Coronavirus (COVID-19)

Please find below the latest guidance on coronavirus for children with neuroblastoma, information on our Emergency Fund for families and details on how you can support the charity through this time.

Help us Today Appeal

You can Help us Today by making a donation and help us continue our vital work. Read more

Emergency Fund for Families

If your family is facing financial strain due to the impact of the Coronavirus pandemic you can make an application to our Emergency Fund. Read more

A Message from Nick Bird, Chair of Trustees

A Message from Nick Bird, Chair of Trustees Read more

Important Update - Shielding Guidelines

The Government have confirmed revised amendments to the shielding guidelines for children and young people [0-18 years]. Read more

Emergency Fund Frequently Asked Questions

Emergency Fund Frequently Asked Questions Read more

Latest

12 hr cycle for Flora - Sunday 25th July 2021

In January 2021 Flora’s parents were given the devastating news that at just 2 years old she had high-level Neuroblastoma, an aggressive childhood cancer.
The 5k Run For Chloe

It is for Chloe to get to Barcelona for her life saving treatment.
Working Together

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.
Tough mudder and 250 miles for flora

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.
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.
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.
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’s Appeal

Ollie’s mum and dad are determined to do everything they can to give him the best possible chance of beating neuroblastoma.
Corey is thriving after neuroblastoma battle

Family donate almost £150,000 to neuroblastoma research
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.
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.
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.
Nellie-Rose's Campaign

Nellie-Rose is battling a disease no child should have to. She has high-risk neuroblastoma that has a 40-50% chance of long-term survival at diagnosis.