Advocacy

Advocacy

HemAware has everything you need to know about inheritable blood and bleeding disorders. Together, we fight for access to healthcare. Read now to learn more.

Hemophilia and von Willebrand disease (VWD) are not well-known outside the bleeding disorders community. But thanks to the spotlight on...
“Never doubt that a small group of thoughtful, committed citizens can change the world. Indeed, it is the only thing...
Despite hemophilia’s very visible symptoms—bleeding and bruising— the disorder has been a hidden one for a long time.
Betty Jane Henry died at her home in Wellington, Florida, on Sunday, September 5, at the age of 93. She...
Lisa and Michael Louwers are both doctors, but the Farmington Hills, Michigan, couple didn’t know much about hemophilia or other...
The US Department of Health and Human Services has unveiled Healthy People 2020, the nation’s new 10-year goals and objectives...
At the Opening Session of the National Hemophilia Foundations’s (NHF's) 62nd Annual Meeting in New Orleans on November 11, 2010...
While national healthcare reform passed in March, implementing it will occur in stages. The legislation is detailed and has many...
In each issue of HemAware, we “Take 5” with people in the bleeding disorders community and spotlight their efforts with...
A select group of hemophilia community leaders visited the National Hemophilia Foundation (NHF) national offices in New York City in...
Dave Meuleman, a materials engineer in his 50s from Canton, Michigan, stepped outside his comfort zone when he sat down...
In each issue of HemAware , we take a look at how local NHF chapters and associations are making a...
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