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.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,635
    • Most Online (within 30 mins)
      7,748

    dysmathers
    Newest Member
    dysmathers
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • deanna1ynne
      Dd10 was tested for celiac four years ago bc two siblings were dx’d (positive labs and biopsies). Her results at the time were positive ema  and ttg (7x the UL), but a negative biopsy. We checked again three months later and her ttg was still positive (4x the UL), but ema and biopsy were negative. Doc said it was “potential celiac” and to keep eating gluten, but we were concerned about harming her growth and development while young and had her go gluten-free because we felt the labs and ema in particular were very suggestive of early celiac, despite the negative biopsies. She also had stomach aches and lethargy when eating it. We just felt it’d be better to be safe than sorry. Now, four years later, she doesn’t want to be gluten-free if she doesn’t “have to be,” so underwent a 12 week gluten challenge. She had labs done before starting and all looked great (celiac panel all negative, as expected.) Surprisingly, she experienced no noticeable symptoms when she began eating gluten again, which we felt was a positive sign. However, 12 weeks in, her labs are positive again (ttg 4x the UL and ema positive again as well). Doc says that since she feels fine and her previous two biopsies showed nothing, she can just keep eating gluten and we could maybe biopsy again in two years. I was looking up the ema test and the probability of having not just one but two false positives, and it seems ridiculously low.  Any advice? Would you biopsy again? She’s old enough at this point that I really feel I need her buy-in to keep her gluten-free, and she feels that if the doc says it’s fine, then that’s the final word — which makes me inclined to biopsy again and hope that it actually shows damage this time (not because I want her to have celiac like her sisters, but because I kind of think she already does have it, and seeing the damage now would save her more severe damage in the long run that would come from just continuing to eat gluten for a few more years before testing again.)  Our doc is great - we really like him. But we are very confused and want to protect her. One of her older sibs stopped growing and has lots of teeth problems and all that jazz from not catching the celiac disease sooner, and we don’t want to get to that point with the younger sis. fwiw- she doesn’t mind the biopsy at all. It’s at a children’s hospital and she thinks it’s kind of fun. So it’s not like that would stress her out or anything.
    • Inkie
      Thanks for the replies. I already use a gluten-free brand of buckwheat flakes I occasionally get itchy bumps. I'm still reviewing all my food products. I occasionally eat prepackaged gluten-free crackers and cookies, so I'll stop using those. I use buckwheat flakes and Doves Farm flour as a base for baking. Would you recommend eliminating those as well? It's a constant search.
    • Wheatwacked
      Gluten free food is not fortified with vitamins and minerals as regular food is.  Vitamin deficiencies are common especially in recently diagnosed persons,  Get a 25(OH)Vitamin D blood test. And work on raising it.  The safe upper blood level is around 200 nmol/L.    "Low serum levels of 25(OH)D have been associated with increased risk of autoimmune disease onset and/or high disease activity. The role of vitamin D in autoimmune diseases   🏋️‍♂️Good job!   I find the commercial milk will give me mild stomach burn at night, while pasture/grassfed only milk does not bother me at all.  While you are healing, listen to your body.  If it hurts to eat something, eat something else.  You may be able to eat it later, or maybe it is just not good for you.  Lower your Omega 6 to 3 ratio of what you eat.  Most omega 6 fatty acids are inflammation causing.    The standard american diet omega 6:3 ratio is estimated at upward of 14:1.  Thats why fish oil works
    • Inkie
      I  notice a reaction to tea bags, possibly due to gluten or other substances. Is this recognizable?
    • trents
      The blood tests you had done are not the main ones. The two main ones are the "Total IGA" (to check for IGA deficiency) and the "TTG-IGA". Current guidelines for the "gluten challenge" when people have been gluten free for a significant time period are the daily consumption of at least10g of gluten (about the amount in 4-6 slices of wheat bread) for at least two weeks leading up to the day of the blood draw. That should give you some perspective.
×
×
  • 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.