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Henry has high-risk neuroblastoma, an aggressive childhood cancer that has a 40-50% chance of long-term survival at diagnosis. Read more
Ollie’s mum and dad are determined to do everything they can to give him the best possible chance of beating neuroblastoma Read more
At the age of just two, Beatriz suddenly became very clingy and unhappy. Her parents thought it was just a phase. Read more
Ewen is a happy and restless boy who runs everywhere. He loves trucks, cars and blowing dandelions. But this amazing little boy has had his childhood interrupted by childhood cancer. Read more
Ashlee was diagnosed with high-risk neuroblastoma at the age of six but relapsed for the second time in November 2018, devastating her family. Read more
Katie Rose's family continue to ask for your help and support to raise funds, to give her the best chance of living cancer-free. Read more
Jasmine sadly passed away on December 24 2019. Read more
We are devastated to share the news that brave William has sadly passed away. Read more
Oliver's family shared the devastating news that their brave, beautiful boy passed away on 16th November 2019. Read more
Aaron was a happy young man, full of energy and banter. Read more
“We just want to do everything possible to help our little boy,” says dad, Jordan. Read more
Glow gold with us this September Read more
Join the fight against neuroblastoma this Christmas. Read more
The Mighty Magnus Appeal is urgently asking for your help to raise £225,000 Read more
Freddie's family shared the devastating news that he passed away on 3rd December 2019. Read more
This is Lauren, a typical 13-year-old who loves reading books and writing stories Read more
Seraph is an extremely cheeky little monkey, as many four-year-old children are. Read more
Denver was a happy, cheeky three-year-old boy. He passed away in February 2019 after battling neuroblastoma for months. Read more
Oliver is accessing treatment in New York that his parents hope will reduce the chances of his cancer coming back. Read more
“We cannot thank you all enough for helping us to reach this target, we are so so grateful to each and every one of you for making this possible” Read more
Luke sadly passed away in December 2018 Read more
Jake has finished treatment, is showing no evidence of disease, and his family are no longer actively fundraising. Read more
Maya is accessing the Bivalent Vaccine in New York but still desperately needs your help to raise the funds to finish it. Read more
He has suffered three relapses in January 2017, August 2018 and most recently in May 2019. Read more
“I am heartbroken to say that we lost our beautiful baby bear today. The world is a much sadder place. Our love for each other will live on forever.” Read more
Hayley was a happy little girl, who was healthy until she was diagnosed at the age of four with high-risk neuroblastoma. Read more
Daya's family raised £362,000 for life-saving surgery in New York Read more
Jessica was an inspirational, brave girl who passed away peacefully at the age of eight. Read more
Mikey is currently accessing the Bivalent Vaccine clinical trial in New York Read more
Isaac is adored by everyone who has met him, especially his little brother. Read more
Breya needs eight PET/CT scans over the two years – not provided by the NHS – which will cost £24,000. Read more
Stanley George may have only been with us for two years and 11 days but his amazing smile and wonderful character touched the lives of many people. Read more
All money raised by the Oscar Knox Fund will be ring-fenced by Solving Kids’ Cancer to help find and fund promising new therapies. Read more
Ellen is accessing a vaccine in New York that her family hope will reduce her chances of relapse. Read more
Reuben’s family received the amazing news that he was cancer-free in January 2018 and chose to take him to New York to receive a clinical trial called the Bivalent Vaccine Read more
Teddy’ family fundraised to be able to access a vaccine in New York Read more
Vanessa was an inspiring young lady who sadly passed away after bravely fighting neuroblastoma for over nine years. Read more
Kira’s been fighting neuroblastoma since she was 11 years old. Read more
Jossie has been fighting high-risk neuroblastoma since November 2017 Read more
Little Morgan was a busy child, always having fun. He passed away after a three-year neuroblastoma fight in January 2018. Read more
Thanks to your kindness and generosity, Isla travelled to New York for the Bivalent Vaccine in March 2018 and completed the treatment in March 2019. Read more
Jacob’s family have decided to keep his fundraising page open for those wishing to donate or fundraise in his memory. Read more
Stanley’s parents have created a fund at Solving Kids’ Cancer to raise money in memory of their gorgeous son. Read more
Phoebe is currently receiving immunotherapy and recently received the amazing news that she is in partial remission. Read more
Phelan was a cheeky, outgoing little boy who passed away in September 2017. Read more
Lottie has been fighting high-risk neuroblastoma since she was two and a half. Read more
Eileidh was a bright, sociable, independent and stubborn girl, who loved Minnie Mouse, Frozen and Sofia the First. Read more
We are fundraising to help Ashlee reach her target of £239,000 to have life saving cancer treatment in New York
I am helping to raise money to get Ashlee to New York for treatment
Katie & Hannah are Ashlee’s friends. They are trying to get as many people as possible to donate £1 to help raise funds to get Ashlee to New York for treatment.
Ashlee is a pupil at my school and I am getting involved with raising funds to help with her treatment.
We want to help our friend Ashlee to raise the funds she needs to get the vaccine to stop the cancer coming back. We are going to Walk to Waterbeach along the River Cam on Saturday 1 February.
Myself, Kerri, Lauren, Kelly, Lyndsay and Joyce are all doing the Looney Dook on 1st January, 2020 to help raise money for Ashlee
Erin and Ciara, age 7, will be cutting their hair and donating it to the Little Princess Trust to make a wig, on the 7th January and getting sponsored to do so for for Ashlee's Appeal.
Running the London Landmarks Half Marathon in memory of Grace, a wonderful and special little girl who lost her fight against cancer this year.
We are doing the Looney Dook on New Years Day to raise funds to help Ashlee
Ashlee is a pupil at my school who is suffering from a rare form of cancer called neuroblastoma.