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#because yeah i have physical disabilities
sir-ghost-the-green · 4 months
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List 5 things that make you happy, then put this in the askbox for the last 10 people who reblogged something from you! get to know your mutuals and followers 💜💜
This is really sweet! Will do! This isn’t going to be in any specific order lol. Things that make me happy:
- My dog bc he’s my world honestly. I know he’s not a thing but I couldn’t talk about what makes me happy and not include my bean, it simply wouldn’t be complete.
- When I’m asked about one of my fixations and the person I’m talking with actually cares and wants to listen. Or asked about anything, really, I like to talk lol.
- The English language in just about every form; reading, writing, audio, spoken in person, all of it.
- Accessibility!!!! My gods I cannot tell you how happy it makes me when places and things are accessible for all sorts of people. When I and people with disabilities far different than mine are all being properly accommodated it fills me with joy.
- Making things. I joke that my hobby is picking up new skills, but that’s really because for me making something new with my own hands and skills is such a significant source of happiness that it’s hard not to constantly pick up new projects.
Thank you again for asking me Magpie!!
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ciderjacks · 1 year
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the thing is whenever I see discourse on who can “really” use disabled accommodations coming from people with invisible disabilities I’m like. Ok. You guys need to realize being physically disabled does not automatically equal “I get access to all the cool disabled stuff now”, if you don’t actually need it, don’t fucking use it. It doesn’t matter if you’re physically disabled or not, if you don’t need the big bathroom or the special seats or whatever, then don’t use it bruh.
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thedrotter · 17 days
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look i know this month has been crazy already in what has been going on for me BUT IT GETS CRAZIER... I got to finally have my constant pain I've had for two years diagnosed... I have fibromyalgia lol i have a chronic illness??😭😭
tbf it doesn't change anything i was already coping with these pains because I've been sitting with em for 2 years i just have anti depressants now but you know what has changed... my character lore GOT SICK AS FUCK!!!!!!!🦅🦅🦅🦅 (lighthearted)
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obstinatecondolement · 7 months
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It feels like every day I read attempts to debunk the social model of disability that fundamentally misunderstand what the social model of disability is and who the people who developed that model were, including what the nature of their disabilities was, and I want to scream.
But I don't, because yelling at people on the internet is basically pointless. Instead I check to see that I'm not mutuals with whoever reblogged said misunderstanding and vague about it.
#'but [x impairment] would still exist and have [y implications] even if the world were completely accessible!'#okay well yeah but equating impairment and disability is explicitly the opposite of the social model of disability#the union of the *physically impaired* against segregation who developed this model#*were* by and large privileged in ways many other disabled people are not‚ yes#mike oliver who wrote the fucking book on the social model of disability#(social work with disabled people‚ published in 1983)#was a white man with a phd who pioneered an academic field‚ for one#and there *are* criticisms about the limitations to a purely social model of disability to be made#but like... our pal mike oliver was also a wheelchair user who broke his neck in a swimming accident as a teenager#which caused paralysis that affected his upper and lower body#not a clueless 'physically abled' autistic who didn't understand how physical limitations work#he lived the first 17 years of his life as a physically abled person#so I think he was aware of the difference between what his body could do before and after his accident#and like 'disability is socially constructed'#is not saying that differences between people and what they are able to do or do easily do not exist??#my eyesight is so bad that if I could not access corrective lenses I would be functionally blind#and even with glasses my myopia and astigmatism cause a lot of tangible effects on my body#e.g. migraines‚ eyestrain‚ so many floaters that even looking through pristine glasses is like the lenses are scratched to hell#but my eyesight is not considered a disability#because the accommodations that enable me to participate in society fully in this area are so standard as to be invisible#can I magically see without corrective lenses? no#does wearing glasses not being considered a disability mean that I do not get migraines and eyestrain? no#so the arguments the thing I am vaguing are trying to debunk are not what is being argued!#well seems like I screamed about it after all#oh well
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atopvisenyashill · 2 months
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the sociopath thing does irk me i will admit and some of that is i just feel it’s an inappropriate word to be using in the year 2024 (it's not a nice word i don't give a shit about its literary or metaphorical merits, of which it has none anyway!!) but i also think it’s functionally useless because sometimes people mean “this person has a scary disorder” and sometimes they mean “this person is ontologically evil” and sometimes they mean “this person is ontologically evil and i’m sad about it, how tragic” and it’s like. what are we talking about here. you can’t just be like joffrey/criston/ramsay/tywin/saera/cersei/whOever is a sociopath and expect anyone to think that’s a satisfying answer for why they act the way they act. “gregor clegane is a sociopath” but WHY. “no i mean he really does have like sociopathic disorder” that’s not a diagnosis and the range of things he could have that would make him display “sociopathic behavior” is SO VARIED. just say what you MEAN.
