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:
    Join eNewsletter
    Donate

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - catnapt replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      2

      how much gluten do I need to eat before blood tests?

    2. - trents replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      2

      how much gluten do I need to eat before blood tests?

    3. - catnapt posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      2

      how much gluten do I need to eat before blood tests?

    4. - trents replied to McKinleyWY's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      4

      Accuracy of testing concerns

    5. - Theresa2407 replied to chrish42's topic in Doctors
      4

      Doctors and Celiac.com

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

    • Total Members
      133,255
    • Most Online (within 30 mins)
      7,748

    Christie Fassel
    Newest Member
    Christie Fassel
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • catnapt
      thank you so much for your detailed and extremely helpful reply!! I can say with absolute certainty that the less gluten containing products I've eaten over the past several years, the better I've felt.   I wasn't avoiding gluten, I was avoiding refined grains (and most processed foods) as well as anything that made me feel bad when I ate it. It's the same reason I gave up dairy and eggs- they make me feel ill.  I do have a bit of a sugar addiction lol so a lot of times I wasn't sure if it was the refined grains that I was eating - or the sugar. So from time to time I might have a cookie or something but I've learned how to make wonderful cookies and golden brownies with BEANS!! and no refined sugar - I use date paste instead. Pizza made me so ill- but I thought it was probably the cheese. I gave up pizza and haven't missed it. the one time I tried a slice I felt so bad I knew I'd never touch it again. I stopped eating wheat pasta at least 3 yrs ago- just didn't feel well after eating it. I tried chick pea pasta and a few others and discovered I like the brown rice pasta. I still don't eat a lot of pasta but it's nice for a change when I want something easy. TBH over the years I've wondered sometimes if I might be gluten intolerant but really believed it was not possible for me to have celiac disease. NOW I need to know for sure- because I'm in the middle of a long process of trying to find out why I have a high parathyroid level (NOT the thyroid- but rather the 4 glands that control the calcium balance in your body) I have had a hard time getting my vit D level up, my serum calcium has run on the low side of normal for many years... and now I am losing calcium from my bones and excreting it in my urine (some sort of renal calcium leak) Also have a high ALP since 2014. And now rapidly worsening bone density.  I still do not have a firm diagnosis. Could be secondary HPT (but secondary to what? we need to know) It could be early primary HPT. I am spilling calcium in my urine but is that caused by the high parathyroid hormone or is it the reason my PTH is high>? there are multiple feedback loops for this condition.    so I will keep eating the bread and some wheat germ that does not seem to bother me too much (it hasn't got enough gluten to use just wheat germ)    but I'm curious- if you don't have a strong reaction to a product- like me and wheat germ- does that mean it's ok to eat or is it still causing harm even if you don't have any obvious symptoms? I guess what you are saying about silent celiac makes it likely that you can have no symptoms and still have the harm... but geez! you'd think they'd come up with a way to test for this that didn't require you to consume something that makes you sick! I worry about the complications I've been reading about- different kinds of cancers etc. also wondering- are there degrees of celiac disease?  is there any correlation between symptoms and the amnt of damage to your intestines? I also need a firm diagnosis because I have an identical twin sister ... so if I have celiac, she has it too- or at least the genetic make up for having it. I did have a VERY major stress to my body in 2014-2016 time frame .. lost 50lbs in a short period of time and had severe symptoms from acute protracted withdrawal off an SSRI drug (that I'd been given an unethically high dose of, by a dr who has since lost his license)  Going off the drug was a good thing and in many ways my health improved dramatically- just losing 50lbs was helpful but I also went  off almost a dozen different medications, totally changed my diet and have been doing pretty well except for the past 3-4 yrs when the symptoms related to the parathyroid issue cropped up. It is likely that I had low vit D for some time and that caused me a lot of symptoms. The endo now tells me that low vit D can be caused by celiac disease so I need to know for sure! thank you for all that great and useful information!!! 
