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

Blood Test Negative, But Could It Be Celiac?


kbenj1

Recommended Posts

kbenj1 Newbie

Hi, I am new to the gluten free diet. I tested negative for celiac in a blood test, but all of my symptoms disappeared once I went gluten free. Last night I ate a publix rotisserie chicken, and within an hour I hade aphthos ulcers on my throat, I was nauseous, my stomach was cramping, and I was gassy. My doctor thinks that the chicken was bad, but I think it was the gluten. It's been 24 hours, and I'm still not right. Could I have celiac?


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



Celiac.com Sponsor (A8-M):



Ninja Contributor

Hi kbenj1,

My diagnosis was tumultuous, just like many others' here. What I've learned (which may or may not be a popular opinion) is that it could always be Celiac. The tests are fallible - some have a 30% false neg. rate. Even with genetic testing, there's just so little known about the cause and necessary contributing factors that it's hard to make diagnosis fool-proof! It could be that the chicken was bad or it could be the gluten. Did anyone else have the chicken? Did they get sick?

I suggest that you request copies of all of the Celiac lab work. Many times doctors do not order the full Celiac panel, opting to just test TTG and total IgA. That would be the first thing to do. Does your family have a history of autoimmune diseases? Fertility issues? Vitamin deficiencies? All of the above? (:P)

Laura

Madagascar Rookie

if you've already gone gluten-free, getting tested again might not show if you do have gluten intolerance. Perhaps, as Laura said, you'll have more information if you see copies of your actual test results. my daughter (20) was tested last january and everything came back negative. we breathed a sigh of relief and celebrated. but her symptoms kept getting worse - she kept developing more food allergies, feeling worse, having more anxiety, and by november, i actually thought she was developing schizophrenia.

she went gluten & dairy free and within 4 days we were saying it was the gluten. it's now been a couple of months and she's a world better in every way. i got tested and mine came back positive, and i have the genes.

my point is that the tests aren't very reliable. what is reliable is if you go gluten-free for a 6 week trial and find that you are better. the reason people go gluten & dairy free is because the milk protein, casein, in some people's bodies, can 'look' like gluten and the body can react to it. i didn't go dairy free because i'm stubborn, i guess, but i'm doing fine.

rotisserie chicken does have gluten added to it by some stores. i don't know if all do, but i saw it listed on one i looked at. you could contact the store and see if anyone else reported getting ill. if no one else that ate it with you got sick as well, i'd think it was not food poisoning.

kbenj1 Newbie

Thanks so much for your replies. My husband and daughter ate the chicken and were fine. The one I ate was the barbecue flavor, and it definitely has gluten. There are autoimmune issues in my family-my mother has 7 different ones, and I'm wondering if she has celiac but doesn't know it. My daughter has stomach problems and eczema, and I'm wondering if she might have an allergy as well. The tests I had done were the IgG IgA. Are there others tests I should do? I know having gone gluten free will alter any biopsies I may need, but I am desperate for relief!

mushroom Proficient

You may or may not have celiac, but it does sound like you might be gluten intolerant. There are several other tests which make up the celiac panel, which consists of the following:

Anti-Gliadin (AGA) IgA

Anti-Gliadin (AGA) IgG

Anti-Endomysial (EMA) IgA

Anti-Tissue Transglutaminase (tTG) IgA

Deamidated Gliadin Peptide (DGP) IgA and IgG

Total Serum IgA

As you can see, none of them is labelled IgG IgA (maybe it was AGA IgA?) They normally run the IgA versions of tests unless total serum IgA is insufficient. My personal opinion is that the DGP is the most likely to give an accurate result, although if any of the tests is positive it should be explored further. I don't know how long you have been eating gluten free? If longer than two weeks you would need to resume eating gluten for a while.

kbenj1 Newbie

My blood work only lists IgG and IgA. It doesn't break those tests down the way you did. I will ask my doctor about it. I have been gluten free for 16 days now, and have felt better than I have in years. But my symptoms have started to recur after eating the publix chicken(see above post). Not sure if it is gluten or something else. It's been over 48 hours and I'm still not feeling well. Had an ultra sound of my abdomen today to rule out other problems. I see my dr next week, so hopefully I will get some answers.

Madagascar Rookie

the only part of my tests that came back definitive was the TTG - Tissue Transglutanimase IGA. Labs measure things differently, but I had mine sent to Prometheus Labs and the local lab accidentally sent it to their usual PeaceHealth Labs. So i ended up with results from 2 different labs, interpreted differently, from the exact same blood sample.

The tests these 2 labs ran were

Immunoglobulin A (IgA)

Endomysial Antibody, IgA

Gliadin IgG

Gliadin IgA

Tissue Transglutaminase IGA

The celiac specialist my family is working with said that a study was done where blood samples from people with known celiac disease were sent to various labs and there was only a 30% accuracy rate in the results. Meaning that they missed 2/3 of the diagnoses.

