The Michael J. Fox Foundation Parkinson's Podcast: Recent Episodes
Michael J. Fox Foundation
Subscribe for coverage and analysis of current neurology/brain research, patient and caregiver profiles, drug development strategy, pioneering nonprofit management and other topics of interest in a wide-ranging series of conversations that include the voices of those affected by Parkinson's as well as clinicians.
Parkinsonism is an umbrella term to describe a group of conditions that cause movement symptoms. Parkinson’s disease shares some traits with drug-induced and vascular parkinsonisms, as well as atypical parkinsonisms, but each condition differs in how it progresses and is treated. Listen to audio from this month’s MJFF Parkinson’s Webinar to hear our panel of experts discuss the sometimes-long path to diagnosis and what people with parkinsonism and their families should know. They also cover the latest research into parkinsonisms.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
Whether you have Parkinson’s or not, you can help move research forward. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
Mentioned in this episode:
Researchers are studying the link between sense of smell and brain health. People with and without Parkinson's can help by taking a scratch-and-sniff test. It’s free, mailed to your home and takes just 15 minutes to complete.mysmelltest.org/getstarted
Better treatments for Parkinson’s disease depend on increasing our understanding of why Parkinson’s develops and how it progresses. The Michael J. Fox Foundation’s landmark study, the Parkinson’s Precision Medicine Initiative (PPMI), is expanding to better answer those questions.
In this episode of The Michael J. Fox Foundation Parkinson’s Podcast, Maggie Kuhl, vice president of patient engagement at MJFF, leads a conversation about these efforts with:
- Kenneth Marek, MD, co-founder of the Institute for Neurodegenerative Disorders and PPMI’s principal investigator
- Sohini Chowdhury, MJFF’s chief program officer
- Donna Rajkovic, who was diagnosed with Parkinson’s disease in 2012 and joined PPMI the same year
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
The Foundation’s landmark study, the Parkinson’s Precision Medicine Initiative, also known as PPMI, is recruiting volunteers. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi
Mentioned in this episode:
Researchers are studying the link between sense of smell and brain health. People with and without Parkinson's can help by taking a scratch-and-sniff test. It’s free, mailed to your home and takes just 15 minutes to complete.mysmelltest.org/getstarted
Breakthroughs depend on research volunteers, but many people have questions about what participating in a trial means, and how to select the right trial for their goals, needs and lifestyle. Listen to audio from this month’s Third Thursdays Webinar to hear our panel of experts share what to look for in a trial you’re considering and how to navigate the clinical trial process.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
Whether you have Parkinson’s or not, you can help move research forward. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
This webinar received support from BlueRock Therapeutics. Learn more at expditestudy.com.
Mentioned in this episode:
Researchers are studying the link between sense of smell and brain health. People with and without Parkinson's can help by taking a scratch-and-sniff test. It’s free, mailed to your home and takes just 15 minutes to complete.mysmelltest.org/getstarted
Constipation is a frequent and troublesome symptom of Parkinson’s disease (PD). It can affect how medication is absorbed and impact daily life. Tune in to audio from this month’s Third Thursdays Webinar to hear our panel of experts discuss why constipation happens in Parkinson’s. They also cover managing and preventing constipation and the latest research on the gut-brain connection.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
Whether you have Parkinson’s or not, you can help move research forward. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
Mentioned in this episode:
Researchers are studying the link between sense of smell and brain health. People with and without Parkinson's can help by taking a scratch-and-sniff test. It’s free, mailed to your home and takes just 15 minutes to complete.mysmelltest.org/getstarted
Parkinson’s isn’t easy to diagnose — everyone’s symptoms differ based on their individual biology, leading to delays in diagnosis and treatment. One of The Michael J. Fox Foundation’s (MJFF) key areas of focus is finding ways to diagnose Parkinson’s disease earlier and more clearly, which could one day lead to more personalized treatments that can improve quality of life.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
There are so many ways to get involved in the research that is leading to clearer disease diagnosis. Learn more about your role in research at: https://www.michaeljfox.org/your-role-parkinsons-research
The Foundation’s landmark study, the Parkinson’s Precision Medicine Initiative, also known as PPMI, is recruiting volunteers. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi
Mentioned in this episode:
Researchers are studying the link between sense of smell and brain health. People with and without Parkinson's can help by taking a scratch-and-sniff test. It’s free, mailed to your home and takes just 15 minutes to complete.mysmelltest.org/getstarted
People living with Parkinson’s disease (PD) and their loved ones develop countless ways to adapt and make daily life easier as symptoms change. Members of The Michael J. Fox Foundation’s Patient Council and their care partners share decades of collective wisdom on living with PD. They came together for a live conversation at MJFF’s New York City offices to discuss what they’ve learned along their own disease journeys, from practical strategies and tools that make daily life easier to the mindsets and mantras that guide and sustain them. In this episode of the MJFF Parkinson’s Podcast, patient council member and guest host Larry Gifford, diagnosed with PD in 2017 and president of PD Avengers, together with his wife and care partner Rebecca, reflect on the advice given.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
The Foundation’s landmark study, the Parkinson’s Precision Medicine Initiative, also known as PPMI, is recruiting volunteers. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
Mentioned in this episode:
Researchers are studying the link between sense of smell and brain health. People with and without Parkinson's can help by taking a scratch-and-sniff test. It’s free, mailed to your home and takes just 15 minutes to complete.mysmelltest.org/getstarted
Many people diagnosed with Parkinson’s and their loved ones wonder what caused the disease. Researchers believe Parkinson’s is caused by a mix of genetic, environmental and age-related factors that may contribute differently to each person. Tune in to audio from this month’s Third Thursdays Webinar to hear our panel of leading Parkinson’s experts discuss the latest efforts to understand what causes the disease so we can better treat and one day prevent it altogether.
Join the movement to end Parkinson’s this Parkinson’s Awareness Month at michaeljfox.org/April
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
Whether you have Parkinson’s or not, you can help move research forward. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
Mentioned in this episode:
Researchers are studying the link between sense of smell and brain health. People with and without Parkinson's can help by taking a scratch-and-sniff test. It’s free, mailed to your home and takes just 15 minutes to complete.mysmelltest.org/getstarted
Parkinson’s disease (PD) is the world’s fastest-growing neurological disease, affecting millions globally. Yet many misconceptions persist about life with the disease, how to treat it and the research going into the search for better therapies. Tune into this episode of The Michael J. Fox Foundation’s Parkinson’s Podcast to listen to our panel of experts including people living with PD, a researcher and movement disorder specialists debunk common myths about Parkinson’s disease and answer community questions.
Discover opportunities to take action and join millions of others moving us closer to a cure. https://www.michaeljfox.org/parkinsons-awareness-month
Like our podcasts? Rate or review the show and share the series with your community. https://apple.co/3p02Jw0
The Foundation’s landmark study, the Parkinson’s Progression Markers Initiative, also known as PPMI, is recruiting volunteers. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
Mentioned in this episode:
Researchers are studying the link between sense of smell and brain health. People with and without Parkinson's can help by taking a scratch-and-sniff test. It’s free, mailed to your home and takes just 15 minutes to complete.mysmelltest.org/getstarted
Sleep is an important part of physical and mental health, but Parkinson’s symptoms and medication side effects can make a good night’s sleep hard to find. Insomnia, nocturia, medication wearing off, REM sleep behavior disorder (RBD) and more can interrupt sleep. Tune into audio from this month’s Third Thursdays Webinar to hear our panel of experts discuss the latest research on the connection between sleep and Parkinson’s disease (PD) and share practical strategies for setting yourself up for the best rest possible.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
Whether you have Parkinson’s or not, you can help move research forward. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi
Mentioned in this episode:
Researchers are studying the link between sense of smell and brain health. People with and without Parkinson's can help by taking a scratch-and-sniff test. It’s free, mailed to your home and takes just 15 minutes to complete.mysmelltest.org/getstarted
A world without Parkinson’s will only be made possible through the work and energy of the Parkinson’s community — people living with the disease and their loved ones, researchers, clinicians, industry leaders, lawmakers and others. Catalyzing that community towards productive action is one of The Michael J. Fox Foundation’s (MJFF) four main areas of research focus in its Strategic Research Agenda, along with more clearly defining Parkinson’s disease, building better treatment pipelines and speeding clinical trial decision-making.
In this episode of The Michael J. Fox Foundation Parkinson’s Podcast, part of its award-winning Parkinson’s Science POV series, Maggie Kuhl, vice president of patient engagement at MJFF, leads a conversation about these efforts with two veteran scientists: Brian Fiske, PhD, chief scientist, MJFF and Mark Frasier, PhD, chief scientist, MJFF.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
There are so many ways to get involved in Parkinson’s community, whether it’s becoming an advocate, joining Team Fox or participating in research. Learn more at michaeljfox.org
The Foundation’s landmark study, the Parkinson’s Progression Markers Initiative, also known as PPMI, is recruiting volunteers. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi
Mentioned in this episode:
Researchers are studying the link between sense of smell and brain health. People with and without Parkinson's can help by taking a scratch-and-sniff test. It’s free, mailed to your home and takes just 15 minutes to complete.mysmelltest.org/getstarted
How can I show up for my partner with Parkinson’s? How can I best support my parent with PD from afar? How can my loved one and I work together to make decisions as symptoms change?
Our community has many questions about how to best support a loved one with Parkinson’s disease. Tune in to audio from this month’s Third Thursdays Webinar to hear our panel of experts — including care partners, a person living with PD, a social worker and a psychologist — discuss strategies for effective communication and shared decision-making to keep a partnership strong through Parkinson’s.
This webinar received support from Acadia Pharmaceuticals. Learn more at: moretoparkinson’s.com
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
Whether you have Parkinson’s or not, you can help move research forward. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
Mentioned in this episode:
Researchers are studying the link between sense of smell and brain health. People with and without Parkinson's can help by taking a scratch-and-sniff test. It’s free, mailed to your home and takes just 15 minutes to complete.mysmelltest.org/getstarted
Diet is a useful tool to feel and live better, whether you live with Parkinson’s or not. But putting healthy eating into practice can be tricky. In audio from this popular Ask the MD video, movement disorder specialist, lifestyle medicine physician and MJFF Principal Medical Advisor Rachel Dolhun, DipABLM, speaks with Erin Presant, DO, movement disorder and culinary medicine specialist. Together, they answer common questions about how diet can support brain health and help manage disease.
Listen now or watch the video. You can also check out our page on lifestyle strategies for living well with Parkinson’s.
Rather listen on the go? Subscribe to our Michael J. Fox Foundation Parkinson’s Podcast wherever you get your podcasts.
Mentioned in this episode:
Researchers are studying the link between sense of smell and brain health. People with and without Parkinson's can help by taking a scratch-and-sniff test. It’s free, mailed to your home and takes just 15 minutes to complete.mysmelltest.org/getstarted
How does research into Parkinson’s and Alzheimer’s overlap, and what insights are being revealed? Tune into audio from this month’s Third Thursdays Webinar to hear our panel of experts discuss what scientists are learning about how these diseases affect the brain and how understanding their links may lead to better care for people living with a disease.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
Whether you have Parkinson’s or not, you can help move research forward. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi
Mentioned in this episode:
Researchers are studying the link between sense of smell and brain health. People with and without Parkinson's can help by taking a scratch-and-sniff test. It’s free, mailed to your home and takes just 15 minutes to complete.mysmelltest.org/getstarted
No matter your age, whether you have Parkinson’s or not, there are steps you can take today to boost your brain health. In this extended version of a popular Ask the MD video, movement disorder specialist, life medicine physician and MJFF Principal Medical Advisor Rachel Dolhun, MD, DipABLM, sits down with Ayesha Sherzai, MD, and Dean Sherzai, MD, PhD, known as The Brain Docs. Together they answer community questions and share tips for using lifestyle medicine to help your brain.
