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The World Federation of Hemophilia (WFH) is committed to bringing the bleeding disorders community together in the name of Treatment for All. This commitment is especially important during the COVID-19 crisis. The WFH deeply believes that where you live should not determine your access to care and treatment for an inherited bleeding disorder.
Our vision of Treatment for All is that one day, all people with a bleeding disorder will enjoy a more certain future filled with promise, no matter where they live. The mission of the WFH is to improve and sustain care for people with inherited bleeding disorders around the world. In order to achieve this, we actively pursue long-term relationships with individuals and organizations who share the values inherent in our comprehensive development model.
We work to ensure every person—including those living with hemophilia and von Willebrand disease (VWD), those with rare factor deficiencies, and women with bleeding disorders—have access to world-class care and recognition of their condition. Our corporate partners, donors, and volunteers all share this belief and we thank them for their past and ongoing contributions.