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.

The National Hemophilia Foundation (NHF) is pleased to announce that it was awarded the bid to host the World Federation...
More than 300 members of the bleeding disorders community gathered in Washington, DC, on March 8 for NHF’s annual advocacy...
The US healthcare system is challenged by high costs during this tough economic period. Decisions about how to rein in...
The bleeding disorders community is in a unique period of drug development. Almost every pharmaceutical company currently producing factor products...
Read about the history of HTC funding and the growing needs. With the federal deficit now in the trillions, one...
Read about advocacy efforts for the hemophilia treatment center network.
By now, most people with hemophilia and other bleeding disorders and their families know the Patient Protection and Affordable Care...
Repealing the 2010 healthcare reform law is on the agenda of many of the Republican and Tea Party representatives who...
Although few people relish public speaking, hitting a lifetime benefits cap or being denied access to insurance because of a...
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.
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Contact HANDI, NBDF's resource center for additional information on bleeding disorders.