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

Implications of Diarrhea In Person With celiac disease on gluten-free Diet


plumbago

Recommended Posts

plumbago Experienced

If after having been gluten-free for several years, you get D after ingesting gluten, does that mean you have an unhealed gut? In other words, what is the pathogenesis of the D reaction in celiac disease – or better put: is D only a symptom of celiac disease when the villi are flattened? If true, that means after 6 years of being 99.5% compliant, my villi still are not healed!!!???

As Peter Greene says, “The system’s first line of defense is an intact mucosa [small intestines].”

Plumbago


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



Celiac.com Sponsor (A8-M):



GFinDC Veteran
1 hour ago, plumbago said:

If after having been gluten-free for several years, you get D after ingesting gluten, does that mean you have an unhealed gut? In other words, what is the pathogenesis of the D reaction in celiac disease – or better put: is D only a symptom of celiac disease when the villi are flattened? If true, that means after 6 years of being 99.5% compliant, my villi still are not healed!!!???

As Peter Greene says, “The system’s first line of defense is an intact mucosa [small intestines].”

 

Plumbago

Hi plumbago,

No, D is not a symptoms only associated with severe celiac disease damage, if that's what you are thinking.  Every time we ingest gluten the immune reaction is kicked off again, and the damage starts all over.  If we ingest gluten daily, the immune reaction never stops, and we end up  with significant damage.  If we stop eating gluten, the immune reaction will decrease over time, and the damage will decrease also.  Healing will also happen as well.

The moral of the story is Stop Eating Gluten! :D

plumbago Experienced

Thank you for responding. Yes, I understand not to eat gluten.

I suppose, I wasn’t clear. I understand that there are reasons for D other than celiac disease. What I am asking is, within the context of celiac disease, is there another reason apart from villi blunting for D? My suspicion is there is not. In which case, if, after being gluten-free for six years, I get D when I accidentally ingest gluten, it is likely a sign that my SI/duodenum has not healed, which would be a major bummer. That’s basically the gyst of and background for my question.

GFinDC Veteran
On 10/22/2016 at 4:25 PM, plumbago said:

Thank you for responding. Yes, I understand not to eat gluten.

I suppose, I wasn’t clear. I understand that there are reasons for D other than celiac disease. What I am asking is, within the context of celiac disease, is there another reason apart from villi blunting for D? My suspicion is there is not. In which case, if, after being gluten-free for six years, I get D when I accidentally ingest gluten, it is likely a sign that my SI/duodenum has not healed, which would be a major bummer. That’s basically the gyst of and background for my question.

Hmm, we may be talking in circles a bit.  My take on your words in red is that you think having D when glutened 1) means you your villi never healed even though you were gluten-free for years?  Or do you mean, 2) your villi healed, and you ate gluten, and then the new damage from the recent glutening caused villi damage and D?

#2 gets my vote.  Anytime we ingest gluten the immune system kicks in and starts "protecting" us.  That protection includes attacking and damaging the gut llning where the nasty gluten is hiding.  That can cause D.  The D doesn't mean you never healed, but that you got new, recent damage.  The celiac disease reaction is not forgotten by the immune system.  The immune system always knows how to fight the gluten threat.  But our bodies do know how to heal also.  Our guts are continually rebuilding the gut lining even in non-celiacs.  The gut takes a lot of damage from just plain digesting food.  Add in the immune system attack the healing process can get left behind  in the dust.

cyclinglady Grand Master

There really aren't many studies done that follow Celiacs and their levels of healing.  Here is an article about a study that I once saw (but can not locate at the moment):

Open Original Shared Link

As far as diarrhea, being a sign of damaged villi, I can only speak for myself.  I had flattened villi (patches) and I had no diarrhea, but only anemia (little did I know of the bone damage).  I have had follow-up blood work, but no biopsies.  Healed or not my symptoms improve by maintaining a gluten-free diet. 

