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

Home testing kit


Sally6

Recommended Posts

Sally6 Newbie

I had a light bulb moment a few weeks ago and wondered if I was gluten sensitive/celiac. I'm 58 and probably have suffered from this all my life!!  So decided to cut out glutten for 4 days, what a difference I felt like a new woman. 

 

But then i started googling and realised  I needed to be on gluten for 6 weeks for a reliable result. So I'm back on it and all my symptoms are back. 

 

I bought a home testing kit as I was impatient. I was celiac negative after 10 minutes but celiac positive after 30 minutes.

im still eating gluten but was interested if anyone else had experienced this. 

 

Thanks a lot 


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

I don't know if they are reliable or not.  What test did you use?

Sally6 Newbie

Bio card from boots. I'm from the UK.  

kareng Grand Master
6 minutes ago, Sally6 said:

Bio card from boots. I'm from the UK.  

We don't have them here, yet.  Might call the company and ask about the odd result.

cyclinglady Grand Master

So, the Biocard is a start.  Now, you should get into your GP and ask for a full celiac panel if at all possible.  Bring the biocard results in to show your doctor.  Keep eating gluten until you get all testing done (more blood tests and an endoscopy to obtain biopsies of the small intestine.  

Good luck!  

GFinDC Veteran

Hi Sally6,

The Biocard results are good for a certain number of minutes, after which they aren't reliable, per the test kit instructions.  That doesn't mean you don't have celiac disease though.  The Biocard test only measures one antibody type.  There are several more in the complete celiac disease antibodies panel.  If you can get your physician to do the complete celiac panel, it might show IgA or IgG antibodies.  Some people don't show an antibody reaction on one type of antibody, but do on another.  So although the basic common screening test (ttg IgA) does catch most people, it doesn't catch all cases of celiac disease.

Your symptoms do sound like possible celiac disease.  Also, Hashimoto's Thyroiditis is a condition associated (higher risk of getting it) with celiac disease.

You are correct that you need to continue eating gluten until testing is completed.  But only 4 days off gluten should not be a big problem for the tests.  If you can get the testing done soon, that would be great.  Usually the process includes a blood antibodies panel followed by an endoscopy later.  The endoscopy should take 4 to 6 biopsy samples for microscopic review.  They check them for damage to the villi lining of the small intestine cause by celiac disease.

You don't need to eat a lot of gluten each day to keep the antibodies active.  The University of Chicago celiac center recommends 1/2 slice of bread daily.

Welcome to the forum Sally! :)

P.S.  There is a thread titled Newbie 101 stickied to the top of the coping with forum.  It has some good information for beginners.

Sally6 Newbie

Thanks everyone. That's really helpful. My GP is good but wants to wait for the full 6 weeks before he does a blood test. I've got another 5 weeks which feels like a long time at the moment. I can't wait to be gluten free again as I have never felt so well!!

 

will sort out the newbie bit now ?


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



Celiac.com Sponsor (A8-M):



GFinDC Veteran
7 hours ago, Sally6 said:

Thanks everyone. That's really helpful. My GP is good but wants to wait for the full 6 weeks before he does a blood test. I've got another 5 weeks which feels like a long time at the moment. I can't wait to be gluten free again as I have never felt so well!!

will sort out the newbie bit now ?

Good going Sally!  Shoot, I think it took me about 6 months to sort out the gluten-free diet as a newbie.  That's a bummer they won't do the blood test now.  Did the doctor have any comment on the Biocard test?  I am guessing they would want to see the Biocard test done in their office before they would accept it.  I think the Biocard tests are really useful for individuals trying to sort out if there is a problem themselves, before going to a doctor.

Well, now you've got a chance to use up all those remaining bits of gluten in the cupboard.  You could stop eating dairy now, if it is bothering you.   Quite a few celiacs have problems with dairy before going gluten-free.  Going dairy-free won't affect the celiac testing.  But it might relieve some of the symptoms you are having.

 

Sally6 Newbie

From the above advice I have decided to bring forward my blood test at the docs.  It is now scheduled for next Friday. So hopefully my 4 days gluten free a couple of weeks ago, out of 58 years I should get a reliable result. 

