Connecting the NF community with information, services and each other is a huge part of what we do.
Our NF community events are designed to empower and educate you; helping you to build stronger connections between both adults, children living with the condition, as well as their families.
NF VIRTUAL EVENTS
Due to restrictions around events and gatherings as a result of the COVID-19 pandemic, we have introduced several online support initiatives to bring members of our community together during an uncertain time.
CTF Webinar Series
The children's Tumour Foundation is proud to play host to an Australian based neurofibromatosis webinar series.LEARN MORE
covid-19: an update on our events
Due to the increasing spread of COVID-19 and the Government restrictions on social gatherings, we regret that many of our events have been cancelled or postponed for the foreseeable future.
We are reviewing events we run on a case-by-case basis, taking into consideration not only the needs of NF patients and their families, but also our own staff, other potential event attendees and the broader community’s health.
As the situation changes and we can commence planning for future events, we will keep you updated on this page, and via email and social media.
If you’re feeling anxious or worried, we want to hear from you. We may not be able to bring you all together right now, but we can still provide you with resources, connections or maybe just a shoulder to cry on (or to share a laugh with).
We know that staying connected is a good way to cope.