World Health Organization sees ‘weak evidence’ of human poisoning by endocrine disruptors in chemicals

While admitting humans are experiencing the highest incidence of disease and that thousands of dangerous chemicals are used in products people consume, a World Health Organization report says there is only weak evidence that human health has been adversely affected by the abundance of those chemicals in food and other products.

By LUIS MIRANDA | THE REAL AGENDA | FEBRUARY 25, 2013

There are two facts that are undeniable when it comes to human health. First, despite great advances in science and technology, humans are sicker beings today –both mentally and physically–, when compared to half a century ago, for example. Even worse, the incidence of previously unknown or inexistant diseases has grown exponentially due to ‘inexplicable’ reasons. Second, those who were charged with verifying the safety of the production processes and the goods that are mass-produced for human consumption, failed to point out the dangers, and the side effects of thousands of substances used in the manufacture of industrial products.

The reason for the failure to properly guard human health and the environment from toxic chemicals varies, and it needs to be investigated on a case to case basis, but generally it occurred either due to lack of knowledge or because those watching out for our safety overlooked clear evidence that certain chemicals posed a direct threat to humanity and the environment. Three cases in point: DDT, fluoride in the water, mercury in vaccines, pesticides and herbicides.

In 2013, 41 years after its creation, the World Health Organization finally decided to publish a document where it expresses its concern about the adverse effects that toxic chemicals may have in humans; specifically on the human endocrine system. The document issued by the WHO titled Global Assessment of the State‐of‐the‐Science of Endocrine Disruptors, addresses what millions of people around the world, and thousands of health care practitioners have warned about for many years: chemicals put in the foods we eat, the water we drink and others used in industrial processes harm human health and gravely contaminate the environment.

Unfortunately, the report starts by playing down the role of industrial chemicals in the exponential appearance of disease among humans. The WHO cites as its final conclusion that “although it is clear that certain environmental chemicals can interfere with normal hormonal processes, there is weak evidence that human health has been adversely affected by exposure to endocrine-active chemicals.” As many other unaccountable global organizations, the WHO refused to look at independently gathered evidence that raised concerns about the poisoning of humans and the environment by the industrial process and how chemicals used in the production of food, for example, was the origin of previously unknown diseases.

It took 16 years for the WHO to accept and implement the advice provided by various health groups about the serious problem with the way food is produced as well as the way toxic chemicals are used in the production of the food we ingest. Back in 1997, the Intergovernmental Forum on Chemical Safety and the Environment Leaders of the Eight regarding the issue of EDCs, the International Programme on Chemical Safety (IPCS), a joint programme of WHO, UNEP and the International Labour Organization, began preparing the report issued in 2013.

Along with its general conclusion that its panel of scientists did not find enough evidence –despite all the evidence that exists– that human health is indeed adversely affected by exposure to endocrine disruptors found in toxic chemicals, the WHO report highlights just over a dozen other warning signs that humans, animals and the environment as a whole MAY be experiencing the consequences of systematic poisoning.

After explaining that life on Earth depends on its ability to reproduce and developed normally, the WHO report explains that there is a high incidence and a growing trend of endocrine-related disorders in humans; that there are observations of endocrine-related effects in wildlife populations; and that there is enough evidence that chemicals to which everyone is exposed to have endocrine disrupting properties linked to disease outcomes in laboratory studies. Amazingly, the WHO admits that there is more evidence to suggest that toxic chemicals DO cause endocrine disruptions on animals than on humans.

Endocrine Disruption

Figure 2. Overview of the endocrine system. Obtained from WHO report “State of the Science of Endocrine Disrupting Chemicals”. 2013.

