11-year-old Peter was diagnosed with neuroblastoma in early 2019. Devastatingly he relapsed in August 2020 after being clear of disease for 6 months. His family are fundraising for further treatment either to get Peter back into remission or to try and keep the cancer away if his treatment goes to plan. This could cost hundreds of thousands of pounds. Read more
In January 2021 Flora was diagnosed with Autism Spectrum Disorder, and just three months later her parents were given the devastating news she had high-risk neuroblastoma. Read more
Poppy was diagnosed with high-risk neuroblastoma at just four years old. Her family are fundraising for further treatment, either to get their daughter into remission or to try and keep the cancer away if her frontline treatment does go to plan. Read more
Jacob was just 2 when he was diagnosed with high-risk neuroblastoma, an aggressive childhood cancer that has a 40-50% chance of long-term survival at diagnosis. Read more
Oliver has high-risk neuroblastoma, an aggressive childhood cancer that has a 40-50% chance of long-term survival at diagnosis. His family are appealing for your help to access a clinical trial in New York. Read more
Nellie-Rose is battling a disease no child should have to. She has high-risk neuroblastoma that has a 40-50% chance of long-term survival at diagnosis. Read more
Rupert is battling a disease no child should have to. He has high-risk neuroblastoma, an aggressive childhood cancer that has a 40-50% chance of long-term survival at diagnosis. Read more
Liam's campaign managed to raise an amazing £232,000 in 7 months for Liam to access the Bivalent Vaccine clinical trial in New York. The family will travel in September to start treatment. Read more
Henry has high-risk neuroblastoma, an aggressive childhood cancer that has a 40-50% chance of long-term survival at diagnosis. His family are appealing for your help to raise £163,000 by January 2021. 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 but she was diagnosed with high-risk neuroblastoma Read more
Ewen sadly passed away on 28th September 2020. 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. Thanks to your support, Ashlee is accessing a vaccine in New York with the aim to keep her cancer from returning. 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
“We just want to do everything possible to help our little boy,” says dad, Jordan. Read more
The Mighty Magnus Appeal is urgently asking for your help to raise £225,000 to access the Bivalent Vaccine clinical trial in New York. 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. Thanks to your support, Lauren is now accessing the Bivalent Vaccine clinical trial in New York after raising £234,000! Read more
Seraph has been accessing a vaccine in New York that his family hope will reduce his chances of relapse. He completed the vaccine trial in August 2020. 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
Jake has finished treatment, is showing no evidence of disease, and his family are no longer actively fundraising. Read more
With your support, Maya accessed the vaccine trial in February 2019. Read more
Callum-Lee's mum Nicola shared the devastating news that he passed away on 16th May 2020. Read more
Daya's family raised £362,000 for life-saving surgery in New York Read more
For the past year, Mikey has been accessing the Bivalent Vaccine clinical trial in New York. He completed the clinical trial in April 2020. Read more
We are devastated to share the news that Isaac has sadly passed away. Read more
Breya needs eight PET/CT scans over the two years – not provided by the NHS – which will cost £24,000. Read more
After an amazing fundraising campaign, Ellen began the Bivalent Vaccine clinical trial in June 2019 and completed the trial in July 2020. 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 and in July 2020 Teddy completed the trial. Read more
Kira’s been fighting neuroblastoma since she was 11 years old. Read more
We are devastated to share the news that Jossie has sadly passed away. 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
Phoebe is currently receiving immunotherapy and recently received the amazing news that she is in partial remission. Read more
Lottie has been fighting high-risk neuroblastoma since she was two and a half. Read more
“We’ll never be able to thank everyone enough. You have all helped us to get something that we never thought possible.” Read more
Chloe was diagnosed with high-risk neuroblastoma at just 2 years old. Chloe is now 10 years old and in February 2020 her parents were given the devastating news that she had relapsed for the second time with her disease progressing in February 2021. Read more
Zakky’s family are fundraising in case he needs any further treatment in the future, that isn’t available through the NHS. Read more
By supporting Farid’s Journey, you can help ensure that every possible treatment option is open to Farid should he need it. Read more
Oliver still has a tumour in his head and has never achieved remission but the tumour remains stable. Read more
Raising funds through Kelli’s General Appeal will support Solving Kids' Cancer’s charitable activities. Read more
Dean is a happy, active boy who adores Skylanders and gaming. To his proud parents, seeing him enjoying life is not without complications. Read more
Ruby's mum, Victoria, emotionally announced that her daughter was in remission in late 2017!! Read more
Sam received the amazing news that he had no evidence of neuroblastoma in 2014. Since then he has been living life to the max! Read more
Charlie completed all of his treatment in April 2015 and remains clear of disease. Read more
Luke has been in remission since October 2015. Read more