Frequent Stoma Output After Sigmoid Colostomy

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251
Ojibwa
Aug 02, 2025 12:52 am

Having had a sigmoid colostomy in December, I have had no real issues until a couple of weeks ago. Now, every time I eat, within minutes, I begin production where I have to remove stool and many times replace the bag. I watch what I eat and avoid all the foods that diets suggest. Since this is a new development, I do plan to ask the gastroenterologist. I would have thought this was a function post-surgery, but not now. I am reading about short bowel syndrome, but I would think that wouldn't start 8 months post-surgery. It's exhausting cleaning 5-8 times daily. I am eating foods that are supposed to slow this, but it's still not working. I appreciate any comments and suggestions.

SusanT
Aug 02, 2025 1:32 am

I've had similar problems, massive highly liquid output.

Potatoes helped me a little; nothing else did squat. But it wasn't much. My problem seems to have improved a bit now that I'm off TPN. I can only guess that getting fewer IV liquids means I absorb more from the colon.

Push your doctor for answers. I was working on that, but I have some other complications that were distracting from the issue.

You might want to look into bile malabsorption syndrome. That was my working theory for myself.

Good luck! Let us know what the doctor says. You aren't the first person to come on asking about this kind of problem with a colostomy.

iMacG5

When I found this web site, I didn't think its name had anything to do with actually meeting an ostomate but I later learned there were some folks who did meet and develop relationships. How good is that? That wasn't my intention. I definitely didn't want anyone to meet me. I felt broken and wasn't prepared to express those feelings. I thought it was a place where ostomates wrote about themselves, posed questions, shared thoughts, told jokes and, sometimes, just vented. I thought of it as a community of folks with similar interests and various degrees of experience. Mostly I found some of the most caring, selfless, wise and understanding people I ever imagined. I was so impressed with some of the writings; not because of their literary value but the way in which they addressed such a very complex environment. I read hundreds of exchanges and admired the way folks cared for each other. I became hopeful with my own situation and looked forward to the next day's offerings. Certainly some contributors stood out with their experience or particular skills in addressing some things but it seemed like a total effort with synergistic results. I felt blessed to have found this site. I still do.
Mike

lclark5585
Aug 02, 2025 1:37 am

That happens periodically with mine, especially when I've been overheated or stressed out for several days. I don't understand how it happens, either. I've often wondered if it's related to liver function. I do increase electrolytes and lie down more until it stops. Hope you're feeling well soon!

Morning glory
Aug 02, 2025 1:57 pm

Welcome

Hugo
Aug 02, 2025 3:27 pm

I've had my colostomy for 14 months, and the same happens to me, often with no rhyme or reason. You may want to try taking Imodium. It usually works for me.

 

My Ostomy Journey: Ryan | Hollister

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yip.susan21
Aug 02, 2025 4:27 pm

There are two foods I've found that slow things down: I eat half a banana or a couple of slices of baked sweet potato before meals. And I'm on a no-sugar-added diet. (Which, as it turns out, helps on a lot of fronts, everything from gut to eyes, to teeth, to liver, to pancreas, and blood sugar.)

Jayne
Aug 02, 2025 4:54 pm

Side word to Susan .................... Good to learn you are off TPN .................. Aug 1st?

~ ~ ~ ~ ~ J ~ ~ ~ ~ ~

infinitycastle52777
Aug 02, 2025 6:39 pm

I agree with Hugo; try taking Imodium. It can slow down production. Sometimes you have to take it three times a day, an hour before meals. It worked for me when I first got my ostomy and had problems with my bag filling up too fast. I don't usually have that problem anymore, but when I did, that is what helped.