#this post is about physically disabled people

[cripplecharacters]

Hi, I have some questions regarding confusion over a certain topic. First off, I have a character with a severe scarring on the upper right side of their body. I've heard in some tumblr ppsts that such appearance shouldn't be fetished. Then I stumbled across some posts, mentioning how the character can be described as 'pretty with it'.

For sure, I'm trying my best to normalize the looks. Because I have a love interest set up for them and while they don't mind the looks, I feel confused on how to convey their appreciation for the character's looks even with the scarring. They like the character as they are and stuff.

Sorry if this is a lot, I tend to get confused on how to handle such scenarios. And this sort of varying opinions is making me go '???'.

It's okay if you take your time to answer! Have a good day ahead of ya!

Hi!

"Fetishization of a disability" and "thinking that a disabled person is pretty" are two very different things. Despite the somewhat similar sound, they're not connected by much.

In the context of scars, fetishization would be what I would call the "Zuko situation" (yes, I love ATLA as much as the next guy, let me explain) - the scar isn't really a scar, it's more of a, I don't know, make-up? It's just the color that changes, it's all sharp edges and intricate shapes, the facial structure stays the exact same. There's no physical symptoms. Essentially, it's permanent body paint.

It fetishizes a disability by making it inaccurate, sometimes almost mystical. You don't see anyone fetishizing how real people with facial burns look like because they only like the idea of it. They don't care for us; they don't care for Face Equality or why we are offended by "villain with scar #32482". It's just a fun splotch of color to add to your OC when you're out of ideas.

Another aspect of fetishization is the "a scar is the worst thing in the whole world", the tragedy porn. It's using a disability for cheap drama. Again; it's inaccurate and exploitative. I don't see writers excited to depict my "coming to terms with my facial difference as a teenager, and eventually being proud of it" experience because where's the shock value and pity points? Fetishization, again, is about liking the idea of it, not the real thing.

Describing your character as beautiful, well, isn't any of that.

The point that I tried to make on that post was that a scar is often considered inherently ugly. That it's a stain on someone's beauty, that it would be better if it wasn't there.

"Brown beautiful eyes, thick facial hair, strong cheekbones - he managed to be irresistibly handsome even with that nasty scar going across his nose."

This, well, sucks. It's as if the character's beauty and their disability are contradictory forces that have to fight each other. But in reality, scars and any other visible disabilities are neutral. If the character is pretty, their scar is pretty too. It's a part of them, so how could it not be?

"She was a cute girl; her pastel pink, thinly braided hair framed her face, defying gravity by curling towards her mouth. The burned skin on her lips shifted as she smiled, revealing a tooth gap. She played with her equally pink 'white' cane, holding it between the two fingers she had on her right hand, bopping it against the ground to the rhythm of the song."

This, on the other hand, just states her disability as a part of her person. It's nothing weird or shocking, she's pretty, has a burn on her face, she's blind, she's missing some fingers, she's enjoying the music - it's almost boring when compared to the usual "scar introduction". There's no "even with her horribly burnt face", no "if only she wasn't scarred she would be beautiful", no "poor thing, lost her fingers in a horrific fire" - instead, she is beautiful, and she has scars, and she sure is having fun. That's it.

This is my best shot at explaining the difference between "fetishization" and "yeah they're pretty :-)" ft. my questionable writing - I hope this makes sense.

I definitely took my time to answer, sorry about that. Thank you for your ask!

mod Sasza

[griancraft]

Hi guys, this is the donation page I was talking about to help me get out of my abusive situation. More context below the “read more”

It’s entirely optional to donate. I get being broke or wanting to support people who are in more immediate need. I hope I can pay it forward when I’m in a better place.

Most of you probably know my situation already but my parents are abusive and they have respected positions of power where I live. Both work at the university I go to and one of them is close with my boss at work. if I were to speak out about anything I went through I would not be believed because of how “nice” and “respectable” my parents are. I would lose housing and potentially way, way more than that. To mutuals I can show a bit of proof in dms but I am afraid of even posting what I have in case they find it.

