The World Federation of Hemophilia (WFH) World Congress will be held in the United States for the first time in...

The National Hemophilia Foundation (NHF) conducted a daylong summit of hemophilia stakeholders on May 24, 2012, in Washington, DC, to...

Being diagnosed with a bleeding disorder can spark a lifetime of questions. As treatments, research, medical protocols and healthcare policy...

Advocacy is important to people with bleeding disorders. Many chapters have advocacy days, where members visit the state capitol to...

Attendees at the 2012 National Hemophilia Foundation’s (NHF) Washington Days event received training on advocacy before meeting with their elected...

For the past three years, patients and their families at the National Hemophilia Foundation’s (NHF) Washington Days advocacy event have...

Connect for Bleeding Disorders is the National Hemophilia Foundation’s (NHF) new young professionals group, drawing people from various backgrounds. Members...

Seven years ago, a big gust of wind off the Wyoming plains sent a piece of plywood flying, hitting the...

Approximately 15 social workers from Los Angeles–area hospitals gathered in January at the Hemophilia Foundation of Southern ­California (HFSC) Social...

The National Hemophilia Foundation (NHF) is proud to announce it has won four awards from the American Society of Healthcare...

The National Hemophilia Foundation (NHF) is pleased to announce that it was awarded the bid to host the World Federation...

More than 300 members of the bleeding disorders community gathered in Washington, DC, on March 8 for NHF’s annual advocacy...