The Children’s Tumour Foundation (CTF) is the only dedicated support service for families impacted by Neurofibromatosis (NF) in Australia.
Our mission is to provide hope for everyone impacted by Neurofibromatosis in Australia by advocating for change, advancing research and empowering this community with the knowledge, connections and support at every stage of their journey.
Conquering NF is about more than just finding a cure. 
FIND OUT MORE
ADVOCACY--- SUPPORT--- RESEARCH
READ OUR 2021-2023 STRATEGIC PLAN
WHO WE SUPPORT
Our community includes everyone living with Neurofibromatosis (NF) in Australia (diagnosed and/or undiagnosed), along with their family, carers and friends. It also includes healthcare professionals, employers and educators.
NF can affect anyone regardless of age, ethnicity, gender or family history.