I wasn’t given many shifts in May and I am unable to work in June at all. My aim is to leave the country by mid September. The plan is to go on a working holiday visa to go to live with my partner in their country, and I know that sounds extreme but I do not want to be anywhere where they can easily get to me. It’s also a place I know I will have housing.

I do not expect anyone to pay for this but me, and I am working 35 hours a week right now and will probably be working full time in the summer. But I’m also physically and mentally disabled, and my ability to work is sorta limited sometimes, so help would be really, really nice. I’m really sorry for how wish washy I’ve been these last few months it’s getting really bad.

[leidensygdom]

Ok, I'm gonna start a post idea I had been pondering. If you're either mentally or physically disabled and you have opinions about representation, this is the thread for you!

So, I've been seeing more people trying to tackle the topic of autism in their stories, but I've felt some of it tries to woobify a bit what is to live with autism, or just focus on the more socially acceptable quirks of it. And as someone with autism/ADHD (was suspected of it for most of my life, got it finally diagnosed by my therapist (who specializes in autism and ADHD) last year), sometimes I'd like for people to acknowledge the more unsavoury parts of it, the weird quirks, etc.

So, this post is going to be about that- If you wanna help people understand how your disability/neurodivergency affects your life, feel free to add to it! Just mention what do you have (no need for a full list, just what you consider relevant to the post) and some experiences, quirks, anecdotes or such that you think that are not often seen in stories or media, and that you consider an important part of it. They don't need to be huge things! I encourage people to share just whatever they feel comfortable. My list is gonna be a mix of stuff, but yours can be very different. Let me start!

Clothes and how they feel was surprisingly one of the most disruptive parts of my autism. As a kid, if I was forced to wear something that caused me some bad texture/sensitivity issues, it would significantly affect my behaviour and performance. It took me many years to be allowed to use mostly sportswear. (And it turns out being a "girl" (not anymore) wearing only sportswear tends to cause a whole lot of bullying)

This happens even nowadays. I've found out that non-heeled boots are more comfortable to me than sport shoes, because feeling something against the back of my foot makes me feel overwhelmed. I tend to wear yoga pants under actual pants, because they keep the actual pants' seams from causing sensory issues. There's almost a sort of ritual on how do I need to combine clothes to be able to function "normally", mostly consisting on reducing how much they annoy me.

On that topic, hygiene is actually a huge thing too. As a kid, I wasn't allowed to shower daily. Days I didn't shower, no matter how much I tried to keep my hygiene in other days, were "bad days" to me. I would literally plan hanging out with friends or eating out around the days I was allowed to shower. I could physically feel the difference between the day I showered and the day I didn't (even if I washed my face, armpits, used the bidet, etc).

This is true even nowadays. I can thankfully now shower daily, which isn't recommended by a lot of experts (specially because it can damage your hair and skin), but it's more worth to me than having days where I feel like I shouldn't be seen in public.

Being overwhelmed sucks! Meltdowns are mostly associated with kids, mostly because adults either learn to mask them, or do everything they can to AVOID having that meltdown. I've mostly figured out routines and such. There's this one place we go eat out every other Tuesday- And in the hours we go in, there's a sort of silent corner that is always free. This week's schedule was a mess, so we went yesterday to that same place, and the silent corner was filled with a very loud group. I got extremely overwhelmed. But enough masking drilled to me means I just sat there unable to talk for maybe 30 minutes.

Autistic adults still do have autism and experience often the full spread of traits, they've just found ways to mask, or avoid being in situations where they do need to do that. I've adapted my life and routine to that. But sometimes I land on situations out of my comfort zone that will make me feel just like when I was a kid. I want to freelance online because I'm fully aware I can't perform properly in a public facing job.

