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

Mucousy Stools A Symptom?


stomica

Recommended Posts

stomica Rookie

My daughter who is now 2 1/2 was diagnosed with ulcerative colitis in January after a colonoscopy. Her main symptoms were loose stools (2 x day) with lots of mucous and, infrequently, traces of blood. She's been on the meds for her colitis for two months now, though I don't see any change in her stools. The ped GI tested her stool and found no blood as well as no WBC's, which is a measure of inflammation. He ordered one more test (alpha 1-antitrypsin) to check out the inflammation in the colon as well.

In February, her celiac panel came back positive for IgA's and IgG's, though the other two were negative. He said he wants to recheck that in two more months to see if the numbers have increased. He said we need to give it some time for her to build up antibodies to get an accurate result (since two year olds haven't had much time to do that).

I know her symptoms are mild right now, but I'm having trouble waiting. I just want to fix it! I understand going gluten free would be tough, but I want to do whatever is best for her. Here's my main questions...She's very pale with dark circles under her eyes - is that also pretty common in kids with celiac disease? Also, is mucousy stools a common symptom? It's so hard to say since she was diagnosed with ulcerative colitis as well. Any info would be appreciated! Thanks!


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



Celiac.com Sponsor (A8-M):



gf4life Enthusiast

Have you and your doctor conscidered gene testing? Both the dark circles and the mucousy stool could be caused by celiac disease. Also, ulcerative colitis and celiac disease can be caused by the same genes. It would be worth looking into. It doesn't sound like he is ruling out celiac disease, but it sure is hard to sit back and wait for more testing. Basically, in order for your daughter to have positive antibodies (EMA and TTG is what they want to see before diagnosis) then her intestines have to be damaged enough for the antibodies being produced to "leak" out into the bloodstream. Know this is what is happening kept me from waiting. I got my children tested through Enterolab and then put them on the diet. This is good for their health (they are all three improving), but they do not have an official diagnosis, which is sometimes hard. You have to consider what is best for you and yours. I would try for the gene test first, and then maybe it won't be necessary to wait for more blood tests.

God bless,

Mariann

Guest gillian502

I'm curious what you mean by "mucosy" stools, because I too have both celiac disease and Colitis, and lately I've noticed my stools are more "fatty" I guess I would say, than usual. I noticed this more since trying the new medication, Asacol, for the colitis. I also have paleness and dark under-eye circles that have not lessened at all since being gluten-free for 9 months. Now I'm wondering if it was the colitis causing this after all. What type of symptoms is your daughter suffering from, and what have they suggested medication-wise? I'm still learning and getting adjusted to the Colitis part of my diagnosis and am eager to talk to others who have people in their lives with both celiac disease and Colitis. It's so hard to tell which one is causing me the problems I'm still having! I'm also wondering if it's possible that my celiac disease diagnosis was incorrect and the disease I've had all along was Colitis, but maybe not since my small intestine did improve on this diet.

stomica Rookie

My daughter's only symptoms are mushy, mucousy stools, usually 2 x day. Rarely, she'll complain of tummy pain right before she poops. She's taking azulfidine, which she's been on for two months. I have no idea what's causing them...I still question the UC diagnosis. Who knows! I hope you're doing well. Keep in touch!

mat4mel Apprentice

Hello :)

I know we have PM'd, but just wanted to tell say my 2 yr old's symptoms sound exactly like yours. She had lots of mucus in her stools, and also complained about her tummy hurting before a bowel movement sometimes. She is also very pale and has dark circles under her eyes. She is a blond hair blue eyed gal anyway, so it might be more noticable with her fair complexion. She has not been really formally diagnosed (I won't do the biopsy) but her two anti-gliadin antibodies were high like your dd's. She didn't have the other antibody tests done. Her stools are so much more normal since going gluten free/casein free. Also wanted to mention that my friend who is a pathologist looked up the #'s for me, and with both tests being positive, there is a 97% chance of my dd having celiac disease. (what the other 3% is, I can't seem to find the answers for). That was enough for me to go gluten free. Anyway, I know I've told you my story a million times. Hang in there, and PM me if you want.

Mel

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

      Fruits & Veggies

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

      heaps of hope!

    3. - knitty kitty replied to mamaof7's topic in Parents, Friends and Loved Ones of Celiacs
      6

      Help understand results

    4. - knitty kitty replied to hjayne19's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      10

      Insomnia help

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

    • Total Members
      132,994
    • Most Online (within 30 mins)
      7,748

    KimberlyS
    Newest Member
    KimberlyS
    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

    • 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!  
    • knitty kitty
      @hjayne19, So glad you found the information helpful.  I know how difficult my struggle with anxiety has been.  I've been finding things that helped me and sharing that with others makes my journey worthwhile. I like Life Extension Bioactive Complete B Complex.  It contains the easily activated forms of B vitamins needed by people with the MTHFR genetic variation often found with Celiac disease.   Avoid B Complex vitamins if they contain Thiamine Mononitrate if possible.  (Read the ingredients listing.)  Thiamine Mononitrate is the "shelf-stable" form of B 1 that the body can't utilize.  B vitamins breakdown when exposed to heat and light, and over time.  So "shelf-stable" forms won't breakdown sitting on a shelf in a bright store waiting to be bought.  (It's also very cheap.)  Thiamine Mononitrate is so shelf-stable that the body only absorbs about thirty percent of it, and less than that is utilized.  It takes thiamine already in the body to turn Thiamine Mononitrate into an active form.   I take MegaBenfotiamine by Life Extension.  Benfotiamine has been shown to promote intestinal healing, neuropathy, brain function, glycemic control, and athletic performance.   I take TTFD-B1 Max by Maxlife Naturals, Ecological Formulas Allthiamine (TTFD), or Thiamax by EO Nutrition.  Thiamine Tetrahydrofurfuryl Disulfide (TTFD for short) gets into the brain and makes a huge difference with the anxiety and getting the brain off the hamster wheel.  Especially when taken with Magnesium Threonate.   Any form of Thiamine needs Magnesium to make life sustaining enzymes and energy.  I like NeuroMag by Life Extension.  It contains Magnesium Threonate, a form of magnesium that easily crosses the blood brain barrier.  My brain felt like it gave a huge sigh of relief and relaxed when I started taking this and still makes a difference daily.   Other brands of supplements i like are Now Foods, Amazing Formulas, Doctor's Best, Nature's Way, Best Naturals, Thorne, EO Nutrition. Naturewise.  But I do read the ingredients labels all the time just to be sure they are gluten and dairy free. Glad to help with further questions.  
    • trents
      Welcome to the celiac.com community @pothosqueen!   Can you be more specific about which IGA test was run that resulted in 114 score and said to be "normal" and could you please include the reference range for what would be normal? By the size of that number it looks like it may have been what we call "total IGA" but that test is not usually run without also running a TTG-IGA. Total IGA tests for IGA deficiency. If someone is IGA deficient, then the celiac-specific IGA tests like the TTG-IGA will be inaccurate. Was this the only IGA test that was run? To answer, your question, yes, a positive biopsy is normally definitive for celiac disease but there are some other medical conditions, some medications and even some food proteins in rare cases that can cause positive biopsies. But it is pretty unlikely that it is due to anything other than celiac disease.
×
×
  • 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.