HDSA Western PA Chapter

HDSA Western PA Chapter HDSA Western PA Chapter provides services locally to families affected with Huntington's disease. The chapter serves families in the Western PA area.

HDSA is the premier nonprofit organization dedicated to improving the lives of everyone affected by Huntington’s disease and their families. Family and Friends meetings are held in Oakland, Pittsburgh on the first Thursday of every month.

Our community powers everything we do—and this is a fun one. 💙Help us choose the next Team Hope Walk T-shirt!🗓️ Online v...
01/12/2026

Our community powers everything we do—and this is a fun one. 💙

Help us choose the next Team Hope Walk T-shirt!

🗓️ Online voting: 1/9–1/23

Visit: https://fs22.formsite.com/hdsa/zs5gdyk81j/index to cast your vote.

🗳️ Help choose the next Team Hope Walk T-shirt!Vote for your favorite design #1– #4 now through 1/9–1/23.✅ Vote here: h...
01/10/2026

🗳️ Help choose the next Team Hope Walk T-shirt!

Vote for your favorite design #1– #4 now through 1/9–1/23.

✅ Vote here: https://fs22.formsite.com/hdsa/zs5gdyk81j/index (only votes through the voting link count!)

Which one are you picking? 👇💙

Remember, our helpline is always available. Call 412.833.8180.
01/01/2026

Remember, our helpline is always available. Call 412.833.8180.

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.

Address

PO Box 1196, 1140 Thorn Run Road
Coraopolis, PA
15108

Telephone

+18887794372

Website

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May Awareness

May is Huntington’s Disease Awareness Month. Please share your HD story here and support our May events to bring awareness to Huntington’s Disease and find a treatment and cure.