Haemophilia Foundation Australia (HFA) represents people with haemophilia, von Willebrand disorder and other related inherited bleeding disorders, and their families through: Advocacy and Representation,Education and Research.

HFA works with a network of State and Territory Foundations to ensure everyone with bleeding disorders in Australia has access to the worlds best practice treatment and care.  HFA is a National Member Organisation of the World Federation of Hemophilia, and participates in activities to improve access to treatment and care to people with bleeding disorders around the world.