Astramentha

Hey you.

@ygpgsgl-public-records-only

You stalking piece of shit.

That thing you just posted?

That's pretty much direct libel.

Since you like screenshots and proof so much, here you go. A screenshot of the Merriam-Webster definition of libel!

And so you don't get away with erasing or editing this, I'm copy-pasting this here! Because this isn't block evasion, you slimy little bastard, this is self-defensive.

This IS an unjustly unfavorable impression. This is WRONG and HORRIBLE.

Newsflash, asshole.

The reason Bluesky banned you isn't because they don't care about victims, it's because they do -- They cared about Yomi, and all the shit you put her through. Your account was directly dedicated to talking shit about her and spreading lies. It was a prong of a direct harassment campaign.

Get off your high horse, you bastard.

You're a moral monster. You spew pseudo-philiosphical garbage while striking at a vulnerable person with a closed fist and blame her for everything that you do.

Get bent, you self-righteous little prick.

By the by, just so so all of you good people know, what's below the cut is a disgusting, abusive fake interview where this piece of shit puts words in a good woman's mouth and is an ableist piece of trash.

Freyja is for those who have been abused and long to reclaim their personal autonomy and power.

Freyja is for those who want to explore their sexuality in whatever way that means to them.

Freyja is for sex workers, and watches over them.

Freyja is for the sex-neutral, the sex-indifferent, and the sex-repulsed, because knowing your comfort and needs are important.

Freyja is for those who want romance, or don’t. Freyja is for those who want sex, or don’t. Freyja is for those who want one but not the other, and Freyja is for those who want neither.

Hell, you can be absolutely right, and in a year she’s gonna laugh and say ‘haha I thought I liked men, can you believe it?’ And you can still keep your damn mouth shut

Let every girl explore and discover her identity at her own pace in her own way.

Let every girl choose the labels that make her the happiest and most comfortable

I id'ed as pan ace for half a year before I started seeing myself as a lesbian. And honestly, had someone tried to chew me out for that or called it a phase I would’ve been crushed.

I can only imagine how much worse it feels for actual bi and pan girls

Let bi girls be bi girls and let girls-who-you’re-pretty-sure-are-not-actually-bi be bi girls because that’s their label to pick.

I would like to point out that this moment right here is so cleverly put and genuinely beautiful that it could work for everything people want and need to take from it.

I legitimately cried, because I didn’t only see how a healthy and respectful relationship should work, I also saw a beautiful and respectful way to legitimate and support asexuality, which is something I’ve never seen in a show, especially related to a same sex couple (a lesbian one nonetheless).

As an ace lesbian this means the world to me, because I always have to deal with over-sexualized characters and stories, and though I’m kinda used to it by now, it still bothers me, because I just wish people understood that not everything revolves around sex, and that you can be in a healthy and happy relationship regardless of it involving sex or not, as long as you really love each other.

I’ve been holding on to this for a while. In… September? I was having a Really Bad Time. So I ended up making this comic to sort of… sort through some stuff. It really helped.

I hope maybe it can resonate with other people, too.

Outpost

Question from an anonymous reader:

I regularly babysit a 3 (almost 4) year old who has Autism. He does not speak, and he doesn’t yet have a reliable alternative form of communication like signing or AAC, though he probably will soon.

 I have a lot of friends and two cousins who have Autism, but they all speak or sign. I find it difficult sometimes to understand what the kiddo in question is thinking, or wants, and I wondered if you or any of your followers have any first hand tips or advice on how I could better understand him? 

I know everyone is different, and I’m learning to read things like his body language, but I wondered if you/any of your followers who don’t speak or spoke later than most remember anything that helped them get across what they meant when they were younger, or things adults did that were especially helpful. He doesn’t have the coordination to sign or draw what he wants yet, being so little. I want to help him feel less frustrated and to be as good a babysitter as I can be.

Realsocialskills answered:

For the sake of readability, I’m going to call your cousin Anthony in this post. 

The first thing I’d say is: Listening to Anthony matters whether or not you succeed in understanding him. You may not be able to figure out what he is thinking, he may not yet be able to tell you — but you *can* treat him as a person who has thoughts and feelings worth listening to. That matters in and of itself, and it also makes successful communication much more likely.