The report found that endocrine-related diseases and disorders are on the rise, especially on young men. It related that in some countries, up to 40% of young men show low semen quality, which translates in their inability to have children. In addition to infertility, the report calls attention to the incidence of genital malformations, adverse pregnancy outcomes, neurobehavioural disorders associated with thyroid disruption, an unexplained rise in endocrine-related cancers that include breast, endometrial, ovarian, prostate, testicular and thyroid, earlier development of the breasts in young girls and the prevalence of obesity and type 2 diabetes, which increased exponentially all over the world for the past 40 years.

The World Health Organization reports that some 800 chemicals are confirmed or suspected to interfere with hormone receptors, hormonal synthesis or conversion and that only a small amount of those chemicals have been properly studied to determine their negative effects on the organisms. That is to say, health watchdogs –both at the national and international levels– traditionally failed to test for the potential or demonstrated threats that toxic chemicals used in the manufacture of food products presented to humans and other forms of life. “The vast majority of chemicals in current commercial use have not been tested at all,” the study admits.

As many independent observations have previously warned, humans and all life on this planet are continuously exposed to Endocrine Disruptive Chemicals (EDC), which traditionally occurs in low but permanent levels. The WHO report confirms this fact by saying that evidence shows that humans and wildlife are exposed to more EDCs than just those found in persistent organic pollutants. The report also confirms that food and drinking water are two major contributors of human and animal poisoning, but that the list of those elements that poison us all is long.

“Children can have higher exposures to chemicals compared with adults—for example, through their hand-to-mouth activity and higher metabolic rate. The speed with which the increases in disease incidence have occurred in recent decades rules out genetic factors as the sole plausible explanation.”

Endocrine Disruption in Babies

Figure 3. Sensitive windows of development. Each tissue has a specific window during development when it is forming. Obtained from WHO report “State of the Science of Endocrine Disrupting Chemicals”. 2013.

The statement above is damning evidence that most, if not all supposedly genetically transmitted diseases, are not really passed on to humans by their progenitors, but by their exposure to chemicals created or used during the production of food and other products. The report goes on detailing that chemicals such as DDT, PCB’s, diethylstilbestrol (DES) and polybrominated diphenyl ethers (PBDEs), often used in pesticides and herbicides, or for controlling insect reproduction, are to blame for breast cancer, prostate cancer, non-descended testes.

How can they then say that the evidence is weak when it comes to the relation between toxic chemicals and mass spread disease?

The assessment on endocrine disruptors clarified that much of the damage caused by toxic chemicals happens during pregnancy or early in human life. “Numerous laboratory studies support the idea that chemical exposures contribute to endocrine disorders in humans and wildlife.”

Again, where is the weak link then?

“Developmental exposures can cause changes that, while not evident as birth defects, can induce permanent changes that lead to increased incidence of diseases throughout life.

These insights from endocrine disruptor research in animals have an impact on current practice in toxicological testing and screening. Instead of solely studying effects of exposures in adulthood, the effects of exposures during sensitive windows in fetal development, perinatal life, childhood and puberty require careful scrutiny.”

The WHO report openly admits that organizations that are supposed to be vigilant about the adverse effects of poisons used in the industrial manufacture process have failed time after time to do that very task. “There has been a failure to adequately address the underlying environmental causes of trends in endocrine diseases and disorders.”

Is there room here for liability?

According to the WHO, disease risk induced by endocrine disrupting chemicals may have been significantly underestimated. That is to say, doctors and other health care practitioners who up until today follow the teachings of modern medicine as their base to diagnose disease while ignoring –sometimes purposely– the evidence presented by many studies on the adverse effects of EDC’s, are also to blame for current wave of ‘unknown’ or ‘untreatable disorders.

“We know that humans and wildlife are simultaneously exposed to many EDCs; thus, the measurement of the linkage between exposure to  mixtures of EDCs and disease or dysfunction is more physiologically relevant. In addition, it is likely that exposure to a single EDC may cause disease syndromes or multiple diseases, an area that has not been adequately studied.” Why not? Certainly nor because of lack of funding. Perhaps disinterest from the part of large pharmaceutical conglomerates who conduct their own studies with the ONLY intention to show whether a product is effective, but not to determine its safety or the long-term adverse effects on humans. The same is true for companies like Monsanto, DuPont, Syngenta and others which brag about their technological discoveries even though many independent tests prove, beyond reasonable doubt that their GMO’s, herbicides and pesticides are killing people all over the world.

