Childhood Cancer Awareness Month
FINDING A CURE FOR CHILDHOOD BRAIN TUMOURS
September is Childhood Cancer Awareness Month and we are taking the opportunity to raise awareness of brain tumours, the biggest cancer killer of children.
We’re working with families to shine a spotlight on this devastating disease. Brain Tumour Research is leading the way to increase the national investment in research to help improve outcomes. And we’re asking you to donate to help us fund the fight and get closer to a cure for brain tumours.
Fact File: Brain tumours in children
- One in three children who die of cancer are killed by a brain tumour
- Brain tumours kill more children than leukaemia
- Symptoms can include headaches, nausea and vomiting, changes in vision and loss of balance
- Treatment depends on the type of brain tumour, size and its location in the brain
- Depending on the circumstances, children diagnosed with brain tumours might be treated with surgery, radiotherapy and chemotherapy or a combination of one or more these
- Medulloblastoma is the most common type of high-grade paediatric brain tumour and occurs more often in boys than in girls
- Diffuse intrinsic pontine glioma (DIPG) is the deadliest form of childhood cancer with a median overall survival of between eight and 12 months
"As a parent told your child has cancer, or a brain tumour, you assume in this day and age there will be something to increase the odds and give you hope. The harsh reality with this tumour is that there are no such treatments.” – Niki O’Dea Patel, Shay’s mum (pictured)
“2020 was a year I could never have imagined in my worst nightmares and to think that someone so small could go through what Aaron’s endured, is inconceivable.” – Nicola Wharton, Aaron’s mum
“I felt complete numbness. The fear that came over me was like nothing I’d ever felt before. It was like I was living somebody else’s life.” – Elaine Paterson, Katie’s mum
We’re leading the way in research to find a cure
Brain Tumour Research is developing a specialist hub focused on paediatric research.
We are building capacity at our established Centre of Excellence at Queen Mary University of London (QMUL). This has been made possible thanks to recent funding commitments which will enable the team to grow in order to facilitate further research into childhood brain tumours.
But we still need your help. Your fundraising and donations support our vital work to fund research at our Centres of Excellence and our campaigning activity to increase the national investment into brain tumour research. You can help us increase our
research capacity further in order to make the breakthroughs that will get us closer to a cure for this devastating disease.
An investment of £144,000 will fund a PhD student joining the team at QMUL led by Professor Silvia Marino and studying the epigenetics of medulloblastoma, the most common type of high-grade paediatric brain tumour. The research will also involve other childhood brain tumours, including ependymoma. This funding has been made possible largely thanks to a generous donation from our Member Charity, The Children’s Brain Tumour Foundation, on closing the charity.
The team will further expand with two of our Member Charities committing to fund two PhD students over a four-year period at a cost of £143,657 each. The William Low Trust has committed to raise the money to fund a researcher who will join the team, developing new strategies to inhibit the progression of aggressive medulloblastoma. A third PhD student is being recruited to undertake research into childhood glioblastoma multiforme (GBM) thanks to funding from Shay’s Smiles.
This increase in research capacity will allow the team to continue working and building on a breakthrough announced in April 2021 in which scientists found a new way to starve cancerous brain tumour cells of energy in order to prevent further growth. These significant findings could lead to a breakthrough in the way that children with medulloblastoma are treated in future.
As part of our programme of activities to mark Childhood Cancer Awareness Month, we have created a special dedication page. Please make a donation in memory of a child lost or in support of the many children and their families who are currently living with this devastating disease. You can share their name and a photograph, alongside a special message.
Matthew, aged 18, who died on 9 September 2021, was passionate about raising awareness of brain tumours. He was first diagnosed in 2006 when he was just three and he endured further treatment last year after his tumour returned. Tragically he was having radiotherapy treatment once again in recent weeks after the cancer spread to his spine.
Help us fund the fight
Your donations and fundraising enable us to build a network of experts in sustainable research at dedicated Centres of Excellence, as well as campaigning to increase the national investment to £35 million a year.
Please donate and help us get closer to a cure for all types of brain tumours, including those which affect children.