ableism is a disease, but luckily there’s a cure:
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ableism is a disease, but luckily there’s a cure:
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sometimes people dont really understand that having schizophrenia doesn’t permalock me as an angsty 13 year old evanescence fan
moved into my dorm and my crippled ass has to climb up and down a rickety ladder to get in and out of bed smh
why is it so much work i just have to pee
ice cold take but if you have to pay for accessibility features it is not in fact accessible
moved into my dorm and my crippled ass has to climb up and down a rickety ladder to get in and out of bed smh
pet peeve of the day i can’t stand when abled people get fairly minor temporary injuries and then start throwing around the word cripple like it’s theirs
btw the abled ND =/= cripple punk debate isn't "slur discourse". it isnt us big mean cripples gatekeeping others from the community for no reason. its about respecting Tai, the creator's wishes on the cripple punk moment being by and for physically disabled people only. there are other similar movements out there (neuropunk and madpunk) that work towards the same goals but for mentally disabled people. please use them.
Does it count for chronic pain? My body is perfectly capable but it hurts the whole time.
i mean. there’s nuance of course but i’d say if your body is in pain the whole time it’s not really able-bodied. abled means capable and without restriction or difficulty
we should not be prescribing moral qualities to how much a person sleeps per day or struggles to be mentally healthy
sure you have "neurospicy accomodations" (stim toys and slime) at your support group meeting but are masks required. is it wheelchair accessible? is the lighting harsh or flickering? is there a place to go if you're upset or overstimulated? is there a clear schedule? does anyone in the group speak sign language? could a nonverbal person participate? are there multiple options for activities? is there music? is it loud? is there food? how many options are there? are there common allergens in it? are they clearly labelled? are there flashing lights? can you attend virtually? are hallways and pathways clear? are there accessible bathrooms? do they have a sharps box? do they have space for someone to transfer from a wheelchair to a toilet? do they have space for a caregiver or support worker? are there enough places to sit down? is there enough space for everyone to be without crowding? can people opt-out of planned activities? et cetera...
i can't get over how evil it is that "gap in your resume" is considered a valid reason to not hire someone like "hmmm sorry you weren't working constantly every day of your life we need people who do nothing but work until they drop dead for us we just don't think you're right for the job" fuck youuuu
workplaces should have to legally provide unlimited paid sick leave available immediately upon hire. the limits that companies that even provide paid sick leave put on it is so fucked up. no one can control when they get sick, how often they get sick, or how long they are sick for, and they shouldn't have to suffer for the transgression of being ill.
"oh, but some people might take advantage of that and just stay home all the time and get paid for it!" if there is really a statistically relevant amount of people you have hired staying home on paid sick leave for months or years on end, perhaps your workplace sucks to be at, and you need to change.
give them reasons to come in to work. make it safer and easier to do their jobs. give them work that they can get invested in and talk to them about what that looks like. make sure you aren't overloading them with too much work or making unreasonable demands. pay them an amount that makes the work worth doing to them. actually form a working relationship with your employees instead of treating them like infinitely exploitable wage slaves.
only allowing your workers to accrew "2 hours a week of sick time starting after 6 weeks of employment" or some shit just doesn't match the reality of how sickness or human health works
a person online: i hate it when adults act like childish little freaks in public, smh. you’re an adult, you should be able to order your own food without help. get over yourself. also, why are some people, like, waaaaaaay too into the stuff that they like? omg, and the people who CLEARLY can’t even have one (1) normal conversation without acting Weird??? it’s embarrassing, u guys are embarrassing, get help
the same person five seconds later: we gotta remember to love and support the autistic community u guys <3
you know, in hindsight this reminds me of something
when i’m at work, people get mad at me for not hearing them the first few times. like, openly agitated. they’ll assume that i’m stupid, or rude, or careless. sometimes they will indirectly chastise me for ‘not paying attention.’ at which point i say “i’m sorry, i’m hard of hearing. you were on my right side and i’m severely deaf in that ear,” and they go “oh my god i’m so sorry i didn’t know.”
yeah. you didn’t, did you? the only available information you had about me was… that i didn’t hear you say something. the thing you hated enough to comment on was that i couldn’t hear you. you don’t get to backpedal once you find out that i have can’t-hear-well disease. i shouldn’t need to present a diagnosis to expect decency from you
if you attach negative characteristics to “didn’t hear what you said,” that will affect how you treat d/Deaf and hard of hearing people. if you attach negative characteristics like “weird and childish” to utterly harmless and well established autistic traits like “doesn’t make eye contact,” that will affect how you treat autistic people. it’s not rocket science
honestly test scores being such a high percentage of overall course grades is just setting disabled students and people with test anxiety up to fail. like no amount of studying and preparation can make your memory any better or your anxiety any lower when it’s just how your brain works. i could know all of the course content like the back of my hand and still fail the exam because i can’t perform well on tests. i really wish my uni and professors would realize this
Imagine my shock as a neurodivergent teen when I first realized that using large vocabulary and eloquent speech doesn't make you less likely to be misinterpreted, rather it adds an entirely new layer of misinterpretation I had never even realized existed in the form of people thinking you're being snobbish or condescending when you're just trying to be specific
“invisible disabilities” in my experience aren’t actually that invisible if you spend more than a few moments interacting with someone who has one. the term invisible disability is meant to describe people who aren’t perceived as disabled upon first glance. it’s not an excuse for abled people to ignore symptoms or struggles because they think the disability is supposed to just not exist because it’s not visible.
also in the spirit of disability month i want to address those “well why don’t you just ask for help” comments with a little tidbit of my own, where i asked for accommodations at my college (that had already been met the previous semester with proper documentation and diagnostic papers, mind you) and was abruptly met with a simple, “i (student accessibility rep) don’t feel that you (disabled student in need of accessibility) need these accommodations and im not going to enable your procrastination (read: uncontrollable brain chemistry deficit)”.
so why don’t i just ask for help? simple. because every time i do i’m met with more ignorance and refusal. every disabled person has been or will be denied fundamental access and equity at some point in their life. it becomes an expectation. accessibility and assistance is not the norm for us; it’s a surprise when we get actual help to the extent we require it. we are being actively disabled by our environments and the systems in place built for the abled. so no, it is not as simple as asking for help. we have to fight tooth and nail every day to get even the barest minimum and i’d really appreciate it if abled people stopped acting like any of this were simple or easy.
It’s worth noting that Kenneth spent the entire episode making the game (and the subsequent fight) as inclusive as possible for JJ and his disabled friends (all of whom were played by disabled actors/actresses).
i feel like we dont talk enough about how distressing and disturbing memory loss issues are. forgetting what you were talking about halfway through a sentence, putting something down and instantly forgetting where you put it. having to reread one paragraph over and over again because by the time youve moved onto the next sentence you dont remember what the one before it said. always doubting if your memories of things are real, not being able to remember important life events.
its so incredibly scary, it feels like your mind is constantly playing tricks on you and you start to doubt whats real and what isnt.
“i forgot” is treated like a lazy excuse when it’s genuinely such a big issue for so many people.