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.
Lily's story
Lily was diagnosed with stage four, intermediate risk neuroblastoma as a baby.
“Because of her treatment, Lily now has tinnitus and ankle-tightness. She needs to do regular exercises and wear in-soles but she never moans and always gets on with things. Even when she’s in pain, she never complains or gives up. Now at 11 years old, she loves to run, trains every week and wants to be the next Jessica Ennis!” Lily’s mum Angela tells their story.
Pippa's story
Five year old Pippa was diagnosed with intermediate risk neuroblastoma in 2018.
In August 2022, her mum Elisse is taking on the Royal Parks Challenge - trekking 45km, through all 10 of London's Royal Parks, in just one day. Elisse shares their story and tells us why they support Neuroblastoma UK.
Becky's story
Becky was diagnosed with neuroblastoma 50 years ago in 1972. She was 18 months old and was given a one per cent chance of survival.
Thanks to a clinical trial, she is able to share her story today and give families hope for the future.
Charlie’s story
Charlotte was diagnosed with stage 4 neuroblastoma when she was just 12 weeks old. The tumour was wrapped around her spine, crushing the nerves and causing permanent paralysis below the waist. But Charlotte’s determination to succeed has seen her go on to achieve incredible things.
Today, Charlie represents Team GB in basketball and has won medals in the 2018 World Championships and several European Championships and has a degree in Human Biology. This is her inspiring story.
Lauren's story
Lauren was diagnosed with stage four neuroblastoma in 1983, when she was 16 months old. She was given a 10% chance of survival.
Today she says, ‘It is a privilege to share my story. Like Neuroblastoma UK, I also turn 40 this year and I've reached this milestone thanks to the amazing doctors and science that saved me! I’ve been given the gift of being here - now, as a parent myself, I want to give something back to help others.” Lauren tells her own story.
Bethany's story
Just weeks before her 2nd birthday, Beth was diagnosed with stage four high risk neuroblastoma.
But two years after her initial diagnosis and being clear of her cancer for six months, Beth relapsed twice. On Christmas Eve 2019, Beth quietly passed away. She was five years old.
Jill, Beth’s mummy shares their story.
Eva's story
“In February 2016, Eva was diagnosed with Stage 4 neuroblastoma and our life totally changed. She was sadly taken from us in May 2017 aged just seven years old, but her courage, strength and humour were incredible throughout all her treatment.”
Eva’s mum Lauri shares their story.