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

Advice please


fancy19

Recommended Posts

fancy19 Rookie

Hi All, 

First time post.  I'm 40, just had my bloodwork done and asked to be tested for celiac as my mother was just diagnosed with silent celiac on biopsy.  My TTG came back at 250 I believe and normal IgA so she is referring me for a biopsy.  I live in Canada and wait times for this will be between 6-12 months.  I'm going to assume theres a decent chance I'm celiac so should I keep eating gluten until the test is done or stop now and reintroduce a couple months before my test.  I'm just scared to damage myself for that long while I wait in chance I'm celiac.  Any other similar stories?

 

Cheers,

FP


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



Celiac.com Sponsor (A8-M):



Victoria1234 Experienced
9 hours ago, fancy19 said:

Hi All, 

First time post.  I'm 40, just had my bloodwork done and asked to be tested for celiac as my mother was just diagnosed with silent celiac on biopsy.  My TTG came back at 250 I believe and normal IgA so she is referring me for a biopsy.  I live in Canada and wait times for this will be between 6-12 months.  I'm going to assume theres a decent chance I'm celiac so should I keep eating gluten until the test is done or stop now and reintroduce a couple months before my test.  I'm just scared to damage myself for that long while I wait in chance I'm celiac.  Any other similar stories?

 

Cheers,

FP

Short answer is YES keep eating gluten until the testing is over. If you go without and reintroduce, your body will react much worse to the gluten. If you have any symptoms now, they will be multiplied. New ones might pop up! This is just what happens to many, many of of here. You don't have to eat much, a sandwich a day will be fine, if you wish to cut back.

take this time to start looking up new recipes, and read up on the 101 topic here on the forums. 

Good luck!

fancy19 Rookie

I also have to mention that I have what my derm says is psoriasis but I"m starting to think maybe related to this with the itchy rashes i get on my butt checks, knees and elbows when I have flares.    I was also a heavy drinker for years before I quit a year ago so I hope its not related to that.

cyclinglady Grand Master

You are in a difficult situation.  I hope another Canadian can offer advice, but in the meantime, I think you have a few options.  You could keep eating gluten until your endoscopy.  You can periodically call to see if there have been cancellations.  You could go gluten free and then reintroduce gluten 2 to 4 weeks prior to the endoscopy to get an accurate result.  You could get your doctor to diagnose you based on a full celiac panel, family history, reaction to the gluten-free diet and follow-up blood tests.  

Only you and your doctor can decide what is best for your current health issues.  

 

Awol cast iron stomach Experienced
3 hours ago, Victoria1234 said:

Short answer is YES keep eating gluten until the testing is over. If you go without and reintroduce, your body will react much worse to the gluten. If you have any symptoms now, they will be multiplied. New ones might pop up! This is just what happens to many, many of us here.

Yes exactly this. I second the motion. My story unfortunately unfolds in a way I went gluten-free out of desperation since my efforts over decades to get help in allopathic medicine failed to connect the gluten /food dots. It was always diagnosed something else. By the time I did my gluten challenge with a Dr.  willing to test me , I was very ill from reintroducing gluten and could not finish the 14 day gluten challenge I was instructed to do. I could only get 6 days as every system in my body revolted badly.

If your body currently has gluten issues the gluten exposure is providing a working around it/ somewhat tolerating it. Since you have a Dr and a celiac positive relative this is progressing well, you can see it through. Those of us who went gluten-free  prior to gold standard testing have a patchwork medical history of misses and misdiagnosis decades long that drove us to going gluten-free prior. Our path is not ideal and is thankful my not yours. Follow Victoria1234 advice.

Eat the required amount the newbie testing thread suggests to stay the course to your scope. To stop gluten then reintroduced is like trying to switch gears with out the clutch. Good luck.

fancy19 Rookie

Thanks for the reply everyone.  Unfortunately the wait time for endosocpy/GI consult in Nova Scotia is at almost 300 days.   Wonder if it would be worth trying to find a private clinic and just pay.

