Novel Technologies

Novel Technologies

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.
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...
All of the funding for the JGP program comes from donations from NHF chapters and individuals.
We strive toward enrolling 2,000 confirmed hemophilia carriers in the MLOF Research Repository.
Like hepatitis C, hepatitis B is a viral infection in the liver. The infection can be acute or chronic, in...
The most common inherited bleeding disorder, von Willebrand disease (VWD) has also been one of the most difficult to diagnose...
Two subcutaneous therapies are currently being investigated.
MLOF is open to all people with hemophilia A and B.
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Contact HANDI, NHF's resource center for additional information on bleeding disorders.