Anyone else have this? I have not been officially dx but I am sure this is what I have. For some reason it is becoming increasingly more symptomatic bordering on chronic.
Hard to say whether to blame this on Lyme. I tend to only because Lyme has made my joints and connective tissues very loose.
I eat properly but even drinking too much water can set it off.
Posted by Lymetoo (Member # 743) on :
Have you been checked for EDS and Mast Cell Activation Syndrome?
EDS involves connective tissues and joints .. MCAS would affect the gut. Many of us have acid reflux from it.