Connect with our local chapter:
  • #LetsTalkAboutHD with Debra Andrew

  • #LETSTALKABOUTHD WITH JENNIFER BANDLEY

    Jennifer Bndley is raising awareness about Huntington's Disease by running a marathon.

  • THE MARKER: HDSA’S 2020 RESEARCH REPORT

    Updates on clinical trials, fellowships, conferences and the latest in HD research.

  • COVID-19 & HD RESOURCES

    We know the COVID-19 pandemic is a difficult time for all and may be particularly challenging for those living with or supporting someone with Huntington’s disease. HDSA is committed to sharing the latest updates and resources as we face this public health crisis together.

  • 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.

  • HUNTINGTON'S DISEASE UTAH SUPPORT GROUP

    Are you affected by Huntington's Disease? Are you at-risk? Does it run in your family? How do you know when it's time to get tested? Should you put your loved one in a home? Or are you trying to learn more about the disease to help a friend? We can help you find the resources that you need. Join us. Bring your family and friends. We are stronger together.

  • FAMILY PLANNING

    Are you planning your family? Have you considered IVF--or in vitro fertilization? One organization--End HD--wants to pay for a couple's in vitro fertilization process in an attempt to stop the spread of the HD gene. Apply to see if you qualify to have your IVF paid for.

  • PASS THE HD PARITY ACT

    We need your support to pass the HD Parity Act which will waive Medicare’s two-year waiting period for people with Huntington’s disease. It is time to take action because two years is too long!