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

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
      132,032
    • Most Online (within 30 mins)
      7,748

    CE1963
    Newest Member
    CE1963
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • Scott Adams
      Your experience is both shocking and critically important for the community to hear, underscoring the terrifying reality that cross-contamination can extend into the most unexpected and invasive medical devices. It is absolutely devastating that you had to endure six months of sickness and ultimately sustain permanent vision loss because a doctor dismissed your legitimate, life-altering condition. Your relentless research and advocacy, from discovering the gluten in MMA acrylic to finding a compassionate prosthodontist, is a testament to your strength in a system that often fails celiac patients. While the scientific and medical consensus is that gluten cannot be absorbed through the skin or eyes (as the molecules are too large to pass through these barriers), your story highlights a terrifying gray area: what about a substance *permanently implanted inside the body*, where it could potentially shed microparticles or cause a localized immune reaction? Your powerful warning about acrylic lenses and the drastic difference with the silicone alternative is invaluable information. Thank you for sharing your harrowing journey and the specific, severe neurological symptoms you endure; it is a stark reminder that celiac is a systemic disease, and your advocacy is undoubtedly saving others from similar trauma.
    • Scott Adams
      Those are driving distance from me--I will try to check them out, thanks for sharing!
    • Scott Adams
      I am so sorry you're going through this bad experience--it's difficult when your own lived reality of cause and effect is dismissed by the very professionals meant to help you. You are absolutely right—your violent physical reactions are not "what you think," but undeniable data points, and it's a form of medical gaslighting to be told otherwise, especially when you have a positive HLA-DQ2 gene and a clear clinical picture. Since your current "celiac specialist" is not addressing the core issue or your related conditions like SIBO and chronic fatigue, it may be time for a strategic pivot. Instead of trying to "reprove" your celiac disease to unwilling ears, consider seeking out a new gastroenterologist or functional medicine doctor, and frame the conversation around managing the complications of a confirmed gluten-free diet for celiac disease. Go in and say, "I have celiac disease, am strictly gluten-free, but I am still suffering from these specific complications: SIBO, chronic fatigue, dermatological issues, and high blood pressure linked to pain. I need a partner to help me address these related conditions." This shifts the focus from a debate about your diagnosis to a collaborative plan for your current suffering, which is the help you truly need and deserve to work toward bouncing back.
    • NanCel
      Hello, no I had to have them re done and then used a liner over the top.  Many dentists are not aware of the celiac effects.  Best of luck.   There is other material, yet, very expensive.
    • sleuth
      He is not just a psychiatrist.  He is also a neuroscientist.  And yes, I have already read those studies.   I agree with benfotiamine.  This is short term while glutened/inflammation occurs.  As I had already mentioned, these symptoms no longer exist when this phase passes.  And yes, I know that celiac is a disease of malnutrition.  We are working with a naturopath.
×
×
  • 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.