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Hospital Food


Nor-TX

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Nor-TX Enthusiast

I am about to go into the hospital for a few days for a total knee replacement. After talking to the doctor and discussing the problems that I might face relying on the hospital food, he suggested I bring my own. The first day I will be on liquids and drugs :P, and the second day I assume will be soft foods. I plan on making jello, and bringing my own broth. I have made my own gluten-free, df granola bars but I think they may not be good until the 3rd day. I know I can take Udi bread/bagels, slices of ham or a cooked chicken breast, but I am having trouble thinking of what else. I have colitis so I can't do fresh vegetables or fruit, no dairy, no eggs, no spicey foods. I have several ideas, but I'm trying to think of light foods that I can cook before hand and aren't messy or "tummy stimulating". Just wondering what others have done when in the hospital?


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kareng Grand Master

Will the nurses or aides microwave in the breakroom for you? You could make some chicken & rice soup (or at our house its less soup more chicken & rice & cooked carots). A cooked hamburger to re-heat. Maybe some applesauce? Some noodles cooked in chicken or beef broth? Rice Chex straight from the box.

Do you have someone to bring food for you so you don't have to have it all on the first day?

Good luck with the surgery.

Nor-TX Enthusiast

Will the nurses or aides microwave in the breakroom for you? You could make some chicken & rice soup (or at our house its less soup more chicken & rice & cooked carots). A cooked hamburger to re-heat. Maybe some applesauce? Some noodles cooked in chicken or beef broth? Rice Chex straight from the box.

Do you have someone to bring food for you so you don't have to have it all on the first day?

Good luck with the surgery.

Chicken and rice soup is a good idea. Can't do hamburger meat - I probably won't be able to eat meat until I leave. Rice Chex is a good idea to munch on, thanks. I probably could get a plain whole baked potato from the hospital. Thanks for the ideas.

mushroom Proficient

Be sure to take your own spread from home. I would also take my own juice - the stuff I got offered was loaded with HFCS. Basically, don't trust anything that comes out of the kitchen because at least where I was the kitchen staff didn't even know what gluten was let alone how to avoid cross-contamination. They had menu plans for everything under the sun EXCEPT gluten-free. I had hubs bringing me stuff all the time and had my own section of the ward fridge. I am sorry you can't do yogurt and fruit because I survived a lot on that. You could keep some almond/hemp milk in the fridge :) I didn't have an opportunity to plan food in advance so had to temporize. Fortunately there was a Whole Foods close by. You might try calling the hospital and speaking with the dietitian (not that my conversation with her did much good) and at least find out what their awareness level is. But I wouldn't hold out a lot of hope (or trust) :rolleyes:

You could premake things like tuna casserole servings, or whatever other casserole-type things your food restrictions permit. I know that is what I craved in the hospital because I couldln't eat anything they made, and I seldom got more than a piddling little serving of cooked vegetables - one day they were "out" of vegetables altogether. You don't get health food in a hospital :o

freeatlast Collaborator

You might want to look at these sites and print out the food lists for the hospital staff:

https://www.celiac.com/articles/21740/1/Tips-for-Ensuring-a-Gluten-Free-Hospital-Stay/Page1.html

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    • trents
      You might consider asking for a referral to a RD (Registered Dietician) to help with food choices and planning a diet. Even apart from any gluten issues, you will likely find there are some foods you need to avoid because of the shorter bowel but you may also find that your system may make adjustments over time and that symptoms may improve.
    • Ello
      I wish Dr’s would have these discussions with their patients. So frustrating but will continue to do research. Absolutely love this website. I will post any updates on my testing and results.  Thank you
    • trents
      Losing 12" of your small bowel is going to present challenges for you in nutritional uptake because you are losing a significant amount of nutritional absorption surface area. You will need to focus on consuming foods that are nutritionally dense and also probably look at some good supplements. If indeed you are having issues with gluten you will need to educate yourself as to how gluten is hidden in the food supply. There's more to it than just avoiding the major sources of gluten like bread and pasta. It is hidden in so many things you would never expect to find it in like canned tomato soup and soy sauce just to name a few. It can be in pills and medications.  Also, your "yellow diarrhea, constipation and bloating" though these are classic signs of a gluten disorder, could also be related to the post surgical shorter length of your small bowel causing incomplete processing/digestion of food.
    • Ello
      Yes this information helps. I will continue to be pro active with this issues I am having. More testing to be done. Thank you so much for your response. 
    • trents
      There are two gluten-related disorders that share many of the same symptoms but differ in nature from each other. One is known as celiac disease or "gluten intolerance". By nature, it is an autoimmune disorder, meaning the ingestion of gluten triggers the body to attack it's own tissues, specifically the lining of the small bowel. This attack causes inflammation and produces antibodies that can be detected in the blood by specific tests like the TTG-IGA test you had. Over time, if gluten is not withheld, this inflammation can cause severe damage to the lining of the small bowel and even result in nutrient deficiency related health issues since the small bowel lining is organ where all the nutrition found in our food is absorbed.  The other is NCGS (Non Celiac Gluten Sensitivity or just "gluten sensitivity") which we know less about and are unsure of the exact mechanism of action. It is not an autoimmune disorder and unlike celiac disease it does not damage the lining of the small bowel, though, like celiac disease, it can cause GI distress and it can also do other kinds of damage to the body. It is thought to be more common than celiac disease. Currently, we cannot test for NCGS. Celiac disease must first be ruled out to arrive at a diagnosis of NCGS. Both disorders require elimination of gluten from the diet.  Either of these disorders can find their onset at any stage of life. We know that celiac disease has a genetic component but the genes are inactive until awakened by some stress event. About 40% of the general population has the genetic potential to develop celiac disease but only about 1% develop active celiac disease. The incidence of NCGS is thought to be considerably higher. I hope this helps.
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