The National Hemophilia Foundation (NHF) is a United States patient advocacy organization for the care and treatment of inheritable blood and bleeding disorders such as hemophilia and von Willebrand disease. Founded in 1948, the NHF helps secure funding for treatment centers, and develops national guidelines for treatment and health care policy. The organization also serves as a central point for information on the disorders. The National Hemophilia Foundation was founded in 1948, as the first national hemophilia advocacy organization in the United States. One of its early initiatives was to secure funding for Comprehensive Hemophilia Diagnostic and Treatment Centers (HTC). More information...

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