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

I Need Verification If Correctly Tested For celiac disease


nb-canada

Recommended Posts

nb-canada Apprentice

It has been a year since my 35 year old son was positively diagnosed with celiac disease - blood test, biopsy & DH was positive. I unfortunately had negative tests. I have been gluten-free for 7 months & feel great except for fatique & the occassional episode of accidental glutening. In my opinion, I have had celiac disease most of my life.

My question - did I get the proper blood testing? My family doctor says it was the best test and that it was sent to a lab in Toronto. I have a copy of the results and they were from another hospital in my province - therefore I don't have much faith in the results. :(

The test results are -

- Immunoglobulin IgG 6.84 (4.54 - 14.99 g/L)

- Immunoglobulin IgA 1.23 (0.32 - 3.40 g/L)

- Immunoglobulin IgM 3.83 (0.15 - 2.27 g/L)

As you can see the only test not normal is the IgM. But as far as I am concerned these tests are not the best tests for celiac disease. What do you think?

Also ony 3 samples from my endoscopy were biopsied. Results - small intestinal mucosa with mild lymphocytic infiltration; no pathological changes of celiac disease is identified.

I don't have a lot of faith in the GI either because his first comments to me were - "you are too fat to have celiac disease" and "you are too old". I should have walked out then because I think the whole thing was a waste of time. We have to educate these doctors!

Thanks in advance for your opinions! :D


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



Celiac.com Sponsor (A8-M):



Gerri Explorer
It has been a year since my 35 year old son was positively diagnosed with celiac disease - blood test, biopsy & DH was positive. I unfortunately had negative tests. I have been gluten-free for 7 months & feel great except for fatique & the occassional episode of accidental glutening. In my opinion, I have had celiac disease most of my life.

My question - did I get the proper blood testing? My family doctor says it was the best test and that it was sent to a lab in Toronto. I have a copy of the results and they were from another hospital in my province - therefore I don't have much faith in the results. :(

The test results are -

- Immunoglobulin IgG 6.84 (4.54 - 14.99 g/L)

- Immunoglobulin IgA 1.23 (0.32 - 3.40 g/L)

- Immunoglobulin IgM 3.83 (0.15 - 2.27 g/L)

As you can see the only test not normal is the IgM. But as far as I am concerned these tests are not the best tests for celiac disease. What do you think?

Also ony 3 samples from my endoscopy were biopsied. Results - small intestinal mucosa with mild lymphocytic infiltration; no pathological changes of celiac disease is identified.

I don't have a lot of faith in the GI either because his first comments to me were - "you are too fat to have celiac disease" and "you are too old". I should have walked out then because I think the whole thing was a waste of time. We have to educate these doctors!

Thanks in advance for your opinions! :D

I didn't get to see my results. I was told to go on a gluten free diet indefinitely. Three weeks later and after some blood was done, I seen my GASTRO, she said that there was possible chance I was Celiac, as my blood work showed a great improvement. After having an endoscopy (no results yet). Gastro said I might only be gluten intolerant and what I have read that many gluten intolerant change to celiac. Blood test and endoscopy don't always confirm celiac.

I already had a doctor tell me that he would have diagnosed me with Celiac, without the endoscopy. As he was at Urgent care clinic and not family doctor, I don't know if that counts. Celiac you can gain weight, be constipated all the time. It is also know fact that biopies only taken from very small section on small intestine, and very frequently not taken from the damage area. Corn, gluten cause celiac problems different parts of the small intestine. I have major problems with corn, and products made with corn, as well.

If you feel better following a gluten free diet, you have your answer. I could not handle one more day of eating gluten, corn, and have really restricted my diet from these things, and feel much better. I believe I have been Celiac, and had signs since I was a toddler, and now 54. No one can pay me to go back on gluten or corn, no way no how.

I see you live in Canada (NB), I am in ON.

Hugs

Gerri

cat3883 Explorer

It looks like you werent tested for TTG whatever that is. The other bloodwork that you you had came back normal for me. The TTG for me was at 59 with the normal range of 0-19. Anything over 30 shows strong positive. My GI then did the genetic test and I came back positive for both genes. My biopsy is this Wednesday. I cannot go gluten free until then and I cant wait. The doc knows I have celiac even before the biopsy. He is doing it just to see where I am at before I begin my new lifestyle. I am so fortunate to have the right Doc. Good luck to you.

Nancym Enthusiast

Blood tests are negative sometimes when there isn't total villious atrophy. Also, blood tests don't tell you anything about gluten sensitivity without villious atrophy. For that, you'd need a test like Enterolab.com does.

nora-n Rookie

Those are not celiac tests.

