Connie had bought into the toxic and ableist narrative of scarcity mindset. It is based on the narrow view of disability that means people are disabled based on how easy disability is to see from the outside.
Connie believes there is a very narrow way to be disabled, and when someone isn’t disabled the way that her child is, then they are a threat to the scarce resources her child may have access to. This is partially true. Resources are hard to obtain if you don’t seem obvious enough
If you have basic motor control, can speak fluently, can read, and you can answer basic questions about yourself, then you can work in the eyes of the state. This isn’t what prevents most autistic people from being able to maintain a job, though, or from being self reliant.
Do they have the auditory processing speed to keep up with spoken words? If not, then that rules out most low paying jobs.
Do they have the vestibular stability to bend over and stand up over and over? If not, that rules out tons of jobs.
Do they have the executive functioning and working memory to be able to do novel tasks that require multiple steps? If not, that rules out most jobs?
Can they function with the noise level of most jobs? Are there social dynamics at play?
Is there a lot of task switching? Do they have the executive functioning to adapt quickly enough for new tasks all the time?
Do they have co-occurring conditions like epilepsy, IBS, Ehlers Danlos, lupus, mast cell activation syndrome, etc.? Are they able to work some days? Are those days predictable by any metric?
Have they already tried to work without accommodations for so long that their brain and body have such severe trauma that walking into a workplace would be harder than walking into a burning building? <<Because that’s where so many autistic people are.
Someone isn’t a fake autistic or non-disabled because they can type words. People like me can really only type words (but not even consistently) or read words, so we develop that skill out until we are pretty good at it. But abled empathy fails us.
Most non-autistic people have a very flat ability profile. They are about equally as good at one thing as they are at other things. If they can not button their shirts or make a sandwich, they also can’t do complex math or compose orchestral scores. (An example of extremes).
Their brains have relatively evenly distributed resources. They think that all brains have relatively evenly distributed resources. IQ tests are garbage, but they do measure something (just not fairly). On an IQ, there’s more than 100 points difference in my subscales.
My visual spatial intelligence is in the intellectually disabled range. Verbal and memory were very high. I recently was determined to have auditory processing in the .1 percentile. My vestibular system is so hyporesponsive that it’s the equivalent of deaf or blind.
I can’t task switch. My executive functioning is abysmal. It’s not a moral failure or laziness. I could do one thing for days without a break— unless other people are involved. But I can’t just do something else.
I have speech disorders that are more apparent when I’m overwhelmed. They make me seem pedantic or robotic because I don’t pull language from the same place in my brain as most people. I can often ONLY retrieve academic/procedural jargon, which reads as cold in social settings.
But the result is that people like Connie, who think if someone like me “sounds smart,” then we are like neurotypicals and are good at most things. Sadly, they tend to think that people without verbal speech are bad at most things.
And when people see neurodevelopmental differences through a neurotypical lens, they think we are either really good at and capable of most things and are just quirky or we’re really bad at most things and are just in need of charity.
Disability accommodation and inclusion is not supposed to be about charity and handouts. It’s about accommodating people so that they are able to participate and contribute meaningfully in society and the world around them.

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More from @NeuroClastic

24 May
How do you feel about being tagged in a comment thread on twitter to have someone say something along the lines of “This person you follow is a problem and I hope you’ll do the right thing,” meaning to unfollow. Is it coercive or helpful?
Frankly, I hate it. I am not following a few thousand of my closest friends. I follow people because they said an interesting thing one time and maybe it’ll happen again, or I liked their profile picture, or I just hit “follow back” because I do that. I mainly follow autistic ppl
But mostly, Twitter puts the same few people in my feed over and over, and it’s not even always people I follow. What’s even the point of followers?
Read 4 tweets
30 Mar
Let's look at the harm of not listening to activists. From this platform, we have been talking about the injustices in Virginia Beach against neurodivergent and Black residents. We have dedicated a large amount of our resources and time to focusing on Virginia Beach.
On neuroclastic.com/freematthewrus…, we have highlighted-- solely using evidence from the prosecutor's office and @VBPD, the glaring human rights violations and mismanagement of handling Matthew Rushin's case.
We highlighted the injustices that happened to Champ Turner, a Black, undiagnosed Autistic father who was attacked by a 400 white man, got away, called 911, and was charged with and convicted of the same crime as Matthew Rushin neuroclastic.com/freechampturne…
Read 15 tweets
2 Dec 20
I was so bummed by #SocialStories that gaslight #ActuallyAutistic kids that I made one that is not traumatic. It’s for ALL kids because it’s not necessary or healthy for minority groups to assimilate against their wishes and neurology. Alt text added to each image. 10 slides Image Description 1: A group of 5 kids below which text read
Read 10 tweets
21 Nov 20
I want to apologize for my responses to the Sia movie. Nonspeakers had replied, but I didn't see it. It was erasing their input by asking people to listen to them. I also should have used my personal account and not the publication account. (cont)
My personal perspectives are very affected by my experiences & are not universal among our contributors. I am really sad for all the constant pain & erasure & misrepresentation autistic people experience. I definitely don't ever want to invalidate any of that. We deserve better.
I (Terra Vance) will do better to use my personal account to respond to things that are not an issue that is pretty universal among our contributors and apologize for not doing that. I made mistakes and missed things that were relevant to inform a full and fair reaction.
Read 4 tweets
21 Nov 20
I want to clarify a few points about my thread about the Sia movie because I think in my long thread, I still wasn't clear enough on a few points. I'll try to condense them to one thread at a time.
1. I wanted the point of the thread to be about how we as a community were addressing the issue was often using talking points and language that doesn't reflect the best language for nonspeaker rights.
2. Many of the things said about Sia were things that are tacitly ableist and can cause harm.
Read 17 tweets
21 Nov 20
I’m having a hard time with the discussion about the movie, Music, written and directed by @Sia. First, everyone is referencing NonSpeakers as “non-verbal.” NonSpeakers are nonspeaking because they are apraxic, and that means they can’t coordinate their movements to speak.
They often also can’t coordinate their bodies. They do things without being able to control themselves. Asking them to act in a movie where they have to do very complex ordered tasks would be overwhelming.
It can take a NonSpeaker a week to write an article because of the difficulty of spelling to communicate. But when we publish articles by nonspeakers, nobody reads or shares them. They are our lowest traffic demographic despite that I put 10x more effort in promoting them.
Read 32 tweets

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