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!

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...
The COVID-19 pandemic has affected the lives of all Americans in ways large and small. More than 600,000 Americans have...
Welcome to Ask a Social Worker, a new monthly column featuring questions from the community and answers from members of...
Summer camp is a time of freedom, exploration and fun. But for families who have children with bleeding disorders such...
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Contact HANDI, NHF's resource center for additional information on bleeding disorders.