Mentioned in this episode:
Researchers are studying the link between sense of smell and brain health. People with and without Parkinson's can help by taking a scratch-and-sniff test. It’s free, mailed to your home and takes just 15 minutes to complete.mysmelltest.org/getstarted
Experiencing some stress is a normal part of life, but many people living with Parkinson’s notice stress may worsen symptoms and make medication less effective. And chronic stress can cause lasting impacts to mental and physical health. Tune into audio from this Third Thursday’s Webinar to hear our panel of experts discuss how stress affects the body and how to reduce its harm.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
Whether you have Parkinson’s or not, you can help move research forward. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi
Mentioned in this episode:
Researchers are studying the link between sense of smell and brain health. People with and without Parkinson's can help by taking a scratch-and-sniff test. It’s free, mailed to your home and takes just 15 minutes to complete.mysmelltest.org/getstarted
Earlier this year, The Michael J. Fox Foundation hosted its 2025 Research Roundtable, “Building on Breakthroughs.” Tune into audio from this event to hear Parkinson’s experts and MJFF staff discuss the latest in lifestyle medicine and treatments in the pipeline, as well as the power of advocating for Parkinson’s policy.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
Whether you have Parkinson’s or not, you can help move research forward. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi
Mentioned in this episode:
Researchers are studying the link between sense of smell and brain health. People with and without Parkinson's can help by taking a scratch-and-sniff test. It’s free, mailed to your home and takes just 15 minutes to complete.mysmelltest.org/getstarted
What is AI? How do scientists use it? Where does the data come from? Can AI help find a cure for Parkinson’s?
As the use of artificial intelligence, or AI, becomes more widespread, our community has asked us many questions about how scientists may be using the technology to further Parkinson’s research. In this episode of The Michael J. Fox Foundation Parkinson’s Podcast, in its award-wining "Parkinson’s Science POV" series, Maggie Kuhl, vice president of patient engagement at MJFF, leads a conversation to answer some of those questions with:
- Bradford Casey, PhD, senior scientific portfolio manager, MJFF
- Brian Fiske, PhD, chief scientist, MJFF
- Mark Frasier, PhD, chief scientist, MJFF
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
The Foundation’s landmark study, the Parkinson’s Progression Markers Initiative, also known as PPMI, is recruiting volunteers. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi
Mentioned in this episode:
Researchers are studying the link between sense of smell and brain health. People with and without Parkinson's can help by taking a scratch-and-sniff test. It’s free, mailed to your home and takes just 15 minutes to complete.mysmelltest.org/getstarted
Parkinson’s research has had a transformative year as researchers have built on breakthroughs to learn more about the disease and how to treat it. Tune into audio from this Third Thursday’s Webinar to hear our panel of experts discuss how Parkinson’s research has advanced in 2025 and what the future could look like.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
Whether you have Parkinson’s or not, you can help move research forward. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi
Read more about this year in research at https://viewer.joomag.com/2025-year-in-review/0030141001760361264
Mentioned in this episode:
From now through December 2, you can help accelerate Parkinson’s research. This Giving Tuesday, all donations to The Michael J. Fox Foundation will be matched up to $4 million, which means your impact will be doubled. Visit michaeljfox.org/givetoresearch to be part of the cure.
As Parkinson’s symptoms change over the years, different treatments may be needed to best manage symptoms and side effects. Since last fall, the U.S. Food and Drug Administration has approved five new options for people living with the disease, including two continuous, under-the-skin infusion pumps. Tune into audio from this Third Thursday’s Webinar to hear our panel of experts discuss these options and other strategies to treat progressing Parkinson’s disease.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
Whether you have Parkinson’s or not, you can help move research forward. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
Mentioned in this episode:
The Foundation’s landmark research study is exploring the connection between sense of smell and brain disease. People with and without Parkinson's can help by taking a free scratch-and-sniff test. Get yours at mysmelltest.org/request.
Stepping back from the workforce is a milestone event in any life, and Parkinson’s disease (PD) adds an emotional and logistical layer. Many people living with the disease think differently about when and how to retire as they balance symptoms, their financial and health needs and their plans and interests. Tune into this episode of The Michael J. Fox Foundation’s Parkinson’s Podcast to listen to our expert panel of a person living with Parkinson’s, a care partner and people who work with the Parkinson’s community discuss retirement and Parkinson’s. They share advice from their own lives and tips for people entering a new phase of their life.
Check out our free employment guide. https://www.michaeljfox.org/news/workplace-challenges
Like our podcasts? Rate or review the show and share the series with your community. https://apple.co/3p02Jw0
The Foundation’s landmark study, the Parkinson’s Progression Markers Initiative, also known as PPMI, is recruiting volunteers. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi
Mentioned in this episode:
The Foundation’s landmark research study is exploring the connection between sense of smell and brain disease. People with and without Parkinson's can help by taking a free scratch-and-sniff test. Get yours at mysmelltest.org/request.
While there have been improvements in therapies to treat Parkinson’s symptoms, people living with the disease and their loved ones await a treatment that will slow the progression of Parkinson’s disease (PD) or stop it entirely. These therapies, called disease-modifying therapies, have the potential to change how PD is treated and experienced. Tune into audio from this Third Thursdays Webinar to listen to our panel of experts discuss disease-modifying therapies and the latest in Parkinson’s research.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
Whether you have Parkinson’s or not, you can help move research forward. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
This webinar was produced with support from Biohaven. https://www.biohavenclinicaltrials.com/clinical-studies/parkinsons-disease/
Mentioned in this episode:
The Foundation’s landmark research study is exploring the connection between sense of smell and brain disease. People with and without Parkinson's can help by taking a free scratch-and-sniff test. Get yours at mysmelltest.org/request.
A Parkinson’s disease (PD) diagnosis can impact many areas of life, including how you get work done and think about your career. It can lead to questions like: Should I disclose my diagnosis to my employer and colleagues? How do I adapt my work around my symptoms? What legal protections do I have? Tune into this episode of The Michael J. Fox Foundation’s Parkinson’s Podcast to listen to our expert panel of people living with PD, a care partner, and an employment consultant discuss employment and Parkinson’s. They share their stories and offer the tips they’ve learned along the way.
Check out our free employment guide. https://www.michaeljfox.org/news/workplace-challenges
Like our podcasts? Rate or review the show and share the series with your community. https://apple.co/3p02Jw0
The Foundation’s landmark study, the Parkinson’s Progression Markers Initiative, also known as PPMI, is recruiting volunteers. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
Mentioned in this episode:
The Foundation’s landmark research study is exploring the connection between sense of smell and brain disease. People with and without Parkinson's can help by taking a free scratch-and-sniff test. Get yours at mysmelltest.org/request.
Researchers are investigating many options to treat Parkinson’s disease (PD) with stem cells, including reprogramming them to replace lost dopamine-producing neurons and creating supportive brain cells to keep neurons healthy. Tune into audio from this Third Thursdays Webinar to listen to our panel of experts discuss the latest stem cell research and answer audience questions.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
Whether you have Parkinson’s or not, you can help move research forward. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
This webinar was produced with support from BlueRock Therapeutics.
Mentioned in this episode:
The Foundation’s landmark research study is exploring the connection between sense of smell and brain disease. People with and without Parkinson's can help by taking a free scratch-and-sniff test. Get yours at mysmelltest.org/request.
How do I tell my children about my Parkinson’s disease (PD) diagnosis? How do I explain a tremor to my grandkids? How can I support my parent with Parkinson’s from a distance? How can my spouse and I communicate around a symptom of apathy?
Every year our community submits thousands of questions online and at in-person events. Many are about Parkinson’s symptoms, treatment options and the latest research, but we’re also asked questions about relationships and how to maintain connection with loved ones with Parkinson’s in the picture. In this episode of The Michael J. Fox Foundation’s Parkinson’s Podcast, our expert panel tackles questions on relationships and shares their personal experiences and advice.
To connect with others for support and community, join the Parkinson’s Buddy Network. https://parkinsonsbuddynetwork.michaeljfox.org/
Like our podcasts? Rate or review the show and share the series with your community. https://apple.co/3p02Jw0
The Foundation’s landmark study, the Parkinson’s Progression Markers Initiative, also known as PPMI, is recruiting volunteers. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi
Mentioned in this episode:
The Foundation’s landmark research study is exploring the connection between sense of smell and brain disease. People with and without Parkinson's can help by taking a free scratch-and-sniff test. Get yours at mysmelltest.org/request.
Technology can offer people living with Parkinson’s disease (PD) much needed support in several areas of life, from apps to keep track of medication timing, wearables to help smooth gait, websites to monitor symptoms and more. Tune into audio from this Third Thursdays Webinar to listen to our panel of experts discuss how tech tools can be incorporated in daily living with PD and how to find your best options. They also share personal tips and experiences and answer audience questions.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
Whether you have Parkinson’s or not, you can help move research forward. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi
Mentioned in this episode:
The Foundation’s landmark research study is exploring the connection between sense of smell and brain disease. People with and without Parkinson's can help by taking a free scratch-and-sniff test. Get yours at mysmelltest.org/request.
Advances in imaging technology offer researchers a window into how Parkinson’s disease affects the brain, which could reshape how the disease is diagnosed and treated. In this episode of The Michael J. Fox Foundation Parkinson’s Podcast, in its award-winning Parkinson’s Science POV series, David Kumbroch, senior science writer at MJFF, lead a conversation with:
- Jamie Eberling, PhD, senior vice present of research resources at MJFF.
- Roger Gunn, PhD, chief science officer at Xing Imaging.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
Learn more about the many ways to get involved today at michaeljfox.org
Whether you have Parkinson’s or not, you can help move research forward. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi
Mentioned in this episode:
The Foundation’s landmark research study is exploring the connection between sense of smell and brain disease. People with and without Parkinson's can help by taking a free scratch-and-sniff test. Get yours at mysmelltest.org/request.
Having a network of health care professionals, loved ones and community members as part of a care team has shown to improve the quality of life for those living with Parkinson’s disease (PD) and their loved ones. Tune into audio from this Third Thursdays Webinar to listen to our panel of experts discuss how to make the most of your appointments, find specialists and coordinate care to best support the person living with the disease.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
Whether you have Parkinson’s or not, you can help move research forward. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi
Mentioned in this episode:
The Foundation’s landmark research study is exploring the connection between sense of smell and brain disease. People with and without Parkinson's can help by taking a free scratch-and-sniff test. Get yours at mysmelltest.org/request.
Life with Parkinson’s disease (PD) is shaped by myriad factors, including sexual orientation and gender identity that shape access to care, lifestyle decisions and more. In this episode of The Michael J. Fox Foundation’s Parkinson’s Podcast, our expert panel shares their personal stories and discusses the ongoing research into the health concerns and needs of LGBTQ+ people living with PD.
To connect with others for support and community, join the Parkinson’s Buddy Network. https://parkinsonsbuddynetwork.michaeljfox.org/
Like our podcasts? Rate or review the show and share the series with your community. https://apple.co/3p02Jw0
The Foundation’s landmark study, the Parkinson’s Progression Markers Initiative, also known as PPMI, is recruiting volunteers. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
Mentioned in this episode:
The Foundation’s landmark research study is exploring the connection between sense of smell and brain disease. People with and without Parkinson's can help by taking a free scratch-and-sniff test. Get yours at mysmelltest.org/request.
The beliefs and perceptions that friends, family, employers and even strangers hold about Parkinson’s disease (PD) shape the experience of living with the disease. Facing misperceptions and stigma can cause isolation and worsen symptoms. Tune into audio from this Third Thursdays Webinar to listen to our panel of experts have a candid and compassionate conversation about times they’ve faced stigma, how they’ve navigated it and how they’re working to change misperceptions of Parkinson’s to improve life for everyone living with the disease.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
Whether you have Parkinson’s or not, you can help move research forward. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
Mentioned in this episode:
The Foundation’s landmark research study is exploring the connection between sense of smell and brain disease. People with and without Parkinson's can help by taking a free scratch-and-sniff test. Get yours at mysmelltest.org/request.
