The GlioBabes

Mel and Mol
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  • Self-Improvement
  • Updated Weekly

The GlioBabes Podcast. Real talk from young women living with brain tumours in their 20s. Unfiltered chats on health, identity, and life turned upside down, coming to you with dark humour and the raw unfiltered truth. Join Mel and Mol - and some special guests - weekly on your favourite podcast platforms.

  1. 6d ago

    S8. Ep. 3: In Conversation With Linda Radosinska | NeuroSpicy Art

    The GlioBabes, a podcast created by two young women who were both diagnosed with brain tumours at a young age. Mel and Mol are creating a safe space to talk about their experiences and to raise awareness of brain tumours and ill health within the young population. Welcome back for Season 8! The season we returned back to the community to bring on guests impacted by brain tumours in all different ways, kindly sharing their experiences and lessons along the way. From various grades to positions, living beyond to grieving, we are here to talk about it all. In episode three, we are joined by Linda Radosinska. Linda is a Melbourne-based artist, creative director, and TEDx speaker. After surviving brain surgery in 2025, she created NeuroSpicy Art, a vibrant 109-piece collection celebrating the brain, creativity, and neurodiversity. Through her work, Linda raises funds for brain cancer research while inspiring conversations about science, art, and what it means to be human. Check out the project and even get your own piece at www.neurospicyart.com 100% of the profits from the ‘Neurospicy Art’ collection will support brain cancer research in Australia, between The Mark Hughes Foundation and Cure Brain Cancer Foundation. The episode is now available on Spotify, YouTube, Apple Podcasts and Amazon Music. Support links: The Brain Tumour Charity Call 0808 800 0004 Monday - Friday 9-5 Email support@thebraintumourcharity.org Young Adult team YAS@thebraintumourcharity.org Phone as above 0808 800 0004 and ask for The Young Adults Service Brain Tumour Support https://www.braintumoursupport.co.uk/ Samaritans (24/7UK wide) – 116 123 In an emergency, visit A&E or dial 999 Australia Specific Support Lines: Brain Tumour Alliance Australia www.btaa.org.au Cure Brain Cancer Foundation www.curebraincancer.org.au Mark Hughes Foundation markhughesfoundation.com.au Please don't be alone. We are here for you. Spotify, YouTube, Amazon Music, Apple Podcasts: @TheGlioBabes Instagram: @thegliobabes TikTok: @the.gliobabes LinkedIn: The GlioBabes Podcast *music by: SKIRK - soundcloud.com/skirkofficial Our guests share their personal experiences and opinions. We understand that everyone’s journey is unique, and what resonates with one person may not with another. We encourage open-mindedness and respect for diverse perspectives.

    34 min

  2. Jun 12

    S8. Ep. 2: In Conversation With Chris Rigg | Unmethylated Glioblastoma: Calling For Justice

    The GlioBabes, a podcast created by two young women who were both diagnosed with brain tumours at a young age. Mel and Mol are creating a safe space to talk about their experiences and to raise awareness of brain tumours and ill health within the young population. Welcome back for Season 8! The season we returned back to the community to bring on guests impacted by Brain Tumour in all different ways, kindly sharing their experiences and lessons along the way. From various grades to positions, living beyond to grieving, we are here to talk about it all. In episode two, we are joined by Chris Rigg. Chris shares his personal experiences of living with glioblastoma, including treatments he has accessed privately outside the NHS. The views expressed are his own and should not be taken as medical advice. Anyone considering treatment options should discuss them with their healthcare team. When Chris was told he had glioblastoma, one of the most aggressive forms of brain cancer, his first reaction wasn’t fear. It was anger. Two and a half years later, the 52-year-old father of three is still here challenging the systems he believes fail brain cancer patients at their most vulnerable moment. Talking on his own experiences and views of the systems he’s faced, Chris gives us his time to share his truth. After a violent seizure at home, breaking three vertebrae in his spine, he was sent away. After a second seizure in front of his son, Chris was diagnosed with unmethylated GBM4, a terminal diagnosis of brain cancer with a poor prognosis. Chris currently receives his treatment in Germany and uses the device Optune, not recognised in the UK on the NHS. You can see Chris wearing the device in this episode. This episode is tough, so please take care of yourself. Helplines are, as always, below. The episode is now available on Spotify, YouTube, Apple Podcasts and Amazon Music. Support links: The Brain Tumour Charity Call 0808 800 0004 Monday - Friday 9-5 Email support@thebraintumourcharity.org Young Adult team YAS@thebraintumourcharity.org Phone as above 0808 800 0004 and ask for The Young Adults Service Brain Tumour Support https://www.braintumoursupport.co.uk/ Samaritans (24/7UK wide) – 116 123 In an emergency, visit A&E or dial 999 Please don't be alone. We are here for you. Spotify, YouTube, Amazon Music, Apple Podcasts: @TheGlioBabes Instagram: @thegliobabes TikTok: @the.gliobabes LinkedIn: The GlioBabes Podcast *music by: SKIRK - soundcloud.com/skirkofficial Our guests share their personal experiences and opinions. We understand that everyone’s journey is unique, and what resonates with one person may not with another. We encourage open-mindedness and respect for diverse perspectives.

