Podcast thumbnail for Aunty M Brain Tumours Talk Show

Aunty M Brain Tumours Talk Show

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by Claire Bullimore

5.0(5 reviews)
147 episodes
Updated Daily
Accepts GuestsHas SponsorsLocation 🇬🇧
61

Podcast Authority

Beta
GoodBased on show quality, social media presence, reviews, charts, and more
Pod Engine
Quality46
Social94
YouTube76
Engagement68

Podcast Overview

Aunty M Brain Tumours Talk Show - A podcast sharing inspiring stories of brain tumour survivors. Join our supportive community for heartfelt interviews, insights from medical experts, and empowering tales of resilience. Tune in, be inspired, and spread awareness on the path of brain tumour recovery. I’d love for you to join me on the podcast. If you have a story to share, advice to give, or just want to be part of the conversation, please reach out! Your voice could be the one that someone else needs to hear.

Language

🇺🇲

Publishing Since

5/14/2019

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61

Podcast Authority

Beta
GoodBased on show quality, social media presence, reviews, charts, and more
Pod Engine
Quality46
Social94
YouTube76
Engagement68
7
Excellent Areas
1
Good Performance
11
Growth Opportunities
excellent
Episode Length
16 minutes
Performing excellently!
good
iTunes Tags
6.5/10

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Every 19 days

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Recent Episodes

Episode thumbnail for Earlier Brain Tumour Diagnosis: Red Flags Every GP Should Know

March 31, 2026

Earlier Brain Tumour Diagnosis: Red Flags Every GP Should Know

<p>This is the final episode of <strong>Brain Tumour Awareness Month 2026</strong>.</p><p>After 30 days of real people sharing their lived experience of brain tumours, this final conversation asks an urgent question:</p><p><strong>How do we diagnose brain tumours earlier?</strong></p><p>In this special closing episode, Claire speaks with <strong>Dr Victoria McBride</strong>, a GP who has become a passionate advocate for brain tumour awareness after her own family’s experience.</p><p>In 2021, Dr McBride’s nephew Scott was diagnosed with a glioblastoma after repeatedly attending his GP with symptoms that were not recognised as warning signs. By the time he was admitted to hospital, he was critically unwell.</p><p>This conversation explores:<br>• Why brain tumour symptoms are so often missed<br>• The danger of repeated reassurance without proper follow-up<br>• How “headache plus” symptoms can be a warning sign<br>• Why evolving neurological symptoms must not be ignored<br>• The importance of pattern recognition in primary care<br>• The barriers GPs face, including time pressure and lack of continuity<br>• Why earlier diagnosis may not always change prognosis — but can change outcomes<br>• How earlier detection can reduce disability, trauma and crisis admissions<br>• The new toolkit is being developed with <strong>The Brain Tumour Charity</strong> and the <strong>Royal College of GPs</strong> to support earlier diagnosis</p><p>This episode is deeply personal, but it is also practical, hopeful and forward-looking.</p><p>It brings together everything this month has shown us:<br>the missed signs, the delayed diagnoses, the lives changed forever — and the urgent need for better awareness.</p><p>After 31 stories, one truth is clear:</p><p><strong>People know when something is wrong.</strong><br><strong>Patients need to be heard.</strong><br><strong>And earlier diagnosis matters.</strong></p><p>Thank you for listening, sharing, and helping amplify these stories throughout Brain Tumour Awareness Month 2026.</p><p><br></p><p>⚠️ <strong>Content note:</strong> This episode discusses delayed diagnosis, glioblastoma, medical trauma, and the impact of missed brain tumour symptoms.</p><p></p>

