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
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This webinar will explore what causes ICDs, how to manage them, and practical tools to support those impacted.
Live Fitness Friday - Active and Rising
Get moving with PD-tailored fitness videos that feature a different focus every week, from balance to coordination and more.
Parkinson's Revolution Dallas
Join us in-person at your studio location or virtually for a high energy ride that generates funds and awareness for Parkinson’s disease.