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

Baffled By Little Caesars Pizza


Loch

Recommended Posts

Loch Newbie

I just signed up here because a questions be gnawing at me and I can't seem to find any answers. This seemed the best category to post under but if there is better please point me to it. I'm just a bit gluten sensitive while my mom has celiacs. She can have some pretty bad reactions within minutes of even small cross contamination. I'm not as strict with my diet as I should be and occasionally will eat quick food with gluten while out with friends.

From me straying from time to time I found that I never had any symptoms after eating Little Caesar Pizza. This was still shortly after my mom was diagnosed and I started to pay more attention to how I feel after I eat different food. So my mom, still dearly missing some gluteny foods, tried a slice after I told her how I thought it was odd as other pizza will wreak havoc on me. It's been awhile and we've return to that same Little Caesars multiple times and neither of us have had any noticeable problems from eating it.

My questions would be any ideas why something so obviously made with wheat, says so on their website, wouldn't give us problems(in my moms case acid reflex, nausea, fever, cramps, vomiting, and other intestinal distress), and can continuing to eat them still prove to be harmful?

TL:DR

Why would someone with celiac not be bothered by Little Caesars Pizza?

Can it still be harmful?


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



Celiac.com Sponsor (A8-M):



kwylee Apprentice

I have tested negative for Celiac as well, but I did test positive on another showing that my body was producing antibodies to gluten, which means that for years prior to my antibody test, my body would be on the defensive anytime I ingested gluten in any amount. I had become lightheaded all day every day, but gluten intolerance manifests in many ways and the symptoms can vary drastically one person to the next. Gluten can create systematic inflammation internally and lead to many diseases and autoimmune conditions too numerous to list here, not the least of which is Celiac, MS, Lupus, RA, diseases of the skin and thyroid, cancer, and in my case, attack of the brain and nervous system.

That slice of gluten filled pizza is doing harm to your mother's body, and if you feel like you are sensitive, chances are you could wind up like me as well. I ate it for 55 years before I found out what was making me dizzy and scared. Luckily, I found out in time to take it out of my diet and recover. But if people who are poisoned by gluten continue to ingest it, the outcome will not be as happy. Please consider all of this, especially the next time you let your mom take just one piece, it's just not worth it.

xjrosie Apprentice

My two daughters diagnosed with Celiac had no symptoms whatsoever. It just happened to show up on routine blood tests for my younger daughter who has diabetes. When they did the scope, it was severely affected by the gluten. So just because you don't feel anything doesn't mean it's not doing any harm.

I don't know what is in your area, but I'm sure there are other pizza places that could have gluten free offerings? Here in Michigan, we have Passport Pizza and Dan Good Pizza - both are knowledgeable about CC and Celiac too.

Korwyn Explorer

Do they have a sourdough crust? And if so is that the crust you are eating?

Takala Enthusiast

No, I looked up online what sort of crust they used and found a discussion forum of pizza makers talking about it, they use a high gluten flour, yeast, and a slow, cold rise:

Open Original Shared Link

Agree that both of them should knock it off with encouraging the other one the regular pizza consumption.

Loch Newbie

Thank you for the replies. I figured it could be harmful, at the least I knew it wasn't healthy. I should do more research. I really don't get the lack of symptoms for just one thing. I can't think of anything else I've eaten with gluten that I don't get sick on anymore.

It's really not a good reason but we are a busy and poorish family. Everything seems to make a steep jump in price if it has the words "Gluten Free" on them.

There are some local pizza places that offer gluten free pizza, but there seems to be little care or thought made to eliminated cross contamination. Getting sick on one places pizza. They said they only have one stove so that's where we figure the problem is. They say that it's more targeted at people making a dietary choice and not for people with an allergy. I've read that currently people can call their product gluten free even if there is a risk of cross contamination. While the other place it just of miserable quality.

sa1937 Community Regular

Loch, welcome to the forum! You definitely need to give up your Little Caesars pizza. Why don't you start making your own? It'll be so much better, not to mention safe, and it's really not that difficult. It just takes a little practice. Plus you can choose whatever toppings you like. Check out The Pizza Crust Thread to find lots of recipes. You could become the pizza-making expert in the family!!! biggrin.gif


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



Celiac.com Sponsor (A8-M):



GFinDC Veteran

Good idea SA. Loch, Kinickinick makes gluten-free pizza crusts. You can find them in the freezer section of stores.

sa1937 Community Regular

Good idea SA. Loch, Kinickinick makes gluten-free pizza crusts. You can find them in the freezer section of stores.