There are so many ways to get involved with Parkinson’s disease, from community building to advocacy, research participation to fundraising. Taking that first step toward involvement can be daunting, but many people say it’s a critical part of living well with the disease. In this episode of The Michael J. Fox Foundation Parkinson’s Podcast, members of the Foundation’s Patient Council share stories of their own first steps, explore how engagement has impacted their journeys and offer advice and perspective to others who are looking for ways to make meaningful change. Tune in to hear guest hosts Jimmy Choi, diagnosed with Parkinson’s in 2003, and Hadley Ferguson, diagnosed with multiple system atrophy (MSA-P), an atypical Parkinsonism in 2014, reflect on those stories, recorded live in the MJFF offices.
Learn more about the many ways to get involved today at michaeljfox.org.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
The Foundation’s landmark study, the Parkinson’s Progression Marker’s Initiative, also known as PPMI, is recruiting volunteers. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
Mentioned in this episode:
The Foundation’s landmark research study is exploring the connection between sense of smell and brain disease. People with and without Parkinson's can help by taking a free scratch-and-sniff test. Get yours at mysmelltest.org/request.
Life with Parkinson’s comes with a vast range of emotions, wherever you are in your disease journey. Shock, grief, optimism, fear, denial, hope, humor and more can all be a part of the emotional landscape for people living with the disease and their loved ones. Tune into audio from this special edition Third Thursdays Webinar to listen to our panel of experts have a frank and deep conversation about how they’ve navigated their feelings over the years, how they’ve managed challenging emotions and what lifts them up and brings them hope.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
The Foundation’s landmark study, the Parkinson’s Progression Marker’s Initiative, also known as PPMI, is recruiting volunteers. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
Mentioned in this episode:
The Foundation’s landmark research study is exploring the connection between sense of smell and brain disease. People with and without Parkinson's can help by taking a free scratch-and-sniff test. Get yours at mysmelltest.org/request.
Smell loss can be among the earliest signs of Parkinson’s disease (PD) and other neurodegenerative diseases, signaling changes in the brain years before other symptoms are noticeable. Because of the link between smell and brain health, researchers are very interested in understanding more about how people with smell loss go on to either develop a disease or not, and why some people with PD still are able to smell. To learn more about the latest research, tune into audio from this Third Thursdays Webinar and listen to expert panelists discuss the science of smell and what scientists are learning about its connection to disease.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
The Foundation’s landmark study, the Parkinson’s Progression Marker’s Initiative, also known as PPMI, is recruiting volunteers. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
Mentioned in this episode:
The Foundation’s landmark research study is exploring the connection between sense of smell and brain disease. People with and without Parkinson's can help by taking a free scratch-and-sniff test. Get yours at mysmelltest.org/request.
You could take any two humans on earth and their genetic code will be roughly 99 percent the same — it’s the small differences in code that lead to different experiences and outcomes, including the risk of developing diseases like Parkinson’s. Scientists are learning more about which genetic changes are linked to Parkinson’s disease, revealing important insights into disease biology and progression. Tune into this episode of our award-winning “Parkinson’s Science POV” series to learn how researchers are using genetics to better understand the disease and work toward better treatments for all.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
The Foundation’s landmark study, the Parkinson’s Progression Marker’s Initiative, also known as PPMI, is recruiting volunteers. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
This episode was made possible by Prevail Therapeutics. Partner support allows us to furnish high-quality educational content to the Parkinson's community while maintaining our commitment to allocate donor dollars to high-impact research. Editorial control of all Michael J. Fox Foundation-published content rests solely with the Foundation.
Mentioned in this episode:
The Foundation’s landmark research study is exploring the connection between sense of smell and brain disease. People with and without Parkinson's can help by taking a free scratch-and-sniff test. Get yours at mysmelltest.org/request.
With three new Parkinson’s treatments approved in the last year, there are more options than ever before for people living with the disease. Tune into audio from this Third Thursdays Webinar to hear movement disorder specialists, research experts and a person living with Parkinson’s answer community questions about the new treatments available, explain how therapies make it through FDA approval and share the latest on treatments in the pipeline.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
The Foundation’s landmark study, the Parkinson’s Progression Marker’s Initiative, also known as PPMI, is recruiting volunteers. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
Mentioned in this episode:
The Foundation’s landmark research study is exploring the connection between sense of smell and brain disease. People with and without Parkinson's can help by taking a free scratch-and-sniff test. Get yours at mysmelltest.org/request.
Movement disorder specialist, lifestyle medicine physician and MJFF Principal Medical Advisor Rachel Dolhun, MD, DipABLM, shares tips on medication management for people at every stage of the disease journey.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
The Foundation’s landmark study, the Parkinson’s Progression Marker’s Initiative, also known as PPMI, is recruiting volunteers. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
Mentioned in this episode:
The Foundation’s landmark research study is exploring the connection between sense of smell and brain disease. People with and without Parkinson's can help by taking a free scratch-and-sniff test. Get yours at mysmelltest.org/request.
If depression, anxiety or apathy occur as part of a Parkinson’s journey, it can be easy to feel alone, isolated or unsure of what might bring relief. But there are ways to manage these symptoms. Tune into audio from this Third Thursdays Webinar to hear people living with Parkinson’s share their stories of coping with mood changes as well as a movement disorder specialist and psychiatrist discuss pharmacological and non-pharmacological treatments options.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
The Foundation’s landmark study, the Parkinson’s Progression Marker’s Initiative, also known as PPMI, is recruiting volunteers. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
Mentioned in this episode:
The Foundation’s landmark research study is exploring the connection between sense of smell and brain disease. People with and without Parkinson's can help by taking a free scratch-and-sniff test. Get yours at mysmelltest.org/request.
Movement disorder specialist, lifestyle medicine physician and MJFF Principal Medical Advisor Rachel Dolhun, MD, DipABLM, answers community questions on Parkinson’s and exercise with physical therapist and rehab scientist Cristina Colón-Semenza, PhD.
Listen to the audio or watch the video.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
The Foundation’s landmark study, the Parkinson’s Progression Marker’s Initiative, also known as PPMI, is recruiting volunteers. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
Mentioned in this episode:
The Foundation’s landmark research study is exploring the connection between sense of smell and brain disease. People with and without Parkinson's can help by taking a free scratch-and-sniff test. Get yours at mysmelltest.org/request.
Being a care partner to someone with Parkinson’s disease (PD) can be a shifting and complex role, as symptoms and life circumstances change. And sometimes, this can lead to stress and even burnout for the care partner. Tune into audio from this Third Thursdays Webinar to hear expert panelists discuss how to navigate care partnership, including everyday strategies to de-stress and find supportive community.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
The Foundation’s landmark study, the Parkinson’s Progression Marker’s Initiative, also known as PPMI, is recruiting volunteers. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
Mentioned in this episode:
The Foundation’s landmark research study is exploring the connection between sense of smell and brain disease. People with and without Parkinson's can help by taking a free scratch-and-sniff test. Get yours at mysmelltest.org/request.
It is widely known that a healthy diet can provide essential nutrients and lead to a multitude of benefits, but growing evidence has highlighted important links between diet, nutrition, and brain health, particularly related to neurodegenerative disease. In this episode, Dr. Puja Agarwal discusses her research investigating the role that diet and nutrition may play in Parkinson’s disease and other neurodegenerative conditions. Evidence from her studies and the work of others suggests that certain diets, including the Mediterranean-DASH Intervention for Neurodegenerative Delay (MIND) diet, are associated with brain health and may have the potential to delay the onset or slow progression of Parkinson's disease or other neurodegenerative conditions. We hear more about her ongoing MJFF-funded research project examining the role of diet in the progression of parkinsonian signs and its association with Lewy body pathologies, as well as future directions for this exciting line of research. Puja is an Assistant Professor in the Department of Internal Medicine at Rush University.
Mentioned in this episode:
The Foundation’s landmark research study is exploring the connection between sense of smell and brain disease. People with and without Parkinson's can help by taking a free scratch-and-sniff test. Get yours at mysmelltest.org/request.
This podcast episode was part of a limited series created by The Michael J. Fox Foundation in 2023 and 2024 for clinicians and researchers in our audience. These episodes provide a deeper dive into exciting new scientific research in Parkinson’s disease, as well as innovative tools and valuable resources, through conversations with a variety of experts in the field. We hope you enjoy the conversation.
Parkinson's disease significantly impacts various aspects of communication, and this can make it challenging for people with the disease to communicate effectively, be understood by others, and engage in social situations. Dr. Gemma Moya-Galé joins this episode to talk about her work on voice and communication in people with Parkinson’s disease. In particular, she discusses a novel app she and her team are developing, with funding from The Michael J. Fox Foundation, to help people with Parkinson’s improve how well their speech is understood. The app uses evidence-based principles from speech therapy and noise-augmented automatic speech recognition to provide speech training and feedback. She also shares her recent research on linguistically and culturally responsive methods for addressing communication challenges in both English- and Spanish-speaking individuals with Parkinson's disease, and how this approach has the potential to improve clinical care. Gemma is an Assistant Professor of Communication Sciences and Disorders, as well as the Director of the Communication, Technology, and Language Diversity Lab at Teachers College, Columbia University.
Mentioned in this episode:
The Foundation’s landmark research study is exploring the connection between sense of smell and brain disease. People with and without Parkinson's can help by taking a free scratch-and-sniff test. Get yours at mysmelltest.org/request.
This podcast episode was part of a limited series created by The Michael J. Fox Foundation in 2023 and 2024 for clinicians and researchers in our audience. These episodes provide a deeper dive into exciting new scientific research in Parkinson’s disease, as well as innovative tools and valuable resources, through conversations with a variety of experts in the field. We hope you enjoy the conversation.
Understanding the biology of Parkinson’s disease (PD) and turning that knowledge into better treatments is a complex undertaking. In this episode of the award-winning Parkinson’s Science POV series, scientists at The Michael J. Fox Foundation (MJFF) discuss how they are tackling this problem from every angle. Whether it’s using cutting-edge imaging to get a picture of the disease in the brain or working with the community to develop better options to treat walking difficulties, our researchers are collaborating to discover the next wave of treatment options and close in on a cure.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
Watch our webinar or read our Year in Review at michaeljfox.org.
The Foundation’s landmark study, the Parkinson’s Progression Marker’s Initiative, also known as PPMI, is recruiting volunteers. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
Mentioned in this episode:
The Foundation’s landmark research study is exploring the connection between sense of smell and brain disease. People with and without Parkinson's can help by taking a free scratch-and-sniff test. Get yours at mysmelltest.org/request.
Certain populations are disproportionately affected by neurological diseases, including Parkinson's and other neurodegenerative diseases. A lot of work remains to be done to improve brain health outcomes and promote healthy brain aging across the lifespan, particularly for minoritized, underrepresented populations. Including participants from diverse backgrounds in research helps ensure that the results from studies and clinical trials in the field are valid, generalizable, and representative of all individuals affected by these diseases.
In this episode, Dr. Monica Rivera-Mindt discusses brain health inequities in neurodegenerative diseases, her work using culturally informed community-engaged research methods to improve representation in research studies, important gaps in the literature, lessons learned from the Alzheimer's Disease Neuroimaging Initiative (ADNI) Diversity Task Force that could be applied in Parkinson's disease research, and more. Monica is Professor of Psychology, Latinx studies, and African and African American studies at Fordham University, and she has a joint appointment as Professor of Neurology at the Icahn School of Medicine at Mount Sinai. She is also a board-certified neuropsychologist.
Mentioned in this episode:
This podcast episode was part of a limited series created by The Michael J. Fox Foundation in 2023 and 2024 for clinicians and researchers in our audience. These episodes provide a deeper dive into exciting new scientific research in Parkinson’s disease, as well as innovative tools and valuable resources, through conversations with a variety of experts in the field. We hope you enjoy the conversation.
The Foundation’s landmark research study is exploring the connection between sense of smell and brain disease. People with and without Parkinson's can help by taking a free scratch-and-sniff test. Get yours at mysmelltest.org/request.
