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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.

Alizée Palomba

Cure HHT’s 2024 Impact Report

A Year Of Significant Transformation & Progress Every year is a different chapter in our story – each bringing us closer to our ultimate goal.....
Friday, Cassi

Your donations do more than you may realize

Hi! For those who may not know me, I'm Cassi Friday and I’m the Director of Research here at Cure HHT. That’s not the only...
Photograph of a young girl named Harper smiling in front of a white board that says "Congrats Harper" with a drawing of lungs

More Than A Nosebleed: In Loving Memory of Harper

Turning two-years old comes with many changes— from growth spurts to a surging vocabulary. But as her little Harper grew, Rebecca Newman noticed a concerning...

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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