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

73 mile cycle from Brecon Mountain Railway to Upper Brynamman

To rise funds to support a local family to get the treatment for their little boy,
LEJOG for Little Joseph

I am cycling 960 miles over 9 days from Lands End to John 'O' Groats starting August 22nd 2021
Áine McCarthy
WhisperClaims Climbs a Mountain for Peter

We'll be climbing stairs to the height of Ben Nevis to raise money for Peter's Neuroblastoma treatment.

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.
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.
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.
Joseph's Campaign

Joseph was diagnosed with high-risk neuroblastoma in April 2021 at just three years old. His family are fundraising for further treatment, either to get their son into remission or to try and keep the cancer away if his frontline treatment does go 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.
Vivianna's Campaign

Vivianna, or 'Vivi', was diagnosed with high-risk neuroblastoma, an aggressive childhood cancer, at just two 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. This could cost hundreds of thousands of pounds.
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.
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.
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.