7·
10 hours agoi wish ill on cis people
0x2640 [pup/pup's, she/her]
silly lil pup
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Joined 1 year ago
Cake day: July 23rd, 2024
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depending on how bent they are they can be repaired somewhat easily
and depending on the pins they might not be necessary for the cpu to run
And then they get in their cars and drive
something something car dependency bad
si, potentially graphic description
the feminine urge to slit my throat and watch the blood run down my body and into the cracks on the floor as the life fades from my eyes and drains from my skin
i better be buried in a dress
6·10 days agoit was welcome advice, promise
ditto on getting a sharps container, very important
leakage does not mean you wasted your dose, it does not mean you “barely got any in”. pain does not mean you “fucked up the injection”. leakage is normal, it wont cause any issues or any levels changes, and it looks like its a lot more than it actually is. pain is just pain, it happens, injecting be like that. same with bleeding, itll happen sometimes, doesnt mean you messed up in any way.
we switched from IM to SQ and had leakage start happening, blood testing showed the exact same levels. many such cases. it really doesnt matter
yea my mum has ME/CFS, no thankies x3 currently looking into a possible *EDS diagnosis, but theres sooo many EDS variations
im aware of most of this (and put a fair amount of it into practice), but thank you!!! just wanted to complain about the medical system from the viewpoint of “i know this isnt what should be happening”
aaaa pocket mirror is so gooddd yes pocket mirror mentioned yippee
speaking from experience: both
so tired of hearing the “not all men are bad” argument for the 129841272nd time
obligatory dont inject hrt intravenously
spoiler
needlephobia issue or? it might take a bit of pressure but… should have no issue going through skin.
spoiler
what do u mean by “didnt inject it right”?
i fucking hate the american medical system
might edit this and go on a rant, might not
edit: rant
so after getting our recent POTS diagnosis they… gave us physical therapy? not sure how exercise is going to help any of the symptoms of pots, or our worsening pain and fatigue, but okay.
we go and realize that this is just… something to condition and gaslight disabled people into thinking that yoga, exercising, and breathing exercises are gonna magically fix their chronic illness. they specifically encourage you to not take breaks and maintain doing all this stuff every single day to and specifically encouraging them to not take breaks and to maintain the same constant activity level to “recondition your autonomic nervous system”, which is definitely how that works. not taking breaks never hurt anybody ever, nope. oh yeah and if you start having symptoms make sure to do these breathing exercises thatll totally do something.
this just seems like a ploy to make disabled people blame themselves for not magically being better, because constantly exercising every single day will totally make me less disabled. “oh its not working? well thats your fault! try harder”. cant wait for them to start saying “theres nothing we can do and we are going to forcibly euthanize you”.
forgot to add that i have another unknown chronic illness, and depending on what it is doing literally any of this could be completely terrible for me.
oh and when our lung collapsed last year they literally told us to “walk it off” and that “it would heal on its own”. (it didnt, we had to have major surgery)
down with cis
up with trans
our cat destroyed our headphone cable and we had to pay obscene next day shipping costs because we cant exist without our headphones
*dies*