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.
Hemophilia Federation of America (HFA) member organizations across the country utilize HFA’s collaborative federation to strengthen community support and awareness, develop effective local organizations, and implement valuable community-based programs.
The World Federation of Hemophilia improves and sustains care for people with inherited bleeding disorders around the world.
Comprehensive Health Education Services (CHES) is dedicated to the education and nurturing of individuals with bleeding disorders, their families, and their medical professionals.
The Coalition for Hemophilia B strives to make quality of life the focal point of treatment for people with hemophilia B and their families through education, empowerment, advocacy, and outreach.
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