Advocacy

Advocacy

HemAware has everything you need to know about inheritable blood and bleeding disorders. Read now to learn more.

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...
When Val D. Bias became chief executive officer of the National Hemophilia Foundation (NHF) in 2008, he wasn’t just the...
As a board member of Hemophilia of South Carolina, Renita Johnson knows that better care for people with bleeding disorders...
A report from the bleeding disorders policy front lines.
Advocate Jennifer Banks and her family's experience at NHF 2019 Washington Days.
The bleeding disorders community needs everyone to get involved.
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Contact HANDI, NHF's resource center for additional information on bleeding disorders.