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Resources for Families with HD | Genetic Discrimination | HD Citations, Library Resources | Nat'l & Internat'l HD Orgs
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National & International HD Organizations


Huntington's Disease Society of America - a national non-profit voluntary health agency dedicated to finding a cure for Huntington's Disease. The site has an abundance of resources for families seeking movement disorder clinics, long-term care facilities, genetic counselors, social workers, self-help and support groups listed by state.

Huntington Society of Canada - a national network of volunteers and professionals united in the fight against HD since 1973. Their goal is to find new treatments and ultimately a cure for Huntington disease, and to improve the quality of life for people with HD and their families. Their website offers information in both English and French.

International Huntington Association (IHA) - a federation of national voluntary health agencies that share common concern for individuals with Huntington's Disease (HD) and their families. Each agency promotes lay and professional education; individual and family support; psycho-social, clinical and biomedical research; and ethical and legal considerations related to Huntington's Disease in its respective country. A list by country of available services can be found through the "Addresses" link on this site.



Australian Huntington Disease Association, (Inc.)
    New South Wales
    Queensland
    Western Australia

Austrian Huntington Association 

Enfermedad de Huntington - for information in Spanish.

Georgia Chapter of HDSA  

German Huntington Help - you can also navigate this site in either French or English by clicking on one of the flags on the home page.

HDA Online - the Web site of the UK's Huntington's Disease Association, which offers news and information about Huntington's Disease for people affected, their families & friends and health care professionals.

Huntington's Disease Society of America - a national non-profit voluntary health agency dedicated to finding a cure for Huntington*s Disease. The site has an abundance of resources for families seeking movement disorder clinics, long-term care facilities, genetic counselors, social workers, self-help and support groups listed by state.

Huntington Society of Canada - a national network of volunteers and professionals united in the fight against HD since 1973. Their goal is to find new treatments and ultimately a cure for Huntington disease, and to improve the quality of life for people with HD and their families. Their website offers information in both English and French.

International Huntington Association (IHA) - a federation of national voluntary health agencies that share common concern for individuals with Huntington's Disease (HD) and their families. Each agency promotes lay and professional education; individual and family support; psycho-social, clinical and biomedical research; and ethical and legal considerations related to Huntington's Disease in its respective country. A list by country of available services can be found through the "Addresses" link on this site.

Los Angeles chapter of the Huntington's Disease Society of America 

Society for Neuroscience  - dedicated to educating and informing its members and the general public about the results and implications of research relating to the nervous system.

 

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