NHF publishes a monthly newsletter, Community Alert, at no charge, and has numerous brochures that are free if you are requesting one copy. They also provide a new parent packet for parents of newly diagnosed children. The Foundation has a library of journals, books and articles relating to bleeding disorders/HIV that are free to members.
NHF collects information on physicians and researcher who treat/study the condition and disseminates the research information to its members. They operate a toll-free information line that provides referrals and information. They host a national conference, call for further information.
The World Federation of Hemophilia is an international not-for-profit organization dedicated to introducing, improving, and maintaining care for people with hemophilia and related bleeding disorders around the world. The WFH focuses its activities in the following areas:
Through our network of committed volunteers and associated stakeholders, the World Federation of Hemophilia acts as a catalyst to bring about needed change. To this effect, the WFH works with national hemophilia organizations, health care providers, and government officials to foster quality health care for people with bleeding disorders.