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Silly Question


mammajamma

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mammajamma Rookie

Hi everybody... I am new to the forum, was just finally offically diagnosed the other day. My 9 year old daughter will be having her upper endoscopy this week and I am expecting the same results. Anyway, since I am brand new, I've been reading lots of posts and am wondering... what does CC mean??? I have not come across that term before...


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Aleshia Contributor
Hi everybody... I am new to the forum, was just finally offically diagnosed the other day. My 9 year old daughter will be having her upper endoscopy this week and I am expecting the same results. Anyway, since I am brand new, I've been reading lots of posts and am wondering... what does CC mean??? I have not come across that term before...

I'm pretty new too and just figured it out yesterday CC="cross contamination"

mamaw Community Regular

CC is cross- contamination. hth

mammajamma Rookie

thanks guys! I can see that I am really in for an adventure. I am glad to find this forum for support and as a source for information... but I have to tell you, it's also scaring the heck out of me! I'm thinking "we'll just cut out the gluten and everything will be fine" and now I'm reading about buying all new cookware... getting sick from just HANDLING other people's food... I've gotta tell you, I am REALLY nervous now!!! :(

kevsmom Contributor

There are no silly questions ;) - Ask away, someone is always here to help. You are not alone.

Cindy

mammajamma Rookie

Thanks, Kevsmom... I appeciate that... feeling a little overwhelmed lately, between me and my daughter... :(

Darn210 Enthusiast
thanks guys! I can see that I am really in for an adventure. I am glad to find this forum for support and as a source for information... but I have to tell you, it's also scaring the heck out of me! I'm thinking "we'll just cut out the gluten and everything will be fine" and now I'm reading about buying all new cookware... getting sick from just HANDLING other people's food... I've gotta tell you, I am REALLY nervous now!!! :(

It seems overwhelming at first, but you'll get the hang of it pretty quickly. I can't believe my daughter has been gluten-free for over a year now. I know that we started out with a somewhat limited but safe repertoire of food. Then gradually added (or rather modified our old family favourites) and have greatly expanded our meal options.

You don't necessarily need to buy new cookware. You need to replace scratched up nonstick cookware, otherwise, just give your metal pots and pans a good scrub down. You need to get a new toaster, cutting board, and strainer. Throw out your wooden utensils. If the whole house is not going gluten-free, you need to have separate butters, peanut butters, jellys, etc . . . anything that you dip your knife into and can transfer crumbs to. You'll make mistakes and you'll learn from them. We all do.

There is a wealth of information and lots of people to help in this forum just ask.


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    • DebJ14
      Migraines ran in my family, on my father's side.  All of my female first cousins on that side, and our grandmother suffered from Migraines.  Grandmother died in 1984 so we do not know if she ever would have been diagnosed with celiac disease. However, all 4 of us cousins were diagnosed with celiac disease between 2003 and 2007.  The dermatitis herpetiformis rash is a blistery, super itchy rash.  When they do the biopsy they take it from non-involved skin that is next to the rash.  If done wrong, the results may not be accurate.  Have you ever had one done? In that case, I agree that maybe she has you still on gluten for a biopsy.  But, if she has not ordered it nor referred you to a gastroenterologist, then I would question her advice.  
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    • Scott Adams
      It's possible that your doctor wants you to do an endoscopy to confirm the diagnosis, and if that is the case that could be why they don't want you to go gluten-free before that procedure is done.  Here is more info about how to do a gluten challenge for a celiac disease blood panel, or for an endoscopy: and this recent study recommends 4-6 slices of wheat bread per day:    
    • NCalvo822
      Hi! Your history is interesting as I see parallels with my history. I too had migraines since childhood, but they run in my family so I didn’t think there could be any connection to the celiac. Also, the migraines have tapered off after menopause. I too have trouble walking in a straight line. And yet another similarity is I have been seeing both a dermatologist and an allergist for many years. The allergist has run many tests for my skin issues, but concluded I am not allergic to anything. I do occasionally get hives and am on daily medication to control the hives and other rashes or similar issues. At my last appt with allergist recently, I informed them of my new diagnosis of celiac disease. They said that it has nothing to do with my skin issues. They didn’t even put it in my chart. I know because I read the notes from the visit on the patient portal. However, your post has me second guessing my skin issues and possible connection to celiac disease.
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