Just want a bit of advice prior to the blood test as I don't want to miss the opportunity of them testing for the minimum. I've been under a neuro surgeon this year for tingling legs. He has decided it is fairly  innocutious and labelled it as peripheral neuropathy . He did a blood test for an autoimmune problem and it came back ok. Will it be the same as a celiac blood test?? Any ideas welcome. 

 

Thankyou. 

GFinDC Veteran

Hi Sally,

I don't know what test he did, but it is likely an ANA spot test.  The ANA test can show some autoimmune problems, but it won't diagnose celiac disease.  Celiac disease is diagnosed by anti-gliaden antibodies (AGA) in the bloodstream, and a positive endoscopy showing immune damage to the gut lining.  So, the ANA isn't a bad test to do, it just isn't specific to celiac disease.

Here's a link with the tests for celiac disease:

Open Original Shared Link

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Rogol72 replied to HAUS's topic in Gluten-Free Foods, Products, Shopping & Medications
      8

      Sainsbury's Free From White Sliced Bread - Now Egg Free - Completely Ruined It

    2. - Scott Adams replied to HAUS's topic in Gluten-Free Foods, Products, Shopping & Medications
      8

      Sainsbury's Free From White Sliced Bread - Now Egg Free - Completely Ruined It

    3. - Scott Adams replied to deanna1ynne's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      13

      Inconclusive results

    4. - deanna1ynne replied to deanna1ynne's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      13

      Inconclusive results


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,442
    • Most Online (within 30 mins)
      7,748

    Nony
    Newest Member
    Nony
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Rogol72
      @HAUS, I was at an event in the UK a few years back. I remember ringing the restaurant ahead to inquire about the gluten free options. All I wanted was a few gluten free sandwiches, which they provided and they were delicious. The gluten-free bread they used was Warbutons white bread and I remember mentioning it on this site before. No harm in trying it once. It's fortified with Calcium and Iron. https://www.warburtonsglutenfree.com/warbs_products/white-loaf/ The only other gluten-free bread that I've come across that is fortified is Schar with Iodized salt, nothing else.
    • Scott Adams
      In the U.S., most regular wheat breads are required to be enriched with certain B-vitamins and iron, but gluten-free breads are not required to be. Since many gluten-free products are not enriched, we usually encourage people with celiac disease to consider a multivitamin.  In the early 1900s, refined white flour replaced whole grains, and people began developing serious vitamin-deficiency diseases: Beriberi → caused by a lack of thiamin (vitamin B1) Pellagra → caused by a lack of niacin (vitamin B3) Anemia → linked to low iron and lack of folate By the 1930s–40s, these problems were common in the U.S., especially in poorer regions. Public-health officials responded by requiring wheat flour and the breads made from it to be “enriched” with thiamin, riboflavin, niacin, and iron. Folic acid was added later (1998) to prevent neural-tube birth defects. Why gluten-free bread isn’t required to be enriched? The U.S. enrichment standards were written specifically for wheat flour. Gluten-free breads use rice, tapioca, corn, sorghum, etc.—so they fall outside that rule—but they probably should be for the same reason wheat products are.
    • Scott Adams
      Keep in mind that there are drawbacks to a formal diagnosis, for example more expensive life and private health insurance, as well as possibly needing to disclose it on job applications. Normally I am in favor of the formal diagnosis process, but if you've already figured out that you can't tolerate gluten and will likely stay gluten-free anyway, I wanted to at least mention the possible negative sides of having a formal diagnosis. While I understand wanting a formal diagnosis, it sounds like she will likely remain gluten-free either way, even if she should test negative for celiac disease (Approximately 10x more people have non-celiac gluten sensitivity than have celiac disease, but there isn’t yet a test for NCGS. If her symptoms go away on a gluten-free diet, it would likely signal NCGS).        
    • JoJo0611
    • deanna1ynne
      Thank you all so much for your advice and thoughts. We ended up having another scope and more bloodwork last week. All serological markers continue to increase, and the doc who did the scope said there villous atrophy visible on the scope — but we just got the biopsy pathology report back, and all it says is, “Duodenal mucosa with patchy increased intraepithelial lymphocytes, preserved villous architecture, and patchy foveolar metaplasia,” which we are told is still inconclusive…  We will have her go gluten free again anyway, but how soon would you all test again, if at all? How valuable is an official dx in a situation like this?
×
×
  • 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.