Community Pulse

Community Pulse

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

 

These grants are part of NHF’s increased commitment to funding critical bleeding disorders research.
More than 250 attendees stood with National Hemophilia Foundation (NHF) CEO Val D. Bias as he raised a glass to...
In March, bleeding disorders advocates nationwide donned their red ties and raised a record-setting amount of money during the National...
I was diagnosed with von Willebrand disease (VWD) three days after I was born, 25 years ago. A vitamin K...
One of the probably lesser known—and certainly most far-flung—of the 140-plus federally designated US hemophilia treatment centers (HTCs) will soon...
Juniata College is a small liberal arts school in Huntingdon, Pennsylvania, about 125 miles east of Pittsburgh. The college was...
GroupMe. Facebook’s “like” button. Carousell. These are just a few of the innovations that have emerged out of hackathons—collaborative, intensive...
Living with hemophilia with inhibitors is difficult. The inhibitor—a development of antibodies to infused factor product—makes it more difficult to...
On March 9, more than 500 people with bleeding disorders and their families put on their red ties and prepared...
On March 18, nine athletes laced up their sneakers to run 13.1 miles in Manhattan and help people with bleeding...
Clinical trials provide important information about how well drugs and devices work and how safe they are, but they’re not...
“The threat to the life of just one hemophiliac would be sufficient reason for us to travel to this meeting...
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