Fighting For You

Fighting for You

Against a backdrop of a possible repeal of the Affordable Care Act (ACA), the National Hemophilia Foundation’s (NHF) Washington Days...
The minimum amount of clotting factor a country requires to avert death in life-threatening instances is 1 international unit (IU)...
More than a quarter of the bleeding disorders population in the US relies on Medicaid to pay health expenses. Changes...
Obtaining the federal designation of March as Bleeding Disorders Awareness Month was the cornerstone of the National Hemophilia Foundation’s (NHF’s)...
On May 19, 2016, more than 200 people gathered at Current at Chelsea Piers to celebrate the honorees of the...
Efforts to raise awareness of health conditions have gotten more creative. The Ice Bucket Challenge brought prominence to the condition...
The National Hemophilia Foundation (NHF) has been advocating for the bleeding disorders community and holding advocacy days in Washington, DC...
“THINK BETTER. THINK BIGGER. THINK BEYOND.”These are the themes Steven W. Pipe, MD, laid out in summer 2015 as part...
I have been the executive director of the Virginia Hemophilia Foundation (VHF) for nearly 10 years. It has been tremendously...
The National Hemophilia Foundation (NHF) commends the US Food and Drug Administration (FDA) for initiating development of a national blood...
When a person with hemophilia seeks medical care outside his or her hemophilia treatment center (HTC), most likely the physician...
Nearly two decades ago I joined a team of researchers, mostly comprising physician-scientists, to help develop a gene therapy for...
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Contact HANDI, NHF's resource center for additional information on bleeding disorders.