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

Is It Weird To React To Wheat Only Most Of The Time?


SeattleGF

Recommended Posts

SeattleGF Newbie

Hey folks! I'm new to the boards. I'm 36 years old, mother of two. About 7 months ago I was having all kinds of physical sensations that for years I'd attributed to panic disorder and generalized anxiety disorder. Yet medications and therapy didn't work, the sensations and "attacks" were always happening, no matter how well I did the exercises or worked with my doctor. Finally my GP suggested I go off gluten, even though a blood test didn't show signs of celiac.

For about six days I felt awful, but then after that, I began to feel better, and better, and better, until finally I was almost totally without any of the previous symptoms I'd lived with for so long. Now, I do still have problems with anxiety, but they're totally unconnected to food and only happen in certain known circumstances - being stuck in traffic, for example. What used to be a constant struggle that left me housebound basically lifted. It felt miraculous, to myself and my family.

The other miraculous thing was that dairy, which I'd been unable to eat for years, I was now able to eat with abandon! It's been incredible! I haven't eaten dairy in years, and now I can eat cheese and milk without spending an hour in the bathroom or feeling sick for a day. My doctor said that she couldn't diagnose me with celiac officially, not without doing the bowel biopsy which would be a miserable thing to go through, however the fact that after six weeks of being gluten-free I was able to eat dairy strongly suggested to her that having celiac was the issue. She said I should stay off gluten for the rest of my life and be grateful.

Anyway, it's been a great 7 months, full of eating cheese again and feeling better than I have in years. So what's my question....

Well, most of the time when I get accidentally "glutened", I know it. The way I know it isn't bowel pain like most people, it's actually a rapid heart rate, a sense of being "out of it" (like a carb coma), and low-level anxiety, among other things - I even sometimes get flashes of heat, and my blood pressure will go up. Usually when this happens I end up looking back and realizing that I got glutened,either at a restaurant or from some packaged food we didn't check carefully enough.

But SOMETIMES, rarely, but it's happened, I've gotten glutened and nothing has happened. Nothing at all. This happened the other night when I poured what I thought was gluten-free pasta into the soup I was making for dinner. It's semolina pasta, which I've read has a high gluten content. I didn't realize until after I'd had a big bowl, and it was 24 hours later. I thought back through the last 24 hours, and nothing had happened. This happened a few weeks before, too, when we'd bought two packs of identical snickerdoodles at our local grocery store - one gluten-free, one not. I ended up eating three small cookies from the non-gluten-free box accidentally (we're sure it happened, my husband saw me take them from the wrong box).

So what's the deal? Is it weird to get a reaction from gluten 90% of the time, but then every so often eat a good helping of wheat or gluten and not have anything happen?


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



Celiac.com Sponsor (A8-M):



rainer83 Newbie

I find wheat gives me the worse reactions within about an hour of eating it if I didn't know it was in whatever I ate. I remember before I was diagnosed, Special K and Mini Wheats would have me crying in pain within an hour. Barley doesn't react as quickly, it's probably about 4 hours after I've eaten it. I found this out eating Corn Flakes, not realizing it had malted barley. It effected me for the rest of the day and a few days after though. Not as painful. I could deal with it and move on with my day. Though with wheat? No way. It's actually debilitating. I have a hard time breathing, my entire abdomen swells and I'm down for the count. I can't function at all. I know of other celiacs who have the same problem though. You're not alone.

Although I will recommend to try and stick gluten free even if it doesn't bother you. It's still doing damage to your intestines, whether you feel it or not.

flutterby Apprentice

Although I will recommend to try and stick gluten free even if it doesn't bother you. It's still doing damage to your intestines, whether you feel it or not.

Agreed. See this video for more info:

A lot of the times I have different reactions, depending on what else I've eaten.

Even 1.5 years after going 'gluten' free, I felt great but had an episode of getting suddenly sick and having to go to the doctor, who told me ... be more careful with your diet! I was getting a lot of CC, apparently.

sahm-i-am Apprentice

I have no reactions when I eat gluten that I can see - but the silent war is going on in my small intestine. It is so hard to stay away from gluten for me, because of this, but if I don't many terrible things could happen in my future! The women in my family live well into their 90's. I don't want to break that cycle! ;)

Marz Enthusiast

The way I know it isn't bowel pain like most people, it's actually a rapid heart rate, a sense of being "out of it" (like a carb coma), and low-level anxiety, among other things - I even sometimes get flashes of heat, and my blood pressure will go up.

