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

Unclear Diagnosis


edie

Recommended Posts

edie Newbie

I am 43 year old mother,runner, active athletic woman that has been plagued with stomach issues since having my gallbladder out, a bout with horrible stomach flu and mono that landed me in the hosptial last year. I have had abdominal pain, constant fullness and bloating, bowel issues with terrible pain for the last 3 years. I have been prescribed the usual nexium, zantact, Levsin and antibiotics with no relief. My initial endoscopy 3 yrs ago was negative for celiac ( several months after symtpms started) but I had many many areas of micro erosions in my stomach into my small intestines. Tiny infammation areas they thought were related to Ibuprophen.

The latest is a diagnosis of IBS...of course.

3 year later, still symptomatic, colonoscopy results normal, blood test normal ( neg. for celiac) , scheduled for endoscopy in 2 days as my new doctor said many people test negative on blood for celiac and positive on biospy. She says I "look celiac"...whatever that mean. I am very thin, trouble keeping weight on and am NEVER hungry.

Is it possible to be celiac and have so many negative tests? Is it worth trying gluten free....I have tried everything else. My entire family has autoimmune disease ( thyroid, diabetes type I, vitiligo, etc ).


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



Celiac.com Sponsor (A8-M):



gfb1 Rookie
I am 43 year old mother,runner, active athletic woman that has been plagued with stomach issues since having my gallbladder out, a bout with horrible stomach flu and mono that landed me in the hosptial last year. I have had abdominal pain, constant fullness and bloating, bowel issues with terrible pain for the last 3 years. I have been prescribed the usual nexium, zantact, Levsin and antibiotics with no relief. My initial endoscopy 3 yrs ago was negative for celiac ( several months after symtpms started) but I had many many areas of micro erosions in my stomach into my small intestines. Tiny infammation areas they thought were related to Ibuprophen.

The latest is a diagnosis of IBS...of course.

3 year later, still symptomatic, colonoscopy results normal, blood test normal ( neg. for celiac) , scheduled for endoscopy in 2 days as my new doctor said many people test negative on blood for celiac and positive on biospy. She says I "look celiac"...whatever that mean. I am very thin, trouble keeping weight on and am NEVER hungry.

Is it possible to be celiac and have so many negative tests? Is it worth trying gluten free....I have tried everything else. My entire family has autoimmune disease ( thyroid, diabetes type I, vitiligo, etc ).

trying a gluten-free diet costs nothing.

it is absolutely possible to have negative tests and still be a celiac. this is (mostly) due to the high variability in the age of onset and response/severity to gluten at that time. i strongly suspect that in many people much of the celiac symptomology occurs long before there is sufficient and consistent intestinal damage to provide a positive blood test. your body responds much more quickly (and locally) than the mechanisms tested for in the blood.

however... sometimes a negative is really a negative (or a cigar...).

lizard00 Enthusiast
trying a gluten-free diet costs nothing.

it is absolutely possible to have negative tests and still be a celiac. this is (mostly) due to the high variability in the age of onset and response/severity to gluten at that time. i strongly suspect that in many people much of the celiac symptomology occurs long before there is sufficient and consistent intestinal damage to provide a positive blood test. your body responds much more quickly (and locally) than the mechanisms tested for in the blood.

however... sometimes a negative is really a negative (or a cigar...).

I believe that, too. I think that is why the average time it takes to be diagnosed is around 11 years, simply because our bodies are telling us something is wrong loooong before it can actually be detected through the testing available. I believe this was my case, only 2 years of damage, combined with a low IgA, pretty much made it impossible to detect through testing.

My doctor does treat me as a celiac patient, and we both believe I have celiac.

Once you get your EGD, give the diet a try. You have nothing to lose, it's not an unhealthy diet, and if it works, you can control how you feel by diet, and don't have to be reliant on drugs.

Wish you the best!

edie Newbie

I believe that my wonderful gastroenterologist feels this is Celiac as she is repeating everything I had done 3 years ago and after my colonoscopy she DID recommend I try a Gluten Free diet after the small intestine biopsy Friday. She says with my family hx, symptoms, sudden onset , and apparently the way I look she feels it is worth a shot. So, I guess I will give a try starting Saturday. I just find it hard to believe that I all of a sudden have developed IBS. But, then again I think that most of the biopsies and blood test are highly sensitive...very confusing! Thanks.

lizard00 Enthusiast

Welcome to the forum, by the way! :)

Getting started with the diet can be tricky, so feel free to ask away!!

mommida Enthusiast

Many people here are self diagnosed after negative test results. I would try the diet no matter what the test results are.

If you are suffering from one or more food intloerances, a food journal can really help you figure out what's going on.

Welcome to the board!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,561
    • Most Online (within 30 mins)
      7,748

    lamps
    Newest Member
    lamps
    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

    • petitojou
      Thank you so much for sharing your experience and I found myself giggling with happiness as I read how your body reached such spring! And I hope that your current journey is also successful!! Definitely starting the food diary! So many amazing advices. And it’s very scary. It really hits all our soft spots as well as our confidence system. Most doctors I went thought I was underage despite being in my late 20s. Right now I look like am I twelve, but is also this body that’s taking so much, so I might as well love it too! Going to make the necessary changes and stay in this path. Thank you again! 🫶
    • petitojou
      Thank you so much for the information and kind message! Reading this transformed how I’ve been viewing my efforts and progress. Guess there’s still a lot to celebrate and also heal 😌  Yes, I’ve been taking it! Just recently started taking a multivitamin supplement and separated vitamin D! I also took chewable Iron polymaltose for ferritin deficiency 2 months ago but was unable to absorb any of it.  Thank you again! Hearing such gentle words from the community makes my body and heart more patient and excited for the future. 
    • ckeyser88
      I am looking for a roomie in Chicago, Denver or Nashville! 
    • Scott Adams
      Your post demonstrates the profound frustration and isolation that so many in the Celiac community feel, and I want to thank you for channeling that experience into advocacy. The medical gaslighting you endured for decades is an unacceptable and, sadly, a common story, and the fact that you now have to "school" your own GI specialist speaks volumes about the critical lack of consistent and updated education. Your idea to make Celiac Disease a reportable condition to public health authorities is a compelling and strategic one. This single action would force the system to formally acknowledge the prevalence and seriousness of the disease, creating a concrete dataset that could drive better research funding, shape medical school curricula, and validate the patient experience in a way that individual stories alone often cannot. It is an uphill battle, but contacting representatives, as you have done with Adam Gray, is exactly how change begins. By framing it as a public health necessity—a matter of patient safety and protection from misdiagnosis and neglect—you are building a powerful case. Your voice and your perseverance, forged through thirty years of struggle, are exactly what this community needs to ensure that no one else has to fight so hard just to be believed and properly cared for.
    • Scott Adams
      I had no idea there is a "Louisville" in Colorado!😉 I thought it was a typo because I always think of the Kentucky city--but good luck!
×
×
  • 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.