Fighting For You

Fighting for You

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...
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...
Nearly 350 members of the bleeding disorders community gathered in Washington, DC, February 24–27, 2015, for NHF’s annual advocacy event...
The bleeding disorders community is a diverse one: There are parents ­startled by the diagnosis of an unexpected disorder in...
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