Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

My 4-year Old's Symptoms - Need Advice


GraceE

Recommended Posts

GraceE Rookie

Hello there! I have several postings myself out there about my own suspected celiac/gluten intolerance. I'm also curious about my 4 year old daughter. She's struggled from the day she came into this world with massive reflux as an infant and continuous constipation. She STILL has constipation. Recently she was complaining multiple times a day that her tummy hurt. No diahrea (sp?) or vomiting, though. I took her to the dr. a few months ago and they think the tummy ache complaints are from all the constipation, which could be true. She's been off and on Miralax for years. She also complains pretty frequenty of headaches.

I've tried to stress the importance of only telling me that her tummy hurts if it really does...you know how kids can get in those habits of saying stuff like that. She's definitely not underweight - she's actually always been in aobut the 90th percentile for weight at 75th for height. She wants to eat all the time!! I swear the kid eats more than me! She has a big belly but I've always attributed it to just her big appetite. It's not hard, but just big! I have to buy her clothes a size too big just to make room for her gut!

It just hit me the other day, with all of my GI issues, diagnosed severe IBS and my personal suspicions of celiac or gluten intolerance that maybe this is her problem too?

She's never been a really active child...gets pretty worn out quickly. She was also a late crawler (1 year old) and didn't walk until she was 18 months. But academically she's wonderful - ahead of her age.

Does anyone have any suggestions? I love her pediatrician but I'm afraid she'll brush it off again. She thinks the constipation is just a fact of life and probably a result of what 4 year olds like to eat. But this has been going on since day one. And I really try to limit sweets and as much unhealthy food as I can. She probably only poops twice a week. And when she does it's a bowl full!!

Last thing....she doesn't get sick very often. Just this nagging complaint of headache and tummy ache. Plus the constipation.

Anyone have any thoughts?


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



Celiac.com Sponsor (A8-M):



Jestgar Rising Star

Just try her gluten free. If it makes a difference you'll have one more piece of ammo for the ped.

dionnek Enthusiast

That sounds a lot like my daughter (who is just 2 1/2 now). She had vomitting/acid reflux from the time she was born until about 1 year old, when we finally went to a new dr. who put her on acid reflux meds and that helped, but since the age of 18 months she's had constipation (now on Mirilax too which helps). Anyway, when I was dx recently I had her genetically tested and she has one of the genes. Her ped now says the enamel on her teeth is wearing away, so he wants to do the blood test. I would suggest getting your daughter genetically tested (we used Enterolab - insurance did not pay) and if she has the gene, then you should probably either get her blood tested or just do the diet. But, if you are going to do the diet yoiu will not be able to get her blood tested without going back on gluten. It's not that easy to just do the diet, especially for a toddler who is probably in school or about to go to school - you would have to make sure she doesn't get any cross contamination at school, etc., but that is a personal decision. Lots of people don't bother with the tests and just try the diet, but you have to be strict for it to work (and it might take awhile - took me 7 plus months before I noticed a difference and I'm still not 100% by any means!). Good luck!

GraceE Rookie
That sounds a lot like my daughter (who is just 2 1/2 now). She had vomitting/acid reflux from the time she was born until about 1 year old, when we finally went to a new dr. who put her on acid reflux meds and that helped, but since the age of 18 months she's had constipation (now on Mirilax too which helps). Anyway, when I was dx recently I had her genetically tested and she has one of the genes. Her ped now says the enamel on her teeth is wearing away, so he wants to do the blood test. I would suggest getting your daughter genetically tested (we used Enterolab - insurance did not pay) and if she has the gene, then you should probably either get her blood tested or just do the diet. But, if you are going to do the diet yoiu will not be able to get her blood tested without going back on gluten. It's not that easy to just do the diet, especially for a toddler who is probably in school or about to go to school - you would have to make sure she doesn't get any cross contamination at school, etc., but that is a personal decision. Lots of people don't bother with the tests and just try the diet, but you have to be strict for it to work (and it might take awhile - took me 7 plus months before I noticed a difference and I'm still not 100% by any means!). Good luck!

Thank you for the advice! I have a quick question about Enterolab. I've heard a lot of controversy out there about that. I've also hear that about 99% of doctors don't consider those results accurate. Any thoughts on that? Thanks!

