This podcast is for people with Parkinson's, Parkinson's care partners and Parkinson's providers. You'll hear from movement disorder specialists, neurologists, psychiatrists, physical and occupational therapists, complementary therapists, people with Parkinson's and Parkinson's care partners on how to live well with Parkinson's today. more

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. more

How can people with Parkinson's live a better life today? Join the Parkinson's Foundation as we highlight the treatments and techniques that can help all people affected by Parkinson's live a better life today, as well as the research that can bring a better tomorrow. View more information on our episodes by visiting parkinson.org/Podcast. Share your comments and thoughts at parkinson.org/Feedback. more

The Secret Life of Parkinson's is a podcast created by Parkinson's patients, sharing their stories and interviewing others, on things we deal with on a daily basis. It's hard for people with PD to talk to others about the disease because sometimes it's difficult for the patient themselves to describe what they are feeling. Talking to other PD patients helps us express what we are going through in ways we might not be able to express to family and friends. more

Have you ever wished there was a source of information about Parkinson's Disease, and resources for persons with PD, that were concise and easy to digest? Look no further than the Parkinson's Disease Education Podcast.In this podcast we attempt to demystify the disease and to empower you to reach your true potential as a person with PD. more

The Parkinson's Experience is a podcast hosted by a Person with Parkinson's (PWP) and based on her daily experiences. Listen in on her journey living with the disease and how she lives her best life with humor, generosity, empathy and knowledge. Her conversations with experts and patients like you are fascinating and authentic. They cover relevant topics from DBS (Deep Brain Stimulation) to exercise to diet to medications to much more difficult subjects like personal relationships. Of the few podcasts available on this topic, don't skip this one from the viewpoint of a patient. Thank you to my sponsor Boston Scientific, the maker of Vercise Genus, a Deep Brain Stimulation or DBS system. To learn more about Parkinson's treatment options, please visit DBSandMe.com more

Hosted by online magazine Parkinson's Life and supported by Parkinson's Europe, this free podcast explores the reality of life with Parkinson's and shares ideas on how to live well with the world's fastest growing neurological condition. Join us for honest conversation, useful information and inspiring stories from around the world. #ParkinsonsLife #Parkinsons. parkinsonslife.eu Hosted on Acast. See acast.com/privacy for more information. more

On Time is a podcast about living with Parkinson's disease (PD). People in the Parkinson's community share their candid stories of daily living with the disease.  The podcast is a program of the Brian Grant Foundation. Learn more about the Brian Grant Foundation at briangrant.org. more

Subscribe for a wonderful cross section of discussions ranging from people with Parkinson's Disease to those who work in the medical, fitness, and research space. Power Over Parkinson's (POP) is a foundation supporting the use of exercise and wellness to reduce the symptoms or slow the progression of Parkinson's Disease. To learn more visit us at poweroverpd.org more

Diagnosed with Young Onset Parkinson's in 2019, Daniel shares honest stories about the emotional, physical, and spiritual impact of living with the disease. Parkinson's and Me offers encouragement, practical insight, and a mindset of hope and resilience. Whether you're newly diagnosed or adjusting to life with Parkinson's, this podcast reminds you that you're not alone and that it's possible to move forward with purpose, faith, and strength. more

'The Caring Neurologist' - By Dr. Sandeep Thakkar is a podcast exploring the science, stories, and breakthroughs shaping the lives of those with Parkinson's and movement disorders. Join Dr. Thakkar as he blends cutting-edge science with compassionate storytelling to empower patients, caregivers, and providers. more

Teresa Jackson from Lean On Me Coaching, shares resources and strategies for thriving with Parkinson's. Join her and her guests to learn how to live your best life in spite of living with a chronic illness.Opinion Disclaimer:The views and opinions expressed in Parkinson's Pathway Pals Tuesdays with Teresa, are those of the guests and do not necessarily reflect the official policy or position of Teresa Jackson and Parkinson's Pathway Pals Tuesdays with Teresa. Any content provided by our guests are of their opinion and are not intended to malign any religion, ethnic group, club, organization, company, individual or anyone or anything and is not intended as medical advice. more

A close look at an extraordinary life with Parkinson's Disease. Quirky and irreverent hosts Judy & Travis take a look at this most tragic of events: life with an incurable disease and why it's important to declare that I'm Not Dead Yet! Start making the changes to get you the best quality of life possible. Updates (usually) every other Monday. more

In this podcast, The Michael J. Fox Foundation for Parkinson's Research brings you right to the cutting edge of neuroscience to discuss the latest discoveries in the field of neuroscience, with a focus on Parkinson's disease (PD). We are working at the forefront of PD research to accelerate scientific breakthroughs by providing funding opportunities, tools and resources to develop new treatments, find cures and improve quality of life for people living with Parkinson's disease.If you're a scientist, clinician or industry professional interested in gaining in-depth insights into the latest advances in basic science, translational research and clinical trials for new therapies and therapeutics, this show is for you. Our host Dr. Marie McNeely interviews experts on topics such as the impacts of genetics, mechanisms of neurodegeneration, neuroimaging, biomarkers, diagnostics, applications of machine learning and artificial intelligence, drug development, novel treatment technologies and more. Subscribe to stay up to date on key developments in neuroscience, neurology, neurodegeneration and Parkinson's disease research. more

Stay up to date on novel, clinically-relevant research findings in Parkinson's disease and other movement disorders. Each episode of the International Parkinson and Movement Disorder Society podcast discusses a relevant development in the field, including highlighted journal articles and interviews with the authors. more

