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

Colitis Or Cc With Gluten


bincongo

Recommended Posts

bincongo Contributor

I posted some comments in the post diagnosis section a few days ago. I was having abdominal pain, leaky gut and constipation. I had had it for 6 days. Well it quit for no apparent reason but in thinking back it seems I go through about 2 weeks of feeling fairly well and then 5 or 6 days of pain. I am a new Celiac of 2 months now so I don't expect to be healed yet but now I think maybe it is a colon issue and not gluten exposure. I have several questions. Are they sometimes related and part of the healing process? Also I think this problem has gotten worse since going gluten free but I do not have diarrhea with it. I have never had diarrhea unless I was having an "IBS" attack prior to my diagnosis. Is constipation ever related to colitis or is it always diarrhea. I have waves of pain and only feel better if I have a stool or pass gas no matter how small. I need help on getting rid of the constipation also. I tryed Mirlax but I actually think it made my pain worse.


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



Celiac.com Sponsor (A8-M):



burdee Enthusiast

I posted some comments in the post diagnosis section a few days ago. I was having abdominal pain, leaky gut and constipation. I had had it for 6 days. Well it quit for no apparent reason but in thinking back it seems I go through about 2 weeks of feeling fairly well and then 5 or 6 days of pain. I am a new Celiac of 2 months now so I don't expect to be healed yet but now I think maybe it is a colon issue and not gluten exposure. I have several questions. Are they sometimes related and part of the healing process? Also I think this problem has gotten worse since going gluten free but I do not have diarrhea with it. I have never had diarrhea unless I was having an "IBS" attack prior to my diagnosis. Is constipation ever related to colitis or is it always diarrhea. I have waves of pain and only feel better if I have a stool or pass gas no matter how small. I need help on getting rid of the constipation also. I tryed Mirlax but I actually think it made my pain worse.

If 'colitis' means abdominal pain without diarrhea, I had lots of 'colitis' over the years. The only time I had cramping pain and diarrhea was when I had c-diff treatment. The antibiotic caused diarrhea, but I still had the pseudomembraneous colitis characteristic of c-diff. I have also had constipation more recently WITHOUT any pain. So I suspect my previous (years of) cramping pain was due to inflammation from gluten and other allergy reactions and/or from gastrointestinal 'bugs' (parasites, pathogenic bacteria and candida). After I finally eliminated my last parasite, took lots of high dose probiotics and HCl supplements for hypochloridia (which caused digestive problems), I no longer had that cramping pain, which was only relieved by passing gas or bowel movements. Now, I rarely have any gas or bloating, but recently became constipated without any of my usual bloating/cramping symptoms. Eating more fiber, drinking more fluids and taking more vitamin C (for the cold I suffered) resolved my constipation

cassP Contributor

I posted some comments in the post diagnosis section a few days ago. I was having abdominal pain, leaky gut and constipation. I had had it for 6 days. Well it quit for no apparent reason but in thinking back it seems I go through about 2 weeks of feeling fairly well and then 5 or 6 days of pain. I am a new Celiac of 2 months now so I don't expect to be healed yet but now I think maybe it is a colon issue and not gluten exposure. I have several questions. Are they sometimes related and part of the healing process? Also I think this problem has gotten worse since going gluten free but I do not have diarrhea with it. I have never had diarrhea unless I was having an "IBS" attack prior to my diagnosis. Is constipation ever related to colitis or is it always diarrhea. I have waves of pain and only feel better if I have a stool or pass gas no matter how small. I need help on getting rid of the constipation also. I tryed Mirlax but I actually think it made my pain worse.

well they DO have that term: Ibs with Constipation.

yes, its possible your body is just going thru phases of healing- but i would suggest you keep checking with your GI and getting a colonoscopy too- just to rule out anything else like Diverticulitis, polyps, an infection... etc.... it is a huge relief im telling you to get one, and rule everything out. i KNEW Celiac was a possibility for me, but i was also worried about Diverticulitis, and the big "C" word. the Gi removed 1 Benign polyp, and gave me a clean bill of health. felt good.