    58 min

  3. May 29

    S8. Ep. 1: In Conversation With Dr Scott Arthur MP | The Rare Cancers Act

    The GlioBabes, a podcast created by two young women who were both diagnosed with brain tumours at a young age. Mel and Mol are creating a safe space to talk about their experiences and to raise awareness of brain tumours and ill health within the young population. Welcome back for Season 8! The season we returned back to the community to bring on guests impacted by Brain Tumour in all different ways, kindly sharing their experiences and lessons along the way. From various grades to positions, living beyond to grieving, we are here to talk about it all. In episode one, we are so very excited to have Dr Scott Arthur, a Labour Member of Parliament (MP) for Edinburgh South West, elected in July 2024. His landmark achievement is The Rare Cancers Act, which he introduced as a Private Members' Bill and successfully steered into UK law in early 2026. After Scott’s Father-in-law was diagnosed with glioblastoma (grade 4 brain tumour, 12-18 month prognosis) he understood this landscape on a personal level. Wanting to do more for brain tumours he found a way to develop the Rare Cancers Bill, which has newly had royal ascent and become an act. In such incredible timing for Scott to join us today to talk about the journey and lessons learnt along the way. Instagram: @dr.scott.arthur Tiktok: @drscottarthurmp The episode is now available on Spotify, YouTube, Apple Podcasts and Amazon Music. Support links: The Brain Tumour Charity Call 0808 800 0004 Monday - Friday 9-5 Email support@thebraintumourcharity.org Young Adult team YAS@thebraintumourcharity.org Phone 0808 800 0004 and ask for The Young Adults Service Brain Tumour Support https://www.braintumoursupport.co.uk/ Samaritans (24/7UK wide) – 116 123 In an emergency, visit A&E or dial 999 Please don't be alone. We are here for you. Spotify, YouTube, Amazon Music, Apple Podcasts: @TheGlioBabes Instagram: @thegliobabes TikTok: @the.gliobabes LinkedIn: The GlioBabes Podcast *music by: SKIRK - soundcloud.com/skirkofficial Our guests share their personal experiences and opinions. We understand that everyone’s journey is unique, and what resonates with one person may not with another. We encourage open-mindedness and respect for diverse perspectives.

    35 min

  4. May 15

    S7. Ep. 5: Comparison Is The Thief Of Joy

    The GlioBabes, a podcast created by two young women who were both diagnosed with brain tumours at a young age. Mel and Mol are creating a safe space to talk about their experiences and to raise awareness of brain tumours and ill health within the young population. Welcome back for Season 7 Episode 5! Final episode of this season… “Comparison is the thief of joy” But it’s easier acknowledged than practiced. Especially if you’re watching everyone else around you move on… and you feel stuck. From navigating post life diagnosis, to grieving the 5 year plan we had, and redefining success after those personal milestones change, we cover it all! To the podcast episode we discussed, catch Dr. Alia Crum here: https://podcasts.apple.com/gb/podcast/1-mindset-expert-simple-mindset-shifts-that-transform/id1646101002?i=1000742032125 Laughter, tears, appreciation and hard truths… your promised intentional chaos is back. Link to the GlioGang fundraising page, added to Young Ambassador total: https://www.justgiving.com/team/thegliogang?utm_medium=TE&utm_source=CL Support links: The Brain Tumour Charity Call 0808 800 0004 Monday - Friday 9-5 Email support@thebraintumourcharity.org Young Adult team YAS@thebraintumourcharity.org Phone as above 0808 800 0004 and ask for The Young Adults Service Brain Tumour Support https://www.braintumoursupport.co.uk/ Samaritans (24/7UK wide) – 116 123 In an emergency, visit A&E or dial 999 Please don't be alone. We are here for you. Spotify, YouTube, Amazon Music, Apple Podcasts: @TheGlioBabes Instagram: @thegliobabes TikTok: @the.gliobabes LinkedIn: The GlioBabes Podcast *music by: SKIRK - soundcloud.com/skirkofficial Our guests share their personal experiences and opinions. We understand that everyone’s journey is unique, and what resonates with one person may not with another. We encourage open-mindedness and respect for diverse perspectives.

