incredible 10/10
everyone gets to observe my crutches
comfort items are important. whatever that means for you, do it.
me carrying a stuffed animal around while being disabled is not "infantilizing disability"
I am an actually disabled person who carries a stuffed animal as comfort bc disability is hard
what's "infantilizing disability" is assuming that just bc I carry a stuffed animal I'm not capable of making decisions for myself. or that having a stuffed animal makes me a less serious, adult person than you are.
what if i only drew disabled characters forever lmfao
fanart? yeah but theyre all disabled now.
oc? yeah theyre all disabled too.
oh youre sick of seeing disabled characters?? too bad im sick of not seeing any.
gonna fucking roll a dice of disabilities for every drawing out of spite. :)
THIS IS GENIUS WHY HAVE I NEVER DONE THIS
slay ty to ur partner for accidental allyship
People who spend a lot of time in/on bed, I have a recommendation for you... Go to some big and cheap store like Kmart and get yourself a kids activities tray!
My partner got this for doing crafts on the couch but we've repurposed it to be a writing surface for my bed-rot days. It's not perfect (I'd prefer a surface a bit higher, and it squishes these thicc thighs a bit) but it's a pretty good stop-gap for $10-20
STUNNING CRIES
Bloom
I’m practicing painting and I’ve been in a winx funk lately
really struggling with this atm.
ive lost all the strength i fought so hard for the past two years. it doesnt seem fair that it can all be taken away so fast.
im exhausted. trying is exhausting.
disabled consistency prt. 2 prt. 1 here (u dont need to read it to understand this post)
what happens to consistency, to habits, when you have a dynamic disability?
i want us to understand the differences between having a consistent body and having an ever changing one. sometimes you could be so healthy you are working/studying, exercising a few times a week, socialising, and independently caring for yourself. but other times.. you’re bedbound? can’t even shower and brush your teeth twice a day? can’t keep up with texting your friends or social media? what habit is surviving that.
you work so hard to build habits and follow routines you and your doctors have set, and then you achieve it, but then it all gets taken away in a flare-up. you wonder what the point is. its a constant vicious cycle. even abled people know its hard to build habits. it takes time. and you might not have that time.
for abled people, theres no time limit on building a habit. they might have a goal in mind of when they want to achieve it, but theres no actual clock ticking in the background.
for me, and for other dynamically disabled people, we are on a time crunch. you may not be aware of it, but you are. it’s always a race to get things done while you can, build those habits and routines and get consistent and get your life together while you can. because even if you’re not thinking it, you are living on a countdown until your next flare-up. until the next crash, the next time you lose all your progress.
and that cycle, is exhausting. it’s like building a sandcastle right on the shore. you build it and you get to revel in it for a second. then it’s gone. there may be a little bump in the sand where your hard work had just stood, but essentially, you are starting from scratch. while the abled people are up the beach a few metres and their sand is perfectly wet and perfectly dry and the waves never reach it.
then those same people, tell you to just keep building. “eventually you’ll get there!” “keep trying!” “habits take time!” they say. but how? there will always be another wave.
understanding this difference in experience is so important if you want to understand why you can’t just tell a disabled person to form habits or be consistent and expect results.
disabled consistency prt. 2 prt. 1 here (u dont need to read it to understand this post)
what happens to consistency, to habits, when you have a dynamic disability?
i want us to understand the differences between having a consistent body and having an ever changing one. sometimes you could be so healthy you are working/studying, exercising a few times a week, socialising, and independently caring for yourself. but other times.. you’re bedbound? can’t even shower and brush your teeth twice a day? can’t keep up with texting your friends or social media? what habit is surviving that.
you work so hard to build habits and follow routines you and your doctors have set, and then you achieve it, but then it all gets taken away in a flare-up. you wonder what the point is. its a constant vicious cycle. even abled people know its hard to build habits. it takes time. and you might not have that time.
for abled people, theres no time limit on building a habit. they might have a goal in mind of when they want to achieve it, but theres no actual clock ticking in the background.
for me, and for other dynamically disabled people, we are on a time crunch. you may not be aware of it, but you are. it’s always a race to get things done while you can, build those habits and routines and get consistent and get your life together while you can. because even if you’re not thinking it, you are living on a countdown until your next flare-up. until the next crash, the next time you lose all your progress.
and that cycle, is exhausting. it’s like building a sandcastle right on the shore. you build it and you get to revel in it for a second. then it’s gone. there may be a little bump in the sand where your hard work had just stood, but essentially, you are starting from scratch. while the abled people are up the beach a few metres and their sand is perfectly wet and perfectly dry and the waves never reach it.
then those same people, tell you to just keep building. “eventually you’ll get there!” “keep trying!” “habits take time!” they say. but how? there will always be another wave.
understanding this difference in experience is so important if you want to understand why you can’t just tell a disabled person to form habits or be consistent and expect results.
oh fuck yes.
kind of deeply obsessed with the idea of everyone thinking helia is kind of a dick. like not riven-levels of asshole but most people find him off-putting and hard to get along with by virtue of him being such an intense person. and he’s the kind of person who does things to the beat of his own drum. he’s very one track minded in that way and it makes it hard for others to collaborate with him and find him agreeable on a surface-level capacity. even still people find him likable but in a more distant, unattainable way. but anyone who spends time with him one-on-one and has a conversation with him realizes that he’s actually super non-judgmental and easy to talk to. and he really does like connecting with people, he just doesn’t go out of his way to spend his time on things that don’t catch his attention. and he’s honestly just super sweet.
in contrast, flora is affable and beloved and on average treats people so kindly and sweetly. so everyone’s impression of flora is that she’s a gentle and sweet person who rarely has a bad thing to say about anyone. and while this is partially true, she oftentimes has her private reservations about people that she only truly feels comfortable voicing with her close friends (ie the winx) but won't ever hide from anyone if directly confronted. her natural sociability makes it so that she's very easy to get along with and collaborate with, but people often underestimate her sharp judgment of character and tend to reduce her to her gentleness when she's much more strong-willed than she comes across.
& when helia and flora get together, it's the coupling of two people who are more understated on the surface but actually quite intense to their core. they match each other's freaks <3
I despise the fact that disabled people can never look happy. Or show any form of joy.
Because the moment we do, suddenly we are 'not disabled enough'. As if our existence is solely meant to be pain and misery.