u/e1ectro-cutie

advice?

22f. so july 4th i was diagnosed with a uti. july 5th i was in the er and diagnosed with a kidney stone (3mm right side) as well as mild kidney swelling (right side)
given flomax for a week, cephalexin for 5 days (500mg 2x daily), and was admitted for 24 hours and given 2 doses of an iv antibiotic.
they initially said i met the criteria for sepsis at that time, but they were toooo sure
i was discharged but went back to the er a few days later. they then found an ovarian cyst on again... the right side (4.9cm x 4.5cm x 4.5cm) they believe that was related to my cycle though. bladder infection was also diagnosed.
i did pass my stone on july 22 and got it confirmed as calcium oxalate (i have issues hydrating and im seeing a doctor about that of course)

however, i have been bedridden and deconditioned from this whole ordeal. struggling to get up without assistance, spending my days in bed. i am doing some recumbent pt for the time being but my main concern is my chronic nausea that has been a thing for longer than all of this. i normally rotate between hydroxyzine, promethazine, and zofran. i have been taking them for months to years (depending on the med) and have had no issues with them at all. however, in the peak of all of this i was haven some cardiac symptoms (that were cleared). heart palpitations, chest pain, dyspnea. again, medically cleared and i have a cardiologist who has done extensive testing. she thinks its ist and costochondritis. my biggest question.... can i start my prn nausea meds again? i can't tell if the palpitations were related or not. it's been about 2 weeks since i've stopped them. i've tried ginger, peppermint, b6, etc but nothing comes close to my rx meds. i don't want to make a stupid mistake and get hurt but i would like an outside opinion as my doctor hasn't really given me any clear answers at all despite me asking a few times. i understand this isn't going to be 100% medical advice, i really just want to have a few outside opinions on this situation so i can come to my doctor with some more information and potential solutions

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u/e1ectro-cutie — 18 hours ago

shower trigger

so my doctor is suspecting costochondritis as my numerous cardio work-ups and extensive tests come back clear. for some background, i have been bedridden for about a month now following a dysautonomia flare from a kidney stone. i have deconditioned from that and today i finally showered. i sat the entire time and had my girlfriend help me do most of the work. hours later the pain is so flared and tight. does this delayed reaction happen to anyone else? colder shower next time? weird because heating pads tremendously help my flares, so why would the shower hurt?

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u/e1ectro-cutie — 1 day ago