The Organization

MDA is a voluntary health agency founded in 1950 by adults with neuromuscular diseases and parents of children with these disorders. A fundraising organization recognized by the American Medical Association "for significant and lasting contributions to the health and welfare of humanity," MDA is working to defeat muscle-wasting diseases through programs of worldwide research, comprehensive services, professional and public health education, and advocacy.

Clinics

At facilities in MDA’s nationwide network of clinics, individuals receive diagnostic and follow-up care from specialists in muscle disease. In conjunction with this medical care, MDA — through some 145 chapters in the United States and Puerto Rico — provides many other direct services, including assistance with the purchase and repair of wheelchairs, leg braces and communication devices, as well as support groups and summer camps for youngsters.

Research

MDA supports more research on muscle-wasting diseases than any other private-sector organization in the world. MDA-funded scientists are at the forefront of cell-based therapy research and testing potential treatments for several neuromuscular disorders.

Education

MDA conducts far-reaching educational programs for the public and medical professionals, including producing and distributing a wide variety of print and audiovisual materials, and maintaining three Web sites. To increase knowledge of neuromuscular disease among medical professionals, MDA sponsors scientific symposia and other professional meetings.

Advocacy

MDA's advocacy efforts are committed to making life better for people with muscular dystrophy and related muscle diseases by providing representation in matters of public policy and research advancement, nationally and internationally; and facilitating active involvement in these areas by the people it serves.

Funding

MDA’s programs are funded almost entirely by the voluntary contributions of concerned individuals and cooperating organizations.