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

More Sensitive To Gluten After Being gluten-free?


kpryan

Recommended Posts

kpryan Apprentice

Hi there...my name is Kristin and I am new to this forum.

I've been gluten free for about 2 years now. Despite a negative Celiac blood panel, I decided to go gluten-free after seeing a HUGE improvement in many chronic symptoms I've had for my whole life. I recently too gave up dairy in November of last year after seeing the return of some of those symptoms.

I feel that I am very good at adhering to the diet. With my limited options, I eat a rather predicitable diet.

Question is, lately i've noticed that if I accidentally ingest the tiniest part of gluten, I have a HUGE reaction to it. Much worse than before. Is it possible to become more sensitive to gluten the longer you go without it?

The last 2 weeks I seem to be getting sick frequently again. I've had no obvious gluten accidents. The only thing I can think of is a shared toaster we use at home and a frying pan...though I mainly do the cooking...

Yesterday I got quite ill from some eggs I cooked with pancetta (which I confirmed with the company was gluten-free)....so frustrating when you don't know what is making you sick.

Thanks!


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



Celiac.com Sponsor (A8-M):



Skylark Collaborator

Funny, I came here to ask exactly the same question. I've gotten much more sensitive since I went gluten-free about five years ago. I didn't have to worry about little bits of CC in restaurants or "shared machinery" labels. Now I am reacting to tiny bits of gluten too. It's really a pain.

kpryan Apprentice

It really is such a pain! And then you start second guessing everything! It was definately easier before, though not healthier I realize. But it feels like a kick in the gut (no pun intended) to be so strict with what you eat, and then you end up much more sensitive.

Well I think I'm going to completely make sure everything in my kitchen is ok and see if that helps.

Looking for answers Contributor

You may be having reactions to other foods as well. I went through the same when I was new to the diet, then realized I also am intolerant to dairy, nuts, corn and soy. Also, try taking enzymes and probiotics with each meal...they help.

JNBunnie1 Community Regular

A shared toaster will absolutely gluten you.

It seems, from my experience, that pretty much everyone gets more sensitive the more time passes. It might sound weird, but this is a good thing. Basically, your system was so damaged before that it could only recognize big amounts. Now, your system is healthier, like a machine that's been finely calibrated. It's annoying that you're more sensitive, but it's not a bad thing, health-wise.

conniebky Collaborator

Ya know, I was thinking to myself that I, too, have become more sensitive, but then realized that maybe, just maybe, we don't become more sensitive, it's just that now we realize what it is and that brings it into the spotlight, so to speak.

dilettantesteph Collaborator

I have definitely gotten more sensitive. I am crazy sensitive now. I can't eat most processed things and have to even be careful about my produce. Out of my garden things are fine, but I have to watch out for which companies tomatoes I buy etc. It is a huge pain.


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



Celiac.com Sponsor (A8-M):



jerseyangel Proficient

I'm definitely more sensitive to gluten than I was when I first went gluten-free. I don't use many processed foods, and don't recall a single time I was able to get away with anything made on the same lines as gluten.

I'm 5 years in now, and my sensitivity level is about the same--it kinda leveled out. :D

LynnJ Newbie

I was diagnosed with Celiac in 1964 when I was 5 years old. Throughout most of my childhood my mom made sure I was gluten-free (well, as much as one can be back then). Because of misdiagnosis in my adult years--one doctor told me I did not have Celiac and was not gluten-intolerant--I went off my diet. Needless to say, about 3 years ago at the age of 48, I started exhibiting many of the original symptoms of Celiac and went to see a gastroenterologist, who said my Celiac is quite advanced but had not yet done any irreparable damage (although some issues have now appeared during a recent biopsy of my stomach). I have been on a strict gluten-free lifestyle for most of the time (we all slip up, eh?), but I do notice that I am becoming much more sensitive to even the smallest amounts of gluten.

