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

Priorities

 

Our intent as a grassroots organization is to provide the information and tools needed for individuals with bleeding disorders and their families to participate in monitoring, advocating, and supporting federal and state public policies that impact the lives of people with bleeding disorders.

 

Access

Goal: Affordable access to providers, treatments and products for the most efficient and effective treatment of bleeding disorders.

» FEDERAL  ISSUES

» STATE ISSUES


Safe Therapies

Goal: Access to accurate information and a voice in holding manufacturers and the federal government accountable for providing safe therapies. (Learn more)>


Data Collection

Goal: Data must provide the foundation for improved and accurate public understanding of bleeding disorders, decision-making by providers and payers, and improved care for patients. This process must include individuals with bleeding disorders and thier families. (Learn more)>


Patient Protection and Affordable Care Act (PPACA)

Goal: Implementation of the PPACA should provide every American, especially individuals with a bleeding disorder access to a health care system that is high-quality, affordable and comprehensive. (Learn More)>