Haemophilia Foundation Australia (HFA) represents people with haemophilia, von Willebrand disorder and other related inherited bleeding disorders, and their families through advocacy and representation, education;and research. Services include bleeding disorder information, treatment centre contacts, support for people living with medically acquired Hepatitis C or HIV/AIDS including pre and post test counselling. See website links for further information: EntryProcedures 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 for haemophilia, von Willebrand Disorder and related bleeding disorders, hepatitis C and HIV.