Group projects sucked so much. I know they suck for most people, but most times it was easier for me to do the entirety of the project by myself and add the others' names to it than dealing with chasing people for their parts. My college had a 6-months-long massive group project in the last year, with a 7 people group, which obviously I couldn't do alone. The whole experience was so harmful in so many ways I've had several full therapy sessions talking about it :'')

One of the reasons it's because mental flexibility is HARD with autism. If i set a schedule, I expect that schedule to be followed. If people agree to do a part, I expect that part to be delivered (unless there's a proper reason) on due time. People hate this a lot usually! It will tear group projects apart!

Stimming can be harmless, or it can be very annoying to some. I tend to shake legs and play with something in my hands. I could easy this off drawing in classes- My high school found out that I was paying more attention when I was allowed to draw in classes, and my academic performance was pretty much perfect, so they gave me permission to do that.

However, I had a teacher in middle school that did forbid me from drawing. I stimmed during a class with pens- She got so mad she sent me home with a note to my parents they had to sign. Fun!

Not exactly an anecdote, but I am ace. I hate the discourse about "making an autistic person be aro or ace is infantilizing autism". Aro/ace people can have autism. That's just how it is. I've been infantilized a lot for being ace- Which only got worse because I am autistic, and people perceived some of my special interests as child-ish. The combo didn't make things easy.

On that topic, people will often be very patronizing of your opinions or takes for being autistic. I've had people debate my sexuality (or lack of thereof), my gender identity and presentation, my hobbies, my preferences for everything, down to "what do you want to eat tonight?". This isn't too different to shitty takes about how "autistic people are more prone to being affected by the trans activistsTM", because people assume autistic people can't choose on their own. Trust me: We can.

Anyhow, I'd love if this post could be a good compilation of these sort of anecdotes! I think it could help people who wanna learn more about what is it to live with specific disabilities (and how to better portray them in media)

[official-locke-writing]

Hey guys, I know I've been serious-posting quite a bit more than usual lately, I just wanted to talk a bit more about how (and why) I write my characters the way I do in terms of realistic portrayal and my take on mental health issues in fiction, mainly Creepypasta and Slenderverse.

It seems like some people take me for an able-bodied, mentally stable human being "looking in" on mental health who assumes that I know everything because I Googled some stuff. I can see where this view can arise, as I have never truly spoken about my disabilities or personal life much at all. It occurred to me that you don't know much about me, or why I am so passionate about things like this.

So, let me be transparent.

Yes, I have studied abnormal psychology as a focus in college, but that is not the source of my interest in exploring mental health in the fashion that I do. I have a literal shopping list of physical and mental health obstacles that I deal with daily, and being able to understand it better and connect with characters who share a more accurate depiction of the struggle feels more personal to me than a more standard "fanon" depiction of Creepypasta characters. It's how I like to write things.

I have Marfanoid Habitus Syndrome, Ehlers Danlos Syndrome, childhood-onset Rheumatoid Arthritis that is in later stages now that I'm an adult, along with heart conditions like Postural Orthostatic Tachycardia Syndrome (POTS), heart valve abnormalities, and Chronic Fatigue Syndrome. I deal with Borderline Personality Disorder and autism which can cause episodic confusion, emotional distress and panic attacks. I am not asking for sympathy by saying this. I just have these things, and it's a part of my life.

Needless to say, I know what it's like. I really do, which is why I have such passionate interest in rewriting Creepypasta characters to be the way that they are. I just thought you guys would like to know that my differing views on how I would like the characters to be should not, in any way, feel like an affront to your depictions. I may not agree with them, but whatever, y'know? It's the internet. Differing depictions should not equate to waging war about who is right.

I will address this specifically to the people who want to "call me out" on being ableist because I changed some mental health depictions regarding my Toby rewrite to be less noticeable: Mental health issues are not always the forefront of someone's personality nor behavior. I can promise you that people think I'm normal on first look because all of my medical conditions are "invisible." It comes with the package, and I think anyone with an invisible disability can agree with me that the original stories in the fandom are... incredibly strange and even a little offensive. I'm not a fan.

