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

Cross Contamination


HeatherMelissa

Recommended Posts

astyanax Rookie

i definitely understand the long term effects of consistently ingesting gluten (but thanks for the links! i should send those to my friends :) ) but what i'm confused about is the every little bit doing long term damage. for those of us who are pretty young that seems to spell out a future of being sick pretty much no matter how much you avoid gluten since inevitably you get sick (coincidentally i got sick today for the first time in a few months, even though i called a restaurant ahead of time, talked to a chef, and again at the restaurant specified that it was to be gluten free in preparation (it was gluten free as it appeared on the menu))

and that point someone else made, about some of us getting sick from something like lay's chips (even though now they have a separate line for a few) and some of us not and continuing to eat them. that would mean everyone was ingesting gluten from them (i actually did get sick and did avoid them but i used to eat them all the time)

i'm not advocating cheating, or being not strict, etc. i'm just starting to get afraid cos of course we all inevitably ingest a small amount. i always thought it was like ok i'll get sick here and there but as long as i'm strictly avoiding it overall i'm ok. now i'm scared because it's like if each little crumb does permanent damage, the younger you are the more sick you'll end up in the long run just by the inevitable ingestion of gluten over the years. and nevermind the huge issue of some people reacting to possible cross contamination - it makes even eating "gluten free" foods risky.

sorry i'm just confused :( and it seems what i was originally taught about celiac in my original diagnosis years ago was wrong !

as a side note too, i'm overall completely healthy. i even get sick less than my friends (i'm in school so everyone's always getting sick!) i don't have any other medical problems. and i want it to stay that way ! and i'm afraid that no matter how hard i try eventually, maybe not for 20 30 years but eventually i'm going to get those long term effects of celiac if every little bit of gluten is doing permanent damage to my system :(

thanks for help.


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



Celiac.com Sponsor (A8-M):



celiac3270 Collaborator

All of us make mistakes every now and then--but a mistake once in awhile won't do long-term damage. These symptoms apply to long-term gluten intake--like what we were all ingesting before diganosis. If you do make a rare mistake, it will not put you at risk for these symptoms--but constant mistakes could be a problem.

About the FritoLays, I think it comes down to opinion. Three products made by FritoLays are now made on dedicated lines according to a dietician from FritoLays. It basically comes down to whether you believe there's gluten in them--I don't get symptoms from them and my biopsy a few months ago showed no intestinal damage when I was consuming large amounts of their potato chips daily :), so I am not too concerned. It's up to you, though--just as it is up to you if you eat products that aren't made in a dedicated factory.

KaitiUSA Enthusiast

Yes there are four brands of Frito Lays that are on dedicated lines so if you have a reaction to those it would not be a gluten one. I have never even had a problem with their chips that have the risk for cross contamination. I also haven't had damage to my intestines or symptoms(and I am very sensitive) from them either so I am also not worried about that brand. I eat them all the time too and as celiac3270 said it comes down to your own opinion.

Also with the long term damage- that is for people who ignore the diet and continue to eat gluten constantly. That doesn't mean we should go out and gluten ourselves every now and then even if we don't have symptoms. It's never good to have mistakes but we all have them sometimes unfortunately.

Lynne Billington Newbie

You're all talking about 3 Lays chips that are made on dedicated lines, could you tell us what they are?

celiac3270 Collaborator

Four are, according to a FritoLays nutritionist: regular Lays, Ruffles, Fritos, and Lays Stax

KaitiUSA Enthusiast

Yep those that celiac3270 said are the ones that are made on a dedicated gluten-free line :D

tjack454 Newbie

I used to feel sick all the time. I was confused about my diet since I thought I had taken all the gluten out of it. I finally started a food diary. I list everything I eat every day and my reactions. I finally figured out that soy milk was the culprit for my stomach aches. I elimated it from my diet, and now feel much better. I don't know if this helps, but sometimes, especially when you are being so careful not to ingest gluten, you need to see if maybe you're reacting to something else.

Tammy


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



Celiac.com Sponsor (A8-M):



  • 3 months later...
Carriefaith Enthusiast

oooo I found it :D

You're all talking about 3 Lays chips that are made on dedicated lines, could you tell us what they are?

