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

Something I Find Annoying


tennisman

Recommended Posts

tennisman Contributor

Recently I have been getting very annoyed at food companies . Why can't all food companies put Gluten Free or Not Gluten Free on their labels ? I mean it's very simple all it takes is 10 letters it's not difficult :angry: . Could you imagine how easy it would be to go shopping and find out if an item of food is Gluten Free or not in 1 second without having to read every single ingredient.

I am going to write a letter to some big food companies , and include videos or websites about Celiac Disease and ask them if it will be possible to start labelling more products with Gluten Free or not Gluten Free :) I mean they can write suitable for vegetarians so why can't they write Gluten Free on the labels ?????

Has anyone else written to food companies asking them to label more products ?


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



Celiac.com Sponsor (A8-M):



celiac-mommy Collaborator

I haven't, but I've called companies to thank them for their labeling or reformulating!

GlutenFreeManna Rising Star

I think some companies don't want to do it because of liability reasons. No gluten ingredients used does not always mean gluten free. Also in some countries if they claim something is gluten free they have to do testing to back up that claim. The US doesn't currently require testing, but I know other places do.

I get around this by just eating mostly whole unprocessed foods that are naturally gluten free. There's no need to pick up a bunch of bananas and try to figure out if it has gluten in it. ;)

jenngolightly Contributor

I also think they don't do it for commercial reasons. People are wary of "gluten free." Don't you have relatives who turn up their noses when they hear you're bringing a "gluten free" dish for a meal? I think that regular people don't understand that many things are naturally gluten-free. It might make them think twice about buying something. They think: gluten free? That probably doesn't taste as good as this non-gluten-free variety.

It's a matter of educating the population. But if we can't even educate Aunt Glenda, can you imagine how hard it's going to be to educate the rest of the world?

jerseyangel Proficient

At this point in the US, there isn't a true legal definition of "gluten-free". I much prefer when manufacturers clearly list any gluten in the ingredient list and if the product is processed on the same lines as those with gluten.

ravenwoodglass Mentor

That's why I will not move anyplace that doesn't have a Wegmans. They make shopping so easy for us. I have never had a CC reaction from any of their products and if I see the circle G I know the item is safe. I don't know why other companies don't do the same thing unless it is the liability issue or they just source their ingredients from places they are not sure of.

psawyer Proficient

There is a requirement in the USA and Canada (and likely most other places) that a label not be misleading.

To label something gluten-free implies that gluten-free is a factor which distinguishes this particular product from similar products. If the nature of the product is that it is inherently gluten-free, and all products of that type are gluten-free, then it is misleading (and illegal) to label it as gluten-free. You can have gluten-free pasta, gluten-free baked goods, gluten-free gravy, and so forth.

You can not, however, have gluten-free apples, gluten-free milk, gluten-free butter or gluten-free rice. Such products are allowed to say either:

"Xxxx is a gluten-free food." or

"This xxxx, like all xxxx, is gluten-free."

Where "xxxx" is the product type (not brand), for example "quinoa".


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



Celiac.com Sponsor (A8-M):



Juliebove Rising Star

I can see why people wouldn't want to put gluten-free on their labels. Cross contamination is highly likely. And many companies package their food on shared lines or in a facility that uses all sorts of ingredients. In such a case they would not want to use the gluten-free label even if the product is gluten-free in and of itself. Yes, I know some companies do this but I can see why they wouldn't want to.

tennisman Contributor

Thanks for all the replies.

Today I bought some Haribo sweets , even though I have had these sweets many times before ( but not for a few weeks ) I checked the ingredients and the Haribo still looked Gluten Free. But there was no " Gluten Free " on the packet. So I checked my Celiac book of what's Gluten Free and found out the Haribo was definitely Gluten Free :D Later I checked the Haribo website and it says Gluten Free.

Why can't they put this on the packet ? It's so annoying if they can put it's Gluten Free on there website why can't they put it on the packet ?

GFinDC Veteran

Thanks for all the replies.

Today I bought some Haribo sweets , even though I have had these sweets many times before ( but not for a few weeks ) I checked the ingredients and the Haribo still looked Gluten Free. But there was no " Gluten Free " on the packet. So I checked my Celiac book of what's Gluten Free and found out the Haribo was definitely Gluten Free :D Later I checked the Haribo website and it says Gluten Free.

Why can't they put this on the packet ? It's so annoying if they can put it's Gluten Free on there website why can't they put it on the packet ?

