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

Cadbury Cream Eggs- Now With Wheat :(


SuperGina

Recommended Posts

cruelshoes Enthusiast

Thanks for the heads up. I posted this info on a couple of other celiac boards that I go to. A lot of people will be totally bummed. Makes me glad I don't like these things. ;)


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



Celiac.com Sponsor (A8-M):



alamaz Collaborator

My day is officially ruined (although, I wouldn't have read ingredients and it could have been a lot worse!). Figures the year I'm pregnant and craving just about anything bad for me Cadbury eggs have to become un-gluten free!

Shame on Hershey's!

I'd be interested to see an ingredient listing from pre labeling laws to see if they added the glucose recently or just started labeling it recently.....

melrobsings Contributor

I wrote to the and complained. I'll let you know if I hear anything.

cruelshoes Enthusiast

I do not like Cadbury Creme eggs, but it appears that Glucose syrup, even if derived from wheat, is a gluten free ingredient. I think it will be another decision we all have to make like the one on McDonald's fries, but below is information on this ingredient. I suspect that there has been no change to the ingredients for the creme eggs, only that the labeling laws now require that the source of the glucose syrup be disclosed.

Irish Daveyboy already posted this one, but here it is again:

GLUCOSE, GLUCOSE SYRUP AND CARAMEL COLOUR

It is important for those following a gluten-free diet to incorporate the latest valid scientific information into their diets. Under current Australian food law, glucose, glucose syrup and caramel colour are "gluten-free", even if derived from wheat, as the wheat is so highly processed, there is no gluten detected.

Glucose, glucose syrup, caramel and similar ingredients have no detectable gluten, even if derived from wheat. New food labelling laws require food labels to list all ingredients derived from wheat, rye, barley and oats. This does not mean that all ingredients derived from these sources actually contain gluten. So, it is a legal requirement that the source be declared, but remember that ingredients derived from wheat that are gluten free are: dextrose, glucose and caramel colour (additive 150). "

"Open Original Shared Link" Shelley Case, author.

page: 53- "Glucose syrups are highly processed and purified in order to separate and remove the protein portion from the starch mixture. .... Although glucose syrup can be made from wheat, the processing renders it gluten free. This has been verified by scientists and research centers in Europe, Australia and other countries using the highly sensitive R5 ELISA tests."

Lisa Mentor

So.....dextrose, glucose and caramel color are ALWAYS gluten free even if listed (wheat)?

I have seen these ingredients often and have never been concerned, but rarely have I seen the source listed as (wheat).

blueeyedmanda Community Regular
So.....dextrose, glucose and caramel color are ALWAYS gluten free even if listed (wheat)?

I have seen these ingredients often and have never been concerned, but rarely have I seen the source listed as (wheat).

This was the first I have ever seen it listed this way either....but seeing as it says wheat I am going to stay away from it. As long as they keep the Cadbury Mini Eggs gluten free.....once they use gluten in those We will have LOTS of problems.

  • 2 weeks later...
gfp Enthusiast

Not long ago 200ppm (the lowest detection limit for cheap testing) was considered safe.

Now cheap testing goes to 20 or 5 ppm ...

For many years current scientific research could make no definitive statement that smoking causes cancer.

I would say when people make their descision that current scientific research is not the last word...

I am certainly unaware of any long term studies on this (and there hasn't even been time) ... but I would be more worried what future scientific research will say when long term studies have been made.


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



Celiac.com Sponsor (A8-M):



Ms. Celiac Apprentice

Are Cadbury eggs that are sold in the UK still gluten free?

Worriedtodeath Enthusiast
Not long ago 200ppm (the lowest detection limit for cheap testing) was considered safe.

Now cheap testing goes to 20 or 5 ppm ...

For many years current scientific research could make no definitive statement that smoking causes cancer.

I would say when people make their descision that current scientific research is not the last word...

I am certainly unaware of any long term studies on this (and there hasn't even been time) ... but I would be more worried what future scientific research will say when long term studies have been made.

HearHear!!!! Scientific research is also usually backed by the very people trying to make a buck by having said research turn out for their best bottom dollar. Current medical scientific research tells my whole gang to eat wheat to our heart's content because we have no medical scientific reason to avoid it despite severe sickness and undeniable positive results from a gluten-free diet. The only research that might change that has not been published yet or examined by other scientist yet so thus it is unknown.

While it is nice to know that today's research claims it is safe, in 50 years will they say the same as technology becomes better???

And if you are allergic to wheat, would you still react?? If so then it still has enough wheat to cause someone a problem. And thus still trip autoimmune reactions.

