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

Going Gluten-Free In Sympathy With Your Kids?


kb27

Recommended Posts

kb27 Apprentice

My 8-yr-old son was diagnosed with celiac via blood test. We will be going gluten-free soon (after next GI appt). We have decided to make the whole kitchen gluten-free, at least initially, so that he will have a safe place where he can eat anything. And we don't have to worry about cross-contamination.

I have considered going gluten-free with him at least for a few months, so that he has a buddy in all of this. It doesn't seem like it would be so hard, given that we will be completely gluten-free at home - I just can't partake outside the home either. I tested negative for celiac, and have no big GI issues (just gas and bloating). In other words, I don't have any reason to believe that I have a gluten intolerance.

Is it fine for a non-celiac/gluten intolerant to go gluten-free for awhile? Or do you lose the ability to digest gluten?

Has anyone else gone gluten-free to support your child? Even though you don't have to?


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



Celiac.com Sponsor (A8-M):



domesticactivist Collaborator

It is totally fine to go gluten-free in solidarity with your child. Our family took that approach and it made a positive impact for our son emotionally and physically. Having a gluten free house makes it much easier to stay safe.

It's good you've already been tested. IMO anyone who plans to go gluten-free should get screened for celiac first. I didn't, and a year later ended up doing a miserable gluten challenge so I could get tested.

People who don't have a problem from gluten don't end up developing one by going gluten free. There are ways other than celiac to be affected by gluten that your tests would not have shown. Some people who don't have celiac even get withdrawal symptoms when cutting out gluten. Some people find that reintroducing gluten exposes problems they have with it. If you cut it out and then experience symptoms from reintroducing it, I think you shouldn't have been eating it in the first place. Many people can go back and forth between gluten free and eating gluten without any problem.

faithforlife Apprentice

Yeah we had 2 families go gluten free for us in support of us and have since realized that they just feel better all around on a gluten-free diet and even began to be able to digest lactose better. So, they are for the most part gluten-free still and it's been almost 12 months! But I've wondered the same question of what are the long term effects of my non celiac kids going gluten-free. The GI told me though that it's just a matter of time before they very possibly develop celiac and that it is crucial they learn the diet and how rigid it is and cope with all the emotions of going without NOW. And who knows their kids some day could get celiac, too.

Darn210 Enthusiast

I've done a couple of trial diets . . . one for 6 weeks and one for 6 months. I had no problems going off and then back on.

I've done (temporary) gluten free with my daughter at times . . . when it's most difficult for her . . . On vacations or just a trip to a restaraunt. At restaraunts (especially if it's someplace we haven't gone before), I'll get something different from her so if she doesn't like what she got, she can have some of mine.

missy'smom Collaborator

My son and I were both already gluten-free when we learned of his corn allergy. Corn is in everything too. I went corn-free in support of him. He didn't have severe symptoms so it was hard for him to be motivated and I felt it would be so mean to eat corn-chips etc in front of him. I did have canned chicken with cornstarch in it but he has no personal feelings about canned chicken;) LOL. It was something I ate when he was at school-for lunch. I didn't eat out of the house much but if I had and he wasn't with me, I'd have corn containing things-but wouldn't mention it. There were so many gluten-free products that were corn containing that I went without, even though I have so many other restrictions as well. That limited my diet quite a bit more but it was worth it for him and his tested reactivity went down as a result of good avoidance-that won't happen with gluten but can with allergies.

So yes, I encourage you to go gluten-free with your kiddo, keeping in mind the testing issues for yourself that others mentioned.

There are LOTS of gelatin/jello and pudding based and fruit desserts out there that are already gluten-free or easily modified that are good when you are starting out and not ready to jump into gluten-free baking. We made 12+ layer rainbow jello one Christmas instead of cookies and my kid thought it was THE best thing EVER. He's still taking about it a couple years later. There are all kinds of cool mold too-eggs for Easter, a brain mold for Halloween...

xjrosie Apprentice

I have three daughters, two of which have celiac disease. My third daughter just had her bloodwork done yesterday and we're waiting now. But, I have already decided that once my daughter is fully tested for Celiac (at the doctor's discretion) I will be going completely gluten-free in our house. I want at least one place in this world where they can come in and grab anything they want without worry of being sick.

Besides, a gluten-free diet is actually really healthy. It will be more of a benefit than a burden.

researchmomma Contributor

Great question! I am gluten-free with my daughter who is gluten intolerant (both sides of our family are).

I decided to do it with her so I could feel the peer pressure (you wouldn't believe how many of my friends will say "she won't know if you eat it" :rolleyes: ), has an ally and I am interested in finding good tasting food for us both.

That gas and bloating you have may just go away. ;)

What I have found with going gluten free is that I feel better and part of that is because I don't eat things with a label full of random ingredients. Like ice cream for example: cream, sugar, vanilla....done. What is all that other crap?

My daughter and I cook together which is nice. When we go to a restaurant, we figure out what we are going to get that is gluten-free together. Much better than her being different and alone. She loves that I support her in this and my husband supports it too ( I was a little surprised at this but my daughter gets really sick from gluten and he doesn't want to see that side of her).


