Parkinson & Movement Disorder Alliance

09/04/2026

"Currently in our system, there are approximately 660 movement disorder specialists in the U.S. There's less than 10 in rural areas. And there's over 40 million people with a movement disorder, not just Parkinson's. Even if a doctor was in clinic every single day, that's 60,000-plus patients that they have to see over a year. The math doesn't math."
—Rebecca Korduner, Deputy CEO, PMD Alliance

We're here to listen to everyone in this community—and that means listening to where the gaps are for healthcare providers, patients, care partners, and beyond. Because of this, we've created an innovative therapeutics conference for health providers in movement disorders (ATMRD) and a professional mentoring program (CAMP-FiRE) for the next generation of specialists—all aimed to make sure you get the expert care you need.

Fight the care crisis with a donation today at pmdalliance.org/give

09/03/2026

"I often find in my visit summary, after my appointment, that my doctor has major points recorded wrong. Not what I was conveying, or trying to convey. Frustrating to say the least." —Cindy

09/02/2026

In this powerful documentary called "Redefining Victory," individuals share their personal journeys with Parkinson’s disease, from the first signs and diagnosis to the everyday challenges and triumphs of living with it. Through honest conversations, they reveal how they have learned to adapt, manage symptoms, and focus on living full and meaningful lives. This film is a testament to the strength of the human spirit and a reminder that even in the face of uncertainty, life can still be lived with purpose, joy, and hope.

Watch now: https://loom.ly/JLPVq7U
Greg's Moving Crew

In this powerful documentary, individuals share their personal jour...

09/02/2026

Don't make it weird & more great tips from our friends at The Michael J. Fox Foundation for Parkinson's Research on what to do when your friend tells you they have PD:

What does it mean to be a good friend to someone living with Parkin...

09/01/2026

"PMD Alliance is the only organization that I know in this space that is really working on today's problems to enhance quality of life for Parkinson's patients. And the work that they're doing, the commitment they have, is next to none."
—Ritesh Ramdhani, MD

Dr. Ramdhani, a movement disorder specialist, has been working alongside us as a professional mentor to the next generation of movement disorder providers. Together, we're fueling the pipeline of new specialists to ensure that every person with a movement disorder has access to the high-quality, knowledgeable care they deserve. He's been a part of, and has seen firsthand, the unprecedented way our advanced therapeutics congress (ATMRD) for healthcare providers brings the entire ecosystem together to educate and empower providers.

Donate now to put Parkinson's quality of life first at pmdalliance.org/give.

08/31/2026

Ellen Martin and Cody, her service dog, have been a team for five years. Ellen, who has essential tremors and a gait disorder, is grateful for the way Cody supports her with both mobility and psychiatric tasks. Because of him, she says, she feels less alone.

Catch the full webinar and learn how service dogs from organizations like Atlas Assistance Dogs may be able to help you: https://loom.ly/vsfduKw

08/30/2026

When Sat started sharing his young onset Parkinson's diagnosis with his friends, he noticed two different reactions: people either leaned in and showed up, or they disappeared. The people who disappeared didn't seem to know how to respond to his diagnosis or what to say. "I want to tell them: I'm still Sat," he said. "I'm still the same person."

08/28/2026

"My husband was laid off 6 months before he was thinking of retiring. Then my symptoms went through the roof and I had to go on long-term disability. (I turn 60 this month.) Our income went down about 75%, plus I now pay close to $1,000/month for Cobra—which, as you can imagine, added way more stress. I was the main high income earner. My husband now drives me to appointments as I now get lost and my memory is going and having conversations is hard. He works part-time to supplement. We went from a very comfortable income to this in months. Not prepared at all." —Evie

08/27/2026

When Jorge Patino, MD, a movement fellow at the University of Cincinnati, discovered ATMRD, our innovative therapeutics conference for healthcare providers, it helped him validate that movement disorders was the specialty he wanted to pursue.

From there, he joined CAMP-FiRE, our professional mentorship program for residents and fellows, which introduced him to a whole new world of therapies and research—including how he could get involved in these exciting developments.

The need for more doctors who specialize in movement disorders is critical. There is a huge shortage of specialists and big wait times to get an appointment. For us, ATMRD and CAMP-FiRE are two essential steps to supporting and preparing the next generation of specialists.

08/27/2026

Parkinson’s may change dating, but it doesn’t change what you deserve from love. ♥️

After being diagnosed with young-onset Parkinson’s, Mel found herself navigating dating, disclosure, and all the uncertainty that comes with letting someone new into your life.

What she discovered? A diagnosis doesn’t make you less worthy of chemistry, connection, or being swept off your feet.

In her Guest Column, Mel shares why finding love meant showing up honestly and taking a “calculated risk.”

🔗 Read Mel’s full story here: https://bit.ly/3UBltUU