#my neurologist said it probably triggered cfs/me and that its basically a form a long covid
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The thing about chronic pain is that I'll be experiencing the usual horrors (pain and discomfort that isn't possible to fully ignore) but I'm not even phased, like this is just a normal Wednesday night for me.
#it hurts but i can ignore it if i keep myself occupied with other stuff#which means its not that bad#but its bad enough that trying to sleep is out of the question#and that means its another night of taking melatonin with as much advil as my kidneys can tolerate and hoping for the best#disabilty pride month except instead of pride i feel nothing but apathy and discomfort#ngl i am getting more and more discouraged as time goes on bc i am getting less and less good days#and i am losing abilities ive always taken for granted#like being able to drive for longer than 20 minutes#or doing chores#or literally just being able to stand long enough to like cook a single without it using up all my energy for the day#not even exaggerating#i can at best cook one meal a day now#on bad days i cannot cook anything that cant just be microwaved or popped in the toaster#ever since i had covid last summer it seems like my health started getting worse at a much faster rate that it was before#my neurologist said it probably triggered cfs/me and that its basically a form a long covid#which fucking sucks so bad#like exercise helps some of my other conditions but i cannot exercise at all anymore without triggering a bad crash#there is no winning#siiiiiiiiiiigh#its fine though#we carry on
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