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

Mucos In Stool


danikali

Recommended Posts

danikali Enthusiast

I have been noticing mucos in my stool again :blink: (I know, gross) ...... and I don't remember....... is this a sign of malnutrition or could this be nothing at all? :huh:


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



Celiac.com Sponsor (A8-M):



nettiebeads Apprentice
I have been noticing mucos in my stool again  :blink: (I know, gross) ...... and I don't remember....... is this a sign of malnutrition or could this be nothing at all?  :huh:

<{POST_SNAPBACK}>

Are you gluten-free right now? Have you had gluten? How long have you had celiac disease? I think it's your body's way of protecting itself from what it considers harmful, rightly or wrongly. Mucus in stools is one of the symptoms of celiac disease.

danikali Enthusiast

Hi,

I have been 100% gluten free starting only Monday actually. I'm actually still in the process of being diagnosed. I just got blood tests done and sent in samples to enterolab; I'm waiting on results from everything, still.

Anyway, I know I have a problem with gluten though because I have tried the gluten free diet before, and felt a lot better, but kept getting "glutened" when I would eat any processed foods or from resturants because I was naive on all of the hidden products that use it. Anyway, I went back on gluten to get the tests done and was sick as a dog everyday, and now I am almost feeling like myself again. Some of the symptoms have been subsiding, and I have A LOT more energy and my arms and muscles don't feel so weak. But for the past couple of days, I've noticed mucos in my stool again and I was just wondering......... <_<

I guess my question is: mucos in your stool isn't normal, right? Because I know when I was diagnosed with "IBS" and did A LOT of research on it, I learned that mucos in the stool was a sign of IBS (I don't believe in IBS now)........but I'm kinda wondering all of this because if muscos in the stool goes along with the doctor favorite, "IBS," and "IBS" suposedly does not "harm" your body, then that means mucos in the stool doesn't mean that your body is being "harmed?"

I don't know......I hope I didn't confuse you! :blink:

Thanks for any help though! :rolleyes:

  • 1 month later...
Candy Contributor

Hi Ya,

I noticed mucus in my stools too, just recently, and I had already suspected Celiac for quite a few months.When I saw the mucus I thought God,I'm dying.It wasn't a whole lot of mucus,but it was noticable.I haven't seen it since and have been eating gluten free products only recently,but I feel no discomfort,see no more mucus,so I guess it was the Gluten.I avoid it with more determination now.

Hi Ya,

I noticed mucus in my stools too, just recently, and I had already suspected Celiac for quite a few months.When I saw the mucus I thought God,I'm dying.It wasn't a whole lot of mucus,but it was noticable.I haven't seen it since and have been eating gluten free products only recently,but I feel no discomfort,see no more mucus,so I guess it was the Gluten.I avoid it with more determination now.

StrongerToday Enthusiast

I noticed mine seem a bit off if I've had something greasy - chips, bacon, etc. Have you tried keeping a food log?

jerseyangel Proficient

I had the mucus also pre DX. It continued even after I cut out gluten, but after the first couple of months, dissapeared. I never have a problem with it now, even if glutened.

jenvan Collaborator

Your body produces some mucous normally to help lube up the intestines...however, increased mucous can be a sign of intestinal irritation--which goes along with Celiac. A little more info on it here: Open Original Shared Link


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



Celiac.com Sponsor (A8-M):



Nancym Enthusiast

I get this too. It concerns me because I know the intestinal wall consists of a mucosal wall that is one cell thick and is supposed to keep the intestinal contents out of the blood stream. So when I see mucos in my stool, I'm always afraid it's this precious wall!

ownedbykira Newbie

May I ask ...what does mucus in the stool look like, it is not like white gooey stuff attached to the stool

jerseyangel Proficient

Pretty much...

Rachel--24 Collaborator

I had alot of mucus pre-gluten-free....I never see it anymore though.

May I ask ...what does mucus in the stool look like, it is not like white gooey stuff attached to the stool

The mucus I was seeing looked like ummm....well... it looked like mucus. :huh:

Sorry, yes, it was gooey stuff mixed in the stool...it looked kind of clear I guess. Well, it looked like it would have been clear had it not been in the stool. Sometimes it would be very visible like a long strand of mucus.

Sorry to be so graphic but I was just answering the question. :P

Pretty much...

