Category: Food Labels


Updated excerpt from Codex Alimentarius — The End of Health Freedom 

Available Here

 

Brandon Turbeville
Activist Post

In several of my recent articles, I have discussed the problems of using “risk assessment” methodology in the evaluation of both vitamin and mineral supplements and Genetically Modified (GM) food. I have also discussed at length the dangers of the Codex Alimentarius and U.S. Food and Drug Administration position on GM food which is known as “substantial equivalence” and, in its more extreme forms, “substantial similarity.”

However, another concern addressed by the Codex Guidelines has to deal with antibiotic resistance created through the process of genetic engineering. Yet, as is typical of any Codex Alimentarius presentation, the agency makes several misleading and unsettling statements in this regard as well. While Codex does state that methods should be used that do not result in antibiotic resistance, it qualifies that claim in its document “Foods Derived From Modern Biotechnology,” by stating that these methods should be used “where such technologies are available and demonstrated to be safe.”[1] This is certainly no mandate. It is merely a suggestion that will most likely be completely ignored by industry.

The Guidelines then go on to say that “Gene transfer from plants and their food products to gut micro-organisms or human cells is considered a rare possibility because of the many complex and unlikely events that would need to occur consecutively.”[2] This statement stands in direct contradiction to established science.[3] Indeed, the series of events that would have to transpire in order for the transfer of modified genes from a plant to human DNA or cells are neither unlikely nor rare.
In a footnote to this statement, Codex makes the claim “In cases where there are high levels of naturally occurring bacteria that are resistant to the antibiotic, the likelihood of such bacteria transferring the resistance to other bacteria will be orders of magnitude higher than the likelihood of transfer between ingested foods and bacteria.”[4] Yet while this may in fact be true the statement is still misleading. The issue being discussed in the footnoted statement is the likelihood of DNA transfer from GM plants to humans. Furthermore, if such events were so unlikely, why would it be important not to use antibiotic resistant gene technology in the future?

Another concern presented in the section of “Foods Derived From Moderin Biotechnology” dealing with GM plants is the question of potential allergens being created within the food products as well as the introduction of entirely new allergens that have never before existed in nature.

While Codex claims that “all newly expressed proteins” as well as “a protein new to the food supply” should be tested for safety, there are legitimate questions as to whether or not Codex has the ability or the desire to test for such possibilities. [5]

First, while it is quite possible to know what foods occurring naturally are allergenic, it is much more difficult to come to these conclusions about new substances or proteins. This is partly due to the fact that naturally occurring materials have so many millions of years of history and use which, in itself, tends to naturally weed out the allergenic foods from the non-allergenic ones in a population’s diet. GM products do not have this history.

Indeed, the idea that over time a population tends to form its own guidelines through natural process adds to the ease in which scientific inquiry may form knowledge of the food properties in relation to the population itself. Again, this is not the case with GM food.

Read Full Article Here

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Codex Alimentarius and GM Food Guidelines, Pt. 8

Updated excerpt from Codex Alimentarius — The End of Health Freedom

 

Available Here

 

Brandon Turbeville
Activist Post

In the course of the recent article series I have written regarding Codex Alimentarius and its position on Genetically Modified (GM) food, I have criticized both the “risk assessment” method of GM food evaluation as well as the official position of Codex Alimentarius in regards to the “substantial equivalence” standards. I have also written about the very real possibility of the introduction of new allergens and antibiotic resistant bacteria into the general food supply.

However, up to this point, all of the problems with the Codex Guidelines mentioned have been in relation to the section of the Codex GM position document known as “Foods Derived From Modern Biotechnology,” which focuses on GM plants.

There are, accordingly, two more sections – one dealing with GM Micro-Organisms and the other dealing with GM animals.

However, while it may seem that the majority of criticism expressed thus far focuses more attention on the first section (GM plants), the fact is that all three sections are very similar in their language and directives, with only a few changes in the wording made to apply to the new topic.

