hot take apparently but just because youre disabled doesnt mean you arent ableist. being disabled doesnt erase your internalized (or externalized) ableism.
if youre paralyzed and you think ambulatory wheelchair users are 'less deserving' of a wheelchair, thats ableism.
if you have adhd and you make fun of autistic people, thats ableism.
if you have dyslexia and think dyscalculia and dyspraxia arent "real problems," thats ableism.
if you have any disability and think ableists should be 'punished' for their ableism by becoming disabled themselves. believe it or not that is in fact ableism, because it perpetuates the idea that disability is something shameful or something that only happens to bad people
gave up on home care and went to hospital on day 15 😭
on day 5 of a migraine get me out of here
Looking more like a checklist these days. I want off this ride. 😭
I prefer Musa in red Enchantix
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.
STUNNING CRIES
Bloom
I’m practicing painting and I’ve been in a winx funk lately
I know I'm shouting into the void with this one but like. Genuinely so many low support needs people dont understand what it's like having even medium support needs. Like I am entirely dependent on other people for many of my needs. I can not see a doctor without someone else scheduling the appointment, taking me there and doing a large amount of the communication for me.
If my caretaker had not been accepting of me being trans and invested hundreds of hours into psych appointments and taking me to my endocrinologist and doing all the paperwork involved with my name change and literally taking a week off work to stay with me in the hospital for surgery etc i would have just like. Never transitioned. My ability to transition was entirely dependent on a singular person and that's what a lot of other parts of my life are like as well. and that's fucking terrifying and a great way to be neglected and abused in ways that are horribly hard to get away from.
I dont drive, I dont work, I struggle to leave the house at all, I dont fucking communicate with people majority of the time. The things that are hard for you? I probably can not do them to begin with. No one in my family lives even close to a comparable life to me. None of my irl friends do. I'm incredibly isolated.
And then I go online and see people rant about how easy MSN and HSN people have it because we just get everything we need and how because people can tell we are disabled everything is so easy because none of you even manage to listen to us talk about the neglect and abuse and trauma we face/d. I see people angry at their (more) disabled siblings for getting care they need to survive instead of mad at society for creating a system where its incredibly hard for families to take care of both a higher support needs child and another child.
And I see people who live completely independent lives who work and drive and make their own doctors appointments and grocery shop and travel by themselves call themselves MSN (I could go on a rant about how that's also often the fault of LSN influencers for not leaving a lot of room in their own community for legitimate struggle but that's for another day).
I just want my needs met. I want to be able to decide where I live. I want choice in my care. I want to be able to have community with those like me. I want others to realize I exist and leave the words i have to describe my existence alone. I want others to listen to what I have to say about what my life is like.
i am so sorry. the being labeled “non compliant,” i understand that so much. they dont see us fighting for our health every day. they only see us for a short appointment or hospital stay and think they can judge us based on that.
im so very glad you have that nurse. 💕
“consistency is key” doesn’t apply to many disabled people.
going to the doctor and having them tell me that, and that i need to stick to a schedule they have deemed appropriate is completely comedic.
what about the fact that my health and ability to do anything is a constant gamble? it can change drastically and almost instantly at any given time.
what about how right now i can stand up and make myself breakfast, but by lunch time? who knows. i may be unable to even sit up.
how do u listen to me explain that i dont have a daily or weekly schedule because of how unpredictable my health is, and reply by giving me a schedule.
do you not think i have tried to stick to a routine and schedule like all the healthy people around me??
all i see is people with consistency. i grew up thinking i was broken because i couldnt. i have pushed myself to breaking points trying to fit your mould of success and health.
im sorry if you experience this too. im going to make another post about what consistency can look like for me and other disabled people. because while we dont fit the classic definition of it, there are ways we can make our own version. i wish doctors would listen to me and would help me find my version instead of insisting on theirs, but they havent, so i wanna try help others find theirs. prt. 2 here (now going to make multiple more posts on this topic lol)