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

How Much Can We Trust Food Manufacturers?


Seeking2012

Recommended Posts

Seeking2012 Contributor

Ok so lets say we read the ingredients list and we found no wheat, barley, or rye ingredients. Great. But we know that's not the end of the story.

 

So lets say we look for allergen information, and there is none. And again we know that our detective work isn't over.

 

So lets say we then call the food company at the number listed on their packaging and the customer service rep tells us over the phone that the food/ingredients are processed on gluten-free equipment and there is no cross-contamination.

 

Is our work now done; can we trust them? Does it end here? I say this is a Celiac who never has GI symptoms, so my gut isn't going to tattle on them.


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



Celiac.com Sponsor (A8-M):



w8in4dave Community Regular

I have never called a company. If I have problems with a product I just never buy it again. I actually only had problems with some rice once and then gave it away and now only buy gluten-free rice. I look on this site for good products. Tried and true stuff. I figure someone eles has already done the foot work why should I do it again? I trust everyone in here. 

LauraTX Rising Star

I feel your predicament, as I also have no telling GI symptoms.

 

In the end, there is a level of trust that you have to place in companies.  For me, I will spend the extra dollar on something that is made by a company who takes the time to give clear allergen information.  Certified gluten-free stuff is the way to go if you can, but once you get into more everyday products like pasta sauce, salad dressing, etc, it is important to me that I buy brands that are very gluten-free friendly with their labeling.  

 

If I have to go out of my way and contact a company to get allergen information, I will buy a clearly labeled/allergen info at the ready product instead of it, unless it is something exceptionally good.  I also shop at a grocery store who has the best gluten-free labeling on their private label products out of the 6 other grocery stores around me. Why work hard to seek out info when there is a clearly labeled choice... I choose to spend my money rewarding the companies who are clear about disclosing things in the first place.

 

I am also very anal retentive about making sure things are gluten-free because my body will not tell me if I get glutened.

cyclinglady Grand Master

I hear ya! But I have the best "gluten meter" -- my husband! One glutening and he is cranky and snores heavily that very day ( never snores otherwise!). Makes it easier to track down a gluten source which is almost ALWAYS from a restaurant. I can pretty much trust manufacturers.

Archived

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

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

    • Total Members
      133,073
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • Tazfromoz
      My understanding, and ex I erience is that we coeliacs are likely to suffer more extreme reactions from viruses. Eg we are more likely to be hospitalised with influenza. So, sadly, your shingles may be worse because you are coeliac. So sorry you had to go through this. My mother endured shingles multiple times. She was undiagnosed with coeliac disease until she was 65. Me at 45. I've had the new long lasting vaccine. It knocked me around badly, but worth it to avoid shingles.
    • hjayne19
      Hi all,  Looking for some advice. I started having some symptoms this past summer like night sweats and waking at 4 am and felt quite achy in my joints. I was training heavily for cycling for a few weeks prior to the onset of these symptoms starting. I have had low Ferratin for about 4 years (started at 6) and usually sits around 24 give or take. I was doing some research and questioned either or not I might have celiac disease (since I didn’t have any gastric symptoms really). My family doctor ran blood screening for celiac. And my results came back: Tissue Transglutaminase Ab IgA HI 66.6 U/mL Immunoglobulin IgA 1.73 g/ My doctor then diagnosed me with celiac and I have now been gluten free for 3 months. In this time I no longer get night sweats my joint pain is gone and I’m still having trouble sleeping but could very much be from anxiety. I was since referred to an endoscopy clinic to get a colonoscopy and they said I should be getting a biopsy done to confirm celiac. In this case I have to return to eating gluten for 4-6 weeks before the procedure. Just wanted some advice on this. I seem to be getting different answers from my family physician and from the GI doctor for a diagnosis.    Thanks,  
    • yellowstone
      Cold/flu or gluten poisoning? Hello. I've had another similar episode. I find it very difficult to differentiate between the symptoms of a cold or flu and those caused by gluten poisoning. In fact, I don't know if my current worsening is due to having eaten something that disagreed with me or if the cold I have has caused my body, which is hypersensitive, to produce symptoms similar to those of gluten poisoning.        
    • Churro
      I'm no longer dealing with constipation. I got my liver test last month and it was in normal range. Two years ago I did have a vitamin D deficiency but I'm know taking vitamin D3 pills. Last month I got my vitamin D checked and it was in normal range. I don't believe I've had my choline checked. However, I do drink almond milk eat Greek yogurt on a daily basis. 
    • Wheatwacked
      Non-Celiac Gluten Sensitivity (NCGS) can be associated with low ferritin and iron deficiency. Once Celiac Disease (1% of the population affected) has been ruled out by tests the next step is to check for Non Celiac Gluten Sensitivity (10% of the population affected) by eliminating gluten for a trial period, then re-introduce Gluten Challange. Have you been supplementing Iron? How are your liver enzymes? Low levels of ferritin indicate iron deficiency, while  59% transferrin saturation indicates high iron levels.  Possibly indicating Fatty Liver Disease.  Choline is crucial for liver health, and deficiency is a known trigger for Non-Alcoholic Fatty Liver.  Some experts say that less than 10% eat the the Food and Nutrition Board established Adequate Intake that are based on the prevention of liver damage. Severe constipation and hemorrhoids may be linked to a bile or choline deficiency.  "Ninety-five percent of phospholipids (PLs) in bile is secreted as phosphatidylcholine or lecithin."  Fatty acid composition of phospholipids in bile in man   Deficiency of these bile salts causes the bile to get thick. Some people with Celiac Disease are misdiagnosed with Gall Bladder bile issues.  Removal of the gallbladder provides only temporary relief. Whether or not celiac disease or NCGS are your issues you need to look at your vitamin D blood level.   
×
×
  • 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.