Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Cross-Contamination Realities- Grits


Finally-45

Recommended Posts

Finally-45 Contributor

I've posted another question here,I'm basically just trying to figure out if I'm in the super sensitive Celiac category, should I act like one for a little while, or if I can relax since this is all so new to me.

I had grits this morning from a cafeteria and it occured to me I should see what the gluten-free community says about grits even though it's made from hominy. Most people seem to worry about cross-contamination.

I don't feel anything with the grits, but I did feel nauseated when I ate a cold cereal, which was listed less than 20ppm of gluten. I've had steel-cut oats, no problem. (I've avoided all other oats with little effort.) I felt sick from Chinese food, and decided to give it up. There is no doubt that I don't tolerate caramel color at all, even from a single cough drop.

The great thing is that I know what to look for now. Should I go to the paranoid level and try to eat all fresh foods that I prepare or are from a reputable gluten-free source?


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



Celiac.com Sponsor (A8-M):



T.H. Community Regular

It seems to be a matter of preference in the beginning. IMO, there's two ways you can go:

1. Go super gluten free from the beginning, eating only whole, fresh foods or reputable gluten free grains. Then when symptoms resolve, slowly add foods back in and see what you tolerate.

or

2. Go gluten free with whole foods and gluten free products, and then if things do not resolve, slowly take things out until you stop having reactions.

Right now, it sounds like you're probably following a slightly risky gluten free diet, not quite as gluten free as #2. Some examples.

Steel cut oats, if they aren't tested to be gluten-free, are a huge risk. They are almost always contaminated (to the point that scientists thought for a while that oats had some similar proteins to wheat, when it was just cross-contamination).

Chinese food (like fried rice) often has soy sauce added, and soy sauce has wheat as an ingredient. Unless you made it yourself with gluten-free soy sauce, of course.

Grits might be cc'd (many tolerate them fine) but if you didn't discuss your dietary needs with the chef at the cafeteria - avoiding gluten cross-contamination - then that's a more likely cause of gluten cc than the grits themselves.

So as to what to do, I guess I'd say you should decide what matters more, at this point. The diet challenges or the symptoms challenges. For me, the symptoms were so debilitating that the diet challenge of going super gluten free was better than living with the symptoms. My father was the opposite.

Skylark Collaborator

If you're in the US and don't tolerate carmel color, it's not a gluten issue. It's made from corn or the package has to declare wheat.

I agree with T.H. that you really don't quite have the diet right yet. You have to get certified gluten-free steel cut oats. Bob's Red Mill makes them. Chinese food is always a no-go. Even if you order a dish without the soy sauce (which is usually made from wheat and soy) it will be CC'd from the seasoned woks. I worry less about grits, although you can never be 100% sure about gluten CC with any grain.

I don't think eating fresh foods you prepare and sticking to tested gluten-free grains is "paranoid". I think that's the celiac diet. I rarely eat out, and if I do it's at a restaurant with a gluten-free menu. For bread, I buy brands like Rudi's and Udi's. I get my flours from Bob's Red Mill, who tests for gluten.

padma Newbie

I've posted another question here,I'm basically just trying to figure out if I'm in the super sensitive Celiac category, should I act like one for a little while, or if I can relax since this is all so new to me.

I had grits this morning from a cafeteria and it occured to me I should see what the gluten-free community says about grits even though it's made from hominy. Most people seem to worry about cross-contamination.

I don't feel anything with the grits, but I did feel nauseated when I ate a cold cereal, which was listed less than 20ppm of gluten. I've had steel-cut oats, no problem. (I've avoided all other oats with little effort.) I felt sick from Chinese food, and decided to give it up. There is no doubt that I don't tolerate caramel color at all, even from a single cough drop.

The great thing is that I know what to look for now. Should I go to the paranoid level and try to eat all fresh foods that I prepare or are from a reputable gluten-free source?

Chinese food has been off my list for a long time. Too risky. Even "wheat free" soy sauce usually has some wheat! Ugh!

Eating in a cafeteria that is not committed to be gluten free is dangerous. The chef can stir one pot of gluten with a spoon and use the same spoon in another "gluten free" pot.

