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

What Do You Say To The Server In A Restaurant?


MrsManners

Recommended Posts

MrsManners Newbie

What do you say to explain that you can't have gluten to a server or a chef in a restaurant? I need a script so tell me as if I were your server.

Also, do you use a restaurant card? If so, do you just give it to them or do you give it to them and then explain?

I work in sales and travel some so I'm going to be forced to eat out and I want to get it right. Thanks!


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



Celiac.com Sponsor (A8-M):



ShayFL Enthusiast

They have Triumph Dining Cards. But as I learned today....sadly....that you shouldnt just talk to the server. You MUST ask for the Manager. The Manger will make sure it is done right. Servers generally wont.

It is basically a crap shoot when your health is the hands of others. For instance, today, I ate out with my family. They miss it so and I wanted to feel "normal" for a day. So off to Cheescake Factory we went. I brought my own dressing and meat and dessert. Initially I was just going to get a salad and toss my own meat on it (I've done this before without issue). BUT I mentioned Celiac to the server and she said....oh...yes...our General Manager has Celiac so we are VERY AWARE and TAKE EVERY PRECAUTION. He eats here......I said...so you know I need fresh pans....YES....So I ordered sauteed spinach and asparagus cuz I had meat. So I am sitting there eating my asparagus and it dawns on me that I didnt say....no pasta water. When she check on us....I ask her if she made sure my asparagus was cooked in fresh water. Nope. She comes back and takes the plate away and says that ALL of their veggies are cooked in pasta water. mad.gif

Then the Manager comes to our table and asks who he just "poisoned". He knew of course knew the consequences. He felt terrible. Apologized profusely for his server not being trained well enough. So he paid for all of our food....about 60.00 worth for my DH and DD with dessert. Now....I wait.....and pray.......

MrsManners Newbie

I saw your post about that and it terrified me! I had no idea veggies were cooked in pasta water. Asking for the manager is a good idea - I'll make sure to do that.

babysteps Contributor
What do you say to explain that you can't have gluten to a server or a chef in a restaurant? I need a script so tell me as if I were your server.

Also, do you use a restaurant card? If so, do you just give it to them or do you give it to them and then explain?

I work in sales and travel some so I'm going to be forced to eat out and I want to get it right. Thanks!

Here is one person's protocol, at Open Original Shared Link - she is gluten-free, nut free, fish free, etc...

In general, 'chain' restaurants with gluten-free menus are okay.

'chain' restaurants w/o gluten-free menus are tough

'fancy' (make it themselves from scratch) restaurants are better than chains w/o gluten-free menus but it depends...check here or on your local celiac support group's site to find gluten aware restaurants to try

Cards can help. Chefs really DO appreciate it if you call ahead.

The more you eat out, the better you will get at communicating with the server & dealing with menus (I am now a menu gluten psychic, very good at guessing where gluten is least likely but I ALWAYS double check that it really isn't there).

When you get your food, if *anything* looks amiss, double check before touching it or taking a bite! If you don't feel comfortable that your server can handle your needs, talk to the manager or the chef. Or leave if it's really not working.

I have found that using open table (for restaurants that link to it) is effective, a note there that I am gluten-free is much more likely to reach the server than a note on a phone reservation in my experience.

check the travel and restaurant boards here for good tips, too. kenlove has had many very useful posts on this topic, try searching for those.

Good luck and happy eating!!

celiacsista Newbie

You need to make sure they "get it". If you feel uneasy or they seem annoyed or confused....go hungry and eat when you get home. I travel for work too. I usually just but some fruit and veggies, cheese and crackers. I used to get sick way too often. It is so not worth it.

I went out with a group last night. It was a set menu because of the size of the group. My sister and I both have celiac and called several days ahead to discuss the menu. We were presented with a gluten free menu that they had altered from the set menu. They seemed really on the ball. The side dishes were served seperately for everyone but the waiter assured us they were fine. I had an uneasy feeing when I saw the rice and green beans. Looked like there was soy sauce on them. So I asked. And there was. It is kind of scary to think they seemed so confident and sure our meal was gluten free but didn't even know there was wheat in soy sauce. It was a very high end restaurant too. If in doubt always, always ask.

I never even thought that vegetables would be cooked in pasta water. Wow! Scary.

curlyfries Contributor

I haven't eaten out much, but I hope this helps:

I tell the server I have Celiac disease, and could I please talk to the manager or chef about what is safe on the menu for me to eat. ( most managers have some idea about celiac, as do most chefs. Servers usually don't have a clue)

I usually have a couple of different ittems on the menu picked out, so I can get specific about what I want and how it can be modified.

I have Celiac disease, which means I will get sick if I eat anything with wheat , barley.........

How do you season your steaks?....or chicken or fish...

