The Parkinson’s Foundation makes life better for people with Parkinson’s  disease (PD) by improving care and advancing research toward a cure. In  everything we do, we build on the energy, experience and passion of our  global Parkinson’s community. 

The Michael J. Fox Foundation is dedicated to finding a cure for Parkinson's disease through an aggressively funded research agenda and to ensuring the development of improved therapies for those living with Parkinson's today.

Quality of life is the impetus behind every program and research study the Davis Phinney Foundation funds. 

 The American Parkinson Disease Association works tirelessly every day to  support and empower anyone who is impacted by Parkinson’s disease (PD).  Our nationwide network provides information and referral, education and  support programs, health and wellness activities, and other events to  facilitate a better quality of life for the PD community, while also  funding vital research.

The Brian Grant Foundation empowers people impacted by Parkinson's to lead active and fulfilling lives. We believe in caring for the whole person—mind, body, and spirit—and provide evidence-based resources that support wellness in all facets of life.

 Parkinson’s Foundation Great Lakes makes life better for people with  Parkinson’s disease (PD) by improving care and advancing research  towards a cure. Whether you are newly diagnosed with PD or have been  managing it for years, are a care partner, family member or friend of  someone with PD, they are here to help you.  

Services Support Groups; Exercise & wellness programs; Special Events; Volunteer Opportunities; Education; Exercise programs and support.

 The study objective is to establish the efficacy of high-intensity  endurance exercise as first-line therapy for recently diagnosed people with Parkinson's disease (PD). Preclinical data,  experimental data on humans, and epidemiological data all have demonstrated benefits of endurance  exercise on the motor and nonmotor signs and symptoms of the disease, 

Ongoing clinical and research updates related to new therapies and progress in the research to find a cure. 

Ongoing clinical and research articles related to new therapies and progress in the research to find a cure. 

Every month, Stanford Parkinson’s Community Outreach produces a list of  Parkinson’s-related webinars and virtual meetings with speakers. Here’s  our July 2024 list.

What’s the difference between a webinar and a virtual meeting? A  “webinar” has a handful of speakers at most, and attendees have both  audio and video muted. A “virtual meeting” usually allows attendees to  be seen and heard.

We recommend you register NOW for anything of  interest. That way, if there’s a recording, as a registrant you’ll  receive an email alerting you to the recording availability. Also, note  that a few webinars have registration deadlines well in advance of the  webinar dates.

Stanford Parkinson’s Community Outreach will try  to attend as many of these events as possible and share our notes. Our  notes about PD webinars are often posted to our blog. We email our notes  to the “Stanford PD Info” and “PD Caregivers” email lists, depending on  the relevance to those audiences.

All programs and classes listed below are available online, and you can participate no matter where you live.
Use the check boxes below to filter by type of program and/or by month to narrow your search.
Please take particular note of the time zone listed, as some programs originate in a time zone different than yours.

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Parkinson's Foundation and Northwestern Medicine Parkinson's Disease and Movement Disorders Center present: Parkinson's Disease Patient and Family Symposium.

This program will feature experts discussing: Tips from a Movement  Disorder Specialist, Advances in Parkinson’s Research, and the Benefits  of the Creative Arts for PD. Q&A with the experts, will follow each  presentation.

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