Community in Action

Black Women with Bleeding Disorders Are Striving to Be Seen and Heard

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...

COVID-19 has disrupted the lives of everyone, including young adults, who have had to navigate classes and commencements, weddings and...

The end-of-the-year giving season is an ideal time to donate to the National Hemophilia Foundation (NHF) and support its research...

In the summer of 2019, while training for the New York City marathon, Nicole Kaes of Brooklyn, New York, woke...