Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Lettuce For Lunch At Hospital Event.


Monklady123

Recommended Posts

Monklady123 Collaborator

I'm doing a fellowship at a local hospital, two semesters. We finished the first semester this past week and we had a small "graduation" service. (a few people are not continuing on to the next unit.) Lunch was part of it. So a few weeks ago the director of program asked me what I wanted to eat for the lunch. He said that the director of the food service said I could have whatever I wanted.

Well, that sounds nice but truthfully, based on what I've seen in the cafeteria, I wouldn't trust anything they put in front of me. So I said "oh don't worry, I'll just bring my lunch." (with really is okay with me, I am not AT ALL offended by bringing my own food). He didn't like that idea. So he started quizzing me on what I can and cannot eat.

So earlier last week he told me that the food service director was "working it out, it will be fine, they'll just give you the gluten free part of whatever they serve." yeah, okay.

Well, the lunch was chicken caesar salad. There was one bowl without the chicken or croutons. It was just plain lettuce! :lol: :lol: :lol: They also had a fruit plate and a raw veggie and dip plate. They had two kinds of salad dressing, plus the dip. But no signs about ingredients in the dressings.

But, of course I'm smart after being gluten free for more than a year now. I just whipped out my lovely lunch -- leftover chicken parmesan with rice noodles, and a yogurt. I had heated the chicken before I came upstairs so it was nice and hot. In fact, the room we were in was kind of chilly and I think my warm chicken was nicer than their cold salad. :P

But, what was most interesting was my conversation with our director. This is a program for chaplains and pastoral counselors, so in our class sessions they are always asking us "how do you feel about that." :rolleyes: So when the director starting fussing about my plate of lettuce and how I'm having to bring my own food and blah blah blah I asked him "why does it bother you so much that I can't eat what you're eating? I've told you that it bothers me not at all to bring my own. In fact I prefer it because then I know I won't get sick. So why does it bother you?" :lol: :lol: :lol:

He didn't really have an answer but he did stop bugging me about it. I enjoyed my lovely chicken parmesan. B)


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



Takala Enthusiast

LOL ! A bowl of lettuce, AGAIN! Anonymous salad dressings and a communal dipping area ! :lol::blink:

so why does it bother you?

Because he was a male and he assumed he could just somehow order something to be done, and he had come up short on his "effort" :rolleyes: anyway, and you have done a successful work - around anyway. Perhaps in his culture you are supposed to graciously accept that lettuce, and then not only be hungry the rest of the day but sick tomorrow.... Maybe he should be thinking about the patients, the poor celiac and gluten intolerant sick people who must sometimes cross the doorway of said facility.... here, have some lettuce, again! :P

pricklypear1971 Community Regular

We are taught to be good hosts/hostesses. A good hos/hostess will make their guests feel comfortable and well fed. That's why it bothers people.

I think what us food challenged people forget in this whole mix is that WE are comfortable bringing our food because we know how impossible it is to make "safe" food; however, the uninitiated don't truly understand this.

Perhaps we need to approach our explanation differently?

"Thank you for being so concerned about my comfort. However, my food intolerances are so severe and difficult to work around, and the consequences of error so severe that I would be more comfortable bringing my own food. I hope this doesn't upset you, because I am really looking forward to the event and seeing everyone."

I guess my point is that people WANT to accommodate you. They just don't understand they probably can't, regardless of good intentions.

I struggle with this, also.

Monklady123 Collaborator

Yes, I do understand about people wanting to accommodate us. And food is so much a part of being "hospitable". But what gets me is that this is a hospital! I've only been gluten free for a bit more than a year so I've never had experience with a hospital since my diagnosis. I guess I just expect hospitals to be experienced in diet for various conditions. When I expressed that to a friend who is also gluten free she said "yeah? well think again." :rolleyes:

pricklypear1971 Community Regular

Yes, I do understand about people wanting to accommodate us. And food is so much a part of being "hospitable". But what gets me is that this is a hospital! I've only been gluten free for a bit more than a year so I've never had experience with a hospital since my diagnosis. I guess I just expect hospitals to be experienced in diet for various conditions. When I expressed that to a friend who is also gluten free she said "yeah? well think again." :rolleyes:

Exactly. Think again.

You know the other place I find no help? Vegetarian restaurants. They are so consumed with keeping meat out, and subbing there's tons of processed stuff in there and a lot of it contains glutenous grains. And if it isn't processed it's a "whole grain" of some sort... Grains shoved in wraps, grains shoved in salads, grains inevitably shoved up my a$$....

I'm better off in a butcher shop. Or even an Italian restaurant.

