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The Symptoms I Couldn't Explain

Writer: Lori Yvette
Lori Yvette
Jun 19
2 min read

I was fourteen when I first remember thinking, something doesn't feel right.

It started with headaches.

Not the occasional headache everyone gets, but headaches that became part of my normal life. The kind that made me keep ibuprofen nearby because I knew there was a good chance I'd need it before the day was over.

I'd be sitting in class when a familiar pressure would settle at the base of my skull. At the time, I didn't think much of it. I was fourteen. I assumed it would eventually go away.

But it didn't.

As time went on, other symptoms started showing up too.

Sometimes I would get dizzy for no obvious reason. I could be walking down a hallway, standing still talking to someone, or simply turning my head too quickly. For a moment, I'd see stars and wonder if that was normal.

Then I'd brush it off and keep going.

There was also something I now know as brain fog.

Back then, I didn't have a name for it. I just knew there were moments when thinking felt harder than it should. It was like my brain had to work overtime to process simple things. Sometimes it felt as though I was watching life happen instead of fully participating in it.

The hardest part wasn't necessarily the symptoms themselves.

It was not understanding them.

I didn't know what was happening to my body. I couldn't point to a cause. I couldn't explain why I felt different from everyone around me.

And when you're fourteen, that's a confusing place to be.

Everyone else seemed fine. They weren't dealing with constant headaches or random dizziness. At least not that I knew of. So I started wondering if maybe this was just normal and I was overthinking it.

So I did what a lot of teenagers do.

I kept going.

I went to school. I spent time with friends. I cheered. I smiled. I pushed through the headaches and ignored the dizziness whenever I could.

Life moved forward, and I tried my best to move forward with it.

Looking back now, I know those symptoms were the beginning of a much bigger story.

They weren't random. They weren't imagined. They were the first signs of a condition I wouldn't be diagnosed with until nearly a decade later.

A condition called Chiari Malformation.

But at fourteen, I didn't know any of that.

I was just a teenager trying to make sense of symptoms I didn't yet have the language to describe.

And if you've ever experienced unexplained symptoms yourself, you know how isolating that can feel.

Sometimes the hardest part isn't the pain.

Sometimes it's not having answers.


 
 
 

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