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

Newly diagnosed, follow up endoscopy in 6 months?


Rosie72

Recommended Posts

Rosie72 Newbie

I was newly diagnosed. My TTG was 54 and my lab work was somewhat confusing. It showed 'mild' damage. My GI doctor also sent the biopsies to another pathologist for a 2nd opinion and they agreed that because of my TTG, I have celiac. I have also found out that it runs in the family on my mother's side. My GI doctor wants me to do the endoscopy again but not the blood work. Is this normal? How often do you follow up with biopsies/bloodwork?

Thanks,


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



Celiac.com Sponsor (A8-M):



Gemini Experienced
1 hour ago, Rosie72 said:

I was newly diagnosed. My TTG was 54 and my lab work was somewhat confusing. It showed 'mild' damage. My GI doctor also sent the biopsies to another pathologist for a 2nd opinion and they agreed that because of my TTG, I have celiac. I have also found out that it runs in the family on my mother's side. My GI doctor wants me to do the endoscopy again but not the blood work. Is this normal? How often do you follow up with biopsies/bloodwork?

Thanks,

It really all depends on the patient. I never had a biopsy because my blood work was off the charts and I was too sick for a biopsy at the time I was diagnosed.  I did so well on the diet, I never felt the need to have one. It has been almost 11 years now and I am still doing well so you can see, it all depends on your experience. If you feel comfortable with the testing and you want to see what your gut looks like after 6 months, then you have the option of doing so.

The blood work should be repeated to make sure your tTg comes down well into the low normal range, at the one year mark. Then after that happens, every 1 to 2 years on the blood work should be fine.

Welcome and good luck!

kareng Grand Master

Maybe share this from Celiac experts with your doctor? 

"New celiacs should receive follow-up testing twice in the first year after their diagnosis. The first appointment should occur 3-6 months after the diagnosis, and the second should occur after 1 year on a gluten-free diet. After that, a celiac should receive follow-up testing on a yearly basis. We recommend checking both tTG and DGP (Deamidated gliadin peptides) at each screening."

 

Open Original Shared Link

 

Once I’ve been biopsy-diagnosed to confirm celiac disease, do I ever need to have another biopsy done?

Provided you received a clear diagnosis and aren’t experiencing issues there’s no reason to have another biopsy. Even though you may not notice any symptoms from consuming gluten, the disease is still active and can lead to severe complications over time if gluten is sneaking into your diet. Therefore, we recommend annual testing to check for elevated antibodies in your blood.

 

Open Original Shared Link

frieze Community Regular

follow the money.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,522
    • Most Online (within 30 mins)
      7,748

    EmilyAnthony
    Newest Member
    EmilyAnthony
    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

    • cristiana
      More great tips, and a good excuse to shop at M&S and also buy more iced buns!   I wish we had an ASDA near us, as the few times we've been to one their gluten-free pasta range seemed very reasonably priced compared to other shops.  Thanks so much, @Russ H.
    • Russ H
      I hope you are on the mend soon. About 1 in 5 people who contracted chicken pox as a child go on to develop shingles in later life - it is not uncommon. There are 5 known members of the herpes virus family including chicken pox that commonly infect humans, and they all cause lifelong infections. The exact cause of viral reactivation as in the case of shingles or cold sores is not well understood, but stress, sunburn and radiotherapy treatment are known triggers. Some of the herpes viruses are implicated in triggering autoimmune diseases: Epstein-Barr virus is suspected of triggering multiple sclerosis and lupus, and there is a case where it is suspected of triggering coeliac disease. As to whether coeliac disease can increase the likelihood of viral reactivation, there have been several cohort studies including a large one in Sweden suggesting that coeliac disease is associated with a moderate increase in the likelihood of developing shingles in people over the age of 50. US 2024 - Increased Risk of Herpes Zoster Infection in Patients with Celiac Disease 50 Years Old and Older Sweden 2018 - Increased risk of herpes zoster in patients with coeliac disease - nationwide cohort study
    • Russ H
      BFree bread is fortified with vitamins and minerals as is ASDA own-brand gluten-free bread. All the M&S bread seems to be fortified also.
    • 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.
×
×
  • 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.