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

Wondering If I Might Be Glutin Intolerant....


TheCatWhisperer

Recommended Posts

TheCatWhisperer Newbie

Ok, so about 4 years ago I was "diagnosed" with IBS, that is, i started suffering from diarrhea, at first mild, then within months it was bad. My doc sent me for blood, urine & stool tests, all came back fine, then he sent me for a barium X-Ray, which came back fine (minus a few minor diverticuli). His diagnosis was IBS, that it was likely *caused* by stress and put me on Paxil & Imodium. So I lived with those pills for over 2 years. Eventually I got fed up with being on Paxil & feeling nothing and quit cold turkey, I was still on about 3 Imodium per day to keep the D from happening. (would still have "attacks" once in a while).

I switched doctors and he came to the same conclusion (no tests were done), and so I continued for another year or so. I recently (about a month ago) went to a different doc one day as my regular GP was not in, he listened to my story and almost immediately asked if I had tried a Lactose or Gluten free diet. Huh? So I tried them both, I cut lactose & gluten out of my diet for 3 weeks.

So after about 2 weeks I started feeling better, I was able to cut my Imodium down to 1 & 1/2 to 2 per day, and rarly felt pain or crampiness. The next step was to re0introduce both lactose & gluten (one at a time), and the lactose went fine, but the gluten was not bad, but I feel crampy and icky again (my Imodium is the same at about 2 per day).

What I'm wondering is what does it mean? (I can't get in to see the doctor for another two weeks, they are booked...) And what should I do next?

Is it possible that I have had Celiac Disease for over 3 years?

Could that be why I haven't seen a great change in my bowel habits, but have seen some?

Is it just possible that the change in foods was just better for my IBS and I do not have Celiac?

*confused & bewildered*

Oh, yeah, I'm 28, Male, never smoked, rarely ever drink, and am usually stressed.

Thanks for any ideas, comments or help you can give, I REALLY appreciate it :D


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



Celiac.com Sponsor (A8-M):



KaitiUSA Enthusiast

It is definitely possible to have celiac for a long period of time and not know about it. I think the average is 11 years until a diagnosis. You should get a full celiac panel to start with at the doctor. The full panel includes:

Anti-Gliadin (AGA) IgA

Anti-Gliadin (AGA) IgG

Anti-Endomysial (EMA) IgA

Anti-Tissue Transglutaminase (tTG) IgA

Total Serum IgA

The 3 most important are the tTG, EMA, and total serum IgA

A gene test may be helpful as well.

Make sure you are on gluten while the testing goes on because being gluten free can interfere with the test results.

Your symptoms sound like celiac but with celiac its hard because there is a broad range of symptoms and one does not even have to have any symptoms.

Celiac is commonly misdiagnosed for things like IBS.

Celiac can be triggered at any time in life. Mine was triggered by mono at age 15. My whole life prior I didn't have symptoms. Other things that can trigger celiac to activate are surgery,stress, bacterial &viral infections, etc.

Hope this helps you out a bit and good luck :D

TheCatWhisperer Newbie

KaitiUSA, actually, it helps quite a bit, and to think of it, i did have to rather major infections prior to coming down with the symptoms, on was a bad throat infection (they put me on a double dose of Amoxicillin). that double dosage caused me to become allergic to penicillin, and then the next infection (ear) they put me on something else, it was a few months later i came down with the diarrhea.

I should really mention this to my doc, as well as ask for those tests.

Thanks again soo much :D

/c

celiachap Apprentice

Like many people here, I was also misdiagnosed even after visiting numerous specialists - including gastroenterologists, TWO hematologists, and others.

After my own research pointed toward Celiac, I asked for the blood tests at a routine physical. Upon receiving the results, I went to a new endo in Feb., 2005 and got a small-intestine endoscopy w/biopsy. If your insurance covers these tests, it's probably best to get them.

Good luck

jenvan Collaborator

Christien--

How frustrating all this is for you, I'm sure! I would say there is definitely a good chance you have Celiac, and echo Kaiti--get tested! I was diagnosed with "IBS" about 13 years ago as well...and thought that was my problem, when it was always Celiac. I finally got my diagnosis this year ! Good luck to you--let us know what you find out.

