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

Dealing With Special Events/catered Events


june bug

Recommended Posts

june bug Newbie

Hi all!

I was only diagnosed with celiac 6 months ago, so I am still sort of new to this. The sad goodbye to my favorite foods is not so bad. I am a good cook and am able to work around the gluten at home quite easily. MY question for everyone is: What do you do when you must attend special events or catered functions. My approach, until now, has been to avoid them and just not attend. I have several events coming up, though, that I must attend, and I am unsure how to handle the "food part". One function in particular is a charity event. Black tie with a sit down dinner. We are sitting with the honoree and I can't do my trusty "slip to the bathroom and eat a protein bar and then leave my food untouched thing" What would you all do?????

This is the thing I hate most...being different, or an inconvenience.

Any suggestions are greatly appreciated.

June bug


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



Celiac.com Sponsor (A8-M):



Skylark Collaborator

At events where I have to eat, like conferences, I contact the organizer ahead of time and politely ask about gluten-free food. I've always been accommodated with very little fuss. People who run dinner events are accustomed to vegetarians and people with allergies, and I find a lot of them are getting very used to celiacs as well. As you know, it's really easy for a chef to work around gluten.

ChristieKate Rookie

I had my first post-diagnosis black tie event just this past Monday. As it was for my husband's work (not mine) he called the caterer and spoke to their executive chef and explained my "special needs" right when he RSVP'd. They said no problem - they're used to accommodating gluten-free and allergies. At the event, I did accidentally get the regular dinner served, but as soon as I mentioned it the head waitress (I don't know the proper title) came over, apologized discretely and brought my proper meal. Same with all courses - no problem. I had a delicious dinner and nobody at the table even mentioned it (which was also a great part!).

Lisa Mentor

I would eat before hand. Do not arrive hungry and don't worry about the catered event. If, by chance, you see steamed shrimp or crab claws, a cheese assortment or various non-gluten display - all the better.

I don't bother the catering team. They are too busy and hired by someone other than ME.

Generally, at these events, I talk too much to eat - so I don't miss much. :blink: I do enjoy the wine that's offered. :P

A must attend sit down event... I would contact the caterer and state your dietary issues. Find some options to the offered menu..just meat, just veggies, just salads. And an extra gratuity is always appreciated if known in advance, for that extra service. ;)

ryebaby0 Enthusiast

Like the others, we've contacted the caterer or event organizer, and if we give them specific brands or specific directions, they can usually provide something. High-end events are even more likely to be able to accomodate. My husband does always eat before he goes, however, just in case something goes wrong.

Remember -- every time we ask for gluten-free food, or peanut-free, or whatever, the caterer/planner gets a reminder that we are out here! Remember when vegetarian selections were "weird"? Progress is made one plate at a time

  • 2 weeks later...
LynnJ Newbie

Similar to previous responses, I contact the organizer of the event to let them know that I am gluten-intolerant, and they have always been very accommodating. My family, as well as my husband's family also are aware of my special dietary needs, and have many gluten-free dishes available at holiday and other family gatherings. I've been very fortunate.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,202
    • Most Online (within 30 mins)
      7,748

    PatBurnham
    Newest Member
    PatBurnham
    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
      NCGS does not cause damage to the small bowel villi so, if indeed you were not skimping on gluten when you had the antibody blood testing done, it is likely you have celiac disease.
    • Scott Adams
      I will assume you did the gluten challenge properly and were eating a lot of gluten daily for 6-8 weeks before your test, but if not, that could be the issue. You can still have celiac disease with negative blood test results, although it's not as common:  Clinical and genetic profile of patients with seronegative coeliac disease: the natural history and response to gluten-free diet: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5606118/  Seronegative Celiac Disease - A Challenging Case: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9441776/  Enteropathies with villous atrophy but negative coeliac serology in adults: current issues: https://pubmed.ncbi.nlm.nih.gov/34764141/  Approximately 10x more people have non-celiac gluten sensitivity than have celiac disease, but there isn’t yet a test for NCGS. If your symptoms go away on a gluten-free diet it would likely signal NCGS.
    • Xravith
      I'm very confused... My blood test came out negative, I checked all antibodies. I suppose my Total IgA levels are normal (132 mg/dl), so the test should be reliable. Still, I'm not relieved as I can't tolerate even a single biscuit. I need to talk to my doctor about whether a duodenal biopsy is necessary. But it is really possible to have intestinal damage despite having a seronegative results? I have really strong symptoms, and I don't want to keep skipping university lectures or being bedridden at home.
    • Scott Adams
      They may want to also eliminate other possible causes for your symptoms/issues and are doing additional tests.  Here is info about blood tests for celiac disease--if positive an endoscopy where biopsies of your intestinal villi are taken to confirm is the typical follow up.    
    • Scott Adams
      In the Europe the new protocol for making a celiac disease diagnosis in children is if their tTg-IgA (tissue transglutaminase IgA) levels are 10 times or above the positive level for celiac disease--and you are above that level. According to the latest research, if the blood test results are at certain high levels that range between 5-10 times the reference range for a positive celiac disease diagnosis, it may not be necessary to confirm the results using an endoscopy/biopsy: Blood Test Alone Can Diagnose Celiac Disease in Most Children and Adults TGA-IgA at or Above Five Times Normal Limit in Kids Indicates Celiac Disease in Nearly All Cases No More Biopsies to Diagnose Celiac Disease in Children! May I ask why you've had so many past tTg-IgA tests done, and many of them seem to have been done 3 times during short time intervals?    
×
×
  • 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.