Jump to content
  • 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

Lunch With Co-wokers


MollyG.

Recommended Posts

MollyG. Newbie

Hi, my name is Molly and I have been on a gluten free diet for only 2 months now. My problem is with my co-workers and going out to lunch everyday. Everyday my co-workers beg for me to go to lunch with them. I try to explain to them that I would rather eat in and eat food that I know if safe for me than chance getting sick. But they never understand. They are always upset that I do not want to go with them. How do I make them understand? I have told them that I am willing to go out with them once a week but that does not seem to be enough for them. I do not want to lose them as friends.

Does anyone know what is safe to eat at Quizno's? They seem to always want to go there. I know I probably could have a salad but what about the dressings? Is there a salad dressing that is usually safe when you to restaurants? I know when I got salad dressing at Subway it said that it contained modified food starch and I was told to avoid that.


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



Celiac.com Sponsor (A8-M):



tarnalberry Community Regular

Two options:

1. go with them but bring your own items to the restaurant, and explain to the manager that you have severe food sensitivities and cannot risk the cross contamination.

2. eat before or after, go with them and socialize, but only have water.

If they frequent a handful of places, you could try going in some time when they aren't busy and working with the chef to see if something can be developed for you. (They might be willing to do this for a repeat customer...)

XoHeatherxO Rookie

I am in a similar situation with friends who dine out often. I have gotten too sick too many times. Choose restrauntes you know....I find it is safe to get a baked potato if nothing else, alaso, Annies makes great gluten-free salad dressings and you can order them in small packets to keep in your purse (I always keep a couple with me just in case!) If I order chicken or anything I make sure it is not cooked in anything and ask that the grill (where my chicken is cooking) be covered with foil becacuse of my severe allergies. Best case scenario I dont have to go out, but I have come along way and it is comfortable for me to just go out and have a drink or a fruit salad or something, you have to do what's right for you! :D

MollyG. Newbie

I would like to thank you for your rely. I went to the Annie's website, but I did not see the small packets of salad dressing. I only saw that you have to order 6 bottles at a time! Where do you purchase these small packets? I would love to carry them in my purse instead of a bottle (I would have to start carrying a larger purse).

terri Contributor

I bought Annies from the Gluten free mall or the gluten free pantry. I carry them in my purse. I also work and found that the women I used to go out to lunch with I now tell them I'll go out to shop at lunchtime instead. I also take a yoga class twice a week at lunch and go out to eat maybe twice a month. Being sick at work stinks! Also there are so many places I won't go because of cross contamination like Subway, McDonalds, Panera, any Chinese restaurant , etc. that they have accepted that. If they don't then they are your real friends. Try to accomodate them 2 or 3 times a month but you pick the place. Just my thoughts...

celiac3270 Collaborator

First off, if they're real friends, they'll continue to be friends regardless of whether or not you choose to eat with them. Second, perhaps you could make a compromise. Read about which restaurants are gluten-free, do some research, and maybe next time, YOU choose where to eat out :) . I don't really like restaurants, either, and am anxious about put my health into their hands......

Anyway, good luck.

-celiac3270

flagbabyds Collaborator

You can always get a restaruant card and talk to the chef before you go, then when you go you will know what you can have and they will know what you dietary restrictions are and how to handle them instead of haveing to deal with an annoying waiter go befoere or call them and talk to the chef. Your friends should understand and if they are really your friends they will support you. You can also eat ahead of time or eat afterwards and only get fruit (that is almost always safe) and then just eat when you go back to work.


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



Celiac.com Sponsor (A8-M):



celiacfreeman Contributor

Lunch with co wrokers,

I really struggled with that, at first I went out anyway and found that by the time I explain my allergy and wait for special food, my lunch break was over before the speical food was prepared. Then I think that when co worker see your not going to comprimise your health, they understand why your sitting at your desk eating lunch as they trapse off to a resturant. I save eating out as a treat, as it is always a risk!!!!! It takes awhile to to get comfortable eating out. It's very very scary at first. I wouldn't recommend doing it right off after you diagnosed. You really don't know all the contaiments until you has hours and hours to study the diet.

My recommendation. Stay at your desk the first 90 days or so.

celiac3270 Collaborator

I agree with Celiacfreeman.......I wouldn't eat out in the beginning, either....then again, this is coming from someone who was never a big fan of restaurants to begin with :P . It is scary to put your health in the hands of others, especially in the beginning. I only trust my mom or myself to make a truly gluten-free meal..........and I'm gaining trust in my dad....but this is after months! To put this trust in someone who knows such a minimal amount about the diet is difficult...and scary. Your friends should, and, I hope, will understand if you don't go out to lunch with them. They're not the ones with health issues to worry about.

