128 World Parkinson Congress Comes to Phoenix in 2026
The Parkinson's Experience podcast
The World Parkinson Coalition is bringing its triennial World Parkinson Congress to Phoenix in May 2026—the first time the Congress has been hosted in the U.S. since 2016. This is truly a can’t-miss event for anyone in the Parkinson’s community. The Congress will bring together approximately 4,000 attendees from around the world, including researchers, healthcare professionals, people with Parkinson’s, and care partners. It’s a unique opportunity to learn about the latest research, emerging therapies, and the global effort to improve care—while also connecting with an incredible...
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127 Warriors Not Worriers -The InMotion Wellness Program
The Parkinson's Experience podcast
This year I have been highlighting some of local areas in the U.S. where people with Parkinson’s take classes designed for their needs, provide social support, and community. It is truly magical to have this kind of central location just focused on your needs as a person with Parkinson’s. Just last month we highlighted Parkinson’s Body & Mind in Connecticut. They have done and continue to provide spaces where PWP can gather for exercise, wellness and community programs – all for free. If you didn’t listen to that episode, check it out soon. In this episode, we talk with the...
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126 Dystonia Explained
The Parkinson's Experience podcast
While often overshadowed by better known movement disorders, dystonia affects thousands and can dramatically affect quality of life. This episode explains what dystonia is, why it frequently appears alongside Parkinson’s, and what therapies - from medications to DBS to physical therapy – are helping people regain control. So, listen on as a movement disorder specialist, Dr. Niemann, breaks down dystonia. He helps us understand symptoms, treatment options and everyday strategies for living your best life with dystonia. Thank you to our sponsor – Boston Scientific, the maker of...
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125 From Vision to Impact: Growing a Parkinson's Wellness Network
The Parkinson's Experience podcast
This year I have been highlighting some of local areas in the U.S. where people with Parkinson’s take classes designed for their needs, provide social support, and community. It is truly magical to have this kind of central location just focused on your needs as a person with Parkinson’s. If this exist in your area, like Power for Parkinson’s in Austin and my guest today from Parkinson’s Body & Mind in Connecticut, please take advantage of it. Exercise is the only proven way to slow the progression of the disease. Let’s exercise and build a community together. Lynn...
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124 Magic with a Parkinson's Sleight of Hand
The Parkinson's Experience podcast
Who doesn’t like magic tricks? I love watching magicians trying to surprise the audience with their slight of hand tricks. Always fascinates me and asking how do they do that. What does this have to do with the Parkinson’s Experience? Well, my guest today turned to learning magic after he was diagnosed with PD and could no longer work as a nurse. Although his main symptom is bradykinesia or slowness of movement, he is able to perform magic with a little help from getting Deep Brain Stimulation surgery. He performs and has recruited a community of magicians to join him is raising awareness...
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123 Fall Prevention and Safety
The Parkinson's Experience podcast
September is Fall Prevention month. As we age, falling—or even the fear of falling—becomes increasingly common. For people with Parkinson’s, the risk is often higher due to specific changes in the body that affect balance, strength, and coordination. Almost all of us will experience a fall at some point, which is why it’s so important to understand your abilities, recognize your tendencies, and keep open communication with your neurologist and care team. The good news is that there are effective ways to improve balance, manage dizziness, and build strength. Prevention truly is key....
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122 PPMI - How You Can Help Find a Cure
The Parkinson's Experience podcast
I’ve been eager to share with all of you in podcast land some important information and history about what I believe is one of the key drivers in helping fulfill the Michael J. Fox Foundation’s mission to cure Parkinson’s disease. The Parkinson’s Progression Markers Initiative (PPMI), launched in 2010, is a groundbreaking study involving people both with and without Parkinson’s. It gathers data over time to help researchers better understand how Parkinson’s starts, how it progresses, and — most importantly — how to stop it. Sound important? It absolutely is. And it’s still...
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121 Thriving with Parkinson's
The Parkinson's Experience podcast
Listening to personal Parkinson’s stories offers valuable insights for everyone. In this episode, we interview Greg Ritscher, who responded to his diagnosis with determination shaped by his business and personal experiences. Greg also shares a notable DBS story. His journey highlights motivation, positivity, community support, and advocacy. Enjoy our inspiring conversation with Greg. Thank you to our sponsor – Boston Scientific, the maker of Vercise Genus, a Deep Brain Stimulation or DBS system. To learn more about the latest treatment options for Parkinson’s disease at...
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120 Vestibular Therapy - Your Inner Ear and You
The Parkinson's Experience podcast
The range of symptoms and affected body systems in Parkinson’s disease is extensive. One area that is less frequently discussed is the vestibular system—the inner ear structure directly connected to the brain, responsible for balance and spatial orientation. When this system malfunctions, individuals may experience dizziness, balance problems and an increased risk of falls, highlighting its importance in your overall health. With aging, the inner ear naturally becomes less robust. Although current research has not yet identified a definitive cause for the higher incidence of vestibular...
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119 Driving Advice for Parkinson's
The Parkinson's Experience podcast
One of the possibilities along the Parkinson’s journey is losing the ability to drive safely. This possibility is a scary one. For many, driving equals independence. So, it means more than just the hassle of getting around. It means losing your independence. It can lead to depression and anxiety. However, it is important to be safe on the road while driving a multi-ton vehicle. We must protect ourselves, our family, and others on the road. So, we are talking today with an Occupational Therapist who is so passionate about this topic that she started a business focused on helping people keep...
info_outlineAs we wind down the year with a final couple of episodes, this may be the most important topic. November is caregivers’ awareness month. The Caregiver Action Network (CAN) mission is to promote resourcefulness and respect for tens of millions of family caregivers across the country. This not-for-profit organization is responsible for caregivers’ awareness month. It is vital that we recognize this important person in our lives. They are the unsung heroes in our journey with Parkinson’s or any other chronic disease. They are often overworked, overlooked, and overwhelmed. These important people are part of the care team and should have access to the resources and assistance they deserve.
So, let’s get some insight into the care giving from a couple of real-life caregivers who care for their partners with Parkinson’s. Each has a different situation determined by the progression of the disease, current working status as well as other factors.
This episode is for everyone. You never know when you might become a caregiver for a loved one. 17 Branches and the Parkinson’s Experience recognizes and appreciates all of you who care for your partners and your family.
Happy Thanksgiving. I am grateful for all the people who listen to the Parkinson’s Experience podcast.
https://www.dbsandme.com/en.html
https://www.caregiveraction.org/
https://www.parkinson.org/library/fact-sheets/coping-care-partners