RMJ Mentor

I think this is the journal article:

Open Original Shared Link

plumbago Experienced

Yes, GFinDC you've got the gyst of what I am after. If I am reading your response correctly then, you think that inflammation in the gut caused by gluten ingestion is enough to trigger diarrhea, quite apart from the state of one's mucosa? That would be good news for me. More information on this inflammation reaction in the gut with gluten ingestion is precisely what I am after, but cannot seem to find. Because, as stated, as far as I know, D is mostly if not only, caused by flattened villi.

OTOH, how interesting to hear from you, cycling lady, that you had flattened villi and no D!

RMI, the link is quite depressing. Many appear not to have healed mucosas after a gluten-free diet. A repeat endoscopy is what is so clearly needed by many of us, but honestly I am a little wary of the risks.


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



Celiac.com Sponsor (A8-M):



plumbago Experienced

UPDATE: 

So as I have said, I was worried that my occasional D was indicative of an unhealed gut/small intestine/duodenum. I thought and thought about this. If my gut were really unhealed, wouldn’t I be having a lot more that occasional diarrhea?  I think I would be.

So now I’m thinking that the diarrhea may be a result of IBS. Here's why: it seems the more I’m sitting at home, ie on the weekends, sitting and eating, the greater the frequency of stools, and the fattier they get with each BM. Whereas, during the weak, I eat (less), get up and go to work, don’t eat as much while I am at work and don’t have BMs, and if I do, they are not fatty - and I do not have D. All of which is to say that I think it's possible that the fattiness is caused by the increased transit time of IBS, leading to more water in the stool,  less time for the fat and water to be absorbed.

Now, what is causing the IBS? (First of all, the medical line is, no one knows.) I am fairly certain I am not getting glutened. However, on the weekends, I will eat a high fiber, high protein meal followed by hours of sitting, consuming coffee with milk and sugar. I think the problem or the issue lies in what I am consuming. I tend to think the culprit is the milk. (The coffee is not always caffeinated.) 

 

Edit to add: Now I'm reading that most floating stools are not caused by an increased fat content - not to say the floating stool is free of fat, but from what I'm reading, the cause for floating is gas.

 

"Most floating stools are not caused by an increase in the fat content of the stool. However, in some conditions such as chronic pancreatitis, the fat content is increased." Open Original Shared Link

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. - Scott Adams replied to pothosqueen's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      2

      Positive biopsy

    2. - Scott Adams commented on Scott Adams's article in Latest Research
      3

      New "Glowing Bacteria" Pill Could Transform Gut Disease Detection (+Video)

    3. - trents replied to mamaof7's topic in Parents, Friends and Loved Ones of Celiacs
      7

      Help understand results

    4. - Jordan Carlson posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      0

      Fruits & Veggies

    5. - wellthatsfun posted a topic in Gluten-Free Recipes & Cooking Tips
      0

      heaps of hope!