Do you use a cooking spray?....(some use Baker's Joy to prevent sticking...contains wheat)

Can you fix mine without seasoning?

Could you cook mine on a separate pan?...or put foil down on your grill?...( I had one restaurant say they couldn't)

How do you fix your veggies. Could you cook mine in the microwave?

I try to call ahead during a slow time of the day first. I research the restaurant by looking for their website and trying to find their menu.......gluten-free or regular, then googling the restaurant on celiac.com to see what others have experienced.

One time my company took us out to lunch to a steak place. I knew we would all be served the same thing, but didn,t know what that would be. I found out on this forum that their green beans were not safe, nor the seasonings on the meat. They coat their potatoes in bacon fat.

They were not open to regular customers during the day so didn't answer their phone. So when I got there I told the hostess I needed to talk to the manager, because I have Celiac disease (I always use the word "disease" cuz I figure they'll realize it's serious and not just some dietary fad) and there are certain foods that make me sick. He came to my table and we discussed what was to be served----chicken, green beans, and a baked potato. I asked him to have mine fixed without seasoning, with foil on the grill. I told him I couldn't have the green beans, so he offered a mixed vegetable. I said I can't have the bacon fat on the potato, so he had mine microwaved. (The potatoes were already cooked, so he had to get a fresh one for me.) I apologized for being such a pain :sweetsmile!: He was very nice and concerned that he did everything right. The manager oversaw my entire meal.

I'm sure others will think of things I have forgotten....but this is a start. Hence the reason I don't eat out much :P

frec Contributor

I am still really struggling with this issue! My first big hint is to hand them a list or card or something in writing. The long list scares them and it is usually noisy in restaurants. ("I can't eat wheat." "Oh, we have lots of vegetarian choices!") My other big hint is to use the term bare naked--I want just bare naked chicken. They are usually appalled by my terminology but they leave everything off.

I had no idea about the pasta water either. Ew.


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



Celiac.com Sponsor (A8-M):



babysteps Contributor

I usually say "I cannot eat anything with wheat, flour, barley or rye - this also means I cannot eat any bread, soy sauce or miso. Even a very small amount will make me very sick".

Again, if the server doesn't seem to get it - or doesn't seem to care - go to the manager or the kitchen. Generally, I have best luck with tiny family-run places or fancy/foodie places. Chains without gluten-free menus scare me the most, I'm not sure if anyone in the kitchen really knows what's in the food.

Most servers, and a fair number of kitchens, have no idea about wheat in soy sauce, much less barley in miso. Not that so many places use miso, but some of the 'fusion' type restaurants use it quite a bit.

Amazing how many folks then assume I cannot eat corn or rice...but most places after a few back-and-forths it eventually works out.

And I almost always have food with me - lara bars, nuts, something safe to tide me over in case it doesn't work.

frec, I like the "bare naked" term.

And yes the pasta water is something I would never have thought of, first heard about it on this forum a few months ago. Also always check about fried items, most of the time unless you are the first diner getting food after new oil -- some restaurants this is 2x/day, some it's hard to tell ;) -- the fry oil has already been used for everything (breaded/glutened and not)

One thing I look for is anything marked as 'sauted' or 'pan fried' or the word 'skillet' - often this means your dish is cooked in its own pan. Always ask to double check, though!!

other random thoughts on menu terms:

'braised' just means cooked with liquid (usually in oven, sometimes stove top), but *very* often there is a dusting of flour on the meat with this method, so generally I avoid it.

'crispy' almost always means breaded

'dusted' anything almost always means some flour dredging

'oven roasted' usually means cooked ahead of time, so it can be hard to alter such dishes if they aren't gluten-free in the first place

'rice pilaf' is often code for *there's pasta in this rice*

most any 'stuffed' item will have bread or breadcrumbs involved

'crab' often means sea legs, which have gluten. Best to ask both "is this sea legs" and if it's "all plain crab", not just if it's "real crab" (different regions call this different stuff - seafood salad, surimi are other terms I've seen)

Anyone else have favorite menu trigger words?

