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

Another Question About Reactions


CMCM

Recommended Posts

CMCM Rising Star

Just wondering here....if you have been gluten free (or relatively so) for a few weeks, and then if you get some gluten (small amount, not intentionally) accidentally....would the reaction be GREATER and more noticeable than it would have been when you were eating gluten all the time?

I'm sort of feeling that since I've been gluten free, I'm suddenly more reactive to any that I happen to get. Or maybe it's my imagination.


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



Celiac.com Sponsor (A8-M):



aikiducky Apprentice

Yup, that's how it works for me, too.

I figure if you get gluten all the time, the immune system sorta gets tired of reacting all the time and doesn't react so strongly anymore. When you are gluten free for a while, your immune system gets back it's strength... add gluten, and voilá, a big reaction.

Pauliina

Carriefaith Enthusiast
Just wondering here....if you have been gluten free (or relatively so) for a few weeks, and then if you get some gluten (small amount, not intentionally) accidentally....would the reaction be GREATER and more noticeable than it would have been when you were eating gluten all the time?
When, I was eating gluten before I was diagnosed, I was sick all the time, but it was a constant sick. Almost every day I had extreme fatigue, gas, bloating, diarrhea, and brain fog, and I also experienced other symptoms like bone pain and hair loss. Now, when I get very small amounts of gluten in my system, my body responds quite differently. I still get some of the old symptoms, but I got new ones and one can be quite severe. I now expereince heart palpitations, red bumps on my skin, mild insomnia, which I don't remember having before, and mild to severe upper abdominal stomach pain. The pain in my stomach can be so severe that I can't move and it comes on that strong with little or no warning.
jerseyangel Proficient

I'm noticing that I now get heart palpitations, too, when glutened. My reactions now are more clear cut--nausea, slight D for a few days, upper abdominal pain, thirst, fatigue and the brain fog returns but not as bad as before. Someone described that their tongue feels "too big for their mouth"--thats how I get. Before, as the others, I felt sick all the time--it was more of a degree of how sick I was on any given day.

key Contributor

I had all the gas, bloating, nausea(sort of constant low grade), heart burn, belching, bone pain, bruising, anxiety(low grade), abdominal pain at night especially and IBS (back and forth between D and C). Now when I get gluten, I start belching, VERY nauseated (worst symptom), bloating, then IBS symtpoms again for a few weeks, bone pain and fatigue. For me the next day after getting gluten, I am starving as if I am pregnant or haven't eaten for a week! Weird. Also my heart races for awhile after eating gluten.

Just thought I would give my experience.

Definitely sicker and my GI says this happens.

Monica

CMCM Rising Star

And I noticed last night, in addition to the nausea, I just felt really weird....my lips were almost numb, fingers and feet tingling, felt weak, definite palpitations, mildly dizzy. But no real D or digestive distress at that point. In the past I've had that horrible pain, not exactly in the stomach but higher up. I always assumed it was some sort of heartburn, but then not really that either, and heartburn meds did zero to help it. Sometimes it would be really acute for several hours, but then would hurt to a lesser degree for a couple of days sometimes. And I could NEVER figure out what triggered it because I hadn't eaten the type of foods that should trigger heartburn.

What's really discouraging to me at this point is the feeling that aside from some simple meats, some but not all veggies (I can't eat my much loved potatoes, for example) and limited fruits, there's nothing I can eat anymore, everything makes me feel bad one way or another. Sometimes I wish I could just take a pill and never have to eat anything at all. :(

Carriefaith Enthusiast
In the past I've had that horrible pain, not exactly in the stomach but higher up. I always assumed it was some sort of heartburn, but then not really that either, and heartburn meds did zero to help it. Sometimes it would be really acute for several hours, but then would hurt to a lesser degree for a couple of days sometimes. And I could NEVER figure out what triggered it because I hadn't eaten the type of foods that should trigger heartburn.
My pain is also higher up, the pain is upper abdominal directly below the sternum of the rib cage, I'm pretty sure that it is the stomach but, it could also be the pancreas.

What's really discouraging to me at this point is the feeling that aside from some simple meats, some but not all veggies (I can't eat my much loved potatoes, for example) and limited fruits, there's nothing I can eat anymore, everything makes me feel bad one way or another
I used to feel that way too, but after being gluten free for a year, everything started to get better and I could enjoy eating again without worrying about getting sick.

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



Celiac.com Sponsor (A8-M):



jerseyangel Proficient

Boy--This discussion is really helping me out. I hate that all of us have to experience these things, but it helps so much to know that I'm not alone. Like the palpitations--until recently, I never thought they were connected to Celiac. Also, the belching (sorry!)--I never used to belch even when I was sick. But now, it will come out of nowhere and so embarassing if someone's around. I think I'd probably go nuts if I didn't have you guys to bounce these things off of.

Fluffyblue Newbie

I think that when you are eating gluten all the time, you tend not to notice some of the symptoms because you have them all the time and just live with them, and also you get used to the pain in some respects, so when you go gluten-free, you feel better than you have for ages - hence a little bit of gluten ingested when you are gluten free feels worse than it would do if you were eating it constantly and makes the symptoms seem more pronounced.

However, I have recently had to go on the gluten challenge as my doc told me to get a blood test whilst I was gluten-free - which of course came back negative. Since going on the challenge I have had loose stools where as previously I had constipation more often than not, so I think my reaction is more pronounced. I may of course not be coeliac though in any event.