Despite the mounting evidence presented in its own study, the skyrocketing incidence of disease in the last 50 years and the growing trends that show how EDC’s are more and more involved in causing adverse effects on human populations, the WHO again limits the relation between EDC’s and disease as a matter of association, instead of going beyond and calling it a matter of cause and effect. The report says that human studies can show associations only. But what happens when those associations continue to appear, study after study? Doesn’t that build a clear relationship of cause and effect?

Since most main stream corporate or government financed studies do not properly test for the effects of EDC’s on humans, because they are conducted with a very low number of subjects and for a very short time, the WHO has determined that this ‘association’ does not go beyond casual results that do not offer enough evidence to pose a cause and effect relationship. This is so, because although the mounting evidence, most tests are not designed to show that cause-effect relationship, which immediately invalidates them as reliable proof or evidence that toxic chemicals have –for a long time– caused disease in people and polluted the environment.

The report correctly points out that the shift already taking place from determining associations to testing for links –cause and effect– is the way to go to show what it deems as solid evidence that toxic chemicals indeed cause disease. But the WHO still fails to recognize what many studies have determined: that the adverse effects of early and continuous exposure to toxic chemicals are only detected late in life. Those effects, as explained before, are usually misdiagnosed by most doctors, who usually tell their patients that the origin of their illness is still unknown and that there is no way to treat the causes; only the symptoms. At this point, patients are condemned to taking pharmaceutical drugs for the rest of their lives, which eventually end up killing them due to their own adverse effects.

So, the state of human health today is equally bad from two different fronts. People are either killed by long-term exposure to toxic chemicals used in the production process of food or in the food itself, or they die while trying to ‘cure’ their diseases with industrialized pharmaceuticals whose own side effects are as deadly as those from the chemicals people are trying to get rid of. Either way, people die long, painful deaths.

So what is next? What needs to be done to end this vicious circle of disease? Can long-term studies be the solution? I think it is too little too late for that. Waiting another 10 or 20 years to see the result of long-term tests is not something a lot of people can afford now. That does not mean that those studies should not be done. It means that people need to find solutions by themselves. Now that the World Health Organization has finally confessed they have not done their job to protect people from dangerous substances –quite the opposite is true–  people need to understand that their nutrition is their responsibility. It always has been so. From the part of the organizations that are supposed to keep us safe from the dangers of toxic chemicals, it is time to stop talking and start walking.

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Radiation creates Cancer Cells 30 Times More Potent than Regular Cancer Cells

By TONY ISAACS | NATURAL NEWS.COM | MARCH 19, 2012

In a groundbreaking new study just published in the peer reviewed journal Stem Cells, researchers at UCLA’s Johnsson Comprehensive Cancer Center Department of Oncology found that, despite killing half of all tumor cells per treatment, radiation treatments on breast cancer transforms other cancer cells into cancer stem cells which are vastly more treatment-resistant than normal cancer cells. The new study is yet another blow to the failed and favored mainstream treatment paradigm of trying to cut out, poison out or burn out cancer symptoms (tumors) instead of actually curing cancer.

Senior study author Dr. Frank Pajonk, associate professor of radiation oncology at the Jonsson Center, reported that induced breast cancer stem cells (iBCSC) “were generated by radiation-induced activation of the same cellular pathways used to reprogram normal cells into induced pluripotent stem cells (iPS) in regenerative medicine.” Pjonk, who is also a scientist with the Eli and Edythe Broad Center of Regenerative Medicine at UCLA, added “It was remarkable that these breast cancers used the same reprogramming pathways to fight back against the radiation treatment.”

