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

Biopsy After 3 Months Gluten Free?


Sarah1122

Recommended Posts

Sarah1122 Newbie

Hi all,

I am new to this site (and to Celiac in general) and first have to thank you all for the wonderful information and support I have found here. It really helps me feel not "so alone" during this difficult time.

On to my question: My blood work tested positive for Celiac in March - My GI wanted to do a biopsy to confirm, but my insurance company requries I pay a $500 deductable, which I could not afford at the time. My mom and sister both have celiac and now that I have been gluten free (mostly - there were a few accidents in the beginning) since April, I have no doubt that I have Celiac Disease.

However, in all my research, I found that the biopsy is the "gold standard" at confirming Celiac and have decided to have the test, both to rule out and/ or address other issues I am still having and to make it "official" in my medical record. I feel as though a specialist down the road may not take me seriously if I dont have the biopsy...

My question is - should I start to eat gluten again, as my test is in 2 weeks? I really do not want to - I am just finally starting to feel the slightest bit better and the thought of essentially poisoning myself for this test is upsetting. By the time I have the test, I will have been follow a gluten-free diet for 15 weeks, though I have been glutened a few times accidentally and gotten very sick (brain fog and depression are the worst!)

Will these gluten free weeks completely throw off the results? Or has this amount of time not allowed things to heal yet? (I was undiagnosed for almost 10 years, so I am thinking there must still be some damage there, right??)

What do you think? What has your experience been?

Any input is appreciated! Thank you!


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



Celiac.com Sponsor (A8-M):



Skylark Collaborator

Hi there and welcome.

All bets are off if you're gluten-free for that long before your biopsy. Eating gluten for two weeks after three months gluten-free is not likely to make a difference. I also completely agree about not poisoning yourself if your gluten symptoms are really bad.

With two first-degree relatives who are celiac and positive bloodwork I can't imagine a specialist wouldn't take you seriously. Did you come up positive for anti-endomysial? There are researchers saying people with anti-EMA maybe don't even need a biopsy because it's so specific for celiac disease.

ravenwoodglass Mentor

You have 2 first degree relatives with celiac and you have positive blood work. I would consider myself diagnosed if I were you. You would need to be back on gluten for about 3 months for the best chance at a positive biopsy and even then your results could be a false negative. You may also become even sicker from the challenge than you were before your blood tests and it could take longer for you to heal. IMHO you should simply skip the biopsy and save your money and health.

tarnalberry Community Regular

Ditto what everyone said - you need to be eating gluten at least three months prior to testing for a realistic expectation not to get a false positive.

Tina B Apprentice

Hi there and welcome.

All bets are off if you're gluten-free for that long before your biopsy. Eating gluten for two weeks after three months gluten-free is not likely to make a difference. I also completely agree about not poisoning yourself if your gluten symptoms are really bad.

With two first-degree relatives who are celiac and positive bloodwork I can't imagine a specialist wouldn't take you seriously. Did you come up positive for anti-endomysial? There are researchers saying people with anti-EMA maybe don't even need a biopsy because it's so specific for celiac disease.

I would just stick with the diet and forget the biopsy. What would it tell you that you don't already know. Of course the doc wants you to do it. he gets paid for it. You already know the bloodwork is positive and you have positive family members. By yourself a nice gift with the $500

Sarah1122 Newbie

Thank you all for your responses - and for confirming my feelings about starting to eat gluten now after so long without it. I just dont even think I could do it if I had to! Ugh! As much as I loved pizza before my diagnosis, if I was told I had to eat a slice right now, I would probably cry (or gag!) the whole way through it!

I am having a full physical tomorrow, running a bunch of tests to determine vitamin levels, anti-bodies, hormones, bone-density, and such, just to see where my health is right now. (many tests I learned about on this site, so again - thank you very much!) Going undiagnosed for about 12 years scares me... thinking of all the damage that could have been done. Doctors kept telling me I was "stressed" or "too young to be this tired, that it would pass." (I am 34 now) No one would listen! I had ultrasounds on my uterus because they thought the swelling was a tumor

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,037
    • Most Online (within 30 mins)
      7,748

    cbattiato
    Newest Member
    cbattiato
    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

    • Scott Adams
      This is an older article, but may be helpful.  
    • gfmom06
      I have had orthodontic work done. The 3M invisalign material was no problem. BUT my retainers are another matter. They seemed okay for a few months. Now, however, they cause a burning sensation on my tongue, gums and insides of my lips. The burning sensation is now spreading to my throat. I notice it when I breathe. This is annoying and interferes with my enjoyment of eating. I am visiting with my provider tomorrow. We'll see where this goes from here.
    • Beverage
      Exactly which blood tests were done? There are a few different ones and some docs don't do them all. Also, your results and reference ranges for each?
    • Jmartes71
      Thankyou so much for your words.Its a hard battle when a supposed well known hospital whose celiac " specialist " has down played me because my colon looks fine and put it in my medical and so pcp doesn't take seriously. In their eyes we all carry that gene.Im having alot of bad days trying to be positive because of it.
    • Scott Adams
      Your experience is both shocking and critically important for the community to hear, underscoring the terrifying reality that cross-contamination can extend into the most unexpected and invasive medical devices. It is absolutely devastating that you had to endure six months of sickness and ultimately sustain permanent vision loss because a doctor dismissed your legitimate, life-altering condition. Your relentless research and advocacy, from discovering the gluten in MMA acrylic to finding a compassionate prosthodontist, is a testament to your strength in a system that often fails celiac patients. While the scientific and medical consensus is that gluten cannot be absorbed through the skin or eyes (as the molecules are too large to pass through these barriers), your story highlights a terrifying gray area: what about a substance *permanently implanted inside the body*, where it could potentially shed microparticles or cause a localized immune reaction? Your powerful warning about acrylic lenses and the drastic difference with the silicone alternative is invaluable information. Thank you for sharing your harrowing journey and the specific, severe neurological symptoms you endure; it is a stark reminder that celiac is a systemic disease, and your advocacy is undoubtedly saving others from similar trauma.
×
×
  • 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.