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Is This Celiac Disease Or Gluten Intolerance Or Something Else?


Tidings

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Tidings Explorer

Hello folks,

Just found this helpful site and would like to post a brief description of my situation and ask your opinion as to whether this sounds like Celiac disease, Gluten intolerance, or something else...

Quick history:

Developed C.F.S. (chronic fatigue syndrome) over two decades ago and have had many health problems ever since, especially digestive tract troubles. About ten years ago, on a flight across country, airlines offered a gluten-free meal, so I decided to try it, and during my ten-day vacation, I avoided all wheat flour and the like. Noticed immediately that the "midriff bulge" disappeared! Seemed to feel better during this dietary experiment, but soon went back onto gluten.

In recent years, have "experimented" with a gluten-free diet, because it seemed like I could not digest white flour (pizza, pastries, and so on) and always had clogged intestines whenever I ate things like pizza or shortbread, etc. After many bouts with G.I. troubles and pain, decided about three years ago to just go GLUTEN FREE and see what would happen. Have been MOSTLY gluten free ever since, but do once in a while "fall off wagon" with a pizza or dessert containing gluten. Recently (over the past month or so) had pizza and a carrot cupcake a time or two, and have had EXTREME PAIN and clogged intestines and swollen abdomen and soreness in midregion. Had always heard that Celiac Testing would be inconclusive if you have been off gluten for a long while, so had not been tested.

Test Results:

Recently needed to have other bloodwork done, partly because of all this PAIN & DYSFUNCTION of late, so I asked Doctor to add the Celiac Panel testing, realizing the results would probably be negative and not tell much. Just got the test results back, which were:

Endomysical Antibody IgA - Negative

t-Transglutaminase (tTG) IgA - 1 (Negative 0 - 3)

Immunoglobulin A, Qn, Serum - 526 High - mg/dL Range: 70-400 <- What does this test mean?

Given the above, does it appear that I DO or DO NOT have Celiac disease, or Gluten Intolerance; or are these tests inconclusive because of avoiding gluten for a long time, and then only eating gluten sporadically? Hope somebody can help clarify things, as this is all very confusing.

Are there other tests that would make my situation more clear, or is this enough, along with all my side-effects from eating gluten, to accept that my condition really is Celiac disease and that I have to be on a permanent gluten-free diet?

Other Symptoms/Conditions:

*Often have EXTREMELY ITCHY Skin, especially head, back and legs

*Severe Insomnia (ever since contracting C.F.S.)

*Hair loss

*High Blood Pressure

*Glaucoma

*Many food sensitivities

*Extreme Fatigue

*Heart Arrhythmias, including Atrial Fibrillation

P.S. The doctor, upon seeing these results, said "You might want to avoid flour..." ???

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Tidings Explorer

Hi again,

It's nice to see the "84 Views" on my question, but disappointing to see no Replies yet.

Have to see doctor (who seems to know little to nothing about Celiac) again on Wednesday of this week and am hoping for some input on my above questions from the Celiac 'experts' on this forum. :-)

P.S. Hope this question didn't get posted in the wrong thread. Looking forward to hearing from some of you. Cheers--and have a nonglutenized day!

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Dixiebell Contributor

I am not positive what that test is for but I have heard that you need to be eating four slices of bread a day for several weeks before the blood tests and biopsy.

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Lisa Mentor

Hello folks,

Just found this helpful site and would like to post a brief description of my situation and ask your opinion as to whether this sounds like Celiac disease, Gluten intolerance, or something else...

Quick history:

Developed C.F.S. (chronic fatigue syndrome) over two decades ago and have had many health problems ever since, especially digestive tract troubles. About ten years ago, on a flight across country, airlines offered a gluten-free meal, so I decided to try it, and during my ten-day vacation, I avoided all wheat flour and the like. Noticed immediately that the "midriff bulge" disappeared! Seemed to feel better during this dietary experiment, but soon went back onto gluten.

In recent years, have "experimented" with a gluten-free diet, because it seemed like I could not digest white flour (pizza, pastries, and so on) and always had clogged intestines whenever I ate things like pizza or shortbread, etc. After many bouts with G.I. troubles and pain, decided about three years ago to just go GLUTEN FREE and see what would happen. Have been MOSTLY gluten free ever since, but do once in a while "fall off wagon" with a pizza or dessert containing gluten. Recently (over the past month or so) had pizza and a carrot cupcake a time or two, and have had EXTREME PAIN and clogged intestines and swollen abdomen and soreness in midregion. Had always heard that Celiac Testing would be inconclusive if you have been off gluten for a long while, so had not been tested.

