MONSANTO'S MUTATED WORLD AND THE FDA'S HUMAN EXPERIMENT.
Posted Oct 28 2009 11:02pm
MONSANTO'S MUTATED WORLD AND THE FDA'S HUMAN EXPERIMENT.
By Byron J. Richards, CCN October 28, 2009 NewsWithViews.com
America’s sugar crop is under GMO assault and the FDA has begun a new era of human experimentation. America is in dire need of a new super hero – and he has arrived. It is Larry Leptin, defending your right to be healthy.
See Larry Leptin’s first episode: Halloween fun as he takes on the GMO mutated sugar beets.
Monsanto’s Toxic and Mutated World – Is Sugar Safe to Eat?
It should come as no surprise when a Monsanto product poisons the earth and our food. Our planet has never recovered from the forty-year Monsanto-led PCB contamination that was banned in the U.S. in 1977. To this day environmental PCBs continue to degrade into highly toxic furans and dioxins, wreaking all manner of human health problem. The new case in point involves several aspects: 1) the bizarre alteration of the nature of food itself by splicing viral, bacterial, and other life forms into the DNA of food (GMO seeds and crops), and 2) the massive increase in the use of glyphosate pesticide (Round Up), which is polluting the water, soil, and food across the globe. Both issues are extremely problematic to human health.
On September 21, 2009 a stunning shot was fired across the bow of Monsanto and its new legion of Frankenfood sugar beet growers. Judge Jeffrey S. White of Federal District Court in San Francisco said the Agriculture Department should have done an environmental impact statement as required by law. He said it should have assessed the consequences from the likely spread of the genetically engineered trait to other sugar beets or to the related crops of Swiss chard and red table beets. He said that the potential elimination of farmer’s choice to grow non-genetically engineered crops, or a consumer’s choice to eat non-genetically engineered food constituted a significant effect on the environment that necessitated an environmental impact statement. The case is ongoing, with the next phase scheduled for October 30.
Meanwhile, Monsanto is attempting damage control during the second growing season of this genetic monstrosity masquerading as food. The judge hasn’t banned the current year’s crop or the sale of Halloween candy which is now full of GMO sugar. Of course, GMO sugar, like other GMO “foods,” doesn’t need to be labeled as such (because nobody in their right mind would buy it if it were). Half the refined sugar in the U.S. is from beets – and insiders say the industry has quickly converted to the GMO Frankenfood beets, estimating up to 95% of farmers are now using them.
Beet sugar is often mixed with cane sugar, meaning that unless a product lists the ingredient as cane sugar or organic cane sugar then it now likely contains GMO mutant beet-derived sugar.
Only the biotech industry and its financially-associated friends believe GMO Frankenfoods are safe to eat. The despicable management at the FDA approved them, while squashing and hiding from public view the numerous safety objections of their scientific staff. Common sense will tell virtually anyone that having foreign organism DNA spliced into the essence of food is an atrocity.
Earlier this year the American Academy of Environmental Medicine (AAEM) called on physicians to educate their patients, the medical community, and the public to avoid genetically modified foods and provide educational materials concerning GM foods and health risks. They called for a moratorium on GM foods, long-term independent studies, and labeling. AAEM’s position paper stated, “Several animal studies indicate serious health risks associated with GM food, including infertility, immune problems, accelerated aging, insulin regulation, and changes in major organs and the gastrointestinal system…There is more than a casual association between GM foods and adverse health effects. There is causation.”
All of these Round Up ready Frankenfood crops are leading to unprecedented use of Round Up (glyphosate). In 1994 glyphosate pesticide use was 7.9 million pounds. By 2005, with the widespread use of Round Up, that number jumped to 119.1 million pounds. This is breeding super weeds that require ever increasing amounts of Round Up, not to mention other new “super toxic” pesticides just to keep up with the war on weeds. The environmental impact of glyphosate overuse has been reviewed in an article published by Organic Consumers Association.
