What is Huntington's Disease?

HD is a familial disease, passed from parent to child through a mutation on the 4th chromosone. Each child of an HD parent has a 50-50 chance of inheriting the gene which causes degeneration of brain cells, resulting in the loss of ability to walk, think, talk, reason, and swallow. Onset generally appears at midlife, but in some onset occurs in childhood (juvenile HD) or in old age (late onset). The disease profoundly affects the lives of entire families, as an affected person becomes totally dependent on others for his/her care. About one in 10,000 Americans have this disease. Since 1993, a genetic test has been available to those at-risk, to determine whether or not they carry the HD gene. The test does not indicate at what age the disease will develop. Your contribution will expedite this great scientific endevor and help fund family services for those afflicted with this uniquely devastating neurological disease.

For more information:

HDSA 1-800-345-HDSA
Huntington's Society of Canada
HD Advocacy Center
Huntington's Study Group

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