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Organizations

Sites:

» Cell Therapy Research Foundation Open in a new browser window - 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.
» Facioscapulohumeral Muscular Dystrophy Society Open in a new browser window - The FSH Society address issues and needs related to FacioScapuloHumeral Muscular Dystrophy (FSHD).
» Foundation to Eradicate Duchenne, Inc. Open in a new browser window - FED is a non-profit organization established to find a cure for Duchenne Muscular Dystrophy, the leading lethal childhood genetic disease.
» Logan Paige Foundation for Myotonic Dystrophy Open in a new browser window - 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.
» MDA Europe Foundation Open in a new browser window - European fund raising foundation for Muscular Dystrophy in relation with Harley-Davidson events, H.O.G. Chapter events and Harley-Davidson dealers within the European community.
» Muscular Dystrophy Association (Australia) Open in a new browser window - 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.
» Muscular Dystrophy Association (South Australia) Open in a new browser window - 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, infor
» Muscular Dystrophy Association (USA) Open in a new browser window - 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 &quo
» Muscular Dystrophy Association Singapore Open in a new browser window - Muscular Dystrophy Association Singapore (MDAS) is a self-help organization committed to uplift the lives of people with Muscular Dystrophy.
» Muscular Dystrophy Association of New Zealand Open in a new browser window - Organization dedicated to serving people with muscular dystrophy and other neuromuscular diseases who live in New Zealand.
» Muscular Dystrophy Association of Slovenia Open in a new browser window - Muscular Dystrophy Association of Slovenia
» Muscular Dystrophy Canada Open in a new browser window - National voluntary agency committed to eliminating neuromuscular disorders.
» Muscular Dystrophy Family Foundation Open in a new browser window - Nonprofit foundation that provides adaptive equipment and emotional support to individuals and families affected by any one of 40 neuromuscular diseases.
» Muscular Dystrophy Ireland Open in a new browser window - Voluntary organization in Ireland which provides support for people with muscular dystrophy and their families.
» Parent Project Muscular Dystrophy Open in a new browser window - Parent Project Muscular Dystrophy is a not-for-profit organization founded in 1994 by parents of children with Duchenne and Becker Muscular Dystrophy.
» Parent Project Muscular Dystrophy in Nepal Open in a new browser window - Parent Project Muscular Dystrophy in Nepal focuses on Duchenne and Becker Muscular Dystrophy, by providing practical, medical and emotional support to the people and families affected by the condition.
» Society for Muscular Dystrophy Information International Open in a new browser window - Features organization background, disease information, newsletters, membership information, resources, and contact details.


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