Test Results:

Recently needed to have other bloodwork done, partly because of all this PAIN & DYSFUNCTION of late, so I asked Doctor to add the Celiac Panel testing, realizing the results would probably be negative and not tell much. Just got the test results back, which were:

Endomysical Antibody IgA - Negative

t-Transglutaminase (tTG) IgA - 1 (Negative 0 - 3)

Immunoglobulin A, Qn, Serum - 526 High - mg/dL Range: 70-400 <- What does this test mean?

Given the above, does it appear that I DO or DO NOT have Celiac disease, or Gluten Intolerance; or are these tests inconclusive because of avoiding gluten for a long time, and then only eating gluten sporadically? Hope somebody can help clarify things, as this is all very confusing.

Are there other tests that would make my situation more clear, or is this enough, along with all my side-effects from eating gluten, to accept that my condition really is Celiac disease and that I have to be on a permanent gluten-free diet?

Other Symptoms/Conditions:

*Often have EXTREMELY ITCHY Skin, especially head, back and legs

*Severe Insomnia (ever since contracting C.F.S.)

*Hair loss

*High Blood Pressure

*Glaucoma

*Many food sensitivities

*Extreme Fatigue

*Heart Arrhythmias, including Atrial Fibrillation

P.S. The doctor, upon seeing these results, said "You might want to avoid flour..." ???

Sorry for the delay. Weekends are often slow around here.

Here is some information regarding testing:

Open Original Shared Link

Gluten intolerance is offers a wide spectrum, with Celiac Disease as the as the autoimmune relation.

Many of your described symptoms correlate with the over 200 symptoms associated with Celiac, and it's associated illnesses.

With your partial gluten free tenure, it would be a possibility that your blood work would not be accurate enough for Celiac testing.

You may or may not have Celiac Disease, but it appears clear that you do have an issue with gluten.

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Tidings Explorer

Hi Lisa,

Thanks so much for replying. You said, "You may or may not have Celiac Disease, but it appears clear that you do have an issue with gluten." Boy, is that an understatement! LOL.

Have a feeling that more testing will be required for any solid diagnosis. Having the test result for the "Immunoglobulin A Serum" on the HIGH side is one thing that's confusing and there does not seem to be much info online about it. If anybody knows more precisely "what" it means to have a HIGH Immunoglobulin A Serum count, please advise. (i.e., Is this "Immunoglobulin A" referring solely to anti-gliadin antibodies or just an indication that there are lots of antibodies circulating in the blood that could be a reaction to other things instead of or as well as gluten?) (Apparently, high levels of Immunoglobulin A could also indicate kidney disease?)

Thanks also for the link to the University of Chicago Celiac Disease Center site. It has some very informative sections and it is inspiring that they're working so hard to educate and help folks with Celiac. It's also great that they have a Celiac Hotline: 773-702-7593.

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Tidings Explorer

I am not positive what that test is for but I have heard that you need to be eating four slices of bread a day for several weeks before the blood tests and biopsy.

Hi Dixiebell,

Wow--that's a lot of gluten! Based on how sensitive my innards seem to be toward gluten, don't think I'd make it past the first or second day of overindulging on gluten like that! (I'd definitely make it Pizza or Carrot Cake, instead of boring Bread, though! LOL)

It seems sort of crazy that we have to "repollute" ourselves with gluten, just to "prove" we have a problem with it. (Sort of like hitting your head with a hammer just to enjoy how good it feels when you stop!) Sigh...

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Marz Enthusiast

If anybody knows more precisely "what" it means to have a HIGH Immunoglobulin A Serum count, please advise. (i.e., Is this "Immunoglobulin A" referring solely to anti-gliadin antibodies or just an indication that there are lots of antibodies circulating in the blood that could be a reaction to other things instead of or as well as gluten?) (Apparently, high levels of Immunoglobulin A could also indicate kidney disease?)

Hi there,

Can't really say what a high result means, but the total IgA test you refer to is usually just done to check if you have a IgA deficiency, which would invalidate the other IgA tests. I don't think a high level is cause for concern, but check with your doctor when you see him :) Your other tests were negative, which is either because you don't have "classic" celiac disease, or you've been gluten-free for too long and your antibodies are too low to pick up.

