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. - cristiana replied to Dizzyma's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      2

      Newly diagnosed mam to coeliac 11 year old

    2. - trents replied to Dizzyma's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      2

      Newly diagnosed mam to coeliac 11 year old

    3. - Dizzyma posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      2

      Newly diagnosed mam to coeliac 11 year old

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

    • Total Members
      132,923
    • Most Online (within 30 mins)
      7,748

    cmckurtz
    Newest Member
    cmckurtz
    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

    • cristiana
      Hi @Dizzyma I note what @trents has commented about you possibly posting from the UK.  Just to let you know that am a coeliac based in the UK, so if that is the case, do let me know if can help you with any questions on the NHS provision for coeliacs.    If you are indeed based in the UK, and coeliac disease is confirmed, I would thoroughly recommend you join Coeliac UK, as they provide a printed food and drink guide and also a phone app which you can take shopping with you so you can find out if a product is gluten free or not. But one thing I would like to say to you, no matter where you live, is you mention that your daughter is anxious.  I was always a bit of a nervous, anxious child but before my diagnosis in mid-life my anxiety levels were through the roof.   My anxiety got steadily better when I followed the gluten-free diet and vitamin and mineral deficiencies were addressed.  Anxiety is very common at diagnosis, you may well find that her anxiety will improve once your daughter follows a strict gluten-free diet. Cristiana 
    • trents
      Welcome to the celic.com community @Dizzyma! I'm assuming you are in the U.K. since you speak of your daughter's celiac disease blood tests as "her bloods".  Has her physician officially diagnosed her has having celiac disease on the results of her blood tests alone? Normally, if the ttg-iga blood test results are positive, a follow-up endoscopy with biopsy of the small bowel lining to check for damage would be ordered to confirm the results of "the bloods". However if the ttg-iga test score is 10x normal or greater, some physicians, particularly in the U.K., will dispense with the endoscopy/biopsy. If there is to be an endoscopy/biopsy, your daughter should not yet begin the gluten free diet as doing so would allow healing of the small bowel lining to commence which may result in a biopsy finding having results that conflict with the blood work. Do you know if an endoscopy/biopsy is planned? Celiac disease can have onset at any stage of life, from infancy to old age. It has a genetic base but the genes remain dormant until and unless triggered by some stress event. The stress event can be many things but it is often a viral infection. About 40% of the general population have the genetic potential to develop celiac disease but only about 1% actually develop celiac disease. So, for most, the genes remain dormant.  Celiac disease is by nature an autoimmune disorder. That is to say, gluten ingestion triggers an immune response that causes the body to attack its own tissues. In this case, the attack happens in he lining of the small bowel, at least classically, though we now know there are other body systems that can sometimes be affected. So, for a person with celiac disease, when they ingest gluten, the body sends attacking cells to battle the gluten which causes inflammation as the gluten is being absorbed into the cells that make up the lining of the small bowel. This causes damage to the cells and over time, wears them down. This lining is composed of billions of tiny finger-like projections and which creates a tremendous surface area for absorbing nutrients from the food we eat. This area of the intestinal track is where all of our nutrition is absorbed. As these finger-like projections get worn down by the constant inflammation from continued gluten consumption before diagnosis (or after diagnosis in the case of those who are noncompliant) the efficiency of nutrient absorption from what we eat can be drastically reduced. This is why iron deficiency anemia and other nutrient deficiency related medical problems are so common in the celiac population. So, to answer your question about the wisdom of allowing your daughter to consume gluten on a limited basis to retain some tolerance to it, that would not be a sound approach because it would prevent healing of the lining of her small bowel. It would keep the fires of inflammation smoldering. The only wise course is strict adherence to a gluten free diet, once all tests to confirm celiac disease are complete.
    • Dizzyma
      Hi all, I have so many questions and feel like google is giving me very different information. Hoping I may get some more definite answers here. ok, my daughter has been diagnosed as a coeliac as her bloods show anti TTG antibodies are over 128. We have started her  on a full gluten free diet. my concerns are that she wasn’t actually physically sick on her regular diet, she had tummy issues and skin sores. My fear is that she will build up a complete intolerance to gluten and become physically sick if she has gluten. Is there anything to be said for keeping a small bit of gluten in the diet to stop her from developing a total intolerance?  also, she would be an anxious type of person, is it possible that stress is the reason she has become coeliac? I read that diagnosis later in childhood could be following a sickness or stress. How can she have been fine for the first 10 years and then become coeliac? sorry, I’m just very confused and really want to do right by her. I know a coeliac and she has a terrible time after she gets gluttened so just want to make sure going down a total gluten free road is the right choice. thank you for any help or advise xx 
    • xxnonamexx
      very interesting thanks for the info  
    • Florence Lillian
      More cookie recipes ...thanks so much for the heads-up Scott.  One can never have too many.  Cheers, Florence.
×
×
  • 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.