Community-Voices

Community-Voices

People with blood or bleeding disorders and their family members are at the heart of the National Hemophilia Foundation. Read in-depth profiles and stories about people in the bleeding disorders community.

HemAware magazine and its Web site, hemaware.org, are bringing home the gold, winning top honors from several publishing organizations.
The National Hemophilia Foundation (NHF) is pleased to announce the appointment of Marion A. Koerper, MD, as its medical advisor...
Susan Scroggins didn’t know which was worse: that both her children had been diagnosed with type 1 von Willebrand disease...
Chicago, the “city of big shoulders,” will embrace the bleeding disorders community for the National Hemophilia Foundation’s (NHF’s) 63rd Annual...
When I became the executive director of the Colorado Chapter of the National Hemophilia Foundation (NHF) in December 2010, it...
The Rally Concludes July 21, 2011
“You catch a fish, you kiss the fish, and then you throw it back,” explains Janet Brewer, MS, CEO of...
Living with hemophilia and an inhibitor can be isolating; people with inhibitors constitute a small portion of an already small...
Kevin Child was one month short of college graduation when he died of complications from AIDS in 1989. In his...
The National Hemophilia Foundation’s (NHF’s) Annual Meeting is the organization’s flagship event. It provides educational sessions for people with bleeding...
National Hemophilia Foundation CEO Val D. Bias and New York City nightlife photographer Patrick McMullan called attention to women’s bleeding...
I anticipated my first National Hemophilia Foundation (NHF) Annual Meeting with a lot of excitement, but without many expectations. My...
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