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

Undigested Food


crittermom

Recommended Posts

crittermom Enthusiast

So I have been watching Michael's bms and they have not turned white or gray like Katharine's did but I have been noticing that his food is coming through more and more undigested! He had French Fries today and at just over 1 hour he had bm and the french fries came out exactly how they went in. There was even one that he swallowed half of whole and the reason I know this is because there it was the same on the other end! (sorry to be gross) He is not potty trained yet which in a way I guess is good because I can see the bm up close and personal. I have noticed lately that his blueberries, crackers, carrots, potatoes, amonst others, even banana is coming out undigested. Along with the fecal matter there are extremely large recognizable chucks of food in there. I am taking him for his second blood panel that the doctor ordered tomorrow and I have a call into the GI. If these tests come back negative and they "just want to wait to do another test" I think I am going to just take him gluten free and I will deal with the schools and his questions when the time comes. There is just something not right. Oh and he is still pooping 4-6 times per day with eating very little and they are still green! I can't believe any of this is normal, Any thoughts?.....


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



Celiac.com Sponsor (A8-M):



Ursa Major Collaborator

From what you are saying, you really know, deep down, that Michael has celiac disease as well. Infant reflux is a common symptom of celiac disease, too.

I would take him off gluten as soon as his blood has been taken and forget about the GI. You really don't want to wait until he gets really ill and stops growing! And with his food not digesting, it is just a matter of time until that happens.

Owen'sMom Rookie

When my son was eating gluten he had lots of undigested foods in his diaper. Sometimes it was nothing but undigested food and some mucous.

Now that he is gluten free again, his stools don't have nearly as much undigested foods in them as before.

He also has other food intolerances and whenever he eats something that doesn't agree with him, he gets loads of undigested foods not even an hour later in his stools.

I agree after the blood panel to go gluten free and see if it helps. My son had the bloodwork and biopsy done and both came back negative. His gene testing results are in my sigline, and we have him gluten free and he has been doing so much better.

todzwife Rookie

This is VERY interesting to me because DD has the SAME Thing. She was recently diagnosed as having a sever wheat allergy (via the RAST test) but I have not had her tested for celiac. I'm really wondering if I should.

I see a LOT of food come through completely intact (including french fries as mentioned above) carrots, beans, and even wild rice.

She is a very predictable pooper (usually twice a day, once in the AM and once before bed after her bath LOL!) and is not potty trained so I too get a birds eye view of her lovelies.

After reading here for awhile, I am becoming more and more concerned that it is not just a wheat allergy but is actually celiac. She has SO many symptoms that have been noted here including dry patchy skin, undigested and unformed bowel movements, irritability, infant reflux, poor sleep habits...the list goes on.

Is the enterolab (I know I'm spelling that wrong) gluten sensitivity test enough to "diagnose" her?

Gilli's mother Newbie

After I found out that my daughter had Celiac (age 2) I started giving her probiotics and enzymes and saw a huge difference in her bowel movements. I opened a capsule, mixed it in juice or goat's milk (she can't tolerate cow's milk) in a shot glass to be sure she finished it all. Do this before any meal and you will notice a big difference in days. I give her the probiotics at bedtime in the same manner. Be sure it is in a capsule - powder form so that you can mix it with a beverage or mix in a goat yogurt. After you start this and the bm's become more formed it should be easier for you to find out what other foods your son might be sesitive to. If it was only celiac like I believed early on it would have been so simple but we found out that pastuerized cow's dairy, soy, nuts, dyes, nitrates, too much rice and many oils also caused my daughter to react and the bowel movements always confirmed it. We also healed her esophagus by giving her the probiotics, enzymes, primrose oil and capsules of colostrum. I know this because she had a scope a year after her first (scope) and her GI was completely amazed. The celiac diet is exhausting at first (and in the winter) but you will get the hang of it and it only gets easier - especially if you have a good health food store in town! I believe it is better to assume that your child has celiac and feed accordingly than to drive yourself crazy with the testing! It can't hurt to be on a gluten free diet and you can get your answer quickly by the change in behavior, bowel movements and their quality of sleep. Sorry so long!

