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Kellogs Corn Flakes


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does anyone know if we can have them? they are not labeled with anything so i was just wandering.

Lauren


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Ursa Major Collaborator

I believe I have read that they're sweetened with barley malt. Somebody correct me if I'm wrong, please. If I'm right, then they contain gluten.

CarlaB Enthusiast

I thought all Kellogg's products were a no-no.

flagbabyds Collaborator

they are not gluten-free they do have barley malt in them

sorry :(

Guest CD_Surviver

well since we cant have them has anyone found a good substitute? i have this really good recipe for potatoes that you coat in corn flakes.

Gluten Slayer Rookie

EnviroKidz Organic Amazon frosted flakes cereal. It tastes likes Kelloggs, very good.

Luvs to Scrap Apprentice

Natures Path Corn Flakes which are lightly sweetened with fruit juice are good too. My guys are gluten-free, not me, and I think they taste normal and use them in all my recipes that call for cornflakes. :) Kendra


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KaitiUSA Enthusiast

Kelloggs is not ok but I like Envirokidz brand

  • 1 year later...
mattj Rookie

At a celiac's meeting the experts (A doctor, nurse and dietician) said that Kelloggs Cornflakes and Rice Krispies are now considered gluten free. I haven't been able to find the confirmation I need before going ahead and eating them.

Does anyone know?

happygirl Collaborator

Question:

Do you have any gluten-free products?

Answer:

At this time, we do not offer products suitable for consumers on a gluten-free diet except as follows:

Kellogg's

blueeyedmanda Community Regular

There is Barley Malt in them....

If you have a Wegmans near you, they have Strawberry Corn Flakes under their own label, you find it in the Organic Section. It is organic. I have had it and it is very good. It is labeled gluten free too.

larry mac Enthusiast
does anyone know if we can have them? they are not labeled with anything so i was just wandering.

Lauren

Except if you consider barley malt flavoring a gluten ingredient.

I've tried every "health food" gluten free corn flakes I could get my hands on. They all suck if you ask me. Hard, not light and crispy like they are supposed to be. Sorry, I once worked for Frito Lay Research and conducted blind taste panel product testings. I tend to be very critical. You may find them acceptable. Please post your impressions.

best regards, lm

ravenwoodglass Mentor
At a celiac's meeting the experts (A doctor, nurse and dietician) said that Kelloggs Cornflakes and Rice Krispies are now considered gluten free. I haven't been able to find the confirmation I need before going ahead and eating them.

Does anyone know?

With the government deciding how much poison we could have I am not surprised about this at all. They are not gluten free. Period. If an item contains wheat starch or barley malt it is not gluten-free. It just tests below the level that has been determined to be okay to poison us with. As expected when the determination was made by the FDA we now can't even trust that a phone call to a rep or gluten free label means gluten free, we have to decide if it is gluten free by nature or by testing. I wonder why thats okay with gluten and not with peanuts. Oh wait a minute I know why, peanuts kill those reactive to them immediately, when they give us gluten it kills us slowly and makes for lots of money for the doctors while we try to figure out what else could be wrong with us cause we are eating labeled 'gluten free' food and still sick.

dadoffiveboys Rookie
At a celiac's meeting the experts (A doctor, nurse and dietician) said that Kelloggs Cornflakes and Rice Krispies are now considered gluten free. I haven't been able to find the confirmation I need before going ahead and eating them.

Does anyone know?

First.. don't ever assume a doctors 'recommended' list is correct. I've helped to correct some doctor's lists on gluten-free. The latest was from the children's feeding clinic program (for my child with celiac (but not diagnosed by a doctor - won't get into why)) and they had on their list McCann's Irish Oats. If you do research, you will find that SOME batches of their oats test with no trace of gluten.. but others have tested with over 300 ppm gluten (which under the new laws would NOT be gluten-free!). They supposedly changed mills and work really hard to be gluten-free but they are Gluten lite and you can't reliably eat them. I am VERY sensitive to gluten and trying the oats gave me a severe reaction - but it WAS on the gluten-free list by a specialty feeding program... just goes to show you that you must research every food and check. The only oats I've found to be free of gluten are the ones produced in Wyoming that I order via the internet (can't remember the company now..) We usually order a very large case each time and use them for oatmeal cookies and such. Being able to eat gluten-free oatmeal is GREAT for deserts.

  • 1 year later...
dermotron Newbie

I've recently stopped eating Kellogg's as I couldnt pinpoint what was getting gluten into my system. It appears Ive found the answer. The warning 'contains Barley' should have been enough I guess. There possibly listed as having no gluten due there being less than 10mg of gluten in them but thats too much for me. Fruit and yogurt is now the new morning cereal

