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

Are Places Like Panera & Chipotle Safe?


jasonD2

Recommended Posts

jasonD2 Experienced

Panera has gluten-free options and chipotle is all gluten free except for the tortillas but when those servers keep digging their hands thru all the ingredients to build a salad or a burrito bowl it gets me worried


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

Was just at Chipolte for my son who is not gluten-free. The guy who rolled the flour tortillas up, used his gloved hands to get the cheese. :angry:

GFreeMO Proficient

Was just at Chipolte for my son who is not gluten-free. The guy who rolled the flour tortillas up, used his gloved hands to get the cheese. :angry:

I got severe CC from the gloved hands that roll the tortillas and then tough the lettuce and cheese etc. at Chipotle the one time I ate there.

i-geek Rookie

That's why I don't eat at Chipotle any more. I have successfully eaten at Qdoba several times- I always get the naked burrito (aka burrito bowl). The ones I've been to use spoons or tongs to handle all of the food items which lessens the chance of CC.

BethJ Rookie

I skip the lettuce, cheese and anything else that isn't dished up with a spoon or tongs. The first time I went to Chipotle, I asked them to change gloves and they were very accommodating but usually it's so noisy in there it's just easier to do without than scream at them why I want them to change gloves. I still get very nervous watching them move my bowl along the line while they're handling all those giant flour tortillas.

Skylark Collaborator

Chipotle warms the corn tortillas on the same grill as the flour. That CC'd me once. :angry: I order the rice bowl now and avoid toppings they dish out with gloves and it works fine.

brendygirl Community Regular

I have to tell ya, I eat out 2-5x a week, and I never eat at Chipotle. I went in once, when my brother was being his selfish self (he is allergic to eggs, seeds, poultry, etc, so we can't go to a chicken place or a salad place, but we can go to places swimming in gluten) and when I saw how fast those people were slapping that stuff together, I saw contamination everywhere. And I'm usually the one who thinks people on here are overly worried about cc (like the people who put menus up like tents around their food when they eat to avoid airborne particles).

Plus, it was so loud in there, when I asked for a gluten free menu, just out of curiosity, the guy couldn't even hear what I was saying.

I went to have Panera's soup one day, and it was fine. But, I have a hard time watching people eat all those rolls and bread bowls and seeing all the beautiful displays of stuff I can't have, and even the big, celebratory stencils of wheat all over, that I just stay away.

I'd rather go somewhere where I can have the shrimp plate that other people are too cheap to spring for, and when they drool over my plate, I just say, when you pay $6 for a mini loaf of frozen bread, a little extra for shrimp isn't a big deal at all.

Or when I can dive into dessert at PF Changs while the others oogle me and I can say, well I barely eat any carbs, given that I don't eat much bread! :P

Or dig into a bacon burger and fries at Farmer boys and say, there's less guilt when it's wrapped in lettuce!


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



Celiac.com Sponsor (A8-M):



MelindaLee Contributor

I LOVE the orchard salad there right now. The cherry vinegrette is so worth seeing all those lovely baked items I can't eat! Mmmmm.....too bad it's almost midnight and they aren't open!

Edit: opppssss....at Panera!

Frances03 Enthusiast

I personally love Chipotle. I've been in to MANY different ones all over, and they ALWAYS change their gloves and all the utensils in the entire place as soon as I mention that we have a "gluten allergy". We always get the bowl. The ONLY thing in the entire place with gluten is the flour tortillas and I can't imagine gluten "FLYING" around in there from a freakin flour tortilla. People worry way too much. I am SO thankful for a place like that where my son and I can EAT, it really bothers me when people start ripping it up one side and down the other. If you dont trust it, fine, dont eat there. To have a restaurant where the ONLY ingredient with gluten is an already made tortilla, I think that's pretty nice. I love their chips, they are SAFE, and good luck finding safe tortilla chips in a restaurant! And don't eat the corn tortillas if you dont like that they warm them on the same machine as the flour! OR, better yet, ask them to warm yours between foil! I do it all the time and they never mind! Or, get the crunchy corn, they are really good too! As for the lettuce and cheese, you can skip it, or you can ask them to get you some from the back. Or you can try to imagine the miniscule amount of gluten that would get on lettuce or cheese from a hand that touched a flour tortilla, and then imagine that being ENOUGH gluten to actually make you sick, and then you can convince yourself that you are indeed sick, and then hey, stay home for a week if it makes you happy. PHEW! I just had a pregnancy moment, but oh well, someone has to stand up for the people that aren't paranoid and are just out here trying to make it in this gluten filled world, while still enjoying our lives!

