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#low blood pressure feels like the room is spinning and im unsteady on my feet and i get so nauseous
salt-baby · 2 years
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one of the really fascinating things about chronic illness and ableist doctors is how little they trust me to distinguish things about my body
I think for them it's very easy to say 'okay pain caused by nerves is a dull diffuse pain and pain caused by joint dislocation is also a dull diffuse pain so I need to do further testing to distinguish them'
but for patients who live with it it's very easy to distinguish the two! in fact with as much time as I spend with it I'm very good at telling what my body's symptoms mean! they're important warning lights for managing my condition!
nerve pain feels different than joint injury pain and they respond to very different treatment! it's extremely beneficial for me to learn the difference so of course I have!
it's just so frustrating for my doctors to go "oh your wrists hurt? let's do a nerve assessment" and for me to say "I don't tend to get nerve pain in my hands and that's not the pain I want addressed" and then have the doc go "ehhhhhhhhh let's run the test"
i feel like I'm constantly having my personal experience on this dismissed, on everything from distinguishing low blood sugar and low blood pressure to differentiating the types of fatigue and sleepiness I experience
disabled people tend to know their own bodies best, and the bulk of management of their conditions will be done by them alone, and I just really wish doctors would listen to them a little more.
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