Uncategorized

The Centers for Disease Control and Prevention (CDC) and the National Hemophilia Foundation (NHF) are seeking teens ages 16-19 to participate in group discussions about living with with bleeding [...]

The New York City Hemophilia Walk is just five weeks away and we need your help now more than ever! Can your company be a sponsor? Can you start or […]

With current treatments, the vast majority of individuals with hemophilia can live long, fulfilling lives. However, better treatments are not a cure. Many still deal with the immune response to [...]

The U.S. Food and Drug Administration (FDA) has approved Corifact™, a plasma-derived factor XIII product, for the routine prophylactic treatment of congenital factor XIII (FXIII) deficiency. The [...]

On April 17th, communities around the globe will observe World Hemophilia Day, a time to remember that many with bleeding disorders still lack adequate care. Learn more by visiting www.wfh.org.

The crisis in Japan serves as a reminder that emergency situations can happen at any time. However, there are simple things that any family or individual can do to prepare […]

The World Federation of Hemophilia (WFH) is conducting a survey asking consumers and their families, about their perceptions of the challenges of conducting clinical research in hemophilia [...]

Albany Hemophilia Days, an annual grassroots advocacy effort at the New York State Capitol, will take place on Sunday and Monday, March 6-7, 2011. Families and individuals affected by bleeding [...]

For Immediate Release Please Contact: Jeri Krassner, Manager at (917) 597-7256 [email protected] New York City Hemophilia Chapter Announces New LeadershipGlenn Mones Named Executive [...]

Washington Days, NHF’s annual grassroots advocacy day on Capitol Hill, will take place from February 16-18, 2011. This is your opportunity to learn about key legislative issues affecting [...]