In many of these sections the language is word for word, copied and pasted to reiterate the same purpose as the first section. Therefore, I will not repeat my criticisms of the second and third sections that have appeared in my criticism of the GM Plants section. Suffice to say that all of the problems existing in the GM Plant section exist in the GM Micro-Organism and GM Animal sections as well, namely those of questionable scientific practices, the ignoring of relevant data, and so on. This claim is easily verifiable by reading the Guidelines document cited in the footnotes.

With that said, some attention should be paid to the section entitled, “Guideline For The Conduct Of Food Safety Assessment Of Foods Produced Using Recombinant-DNA Micro-Organisms.” This section deals mainly with bacteria, yeasts, and certain types of fungi in their uses in food production.

While making many of the same admissions present in the GM plant Guidelines, one of the most startling statements made regarding GM micro-organisms is the admission that they can in fact survive digestion.

Codex says, “In some processed foods, they [GM micro-organisms] can survive processing and ingestion and can compete and, in some cases, be retained in the intestinal environment for significant periods of time.”[1]

While this statement is not revolutionary, it is quite surprising to see it uttered by Codex Alimentarius, an organization that seems to go to great lengths to approve GM products.

Nevertheless, the fact that these micro-organisms can survive digestion is extremely important to the GMO safety debate. So are the questions of rDNA retention in the intestinal tract, the potential for changing the intestinal flora of those consuming the GM product, and the subsequent effects on the immune system.

These are all concerns that Codex tacitly admits the existence of, simply by acknowledging the need to test them.[2] Yet the tendency of GM micro-organisms to survive digestion and begin to change the makeup of the human intestines is mentioned later, in a footnote, where it is stated quite openly,

Permanent life-long colonization by ingested micro-organisms is rare. Some orally administered micro-organisms have been recovered in feces or in the colonic mucosa weeks after feeding ceased. Whether the genetically modified micro-organism is established in the gastrointestinal tract or not, the possibility remains that it might influence the microflora or the mammalian host.[3]

It should be noted that the idea that “life-long colonization by ingested micro-organisms is rare”[4] is highly contested by many independent scientists.[5] Yet, even if one were to assume the truth of Codex’s statement, the fact that it is rare means that it is still possible. More importantly, the statement admits that, even without long-term residence in the intestinal tract, there is still the distinct possibility that it will still significantly affect the intestinal flora and likewise the host itself.

Still more obviously biased concerns exist in the subsection dealing with the information that should be provided on each of the DNA modifications or micro-organisms. This information is, for the most part, very basic. It contains such data as which genes are added, the number of insertion sites, etc. However, two sources of information that are required to be included cause some concern.

The first is the inclusion of the “identification of any open reading frames within inserted DNA or created by the modifications to contiguous DNA in the chromosome or in a plasmid, including those that could result in fusion proteins.”[6]

The second is the “particular reference to any sequences known to encode, or to influence the expression of, potentially harmful functions.”[7]

Yet, both of these expressions (fusion proteins and genes that express harmful functions) are considered potentially dangerous even under the weak Codex standards. These expressions refer to the ability of some proteins to fuse with other proteins of the same and other species, mutating the DNA of the species, or forcing it to produce potentially adverse effects. Neither of these characteristics should be present in food, yet Codex mandates only that they be reported, not removed, as a result of the testing. This appears to be a continual thread of Codex’s Guidelines.

