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.

Cuando los miembros de la iglesia de la infancia de Sasha Cheatham en Oklahoma supieron que su hijo pequeño había...
When one of its own was diagnosed with hemophilia, an Oklahoma congregation sprang into action.
La comunidad de trastornos hemorrágicos tiene la fortuna de recibir el apoyo de muchas personas que no tenían una conexión...
People with no prior connection to bleeding disorders become passionate advocates.
NHF held its 5th annual Spring Soiree on May 21, 2015. The more than 200 guests gathered to celebrate the...
The passage of the Patient Protection and Affordable Care Act (ACA) in 2010 signaled a time of promise for those...
Registration is now open for the National Hemophilia Foundation’s (NHF’s) 2012 Inhibitor Education Summits, educational conferences for people who have...
The definition of the word “inhibit” is “to prohibit from doing something.” But the approximately 550 attendees at the 2011...
First Step, the first component of the National Hemophilia Foundation’s (NHF’s) Steps for Living, a new Web-based, comprehensive education program...
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...
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