DISABLED ISNT A DIRTY WORD STOP ACTING LIKE IT IS.
DONT CALL ME “DIFFERENTLY ABLED” OR OTHER BULLSHIT TERMS THE ABLEDS ARE PUSHING.
DISABLED ISNT A DIRTY WORD.
CALL ME DISABLED.
IM DISABLED.
SAY IT

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@cripplepunking
DISABLED ISNT A DIRTY WORD STOP ACTING LIKE IT IS.
DONT CALL ME “DIFFERENTLY ABLED” OR OTHER BULLSHIT TERMS THE ABLEDS ARE PUSHING.
DISABLED ISNT A DIRTY WORD.
CALL ME DISABLED.
IM DISABLED.
SAY IT

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I get so frustrated when people act like "Yesterday you used your cane on the left and today you're using it on your right!" is a gotcha and they've caught a Fake Disabled?
Not that I owe anyone an explanation, but I don't have permanent limb damage. I have a few conditions that get worse with exertion and use. Yesterday my left hip was acting up so I was supporting it with the cane and compensating with my right. Today my right hip is having a whinge about it. You'll also catch me shuffling around without any mobility aids because my arms cannot handle all the extra work that goes into lugging my ass around wherever I need to go.
Sometimes I use a cane, sometimes a rollator, and sometimes even a wheelchair if I have someone to push it for me. Sometimes all three in one day depending on which part of my body is currently fucking up the most.
It is NOT your job to police people's use of mobility aids. Nobody owes you an explanation, assume there must be one and mind your own business.
also purposefully looking for ways to expose a “fake disabled” is just something you should Maybe Not Do
What do you think of Joyofsatan.org? They claim to follow the Pagan Goddess Lilith/Lalitha, they’re pro-choice and they’re the largest Satanist group in the world.
ill be honest dude, i havent heard of them and dont currently have the time or energy to look into them. in addition, thats not what this blog is for.
what they stand for sounds great. i dont know anything but what youve just told me, so ill reserve judgement
My morning routine? That's simple: first I wake up, then I get out of bed, then I experience various ailments, maladies, afflictions, etc.
so i wore noise cancelling headphones today. specifically, on the bus ride back from school; i was too anxious to actually take them out during the school day, lmao. and one girl asked "why do you have those?" I explained a bit about sensory issues, and then just trailed off with "anyway... I need them". and like. strictly speaking. that is not 100% true. I don't need them like I need food or water. I won't die without them. And unless I'm right near a meltdown, I can usually stay in a loud room as long as I'm *supposed* to.
But I do still need my headphones.
They let me function easier and more happily. I feel so, so much calmer and safer at home... which is when I let myself wear the headphones. I felt the same way when i went to the mall in the city and wore noise cancelling headphones there.
So, like. if you have a Thing you use that you don't technically, 100% ABSOLUTELY NEED to function... keep it anyway. use it anyway.
Wear sunglasses in rooms with too-bright lights, use your cane or walker because it just makes things easier, use your wheelchair when you could probably walk, wear noise cancelling headphones or ear defenders even when you can stand to be in the room without it, use your hearing aids even if you can get by sorta OK without them, keep fidget/stim toys or comfort items around because they make you happier, etc etc etc.
You do not need to wait until you're hurting as much as you can to use the thing that helps you.

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Impending homelessness, please help
I am so, SO sorry to do this but i am desperate and terrified. As of today, 5/1/2022, me and my roommate have 15 days (5/15/2022) to find a new place to live. We were just informed of this.
We had been staying at their parent's house, but are being kicked out because the house is being put up for sale. We are both trans, disabled, and severely mentally ill, and as a result they can only work part time, and I can only do doordash as my source of income. together this nets us about 1500/month. As of right now, we are looking for help with raising enough money to cover the security deposit on a place, as well as at least the first month's rent. This would come out to around $2000.
If you are able to donate, it would be much appreciated. If not, PLEASE reblog this. We are running out of time, and every penny helps.
v*nmo: ronanbudd
c*sh*pp: pkmnbf
p*yp*l: halocore
Chronic pain when you are young sucks because there comes a point where you realise that no one else your age experiences this much pain or has to live their life around it. You realise that your older siblings could excel in school and hold up jobs fine and still have energy for things they love. You realise that your friends and peers don’t worry about how a certain activity might make them feel afterwards. You realise how few people complain about pain in everyday scenarios, where they’d otherwise have no reason to hurt. They don’t question wether tomorrow their bodies will lessen the constant pain, or try to guess where the pain will be next. No one else has the constant nagging, the way pain eats at your spirits and sucks your energy. It becomes horrifyingly clear that this is not something will pass so easily, because it has been this way for far too long. You are barely an adult, and already your plans for the future include notes such as finding a job with short hours to accommodate your lacklustre stamina. You are still in school and find that hiking through campus and between classes is a physical battle, not a simple walk. When someone asks how your day was, the defining factor for how good or bad it is entirely depends on your pain. Wether or not you agree to plans is not up to you, but your guess on how your body will cope.
That’s when it starts to hurt more than just your body.
something thats particularly pissing me off right now is how disabled people have to use every last ounce of energy we have just to advocate for our right to be comfortable. not even safe, just comfortable. do you know how exhausting it is to have to choose between using a mobility aid and going literally anywhere?
ive stopped using my wheelchair in public for the most part, because all of the wheelchair accessible door buttons are broken from people kicking them for a laugh. the wheelchair accessible stalls are taken by able bodied people not even using the bathroom when the rest of the stalls are open. the non-stairs routes to places take an extra 10 minutes if im lucky.
ive stopped walking with my cane for the most part because when im in line at the store and shuffling it between my hands so i can get my wallet, people (including the cashiers) roll their eyes at me. when im sitting down and have it propped against my chair people will knock it over and out of reach.
its easier to be in pain at this point. it is easier for me to break my body further because i dont want to spend the extra 10 minutes getting to class, wait the extra half hour for the disabled stall, get the looks i do for being disabled in public.
being disabled is inherently uncomfortable, yes, but ableds make me feel like its not worth it to even try and pursue comfort.
im not your test subject. i do not exist solely to participate in your "revolutionary" research study that promises to cure me. im not a fucking lab rat. im a disabled human being who is going to be disabled for their entire life. i deserve respect, not to be treated like a specimen to be poked and prodded at. stop sending me messages asking me to participate in your study or essay or dissertation. im not fucking interested
hey, all the disability fetish blogs following me: youre fucking disgusting! unfollow me and go to fucking therapy. seriously what the actual fuck is wrong with you

