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
      131,630
    • Most Online (within 30 mins)
      7,748

    Emma Gallagher
    Newest Member
    Emma Gallagher
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Wheatwacked
      Gluten free food is not fortified with vitamins and minerals as regular food is.  Vitamin deficiencies are common especially in recently diagnosed persons,  Get a 25(OH)Vitamin D blood test. And work on raising it.  The safe upper blood level is around 200 nmol/L.    "Low serum levels of 25(OH)D have been associated with increased risk of autoimmune disease onset and/or high disease activity. The role of vitamin D in autoimmune diseases   🏋️‍♂️Good job!   I find the commercial milk will give me mild stomach burn at night, while pasture/grassfed only milk does not bother me at all.  While you are healing, listen to your body.  If it hurts to eat something, eat something else.  You may be able to eat it later, or maybe it is just not good for you.  Lower your Omega 6 to 3 ratio of what you eat.  Most omega 6 fatty acids are inflammation causing.    The standard american diet omega 6:3 ratio is estimated at upward of 14:1.  Thats why fish oil works
    • Inkie
      I  notice a reaction to tea bags, possibly due to gluten or other substances. Is this recognizable?
    • trents
      The blood tests you had done are not the main ones. The two main ones are the "Total IGA" (to check for IGA deficiency) and the "TTG-IGA". Current guidelines for the "gluten challenge" when people have been gluten free for a significant time period are the daily consumption of at least10g of gluten (about the amount in 4-6 slices of wheat bread) for at least two weeks leading up to the day of the blood draw. That should give you some perspective.
    • Xravith
      Thank you, really.  I took a test for DGP-IgA and DGP-IgG. Effectively, it is not enough to discard Celiac Disease. I was consuming gluten until then, I only started gluten-free some days ago, when the symptoms became horrible and now I feel considerably better, which is a second confirmation that gluten is the main problem. It's been more than 4 years I have the same suspect, when I first thought gluten was causing me problems, I made a gluten-free diet for a year, I felt really good as never before. However, neither I or my parents were well informed about Celiac disease, so none of us tried to make further exams. My father suffer digestive problems and other members of my family as well. Unfortunately, no one have ever been tested for Celiac disease. I'll have to restart eating gluten in the next weeks, so I can make a serious blood test in laboratory, hopefully between two or three months.
    • trents
      As Scott said, in order for celiac disease testing to be valid, you need to be eating generous amounts of gluten on a regular basis for weeks or months before the blood draw. The blood tests are designed to detect antibodies that the immune system produces in response to the ingestion of gluten. It takes time for them to build up in the blood to detectable levels.
×
×
  • 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.