Get out and move with your community! Every dollar raised supports the Parkinson’s Foundation mission to make life better for people affected by Parkinson’s disease (PD). At Moving Day Community Walks across the country, we’re fighting Parkinson’s and celebrating movement — proven to help manage Parkinson’s symptoms — and we’re doing it together. The Moving Day Community Walk Program is a complement to the Parkinson’s Foundation Moving Day, A Walk for Parkinson’s. These walks are family-friendly and help the Foundation make life better for people with PD.
The Community Walk program offers volunteers an opportunity to organize a walk in their own community that does not have a Moving Day event. The program leverages the personal experiences and community leadership of passionate volunteers to promote Parkinson’s awareness and raise funds for the Parkinson’s Foundation.
The Parkinson's Foundation Hospital Care Partner Workshop
9:30 am to 12:00 pm CDT
FREE
Early Check-in and resource tables open at 9 a.m. CST.
Presentation and speakers begin at 10 a.m CST.
The Parkinson's Foundation Tennessee & Kentucky Chapter and the Murfreesboro TN Support Group is pleased to host the Parkinson's Foundation Hospital Care Partner Workshop. The workshop will take People with Parkinson's, Care Partners, Support Group leaders and the community through the step-by-step process on how to use the new Parkinson's Foundation Hospital Safety Guide.
There is no charge to attend, but registration is required. This program is open to people with Parkinson's, their family, friends, and the community.
COVID SAFETY: The health and safety of our participants, sponsors, volunteers and staff are our top priority. We continue to monitor CDC recommendations and will adhere to state and local COVID guidelines in place on the event day. Adjustments will be made if necessary.
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In-person check-in starts at 12:30 p.m.
Emotional and social health is an important part of living well with Parkinson’s disease (PD). Many symptoms of Parkinson’s can affect emotional and social wellness. Learn how various clinical and creative therapies can support not only symptom management but the overall well-being of the person living with PD.
Speakers
Jaimie Barr
UM Udall Center of Excellence for Parkinson's Disease Research
Roger Albin, MD
Director
UM Udall Center of Excellence for Parkinson's Disease Research
University of Michigan Health, a Parkinson's Foundation Center of Excellence
Taylor Schmitt, PhD
University of Michigan Health, a Parkinson's Foundation Center of Excellence
There is no charge to attend, but registration is required. This program is open to people with Parkinson's, their family, friends and the community.
The Parkinson’s Foundation Great Lakes Chapter is pleased to be working with Michigan Medicine for the March 15th and June 21st programs in Ann Arbor, Michigan.
COVID SAFETY: The health and safety of our participants, sponsors, volunteers and staff are our top priority. We continue to monitor CDC recommendations and will adhere to state and local COVID guidelines in place on the event day. Adjustments will be made if necessary.
Parkinson’s Revolution will take place across the country on February 24, 2024. Join us in-person at your studio location or virtually for a high energy ride that generates funds and awareness for Parkinson’s disease (PD).
Come ride for a reason and then celebrate the power of movement at our post-ride happy hour the Sweat Social! Friends, family, and members of the PD community are welcome to enjoy a short program and light refreshments immediately following the ride.
A good night’s sleep is critical to our health and well-being. For people with Parkinson’s, sleep is more important as the brain and body need more time to restore. Learn about the common sleep issues associated with Parkinson's disease, how it affects sleep quality, and explore ways to get a better night's sleep while living with PD.
Parkinson's Journey in Color: Advancing Research and Care
10:00 am to 1:00 pm EST
FREE
Parkinson's Journey in Color: Advancing Research and Care in Your Community
Join us for a community day where you can:
– Get resources to help you navigate every stage of Parkinson's disease
– Learn about Parkinson's research and our genetics study, PD GENEration: Mapping the Future of Parkinson's Disease
– Meet Parkinson's Foundation Research Advocates and hear their Parkinson's journey
Enjoy a complimentary lunch and a facilitated movement break!
This event is free to attend, open to all in the community, and centered on the experiences of Black and African American people affected by Parkinson's disease.
COVID SAFETY: The health and safety of our participants, sponsors, volunteers and staff are our top priority. We continue to monitor CDC recommendations and will adhere to state and local COVID guidelines in place on the event day. Adjustments will be made if necessary.
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In-person check in starts at 11 a.m.; Program starts 11:30 a.m.
Studies have demonstrated that exercise has brain and body benefits for people with Parkinson’s disease. Exercise can help to improve Parkinson’s symptoms and help individuals do the activities they enjoy. Learn that there are benefits to movement at all stages of Parkinson’s and that it is never too late to start.
Speakers
Jim Christoffel, PT, DPT, NCS
Miami Valley Hospital
Jackie Magary, PT, DPT, NCS
Kettering Health Network
Tyler McLean, PT, DPT
Kettering Health Network
This program is free and is open to individuals with Parkinson’s, their loved ones, and the community. There is no charge to attend, but registration is required as in-person seating is limited.