But, when testing for celiac, (ttg IgA ans antigliadin IgA and endomysium abs), they also run the total IgA just to check if the tests I listed are valid. In case of selesctive IgA deficiency (about 10% of the population have that) they ahve to run the IgG versions of those tests.

Again, they did not run any celaic tests on you. Shame on them. go back and inform them they did not run any celiac tests on you, just the rutine IgA test to see if the celiac tests that were not done, are valid.....I hope they do not do this stupid testing on all patients they think they are testing for celiac.

About the lymphocytic infiltration:

Some places will diagnose you with celiac with increased intraepitelial lymphocytes together with symptoms etc. Go find Dr. Lewey's website, there he explains how many of them are normal per villi tip and how many are abnormal. I have read in Don Wiss's postings on some other forums that some places will diagnose you toghether with some other info that points to celiac if you ask for a second opinion on the slide. I think it was the U of Maryland. Dr. Lewey is at www.thefooddoc.com

nora

  • 4 months later...
nb-canada Apprentice
About the lymphocytic infiltration:

Some places will diagnose you with celiac with increased intraepitelial lymphocytes together with symptoms etc. Go find Dr. Lewey's website, there he explains how many of them are normal per villi tip and how many are abnormal. I have read in Don Wiss's postings on some other forums that some places will diagnose you toghether with some other info that points to celiac if you ask for a second opinion on the slide. I think it was the U of Maryland. Dr. Lewey is at www.thefooddoc.com

nora

Thanks Nora. I just seen your post today and I really appreciate your response. I checked out Dr. Lewey's site. Very interesting. I think I may print out the info and show it to my doctor. It does seem that my biopsy results could mean celiac especially with the results of a gluten free diet and my son's definite diagnosis. My family doctor has given me a diagnosis of Gluten Intolerant but it would be nice to have the Celiac diagnosis so I could claim the expenses on my Income Tax. Do you know how long a slide is kept in the lab? It would be nice to get a second opinion.

I have been diagnosed with Hypo Thyroid and had Shinges (for 5th time) since this post. Besides that I am feeling great....still gluten free :).

tarnalberry Community Regular

(EDIT: doesn't apply to this thread, as the below is US, not Canadian, and I was a US-centric dork for not paying more attention earlier (which you'd think I wouldn't be, living all of three hours from Canada, but no... /facepalm :)). but I'll leave here for other reference use.)

you can only deduct the extra expenses of the cost of gluten free foods (like, how much more a loaf of gluten-free bread costs than equivalent regular bread) IF you can file medical deductions, meaning your medical expenses total 7.5% of your adjusted gross income. if your adjusted gross income is $40k, that means you have to document $3k of post insurance medical expenses. additionally, many accountants note that taking a deduction for the cost of food is likely to set you up for an audit, because that is a grey area - and it can be argued whether or not specialty products are necessary or a luxury.


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



Celiac.com Sponsor (A8-M):



maile Newbie
(just want to clarify the tax thing...)

you can only deduct the extra expenses of the cost of gluten free foods (like, how much more a loaf of gluten-free bread costs than equivalent regular bread) IF you can file medical deductions, meaning your medical expenses total 7.5% of your adjusted gross income. if your adjusted gross income is $40k, that means you have to document $3k of post insurance medical expenses. additionally, many accountants note that taking a deduction for the cost of food is likely to set you up for an audit, because that is a grey area - and it can be argued whether or not specialty products are necessary or a luxury.

just a note, tarnalberry, your information is for US patients (eta, that sounded a little snippy, sorry tarnalberry, not my intention :blink: ), nb-canada is Canadian and the rules are somewhat different due to differing tax regimes. In Canada medical expenses:

Medical expenses for the taxpayer, the taxpayer's spouse or common-law partner, and dependent children under 18 are claimed on line 330 of the federal tax return. Only expenses in excess of the lesser of $1,925 (federal, for 2007) or 3% of net income can be claimed. The lowest tax rate is applied to the medical expenses to determine the amount of the tax credit.

the specifics on claiming for Celiac (for which you do require an official diagnosis) can be found here: Open Original Shared Link

tarnalberry Community Regular

ooo! thanks! I'm apparently a little slow this morning. :D

curiousgeorge Rookie

I sent you a PM.

Those are not celaic tests by any stretch. I really hope you didn't pay for them :(

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. - catnapt replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      8

      how much gluten do I need to eat before blood tests?

