I love the episode Virtual Systems Analysis.
A) it’s a representation of an autistic person (I’m just gonna go ahead and call Abed autistic) with imagination! The idea that autistic people can’t imagine things irritates me so bad. In my experience, though I don’t know how prevalent, autistics often have a ridiculous amount of imagination.
B) The high pitched squeal Abed makes when he’s on the verge of meltdown / when something has been changed that fucks with his brain. I was like, OMG I DO THAT TOO!
C) When he says “there’s a lot of things I can’t do” in the voiceover near the end and you see his head surrounded by four images. I’m not sure what the papers are, but the others - tying shoelaces, reading analogue clocks, and calculating tips or splitting up meal payments - all of those are things I have a really hard time with too.
D) Aughdghdkfhs the locker scene. Helloooo my childhood. “It’s a place where people like me get put when everyone’s finally fed up with us.” And the running scenarios for all possible situations.
Maybe it’s filling out forms, the papers? I know that’s something I can’t do and actually need one on one support for to get through.
Important Anouncement:
Autistics, allies, disability advocates, and disability activists, State Representative Sanchez of Massachusetts has expressed approval of the Judge Rotenberg Center. He has brushed off attempts to question his support of the torture of children on American soil. We are invading his Facebook page tonight. Please participate. People with our labels are suffering on his watch. Innocent kids are shocked until their skin burns. He thinks this is a good idea. Show up. Be civil. Do not make threats. Post your own sentiments or links. Post late at night into the early morning hours. We want him to wake up to this. We want people to see it before his staff can take it down. Please signal boost this message. I hope to see you there.
Listen to the Largest Minority Radio Show on WBAI for April 25th, 2012 CAPTIONED
I had a friend break the audio down into 4 parts, and I put it to a background so that it could be in video format. Then, I captioned them all!
I’m interviewed in parts 2 and 3. It was pretty awesome. we talked a bit about representation and stuff, and in part 3 about the vigils, and particularly about the part of the vigils I was involved with- the virtual vigil. :)
Also, huge skill building here, As I called in and talked on the phone live. BIG DEAL YOU GUYS. I have phone anxiety to the point where I don’t do conference calls without having someone willing to relay what I type for me on the call. I get scared to call for pizza or a cab. But! I’ve decided that the skill I’m working on this year is those around my phone anxiety and doing this show is a big part of how I’m working on building those skills. Yes, that’s right, self-directed life-skills building- hard work, scary, but still self-directed and thus less of a chance to have it be coercive or abusive. /OT
part 4… erm. Well. It’s a mother being interviewed in the last part, and there is sadly some fail including promoting an Autism $peaks walk. But! the rest of the show was awesome, and on the bright side even if some of her content was fail, it’s great to see more working class Latina voices? I just hope that Her son ends up growing up awesome and adding his voice to our community… even if his mom just doesn’t get how f-cked up A$ is.
But otherwise, yes. CAPTIONED! Whoooo!
Autism rights/neurodiversity is the radical notion that autistics are people.
p-3a:
I always feel like I can’t stim unless I’m alone. Even though I know I should be fine with doing it and that hey maybe a few of the “you must be very high-functioning!” lot would take mine and the doctors’ words for it a little more. But for some reason I can only bring myself to do socially acceptable stims (leg-jiggling is a big one, repeated hand-washing if I’m doing badly) unless I’m completely alone.
Rocking is nice. Yes.
A lot of people have a hard time with this because they were trained so hard core. It can be scary to reclaim yourself after that sort of training.
Good news! My college’s autism program wants me to help start a chapter for The Autistic Self Advocacy Network!
congrats!
(Source: tmkristen)
Listen up, allistics. You don’t want to listen to us - the autistic people? You only listen to organizations supported by celebrities (ahem Autism $peaks ahem)? Fine. Here’s a video for you with celebrities talking about how autism should be talked about.
Someone showed me this video about a year or so ago. I got so freaking excited that there were people talking about autism in this way. I’m still brought to tears every time I see this video, because I think, hey, maybe everyone doesn’t want me to be nonexistent. Maybe I do have a place in this world somewhere. They have a Facebook page that I visit often.
EEEEE the video my voice is in is making the rounds again! I’m the savannah BTW!
The month of April: Autism AND Child Abuse. I wrote about both.
Trigger warnings: physical, emotional, sexual abuse.
It’s long.
Brace yourself…the autism fear-mongering is coming.
