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).
National Hemophilia Foundation Resources
Basics of Bleeding Disorders
Genetics of Bleeding Disorders
First Step (Birth-8)
Next Step (9-15)
Step Up (16-25)
Step Out (Adults)
Contact NHF’s Information Resource Center
Locate a Camp Near You
NHF’s Chapter Directory
Hemophilia Treatment Center Directory
Personal Health Insurance Toolkit
Steps for Living Downloadable Resources
This One Time at Camp
Making Your Clotting Factor Work for You: Understanding Half-Life in Your Life
Hemophilia Treatment Center: More Than Just a Treatment Center
Bleeding Disorders in the Workplace
What is VWD?
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