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Friendly Neighborhood Autistic

@autist-tips

All are welcome!
early 20s, aro ace, female
Interests: MHA, Genshin, BTD(B), SU
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The Autism Acceptance Month Week-long Celebration starts tomorrow!

April 24th through April 30th I will be posting daily autism-related content! While I will not be posting additional requested content during this week, feel free to send in asks and requests! I’ll be responding like usual, and I will start filling requests I receive after the celebration ends. 

This is your reminder to turn off notifications or block the celebration tag if you are not interested or do not want to be spammed! All content posted during this week will be tagged with #autism acceptance month

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autist-tips

So I have a question for you or your followers.

I'm autistic and I'm working on becoming a teacher over the next few years. Thing is, I haven't found many resources for autistic teachers. I'm having difficulty coming up with lesson plans and getting my point across. Anxiety is also making me shut down a little bit.

If anyone has any tips or resources, that'd be much appreciated.

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If anyone has a response for @lollipopdollie and wants to send an anon ask, I'll be watching my inbox for responses.

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Advice originally about something else: it's always easier the second time around. When tutoring, I found it true that I would get more comfortable teaching a topic as more students asked me about it. (I tutored math for two quarters in college, but am not a teacher.)

Eureka Math has (almost) minute-by-minute scripts of their lessons, for free. It seems a lot of neurotypical teachers hate how inflexible the scripts are. It sounds like lesson scripts are just what you need. I don't know if they have scripts for their other textbooks, though.

Anyway, you don't have to be good. Just good enough. They were in their school's general college preparatory program. As a tutor, I just had to be better than the student's professor. Not even better at the subject matter. Just better at listening to their questions and understanding where their confusions are. Teaching strategies that include frequent quizzing/testing are meant to help with this.

Also, a quick little tip: if a student asks a question and doesn't seem helped with your answer, ask the class to answer the question. Usually another student had the same question/thought process already and can explain clearly. If not the answer, at least they can try to rephrase the question for you since, again, there's probably other students with the same question. This will help you keep the class moving instead of getting stuck on a question.

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amaraqwolf

Are you trapped on tumblr right now?

Is there something you planned to do before you got trapped in the endless tumblr scroll?

Are you yelling at yourself to get up and do the thing, but you can’t, because you’re trapped in the endless tumblr scroll?

Consider this your save point.

Put tumblr down, stand up, stretch, and go do the thing you planned to do. Future you will be incredibly grateful.

Things people in the notes have been able to do thanks to this post:

  • eat breakfast
  • go to bed
  • get out of bed
  • take a shower
  • write
  • practice
  • watch Superman Returns and write a paper on it
  • retain shreds of sanity

I need y’all to know that you’re doing amazing, and I’m so glad that I was able to help you break out of a procrastination loop you did not want to be stuck in.

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Hello! I have ADHD/Autism and I just realized this coping mechanism I accidentally developed. Thought I'd share in case someone finds it useful. When my symptoms are acting up and I need to ask someone to do something because of it, I've found it easier if I state the symptom rather that the condition.

For example, I work in customer service. When I don't quite catch what someone says and need them to repeat it, I tell them I have an "auditory processing disorder" as opposed to saying ADHD or Autism. People often don't know enough about either condition to understand all the symptoms, but stating the symptoms themselves makes it more clear. It also helps avoid any prejudice or stigma I might get from these random people if I say I'm ADHD or Autistic.

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Yes, this is good advice!

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Please forgive me if you've answered this before, but as a fellow aro/ace autistic person, have you ever felt like the people who accept you as being aro/ace do so specifically because you're autistic? As in, they think that's understandable because autistic people are often seen as being incapable of romantic or sexual love or feelings? I've experienced that with some family members, so I wondered if that's an experience you may have had too

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I don’t believe I’ve answered this before! Personally, I’ve never had this happen to me. The only people that know I’m autistic+aroace are people that are neurodivergent and are respectful of the aro/ace communities. Other than that I don’t really tell people.

When it comes to family members, they just know I don’t want to date anyone and are fine with it. So this isn’t something I’ve experienced, but I’d imagine I’m in a minority in this situation.

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PSA to neurotypicals:

For the love of god stop playing the pronoun game.

