Our people

We HELP everyone impacted by nf NAVIGATE A PATHWAY FROM FEAR TO HOPE

Formally known as the Neurofibromatosis Association of Australia (NFAA), the Children’s Tumour Foundation was established in 2010 and has grown from a volunteer-based support service to become the peak body in Australia for those impacted by Neurofibromatosis (NF).

We provide hope for everyone impacted Neurofibromatosis in Australia by advocating for change, advancing research and empowering this community with knowledge, connections and support at every stage of their journey. 

Our Staff

The Children's Tumour Foundation is staffed by a small but mighty team committed to our mission and exceeding our community and partners’ expectations.

Our Board

We are governed by an active and experienced Board who work with our management team to ensure we are accountable to all stakeholders.  

Our Ambassadors

Meet our Ambassadors! From members of the NF community to high profile Aussies and Legacy supporters, many voices champion NF.

Medical Advisory Panel

The Medical Advisory Panel to provide professional guidance and advice on the medical and scientific aspects of the information services provided by CTF as well as any research grants made by CTF.

Community Advisory Panel

The Community Advisory Panel provide guidance and advice on the services provided by the CTF to all individuals and families impacted by Neurofibromatosis (NF).