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does anybody know of any spaces for people with ehlers danlos syndrome? i wanna connect with others who have it and (hopefully) learn more about ways to manage it from others who relate yk?
Photo ID: a tweet reading, “If you can’t see ableism, that’s probably because you’re participating in it.
"Love taking an 8 minute route that takes an abled 2 minutes"
Able-bodied people, this is what your world is like. In a new situation it's also usually impossible to even know an alternate route, so the options are like enduring the painful and dangerous illegal barriers or...going home. And for the people suggesting the op report these things- that's a great suggestion but you should also be aware of how often businesses, governments, schools flat out ignore concerns like this.
If it troubles you, I highly suggest making your own complaints every time you see something like this.
Do not shop at businesses that break the law. Do not let governments who deny disabled rights go unchallenged. Don't do nothing when your world is dangerous to us.
Just for once I’d like to tell the gate agents and flight attendants that my folding wheelchair is going into the onboard closet and not have them tell me there’s “no room”. Bitch that’s a wheelchair closet, not a “your bags” closet. Move your damn bags where they belong.
Ok, so according to my friendly aviation expert, this is a Big Fucking Deal. In fact, if an airline argues with you about putting your wheelchair in the wheelchair closet or even suggests there may not be room, unless there is already another passenger’s wheelchair in that closet, they have violated federal law.
CFR Title 14, Chapter II, Subchapter D, Part 382, Subpart E, Section 382.67, Subsection (e)
“As a carrier, you must never request or suggest that a passenger not stow his or her wheelchair in the cabin to accommodate other passengers (e.g., informing a passenger that stowing his or her wheelchair in the cabin will require other passengers to be removed from the flight), or for any other non-safety related reason (e.g., that it is easier for the carrier if the wheelchair is stowed in the cargo compartment).”
Source
This is hugely important because it means that if this happens to you, you should report their asses to the DOT. Why? Because these statistics are published every year for every airline, and the airline gets a huge ass fine for every violation. If we want to see change, we need to make airlines literally pay every time they treat us this way.
@annieelainey you should share this with your followers! This is important info!!
To my mutuals on wheels, print out the law before you fly and whip it out at the gate if they don’t accomodate your wheels.
Thanks a lot for posting this, bro! Flying while crippled is already difficult enough without people pulling this kind of shit. Also, make sure that if there is a piece of your wheelchair or something important missing off of it, that you make a big fucking deal out of it! I’ve had pieces fall off of my wheelchair and nearly lost a decoration I had on it that meant a lot to me because people were careless with my chair. Don’t let them mistreat your wheelchair.
Non-wheelchair folks:
Now that you know, speak up.
You never know when you’re going to see someone who needs an ally.
Shout out to disabled people who don't, can't, or shouldn't drive. You are not a burden, and even if you technically ""could"" drive you are not obligated to if it would be unsafe for you or others
Not being able to drive can be an inconvenience, but it is not a moral or personal failing. If anything, the failing is on behalf of society for not having better and more convenient public transportation for everyone

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shoutout to disabled ppl who HAVE to work. who have no other option but to push their illness(es) aside to the best of their ability because they need to survive. im going through the same. i love you. we deserve rest
if i'm being 100% honest I don't think anyone who isn't disabled tries to get disability i legitimately do not believe it. "x amount of people make false claims" no, x amount of people who make claims are declared not disabled by the government, an institution that doesn't give a shit about disabled people and wants to find any reason to deny us assistance. if somebody goes through the effort of applying for ssi, which isn't a simple process, just for the CHANCE to get a max of $794 a month (but likely less.) and not even be able to save that money up. they are genuinely struggling with something. nobody would choose this if they had other reasonable options