Since the World Federation of Hemophilia (WFH) launched the Global VWD Call to Action in 2018, the visibility and awareness of von Willebrand Disease (VWD)...
Salomon is a 10-year old hemophilia A patient who lives in Kenya. He walks a kilometre to school with a donated crutch—even when it rains...
The ASH ISTH NHF WFH guidelines for the management and diagnosis of von Willebrand disease (VWD) are the product of an innovative international collaboration with...
The bleeding disorders community is facing unprecedented challenges. The WFH—and our national member organizations (NMOs) and partners—are all coping with the consequences of the global...
With up to 1% of the World’s population suffering from von Willebrand disease (VWD), it is by far the most common type of bleeding disorder....
Every two years, the WFH recognizes outstanding volunteers who generously share their time, expertise, energy—and deep and longstanding commitment—with the global bleeding disorders community. This...
The following is the first in a 3-part series about how NMOs in the Middle East region have responded to the coronavirus disease 2019 (COVID-19)...
It’s official! Registration for the WFH Virtual Summit: Connecting the Global Bleeding Disorders Community is now open. The Virtual Summit—which is free—will feature a series...
The World Federation of Hemophilia (WFH) is monitoring the manufacturing, safety and supply of hemophilia therapies during the coronavirus pandemic. The WFH will be posting all...
The April 2020 issue of Haemophilia, the official journal of the World Federation of Hemophilia (WFH), includes a section for researchers in developing countries who...