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.

Meet a few of the dedicated state-based advocates building strong partnerships to protect and improve the lives of people with...
On March 7–9, 2018, hundreds of people from around the country converged on Washington, DC, for the National Hemophilia Foundation’s...
On March 9, more than 500 people with bleeding disorders and their families put on their red ties and prepared...
Clinical trials provide important information about how well drugs and devices work and how safe they are, but they’re not...
Against a backdrop of a possible repeal of the Affordable Care Act (ACA), the National Hemophilia Foundation’s (NHF) Washington Days...
The minimum amount of clotting factor a country requires to avert death in life-threatening instances is 1 international unit (IU)...
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...
Chat Icon
Need Info? Ask NHF!
Contact HANDI, NHF's resource center for additional information on bleeding disorders.