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

Baked Lays Potato Chips - Are They Gluten Free?


Emilysmomma

Recommended Posts

Emilysmomma Rookie

Are Baked Lays potato chips gluten free? And what about the Baked Scoops? We eat those a lot in our house since I am on Weight Watchers, but my daughter was just recently diagnosed with Celiacs so I wanted to be sure she could have the Baked Lays products. Thanks!!!


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



Celiac.com Sponsor (A8-M):



dollamasgetceliac? Explorer
Are Baked Lays potato chips gluten free? And what about the Baked Scoops? We eat those a lot in our house since I am on Weight Watchers, but my daughter was just recently diagnosed with Celiacs so I wanted to be sure she could have the Baked Lays products. Thanks!!!

There is a lot of talk on the Forum about chips , I read that someone posted I can't find a chips that works. I have the same problem. So I suggest that you try Gluten Free Pretzil sticks from Glutino. They sell them on line I guess and at Whole Foods. They replace the craving for chips , and I have no trouble with them . Oh yeh they taste Good :D

home-based-mom Contributor
Are Baked Lays potato chips gluten free? And what about the Baked Scoops? We eat those a lot in our house since I am on Weight Watchers, but my daughter was just recently diagnosed with Celiacs so I wanted to be sure she could have the Baked Lays products. Thanks!!!

The only safe Lays chip is the original (not flavored) Stax. Everything else seems to be subject to cross-contamination. You might luck out and eat a bag or two without problems and then get really sick on the next one. Original Stax are produced on dedicated equipment.

GlutenGalAZ Enthusiast

Open Original Shared Link?

Above is the Frito Lay link -- the first question is about gluten. Look at the very bottom of the page:

*Our LAY

Lombardi25 Apprentice

I've been OK with their Wavy and Ruffles (don't know if this is luck or the cross-contamination is so slight that it doesn't bother me etc.), but I was eating Cheetos for about a week and I was so sick for that week, go figure. Ever since not eating Cheetos again I have felt great, so no more Cheetos for me. Just another one of those gotta try it and see how you do things I guess.

larry mac Enthusiast

In the year and a half since I've been diagnosed I haven't had a problem with any Frito Lay product. Of course I only eat the ones that don't contain wheat in the ingredients.

best regards, lm

Respira Apprentice

I make my own potato chips now, it's fairly simple to do and they taste better than any store bought chips


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



Celiac.com Sponsor (A8-M):



ksymonds84 Enthusiast
In the year and a half since I've been diagnosed I haven't had a problem with any Frito Lay product. Of course I only eat the ones that don't contain wheat in the ingredients.

best regards, lm

Me too. I practically live on the scoops with pace picante sauce. I am very sensitive and haven't had a problem but I only buy the scoops, stax, and sometimes the big frito's. For other chips, I haven't had a problem with the regular cape cod potato chips.

jparsick84 Rookie
The only safe Lays chip is the original (not flavored) Stax. Everything else seems to be subject to cross-contamination. You might luck out and eat a bag or two without problems and then get really sick on the next one. Original Stax are produced on dedicated equipment.

This is true. While I've never had a problem with the regular potato chips, Cheetos, or Fritos, I did buy a bag of Baked Lays the other day and got sick. When I finished the bag a week later (wanting to double check if that was it), I did have a reaction but only a weak reaction (i.e., just a few bumps on my elbow instead of bumps all over my feet and rump). So I don't know what that means, but if you're very sensitive, I wouldn't risk it.

Darn210 Enthusiast

We have followed the Frito-Lay list on their site (not just the Lays Stax) and have not had a problem so far (been over a year for us). For anyone who likes Cheetos, we have switched to Robert's Gourmet Tings. They are like Cheetos without the powdered cheese coating. They are run on a shared line, but the ingredient list is much shorter and does not include MSG. I have found them at Whole Foods and at Kroger.

Open Original Shared Link

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. - Iam replied to Larzipan's topic in Related Issues & Disorders
      33

      Has anyone had terrible TMJ/ Jaw Pain from undiagnosed Celiac?

    2. - trents replied to Scatterbrain's topic in Sports and Fitness
      6

      Feel like I’m starting over

    3. - bobadigilatis replied to Larzipan's topic in Related Issues & Disorders
      33

      Has anyone had terrible TMJ/ Jaw Pain from undiagnosed Celiac?