Thus, Codex continues by saying that additional information should be provided

to demonstrate whether the arrangement of the modified genetic material has been conserved or whether significant rearrangements have occurred after the introduction to the cell and propagation of the recombinant strain to the extent needed for its use(s) in food production, including those that may occur during its storage according to current techniques;[8]

as well as

to demonstrate whether deliberate modifications made to the amino acid sequence of the expressed protein result in changes in its post-translational modification or affect sites critical for its structure or function;[9]

While reporting information related to the instances above might seem like a good idea (and certainly few would argue that it isn’t), simple reporting is not enough. Indeed, these issues, as well as the others mentioned in this section of the Guidelines, are related directly to the question of the stability of genetically modified organisms. This is mentioned briefly in this section of the Guidelines, most notably in a footnote where it says,

Microbial genes are more fluid than those of higher eukaryotes; that is, the organisms grow faster, adapt to changing environments, and are more prone to change. Chromosomal rearrangements are common. The general genetic plasticity of micro-organisms may affect recombinant DNA in micro-organisms and must be considered in evaluating the stability of recombinant DNA micro-organisms.[10]

It is clear that GM organisms are often dangerously unstable. Many of them carry genes that overproduce a certain characteristic, cannot be turned off, or simply begin to change even after it has been bonded to the new strain of DNA.

Yet, with all of these admissions by Codex as to the dangers that GM micro-organisms pose to those who consume them as well as the fact that GM DNA is often unpredictable, the Codex Guidelines recommendations for testing suggest that these micro-organisms should be assessed based upon tests conducted on the conventional counterpart, not the micro-organism itself.

If tests conclude that the questionable micro-organisms are removed or rendered non-toxic in their individual and natural states, then “viability and residence of micro-organisms in the alimentary system need no examination.”[11]

Read Full Article Here

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Codex Alimentarius and GM Food Guidelines, Pt. 9

Updated excerpt from Codex Alimentarius — The End of Health Freedom 

Available Here

Brandon Turbeville
Activist Post

In my last article entitled, “Codex Alimentarius and GM Food Guidelines Pt.8”, I detailed the Codex Alimentarius position regarding Genetically Modified (GM) Micro-Organisms. Similarly, in several of the articles I have written recently, I have also discussed the Codex position on GM plants and other GM organisms.

Yet, no analysis of the Codex Alimentarius positions on GM food and/or organisms would be complete without a discussion of the Codex position on GM animals.

Indeed, the “Guideline For The Conduct Of Food Safety Assessment Of Foods Derived From Recombinant-DNA Animals,” a subsection of the Codex document “Foods Derived From Modern Biotechnology,” is as interesting for the concerns that it does not address as for the ones that it does. Largely a copied and pasted version of the two sections before it, (“Guideline for the conduct of food safety assessment of foods derived from recombinant-dna plants” and “Guideline for the conduct of food safety assessment Of foods produced using recombinant-dna micro-organisms”) the GM animal Guidelines does not address some very key issues such as:

1.) Animal welfare
2.) Ethical, moral and socio-economic aspects
3.) Environmental risks related to the environmental release of recombinant-DNA animals used in food production
4.) The safety of recombinant-DNA animals used as feed, or the safety of animals fed with feed derived from recombinant-DNA animals, plants and micro-organisms.[1]

As can be easily seen, these issues are extremely important in their own right. Just the moral issues, in addition to the hazards of the potential of GM animals being released into the environment, are enough to fill volumes. However, Codex chooses not to deal with these issues in its Guidelines.
With that being said, because Codex treats GM animals essentially the same as GM plants, there is very little difference in the guidelines. This shows a lack of scientific zeal as animals are fundamentally different than plants.

Yet one area where Codex does address a different aspect of the GM safety question is related to veterinary drug residues. It says,

Some recombinant-DNA animals may exhibit traits that may result in the potential for altered accumulation or distribution of xenobiotics (e.g. veterinary drug residues, metals), which may affect food safety. Similarly, the potential for altered colonization by and shedding of human pathogens or new symbiosis with toxin-producing organisms in the recombinant-DNA animal could have an effect on food safety.[2]

With its implicit admission of the instability of modified genes, Codex now also admits that these genes, when changed in animals, could affect the distribution and retention of veterinary drugs and other substances which would necessarily change the content of the food product derived from that animal. As Codex states, this same situation could also apply to human pathogens as well as veterinary drugs.

