Stories of hope
We know the value of hope to families facing their toughest challenge and helping to provide hope to families is a central part of Solving Kids' Cancer UK's mission.
Among the incredibly sad stories, there are also stories of hope, which we are pleased to be able to share and celebrate with you. The stories featured here, shared with permission, are of children and young people who have been diagnosed with neuroblastoma, have completed treatment and are now in remission and doing the things they enjoy most in life.
Some of the children and young people below would have fundraised with Solving Kids' Cancer UK, for access to treatment not available through the NHS and many will have gone on to access and complete treatment overseas. Some families have chosen to keep their child's dedicated fund open for donations. Up until the point at which a child reaches five years post the end of treatment, all funds raised are held for the child for access to treatment and pastoral needs. After this point, funds raised in a child's name are used to support all children and families affected by neuroblastoma through Solving Kids' Cancer UK's activities. If you'd like more information, contact us on 0207 284 0800 or email fundraising@solvingkidscancer.org.uk.
Meet...
Charlotte is now post-treatment and has used what she went through as a child as motivation and inspiration to give back and support children going through what she did.
Tom's experience of neuroblastoma and its lingering effects showcases the resilience that defines his remarkable journey.
Molly's journey through childhood cancer, survival, and the physical and mental after-effects is a testament to her resilience, determination, and the power of self-advocacy.
From confronting childhood insecurities to becoming a passionate advocate for neuroblastoma survivors, Zahra’s transformative journey embodies resilience, empowerment, and hope.
Despite the monumental challenges he has faced since being diagnosed with neuroblastoma when he was young, Louis has not let this hold him back. His inspirational story is one of resilience, character and positivity.
Anya is now at high school and is thriving! Football is one of Anya’s main passions and she is proudly part of a football team
Sassy, unique and kind, 10-year-old Eva loves performing on stage, recreating TikTok dances and making bracelets. Life post-treatment hasn’t come without challenges, but just like she always did during treatment, Eva faces everything with a smile.
14-year-old Peter is a keen gamer and loves all things Lego and playing Minecraft. In January 2024, he completed the DFMO study in Charlotte, made possible thanks to an incredible community of support for his campaign.
Happy, full of life, and a whirlwind of loveliness, Lulu has a great big smile that lights up the world.
Grace was diagnosed with high-risk neuroblastoma in October 2007. She's now 18, and thankfully she continues to do well.
Eight-year-old Poppy loves playing in the park with her friends and her brother. Poppy completed her frontline treatment in October 2022 and scans continue to show no evidence of active disease.
Nellie-Rose is seven, has been in remission since June 2021 and is doing well. She’s smart, funny and full of life despite all she has been through. She radiates happiness and always has a smile on her face.
Liam is a funny, loving and brave eight year old. He loves pizza, painting, football and cars! He enjoys school and playing with his little sister, Kylie.
Lily-Mae has just turned 15. She’s a happy, healthy, normal teenager. She adores singing and dancing and performing arts is her passion. She’s a talented artist, particularly drawing anime and she adores Taylor Swift.
Phoebe is now 18. Phoebe loves spending time with her dogs, family and friends. She enjoys volunteering at the local hospital where she spends time serving tea to the patients in the stroke ward and orthopaedic ward.
Mighty Magnus is now 12! He has been ‘no evidence of disease’ since completing frontline treatment in 2019. He enjoys gaming, playing board games with his family and friends and reading.
Harry Potter and board game fan Lauren has been in remission since 2019. She is now 18, loves travel and music and enjoying life!
Seraph is now nine years old and is doing great, he has been ‘no evidence of disease’ since June 2019. He has endless energy, is getting stronger all the time and is just as messy and noisy as every other child his age.