    • trents
      Welcome, @catnapt! The most recent guidelines are the daily consumption of a minimum of 10g of gluten (about the amount found in 4-6 slices of wheat bread) for a minimum of two weeks. But if possible stretching that out even more would enhance the chances of getting valid test results. These guidelines are for those who have been eating gluten free for a significant amount of time. It's called the "gluten challenge".  Yes, you can develop celiac disease at any stage of life. There is a genetic component but also a stress trigger that is needed to activate the celiac genes. About 30-40% of the general population possesses the genetic potential to develop celiac disease but only about 1% of the general population actually develop celiac disease. For most with the potential, the triggering stress event doesn't happen. It can be many things but often it is a viral infection. Having said that, it is also the case that many, many people who eventually are diagnosed with celiac disease probably experienced the actual onset years before. Many celiacs are of the "silent" type, meaning that symptoms are largely missing or very minor and get overlooked until damage to the small bowel lining becomes advanced or they develop iron deficiency anemia or some other medical problem associated with celiac disease. Many, many are never diagnosed or are diagnosed later in life because they did not experience classic symptoms. And many physicians are only looking for classic symptoms. We now know that there are over 200 symptoms/medical problems associated with celiac disease but many docs are only looking for things like boating, gas, diarrhea. I certainly understand your concerns about not wanting to damage your body by taking on a gluten challenge. Your other option is to totally commit to gluten free eating and see if your symptoms improve. It can take two years or more for complete healing of the small bowel lining once going gluten free but usually people experience significant improvement well before then. If their is significant improvement in your symptoms when going seriously gluten free, then you likely have your answer. You would either have celiac disease or NCGS (Non Celiac Gluten Sensitivity).
    • catnapt
      after several years of issues with a para-gland issue, my endo has decided it's a good idea for me to be tested for celiac disease. I am 70 yrs old and stunned to learn that you can get celiac this late in life. I have just gradually stopped eating most foods that contain gluten over the past several years- they just make me feel ill- although I attributed it to other things like bread spiking blood sugar- or to the things I ate *with* the bread or crackers etc   I went to a party in Nov and ate a LOT of a vegan roast made with vital wheat gluten- as well as stuffing, rolls and pie crust... and OMG I was so sick! the pain, the bloating, the gas, the nausea... I didn't think it would ever end (but it did) and I was ready to go the ER but it finally subsided.   I mentioned this to my endo and now she wants me to be tested for celiac after 2 weeks of being on gluten foods. She has kind of flip flopped on how much gluten I should eat, telling me that if the symptoms are severe I can stop. I am eating 2-3 thin slices of bread per day (or english muffins) and wow- it does make me feel awful. But not as bad as when I ate that massive amnt of vital wheat gluten. so I will continue on if I have to... but what bothers me is - if it IS celiac, it seems stupid for lack of a better word, to intentionally cause more damage to my body... but I am also worried, on the other hand, that this is not a long enough challenge to make the blood work results valid.   can you give me any insight into this please?   thank you
    • trents
      The biopsy looks for damage to the mucosal lining of the small bowel from the inflammation caused by celiac disease when gluten is ingested. Once you remove gluten from the diet, inflammation subsides and the mucosal lining begins to heal. 
    • Theresa2407
      Our support groups in Iowa have tried for years to educate doctors and resource sites like this one.  We have held yearly conferences with continued education classes.   We have brought in Dr. Murray, Dr. Fasano, Dr. Green and Dr. elliott.  In those many years we may have had 2 doctors attend.  We sent them information, with no response.  I talked to my personal doctor and she said their training for Celiac was to show them a skinny man in boxer shorts and a huge stomach.  Saying if you see this, it is Celiac.  If it isn't in their playbook then they don't care.  Most call it an allergy with no mention of our immune system.  There is so much false information on the internet.  Then people don't understand why they can't get well and are acquiring more immune diseases. I mention this site to everyone.  Scott has working hard for the Celiac community.
×
×
  • 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.