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New Celiac Pocket Dictionary

fisharefriendsnotfood

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fisharefriendsnotfood Apprentice
fisharefriendsnotfood
Posted

The New Celiac Pocket Dictionary just arrived in the mail today from the Canadian Celiac Assosiation. I'm very excited because it has EVERYTHING in it, what it is, and whether or not it's allowed. It's small so we can just carry it around! If anyone has questions about what's allowed, post here and I'll post the answer. I have my handy-dandy pocket dictionary here lol.

-Jackie

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Lisa Mentor
Lisa
Posted

Cool:

Anyone have a US version?

Lisa B

Eliza13 Contributor
Eliza13
Posted

Heehee...

Just received mine too!!

AmandaD Community Regular
AmandaD
Posted

Could you tell me where you got this, so I can order one as well? thanx!

The New Celiac Pocket Dictionary just arrived in the mail today from the Canadian Celiac Assosiation. I'm very excited because it has EVERYTHING in it, what it is, and whether or not it's allowed. It's small so we can just carry it around! If anyone has questions about what's allowed, post here and I'll post the answer. I have my handy-dandy pocket dictionary here lol.

-Jackie

<{POST_SNAPBACK}>

fisharefriendsnotfood Apprentice
fisharefriendsnotfood
Posted
  • Author
Could you tell me where you got this, so I can order one as well?  thanx!

<{POST_SNAPBACK}>

I got mine through the Canadian Celiac Assosiation, of which I am a member.

KarenCM Rookie
KarenCM
Posted

I am so excited I can't wait to get mine in the mail. It is so nice that they are mailing a new one to everyone of the members.

Here is a link to the page if any non members were wondering about it. It is only $7.95 for a non member to buy.

Open Original Shared Link

Open Original Shared Link

Karen

skoki-mom Explorer
skoki-mom
Posted

Well, now I definitely have to get over there and get my membership!! I've been so friggin busy, I just keep forgetting!

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psawyer Proficient
psawyer
Posted

I obtained a copy of the previous (1992) edition within a month of being diagnosed. I bought a copy at a specialty store that sells, among other things, gluten free food. I too received a complimentary copy of the new edition in today's mail. I used it very frequently at first, but over time I got to know most of the common things, so I don't need it as often. I still use if, though, and if you are new to the diet it is a must have.

You don't have to be a member to buy a copy, but if you are not in Canada you should know that some of the things are declared gluten-free based on Canadian labelling rules, which could differ in other contries. For example, on a Canadian food label "starch" is corn starch unless another source is explicitly stated. I know this is NOT true in the US.

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  • Posts

    • Mari
      New Celiac Mama in My 30s

      By Mari · Posted

      There is much helpful 'truth' posted on this forum. Truths about Celiac Disease are based on scientific research and people's experience. Celiac disease is inherited. There are 2 main Celiac 'genes' but they are variations of one gene called HLa - DQ What is inherited when a person inherits one or both of the DQ2 or the DQ8 is a predisposition to develop celiac disease after exposure to a environmental trigger. These 2 versions of the DQ gene are useful in diagnosing  celiac disease but there are about 25 other genes that are known to influence celiac disease so this food intolerance is a multigenic autoimmune disease. So with so many genes involved and each person inheriting a different array of these other genes one person's symptoms may be different than another's symptoms.  so many of these other genes.  I don't think that much research on these other genes as yet. So first I wrote something that seem to tie together celiac disease and migraines.  Then you posted that you had migraines and since you went gluten free they only come back when you are glutened. Then Scott showed an article that reported no connection between migraines and celiac disease, Then Trents wrote that it was possible that celiacs had more migraines  and some believed there was a causal effect. You are each telling the truth as you know it or experienced it.   
    • tiffanygosci
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      Thank you all for sharing your experiences! And I am very thankful for that Thanksgiving article, Scott! I will look into it more as I plan my little dinner to bring with on the Holiday I'm also glad a lot of research has been done for Celiac. There's still a lot to learn and discover. And everyone has different symptoms. For me, I get a bad headache right away after eating gluten. Reoccurring migraines and visual disturbances were actually what got my PCP to order a Celiac Panel. I'm glad he did! I feel like when the inflammation hits my body it targets my head, gut, and lower back. I'm still figuring things out but that's what I've noticed after eating gluten! I have been eating gluten-free for almost two months now and haven't had such severe symptoms. I ate a couple accidents along the way but I'm doing a lot better
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