Wow, that's a great description of what I sometimes have! Is the reaction fairly quick for you, or does it only happen a few hours later?

I've noticed my reactions vary wildly - it can be the above symptoms, or it can be nausea and stomach pain, or cramping/pain/d. I can even have no symptoms, and then get a nasty outbreak of DH. So don't think you can really predict it unfortunately.

When I did a gluten challenge a few months ago, I didn't even get a very noticable reaction to semolina wheat (that I had 3 times a day). But I started feeling really crap and out of it, and a few days later the stomach problems started in earnest.

Do you not get any stomach problems at all? Even 3 to 5 days later (Can be very delayed depending on your system).

rainer83 Newbie

Agreed. See this video for more info:

A lot of the times I have different reactions, depending on what else I've eaten.

Even 1.5 years after going 'gluten' free, I felt great but had an episode of getting suddenly sick and having to go to the doctor, who told me ... be more careful with your diet! I was getting a lot of CC, apparently.

Thanks for sharing the video!

Cross contamination is ridiculous. I can't believe how much of it there is in so many foods. I can't eat Quaker Oatmeal because of all the cross contamination. Even when you read the labels of things that don't have any wheat/gluten, but has been processed in a factory with it.

Skylark Collaborator

It's inconsistent for me too. Last time I ate some wheat by mistake (got the wrong crackers) the only thing that happened was a little canker sore. I was really surprised since I've had D in the past from only fryer CC. It's really inconsistent, but I'm always glad when I make a mistake and don't pay too badly.


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



Celiac.com Sponsor (A8-M):



Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,543
    • Most Online (within 30 mins)
      7,748

    yfuvhg
    Newest Member
    yfuvhg
    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

    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
    • Jsingh
      Hi,  I care for my seven year old daughter with Celiac. After watching her for months, I have figured out that she has problem with two kinds of fats- animal fat and cooking oils. It basically makes her intestine sore enough that she feels spasms when she is upset. It only happens on days when she has eaten more fat than her usual every day diet. (Her usual diet has chia seeds, flaxseeds, and avocado/ pumpkin seeds for fat and an occasional chicken breast.) I stopped using cooking oils last year, and when I reintroduced eggs and dairy, both of which I had held off for a few months thinking it was an issue of the protein like some Celiac patients habe mentioned to be the case, she has reacted in the same fashion as she does with excess fats. So now I wonder if her reaction to dairy and eggs is not really because of protein but fat.   I don't really have a question, just wondering if anyone finds this familiar and if it gets better with time.  Thank you. 
    • Chanda Richard
      Hello, My name is Chanda and you are not the only one that gose through the same things. I have found that what's easiest for me is finding a few meals each week that last. I have such severe reactions to gluten that it shuts my entire body down. I struggle everyday with i can't eat enough it feels like, when I eat more I lose more weight. Make sure that you look at medication, vitamins and shampoo and conditioner also. They have different things that are less expensive at Walmart. 
    • petitojou
      Thank you so much! I saw some tips around the forum to make a food diary and now that I know that the community also struggles with corn, egg and soy, the puzzle pieces came together! Just yesterday I tried eating eggs and yes, he’s guilty and charged. Those there are my 3 combo nausea troublemakers. I’m going to adjust my diet ☺️ Also thank you for the information about MCAS! I’m from South America and little it’s talked about it in here. It’s honestly such a game changer now for treatment and recovery. I know I’m free from SIBO and Candida since I’ve been tested for it, but I’m still going to make a endoscopy to test for H. Pylori and Eosinophilic esophagitis (EoE). Thank you again!! Have a blessed weekend 🤍
    • knitty kitty
      Yes, I, too, have osteoporosis from years of malabsorption, too.  Thiamine and magnesium are what keep the calcium in place in the bones.  If one is low in magnesium, boron, selenium, zinc, copper, and other trace minerals, ones bone heath can suffer.  We need more than just calcium and Vitamin D for strong bones.  Riboflavin B 2, Folate B 9 and Pyridoxine B 6 also contribute to bone formation and strength.   Have you had your thyroid checked?  The thyroid is important to bone health as well.  The thyroid uses lots of thiamine, so a poorly functioning thyroid will affect bone heath.  
×
×
  • 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.