she/they/any pronouns|| 21 || lesbian || disabled || chronic pain and hypermobility || POTS and LongCovid || autistic and adhd ||

298 posts

Who The FUCK Decided That Insurance Companies Get To Decide Whats Medically Necessary????????

Who the FUCK decided that insurance companies get to decide what’s medically necessary????????

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More Posts from Consider-your-potatoes-mashed

Okay, so I love sitting cross legged and it’s the most comfortable position for my body to be in except for the fact that it always makes my left leg fall asleep to the point that it’s extremely painful so I have to keep my leg out straight but that’s not comfortable and hurts other parts of me.

Does this happen to anyone else?


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If someone loves you they will care about how your body feels. Living with chronic pain is tough, and it permeates every inch of our lives. I’m not saying the people around you have to be perfect but they should care about how their decisions can negatively affect you. Expecting you to go to events that hurt you, saying you complain too much, being entirely thoughtless in regards to how your body functions, it isn’t okay. So let’s all stop pretending it is. 

Pnf’s best character arc was buford going from ‘generic bully’ to ‘choatic weirdo’

One of the most annoying things about POTS- I have a separate air conditioning unit from the rest of the house in order to keep my bedroom at the same temperature throughout the day. It's set to 80F° and has not changed at all, but I keep having to bury myself under my thick fluffy blanket and heavy bed comforter because I'm freezing- then I through it off because it's way to hot and I feel like I'm burning up- which sucks. It's like having a fever, but I very much do not have one- I checked .

To summarize my rant about the annoyances of having no body temperature regulation due to POTS- is

Temperature- no change

Body heat- burning up or freezing, switching at random

This is bs- I want a refund on my very dysfunctional body