JML Fellowship Awardees
The first-ever recipients of the Jeanne Marie Lusher Fellowship are announced.
Collins Comments on Gene Therapy
In a blog post, NIH Director Dr. Francis Collins says that "Gene therapy represents a possible cure for hemophilia A."
SNF Access Act Becomes Law
The Hemophilia SNF Access Act becomes law, thanks to the voices and concerns of NHF and HFA advocates.
Telehealth Awareness Week
NHF becomes an endorsing partner of the first-ever Telehealth Awareness Week.
State of the Science Research Summit
NHF hosts virtual State of the Science Research Summit to help shape the National Research Blueprint
Research Journal Club
NHF launches Research Journal Club to bring researchers and community members together to discuss the latest science and innovative breakthroughs
NHF's New Mission
NHF refocuses its mission statement to reflect a renewed emphasis on research and an expanded scope to include inheritable blood disorders.
Super Seven
NHF hosts a launch party for Super Seven, its new children’s book for kids with rare bleeding disorders.
JML Fellowship Launches
NHF announces that its newest fellowship, named in honor of Jeanne Marie Lusher, will prioritize diverse researchers.