Demystifying Parkinson’s Research
We often hear that participating in research is important, but many people have understandable questions and concerns. What happens to my information and data? What’s new in Parkinson’s research? How do I find studies and get involved? Does diversity matter to research?
People with Parkinson’s, their loved ones, and health providers interested in learning more are invited to join the Parkinson’s Foundation for this important talk about common misconceptions and myths about research as well as new research updates.
Speakers
Danielle Larson, MD
Northwestern University Movement Disorders Center, A Parkinson’s Foundation Center of Excellence
Karen Williams, CCRP, Sr. Clinical Research Associate
Northwestern University Movement Disorders Center, 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.
Contact Us
Jessica Bartsch
COVID SAFETY: We’re closely monitoring the coronavirus pandemic and following all local and state regulations for your health and safety. For the safety of the Parkinson’s community, we’re asking our participants to follow city and state guidelines regarding mask usage and social distancing safety protocols. Changes to the event date and location may be made, if necessary. Thank you for doing your part to help protect our community!
Upcoming Events
Community Walk Piedmont Fayette
Moving Day is your chance to speak up about Parkinson’s disease and move others to take action.
Learn More. Live Better. Parkinson's Symposium—Heartland Chapter
Living with Parkinson's can be challenging, but there are many things you can do to maintain and improve your quality of life.
Let's Talk About It
This program will provide strategies for coping and talking about it with healthcare providers or loved ones.