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

Skinny 2 Year Old


ItchyMeredith

Recommended Posts

ItchyMeredith Contributor

Hello- I wanted to run this by all of you experienced celiac parents to get your advice. I have celiac and I am trying to find out if my LO does too.

Kellen is my oldest. He is 2 1/2 years old. He is really thin and a little short as well. He is 36 inches (25-50th percentile) and 27 pounds (10-20 percentile). His father and I are not small people. I am 5'8" and my DH is 5'11"- neither of us are skinny.

I am a little worried about my little guy. He eats ALL DAY LONG. I am not exaggerating. From the moment he wakes up to the moment he goes to bed he asks for food. I feel like I am a short order cook. The good news is that he loves healthy food but he eats in excess. I have never seen such a bottomless pit. So why is he so tiny? He does have food allergies and sensitivities that have been mostly identified but I fear that there may be more. I am trying to rule out celiac disease (something I have) but I have read that the tests are not that accurate in kids so young. He already passed one blood panel a couple of months ago but he has never consumed much gluten so I don't know how good that test was for him.

What do you think?

Thanks in advance!

***A couple of weeks ago I found a brown spot on his front tooth that looks a lot like the enamel defects I have read about.

****He was born big BTW at 9.5 lbs but fell down to the 10 and 20th percentiles in weight within the first 6 months.


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



Celiac.com Sponsor (A8-M):



Guest j_mommy

Is he consitantly growing?????? I mean...is he on the same growing curve????

Ursa Major Collaborator

I say there is definite reason for concern, and I would guess that he is gluten intolerant as well.

I have a grandson who grew consistently (Ethan is five now), but was so skinny you could see every rib. This boy was ALWAYS hungry and would ask for food every few minutes. I was there at meals quite a few times, and he was never full. My daughter would eventually say that he had enough to eat, and would refuse to give him more, and he would cry. Poor little guy.

He also started having pains in his legs when he was three, and was very emotional. Whenever he hurt himself, or sometimes just when somebody looked at him the wrong way, he would cry for hours and would be inconsolable. My daughter decided that he was a little wimp and would often not comfort him, as to not encourage his wimpiness. He also never had regular, formed BMs.

About three months ago, just so I would stop bugging her about it, she put him on a gluten-free diet. What a difference! Immediately he stopped being so emotional. When he hurts himself he might cry for a couple of minutes, like other kids, and will then go back to being happy. His leg pains went away, and within a couple of days he had his first solid BM ever.

Just six months ago, when I visited, he jumped into my arms from the stairs, a few steps up. He was so light it scared me!

I visited last weekend, and when I lifted him up to say good-bye, I was delighted to find that he was heavy! He is still slender (all my grandkids are, and all my kids were), but he has a normal weight now. I am so happy!

So, I say follow your instincts on this one and forget about blood work. Put him on the gluten-free diet to see if it will make a difference. And while you are at it, cut dairy out, too (my grandson is intolerant to dairy and nightshades as well).

I say if a skinny kid eats and eats, there is a problem. By the way, my son is like that, too. He is 24 and married and won't listen to me, unfortunately. But I am sure he is also dairy and gluten intolerant. One of these days, when I have the money, I will have him tested by Enterolab. He agreed that he would cooperate if I pay for it. He is a very normal height at 6 feet. He always grew, but was way too skinny, had those leg pains and still is a bottomless pit when it comes to food. And he is the worst scatter brain ever.

I just wished I would have known about gluten when my kids were little! I think every one of them has a gluten problem. My oldest daughter (little Ethan's mom) has finally made her family gluten-free (except for her husband, who won't give up gluten). She says that she has so much more energy without gluten.

ItchyMeredith Contributor

Thanks for your advice. Can you do Enterolab on a 2 year old?

Ursa Major Collaborator
Thanks for your advice. Can you do Enterolab on a 2 year old?

Yes, absolutely, that is a great idea! Then you would have definitive answers, anyway. You would also know if dairy and soy are a problem as well.

Owen'sMom Rookie

I have a little peanut myself. My son is almost 2 1/2 years old and is 34 inches tall and weighs about 26.5lbs. Which also puts him low in the percentiles, I'm not too concerned though as he used to be FTT last year and wasn't even on the charts.

