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Huntington's Disease was first recognized as an inherited disorder in 1872 when a 22-year-old American doctor, George Huntington, wrote a paper called On Chorea. His paper was later published in the Reporter of Philadelphia and the disorder he described became known as Huntington's Chorea.

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People with HD usually die within 10 to 30 years following symptom onset, most commonly from infections, most often pneumonia and injuries related to falls. Huntington's disease causes disability that gets worse over time. Currently no treatment is available to slow, stop, or reverse the course of HD

Huntington's disease is a condition that stops parts of the brain working properly over time. It's passed on or inherited from a person's parents. It gets gradually worse over time and is usually fatal after a period of up to 20 years.