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 Celiac.com!
    eNewsletter
    Donate

Tested


stbakjj

Recommended Posts

stbakjj Newbie

ok so im new here and just have a question for everyone. my son is diabetic and is tested for celiac once a year. the 1st blood test came back positive, so a few months later we did an endoscope. that came back neg. the doctor told us that it still didnt put us in the safe zone but not to worry and come back in a year. instead of waiting we went and got the gene test. the doctor told us that he doesnt have celiac but he has the gene which means he will probably get celiac at some point in his life. they told us to just let him eat normally and watch for any symptoms. so i guess my question is is this good advice? he has never had symptoms and hasnt started showing any as of now. should we test him every year or just hang out and wait? just confused and looking for anyone who can help!! :unsure:

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



CarlaB Enthusiast

If the blood test came back positive, he is reacting to the gluten, it just hasn't damage the intestine yet!! What you are doing is waiting till there is damage. I don't know why docs think this is the "right" was to test -- seems to me that if someone is reacting to gluten the doc would want them to PREVENT the damage! In all other diseases -- heart disease, cancer, etc. -- we talk about prevention, except celiac! :blink:

Okay, a little sarcasm there, sorry ... I'd take him off gluten because of the blood test. Why wait?

Welcome!

Link to comment
Share on other sites
jerseyangel Proficient

Hi and welcome to the board! :)

I agree with everything Carla said--why wait until there is visable damage? I would definately begin the gluten-free diet now. Plus, the endoscope/biopsy can always miss damage, especially in the early stages.

Link to comment
Share on other sites
Nancym Enthusiast

Most doctors don't/aren't recognizing that there is a phase of the disease before celiac. We call it gluten sensitivity. Your risk of autoimmune disease, cancers and other things are a lot higher. I suggest going to enterolab.com and reading up on it. Another source I recommend is the book "Dangerous Grains".

Link to comment
Share on other sites
aprilh Apprentice
ok so im new here and just have a question for everyone. my son is diabetic and is tested for celiac once a year. the 1st blood test came back positive, so a few months later we did an endoscope. that came back neg. the doctor told us that it still didnt put us in the safe zone but not to worry and come back in a year. instead of waiting we went and got the gene test. the doctor told us that he doesnt have celiac but he has the gene which means he will probably get celiac at some point in his life. they told us to just let him eat normally and watch for any symptoms. so i guess my question is is this good advice? he has never had symptoms and hasnt started showing any as of now. should we test him every year or just hang out and wait? just confused and looking for anyone who can help!! :unsure:

Okay, so I just don't agree with that dr. at all!!!!! I think if he tested positive and has the gene you will be setting him up for failure to keep feeding him wheat. The symptoms come on slow and are a lot of times unrelated (by the dr.s) to celiac. It's very hard to diagnose. You may even notice his diabetes start to improve once you get him off the wheat. If that were my child, I would just go ahead and put him wheat free. You can do so much damage to your body if you wait until they "diagnose" him.

How does the gene test work? I was thinking of testing my kids.

Link to comment
Share on other sites

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      121,201
    • Most Online (within 30 mins)
      7,748

    Sohaib Askar
    Newest Member
    Sohaib Askar
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      So, I contacted Scott Adams, the author of that article and also the creator/admin of this website, and pointed out to him the need to clarify the information in the paragraph in question. He has now updated the paragraph and it is clear that the DGP-IGA does serve the purpose of circumventing the false negatives that IGA deficiencies can generate in the tTG-IGA antibody test.
    • knitty kitty
      Here's a link... Thiamine Deficiency Causes Intracellular Potassium Wasting https://www.hormonesmatter.com/thiamine-deficiency-causes-intracellular-potassium-wasting/
    • Soleihey
      Has anyone experimenced enlarged lymph nodes with celiac? Both in the neck and groin area. Imaging of both areas have said that lymph nodes are reactive in nature. However, they have been present for months and just wondering how long this may take to go down. Been gluten-free for about two months. Blood counts are normal.
    • Kmd2024
      Hmm interesting I just assumed that any “IGA” tests including the DPG iga would be negative in a person who is IGA deficient but maybe that is not the case for the DPG test.
    • Scott Adams
      If you were just diagnosed I can say that if you go 100% gluten-free should should see dramatic improvement of your symptoms over the next few months, but the hard part is to stay gluten-free. This article has some detailed information on how to be 100% gluten-free, so it may be helpful (be sure to also read the comments section.):    
×
×
  • Create New...