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Enterolab Results

Mally-bug

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Mally-bug Apprentice
Mally-bug
Posted

If any of you out there have had stool tests done by Enterolab, about how long did you have to wait for your results? I know they say that if you don't hear within three weeks to contact them, but I am wondering if it takes them the better part of three weeks to e-mail you the results?Or did you get the results sooner??? I am just looking for your experience with Enterolab so I know what to expect.

Anybody?

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confused Community Regular
confused
Posted

mine were 2 weeks and 1 day

my step-sons was 2 weeks and 2 days

paula

AndreaB Contributor
AndreaB
Posted

My family's was between 2 and 2 1/2 weeks....I forget exactly.

Moustique77 Newbie
Moustique77
Posted

Hi,

I was just diagnosed about 3 months ago. It took enterolab exactly two weeks for diagnosis. Both my wife and mother-in-law also used them and got them exactly two weeks.

EBsMom Apprentice
EBsMom
Posted

Same here - just over 2 weeks. I understand that impatient feeling. Good luck!

zarfkitty Explorer
zarfkitty
Posted

2 weeks for both myself and daughter. I probably checked my email ten times a day that whole 2 weeks, just in case they were early. So I understand. :)

hathor Contributor
hathor
Posted

A bit over two weeks.

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confusedks Enthusiast
confusedks
Posted

Almost 3 weeks to the day. It was a practice in patience.

Kassandra

tmk Explorer
tmk
Posted

I actually had to wait 5 weeks b/c there was a malfunction in one of their refrigeration units due to a large storm that passed by -- so I had to resubmit my sample. They were really nice about it though and when I explained I needed the results before my GI appointment, they made sure I got them in time. After my resubmittal -- I think it was just over 2 weeks.

Good luck -- I know it sucks waiting, but it is worth it! :)

Guest thatchickali
Guest thatchickali
Posted

I hadn't gotten the results for 3 weeks so I called and they said they didn't have my email on file, and my results had been ready a week before. Right at 2 weeks. But if you haven't gotten them, try logging into your account on their website.

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    • Scott Adams
      Test interpretations

      By Scott Adams · Posted

      Based on those results alone, it’s not possible to say you have celiac disease. The test that is usually most specific for celiac, tTG-IgA, is negative in your results, and the endomysial antibody (EMA) is also negative, which generally argues against active celiac disease. However, your deamidated gliadin IgA is elevated, and your total IgA level is also high, which can sometimes affect how the other antibody tests behave. Another important factor is that you were reducing gluten before the test, which can lower antibody levels and make the results less reliable. Because of that, many doctors recommend a gluten challenge (eating gluten regularly for several weeks) before repeating blood tests or considering an endoscopy if symptoms and labs raise concern. It would be best to review these results with a gastroenterologist, who can interpret them in context and decide whether further testing is needed.
    • trents
      Test interpretations

      By trents · Posted

      Since you compromised the validity of the antibody testing by experimenting with gluten withdrawal ahead of the testing, you are faced with two options: 1. Reintroduce significant amounts of gluten into your diet for a period of weeks, i.e., undertake a "gluten challenge". The most recent guidelines are the daily consumption of at least 10g of gluten (about the amount found in 4-6 slices of wheat-based bread) for at least two weeks leading up to the day of testing. Note: I would certainly give it more than two weeks to be sure. 2. Be willing to live with the ambiguity of not knowing whether gluten causes you problems because you have celiac disease or NCGS (Non Celiac Gluten Sensitivity). There is no test for NCGS. Celiac disease must first be ruled out and we have tests for it. Celiac disease has an autoimmune base. NCGS does not. GI symptoms overlap so without formal testing for celiac disease it can be very difficult to distinguish between the two in the early stages if it is celiac disease. Both conditions require elimination of gluten from the diet for symptom relief. Some experts feel that NCGS can be a precursor to celiac disease.
    • suek54
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      By suek54 · Posted

      Hi Kayla Huge sympathies. I was diagnosed in December, after 8 months of the most awful rash, literally top to toe. Mine is a work in progress. Im on just 50mg dapsone at the moment but probably need an increased dose to properly put the lid on it. As you have been now glutened, I wondered whether it might be worth asking for a skin biopsy to finally get a proper diagnosis? Sue  
    • MicG
      Test interpretations

      By MicG · Posted

      I had been eating reduced gluten until about 3 days before the test. I did realize that wasn’t ideal, but it was experimental to see if gluten was actually bothering me. One slip up with soy sauce and it was quite clear to me that it was, lol. 
    • trents
      Test interpretations

      By trents · Posted

      Possibly. Your total IGA (Immunoglobulin A, Qn, Serum) is actually high so you are not IGA deficient. In the absence of IGA deficiency, the most reliable celiac antibody test would be the t-Transglutaminase (tTG) IgA for which your score is within normal range. There are other things besides celiac disease that might cause an elevated DGP-IGA (Deamidated Gliadin Abs, lgA) for which you do have a positive score. It might also be of concern that your total IGA is elevated as that can indicate some other health problems, some of which are serious.  Had you been practicing a gluten free or a reduced gluten free diet prior to the blood draw? Talk to your physician about these things. I would also seek an endoscopy/biopsy of the small bowel to check for damage to the villous lining, which is the gold standard diagnostic test for celiac disease.
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