stress? Take the 5-day stress challenge and see if you can live stress-free bit.ly/5daystresschallenge
Topics covered in this episode:First MS symptomsBeing predisposed to addictionEndometriosis Postpartum depressionBeing a counselor in a prisonSetting up a businessHow can people with chronic illness heal? Connect with Shelley:Website: https://www.shelleyramseydejongh.com/Instagram: https://www.instagram.com/shelley_ramsey_dejongh/Facebook: https://www.facebook.com/shelleyramseydejonghteletherapy/ Join the ENabled tribe:Search Facebook: ENabled Warriors Or Insta: Enabled_WarriorsGet your free messenger gift: bit.ly/5daystresschallenge
Meet Heather... She takes on her illness everyday alongside her quirky prehistoric knitted companion, Dizzy! She was diagnosed at 25 with Multiple Sclerosis and runs one of the coolest blogs I have ever seen - Dinosaurs, Donkeys and MS. She’s taking on the world of chronic illness - one donkey at a time. She’s here with us today. ENabled warriors please help me in welcoming our next guest, the amazing… Heather Russell-Kay and Dizzy! Things we discussed in this episode:Heathers first MS relapseMisdiagnosisSelma BlairThe complexities of MSCan our partners help us know when to stop?Dizzy’s roots at the Sidmouth Donkey sanctuaryWhat does a tattoo really feel like? Tips for getting a tattoo with MSShift.MS for young people newly diagnosed Link with Heather and Dizzy!www.dinosaursdonkeysandms.comFacebook.com/DizzytheddonkeyInstagram.com/DizzytheddonkeyTwitter.com/Dizzytheddonkey Join the ENabled tribe:Search Facebook: ENabled Warriors Or Insta: Enabled_Warriors Can you handle the stress? Take the FREE 5day stress challenge now in Facebook Messenger! Click: bit.ly/5daystresschallenge
Topics covered in this episode: Gina’s experience of a heart attack. Children going missingWhat is angina? How is Angina detected?MigrainesDealing with your ex bad mouthing you to your children about your illnessThe benefits of working for yourselfGina’s awesome podcast - ‘Life’s valleys and mountain tops’ Wait till you hear about the weirdest thing Gina has ever done! (Hint: It involves a bus, a paedophile and a newspaper) Catch up with Gina at:www.Synergymindsetcoaching.comOn facebook: /ginaamjohnsonOr Insta: @synergymindsetcoaching You can also hear DISabled to ENabled podcast host Jessie Ace being interviewed on Gina’s podcast here Join the ENabled tribe:Search Facebook: ENabled Warriors Or Insta: Enabled_Warriors Get your free messenger gift: bit.ly/5daystresschallenge
Actress Ciena Rae stops by to chat about the issues that come with being an Actress and having Psoriasis and eczema with the added pressures of constant reapplying of make up, photoshoots and close up camera shots alongside the pressures of being in the public eye. Ciena Shares her tips for other people suffering with Psoriasis and eczema and tells us about her daily routines that lead her to keep control of her skin. Also, wait till you hear about the documentary she is currently recording to help people with chronic illnesses and the advocacy work she’s currently doing. We think she’s the total psoriasis BOSS. Get your shout out on the podcast by pledging a dollar and get free perks! http://bit.ly/enabledsupport or leave a rating and review :) Want to manage your symptoms without taking extra meds for free? Get your FREE digital download here: bit.ly/enabledebook Connect with Ciena Rae:Website: www.CienaRae.comInstagram: @CienaRae Join the ENabled tribe:Search Facebook: ENabled Warriors Or Insta: Enabled_Warriors
“You can find a lot of good things in something broken” - Chanel White 2019Do not listen to any other podcast until you’ve listened to this one. Chanel keeps it real and takes us through what was like when she won the chronic illness lottery. Going from what started as ‘burnt black pus fingers’ on her wedding day to complete organ failure and being tube fed. We go into detail about how her body functions (or not) day to day and how she gets though that with a dark sense of humour and an infectious laugh. Find out why she scares medical students and why her mother in law decided to start charging medical students for photos. Also, hear about the time she made doctors hate her when she decided to go sky-diving and about that time she went riding an Ostrich. [DISCLAIMER] This episode contains too much information, feelings of nausea and unexpected stories. P.s. Bonus! See if you can catch the BIGGEST mistake I have ever made in an episode!! [Warning: includes hilarious results] Get your shout out on the podcast by pledging a dollar and get free perks! http://bit.ly/enabledsupport or leave a rating and review :)Want to manage your symptoms without taking extra meds for free? Get your FREE GIFT here: bit.ly/enabledebook Blog: TheTubeFedWife.blogspot.comInstagram: @TheTubeFedWifeFollow the ENabled warriors and join the tribe!Facebook: ENabledwarriorsInstagram @ENabledwarriors Don’t forget to click here for your FREE GIFT! (Check your Facebook messenger after clicking)
