#Aac user

[neon-emojiz]

Me with my machine in public to make you less scared of using yours!!

— At the mall

— Still at the mall, got food!

Image descriptions in alt text!

I didn't take a lot of photos, but I also used it in build-a-bear!! The staff were incredibly nice and treated me as if I was mouthspeaking!

I definitely recommend going to build-a-bear to practice with AAC

inspiration from @tontoemojis !!

[thecouncil-aac]

Be the change you wanna see in the world /ref

Lowkey, we want to add some Khmer to our board, but don't know how Coughdrop is going to handle that

Especially considering we can speak it, but can't spell for shit

-Nyomi

i !!!! want !!!!!! bilingual!!! aac!!! ich will mit meine schwester sprechen !!! auf deutsch!!!!

[stories-by-starlight]

Shout-out this stranger met for while recent, who saw we were AAC user and for whole time:

• made sure we not talked over in conversation

• stopped others from skip over us, and didn’t let them rush us either

• said any words AAC was say wrong verbally for us after we express frustration with that

• didn’t touch our device once or look at screen while using AAC (they were only person who didn’t)

• made sure we comfortable and accommodated whole time was with them

And don’t think any this was even big deal to them. This was first time they even saw AAC, but they still made sure were accommodated for it. Don’t think they realize how much meant to us, and it meant everything to us. To be include and supported so much by total stranger who we would never see again.

Gave us lot hope. Fact that there people like that out there. And wanted put all thoughts that couldn’t put into words when with person here.

Want other AAC users know that there people like that out there, and that there hope.

Edit: Notice this post a lot of people’s first time hear about AAC, want be clear that this person only start say words out loud for us after we made clear that that was something we okay with. Please don’t assume other AAC users want others correct words AAC pronounce different, because many don’t. Every AAC user different person with different preference, please don’t take ours as universal rule.

[alex2xander]

Be nice and don't mock tumblr users that communicate differently.

Examples:

1.) Typing quirks

2.) No punctuation

3.) Random Capitalisation

4.) Long run on sentences

5.) Frequently misspelled words

6.) Missing spaces between words

7.) Repeating words and sentences

8.) Posts audios and videos instead of typing

9.) Express themselves through custom emojis

10.) Use an AAC (Augmentative and alternative communication) device

Some users have intellectual disabilities, use speech to text, struggle with grammar, have hand tremmers, have high support needs, etc.

Regardless of how they communicate and their reason why, they still deserve respect. They are trying their best.

[five-thousand-loaves-of-bread]

autistic people dominate AAC conversation on tumblr so for this AAC awareness month (October), let us also remember all non-autistic AAC users & autistic AAC users who not use AAC because or solely because autism.

people use AAC for from intellectual & developmental disorders to neurocognitive disorders to neurological to physical disorders. people use AAC for disorders from birth & acquired disorders. progressive & non progressive disorders.

some AAC users have mouth speech, motor, and/or sound clarity related difficulties, others use for language and/or cogntive difficulties, some for combo of reasons.

those with…

intellectual disability

genetic & chromosomal disorders like down syndrome, rett syndrome, angelman syndrome, williams syndrome, etc.

cerebral palsy

speech language disorders like aphasia & dysarthria

schizophrenia & schizoaffective & schizo-spec

brain injury

dementia

amyotrophic lateral sclerosis (ALS), multiple sclerosis (MS), huntington’s, frederick’s ataxia, etc.

tracheotomy

locked in syndrome

n so much more not listed here

[clownrecess]

Happy disabled pride month to disabled people with undiagnosed physical disabilities

Happy disabled pride month to disabled people with undiagnosed mental disabilities

Happy disabled pride month to mobility aid users

Happy disabled pride month to disabled people who are in constant pain

Happy disabled pride month to AAC users

Happy disabled pride month to disabled people with ableist family

Happy disabled pride month to fat disabled people

Happy disabled pride month to disabled people with scars

Happy disabled pride month to disabled addicts

Happy disabled pride month to disabled people who's disability is progressing

Happy disabled pride month to disabled people who love their disability

Happy disabled pride month to disabled people who hate their disability

Happy disabled pride month to disabled people with underrepresented and/or uncommonly known disabilities

Happy disabled pride month to all disabled people. I love you. /p

[zebulontheplanet]

I get confused a lot. I think other people get confused too.

