Managing Hydration with Ileostomy and Gastroparesis

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MagicofMania
Dec 20, 2024 7:07 pm

I’ve had my ileostomy for a week now and I’m still having a hard time keeping hydrated. It feels impossible because I also have gastroparesis and I feel like I’m eating all the time but still not enough. It doesn’t seem possible to sustain this once I go back to work. Does anyone have any tips for this?

warrior
Dec 20, 2024 7:18 pm

Hi, yes indeed. Tips were discussed many times and beaten to death on this topic. It is a very serious situation when you dehydrate.

I suggest going to the forums icon above if you can. Trending topics. Click. Grab a seat and some orange juice. It will be an eye-opening event to read.

Hydration is attainable. It's work, but then it becomes second nature.

What I'm hearing recently is kidney disease developing because of a lack of hydration.

Wow, right? Don't need that on top of everything else.

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 🫶🏼

Archielee
Dec 20, 2024 8:20 pm

It took a long time for things to balance out for me too. I also have an ileostomy, and I had gastroparesis. Certain foods and beverages cause more liquidy output, leading to dehydration. I avoid fruit juice, coffee, and tea as this causes more fluid output. Some types of artificial sweeteners cause this too. Figuring out foods and drinks that cause that has been key for me. I tend to rely heavily on foods that are thickening. Sometimes I eat marshmallows after eating a banana, applesauce, etc. And I make sure I have something starchy at each meal. It's taken me a long time to sort it out, but I was in the hospital for 4.5 weeks before I could actually eat, and then another week and a half while eating solid food. If you have a lot of liquid output, make sure to drink an electrolyte beverage to get hydration faster. Sometimes I make my own, or I dilute Gatorade, or use an electrolyte powder mix (low sugar). Keeping up with hydration is hard but important.

aTraveler
Dec 20, 2024 8:25 pm

You can get some ideas from this thread:

https://www.meetanostomate.org/discussion-forum/viewtopic.php?t=33610