To ensure treatment and support for all people with bleeding disorders around.

Haemophilia Foundation Australia (HFA) represents people with haemophilia, von Willebrand disorder and other related inherited bleeding disorders, and their families. HFA works with a network of State and Territory Foundations to ensure everyone with bleeding disorders in Australia has access to the world’s 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.

Advocacy and Representation
Education
Research