Episode 32- Accessible Air Travel and Advocacy Updates
Thursday, August 10, 2023
In this Quest Podcast episode, we chat with Mark Fisher, MDA’s Director of Advocacy Engagement and Michael Lewis, MDA’s Director of Disability Policy, an advocate who lives with physical disabilities. They join us to share the most recent air travel updates, advocacy information, and expertise and advise about MDA’s grassroots program and advocacy volunteer efforts. Please join us and make your voices heard about making air travel accessible at mda.org/airtravel.
Your Guests
Michael Lewis

Michael Lewis has spent over a decade working in disability rights for various organizations. His passion for disability policy advocacy stems from his experience as an individual with cerebral palsy. As Director, Disability Policy at MDA, Michael leads MDA’s advocacy efforts on Capitol Hill and with federal agencies to defend and expand access to civil rights, education, economic independence and employment, and accessible recreation and travel for people with neuromuscular diseases and other disabilities. A graduate of UNC-Chapel Hill and Regent University, Michael resides in northern Virginia with his wife and four children.
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 our Advocacy Efforts – https://www.mda.org/get-involved/advocacy
- Join the Grassroots Advocacy Team – https://www.votervoice.net/MDA/register
Host: Mindy Henderson

Mindy Henderson is the Senior Director & 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 a writer, 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 49- Navigating Romance with MDA Ambassadors
In this episode of Quest Podcast, we chat with three of our MDA Ambassadors. Nora…

Episode 48- Living with Intention and Creating a More Beautiful Life
In this Quest Podcast episode, we chat with a certified Life Coach who lives with…

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.,…