“Through centering the voices of Black and African American individuals living with Parkinson’s, we are fostering a more inclusive and equitable approach to care, research and support,” said Evelyn Stevens, our senior director of community engagement. Black and African American people living with Parkinson’s disease often face significant health disparities, limiting access care. To bridge this gap, we launched Parkinson’s Journey in Color: Advancing Research and Care in Your Community — events tailored to meet the unique needs and experiences of local Black and African American PD communities. Learn more today for #BlackHistoryMonth:

More people will be diagnosed with Parkinson’s disease in the United States this year than can fit in the stadium hosting today’s Super Bowl. 🏈 The Parkinson’s Foundation is dedicated to making life better for people with PD by improving care and advancing research toward a cure. Help us put resources in the hands of the Parkinson’s community by sharing this post!

RT @PFResearchTeam: 🚨 @ParkinsonDotOrg teamed up with movement disorder specialists to design guidance in Epic to support better care for h…

RT @PFResearchTeam: Check out this new article about personal utility of #Parkinsons genetic testing results from the @ParkinsonDotOrg PD G…

We're excited for next Wednesday's webinar: Staying Connected: Nurturing Closeness Beyond Parkinson's 🩵 The journey of Parkinson’s disease can create physical, emotional, and cognitive challenges that impact relationships, making it difficult to feel close and connected to a loved one. This webinar will explore ways to deepen and maintain emotional bonds, despite these challenges. Register for free:

“I’ve only recently learned that although African Americans are less likely to be diagnosed with Parkinson’s, they are more likely to experience delays in diagnosis,” said Halston. “This is especially true for African American men. Such later stage diagnoses lead to higher mortality rates among African Americans with PD.” 📖 Today for #BlackHistoryMonth, read Halston’s PD Story:

For National Senior Independence Month, we want to highlight our PD Solo Network! This is a virtual network for people living with Parkinson's disease who live alone, by choice or circumstance. 🤝 The purpose of this group is to create a community of support for those living without a care partner. Learn more:

In less than 3 weeks, Parkinson's Revolution is happening nationwide and in D.C. on 2.22.25. 🩵 We want to see the DMV join us in-studio to ride for Parkinson's! No matter why you’re riding – whether it’s for your mother, grandfather, friend or simply because you want to make a difference in the world – Revolution lets you honor your why. 🚴‍♀️ Register today at

The full impact of Parkinson’s disease within the Black community is unknown, largely due to the historical exclusion of Black and African Americans from the healthcare system and research studies. The Parkinson’s Foundation is working to change this by diversifying PD research and care. Learn more about these efforts for Black History Month:

Rebecca Wallings, PhD, is leveraging her Parkinson’s Foundation Launch Award to investigate how aging impairs a type of immune cell outside the brain — and how this impairment impacts the development of Parkinson’s disease. 🔬 Learn more about Dr. Wallings and her research:

If you’ve been looking for a sign to register for a Moving Day Walk near you - this is it! (Literally) 👟 Help us empower people with Parkinson's through vital programs and research:

Studies have shown that 50% of people with Parkinson's disease get their care from a community neurologist, and nearly 30% receive their Parkinson’s care from a primary care clinician. Healthcare professionals ➡️ Find resources tailored to clinicians providing PD care in the community setting by visiting: 🩺 *The Parkinson’s Foundation gratefully acknowledges AbbVie for their support of the Community Neurology Outreach Initiative.*

Did you know that regular exercise, like golf, can help improve balance, flexibility, and overall well-being for people with Parkinson’s disease? Research shows that just 2.5 hours of exercise per week can slow disease progression and boost quality of life!🏌️‍♂️ 🩵 Want to take it a step further? Tee up for Golf Parkinson’s in April and turn your love for golf into support for the Parkinson’s Foundation! Learn more or sign up today at

@ScottBeighton Hi Scott! If you'd like help finding care near you, know you can connect with our free Parkinson's Helpline for referrals: 1-800-4PD-INFO (1-800-473-4636) | Helpline@Parkinson.org |

The Parkinson’s Foundation Newly Diagnosed Guide is designed to help people with Parkinson’s and their loved ones get started on their PD journey, learn more about PD and prepare for a doctor's appointment. 📖 Download or order your free guide:

Check out our latest podcast episodes, where Parkinson’s experts dive into the topics that matter most to you! 🎧 Our podcast, Parkinson's Substantial Matters, is available on Spotify, Apple Podcasts, iHeartRadio and TuneIn. You can also listen at: 🎙️

Parkinson's Revolution is about 3 things: passion, generating community awareness, and advancing our mission toward a cure.🔥 On 2.22.25, riders will raise funds while participating in a high-energy, in-studio (or virtual) indoor cycling class on the same day. 🚲 Join us and register in one of 24 locations across the country at

It’s officially Black History Month! During February and beyond, we’ll be highlighting how Black and African American people diagnosed with Parkinson’s disease have unique experiences and needs when it comes to living with PD. The Parkinson’s Foundation is dedicated to making health care more inclusive and accessible across the PD community. Know that we’re here with resources designed specifically for the Black & African American Parkinson’s community at 🩵 We are #Together4PD.

📢🌴🌟🏃‍♂️ Parkinson's Champions athletes are on course now at the Miami Marathon! Cheer them on as they help make life better for people living with Parkinson's disease around the world at Special thanks to our crew who flew in all the way from Brazil to spread awareness about PD. Let's go Alexandra, Ana, Ana Carolina, Isadora, and Patricia!