We invite you to join the quarterly board of directors meeting for the National Hemophilia Foundation on May 18th starting at 7:00 pm ET. This meeting will discuss NHF business operations and decisions and is…
The Rare Diseases Diversity Coalition (RDDC) is currently seeking applicants for its 2023 Rare Disease Fellowship Program, which is aimed at inspiring the next generation of the medical workforce to work in the rare disease space and…
Every day, chapters across the country work with the blood and bleeding disorders community around them. Since 2021, Jacob Murdock has served as Chapter Executive Director in Nevada. He took time out of his busy schedule to tell us why loves the…
When Saylor Behrens' biology professor told her class that hemophilia is the result of incest, she grew angry. She knew better. Her younger brother, Wyatt, has hemophilia A.
It wasn't just the false narrative being spread that made her indignant…
Dear National Hemophilia Foundation Community, Staff and Friends,It is with mixed emotions that I want to inform you that I have decided to step down from my leadership position as President and CEO at the end of this year. Earlier this week, I…
Managing Pregnant Women with Hemophilia and von Willebrand Disease: How Do We Provide Optimum Care and Prevent Complications?
Speaker: Dr. Maissaa Janbain
NHF's Wednesday Webinars are a free education series open to providers…
Hemophilia Gene Therapy: First, Do No Harm
Speaker: Dr. Len Valentino
NHF's Wednesday Webinars are a free education series open to providers and community members. Register to attend and learn about the latest in research,…