its good to check everything over

bincongo Contributor

well they DO have that term: Ibs with Constipation.

yes, its possible your body is just going thru phases of healing- but i would suggest you keep checking with your GI and getting a colonoscopy too- just to rule out anything else like Diverticulitis, polyps, an infection... etc.... it is a huge relief im telling you to get one, and rule everything out. i KNEW Celiac was a possibility for me, but i was also worried about Diverticulitis, and the big "C" word. the Gi removed 1 Benign polyp, and gave me a clean bill of health. felt good.

its good to check everything over

Thanks for the comments. It is hard to include my whole history but 2 weeks after my endoscopy, that found Celiac, I had a colonoscopy and I do have Diverticulitis but nothing else. It is just that this diet seems to be making my abdominal pain and constipation worse. Now during the times when I don't have pain I feel better than ever. So maybe it is just diverticulitis acting up but I am not sure why it is worse now.

bincongo Contributor

Somewhere on this site people were talking about Magnesium so after my blood work I brought several different suppliments that were recommended. I am beginning to think that the Calcium Magnesium Citrate is my answer to my constipation and pain. I would guess that is somewhat along the line of MOM but different, anyway it is working. Mirlax was making me worse as far as abdominal pain but this Magnesium doesn't. That is my update if anyone has had the same experience.

Archived

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

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

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

    NYC Sidewalk Repair
    Newest Member
    NYC Sidewalk Repair
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • olivia11
      Thanks I am mostly looking for everyday staples and easy meal ideas nothing too specialty if possible.
    • knitty kitty
      There are other Celiac genes. HLA DQ 2 and HLA DQ 8 show up in people from Northern European descent.   People of Mediterranean descent have HLA DQ 7.  People of Asian descent have HLA DQ 9.   There's other Indigenous populations that have other HLA genes that code for Celiac disease.   Are you still having symptoms?   What do you include in your diet?  Are you vegetarian? Are you taking any prescription medication?  Omeprazole?  Metformin?   Do you have anemia?  Thyroid problems? Are you taking any vitamins or herbal supplements?  
    • knitty kitty
      There are eight essential B vitamins.  They are all water soluble.  Any excess of B vitamins is easily excreted by the kidneys.   Thiamine is Vitamin B 1.  Thiamine is safe and nontoxic even in high doses.  Benfotiamine and TTFD are forms of Thiamine that the body can utilize very easily.   The form of Thiamine in the supplements you mentioned is Thiamine Mononitrate, a form that the body does not absorb well and does not utilize well.  Only about thirty percent of the amount on the label is actually absorbed in the small intestine.  Less than that can actually be used by the body.  Manufacturers add thiamine mononitrate to their products because it's cheap and shelf-stable.  Thiamine and other B vitamins break down when exposed to light and heat and over time.  Thiamine Mononitrate is a form that does not break down over time sitting on a shelf waiting for someone to buy them.  What makes Thiamine Mononitrate shelf stable makes it difficult for the body to turn into a useable form.  In fact, it takes more thiamine to turn it into a useable form.   Gastrointestinal Beriberi is a localized shortage of Thiamine in the gastrointestinal tract.  High carbohydrate meals can result in gastrointestinal symptoms of Gastric Beriberi.  Fiber is a type of carbohydrate.  So, high fiber/carbohydrate snacks could trigger Gastric Beriberi.   Since blood tests for Thiamine and other B vitamins are so inaccurate, the World Health Organization recommends trying Thiamine and looking for health improvement because it's safe and nontoxic.  
    • xxnonamexx
      Thanks very interesting I have to see if I should take these 2 vitamins along with my multi and super Vit B complex or if its too much or would hurt me. I don't have any other health issues but would love to see if this improves anything especially to feel stronger build muscle.
    • Roses8721
×
×
  • 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.