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wowzer Community Regular

Seventh Generation Non-Toxic Times. We thought we


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debmidge Rising Star

Now that you mention it, last week I heard on Radio that Philip Morris will be selling the "Kraft" product line off.

blueeyedmanda Community Regular

Philip Morris as in the cigarette company?? I never knew that, interesting. Disturbing...but interesting.

jerseyangel Proficient

That was interesting. Thanks for taking the time to post it :)

gfp Enthusiast
Philip Morris as in the cigarette company?? I never knew that, interesting. Disturbing...but interesting.

That part I find less disturbing..

The part to worry about is when gaint corps are just making a brandname that caters for a "health segment" of the market.

In-most cases this is simply a marketing ploy, a while back I posted the published minutes from a food industry meeting where several multinationals identified a need for food that is perceived as healthy.. and I highlight that word specifically.

In no case I can think of does a multinational actually care about your health so long as you are well enough to get out of the house and buy thier products off the shelf. They only case about your custom...

The real worry is that these companies are only interested in what is perceived as healthy and catering to fads.

If gluten-free is trendy they will market to it but if that means filling out their product with other alergens then I doubt they think that will influence sales overtly.

In many cases the mutlinationals have lots of spare byproducts to use... often byproducts which are taken out of heaviliy processed foods (or in this case cigarettes).... and whenever they can they will use these byproducts as a product line.

Thus if you produce lots of white bread, process lots of rice to white rice then you have lots of fibre left over to use. A healthfood subsidiary is ideal to get rid of these waste products.... (in the case of Philip Morris this is nicotine gum and similar which in some studies (not the ones paid for by Phillip Morris) is proven to have a higher failure rate than cold turkey)

The same goes equally for food if less transparently...

Soy is in public opinion associated with healthy eating... along with whole grain breads etc. anything based on seaweed or other nice buizzwords....

In general when you read the labels on some so called "health products" it sounds like a list of byproducts... chosen because they sound healthy or even just renaming neutral products like "aqua" instead of just saying water...

One thing disturbs me is that although I'm not anti-soy in general I don't want it making up a significant part of my diet, it seems OK for me but many celiacs including my mother do react badly to it and IMHO eating significant amounts of it is the best way to develop a future intolerence.

But there is no need for everyone to wear tin hats... I think its pretty easy to read the labels and decide... if it contains things you don't know what they are or shouldn't be in the product to start with the chance is they are not going to be good, regardless of the big label saying "Healthy options/alternatives/etc.)

A good example is gluten-free pasta... my usualyl fav is "corn, water" .or vermicelli type "Rice, water" .. if the list gets any longer chance is whatever is added isn't good!

tummytroubles Newbie

Thanks for all of the information. Its pretty scary! I'm definitely going to be more careful when selecting prepackaged food labeled "healthy".

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    • captaincrab55
      Welcome sillyyak52,  I'm not sure of your age or if you live with your parents.  Is there a nurse in your family or friend of the family that may be able to explain your diagnoses?  You can get a second opinion by taking your lab results to another GI Doctor.   Good Luck!
    • trents
      So, you have three symptoms of a gluten-related disorder: weight loss, brain fog and lose stools. Of the three, the lose stools that firm up when you cut back on gluten is the only symptom for which you have reasonable cause to assume is connected to gluten consumption since the other two persist when you cut back on gluten. But since you do not have any formal test results that prove celiac disease, you could just as easily have NCGS (Non Celiac Gluten Sensitivity). In fact, what testing you have had done indicates you do not have celiac disease. NCGS shares many of the same symptoms of celiac disease but does not damage the lining of the small bowel as does celiac disease. There is no test for it. A diagnosis for NCGS depends on first ruling out celiac disease. It is 10x more common than celiac disease. Some experts feel it can be a precursor to the development of celiac disease. Eliminating gluten is the antidote for both. What muddies this whole question are two things: 1. Lack of official diagnostic data that indicates celiac disease. 2. Your persistence in consuming gluten, even though in smaller amounts. Your anxiety over the insomnia seems to outweigh your anxiety over the weight loss which prevents you from truly testing out the gluten free diet. What other medical testing have you had done recently? I think something else is going on besides a gluten disorder. Have you had a recent CBC (Complete Blood Count) and a recent CMP (Complete Metabolic Panel)? You say you don't believe you have any vitamin and mineral deficiencies but have you actually been tested for any. I certainly would be concerned with that if I was losing weight like you are despite consuming the high amount of calories you are.
    • trents
      Welcome to the forum, @AndiOgris! Recently upgraded guidelines for the "gluten challenge" recommend the daily consumption of at least 10g of gluten for at least 2 weeks to the day of testing to ensure valid testing, either for the antibody testing or the endoscopy/biopsy. 10g of gluten is roughly the amount found in 4-6 slices of wheat bread. So, there is a question in my mind as to whether or not your gluten consumption was intense enough to ensure valid testing the second time around. And was the tTG-IGA the only antibody test that was run? That is far from a comprehensive celiac panel. Concerning your negative biopsy, there is the possibility of patchy damage that was missed due to inadequate sampling as you alluded to. There is also the possibility that the onset of your celiac disease (if you have it) was so new that there had not yet been time to accumulate damage to the small bowel lining. Your total lack of symptoms at the time of diagnosis would seem to support this idea. Having said all that, and this is my informal observation from reading many, many posts like yours over the years, I wonder if you are on the cusp of celiac disease, crossing back and forth across that line for the time being. My suggestion would be to keep a close eye on this for the time being. Watch for the development of symptoms and request a more complete celiac panel a year from now. Here is an article that discusses the various antibody tests that can be run for celiac disease. Note: The EMA test is kind of outdated and expensive. It has been replaced by the tTG-IGA which measures the same thing and is less expensive to run.  
    • SaiP
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    • AndiOgris
      Hi all I have had a very confusing year with celiac disease (or perhaps not as it turns out) and wondered if anyone can help me make sense of it? My mother was diagnosed with celiac disease (in her 70s) a couple of years ago. I am in my early 40s and did not have any symptoms, but I took a blood test in November 2023 and it came back positive (TTG IGA 23.4 U/ml - normal range is below 7 U/ml). I was referred for a gastroscopy to confirm, which was scheduled for October 2024 (I use the UK health service, things move slowly!). The gastroscopy found no evidence of celiac disease.  My gastroenterologist has asked me to retake the blood test, and it just came back negative (TTG IGA 1.6 U/ml - normal range is below 7 U/ml). Given the long wait between my initial positive blood test and my gastroscopy, I reduced my gluten intake but never avoided it fully. In the 6 weeks before the gastroscopy and the second blood test, I made sure to eat at least two slices of bread a day as recommended, and often I had significantly more.  So what's going on? I understand that false positives are very rare for celiac blood tests, and usually associated with other serious diseases which I am fairly sure I don't have (my health is generally very good). After the negative biopsy, I thought that (i) either they did not take enough samples, or (ii) I have "potential celiac disease". But now that the second blood test has come back negative, I'm running out of plausible explanations...  Can anyone make sense of this? I have not spoken to my gastroenterologist yet - I wanted to get a better sense of where I am beforehand so that I can ask the right questions. Under the UK system, specialist doctors can be very hard to get hold of, so I need to make the most of my time with him! Thanks!        
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