Jenny Clarkson from the wonderful blog Tripping through Treacle stops by to tell us her experiences of Secondary Progressive MS starting at just 15 years old. Can you imagine having your body go out of control at such a young age? She tells us about what it was like to get such a big, life changing diagnosis when she was still so young, even describing her experiences of relapsing at prom and having to get her boyfriend to hold her up by her arms all night so she could walk. We also discuss the new HSCT (stem cell) treatment that is the new treatment on the block, what it actually is, the criteria for it and what Jenny’s experiences were of it. Did you know they extract stem cells from your bone marrow?! shudders Finally, learn what life hacks she has built up to be able to cope with Secondary Progressive MS whilst raising two beautiful kids. Speaking of kids we also discuss what it it’s like having kids whilst having MS. Find out the hardest thing Jenny had to talk about with her children that made her totes emosh. Yes, I just said ‘totes emosh’ - i'm down with the kids. I went there. Get your shout out on the podcast by pledging a dollar and get free perks! > http://bit.ly/enabledsupport or leave a rating and review :) Want to manage your symptoms without taking extra meds for free? Get your FREE GIFT here: bit.ly/enabledebook Connect with JennyMain site: https://trippingthroughtreacle.com/Facebook: https://www.facebook.com/trippingthroughtreacleInstagram: https://www.instagram.com/trippingthroughtreacle/Twitter: https://twitter.com/trippingtreacleFollow her SPMS and HSCT journey through Youtube: https://www.youtube.com/channel/UCnqkX6oYTSzfbm7pj_lWSCw/videos Don’t forget to click here for your FREE GIFT! (Check your Facebook messenger after clicking)
Sandy Bista drops by to discuss all things Fibro. We discuss the importance of mindset when you have a chronic illness because if you don’t have a strong mindset you won’t necessarily live a happy life where you achieve your goals. Sandy also tells us about how she had to go to India from Australia to get a diagnosis of Fibromyalgia after her doctor in Australia told her she ‘wouldn't have Fibro because she was too young’. Want a FREE GIFT? Reduce your symptoms without taking extra meds. Click here: bit.ly/enabledebook Get a shout out on the podcast! Click here to pledge a few dollars > http://bit.ly/SupportWarriors Sandy tells all about her diagnosis process, how fibro is diagnosed, what Fibro feels like and the stigma that unfortunately comes with it. How does she cope with running an events business with her sister whilst fighting Fibromyalgia? Sandy discusses her coping tips she’s developed. Finally, her biggest dream is to create a community of people who can be open about their struggles whether it be with mental health, or fibromyalgia or anything. That is a safe, happy place where people can share their concerns and be listened to. Somewhere where their story really matters. Connect with Sandy here: Good Vibes Events: https://www.goodvibesevents.com.au/eventsInstagram: Instagram.com/Happimindset Facebook: https://www.facebook.com/Happimindset/ Join the ENabled tribe:Search Facebook: ENabled Warriors Or Insta: Enabled_Warriors Want a FREE GIFT? Reduce your symptoms without taking extra meds. Click here: bit.ly/enabledebook Get a shout out on the podcast! Click here to pledge a few dollars > http://bit.ly/SupportWarriors
