Hereditary Hemorrhagic Telangiectasia – Osler-Weber-Rendu

Tag Archive for ‘Congress’

HHT Awareness Video

The HHT Foundation is proud to announce our first HHT Awareness initiative …. the video production More Than A Nosebleed: HHT. We all have our own HHT story and path to diagnosis but Bernstein-Rein, an advertising agency, through patient stories and the medical expertise of three HHT Center of Excellence Directors, has created the most [...]

HHT Authorization Bill Introduced to Congress

HHT Diagnosis and Treatment Act of 2011 – U.S. House of Represenatives H.R. 2123 and U.S. Senate Bill S.1167. We need as many Co-Sponsors in the House and Senate as possible. It is critical for you to contact your Senators and House Representative and ask them to Co-Sponsor these bills.