Posted 3/14/2012 9:55 PM (GMT 0)
Hi,
Most of you know my story, what turned out being an unneeded sigmoid resection for what I was told was pelvic organ prolapse symptoms of divided bowel moves, lead me to severe scarring and loss of colon, rectum, and small bowel. Then lucky enough to find a surgeon who got the scar tissue off my small bowel and did the ileostomy for me thus saving my life.
Well, he retired, my replacement surgeon is now writing up very odd records saying I have/had a disease etc, etc.
After my last food blockage on tuna this weekend, I asked that he call. He did last night and he said basically that my intestines never worked right and I was searching for a mechanical solution to a functional issue. I said back when I had the original sigmoid resection I was told by three colorectal surgeons at other hospitals that my sigmoid colon was blocking off my rectum (sigmoidocele). I obviously did not know at the time that it was not or I obviously would not have had it out. None of those original docs did funcntional studies.
So I reminded this doc that I needed the ileostomy and take down of small bowel adhesions due to scarring of colon, rectum, small bowel from that first surgery. I did not hammer on about the details. BUT get this, he flat out said words to the effect, scar tissue can't change the function of intestines that much.
YES it can. I had small bowel obstructions for a year due to scar tissue on my small bowel. ONce it was removed, so far no adhesion reobstruction, just these stomal level food obstructions.
What the heck to you all make of this? Surgeons know about adhesions they lyse them every day. He said he did not know why I was developing small bowel dysfunction. I don't have that. It functions fine. Transit is three hours totally normal. The issue is at the stoma. Something is going wrong at the stoma level where poop gets trapped. What is his agenda. I am getting scared. He says no tests, no meds, nothing to do, it's your dysfunction. Sounds like a wimp out to me.
Rosemary