When Your Body Feels Everything: Autism, ADHD, and the Pain No One Sees

This post was hard to write because it’s hard to explain—but I need to try.

A person walking on a sidewalk, wearing a gray sweatshirt, gray shorts, and sneakers, with a smile on their face. In the background, there are trees, a power line, and a residential area.

People often ask if I’m okay.

Usually, the answer is no—but not in the way they think. I’m not sick, not injured, not recovering from surgery or fighting off a cold. My body just… hurts. All the time. Not in a dramatic or even easily explainable way. Just in this persistent, buzzing, exhausting way that lives in my shoulders, my jaw, my stomach, my spine.

And no, it’s not “just anxiety.”
(Though sure, anxiety shows up too. It’s got VIP access at this point.)

What I’m trying to say is: I’m autistic. I have ADHD. And I carry pain—literal, physical pain—in my body almost every single day. It builds up in places I can’t always stretch out or rest away. I hold tension in my neck like I’m bracing for a crash that never happens. I clench my jaw until it aches. My back is a battlefield. And don’t even get me started on my digestive system.

But here’s the thing:
I didn’t get into a car accident. I didn’t pull something.
I didn’t do anything to deserve this pain.
I just am—sensitive.

Too Much, All the Time

Autistic and ADHD bodies often feel like they’re tuned to a different frequency. The world that others experience as background noise can feel like a full-blown rock concert in my nervous system.

Loud sounds? Tension.
Bright lights? Tension.
An unexpected comment, a small conflict, a passive-aggressive email? Yep, tension.

Even when something good happens—something exciting or beautiful—my body reacts. Because emotion, for me, is physical. Joy floods my chest. Grief sinks into my hips. Shame slithers into my stomach. I don’t just think or feel emotions—I store them. I wear them.

And that would be fine if my body were some kind of emotional Tupperware container. But it’s not. It leaks. It overflows. It breaks down.

My 20s Were a Blur of Pain

Through most of my 20s, I had terrible, unexplained pain—especially in my neck, shoulders, and traps. No injury, no diagnosis. Just a kind of constant body-scream no one else could hear.

Every time I brought it up to a doctor, they seemed confused. My nurse practitioner once offered me muscle relaxers, but I declined. I was already managing enough meds—ADHD, depression, anxiety—and didn’t want to add another layer.

I tried getting massages. They felt great in the moment, but the pain always came back. Same with chiropractors. I saw a couple, even committed to a full treatment plan. Each time, they’d say something like, “Have you been in a car accident recently?”
Nope. Never.

They couldn’t understand how my neck could carry that much stored trauma unless something had physically happened to me. But something had happened—just not in the way they expected. I’ve been living in a body that reacts to the world like it’s too much, too fast, too loud. Because for me, it is.

Yoga, stretching, and meditation help. They really do. But the relief is temporary, because the world doesn’t pause. The moment I reenter it—back into the bright lights, clashing sounds, sudden emotions, and social expectations—the pain starts crawling back in.

My ex-husband used to give me back massages, trying to help. He’d say it felt like bubble wrap back there—except not the kind you can pop. Just these crunchy, stuck little knots of tension. That’s what I carried. Still do.

Hypersensitivity Isn’t a Metaphor—It’s Neurological

There’s research out there that explains this better than I can. Studies show that autistic individuals often have increased sensitivity to pain, altered pain thresholds, and heightened interoception—meaning we feel internal sensations (like heartbeat, muscle tension, or digestive discomfort) more intensely.¹ ADHD adds its own chaos: constant scanning, restlessness, hyperawareness, and the never-ending effort to regulate.

And then there’s emotional pain, which doesn’t stay in my mind—it lives in my body. Especially when I’ve masked all day, ignored my own needs, or absorbed the feelings of everyone around me like a walking sponge.

When It’s Invisible, It’s Dismissed

This is what people don’t see when they ask if I’m okay.
They don’t see the full-body effort it takes to not fidget or cry or shut down in public. They don’t see the internal screaming when a light flickers or someone interrupts me four times in a row. They don’t see the pain that comes from trying to seem “normal.”

Because it’s not just the sensory overload—it’s the masking. It’s the people-pleasing. It’s the emotional labor of trying to be less “too much.”

I’m not saying all autistic or ADHD people experience pain like this—but I am saying many of us do. And I’m one of them.

