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

Restaurants


Minette

Recommended Posts

Minette Contributor

I'm confused by what seems like a more relaxed standard for restaurants than for our own home kitchens. I keep reading that to make your kitchen gluten-free, you need to replace all your plastic/wooden items and nonstick pans, rigidly segregate all gluten-containing foods, etc.

I'm not an expert in restaurant kitchens, but I'd assume that even those that have a gluten-free menu don't meet this standard (unless the entire restaurant is gluten-free). Even if the utensils, pots, and countertops are clean and the cooks wash their hands regularly, there are probably still trace amounts of gluten everywhere. So why is it considered generally safe?

I'm just trying to get a handle on what we can & can't expect to do with our celiac kid -- assuming we can get her to eat something gluten-free (i.e., not grilled cheese) in a restaurant in the first place.


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



Celiac.com Sponsor (A8-M):



Mom2J112903 Newbie

I personally feel you have to make that choice for yourself and your family based on how much, if any gluten that a person can be in contact with/digest. For example my son actually has to eat the gluten to become symptomatic. So we do not worry about personal care products with him. He is tube fed now so no worries about cross contimanation now. Before though, we had dedicated "little man" pots, pans, etc. I would scrub the counters if I had gluten filled things on them before preparing little man's. Never had a problem with him but others would have to go to a gluten free house. We were able to take him out to eat at certain places without an issue, Chilli's was WONDERFUL! Outback is supposed to be a good place as well. What we started doing though is packing his own food, that way we knew exactly what he was getting and not having to worry.

psawyer Proficient

There are many of us here who do not have dedicated gluten-free households, although I am no longer one of them. We had a mixed kitchen for years. Even though we do not intentionally bring any gluten into our home, there is always a risk of accidental contamination.

Thorough washing of utensils is sufficient for most of us. Restaurants such as Outback are aware, and ensure that only fresh, clean implements are used in preparation of gluten-free orders.

Yes, there will be trace amounts of gluten in the kitchen. There is a risk. The level of risk varies from establishment to establishment.

I am careful--I am not paranoid.

kareng Grand Master

Some thoughts:

If they have never gotten an order right pre- gluten-free, how would you expect them to get it right now? (Appleby's is an example for me)

Are they very busy ?

Do they have a lot of teens or a high turn- over of wait staff & kitchen staff? ( never see the same waiter twice or always has a help wanted sign, etc)

Is most of the food naturally gluten-free? Like Bonefish Grill or a Persian restauraunt that uses little to no flour other than bread. A place that never puts croutons on salads.

Do they have regular procedures that keep the gluten stuff apart from the non- gluten. For example, Five Guys only fries potatoes nothing else.

Do they have trained chefs rather than $9 an hour cooks?

You don't need each of these before eating there. For example, if they have a teenager who only fixes salads during lunch rush but has no gluten ingredients for her to mess up and add, it's probably OK.

Skylark Collaborator

You eat every single meal in your kitchen. You only eat sometimes in a restaurant.

Sesara Rookie

As a former restaurant chef, while I would say that there's no 100%, if you talk to the chef, and they have a decent understanding of the issues of Celiac and gluten free, you might be able to trust things.

In my former non-SAHM life, I had a number of regulars at my restaurant who were gluten free, a few who were celiac, and I totally respected their issue and was always honest when I couldn't guarantee that something would be gluten-free. Wood cutting boards are not allowed in restaurant kitchens, btw, only plastic ones, though I know that's not perfect. Utensils are usually metal or silicone because they're more durable. And pans are usually stainless steel for similar reasons - nonstick would be ruined in no time flat. Also, most restaurants prepare glutened foods, like cake, at a different station than the line where most dishes are prepared for service, which cuts down on cross contamination on the line.

Really, the biggest danger in restaurants for a knowledgeable chef, from what I can see, is convenience foods. If a chef doesn't truly know what's in their food, they can't guarantee that it's safe. At my restaurant, I made almost everything completely from scratch, so while I was honest that my kitchen was not gluten free, I always did my best to keep gluten-free foods on non-contaminated, clean surfaces, and could generally tell people which products did not contain gluten. There were a few products that I wasn't sure about and those I would offer to show the labels on, but I could pretty well guarantee that, for instance, my salmon or steak or chicken, often their sauce, and their sides were all gluten free.

So find a small restaurant and talk to the chef and find someone you can trust to work with you, that's my best advice.

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

      Newly diagnosed mam to coeliac 11 year old

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

      Celiac support is hard to find

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

      Help understand results

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

      Help understand results

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

      Newly diagnosed mam to coeliac 11 year old

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

    • Total Members
      132,958
    • Most Online (within 30 mins)
      7,748

    DLA
    Newest Member
    DLA
    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

    • cristiana
      You are very welcome @Dizzyma. Gastroenterologists are now following this rule in the UK more and more with children, so I am not surprised your daughter is not having an endoscopy.   Switching to a gluten free diet should begin to help, but also, even if you have to have testing done privately, it would be very helpful for you to find out if your daughter has vitamin and mineral deficiencies, which is highly likely,    In the UK tests are generally offered on the NHS for B12 and ferritin, and sometimes vitamin D.  Shortages in these can really cause any anxiety or depression or ramp it up. If you do end up supplementing, make sure your GP is aware as levels do need to be monitored, for example,  too much ferritin can cause huge health issues. Re: anxiety, definitely speak to a GP or another health care professional about this if it is an issue. Hopefully the Coeliac Society of Ireland will also be able to help. Cristiana  
    • 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   
×
×
  • 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.