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As we embark on a new year, MDA’s commitment to changing public policy and truly empowering the neuromuscular community remains the same. MDA advocates accomplished a lot last year,  and…

In this Quest Podcast episode, we chat with one of Muscular Dystrophy Association’s Ambassadors, Isaac Banks about finding fulfillment in our lives as we skyrocket into 2024. As a certified…

Graphic Designer and MDA Board of Directors member, Matt Plummer Increased awareness, the dedication of advocates, and innovations in research have brought progress to the treatment landscape of rare disease.…

MDA Ambassador Mike Huddleston Mike Huddleston is 60 years old. He is originally from California and now lives in Severn, MD.  Mike was diagnosed with spinal muscular atrophy (SMA) Type…

MDA Advocacy offers many ways to get involved in the advocacy process. Our primary goal is to empower people living with neuromuscular disease to live, work, and play while leading…

MDA National Ambassador Leah Z. Hello friends, As we say goodbye to 2023, we welcome a New Year. I am so excited to see what 2024 has in store! I…

The 2024 MDA Clinical & Scientific Conference is just around the corner. We’re looking forward to you joining us, as we showcase groundbreaking research and clinical accomplishments by dedicated professionals…

Experts recommend asking these nine questions before joining a clinical trial so you know what to expect.

Study Coordinators at CureDuchenne Link® are seeking individuals living with Duchenne or Becker muscular dystrophy (DMD or BMD) or carriers to participate in a noninterventional study. The objective of this study is…

Quest Media is an innovative adaptive lifestyle platform from MDA. With the power of this platform, we foster awareness and empowerment and have important conversations with experts, thought leaders, and…