Learning to communicate is really hard, even for typically developing kids. (Which is a reason why two year olds have so many tantrums, and why older kids usually grow out of that.) In early childhood education, a lot of what kids learn is that it’s possible to communicate in ways that others can understand — and that words are usually a better option than freaking out. One of the main ways early childhood educators teach kids these skills is by listening to them, and by supporting them in understanding the feelings they’re having. 

Kids with communication disabilities have more trouble learning to communicate in ways that others can understand — and they also often have more trouble learning that communication is even possible. Disabled kids need *more* exposure to adults who want to listen to them, and *more* support in understanding their feelings — but they often get less of both. Their feelings are often ignored, and their communication is often treated as nonexistent. 

All too often, kids with disabilities learn young that no one wants to listen to them. They often try their best to communicate, only to have their attempts interpreted as random meaningless noise or deviant misbehavior. When nobody listens, it becomes really hard to keep trying. One of the best things you can do for Anthony right now is help him not to give up.

It’s important to keep in mind that Anthony is a person with a perspective of his own. Our culture socializes us to see people with disabilities as having needs, but not thoughts or feelings. That implicit bias goes really deep for almost everyone, including AAC experts and long-time disability rights activists. Be careful to treat Anthony as a person with thoughts, feelings, and questions. This is a profoundly countercultural attitude. You can’t assume that it will happen by itself; you have to do it on purpose. (I did a presentation on this for medical providers a while ago which may be of interest.  )

Some specific things you can try:

Say explicitly that you’re trying to understand, eg:

“I don’t understand you yet, but I’m listening”.

“I’m not sure what you mean, but I do care”.

It doesn’t go without saying — and sometimes saying it makes a big difference!

Look for actions that might be intended as communication:

Does he point at things? Lead you to things? Flap differently under some circumstances?

Make a guess about what you think he might mean, and act on it.

It can be worth using words to describe what you’re doing, eg:

“I think you want the book because you’re looking at the book. I am getting the book”.

“I think the light is bothering you because you’re covering your eyes. I am turning off the light.”

He can’t read your mind, so it might not be obvious to him that you’re acting on what you think he’s doing — so tell him!

Name feelings you think he might be having, eg: 

“Susan took your truck. You are mad.”

“You like the marbles. You are happy.”

“Jumping is so fun!”

“You don’t like that texture.”

(Nb: Telling *adults* what they are feeling in these terms is usually *not* a good idea, but it’s a pretty common method used to help little kids learn about feelings — *if* you know with reasonable certainty what their feelings are.)

Ask questions, and offer choices, eg:

“Do you want the red shirt or the blue shirt?”

“Should we read the princess book or the truck book?”

“Should we go to the swings or the sandbox?”

Even if he can’t respond, being asked matters — it shows him that you care what he thinks, and that there’s a reason to try to communicate.

It can help to make the options more concrete, eg:

He might be more able to tell you which shirt he wants if you’re holding both of them. 

Or if you’re holding one in one hand and one in the other.

Or if you put them down in front of him.

If he responds to your question in a way that you think might be communication, respond to it as communication: 

Eg:  “You pointed to the dragon book, so we’ll read the dragon book”.

Or it may make more sense to just start reading it. Sometimes that works better than inserting too many words. 

Eg: “Ok, we’ll go to the park”.

You can also try yes-or-no questions:

“Do you want to go to the park? Yes or no?”

“Do you want to read the dragon book? Yes or no?”

“Is the dragon scary? Yes or no?”

“Is the king silly? Yes or no?”

Again, even if he can’t respond in a way you understand, trying matters.

You also might be able to teach him to point to things:

Pointing doesn’t require motor skills on the same level that writing and drawing do.

Again, in the two book example, you can ask him to point to the one he wants.

You can also show him pointing by doing it yourself, eg:

Take two books, and say “I choose the dragon book”, point to it, then read it.

Take two books and ask him “Which book do you choose?”

(Etc: It can take some time and trial and error to figure out how to teach this in a way that sticks, but it’s often worth trying.)

