What We Do

The primary aim of the Foundation is to support people with haemophilia and associated bleeding disorders and their families, and those affected by blood borne viruses as a result of the use of blood products necessary for treatment.

HFV endeavours to:

  • Develop awareness of HFV and the programs and services available, among people with bleeding disorders and the wider community
  • Develop and maintain relevant support programs, information and activities for members
  • Provide support, both emotional and financial
  • Respond and act on behalf of people with bleeding disorders
  • Liaise with and educate the community on haemophilia and blood borne viruses
  • Maintain good working relationships with both treating hospitals and their staff


HFV is committed to child safety. Our child safety statement is available for review below.

HFV Child Safety Statement