So If You’re Reading This…

Maybe you’re one of those people who never understood why I cancel plans last-minute. Or why I seem so tired all the time. Or why I talk like I’m on fire, but move like I’m underwater. Maybe you’ve never realized how much pain a body can hold when the world keeps pushing too hard, too fast, too loud.

Or maybe you do know what I mean. Maybe your body hurts too, for reasons no one else sees or believes.

To you, I say: you’re not imagining it.
And you’re not alone.

We are bodies that feel too much in a world that demands we feel nothing. But our pain is real. And it matters.

A graphic summarizing the relationship between neurodivergence and chronic pain, highlighting how autistic individuals experience altered pain sensitivity and ADHD can increase physical tension and restlessness.

🧠 Research & Footnotes

  1. Autistic People and Pain Perception
    • Research shows altered pain thresholds and heightened pain responses in autistic individuals. Some report being more sensitive to certain types of pain, while others may under-report it due to interoception difficulties or alexithymia.
    • Source: Failla, M. D., et al. (2020). “Pain Perception in Autism Spectrum Disorder: A Review.” Journal of Autism and Developmental Disorders.
  2. ADHD and Somatic Complaints
    • Individuals with ADHD are more likely to report chronic pain, headaches, and somatic symptoms, likely tied to nervous system dysregulation.
    • Source: Mikita, N., et al. (2015). “Somatic symptoms and their association with anxiety and depression in children and adolescents with ADHD.” European Child & Adolescent Psychiatry.
  3. Interoception and Emotional Pain
    • Neurodivergent individuals often experience interoception differently, which can lead to heightened awareness of internal pain and discomfort, and difficulty identifying or verbalizing these sensations.
    • Source: Quattrocki, E., & Friston, K. (2014). “Autism, oxytocin and interoception.” Neuroscience & Biobehavioral Reviews.

💭 Unmasking: The Struggle of Being Myself

Unmasking, One Post at a Time

I’ve been doing a lot of thinking lately. Specifically about unmasking my autism. And while I’ve had some positive experiences with it, I’ve come to realize that the negative experiences still outweigh the positive ones. And that makes me really sad. It’s hard, honestly, because I don’t know what else to do or who else to be. I can’t be anything but myself, and sometimes it feels like that’s just too much for people to handle.

I know I’ve gotten some positive responses—people have been understanding, kind, and validating—but still, the negativity lingers. And that’s tough. It’s like a heavy weight in my chest. When my mom was sharing her experiences with unmasking, I couldn’t really respond in the way I wanted to. I wasn’t sure how to say it, but I’ve been feeling like my own experience of unmasking has been harder.

A person sitting on a bathroom toilet, holding a small white dog and a bundle of flowers, with a smile on their face. The bathroom features green walls and a vanity with toiletries in the background.

For me, it’s not just about letting go of the mask. It’s about trying to explain the way I move through the world. I feel like I need to explain why I do certain things, like singing loudly to myself or having the song “Jingle Bells” stuck in my head 24/7. Or why I sometimes talk out loud to myself, the animals, or even inanimate objects around me. These are stims. If you don’t know what stimming is, I suggest you look it up. It’s a way of self-regulating, a form of expression. It’s something that helps me feel grounded. But it’s also something that makes me feel like I have to explain myself to others.

A person smiling while posing next to vibrant green leaves and clusters of white flowers in a natural setting.
Mmmmmm smells so good.

Here’s the thing: I can talk to animals or inanimate objects with ease, but when it comes to talking to people? That’s when I freeze. That’s when it gets too weird. It’s like my brain can’t quite make the connection, and then the pressure of social expectations just hits me. So, I just keep it inside. I don’t feel free to express myself the way I want to. And that’s painful—not just mentally, but physically too. Holding in stims isn’t just hard emotionally; it hurts in my body, and it’s depressing. It’s exhausting to try to be something I’m not.

A close-up view of a flowering strawberry plant with a white bloom and green leaves emerging from dark soil in a pot.

I’ve spent so much of my life masking my true self because I thought it would make things easier. But it hasn’t. Not really. And now, as I’m unmasking, I’m faced with all these conflicting feelings. The sadness of wanting to be myself, but also feeling like I have to explain why I am the way I am. It’s like trying to explain the air I breathe or the way my heart beats. It’s me. It’s who I am. It’s autism. It’s ADHD. It’s my brain. It’s my body. Take it or leave it.

