Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Is it Important to ONLY eat Certified gluten free?


Zenith

Recommended Posts

Scott Adams Grand Master

@MisterSeth,  Can I ask which chocolate bars you are referring to here?


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



Celiac.com Sponsor (A8-M):



MisterSeth Enthusiast
21 hours ago, Scott Adams said:

@MisterSeth,  Can I ask which chocolate bars you are referring to here?

walmart "great value" chocolate. some of them have "may contain barley". I was a little shaky about hershey, nestle, cadbury etc until I read that, I think barley is considered a common allergen in canada now.

Beverage Rising Star

I got badly glutened one time on Amy's gluten free lasagna.  Now I can't even look at any Amy's product without turning green.  I have only tried a few Saffron Road frozen items, and had no problems.  No problem with Udi's, I just don't like the taste.

Certified gluten free is safest, so if I am going to get a frozen item like that, then I try for certified.  I bought a bunch of Pyrex glass freezer containers and often when I made a good dinner, I'll make extra and make up a little frozen dinner that I can just pop in the microwave or oven for when I don't have time or energy to cook.

trents Grand Master

I've never had a problem with Amy's gluten-free frozen dinner products. Not sure if I have tried her lazagna, though. I mostly get the Asian dinners and sometimes the Mexican ones. I'm not a particularly sensitive celiac, however, so symptomatically I don't seem to react to minor CC. Thankfully, I don't have issues with soy and dairy like a lot of Celiacs.

Scott Adams Grand Master

I will say that if the Amy's product was labelled gluten-free, it likely is, but certainly there have been products labeled gluten-free that did contain gluten, and companies do occasionally have manufacturing problems. 

Amy's is a local company here in Santa Rosa, CA and they won't advertise on Celiac.com, at least according to someone I spoke with around 10 years ago, because of the many negative posts about their products regarding the possibility that they could contain gluten. At that time I invited them to get more involved in our forum and respond to those negative claims, but so far they've never done that. In the same conversation the ad manager told me that if I were to delete the negative posts they would advertise. I told them that we don't delete posts. It is a mystery to me why they would not want to respond here to customer complaints, or take such a position about advertising. They are still welcome to respond.

trents Grand Master

Scott,

I believe Amy's realizes that a lot of celiacs mistake being glutened with reactions to other ingredients or mistakenly identify a glutened event with a particular product when it was actually caused by gluten in another product they consumed around the same time. I'm guessing Amy's doesn't want to step into that quagmire on a forum, feeling they had more to lose than gain by doing so.

Heather Cardwell Newbie
On 3/16/2020 at 10:12 AM, Scott Adams said:

Newly diagnosed celiacs should keep a food diary and they may have to avoid other foods until they heal. Once they heal, which can take up to 2 years or more, they may be able to add back many foods that were causing them issues...except gluten of course.

Thank you for this information!  I'm newly diagnosed and once going gluten free I felt better for a couple of weeks but then most of my gut issues came back.  Getting discouraged. What do you recommend eating for the first year or so after diagnosis? 


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



Celiac.com Sponsor (A8-M):



Scott Adams Grand Master

I would avoid processed foods and try to stick with whole foods that you personally prepare. I’d avoid refined sugar as well. I had issues with corn, milk, tomatoes and chicken eggs for about two years after my diagnosis, and would swear back then that I’d gotten cross contamination with gluten until I realized that I had additional, temporary food intolerance.

Itnterestingly, the foods that I was most sensitive to were foods that I was told by my allergist years earlier that I had high allergic reactions to and should only eat 1-2 a week, which I ignored. I should probably be following that advice.