Skylark Collaborator

Way to go! I love your question "Why does it bother you so much that I can't eat what you're eating?"

Glad you were smart enough to bring your lunch and didn't get stuck eating CC'd lettuce!

Strawberry-Jam Enthusiast

it's the opposite here... the most allergy friendly restaurant I found in Dublin is a veggie, mostly vegan place with tonnes of coeliac options and staff knowledgeable about the ingredients in the food. they make really creative dishes, rotate their menu regularly... they use a lot of soya, but I can always find several options that work for my gluten-, dairy-, and soya-free self.

I do find that a lot of health food stuff is packed full of whole grains, tho, spelt EVERYWHERE, soya everywhere... and dang if the spelt isn't always confusingly placed with or nearby to the gluten-free stuff.


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



pricklypear1971 Community Regular

it's the opposite here... the most allergy friendly restaurant I found in Dublin is a veggie, mostly vegan place with tonnes of coeliac options and staff knowledgeable about the ingredients in the food. they make really creative dishes, rotate their menu regularly... they use a lot of soya, but I can always find several options that work for my gluten-, dairy-, and soya-free self.

I do find that a lot of health food stuff is packed full of whole grains, tho, spelt EVERYWHERE, soya everywhere... and dang if the spelt isn't always confusingly placed with or nearby to the gluten-free stuff.

Don't you love it when they put the gluten-free stuff in a freezer next to the sprouted whole grain stuff??? Or gluten-free baked goods next to frozen cakes? Omg, gives me the willies.

Know of one restaurant that does vegan, gluten-free, and veg along with "regular". I've found if a place does vegan they are more likely to do gluten-free. But no vegan = grains everywhere. Why, I don't know....

Takala Enthusiast

Grains shoved in wraps, grains shoved in salads, grains inevitably shoved up my a$$...

Oh, thanks. Now I'm laughing so hard I have half chewed apple slices up my nasal cavities. My spouse kept buying these freaking ^%$#@(*&%^$ "organic" "natural" condiments because they said "naturally gluten free" on them, and I kept rejecting them, because it's a bad company for c'c, and they kept changing their ingredients, so he said "oh, it's okay, I'll just eat them." So I found out last weekend he has been using one of these same bottles the entire time on everything. Like glopping it on the hamburgers. Because I find the near empty bottle of rejected, condiment with grain vinegar shoved back in behind the other stuff and the regular condiment (Not Bleeping Organic, but much more likely gluten free) has not gone down at all, on the shelf of the refrigerator. I used my marking pen in a politically incorrect way on that situation. :angry:<_<

mamaw Community Regular

You go girl---- kudos to you.......

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,188
    • Most Online (within 30 mins)
      7,748

