Muscular Dystrophy Association

Muscular Dystrophy Association (MDA) is a non-profit organization based in the United States that combats muscular dystrophy and diseases of the nervous system and muscular system in general by funding research, providing medical and community services, and educating health professionals and the general public.

History[edit | edit source]

The Muscular Dystrophy Association was founded in 1950 by a group of adults with muscular dystrophy, parents of children with muscular dystrophy and a physician-scientist studying the disorder. The organization was initially known as the Muscular Dystrophy Associations of America (MDAA) before it was renamed to its current name.

Mission[edit | edit source]

The mission of the MDA is to enhance the lives of those affected by neuromuscular disease by funding worldwide research efforts, providing comprehensive healthcare services and support to MDA families nationwide, and rallying communities to fight back through advocacy, fundraising and local engagement.

Research[edit | edit source]

MDA's research program is focused on the discovery of treatments and cures for neuromuscular diseases. The organization funds research projects worldwide that are contributing to the understanding and treatment of these diseases.

Services[edit | edit source]

MDA provides a wide range of services to individuals with neuromuscular diseases and their families. These include medical consultations, equipment assistance, support groups, summer camps for children, and educational programs.

Fundraising[edit | edit source]

MDA's primary fundraising event is the annual Jerry Lewis MDA Labor Day Telethon, which has raised billions of dollars for the organization since its inception in 1966. Other fundraising efforts include the MDA Lock-Up, MDA Muscle Walk, and various local events.