Chronic pain pisses me off cause I'm not even incapacitated for like a cool or badass reason instead my body is throwing the world's biggest temper tantrum because it's raining outside
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Chronic pain pisses me off cause I'm not even incapacitated for like a cool or badass reason instead my body is throwing the world's biggest temper tantrum because it's raining outside
unpopular opinion i think disabled people should be able to struggle with silly things an complain about it without someone just sayin "agh y'all can't do nothing" sometimes I don't want to talk about how i have problems sleeping cause i wake up chocking on my own vomit/regurgitation or acid, sometimes i just want go talk about how playing dmc with hypermobile fingers is hard as fuck or how adhd makes difficult to choose wich type of coffee i want and that's ok
by the way...
PSA!
please do your best to not express disgust when a hypermobile person... exists. like, i'll bend my fingers weird, and the people around me will writhe and gag in disgust. referring to it as "body horror" is the worst part. it's not body horror. my body isn't horror. my body is a part of me.
yeah, it's a little freaky when you're not used to it, but please do your damnedest to keep it to yourself. it's incredibly humiliating to be on the receiving end of that sort of thing. it makes me feel like a monster or something less than human. be kind to those that aren't like you. that's the lesson at the end of the day, for all things.
thank you for your time 🙏
People take the word ambulatory wheelchair user, and say it means exclusively part time wheelchair users and run with it.
I’m an ambulatory wheelchair user. But I’m not a part time wheelchair user. I use my wheelchair EVERY SINGLE day. That means that I’m not a part time wheelchair user, because I use it more than part time. A lot more than part time.
There seems to be this new rhetoric, that ambulatory = part time. And for most, this isn’t the case. Ambulatory does not mean part time, it simply means that you can walk.
I can walk around my room unassisted by any mobility aids. I cannot walk to the lunch room which is literally up the hall without a mobility aid. I’m almost a full time crutch user, and I’m an ambulatory wheelchair user.
I am not a part time mobility aid user, and I hate that people have come to the “agreement” that ambulatory means part time, when that is quite literally, not true.
It’s okay if the only thing you accomplished today was keeping yourself alive. Existing with a body that constantly malfunctions is exhausting. You don’t need to ‘earn’ rest. You already deserve it.
- reminder to myself this upcoming week.
me, cracking and popping my everything all the time due to the fact that my joints are weird: waow... just like ben reilly...
Hello dolly!! I really enjoy reading your fics so much
May I request a sevika with a plus sized reader fluff? Where reader is doing yoga surprising sevika with their flexibility for the first time?
Hi! Thank you!! 🫶🏻
I have EDS so I’m also super bendy! I’ve stiffened up a bit now but when I was first diagnosed (over ten years ago) my party trick was to do the ‘Dancer Pose’ (Natarajasana) and put my foot on my head!! (Defs permanently messed my hips up but it was funny at the time 😭)
Wife!Sevika x Reader - Steady
Summary: Sevika comes home to find her wife practicing yoga. What starts as surprise, quickly turns into pride and admiration.
silly ableism is my hypermobility making me unable to walk because my legs hurt, but if I use my cane my wrists start hurting instead, and if I stay in bed my back hurts too
This is silly ableism!