A smiling person holding a dandelion flower in a backyard with cloudy skies and a white fence in the background.

But sometimes, when I’m still caught in the moments of doubt, I wonder: what would it be like to just be free? Free from the expectations, the need for explanations, the weight of others’ judgment. It feels so far out of reach some days. But I hold on to the hope that one day, the world will be a little more understanding and a lot less demanding of conformity.

Smiling person in a yellow jacket sitting by a riverbank, with a laptop in front, surrounded by lush greenery and a cloudy sky.

So yeah, I’m unmasking. And it’s a process. A painful, raw, beautiful process. And I’m doing it for me.

A close-up selfie of a person with long hair, wearing a bright yellow jacket and a colorful striped sweater, standing outdoors with a wooden structure in the background under a cloudy sky.

Title: Hyperfocused on Gardening: A Neurodivergent Spin on a Joyful Day of Planting

A black cat sitting inside a gardening planter on a patio, with additional empty pots nearby.

Today was one of those days where everything just clicked, and I got completely lost in something. I mean, I was hyperfocused—like, buzzing with excitement. My whole body was practically tingling with joy as I worked my way through this gardening project. If you’ve ever felt so into something that your entire body is just lit up, you’ll know exactly what I mean.

A person potting new plants on a wooden deck, with a black cat nearby. The individual is wearing a red floral top and white shorts, holding a gardening tool. A container for planting is visible in the foreground.
Me & Frodo during the potting process (which I’ll have to redo, but that’s OK!)

For a while now, I’ve wanted to grow a garden—not just flowers in pots, but something I could eat. Something I could snack on, something healthy. My first thought was strawberries. I’d love to grow them and just pop them in my mouth right from the garden. But, as it turns out, they were a little too expensive for my budget today (they were $30, which is way out of my price range). I’ll definitely be getting them eventually, but today wasn’t the day for strawberries.

Person taking a selfie in a mirror wearing a white shirt with paint splatters and a visor, sticking out their tongue and showing a playful expression.

As I walked through the garden center, I started thinking about what I could grow within my budget. That’s when I spotted cucumber plants, and it was like a lightbulb went off in my head. Cucumbers! They’re perfect for snacking, and I could totally make pickles someday. And at $4.56, they were a great fit for my budget. So, I grabbed one.

Then I saw it. Lavender. Oh, lavender. It was $5.37, and I had to have it. I debated for a second but knew I couldn’t leave without it. I was about to stop there, but THEN, when the cashier rang me up, I found out both the cucumber and lavender were on sale for $3.33 each. I couldn’t resist—so I ran back and grabbed a cantaloupe plant I had also been eyeing. It was my third choice, but at that price, it was totally meant to be!

A person sitting on a patio with potted plants, a black cat nearby, and a dog lying on the grass in a backyard setting.
HEY! 😀

I was so stoked, I couldn’t wait to get home and start planting. Now, I’m not a pro, but I had enough of an idea of what I was doing. I potted the plants into the containers I had on hand, but here’s the thing—after a little more research, I realized that I’ll definitely need bigger pots. So, that fun repotting session? That’s coming either tonight or tomorrow. I’m looking forward to it, though, because I’m excited to give them the space they need to grow.

Overgrown catnip plant and soil in a backyard with a white fence in the background.
A rustic wooden planter box sitting on grass, with a plain background.

And, of course, I also found out that cucumbers and cantaloupe need trellises, which sent me into another hyperfocused spin. I started Googling how to make trellises, and then I was texting my dad about any random pieces of wood he has in his garage (he has a ton, believe me). The idea of building my own trellis has me pretty hyped, and I can’t wait to see how that turns out.

The other part of my day that really lit me up was working with my hands to clear out the overgrown catnip plant in the backyard. I grabbed my cutters, started pulling out weeds, and getting all dirty in the soil was just so satisfying. I didn’t realize how much I’d enjoy using a hoe until today. It kind of felt like swinging a softball bat, but in a really productive way. So, I got a little workout in too (no complaints there). My muscles are definitely feeling it, and I think I’ll be sore tomorrow, but it was totally worth it.

