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.

When Dawn Rotellini started the Rocky Mountain Hemophilia and Bleeding Disorders Association in Bozeman, Montana, 15 years ago to serve...
The National Hemophilia Foundation (NHF) is proud to announce the debut of our advocacy website in conjunction with our annual...
Alex Borstein is notable for a number of things—as the voice of the preternaturally patient Lois Griffin on FOX’s long-running...
California is the place you want to be this year, as the National Hemophilia Foundation (NHF) hosts its 65th Annual...
With the Hudson River glimmering in the background, the National Hemophilia Foundation (NHF) welcomed more than 230 people to its...
The National Hemophilia Foundation (NHF) is excited to welcome the bleeding disorders community to its 65th Annual Meeting October 3–5...
A horde of fit athletes will gather ­September 7–8 on the banks of ­Canandaigua Lake in upstate New York to...
California, here we come! NHF’s 65th Annual Meeting will take place in sunny Anaheim, California, on October 3–5, offering three...
Every year on April 17, the global bleeding disorders community comes together to mark World Hemophilia Day (WHD). World Hemophilia...
The National Hemophilia Foundation (NHF) provides training for its chapters and other community members to support its programs. As part...
HemAware will soon be available in a new format—in an iPad app. Starting in fall 2013, you will be able...
Telling stories, especially personal ones, can be a powerful way to change the way people think. The National Hemophilia Foundation...
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Need Info? Ask NHF!
Contact HANDI, NHF's resource center for additional information on bleeding disorders.