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Jennifer Cruz and her mother Jennifer Cruz is 36 years old and lives in Broken Arrow, OK. Jennifer has Ullrich congenital muscular dystrophy and uses a wheelchair and noninvasive ventilation.…

Marshall Eckert in the Air Force Marshall Eckert currently resides in Virginia, just outside the capital, and navigates life with Limb-Girdle Muscular Dystrophy Type 2B. He is a proud alumnus…

MDA Summer Camp creates opportunities for youth living with neuromuscular disease to gain confidence, increase communication skills, try new things, tackle challenges, and dream big. It is a truly unique…

The recent FDA approval of Catalyst’s AGAMREE ® (vamorolone) is a beacon of hope for people living with Duchenne muscular dystrophy (DMD), a rare but serious degenerative muscle disease.   According…

Comcast’s Accessibility team is raising the bar when it comes to inclusive design and accessible products and services. With a focus on customer-facing experiences, from remote controls to customer service…

Each year, MDA and Magic Wheelchair team up for a special sweepstakes where one lucky contestant wins an incredible, custom costume that transforms their wheelchair and provides a magical opportunity…

In this Quest Podcast episode, we chat with a distinguished business leader from the St. Louis area, who lives with physical disabilities. Lori Becker, CEO of Starkloff Disability Institute, has…

Tips for family caregivers to recognize the signs of caregiver burnout and manage stress to prevent it.

Happy holidays! The 2023 MDA Quest Media holiday shopping guide is here. Once again, our team of ambassadors have stepped up with their favorite product nominations, not only sharing their…

MDA’s Erin Randall (left) and Jacksonville Fire Station 1, IAFF Local 122 Fire Fighter Chip George (right) pose with Anna on her magical reveal day. A celebration of creativity, inclusion,…