The actual outcome though is that I’m learning that I can bail on the idea that social interaction is something I should be performing in ways that don’t work for me. eg; if I can communicate without speaking, that is okay, actually. it is more comfortable for me and so long as I’m understood it doesn’t matter.

But yeah, I absolutely get to give up on trying to be normal or do things the normal way.

Also, “But you shouldn’t let it define you.” is literally the fucking worst for things that are integral to who I am. It is only ever used for things *other* people don’t want to think about or be aware of. How about I don’t let *you* define me, and then I can figure out who I actually am without the social bullshit.

All kinds of things are inescapable and define me, but I get to determine *how* they define me.

I’m not going to let someone else do it just because my definitions aren’t comfortable to “normal” people.

Sometimes I feel like autistic life is like living with a screaming child and you don’t know what it wants, but the child is you.

Today I’ve been feeling worse and worse and it got so intense I was trying a million different things and rushing around in a panic because I didn’t know what was bothering me and couldn’t cope. Then as soon as I tried my ANC headphones? The whole world was just “hi Sophie, welcome back.”

I’ve been trying to work on my self awareness so that I can tell when things are bothering me, and I’m definitely getting better at noticing there’s a problem before it gets out of hand…

But I still suck at telling just what the problem actually is unless it’s super obvious.

It’s like “great, for once I notice I’m freaking out. What the fuck am I supposed to do about that?” lol

Want to take a moment to talk about what I’m calling “pointless obstructive guilt” (which may have a name already, I don’t know) - it’s the tendency to feel guilty and locked up by things that are wrong in no way except for offending your arbitrary sense of balance. Like wanting to use your favourite cereal bowl but you don’t want the others to feel underused, or you start a puzzle with one method and see another will work better but you can’t abandon how you were doing it.

What I want to say about this is: wow that’s really annoying! Most of the time I can see it’s something that really doesn’t matter at all, I can do things in whatever way or whatever order and it will be fine.

But it won’t feel fine! And I’m torn between different options and feeling bad about it for no good reason. Who cares if I turn left a little more than I turn right in a day? Literally nobody is wronged, but I’ll feel bad anyway.

Another day when I find there is no greater cure than just taking a nap.

One of the best things about finally knowing I'm autistic is I can add "autism" to search terms that I've been stuck on for years and finally get a hit, like https://community.autism.org.uk/f/adults-on-the-autistic-spectrum/16550/i-can-feel-electricity-in-insulated-cables---or-even-someone-s-skin-if-they-are-holding-something-plugged-in

Clearly pretty rare and I don't think I'm *quite* as sensitive as this person, but it's definitely something I experience.

I can feel electricity in insulated cables - or even someone's skin if they are holding something plugged in - Autistic adults - Home - National Autistic Society - our Community

Last week I noticed that my webcam had little flickery lines it was picking up, but I had no idea where it was coming from. Later I felt an electrical vibration in my PC case even though it wasn't plugged in. With trial and error I found that the source was from a HDMI splitter into which the PC was connected and did have power. Turn off my TV and my PC doesn't feel electricy.

Like the linked post, iPads are definitely something I notice the most, the back of an iPad can feel completely different when it is plugged in vs when it isn't. Sometimes if it has to charge and I'm not comfortable with the sensation I have to just put it down until it is done.

Sensation is stronger with movement, like I'm feeling the bumps of an EM field or something.

Also it is a little variable, don't know if it is dissociation, variations in the power grid, or both.

(Obligatory "autism is not a super power" statement.

This has been a hinderance or a bother far more often than it has ever helped anything.)

Something really scary is the times I’m in distress but I’m not aware that it is happening, and not like an “I’m unconsciously experiencing bad things and not noticing” but the complete opposite “My existence is really bad and I’m upset but I don’t have the awareness to notice I have any agency and can mitigate it.”

I spent maybe an hour pacing and ticcing, really having a bad time, getting nothing done and looping through the same thoughts before out of nowhere “oh wait… everything will get a lot better if I just put on some noise cancelling headphones and take a painkiller.”

