Georgia's story
personal stories, 40th anniversary Guest User personal stories, 40th anniversary Guest User

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.

Read More
personal stories Guest User personal stories Guest User

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.

Read More
Charlie’s story
40th anniversary, personal stories Guest User 40th anniversary, personal stories Guest User

Charlie’s story

25-year-old 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 her waist. But her determination to succeed has seen her go on to achieve incredible things. This summer, she will be representing Team GB, playing basketball in the Paralympic Games in Paris. Charlotte shares her story here…

Read More
Lauren's story
personal stories, 40th anniversary Guest User personal stories, 40th anniversary Guest User

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.

Read More
Evie's story
personal stories, CCAM Guest User personal stories, CCAM Guest User

Evie's story

Evie was diagnosed with stage L2, intermediate risk neuroblastoma in September 2020, when she was 21 months old.

“Evie has been so resilient, happy and amazing throughout her treatment. But we know things could be so different if we hadn’t taken her to the doctors when we did. One year later, she’s doing really well and is a feisty, energetic 2.5 year old.” Evie’s mum Kelly shares their story.

Read More
Lily's story
personal stories Guest User personal stories Guest User

Lily's story

Lily was diagnosed with low-risk neuroblastoma when she was just over one year old.

By December 2019, Lily was thankfully in remission. We were lucky that she was at an age where she didn’t really know what was going on. We can start to hope for the future and put it all behind us.” Lily’s mum Alex shares their story.

Read More