Dealing with Intestinal Adhesions After Colostomy Surgery

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911
soupflood1
May 22, 2025 12:06 am

Three weeks ago, I started feeling very bad, with vomiting after every meal or drink. This was happening seven months after my colostomy surgery.

After a week of daily vomiting, I became so weak that I passed out just before entering the taxi that was going to take me to the ER. Thank God for my wife, who helped me through all that.

I entered the ER with hyponatremia (low sodium in the blood, or low electrolytes in the blood) because of all the vomiting.

After an X-ray and an MRI, doctors decided I should get operated on because of intestinal adhesions from the previous colostomy surgery. All went relatively well until now; I'm still recovering as this second surgery was essentially the same as the first one, except for the cutting and pulling of the colon out.

The message I want to relay is this: if you are programmed for a colostomy, try to get an anti-adhesions gel or substance that the surgeon(s) can put inside your abdomen before closing it, in order to minimize the formation of such unwanted adhesions in the future.

In addition to that, leaving the draining tube in for a week or so more after leaving the hospital may also help, as could physiotherapy (abdominal massage). A private doctor told me this; he said that the draining tube should be left in until there is no more liquid draining through it (because the wound will heal while there will still be liquid needing to come out).

In my case, the surgeon removed the draining tube three days after surgery, and it turned out that half a cup of yellowish liquid started bursting through one of the stitches on my abdomen surgery eleven days after surgery.

If you're not sure that what I said is true, just ask your surgeon about it - I don't really know if it is true or not either, but one thing I know now is that I really, really don't want a third adhesions-removing surgery.

God bless.

ron in mich
May 22, 2025 12:50 pm
Very helpful

Hi Soup, about a year and a half after my first surgery, I had the same symptoms as you: throwing up and severe pain, and it was due to adhesions constricting the small bowel. After each surgery, he left the bottom inch open to drain during healing, and as you said, the surgeon told me he lubed up my innards so they wouldn't stick together anymore.

Posted by: w30bob

Hi gang,

I was thinking what a great resource this site has been for me since I found it. It would have been really helpful, but maybe a bit scary, to have found it before my ostomy, but that's water under the bridge. But I got thinking about it, and now I'm questioning why doctors and hospitals don't provide this site's contact info to any patient even considering an ostomy today. And how can we change that so potential ostomates can learn about the road ahead for them by getting on here and asking questions before the docs go chop-chop. How exactly do you get all hospitals to provide their patients specific information, like this website?

I just happened to find this site something like 4 years after my ostomy when I Googled "ostomy forum" or something like that. But I never found it during previous searches.....so I found this site pretty much by pure luck. We need to find a way to make this site available to new or soon-to-be ostomates......as that's when we really need to commiserate with fellow ostomates. Anybody have any thoughts on how we do this?

Thanks,

Bob

soupflood1
May 25, 2025 9:36 pm

My surgeon told me they cut the adhesions but didn't mention anything about lubing or putting an adhesions-deterring substance inside my abdomen. Hopefully, this was my last adhesions-related problem.

soupflood1
Jul 20, 2025 4:24 pm

Just had my third adhesions surgery 11 days ago, getting tired of this but have to press on.

I hope this was a "rectification" surgery and that it was the last.