Sarah’s Story
Robert’s daughter, Sarah, was diagnosed with Stage 4 neuroblastoma in December 1999 when she was seven years old - and sadly passed away a few years later at the age of 11. Nearly 20 years on since his loss, Robert remembers Sarah and shares her story here…
Violet’s Story - Childhood Cancer Awareness Month
At age 9 Violet told her mum that she had a monster in her tummy, prompting her mum Laura to seek medical support. After an ultrasound it was discovered Violet had neuroblastoma. Now having reached NEAD (no evidence of active disease) Laura reflects on the last year and the fears she still carries for her daughter’s health.
Max’s Story - Childhood Cancer Awareness Month
Max started chemotherapy on his 2nd birthday, after suffering with ‘dancing eye syndrome’ as a result of a neuroblastoma. Now turning 3 he has finished treatment and is awaiting results - having also raised over £10,000 for Neuroblastoma UK.
Tilly’s Story - Child Cancer Awareness Month
Tilly was diagnosed with Stage 4 Neuroblastoma in November 2021 and sadly passed away in September 2022 at the age of four. Tilly’s dad, Jonathan, shares her story here…
Cara's story - Childhood Cancer Awareness Month
After experiencing a lack of appetite, temperatures, lethargy, sickness and numerous trips to the GP, Cara was diagnosed with neuroblastoma.
Despite 19 months of treatment, Cara relapsed three months after completing front-line treatment. She was just three years old when she passed away in February 2020.
Rory's story
Rory was diagnosed with stage 4s neuroblastoma when she was just two weeks old and was given a 30% chance of survival. She not only had to fight cancer, but sepsis too. In May 2024 Rory rang the bell and has officially been declared cancer free, ready to start school this August.
Charlotte’s Story: From Neuroblastoma to the Paris Paralympics
25-year-old Charlotte was diagnosed with stage 4 neuroblastoma when she was just 12 weeks old. This summer, she will be representing Team GB, playing basketball in the Paralympic Games in Paris. Charlotte shares her story here…
Niamh's story
Niamh, now 25 years old, was diagnosed with neuroblastoma when she was 15.
In 2020, her cancer returned and she is once more undergoing treatment. She’s currently on a research drug trial but is doing well. This is her story.
Georgia's story
“Our beautiful daughter Georgia was born in May 2004 - she should be celebrating her 18th birthday this month.
But in October 2016, at the age of 12, our wonderful, happy child passed away after being diagnosed with neuroblastoma. We set up Georgia’s Fund to help fund research into neuroblastoma, and have raised more than £200,000 so far.” Georgia’s dad Richard shares her story.