Stacie

gfp Enthusiast
HearHear!!!! Scientific research is also usually backed by the very people trying to make a buck by having said research turn out for their best bottom dollar. Current medical scientific research tells my whole gang to eat wheat to our heart's content because we have no medical scientific reason to avoid it despite severe sickness and undeniable positive results from a gluten-free diet. The only research that might change that has not been published yet or examined by other scientist yet so thus it is unknown.

While it is nice to know that today's research claims it is safe, in 50 years will they say the same as technology becomes better???

And if you are allergic to wheat, would you still react?? If so then it still has enough wheat to cause someone a problem. And thus still trip autoimmune reactions.

Stacie

This is the bottom line ....

The 200ppm limit was set by the food industry, not based on scientific study.

The food industry itself then paid for the studies saying celiacs were no worse off on 200ppm than a 'normal' gluten-free diet.

This in itself is fundamentally flawed... it took 50 yrs to 'prove' smoking causes cancer ... and this was in the face of a lot of evidence because its so easy to fix a clinical trial.

You can start by pre-screening candidates ... the ones you worry about you throw out. So in the case of a gluten-free test you just make sure those on a gluten-free diet have no idea about hidden gluten or cross contamination....

Its hardly difficult, most of us comiong here had no idea until we found this board!

Then you say '200ppm limit' .. again fine this doesn't mean the test sample are eating 200ppm, just they are eating something with 'some gluten' which of course can be controlled specifically. 200ppm was not the limit for testing, it was the limit for testing my ELISA tests, GC-MS could for the last 20 yrs detect <1ppm. Its just more expensive but hey, if your doing a study you do one set of tests to determine its VERY LOW and a seperate set of qualitative tests to say 'its present'

The tobacco industry used this type of leveraged testing successfully for 50 yrs.

Really, you have to wonder why their testing is even considered valid?

wildchild-nan Newbie

I know it is in the caramel ones, I was so bummed. It was one of the things I look foward to this time of the year.

angielackner Contributor

i am not celiac, but i at least have a gluten intolerance, but i honestly think it is either a gluten ALLERGY or wheat allergy...sigh

anyways...i first bought a batch of the minis and ate them with no problem, then got the full sized ones (3 of them mind you) a few days later and sucked them all down that evening (nothing new there for me...i do it every year)...but i got an itchy throat after eating the full sized ones, like i do with a glutening...i never read the labels as i blindly trusted they were still gluten free...i mean come one, who messes with perfection on a recipe?!?!?! crazy!

so yeah, i must have reacted to the wheat in them.

ughhhhh!

angie

HeartofGlass224 Rookie

Figures...this is the one candy that I wait all year to be able to get at Easter! :( Thanks for the info!

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. - DebD5 commented on Scott Adams's article in Spring 2026 Issue
      1

      The Dark Side of Gluten-Free: Counterfeit Labels and Global Food Safety Failures

    2. - Jmartes71 replied to Jmartes71's topic in Doctors
      6

      Second chance

    3. - trents replied to EssexMum's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      2

      Concerning GP advice

    4. - knitty kitty replied to HectorConvector's topic in Related Issues & Disorders
      327

