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

Misdiagnosed?


Paintball Player

Recommended Posts

Paintball Player Newbie

Tl;dr I've never gotten Ill knowingly consuming products with gluten in it. I think I may have been misdiagnosed.

I'm starting to wonder if I've been misdiagnosed win celiac disease. I was diagnosed in late 2005 and since have maintained a rigid gluten free diet. Since then I've been fine and see the doctor biannually and my stomach/bloodwork is always perfect.

I've tried to see how bad I have allergic reactions to gluten products a few times since I was diagnosed.

#1 Test: I decided to have a slice of cheesecake on m birthday the year following when I was diagnosed. This was sort of a test sort of a birthday treat. I devoured the whole thing including the bread base of it.

Result: I was fine, felt great and nothing was wrong with my stomach.

#2 Test: I used regular flour bread instead of my gluten-free Bread a month ago. I felt fine and never got I'll.

#3 Test: I went to an army base for a course over the summer. I ate food on the base for all 7 days O was there; I know it was not gluten free. I never so much as felt a ping in my summer over the 21 non gluten free meals I consumed there.

It seems whenever I have an allergic reaction it's from something as minscule as a tiny amount of the wrong spice on a steak. I've never gotten sick when I have an indulgence and knowingly consume gluten products.

Furthermore; In my understanding celiac disease is a hereditary trait. Once I was diagnosed every single person in my family and extended family have had their bloodwork tested. Everybody is fine except for me. I am not adopted. The only thing similar to celiac disease is a lactose intolerance which a couple of my cousins (and maybe others) have.

So at this point I have become very skeptical about my 'diagnosis'. Does this sound like I may have been misdiagnosed?

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



psawyer Proficient

Celiac disease is NOT an allergy. It is, of course, possible to have celiac disease and also be allergic to wheat.

Your follow-ups being normal is normal when you are strictly following the gluten-free diet. Without gluten to provoke the autoimmune reaction, there are no gluten antibodies and your body heals so the villi are healthy.

It is possible to have "silent," or asymptomatic, celiac disease. It does not mean no harm is being done to your body when you ingest gluten.

You did not say how you were diagnosed. False negatives are possible with both the blood test and the biopsy, but false positives are extremely rare.

Link to comment
Share on other sites
ravenwoodglass Mentor

Celiac disease is NOT an allergy. It is, of course, possible to have celiac disease and also be allergic to wheat.

Your follow-ups being normal is normal when you are strictly following the gluten-free diet. Without gluten to provoke the autoimmune reaction, there are no gluten antibodies and your body heals so the villi are healthy.

It is possible to have "silent," or asymptomatic, celiac disease. It does not mean no harm is being done to your body when you ingest gluten.

You did not say how you were diagnosed. False negatives are possible with both the blood test and the biopsy, but false positives are extremely rare.

Agree strongly with this. In addition it used to be thought that young people would outgrow celiac because it can take some time for symptoms to appear after we have fully healed. Some will have organs other than the gut effected, issues with thought processes, mood, liver problems, thyroid, joint and muscle issues and so on before gut symptoms become apparent. If you were diagnosed by blood test or biopsy you need to stay gluten free for life.

As to the genetic aspect there are many who have the associated genes but don't develop the disease. Also some folks have impact to other organs but no gut symptoms and people in that instance have an even higher rate of false negatives on blood tests than those with gut issues.

Link to comment
Share on other sites
Lisa Mentor

How were you diagnosed? :)

There can be other causes for what would appear to be a positive biopsy.

From a Medscape article:

"Although villous atrophy is not exclusive of celiac disease, it is considered a crucial finding. Other causes of blunted villi include tropical sprue, malnutrition, intolerance to cow's milk, soy protein intolerance, and infectious gastroenteritis. However, most of these conditions can be readily excluded on the basis of clinical history and laboratory data."

Celiac Disease CAN and be a cumulative diagnosis through positive blood panel, biopsy/endoscopy exam and positive dietry results.

Link to comment
Share on other sites
Paintball Player Newbie

Thanks for the quick replies. Lisa, I had an endoscopy done at Vanderbilts Hospital (university hospital)

Link to comment
Share on other sites
Lisa Mentor

Thanks for the quick replies. Lisa, I had an endoscopy done at Vanderbilts Hospital (university hospital)

Well then, if you don't meet the criteria for the other issues that can cause intestinal atrophy, Celiac may be a true diagnosis.

As it's been mentioned many times, gluten sensitivity has a wide range. Having been gluten free for several years, it may take repeated and consistent gluten exposure for an unknown period of time, for you to achieve a reaction...perhaps by that time maybe some other issue may have jumped in your boat. <_<

I also do not react to cross contamination or even full exposure. I continue to be gluten free, but feel fortunate that I am not severely sensitive as many are here. :)

Link to comment
Share on other sites

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      121,213
    • Most Online (within 30 mins)
      7,748

    Chelsi
    Newest Member
    Chelsi
    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

    • Kirbyqueen
      Still dealing with this rash on my legs. I've eliminated ringworm (through use of topical ointments). And I also know it's not shingles, as I've never had chickenpox before and I'm still fairly young. Through a lot of online research, I'm leaning more towards dermatitis herpetiformis, eczema, or psoriasis. I've actually got a doctor's appointment in May (finally got some insurance) and I'm going to bring it up then. I'm feeling really hopeful and excited to maybe be getting some relief soon.   Big thanks to everyone for the suggestions and positive thoughts!
    • trents
      You have three celiac disease specific antibody tests that are positive: Endomysial  Antibody IGA (aka, EMA), tTG-IGA, and tTG_IGG. Furthermore, your Immunoglobulin A at 55 is low, meaning you are IGA deficient. This one is not an antibody test for celaic disease per se but a measure of "total IGA" levels and if low (yours is low) it can suppress the individual antibody scores and even cause false negatives. So, yes, it definitely looks like you have celiac disease.   Do not yet begin a gluten free diet as your physician may refer you to a GI doc for an endoscopy/biopsy of the small bowel lining for confirmation of the antibody testing. This may help:   
    • Bayb
      Hi, I received my labs via email yesterday and have not heard back from my doctor yet. Can anyone tell me if these results indicate I have Celiac?      Endomysial Antibody IgAPositive  Ft-Transglutaminase (tTG) IgA6  H0-3 (U/mL) - Negative 0 - 3 - Weak Positive 4 - 10 - Positive >10 - Tissue Transglutaminase (tTG) has been identified as the endomysial antigen. Studies have demonstrated that endomysial IgA antibodies have over 99% specificity for gluten-sensitive enteropathy. FImmunoglobulin A, Qn, Serum55  L87-352 (mg/dL) Ft-Transglutaminase (tTG) IgG183  H0-5 (U/mL) - Negative 0 - 5 - Weak Positive 6 - 9 - Positive >9
    • Aussienae
      Mine is definitely triggered by inflammation and stress! I do also have arthritis in my spine, but the pain is more in my pelvic area. Im sure i have other food intolerances or other autoimmune isues but the more I focus on it and see doctor after doctor, it just gets worse.  Best thing is get of Gluten! (I also avoid lactose). Try to limit stress and anything that causes inflammation in your body.
    • ButWhatCanIEat
      Good morning,   I got an email about replies to this post. Some of my doctors had blamed a slipped disc for the pain I had and that contributes, but after meeting with a gastroenterologist AGAIN and trying some lifestyle modifications, I found out I have IBS and can't tolerate corn or excessive fructose to any degree. Cutting out corn AFTER having cut out all gluten containing products was a real pain but I feel much better now!
×
×
  • Create New...