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The Muscular Dystrophy Association (MDA) is a voluntary health agency - that is a dedicated partnership between scientists and concerned citizens aimed at conquering neuromuscular diseases that affect more than one million Americans.
Started in 1950 by a group of parents whose children had MD, the organization has grown into the world's leading voluntary agency in genetic research and patient services. MDA has over 160 local offices, 230 hospital-affiliated clinic, and 90 summer camps. MDA provides research, services and education for over 43 neuromuscular diseases. All money raised stay local to help those MDA serves in your community.