By the end of the day, I had cucumber, cantaloupe, and lavender plants sitting in their new pots (for now). The backyard looks a million times better with the catnip cleared out. And honestly? It was so much fun. I was so into it that I forgot time even existed. This whole gardening thing? It’s turned into one of my “special interests,” and I think it’s a perfect example of how my neurodivergent mind works. When something captures my attention, it grabs hold of me fully. And today, gardening was that thing.

If you’re wondering what “special interests” are, they’re basically things that autistic people get really into. It’s not just a passing fascination, either. Special interests can bring so much joy and motivation. For me, gardening (and my house plants) has become a major part of that. It’s one of those things that makes me feel energized and alive in a way that’s hard to describe unless you’ve experienced it yourself.

Anyway, today was a reminder that it’s okay to get lost in something that excites you, even if you don’t have everything figured out. Sometimes, it’s about the joy of doing something right then and there, just because. And hey, if you haven’t tried gardening yet, I highly recommend it. It’s grounding, it’s thrilling, and it’s incredibly satisfying.

Thanks for reading! Drop a comment if you’ve had any hyperfocused moments (or gardening wins). I’d love to hear about it!

🧠 Unmasking, One Moment at a Time

Part of the “Unmasking, One Post at a Time” series

Content Note:
This post explores masking, self-awareness, and the quiet moments of learning to be real. If you’re currently in a hard place with identity or self-acceptance, please take care while reading.


I used to think unmasking would be one big, dramatic moment.

Like a grand reveal. A breaking point. A phoenix rising.
And sometimes, it is.

But most days?
It’s much quieter than that.

It’s not wearing makeup when I don’t want to.
It’s asking, “Can you say that more directly?” instead of pretending I understood.
It’s sitting how I actually want to sit, even if it looks “weird.”
It’s saying no to a hangout, not because I’m busy—but because I don’t want to go.
It’s admitting I need more time, or quiet, or clarity.
It’s not faking a laugh when I didn’t get the joke.
It’s pausing.
It’s stimming.
It’s choosing softness instead of performance.


I still mask.

Let’s be clear—I still do it.
Because this world isn’t always safe for neurodivergent folks.
Because unmasking doesn’t mean suddenly being “free”—
It means slowly, carefully learning which parts of yourself deserve protection and which ones are finally safe to let out.

The mask slips off in layers.

Sometimes it clings.
Sometimes I peel it off only to reach for it again five minutes later.
But other times—I forget I even had it on.

And those are the best moments.


📝 Poem: I Didn’t Mean to Wear It

I didn’t mean to wear it—
the smile, the nod, the soft yes
when my body said no.
It’s stitched into me sometimes,
automatic,
like muscle memory.

But today—
I caught it halfway on.
I paused.
And let the silence speak
instead of the mask.

That’s a win.
That’s a whisper of healing.
That’s me.


🪞 A Memory

A few days ago, I was at the grocery store and someone I vaguely knew from high school waved.
She asked how I was.
And I almost did it.
The default: “Great!” with a grin, head tilt, eyes wide.

But instead, I shrugged a little.
“Honestly? Been better. But I’m okay.”
And just like that, the interaction felt human. Not scripted.
She smiled back—genuinely.
We didn’t force a conversation.
We just… existed next to each other for a moment.
And that felt good. Real.


This week, I noticed I didn’t fake a smile in a conversation where I used to.

I didn’t force small talk.
I didn’t interrupt myself with apologies.
I caught myself, and I let myself stay real.
Not perfect. Just real.

And that’s enough for now.


🌀 Reflection Questions:

  • What does unmasking look like for you right now?
  • Can you remember a moment this week where you were fully yourself, even just for a second?
  • What would it feel like to unmask just 5% more in one part of your day?

Tags:
#Unmasking #NeurodivergentLife #AutismAcceptance #BeingReal #SelfDiscovery #MentalHealth #MaskingAndUnmasking #EverydayCourage

None of Your Business: Bodily Autonomy and the Power of Being a Woman

Salt-N-Pepa were yelling truth through my headphones when this essay started writing itself in my head.

“If I wanna take a guy home with me tonight, it’s none of your business!”

I wasn’t just listening—I was lip-syncing, stomping around my home like a woman possessed. That song doesn’t ask for permission. It doesn’t play nice. It kicks down the door and makes space for a woman to say, I belong to no one but me.

And as I sang those words loud enough for the neighbors to hear, I realized: this is it. This is the whole damn point.

