Who We Are

Haemophilia Foundation Australia (HFA) is the national peak body that represents people with haemophilia, von Willebrand disorder and other inherited bleeding disorders, and their families through:

  • Representation and Advocacy 
  • Education
  • Research

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.