In the new study, Pajonk and his team irradiated normal non-stem cell cancer cells and placed them into mice. Through a unique imaging system, the researchers observed the cells differentiate into iBCSC in response to radiation treatments. Pjonk reported that the newly generated cells were remarkably similar to non-irradiated breast cancer stem cells. The team of researchers also found that the radiation-induced stem cells had a more than 30-fold increased ability to form tumors compared with non-irradiated breast cancer cells.

Despite mounting evidence, mainstream medicine clings to surgery, chemo and radiation and ignores natural solutions

Despite all the billions of dollars spent on cancer, the 40 year “war on cancer” has been a losing one by any honest evaluation. One hundred years ago, anywhere from 1 in 50 to perhaps 1 in 100 people could be expected to develop cancer. Now it is estimated that 1 in every 2 men and 1 in every 3 women will be diagnosed with cancer in their lifetimes. Despite more people around the world developing cancer and dying from cancer every year, mainstream medicine continues to cling to failed treatments which more often than not fail to eliminate the cancer and help cancer spread and return more aggressively than ever. Notably, two of the three major mainstream cancer treatments – radiation and chemo – are themselves highly carcinogenic.

One might think that the new study provided ample reasons to rethink using radiation. However, the study authors looked at the results as an opportunity to continue and enhance the use of radiation by finding ways to control the cell differentiation. What the scientists failed to note is that natural alternatives have already been found which prevent the development of cancer stem cells.

As just one example, Natural News reported in May 2010 that a University of Michigan study had found a compound in broccoli and broccoli sprouts which had the ability to target cancer stem cells. See:
http://www.naturalnews.com/028822_broccoli_breast_cancer.html

The researchers failed to note how cancer cells fought against unnatural treatments. They also failed to take into account the mounting evidence that the best way to beat cancer as well as avoid it is to build and enhance our natural first line of defense – our immune system.

The safest and most effective way to enhance the natural immune system and fight cancer in general is by working with nature. It is also by far the least expensive way, and therein likely lies the rub. You can’t patent and profit from nature like you can with mainstream drugs and treatments.

Note: Neither NaturalNews nor this author condone the inhumane use of animals in medical studies.

Other sources included:

www.cancer.ucla.edu/Index.aspx?page=644
www.sciencedaily.com/releases/2012/02/120213185115.htm
www.naturalnews.com/cancer_cells.html
www.naturalnews.com/stem_cells.html

Sleep Deprived? Avoid Using Nuvigil

Pricey Nuvigil competes with coffee—and has a lot more side effects. Nuvigil “may lead to limited physical or psychological dependence…” Cephalon also reports plenty of side effects ranging from headache, nausea, skin rashes, hallucinations and depression.

By
Bloomberg
August 14, 2011

Roger Greer, a 45-year-old water treatment plant worker from Coatesville, Pa., was surfing the Internet when he discovered that his constant fatigue had a medical name: shift work sleep disorder. The starting time of Greer’s job rotates weekly, leaving him sleepy on the job and ornery at home. The website had an ad suggesting he ask his doctor if an alertness pill made by Cephalon (CEPH), called Nuvigil, is right for him. A year later, “I don’t have those sleepy moments,” says Greer. “Now at 3 in the morning, the absolute worst time for anybody, I no longer have the fear of missing something here at work.”

Workers like Greer are prime targets for a Cephalon marketing campaign—on the Internet and radio, in doctors’ offices, and at community meetings—that aims to educate America’s 15 million shift workers about the disorder. For the drug maker, it’s a way to build brand recognition and sales for Nuvigil, a newer version of its blockbuster narcolepsy drug, Provigil, which loses patent protection next year. But the campaign has sparked concern by some doctors about whether a pharmaceutical solution is the best way to stay alert on the job. Nuvigil hasn’t been proved more effective than coffee, is classified as possibly addictive, and carries side effects that can be fatal, according to the drug’s label.

