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 Our Content
    eNewsletter
    Donate

I'm New With Blood Test Results And Qs


momof4inla

Recommended Posts

momof4inla Newbie

Hello, my name is Amy and I have been reading posts here on and off for about a week.

Last week I had a blood test, and yesterday I had a colonoscopy, ultrasound, and upper endoscopy. This morning I also had a CAT scan. All testing so far shows everything is normal. We are only waiting on biopsies.

My blood test results are as follows: (used Prometheus Labs)

AGA IgG: negative

AGA IgA: negative

TTG IgA: negative

EMA IgA: negative

Results do not support a diagnosis of celiac disease.

Assay Result:

AGA IgG: 2.2 reference range: <10.0

AGA IgA: <1.2 reference range: <5.0

TTG IgA: <1.2 reference range: <4.0

EMA IgA: negative

Total IgA: 182 reference range <3 years: 8-220

3-13 years: 41-395

>13 years to adult: 44-441

So my question is how likely is it that this is a false negative? I am waiting on biopsy results, however I don't think my doctor took more than one biopsy. He never did think I had celiac disease... in fact just by looking at me he said "Ah, not many people have that... your problem is IBS." <_< He gave me the celiac blood test to appease me.

He decided to run all the other tests to rule out everything else. Like I said, so far everything is normal.

I had decided to go to the Dr to begin with because I was tired of suffering and being sick all the time. A friend mentioned gluten and I dismissed it... this was several months ago. Then I had a really bad episode a couple of weeks ago, and while I was laying curled up in pain on my bathroom floor, I vowed to get to the bottom of this.

I remembered what my friend had said about gluten, and started reading on Celiac Disease and I became absolutely convinced that that is what is wrong with me. After all, 15 years ago (when I was 15 years old) I was tested for everything under the sun EXCEPT Celiac Disease. 15 years ago, I had no diagnosis. They just told me I had what "mimicked" IBS but that IBS sufferers usually don't vomit like I did.

Anyway... back to present day... my symptoms match what a Celiac suffers with...

Extreme bloating (look like I'm pregnant after eating)

Gas

Alternating Constipation/Diarrhea

Cramping and pain

Nausea

Sometimes extreme abdominal pain with or without vomiting

I also have:

acne

itchy skin

migraines and headaches

dry eyes

chronic fatigue

no energy

back pain

Mood swings

Irritability

I noticed that most of my pain comes after eating pasta dishes and anything with a gravy... I'm a South Louisiana girl and we like our rice and gravy! I never did eat much bread though...

I am also 100 pounds and 5'1", can't gain weight, and very small. (despite having s voracious appetite.) I have had stomach issues since childhood, with it becoming full force around the age of 15. As a newborn I was diagnosed as "failure to thrive" and didn't grow until my mother stopped breastfeeding and put me on soy formula. She also says I had a new skin rash every week. I also had allergies and asthma.

I just feel like I am 30 years old and tired of dealing with all this. I think I'm too young to feel this bad.

I am planning on starting a Gluten Free diet just to see if it helps. I couldn't believe that my blood test results were negative - I just could not believe it. I got a copy to see for myself. So just wondering if this could be falsely negative... and just hanging around waiting for biopsy results, although I don't have much faith in that either, since I'm pretty sure he didn't take enough samples.

So, my other question is - would just a gluten intolerance cause all those symptoms - without it being full-fledged Celiac?

Thanks for any help and time you can give me. I may be hanging around here more often for support in a gluten free diet!


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



Celiac.com Sponsor (A8-M):



tarnalberry Community Regular

Gluten intolerance could cause any of those symptoms, but there's no particular reason to assume that everything that doesn't feel right with you is from a gluten intolerance, even if you have one. So, while I encourage you to try a gluten free diet, don't give it up if only half of your symptoms resolve - that big of a change is still a very very telling sign

How likely a false negative? No one can tell you. Your plan - trying the diet - is the best way to go. Make sure to be quite careful about "hidden" gluten and cross contamination for the dietary trial to be worthwhile.

momof4inla Newbie

Thanks for replying, tarnalberry!

I don't mean to sound like i am assuming anything... I just really thought maybe it is that because I have been tested for everything else. I have even had my thyroid checked, and saw a cardiologist because of shortness of breath and other related symptoms. At that time they told me it was anxiety after all tests were normal, because I was sighing a lot. Sure enough... about 3 weeks after being told anxiety I had my first panic attack. Since then I also was diagnosed with hypoglycemia.

It's just that I never gave a food allergy or intolerance a second thought!

