69constellationsinatrenchcoat - misadventures of a queer disabled DID system
misadventures of a queer disabled DID system

No, there are not 69 of us but we are hiding in a trenchcoat.. medically recognised adult DID system studying to become a clinical psych. We are aware we make mistakes, we know we make mistakes, we're open to kind discussion!!!! 🇳🇿🏳️‍🌈🏳️‍⚧️ Please remember, there is a person behind almost every post on the internet, including syscourse. Be kind.

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I Bet It's Confusing Talking To Me Because I'll Sometimes Refer To Us, As..well, Us But If In Talking

I bet it's confusing talking to me because I'll sometimes refer to us, as..well, us but if in talking about myself I'll use "me/I".

"we're hungry" is a collective experience in the body (even if individual alters feel it differently)

Whereas "I'm bored" is an individual experience, specific to the alter fronting.

But sometimes I'll be talking and I'll say "we did x last week, I remember it really well!" Because...we, the body, did it, but I have individual experience with it.

Plus sometimes I'm so used to saying me/I that I slip up and say the wrong thing 🤣

[This post was directly inspired by @toxicity-2003, thank u]

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More Posts from 69constellationsinatrenchcoat

is it really so foreign for the average person to conceptualize others being chronically ill?

i sat down and was part of a twenty-minute-long, coherent group conversation where i faked being more alert and less brain-foggy than i was. it drained a chunk of energy, but i managed it

then this woman said something along the lines of, “a couple years ago, you had some chronic pain, right? so nice to see you on the other side of that!”

no one said i got better. i hadn’t been able to stand for the majority of the conversation. but i guess i looked recovered? despite me being more limited than ever?

i don’t understand the world these people live in. the pain and fatigue will be with me until i die

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