HDSA-Tennessee Chapter

HDSA-Tennessee Chapter We are a part of HDSA's South Region. We strive to provide support and information to Tennessee families.

HDSA is the premier nonprofit organization dedicated to improving the lives of everyone affected by Huntington’s disease and their families.

🚨 Just announced & on sale now 🚨Join us on Sunday afternoon on May 31st for I Get By With A Little Help From My Friends ...
05/21/2026

🚨 Just announced & on sale now 🚨
Join us on Sunday afternoon on May 31st for I Get By With A Little Help From My Friends - A Day of Music and Community Together in the Fight Against HUNTINGTONS DISEASE featuring Jake Burman and Company, Henry Cruz Band with special performances by: Wendy Moten + Judy Paster!

Get your tickets here ->

Find tickets for I Get By With A Little Help From My Friends - A Day of Music and Community Together in the Fight Against HUNTINGTONS DISEASE, Jake Burman and Company, Henry Cruz Band, Wendy Moten, Judy Paster showing at the 3rd and Lindsley - Nashville, US Sunday May 31, 11:00AM Tickets starting at...

We would love to see everyone at this amazing Huntington’s Disease Society of America Tennessee Chapter event! Your supp...
05/21/2026

We would love to see everyone at this amazing Huntington’s Disease Society of America Tennessee Chapter event! Your support, advocacy, and presence mean so much to families affected by Huntington’s Disease. We hope to see you there as we continue raising awareness and building a stronger community together! 💙

🚨 Just announced & on sale now 🚨
Join us on Sunday afternoon on May 31st for I Get By With A Little Help From My Friends - A Day of Music and Community Together in the Fight Against HUNTINGTONS DISEASE featuring Jake Burman and Company, Henry Cruz Band with special performances by: Wendy Moten + Judy Paster!

Get your tickets here -> https://bit.ly/489nNq9

05/02/2026

Cure HD

02/28/2026

Today, on Rare Disease Day, we stand for families fighting battles most may never see and whose voices are too often unheard.💙💜

So take a moment:
A like can spread awareness.
A share amplifies a voice.
A donation can fuel hope.

Small actions creating life-changing impact. And today, if you can, your donation will be matched dollar for dollar. It will have twice the impact.
DONATE NOW:https://give.hdsa.org/campaign/766544/donate

💙💜🦋Meet Our 2026 HDSA Tennessee Youth Ambassador, Demi! 💙💜🦋Demi has been part of the HDSA Tennessee family for over a de...
01/21/2026

💙💜🦋Meet Our 2026 HDSA Tennessee Youth Ambassador, Demi! 💙💜🦋

Demi has been part of the HDSA Tennessee family for over a decade, and we couldn’t be more proud to see her step into this leadership role. As Youth Ambassador, she will work to raise awareness, educate others, promote our chapter, and help secure sponsors to support families impacted by Huntington’s disease.

Neurocrine Biosciences and Teva Pharmaceutical Industries Ltd. have been incredible as the 2025 National Sponsors for ea...
12/17/2025

Neurocrine Biosciences and Teva Pharmaceutical Industries Ltd. have been incredible as the 2025 National Sponsors for each Team Hope Walk event across the country! Thank you so much for helping families facing Huntington’s disease alongside us!

We love having uniQure’s gift of support and partnership as our Regional Sponsor for our Team Hope Walk events across th...
12/15/2025

We love having uniQure’s gift of support and partnership as our Regional Sponsor for our Team Hope Walk events across the region! Thank you uniQure!

Thank you Neurocrine Biosciences and Teva Pharmaceutical Industries Ltd. for supporting us in the fight against Huntingt...
12/03/2025

Thank you Neurocrine Biosciences and Teva Pharmaceutical Industries Ltd. for supporting us in the fight against Huntington’s disease all of 2025 as the National Sponsors for Team Hope Walk events across the United States!

Thank you uniQure! Your support as Regional Sponsor for Team Hope Walk events across our region is such a special gift f...
12/01/2025

Thank you uniQure! Your support as Regional Sponsor for Team Hope Walk events across our region is such a special gift for families facing Huntington’s disease.

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New York, NY

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