I don't want to accept that it's IBS and will just have to live with it. You know? I will gladly live with a certain diet if I could just feel better.

I was thinking about doing the Enterolab thing... it seems like that is more reliable, right?

I know that Celiac blood tests have a high instance of false negatives when a certain thing in the blood is insufficient (I can't remember at the moment) but I don't understand the test results so I don't know if mine was sufficient or not. :lol:

I don't want to do the Enterolab and spend more money if it's not likely that the test is wrong.

Everything is just so confusing. :blink:

How long should I try a gluten free diet if I expect to see changes? 3 weeks? 3 months? 6 months?

tarnalberry Community Regular

I don't think there's a really great rule for how long to try it. I'd vote three months.

The only reason I came across a little ... strident? something, anyway :P ... was that it can be easy to say "something is wrong with me", think we find an answer, and dismiss it when we don't get "all better". But it might not be gluten (or just gluten). If you notice that it's connected to when/what you eat, a food diary (or elimination diet, if you're up for that) may be worth while. Gluten, dairy, and soy seem to be the MOST common on here, but nightshades, uncooked fruits/vegetables, corn, eggs, nuts, and corn are also quite possible.

momof4inla Newbie

That is good advice, thank you. I guess I'll eliminate one "allergen" at a time? Or eliminate all and reintroduce one at a time?

Any other thoughts are welcome. :)

tarnalberry Community Regular

That is good advice, thank you. I guess I'll eliminate one "allergen" at a time? Or eliminate all and reintroduce one at a time?

Any other thoughts are welcome. :)

You can do an elimination diet either way - and if you search on here, you'll find posts from a lot of folks who have done them.

My background is in science, so my preference in doing an elimination diet is cutting out all but a dozen or so (literally) foods. Those foods you do eat should have a low potential for allergies and intolerances. You stick with that for a week or two, then add one food in for a week, and see if there's any change. Unfortunately, this is a horridly difficult way to go. While quite effective, I found it VERY hard to maintain, and stopped short (but I didn't have a lot of intolerances and didn't plan ahead well enough).

Doing it the other way is definitely doable, but it's harder to sort things out if you have multiple intolerances that way.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,171
    • Most Online (within 30 mins)
      7,748

    kyle68j
    Newest Member
    kyle68j
    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

    • DAR girl
      Looking for help sourcing gluten-free products that do not contain potato or corn derived ingredients. I have other autoimmune conditions (Psoriatic Arthritis and Sjogrens) so I’m looking for prepared foods as I have fatigue and cannot devote a lot of time to baking my own treats. 
    • Scott Adams
      I am so sorry you're going through this. It's completely understandable to feel frustrated, stressed, and disregarded after such a long and difficult health journey. It's exhausting to constantly advocate for yourself, especially when you're dealing with so many symptoms and positive diagnoses like SIBO, while still feeling unwell. The fact that you have been diligently following the diet without relief is a clear sign that something else is going on, and your doctors should be investigating other causes or complications, not dismissing your very real suffering. 
    • Oldturdle
      It is just so sad that health care in the United States has come to this.  Health insurance should be available to everyone, not just the healthy or the rich.  My heart goes out to you.  I would not hesitate to have the test and pay for it myself.  My big concern would be how you could keep the results truly private.  I am sure that ultimately, you could not.  A.I. is getting more and more pervasive, and all data is available somewhere.  I don't know if you could give a fake name, or pay for your test with cash.  I certainly would not disclose any positive results on a private insurance application.  As I understand it, for an official diagnosis, an MD needs to review your labs and make the call.  If you end up in the ER, or some other situation, just request a gluten free diet, and say it is because you feel better when you don't eat gluten.      Hang in there, though.  Medicare is not that far away for you, and it will remove a lot of stress from your health care concerns.  You will even be able to "come out of the closet" about being Celiac!
    • plumbago
      Yes, I've posted a few times about two companies: Request a Test and Ulta Labs. Also, pretty much we can all request any test we want (with the possible exception of the N protein Covid test and I'm sure a couple of others) with Lab Corp (or Pixel by Lab Corp) and Quest. I much prefer Lab Corp for their professionalism, ease of service and having it together administratively, at least in DC. And just so you know, Request a Test uses Lab Corp and Quest anyway, while Ulta Labs uses only Quest. Ulta Labs is cheaper than Request a Test, but I am tired of dealing with Quest, so I don't use them so much.
    • Scott Adams
      PS - I think you meant this site, but I don't believe it has been updated in years: http://glutenfreedrugs.com/ so it is best to use: You can search this site for prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
×
×
  • Create New...