And I will state, I know this character is outdated and I am not bashing the creator, and I am well aware of their need to be detached from this character due to the poor writing, but Ticci Toby does truly belong to the fandom now, and the fandom has held up these pretty wild design choices. I'm looking to change that in my personal depictions and hopefully foster a healthier way of using these characters to cope.

I love you guys; I hope I'm making sense here and am trying to touch base with you all in hopes of clearing up some misunderstandings. I'm not participating in the erasure of disabilities; I'm participating in realistic writing.

[azztiph]

Sometimes u just need to sob and scream and cry and bitch about ur disability

I think a lot of people feel like they need to be at completely at peace with their disability

And you don’t!

Be mad be sad be pissed off!

[butchfalin]

the funniest meltdown ive ever had was in college when i got so overstimulated that i could Not speak, including over text. one of my friends was trying to talk me through it but i was solely using emojis because they were easier than trying to come up with words so he started using primarily emojis as well just to make things feel balanced. this was not the Most effective strategy... until. he tried to ask me "you okay?" but the way he chose to do that was by sending "👉🏼👌🏼❓" and i was so shocked by suddenly being asked if i was dtf that i was like WHAT???? WHAT DID YOU JUST SAY TO ME?????????? and thus was verbal again

[varian-ross-horror-author]

"Disabled people should be allowed to be as independent as we can be" and "disabled people should not be pressured to be hyper-independent in order to not wind up in nursing homes against our will" are two thoughts that can, and should, exist at the same time.

[rjalker]

Dear people who aren't physically disabled who plan to write fantasy settings:

[ID: Several images taken from the Geordi La Forge yes and no meme format, with Geordi holding out a hand disapprovingly for the no section, then pointing in approval for the yes section.

The first image is the meme:

No: "Saying the existance of magic in your setting means there are no disabled people (this literally just means disabled people are killed. AKA eugenics)"

Yes: "Having disabled people who use magical mobility aids and other assistive devices. Realizing that someone is still disabled even if their prosthetic arm is made of magic instead of plastic."

This is followed by four more panels of yes section:

"Geordi la Forge is still literally disabled. His visor helping him does not erase his disability and make him magically abled."

"Toph from Avatar: The Last Airbender is still literally disabled even though her Earthbending helps her. It does not make her disability ~magically~ go away."

"Having your disability be accomodated does not mean the disability goes away. Having a prosthetic hand, even one that's made of magic, does not mean you're not disabled."

"Magical mobility aids do not mean disabled people don't exist. It just means they use magical mobility aids instead of plastic or metal ones. A limb made of magic is still a prosthetic even if it's made of the soul of the universe instead of plastic and metal."

Then another no panel: "'There's no disabled people beacuse magic'".

Then one last yes panel: "'Magic helps disabled people in a variety of ways'".

End ID.]

This also applies to science fiction; just because Luke Skywalker's prosthetic hand is super advanced doesn't mean it's no longer a prosthetic, or that he's not disabled. Same with Darth Vader - just because he has a suit that lets him breathe and walk around doesn't mean he's not disabled. (And Star Wars' propensity for making the villains visibly disabled while the heroes disabilities get covered up by super advanced prosthetics is a topic that deserves its own post, especially with how ableist some of the authors of the books are. Troy Denning is especially ableist)

Edit:

Because people keep being fucking obnoxious and ableist in the tags, yes,,, motherfuckers, if you refuse to have disabled people in your setting, that does make you fucking ableist. If you say that the magic is used to cure all disabled people and that's why they don't exist, that's fucking eugenics.

You cannot ""cure"", more like remove all disabilities without fucking eugenics. Magically automatically destroying disabled fetuses (a very fucking popular trope!) is eugenics.

