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

Lay's Kc Masterpiece Potato Chips


miles2go

Recommended Posts

miles2go Contributor

I am pretty sure, no almost positive, that I just got glutened by a small bag of these chips. I researched them on the web before buying them from the vending machine and read that they're processed on a line that's washed between products, so there's a risk for cc, but Lay's is touting them as gluten-free. I was a little dismayed to see that pesky "natural flavors" ingredient, but their claim is that these are gluten-free and I always thought they were a good company. I've never had any problem with the occasional Cheetos or plain Lay's urges, but I definitely won't by buying the KC masterpiece chips again.

They are going to do away with that natural flavors thing once the labeling laws go into effect in 2008, aren't they? Or am I just being optimistic? Seems that I read that somewhere.

Anyway, buyer beware! :(

Margaret


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



Celiac.com Sponsor (A8-M):



miles2go Contributor

I think I should have posted this to the ingredients list instead. Would a moderator mind moving it, if deemed appropriate?

Sorry!

Margaret

hez Enthusiast

There are several people on this board that have had cc issues with Frito-Lay products. I think your gut is your best guide, if they make you sick do not eat them again! I hope you feel better soon.

Hez

miles2go Contributor

Thanks, I've got the Pepto and am not at the point where I feel the need to reach for it, but...not buying those chips again!!

Margaret

lonewolf Collaborator

My son reacts to these - even before we knew he was gluten intolerant. I thought it was the large amount of MSG in them. I don't trust anything with that many ingredients in it.

CarlaB Enthusiast

It could be the long ingredient list causing the stomach upset. I don't do well with flavored chips, even ones I know are gluten-free (like Lays Stax, which are made in a gluten-free facility). For me, it's the flavoring, not the gluten. I just buy plain chips. :)

gdobson Explorer

Good advice. I wish I had read this a week ago, however, before my son and I both got sick on Lays Stacks Ranch flavored. That's what I get when I try to give him something a little different to jazz up his lunch. Now I'm back to not trusting products again.


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



Celiac.com Sponsor (A8-M):



lovegrov Collaborator

"Natural flavors" is not going away as an ingredient. However, you were most likely glutened by CC.

richard

num1habsfan Rising Star

I assume these are an american Lays chips? I've never heard of such a one in Canada..

~ lisa ~

DingoGirl Enthusiast

I never buy chips as am not allowed to have them in the house. Could EASILY eat a whole bag in one sitting. :ph34r: But, I do eat about 1/4 a bag of KC Masterpiece barbecue chips whenever I'm at my mom's (she is under strict instruction to take bag away from me after a certain amount), and have never had a problem.....and this is about the ONLY processed food I eat, other than occasional Hershey's or M&M's.

miles2go Contributor
I never buy chips as am not allowed to have them in the house. Could EASILY eat a whole bag in one sitting. :ph34r: But, I do eat about 1/4 a bag of KC Masterpiece barbecue chips whenever I'm at my mom's (she is under strict instruction to take bag away from me after a certain amount), and have never had a problem.....and this is about the ONLY processed food I eat, other than occasional Hershey's or M&M's.

One week later report: I'm fairly certain that I got glutened and probably from cc. The poops don't lie!!

I can't buy my own chips for the same reason that DingoGirl doesn't, the whole bag would be gone, even if I bought little bags and kept them at home...same for a box of Mary's Gone Crackers, they'd be gone inside a very short week. Yesterday I snarfed almost a whole box of Nut Thins. I eat very little processed food when I'm not like this, so I'll have to figure something out regarding the vending machine at work. If they had plain Lay's all the time, I'd be happy, but they faithfully stock Cheetos and hardly ever plain Lay's. And I'm allegedly allergic to corn via skin test, so probably shouldn't even be doing the Cheetos. Along with the most excellent idea that I read somewhere here about a fast-food place that is dedicated gluten-free, we need those dedicated gluten-free vending machines. Workers of the gluten-free world, unite! :D

Thanks for understanding, btw. ;)

I'm addicted to crunchy food. I eat a whole lot of veggies. Celery and carrots can only go so far...

JoeB Apprentice

I got glutened last month by Lay's Ruffles chips. The ingredients listed on the package were fine, so I assumed it was cc, too. I switched to Wise chips and haven't had any problems so far.

