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

Question About Results


huenix

Recommended Posts

huenix Newbie

I hesitate to even post this because I am sure the "correct" answer is talk to my GI, but...

Two years ago I was diagnosed with GERD. Last fall, I got giardiasis from contaminated water, and after about 6 weeks of suffering finally got a positive result in testing. My regular doc (actually his PA) gave me Flagyl, and the giardiasis cleared up. In the followup appointment, the PA found occult blood in my stool, and did bloodwork.

My liver function tests were a bit high (140s for AST and ALT) and my total bili was high (I have Gilberts, or at least thats what I have been told for a couple years...) I was also mildly anemic. PA requested that I see the gastro, which I did. Gastro repeated blood tests (6 weeks or so later..) and did a RUQ sono of the liver.

Repeat bloodwork was mostly perfectly normal. Total bili was still high (1.2) and the gastro had screenings done for Hep, Celiac and some other stuff. Everything was negative except:

tTG-IgA was 14, with >8 as positive

The other AGA test was right dead in the middle of maybe. I don't have the sheet here with me so while I remember the result was inconclusive, I don't remember the range.

Last but not least, I am still anemic, even talking an iron supplement and dietary changes to increase iron consumption.

RUQ sono came back as perfectly normal.

Last week I had an Endo and Colonoscopy per the gastro. Everything was fine as far as it went with mild gastro irritation (even on Prilosec...) The biopsy report says"No flattening of the villi is observed. There is, however, a slight increase in the number of plasma cells in the core of the villi and a slight increase in the number of lymphocytes in the epithelium..." It mentions that if clinically suspected, this could represent a mild form of celiac disease and recommends seriologic testing and clinical pathological correlation.

I've had gastro discomfort for a long time and always wrote it off as GERD, Frequent mild diarrhea. Very occasional nausea.

Last but not least I should at least mention that I am somewhat of a distance runner, and I'm in overall good shape (barring the last few months due to the giardia...)

Any thoughts? Anything I should specifically talk with the GI about?

Thanks!


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



Celiac.com Sponsor (A8-M):



Luvbeingamommy Contributor

Your story sounds similiar to mine and I don't see my GI doc for another two weeks.

I've also had high bilirubin, although usually around 1.2, not real high. I had some liver enzyme problems as well. My sypmtoms are stomach pain, nausea (bad sometimes), on and off diarrhea. Also had a stroke, and am a very healthy 25 year old. I just decided to give the diet a try, only on day 2 though. So while I can't offer any advice, just wanted to let you know you are not alone.

ravenwoodglass Mentor

I would start the diet. You have had a positive blood test and a endo that showed that you may be (probably are with the positive blood work) in the early stages of celiac. I would start the diet. That is the truest test. It is very common for us to have elevated liver panels, GERD and the other symptoms you are having. If you have any questions please feel free to ask and read as much as you can here.

nora-n Rookie

This biopsy finding is typical for early celiac, and the ttg test is quite specific for celiac, but may be positive in giardiasis.

But by the time it was done, it should probably have gone down.

to read more about the significance of the biopsy findings, go to Dr. Lewey's blog somewhere on his site, www.thefooddoc.com .

huenix Newbie

Crap. Reading all the giardia/celiac disease links just gets more confusing. I agree with you that it -should- have gone away and I certainly have had zero giardia-specific symptoms since finishing the run of Flagyl.

Whats stressing me out about all this is that I don't want this to end with "Well, we don't know what's wrong with you." Especially since, in 9 days since starting the gluten-free diet, I have not had any anxiety issues whatsoever, a decrease in stomach pains, and I've been sleeping a lot better. I don't want that to be psychosomatic.

ravenwoodglass Mentor

Especially since, in 9 days since starting the gluten-free diet, I have not had any anxiety issues whatsoever, a decrease in stomach pains, and I've been sleeping a lot better.

I don't want that to be psychosomatic.

It's not. Please do stick with the diet, it does sound like it is helping.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,945
    • Most Online (within 30 mins)
      7,748

    Miyasato
    Newest Member
    Miyasato
    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.