KaitiUSA Enthusiast

I saw a greater sensitivity to gluten. Some people do not though...it's just one of those things that varies.

CMCM Rising Star
Boy--This discussion is really helping me out. I hate that all of us have to experience these things, but it helps so much to know that I'm not alone. Like the palpitations--until recently, I never thought they were connected to Celiac. Also, the belching (sorry!)--I never used to belch even when I was sick. But now, it will come out of nowhere and so embarassing if someone's around. I think I'd probably go nuts if I didn't have you guys to bounce these things off of.

That's really funny about the belching ...my mom was just telling me a story about when I was around 6, and we had all been sick with some sort of flu, and we were all better including me, but I starting belching LOUDLY and violently to the point they took me to the doctor about it, and it went on for quite a long time. I don't remember that, and haven't noticed it as a problem since then, though. But it was pronounced and weird enough that my mom always remembered it and was puzzled by it, as were the doctors. That would have been about 1955 or so, and virtually nothing was known about celiac then. :lol:

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - trents replied to Sarah Grace's topic in Related Issues & Disorders
      26

      Headaches / Migraines and Hypoglycaemia

    2. - knitty kitty replied to Sarah Grace's topic in Related Issues & Disorders
      26

      Headaches / Migraines and Hypoglycaemia

    3. - trents replied to Sarah Grace's topic in Related Issues & Disorders
      26

      Headaches / Migraines and Hypoglycaemia

    4. - Scott Adams replied to Russ H's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      1

      KAN-101 Treatment for Coeliac Disease

    5. - Scott Adams replied to miguel54b's topic in Related Issues & Disorders
      1

      Body dysmorphia experience


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,152
    • Most Online (within 30 mins)
      7,748

    denise.milillo
    Newest Member
    denise.milillo
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • trents
      This article does not address migraines at all.  Yes, red wine and sulfites are often mentioned in connection with migraine triggers. With me, any kind of alcoholic beverage in very modest amounts will reliably produce a migraine. Nitrous oxide generators, which are vaso dialators, also will give me migraines reliably. So, I think most of my migraines are tied to fluctuations vascular tension and blood flow to the brain. That's why the sumatriptan works so well. It is a vaso constrictor. 
    • knitty kitty
      Excessive dietary tyrosine can cause problems.  Everything in moderation.   Sulfites can also trigger migraines. Sulfites are found in fermented, pickled and aged foods, like cheese.  Sulfites cause a high histamine release.  High histamine levels are found in migraine.  Following a low histamine diet like the low histamine Autoimmune Protocol diet, a Paleo diet, helps immensely.    Sulfites and other migraine trigger foods can cause changes in the gut microbiome.  These bad bacteria can increase the incidence of migraines, increasing histamine and inflammation leading to increased gut permeability (leaky gut), SIBO, and higher systemic inflammation.   A Ketogenic diet can reduce the incidence of migraine.  A Paleo diet like the AIP diet, that restricts carbohydrates (like from starchy vegetables) becomes a ketogenic diet.  This diet also changes the microbiome, eliminating the bad bacteria and SIBO that cause an increase in histamine, inflammation and migraine.  Fewer bad bacteria reduces inflammation, lowers migraine frequency, and improves leaky gut. Since I started following the low histamine ketogenic AIP paleo diet, I rarely get migraine.  Yes, I do eat carbs occasionally now, rice or potato, but still no migraines.  Feed your body right, feed your intestinal bacteria right, you'll feel better.  Good intestinal bacteria actually make your mental health better, too.  I had to decide to change my diet drastically in order to feel better all the time, not just to satisfy my taste buds.  I chose to eat so I would feel better all the time.  I do like dark chocolate (a migraine trigger), but now I can indulge occasionally without a migraine after.   Microbiota alterations are related to migraine food triggers and inflammatory markers in chronic migraine patients with medication overuse headache https://pmc.ncbi.nlm.nih.gov/articles/PMC11546420/  
    • trents
      Then we would need to cut out all meat and fish as they are richer sources of tyrosine than nuts and cheese. Something else about certain tyrosine rich foods must be the actual culprit. 
    • Scott Adams
      I agree that KAN-101 looks promising, and hope the fast track is approved. From our article below: "KAN-101 shows promise as an immune tolerance therapy aiming to retrain the immune system, potentially allowing safe gluten exposure in the future, but more clinical data is needed to confirm long-term effects."  
    • Scott Adams
      Thank you so much for having the courage to share this incredibly vivid and personal experience; it's a powerful reminder of how physical ailments can disrupt our fundamental sense of self. What you're describing sounds less like a purely psychological body dysmorphia and more like a distinct neurological event, likely triggered by the immense physical stress and inflammation that uncontrolled celiac disease can inflict on the entire body, including the nervous system. It makes complete sense that the specific sensory input—the pressure points of your elbows on your knees—created a temporary, distorted body map in your brain, and the fact that it ceased once you adopted a gluten-free diet is a crucial detail. Your intuition to document this is absolutely right; it's not "crazy" but rather a significant anecdotal data point that underscores the mysterious and far-reaching ways gluten can affect individuals. Your theory about sensory triggers from the feet for others is also a thoughtful insight, and sharing this story could indeed be validating for others who have had similar, unexplainable sensory disturbances, helping them feel less alone in their journey.
×
×
  • 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.