Four are, according to a FritoLays nutritionist: regular Lays, Ruffles, Fritos, and Lays Stax

celiac3270, do you know if all of these chips are produced on the same line? or are the regular Lays, Ruffles, Fritos on a separate line from the STAX?

celiac3270 Collaborator

I'm not sure...I just know that they're on dedicated gluten-free lines...I don't know if there could be issues with other allergens, if that's what you mean.

Carriefaith Enthusiast

Ok, thanks for your help :)

I don't know if there could be issues with other allergens, if that's what you mean.
Yeah, I'm just worried about dairy contamination, I have a bag of regular classic lays here in front of me... I think I'm going to try it :D
celiac3270 Collaborator

Ummm...okay. They're on the df list, I'm pretty sure--but like a lot of the things on the gluten-free list (with the exceptions of those four products), there is a chance of contamination, since they're not necessarily on dedicated lines.

Carriefaith Enthusiast

oh no. I didn't know the classic regular ones were different from the regular ones. Oh well, I'll just give them to someone else. Thanks for clearing that up B)

celiac3270 Collaborator

No, no...classic ones are regular ones. Just like regular Coke is called "Coca-Cola Classic." Baked are not dedicated, but the "classic" (regular) ones are made on dedicated lines.

Carriefaith Enthusiast

Well... I tried the plain ruffles ones and I think I answered my own question :lol: Yep... they must be on the same lines as chips with dairy on them. I had a dairy reaction after eating them :rolleyes: Ah Well... They weren't as good as I thought they would be, and I don't think I will be craving them again ;)

  • 2 weeks later...
gettingbetter Newbie

for Leidenschaft

The excess saliva and metallic taste might also be due to overdose of dietary nutrients such as Sodium iodine (Iodine): e.g., Open Original Shared Link states:

Hypersensitivity, or iodism, include metallic taste, increased salivation, burning or pain, coryza; swelling and inflammation of the throat. The eyes may be irritated and swollen. Pulmonary edema may develop. Acne skin eruptions or ioderma, gastro-intestinal upsets and diarrhea may also occur.

Another site that talks about it is:Open Original Shared Link

Hope you've found an answer by now or are feeling better.

I have a couple of questions. Has anyone been helped by cellular (vs. serum/blood) analysis of minerals? How about hair analysis? I have read that blood tests are pretty accurate with vitamin levels but as for the minerals, cellular levels may be very different than serum levels. I have muscle twitches all over and chronic constipation which are both helped a lot by high doses of magnesium supplements (the doctors say as long as your kidneys are functioning well that you will get rid of any extra from the supplements that your body doesn't need). However, my blood work has all said that my magnesium levels are actually slightly above normal. I sure would like to know what minerals I might need and how much.

I had severe iron deficient anemia which took 5 months to correct, and I am developing osteoporosis. I have borderline hyperthyroidism, although I have fatigue, cold intolerance and above normal weight. Geez this is all very confusing. Good luck all.

getting better

blood work and biopsy positive

gluten-free cf nut free since January 2005

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. - tiffanygosci replied to tiffanygosci's topic in Introduce Yourself / Share Stuff
      1

      Celiac support is hard to find

    2. - trents replied to mamaof7's topic in Parents, Friends and Loved Ones of Celiacs
      1

      Help understand results

    3. - mamaof7 posted a topic in Parents, Friends and Loved Ones of Celiacs
      1

      Help understand results

    4. - Dizzyma replied to Dizzyma's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      3

