Research and Treatment

Research & Treatment

In December 2015, Ryan Hallock did something that changed his life: He became the first patient treated in a gene...
From academia to industry to advocacy, the National Hemophilia Foundation’s new president and CEO, Leonard Valentino, MD, has done it...
Telemedicine can bridge the distance between doctor and patients.
Last September, scientists, doctors, advocates and people with hemophilia gathered in Washington, DC, for the National Hemophilia Foundation’s (NHF) 15th...
In May 2018, more than 200 people representing scientific researchers, hemophilia patients, advocates, clinicians and the pharmaceutical industry gathered in...
Welcoming a new NHF-Shire clinical fellow.
NHF-Shire Clinical Fellowship Program award recipients are committed to bleeding disorders clinical care and research.
Advances in bleeding disorders care rely on research, but is taking part in a study right for you?
Assessing the My Life, Our Future Genotyping Project A recent article in the journal Haemophilia analyzed the My Life, Our...
On February 23 and 24, an international group of researchers from universities, industry and government gathered in Washington, DC, for...
These grants are part of NHF’s increased commitment to funding critical bleeding disorders research.
All of the funding for the JGP program comes from donations from NHF chapters and individuals.
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Contact HANDI, NHF's resource center for additional information on bleeding disorders.