IP Programs
ALL IN!™ Summit

Building Capacity + Creating Connections in the Movement Disorders Community

Austin, TX • November 20-21

IP Programs
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I Am...

Click where you fall in our ecosystem to get started.

Person with a Movement Disorder

Care Partner or Family Member

Recently Diagnosed

 

 

Support Group Leader

 

 

 

Healthcare Provider

 

 

 

Care Facility

 

Our Mission

We’re an independent, national nonprofit on a mission to empower people impacted by movement disorders with the tools and meaningful connections they need to thrive today. We provide free resources to the entire Movement Disorder Care & Support Ecosystem©—to people living with the disease, care partners and adult children, support group leaders, and healthcare providers—because we all do better when everyone’s empowered.

We believe in expanding access to high quality, expert-driven, deep-diving online and in-person programs, including offering a vast on-demand video library. We create courageous spaces for you to connect with community, cultivate positive change, and spark joy.

We’re here to navigate the waves of a movement disorder together, bringing clarity and life-giving solutions. You are not alone.

“For support group leaders, PMD Alliance is a source of comprehensive and relevant PD information delivered by kind, caring, forward-thinking people. Their information is timely and unique and reflects the needs of their constituents now, making it a wonderful resource for support group leaders committed to the PD community. ”

David MilesSupport Group Leader

“The PMD Alliance is an advocacy force in the PD community. They are unique in that their focus is practical - providing patient education that matters to patients, empowering them to bring that info back to their doctors and be their best advocates. They are unique in that their reach is broad - not just globally with the new virtual world, but they engage doctors and all members of the care team as much as patients, through legislative advocacy efforts, industry partnerships and research.”

Jill FarmerDO, MPH

“Parkinson’s is such a daunting disease, it is easy to be overwhelmed. Mark and I feel so fortunate to have found PMD Alliance who has provided patient and caregiver education, research updates, and exercise and social programs. PMD Alliance has truly been a lifesaver for us.”

Mimi and Mark TiptonLiving with PD

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PMD Alliance expressly prohibits discrimination, harassment and retaliation based on race, color, sexual orientation, religious orientation, physical barrier and HIV status, ancestry, creed, national origin, disability or perceived disability, veteran’s status, age, gender identity or marital status, ethnicity, economic status, educational status or any other protected category.