Talk about visible autism sometimes, talk about being visibly disabled. But when talk about it, always get low support needs people saying “yeah, I stim and people notice and stare at me. I’m visibly autistic sometimes”

And don’t think they understand when I say visibly autistic or developmentally disabled. Yes, know that sometimes “visibly autistic” isn’t black and white. Some people do get marked as visibly autistic just for stimming a bit.

But when I talk about visible autism, don’t talk about that. And it can be frustrating. Feels like people talking over me. Just want to scream “you don’t get it”.

Example: was in library yesterday. State Caregivers came with their clients, they sit in library, walk around, watch movies, look at books, eat lunch. They’re required to take their clients out into the community for a certain amount of hours a week, so why not the library? I was there. Was there with my caregiver. Looked over, saw the clients, and saw the caregivers looking at my caregiver with a knowing look. They knew. I knew. Their clients knew. I was like them, and they were like me. Just people sitting in the library who are disabled and require caregivers.

That’s what I’m talking about. That knowing look. That look of pity. That look to my caregiver that says it all. The looks of pity from the librarian. From everyone.

Visible autism for higher support needs autistic people, so much more different than visible autism for low support needs people. And that needs to be realized. Strangers know. And sometimes they don’t know what’s going on, but they all went to school probably, right? They know the special education kids. The “special” kids. Yeah. That’s us. That’s me. They know. I’m tired of people not understanding.

Yes, community. Find middle ground. You’re like me, I’m like you. We are all autistic (those who are autistic), but that doesn’t mean all experiences the same. That doesn’t mean we think, act, eat, sleep, the same. You’re different, and that’s ok.

[spooksforsammy]

Geniuenly like. So many people claim support disability. But then say something completely untrue

Y’all support autism? So what about when the person has intellectual disability or need help walk talk eat bath use bathroom? Does your support end when you see someone with higher needs?? Someone who actually genuinely won’t survive without support from others n that support is sometimes having other people do everything for them.

Y’all support depression? What about when the person can’t bring themself to get out of bed for days on end? What about when that person goes days weeks months without cleaning self because can’t get up even though need to?

Yall support schizo-spec disorders & psychosis? What about what the person get violent because of their delusions n hallucinations? The ones know are fake but still can’t help but believe in? The ones genuinely believe in their delusions/ hallucinations? What about the ones don’t don’t get violent to self n other because of the disorder? Those that just sit scared about the hallucinations n delusions. The ones that won’t leave their room/ house out of fear of their delusions/ hallucinations?

Y’all support those with physical disabilities? What about the housebound bedbound ones? The ones need gait trainers walkers wheelchairs? What about the ones who full time users? Or the ones that need power chairs to independently move around? What about the ones crying screaming throwing up from their pain?

What about the disabled that always have a horrible attitude because tired of the disrespect? Tired of having to explain everything about them to everyone even if personal? Tired being told get over it n just educate others?

The disabled ones tired telling people not use certain terms. Tired of being spoken over n for without being thought about or asked. Tired of hearing their communication isn’t valid for ‘xyz’

Y’all support but act very picky about who deserves support and who’s not worthy of it. It’s not support if you pickin n choosing

[teddybearworld]

Question for people who use screen readers or text to speech/audio

When a post on here has lots of emojis, special fonts/text or lots of keysmashes, what is a way to tag those posts so that you guys don't have to sit there listening to nonsense for a minute straight?

Thanks!

