Over 450 advocates from around the country gathered in Washington D.C. for NHF’s Annual Washington Days. This year our travel grant recipients and their families advocated for Congress to continue to support the funding for the federal hemophilia programs through the...
Don Smith’s parents were caught completely off guard when he was diagnosed with hemophilia A, severe factor VIII deficiency. Growing up without a family history of bleeding disorders, Don and his family “found themselves in the deep end of a pool of mystery!” His...