The National Hemophilia Foundation (NHF) is dedicated to finding better treatments and cures for inheritable bleeding disorders and to preventing the complications of these disorders through education, advocacy and research. Established in 1948, the National Hemophilia Foundation has chapters throughout the country. Its programs and initiatives are made possible through the generosity of individuals, corporations and foundations as well as through a cooperative agreement with the Centers for Disease Control and Prevention (CDC). NHF awards grants and fellowships to encourage innovative research into finding better treatments and cures for bleeding disorders, as well as to maintain professional excellence in the care of people with bleeding disorders. NHF works to educate and support all people with all bleeding disorders through in-person education, outreach to undiagnosed women, and advocacy for access to care.
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