[fagtionnow]

you "support mentally ill disabled people" until you see me as out of touch with reality.

you "support mentally ill disabled people" until I spend hours plucking out my hair, and now I'm covered in scabs.

you "support mentally ill disabled people" until I threaten you when I'm upset.

you "support mentally ill disabled people" until I can't even make myself as simple as toast.

you "support mentally ill disabled people" until I smell terrible because I haven't showered in so long.

you "support mentally ill disabled people" until even once I do shower, I still smell bad because I don't have the skills, strength, nor the willpower to clean myself properly.

you "support mentally ill disabled people" until I yell at you and NEED you not to yell back.

you "support mentally ill disabled people" until I throw hard objects against my wall.

you "support mentally ill disabled people" until I'm semi-incontinent.

you "support mentally ill disabled people" until I'm homicidal.

you "support mentally ill disabled people" until I feel no remorse.

you "support mentally ill disabled people" until I bite.

you "support mentally ill disabled people" until I feel no empathy.

you "support mentally ill disabled people" until I try to hit you with my cane during an episode or meltdown.

you "support mentally ill disabled people" until I throw my AAC at you during an episode or meltdown.

At that point I'm either gross, or a bad person.

[sirenium]

For anyone who is semi verbal, nonverbal, or otherwise struggles with speech, please know that there are people who will accept your methods of communication. There are people who won't infantilize you for using AAC, communication cards, making noises instead of words, etc. There are people who won't expect you to pick the mask up again when you stop being so 'talkative'. There are people who don't mind waiting for you to sort your thoughts, and are happy to include you in the conversation.

There are people who accept you as yourself, and I don't just mean toleration.

[chrome-barkz-aac]

i made this instagram post !!! there isn't as big of a community of AAC users on instagram so I thought I would share this on my instagram (@cytochromesea).

EDIT: i got an ask that states that not everyone knows what AAC is which is an oversight on my part, it stands for alternative and augmentative communication!

Image ID:

A light blue background with a rainbow and a cloud and some stars. There is a blue border collie with wings holding an aac tablet that says I love you! Text reads: AAC etiquette. Do’s, Don’ts, and other stuff. By cytochrome sea.

The same background appears in every following slide. Text reads:

AAC is my voice! It is not a toy or accessory

Don’t touch my AAC without my permission

Don’t take my AAC away from me, for any reason (joke, punishment, etc)

Don’t press buttons randomly or flip through my communication cards without permission

How would you like it if I randomly poked you on the mouth and throat (or on your hands if you sign)? It would be unpleasant, so don’t do that to me

Some AAC users can speak sometimes. It is not your business why someone can or cannot talk

Don’t ask questions about why an AAC user cannot speak. 

Do let us communicate however is best for us in that moment

Don’t ask us if or when we will be able to speak verbally. It’s not your business 

Do not value verbal speech more highly than AAC. Any communication is good communication

Some of us never talk, either, and that’s ok! Those of us who can talk sometimes are not better than those of us who can’t. None of us owe you an explanation for our use of AAC.

Don’t look at my screen until I show you. It feels really invasive!

It feels like when someone is looking at your phone screen over your shoulder, so please don’t do this

This applies to low tech AAC as well, don’t look at someone’s cards or letter board until they show you

You have the dignity of forming your thoughts in your head before you say them, whereas my thoughts are all on display. Please afford me the same dignity that you get automatically.

Don’t shame someone for not being able to speak verbally. It makes us feel horrible

We are real people with thoughts and feelings. Please treat us with kindness. 

We are trying our best

Don’t shame someone if their device mispronounces a word. It’s quite literally out of our control.

Other Don’ts. Don’t

Don't Treat an AAC user as childish or stupid for not being able to speak. Our ability to speak does not define our worth

Don't Show frustration at the way someone communicates

Don't Make comments about how fast or slow we communicate

Also don’t…

don't Act surprised when we swear or talk about adult topics like sex, drugs, or violence. We are not pure uwu precious smol beans, we are normal fucking people

don't Assume what is “wrong” with us. There are about a hundred reasons for someone to use AAC and you probably aren’t the expert in any of them.