Join us directly after our "Fitness Counts" program for our Dayton Resource Fair! Adjacent to the educational program space from 1:30 p.m. to 2:30 p.m., we will have local Parkinson’s resources lined up to hand out free information and resources. There will also be music, food trucks, and fun for your entire support team!
COVID SAFETY: The health and safety of our participants, sponsors, volunteers and staff are our top priority. We continue to monitor CDC recommendations and will adhere to state and local COVID guidelines in place on the event day. Adjustments will be made if necessary.
In-person check-in and vendor visits start at 9 a.m.
APDA Minnesota Chapter, Parkinson's Foundation, and the Udall Center at the University of Minnesota are the three leading organizations for Parkinson's disease advocacy in Minnesota. We are excited to invite you to the annual Spring Parkinson's Symposium.
We will cover mood changes, cognitive changes, and research updates on Parkinson's disease. Attend in-person or online.
Note: We are currently at capacity for our in-person attendance. We hope you can register to join us virtually via Zoom.
For in-person attendees: In-person check-in and vendor visits start at 9 a.m.
For virtual attendees, via Zoom: The live stream starts at 10 a.m.
There is no charge to attend, but registration is required. This program is open to people with Parkinson's, their family, friends and the community.
COVID SAFETY: The health and safety of our participants, sponsors, volunteers and staff are our top priority. We continue to monitor CDC recommendations and will adhere to state and local COVID guidelines in place on the event day. Adjustments will be made if necessary.
In 2021, I received a weekly newsletter email from the local spin studio I’m a regular at in Sacramento, CA. The email was promoting the first Parkinson’s Revolution that would be held in just a few months. My grandfather (who we call “Papa”) was diagnosed with Parkinson’s disease (PD) about 10 years prior. I immediately clicked the link to sign up because I had to support this cause that I had a close connection with.
Once I signed up and learned that I could also fundraise for the event, I thought “hey, why not?!” and I started bugging family and friends to donate. Ride day arrived and I was eager to participate and maybe connect with other people who were indirectly affected by Parkinson’s in the way that I was. As I approached the check-in table, I was greeted with welcoming smiles from the lead volunteer and Parkinson’s Foundation staff who hyped me up for being the top fundraiser! I was so excited. Once the event was over, Foundation staff asked if I would be interested in volunteering and almost four years later… I’m still here!
My Papa is a retired fire captain, was an avid golfer, enjoyed running marathons and could build just about anything before his battle with PD. He is the strongest and most humble man I know. When he was diagnosed with PD, I didn’t understand what was ahead of us as a family. I never really knew what Parkinson’s was. Through his battle with the disease, we’ve watched him lose his ability to do the things he loves.
Volunteering for the Parkinson’s Foundation has not only been rewarding, but also humbling and cathartic for me. During my time as a volunteer, I have been so lucky to meet other amazing volunteers who do not let their diagnosis get in their way from achieving anything and everything they want. I’ve met other family members of people with Parkinson’s who understand the heartbreak of watching your loved ones lose the ability to do the things they love as they age in their battle.
The connections I have made through the Parkinson’s Foundation have taught me what perseverance, strength and support really mean. I am so grateful to my fellow committee members, event participants and Foundation staff for being the community I never knew I needed.
The resources the Parkinson’s Foundation provides are just as important to caregivers and family members as they are to those living with the disease. My Papa is a pillar in my support system and saved so many lives in his career, and so my volunteer work through the Foundation is the best way I can honor him.
The Parkinson’s Foundation has created a community that is unmatched, and I am so thankful to be a part of it and to keep fighting for those who can’t always fight for themselves.
If you would like to be placed on the in-person waitlist please email Derek at drussell@parkinson.org.
If you would like to participate virtually, please click the orange "Register for Virtual" button above.
Living with Parkinson’s can be challenging, but there are many things you can do to maintain and improve your quality of life. This program will provide you with information to help you find the balance between a proactive approach and wondering what lies ahead.
Speakers
Sarah A Dodwell, MD
MaineHealth
Michael S Kleinman, DO
MaineHealth
Michele Delisle
Occupational Therapist, Back In Motion Physical Therapy
Aimee Reilly, LCSW
Behavioral Health Clinician III at MMP Neurology
Roople Unia, MD
MaineHealth
Anne W Herrick, ANPBC
MaineHealth
There is no charge to attend, but registration is required. This program is open to people with Parkinson's, their family, friends and the community.
Lunch will be provided for in-person registrants. In-person registration is at capacity.
COVID SAFETY: The health and safety of our participants, sponsors, volunteers and staff are our top priority. We continue to monitor CDC recommendations and will adhere to state and local COVID guidelines in place on the event day. Adjustments will be made if necessary.