NHF in Action

More than 2,800 people in the bleeding disorders community gathered from October 11-13 in Orlando, Florida, to gain valuable knowledge,...Read More
These grants are part of NHF’s increased commitment to funding critical bleeding disorders research.Read More
More than 250 attendees stood with National Hemophilia Foundation (NHF) CEO Val D. Bias as he raised a glass to...Read More
GroupMe. Facebook’s “like” button. Carousell. These are just a few of the innovations that have emerged out of hackathons—collaborative, intensive...Read More
Living with hemophilia with inhibitors is difficult. The inhibitor—a development of antibodies to infused factor product—makes it more difficult to...Read More
On March 9, more than 500 people with bleeding disorders and their families put on their red ties and prepared...Read More
On March 18, nine athletes laced up their sneakers to run 13.1 miles in Manhattan and help people with bleeding...Read More
In September 2017, the National Hemophilia Foundation’s Medical and Scientific Advisory Council (MASAC) adopted updated guidelines for the treatment of...Read More
Gala raises funds and honors outstanding individuals.Read More
The National Hemophilia Foundation’s (NHF’s) 69th Annual Meeting in Chicago began with a message of unity. Reflecting on the battles...Read More
Continued collaboration at venues like this workshop is the key to improving existing therapies and developing a cure for hemophilia.Read More
Nearly every industry that serves the public must change the way it communicates to reach the growing Hispanic population, including...Read More
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Contact HANDI, NHF's resource center for additional information on bleeding disorders.