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/TakeAc
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