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

3 year old blood testing


Shantaythomas16

Recommended Posts

Shantaythomas16 Rookie

My 3 year old is having blood testing. She is low weight. She has chronic constipation and extreme distended abdomen since she began eating table food. I have celiac disease so I requested her GP to test her. She said she was having the celiac panel done but when results came through on the online panel, the only test that showed up said “Immunoglobulin A Quan.” Her result was 22 which was in the normal range for that hospital. I’m assuming that was the Total iGA test right? Her doctor said it was negative for celiac disease but that was the only test ran. When I had my testing done at 15, all of my tests were normal range aside from my DGP IGG which was high. Then I had a positive biopsy. Is it possible her GP just doesn’t know what she is doing? When I told her which test was positive on me she says oh Well I’ll add that one but her celiac test was negative. Am I right? Is the “Immunoglobulin A Quan.” A Total IGA test? The reference range was 19-102 


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



Celiac.com Sponsor (A8-M):



cyclinglady Grand Master

Yikes!  Get another doctor, if she refuses to order a complete panel.  Maybe get a new one anyway.  What else could this doctor be missing?  There is no excuse for a doctor not to google the tests.  Shameful!  Only a few celiacs are actually Immunoglobulin A (IgA) deficient.  They use the test to validate the “IgA” Type celiac tests (it is called a control test).  
Like you, I test positive to only the DGP IgA (not IgG) and am biopsy confirmed.  I’d have tested my kid twice so far and I insisted on a complete celiac panel.  Her doctor never balked.  A positive on the DGP is weird, I admit.  But not for little kids.  The DGP Tests are better for them.  Google it.  
 

Mayo Clinic just did a study.  Instead of 1 in 10 rush for developing celiac disease when you have a first degree relative, they found a 44% chance!  Yikes!  
 

https://newsnetwork.mayoclinic.org/discussion/mayo-clinic-study-calls-for-screening-of-family-members-of-celiac-disease-patients/

Shantaythomas16 Rookie
1 hour ago, cyclinglady said:

Yikes!  Get another doctor, if she refuses to order a complete panel.  Maybe get a new one anyway.  What else could this doctor be missing?  There is no excuse for a doctor not to google the tests.  Shameful!  Only a few celiacs are actually Immunoglobulin A (IgA) deficient.  They use the test to validate the “IgA” Type celiac tests (it is called a control test).  
Like you, I test positive to only the DGP IgA (not IgG) and am biopsy confirmed.  I’d have tested my kid twice so far and I insisted on a complete celiac panel.  Her doctor never balked.  A positive on the DGP is weird, I admit.  But not for little kids.  The DGP Tests are better for them.  Google it.  
 

Mayo Clinic just did a study.  Instead of 1 in 10 rush for developing celiac disease when you have a first degree relative, they found a 44% chance!  Yikes!  
 

https://newsnetwork.mayoclinic.org/discussion/mayo-clinic-study-calls-for-screening-of-family-members-of-celiac-disease-patients/

Thank you! It makes me feel better to know I was not wrong on thinking they weren’t running the correct test! From what I understood the Total IGA was supposed to be normal in order for the TTG IGA to be correct. And for you doing toddlers or Infants it’s better to do the DGP testing. Her GP said she added on another test after I explained my test results but I honestly have no clue which test it is they added or if they even know which test they are supposed to do. I’m so frustrated. I’m just going to focus my energy into getting her a referral to a GI. 

cyclinglady Grand Master

Here is my advice.  Get the medical records.  Print off or save every lab report you get online.  It can be so useful in the future.  I have all my medical records going back 25 years, for me and my family.  When I change doctors, I bring in a family health history (tree diagram).  Every doctor loves it and so do my sister-in-laws!   I also have a single page health history.  Again, with a glance, new doctors can easily continue treatment.  Of course, I have the lab records to support all this health history.  
 

Push for the GI consult.  At the very least, talk to your own GI for advice.  I hate to see your child sick.  My daughter was only 5% in weight but 50% in height and head circumference.  But my whole family is little.  She was thriving.  It sounds like your daughter is not.  😢

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now

  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,165
    • Most Online (within 30 mins)
      7,748

    melindakathleen
    Newest Member
    melindakathleen
    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...