JAMR Newbie

My reaction to gluten has also increased since eliminating it from my diet around 2 years ago. It is pretty much like an alcoholic reaction. Its possible fomr someone to drink large quantities with a high level of tolerance, once they go teetotal any amount of booze will flatten them. Although your body is being damaged by gluten in a normal gluten type diet, the tolrance is also quite good. Once you free the body from the toxic effect, tissues heal and the systems become more sensitive because of lack of exposure. The moral of the story is that you need to be vigilant all the time, any complacency will set you back because you imagine that feeling better will just keep happening. It doesnt. Also note that reactions can be caused by multiple sensitivities, or foods that have been under the radar because you are so focused on gluten. Although it appears the occasional accidents do not set you back to square one, incremental damage does occur with repeated exposures, as well as often eating too much of some other food increasing your sensitivity. Its certainly not an easy condition to manage.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      128,266
    • Most Online (within 30 mins)
      7,748

    Cindy Whitis
    Newest Member
    Cindy Whitis
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.1k
    • Total Posts
      70.8k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      Sorry but I don't have specific recommendations for doctors, however, starting out with good multivitamins/minerals would make sense. You may want to get your doctor to screen you for where you different levels are now to help identify any that are low, but since you're newly diagnosed within the past year, supplementation is usually essential for most celiacs.
    • trents
      Yes, I can imagine. My celiac journey started with a rejection of a blood donation by the Red Cross when I was 37 because of elevated liver enzymes. I wasn't a drinker and my family doctor checked me for hepatitis and I was not overweight. No answers. I thought no more about it until six years later when I landed a job in a healthcare setting where I got annual CMP screenings as part of my benefits. The liver enzymes were continually elevated and creeping up every year, though they were never super high. My primary care doc had no clue. I got really worried as your liver is pretty important. I finally made an appointment with a GI doc myself and the first thing he did was test me for celiac disease. I was positive. That was in about 1996. After going on a gluten-free diet for three months the liver enzymes were back in normal range. Another lab that had gotten out of whack that has not returned to normal is albumin/total protein which are always a little on the low side. I don't know what that's about, if it's related to the liver or something else like leaky gut syndrome. But my doctors don't seem to be worried about it. One thing to realize is that celiac disease can onset at any stage of life. There is a genetic component but there is also an epigenetic component. That is, the genetic component is not deterministic. It only provides the potential. There needs also to be some health or environmental stressor to activate the latent gene potential. About 40% of the population have the genetic potential to develop celiac disease but only about 1% actually do.
    • cristiana
      Hello @Heather Hill You are most welcome.  As a longstanding member and now mod of the forum, I am ashamed to say I find numbers and figures very confusing, so I rarely stray into the realms of explaining markers. (I've self-diagnosed myself with dyscalculia!)  So I will leave that to @Scott Adams or another person. However as a British person myself I quite understand that the process with the NHS can take rather a long time.  But just as you made a concerted effort to eat gluten before your blood test, I'd advise doing the same with eating gluten before a biopsy, in order to show if you are reacting to gluten.  It might be worth contacting the hospital or your GPs secretary to find out if they know what the current waiting time is. Here is a page from Coeliac UK about the current NHS recommendations. https://www.coeliac.org.uk/information-and-support/coeliac-disease/getting-diagnosed/blood-tests-and-biospy/#:~:text=If you remove or reduce,least six weeks before testing. Cristiana  
    • MI-Hoosier
      Thanks again. My mom was diagnosed over 50 years ago with celiac so grew up watching her deal with the challenges of food. I have been tested a few times prior due to this but these results have me a bit stunned. I have a liver disease that has advanced rapidly with no symptoms and an allergy that could be a contributing factor that had no symptoms. I guess I’ll call it lucky my Dr ordered a rescreen of a liver ultrasound from 5 years ago that triggered this or I would likely have tripped into cirrhosis. It’s all pretty jarring.
    • Heather Hill
      Many thanks for your responses, much appreciated.  The tests did include tTg IgA and all the other markers mentioned.  I also had sufficient total IgA so if I'm reading the Mayo clinic thing correctly, I didn't really need the anti-deaminated gliadin marker? So, if I am reading the information correctly do I conclude that as all the other markers including tTg IgA and DGP IgG and tTg IgG and EMA IgA are all negative, then the positive result for the immune response to gliadin, on it's own, is more likely to suggest some other problem in the gut rather than Coeliac disease? Until I have a view from the medics (NHS UK) then I think I will concentrate on trying to lower chronic inflammation and mend leaky gut, using L glutamine and maybe collagen powder. Thank you for your help so far.  I will get back in touch once I have a response, which sadly can take quite a long time.   Kindest Heather Hill 
×
×
  • Create New...