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.