It is infuriating to try to follow in a conversation where you refer to people you haven’t mentioned we’re talking about by pronouns, then get mad at me when I don’t understand.

I just had a conversation with my sister like this. Here’s how it went.

Me: Who was at the door?

Her: It was [mom’s ex].

Me: What did he want?

Her: I dunno, but since Mom’s not home (something happened at her work) he’s coming back later.

Me: Okay. When she gets home I need to go to [place.]

Her: Okay. They’re going to the mall.

Me: But I just texted mom that i need to go to [place.] Why are they going to the malll?

Her: No, they’re going to the mall now.

Me: What??

She meant that my mom’s ex and his two son’s were going to the mall. How was I supposed to know that ‘they’ referred to two people that I hadn’t been told were there? I assumed ‘they’ referred to, you know, the two people already mentioned?? (My Mom and her ex.)

This is how all you neurotypicals sound when you talk. Mention people by name, stop using pronouns like ‘they’ unless you’ve already established who ‘they’ are.

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Hey, quick tip for messaging your neurodivergent and/or chronically ill pals:

If they do not respond to you right away or in a little while, please do not keep spamming them with messages until they respond. They could be dealing with a flare up or might be focused on something else atm. Texting and messaging people can also take a lot of energy, especially when we’re in pain, and if you keep adding message after message you’re making it more difficult for us to actually get back to you because you keep giving us more that we have to respond to.

I know it can feel this way, but when we temporarily “ignore” you (and I use that word very loosely) this does not mean we suddenly don’t love or care about you. We’re just fatigued, in pain, experiencing a mental block, etc. and we need extra time. Just give us a little breathing room, we’re already suffocating.

Neurotypical and able-bodied people are highly encouraged to reblog this, just don’t clown.

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This happened two times today so I'm just gonna say it.

Person A: "take those boxes downstairs"
Me: "ok, do you want me to put them in recycling?"
Person A: "Break down the big box and put it in recycling."
Me: (breaks down big box, puts it in recycling, puts other boxes down stairs"
Person A: "why did you leave those boxes downstairs? Didn't I just tell you to put them in recycling??"

The other example that happened moments after:

Person B: "put a cup of rice and two cups of water in the pot"
Me: (puts a cup of rice and two cups of water in the pot)
Person B: "Did you turn the burner on so the rice can cook?"
Me: "No, you never told me to do that so how was I to know?"
Person B: "use your brain"

If you don't tell me what to do or how to do it I'm not going to know or understand what you mean or what you want me to do. I really don't see how neurotypicals even do this because it makes no sense to me. Like if someone said "brush your hair" I'm not going to assume they meant "brush your hair, straighten it, then put it in a ponytail" now am I?

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An autistic friend of mine just said this to me “The harder I work at communication the more people expect from me and the less they are willing to compromise.” and it is the most fucking heartbreaking thing I’ve heard.

This is very much a thing, though - and I’m sure people across the board with other disabilities can verify that it happens to them, too. People will turn any progress you make toward being “normal” - no matter how straining or difficult it is for you, no matter how little it actually helps you - as either inspiration porn, or proof that you don’t really need accommodations, you just need to “apply yourself! :)))))”

YUP

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kipplekipple

And they do NOT get that just because I can do something one day, doesn’t mean I can do it every day

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Autistics tip #6

A checklist of some common things that could be causing that ‘something is wrong’ feeling you sometimes have but don’t know why.

1) Are you hungry?

2) Are you thirsty?

3) Do you need to use the bathroom?

4) Are you physically tired? Do you need to lay down?

5) Are you sleepy? Do you need to take a nap/ go to bed?

6) Do you feel sick? Maybe your stomach? A stuffy nose?

7) Are you in pain? Does your head hurt? Does a muscle or joint hurt?

8) Are you stressed or overwhelmed?

9) Are you understimulated?

10) Are you anxious or upset?

11) Are you too hot? Too cold?

12) Do you feel icky and want to get cleaned up?

13) Are you socially exhausted while you’re in a social situation?

14) Do you need to stand up and stretch/walk around?

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idk who else to ask tbh so i’ll ask you. is wanting to memorise things an autistic thing? like i know a bunch of facts i’ll never need to know and i know the first 50 digits of pi by heart

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Yes, this can also be an autistic thing! Autistics generally love to learn new information because it helps us feel more grounded in our environment. We like to understand things, even if the stuff we learn is kinda random.