By the way, lots of gluten-intolerant people get negative blood results, and still maintain a 100% gluten free diet. There are some theories that seronegative gluten intolerance (negative blood tests), is just "baby" celiac waiting to be activated. In other words, eat gluten at your own risk, you might develop full blown celiac (plus the other auto-immune problems that come with it) later on.

I'd say you've had a good result cutting gluten out, you should stick with the diet if it works for you :)

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ToriMartin Apprentice

I wish I could help but I'm not any help here... I seem to be asking more questions than anything.

I have always been allergic to Wheat Starch & Gluten. My worst problems have been over the last 12 years & getting worst. Hair loss, muscle & joint soreness, the Brain Fog is the worst! Weight Gain, fatigue, & lots more. I have blamed it on being Hypothyroid but recently have figured out that the Thyroid is probably a cause of the Gluten.

I asked the other day if it was Gluten Intolerance or Celiac... Still not sure... But, no matter what I'm staying away from gluten! I have also found that I can't have milk products, corn, avocado & possibly Garlic powder, testing that one... You really should do like I did... Only Veggies & meat for a week. Introduce other foods one at a time & see what happens. I notice I get bloated & IBS the next morning... Avacado gives me sinus pressure & a headache.

I'm far from being an expert... But if I were you I would stay 100% away from Gluten... It's just not worth it...

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IngridBeth Apprentice

I'm pretty new at this myself being only about 5 weeks gluten free, but I can tell you that

First, your symptoms sound a lot like mine (Fibromyaglia diagnosis in my case, high bp, etc.)

Second, my doctor acknowledged that blood tests can be misleading and based on a number of other factors, he diagnosed me with "probably Celiac but certainly gluten intolerance." In other words, I can't eat gluten either way. However many of my FM symptoms and a few blood test results that WERE "abnormal" makes him feel that Celiac is more likely.

I know it helps to have a diagnosis, but at least your doctor is pointing you in the right direciton, no? Good luck!

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bincongo Contributor

I have heard that the only certain way to diagnose Celiac is with a biopsy of the small intestine that is done with an endoscopy but I don't think doctors do this on a routine basis. I was diagnosed by biopsy but had it done for an unrelated problem. I guess in a way I feel blessed that I was "accidently" diagnosed because in spite of symptoms I thought it was just old age coming on.

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Skylark Collaborator

Endomysical Antibody IgA - Negative

t-Transglutaminase (tTG) IgA - 1 (Negative 0 - 3)

Immunoglobulin A, Qn, Serum - 526 High - mg/dL Range: 70-400 <- What does this test mean?

Given the above, does it appear that I DO or DO NOT have Celiac disease, or Gluten Intolerance; or are these tests inconclusive because of avoiding gluten for a long time, and then only eating gluten sporadically? Hope somebody can help clarify things, as this is all very confusing.

You already seem to know the answer. :P The tests are inconclusive because you are not eating enough gluten. High IgA is associated with autoimmune diseases like lupus, rheumatoid arthritis, liver disease, or possibly multiple myeloma (which your doctor would have picked up so don't worry). Your chronic fatigue may have some autoimmune component to it.

Are there other tests that would make my situation more clear, or is this enough, along with all my side-effects from eating gluten, to accept that my condition really is Celiac disease and that I have to be on a permanent gluten-free diet?

It's really annoying, but there is no formal test for celiac disease for people not eating much gluten. All the tests look for antibodies and damage, and it takes a lot of gluten to get a positive result. If you must have a formal "celiac disease" diagnosis to be willing to avoid gluten, you're going to have to gluten challenge and retest. Celiac researchers say you have to eat the equivalent of 4 slices of bread a day for a month to have a chance of getting the antibodies. Even then, there is a 20% false negative rate.

You could try genetic testing. If you're DQ2 or DQ8 there is a better chance it's celiac. The genetic test is not diagnostic, though.

If the gluten challenge is too much to contemplate (as it was for me) it's probably safest to just eat as if you were celiac.

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Tidings Explorer

Thanks to all of you who have posted your thoughts in this thread. And yes, the thought of a "gluten challenge" does induce a certain amount of queasiness, based on recent SEVERE pain and problems after enjoying a carrot cupcake and, the week before, some pizza!

