#aba cw

[tabby-shieldmaiden]

Watching a bunch of Patricia Taxxon videos all at once does something to your brain.

[materialistvampire]

Not to be controversial, but sometimes I get irritated by the way that online discussions about autism are mostly dominated by people diagnosed in their late teens/20s/later in life, or people who are self-diagnosed. Not because I don’t think there isn’t any value in discussing that experience, but I feel like it leads to a sort of... fantasy about what early diagnosis looks like that is often wholly disconnected from what the reality is.

Like there seems to be a pervasive idea that “if only I’d been diagnosed early, I would’ve been able to get proper accommodations as a kid/known what was up with me”, and like, as someone who did get diagnosed young (as an AFAB person, I will add, because I see this more among AFAB people, who yes do have a serious issue with being overlooked for diagnosis) this just does not check out with my experience and that of people who were diagnosed at young ages at all?

Like it’s well known that neurotypical people just generally do not know much about autistic people. If you’re diagnosed young, that does not mean actually getting accurate and detailed information about what that means. Even assuming you have fairly well meaning parents who are willing to share with you information about your diagnosis (and not, say, use it as a pejorative against their kid//try and cure their kid’s autism), they themselves might not actually have that much information to share beyond whatever their doctor told them, and it is well known that the average pediatrician doesn’t really know a lot about autism. Even if they actively go out and research for themselves, it’s very likely they stumble upon things like say, the Autism Speaks website, or other resources aimed at parents in their situation, which are most likely going to be about as helpful as that implies (read: not very).

And when it comes to the matter of accommodations, the fact remains that oftentimes kids don’t actually have a say over what accommodations they get, and more importantly, the parents who do have a say very frequently do not know what their actual rights are.

For instance, let’s say your kid has an IEP. A parent may not be told that they have a right to schedule an IEP meeting at any time, that they can request any sort of amendments or accommodations to be put on them, and that school officials have to comply.

Did you know IEPs often have goals attached to them? Very often the answer is no, but let me tell you, from what I remember of the IEP meetings I did sit in on (which I was only able to do starting in middle school), the “goals” aspect was much more emphasized than the idea of accommodations ever was. And generally those goals are things such as “turn in X% of assignments on time”, or “make eye contact X% of the time”, or other things along those lines. Essentially trying to pressure kids into meeting a certain threshold of neurotypical behavior. These goals basically almost always are recommended by special ed officials at the school.

It was never told to me that I had an ability to get rid of those goals in any way other than by meeting them, and my parents didn’t seem to realize they could either. Even when someone else outright told me those things were, in fact, amendable, I didn’t believe them because no one ever indicated that was possible.

The system doesn’t work by handing a kid a menu of potential accommodations and letting them pick which ones they think would be helpful. Accommodations are often picked out by schools (with some input from parents, but unless a parent has specifically researched accommodations, they’re probably just gonna go with whatever is on the list). And beyond the fact that kids aren’t always even told what is on that list, it can also include things like “social skills therapy” that is basically ABA-lite (which yes, speaking autistic kids can get put into, it isn’t only nonspeaking kids who end up in that sort of thing) or kids getting assigned paraprofessionals whose whole job is to stalk them and report on their behavior, or in some cases, attempt to “correct” it, something which actively leads to greater social isolation for said kid.

To speak for myself personally, I was told that I suffered from executive dysfunction (which let me tell you, not even every autistic kid gets told that), but that it was very much a personal failing that could be solved by “being more organized”/”trying harder”. There was never any mentions of the idea of ableism - if I was being socially ostracized, it was my fault for having poor social skills and I needed to learn better ones in order to fit in better, which on some level can be helpful for kids, but when that includes things like “making forced eye contact” and “being less oppositional” then that takes on a decidedly different angle than just helping a kid with social skills. A lot of the information I know about autism now doesn’t come from anything I got told due to my diagnosis, but my own research on my condition that I undertook much later in life.

So it is immensely frustrating to me to see people talk about early diagnosis as if it would have somehow led to them being more supported and more understanding of their experiences, and that’s just really not true for the vast majority of people. Unless you had a parent who was willing to do the research and listen directly to you over any of the so-called “experts”, or a special ed person/team that knew a lot about autism and how to properly interact with and help autistic kids, you probably were going to end up in a situation that varied from not much different from being undiagnosed/actively traumatizing in entirely different ways than being undiagnosed is.

