Advocate
Your voice is powerful.
By helping policymakers understand what is fundamentally important to those who know Parkinson's disease intimately, you can shape their decision-making. Contact your elected officials now and tell them how they can use their votes to support Parkinson’s research and care.
Want to stay up-to-date on Parkinson's public policy? Sign up to join our policy network at michaeljfox.org/advocacy.
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Act Now: Ask Congress to Increase Investments in Parkinson's Research
Urge your lawmakers to invest in Parkinson's breakthroughs. -
Tell Congress to Make Prescription Medicines Affordable and Accessible
Urge lawmakers to support a Medicare Part D out-of-pocket cap. -
Tell Your Governor to Prioritize People with Parkinson's
Each state will be deciding its own prioritization of how the COVID-19 vaccine is rolled out. Urge your governor to advocate for people living with Parkinson’s. -
Tell Congress to Protect People with Parkinson’s in Nursing Homes
Urge your lawmakers to pass legislation that supports long-term care facility residents and workers. -
Interested in Parkinson’s Advocacy? We Need Your Help to Take Action.
Share your contact information and we’ll make sure you receive the latest action alerts and policy updates directly to your inbox. -
Act Now: The Economic Burden of Parkinson’s Disease Is $52 Billion
Tell lawmakers how much Parkinson’s disease costs patients, families and the federal government. -
Compose Your Own Message
Share your story with your elected officials. Craft your own message and let your lawmakers know how public policy impacts people living with Parkinson's disease.
Find Your Elected Officials
Enter your address to find the contact information of your U.S. senators and representative.
Want to Get More Involved?
There are many ways to make your voice heard. Download our advocacy toolkit and other educational materials to learn how you can influence public policy.
“Don’t ever be afraid to tell your story, because the more people calling and emailing their members of Congress, the better. Our voices matter.”
Judy Bellenfant
Parkinson’s advocate and care partner