Good question. Maybe you could send them a an email and ask their reason. :)

tennisman Contributor

Good question. Maybe you could send them a an email and ask their reason. :)

I will do that :) If the company can put Gluten Free on there website than they can put Gluten Free on the packet . It's time for a change :)

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,857
    • Most Online (within 30 mins)
      7,748

    LowellFrancis
    Newest Member
    LowellFrancis
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Rogol72
      Some interesting articles regarding the use of Zinc Carnosine to help heal gastric ulcers, gastritis and intestinal permeability. I would consult a medical professional about it's use. https://www.nature.com/articles/ncpgasthep0778 https://www.rupahealth.com/post/clinical-applications-of-zinc-carnosine---evidence-review https://pmc.ncbi.nlm.nih.gov/articles/PMC7146259/ https://www.fallbrookmedicalcenter.com/zinc-l-carnosine-benefits-dosage-and-safety/
    • Jillian83
      He is. Which makes everything even more difficult. I’m not a believer in “staying for the kids” but I have nowhere to go and it’s not just me, it’s me plus my babies. We live in a beautiful place, lots of land in the country and me and the kids love the place we’ve called home for their entire lives. But Im seeing that he’ll never change, that my kids deserve a happy healthy Momma, and that staying in this as is will be the early death of me. Then I look at the scars covering my entire body…this disease and the chronic stress I’ve been enduring for years that tell me I’m no longer beautiful and no one will ever look at me with interest again. I try self care, try to give myself grace so I can just start loving myself enough to gain strength but the slightest sparkle in my eye and skip in my step attracts his wrath and it all comes crashing ten fold. Life is just absolutely railing me from every single direction leaving me wanting to wave that white flag bc I don’t feel like there’s much hope no matter what happens. 
    • trents
    • Jillian83
      Hi, I was recently diagnosed with Celiac and dermatitis herpetiformis after years of suffering without answers. I lost my mind. I lost my job. I lost so much time. I lost Me. Conventional doctors are opulent come near me and the one who did sat across the room, misdiagnosed me, pumped me full of steroids which collapsed my entire hip for 6 months. So without answers I began my holistic journey. Fast forward a couple of years and still struggling with a mysterious whole body itchy, crawling “skin hell”, perfect teeth now deteriorating, thick hair now thinning rapidly and no more than a day or 2 at most relief….An acquaintance opened up a functional medicine practice. Cash only, I found a way. Within a month tests clearly showing my off the charts gluten allergy/sensitivity as well as the depletion of vital nutrients due to leaky gut and intestinal damage. dermatitis herpetiformis was more than likely what I was experiencing with my skin. I was happy. I thought this is easy, eat healthy Whole Foods, follow the diet restrictions and I finally get to heal and feel confident and like myself again very soon! 😔 Supplements are very pricey but I got them and began my healing. Which leads to the other major issue: not working, stay at home Mom of young kids, entirely financially dependent on my man of 7 plus years. He’s never been supportive of anything I’ve ever done or been thru. He controls everything. I’m not given much money ever at a time and when he does leave money it’s only enough to possibly get gas. His excuse is that I’ll spend it on other things. So my “allowance” is inconsistent and has conditions. He withholds money from me as punishment for anything he wants. Since being diagnosed, he’s gained a new control tactic to use as punishment. He now is in control of when I get to eat. He asked for proof of my diagnosis and diet bc he said I made it up just to be able to eat expensive organic foods. Then after I sent him my file from my doctor he then said she wasn’t a real doctor. 😡. I go days upon days starving, sometimes breaking down and eating things I shouldn’t bc I’m so sick then I pay horribly while he gets annoyed and angry bc I’m not keeping up with all the duties I’m supposed to be doing. His abuse turns full on when I’m down and it’s in these desperate times when I need his support and care the most that I’m punished with silence, being starved, ignored, belittled. He will create more of a mess just bc I’m unable to get up and clean so that when I am better, I’m so overwhelmed with chores to catch up that the stress causes me to go right back into a flare from hell and the cycle repeats. I’m punished for being sick. I’m belittled for starving and asking for healthy clean water. I’m purposely left out of his life. He won’t even tell me he’s going to the grocery or to get dinner bc he doesn’t want me to ask him for anything. I have no one. I have nothing. Im not better. My supplements ran out and I desperately need Vitamin D3 and a methylated B complex at the very minimal just to function….he stares at me blankly…no, a slight smirk, no words. He’s happiest when im miserable and I am miserable.  this is so long and im condensing as much as I can but this situation is so complicated and disgusting. And it’s currently my life. The “IT” girl, the healthy, beautiful, perfect skin, perfect teeth, thick and curly locks for days, creative and talented IT girl….now I won’t even leave this house bc Im ashamed of what this has dont to my body, my skin. Im disgusted. The stress is keeping me from healing and I think he knows that and that’s why he continues to keep me in that state. He doesn’t want me confident or successful. He doesn’t want me healed and healthy bc then how would he put the blame of all his problems on me? This journey has been hell and I’ve been in Hell before. I’ve been killed by an ex, I’ve been raped, robbed, held hostage, abused beyond nightmares but the cruelty I’ve experienced from him bc of this disease is the coldest I’ve ever experienced. I’ve wanted to give up. Starving and in tears, desperate…I found a local food pantry in our small town so I reached out just saying I had Celiac and was on hard times. This woman is blessing me daily with prepared gluten free meals, donations, educational info, people who know this disease and how they manage life and the blessings just keep coming. But it’s overwhelming and I feel like I don’t deserve it at all. He just glared and I know he’s going to sabotage it somehow. I don’t even know what to do anymore. I’m so broken and just want peace and healing. 
    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
×
×
  • 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.