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

General Mills, Corn Chex, Gluten-Free cereal


RadDecor

Recommended Posts

RadDecor Newbie

I hadn't purchased this cereal in a couple of years.  Bought my recent box three weeks ago.  I've been sick ever since w/ the usual Celiac symptoms.  I can't remember the last time I've had a Celiac event, and because of that haven't been on Celiac.com in awhile.  Should have checked here first before purchasing General Mills, gluten-free cereals, as other member comments suggest it is not a safe gluten-free product.  Buyer beware.  

GetImage.webp


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

I know many many Celiacs that eat Chex with no issues.  I love them.  Perhaps you have a problem with corn?  

RadDecor Newbie

I wouldn't have posted this comment without first checking w/ past members, and what they had to say about General Mills"gluten-free" cereals.  Am trying to forewarn others to use caution when purchasing these breakfast staples.  Numerous Celiac.com members, as well as myself are having problems w/ this brand being gluten-free (it has nothing to do w/ corn).  Just trying to save one person from the pain and bloating I've been experiencing daily for the past two weeks.    

kareng Grand Master
8 minutes ago, RadDecor said:

I wouldn't have posted this comment without first checking w/ past members, and what they had to say about General Mills"gluten-free" cereals.  Am trying to forewarn others to use caution when purchasing these breakfast staples.  Numerous Celiac.com members, as well as myself are having problems w/ this brand being gluten-free (it has nothing to do w/ corn).  Just trying to save one person from the pain and bloating I've been experiencing daily for the past two weeks.    

I think " numerous Celiac. Com members" enjoy and do well with Chex cereals.  

kareng Grand Master

I am curious - which past members do you keep in contact with?  Maybe we have some of the same friends.  I keep up with about 30 on Facebook.  I know some of them really like rice or corn Chex, some don't eat any cereal, and one just likes fruity kids stuff. Lol

cyclinglady Grand Master

I have to say that is is possible that you were glutened by this product.  ANYTHING is possible.  With any processed food, there is a risk of contamination, be it gluten, bacteria, etc.  Just look at all the food recalls  (thanks to the manufacturers who step up to the plate when they have made a mistake!).  However, we love the convience of prepared foods!   

For celiacs, there is always a risk of gluten exposure.  Life is full of risks and we must just learn how to minimize them.  The safest approach would be to grow and prepare all your own food, but that is not going to happen, especially for us city dwellers.    Fortunately, there are laws in place but they are not perfect.  Mistakes happen.  We celiacs and NCGI sufferers must continue to advocate for safe food and drug handling and proper labeling.   There is always room for improvement.  

As far as Chex cereal is concerned, I consumed lots of it the first year I was diagnosed and my gluten-free hubby still consumes it.  I gave up most grains only because they affect my blood sugar and I have steered my hubby away from it due to weight issues.  There are healthier choices!  ?   Celiac.com has plenty of old postings about this cereal, but let's face it, they are only opinions and not supported by scientific facts!  Sad, but true.  Another point is that even vets recommend slowly introducing new dog food when switching brands.  Maybe you had too much of a good thing!  

I do try to keep up with the safety of processed foods, because we travel and I want to purchase them.   So, I subscribed to Gluten Free Watchdog.  It is like Consumer Reports and they test foods that members question.  I looked up Chex and the rice cereal has been tested to be gluten free (test done in 2011).  The corn version was not tested, but I assume that it would be safe as well, since it is 1) a naturally gluten free product and 2) it was manufactured in the same facility with the Rice Chex.  Again, this is a processed product and any contamination  is possible, but my risk management  assessment assures me that this product is most likely gluten free.  

What is in recent question, by the gluten-free WatchDog and the Canadian Celiac Organization,  is the gluten-free oats produced by General Mills which has to do with sorting methods and questionable testing.  Personally, I would steer clear of all General Mills oat-containing products until this is resolved.  

I am sorry that you are ill.  I can understand your future avoidance of this product.  I have been in your shoes several times with various products.    But unless you have tested this product scientifically, I do not think you should make a claim that this product specifically made you ill.  I do not think it is fair to the manufacturer.  

I hope you feel better soon!  ?

 

mmarton Newbie

I tried this cereal twice about 12 months apart. Both times had a bad reaction, so will not be eating these again. Too bad, I really like them- just not worth it.


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



Celiac.com Sponsor (A8-M):



RadDecor Newbie

So sorry I took the time to forewarn other members there might be a problem w/ this product.  Mmarton, thank you for backing me up.  Gosh, forbid that everything is so politically correct these days.  My intent was not to discredit General Mills, but to bring awareness.

