![Podcast: Treating Parkinson's 'Off' Episodes](/sites/default/files/styles/podcast_image/public/images/podcast/Podcast-Image_0.jpg?h=f405c703&itok=W0_J800_)
![Podcast: Treating Parkinson's 'Off' Episodes](/sites/default/files/styles/podcast_image/public/images/podcast/Podcast-Image_0.jpg?h=f405c703&itok=W0_J800_)
The decision-making process around deep brain stimulation (DBS) to treat Parkinson’s motor symptoms can be a complex and emotional journey. People often have questions about when – and whether – to have the procedure and what the experience is like, from the months of evaluation pre-surgery to surgery day to life with the device. In audio from this Third Thursdays Webinar, our panel of people living with Parkinson’s disease (PD) and a movement disorder specialist share their DBS stories and answer audience questions about their choices and experiences.
If you’d rather listen on the go, subscribe to our Michael J. Fox Foundation 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, Team Fox Detroit Founder Donna Rajkovic, who was diagnosed with PD in 2012 and had DBS in 2020, leads a discussion with panelists.
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Ned Neuhaus, who was diagnosed with PD in 2013 and who had DBS in 2022
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Evonne Simoff, who was diagnosed with PD in 2014 and is scheduled for DBS surgery later this year
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Neil Kanta Shetty, MD, a movement disorder specialist at Northwestern Medical Group and assistant professor of neurology at Feinberg School of Medicine
View a transcript of the podcast.
Want to see the slides and other resources from the webinar? Watch on demand.
Learn more about deep brain stimulation and download our free guide on our website.
The Foundation’s landmark study, the Parkinson’s Progression Markers Initiative, also known as PPMI, is recruiting volunteers. Join the study that’s changing everything.