Dara drops by from ByZantine Design to discuss everything MS, what she’s learnt since having the illness and tells us about some ‘hacks’ she’s picked up since diagnosis. We discuss the important topic that is ‘normal business hours’ not being inclusive to members of the chronic illness community. Why can’t there be more flexibility with a ‘normal working day’ in a business? We discuss the importance of a morning and evening routine when you have a chronic illness and the especially important-making of your bed! We also discuss what it was like for her to open her first store whilst having her first MS symptoms and trying to battle those around hospital appointments, finding staff and negotiating numbness. If you’re watching this interview on Youtube you may spot Fergus, her ‘paw-sitive’ 4 legged companion! (he’s gorgeous!) Want a shout out on the podcast? Click here to pledge $5 and get free perks! > http://bit.ly/enabledsupport or leave a rating and review :) Want to manage your symptoms without taking extra meds for free? Click here: bit.ly/enabledebook Connect with Dara at https://byzantinedesign.com.au/Or Insta: @byzantine_design Or go to A chronic entrepreneur: https://achronicentrepreneur.com Facebook: https://www.facebook.com/achronicentrepreneur/Insta: https://www.instagram.com/achronicentrepreneur/ Join the ENabled tribe:Search Facebook: ENabled Warriors Or Insta: Enabled_Warriors Want a shout out on the podcast? Click here to pledge $5 and get free perks when you become our patreon! > http://bit.ly/enabledsupport or leave a rating and review :)
We chat to 7.5x Ironman Champion Conor Devine to get the lowdown on his adventures with Multiple Sclerosis, neurologists, a plant based diet, managing a business, kids and oh yeah, competing in the biggest challenge a person can do - the IRONMAN CHALLENGE. This extraordinary warrior defies the odds everyday using food and exercise as his medicine. Conor is an author with two incredible books, ‘Attitude is everything’ detailing his journey with his diagnosis and ‘Ironmind: against all odds’ detailing his journey getting to his first ironman challenge. We talk a lot about Conor’s incredible plant based diet and how he handles social events. How does he make fruit and veg interesting enough for not only himself to have each day but for two young children too. Want to manage your symptoms without taking extra meds for free? Click here: Free digital download book Want a shout out on the podcast? Click here to pledge $5 and get perks! > http://bit.ly/enabledsupport or leave a rating and review :) Connect with Conor Devine at www.ConorDevine.comSearch for him on social media Join the ENabled tribe:Search Facebook: ENabled Warriors Or Insta: Enabled_Warriors Want a shout out on the podcast? Click here to pledge $5 and get perks! > http://bit.ly/enabledsupport or leave a rating and review :)
Scott Mills reveals some interesting truths about his experiences with invisible illness including the time he accidentally diagnosed his ex-assistant Becky whilst live on air. We chat about the power of staying positive and how to achieve things you never thought you could. We also talk about the time he dressed up as a crab on Strictly Come Dancing and starred in his own musical. Get a shout out in a future episode by becoming an ENabled Hero! Click here: bit.ly/enabledhero and click 'become a patreon' Listen to Scott Mills live on Radio 1 Monday-Thursday 1pm-4pm and as he does the official chart show on Friday 4pm-7pm. Catch up on previous episodes of the Scott Mills show on the BBC website: https://www.bbc.co.uk/programmes/b006wkt4/episodes/player Or listen to all of Scott’s show (without the music) on his podcast including Innuendo Bingo, prank calls, Chris’s stories, listeners’ dilemmas, Real Or No Real and stupid games. Listen on the BBC website or click here: https://www.bbc.co.uk/programmes/p02nrv1j/episodes/downloads Get a free digital download to reduce your symptoms without taking more medication! Click here: bit.ly/enabledebook Join the tribe of warriors:Search Facebook: ENabled Warriors Or Insta: Enabled_Warriors Get a shout out in a future episode by becoming an ENabled Hero! Click here: bit.ly/enabledhero and click 'become a patreon' Stay #ENabled