I was really upset but not *noticing* that I was upset, or that I have other modes, I was just a ball of existential suffering that had no mind to move out of that spot.

Anyway yeah scary because… maybe someday that will stick for more than just an hour or so, that will be my life. Complete misery with no way out because I’m incapable of processing my situation, and incapable of communicating the problems because I don’t see them, they are just me. Forever.

A frog in hot water with the heat always rising. It sucks but my experience and my agency have no relation. I stay put and suffer because I forgot how to know better.

I don’t know if I’m explaining it clearly, how about this:

Picture a nightmare where you’re panicked by something that seems trivial once you wake up. As soon as you’re awake you’re like “wow the solution was simple why couldn’t I do that when I was asleep?”

It’s like that. I just have sleep-logic running the show rather than my waking-logic.

I’m experiencing the situation but I’m not experiencing enough of my own consciousness to process the situation and take agency.

Today I was getting tired and stuck on a bug, I thought it would absolutely derail me but a headmate stepped in, wrote a bunch of code and said “that should do it” then switched out. I was like “wait wait wait, don’t go, you haven’t tested it and I don’t know what you changed!”

They were like “eh, trust me, it’ll work.” And it did. I think that is pretty cool tbh but also frustrating, why can’t I be that awesome?

I mean, “I” (collective) am… but “I” (singular)? Not so much.

I try not to dwell on it too much though, teamwork makes the dream work 💪
We just had our first serious fight as a system since realising we were plural. Discussing adaptations to help regulating overwhelm led to our memory keeper headmate voicing themself for the first time. It was really difficult because a bunch of expected norms for us had been established without them being truly conscious. They thought they were an exception (and to some degree maybe they are) so getting upset when they didn’t follow assumed norms spiralled really bad.

The irony of that post following the one before it in the thread is not lost on me :p

Anyway we’re okay now. It’s not like the issues the argument was about are solved, buuuuut we did manage to find ourselves a page that we can be on together.

I guess in hindsight it shouldn’t be surprising. There’s no real way for a traumagenic system to change/adapt/grow without potentially jostling some of that trauma. 🤷

Tempted to say something like “this thread will shortly go back to being mostly about autism and less about plurality” but then realised… nope it’s still my thread. I don’t need to hide any of the spice (though I also need to be okay with not sharing it also I suppose).

Anyway this thread will be whatever this thread will be.

Realising it is difficult to evaluate whether a pain is coming and going, or if it is always there and the headmates who tank it for me are coming and going.

The best I have is conducting a mental survey “should I take a painkiller” and if there is any “YES. ABSOLUTELY.” response, the pain is still there.

I think dissociation from pain is another one of those things that sounds like a superpower (and I’m not going to lie, I lean on it HEAVILY sometimes), but it really isn’t. You still take the damage it’s just harder to feel and heal.

Lately I’ve been thinking that I have no way to tell if I’ve been in pain for years. I got an unbearable toothache quite a while ago and then it just stopped. Has it never stopped and part of me has just been working overtime to separate us from it? It would explain some things, but I just don’t have any way of knowing.

Wish my brain had like a debug readout so I could check what is actually going on in there.

So here’s something I think I can finally articulate: noise-cancelling headphones cancel The Noise.

Okay yes that seems like I’m saying nothing, but The Noise is actually *incredibly* taxing, in a way that is hard to understand until it isn’t there.

Part of my head is working literally all the time, trying to manage all the input and it just doesn’t acclimate to all the din it should. Noise-cancelling gives me a break I never knew I needed.

Every time I turn it on I feel my thinking get clearer, easier. There’s less strain. It is quieter not just in my ears, but in my mind.

If you’ve never tried ANC headphones I strongly encourage it. If you’ve got a brain like mine the relief it gives is so worth it. In ways you might not know you need.

Okay this part of the thread might be squicky to some but I need to talk about it.

I just had a shower and as ever, it fucking sucked. It’s an immediate powerful sensory overload every time, unbearable without extreme dissociation (like, switching through several headmates to get though it levels of dissociation). And the stupid thing is, I’m going to not believe how bad it gets. In a few weeks I’ll think “nah, it can’t be that bad, and I’m feeling strong today.”

