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“Parkinson’s and Exercise: Your Questions Answered” – Webinar notes

October 2, 2026 By Parkinson's Community Help

Woman on exercise bike
source: Magnific

In mid-August 2026, the Davis Phinney Foundation hosted a webinar on the importance of exercise for those with Parkinson’s disease (PD). Dr. Jay Alberts and Dr. Daniel Corcos explained that strenuous exercise is strongly encouraged because research shows it may slow the progression of PD. They gave guidelines for what intensity and frequency of exercise impart this effect, and suggested what exercises to focus on if you have limited time, energy, and/or mobility.

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Filed Under: Webinars - Announcements & Notes

“Strategies for Communicating Effectively with Your Doctor [about PD]” – Webinar Notes

September 21, 2026 By Parkinson's Community Help

Doctor and patient
source: Magnific

In July 2026, the American Parkinson’s Disease Association (APDA) hosted a webinar on strategies for communicating effectively with your doctors, for those with Parkinson’s disease (PD) and their care partners. Occupational therapist Sydney Settle discussed how to prepare for your appointments so you can make the most of your limited time with your doctor. Her advice was focused on talking with the neurologist, as the center of the care team for managing PD, but these strategies are useful for talking with healthcare professionals of any specialty.

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Filed Under: Webinars - Announcements & Notes

Register Now for Three-Part APDA Series, “Understanding the Science Behind PD Clinical Trials”

September 9, 2026 By Parkinson's Community Help

Understanding the Science Behind PD Clinical Trials

You don’t need a PhD in biochemistry to understand the exciting developments in Parkinson’s disease (PD) research. This special series by the American Parkinson Disease Association (APDA) makes PD research and clinical trials accessible—no scientific expertise required. The APDA’s Dr. Rebecca Gilbert along with Dr. Kevin McFarthing—a biochemist, PD clinical-trials expert, and person with PD—will present a three-part series, “Understanding the Science Behind PD Clinical Trials.”  The dates are Sept. 23, Oct. 14, and Nov. 12.  Register for all three today. 

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Filed Under: Webinars - Announcements & Notes

“DBS, Focused Ultrasound & Stereotactic Radiotherapy for PD” – Webinar Notes

September 7, 2026 By Parkinson's Community Help

Deep Brain Stimulation Graphic
source; Magnific

In July 2026, the American Parkinson Disease Association (APDA) hosted a webinar on three treatments for Parkinson’s disease (PD): deep brain stimulation (DBS), focused ultrasound (FUS), and stereotactic radiotherapy (SRT). Three different neurosurgeons discussed the three treatments. They shared basic definitions of each procedure, pros and cons, and who might be a good candidate for each procedure.  The webinar was part of the APDA’s “Dr. Gilbert Hosts” series.

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Filed Under: Webinars - Announcements & Notes

“Balance and Parkinson’s with Dr. Nate Coomer” – Webinar Notes

September 4, 2026 By Parkinson's Community Help

source: Magnific

In July 2026, the Northwest Parkinson’s Foundation (NWPF) hosted a webinar on how balance is affected by Parkinson’s disease (PD). Dr. Nate Coomer, a physical therapist who works daily with those with neurological conditions, discussed why people with PD are at higher risk for falls than those of similar age. He described what physical and environmental factors contribute to falls for people with PD, and shared strategies physical therapists use to help people with challenges such as freezing of gait and poor proprioception. He also reviewed some exercises that can be used at home to practice improving one’s balance.

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Filed Under: Webinars - Announcements & Notes

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Stanford Parkinson’s Community Outreach provides vital resources and support to individuals living with Parkinson’s disease (PD), caregivers, family members, and friends. We curate a comprehensive list of PD-related webinars and virtual meetings, sharing insightful summaries through our blog and dedicated email lists.

Whether you seek online support groups, educational webinars, or access to helpful blogs and podcasts, we are here to empower you with the knowledge and connection you need on your Parkinson’s journey.

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