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#esp for those who are disabled
soothebellss · 1 year
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gentle reminder that your local pokemon center has free resources for pokemon healthcare, grooming, behavioral training, food, housing, etc for those who need it
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uncanny-tranny · 10 months
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I'm still thinking about how ashamed I was (and am) with being open about my pain because I am so young. It's so hard to feel worthy of having your pain taken seriously when the people around you insist that young bodies are always in pristine, untouched condition and that you must earn your pain through aging. Never is it considered that young people aren't lying or being a hypochondriac for expressing their pain.
Young people can be in life-altering pain. Young people can have debilitating pain. It doesn't matter what age it happens because pain doesn't discriminate. Complaining about pain and doing things to prevent needless pain aren't something you have to "earn" through aging.
If you want young people to be in less or lesser pain, then encourage them to do whatever they can to minimize it. Don't downplay what they're experiencing. Not everything is a lie, not every experience that is different than yours is exaggeration or deceit.
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todayisafridaynight · 3 months
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everyday i constantly think of masato's wheelchair and if that's his only one/main one no wonder he's so pissed at everyone
#snap chats#someone pointed this out to me like last year so im stealing it sorry cause I Think Of It Constantly#the handling of masato's disability will forever annoy me esp with how vague it is but esp his chair#one day ill draw masato with an appropriate wheelchair. maybe then he'll be happy for once#in a way i guess it could tie into how restricted or trapped he felt since the type of chair he's shown is more like. a hospital one#and not one youd really use as a regular user- like in that vein it is a bit of storytelling in that he can ONLY go out with help#since hospital chairs are SO much different from home chairs ESPECIALLY in regards to mobility and independence the user has#AND NOT TO MENTION HOW UNCOMFORTABLE THOSE CHAIRS ARE get his ass a proper cushion P L E A S E#like it portrays the idea that its unfathomable for him to go anywhere on his own and so in that vein . Interesting Storytelling#theres a lot of implications going on here if im so honest and again it makes for Really Interesting Story Telling#however i refuse to give rgg credit like that when it comes to disabilities. ... they havent earned that from me yet#see this is why the vagueness of his condition annoys me because he's shown to be independent enough to roll himself to his elevator#and presumably get himself dressed but he cant have a proper chair ?#because ik there are people who have expressed they have conditions where even writing is tiring#so if his condition was in-line with that and it was hard for him to push himself in his chair then i could buy it#obviously the issue lies with his lungs but i just want to know the full extent yk...#to wrap this up tho ive been thinking of character design in rgg and how we dont give credit to it enough#sooooo if i make a second post ten minutes from now thats why cause i keep forgetting to spam my thoughts on here LMAO#ok bye
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julesnichols · 4 days
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Wild to me to see a post about weed smell where people are getting dragged for saying they haven't done it before and it smells gross... bestie I have smoked and it smells absolutely fucking disgusting and thinking that while not having partaken isn't an inherent sign that someone is weird about drug users????
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mudstoneabyss · 1 year
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Kevin thanking Charles for not turning away from his face and not wincing but rather knowing he was the same as him & that kindness of that equivalent is rare is a metaphor for the way disabled people are often dehumanized and/or pitied and how uncommon it is to just be seen as a normal person like anyone else in this essay I will
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notjanine · 3 months
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people have assumed i’m queer my entire life, but nowadays i’m getting they/themmed on the regular and it’s fine, but it’s also interesting bc gender has always been the one fundamental aspect of my identity that isn’t constantly misperceived, so now it’s kinda. oh i am just not being Seen at all huh.
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barnbridges · 8 months
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twofers and autism moms on the venn diagram should be like, 80% overlapping and 20% out, but it's so rare to see anyone with actual autism or awareness of that it's a fucking disability hang around the mommy circles it disappoints me endlessly.
