Ableism Mention - Tumblr Posts

Hi guys! Here’s some advice from a cane user on how to spot a fake cane user/disability faker!

YOU CANT

You can not spot a “fake disabled” cane user. You can not know if someone’s “really disabled”, much less by just looking at them. Here are some common misconceptions.

“Cane users always need their canes. If they walk without it or put it away when it’s inconvenient, they’re faking”: WRONG! Many cane users are what we call “ambulatory” cane users. This means they don’t always need their canes to walk. I’m an ambulatory cane user, and I experience really horrible leg pain on the daily. However, I don’t always use my cane, and when I don’t need to walk or stand a lot in a certain place I don’t use it. And when I do use it, I may lift it off the ground or carry it in places that are sandy, gravelly, or otherwise hinder my cane.

“Cane users walk abnormally without their canes, someone who walks normally without their cane is faking”: WRONG! Many ambulatory cane users can walk in a way that seems “normal”. This doesn’t mean they’re not in pain, or not “really disabled”. This just means that their condition doesn’t cause a noticeable difference in walking, and likely manifests in a different way.

“Cane users always need their cane, someone who doesn’t use their cane at home is faking”: WRONG! Cane users may not use their canes at home, because at home they may be able to do things like sit down wherever and whenever, regain more spoons, and use other mobility aids. Additionally, some ambulatory cane users only need or use their canes when they are doing something physically taxing, like going on a hike or standing in a long line.

“My cane user friend told me this person looks like they’re faking, so it must be true”: WRONG! Being a cane user doesn’t immediately make you an expert on all different conditions and experiences. Your friend does not know the random cane user walking down the street, they are going off looks and stereotypes. Disabled people are not immune to being ableist.

“They enjoy their cane too much/they’re too happy/they decorate their cane, so they can’t actually be in enough pain to need a cane” WRONG! We’re people like everyone else, and we experience positive emotions too, even if we go through a lot of pain. To me, customizing my cane is like getting a tattoo or putting streaks in my hair, it’s a way of self expression. And we deserve to be able to talk openly about our full experience, which include the parts we’re neutral or happy about.

“They’re one of those cringey teenagers who name themselves arson and like dsmp, so they’re probably faking” WRONG! Do I even have to explain why saying someone isn’t disabled because of their name and interests is messed up and also stupid? Or did you already know that and just wanted to make fun of a disabled teenager?

“They’re too young to be using a cane, so they must be faking” WRONG! there are lots of disabilities or injuries that can cause young people to need a mobility aid. For example, I use a cane for my fibromyalgia.

“They only use it in private places, and never in places where people recognize them, so they must be faking” WRONG! In a world where anyone can just randomly take out their phone, take a picture of a cane user, and post them online to be made fun of, it can be stressful to use a cane in public areas. Also, they may not want people to ask questions, or they may feel embarrassed about it.

“I saw them switch hands, so they must be faking” WRONG! There are different reasons a cane used might do this, but I’m going to use my experience as an example. My fibromyalgia is not consistent. Sometimes one leg hurts more then the other. But as I said, fibromyalgia is inconsistent, and sometimes my other leg will start to hurt more or need more support, which is when I switch hands. And when both my legs hurt equally, I may switch my hand if it’s getting too sore.

“They told me they feel like they’re faking when they use their cane, doesn’t that mean they don’t really need it?” WRONG! Imposter syndrome is strong in a lot of disabled people, especially when for a lot of our lives we were told by doctors that we were fine and just being dramatic. Anxiety is also comorbid with a lot of physically disabilities, which only strengthens this. To add to this, something that I’ve felt and seen other disabled people talk about it, when their disability aid lessens the pain, they start thinking “well I’m not in that much pain so I don’t really need it” even though the reason they’re not in that much pain is because of the aid. I know it seems dumb, but imposter syndrome can be that strong and affects disabled people a lot.

“They don’t have a diagnosis, so they must be faking” WRONG! First of all, diagnoses are expensive. On their own they’re often already expensive, but counting the tons of tests you have to take to confirm the diagnosis? Absolutely ludicrous. Some may also choose not to get a diagnosis, so that they don’t have to deal with the prejudice and setbacks of being diagnosed. Also, some people use a cane for injuries, and for stress or fatigue related pains.

These are only a few of the things I commonly hear from fakeclaimers, and I wanted to just put out a reminder that fakeclaiming hurts the disabled community much, much more than it does ableists. Next time you see someone with a cane switch hands, or someone with a wheelchair stand up, or someone with crutches put them down, before you immediately call them out to a friend, take a picture, or write a post: does your fakeclaim rely on stereotypes? Are your reasons things that apply to ambulatory aid users?