PS--Love your name-CatWhisperer--I have a cat at home :)

stef-the-kicking-cuty Enthusiast

Hello CatWhisperer,

yes, it's possible, to have celiac for a long time and not know about it. As Kaiti already said, the average is 11 years. I'm also 28. I had pain for 7 years and I believe I had it before that also, just not triggered. A tooth surgery triggered the celiac symptoms with me. After that tooth surgery I also became allergic to aspirin. Known triggers of celiac can be stress or surgeries. You mentioned you had a lot of stress. Maybe that was it.

TheCatWhisperer Newbie

I want to thank you all for replying, it makes me feel much better, and I now have notes to take to my doctor and will hopefully get tested. My insurance is very good, so I should have no issues there (and I'm in Canada, so most of it is covered anyway).

Just on other question, how long (for those of you who got diarrhea form the Celiac) did it take for the D to "go away"? I'm just wondering, if it takes months, that is fine with me, I just want o stop relying in drugs like Imodium to treat it. (If indeed I am diagnosed with Celiac).

Thanks again, you all are great!


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



Celiac.com Sponsor (A8-M):



KaitiUSA Enthusiast

For me I did not have D with it but I had other symptoms. It varies from person to person for how long it takes for symptoms to go away. My symptoms got significantly better after 3 months but it was a few more months after that until I was back to normal. For some people they can feel better within days...for others it can take months...it depends on how much damage is done and so forth.

judy05 Apprentice

I had diarrhea when I got glutened, I think it took a week or two after I knew what the culprit was. My doc put me on fiber pills, Citrucel, he said they work on diarrhea and/or constipation.

psawyer Proficient

Hi, Christien,

I am also in Canada. Welcome to the forum. There are several other Canadians on here, but as far as I know we are the only two males. If there are any other Canadian guys active here, please make yourself known.

I'm just outside Toronto. Where are you?

BTW, cats rule the world. Humans only exist to serve them. We own a pet food and supply store. Two cats live at the store and tolerate our presence; four more occupy the house that we maintain for their benefit.

Peter

pixiegirl Enthusiast

Hi and welcome CatWhisperer! (ok I'm a dog person but I've had two wonderful cats in my life, Kitty Thom and Nana (who is male, don't ask about the name!)

About the D.... I have similar diagnoses to you IBS for 11 years and then found out its Celiac. However I still have some issues with the D.... when I first went gluten-free I was totally better in a couple of weeks, I didn't have the runs, life was wonderful.

Then back in April, I went to the panhandle of Florida for a week to visit my brother and was glutened, not just every day but virtually at every meal. Wow was I sick... I see why some people call D the runs.... anyhow... since then I've been totally gluten-free and yet I still have had the runs... I just can't stop them. Well like Judy my Dr. told me that fiber may help... so I'm using Metamucil the kind you mix in water (sheesh I hope its gluten-free, pretty sure it is), I was told it helps promote regularity... its not just for constipation, its for either problem.. C or D.

I started with just one dose a day.... (it really gives me gas, but it says your body adjusts) and now I'm up to the recommended dose on the package... 3 x per day and guess what... no D at all.

I'm still wondering why after I went totally gluten-free again the D didn't clear up on its own... but this has worked for me perfectly. I'm going to start to test other things... go dairy free for a while, soy free and see if I can identify other sensitivities.

Good luck, Susan

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. - Hmart replied to Hmart's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      2

      Is this celiac?

    2. - trents replied to Hmart's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      2

      Is this celiac?

    3. - klmgarland replied to klmgarland's topic in Dermatitis Herpetiformis
      10

      Help I’m cross contaminating myself,

    4. - DebJ14 replied to Jhona's topic in Introduce Yourself / Share Stuff
      30

      Does anyone here also have Afib

    5. - Hmart posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      2

      Is this celiac?


