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Myalgic Encephalomyelitis Community

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All posts for March 2023

Covid 19 has it worsen your ME/CFS symptoms?

Good morning all! I was wondering if any of you caught Covid 19 that made their ...
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theia
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Long-term experiences of managing Chronic Fatigue Syndrome/ Myalgic Encephalomyelitis (CFS/ME): A qualitative study

Another useful doctoral study:. Williams, D. S. (2016). Long-term experiences ...
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A life lived differently: an exploration of how living with CFS/ME impacts upon people's identity

I just came across this important doctoral research and thought to share it w...
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2 Replies
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Do anybody get seizures or type of movement disorder from me/cfs?

Just wondering as I'm not diagnosed with cfs but my symptoms point to it.I've be...
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Charts
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