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

Not Eating


armywife

Recommended Posts

armywife Newbie

Hi, everyone. My daughter just turned 2, she was diagnosed with celiac when she was 20 mo. We first knew somthing was wrong when she stared loosing weight and throwing up every couple of days for no apparent reason, she wouldnt eat anything but bread and pasta (no wonder she was sick so much), but after putting her on the gluten-free diet she starting eating like she had never tasted food before, we were so happy...she gained 4 lbs in the first 4 months. But she is back to her old ways...i cant get her to eat anything (although not throwing up). My husband is in the army and is deployed right now, I dont know if that has something to do with it (shes a big time daddys girl). She did good the first couple of months he was gone, but not anymore. She keeps telling me that her stomach hurts, but im pretty sure im not giving her anything she shouldn't have. I try to explain to her that if she eats her tummy wont hurt, but i cant get through to her. No matter what i try i cant get her to eat. All she wants to do is drink. I wont give her the cup until she has eaten but im scared that is going to dehydrate her since she will only eat literally one bit of every meal. i dont know what to do, any suggestions? Has anyone else had a similar situation? Her attitude has gotten much worse within the last months also, there could be many factors causing this though. Daddy being gone, terrible two's....but could this have something to do with it also?

by the way what is corn gluten...can she have that since it is not wheat gluten?


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



Celiac.com Sponsor (A8-M):



jayhawkmom Enthusiast

I think all children go through periods where they'll eat more (or less) than other times. My son is almost 15 months old, and is going through the same thing. Although, he sure doesn't tell me if he has a tummy ache, he can't vocalize that well yet.

Since you mention corn... I'm wondering if you are keeping all forms of "bad" gluten (rye, barley, oats) away from her as well. If not, you need to be steering clear of all of those other grains. Corn is ok for Celiacs, but is a highly allergic grain, in and of itself.

I can't imagine how difficult it must be to have your husband deployed. I hope he returns home safely, soon!

2kids4me Contributor

We just recently discovered Kathryn was lactose intolerant (she's 13), she has been gluten free for 3 years and I thought for awhile she was getting glutened somewhere, nausea, stomach aches, decreased appetite. I omitted dairy for several days then gave her some milk - she was sick within hours, so then (with great advice on this board), I waited til she was well again and offered lactose free milk - tada - no sick!

Lactose intolerance is common with celiac. So is a casein allergy/intolerance - if Kathryn became ill with lactose free milk, then I would have assumed acasein problem...

one thing to try anyway.

She sould be able to have water if she wants her cup, 2 year olds - gosh - I remember that! Loved carrots and sweet potatoes... gobbled them up... then one day... no way, no way did she want to eat anything orange, she decided she didnt like orange foods. groan...

good luck and let us know how things are going. Safe travels for hubby

Sandy

Ellen Newbie
Since you mention corn... I'm wondering if you are keeping all forms of "bad" gluten (rye, barley, oats) away from her as well. If not, you need to be steering clear of all of those other grains. Corn is ok for Celiacs, but is a highly allergic grain, in and of itself.

It sounds like some type of food allergy. But it may not be related to Celiacs at all. I am personally going through getting tested for eosinophilic esophagitis (EE) in addition to Celiacs. My oldest daughter (5.5 YO) has a ton of issues...mostly sloved by putting her on a gluten free/caisen (milk protein) free diet. Her reflux is starting to act up again so we're thinking of having her tested for EE as well. My vague understanding of EE is it's acid reflux caused by an allergy...most likely food. I'll have the diagnosis for myself hopefully Monday (11/21). Then they test me for waht the aditional allergy is. Then I can get a real understanding of it first hand so I know what my daughter is going through. She's non-verbal so sh doesn't really let me know when her stomach is upset or how.

In addition to this Celiacs tend to get a ton of other allergies...mostly in the grain category. One thing that is safe for Celiacs to eat but you may want to avoid for awhile is buckwheat. It is closely related to wheat but dosen't have the same chemical structure and therefore doesn't have true gluten in it...similar to corn. This contains a substance that is similar to gluten, but is digestiable by Celiacs. You may want to just try eliminating stuff till you find out what's bugging her. My 10 year old nephew was put on the infant diet of food introduction when he was first diagnosed. They took him off everything except rice and slowly...once a month...added a new grain till he was back up to the regular Celiac diet. I hope for your sake you don't have to go through that!