Celiac's Wifey Explorer
On 8/5/2017 at 9:07 AM, fancy19 said:

I"m starting to think maybe related to this with the itchy rashes i get on my butt checks, knees and elbows when I have flares.

I don't know if this would be a faster possible route in Canada or not, but this sounds like possible dermatitis herpetiformis - a skin manifestation of celiac disease. You might want to read up on it and figure out if a scoop skin biopsy of your rash (very important that it be next to a leison NOT on it) would be faster to get than 300 days wait for the endoscopy. A diagnosis of dermatitis herpetiformis is considered a diagnosis of celiac disease. 

Open Original Shared Link

Open Original Shared Link

My husband was diagnosed by skin biopsy as a kid (on the other hand, psoraisis  & celiac are related too  - his dad has both.)


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



Celiac.com Sponsor (A8-M):



  • 2 weeks later...
fancy19 Rookie

Well I had my GI appointment last week, got in quick I suppose as my GP noted some weight loss as well.  GI basically said with my family history and TTG over the max 250 she can diagnose me but still wants to do the biopsy to confirm and get a baseline.  I'm happy with that because I've been having some irritating throat symptoms that kind of bother me and would prefer they have a look at everything.  Even better news is that there is nobody on her cancellation list for a scope so I'm on it and should have it done within the month :)  

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,175
    • Most Online (within 30 mins)
      7,748

    Chels22
    Newest Member
    Chels22
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Heatherisle
      Daughter has started gluten free diet this week as per gastroenterologists suggestion. However says she feels more tired and like she’s been hit by a train. I suggested it could be the change to gluten free or just stress from the endoscopy last week catching up with her. Just wondering if feeling more tired is a normal reaction at this stage. I suppose it’s possible some gluten might have been present without realising. Have tried to reassure her it’s not going to resolve symptoms overnight
    • DAR girl
      Looking for help sourcing gluten-free products that do not contain potato or corn derived ingredients. I have other autoimmune conditions (Psoriatic Arthritis and Sjogrens) so I’m looking for prepared foods as I have fatigue and cannot devote a lot of time to baking my own treats. 
    • Scott Adams
      I am so sorry you're going through this. It's completely understandable to feel frustrated, stressed, and disregarded after such a long and difficult health journey. It's exhausting to constantly advocate for yourself, especially when you're dealing with so many symptoms and positive diagnoses like SIBO, while still feeling unwell. The fact that you have been diligently following the diet without relief is a clear sign that something else is going on, and your doctors should be investigating other causes or complications, not dismissing your very real suffering. 
    • Oldturdle
      It is just so sad that health care in the United States has come to this.  Health insurance should be available to everyone, not just the healthy or the rich.  My heart goes out to you.  I would not hesitate to have the test and pay for it myself.  My big concern would be how you could keep the results truly private.  I am sure that ultimately, you could not.  A.I. is getting more and more pervasive, and all data is available somewhere.  I don't know if you could give a fake name, or pay for your test with cash.  I certainly would not disclose any positive results on a private insurance application.  As I understand it, for an official diagnosis, an MD needs to review your labs and make the call.  If you end up in the ER, or some other situation, just request a gluten free diet, and say it is because you feel better when you don't eat gluten.      Hang in there, though.  Medicare is not that far away for you, and it will remove a lot of stress from your health care concerns.  You will even be able to "come out of the closet" about being Celiac!
    • plumbago
      Yes, I've posted a few times about two companies: Request a Test and Ulta Labs. Also, pretty much we can all request any test we want (with the possible exception of the N protein Covid test and I'm sure a couple of others) with Lab Corp (or Pixel by Lab Corp) and Quest. I much prefer Lab Corp for their professionalism, ease of service and having it together administratively, at least in DC. And just so you know, Request a Test uses Lab Corp and Quest anyway, while Ulta Labs uses only Quest. Ulta Labs is cheaper than Request a Test, but I am tired of dealing with Quest, so I don't use them so much.
×
×
  • Create New...