The Muscular Dystrophy Association (MDA) is the nonprofit health agency dedicated to finding treatments and cures for muscular dystrophy, ALS and related diseases by funding worldwide research. The Association also provides comprehensive health care and support services, advocacy and education.
MDA was created in 1950 by a group of adults with muscular dystrophy, parents of children with muscular dystrophy and a physician-scientist studying the disorder.
MDA combats neuromuscular diseases through programs of worldwide research, comprehensive medical and community services, and far-reaching professional and public health education. With national headquarters in Tucson, Ariz., MDA has 120 local offices across the country, sponsors 200 medical clinics and supports some 300 research projects around the world. The Association's programs are funded almost entirely by the voluntary contributions of concerned individuals and cooperating organizations.
Some of MDA's special events and volunteer opportunities include: