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

Negative Results


lemonade

Recommended Posts

lemonade Enthusiast

I have had a blood test and a biopsy which both came back negative for celiac disease. How every the gasto doctor said that I am gluten intolerant and that if i were to stay on gluten i may have celiac disease. Is it possible to be diagnosed with celiac disease if both tests come back negative?

has anyone here been in the same position as me?

I will also be tested by enterolab, so well see what my results will be. Is it possible to have a negative biopsy and blood test but positive result for celiac disease with enterolab?

thnx

L


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



Celiac.com Sponsor (A8-M):



penguin Community Regular

It is possible. Blood tests aren't that sensitive, especially if you weren't eating gluten before the test. And with the biopsy, the small intestine is 22 ft. long and the endoscope only sees 5 ft of that. It also depends on your dr, how many samples he took, and how the lab interpreted it.

Even if you're only gluten intolerant, the treatment is the same. Gluten free diet for life.

(((hugs)))

Good luck! :)

Rachel--24 Collaborator

Enterolab cant diagnose Celiac Disease but the results will definately tell you if you're gluten intolerant. Did you order the gene test? If you end up having a Celiac gene you could assume continuing to consume gluten will eventually lead you to Celiac.

lemonade Enthusiast

Thanks for the replies,

I ordered the compete test package from enterolab

L

Guest nini

my opinion is that POSITIVE DIETARY RESPONSE is THE MOST VALID diagnostic tool there is. The blood tests and biopsies can only confirm it. They CANNOT ever say that they are completely negative. There are too many unknown factors still. Too many people that have gluten intolerance or have developed full blown Celiac after having negative tests and being told they could continue eating gluten.

Ultimately, your body is the best tool. Listen to it. If your body tells you it feels better off of gluten, even if it's not 100% better, listen. I had a positive blood test, but chose not to have the biopsy. My blood test results were HIGHLY conclusive along with my symptoms and my incredible positive dietary response. I've been gluten-free for 3 years now (end of March) and while I am mostly better, since I went undiagnosed for 33 years, I still have many health issues I'm dealing with. But I can tell without any doubts that my body reacts VIOLENTLY to gluten. And this is without a so called gold standard biopsy. Again, I repeat, Positive Dietary Response is your most valid diagnostic tool, listen to your body!

lemonade Enthusiast

thanks for the reply!

yunalesca Newbie

Hi Lemonade, sorry you didn't get the results you were hoping for - I know how disappointing that is. It might be a good idea to get the blood tests rechecked at a later stage if you don't find out anything definite. I had been tested (blood test) in early 2004 (although I didn't know until later) & it came back normal, and later in 2005 I had 2/3 levels positive. I'm still without diagnosis but I'm going to try a gluten-free diet and hope I feel better. Hope the enterolab is more helpful :)


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



Celiac.com Sponsor (A8-M):



tiredofdoctors Enthusiast

Here's the skinny on the "Gluten Intolerance": A. You can be gluten intolerant without having Celiac Disease B. You can't have Celiac Disease without being gluten intolerant

It's kind of those set/subset things!

teankerbell Apprentice

Yes my blood test was negative. Stool test was positive for gluten sensitivity, the celiac gene and casein.

My doctor says that the blood test and biopsy are not always reliable, no test is. He feels if you feel better getting off gluten, then you have your answer.

Good luck.

CMCM Rising Star

I agree with the others. My blood test came back negative. But thru Enterolab I got very positive results and learned I have two genes, one for celiac and one for gluten. Either way (i.e. with gluten OR celiac genes) the "cure" is the same: don't eat gluten. They can both make you sick. And ultimately, Nini is right....the answer is in the diet. If eating gluten makes you sick, why continue with it?????? The answer is actually quite simple! And the positive thing is, NO DRUGS are necessary to "cure" you!!

Enterolab also told me I was casein sensitive, and on my own observation I think I'm also lactose intolerant. But because of the casein test results, Dr. Fine said I should not have dairy either, and that continuing to eat casein I could also damage my intestines in the same exact way that eating gluten does. So the message is clear: It's all in the diet, and you need to take any sensitivity seriously.

By the way, as one book I'm reading states: If you stop eating gluten, your intestines heal and you no longer have celiac disease....you just have the predisposition to it if you added back the trigger, which is gluten. Remember that celiac disease is actually the term given to the observed intestinal damage seen via a biopsy. Gluten sensitivity is a huge spectrum of reactions, ranging from none at one end to celiac disease at the other end. And all celiac disease starts as gluten sensitivity, although apparently not all gluten sensitivity will lead to celiac disease (the damage). But BOTH can create the same unpleasant symptoms, which is why for both the prescription is identical: don't eat gluten!!

