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Education & Inspiration

Real Talk from Patients

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


  • Allan Cole and his daughters

    Parenting with Parkinson's

    Guest blogger Allan Cole writes about the balance people with Parkinson's face between being the parent you want to be and taking good care of yourself physically and emotionally.

  • Multi generations of the Parikh family gather for dinner

    Securing a Future for Family and Parkinson's Research

    For Shyam and his wife Nalini Parikh, of West New York, New Jersey, a trip to India revealed the symptoms of a disease Shyam was already familiar with. Both his uncle and brother had been living with…

  • Music Mends Minds

    Music Mends Minds Offers Virtual Sing-a-longs to Stay Connected

    A Los Angeles-based nonprofit that creates musical support groups for people with PD and other neurodegenerative diseases is offering free Zoom sessions to stay connected.

  • Allan Cole

    Team Fox Member Allan Cole Writes about Disclosing His Parkinson's Diagnosis

    Guest blogger Allan Cole, PhD, shares his experience disclosing his Parkinson's diagnosis to his family, friends and colleagues.

  • Richard and Mary

    Generous Gift of IRA Starts with Research

    Read more about charitable giving through your retirement account or other ways you can make an impact with planned giving -- including becoming part of our Legacy Circle.

  • Two people sitting at a table with a laptop.

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

    This is the conclusion of a three-part blog series. Part I featured a list of key financial and estate documents that every adult should have in place, and Part II included documents that focused on…

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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 Could Change 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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