With two new drugs approved by the FDA, a National Plan signed into law and many advances in our understanding of Parkinson’s disease, 2024 has been a transformative year in Parkinson’s research. Tune into audio from this month’s Third Thursdays Webinar to hear research experts from industry and academia talk with MJFF staff about the latest research on disease biology and emerging therapies.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
The Foundation’s landmark study, the Parkinson’s Progression Marker’s Initiative, also known as PPMI, is recruiting volunteers. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
Mentioned in this episode:
The Foundation’s landmark research study is exploring the connection between sense of smell and brain disease. People with and without Parkinson's can help by taking a free scratch-and-sniff test. Get yours at mysmelltest.org/request.
Alpha-synuclein plays a key role in the pathophysiology of Parkinson's disease, and researchers have been investigating this protein as a therapeutic target and also as a potential biomarker for the disease. The alpha-synuclein seed amplification assay, developed by Dr. Claudio Soto and colleagues, leverages the self-replicating nature of the misfolded alpha-synuclein proteins that form aggregates in Parkinson's disease. Amplifying misfolded alpha-synuclein can allow researchers and clinicians to detect the presence of the pathological form of the protein in biospecimens, even when the amount of misfolded alpha-synuclein in a sample is very low. In this episode, Claudio discusses his work in this area and how it has opened the doors for a variety of potential uses of the alpha-synuclein seed amplification assay, including applications in diagnosis, clinical trials, and drug development for Parkinson's disease.
This year, Claudio received the 2024 Robert A. Pritzker Prize for Leadership in Parkinson’s Research for his substantial contributions to research and his commitment to mentoring the next generation of scientists in the field. Claudio is the Huffington’s Distinguished University Chair, Professor of Neurology, and Director of the George and Cynthia Mitchell Center for Alzheimer’s Disease and Related Brain Disorders at The University of Texas Medical School in Houston. He is also the Founder, Vice-President, and Chief Scientific Officer at AMPRION Inc.
Mentioned in this episode:
The Foundation’s landmark research study is exploring the connection between sense of smell and brain disease. People with and without Parkinson's can help by taking a free scratch-and-sniff test. Get yours at mysmelltest.org/request.
This podcast episode was part of a limited series created by The Michael J. Fox Foundation in 2023 and 2024 for clinicians and researchers in our audience. These episodes provide a deeper dive into exciting new scientific research in Parkinson’s disease, as well as innovative tools and valuable resources, through conversations with a variety of experts in the field. We hope you enjoy the conversation.
Each person living with Parkinson’s disease (PD) will have a unique journey with their treatments, including the decision to have deep brain stimulation (DBS), which is a surgical procedure to treat Parkinson’s motor symptoms. While DBS isn’t suitable for everyone, it can be helpful in the right person, and it’s a complex, lifelong choice. And although the experience goes far beyond surgery day, brain surgery often looms large in people’s minds as they are contemplating DBS. In this episode, our expert panelists tackle community-sourced questions on DBS surgery day: what to wear, how loved ones can support, what it feels like to be awake during brain surgery and more. Tune in to hear from two people who have had DBS, a neurosurgeon and a movement disorder specialist and learn more about the realities of surgery day.
For more information on deep brain stimulation, download our newly updated, comprehensive guide or check out our webinar at michaeljfox.org.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community: https://apple.co/3p02Jw0
The Foundation’s landmark study, the Parkinson’s Progression Marker’s Initiative, also known as PPMI, is recruiting volunteers. People from all backgrounds with and without Parkinson’s can help move research forward. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
Mentioned in this episode:
This Giving Tuesday, December 3, you can help us sustain and grow the momentum in Parkinson’s research. All donations will be matched up to $4 million, which means your impact will be doubled. Visit michaeljfox.org/match2024 to help us accelerate research and be part of the cure.
Troubles with gait – slow walking, shuffling steps and foot dragging and more – can be symptoms of Parkinson’s. In audio from this Third Thursdays Webinar, our experts explore the robust research efforts underway to understand and treat gait issues, from physical rehab interventions to deep brain stimulation modifications to wearable robots designed to smooth gait.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
The Foundation’s landmark study, the Parkinson’s Progression Marker’s Initiative, also known as PPMI, is recruiting volunteers. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
Mentioned in this episode:
This Giving Tuesday, December 3, you can help us sustain and grow the momentum in Parkinson’s research. All donations will be matched up to $4 million, which means your impact will be doubled. Visit michaeljfox.org/match2024 to help us accelerate research and be part of the cure.
In this podcast, four people from different backgrounds have a candid conversation on race, stigma and Parkinson’s. They share their experiences trying to find culturally competent medical professionals, overcoming the barriers to research participation, and communicating with their communities about their diagnosis. And they offer tips and advice on finding empowerment through education and advocacy.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community: https://apple.co/3p02Jw0
The Foundation’s landmark study, the Parkinson’s Progression Marker’s Initiative, also known as PPMI, is recruiting volunteers. People from all backgrounds with and without Parkinson's can help move research forward. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
Mentioned in this episode:
This Giving Tuesday, December 3, you can help us sustain and grow the momentum in Parkinson’s research. All donations will be matched up to $4 million, which means your impact will be doubled. Visit michaeljfox.org/match2024 to help us accelerate research and be part of the cure.
Parkinson’s disease brings with it many potential symptoms, including hallucinations (seeing things that are not there) and delusions (believing things that are not true). Not everyone will experience these symptoms and not everyone who does will find them bothersome, but it can be a source of uncertainty and concern for people living with the disease. In audio from this Third Thursdays Webinar, our expert panel discusses navigating life with these symptoms and medication and non-medication strategies to manage them.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
The Foundation’s landmark study, the Parkinson’s Progression Marker’s Initiative, also known as PPMI, is recruiting volunteers. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
Mentioned in this episode:
Our landmark study is examining the link between smell loss and risk for Parkinson’s disease in people of all backgrounds. If you’re age 60 or older and do not have Parkinson’s, you can help move this research forward by taking a free scratch-and-sniff test. Get yours today at mysmelltest.org/request.
Finding the right Parkinson’s treatment plan can be a trial-and-error process. The kind of medication, the dosage, the timing and lifestyle factors are all important pieces of the puzzle. In audio from this Third Thursdays Webinar, our expert panel made up of people living with Parkinson’s disease (PD), a movement disorder specialist and a researcher discuss different medication options, practical tips for finding what works best for you and the latest research on emerging treatments.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
The Foundation’s landmark study, the Parkinson’s Progression Markers Initiative, also known as PPMI, is recruiting volunteers. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
Research shows mindfulness and meditation can improve some Parkinson’s (PD) symptoms and live a better life with the disease, but it can be tricky to put into practice. In this podcast, you’ll hear from people whose lives have been touched by PD and who use mindfulness to reduce symptoms and stress, and from a researcher who is studying how mind-body strategies can be used to treat Parkinson’s. Tune in for practical tips, advice and a guided meditation you can try at home.
You can find links to the resources mentioned in the episode on our website: https://www.michaeljfox.org/podcast/breathing-through-mindfulness-parkinsons-treatment-tool
You can also download our free guide on exercise and Parkinson’s disease, which includes tips for incorporating meditation into your daily routine at michaeljfox.org/exerciseguide
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
Mentioned in this episode:
Make-A-Will Month
August is Make-A-Will Month, which serves as a reminder of the importance of creating and updating your will. Use this moment to take control of your future and ensure your wishes are respected. Visit michaeljfox.org/plan to learn more and get started.
The decision-making process around deep brain stimulation (DBS) to treat Parkinson’s motor symptoms can be a complex and emotional journey. People often have questions about when – and whether – to have the procedure and what the experience is like, from the months of evaluation pre-surgery to surgery day to life with the device. In audio from this Third Thursdays Webinar, our panel of people living with Parkinson’s disease (PD) and a movement disorder specialist share their DBS stories and answer audience questions about their choices and experiences.
Learn more about deep brain stimulation and download our free guide on our website: https://bit.ly/4cTOT52
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community.
The Foundation’s landmark study, the Parkinson’s Progression Markers Initiative, also known as PPMI, is recruiting volunteers. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
Just over a year ago, there was a major breakthrough in Parkinson’s disease (PD) research – a tool that could detect abnormal alpha-synuclein protein in the spinal fluid of people living with PD even before onset of symptoms. This discovery is already impacting the ways scientists conduct and think about Parkinson’s research. Tune into this episode of our award-winning “Parkinson’s Science POV” series to learn how researchers are using the test to better understand disease biology and what the future holds.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
The Foundation’s landmark study, the Parkinson’s Progression Markers Initiative, also known as PPMI, is recruiting volunteers. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
You might be interested in stepping forward for science to play a role in the next breakthrough in Parkinson’s research, but still have questions about how to actually participate. How do you pick the right study for you? How do you balance your life logistics and your medical care considerations? What rights do you have when you participate in a study? In audio from this Third Thursdays Webinar, our panel of people living with Parkinson’s and research experts discuss the practicalities and benefits of volunteering for research.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
The Foundation’s landmark study, the Parkinson’s Progression Markers Initiative, also known as PPMI, is recruiting volunteers. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
Many people living with Parkinson’s disease (PD) experience pain as a non-motor symptom. Pain can arise from stiff muscles, dystonia, nerve pain and even the disease progression itself. It’s a symptom that some find difficult to talk about, but there are options for people to find relief. In audio from this Third Thursdays webinar, listen to our expert panel of people living with PD, movement disorder specialists, and an integrative pain specialist discuss pain and Parkinson’s – why it happens, treatments to reduce it, and practical tips you can start incorporating today.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0
The Foundation’s landmark study, the Parkinson’s Progression Markers Initiative, also known as PPMI, is recruiting volunteers. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
In this episode, hosted by Larry and Rebecca Gifford, members of The Michael J. Fox Foundation’s Patient Council and their care partners share their honest reactions to their diagnosis — from panic and denial to sadness and loneliness. This group of men and women of different ages and backgrounds offers words of wisdom about what to consider, what they’ve lost and what they’ve gained – and you’ll be surprised to hear how, for some, what they’ve gained is more than what they lost.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. https://apple.co/3p02Jw0
If you or a loved one was recently diagnosed and you’re wondering where to start, visit https://www.michaeljfox.org/newlydiagnosed to find helpful resources, including an educational guide, support groups and videos.
Whether you’ve been newly diagnosed or have been living with Parkinson’s for many years, The Michael J. Fox Foundation’s Parkinson’s Buddy Network is a free, online platform that helps you find new connections, access educational resources and engage in important dialogue. Join our community today at parkinsonsbuddynetwork.org.
The Foundation’s landmark study, the Parkinson’s Progression Markers Initiative, also known as PPMI, is recruiting volunteers. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
In this raw and emotional conversation, four women with Parkinson’s living in four different countries discuss the challenges faced because of delayed diagnosis, hormonal changes, lack of information and treatment, research inequity and gender biases. They share how they live better with the disease by advocating for themselves with their health care team and how they empower other women through awareness and activism.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. https://apple.co/3p02Jw0
Connect with other women who share your experiences with Parkinson’s. The Michael J. Fox Foundation’s Parkinson’s Buddy Network is a free, online platform that helps you find new connections, access educational resources and engage in important dialogue. Join our community today at parkinsonsbuddynetwork.org.
The Foundation’s landmark study, the Parkinson’s Progression Markers Initiative, also known as PPMI, is recruiting volunteers. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
Living with Parkinson’s comes with a variety of symptoms, some of which can be unexpected, and frankly, embarrassing. Drooling, bladder issues and sexual dysfunction are hard to talk about, even with loved ones or your doctor – and can affect your self-image, your intimate relationships or the way you move through the world. In audio from this Third Thursdays webinar, listen to our expert panel of people living with Parkinson’s, a care partner and a movement disorder specialist discuss Parkinson’s taboo topics and ways that you can navigate hard conversations and embarrassment.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. https://apple.co/3p02Jw0
Whether you’ve been newly diagnosed or have been living with Parkinson’s for many years, The Michael J. Fox Foundation’s Parkinson’s Buddy Network is a free, online platform that helps you find new connections, access educational resources and engage in important dialogue. Join our community today at parkinsonsbuddynetwork.org.
