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Canadians?


EMSPrincess

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EMSPrincess Newbie

Hi... I'm just wondering if I'm the only Canadian on here. I've just recently been diagnosed and found this forum and liked what I saw but it seems to be only americans which might be a little difficult for getting specific help, and food, and shopping ideas. I love the help I've already gotten from some of you though, you guys are very helpful!

So just looking for Canadians for more help with shopping, stores, support groups etc...


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  • Replies 223
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Lisa Mentor

Trust me!!! There are lots of Canadians here, eh. :rolleyes:

They'll be with you soon.

Rusla Enthusiast

Hi Lisa,

You are definitely not the only Canadian here. We have it covered from West coast to the East coast and in between. Where are you ?

There is lots of good info here, although I must admit I am jealous of the Americans for all the food choices they can get.

Felidae Enthusiast

There may be fewer of us, but we are here to help.

Canadian Karen Community Regular

Hi EMSPrincess!

Welcome to the forum! I am in Ontario, just outside of Toronto.....

Where are you?

Karen

psawyer Proficient

Yeah, there a bunch of us. I'm not far from Toronto. Welcome!

lorka150 Collaborator

i am canadian, too!


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Guest Viola

Hello, I'm also Canadian ... Western Canada near Nelson B.C. Anything we can help with we'll be glad to give you answers to Canadian products and Stores. Previding we have them of course, but with some of us in all the provinces, we should come up with something. :D

KarenCM Rookie

I am Canadian too! Have you joined the Canadian Celiac Association yet? They can be helpful as well.

Karen

EMSPrincess Newbie

Thanks everyone.. I'm from Peterborough, On.. I looked into the Canadian Celiac Ass., but the chapter in Peterborough doesn't seem very active...

Is there somewhere on here for Canadians??

Anyone from around me any food/restaurant/etc. suggestions.. Thanks again everyone... I'm having a really tough time with this.

Lisa Mentor
Hi Lisa,

You are definitely not the only Canadian here. We have it covered from West coast to the East coast and in between. Where are you ?

There is lots of good info here, although I must admit I am jealous of the Americans for all the food choices they can get.

I live in North Carolina, USA. But I know how sassy you Canadians can be. Especially when it gets dark early and mints are the only source of entertainment....har,har,har. :ph34r:

Canadian Karen Community Regular
I live in North Carolina, USA. But I know how sassy you Canadians can be. Especially when it gets dark early and mints are the only source of entertainment....har,har,har. :ph34r:

:lol::lol::lol:

Altoids rock! (except Tuesdays at 9 pm)

Karen

Lisa Mentor

Moon Pies and Dr. Pepper, don't do alot for me here in the land down under. I'm still trying to find out what does :blink::blink: Altoid, wasn't that a figure in greek mythogoly? :rolleyes:

Welcome Canadians, and hugs back to Karen

Carriefaith Enthusiast

I'm a Canadian too! I've posted some information in the Gluten-Free International Room (Outside USA) forum Open Original Shared Link

If you need any information about gluten free products in Canada, please feel free to ask!

lorka150 Collaborator

are you a student, EMSPrincess?

are all of you going to the conference in May?

skoki-mom Explorer

Hello, count me in :) I am in Calgary.

num1habsfan Rising Star

I'm from Saskatchewan...come on lets find someone from every province :lol:

~lisa~

Ursa Major Collaborator

Well, I'm not Canadian, but I'm in Canada, about an hours drive north of Toronto.

Guest chickadee
Hi... I'm just wondering if I'm the only Canadian on here. I've just recently been diagnosed and found this forum and liked what I saw but it seems to be only americans which might be a little difficult for getting specific help, and food, and shopping ideas. I love the help I've already gotten from some of you though, you guys are very helpful!

So just looking for Canadians for more help with shopping, stores, support groups etc...

Hi :lol: I'm also from Canada. PEI to be more exact. Welcome to the family. This sight is excellent and I would not survive without it. Just remember that this board is predominantly USA, and sometimes the information given will not apply to us here in Canada. I found out the hard way :blink:

So stay on board and we look forward to chatting.

Carriefaith Enthusiast
are all of you going to the conference in May?
I would love to go, but if I get a job within the next month or so, I probably won't be able to attend unless I get a job in southern Ontario.
Rusla Enthusiast

I am also in Calgary.

