HANDI, NHF’s information resource center, answers requests for information. If you’ve got questions, they’ve got answers.
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Community Resources
Here you will find everything from the National Hemophilia Foundation’s HANDI Information Resource Center to camp and chapter directories, and a list of publications.
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HANDI, NHF's Information Resource Center
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Hemophilia Treatment Centers Near You
Hemophilila treatment centers are specialized healthcare centers that bring together a team of doctors, nurses, and other health professionals experienced in treating people with bleeding disorders.
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Chapter Directory
Connect with other families affected by bleeding disorders in your area through NHF's chapter network.
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Other Bleeding Disorder Organizations
Find a helpful list of bleeding disorders organizations, along with their contact information.
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Clinical Trials
Learn more about clinical research and new medical therapies for treating hemophilia and related conditions.
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Scholarships
Students should apply now for academic scholarships with May and June deadlines, including the Kevin Child Scholarship.
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HemAware
HemAware, the National Hemophilia Foundation’s award-winning quarterly magazine, is the bleeding disorders community’s premier lifestyle publication. It features stories on research breakthroughs, family concerns, exercise and nutrition, women’s health needs and life stage transitions.
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Making Knowledge Hereditary: My Life, Our Future
Get genotyped, and bring your family too! Gain a deeper understanding of your hemophilia today, while helping to advance the breakthrough treatments of tomorrow.
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Women with Bleeding Disorders
Although hemophilia is thought of as a man’s bleeding disorder, women can have it, too.
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My Hemophilia Team
MyHemophiliaTeam is a free, secure social network where you can connect with others in the hemophilia community on your phone, tablet or computer.