Alicia Aiello stops by to discuss all things IBD’s stomas, surgeries and POOP! We clear up the myths around IBDs, sex, pregnancy, dating and periods - it’s not an interview for the faint hearted! We also discuss her best advice for coping with constant IBD surgeries, the real risks of taking short term steroids (ever heard of bone death?!) and the glorious retreats held by the fabulous Girls With Guts. Alicia is president of ‘Girls With Guts’ which is an organisation which helps women become empowered, knowledgeable and their own advocate for their healthcare. They recognise that women in particular have a more difficult time with IBDs because of all that added biology and social pressure. They do a great job of supporting women with IBDs with their retreats, butt baskets and ‘gotta go’ cards. Make sure to check out their website if you have an IBD. Want a shout out on the podcast? Click here to pledge $5 and get perks! > http://bit.ly/enabledsupport or leave a rating and review :)If you’re watching on YouTube you may also see a special kitty guest! Connect with Alicia, president of Girls With Guts at GirlsWithGuts.org Thanks to Audible for sponsoring this episodeGet a free audio copy of the book ‘Brain on Fire’ mentioned in this podcast episode by clicking here: http://bit.ly/enabledwarrior Join the tribe of warriors:Search Facebook: ENabled Warriors Or Insta: Enabled_Warriors Want a shout out on the podcast? Click here to pledge $5 and get perks! > http://bit.ly/enabledsupport or leave a rating and review :)Stay #ENabled
Were you given enough information when you were diagnosed? Trishna describes the moment she was diagnosed as like being left to fend for herself in a black hole. From here she decided to take matters into her own hands and start writing for various charities, magazines and blogs. In particular, she writes for the Asian MS community in which there is a lot of stigma to break through. Soon, she was being invited to speak at events all over the world. She somehow does all of this while also working full time as a translator and analyst, doing regular zumba dance classes and appearing on TV shows like the People’s Strictly Come Dancing. How she fits all this in on top of having MS - I have no idea! Thankfully she does and thank goodness she does because she’s changing the lives of so many people. Hear patient advocate and inspirational speaker Trishna Bharadia talk about everything from the problems in our health care industry to what it was like to be on the People’s Strictly Come Dancing. If you’re watching on YouTube you may recognise Trishna? Catch Trishna’s sister Anisha on an earlier episode of the DISabled to ENabled podcast. Want a shout out on the podcast? Click here to pledge $5 and get perks! > http://bit.ly/enabledsupport or leave a rating and review :) Thanks to Audible for sponsoring this episodeGet a free audio copy of the book ‘A simplified life’ mentioned in this podcast episode by clicking here: http://bit.ly/enabledwarrior Join the tribe of warriors:Search Facebook: ENabled Warriors Or Insta: Enabled_Warriors Want a shout out on the podcast? Click here to pledge $5 and get perks! > http://bit.ly/enabledsupport or leave a rating and review :)Stay #ENabled
What would you do if you were constantly in a state of high adrenaline from doing nothing? How is it currently treated? Can it be treated in a different way? What is Graves disease? Faith found herself in a struggle during college when she suddenly lost a crazy amount of weight for no reason, had crazy adrenaline rushes all through the day leaving her unable to sleep. Being in a constant state of stress is so damaging to the body. The medication she was put on by doctors - radioactive iodine - which was designed to kill her thyroid also in the process gave her cystic acne and made her more susceptible to mould poisoning. But could there have been a better way to treat it? She found that after taking her care into her own hands and looking after her body from a natural point of view she became a lot better and her condition became manageable. Her cystic acne on her face soon cleared up after she experimented with cutting out dairy. Not once was this suggested by her dermatologist who kept pushing pharmaceuticals on her. Are pharmaceutical companies helping or hindering our overall health? We talk about the problems in our health care industry and also our education system after she was put on Adderall throughout her childhood. It raises the question: Should children take amphetamines like Adderall and Ridilin? Is it just a ploy for schools to get better grades? Connect with Faith at:www.thathealing-feeling.com Instagram: @thathealingfeeling Thanks to Audible for sponsoring this episodeGet a free audio copy of the book ‘A simplified life’ mentioned in this podcast episode by clicking here: http://bit.ly/enabledwarrior Join the tribe of warriors:Search Facebook: ENabled Warriors Or Insta: Enabled_Warriors Want a shout out on the podcast? Click here to pledge $5 and get perks! > http://bit.ly/enabledsupport or leave a rating and review :)Stay #ENabled
