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The Society is a National, voluntary health organization dedicated to improving the lives of people with Huntington's Disease and their families.
To promote and support research and medical efforts to eradicate Huntington's Disease.
To assist people and families affected by Huntington's Disease to cope with the problems presented by the disease.
To educate the public and health professionals about Huntington's disease.
Huntington's Disease is a devastating, hereditary, degenerative brain disorder for which, presently, there is no cure and only one FDA-approved treatment for a sympton of HD. HDSA provides vital support, information and educational services to improve the lives of those affected by HD, offering resources and guidance for HD families.
- Kirsten Waldschmidt
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