Nicole Filippone, Autistic Advocate & Author
@sensorystories.bsky.social
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Advocating through science based education, validation, and empathy Nicolefilipponeauthor.com/my-links
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sensorystories.bsky.social
If you recently discovered you might be autistic or you're a parent who recently discovered your kiddo might be autistic & you're looking to learn about autism through science and lived experience...

Hi... I'm Nicole! 👋🏻
sensorystories.bsky.social
But that's what I mean by internalized meltdowns.

When your brain and body are hijacked for survival. You're in distress. You need help. But no one sees any of it.

I sincerely hope this explanation helps. ❤️
sensorystories.bsky.social
At home, when the stakes are less urgent and the people around me love me and have room for my humanity, my distress does show up at times... but the truth is... now that I know what I need and have learned to simply ask for it... that is a rare occurrence these days.
sensorystories.bsky.social
Which means that outwardly, especially in high-stakes contexts (like work) people would have absolutely no clue I was experiencing any distress at all. I look completely calm (even though I am frantic on the inside).
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I can't think. I can't breathe. I am basically mentally incapacitated. I start to hyperventilate, and I become frantic.

But... for me, this all happens internally. Because I have learned to internalize and hide my distress for social safety and survival.
sensorystories.bsky.social
So, if the trigger is there, I am instantly dysregulated and if I can't remove the trigger VERY quickly, that dysregulation turns into distress in a matter of minutes... sometimes seconds.

When this happens, my brain and body get completely hijacked...
sensorystories.bsky.social
Here's an example of what I mean. I'll stick with the simplest one for this post... sensory triggers.

There's nothing I can do to make my brain not react to sensory triggers.

And in most cases, they are extreme and intolerable from the outset. I don't have "mild" sensory triggers.
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In other words, we do not and cannot control how our brains react to our triggers.

Which, again, are tied to unmet needs. HUMAN needs. (See my previous post on what autistic needs are for a lengthy explanation on this.)
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A person MIGHT have the ability to mask how that reaction looks to others (by internalizing it)... but the internal experience (regardless of how it looks to others) is completely INvoluntary.
sensorystories.bsky.social
Meltdowns are also involuntary. It's the brain and body's automatic reaction to extreme triggers (even if those triggers seem "mild" to everyone else).
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Which brings me to my next point...

Outward (visible) meltdowns are a cry for help. Not a manipulation tactic.

They come from a place of DESPERATION, not manipulation.
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Meltdowns are tied to unmet needs.

Not wants. NEEDS.

And they happen when those needs go unmet for long enough that our initial dysregulation becomes much more urgent and turns into full blown distress.
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So, internalizing our distress becomes a matter of survival and we internalize our meltdowns.

I'll talk about the internal experience of these types of meltdowns in just a minute, but first I want to make a few things very clear...
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This happens when we (autistic people, often high masking) learn to internalize our distress so others don't see it...

Because having visible meltdowns in most contexts comes with severe social consequences. Which makes visible meltdowns unsafe for us.
sensorystories.bsky.social
Internalized autistic meltdowns, let's talk about them.

First of all, they can and absolutely do often look like they sound.

But they can also look like absolutely nothing.
sensorystories.bsky.social
Internalized autistic meltdowns. Anyone interested in a post on this?
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What makes autism a disability is that we (autistic people) need support to get our human needs met.

And that our needs go unmet more quickly and more frequently than the average nonautistic person.

I hope this helps. 🙂
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Which impacts us in significant ways and often impedes our ability to do important life activities without support.

Hence why autism is considered a disability.

BUT autistic needs... human needs... are not what make autism a disability.
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So our dysregulation shows up more quickly and more frequently than it does for nonautistic people.
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And based on everything I know about autism through psychology, neuroscience, and lived experience, I think the only difference between us and everyone else is that we have different thresholds of tolerance for when our needs go unmet.
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So people are made to think our coping behaviors ARE our autism when really, they're just how our autism MANIFESTS when our needs go unmet.

This is why I believe all autistic behaviors (especially the ones they put into the diagnostic criteria) are manifestations of unmet human needs.
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And what happens next?

What we do to regulate ourselves (whatever behaviors we demonstrate to self soothe or cope) becomes what they see and call autism... which then goes into diagnostic manuals like the DSM.
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Because our behaviors seem mismatched to the situation.

Why? Because no one around us has reached their tolerance threshold yet.

So they think we're overreacting when they see us dysregulated and distressed.
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All humans experience sensory overload if there's enough sensory overstimulation.

But autistic people reach their threshold of tolerance way sooner than the average nonautistic person.

And this stands out when it happens to autistic people for a very specific reason...
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We don't have different needs from the rest of the world.

What we do have is different tolerance levels and thresholds for when our needs go unmet (this is backed by both psychology and neuroscience).

The simplest example of this is sensory overload...
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So what exactly are autistic needs?

This is probably the most confusing aspect of autism.

I think the reason this confuses so many people (even autistic people) is that autistic needs are literally just human needs.