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  • Fio's Story

    Fio's Story

    When baby Fio came home from a family holiday with a cough and a little tiredness, her parents never imagined it would mark the beginning of a life-changing journey. Within days of their return, their bubbly little girl was diagnosed with stage 4 neuroblastoma. Fio’s mum, Em, shares their story. Read more

  • Emily's Story

    Emily's Story

    When 19-month-old Emily went to the GP for what seemed like a simple cold, her parents never imagined it would change their lives. Emily's mum, Jade, shares their story. Read more

  • Donate today

    Donate today

    One in two children with aggressive neuroblastoma will not survive. Neuroblastoma is the number one toddler cancer. We need your help to find effective treatments. Donate today to support world class Australian research into developing less toxic, more effective treatments, with the ultimate goal of finding a cure. Donate as an individual or business and receive a tax-deductible receipt for all donations over $2. Read more

    Target $500,000 Raised so far $293,220
    Please select a donation amount (required)
    Donate now Fundraise Read more
  • Grace's Story

    Grace's Story

    Little Grace was just 8 months old when her mum, Brooke, noticed a concerning change—Grace’s leg strength and movement seemed to be decreasing. After a hospital visit and an MRI, Brooke and her husband received devastating news: a cancer-like mass had been found in Grace’s chest. Read more

  • Fio's Story
  • Emily's Story
  • Donate today
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family stories

Elsie's Story

Elsie's Story

Little Elsie was only six-months-old when her parents, Phil and Jayde, rushed her to hospital, concerned that what seemed like a viral infection might be something more serious. Tests revealed the devastating truth: Elsie had a cancerous tumour in her abdomen. Elsie’s dad, Phil, shares their story. Read more

Published: 10th February, 2026

Updated: 23rd February, 2026

Caitlyn's Story

Caitlyn's Story

At 16 years old, Caitlyn’s life changed in ways no teenager, and no family, could ever imagine. What began as a simple pain in her side quickly unfolded into a devastating diagnosis of neuroblastoma. Caitlyn’s mum, Tanya, shares their story. Read more

Published: 5th January, 2026

Updated: 25th February, 2026

Fio's Story

Fio's Story

When baby Fio came home from a family holiday with a cough and a little tiredness, her parents never imagined it would mark the beginning of a life-changing journey. Within days of their return, their bubbly little girl was diagnosed with stage 4 neuroblastoma. Fio’s mum, Em, shares their story. Read more

Published: 5th January, 2026

Updated: 10th February, 2026

Emily's Story

Emily's Story

When 19-month-old Emily went to the GP for what seemed like a simple cold, her parents never imagined it would change their lives. Emily's mum, Jade, shares their story. Read more

Published: 21st October, 2025

Updated: 26th November, 2025

Donate today

Donate today

One in two children with aggressive neuroblastoma will not survive. Neuroblastoma is the number one toddler cancer. We need your help to find effective treatments. Donate today to support world class Australian research into developing less toxic, more effective treatments, with the ultimate goal of finding a cure. Donate as an individual or business and receive a tax-deductible receipt for all donations over $2. Read more

Published: 25th July, 2025

Updated: 23rd September, 2025

Author:

Grace's Story

Grace's Story

Little Grace was just 8 months old when her mum, Brooke, noticed a concerning change—Grace’s leg strength and movement seemed to be decreasing. After a hospital visit and an MRI, Brooke and her husband received devastating news: a cancer-like mass had been found in Grace’s chest. Read more

Published: 24th June, 2025

Updated: 13th April, 2026

Nevaeh's Story

Nevaeh's Story

The arrival of Bec’s much longed for daughter, Nevaeh, was tinged with sadness. Her birth coincided with the heartbreaking loss of Bec’s father, David, who passed away on the very same day. Bec had little time to process the whirlwind of emotions, as just weeks later, Nevaeh was diagnosed with neuroblastoma. Bec shares their story. Read more

Published: 24th June, 2025

Updated: 9th June, 2026

Hamish's Story

Hamish's Story

Doctors initially thought 11-year-old Hamish’s leg pain was normal teenage growing pains. However, after the pain became debilitating, Hamish’s parents took him to hospital where they received the devastating news that Hamish had stage 4 neuroblastoma. Read more

Published: 4th June, 2025

Updated: 4th July, 2025

Frances' Story

Frances' Story

On Father’s Day in 2021, a young family’s world was turned upside down. At just 10 months old their son, Frances, was diagnosed with stage 4 neuroblastoma with the MYCN amplification—an aggressive, high-risk form of cancer. Read more

Published: 4th June, 2025

Updated: 13th April, 2026

Chloe's Story

Chloe's Story

On Thursday, September 20, 2024, the lives of little Chloe and her family changed dramatically.  It was the first day they ever heard the word “neuroblastoma”.  Within 24 hours they went from being on a family holiday to being admitted to the oncology ward in Queensland Children’s Hospital. Read more

Published: 24th April, 2025

Updated: 22nd April, 2026

Luna's Story

Luna's Story

In July 2023, Luna’s parents heard six little words no parent ever wants to hear, “I’m sorry, your child has cancer.” It was discovered that Luna had high-risk stage IV neuroblastoma, a rare, aggressive, and fast spreading childhood cancer. Read more

Published: 25th February, 2025

Updated: 25th February, 2026

Kara's Story

Kara's Story

Thirty years have passed since Susan and Peter Le Rossignol lost their beautiful daughter, Kara to neuroblastoma. Here they share their story and although over three decades have passed, many will recognise elements of this story and it highlights the need to do more. Read more

