This past July featured a first in the world of bleeding disorders: back-to-back meetings. First, the National Hemophilia Foundation’s (NHF’s)...

Megan Adediran didn’t understand what was happening. After her son was born, he bled for five days after circumcision. A...

Hosted by the National Hemophilia Federation (NHF), the upcoming World Federation of Hemophilia (WFH) 2016 World Congress is expected to...

When the World Federation of Hemophilia (WFH) announced that a donation of 500 million units of factor had been made...

The US bleeding disorders community will welcome the world to the 2016 World Federation of Hemophilia’s (WFH’s) World Congress in...

Every year on April 17, World Hemophilia Day is observed around the world to increase awareness of hemophilia and other...

The World Federation of Hemophilia (WFH) supports its goal of treatment for all through many programs, including Advocacy in Action...

Since 2007, the World Federation of Hemophilia (WFH) has awarded the WFH Susan Skinner Memorial Fund Scholarship to young women...

On April 17, 2014, the global bleeding disorders community joined together to celebrate World Hemophilia Day. It was a day...

With our shared history, the World Federation of Hemophilia USA (WFH USA) and the Foundation for America’s Blood Centers (FABC)...

One of the greatest challenges in trying to improve the lives of people with bleeding disorders in developing countries is...

The World Federation of Hemophilia’s (WFH’s) 2014 World Congress, the largest international meeting dedicated to hemophilia, von Willebrand disease, rare...