Hello. I am scheduled to have this surgery soon to remove my rectum. I already have an ileostomy because of ulcerative colitis so I don't have to worry about that. And I've read many of the posts of the surgery and recovery. But I wanted to actually ask for myself about the recovery and get some advice. I'm scheduled to have it May 22nd so it's coming up. I actually would not have known how bad my rectum is had I not got an obstruction and was told by my surgeon, who did my other surgeries and will be doing this surgery, I should get my rectum checked out. With the sigmoidoscopy they could only check about one inch of my 6-7 inch rectum cause it was so inflamed. Doesn't bother me at all I hardly know it's there but it is a threat to me and I have no choice but to get it removed since they can't check it for cancer. I will have 6 weeks off work at least to recover. I work a very physical job doing janitorial with a plan to become a Facilities Maintenance Engineer/Specialist, which is a very physical job as well. I like to be active and I walk a lot. I walk my dogs often and chase them in the field. I like to ride my bike. I'm pretty healthy right now and in good shape and am actually preparing for this. Much different than when I was sick and in the hospital for 4 weeks before they removed my colon and I was there another 2 weeks. 6 weeks total. I know there's a lot of stuff I won't be able to do for some time. And I know I'm gonna need to make adjustments to my life. So any advice is appreciated like how your recovery was, like length of time, difficulties, pain, adjustments, and what your abilities are now. Also if anyone had any complications. My surgeon is very good and I trust him, but I know with this surgery it can be done to 100% success with no errors and there could still be complications. I feel alright about the surgery. I'd rather not have to have this done, but it is well with my soul, and I think this will help prepare me even more. So anyway thank you to anyone who responds to this post and God bless you.
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About seven years ago, just about every aspect of my life was ostomy related. From the moment I was told an ostomy might be needed until some months down the road I existed as a person afflicted with a colostomy. I feared someone other than my immediate family might find out I had a bag. Ugh! What could be worse? Suppose it filled real fast when I was out with no place to hide and take care of myself. God forbid should it leak in church! Suppose I roll over on it in bed. I was a lesser creature, destined to a life of emotional anguish and physical routines different from most of the rest of the world. I felt like a freak. Then I found folks like you guys here, read your stuff, really “listened” to what you had to say and I began looking at things differently. We know perception is everything and I began to understand how good things were relative to what they could’ve been. So many folks had it so much worse than I did. That didn’t make my discomfort go away but it exposed how fortunate I was to be dealing with my stuff and not their’s. I felt a little guilt, maybe selfishness but quickly forgave myself by understanding I just wasn’t smart enough to fix my feelings. Then, I wonder what smarts have to do with feelings. My perception was warped so my perspective toward my existence was warped.
I learned over the last few years with the help of lots of folks right here at MAO that I could be better at living just by accepting some facts. It is what it is and so what? It’s not the worst thing to happen to a person.
I think everything is, in some way, related to everything else. I just put the ostomy thing in the back seat and drive forward.
Respectfully,
Mike
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