Community in Action

Nationwide, the inheritable blood and bleeding disorders community is taking action to raise awareness for the cause. Read more to get involved and get inspired!

You can turn to social media for information on virtually anything, from the private lives of movie stars to makeup...
When Patrick James Lynch launched BloodStream in 2016, he sought to create something that didn’t yet exist: a podcast featuring...
At every life stage, a blood or bleeding disorder can lead to new questions and concerns. The Steps for Living...
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...
Ronia Cole, 52, of Redford Township, Michigan, has lived with a bleeding disorder since she was a toddler. “I’d take...
Ask a Social Worker is a monthly column featuring questions from the community and answers from members of NHF’s Social...
Having a rare disease like hemophilia means you don’t often get to see people who share your disease portrayed in...
For organizations such as the National Hemophilia Foundation (NHF), fundraising is a way to raise awareness and much-needed funds for...
Orlando Vives has a severe form of hemophilia B and has been able to lead a relatively normal life, thanks...
Racial and ethnic disparities in healthcare are nothing new. Black and Latinx people have long struggled with getting others to...
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