As a side note, it appears that 2007-2008 was a very beneficial year for GMO food producers. Not only were the pro-GM testing Guidelines approved by Codex, but many countries, such as the European Union who had been opposed to the introduction of GM food up to this point, began changing their position to one that was slightly more open to GMO.

For instance, in 2008, Codex Alimentarius approved Guidelines that would allow low levels of GM products that have not been approved by the countries’ regulatory agencies inside products that are imported into the country. This would include products like grain, corn, and oats. Codex claims that this set of standards merely recognizes the fact that GM products will inadvertently mix with non-GM products during processing and transportation and that it means to provide guidance in this unavoidable situation.[3]

However, this presupposes that GM contamination of food shipments is unavoidable when in fact just the opposite is the case. If GM products were not used to begin with, the entire issue would not need to be addressed.

Read Full Article Here

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Updated excerpt from Codex Alimentarius — The End of Health Freedom 

Available Here

Brandon Turbeville
Activist Post

In my last article regarding Codex Alimentarius Guidelines on Genetically Modified food, I discussed the dangerous concept used by both the international organization and the U.S. Food and Drug Administration (FDA) known as substantial equivalence/substantial similarity and how this method of comparison and evaluation can and is being used to further the proliferation of GM food in the world’s food supply.

In discussing the method used to evaluate the safety of GM food, I wrote,

If Codex is willing to accept the safety assessments of regulatory agencies without independent testing of its own and regulatory agencies are willing to accept the safety assessments of corporations without independent testing of their own, then Codex is willing to accept the safety assessments of corporations without independent safety testing of their own. Indeed, this syllogism adequately reflects the reality of the relationship between Codex, corporations, and the future of GM foods.

Furthermore, in regards to the “substantial equivalence” methodology mentioned above, I concluded the article by stating,

Allowing GM products to be compared to other GM products for substantial equivalence is an enormous blow to the environment, human health, and consumer choice. Such an action would completely undercut the already weak and ridiculous method of substantial equivalence and would turn the entire nature of our food supply upside down. One would be comparing a dangerous product to another dangerous product but labeling it safe because it was substantially equivalent to the first dangerous product.

Like the situation involving vitamins and minerals, this is the Twilight Zone reality produced by Codex once it gains power of the food supply.

Unfortunately, this potential concern is now an imminent one because Monsanto has in fact submitted an application for a GM corn called LY038. In its submission for approval, Monsanto provided the regulators’ assessing the product with information comparing LY038 with another GM corn product called LY038 (-), another GM corn product.[1]
True to form, in many of the pro-GM countries such as New Zealand, Australia, Japan, Canada, the Philippines, and South Korea, the LY038 corn was approved based upon the method of using a GM corn as a conventional counterpart.[2] The United States, being the most open to GM food, and only requiring voluntary submission, has also approved LY038 for cultivation.[3]

Thankfully, the Monsanto agenda stalled in the European Union, and in 2009 Monsanto withdrew its application for the product in Europe.[4] This is largely due to a small group of relatively independent scientists from the Centre for Integrated Research in Biosafety (INBI) out of New Zealand who brought out many risks evident from a close reading of the Monsanto application dossiers.

As a result of their work, the European Food Safety Authority (EFSA) requested additional research and safety data. That was all that was needed in order to cause Monsanto to withdraw its application for LY038 use in Europe.[5]

Monsanto claimed that the reason for the removal of its submission purely economical and that “although our preference would have been to complete the EU approval of LY038, conducting further studies, as requested [by the EFSA GMO Panel], can no longer be justified, in view of the additional costs involved and the reduced commercial interest in this product.”[6]

However, those who are aware of Monsanto’s track record have a different take. In a statement made to Biosafety Information Centre, Prof. Jack Heinemann, who led the INBI research team, summed up the situation succinctly.

