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

1year post-DX appointment: feeling really nervous!


Juca

Recommended Posts

Juca Contributor

Hi everyone, 

This is going to be a long one, so please bear with me. 

Finally I have my 1 year review appointment next week. As someone who rarely had any GI symptoms (and so had no way to tell if I am getting glutened), I was really looking forward to this day. I really wanted to find out if all the changes I made in my life I had done the trick. Also, because we postponed trying to get pregnant until I was doing better. 

But now, I am scared. And my head is filling up with questions. 

A year ago I had off the chart high blood tests and was a Marsh 3C. Six months ago the blood tests were significantly better but far from good. 

I was feeling quite positive until about 3 weeks ago. Then, I started suffering from bad hay fever (itchy red eyes, blocked drippy nose, itchy palate..) for the first time in my life. Aren't allergies supposed to go away/improve on a gluten-free diet?? Also some little blisters showed up in my hands, which the dermatologist thought might be dermatitis herpetiformis but clearly was far from sure. :blink:

Am I getting glutened? Are the 2 things related or just a big coincidence? If I was glutened recently, will the doctor be able to tell a single episode from how I did the past 6 months? If so, how? 

I am beeing followed by my GP, as it is usually done here. He is a good doctor (for example, he was the one who finally diagnosed me) but, as he admits, has limited experience with celiac disease. So I wanna go there with my homework done:

- what should the celiac disease panel include and how does one interpret it? 

- should he retest iron, vit D, folic acid, etc? 

- is it worth going through a skin biopsy to confirm the dermatitis? It might be my only visible symptom to tell if I am getting glutened...

- should I have a GI biopsy again at some point? How can one tell if  nutrients are being absorbed properly? 

- should I do an "oats" challenge? Haven't risked eating any so far.. 

- what else should I ask about in this appointment? 

This might shock some of you, but sometimes I wish I felt worse when eating gluten. It is so difficult to have this invisible monster, always hanging over your head.. Never knowing if you did enough.. Never knowing who to trust.. :(

Please let me know what you think or how did it go for you, and.. fingers crossed! 

 


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



Celiac.com Sponsor (A8-M):



cyclinglady Grand Master
2 hours ago, Juca said:

Hi everyone, 

This is going to be a long one, so please bear with me. 

Finally I have my 1 year review appointment next week. As someone who rarely had any GI symptoms (and so had no way to tell if I am getting glutened), I was really looking forward to this day. I really wanted to find out if all the changes I made in my life I had done the trick. Also, because we postponed trying to get pregnant until I was doing better. 

But now, I am scared. And my head is filling up with questions. 

A year ago I had off the chart high blood tests and was a Marsh 3C. Six months ago the blood tests were significantly better but far from good. 

I was feeling quite positive until about 3 weeks ago. Then, I started suffering from bad hay fever (itchy red eyes, blocked drippy nose, itchy palate..) for the first time in my life. Aren't allergies supposed to go away/improve on a gluten-free diet?? Also some little blisters showed up in my hands, which the dermatologist thought might be dermatitis herpetiformis but clearly was far from sure. :blink:

Am I getting glutened? Are the 2 things related or just a big coincidence? If I was glutened recently, will the doctor be able to tell a single episode from how I did the past 6 months? If so, how? 

I am beeing followed by my GP, as it is usually done here. He is a good doctor (for example, he was the one who finally diagnosed me) but, as he admits, has limited experience with celiac disease. So I wanna go there with my homework done:

- what should the celiac disease panel include and how does one interpret it? 

- should he retest iron, vit D, folic acid, etc? 

- is it worth going through a skin biopsy to confirm the dermatitis? It might be my only visible symptom to tell if I am getting glutened...

- should I have a GI biopsy again at some point? How can one tell if  nutrients are being absorbed properly? 

- should I do an "oats" challenge? Haven't risked eating any so far.. 

- what else should I ask about in this appointment? 