The Foundation’s landmark study, the Parkinson’s Progression Markers Initiative, also known as PPMI, is recruiting volunteers. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
The biology behind what causes Parkinson’s is complex, with only about a quarter of cases with clear genetic drivers. The environment – where you live, the air you breathe, the food you eat, the world around you – plays a key role in PD. Emerging research is showing environmental exposures to things like pesticides and pollution may interact with a person’s genetics and contribute to the disease. And there’s a myriad of other factors still being investigated, from the forces that drive your access to neighborhoods with clean air and water, good doctors and healthy living opportunities to psychosocial factors like stress and discrimination. In audio from this Third Thursdays Webinar, listen to our expert panel discuss the latest research and ways you can get involved to end preventable exposures and advocate for Parkinson’s policy.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. https://apple.co/3p02Jw0
The Foundation’s landmark study, the Parkinson’s Progression Markers Initiative, also known as PPMI, is recruiting volunteers. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
The drug development pipeline is key to bringing new therapies to people with Parkinson’s disease (PD). With major breakthroughs in research in the past year, including a new biomarker for PD, The Michael J. Fox Foundation’s Parkinson’s Progression Markers Initiative (PPMI) study and other initiatives can be leveraged to create better designed trials. This audio from our Third Thursdays Webinar features a conversation about all the ways clinical trial design is changing, and why leaders in the space believe those changes will lead to better treatments. The webinar includes contributions from a person with PD, a researcher and an industry leader.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. https://apple.co/3p02Jw0
Whether you have Parkinson’s or not, you can help move research forward. Join the study that’s changing everything. Find out more at michaeljfox.org/podcast-ppmi.
Dating and beginning new relationships with Parkinson’s involve distinct challenges, joys and fears. In this frank and funny podcast, our experts discuss how they face considerations like building and maintaining confidence, disease disclosure, and the importance of self-knowledge and self-care in new relationships. They remind us all that no matter what we’re facing, dating and finding love can be fun and fulfilling.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. https://apple.co/3p02Jw0
Whether you’ve been newly diagnosed or have been living with Parkinson’s for many years, The Michael J. Fox Foundation’s Parkinson’s Buddy Network is a free, online platform that helps you find new connections, access educational resources and engage in important dialogue. Join our community today at parkinsonsbuddynetwork.org.
The Foundation’s landmark study, the Parkinson’s Progression Markers Initiative, also known as PPMI, is recruiting volunteers. Join the study that’s changing everything at michaeljfox.org/podcast-ppmi.
We know exercise is important for people with Parkinson’s. Once you’ve decided to move more, what next? In this audio from our Third Thursdays Webinar, our experts discuss strategies for making exercise a meaningful part of your life. They present ways to make time for exercise and to make the most of it, including being aware of different types, frequencies and intensities. This discussion will help you find a way to get moving and stay motivated.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. https://apple.co/3p02Jw0
Join a Foundation-hosted run/walk event. Or register for the Unity Walk. Every mile moves us one step closer to a cure for Parkinson's. Learn more at michaeljfox.org.
Whether you have Parkinson’s or not, you can help move research forward. Join the study that’s changing everything. Find out more at michaeljfox.org/podcast-ppmi.
One key pillar of The Michael J. Fox Foundation’s research strategy is a focus on “de-risking" potential treatments for Parkinson’s disease. This episode of our award-winning “Parkinson’s Science POV” series explains how lowering the risk associated with developing new therapies leads to a more robust pipeline of treatments. The episode details several recent successes of the strategy.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. https://apple.co/3p02Jw0
Join a study today to help speed progress toward better treatments and a cure for Parkinson’s disease. To search for studies in your area, visit Fox Trial Finder at foxtrialfinder.org.
Whether you have Parkinson’s or not, you can help move research forward. Join the study that’s changing everything. Find out more at michaeljfox.org/podcast-ppmi.
Doctors have been using DaTscan brain imaging as a tool to help diagnose the Parkinson’s disease (PD) for more than a decade, but even people who know a lot about the disease often still have questions about its role — and the role of other imaging tools — in diagnosis and care. What’s a DaTscan, and how does it relate to PET, SPECT and MRI? When is a DaTscan or other brain imaging tool used in PD? Are there any risks?
In this audio from our Third Thursdays Webinar, experts and people with PD offer listeners an impromptu course in Brain Imaging 101. You’ll learn to differentiate the different types of imaging used to visualize the brain and how they are used in PD research and care. You’ll also learn the latest in efforts to visualize alpha-synuclein, the protein that misfolds and clumps in Parkinson’s, and what its selective imaging in the living brain will mean for PD clinical trials and care.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. https://apple.co/3p02Jw0
Whether you have Parkinson’s or not, you can help move research forward. Join the study that’s changing everything. Find out more at michaeljfox.org/podcast-ppmi.
The holidays can be a time of joyful celebration with those we love. They may also come with the stress of travel, disruptions to your regular routine or even loneliness. For those living with Parkinson’s disease (PD), or those taking care of someone they love with the disease, these feelings can be intensified. This podcast offers tips to people living with PD, as well as their care partners, friends and family, for how to prepare — mind, body and suitcase — to make your holidays happy.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. https://apple.co/3p02Jw0
Whether you have Parkinson’s or not, you can help move research forward. Join the study that’s changing everything. Find out more at michaeljfox.org/podcast-ppmi.
In a year of remarkable progress for the Parkinson’s field, we’re entering a new era for better understanding the biology of the disease, with the identification of a breakthrough biomarker accelerating new therapeutics through the clinical pipeline and legislators on Capitol Hill moving toward legislation that unites the federal government on a mission to treat, prevent and cure Parkinson’s disease.
What does this progress mean for researchers studying Parkinson’s and for those living with the disease? And what will come next?
Tune in as scientists and staff from The Michael J. Fox Foundation (MJFF) answer these questions and share insights in our latest Third Thursdays Webinar.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. https://apple.co/3p02Jw0
Join a study today to help speed progress toward better treatments and a cure for Parkinson’s disease. To search for studies in your area, visit Fox Trial Finder at foxtrialfinder.org.
Whether you have Parkinson’s or not, you can help move research forward. Join the study that’s changing everything. Find out more at michaeljfox.org/podcast-ppmi.
In a groundbreaking discovery earlier this year, a global consortium founda new variant in the GBA gene that is associated with a higher risk of Parkinson’s disease (PD) for people of African ancestry. The finding marks the first African ancestry-specific genetic risk factor for Parkinson’s disease. In this podcast, researchers share the human stories behind the discovery, which underscores the importance of international collaboration and the participation of underrepresented communities in research.
Themes covered in this discussion:
- (02:05) – Breaking down the genetic discovery and why it’s important for PD research
- (05:27) – More on the genetic samples that resulted in this discovery
- (06:53) –Why the GBA1 gene is of interest and its connection to PD
- (11:13) – How the Global Parkinson’s Genetics Program (GP2) maintains privacy and confidentiality of data from study participants
- (13:15) – How people should think about genetics as a risk factor for PD
- (14:55) – Capacity building and building community trust
- (19:57) –Why this discovery takes us closer to finding better treatments and a cure for PD
- (21:51) – Story behind accidental discovery of GBA1 variant
- (22:50) – Background on GP2 and excitement on the GBA1 variant discovery
- (33:17) – Ethnicity and health risk factors and other determinants of health
- (35:03) – Importance of diversity, equity and inclusion in science and to The Michael J. Fox Foundation’s mission
- (36:52) – Research in PD historically focused on people of Northern European ancestry
- (38:09) –Why people from underrepresented groups need to lead these studies
- (39:30) – Importance of including underrepresented populations across the research pipeline
- (40:18) –Why research participation is important and how you can get involved
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network.https://apple.co/3p02Jw0
Whether you have Parkinson’s or not, you can help move research forward. Join the study that’s changing everything. Find out more at michaeljfox.org/podcast-ppmi
People with Parkinson’s disease (PD) have lots of questions about probiotics, prebiotics, laxatives and fiber. That’s because constipation and bloating are some of the more bothersome but less talked about symptoms of PD. In this audio from our Third Thursdays Webinar, experts and people with PD discuss effective ways for managing constipation and other gut-related symptoms. You’ll also learn about emerging treatments for constipation, the gut-brain connection and why the gut is linked to Parkinson’s.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. https://apple.co/3p02Jw0
Whether you have Parkinson’s or not, you can help move research forward. Join the study that’s changing everything. Find out more at michaeljfox.org/podcast-ppmi.
Shock, doubt, anxiety — a diagnosis of Parkinson’s can trigger these and many other difficult emotions. This replay of audio from our Third Thursdays Webinar features a conversation among people with Parkinson’s about how they processed the emotional aftermath and navigated the early years following their diagnosis. We also hear from a psychologist who specializes in Parkinson’s about what she’s learned about how people deal with this life-changing diagnosis and ways to manage the emotions in a positive way.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. https://apple.co/3p02Jw0
Whether you have Parkinson’s or not, you can help move research forward. Join the study that’s changing everything. Find out more at michaeljfox.org/podcast-ppmi.
In this replay of audio from our Third Thursdays Webinar, Michael J. Fox Foundation Patient Council member Larry Gifford leads a discussion on common Parkinson’s issues — dyskinesia and "off" time — and how to treat them.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. https://apple.co/3p02Jw0
Whether you have Parkinson’s or not, you can help move research forward. Join the study that’s changing everything. Find out more at michaeljfox.com/podcast-ppmi.
Stem cells have grabbed headlines for decades. Now, at last, they are starting to deliver on their therapeutic promise, with multiple stem cell therapies in clinical trials for Parkinson’s disease. This episode of our award-winning “Parkinson’s Science POV” series brings us up to date on these trials, including how scientists are using stem cells to replace dopamine, the chemical that’s lost in Parkinson's disease.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. https://apple.co/3p02Jw0
Join a study today to help speed progress toward better treatments and a cure for Parkinson’s disease. To search for studies in your area, visit Fox Trial Finder at foxtrialfinder.org.
Whether you have Parkinson’s or not, you can help move research forward. Join the study that’s changing everything. Find out more at michaeljfox.com/podcast-ppmi.
What do you know about gene therapy and its potential for treating Parkinson’s? In this audio from our Third Thursdays Webinar, you’ll learn what exactly gene therapy is and how it works, who gene therapy might work for and the role of genetic testing. You’ll also get a status report on investigations into gene therapy for Parkinson’s. Panelists include experts in the field as well as a person with Parkinson’s and her care partner.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. https://apple.co/3p02Jw0
Whether you have Parkinson’s or not, you can help move research forward. Join the study that’s changing everything. Find out more at michaeljfox.com/podcast-ppmi
How’s this for a dinnertime conversation starter… did you know that what happens in your gut can have an impact on your brain health? Some experts even call the gut “the second brain” because of its huge community of microbes and large nerve network that links the gut to brain disease, like Parkinson’s.
Join our panel of experts who cover the latest research on this link between gut and brain health. And tune in as they discuss common gut symptoms of Parkinson’s and what you can do to manage them.
For more on this topic, visit michaeljfox.org/guthealth.
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Many people with Parkinson’s experience autonomic symptoms, like bladder problems, low blood pressure and constipation that can be hard to talk about. In this audio from our Third Thursdays Webinar replay, experts and patients open a dialogue on these issues and share ways to treat them.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. https://apple.co/3p02Jw0
Whether you have Parkinson’s or not, you can help move research forward. Join the study that’s changing everything. Find out more at michaeljfox.com/podcast-ppmi
In the latest installment of our award-winning “Parkinson’s Science POV” series, MJFF’s Maggie Kuhl sits down with Mark Frasier and Brian Fiske, Chief Science Officers at MJFF, in an “Ask MJFF Anything” edition of our podcast. These experts cover a variety of questions from our community about Parkinson’s disease (PD) therapies and treatments, the recent biomarker breakthrough and more. Get answers on topics ranging from how exercise helps improve balance, to what the new biomarker breakthrough means for the Parkinson’s community.
Whether you have Parkinson’s or not, you can help move research forward. Join the study that’s changing everything. Find out more at michaeljfox.com/podcast-ppmi
Have you ever wondered what’s the best exercise for your brain? Listen as our expert panel breaks down approachable tips to add more movement into your day-to-day, Parkinson’s-friendly exercises to try right now and the science behind the benefits of working up a sweat.