      Newly diagnosed mam to coeliac 11 year old

    5. - tiffanygosci posted a topic in Introduce Yourself / Share Stuff
      1

      Celiac support is hard to find

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

    • Total Members
      132,957
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • tiffanygosci
      EDIT: I did find a monthly Zoom meeting for Celiacs through the Celiac Disease Foundation, so I'll be able to talk with some other people on January 15. And I also found a Celiac Living podcast on Spotify made by a celiac. I feel a little bit better now and I am still hoping I will find some more personal connections in my area.
    • trents
      Welcome to the celiac.com community, @mamaof7! It means for the one celiac disease antibody test that was ordered, she tested negative. However, other tests should have been ordered, especially for someone so young who would have an immature immune system where there would be a high probability of being IGA deficient.  The one test that was ordered was an IGA-based antibody test. It is not the only IGA antibody test for celiac disease that can be run. The most common one ordered by physicians is the TTG-IGA. Whenever IGA antibody tests are ordered, a "total IGA" test should be included to check for IGA deficiency. In the case of IGA deficiency, all other IGA tests results will be inaccurate. There is another category of celiac disease antibody tests that can be used in the case of IGA deficiency. They are known as IGG tests. I will attach an article that gives an overview of celiac disease antibody tests. All this to say, I would not trust the results of the testing you have had done and I would not rule out your daughter having celiac disease. I would seek further testing at some point but it would require your daughter to have been eating normal amounts of gluten for weeks/months in order for the testing to be valid. It is also possible she does not have celiac disease (aka, "gluten intolerance") but that she has NCGS (Non Celiac Gluten Sensitivity, or just "gluten sensitivity" for short) which is more common. The difference is that celiac disease is an autoimmune disorder that damages the lining of the small bowel whereas NCGS does not autoimmune in nature and does not damage the lining of the small bowel, though the two conditions share many of the same symptoms. We have testing to diagnose celiac disease but there are no tests for NCGS. To arrive at a diagnosis of NCGS, celiac disease must first be ruled out. A gluten free diet is the solution to both maladies.   
    • mamaof7
      For reference, daughter is 18 mths old. Was having painful severe constipation with pale stool and blood also bloating (tight extended belly.) Liver and gallbladder are normal. Ultrasound was normal. Dr ordered celiac blood test. We took her off gluten after blood draw. She is sleeping better, no longer bloated and stools are still off color but not painful.    "GLIADIN (DEAMID) AB, IGA FLU Value  0.84 Reference Range: 0.00-4.99 No further celiac disease serology testing to be performed. INTERPRETIVE INFORMATION: Deamidated Gliadin Peptide (DGP) Ab, IgA A positive deamidated gliadin (DGP) IgA antibody result is associated with celiac disease but is not to be used as an initial screening test due to its low specificity and only occasional positivity in celiac disease patients who are negative for tissue transglutaminase (tTG) IgA antibody."   Anyone know what in the world this means. She isn't scheduled to see GI until late April. 
    • Dizzyma
      Hi Trent and Cristiana, thank you so much for taking the time out to reply to me.  My daughters GP requested bloods, they came back as showing a possibility of celiac disease, she advised me to continue feeding gluten as normal and wait on a hospital appointment. When we got that the doctor was quite annoyed that the gp hadn’t advised to go gluten free immediately as she explained that her numbers were so high that celiac disease was fairly evident. That doctor advised to switch to a gluten-free diet immediately which we did but she also got her bloods taken again that day as it made sense to double check considering she was maintaining a normal diet and they came back with a result of 128. The hospital doctor was so confident of celiac disease that she didn’t bother with any further testing. Cristiana, thank you for the information on the coeliac UK site however I am in the Rrpublic of Ireland so I’ll have to try to link in with supports there. I appreciate your replies I guess I’ll figure things as we go I just feel so bad for her, her skin is so sore around her mouth  and it looks bad at an age when looks are becoming important. Also her anxiety is affecting her sleep so I may have to look into some kind of therapy to help as I don’t think I am enough to help. thanks once again, it’s great to be able to reach out xx   
    • tiffanygosci
      I have been feeling so lonely in this celiac disease journey (which I've only been on for over 4 months). I have one friend who is celiac, and she has been a great help to me. I got diagnosed at the beginning of October 2025, so I got hit with all the major food holidays. I think I navigated them well, but I did make a couple mistakes along the way regarding CC. I have been Googling "celiac support groups" for the last couple days and there is nothing in the Northern Illinois area. I might reach out to my GI and dietician, who are through NW Medicine, to see if there are any groups near me. I cannot join any social media groups because I deleted my FB and IG last year and I have no desire to have them back (although I almost made a FB because I'm desperate to connect with more celiacs). I'm glad I have this forum. I am praying God will lead me to more people to relate to. In my opinion, celiac disease is like the only food- related autoimmune disease and it's so isolating. Thanks for walking alongside of me! I'm glad I know how to help my body but it's still not easy to deal with.
×
×
  • 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.