HDSA Indiana Chapter

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

Huntington’s Disease: A Comprehensive Family Caregiver’s Guide by George C Dow• George has over 20 years experience with...
01/02/2026

Huntington’s Disease: A Comprehensive Family Caregiver’s Guide by George C Dow

• George has over 20 years experience with caregiving for loved ones with HD. He’s used this knowledge and experience to create a guide book specifically for HD.
• Ranked the # 8 bestselling eBook in the United States today for Genetic Disorders & Diseases.
• Starting today through January 5, 2026, Amazon is offering this Kindle eBook absolutely FREE.
• Link in our bio to order or order here: https://a.co/d/gB4EZlO



We need your voice!Take Action Now, Stand Up for AMT-130AMT-130, a promising gene therapy for Huntington’s disease, is a...
12/27/2025

We need your voice!

Take Action Now, Stand Up for AMT-130

AMT-130, a promising gene therapy for Huntington’s disease, is at risk of not getting a full, fair FDA review. After decades without a treatment that slows or stops HD, families cannot afford delays.

Ask your Members of Congress to urge the FDA to allow AMT-130 to move forward to a science-driven review.

Your message right now can help keep hope moving forward.

🔗 hdsa.org/advocacyhome/TakeAction

HDSA is planning the path ahead for the next three years, and your input can help lead the way.If Huntington’s disease t...
12/26/2025

HDSA is planning the path ahead for the next three years, and your input can help lead the way.

If Huntington’s disease touches your life, we’d love to hear your perspective.

Take the quick survey at: https://fs22.formsite.com/hdsa/olqg4bsvru/index to help guide HDSA’s work through the year 2028.

12/23/2025

Take Action Now — Stand Up for AMT-130

AMT-130, a promising gene therapy for Huntington’s disease, is at risk of not getting a full, fair FDA review. After decades without a treatment that slows or stops HD, families cannot afford delays.

We need your voice!

Ask your Members of Congress to urge the FDA to allow AMT-130 to move forward to a science-driven review.

For people living with HD, every day matters.

Your message right now can help keep hope moving forward.

🔗 hdsa.org/advocacyhome/TakeAction

We’re Going LIVE with HDBuzz, tomorrow, December 17th at 12:00 PM EST! 🎥🔬HD research can be complicated — but getting an...
12/16/2025

We’re Going LIVE with HDBuzz, tomorrow, December 17th at 12:00 PM EST! 🎥🔬

HD research can be complicated — but getting answers shouldn’t be. Join an open Ask the Scientist Anything session where the HDBuzz team breaks down clinical trials, new therapies, and the latest science in real time.

Your questions. Their expertise. No jargon, just clarity. https://hdsa-org.zoom.us/webinar/register/2017652939043/WN_EI8MvkN6RYCUBiB-CrwluQ

🚨 The moment we’ve all been waiting for is finally here! 🚨HDSA is thrilled to announce GoFundMe Pro—our brand-new peer-t...
12/16/2025

🚨 The moment we’ve all been waiting for is finally here! 🚨

HDSA is thrilled to announce GoFundMe Pro—our brand-new peer-to-peer fundraising platform! 🎉

Get ready for a whole new world of fundraising fun. With this new platform, you’ll have even more opportunities to earn Team Hope shirts, early-bird gifts, special incentives, exclusive awards, and so much more!

And the biggest news of all…
✅ Starting in 2026, ALL Team Hope Walks* will be FREE to register! 🎉

👀 Keep a lookout—more exciting updates and information will be shared in January.
*Except endurance events.

Take Action Now — Stand Up for AMT-130AMT-130, a promising gene therapy for Huntington’s disease, is at risk of not gett...
12/16/2025

Take Action Now — Stand Up for AMT-130

AMT-130, a promising gene therapy for Huntington’s disease, is at risk of not getting a full, fair FDA review. After decades without a treatment that slows or stops HD, families cannot afford delays.

We need your voice!

Ask your Members of Congress to urge the FDA to allow AMT-130 to move forward to a science-driven review.

For people living with HD, every day matters.

Your message right now can help keep hope moving forward.

🔗 hdsa.org/advocacyhome/TakeAction

12/15/2025

The deadline to reserve your order is TODAY, Monday, December 15th!

Place your Amaryllis order today!

With over 20 amazing products to choose from, with vibrant amaryllis varieties and fragrant paperwhites! 🌼 Shop with confidence knowing that FP (FlowerPower) guarantees all products will grow beautifully. 🌺

Remember to credit your order to your chapter or affiliate at checkout!

Give a gift that blooms this season! Click: http://HDSA.fpfundraising.com to learn more.

12/14/2025

The deadline to reserve your order is tomorrow, Monday, December 15th!

Place your Amaryllis order today!

With over 20 amazing products to choose from, with vibrant amaryllis varieties and fragrant paperwhites! 🌼 Shop with confidence knowing that FP (FlowerPower) guarantees all products will grow beautifully. 🌺

Remember to credit your order to your chapter or affiliate at checkout!

Give a gift that blooms this season! Click: http://HDSA.fpfundraising.com to learn more.

12/12/2025

Take Action Now — Stand Up for AMT-130

AMT-130, a promising gene therapy for Huntington’s disease, is at risk of not getting a full, fair FDA review. After decades without a treatment that slows or stops HD, families cannot afford delays.

We need your voice!

Ask your Members of Congress to urge the FDA to allow AMT-130 to move forward to a science-driven review.

For people living with HD, every day matters.

Your message right now can help keep hope moving forward. 💙💜

🔗 hdsa.org/advocacyhome/TakeAction

Address

P. O. Box 40464
Indianapolis, IN
46240

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