Sites 13
Promotes awareness, raises funds, and offers an online community for patients and parents. Based in the United Kingdom.
Founded by parents of a patient, to raise funds for research. California.
FED is a non-profit organization established to find a cure for Duchenne Muscular Dystrophy, the leading lethal childhood genetic disease.
The FSH Society address issues and needs related to FacioScapuloHumeral Muscular Dystrophy (FSHD).
Includes 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.
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.
National voluntary agency committed to eliminating neuromuscular disorders.
Nonprofit foundation that provides adaptive equipment and emotional support to individuals and families affected by any one of 40 neuromuscular diseases.
Voluntary organization in Ireland which provides support for people with muscular dystrophy and their families.
Parent Project Muscular Dystrophy is a not-for-profit organization founded in 1994 by parents of children with Duchenne and Becker Muscular Dystrophy.
The FSH Society address issues and needs related to FacioScapuloHumeral Muscular Dystrophy (FSHD).
Promotes awareness, raises funds, and offers an online community for patients and parents. Based in the United Kingdom.
Founded by parents of a patient, to raise funds for research. California.
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.
Includes 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.
National voluntary agency committed to eliminating neuromuscular disorders.
Muscular Dystrophy Association Singapore (MDAS) is a self-help organization committed to uplift the lives of people with Muscular Dystrophy.
Muscular Dystrophy Association of Slovenia
Voluntary organization in Ireland which provides support for people with muscular dystrophy and their families.
Nonprofit foundation that provides adaptive equipment and emotional support to individuals and families affected by any one of 40 neuromuscular diseases.
Organization dedicated to serving people with muscular dystrophy and other neuromuscular diseases who live in New Zealand.
Parent Project Muscular Dystrophy is a not-for-profit organization founded in 1994 by parents of children with Duchenne and Becker Muscular Dystrophy.
FED is a non-profit organization established to find a cure for Duchenne Muscular Dystrophy, the leading lethal childhood genetic disease.
Last update:
April 11, 2020 at 21:12:50 UTC
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Society: Ethnicity: Slavic: Ukrainian: Ukrainian-Canadian
- Recently edited by shedragon
- Recently edited by shedragon