    4. - cristiana replied to Scatterbrain's topic in Sports and Fitness
      6

      Feel like I’m starting over


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,300
    • Most Online (within 30 mins)
      7,748

    Philbin
    Newest Member
    Philbin
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Iam
      Yes.  I have had the tmj condition for 40 years. My only help was strictly following celiac and also eliminating soy.  Numerous dental visits and several professionally made bite plates  did very little to help with symptoms
    • trents
      Cristiana makes a good point and it's something I've pointed out at different times on the forum. Not all of our ailments as those with celiac disease are necessarily tied to it. Sometimes we need to look outside the celiac box and remember we are mortal humans just like those without celiac disease.
    • bobadigilatis
      Also suffer badly with gluten and TMJD, cutting out gluten has been a game changer, seems to be micro amounts, much less than 20ppm.  Anyone else have issues with other food stuffs? Soy (tofu) and/or milk maybe causing TMJD flare-ups, any suggestions or ideas? --- I'm beginning to think it maybe crops that are grown or cured with glyphosphate. Oats, wheat, barley, soy, lentils, peas, chickpeas, rice, and buckwheat, almonds, apples, cherries, apricots, grapes, avocados, spinach, and pistachios.   
    • cristiana
      Hi @Scatterbrain Thank you for your reply.   Some of these things could be weaknesses, also triggered by stress, which perhaps have come about as the result of long-term deficiencies which can take a long time to correct.   Some could be completely unrelated. If it is of help, I'll tell you some of the things that started in the first year or two, following my diagnosis - I pinned everything on coeliac disease, but it turns out I wasn't always right!  Dizziness, lightheaded - I was eventually diagnosed with cervical dizziness (worth googling, could be your issue too, also if you have neck pain?)  A few months after diagnosis I put my neck out slightly carrying my seven-year-old above my head, and never assigned any relevance to it as the pain at the time was severe but so short-lived that I'd forgotten the connection. Jaw pain - stress. Tinnitus - I think stress, but perhaps exacerbated by iron/vitamin deficiencies. Painful ribs and sacroiliac joints - no idea, bloating made the pain worse. It got really bad but then got better. Irregular heart rate - could be a coincidence but my sister (not a coeliac) and I both developed this temporarily after our second Astra Zeneca covid jabs.   Subsequent Pfizer jabs didn't affect us. Brain fog - a big thing for people with certain autoimmune issues but in my case I think possibly worse when my iron or B12 are low, but I have no proof of this. Insomnia - stress, menopause. So basically, it isn't always gluten.  It might be worth having your vitamins and mineral levels checked, and if you have deficiencies speak to your Dr about how better to address them?    
    • knitty kitty
      @NanceK, I do have Hypersensitivity Type Four reaction to Sulfa drugs, a sulfa allergy.  Benfotiamine and other forms of Thiamine do not bother me at all.  There's sulfur in all kinds of Thiamine, yet our bodies must have it as an essential nutrient to make life sustaining enzymes.  The sulfur in thiamine is in a ring which does not trigger sulfa allergy like sulfites in a chain found in pharmaceuticals.  Doctors are not given sufficient education in nutrition (nor chemistry in this case).  I studied Nutrition before earning a degree in Microbiology.  I wanted to know what vitamins were doing inside the body.   Thiamine is safe and nontoxic even in high doses.   Not feeling well after starting Benfotiamine is normal.  It's called the "thiamine paradox" and is equivalent to an engine backfiring if it's not been cranked up for a while.  Mine went away in about three days.  I took a B Complex, magnesium and added molybdenum for a few weeks. It's important to add a B Complex with all eight essential B vitamins. Supplementing just one B vitamin can cause lows in some of the others and result in feeling worse, too.  Celiac Disease causes malabsorption of all the B vitamins, not just thiamine.  You need all eight.  Thiamine forms including Benfotiamine interact with each of the other B vitamins in some way.  It's important to add a magnesium glycinate or chelate supplement as well.  Forms of Thiamine including Benfotiamine need magnesium to make those life sustaining enzymes.  (Don't use magnesium oxide.  It's not absorbed well.  It pulls water into the intestines and is used to relieve constipation.)   Molybdenum is a trace mineral that helps the body utilize forms of Thiamine.   Molybdenum supplements are available over the counter.  It's not unusual to be low in molybdenum if low in thiamine.   I do hope you will add the necessary supplements and try Benfotiamine again. Science-y Explanation of Thiamine Paradox: https://hormonesmatter.com/paradoxical-reactions-with-ttfd-the-glutathione-connection/#google_vignette
×
×
  • 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.