Hemophilia Federation of America

Hemophilia Federation of America (HFA) is a non-profit 501(c)3 organization incorporated in 1994 to address the evolving needs of the bleeding disorders community through advocacy, education, and support. We work to promote policies that allow individuals and families affected by bleeding disorders to thrive. These include: supporting equitable, expanded access to quality, affordable health coverage; defending access to clinically appropriate treatments and care; addressing affordability challenges (rising OOP costs, limits on copay assistance); and championing blood and product safety.