The Princess of Possible: Recent Episodes
Emmah Money
The Princess of Possible, a podcast that is real, raw and authentic providing education and inspiration through real stories of strength, courage and determination.
Join Emmah, this year’s 2020 SA Local Hero, Mother of two, Author and Cystic Fibrosis Advocate as she embarks on an intimate journey. She not only opens up about life challenges and how she has overcome adversity and become the ultimate resilience Princess, but is joined by a diverse range of guests living with Cystic Fibrosis, making the impossible...POSSIBLE. And let’s just say don’t know exactly what they are in for when it comes to talking to Emmah.
With Emmah’s quirky personality, she is not afraid to ask the “do not ask” questions as she gets up close and personal with her guests.
Captivating audiences through honesty and vulnerability it will take empowerment to a whole new level.
Imagine after 9 long months, the day has finally come and your beautiful baby was placed in your arms, yet only to learn within days they have been diagnosed with Cystic Fibrosis. Like many, you want to do your own research, so many questions fill your mind. So you head to google.com and type in Cystic Fibrosis, only to see the search results come up with the most scariest and confronting facts and statistics, leaving you beyond disbelief as you fear for the life your child may or may not get to live.
Whilst CF does not define someone, it sure as hell comes with interruptions to the lives of those living with CF. I had the pleasure of speaking to the beautiful Cassie Day, about what it is like to be the mother of a child with Cystic Fibrosis.
Cassie openly talks to me about her son Matthew who has Cystic Fibrosis and the effects CF has had on her entire family.
We talk about the mothers perspective on hospital admissions, medical appointments, the guilt and heartache and just how to "hand the baton" to her adult child at just 18, after fighting for him and his health his entire life, allowing him to now take over his health.
What a remarkable story of Cassie and her boys, as CF may have caused some hiccups, but it has not let anything get in their way!!! The ultimate family, making the so called google result "impossible" and turning those unexpected milestones into possible a million times over!
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When I first saw that Nathan Charles had Cystic Fibrosis, it took me by surprise. Why? It is not everyday you would see a CF male with muscles like his!
The former Australian rugby union player is on a mission to create a wider awareness of Cystic Fibrosis and to inspire people to overcome adversity.
Nathans laid back, charismatic self had me blushing, as we speak about living with Cystic Fibrosis. I was surprised to learn that at the beginning of his Rugby career, he had not told his coach he had Cystic Fibrosis... How was this even possible? Playing at an elite level, yet CF not being known to his team mates and coaches.....
This interview was funny, real and raw.... but ever so inspiring!!
Nathan, you are a bloody legend and I am grateful to share your story to the world!
Thank you for trusting me in this unscripted conversation!
Independent woman, Rebekah Papadatos joins me as we talk about CF, body image, career, relationships... actually I don't think there is anything we don't talk about. When you learn about what Bek's career path is... like many, you might be in a bit of shock. Having grown up in hospitals most of her childhood, to spending a lot of her adulthood visiting the doctors, from a young age Bek knew she wanted to become a nurse.
Despite the "risk" it may have on her CF, Bek is a proud Registered Nurse.
With so much to talk about, we could have spoken for hours, however lets just say we kept it to the juicy stuff and this episode is as real as it gets..
Harry Coffey is like no other, I couldn't believe the similarities in our CF when it came to our treatment as a child, to the "battles" of being a CF adult. What particularly stands out, is Harrys "anything is possible" attitude. Despite the hurdles he faces living with CF, this does not stop Harry from doing what he loves.
"From spending days in hospital getting his 'grease and oil change' and taking over 30 pills a day, just to keep everything in check, this story will introduce to you a young man living his dream"
In the words of Neil Kearney: (Victoria-based journalist)
'A story that transcends racing, a young man with a terminal illness who refuses to be beaten.'
'His doctors never wanted him to be a jockey but now they cheer every ride.
'Harry Coffey is an inspiration, a remarkable Australian.'
Get the tissues ready because this was one had even me in tears. Meet Jackie Fraser, founder of Rose Lungs clothing and Cystic Fibrosis boss babe. Through using her social media platform to raise awareness for Cystic Fibrosis and Organ Donation Jackie is not afraid to tell it how it is.
After being advised by her medical team that a transplant was on the cards, Jackie and her dear husband Aidan put "life on hold" as they packed up and caravanned around Australia, with an oxygen tank, living her last days to the fullest.
Join me as we talk about "That Call", feminism and body image, of course, Cystic Fibrosis , where I ask the questions that we all want to know the answers to yet are fearful to ask.
This season you will meet Cystic Fibrosis warriors who have made the "impossible" POSSIBLE.
Meet Kyle Collis. aka The CF Fighter. A husband, father of two and marathon runner. Thats right, a Cystic Fibrosis marathon runner! Kyle's life has been nothing short of interruptions no thanks to Cystic Fibrosis, however this has not stopped him from living his life to the fullest. Join me as we talk about growing up with Cystic Fibrosis and the challenges, the death of many CF friends, become a Cystic Fibrosis father, OH! And those life changing drugs that he has now started taking that has given him a whole new lease on life!
For more information Insta: @Theprincessofpossible www.cfmummy.com.au