Search Stories | HemAware

Forward March

Despite seeking treatment for her symptoms for years, Jill R. Birdwhistell, PhD, was never diagnosed with a bleeding disorder. Heavy...

In each issue of HemAware , we “Take 5” with people in the bleeding disorders community and spotlight their efforts...

My Journey

HemAware “ Takes 5” with people in the bleeding disorders community and spotlights their efforts with just five questions. Here...

My Journey

At the National Hemophilia Foundation’s (NHF’s) 62nd Annual Meeting in New Orleans in November 2010, the National Youth Leadership Institute...

The National Hemophilia Foundation’s (NHF’s) Annual Meeting in November 2010 was our first NHF meeting. We were all excited to...

Von Willebrand Disease, Community in Action

I anticipated my first National Hemophilia Foundation (NHF) Annual Meeting with a lot of excitement, but without many expectations. My...

Although few people relish public speaking, hitting a lifetime benefits cap or being denied access to insurance because of a...

Advocacy

Parents of children with hemophilia and other bleeding disorders are very familiar with the routines and challenges that come with...

Hemophilia A&B, Von Willebrand Disease, Family Matters

HemAware “ Takes 5” with people in the bleeding disorders community and spotlights their efforts with just five questions. Here...

My Journey

When Ramiro Gomez was a freshman in high school, he was already starting on the varsity soccer squad in his...

Pain Management

HemAware “ Takes 5” with people in the bleeding disorders community and spotlights their efforts with just five questions. Here...

My Journey

National Hemophilia Foundation CEO Val D. Bias and New York City nightlife photographer Patrick McMullan called attention to women’s bleeding...

Von Willebrand Disease, Community in Action, Women's Bleeding Disorders