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

Not Yet Diagnosed


Findabhair

Recommended Posts

Findabhair Newbie

I have been seeing a psychiatrist for almost three-years now, and she just got blood work results back, and after examining that, as well as my past health issues, as well as looking into my family heritage. As well as the recent drastic change in my thyroid levels. And has suggested that I see a family doctor to be checked to see if I am Celiac.

I have been through a lot of health issues both mentally and physically through my life. And honestly this terrifies me.

I have no idea what to expect. I am absolutely terrified. I have no idea what to expect for the testing or anything. And as far as I know, none of my friends or family suffer from this.

Can anyone help me understand what will happen from here?

What can I expect to be included in the tests. And after?


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



Celiac.com Sponsor (A8-M):



mushroom Proficient

Hello and welcome. I hope you find this board a place of comfort and support.

There is really nothing to be of afraid of with celiac testing or diagnosis. And if you test positive you will find it very comforting to have an explanation for a lot of symptoms that may have been puzzling you.

The first line of testing for celiac disease is a panel of blood tests, to test for antibodies to gliadin which is a protein in wheat., rye and barley. There are several different kinds of tests they run so they will probably take at least three different vials of blood. If these tests come out positive, you will probably be referred to a gastroenterologist who will perform what is called an endoscopy where they insert a small tube with a camera on it into your stomach, and take some tissue samples from the upper part of your small intestine, to see if there has been any damage done there by gluten. These are then put onto slides and read by a pathologist because often the damage cannot be seen with the naked eye, although the doctor may be able to see it through the scope.. The procedure itself is pretty routine and while it may sound frightening it is a very low risk procedure and you will remember none of it. They do not give you anesthesia, but they give you a sedative, and another drug which makes you not remember anything that happens. The first thing you know you will be asking when are they going to do it, and they will tell you they already have done it :) You will recover from it very quickly, not like from an anesthetic, but you will need someone to drive you home.

If the tests are positive you will be instructed to eat a diet that is free of wheat, rye and barley; that is, a gluten free diet. And while this does take a little bit of adjusting to, because after all we have all been eating gluten all our lives, once you get the hang of it and once you see the benefit of it, it is very easy to follow.

If you have to be diagnosed with something, celiac is one of the best diagnoses to have because there is no medication to take for it, no surgery required; you just have to change what you eat. And while we can be fearful of change, there is no reason to be terrified of this, I can assure you.

Since celiac is a genetically based disease, if that is in fact what you have you will have received a celiac gene from at least one of your parents; but not everyone with the gene develops the disease - there seems to need to be a triggering event, an emotional of physical trauma, that sets the process in motion. This trigger is not yet fully understood.

Please feel free to ask whatever questions and concerns you have and the good folks here will be glad to help you. :)

Marz Enthusiast

Nice reply mushroom, I think it's all covered really :)

Welcome to the forum, and don't be scared - you've got a lot to look forward to if Celiac disease is your problem, including potentially decreasing/disappearing psychiatric problems. See Skylark's posts for how her bipolar condition got better, lots of us suffered from panic attacks/anxiety that disappeared going gluten-free.

Edit: Apparently I've got lots more to say :D

Just wanted to say you've got a fantastic psychiatrist there. I struggled to get my *Gastroenterologist* to check me for Celiac disease, so to have a Psychiatrist be aware of the neurological connection and get blood tests done is excellent.

Sadly your family doctor may not be informed about what tests to run. You need to get the full celiac panel done (and if they don't have anything like that, specify IgA and IgG anti-gliadin, tTG, and IgA total blood tests. There's also a new anti-deaminated gliadin test that's even better than the tTG. The total IgA is to test for IgA deficiency which is more common among celiacs. It's *not* IgE tests - that's an allergy, and completely unrelated to celiac disease.

Even with negative blood tests, you could have intestinal damage - your doctor should refer you to a specialist to have an endoscopy done with biopsies, to check for small intestine damage.

And even if both of those are *negative*, there's still a chance you could be sensitive to gluten. Especially with neurological problems (Which may involve a slightly different form of the tTG antibody), you could have negative tests, and find a lot of relief from random problems going gluten free.

But get the tests done first before you go gluten-free, and then ask your doctor/therapist about whether you should try the diet and see if it helps.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

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

    AnnaLousGFBakery
    Newest Member
    AnnaLousGFBakery
    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.