No wonder I am lacking excitement, I am all out of mints.

silly-yak-mum Apprentice

Welcome EMS! Another Cdn here. I'm just outside Toronto. If you haven't done so yet, check out Kawartha Bakery - it's close to Peterborough and worth the short drive! There's a bakery that makes fresh bread, cinnamon buns, meat pies, etc. (I buy them at a health food store in Whitby shipped from Lakefied.) ALSO - they have a small restaurant attached to the bakery with many gluten-free options. My son loved the grilled cheese and fries. I don't even remember which dessert he settled on. Enjoy!

Open Original Shared Link

sasha1234 Newbie

I'm from Canada too, Edmonton, and also new to all this. I'm in the process of being diagnosed, just had my biospies on thursday. I had been off of gluten for 4 years prior to the 6 weeks leading up to the test so I've got the hang of eating gluten free but I'm sure I'll have loads of other questions.

  • 3 weeks later...
elye Community Regular

I'm from Ottawa, and yes, I think I'm going to go to the conference. Lots of contacts and info to be picked up there, for sure. Anyone else going?

Canadian Karen Community Regular

I going to go too!

Karen

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    • captaincrab55
      Imemsm, Most of us have experienced discontinued, not currently available or products that suddenly become seasonal.   My biggest fear about relocating from Maryland to Florida 5 years ago, was being able to find gluten-free foods that fit my restricted diet.  I soon found out that the Win Dixie and Publix supper markets actually has 99% of their gluten-free foods tagged, next to the price.  The gluten-free tags opened up a  lot of foods that aren't actually marked gluten-free by the manufacture.  Now I only need to check for my other dietary restrictions.  Where my son lives in New Hartford, New York there's a Hannaford Supermarket that also has a gluten-free tag next to the price tag.  Hopefully you can locate a Supermarket within a reasonable travel distance that you can learn what foods to check out at a Supermarket close to you.  I have dermatitis herpetiformis too and I'm very sensitive to gluten and the three stores I named were very gluten-free friendly.  Good Luck 
    • rei.b
      Okay well the info about TTG-A actually makes a lot of sense and I wish the PA had explained that to me. But yes, I would assume I would have intestinal damage from eating a lot of gluten for 32 years while having all these symptoms. As far as avoiding gluten foods - I was definitely not doing that. Bread, pasta, quesadillas (with flour tortillas) and crackers are my 4 favorite foods and I ate at least one of those things multiple times a day e.g. breakfast with eggs and toast, a cheese quesadilla for lunch, and pasta for dinner, and crackers and cheese as a before bed snack. I'm not even kidding.  I'm not really big on sugar, so I don't really do sweets. I don't have any of those conditions.  I am not sure if I have the genes or not. When the geneticist did my genetic testing for EDS this year, I didn't think to ask for him to request the celiac genes so they didn't test for them, unfortunately.  I guess another expectation I had is  that if gluten was the issue, the gluten-free diet would make me feel better, and I'm 3 months in and that hasn't been the case. I am being very careful and reading every label because I didn't want to screw this up and have to do gluten-free for longer than necessary if I end up not having celiac. I'm literally checking everything, even tea and anything else prepacked like caramel dip. Honestly its making me anxious 😅
    • knitty kitty
      So you're saying that you think you should have severe intestinal damage since you've had the symptoms so long?   DGP IgG antibodies are produced in response to a partial gluten molecule.  This is different than what tissue transglutaminase antibodies are  produced in response to.   TTg IgA antibodies are produced in the intestines in response to gluten.  The tTg IgA antibodies attack our own cells because a structural component in our cell membranes resembles a part of gluten.  There's a correlation between the level of intestinal damage with the level of tTg antibodies produced.  You are not producing a high number of tTg IgA antibodies, so your level of tissue damage in your intestines is not very bad.  Be thankful.   There may be reasons why you are not producing a high quantity of tTg IgA antibodies.  Consuming ten grams or more of gluten a day for two weeks to two months before blood tests are done is required to get sufficient antibody production and damage to the intestines.  Some undiagnosed people tend to subconsciously avoid lots of gluten.  Cookies and cakes do not contain as much gluten as artisan breads and thick chewy pizza crust.  Anemia, diabetes and thiamine deficiency can affect IgA antibody production as well.   Do you carry genes for Celiac?  They frequently go along with EDS.
    • rei.b
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