The Michael J. Fox Foundation for Parkinson's Research

23/06/2026

Michael J. Fox has been recognized in Forbes’ 250 list of America's Most Successful Living Immigrants, honoring individuals whose contributions have helped shape the nation across entertainment, philanthropy, business, science and beyond.

Join us in congratulating Michael on this recognition and reflecting on the lasting impact of his decision to use his voice, platform and lived experience with Parkinson's disease to drive change and advance research for millions of families worldwide.

As Michael wrote in a Forbes op-ed, there's "a critical need for creative, even unorthodox, solutions" – a belief that continues to shape efforts to accelerate breakthroughs for people and families living with Parkinson's.

22/06/2026

This Father’s Day, we’re honoring the dads who inspire us to keep accelerating progress toward a future without Parkinson’s.

For Madison Hurwitz Gettes, founder of Team Fox NOLA, that inspiration is her dad, Gary.

"Ten years ago, my life changed with a phone call. My dad called to tell me he had been diagnosed with Parkinson's," says Madison.

"When someone you love is diagnosed with Parkinson’s, fundraising stops being just about supporting a cause. It becomes deeply personal. I’m not just fundraising for research. I’m fighting for my dad — and for all the dads — so that no other daughter has to get the phone call I got."

Read Madison’s story and learn how one daughter turned fear into action, hope and a powerful Team Fox community. https://www.michaeljfox.org/news/meet-madison-hurwitz-gettes-young-professional-leading-team-fox-nola?os_cid=fb-a1bVL000007fIY1

21/06/2026

“Being a parent, like living with Parkinson’s, can be very humbling. My daughter won’t know what I was or what I am not – she will simply know that I’m her father.

Parkinson’s can sometimes feel like a disease of diminishment, but it doesn’t have to be. Some roles, like being a parent, are simply too big to be diminished.” – Bryan Roberts, MJFF Patient Council member

This Father’s Day, we honor and celebrate all the fathers in our community.

19/06/2026

Momentum is building: On June 18, Representatives Anna Paulina Luna and Chellie Pingree introduced the Paraquat Prevention Act. This significant milestone reflects a growing recognition among lawmakers that paraquat poses a public health concern that deserves national attention.

We spoke with Dan Feehan, MJFF’s chief policy and government affairs officer on where efforts to ban paraquat stand, what’s happening at the state and federal levels and how advocacy is helping drive change.

Read more

Momentum is building to ban paraquat nationwide, with a new bill in Congres and Vermont's first-in-the-nation state ban marking major recent progress.

19/06/2026

Constipation is a frequent and troublesome symptom of Parkinson’s disease. It can affect how medication is absorbed and impact daily life.

Tune in to audio from our recent webinar, where experts share tips for preventing and managing constipation and discuss the latest research on the gut-brain connection in Parkinson’s.

Constipation is a frequent and troublesome symptom of Parkinson’s disease (PD). It can affect how medication is absorbed and impact daily life. Tune in to audio from this month’s Third Thursdays Webinar to hear our panel of experts discuss why constipation happens in Parkinson’s. They also cov...

18/06/2026

New research opportunity for people with Parkinson's disease: our landmark study is expanding access to free genetic screening.

By taking part, you'll gain insights into your Parkinson's while contributing to research that may help explain why the disease affects people differently.

What researchers learn could help accelerate progress toward more personalized treatments.

You may qualify for free genetic screening if you have Parkinson's disease and:
✔️ Have a family history of Parkinson's disease
✔️ Are of Ashkenazi Jewish ancestry

These groups are more likely to carry certain genetic variants linked to Parkinson's disease, making their participation especially valuable for research.

Request your free kit today: bit.ly/4fS6LS5

15/06/2026

It was never just about reaching the summit.

"We’re all doing this for something bigger," said Nathan Willis, who lives with Parkinson's and climbed Mount Kilimanjaro with Team Fox last year in Tanzania, Africa.

On that mountain were stories of resilience, love, loss and determination. People climbing for themselves. For the people they love. And, most importantly, for a future without Parkinson’s.

In 2026, we climb again. Join us this fall to scale Mount Whitney in California or trek Patagonia in Argentina. Learn more: https://michaeljfox.org/endurance?os_cid=fb-a1bVL000007ZSog

🎥 Filmed by Nathan Willis

12/06/2026

For 10 years, Lisa Volenec hid her Parkinson’s diagnosis. When she finally shared her story, she found support, connection and a renewed sense of purpose.

Featured on Good Morning America, Lisa is helping others living with Parkinson’s share their stories and connect with one another.

Drawing on her background in storytelling, she founded This is Parkinson’s to elevate patient voices and highlight the diverse, deeply personal experiences of living with the disease.

Today, Lisa is committed to turning her voice into a platform for others, ensuring that every person living with Parkinson’s is not only heard, but impossible to ignore.

11/06/2026

How can you tell if a Parkinson’s clinical trial is right for you? Research advances depend on volunteers, but it’s natural to have questions about how to pick a trial and what participation might mean for you.

Join our upcoming webinar on Thursday, June 18, at 12 p.m. ET. Our expert panel will walk through the process and share what to expect before, during and after a trial. Join us to ask your questions live. Register here: https://bit.ly/4vc3LVE

This webinar is brought to you with support from BlueRock Therapeutics and Genentech.

10/06/2026

Parkinson’s isn’t easy to diagnose — everyone’s symptoms differ based on their individual biology, leading to delays in diagnosis and treatment.

One of our key areas of focus is finding ways to diagnose Parkinson’s disease earlier and more clearly, which could one day lead to more personalized treatments that can improve quality of life.

Listen to our newest podcast episode to learn more. https://bit.ly/4xhvkhy