12 days agoIve got all except shaky in the heat and fainting but I know I dont have POTS the hell is wrong with me😭😭
2 months agoPOTS is SO MUCH MORE COMPLEX than people give it credit for!!!! especially alongside things like MCAS🥲🥲
2 months agoOmg i didnt know raynauds is pots related . Ive got that too. Thanks girl...and keep hangin on. ❤️❤️
3 months agoMy dr said I can't have raynaud's bc I have POTS 🙃 I have a family history of it too
3 months agoMine were the same one gone to the ER so many times from being overheated and almost passing out
3 months agoOne of my weird symptoms (im not diagnosed but i have all the symptoms and a common comorbidity; EDS) is itchy legs. Ive only seen ONE other person mention this symptom. It only affects me when i stand still for too long (so not a rash) and is accompanied by my legs and a scar on my wrist turning purple, aka blood pooling. My dysautonomia seems to be worsening as of late as I've fallen twice after getting up (like my head would go blank and my body like jelly, but not fully fainting as i maintained consciousness and got better once i hit the ground) and flopped onto the ground before i fully fell one other time in the span of a week.
3 months agoRashes and swelling also can be MCAS which is HUGELY co-occurring in those of us with POTS.
3 months ago🙃🙃 I had a heart Dr tell me Pots isn't real and "tossed around a lot". This is literally every issue I've been dealing with and the ultimate diagnosis from Drs was "idk bestie, cope."