“We as a society rely too much on pills and medication,” says Robert Basner, director of Columbia University’s Cardiopulmonary Sleep and Ventilatory Disorders Center. “That’s not always the best approach. Caffeine is a very good wake-promoting agent, and it’s a lot cheaper.”

Cephalon is spending $3.6 million on radio ads pitching Nuvigil, plus about $490,000 annually on the Internet effort and informational booths at community events. That’s a small percentage of the $1.1 billion in annual sales that will be at risk after Provigil goes off-patent. Israel’s Teva Pharmaceutical Industries (TEVA) agreed in May to buy Cephalon for $6.2 billion in part because of Nuvigil’s prospects. The drug’s sales are growing at a 50 percent annual rate.

Bethany Young, a 27-year-old Teas Valley (W. Va.) medical technologist, was given free samples of Nuvigil after complaining to her new doctor that she couldn’t focus during her 7 p.m. to 7 a.m. hospital shifts. During six years of night work, she struggled to get out of bed, gained 60 pounds, and developed hypothyroidism. At first the drug made her feel euphoric. Soon that effect began to melt away after an hour, replaced by feelings of anxiety and stress, she says, and when she tried to stop using it after a few months, she initially couldn’t. “I was getting hooked on it. I couldn’t quit. This drug is the devil. It was for me, anyway.”

Cephalon says that because medications like Nuvigil “may lead to limited physical or psychological dependence, we encourage physicians to follow patients closely.” The company also reports plenty of side effects that can accompany Nuvigil use, ranging from headache, nausea, and skin rashes to hallucinations and depression.

Cephalon’s media campaign is its first to widely trumpet alertness pills by stressing the recognition of shift work disorder by doctors and sleep experts, who estimate the malady may affect one in four shift workers. Although Cephalon doesn’t claim Nuvigil works better than other approaches, the company says that between 2007 and 2009 it studied 359 shift workers for six weeks and found 77 percent of those who took Nuvigil said they were more alert for the last part of their shift and the drive home, compared with 57 percent given a placebo.

“What we are doing is educating doctors and the public about this disorder,” says Charles Altman, Cephalon’s senior medical director. “Doctors often don’t ask patients what hours they work. In our 24/7 society, it doesn’t matter if you are a nurse or an information technology worker or in finance, we are called upon more and more to work odd hours that are against the grain of the way our internal clock works.”

Critics, however, say the diagnosis of shift work sleep disorder is so broad that people with irregular hours who have trouble staying awake at night can get the pills even without trying non-drug strategies first. “It’s not a diagnosis that is crisp and determined by clear-cut, objective data, which opens it up to criticism,” says Lois Krahn, chair of psychiatry at the Mayo Clinic in Scottsdale, Ariz. “When [patients] have done everything they can to get more sleep, and they still have trouble staying awake, that’s when drug therapy comes in.”

Besides the ad push, Cephalon is using pricing to lure users. At $12 a pill, Nuvigil sells for $5 less than its older sibling. Cephalon also is providing consumers with coupons for free trials and help with insurance co-pays to spur use of the newer drug. The strategy is paying off, with the number of Nuvigil prescriptions written in late June almost equaling those for Provigil. “It’s growing very nicely,” says Cephlon’s Altman.

Provigil was first approved for sale in 1998 as a treatment for narcolepsy, a rare condition in which patients unexpectedly fall asleep in the middle of the day. Provigil kept them awake, without the dangers of stimulants. Sales, which surged as people without the condition also used it, topped $500 million annually after the pill won clearance for shift work disorder in 2004. Nuvigil was introduced in 2009, two years after it was approved for narcolepsy, shift work disorder, and sleep apnea. It had sales of $186 million in 2010, and analysts say it could hit $577 million in 2015.