After suffering a mini stroke at just 14 years old, life hasn’t quite been the same since for blogger Sheryl Chan. Now living with 5 chronic conditions everyday is a different mix of symptoms. Who knows what she’ll wake up with tomorrow? That however, doesn’t stop her from writing her awesome and inspiring blog, ‘ Chronic Voice’ where she talks about everyday life with so many challenges, how she overcomes them and how she inspires others to live with their own chronic conditions. Sheryl Shows us that anything is possible if you set your mind to it. Listen to her crucial life advice for people with chronic illnesses - particularly if you live in Singapore. She once had a taxi driver tell her a quote she’s never forgotten: ‘You can die in Singapore, but you can’t get sick - it’s too expensive’. We discuss the crazy laws around health and disability in Singapore and how she manages it with all of her life saving medications. What emotional impact does that have on a chronically ill person? Listen to her interview to find out. Connect with Sheryl Chan:Blog site: https://www.achronicvoice.com/Twitter: https://twitter.com/AChVoiceInsta: https://www.instagram.com/achronicvoice/Thanks to Audible for sponsoring this episodeGet a free audio copy of the book mentioned in this podcast episode by clicking here: http://bit.ly/enabledwarrior Join the tribe of warriors:Search Facebook: ENabled Warriors Or Insta: Enabled_Warriors Want a shout out on the podcast? Click here to pledge $5 and get perks! > http://bit.ly/enabledsupport or leave a rating and review :)Stay #ENabled
Tips from a doctor for how to deal with the heat when you have an invisible illness and the benefits of neuroplasticity. Did you also know there are two types of relapses? Where do doctors go to nerd out on new scientific advances? How can doctors be helping people with MS virtually with exercise, mindset and accountability? Dr Gretchen really is the future of doctors y’all! Also, wait till you hear what her weirdest moment was… WARNING It may make you queasy! Want a shout out on the podcast? Click here to pledge $5 and get perks! > http://bit.ly/enabledsupport or leave a rating and review :) PLUS - This episode is sponsored by WrapMeCool. If you want something that can keep you cool when you're hot under the collar this summer, try a WrapMeCool. It looks like a normal scarf but acts like a cooling vest.Get 10% off the ultimate summer essential cool shawl wrap that keeps you cool whilst looking normal.www.WrapMeCool.comUse the code EW19 Connect with Dr. Gretchen:Youtube: Search Doctor Gretchen HawleyEmail: gretchen@doctorgretchenhawley.comWebsite: www.MSinglink.com Insta - @Doctor.gretchenFacebook - Doctor Gretchen MS Specialist Get a free audio copy of the book The Miracle Morning mentioned in this episode by clicking here: http://bit.ly/enabledwarrior Join the tribe of warriors:Search Facebook: ENabled Warriors Or Insta: Enabled_Warriors Want a shout out on the podcast? Click here to pledge $5 and get perks! > http://bit.ly/enabledsupport or leave a rating and review :)Stay #ENabled
We discuss everything from a rare immune disorder I can’t even pronounce (panhypogammaglobulinemia), being a pageant queen, charity fundraising the joys of Infusion treatments and how to survive a hospital visit. Jayde fills us in on how she created her own business at the age of 22 planning events including celebrity clients whilst battling her rare immunodeficiency disorder that even doctors have to search the internet about. Insta: @JandJEventplanning Facebook: /jandjeventplanning1Search: J&J event planning Lichfield Facebook: ENabled Warriors Insta: Enabled_WarriorsGet the featured book mentioned in this podcast for free! Click here: http://bit.ly/enabledwarriorWant a shout out on the podcast? Click here to pledge $5 and get perks! > http://bit.ly/enabledsupport or leave a rating and review :)Stay #ENabled