Become a Member of the Autistic Self Advocacy Network
I would love to see you all become members if possible! (and if you have extra cash, maybe sponsoring a membership for those without?)
Declaración Conjunta de ASAN y Sociedad de Autismo sobre DSM-5
(The Joint statement from ASAN and the Autism Society, in Spanish/en espanol)
Tired.
I’m tired of being misrepresented. I’m tired of seeing the principles of self-advocacy misrepresented. And I’m tired of seeing the autism rights movement misrepresented.
Let me be clear. I’m not talking about allies, or about people who were just thrust into Autismland and don’t yet know much, if anything, about the constant conflicts that erupt here. This isn’t about you.This is about people who write things like John Elder Robison’s “Looking forward at the autism spectrum,” or Mark L. Olson’s “Autism’s Fly-Over Population,” or the comments on Susan Senator’s “The Parents Vs. The Autistics.” It’s been a week of frustrating, misleading, and outright hurtful writing.And I’m tired.
Non-speaking, “low-functioning”- by Amy Sequenzia
I am autistic, non-speaking. I am also labeled “low-functioning”. This label is a pre-judgment based on what I cannot do. It makes people look at me with pity instead of trying to get to know me, listen to my ideas.
I am a self-advocate and I can type my thoughts. But, at the moment I show up with my communication device and an aide, my credibility, in the eyes of most neurotypical people, is diminished.
My world of random, incessant thoughts :): Can anyone explain this to me, and tell me if I am completely off the...
Can anyone explain this to me, and tell me if I am completely off the mark please?
Theres a little boy at my older childs preschool centre with really severe autism. He doesnt verbally communicate with anyone, and has very little interactions with people at all. In fact, he generally tries to…
Yes.
There is a connection.
I have an entire binder somewhere full of descriptions of such interactions between autistic people. Some of those descriptions are written by autistic people ourselves, others by people observing us. But such descriptions truly are everywhere if you know where to look.
There’s a lot of reasons you won’t hear about this a lot from “experts”. Here are possibly the top three:
1. It contradicts established theories about autism. Such theories are that autistic people are autistic because of some kind of “social skills area of the brain” that isn’t working and therefore will never work even among each other.
(Note: Plenty of scientific evidence contradicts this theory. Morton Gernsbacher is a researcher and mother of an autistic boy who has taken such ideas apart very well. If you Google her, her website has papers on it. And I’ve personally seen her son absolutely blossom around similar sorts of autistic people.)
2. A lot of the time, nonautistic people miss social signals sent by autistic people. Both because their expectations tell them there are no such signals (and expectation colors what people perceive), and because some of our signals are hard to pick up on if you don’t know exactly where to look. So our communication often goes on right under people’s noses and they can’t see it for one reason or another.
3. Because this happens most often among autistic people with certain commonalities between each other. So you can’t just stick two random autistic people in a room and expect it to happen.
An important note about that last one — the groups of autistic people with common traits, are almost never the same as the official diagnostic groupings. So it also doesn’t work to stick two people diagnosed with the same type or severity labels in a room together and expect communication.
Like personally I’m diagnosed with autism. Usually nobody uses functioning levels on me, but when they do they usually say something along the lines of “severe”. At this point in my life. (Long story. Assume absolutely nothing and you’ll be better off.) The person most similar to me in the world is an engineer who is diagnosed with variously PDDNOS or AS (of the two PDDNOS fits better due to speech issues). Most people looking at her see competence and most people looking at me see incompetence. But people who know us both well have asked if we were separated at birth because we are that similar. Other people I find easy to communicate with include people with every severity label, every diagnostic label, every level of spoken or written language. Other people I find impossible to communicate with span the same range.
People like to say autism is about communication, social skills, and repetitive behavior. I prefer to say (and much research seems to agree) that it’s about sensory perception, thinking, and movement. All the social/communication/behavior stuff is someone else’s perception of an outward manifestation of the sensory/cognitive/movement stuff. In my observation, autistic people who “click” with each other have some degree of similarity in sensory perception, thinking, and movement even if their behavior looks radically different to a nonautistic person.
There are also lots of different degrees of clicking. My friend Anne and I can communicate without even trying. My friend Laura and I read each other reasonably well but have major, major differences. I’ve met autistic people who are harder for me to understand and communicate with than nonautistic people. (My brother is one of them, unfortunately. Just trying gives me a headache.)
