Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Daughter biopsy today!


Jules22

Recommended Posts

Jules22 Apprentice

So my type 1 daughter had her biopsy today and the gi afterwards noticed some redness/inflammation (gastritis?) but also saw the villi.  I guess I was expecting that with her blood test result of her transglutinminase ttg iga of over 100 that she would definitely see some damage.  Her symptoms seem to be ramping up as well.  She took multiple biopsies in several locations and now we wait.  Do you think that there is a chance that with a very positive blood test result she could have a negative biopsy?  My daughter was saying that she would like the positive biopsy to know for sure and to make it easier to stick to being gluten free forever. 

 

This is really hard waiting


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

I hope you don't have to wait too long for the results. A false negative is always possible since we have a lot of intestine but it sounds like you have a good doctor who took lots of biopsies.  Since she had a high positive it would be a good idea for her to do the diet strictly for a few months no matter the results. I hope you get some clear answers and that she is feeling better soon.

cyclinglady Grand Master

My GI told me that everything looked great visually (endoscopy), but my biopsies revealed moderate to severe intestinal damage.  ☹️  You just have to wait for the pathologist's report.  

Jules22 Apprentice

Thanks for the responses raven and cyclinglady!  I guess we just have to wait.  Is it wrong that I want there to be no question that its celiac?  She has had so many symptoms for awhile now--seemingly increasing--but I want there to be no question in her mind that she needs to be gluten-free--you know?

For now we are working on eating gluten-free but I haven't really tackled the whole cross-contamination thing yet and looking into my freezer, fridge and pantry I have a decent amount of gluten that the rest of us will eat.  Then I guess I'll decide how gluten-free the rest of us should be.

On a side note--the gi ran a bunch of tests prior to the biopsy--I haven't seen the results--but they mentioned over the phone that her white blood cells were high--maybe due to celiac?

 

 

cyclinglady Grand Master

I know I needed the confirmation.  My hubby went gluten free per the very poor advice from my allergist and his GP.   It worked, but we really do not know if he has celiac disease.  He refuses to do a gluten challenge and I do not blame him.  We do know that gluten makes him sick.  He has been gluten free for 16 years.  

So, when my GI suspected celiac disease, I could not believe it.  I had no tummy issues at the time, but was anemic.  Had been my whole life and it was blamed on a genetic anemia and menstruation.  I knew what being gluten free meant and I did not want to have celiac disease.  But,   I got positives  on the DGP and my biopsy.    Nothing like seeing something in writing.  I showed that to my extended family who was in denial as well.  

I had a shared household with hubby all those years.  But after my diagnosis and the fact my kid started making things in the kitchen, we all went Gluten Free.  Great kid, but I could not trust her with my health!  If you DD has small siblings, consider all going gluten free.  They can eat gluten outside of the house.  That is what my kid does.  

Jules22 Apprentice

Does a biopsy coming in quick mean anything?  My daughter's GI called today to say that the results are in and asked if she could come in tomorrow---sadly she is working right now and scheduled to work tomorrow and I didn't think I could make that decision for her!  But of course I'm anxious to find out the results--and we weren't scheduled with the GI until next Friday!

 

Also, I came across a video online by a Dr. David Johnson who was talking about celiac biopsy protocols and he said that in a group of people the only atrophy that is found is at the duodenal bulb.  And that should always be a place to be biopsied--along with others.  Looking at the sheet I was given after her procedure--it was noted that she had possible erythematous mucosa at the duodenal bulb but no biopsies were listed as taken.  Other areas had the mucosa found and biopsies there were done.  Several in other areas.  Does this mean that her biopsy might not have been done correctly?

This is such a frustrating diagnosis--and I just need to find out to move forward.

cyclinglady Grand Master

This is beyond my capabilities as I do not wear a white coat.  Best to talk to the GI.  


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



Celiac.com Sponsor (A8-M):



Jules22 Apprentice

Thanks--I understand.  I guess I have never been a very patient person--Lol!

kareng Grand Master
29 minutes ago, Jules22 said:

Does a biopsy coming in quick mean anything?  My daughter's GI called today to say that the results are in and asked if she could come in tomorrow---sadly she is working right now and scheduled to work tomorrow and I didn't think I could make that decision for her!  But of course I'm anxious to find out the results--and we weren't scheduled with the GI until next Friday!

