Neurodiversity & Parenting

🧠 Three Trips and a Lightbulb Moment


Last night, I needed my phone charger.

Simple enough, right?

Except I made three trips to the office before I ever got it.

  • Trip 1: I saw food left out in the kitchen. My brain latched on. “This needs to be handled.” So I handled it.
  • Trip 2: I heard Big Mac. He was still up—he hadn’t taken his meds. That became the new priority.
  • Trip 3: I finally got what I originally came for: my phone charger.

And somewhere between trips two and three, it hit me.

This is how my brain has always worked.


🧠 First Grade Was the First Clue

I was diagnosed with ADHD in first grade, in Mrs. Miles’ class.
But instead of support, I was pulled away from my classmates and placed at a separate desk.

They said it was to help me focus.
What it really did was label me, without a word.

No fidgets. No flexibility. Just isolation and pressure.
“Sit still. Focus. Try harder.”

That was the first time I remember feeling like I didn’t belong.

And the bullying? It followed fast and hard.


✨ The Exception

But not every classroom was a battlefield.

In 2nd and 4th grade, I had Mr. Lane.

He always met me where I was.
He didn’t shame me for how my brain worked—he adjusted.
He was calm. Creative. Patient.
He was my Mrs. Jones. The kind of teacher who stays with you long after the spelling tests are gone.

And it was in his class—the last week of 4th grade—that I finally started ADHD medication.

It didn’t fix everything, but it was the first time something lifted—the fog, the shame, the sense that I was just lazy.
For once, I could focus, and someone saw me instead of a problem.

In a blur of years where I was too much for most, Mr. Lane made me feel just right.


🪙 The Tokens

By fifth grade, in Ms. Arnold’s class, everything had gotten harder.
Puberty had started. My cycle had begun. Hormones were raging—and my ADHD symptoms intensified.

Her intentions weren’t unkind, but the system? It still missed the mark.

Their solution?

A manila envelope filled with three jagged squares of neon posterboard, cut hastily and uneven.

That was my limit:

  • Three times I could get out of my seat.
  • Three questions I could ask.

If I didn’t use them, I could save them.
Behavioral currency for basic needs.

This wasn’t support.
It was containment.

I didn’t need restrictions.
I needed understanding.
Instead, I got scraps of neon paper.


🔥 Fire #1 – The School

In fifth grade, I was outside playing when I heard the fire alarms blaring from the school.

We lived close enough that I could hear them from the yard—and when they didn’t stop, we went to see what was going on.

My school was on fire.

We later learned it was arson—someone had broken in with a blowtorch and set it.

Our class was displaced for the rest of the year.
We were first moved into the old multipurpose room, then into portables.
Nothing felt normal.
Nothing felt safe.

I had just started ADHD medication a few months earlier, at the end of 4th grade with Mr. Lane.

But it was hard to tell what was working when everything around me was on fire—figuratively and literally.


🔥 Fire #2 – A Flashback I’ll Never Forget

On my 13th birthdayJanuary 7th—I was in the last period of the school day when I heard the sirens:

Fire trucks. So many of them.

As I walked home, I saw the trucks lining the street.
I saw smoke rising above my neighborhood.

Then I turned the corner.

Our car was pushed up on a neighbor’s lawn—my mom had driven it there herself after seeing the smoke, rushing to reach the house and check on my brothers.

They had gotten home before me and followed our plan, running to the neighbors across the street.

And then I saw it:

Our building.
The two upper units were on fire.
Our ground-level home didn’t burn—but it was filled with smoke and flooded with water. Everything we owned was damaged.

We couldn’t stay.

We moved in with my grandparents.
I slept on a mattress in the formal dining room.

It wasn’t just what we lost.
It was how fast we had to leave it behind.


👀 Then My Son Looked at Me

Fast forward.

Big Mac— our son with autism—looked at me one day and said:

“Mama… maybe you’re like me.”

And I haven’t stopped thinking about it since.

Maybe it wasn’t just ADHD.
Maybe I’ve spent my whole life masking something more.

The sensory overload. The rigidity. The shutdowns.
The way I get so overstimulated I forget what I was doing in the first place.

Maybe it’s not forgetfulness.
Maybe it’s a lifetime of trying to act “normal” while quietly unraveling inside.

🦖 Don’t Step on a Crack

I saw the plan.

The desk chart. The new rules.
The quiet spaces that looked a lot like isolation in disguise.

And I saw my son—about to fall into the same cracks I had fought so hard to crawl out of.

Virtual learning didn’t feel safe.
It felt familiar.

“Don’t step on a crack, or you’ll fall and break your back.”
I used to think it was just a rhyme.
Now I know—it was a warning.


💬 What I Know Now

I may never have a paper diagnosis.
But I have a brain that keeps revealing more of its story every day.

I met with my therapist yesterday and told her about the blog.
I talked about what I’m starting to write, and the memories that won’t stop coming.

She told me what I’m doing is amazing.
She said this work is healing.

She’s encouraged me to journal my trauma before, but I’ve always said the same thing:

“I hate writing.”

I didn’t want to sit with it. I didn’t want to re-live it.

But this—this is different.

This is witnessing.
This is me giving voice to stories I’ve carried in silence for too long.

Stories I’ve only just begun to speak out loud.
Even Sparkey hasn’t heard them all.

Until now, I had only shared my pain story—and Small Fry’s birth.
But now they’re spilling out.

And I’m not trying to stop them.

