Myalgic Encephalomyelitis Community | HealthUnlocked
Myalgic Encephalomyelitis Community
1,310 members • 456 posts
What was your experience at the doctor on diagnosis?
Hi all, I was diagnosed with CFS in 2015 - and still have it. I remember maintaining at the time of diagnosis that my health issues stemmed from a physical...
Hi all, I was diagnosed with CFS in 2015 - and still have it. I remember maintai...
a month ago
My meningitis (andME) was caused by lymes disease
Anybody with bacterial meningitis been tested for lymes disease? Or did you have suspected viral meningitis and nothing was detected for proof? I was the...
Anybody with bacterial meningitis been tested for lymes disease? Or did you have...
19 days ago
Want to be a Community Ambassador for Myalgic Encephalomyelitis Community?
What we are looking for We accept all applications, but ideal candidates are members that have been active in the community for at least 6 months. Why you...
What we are looking for We accept all applications, but ideal candidates are me...
5 days ago
High Serum C. Should I be concerned?
Hi all, I'm new here I found this site while looking for advice on my health. I was diagnosed with CFS/ME 3 years ago but I have never been refered to a...
Hi all, I'm new here I found this site while looking for advice on my health. I ...
17 days ago
My SIBO, CFS, IBS recovery plan
Hello Everyone! My name is David. I have suffered from chronic fatigue for many years. I have recently tested positive for Methan Dominant SIBO. I have started...
Hello Everyone! My name is David. I have suffered from chronic fatigue for many ...
4 days ago
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What characteristics does your ME pain have?
If ever been seen by UK 'CFS/ME' clinics what was your experience? Tick any that apply. (Will be more polls on this subject in future too!)
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