Connecting the NF community with information, services and each other is a huge part of what we do.
The Children’s Tumour Foundation (CTF) is the only support service for families living with Neurofibromatosis (NF) in Australia. NF is a life-long genetic condition with few treatment options and no cure. The NF journey from diagnosis through to treatment is challenging and most of what people will experience is unknown.
The CTF exists to provide a pathway from fear to hope by investing in promising research, advocating for better resources and empowering individuals and their families with knowledge, connections and support needed at every stage of their journey.
Because for us, conquering NF is about more than just finding a cure.