 

Read Full Article Here

March 7, 2013 by APRIL McCARTHY

Prevent Disease .com

The modern diet of processed foods, takeaways and microwave meals could be to blame for a sharp increase in autoimmune diseases such as multiple sclerosis, including alopecia, asthma and eczema.

A team of scientists from Yale University in the U.S and the University of Erlangen-Nuremberg, in Germany, say junk food diets could be partly to blame.

‘This study is the first to indicate that excess refined and processed salt may be one of the environmental factors driving the increased incidence of autoimmune diseases,’ they said.

Junk foods at fast food restaurants as well as processed foods at grocery retailers represent the largest sources of sodium intake from refined salts.

The Canadian Medical Association Journal sent out an international team of researchers to compare the salt content of 2,124 items from fast food establishments such as Burger King, Domino’s Pizza, Kentucky Fried Chicken, McDonald’s, Pizza Hut and Subway. They found that the average salt content varied between companies and between the same products sold in different countries.

U.S. fast foods are often more than twice as salt-laden as those of other countries. While government-led public health campaigns and legislation efforts have reduced refined salt levels in many countries, the U.S. government has been reluctant to press the issue. That’s left fast-food companies free to go salt crazy, says Norm Campbell, M.D., one of the study authors and a blood-pressure specialist at the University of Calgary.

Many low-fat foods rely on salt–and lots of it–for their flavor. One packet of KFC’s Marzetti Light Italian Dressing might only have 15 calories and 0.5 grams fat, but it also has 510 mg sodium–about 1.5 times as much as one Original Recipe chicken drumstick. (Feel like you’re having too much of a good thing? You probably are.

Bread is the No. 1 source of refined salt consumption in the American diet, according to the Centers for Disease Control and Prevention. Just one 6-inch Roasted Garlic loaf from Subway–just the bread, no meat, no cheeses, no nothing–has 1,260 mg sodium, about as much as 14 strips of bacon.

How Refined Salt Causes Autoimmune Disease

The team from Yale University studied the role of T helper cells in the body. These activate and ‘help’ other cells to fight dangerous pathogens such as bacteria or viruses and battle infections.
Previous research suggests that a subset of these cells – known as Th17 cells – also play an important role in the development of autoimmune diseases.

In the latest study, scientists discovered that exposing these cells in a lab to a table salt solution made them act more ‘aggressively.’

They found that mice fed a diet high in refined salts saw a dramatic increase in the number of Th17 cells in their nervous systems that promoted inflammation.

They were also more likely to develop a severe form of a disease associated with multiple sclerosis in humans.

The scientists then conducted a closer examination of these effects at a molecular level.

Laboratory tests revealed that salt exposure increased the levels of cytokines released by Th17 cells 10 times more than usual. Cytokines are proteins used to pass messages between cells.

Study co-author Ralf Linker, from the University of Erlangen-Nuremberg, said: ‘These findings are an important contribution to the understanding of multiple sclerosis and may offer new targets for a better treatment of the disease, for which at present there is no cure.’

 

Read Full Article Here


breakingtheset

Published on Feb 28, 2013

Abby Martin breaks the set on Food Safety, Hactivist Barrett Brown, and Japanese Internment Camps.

EPISODE BREAKDOWN: On this episode of Breaking the Set, Abby Martin talks to Jaydee Hanson, Policy Analyst for the Center for Food Safety, about finds of horse meat in the UK, and what this says about the potential for food fraud in the US. Abby then talks to Christian Stork of WhoWhatWhy.org about the case of online activist, Barrett Brown, and US government’s fixation on preemptive prosecution of anyone exposing government wrongdoing. BTS wraps up the show with a look the 71st anniversary of the internment of Japanese people in the US following the attack on Pearl Harbor, and how the growing surveillance state is the modern day internment camp.

