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New To gluten-free Forum...and Celiacs!


Amz17

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Amz17 Newbie

Hey everyone!

:rolleyes:

I have searched all over the internet for a decent forum, until i found this one. I was recently diagnosed with a weak positive celiacs disease result, and am finding it hard to find gluten-free foods as i live in such a small town. I discovered a gluten-free food ordering site, but its hard to order things without looking at the food. I am also not sure if i have to be on a long-term diet, or short-term because of only have a weak positive result. My doctors appointment is next week which was the soonest i could get in. After that i will hopefully know more about my diet and stuff. But if anyone else knows how long the diet would be for a weak positive result...i would love to hear from you! Any interesting and useful information would be greatly appreciated too. I search the internet for information, but its not very informative, unless I compile 50 pages and get the main points! I hate reading a whole heap of information and only finding 3 useful things! Anyway, I best go and do something useful! :P

Email me if you want...scalywag_69@hotmail.com

- Amber xxx


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flagbabyds Collaborator

Any positive number in your blood tests means that you are going to be on this diet for life. SORRY!

I know it must seem like that sucks so much right now, but it will get better, I promise.

I must go to sleep, but if you have any quesetions email me @ celiacmolly08@mac.com or send me an IM missmolly3001

tarnalberry Community Regular

if you're positive, you're positive, and it's important to remain gluten-free permanently. while it may be hard at the moment to find specialty items and gluten free packaged/processed items, your local grocery store still has lots of food you can eat - produce, meat, rice, beans, dairy, eggs. you can cook almost anything from these items. start simple, keeping to foods that are naturally gluten free, and expand from there. it is a major transition, but one that will make you healthier.

Amz17 Newbie

Is maltodextrin derived from corn or wheat? Im confused! :blink:

nettiebeads Apprentice
Is maltodextrin derived from corn or wheat? Im confused! :blink:

I've read that in the US, it's from corn unless otherwise stated.

celiac3270 Collaborator

In medication, you need to check maltodextrin.

In food, in the U.S., maltodextrin is made from corn unless it specifically states "wheat maltodextrin."

Amz17 Newbie

What about in australia?


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    • knitty kitty
      @rei.b,  I understand how frustrating starting a new way of eating can be.  I tried all sorts of gluten-free processed foods and just kept feeling worse.  My health didn't improve until I started the low histamine AIP diet.  It makes a big difference.   Gluten fits into opioid receptors in our bodies.  So, removing gluten can cause withdrawal symptoms and reveals the underlying discomfort.  SIBO can cause digestive symptoms.  SIBO can prevent vitamins from being absorbed by the intestines.  Thiamine insufficiency causes Gastrointestinal Beriberi (bloating, abdominal pain, nausea, diarrhea or constipation).  Thiamine is the B vitamin that runs out first because it can only be stored for two weeks.  We need more thiamine when we're sick or under emotional stress.  Gastric Beriberi is under recognised by doctors.  An Erythrocyte Transketolace Activity test is more accurate than a blood test for thiamine deficiency, but the best way to see if you're low in thiamine is to take it and look for health improvement.  Don't take Thiamine Mononitrate because the body can't utilize it well.  Try Benfotiamine.  Thiamine is water soluble, nontoxic and safe even at high doses.  I thought it was crazy, too, but simple vitamins and minerals are important.  The eight B vitamins work together, so a B Complex, Benfotiamine,  magnesium and Vitamin D really helped get my body to start healing, along with the AIP diet.  Once you heal, you add foods back in, so the AIP diet is worth doing for a few months. I do hope you'll consider the AIP diet and Benfotiamine.
    • 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
      I was tested for celiac at the same time, so I wasn't taking naltrexone yet. I say that, because I don't. The endoscopy showed some mild inflammation but was inconclusive as to celiac disease. They took several biopsies and that's all that was shown. I was not given a Marsh score.
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