Changes include deferral policies for MSM, those with hemophilia and their partners, and the role of a new national blood surveillance system.
Open conversation can help normalize a child's bleeding disorder.
NHF Nurses' Guide chapter on emergency room care is now available as a PDF.
Study shows higher risk of inhibitors in children using recombinant vs. plasma-derived factor VIII products to treat severe hemophilia A.
NHF's MASAC issues two new documents, one on treatment recommendations and the other on physical therapy guidelines.
FDA approves Baxalta's Vonvendi, the first recombinant von Willebrand factor therapy for patients with VWD.
Rice University researchers confirm the presence of factor VIII in endothelial cells, a potential site for future gene therapy.
NHF and HTCs respond to HRSA's proposed guidance changes on 340B Drug Pricing Program.
NHF and CDC work together to improve inhibitor screening and testing, after data show true prevalence among people with hemophilia.
NHF chapters hit the ball out of the park with a winning 2015 Walk season, raising money and awareness for the bleeding disorders community.
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