This might shock some of you, but sometimes I wish I felt worse when eating gluten. It is so difficult to have this invisible monster, always hanging over your head.. Never knowing if you did enough.. Never knowing who to trust.. :(

Please let me know what you think or how did it go for you, and.. fingers crossed! 

 

Welcome!  

If you are experiencing some symptoms (and DH might be one of them), I would not start experimenting with oats.  Wait until after your visit and when you have been symptom free.  

Here is testing information:

Open Original Shared Link

Healing can take time.  Do not fret, if your antibodies are still elevated.  Remember, you are looking for a downward trend.  I waited five years to get another endoscopy but that is because I was experiencing GERD symptoms (new) while  I was on a very strict gluten-free diet.  Turns out my small intestine has healed and my gastritis is not related to a celiac flare-up.  

You can ask for a nutrition panel and check for anemia.  If your anemia has resolved, chances are you are fine in absorbing anything per my doctor.  Of course, periodic exposures to hidden gluten can cause setbacks.  

You have a celiac diagnosis based on intestinal biopsies.  I do not think it is necessary to get a skin biopsy.  

Allergies can develop at anytime and yours may be unrelated to celiac disease. Not everything can be blamed on celiac disease!  ?

I think it was prudent to wait until you get a clean bill of health before getting pregnant.  I am confident that you will be fine.  Just be careful about eating out and limit your exposure to insure a good pregnancy.  Be sure your thyroid is monitored.  

Juca Contributor

Thank you for the positivity, it helps..  ^_^

I was severely anemic, but since I had IV iron, a normal blood test wouldn't mean much. Unless iron doesn't last much in the body, and poor absorption would already show up.. I will find out. 

Same with B12, still having injections. 

Thyroid and liver were normal a year ago. 

I guess I will still try to find a dermatologist that is a little familiar with DH. It is reasonable to skip the biopsy but it can still be useful to get an informed opinion. 

RMJ Mentor

I understand your occasional desire to feel worse when eating gluten.  I don’t have obvious symptoms, so I’ve had to be more and more compulsive about avoiding any trace of contamination to get my antibody levels down to normal.  Maybe there was just one food that was contaminated, but I’ll never know which one.

Juca Contributor

Exactly.. :(

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      129,651
    • Most Online (within 30 mins)
      7,748

    Diana Colvin
    Newest Member
    Diana Colvin
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.2k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • SophiesMom
      I have been looking for new dishes. I was surprised to find dishes made of wheat straw. Are these safe for us? I'm very careful to avoid products that may contain gluten. I never thought I might have to check for wheat in dishes.
    • trents
      Welcome to the forum, @Hope07! The reference range would refer to what is considered normal in healthy people. So, 7 or less would mean there is no indication of "active" celiac disease. Apparently, you are doing very will in avoiding gluten. The "Tissue Transglutaminase IGA" is the centerpiece antibody test that clinicians run when checking for celiac disease. My only reservation would be that whenever the TTG-IGA test is run, a "total IGA" test should also be run to check for IGA deficiency. When IGA deficiency is present, other IGA tests, such as the TTG-IGA can be artificially low and result in false positives. In the absence of any symptoms indicating your celiac disease is not under control, however, I would take the result you posted at face value.
    • StevieP.
      Going on a cruise next week and I’m a celiac. Bought a bottle of GliandinX. Should I just take two tablets per day as a precaution? Never tried this before!! Any help is appreciated!!
    • Hope07
      Hola! Not sure if I’m asking this in the right place so apologies if not! I just had a full blood count as part of my first check up after being diagnosed with celiac disease 7 years ago!! With Covid lockdowns then living in Spain for 3 years and now back in the UK, I kept getting missed in the system but finally I’ve had a check up! Does anyone know what this means?  Tissu transglutaminase IgA lev:  0.30 U/ml Reference range:  Below 7 Thank you!   
    • DebD5
      Thank you so very much. 
×
×
  • Create New...