Sleep experts say Cephalon’s radio ads in 21 big U.S. cities may educate patients with symptoms that employers and family members often don’t understand. Still, doctors say simply handing struggling shift workers a prescription would be a mistake without trying lifestyle changes, such as strategic naps or wearing sunglasses on the drive home to limit exposure to light. Explains Douglas Moul, staff physician at the Cleveland Clinic Sleep Center: “We want to treat the real condition, rather than just papering over the symptoms with a medication that can just keep people awake longer.”

The bottom line: Sales of Cephalon’s shift work disorder drug, Nuvigil, are growing 50 percent annually. Critics say the pills may be overprescribed.

Medicinal Herbs to be Illegal in European Union

Heidi Stevenson

Big Pharma has almost reached the finish line of its decades-long battle to wipe out all competition. As of 1 April 2011—less than eight months from now—virtually all medicinal herbs will become illegal in the European Union. The approach in the United States is a bit different, but it’s having the same devastating effect. The people have become nothing more than sinks for whatever swill Big Pharma and Agribusiness choose to send our way, and we have no option but to pay whatever rates they want.

Big Pharma and Agribusiness have almost completed their march to take over every aspect of health, from the food we eat to the way we care for ourselves when we’re ill. Have no doubt about it: this takeover will steal what health remains to us.

It Begins Next April Fools Day

In the nastiest April Fool’s Joke of all time, the European Directive on Traditional Herbal Medicinal Products (THMPD) was enacted back on 31 March 2004.(1) It laid down rules and regulations for the use of herbal products that had previously been freely traded.

This directive requires that all herbal preparations must be put through the same kind of procedure as pharmaceuticals. It makes no difference whether a herb has been in common use for thousands of years. The costs for this are far higher than most manufacturers, other than Big Pharma, can bear, with estimates ranging from £80,000 to £120,000 per herb, and with each herb of a compound having to be treated separately.

It matters not that a herb has been used safely and effectively for thousands of years. It will be treated as if it were a drug. Of course, herbs are far from that. They’re preparations made from biological sources. They aren’t necessarily purified, as that can change their nature and efficacy, just as it can in food. It’s a distortion of their nature and the nature of herbalism to treat them like drugs. That, of course, makes no difference in the Big Pharma-ruled edifice of the EU, which has enshrined corporatism in its constitution.

Dr. Robert Verkerk of the Alliance for Natural Health, International (ANH) describes the problem of requiring drug-like compliance on herbal preparations:

Getting a classical herbal medicine from a non-European traditional medicinal culture through the EU registration scheme is akin to putting a square peg into a round hole. The regulatory regime ignores and thus has not been adapted to the specific traditions. Such adaptation is required urgently if the directive is not to discriminate against non-European cultures and consequently violate human rights.(2)

Trade Law

To best understand how this can be happening, one needs to see that trade laws have been at the center of the moves to place all aspects of food and medicine under the control of Big Pharma and Agribusiness.

If you’ve followed what’s been happening in the United States regarding raw milk and the Food and Drug Administration’s (FDA’s) claims that foods magically become drugs when health claims are made, you may have noted that the Federal Trade Commission (FTC) has been part of the process.

Rather than treating food and traditional medicines as human rights issues, they have been treated as trade issues. That makes the desires of large corporations the focus of food and herbal law, rather than the needs and desires of people. It’s this twisting that has resulted in the FDA’s making outrageously absurd statements, such as claiming that Cheerios and walnuts quite literally become drugs simply because of health claims made for them.

The goal of it all is to make the world safe for the megacorporations to trade freely. The needs and health of the people simply are not a factor in their considerations.

How to Fight This Encroachment on Our Health and Welfare

It’s not a done-deal, at least, not quite. If you value your access to herbs, or if you care about access to vitamins and other supplements, please take action. Even if these issues seem meaningless to you, consider the people who do care. Should they be denied the right to the medical treatment and health maintenance of their choice?

