-
HD SYMPTOMS AND TREATMENT IMPACT SURVEY
This first-of-its kind survey has been created by the HD community for the HD community. When you take this survey, you will be informing the FDA, NIH and medical product developers how you describe the challenges of living with HD, manage symptoms, and define the value of new treatments.
-
TAKE ACTION NOW!
You can participate in the HDSA Externally-led Patient Focused Drug Development (EL-PFDD) Meeting for Pre-symptomatic and Early to Mid-Stage Adult Onset of HD, on November 13, 2024.
-
JOIN POWER HD
By generating the most comprehensive patient-driven Huntington’s disease data we can accelerate research and the development of new drugs, devices, or other therapies. YOU HAVE THE POWER.
-
FOUNDER'S DAY
Please join us on September 18th, 2024, for a very special 24-hour day of giving dedicated to Marjorie Guthrie. On Founder's Day, we honor Marjorie and her legacy by raising critical funds, voices, and awareness for the HD community all over the country, and across the world.
-
SAVE THE DATE!
Join us for the 40th Annual HDSA Convention in Indianapolis, Indiana on June 26-28, 2025 This is your unique chance to connect, learn, inspire and get inspired. Our convention is not just an event – it’s a celebration, it’s magic!
-
HDSA Publishes 2023 Year In Review Magazine
Take a look back on HDSA's achievements and top stories from 2023 in the latest Year In Review Magazine.
-
Annual HDSA Convention Registration is Now Open!
Join us for the 39th Annual HDSA Convention in Spokane, Washington, May 30- June 1, 2024
-
THE MARKER: 2023 HDSA RESEARCH REPORT
In 2023, HDSA supported fantastic Huntington’s disease science, shared research news with the community, and amplified family voices in drug development. The latest issue of The Marker is now available!
-
2024 STRIKE OUT HD
SATURDAY, MARCH 11TH @ 4PM
WOODLAND BOWL
3421 EAST 96TH STREET
INDIANAPOLIS, INDIANA -
FIND HDSA RESOURCES NEAR YOU
HDSA provides world-class support programs and resources across the country for everyone impacted by Huntington’s disease. Visit our interactive map to get started today!
-
HDSA SOCIAL WORKERS
HDSA Social Workers are often the first voice that someone new to HD may hear. Social workers offer information, education and access to community based services within a specific region.
-
HDSA SUPPORT GROUPS
HDSA support groups are free for individuals, their loved ones, and families impacted by Huntington’s disease.