HDSA Centers of Excellence Program Expands to 68 Sites

The Huntington’s Disease Society of America (HDSA) is expanding its HDSA Centers of Excellence network of comprehensive care clinics with 57 grants totaling $2,100,285. In addition to the 57 grant funded facilities, eleven regional partner sites were also named, ensuring expert HD care at 68 distinct medical facilities in 37 states across the nation and Washington, DC.

SCHOLARSHIP APPLICATIONS NOW OPEN!

HDSA offers multiple scholarships to help you and your family attend the 39th Annual HDSA Convention. Whether you are a first-time HDSA Convention attendee, a member of HDSA’s National Youth Alliance, or a resident of Washington, Kentucky or New Jersey, we will help you get to Spokane!
SCHOLARSHIP APPLICATION DEADLINE: FRIDAY, MARCH 1st

Annual HDSA Convention Registration is Now Open!

Join us for the 39th Annual HDSA Convention in Spokane, Washington, May 30- June 1, 2024
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!
So, why the wait? Register today and secure your seat!

  

The Marker: 2023 HDSA Research Report

The Marker highlights HDSA’s efforts in research supported directly by the organization to keeping the larger community informed about what is happening in HD science. The latest issue of The Marker is now available!

Let’s protect the ones we love this National Estate Planning Awareness Week with HDSA’s new partnership with FreeWill!

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 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.

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