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

Eating Out With Kids...gluten Foods At The Same Table


stolly

Recommended Posts

stolly Collaborator

For non-celiac parents of celiac kids, how do you avoid CC from your own food when eating out? For example, if you're eating a hamburger or a roll or something, and your toddler needs help with his/her food or needs hands wiped? At home it's easy, we just get up and wash our hands several times during the meal if/when we eat things with gluten at the same table as our daughter. (2.5 yrs old). I figure it's trickier when eating out...are wipes enough to clean the gluten off our hands? Any tips/suggestions for keeping her safe when we eat out? Thanks!


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



Celiac.com Sponsor (A8-M):



gfgypsyqueen Enthusiast

I guess my family handles thigns differently than some. I have Celiacs. My spouse does not. One kid has severe food allergy. Other kid (3 yr old) has Celiac, dairy allergy, and other allergies being tested.

We go through tons of silverware, cutting boards, and plates in the day. When we go out to eat, each person has their own silverware and ONLY that silverware is used on that plate and the food on that plate. I mean most of the meals the Celiac child eats do not involve her picking them up like a sandwich. If needed, get an extra fork and knife that you can touch with wiped (gluteny) hands and cut the food more etc. I have not purposefully touched wheat in years. But my husband eats gluteny stuff when we eat out. We just wipe our hands off (wipes) well if we are touching somethign the kids can't have to eat.

We get extra napkins when eating out. The kids tend to drop theirs or crumble it up into a ball that is unusable....When they need cleaned up, it is their napkin or a new napkin. Or wipes if it is a really big mess.

There is no touching of plates or sharing of glasses especially between the kids. At home, the kids generally sit in the same spot at the table. And they are only allowed to eat at the table (keep those crumbs in one place :rolleyes: )

I guess they have gotten used to the rules because it is second nature now. Sounds a bit crazy, but it works for us.

HAK1031 Enthusiast

You could cut everything up, etc. for your kids before you start eating. The wipes are also a good idea. I am the celiac in my family, but if I had a kid with celiac, I don't think I would purposefully order gluteny foods in restaurants with the kids. I mean, I might not check on the sauce and I wouldn't give the waiter the whole run-down on CC, but I wouldn't order spaghetti or a sandwich or something that could make crumbs or get everywhere. If I wanted to get gluteny foods I would do it on a night when the kids weren't with me.

dandelionmom Enthusiast

Since I have celiac disease too, I just take charge of that daughter's plate. But when I eat out alone with my girls and I have to help with one of the gluten plates, I just try to prep it as well as possible, then wipe my hands really really really well on a few baby wipes.

It helps to try to order something they won't need much help with and something that I don't have to touch much.

JennyC Enthusiast

When I eat out with my son I try to order gluten free food as well, so I don't have to worry about it. It just seems much easier.

Owen'sMom Rookie

I also order gluten free foods when I'm out with my son. Especially since he doesn't eat that much yet anyways and it wouldn't be worth ordering a meal for him, so I just share with him. But I will later also still order gluten free just so I don't have to worry about anything gluteny touching his plate/food.

Juliebove Rising Star

My daughter is 9 so she needs less help from me than she used to.

If she needs to have her food cut up, I cut it up first. Actually now that I think about it, my food tends to be gluten free as well. I am allergic to eggs and dairy and that pretty much lets out most bread products. There is one place that makes its bread from scatch and it is safe for me to eat. When I eat this, I eat it with hummus. My daughter loves hummus so I just order a plate of it for her with cucumber slices on it rather than bread.

One place that is a concern is the Old Spaghetti Factory. Although it is nice that they have a gluten-free menu, they also have regular bread and there are crumbs and chunks of it everywhere! I'm a little surprised the health dept. has not taken a good look at their booths! Also they tend to slap that loaf of bread on the table before you can say, "No bread!" I once got a flying crumb of it in my mouth as my dad was cutting it. Grrr...

We also have problems when my husband dines with us because he doesn't understand our food allergies (daughter is allergic to wheat and gluten, rather than celiac), and often tries to force her to eat food from his plate. He has also grabbed food from her plate while he has her allergens on his hands. When he does this, she just pushes her plate to him and says, "It's yours now!"

Tonight we will be going for Mexican food and I can bet you dollars to donuts he will proudly order flour tortillas. I don't think he even likes the flour ones better but he thinks it's a great thing that he has no food allergies and it's sort of like he is boasting. "Look at me! I can eat this and YOU can't!" Luckily the place we are going to knows what my daughter and I order. If we get a certain couple of wait people they just say, "You want what you always have?" They fix the food special for us. My husband does not normally dine with us if we can help it. Hehehehe. Just a lot easier that way. We have had problems at other Mexican places though when they combine the flour and corn tortillas in the same server. Then we either ask for more corn ones in a separate server or just do without.

Most of the time I try to order the same thing that my daughter is ordering, even though my allergies are not as extensive as hers. Somehow I think it makes her feel better to know we are eating the same thing. I let her order the adult meal if that is what she wants because her choices are often limited to non-existant on the kid's menu. Or we order all side dishes.


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



Celiac.com Sponsor (A8-M):



Tori's Dad Apprentice

For the most part we simply don't eat out. The anxiety is not worth the not having to wash dishes. On the 5-6 occasions we do eat out, my wife is also Celiac so she and my daughter sit on one side of the booth and my son and I sit on the other.

QuiteaPair Newbie
My daughter is 9 so she needs less help from me than she used to.

If she needs to have her food cut up, I cut it up first. Actually now that I think about it, my food tends to be gluten free as well. I am allergic to eggs and dairy and that pretty much lets out most bread products. There is one place that makes its bread from scatch and it is safe for me to eat. When I eat this, I eat it with hummus. My daughter loves hummus so I just order a plate of it for her with cucumber slices on it rather than bread.

One place that is a concern is the Old Spaghetti Factory. Although it is nice that they have a gluten-free menu, they also have regular bread and there are crumbs and chunks of it everywhere! I'm a little surprised the health dept. has not taken a good look at their booths! Also they tend to slap that loaf of bread on the table before you can say, "No bread!" I once got a flying crumb of it in my mouth as my dad was cutting it. Grrr...

We also have problems when my husband dines with us because he doesn't understand our food allergies (daughter is allergic to wheat and gluten, rather than celiac), and often tries to force her to eat food from his plate. He has also grabbed food from her plate while he has her allergens on his hands. When he does this, she just pushes her plate to him and says, "It's yours now!"

Tonight we will be going for Mexican food and I can bet you dollars to donuts he will proudly order flour tortillas. I don't think he even likes the flour ones better but he thinks it's a great thing that he has no food allergies and it's sort of like he is boasting. "Look at me! I can eat this and YOU can't!" Luckily the place we are going to knows what my daughter and I order. If we get a certain couple of wait people they just say, "You want what you always have?" They fix the food special for us. My husband does not normally dine with us if we can help it. Hehehehe. Just a lot easier that way. We have had problems at other Mexican places though when they combine the flour and corn tortillas in the same server. Then we either ask for more corn ones in a separate server or just do without.

Most of the time I try to order the same thing that my daughter is ordering, even though my allergies are not as extensive as hers. Somehow I think it makes her feel better to know we are eating the same thing. I let her order the adult meal if that is what she wants because her choices are often limited to non-existant on the kid's menu. Or we order all side dishes.

QuiteaPair Newbie

I have three children, 5-7 & 9 year the 9 year old boy has celiacs as do I, but no-one else in my family does. We went all didn't go Gluten free at first, but one incidence at a restaurant when my son just broke down as his Dad and sisters enjoyed freshly baked cinnamon rolls. That was it for the rest of the family. My husband now understands how important we all stand up for eachother. My son is still having reactions, loose stools, but we aren't sure where he is getting the reaction from? All gluten-free food, however, we haven't replaced cookware. Does anyone know if the gluten stays on after washing everything?

I hope you and your daughter win the battle with your husband. It is paramount for her recovery and your sanity that he makes more of an effort to support her gluten-free life. Good luck.

cyberprof Enthusiast
My son is still having reactions, loose stools, but we aren't sure where he is getting the reaction from? All gluten-free food, however, we haven't replaced cookware. Does anyone know if the gluten stays on after washing everything?

Good luck.

I'm sure others will answer, but yes you should replace any cookware (which previously was used with gluten) that is not 1) stainless steel with no cracks, ridges or hard to clean areas or 2) glass, china or uncracked bakeware.

This means replace wooden spoons and cutting boards, plastic cutting boards, spatulas, colanders and strainers (I got glutened from gluten-free pasta drained in an old colander), tupperware and serving dishes that are plastic or wood, non-stick cookware, waffle irons, toasters, etc. All of this stuff harbors gluten and to my understanding cannot be removed by washing, sanitizing etc. It's best to start fresh and not worry about taking any chance. Donate the stuff to Goodwill or your neighbor or the chuch kitchen.

~Laura

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. - JoJo0611 replied to JoJo0611's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      4

      CT with contrast.

    2. - Scott Adams replied to Ginger38's topic in Related Issues & Disorders
      2

      Shingles - Could It Be Related to Gluten/ Celiac


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,398
    • Most Online (within 30 mins)
      7,748

    Megannnnn
    Newest Member
    Megannnnn
    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