The ANH has been active in fighting these encroachments. They are currently going to court in an attempt to stop the implementation of THMPD. We can hope that they’ll succeed, but recent history shows that no legal maneuver is likely to stop this juggernaut. We cannot afford to sit back and wait for the results of their efforts. We need to see their endeavor as part of a whole, one in which each of us plays a role.

It’s up to us—each and every one of us—to take action. If you live in Europe, please, send a letter or message to your Member of European Parliament. Go to this page to find out who is your MEP and the contact information. Then, send a letter that states, in no uncertain terms, that you strongly support the ANH’s actions in trying to suspend the implementation of THMPD and that you hope they will also take a stand in support of the people’s right to choose herbal treatments.

If you find it difficult to write such a letter, click here for a sample (in the universal .rtf format) suggested by ANH. Feel free to use it.

Try to imagine facing your children or grandchildren when they ask why you didn’t. How will you tell them that you really weren’t that interested in their welfare? How will you tell them that it was more important to watch the latest fake reality show on television than to take the time to write a simple letter?

It is only by actively protesting that this travesty against our welfare can be stopped. If we sit back in apathy, then it will happen. Our right to protect our health and that of our children is hanging in the balance. If you care for your child’s or grandchild’s welfare, then you must act. Speak out, for now is the moment of truth. You can sit back and do nothing, or you can speak out.

And then, once you have, talk to everyone you know. Tell them that it’s time to act. There truly is no time to waste.

Choosing healthy foods now called a mental disorder

NaturalNews.com

In its never-ending attempt to fabricate “mental disorders” out of every human activity, the psychiatric industry is now pushing the

Eating healthy foods, pseudo-scientists say, is sign of a mental disorder.

most ridiculous disease they’ve invented yet: Healthy eating disorder.

This is no joke: If you focus on eating healthy foods, you’re “mentally diseased” and probably need some sort of chemical treatment involving powerful psychotropic drugs. The Guardiannewspaper reports, “Fixation with healthy eating can be sign of serious psychological disorder” and goes on to claim this “disease” is called orthorexia nervosa — which is basically just Latin for “nervous about correct eating.”

But they can’t just called it “nervous healthy eating disorder” because that doesn’t sound like they know what they’re talking about. So they translate it into Latin where it sounds smart (even though it isn’t). That’s where most disease names come from: Doctors just describe the symptoms they see with a name like osteoporosis (which means “bones with holes in them”).

Getting back to this fabricated “orthorexia” disease, the Guardian goes on to report, “Orthorexics commonly have rigid rules around eating. Refusing to touch sugar, salt, caffeine, alcohol, wheat, gluten, yeast, soya, corn and dairy foods is just the start of their diet restrictions. Any foods that have come into contact with pesticides, herbicides or contain artificial additives are also out.”

Wait a second. So attempting to avoid chemicals, dairy, soy and sugar now makes you a mental health patient? Yep. According to these experts. If you actually take special care to avoid pesticides, herbicides and genetically modified ingredients like soy and sugar, there’s something wrong with you.

But did you notice that eating junk food is assumed to be “normal?” If you eat processed junk foods laced with synthetic chemicals, that’s okay with them. The mental patients are the ones who choose organic, natural foods, apparently.

What is “normal” when it comes to foods?

I told you this was coming. Years ago, I warned NaturalNews readers that an attempt might soon be under way to outlaw broccoli because of its anti-cancer phytonutrients. This mental health assault on health-conscious consumers is part of that agenda. It’s an effort to marginalize healthy eaters by declaring them to be mentally unstable and therefore justify carting them off to mental institutions where they will be injected with psychiatric drugs and fed institutional food that’s all processed, dead and full of toxic chemicals.

The Guardian even goes to the ridiculous extreme of saying, “The obsession about which foods are “good” and which are “bad” means orthorexics can end up malnourished.”