Excitotoxins, as they are appropriately named, are supposed to enhance flavor and excite your taste buds, but this “class” of chemicals overstimulate neuron receptors, which are what allow brain cells to communicate with each other. This causes a firing of impulses atsuch a rapid rate that they become completely exhausted, and several hours later, these depleted neurons die. This is true cell death, and the parts of the brain that are specifically targeted by excitotoxins are the hypothalamus and temporal lobes, which not only control behavior, emotions, and sleep cycles, but you guessed it, immunity. (http://experiencelife.com/article/excitotoxins/)

Aspartame and MSG stimulate the taste cells in the tongue, causing food flavor to be enhanced, especially in soups, snacks, sauces, gravies, low-fat processed foods, and now aspartame is found in 95 percent of breath mints and chewing gum, even when they’re not “sugar free.” If you regularly experience any or all of the following, it’s about time to question the amount of “excitotoxins” that are swimming through your heart and brain. Do you suffer from migraine headaches, inflammation, unwarranted weight gain, rashes and “crawling skin?” It may all be spurred by genetically modified flavor enhancers.

Let’s cover all of the bases. Monosodium glutamate (MSG) has at least 20 different names. There are many other products/additives that are simply “sisters” or “cousins” of MSG, but beware, because MSG is amacro-combination of these other “food” additives and chemically engineered flavor enhancers. Plus, the MSG “cousin” additives do not have to be labeled as MSG because they are not manufactured in tandem, so when enough of them add up in your daily intake, you may as well have eaten MSG on an empty stomach.
(http://www.truthinlabeling.org/Proof_BrainLesions_CNS.html)

How do you avoid MSG, aspartame and their criminal cousins?

Stop buying and stop consuming the following: Glutamic acid, glutamate, monopotassium glutamate, calcium glutamate, autolyzed yeast, calcium caseinate, gelatin, anything “hydrolyzed,” sodium caseinate, soy protein, soy protein concentrate, soy protein isolate, textured protein, whey protein, whey protein concentrate, whey protein isolate, yeast extract, yeast food, and yeast nutrient. (http://copingwithmsg.blogspot.com)

Warning: don’t be fooled by “Pro-MSG” websites that state MSG is an amino acid that the “body produces on its own,” because the MSG on store shelves is processed, GMO and comes from fermented sugar beets. That’s why Monsanto has a monopoly on sugar beets. Watch out for glutamic acid and its ions and salts called glutamates, which are compounds found in many fermented foods, including soy sauce, cheese and hydrolyzed protein.
(http://en.wikipedia.org/wiki/Glutamic_acid_(flavor))

MSG is the leading cause of migraine headaches, which result from a blood vessel enlargement and the release of chemicals from nerve fibers that coil around these vessels. During the headache, an artery enlarges outside the skull, but just under the skin (the temple). This is when the warning signs that you’ve consumed MSG ring out, and many people experience flashes of light, blind spots, tingling in the arms and legs, nausea, vomiting, and increased sensitivity to light and sound. The pain becomes so excruciating, it’s almost unbearable. Some migraines are known to last for days. Could that be because the medicine you take contains more?
(http://www.naturalnews.com/029119_migraine_headaches_foods.html)

The “K” criminal “Acesulfame K” creates “significant doubt”

Chemical sweeteners should be entirely avoided by all human beings at all times and you have to know their “hiding places” in order to keep them out of your body. Acesulfame K is just a cousin of aspartame, so don’t be fooled by the label. Acesulfame Potassium (K) was approved for use by the FDA in July of 1988. It is a derivative of acetoacetic acid. Several animal studies/findings show the following: Acesulfame K stimulates insulin secretion in a dose dependent fashion thereby possibly aggravating reactive hypoglycemia (low blood sugar attacks). Acesulfame K produced lung tumors, breast tumors, and several forms of leukemia and chronic respiratory disease in rodent studies, even when less than maximum doses were given. Still, the FDA eliminated “significant doubt” about its safety and kept it on the shelves. (http://www.sweetpoison.com/aspartame-sweeteners.html)

asparatame

Aspartame was banned for decades in the U.S. until 1980, when Ronald Reagan and the infamous Donald Rumsfeld fired the head of the FDA and hired Arthur Hayes Hull, Jr., who immediately approved aspartame (http://www.nndb.com/people/634/000023565/). Hull later left the FDA under allegations of impropriety and then took a position with Burston-Marsteller, the chief public relations firm for both Monsanto and GD Searle. Since that time, he has never spoken publicly about aspartame. Nobody wonders why.

