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Webinars

On the third Thursday of every month at 12 p.m. ET, join our free live webinars to learn about various aspects of living with Parkinson's disease and our work to speed medical breakthroughs. Log on, listen to the expert discussion and submit your own questions to our panelists.

And join us for other special free webinars throughout the year (dates and times to be announced) on varied topics of interest to the Parkinson's community.

Third Thursdays Webinars from 2018 and 2019 are available for CME credit for practicing health care professionals for two years from their air date. Register for an on-demand webinar to learn more. We apologize that we are not offering CME credit for webinars from 2020 forward. 


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    What Comes Next? Living with Parkinson’s Years after Diagnosis

    Our expert panelists discuss social, emotional and physical changes you may notice after living with Parkinson’s for some time. We cover tips for managing changes and symptoms and share opportunities…
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    Estate Tax Overhaul: Radical Changes Require Important Planning

    The recently proposed “For the 99.5% Act” would bring sweeping changes to all aspects of estate planning, including the taxation of estates and inherited gains. The “Sensible Taxation and Equity…
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    Deep Brain Stimulation: Is It Right for Me or My Loved One?

    Our experts discuss who should consider deep brain stimulation (DBS), a surgical procedure for Parkinson’s. We cover how the procedure works, what someone may expect after the surgery and the latest…
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    You’re Not Alone: Tips for Building Connections in the Parkinson’s Community

    Our panelists discuss loneliness and isolation that can happen in Parkinson’s disease. We cover ways to manage these issues through community connections and share information on the Parkinson’s…
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    A Conversation with Michael J. Fox: On Testing the Limits of Optimism

    Michael J. Fox sits down with Foundation Co-Founder Debi Brooks to discuss his latest memoir, “No Time Like the Future: An Optimist Considers Mortality.” Join us for this special conversation during…
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    Volunteering for Parkinson’s Research: What to Know and Expect

    Our panelists discuss different types of clinical research and how to find the best study for you. We cover potential benefits and risks of participation and how volunteering for research can become…
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The MJFF webinar series has been made possible through the leadership of members of our Parkinson's Disease Education Consortium in conjunction with The Albert B. Glickman Parkinson's Disease Education Program. These partners' support allows us to furnish high-quality educational content to the Parkinson's community while maintaining our commitment to allocate donor dollars to high-impact research. Editorial control of all Michael J. Fox Foundation-published content rests solely with the Foundation.

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Join the Study that's Changing Everything

The Parkinson's Progression Markers Initiative is changing how patients, families, doctors and scientists think about brain disease. Now it needs you.

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Breaking Research Updates

Read the latest developments in the field’s understanding and treatment of Parkinson’s disease.

Read Research News
What matters most isn't getting diagnosed with Parkinson's; it's what you do next. The choices we make after we're diagnosed can open doors to possibilities you'd never imagine.
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