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

Conference Travel?


kittty

Recommended Posts

kittty Contributor

Does anyone here have to travel to conferences for work? Next month is the first conference since I went gluten free, and I'm already having nightmares.

Food for the conference consists of:

Breakfast: breakfast bar in the hotel, with waffles, toast, pastries, fruit

Snacks: cookies and danishes

Lunch: A choice of pasta with meat, or pasta without meat (at least they took the veggies into consideration)

Dinner: Roast in gravy, creamed corn, seasoned potatoes, buttery biscuits, and apple crisp

Gluten! Nothing but gluten!

Other than stealing all the apples from the breakfast bar, what do I do? Should I take a cooler of food for myself, or live on Larabars for a couple of days?

I'd be very interested to know how others overcome situations like this.


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



Celiac.com Sponsor (A8-M):



Persei V. Enthusiast

I sort of kind of snuck an eletric stove inside the apartments of the hotels I travel to. And then I live of Coke, tapioca and Chocosoy (a brand of gluten and lactose free chocolate, which tastes absolutely normal). I also make my own coffee. Hmm, coffee...

Anyhow, take your own food, surely! If there's barely nothing you can eat, they have to understand the need of bringing your own meals and stuff. Otherwise, just make sure you puke on their favorite shoes :P

bartfull Rising Star

Take your own food. If there is a place to heat things, great. If not, take something you don't mind eating cold. Sandwiches on gluten-free bread, gluten-free pasta salads, whatever you like. There's no need to starve yourself. You can even take some gluten-free desserts. If you pack the cooler with pre-frozen bottled water you'll even have something to drink. Those bottles will sweat though, so make sure you have some kind of netting above the ice bottles to keep your food elevated.

IrishHeart Veteran

Please, read this thread? Maybe it will help. It does not have to be that difficult, I promise you. ;) Karen has done a lot of work finding all these great ideas ...and a travel cooler helps a lot.

  • 1 month later...
user853 Apprentice

I have asked the "waiters" at these events for a special meal (lunch and dinners) and have always been given something. This is when I was just vegetarian and not gluten-free.

I travel a lot a s bring a ton of food. For breakfast I usually heat up a cereal of quinoa flakes and add freeze dried strawberries. Plus fruit from the grocery and nuts.

Lots of soup heated up in the microwave.

I always have 1 or 2 gluten-free Go Picnic boxes with me too. Normally don't eat processed foods, but sometimes it is the only notion.

1desperateladysaved Proficient

Does anyone here have to travel to conferences for work? Next month is the first conference since I went gluten free, and I'm already having nightmares.

Food for the conference consists of:

Breakfast: breakfast bar in the hotel, with waffles, toast, pastries, fruit

Snacks: cookies and danishes

Lunch: A choice of pasta with meat, or pasta without meat (at least they took the veggies into consideration)

Dinner: Roast in gravy, creamed corn, seasoned potatoes, buttery biscuits, and apple crisp

Gluten! Nothing but gluten!

Other than stealing all the apples from the breakfast bar, what do I do? Should I take a cooler of food for myself, or live on Larabars for a couple of days?

I'd be very interested to know how others overcome situations like this.

I take so much food with on my trips that I come home with less stuff then I left with. I am a committed believer in eating my own food. I use an electric skillet or crock pot at the hotel. I sometimes precook food. I sometimes back in convenient packs. That means the meat, spices, and veggies I need to make the dish.

I hope you will have a healthy and safe trip.

Diana

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 Scott Adams's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      46

      Supplements for those Diagnosed with Celiac Disease

    2. - trents replied to Woodster991's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      10

      Is it gluten?

    3. - RMJ replied to wellthatsfun's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      3

      nothing has changed

    4. - asaT replied to wellthatsfun's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      3

      nothing has changed

    5. - nanny marley replied to SilkieFairy's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      IBS-D vs Celiac

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

    • Total Members
      133,342
    • Most Online (within 30 mins)
      7,748

    Muhammad
    Newest Member
    Muhammad
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • trents
      You may also need to supplement with B12 as this vitamin is also involved in iron assimilation and is often deficient in long-term undiagnosed celiac disease.
    • trents
      @par18, no, Scott's use of the term "false negative" is intentional and appropriate. The "total IGA" test is not a test used to diagnose celiac disease per se. The IGA immune spectrum response encompasses more than just celiac disease. So, "total IGA" refers to the whole pie, not just the celiac response part of it. But if the whole pie is deficient, the spectrum of components making it up will likely be also, including the celiac disease response spectrum. In other words, IGA deficiency may produce a tTG-IGA score that is negative that might have been positive had there not been IGA deficiency. So, the tTG-IGA negative score may be "false", i.e, inaccurate, aka, not to be trusted.
    • RMJ
      This may be the problem. Every time you eat gluten it is like giving a booster shot to your immune system, telling it to react and produce antibodies again.
    • asaT
      Scott, I am mostly asymptomatic. I was diagnosed based on high antibodies, low ferritin (3) and low vitamin D (10). I wasn't able to get in for the biopsy until 3 months after the blood test came back. I was supposed to keep eating gluten during this time. Well why would I continue doing something that I know to be harmful for 3 more months to just get this test? So I did quit gluten and had the biopsy. It was negative for celiacs. I continued gluten free with iron supps and my ferritin came back up to a reasonable, but not great level of around 30-35.  Could there be something else going on? Is there any reason why my antibodies would be high (>80) with a negative biopsy? could me intestines have healed that quickly (3 months)?  I'm having a hard time staying gluten free because I am asymptomatic and i'm wondering about that biopsy. I do have the celiacs gene, and all of the antibody tests have always come back high. I recently had them tested again. Still very high. I am gluten free mostly, but not totally. I will occasionally eat something with gluten, but try to keep to a minimum. It's really hard when the immediate consequences are nil.  with high antibodies, the gene, but a negative biopsy (after 3 months strict gluten-free), do i really have celiacs? please say no. lol. i think i know the answer.  Asa
    • nanny marley
      I have had a long year of testing unfortunately still not diagnosed , although one thing they definitely agree I'm gluten intolerant, the thing for me I have severe back troubles they wouldnt perform the tests and I couldn't have a full MRI because I'm allergic to the solution , we tryed believe me  I tryed lol , another was to have another blood test after consuming gluten but it makes me so bad I tryed it for only a week, and because I have a trapped sciatic nerve when I get bad bowels it sets that off terribly so I just take it on myself now , I eat a gluten free diet , I'm the best I've ever been , and if I slip I know it so for me i have my own diagnosis  and I act accordingly, sometimes it's not so straight forward for some of us , for the first time in years I can plan to go out , and I have been absorbing my food better , running to the toilet has become occasionally now instead of all the time , i hope you find a solution 🤗
×
×
  • 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.