Community in Action

On a rainy Saturday in January, 26 people arrived at Valley Children’s Hospital (VCH) in Madera, CA, for one reason:...Read More
They’re the rarest of the rare: bleeding disorders like platelet storage pool disorder and factor XIII deficiency that affect only...Read More
NHF held its 5th annual Spring Soiree on May 21, 2015. The more than 200 guests gathered to celebrate the...Read More
The passage of the Patient Protection and Affordable Care Act (ACA) in 2010 signaled a time of promise for those...Read More
Barry Haarde completed a 3,700-mile bike ride from Oregon to New Hampshire in August 2012, as part of the Ride...Read More
Registration is now open for the National Hemophilia Foundation’s (NHF’s) 2012 Inhibitor Education Summits, educational conferences for people who have...Read More
With exotic bird cries filling the air, more than 600 participants in the Florida Hemophilia Association (FHA) Walk meandered down...Read More
The definition of the word “inhibit” is “to prohibit from doing something.” But the approximately 550 attendees at the 2011...Read More
First Step , the first component of the National Hemophilia Foundation ’s (NHF’s) Steps for Living , a new Web-based,...Read More
HemAware magazine and its Web site, , are bringing home the gold, winning top honors from several publishing organizations.Read More
The National Hemophilia Foundation (NHF) is pleased to announce the appointment of Marion A. Koerper, MD, as its medical advisor....Read More
Susan Scroggins didn’t know which was worse: that both her children had been diagnosed with type 1 von Willebrand disease...Read More
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Contact HANDI, NHF's resource center for additional information on bleeding disorders.