July, 2021
HD Advocate Testifies on HD Parity Act
Posted on July 29, 2021
Kala Booth, a Huntington’s disease positive individual and caregiver to her mother, will appear TODAY before the House Committee on Energy & Commerce subcommittee on neurodegenerative diseases. Kala…
Read MoreNow Accepting Letters of Intent for 2022 HDSA Centers of Excellence!
Posted on July 22, 2021
HDSA Centers of Excellence provide comprehensive multidisciplinary clinical services to families affected by HD, including neurology, psychology, genetic counseling/testing, social…
Read MoreNew Biomarkers to Track Disease-Modifying Therapies in Pre-manifest HD
Posted on July 15, 2021
Much of today’s efforts in HD research are focused on lowering huntingtin protein in early stages of the disease. Ideally, clinicians could begin…
Read MoreRecorded Sessions From The HDSA Convention Are Now Available
Posted on July 8, 2021
The Virtual 36th Annual HDSA Convention was a spectacular time for researchers, clinicians, family members, and affected individuals to come together for…
Read MoreOpportunities to participate in online HD research
Posted on July 1, 2021
Research participation is essential in the quest for HD treatments and knowledge, not only in pursuit of drug development but also to improve care…
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