The World Federation of Hemophilia (WFH) is an international non-profit organization dedicated to improving the lives of people with hemophilia (also spelled haemophilia) and other genetic bleeding disorders. It educates people with bleeding disorders and lobbies for improved medical treatment.[4][5] 75% of people in the world with bleeding disorders do not know it and do not receive care.[6][7]
^Raabe, Michelle (2008). Hemophilia. Infobase Publishing. p. 123. ISBN978-0-7910-9648-2. The WFH is an international, not-for profit organization that works to improve standards of treatment, promote advocacy, provide education, and advance medical research concerning hemophilia.
^Venkataraman, Lakshmi (16 April 2019). "World Hemophilia Day - Reaching Out". Medindia. Retrieved 2023-04-18. World Hemophilia Day 2019 aims to reach out as far and wide as possible to ensure proper diagnosis and treatment to nearly 75 percent of patients who still remain undiagnosed or don't have access to treatment.
^"Fast Facts". National Hemophilia Foundation. 2014-03-04. Retrieved 2020-04-16.