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

Bood Test Results


Guest GrimTribe

Recommended Posts

Guest GrimTribe

Well, I went in to Steele's Dr last Wed and got an order for the IgA test for him. We spent Wed thru Sun giving him all the food he'd been denied since we first began to suspect celiac disease.

OMG...

He was miserable. Weepy, irritable, constipated (again!!!!), belly bloating, leg cramps, vomiting....

I was ready to say screw it by Saturday morning.

So we got the blood test done Monday AM and immediately set about getting him flushed out again. He was on fluids Monday & Tuesday with grapefruit for dinner.

We called today to check on the results and they came back negative. Diva is surprised, I'm not, but we are both terribly disappointed. I mean, we made him sick on purpose so the test would have a better chance of coming out pos and still got scrubbed on it.

This kid has enough ammo in his Guilt Trip Gun to knock me out for the next century. We did try to explain to him why he was suddenly allowed to eat pizza and cinnamon rolls and cake. At 5 all he cares about is PIZZA! CINNAMON ROLLS! CAKE!

So we know our next step is to get him to the GI, that's scheduled for next Wed.

We've already researched Enterolab, and found the panel we want (369.00 +shipping OMG) and we know it has a much better chance of successfully locating the celiac disease, but we don't have the funds for it. All we can do it keep him gluten-free and watch for cross contamination.

Diva had her daughter tested too, but we haven't gotten those results yet. I plan to get all of my kids blood tested at least, and myself as well. I really want to know if I have the gene.

Moving Right Along... :(


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



Celiac.com Sponsor (A8-M):



nikki-uk Enthusiast

Had your son been gluten-free for any length of time prior to the blood test??

If so this would be why he got a negative result as you are supposed to be on a high gluten diet for at least 6 weeks before any tests :)

Jestgar Rising Star
Well, I went in to Steele's Dr last Wed and got an order for the IgA test for him. We spent Wed thru Sun giving him all the food he'd been denied since we first began to suspect celiac disease.

OMG...

He was miserable. Weepy, irritable, constipated (again!!!!), belly bloating, leg cramps, vomiting....

I was ready to say screw it by Saturday morning.

Isn't this enough of a diagnosis for you?

Nantzie Collaborator

I wanted to mention that Enterolab has JUST the gluten stool test for $99. It might not be the full panel, but it will give you an answer sooner than waiting to afford the whole thing. That's what I did for my kids.

Nancy

jen2be2 Explorer

I am sorry that this is taking a long time for you and your son.

Have you thought about getting the genetic cheek swab test? We did ours through Kimball genetics. It cost us around 300.00 and it let us know that our son that did not have any antibodies in his blood is a carrier for celiac disease. ( the company that we went through gives a small mulitple family testing discount on the tests~ but a little is better than none ).

We had the results from the test within 3 days of sending it back. Their customer service was great! They also were able to give me and my DH a profile of our DNA genes for celiac based on the test from our DD and DS. We found out that on gene 6 we both had one normal gene and we both had another that was a carrier for celiac disease.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,566
    • Most Online (within 30 mins)
      7,748

    Rrenee2990
    Newest Member
    Rrenee2990
    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

    • cristiana
      That's great news, you can do this.  Let us know how things go and don't hesitate to ask if you have any more questions. Cristiana 😊
    • petitojou
      Thank you so much for sharing your experience and I found myself giggling with happiness as I read how your body reached such spring! And I hope that your current journey is also successful!! Definitely starting the food diary! So many amazing advices. And it’s very scary. It really hits all our soft spots as well as our confidence system. Most doctors I went thought I was underage despite being in my late 20s. Right now I look like am I twelve, but is also this body that’s taking so much, so I might as well love it too! Going to make the necessary changes and stay in this path. Thank you again! 🫶
    • petitojou
      Thank you so much for the information and kind message! Reading this transformed how I’ve been viewing my efforts and progress. Guess there’s still a lot to celebrate and also heal 😌  Yes, I’ve been taking it! Just recently started taking a multivitamin supplement and separated vitamin D! I also took chewable Iron polymaltose for ferritin deficiency 2 months ago but was unable to absorb any of it.  Thank you again! Hearing such gentle words from the community makes my body and heart more patient and excited for the future. 
    • ckeyser88
      I am looking for a roomie in Chicago, Denver or Nashville! 
    • Scott Adams
      Your post demonstrates the profound frustration and isolation that so many in the Celiac community feel, and I want to thank you for channeling that experience into advocacy. The medical gaslighting you endured for decades is an unacceptable and, sadly, a common story, and the fact that you now have to "school" your own GI specialist speaks volumes about the critical lack of consistent and updated education. Your idea to make Celiac Disease a reportable condition to public health authorities is a compelling and strategic one. This single action would force the system to formally acknowledge the prevalence and seriousness of the disease, creating a concrete dataset that could drive better research funding, shape medical school curricula, and validate the patient experience in a way that individual stories alone often cannot. It is an uphill battle, but contacting representatives, as you have done with Adam Gray, is exactly how change begins. By framing it as a public health necessity—a matter of patient safety and protection from misdiagnosis and neglect—you are building a powerful case. Your voice and your perseverance, forged through thirty years of struggle, are exactly what this community needs to ensure that no one else has to fight so hard just to be believed and properly cared for.
×
×
  • 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.