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 mission is to inspire excellence in treatment, care and support through representation, education and the promotion of research.
Our vision is for everyone in our bleeding disorders community to lead active, independent and fulfilling lives.
Our goals:
effective advocacy
strategic education and communication
financial sustainability
to advance research, care and treatment
best practice governance
to be the trusted national representative organisation and recognised community voice on bleeding disorders.
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.
Haemophilia Foundation Australia Inc is a registered charity with the Australian Charities and Not-for-profits Commission (ACNC).