NHF in Action

Read the latest updates out of the National Hemophilia Foundation.

Chapter leaders pictured with NHF CEO Val D. Bias
Programs and Services Award Presented to chapters that excel in providing programs and services to their communities. • Bleeding Disorders...
Jacey Gonzalez, Jeanne White-Ginder and NHF CEO Val D. Bias
Every year, the National Hemophilia Foundation (NHF) honors some of the brightest stars in the bleeding disorders community. From providers...
Sue Martin saves her speech for posterity in the NHF time capsule, which will be opened in 30 years during the 100th NHF Bleeding Disorders Conference.
More than 2,800 people in the bleeding disorders community gathered from October 11-13 in Orlando, Florida, to gain valuable knowledge...
Researcher holding test tube of blood
These grants are part of NHF’s increased commitment to funding critical bleeding disorders research.
Milo Cedeno and Michael Tarantino, MD at the NHF Red Tie Soiree held May 9 at Current at Chelsea Piers in New York
More than 250 attendees stood with National Hemophilia Foundation (NHF) CEO Val D. Bias as he raised a glass to...
A team of hackers at the Hacking Hemophilia event at MIT in October 2017
GroupMe. Facebook’s “like” button. Carousell. These are just a few of the innovations that have emerged out of hackathons—collaborative, intensive...
The Williams family of Tallahassee, Florida, at one of NHF's Inhibitor Summits.
Living with hemophilia with inhibitors is difficult. The inhibitor—a development of antibodies to infused factor product—makes it more difficult to...
Boy talks with Congressional staffer during NHF's Washington Days 2018
On March 9, more than 500 people with bleeding disorders and their families put on their red ties and prepared...
Team NHF's Half-Marathon Team
On March 18, nine athletes laced up their sneakers to run 13.1 miles in Manhattan and help people with bleeding...
Updated NHF guidelines aim to improve emergency care
In September 2017, the National Hemophilia Foundation’s Medical and Scientific Advisory Council (MASAC) adopted updated guidelines for the treatment of...
Daniela Delgado and her parents.
Gala raises funds and honors outstanding individuals.
The bleeding disorders community gathered in Chicago for NHF's 69th Annual Meeting in August 2017
The National Hemophilia Foundation’s (NHF’s) 69th Annual Meeting in Chicago began with a message of unity. Reflecting on the battles...
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