Solving Kids' Cancer have launched an emergency fund to help families affected by Neuroblastoma (low, intermediate or high-risk) who are shielding due to COVID-19. Read more
You can Help us Today by making a donation and help us continue our vital work 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
The Alfie’s Wishes Fund at Solving Kids’ Cancer is for anyone who wishes to donate in his memory. The money from this will be used to support referrals providing wishes treats for children with neuroblastoma who sadly have no further curative treatment options available to them. 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
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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. 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
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
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
“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
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
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
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
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
We are devastated to share the news that Jossie has sadly passed away. 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
Getting Chloe to Barcelona
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.
Miss Hallsworth's Reception class are heading out on a sponsored walk to raise money for Chloe
I’m fundraising to help Chloe Balloqui to get the life saving treatment she needs to be cancer free.
Helping Jacob beat cancer and access treatment abroad.
Chloe is dear to my heart and I am passionate about raising money for her to get the help she needs.
I am fundraising for Chloe as I have been following her story since 2013 and would love to see an end to her and her family’s suffering. Neuroblastoma has taken over Chloe’s life and denied her the childhood she should have had. What this poor girl and her family have been through already is unbelievable and I would love to see an end to all their worries and pain. This is the third time Chloe’s cancer has returned and she is desperately running out of options for treatment.
On 31st May Eden, Isla, Jack and Maisy will be cycling 5k to raise money for Our friend Chloe who needs life saving treatment in Barcelona. Any donation, big or small, will be very much appreciated.
Fundraising for Chloe
Instead of birthday presents, I would love my friends to support our brave and lively great niece Poppy in her campaign against the effects of neuroblastoma.
My little niece Poppy was diagnosed with stage 4 high-risk neuroblastoma in July 2020 at just 4 years old.