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now

  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      126,216
    • Most Online (within 30 mins)
      7,748

    cboling
    Newest Member
    cboling
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.9k
    • Total Posts
      69.2k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • knitty kitty
      @Milarynn,  Welcome to the forum!   Many undiagnosed, untreated Celiac Disease patients have vitamin and mineral deficiencies.  Be sure to have your Vitamin D level checked.  Vitamin D helps prevent bone loss, including loss from the jaw and teeth.   Magnesium and calcium are both important to bone health as well.  Magnesium helps keep the calcium from leaving your bones.  Magnesium helps make life sustaining enzymes with Thiamine Vitamin B1.  Low Magnesium and/or low Thiamine results in muscle cramping.   Thiamine deficiency is found in Pre-diabetes and Diabetes.  Poor absorption of the eight water soluble B vitamins and Vitamin C are found in Celiac Disease.  Insufficient Vitamin C can cause poor oral health, resulting in poor gum health such as receding and bleeding gums.  Vitamin C is needed to fight bacteria that cause plaque which causes cavities.  Vitamin C helps rebuild tooth enamel.   I've had jaw muscle cramping, TMJ problems, tooth loss and gum problems.  Do talk to your dentist about having Celiac Disease.  Practice good oral hygiene.  I'm also Diabetic and take Benfotiamine (a form of Thiamine) that helps regulate blood glucose and heal the intestines. Do keep us posted on your test results and your progress!
    • trents
      Milaryrnn, your post is confusing. First, your celiac disease antibody testing is negative. By any chance had you already been on a gluten free diet before the blood draw for these tests was done? That would result in negative antibody testing even if you had celiac disease. Or, had you previously been diagnosed with celiac disease and had the antibody testing done to check for compliance with the gluten free diet? Second, DNA testing cannot be used to confirm celiac disease. 40% of the general population has the genetic potential to develop active celiac disease but only about 1% of the population actually develops active celiac disease. It takes both the genetic potential and some triggering biological stress event in order to develop active celiac disease. Otherwise, the genes remain inactive. High lipase levels would indicate some problem with your pancreas. 
    • More2Learn
      Thanks, yes, I've gone back and forth.  There is a lot of autoimmune disease in my family, so primarily I was thinking a real diagnosis might be helpful for other family members -- especially as I have two young biological nephews.  I feel like I am at a crossroads, where if I'm going to test now would be the time, since I've been in a less-than-perfect eating period.  I'm either going to just going to use what I've learned in these last few months to purposely never cheat again (obviously there is the accidental glutening situations) or test first, and then do that.  I don't need an official diagnosis so much that if I'm doing well I'm going to sabotage that by then starting to eat gluten again. I'm so glad you said this.  Even from what I've read so far, it makes sense to me that this is a misconception.  But growing up with all kinds of allergies, I can see how, as for the general population it's just easier for everyone to simplify it down to a type of "allergy," people would assume this.  It's just how most people look at allergies and diets and gluten avoidance has been painted as both.  I even see it in my journey to date, when I say I want a gluten free selection at a restaurant and I am asked "is it an allergy?" and it is so much easier just to say yes (even if the answer is actually well, no, it's autoimmune).  Because the "yes" answer is the "this is serious" answer.
    • Milarynn
      Hello. I recently had an endo/colonoscopy and my GI Dr found lymphocytes in my stomach and small intestine. My TTG Ab, IgA was <2 (normal), GLIADIN (DEAMINATED) IGA at 5 (negative), and IgA at 237 (normal). However, a Lipase test revealed my levels were through the roof at 201, 3x above normal. My GI doctor ordered a dna test to confirm Celiac Disease. An A1C test was also done and I am pre-diabetic. When I got home from work today, I started to feel sever cramping in my jaw muscles. I started to have jaw muscle cramps in the the last year. Not to mention, even with good oral hygiene, I have rapidly developed periodontal disease. I did have a small amount of gluten, thinking it wouldn’t harm much but I was sadly mistaken. DNA results should be back in 2 weeks. 
    • kopiq
      I also have food particles left on toiet paper when i wipe and my stool is light yellow not absorbing fats. I urinate about 15 times a day and have very sticky snot,dry throat.
×
×
  • Create New...