A.C.E. stands for "Antegrade Colonic Enema." An A.C.E. procedure allows the patient to do a total washout of their colon by flushing out stool starting in the colon downward. This produces a bowel movement under the patient's control!
A very small opening (ostomy) is made in the patient's belly button or lower tummy. This opening can be made so small that it is barely visible. The ostomy is used to flush a saline solution into the patient's colon to wash it out and produce a bowel movement. This may be done daily, every other day, or 2-3 times a week, depending on how often cleansing is needed. Staying on a good schedule will help keep the patient's underclothes clean in between flushes. This ostomy is called a "continent ostomy," which means that fluids only go into the opening. It is not made for stool to come out of.
They turned my ileo into an A.C.E, which is better no doubt as I have more control. My bowel extracts a lot more water than normal ones, so by the time my stool is at the bottom it can be very hard and wide and painful to pass even though I do keep well hydrated. So putting in some solution once or twice a week keeps things soft. But sometimes gas and fluids do come out at the stoma end, and because I only wear a stoma cap, there isn't much room if it does.
I was wondering if anyone has an A.C.E on here and uses a stopper or has any other tips.
Regards