• Join HDSA on Rare Disease Day – February 28th!

    On February 28th, lets show our strength—together. This year, we’re counting on you to help us raise $15,000 and unlock our matching gift challenge, doubling our impact to $30,000 in support of HDSA programs, research, and family services. We can’t do this without you! DONATE TODAY!

  • MEET OUR NEW PRESIDENT AND CEO AMY GRAY

    We are excited to announce that Amy Gray has joined our organization as the new President and Chief Executive Officer.

  • Watch the HDSA EL-PFDD Meeting!

  • 2023 HDSA Annual Report

    We’re thrilled to announce the release of the 2023 HDSA Annual Report, highlighting the amazing progress we've achieved as One HDSA.

  • 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.

  • Registration is Now Open!

    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.

  • 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.

  • South Carolina Wins Affiliate of the Year

    The collaborative spirit of the South Carolina Affiliate Leaders led to a successful year in outreach, fundraising, and growth. Congratulations, South Carolina!