The Meningioma Cast

What happens when you look perfectly fine on the outside, but you're fighting a battle nobody can see?

In this episode of The MeningiomaCast, David gets personal about the hidden realities of living with a brain tumor, surviving brain surgery, and navigating life with an invisible illness.

From neurological challenges, balance issues, and chronic fatigue to the emotional exhaustion of constantly telling people "I'm fine," David explores what it really means to live with a condition that doesn't always show itself to the outside world.

We talk about the pressure to appear healthy, the frustration of being misunderstood, the impact on relationships and family, and why asking for help can sometimes be harder than facing the illness itself.

David also opens up about the future of The MeningiomaCast, the challenges of keeping an independent podcast alive, and how listeners can help this growing community continue reaching people affected by brain tumors.

Because looking okay and being okay are two very different things.

If you're living with a meningioma, recovering from brain tumor surgery, dealing with a chronic illness, or supporting someone who is, this episode is for you.

Help keep The MeningiomaCast going!

Subscribe, follow, rate, and share the podcast. If you or your organization would like to help support, sponsor, or promote the show, we'd love to hear from you. Every share helps another person feel a little less alone.

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Everybody's got a story to tell. This one's mine.

#TheMeningiomaCast #Meningioma #BrainTumor #BrainTumorAwareness #BrainTumorSurvivor #InvisibleIllness #InvisibleDisability #ChronicIllness #BrainSurgery #BrainTumorRecovery #NeurologicalDisorders #BrainHealth #MentalHealthAwareness #ChronicFatigue #LifeAfterBrainSurgery #PatientAdvocacy #PatientStories #BrainTumorSupport #YouLookFine #LivingWithABrainTumor

What If It's Cancer? The Reality of Scanxiety

Brain tumor anxiety doesn't end when the surgery is over. Sometimes the hardest part is waiting for the next scan.

In Season 3, Episode 5 of The Meningioma Cast, host David shares the emotional reality of living with a brain tumor diagnosis, facing another MRI, and confronting the terrifying question: What if it's cancer?

From scanxiety and the fear of a cancer diagnosis to the emotional roller coaster of follow-up imaging, uncertain test results, and life after brain surgery, this episode explores what happens when your health refuses to give you peace of mind.

Whether you're living with a meningioma, recovering from a craniotomy, navigating a brain tumor diagnosis, or supporting someone through their medical journey, you're not alone.

The Meningioma Cast is a personal, unfiltered podcast about brain tumors, recovery, medical uncertainty, mental health, and finding humor and hope when life gets complicated.

Have a brain tumor story to share? We'd love to hear from you. Send your questions, experiences, or ideas for future episodes to:

Email: [email protected]

Listen, follow, and share The Meningioma Cast on Spotify, Apple Podcasts, and YouTube Podcasts. Give me a review and vote up!

Everyone has a story. This one is mine.

#BrainTumor #Scanxiety #Meningioma #BrainTumorAwareness #BrainSurgery #MRIAnxiety #BrainTumorSurvivor #TheMeningiomaCast

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: [email protected]

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

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: [email protected]

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.<---------

[email protected]

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

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: [email protected]

#MeningiomaCast #Meningioma #BrainTumor #BrainTumorAwareness #BrainTumorRecovery #BrainSurgery #BrainSurgeryRecovery #MeningiomaAwareness #MeningiomaJourney #LifeAfterBrainSurgery #BrainHealth #NeurologicalHealth #PatientStory #Survivorship #HealthPodcast #MedicalPodcast #Podcast #PodcastSeason3 #BrainTumorCommunity #MeningiomaCommunity

Welcome back to The Meningioma Cast. This one’s a real-life check-in. I talk about where things are at with my health, what it’s like getting around with the new cane, and how I’m keeping my head straight when things get frustrating.

If you’re dealing with a brain tumor, meningioma recovery, chronic pain, or just one of those stretches where life feels heavier than it should, this episode is for you. No sugarcoating, just what it actually looks like to keep going and stay positive when it’s not easy.

We get into recovery, mindset, and figuring out how to move forward when your body doesn’t always cooperate.

If you’ve been there, you’ll get it.

Reach out anytime: [email protected]
Cane I’m using (Not a paid sponsor): Asterom.com

In Episode 10 of The Meningioma Cast, I’m talking about the everyday reality of life after a brain tumor, and some of the things nobody really prepares you for. We get into the long list of medications many of us end up taking after meningioma surgery, the strange journey of recovery, and the gear that sometimes becomes part of the process… including my walking boot and even canes.

This episode is part catch-up, part real talk about chronic pain, recovery after brain surgery, and learning to adapt when life throws you a neurological curveball. If you’re a brain tumor survivor, dealing with meningioma, recovering from brain surgery, or supporting someone who is, this conversation will probably sound familiar.

How many meds are you taking these days? I’d love to hear from you.

Email the show: [email protected]

The Meningioma Cast is a podcast about brain tumors, life after meningioma, chronic illness, recovery, mental health, disability, and finding humor in the middle of a very strange journey.

Everyone has a story. This one is mine.

[email protected]

It’s been a minute, so this episode is a catch-up and a reset. I’m talking honestly about my health, life after a meningioma, and what The Meningioma Cast is really about. This is a brain tumor podcast, a survivor story, and a real talk show about recovery, chronic pain, mental health, and the weird reality of living after brain surgery. It’s not for kids and it’s not sugar-coated. It’s for emotionally mature adults who can handle some cursing, some dark humor, and some honesty about medical trauma, scans, and learning how to live with a new normal. No hype. No miracle cures. Just the truth from my side of the scar. Everyone has a story. This one is mine.

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Sorry I got it wrong on the show...I have drain bamage, what can I say!!!

Search "The Meningioma Cast" on Google, Facebook, and wherever your brain tumor leads you... Thanks friends.

meningioma, brain tumor, brain surgery recovery, cancer podcast, chronic illness, disability, survivor story, mental health, medical trauma, health podcast, patient story, recovery journey, dark humor, real talk, MRI anxiety, caregiver support, life after surgery, chronic pain, invisible illness

Season 2 Episode 8

This week I’m talking neurologist visits, epilepsy medications, and the ongoing surgery aftermath that no one prepares you for. It’s a peek into the bureaucratic side of brain tumor recovery, the trial-and-error of meds, and the quiet reality of living with a disability that isn’t always visible.

If you’re navigating seizures, specialists, appointments, or the post-op rollercoaster yourself, you’re not alone. This episode offers the honest play-by-play — with the usual dark humor and refusal to sugarcoat — because real life after a brain tumor doesn’t fit the inspirational quote format.

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