I Am Currently Working On A Story And I'm So Happy Its So Fun And I Forgot I Somewhat Know How To Draw

im reblogging bc ppl who say that is so stupid, like no i don't like being acutely aware of every noise and texture around me

very fascinated by people who think autism is some hip-happenin’ bandwagon thing to have suddenly when it didn’t ever make me cool in the slightest? it just made me able to hear lightbulbs and have panic attacks over trying to call people on the phone

my school is confusing tee bee ach

SOO today i was listening to music all fine and dandy then its blocked!!! turned out my school blocked sexy from mean girls... i do not understand that bc like my school has some baaad songs unblocked but, that's what I get for being a theatre kid ig

i love u fat cripples, use any mobility aid u need and don’t give a fuck about fatphobic ableists.

we are not just fat and lazy for using mobility aids, we are simply fat and crippled. and we deserve the mobility aids we need.

[this is about fat physically disabled ppl. do not derail.]

what the fart do i post, idk what to post and huhsdafhkhfdksh I don't think everyone wants to hear medical stories/lh

ablebodied ppl will be like “i know you’re in constant excruciating pain but why are u so grumpy” and not hear themselves

(Tw for a VERY brief mention of infantilization)

I want to talk about interacting with AAC users in person, specifically for speaking people.

1. Being an AAC user, I get left behind during conversations a lot because it takes me longer to add in my statement. By the time I'm done, the topic has oftentimes changed and then what I want to say isnt relevant anymore, and sometimes wont even be understood because to everyone else what I just said was out of place and random. This feels really frustrating and sometimes isolating, as well as embarrassing. Please wait for us, we want to converse too.

2. Sometimes when I am not yet done responding, people will watch me and try to guess what I'm going to say. If all I've got down so far is "I already", people might go "I already.. know!" "I already.. saw!" etc. Please stop doing that. Even if you got the idea correct, you might use the wrong words, which frustrates me. And even if you say it all correctly it's still frustrating, imagine if someone tried to guess what you were saying by interrupting you every time you started to talk. It's annoying.

3. Dont comment on what in our folders. If I open a folder to get to another word, and whilst doing that you see a different word in it that's funny or inappropriate or whatever, keep it to yourself. Its annoying. You have acsess to those words, and it isnt treated as weird, so why is it for me?

4. Don't infantilize us. We aren't perpetually children. We are our age. Treat us as if we are a speaking person of our age.

me </3

who else is sick right now

D2& for me

I’d choose D5&

What about you?

Link to post

disability pride ask game

I'm so sleepy but I have persisted anyway bc i am so brave

feel free to reblog, try and send an ask to the person you're reblogging from so the game doesn't die, and absolutely never be pressured to answer anything that feels too personal--this is about/inspiration for what you Want to share about disability and experiences being disabled, not what you feel like you have to! (also: this ask game is PRO SELF DX.)

what disability/ies do you have? (and are they mental, physical, or both?)

how long have you known you're disabled? does that match up with diagnosis?

what, if any, disability aids do you use? (mobility aids, sensory aids, braces, communicative devices, IVs, etc. meds also count here). do you customize them/their containers/outsides?

do you know any disabled people irl? what about online?

if you have multiple disabilities: do they affect each other? how?

what's something good that's come out of being disabled?

what's a struggle you wish more people talked about?

does your disability affect how you experience other parts of your identity? (gender, queerness, culture, even hobbies/life goals you're very passionate about)

how do you measure your energy? (spoons, battery, something else?)

whats something youve come up with or integrated into your life that makes disability easier, besides typical aids?

how would you label your support needs?

what's something (a struggle, a symptom, a weird phenomenon, or even a funny experience) people don't realize about your disability?

whats the most Abled Person Thing someone has said to you?

has there ever been a time where you felt solidarity/community with another disabled person in a situation with you?

what does disability pride mean to you?

free space to talk about whatever disability issue or experience you want !