Newsletter Signup x
Cancer should never get in the way of a child’s future. Sadly, 2 out of 3 childhood cancer survivors will experience lifelong side effects because of their cancer or its treatment. This Childhood Cancer Awareness Month, you can set up a regular gift, which will help fund research into developing less harmful treatments so that every child with cancer not only survives but can also grow up happy and healthy.
Cancer treatments are developed to target cancer cells and kill them. Unfortunately, they often also impact normal healthy cells in the body which can cause debilitating side effects for young patients. Sadly, 2 out of 3 childhood cancer survivors will be affected by the long-term side effects caused by their cancer or its treatment.
These long-term effects are known as late effects and whilst they will vary from individual to individual, they can include heart conditions, lung damage, cognitive impairment, as well as emotional and mental health issues.
Every child should get to enjoy growing up without suffering from the late effects of their treatment. That is why research into developing kinder and safer treatments, specifically tailored to treating childhood cancer without damaging children’s growing bodies is urgently needed.
This Childhood Cancer Awareness Month, your donation will help fund vital research like this so that every child with cancer not only survives but can grow up happy and healthy. We receive no government funding, meaning without generous supporters like you, research like this may not be possible. Thank you.
Dulcie was just 5 years old when she was diagnosed with cancer. It came as such a shock because cancer was not even on our radar. No one ever expects to hear the words, “Your child has cancer,” but there we were, and in the space of 24 hours, life as we knew it was forever changed. For most of 2021, we were told Dulcie had a condition called ‘impacted faecal matter.
– Debra, Dulcie’s mum
Up until ten weeks old, I was a happy and healthy baby. It all began when my Mum, being a nurse, realised that my vision was not as it should have been, and that I had ‘sunset eyes.’ Of course, this was very alarming for my parents so they took me to my GP to get it checked out. They were advised to take me straight to hospital, where I had an MRI scan, which found a tumour in the centre of my brain. The doctors, who told my parents the news was good, said that the neurosurgeons were expecting me, and my surgery was performed the next morning.
– Libby.
Libby's brain tumour story
Libby’s was diagnosed with a brain tumour when she was just ten weeks old. Now at 19 years old, she shares her story.
Read Libby's storyDulcie's neuroblastoma story
Dulcie was diagnosed with stage 4, high-risk neuroblastoma on 9 December 2021, when she was just five years old.
Read Dulcie's storyWe're here to help so please don't hesitate in contacting us:
info@childrenwithcancer.org.uk | 0800 222 9000 |