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

Can You Share More About Why You Felt Ok With Using This Lab?


happy4dolphins

Recommended Posts

happy4dolphins Enthusiast

HI,

The process of ordering the tests on line was very easy and paying was also easy.

It's the back and forth information about weather or not it's more relyable then the blood work. IT's a lot of money, but I'm still interested in doing both my daughter and I. WE (hubby and I) are in deabate about weather or not it wil be usedful for us or if knowning that we react to the gluten is enough.

Now our bcbs said that all of those tests were covered based on the diagnosis they gave, provided it was from an approved lab. Entero Las wasn't on the "approved" list fro bcbs ppo.

SO, I did call the rheumatologist to talk with her and she said she'd done the celiac tests. But I got an e mail from someone saying that I need to ask for a celiac panel test. I would have thought the rheumy would have known to do that. SO there's some confusion there about why it wasn't done.

I do have both of the packages from Enterolab here, so If I change my mind. I"m guessing I can just do a reorder!?!???? I've been thinking maybe I'll do one now for me and do another one for megan later if I can't find any other approved labs here.

Now, does WHY is ENtero lab different, other then being in Texas?

Nicole


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



Celiac.com Sponsor (A8-M):



CarlaB Enthusiast

For me, I was gluten-free because I had figured out on my own that gluten was a problem. After some time gluten-free, I was still sick and wanted a celiac test. Now I know I wasn't really gluten-free because of hidden gluten and contamination.

The doc tested me for IgA only. He just wasn't real familiar with celiac. He also didn't mention that I should be eating gluten for the test. The test was negative. I went to a GI several months later, was more gluten-free at the time as I was finding some of the hidden glutens. He told me to eat maybe a little more gluten than I was and he'd do an endoscopy and colonoscopy in 6 weeks. Now I know six weeks wasn't enough and a little gluten wasn't enough either. Those tests were negative, too, yet I spent that six weeks VERY ill. That should have been enough proof for me!

Since I have kids and knew Enterolab had genetic testing, I just wanted someone to tell me I wasn't crazy. So, I used it. I recommend it to people who either have negative testing yet know they have a reaction, or to someone who is already gluten-free because I think it's ridiculous to go on a gluten challenge (especially after having been on one) if you're feeling better off gluten.

I was happy with their service and my dietary response for both the gluten and the casein proves the test were correct for me. I went into denial about the casein, but eventually had to give it up.

dionnek Enthusiast

I used them to get the genetic test for my 2 year old daughter. I was recently dx with celiac; my daughter does not have any sympotms so the dr's won't test her, so I just decided to get the gene test done so I know if I ahve to worry about it in the future - turns out I do :(

They were very easy to use and their genetic test was cheaper than Kimball labs (the other one I checked out).

celiacgirls Apprentice

I used it for my daughter because I suspected her tummy aches were from gluten but the regular blood tests at the doctor were negative. She was tested several times from the time she was 1 until she was 8. My grandmother had celiac and I had read the blood tests were not reliable. My daughter said she felt better gluten-free but the doctors said she didn't need to be on the diet. They thought she was anxious. I thought if I did the Enterolab test and she was negative, I would finally give up the idea that gluten was behind her troubles. Her test was positive so I tested myself and my other daughter.

We were also positive even though we were unaware of any gastro problems. Enterolab suggested we try the diet and see what happened. My mother is also gluten-free even though her biopsy was negative. She also encouraged me to try the diet. Within 3 days, I could see huge differences in the way I felt. That convinced me to have my daughter try the diet. She also feels much better.

Because we had such success with the gluten sensitivity test, I have gradually had other tests done by Enterolab. It turns out we are all casein intolerant and that has made a difference for us, too. Because their results seem to have worked for us, I trust them. My husband is still somewhat skeptical but even he had the gene test done by them. However, when he came up with 1 celiac gene, he said that made him distrust them even more. But he doesn't argue any more with the results we are seeing by changing our diets.

I did not submit our tests for insurance reimbursement. I like that not being part of our record.

AndreaB Contributor

I was gluten light (due to allergy testing) for 1 1/2 months prior to ordering the enterolab tests. After reading more about enterolab and their test I decided to have it done for our whole family. My doctor was willing to test me but since I had been gluten light (very light) I figured it wouldn't come back positive. Me and my children did not have obvious symtpoms prior to going gluten free. Now we all have stomach distress/intestinal distress until it clears our systems.

One thing I found interesting aside from the genes was that I tested IgG intolerant to gluten, soy and dairy; but only IgA intolerant to gluten and soy. I am dairy free as well due to my allergy/intolerance though.

I also did not submit it for reimbursement. From what I understand insurance doesn't cover much of it unless your deductible has been met.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,207
    • Most Online (within 30 mins)
      7,748

    WAB19
    Newest Member
    WAB19
    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

    • trents
      NCGS does not cause damage to the small bowel villi so, if indeed you were not skimping on gluten when you had the antibody blood testing done, it is likely you have celiac disease.
    • Scott Adams
      I will assume you did the gluten challenge properly and were eating a lot of gluten daily for 6-8 weeks before your test, but if not, that could be the issue. You can still have celiac disease with negative blood test results, although it's not as common:  Clinical and genetic profile of patients with seronegative coeliac disease: the natural history and response to gluten-free diet: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5606118/  Seronegative Celiac Disease - A Challenging Case: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9441776/  Enteropathies with villous atrophy but negative coeliac serology in adults: current issues: https://pubmed.ncbi.nlm.nih.gov/34764141/  Approximately 10x more people have non-celiac gluten sensitivity than have celiac disease, but there isn’t yet a test for NCGS. If your symptoms go away on a gluten-free diet it would likely signal NCGS.
    • Xravith
      I'm very confused... My blood test came out negative, I checked all antibodies. I suppose my Total IgA levels are normal (132 mg/dl), so the test should be reliable. Still, I'm not relieved as I can't tolerate even a single biscuit. I need to talk to my doctor about whether a duodenal biopsy is necessary. But it is really possible to have intestinal damage despite having a seronegative results? I have really strong symptoms, and I don't want to keep skipping university lectures or being bedridden at home.
    • Scott Adams
      They may want to also eliminate other possible causes for your symptoms/issues and are doing additional tests.  Here is info about blood tests for celiac disease--if positive an endoscopy where biopsies of your intestinal villi are taken to confirm is the typical follow up.    
    • Scott Adams
      In the Europe the new protocol for making a celiac disease diagnosis in children is if their tTg-IgA (tissue transglutaminase IgA) levels are 10 times or above the positive level for celiac disease--and you are above that level. According to the latest research, if the blood test results are at certain high levels that range between 5-10 times the reference range for a positive celiac disease diagnosis, it may not be necessary to confirm the results using an endoscopy/biopsy: Blood Test Alone Can Diagnose Celiac Disease in Most Children and Adults TGA-IgA at or Above Five Times Normal Limit in Kids Indicates Celiac Disease in Nearly All Cases No More Biopsies to Diagnose Celiac Disease in Children! May I ask why you've had so many past tTg-IgA tests done, and many of them seem to have been done 3 times during short time intervals?    
×
×
  • 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.