Muscular Dystrophy Association

The Muscular Dystrophy Association (MDA) is the leading nonprofit organization dedicated to advancing research, care, and advocacy for individuals affected by muscular dystrophy, ALS, and other neuromuscular diseases. Central to MDA’s mission is providing comprehensive support to families and individuals impacted by conditions such as Spinal Muscular Atrophy (SMA), Duchenne Muscular Dystrophy (DMD), and Amyotrophic Lateral Sclerosis (ALS).

MDA offers a range of essential services, including access to specialized care centers, community education resources, and research funding aimed at developing innovative therapies. The organization actively promotes awareness and understanding of neuromuscular diseases through programs like the MDA Gene Therapy Support Network and various educational workshops.

In addition to its advocacy and educational efforts, MDA engages the community through events, volunteer opportunities, and fundraising initiatives, ensuring that every contribution makes a meaningful impact. By fostering connections and delivering vital support, MDA remains committed to improving the lives of those living with neuromuscular conditions.