When they said it was in my brain, I swear the floor disappeared beneath me.

I already knew what it meant for cancer to spread. I knew the vocabulary—“metastatic,” “progression,” “treatment options.” Words that sound clinical to everyone else but rip through you when they’re aimed at your body.

But hearing “brain mets” was different. It wasn’t just another organ on a scan. It wasn’t my liver, my lungs, or my bones. It was me. My thoughts. My words. My memories. My personality. The part of me that makes me who I am. Suddenly, I wasn’t just fighting for time anymore—I was fighting for myself.

A Whole New World of Doctors

Brain mets come with a whole new cast of characters: neurologists, neurosurgeons, radiation oncologists, specialists with long titles and unreadable expressions. Each appointment feels like a revolving door of strangers asking me to hand over pieces of myself.

I sit in waiting rooms clutching my phone, wondering how I’ll explain it all later. Wondering how many bills will come from this one conversation. Wondering if this doctor will see me as a person or just as another case file.

Cancer is already expensive before it decides to crawl into your brain. But once it does, the cost multiplies—financially, physically, emotionally. Another copay. Another denied claim. Another afternoon spent waiting for insurance to decide if my life is “worth” covering.

The Things No One Prepares You For

They don’t tell you how loud the world will feel when your brain is involved.

They don’t warn you about the way sounds can crash against your skull, or how you’ll lose words mid-sentence and stare at a loved one’s face, panicked, because the thought is there but stuck.

They don’t prepare you for the dizziness, for how standing up can feel like stepping onto quicksand.

They don’t talk about the constant shadow of wondering if today will be the day you seize.

And they definitely don’t talk about the guilt. The guilt of knowing how much your care costs, how much your family sacrifices, how much debt piles up just for the chance to keep you here a little longer.

When “Fighting” Feels Like Losing

Lately, my mets are popping up everywhere. I’m not getting better. The scans keep showing more. And now there’s this choice hanging over me like a storm cloud: brain radiation.

I don’t want to do it. I don’t want to sign up for more pain, more side effects, more days lost to treatments that can’t promise me anything but exhaustion.

Everyone says “keep fighting,” but what does that even mean when every treatment feels like giving away another piece of yourself? When it’s no longer about curing but about enduring?

I’m tired of enduring. I’m tired of hospitals, of losing hair, of vomiting in parking lots, of forgetting my own words, of living in this cycle of scan, treat, decline, repeat.

This is the part no one talks about—the quiet, agonizing moment when you start to wonder if doing “everything” is still worth it.

The System Is Cruel

The reality is that brain mets don’t just attack your body. The system that’s supposed to save you does too.

“Payment due.”

“Insurance pending.”

“Denied.”

I can’t tell you how many hours of my life I’ve lost to waiting on hold, to explaining over and over to some insurance rep what “metastasis” even means, to fighting for treatments I didn’t ask for but can’t survive without.

It feels like I’m not just battling cancer. I’m battling paperwork, portals, and policies designed to exhaust me until I give up.

No Roadmap

There’s no manual for this. No guidebook that tells you how to grieve the version of yourself you might lose while still showing up for scan after scan, consult after consult.

There are days I feel like I’m drowning in it all—the doctors, the bills, the endless appointments.

There are days I’m furious.

Days I sob until I can’t breathe.

Days I go numb because the weight is too heavy to carry.

And yet, here I am, still here. Even with all of it.

To Anyone Else Living This

If you’ve heard “brain mets” and felt that sickening drop in your stomach, I want you to know this: you’re not alone in the chaos.

Even when it feels unbearable, even when the system is cruel, even when you’re tired of treatments and wondering how much more you can take—you are still here. And that matters.

Your existence is not measured in appointments or bills or scan results. It’s measured in you. And no metastasis can take that away completely.

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4 responses to “The Weight No One Prepares You For”

  1. penguinwise8f60778b5f Avatar
    penguinwise8f60778b5f

    Your words are difficult to read, Izzy… No one outside of your family can truly understand the battle you fight. Im in awe how you find the strength and courage yet you do. You are inspiring to many, please, never lose sight of that fact. God Bless 🙏

    Liked by 1 person

    1. izzypwbmma Avatar

      Thank you for always reading and supporting. It means the world.

      Liked by 1 person

      1. penguinwise8f60778b5f Avatar
        penguinwise8f60778b5f

        You’re very welcome, Izzy. I’m thankful you share your words for all to see. Your struggle is real… You’re gracious to share.

        Like

  2. alwayselectronic06c81330f4 Avatar
    alwayselectronic06c81330f4

    My beautiful girl. I wish I could do more. Always here though. I’m so sorry Sent from my iPhone

    Like

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I’m Izzy

Welcome to mojo and the mess, This isn’t the blog I ever expected to write — but it’s the one I needed.

I’m Izzy, a twenty-something living (and dying) with terminal cancer, navigating the messy, heartbreaking, unexpectedly beautiful in-between. Here, you’ll find raw reflections, real talk, dog snuggles (shoutout to Mojo), and the unfiltered truth about what it’s like to face the end of your life before it really got going.

This space is for the ones who’ve felt forgotten, the ones who don’t know what to say, and the ones who are still holding on. It’s not always pretty, but it’s always honest.

Thanks for being here. You’re part of the mess now — and I mean that in the best way.

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