Thanks for keeping us updated on your progress post remicade. 6 mos with no flare is wonderful. I am now temporarily off remi (skipped the Dec 5 dose) to see how things progresss and off 6mp due to the increasingly elevated liver enzymes and positive autoimmune hepatitis markers. It was the rhematologist who suggested the skip in remi and a hepatologist who ordered me to cut back, and then off 6mp. They are both mature experienced doctors who I greatly respect.
I don't know if you saw the earlier posts about how studies showed you could go back on the biologics like remicade, if necessary, and it will work. Based on that, and your experience, I am pretty sure I will not go back to the remicade or entyvio or anything, unless and until I have a flare. I want to give it as much time as possible to see if the pain goes away, and give my liver time to hopefully heal.
I have found the posts of you and Thoreau and those of several others regarding remi, pain, 6mp and a few other topics to be especially helpful to me in my journey through this terrible disease, the medication side effects, the bewildering medical profession. I think I now have a game plan for the future.