Hi guys! Here’s some advice from a cane user on how to spot a fake cane user/disability faker!
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.
ah fuck (said politely but also horrified)
Discord has been implementing a feature where direct links to images uploaded to Discord will no longer work after 24 hours. If you want more information, please check out this post by twilight-sparkle-irl. As Pluralkit and Tubberbox both use the direct links for images uploaded to discord for member avatars, this will likely affect these two bots.
I've talked to the Pluralkit devs and they have informed me that Pluralkit and Tubberbox devs are in talks with Discord to see how this will affect the bots. No updates as of yet but once I hear anything I'll update this post.
In the meanwhile, I highly suggest everyone to save alter avatars if they can. I'll be providing a link to an external tool that you can use in the reblogs of this post.
UPDATE: One of the helpers/mods for Pluralkit/Tupperbox has made a post about the situation. I definitely recommend people to read it when they can. If Tumblr breaks the link, I have a reblogged version of this post with the link there.
Social isolation can be traumatic.
Neglect can be traumatic.
Not having friends can be traumatic.
Being alone all the time can be traumatic.
Bullying can be traumatic.
Don’t let anyone else tell you otherwise.
Your struggles are valid and you deserve to be seen.
-Dr Sunshine
reblog if the best idea that you could come up with was falling over and lying on the ground like a lump
If your first reaction to a mental disorder is to demonize it, you're ableist.
Yes, if your first reaction to paraphilias is to demonize them, you are ableist.
Yes, if your reaction to NPD/HPD/ASPD is to demonize them, you are ableist.
Yes, if your first reaction to actual intrusive thoughts is to demonize them, you are ableist.
DID is simultaneously the most subtle, ambiguous disorder while also being the most intense, all-encompassing, extremely-personal-because-it-affects-fundamental-perceptions-like-memory-and-identity-at-all-hours-of-the-day disorder of all time.
sometimes i start to slide back into the mindset of "what if I'm not really disabled and I'm just faking it" or "what if everything could be cured by just doing x, y, z" etc.
and then i remember that during lockdown in 2020 i spent 6 months — like every single minute of that six months — focused on taking care of my health and doing everything right
i slept 8+ hours, i drank lots of water, i got a decent amount of (non-straining) exercise, i went for walks and got fresh air, i ate balanced meals, etc. etc.
and my health got worse.
i did everything right, continuously, for months, and was still disabled. there is literally nothing i could have done to "fix it". i'm not faking it, i was alone (mostly) and trying to convince myself that everything was fine, and i was still in debilitating pain.
everything has been so much better with disability aids. having my cane has been life-changing. using sensory aids, life-changing! a non-disabled person wouldn't benefit this much from disability aids!!!
i think this is coming up again for me because I've become a relatively well-known person on campus for disability (and queer!) issues, and despite having all of my lived experience and the drive to deal with things, i still feel underqualified.
there are other people who are "more disabled", or have "been disabled" longer than me (since things were really only dealt with during lockdown after my experiment, it's only been like 3-4 years with a diagnosis). sometimes i feel like i'm taking away an opportunity from someone that would be more qualified to do things.
logically though, i'm not. most of these things i have either started myself, or other people have convinced me to get involved with because i seem "qualified" to talk about it. I've had four meetings this week about campus accessibility, people actively seek me out to ask questions, i do regularly deal with ableism and inaccessibility even if it's to a lesser extent than some other people — but the stuff i'm doing is to help everyone, not for personal gain. i'm not pretending to be disabled for selfish reasons. there are clear access barriers that directly affect me as well and i am doing everything in my power to take them down.
anyways you can't really fake being disabled, especially not to yourself. ;)
Here’s my metaphor for systemhood that I tell my singlet friends.
Imagine you’re playing a first person video game. You have the controller, you control your character. It’s a normal first person game. You are an alter, the character is the body. This is fronting.
Other people live with you. Sometimes, they come into the room and sit and watch while you play. They sometimes try to guide you, give you advice on what to do next. They don’t always agree, and they can argue with each other. Other times they scream at you that you’re doing everything wrong and you suck at this game. This is co-consciousness.
Imagine how distracting it would be for people around you to tell you what to do, or to scream at each other or at you, even if they have good intentions. It wouldn’t be easy to focus on your game, would it?
Then sometimes, something happens in the game that prompts you to hand off the controller to someone else so they can play and you get a break. This is (some types of) switching. This can be good.
Other times, someone rips the controller out of your hand or fights you for it. This is (other types of) switching. And sometimes, six other players hook up their controllers, but there’s only one character to play as. So all of you have your controllers, but you’re all trying to play the same character. This is cofronting.
Imagine how difficult that would be. Imagine how hard it would be to try and play a game while someone is trying to take the controller from you, or while six other people are trying to play too.
There are also times that nobody is playing, or you can’t decide who should play. What’s happening to the character in the game? What are they doing if no one is playing? This is dissociation. The character is doing nothing. They’re stuck.
This is the best metaphor I have come up with for being a system. It’s something a lot of people get because they’ve played games before.
I wonder how soft these feathers feel.
really, just an excuse to draw some pretty wings...
"ohh what if my kid starts identifying as a CAT because of the trans agenda we have to prote—" well they've always done that. do you remember the psychological effects of h2o on young girls. of warrior cats on autistic children. i believed i was a demigod because of percy jackson. twilight came out and kids were telling their friends they were secretly vampires. this is just a thing kids do. worry less
It is inherently fun and sexy to say statements that swap the traditional genders of pronouns and terms mid-statement, such as: "I'm going to make him my wife" "She's my boyfriend" "Who says a guy can't be a pretty princess?" "That girl's the coolest dude I've ever met" "She's a madman who has to be stopped" "It's not his fault he's a material girl" Gender is a set of watercolors and the prettiest shades come from mixing the paints together.
Zero : They/Thema big ol' fruit with lots of love to give⭐️icon by @time-woods
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