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Idk if I'm allowed to ask this here but is not being able to tell the difference between being hungry, full, thirsty and nauseous an autistic Thing? because I've always kinda had this problem, I eat based on what time it is not whether I feel hungry, and sometimes I think I'm hungry but actually I just need water (I end up skipping meals on accident a lot too whoops)

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This can absolutely be an autistic thing! When I was younger I struggled to tell the difference between thirst, hunger, and sickness too. I still do today, I’m just getting better at using deduction to guess what I’m feeling.

I eat on a schedule because I sometimes don’t feel hunger until my blood sugar starts dropping, so you’re not alone with that.

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hey I'm trying to spread awareness for a film that's struggling to meet its goal and its about to run outta time to fundraise. its about dating on the autism spectrum and its written directed and performed by an autistic woman who's planning to release it for free on youtube if you could share about this it would mean the world to us its on Indie Go Go under A Simple Date (with dots after A S D)

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From the time I’m posting this, there’s only ten (10) days left for fundraising and they’re only at fourteen percent (14%) of their goal!! If you guys can, please go donate and help out the cause!

Here’s the link to the indiegogo page:

Please reblog and spread the word!

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This is painfully accurate

Look into them more. The stuff they have advocated for is straight evil. Suggestions genocide, claiming autism is both infections and a terminal illness. Plus more. They are like the Peta of people.

Saw someone with an “Autism Speaks” Shirt in my school…..in my school of all places, a FUCKING SCHOOL FOR THE DEVELOPMENTALLY DISABLED AND PHYSICALLY DISABLED 

All they do is silence us while claiming to speak for us. 

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Does anyone else with auditory processing disorder find it easier/harder to process different languages?

I speak English and Spanish, but unless I’m focusing and lip reading, I can’t understand what people are saying. BUT I’m also learning Japanese (because I can 😝) and it is 1000x easier to process than the two other languages I have more experience with. I don’t know what the words mean yet, but I can actually hear them instead of doing the guessing game I usually do.

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idk if you take these sorts of questions but i need some advice?? im supposed to be starting 'work' (my mum is just making me work round the house and paying me. normal work hours) on monday and im really just. too disabled to be doing this. ive had meltdowns everyday since finding out and i haven't even started yet?? i know i won't be able to do 8 hours since i couldn't even do 6 when at school/college. do you have any advice on how to bring up my concerns about this to my mum cus i got no idea

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I don’t have much advice for this. I would say that you should tell your mom about the meltdowns and your concern about the hours and see what she says.

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gayboybeetle

hey would anybody with autism (and who is touch hypersensitive) mind telling me how being touched affects your daily life? like... how does it feel when people touch you (maybe hugs or shoulder pats)?

im curious bc 1) I might have autism??? (still trying to figure that out) so I'd be interested in seeing if i relate and 2) I'm writing a character with autism who is touch sensitive so i wanna be accurate :)

Ok so, to me, being touched makes me feel very bad, a chill goes over my body and it's very uncomfortable, specially with light touch

Depending on how/by who/where I'm touched, I feel like I'm being violated and immediately start crying and shaking (maybe I have meltdowns? I'm still not good at defining it)

I'm very ticklish, idk if it had anything to do with it

Not all touch is bad, it really depends. For example, I like being hugged by people I trust. I like the pressure of a tight hug.

It quite affects my daily life as it's common for people to touch each other friendly in Brazil. People, specially adults, will hug me, touch my hair, tickle me etc. And because it's so common, people don't understand when I tell I don't want to be touched, and will think I'm just being rude. So most of the time I just have to endure the touch because I have no choice.

Going to the doctor is specially terrible, as doctors will have to touch you to see if you're okay.

I hope I haven't rambled too much! These are just my experiences as an autistic person

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autist-tips

I can only handle being touched by people that I trust, but it has to be like, an actual touch. Like there needs to be pressure. When people just barely touch me or brush up against me it’s the worst feeling ever. Bad touches cause me to feel overwhelmed almost instantly and they start meltdowns pretty fast too.

Doctors don’t bother me all that much. I don’t like it when they touch me, but they do it ‘right’ so it’s not sensory hell.

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