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I got my POTS diagnosis 7yrs ago after I passed out and fell down a flight of stairs. I HATE how people assume I just pulled the diagnosis out of my ass recently due to “tiktok trends” when they see me being “visibility disabled” for the first time. 🫩
“POTS is a social media trend” yeah okay buddy tell me that again when i pass tf out and then throw up violently for fifteen minutes after
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Anonymous 13h

its really just very thinly veiled misogyny bc its a disorder in which over 80% of the population are women/afab

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Anonymous replying to -> #1 6h

I once had neuroimmuneologist I waited multiple months and traveled hours to see tell me “We see a lot of women your age with a medical history of anxiety have these issues” and then he refused to run any additional tests and referred me to an online FND clinic. When I told him my other doctor ALREADY RULLED IT OUT- he insinuated that he thinks that “at least 30% of doctors think something is a rare disease when it’s actually FND”- which is a nonsense statistic not backed by any data. 💀💀💀

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