Other sources of help

It’s important to Solving Kids’ Cancer that we work closely and collaborate with other charities that offer support and distribute useful information to families affected by neuroblastoma. Here’s a list of useful links to other organisations that share our goal of improving the lives of everyone affected by neuroblastoma.

Children’s Cancer and Leukaemia Group (CCLG)

CCLG coordinates research and care for children and their parents. There are 21 CCLG specialist centres for the treatment of childhood cancer and leukaemia, covering all areas of the UK and Ireland. The website also has information about the CCLG, childhood cancer and leukaemia.

Children’s Neuroblastoma Cancer Foundation (CNCF)

CNCF is an American neuroblastoma foundation who have supported Solving Kids' Cancer, particularly with our conferences. Follow this link to read their very detailed and informative handbook for parents.

Neuroblastoma UK

The Neuroblastoma Society is Britain’s longest-standing neuroblastoma charity. They are mostly concerned with funding research and providing clear information for families.

Children with Cancer

Children with Cancer invest millions of pounds every year in essential research, welfare and campaigning programmes for children and young people suffering from cancer, as well as raising awareness. They provide days out for children, coordinate hospice care and can provide financial assistance for families.

CLIC Sargent

CLIC Sargent provides nurses and social workers to aid in the care of children and young people with cancer. At diagnosis, each family will be assigned a CLIC Sargent social worker who is there to provide practical and emotional support for families affected by neuroblastoma.

Macmillan Cancer Support

Provides free information and emotional support for people living with cancer, and information about UK cancer support groups and organisations. Also offers free confidential information about cancer types, treatments and what to expect.

The Royal Marsden

The Royal Marsden is a world-leading cancer centre specialising in diagnosis, treatment, care, education and research.

Latest

Cross-party MPs back calls for a UK-led vaccine trial to help children with cancer
Kathryn's RSR for Jude

To help Jude's family reach their fundraising target.
St Mary Magdalene - Y5 and Y6 Ticket Sales
Leah Ambler- Research Officer

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 £252,000 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.
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.
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. Thanks to your incredible fundraising and support, Peter was able to enrol on the DFMO study in Charlotte at the end of January 2022.
Dulcie's Campaign

In December 2021, five-year-old Dulcie was diagnosed with high-risk neuroblastoma, a rare and aggressive childhood cancer that has a 40-50% chance of long-term survival at diagnosis.