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

What Is The Biopsy Like?


Woolygimp

Recommended Posts

Woolygimp Contributor

I just drove several hours to Houston to see a GI, and he did a liver panel and gave me a packet and said, "well maybe you should try a lactose free diet."

I even asked him to consider the possibility to Celiac, but he gave me the whole 'since your antibodies are negative, there's no possible way for you to have it' routine.

I am thinking about getting a biopsy when i go back, to know for sure. So I'm wondering what is the biopsy like? What is the name of it so I know exactly what to ask for? Is it painful? Are there any risks? Is it expensive?

I'm assuming that i need a GI to do it, but do I need a knowledgeable one to make sure he won't mis-interpret test results?


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



Celiac.com Sponsor (A8-M):



cyberprof Enthusiast

Hi Wooly,

My story is unusual, but here is my take on the biopsy for celiac. It's called an endoscopy and you can google it to get a definition. Basically, they give you a small sedative dose, then they spray the back of your throat with numbing spray and put a small tube down your throat. Takes all of 20 minutes. The tube has a camera in it and they can look for things like ulcers, cancer etc. They can also take 10-20 biopsies, which is what they can diagnose celiac with, among other things.

I thought I had an ulcer, had pain etc. Doc wanted me to have the endoscopy for that. They found no ulcer but took the biopsies anyway. Lucky for me, as it diagnosed celiac. My blood tests (subsequent after the endoscopy) were negative, so I would have gotten the same wrong-headed answer that you got.

I was lucky to be diagnosed so easily. I do have a lot of the symptoms, but I chalked them up to aging, not enough sleep, menopause, arthritis, depression etc., etc.

Maybe if you say "ulcer" you can get the endoscopy? A GI doc is the one you want to do it, because docs who do a procedure often are the best at it. Small (1 in a million) risk of perforation of stomach wall, reaction to anesthesia etc.... piece of cake. Cost is a lot, $1500 if not covered by insurance I think.

Going lactose free is an idea, you can always try it. And it won't mess up any celiac tests later.

Good luck to you. Being undiagnosed is hard, but going gluten free without a diagnosis has been done by many on this board with good results. It's free and requires no prescription.

I just drove several hours to Houston to see a GI, and he did a liver panel and gave me a packet and said, "well maybe you should try a lactose free diet."

I even asked him to consider the possibility to Celiac, but he gave me the whole 'since your antibodies are negative, there's no possible way for you to have it' routine.

I am thinking about getting a biopsy when i go back, to know for sure. So I'm wondering what is the biopsy like? What is the name of it so I know exactly what to ask for? Is it painful? Are there any risks? Is it expensive?

I'm assuming that i need a GI to do it, but do I need a knowledgeable one to make sure he won't mis-interpret test results?

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,035
    • Most Online (within 30 mins)
      7,748

    Cara Evans
    Newest Member
    Cara Evans
    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.