Hemophilia Federation of America (HFA)

Hemophilia Federation of America, Inc. (HFA) is a patient education, services and advocacy organization serving the rare bleeding disorders community. They are exclusively focused on the bleeding disorders patient and caregiver community.

HFA is a non-profit 501(c)(3) organization incorporated in 1994 to address the evolving needs of the bleeding disorders community. HFA serves as a community-based organization, committed to championing the needs of families living with chronic, often painful, and debilitating bleeding disorders. They advocate for safe, affordable, and obtainable therapies and health coverage. Ultimately, they seek a better quality of life for all persons with bleeding disorders.

Vision
The vision of Hemophilia Federation of America is to improve the care and quality of life for all people with bleeding disorders by removing barriers to diagnosis, treatment, and cure.

Mission Statement
Hemophilia Federation of America is a national nonprofit organization that assists, educates, and advocates for the bleeding disorders community