09/10/2026
Autistic Inertia ramblings - if you think you've been experiencing ADHD paralysis, this one might also be for you.
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"My kid has been getting so 'stuck' and sometimes we can ask them if they want us to move them and they say yes,
and sometimes they say no.
Should we be presuming they are 'stuck' more often and ask about moving them more? Especially when they're engaged with electronic devices, we're worried they would appreciate us moving them if they are 'stuck' and unable to tell us they would want that."
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How much have you looked into autistic catatonia?
I'm part of a research group that's working on autistic inertia, and one theory we seem to be circulating in consensus on is the idea that
autistic inertia may occur when we are burnt out from our
communicative,
processing,
social, and
sensory needs
going unmet for too long...
And that there appears to be different degrees to which we will have these experiences.
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We seem to agree that autistic inertia is the mental difficulty of movements, but that we still have some control over some of our limbs, if not all....
While autistic catatonia appears to take this and dial it up to 10, making it
nearly impossible for any of our limbs to move.
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I experienced my own autistic catatonia for the first time a few weeks ago, and it was so incredibly scary;
I wanted to move, needed to move, but as soon as I started consciously phrasing the thought of what I could do TO get my body moving,
my body immediately locked up AND my brain froze;
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I would compare the experience to when I have been running a computer too hot for too long,
but it's still somewhat capable of running in the sense that I have
too many programs open, but
one of those programs is frozen while I
can still technically access other programs with the mouse, but the instant
I tried to click on the frozen program or move my mouse across it, the mouse itself stutters and I worry about it freezing too.
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When the lock up occurred, I happened to have my phone in my hands with my thumb still able to move.
I happened to be open to the messages from my partner, who was in the room next to me.
It felt like if I tried to turn my neck towards them, my neck was going to snap, so I didn't.
Instead I moved my thumbs to type messages to them, trying to make it as urgent as possible:
"sos help can't move stuck sos ambulance? Can't move"
But I couldn't get their attention.
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I had to just sit there and wait, hoping that something in my behavior would give off weird vibes.
They did notice after a minute or two, and that helped me feel a little bit more shocked into trying to be present, though I still couldn't move.
I experience terrible body and vestibular migraines as a result of languaging and auditorily processing too much,
so I have celebrex I take for in-the-moment migraines that can only be taken x amount of days per month.
I honestly wasn't sure what was going to help, but I figured taking something would be better than taking nothing.
"Celebrex x1"
They grabbed my medication and tried to hand me the bottle and water. I couldn't make myself grab it. I panicked; how was I supposed to get this medication that might help me into my mouth?
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I was desperate, so I texted "pill in hand move towards my mouth."
As they picked up my hand and started to move it,
I started to panic again at the thought of my hand finally reaching my mouth and me not being able to open it to take the pill or swallow.
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I do think it was this level of panic, combined with the
help of my partner in reverse engineering my motor processes that
allowed me to force my mouth open and to take the water and quickly swallow.
I felt freed; I could move!
It still felt rough, and hard, like a squeaky and stuff robot needing to be oiled, but I didn't want to undergo that again so I mentally beat myself up into moving.
I texted my partner again to get into a comfortable position where I could lay in their arms and put on a comfort show.
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My medication takes about half an hour to kick in, so whether it was in fact neurologically helpful even though I may or may not have been experiencing a migraine,
or whether it was feeling disrupted through
muscle memory of movement thanks to my partner,
or perhaps the feeling of the comfort show that allowed me to
disengage from panic...
Most likely the combination of all of them.
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So what can I recommend for your child?
Definitely keep up your consent-based approaches!
As I continue to do research into autistic inertia / catatonia, the more I wonder about whether
this is our body's way of protecting us from trying to do too much, particularly in the concept of processing.
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I constantly feel like my software is running a million miles a minute (AuDHD), like I'm
constantly processing way too much information, and always, the world is either
moving too slow for the speed my brain needs, or
moving too fast.
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I feel like I've spent so much of my life trying to comply with assimilation,
trying to think differently about my own existence, and now I just can't keep doing it anymore;
it hurts my brain to process in that way.
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This is what I mean by "language too much" as well;
I didn't realize that for decades I had been trying to translate the way I naturally think into English language or other verbal language, and then communicated that out loud...
because people wouldn't understand my natural language if I communicated in my natural way.
Based on my nonverbal and non-speaking history as a child,
I strongly suspect now that it would be a mixture of gestalt sounds, and body movements.
It's why sign language, especially in ASL form over SEE or PSE,
feel so much more natural and accessible to me;
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As a person who was forced into verbal language, I've learned to think about the world differently...
And ASL has been letting me get back in touch with naturally thinking in a way that makes me feel comfortable;
Through pure observation and reaction, without analyzing it deeply.
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I have felt an enormous amount of relief in this process, in
trusting that my subconscious mindsets that influence my decision-making processes
are authentic to the person I want to be,
and allowing my instinctive reactions to be led by that guide.
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Mind you, I am still very early in this process that I don't think I've heard other people describe.
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I think that it is a very rare occurrence for someone to be
"as disabled as I am"
and to also have been so high masking for so long that I
"benefited from verbal education"
such that I can analyze my own state of being (thanks to my autism and the last 7 years of childhood trauma, betrayal trauma, and societal-neurodivergent trauma healing)
and properly understand my neurodivergence.
Don't get me wrong, there are MAAAANY autistics out here who can accurately claim the same about their experiences;
where my experiences may make my case a unique study is that I have both
experienced AND can articulate about:
+ neurological migraines
+ ASL & Deaf culture
+ dyspraxia
+ extreme APD from AuDHD
+ childhood & ABA trauma
+ betrayal trauma
+ societal-neurodivergent trauma
...that I have the experiences of EVERY "level" of autism and ADHD and still have the faculties to communicate about them.
for now.
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I've been experiencing what looks like a steady decline into more permanent non-speaking,
and occasionally I worry about whether they could process into nonverbalism altogether.
That would then make these statements about my experiences potentially my last.
Eh.
I certainly hope not, and
instead choose to see this as,
"I am becoming the autistic I was always meant to be, and
I am finally giving myself permission to
just exist
the way I always deserved as a human being to exist."