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,924
    • Most Online (within 30 mins)
      7,748

    Mckshane
    Newest Member
    Mckshane
    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

    • Hmart
      I was not taking any medications previous to this. I was a healthy 49 yo with some mild stomach discomfort. I noticed the onset of tinnitus earlier this year and I had Covid at the end of June. My first ‘flare-up’ with these symptoms was in August and I was eating gluten like normal. I had another flare-up in September and then got an upper endo at the end of September that showed possible celiac. My blood test came a week later. While I didn’t stop eating gluten before I had the blood test, I had cut back on food and gluten both. I had a flare-up with this symptoms after one week of gluten free but wasn’t being crazy careful. Then I had another flare-up this week. I think it might have been caused by Trader Joe’s baked tofu which I didn’t realize had wheat. But I don’t know if these flare-ups are caused by gluten or if there’s something else going on. I am food journaling and tracking all symptoms. I have lost 7 pounds in the last 10 days. 
    • trents
      Welcome to the forum, @Hmart! There are other medical conditions besides celiac disease that can cause villous atrophy as well as some medications and for some people, the dairy protein casein. So, your question is a valid one. Especially in view of the fact that your antibody testing was negative, though there are also some seronegative celiacs. So, do you get reactions every time you consume gluten? If you were to purposely consume a slice of bread would you be certain to develop the symptoms you describe?
    • klmgarland
    • DebJ14
      I only went on the multi vitamin AFTER a couple of year of high dose, targeted supplementation resolved most of my deficiencies.  I was on quite a cocktail of vitamins that was changed every 6 months as my deficiencies resolved.  Those that were determined to be genetic are still addressed with specific doses of those vitamins, minerals and amino acids. I have an update on my husband and his A Fib.  He ended up in the hospital in August 2025 when his A Fib would not convert.  He took the maximum dose of Flecainide allowed within a 24 hour period.  It was a nightmare experience!  They took him into the ER immediately.  They put in a line, drew blood, did an EKG and chest Xray all within minutes.  Never saw another human for 6 hours.  Never got any results, but obviously we could see he was still in A fib by watching the monitor.  They have the family sign up for text alerts at the ER desk.  So glad I did.  That is the only way we found out that he was being admitted.  About an hour after that text someone came to take him to his room on an observation floor.  We were there two hours before we saw another human being and believe it or not that was by zoom on the TV in the room.  It was admissions wanting to know his vaccine status and confirming his insurance, which we provided at the ER desk.  They said someone would be in and finally a nurse arrived.  He was told a hospitalist was in charge of his case.  Finally the NP for the hospitalist showed up and my husband literally blew his stack.  He got so angry and yelled at this poor woman, but it was exactly what he needed to convert himself to sinus rhythm while she was there.  They got an EKG machine and confirmed it.  She told him that they wanted to keep him overnight and would do an echo in the morning and they were concerned about a wound on his leg and wanted to do a doppler to make sure he did not have a DVT.  He agreed.  The echo showed everything fine, just as it was at his annual check up in June and there was no DVT.  A cardiologist finally showed up to discharge him and after reviewing his history said the A Fib was due to the Amoxicillan prescribed for his leg wound.  It both triggers A Fib and prevents the Flecainide from working.  His conversion coincided with the last dose of antibiotic getting out of his system.  So, make sure your PCP understands what antibiotics you can or cannot take if susceptible to A Fib.  This cardiologist (not his regular) wanted him on Metoprolol 25 mg and Pradaxa.  My husband told him that his cardiologist axed the idea of a beta blocker because his heart rate is already low.  Sure enough, it dropped to 42 on the Metoprolol and my husband felt horrible.  The pradaxa gave him a full body rash!  He went back to his cardiologist for follow up and his BP was fine and heart rate in the mid 50's.  He also axed the Pradaxa since my husband has low platelets, bruises easily and gets bloody noses just from Fish Oil  He suggested he take Black Cumin Seed Oil for inflammation.  He discovered that by taking the Black Seed oil, he can eat carbs and not go into A Fib, since it does such a good job of reducing inflammation.   Oh and I forgot to say the hospital bill was over $26,000.  Houston Methodist!  
    • Hmart
      The symptoms that led to my diagnosis were stomach pain, diarrhea, nausea, body/nerve tingling and burning and chills. It went away after about four days but led me to a gastro who did an upper endo and found I had marsh 3b. I did the blood test for celiac and it came back negative.  I have gone gluten free. In week 1 I had a flare-up that was similar to my original symptoms. I got more careful/serious. Now at the end of week 2 I had another flare-up. These symptoms seem to get more intense. My questions:  1. How do I know if I have celiac and not something else? 2. Are these symptoms what others experience from gluten?  When I have a flare-up it’s completely debilitating. Can’t sleep, can’t eat, can’t move. Body just shakes. I have lost 10 pounds since going gluten free in the last two weeks.
×
×
  • 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.