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

Post-diagnosis Tests


armarti2

Recommended Posts

armarti2 Newbie

I just had (MORE!) blood work done - testing fat-soluble vitamin absorption. They're also going to do a bone density scan - how is this done? Anything else I can expect? I thought I'd be done with the tests...

:blink:

Amy


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



Celiac.com Sponsor (A8-M):



Canadian Karen Community Regular

Hi Amy..... unfortunately, it is par for the course where celiac is concerned....

I just went to a celiac specialist this week, he also mentioned he is going to do a bone density test on my since I have had difficult to control celiac (he's not calling it refractory, yet....) for many, many years...... he said it is quite common for our bones to deteriorate due to our malabsorption.... he of course also did bloodwork too!!! I don't mind the tests though - I feel comforted in the fact that they are staying on top of it and not just ignoring this disease.....

Have a great day!

Karen

lovegrov Collaborator

Bone density is a painless procedure involving bone measruements by x-rays. I wouldn't think you'd be looking at more tests unless you don't improve. If they find some sort of major nutritional deficiencies they'll probably take more blood in a few months to see if that's improved.

richard

ryebaby0 Enthusiast

I'm with Karen; a doctor who wants more than a quick dx and dietary change knows what they are doing. Celiacs so often have profound nutrition issues when newly diagnosed, and they can be so easy to fix. My son took iron, zinc and folate for months, and it really helps him heal and feel better.

And refractory sprue, Karen? We saw a well-known GI at Johns Hopkins and it is her opinion (I'm paraphrasing, no lawsuits) and that of many "cutting edge" GI departments that there is no such thing. A celiac should get better (either clinically or pathologically) on a verified gluten-free diet. If you don't get better, there's more going on. Her thinking is the longer you've been sick, the longer it takes to truly recover, but long-term, the gluten-free diet should do it. Otherwise, you aren't really gluten-free, you have multiple allergies, multiple gi issues, or something. Have you contacted the Mayo Clinic? They do the most work studying "refractory" sprue and its solutions. I was amazed--they returned my emails!

joanna

Canadian Karen Community Regular

Hi Joanna.....

I would love for that to be the case (no such thing as refractory, that is....) as it would life a huge weight off my shoulders..... I think I will contact the Mayo (do they answer questions from someone outside the U.S., i.e. Canada?) I will wait though until after the colonoscopy and biopsies give us more answers that we are looking for and what we are dealing with..... I should hear within the next few days when the colonoscopy is scheduled for.....

But if it is the case where the longer you have had celiac, the longer it takes to heal, that would make sense in my case. I have had bowel problems starting as a child, anemic my whole life, diagnosed for the first time as celiac in my early 20's.... after a year on the diet with no change, he changed his diagnoses to Crohn's disease.... that is until 1 1/2 years ago when the blood test and biopsy confirmed celiac for sure.... so it really has only been 1 1/2 years gluten-free (with some inadvertent slips....). I am 41 years old now, so that is A LOT of years of damage done..... Maybe there is hope for me to see improvement yet!!!!

Karen

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,605
    • Most Online (within 30 mins)
      7,748

    LWceliac38
    Newest Member
    LWceliac38
    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

    • Scott Adams
      It seems like you have two choices--do a proper gluten challenge and get re-tested, or just go gluten-free because you already know that it is gluten that is causing your symptoms. In order to screen someone for celiac disease they need to be eating gluten daily, a lot of it--they usually recommend at least 2 slices of wheat bread daily for 6-8 weeks before a blood screening, and at least 2 weeks before an endoscopy (a colonoscopy is no used to diagnose celiac disease). Normally the blood panel is your first step, and if you have ANY positive results there for celiac disease the next step would be to take biopsies of your villi via an endoscopy given by a gastroenterologist.  More info on the blood tests and the gluten challenge beforehand is below: The article includes the "Mayo Clinic Protocol," which is the best overall protocol for results to be ~98% accurate. Here is more info about how to do a gluten challenge for a celiac disease blood panel, or for an endoscopy: and this recent study recommends 4-6 slices of wheat bread per day:   Not to discourage you from a formal diagnosis, but once you are diagnosed it may lead to higher life and medical insurance rates (things will be changing quickly in the USA with the ACA starting in 2026), as well as the need to disclose it on job applications. While I do think it's best to know for sure--especially because all of your first degree relatives should also get screened for it--I also want to disclose some negative possibilities around a formal diagnosis that you may want to also consider.  
    • Wheatwacked
      Yes.  Now, if you hit your finger with a hammer once, wouldn't you do your best not to do it again?  You have identified a direct connection between gluten and pain.  Gluten is your hammer.  Now you have to decide if you need a medical diagnosis.  Some countries have aid benefits tgat you can get if you have the diagnosis, but you must continue eating a gluten-normal diet while pursuing the diagnosis. Otherwise the only reason to continue eating gluten is social. There are over 200 symptoms that could be a result of celiac disease.. Celiac Disease and Non Celiac Gluten Sensitivity  both cause multiple vitamin and mineral deficiency.  Dealing with that should help your recovery, even while eating gluten.  Phosphatidyl Choline supplements can help your gut if digesting fats is a problem,  Consider that any medications you take could be causing some of the symptoms, aside from gluten.        
    • trents
      Welcome to the forum, @Ben98! If you have been consciously or unconsciously avoiding gluten because of the discomfort it produces then it is likely that your blood antibody testing for celiac disease has been rendered invalid. Valid testing requires regular consumption of generous amounts of gluten. The other strong possibility is that you have NCGS (Non Celiac Gluten Sensitivity) which shares many of the same symptoms with celiac disease but does not have the autoimmune component and thus does not damage the small bowel lining. It is 10x mor common than celiac disease. There is currently no test for NCGS. Celiac disease must first be ruled out. Some experts in the field believe it can be a precursor to the development of celiac disease. Having one or both of the primary genes for developing celiac disease does not imply that you will develop active celiac disease. It simply establishes the potential for it. About 40% of the population has the genetic potential but only about 1% develop active celiac disease. 
    • Ben98
      TTG blood test and total IGA tested on many occasions which have always remained normal, upper GI pain under my ribs since 2022. I had an endoscopy in 2023 which showed moderate gastritis. no biopsy’s were taken unfortunately. genetic test was positive for HLADQ2. extreme bloating after eating gluten, it’ll feel like I’ve got bricks in my stomach so uncomfortably full. the pain is like a dull ache under the upper left almost like a stitch feeling after a long walk. I am just wanting some advice has anyone here experienced gastritis with a gluten issue before? thank you  
    • Wheatwacked
      "Conclusions: The urinary iodine level was significantly lower in women with postmenopausal osteoporosis, and iodine replacement may be important in preventing osteoporosis"  Body iodine status in women with postmenopausal osteoporosis Low iodine can cause thyroid problems, but Iodine deficiency will not show up in thyroid tests.  Iodine is important for healing, its job is to kill off defective and aging cells (Apoptosis). Skin, brain fog, nails, muscle tone all inproved when I started taking 600 mcg (RDA 150 - 1000 mcg) of Liquid Iodine drops. Some with dermatitis herpetiformis, Iodine exacerbates the rash.  I started at 1 drop (50 mcg) and worked up to 12 drops, but I don't have dermatitis herpetiformis.
×
×
  • 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.