We get the lowdown on what exercise REALLY does to someone with an invisible illness and why it’s worth pushing through that fatigue!. Why you should stop buying exercise equipment from infomercials. We talk about inclusive fitness with expert Dom Thorpe from Disability Training. He discusses why all gym instructors should be inclusive. We’ll also discuss tips to get your body (and mind) healthy and living your best life. Want a shout out on the podcast? Click here to pledge $5 and get perks! > http://bit.ly/enabledsupport or leave a rating and review :) Connect with Dom Thorpe:Click DT Disability Training or search (dt-training.co.uk/) Join his Facebook group here Or search for multiple sclerosis (ms) fitness & exercise motivation with Dom ThorpeFacebook page search Dom Thorpe If you love this podcast please subscribe and leave a rating and review if you think it’s good enough. Facebook search enabled warrior or click here: ENabled Warriors Insta search: @Enabled_Warriors Want a shout out on the podcast? Click here to pledge $5 and get perks! > http://bit.ly/enabledsupport or leave a rating and review :)Get the book mentioned in this podcast for free! Click here: http://bit.ly/enabledwarrior Stay #ENabled
Anisha tells us how zumba saved her mental health, the shocking and incredible story of how her PTSD was first caused. Tips for travelling with Ulcerative Colitis (and every other one of her conditions!). Anisha is an incredible inclusive dance teacher with a family that has different autoimmune conditions. Listen to her incredible story on the DISabled to ENabled podcast. Connect with Anisha, search:Website: Zumba with Anisha GFacebook: Zumba with Anisha Facebook If you love this podcast please subscribe and leave a rating and review if you think it’s good enough. Facebook: ENabled Warriors Insta: Enabled_Warriors Get a free audiobook, click here: http://bit.ly/enabledwarriorWant a shout out on the podcast? Click here to pledge $5 and get perks! > http://bit.ly/enabledsupport or leave a rating and review :)Stay #ENabled
We discuss the ins and outs of the new stem cell treatment for MS and how Jess will be posting everything about her journey with it live on her Instagram (link below). We also discuss what she does for the MS Society in Canada and Jess also shares her best advice for nutrition and exercise that she’s learnt from her 2 degree qualifications in dietetic science and holistic nutrition and with living with MS since she was 15 years old. She’s a runner and boxer whilst fighting through chemo. She’s incredible.Connect with Jess (and follow her stem cell treatment)Insta: @AlltherightbitesTake a look at ‘Wrap me cool’ and use code JESS for a 5% discountIf you love this podcast please subscribe! And leave a rating and reviewJoin the warrior tribe here Facebook: ENabled Warriors Insta: Enabled_WarriorsRead Jessie Ace's blogs here: www.JessieAce.com Want a shout out on the podcast? Click here to pledge $5 and get perks! > http://bit.ly/enabledsupport or leave a rating and review :)Stay #ENabled
We talk to Leslie Touchton about her MS diagnosis and hows she’s come to terms with it and told it ‘no’. Leslie lives an amazingly active lifestyle and she shares with us her tips for energy management and the importance of goals to live a life that’s full and awesome. We also discuss how she’s managed to continue running despite having heavy foot drop feet! Connect with Leslie:Here: https://www.facebook.com/leslie.touchton.1 If you love this podcast please subscribe! Comment below with who else you would like to see interviewed. And join the tribe! Facebook: ENabled Warriors Insta: @jessieaceofficialwww.jessieace.com Don't forget to leave a rating and review
What happens when you get a creative inventor mixed with an invisible illness? A lot of cool stuff to help ENabled people to live their best lives possible! We also discuss Jessica's travel tips and stories of when she travelled ALONE around the world with an invisible illness! Say what?! Public speaking events and how’s she’s teaching businesses to include disabled people instead of fearing them. Connect with Jessica:Twitter - @D_DisabilityInstagram - @D_Disability Facebook - Design for DisabilityLinkedIn - Design for DisabilityAnd her main website http://designfordisability.co.uk If you love this podcast please subscribe! Comment below with who else you would like to see me interview! And leave a rating and reviewAnd join the tribe! Facebook: ENabled Warriors Insta: Enabled_Warriorswww.jessieace.com
Senior Content Development specialist for MSConnection.org blog Christy Kim talks to us about everything she’s learnt from the reading the blogs written by people with MS. We talk about our love of writing and reading, how invisible symptoms are portrayed by the public and how people with MS can be better together. Episode #6 Connect with Christy:Insta - @Clhkayy www.MSConnection.org If you love this podcast please subscribe! Comment below with who else you would like to see me interview. And leave a rating and reviewAnd join the tribe! Facebook: ENabled Warriors Insta: Enabled_WarriorsWebsite: www.Jessieace.com
