In December 2021, five-year-old Dulcie was diagnosed with high-risk neuroblastoma, a rare and aggressive childhood cancer that has a 40-50% chance of long-term survival at diagnosis. Read more
Three-year-old Kayla was diagnosed with high-risk neuroblastoma in May 2021. Kayla’s parents are asking for your help to raise £221,000 by November 2022 for Kayla to enrol on the bivalent vaccine clinical trial in New York that aims to stop her neuroblastoma from coming back. Read more
Jude is a Dinosaur and animal-loving three-year-old. In July 2021 Jude was diagnosed with high-risk neuroblastoma, a rare and aggressive childhood cancer that has a 40-50% chance of long-term survival at diagnosis. Read more
5-year-old Arianna was diagnosed with high-risk neuroblastoma, an aggressive childhood cancer, in November 2021. Read more
Beau was diagnosed with high-risk neuroblastoma, an aggressive childhood cancer that has a 40-50% chance of long-term survival at diagnosis, in December 2020. Her family are appealing for your help to raise £317,000 by May 2022. Read more
Six-year-old Eden was diagnosed with high-risk neuroblastoma, an aggressive childhood cancer that has a 40-50% chance of long-term survival at diagnosis, in April 2021. Read more
Four-year-old Maysaa was diagnosed with high-risk neuroblastoma, an aggressive childhood cancer that has a 40-50% chance of long-term survival at diagnosis, in March 2021. Her family are asking for your support to raise £106,000 by August 2022 for Maysaa to enrol on the DFMO study in Charlotte that aims to stop her neuroblastoma from coming back. Read more
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 asking for your support to raise £152,000 so that Peter can complete the DFMO study in Charlotte, North Carolina. 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. Her family are appealing for your help to raise £312,000 by August 2022 for Flora to enrol on the Bivalent Vaccine clinical trial in New York that aims to stop her neuroblastoma from coming back. 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
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
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. Her family are asking for your help to raise a further £181,000 to reach their fundraising target of £384,000 so Bibi can access a clinical trial in New York that aims to reduce the chances of her neuroblastoma returning. 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
Thanks to your generous support in raising £225,000, Magnus was able to access The Bivalent Vaccine clinical trial in New York. 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
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
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
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
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
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Lilly is the only known case where stage 4s neuroblastoma has relapsed in the brain. Read more
Today, Ryan remains in complete remission. He is now attending school and truly enjoying life. Read more
Lottie and her family travelled to the United States in July 2011 Read more
Joseph was initially diagnosed in January 2013 but is now doing very well. Read more
Amazingly, Mackenzie is now cancer-free - she's been in remission for over five years! Read more