Bowel issues after anal cancer treatment: Had the interstim procedure?
After anal cancer treatment (radiation and chemo) I am having trouble with my bowels. Going to the bathroom 3-4 times a day. Have had physical therapy (pelvic floor) didn't seem to help. This procedure is an insertion of a wire and a pacemaker kind of devise to help control the muscles near the rectum.
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You got it. I stay close to the bathroom every morning. A gastroenterologist prescribed amitriptyln . Off use. It seemed to help for awhile. but then nothing and my gp said it could cause memory problems. So that's where I am at. My surgeon that followed my treatment (no surgery) referred me to the Cleveland Clinic but I live in the Chicago area. Thanks for the info.
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1 ReactionI’ve had bowel incontinence for years. Had my Interstim put in in January after what we thought was a really successful trial. I’m afraid it hasn’t really helped. I have cycled through many many settings and the only thing I can say is that it has made me even more aware of how little time (seconds) I have to get to the bathroom on time. I am currently on a program where the device is turned off for 23 hours and then comes on once a day - no real difference. The thing that seems to be helping the most is trying to make my bowels VERY regular - frustrating problem to be sure.
Providers are kind, but they always say the same things “don’t give up” “everyone is different” “we have other programs to try” . . .
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3 Reactions@currimom
I am having the same experience. I had a successful trial (peeing about every 3 hrs is good enough!) mid-October and have tried 5? 6? Programs since then. I have peed every hour day & night, thrown up, had diarrhea — miserable. Then I end up retaining, having to be catheterized, get a UTI, and have 10 days of antibiotics before we can try a new program. Medtronic rep told me retention patients may take a year to find the solution. I, too, am very overwhelmed and discouraged. Hard to understand how the trial could be so good and the real thing so problematic. I would love to hear from anyone who struggled but did eventually get it right.
I am also interested in hyperbaric oxygen treatment (in addition).
I wish the best of luck to all of you. However, the Medtronic interstim nerve stimulator for bowel incontinince is the biggest mistake I think I’ve made. So after dealing with bowel incontinence for over 10 years, all I can say is that I was more than excited to hear about this device!
I feel like I’ve been scammed. The doctor, the rep, and even Medtronic hasn’t been helpful at all. I’m seriously thinking of removal, but NOW I’m afraid. I can only blame myself, but I will tell anyone who is considering it, please think and research, think and research, think and research.
I had the interstim procedure but it did not work for me. Removal was easy. I still have problems, sometimes I will take an antidiarrheal in the morning and a citracal in the evening. Sometimes it works.
I’ve also has the interstim implanted. I don’t think it is the answer, that it was supposed to be. Possibly it helps a little. I wouldn’t recommend it, but also see no reason to have it removed. My only other option is a total colectomy with apr surgery. No thank you.