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

How Often Do You Get Glutened?


Crayons574

Recommended Posts

Crayons574 Contributor

On average, how often do you get glutened? (This includes being careful about CC, etc.)


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



Celiac.com Sponsor (A8-M):



NorthernElf Enthusiast

These days I am so careful that I rarely get glutened. However, once in awhile - probably every few months or so - I get hit. I do live in a gluten household, although I have specific counters and cookware for myself. Sometimes I don't realize I've been hit until a couple of days afterwards. I'm just getting over a glutening right now. My symptoms were extreme fatigue, extreme crabbiness :angry: (I just wanted to be left alone), a night of stomach cramps (should have been the tip off), and some bathroom issues. :P I am a fitness instructor and I almost passed out in one of my classes - got very light headed and had to stop moving for a few minutes and just tell the class what to do. Never happened to me before !

One of two things got me - I made my chocolate chip cookies with M&M baking bits (safe) and Great Value brand butterscotch chips...might have been the GV chips but they usually say gluten in the ingredients if there is any. More likely the culprit was the hard candy I nibbled on at work...it was hommade and looked to be all sugar but was probably made in a gluteny pan. Those kind of risks are what usually get me - I usually avoid anything homemade unless I made it. I am usually super careful - my downfall is when I am hungry. I never intentionally gluten myself - it's so not worth it. I guess one should assume nothing is safe unless it is labelled gluten-free or confirmed gluten-free online.

tarnalberry Community Regular

Once or twice a year, usually from contamination at a restaurant (though I got out to eat more like once a month).

LDJofDenver Apprentice

I'm kind of like NorthernElf -- I'm careful, but something sneaks in and gets me every couple of months. Usually not at home, as we're pretty on top of things in the homestead (I'm gluten free, my husband is not). Last time was at a friend's house, she was sure she made something "safe" (a crock pot dish with rice, chicken, squash and other vegetables). Either was some spice she used, or brand of chicken broth, or perhaps she'd previously made something with flour or pasta in the crock pot and traces remained. Oh well, I took the risk - and didn't want to scrutinize every container and spice bottle she used - so I paid the piper. Time before that was at a restaurant that reportedly had a gluten free menu -- something obviously cross-contaminated in the kitchen or handling.

I'm pretty careful, but in spite of that it happens once in a while. I guess if we never ate out anywhere or at anyone's house I could eliminate even that but, hey, you've got to live. For all the times we eat out, contamination really is a pretty rare occurrence.

lizard00 Enthusiast

My last glutening was a couple of months ago from a restaurant... which is usually where it happens. Our house isn't totally gluten-free, but anything that has gluten is prepackaged. Nothing that has gluten in it gets cooked here. That significantly cuts down the risk off CC.

maile Newbie

right now, too often. I also live in a mixed household and am careful but occasionally get glutened. I'm not sure what did it this time, but this week was horrible, D, bloating, cramps, nauseau, cranky, anxious. I cut down to rice and vegetables for 2 days to try and clear my system, think I'll go another couple of days <_<

plus I also found out there's a good chance that this drug I take for cystic acne is NOT gluten free in the 100mg size...annoying

oceangirl Collaborator

More often than I'd like-probably once or twice every two months. Often I cannot trace the culprit but I think it might be linked to the rare occasions my spousal equivalent eats gluten.(He usually doesn't) He is incredibly careful, brushes and flosses afterward, but I think that cakes or cookies or bread is difficult to free yourself of somehow. To speak plainly, if we are intimate after he's eaten gluten, there is a strong correlation in a glutening- excellent incentive for him to avoid it.

We live in a gluten-free house, RARELY eat out and make almost all our food from whole ingredients so it is frustrating at times. I will add that I am HIGHLY sensitive which will teach me to have silently scoffed at the thought of such miniscule (sp?) CC when I was first diagnosed. I still keep a food log and that is still helpful at times. I HATE gluten- it scares me because the symptoms are so intense and persistent.

lisa


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

More often than I care to admit at this stage of the game. :ph34r:

Seriously though, it is usually when I am careless in reading a package, want an item so bad that I don't check on 'natural flavors' before I eat it or when I eat something that is 'processed on a shared line with...' (those don't get me all the time so it's like playing roulette). So a lot depends on how much processed foods I have been eating.

peacebwu Rookie

These days I am so careful that I rarely get glutened. However, once in awhile - probably every few months or so - I get hit. I do live in a gluten household, although I have specific counters and cookware for myself. Sometimes I don't realize I've been hit until a couple of days afterwards. I'm just getting over a glutening right now. My symptoms were extreme fatigue, extreme crabbiness :angry: (I just wanted to be left alone), a night of stomach cramps (should have been the tip off), and some bathroom issues. :P I am a fitness instructor and I almost passed out in one of my classes - got very light headed and had to stop moving for a few minutes and just tell the class what to do. Never happened to me before !

