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#cripple shit
justsomerandomgay · 3 days
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i remember being ten years old and wishing to die rather than experience the pain i was in yet still my parents and my doctors didn’t believe me. sometimes it just hits me. that wasn’t a normal experience for a ten year old, was it?
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defiantcripple · 2 days
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I just got forearm crutches to use until I get smart crutches, and my wrist hurts from using them. Does anyone have advice on using them? (I am also gonna look up YouTube videos, so please don't suggest that)
I'm scared I've fucked my wrists up :(
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I love young cripples with stereotypically “old people” disorders! (Personally I have severe plantar fasciitis at 20)
You’re not “too young” to have this pain.
You don’t need to “wait until you’re older and then you’ll see”.
Your disability is a disability regardless of your age!!!!
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azztiph · 6 months
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Self destructive behavior pertaining to disability isn’t talking about enough
Forcing yourself to do activities that you know will hurt your body is bad!
Making yourself not use your mobility aid when you know you need it is bad!
Not taking your medicine because you want to get worse or just don’t care anymore is bad!!!!!
I think that mental illness can definitely manifest differently for disabled people. It’s not rlly talked about because this all stuff that ableds see as inspiring or us pushing through. It is just harmful behavior.
Since every single disabled person is or has been mentally ill this stuff is just seen as normal.
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chronicallycouchbound · 8 months
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Ugly Laws. Creepy coming from the word cripple. Freak shows. Fear of clowns. Bearded ladies with PCOS & intersex variations. Contortionists with EDS. Little people. “Missing links” people with Microcephaly. “Snake man” people with limb differences. Lack of welfare programs. Disability rights. All of these things are connected.
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tinyleafkid · 7 months
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i don’t have many tumblr followers, but i’m desperate to get this as far out into the world as i can
i’m in desperate need of a wheelchair, and i don’t have the money to make that happen
please help and share if you’re able
https://gofund.me/81a4e7a4
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minimallycreative · 15 days
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i love how sometimes, despite all the medical advancements of the 21st century, the only thing that relieves pain is sitting/laying/standing in a weird position because it places/doesn't place pressure on certain spots
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witch-wagon · 1 year
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Reminder that if a disabled person says that they’re disabled they’re fucking disabled. They’re not “differently abled”, it’s not “but you’re capable of doing other things”, they’re fucking disabled. Don’t come up with excuses for them, don’t try to make it seem like disabled is a bad word, just shut up and listen.
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cistematicchaos · 2 months
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The psych ward was hell for so many different reasons (most of the staff hated Mad people, the food was mostly inedible, it was a glorified prison, ect) but one of the worst parts for me was how inaccessible it was as a physically disabled person.
I wasn't allowed to have my cane or my earplugs (both of which I need), I was "required" to shower daily or get marked as "noncompliant" even though I have severe pain issues that make that near impossible, walking was a constant requirement because not only were there "meetings" and "classes" that you attended or got marked "noncompliant" but if you needed water or I dunno help you had to walk to the front desk and ask. You also had to walk to the nurse's desk and stand in line to get medicine or get marked as "noncompliant" because she sure as hell wasn't going to bring it to you.
I was constantly getting both my glasses and my sunglasses taken from me by people who did not believe I needed them and the chairs were all hard plastic that did not work well with a broken body.
They also did not keep food allergies in mind and lactose intolerance also did not count as an allergy so that was hell too.
I have chronic migraines but "wasn't allowed" to take any medicine for it unless I wanted one ibuprofen. There were also windows everywhere and no curtains which went beautifully with super bright lights, so I never ever felt like I wasn't dying from a migraine and general light sensitivity. There were no quiet rooms, no dark rooms, nothing but light and loud. I was also taken off all my pain meds for over a day because they "weren't sure" if I "actually needed them" and I was taken off my heart medicine repeatedly because they really just thought I was too young for that.
I was given a walker instead of my cane, which does not work the same, and doctors constantly kept trying to take it away because "you don't really need that, do you?". There was often not enough space in certain areas for my walker which made me extra vulnerable because when I was being harassed by people, I couldn't just walk away and staff was pretty much useless.
Not to mention, we were "encouraged" to wake up at five in the morning every day and if we didn't, it would get written down, which is wild because my pain meds require I get a certain amount of sleep or they fuck me up.
