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

Trouble W/lay's Plain Chips?


horsefarmer4

Recommended Posts

horsefarmer4 Apprentice

HAS ANYONE HAD ANY REACTIONS TO LAY'S WAVY OR ORIGINAL? I'M TRYING TO PIN POINT WHERE I'VE BEEN GETTING GLUTEN-SLIGHTLY.

THANKS, TINA


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



Celiac.com Sponsor (A8-M):



darlindeb25 Collaborator

I never have, I have been gluten free for 7 1/2 years and have never had trouble with Lay's plain. Many members say the safe Lay's chips are only made in Plano, Texas, that is stated on the bag and I have noticed since then, any bag I ever have is from Plano Texas, so maybe that is why I have not been glutened by them. I have never seen any from anywhere else though, so I do not know how true this is either! You will receive many different answers, I'm sure.

ravenwoodglass Mentor

Sometimes I do, sometimes I don't. Because sometimes I do I avoid them as I don't like playing roulette.

Mom23boys Contributor

I have also always heard that the Plano plant products are the only safe ones. To my knowledge I have only seen the Plano products but googling made me think that there are more plants.

RiceGuy Collaborator

I never eat Lay's, so I can't speak from personal experience. However, I have read that Lay's are notorious for MSG in their products. My advice would be to select such products which list the ingredients as potatoes, oil, and salt, rather than a long list of weird things you cannot pronounce. If the plain chips are free of such additives, then it may be CC, or perhaps a sensitivity to potatoes, nightshades, or maybe the type of oil used.

blueeyedmanda Community Regular

I used them once, and didn't feel too great afterwards, it was not the full glutening feeling but it was like my stomach was a touchy. I never tried them again. Some members on here have problems others do not. It is hit or miss.

jerseyangel Proficient

My experience has been that of hit or miss, too. I avoid Lays--except the plain Stax.


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



Celiac.com Sponsor (A8-M):



TestyTommy Rookie

I've had problems with Lays; it took me months to figure it out, since the ingredients are just potatoes, oil and salt. Lays apparently has CC problems. I won't eat them.

(MSG is used in the flavored chips, not the plain ones).

krysmaralie Newbie

I have had problems with Lay's plain. Which is strange, because I know the ingredient list is only about 3 items long! I get strange cramps and gas so have to avoid them :(

AnneM Apprentice

I have never had any problems eating Lays plain chips. I read alot of things on these boards that people say bother them and the things they list never bother me i find it strange that it does some people and not others, i think it maybe other things than gluten that bothers them also, me...i have celiac, no other food allergies this maybe why.

It's reasonable to believe it's because of gluten or cc...but it could be something else. I haven't had a glutening in a long time, and i do eat alot of these foods people ask about. ..Quaker rice cakes..lays chips...amys...theres alot more i cant think of now. I know sometimes i just get a regular tummy ache..it isn't always gluten..but it is the first thing that comes to mind.

loco-ladi Contributor

Never looked to see what plant mine are manufactured in....

have a small issue but I think its more oil related than anything else as I also get the same thing when I make food at home I try only to eat a handful and have no problems however if I eat more, the problem increases. Wouldn't call it gluten symptoms but more of a gut ache??????

aikiducky Apprentice

People's sensitivity really can vary, some people will react to the tiniest amount of cc, others will need a bit more gluten before their immune system wakes up. That's why with some products it's a question of try it and see.

Pauliina

cruelshoes Enthusiast

We eat the Lays plain chips with probably too much regularity :lol: and we have never reacted to them. My son and I are very sensitive to the smallest amount of gluten, and our antibodies are in the negative range. While I don't disbelieve that some have CC experiences with them, that has never been our experience.

babygirl1234 Rookie

i never had a problem with lays plan chips

ginghamkim Apprentice

In the beginning after going gluten-free I did and sometimes I do now when I over indulge. Could it be the fat content? My understanding is that you digestive system has to work so much harder to digest fat b/c things are working right (is that technical enough---argh)

Anyway, do other high fat content thinks bother you?

larry mac Enthusiast

I don't eat the plain Lay's simply because I like the Ruffles better. Ruffles have ridges :rolleyes:. I also eat plain Fritos, Tostitos (for making nachos and dipping queso), and Cheetos. Haven't ever had a problem.

There's no MSG or preservatives in the Ruffles, Fritos, or Tostitos. Even if there was (which there is in the Cheeto Puffs), it doesn't bother me. MSG, preservatives, and those ingredients with the long names are not gluten. Maybe they're bad for you, maybe not. If they don't digest well for you, I certainly wouldn't eat them. Chips fried in oil with all that salt aren't exactly health food.

