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

Ridiculously Bloated, "stopped Up", Etc


DownWithGluten

Recommended Posts

DownWithGluten Explorer

Hmm. Something tells me this has probably come up before, but I don't come on here too much. Feel free to direct me or, tell me to be quiet, if it has! lol.

Anyway. Just a recap. I was not diagnosed with Celiac's or anything. I was diagnosed with IBS. But nothing worked much. (was given a medication that just made me bleed...how nice!) So in desperation I prepared myself to go gluten-free in hopes for my life to change...in a good way. (Besides the obvious food changes ;) ). And, I have earlier this month.

So, I've been gluten-less (at least, that I am aware of!) since January 8th. Not too long. And I have to say, I got extremely bloated/constipated within the past 2 weeks. Absurdly. Worse than Ive had before. It feels like I have a cement block lodged between my pelvis and chest. I don't even want to eat, because I know I'm just 'adding' to the 'pile' that is already going up my chest. Half expect an alien to burst out of my midsection. I'm used to abdominal pain of various sorts, but haven't had it quite in this manner before. I was IBS C-D...meaning, my problem was being constipated kinda for a while, then having the 'd' come in an extremely painful ordeal to expel it all out. Not fun at all. Also, I got gas bloating a lot. But...now...the constipation is different than I've ever felt before! Much thicker feeling, tight, distended, and just generally painful.

So, I'm not sure what's going on. Is just this part of the ever-fun process of going gluten-free, or what? lol. Could the rice pasta be somehow slowing things down? I really don't know, and am curious if others have this problem too. It's not horrendous pain or anything, just extremely uncomfortable but, more important - not like I've felt before! The first week...I was amazed because Iw as actually 'going' every day, which usually never happens. It got my hopes up! Then it just stopped dead and now is all weird.

All right, you get the point. Any input anyone might have to offer? Thanks!


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



Celiac.com Sponsor (A8-M):



Ursa Major Collaborator

If you are eating white rice pasta, that could definitely make you constipated. You may want to make sure you eat enough fiber, and drink lots of water. Also, try prune juice.

Another thing that could make you constipated is dairy. You might want to eliminate it for at least six months as well.

IBS is not really a diagnosis. It just means that your doctor hasn't got a clue what is wrong, and declare the symptoms to be your diagnosis! If your bowels are irritated, there is a reason. Throwing medication at the symptom is crazy, without looking for the cause.

I hope you'll start feeling better soon.

DownWithGluten Explorer

Thanks for the info. I think the pasta I've had a few times is brown rice but...yeah.

I suppose it could be dairy, too. I ate that beforehand but...I don't know. I'll try to cut down on that a little and see if it makes a difference.

And yes, I agree about the IBS thing. I used to post on a board for that, and maybe 20% had similar symptoms to me. The rest - not even close. So, whatever that 20% had is probably the same as me. But not the other 80%. Yet we're all given the IBS label! I think that not only could some be misdiagnosed cases...but perhaps there are some digestive issues that haven't even been articulated yet that some of us could have. Never know...

And yeah. The medication was meant to regulate. It did for about the first week, but then my digestion just lapsed back to its old routine. Not to mention the bleeding. So I stopped taking it.

Oh, and I've never tried prune juice! Perhaps I should look into that.

kbabe1968 Enthusiast

Aura -

I just went gluten free as well (Jan 1st). I was diagnosed with IBS also but my doc was not in the pill throwing mode, so gave me some lifestyle changes I could do (exercise, fiber, etc). I decided to go gluten free to see if it was celiac.

DEFINITELY make sure you're getting enough fiber. I was a "whole wheat" junkie - the more fiber the better when I was a glutener. I've noticed that I can go for days now without going. SO...eat LOTS of fruit and veggies. Drink veggie juices (fresh if it's possible). ALSO, careful not to eliminate all the fats from your diet too - believe it or not fat aids in "moving" things (GOOD FATS...I'm not talking french fries here!). Nuts can be very fiberous as well. Walnuts & Almonds are good for movement. ALSO, make sure you are drinking water (not just liquids - things like sodas and such can block you as well)

If you eat a lot of rice, rice pasta and potatoes, you are going to block FAST.

IF you need immediate relief do this - Drink 32 ozs of water in a 15 minute period. Wait an hour. If you still haven't gone, do it again. BUT if you don't go after that - DON'T DO IT AGAIN for at least two hours. TOO much water in a short period of time can be bad and cause water intoxication. I used to get C all the time when travelling. My husbands and my first trip together (when we were engaged and I went to meet his dad). I didn't go for six whole days. AT ALL. I finally took an exlax - but hated it! The next time this happened, I followed the water treatment, and it worked better than anything I've ever used.

GOOD LUCK!!!

Corkdarrr Enthusiast

Taking a daily magnesium supplement can also keep you regular. I take two a day, but when I start to feel stopped up I might double it for a day or two until things start going again.

Nancym Enthusiast

I'm pretty sure my constipation was caused by dairy products but when I was eating wheat it gave me diarrhea, so they kind of balanced out... but once I cut out the wheat, the constipation took over full time. :P I've cut out the diary too, and all other grains as well, and things are almost like clockwork. I give a lot of credit to drinking kefir made from coconut milk.