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    • marion wheaton
      Thanks for responding. I researched further and Lindt Lindor chocolate balls do contain barely malt powder which contains gluten. I was surprised at all of the conflicting information I found when I checked online.
    • trents
      @BlessedinBoston, it is possible that in Canada the product in question is formulated differently than in the USA or at least processed in in a facility that precludes cross contamination. I assume from your user name that you are in the USA. And it is also possible that the product meets the FDA requirement of not more than 20ppm of gluten but you are a super sensitive celiac for whom that standard is insufficient. 
    • BlessedinBoston
      No,Lindt is not gluten free no matter what they say on their website. I found out the hard way when I was newly diagnosed in 2000. At that time the Lindt truffles were just becoming popular and were only sold in small specialty shops at the mall. You couldn't buy them in any stores like today and I was obsessed with them 😁. Took me a while to get around to checking them and was heartbroken when I saw they were absolutely not gluten free 😔. Felt the same when I realized Twizzlers weren't either. Took me a while to get my diet on order after being diagnosed. I was diagnosed with small bowel non Hodgkins lymphoma at the same time. So it was a very stressful time to say the least. Hope this helps 😁.
    • knitty kitty
      @Jmartes71, I understand your frustration and anger.  I've been in a similar situation where no doctor took me seriously, accused me of making things up, and eventually sent me home to suffer alone.   My doctors did not recognize nutritional deficiencies.  Doctors are trained in medical learning institutions that are funded by pharmaceutical companies.  They are taught which medications cover up which symptoms.  Doctors are required to take twenty  hours of nutritional education in seven years of medical training.  (They can earn nine hours in Nutrition by taking a three day weekend seminar.)  They are taught nutritional deficiencies are passe' and don't happen in our well fed Western society any more.  In Celiac Disease, the autoimmune response and inflammation affects the absorption of ALL the essential vitamins and minerals.  Correcting nutritional deficiencies caused by malabsorption is essential!  I begged my doctor to check my Vitamin D level, which he did only after making sure my insurance would cover it.  When my Vitamin D came back extremely low, my doctor was very surprised, but refused to test for further nutritional deficiencies because he "couldn't make money prescribing vitamins.". I believe it was beyond his knowledge, so he blamed me for making stuff up, and stormed out of the exam room.  I had studied Nutrition before earning a degree in Microbiology.  I switched because I was curious what vitamins from our food were doing in our bodies.  Vitamins are substances that our bodies cannot manufacture, so we must ingest them every day.  Without them, our bodies cannot manufacture life sustaining enzymes and we sicken and die.   At home alone, I could feel myself dying.  It's an unnerving feeling, to say the least, and, so, with nothing left to lose, I relied in my education in nutrition.  My symptoms of Thiamine deficiency were the worst, so I began taking high dose Thiamine.  I had health improvement within an hour.  It was magical.  I continued taking high dose thiamine with a B Complex, magnesium. and other essential nutrients.  The health improvements continued for months.  High doses of thiamine are required to correct a thiamine deficiency because thiamine affects every cell and mitochondria in our bodies.    A twenty percent increase in dietary thiamine causes an eighty percent increase in brain function.  The cerebellum of the brain is most affected.  The cerebellum controls things we don't have to consciously have to think about, like digestion, balance, breathing, blood pressure, heart rate, hormone regulation, and many more.  Thiamine is absorbed from the digestive tract and sent to the most important organs like the brain and the heart.  This leaves the digestive tract depleted of Thiamine and symptoms of Gastrointestinal Beriberi, a thiamine deficiency localized in the digestive system, begin to appear.  Symptoms of Gastrointestinal Beriberi include anxiety, depression, chronic fatigue, headaches, Gerd, acid reflux, gas, slow stomach emptying, gastroparesis, bloating, diarrhea and/or constipation, incontinence, abdominal pain, IBS,  SIBO, POTS, high blood pressure, heart rate changes like tachycardia, difficulty swallowing, Barrett's Esophagus, peripheral neuropathy, and more. Doctors are only taught about thiamine deficiency in alcoholism and look for the classic triad of symptoms (changes in gait, mental function, and nystagmus) but fail to realize that gastrointestinal symptoms can precede these symptoms by months.  All three classic triad of symptoms only appear in fifteen percent of patients, with most patients being diagnosed with thiamine deficiency post mortem.  I had all three but swore I didn't drink, so I was dismissed as "crazy" and sent home to die basically.   Yes, I understand how frustrating no answers from doctors can be.  I took OTC Thiamine Hydrochloride, and later thiamine in the forms TTFD (tetrahydrofurfuryl disulfide) and Benfotiamine to correct my thiamine deficiency.  I also took magnesium, needed by thiamine to make those life sustaining enzymes.  Thiamine interacts with each of the other B vitamins, so the other B vitamins must be supplemented as well.  Thiamine is safe and nontoxic even in high doses.   A doctor can administer high dose thiamine by IV along with the other B vitamins.  Again, Thiamine is safe and nontoxic even in high doses.  Thiamine should be given if only to rule Gastrointestinal Beriberi out as a cause of your symptoms.  If no improvement, no harm is done. Share the following link with your doctors.  Section Three is especially informative.  They need to be expand their knowledge about Thiamine and nutrition in Celiac Disease.  Ask for an Erythrocyte Transketolace Activity test for thiamine deficiency.  This test is more reliable than a blood test. Thiamine, gastrointestinal beriberi and acetylcholine signaling.  https://pmc.ncbi.nlm.nih.gov/articles/PMC12014454/ Best wishes!
    • Jmartes71
      I have been diagnosed with celiac in 1994, in remission not eating wheat and other foods not to consume  my household eats wheat.I have diagnosed sibo, hernia ibs, high blood pressure, menopause, chronic fatigue just to name a few oh yes and Barrett's esophagus which i forgot, I currently have bumps in back of my throat, one Dr stated we all have bumps in the back of our throat.Im in pain.Standford specialist really dismissed me and now im really in limbo and trying to get properly cared for.I found a new gi and new pcp but its still a mess and medical is making it look like im a disability chaser when Im actively not well I look and feel horrible and its adding anxiety and depression more so.Im angery my condition is affecting me and its being down played 
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