New ileostomy

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7
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128
dianamkruger
Dec 13, 2025 6:38 pm

Looking for some experienced feedback on the output of my new ileostomy. I have had a colostomy for the last year, so not new to the bag experience. Just very different output. How much Imodium do you take? Should you worry about total liquid output, even when you are hydrating a lot? Do you measure your output? Doc says no more than 1200ml daily, but measuring Ugh! Are you super careful about your diet?

TJT6768
Dec 13, 2025 8:03 pm

I'm a newish one but I'm an ileostomy kinda guy.. lol

As for measuring, oooh no.. I really don't like that idea.

I can't advise on this I'm afraid but wanted to say I hope you get some answers soon, I'm sure you will. There are so many folks here willing to help and share their knowledge.

Be safe and well

Tony☺️

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

TJT6768
Dec 13, 2025 8:05 pm

Sorry.. just noticed in your header it is ileostomy.. do you have both colostomy and ileostomy?

Either way, the best of luck my dear

Tony

Yrsae67
Dec 13, 2025 8:06 pm

Hi Diana, that's a lot of questions, and I'll try to answer them.

The amount of output. You can measure how much water goes into a stoma bag. Think about the level at which you empty the bag, then you can roughly measure your output.

Foods to thicken: bananas, whole-wheat bread without whole seeds, crackers. Drink water with it, or tea.

Watch your salt intake. Use a bit extra salt if your output is very watery. For example, eat a slice of whole-wheat bread with a boiled egg and a little salt.

Drink a sports drink that contains both salt and sugar if you feel very weak.

Avoid mushrooms; they're like sponges and can cause constipation. Avoid stringy vegetables, such as sauerkraut or celery, or chop them very finely.

No more than a handful of nuts at a time. Chew everything thoroughly.

Tip: fat slows down the metabolism, so choose something like full-fat quark if your output is very watery.

Imodium. When the tips don't work, start with one tablet and see how your body responds to that. Good luck, i hope these tips help a little.

xnine
Dec 13, 2025 8:58 pm

Take an empty bag and fill it with water to a level where you usually have out put. That should give a number you can use without the mess.

 

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TerryLT
Dec 13, 2025 10:29 pm

Hi, fellow ileostomate here. I don't take Immodium, but I know many do. I use foods to slow down and thicken my output, bananas, peanut butter, both at breakfast, as that seems to be when my output is loosest. How much to hydrate depends on body size, etc., but remember your pee should be clear or just slightly yellow. If there is any more colour to it, you aren't hydrating enough. Also remember you need to add electrolytes, not just drink plain water. There are various ways to do this. I have a powdered electrolyte solution that I add to water and sip all day. It's not necessary to measure your output unless your doctor has specifically requested it for some reason. As far as diet goes, everyone is different and a lot depends on why you became an ileostomate. I started with a colostomy too, then got the ileo. I eat all the same foods and don't restrict myself from anything, but I make sure to chew really really well, and of course stay hydrated. Some ileos have to restrict their diets more. The only way to find out is to try all foods by introducing them slowly in small amounts to see if you can tolerate them. It may be a slow process, but why restrict yourself from eating things you love if you don't have to?

Terry

Mysterious Mose
Dec 13, 2025 10:32 pm

Yrsae67 gives some solid advice. Here are my 2 cents (which I guess no longer means anything here in the centless US).

Personally, I take 5mg of loperamide every night an hour before bed. Don't bother with Immodium or others that are the same. The anti-gas stuff doesn't do you any good. And it's more expensive. I buy my loperamide at Costco, where it is $0.99 for a box of 24 tablets.

My output is seldom "liquidy", as I take the loperamide and I eat a lot of fruit. My breakfast consists mainly of a smoothie made with blueberries, blackberries, raspberries, strawberries, and bananas. My pouch does sometimes get a little slushy when I get carried away with eating things like grapes. I also drink a lot of water. But, the consistency you are shooting for is that of oatmeal.

In my opinion, measuring your output is like counting how many times you empty your bag. It's a trap. Your output is going to vary and you will get a feel for it eventually. Since I drink a lot of water, I pee a lot. I tend to empty my bag whenever I urinate and am at home.

One of the bigger changes I have had to make is in my diet. I no longer eat anything that has any corn or corn byproduct in it. Particularly in the evening. One thing I hate is waking up in the middle of the night or morning with a rock-hard bag attached to my belly. As I get older, gas is more and more of a problem. I also avoid any and all milk products, except for a quarter cup of yogurt in my morning smoothie.

I am one of the lucky ones. I can eat whatever I please. Nuts, seeded fruits, grapes, whatever. I probably could eat popcorn just fine, except for the fact that even 2-3 kernels of the stuff give me terrible gas (wind). Again, I think my age makes it worse. Just a sign that we tend to die from the inside out. 🤣

A lot of ileostomates here would have nightmares with my diet. I can even eat things like green beans, peas, and the like. But, I don't. Ileostomates do not benefit from insoluble fiber, so I avoid them. And, unfortunately, two of my favorite vegetables are broccoli and brussels sprouts. Oh, the gas!

The long and the short of it is, the diet of an ileostomate is one of trial and error. Changes are you can eat the same as you did with a colostomy. Except for that nasty gas stuff. When you have a functioning colon, you can often do something about gas. With an ileostomy, abstinence from gaseous foods is often a desirable thing. Over the past 3 years, I have found myself moving more towards a meat and fruit diet. Don't eat a whole lot of green veggies.

Daniel

Ebony&Ivory
Dec 14, 2025 11:18 am

I agree with Mysterious Mose for the most part. I’m an ileo and I gave up on most of my doctors recommendations because I realized that we ileos are not the same. We are individuals and what works for each of us is not the same.

I’m lucky I guess because I eat almost everything. How I know what I can’t eat is that I tried it. I also have crohn’s so that’s another consideration for me. When my crohns flares I get diarrhea and my output is like water. Oatmeal is a prebiotic that feeds healthy gut bacteria and I eat probiotics in the form of kombucha, non dairy yugurt, kimchi, regularly. I can usually get my diarrhea in check in a day or two. I don’t stop eating and will add ‘Garden of Life’ meal replacement to make sure I don’t get depleted. I also drink a LOT of water. I have had to go to the ER for IV fluids a few times but it’s been quite a while since I’ve had to do that.

For example I can’t eat fried food unless I cook it myself in fresh healthy oil like olive, avocado. This is because of the crohns. Oil that has been used over and over makes me ill.

These are things that work for me.

The point is it takes time to figure out what you can and can’t tolerate.

In the beginning I tried to do all of the recommended things but the doctors have a one size fits all perspective. They would get frustrated when their recommendations didn’t work for me. Because we’re not the same.

I’m willing to share my experience and trials and errors with anyone.

It took me years to figure out that I’m allergic to many adhesives and most ostomy appliances I’m allergic to. I constantly had peristomal skin irritation and pouches not sticking. I finally had a allergy test and found out that I have quite a few allergies. I had to figure out which ostomy products I wasn’t allergic to because they all use adhesive because they have to stick.

Like Daniel because I drink so much I go to the bathroom often for bladder or bag so I empty everything while I’m there.

My point is that we have to figure it out pretty much for ourselves.

Jo