If so, just stop. Be mindful. Please.

the thing that gets me the most about ableism against pd’s is that ppl will be like “these disorders make you an ASSHOLE!!!!” and then turn around and pretend that other disorders can’t and don’t make you act shitty.

depression and anxiety can make you irritable and snappy. they can cause you to refuse to listen to people and to be distant and withdrawn. they can cause you to seem angry, bitchy, rude, uncaring, etc.

ptsd causes an array of difficulties in forming meaningful relationships. it pretty much shakes up your entire worldview and sense of self a lot of the time. ptsd can cause you to get angry often. it can cause you to yell and scream. it can cause you to withdraw from others, run away, or cut them out. it can cause general changes in demeanor and more cynical worldviews. it can make you seem grouchy, negative, explosive, impolite, difficult, needy, controlling, etc.

and yet when people with personality disorders have symptoms of that nature, suddenly we are irredeemable monsters. when it’s npd, bpd, hpd, or aspd instead of ptsd or depression and anxiety, people suddenly and magically lose the ability to be understanding.

mental illness is an explanation, not an excuse. i firmly believe that. hurting others is never justified simply because you have any disorder.

but if you can be patient with people who have depression, anxiety, ptsd, ocd, or any other more well understood mental illness, you can be patient with us.

A thought I had about Ghetsis: Even though he developed things like NPD and bipolar from his own abusive father, I don't think he even knew that NPD and bipolar exist. His family didn't educate him on mental health at all and what little they did know about mental illness (specifically anxiety and depression) they told him it was just a bunch of made up crap...

This is how this shit gets perpetuated from generation to generation for real. Ghetsis didn't tell N anything about the mental illnesses he had and didn't give him access to any of that kind of information in general. He just let him suffer all of these unknown and terrifying symptoms like narcissistic crashes and autistic meltdowns with no explanation or way out. Left N wondering what was "wrong" with him with zero ability to find closure about it. It was only when N got out from under his thumb and finally learned the vocabulary to identify his illnesses that he felt that this cycle was broken. And he is determined that the cycles of both abuse and ignorance will end with him.

Ableism in Subtitles

Something that really pisses me off is the litany of ableist issues found in subtitles. So, let's talk about 3 huge issues that need to stop.

Subtitles should never ever say [Speaking -language-]

When a hearing person is watching a TV show, or a stream, if someone starts speaking another language, if that hearing person knows that language, they will get to know what the person said, regardless of if the average viewer knows that foreign language.

Deaf and HOH viewers deserve the same opportunity, and to rob them of that opportunity by putting [speaking -language-] in the subtitles is ableist.

Every word spoken in a show or movie, unless given translated subtitles in the uncaptioned version of the show or movie, should have every word captioned exactly as it's spoken. If someone starts speaking Spanish, the words spoken in Spanish should be subtitled in Spanish. If someone starts speaking German, the words spoken in German should be subtitled in German.

When a show or movie is created, if you want a character to speak a foreign language, you get an actor who can speak that language. When you hire someone to transcribe a show into subtitles, your hire someone who can speak the languages spoken in the show, or you have them mark points where a foreign language speaker will need to assist and then have someone who speaks that language add in the parts that the transcriptionist can't.

Subtitles should never be cut short for convenience

This is something I see constantly. Shows and movies will frequently cut out words or even large chunks of a sentence from the subtitles to make the subtitles shorter.

When you remove descriptive words, parts of a sentence, or even whole sentences to cut down on the amount of subtitles in a given segment, you are completely changing the attitude, mood, and expression of those sentences. You can completely ruin all of the implicit feelings in a sentence if you remove words that show feelings or the way a person phrases things.

It is not your moral right, as a company or transcriptionist, to decide that deaf or HOH viewers shouldn't get the original phrasing.

I am not deaf or HOH. I have APD and have to use subtitles to keep up with what's being said, or I won't process it fast enough. Because of that, I get to see all of the ways subtitles deviate from the original wording all the time. This isn't an issue that just happens here and there. It happens in pretty much every episode of every show I've watched. And it's unacceptable.

Even if we ignore the way this impacts the intent of a sentence, this is ableist by its nature. When subtitles are made, they are made to fill the gap in a deaf or HOH person's TV experience. When you don't accurately fill that gap, or fill it partway, or half ass it, you are cutting corners on a disability aid. It's like if you sold someone a wheelchair with the wheels not pumped with enough air, or giving someone a hearing aid with damaged battery capacity.

