HDSA’s 35th Annual Convention Goes Virtual!
In light of COVID-19, we have decided it is in the best interest of our families to convert to a virtual event. The Virtual Convention will continue to take place in June, but the exact timing of events is likely to change to accommodate a nationwide online audience.
HDSA 2019 YEAR IN REVIEW MAGAZINE
Take a look back on the highlights from this past year & join us as we keep the momentum moving forward into 2020.
THE MARKER: HDSA’S 2019 RESEARCH REPORT
A look back on clinical trials, conferences, fellowships and promising developments in HD research.
THIS WEEK IN HD RESEARCH
Dr. Leora Fox keeps you up-to-date on HDSA research activities, recently published work about Huntington’s disease, historical moments in HD research and more.
SHARE YOUR JOURNEY
Help us turn up the global volume on HD awareness & #LetsTalkAboutHD. Join the conversation on social media & share your story today!
HDSA CENTERS OF EXCELLENCE
The HDSA Centers of Excellence provide an elite multidisciplinary approach to Huntington’s disease care and research. HDSA currently has 50 Centers of Excellence across the U.S.
FREE TELEHEALTH COUNSELING
Announcing free online therapy sessions for people affected by HD provided by HDSA & American Well®. HDSA-trained licensed social workers and psychologists will be available to HD families in all 50 states.
PARTICIPATE IN A CLINICAL TRIAL
HD Trialfinder identifies trials nationwide looking for participants that share the same diagnosis, stage and treatment history.
PARTICIPATE IN AN HDSA TEAM HOPE WALK
The Team Hope Walk program is our signature grassroots fundraising campaign designed to provide hope and support for those touched by this devastating disease. HDSA Team Hope Walks are sponsored nationally by Genentech and Teva Pharmaceuticals. Find an event in your area!