I understand the idea of being able to go back and properly support your younger self, especially in terms of healing, but I think it’s also important for people to understand that the experience for actual autistic kids who get diagnosed young is not how diagnosed-as-adults people typically imagine it as being, and I really wish that there was some sort of wider acknowledgment of that.

[tw-slugass]

mmmm yummy aba abuse propaganda sites talking about autistic people like they don’t exist past the age of like 12 when i’m just trying to fucking google features of autism yummy yummy in my tummy!!

[system-of-a-feather]

Maybe when I get my PhD Ill research long term effects of "good and modern ABA" and burn it to the ground Round 2 Electric Boogaloo /hj

[asdcats]

Not often I find an essay/analysis of my spin from an autistic perspective and this ones really good. Hope she does one for the tv show as well.

[birdofmay]

I am autistic but have severe trauma due to masking (I’m an ABA victim) and so unmasking has been difficult. Lately I’ve been more open and learning that I don’t need to respond to something if I don’t know how to respond to it. A lot of times it’s “I apologize your words affect me deeply I just don’t know how to respond to that :(“ and I genuinely feel terrible that I can’t find my words or find the way to appropriately connect my feelings to a response. Before this I used to be like “I’m appreciative of that, thanks.” Or “I don’t really like that…” but things have become more complicated and now I don’t want to use the default template response because it doesn’t actually connect to how I really feel. Is there some term for this? What is it? I don’t think it’s nonverbal or nonspeaking I mean I can talk and such, I just don’t know what to completely say to people or what genuinely feels ok to say that is satisfying to how I feel internally. A piece of me feels a little restricted with only learning one language (english) and I feel that other languages out there have better ways to articulate and connect how one internally feels.

I tried to reword your ask and if I understand you correctly, what you're basically saying is

"I used scripts all the time, and now that I'm not scripting anymore I realised that I don't know how to express myself and my feelings"

did I get that right?

If so, I think it's very common to struggle with that in the process of unmasking. Once the reliable scripts are gone, you have to figure everything out yourself, and of course that's confusing and frustrating. But I don't think there's a special term for that.

I'd like to hand this ask over to autistics with similar experiences, no matter if you're a follower or not, feel free to comment whatever comes to mind! ☝🏼

[smiff-spike]

sally anne is no friend of mine

there’s a table and a woman and a box and a ball and she’s asking you where the ball is, where someone else would say the ball is, where the ball should be, if x is box minus ball over perception times entitlement to absolute truth solve for number of things confiscated when the answer given is not what she wants to hear

define truth as (noun) whatever the authority figures say, define authority figures as (adjective) having the power to confiscate belongings, bind hands to chairs, cast verdict on who is correct, who is deserving, who is a person, define person as (noun) a locked door, an open field seen only through a window, an unattainable freedom

define things as (adjective) to have agency, to be believed, to have autonomy, to be listened to, to be respected, to spend time with favourites with no strings attached, to have an unlimited choice of hand movements, to be comforted when upset, to not be upset on purpose, example sentence: these things will be confiscated if it cannot be demonstrated they are deserved

if school is minefield plus blindfold over open bracket effort divided by recognition close bracket minus expectation of failure solve for maximum length of time until total burnout

if child is set up for failure, when they don’t succeed is that a. the child’s fault b. the child’s fault c. the parent and the child’s fault d. the child’s fault?

if the ball is taken out the box unseen, and no one mentions it happening, then a. this is a trick question b. this is a trick c. there is no right answer d. everyone knows where the ball is e. outside everyone else is laughing,     the sun shining, where is the ball?

[autisticadvocacy]

Invisible Abuse: ABA and the things only autistic people can see

One of the most hotly-contended points of division between the adult autistic community and the neurotypical parents of autistic children: explained.

Content warning: Videos of ABA

“No electric shocks, no aversive, nothing to make the experience traumatic, right? Wrong. Allistic people can’t see it, because they don’t understand how it feels to be autistic.”