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

    • Total Members
      132,998
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • Scott Adams
      If you are still eating gluten you could get a celiac disease blood panel done, but I agree with @trents and the gold standard for diagnosing celiac disease would be your endoscopy results. Is it possible they did do a celiac disease panel before your biopsy? This would be the normal chain of events. This article might be helpful. It breaks down each type of test, and what a positive results means in terms of the probability that you might have celiac disease. One test that always needs to be done is the IgA Levels/Deficiency Test (often called "Total IGA") because some people are naturally IGA deficient, and if this is the case, then certain blood tests for celiac disease might be false-negative, and other types of tests need to be done to make an accurate diagnosis. The article includes the "Mayo Clinic Protocol," which is the best overall protocol for results to be ~98% accurate.    
    • trents
      Actually, it would be more correct to say that the genetic potential to develop celiac disease is passed down from parents to children. About 40% of the general population has the genetic potential to develop celiac disease but only about 1% of the general population actually do. But it is also true that the offspring of those who do have active celiac disease are at a considerably higher risk of developing active celiac disease than those of parents who have the genes but don't develop the disease. Some recent, larger studies put the risk at near 50% for the first degree relatives of those who have active celiac disease.
    • Jordan Carlson
      Hello everyone! Been a while since I posted. The past few moths have been the best by for recovery for myself. I have been the least bloated I have ever been, my constant throat clearing is almost gone, I have stopped almost all medication I was prevously taking (was taking vyvanse for adhd, pristiq for anxiety,fomotadine/blexten for histamine blockers and singulair). Only thing I take now is Tecta. I also no longer get any rashes after eating. Things are going very well. Most success came actually once I upped my B12 daily dose to 5,000 mcg. I do have one thing I am un able to figure out and want to see if anyone else has this issue or has experience working around it. Ever since I was born I have always had a issue getting fruits and veggies down. No matter how hard I tried, it would always result in gagging or throwing up. Always just thought I was a picky eater. Now that my stomach and system has healed enough that I can feel when something is off almost istantly, I notice that after eating most fruits (sometimes I am ok with bananas) and veggies, my stomach instantly starts burning and my heart starts to pound and I get really anxious as if my body doesnt know what to do with what just enetered it. So I am thinking now that this is what probably was going on when I was born and my body started rejecting it before which caused this weird sensory issue with it causing the gagging. Hoping someone has some exprience with this as well because I would love to be able to enjoy a nice fruit smoothie once in a while haha. Thanks everyone!
    • wellthatsfun
      i know i've been rather cynical and sad about being fully diagnosed in june 2025, but my boyfriend has been consistently showing me the wonderful world that is gluten free cooking and baking. in the past couple of days he's made me a gluten free rice paper-wrapped spanakopita "pastry", plus a wonderful mac and cheese bechamel-ish sauce with gluten free pasta (san remo brand if you're in australia/if you can get your hands on it wherever you are).  those meals are notably gluten free, but mainly he's been making me easy gluten free meals - chili mince with white rice and sour cream, chicken soup with homemade stock from the chicken remains, and roast chickens with rice flour gravy and roast veggies. i'm a bit too thankful and grateful lol. how lucky could i possibly be? and, of course, for those who don't have someone to cook for them, it's quite easy to learn to cook for yourself. i've been making a lot of meals for us too. honestly, cooking is pretty darn fun! knowing basic knife skills and sanitary practices are all you really need. experimenting with spices will help you get on track to creating some really flavourful and yummy dishes. coeliac is a pain, but you can use it to your advantage. healthier eating and having fun in the kitchen are major upsides. much luck to all of you! let's be healthy!
    • knitty kitty
      That test is saying that your daughter is not making normal amounts of any IGA antibodies.  She's not making normal amounts of antibodies against gliadin, not against bacteria, not against viruses.  She is deficient in total IGA, so the test for antigliadin antibodies is not valid.  The test was a failure.  The test only works if all different kinds of antibodies were being made.  Your daughter is not making all different kinds of antibodies, so the test results are moot.  Your daughter should have the DGP IgG and TTG IgG tests done.   The tests should be performed while she is still consuming gluten.  Stopping and restarting a gluten containing diet can make her more sick, just like you refuse to eat gluten for testing.  Call the doctor's office, request both the IGG tests. Request to be put on the cancellation list for an appointment sooner.  Ask for genetic testing.   Celiac disease is passed on from parents to children.  You and all seven children should be tested for genes for Celiac disease.  Your parents, your siblings and their children should be tested as well.  Eating gluten is not required for genetic testing because your genes don't change.  Genetic testing is not a diagnosis of Celiac disease.  Just having the genes means there is the potential of developing Celiac disease if the Celiac genes are activated.  Genetic testing helps us decide if the Celiac genes are activated when coupled with physical symptoms, antibody testing, and biopsy examination. It's frustrating when doctors get it wrong and we suffer for it.  Hang in there.  You're a good mom for pursuing this!  
×
×
  • 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.