Published: 19th February, 2025

Updated: 17th March, 2025

Hazzy's Story

Hazzy's Story

Tyler and Alix, parents to one-year old Harris (or Hazzy), were living fulfilling lives in Hobart.  When they took their baby, who had been unsettled for a few weeks, to the hospital, they never imagined their world was about to be turned upside down. Read more

Published: 10th February, 2025

Updated: 25th February, 2026

Raphael's Story

Raphael's Story

Although Raphael was a bright and active baby, persistent breathing issues worried his mum, Kristen. Despite investigation, nothing untoward could be found. Raphael was nearly two years old when another serious breathing episode occurred which led to a shock diagnosis of stage 2 neuroblastoma. Kristen shares their story. Read more

Published: 1st February, 2025

Updated: 7th May, 2025

Rosalie's Story - A Parent's Perspective

Rosalie was a busy mum co-running the family business when her youngest child, Jullian, developed symptoms similar to a common cold. While seemingly benign, Rosalie couldn’t shake the feeling that something wasn’t right. She shares her story of how her toddler was eventually diagnosed with Stage 4 neuroblastoma. Read more

Published: 14th January, 2025

Jullian's Story

Jullian's Story

19-year-old Jullian shares his story of being diagnosed with neuroblastoma as a toddler, the lasting impact the disease has had on his life, and how it's inspired him to help children in the future. Read more

Published: 9th January, 2025

Updated: 19th May, 2026

Patrick's Story

Patrick's Story

Patrick was born a healthy baby in August 2020, but at just eight weeks old, his parents, Kimberley Rowlings and Shane Zahra, began to notice something wasn't quite right. Read more

Published: 30th October, 2024

Updated: 13th October, 2025

Oli's Story

Oli's Story

After developing a limp and suffering a broken femur, Oli's parents took him to hospital. Tests revealed that at just two years of age, little Oli had neuroblastoma throughout his tiny body. After extensive treatment over a number of years and in Australia and US, Oli is now cancer-free. Read more

Published: 12th August, 2024

Updated: 28th February, 2025

Jackson's Story

Jackson's Story

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

Published: 13th March, 2024

Updated: 14th January, 2026

Mackenzie's Story

Mackenzie's Story

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

Published: 13th March, 2024

Updated: 28th February, 2025

Zach's Story

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. 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

Published: 20th February, 2024

Updated: 7th May, 2025

Author: Lynette Haines

Evie's Story

Evie's Story

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

Published: 11th February, 2024

Updated: 3rd June, 2024

Author: Lynette Haines

Harry's Story

Harry's Story

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

Published: 8th November, 2023

Updated: 31st January, 2026

Henry's Story

Henry's Story

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

Published: 26th October, 2023

Updated: 28th February, 2025

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Latest

  • August 2026

    August 2026

    On Sunday 9 August 2026, take on Australia's most iconic fun run and help make a difference for children with neuroblastoma. Starting in Sydney's CBD at Hyde Park and finishing at Bondi Beach, City2Surf is a 14km event that brings together thousands of runners, walkers and fundraisers each year.

  • National Childhood Cancer Roadmap Recognises CAR T-Cell Therapy as a National Priority

    National Childhood Cancer Roadmap Recognises CAR T-Cell Therapy as a National Priority

    Neuroblastoma Australia has welcomed the release of the National Childhood, Adolescent and Young Adult Cancer Roadmap, describing it as an important step forward for children and families affected by cancer.

  • Neuroblastoma Australia Responds to Federal Budget Announcement

    Neuroblastoma Australia Responds to Federal Budget Announcement

    Neuroblastoma Australia is extremely disappointed the Federal Budget did not include specific funding for CAR-T Cell treatment for solid tumours - it’s a devastating omission for Australian children diagnosed with neuroblastoma.

  • Oaten's | Raising funds for research into neuroblastoma

    Oaten's | Raising funds for research into neuroblastoma

    I'm fundraising for Neuroblastoma Australia, to raise funds for vital research into better, kinder and more effective treatments for the children's cancer neuroblastoma. Please show your support by donating via this page.

Most read

  • What is neuroblastoma?

  • Donate today

    Donate today

    One in two children with aggressive neuroblastoma will not survive. Neuroblastoma is the number one toddler cancer. We need your help to find effective treatments. Donate today to support world class Australian research into developing less toxic, more effective treatments, with the ultimate goal of finding a cure. Donate as an individual or business and receive a tax-deductible receipt for all donations over $2.

  • Detection, diagnosis & staging

    Detection, diagnosis & staging

    Know about symptoms of neuroblastoma, detection, diagnosis and different stages of neuroblastoma childhood cancer.

  • How common is neuroblastoma?

  • How dangerous is neuroblastoma?

  • Our Story

    Our Story

    Neuroblastoma takes the lives of more children under five than any other cancer. Help us fund new research to find a cure within our lifetime and save toddlers' lives.

  • How is it diagnosed?

  • Why does this cancer form?

  • Golf2Cure 2025

    Golf2Cure 2025

    Our 2025 charity golf day, Golf2Cure, will take place on Thursday, June 26 at the prestigious Lakes Golf Club at Eastlakes, Sydney. The aim of the day is to have fun, increase awareness of neuroblastoma, and to raise funds for research into this devastating childhood cancer so we can find treatments that are more effective and less toxic. 

  • Key Statistics

    Key Statistics

    Know key statistics about the childhood cancer, neuroblastoma. Neuroblastoma is the most common solid tumour of childhood and its treatment. Most neuroblastomas, made up of cells found in nerve tissues of the body, start in the adrenal glands.

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