 

Read Full Article Here

 

Czech Republic officials say traces of horse meat were discovered in frozen packages of meatballs sent to their country for sale at furniture giant Ikea. NBCNews.com’s Dara Brown reports.

By Juergen Baetz and Karel Janicek, The Associated Press

Traces of horse have been found in meatballs labeled as beef and pork for Swedish global furniture giant Ikea, according to authorities in the Czech Republic.

The horse meat was found in one-kilogram packs of frozen meat balls made in Sweden and shipped to the Czech Republic for sale in Ikea stores there, the Czech State Veterinary Administration said.

It is the latest discovery in a deepening scandal over the discovery of horse meat in ready meals sold as beef in supermarkets in Ireland, the UK and other European countries.

Markus Schreiber / AP, file

Ikea furniture stores also sell typical Swedish food.

A total of 1,675 pounds of the meatballs were stopped from reaching the shelves.

Ikea’s furniture stores feature restaurants and also sell food typical of the company’s home country, including the so-called Kottbullar meat balls.

It was not immediately clear whether Ikea exported the same product to other countries. Calls seeking comment from Ikea in Sweden were not immediately returned Monday.

The Czech authority also found horse meat in beef burgers imported from Poland during random tests of food products.

Authorities across Europe have started doing random DNA checks after traces of horse meat turned up in frozen supermarket meals such as burgers and lasagna beginning last month.

 

Read Full Article  and Watch Video Here

Activist Post

Two powerful dairy organizations, The International Dairy Foods Association (IDFA) and the National Milk Producers Federation (NMPF), are petitioning the Food and Drug Administration to allow aspartame and other artificial sweeteners to be added to milk and other dairy products without a label.

The FDA currently allows the dairy industry to use “nutritive sweeteners” including sugar and high fructose corn syrup in many of their products. Nutritive sweeteners are defined as sweeteners with calories.

This petition officially seeks to amend the standard of identification for milk, cream, and 17 other dairy products like yogurt, sweetened condensed milk, sour cream, and others to provide for the use of any “safe and suitable sweetener” on the market.

They claim that aspartame and other artificial sweeteners would promote healthy eating and is good for school children.

According to the FDA notice issued this week:

IDFA and NMPF state that the proposed amendments would promote more healthful eating practices and reduce childhood obesity by providing for lower-calorie flavored milk products. They state that lower-calorie flavored milk would particularly benefit school children who, according to IDFA and NMPF, are more inclined to drink flavored milk than unflavored milk at school.

Read Full Article Here

Mikael Thalen, Contributor
Activist Post

Washington state recently made national news after the “Label It Wa” grassroots campaign successfully collected and submitted over 350,000 signatures in order to get “I-522 The People’s Right to Know Genetically Engineered Food Act” on the 2013 ballot. This bill would require genetically engineered food in the state to be labeled.

Also in Washington, San Juan County residents and farmers passed Initiative Measure No. 2012-4 to ban the growth of genetically modified organisms. Now, Republican Representative Cary Condotta has stepped up and introduced House Bill 1407, which aims to remove the bureaucratic red tape, allowing local legislative authorities to regulate genetically modified organisms from foods to seeds as they see fit, instead of relying on the state to take action.

“When we saw San Juan do this, we thought it was great, so we see this on a different path than I-522 but we made sure to put a provision in HB 1407 that none of it would override I-522, so if the labeling bill passes all food will still be labeled state wide still, this just gives the local level even more control,” explained Rep Condotta.

