In 1993, 25 years after her family launched their foundation, the group of scientists they supported finally identified the ...

"I want more time, more memories, and the chance for a better life than my father’s," writes Rachel Reising, who has ...

For decades, families like mine affected by Huntington’s disease have faced a relentless neurological illness with no treatment to slow or stop its progression. Today, that may be changing— but ...

The rare illness affects an individual's ability to move and think, as well as their mental health Lexi Lane is a weekend banking writer at PEOPLE. She first joined as a member of the PEOPLE App team ...

Amy Aungst, center right, organizes walks in Cape Henlopen, Delaware, to raise awareness about Huntington’s disease, a rare condition that is estimated to affect about 30,000 or more U.S. adults.

Mayor Dwain L. Hahs has officially proclaimed May 2026 as Huntington’s Disease Awareness Month in the City of Jackson, ...

Summer is just around the corner, and that means plenty of events and fundraisers will be making their way to Sioux City; one ...

A gene therapy called AMT-130 appears to be the first treatment to slow the progression of Huntington’s disease, an inherited and fatal neurological disorder that has resisted every previous attempt ...

Providing help and hope is the main mission for Huntington's Disease Society of America. And they truly deliver on both. Not only are they advocates who push for research, they also give a helping ...