Have kept a journal for years that substantiates the growing suspicion (conviction?) that either wheat or gluten induces A LOT OF PAIN & PROBLEMS. It's just so hard to accept a future without pizza (somehow, it seems to be THE hardest gluten-laden food to relinquish!). However, last week we found a pizza that is "almost" as good as gluten-loaded pizza. Some of you may have already found and enjoyed it. It is by Glutino (their gluten-free breads are good, too); the one I tried was their "spinach and feta" model. I added some gluten-free pizza sauce, mushrooms and black olives and sprinkled a bit of fennel (the spice that's in Italian sausage) on it, and then followed their baking instructions. Surprisingly good!--albeit a bit pricey. I think it cost $5-something at Whole Foods. It really was more like a pizza-COOKIE, based on the small size. But it was tasty, actually SATISFIED my craving for pizza, and the crust was NOT BAD AT ALL. So maybe there is hope! :-)

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Skylark Collaborator

Around here, there are at least four different restaurants where I can get gluten-free pizza. Have you looked for a celiac-friendly restaurant list in your area?

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ravenwoodglass Mentor

Thanks to all of you who have posted your thoughts in this thread. And yes, the thought of a "gluten challenge" does induce a certain amount of queasiness, based on recent SEVERE pain and problems after enjoying a carrot cupcake and, the week before, some pizza!

Have kept a journal for years that substantiates the growing suspicion (conviction?) that either wheat or gluten induces A LOT OF PAIN & PROBLEMS. It's just so hard to accept a future without pizza (somehow, it seems to be THE hardest gluten-laden food to relinquish!). However, last week we found a pizza that is "almost" as good as gluten-loaded pizza. Some of you may have already found and enjoyed it. It is by Glutino (their gluten-free breads are good, too); the one I tried was their "spinach and feta" model. I added some gluten-free pizza sauce, mushrooms and black olives and sprinkled a bit of fennel (the spice that's in Italian sausage) on it, and then followed their baking instructions. Surprisingly good!--albeit a bit pricey. I think it cost $5-something at Whole Foods. It really was more like a pizza-COOKIE, based on the small size. But it was tasty, actually SATISFIED my craving for pizza, and the crust was NOT BAD AT ALL. So maybe there is hope! :-)

I love pizza and have it about once a week. I get Kinnickinnick pizza crusts at a package of 4 for about 9 bucks. I add my own cheese and whatever toppings I want. The crusts are nice and much like the crusts I remember from my gluten days. If I am feeling like taking the time and want an awesome deep dish I get Gluten Free Pantry's French Bread mix and follow their directions to make it as a pizza crust. I usually chill it for a bit before I spread it. A real treat when I have time.

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Marz Enthusiast

It's just so hard to accept a future without pizza (somehow, it seems to be THE hardest gluten-laden food to relinquish!). However, last week we found a pizza that is "almost" as good as gluten-loaded pizza.

Since we don't have any ready-made gluten-free pizza crusts here, I just make my own from corn meal. Can make it either crispy by making the dough layer very thin, or slightly doughy. Tastes pretty good, and you can make up a whole batch, cook it up and freeze it for later.

