Due To Being Unable To Know When I'll Be Able To Eat, There Is No Breakfast, Lunch, And Dinner. I Simply

I say shit like "If my memory serves me" knowing damn well it serves the dark lord

"Friends dont look at friends that way" COWARD. I look at my friends with awe in my eyes, my chest is filled with love, im glowing because i get to be near my friends. I look at my friends and i would give them my everything. SO SKILL ISSUE, look at your friends with all the love that you have

Having autism is going to yet another therapist that so obviously has no fucking clue what to do with you. I just had to explain to my therapist that she needs to ask me questions.

There needs to be a simple job where I do the same thing over and over without having to be creative. That has decent working conditions and pays a livable wage

I can always tell when teachers have kids of their own bc I always make them switch from teacher mode to parent mode. Earlier today, my pe teacher was said his normal chill "Have a good one" to my classmate, then I walk by defaulting to my whispery please-don't-yell-at-me voice and he immediately is all like "Yeah ^-^ You have a good day kid :)" like sir u have a toddler don't u.

Shout out to people who are frustrated with their mobility aids:

People who need more supportive aids than they have.

People who need less supportive aids than they have.

People who need a custom mobility aid but can't access it.

People whose family/caretaker(s)/doctor(s) are preventing them from getting best aid for them.

People whose mobility aids are broken and can't be easily fixed or replaced.

People who have the right mobility aid for them but face a lot of inaccessibility.

People with big, noisy, or otherwise attention-grabbing aids that draw unwanted attention.

People whose mobility aids cause pain, fatigue, or other symptom increases that can't be remedied.

It's ok to have mixed or negative feelings about your specific mobility aid or about needing an aid in general. Expressing frustration about your aid isn't being ungrateful or setting back progress in disability acceptance. It's normal to be frustrated when you're being prevented from living the life you want to live.

[Image ID: a banner that says "this post is about physical disability, don't derail" on the first line and "physically abled people don't speak including talking in tags" on the second].

Reblog if you didn’t write My Immortal

We’re going to find the author by process of elimination.

i think bedframes are anti-human devices because how do i jump on my bed like a child without crushing my skull on the ceiling now. what if i wanted to test out my whimsy hello

💙

aac ask game

💙: What kind of aac do you use?

I use writing on paper or typing on my phone and unassisted aac (gestures and noises). Will be getting more soon. I recently became minimally speaking, so I do not currently have many specialized aac devices. I want cards and to try an app.

people with tooth decay aren't bad people. they aren't lazy either. neither are they unclean or irresponsible. tooth decay doesn't make you a bad person. you don't deserve mockery, judgement, or tooth pain for having any. the only thing people with tooth decay deserve is healthcare.