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

Reliability Of Testing


susiek

Recommended Posts

susiek Apprentice

I read on another forum here that someone was saying that there are about 6 places in the US that can properly diagnose celiac disease through the blood test. I just had copious amounts of blood drawn and now am doubting I'll even get an accurate reading!

My lab didn't even know what vials to use...much less what the tests were for! lol

I'm getting bummed...

Of course it could be the 3 days without gluten. I'm in mourning!


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



Celiac.com Sponsor (A8-M):



par18 Apprentice
I read on another forum here that someone was saying that there are about 6 places in the US that can properly diagnose celiac disease through the blood test. I just had copious amounts of blood drawn and now am doubting I'll even get an accurate reading!

My lab didn't even know what vials to use...much less what the tests were for! lol

I'm getting bummed...

Of course it could be the 3 days without gluten. I'm in mourning!

Susie,

Did you try to get this test done on your own or were you referred to the lab by your doctor? I was Dx'd last May via biopsy and until a few days ago never had my blood tested for Celiac. My family doctor drew 2 samples and sent them to Labcor to analysis. He called me today and said the antibodies were ok but I did have one of the genetic markers. This did not surprise me as I know I have celiac disease. I was doing a follow-up after about a year on the gluten-free diet. I was pretty sure the anti-bodies were probably ok because I feel fine. My family doctor actually looked up the tests he wanted in a book to make sure the lab would test for the correct things. Have you been on the gluten-free diet? If so for how long?

Tom

susiek Apprentice

I had the labs done through my doctor. It was a hospital lab. My dictor seems pretty well-informed about celiac, but I was concerned about the lab once I read the other comment!

I went gluten-free on Friday after my doctor's visit and the blood draw. I was eating gluten prior to the test, pretty intensely for the past few weeks.

I took the list of 5 or 6 tests I have seen here referred to as the "celiac oanel." She was requesting 2 of these and when I showed her the list, she added the others.

She said that if the tests were inconclusive she would requset the biopsy, otherwise I would be getting a referral to a dietician. I'm unsure about the biopsy because I am now off gluten--I'm concerned that that wouldn't be accurate.

par18 Apprentice
I had the labs done through my doctor. It was a hospital lab. My dictor seems pretty well-informed about celiac, but I was concerned about the lab once I read the other comment!

I went gluten-free on Friday after my doctor's visit and the blood draw. I was eating gluten prior to the test, pretty intensely for the past few weeks.

I took the list of 5 or 6 tests I have seen here referred to as the "celiac oanel." She was requesting 2 of these and when I showed her the list, she added the others.

She said that if the tests were inconclusive she would requset the biopsy, otherwise I would be getting a referral to a dietician. I'm unsure about the biopsy because I am now off gluten--I'm concerned that that wouldn't be accurate.

How did you respond to the gluten-free diet and what types of symptoms did you have?

Tom

susiek Apprentice

Remember, I've only been gluten free since Mid Friday. I think Friday night was a wash because of all the blood they drew (they took 5 vials!) and a change in meds.

The biggest change is the absence of diarrhea. I was having D after most meals. I've had it twice since. Once because I think I got majorly glutened or at least cannot eat a pound of Italian sausage without repercussions--I ordered a gluten-free pizza and when it came realized it had a sausage "crust." It was nasty! But I ate it! I also had D today after eating taco meat on chips with some cheese--again, I think I just ate too much.

My symptoms were pretty typical of what I've read on the board. I got sick about 3 months ago. Was tested for e coli, salmonella, and parasites. Everything came back normal. Took some antibiotics and the cramping and major pain were gone, but the diarrhea stayed. Remembered about 2 weeks aho that my brother is gluten intolerant and started researching. Looking back I've had body aches and pains, foggy brain, dizziness, infertility (unexplored, just an inability to get pg in 8 years of trying), anemia.

When I saw my doc on Friday we started reviewing symptoms and realized that these have all been separate concerns through the years. I've seen the same doc for over 10 years. I've been xrayed for arthritis, tested for lupus/rheumatoid (which my sisters and mother have), questioned whether I was diabetic from the dizziness after eating (my blood sugars were actually low).

My doc said had she known about the gluten-intolerance sooner she would have requested the tests herself. I went in prepared to demand them, but she was cool and knowledgable!

par18 Apprentice
Remember, I've only been gluten free since Mid Friday. I think Friday night was a wash because of all the blood they drew (they took 5 vials!) and a change in meds.

The biggest change is the absence of diarrhea. I was having D after most meals. I've had it twice since. Once because I think I got majorly glutened or at least cannot eat a pound of Italian sausage without repercussions--I ordered a gluten-free pizza and when it came realized it had a sausage "crust." It was nasty! But I ate it! I also had D today after eating taco meat on chips with some cheese--again, I think I just ate too much.

My symptoms were pretty typical of what I've read on the board. I got sick about 3 months ago. Was tested for e coli, salmonella, and parasites. Everything came back normal. Took some antibiotics and the cramping and major pain were gone, but the diarrhea stayed. Remembered about 2 weeks aho that my brother is gluten intolerant and started researching. Looking back I've had body aches and pains, foggy brain, dizziness, infertility (unexplored, just an inability to get pg in 8 years of trying), anemia.

When I saw my doc on Friday we started reviewing symptoms and realized that these have all been separate concerns through the years. I've seen the same doc for over 10 years. I've been xrayed for arthritis, tested for lupus/rheumatoid (which my sisters and mother have), questioned whether I was diabetic from the dizziness after eating (my blood sugars were actually low).

My doc said had she known about the gluten-intolerance sooner she would have requested the tests herself. I went in prepared to demand them, but she was cool and knowledgable!

Susie,

I don't think I had anything like Italian sausage or taco meat for at least a couple on months into the gluten-free diet. I ate a lot of food early in the diet because I was so underweight. Most of it was naturally gluten free and only seasoned with salt and pepper. It would not really excite the taste buds but it was filling and I had no diarrhea after the second day on the diet. I think I ate my first meal in a resturant after almost 6 months. I eat out about once a week now. I have had no problems. I did not have any milk the first couple of weeks because I was not sure I could tolerate it but did eat sharp cheddar cheese right away. When I did introduce milk later it was ok. As far as I know I tolerate everthing except gluten. This includes nuts, shellfish, and soy among others. I don't know what you were used to eating before and how certain things may affect you now but I think I would try to keep it simple in the beginning and try to get as many symptom free days as you can and also try to keep a food log.

Tom

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,952
    • Most Online (within 30 mins)
      7,748

    SY8
    Newest Member
    SY8
    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

    • 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
    • DebJ14
×
×
  • 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.