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benetnvsch · 9 months
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nothing is better than seeing all the quote retweets on That One Apology tweet by Dazai's eng VA lmao get fucked old man-
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vampire-nyx · 10 months
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I do think there is a very real issue and a conversation that needs to be had about this phenomena in disabled spaces where things quickly become disabled people with physical disabilities vs disabled people without physical disabilities (but even that isn't quite right, since that concept almost immediately always becomes visibly physically disabled people vs invisibly disabled people, physicality being irrelevant for the latter group)
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pepprs · 2 years
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covid is such an evil evil disease and an evil evil thing to live through lol
#purrs#this isn’t prompted by anything im just thinking about it. i hate that thisis what life looks and feels like now and it might always be thi#way. i hate that getting covid feels like an inevitability even though i wear n95s and don’t go anywhere but work and have basically 0#social life and have put my life plans on hold to wait for this thing to pass when it probably never will. i hate that lockdown was better#and easier than this in some ways because at least back then people were still scared and there still felt like hope and there was clear(is#) guidance and free testing and vax sites and whatever. i hate that free testing and public health dashboards showing covid rates and vax s#sites and all that shit have fucking disappeared even though the variants going around now are more contagious than ever. i hate the#mortifying ordeal of being the only person (or one of the only people) wearing an n95 and sometimes the only person wearing a mask at all.#hate that so many things have been lost and we are not taking time to grieve them or make sure that we are okay and will be okay. i hate#being scared every time i swallow. i hate how there is literally no way to tell if you will get long covid and no way to reduce your chance#of getting long covid or covid at all (aside from masks) just ways to make the symptoms less severe. i hate trying to bring people together#and stay away from people at the same time. i hate all the life that covid has taken out of me and the people i love even though thank god#know more people who haven’t gotten it than who have but actually that may not be true idk. and i HATE that because of covid and how#egregiously badly it has been handled everyone is just like.. perpetually tired and sad and we’ve accepted mass illness and death and#accepted that disabled people (esp those who are marginalized in other ways) are disposable when actually no fucking human being is#disposable and everyone should be able to live happy connected healthy lives and we could’ve ended this shit in EARLY 2020 without having t#deal with any of this absolute fucking NIGHTMARE. like god. i remember sobbing hysterically thinking we would be dealing with covid for 18#months and now we’re coming on 3 fucking years and lockdown is over but the danger is even worse than it was and like.. no one cares anymor#and it fucking sucks lmfao. i am so tired. i need to move out. and i miss my friends and i miss my life and i miss having fewer things to#constantly worry about and i can’t believe how good and simple life was before this stupid shit.#delete later#i wasn’t planning on going on a huge rant lol sorry it’s just what’s on my mind this morning
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matoitech · 2 years
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just recently typed out a big post abt why i especially dont like promare high school aus in particular and then deleted it cuz i didnt want 2 b a hater and i felt like i complained abt it enough. perhaps i shyould complain abt them More lest ppl think when i say i like aus i mean the common boring ones many of which i have a visceral hate inmy heart for (mostly the school ones coffee shop stuff is boring but i dont Hate it i jsut dont read it)
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clamorybus · 6 months
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i know a lot of people say things like 'if my post doesn't apply to you then its not for you' when they make advice posts, which i totally get. but when people make posts dissing picky eaters or adult cartoon fans or whatever, and other people point out that includes disabled adults, i feel like "oh i didn't mean them!" doesn't really work, y'know?
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johannestevans · 1 year
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i've been listening to a lot more fat liberationist stuff recently and like...
so obvs i already had some backing in a lot of the basic theory, stuff like institutional anti-fatness in medicine, fashion, travel, etc, but like
so as a really thin guy who's always found it impossible to gain weight, its been unbelievably emotionally and mentally liberating to hear people talking really casually about the disability that's associated with thinness
so like being really thin, you lack additional joint and bone support - if you fall, you have less padding and less STRUCTURE to protect your bones from breaks and fractures, right?
obvs theres plenty of fat people that do have issues with bones and joints, im not saying thsres not, its just that normally i feel like im the lone person saying "being this thin is bad for me and is part of various health problems i also have"
and idk its just like. my whole life i was such a sickly child lmao
like i couldnt stand for long periods except "long period" would often be like. any period. i didnt understand how my peers were just standing for so long and just weathering that, bc to me it wasnt possible at all - i breathed badly, my joints were fucked etc
and looking back and realising as i get more disabled like the extent to which i was similarly disabled in my youth, and how i lacked the language to verbalise or sometimes even recognise my own pain and struggle
but also like
the treatment of me as so evil and lazy because i wasn't exercising, or because like. a PE teacher would pick me out as an example because i was so thin, and then be furious that i wasn't remotely physically fit, and that i was disabled
i remember multiple times esp from cis female teachers just. frothing rage at my diet and the things i ate, or when i wrinkled my nose at talk about diets, bc i was so thin so i had to be doing The Right Things, and if i was that thin and doing bad things i had to be punished
and its bc a lot of these ppl thought of fatness and being fat as a punishment, a target for abuse that people deserved, and bc i was a young disabled trans guy like. i deserved punishment for my laziness and nonconformity, and it became a lot about my weight
like expressing that i wanted to gain weight, that i was cold all the time, that i had no energy etc, that eating was hard but that i enjoyed food, all of that was met with such fuckin aggression and really sharp policing, esp from PE teachers and esp from women
and obvs all that is to do with the way that diet culture particularly targets women and those perceived as women, and the desire to engage in lateral violence to police others into complying with gender roles etc as they were upholding them
but idk like. fat liberationist politics is imo inherently tied up with disability liberation, because of the way that "health" is weaponised as a symbol of being good or deserving, and how fatness and disability are both used as targets and symbols of evil and punishment
MOST OF ALL for fat & disabled people
but for nondisabled fat people disability is often threatened as punishment - if you don't become less fat, you'll (deserve to) become disabled
and for disabled thin people, if you don't act less disabled, you'll (deserve to) become fat
and its not a punishment to be fat or disabled or sick. its just how some people are. its not BAD to be this way - and what makes things hard for us is not something inherent to the badness of our bodies, but instead the lack of kindness and accommodation anybody is willing to extend to them
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grotesque-grimoire · 4 months
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Looking for active witch blogs that post:
🕯 Altars
☠ Baneful Magic (curses, hexes, jinxes, etc.)
