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

Which Lab Is Best For Testing


dog lover

Recommended Posts

dog lover Newbie

HI, I need to get tested and was looking at enterolab.

What is everyone's opinion of this lab and do you have

suggestions of other labs that are reliable? Thanks, a newbee.

:D


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



Celiac.com Sponsor (A8-M):



Guest greengirl
HI, I need to get tested and was looking at enterolab.

What is everyone's opinion of this lab and do you have

suggestions of other labs that are reliable? Thanks, a newbee.

:D

My experience with Enterolab has been great. I know that Dr. Fine gives lectures around the country and also runs a nonprofit Intestinal Health Institute. He has lots of information posted on his website about gluten intolerance, celiac, and the genes that predispose to this condition. Someone else posted that he is sponsoring a gluten free camp this summer and will give nightly lectures at the 4 day event. When I called there for help getting the insurance to cover my tests, they were more than willing to help. (This is still in the works with BCBS but if I can manage to get it covered as an in-network expense, then I think anyone else with BCBS would be able to as well. I'll let you know...). Once you've gotten your results the staff is available for any questions and I know that at least several people on this board have gotten replies from Dr. Fine addressing their individual concerns.

I truly believe that this will be the "gold standard" for diagnosing celiac/gluten intolerance in the future. I had negative results with bloodwork, biopsy, and had many, many lab tests that were inconclusive. Enterolab confirmed what I suspected all along. For my daughter, I skipped all the labwork and went right to enterolab. She had extremely high numbers in every category. We have both had success with the gluten-free diet, and in her case, Gluten-free Casein-free diet, but we did want a diagnosis to be sure. Incidentally, my Gastro specialist accepted the enterolab results as legitimate.

If you can afford the celiac panel I would do that, rather than just the IgA test. In my daughter's case it showed us the severity of her malabsorption and we found out she was casein intolerant. We also found out that she has 2 copies of the gi/celiac genes, which puts her sisters at an even higher risk (we had no idea my husband was passing down a gene, as well!)

Good luck!

Christine

CarlaB Enthusiast

I also did the full panel, but did not do the genetic part on my kids. One daughter and I came out positive, the other daughter negative. I, too, was very happy with everything about my experience working with them. My primary care doc accepted the testing. I didn't bother working with my GI doc when he was totally discounting my dietary response after all my tests came back negative, I can only assume what he would have thought of the results.

The thing I like about Enterolab is that you can catch it before it gets so bad that you have damage to your intestines and more autoimmune diseases. My daughter's absorption was great. Mine was borderline, and I took it after three months gluten-free (and things had changed dramatically!!). I can't imagine how sick I would have been if I had waited for the current "gold standard" of a positive biopsy!! This is why so many celiacs are so sick for so long before being diagnosed!

I don't know of other labs like them, so I can't recommend anyone else.

AndreaB Contributor

I just had my whole family, except the baby, tested by Enterolab. The results came back quickly and before I placed my order Phyllis was very helpful. Haven't talked to anyone else over there. My doctor was willing to run a celiac panel for me but I had been gluten free (or mostly) for 1 1/2 months. Right now my son is my barometer on whether I've eaten something bad. He's pretty sensitive.

dog lover Newbie

THANKS TO ALL FOR RESPONDING, I REALLY APPRECIATE IT,

AS YOU ALL KNOW THIS ISN'T A PICNIC. I'LL LET YOU

KNOW RESULTS AFTER I GET ALL THIS ORDERED AND SENT BACK.

THANKS AGAIN

Archived

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

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      132,918
    • Most Online (within 30 mins)
      7,748

    Dizzyma
    Newest Member
    Dizzyma
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • xxnonamexx
      very interesting thanks for the info  
    • Florence Lillian
      More cookie recipes ...thanks so much for the heads-up Scott.  One can never have too many.  Cheers, Florence.
    • Russ H
      Hi Charlie, You sound like you have been having a rough time of it. Coeliac disease can cause a multitude of skin, mouth and throat problems. Mouth ulcers and enamel defects are well known but other oral conditions are also more common in people with coeliac disease: burning tongue, inflamed and swollen tongue, difficulty swallowing, redness and crusting in the mouth corners, and dry mouth to name but some. The link below is for paediatric dentistry but it applies to adults too.  Have you had follow up for you coeliac disease to check that your anti-tTG2 antibodies levels have come down? Are you certain that you not being exposed to significant amounts of gluten? Are you taking a PPI for your Barrett's oesophagus? Signs of changes to the tongue can be caused by nutritional deficiencies, particularly iron, B12 and B9 (folate) deficiency. I would make sure to take a good quality multivitamin every day and make sure to take it with vitamin C containing food - orange juice, broccoli, cabbage etc.  Sebaceous hyperplasia is common in older men and I can't find a link to coeliac disease.   Russ.   Oral Manifestations in Pediatric Patients with Coeliac Disease – A Review Article
    • cristiana
      Hi @Charlie1946 You are very welcome.   I agree wholeheartedly with @knitty kitty:  "I wish doctors would check for nutritional deficiencies and gastrointestinal issues before prescribing antidepressants." I had a type of tingling/sometimes pain in my cheek about 2 years after my diagnosis.  I noticed it after standing in cold wind, affecting  me after the event - for example, the evening after standing outside, I would feel either tingling or stabbing pain in my cheek.   I found using a neck roll seemed to help, reducing caffeine, making sure I was well-hydrated, taking B12 and C vitamins and magnesium.  Then when the lockdowns came and I was using a facemask I realised that this pain was almost entirely eliminated by keeping the wind off my face.  I think looking back I was suffering from a type of nerve pain/damage.  At the time read that coeliacs can suffer from nerve damage caused by nutritional deficiencies and inflammation, and there was hope that as bodywide healing took place, following the adoption of a strict gluten free diet and addressing nutritional deficiencies, recovery was possible.   During this time, I used to spend a lot of time outdoors with my then young children, who would be playing in the park, and I'd be sheltering my face with an upturned coat collar, trying to stay our of the cold wind!  It was during this time a number of people with a condition called Trigeminal Neuralgia came up to me and introduced themselves, which looking back was nothing short of miraculous as I live in a pretty sparsely populated rural community and it is quite a rare condition.   I met a number of non-coeliacs who had suffered with this issue  and all bar one found relief in taking medication like amitriptyline which are type of tricyclic anti-depressant.   They were not depressed, here their doctors had prescribed the drugs as pain killers to address nerve pain, hence I mention here.  Nerve pain caused by shingles is often treated with this type of medication in the UK too, so it is definitely worth bearing in mind if standard pain killers like aspirin aren't working. PS  How to make a neck roll with a towel: https://www.painreliefwellness.com.au/2017/10/18/cervical-neck-roll/#:~:text=1.,Very simple. 
    • Scott Adams
      We just added a ton of new recipes here: https://www.celiac.com/celiac-disease/gluten-free-recipes/gluten-free-dessert-recipes-pastries-cakes-cookies-etc/gluten-free-cookie-recipes/
×
×
  • 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.