Nic Collaborator

Hi, I had the same problem wilth my son who is now 6. He would projectile vomit as an infant and nearly hit people across the room :P . Then as he approached 1 year the constipation started. It has never stopped. By 4 they put him on Miralax daily which he still takes everyday. Later that year he was diagnosed Celiac and he has been gluten free ever since. I would like to say that the constipation went away quickly but it did not. He still suffer terribly even on the Miralax and just went through a colonoscopy to determine why he is in constant discomfort and why he cannot poop even soft poop without a struggle. He even had to struggle to poop during the "cleaning out" for the colonoscopy, it was all water, and still he had to struggle. They believe they saw signs of another food intolerance while in there but we are still waiting for the biopsy results. I am telling you this because my old ped. GI kept saying Jacob was just constipated and we need to get him on a better pooping schedule but that does not seem to be it. We now face another possible intolerance and all the while I have been waiting for his symptoms to go away. I would suggest once your child is gluten free for 6 months, if you don't see significant improvement, then look farther. Hopefully the constipation will just go away with the gluten free diet.

Nicole

Suzie-GFfamily Apprentice

My daughter (now age 6) had a lot of reflux as a baby and constipation that started sometime about age 1 and didn't stop. I would mention her constipation (plus the bumpy skin on her legs) at her annual check-ups and asked whether it could be a food intolerance... I suspected that maybe it was dairy.

Last year I read about celiac disease- I actually didn't think that my daughter had it at first because she had "mild" complaints and some of the symptoms I read about sounded "severe". My mom was really sick last year- and I first suspected that my mom was celiac. Turns out she was- plus me and my daughter and my son.

When I asked my daughter's doctor to do a blood test she seemed surprised, but luckily ordered the test. My daughter's TTG levels were exceptionally high. She does have celiac disease.

Suzie

dionnek Enthusiast

I have heard that a lot of dr's don't recognize Enterolab, but I did a lot of asking around and the only 2 labs I found that would do the genetic testing was Enterolab and Kimball, and Enterolab was a little cheaper (for just the genetic - I didn't get any other tests done). I didn't really care if a dr. accepted it or not b/c I just wanted to know for my own piece of mind (to know if I had to worry about it at all in the future or not). I think dr's just don't like what they don't know ;)


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.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,164
    • Most Online (within 30 mins)
      7,748

    VGL
    Newest Member
    VGL
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):




  • Who's Online (See full list)


  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • DAR girl
      Looking for help sourcing gluten-free products that do not contain potato or corn derived ingredients. I have other autoimmune conditions (Psoriatic Arthritis and Sjogrens) so I’m looking for prepared foods as I have fatigue and cannot devote a lot of time to baking my own treats. 
    • Scott Adams
      I am so sorry you're going through this. It's completely understandable to feel frustrated, stressed, and disregarded after such a long and difficult health journey. It's exhausting to constantly advocate for yourself, especially when you're dealing with so many symptoms and positive diagnoses like SIBO, while still feeling unwell. The fact that you have been diligently following the diet without relief is a clear sign that something else is going on, and your doctors should be investigating other causes or complications, not dismissing your very real suffering. 
    • Oldturdle
      It is just so sad that health care in the United States has come to this.  Health insurance should be available to everyone, not just the healthy or the rich.  My heart goes out to you.  I would not hesitate to have the test and pay for it myself.  My big concern would be how you could keep the results truly private.  I am sure that ultimately, you could not.  A.I. is getting more and more pervasive, and all data is available somewhere.  I don't know if you could give a fake name, or pay for your test with cash.  I certainly would not disclose any positive results on a private insurance application.  As I understand it, for an official diagnosis, an MD needs to review your labs and make the call.  If you end up in the ER, or some other situation, just request a gluten free diet, and say it is because you feel better when you don't eat gluten.      Hang in there, though.  Medicare is not that far away for you, and it will remove a lot of stress from your health care concerns.  You will even be able to "come out of the closet" about being Celiac!
    • plumbago
      Yes, I've posted a few times about two companies: Request a Test and Ulta Labs. Also, pretty much we can all request any test we want (with the possible exception of the N protein Covid test and I'm sure a couple of others) with Lab Corp (or Pixel by Lab Corp) and Quest. I much prefer Lab Corp for their professionalism, ease of service and having it together administratively, at least in DC. And just so you know, Request a Test uses Lab Corp and Quest anyway, while Ulta Labs uses only Quest. Ulta Labs is cheaper than Request a Test, but I am tired of dealing with Quest, so I don't use them so much.
    • Scott Adams
      PS - I think you meant this site, but I don't believe it has been updated in years: http://glutenfreedrugs.com/ so it is best to use: You can search this site for prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
×
×
  • Create New...