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#visibility disabled
wacklemons · 1 year
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Something I've noticed since I've gotten my diagnosis for fibromyalgia and mobility aids (I noticed it before but its more noticeable to me now that I am more visibility disabled, even though Ive always had noticable disability) is that in first world countries, people are less likely to actually give someone who the "priority seating" is for the seats. Usually people who should 100% be sitting will give up the seats for me which makes me feel bad but I appreciate it.
In the country my family is from (Colombia) people give the people who need seats no matter what, even if there are other seats for us to sit in. People also dont use things made for disabled people there, unlike in first world countries.
In my school, the elevator is for disabled people only but able bodied people go on it to skip class or to not use the stairs. I understand that stairs suck but the elevator just isnt for them, there have been people who started to mock the disabled people in the elevator, some who have called us cr*pple, and adults telling the actual disabled people to get off instead of the able bodied people who arent even allowed on it.
People act like being disabled makes life easier because people will "give you things" but people don't. People take advantage of whats for us and then berate us for telling them they can't use the things or to let us have what is for us. We are not assholes because we are disabled, we are mad at able bodied people taking advantage of whats ours and acting like we don't exist. Let us have our equitity.
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satellites-halo · 6 months
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yeah you're "punk" but are you normal about deformed people?
Edit: reblogs are off because my notes have been filled with this post for months. the correct term is 'people with limb/facial differences' and this post was originally about the cripplepunk movement not punk as a whole
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zebulontheplanet · 8 months
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Just a reminder that people who still live with their parents as adults deserve respect and for you to stop being ableist. There are multiple reasons someone could still live with their parents! From invisible to visible disabilities, finance issues, and more!
Stop using the “well they’re gonna turn into a creep living in their parents basement” punchline! It’s disgusting. STOP. BEING. ABLEIST. STOP. FORGETTING. THE. POOR.
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balthazarslostlibrary · 7 months
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Dan Piraro, Bizarro Comics 2006
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theamphibianmen · 9 months
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"low support needs disabled people are often not believed to have a disability at all and therefore struggle to get accommodations."
"high support needs disabled people's accommodations are often seen as 'too much' and therefore are not met."
"neurodivergent people's needs are often dismissed because nothing is physically wrong with them."
"physically disabled people people often cannot physically access buildings and people refuse to do anything about it."
"invisibly disabled people are seen as lazy by society."
"visibly disabled people are ostracized from society."
IT'S ALMOST LIKE THERE'S NO SUCH THING AS A SOCIALLY ACCEPTABLE DISABILITY
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kaibascorpse · 3 months
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some of you people are so obsessed with having an acceptable group to ‘punch up’ at that you would rather pretend a marginalized group are Basically The Oppressors™ than listen to their valid criticisms about the fact that ‘punching up’ very rarely hits the intended target, and the majority of the actual damage of that act is suffered by fellow marginalized people in your own community. there is a significant difference between venting frustrations about privileged groups and just outright attacking anyone who (you assume) experiences that axis of privilege regardless of - and in many cases outright denying - their actual lived experiences. it goes far beyond just ‘venting frustrations’ when what you’re really doing is trying to find a moral justification to bully people you don’t like, and when your own desire for catharsis and moral superiority leads to ignoring the voices of the vulnerable people you hurt. you’re not ‘punching up’ - you just like punching people for the sake of punching.
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sneakygreenbean · 11 months
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personal observations made by a new cane user:
you do not need to be in constant pain to own a cane.
folding canes have a clasp or band to keep them folded. losing the band is a pain in the ass.
you will get dirty looks
it does not matter what age you are. you will get dirty looks.
you have to hold it in the opposite hand as the disabled leg. this is fortunate, as I am right handed, so i hold it in my left hand to support my right leg.
people will try to steal your cane from you.
when standing still, I hold it in my right hand unless i need to do something right handedly. this does not work as well as i thought it would.
being visibly physically disabled is difficult. having a mobility aid will help with pain and movement, but some people don't get them because visible disability is treated with disgust.
if someone meets you for the first time, and you don't have your cane, then they will like you more, but they will not believe you are actually disabled.
if someone meets you for the first time, and you have your cane, they will not treat you the same.
the majority of other cane and mobility aid users I have met are homeless. I live close to a big city.
