Hey just want to know people in a similar situation
Myalgic encephalomyelitis/ Chronic fatigue syndrome (ME/CFS)
Me too! How long have you been struggling?
I’ve been sick for 5 years (I’m 25 now) got diagnosed in 2020 with fibro but I continue to get worse and worse so finally I got the diagnosis of ME/CFS, POTS and hEDS. Now I’m a severe ME case. And you?
I'm still in the process of being diagnosed. Mines been a gradual case. They first diagnosed me with FND but I've been getting worse and what doctors told me would make it better has made me worse. I'm confident it's ME. I flare between moderate and severe. I'm 27.
Have you found anything that helps? I just got on gabapentin a week or so ago and it's helped with the overall constant pain throughout my body
I don’t have CFS but I’ve got chronic fatigue from another disorder of mine.
33 years old and have a had all of the above for well over a decade now. Then over the last couple years I suffered a concussion as well as covid which caused me to become much more severe.
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