Experiences with Ileostomy Revision Surgery?

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livinnandlearnin
Jun 17, 2015 9:03 pm

It's starting to look like I'm going to need a revision of my ileostomy. I had a complete colectomy 5 years ago (and many other surgeries since) and blood flow to my stoma is poor now and causing me pain, not to mention how sick I get when I eat. Can anyone tell me what that surgery is like and what to expect as far as recovery? I just got back to my old job in February, getting off disability, and getting my life back. I just can't handle another major surgery. Any info is appreciated.

Immarsh
Jun 19, 2015 4:19 am

Hi I'm marsha, and although I've not had a revision, I did discuss the possibility of needing one with a reputable surgeon.   My ostomy is more than 50 years old, and is somewhat retracted, especially on the bottom.  The surgeon told me that if it was still working, and not causing pain,  do nothing. 

But your situation is different.   From what I understand, they would disconnect the ostomy from whatever side it's on, and then move it to the other side....I know it's a little tricky to find another place on the abdomen....as it depends on your shape , size and previous surgery.  if the stoma part is damaged ( not getting enough blood) then they would probably remove some intestine and refashion a new stoma.   My ex husband had a revision ( yes we both had the surgery...that's how we met)  but his abdomen was in good shape, and they were able to use the same site.  His stoma was really old fashioned....Very long about 4 inches, and because he had crohns disease, it would often get inflamed and swell up, so he couldn't get the appliance on.  Make a list of questions, and do some research, so you can ask  your surgeon what he will be doing.  These days, stoma therapists sometimes help with the placement, so ask him about that also.

 

Best of luck to you.

 

Marsha

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Justbreathe

MeetAnOstoMate website turned out to be a lifesaver for me. I say this because, for me, this ostomy journey was a devastating event both physically and mentally.
Here, I found folks who understood my feelings even better than my family or friends could. Only a fellow ostomate can understand how you really feel.

Information sharing is key, as well as support and understanding, to ultimately bring more harmony into our ostomy life journey. I found here, virtually no ostomy questions that are not touched upon. Questions which some might feel, may be too trivial to contact a doctor about or even too shy or embarrassed to ask their own doctor about. They are all addressed here.

For me, anonymity was very helpful in seeking answers to each phase of this life changing medical and mental event. Sharing initial trauma feelings, ongoing support and finally acceptance was what I found with my membership here. I am not sure what my mental and physical attitude would be today without having found this site.

Additional benefits included: finding products and ideas to help with daily maintenance, innovative ideas and as a bonus - some great humor.
After all “laughter IS the best medicine”.

I have been a member for 3 years, an ostomate for 4 years - yes, I certainly wish I would have found it immediately after surgery but so very thankful I finally found it when I did as I truly believe it turned my troubled depression and situation into a more positive attitude and acceptance.

Sincerely,
An Ileostomate nicknamed Justbreathe 🫶🏼