People do not want to see you being disabled.
you will not hear of the benefits of using a cane from anyone who does not use a cane.
no one will prepare you for the world of being visibly physically disabled. however bad you think we have it is usually not from the disability at all. I can deal with pain and I can deal with an indisposed left hand.
the hardest part of being disabled is the fact that no one will care until you make them care.
the disabled seats on trains are a suggestion
the disabled seats on buses are a suggestion.
you will have a different experience with using a cane than I have had.
your hand will become tired. you are using it as a leg.
your cane is legally a part of your body. this will not stop some people.
you are not your disability. but it will affect you.
i love you
theres always an invisible someone who has it worse. that person will not be affected or offended by your use of a cane. take the damn ibuprofen. put the folded cane in your bag. ask your friends for help. gd knows they need help sometimes too.
you will have to learn that things will be impossible to you. you may not run as fast anymore. you may not become a skater, like you always wanted to be. you may be left behind when everyone else runs ahead.
you deserve better.
your cane handle gets dirty. wash it.
some days pain is worse. some days you will feel it the moment you wake up.
no one deserves pain. the human condition is not to suffer. we deserve better. we deserve to be loved and not tolerated. we deserve to be seen better than from the corners of eyes. we deserve to be heard better than an afterthought at a meeting.
be quick to care for yourself. I love you.
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soggedboytroutanti · 3 months
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hey guys. Reminder. Disabled people who played a hand in and/or caused their disability still dont deserve any pain it causes them
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isa-ah · 2 years
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that’s what the aids are for!
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mavigator · 5 months
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i talked about it a little bit already but i have things to say about it. for context, i was born with amniotic band syndrome. the amniotic band wrapped around my left wrist in utero and stunted the growth of my hand. i was born with about half a palm, four nubs for fingers, and a twisted half of a thumb. i can open and close my thumb and pinkie joint like a claw.
yesterday at work i had a shift in the room with 5-10 year old kids. i had my left hand hidden in my sleeve (a bad habit of mine). a kid asked if he could see my hand, and even though internally i was debating running into traffic, i said “sure you can” and showed him my hands. he stared for a moment, looking disturbed, and then said “i don’t want to look at that anymore”. that hurt to hear, but i understand that kids are new to the world and he probably didn’t mean it out of malice. i put my hand away again, told him that it was okay, and that i was just born that way.
he then went on to talk about how he knows a kid with a similar hand to mine and called it “ugly”. i told him that wasn’t a very kind thing to say and that he wouldn’t feel good if someone said that to him, and he replied that no one would say that to him—because he has “normal hands”, and he’s glad he does because otherwise he’d be “ugly”. i tried to talk with him for a bit about how everybody is born differently, but he just started talking about a girl he knows with a “messed up face” and pulled on his face to make it look droopy. i went on some more about how it wasn’t very kind to talk about people that way, but the conversation moved on to something else.
i’ve told my supervisors about it and they’re going to have a talk with his mom. what i wanted to say is this: i’m genuinely not upset with the kid. kids are young and naturally curious, and he clearly simply hasn’t been taught about disabled people and kind ways to speak to/about others. which is why i am upset with his parent(s). i know he’s encountered visibly deformed/disabled people before (he said so himself!), yet his parent(s) clearly haven’t had any kind of discussion with him about proper language and behavior. i knew from birth that some people were just different than others, but my parents still made a point to assert to be kind to and accepting of others. i wonder if adults in his life are the type of people to hush him and usher him away when he points out someone in a wheelchair. that kind of thing doesn’t teach politeness. it tells children that disabled people are an Other than can’t be acknowledged or spoken about; which, to a child, means disability must be something bad.
i’m lucky enough that this was a relatively mild incident, and that i’m a grownup with thicker skin. i’m worried about the other kids he mentioned to me. has he been talking to them this way? when i was a kid, i had other kids scream, cry, and run away at the sight of my hand. or follow me around pointing at me and laughing at me. or tell me i couldn’t do something because i was ugly or incapable or whatever. one time a girl at an arcade climbed to the top of the skeeball machine, pointed at me, and screamed at me to put my hand away and wouldn’t stop crying until she couldn’t see me anymore. another time, a kid saw my hand, screamed at the top of her lungs, and ran into my friend’s arms, crying hysterically about how i was scaring her. that second incident made me cry so hard i threw up when i got home. i can kind of laugh it off now, but having people react to me that way as a child is something i’m still getting over. why do you think i have a habit of keeping my hand in my sleeve? it just irritates me to see children that have clearly not been taught basic manners and kindness—their parents Clearly missed something pretty important .
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holierthanth0u · 3 months
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im kinda tired of the assumption that physical disability = visible, and non-physical disability = invisible. it is not that simple and it certainly aint the case for me.
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Even if you, personally, don't hate Discord's new UI, I am begging ya'll to still send them the following feedback:
"The changes made to Dark Mode are an accessibility issue due to the lack of a low contrast option for those who need it."