:lol::lol:

Good answer Patti. :)

jerseyangel Proficient

I figured it was easier that way :D

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,563
    • Most Online (within 30 mins)
      7,748

    Bob Madden
    Newest Member
    Bob Madden
    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

    • Flash1970
      Thank you for the links to the articles.  Interesting reading. I'll be telling my brother in law because he has a lot of pain
    • Scott Adams
      Oats naturally contain a protein called avenin, which is similar to the gluten proteins found in wheat, barley, and rye. While avenin is generally considered safe for most people with celiac disease, some individuals, around 5-10% of celiacs, may also have sensitivity to avenin, leading to symptoms similar to gluten exposure. You may fall into this category, and eliminating them is the best way to figure this out. Some people substitute gluten-free quinoa flakes for oats if they want a hot cereal substitute. If you are interested in summaries of scientific publications on the topic of oats and celiac disease, we have an entire category dedicated to it which is here: https://www.celiac.com/celiac-disease/oats-and-celiac-disease-are-they-gluten-free/   
    • knitty kitty
    • knitty kitty
      Hi, @Ginger38, I've had shingles in the past.  I understand how miserable you're feeling.   Not only do i have the chickenpox virus lurking about, I also have the cold sore virus that occasionally flares with a huge cold sore on my lip when stressed or exposed to gluten.  The virus lives dormant in the nerves on the left side of my face.  It causes Bell's Palsy (resulting in drooling).  The cold sore virus is also in my eye.  My eye swells up and my vision is diminished permanently whenever I have a flare, so it's of the utmost importance to keep flares away and treat them immediately if they do happen so I don't lose any more vision.   I take the amino acid supplement L-Lysine.  Lysine messes with the replication of viruses, which helps the body fight them off.   I haven't had an outbreak for several years until this year when exceptionally stressed and contaminated, it flared up again. Lysine has been shown to be beneficial in suppression of viruses like the cold sore virus (a herpetic virus), the chickenpox virus (also a herpetic virus), as well as the HIV virus, and even the Covid virus.   I also take additional Thiamine in the form TTFD (tetrahydrofurfuryl disulfide) because Thiamine has antiviral properties as well.   For pain, a combination of Thiamine (like TTFD or Benfotiamine or Thiamine Hydrochloride), with B12 Cobalamine, and Pyridoxine B6 have been shown to have analgesic properties which relieve pain and neuropathy.    The combination of Thiamine B1, Pyridoxine B6 and Cobalamine B12 really does work to relieve pain.  I take it for back pain from crushed vertebrae in my back.  This combination also works on other pain and neuropathy.   I usually buy a supplement that combines all three and also Riboflavin B2 called EXPLUS online.  However, it's made in Japan and the price with the tariffs added makes it really expensive now.  But the combination of Thiamine B1, Pyridoxine B6 and B12 Cobalamine (and Riboflavin B2) still work even if taken separately.   I can't take Tylenol or ibuprofen because of stomach upsets.  But I can take the vitamin combination without side effects.  However, you can take the three vitamins at the same time as other pain relievers for added benefit.  The vitamins help other pain relievers work better. I hope you will try it.  Hopeful you'll feel better quickly. Interesting Reading: Thiamine, cobalamin, locally injected alone or combination for herpetic itching: a single-center randomized controlled trial https://pubmed.ncbi.nlm.nih.gov/23887347/ Mechanisms of action of vitamin B1 (thiamine), B6 (pyridoxine), and B12 (cobalamin) in pain: a narrative review https://pubmed.ncbi.nlm.nih.gov/35156556/ Analgesic and analgesia-potentiating action of B vitamins https://pubmed.ncbi.nlm.nih.gov/12799982/ A Narrative Review of Alternative Symptomatic Treatments for Herpes Simplex Virus https://pmc.ncbi.nlm.nih.gov/articles/PMC10301284/
    • Mari
      I think, after reading this, that you areso traumatized by not being able yo understand what your medical advisors have been  what medical conditions are that you would like to find a group of people who also feel traumatized who would agree with you and also support you. You are on a crusade much as the way the US Cabinet  official, the Health Director of our nation is in trying to change what he considers outdated and incorrect health advisories. He does not have the education, background or experience to be in the position he occupies and is not making beneficial decisions. That man suffered a terrible trauma early in his life when his father was assonated. We see now how he developed and worked himself into a powerful position.  Unless you are willing to take some advice or  are willing to use a few of the known methods of starting on a path to better health then not many of us on this Celiac Forum will be able to join you in a continuing series of complaints about medical advisors.    I am almost 90 years old. I am strictly gluten free. I use 2 herbs to help me stay as clear minded as possible. You are not wrong in complaining about medical practitioners. You might be more effective with a clearer mind, less anger and a more comfortable life if you would just try some of the suggestions offered by our fellow celiac volunteers.  
×
×
  • 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.