I bet homemade is even better!!! biggrin.gif

love2travel Mentor

I bet homemade is even better!!! biggrin.gif

I'm with you, Sylvia! FAR better. :D

sa1937 Community Regular

I'm with you, Sylvia! FAR better. :D

My son-in-law even makes gluten-free pizza as my daughter is also celiac. She says it's even better than the best gluten-free pizza they've had in Denver...and Denver is a gluten-free haven.

ndw3363 Contributor

I understand money is a problem that makes this diet difficult sometimes. That is why you have to learn to cook - I'm lucky in that I love to do it. But I know some people don't. Unfortunately, in order to have variety and a healthy diet, it's necessary at times. I hardly ever buy anything that is specifically labeled GLUTEN FREE. I buy chicken, pork, beef, frozen vegetables, rice, really good dark chocolate (my splurge), and other things. I found that I don't care for a lot of gluten free substitutes - so I just eat things that would naturally be gluten free anyway - that way I don't have to substitute. But boy do I miss pizza - so I do feel your pain. I slipped once...I was on vacation in FL in Nov, and someone ordered a pizza. I had at it. Felt great the whole rest of the trip. However about a week later, I was exhausted, short of breath, the tingling in my legs came back, my anxiety took over, and I didn't want to leave the house. So just because I didn't feel bad after I ate that pizza, doesn't mean that it didn't kick my butt for making a bad choice. Still a struggle to make smart choices every day (and I've been gluten-free for a year) - but one day at a time right? haha - spoken like true carbohydrate addict. :D

  • 7 months later...
dsbsnag Newbie

You've got to keep in mind that not all of your reactions are going to be physical. Trust me you are reacting to this -- whether you feel it or not. Do some googling on "silent celiac disease".

This gluten goes from the gut to your brain. It may not be manifesting itself physically; but, trust me it is neurologically.

ravenwoodglass Mentor

You've got to keep in mind that not all of your reactions are going to be physical. Trust me you are reacting to this -- whether you feel it or not. Do some googling on "silent celiac disease".

This gluten goes from the gut to your brain. It may not be manifesting itself physically; but, trust me it is neurologically.

Welcome to the board. Very wise words for a first post.

joelmw Rookie

You've got to keep in mind that not all of your reactions are going to be physical. Trust me you are reacting to this -- whether you feel it or not. Do some googling on "silent celiac disease".

This gluten goes from the gut to your brain. It may not be manifesting itself physically; but, trust me it is neurologically.

I just want to loudly second this.

I was diagnosed with celiac disease almost exactly a year ago. Frankly, since I've been gluten-free, I am not sure when I specifically get "glutened" but I can tell you for sure that the cumulative impact of gluten was devastating--extreme fatigue, brain fog, cramps--and quantifiable. I showed marked improvement within a couple of weeks and wouldn't dream of taking the chance that I'd go back to how I was feeling before changing my diet--not to mention the untold consequences that I didn't notice.

One of things that troubles me most on these forums is hearing folks suggest with confidence that a food isn't affecting them because they didn't have a noticeable physical reaction. I think it's kinda cool that they can sometimes be so sure, but extremely dangerous to assume that they will always know. There are just too many variables and our body's systems are too complex for me to take such claims seriously.

Gluten is poison. I'd no sooner eat something with gluten in it than chew on d-con or drink a cocktail made with paint thinner.

I agree that gluten-free often equals expensive, but I find that that's typically because folks are trying to eat "substitute" foods. I'm not gonna say I don't occasionally enjoy some gluten-free pizza, but for the most part I avoid grains altogether, concentrating on vegetables and meat. I know it's a personal thing, but I don't really miss the bread and can certainly live without doughy products.

  • 3 years later...
Genniegoose Newbie

This is so weird. I know this was posted years ago, but I am currently having the same fascinating non-reaction to Little Caesar's pizza. I've been gluten intolerant for about 5 years, non-celiac, but my symptoms are typically pretty intense. I had been on a very stable gluten free diet with no cheating for about 2 years when I finally had to cheat with Little Caesars pizza because it was the only food available in a situation I was stuck in.  Surprisingly I had no noticeable side effects. I waited 2 weeks to see if I felt anything, but I didn't. So I decided to try Little Caesar's again 1 week later and, again, no noticeable symptoms. So I decided to try a flour tortilla another week later, and BOOM, very bad stomach issues. So there is something strange about Little Caesar's pizza. My first guess is that the food quality is so poor and processed that my body can't even recognize the wheat/gluten. That wouldn't shock me. But I am curious about their recipe now.

But I do agree, even though I don't feel anything in my gut, it is still probably affecting me negatively in more subtle ways. I did notice I was more tired, sore and foggy-headed as of late.

  • 11 months later...
ECS Newbie

I just have sensitivity.  Although I rarely cheat, I noticed I don't always get symptoms (joint pain, migraines, fatigue, etc.) if I have been good at avoiding cross-contamination, have had plenty of sleep, and avoiding alcohol.  I think it might depend on how calm my immune system is.  Not worth the risk if you can avoid it though.  Just because you get away with it once doesn't mean it isn't a problem.  More recently I had Jimmy Johns catered food and was surprised I didn't have any symptoms the next day.  Normally fries cooked in a non-dedicated frier are enough to give me symptoms.

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Scott Adams replied to Jhona's topic in Introduce Yourself / Share Stuff
      35

      Does anyone here also have Afib

    2. - Jacki Espo replied to CDFAMILY's topic in Related Issues & Disorders
      5

      Covid caused reoccurrence of DH without eating gluten

    3. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      1

      New Celiac Mama in My 30s

    4. - Mari replied to Jmartes71's topic in Coping with Celiac Disease
      2

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,957
    • Most Online (within 30 mins)
      7,748

    Dogdad21
    Newest Member
    Dogdad21
    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

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • 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
×
×
  • 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.