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MDA is the #1 health nonprofit advancing research, care and advocacy for people living with muscular dystrophy, ALS, and related neuromuscular diseases.
Muscular Dystrophy Association (MDA) is the #1 voluntary health organization in the United States for people living with muscular dystrophy, ALS, and related neuromuscular diseases. For over 70 years, MDA has led the way in accelerating research, advancing care, and advocating for the support of our families.
Muscular Dystrophy Association ( MDA) is an American nonprofit organization dedicated to supporting people living with muscular dystrophy, ALS, and related neuromuscular diseases.
MDA is the #1 health nonprofit advancing research, care and advocacy for people living with muscular dystrophy, ALS, and related neuromuscular diseases.
4 days ago · Quest is the largest adaptive lifestyle content platform for the neuromuscular disease community and the disability community at large. Quest includes MDA's flagship magazine, as well as a blog, newsletter, and podcast.
MDA leads the way in caring for people living with muscular dystrophy, ALS, and related NMDs, with the largest nationwide network of multidisciplinary MDA Care Centers.
Feb 12, 2024 · They can also help you find information on your disease, get started with an MDA Care Center, learn about research and clinical trial opportunities, and direct you to resources and services in your community. Contact the Resource Center at 833-ASK-MDA1 or ResourceCenter@mdausa.org.
Jul 18, 2024 · Summary: A new gene therapy treatment for Duchenne muscular dystrophy (DMD) shows promise of not only arresting the decline of the muscles of those affected by this inherited genetic disease, but ...
As the Muscular Dystrophy Association (MDA) continues our commitment to empowering people living with neuromuscular disease, we are excited to share our 2022 blog series: “Quest for Success”.
Jul 21, 2024 · Duchenne muscular dystrophy (DMD) is a fatal genetic disease afflicting approximately 1 in 3800–6300 live male births and caused by genetic mutations in the DMD gene located on the X chromosome ...
