Has anyone been told they have leaky bowel? My new GI doc said I have leaky bowel and probably have had it for some time. I am taking EnteraGam for it and have been on it for months now with no noticeable change in my symptoms. He said the EnteraGam helps to heal the cells of the bowel wall and stop toxins from entering the bloodstream. I have an appt with him this afternoon and will ask him what is a reasonable amount of time before I might see some improvement. I am feeling quite discouraged in general as it has now been one full year since my colon was removed (Aug 2014) and approaching my take down anniversary in November. It seemed like that one year mark was the goal for reaching some degree of normalcy, albeit it would be a new normal, and I have in my opinion gotten worse. I know my diseased colon is gone but from a functional point of view, I am worse off. I have pain after eating everything, there are very few times I eat something that I do not bloat and need a bathroom pretty quickly. Sometimes it is worse than others. I feel like I have had every test imaginable--although I am sure there are more forms of torture out there, and there doesn't seem to be an explanation for why my body is just not adjusting to having this J-pouch!! I know there are others of you out there that have felt this frustration. I have been scoped and my surgeon says no pouchitis. But I am on Flagyl and that has reduced the number of bowel movements and helped with the diarrhea. I am sure of that as this new GI doc took me off the Flagyl and within about 6-7 days the diarrhea was back with a vengeance. So back on the Flagyl, also take a probiotic and the Enteragam. Also unfortunately about 3 weeks ago had to have a PICC line put in for TPN because of weight loss and malnutrition. I am small, only 5'2" but had dropped to 83 pounds and it was headed in the wrong direction so as much as I hate it the TPN has started to put some pounds on me. I had TPN before so I know it does work but this time it has not gone smoothly, was infused too quickly at first and had a terrible blood sugar reaction and felt nausea and woozy within an hour or so of starting the infusion. Fortunately the dietician from the pharmacy figured it out from my symptoms. The doc wanted to give me some freedom and just do the TPN for 12 hours, overnight, 7-7 or whatever but that was too much too fast at my weight and she had to re-calculate the rate and so I am stuck with this TPN bag for 22 hours a day. I still don't feel good for some reason this time. I am gaining weight but don't have any energy or strength. I expected as the weight came on, I would start to feel a lot better. One more thing to be frustrated about!! I doubt the doc will have an answer about that as it seems they know little about TPN as I have learned. I will speak to the dietician again as she is wonderful, very caring and knowledge. But none of that is solving the problem of why I can't eat normally and digest foods without bloating, pain and bathroom problems. I knew I would have frequent bowel movements, I was not unrealistic, but I am still in so much pain!! I had to very difficult surgeries, 12 days in the hospital for both, we all know the complications we all endured might be different but let's face it, none of us would be on this message board if we were amongst those that had a text book experience and went on with their lives happily ever after!! My life has been at a standstill for years and had so much hope that I finally had the answer. Now I feel like I don't even know what to hope for. Is it likely that my body will just suddenly start functioning like it is supposed to?? I know some people on here have done a diversion to give things a rest, others have just ditched this pouch and gone back to the colostomy bag. How do you know when it is time to call it quits on this? Should I be setting some type of deadline and after that, move on with Plan B? I know there is never a good time but....we will be moving (locally) soon and my daughter is having a baby in January. Our first grandchild!! Another reason to want to feel good and be healthy and not need someone to take care of me!! I don't live in a huge metropolitan area and have already seen 2 GI docs in one big group and am now seeing a GI doc in another. I have been to Vanderbilt's GI group. Didn't care for the doc I saw there although she was probably brilliant. How hard is it to get into some of these Drs at Cleveland Clinic many of you have mentioned? Part of me thinks I am not there yet, I mean there must be more that can be done here but it is exhausting as you well know. Any and all advice would be appreciated. Heading to dr. appointment shortly.
Thanks for listening.