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

How Do You Deal With Eating Out?


Mommy2Ellie

Recommended Posts

Mommy2Ellie Rookie

Just curious how to deal with this? We eat out about twice a month, or whenever we go to the nearest city, which is about two hours away. I don't know how to order food for Ellie! All of their baby plates or kids meals have gluten. Any advice is GREATLY appreciated!!!


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



Celiac.com Sponsor (A8-M):



Mtndog Collaborator

Wanted to say welcome first!

Many big chain restaurants like Bone Fish, Legal Seafoods, Not Your Average Joe's, The Outback have gluten free menus. If you call ahead, you can ask if they've dealt with gluten-free before.

I usually write down what I can't have and then ask them what they recommend. Another option is to get the Triumph Dining Cards or make your own. I list most common things like flour, bread, pasta, breadcrumbs, malt vinegar, etc.

The good news is that in the last 3 years- places have become MUCH more aware!

Rondar2001 Apprentice

We eat out a couple of times a month and so far have been very lucky. Before we go, I try to research a possible restaraunt and check their website to see if they have any allergy information. I also check with our local celiac chapter's website for suggestions of gluten free friendly places. We also discuss the importance of gluten free with the server when we order and have found most places to be pretty knowledgable.

My biggest complaint is that the gluten free options tend to be in adult portions instead of kids meals. If they can't accomodate the smaller portion, she just brings home a doggy bag (although this tends to up the cost quite a bit).

ShayFL Enthusiast

I have found calling ahead to be invaluable. Try to talk to the head manager or the head chef. Tell them it will be 2 adults and one child eating and the child needs gluten-free food. Could they prepare something just for her so that your family can enjoy and frequent their restaurant. The economy isnt great right now and restaurants need our business. You might find that they are more than willing to accommodate you.

missy'smom Collaborator
We eat out a couple of times a month and so far have been very lucky. Before we go, I try to research a possible restaraunt and check their website to see if they have any allergy information. I also check with our local celiac chapter's website for suggestions of gluten free friendly places. We also discuss the importance of gluten free with the server when we order and have found most places to be pretty knowledgable.

Good advice. I do the same when we go out of town. I'll add that I have checked to see if the place I'm traveling to has a Celiac Support Group and contacted them for info on local options. I have also mapquested a town and clicked on restaurants for a list and through a process of elimination picked a couple that had webites with menus(they happened to not be large chains but local family owned and small chain) and e-mailed them for info concerning a few dishes that I thought might work. I also print out gluten-free menus and allergy info pages from the large chain websites and put them in a presentation pholio with clear verticle pocket pages and carry it in the car with me. Don't be afraid to make up and order your own dishes that are not on the menu, as long as they are simple and use the ingedients that that restauraunt is likely to have, they will usually accomodate. I order one meal at a restaurant that used to be on the menu but is no longer, however they still use the ingredients, so will make it that way. Another place I've ordered something that is not on the menu but I make up from the list of ingredients that is on the website's extensive allergy info page.

wsieving Contributor

I am so glad you asked that question!! I have been wondering this myself, and you all have great suggestions!!

Tristan's Mama Newbie

My girlfriend who is a member here, who's son has Celiac Disease, actually answered this question for me today! She said there are restaurants who do offer Gluten free items, and for the ones that don't she brings a separate meal for her son. She said there was a place online, and some stores, where you can purchase gluten-free ready to go meals. She just brings them and a microwave container, and has them heat up her son's meal. She has yet to have any difficulties doing this. She also advised me of the fact that McDonald's french fries contain gluten, but that Burger King does not. I called both in our area to confirm this today, and they informed me of the same. Which for us is a God send...as Tristan is obsessed with french fries!


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



Celiac.com Sponsor (A8-M):



NewGFMom Contributor

We tend to go to Thai and Japanese restaurants where we can get Mr. Picky-ness a bowl of rice pasta. He likes to squeeze lemon juice on it.

At a lot of places, hot dogs and french fries are a pretty safe bet, if you call first and make sure they understand about cross contamination.

Otherwise, we pack a meal for him and order him a fancy drink or something. If the city near you is medium sized, you may be surprised by the options. We found a ton of gluten free food in Bemidji, Minnesota and all over rural New Hampshire when we specifically looked for it.

Good luck!

happygirl Collaborator

These cards may help: Open Original Shared Link

Always speak with a manager or chef - don't rely on the waitress.

Make sure you cover 1. the ingredients in the food and 2. the preparation of the food (clean utensils, pan, etc).

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,061
    • Most Online (within 30 mins)
      7,748

    420jen
    Newest Member
    420jen
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):




  • Who's Online (See full list)


  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      Maybe celiac but maybe NCGS that was misdiagnosed as IBS morphing gradually into celiac. Is NCGS a new category to you? It shares many of the same GI symptoms with celiac disease but does not damage the small bowel lining like celiac.
    • knitty kitty
      Thiamine has antifungal properties.  The body uses thiamine to keep bacteria and yeasts from overgrowth in the digestive system.   Fluconazole use can cause thiamine deficiency.   Supplementing with thiamine in the form Benfotiamine would be beneficial as Benfotiamine promotes intestinal healing.   Thiamine and the other B vitamins tend to be low in Celiac due to malabsorption.  Talk to your doctor about supplementing vitamins and minerals.
    • Scott Adams
      Welcome @Natalia Revelo, your experience is profoundly difficult and, sadly, not entirely unique within the celiac community. It's the frustrating reality of "silent" or ongoing damage that isn't captured by the MARSH score alone, which only measures active villous atrophy. Your normal biopsy suggests your diet is preventing the classic autoimmune attack, but it doesn't mean your gut has fully healed or that other issues aren't at play. The inflammation from your newly discovered milk and egg allergies is a huge clue; this constant allergic response can create a low-grade inflammatory environment that severely hampers nutrient absorption, effectively creating a "leaky gut" scenario independent of celiac damage. This is likely why your iron stores deplete so rapidly—your body is both unable to absorb it efficiently and may be losing it through inflammation. While the functional medicine path is expensive, it's clearly providing answers and relief that traditional gastroenterology, focused solely on the gluten-free diet and biopsy results, is missing. To move forward, continue the gut-healing protocols your functional doctor recommends (perhaps exploring alternative options to glutamine that won't irritate your cystitis), maintain your strict avoidance of all allergens and irritants, and know that true healing is a multi-faceted process. You might seek a second opinion from a different gastroenterologist who is more knowledgeable about non-responsive celiac disease and the complex interplay of food allergies and micronutrient absorption, but your current path, while costly, seems to be leading you toward the steady health you need.
    • knitty kitty
      Have you had a DNA test to look for Celiac disease genes?  If she doesn't have any celiac specific genes, look for another explanation.  If she does have Celiac genes, assume they are turned on and active Celiac disease is progressing.  All first degree relatives (mother, father, siblings, children) should be genetically tested as well.   Sometimes blood tests are ambiguous or false negatives if one has anemia, diabetes or thiamine deficiency.  Certain medications like antihistamines and steroids can suppress the immune system and result in false negatives or ambiguous results on antibody tests.  
    • Heatherisle
      That was just the visual report, so need to wait for confirmation or otherwise from the results. They did take a biopsy from the upper end of the duodenum(D1). D2 looked unremarkable on the camera. Just wish we didn’t have to wait so long for the results as she’s naturally a very anxious person. But thanks so much for taking the time to answer me
×
×
  • Create New...