Help us reach our goal!

Join the Mega Hero March to conquer NF!

The NF Mega Hero March is a walk for the NF Community, family and friends to get involved to raise funds for research and awareness into NF.  

Walks are taking place in 6 cities around Australia including: Sydney, Melbourne, Brisbane, Adelaide, Port Macquarie & Canberra.  

The March, The Baton and The Cape!

Each city will have one Mega Hero Baton with the aim to have as many people possible, carrying it as they walk. Also as part of this special event, everyone that registers will get their VERY OWN YELLOW CAPE!

The baton and the cape demonstrate the Mega Hero powers of adults and children with NF and gives the power of freedom, courage and determination to help conquer NF.



8:30am: Arrive at location, check in and collect your mega hero cape!
9:00am: NF Mega Hero March kicks off in each city for walk
11:00am -11:30am: Return to enjoy something to eat and some family friendly activities at the event site.
1:00pm: Event Ends

What to bring

Remember you will need a hat, sunscreen and a water bottle to conquer the march! 

We suggest one person takes a back pack to hold everyone's belongings.


After the walk we will provide you with lunch and there will be food trucks available to purchase more food. Plus we will have some fun activities for the kids.

Want to walk a shorter distance?

Each city has the option to walk 2km if the longer walk is too far but if you intend to do this the cost to register still remains the same.


Children's Tumour Foundation of Australia

The Children’s Tumour Foundation of Australia (NF Australia) provides care and support to those impacted by Neurofibromatosis (NF), the umbrella term for three genetic conditions (NF1, NF2, Schwannomatosis) that cause tumours to grow on nerves throughout the body.

The most common form of NF is Neurofibromatosis Type 1 (NF1). Although usually diagnosed in children, NF is a lifelong medical condition and can affect many organs in the body, including the skin, eyes, bones, and nervous system.

The Foundation is dedicated to providing information and support, public awareness, and raising funds to develop effective treatments and find a cure for NF.

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