HDSA partners with RARE-X.

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 hold the key to unlock future discoveries.

INTRODUCING THE HDSA PODCAST

The HDSA Podcast, hosted by Louise Vetter, gives listeners an opportunity to meet members of the Huntington’s disease community and get a behind-the-scenes look at the Huntington’s Disease Society of America.

HDSA CENTERS OF EXCELLENCE NETWORK EXPANDS TO 67 SITES

The Huntington’s Disease Society of America is expanding its HDSA Center of Excellence network of comprehensive care clinics with 56 grants totaling more than $2 million. In addition to the 56 grant funded facilities, eleven regional partner sites were also named, ensuring expert HD care at 67 distinct medical facilities in 36 states across the nation and Washington, DC.

HDSA Publishes 2022 Year In Review Magazine

Take a look back on HDSA‘s achievements and top stories from 2022 in the latest Year In Review Magazine. 

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.

PARTICIPATE IN AN HDSA EVENT NEAR YOU

From Team Hope Walks and Celebrations of Hope Galas to Education Days and Webinars, HDSA has events across the country for you and your family to get involved in the fight against Huntington’s disease.