It is discouraging when you're so conscientious about reading ingreadients, but there's nothing you can really do except switch to another product.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,857
    • Most Online (within 30 mins)
      7,748

    LowellFrancis
    Newest Member
    LowellFrancis
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Rogol72
      Some interesting articles regarding the use of Zinc Carnosine to help heal gastric ulcers, gastritis and intestinal permeability. I would consult a medical professional about it's use. https://www.nature.com/articles/ncpgasthep0778 https://www.rupahealth.com/post/clinical-applications-of-zinc-carnosine---evidence-review https://pmc.ncbi.nlm.nih.gov/articles/PMC7146259/ https://www.fallbrookmedicalcenter.com/zinc-l-carnosine-benefits-dosage-and-safety/
    • Jillian83
      He is. Which makes everything even more difficult. I’m not a believer in “staying for the kids” but I have nowhere to go and it’s not just me, it’s me plus my babies. We live in a beautiful place, lots of land in the country and me and the kids love the place we’ve called home for their entire lives. But Im seeing that he’ll never change, that my kids deserve a happy healthy Momma, and that staying in this as is will be the early death of me. Then I look at the scars covering my entire body…this disease and the chronic stress I’ve been enduring for years that tell me I’m no longer beautiful and no one will ever look at me with interest again. I try self care, try to give myself grace so I can just start loving myself enough to gain strength but the slightest sparkle in my eye and skip in my step attracts his wrath and it all comes crashing ten fold. Life is just absolutely railing me from every single direction leaving me wanting to wave that white flag bc I don’t feel like there’s much hope no matter what happens. 
    • trents
    • Jillian83
      Hi, I was recently diagnosed with Celiac and dermatitis herpetiformis after years of suffering without answers. I lost my mind. I lost my job. I lost so much time. I lost Me. Conventional doctors are opulent come near me and the one who did sat across the room, misdiagnosed me, pumped me full of steroids which collapsed my entire hip for 6 months. So without answers I began my holistic journey. Fast forward a couple of years and still struggling with a mysterious whole body itchy, crawling “skin hell”, perfect teeth now deteriorating, thick hair now thinning rapidly and no more than a day or 2 at most relief….An acquaintance opened up a functional medicine practice. Cash only, I found a way. Within a month tests clearly showing my off the charts gluten allergy/sensitivity as well as the depletion of vital nutrients due to leaky gut and intestinal damage. dermatitis herpetiformis was more than likely what I was experiencing with my skin. I was happy. I thought this is easy, eat healthy Whole Foods, follow the diet restrictions and I finally get to heal and feel confident and like myself again very soon! 😔 Supplements are very pricey but I got them and began my healing. Which leads to the other major issue: not working, stay at home Mom of young kids, entirely financially dependent on my man of 7 plus years. He’s never been supportive of anything I’ve ever done or been thru. He controls everything. I’m not given much money ever at a time and when he does leave money it’s only enough to possibly get gas. His excuse is that I’ll spend it on other things. So my “allowance” is inconsistent and has conditions. He withholds money from me as punishment for anything he wants. Since being diagnosed, he’s gained a new control tactic to use as punishment. He now is in control of when I get to eat. He asked for proof of my diagnosis and diet bc he said I made it up just to be able to eat expensive organic foods. Then after I sent him my file from my doctor he then said she wasn’t a real doctor. 😡. I go days upon days starving, sometimes breaking down and eating things I shouldn’t bc I’m so sick then I pay horribly while he gets annoyed and angry bc I’m not keeping up with all the duties I’m supposed to be doing. His abuse turns full on when I’m down and it’s in these desperate times when I need his support and care the most that I’m punished with silence, being starved, ignored, belittled. He will create more of a mess just bc I’m unable to get up and clean so that when I am better, I’m so overwhelmed with chores to catch up that the stress causes me to go right back into a flare from hell and the cycle repeats. I’m punished for being sick. I’m belittled for starving and asking for healthy clean water. I’m purposely left out of his life. He won’t even tell me he’s going to the grocery or to get dinner bc he doesn’t want me to ask him for anything. I have no one. I have nothing. Im not better. My supplements ran out and I desperately need Vitamin D3 and a methylated B complex at the very minimal just to function….he stares at me blankly…no, a slight smirk, no words. He’s happiest when im miserable and I am miserable.  this is so long and im condensing as much as I can but this situation is so complicated and disgusting. And it’s currently my life. The “IT” girl, the healthy, beautiful, perfect skin, perfect teeth, thick and curly locks for days, creative and talented IT girl….now I won’t even leave this house bc Im ashamed of what this has dont to my body, my skin. Im disgusted. The stress is keeping me from healing and I think he knows that and that’s why he continues to keep me in that state. He doesn’t want me confident or successful. He doesn’t want me healed and healthy bc then how would he put the blame of all his problems on me? This journey has been hell and I’ve been in Hell before. I’ve been killed by an ex, I’ve been raped, robbed, held hostage, abused beyond nightmares but the cruelty I’ve experienced from him bc of this disease is the coldest I’ve ever experienced. I’ve wanted to give up. Starving and in tears, desperate…I found a local food pantry in our small town so I reached out just saying I had Celiac and was on hard times. This woman is blessing me daily with prepared gluten free meals, donations, educational info, people who know this disease and how they manage life and the blessings just keep coming. But it’s overwhelming and I feel like I don’t deserve it at all. He just glared and I know he’s going to sabotage it somehow. I don’t even know what to do anymore. I’m so broken and just want peace and healing. 
    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
×
×
  • 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.