The Meningioma Cast

The one and only....D

Welcome to The Meningioma Cast — a podcast for brain tumor warriors, and anyone who’s ever had their life turned upside down by a diagnosis. I’m your host — a brain tumor survivor, cancer fighter, and someone who’s had to learn what it really means to rebuild from the inside out. This podcast is a raw, real, and honest journey through everything they don’t prepare you for after you hear the words, “You have a brain tumor.” This show is my way of making sense of that world — and hopefully offering a light for others walking a similar path. Support: https://www.patreon.com/c/MeningiomaCast

  1. 6d ago

    Who was I before my Brain Tumor? Life after brain surgery & losing your old self.

    Who were you before your brain tumor? And what happens when the person you used to be isn't quite the person you are today? A brain tumor doesn't just change your medical history. It can change your relationships, your career, your confidence, your priorities, and the way you see yourself. But here's something nobody really prepares you for: What happens when you survive brain surgery, but you're still trying to figure out who you are afterward? In Season 3, Episode 4 of The Meningiomacast, we're getting personal. I'm talking about life before my meningioma diagnosis, undergoing a craniotomy, and navigating the complicated reality of life after brain tumor surgery. We'll explore the emotional side of brain tumor recovery, changes in identity, the frustration of invisible struggles, and what it feels like when the world expects you to return to normal. We'll also talk about the things I've lost, the things I've gained, and whether getting back to the old me is even the goal anymore. And here's what makes The Meningiomacast different. This isn't your typical medical podcast. We're not sitting around reading clinical studies or pretending every day is an inspirational journey filled with rainbows and happy endings. This is real life. Real experiences. Real talk. Sometimes it's funny. Sometimes it's uncomfortable. Sometimes it's downright frustrating. And sometimes we're going to talk about things that people would rather sweep under the rug. We're talking about the realities of living with a meningioma, brain surgery recovery, mental health, personality changes, relationships, working after a craniotomy, and the emotional challenges of being a brain tumor survivor. No sugarcoating. No pretending we've got everything figured out. Just an honest conversation about surviving, adapting, and occasionally wondering what the hell happened to the life we had planned. Whether you're living with a meningioma, recovering from brain surgery, supporting someone with a brain tumor, or dealing with your own life-changing medical diagnosis, there's a place for you here. Because surviving is one thing. Figuring out how to live afterward is something else entirely. And you don't have to figure it all out alone. Have you experienced changes in your personality, identity, relationships, or outlook on life after a brain tumor diagnosis or craniotomy? Are you struggling to explain to others why you're not quite the same person you were before? I want to hear your story. 📧 Email: giomacast@gmail.com Share your experiences, ask questions, suggest future episode topics, or just reach out. This podcast isn't just about my journey. It's about connecting with people who understand what living through something like this actually means. And if you're new to The Meningiomacast, consider starting with Season 1, Episode 1 to hear how this whole journey began. Everyone has a story. This one is mine. #TheMeningiomacast #Meningioma #BrainTumor #BrainTumorSurvivor #BrainTumorAwareness #BrainSurgery #Craniotomy #LifeAfterBrainSurgery #BrainTumorRecovery #MeningiomaSurvivor #BrainTumorSupport #BrainTumorJourney #LifeAfterCraniotomy #InvisibleDisabilities #BrainInjuryRecovery #MentalHealthAwareness #SurvivorStories #PatientStories #LivingWithMeningioma #BrainTumorCommunity #LifeAfterDiagnosis #IdentityAfterIllness #RealTalk

    Who was I before my Brain Tumor? Life after brain surgery & losing your old self.
  2. Oct 7

    Working After a Craniotomy: Returning to Work With a Meningioma

    What is it really like to work with a meningioma, recover from brain surgery, and try to return to a normal work life after a craniotomy? In this episode of The Meningioma Cast, I talk about working while living with a meningioma, returning to work after brain tumor surgery, and the physical, mental, and emotional realities that can follow a craniotomy. We get into recovery, fatigue, concentration, confidence, neurological changes, stress, identity, and the strange experience of trying to function professionally while your brain and body are still adjusting. This episode is for anyone dealing with a meningioma diagnosis, brain tumor, craniotomy recovery, brain surgery recovery, returning to work after brain surgery, working with a brain tumor, neurological symptoms, or the long process of rebuilding life after surgery. I also talk about the things people do not always warn you about: the pressure to feel “normal,” the uncertainty around what you can handle, the fear of setbacks, the frustration of fatigue, and the challenge of balancing work, health, family, and recovery. If you are living with a meningioma, preparing for surgery, recovering from a craniotomy, returning to work, supporting someone with a brain tumor, or trying to understand what life after brain surgery can actually look like, this episode is for you. The Meningioma Cast is a podcast about meningioma diagnosis, brain tumors, craniotomy recovery, brain surgery, MRI scans, neurological symptoms, treatment, survivorship, work, family, mental health, recovery, disability, and life after a brain tumor. Real stories. Real recovery. Real life after meningioma. Everyone has a story. This one is mine. Contact the show: giomacast@gmail.com