Join hundreds of Parkinson’s community members June 17 weekend for our annual Virtual Run/Walk. Register and learn more at www.michaeljfox.org/runwalk
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Faith and science are not often discussed together, but science requires a leap of faith. A few years ago, MJFF staff scientists, Samantha Hutten, PhD and Katie Kopil, PhD never would have guessed that a leap of faith and a cold call to a researcher in Texas would lead to a tool that, for the first time, can detect Parkinson’s in people who have not yet shown symptoms. With the help of the countless community members taking part in the PPMI study, these researchers found a biomarker for Parkinson’s. Hear all about the journey to the breakthrough and what it means to the Parkinson’s community in this rich discussion with some of the humans behind it.
Whether you have Parkinson’s or not, you can help move research forward. Join the study that’s changing everything. michaeljfox.org/podcast-ppmi
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. https://apple.co/3p02Jw0
In April, The Michael J. Fox Foundation (MJFF) announced a major biomarker breakthrough, opening a new chapter for Parkinson’s research — with the promise of better drug development and care for all people and families living with the disease. With the new test, validated by MJFF’s Parkinson’s Progression Markers Initiative (PPMI), researchers can objectively define and monitor this pathology for the first time in the living body. Experts explain the promise this research holds for all people living with Parkinson’s.
PPMI is enrolling people with and without Parkinson's disease. Join the study that's changing everything. michaeljfox.org/podcast-ppmi
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Did you know that RBD or acting out dreams can be an early indicator of Parkinson’s? Many people develop sleep issues as they age — with and without PD. Join host, Larry Gifford, in a rich discussion with expert Stephen Joza, MD, PhD, and listen to personal accounts from Allen Dance, PPMI participant, and Richie Rothenberg, MJFF Patient Council Member with his care partner Julie Merson, on why sleep is important, strategies to tackle sleep problems and the importance of participating in research studies like PPMI.
The Parkinson’s Progression Markers Initiative, or PPMI, is learning more about the connection between RBD and brain disease to understand who gets Parkinson’s, who doesn’t, and why. And those insights could lead to better treatments and cures.
For more information on RBD, visit michaeljfox.org/dreams.
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From freezing to shuffling and everything in between, gait and balance struggles can impact people with Parkinson’s at all stages of their journey. In this episode, listen as experts discuss emerging research and tips for people and care partners to improve mobility, prevent falls and maintain independence day-to-day.
Our landmark Parkinson’s Progression Markers Initiative is open to anyone over age 18 in the U.S. Join the study that could change everything at michaeljfox.org/podcast-ppmi
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. https://apple.co/3p02Jw0
For many, the word “diet” has negative associations: cutting out the foods you love, not enjoying what you eat or following strict rules about what you can or can’t eat. But diet is a way of life. And you can still boost brain health or manage Parkinson’s with your favorite family recipes, dinner out with friends and even the salty or sweet snacks you crave most. MJFF’s SVP of Medical Communications, Rachel Dolhun, MD, fellowship-trained movement disorder specialist, board-certified neurologist and lifestyle medicine physician, sits down with expert dietitians Paula Montagna and Vanessa Rissetto, and Parkinson’s community members, Denise and Bernard Coley, to answer your most-asked questions on healthy eating and nutrition.
Want to learn more on this topic? Download our new guide on diet and brain health at michaeljfox.org/dietguide.
And for more easy-to-make recipes from today’s episode, visit michaeljfox.org.
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What foods are best for you? Whether you have Parkinson’s disease, or are concerned you might develop it, food and nutrition play a critical role in brain health. Our expert panel shares effective ways to manage symptoms through nutrition and mobility modifications to make food preparation and eating easier.
Learn more about diet and nutrition in our new free guide, available at michaeljfox.org/guides.
Our landmark research study is exploring the connection between smell loss and brain health. If you’re age 60 and up without Parkinson’s, request a free scratch-and-sniff test at mysmelltest.org/partners.
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There are social, emotional and physical changes you may notice after living with Parkinson’s for some time. In this episode replay, experts discuss tips for managing symptoms, finding support and living well with Parkinson’s disease.
Our landmark Parkinson’s Progression Markers Initiative is open to anyone over age 18 in the U.S. Join the study that could change everything at michaeljfox.org/podcast-ppmi
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. https://apple.co/3p02Jw0
Un diagnóstico de Parkinson puede traer muchas emociones diferentes: negación, ira, tristeza, frustración. Es importante saber que no importa qué emociones sientas, no estás solo. Escuche a los expertos, personas con Parkinson y un especialista en trastornos del movimiento, hablar sobre cómo navegar por las emociones y el viaje viviendo con la enfermedad. Este episodio es de nuestro último seminario virtual en español y ofrece reflexiones personales sobre los pasos que las personas y familiares con Parkinson pueden tomar para aceptar y vivir bien con la enfermedad.
Si prefiere escuchar sobre la marcha, suscríbase a nuestro podcast de Parkinson de la Fundación Michael J. Fox en iTunes o a través de cualquier aplicación de podcast en su celular inteligente o tableta. Si le gustó este podcast, compártelo con una amistad o deja una reseña en iTunes. Ayuda a oyentes como usted a encontrar y apoyar nuestra misión.
The Parkinson’s community often asks, “What new treatments are in the pipeline?” In this episode, experts discuss the latest approaches in treating the spectrum of Parkinson’s, from early diagnosis to advancing disease. They also highlight the latest tools to predict and measure Parkinson’s and critical steps toward prevention.
Recently diagnosed with Parkinson’s? You can play a critical role in the Parkinson’s Progression Markers Initiative (PPMI) study. Learn more at michaeljfox.org/podcast-newlydiagnosed
Anyone over age 18 in the U.S. — with or without Parkinson’s, at any stage — can join the online part of PPMI. Get started at michaeljfox.org/podcast-ppmi
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. apple.co/3p02Jw0
Many people and families with Parkinson’s wonder if deep brain stimulation (DBS) — a surgical procedure for Parkinson’s — is a possible treatment option for them. In this episode replay, experts discuss who should consider DBS; potential benefits and risks; and the latest advancements in DBS research.
If you’ve recently been diagnosed with Parkinson’s, you can play a critical role in our landmark Parkinson’s Progression Markers Initiative (PPMI) study. Get started at michaeljfox.org/podcast-newlydiagnosed
Anyone over age 18 in the U.S. — with Parkinson’s, at any stage, or without — can join the online part of PPMI at michaeljfox.org/podcast-ppmi
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. https://apple.co/3p02Jw0
A Parkinson’s diagnosis can bring many different emotions — denial, anger, sadness, frustration. It’s important to know that no matter what emotions you feel, you’re not alone. Listen as people with Parkinson’s and their loved ones discuss how they’ve navigated emotions in the early years with Parkinson’s disease. This podcast episode offers personal reflections on steps people can take toward acceptance and real-world advice for those recently diagnosed and beyond.
If you’ve been diagnosed with Parkinson’s in the past two years, you can play a critical role in the Parkinson’s Progression Markers Initiative (PPMI) study. Learn more at michaeljfox.org/podcast-newlydiagnosed
The online part of PPMI is open to anyone over age 18 in the U.S. Join the study that could change everything at michaeljfox.org/podcast-ppmi
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. apple.co/3p02Jw0
Public policy plays an important role in speeding a cure for Parkinson’s. In this episode, experts discuss ways to become a Parkinson’s advocate and how you can reach out to your elected officials to help influence change on behalf of the Parkinson’s community. Experts also highlight the first-ever legislation solely dedicated to ending Parkinson’s disease.
Ask your Representative to support The National Plan to End Parkinson’s Act at michaeljfox.org/national-plan
Recently diagnosed with Parkinson’s? You can play a critical role in the Parkinson’s Progression Markers Initiative (PPMI) study. Learn more at michaeljfox.org/podcast-newlydiagnosed
The online part of PPMI is open to anyone over age 18 in the U.S. Join the study that could change everything at michaeljfox.org/podcast-ppmi
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. apple.co/3p02Jw0
Many people with Parkinson’s consider telehealth a useful tool for getting care. But for some, the technology or visit may be tough to navigate. In this episode, experts discuss how to make the most of a virtual visit with a doctor and the impact of telehealth on research and care.
Recently diagnosed with Parkinson’s? You can play a critical role in the Parkinson’s Progression Markers Initiative (PPMI) study. Connect with the PPMI team at michaeljfox.org/podcast-ppmi-sites
The online part of PPMI is open to anyone over age 18 in the U.S. Join the study that could change everything at michaeljfox.org/podcast-ppmi
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. apple.co/3p02Jw0
Walking is a complex skill. So, shares Catherine Kopil, PhD, in the third episode of our “Parkinson’s Science POV” podcast series.
Gait requires a symphony of connections between the brain and body, which makes it one of the hardest Parkinson’s symptoms to treat. Kopil, MJFF Senior Vice President of Clinical Research, and Chief Scientific Officer Mark Frasier, PhD, discuss progress toward understanding the neuroscience of gait challenges, such as walking, balancing, shuffling steps and freezing. They talk about treatments in testing and the use of digital technology to measure and predict gait changes in people with PD.
Much of this work is happening in our landmark Parkinson’s Progression Markers Initiative (PPMI) study. Join today at www.michaeljfox.org/podcast-PPMI to contribute to new discoveries and better measures of disease. PPMI especially needs people recently diagnosed with Parkinson’s or with certain risk factors such as smell loss or acting out dreams.
Anyone over the age of 18 in the United States can join through its online platform. Outside the U.S.? View a list of international recruiting sites at www.michaeljfox.org/ppmi-recruiting-sites.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. https://apple.co/3p02Jw0
Parkinson’s can affect the automatic and involuntary functions our bodies perform, like heartbeat and digestion. In this episode, experts discuss common but lesser-known Parkinson’s symptoms — including bladder problems, constipation, low blood pressure and sweating — and what you can do to treat them.
Recently diagnosed with Parkinson’s? You can play a critical role in the Parkinson’s Progression Markers Initiative (PPMI) study. Connect with the PPMI team at michaeljfox.org/podcast-ppmi-sites
The online part of PPMI is open to anyone over age 18 in the U.S. Join the study that could change everything at michaeljfox.org/podcast-ppmi
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. apple.co/3p02Jw0
In honor of Father’s Day, The Michael J. Fox Foundation (MJFF) is sharing a special podcast episode between three adult children who discuss how they each have navigated having a father with Parkinson’s disease.
What is the science behind genetic inheritance that increases the chance of getting Parkinson’s disease (PD) later in life? In this episode, experts explain what genetic mutations are, those that are mostly seen in people with PD and the benefits of genetic testing.
Join the study that could change everything at michaeljfox.org/podcast-ppmi.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. apple.co/3p02Jw0
Did you know the government plays an important role in helping find a cure for Parkinson’s, and in caring for those living with the disease? In this episode, Michael J. Fox Foundation policy experts and grassroots advocates discuss the importance of telling your story and building relationships with elected officials who represent you in the halls of power across the United States.
You can help lawmakers understand what matters to people with Parkinson’s. Join our policy network today at michaeljfox.org/advocacy
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. Apple.co/3p02Jw0
Navigating a Parkinson’s diagnosis can be challenging, but you’re not alone. In this episode replay, experts share practical tips for managing the early years of Parkinson’s disease.
If you’ve recently been diagnosed with Parkinson’s, you can play a critical role in our landmark Parkinson’s Progression Markers Initiative (PPMI) study. Connect with the study team today at michaeljfox.org/podcast-ppmi-sites.
Anyone over age 18 in the U.S. — with Parkinson’s, at any stage, or without — can join the online part of PPMI. Get started at michaeljfox.org/podcast-ppmi.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. https://apple.co/3p02Jw0
How is Parkinson’s diagnosed? Tracked? Importantly, predicted? In the second episode of our “Parkinson’s Science POV” podcast series, MJFF Chief Scientific Officers discuss progress toward better tests for Parkinson’s disease, including a recent report of a brain scan of a key Parkinson’s protein. They discuss imaging, fluid measures and wearable devices and how these objective tools could speed new treatments and improve care.