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amokslime · 6 months
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About the whole ADHD "finding a way to motivate yourself without using the stress of impending deadlines" thing:
I hate to say it, but learning to be nicer to myself changed a lot of that for me. I really truly hate to say it. I'm sorry to be the bearer of bad news but you gotta find a way to be nicer to yourself inside your own head, in whatever way works for you. I know it sucks so bad to hear.
The other thing is, if my brain is really refusing to tackle a task, often times the main thing I'm feeling is confused and understimulated. Which leads to me sitting there with the jeopardy theme song playing in my head, and then I unconsciously gravitate towards something that's more stimulating and therefore easier to wrap my head around. So overstimulating myself in some sensory way helps me be less confused about what I needed to do. Everybody's brain is different, though.
And uhh the other thing that helped is concerta, and listening to my body, and working on not being so ashamed when I failed. Which means you will probably have to fail a little bit unfortunately
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heir-of-the-chair · 11 months
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You know, when they said “you never stop learning things about yourself” I don’t think they meant five consecutive years of having a new identity crisis.
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brinnanza · 3 months
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I think it's important to resist the urge to pathologize ultimately harmless behavior like maybe you can trace it back to its parent disorder but if it's not harmful to you in any way that isn't a symptom it's just a trait
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gemglyph · 4 months
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Hello everyone! Sorry for sort of disappearing. I’ve burned myself out and have received sort of upsetting medical news. Anyway, steadily working on Martyr. It’ll be out when I accomplish it.
I love and appreciate all of you
Thank you
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yonpote · 5 months
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ok i literally only did two prompts but thats it for now i will get to the ones in my inbox tomorrow ✌️✌️
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trans-axolotl · 1 year
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having a lot of thoughts about eating disorders + how some of us end up developing chronic illnesses directly because of the physical effects of our eating disorders and how Cruel doctors can be about that and just trying to untangle so much shame and blame from that experience rn
#personal#vent#eating disorder tw#disability#idk. i don't quite have the words for this right now but#had another meeting with my doctor where they said yeah its your fault that you are now physically disabled for life#(literally i was chronically ill and physically disabled before i even developed an eating disorder because of CAH and comorbidities but#(they love to ignore that !)#which is like. i do not tie any morality to health and it should just be#a completely neutral statement. that my eating disorder caused other physical complications#they said i'm going to have orthostatic problems the rest of my life.#'since your gastroparesis was caused by your eating disorder that means there is no point in treating it'#which is so funny bc literally every time i see her my dietitan wants me to get a feeding tube! lmfao!!!!#i am actually doing pretty well in recovery in terms of meeting my energy needs through food. but i stopped being able to orally supplement#so my dietitan wants a tube for ARFID nutrient reasons. supplemental nutrition etc etc. and she thinks it will help gastroparesis symptoms#they also think i have osteoporosis and want to test me for that#when i had to use forearm crutches/ wheelchair because of physical ed complications doctors were SO fucking rude even though they were#the ones PRESCRIBING IT!!! like!!! you all are the ones telling me i HAVE to do this!#idk i also have a friend with permanent brain damage. from seizures in the refeeding process#and her doctors are so fucking rude to her all the time.#it makes me so mad
