www.facebook.com/NationalHemophiliaFoundation twitter.com/NHF_hemophilia /stories/feed

Hemophilia A&B

By Guy Young, MD | 04.17.2016

Three goals for the blood disorders community.

By Sarah M. Aldridge, MS | 07.30.2015

NHF provides awards and other fellowships to support research.

By Grant Hiura, NHF Education Coordinator | 04.28.2015

2014 gene therapy workshop.


My Life, Our Future aims to reach 5,000 participants in 2015.

By Beth Marshall | 11.17.2014

Inhibitor Education Summits provide hope.

By Matt McMillen | 11.17.2014

Shaping up without leaving home.

By Sarah Aldridge, MS | 11.15.2014

Teen’s AIDS advocacy endures 30 years after his diagnosis.


More than 1,100 patients from 17 HTCs participated.

By Sarah Aldridge, MS | 09.01.2014

New factor IX product may stretch time between infusions.

By Kadesha Thomas Smith | 01.30.2014

Understanding their connection to bleeding disorders.


Program launches newly redesigned website.

By Sarah Aldridge | 09.19.2013

Hemophilia gene therapy trials start delivering the goods.

By Kadesha Thomas Smith | 09.19.2013

NHF spokesperson Alex Borstein found success, levity in comedy.

By Emily Wojcik | 08.28.2013

A Q&A with NIH’s W. Keith Hoots, MD.

By Sarah Aldridge | 07.11.2013

Added diagnoses of HIV, hepatitis C can also cause bone loss.

By Heather Boerner | 07.11.2013

Joining forces in the bleeding disorders community.

By Michael Recht, MD, PhD | 07.10.2013

It’s an exciting time for bleeding disorders community.


Pilot sites approved and first patients enrolled.


My Life, Our Future aims to unlock hemophilia.

By Val D. Bias | 04.10.2013

Benefits of genotyping are both individual and communal.