The Hemophilia Federation of America (HFA) is a non-profit, 501(c)3 organization incorporated in the spring of 1994 to address a perceived gap in services due to evolving needs of the blood clotting disorders community. We serve as a consumer advocate for safer blood products, affordable and obtainable health insurance coverage, and a better quality of life for all persons with bleeding disorders.

HFA maintains a strong presence in Washington. We utilize the services of the Health and Medicine Counsel of Washington (HMCW), a well established lobbying firm, to insure constant communication of the blood clotting disorders community’s specific concerns with federal agencies and Congress. HFA officers and staff testify before the FDA, CDC, on Capitol Hill and throughout the country to promote blood safety and availability and to address reimbursement, lifetime caps, and other community issues.


Hemophilia Federation of America (HFA)