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Raise funds to support research and provide services for area children and adults living with Muscular Dystrophy.
This is the Massachusetts office of the Muscular Dystrophy Association. We raise funds in our state to support the services supplied to local familes living with any of 43 neuromuscular disease covered under MDA including ALS. The funds are earmarked to support a local clinic, local support groups for parents and families of clients with MD, assistance with the repair of wheelchairs, leg braces and communication devices, and a special summer camp for area children and young adults with MD.