If I didn't have Celiac, I'd be eating a big 'ol greasy double cheeseburger. Or some pizza, fried chicken, fried fish, doughnuts, or any of many unhealthy foods. So please, leave me with some vestige of a vice so that I can thumb my nose at the universe and have my few guilty pleasures. :D

best regards, lm

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. - GlorietaKaro replied to GlorietaKaro's topic in Super Sensitive People
      3

      Am I nuts?

    2. - trents replied to GlorietaKaro's topic in Super Sensitive People
      3

      Am I nuts?

    3. - lalan45 replied to xxnonamexx's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      29

      My journey is it gluten or fiber?

    4. - Russ H posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      0

      Anti-endomysial Antibody (EMA) Testing

    5. - Scott Adams replied to JoJo0611's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      1

      Just diagnosed today

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

    • Total Members
      132,806
    • Most Online (within 30 mins)
      7,748

    IleneG
    Newest Member
    IleneG
    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

    • GlorietaKaro
      Thanks to both of you for your responses!  Sadly, even after several years of very strict gluten avoidance, I remember the symptoms well enough that I am too frightened to risk a gluten challenge— heartbeat and breathing problems are scary— Scott, thank you for the specific information— I will call around in the new year to see if I can find anyone. In the meantime, I will carry on has I have been— it’s working! Thanks also for the validation— sometimes I just feel crushed by disbelief. Not enough to make me eat gluten though—
    • trents
      Welcome to the celiac.com community, @GlorietaKaro! As Scott indicated, without formal testing for celiac disease, which would require you to have been consuming generous amounts of gluten daily for weeks, it would be not be possible to distinguish whether you have celiac disease or NCGS (Non Celiac Gluten Sensitivity). Their symptoms overlap. The difference being that celiac disease is an autoimmune disorder that damages the lining of the small bowel. We actually no more about celiac disease than we do about NCGS, the mechanism of the latter being more difficult to classify. There are specific antibody tests for celiac disease diagnosis and there is also the endoscopy/biopsy of the small bowel lining. Currently, there are no tests to diagnose NCGS. Celiac disease must first ruled out. Researchers are working on developing testing methods to diagnose celiac disease that do not require a "gluten challenge" which is just out of the question for so many because it poses serious, even life-threatening, health risks. But we aren't there yet.
    • lalan45
      That’s really frustrating, I’m sorry you went through that. High fiber can definitely cause sudden stomach issues, especially if your body isn’t used to it yet, but accidental gluten exposure can feel similar. Keeping a simple food/symptom journal and introducing new foods one at a time can really help you spot patterns. You’re already doing the right things with cleaning and separating baking—also watch shared toasters, cutting boards, and labels like “may contain.”
    • Russ H
      I thought this might be of interest regarding anti-EMA testing. Some labs use donated umbilical cord instead of monkey oesophagus. Some labs just provide a +ve/-ve test result but others provide a grade by testing progressively diluted blood sample. https://www.aesku.com/index.php/ifu-download/1367-ema-instruction-manual-en-1/file Fluorescence-labelled anti-tTG2 autoantibodies bind to endomysium (the thin layer around muscle fibres) forming a characteristic honeycomb pattern under the microscope - this is highly specific to coeliac disease. The binding site is extracellular tTG2 bound to fibronectin and collagen. Human or monkey derived endomysium is necessary because tTG2 from other mammals does not provide the right binding epitope. https://www.mdpi.com/1422-0067/26/3/1012
    • Scott Adams
      First, please know that receiving two diagnoses at once, especially one you've never heard of, is undoubtedly overwhelming. You are not alone in this. Your understanding is correct: both celiac disease and Mesenteric Panniculitis (MP) are considered to have autoimmune components. While having both is not extremely common, they can co-occur, as chronic inflammation from one autoimmune condition can sometimes be linked to or trigger other inflammatory responses in the body. MP, which involves inflammation of the fat tissue in the mesentery (the membrane that holds your intestines in place), is often discovered incidentally on scans, exactly as in your case. The fact that your medical team is already planning follow-up with a DEXA scan (to check bone density, common after a celiac diagnosis) and a repeat CT is a very proactive and prudent approach to monitoring your health. Many find that adhering strictly to the gluten-free diet for celiac disease helps manage overall inflammation, which may positively impact MP over time. It's completely normal to feel uncertain right now. Your next steps are to take this one day at a time, focus on the gluten-free diet as your primary treatment for celiac, and use your upcoming appointments to ask all your questions about MP and what the monitoring plan entails. This dual diagnosis is a lot to process, but it is also the starting point for a managed path forward to better health. This article has some detailed information on how to be 100% gluten-free, so it may be helpful (be sure to also read the comments section.):    
×
×
  • 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.