Search results for: awareness month
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…
Read MoreLiving 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…
Read MoreCure 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!…
Read MoreMore 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…
Read MoreGenetic and Rare Diseases Information Center
Looking for current, reliable and easy to understand information about rare or genetic diseases? Contact GARD Information Specialist. Affiliated with the National Institutes of Health (NIH), the Genetic and Rare…
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