In August of 2009 French researchers reviewed the evidence showing how glyphosates disrupt human reproductive hormones (androgens and estrogens). Their data indicates that glyphosate-based herbicides residues in food, feed, and the environment should be considered and classified as carcinogens and reproductive toxins – not unlike the PCBs of years gone by. Once again Monsanto sits in the middle of the controversy with human health hanging in the balance.
Does anyone trust Monsanto?
Avoid GMO food like the plague. Don’t buy any product made with GMO food or any product made by a company that uses any GMO food. Demand that GMO food be labeled so that consumers have a clear choice. And look out for sugar, the latest food to undergo Frankenfood mutation.
The FDA’s Peramivir H1N1 Swine Flu Experiment
The FDA has now opened the door for widespread human experimentation during this year’s flu season, allowing an antiviral drug called Peramivir to be used even though it has not passed traditional standards of safety testing. Ever since the FDA crafted its Critical Path agenda it has been looking for excuses to expose vulnerable Americans to toxic drugs under the false pretense of the greater good for all. The H1N1 Swine Flu fear-mongering is providing the cover that the FDA needs to unleash an experiment. The new Obama FDA administration has accepted the baton pass from the recently departed Bush FDA management team (von Eschenbach, et al.).
Hypocrisy at the FDA runs deep in their culture. The organization fails to warn the public of the known immunosuppressive effects of commonly used drugs such as antacids and statins – drugs that have been shown to increase the risk for infection. At the same time, the FDA has branded all nutrition as fraud. What right does the FDA have to brand nutrition as fraud? Nutrition has been battling influenza since humans have been around. Without nutrition humans would have never survived any flu pandemic. Nutrition is harmless to human health and invaluable to survival. In the FDA’s mind it is illegal. Rather, human experimentation is now deemed legal by the FDA. It’s all about protecting and expanding the profits of Big Pharma and Big Biotech.
Like Tamiflu and Relenza, Peramivir is a neuraminidase inhibitor. Neuraminidase (the N part of H1N1) is a viral protein that must be active in order for new viruses to emerge from a virally infected cell. If it can be blocked, then viral spreading can be reduced.
Tamiflu and Relenza only bind to neuraminidase for a brief period of time, limiting their biological activity against a virus. In contrast, Peramivir binds very tightly to neuraminidase and is longer lasting – meaning it is a much more potent drug. The FDA has approved it for use in advanced Swine Flu cases that are not responding to Tamiflu or Relenza.
On the one hand, this sounds like a reasonable approach to helping people with extreme Swine Flu. What is likely to happen in actual practice is another matter entirely. Doctors will hear on the grapevine how well Peramivir seems to work and it will be used on more and more patients. And what’s wrong with that?
It is a human experiment. Human experiments are against the Nuremberg code, which has been agreed to by the world following the atrocities of Nazi Germany. Human experiments run counter to the basic decency and morality of any culture – except the culture of the FDA and its profit-driven pharmaceutical allies.
The problem with neuraminidase blocking is that there are four known human genes that utilize neuraminidase for normal and healthy cell function (NEU1, NEU2, NEU3, NEU4). The next problem is that these genes are not passive and secondary in cellular function. They regulate carbohydrate-related communication taking place on human cell membranes (glyconutrition and glycobiology). In other words, they are instrumentally involved in how cells talk to each other, as well as in many processes of a cell’s internal communication. Any neuraminidase blocking drug runs the risk of interfering with general communication needed for healthy cell function.
The adverse side effects of Tamiflu are in many cases rather extreme and include panic attacks, delusions, delirium, convulsions, depression, loss of consciousness, and even suicide. Oxford researchers have publicly warned that Tamiflu is not for children. Tamiflu is a relatively weak binder of neuraminidase.
What is going to happen when a strong binder of neuraminidase, Peramivir, latches on to the human cellular communication system based on neuraminidase genes? The FDA has no idea, but their unelected bureaucratic management team has decided in their infinite wisdom that the benefits outweigh the risks, even though they have no way of knowing. The era of sanctioned human experimentation is upon us.
What if there was a substance that blocked neuraminidase regarding viral activity and left human neuraminidase alone? Wow, what a breakthrough that would be. Welcome to the world of nutrition. The real fraud can be found in the management team of the FDA.
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