Dr Tyler Miller was one of our Future Leaders. Now a Junior Fellow, he manages a team of 12 at his own lab. 

Here he explains how this team is trying to figure out how to prevent our own immune cells from suppressing our immune system. Instead, he aims to turn part of a brain tumour's immune system - myeloid cells - into an effective army of immune agents that can both kill tumour cells and attract new recruits, like the T-cells Mat mentioned, to target the tumour.

You can read more about this here

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Welcome to a new series of very short episodes of The Brain Tumour Charity podcast in which you’ll get to know key people in the brain tumour community.  

The first part of the series is called Meet The Researcher and it's based on a webinar we hosted in 2025 that was all about immunology.  

We’re kicking it off by introducing you to someone who’s trying to figure out how our body’s natural defence mechanisms can help fight the aggressive brain tumour glioblastoma.  

You can find out more about our Future Leaders programme and Dr Mat Clement's work here. We wish him the best of luck with the incredible work he's doing. 

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At a reception in Westminster on 15th December, The Brain Tumour Charity released its report into the cost of a brain tumour diagnosis. The report makes the economic case for a National Brain Tumour Strategy to minimise these costs - both to the individual and to society. We unpick this report with Marcus Loney-Evans, Head of Policy and Campaigns at The Charity.

You can read the full report here.

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The Brain Tumour Charity has released its report into the staggering cost of a brain tumour diagnosis to the UK economy. The report makes the economic case for a National Brain Tumour Strategy to minimise these costs - both to the individual and to society. 

In part one of this episode, Anna unpicks some of the report's findings with Kimberley, who's living with a brain tumour diagnosis and Rhiannon, who's caring for her son following his ill-health. They discuss the impact on their own finances. 

In part two, Chandos interviews Marcus - Head of Policy and Campaigns at The Charity - to dig deeper into the report's finding's.

To find out more, you can download a copy of the report on the charity's website.

Thank you for listening. 

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Hosts Anna and Andy mark two years since Dr Michele Afif became Chief Executive at The Brain Tumour Charity by asking about her early life, her previous careers in medicine and law - and a few more questions that we crowdsourced from our listeners. 

In response, Michele explains how she's focused The Charity on turning its co-created strategy into a 'strategy in action'. She's honed in on what it needs to deliver, what evidence backs that up and how it can deliver truly transformative results. 

She describes it as asking the question: "How do we push one or two big boulders up the same hill rather than hundreds of boulders up hundreds of hills?"

Michele also talks about her proudest moments, her biggest challenge, The Charity's imminent plans and the advice she'd give her younger self. 

And if you have any questions for Michele or The Charity, you can email [email protected]

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In this episode, we'll hear from four of our much-valued Involvement Champions : Rebecca, Oriana, Claire and Mark.

We recorded their presentations to the whole organisation as they explained why they wanted to become key voices in the  brain tumour community.  (Trigger warning, they talk about diagnosis and mental health issues, and their stories are very moving.)

Then our host Anna Blyszko - a former Young Ambassador herself - quizzes The Brain Tumour Charity’s Involvement Manager, Rachel Roberts, about what exactly our Involvement Network aims to achieve and why we've launched a new initiative called The Listening Project.

If you're interested in becoming an Involvement Champion, recruitment for the next cohort begins in late summer 2025. You can find out more here.

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After weeks of toil and training, The TCS London Marathon 2025 is just around the corner and The Brain Tumour Charity has 145 runners taking part this year - more than ever before! 

Our Involvement Champion Imelda Turnock speaks to two of them - Barbara Prodger and David Barrow - about their reasons for running.

But first, Andy Tudor gets some insider tips from our man at JustGiving. 

Sam Gurry delves into the data to explain how anyone taking part in a charity challenge can maximise their fundraising. From personalising your story to the optimum number of times to post about your challenge on social media, to gamifying fundraising and incentivising donors - we get the low down.

If listening to this sparks an interest in taking part in one of our events, you can find them all listed here.

Hosts: Andy Tudor and Imelda Turnock.

Audio editors: Jo Porter and Elliot Broad

Producer: Jo Porter

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Our focus in this episode is on friendships and close bonds. How does a brain tumour diagnosis affect our loved ones and who can we turn to for support or advice when we don’t want to worry or upset those closest to us?   

To answer that question, Andy Tudor talks to five women who were all treated at the same hospital for the same meningioma diagnosis but who only met through one of The Brain Tumour Charity’s online peer support groups. They describe that group as "invaluable", "a lifeline" and as "each other's aftercare." 

What's more, four of them have teamed up to take on The Twilight Walk together on 22 March - roping in some of their relatives too! Their efforts will mean The Charity can continue to fund things like our support services as well as much needed research into brain tumours. This is the Brighton Brain Aches fundraising page.

We'd also like to the thank the Puzzle Bored Cafe in Brighton for allowing us to record this episode in their Quiet Room. 

Audio Editor: Elliot Broad

Producer: Jo Porter

Contact: [email protected]

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If you or someone you know needs a listening ear, you can contact our Support Team by calling 0808 800 0004, by using the web chat on our website or by emailing [email protected]

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A warm welcome to Let's Talk About Brain Tumours!

After a break since the summer, we're back to bring you interesting and informative conversations with members of the brain tumour community and at The Brain Tumour Charity.

A new production team is now at the helm, so bear with us while we learn the ropes of podcast production. But we're delighted that our volunteer co-hosts remain unchanged: Anna Blyszko, Chandos Green and Andy Tudor.

"On the cusp of change...!" today, Anna and Chandos quiz Anna Jewell and Cameron Miller about how the Less Survivable Cancers Taskforce was set up, what it's achieved and what its latest campaign is about. Then, Andy meets Frankie Davies whose mum Sue's story throws that campaign into sharp relief.

Many thanks to all our guests for taking part in this recording.

Further information

• Frankie mentions online support groups and you can find out about these here 
• To find out more about the campaign go here or search the hashtags #LessSurvivableCancersAwarenessWeek #CloseTheDeadlyCancerGap on social media
• If you have any questions about this episode or want to find out more about this podcast, you can email the team at: [email protected] 

Producer: Jo Porter
Audio editor: Elliot Broad

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If you or someone you know needs a listening ear, you can contact our Support Team by calling 0808 800 0004, by using the web chat on our website or by emailing [email protected]

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Anna talks to Anna Solth and Victoria Wyes about their experiences of being neurosurgeons and women in the field of neuroscience.  They share their passion for neuroscience, discuss the work they are doing now and their plans for the future.

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If you or someone you know needs a listening ear, you can contact our Support Team by calling 0808 800 0004, by using the web chat on our website or by emailing [email protected]

If you have any questions about this episode of the podcast, email [email protected]