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

Strange Stools


kim26

Recommended Posts

kim26 Apprentice

hi everyone,

my daughter was recently diagnosed, and doing sooo much better! my question today is about my 4 year old son. he's been having green and orange stools, sometimes normal in consistency, sometimes loose but not what i would call diarrhea, and lately some pellet like stool mixed in.....almost always green and orange in color, his appetite has definitely decreased and he complains of tummy aches at least once a day. this has been going on for a while but has gotten worse in the past 2 months. his pcp ordered a celiac panel and we had his blood taken today so we will see what the results are soon, hopefully...although i know they aren't hugely reliable in young children. does this sound familiar to anyone, or does anyone know if this has anything to do with celiac? or something entirely different? these symptoms are different than my daughter's so im just not sure. any help would be appreciated.... thx ~K


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



Celiac.com Sponsor (A8-M):



shayesmom Rookie
my question today is about my 4 year old son. he's been having green and orange stools, sometimes normal in consistency, sometimes loose but not what i would call diarrhea, and lately some pellet like stool mixed in.....almost always green and orange in color, his appetite has definitely decreased and he complains of tummy aches at least once a day. this has been going on for a while but has gotten worse in the past 2 months. his pcp ordered a celiac panel and we had his blood taken today so we will see what the results are soon, hopefully...although i know they aren't hugely reliable in young children. does this sound familiar to anyone, or does anyone know if this has anything to do with celiac? or something entirely different? these symptoms are different than my daughter's so im just not sure. any help would be appreciated.... thx ~K

It has been my experience wth my dd that different colored/textured stools are often due to a food allergen or intolerance going on. For my dd, dairy gives yellowish stools, soy and egg give orange stools, gluten gives a clay colored one. Food colorings or artificial sweeteners give the pellet-like stool. (How sad is it that I've recognized what goes with what???).

Hopefully testing will help determine some of what is behind this. Otherwise, I would keep a food journal and start keeping track of what went in and what came out.

Also, I've found this site to be helpful in explaining some of what you've described: Open Original Shared Link

feedmykids Rookie

It's a strange question to ask but - Do his Poops float? That is a sign tht he is not digesting his fats. My DN has Cystic Fibrosis and that it if how they found out is that she had orange greasy poop that floated, and got tested for it. There is such a similarity between cystic fibrosis and celiac. The doctors at our childrens hospital say the only real big difference is the salt the body makes. If he tastes salty or his poop floats get him tested for Cystic fibrosis too.

RiceGuy Collaborator

Given the unreliability of the tests for young children, and you've already gotten the blood work ordered, I'd be inclined to put him an a gluten-free diet even before the blood test results are in. That would be far more accurate anyway.

kim26 Apprentice

thanks everyone for the replies! i have considered putting him on the gluten-free diet since my daughter and i are on it anyway(i tested negative for celiac, but have been "diagnosed" with IBS and duodenitis and hypothyroidism), but he is a very picky eater and i think i would have a hard time keeping him on it unless i know in my own head its necessary. he was a preemie by just a few weeks and his stay in the nicu broke my heart so im the first to admit that im a bit a of a sucker when it comes to giving in to him lol! i am just wondering if i should even be worried, sometimes his poop is normal, and im not sure if it floats....i think I've been so distracted by the color i haven't paid attention to much else lol any suggestions or helpful hints, things to look into would be helpful in addition to the replies I've already gotten :-)~K

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,207
    • Most Online (within 30 mins)
      7,748

    WAB19
    Newest Member
    WAB19
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

  • 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.