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

Can I Trust gluten-free Items On The Menu?


lakegirl410

Recommended Posts

lakegirl410 Rookie

Hi Everyone,

I was just recently diagnosed with Celiac Disease. My husband and I used to eat out a lot, but now, we don't know where to go. If a restaurant does have a gluten free menu, can I trust that it's really gluten free? I am worried about cross-contamination. I imagine salads without croutons will be okay! Please help! I really appreciate any input! Thanks so much!!!


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



Celiac.com Sponsor (A8-M):



luvs2eat Collaborator

Whenever we go out, even to restaurants w/ gluten free menus and places we've been to before, we go out of our way to make friends w/ our server.... "Have a seat and let me tell you about my food needs." Ha ha. It helps that my husband is super friendly and we are always treated so well. I tell them about celiac disease and let them know just how important it is that saying "no croutons" is serious enough that if my salad comes out w/ croutons on it, I'll have no choice but to ask that the salad be tossed and made again... or the burger will have to be remade and not just lifted off the bun. Every single time, our servers go far out of their way to see that my food is done right. We tip well and thank them for their effort! I've spoken to managers several times about how well our servers have accommodated me.

I think you can trust the menu... but the handling of your food needs to be discussed w/ your server!

c12 Rookie

Most of the restaurants that offer full gluten-free menus are pretty good about making sure that your meal is safe. They print out a menu claiming that a meal is gluten-free if it isn't - that would be recipe for legal problems!

I've personally had GREAT experiences at PF Changs, the staff is so knowledgeable, so that could be a good one to try first, if you're nervous.

lovegrov Collaborator

If they have a gluten-free menu, I generally trust that because no place is going to claim gluten-free items and then poison you on purpose. But, wherever you go there's always the chance of CC, but you can cut down on that by trying to go at slower hours and, as mentioned before, by making friends with the server and/or the manager.

richard

Juliebove Rising Star

Oddly, I've found salads to be one of the worst things to order. You can tell them no croutons but often they will still be there. Worse yet, they will put them on them pick them off.

disgruntled Newbie

this is in response to lovegrov, i am trying to remain as anonamous(sp) as i can about this. i work for a restaurant company that the flagship (possibly only) concept is called fresh city. i am conviced the owners do not know what gluten free really means...on our menu board it lists the teriyaki sauce as gluten free an as i am sure many of you know it needs to be specially made for that to be true. i started researching this because of the fact that i had a geust send in an email and complain about me not wanting to get her that sauce for this reason.

the SECOND ingredient of the "gluten free" teriyaki sauce, happens to be soy sauce made from the traditional recipe (second most ingredient being wheat)

the owners want me written up and none of the other managers beleive me on this...soo i have spent the last two hours researching gluten and hidden gluten sauces.

to summarize this. DO NOT TRUST THE POSTED "GLUTEN FREE" MENU'S WITH SAUCES OR ANYTHING EVEN SLIGHTLY QUESTIONABLE.

PLEASE FOR YOUR OWN SAFETY.....I EMPLORE YOU.....ASK FOR AN INGREDIENT LIST

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. - trents replied to Ginger38's topic in Related Issues & Disorders
      1

      Shingles - Could It Be Related to Gluten/ Celiac

    2. - Ginger38 posted a topic in Related Issues & Disorders
      1

      Shingles - Could It Be Related to Gluten/ Celiac

    3. - Russ H commented on Scott Adams's article in Latest Research
      5

      Study Estimates the Costs of Delayed Celiac Disease Diagnosis (+Video)

    4. - Russ H posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      0

      Coeliac UK Research Conference 2025

    5. - Rejoicephd replied to Rejoicephd's topic in Related Issues & Disorders
      5

      Basic metabolic panel results - more flags


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,374
    • Most Online (within 30 mins)
      7,748

    Lynt
    Newest Member
    Lynt
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      I don't know of a connection. Lots of people who don't have celiac disease/gluten issues get shingles.
    • Ginger38
      I’m 43, just newly diagnosed with a horrible case of shingles last week . They are all over my face , around my eye, ear , all in my scalp. Lymph nodes are a mess. Ear is a mess. My eye is hurting and sensitive. Pain has been a 10/10+ daily. Taking Motrin and Tylenol around the clock. I AM MISERABLE. The pain is unrelenting. I just want to cry.   But Developing shingles has me a bit concerned about my immune system which also has me wondering about celiac and if there’s a connection to celiac / gluten and shingles; particularly since I haven't been 💯 gluten free because of all the confusing test results and doctors advice etc., is there a connection here? I’ve never had shingles and the gluten/ celiac  roller coaster has been ongoing for a while but I’ve had gluten off and on the last year bc of all the confusion  
    • Russ H
      There were some interesting talks, particularly Prof Ludvig Stollid's talk on therapeutics for coeliac disease.    https://www.youtube.com/playlist?list=PLRcl2mPE0WdigRtJPvylUJbkCx263KF_t
    • Rejoicephd
      Thank you @trents for letting me know you experience something similar thanks @knitty kitty for your response and resources.  I will be following up with my doctor about these results and I’ll read the articles you sent. Thanks - I really appreciate you all.
    • knitty kitty
      You're right, doctors usually only test Vitamin D and B12.  Both are really important, but they're not good indicators of deficiencies in the other B vitamins.  Our bodies are able to store Vitamin B12 and Vitamin D in the liver for up to a year or longer.  The other B vitamins can only be stored for much shorter periods of time.  Pyridoxine B 6 can be stored for several months, but the others only a month or two at the longest.  Thiamine stores can be depleted in as little as three days.  There's no correlation between B12 levels and the other B vitamins' levels.  Blood tests can't measure the amount of vitamins stored inside cells where they are used.  There's disagreement as to what optimal vitamin levels are.  The Recommended Daily Allowance is based on the minimum daily amount needed to prevent disease set back in the forties when people ate a totally different diet and gruesome experiments were done on people.  Folate  requirements had to be updated in the nineties after spina bifida increased and synthetic folic acid was mandated to be added to grain products.  Vitamin D requirements have been updated only in the past few years.   Doctors aren't required to take as many hours of nutritional education as in the past.  They're educated in learning institutions funded by pharmaceutical corporations.  Natural substances like vitamins can't be patented, so there's more money to be made prescribing pharmaceuticals than vitamins.   Also, look into the Autoimmune Protocol Diet, developed by Dr. Sarah Ballantyne, a Celiac herself.  Her book The Paleo Approach has been most helpful to me.  You're very welcome.  I'm glad I can help you around some stumbling blocks while on this journey.    Keep me posted on your progress!  Best wishes! P.S.  interesting reading: Thiamine, gastrointestinal beriberi and acetylcholine signaling https://pmc.ncbi.nlm.nih.gov/articles/PMC12014454/
×
×
  • 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.