Author: The Brain Tumour Charity

On 29 February, we stood outside Westminster alongside 34 members of the brain tumour community to launch our campaign calling for a National Brain Tumour Strategy. Read on to find out why.

Inspired by The Big Bake, read Madelaine’s thoughts as she looks back over the last decade of her mum’s brain tumour diagnosis.

We’re driving forward cutting-edge research together, as the Foundation fulfils a ground-breaking new £1.5 million research grant 18 months early.

Recently we were lucky enough to have some time with our wonderful Young Ambassador Rebecca, to explore what being a teenager with a Brain Tumour was like for her.

We’re proud to announce the latest recipients of our Future Leaders grants that’ve been awarded for their innovative new research projects.

Earlier this Brain Tumour Awareness Month we caught up with one of our Trustees, Hayley Conroy, to learn more about the devastating diagnosis experience that her granddaughter, Lily, and family went through. Ahead of the launch of our faster diagnosis report in just two weeks’ time, we are talking about how important a quick, well-supported, and earlier brain tumour diagnosis process is. You can read our previous blog about why we are campaigning on this here.

Our wonderful supporter Tanguy shares his story of why he cycled 55 miles for his son, Maxence.

Kirsty’s Dad Chris, 75, took on a 50 mile walk over 5 days – to mark what would have been her 50th birthday.

Wellness is currently a buzzword in the world of health. But what does it actually mean?

In memory of her sister, lost to a brain tumour, a former director at Bunnyfoot, Becs Gill, is providing invaluable insights to our website redesign and BRIAN projects pro bono as volunteering work.

NHS England has announced a national roll-out of ‘fast-track testing’ to help detect cancer

The 10-year Cancer Plan for England aims to set out a vision and long term approach for cancer services in England until 2032

James was first diagnosed with a brain tumour after having a seizure in 2018. Since then, he has had two awake craniotomies and a string of treatment types. Here, he shares his story on how he has navigated the uncertainty which came with it all.

The Cancer Patient Experience Survey 2021 results show that brain cancer has the lowest rating of care across all cancer sites

A mum-of-two who had surgery to remove a brain tumour counts herself as lucky after her optician encouraged her to have her symptoms investigated.

Phillipa Anders, an Involvement Champion at The Brain Tumour Charity, shares her experience attending the All Party Parliamentary Group on Cancer

Jade Mcmaster, 31, was diagnosed with a brain tumour after having a seizure whilst she was on a petrol station forecourt.

Natasha Tims, 30, from Chard spent the first years of her life plagued by the symptoms of an undiagnosed brain tumour.

Molly Day, 25, from Birmingham spent nearly 12 years of her life living with the undiagnosed symptoms of a brain tumour.

A woman who was diagnosed with a brain tumour last year is encouraging people to get checked if they have symptoms.

NHS data shows waiting time targets for suspected brain cancer in England were missed for the fifth time in last six months.

A family has shared how they are preparing themselves, including their teenage children, for losing their father after he was diagnosed with an incurable brain tumour.

Every patient should have the opportunity to help contribute to the overall goal of meeting the needs of everyone affected by a brain tumour.

A daughter who cared for her mum after being diagnosed with a terminal brain tumour is taking on a sponsored skydive to raise money for The Brain Tumour Charity to help fund vital research to find a cure for the disease.