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

Wondering If My Son Has Celiac Disease?


KaidensMummy

Recommended Posts

KaidensMummy Rookie

I am new to this board & was wondering if someone could help out with some advice.

I have been so frustrated because I feel the doctor is not doing enough.

My son just turned 2 yrs old & has diarrhea everyday.

When my son was a baby on formula the doctor said that he was lactose intolerant as he was crying, bloating, diarrhea. We then took him off of regular formula & switched to soy formula & everything seemed to be much better.

Since my son has been eating he has had diarrhea.

The diarrhea is VERY smelly & is sometimes mucusy(sp), slimy, oily with food that is undigested a lot of times. We have gone to the doctor MANY times asking him what the problem could be. I have asked if I should quit giving him any dairy products, he told me not to do that.

He has told me to try the BRAT diet which I have & it seemed to help but he said this was a temporary fix basically as he was thinking at the time that he had some sort of bacterial infection.

The doctor also ran a test for low iron as my son was ill a lot last winter with all sorts of things like Bronchitis, croup, strep, eye & ear infections etc. & the test turned back fine.

The only thing we know is he has in asthma & lactose intolerance.

2 weeks ago we went to the doctor again because my son had diarrhea again but this time he had these things in it, for 2 days when he had a BM his BM;s were full of these little clear gel liquid filled things....smaller than the size of a pea. Then he woke up on the 2nd day & vomitted up a bit of food & also these gel things.....so i actually picked these gel looking things up & put them in a clear baggy & took them to the drs. office. The doc said he had no clue what this was & wanted me to take stool samples & send them in to the lab.

the doctor says the test say my son is fine.

I have no clue what to do now & am pulling out hair as to what I should be doing.

My son is having this diarrhea everyday & it seems to happen shortly after eating & his diaper is full right away & sometimes even leaks.

Does this sound like Celiac disease as this seems to be the only thing I could think it may be???

Thanks for your help.


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



Celiac.com Sponsor (A8-M):



Mother of Jibril Enthusiast

It's difficult to get an accurate result from testing for celiac in such a small child. The best thing is simply to take suspicious food(s) out of your son's diet and see if it makes a difference. Gluten is a great place to start. So is dairy! There's nothing unhealthy about this kind of diet. My nine-month-old son is intolerant to casein (dairy proteins) and corn... maybe gluten too, but at this point I'm not willing to give it a try. Even a tiny amount of dairy or corn gives him diarrhea and terrible eczema on his face :( So... he eats a lot of rice and vegetables with a little meat (he doesn't like fruit very much) and I just started giving him a little soy yogurt with active cultures. He's doing GREAT.

The crying, bloating, and gas is very familiar! My guess is that the "gel" things are undigested fat. That's a common thing to see in the stools of people with food intolerance problems. Since you've ruled out a lot of other things, I would give the gluten-free, dairy-free diet a try.

KaidensMummy Rookie

Thanks so much for that advice...I feel strangely relieved knowing that you & others Im sure know what this is all about.

It has been so frustrating not knowing what to do & not really getting any help from the doctor.

I will now looking into trying a gluten & dairy free diet. I am suspecting that this is not going to be easy so I will need to start checking out this site & figuring out what a gluten & dairy free diet is as I have NO clue where to start.

Again I thank you for your advice & I will get down to the business of reading ;)

Mother of Jibril Enthusiast
Thanks so much for that advice...I feel strangely relieved knowing that you & others Im sure know what this is all about.

It has been so frustrating not knowing what to do & not really getting any help from the doctor.

I know what you mean. I figured out the casein intolerance on my own... my son had colic, diarrhea, lots of sinus congestion, projectile vomiting, and streaks of blood in his diapers... all from the casein getting through my breast milk. I found some good information at www.kellymom.com. He started to improve within a week after I stopped eating dairy. Within six weeks he was back to normal. His pediatrician was completely unhelpful. She wasn't opposed to the idea of changing his diet... she just didn't know much and was skeptical that it would make a difference.

Finding this forum has been a big relief. It's nice to feel understood and have a place to talk about these issues :) Plus I've learned SO much... not just about gluten, but about food intolerance and autoimmune disorders in general.