Much of this work and findings stem from our landmark Parkinson’s Progression Markers Initiative (PPMI) study. Join today at https://michaeljfox.org/podcast-PPMI to contribute to new discoveries and better measures of disease. PPMI especially needs people recently diagnosed with Parkinson’s or with certain risk factors such as a relative with the disease, smell loss or acting out dreams. Anyone over the age of 18 in the United States can join through its online platform. Outside the U.S.? View a list of international recruiting sites at https://www.michaeljfox.org/ppmi-recruiting-sites.
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. https://apple.co/3p02Jw0
We all dream when we sleep. Some don’t remember dreams. Others clearly recall what they did, how they felt, and who else was there. Still others unintentionally act out their dreams. They may imagine catching a touchdown pass, running from a wild animal, or fending off an enemy. In this episode, our on-staff movement disorder specialist speaks with a couple about their experience with acting out dreams, called REM sleep behavior disorder.
If you or your bed partner act out your dreams — whether you have Parkinson’s or not — you can play a critical role in research. Join the study that could change everything at michaeljfox.org/podcast-ppmi
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. apple.co/3p02Jw0
Some people act out their dreams while asleep. They may punch, kick, yell or even fall out of bed. This sleep problem can be linked to Parkinson’s and other brain diseases. In this episode, experts share why sleep issues happen and what you can do to manage them.
If you or your bed partner have sleep issues — whether you have Parkinson’s or not — you can play a critical role in research. Join the study that could change everything at michaeljfox.org/podcast-ppmi
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. apple.co/3p02Jw0
Sexual problems are common in people with Parkinson's, but they can be difficult to talk about. In this episode, experts discuss how Parkinson’s and associated symptoms like sleep changes impact relationships and they share strategies for improving physical and emotional intimacy.
A deeper understanding of Parkinson’s disease biology could improve every available treatment. You can help us achieve that. Our landmark Parkinson’s Progression Markers Initiative is open to anyone over age 18 in the U.S. Join the study that could change everything at michaeljfox.org/podcast-ppmi
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. apple.co/3p02Jw0
People with Parkinson's often ask how diet and exercise fit into their overall care plan. In this episode, experts share what you can do today to eat healthier, exercise, boost brain health and live well as you age.
Our landmark Parkinson’s Progression Markers Initiative is open to anyone over age 18 in the U.S. Join the study that could change everything at michaeljfox.org/podcast-ppmi
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. apple.co/3p02Jw0
Parkinson’s disease changes: its biology and symptoms start even before the cardinal movement issues and evolve decades after diagnosis. In the first episode of our new podcast series “Parkinson’s Science POV,” MJFF Chief Scientific Officers discuss strategies to stop disease progression at every stage. This episode covers our Foundation’s approach to preventing cognitive changes and falls and to moving toward a world where no one receives a diagnosis of Parkinson’s disease.
You can play a part in research, too. Our landmark Parkinson’s Progression Markers Initiative is open to anyone over age 18 in the U.S. Join the study that could change everything at michaeljfox.org/podcast-ppmi
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. https://apple.co/3p02Jw0
Over the past decade, The Michael J. Fox Foundation’s landmark Parkinson’s Progression Markers Initiative has changed how research is done and what scientists know about the brain. Listen as experts discuss the study’s expansion and why now it needs you.
PPMI is open to anyone over age 18 in the U.S. Join the study that could change everything at michaeljfox.org/podcast-ppmi
People early in their disease course are valuable partners in research working toward cures. Experts discuss why this is so important for The Michael J. Fox Foundation’s landmark Parkinson’s Progression Markers Initiative (PPMI) and the critical role you can play in research.
Recently diagnosed with Parkinson’s? Connect with the PPMI team today at michaeljfox.org/podcast-ppmi-sites
PPMI is open to anyone over age 18 in the U.S. Join the study that could change everything at michaeljfox.org/podcast-ppmi
Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. https://apple.co/3p02Jw0
Hear expert panelists discuss the latest advancements in Parkinson’s research for our 2021 research review webinar.
In this podcast, we recap the discussion from our Research Roundtable's expert panel of scientists, program leaders and a person with Parkinson’s.
Hear our panelists discuss common Parkinson’s issues — "off" time and dyskinesia — and how to treat them.
What is an “off” period in Parkinson’s? Why does it look so different from person to person? And how do you manage these episodes? Experts discuss steps to work with your doctor and care partners to manage these times when medication is wearing off between doses.
Tune in to part two of this podcast takeover as the global advocacy group — the PD Avengers — highlights more Parkinson’s organizations from all over the world. Connect with new groups, learn about their mission and find resources that can support you and your family in your journey with the disease.
Ever wondered why there are so many Parkinson’s organizations around the world? Join the PD Avengers — a global advocacy group — as they take over MJFF’s podcast to understand what sets each organization apart, and how you can get involved today.
Hear expert panelists discuss who should consider deep brain stimulation, a surgical procedure for Parkinson’s.
Learn about how you can join the Foundation’s new online community — the Parkinson’s Buddy Network — to build meaningful connections with other people and families navigating the disease.
Hear expert panelists offer ways to manage isolation and loneliness and tips for creating meaningful community connections.
Hear our expert panelists discuss the benefits and risks of participating in Parkinson’s research.
Hear from our on-staff movement disorder specialist about the latest in Parkinson’s care and research.
Hear our expert panelists discuss thinking and memory changes that can happen in Parkinson’s.
Hear our expert panelists offer practical tips for navigating a new Parkinson’s diagnosis.
Our experts share information, strategies and tips for living with or caring for someone with mild thinking and memory changes.
Hear our expert panelists offer practical tips and strategies for managing sleep issues in Parkinson’s disease.
Hear from our on-staff movement disorder specialist about the latest in Parkinson’s care and research.
Listen to part two of our conversation reviewing research highlights from the 20-year history of The Michael J. Fox Foundation. And learn about the next chapter the Foundation is just beginning to write.
Tune in and walk down memory lane as Foundation leaders reflects on 20 years of milestones and momentum in Parkinson’s research.
Our panelists share the momentum happening in Parkinson’s research and what’s on the horizon in 2021.
Hear from our on-staff movement disorder specialist about the latest in Parkinson’s care and research.
Listen to the second part of our fall preview as Foundation staff recap recent events and look forward to what activities and offerings are right around the corner.
This election season, we review what’s on the ballot and how these decisions impact the Parkinson’s community.
Listen to our panelists discuss what we know about Parkinson’s genetics and how genetic discoveries may lead to new treatments to stop or prevent disease.
Michael J. Fox Foundation staff discuss devices in testing to treat gait freezing and swallowing problems.
Hear from our on-staff movement disorder specialist and her guest, MJFF Board Member Jeff Keefer, diagnosed with Parkinson’s in 2007, about PD care and research.
In this episode of The Michael J. Fox Foundation Parkinson's Podcast, we roll out the “orange carpet” so to speak and give you a first look at the virtual activities, events and new resources the Foundation is putting together for the fall.
A virtual run/walk. A fireside chat with Michael J. Fox. And much, much more. Listen as our panelists give you an insider update on what’s coming down the pike and how you and your family can take part. Everyone here at the Foundation looks forward to connecting with the community this fall. Visit michaeljfox.org/here to learn more.
Rather listen on-the-go? Subscribe to our Michael J. Fox Foundation Parkinson's Podcast on iTunes or through any podcast app on your smartphone or tablet. And if you enjoyed what you heard, share it with a friend or leave a review on iTunes. It helps listeners like you find and support our mission.
Expert Panelists:
Host and person with Parkinson's Larry Gifford leads a discussion with:
Rachel Dolhun, MD, vice president of medical communications at MJFF and a board-certified movement disorder specialist
Holly Teichholtz, chief marketing officer at MJFF
Hear from our on-staff movement disorder specialist about the latest in Parkinson’s care and research.
Listen to our panelists discuss how environmental factors may lead to Parkinson’s and policies to limit those exposures.
In this episode of The Michael J. Fox Foundation Parkinson's Podcast, we explore the intersection of race and Parkinson’s in both the lived experience of obtaining care for the disease and how that translates to research.
Listen as our panelists have a candid conversation about the value of inclusivity to advance the field’s understanding of the disease and ultimately, more scientific breakthroughs. And learn about how the Foundation is working today to break down barriers to recruit and retain underrepresented communities to participate in research.
Rather listen on-the-go? Subscribe to our Michael J. Fox Foundation Parkinson's Podcast on iTunes or through any podcast app on your smartphone or tablet. And if you enjoyed what you heard, share it with a friend or leave a review on iTunes. It helps listeners like you find and support our mission.
EXPERT PANELISTS
Host and person with Parkinson’s Larry Gifford leads a discussion with:
Jonathan Jackson, PhD, founding director of Community Access, Recruitment, and Engagement (CARE) Research Center at Massachusetts General Hospital and principal investigator of the Fostering Inclusivity in Research Engagement for Underrepresented Populations in Parkinson’s Disease (FIRE-UP PD)
Bernadette Siddiqi, Associate Director of Research Partnerships at MJFF
María L. De León, MD, movement disorder specialist, MJFF Patient Council member and policy advocate
View a transcript of this podcast.
EXTRA READING:
Share Your Story -- The Michael J. Fox Foundation is seeking to grow its community by sharing diverse experiences and perspectives from all who are touched by Parkinson’s disease. If interested, please email your story to shareyourstory@michaeljfox.org along with the best contact information to reach you. We may share your story in future communications.
Get Involved in Research -- Learn more about Parkinson’s clinical research, who can participate and what types of studies are available. Download MJFF’s free guide to Navigating Clinical Trials, which is available in several languages, including Spanish.
In this episode of The Michael J. Fox Foundation Parkinson's Podcast, we discuss the importance of voicing your Parkinson’s priorities on Capitol Hill and how that might look different during a pandemic. Stepping into his new role as host of the podcast, Foundation Patient Council member Larry Gifford leads a conversation with Ted Thompson, JD, Senior Vice President of Public Policy at MJFF, and Israel Robledo, MJFF Patient Council member and policy advocate, about:
Why what happens in Washington, D.C. matters to people with Parkinson’s
Why grassroots advocacy is important and how members of Congress need to hear from constituents
How you can get involved today to advocate for COVID-19 related telemedicine and mental health policy asks that could impact our community
Interested in Parkinson’s advocacy? We need your help to take action. Sign up here.
Listen to our panelists discuss results from our Fox Insight survey on the coronavirus and Parkinson's disease.
Hear from our on-staff movement disorder specialist about the latest in Parkinson’s care and research.
Listen to our panelists discuss how depression and anxiety in Parkinson’s impacts life and care.
Larry Gifford and guests explore ways to stay connected and ease anxiety while living with Parkinson’s in a time of uncertainty.
Larry Gifford and guests break down the importance of keeping a healthy mind and body after a Parkinson’s diagnosis and especially during COVID-19.
Larry Gifford and expert guests discuss how COVID-19 is affecting Parkinson’s research.
In our first episode, we dive into practical tips for managing your Parkinson’s during COVID-19. Michael J. Fox Foundation Patient Council member Larry Gifford leads a conversation with Rachel Dolhun, MD, a board-certified movement disorder specialist and Vice President of Medical Communications at MJFF, and, Katie Amodeo, a movement disorder specialist at the University of Rochester and a graduate of the Edmond J. Safra Fellowship in Movement Disorders, about:
Getting the most out of telemedicine
The impact of social distancing on those who need in-home care
DBS care
Managing stress and anxiety
Rather listen on-the-go? Subscribe to our Michael J. Fox Foundation Parkinson's Podcast on iTunes or through any podcast app on your smartphone or tablet.
Listen to our panelists discuss how the coronavirus could impact people with Parkinson’s and actions you can take to manage new changes and challenges.
Listen to our expert panelists discuss sexual changes women and men with Parkinson’s can experience.
Hear from our on-staff movement disorder specialist about the latest in Parkinson’s care and research.
