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Updates from Washington
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Updates from Washington

News from Capitol Hill and statehouses across the country shifts rapidly, so it’s important to stay up to date. Here, you’ll find the latest information on the policies that The Michael J. Fox Foundation and our nationwide network of policy advocates are working on to support the Parkinson's community.

Capitol Hill

The National Parkinson's Project

On July 2, 2024, President Biden signed the National Plan to End Parkinson’s Act into law, establishing the first-ever federal initiative to prevent and cure Parkinson’s disease, treat its symptoms and slow or stop its progression. 

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  • Ask the MD: Living with Parkinson’s Amid the Coronavirus Pandemic

    People with Parkinson’s Need Access to Telehealth

    Congress has introduced important and relevant legislation designed to keep telehealth as a permanent option. Join us in advocating for this legislation.
    Learn more
  • What Does the Government Shutdown Mean for the Parkinson’s Community?

    Congressional Caucus on Parkinson’s Disease Recognizes April as Parkinson’s Awareness Month

    Joint chairs of the Congressional Caucus on Parkinson’s Disease submitted a resolution designating April as Parkinson’s Awareness Month in the United States.
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  • Screenshot from the 2021 Parkinson's Advocacy Awards ceremony

    Parkinson’s Advocacy Awards Presented to Congressional Leaders and Community Members

    The Parkinson’s Advocacy Awards recognize outstanding individuals or groups who advocate on behalf of the Parkinson’s community.
    Learn more
  • Screenshot from the 2021 virtual Parkinson's Policy Forum

    2021 Virtual Parkinson’s Policy Forum Urges More Federal Investment in Parkinson’s Research

    MJFF hosted the virtual Parkinson’s Policy Forum to bring advocates together to ask their members of Congress for increased funding for the Parkinson’s Research Program at the Department of Defense.
    Learn more
  • Common Questions from Our Webinar on Parkinson's Medications

    People with Parkinson’s Need Access to Affordable Prescription Medications

    Members of Congress will soon begin discussing drug pricing legislation, and hearing from those impacted by Parkinson’s disease is a key part of ensuring any legislation reflects the needs of the…
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  • Capitol building in Washington D.C.

    A Meeting with The White House: Our Partners in Research Toward a Parkinson's Cure

    MJFF leadership — including Michael J. Fox, Co-Founder Debi Brooks, CEO Todd Sherer, PhD, and SVP of Public Policy Ted Thompson — met virtually with White House representatives to discuss how robust…
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  • Capitol building in Washington D.C.

    Bringing Parkinson’s Policy Priorities to the New Congress

    On January 3, Representatives and Senators were sworn in for the 117th Congress in the United States.
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Michael J. Fox in blue sweater posing for the camera.

Patients First

Our Foundation exists for one reason: to speed breakthroughs patients can feel in their everyday lives.

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Join the Parkinson's Policy Network

By telling your personal story, you can shape policymakers' decisions on issues of importance to the Parkinson's community.

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