Episode thumbnail for Living Fully With an IDH-Mutant Astrocytoma

March 30, 2026

Living Fully With an IDH-Mutant Astrocytoma

<p>Jaime was diagnosed with an <strong>IDH-mutant astrocytoma</strong> — but not in the way anyone would expect.</p><p>After surviving a traumatic brain injury years earlier, Jaime went through scans and rehabilitation to relearn how to walk, talk and function again. It was only much later, after noticing worsening tremors following the birth of her third baby, that more tests revealed something nobody had ever told her before:</p><p>There had been a small mass on her brain all along.</p><p>In this honest and uplifting interview, Jaime shares:<br>• Finding out about her brain tumour completely by accident<br>• The shock of learning something had been seen on earlier scans<br>• Living through watch and wait<br>• Why she pushed for second and third opinions<br>• Choosing laser ablation surgery<br>• Being diagnosed with a grade 2 astrocytoma<br>• Starting Vorasidenib for her IDH-mutant tumour<br>• Seeing her tumour begin to shrink<br>• Living with uncertainty while raising three children<br>• Staying present and finding joy in everyday life Jaime speaks powerfully about advocacy, openness, and making the most of life even when the future feels uncertain.</p><p>Her message is clear:</p><p><strong>Stand up for yourself. Ask questions. Stay present. Book the trip. Get the tattoo.</strong></p><p>This episode is part of a 31-day series sharing real brain tumour stories for <strong>Brain Tumour Awareness Month 2026</strong>.</p><p>If this episode resonates with you, please share it. Every story helps raise awareness.</p><p>⚠️ <strong>Content note:</strong> This episode discusses brain tumour diagnosis, prior traumatic brain injury, surgery, scan monitoring, and long-term uncertainty.</p><p></p>

Episode thumbnail for Where There’s Life, There’s Hope | Elisabeth’s Brain Cancer Story

March 29, 2026

Where There’s Life, There’s Hope | Elisabeth’s Brain Cancer Story

<p>Elisabeth was 35 when a sharp pain in her head woke her in the night.</p><p>What followed was a terrifying chain of events: repeated trips to hospital, being told it was unlikely to be serious, worsening headaches, vomiting, collapse in A&amp;E, and eventually an MRI that revealed a mass on her brain.</p><p>She was alone when she was told.</p><p>It later emerged that for eight days, Elisabeth had been living through a brain haemorrhage.</p><p>In this powerful and deeply honest interview, Elisabeth shares her journey with <strong>glioblastoma</strong> — from diagnosis during COVID, to multiple craniotomies, paralysis down her left side, learning to walk again, radiotherapy, chemotherapy, recurrence, and the reality of living far beyond what many people expect from this diagnosis.</p><p>Elisabeth speaks openly about:<br>• Being diagnosed alone during the pandemic<br>• Her mum fighting to get her transferred to specialist care<br>• The failed biopsy that led to life-saving surgery<br>• Learning to walk again after being left paralysed on one side<br>• Multiple surgeries, radiotherapy and chemotherapy<br>• The exhaustion of treatment while raising two young children<br>• Finding humour in the darkest moments — including “Cancer Carpool Karaoke”<br>• Why she calls the things she looks forward to her “glimmers”<br>• Support from St Christopher’s Hospice and why hospice care needs reframing<br>• Fundraising through music and bringing people together<br>• Choosing to live fully, even in the face of uncertainty</p><p>Elisabeth’s story is raw, funny, heartbreaking and full of fight.</p><p>Her message is clear:<br><strong>Speak up. Ask questions. Keep going. Where there’s life, there’s hope.</strong></p><p>This episode is part of a 31-day series sharing real brain tumour stories for <strong>Brain Tumour Awareness Month 2026</strong>.</p><p>If this episode resonates with you, please share it. Every story helps raise awareness.</p><p>⚠️ <strong>Content note:</strong> This episode discusses glioblastoma, brain haemorrhage, repeated surgery, chemotherapy, radiotherapy, disability, hospice care, and living with a life-limiting diagnosis.</p><p></p>

147 total episodes available

Recent guests on Aunty M Brain Tumours Talk Show

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Imogen

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Steph Still

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Claire Harris

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Israr Jan-Parker

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Vicki

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Maria Peta

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Kiera Mitchell

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Katie Smith

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Madi Ruby

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Matthew White

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What is Aunty M Brain Tumours Talk Show?

Aunty M Brain Tumours Talk Show - A podcast sharing inspiring stories of brain tumour survivors. Join our supportive community for heartfelt interviews, insights from medical experts, and empowering tales of resilience. Tune in, be inspired, and spread awareness on the path of brain tumour recovery.

I’d love for you to join me on the podcast. If you have a story to share, advice to give, or just want to be part of the conversation, please reach out! Your voice could be the one that someone else needs to hear.

How often does this podcast release new episodes?

This podcast updates daily.

Where can I listen to this podcast?

This podcast is available on 9 platforms including Apple Podcasts, Spotify, and more. You can also use the RSS feed directly.

Does this podcast accept guests?

Information about guest appearances is not available.

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