Hemophilia Federation of America: Assisting and Advocating for the Bleeding Disorders Community

Welcome to HFA

The 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. We serve as a consumer advocate for safe, affordable, and obtainable blood products and health coverage, as well as a better quality of life for all persons with bleeding disorders.

Our Mission

The Hemophilia Federation of America is a national nonprofit organization that assists and advocates for the bleeding disorders community.

Our Vision

The vision of the Hemophilia Federation of America is that the bleeding disorders community has removed all barriers to both choice of treatment and quality of life.

http://www.vimeo.com/5343876

The Voices Campaign is HFA’s grassroots advocacy initiative aimed at raising general public and legislator awareness of the bleeding disorders community through personal stories from affected individuals and their families. In the approaching national debates regarding health care reform, HFA wants to ensure the bleeding disorders community is heard, and through the Voices Campaign, members of the community can learn how to better advocate for the community through effective sharing of personal stories.