When deaf or HOH people watch TV or movies and they use subtitles, they are relying on those subtitles to give them the most accurate wording possible. So why are companies directing or allowing their transcriptionists to half ass or cut down their subtitles? Every piece of media should be having its subtitles checked for accuracy before they're approved, and subtitles that cut corners should be amended before a show with subtitles is published or aired.

Subtitles should never censor words that aren't censored in audio

If a show or movie has swearing in it, of any kind, the subtitles should accurately depict what is happening audibly. If the audio has swear words censored, the subtitles should depict the noise - or lack thereof - that is used to censor the word. Subtitles should never be censored when the audio isn't.

Not only does this touch on the same issue from the last section, it's also ableist in another way. Not only are you giving deaf and HOH people a different experience than hearing people, you're also infantilizing them by disallowing them from hearing swear words that hearing viewers can hear.

Deaf and HOH adults are not children. They have just as much right to read the word "fuck" as a hearing person does to hear it. Censoring subtitles is disrespectful, ableist, and infantilizing and it needs to stop.

Make a change

I'm not familiar with the details of the ADA and how it regards subtitles, but if anyone would like to work with me to do something about this, I would really like to fight for subtitles to have more regulation.

If the ADA prohibits inaccurate subtitles, we should be reporting companies like Netflix who constantly provide inaccurate subtitles. If it doesn't, we should be fighting to amend the ADA to include regulations for subtitle accuracy.

Anyone who's researched this before or who knows more about it than I do, please tell me what you know or give me some sources I can look into myself. I would research from scratch but I'm disabled and don't have a lot of spoons for it, which is why I'd like to work together with others.

//ableism mention tw

ok just gonna say something really quick: i absolutely hate Abe's characterisation in the reboot of Clone High because it is nothing like how he acted in season 1 and it just. isn't funny. they've turned this good-intentioned but flawed loser kid who just wants to be like the original Abraham Lincoln but doesn't know how to, into a self-centered and arrogant asshole who literally almost said a horrible ableist slur twice in the first episode. like. i'm being serious, he almost says the R-slur twice in the same minute and i dunno about you but i really don't find it very funny when a) the only "joke" behind it is "oh look at how bad Abe is compared to the more progressive sensitivities of the new generation of clones, isn't he just terrible", and b) they felt the need to completely rewrite a pre-existing character that fans are already attached to to do something against his own morals for the sake of a shitty joke, and c) TOPHER WAS RIGHT THERE!!! isn't he supposed to be the asshole or am i missing something?? like...

i'm not saying you can't have "edgy" or "dark" comedy or whatever, but personally, i don't find it very funny when a character that actually means quite a lot to me and is one of my favourites is twisted and rewritten into an arrogant asshole in an apparent attempt to appeal to the people who hate Abe for his flaws in the original show. especially when he's rewritten to be someone who would say a slur that's literally been used against my fellow disabled peers, myself included. it just feels... wrong. it actually hurts a lot to see a character i once loved and found to be one of the funniest and most important characters in the show be turned into an arrogant dick, with barely any thought or meaning put into him. i don't like what they did with the rest of the OG cast as well (such as Joan making a complete 180 in her entire character, JFK's character assassination, the removal of Gandhi, Cleo barely being in it etc.), but to me, they did Abe the dirtiest in this season and i'm really disappointed that one of my favourite shows had to continue like this :(

hell o do any other autistic people dislike the term 'meltdown'? for me, the word has a lot of negative connotations because it feels like i'm being degraded and referred to as an uncontrollable tantruming child. i think i have a lot of trauma associated with the word because every time it's been used about me, it's been from teachers who really should not have been around autistic children at all, using it to describe a kid they did not understand, a kid they only saw as bratty, unreasonable, stupid and purposely hard to deal with. it just makes me feel icky and it feels really infantilising to have a term that's usually associated with bratty kids be used to describe a hard-to-understand, unique and painful inner turmoil caused by sensory distress. but that's just my experience.

you know what? let's put a poll here for funsies because i'm genuinely interested in seeing what the people who come across this post think about the word!!

wish all cane users a very permission to beat up ableists with your cane

Hi guys! Here’s some advice from a cane user on how to spot a fake cane user/disability faker!

YOU CANT

You can not spot a “fake disabled” cane user. You can not know if someone’s “really disabled”, much less by just looking at them. Here are some common misconceptions.