 

Also, I came across a video online by a Dr. David Johnson who was talking about celiac biopsy protocols and he said that in a group of people the only atrophy that is found is at the duodenal bulb.  And that should always be a place to be biopsied--along with others.  Looking at the sheet I was given after her procedure--it was noted that she had possible erythematous mucosa at the duodenal bulb but no biopsies were listed as taken.  Other areas had the mucosa found and biopsies there were done.  Several in other areas.  Does this mean that her biopsy might not have been done correctly?

This is such a frustrating diagnosis--and I just need to find out to move forward.

Probably just means that the lab isn't busy.  Not many people scheduling elective procedures at the end of July.

Jules22 Apprentice

That makes sense--got to stop worrying and thinking about this.  It will be what it will be.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      126,728
    • Most Online (within 30 mins)
      7,748

    Jamie marozza
    Newest Member
    Jamie marozza
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.9k
    • Total Posts
      69.6k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • nanny marley
      I have recently had tests for calprotein in a fecal test has come back apparently high at 2500 and flagged up  stage 3a GKD and GFR  59 and 95 on the serum creatinine the test I was sent for also for milk allergy and celiac hasn't come back yet because it's had to be sent off to a different place I was just wondering if anyone had these addition tests going threw ceilac testing any help would be great 
    • Julie Max
      As far as I know, miso paste is gluten-free and should be added to the Safe List.  And, shouldn't soy sauce be on the Forbidden list?
    • knitty kitty
      @PlanetJanet, Sorry to hear about your back pain.  I have three crushed vertebrae myself.  I found that a combination of Thiamine, Cobalamin and Pyridoxine (all water soluble B vitamins) work effectively for my back pain.  This combination really works without the side effects of prescription and over-the-counter pain meds.  I hope you will give them a try. Here are articles on these vitamins and pain relief... Mechanisms of action of vitamin B1 (thiamine), B6 (pyridoxine), and B12 (cobalamin) in pain: a narrative review https://pubmed.ncbi.nlm.nih.gov/35156556/ And... Role of B vitamins, thiamine, pyridoxine, and cyanocobalamin in back pain and other musculoskeletal conditions: a narrative review https://pubmed.ncbi.nlm.nih.gov/33865694/
    • Scott Adams
      Here is the info from their website. If you don't trust them, you may find products that are labelled "gluten-free," but I don't see any reason to believe there is any gluten in them. Hunt's Tomato Paste: https://www.hunts.com/tomato-sauce-paste/tomato-paste   Hunt's Tomato Sauce: https://www.hunts.com/tomato-sauce-and-paste/tomato-sauce  
    • PlanetJanet
      Hi, trents, Thanks for responding! One book I read is called, Doing Harm, by Maya Dusenbery.  She has wonderful perspective and insight, and it's all research-based.  It's about how women can't get treated.  Everyone should read this!  I wouldn't mind reading it again, even.  She believes that women are so busy taking care of families, working, etc., that we are more likely to ignore our pain and symptoms for longer.  Men have women bugging them to go to the doctor.  Women don't have anyone telling us that.  We don't have time to go.  Providers think we are over-emotional, histrionic, depressed, have low tolerance to pain...Men get prescribed opioids for the same symptoms women are prescribed anti-depressants.  My car crash in January 2020 made going to the doctor a full-time job.  I grew up with 2 rough and tumble brothers, played outside, climbed trees.  I was tough and strong, pain didn't bother me, I knew it would heal.  But do you think I could get treated for back pain--as a woman?  I am so familiar now with the brush-offs, the blank looks, the, "Take your Ibuprofen," the insinuation that I am just over-reacting, trying to get attention, or even, "Drug Seeking."  Took almost 2 years, but what was happening was Degenerative Sacroiliitis.  I couldn't walk right, my gait was off, effected my entire spine because gait was off.  I had braced myself with my legs in a front-impact, slightly head-on crash with someone who made a left turn in front of me from the opposite direction.  I finally had SI Joint Fusion surgery, both sides.  It's not a cure. I have given up on trying to get properly treated.  There is so much pain with these spine issues caused by bad gait:  scoliosis, lithesis, arthropathy, bulged disc, Tarlov cysts.  And I can't take anything because of my bad tummy. Not that I would ever hurt anyone, but I can relate to Luis Mangione who couldn't get treated for his back injury. I feel so alone.
×
×
  • Create New...