Connect with our local chapter:
  • HELP HOPE BLOSSOM

    The amaryllis flower is a symbol of strength and hope for the Huntington’s disease community. Every holiday season, HDSA sells beautiful varieties that also make for great gifts for friends and family. ORDER TODAY WHILE SUPPLIES LAST!

  • #LetsTalkAboutHD with Debra Andrew

  • #LetsTalkAboutHD with Morgan Pratt

  • #LETSTALKABOUTHD WITH JENNIFER BANDLEY

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

  • VIRTUAL 35TH ANNUAL HDSA CONVENTION

    Thank you for attending & supporting the Virtual 35th Annual HDSA Convention. All recorded sessions are now available!

  • 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.

  • HDSA & ME: EDUCATE. ENGAGE. EMPOWER.

    HDSA is pleased to announce a new virtual educational series for the Huntington’s disease community.

  • 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.

  • 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.

  • 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.

  • FOLLOW US ON INSTAGRAM

    Staying connected with the HDSA on Instagram is a fantastic way for you stay up-to-date with the latest information about Huntington's Disease in Utah. #hdsafamily #hdsaut #hdstrong #curehd #hdsa #hd

  • FOLLOW US ON FACEBOOK

    Staying connected with the HDSA on Facebook is the best way for you stay up-to-date with the latest information about Huntington's Disease in Utah. #hdsafamily #hdsaut #hdstrong #curehd #hdsa #hd

  • 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.

  • PARTICIPATE IN A VIRTUAL HDSA TEAM HOPE WALK

    The battle against Huntington’s disease rages on and we need you to join TEAM HOPE – VIRTUALLY! A virtual walk is a real walk, but on your terms. You get choose your own course. Now, you can take part wherever you are…from the comfort and safety of your own home, around your yard, or even your neighborhood (following social distance guidelines, of course).

  • DONATE TO THE UTAH CHAPTER

    All proceeds will help those affected by Huntington's Disease in Utah. Your donations will help with support groups, treatments, education, research, and so much more.