HD Awareness Month 2:1 Match

This HD Awareness Month, your gift can go even further. Thanks to a generous 2:1 match, every dollar donated will have double the impact for HD families across the country. Help turn awareness into action and hope into progress.

THIS MAY

Help us turn up the global volume on HD Awareness by sharing your stories, photos & videos to social media using #LetsTalkAboutHD

Explore the Voice of the Patient Report to hear directly from people and families living with Huntington’s disease — their stories, struggles, and hopes that will help shape the future of care and advocacy.

📣 Share your voice! Take the HDSA Strategic Plan Survey and help shape the future of our mission.

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!

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.