Posted 8/21/2016 10:02 PM (GMT -5)
Thank you for your replies.
Bloom93, thank you for the information about calprotectin. The GI seems to put a huge amount of emphasis on the calprotectin results, given that my son has very few symptoms, his ESR and CRP are normal but he said apparently these tests are less accurate. I guess I worry about the impact of ongoing inflammation.
DBwithUC thank you for that information. I guess I wonder about UC as his symptoms don't seem typical, not having bowel motions more than once a day, he was so young for the uc diagnosis I thought allergies might be more likely, only ever having blood one day, which may not have been uc related, that fact that he started a gluten free diet at the same time as the medication or maybe i'm just in denial and desperately hoping it's not uc.
His original colonoscopy showed crypt distortion and crypitis, I wonder if this could be caused by something other than uc like a food intolerance. Given that gluten caused his coeliac damage I thought another intolerance may have cause the lower bowel damage.
Although I want to try him off mesalazine I am also scared to, the GI said he may get worse and then the mesalazine may no longer work if we put him back on it and would have to move up to drugs with more side effects, but I also wonder if for example he had a sacylite allergy mesalazine could be making things worse.