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.

  • 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. - MauraBue posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Have Tru Joy Sweets Choco Chews been discontinued??

    2. - catnapt replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      4

      how much gluten do I need to eat before blood tests?

    3. - suek54 replied to suek54's topic in Dermatitis Herpetiformis
      7

      Awaiting dermatitis herpetiformis confirmation following biopsy

    4. - knitty kitty replied to suek54's topic in Dermatitis Herpetiformis
      7

      Awaiting dermatitis herpetiformis confirmation following biopsy

    5. - suek54 replied to suek54's topic in Dermatitis Herpetiformis
      7

      Awaiting dermatitis herpetiformis confirmation following biopsy

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,260
    • Most Online (within 30 mins)
      7,748

    MauraBue
    Newest Member
    MauraBue
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • MauraBue
      Help!  My 5 year old daughter just stopped eating dairy and gluten due to her EoE and Celiac.  Her favorite candy in the world is tootsie rolls.  I did some research, and it sounds like these are the only options for finding something similar, but I can't find them anywhere to actually purchase.  Have they been discontinued??  Does anyone have another recommendation for a gluten-free/DF tootsie roll option?
    • catnapt
      I wonder how long it usually takes and if it is dose dependent as well... or if some ppl have a more pronounced reaction to gluten than others   thanks again for all the great info    
    • suek54
      Wow KK, thank you so much for all your attached info. I had a very quick scan but will read more in depth later.  The one concerning corticosteroid use is very interesting. That would relate to secondary adrenal insufficiency I think , ie AI caused by steroids such as taken long term for eg asthma. I have primary autoimmune AI, my adrenals are atrophied, no chance if recovery there. But I am in touch with some secondaries, so something to bear in mind. .  Niacin B3 Very interesting too. Must have a good read about that.  Im sure lots of questions will arise as I progress with dermatitis herpetiformis. In the mean time, thanks for your help.
    • knitty kitty
      Welcome to the forum, @suek54, I have Dermatitis Herpetiformis, too.  I found taking Niacin B3 very helpful in clearing my skin from blisters as well as improving the itchies-without-rash (peripheral neuropathy).  Niacin has been used since the 1950's to improve dermatitis herpetiformis.   I try to balance my iodine intake (which will cause flairs) with Selenium which improves thyroid function.   Interesting Reading: Dermatitis herpetiformis effectively treated with heparin, tetracycline and nicotinamide https://pubmed.ncbi.nlm.nih.gov/10844495/   Experience with selenium used to recover adrenocortical function in patients taking glucocorticosteroids long https://pubmed.ncbi.nlm.nih.gov/24437222/   Two Cases of Dermatitis Herpetiformis Successfully Treated with Tetracycline and Niacinamide https://pubmed.ncbi.nlm.nih.gov/30390734/   Steroid-Resistant Rash With Neuropsychiatric Deterioration and Weight Loss: A Modern-Day Case of Pellagra https://pmc.ncbi.nlm.nih.gov/articles/PMC12532421/#:~:text=Figure 2.,(right panel) upper limbs.&text=The distribution of the rash,patient's substantial response to treatment.   Nicotinic acid therapy of dermatitis herpetiformis (1950) https://pubmed.ncbi.nlm.nih.gov/15412276/
    • suek54
      Thank you all for your advice and the dermatitis herpetiformis article. The latter made me realise I had stopped taking my antihistamine, which I will restart today. The Dapsone has cleared the rash entirely but I still get quite a bit itching, absolutely nothing to see though. I know its notoriously hard to clear and its still relatively early days for me.  The iodine issue is very interesting. I do eat quite a bit of salt because I have Addison's disease and sodium retention is an issue. I also have autoimmune hypothyroidism, not sure how a low iodine diet would play into that? Because of my Addison's I am totally steroid dependent, I take steroids 4 x daily and cannot mount any defence against inflammation. I need to increase my meds for that. Now that I know what is wrong I can do just that if Im having a bad day. Life is very sweet, just so damn complicated sometimes! Hey ho, onwards. Thank you again for your advice.  
×
×
  • 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.