The only way to fucking "cure" autism is to fucking kill all autistic people, also known as eugenics!

What about people with PTSD? Do you just fucking brainwash them so they aren't traumatized anymore?

Do you force all Deaf people to be able to hear? Do you force all blind people to be able to see? Do you force all anosmics to be able to smell?

Do you magically force everyone with a speech impediment to speak to your standards?

Do you force everyone born with bodily or facial differences to live up to your fucking standard of beauty?

You cannot fucking say "disablities don't exist in this universe because magic cures everything" without inherently saying that eugenics exists in your fucking universe.

Not all fucking disabilities need a cure. If you ""cured"" my autism I'd just be fucking dead. You'd literally just be changing me into what you think is fucking acceptable.

Stop fucking arguing in defence of ableists on my fucking post so you can pretend that eugenics has never been written about in magical settings when it is extremely fucking prevalent.

And while we're fucking at it, let your gods damned characters become disabled over the course of their story, and call them disabled within the fucking story. I don't care if they're a robot. I don't care if they have magic. Not all fucking damage can be fixed. Curses exist. Hardware can go out of fucking date and no longer be manufactured anywhere.

Let your characters become disabled and do not magically fucking cure them back to brand new every single time they get hurt. The only thing you accomplish by doing that is destroying any chance of ever having stakes.

No, "magical healing leaves scars on the mind from the memory of the injuries though!!!!" is not fucking good enough. Let your characters have scars. Let them become disabled. Stop being fucking ableist cowards.

Edit number fucking 2:

No, motherfuckers, you do not get to comment "if the disability was caused by magic it's not ableist to cure it with magic". You are the ableist this post is about. Shut the absolute fuck up, stop treating being disabled as the worst possible outcome, and just admit you're a fucking ableist. If you don't want your characters to become disabled, then don't fucking make them disabled.

[ID: The Garfield "you are not immune to propaganda" meme, now edited to read:

"If your first thought upon reading this post is, 'Oh, but it's okay to magically cure disabilities caused by magic!' Congrats…you are the exact sort of ableist jackass this post is about."

End ID.]

Edit number fucking 3:

Autistic people exist! People who are born with disabilities exist! You cannot create a setting where disabled people do not exist because we're all "cured" or "fixed" and not inherently say that you are killing disabled people as soon as they're born, or fucking aborting us as soon as you figure out we'd be born disabled! That's fucking eugenics!

There is no way to "cure" autism without eugenics! There is no way to "cure" people with body differences without eugenics! There is no way to make disabled people nonexistant in your setting without eugenics! Thinking you can and should "cure" and "fix" all disabilities IS EUGENICS!

Also:

[ID: A character shouting at the camera, now edited to read: "Shut up about Dungeons and Dragons! Shut up about Dungeons and Dragons! If the rules of Dungeons and Dragons are ableist, then fucking change them! It is your fucking personal responsability to be a better person than your bigoted society wants you to be!". End ID.]

[ID: White text on a dark brown background with white and black borders around the edges, that reads:

"I don't fucking know or care about Dungeons and Dragons.

This post is not about Dungeons and Dragons.

Do not fucking throw the rulebook of Dungeons and Dragons at me like it's some sort of 'Gotcha!'.

You will literally just be blocked like the rest of the ableist assholes who've already tried it.

If you play dungeons and dragons, it's your responsability to make your games not be ableist, even if it means breaking the rules.".

End ID.]

I do not fucking care what the ableist rules are in Dungeons of Dragons. Do not fucking throw ableist rules for a game I have never and will never play at me on a post I made so that people could learn how to make their settings less ableist. If the rules in Dungeons and Dragons are ableist, then fucking change them. If you don't want to change them, then stop fucking playing an ableist game.

Disabled people deserve to see ourselves represented in fiction just like everyone else, without any fucking requirements that we be "cured" or "fixed" before the story ends.

