Our blogs

Chief Executive's Blog

Gail Jackson joined Solving Kids' Cancer in April 2020, she writes a regular blog of her experience as a charity leader.

Family Support

Blogs from Solving Kids' Cancer's Family Support Team

Research Blog

Solving Kids' Cancer's Research Team blog

Latest

Eden's Fundraising Pink Day

We are organising a PINK DAY fundraising event on Thursday 10th March which is also Eden’s 7th birthday and pink is her favourite colour. Therefore, it will simply involve wearing something pink and bringing a monetary donation to your school, college, business and/or workplace.

Some schools, colleges and businesses might consider additional fundraising opportunities on the day to raise further donations, such as games, cake sales, competitions and/or enterprising events.
Relapse Prevention Therapies: an in-depth look

In this special edition of our research blog, Research Director and Chair of Trustees Nick Bird looks at the landscape of maintenance therapies and their accessibility in the UK.
Aberlady Social Joggers

Fundraising for Flora's Fight from here running friends in Aberlady
Yorkshire 3 peaks for Beau

To get Beau to Sloan.

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.
Joseph Yeandle

We are devastated to share the news that beautiful Joseph has sadly passed away.
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.
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.
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.
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 fundraising for further treatment either to get Peter back into remission or to try and keep the cancer away if his treatment goes to plan. This could cost hundreds of thousands of pounds.
Ollie Sweeney

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

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.