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

Blood Tests


Wi11ow

Recommended Posts

Wi11ow Apprentice

I can't thank you all enough for the information and inspiration on this website. I haven't been able to get any blood tests done to this point.

 

I printed off information I got from people here. I wouldn't have found these websites without you! From the University of Chicago Celiac Disease Center and  NIH and the Wm K. Warren Medical Research Center for Celiac Disease at UC San Diego. and brought it all with me to my doctor. Symptoms, that the biopsy should have been 4-6 samples (not 1), which tests to do.....

 

I told him I had the biopsy but with only one sample and I wanted to have the C blood panel done. I was armed with the list many people have posted here.  He kept saying, wow, you have done your research. You have really done your homework. At one point he said he knew that C was in the top 10 most mis diagnosed diseases.

 

He did these and a couple others. CNA I think and I don't remember what else

  • tTG IgA and IgG
  • DGP IgA and IgG
  • EMA IgA 
  • total serum IgA
  • AGA IgA and AGA IgG

 

 

I just wanted to say thanks for the support and helpful information. I probably wouldn't have kept pushing for tests with out it... It will take about 10-14 days for results.

 

L

 

 


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



Celiac.com Sponsor (A8-M):



nvsmom Community Regular

Good luck with the tests!  :)

Fenrir Community Regular

Glad you got the testing that will help determine if Celiac is the problem or not.

Wi11ow Apprentice

I had a dermatology appt this morning follow up from skin cancer biopsies 2 months ago. One was of some concern but non malignant. Got the all clear today! YEAh! And I don't have arthritis. (This is the short version) :)

 

While I was out, I stopped by my doc's office to get a print out of the exact blood tests that were run last week. I don't know why I am not smart enough to do this while I am there!!! Doc came out and said - great news! Your tests are negative. (bare with me there more) I had mixed feelings, I want to know what's wrong! They hand me a sheet of paper, it says

 

Anti Nuclear Antibody          Negative

Rheumatoid Factor Screen     Negative

 

Hmmm.  I said - Do you think I could get a print out of exactly what was tested? For my records? She tells me some information, but I said well, this doesn't say anything about what was done. What antibodies were tested? Then I get handed a brochure - This has everything that was tested. I start reading..... It's all about cholesterol. :angry:

 

I asked again - what exactly is Anti Nuclear Antibody? She asks nurse - it's testing for arthritis. 

I said - I thought you ran a full test for Celiac? What about Itt IgE, IgA? (I don't have any information with me, I just stopped in to get a print out!!)

Nurse comes back up to the front to talk to me

 

She says - your information hasn't been scanned in so i can't print it out, but here is a blank form of what would have been tested AND WE ADDED IN Miroalbumim (no idea what this is), magnesium and CELIAC.

 

A tiny little twisted light bulb goes on in my head... I said - so you haven't got the test results back yet. :blink:

She said NO! Ok - so my tests aren't all negative. You don't know yet!

 

I put a grin on my face - OK, I will just wait for your call.

 

 

WOW, that was painful!  <---------------beating head against wall laughing!!

 

New favorite saying George Bernard Shaw - "The single biggest problem in communication is the illusion that it has taken place." I need to put this in my sig line.

 

Day 9 gluten soy, etc free. New outlook - I didn't get mad, spooled up, upset. Just Kept asking what tests were run over and over. It's kind of funny really.

 

My new motto - When did I learn to speak Greek??!?

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      126,136
    • Most Online (within 30 mins)
      7,748

    kfkynett
    Newest Member
    kfkynett
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.9k
    • Total Posts
      69.2k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • StaciField
      There’s a Cosco in Auckland in New Zealand. It’s a bit away from where I live but it’s worth the travel for me. Very appreciative of your advice.
    • Wheatwacked
      It seems you have proven that you cannot eat gluten.  You've done what your doctors have not been able to do in 40 years. That's your low vitamin D, a common symptom with Celiac Disease.  Zinc is also a common defiency.  Its an antiviral.  that's why zinc gluconate lozenges work against airborne viruses.  Vitamin D and the Immune System+ Toe cramps, I find 250 mg of Thiamine helps.   When I started GFD I counted 19 symptoms going back to childhood that improved with Gluten Free Diet and vitamin D. I still take 10,000 IU a day to maintain 80 ng/ml and get it tested 4 times a year. Highest was 93 ng/ml and that was at end of summer.  Any excess is stored in fat or excreted through bile.   The western diet is deficient in many nutrients including choline and iodine.  Thats why processed foods are fortified.  Celiac Disease causes malabsorption of vitamins and minerals from the small intestine damage.  GFD stops the damage, but you will still have symptoms of deficiency until you get your vitamins repleted to normal.  Try to reduce your omega 6:3 ratio.  The Standard American Diet is 14:1 or greater.  Healthy is 3:1.  Wheat flour is 22:1.  Potatoes are 3:1 while sweet potatoes are 14:1.  So those sweet potatos that everyone says is better than Russet: they are increasing your inflammation levels.   
    • John.B
      Hello, Target recently changed their branding on the Up & Up Loratadine and no long have it labeled gluten free. I've not been able to find any meds labeled gluten free for allergies. Some lists showed them but the the packaging isn't labeled.  Wondering if anyone knows of or has a list that would be safe for Celiac kiddos.
    • Scott Adams
      My mother also has celiac disease, and one of her symptoms for many years before her diagnosis was TMJ. I believe it took her many years on a gluten-free diet before this issue went away.
    • Jeff Platt
      Ear pain and ringing your entire life may or may not be TMJ related but could be something else. A good TMJ exam would be helpful to rule that out as a potential cause from a dentist who treats that. I have teens as well as adults of all ages who suffer from TMJ issues so it’s not a certain age when it shows up.   
×
×
  • Create New...