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

Help With Analysis Results


juhuu

Recommended Posts

juhuu Newbie

In my country celiac disease is not so known and doctors dont know to much about that disease.

This is my analysis results:

negative anti gliadin IgA and very high positive IgG

positive Tissue Transglutaminase IgG

Can anyone tell me is that good or bad ?

On analysis before this everything where positive, so any progress since then?

Thanks.


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



Celiac.com Sponsor (A8-M):



mushroom Proficient

Without knowing the actual numbers on your tests it is hard to tell if you are making any progress. Also, how long ago was your first round of testing. If your numbers are not dropping at all you are not making any progress, although interesting that the IgA was now negative. You could be a low IgA producer - you don't mention if total IgA was run.

juhuu Newbie

Here are my latest results:

date of analysis: Jul 5

Anti gliadin IgA :1.21 U/ml

Anti Gliadin IgG : 22.76 U/ml

Tissue Transglutaminase IgG: 3.56 U/ml

My first results:

date of analysis:March 26

Anti gliadin IgA :7.78 U/ml

Anti Gliadin IgG : 39.59 U/ml

Tissue Transglutaminase IgG: 3.39 U/ml

After these first results, gastroscopy results confirmed that I have celiac disease. I started with gluten-free diet from 27 April. Do these results show progress according to my diet?

kareng Grand Master

I'm not an expert, but they look like they are coming down. It can take longer than 2 months for them to go back to normal.

mushroom Proficient

It is normal to do this kind of check after six months and a year. People heal at different rates and a three-month check doesn't really mean a lot. Many of us have barely begun to heal at that point.

  • 9 months later...
downtownjodiebrown Newbie

Hi, at 50 yrs old I just got diagnosed after 45 yrs of symptoms. So I was happy to at least get the diagnosis. I was tested in Oct 2012 while still eating some gluten.

My IgA was 474

I have been gluten free for 3 months. Have been also drinking an  intestinal healing powder for celiacs and also taking lots of Bio K liquid probiotics as I also have a candida issue on top of the celiacs.

Other than the celiacs and candida, I am a health nut except for my sweet tooth. I juice,eat sardines,taking vitamin,E,A,D and zinc.The rashes (chicken pox like)  that have ravaged  my scalp and buttocks for 35 years are both almost gone after going gluten free the last three months so imagine my horror to see this result on Mondays IgA test on my celiacs panel.

My IgA  is now 519 !!!!! should I be dead ? I see everyone else with numbers below 130. and I'm getting scared. I do believe my current Dr is a moron though. she knows very little about eliacs and look s at me like she thinks I am lying about all the symptoms I have had. I want a new Dr in the Denver area. I saw on this site there was a Celiacs Dr nearby so Halleluyah !!! Thanks for posting that !

Archived

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

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

    • Total Members
      133,428
    • Most Online (within 30 mins)
      7,748

    twin68grcom
    Newest Member
    twin68grcom
    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
      just a few days off of that drug and my digestive system is finally getting back to normal stopping the gluten challenge was not enough to get back to normal, I was still horribly constipated with what seemed like a paralyzed digestive track- nothing was moving! but now, with a few mag citrate capsules that I had to order online and stopping the chlorthalidone, things are getting back to my usual "working well" digestion   so it's clear that the symptoms I had during the gluten challenge were compounded by the new med that was started the same day (I feel like the Dr really should have known better than to do those two things at the same time, add a new drug and start a new diet protocol... but I'm just the patient, what do I  know, right?)   I am going to do another 24 hr urine in a few weeks to see if lowering the dose of vit D gets my urine calcium down to a more tolerable level. that's the plan.  hope it works.  
    • Wheatwacked
    • catnapt
      oh geez!! i made a whole long detailed post and it didn't save it   I give up grrrrrrrrrrr  
    • catnapt
      I'm not delaying my recovery- I was well on my way to recovering, IF I do have celiac disease by listening to my body and not eating the foods that made me feel ill. the drug I just stopped taking was making me incredibly ill and it's unfortunate and more than  a little frustrating that the dr  
    • Wheatwacked
      Click on the image to make it larger.  Maybe doesn't work on phone browser,  That was from 2021. Absolutely, they should be tested, The point is you have symptoms that the doctors don't understand and malabsorption may be the cause.   Not trying to.  But much of your rant includes refeferences that may indicate multiple nutritional deficiencies.     Some countries also have tax incentives and financial aid for Celiacs.   Celiac disease is recognized as a disability under the ADA because it substantially limits major life activities like eating and digestive function. Protections require reasonable accommodations in public accommodations, including schools (504 plans), colleges, and hospitals. These often include providing safe, gluten-free food, though they do not force restaurants to provide it.  As far as your recovery, eat gluten free.  Get healthier now and worry about diagnosis later.  Many here on the forum have gone ten or more years looking for a diagnosis, with many doctors and many misdiagnosis along the way. It really doesn't matter why, but you cannot eat  gluten.  That is what is important.  With gluten out of the way, maybe the doctors can make sense of your remaining symptoms.  If you need the ADA, then a medical diagnosis is the way to go.  Meantime you are delaying your recovery from whichever celiac disease or NCGS and the inevitable step one of Gluten Free Diet. tWe come to share experiences and maybe it will help someone. In reality, I don't care.  By the way I have stopped 6 medications Against Medical Advice because they did not do their job and the side effects were crippling. This is a lifelong fight for your life.  Pick you battles carefully.  Assume the worst, celiac disease, and deal with it.  Denial is not just a river in Egypt. Pleased to meet you, too.  
×
×
  • 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.