Scott Rider on Living with Parkinson’s Disease – WCBE 90.5 FM

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• Brian Grant Interview (with Scott Rider) March 7, 2019 The Brian Grant Foundation is a great resource for information on exercise for Parkinson's Disease: https://briangrant.org/exercise/ Brian Grant had an impressive 12-year career in the NBA before being diagnosed with Parkinson's. Fellow PDer Scott Rider has a great video interview with Brian, where they talk about the BG Foundation, and life with PD, especially earlier onset PD. https://youtu.be/TJXLUV1LBeI Scott is…
• March 9, 2019 - Parkinson's Weekly Update March 9, 2019 This is a recap of the most interesting news and discussions relating to Parkinson’s Disease this past week. Researchers delivered a sobering statistic that if you can survive more than 10 years with Parkinson's, there is a greater than 50% chance of developing dementia...and reminded us that regular exercise is the best intervention to avoid becoming a statistic. Fee-fi-fo-fum, this…
• Parkinson's Disease News - Editor's Picks (Archive 2016.09) October 15, 2016 Newsfeed: PD News PD Research News PD Fitness News PD Boxing News PD Web Articles PD Blogs PD Editor's Picks PD Twitter Newsfeed ‘The Terrorist Inside My Husband’s Brain’: Robin Williams’ Widow Details His Disease – Live ScienceLive Science'The Terrorist Inside My Husband's Brain': Robin Williams' Widow Details His DiseaseLive ScienceBut Robin Williams was not diagnosed with Lewy body disease…
• The road ahead: 2022 January 20, 2022 # # # # The first post at the start of each year on the SoPD website tries to provide an overview of where things are in the search for ‘disease modifying’ therapies for Parkinson’s.  It is an exercise in managing expectations as well as discussing what research events are scheduled for the next year so that we can keep…
• Vermont Couple Shares Strategies on Managing Neurodegenerative Disease March 12, 2020 Like many couples, Joe and Linda Lacroix of Milton, Vermont, spent much of their lives working, raising families, maintaining their home, and planning for the future. Unlike most, however, there was always a dark cloud looming on their horizon — a gene for Huntington’s disease carried by Joe’s mother. Joe Lacroix, 67, outside his home in Milton, Vermont. (Photo by…
• Planning for the What Ifs: Navigating the Future March 30, 2021 Navigating the Future with Advanced Parkinson’s Disease Dr. Gilbert interviews Eleanora Tornatore-Mikesh for her insights on planning for the future with advanced Parkinson’s Today we continue Parkinson’s Disease: Planning for the What Ifs, a special series of posts that discuss the issues of advanced Parkinson’s disease (PD). Additional background about advanced PD and the full introduction to the series is available if you need…
• 5 Misconceptions about Living with Parkinson’s May 29, 2020 Written by Kelsey Phinney Misconception #1: “Every person living with Parkinson’s has the same symptoms.”  My dad, Davis, told me that there’s a common saying in the Parkinson’s community: “When you know one person living with Parkinson’s, you know ONE person living with Parkinson’s.”  Each person with Parkinson’s is on a journey all their own. And while people with Parkinson’s may have…
• Parkinson’s Foundation, VA Join to Help US Veterans Manage Disease May 19, 2020 The Parkinson’s Foundation and the U.S. Department of Veterans Affairs (VA) are collaborating on an effort to improve the health and life quality of veterans with Parkinson’s disease. The two want to provide people who served in the U.S. Armed Forces with better resources and ways to manage Parkinson’s, a disease that affects nearly 1 million people in the country and about 110,000 veterans, half…
• Living With Parkinson’s June 3, 2021 “If you could get up the courage to begin, you have the courage to succeed.” David Viscott “Hope sees the invisible, feels the intangible, and achieves the impossible.” Helen Keller Introduction: Having gone through a major change in strategy to treat my Parkinson’s (see “Treating Parkinson’s with a Dopamine Agonist: The Ropinirole Taper”), I have returned to re-reading some old blog…
• APDA’s Newly Funded 2023 Research Awardees September 13, 2022 On September 8, 2022, APDA announced 27 new research grants for the year ahead. Our grant recipients are working tirelessly to understand the complexities of Parkinson’s disease (PD) to develop new treatments and eventually, a cure. We are honored to support our researcher’s work. We awarded $2.35 million to support cutting-edge PD research for the 2022-2023 year – a 25% increase in…
• Four lessons learned about the Canadian Parkinson’s community on a cross-country bike tour November 4, 2022 Steve Iseman, Mike Loghrin, Darlene Richards-Loghrin, and Jim Redmond, with the invaluable help of their dear friend and fellow Rigid Rider Mike Snitsinger and Jim’s wife Krista, were able to cycle 8000 km from the Pacific to the Atlantic Ocean, zigzagging north and south to meet with countless Canadians impacted by Parkinson’s. When gearing up for a cross-country cycling tour…
• Geoffrey Scott dead: Dynasty and Dark Shadows actor dies from Parkinson's Disease aged 79 - Express March 3, 2021 Geoffrey Scott dead: Dynasty and Dark Shadows actor dies from Parkinson's Disease aged 79  Express
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• Meet the Leaders of The Victory Summit® Virtual Event: How to Live Well with Parkinson’s March 13, 2021 Over the past 15 years, our greatest joy has been getting to know people living with Parkinson’s. They are our greatest teachers, sources of inspiration, and the people we reach out to when we want to hear the real deal. That’s why we’re handing over our next The Victory Summit® Virtual Event to them. Join these speakers and the Foundation on April 2 as we celebrate Parkinson’s Awareness…