      Terrible Neurological Symptoms

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

    • Total Members
      133,643
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • Jmartes71
      Thats the thing, diagnosed in 1994 before foods eliminated celiac by biopsy colonoscopy at Kaiser in Santa Clara  now condo's but it has to be somewhere in medical land.1999 got married, moved, changed doctor's was with former for 25 years told him I waz celiac and that.Fast forward to last year.i googled celiac specialist and what popped up was a former well known heard of hospital. I thought I would get answers to be put through unnecessary colonoscopy KNOWING im glutenfree and she wasn't listening to me for help rather than screening me for celiac! Im already diagnosed seeking medical help.I did all the appointments ask from her and when I wanted my records se t to my pcp, thats when the with holding my records when I repeatedly messaged, it was down played the seriousness and I was labeled unruly when I asked why am I going through all this when its the celiac name that IS what my issue and All my ailments surrounding it related. I am dea6eoth the autoimmune part though my blood work is supposedly fabulous. Im sibo positive,HLA-DQ2 positive, dealing with skin, eye and now ms.I was employed as a bus driver making good money, I loved it for the few years my body let me do until I was yet again fired.i went to seek medical help because my body isn't well just to be made a disability chaser. Im exhausted,glutenfree, no lawyer will help and disability is in limbo thanks to the lax on my health from the fabulous none celiac Google bay area dr snd team. Its not right.
    • trents
      Welcome to the celiac.com community @EssexMum! First, let me correct some misinformation you have been given. Except in the case of what is known as "refractory" celiac disease, which is very rare, it is not true that the "fingers" will not grow back once a consistently gluten free diet is adopted. Celiac disease is an autoimmune condition whereby the ingestion of gluten triggers an inflammatory process that damages the millions of tiny finger-like projections that make up the lining of the small bowel. We call this the "villous lining". Over time, continued ingestion of gluten on a regular basis results in the wearing down of these fingers which greatly reduces the surface area of this very important membrane. It is where essentially all the nutrition from what we eat is absorbed. So, losing this surface area results in inefficiency in nutrient absorption and often to medical problems related to nutrient deficiencies. Again, if a gluten-free diet is consistently observed, the villous lining of the small bowel should rebound. "We was informed that her body absorbs the gluten rather then rejecting it and that is why she doesn't react to the gluten straight away, it will be a build up and then the pains start. " That sounds like unscientific BS to me. But it does sound like your stepdaughter may have a type of celiac disease we know as "silent" celiac disease, meaning, she is asymptomatic or at least the symptoms are not intense enough to usually notice. She is not completely asymptomatic, however, because you stated was experiencing tummy aches off and on. Cristiana gives some good suggestions about ordering "safe" food for your stepdaughter from restaurant menus in Europe. You must realize that as the step parent who only has her part of the time you have no real control over how cooperative her other set of parents are with regard to your stepdaughter's needs to eat gluten free. It sounds like they don't really understand the seriousness of the matter. This is very common in family settings where other members are ignorant about celiac disease and the damage it can do to body systems. So, they don't take it seriously. The best you can do is make suggestions. Perhaps print out some info about celiac disease from the Internet to send them. Being inconsistent with the gluten free diet keeps the inflammation smoldering and delays or inhibits healing of the villous lining. 
    • Scott Adams
      Here are some articles on cross-reactivity and celiac disease:      
    • knitty kitty
      @HectorConvector, Here are some articles about "dry Beriberi" and neuropathy.  I hope you've been able to acquire thiamine hydrochloride or Benfotiamine.  I'm concerned.   Dry Beriberi Due to Thiamine Deficiency Associated with Peripheral Neuropathy and Wernicke's Encephalopathy Mimicking Guillain-Barré syndrome: A Case Report and Review of the Literature https://pubmed.ncbi.nlm.nih.gov/30862772/ Dry Beriberi Manifesting as Acute Inflammatory Demyelinating Polyneuropathy in a Patient With Decompensated Alcohol-Induced Cirrhosis https://pmc.ncbi.nlm.nih.gov/articles/PMC7707918/ A Rare Case of Thiamine Deficiency Leading to Dry Beriberi, Peripheral Neuropathy, and Torsades De Pointes https://pmc.ncbi.nlm.nih.gov/articles/PMC10723625/
    • cristiana
      Good evening @EssexMum You are quite right to be concerned about this situation.  Once diagnosed as coeliac, always a coeliac, and the way to heal  is through adopting and sticking to a strict gluten diet. That said... I have travelled twice to France since my diagnosis, firstly in May 2013 and again in August 2019.   My spoken French isn't bad, and whilst there I tried my best to explain my needs to chefs and catering staff, and I read labels very carefully when shopping in supermarkets, but both times I came away with worsening gastric symptoms and pain. Interestingly,  after the second holiday, my annual coeliac review took place the following month and although I'd been very careful to avoid gluten all year, thanks to that August holiday my coeliac antibodies were elevated,  Clearly I hadn't been imagining these symptoms and they must have been caused by gluten sneaking in somehow. When I spoke to my gastroenterologist on my return, who is an excellent doctor, he told me with a smile that this was a very common experience in France among his patients, and not to worry too much about it! In fact, before we went away in May 2013, which was just after I had been formally diagnosed, he told me not to even bother trying to adopt a gluten free diet until I returned, knowing what France was like, but I was feeling so awful at that time I ignored his advice and at least tried to make a start with it. (I ought to say - both these visits were some time ago, so perhaps things are a lot better there now.) So what to do?  I would say at least try to explain to catering staff the situation - they should be able to rustle up a plate of cheese, boiled eggs, tuna, salad and fruit, and if things like crackers and gluten-free pot noodle or oats can be packed in the UK, those can be produced at mealtimes.    Of course, most larger supermarkets in France do now cater for coeliacs, but when I was last there the the choice wasn't as wide a range as we have in the UK but I think that is partly because the French like to cook from scratch, whereas our gluten-free aisles have quite a lot of dried or pre-baked goods in them/convenience foods, because I think we as a nation tend to use them more. I would be worth doing a bit of research on the internet before the trip, - the words you want are 'sans gluten'.  I've just googled 'sans gluten Disney Paris" and this came up.  I do hope at least some of this is of help. https://www.tripadvisor.co.uk/Restaurants-g2079053-zfz10992-Disneyland_Paris_Ile_de_France.html  Whatever befalls in France, at least your stepdaughter can resume her usual diet on her return. On a related tack, would you be happy to post any positive findings/tips upon her return - it might be of use to others travelling to Disneyland Paris with children in future? 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.