Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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 Celiac.com!
    eNewsletter
    Donate

No Celiac


Linda56

Recommended Posts

Linda56 Apprentice

I read this site off and on. I had the testing for celiacs. It was negative. Is there any other disease that can cause the symptoms of celiacs? I really identify with so many. I have diarreah alot. I have thought its lactose intolerance then thought I have irritable bowel. Was told years ago I had spastic bowels. When I have been able to diet I feel like I get much better. The thing is I have an inner ear disease that caused me to loose my balance. Which really can irritate my stomach and make me feel nauseous. I had the stomach thing before the ear problem or I would say the ear thing was causing it. I also have been told I have asthma that seems to come on from allergies. Last time I colored my hair I had an allergic reaction and now they want to put chemical on my back to try and find out what chemicals I am allergic to. I am not to keen on that as it can cause reactions. I have pernious anemia and get B-12 shots. Doctor was telling the pernious anemia and asthama are immune related. Its been suggested the ear thing is from an autoimmune reaction. I feel like my stomach throws me into vertigo sometimes if I eat the wrong thing or to much. Right now I am going through a thing where I can't eat much at one time or I will feel like I am going to faint. And yet if I don't eat feel I am going to faint. Can't seem to get a handle on what I need to feel better. I can't tell what make me feel the worst. I can say right now I only want to eat potatoes boiled or baked. My lower stomach I guess intestinal area feels bloated and like the muscles are week. Feels like I have been exercising my stomach but I haven't. I am not thin or look like I have any eating problem. Does any of these sound familar to anyone. Thanks for letting me post this and any thoughts.

Linda

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



Guest schmenge

Sorry that you or the docs can't identify what is wrong. How do you know you do not have Celiac? Blood tests are NOT conclusive, but a biopsy is. Many Celiacs are misdiagnosed with IBS. Has this been considered? If you have not already done so, you could try going gluten-free anyway. It can't hurt, and if your symptoms begin to abate..........

Link to comment
Share on other sites
Rikki Tikki Explorer

I agree with Mark Linda. The blood test is going to show negative if you have been off gluten for even a short time before the blood work is done. If you feel better going gluten free then that's the way to go.

Many people on the board also talk about a lab they use, I think entrolab or something, you might want to use them. The correct name should be posted here somewhere.

Link to comment
Share on other sites
tarnalberry Community Regular
...

I had the testing for celiacs. It was negative. Is there any other disease that can cause the symptoms of celiacs?...

I have diarreah alot. ...

When I have been able to diet I feel like I get much better. ...

I also have been told I have asthma that seems to come on from allergies. ...

I have pernious anemia and get B-12 shots. ...

Its been suggested the ear thing is from an autoimmune reaction.

I feel like my stomach throws me into vertigo sometimes if I eat the wrong thing or to much. Right now I am going through a thing where I can't eat much at one time or I will feel like I am going to faint. And yet if I don't eat feel I am going to faint. ... I can say right now I only want to eat potatoes boiled or baked. ...

I have two thoughts:

First:

Your symptoms do sound similar to celiac. I strongly dislike when people think that any and everything is celiac, because it isn't. But 1 in 100 people in the general population, and something like 1 in 50 people who present symptoms have it. And you present symptoms! Particularly, you present a number of 'common' symptoms, red-flags if you will: diarreah, anemia, an additional autoimmune condition (possibly), and the dizziness that many people get after eating gluten.

So, my question is - what were your tests? Did you have the full panel of Total IgA, Anti-gliandin IgA, Anti-gliandin IgG, tTg and EMA? If you just had the Anti-gliandin IgA and tTg, and those two came back worthless, then your doctor did worthless testing. (Bascially, those two tests coming back negative tell you the equivalent of "you're glass has less than two ounces of water in it" and "your intestines are probably not totally ripped to shreds". The problem is, many people with celiac disease are IgA deficient - in my analogy, it means that their glasses can only hold one ounce anyway, so no test will ever show them holding two ounces of water. And the tTg relies on the intestines being damaged at a level that takes years in some people.)

If you don't know what tests were run, or what the actual results were, please do call your doctor and get those results. The new medical record laws guarantee you access to your records, so they have to give you the results.

Additionally, the fact that you improved on a gluten-free diet is THE MOST IMPORTANT test result you can have. Yes, the dietary challenge is a test, and yes, your response on it is a valid test result. Don't ignore such an important result. Listening to your body is always vital.

Two:

Some of what you describe sounds like a blood sugar problem. It may or may not be such a thing, but it's just one of the possibilities. It could be that the asthma is separate (allergy triggered asthma is very common - I had it for years before I developed celiac disease, which I believe was triggered by a nine month battle with various respiratory infections for me), as could the anemia (particuarly depending on your genetics and diet and so on). I think it's less likely than the first option, of course, but it can cause the dizziness and stomach problems you're describing. Particularly if you're finding that things like potatoes are causing a problem.

