• this user has complicated feelings about being physically disabled
Realizing ur a therian is wild like wdym I'm a dog there's no way I could... *reflects on entire life* oh... damn I am
i am BEGGING people to please stop spreading this sentiment without the appropriate nuance. I irreparably damaged my shoulders by using a mobility aid that wasn’t right for me because I was told “just get the cane!”
Mobility aid use is a serious medical decision. Absolutely do NOT get crutches because you “think they would make you look cool.” You have a high chance of causing avoidable, permanent damage to your body.
If you are unable to be seen by an occupational therapist, please make sure to do research on different mobility aids and how to best use them for your needs. It can make a world of difference in your future ability.
to those who want a mobility aide, but don't think they're "disabled enough" for it:
get the aide.
you want a cane, but you don't think you need it? get the cane.
you want a wheelchair, but you can get by without? get the wheelchair.
you think crutches would make you look cool? get the crutches.
it doesn't matter if you just think it looks cool or fun. using mobility aides actively helps those of us who do 100% need them, even if you don't ""need"" them.
using mobility aides in public makes it easier for others to do so. buying mobility aides, especially things like canes, often means that they continue to be made and supplied. sometimes, disabled folks make and supply mobility aides - in that case, you may be directly supporting them.
get the mobility aide. use it. you're doing good.
random musing.
something i really love about life right now is the silent wobble of solidarity when i see another person who has a movement disorder. i wobbled past a guy with cerebral palsy at the store and he raised his T-rex hand to me like it was a gang sign. hell yeah we may be wobbly but we’ll be wobbly together
every day I'm clocking in for my shift at the not making sense factory . we don't know what we're making only that it's not sense.
people who don’t believe in endogenic systems are so fucking arrogant. “I’m the expert of YOUR experience, and I don’t think you’re really experiencing what you say you are.” as if you are the sole true understander of cognition and everyone else is just making it up
it is so ironic that there are people who will take posts made by endogenic systems that are spreading positive messages and repost the exact same post but add ‘endos fuck off’ to the tags.
‘if you tell me youre a system i will believe you, unless youre a gross endogenic system in which case i hate you.’ my brother in christ how do you NOT see the irony.
I think people with brain damage and neurodegenerative diseases' unique position on brain/body duality is so heavily appropriated by others and used to speak over us or put words in our mouths that I don't think we're ever actually allowed to speak about it ourselves. That's a huge loss I think, because I think we really do have a lot to say that could be very beneficial to the community and disability rights as a whole. Even to our understanding of the human experience and its physical nature, I think.
To have your body tangibly damaged, and through it your entire world and self too, to be changed so intrinsically that it spans both the body and the very essence of self. The inseparability of your physical disabilities and who you are not just on a spiritual or social level but a tangible, physical, neurological one, where even in a hypothetical future you couldn't cure the physical without changing the self, everything you experience, in ways that can be almost impossible to comprehend. The absolute, unavoidable understanding of every fiber of one's self as a physical phenomena, down to the very last thought or feeling, and coming to terms with it.
Unfortunately I think unless people stop using us as a mouthpiece to talk over each other, we won't get to have those conversations. If you want us to speak, you need to listen. I mean really listen. No picking and choosing, no deciding for us what you think it means. No trying to relate our experiences to your own when we tell you that no, those things aren't the same. Just listen and uplift our voices, especially those of us who can't communicate our thoughts and experiences very well.
really wish able bodied people would stop infiltrating SCI communities to ask about their back pain. that’s not what a fucking SCI is you two-legged fuckwit
needed this today so im reblogging it in case someone else does too
Sometimes your worst fears are true. Sometimes you’ve annoyed a loved one. Sometimes you’ve even upset them or frustrated them.
But you know what? It doesn’t mean they’re done with you. It doesn’t mean they’re going to leave you.
It is normal to be annoying sometimes. It’s normal to not be perfect and to have off days. It’s normal for relationships to not be in perfect harmony all the time.
My point here is, yes, while sometimes they are true, it isn’t the end of everything. It’s actually quite normal. And you’re going to be okay.
AND I WILL NEVER DIE
I WILL NEVER DIE
I WILL NEVER DIE
I WILL NEVER DIE
I ACCIDENTALLY POSTED THE DRAFT EARLY OH MY GODDD
anyways this is finally done i can rest goodbye
i don’t rlly know what to say other than that,, here’s the textless version and the sketch because i think the sketch is cool and the textless version is lowkey better💔💔
21 yo physically + cognitively disabled dogboy. complicatedly and tentatively plural. disability awareness/advocacy and sometimes kink posts. artist and musician who likes to wax poetic about silly things.
52 posts