Serves as a place for persons with Becker Muscular Dystrophy to exchange information and communicate with others about the disease.

Not-for-profit medical research foundation working to find a treatment for muscular dystrophy and other genetic diseases through cell/gene therapy. Site describes treatments and clinical trials.

Lifestyle options, conventional medical interventions and information for people interested in Duchenne muscular dystrophy.

This site highlights the work of Dr. John R. Bach and provides information about Non-Invasive Ventilation (NIV) and pulmonary care.

The FSH Society address issues and needs related to FacioScapuloHumeral Muscular Dystrophy (FSHD).

Personal web page of a Russian woman living with Spinal Muscular Atrophy. Includes information on travel, recipes and psychology. English, Russian and Italian versions.

A site by, for, and about Justin Sokolowski, a young man with Werdnig Hoffman's disease or a form of SMA. Lots of pictures of friends and family (including his cats), plus pictures of Justin with many pro and semi-pro athletes he's met. Guestbook. Virginia.

Kevin, who has Duchenne Muscular Dystrophy, attends the University of Louisville and has a web business as well. Interests, hobbies and accomplishments plus lots of MD links. Kentucky.

Reference for parents of boys with Duchenne Muscular Dystrophy. Along with practical and health-related articles are poetry and personal stories.

Dedicated to educating potential parents about Myotonic Dystrophy and genetic testing. Information about fundraising, both for research and to assist people who cannot afford testing, news, stories, and about Logan Paige.

Mark Reich has DMD and is a resident of Massachussets. He is vice-chair of his local conservation commission and is an avid gardener.

Pennsylvania ride to benefit the Muscular Dystrophy Association. Information on results, money raised and its distribution. Sponsored by the Eastern Harley-Davidson Dealers Association, held annually in May.

Extensive information on the range of disorders, research information and many links to onsite publications. Also provides an international support network with a chat service dedicated for use by the worldwide Muscular Dystrophy community.

The Muscular Dystrophy Association of South Australia provides a range of individually designed support services for all persons with muscular dystrophy and neuromuscular disorders, their families and their carer/support provider, including therapy, information, equipment loan and counselling.

Voluntary health agency providing information and supporting research into neuromuscular diseases, including Muscular Dystrophy. The MDA site contains information about many forms of muscular dystrophy, including lists of ongoing clinical trials, an 'Ask the Experts' feature, and research updates.

Organization dedicated to serving people with muscular dystrophy and other neuromuscular diseases who live in New Zealand.

Muscular Dystrophy Association of Slovenia

Muscular Dystrophy Association Singapore (MDAS) is a self-help organization committed to uplift the lives of people with Muscular Dystrophy.

Northern Ireland branch of Muscular Dystrophy Campaign includes news, events, staff profiles, information about the Regional Muscle Clinic and a web directory.

National voluntary agency committed to eliminating neuromuscular disorders.