ReneCox Contributor

I sometimes take flax seed oil and that seems to help alot too


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



Celiac.com Sponsor (A8-M):



tarnalberry Community Regular

I would second the magnesium. There's less of it in the refined gluten-free flours. If you're not using the more complex gluten-free grains yet (quinoa, amaranth, buckwheat, etc.) I'd encourage looking into those.

hathor Contributor

I sometimes take flax seed oil and that seems to help alot too

Or you can use ground flax seed, which gives you fiber.

I agree with the suggestion about dairy.

I'm not giving any more advice because I'm still new to avoiding gluten (only 3 weeks at this point -- it looks like a few days longer than you) and my bowels aren't working how they should yet -- or I don't know if they are yet. First I had no change from my usual C, then it got worse, then I had an inexplicable explosion a week ago over the course of an hour (all that came from me :blink: ), a week passes with nothing, and finally this morning I had a normal (for normal people :lol: ) movement. I know, too much information. Nothing like having a safe forum for discussing one's poo :D

Anyway, I offer my experience to show that it isn't just you! I'm keeping a food diary to see if I can find some pattern. But it could be that my body is still adjusting to not having the irritant of the gluten. I can't remember a time when my bowels worked properly. Some other people have mentioned to me that it took their bodies 3 months to settle down to a healthy pattern.

I'll have to compare things to when I have had quinoa and buckwheat. What I've noticed is quite an impact from popcorn.

If things stay strange, I'm considering magnesium supplementation as a last resort.

In the meantime, I'm sending the Enterolab package tomorrow. Then I can find out if this gluten-free thing is just a fanciful notion on my part. Other things have improved, but I don't want to be fooled by a placebo effect.

DownWithGluten Explorer

Thanks for the suggestions so far... *takes mental note of what everyone said*

Could be something to the dairy/cheese thing, I think!

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - AlwaysLearning replied to Colleen H's topic in Coping with Celiac Disease
      3

      Gluten related ??

    2. - Colleen H replied to Colleen H's topic in Coping with Celiac Disease
      3

      Gluten related ??

    3. - Jmartes71 replied to Jmartes71's topic in Coping with Celiac Disease
      4

      My only proof

    4. - AlwaysLearning replied to Jmartes71's topic in Coping with Celiac Disease
      4

      My only proof

    5. - AlwaysLearning replied to Colleen H's topic in Coping with Celiac Disease
      3

      Gluten related ??


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,084
    • Most Online (within 30 mins)
      7,748

    bigwave
    Newest Member
    bigwave
    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

    • AlwaysLearning
      Get tested for vitamin deficiencies.  Though neuropathy can be a symptom of celiac, it can also be caused by deficiencies due to poor digestion caused by celiac and could be easier to treat.
    • Colleen H
      Thank you so much for your response  Yes it seems as though things get very painful as time goes on.  I'm not eating gluten as far as I know.  However, I'm not sure of cross contamination.  My system seems to weaken to hidden spices and other possibilities. ???  if cross contamination is possible...I am in a super sensitive mode of celiac disease.. Neuropathy from head to toes
    • Jmartes71
      EXACTLY! I was asked yesterday on my LAST video call with Standford and I stated exactly yes absolutely this is why I need the name! One, get proper care, two, not get worse.Im falling apart, stressed out, in pain and just opened email from Stanford stating I was rude ect.I want that video reviewed by higher ups and see if that women still has a job or not.Im saying this because I've been medically screwed and asking for help because bills don't pay itself. This could be malpratice siit but im not good at finding lawyers
    • AlwaysLearning
      We feel your pain. It took me 20+ years of regularly going to doctors desperate for answers only to be told there was nothing wrong with me … when I was 20 pounds underweight, suffering from severe nutritional deficiencies, and in a great deal of pain. I had to figure it out for myself. If you're in the U.S., not having an official diagnosis does mean you can't claim a tax deduction for the extra expense of gluten-free foods. But it can also be a good thing. Pre-existing conditions might be a reason why a health insurance company might reject your application or charge you more money. No official diagnosis means you don't have a pre-existing condition. I really hope you don't live in the U.S. and don't have these challenges. Do you need an official diagnosis for a specific reason? Else, I wouldn't worry about it. As long as you're diligent in remaining gluten free, your body should be healing as much as possible so there isn't much else you could do anyway. And there are plenty of us out here who never got that official diagnosis because we couldn't eat enough gluten to get tested. Now that the IL-2 test is available, I suppose I could take it, but I don't feel the need. Someone else not believing me really isn't my problem as long as I can stay in control of my own food.
    • AlwaysLearning
      If you're just starting out in being gluten free, I would expect it to take months before you learned enough about hidden sources of gluten before you stopped making major mistakes. Ice cream? Not safe unless they say it is gluten free. Spaghetti sauce? Not safe unless is says gluten-free. Natural ingredients? Who knows what's in there. You pretty much need to cook with whole ingredients yourself to avoid it completely. Most gluten-free products should be safe, but while you're in the hypersensitive phase right after going gluten free, you may notice that when something like a microwave meal seems to not be gluten-free … then you find out that it is produced in a shared facility where it can become contaminated. My reactions were much-more severe after going gluten free. The analogy that I use is that you had a whole army of soldiers waiting for some gluten to attack, and now that you took away their target, when the stragglers from the gluten army accidentally wander onto the battlefield, you still have your entire army going out and attacking them. Expect it to take two years before all of the training facilities that were producing your soldiers have fallen into disrepair and are no longer producing soldiers. But that is two years after you stop accidentally glutening yourself. Every time you do eat gluten, another training facility can be built and more soldiers will be waiting to attack. Good luck figuring things out.   
×
×
  • 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.