Live Parkinson's - Live an Exceptional Life Discover hope, resilience, and practical tools for living an exceptional life with Parkinson's. Hosted by Chris Kustanbauter, this podcast is dedicated to empowering those with Parkinson's to take charge of their lives and thrive through a holistic approach. Each week, tune in for expert interviews, personal stories, and actionable tips covering exercise, nutrition, optimism, and social connection all proven to improve quality of life. From managing symptoms to staying active and building meaningful relationships, this podcast will equip you with tools and insights to navigate life confidently and positively. Whether you're newly diagnosed, a seasoned warrior, or a caregiver, Live Parkinson's, Live an Exceptional Life brings you evidence-based strategies and inspiring stories to help you overcome challenges and stay motivated on your journey. Let's embrace each day with strength, laughter, and community and live life on your terms. Subscribe now to join our supportive community, and never miss an episode as we tackle Parkinson's together one exceptional day at a time! Subscribe on YouTube - Live Parkinson's Live an Exceptional Life - From Tremors to Triumph Visit: https://www.liveparkinsons.com/ #Parkinsons #LiveExceptional #QualityofLife #Inspiration #Community #LiveParkinsons, #Tremorstotriumph #ParkinsonsWarriors #SpectacularLife Get my book - Spectacular Life - 4 Strategies for Living with Parkinson's - My Journey to Happiness - available on Amazon in paperback or Kindle (e-book) more

I'm Andi Brown, the creator and host of Parky Conversations. I was diagnosed at the age of seventy.  I discovered that writing my blog, Moving and Shaking, afforded me a vehicle for coping with, and even laughing at, my disease, and at aging in general.  In Parky Conversations, I will talk about my own experiences with PD, I'll introduce us to some of my fellow 'Parkies,' and I'll  interview physicians and scientists who are studying aspects of the disease such as the surge in creativity in some, the ability to detect Parkinson's by the way someone smells, and why people see insects cavorting in their underwear.  There are around one million Americans living with Parkinson's right now.  Listen up and learn about an illness that no one ever expects, that presents daily challenges and that sometimes we just have to laugh at.  more

Podcast sharing our journey with dad's Parkinson's,with some humor and recipes too. 

Park Right Here is an informational and hopefully entertaining podcast about Parkinson's disease with husband and wife walking this road together. Jim and I both want this podcast to be more than just about PD. Our desire is to give hope, to inspire and educate PWPs (people with Parkinson's), friends, family, medical professionals, physical therapists, nurses, PCMs, pharmacists, support groups, personal trainers, home health aides, pastors/spiritual advisors, occupational therapists, neighbors, and anyone who wants to support those with PD. We want to let you know that you are not alone. We want to share our personal stories with you. They can at times be funny, sad, hopefully inspiring, difficult, and life-changing. This podcast will have episodes on various topics. An important one is your diagnosis. We will share experiences, trials, and lessons that we both have learned through our journeys. We will discuss the importance of being your own best advocate or one for those you love, basic information about medication, what is and how to choose your care team, what a movement disorder specialist is, how important exercise is for PD, the latest trials and clinical research, tips and tricks on getting through the day, nutrition, the good and bad about supplements and natural remedies, the importance of a support group, what to do when you don't have a support group nearby, how to find support on social media, the importance in talking about PD with others. We both want to make it clear that WE ARE NOT medical professionals or experts in medications, treatments, or even PD. We are lay people just like you and we will be sharing OUR experiences regarding OUR journeys with PD. We want you to take what helps you and discard the rest. We also want to EMPHASIZE that if you have any questions about any medication, speak to your doctor, neurologist, movement disorder specialist, or pharmacist. We want to be transparent and honest. We will not sugarcoat how difficult dealing with PD can be or hide our bad days. What you hear and see, is what you get. We want you to know that PD affects every aspect of your life and those around you, but it shouldn't stop you from living the best life you can. We will interview people who work with and are associated with PD. For example, a movement disorder specialist, physical and occupational therapists, the CEO of LSVT, PWR (Parkinson's Wellness Recovery) PD exercise group, medical professionals, those involved in clinical research, those that work for nonprofit organizations like Michael J Fox foundation and Davis Phinney Foundation, psychologists, family and caregivers, those with PD, and the many inventors and entrepreneurs who are working on treatments and items to help improve our quality of life. Possibly even Micheal J Fox himself. An important part of this podcast is that every listener can be involved. It is our podcast. We want the ideas and questions that you have about PD. We want to hear what topics you would like to discuss. It's important to understand if you violate guidelines, use bad language, bully/troll, or are disruptive, you will be reported and blocked. If you threaten or we believe you are a danger to yourself or others, We will report any comments and posts that we deem necessary for you to get the help that you need. We are so excited to share this with you and we hope it helps you understand what PD is and how to walk through this journey with hope and joy. Thanks for listening and supporting our dream. more

Join us as we chat with members of the YOPD community Disease, care partners and experts in the YOPD field to learn more about this neurodegenerative disease and those living with it. more

You, Me, and PD is a unique conversation between Jeremy Likness who was diagnosed with young-onset Parkinson's Disease in early 2020, and his caregiver and wife, Doreen. They host candid conversations about living with Parkinson's Disease, share stories and tips, and discuss the physical and emotional impact of the diagnosis. Learn about their approach to exercise, nutrition, supplements, faith, estate planning, and coping with grief. Join them on a special journey through challenge and triumph and share in their combined hope for a cure on the horizon. more

Short podcasts, generally under 10 minutes, looking at all things Parkinson's. https://parkinsonsassociation.org more