Fighting for You

I have been the executive director of the Virginia Hemophilia Foundation (VHF) for nearly 10 years. It has been tremendously...Read More

The National Hemophilia Foundation (NHF) commends the US Food and Drug Administration (FDA) for initiating development of a national blood...Read More

When a person with hemophilia seeks medical care outside his or her hemophilia treatment center (HTC), most likely the physician...Read More

Nearly two decades ago I joined a team of researchers, mostly comprising physician-scientists, to help develop a gene therapy for...Read More

Nearly 350 members of the bleeding disorders community gathered in Washington, DC, February 24–27, 2015, for NHF’s annual advocacy event,...Read More

The bleeding disorders community is a diverse one: There are parents ­startled by the diagnosis of an unexpected disorder in...Read More

What do a TV star, a juggler and a mock candidate for president of the United States have in common?...Read More

Social media has long been lauded for its ability to connect people with common interests, regardless of their location. When...Read More

Kyle Brown is fortunate that his hemophilia treatment center (HTC) kept ordering his medications. Ideally, his prophylaxis supply should have...Read More

It was December 1984, and Ryan White was a middle school student in Kokomo, Indiana. He’d just learned during hemophilia...Read More

In January, the National Hemophilia Foundation (NHF) announced the dedication of the NHF/Novo Nor­disk HANDI Library with a ribbon-cutting ceremony...Read More

On April 28, on the banks of the Hudson River, the National Hemophilia Foundation (NHF) welcomed 250 people to its...Read More