Link to comment
Share on other sites
Guest nini

you may have "non Celiac Gluten intolerance" which doesn't show up in any testing, but if you go on the gluten-free diet and have a positive response to it, then you have your answer. You may have multiple food intolerances as well.

To me it sounds like Celiac, and probably is. Just because the testing was negative, doesn't mean a thing. The testing is all subjective. The most reliable test is quite simply, how does your body respond to the diet. Since you've already done blood testing, I wouldn't reccommend the biopsy, I would reccommend going gluten-free immediately and give your body a chance to heal. It can take 6 months to 2 years (average) for true healing to start, but you might start noticing improvements after a few days or weeks...

good luck and feel free to hang around this board and ask questions

you asked if other diseases can cause the same symptoms and to answer with my opinion, there are some other things that are related but have also shown that they improve on the gluten-free diet as well, so my first choice would be to try dietary changes and see if it works... according to most Dr.s they will dx IBS, Chrons, Colitis, and other things, and just treat the symptoms with drugs... OR you can see if gluten is the underlying CAUSE and treat the cause and not the symptoms. And again, the best way to determine that is the diet.

Link to comment
Share on other sites
Ursa Major Collaborator

Hi Linda, and welcome to this board. I agree with the others, you sound like you have celiac disease, despite the negative tests. They certainly can be wrong. I also encourage you to try the gluten-free diet. You may also have other intolerances. Potatoes will cause bloating and diarrhea for me, too. You may try staying away from gluten, dairy and nightshades and see how you feel (give it at least two weeks to see if it works).

After a while (a month maybe) you do a challenge to see what happens. Eat some bread and see if you react. Wait for two weeks to rule out delayed reactions. If you reacted eliminate that food again, and try dairy for instance. Two weeks later try potato.

Many people with celiac disease also react to soy and/or corn. Since your doctor isn't much help, you may have to figure it out yourself. It can take a while, but is possible.

Link to comment
Share on other sites
Linda56 Apprentice

Gee thanks alot for all the responses. I think I will make an appt to see my records at the clinic I go to. Just to see the exact name of the testing that was done. I did have an IGG, IGA, IGM testing I think the IGG and IGM were negative but the IGA was positive. The doctor said that had to do with mucus membranes. But then he said he was doing another test for celiac he did and it was negative.

Trying gluten free seems like the simplest way to go and see what happens. I eat a lot of rice as it doesn't usually bother me. I haven't connected potatoes with anything so I am not sure. The only bread type thing I feel for sure bothers me is rye or pumpernickel bread. I eat oatmeal but feel like it bothers me. But then oatmeal has so much fiber I thought maybe that is what I feel. I really can't tolerate raw vegetables very well. I don't mean just in a stomach sense but just a strange feeling. Especially cantalope, bananas or anything with the least bit greenness to it. Or if I get any rine like from water melon. I read one time a person can be allergic to vegetables or fruit but not neccessarly that they can't eat them. I can't drink coffee or any kind decaf or regular. Dieting before I mainly ate rice, pinto beans, turkey, oinons and that was about it. I get very ill if I eat at restaurants there is a lot of salt, msg and fat in most food. I am just rattling on I don't expect you all to neccessairily reply to it. Just kind of thinking and putting it down. I will check out the entrolab again. I beleive I looked at it before. I had read a post some people weren't sure it was dependable so I hadn't used it. I was hoping after I got situated with getting the B-12 up I might get back to my doctor. I had mentioned to him a couple times about my stomach and he said he would send me to a gastroenterologist for a colonoscopy. I think I will try and find a book I can read about celiac. I have trouble keeping stuff recorded in my brain. Having a book I can look back to always helps me. Thanks everyone.

Linda

Hi Linda, and welcome to this board. I agree with the others, you sound like you have celiac disease, despite the negative tests. They certainly can be wrong. I also encourage you to try the gluten-free diet. You may also have other intolerances. Potatoes will cause bloating and diarrhea for me, too. You may try staying away from gluten, dairy and nightshades and see how you feel (give it at least two weeks to see if it works).

After a while (a month maybe) you do a challenge to see what happens. Eat some bread and see if you react. Wait for two weeks to rule out delayed reactions. If you reacted eliminate that food again, and try dairy for instance. Two weeks later try potato.

Many people with celiac disease also react to soy and/or corn. Since your doctor isn't much help, you may have to figure it out yourself. It can take a while, but is possible.

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



tarnalberry Community Regular

You don't have to make an appointment to see your records. Ask them to mail you a copy (or fax you a copy).

Link to comment
Share on other sites
KaitiUSA Enthusiast

What blood tests did you get done? Some are more accurate. There should be 5 tests done...also a gene test is never a bad idea. Also, as far as a biopsy goes...a biopsy can rule celiac in but not out. You could very well have celiac still even with negative testing.

Link to comment
Share on other sites

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. - BluegrassCeliac replied to lasthope2024's topic in Food Intolerance & Leaky Gut
      7

      This forum might be the last hope I have in my life. Please I beg you

    2. - Scott Adams replied to Nacina's topic in Related Issues & Disorders
      1

      14 year old with Celiac & EOE still suffering...