The fact sheets on this page from the University of Chicago's Celiac Center are full of great information: Open Original Shared Link

and this e-book (lower right corner of page) is equally helpful: Open Original Shared Link

Celiac disease is genetic. When my daughter went gluten-free, I spent the next 3 days researching online and by the time i was done i knew without a doubt that I also had it, my brother and mother as well. I opened a facebook conversation with 8 of my cousins on my mom's side to ask them about health problems - and the answers just confirmed for me that was the genetic link. Getting the test was just a formality.

There's really no advantage to having a diagnosis in the US, unless you want one. If you thrive being gluten-free and are sick when you eat it, that's really all you need to know. i did get the genetic test, which Prometheus Labs will do. However, while I have the gene, by its location the Prometheus Labs report says that i have a low chance of having celiac - 2 out of their scale of 8. And yet, I have it. the Celiac Specialist here said that if you have the gene, you have it.

What you're describing with your mom and your daughter sounds like you're all in the same boat.


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



Celiac.com Sponsor (A8-M):



kbenj1 Newbie

Thank you so much for the information!

Madagascar Rookie

good luck!

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. - Colleen H replied to Colleen H's topic in Gluten-Free Foods, Products, Shopping & Medications
      15

      Ibuprofen

    2. - Colleen H posted a topic in Coping with Celiac Disease
      0

      Methylprednisone treatment for inflammation?

    3. - cristiana replied to Colleen H's topic in Gluten-Free Foods, Products, Shopping & Medications
      15

      Ibuprofen

    4. - Jmartes71 posted a topic in Coping with Celiac Disease
      0

      My only proof

    5. - Scott Adams replied to wellthatsfun's topic in Coping with Celiac Disease
      1

      still struggling with cravings


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,871
    • Most Online (within 30 mins)
      7,748

    GR82BNTX
    Newest Member
    GR82BNTX
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Colleen H
      Yes thyroid was tested.. negative  Iron ...I'm. Not sure ... Would that fall under red blood count?  If so I was ok  Thank you for the detailed response..☺️
    • Colleen H
      Hi all !! Did anyone ever get prescribed methylprednisone steroids for inflammation of stomach and intestines?  Did it work ??  Thank you !! 
    • cristiana
      Hi Colleen Are you supplementing B12/having injections? I have learned recently that sometimes when you start addressing a B12 deficiency, it can temporarily make your symptoms worse.  But it is important not to stop the treatment.  Regarding your problems with anxiety, again that is another symptom of a B12 deficiency.   I didn't know what anxiety was until it hit me like a train several months before gastrointestinal issues began, so I can certainly relate.   Two books which helped me hugely were At Last A Life by Paul David (there is a website you can look up) and The Depression Cure: The Six-Step Programme to Beat Depression Without Drugs by Dr Steve Llardi.  Although his book is aimed at people who have depression, following the principals he sets out was so helpful in lessening my anxiety.  Llardi suggests we need to focus on getting enough: - physical exercise - omega-3 fatty acids - natural sunlight exposure - restorative sleep - social connectedness - meaningful, engaging activity   ... and we should feel a lot better. That is not to stay you must stop taking medication for depression or anxiety if you have been prescribed it, but adopting the changes Dr Llardi sets out in the book should really help. Can I just ask two more questions:  1) you say that you are B12 deficient, did they test your iron levels too?  If not, you really ought to be checked for deficiency and, 2) did they check your thyroid function, as an overactive thyroid can be cause rapid heartbeat and a lot of coeliacs have thyroid issues? Cristiana        
    • Jmartes71
      Hello still dancing around my celiac disease and not getting medically backed up considering Ive been glutenfree since 1994.All my ailments are the core issue of my ghost disease aka celiac disease. Im angery because the "celiac specialist " basically lightly dismissed me.Im extremely angery and fighting for a new primary care physician which is hard to do in Northern Cali.So currently without and looking.Im angery that its lightly taken when its extremely serious to the one who has it.My only evidence is a brochure back in the days when I got news letters when I lived at my parents.It was published in 1998.I was diagnosed before any foods eliminated from my diet. Angery doctors don't take seriously when Im clearly speaking.I did write to the medicine of congress and have case number.
    • Scott Adams
      I totally get this. It's absolutely a grieving process, and it's okay to feel gutted about the loss of those simple joys, especially at 18. Your feelings are completely valid—it's not about being ungrateful for your amazing boyfriend, it's about mourning the life you thought you'd have. That "tortured by the smell" feeling is so real. It does get easier, I promise, but it's okay to sit in the sadness and just vent about how much it stings right now. Thanks for sharing that. Celiac.com has published a book on our site by Jean Duane PhD called Gluten-Centric Culture, which covers many of the social aspects of having celiac disease: This chapter in particular covers issues around eating with family and others - Gluten-Centric Culture: Chapter 5 - Grabbing A Bite Together:    
×
×
  • 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.