The same goes for tortillas in Mexican food places. I ask them to use a clean pan to warm up the corn tortilla and NOT to put it on the stove where they warm up the flour tortillas.I ask them to wash their hands or change their gloves. I about drove a man crazy last weekend trying to explain what i needed. I didn't get sick, so he did a great job. I get so frustrated sometimes in ordering, especially if there is a language barrier, that I almost cry. I didn't use to persist because i was embarrassed, but not anymore.

The longer you are totally free of gluten the easier it will be for you to sort out where it is hiding. Also, as you find the other things you are allergic to, it will get easier.

Some candy is made on conveyor belts that have gluten on them and they don't have to list that because it is not an ingredient. I don't eat any candy except for dark chocolate without dairy or nuts made in a facility without gluten. I don't eat cough drops.

I got really tired of accidentally getting glutened by eating a product that wasn't really gluten free, so I'm rarely eating them anymore. My episodes of getting sick have diminished to an exposure only once in a very great while. My digestion is back to normal and no more pain. This site with everyone's helpful ideas is what got me over the hump. Good luck. You'll figure it out. Be patient with yourself.

Skylark Collaborator

Some candy is made on conveyor belts that have gluten on them and they don't have to list that because it is not an ingredient. I don't eat any candy except for dark chocolate without dairy or nuts made in a facility without gluten. I don't eat cough drops.

Can you substantiate this, please? I believe it's a rumor and no manufacturers have said anything about belts with gluten when we have written and asked about CC.

Finally-45 Contributor

Thanks, everyone. The caramel color is still an outstanding issue. There seems to be some disagreement, I just know that when I eat caramel color products, I get terrible indigestion and a swollen throat, so quickly that I could easily connect it to caramel color. But on the other hand, I do recall sometimes having a cola and not being bothered and just wondering if I was just having a "good" day.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      128,172
    • Most Online (within 30 mins)
      7,748

    Angie Helms
    Newest Member
    Angie Helms
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.1k
    • Total Posts
      70.7k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      For my first couple of years after discovering my celiac disease I also had to avoid cow's milk/casein and eggs, as well as other things, but could tolerate duck eggs and sheep and goat's milk products. I'm not sure if you've tried those, but it could be worth testing them out.
    • knitty kitty
      Hello, @Kwinkle, How are you doing?   Have you tried adding a Magnesium supplement?   The B Complex vitamins need magnesium to work properly, especially thiamine vitamin B 1.   Magnesium deficiency symptoms and Thiamine deficiency symptoms both include gas and bloating.  Thiamine deficiency symptoms also include loss of appetite and fatigue.   My gas and bloating resolved rather quickly when I took Benfotiamine (a form of thiamine shown to promote intestinal healing) and Magnesium Glycinate in addition to my B 50 Complex (all twice a day plus the following...).   I found Magnesium L-Threonate or Magnesium Taurate are better when taken with a form of thiamine called TTFD (Tetrahydrofurfuryl dusulfide) because all of these cross the blood brain barrier easily, which corrects the loss of appetite, fatigue and anxiety.    Like @Celiacandme said, keeping a food/mood/poo'd journal is a big help in finding problematic foods, and for making sure your diet is not carbohydrate heavy.  If you're eating a lot if processed gluten free facsimile foods, be aware they do not have vitamins and minerals added to them like their gluten containing counterparts.  For every 1000 kcal of carbohydrates, we need an extra 500 mg of thiamine to turn them into energy and not store them as fat.   Let us know how you're doing!
    • Scott Adams
      Yes, if you had symptoms when eating gluten ruling out celiac disease won't necessarily mean you'll be able to eat gluten again, although it might mean that you may be able to be less strict with your gluten-free diet. 
    • trents
      Have you considered the possibility that you might have NCGS (Non Celiac Gluten Sensitivity) rather than celiac disease? They share many of the same symptoms, the difference being that NCGS does not damage the lining of the small bowel. It is 10x more common than celiac disease. There is no test yet available for NCGS. Celiac disease must first be ruled out. In view of your genetic profile, I would give it consideration.
    • Kj44
×
×
  • Create New...