In this special podcast episode, you'll learn what the DISabled to ENabled podcast is all about and who the heck is Jessie Ace? I hope you love this podcast as much as I loved making it. There was nothing like this when I was diagnosed at 22 years old. Follow the warrior tribe!If you love this podcast please subscribe! Comment below with who else you would like to see me interview. And leave a rating and reviewAnd join the tribe! Facebook: ENabled Warriors Insta: Enabled_Warriorswww.jessieace.comWant a shout out on the podcast? Click here to pledge $5 and get perks! > http://bit.ly/enabledsupport or leave a rating and review :)Stay #ENabled
The new CEO of the MS Society Mr Nick Moberly answers your questions asked across social media groups. We discuss his plans for the future of the MS Society - and they might surprise you! He answers topics such as: how we can give people a voice in the community? What help and support needs to be improved, particularly for young people? And how is that £5million budget allocated between the different areas? Also we discuss why you need to campaign to get your voice heard. Episode #6Follow Nick:MSSociety.org.ukIf you love this podcast please subscribe!And leave a rating and review if you think it's good enough,Click the links below to join the tribe!Facebook: ENabled WarriorsInsta: Enabled_Warriors
HR manager at Tesco turned social media legend Kaz Laljee has fully embraced his MS diagnosis setting up not only his social media business (Soc-Med.com) but also his site ‘Positive About MS’ he continues to push the limits of his primary progressive MS. We discuss everything from energy hacks to combat fatigue, how to discuss MS with your kids using ‘The Simpsons’ and why you shouldn’t use toilet rolls for bowling in supermarket aisles! Follow Kaz:Instagram - @positiveaboutMSFacebook - @positiveaboutMSEmail - kaz@positiveaboutms.comWeb - www.positiveaboutms.com If you love this podcast please subscribe! And leave a rating and review if you think it's good enough,Click the links below to join the tribe! Facebook: ENabled Warriors Insta: Enabled_Warriors
Gary Pinder explains how he took his MS diagnosis and made it into something extraordinary. We talk about everything from medications, how Gary told his kids he had MS and how he managed a trip to Everest Base Camp. We also discuss how to stay cool when exercising with an invisible illness. Remember if you like this podcast click the subscribe button and keep up to date! You can also follow the ENabled Warriors on Facebook, Instagram and Youtube - just search - ENabled Warriors.Follow Gary here - @MSThrivers
Marisa says NO to her MS. She goes running, works out, does marathons. She’s even set up the movement Fight for Mobility to inspire others living with an invisible illness. We talk bad English accents, humorous MS bathroom issues and her ultimate warrior mindset hacks. Let’s focus on what you are able to today. “What are you able to do today? Have those words be ‘I can’” Follow Marisa:Instagram - @RisamoeYoutube - https://www.youtube.com/channel/UCXIFDrb0ihtyl2joYIBPraQ Subscribe to the podcast if you’ve been inspired.And join the tribe! Facebook: ENabled Warriors Insta: Enabled_Warriors
The creator of the face for The National MS Society tells all about how the National MS Society’s brand has evolved over the last few years, how the role of photography is especially important because nobody wants to be the face of bladder issues! BUT illustration is also important! And how the NMSS create ‘anti-victim’ advertising. Follow the National MS Society: https://www.nationalmssociety.org/Follow the NMSS behind the scenes and Marks adventures on Insta - @Mark_Serratoni Subscribe to the podcast if you’ve been inspired!And join the tribe! Facebook: ENabled Warriors Insta: Enabled_Warriors
Nora explains how her MS diagnosis at age 35 made her want to lose weight, why (and how!) she started running marathons, how she manages her energy around marathons and that story about the time she had to pee at the side of the road (we’ve all been there, right?) Catch up with Nora here: Nottodayms.comfacebook.com/nottodaymsInsta - @nottodayMs1 Join the tribe!Facebook: ENabled Warriors Insta: Enabled_Warriors