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. - Heatherisle replied to Mihai's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      22

      Pain in the right side of abdomen

    2. - Heatherisle replied to Mihai's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      22

      Pain in the right side of abdomen

    3. - Scott Adams replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      how long does it take for the genetic blood test for celiac to come back?

    4. - knitty kitty replied to Mihai's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      22

      Pain in the right side of abdomen

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

    • Total Members
      133,667
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • Heatherisle
      Hasn’t been given folic acid as GP says vit b and folic acid can’t be given together which I find strange cos any time I did venepunctures B12 and folate were always grouped together? Her folate level was 2.2, just below the normal level
    • Heatherisle
      Hi Thanks for your input. Don’t know which exact medication she’s on, keep asking but she keeps forgetting!!! I still think her Vitamin D levels might be low cos she had the back pain and tingling last year( around March /April) and levels were low so she had 3 month course then and it helped. She’s coming home next week (as in to ours) for a long weekend so hopefully some TLC from mum and dad will help!!!    
    • Scott Adams
      Genetic testing for celiac disease (the HLA-DQ2 and HLA-DQ8 genes) usually takes about 3–10 days to come back, depending on the lab your doctor uses, though some places may take up to two weeks. The test itself doesn’t diagnose celiac disease—it only shows whether you carry the genes that make celiac possible. About 30–40% of people have one of these genes, but only a small percentage actually develop celiac disease. However, if the test is negative for both genes, celiac disease becomes extremely unlikely, which is why your doctor mentioned possibly canceling the endoscopy if the result is negative. If it’s positive, it just means celiac remains a possibility and further testing, like a gluten challenge followed by endoscopy, helps confirm it. Since you have an identical twin, it’s definitely useful information to share if the genes are present, because twins share the same genetic risk. It sounds like you found a very thorough GI doctor, which is great, especially since she’s also monitoring nutrients and looking at the whole picture.
    • knitty kitty
      @Heatherisle, You're not a bother at all.   What "Vitamin B medication" is she taking?  Is it just B12 and folate?   All eight B vitamins, Vitamin D and other vitamins and minerals need to be supplemented because the malabsorption of Celiac disease affects all the nutrients.  All the B vitamins work together.  Just supplementing one or two can throw the other B vitamins out of balance causing worsening deficiencies in other B vitamins.  Doctors are undereducated about nutrition.  Heavy sigh. This is worrisome.  These are all symptoms of Gastrointestinal Beriberi caused by Thiamine deficiency.   An Erythrocyte Transketolace Activity Assay needs too be done to check her Thiamine level.  But because this test is so expensive and takes so long for the results to come back, it's much simpler to administer 500 mg Thiamine Hydrochloride several times a day for several days and look for health improvement (WHO recommendation).  Doctors can administer Thiamine Hydrochloride by IV along with a "banana bag" with all the B vitamins in it.  (Riboflavin gives it the yellow color.).  I've experienced vitamin deficiencies which my doctors didn't recognize.  When thiamine and B12 deficiencies started affecting my brain function, my doctors wrote me off as a depressed hypochondriac.  I had Gastrointestinal Beriberi myself.  I took over the counter thiamine hydrochloride at home and had health improvement within an hour.  High doses (500 mg) of Thiamine are needed to "jump start" the body into proper functioning.   Apologies if I was curt.  I get very frustrated because the nutritional deficiencies that occur with Celiac disease are not addressed properly.  All I can do is tell people about what I learned on my Celiac journey.  Have you visited my blog?  Tap on my name, look for pull down menu Activities and go to blog.   I do hope your daughter can get the nutritional support she needs.  I'm very worried.  Please keep us updated!
    • Heatherisle
      Hi  Thank you, will tell her to do that
×
×
  • 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.