“Cane users always need their canes. If they walk without it or put it away when it’s inconvenient, they’re faking”: WRONG! Many cane users are what we call “ambulatory” cane users. This means they don’t always need their canes to walk. I’m an ambulatory cane user, and I experience really horrible leg pain on the daily. However, I don’t always use my cane, and when I don’t need to walk or stand a lot in a certain place I don’t use it. And when I do use it, I may lift it off the ground or carry it in places that are sandy, gravelly, or otherwise hinder my cane.

“Cane users walk abnormally without their canes, someone who walks normally without their cane is faking”: WRONG! Many ambulatory cane users can walk in a way that seems “normal”. This doesn’t mean they’re not in pain, or not “really disabled”. This just means that their condition doesn’t cause a noticeable difference in walking, and likely manifests in a different way.

“Cane users always need their cane, someone who doesn’t use their cane at home is faking”: WRONG! Cane users may not use their canes at home, because at home they may be able to do things like sit down wherever and whenever, regain more spoons, and use other mobility aids. Additionally, some ambulatory cane users only need or use their canes when they are doing something physically taxing, like going on a hike or standing in a long line.

“My cane user friend told me this person looks like they’re faking, so it must be true”: WRONG! Being a cane user doesn’t immediately make you an expert on all different conditions and experiences. Your friend does not know the random cane user walking down the street, they are going off looks and stereotypes. Disabled people are not immune to being ableist.

“They enjoy their cane too much/they’re too happy/they decorate their cane, so they can’t actually be in enough pain to need a cane” WRONG! We’re people like everyone else, and we experience positive emotions too, even if we go through a lot of pain. To me, customizing my cane is like getting a tattoo or putting streaks in my hair, it’s a way of self expression. And we deserve to be able to talk openly about our full experience, which include the parts we’re neutral or happy about.

“They’re one of those cringey teenagers who name themselves arson and like dsmp, so they’re probably faking” WRONG! Do I even have to explain why saying someone isn’t disabled because of their name and interests is messed up and also stupid? Or did you already know that and just wanted to make fun of a disabled teenager?

“They’re too young to be using a cane, so they must be faking” WRONG! there are lots of disabilities or injuries that can cause young people to need a mobility aid. For example, I use a cane for my fibromyalgia.

“They only use it in private places, and never in places where people recognize them, so they must be faking” WRONG! In a world where anyone can just randomly take out their phone, take a picture of a cane user, and post them online to be made fun of, it can be stressful to use a cane in public areas. Also, they may not want people to ask questions, or they may feel embarrassed about it.

“I saw them switch hands, so they must be faking” WRONG! There are different reasons a cane used might do this, but I’m going to use my experience as an example. My fibromyalgia is not consistent. Sometimes one leg hurts more then the other. But as I said, fibromyalgia is inconsistent, and sometimes my other leg will start to hurt more or need more support, which is when I switch hands. And when both my legs hurt equally, I may switch my hand if it’s getting too sore.

“They told me they feel like they’re faking when they use their cane, doesn’t that mean they don’t really need it?” WRONG! Imposter syndrome is strong in a lot of disabled people, especially when for a lot of our lives we were told by doctors that we were fine and just being dramatic. Anxiety is also comorbid with a lot of physically disabilities, which only strengthens this. To add to this, something that I’ve felt and seen other disabled people talk about it, when their disability aid lessens the pain, they start thinking “well I’m not in that much pain so I don’t really need it” even though the reason they’re not in that much pain is because of the aid. I know it seems dumb, but imposter syndrome can be that strong and affects disabled people a lot.

“They don’t have a diagnosis, so they must be faking” WRONG! First of all, diagnoses are expensive. On their own they’re often already expensive, but counting the tons of tests you have to take to confirm the diagnosis? Absolutely ludicrous. Some may also choose not to get a diagnosis, so that they don’t have to deal with the prejudice and setbacks of being diagnosed. Also, some people use a cane for injuries, and for stress or fatigue related pains.

These are only a few of the things I commonly hear from fakeclaimers, and I wanted to just put out a reminder that fakeclaiming hurts the disabled community much, much more than it does ableists. Next time you see someone with a cane switch hands, or someone with a wheelchair stand up, or someone with crutches put them down, before you immediately call them out to a friend, take a picture, or write a post: does your fakeclaim rely on stereotypes? Are your reasons things that apply to ambulatory aid users?

If so, just stop. Be mindful. Please.

With his relentless, manipulative cruelty, his obsessive tendency make people live out the tragic narratives he's imagined for them, his ableism towards a wheelchair-bound Spike, plus all the murders...

... is Angelus a Vriska?