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Real Talk from Patients
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Education & Inspiration

Real Talk from Patients

Members of The Michael J. Fox Foundation community share their experiences with Parkinson's.
  • Six Misconceptions about Parkinson's Support Groups

    Six Misconceptions about Parkinson's Support Groups

    Members of the Parkinson's community shared how their expectations were challenged when they joined a support group.
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  • The Many Masks of Parkinson's

    The Many Masks of Parkinson's

    Guest blogger Cheryl Kingston explores the literal and symbolic masks of Parkinson's disease.
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  • Giving Back and Giving Thanks at the Holidays

    Giving Back and Giving Thanks at the Holidays

    After being diagnosed with young-onset Parkinson's disease, Dan Kinel has become a champion for fueling research and has inspired family and his company to do the same.
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  • Giving for a Cure within Our Lifetimes

    Giving for a Cure within Our Lifetimes

    The life and journey of one man living with Parkinson's inspired his family's powerful commitment to accelerating research toward a cure and enhancing quality of life.
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  • Meet the Foundation's Patient Council

    Meet the Foundation's Patient Council

    Meet MJFF's Patient Council, who help infuse the patient voice into the Foundation's research priorities and outreach to the PD community. And see their latest venture fundraising for a…
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  • 26.2 with Parkinson's: Two MJFF Board Members on Running the NYC Marathon

    26.2 with Parkinson's: Two MJFF Board Members on Running the NYC Marathon

    In advance of this weekend's TCS New York City Marathon, two Foundation Board members chat about taking on this athletic challenge while living with Parkinson's disease and fundraising with…
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  • "We will open doors that were previously closed"

    "We will open doors that were previously closed"

    A member of the newly formed MJFF Public Policy Council, Monnie Lindsay, JD talks about her policy work with the Parkinson's disease community.
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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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