Community Pulse

Community Pulse

In-depth profiles and stories about people in the bleeding disorders community.

 

In each issue of HemAware , we “Take 5” with people in the bleeding disorders community and spotlight their efforts...
Worldwide, an estimated 1 in 1,000 people have a bleeding disorder. But 75% receive either inadequate treatment or no treatment...
Advocacy is important to people with bleeding disorders. Many chapters have advocacy days, where members visit the state capitol to...
It has been five years since the National Hemophilia Foundation (NHF) launched its Hemophilia Walk program, starting with five walks...
In each issue of HemAware , we “Take 5” with people in the bleeding disorders community and spotlight their efforts...
Thousands will gather at the World Federation of Hemophilia (WFH) 2012 World Congress in Paris from July 8–12 to participate...
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...
More than 180 people gathered May 9 at Astra, a restaurant overlooking the lights of Manhattan’s 59th Street Bridge, as...
The National Hemophilia Foundation (NHF) is pleased to announce that it was awarded the bid to host the World Federation...
In each issue of HemAware , we “Take 5” with people in the bleeding disorders community and spotlight their efforts...
Lori Keels, executive director of the Louisiana Hemophilia Foundation (LHF), had just learned there was a threat of tornadoes across...
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