    • JoJo0611
      I didn’t know there were different types of CT. I’m not sure which I had. It just said CT scan with contrast. 
    • Scott Adams
    • Scott Adams
      I had the same thing happen to me at around your age, and to this day it's the most painful experience I've ever had. For me it was the right side of my head, above my ear, running from my nerves in my neck. For years before my outbreak I felt a tingling sensation shooting along the exact nerves that ended up exactly where the shingles blisters appeared. I highly recommend the two shot shingles vaccine as soon as your turn 50--I did this because I started to get the same tingling sensations in the same area, and after the vaccines I've never felt that again.  As you likely know, shingles is caused by chicken pox, which was once though of as one of those harmless childhood viruses that everyone should catch in the wild--little did they know that it can stay in your nervous system for your entire life, and cause major issues as you age.
    • trents
    • Clear2me
      Thanks for the info. I recently moved to CA from Wyoming and in that western region the Costco and Sam's /Walmart Brands have many nuts and more products that are labeled gluten free. I was told it's because those products are packaged and processed  in different  plants. Some plants can be labeled  gluten free because the plant does not also package gluten products and they know that for example the trucks, containers equipment are not used to handle wheat, barely or Rye. The Walmart butter in the western region says gluten free but not here. Most of The Kirkland and Members Mark brands in CA say they are from Vietnam. That's not the case in Wyoming and Colorado. I've spoken to customer service at the stores here in California. They were not helpful. I check labels every time I go to the store. The stores where I am are a Sh*tshow. The Magalopoly grocery chain Vons/Safeway/Albertsons, etc. are the same. Fishers and Planters brands no longer say gluten free. It could be regional. There are nuts with sugar coatings and fruit and nut mixes at the big chains that are labeled gluten free but I don't want the fruit or sugar.  It's so difficult I am considering moving again. I thought it would be easier to find safe food in a more populated area. It's actually worse.  I was undiagnosed for most of my life but not because I didn't try to figure it out. So I have had all the complications possible. I don't have any spare organs left.  No a little gluten will hurt you. The autoimmune process continues to destroy your organs though you may not feel it. If you are getting a little all the time and as much as we try we probably all are and so the damage is happening. Now the FDA has pretty much abandoned celiacs. There are no requirements for labeling for common allergens on medications. All the generic drugs made outside the US are not regulated for common allergens and the FDA is taking the last gluten free porcine Thyroid med, NP Thyroid, off the market in 2026. I was being glutened by a generic levothyroxin. The insurance wouldn't pay for the gluten free brand any longer because the FDA took them all off their approved formulary. So now I am paying $147 out of pocket for NP Thyroid but shortly I will have no safe choice. Other people with allergies should be aware that these foreign generic pharmaceutical producers are using ground shellfish shell as pill coatings and anti-desicants. The FDA knows this but  now just waits for consumers to complain or die. The take over of Wholefoods by Amazon destroyed a very reliable source of good high quality food for people with allergies and for people who wanted good reliably organic food. Bezos thought  he could make a fortune off people who were paying alot for organic and allergen free food by substituting cheap brands from Thailand. He didn't understand who the customers were who were willing to pay more for that food and why. I went from spending hundreds to nothing because Bezo removed every single trusted brand that I was buying. Now they are closing Whole foods stores across the country. In CA, Mill Valley store (closed July 2025) and the National Blvd. store in West Los Angeles (closed October 2025). The Cupertino store will close.  In recent years I have learned to be careful and trust no one. I have been deleberately glutened in a restaurant that was my favorite (a new employee). The Chef owner was not in the kitchen that night. I've had  a metal scouring pad cut up over my food.The chain offered gluten free dishes but it only takes one crazy who thinks you're a problem as a food fadist. Good thing I always look. Good thing they didn't do that to food going to a child with a busy mom.  I give big tips and apologize for having to ask in restaurants but mental illness seem to be rampant. I've learn the hard way.          I don't buy any processed food that doesn't say gluten free.  I am a life long Catholic. I worked for the Church while at college. I don't go to Church anymore because the men at the top decided Jesus is gluten. The special hosts are gluten less not gluten free. No I can't drink wine after people with gluten in their mouth and a variety of deadly germs. I have been abandoned and excluded by my Church/Family.  Having nearly died several times, safe food is paramount. If your immune system collapses as mine did, you get sepsis. It can kill you very quickly. I spent 5 days unconscious and had to have my appendix and gall bladder removed because they were necrotic. I was 25. They didn't figure out I had celiac till I was 53. No one will take the time to tell you what can happen when your immune system gets overwhelmed from its constant fighting the gluten and just stops. It is miserable that our food is processed so carelessly. Our food in many aspects is not safe. And the merging of all the grocery chains has made it far worse. Its a disaster. Krogers also recently purchased Vitacost where I was getting the products I could no longer get at Whole Foods. Kroger is eliminating those products from Vitacost just a Bezos did from WF. I am looking for reliable and certified sources for nuts. I have lived the worst consequences of the disease and being exposed unknowingly and maliciously. Once I was diagnosed I learned way more than anyone should have to about the food industry.  I don't do gray areas. And now I dont eat out except very rarely.  I have not eaten fast food for 30 years before the celiac diagnosis. Gluten aside..... It's not food and it's not safe.  No one has got our backs. Sharing safe food sources is one thing we can do to try to be safe.        
×
×
  • 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.