He was born at 7lbs13oz and was 20 inches, which is about 50 percentile. Than by 4 months he was up to the 70th, but after we introduced solids he started falling off the charts.

My son also constantly asks about food all day long and yet doesn't put a lot of weight on, he can actually outeat his 7yr old brother.

We are still undergoing testing at the moment and it's tough as we are stationed overseas in Germany. I'm german but the german doctors are of no help with all the problems.

We had him tested through enterolab and it said he has a casein and gluten intolerance, yet the german doctors don't take this as a diagnosis.

In the next month or so we'll be heading to Walter Reed and get him scoped to figure out what is wrong on his inside and hopefully make him feel better.

goldyjlox Contributor

My daughter is 3 /12 and she is exactly the same...super skinny and is always asking for food. She doesnt have regular BM either. She is irratable and sometimes looks a bit sickly but she is fine otherwise. I asked my doctor about it and he doesnt seem concerned about her weight, she is 34.4 lbs and in the 50th% for her weight. Since I just got DX I am concerned about my kids, my son is almost a year and he has rashes in his diaper now for 8 weeks and they are not diaper rashes. Both my kids have been refered to a Pediatric Allergin.

I would talk to your doctor...I am concerned about my daughter and I am going to have the bloodtest done as hard as that will be. And I am decreasing the Gluten in her diet.


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



Celiac.com Sponsor (A8-M):



Ursa Major Collaborator

Owen's mom and Jess, you both know there is a problem, and you suspect it is gluten. You absolutely DO NOT need a doctor's permission to remove gluten from your children's diet! If it makes a difference, you know what the problem is, and it doesn't matter what the doctor says. The gluten-free diet is very healthy, nobody needs any grains at all to be well, that is a myth perpetuated by the grain industry. Of course they want to sell their products!

And if Enterolab says a kid is intolerant to dairy and gluten, why waste the money you spent on these tests, by not taking them seriously, just because a doctor doesn't? A lot of doctors are terribly ignorant on these issues. Why have kids suffer because of that?

My oldest daughter finally just made all her kids gluten-free, and couldn't care less what any doctor says. Her kids feel better, that's all that counts. Please do your children a favour, and do the same.

kevieb Newbie

ladies, i am in the same boat with my youngest child. she very skinny---you can see all her ribs, she gets rashy on her behind, (but it does not look like DH) it comes and goes. sylvia also had brown horizontal ridges across her front teeth. she had 6 teeth crowned a few months after she turned 3---they worked on 12 teeth total. the dentist told me she has enamel hypoplasia. she does not appear to be getting any further damage to her teeth. she is a wild, squirrly, happy little girl, but i do worry whether or not she could have celiac disease. so far, she has tested negative. she had health problems and was FTT until she was 2. they tell me that this could also be the cause of her teeth problems. all of our meals are gluten free, but i do keep certain wheat-based things around for the non-celiacs at home. i guess this means sylvia is gluten-light. at this time, i choose not to put her gluten free because it is important to me to have an actual diagnosis and she is doing well. i will probably have her tested for celiac again soon, and will probably continue to check her on a regular basis.

just like my daughter, your kids seem to have little things that indicate the possibility of celiac disease, and we know it is a real possibility since we already have diagnosed family members.

gfpaperdoll Rookie
Owen's mom and Jess, you both know there is a problem, and you suspect it is gluten. You absolutely DO NOT need a doctor's permission to remove gluten from your children's diet! If it makes a difference, you know what the problem is, and it doesn't matter what the doctor says. The gluten-free diet is very healthy, nobody needs any grains at all to be well, that is a myth perpetuated by the grain industry. Of course they want to sell their products!

And if Enterolab says a kid is intolerant to dairy and gluten, why waste the money you spent on these tests, by not taking them seriously, just because a doctor doesn't? A lot of doctors are terribly ignorant on these issues. Why have kids suffer because of that?

My oldest daughter finally just made all her kids gluten-free, and couldn't care less what any doctor says. Her kids feel better, that's all that counts. Please do your children a favour, and do the same.

Way to go Ursa... my opinion exactly.

