Global

When Yuri Zhulyov began his work with the bleeding disorders community in 1989, the number of people living with hemophilia in Russia was unknown.

The World Federation of Hemophilia is developing a program to facilitate international collaboration in research.

Wear red? Chalk it on the sidewalk? Tweet it? How did you share your story and celebrate World Hemophilia Day on April 17?

“The launch of the GAP project is good news that without doubt brings hope to tens of thousands of people with hemophilia living in China.”

Hemophilia is one of the most expensive diseases to treat in Taiwan, but the Hemophilia Association of Taiwan does not want its community to become complacent about its national health insurance benefits.

The World Federation of Hemophilia’s Twinning Program links emerging and established hemophilia organizations and treatment centers.

A child and his mother travel for a week by bus in Peru to visit a treatment center. A young man from rural Armenia has a leg amputated—the result of a lack of available factor concentrates.

The World Federation of Hemophilia distributes donated clotting factor concentrates to patient organizations in more than 50 countries.