I was hoping to hear from others on their experience of their IBD with an ileostomy. I find it hard to know whether my Crohns is active given the ostomy. I dont have the pain or discomfort etc I used to have and I also kind of just push through any tiredness etc or mouth ulcers etc I might have. Having worked my way through Humira, Infliximab, Entiviyo and now on Stelara I cant tell if any of these actually worked or not. Normal bloods, CRP etc fairly normal. What are your experiences please?