I am wondering what symptoms people have after having J-Pouch surgery for UC that lead to a Crohn's diagnosis? I have had my J-pouch since 2006 with very little problems. Recently I have starting feeling bad, a lot! I stay exhausted, sleep any time I am not working. No bleeding but trips to the bathroom, urgency and night time leaks seem to have increased. I have a dull pain/burning feeling in my abdominal area, a loss of appetite on some days. Joint pain, some days my ankles hurt so bad it is hard to stand. I'm unsure if any of this is realated to my IBD or not. Any thoughts????