Dysautonomia

Hey, I’m Katie and new here. 😊 I’m 26 and have ME/CFS, fibromyalgia, endometriosis, Sjögren’s, dysautonomia, and HEDS. My biggest struggle is by far my chronic fatigue syndrome, which I’ve been dealing with for the past 10 years. Would love to meet other people on here that can relate to any of the aforementioned. 💗

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Just had to drop out of college because of the severity of my POTS and Dysautonomia..... I’m doing anything to keep me from spiraling. Any suggestions on good practices for staying in good mental health?

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I have Dysautonomia and POTS and I’ve been taking thermotabs (salt tablets) daily for fatigue. It also helps avoid dizziness while standing/walking. Due to the virus, I’m unable to get salt tablets. Any other suggestions?

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Does anyone have information on dysautonomia? My neurologist mentioned it, but isn’t super familiar; and my rheumatologist just tried to send me back to him about it...

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Hey guys! I’m new here and I’m just really looking for support and understanding. I was diagnosed with POTS and Dysautonomia almost a year ago. I just feel so alone and such a burden since I’m always sick. I feel like no ones fighting for me besides me. Any advice?

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anyone else here with dysautonomia and/or MS? I also have hashimotos and raynauds. #blessed ;)

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