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

Help - Need Info Quick


Jalar

Recommended Posts

Jalar Newbie

I am having an upper GI with a biopsy on Monday, Feb 26th :blink: . I had a gastric ulcer last year and for the past six months have been having nausea, constipation, pasty stool, gas, cramping and so forth. When it came up that I was having this 2nd upper endoscopy my mom mentioned that several people in my family have Celiac's (many more have irritable bowel). What do I need to do to make SURE that they doctors check for gluten intolerance. What do I need to know for Monday? I hate to miss this opportunity because I have SO little time for research. Can you help me??? :unsure: Thank you ! Thank you!


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



Celiac.com Sponsor (A8-M):



CarlaB Enthusiast

They need to take several biopsies -- 7-10 -- to see if you have villi damage. As long as they're in there, they may as well do the biopsies. I'd insist on it!!

chocolatelover Contributor

Absolutely make sure they do multiple biopsies from multiple spots. I had an endoscopy that was a complete waste of time because they only took one biopsy because "everything looked normal". Unless the damage is significant, they won't be able to see anything with the scope. Usually they find the damage when looking microscopically at the biopsies.

Also make sure that they know that you have a family history of celiac disease.

Good luck!

sherylj Rookie
I am having an upper GI with a biopsy on Monday, Feb 26th :blink: . I had a gastric ulcer last year and for the past six months have been having nausea, constipation, pasty stool, gas, cramping and so forth. When it came up that I was having this 2nd upper endoscopy my mom mentioned that several people in my family have Celiac's (many more have irritable bowel). What do I need to do to make SURE that they doctors check for gluten intolerance. What do I need to know for Monday? I hate to miss this opportunity because I have SO little time for research. Can you help me??? :unsure: Thank you ! Thank you!

Just had my biopsy done a month ago,,it was easy, cause they sedated me completely. I highly recommend complete sedation,,not just numbing the throat as some folks have reported.

And yes serveral biopsies of the villi(lining of the small intestine). My report states the biopsies came from the second a part of the duodenum?? I guess there are diffeent parts to the small intestine?? Can someone answer that question

?

Your symptoms sound so close to mine,,the nausea,,vomiting, constipation, excess gas and belching. I just joined the forum yesterday and finding a wealth of experiences to draw on. It always helps to talk to someone who has been THERE.

Good luck!!

sherylj Rookie
Absolutely make sure they do multiple biopsies from multiple spots. I had an endoscopy that was a complete waste of time because they only took one biopsy because "everything looked normal". Unless the damage is significant, they won't be able to see anything with the scope. Usually they find the damage when looking microscopically at the biopsies.

Also make sure that they know that you have a family history of celiac disease.

Good luck!

I came away from my biopsy thinking I didn't have celiac because it wasn't apparent from dr. initial internal scope exam. The microscopic exams of biopsies were the key. The dr. told my husband it didn't look like celiac (while I was still sedated) and I went home and ate gluten for a week until dr. called and said,,,oh, by the way, the biopsies show celiac.

Maybe the reason my villi looked "normal" UNTIL UNDER THE MICROPSCOPE is because I have off and on followed a gluten-free diet for 10 years...I ate gluten foods the week before the test and had prob not caused enough damage for the naked eye to see. My symptoms however had gotten so bad prior to the testing I was off and on the gluten-free diet. It seems I can eat about a week worth of 1 gluten a day and then "TILT" the bad symtoms start and I have a painful night. So then I would go gluten-free for a week or so and start the whole cycle of "cheating" again. Now that I have a definite diagnosis and am no longer self diagnosed I am going to dedicate myself to totally gluten free to try and lift my depression and see if I can l live life with joy and happiness instead of anxiety/depression.

Hope you find a definite diagnosis cause it really does change your outlook on life when you feel you have the power and choices to change how you feel!! Sherylj

mamabear Explorer
I am having an upper GI with a biopsy on Monday, Feb 26th :blink: . I had a gastric ulcer last year and for the past six months have been having nausea, constipation, pasty stool, gas, cramping and so forth. When it came up that I was having this 2nd upper endoscopy my mom mentioned that several people in my family have Celiac's (many more have irritable bowel). What do I need to do to make SURE that they doctors check for gluten intolerance. What do I need to know for Monday? I hate to miss this opportunity because I have SO little time for research. Can you help me??? :unsure: Thank you ! Thank you!

Everyone has given you great advice. The standard for biopsy is in the second portion of the duodenum which is the first 1/3 if the small intestine. 6 biopsies should be made. It is absolutely important that the doc is made aware of your family history of celiac. If you can, find out who in your family had celiac as well as IBS and any other GI related illness;and I suggest writing all that down to give to the doctor. Hopefully you'll have an answer by this time next week. Be assertive and request that the biopsies be done.