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. - tiffanygosci replied to tiffanygosci's topic in Introduce Yourself / Share Stuff
      1

      Celiac support is hard to find

    2. - trents replied to mamaof7's topic in Parents, Friends and Loved Ones of Celiacs
      1

      Help understand results

    3. - mamaof7 posted a topic in Parents, Friends and Loved Ones of Celiacs
      1

      Help understand results

    4. - Dizzyma replied to Dizzyma's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      3

      Newly diagnosed mam to coeliac 11 year old

    5. - tiffanygosci posted a topic in Introduce Yourself / Share Stuff
      1

      Celiac support is hard to find

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

    • Total Members
      132,955
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • tiffanygosci
      EDIT: I did find a monthly Zoom meeting for Celiacs through the Celiac Disease Foundation, so I'll be able to talk with some other people on January 15. And I also found a Celiac Living podcast on Spotify made by a celiac. I feel a little bit better now and I am still hoping I will find some more personal connections in my area.
    • trents
      Welcome to the celiac.com community, @mamaof7! It means for the one celiac disease antibody test that was ordered, she tested negative. However, other tests should have been ordered, especially for someone so young who would have an immature immune system where there would be a high probability of being IGA deficient.  The one test that was ordered was an IGA-based antibody test. It is not the only IGA antibody test for celiac disease that can be run. The most common one ordered by physicians is the TTG-IGA. Whenever IGA antibody tests are ordered, a "total IGA" test should be included to check for IGA deficiency. In the case of IGA deficiency, all other IGA tests results will be inaccurate. There is another category of celiac disease antibody tests that can be used in the case of IGA deficiency. They are known as IGG tests. I will attach an article that gives an overview of celiac disease antibody tests. All this to say, I would not trust the results of the testing you have had done and I would not rule out your daughter having celiac disease. I would seek further testing at some point but it would require your daughter to have been eating normal amounts of gluten for weeks/months in order for the testing to be valid. It is also possible she does not have celiac disease (aka, "gluten intolerance") but that she has NCGS (Non Celiac Gluten Sensitivity, or just "gluten sensitivity" for short) which is more common. The difference is that celiac disease is an autoimmune disorder that damages the lining of the small bowel whereas NCGS does not autoimmune in nature and does not damage the lining of the small bowel, though the two conditions share many of the same symptoms. We have testing to diagnose celiac disease but there are no tests for NCGS. To arrive at a diagnosis of NCGS, celiac disease must first be ruled out. A gluten free diet is the solution to both maladies.   
    • mamaof7
      For reference, daughter is 18 mths old. Was having painful severe constipation with pale stool and blood also bloating (tight extended belly.) Liver and gallbladder are normal. Ultrasound was normal. Dr ordered celiac blood test. We took her off gluten after blood draw. She is sleeping better, no longer bloated and stools are still off color but not painful.    "GLIADIN (DEAMID) AB, IGA FLU Value  0.84 Reference Range: 0.00-4.99 No further celiac disease serology testing to be performed. INTERPRETIVE INFORMATION: Deamidated Gliadin Peptide (DGP) Ab, IgA A positive deamidated gliadin (DGP) IgA antibody result is associated with celiac disease but is not to be used as an initial screening test due to its low specificity and only occasional positivity in celiac disease patients who are negative for tissue transglutaminase (tTG) IgA antibody."   Anyone know what in the world this means. She isn't scheduled to see GI until late April. 
    • Dizzyma
      Hi Trent and Cristiana, thank you so much for taking the time out to reply to me.  My daughters GP requested bloods, they came back as showing a possibility of celiac disease, she advised me to continue feeding gluten as normal and wait on a hospital appointment. When we got that the doctor was quite annoyed that the gp hadn’t advised to go gluten free immediately as she explained that her numbers were so high that celiac disease was fairly evident. That doctor advised to switch to a gluten-free diet immediately which we did but she also got her bloods taken again that day as it made sense to double check considering she was maintaining a normal diet and they came back with a result of 128. The hospital doctor was so confident of celiac disease that she didn’t bother with any further testing. Cristiana, thank you for the information on the coeliac UK site however I am in the Rrpublic of Ireland so I’ll have to try to link in with supports there. I appreciate your replies I guess I’ll figure things as we go I just feel so bad for her, her skin is so sore around her mouth  and it looks bad at an age when looks are becoming important. Also her anxiety is affecting her sleep so I may have to look into some kind of therapy to help as I don’t think I am enough to help. thanks once again, it’s great to be able to reach out xx   
    • tiffanygosci
      I have been feeling so lonely in this celiac disease journey (which I've only been on for over 4 months). I have one friend who is celiac, and she has been a great help to me. I got diagnosed at the beginning of October 2025, so I got hit with all the major food holidays. I think I navigated them well, but I did make a couple mistakes along the way regarding CC. I have been Googling "celiac support groups" for the last couple days and there is nothing in the Northern Illinois area. I might reach out to my GI and dietician, who are through NW Medicine, to see if there are any groups near me. I cannot join any social media groups because I deleted my FB and IG last year and I have no desire to have them back (although I almost made a FB because I'm desperate to connect with more celiacs). I'm glad I have this forum. I am praying God will lead me to more people to relate to. In my opinion, celiac disease is like the only food- related autoimmune disease and it's so isolating. Thanks for walking alongside of me! I'm glad I know how to help my body but it's still not easy to deal with.
×
×
  • 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.