Hi needing advise as soon as possible. I had a blockage Tuesday night the 5th which landed me in the hospital for 3 days. They did a CT with contrast, a couple Xrays and determined I had a high grade partial SBO. They did an NG tube and I was released on Friday on a liquid diet, which did that day and Saturday. Yesterday started small amount of soft solids but my concerns are I've had very watery stools since Tuesday and I get a bit nauseous, even when I haven't eaten anything. I'm assuming I still have a bit of a blockage. Should I go back to all liquid? I'm very concerned about the amount of weight I'm loosing and dehydration. I have a follow up with the GI on Wednesday. Thanks!
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So sorry this happened!! From my experience I would add Greek yogurt and a couple 30gr Premier Protein/day for strength and to retain your muscle mass. I continue with this even after my total blockage and 5 day hospitalization . I simply use half or whole Imodium to slow down diarrhea. Also drink electrolyte drinks like Propel for electrolyte replacement. Mashed Potatoes and Mac and cheese from Bob Evans are easy to digest and add lots of calories. I also add any cream soup like chowders, cheddar soup, mushroom soup but not the broccoli! Continue to give your system a break until you heal . My thoughts are with you.🥰
Thank you for your response! The protien shakes are a good idea. I've been somewhere in between full liquid and soft foods. How long did you have to do that for? I'm scared to use immodium as I know it has the potential to make a blockage worse.
Hey, wanted to check in, how are you???
Hi @Lauren Of Emerald City! I'm doing better. It cleared up a couple days later, but still freaked out. Haven't had a blockage in years. They think it's due to inflammation in my pouch, which I have chronic pouchitis that I've never been able to fully control
That makes sense!!! Inflammation can definitely do that! I am happy you are better!!! Do you think you may want to try biologics for your pouchitis one day???
I have tried them. I did Entyvio (didn't work), Remicade (which I had antibodies to since I used it 14 years ago for UC) and now Stelara (which currently hasn't been helping so far)