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one thing abt being disabled/chronically ill that some people don’t get is that sometimes body maintenance that ensures you have the absolute minimum amount of function can also be something that takes away a lot of control and autonomy. you can argue till the cows come home that making those decisions to try and help yourself (or realistically to try to make sure things aren’t worse than they already are) is something that exhibits control and autonomy and stuff, but they can be so limiting in practice because they’re things that take up so much time but have to be done to do anything else
#i have to sleep a lot. i’m at the point where functioning requires 8 hours of sleep if not more#I should probably be getting 10+ but i’m a student and i work so 8 is the minimum. but then also getting ready for bed is a whole process s#the whole thing can take 10-12 hours depending how much im sleeping. just to make sure i can do anything#that is time in my day i cannot use for anything else. it’s not ‘oh but i can push through it’ because i can’t without spending the next da#lightheaded and nauseous and vaguely dizzy and with such intense brain fog I can’t think with my fatigue so bad i genuinely don’t know how#get myself to work a lot of days. my abled peers don’t have to deal with this at all. they have unlimited study time if they want to#and yeah it is a choice i’m making that’s true i could just not do. except i would lose my job and fail out of college because i would not#be able to get to classes or do my homework or think. but being told ‘but you are making choices about your life’ when i have lost so much#of what i used to be able to do because i am spiralling down and continuing to get worse is so.#literally last year i would wake up at 6:30 and then go to school till 3 and then go to my internship until 10 and get home at 11 and be in#bed anywhere from midnight to two in the morning and then wake up the next day and do it all again. i graduated with a 3.9 gpa and made it#into my top college while dealing with my cancer symptoms and then the two surgeries about it#but now i lose half my day to just making sure i can get out of bed. i can’t go anywhere because my body is physically too exhausted#any extra time goes into doing homework or occasionally time to myself#not decimating my health by doing minimum body care responsibilities isn’t freeing. occasionally i have a good day which is freeing but tha#usually goes into just. other things outside class or work or eating. I don’t go do something for myself or go do something fun on good day#because I still can’t. good days just mean i don’t want to lie down on the pavement when i’m going somewhere#I just. I don’t magically have control over my life because i try to get enough sleep. i lose half my day to doing that and ultimately it’s#just a bodily function that would have to happen anyway#this is a vent post im just having a really hard time right now because it feels like im in exponential decline. it was nowhere near this#bad last semester. my grades are tanking and i have no free time because anything outside of sleep is either work or school#vent tw#yall can rb this just ignore my tags completely#disability#chronically ill#i keep trying to explain to people how pots works because that’s all logical but there’s no way to explain what it’s doing to my body or ho#i feel all the time. the last time i felt this bad was when i had a bad flu or immediately after surgeries because i don’t react well to#anesthesia and always come out of them feeling like shit. and now i just feel like this all the time and it’s only getting worse#I can’t even stay up late anymore because my body feels like it isn’t counting the sleep even if I get 8 hours#I can deal if I have a free day the day after but that just leaves Friday and Saturday nights and I usually still have to do homework
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lesbians4armand · 2 months
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its such a funny feeling that for so long i’ve denied being disabled. ableism runs so deep in our society that as long as i can walk and work i didn’t consider myself disabled despite literally being disabled. fuck this capitalism shit
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skrunksthatwunk · 2 months
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"i'm not disabled" followed immediately by "i've got bad knees and a bad back" is certainly something to read 🤨 you know it doesn't have to be cripling for it to count, right...? it's not normal to be in pain after 15 minutes of standing. ableds can stand for, like, an hour at a time before they need to sit.
