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Last September, scientists, doctors, advocates and people with hemophilia gathered in Washington, DC, for the National Hemophilia Foundation’s (NHF) 15th...
For years, researchers studying the bleeding disorders community have sought answers to questions about people’s experiences that only community voices...
In May 2018, more than 200 people representing scientific researchers, hemophilia patients, advocates, clinicians and the pharmaceutical industry gathered in...
Brian Ragaishis is a high school senior in New York City who was diagnosed with von Willebrand disease at age...

NHF’s 75th Anniversary

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