HFA News & Notes

HFA Observes National Hepatitis Awareness Month

HFA Observes National Hepatitis Awareness Month FOR IMMEDIATE RELEASE: May 3, 2012 Contact: Richard Pezzillo [...] Read More >>

Community Pharmacists Lose Bid to Immediately Block Express Scripts-Medco Deal

By Rebecca Adams, CQ HealthBeat Associate Editor A federal judge has denied the request of a group of community [...] Read More >>

People with Bleeding Disorders and HCV

Link to Access HCV Therapy Site Friends and supporters, We should all be enormously encouraged by the increasing [...] Read More >>

Contact Info

Hemophilia Federation of America
210 7th St. SE, Suite 200B
Washington D.C., 20003
800.230.9797
202.675.6984
202.675.6983

© 2011 Hemophilia Federation of America · Board of Directors Only · BB Admin Only · Privacy & Legal

What We Do

Hemophilia, vonWillebrand and other Bleeding Disorders are lifelong conditions that require ongoing care and support. To provide support to this community, HFA provides programs, services, meetings, outreach and advocacy education.

Programs: HFA provides a variety of educational, wellness and financial resources to help the bleeding disorders community stay healthy, and informed. We foster meaningful connections and support through good times and times of hardship. Check out HFA’s Programs today!

Meetings / Events: Every year HFA hosts a national Symposium for people with bleeding disorders and their families. This meeting rotates around the country, bringing the family community together nationally. An estimated 700 attendees participate in rap sessions, networking and receive education from top national speakers and educators. Attend Symposium!

 


Advocacy: If you are new to hemophilia and bleeding disorders or have years of experience championing this community, we welcome you! Join our Outreach and Advocacy Education efforts!

Working together and supporting each other, we can make a difference for people with Bleeding Disorders such as vonWillebrand and hemophilia!