Meet Andrew, who is taking on a 3 month cycling tour of Japan to raise funds.

The Ways Ahead project aims to find ways to support, and improve quality of life for those diagnosed with a lower-grade brain tumour. It also explores ways to help friends and family who are supporting those diagnosed.

On World Brain Tumour Day this year, we’ll be joining the call to raise greater awareness and understanding of brain tumours – to help people like Kimberley dealing with a brain tumour diagnosis.

This Volunteers’ Week, we’re spotlighting some of our amazing Involvement Volunteers and giving them the opportunity to share what volunteering means to them!

Extracts from Nicola Nuttall’s book – The Stars Will Still Be There

We are pleased to announce the two researchers who have been awarded our latest Expanding Theories grant!

14 months after she first went to hospital, Simrat, 22, was told the news she longed to hear. She was in remission! Here’s her story.

Ed, one of our Young Ambassadors, explains how losing his mum following her brain tumour diagnosis affected his mental health.

Francesca, one of our Young Ambassadors, explains how her mental health was affected after becoming a carer for her boyfriend when he was diagnosed with a brain tumour.

What happened to the £40m of Government funding that was committed to research into brain tumours in 2018?

Find out how our 2024 Machu Picchu team got on, and how their fundraising will improve the lives of everyone affected by brain tumours.

Meet Kit Vincent who created the film Red Herring. In turning the cameras on himself and his loved ones, Kit processes his own brain tumour diagnosis. The film is being screened at selected cinemas from 3 May and is also available for streaming at home.

Wickes and The Brain Tumour Charity celebrate this incredible landmark sum after collaborating on a series of fundraising missions across its 230 stores and digital channels as part of a two-year partnership

Nicola Durrant, from Oxfordshire, will raise funds at her Open Studios event in May – after losing brother Stephen, and husband David, to the same brain tumour type, ten years apart.

Research that we funded nearly 20 years ago laid the foundations for last week’s approval of dabrafenib and trametinib to treat childhood gliomas.

More than 52,000 of you joined our call for a National Brain Tumour Strategy and now Parliamentarians across the political spectrum have added their support.

Meet some of the intrepid people running this year’s London Marathon in support of The Brain Tumour Charity.

Our open letter to the Government calling for a National Brain Tumour Strategy has been a huge success – but we’re not slowing down yet!

CAR-T cell therapy is a type of immunotherapy that may be promising for treating brain tumours. There is lots of research in this field across the globe and it may one day be used more widely to treat this devastating disease.

Meet Simon and Ella and learn why they believe a National Brain Tumour Strategy is a No Brainer!

We pay tribute to The Wanted’s legendary singer, this Brain Tumour Awareness Month

The Twilight Walk London was a roaring success thanks to the passionate brain tumour community who united to raise an incredible £338k so far.

This Brain Tumour Awareness Month we held three events in the parliaments of Scotland, Wales and Westminster. Highlighting our new It’s a No Brainer campaign and enabling volunteers to share their experiences with policymakers.

The Brain Tumour Charity are delighted to announce a new partnership with two Family Led Charities that share the same aims of improving outcomes for children diagnosed with high grade brain tumours