Women get practically nothing in this world—not full safety, not full respect, not equal rights. But if we don’t even get our own bodies? Then what do we have left?

I’m not totally hopeless. I wish I could say I believe the patriarchy will collapse in my lifetime, but I don’t know. Maybe it will—and if it does, I’ll probably cry and pee myself out of pure joy. But until then, I want to be crystal clear about one thing:

A woman’s body belongs to her. No one else.

Let me say it louder:
I’m a grown-ass woman, and what I do with my body is none of your fucking business.


Objectified at Birth

From the moment we’re born, people start telling us who we are based on how we look.

“She’s so pretty.”
“Look at those eyelashes!”
“You’ve got a little heartbreaker on your hands!”

Compliments before we can walk, before we can speak—and they’re always about our appearance. Pretty. Cute. Beautiful.

Have you ever heard someone walk up to a baby boy and say, “He’s so handsome, he’s gonna break hearts”? Not really. Boys are strong. Boys are tough. Boys are smart. Girls are pretty.

And so it begins—this quiet but constant training that tells us our worth lives on the outside. That we are here to be looked at. That our bodies are not just our own, but for others to comment on, rate, touch, control.

By the time we’re old enough to notice, it’s everywhere.
Dress codes. Street harassment. Politicians making choices about our reproductive rights.
Our bodies have been claimed by everyone but us.

And that is terrifying. That is infuriating.


Silenced in Real Life

It’s not just politics. It’s not just headlines. It’s in my friend groups. Especially with my guy friends.

I try to speak—talked over.
Try to share—told to shut the fuck up.
Try to exist—mocked, ignored, laughed at.

And when I yell—because sometimes that’s the only way to be heard—I’m called dramatic. Crazy. “Too much.”

What am I even doing there, then? What’s the point of friendship if I’m just background noise?

I try to explain patriarchy. I try to talk about gender and fairness and equity. But I’m treated like I’m making it all up. Like I’m the problem. Like I’m speaking a language they’ve already decided not to understand.

It’s isolating.
It’s exhausting.
It’s one of the reasons I’ve wanted to die.

Not the only reason—but a big one. Because when the world constantly erases you, it’s hard to feel like you matter. Like you belong.

And then there’s the confusion. Am I here to be pretty or respected? Do I have to choose?

Add autism to the mix—undiagnosed until 32—and people still act like they know me better than I know myself. “You don’t seem autistic.” “Are you sure?” Yes. I’m fucking sure. I’ve spent years untangling this. I’m still learning. We all are. But people don’t even try.

And still—here I am.
Saying it out loud anyway.


The Power They Can’t Take

For everything this world tries to strip from us—our voices, our safety, our sanity—it still hasn’t found a way to take the one thing that lives deep in our bones: our power.

It’s not the kind of power written into law.
It’s older than that.
Wilder. Quieter. Unshakeable.

And I wouldn’t trade it for anything.

If reincarnation is real, I’d come back as a woman again. Every time.

Because even though this world tries to make it seem like being a woman is a disadvantage, there’s something we carry that can’t be touched. A generational fire. A knowing. A legacy.

I think of all the women who weren’t allowed to speak. Who weren’t allowed to choose. Who weren’t allowed to dream—and still, somehow, they survived.

They fought. They wrote. They whispered truths. They lit the path. And now I’m here—pissed off, alive, and writing this.

Sometimes I think about Buffy the Vampire Slayer, and it all clicks. She holds the power of every girl before her. She fights because they fought. That’s what womanhood is to me.

Yes, I’m tired.
Yes, I’m angry.
But I am not alone.


Hope That’s Bigger Than Us

I don’t know if I’ll live to see the day women have full autonomy.
But I hope someone does.

I hope some girl grows up in a world where her voice is not just tolerated, but expected.
Where she doesn’t have to choose between being pretty and being respected.
Where her body is hers and hers alone.

Where no one tells her she’s “too much” for daring to take up space.

Where she’s free to be loud.
To be weird.
To be whole.

That world may feel far away.
But hope is power, too.

Sometimes it’s just the decision to keep going.
To write. To scream. To speak anyway.

Because even if they don’t listen—
We’re still here.

And I’ll keep blasting Salt-N-Pepa, stomping through my house, saying it as loud as I need to:

“It’s none of your business.”

My body. My rules. My life.

Try and take that from me—and see how loud I can be.