Who We Are
Haemophilia Foundation Australia (HFA) is the national peak body that represents people with haemophilia, von Willebrand disease and other bleeding disorders, and their families.
Our vision - active, independent and fulfilling lives for people in our bleeding disorders community.
We aim to achieve this through our mission - inspiring excellence in treatment, care and support through representation, education and the promotion of 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.
Date last reviewed: 17 June 2020