lpellegr Collaborator

I personally love Chipotle. I've been in to MANY different ones all over, and they ALWAYS change their gloves and all the utensils in the entire place as soon as I mention that we have a "gluten allergy". We always get the bowl. The ONLY thing in the entire place with gluten is the flour tortillas and I can't imagine gluten "FLYING" around in there from a freakin flour tortilla. People worry way too much. I am SO thankful for a place like that where my son and I can EAT, it really bothers me when people start ripping it up one side and down the other. If you dont trust it, fine, dont eat there. To have a restaurant where the ONLY ingredient with gluten is an already made tortilla, I think that's pretty nice. I love their chips, they are SAFE, and good luck finding safe tortilla chips in a restaurant! And don't eat the corn tortillas if you dont like that they warm them on the same machine as the flour! OR, better yet, ask them to warm yours between foil! I do it all the time and they never mind! Or, get the crunchy corn, they are really good too! As for the lettuce and cheese, you can skip it, or you can ask them to get you some from the back. Or you can try to imagine the miniscule amount of gluten that would get on lettuce or cheese from a hand that touched a flour tortilla, and then imagine that being ENOUGH gluten to actually make you sick, and then you can convince yourself that you are indeed sick, and then hey, stay home for a week if it makes you happy. PHEW! I just had a pregnancy moment, but oh well, someone has to stand up for the people that aren't paranoid and are just out here trying to make it in this gluten filled world, while still enjoying our lives!

Wow. That was shockingly insensitive. If you can't imagine gluten "flying" around from a tortilla, or the amount of cross-contamination on a glove affecting the cheese and lettuce, then you lack imagination and experience. Good luck to you in your gluten-free life, because with this cavalier attitude you will surely someday hurt yourself or someone else.

i-geek Rookie

I personally love Chipotle. I've been in to MANY different ones all over, and they ALWAYS change their gloves and all the utensils in the entire place as soon as I mention that we have a "gluten allergy". We always get the bowl. The ONLY thing in the entire place with gluten is the flour tortillas and I can't imagine gluten "FLYING" around in there from a freakin flour tortilla. People worry way too much. I am SO thankful for a place like that where my son and I can EAT, it really bothers me when people start ripping it up one side and down the other. If you dont trust it, fine, dont eat there. To have a restaurant where the ONLY ingredient with gluten is an already made tortilla, I think that's pretty nice. I love their chips, they are SAFE, and good luck finding safe tortilla chips in a restaurant! And don't eat the corn tortillas if you dont like that they warm them on the same machine as the flour! OR, better yet, ask them to warm yours between foil! I do it all the time and they never mind! Or, get the crunchy corn, they are really good too! As for the lettuce and cheese, you can skip it, or you can ask them to get you some from the back. Or you can try to imagine the miniscule amount of gluten that would get on lettuce or cheese from a hand that touched a flour tortilla, and then imagine that being ENOUGH gluten to actually make you sick, and then you can convince yourself that you are indeed sick, and then hey, stay home for a week if it makes you happy. PHEW! I just had a pregnancy moment, but oh well, someone has to stand up for the people that aren't paranoid and are just out here trying to make it in this gluten filled world, while still enjoying our lives!

Someone asked for opinions. We gave them. It was not a personal attack on you, geez. Oh, and thanks for being so condescendingly insulting as to imply that people who complain of cross-contamination from the servers' gloves are imagining things. Gosh, that sounds like all the doctors who've told so many of us for years that our symptoms were "all in our heads", we're just "paranoid", and we have "IBS" and there's nothing they can do, or restaurant servers/family members who serve unsafe food because "just a little bit can't hurt". Would you give similar advice to someone with an anaphylactic wheat allergy?

  • 2 weeks later...
3Celiacs Newbie

Personally, I think all of the comments reflect the severity of each person's individual response to gluten. Just goes to show that we'll never really know until we walk in that person's shoes!

Salax Contributor

Personally, I think all of the comments reflect the severity of each person's individual response to gluten. Just goes to show that we'll never really know until we walk in that person's shoes!

I agree. I also try to read each post as informational, nothing personal. In fact to a degree, I do understand the comment about gluten flying through the air from flour tortillas or that being extreme or whatever. It all depends on personal experience and what you are comfortable eating or not eating. To each his own I say. B)

Besides, we as a celiac and gluten intolerant group get alot of people that give us guff for what we are or what we aren't eatting. So I think we of all people can understand when someone may not be as sensitive to CC as other and there is no concern about touching a flour tortillas and then touching a corn one. It is what it is. Only you are responsbile for your health no one else is. So don't worry about what other people are doing, just worry about your self. And of course children if they apply or the naughty hubby that tries to kiss you after drinking a beer. :D

On a personal note, I have never eaten at chipotle..I hate cilantro...So there :P

cyberprof Enthusiast

Chipotle warms the corn tortillas on the same grill as the flour. That CC'd me once. :angry: I order the rice bowl now and avoid toppings they dish out with gloves and it works fine.

I've never tried anything but the burrito bowl. I skip the lettuce, cheese and anything else that they use their hands on. (I did get glutened when I ordered the cheese first time there.) I also ask them to change their gloves and have never had even a dirty look - I say I'm "allergic" to wheat. And I ask - if they don't offer- the original person to take my order the whole way through the line. Over the past 3.5 years, I've never been glutened and I have eaten there ~30 times, all at different locations. Seattle, Federal Way, Portland OR, Chapel Hill NC, California etc.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,951
    • Most Online (within 30 mins)
      7,748

    SY8
    Newest Member
    SY8
    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

    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
    • DebJ14
×
×
  • 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.