Hi everyone! I just had my first scope last week. The reason it took so long for me to get it done was because my original doctor kept telling me to wait until my flare was over to do it, then he just dropped off the face of the earth and I had to find a new doctor. Luckily my GP prescribed me steroids in the mean time, I take a small dose, 5mg, but without it I'm in so much pain I can't function or go to work. I woke up from my scope screaming and crying and overwhelmed with anxiety. I don't know why. They told me my intestines were so narrow they had to use a pediatric hose and could barely navigate that through. They found several large polyps at my cecum. I don't know why he didn't remove them. They were the type that are imbedded in the intestine. Everything I've been reading since then and all my symptoms are pointing to cancer, even though several doctors have told me I have crohns. Now I'm anxiously waiting the results of my biopsy. The doctor said he would call me, but I haven't heard anything yet. I'm in so much fear and stress that it might be cancer. Has anyone else had a lot of polyps in the cecum? Has anyone had them develop into cancer?