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



Celiac.com Sponsor (A8-M):



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

      Newly diagnosed mam to coeliac 11 year old

    2. - tiffanygosci posted a topic in Introduce Yourself / Share Stuff
      0

      Celiac support is hard to find

    3. - cristiana replied to hjayne19's topic in Traveling with Celiac Disease
      2

      Mallorca Guide

    4. - hjayne19 replied to hjayne19's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      7

      Insomnia help

    5. - cristiana replied to hjayne19's topic in Traveling with Celiac Disease
      2

      Mallorca Guide

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

    • Total Members
      132,946
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Posts

    • Dizzyma
      Hi Trent and Cristiana, thank you so much for taking the time out to reply to me.  My daughters GP requested bloods, they came back as showing a possibility of celiac disease, she advised me to continue feeding gluten as normal and wait on a hospital appointment. When we got that the doctor was quite annoyed that the gp hadn’t advised to go gluten free immediately as she explained that her numbers were so high that celiac disease was fairly evident. That doctor advised to switch to a gluten-free diet immediately which we did but she also got her bloods taken again that day as it made sense to double check considering she was maintaining a normal diet and they came back with a result of 128. The hospital doctor was so confident of celiac disease that she didn’t bother with any further testing. Cristiana, thank you for the information on the coeliac UK site however I am in the Rrpublic of Ireland so I’ll have to try to link in with supports there. I appreciate your replies I guess I’ll figure things as we go I just feel so bad for her, her skin is so sore around her mouth  and it looks bad at an age when looks are becoming important. Also her anxiety is affecting her sleep so I may have to look into some kind of therapy to help as I don’t think I am enough to help. thanks once again, it’s great to be able to reach out xx   
    • tiffanygosci
      I have been feeling so lonely in this celiac disease journey (which I've only been on for over 4 months). I have one friend who is celiac, and she has been a great help to me. I got diagnosed at the beginning of October 2025, so I got hit with all the major food holidays. I think I navigated them well, but I did make a couple mistakes along the way regarding CC. I have been Googling "celiac support groups" for the last couple days and there is nothing in the Northern Illinois area. I might reach out to my GI and dietician, who are through NW Medicine, to see if there are any groups near me. I cannot join any social media groups because I deleted my FB and IG last year and I have no desire to have them back (although I almost made a FB because I'm desperate to connect with more celiacs). I'm glad I have this forum. I am praying God will lead me to more people to relate to. In my opinion, celiac disease is like the only food- related autoimmune disease and it's so isolating. Thanks for walking alongside of me! I'm glad I know how to help my body but it's still not easy to deal with.
    • cristiana
      Forgot to add...  Quite a lot of 'tapas' are gluten free. Ones to look for:  Tortilla de patata (a thick omelette made with potatoes and onions) should be 'sin gluten', and chorizo cooked in red wine makes a nice dish.  Look out for sobrasada, which is very Mallorcan, a softer type of sausage/pate which you can spread on gluten free crispbread which you should be able to buy for supermarkets.  Until very recently we could not buy it here in the UK but we've managed to find a local source, and Lidl have started to sell it in tubs, too. Here's more info on it: Sobrasada is a soft, spreadable, cured pork sausage from Spain's Balearic Islands (like Mallorca), distinguished by its reddish color from paprika, sweet-spicy flavor, and pâté-like texture, perfect for spreading on toast, cooking into dishes like eggs or pasta, or drizzling with honey. Its unique texture comes from the island's humid climate preventing full drying, resulting in a semi-soft sausage that's gently aged, unlike drier mainland chorizo.
    • hjayne19
      Hi @cristiana   Thank you so much for your reply. This is so helpful. I definitely suffer from anxiety mostly related to health. Brain fog definelty doesn’t help this when it comes. I find my 4 am wake ups are potentially more food related if that’s a possibility (eating enough carbs with protein and fats) and if I eat a small snack before bed to hold throughout the night. I just haven’t been able to help the sudden increase in more days where I can’t fall asleep for hours - it’s those racing thoughts like you describe. I feel like a machine that’s running and can’t shut down.    I will try the epsom salt bath that’s a great suggestion. I think I’m probably working through some other food triggers that may be contributing as well with brain fog.    Anyways sorry to go off. It feels so reassuring finding this community and being able to chat with others. I was definitely feeling a bit crazy until I realized there are many others going through the same thing. 
    • cristiana
      Hi Jayne Great choice for a gluten-free cycling holiday, I know the island well. The words you need to look for are 'sin gluten' when you are out and about.   I think you will be amazed at how many packets and canned goods are clearly labelled 'sin gluten' in the supermarkets - many more than one sees here - often in quite large type.  There seems to be a thought in the UK that if you label something gluten free it will affect flavour etc and will put people off buying it!  However, in the case of Spain, it is almost as if the the Spanish see it as an endorsement of quality and flavour!  There is a supermarket called Mercadona and they label their produce very clearly. Paella should be gluten free so long as the chef use the right stock such as Knorr or a gluten-free homemade stock - you can check.  Most Mallorquins in catering speak English but if not, ask, "Contiene gluten?"  Tumbet is a wonderful dish if you like peppers, tomato, aubergines, garlic and olive oil!  A sort of variation on ratatouille.   Slow roast lamb shank should be safe, and there are endless fish dishes to choose from and salads.  Flan is made with eggs, sugar and caramel, and should be gluten-free.  Lots of gluten-free ice cream and sorbets, they should be clearly labelled. If you want specific restaurant recommendations, feel free to PM me. Cristiana    
×
×
  • 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.