    Working After a Craniotomy: Returning to Work With a Meningioma
  3. Sep 30

    Brain Tumor Battles

    Season 3, Episode 2: Brain Tumor Battles This week on The Meningioma Cast, I’m talking about some new developments in my health, including recent CT chest scans, new medical information, follow-up questions, and what happens when life decides one medical storyline apparently isn’t enough. But don’t worry. This episode is not 35 minutes of me staring dramatically out a rainy window. There’s been a lot of good since the last episode too. We’re talking about the weird balance of dealing with new health concerns while still living your life, finding things to laugh about, making plans, moving forward, and trying not to let every scan, appointment, and test result take over the entire damn story. If you’ve dealt with a meningioma, brain tumor diagnosis, surgery, follow-up scans, chronic health issues, medical anxiety, survivorship, or just the strange reality of trying to live normally while your medical chart keeps getting longer, I think you’ll relate to this one. And if you’re new to the podcast, go back and start with Season 1, Episode 1. The whole story makes a lot more sense from the beginning. Please leave a podcast review!!! Pretty please.--------- Giomacast@gmail.com As always... Everybody has a story. This one is mine. #MeningiomaCast #Meningioma #BrainTumor #BrainTumorAwareness #BrainTumorSurvivor #BrainTumorJourney #MeningiomaAwareness #MeningiomaSurvivor #BrainSurgery #HealthJourney #HealthUpdate #CTScan #MedicalJourney #Survivorship #LifeAfterBrainSurgery #PatientStory #PatientPerspective #ChronicIllness #MedicalPodcast #HealthPodcast #Podcast #PodcastCommunity #Season3 #BrainTumorBattles

    Brain Tumor Battles
  4. Sep 23

    "I'm Still Here"

    Season 3, Episode 1 Season 3 of The Meningioma Cast is officially here, and David has some catching up to do. In this episode, we dig into what’s been happening in the world of David: health, happiness, recovery, life after brain surgery, and the strange reality of living with a meningioma and everything that comes with it. Because here’s the thing about brain tumors: no two people experience them exactly the same way. Symptoms are different. Recovery is different. Fear is different. Humor is definitely different. Sometimes really different. I’m talking about you, Sharron. This isn’t a medical lecture and it definitely isn’t a motivational poster with a sunset behind it. It’s an honest conversation about brain tumor recovery, meningioma, neurological health, mental health, relationships, perspective, and figuring out what life looks like when your brain decides to rewrite part of the script. There are serious moments. There are ridiculous moments. There are probably things David should have kept to himself. So, basically, The Meningioma Cast is back. If you’re new to the show, go all the way back to Season 1, Episode 1 and start there. You’ll hear the original story, the diagnosis, the beginning of the journey, and everything that led us here. Whether you’re living with a meningioma, recovering from brain surgery, supporting someone with a brain tumor, navigating neurological health issues, or you just want to hear one guy attempt to make sense of an extremely weird chapter of life, you’re in the right place. Everyone has a story. This one is mine. EMAIL ME YOURS: giomacast@gmail.com #MeningiomaCast #Meningioma #BrainTumor #BrainTumorAwareness #BrainTumorRecovery #BrainSurgery #BrainSurgeryRecovery #MeningiomaAwareness #MeningiomaJourney #LifeAfterBrainSurgery #BrainHealth #NeurologicalHealth #PatientStory #Survivorship #HealthPodcast #MedicalPodcast #Podcast #PodcastSeason3 #BrainTumorCommunity #MeningiomaCommunity

    "I'm Still Here"

Ratings & Reviews

5
out of 5
6 Ratings

About

Welcome to The Meningioma Cast — a podcast for brain tumor warriors, and anyone who’s ever had their life turned upside down by a diagnosis. I’m your host — a brain tumor survivor, cancer fighter, and someone who’s had to learn what it really means to rebuild from the inside out. This podcast is a raw, real, and honest journey through everything they don’t prepare you for after you hear the words, “You have a brain tumor.” This show is my way of making sense of that world — and hopefully offering a light for others walking a similar path. Support: https://www.patreon.com/c/MeningiomaCast

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