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

About To Get The Results Of My Celiac Panel


micaela27

Recommended Posts

micaela27 Newbie

i have gastroparesis (delayed stomach emptying that is usually associated with diabetes, which i DON'T have) and an autoimmune condition called Hashimoto's Thyroiditis that have both been recently diagnosed. given the autoimmune nature of my thyroid problems, i got tested for celiac disease last week and am awaiting the results tonight at my GI appt. based on my research, i learned that both gastroparesis and my thyroid condition are associated with celiac disease so i'm almost expecting a diagnosis tonight.... but what if my GI doctor says everything looks clear? i don't have any classic symptoms of gluten intolerance, though i have lots of problems related to my delayed stomach emptying from the gastroparesis... but i don't have excess gas, bloating, diarrhea, etc. still, i have heard from multiple sources that the blood test isn't always completely accurate in pinpointing gluten intolerance. so... should i go gluten-free anyway if i get a negative test result? i read about so many people who had the problems, tested negative, and went gluten-free anyway with fabulous and immediate results. i just want my gastroparesis to go away and the fact that it came out of NOWHERE in a perfectly healthy individual with a spotless medical record and impeccable eating habits (i'm a nutritionist) leads me to believe something else is causing my problems. i'm almost hoping for a celiac diagnosis... because that would give me a glimmer of hope that maybe i could do something definitive to correct my stomach issues. does anyone else have gastroparesis or Hashi's?? whaddya think? thanks!


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



Celiac.com Sponsor (A8-M):



Nantzie Collaborator

I always think that people who suspect gluten issues should try the gluten-free diet despite test results. There are just too many of us who tested negative but had life-changing results. It's worth it just to give it a try.

There seem to be patterns among those of us with negative tests, based on related "gluten intolerance" genes, that have certain symptom profiles.

With the gene that I have, you're looking at GI and neuro symptoms, but negative medical tests. I also seem to see a pattern of hypersensitivity to gluten.

If you respond well to the gluten-free diet, it will be a great experience. Because if you're reacting to gluten, it's probably effecting other areas of your life that you may not be aware of. Personally, things like anxiety, headaches, balance problems, fibromyalgia-type pain, insomnia all went away.

If you don't respond to the gluten-free diet, you'll at least know this isn't the answer for you. There are a lot of people here with other food intolerances that can help you try eliminating other foods that cause problems, like soy, dairy, corn, eggs, etc.

Welcome to the board. Let us know how your tests turn out.

Nancy

kbtoyssni Contributor

I am a firm believer in the fact that if you have something going on in your digestive tract, you should look at what you're putting in it first. Blood tests give false negatives fairly often so why not try gluten-free just in case? It's easy to do and can save you a lifetime of suffering if you do have celiac. It's not like you'll harm your body by trying gluten-free. The catch is that you have to do it 100% to really know for sure. You have to be diligent about cross contamination and ingesting small amounts of gluten because that can be enough to make you not feel better if you do have celiac. Good luck and welcome!

micaela27 Newbie

well my celiac panel came up negative for antibodies and as it turns out, during my endoscopy last month my GI doctor did a biopsy and it was also negative. should i still be concerned? i have no symptoms, just the gastroparesis and the autoimmune thyroid problem. my doctor said he was 99% sure i did not have celiac disease based on the double negative test results. so where does that leave me?

test results on paper state:

(tTG) AB, IGA <3 (ref range <5 is negative, 5-8 is equivocal, >8 is positive)

endomysial AB IGA (test not performed. reflex testing not required.)

endomysial AB titer (test not performed. reflex testing not required.)

Gliadin AB IGA <3 (ref range <11 is negative, 11-17 is equivocal, >17 is positive)

IGA Serum 613 (ref range 81-463 mg/dL) OUT OF RANGE

(tTG) AB, IGG (not performed.)

what does it mean that my IGA Serum is high?

Nantzie Collaborator

I'm not sure very well versed on the IgA. Maybe one of our more science-y members will see this and can help.

Since you are under the care of a doctor, and you've already been tested for all sorts of things I'm sure, I'd say you should try the diet (100%) for a few months and see what happens.

It's only classic celiac that will show up in blood tests and biopsies. You may have non-celiac gluten intolerance, like so many of us here do.

Another question I had, because you mentioned you are a nutritionist, is do you eat a lot of soy? Even though it's considered healthy, soy can really mess people up, so that would be something I would suggest looking into as well.

I hope you start feeling better soon.

Nancy

micaela27 Newbie
Another question I had, because you mentioned you are a nutritionist, is do you eat a lot of soy? Even though it's considered healthy, soy can really mess people up, so that would be something I would suggest looking into as well.

good question! i used to drink soy milk and upon reading that it can have negative effects on the thyroid, i stopped and went to skim milk about 2 or 3 weeks ago. so... no, i really don't do soy products anymore. all my dairy foods are actual dairy and not soy versions. i don't eat tofu, i haven't had my soy protein shake in months at this point. i do eat edamame on occasion, but again... not in awhile. it's been at least a month. i am going to follow up with my GI tomorrow regarding this IGA serum business... i was speaking with a friend who is currently in med school and she was explaining that the IGA serum levels being elevated indicates i am acutely sick with something. the fact that i have a diagnosed autoimmune disease could be the cause of it, but it also could be an indicator of something else. anyway... i plan on getting to the bottom of this tomorrow. thanks for the advice so far! i'll post an update tomorrow if i find anything of value to include.

nora-n Rookie

If you go to Dr. Ford's webpages, he explains about the antigliadin IgG test. You might want to ask for that one.

The other tests probably will not get positive until the villi have disappeared....the antigliadin IgG probably rises much faster and may show celiac or gluten-intolerance a long time before the villi are gone.

Open Original Shared Link

And, have you read at the blog at thefooddoc.com ?

nora


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



Celiac.com Sponsor (A8-M):



Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,565
    • Most Online (within 30 mins)
      7,748

    Gma Marsh
    Newest Member
    Gma Marsh
    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.