Hemophilia Federation of America
Hemophilia Federation of America, Inc. (HFA) is a patient education, services and advocacy organization serving the rare bleeding disorders community. We are exclusively focused on the bleeding disorders patient and caregiver community. We are a community-based organization, committed to championing the needs of families living with chronic, often painful, and debilitating bleeding disorders. We advocate for safe, affordable, and obtainable therapies and health coverage.
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