Another interesting factoid: Celiac disease is the ONLY autoimmune disease in which the environmental trigger (gluten) is identified and known! So other autoimmune diseases most likely also have some sort of specific trigger...scientists just haven't yet figured out what the trigger is. The other thing to remember, however, is that when you have one autoimmune disease actively occurring...such as celiac disease....you open the door to others, such as rheumatoid arthritis, lupus, etc. This is why it's so important to get a handle on this and stop eating gluten!!!

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - wellthatsfun posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      0

      nothing has changed

    2. - trents replied to Charlie1946's topic in Related Issues & Disorders
      48

      Severe severe mouth pain

    3. - Charlie1946 replied to Charlie1946's topic in Related Issues & Disorders
      48

      Severe severe mouth pain

    4. - Charlie1946 replied to Charlie1946's topic in Related Issues & Disorders
      48

      Severe severe mouth pain

    5. - Jmartes71 replied to Jmartes71's topic in Related Issues & Disorders
      3

      New issue

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,102
    • Most Online (within 30 mins)
      7,748

    Dawn74
    Newest Member
    Dawn74
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • wellthatsfun
      i have been strictly gluten free for 7 months. this includes avoiding anything that may contain gluten and making sure surfaces and appliances are clean. i am 18 years old in australia and my tTG-IgA results were 69U/mL, pretty low compared to most people's, for reference. i feel the exact same as before. sure, i was pretty much asymptomatic/silent. the worst i'd get was occasionally bad stools and pitting of the nails/brittle hair since early childhood - and i was diagnosed with low iron and vitamin d which checks out due to easy bruising and such. but those symptoms have remained. maybe i'm jumping the gun, sure. i know it can take years to fully heal. but being over half a year in, i feel that i should be, y'know, healing. i'm nearly at my wits end and wondering if i should have a piece of bread or something to see how i go - to see if i possibly have refractory? my mental health is declining as i feel myself wanting to bang my head against a damn wall out of frustration every day. cravings haven't gotten better. look, i love the stuff i still can have, like salads and such. OH! i haven't lost any weight, which is mind boggling considering i eat very healthily now! i've always been on the chubbier side which is atypical of coeliac. i just don't know what's going on with me. i try to remain hopeful but i'm just so sad all the time. thanks for reading  
    • trents
      @Charlie1946There is a PM (Personal Message) tool built into the forum website that allows you to send a private message to other forum users. Just hover over their name with your mouse cursor and the menu containing that tool will pop up. This is useful if you want to communicate with an individual without everyone else involved in the thread seeing it.  Are you realizing that in my PPI taper down recommendations in an earlier post above, I was responding not to your posts but to @Caligirl57? If you must use a PPI, I certainly would advise taking the lowest dose that is effective for you.  
    • Charlie1946
      Hi everyone, I'm still trying to figure out how to each message individually. I saw one with some information on sebaceous hyperplasia but now I can't find it. I appreciate you all so much for all your responses and advice! God bless! Hi everyone, I'm still trying to figure out how to each message individually. I saw one with some information on sebaceous hyperplasia but now I can't find it. I appreciate you all so much for all your responses and advice! God bless! Hi everyone, I'm still trying to figure out how to each message individually. I saw one with some information on sebaceous hyperplasia but now I can't find it. I appreciate you all so much for all your responses and advice! God bless! Hi everyone, I'm still trying to figure out how to each message individually. I saw one with some information on sebaceous hyperplasia but now I can't find it. I appreciate you all so much for all your responses and advice! God bless! Hi everyone, I'm still trying to figure out how to each message individually. I saw one with some information on sebaceous hyperplasia but now I can't find it. I appreciate you all so much for all your responses and advice! God bless!
    • Charlie1946
      @trents thank you! I have only been taking 20mg 1x a day. Maybe I need to increase it.
    • Jmartes71
      Nope its just me because they can eat wheat and when we use same pans I found out last year thanks to you guys and the autoimmune website im learning,we are not to share though clean, same with sponge. I just wish doctors understood. I am with new gi and new pcp but im falling apart because blood work is fabulous.Im so ANGERY.I have reached out to my local representative, in Stanislaus but its just weekly stuff.Im going to need to physical go down there.Any recommendations on what to say and do because this is absolutely ridiculous. If I didn't have my husband though we are really hurting with one income, I would absolutely be one of the homeless population. Thats alarming begging to be heard about a diagnosis that was given as an adult and dealing with this, medical needs to stick to patients regardless of switching insurance or doctor. 
×
×
  • 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.