Chief Executive's Blog

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

Team Chloe - My Football Adventure For Chloe

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.
What if it was your child

Have been following Chloe’s story for a long time and it’s time to join in
Ellie-May’s cutting 10 inches

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. Let’s help Chloe fight this even by donating £1 can help!
Poppy's Campaign

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.

Most read

Lily-Mae, Ireland’s Tiny Dancer, supports Solving Kids’ Cancer

Lily-Mae from Galway, Ireland will be celebrating her 12th birthday this April, but for her parents Judith and Leighton every day is a blessing.
Corey is thriving after neuroblastoma battle

Family donate almost £150,000 to neuroblastoma research
Solving Kids' Cancer welcomes Alexandra Lane to the Board of Trustees

Alexandra Lane was formally voted on and welcomed to our Board of Trustees this week. We are thrilled to welcome Alex to the team.
BEACON study opens in Europe

The much-anticipated BEACON study amendment is now open and recruiting patients.
Steve Richards to step down as Chief Executive

CEO to leave Solving Kids' Cancer after three years in the role.
Solving Kids’ Cancer appoints new Chief Executive Officer

Solving Kids’ Cancer, a national neuroblastoma charity, has appointed Gail Jackson as its new Chief Executive Officer.
Chloe’s Journey

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.
Charities fund new clinical trial

Solving Kids’ Cancer, with Neuroblastoma UK, has awarded a grant of £609,762.40 to enable the SIOPEN High-Risk Neuroblastoma Clinical Trial 2 (HR-NBL2) to open in the UK, it is anticipated to open in early 2021.
Exploring the Statistics Behind Neuroblastoma in the UK

A closer look into the National Cancer Registration and Analysis Service (NCRAS) 2021 report on cancer in children, teenagers and young adults.
First Three Months

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