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Ways to Donate

…over 30 years, the support of donors like you has funded the most innovative scientific research, driven our advocacy and awareness efforts, and helped us create more than 25 Centers…

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Living With HHT

…better understand the disease. One of these efforts includes translating the Living with HHT book by Sara Palmer, PhD to Arabic, which will help raise awareness about HHT. He is…

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Cure HHT Social Media Channels

Get the lastest information on everything HHT — clinical trials, educational events, regional awareness activities, revised clinical guidelines, COVID-19 updates and so much more. Stay connected with Cure HHT!…

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More Than a Nosebleed: HHT

Hereditary Hemorrhagic Telangiectasia (HHT) is a genetic condition affecting up to 1.4 million people worldwide. HHT is treatable, but no cure is yet available. Watch this video to learn about…

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