How the fuck would you feel if a trans and gay character's whole story revolved around going on a quest to become straight and cis, did so, and only then was allowed to live happily ever after?

Why do you fucking think suggesting people write stories about disabled people going on a quest to be cured because it's the only way they'll ever be happy is any less fucking offensive?

Also:

This post is NOT a place for you to talk about how disabled people in fiction should have the option of curing their disabilities. It's just not. That's the fucking default for this society. That is not a revolutionary concept. It's not novel. We fucking know this society wants us gone. A post about how disabled people deserve representation is not the place to talk about how "Well, actually, in fiction disabled people should be cured!" Like that's not the fucking universal default???????????

Edit #4:

Everyone needs to stop tagging this singing praise for Fullmetal Alchemist. A story that uses disability as a punishment and the characters are on a quest to cure their disabilities is not the amazing representation you're all claiming it is just because the character who is only disabled because of DIVINE PUNISHMENT uses prosthetics.

Read this post, and this one. Fullmetal Alchemist is a hell of a lot more ableist than you people are letting on.

guess what you can now find a PDF version of this post on the web archive.

Edit #5! August 23rd, 2023!

A) Everyone. Disabilities that can only exist in the magical setting are still disabilities.

Trying to cure the younger brother's magical disability of being a soul floating around in a magical suit of armour is, in fact, going on a quest to heal a disability!

It doesn't matter if the older brother doesn't want to get his limbs back when they're going on a quest to heal the younger brother's disability! Especially when they BOTH get magically healed at the end!

Magical disabilities that can only exist in that setting, but not real life, are still disabilities, and it's not okay to magically heal them either! What part of the Garfield meme on this post did you all choose to ignore?!

B) When you leave tags on a post you are reblogging, the original poster can see them! When you leave tags on this post, I can see them!

If you think this post is ""too aggressive"" then simply do not reblog it! Don't fucking tone police me on a post I've had to edit five times now due to the constant ableism people have been commenting since I made it!

I have been called the R slur by multiple people in response to this post! People have literally reblogged this post to defend eugenics abortions! You can't see these comments or replies anymore because I blocked the poster!

If you think minorities are being too aggressive by responding appropriately to bigotry, you're a bigot! And you should either not reblog the post at all, or at the very least, shut the fuck up and not tone police us!

Do not fucking put tags on this post complaining I'm being too aggressive! That's called tone policing and you're a bigot if you do it! Don't fucking do it on anyone else's posts either! They can see your tags too!

C) When I fucking say Harry Potter fans are banned from this post, yes, this means YOU!

Either stop supporting a billionaire who's literally using the profits from her bigoted shittily written books to fund REAL FUCKING GENOCIDE, or fuck off!

By continuing to support the Harry Potter series, you are literally giving JK Rowling free fucking advertising! You are encouraging more people to read the series and watch the movies, spending more money and giving her more fucking money with which to LITERALLY SHAPE A COUNTRY'S LAWS TO COMMIT GENOCIDE. She is literally fucking fighting to make being trans illegal! She is literally fucking fighting to have even more of autistic people's rights taken away!

You cannot fucking be a fan of the Harry Potter series in 2023 and call yourself an ally to all the minorities harmed by JK Rowling and the bigotry baked into her shitty series!

Read another book! The Web Archive has tons you can read for free! Literally every single book on gutenberg.org/ is free! Including audiobooks for some of them!

If you write Harry Potter fanfiction, simply fucking get rid of the names and identifiable features and start writing original fiction instead! It's literally free!

Not supporting a literal fucking genocidal billionaire costs LITERALLY NOTHING! And if you refuse to fucking stop supporting JK Rowling, which is what you are doing when you support the Harry Potter series and squeal over her OCs, you are not an ally to any fucking minority! No! Not even if you're trans yourself!