Incidentally, the Gluten-free Casein-free diet is recommended for kids with autism... not that your son has it! But if you're looking for gluten-free/dairy-free recipes for kids, those are good sites to look at. Another good idea is to post a list of your son's favorite foods on a new thread. People would be happy to help you find substitutions. :P

KaidensMummy Rookie
I know what you mean. I figured out the casein intolerance on my own... my son had colic, diarrhea, lots of sinus congestion, projectile vomiting, and streaks of blood in his diapers... all from the casein getting through my breast milk. I found some good information at www.kellymom.com. He started to improve within a week after I stopped eating dairy. Within six weeks he was back to normal. His pediatrician was completely unhelpful. She wasn't opposed to the idea of changing his diet... she just didn't know much and was skeptical that it would make a difference.

Finding this forum has been a big relief. It's nice to feel understood and have a place to talk about these issues :) Plus I've learned SO much... not just about gluten, but about food intolerance and autoimmune disorders in general.

Incidentally, the Gluten-free Casein-free diet is recommended for kids with autism... not that your son has it! But if you're looking for gluten-free/dairy-free recipes for kids, those are good sites to look at. Another good idea is to post a list of your son's favorite foods on a new thread. People would be happy to help you find substitutions. :P

Thanks for all the tips :) I REALLY appreciate it. It's all so overwhelming

  • 2 weeks later...
boobybabs Rookie

In reference to "wondering if my son has celiac disease" - not sure if this helps, but if you rule out celiac, you might want to research other diseases......a few months ago, I was watching a TV series called "Mystery diagnosis", and there was a family on there whose daughter had years of diarrhea - every time they went to the doctor, they were told that it was nothing serious - ex..would grow out of it, etc.....she continued to experience these problems for several years - eventually when their daughter was older, she was diagnosised with a specific disease....unfortunately, cannot remember more details....maybe they have a website - I do not believe the diagnosis was life threatening....just so that you don't worry about that - In many episodes of this program - people can go from doctor to doctor and remain undiagnosed......In a lot of cases, the diseases are rare and many doctors do not have the knowledge of them..........hope it helps you

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,210
    • Most Online (within 30 mins)
      7,748

    BJ OConnor
    Newest Member
    BJ OConnor
    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

    • trents
      NCGS does not cause damage to the small bowel villi so, if indeed you were not skimping on gluten when you had the antibody blood testing done, it is likely you have celiac disease.
    • Scott Adams
      I will assume you did the gluten challenge properly and were eating a lot of gluten daily for 6-8 weeks before your test, but if not, that could be the issue. You can still have celiac disease with negative blood test results, although it's not as common:  Clinical and genetic profile of patients with seronegative coeliac disease: the natural history and response to gluten-free diet: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5606118/  Seronegative Celiac Disease - A Challenging Case: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9441776/  Enteropathies with villous atrophy but negative coeliac serology in adults: current issues: https://pubmed.ncbi.nlm.nih.gov/34764141/  Approximately 10x more people have non-celiac gluten sensitivity than have celiac disease, but there isn’t yet a test for NCGS. If your symptoms go away on a gluten-free diet it would likely signal NCGS.
    • Xravith
      I'm very confused... My blood test came out negative, I checked all antibodies. I suppose my Total IgA levels are normal (132 mg/dl), so the test should be reliable. Still, I'm not relieved as I can't tolerate even a single biscuit. I need to talk to my doctor about whether a duodenal biopsy is necessary. But it is really possible to have intestinal damage despite having a seronegative results? I have really strong symptoms, and I don't want to keep skipping university lectures or being bedridden at home.
    • Scott Adams
      They may want to also eliminate other possible causes for your symptoms/issues and are doing additional tests.  Here is info about blood tests for celiac disease--if positive an endoscopy where biopsies of your intestinal villi are taken to confirm is the typical follow up.    
    • Scott Adams
      In the Europe the new protocol for making a celiac disease diagnosis in children is if their tTg-IgA (tissue transglutaminase IgA) levels are 10 times or above the positive level for celiac disease--and you are above that level. According to the latest research, if the blood test results are at certain high levels that range between 5-10 times the reference range for a positive celiac disease diagnosis, it may not be necessary to confirm the results using an endoscopy/biopsy: Blood Test Alone Can Diagnose Celiac Disease in Most Children and Adults TGA-IgA at or Above Five Times Normal Limit in Kids Indicates Celiac Disease in Nearly All Cases No More Biopsies to Diagnose Celiac Disease in Children! May I ask why you've had so many past tTg-IgA tests done, and many of them seem to have been done 3 times during short time intervals?    
×
×
  • 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.