Shortly before his first birthday, Jackon's family noticed he had developed a limp in his right leg. Further tests revealed Jackson had neuroblastoma. His dad, Andrew, shares their story. Read more
Mackenzie was just two weeks old when her parents noticed her abdomen was large and firm to touch. After an emergency referral to the Queensland Children's Hospital, Mackenzie was diagnosed with neuroblastoma. Mackzenie's mum, Ally, shares their story. Read more
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. Four years later and Zach in remission, back at school, and in February 2024 was given the final all clear to ring the bell! Read more
Logan was a healthy baby, eating well and enjoying day-care. However, at 11 months Logan was struggling to recover from frequent infections. At this time, his parents Alyssa and Shane noticed Logan's tummy was unusually hard and round. They rushed Logan to hospital where he was diagnosed with neuroblastoma. Logan's dad, Shane, tells the family's story. Read more
In 2013, Joshua and Sarah Weir's two-year-old daughter, Evie, was diagnosed with stage 4 neuroblastoma. Sarah shares Evie's story and how this amazing little girl inspired Evie's Army. Read more
Just over a month before Harry’s 9th birthday, his parents were told the devastating news that Harry was diagnosed with High-Risk Neuroblastoma. Harry’s mum, Julia, tells us their story. Read more
After a fall at school resulted in a painful lump in his tummy, Henry was rushed to The Royal Children's Hospital where he was diagnosed with neuroblastoma. Henry's dad, George, shares their story below. Read more
After experiencing a limp and persistent fever that culminated in full body pain and night-sweats, three-year-old Ryder was eventually diagnosed with neuroblastoma. Ryder's parents, Katherine and Jarrad, share their story. Read more
On New Year’s Day 2022, and at just three years old, Sirin was tested for and diagnosed with stage 4 high risk neuroblastoma. Her mum, Wannee, tells her story. Read more
In 2018, 16-month-old Marko was diagnosed with neuroblastoma. Despite successful surgery to remove a large tumour, Marko later developed a persistent limp that required further investigation. Marko's family were devastated to find that the cancer had spread to numerous parts of his body. Marko's mum, Jelena, shares his story. Read more
Help us beat the number one toddler cancer. Please donate today to support world class Australian research into developing better, safer treatments with the ultimate goal of finding a definitive cure for all children diagnosed with neuroblastoma. Currently one in two children with aggressive neuroblastoma will not survive and we need your help to support the development of effective treatments. Donate as an individual or as business and receive a tax-deductible receipt for all donations over $ Read more
Although she experienced some milestone delays, 8-month-old Hayley was seemingly a healthy baby. However, after she developed an unusual rash and foot spasms, Hayley was taken to hospital where she was diagnosed with neuroblastoma. Read more
Just a few months before her 2nd birthday, Fiapule was diagnosed with stage 4 neuroblastoma. Read more
Xavier was diagnosed with stage 4 high risk Neuroblastoma at the end of March 2021, when he was just 3.5 years old. Read more
In January 2021, Lucy was just like every other seemingly healthy 5.5-year-old-girl, excitedly preparing to start school, when she was diagnosed with neuroblastoma. Read more
At five days old, Elijah was diagnosed with neuroblastoma and just first week of his life, Elijah underwent two biopsy surgeries, many blood tests and scans. Read more
A normal, bubbly toddler, Willow Lawton was diagnosed with neuroblastoma at the age of 2 years and 9 months. Read the story of this brave little girl and her fight with neuroblastoma. Read more
Ethan's diagnosis was Stage 4 Neuroblastoma with a tumour on his adrenal gland, a secondary tumour on his lower spine and a disease in pretty much every bone of his body. Read more
At seven months, Kalynda lost complete movement in her body. Further diagnosis revealed a mass in her chest cavity pushing out her ribs and compressing her spine. It was an intermediate grade neuroblastoma. Read more
In January 2018 after being dismissed many times from Emergency with what was thought to be a 'virus', 18-month-old Eleanor was diagnosed with Stage Four High Risk Neuroblastoma and began the fight of her life. Read more
After months of misdiagnoses, including a middle-of-the-night emergency trip to the hospital, Emeline’s mum took her to a paediatric gastroenterologist believing her tummy issue was severe constipation. It turned out to be neuroblastoma. Read more
Our June Run2Cure 2021 Superhero, Theodore Hilton is a bubbly 2 year old and the youngest of 3 beautiful sons. On Saturday, September 4th 2021, he and his family will be supporting the Run2Cure 2021 to raise awareness and funds for Neuroblastoma childhood cancer. Read more
Emma and Sam welcomed beautiful baby Roy into their lives at the very height of the 2020 COVID-19 pandemic. The last thing this courageous family expected was a neuroblastoma cancer diagnosis. Read more
Our first Run2Cure 2021 Superhero, Noah Lord is a cheerful, spirited, strong-willed 3 year old, who has not let Neuroblastoma slow him down. On Saturday, September 4th 2021, he and his family will be supporting the Run2Cure 2021 to raise awareness and funds for Neuroblastoma childhood cancer. Read more