Fighting For You

Fighting for You

Since the beginning of the coronavirus pandemic, the National Hemophilia Foundation (NHF) has sought to provide the bleeding disorders community...
For years, doctors dismissed Lisa Webb’s heavy bleeding as just something that women in her family had to endure. Despite...
When you’re getting ready to go to college, the checklist of what you’ll need is long: computer, backpack, a proper...
Picking the right health insurance plan and navigating the issues that arise can be difficult, time-consuming and oftentimes frustrating processes—especially...
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.
Washington Days attendees share their wisdom.
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Contact HANDI, NHF's resource center for additional information on bleeding disorders.