I saw Dr. Hagen yesterday. We discussed two specific items. The first was the results of the x-rays. Dr. Hagen noted that there was a small amount of narrowing at the junction of the pouch to the small intestine. The junction had narrowed to about 8mm. He was not concerned about this and did not feel that the narrowing had contributed to the two vomiting episodes. He had also expected the junction to narrow a bit at this time.
We also discussed the pain that I have been experiencing lately. His first and foremost thought was that I was going through an adjustment period and concluded that as long as food was moving through the pouch, I was having bowel movements, and passing gas there was nothing to worry about. The pain would eventually subside. He told me that should I begin to vomit with every meal, could not have a bowel movement and was in constant pain to come and see him immediately.
His second thought was that the pain could possible be attributed to the bowel being twisted during the original surgery. He felt that this was highly unlikely and really did not want to explore this any further at this time because it basically meant undergoing exploratory surgery.
So here I am at home, frustrated almost to tears with the whole situation. I guess I had expected (hoped) that I would have an easier recovery. I kept imagining myself becoming very active; riding my bike, going to the gym, gardening, and eating regular food with no consequences.
Instead, I constantly remind myself that things could be a lot worse. It has only been 7 weeks since the surgery and in reality I am doing very well. So maybe I am more tired that I had expected, and maybe I am not eating regular food yet, but I am not in the hospital and I am not dead yet!