Living With Brain Mets Is Like Sharing Your Head With a Stranger

There are days I wake up and don’t recognize my own thoughts.

Not because I forgot who I am—but because the way my brain reacts to the world feels unfamiliar. Louder. Faster. Sharper. Sometimes slower. Sometimes foggy. Sometimes angry in a way I never used to be.

Living with brain metastases is like sharing your head with a stranger who doesn’t ask permission before touching things.

They move your emotions around. They change how pain shows up. They turn minor stress into panic and quiet moments into something heavy and loud. I can feel myself overreacting and still not be able to stop it. I can hear the words coming out of my mouth and not recognize the tone they’re wrapped in.

That part is terrifying.

No one prepares you for the way brain mets mess with your sense of self. Doctors talk about size, location, treatment plans. They don’t warn you that your patience might disappear. That your memory might betray you mid-sentence. That you might feel like you’re watching yourself from the outside, wondering when you’ll get control back.

Some days, I don’t trust my own thoughts.

Is this fear real—or is it swelling?

Is this sadness mine—or chemical?

Is this anger justified—or neurological?

There’s a constant second-guessing that comes with having a sick brain. A quiet shame that creeps in when your reactions don’t match who you know you are.

And then there’s the expectation to still be “normal.”

To still be kind.

Still be patient.

Still be understanding.

Still be grateful.

But my brain is fighting battles my body can’t show you. Migraines that feel like pressure from the inside out. Fatigue that doesn’t respond to rest. Emotional shifts that hit without warning. And the fear—always the fear—that this is just the beginning of another loss.

I grieve the version of me who trusted her mind.

The woman who didn’t have to analyze every emotion for medical meaning. Who could feel without questioning whether her brain was lying to her. Who didn’t need grace for simply existing.

Living with brain mets means learning how to live with uncertainty inside your own head. It means apologizing for things you can’t fully control. It means asking the people who love you to see past your reactions and trust your heart instead.

Some days, I do okay.

Some days, I feel like I’m sharing space with something that doesn’t belong to me—and I’m just trying to coexist.

If you’re living with brain mets too and this feels familiar, please know this: you are not broken. You are not “too much.” You are navigating something unimaginably complex with a brain that is doing its best under impossible circumstances.

And that counts as strength—even when it doesn’t feel like it.

A note to my readers

If this post found you because you’re scared, newly diagnosed, or quietly Googling symptoms at 2 a.m., I want you to know you’re not alone here. This space exists for moments exactly like that. The Resources page was built to help you find information, support, and grounding when everything feels overwhelming.

If you’re able and would like to help keep Mojo and the Mess going—for me, for my care, and for others who find this space when they’re drowning—you can do so in a few ways:

💗 Support through PayPal

https://www.paypal.com/donate/?business=NR39Y7BVRBKRU&no_recurring=0&item_name=Help+keep+Mojo+and+the+Mess+going+💗+Every+donation+supports+my+story,+my+care,+and+this+blog.+Thank+you!+🐾&currency_code=USD

🐾 Amazon Wishlist (comfort items + daily essentials):

https://www.amazon.com/registries/gl/guest-view/10QFFEWQ9YHD8

If this blog has helped you feel seen—even once—please consider subscribing. Subscriptions aren’t just numbers. They’re how this space keeps existing, keeps reaching people, and keeps telling the truth when it’s hardest.

Thank you for reading. Thank you for staying. Thank you for being part of this community.

🐾

Mojo would say: I don’t know what’s happening inside her head. I just know it’s my job to stay close.

P.S. If you don’t have the energy to comment or share, subscribing is the quietest way to support this space. No pressure—just gratitude. 💗

One response to “Living With Brain Mets Is Like Sharing Your Head With a Stranger”

  1. mshibdonssciencelab Avatar

    Take whatever time you need to find some peace and calm. You have so much coming at you in all directions. I am here for you always. I love you so much. Your words are so honest. Keep being you. Hugs!

    Like

Leave a comment

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.

Let’s connect