My husband used to have a lot of mucus prior to the illeostomy. He was told to stay away from milk and dairy products and it seemed to help a little bit. His crohns started in his stomach, then moved to the large intestine and that is when they knew it wasn't just a stomach ulcer. His regular doctor wanted him to have surgery right away and that is when he started seeing a GI specialist who told him they would treat it with meds as long as they could. His first surgery was in 1987 for a fistula and we knew that was the just the start of more surgeries and then in 1989 he was so sick that he was in the hospital for a week before they could even do the surgery. Actually his colonoscopy showed his large intestine wasn't that bad and when they
opened him it was so thin and adhered to everything that his surgery took over 7 hours instead of the 3 1/2 they told me. After they removed his large it shifted to his small intestine. After every surgery he tells me he isn't going through it again and I don't blame him. He also lives on tramadol to help with the pain and the fatigue. Our two children (25 and 23) both have intestinal problems but so far they haven't been diagnosed with crohns. He has 3 sisters who have intestinal/stomach problems and he lost his older brother to colon cancer. I also have a niece (my brothers daughter) who was diagnosed 9 years ago with crohns. This is a terrible disease that they still do not know a lot about
. I think you are making the right decision at least from what we have experienced - you know your body better than the doctors. Good luck and try to stay positive. Good Luck.