Haemophilia Foundation Australia (HFA) represents people with haemophilia, von Willebrand disorder and other related bleeding disorders and their families. We are committed to improving treatment and care through representation and advocacy, education and the promotion of research. HFA supports a network of State and Territory Foundations in Australia.



As a National Member Organisation of the World Federation of Hemophilia, HFA participates in international efforts to improve access to care and treatment for people with bleeding disorders around the world.


  


Link to Red Run Classic 2008 page


 Link to HFA National Hepatitis C Needs Assessment Report. "A double whammy": living with a bleeding disorder and hepatitis C







(Website last updated 20/6//08)


News / Events

Mon, May 19 2008
World Hepatitis Day World Hepatitis Day

Thu, May 1 2008
HFA Research Grants - now available!

Mon, Apr 14 2008
World Haemophilia Day 2008 – Count me in! World Haemophilia Day 2008 – Count me in!

Tue, Dec 18 2007
Damon Courtenay Memorial Endowment Fund

Tue, Dec 18 2007
Vision and Leadership Awards Vision and Leadership Awards

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