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

Snickers Bars In Australia


Olivegirl

Recommended Posts

Olivegirl Newbie

Hello all

I know that snickers bars in Australia are gluten free according to their label - but whenever I eat them, I get glutened type symptoms. Does this happen to anyone else? I'm assuming that perhaps they're processed on the same line as non-gluten-free goods ...


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



Celiac.com Sponsor (A8-M):



Saz Explorer

It is possible but usually this will be declared on the label, I've never noticed any warnings on the packet but maybe I'm not looking hard enough.

Not sure how new you are to been gluten-free but another possibility is the wheat glucose syrup. Although technically gluten free some very sensitive people find they react to it.

Also consider where you are buying them from. Coles and other supermarkets sell the ones made in Australia, but Crazy Clarkes etc sometimes sell imported ones. These don't always have same ingredients in them as the ones manufactured here.

I know you said it gives you gluten symptoms but maybe there is something else in the ingredients that don't agree with you?

It may not be something you are allergic to as such. I have no other allergies but I find that eating or drinking certain brands of some products just make feel sick.

Di2011 Enthusiast

I just drove up to the local servo (I'm near Canberra) and checked (((I am seriously treat/sweet/chocolate deprived!!!)))

Ingredients for both kinds of Snickers had "glucose syrup (sources can be wheat)" so unfortunately I am still treat deprived. :blink:

I can't tolerate much if any of the "derived from" products :(

pricklypear1971 Community Regular

I just drove up to the local servo (I'm near Canberra) and checked (((I am seriously treat/sweet/chocolate deprived!!!)))

Ingredients for both kinds of Snickers had "glucose syrup (sources can be wheat)" so unfortunately I am still treat deprived. :blink:

I can't tolerate much if any of the "derived from" products :(

What about nutella? I eat it off a spoon.

I also have great luck with peanut m&m's.

Saz Explorer

Not sure where you're from but Australian made m&ms aren't gluten-free. Some places sell the the American ones, I haven't checked for awhile but they used to be fine.

Di2011 Enthusiast

What about nutella? I eat it off a spoon.

I also have great luck with peanut m&m's.

oommgg.. i'm going to check this out tomorrow. Never been a "sweet tooth" but just about anything is sounding good right now.

Everything in small doses I must remember!!!

ElseB Contributor

My understanding was always that wheat based glucose is so highly refined that there isn't enough gluten left to be harmful.

I found a European Food Safety Authority article that is a bit less definitive (and is making me second guess my past consumption of wheat based glucose!):

For coeliac disease, assessment of the evidence produced including a new clinical study indicates that wheat-based glucose syrup is unlikely to cause an adverse reaction in individuals with coeliac disease provided that the (provisional) value of gluten considered by Codex Alimentarius for foods rendered gluten-free is not exceeded.

If you want to read the whole article, here's the link:

Open Original Shared Link


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



Celiac.com Sponsor (A8-M):



Di2011 Enthusiast

My understanding was always that wheat based glucose is so highly refined that there isn't enough gluten left to be harmful.

I found a European Food Safety Authority article that is a bit less definitive (and is making me second guess my past consumption of wheat based glucose!):

For coeliac disease, assessment of the evidence produced including a new clinical study indicates that wheat-based glucose syrup is unlikely to cause an adverse reaction in individuals with coeliac disease provided that the (provisional) value of gluten considered by Codex Alimentarius for foods rendered gluten-free is not exceeded.

If you want to read the whole article, here's the link:

Open Original Shared Link

I've been mostly gluten-free since June. Strictly gluten-free and low iodine for 2-3 months. I've gone basically to meat/fruit/veg/rice diet. Sometimes I add a rice noodle or gluten-free corn/rice pasta/rice thins.

If I have too much of the processed "gluten-free" and those that the authorities deem to be low enough to be (but not actually) "gluten-free" I tend to have serious trouble with DH.

It has only truly started to heal when I cut out the "gluten-free" (no gums, thickeners etc) in the past few weeks.

anabananakins Explorer

I just drove up to the local servo (I'm near Canberra) and checked (((I am seriously treat/sweet/chocolate deprived!!!)))

Ingredients for both kinds of Snickers had "glucose syrup (sources can be wheat)" so unfortunately I am still treat deprived. :blink:

I can't tolerate much if any of the "derived from" products :(

Cadbury's website has a good list, the plain dairy milk is fine. I like the rolls they sell (the shape that things like fruit pastells come in), with the little round tablet sized pieces of chocolate. You should be able to get that at the servo, even if they don't have the larger blocks.

(also, spending so much time on predominantly US-peopled websites that I'm used to North American english, it was fun see 'servo'! :) )

auzzi Newbie
If I have too much of the processed "gluten-free" and those that the authorities deem to be low enough to be (but not actually) "gluten-free" I tend to have serious trouble with DH.

I'm confused.

For it to be labelled "gluten free" in Australia, it must be 3ppm gluten or less [as of July 1 2011]. The labelling of "gluten free" is regulated and policed by Food Standards ANZ.

There is no "deemed low enough to be but not actually...": the science can't measure lower than than 3ppm, so no-one can say for absolute certain the "gluten-

free" is really "gluten-free".

Naturally "gluten-free" products are contaminated all the time .. meats, vegetables, fruits ... depends on how they are handled. But, Food Standards ANZ tests everything, even those ..

As for 20ppm, 100ppm, 200ppm in Australia: imported gluten-free items have to be "gluten free" according to our regulations of 3ppm or less..

..

Di2011 Enthusiast

I'm confused.

For it to be labelled "gluten free" in Australia, it must be 3ppm gluten or less [as of July 1 2011]. The labelling of "gluten free" is regulated and policed by Food Standards ANZ.

There is no "deemed low enough to be but not actually...": the science can't measure lower than than 3ppm, so no-one can say for absolute certain the "gluten-

free" is really "gluten-free".

Naturally "gluten-free" products are contaminated all the time .. meats, vegetables, fruits ... depends on how they are handled. But, Food Standards ANZ tests everything, even those ..

As for 20ppm, 100ppm, 200ppm in Australia: imported gluten-free items have to be "gluten free" according to our regulations of 3ppm or less..

..

Sorry, hadn't intended to confuse. I had worked in a bakery for 9months until May/June and my system was so overloaded. DH has been a head-to-ankle nightmare. I still wear clothes from neck to ankle and itch pretty much all day. Regardless of whether it is gluten, salts (iodine) etc in the processed goods the bulk are on my avoid list. I didn't have any significant progress until I took out these products.

I have had the same problems with bathroom products. I've had some absolute nightmares with some of the most basic products (naturals, organics, anything) that have gums and other so called gluten-free wheat chemicals with lots of pseudonyms.

I don't have any issues with the authority/regulations/testing etc. I just know from months of experimenting that it doesn't work for me.

Olivegirl Newbie

Thanks everyone for your responses! I don't normally react to wheat glucose syryp, nor do I have other allergies - but I must admit I haven't tried a snickers in over a year - so maybe I should ty again and see what happens? (and make sure it's one that's manufactured here, not overseas). I occassionally have the same problem with the snack size cadubury's plain chocolate - but not always. So it could be something to do with chocolate per se perhaps.

beebs Enthusiast

I eat snickers all the time and have never had a problem, I'm not super sensitive or anything.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,963
    • Most Online (within 30 mins)
      7,748

    AlissaW
    Newest Member
    AlissaW
    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

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • 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.