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.

For many years, Rodney Dalrymple, of Booneville, Mississippi, has managed his severe hemophilia A with a factor product that he...
Teddy Taylor’s parents were both top-tier college athletes, so organizing a sporting event to benefit the National Bleeding Disorders Foundation...
Joey Smiles: A Perfect Match When Joey Smiles, 44, was growing up in the 1980s and ’90s, treatment for hemophilia...
Nick McRae-Cyr knew he wouldn’t be going into construction like the rest of his family. Instead of a high-impact occupation...
The National Hemophilia Foundation (NHF) celebrates its 75th anniversary in 2023. Throughout the year, HemAware.org will be commemorating this special...
Ask a Social Worker is a monthly column featuring questions from the community and answers from members of NHF’s Social...
Ask a Social Worker is a monthly column featuring questions from the community and answers from members of NHF’s Social...
Nickie Fernandez remembers the first time he and his family met with their state senator in Salem, Oregon, in 2015...
NHF is keeping the bleeding disorders community informed.
For years, doctors dismissed Lisa Webb’s heavy bleeding as just something that women in her family had to endure. Despite...
While in-person fundraising events and other opportunities to gather face to face to aid the bleeding disorders community are largely...
On February 26-28, bleeding disorders advocates from around the country will convene in Washington, DC, for the National Hemophilia Foundation’s...
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Need Info? Ask NBDF!
Contact HANDI, NBDF's resource center for additional information on bleeding disorders.