Listen to our expert panelists discuss guidelines and considerations for a healthy diet with Parkinson’s.
Listen to our on-staff movement disorder specialist and research leads answer your questions.
Hear from our on-staff movement disorder specialist about the latest in Parkinson’s care and research.
Foundation staff discuss how inflammation can be both bad and good and how studying its connection to Parkinson’s could help define, measure and treat disease.
Listen to our expert panelists talk about medical marijuana, and other complementary therapies, for Parkinson’s disease.
Hear from our on-staff movement disorder specialist about the latest in Parkinson’s care and research.
Listen to our expert panelists talk about cognitive changes in Parkinson’s, strategies to reduce them and research toward new therapies.
Listen to our expert panelists talk about stem cells as a research tool and potential therapy for Parkinson’s.
Hear from our on-staff movement disorder specialist about the latest in Parkinson’s care and research.
Hear from our on-staff movement disorder specialist about the latest in Parkinson’s care and research.
Panelists discuss how inflammation may play a role in Parkinson’s and treatments using immune system properties against disease.
Scientists discuss how reading the sequence of genes and proteins can help better define, measure and treat Parkinson's disease.
MJFF and NINDS leaders discuss results from trials of a dietary supplement and a blood pressure drug for Parkinson's and what is next in the pipeline.
The Michael J. Fox Foundation's Dr. Marco Baptista, Sohini Chowdhury and Dr. Rachel Dolhun talk to Dave Iverson about recent findings and new programs.
Staff from The Michael J. Fox Foundation answer questions from the audience at a recent panel discussion on progress in Parkinson's research.
In this Third Thursdays Webinar, physicians and people with Parkinson's discuss strategies to make doctor visits more effective and efficient.
Listen to our expert panelists talk about medical devices that can manage certain Parkinson's symptoms.
Our panelists in this Third Thursdays Webinar discuss common Parkinson's motor symptoms and emerging treatments to target them.
https://www.michaeljfox.org/foundation/news-detail.php?new-parkinson-drug-comes-to-market-after-early-investment-from-the-michael-fox-foundation
Hear our panelists and co-authors of the paper "The Parkinson's Pandemic" discuss reasons for this global rise and strategies to contend with the issue.
Listen to our expert panelists discuss the progress made in PD research over the last year and what to look forward to in 2019.
Listen to Dr. Rachel Dolhun's tips for making the most of holiday visits with family who have Parkinson's.
In our latest podcast, listen to our Third Thursday Webinar panelists discuss 'off' times in Parkinson's.
Hear from our on-staff movement disorder specialist about dystonia: a symptom of Parkinson's and standalone disorder that causes painful muscle cramps.
One of our MJFF scientists talks about piecing together the many factors that play a role in Parkinson's and what can help us continue making progress.
MJFF scientist Dr. Brian Fiske talks about what goes wrong with cellular proteins, how we may fix them and if you should eat less protein.
Dr. Ray Dorsey from the University of Rochester discusses the rise in Parkinson's and how we can take steps to prevent onset and get people the care they need.
Missed our Year in Review webinar? Catch up with this recording and hear our panelists recap new potential Parkinson's treatments in clinical testing.
Autophagy is how cells break down and recycle damaged parts. We explain the link to Parkinson's and how treating autophagy may slow or stop disease.
The online study Fox Insight analyzes data on life with disease from tens of thousands of people, with or without PD, to influence research focus and design.
How does dyskinesia impact people with PD? An MJFF-funded measurement scale captured those perceptions and helped a new drug get approved to treat it.
Scientists are testing drugs used for high blood pressure and diabetes for their effects on Parkinson's disease. MJFF CEO Todd Sherer, PhD, discusses this tactic of drug repurposing.
In the latest in our "Getting to a Cure: Science behind the Search" series, we cover the proposed connection between sticky protein alpha-synuclein and the immune system.
Nancy Mulhearn, who was diagnosed with Parkinson’s at age 44, shares her experiences with the disease.
Carlos Singer, MD, of the University of Miami discusses common sleep problems in Parkinson's and how to treat them.
Urinary function is governed by the body's autonomic nervous system. In Parkinson's, urinary function can be thrown off balance, but urinary problems aren't always recognized by patients.
Learn more at https://www.michaeljfox.org/clinical
Barbara and Jay Robinson discuss their decision to participate in Parkinson's genetics research.
Sarkis Mazmanian, PhD, of CalTech discusses what we know about the gut bacteria and Parkinson's connection in our "Getting to a Cure: The Science behind the Search" podcast series.
Dr. Jamie Eberling, PhD, dicusses alpha-synuclein, a protein that clumps in brain cells of nearly everyone with Parkinson's disease.
In this podcast, Thomas Davis, MD, of Vanderbilt University Medical Center, speaks about how doctors and patients work together to create a medication regimen.
In this podcast, MJFF staff scientist Marco Baptista, PhD, discusses the genetics and biology of LRRK2 and the role of the Foundation in advancing development of LRRK2 therapeutics.
Alex Pantelyat, MD, assistant professor of neurology at Johns Hopkins University, speaks to MJFF about atypical parkinsonisms and their relation to Parkinson’s disease.
In this podcast, Dr. Julie Pilitsis speaks about Parkinson's pain and its connection to fatigue.
Dr. Rachel Dolhun explores Parkinson's disease psychosis, including hallucinations and delusions, and discusses treatments for this symptom.
MJFF's Dr. Brian Fiske discusses how we may be able to target treatments to the "type" of Parkinson's one has, much like is done in cancer care.
MJFF's Samantha Hutten, PhD, talks about how researchers are developing methods to identify people with PD earlier in the disease process, which could help test therapies to slow or stop Parkinson's.
In our latest podcast, Dr. Ole Isacson, MD, PhD, a professor of neurology and neuroscience at Harvard Medical School, discusses stem cells and Parkinson's disease.
In our latest podcast, Christopher Bishop, PhD, discusses what may cause involuntary movements called dyskinesia with long-term Parkinson's disease and medication use.
In our latest podcast the creator of Liftware talks about how he developed his tremor-stabilizing technology and how it helps people with Parkinson's fight isolation.
Mark Frasier, PhD, Senior Vice President of Research Programs at MJFF, discusses Parkinson's disease research highlights from 2015.
Dr. Chris Hass of the University of Florida explores balance, posture and gait issues and how to best protect from falls.
In our latest podcast, MJFF Contributing Editor Dave Iverson speaks with guest panelists about what dance offers people living with Parkinson's.
MJFF CEO Todd Sherer, PhD, discusses therapies in human testing that have potential to slow or stop Parkinson's disease.
In our latest podcast Allison London shares how her dystonia has impacted her life and why she's on a mission to raise awareness.
Jon Palfreman has a new book exploring the history of Parkinson's research. He was diagnosed with PD in 2011 after spending years investigating rare cases of the disease for a documentary and book.
MJFF's Dr. Jamie Eberling talks to Dave Iverson about what cognitive symptoms people with PD may experience and what new therapies are in development.
Dr. Laurie Mischley discusses some of the challenges that research into complementary and alternative approaches to managing Parkinson's face.
MJFF Contributing Editor Dave Iverson recently sat down with Sam to talk about how he turned his athletic talents into a career that honors his mother and the millions of others affected by PD.
Our latest podcast covers how researchers are investigating ways to expand the current capabilities of deep brain stimulation.
Geneticist Dr. Tatiana Foroud explains how the study of Parkinson's genetics can help develop new therapies.
Dr. Lisa Shulman from the University of Maryland discusses how exercise may help manage Parkinson's motor and non-motor symptoms in our latest podcast.
In our latest podcast. MJFF CEO Dr. Todd Sherer discusses the progress in Parkinson's research seen this year.
We say Parkinson’s disease is different for each person, but there are a couple things all people with PD share: Lewy bodies and dopamine loss.
Dystonia is the third most common movement disorder and a symptom of Parkinson's disease. Bonnie Strauss talks about her experience, and Dr. Rachel Dolhun shares what we know about dystonia.
Dr. William Marks talks to Dave Iverson about how wearable devices may help people with Parkinson's monitor their disease and help researchers test new therapies.
Scientists have found six new gene variants associated with Parkinson's, which could point to new treatment paths.
CEO Todd Sherer, PhD, talks to Dave Iverson about why levodopa loses efficacy over time and new therapies in development to even out on/off cycles.
Mark Frasier, PhD, VP of research programs at MJFF, discusses what we know about the overlap between Alzheimer's and Parkinson's diseases.
The experience of Parkinson's disease is different for each patient. Studying that variability may allow researchers to develop personalized treatments for different subtypes of PD.
Tanya Simuni, MD, principal investigator of the STEADY-PD, and MJFF CEO Todd Sherer talk about the study of isradipine, recently granted $23 million from the NIH for Phase III testing.
Biological commonalities between Parkinson's disease and other movement disorders could help researchers develop therapies that could apply across diagnostic barriers.
Charles Adler, MD, PhD, talks to Dave Iverson about autonomic dysfunction symptoms and their place in research in our latest podcast.
Dr. Kathleen Shannon of Rush University talks to Dave Iverson about the need for a definitive Parkinson's diagnostic test, what researchers are doing to develop one and how patients can help.
The SURE-PD study published in JAMA Neurology reports that with medical supervision, it is possible to safely raise levels of the antioxidant urate by taking the urate precursor inosine.
The Michael J. Fox Foundation Contributing Editor Dave Iverson speaks with Kalpana Merchant, PhD of Eli Lilly and Company about the latest in Parkinson's disease research.
Researchers are improving on the existing DBS technology—an implanted electrode delivers electrical pulses to stimulate or block brain signals—and how we use it.
Levels of alpha-synuclein in the brain—measured through imaging tools—could be a biomarker that would help researchers diagnose the disease better and test potential therapies faster.
Contributing Editor Dave Iverson reports on the new technology that partnership will employ and the current state of stem cell research in Parkinson’s disease. He speaks
While much research into Parkinson’s disease (PD) focuses on improving dopamine supply, there is an emerging scientific understanding that Parkinson’s goes well beyond the dopamine system.
The evolution of our understanding of genetics’ role in Parkinson’s disease (PD) and how that understanding will translate into drug discovery is the topic of a new podcast and upcoming Webinar.
Fox Trial Finder volunteer Gwen Schroeder recounts her first clinical trial experience to MJFF contributing editor Dave Iverson.
Dave Iverson speaks with the CEO of Civitas, Glenn Batchelder, and MJFF staffer Maurizio Facheris, MD, MSc to learn more about how the drug works, as well as next steps.
Dave Iverson speaks with Foundation staffer Mark Frasier to learn more about some of the early findings from the study.
Dave Iverson reports on recent disappointing clinical trial results of Ceregene’s trophic factor therapy CERE-120.
Studies have long suggested that smokers may be less likely to get Parkinson's. Here, Dave Iverson speaks with a researcher investigating the potential of nicotine patches as a PD treatment.
2013 could be a pivotal year in PD research, with expected developments on a variety of fronts. In this podcast, Dave Iverson speaks with Foundation staffers about some of that lies ahead.
Emerging evidence over the past 15 years has led researchers to believe that genetics plays a far greater role in Parkinson’s disease (PD) than was once thought.
Patients have always been at the heart of what we do at The Michael J. Fox Foundation. Our dedication to improving patients’ quality of life has shaped our research priorities.
While levodopa is the gold standard therapy for Parkinson's disease (PD), current delivery methods have their limitations.
Understanding the genetics of Parkinson’s disease could be a game changer in developing new treatments for the disease. Especially when it comes to two genetic targets: LRRK2 and alpha-synuclein.
Dyskinesia refers to the excessive and uncontrollable movements that are a side effect of long-term dopamine replacement therapy in patients with Parkinson's disease (PD).
This fall, The FDA recommended that Teva Neuroscience’s drug rasagiline, brand name Azilect, should not be granted status “to slow the clinical progression of PD.”
This past October, Austrian biotech AFFiRiS announced $1.5 million in funding from MJFF for an early stage clinical trial of a first-of-its-kind vaccine approach to treating Parkinson's disease (PD).