Chief Executive's Blog

In the latest edition of her blog our CEO, Gail, shares her experience of being part of the National Neuroblastoma Nursing Group, made up of cancer nurse specialists and research nurses. Read more

Together, We Are Stronger

In the latest edition of her blog our CEO, Gail, reflects on what it means to be part of a parent-led charity. Read more

New Year, New Opportunities

In her latest blog our CEO, Gail Jackson reflects on entering a new year and what 2021 and beyond may bring for the charity. Read more

Celebrating Success and Acknowledging Challenge

Our CEO, Gail, reflects on 'Pandemic Fatigue' and the importance of celebrating success in the face of challenge. Read more

First Three Months

Gail Jackson, CEO, launches her blog. Reflecting on personal resilience, our work and joining Solving Kids' Cancer as COVID hit. Read more

Latest

Ronin's Spidey Hike

Ronin is doing a 3 mile hike home from playgroup on the last day of term to raise money for his cousin Flora. He will be dressed up as Spiderman!
Ronin loves walking and would like to help raise lots of money for Floras treatment in America

Thankyou so much for any donations
Family Support Coordinator

Solving Kids' Cancer is looking for a Family Support Coordinator to join the Family Support Service
Judes birthday fundraiser

To help Jude get to America to get the next step of his treatment ❤️
Rother Valley Sponsored Walk #ForJude

We are doing a sponsored walk to raise money to get Jude to America for additional cancer treatment

Beau's Campaign

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.
Flora's Campaign

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.
Joseph Yeandle

We are devastated to share the news that beautiful Joseph has sadly passed away.
Jude's Campaign

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.
Maysaa's Campaign

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.
Chloe’s Journey

Beautiful Chloe passed away on the 4th of February 2022.
Eden's Campaign

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.
Peter's Campaign

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.
Kayla's Campaign

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.
Ollie Sweeney

Ollie's family shared the devastating news that their beautiful boy passed away on Sunday 18th July 2021.

Chief Executive's Blog

Solving Kids' Cancer meets Google

Heroes Are Made by the Path They Choose

Working Together

Together, We Are Stronger

New Year, New Opportunities

Celebrating Success and Acknowledging Challenge

First Three Months