    32 min

  5. May 8

    S7. Ep. 4: We Asked, You Answered | Community Tips & Tricks

    The GlioBabes, a podcast created by two young women who were both diagnosed with brain tumours at a young age. Mel and Mol are creating a safe space to talk about their experiences and to raise awareness of brain tumours and ill health within the young population. Welcome back for Season 7 Episode 4! Today's theme of focus: advice by you guys, for you guys. In episode three, we asked you to send in your tips and tricks, words of wisdom and pieces of advice to other community members. From fatigue and epilepsy to mental health and financial support, we had advice come in from so many different angles. We couldn’t cover all of the answers in today’s episode, however they will be posted throughout the week on our social media channels. Thank you so much to everyone who sent them in. What a special episode! Support links: The Brain Tumour Charity Call 0808 800 0004 Monday - Friday 9-5 Email support@thebraintumourcharity.org Young Adult team YAS@thebraintumourcharity.org Phone as above 0808 800 0004 and ask for The Young Adults Service Brain Tumour Support https://www.braintumoursupport.co.uk/ Brainstrust brainstrust.org.uk Samaritans (24/7UK wide) – 116 123 In an emergency, visit A&E or dial 999 Please don't be alone. We are here for you. Spotify, YouTube, Amazon Music, Apple Podcasts: @TheGlioBabes Instagram: @thegliobabes TikTok: @the.gliobabes LinkedIn: The GlioBabes Podcast *music by: SKIRK - soundcloud.com/skirkofficial Our guests share their personal experiences and opinions. We understand that everyone’s journey is unique, and what resonates with one person may not with another. We encourage open-mindedness and respect for diverse perspectives.

    46 min

  6. May 1

    S7. Ep. 3: From Hospital Waiting Rooms to Scans: Our Hospital Hacks

    The GlioBabes, a podcast created by two young women who were both diagnosed with brain tumours at a young age. Mel and Mol are creating a safe space to talk about their experiences and to raise awareness of brain tumours and ill health within the young population. Welcome back for Season 7 Episode 3! Today’s theme of focus: the tips and tricks we’ve learnt along the way as patients. From navigating hospital experiences and appointments to preparing for scans and results, we talk all things fresh socks and lip balm… the stuff we would’ve loved to have know on day 1. We would love to do a part 2 to this episode of more general life outside the hospital… so please do send in your life hacks for living with a brain tumour! Laughter, tears, appreciation and hard truths… your promised intentional chaos is back. Link to the GlioGang fundraising page, added to Young Ambassador total: https://www.justgiving.com/team/thegliogang?utm_medium=TE&utm_source=CL Support links: The Brain Tumour Charity Call 0808 800 0004 Monday - Friday 9-5 Email support@thebraintumourcharity.org Young Adult team YAS@thebraintumourcharity.org Phone as above 0808 800 0004 and ask for The Young Adults Service Brain Tumour Support https://www.braintumoursupport.co.uk/ Samaritans (24/7UK wide) – 116 123 In an emergency, visit A&E or dial 999 Please don't be alone. We are here for you. Spotify, YouTube, Amazon Music, Apple Podcasts: @TheGlioBabes Instagram: @thegliobabes TikTok: @the.gliobabes LinkedIn: The GlioBabes Podcast *music by: SKIRK - soundcloud.com/skirkofficial Our guests share their personal experiences and opinions. We understand that everyone’s journey is unique, and what resonates with one person may not with another. We encourage open-mindedness and respect for diverse perspectives.

