Wondering If I Might Be Glutin Intolerant....

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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

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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

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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


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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

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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 :)

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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.

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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!

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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.

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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.

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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.


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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

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    1. Toft M, Dietrichs E. Aggravated stuttering following subthalamic deep brain stimulation in Parkinson’s disease--two cases. BMC Neurol. 2011 Apr 8;11:44.
    2. Tani T, Sakai Y. Stuttering after right cerebellar infarction: a case study. J Fluency Disord. 2010 Jun;35(2):141-5. Epub 2010 Mar 15.
    3. Lundgren K, Helm-Estabrooks N, Klein R. Stuttering Following Acquired Brain Damage: A Review of the Literature. J Neurolinguistics. 2010 Sep 1;23(5):447-454.
    4. Jäncke L, Hänggi J, Steinmetz H. Morphological brain differences between adult stutterers and non-stutterers. BMC Neurol. 2004 Dec 10;4(1):23.
    5. Kell CA, Neumann K, von Kriegstein K, Posenenske C, von Gudenberg AW, Euler H, Giraud AL. How the brain repairs stuttering. Brain. 2009 Oct;132(Pt 10):2747-60. Epub 2009 Aug 26.
    6. Galantucci S, Tartaglia MC, Wilson SM, Henry ML, Filippi M, Agosta F, Dronkers NF, Henry RG, Ogar JM, Miller BL, Gorno-Tempini ML. White matter damage in primary progressive aphasias: a diffusion tensor tractography study. Brain. 2011 Jun 11.
    7. Lundgren K, Helm-Estabrooks N, Klein R. Stuttering Following Acquired Brain Damage: A Review of the Literature. J Neurolinguistics. 2010 Sep 1;23(5):447-454.
    8. [No authors listed] Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 43-1988. A 52-year-old man with persistent watery diarrhea and aphasia. N Engl J Med. 1988 Oct 27;319(17):1139-48
    9. Molteni N, Bardella MT, Baldassarri AR, Bianchi PA. Celiac disease associated with epilepsy and intracranial calcifications: report of two patients. Am J Gastroenterol. 1988 Sep;83(9):992-4.
    10. http://ezinearticles.com/?Food-Allergy-and-Stuttering-Link&id=1235725 
    11. http://www.craig.copperleife.com/health/stuttering_allergies.htm 
    12. https://www.celiac.com/forums/topic/73362-any-help-is-appreciated/
    13. Ford RP. The gluten syndrome: a neurological disease. Med Hypotheses. 2009 Sep;73(3):438-40. Epub 2009 Apr 29.
    14. Hadjivassiliou M, Gibson A, Davies-Jones GA, Lobo AJ, Stephenson TJ, Milford-Ward A. Does cryptic gluten sensitivity play a part in neurological illness? Lancet. 1996 Feb 10;347(8998):369-71.