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About HFA

Hemophilia Federation of America (HFA) is the national community-based advocacy organization serving all people living with bleeding disorders and their families across the United States.

Incorporated in 1994 as a non-profit 501(c)(3) organization, HFA serves as a consumer advocate for safe, affordable, and obtainable therapies and health coverage, as well as a better quality of life for all persons with bleeding disorders.

What is HFA?


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Assisting and Advocating for the Bleeding Disorders Community