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    • trents
      But if you have been off of wheat for a period of weeks/months leading up to the testing it will likely turn out to be negative for celiac disease, even if you actually have celiac disease. Given your symptoms when consuming gluten, we certainly understand your reluctance to undergo  the "gluten challenge" before testing but you need to understand that the testing may be a waste of time if you don't. What are you going to do if it is negative for celiac disease? Are you going to go back to merrily eating wheat/barley/rye products while living in pain and destroying your health? You will be in a conundrum. Do I or do I not? And you will likely have a difficult time being consistent with your diet. Celiac disease causes inflammation to the small bowel villous lining when gluten containing grains are consumed. This inflammation produces certain antibodies that can be detected in the blood after they reach a certain level, which takes weeks or months after the onset of the disease. If gluten is stopped or drastically reduced, the inflammation begins to decrease and so do the antibodies. Before long, their low levels are not detectable by testing and the antibody blood tests done for diagnosing celiac disease will be negative. Over time, this inflammation wears down the billions of microscopic, finger-like projections that make up the lining and form the nutrient absorbing layer of the small bowel where all the nutrition in our food is absorbed. As the villi bet worn down, vitamin and mineral deficiencies typically develop because absorption is compromised. An endoscopy with biopsy of the small bowel lining to microscopically examine this damage is usually the second stage of celiac disease diagnosis. However, when people cut out gluten or cut back on it significantly ahead of time before the biopsy is done, the villous lining has already experienced some healing and the microscopic examination may be negative or inconclusive. I'm not trying to tell you what to do I just want you to understand what the consequences of going gluten free ahead of testing are as far as test results go so that you will either not waste your time in having the tests done or will be prepared for negative test results and the impact that will have on your dietary decisions. And, who are these "consultants" you keep talking about and what are their qualifications? You are in the unenviable position that many who joint this forum have found themselves in. Namely, having begun a gluten free diet before getting a proper diagnosis but unwilling to enter into the gluten challenge for valid testing because of the severity of the symptoms it would cause them.
    • Zackery Brian
      I'm sorry to hear about the challenges you've been facing with your health. Dealing with celiac disease and multiple food sensitivities can indeed be overwhelming. Here are a few thoughts and suggestions based on your experience and the replies you've received: Confirming Diagnosis: It's great that your gastroenterologist confirmed your celiac disease diagnosis through additional tests. Understanding the specifics of your condition can help tailor your approach to managing it more effectively. Food Sensitivity Testing: While blood tests for food sensitivities can provide some insights, they may not always be completely accurate. As mentioned by others, false positives are common, and individual responses to specific foods can vary. Discussing your test results and symptoms with a healthcare professional knowledgeable about celiac disease and food sensitivities can help clarify your situation. Research and Education: Exploring conditions like Mast Cell Activation Syndrome (MCAS) and histamine intolerance could shed further light on your symptoms and provide additional avenues for managing your health. Gathering information from reliable sources and discussing your findings with your healthcare team can help you make informed decisions about your care. Dietary Management: Managing celiac disease and multiple food sensitivities can be challenging, but finding a balance that works for you is crucial. Working with a dietitian who specializes in celiac disease and food intolerances can help you develop a personalized dietary plan that meets your nutritional needs while minimizing symptoms. Stress Management: Chronic pain and health issues can take a toll on mental and emotional well-being. Finding healthy coping strategies to manage stress, such as mindfulness, relaxation techniques, or engaging in activities you enjoy, may help improve your overall quality of life. Remember, you're not alone in your journey, and seeking support from healthcare professionals, support groups, or online communities can provide valuable encouragement and guidance.
    • Fluka66
      Thank you very much for your reply. I hadn't heard of celiac disease but began to notice a pattern of pain. I've been on the floor more than once with agonising pain but this was always put down to another abdominal problem consequently I've been on a roundabout of backwards and forwards with another consultant for many years. I originally questioned this diagnosis but was assured it was the reason for my pain. Many years later the consultant gave up and I had a new GP. I started to cut out certain food types ,reading packets then really started to cut out wheat and went lactose free. After a month I reintroduced these in one meal and ended screaming in agony the tearing and bloating pain. With this info and a swollen lymph node in my neck I went back to the GP.  I have a referral now . I have also found out that acidic food is causing the terrible pain . My thoughts are this is irritating any ulcers. I'm hoping that after a decade the outlook isn't all bad. My blood test came back with a high marker but I didn't catch what it was. My GP and I have agreed that I won't go back on wheat just for the test due to the pain , my swollen lymph node and blood test results.  Trying to remain calm for the referral and perhaps needed to be more forceful all those years ago but I'm not assertive and consultants can be overwhelming. Many thanks for your reply . Wishing you all the best.
    • Moodiefoodie
      Wow! Fascinating info. Thanks so much! I really appreciate the guidance. @Spacepanther Over the years I have had rheumatologists do full lab work ups on me. They told me they had screened me for arthritis, lupus, and Lyme disease (all negative). In addition to joint pain and stiffness I had swelling in both knees that later moved to my elbow as well.  I also experience stiffness and pain in my neck and shoulders when it flares. I vomited fairly often growing up, but there wasn’t a real pattern to it and I didn’t know it wasn’t normal (thought people caught stomach viruses often).  I don’t usually have stomach symptoms immediately after eating gluten that I notice.  The only other joint condition I know of is fibromyalgia. Good luck! Hope you can get it figured out. I only assumed my joint symptoms were due to the celiac’s because it is under control for the most part on a gluten-free diet.  The rheumatologist also mentioned that some inflammatory/autoimmune diseases can be slow-moving and not detectable until they progress.
    • knitty kitty
      @Spacepanther, I found these articles about the connection between Celiac and joint pain. Musculoskeletal Complications of Celiac Disease: A Case-Based Review https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10201087/ And   Intestinal microbiome composition and its relation to joint pain and inflammation https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6814863/ And The gut microbiome-joint connection: implications in osteoarthritis https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6903327/ Sounds like it's time to change the diet to change the microbiome.
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