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

Testing Question


AliB

Recommended Posts

AliB Enthusiast

My blood test came back negative.

Over here in the UK its like getting blood out of a stone. I even rang the Lab to ask if they could interpret for me as my doctor said he didn't know enough about it, but they said they couldn't help as it is illegal! Can you believe that?

Anyway, I did manage at least to get the doc's receptionist to give me what did come back - the following

tTG 1uml range 0 - 10

IgA 1.54 range .85 - 4.68

Doesn't seem like nearly enough testing or information to me. Any other opinions?

Other than putting me forward for gastroscopy which wouldn't show now as I am gluten-free with no intention of going back to it, I'm pretty stuffed really.

Shame I don't live in the States, I'd probably be better off getting a stool test done with Enterolab.


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



Celiac.com Sponsor (A8-M):



nikki-uk Enthusiast
tTG 1uml range 0 - 10

IgA 1.54 range .85 - 4.68

Doesn't seem like nearly enough testing or information to me. Any other opinions?

Looks like your tTg was NEG (usually anything over 10 is POS)

Also your total IgA count looks normal (Low IgA negates the tTg test)

There were a few other bloods your GP could have done (Haemoglobin, EMA etc) but the tTG is generally thought to be the most important.

Were you eating gluten when you had the bloods?...although NEG bloods doesn't mean you DON'T have celiac disease

As you say - if you are already gluten-free there's not much point in having any biopsies - do you feel any better for going gluten-free??? :)

Ursa Major Collaborator

You absolutely CAN do the enterolab tests, if you can afford to pay for overnight courier to ship the samples back to them. They will send their kit all over the world, and give you the results by e-mail.

AliB Enthusiast

I was eating gluten and dairy until I had the blood taken then started immediately after. I noticed that sometimes if the IgA reading are low it can be because the antibody levels are low for some reason so then a test has to be done to measure those.

Having read the info, it seems that the Enterolab stool tests may be far more accurate. As it said, there are far more likely to be antibodies in the stool than in the blood.

Unfortunately we don't have health insurance here to pay for it, we have the good old NHS and are at the mercy of it so we don't have the choice (despite the fact that we actually pay for it via taxes!), and I just don't happen to have a spare $400 dollars floating around.........

How many had positive results from the Enterolab tests after getting negs on blood and/or biopsy? Was your insurance happy to pay? Did your doctor accept the test as positive enough for a diagnosis? A stool test has got to be cheaper than a biopsy at the end of the day and the NHS likes the word 'cheap'!

AliB Enthusiast

Sorry Nikki, I forgot to answer your other question - yes I do feel a lot better.

I started on Monday 28th Jan as I couldn't cope with the pain and relentless diarrhoea any more.

Within 6 hours the terrible pain in my stomach had gone and the diarrhoea had stopped.

Within 5 days I was beginning to gain more energy.

Within a week the bloating had stopped and my stomach had calmed right down and is coping well apart from the odd reaction (gippy stomach and horrible backache) when I eat something it doesn't like (I'm still trying to pinpoint the culprits!)

Within 2 weeks I was able to digest meat again. I have also been sleeping much sounder and am far less restless. It looks like, for the first time in my life, I might actually find sleep to be refreshing - I am so looking forward to bouncing out of bed in the morning rather than dragging myself out feeling hungover (I wouldn't mind, but I can't even drink alcohol as it makes me cough!)

The restless legs have stopped, although still a little stiff the pain in my shoulder has gone, the pain in my coccyx is much improved. The big black rings under my eyes that have been a permanent fixture for the last 35 years are finally starting to fade (don't think I'll be quite so successful with the bags though!)

Although I had a background headache for the last week that has been a lot better today. I am very tired, but I have missed a lot of sleep over the last few months and undoubtedly, along with the withdrawal and detox effects, my body has a lot of catching up to do.

I am not that worried about a diagnosis, but being able to get some products on the NHS would be handy as they aren't particularly cheap (we do get free Scripts here in Wales!).

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Scott Adams replied to Jhona's topic in Introduce Yourself / Share Stuff
      35

      Does anyone here also have Afib

    2. - Jacki Espo replied to CDFAMILY's topic in Related Issues & Disorders
      5

      Covid caused reoccurrence of DH without eating gluten

    3. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      1

      New Celiac Mama in My 30s

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

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,955
    • Most Online (within 30 mins)
      7,748

    Mabelie
    Newest Member
    Mabelie
    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

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • 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.