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#work and disability
candlecafe · 4 months
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Sorry, I haven’t done my work, yeah, I’m in spoon jail. Yeah, I was in really bad spoon debt, and I stopped paying my spoon taxes. Yeah, I can’t do anything until I gather enough spoons to pay my spoon bail.
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saszor · 2 months
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gay people real 🌝
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trans-cuchulainn · 8 months
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wish abled people would understand fluctuating disabilities more. i told my boss my knee was better today than friday and she's like "I'm glad it's slowly getting better" but it's not Getting Better, it's just having a good day (and tbh it's worse now than it was when I said that) and tomorrow it'll probably be unable to bear my weight again. like. stop thinking of these things as a straight line progression because they're not and I'm tired to having to explain every bad day like it's some bigass new problem when it's just. the nature of these things
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lokilysolbitch · 5 months
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i've said it already probably but ppl who don't use mobility aids. especially doctors. stop trying to get rid of other ppls mobility aid. stop making that a priority. stop it with the "we gotta get you off that [mobility aid]" "you shouldn't need to be using a [mobility aid]" "let's focus on getting you to where you don't need [mobility aid]" "a [mobility aid]? but have you tried [herb]/[medicine]/ [exercise]/[facebook hack]/[pseudoscience]/[meditation] instead?" "but you look old/cringe/weak/sick". shut up
i don't know why so many of y'all think my end goal is to stop using the thing that helps me. and i KNOW most of y'all wear glasses or contacts but you're not running around trying to find the solution to make you stop needing them. so quit doing it with every other aid just because it reminds you of old or sick people.
especially bc most of y'all don't want to have that reaction when it comes to chronic pain, fatigue or discomfort. i say "my joints hurt" you say "oh well :/". i say "i feel lightheaded all the time" you say "just push through it". i say "my stomach is at least a 7/10 on the pain scale every day" you say "are you sure it's actually that bad? maybe you're exaggerating".
but as soon as i pull out a cane, or a shower chair, or a spinny chair for when im cooking in the kitchen, and i say "finally, im getting really good help!" . that's when you care. and all you want to do is take that away as soon as possible.
you just don't want to fucking see disabled ppl be disabled.
you don't want to have to look at it. you don't want to have to listen to it. you don't want to have to be reminded of it.
but too fucking bad !! i don't care !! im naming and decorating my canes !! they will be the loudest part of my outfits !! the same will go for a rollator if i'll still need one in the future !! i'm going to talk about how i'm disabled regardless of if anyone else can hear me !! because i am !! why should i hide just because YOU don't like it !! close your eyes !!!!!!
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personishfive · 1 month
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in which dialogue is exchanged
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the other thing about being disabled in academia is everyone is like "yeah we can't do much about the buildings they're old :/" as if "old" being a synonym for "inaccessible" isn't just a constant reminder that the people who built the school did not imagine that someday someone like me might study there
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wild-neko · 7 months
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disabled people: we are still dying, can you please just wear a mask to the grocery store and doctor’s offices so we can live
conservatives: no, die or stay inside all day, no one cares
leftists: no 🏳️‍🌈✨💖
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furiousfinnstan · 2 months
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Crowdfunding yet again 🫠
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hello I will try to be brief,my sister is disabled and recently she got horrible news from her doctor that her reflexes have gotten worse,which means she will one day probably become paralyzed unless something is done(also her chronic pain is pretty severe rn which is another bad sign).now they want her to do a bunch of exams + physical therapy+ maybe new medication??we are looking at a bill close to 800€ tho honestly I dont know what's going to happen.the first paragraph you see is nothing but blood work and allegedly we will be able to get those for free so that's a relief.But I'm convinced thats not going to be all I'm scared for what's going to happen to her,I'm scared she will need to have surgery.also long covid is still fucking with me so yeah I'm don't think I will ever find work at this point🫠but who knows maybe I will be fine one day.I'm going to ask for 1200€ just to be safe tho dont be surprised if the amount rises or drops because I again I don't know what to expect with this,the extra money is in case we do need to pay for extra exams,blood work or bills etc
Goodbye for now 15.feb.2024
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tam--lin · 1 year
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The thing is, you don’t have to have a diagnoses to make simple “unmasking” changes that make your life easier. You don’t even have to self-diagnose! You are not appropriating anyone’s culture or struggles or hijacking anyone’s movement by allowing yourself to sway in line at the grocery store or buying a weighted blanket or using study or household hacks intended for people with ADHD. If you start favoring the needs that make your brain and body unique over the arbitrary norms of society, you’ll be better off, and you’ll be expanding the norms. It’s a win/win.
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sydosargent · 5 months
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Disabled people are allowed to eat what we want btw. Even if we eat it badly or messy. Mind your business.
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phoenixonwheels · 2 years
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Ableds be like, if I eat this diet/do this exercise/wear or don’t wear these clothes/live this lifestyle I’ll never become disabled!
Buddy have I got some harsh news for you…
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maxpawb · 3 months
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finally made a ref for my side fursona/truesona yippee
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teacupsandcyanide · 1 year
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Something I miss from earlier eras of the creative side of the internet was things just being unabashedly low-budget. Just all unashamedly amateur, unprofessional, ‘I don’t own a good camera but I have a story to tell you’, ‘I can’t afford a good mic but I have a song to sing for you,’ ‘I don’t have any kind of background in editing or lighting and I only just picked up this guitar last Tuesday but here’s an entire musical me and my friends wrote about our favourite book, we filmed it on a potato and put it up on YouTube in ten minute segments because we thought it was pretty funny.’
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chronicpaingirlie · 4 months
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me walking without a mobility aid: this is fine i literally don’t even need a mobility aid
me within a minute of this: unrelatedly why do my legs hurt so much and why am i so exhausted
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chaos-and-ink · 21 days
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Nothing About Me Is Straight
I'm making stickers based on my chronic illnesses for my final project in my art class. This is the first one! If people like them I'm thinking about adding them to my shop in the summer when I have more time.
Funny enough I killed my wrist and fingers trying to draw this. ouchie i need to buy some splints soon
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diadraws · 6 months
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im finally done moving into my stupid new apartment so i drew some symmetry icons of evil fucked up creatures to celebrate
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