Provides public information regarding Muscular Dystrophy and related diseases (such as Lou Gehrig's), including speakers, videos, electronic educational materials, and seminars.

Provides one-on-one support via phone or email for individuals and families looking for an overview of disease information in our program, resources, activities, and more.

Provides virtual peer support groups for individuals affected by neuromuscular disease, so individuals don’t have to navigate their neuromuscular disease journey alone. As a member of the MDA Community, one of the many ways you can connect with others and share your personal story is by joining an MDA Community Group. Community Groups are supportive groups that provide a safe place to gather resources, interact meaningfully with others, and exchange valuable information with others in the neuromuscular disease community.

Provides a voluntary health agency working to defeat muscular dystrophy and related diseases through programs of worldwide research, comprehensive services, and far-reaching professional and public health education. Offers the opportunity to attend week-long camp, in-person or virtual, for ages 8 years through 17 years. Helps with one-on-one support to navigate programs, services, activities, and more. Operates local offices virtually.