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

Is Ibs Common With Celiac?


JulesH

Recommended Posts

JulesH Rookie

I know that the symptoms for IBS and celiac are very similar and they are often confused, but my doctor is now telling me that he thinks I have both.

I was diagnosed with celiac about a year and a half ago, by colonoscopy which found sprue and then a follow up blood test. So I think there's no question that I have celiac. But I have stomach issues that have cropped up more recently (and are not due to unintentional gluten intake, I've made absolutely sure of that) that my doctor is now saying is probably IBS. He actually said that he's thought that I have had IBS for a while, but when the celiac diagnosis came up, he just attributed everything to that.

So, am I just unlucky and beat the odds and have both, or is this something common?


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



Celiac.com Sponsor (A8-M):



jerseyangel Proficient

Yes, according to my gastroenterologist it's quite possible to have both. I do, and mine is caused by additional food intolerance.

It's not uncommon for a Celiac to go gluten-free, then weeks or months later get symptoms again. The best thing to do is an elimination diet to try and uncover what other foods may be causing your symptoms.

We hear a lot of "IBS is a catchall diagnosis"--and that's true if the doctor is not willing to dig deeper and attempt to find the cause. I think of IBS as more of a symptom than a diagnosis. It's not normal to have chronic D or be constipated most of the time. If you are truly gluten-free, and are sure you aren't getting gluten, I would suggest cutting out dairy, soy and corn (one at a time) and see if that makes any difference.

I also take a Caltrate 600 with vitamin D twice a day--it is quite helpful for IBS with D.

loraleena Contributor

IBS is the number one misdiagnosis for Celiac. It is a garbage can diagnosis for when the doc does not know why you are having stomach issues.

JulesH Rookie

Thank you for the responses. My doctor is not trying to take back the diagnosis of celiac, and he is very conscientious, and is doing further testing to make sure there is nothing else that could be causing my stomach problems. He told me that for my own well being I should look into it, and I'm inclined to trust him and take the medication to make my stomach stop hurting.

Judyin Philly Enthusiast
Thank you for the responses. My doctor is not trying to take back the diagnosis of celiac, and he is very conscientious, and is doing further testing to make sure there is nothing else that could be causing my stomach problems. He told me that for my own well being I should look into it, and I'm inclined to trust him and take the medication to make my stomach stop hurting.

HI

I have both and have been gluten-free and other foods for 2 1/2 years. What medicine did he put you on and was it for the IBS?

Judy

JulesH Rookie
HI

I have both and have been gluten-free and other foods for 2 1/2 years. What medicine did he put you on and was it for the IBS?

Judy

None, yet. I'm having an ultrasound and CT today to confirm that there's nothing else, but if everything else is fine, he said he'd put me on an anti-spasmodic. I can't remember which specifically he mentioned, though.

Nancym Enthusiast

I found that continuing intestinal symptoms were due to other foods I'm sensitive to. When I follow a very basic diet of meat and veggies (and a few other things) my IBS clears up. So I'm always trying to identify what the heck it was I ate that set me off.

The "Big Eight" list of things people are allergic to (food-wise) is probably a good place to start:

Soy

Wheat

Milk -- dairy

Shellfish

Peanuts

Tree nuts

Fish

Eggs

But right now I'm suspecting chocolate, SF chewing gum, a sugar free raspberry syrup I'm using. I've eliminated all of them and I'll reintroduce them slowly and see how Mr. Gut feels. Right now, all is quite on the southern frontier so it is time to test something.


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



Celiac.com Sponsor (A8-M):



Judyin Philly Enthusiast

Jules......how did your tests go today?

Judy

jayhawkmom Enthusiast
But right now I'm suspecting chocolate, SF chewing gum,

Ya know what?? I always chew the same kind of gum, but the store was out of my preferred brand the other day. So, I bought something different. Without reading the ingredients (I know... BAD) I shoved a piece in my mouth and began to chew vigorously.

Within minutes, my entire face was itchy - and my throat felt tight.

I'm fairly certain that I've developed a wheat allergy - and *that* is my typical reaction to cross-contamination and wheat ingestion. So, it would not surprise me, at all, if there is wheat in your gum!!!

