Adult inutssusception
Posted , 4 users are following.
Hello anyone with this condition please make contact.
Any one with a gangrene related intussuception?
How did your symptoms begin?
What procedures did you have?
Make contact.
0 likes, 11 replies
debbie58553 sandra2468
Posted
sandra2468 debbie58553
Posted
New Year Greetings to you.
You said you had just come out of hospital.
Did you havve a suregery?
Best wishes,
Sandra
kathy90352 sandra2468
Posted
ella19927 kathy90352
Posted
kathy90352 ella19927
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ella19927 kathy90352
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kathy90352 ella19927
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kathy90352 sandra2468
Posted
sandra2468 kathy90352
Posted
Sorry for late reply.
Has anyone offered you irrigation.
What did the colorectal surgeon advise?
Just wondering if a rectal surgery is on the cards.
Best wishes
Sandra
gillian97397 sandra2468
Posted
I haven't been on the site for a long time, but am back here looking for more answers.
I have multiple problems which started 5 years ago,when I felt my bowel was prolapsing. On investigations it was discovered that I had divertivula disease, IBS, a very weak anal sphincter, an intussusception, vaginal vault prolapse and rectocele. I had suffered from incontinence on & off for years but had self treated with loperamide. Like everyone else on here, had terrible accidents all over the place, and had to take spare underwear with me.
The vaginal vault prolapse and rectocele were repaired, but for some reason they didn't do anything about the intussusception. After a year of tibial nerve stimulation,anal plugs (which fell out) and irrigation twice a day they implanted a neurostimulator, and things improved. That was 18 months ago, but I still have leakage, and the constant feeling that something is falling out of my bottom which is being caused by the intussusception. My original surgeon refused to do anything about it so I got a second opinion and he was more positive until he got the results of the CT scan, and on Monday he told me it was very very risky surgery because of the leads in my sacrum. So I now have to make decisions. Do I live with what I have, which is affecting my day to day life dreadfully, or do I have the stimulator removed, and see what happens. The surgeon has left the choice to me.
Yesterday I switched the stimulator off, and I'm not having a good day, but I don't know if its due to the prolapse or the lackof stimulation.
A warning too to anyone considering SNS. It has caused dreadful problems as far as getting MRI scans is concerned. I needed on for my head (which is allowed) but had to phone 5 hospitals before I could find one that had the right euipment to do it.
sandra2468 gillian97397
Posted
Just seen your message.
What surgery does your second opinion doctor propose?
Sandra