guys n girlies,
for many years before my UC was diagnosed i suffered, literaly, with recurring mouth ulcers. A lot of the time they made eating a painfull trauma. Again GP's never offered much help, advice or possible triggers. Stress was a trigger yes but before my colon was removed stress was an issue for me generaly.
Since my Jpouch surgery and my Colon being removed ive not had a SINGLE mouth ulcer! Which one caused what i wonder? if atall. Are mouth ulcers a common thing in people with UC?
But my question and problem is this, very recently i have been getting very small tounge ulcers, nothing like i remember mouth ulcers to be and they only go to my tounge and not my gums as mouth ulcers did. Is it a sign of an issue with my jpouch? I dont suffer with stress since i had my Colon removed, simple as that. My health in many ways improved overnight when they took that outa me. Im sure its not a stress issue infact.
You guys have answered so many questions i had about my condition that so far no health professional has been able too. Im so gratefull.