If he has a way to communicate “yes”, and “no” or choose between options, you can also check your guesses more directly:

“I think you said park. Am I right?”

“Did you say park, or something else?”

“Are you trying to tell me something, or are you playing?”

Remember that words can be communication even when they’re unusual: A lot of autistic people use idiosyncratic language to refer to things, or repeat phrases they heard somewhere else – in a way that they may or may not mean literally. Here’s a method for noticing when repetition is communication , and some thoughts on listening to folks whose speech is unusual.

Give him time to process and respond:

The standard teaching advice is: When you ask a question, wait at least seven seconds before you say anything else.

This feels a little unnatural — it can feel like a *very* awkward pause, and it can be tempting to jump in and say more stuff to clarify.

But if you say more stuff to someone who is thinking and formulating their answer, it tends to just give them *more* stuff to process. 

So give him time to respond — and be aware that autistic people often need longer to process and respond.

If you have an iPad you’re willing to let him play with, iPad use can really help some kids with motor skills and learning communicative cause-and-effect.

Most kids learn pretty quickly how to scroll through select the app they want, and that skill often transfers.

Most kids that age like Endless ABC, a really fun pre-literacy words-and-spelling app. https://www.originatorkids.com/?p=564

(That app also builds an association between interacting with a touch screen and making meaningful sounds)

You can also try the Toca Boca apps — a lot of kids like those, and some, like Toca Hair Salon, don’t require particularly strong motor skills.

Often, the best way is to play with the app together — eg, you show them how to drag the letters around, then offer them a turn.

Or help them out when they get stuck, without taking over.

Or say things like “which color should we pick? How about purple?” and see how they react.

Don’t expect AAC to fix everything:

Everything in this post still applies once he gets a device or a system.

An AAC device is just a tool. It’s one mode of communication, which might be useful for him under some circumstances.

Having an AAC device will not make him instantaneously able to communicate using words in the way that typically-developing kids his age do.

While some people learn to use an AAC device fluently very quickly, that is rare. 

Most people who use AAC because of a childhood speech delay take a long time to learn it.

And in any case, giving someone a tool doesn’t cure their disability. 

An AAC user with a communication disability still has a communication disability, and disabilities that interfere with speech sometimes also interfere with language. 

Even people *without* language disabilities tend to take a while to learn, for all the same reasons that typically-developing kids take a while to learn how to use words to express themselves. Communication takes practice.

(And also, all existing AAC technology has significant limitations and difficulties. It’s easier for typically developing kids to learn to speak than it would be to learn to use AAC, and having a speech disability doesn’t magically make AAC use easy.)

AAC implementations can also end up treating AAC use as an end in itself and forget that the point is to support communication. 

For most AAC users, AAC is one communication mode among many they use, and it’s not always the best one in every situation — eg: pointing to a banana can be a *much* more efficient way to communicate than scrolling through a device and finding the “I” “want” and “banana” buttons.

If Anthony gets an AAC system, he will still need you to put effort into listening to him, and he will still need you to take all of his communication seriously.

Remember that disability isn’t bad behavior, and don’t be mean:

Don’t ignore his communication in order to force him to talk or use a system.

The best way to encourage communication is to listen!

He’s not struggling to communicate because he’s lazy; he’s struggling to communicate because he has a disability.

He’s doing something really hard, and he’s in a hard situation, and that needs to be respected and supported.

You don’t need to introduce artificial difficulty; he is already experiencing more than his share of the real kind.

Anyone else want to weigh in? What is helpful for effective communication with a nonspeaking four year old?

“My name is Robert Lee IV; I am a descendant of Robert E. Lee, the Civil War general whose statue was at the center of violence in Charlottesville. We have made my ancestor an idol of white supremacy, racism and hate. As a pastor it is my moral duty to speak out against racism, America’s original sin. Today, I call on all of us with privilege and power to answer God’s call to confront racism and white supremacy head-on. We can find inspiration in the Black Lives Matter movement, the women who marched in the Women’s March in January and especially Heather Heyer who died fighting for her beliefs in Charlottesville.”

some ableist fool who knows naught of magic: if you’re so tired, how come you can [stim/talk about special interest/scroll through tumblr]– you must be faking! you just don’t want to do it