I wish I could remember what kind it was that I bought. It was "stick" sugar free gum. I normally buy Orbit gum and have not had any problems with that.

happygirl Collaborator

FYI:

"Q: Are there some celiacs who do not respond to the gluten-free diet?

A few patients have a poor clinical and/or histologic (biopsy) response to the diet. An important step in assessing patients who are non-responders is to confirm the diagnosis of celiac disease by review of the original biopsy, preferably by an expert gastrointestinal pathologist. However, the most common cause of a poor response is continued gluten ingestion, which may be intentional or unintentional.

An intolerance to other foods, such as lactose and fructose or soy can be a reason for lack of improvement. Some non-responders may have reversible pancreatic insufficiency or bacterial overgrowth, requiring treatment. Colonoscopy might indicate other causes of the failure to respond, such as microscopic colitis or inflammatory bowel disease. Though rare, other causes of failure to respond to a gluten-free diet include lymphoma, ulcerative jejunitis, collagenous sprue, autoimmune enteropathy or refractory sprue."

Open Original Shared Link

You may want to speak to your doctor about some of the above Celiac-associated conditions (along with others).

JulesH Rookie
Jules......how did your tests go today?

Judy

My doctor's initial reaction was that there's nothing there "that needs to be dealt with right now" (whatever that means ;) ) but should have a full report next week, when we'll discuss what to do next. Thanks for your concern!

Judyin Philly Enthusiast
My doctor's initial reaction was that there's nothing there "that needs to be dealt with right now" (whatever that means ;) ) but should have a full report next week, when we'll discuss what to do next. Thanks for your concern!

KEY IS 'DEAL WITH RIGHT NOW' :ph34r: ............HANG AROUND FOLKS FOR THE DETAILS.....OMG THESE DRS............

WELL KEEP US POSTED OK ......................WE'LL WAIT WITH YA!

JulesH Rookie
KEY IS 'DEAL WITH RIGHT NOW' :ph34r: ............HANG AROUND FOLKS FOR THE DETAILS.....OMG THESE DRS............

WELL KEEP US POSTED OK ......................WE'LL WAIT WITH YA!

Well, when I saw him, he laughed when I asked why he had said "right now." I had him go through all the reports with me and there was nothing. He just likes to torture me apparently. :rolleyes:

But I really do love this guy. He doesn't want to drop it until we know for sure what's wrong (which is how I got the diagnosis for celiac in the first place -- any other doctor would've just said "Oh, you're female, so you're anemic. The end."), so he's sending me for more testing, since he's now localized my pain to possibly my stomach, rather than my large intestines. As soon as I work out whether the insurance requires me to see a GI before I do a barium swallow, I'll be able to make the appointment.

  • 1 month later...
silika Newbie
FYI:

"Q: Are there some celiacs who do not respond to the gluten-free diet?

A few patients have a poor clinical and/or histologic (biopsy) response to the diet. An important step in assessing patients who are non-responders is to confirm the diagnosis of celiac disease by review of the original biopsy, preferably by an expert gastrointestinal pathologist. However, the most common cause of a poor response is continued gluten ingestion, which may be intentional or unintentional.

An intolerance to other foods, such as lactose and fructose or soy can be a reason for lack of improvement. Some non-responders may have reversible pancreatic insufficiency or bacterial overgrowth, requiring treatment. Colonoscopy might indicate other causes of the failure to respond, such as microscopic colitis or inflammatory bowel disease. Though rare, other causes of failure to respond to a gluten-free diet include lymphoma, ulcerative jejunitis, collagenous sprue, autoimmune enteropathy or refractory sprue."

Open Original Shared Link

You may want to speak to your doctor about some of the above Celiac-associated conditions (along with others).

Really great answer: celiac's is often not as easy as eliminating gluten... it certainly has not been for me. It is getting to the point that I just about cannot eat anything any more! But I am not losing weight b/c I basically can't move enough to maintain a metabolism! Still trying to figure it out...

itchygirl Newbie

My "IBS" turned out to be sphincter of oddi dysfunction and chronic pancreatitis. Thank goodness for informed doctors at major medical centers! My aunt's "IBS" was ovarian cancer, and she died. :(

gfp Enthusiast
IBS is the number one misdiagnosis for Celiac. It is a garbage can diagnosis for when the doc does not know why you are having stomach issues.