💸 Budget / Poverty / Struggle / DIY / Upcycling Witchcraft
📖 Magical Books (pics of grimoire pages, flip-throughs, book recs/reviews, etc.)
💲 Money, Business, & Prosperity Witchcraft
💀 Necromancy, Death Witchcraft, and/or Cthonic/Death Deities (also funerary stuff, medical examination, etc., love that stuff)
🌿 Practical & Responsible Herbalism (gardening, cultivating, harvesting, foraging, herbal remedies, recipes, salves, ointments, etc. but no anti-science, anti-medicine, anti-allopathy shit)
📝 Sigils (free to use, preferably)
👻 Spirit Work (esp. animal spirits, dryads, egregores, genus loci, gorgons, & mermaids)
🥄 Spoon-Conscious Witchcraft (for those who are disabled, exhaust easy, etc.)
✨ Things relating to: Santa Muerte, Artemis, Serket/Selqet
🦴 Vulture Culture (responsible)
Reblog or send me an ask if you think your blog might suit my taste. Disclaimer: not Wiccan, not Pagan, not Heathen; just a witch who's curse-positive, eclectic, & agnostic.
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lavend-ler · 9 months
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tips on how to write cane user Neuvillette from a crutch user
Neuvillette uses a cane - and that's amazing! but increasingly I got worried that the portrayal of him being a cane user could be based on harmful stereotypes. hence I wanted to make a list on tips I can give as an irl crutch user
DISCLAIMER - this is in no way exhaustive list and I am no end all be all authority on this. I'm just a disabled person in fandom who is tired of ableism. of course this list can be used for other disabled characters but I esp wanna focus on Neuvillette (cause I love him)
Neuvillette is an occasional cane user (just like me) and that's totally fine. he doesn't have to use it all the time to be "disabled enough". he probably uses it during the days he feels worse
he holds cane in his right hand - that means it's his left leg which needs support (again, just like mine!)
a lot of disabled ppl are prone to the changes in the weather. I think it'd be interesting to keep in mind esp in Neuvillette's case
as long as we don't have the canon confirmation on what is Neuvillette's disability, all hcs are fair game. personally bc I relate to him I hc him with my own disability - arthritis
don't be afraid to portray him using his cane in combat. mobility aids are often used by disabled ppl not only as a support in walking but also in every day things. for example, he could be pushing buttons with it or helping himself while walking the stairs
bend the ableist stereotypes - make him use his cane and be badass with it. esp since he proudly uses it during his burst
canes make ppl more visible. don't fall into ableism and make characters only care abt Neuvillette when they notice him using the cane. if u choose to do so, make Neuvillette remark back, noticing how ppl treat him differently and unfairly
do not make jokes abt his cane. I have already seen ppl make jokes that he's an old man who needs to use the cane. it's disrespectful and unnecessary. don't bring up him being a cane user only when u talk how he's old
canes are very personal. even if others offer help or to hold it, Neuvillette would be against it
on that note DO NOT MAKE OTHERS CHARACTERS TAKE HIS CANE esp if u want to treat this as silly fun or even worse, romantic. Neuvillette's cane is his business and any character taking his cane from him would be extremally disrespectful
Neuvillette might have to take breaks between longer strolls to sit down and regenerate. again, sth that happens to me a lot
tho every character in Genshin has to be quite active, remember to portray Neuvillette to be relaxing too! he can be badass, active and strong and that won't make him any less when he's relaxing. I absolutely suggest u portray how he relaxes after the day and how he takes care of himself. maybe a calming tea or some ice packs - those are definitely great options for chief justice to relax and ease his aches after an eventful day
HERE is another post that focuses on more on experiences of mobility aid users. I find it very relatable and useful, it's a fantastic further read
hope these will be helpful for u! ablebodies please don't derail. other mobility aid users, feel free to add more things to the list <3
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thatdiabolicalfeminist · 10 months
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We all deserve:
consistent access to enough food
food that meets our nutritional needs
food that doesn't cause pain/discomfort/harm to the individual eating it (allergies, medical restrictions, etc)
food that meets our religious/cultural needs
food that doesn't cause undue burden to prepare (esp not so much burden that it regularly keeps us from eating or damages our health)
food that no one was harmed or coerced to make or grow
a variety of foods
that we enjoy eating
How many of these points are attainable for the average person under capitalism? How many for poor people? For poor disabled people? For poor people who come home from low paying jobs completely exhausted and unable to consistently do more than a few minutes of food prep, or any at all? For prisoners or those living in medical institutions?
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