Watchdog

Watchdog

Obtaining the federal designation of March as Bleeding Disorders Awareness Month was the cornerstone of the National Hemophilia Foundation’s (NHF’s)...
“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...
When Michelle Rice’s older son, Lance, was 5 days old, he had an intra­cranial hemorrhage and spent three weeks in...
Bills that come up for a vote in Washington, DC, often stall as they get defeated repeatedly on the US...
The National Hemophilia Foundation (NHF) is excited to welcome the bleeding disorders community to its 65th Annual Meeting October 3–5...
Being diagnosed with a bleeding disorder can spark a lifetime of questions. As treatments, research, medical protocols and healthcare policy...
It has been five years since the National Hemophilia Foundation (NHF) launched its Hemophilia Walk program, starting with five walks...
For the past three years, patients and their families at the National Hemophilia Foundation’s (NHF) Washington Days advocacy event have...
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Contact HANDI, NHF's resource center for additional information on bleeding disorders.