I would just like to add, that if you have celiac & know how well that you feel on the diet & you know what made you sick - how can you feed it to your children?!! I just do not get this. It is like we have to line up like robots & wait for the doctors to tell us something that we already know. You should hear some of the people rant that almost lost their children - they were literally in the hospital at deaths door - the parents will not now touch wheat... & you should hear the idiot doctor advisor to our support group argue with them that a gluten-free diet is not necessary for them! We all thought the doctor was nuts...

How are the parents going to feel if the children get diabetes or cancer or something else before they test positive for celiac????????

Owen'sMom Rookie

The german GI now thinks he might have fructose malabsorption so they want him on a fructose free diet. This is were we are at right now with the testing.

I would like to know what exactly we are all dealing with, Owen had improved on the gluten free diet but wasn't perfect either, hence the reasoning we are still trying to figure things out.

So hopefully with a scope we'll have more answers.

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. - tiffanygosci replied to tiffanygosci's topic in Introduce Yourself / Share Stuff
      1

      Celiac support is hard to find

    2. - trents replied to mamaof7's topic in Parents, Friends and Loved Ones of Celiacs
      1

      Help understand results

    3. - mamaof7 posted a topic in Parents, Friends and Loved Ones of Celiacs
      1

      Help understand results

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

      Newly diagnosed mam to coeliac 11 year old

    5. - tiffanygosci posted a topic in Introduce Yourself / Share Stuff
      1

      Celiac support is hard to find

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

    • Total Members
      132,956
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • tiffanygosci
      EDIT: I did find a monthly Zoom meeting for Celiacs through the Celiac Disease Foundation, so I'll be able to talk with some other people on January 15. And I also found a Celiac Living podcast on Spotify made by a celiac. I feel a little bit better now and I am still hoping I will find some more personal connections in my area.
    • trents
      Welcome to the celiac.com community, @mamaof7! It means for the one celiac disease antibody test that was ordered, she tested negative. However, other tests should have been ordered, especially for someone so young who would have an immature immune system where there would be a high probability of being IGA deficient.  The one test that was ordered was an IGA-based antibody test. It is not the only IGA antibody test for celiac disease that can be run. The most common one ordered by physicians is the TTG-IGA. Whenever IGA antibody tests are ordered, a "total IGA" test should be included to check for IGA deficiency. In the case of IGA deficiency, all other IGA tests results will be inaccurate. There is another category of celiac disease antibody tests that can be used in the case of IGA deficiency. They are known as IGG tests. I will attach an article that gives an overview of celiac disease antibody tests. All this to say, I would not trust the results of the testing you have had done and I would not rule out your daughter having celiac disease. I would seek further testing at some point but it would require your daughter to have been eating normal amounts of gluten for weeks/months in order for the testing to be valid. It is also possible she does not have celiac disease (aka, "gluten intolerance") but that she has NCGS (Non Celiac Gluten Sensitivity, or just "gluten sensitivity" for short) which is more common. The difference is that celiac disease is an autoimmune disorder that damages the lining of the small bowel whereas NCGS does not autoimmune in nature and does not damage the lining of the small bowel, though the two conditions share many of the same symptoms. We have testing to diagnose celiac disease but there are no tests for NCGS. To arrive at a diagnosis of NCGS, celiac disease must first be ruled out. A gluten free diet is the solution to both maladies.   
    • mamaof7
      For reference, daughter is 18 mths old. Was having painful severe constipation with pale stool and blood also bloating (tight extended belly.) Liver and gallbladder are normal. Ultrasound was normal. Dr ordered celiac blood test. We took her off gluten after blood draw. She is sleeping better, no longer bloated and stools are still off color but not painful.    "GLIADIN (DEAMID) AB, IGA FLU Value  0.84 Reference Range: 0.00-4.99 No further celiac disease serology testing to be performed. INTERPRETIVE INFORMATION: Deamidated Gliadin Peptide (DGP) Ab, IgA A positive deamidated gliadin (DGP) IgA antibody result is associated with celiac disease but is not to be used as an initial screening test due to its low specificity and only occasional positivity in celiac disease patients who are negative for tissue transglutaminase (tTG) IgA antibody."   Anyone know what in the world this means. She isn't scheduled to see GI until late April. 
    • 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.
×
×
  • 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.