HDSA has support groups for everyone affected by Huntington’s disease!. To learn more about a support group near you, visit: #LetsTalkAboutHD #HuntingtonsDisease #HDFamily #FamilyIsEverything

¿Sabías que HDSA también alberga grupos de apoyo en español?. Utilice el enlace a continuación para obtener más información:. #HablemosDeHD

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With the crisp air and leaves changing color, it is evident that Fall 🍂 is on the horizon, but HDSA events are just starting to heat up!. To learn more and register, visit: #LetsTalkAboutHD #HuntingtonsDisease #HDSA

Happy Labor Day From HDSA!. At HDSA, we believe that #FamilyIsEverything, and no one faces #HuntingtonsDisease alone. To learn more visit #Laborday #HuntingtonsDisease #LetsTalkAboutHD.

Every monthly donation to HDSA helps make a real difference — supporting social workers, care at HDSA Centers of Excellence, and advancing vital HD research. To learn more, visit: #HDSA #HuntingtonsDisease #LetsTalkAboutHD

📝 Are you ready to register for a 2025 HDSA Team Hope Walk?. Follow these simple steps and help make a meaningful impact for HD families!. 🔗 Register today at #hdsa #familyiseverything #LetsTalkAboutHD

Do you an old vehicle collecting dust?. Put it to good use—donate it to the Huntington's Disease Society of America and help support families affected by Huntington’s disease. Learn more at: #HuntingtonsDisease #LetsTalkAboutHD #VehicleDonation

#letstalkabouthd with Chelsea Roberts, and the Pacific West Region. Check out this news segment from KATU TV highlighting the 2025 HDSA Team Hope Walk: Learn more about the Portland Team Hope Walk, click here: #HDSAFamily

#FamilyIsEverything.Make sure yours is cared for, no matter what. HDSA has partnered with FreeWill to offer a free, secure way to write your will online. In just 20 minutes, from the comfort of your home. For more information, visit: #LetsTalkAboutHD

HDSA offers an array of support group options for individuals and families affected by Huntington’s disease at any stage. To learn more, visit: #LetsTalkAboutHD #HuntingtonsDisease #HDFamily

Join us on Sept. 18th, 2025 for a very special 24 hour day of giving dedicated to Marjorie Guthrie. On Founder's Day, we honor Marjorie and her legacy by raising critical funds, voices, and awareness for the HD community. Learn more and add to calendars:.

Summer might be winding down, but the HDSA events are just starting to heat up! Turn the page to September with purpose, team up with HDSA to support those affected by Huntington’s disease. Learn more: #LetsTalkAboutHD #HuntingtonsDisease #HDSA

¿Sabías que HDSA también alberga grupos de apoyo en español?. Utilice el enlace a continuación para obtener más información:. #HablemosDeHD

HDSA provides a range of support group options for individuals and families affected by Huntington’s disease at any stage. To learn more visit: #HuntingtonsDisease #HDFamily #FamilyIsEverything

New Disability Tips vlog: "Make-A-Will Month 2025," hosted by Allison Bartlett, Esq., Senior Manager of Disability Programs. To read the blog post, click: And learn more about FreeWill, here: #DisabilityTips #LetsTalkAboutHD

Join us for a powerful evening of celebration, recognition, and inspiration at the 40th Annual Huntington’s Disease Society of America (HDSA) Convention Gala & National Awards. Link: #HDSAConvention #HuntingtonsDisease #FamilyIsEverything

If you have an upcoming birthday or significant anniversary to celebrate this year, and you're interested in celebrating by raising awareness and support for those living with HD. Make the most of your day by setting up a fundraiser on Facebook or Instagram with HDSA. #HDSA

HDSA has partnered with FreeWill to offer a free, secure way to write your will online, from the comfort of your home. #FamilyIsEverything.Make sure yours is cared for, no matter what. 👉 Learn more by clicking here:

The newest video from the 40th Annual Huntington’s Disease Society of America Convention, held in Indianapolis, Indiana, "Clinical Trials Showcase," is now available on our YouTube page. Link: #HDSA #HuntingtonsDisease #ClinicalTrials

Summer’s not over yet! . This August, join HDSA as we walk, run, cheer and golf to raise awareness, and support to those affected by Huntington’s disease. To learn more and register, visit: #LetsTalkAboutHD #HuntingtonsDisease #HDSA