Rare Bleeding Disorders

Rare Bleeding Disorders

Read more about the D'Ambrosios in stepmom Cheryl's own words, in our Community Voices section. A hangnail hardly constitutes a...
Read more about this family's experience in the Factor V Deficiency article. Both my stepdaughters were born with severe factor...
Skye Peltier’s life changed on a playground when she was 5 years old. After going down a slide, she lingered...
When Emily Bartko, 4, of Las Vegas, was an infant, bruising came easily. All it took was the pressure from...
In January 2009, the US Food and Drug Administration (FDA) approved CSL Behring’s RiaSTAP™ for the treatment of acute bleeding...
Update, January 2014: On December 23, 2013, the FDA approved Tretten, Coagulation Factor XIII A-Subunit (Recombinant), which is the first...
Blame it on the Girl Scout cookie. That’s what Josh Beck, 27, of Franklin, Wisconsin, was eating when he was...
Lisa and Michael Louwers are both doctors, but the Farmington Hills, Michigan, couple didn’t know much about hemophilia or other...
When Murali Pazhayannur slipped while getting into a rickshaw during a Calcutta monsoon, he had no inkling he’d still be...
The National Hemophilia Foundation (NHF) has counterparts across the country advocating for the needs of patients with blood disorders ranging...
Throughout his life, Dan Bond has offered his time and body to the cause of science. The Galveston, Texas, engineer...
Chat Icon
Need Info? Ask NHF!
Contact HANDI, NHF's resource center for additional information on bleeding disorders.