We’re excited to announce that we’ve appointed Dr Simon Newman as our new Chief Scientific Officer.

Neil and Angela Dickson have been awarded OBEs in recognition of their dedication to establishing the world’s largest brain tumour charity

Five years on, Nikki Saunders shares her experience of both her mum and brother being diagnosed with a glioblastoma.

Rebecca Taylor, a Young Ambassador from 2021-23, shares her experience of being a Young Ambassador for The Brain Tumour Charity.

Thorngrove School in Berkshire chose to support The Brain Tumour Charity after pupil, Ned, was diagnosed with a brain tumour.

Five year old Mercy is battling an incurable brain tumour. Her family are crowdfunding for £100,000 for medication from abroad.

An update from our Policy and Campaigns team following an exciting week in Scotland.

We are pleased to announce that The Brain Tumour Charity has joined the Cancer Tech Accelerator 3.0 as a new funding partner!

Recent research suggests that there could be a new treatment on the horizon for some children diagnosed with low and high-grade gliomas.

An update on the Scottish Steering Committee’s new objectives and next steps.

“On most of our walks, we met people who have been affected by brain tumours.”

CRUK has just launched a manifesto with five priority actions for the next government. We take a look at how they align with the needs of the brain tumour community.

Amy, one of The Charity’s Young Ambassadors, talks about her mum’s brain tumour diagnosis and how she’s raised money in her memory.

Come with us as we look back at some of the ways you, the brain tumour community, has given the gift of time in 2023.

The Northern Joe Cup is now in its third year and this year the event is even bigger and better with a full week of squash-related activities and fundraising.

If you or a loved one has a brain tumour diagnosis, the spirit of the season might be more important than ever. Here are some ideas for getting festive with family and friends.

Two of our funded researchers have won awards at the Society for Immunotherapy of Cancer (SITC) annual conference!

Georgina Johnstone, from Harrogate, was just one when she was diagnosed with a brain tumour last September. Now her family are raising awareness of brain tumour symptoms to help others spot the signs.

We recently attended the NICE 2023 conference and share some of the key takeaways we gathered from the event.

Natalie McKenna-Mounty was diagnosed with a glioblastoma in 2020, her tumour returned in June this year, and now she is supporting our new research funding to find better glioblastoma treatments.

Virtual gifts are shaping up to be a popular choice this Christmas. We take a look at why that is, what virtual gifts are, and how you can order and send them!

We are pleased to announce the two researchers who have been awarded the Junior Fellowship grant – the second award in our Future Leaders programme!

In this guest post, supporter Claire Watling talks about the support she received from The Charity after her husband Peter’s diagnosis and during his illness, and the value of Gifts in Wills.

Catrin George-Carey was diagnosed with a rare brain tumour in March 2022. Now back at work following successful surgery, she’s highlighting the brain tumour symptoms that she initially brushed off – so that others don’t do so!