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

Collagenous Colitis


raemckee

Recommended Posts

raemckee Newbie

I was just diagnosed with Collagenous colitis but not celiac. I had an endoscopy and colonoscopy a week ago with 6 biopsies along duodendum and colon. I'll be treated with a steroid for the inflammation and advised to follow low fiber, low fat, dairy free, gluten free, no caffeine, no alcohol, cooked fruits and vegetables diet. Do you know of a on-line support group for this? Any recommended reference books? Coping mechanisms?


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



Celiac.com Sponsor (A8-M):



jcronan Rookie

I was just diagnosed with Collagenous colitis but not celiac. I had an endoscopy and colonoscopy a week ago with 6 biopsies along duodendum and colon. I'll be treated with a steroid for the inflammation and advised to follow low fiber, low fat, dairy free, gluten free, no caffeine, no alcohol, cooked fruits and vegetables diet. Do you know of a on-line support group for this? Any recommended reference books? Coping mechanisms?

When I was first tested my doctor said she could definitely see signs of ( and possibly Chrons) but wasn't sure about Celiacs. she followed with a genetic blood test which confirmed it was Celiacs. I would recommend you ask for that if they haven't done it yet. When I asked her what she recommended for treating the first two, she said there was some drugs, but for most patients the change in diet (primarily what you described) is often the best treatment. It can take a little longer than if you are just dealing with one thing, but hopefully you will get results. I've been Gluten Free for 2 1/2 months now & have started to see improvement in all areas.

raemckee Newbie

The steroid prescribed is Budesonide EC 3 mg. The warnings said let your Dr. know if you have glaucoma. I have recently been diagnosed with that as well. Has anyone else had experience with the same scenario? I have contacted both the gastroenterologist and the opthamologist and am waiting for them to respond back. If you have collagenous colitis and have taken steroid treatment, please let me know about your experience as well.

GFinDC Veteran

You might get some info on the Crohn's forum. They have a pretty active forum there.

For gluten free eating info though the best place is right here on celiac com.

Open Original Shared Link

peeptoad Apprentice

My dad has collagenous colitis. He was on Entocort for awhile, but now mainly just a modified diet and that seems to keep him in remission. The main things he avoids are beans/legumes, large amounts of raw vegetables (particularly leafy greens, bell peppers, etc) and a few other things.

You might try the FODMAP diet, or some modified version of ti to see if it works for you.

The other thing that his GI doctor told him was that Pepto Bismol is great for CC. There is something in it that has a positive effect on the microflora or something. My dad has found it to be a big help.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,869
    • Most Online (within 30 mins)
      7,748

    Stacy W
    Newest Member
    Stacy W
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      I totally get this. It's absolutely a grieving process, and it's okay to feel gutted about the loss of those simple joys, especially at 18. Your feelings are completely valid—it's not about being ungrateful for your amazing boyfriend, it's about mourning the life you thought you'd have. That "tortured by the smell" feeling is so real. It does get easier, I promise, but it's okay to sit in the sadness and just vent about how much it stings right now. Thanks for sharing that. Celiac.com has published a book on our site by Jean Duane PhD called Gluten-Centric Culture, which covers many of the social aspects of having celiac disease: This chapter in particular covers issues around eating with family and others - Gluten-Centric Culture: Chapter 5 - Grabbing A Bite Together:    
    • Scott Adams
      Many of us with celiac find that the fillers in medications can cause a reaction, and sometimes our bodies just process things weirdly. That "rebound muscle pain" and "burning feet" you described sounds awful and is a huge red flag. It's frustrating enough managing the diet without medication causing setbacks. So sorry you're dealing with this, but you're definitely on the right track by connecting the dots. You can search this site for prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
    • Scott Adams
      It's so tough when you're doing everything right and still get hit with it. I'm glad you're figuring out a system that works for you—the peppermint tea and rehydration powders are smart moves. It sounds like you've really learned to listen to your body, and that's half the battle. Sticking to simple, safe food at home is the best way to build yourself back up. It's great you can take the time to rest properly. Thanks for sharing what works; it's a big help to others figuring this out too. This article, and the comments below it, may be helpful:    
    • Scott Adams
      I am so sorry you're going through this. It's bad enough to fight for a diagnosis and manage this disease, but to have your partner use it as a weapon against you is truly devastating. What you're describing isn't just a lack of support; it's abuse, full stop. Controlling your food and money is cruel, and his pleasure in your misery is chilling. Please hear this: the kindness from that woman at the food pantry is what you deserve. It's a glimpse of the real world, where people care. You deserve to eat, to heal, and to have peace. His actions are the biggest barrier to your health right now, and you are not broken—you are surviving in an impossible situation. Don't give up on that lifeline you've found.
    • Colleen H
      Thank you.. Christina My anxiety is through the roof.  I think it was from eggs.  I really don't know because my eyes feel sore. Like I'm allergic to them.  I was defient in B12.   My heart is pounding and it won't stop.  Not sure what to do.   I don't have much support other than this forum.    Colleen 
×
×
  • 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.