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

Are Smarties gluten-free?


TriticusToxicum

Recommended Posts

TriticusToxicum Explorer

CAn I have some? Please say yes! :huh:


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



Celiac.com Sponsor (A8-M):



CarlaB Enthusiast

I don't know .... but some smart pills would definately be good for you!!! :lol:

TriticusToxicum Explorer

Who let the rif-raf in? :huh:

This is a topic full of serious scientificness :P

(i thought they were smart pills- no? :huh: )

CarlaB Enthusiast

Yeah, they are smart pills, so they might be worth the risk in your case. ;)

jerseyangel Proficient

Richard,

Smarties, in the US are gluten-free. (I believe that in Canada, they are not)

TriticusToxicum Explorer
Richard,

Smarties, in the US are gluten-free. (I believe that in Canada, they are not)

I'll be sure to eat them on this side of the border! :P

Thanks - you made my day! :)

CarlaB Enthusiast

I knew Patti'd be able to answer!!! She knows all the candy answers!!


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



Celiac.com Sponsor (A8-M):



TriticusToxicum Explorer
Yeah, they are smart pills, so they might be worth the risk in your case. ;)

That'll make me 5pts smarter than you, but who's counting? :P

Canadian Karen Community Regular

Smarties in Canada definitely have gluten in them...... :angry:

CarlaB Enthusiast
That'll make me 5pts smarter than you, but who's counting? :P

Wow, since I can't have sugar, you will definately be smarter than me by the end of the day!!!

Smarties in Canada definitely have gluten in them...... :angry:

Yeah, but Altoids don't, who needs Smarties anyway?! :P

TriticusToxicum Explorer

Ok Karen got me wondering. On the wrapper it says "made in Canada" :(

BUT... Open Original Shared Link :)

so I'm going for it!

nikki-uk Enthusiast
Richard,

Smarties, in the US are gluten-free. (I believe that in Canada, they are not)

Smarties are NOT gluten-free in the UK either alas...hubby misses them :( ...

blueeyedmanda Community Regular

TriticusToxicum- I have just got to say, love the picture. The Shining is a great movie!

2kids4me Contributor

M & M's are gluten free - in Canada . I did not know smArties in the US are Gluten free!!

My son will want to make border trip!!

hez Enthusiast

My understanding (not being in Canada) is that the smarties in the US are a different candy. The smarties in Canada are similar to m&ms. The US smarties are a sugary treat, no chocolate.

Hez

CarlaB Enthusiast

So, what's your IQ now, Richard?

debmidge Rising Star

As an aside, I sort of remember that they might have lactose in them...? check that out if you are lactose intolerant too.

Guest nini

my Canadian sister in law tells me that Smarties in Canada are a chocolate candy like m&m's and that American Smarties are sugary tablets... I'm addicted to those sugary things. (I think I ate 6 pks and 5 tootsie rolls today while waiting to pick up my daughter from school ;)

2Boys4Me Enthusiast

Canadian Smarties are chocolate sort of, but not quite like M&Ms.

Canadian Rockets=U.S. Smarties.

Rockets are gluten-free.

shai76 Explorer

US Smarties are free of all common allergens...that is what makes them so awesome! BUt they still have corn in them. :(

They used to be corn free.

skoki-mom Explorer
Canadian Smarties are chocolate sort of, but not quite like M&Ms.

Canadian Rockets=U.S. Smarties.

Rockets are gluten-free.

Yeah, Smarties are way better than M&Ms, and I miss them. I always ate the red ones last :(

Ursa Major Collaborator

I had no idea that smarties can be anything other than chocolate candies, how confusing! :huh:

2Boys4Me Enthusiast

Lori- don't get me started. My husband and I always have arguments about this. I think that M&Ms are the superior candy and he thinks smarties. Then he starts the debate about how M&Ms are acceptable only if they are peanut M&Ms. I personally think the original M&Ms are superior and now I want some. :ph34r:

Ruth52 Newbie

Australian Smarties are like M&M's. Chocolate in the middle and a think layer or colored candy on the outside.