One of two things got me - I made my chocolate chip cookies with M&M baking bits (safe) and Great Value brand butterscotch chips...might have been the GV chips but they usually say gluten in the ingredients if there is any. More likely the culprit was the hard candy I nibbled on at work...it was hommade and looked to be all sugar but was probably made in a gluteny pan. Those kind of risks are what usually get me - I usually avoid anything homemade unless I made it. I am usually super careful - my downfall is when I am hungry. I never intentionally gluten myself - it's so not worth it. I guess one should assume nothing is safe unless it is labelled gluten-free or confirmed gluten-free online.

peacebwu Rookie

Fairly new to this, from your post it sounds like you really know what your doing on the "what to eat" end.....can you give us all a list of what you eat each da/week...or some ideas???? Anyone else have any suggestions on eating what?????? Just trying to find something that agrees??? Thanks! d

WW340 Rookie

I rarely ever get glutened anymore. If I do it is from eating in an unfamiliar restaurant, which I totally try to avoid. I know which restaurants I can trust locally, and they know me. I cook everything fresh at home, and my family eats what I cook. They have their bread, crackers and cereal, but that is it. I take food with me to friend and family gatherings, so I don't have to worry about eating there.

mattathayde Apprentice

at home basically never (any issue i have seems to be from other stuff), at school (in my own apartment) i get sick more often but i am not sure if its really gluten or just stress and other sensitivities (i eat a lot of peppers and onions at school and i think i am going to try to lay off them when i go back). when i eat out, i have probably a 10% rate with it but i also have other stuff i think that causes me illness.

my symptoms are so unspecific its hard to tell (lower GI issues) and if i have eaten gluten more than once i get a little bit of brain fog and slight depression

ive been home for a month from school and the only time ive been glutened was after going to outback i think

-matt

chatycady Explorer
Fairly new to this, from your post it sounds like you really know what your doing on the "what to eat" end.....can you give us all a list of what you eat each da/week...or some ideas???? Anyone else have any suggestions on eating what?????? Just trying to find something that agrees??? Thanks! d

Here is what I eat. I haven't been glutened in a year or more.

eggs boiled, poached or scramble in butter - no milk.

all fresh or frozen fruit without sugar or syrup.

home made yogurt with honey.

pork steak, chops or roast

beef roast, steak or hamburger

chicken - be careful - chicken is tricky as it's injected with "stuff" (gluten?)

orange roughy - my favorite fish

shrimp

all fresh and frozen veggies, except potatos sweet and regular, and yams(too starchy)

fresh baked goodies made with almond flour only.

olives, pickles, carrots, celery, - satisfies me when I get the munchies.

Does that give you some ideas? It's all regular food and doesn't cost an arm and a leg, except the almond flour. It's not cheap.

I pretty much shop on the outside asiles of the grocery store. Produce, meat, dairy aisles is where I hang out! I do drink a diet 7-up once in awhile. The key to this gluten free diet is to stock up on food you can eat. If you have something handy you might not feel sorry for yourself and say "There is nothing here for me to eat!" Boo Hoo! It works for me.

Hope this is helpful. Remember it's only food! No big deal.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,901
    • Most Online (within 30 mins)
      7,748

