For 25 years, The Michael J. Fox Foundation has helped fill a critical void in Parkinson’s research — turning early ambition into real, measurable impact.
Our latest short film, written and directed by Nelle Fortenberry, Michael J. Fox's producing partner and MJFF Board member, highlights the work that has advanced our patient-centered mission and the growing momentum driving what comes next. Narrated by MJFF’s Co-Founder and CEO Debi Brooks, the film reflects on MJFF’s journey and the progress that continues to define our role in the field.
📹 Watch the full video at the link in bio.
Yesterday, we gathered in New York City for The Michael J. Fox Foundation’s first-ever Social Influencer Summit, bringing together a group of Parkinson’s creators who are reshaping how the disease is understood and discussed online.
The day created space for connection, learning and thoughtful conversation about the power of social media to build community, raise awareness and drive impact.
Together, attendees explored practical strategies for growing their platforms while staying authentic to who they are and more driven than ever to end Parkinson’s. Sessions focused on storytelling and content creation to science communication and community engagement.
We’re incredibly grateful to everyone who joined us, and all those who continue to use their platforms to raise awareness for Parkinson’s.
Honored to join the first-ever Social Influencer Summit at The Michael J. Fox Foundation @michaeljfoxorg headquarters in NYC today — alongside an incredible community of creators, advocates, and the legendary Michael J. Fox @realmikejfox himself.
The day created space for connection, learning, and thoughtful conversation about the power of social media to build community, raise awareness, and drive real impact.
Seeing everyone come together with so much passion, purpose, and heart reminds me of just how powerful we are when we unite for a cause. God is so good, and I am leaving today feeling incredibly inspired, refueled, and ready to keep pushing forward! ✨🙌🏽
Thank you to @michaeljfoxorg for having me, and to everyone who shared their stories today. Let’s keep using our voices to change the world! 💪🏽
This week, Vermont lawmakers passed bipartisan legislation to ban paraquat — and with the Governor’s signature, Vermont will become the first state in the U.S. to address this environmental risk linked to Parkinson’s disease.
Every step of the way, advocates raised their voices, shared their experiences and pushed for change — and it resulted in a major victory for the Parkinson’s community.
Vermont’s actions send a clear and critical message to other states and our federal government: the time to ban paraquat is now.
Read more in our latest article about this historic milestone and how you can bring this change to your state. Link in bio.
“I can’t get a good night’s sleep.” Is this part of your Parkinson’s experience? If so, you’re far from alone.
Sleep changes are common in Parkinson’s, and researchers are studying new ways to help. Watch this video for three novel approaches that may support more restful nights.
For more on sleep and Parkinson’s — including circadian rhythm, melatonin, sleep medications and more — visit the link in bio.
What questions do you have about sleep and Parkinson’s? Comment below.
Together, we’re powering Parkinson’s progress. Thank you.
Every gift, every voice and every effort — this past April, and every day — adds to the collective impact of our community. Your support is advancing research and proving that together, we are stronger.
Thank you for your support during Parkinson's Awareness Month.
“Many care partners struggle silently and don’t reach out for help,” says Prentis Brooks, who cares for his wife, Christie, who lives with Parkinson’s and multiple system atrophy.
“The isolation of the disease for the care partner – especially in later stages – is something I didn’t expect.
I’ve built a support team of former coworkers, friends and family members, many who have been care partners themselves. We talk regularly. That support has been critical for me.”
This #MentalHealthAwarenessMonth, we’re highlighting the role connection plays for people living with Parkinson’s and their loved ones.
Download our guide for care partners at the link in bio.
Our Virtual Run/Walk returns June 19–21. Join us from anywhere: your neighborhood, your treadmill or even your favorite walking trail. However you choose to move, you’re helping bring us closer to breakthroughs in Parkinson’s research.
Get involved:
✔️ Register at the link in our bio
✔️ Invite friends and family
✔️ Fundraise to amplify your impact
✔️ Track your progress in our Strava club
Every step counts. Sign up today at the link in bio.
Loss of smell is easy to brush off, but it can be an early sign of Parkinson’s risk.
Researchers at @michaeljfoxorg are working to better understand this connection, which could lead to earlier diagnosis, better treatments and ultimately prevention.
People with and without Parkinson’s age 40+ can help by taking a free scratch-and-sniff test at home. Request yours at mysmelltest.org/getmytest. #ParkinsonsAwarenessMonth #parents #parkinsons #foxfoundation
Today’s House vote was a critical win for public health and the Parkinson’s community. By passing the Luna Amendment, Congress removed harmful language from the Farm Bill that could have blocked states from adopting stronger pesticide protections — including efforts to ban dangerous herbicides like paraquat. We’re grateful to @RepLuna and all who voted to protect the public good.
Everyone has a role in ending Parkinson’s.
The actions we take today to lift each other up, exchange ideas and stay engaged move research forward and bring better treatments within reach.
Today is the last day of Parkinson’s Awareness Month. Join us in speeding critical research for patients and families everywhere.
Donate now at our fundraiser or visit the link in bio.
In just a few decades, the Parkinson’s research landscape has transformed — from one limited treatment to a growing pipeline of real possibilities.
Today, new therapies are advancing into clinical trials, bringing us closer to what patients have been waiting for.
Give before April ends to help turn these possibilities into progress. Donate to our fundraiser or visit the link in bio.