And then right away it’ll be “HOLY FUCK WHAT THE HELL FUCK FUCK FUCK.” and I’ll literally be in shock.

Normally my sensory memory is fucking aces, but I guess for some traumatic stuff not so much.

All I get is this vague sense of dread. I know it’s something I dislike but part of me is always thinking I avoid it because I’m lazy or I like to be gross. But I’m not, and I really don’t. I used to think it was dysphoria and wanting to not experience my body but-

-that’s not the issue either (apart from the aches, I’m pretty comfortable with my body finally!)

So now I’m left just knowing that dread I feel is a repressed sense of how miserable I have to make myself just to be clean. And yeah, it tends to take a few weeks before I do it again because I don’t like not being clean and “well, it can’t have been that bad” and I’ll have another miserable experience.

(I know there’s ways of coping. I take advantage of a bath whenever I can - but my flat doesn’t have one. Washing by a basin is *sometimes* okay but it comes with its own sensory challenges. For the most part I’m coping as best I can, but ultimately I have to accept that cleanliness has a huge cost for me.)
Thinking back, there was a health class or something at school, with a questionnaire that had the question “how often should you bathe” and how often I actually bathed wasn’t even an option so I picked the longest (like a week IIRC). When I saw people consistently answering 1-2 days I was so shocked. No idea how people could do it that often, I thought everyone must have been lying for a while.
Anyway, all of this is to say that we need to invent those sonic showers from Star Trek already. Just walk into a booth and all the grime falls away? Sign me up please.

Saw this today and it’s validating as hell. I frequently find myself arguing back and forth (with myself) “this didn’t used to be so bad, people saw us deal with it okay before” “No, people saw us dissociate so hard from our existence that the stresses became a diffuse haze to the point that everything sucked instead of having a few things suck a lot. It made those things a bit easier and everything else miserable.”

https://youtu.be/kVi5JoyKAJ8

Why are things more annoying in autistic self-discovery?

YouTube
It’s also reassuring to see that we’ve adopted some of the suggested changes just as a side-effect of embracing autism. When you know what your deal is it is a lot easier to find things that work for you rather than focusing on things that “should” work but don’t (which are absurdly frustrating).

Changing the CW to emoji because it’s cute.

Anyway today I’m thinking about how I don’t remember most of last week, but the sound of a friend falling down the stairs 30 years ago is echoing in my head with perfect clarity.

tbh this memory stings a lot because it’s the clearest memory I have of her rn and the reason she fell is the reason she isn’t around anymore. Epilepsy is a fucking monster.

Me: “Okay! I’ve got energy! I’ve got motivation! I’m going to do so much work today!”

My brain: “You’re going to yell random bullshit for 2-3 hours until you’re hoarse, then you’ll be unable to focus for another few hours. THEN you can work, IF I’m feeling generous.”

Something that bothers me the most about calling autism a “disorder” is that it implies a neurotype that is perfectly ordered.

Have you ever met a single person with a mind like that? They don’t exist at all (but if they did, I expect they’d be autistic).

This is exceptionally good https://youtu.be/x4ieMzbXiRA

Something I’m thinking about this morning is “non-verbal” vs “non-vocal”. It seems a lot of autistic folks prefer “non-vocal” because apparently “non-verbal” implies an inability to communicate at all… but I disagree.

When I can’t speak, I find vocal communication much easier! I like to think I’m pretty expressive and clear with simple voicing (“moan” type sounds of varying patterns and frequencies. Like, a “nuh-uh” is so simple and everyone understands it)

@Sophie this sounds like needing precision. vocal is about using voice. my patients (companion quadrupeds) are often vocal,never verbal. verbal is about using words. after my tonsillectomy I was verbal but non vocal.

I think sometimes the usage of non-verbal is non-vocal-verbal, which is social rather than strictly precise languages. I feel like your vocal non-verbal communication gets cut out in that model.