    26 min

  7. Apr 24

    S7. Ep. 2: The Brain Tumour Diagnosis Guide... With The Missing Pages

    The GlioBabes, a podcast created by two young women who were both diagnosed with brain tumours at a young age. Mel and Mol are creating a safe space to talk about their experiences and to raise awareness of brain tumours and ill health within the young population. Welcome back for Season 7 Episode 2! Today’s theme of focus: the real life happenings from a Brain Tumour diagnosis that the leaflets never cover. From the impact on identity in relationships to cognitive challenges and social anxiety, we cover the unspoken realities of living with a diagnosis and embracing the dark humour in adversity. But of course reflecting on the positive sides, from a shift in priorities and self care to celebrating our community and audience. There’s a lot to unpack this episode! Laughter, tears, appreciation and hard truths…your promised intentional chaos is back. Link to the GlioGang fundraising page, added to Young Ambassador total: https://www.justgiving.com/team/thegliogang?utm_medium=TE&utm_source=CL Support links: The Brain Tumour Charity Call 0808 800 0004 Monday - Friday 9-5 Email support@thebraintumourcharity.org Young Adult team YAS@thebraintumourcharity.org Phone as above 0808 800 0004 and ask for The Young Adults Service Brain Tumour Support https://www.braintumoursupport.co.uk/ Samaritans (24/7UK wide) – 116 123 In an emergency, visit A&E or dial 999 Please don't be alone. We are here for you. Spotify, YouTube, Amazon Music, Apple Podcasts: @TheGlioBabes Instagram: @thegliobabes TikTok: @the.gliobabes LinkedIn: The GlioBabes Podcast *music by: SKIRK - soundcloud.com/skirkofficial Our guests share their personal experiences and opinions. We understand that everyone’s journey is unique, and what resonates with one person may not with another. We encourage open-mindedness and respect for diverse perspectives.

    38 min

  8. Apr 17

    S7. Ep. 1: 1 in 3 | The Truth, The Reality, The GlioGang

    The GlioBabes, a podcast created by two young women who were both diagnosed with brain tumours at a young age. Mel and Mol are creating a safe space to talk about their experiences and to raise awareness of brain tumours and ill health within the young population. Welcome back for season 7! Mel and Mol together for the first time in a while, recapping on the professionals that joined for season 6, March's Brain Tumour Awareness Month happenings, from The Twilight Walk to Charity events, and how this week 2 years ago, was when The GlioBabes met for the first time. Today’s theme of focus: 1 in 2. 1 in 2. The terrifying cancer statistic we’re all hearing. 1 in 3 know someone with a brain tumour. A Rare Cancer. A Less Survivable Cancer. The biggest cancer killer of under 40s. It's all a lot. So we chat about it! This episode is understanding the 1 in 2 statistics, the need for innovation revisiting the emotional toll of awareness. Laughter, tears, appreciation and hard truths…your promised intentional chaos is back. Link to the GlioGang fundraising page, added to Young Ambassador total: https://www.justgiving.com/team/thegliogang?utm_medium=TE&utm_source=CL Support links: The Brain Tumour Charity Call 0808 800 0004 Monday - Friday 9-5 Email support@thebraintumourcharity.org Young Adult team YAS@thebraintumourcharity.org Phone as above 0808 800 0004 and ask for The Young Adults Service Brain Tumour Support https://www.braintumoursupport.co.uk/ Samaritans (24/7UK wide) – 116 123 In an emergency, visit A&E or dial 999 Please don't be alone. We are here for you. Spotify, YouTube, Amazon Music, Apple Podcasts: @TheGlioBabes Instagram: @thegliobabes TikTok: @the.gliobabes LinkedIn: The GlioBabes Podcast *music by: SKIRK - soundcloud.com/skirkofficial Photos credit of Imelda Turnock Our guests share their personal experiences and opinions. We understand that everyone's journey is unique, and what resonates with one person may not with another. We encourage open-mindedness and respect for diverse perspectives.

    36 min
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About

The GlioBabes Podcast. Real talk from young women living with brain tumours in their 20s. Unfiltered chats on health, identity, and life turned upside down, coming to you with dark humour and the raw unfiltered truth. Join Mel and Mol - and some special guests - weekly on your favourite podcast platforms.

Information

  • Creator
    Mel and Mol
  • Years Active
    2025 - 2026
  • Episodes
    44
  • Rating
    Explicit
  • Copyright
    © Mel and Mol
  • Show Website
    The GlioBabes

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