Episode 44- Voting Rights and Accessibility
Thursday, October 3, 2024
In this Quest Podcast episode, we chat with Shaun Hill, MDA’s Manager of Public Policy & Advocacy and Mark Fisher, MDA’s Director of Advocacy Engagement. They join us to share the most recent updates and information about accessible voting, your rights when it comes to accessible voting, and information about MDA’s Access the Vote program and advocacy efforts. Please join us and make your vote count at https://mda.org/vote.
Your Guests
Shaun Hill
Shaun Hill currently serves as Manager, Public Policy & Advocacy for the Muscular Dystrophy Association. Ms. Hill is a veteran government relations professional, who has worked continuously in the healthcare arena, championing causes on behalf of both patients and providers, working through legislative, regulatory, and advocacy channels to impact change. In many of these roles she has led the charge on advocacy campaigns, such as MDA’s current initiative Access the Vote. A native of Washington, DC, she is a graduate of Howard University and has studied political management at George Washington University.
- For Information about voting – https://mda.org/vote
- For local information about voting- https://www.vote.org/
- Join the MDA Grassroots Advocacy Team – https://www.votervoice.net/MDA/register
- Connect with MDA Advocacy –advocacy@mdausa.org
Mark Fisher
Mark Fisher is the Director of Advocacy Engagement at the Muscular Dystrophy Association. In this role, Mark leads MDA’s grassroots program and advocacy volunteer efforts. He works to empower advocates and connect them with key decisionmakers in order to advance public policies that improve the lives of the neuromuscular disease community. He previously served as the Digital Grassroots Manager at the American Heart Association and was also a field organizer on a U.S. Senate campaign. Mark earned his Master of Public Policy from American University and is originally from Pittsburgh, PA.
- For Information about voting – https://mda.org/vote
- For local information about voting- https://www.vote.org/
- Join the MDA Grassroots Advocacy Team – https://www.votervoice.net/MDA/register
- Connect with MDA Advocacy – advocacy@mdausa.org
Host: Mindy Henderson
Mindy Henderson is MDA’s Vice President of Disability Outreach & Empowerment, Editor-in-Chief of Quest Media, and the host of this podcast. She was diagnosed with Spinal Muscular Atrophy, type 2 when she was 15 months old and has been a life-long partner to MDA. Mindy is also a motivational speaker and author of the book, The Truth About Things That Suck.
Connect with Mindy:
Disclaimer: No content on this site should ever be used as a substitute for direct medical advice from your doctor or other qualified clinician.
Listen to this next
Episode 47- Wrapping Up 2024 with Leah and Ira
In this Quest Podcast episode, we chat with Muscular Dystrophy Association’s National Ambassadors, Leah Z.,…
Episode 46- Creating Beauty from your Dreams with Shakiira Rahaman
In this Quest Podcast episode, we chat with the Kira Cosmetics founder and entrepreneur, Shakiira…
Episode 45- Making Space and Creating Pathways with Keely Cat-Wells
In this Quest Podcast episode, we chat with world-renowned advocate, entrepreneur, public speaker and educator,…