Hemophilia Federation of America (HFA)
Hemophilia Federation of America (HFA) is a patient education, services, and advocacy non-profit 501(c)3 organization incorporated in 1994 to address the evolving needs of the rare bleeding disorders community. We exclusively focus on the bleeding disorders patient and caregiver community. Our member organizations across the country utilize HFA’s collaborative federation to strengthen community support and awareness, develop effective local organizations, and implement valuable programs.