Guest cassidy

I know that I had ups and downs when I first when gluten-free. I did well in the beginning and then I had gastritis and my stomach hurt when I ate anything. I figured out (much later) that I can't have nightshades and when I do they really upset my stomach to the point there everything I eat makes it hurt. When that happens all I want to do is drink. I drink a lot of kefir (like liquid yogurt), boost (not chocolate malt) and carnation instant breakfast (powdered kind only, not chocolate malt).

I would listen to her and trust that she is telling the truth. I don't know if pediasure is gluten-free, or any kids supplements but I know the ones I listed above are ok.

I realize that it can be hard to communicate with kids and hard to tell what is causing their problems but if you tried feeding her anyway and that isn't working, why not try listening to her and giving her nutritious drinks.

Maybe you can keep a food diary and see if there are things she likes and doesn't like. If she will drink the carnation in milk, then milk probably isn't bothering her.

Lots of us have discovered other allergies/intolerances after going gluten-free.

Guest nini

buckwheat is not closely related to wheat at all, it is part of the rhubarb family and is a berry. It is NOT a grain and is not related to wheat.

My daughter certainly went through plenty of stages of refusing to eat. We didn't get her on the gluten-free diet until she was 3 though, if she's complaining that her tummy hurts I try two things, get her to go to the bathroom or eat something. Yes it's hard to get them to eat when they equate food with tummy hurting and at that age it's difficult for them to express what foods sound good to them and what don't. Try the simple things like bananas, applesauce, rice, and maybe some gluten-free crackers or toast and see if you can't get her to eat something basic.

almostnrn Explorer

I wouldn't rule out the issue that her father is deployed. We have been through that personally and sometimes it seems for us like there is a delayed reaction before the reality sets in. Its hard with your daughters age because she may not be able to verbalize her feeling about daddy being gone. Also it is a pretty abstract idea that he is so far away...I know it was hard for mine and they were much older. I'm sure that it wears on you too. Its hard not only to be home by yourself trying to take care of things but then the worry of him being ok. I will be praying for your family and your husbands safe return.

As far as getting your daughter to eat, have you by chance tried to have small "snack" type items available all the time? gluten-free cereal in a bowl, fruit, etc. I know its a horrible habit to get into not eating at the table but I found when my kids went through those times of not eating I could sneak in a snack during a favorite show without them even realizing what was going on. Hope this helps!


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



Celiac.com Sponsor (A8-M):



key Contributor

I would try no dairy. Since she was doing so well before and her tummy hurts. Does she eat out? DOes she go to daycare?? It does sound like she could be getting gluttened somewhere. It is hard to know.

It is hard on you to have to deal without a husband. Hang in there.

Monica

Ursa Major Collaborator

Armywife, I had the same problem as your daughter. A year ago in October I eliminated gluten, which stopped the chronic diarrhea within a day, and my terribly fibromyalgia pains went away within two weeks (when I eliminated all lectins, of which gluten is one). My stomach aches took about a month to completely go away.

It looked like I had found my answers. Then, three months later, all my muscle pains returned. Through an elimination diet I found out I am intolerant to salicylates, too.

Why did I appear to get well at first, and then got worse again after three months?

I believe that when the villi are too damaged to absorb nutrients, they don't absorb the good ones, or a lot of the 'bad' ones (meaning, many things we're intolerant to). At first, eliminating all the lectins was enough. But when the villi healed, and started absorbing the salicylates properly, I was in trouble again and needed to eliminate those.

It sounds like your daughter did great for a few months, but now the villi are healed enough that something else is bothering her, giving her a tummy ache.

You need to try an elimination diet to find out what the problem food(s) is. I suggest you eliminate all dairy, corn and soy for starters, to see if that helps. If she feels better, keep those foods away from her for a month, and then try them one at a time (at least a week apart to catch any delayed reactions) to see what happens. Eliminate the ones (if any) she reacts to for at least a year before trying them again. If they remain a problem after a year, eliminate them for life.

If taking those foods out of her diet won't make a difference within two weeks, try other things that are likely culprits, like eggs or nightshades (potatoes, tomatoes, peppers, eggplant) and nuts.