  • 3 weeks later...
psawyer Proficient

I eat Corn Chex frequently, and have never had a problem. Well, I do have a problem, actually. They are not sold here in Canada so I have to cross-border shop to get them. ;) 

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. - cristiana replied to Scatterbrain's topic in Sports and Fitness
      5

      Feel like I’m starting over

    2. - knitty kitty replied to Jmartes71's topic in Related Issues & Disorders
      8

      My only proof

    3. - Wheatwacked replied to Jmartes71's topic in Coping with Celiac Disease
      8

      Related issues

    4. - NanceK replied to Jmartes71's topic in Related Issues & Disorders
      8

      My only proof

    5. - Wheatwacked replied to Scatterbrain's topic in Sports and Fitness
      5

      Feel like I’m starting over


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,295
    • Most Online (within 30 mins)
      7,748

    LaniH
    Newest Member
    LaniH
    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

    • 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
    • Wheatwacked
      Your goal is not to be a good puppet, there is no gain in that. You might want to restart the ones that helped.  It sounds more like you are suffering from malnutrition.  Gluten free foods are not fortified with things like Thiamine (B1), vitamin D, Iodine, B1,2,3,5,6 and 12 as non-gluten free products are required to be. There is a Catch-22 here.  Malnutrition can cause SIBO, and SIBO can worsen malnutrition. Another possibility is side effects from any medication that are taking.  I was on Metformin 3 months before it turned me into a zombi.  I had crippling side effects from most of the BP meds tried on me, and Losartan has many of the side effects on me from my pre gluten free days. Because you have been gluten free, you can test and talk until you are blue in the face but all of your tests will be negative.  Without gluten, you will not create the antigen against gluten, no antigens to gluten, so no small intestine damage from the antigens.  You will need to do a gluten challange to test positive if you need an official diagnosis, and even then, no guaranty: 10 g of gluten per day for 6 weeks! Then a full panel of Celiac tests and biopsy. At a minimum consider vitamin D, Liquid Iodine (unless you have dermatitis herpetiformis and iodine exasperates the rash), and Liquid Geritol. Push for vitamin D testing and a consult with a nutritionist experienced with Celiack Disease.  Most blood tests don't indicate nutritional deficiencies.  Your thyroid tests can be perfect, yet not indicate iodine deficiency for example.  Thiamine   test fine, but not pick up on beriberi.  Vegans are often B12 deficient because meat, fish, poultry, eggs, and dairy are the primary souces of B12. Here is what I take daily.  10,000 IU vitamin D3 750 mg g a b a [   ] 200 mg CoQ10 [   ] 100 mg DHEA [   ] 250 mg thiamine B1 [   ] 100 mg of B2 [   ] 500 mg B5 pantothenic acid [   ] 100 mg B6 [   ] 1000 micrograms B12 n [   ] 500 mg vitamin c [   ] 500 mg taurine [   ] 200 mg selenium   
    • NanceK
      Hi…Just a note that if you have an allergy to sulfa it’s best not to take Benfotiamine. I bought a bottle and tried one without looking into it first and didn’t feel well.  I checked with my pharmacist and he said not to take it with a known sulfa allergy. I was really bummed because I thought it would help my energy level, but I was thankful I was given this info before taking more of it. 
    • Wheatwacked
      Hello @Scatterbrain, Are you getting enough vitamins and minerals.  Gluten free food is not fortified so you may be starting to run low on B vitamins and vitamin D.   By the way you should get your mom checked for celiac disease.  You got it from your mom or dad.  Some studies show that following a gluten-free diet can stabilize or improve symptoms of dementia.  I know that for the 63 years I was eating gluten I got dumber and dumber until I started GFD and vitamin replenishment and it began to reverse.  Thiamine can get used up in a week or two.  Symptoms can come and go with daily diet.  Symptoms of beriberi due to Thiamine deficiency.   Difficulty walking. Loss of feeling (sensation) in hands and feet. Loss of muscle function or paralysis of the lower legs. Mental confusion. Pain. Speech difficulties. Strange eye movements (nystagmus) Tingling. Any change in medications? Last March I had corotid artery surgery (90 % blockage), and I started taking Losartan for blood pressure, added to the Clonidine I was taking already.  I was not recovering well and many of my pre gluten free symptoms were back  I was getting worse.  At first I thought it was caused a reaction to the anesthesia from the surgery, but that should have improved after two weeks.  Doctor thought I was just being a wimp. After three months I talked to my doctor about a break from the Losartan to see if it was causing it. It had not made any difference in my bp.  Except for clonindine, all of the previous bp meds tried had not worked to lower bp and had crippling side effects. One, I could not stand up straight; one wobbly knees, another spayed feet.  Inguinal hernia from the Lisinopril cough.  Had I contiued on those, I was destined for a wheelchair or walker. She said the symptoms were not from Losartan so I continued taking it.  Two weeks later I did not have the strength in hips and thighs to get up from sitting on the floor (Help, I can't get up😨).  I stopped AMA (not recommended).  Without the Losartan, a) bp did not change, after the 72 hour withdrawal from Losartanon, on clonidine only and b) symptoms started going away.  Improvement started in 72 hours.  After six weeks they were gone and I am getting better.  
×
×
  • 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.