Follow the non-logic on this, if you can: Eating “good” foods will cause malnutrition! Eating bad foods, I suppose, is assumed to provide all the nutrients you need. That’s about as crazy a statement on nutrition as I’ve ever read. No wonder people are so diseased today: The mainstream media is telling them that eating health food is a mental disorder that will cause malnutrition!
Shut up and swallow your Soylent Green

It’s just like I reported years ago: You’re not supposed to question your food, folks. Sit down, shut up, dig in and chow down. Stop thinking about what you’re eating and just do what you’re told by the mainstream media and its processed food advertisers. Questioning the health properties of your junk food is a mental disorder, didn’t you know? And if you “obsess” over foods (by doing such things as reading the ingredients labels, for example), then you’re weird. Maybe even sick.

That’s the message they’re broadcasting now. Junk food eaters are “normal” and “sane” and “nourished.” But health food eaters are diseased, abnormal and malnourished.

But why, you ask, would they attack healthy eaters? People like Dr. Gabriel Cousens can tell you why: Because increased mental and spiritual awareness is only possible while on a diet of living, natural foods.

Eating junk foods keeps you dumbed down and easy to control, you see. It literally messes with your mind, numbing your senses with MSG, aspartame and yeast extract. People who subsist on junk foods are docile and quickly lose the ability to think for themselves. They go along with whatever they’re told by the TV or those in apparent positions of authority, never questioning their actions or what’s really happening in the world around them.

In contrast to that, people who eat health-enhancing natural foods — with all the medicinal nutrients still intact — begin to awaken their minds and spirits. Over time, they begin to question the reality around them and they pursue more enlightened explorations of topics like community, nature, ethics, philosophy and the big picture of things that are happening in the world. They become “aware” and can start to see the very fabric of the Matrix, so to speak.

This, of course, is a huge danger to those who run our consumption-based society because consumption depends on ignorance combined with suggestibility. For people to keep blindly buying foods, medicines, health insurance and consumer goods, they need to have their higher brain functions switched off. Processed junk foods laced with toxic chemicals just happens to achieve that rather nicely. Why do you think dead, processed foods remain the default meals in public schools, hospitals and prisons? It’s because dead foods turn off higher levels of awareness and keep people focused on whatever distractions you can feed their brains: Television, violence, fear, sports, sex and so on.

But living as a zombie is, in one way quite “normal” in society today because so many people are doing it. But that doesn’t make it normal in my book: The real “normal” is an empowered, healthy, awakened person nourished with living foods and operating as a sovereign citizen in a free world. Eating living foods is like taking the red pill because over time it opens up a whole new perspective on the fabric of reality. It sets you free to think for yourself.

But eating processed junk foods is like taking the blue pill because it keeps you trapped in a fabricated reality where your life experiences are fabricated by consumer product companies who hijack your senses with designer chemicals (like MSG) that fool your brain into thinking you’re eating real food.

If you want to be alive, aware and in control of your own life, eat more healthy living foods. But don’t expect to be popular with mainstream mental health “experts” or dietitians — they’re all being programmed to consider you to be “crazy” because you don’t follow their mainstream diets of dead foods laced with synthetic chemicals.

But you and I know the truth here: We are the normal ones. The junk food eaters are the real mental patients, and the only way to wake them up to the real world is to start feeding them living foods.

Some people are ready to take the red pill, and others aren’t. All you can do is show them the door. They must open it themselves.

In the mean time, try to avoid the mental health agents who are trying to label you as having a mental disorder just because you pay attention to what you put in your body. There’s nothing wrong with avoiding sugar, soy, MSG, aspartame, HFCS and other toxic chemicals in the food supply. In fact, your very life depends on it.

Oh, and by the way, if you want to join the health experts who keep inventing new fictitious diseases and disorders, check out my popular Disease Mongering Engine web page where you can invent your own new diseases at the click of a button! You’ll find it at:http://www.naturalnews.com/disease-…