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Since Cure HHT was established 25 years ago, we have been dedicated to providing answers to every question we can about HHT for patients, caregivers, doctors and researchers. Cure HHT remains the primary source for the most recent and reliable information about Hereditary Hemorrhagic Telangiectasia.

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HHT: A Whole System Disease

HHT is often introduced to the world through a single symptom — nosebleeds. But HHT is never only one thing. It is a whole system...
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Invitation: 2025 HHT Patient and Physician National Conference

I’m so excited to introduce myself to this amazing community. My name is Hellen Tecle, and I stepped into the role of Manager of Community...
Cure HHT Leads Global Breakthrough in Bleeding Standards, Paving the Way for Future HHT Therapies

Cure HHT Leads Global Breakthrough in Bleeding Standards, Paving the Way for Future HHT Therapies

A newly published international consensus report—developed under the leadership of Cure HHT, the only nonprofit organization in the world dedicated to funding global research, awareness,...

Cure HHT is happy to provide a wide array of resources for patients, families, physicians and researchers. Be sure to check out our extensive resource library that houses fact sheets, brochures, publications, and all of our educational webinars.

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With an entire team of dedicated specialists to coordinate care, the HHT Treatment Centers of Excellence are the best place to access expert HHT care.

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See what webinars we have coming up so you can watch them LIVE and get your questions answered in real time! You can also view our past webinars, with topics including (but not limited to!) insurance, AVMs, research, genetics, and children with HHT.

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