

Having a network of health care professionals, loved ones and community members as part of a care team has shown to improve the quality of life for those living with Parkinson’s disease (PD) and their loved ones. Tune into audio from this Third Thursdays Webinar to listen to our panel of experts discuss how to make the most of your appointments, find specialists and coordinate care to best support the person living with the disease.
If you’d rather listen on the go, subscribe to The Michael J. Fox Foundation’s Parkinson’s Podcast on iTunes or your preferred podcast app. If you enjoyed what you heard, share it with a friend or leave a review! It helps listeners like you find and support our mission.
In this episode, Larry Gifford, a member of The Michael J. Fox Foundation’s Patient Council and co-founder of PD Avengers, who was diagnosed with PD in 2017, speaks with:
- Christie and Prentis Brooks. Christie was diagnosed with Parkinson’s disease in 2013 and lives in Arizona with her husband and care partner Prentis.
- Rachel Dolhun, MD, DipABLM, a movement disorder specialist, a lifestyle physician and the principal medical advisor at MJFF.
- Cristina Colon-Semenza, PhD, PT, a physical therapist and assistant professor of kinesiology at the University of Connecticut.
- Jessica Galgano, PhD, CCC-SLP, a speech language pathologist and co-founder of Open Lines Speech and Communication.
View a transcript of this podcast.
Attend an in-person Parkinson’s IQ + You event near you.
Whether you have Parkinson’s or not, you can help move research forward. Join the study that’s changing everything.