News
Cure HHT Canada Launches as Part of a Growing International Commitment to HHT Care, Research, and Advocacy
Newly strengthened organization will work alongside Cure HHT to improve diagnosis, care, and connection for the Canadian HHT community Cure HHT is proud to announce [...]
Donald’s Story: What We Know Can Save a Life
From his earliest memories, Donald remembers nosebleeds. They were simply part of life. His mother had them. Some of [...]
Webinar: Brain AVMS – Recent Advances in Imaging and Management
In this session Dr. Krings will describe recent advances in imaging, neurointervention and medical management in patients with Brain Arteriovenous Malformations. In particular he will discuss how Vessel Wall Imaging allows us to understand why certain brain AVMs bleed and how to predict future rupture. He will discuss in [...]
Join us at the 16th HHT International Scientific Conference
16th HHT International Scientific Conference Where Breakthroughs Set Sail October 12–16, 2026 | Cape Cod, Massachusetts Charting the Future of HHT Care—Together Progress in hereditary hemorrhagic telangiectasia begins with collaboration. This international conference brings together clinicians, researchers, scientists, industry partners, and advocates from around the world to share breakthroughs, [...]
Hereditary Hemorrhagic Telangiectasia (HHT), also known as Osler-Weber-Rendu Syndrome, is an inherited disease that leads to malformed blood vessels in multiple organs of the body.
The disease typically begins with nosebleeds during childhood, and can result in serious health problems if not promptly diagnosed and treated. Our mission is to find a cure for HHT while saving the lives and improving the well-being of individuals and families affected by HHT.
Cure HHT Canada is a charity that is committed to supporting individuals and families affected by hereditary hemorrhagic telangiectasia (HHT). By raising funds for HHT research and to advance the care of this disease, our aim is to become a hub for HHT awareness and education across Canada. We invite you to browse our site to learn more about HHT and the care that is available in Canada. This site contains information for Canadians with HHT, concerned family members and clinicians involved in the care of patients with HHT.