= = =

Edit again Nobember 28th 2023 because this comment is just. such a perfect example for all of you that think this doesn't happen.

butter-whore2 said, two hours before this edit:

kind of a fan of tumblr's slightly more algorithmically elements for reminding me of the hell's other people construct for themselves but this one hits like five of the boxes. How do people do this to themselves? it's such a bizarre way to act over media I genuinely do not believe is capable of stirring an emotional response the metaphysics of disability here are unintentionally really funny but disability is not a coherent ontological framework, it's a vague descriptor for literally thousands of different things none of which lend themselves to categorizing Moralizing over fiction is incredibly lame.

Liking harry potter is also incredibly lame, it's not morally wrong nor transphobic and you do not get to decide that lol. people literally do get "cured" of their disabilities all the time, many of them have a positive experience in doing so. this is not what eugenics is.

the anti abortion stuff lol

Literally how do you live like this? you guys don't even read real books I don't get it.

Archived version of the comment for posterity.

So yeah, lofl, block this fucker.

[consider-your-potatoes-mashed]

Why the fuck is it so hard for able bodied people to get their heads around the fact that specifically physically disabled people are not actually accommodated most of the time?

Whether it be the inaccessibility of a building due to stairs, heavy non auto doors, ramps that are too steep, broken elevators or just non existent elevators, etc the list goes on and on. Or now public spaces that let’s say are otherwise perfectly accessible are now inaccessible to so many people because so many people refuse to wear a fucking mask when it would cause then no harm (maybe just a bit of sweat) to wear one.

The fact that abled people don’t see just how fucked up and inaccessible the world is blows my fucking mind. Just because someone “can” do something or go somewhere doesn’t mean they should have to do that or that it’s safe for them to do so. Like sure I can do stairs but holy shit by the time I’m at the top I’m in so much pain and I feel like I’m gonna pass the fuck out man.

Bottom line, the world is really fucking inaccessible and that needs to be fixed. Physically disabled people’s voices need to be listened to and not talked over by ableds who think they know what’s best for us or who think the world is perfect as it is

[varyathevillain]

no joke but what I really want for Buddy Daddies as a fandom is to make fanart and fanfic post present time ep12 where Rei wears an arm orthosis when working.

I think varied disability aids being represented would be fantastic, and personally would write Rei as someone being deeply proud of something he's done for his family, but also understanding with time that using an orthosis also helps him at work and in raising Miri. with a giant portion of mobility/motorics aids being represented by prosthetics, seeing more variety and exploring it in fiction would also help making a step in normalising disability treatments.

[thecorvidforest]

i fucking hate how for so much of the year people will claim to be disability allies and then september hits and suddenly they’re super excited about the horror movies and games and costumes that profit off of the fear of the the visibly disabled and those with “scary” mental illnesses. you can’t simultaneously be a disability ally and also spend your spooky season ignoring the blatant ableism in horror so you can delighted at how scary we are to you.

[cautiousgoose]

When abled people try to make your disability out to be more of an inconvenience to them than it is to you.

Like oh, me sleeping all day because I'm exhausted and in pain is hard for you to see? No worries, it's totally good for my mental health to not be able to do shit like everyone else! Good to know I'm a burden to you on top of being unable to do the things that I want and need!

Anyway, I think disabled people should get compensation every time ableds make our disabilities about them.

[transmasccofee]

thinking yet again about Saiki‘s’s final choice in the series being “I’d rather live with my powers than die without them” bc that is seriously the single best ending of a disability narrative I’ve seen. Fuck.

[iliveinprocrasti-nationn]

people have GOT to be more comfortable with some spaces not being about them. sometimes spaces are not for you. sometimes you will be told you cannot enter a space because it’s not for you. or you cannot bring a friend because a space is for you and not for them. that’s ok

[azztiph]

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.

