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Real Talk from Patients

Members of The Michael J. Fox Foundation community share their experiences with Parkinson's.


  • Man and woman sitting at a table with a laptop

    Managing Finances, Estate Plans and More during Uncertain Times: Part II

    This is Part II of a three-part blog series. Part I featured a list of key legal documents that every adult should have in place, and should review to ensure they meet current needs. In this post, I…
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  • Two people sitting at a table with a laptop.

    Managing Finances, Estate Plans and More during Uncertain Times: Part I

    We are living in extraordinary times: deep social changes, economic uncertainty and the worries and health challenges of the COVID-19 public-health crisis. What steps can people with Parkinson’s…
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  • Susan Mollohan.

    It’s All About Balance: How Yoga Helps Me Stay Balanced with Parkinson’s Disease

    Guest blogger Susan Mollohan practices yoga to help manage her Parkinson's disease symptoms. Follow along as she demonstrates her favorite poses for improving balance and core strength.
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  • A photo of Claudia Revilla at her home.

    Finding Happiness and Distraction: How I’m Spending My Time While Social Distancing

    Learn about what MJFF Patient Council member, Claudia Revilla, is doing while social distancing at home.
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  • Matt Ackerman.

    My Research Journey: Participating for a Better Future

    Matt Ackerman, an MJFF Patient Council member, wanted to make a difference for the millions of others living with Parkinson’s. That’s why he became a clinical research participant.
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  • Doctor-with-patients

    A Privilege to Participate

    Diane Winiarski not only signs up for every research study on Parkinson’s disease that she can, she feels lucky to be able to do it. Here’s why.
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Fundraise for a Cure

Thousands of Team Fox members worldwide are turning their passions and interests into millions in funding for Parkinson's research.

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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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