WFH: Report on the Annual Global Survey 2015 now available

Christine Herr, Data and Research Coordinator The Report on the Annual Global Survey 2015 is now available in print and online at www.wfh.org/globalsurvey. The report includes selected demographic and treatment-related data on people throughout the world with hemophilia (PWH), von Willebrand disease (VWD), other rare factor deficiencies, and inherited platelet disorders. The Report on the Annual Global Survey 2015 is […]

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WFH – Recipients Double As the WFH Humanitarian Aid Program Expands

Recipients Double As the WFH Humanitarian Aid Program Expands World Federation of Hemophilia – Oct 05, 2016   MONTREAL, Canada – October 5, 2016 – One year following the expansion of the World Federation of Hemophilia (WFH) Humanitarian Aid Program, the number of recipient countries went from 58 to 63, while delivered donations reached a landmark of 100 million international units (IU), […]

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NEWS – WFH Congress 2016 – President: Education is the other side of “Treatment for All” equaition

WFH president: Education is the other side of the Treatment for All equation   Jul 26, 2016 In 1942, The Little Prince author Antoine de Saint Exupery wrote to a friend: “Far from hurting you, being different enriches you.” Nearly 75 years later, it’s still important for everyone in the bleeding disorders community to reflect on that truism, said Alain Weill, WFH […]

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World Federation of Hemophilia

www.wfh.org     World Federation of Hemophilia: Cornerstone of global development For over 50 years, the World Federation of Hemophilia (WFH) has provided global leadership to improve and sustain care for people with inherited bleeding disorders, including hemophilia, von Willebrand disease, rare factor deficiencies, and inherited platelet disorders.   We save and improve lives by: Training experts in the field […]

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