[thedisablednaturalist]

Tw for weight loss mention

The whole exercise will cure your disability thing is a fucking joke. Yes exercise is beneficial for your health, but only if you aren't already on shaky foundations. You need to be on a treatment plan that WORKS before going into the maintenance phase. You wouldn't do regular maintenance on a broken item, you'd work on getting it up and running first. And maybe it would even need specialized maintenance afterwards if it's especially fragile.

I have fibromyalgia and acute degenerative disc disease. My immune system attacks my nerves and discs in my spine are slowly calcifying and causing the bones to constrict and damage my nerves (i think thats how it works). I have days where it feels like my body is on fire from nerve pain and days where it feels like my spine is about to rip from my back. And days where I have both (like today!). I get numbness in my hands and feet. I have horrible migraines. I can no longer walk unaided more than maybe 5 minutes without severe pain. I have something wrong with my knees and hips but the doctors don't know what yet.

You'd think I live an obviously seditary lifestyle correct?

Hell no.

I walk aided on average 6 miles a day over difficult terrain OUTSIDE of regular activity almost everyday. My legs are muscular and strong. I get my heart rate up and a good sweat, like all the gym rats swear on. I am often doing physical labor such as weeding, digging, sample collecting, pruning trees etc.

I'm not saying this to make other disabled people feel bad or prove that they can do anything if they just tried harder. This is an extremely painful lifestyle I've chosen that takes a lot of lifestyle management AND BOUNDARIES to keep up with the work. I also have an extremely forgiving boss who is also physically disabled and knows what I'm going through (deciding between your passion and your health and having to do so each and every day) No one should ever be expected to do what I do. I'm not even sure if I should be doing this myself.

This is to prove that exercise? Has not cured me. My muscles are strong but still hurt as if they're broken and I have to take more breaks than my coworker. I am constantly getting out of breath and I flare up regularly if I'm not careful. I am in excellent physical condition outside of my disabilities. I go to different doctors several times a month to get checked out.

I previously went through a diet program and lost a lot of weight (basically starving myself and got off my depression meds which cause weight gain but are also the only ones that work) and guess what? That didn't do shit either!!! I still felt horrible!!! I've since gained back the weight anyway after switching to focusing on adding more nutrient dense foods than taking stuff away from my diet (also muscle weighs more than fat, and fat helps cushion my aching joints and spine).

The muscle doesn't do shit for my disabilities outside of maybe some stability. Exercising everyday doesn't make the pain go away. Without my medications and aids and nutrition plans and steroid injections and spinal adjustments and physical therapy (that takes my fibro and spine into account) and alternative work methods I WOULD NOT BE ABLE TO DO WHAT I DO. Exercise alone is like trying to make a car run with no oil. Yes it'll go but it'll get more and more damaged till it can't and will need its entire engine replaced!

And yet I see new doctors and they look at me and the first thing out of their mouths is do I exercise? I should try doing a little every day :) and then i fucking blow their minds when I tell them about my job. No longer can they use that fucking cop out on me. I've been through this rodeo. Ive tried their suggestions. If you are in pain and nothing is helping? Exercise ain't going to do SHIT. You need to get to a point where you can move without severe pain first (if that's even possible). Then and only then should you consider implementing regular exercise if you can. Also weight loss talk is a red flag and a cop out. They made me lose 50+ lbs before they would look into the reasons behind my pain. Weight loss did nothing for me and exacerbated my pain.

I am living proof that all that shit is a lie and a cop out. That is the point of this post. I cannot believe people with serious medical conditions are being forced to put their bodies through extreme duress just to be believed. You are not disabled because of laziness or because you sit a lot. Plenty of people live seditary lifestyles and do not live in constant excruciating pain (they may develop disabilities later in life due to this however, and should be doing preventative exercises to maintain their health)

Please, share my story with doctors. Use me as an example. I am proof that "exercise first treat later" does not work. I should not have had to wait years to have my pain validated. I'd rather hundreds of fakers get (what? A blood test? An MRI?) than one chronically ill person get told to try yoga and go away by a doctor.