Huntington's Disease Society of America
- Our Mission
- HDSA Goals - Mission in Action
- Find your local HDSA Chapter, Affiliate or Regional Office
- Staff directory
- Financials
- Board of Trustees
- Careers
-
Faces of HD
- Meet Sue
- Meet Sandra
- Meet Hope
- Meet Erika & Melissa
- Meet Daniel
- Meet The Timberlake/Begley family
- Meet Evelyn
- Meet Rosalie
- Meet Jim
- Meet Jennifer
- Meet Katie
- Meet Mackenzie & Jesse
- Meet The Decker's
- Meet Carl
- Meet Shana & Debbie
- Meet Kirsten
- Meet Dylan
- Meet Deb
- Meet Chrissy
- Meet Lacy
- Meet KayCee
- Meet Michelle
- Meet Stevie
- Meet Lindsay & Thomas
- Meet Dave & Susie
- Meet Lauren
- Past Faces of HD
- Meet Eva
- Meet Mimi
- Meet Jessica
- Meet Kristen
- Meet Marcy & Jim
- Meet Bike for the Cure
- News & Announcements Archive
- HD and HDSA In The News
- Thank You Thursday
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Huntingtons disease (HD) affects one in every 10,000 Americans, and another 200,000 people are at risk of inheriting it from an affected parent. With no effective treatment or cure, Congress cannot ignore this disease. I am proud to sponsor of the HD Parity Act which waives the 24-month waiting period for coverage under the Medicare program for individuals diagnosed with Huntington's disease.
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