The Muscular Dystrophy Association (MDA) is a nonprofit organization dedicated to funding research and providing support for individuals affected by muscular dystrophy and related neuromuscular diseases. Founded in 1950, the MDA aims to improve the quality of life for patients and their families through education, advocacy, and community services. The MDA also organizes events, such as the annual MDA Telethon, to raise funds for research and support programs. They offer resources like support groups, educational materials, and access to specialized care, helping those affected by conditions like Duchenne muscular dystrophy and amyotrophic lateral sclerosis (ALS).