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

Glutened At "chili's Too" In Chicago O'hare Airport


zarfkitty

Recommended Posts

zarfkitty Explorer

I'm not all that angry but I'm definitely glutened. Ugh.

I used a restaurant card (I frankensteined a card to make it Gluten-free Casein-free) and spoke to the manager. The card talked about CC. Both the waitress and the manager were clearly annoyed as it was a busy night with quite a wait at the entrance.

I ordered the guilt-free chicken salad, which the manager said would be safe, but doesn't seem to be on any chili's gluten-free list on the internet now that I have access to the internet again.

I had a Gluten-free Casein-free peanut butter sandwich in my bag but I really wanted a dinner on a plate. I probably should have gone with my sandwich instead after seeing the attitude issues. And after I saw that they brought me ranch dressing (at least it was on the side) after reading my restaurant card, which clearly stated dairy products as not safe for me. It was an impulse buy and an impulse eat. :wacko:

I have another air travel trip next week but now I know to pack a nice picnic instead of negotiating an airport restaurant. :rolleyes:

Should I write a letter or would you just let this one go?


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



Celiac.com Sponsor (A8-M):



VegasCeliacBuckeye Collaborator

Do what you want, but understand this - gluten-free menus and products are off limits in my book at airports. The restaurant is smaller and the chances of CC is FREAKING HUGE! Even worse, some rules that places abide by in normal settings fly out the window at airport restaurants (McDonalds does not have dedicated fryers in some airports).

Don't eat there.

Prepare better next time (or just eat the PB & J you made with gluten-free bread).

buffettbride Enthusiast

You're very brave to even TRY eating at an airport. My daughter has Celiac and I haven't had to face that yet. The thought of anyone making her food but me scares me to no end!

I have had a positive experience at the Chili's in downtown denver. I looked at the web site before I ordered (to-go) the original ribs and corn on the cob for my daughter. It was one of her favorite meals pre-Celiac anyway so it was quite a treat for her to have something she knows she already loves.I also ordered at the very beginning of the day so it was not yet busy so it was easier to get someone's ear to listen and mitigate the possibility of CC.

I did follow-up with a letter via their web site thanking them for the positive experience. I figure any feedback we can give about the Celiac community, positive or negative, is great for the cause, although that was several days ago and I have not received a response.

Perhaps if you are a frequent traveler you can gain a rapport with restaurants in several airports that might be happier to accomodate you.

zansu Rookie

I got glutened at a Legal Seafood in Logan. It was several years ago, and I got a wonderful response back from management after I emailed them, but even Legal Seafood as an airport restaurant screws up...

I try not to eat in airports because of the crowds and the heavy emphasis on moving people through.

DarkIvy Explorer

I've been glutened at two regular Chili's in the past couple of months, so I would never bother with there airport junk. Seems rather horrifying to me.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      128,260
    • Most Online (within 30 mins)
      7,748

    Elizabeth Tageson
    Newest Member
    Elizabeth Tageson
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.1k
    • Total Posts
      70.8k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      Yes, I can imagine. My celiac journey started with a rejection of a blood donation by the Red Cross when I was 37 because of elevated liver enzymes. I wasn't a drinker and my family doctor checked me for hepatitis and I was not overweight. No answers. I thought no more about it until six years later when I landed a job in a healthcare setting where I got annual CMP screenings as part of my benefits. The liver enzymes were continually elevated and creeping up every year, though they were never super high. My primary care doc had no clue. I got really worried as your liver is pretty important. I finally made an appointment with a GI doc myself and the first thing he did was test me for celiac disease. I was positive. That was in about 1996. After going on a gluten-free diet for three months the liver enzymes were back in normal range. Another lab that had gotten out of whack that has not returned to normal is albumin/total protein which are always a little on the low side. I don't know what that's about, if it's related to the liver or something else like leaky gut syndrome. But my doctors don't seem to be worried about it. One thing to realize is that celiac disease can onset at any stage of life. There is a genetic component but there is also an epigenetic component. That is, the genetic component is not deterministic. It only provides the potential. There needs also to be some health or environmental stressor to activate the latent gene potential. About 40% of the population have the genetic potential to develop celiac disease but only about 1% actually do.
    • cristiana
      Hello @Heather Hill You are most welcome.  As a longstanding member and now mod of the forum, I am ashamed to say I find numbers and figures very confusing, so I rarely stray into the realms of explaining markers. (I've self-diagnosed myself with dyscalculia!)  So I will leave that to @Scott Adams or another person. However as a British person myself I quite understand that the process with the NHS can take rather a long time.  But just as you made a concerted effort to eat gluten before your blood test, I'd advise doing the same with eating gluten before a biopsy, in order to show if you are reacting to gluten.  It might be worth contacting the hospital or your GPs secretary to find out if they know what the current waiting time is. Here is a page from Coeliac UK about the current NHS recommendations. https://www.coeliac.org.uk/information-and-support/coeliac-disease/getting-diagnosed/blood-tests-and-biospy/#:~:text=If you remove or reduce,least six weeks before testing. Cristiana  
    • MI-Hoosier
      Thanks again. My mom was diagnosed over 50 years ago with celiac so grew up watching her deal with the challenges of food. I have been tested a few times prior due to this but these results have me a bit stunned. I have a liver disease that has advanced rapidly with no symptoms and an allergy that could be a contributing factor that had no symptoms. I guess I’ll call it lucky my Dr ordered a rescreen of a liver ultrasound from 5 years ago that triggered this or I would likely have tripped into cirrhosis. It’s all pretty jarring.
    • Heather Hill
      Many thanks for your responses, much appreciated.  The tests did include tTg IgA and all the other markers mentioned.  I also had sufficient total IgA so if I'm reading the Mayo clinic thing correctly, I didn't really need the anti-deaminated gliadin marker? So, if I am reading the information correctly do I conclude that as all the other markers including tTg IgA and DGP IgG and tTg IgG and EMA IgA are all negative, then the positive result for the immune response to gliadin, on it's own, is more likely to suggest some other problem in the gut rather than Coeliac disease? Until I have a view from the medics (NHS UK) then I think I will concentrate on trying to lower chronic inflammation and mend leaky gut, using L glutamine and maybe collagen powder. Thank you for your help so far.  I will get back in touch once I have a response, which sadly can take quite a long time.   Kindest Heather Hill 
    • trents
      To put this in perspective, most recent pretest "gluten challenge" guidelines for those having already been eating reduced gluten or gluten free for a significant time period is the daily consumption of 10g of gluten (about the amount in 4-6 slices of wheat bread) for a minimum of two weeks leading up to the day of testing (antibody or biopsy). And I would certainly give it more than two weeks to ensure a valid test experience. Short answer: If it were me, yes, I would assume I have celiac disease and launch full bore into gluten-free eating. I think the tTG-IGA is reliable enough and your score is solid enough to make that a reasonable conclusion. Here is an article to help you get off to a good start. It's easy to achieve a reduced gluten free state but much more difficult to achieve consistency in truly gluten-free eating. Gluten is hidden in so many ways and found in so many food products where you would never expect to find it. For example, soy sauce and canned tomato soup (most canned soups, actually), pills, medications, health supplements. It can be disguised in terminology. And then there is the whole issue of cross contamination where foods that are naturally gluten free become contaminated with gluten incidentally in agricultural activities and manufacturing processes: Eating out at restaurants is a mine field for those with celiac disease because you don't know how food is handled back in the kitchen. Gluten free noodles boiled in the same water that was used for wheat noodles, eggs cooked on the same griddle that French toast was, etc.  
×
×
  • Create New...