-C

tarnalberry Community Regular

A coworker's birthday was the other day, and we - on a whim - went to Chuck E Cheese. (He turned 33, what better thing to do when you turn 33 ;-). ) Anyway, I just had half the lunch I brought before we went there, and half when we got back. I enjoyed the conversation and the people (and the games), and it was just fine. If you are comfortable with the fact that you don't eat what other people eat and it won't upset you, then I'd recommend this method.

angel-jd1 Community Regular

I agree, eating out is not always about the food. Go and enjoy the company and conversation. You don't have to be a shut in just because you can't have gluten!! Enjoy live, just modify it.

-Jessica :rolleyes:

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - asaT replied to wellthatsfun's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      2

      nothing has changed

    2. - nanny marley replied to SilkieFairy's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      IBS-D vs Celiac

    3. - asaT replied to Scott Adams's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      45

      Supplements for those Diagnosed with Celiac Disease

    4. - par18 replied to Woodster991's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      9

      Is it gluten?

    5. - SilkieFairy replied to SilkieFairy's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      IBS-D vs Celiac

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,342
    • Most Online (within 30 mins)
      7,748

    Muhammad
    Newest Member
    Muhammad
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • asaT
      Scott, I am mostly asymptomatic. I was diagnosed based on high antibodies, low ferritin (3) and low vitamin D (10). I wasn't able to get in for the biopsy until 3 months after the blood test came back. I was supposed to keep eating gluten during this time. Well why would I continue doing something that I know to be harmful for 3 more months to just get this test? So I did quit gluten and had the biopsy. It was negative for celiacs. I continued gluten free with iron supps and my ferritin came back up to a reasonable, but not great level of around 30-35.  Could there be something else going on? Is there any reason why my antibodies would be high (>80) with a negative biopsy? could me intestines have healed that quickly (3 months)?  I'm having a hard time staying gluten free because I am asymptomatic and i'm wondering about that biopsy. I do have the celiacs gene, and all of the antibody tests have always come back high. I recently had them tested again. Still very high. I am gluten free mostly, but not totally. I will occasionally eat something with gluten, but try to keep to a minimum. It's really hard when the immediate consequences are nil.  with high antibodies, the gene, but a negative biopsy (after 3 months strict gluten-free), do i really have celiacs? please say no. lol. i think i know the answer.  Asa
    • nanny marley
      I have had a long year of testing unfortunately still not diagnosed , although one thing they definitely agree I'm gluten intolerant, the thing for me I have severe back troubles they wouldnt perform the tests and I couldn't have a full MRI because I'm allergic to the solution , we tryed believe me  I tryed lol , another was to have another blood test after consuming gluten but it makes me so bad I tryed it for only a week, and because I have a trapped sciatic nerve when I get bad bowels it sets that off terribly so I just take it on myself now , I eat a gluten free diet , I'm the best I've ever been , and if I slip I know it so for me i have my own diagnosis  and I act accordingly, sometimes it's not so straight forward for some of us , for the first time in years I can plan to go out , and I have been absorbing my food better , running to the toilet has become occasionally now instead of all the time , i hope you find a solution 🤗
    • asaT
      I was undiagnosed for decades. My ferritin when checked in 2003 was 3. It never went above 10 in the next 20 years. I was just told to "take iron". I finally requested the TTgIgA test in 2023 when I was well and truly done with the chronic fatigue and feeling awful. My numbers were off the charts on the whole panel.  they offered me an endoscopic biopsy 3 months later, but that i would need to continue eating gluten for it to be accurate. so i quit eating gluten and my intestine had healed by the time i had the biopsy (i'm guessing??). Why else would my TTgIgA be so high if not celiacs? Anyway, your ferritin will rise as your intestine heals and take HEME iron (brand 4 arrows). I took 20mg of this with vitamin c and lactoferrin and my ferritin went up, now sits around 35.  you will feel dramatically better getting your ferritin up, and you can do it orally with the right supplements. I wouldn't get an infusion, you will get as good or better results taking heme iron/vc/lf.  
    • par18
      Scott, I agree with everything you said except the term "false negative". It should be a "true negative" just plain negative. I actually looked up true/false negative/positive as it pertains to testing. The term "false negative" would be correct if you are positive (have anti-bodies) and the test did not pick them up. That would be a problem with the "test" itself. If you were gluten-free and got tested, you more than likely would test "true" negative or just negative. This means that the gluten-free diet is working and no anti-bodies should be present. I know it sounds confusing and if you don't agree feel free to respond. 
    • SilkieFairy
      I realized it is actually important to get an official diagnosis because then insurance can cover bone density testing and other lab work to see if any further damage has been done because of it. Also, if hospitalized for whatever reason, I have the right to gluten-free food if I am officially celiac. I guess it gives me some legal protections. Plus, I have 4 kids, and I really want to know. If I really do have it then they may have increased risk. 
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.