#and we've just been writing all this into my sister's affidavit so it's very front of mind again
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I'm really, really sorry that happened to your friend, anon. I hope they were able to recover and get justice for what happened to them, and that you've been able to work through it too.
Thank you :) I'm not close enough with her to necessarily be privy to all her deepest feelings, but as far as I can tell, she really is fine and has been for a long time. She's a teacher and doing really well.
And yeah, I don't feel that way--like I'm looking through that filter--anymore, and a big part of that (not to overshare, but hey, maybe someone will read this and it will help them?) was getting diagnosed with generalized anxiety disorder. Since I was a kid I'd felt like violence and death were always lurking, to a degree that was illogical, and then the attack on my friend made that worse because it seemed like oh, I was right to feel that way. But getting worse eventually led to a diagnosis, which has led to getting a lot better! :)
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I'm really glad both you and your friend are doing better and that the diagnosis helped, anon! It's wonderful when diagnoses give us not just a vocabulary and tools for what we experience, but an understanding of ourselves and I guess, context?
Not the same exactly, but my littlest nephew has a severe speech disability which has gone through about five almost-diagnoses and multiple tests which is crazy given he's only 6-years-old. He finally got an actual diagnosis a few months ago (childhood apraxia of speech, or CAS) and while there's complicated feelings involved in knowing talking isn't going to be something that'll ever be easy for him, even just getting to understand it better as a motor disability as opposed to a cognitive one has been extremely useful in helping us to support him in using his voice.
He doesn't really understand what his diagnosis means yet (although he knows people outside of the family struggle to understand him) but it's helped get him into more specific speech therapy and, if my sister wins relocation in family court next month, there's some social groups here in Melbourne where he can hopefully be around kids who are experiencing the same disability (it's a rare one, and there ae just more kids with it in the city) and understand what he's going through as he grows up. So yeah! It's pretty cool when a diagnosis offers not just pathways forwards, but a deeper understanding of self and points of connection too.
#they thought he had cerebral palsy for about 18 months when he was a toddler which was a lot#because the muscular development in his legs was also abnormal#and they needed him to do all these medical tests but then delayed everything because this was at the start of covid and#the doctors were like if he DOES have cerebral palsy he can't be anywhere near a hospital full of sick people during a pandemic#so there's been so many holding patterns#but they had him start seeing a physio for his legs and that basically improved his development#and then they finally did all the cp tests and it wasn't that so it was like two years of weight y'know?#he was born really prematurely and was in nicu for 12 weeks#and we've just been writing all this into my sister's affidavit so it's very front of mind again#but the first two years of his life were just failed development test after failed development test which is just such a shit way#of articulating like#how an infant is growing?#one of my best friend's is actually a nicu nurse and she's always saying we need to change the language around children born prematurely#because they're never going to have normal development milestones in the first two years#but anyway this is way more information than you require hahaha#like i said just front of mind again#anyway his speech therapist now has him practicing pokemon names constantly#and as i often help out with his homework over facetime i now know more pokemon than any adult should haha
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