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It would explain why it feels like my body is literally wanting to shut down
I don’t have confirmed ME/CFS yet, my functional med clinic wrote CFS as a diagnosis in my chart but I don’t know how official that is. Been dx with POTS and possible Dysautonomia. What I do know is that since Feb I have severe post exertional malaise and I’ve housebound, now this month I have been bed bound.That seems alarming. I know very little about this but I wonder if everyone with cfs/me would have similar, or just elevated, results?
Thank you for that link. Definitely have lots of GI issues and sounds like a possible cause.You might be interested in this thread as well: https://forums.phoenixrising.me/thr...dosis-as-cause-of-symptoms-and-illness.57613/
And I agree with Artemisia. If you have PEM, you likely have ME/CFS because it seems very specific to our disease.
You could also check your symptoms against the CCC: https://me-pedia.org/wiki/Canadian_Consensus_Criteria
After reading that thread my mutation would explain everything. MYLK codes for Myosin Light Chain Kinase which is crucial to the contraction of smooth muscle cells>gastric dysmotility>SIBO>D-Lactic Acidosis and would also explain PEM except through a different mechanism(dysfunctional vaso regulation)You might be interested in this thread as well: https://forums.phoenixrising.me/thr...dosis-as-cause-of-symptoms-and-illness.57613/
And I agree with Artemisia. If you have PEM, you likely have ME/CFS because it seems very specific to our disease.
You could also check your symptoms against the CCC: https://me-pedia.org/wiki/Canadian_Consensus_Criteria