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
Nellie-Rose is battling a disease no child should have to. She has high-risk neuroblastoma, an aggressive childhood cancer 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 has high-risk neuroblastoma and his family are appealing for your help to raise £232,000 by August 2020. 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 £202,000 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. 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. 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 is accessing a vaccine in New York that his family hope will reduce his chances of relapse. 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
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
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
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
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
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 £202,000 by January 2021.
I'm helping raise funds for little Henry, my husband's school friend's son, with a funny photo contest on Facebook!
I’d like to help to get Henry to New York to continue his treatment x
James has painted his own art work and set up an online art gallery to raise money for Henry the Brave
To support my precious Grandson Liam get to the US for his life saving vaccine in Sept. He is my hero and Little Warrior and always will be. He has been through so much this last year and I am in awe of how he has handled it so well...a real little fighter. Love you lots and lots Ganny Jenny😍😍😍
Ellie wanted to help Liam as he is running out of time and his family are so close in getting Liam a life saving vaccine.Ellie has challenge herself to read 8 books a day to support Liams appeal 💙
I’ve had the pleasure of looking after Henry when he was nursery. He is the most loveable little boys you’ll ever met. His hugs are the best and his love for fireman Sam is what we would spend hours talking about 💙Henry needs your help please help us
Raising future treatment funds for Henry the Brave
Henry's JourneyMy little nephew Henry has high-risk neuroblastoma, an aggressive childhood cancer that has a 40-50% chance of long-term survival at diagnosis.
I recently donated a bone marrow to a small child with leukaemia and just seeing the joy on his face after his surgery changed my life. Children deserve to be just that, children; epitomes and bringers of joy. No child deserves to spend the better years of their life hindered by any kind of illness and so I have decided to help these little angels in whatever small way I can. I hope to bring these children the happiness they deserve
I want this little boy to get the treatment he so badly needs.