I have yet to see a decent definition of IBS. It seems to shift with the seasons and moon cycles as far as I can tell.

I think its just an acronym doctors use for I'm Bamboozled Sorry ...

I think most cases it just means they don't have a clue and won't admit it. Calling it something makes it sound like they know what it is I guess.

I'm with the others that a primary reason for non improvement after an initial stage is often due to other intolerances than gluten.

I would also hazard a guess that many cases of IBS wil turn out to be other food intolerances noone has come up with a test for yet.

one related aspect to consider is the gluten-free diet can make us change what we eat quite significantly. Certain 'food's' such as Soya should probably never be eaten as a source of actual food but we get classed with the 'healthfood' freaks who will eat anytihng unconventional so long as it sounds exotic and we end up eating more of it just because its easier to buy gluten-free that way in a sort of catch-22.

I'm not fanatical about not eating Soya but I do try and limit it to an absolute minimum, likewise I TRY and limit my diary intake

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. - asaT replied to Scott Adams's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      45

      Supplements for those Diagnosed with Celiac Disease

    2. - par18 replied to Woodster991's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      9

      Is it gluten?

    3. - SilkieFairy replied to SilkieFairy's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      IBS-D vs Celiac

    4. - par18 replied to SilkieFairy's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      IBS-D vs Celiac

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

    • Total Members
      133,340
    • Most Online (within 30 mins)
      7,748

    Abbyyoung417
    Newest Member
    Abbyyoung417
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • asaT
      I was undiagnosed for decades. My ferritin when checked in 2003 was 3. It never went above 10 in the next 20 years. I was just told to "take iron". I finally requested the TTgIgA test in 2023 when I was well and truly done with the chronic fatigue and feeling awful. My numbers were off the charts on the whole panel.  they offered me an endoscopic biopsy 3 months later, but that i would need to continue eating gluten for it to be accurate. so i quit eating gluten and my intestine had healed by the time i had the biopsy (i'm guessing??). Why else would my TTgIgA be so high if not celiacs? Anyway, your ferritin will rise as your intestine heals and take HEME iron (brand 4 arrows). I took 20mg of this with vitamin c and lactoferrin and my ferritin went up, now sits around 35.  you will feel dramatically better getting your ferritin up, and you can do it orally with the right supplements. I wouldn't get an infusion, you will get as good or better results taking heme iron/vc/lf.  
    • par18
      Scott, I agree with everything you said except the term "false negative". It should be a "true negative" just plain negative. I actually looked up true/false negative/positive as it pertains to testing. The term "false negative" would be correct if you are positive (have anti-bodies) and the test did not pick them up. That would be a problem with the "test" itself. If you were gluten-free and got tested, you more than likely would test "true" negative or just negative. This means that the gluten-free diet is working and no anti-bodies should be present. I know it sounds confusing and if you don't agree feel free to respond. 
    • SilkieFairy
      I realized it is actually important to get an official diagnosis because then insurance can cover bone density testing and other lab work to see if any further damage has been done because of it. Also, if hospitalized for whatever reason, I have the right to gluten-free food if I am officially celiac. I guess it gives me some legal protections. Plus, I have 4 kids, and I really want to know. If I really do have it then they may have increased risk. 
    • par18
      Been off this forum for years. Is it that important that you get an official diagnosis of something? It appears like you had a trigger (wheat, gluten, whatever) and removing it has resolved your symptom. I can't speak for you, but I had known what my trigger was (gluten) years before my diagnosis I would just stay gluten-free and get on with my symptom free condition. I was diagnosed over 20 years ago and have been symptom free only excluding wheat, rye and barley. I tolerate all naturally gluten free whole foods including things like beans which actually helps to form the stools. 
    • trents
      No coincidence. Recent revisions to gluten challenge guidelines call for the daily consumption of at least 10g of gluten (about the amount in 4-6 slices of wheat bread) for a minimum of 3 weeks. If possible, I would extend that two weeks to ensure valid testing.
×
×
  • 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.