The previous dark gray was never ideal, tbh, but it was still worlds better than what we have now. As someone who can feasibly get by with the new dark mode but vastly prefers low contrast, and as someone who knows people who do need low contrast -- please tell them about this problem.
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valcaira · 10 months
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Look I get that we all want to relate to one another. I really do. But seeing people on my post about how shitty it is to exist as a visibly deformed & disabled person in public say things like "that's why i don't stim in public" or "that's why i'm scared to bring my cane in public" is just... You're missing the point.
Some of us cannot mask our disabilities. You can simply not stim if you can supress it in the first place. You can leave your cane at home if you're doing that already in the first place. A knee brace doesn't make you look like a "freak". You do appear abled otherwise.
I cannot. Many people I know cannot. I can't just "hide" my deformities and abnormal gait or convulsions to appear abled. I *need* my crutches everywhere I go. I can't supress my tics. Full-time wheelchair users exist. High support needs autistics exist. Schizospecs who cannot mask exist. People with William's Sydrome, Down's Syndrome and various obvious deformities exist. Little people. People with severe chemical burns or otherwise or scarring. People with Parkinson's, Tourette's, Huntington's, Cerebral Palsy, every disabled person who looks "abnormal".
We can't just "turn it off" like you. People WILL stare at us. Point their fingers at us. We have no power. They used to put us into freakshows. Not you. Not you who can hide your disability to "appear normal". That post was not for you to "relate to". I and many people are sick of many invisibly disabled people claiming they "want to look disabled" so they'd be "taken more seriously". It's not an invitation of you to declare you leaving your mobility aid at home or shit like that. It's not the damn same.
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echo-bleu · 4 months
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Eärendil the Mariner
Who deserves a pirate outfit more than Eärendil?
The background is largely inspired by one of Philip Sue's paintings. It was fun to draw a flat earth!
In other news, I love drawing ships but that was the worst angle possible to figure out. In my head, the Silmaril is at the prow in some kind of glass/mirror lantern that amplifies its light.
I wanted him to look soft, and little wry maybe, rather than fierce. I'm sure he's fierce aplenty but I mostly headcanon him as tired. His fate breaks my heart. Also, it doesn't really show here but my Eärendil is blind from overexposure to the Silmaril (and half-human fragile eyes).
I always waver between giving him locs or a shorter Mannish haircut, but his hair is really too kinky for the shoulder-length, Aragorn-style cut, so locs it is!
IDs in alt text.
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elysianmadness · 1 month
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Happy lesbian visibility week/day to every lesbian around the world! I hope you're going to have a wonderful week, wherever you are. Your lesbianism is perfect and needed in the world. In this household, we love and appreciate the diversity of the lesbian experience <3
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cy-cyborg · 9 months
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This is just a not-so friendly reminder to non-disabled people, especially authors, people in fandoms or in media analysis circles: Cripple/crippled is not just a fancy way of faying "badly injured". it's not an adjective you can just throw in to spice up your sentence because you used "injured" or "disabled" too many times in that paragraph, or because you feel like it gives your writing some extra "oomph".
Cripple is a slur.
A slur the physically disabled community has been asking people not to use for DECADES, since at least the 1970's (50 years). It's a slur with centuries of abuse behind it, centuries of being used to justify physically disabled people as less-than, centuries of demonisation, mistreatment, ostracization, and murder.
Some people within the physical disability community are reclaiming it, that's where movements like cripplepunk (also known as crip-punk or C-punk) come from. That's fine, I'm not talking about that. I love the cripplepunk movement and everything it stands for: being unapologetic about our disabilities and not changing ourselves for the comfort or convenience of able-bodied folks. But the people who use it in that context understand the history of the word, they know how it was used to hurt us, and they understand that not everyone in the physically disabled community is comfortable with the use of the word, especially those who were around when someone being labelled as "crippled" was seen as a valid reason to treat them as less than human. They understand the impact of the word.
But If you, as an able bodied person, casually uses "cripple" in your work, at best you are showing your disabled audience that you haven't been listening to us, at worst, you show you don't care about weather we feel safe in the spaces you have created.
And for able-bodied authors specifically, even if your character is physically disabled, I'd still recommend avoiding it unless you're prepared to do a LOT of sensitivity readings from multiple sensitivity readers. I've been physically disabled since I was 1 year old, I learned to walk for the first time in prosthetics and have been using a wheelchair since I was in school, I have no memory of life as an able-bodied person, and even I don't feel comfortable using the word cripple in my work.
It's a loaded word, with a lot of implications and a LOT of very dark, and for some people, very recent history. It's not a sentence enhancer to just throw in willy-nilly. Please.
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