Camp Wilderness is our most beloved and anticipated program held every summer for kids ages 7-17 diagnosed as carriers, with hemophilia, von Willebrand disease, and/or platelet disorders. Camp is a…
In 2020 NHF began an exciting collaboration with a number of blood disorder groups who receive funding from the Centers of Disease Control and Prevention. The focal point of this collaboration is a series of public health-minded educational sessions…
As the eyes of the world fix upon Ukraine, I am shocked and saddened to see heartbreaking images emerge showing injured civilians staggering through the streets and towns in the east of the country following Russian bombing over the last several…
Dr. Johnny Mahlangu graciously sat down with NHF's CEO Dr. Len Valentino for an informative dialogue to honor Black History Month and World Hemophilia Day. Read these Q&As and watch the video to learn more!
Black History Month and…
NBDF encourages redistribution of its publications for educational purposes by other nonprofit bleeding disorders organizations. NBDF produced materials, either printed publications or website content, cannot be translated or reproduced in whole or…
We invite you to join the quarterly board of directors meeting for the National Hemophilia Foundation on March 3rd starting at 7:00 pm ET. This meeting will discuss NHF business operations and decisions and is open…
Hepatitis C Virus in Hemophilia: Health-related Quality of Life After Successful Treatment
Speaker(s): Dr. Cas Isfordink and Dr. Samantha Gouw
Did you miss the March 9th Wednesday Webinar? If so click here to…
Breakthrough Bleeding Episodes in Pediatric Severe Hemophilia a Patients with and without Inhibitors Receiving Emicizumab Prophylaxis: a Single-center Retrospective Review
Speaker(s): Dr. Eman Hassan
Dr. Eman…