 

Read Full Article Here

The Raw Story
Thu, 24 Jan 2013 12:21 CST

© AFP Photo

Burger King has ditched an Irish supplier of beef that is at the centre of a food scare after horse meat was discovered in beefburgers sold in Britain and Ireland, where it is deemed to be a taboo.

The US fast-food giant said Wednesday it has decided to replace all Silvercrest beef products in Britain and Ireland with those from another supplier.

“This is a voluntary and precautionary measure,” Burger King said in a statement.

“We are working diligently to identify suppliers that can produce 100 percent pure Irish and British beef products that meet our high quality standards.”

 

Read Full Article Here

Would you eat biotech fish? FDA approves genetically engineered salmon

 

by: Raw Michelle

 

(NaturalNews)The FDA added that it would take public comments for 60 days before finally deciding on whether or not to approve the salmon.

Criticism of the recent FDA assessment points to the lack of sufficient evidence that the fish is safe for consumption, and the difficulty in measuring its real impact on the environment once mass production begins.

Where does biotech salmon come from?

The controversial fish is developed by AquaBounty Technologies, a small American biotechnology company whose main goal is to find solutions that could increase the productivity of aquaculture. Its most important research consists of developing salmon, trout, and tilapia eggs that produce fast growing specimens. To achieve this, researchers have to modify the very genetic fabric of fish. Their salmon variety has been patented and bears the trade name AquAdvantage Salmon.

The FDA report so far states that “with respect to food safety, FDA has concluded that food from AquAdvantage salmon is as safe as food from conventional Atlantic salmon, and that there is a reasonable certainty of no harm from consumption.”

What the critics say

Michael Hansen, a researcher at the Consumers Union, explained that GE fish could cause allergic reactions that the FDA is unable to anticipate. GE fish will also likely not be labeled accordingly, leaving consumers in the dark about where the fish is coming from.

If the FDA does not heed the public outcry, Congress could still prevent the commercialization of GE fish. Wenonah Hauter, director at the Food & Water Watch, urges consumers to contact their congressmen to overturn what has been called “a dangerous experiment” at the expense of consumer health.

Other concerns about GE fish pertain to its ability to outcompete natural Atlantic salmon. If it is released into the wild, the AquAdvantage salmon could adapt to new pray, survive in tough habitats, and reproduce much faster than its natural counterpart.

Andrew Kimbrell of the Center for Food Safety concluded that “the GE salmon has no socially redeeming value. It’s bad for the consumer, bad for the salmon industry and bad for the environment.”

Healthy, vegan alternatives to GE salmon

Chickpeas have been hailed by vegans everywhere for their ability to mimic fish, making them an excellent addition to faux fish salads. Chickpeas provide considerable amounts of protein, slow release carbohydrates, folate and zinc.

A delicious vegan “salmon” dish can be prepared by mixing grated carrots, mashed chickpeas, white vinegar, tomatoes, finely grated lemon peel, lemon juice, dill, vegetable oil and a pinch of salt. The mixture can either be consumed raw, or divided into patties and baked for about 25 minutes. For added flavor, vegan “salmon” can be topped with vegan mayonnaise or grated horseradish.

When choosing salmon as a means to obtain healthy fats, many may want to consider chia instead. With 724 mg of Omega-3′s in 28 grams of salmon, and 4915 mg in 28 grams of chia, chia is a clear winner.

Sources for this article include:
http://www.reuters.com
http://www.fda.gov
http://www.guardian.co.uk
http://www.onegreenplanet.org/vegan-food/recipe-vegan-salmon-patties/
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About the author:
Raw Michelle is a natural health blogger and researcher, sharing her passions with others, using the Internet as her medium. She discusses topics in a straight forward way in hopes to help people from all walks of life achieve optimal health and well-being. She has authored and published hundreds of articles on topics such as the raw food diet and green living in general. In 2010, Michelle created RawFoodHealthWatch.com, to share with people her approach to the raw food diet and detoxification.

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