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.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,110
    • Most Online (within 30 mins)
      7,748

    Pumpkin68
    Newest Member
    Pumpkin68
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Xravith
      My genetic test results have arrived - I’m homozygous for DQB1*02, meaning I have HLA-DQ2. I’ve read that this is one of the genes most strongly associated with celiac disease, and my symptoms are very clear. I’m relieved that the results finally arrived, as I was getting quite worried since my symptoms have been getting worse. Next step, blood test. What do these results imply? What should I tell my family? I’m concerned that this genetic predisposition might also affect other family members.
    • Roses8721
      Two months. In extreme situations like this where it’s clearly a smoking gun? I’m in LA so went to a very big hospital for pcp and gi and nutritionist 
    • rei.b
      So far 3 months in - worsening symptoms. I have had the worst constipation in my life and I am primarily eating naturally gluten-free foods like potatoes, eggs, salad with homemade dressing, corn tortillas, etc. I hate gluten-free bread and pasta so I don't eat it. Occasionally I eat gluten-free almond flour crackers. As stated in the post, I don't have any vitamin deficiency. I was already tested.
    • rei.b
      As I said, I do not have any vitamin deficiency. I was already tested.
    • Wheatwacked
      Talk to your  Talk to your provider about testing for vitamin and mineral deficiency.  celiac disease causes malabsorption and eventually malnutrition.  Especially vitamin D. Having the gallbladder removed seems to be a common step on the way to a Celiac Disease Diagnosis,  Gallbladder is a sympton of deficient Choline. Eggs and red meat are the primary source..Choline makes up a majority of the bile salts.  The bile gets thick, doesn't get enough into intestine to digest fats well.  Can eventually back up into gallbladder, cause gallstones.  Without bile, bowel movements can become hard. Try to avoid all processed foods while you are healing, The gluten-free foods are not fortified with vitamins and use various ingredients to mimic fat that bothers many Celiacs.  Choose vegatables with low omega 6.  Optimum omega 6 to omega 3 ratio is less than 3:1.  Wheat flour is 22:1.  Grass fed milk is 1:1.   Commercial Dairies milk is 5:1.  They feed wheat, rye and barley Gluten as part of the food mix.  
×
×
  • 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.