Contact us

The Neuroblastoma Australia office is on Level 1, 441 Pacific Highway, Crows Nest NSW 2065.

The best way to contact us is through our email: [email protected]

If the matter is urgent please contact 0406 991 606.

Neuroblastoma Australia Incorporated is a registered charity with GDR Status and our ABN is 74 173 375 414.

In the news

All media queries to be directed to Jane Owen Public Relations via email: [email protected] or mobile: 0407 936 005.

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Donate today

Help us beat the number one toddler cancer. Currently, only 50% of those children diagnosed with aggressive neuroblastoma will survive five years after diagnosis – and a third of those children that do survive, will have long term side effects from their treatments. Please donate today to support world class Australian research into developing beter, safer treatments.

Latest

Maddie's Story #43km

This little gladiator makes the most of every moment, stopping to smell the roses, talk to a stranger, splash in muddy puddles.
Kahlilla's Story #14km

Little Lilla's light continues to shine. Always and forever.
Evie's Story

Six year old Evie lived and loved so fiercely. She will be forever missed.
Evie's Story #6km

Six year old Evie lived and loved so fiercely. She will be forever missed.

Jane Owen

Jane has worked in many PR roles for organisations and agencies in Australia, the UK and Hong Kong after completing a BA Comms from Charles Sturt University.
Michele Smith

After finishing her HSC , Michele did a three year Management Cadetship with Grace Bros/Myer in conjunction with completing an Advanced Management Certificate at Tafe. Michele has had numerous management roles with Myer and David Jones for thirteen years.
Jody Mullen

Jody’s professional background was in marketing and customer training and education, primarily in the software industry. As an active mother of two boys (10 & 13), she took time off when they were small, trained to become a running coach and has enjoyed coaching runners for the past several years.
Lynette Haines

Lynette is a versatile communications professional with a passion for making a difference. She holds a BA in Communications from the University of Technology and has over ten years of experience in providing communications, marketing and events services to both corporate and not-for-profit businesses.
Lucy Jones

Lucy is focused on driving change neuroblastoma survival rates through more research, having tragically lost her daughter Sienna to this cancer in 2010. When Sienna was first diagnosed, Lucy started fundraising with a small group of friends. The group 'Sienna Hoffmann and friends' raised over $725 000 for the Children’s Cancer Institute.

Run2Cure 2020

Start the new year with a Super Earlybird ticket and save 25% ! Join us at he #funrun4everyone which will take over The Domain, Sydney on Sunday, 31 May 2020!
Accessibility

Neuroblastoma Australia is committed to providing a website that is accessible to the widest possible audience, regardless of technology or ability. Our website endeavours to conform to level Double-A of the World Wide Web Consortium W3C Web Content Accessibility Guidelines 2.0.
Daily Mile Magic

My friends Paolo and Diana Carniel are parents to their beautiful boy Zach who is battling Neuroblastoma and Opsoclonus Myoclonus Syndrome. I'd like to help them raise funds for research to beating this childhood cancer.
Kahlilla's Story #14km

Little Lilla's light continues to shine. Always and forever.
Detection, diagnosis & staging

Most symptoms of neuroblastoma are caused by the growth of the cancer into nearby tissues or organs, or its spread to distant parts of the body such as bones or bone marrow.
What is neuroblastoma?

Neuroblastomas are cancers that start in early nerve cells (called neuroblasts) of the sympathetic nervous system. This means that tumours can be found anywhere along this system; most commonly (about 50%) start in the adrenal glands (above the kidney), or near the spine, chest, neck or pelvis.
Childhood Cancer Awareness Month

This September, wear gold and join our #hope campaign to raise awareness of all forms of children's cancer and the toll it takes on the youngest members of our community and their families.
Two research grants awarded to the Children's Cancer Institute

Today we announced funding grants to two ground breaking research projects which we hope will take us a step close to finding a cure for the rare and deadly children’s cancer neuroblastoma.
Zach's Story

Paolo and Diana Carniel had never heard of neuroblastoma before August 2018 when their son Zach, just five years old at the time, was first diagnosed.
Nixon's Story

Meet the sunny three year old who has endured more medical procedures than most people deal with in a lifetime.