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Gluten Free Food In The Hospital?
#1
Posted 23 September 2012 - 06:50 PM
#2
Posted 23 September 2012 - 06:57 PM
You could talk to the dietary staff ahead of time. If it were me, I wouldn't want to add a gluten reaction to all of the just had a baby stuff. Its probably only 3 meals anyway.
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#3
Posted 23 September 2012 - 07:09 PM
#4
Posted 23 September 2012 - 07:10 PM
Can they do that? I never eat anything that ANYBODY has cooked. I am so scared about having the baby! It is number 5 for us though so Dh can't take care of the others plus bring me food three times per day (hospital is 1 hour away) So what should I do? Any advise? I know my doctor said he would "order" me a gluten free diet but what about cross contamination?
gluten-free since July 8, 2009!
#5
Posted 23 September 2012 - 07:16 PM
For the big day (I'm due Nov. 6), I will definitely bring some of my own food, but my hospital is able to provide gluten-free food too. I double-checked when they dropped it off and it said gluten-free on the paper that came with the meal.
That's awesome to hear. I plan to contact the hospital and maybe even run by and talk to the people in the cafeteria to see what options I have. Maybe if I do my homework now, my sister in law can push them to order some stuff if they don't have a lot.
#6
Posted 23 September 2012 - 07:33 PM
Much safer and you won't stress.
Probable Endometriosis, in remission from childbirth since 2002.
Hashimoto's DX 2005.
Gluten-Free since 6/2011.
DH (and therefore Celiac) dx from ND.
Responsive to iodine withdrawal for DH (see quote, above).
Genetic tests reveal half DQ2, half DQ8 - I'm a weird bird!
#7
Posted 25 September 2012 - 09:51 PM
I plan to pack some food items for me and will certainly contact the hospital cafeteria to see what can be offered safely.
Celiac disease(positive blood work/biopsy- 10/2008), gluten free oat intolerent, Hashimoto's Thyroiditis/Disease, Raynaud's Disease
DS2(age 8):
celiac disease(positive IgA tTG, no biopsy- 11/2010)
DS1(age 12):
repeated negative bloodwork and negative EGD/biopsy. Started on a gluten free trial(8/2011). He has decided to stay gluten free due to all of the improvements he has experienced on the diet.
#8
Posted 26 September 2012 - 02:04 AM
#9
Posted 26 September 2012 - 07:31 AM
"Everything that can be counted does not necessarily count; everything that counts cannot necessarily be counted." - Albert Einstein
"Life is not weathering the storm; it is learning to dance in the rain"
"Whatever the question, the answer is always chocolate." Nigella Lawson
------------
Caffeine free 1973
Lactose free 1990
(Mis)diagnosed IBS, fibromyalgia '80's and '90's
Diagnosed psoriatic arthritis 2004
Self-diagnosed gluten intolerant, gluten-free Nov. 2007
Soy free March 2008
Nightshade free Feb 2009
Citric acid free June 2009
Potato starch free July 2009
(Totally) corn free Nov. 2009
Legume free March 2010
Now tolerant of lactose
Celiac.com - Celiac Disease Board Moderator
#10
Posted 26 September 2012 - 10:03 AM
The dietician I consulted with after I was diagnosed just read off things from a pamplet and when I pointed out several mistakes she said that it seemed like I already knew enough. Didn't even mention the whole CC issue. Luckily my insurance paid for it cause it really wasn't worth my time. I know there are better ones out there though.If you could manage it, I would recommend talking to the dietician ahead of time. I know, I know, some of them are hopeless about gluten; and you probably can't hope to luck out like I did (the dietician was a celiac), but they can help you and talk to the kitchen staff and give them a brush up on gluten free. The hospital I was in did not have a gluten free menu but they did have Udi's bread (as a salt-free bread
) and the dietician made out a meal plan for me for every meal (and I was there three weeks!!). I ate a lot of salads with olive oil and balsamic vinegar, lots and lots of fruit and yogurt, sandwiches on Udi's, chicken and salmon with rice.
For me the biggest concern is getting CC'd from PO meds. I'm thinking my stay will be outpatient surgery so I can manage the food. I still plan on contacting the dietary staff just in case I have to stay overnight.
Celiac disease(positive blood work/biopsy- 10/2008), gluten free oat intolerent, Hashimoto's Thyroiditis/Disease, Raynaud's Disease
DS2(age 8):
celiac disease(positive IgA tTG, no biopsy- 11/2010)
DS1(age 12):
repeated negative bloodwork and negative EGD/biopsy. Started on a gluten free trial(8/2011). He has decided to stay gluten free due to all of the improvements he has experienced on the diet.
#11
Posted 06 November 2012 - 12:47 PM
If you could manage it, I would recommend talking to the dietician ahead of time. I know, I know, some of them are hopeless about gluten; and you probably can't hope to luck out like I did (the dietician was a celiac), but they can help you and talk to the kitchen staff and give them a brush up on gluten free. The hospital I was in did not have a gluten free menu but they did have Udi's bread (as a salt-free bread
) and the dietician made out a meal plan for me for every meal (and I was there three weeks!!). I ate a lot of salads with olive oil and balsamic vinegar, lots and lots of fruit and yogurt, sandwiches on Udi's, chicken and salmon with rice.
I called and talked to them and she said she had no doubt they could handle getting food for me that I could have as they are a 24hour room service type thing...I still doubted...So I tried to explain more...lol...she said If i will get her a list of foods I like (gluten free) that she will go herself and buy them to have on hand for me. But that still doesn't rule out cross contamination....Apparently when I eat gluten, I know while it is still in my mouth, as my mouth and throat starts burning right away. And I get a headache right away and gassy belly......So I might try it but if that happens, skip the meals and have my husband bring me food. But oh I don't want to learn the hard way
#12
Posted 06 November 2012 - 08:23 PM
#13
Posted 08 November 2012 - 02:45 AM
When my mother had open heart surgery 2 yrs. ago. The food was horrible and she wasn't really hungry anyway. So the dietician came up to see why she wasn't eating. My mom told her that she was having a hard time eating, but maybe if she could just have bowl of mashed potatoes that would go down well. At that point the dietician informed her, that no she couldn't eat potatoes, they contained gluten! LOL
If they were instant they could have. I don't know of any at the moment that do but when my daughter was diagnosed some years ago, some brands did.
#14
Posted 08 November 2012 - 02:47 AM
#15
Posted 08 November 2012 - 04:18 AM
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