    tessycork47
    Newest Member
    tessycork47
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • 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
      Welcome to the forum, @Judy M! Yes, he definitely needs to continue eating gluten until the day of the endoscopy. Not sure why the GI doc advised otherwise but it was a bum steer.  Celiac disease has a genetic component but also an "epigenetic" component. Let me explain. There are two main genes that have been identified as providing the "potential" to develop "active" celiac disease. We know them as HLA-DQ 2.5 (aka, HLA-DQ 2) and HLA-DQ8. Without one or both of these genes it is highly unlikely that a person will develop celiac disease at some point in their life. About 40% of the general population carry one or both of these two genes but only about 1% of the population develops active celiac disease. Thus, possessing the genetic potential for celiac disease is far less than deterministic. Most who have the potential never develop the disease. In order for the potential to develop celiac disease to turn into active celiac disease, some triggering stress event or events must "turn on" the latent genes. This triggering stress event can be a viral infection, some other medical event, or even prolonged psychological/emotional trauma. This part of the equation is difficult to quantify but this is the epigenetic dimension of the disease. Epigenetics has to do with the influence that environmental factors and things not coded into the DNA itself have to do in "turning on" susceptible genes. And this is why celiac disease can develop at any stage of life. Celiac disease is an autoimmune condition (not a food allergy) that causes inflammation in the lining of the small bowel. The ingestion of gluten causes the body to attack the cells of this lining which, over time, damages and destroys them, impairing the body's ability to absorb nutrients since this is the part of the intestinal track responsible for nutrient absorption and also causing numerous other food sensitivities such as dairy/lactose intolerance. There is another gluten-related disorder known as NCGS (Non Celiac Gluten Sensitivity or just, "gluten sensitivity") that is not autoimmune in nature and which does not damage the small bowel lining. However, NCGS shares many of the same symptoms with celiac disease such as gas, bloating, and diarrhea. It is also much more common than celiac disease. There is no test for NCGS so, because they share common symptoms, celiac disease must first be ruled out through formal testing for celiac disease. This is where your husband is right now. It should also be said that some experts believe NCGS can transition into celiac disease. I hope this helps.
    • Judy M
      My husband has had lactose intolerance for his entire life (he's 68 yo).  So, he's used to gastro issues. But for the past year he's been experiencing bouts of diarrhea that last for hours.  He finally went to his gastroenterologist ... several blood tests ruled out other maladies, but his celiac results are suspect.  He is scheduled for an endoscopy and colonoscopy in 2 weeks.  He was told to eat "gluten free" until the tests!!!  I, and he know nothing about this "diet" much less how to navigate his in daily life!! The more I read, the more my head is spinning.  So I guess I have 2 questions.  First, I read on this website that prior to testing, eat gluten so as not to compromise the testing!  Is that true? His primary care doctor told him to eat gluten free prior to testing!  I'm so confused.  Second, I read that celiac disease is genetic or caused by other ways such as surgery.  No family history but Gall bladder removal 7 years ago, maybe?  But how in God's name does something like this crop up and now is so awful he can't go a day without worrying.  He still works in Manhattan and considers himself lucky if he gets there without incident!  Advice from those who know would be appreciated!!!!!!!!!!!!
    • Scott Adams
      You've done an excellent job of meticulously tracking the rash's unpredictable behavior, from its symmetrical spread and stubborn scabbing to the potential triggers you've identified, like the asthma medication and dietary changes. It's particularly telling that the rash seems to flare with wheat consumption, even though your initial blood test was negative—as you've noted, being off wheat before a test can sometimes lead to a false negative, and your description of the other symptoms—joint pain, brain fog, stomach issues—is very compelling. The symmetry of the rash is a crucial detail that often points toward an internal cause, such as an autoimmune response or a systemic reaction, rather than just an external irritant like a plant or mites. I hope your doctor tomorrow takes the time to listen carefully to all of this evidence you've gathered and works with you to find some real answers and effective relief. Don't be discouraged if the rash fluctuates; your detailed history is the most valuable tool you have for getting an accurate diagnosis.
    • Scott Adams
      In this case the beer is excellent, but for those who are super sensitive it is likely better to go the full gluten-free beer route. Lakefront Brewery (another sponsor!) has good gluten-free beer made without any gluten ingredients.
    • trents
      Welcome to the forum, @catsrlife! Celiac disease can be diagnosed without committing to a full-blown "gluten challenge" if you get a skin biopsy done during an active outbreak of dermatitis herpetiformis, assuming that is what is causing the rash. There is no other known cause for dermatitis herpetiformis so it is definitive for celiac disease. You would need to find a dermatologist who is familiar with doing the biopsy correctly, however. The samples need to be taken next to the pustules, not on them . . . a mistake many dermatologists make when biopsying for dermatitis herpetiformis. 
×
×
  • 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.