It would've been hell even if I wasn't physically disabled but I am and all I could think the whole time was about people who had worse physical disabilities than me and needed more support and accessibility and how they would get or did get treated in places like this. There was almost no consideration all the time and staff was actively hostile over it.
A bunch of psych wards refused me as a patient because my files show I'm physically disabled. What are we supposed to do? Where the fuck do they think we can go?
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acarwrotethisrice · 8 days
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Body horror
I am a cyborg because I’m disabled; metal and gears keep me up and moving
I am a vampire because I’m chronically ill; hungry for the life force coursing through people
I am a mummy because I’m disabled; all bandages holding together a failing body
I am a zombie because I’m disabled; all crawling dragging movements
I am disabled because I’m a human. I am a human because I’m disabled
my body is not horrifying so I am not body horror
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blue-genes · 10 months
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I will stop "exploiting" my disability to get free stuff when healthcare is affordable.
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justsomerandomgay · 14 days
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getting disabled over a period of time is so weird, because sometimes i’ll just see something, let’s say about running, and think “i should do that!” and then i slowly realise that i can’t run anymore. i can barely even walk. it’s weird because there wasn’t one event that happened that made me like it. there wasn’t a day where i woke up and couldn’t run anymore. it was slow and gradual. and sometimes i realise how much ive lost that i didn’t even realise because it all happened so gradually. sometimes it feels like yesterday i could run and today i can’t, and sometimes it feels like forever ago that i could.
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defiantcripple · 22 days
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I am becoming convinced that able-bodied people do not actually know what experiencing pain is like based on the way they talk about it.
To me, developing chronic pain gave me this moment where I was like, "Oh, this is what being in pain is ACTUALLY like. I am 24, and I have to learn how to be in pain." Sure, I've had twisted ankles, I broke my arm, I've had the flu. Temporary pain hurts and is valid, but you don't learn how to actually be in pain until you are in it all the time. It's a hard lesson to learn.
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yrfemmehusband · 9 months
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hi chronically ill and disabled ppl how do you deal with the feeling that your illness or disability taints every positive experience in your life asking for a friend (i am struggling)
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azztiph · 9 months
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Needing a mobility aid but being unable to get one because of ur parents is actually so frustrating!
Sorry to all the people who r too young to get one on their own
Who can get one, but face too much pressure from their families not to
Who r told that getting a mobility aid is basically giving up
And last but not least!
One big FUCK YOU to ur ableist family
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I’m Native American. If a start a movement for specifically my tribe (Ayamara & Quichua) to discuss issues specific to natives in the Altaplana, other natives aren’t going to start complaining that they’re being unfairly excluded. Me starting a group for people like me isn’t saying that other natives aren’t native, and it’s not invalidating their indigeneity.
Following so far? Great.
So then why is it that when a marginalized group like physically disabled people want a movement specifically about the struggles we face as physically disabled people, we’re told we’re unfairly excluding others?
Why do people feel entitled the cripplepunk movement, a movement and space that isn’t for them, especially when there are plenty of movements that center their experiences?
There are two main reasons I’ve seen:
“””””internalized”””””” ableism: you feel as if your mental disability doesn’t count as a disability, so when you’re told that you can’t participate in a space for only physically disabled people, you feel as if that confirms your ableist internal belief that you’re not disabled enough. “Internalized” is in quotes because people with this attitude really just externalize it to hurt others.
“””””Lateral””””” ableism: as a disabled person, you hold and perpetuate beliefs that echo the wider structures of institutional and systemic ableism, and you feel entitled to hold those beliefs because you are disabled. This is comparable to trans people who are transmedicalists. “Lateral” is in quotes because most of the time, people who hold this attitude are lashing out at people with a completely different disability than them.
So let me ask you: why do you feel so fucking entitled to a movement that’s NOT FOR YOU?
And before you say “I’m physically disabled and I think it’s fine for non-physically disabled but mentally disabled people to be included”, re-read the “lateral” ableism point. Your ableist opinions aren’t correct just because you’re disabled.
DISCLAIMER: I’m not saying mentally disabled people aren’t disabled or that one kind of disability is always worse than the other. Any BS in replies will either be mocked or blocked.
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