Let us know how it goes.

happygirl Collaborator

Discuss with your GI before the procedure that you want "multiple biopsies, in multiple locations" to check for Celiac damage, even if it doesn't look like damage while he is in there. Tell him regardless of what it looks like, you want the full biopsies taken, because you don't want to have to go through this again. Best of luck.


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



Celiac.com Sponsor (A8-M):



mamabear Explorer
Just had my biopsy done a month ago,,it was easy, cause they sedated me completely. I highly recommend complete sedation,,not just numbing the throat as some folks have reported.

And yes serveral biopsies of the villi(lining of the small intestine). My report states the biopsies came from the second a part of the duodenum?? I guess there are diffeent parts to the small intestine?? Can someone answer that question

?

Your symptoms sound so close to mine,,the nausea,,vomiting, constipation, excess gas and belching. I just joined the forum yesterday and finding a wealth of experiences to draw on. It always helps to talk to someone who has been THERE.

Good luck!!

The small intestine has 3 parts....first after the stomach is the duodenum, The second part is the jejunum and the third part is the ileum which adjoins the large intestine or colon.

babygirl1234 Rookie

my GI doctor did both scops and did the biopscys on both, so the GI doctor i have is a good doctor and supper nice

Jalar Newbie

I am home from my upper GI. Good news - my ulcer is gone. :P Bad news - Dr. said my stomach and intestinal track look irriated and inflammed. :( I asked for several biopsies to be taken and mentioned my family history of Celiacs. The doctor agreed and said she would send the biopsy off and we would know something in about a week. Soooo..... I go back to see her in an office setting in a week or two.

Thanks everyone for your help! ;) I will keep you posted!

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Flash1970 replied to Ginger38's topic in Related Issues & Disorders
      7

      Shingles - Could It Be Related to Gluten/ Celiac

    2. - trents replied to Roses8721's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      10

      GI DX celiac despite neg serology and no biopsy

    3. - Roses8721 replied to Roses8721's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      10

      GI DX celiac despite neg serology and no biopsy

    4. - Ginger38 replied to Ginger38's topic in Related Issues & Disorders
      7

      Shingles - Could It Be Related to Gluten/ Celiac

    5. - Scott Adams replied to Silk tha Shocker's topic in Gluten-Free Foods, Products, Shopping & Medications
      1

      Help


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,483
    • Most Online (within 30 mins)
      7,748

    AML2013
    Newest Member
    AML2013
    Joined

  • Celiac.com Sponsor (A20):



  • Celiac.com Sponsor (A22):




  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A21):


  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • Flash1970
      You might try Heallix.  It's a silver solution with fulvic acid. I just put the solution on with a cotton ball.  It seemed to stop the nerve pain. Again,  not in your eyes or ears.   Go to heallix.com to read more about it and decide for yourself Also,  I do think nerve and celiac combined have a lot to do with your susceptibility to shingles breaking out. 
    • trents
      Celiac disease requires both genetic potential and a triggering stress event to activate the genes. Otherwise it remains dormant and only a potential problem. So having the genetic potential is not deterministic for celiac disease. Many more people have the genes than actually develop the disease. But if you don't have the genes, the symptoms are likely being caused by something else.
    • Roses8721
      Yes, i pulled raw ancetry data and saw i have 2/3 markers for DQ2.2 but have heard from friends in genetics that this raw data can be wildly innacurate
    • Ginger38
      Thanks, I’m still dealing with the pain and tingling and itching and feeling like bugs or something crawling around on my face and scalp. It’s been a miserable experience. I saw my eye doc last week, the eye itself was okay, so they didn’t do anything. I did take a 7 day course of an antiviral. I’m hoping for a turnaround soon! My life is full of stress but I have been on / off the gluten free diet for the last year , after being talked into going back on gluten to have a biopsy, that looked okay. But I do have positive antibody levels that have been responsive  to a gluten free diet. I can’t help but wonder if the last year has caused all this. 
    • Scott Adams
      I don't think any apps are up to date, which is exactly why this happened to you. Most of the data in such apps is years old, and it doesn't get updated in real time. Ultimately there is no substitution for learning to read labels. The following two lists are very helpful for anyone who is gluten sensitive and needs to avoid gluten when shopping. It's very important to learn to read labels and understand sources of hidden gluten, and to know some general information about product labelling--for example in the USA if wheat is a possible allergen it must be declared on a product's ingredient label like this: Allergens: Wheat.      
×
×
  • 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.