Ruth.

georgie Enthusiast

NO CHOCOLATE ???!!!

. The US smarties are a sugary treat, no chocolate.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,635
    • Most Online (within 30 mins)
      7,748

    dysmathers
    Newest Member
    dysmathers
    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

    • deanna1ynne
      Dd10 was tested for celiac four years ago bc two siblings were dx’d (positive labs and biopsies). Her results at the time were positive ema  and ttg (7x the UL), but a negative biopsy. We checked again three months later and her ttg was still positive (4x the UL), but ema and biopsy were negative. Doc said it was “potential celiac” and to keep eating gluten, but we were concerned about harming her growth and development while young and had her go gluten-free because we felt the labs and ema in particular were very suggestive of early celiac, despite the negative biopsies. She also had stomach aches and lethargy when eating it. We just felt it’d be better to be safe than sorry. Now, four years later, she doesn’t want to be gluten-free if she doesn’t “have to be,” so underwent a 12 week gluten challenge. She had labs done before starting and all looked great (celiac panel all negative, as expected.) Surprisingly, she experienced no noticeable symptoms when she began eating gluten again, which we felt was a positive sign. However, 12 weeks in, her labs are positive again (ttg 4x the UL and ema positive again as well). Doc says that since she feels fine and her previous two biopsies showed nothing, she can just keep eating gluten and we could maybe biopsy again in two years. I was looking up the ema test and the probability of having not just one but two false positives, and it seems ridiculously low.  Any advice? Would you biopsy again? She’s old enough at this point that I really feel I need her buy-in to keep her gluten-free, and she feels that if the doc says it’s fine, then that’s the final word — which makes me inclined to biopsy again and hope that it actually shows damage this time (not because I want her to have celiac like her sisters, but because I kind of think she already does have it, and seeing the damage now would save her more severe damage in the long run that would come from just continuing to eat gluten for a few more years before testing again.)  Our doc is great - we really like him. But we are very confused and want to protect her. One of her older sibs stopped growing and has lots of teeth problems and all that jazz from not catching the celiac disease sooner, and we don’t want to get to that point with the younger sis. fwiw- she doesn’t mind the biopsy at all. It’s at a children’s hospital and she thinks it’s kind of fun. So it’s not like that would stress her out or anything.
    • Inkie
      Thanks for the replies. I already use a gluten-free brand of buckwheat flakes I occasionally get itchy bumps. I'm still reviewing all my food products. I occasionally eat prepackaged gluten-free crackers and cookies, so I'll stop using those. I use buckwheat flakes and Doves Farm flour as a base for baking. Would you recommend eliminating those as well? It's a constant search.
    • Wheatwacked
      Gluten free food is not fortified with vitamins and minerals as regular food is.  Vitamin deficiencies are common especially in recently diagnosed persons,  Get a 25(OH)Vitamin D blood test. And work on raising it.  The safe upper blood level is around 200 nmol/L.    "Low serum levels of 25(OH)D have been associated with increased risk of autoimmune disease onset and/or high disease activity. The role of vitamin D in autoimmune diseases   🏋️‍♂️Good job!   I find the commercial milk will give me mild stomach burn at night, while pasture/grassfed only milk does not bother me at all.  While you are healing, listen to your body.  If it hurts to eat something, eat something else.  You may be able to eat it later, or maybe it is just not good for you.  Lower your Omega 6 to 3 ratio of what you eat.  Most omega 6 fatty acids are inflammation causing.    The standard american diet omega 6:3 ratio is estimated at upward of 14:1.  Thats why fish oil works
    • Inkie
      I  notice a reaction to tea bags, possibly due to gluten or other substances. Is this recognizable?
    • trents
      The blood tests you had done are not the main ones. The two main ones are the "Total IGA" (to check for IGA deficiency) and the "TTG-IGA". Current guidelines for the "gluten challenge" when people have been gluten free for a significant time period are the daily consumption of at least10g of gluten (about the amount in 4-6 slices of wheat bread) for at least two weeks leading up to the day of the blood draw. That should give you some perspective.
×
×
  • 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.