
LIGHT UP OUR CHRISTMAS TREE
Light up our Christmas tree and remember a loved one
Light up our virtual Christmas tree and make a donation in memory of a loved one this winter.
Every donation will make our tree sparkle and help fund vital research into neuroblastoma, a rare childhood cancer.
You can let your loved one's light shine with a personalised message and photo.
“We’re adding a light to the tree to remember all the children who have become angels. Knowing our donation will fund research to help more children with neuroblastoma really means a lot to our family.”
Meet the children you’re helping
Your donations can make a huge difference to families of children with neuroblastoma. Read their stories here.
Apollonia (Apple) was diagnosed with stage four, high risk neuroblastoma on 9th August 2021. She has been in remission since November 2022 and is a happy, healthy six year old. “Thanks to the research funded by Neuroblastoma UK, our Apple has a chance now.” Anthea, Apple’s mum, shares their 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.
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.
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…
George, aged three, was diagnosed with stage four neuroblastoma in April 2020.
“When George was diagnosed, it really helped to read positive stories so I hope our story helps other families like ours to see it’s not all doom and gloom.” His mum Roxanne shares their story.
On this important day, we would like to share with you a story about a beautiful little boy, Spencer, who sadly passed away in 2007 from neuroblastoma. Spencer’s mum, Amanda, has kindly shared this story to help raise awareness about the drastic need for new, more effective and less punishing treatments for neuroblastoma.
Hayley has kindly shared a heart-warming story about her son, Alex, who was diagnosed with neuroblastoma at the age of two. Alex’s story demonstrates just how important treatments and research can be for the lives of children with neuroblastoma and their families.
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.
Isobel, Cara’s mummy, shares their story to help other parents spot the signs of this cancer earlier.
Zahra was diagnosed with neuroblastoma when she was just two weeks old. Now 21, she recently graduated with a law degree! This Childhood Cancer Awareness Month, Zahra shares her story to help other families currently experiencing neuroblastoma. “If my story can offer solace, inspiration, or guidance to just one person or family, I find immense fulfilment in knowing that my experiences have made a positive impact. “
George, aged three, was diagnosed with stage four neuroblastoma in April 2020.
“When George was diagnosed, it really helped to read positive stories so I hope our story helps other families like ours to see it’s not all doom and gloom.” His mum Roxanne shares their story.