
32. she/her. disabled. osdd & cptsd. sex trafficking survivor. posts might be triggering.
196 posts
"i Would Kill For You" "i Would Die For You" Okay But Would You Forgive Me If I Forgot Something Important
"i would kill for you" "i would die for you" okay but would you forgive me if i forgot something important for the 51204th time in a row even though i tried my best to remember
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More Posts from Dissociatedbi
“do you really wanna be on medication for the rest of your life” if you knew me unmedicated you’d want me to be on medication for the rest of my life too
Recently I keep thinking about how I wasn't allowed to clean myself properly as a child. My mother was obsessed with ridiculing me for my general hygiene making her look bad, but didn't allow me to condition my hair or moisturize my face or use soap on certain areas of my body. Like why? If you're so obsessed with how I look, why are you trying to make me look bad?
i can get to my desk IF someone moves a chair out of the way is not accessibility
i can get in the building IF i’m having a really good day and can open the door myself is not accessibility
i can get in the building IF i go through loopholes to be allowed to use the accessible entrance is not accessibility
i can get to one desk BUT i don’t have a choice in where i sit and everyone else does is not accessibility
there is an accessible entrance BUT it is farther away and more inconveniently placed than any inaccessible entrance is not accessibility
accessibility should not have conditions. all of these are still good, compared to absolutely no access. but disabled people should not have to settle for “just barely good enough”
people vaguely saying 'the horrors' as shorthand for 'life problems, don't worry about it' in conversations where the problems are not going to be delved into has got to be one of my favorite new Ways Of Speaking that has emerged. like it's polite and vague and succinct enough for impersonal conversation but also extremely honest. it's very funny. The Horrors. we all know of them.
Something I haven't seen spoken about a lot is the psychological impact of being chronically ill and experiencing horrific symptoms, and knowing that literally no one can help you.
I could call a doctor, but I already know what's wrong. There's literally nothing they can do for me. And I can't afford to go just for reassurance.
I'm just in a flare and sometimes it's Like This. And you just have to swallow symptoms that live in the nightmares of well people, because you can't just have an emotional breakdown every time you're in a flare.
So I'm in horrible pain and distress, and I can't call for help, because no one can help me, and I have to act like it's fine, so I don't worry other people who get Very Upset that I can't just Fix It
And there's just a deep psychological burden in that, that I don't think well and able bodied people ever really think about.