“OK, so what CAN i do?” im glad you asked! When interacting with an AAC user, DO…

Ask us how we prefer to communicate and support us as you are able

Assume that we are competent

Talk to us with the same respect, tone and vocabulary that you would for any one else

Give us money (this one is a joke)

Understand that AAC grammar isn’t perfect and we are doing our best

Is it rude if…

I can’t understand your device? Not rude! Misunderstandings happen all the time in any conversation, just be patient as you would normally. 

I want to complement your AAC? Not rude!

I ask to see your AAC and understand how it works? This isn’t rude if you are already talking about AAC, but don’t ask random strangers this. They don’t owe you an AAC tour. 

Thank you for listening! This post is for the community! If you are an AAC user, let me know if I missed something in the comments and I will pin it! I hope you are filled with peace and love and I hope something good happens to you today! End ID. 

[tontoemojis]

doodled machine { our AAC device } !!! 🎨

do not use or repost our art ❌️ no no no

[pixierainbows]

Pixie lost a question tumblr post and not sure exactly what was ask . took Pixie so so long time to answer . Weeks of work … So here is answer with no question . so sorry !

A few things about being actually nonverbal ( Never able use mouth words at all , ever … “going nonverbal” is NOT A THING ) .

1- AAC Very slow compare to mouth words . Can take Pixie 10 or more minutes just to give answer to “ hello how are you ?“ Longer word things , like simple blog post , can take weeks to months . people are never that patient , even otherwise good people can just not wait , not without practice .

2- being nonverbal , needing AAC to Communicate all the time , make many things much harder or not possible at all , even with help .

example -

Most medical professionals Pixie have known will not accept communication with AAC device As genuine communication . And ! also will not accept communication from someone else , what is not biological parent , unless AAC user verbally ( not with AAC device ) give permission . Or . personally fills out in writing many forms giving permission . Even then . Is not work every time .

is Same for many many other things . banks and government agencies and schools and businesses and organizations of all sorts .

3- Geting emergency services like ambulance or Police or Firefighter services require speaking . so , need someone else help by calling .

4- many programs for disabled people will not allow access to programs if person cannot *speak* independently . ( Pixie lucky have found some good programs , in big city really help have more programs to choose from )

Pixie also have cognitive disability and moderate to severe language difficulties . but ! even people what just not can speak And not have anything else disabling ( unlike Pixie ) Still need so much more help just because of not able speak ever .

[nemo-bros]

i think lots of people do not realize how long it takes to set up aac (low tech or high tech)

low tech requires lots of printing and cutting and laminating and hole punching and more cutting etc

and high tech requires hours of sitting with device and customizing not just settings but words, folders, layout etc

[five-thousand-loaves-of-bread]

it easy change my voice on AAC.

easier than mouth speak people.

go to setting. go to voices. look, there entire lists. you can try them on like coats in mall. if don’t like them, in press of button you can have something new.

some, can change pitch. can make deeper. can make higher. can make faster. can make slower.

world in your tablet.

it hard change my voice on AAC.

my AAC. is my voice. is identity.

can change with press of button. but not so easy. we have history. my identity entangled with how AAC sound. how i sound.

change voice feel like loss of identity. feel empty. feel lost. feel like line carve in stone, divide me in past and future.

it hard change my voice on AAC.

do speaking people have to choose from limited list of pre synthesized voices? do speaking people run into other speaking people with same. exact. voice as them, same pronounciation errors, same annunciations, same tone, same exclamation?

do speaking people have to compromise within self and share that same voice with other people, a voice that yours but never fully yours?

it hard change my voice on AAC.

mouth speak people. as they age. mature. grow old. switch context. voice naturally changes. voice grows with them.

mine stops. mine frozen in time.

transition from one life stage to another. should i change a voice? to make pallatable for people around me, more professional, more mature, more “taken seriously,” but lose self in process?

it hard change my voice on AAC.

many choices for “standard” (< white) american (< USA) english. many choices for british english. some choices for spanish.

where my diaspora accents? where my languages?

can my friend not speak their mother tongue?

- thank you for give me outlet for voice, but you all that i have

from nonverbal full time aac user

(as in nonverbal all the time)