Children's Tumour Foundation of Australia

ABOUT US
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).they 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.
vision:
A life without limitations for everyone living with Neurofibromatosis.

Mission:
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 needed at every stage of their journey.

OUR VALUES:
• they are the link that connects people with NF to services. they are dedicated to raising money to fund vital research, awareness and practical support for people with all types of NF.
• they are focused. they work in pursuit of an important mission and understand that many people are counting on us.
• they are a united and collaborative team. Teamwork comes naturally to us because of their passion and dedication to do the absolute best they can to support everyone impacted by NF.
• they are not afraid to work hard and know that trust must be earned. they accept responsibility for their actions, hold ourselves accountable for their results, and take ownership of their mistakes.
• they are continually evolving. they encourage feedback and are always striving to do things better.they are confident enough to know that just because they do things a certain way now, doesn’t mean they can’t find a better way.