Hopefully it is just dairy and/or soy (the most common allergens/intolerances for people with celiac disease), otherwise you'll have to keep looking until you figure it out. Don't dismiss your daughter's complaints of a tummy ache as just psychological, especially after eating so well for four months.

kbtoyssni Contributor

Corn gluten is ok. Gluten is used to refer to the protien in a grain so you've got wheat gluten, corn gluten, rye gluten, etc. Only the gluten in WBRO is harmful to celiacs, although I agree that it's a bit unsettling when someone refers to corn gluten :)

armywife Newbie

Thanks everyone for your suggestions, after reading some of the other discussions on here, im thinking that I might not be all gluten out of her diet. I never thought of checking bandaids and paper towels. Just yesterday I realized that i was giving her vitamins with gluten. I feel like such a horrible mother. Did anyone else have this much trouble starting out with the diet? I really need to find a support group around here. Does anyone live in NC and know of one around Fayetteville? I found a number on this website, but when I called it the man said i had the wrong number??

ArtGirl Enthusiast
Did anyone else have this much trouble starting out with the diet?

Oh, yes. If it weren't for this forum I'd still be struggling. There are so many places to look for gluten, like dog food and hand lotion. And vitamins - gosh, I must have thrown away a hundred dollars in supplements and vitamins after learning that they had gluten in them (and corn - I have a corn allergy, which I didn't isolate until some time after going gluten-free).

Don't be too hard on yourself - it's takes time to learn everything and totally eliminate gluten - I'd think it is especially hard with young children who can't communicate well yet.

Ursa Major Collaborator
Thanks everyone for your suggestions, after reading some of the other discussions on here, im thinking that I might not be all gluten out of her diet. I never thought of checking bandaids and paper towels. Just yesterday I realized that i was giving her vitamins with gluten. I feel like such a horrible mother. Did anyone else have this much trouble starting out with the diet? I really need to find a support group around here. Does anyone live in NC and know of one around Fayetteville? I found a number on this website, but when I called it the man said i had the wrong number??

You're not a horrible mother. If doctors would be more knowledgeable and give you better information, we wouldn't have to figure it all out on our own.

Others here will know of good brands for children's vitamins that are gluten-free.

Have you checked shampoo, conditioner, bubble bath, toothpaste, soap, lotion etc. for gluten? It will hide in all kinds of things. Also, have you bought your daughter her own toaster, only to be used for gluten-free bread? Toasters are a source of cross-contamination. As are plastic colanders. Never drain gluten-free noodles with a colander that has been used for wheat noodles, you can absolutely not get it clean enough to be safe.

It is tricky. You will figure it out in the end. I hope that maybe her vitamins are the answer. But it would be a good idea to eliminate dairy, at least for a while, anyway. Because most celiacs can't tolerate dairy for at least six months to a year when going gluten-free, because of lactose intolerance (caused by damaged villi). Many have a casein intolerance, though, and won't ever be able to have dairy products again.

I hope your daughter feels better soon.

azmom3 Contributor

ditto what almostnrn said...small snacks throughout the day as opposed to or in addition to meals. My son is 26 months and we have had to resort to this to help him put on some weight. It takes him a really, really long time to eat even a small amount and many times he takes 1 or 2 bites and says "all done." We just keep offering as often as we can and it has made a difference for us. Also, another person posted about eosinophilic esophagitis...my son is also being tested for this. It wouldn't hurt to look into it. If you haven't done allergy testing yet, it might be worth it. If your child isn't showing allergy problems at all, then I would say that eosinophilic esophagitis is probablyl not the problem, but if there are some allergies, then it might be worth looking into it. This is a fairly new problem they're seeing and it's been on the rise. Good luck!

moomama18 Newbie

I would say the same as others here as far as hidden glutens. I had the same experience with her vitamins. She now takes two to get all the vitamins and minerals she needs. I also had to switch her soap/lotion. Once I did that, it eliminated a lot of issues for us. Fortunately for me, eating has never been an issue for her - she loves to eat.

I would also say that your husband being away might have some impact but I would worry mostly about the hidden glutens. Hang in there, it gets easier with time. It may seem hard at first, but there are many battles that are worse.

I'm in MD, not NC but not so far if you have any questions or need help.

Michelle

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.