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

More Constipated On gluten-free Diet


ElenaDragon

Recommended Posts

ElenaDragon Explorer

I started the gluten-free diet nearly a week ago, and my gas has definitely been reduced. However, I'm still have abdominal pain, and I think it's because I'm still constipated, even more so than before I started the gluten-free diet. I'm getting the same amount of fiber per day (about 35g on average), but my daily morning stool is not loose like it used to be, so I don't go as much. The stool is probably much more normal now (formed instead of loose), but I feel like my whole system is backed up and giving me pain. The pain is mostly on the left side, but some on the right as well - I was having this pain before I started the gluten-free diet.

I've also been taking Miralax for a few weeks now at 1/2 dose per day. Last night I upped it to a whole dose, and I'm going to try that for a while to see if it helps.

Is the fiber from a non gluten diet different in some way from gluten fiber? Or could it be that my system normally moves slowly and the gluten was making it move more quickly?


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



Celiac.com Sponsor (A8-M):



Teacher1958 Apprentice

Hi,

I've been on the diet for almost four months. It does take awhile for your digestive tract to get accustomed to the changes. I noticed a little bit of what you're talking about at first. I would go a day or day-and-a-half without a BM, which I considered constipation, but for manypeople probably isn't constipation. (We're just used to going a lot.) I didn't take anything for it, though. I wanted to let my body normalize on its own.

The gas reduction for me was amazing! I was so glad to not have to think about it all the time, worrying that I would embarrass myself by passing gas in public. The only positive thing about gas is that it does help move things along, so I think that could be another reason you're not going as often.

I'm sure there are "veterans" on here who can speak to this better than I, but that's my take on it.

Guest j_mommy

I had the same problem when I first started the diet and it took me about a month and a half not to be "constipated". But as teacher said...our constipation is not real constipation. Not going EVERY day is ok...not ideal but ok. Your body will work it self out after it's had time to heal. If you're still "constipated" in a month or so then worry!!! Your belly could not be feeling right b/c it's only been a short time. Some people take months to feel a change, some it's weeks and some notice right away. Everyone is diffrent.

Long story short...give your body time to heal!!!!

ElenaDragon Explorer

Thank you both for your responses. Teacher, I think you're right that the gas was probably helping to move things along. But for me flatulence wasn't the problem, it was getting the gas to come out! The gas would stay trapped inside me for many hours, very uncomfortable and very noisy, and would prevent me from passing stool. Once the gas finally came out (usually while I was sleeping), I would have D in the morning. I guess I just got used to this routine since it did work to clear me out, but it often made my evenings very uncomfortable.

I wouldn't be that worried if I wasn't having all the abdominal pain. My GI thought my intestines are spasming and gave me Bentyl, which does not help (so I stopped taking it). I will give it some more time though, and give the diet a chance to work and my body a chance to adjust!

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. - Jmartes71 replied to Jmartes71's topic in Related Issues & Disorders
      13

      My only proof

    2. - marion wheaton posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Are Lindt chocolate balls gluten free?

    3. - Dorothy O. commented on Scott Adams's article in Latest Research
      7

      Study Estimates the Costs of Delayed Celiac Disease Diagnosis (+Video)

    4. - JoJo0611 replied to JoJo0611's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      4

      CT with contrast.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,400
    • Most Online (within 30 mins)
      7,748

    ed m
    Newest Member
    ed m
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Jmartes71
      I have been diagnosed with celiac in 1994, in remission not eating wheat and other foods not to consume  my household eats wheat.I have diagnosed sibo, hernia ibs, high blood pressure, menopause, chronic fatigue just to name a few oh yes and Barrett's esophagus which i forgot, I currently have bumps in back of my throat, one Dr stated we all have bumps in the back of our throat.Im in pain.Standford specialist really dismissed me and now im really in limbo and trying to get properly cared for.I found a new gi and new pcp but its still a mess and medical is making it look like im a disability chaser when Im actively not well I look and feel horrible and its adding anxiety and depression more so.Im angery my condition is affecting me and its being down played 
    • marion wheaton
      Wondering if anyone knows whether Lindt chocolate balls are gluten free. The Lindt Canadian website says yes but the Lindt USA website says no. The information is a bit confusing.
    • JoJo0611
      I didn’t know there were different types of CT. I’m not sure which I had. It just said CT scan with contrast. 
    • Scott Adams
    • Scott Adams
      I had the same thing happen to me at around your age, and to this day it's the most painful experience I've ever had. For me it was the right side of my head, above my ear, running from my nerves in my neck. For years before my outbreak I felt a tingling sensation shooting along the exact nerves that ended up exactly where the shingles blisters appeared. I highly recommend the two shot shingles vaccine as soon as your turn 50--I did this because I started to get the same tingling sensations in the same area, and after the vaccines I've never felt that again.  As you likely know, shingles is caused by chicken pox, which was once though of as one of those harmless childhood viruses that everyone should catch in the wild--little did they know that it can stay in your nervous system for your entire life, and cause major issues as you age.
×
×
  • 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.