    Leeila
    Newest Member
    Leeila
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Ginger38
      So I recently had allergy testing for IGE antibodies in response to foods. My test results came back positive to corn, white potatoes, egg whites. Tomatoes, almonds and peanuts to name a few.  I have had obvious reactions to a few of these - particularly tomatoes and corn- both GI issues. I don’t really understand all this allergy versus celiac stuff. If the food allergies are mild do I have to avoid these foods entirely? I don’t know what I will eat if I can’t  have corn based gluten free products 
    • Kris2093u4
      Geography makes a difference.  I'm in the West and Trader Joe's gluten-free bread tastes great and is a better price than most gluten-free breads sold elsewhere in my area.  
    • JForman
      We have four children (7-14 yo), and our 7 year old was diagnosed with NCGS (though all Celiac labs were positive, her scope at 4 years old was negative so docs in the US won't call it celiac). We have started her on a Gluten Free diet after 3 years of major digestive issues and ruling out just about everything under the sun. Our home and kitchen and myself are all gluten-free. But I have not asked my husband/her dad or her other siblings to go completely gluten-free with us. They are at home, but not out of the home. This has led to situations when we are eating out where she has to consistently see others eating things she can't have and she has begun to say "Well, I can't have <fill in the blank>...stupid gluten."  How have you supported your gluten-free kiddos in the mental health space of this journey, especially young ones like her. I know it's hard for me as an adult sometimes to miss out, so I can't imagine being 7 and dealing with it! Any tips or ideas to help with this? 
    • Jane878
      By the time I was 5 I had my first auto0immune disorder, Migraine headaches, with auras to blind me, and vomiting, sensitivity to light and sound. I was 5 years old, and my stepfather would have pizza night, milling his own flour, making thick cheesy gluten pizza, that I would eat and the next day, I would have serious migraines, and my mother & stepfather did nothing about my medical problems. When I was 17 in my first year at college, I was diagnosed with my 2nd known auto-immune disorder, Meniere's disease. I was a elite athlete, a swimmer, and soccer player. And once again my parents didn't think anything of understanding why I had a disorder only older people get. Now after my mother passed from Alzheimer's disease she also suffered with living with gluten. She had a rash for 30 years that nobody could diagnose. She was itchy for 45 years total. My brother had a encapsulated virus explodes in his spleen and when this happened his entire intestines were covered with adhesions, scar tissue and he almost lost his life. He has 5 daughters, and when I finally was diagnosed after being pregnant and my body went into a cytokine storm, I lost my chance to have children, I ended up having Hashimoto's disease, Degenerative Disc disease, and my body started to shut down during my first trimester. I am 6ft tall and got down to 119lbs. My husband and I went to a special immunologist in Terrace, California. They took 17 vials of blood as we flew there for a day and returned home that evening. In 3 weeks, we had the answer, I have Celiac disease. Once this was known, only my father and husband made efforts to change their way of feeding me. At the family cabin, my stepfather & mother were more worried that I would ruin Thanksgiving Dinner. It wasn't until one of my cousins was diagnosed with Celiac disease. They finally looked into getting Gluten Free flour and taking measures to limit "gluten" in meals. He did nothing but ask for me to pay for my own food and wi-fi when I came to the cabin to stay after our house burned down. When he informed my mother, they proceeding to get into a physical fight and she ended up with a black eye. The is just more trauma for me. Sam had no interest in telling the truth about what he wanted. He lied to my mother that he had asked my husband if I could pay for "food" when he asked Geoffrey if I had money to pay for my wi-fi. My mother hates when he spends so much time on the computer so he lied and said I could pay for my own food. I will remind you I weighed 119lbs at this time. (At 6ft) that is a very sick looking person. Neither parent was worried about my weight, they just fought about how cheap my stepfather was. As my mother was diagnosed with Alzheimer's disease in 2014. He had her sign over the will to a trust and added his children. He had no testimonial capacity at the time, so she signed without proper papers. Making this Trust null and void. When I gave my brother my childhood home, my mother stated I would be getting an equal part of inheritance to the house on Race. It currently worth 2.0 million $. I got nothing, and my stepfather has since disowned me b/c of my claim and he knows that my mother would never have left it uneven between my biological brother and myself. She sat me and my husband down, as we lived at the Race Street house and treated and took care of it as our own. My brother took over b/c he was going through a horrific divorce and needed a home so he could get a better custody deal with his soon to be ex-wife who was a Assist DA for Denver. She used the girls against him, and he & I were the primary caregivers. We, Judd and I spent the most time with them pre the divorce. Once Judd moved into the house, he threw all of my mother, grandmother and my family heirlooms out to the Goodwill. Nobody told my mother about this as she was going through cancer treatment and had Alzheimer's disease in her mother and her sister. My stepfather and biological brother took advantage of this matter, as I called a "family council" that my brother just never could make it to at the last moment. All of the furnishing, kitchen ware, everything was in the house my brother just moved into. He had had 2 weddings, I chose to elope b/c my stepfather ruined my brother's first wedding by talking about his relationship with my brother in front of my dad and his entire family, insulting him and having my grandfather leave the ceremony. It was a disaster. My stepfather just plays dumb and blames my father for the slight. I was the only child not to have a wedding. So, my mother and stepfather never had to pay for a thing. My mother had had an agreement with my father he'd pay for college and all medical issues with their kids, myself and Judd. So truly my mother never had to pay for anything big for me in her entire life. I am looking for anyone that has had a similar story, where they grew up in a household that had a baker that regularly milled flour and ate gluten. What happened to you? DId you suffer from different auto-immune diseases b/c of living with a baker using "gluten" Please let me know. I have been looking into legal ways to get my stepfather to give me what my mother had promised, and he erased. Thank you for listening to my story. Jane Donnelly  
    • trents
      Possibly gluten withdrawal. Lot's of info on the internet about it. Somewhat controversial but apparently gluten plugs into the same neuro sensors as opiates do and some people get a similar type withdrawal as they do when quitting opiates. Another issue is that gluten-free facsimile flours are not fortified with vitamins and minerals as is wheat flour (in the U.S. at least) so when the switch is made to gluten-free facsimile foods, especially if a lot of processed gluten-free foods are being used as substitutes, vitamin and mineral deficiencies can result. There is also the possibility that she has picked up a virus or some but that is totally unrelated to going gluten-free.
×
×
  • Create New...