    2. - trents replied to SilkieFairy's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      IBS-D vs Celiac

    3. - trents replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      8

      how much gluten do I need to eat before blood tests?

    4. - SilkieFairy posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      IBS-D vs Celiac

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

    • Total Members
      133,321
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • catnapt
      oh that's interesting... it's hard to say for sure but it has *seemed* like oats might be causing me some vague issues in the past few months. It's odd that I never really connect specific symptoms to foods, it's more of an all over feeling of unwellness after  eating them.  If it happens a few times after eating the same foods- I cut back or avoid them. for this reason I avoid dairy and eggs.  So far this has worked well for me.  oh, I have some of Bob's Red Mill Mighty Tasty Hot cereal and I love it! it's hard to find but I will be looking for more.  for the next few weeks I'm going to be concentrating on whole fresh fruits and veggies and beans and nuts and seeds. I'll have to find out if grains are truly necessary in our diet. I buy brown rice pasta but only eat that maybe once a month at most. Never liked quinoa. And all the other exotic sounding grains seem to be time consuming to prepare. Something to look at later. I love beans and to me they provide the heft and calories that make me feel full for a lot longer than a big bowl of broccoli or other veggies. I can't even tolerate the plant milks right now.  I have reached out to the endo for guidance regarding calcium intake - she wants me to consume 1000mgs from food daily and I'm not able to get to more than 600mgs right now.  not supposed to use a supplement until after my next round of testing for hyperparathyroidism.   thanks again- you seem to know quite a bit about celiac.  
    • trents
      Welcome to the celiac.com community, @SilkieFairy! You could also have NCGS (Non Celiac Gluten Sensitivity) as opposed to celiac disease. They share many of the same symptoms, especially the GI ones. There is no test for NCGS. Celiac disease must first be ruled out.
    • trents
      Under the circumstances, your decision to have the testing done on day 14 sounds very reasonable. But I think by now you know for certain that you either have celiac disease or NCGS and either way you absolutely need to eliminate gluten from your diet. I don't think you have to have an official diagnosis of celiac disease to leverage gluten free service in hospitals or institutional care and I'm guessing your physician would be willing to grant you a diagnosis of gluten sensitivity (NCGS) even if your celiac testing comes up negative. Also, you need to be aware that oats (even gluten free oats) is a common cross reactor in the celiac community. Oat protein (avenin) is similar to gluten. You might want to look at some other gluten free hot  breakfast cereal alternatives.
    • SilkieFairy
      After the birth of my daughter nearly 6 years ago, my stools changed. They became thin if they happened to be solid (which was rare) but most of the time it was Bristol #6 (very loose and 6-8x a day). I was on various medications and put it down to that. A few years later I went on this strict "fruit and meat" diet where I just ate meat, fruit, and squash vegetables. I noticed my stools were suddenly formed, if a bit narrow. I knew then that the diarrhea was probably food related not medication related. I tried following the fodmap diet but honestly it was just too complicated, I just lived with pooping 8x a day and wondering how I'd ever get and keep a job once my children were in school.  This past December I got my yearly bloodwork and my triglycerides were high. I looked into Dr. William Davis (wheat belly author) and he recommended going off wheat and other grains. This is the first time in my life I was reading labels to make sure there was no wheat. Within 2 weeks, not only were my stools formed and firm but I was only pooping twice a day, beautiful formed Bristol #4.  Dr. Davis allows some legumes, so I went ahead and added red lentils and beans. Nervous that the diarrhea would come back if I had IBS-D. Not only did it not come back, it just made my stools even bigger and beautiful. Still formed just with a lot more width and bulk. I've also been eating a lot of plant food like tofu, mushrooms, bell peppers, hummus etc which I thought was the cause of my diarrhea before and still, my stools are formed. In January I ran a genetics test because I knew you had to have the genes for celiac. The report came back with  DQ 2.2 plus other markers that I guess are necessary in order for it to be possible to have celiac. Apparently DQ 2.2 is the "rarer" kind but based on my report it's genetically possible for me to have celiac.  I know the next step is to bring gluten back so I can get testing but I am just not wanting to do that. After suffering with diarrhea for years I can't bring myself to do it right now. So that is where I am!   
    • catnapt
      learned I had a high PTH level in 2022 suspected to be due to low vit D  got my vit D level up a bit but still have high PTH   I am 70 yrs old (today in fact) I am looking for someone who also has hyperparathyroidism that might be caused by malabsorption    
×
×
  • 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.