Because I remember what it felt like to fall through the cracks.
And I’m building something steadier—for our boys, for our family… and maybe for me, too.

Health & Healing

When Sleep Is Mercy—and Progress Still Hurts

There are nights when I can’t find comfort in my own body. When every position feels wrong, and no amount of shifting or adjusting brings relief. My back feels like it’s being wrung out like a washcloth—tight, twisted, worn. Some spots burn sharp, like someone’s taken a knife and turned it slowly, just to see what gives. Other places just ache with a bone-deep fatigue that no amount of rest ever quite erases.

It’s hard to put into words, even for the people who love me most. But I try—because I need them to understand when I can’t keep pretending I’m fine.

Last night was one of those nights. I was so uncomfortable I couldn’t even settle. Just constant, restless pain. So we made the call: take the muscle relaxer. Not to fix anything, but to knock me out. Because sometimes the kindest thing I can do for myself is stop feeling—even if that means giving in to sleep I didn’t earn through peace, but through exhaustion.

It’s not weakness. It’s not giving up. It’s choosing mercy.

And today? I caught myself asking—why does everything hurt so bad? Where did I go wrong? I hadn’t overdone it. I hadn’t done anything wild or reckless.

But I had handled Harley on the leash at the shot clinic. I stood in line with other pets, kept him steady, kept me steady. That’s something I couldn’t have done even a month ago.

And sure, today I sat on a stepstool to move laundry from the washer to the dryer. But you know what? We adapted that space when we replaced the machines—not just so I could do it without hurting myself, but so I could do it without having to ask for help. We’re making our home work for me. That’s not defeat. That’s wisdom. That’s progress.

This body of mine—held together by faulty glue and a whole lot of grit—is getting stronger. The steps we’re taking are working. The strength is coming back. But healing has never meant painless. It just means I’m doing more in spite of the pain, and with a lot more wisdom along the way.

Rest isn’t weakness. Needing help doesn’t mean failure. And pain, as stubborn and sharp as it is, doesn’t get to steal the fact that I’m still going.

Even when it hurts.

Health & Healing

Ran Myself Over. Delivered a Baby. Still Kicking.

No, seriously — all of that happened.

People have been telling me for years:
“You should write a book.”
And maybe one day I will.
But if I’m honest? I think I hate writing.
What I do love is storytelling — the kind that’s messy, unbelievable, and holy in its own wild way.

I’m basically undefeated at Two Truths and a Lie, and not because I’m clever.
It’s because my truths sound fake, and my lies can’t keep up.

A Few Things That Still Stop the Room:

🚗 I hit myself with our own car.
Just once — but that was enough.
Harley, our sweet but chaotic Labrador, bolted, and I jumped out to chase him…
completely forgetting the car was still in reverse.
As I stepped out, the door slammed into my knee, knocking me flat.
The car crept across the road into the neighbor’s driveway.
Harley? Climbed into the driver’s seat like he owned it.
Me? I got back up — with a broken knee — and climbed back in to secure the car and check on our boys.

👶 I delivered a baby by accident.
Not mine.
Just me and a neighbor in crisis. No warning. No time.
By the grace of God — and extremely outdated EMT training from two decades ago — I caught that baby steady.
Also: probably way too much TLC, Call the Midwife, and “this might come in handy one day” medical TV.
Turns out, it actually did.

🛒 I ran my foot over with a cart of banquet tables.
Deeply on-brand.

🏍️ I ran over my own ankle with an ATV.
Because I thought speed = height.
I went flying. The ATV kept going and ran me over for good measure.

🏥 My GP sent me to the ER for a kidney stone.
That’s when they discovered it had retrograded — gone back into my kidney.
My urologist blinked and said, “I’ve heard of that. Never seen it.”
Welcome to life with Ehlers-Danlos Syndrome.

🫃 During my hysterectomy, they found my uterus fused to my bladder.
That surgery became a medical write-up.
Because my body doesn’t follow the rules — it writes new ones.


It’s Ehlers-Danlos Awareness Month.
And y’all, this is what EDS looks like.

  • Dislocations.
  • Fatigue.
  • “Mystery” symptoms for years.
  • Being told you’re dramatic or anxious.
  • Hearing “I don’t know how to help you anymore” from your doctor.

I was 39 when I was finally diagnosed.
Thirty-nine years of being undiagnosed — and misjudged.

I was told to lose weight, that it would help my pain.
So I lost 111 pounds — and the pain? Got worse.
Because the problem wasn’t my size.
It was the glue in my body — that genetic connective tissue — breaking down quietly, constantly.

EDS isn’t fixed by a diet.
It needs truth, treatment, and tenderness.


Now?
I’m fighting for proactive care for our son — Small Fry — who shows all the early signs.
And this mama isn’t waiting 20 more years for someone to believe him.


Why I Tell These Stories:

Because someone out there thinks they’re too weird or too broken to be believed.
So let me say it plain:

✨ You are not too much.
✨ You are not alone.
✨ You are not forgotten.

The grace of God has saved me more than once.
Patrick and I together? That’s a miracle in itself.
(His birth story’s coming soon — buckle up.)

Maybe that’s why I love memoirs.
Because real life — even the hard, wild, ridiculous kind — makes the best kind of story.

No book (yet).
Just battle stories.
And a faith that’s still standing — even on a broken knee.


Welcome to the Things You Can’t Make Up series.
Where the chaos is holy, the strength is earned, and the grace runs deep.

You belong here.
Especially this month.
Especially if you’re a zebra too.