HDSA Telehealth- a free internet-based program powered by Amwell, that brings qualified HD knowledgeable licensed social workers and psychologists to the HD community.
Each year, HDSA holds a National Convention that includes sessions that inform the HD Community about research, support, and more. For more information, click here
Motivates youth to get involved in their local HDSA Chapters, Affiliates, and Support Groups in efforts through education, fundraising, advocacy and awareness for Huntington’s disease. The NYA is a collection of children, teens and young adults from across the country. To learn more about the NYA, click here
The conversation series tackles important topics to help you navigate through your HD journey. Episodes air on HDSA’s YouTube channel and will include discussions about isolation, testing, relationships, family planning & much more. Hosted by Jennifer Simpson, the series allows members of the HD community to submit questions & some will be featured in the upcoming segment. To watch more episodes, click here
Connecting young adults impacted by a rare or chronic condition with social and emotional support in the hope of improving their quality of life. Online support for your adults with rare disease, founded by someone who is gene positive. For more information, click here
