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

Enterolab


Guest cassidy

Recommended Posts

Guest cassidy

I had a negative blood test and negative biopsy, but very positive dietary reactions. I keep going back and forth on how important it is to get an official diagnosis. I'm sticking to my diet, but I would like some sort of confirmation.

Has anyone gone to Enterolab when they had symptoms and a negative blood test and gotten a negative result withe Enterolab? Was the testing covered by insurance? Did you feel it was a good use of money? Were you happy with their professionalism and the testing procedure?


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



Celiac.com Sponsor (A8-M):



teankerbell Apprentice

My stool test from Enterolab came back positive, but blood results were negative. So conflicting results. My doctor says that test results are not always reliable and feels that if you feel better off gluten then you have your answer.

How long have you been gluten-free? If you happen to be gluten-free for over 8 months, the stool test could come out negative.

I did not use insurance to pay for the lab test, but our FSA (flex spend account). I feel it was worth it because I also found out I am casein intolerant.

dlp252 Apprentice

There have been a couple of people that I can remember on the boards who had a negative test from Enterolabs, but I'm not sure they're still posting here. If I can find the posts I'll post a link. The Enterolab website says you can be gluten-free for about a year and their test will still find the antibodies. I never went the traditional way of testing because I had been on a low carb diet for a couple of years, so figured the tests wouldn't catch anything anyway, so I went directly to Enterolabs. I didn't submit it to my insurance so don't know if they would have paid, I do, however, think it was worth it for me to know for sure (I tend to rationalize away the good common sense I should have about my diet, so to have something concrete keeps me on the right path).

Okay, here's the recent one I was thinking of:

Open Original Shared Link

jnclelland Contributor
Has anyone gone to Enterolab when they had symptoms and a negative blood test and gotten a negative result withe Enterolab? Was the testing covered by insurance? Did you feel it was a good use of money? Were you happy with their professionalism and the testing procedure?

(raises hand) That would be me! I finally decided to do Enterolab after about 8 months gluten-free, and everything came back negative - except for the gene test, which showed that I have one celiac gene and one gene for non-celiac gluten-sensitivity. Two of the tests were towards the high end of the negative range, and I *suspect* that they might have been positive if I had done the test sooner after going gluten-free - but of course I'll never know!

It wasn't covered by my insurance. I wish it weren't so expensive, and I'm a bit frustrated that it game back negative, because what I *really* wanted was some sort of diagnosis. But they were very professional, and one of the nurses sent me a nice email response to my questions about what the "high negative" really meant (basically, she said that it's entirely possible it would have been a low positive 8 months ago, but there's no way to know for sure). And I am glad to have the results of the genetic testing, because now I KNOW that my kids will each have a gene for gluten sensitivity of some sort, and it's something definite that I can tell their ped if I ever decide I want to get them tested. (I'm actually considering having my son tested, but he doesn't really have any severe symptoms, just a few little things that make me wonder. So I'm still on the fence about it...)

Jeanne

slpinsd Contributor

I had only a positive IgG with blood, and with Enterolab, I had a positive IgA. They test both Antigliadin IgA and Antigliadin Transglutaminase.

The gene testing was very helpful, showing 2 copies of the Celiac Gene. For that it was worth the money.

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. - marlene333 replied to Grace Good's topic in Gluten-Free Foods, Products, Shopping & Medications
      3

      Bee balm lipbalm not gluten free

    2. - Mari replied to Jmartes71's topic in Coping with Celiac Disease
      4

      Related issues

    3. - Scott Adams replied to catsrlife's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      4

      Patiently Waiting to See Results

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

      Patiently Waiting to See Results

    5. - Jmartes71 replied to Jmartes71's topic in Coping with Celiac Disease
      4

      Related issues


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,261
    • Most Online (within 30 mins)
      7,748

    Pbaentine
    Newest Member
    Pbaentine
    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

    • marlene333
      To play it safe, use Vasoline Lip Therapy. No questions as to it containing gluten.
    • Mari
      jmartes, Thank you for sharing  more information with us. Most of us Celiacs whose problems do not clear up with in a few years have to decide what to do next. We can keep seeing DR.s and hope that we will get some  medication or advice that will improve our health. Or we can go looking for other ways to improve our health. Usually Celiac Disease is not a killer disease, it is a disabling disease as  you have found out. You have time to find some ways to help you recover. Stay on your gluten-free diet and be more careful in avoiding cross contamination . KnittyKitty  and others here can give you advice about avoiding some foods that can give you the gluten auto immune reaction and advice about vitamins and supplement that help celiacs. You may need to take higher doses of Vit. B12  and D3.  About 20 years before a Dr. suggested I might have Celiac disease I had health problems that all other Dr said they could not identify or treat. I was very opposed to alternative providers and treatments. So many people were getting help from a local healer I decided to try that out. It was a little helpful but then, because I had a good education in medical laboraties she gave me a book  to read and what did I think. With great skeptism I started reading and before I was half way through it I began using the methods outlined in the book. Using those herbs and supplements I went from hardly able to work to being able to work almost fulltime. I still use that program. But because I had undiagnosed celiac disease by 10 years later some  of my problems returned and I started to loose weight.    So how does a person find a program that will benefit them? Among the programs you can find online there are many that are snake oil scams and some that will be beneficial. by asking around, as I did. Is there an ND in your area? Do they reccomend that person? If you would like to read about the program I use go to www.drclark.net   
    • Scott Adams
      It's unfortunate that they won't work with you on this, but in the end sometimes we have to take charge of our own health--which is exactly what happened to me. I did finally get the tests done, but only after years of going down various rabbit holes and suffering. Just quitting gluten may be the best path for you at this point.
    • catsrlife
      My doctor didn't take the time to listen to anything. I don't even think she knows what it means. She is more concerned about my blood pressure that is caused by her presence than anything else and just wants to push pills at me. The so-called dermatologist wouldn't do a skin test. she prescribed all of these silly antihistamine skin meds. This lady didn't even know what she was talking about and said "they never turn out as celiac, they usually just say it's dermatitis so here's your meds," just like my regular quack. I'm trying to change insurance companies at the moment and that has been a battle because of red tape, wrong turns, and workers having wrong phone numbers. What a joke! The allergy blood days say I have a wheat allergy of .31. Hopefully it's just that and until I find a decent doctor and dermatologist, I'll just lay off the wheat anyway, since it gives me asthma, high blood sugar, and joint pain. So frustrated at this point. The rash on my back of arms/elbows is mostly gone. Both calves and chest have started up. smh. It comes and goes. It fades faster now, though, although my forearms still produce one or two bumps on each side. The itching has calmed down a lot except for the bump area. I have dry skin to begin with so anything affecting it just makes it crazy. i'm never going to eat wheat again. I don't care if they need it to produce results or if it is just an intolerance, allergy, or celiac. It gives me hell.
    • Jmartes71
      I had the test done by one of the specialist through second pcp I had only a few months because he was saying I wasn't.Even though Im positive HLA-DQ2 .My celiac is down played.I am with new pcp, seeing another girl doctor who wants to do another breathe test next month though Im positive sibo this year.I have high blood pressure not sure if its pain from sciatica or sibo, ibs or hidden gluten. Im in disability limbo and I should have never been a bus driver because im still suffering and trying to heal with zero income except for my husband. This isnt fare that my health is dictating my living and having ti beg for being revalidation of my disregarded celiac disease. Its an emotional roller coaster I don't want to be on and the medical made it worse.New pcp new gi, exhausted, tired and really fed up. GI doctor NOT girl..
×
×
  • 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.