    3. - Nacina posted a topic in Related Issues & Disorders
      1

      14 year old with Celiac & EOE still suffering...

    4. - trents replied to Fluka66's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      5

      Waiting for urgent referral.

    5. - Fluka66 replied to Fluka66's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      5

      Waiting for urgent referral.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      121,067
    • Most Online (within 30 mins)
      7,748

    myneckmybackmyceliac
    Newest Member
    myneckmybackmyceliac
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • BluegrassCeliac
      Hi,   Not saying Thiamine (B1) couldn't be an issue as well, but Mg was definitely the cause of my problems. It's the only thing that worked. I supplemented with B vitamins, but that didn't change anything, in fact they made me sick. Mg stopped all my muscle pain (HCTZ) within a few months and fixed all the intestinal problems HCTZ caused as well. Mom has an allergy to some sulfa drugs (IgG Celiac too), but I don't think I've ever taken them. Mg boosted my energy as well. It solved a lot of problems. I take 1000mg MgO a day with no problems. I boost absorption with Vitamin D. Some people can't take MgO,  like mom, she takes Mg Glycinate. It's one of those things that someone has try and find the right form for themselves. Everyone's different. Mg deficiency can cause anxiety and is a treatment for it. A pharmacist gave me a list of drugs years ago that cause Mg deficiency: PPIs, H2 bockers, HCTZ, some beta blockers (metoprolol which I've taken -- horrible side effects), some anti-anxiety meds too were on it. I posted because I saw he was an IgG celiac. He's the first one I've seen in 20 years, other than my family. We're rare. All the celiacs I've met are IgA. Finding healthcare is a nightmare. Just trying to help. B  
    • Scott Adams
      It sounds like you've been through a lot with your son's health journey, and it's understandable that you're seeking answers and solutions. Given the complexity of his symptoms and medical history, it might be beneficial to explore a few avenues: Encourage your son to keep a detailed journal of his symptoms, including when they occur, their severity, any triggers or patterns, and how they impact his daily life. This information can be valuable during medical consultations and may help identify correlations or trends. Consider seeking opinions from specialized medical centers or academic hospitals that have multidisciplinary teams specializing in gastrointestinal disorders, especially those related to Celiac disease and Eosinophilic Esophagitis (EOE). These centers often have experts who deal with complex cases and can offer a comprehensive evaluation. Since you've already explored alternative medicine with a nutrition response doctor and a gut detox diet, you may want to consider consulting a functional medicine practitioner. They take a holistic approach to health, looking at underlying causes and imbalances that may contribute to symptoms. Given his low vitamin D levels and other nutritional markers, a thorough nutritional assessment by a registered dietitian or nutritionist specializing in gastrointestinal health could provide insights into any deficiencies or dietary adjustments that might help alleviate symptoms. In addition to routine tests, consider asking about more specialized tests that may not be part of standard screenings. These could include comprehensive stool analyses, food intolerance testing, allergy panels, or advanced imaging studies to assess gut health.
    • Nacina
      Hello, I am a 45 year old mom, who was diagnosed at 29 with Celiac. My now 14 year old son was diagnosed just before his 4th birthday. Needless to say, we are old pros with the diet. He was experiencing some issues, overall health took a major plummet a year ago, and through a bit of work, was diagnosed with EOE. Tried diet alone, but his follow up endoscopy didn't show the improvements his DR. wanted to see, so I tried the medication. (Steroid). He became extremely backed up, and they had him taking Miralax daily. His health plummeted. He is a straight A honor's 8th grader who plays club soccer very competitively. His health continued to decline and at 13 had a colonoscopy and another upper gi. (He was still compacted even with the prep). I finally pulled him off all meds and mira lax, after reading much negative literature online, and put him on a gut detox diet and took him to a nutrition response dr. Finally things have improved. However...over a year later and he is having relapse stomach pain, debilitating stomach pain. Missing a day of school a week, to three this week. This is where we downward spiral with him. He says it doesn't feel the same as when he has gotten backed up before. He is eating prunes, taking his supplements, drinking water...all of the things. Yet, he is feeling horrible. Pain is abdomen, headache, lethargy, diarrhea . He is on a strict gluten dairy, egg free diet. He has adapted well in regards to diet. But I feel like we are missing something here. He is too active, too outgoing to be feeling sick all of the time. His Bilirubin is constantly high. His white blood count always runs slightly low. His vitamin D was very low last time he ran tests, (last month) when he was sick for a week. His celiac markers show negative, so it isn't that. His last endoscopy showed no Eosinaphils in his esophagus.  I have taken him to multiple Ped. Gastro specialists. They run tests, and we get zero answers. I meticulously go through labs, hoping to make some sense and maybe catch something. Any thoughts or ideas would greatly be appreciated. 
    • 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.
    • 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.
×
×
  • Create New...