i know! i appreciate the concern, but i uh. dunno lol. genuinely i don't know. but i included the afaik ("i'm not disabled afaik" was the original phrase, though i'm not like mad at you for excluding it or anything) because i'm well aware that it's a possibility. it's hard to explain but there's a lot of little things that don't add up to much but are like. noticeable. like i would prefer to do most things sitting, if i could, as a matter of comfort. it would be easier for me. and walking isn't as bad as just standing. i've never been great at taking care of my body, and this has only gotten worse with time. it's hard for me to know what i should read as necessity and what i should read as preference, and how much weight to put on said preferences. like you said, i know it doesn't need to be "if i don't sit down i'm going to collapse" or anything, but where to draw that line between Definitely A Medical Thing That Affects Me More Than Other People and.. not that, i'm not sure. i kinda just thought i was a persistently slightly tired and low energy person, but it doesn't seem bad enough to be chronic fatigue, so...? is it related to the half-diagnosed. idk it's complicated depression (and yes in hindsight i probably should've counted that as disabling but whatever)? idk it's not a rabbit hole i've explored much at all is my point. but i know it's there and uh i guess this was sort of validating in a way anon so.. yeah? yeah👍
#also in reference to the pain after 15 mins of standing thing it's.. usually closer to discomfort than pain? but it's not Not pain either#it's often more like 'oh i should sit down. i wanna sit down. i should sit down' and it's not that frequent but it's like a status effect#and the frequent reminders are only after like 20-30 minutes#sometimes i don't even notice it and sometimes (if i'm bored lol) i'll notice it a Lot#this is not helped by my body being.. iffy at telling me what's going on. it's always too much or too little input with this guy#ahh that rascal. anyway#listen anon 1) uh sorry for going off like this idk if that's like. socially appropriate or whatever but i'm doing it anyway 2) if you've#got ideas i'm all ears. like off the top of your head not like. im not asking you to do research for an internet stranger ok#plus it feels weird saying i could be disabled when i have no idea what it would even be. i mean i think i'd believe someone else if they#said that but it's a classic rules for me and not for thee situation. still working on that#point is i got brain gunk for sure i just don't know how much of the body gunk is because of the brain gunk or smth else#like the possibly-probably autism definitely affects me physically i just don't know exactly what to do with that information#like. am i exhausted bc i'm overstimulated? is it the burn out? or is that a separate thing? or are they working together? etc#anyway yeah got caught vagueposting about my symptoms here's the deep dive no one wanted. for self indulgence purposes :v#no but i think about it a lot with posts like this bc i mean. would an able bodied person react THAT strongly to finding out shower stools#exist? probably not. but who knows for certain#....coming to the conclusion of. probably. maybe. but in what ways specifically? uh. i dunno. i just got them heavy limbs#might be a thyroid issue now that im looking into it. but again this is Not my area of expertise
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void-tiger · 2 months
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…wHY do y’all feel the need to mention where someone’s at when they’re not around! Sure I have a crush on that idiot but I’m never going to admit to it, and actively avoid bringing them up myself ‘cause it’d feel like a freudian slip and it’s not my business anyway.
How often do I even come up in y’all’s home conversation. Is it out of pity? Or is this idiot just as insufferable as I am to my friends who are WELL AWAY from this and therefore Safe to repeatedly try spring-cleaning my demiromantic acengst with.
Are y’all pressuring them about me, too, or has that FINALLY, finally eased off.
(And what value can I possibly have, anyway. I’m unemployed and just shy of a shutin from severe anxiety/moderate depression and cptsd, adhd, and a smorgasbord of muscular-skeletal issues that just keep creeping up and staying and moving the goalpost to even TRY getting a job. The idiot has other friends when they have time to spend on them. All I am is stubborn enough to stick around and wait if I’m not actively being chased off IF the other party seems to really want that connection.)
#tiger’s roar#i am pathetic#and it’s hard to feel Good about being moved out#when I CAN’T work/keep a job. and how many credits I have to take to keep my scholarship makes trying to get a part time job Impossible Too#I’m doing this on student debt#and my parents won’t just Stop calling me spoiled apparently out of envy#that they’re able to spot my deposits and rent for the 2 months before reimbursement#and cover getting things like cooking utensils and used furniture and cleaning supplies#even though 2/3rds of what I have I either bought/kept myself OR are things they don’t want anymore#if anything. it should be a victory that they CAN provide this for me#where their parents’ couldn’t or wouldn’t#sure I got to move out whereas they immediately married ‘cause a kid was in the oven and the judgement that came with that#but they also weren’t chronically ill to the point of disability#and the chances of me marrying? almost zero. because I’m asexual and kiss repulsed and demiromantic#…sure I’m pretty sure my crush likes me back. and despite what happened last year their family really seems to like me#but even if they felt they did have the time and energy to just. ask me out? or hang out like we both seem to want?#I don’t think I’d ever accept that I wouldn’t just. drag them down with my stupid health#and even WORSE: make them feel sensually neglected ‘cause I can’t even think about kissing without basically gaslighting myself.#…friends can be supportive and physically intimate with hugs and whatnot#but me as a girlfriend? HA. I can’t give someone ‘enough’ without making myself feel utterly awful#and yeah. there’s a grief with that.#I’ll…try to let it be someone else’s Choice. not make someone else’s decisions for them#…but.
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fefairys · 1 year
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see but if juice and i were fictional characters everyone would be all "omg theyre so toxic yaoiyuri theyre so insane i love them" so i think we are cool 😎👍
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