Also one thing I’ve noticed is that it’s not just our abilities when at our best that determine these things. In many ways it’s our abilities at our worst. Or at least our abilities when at a normal comfort level. For me, I can write language very well at my best and understand language decently. However my baseline is no receptive language and minimal if any expressive language. That means that anyone who can only communicate by language will give me migraines trying to keep up with and anyone who expects lots of language will wear me out. Also, it matters how language is used. I unfortunately can’t describe that. It’s very subtle but important.
In my sort of default state, the world is a lot of swirling sensory patterns with no ideas on top of them. I can sense and deal with those patterns very well. When I am around someone enough like me, there’s no requirement of language at all, we may not even appear to others to be interacting, but in subtle ways how we interact with our environment we are very much aware of each other. Other times we may interact more directly.
It’s often easy for me to see when someone will make sense to me. It’s like I have different depths of awareness of different people. Some I will see very minimal threads I can piece together, other people pop out fully three-dimensional and everything obvious. And many stages in between.
I remember shocking a group of researchers and family members by pointing out that they had to stop talking and help an autistic man fix his schedule because he was looking more and more overloaded and antsy. They were staring straight at him and couldn’t see it. To me out the corner of my eye his movements were more stiff and jerky.
I remember another time giving a talk to a group of parents. A boy was wandering in circles around the room. He soon walked straight up to me and stared straight at my communication device for the rest of the presentation. They said they’d never seen him do that to anyone before. He wasn’t super similar to me but he’d clearly seen a commonality between us.
I’ve seen classrooms full of autistic people with no ability to speak or type, who still clearly were interacting with each other all the time. Each of their files said that they never interacted with each other but only teachers. The teachers couldn’t see what we could see.
This is because the communication gap between autistic and nonautistic people is mutual. Yet the blame for that gap is placed entirely on the dysfunction of the autistic person in the interaction. The reality is it’s two people with different perceptual systems, different thinking systems, and different movement systems. The misunderstandings go both ways. When nonautistic children are taught to interact with autistic children, autistic children suddenly look more interactive. (This is an actual study.) It’s not because the autistic people suddenly learned social skills, it’s because the nonautistic people did.
What I describe above is how it is for someone like me. It’s different for every person. I wish I could tell you everything I know (I’m the only person I know who actively collects information on this) but it’s hard. And I’m tired and ill and my brain hurts. But I felt it was really important to tell you what I could because very few people out there are told about this. It isn’t an absolute but it’s extremely common.
Also — link — Alien Contact. An article by an autistic person about subtly communicating with an autistic woman he met in the supermarket while the woman’s mother was oblivious. Reminds me of a time I met someone who circled around my table once to indicate noticing me and my rocking pattern instinctively changed in response, which she correctly took as acknowledgement. (We talked later. At the time we were both far too overloaded for using words.) Jim’s whole website has a lot of good information about how autism is experienced (by people like Jim) as opposed to how most people assume it works.
And you’re right. The fact that this happens means a whole lot about autism. It changes everything. Most people aren’t paying attention but stories like this happen everywhere daily when two people just alike enough meet.
THIS
This so much.
I’ve seen this time and time again.
And as for appearances/functioning levels:
One of the people I can communicate almost-effortlessly with is my beloved. (Although not at the highest level of ease, but being very familiar with eachother helps) And he looks very different than me. (He’s very articulate for one thing :P)
And I’m sure others could give their own stories.
I agree with everything that others have said, though unfortunately, I know very few people IRL who are on the spectrum. In any case, I get along with people not based on some presumed functioning level, but the nuanced ways in which we communicate. I love communicating with people in general who aren’t very good with spoken language, because I’m not, either. Talking to people in a group is terrifying to me, but if I’m texting, sending emails, or having other communication that relies on typing for the most part, that’s perfect for me.
And whoever said this above — I do relate to some allistic people better than I relate to certain other autistic people. Perhaps it’s because my spouse is allistic. Perhaps it’s because the majority of people I have to interact with on a weekly basis are allistic, so I’ve been conditioned for the past 30 years to interact with all sorts of people. But finding people who are autistic who communicate on a similar level (and this isn’t about just verbal/nonverbal and body language; it’s something deeper) to me is like coming home. It’s like feeling comfortable in your own skin. That desire to belong and realizing that you do? That’s probably what is going on in the OP.
I don’t think I have anything to add that hasn’t already been said in OP and comments. So!