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Information Liberation - by TruthSeeker

By Richard A. Warner
Online Journal Contributing Writer

Nov 29, 2006, 01:17

Under the guise of combating the stigma of mental illness, the U.S. government will soon begin a massive campaign of psychiatric indoctrination, designed to increase the acceptance of psychiatric chemical imbalance theories and labeling, and to pave the way for national psychiatric screening, driving more Americans into seeking psychiatric drug treatment.

Regional meetings in support of the National Anti-Stigma Campaign (NASC), a nationwide television, radio and print public service advertising program funded by the Substance Abuse and Mental Health Services Administration (SAMHSA), were held this past summer in Los Angeles, Denver, Chicago and Washington, D.C. According to a senior technical assistance specialist at the SAMHSA Resource Center to Address Discrimination and Stigma Associated with Mental Illness (ADS Center), the ad campaign, which will target 18-25-year olds, will be launched today. A campaign directed at older adults and ethnic and racial minorities will follow.


On its surface, the campaign’s message may seem perfectly appropriate, even compassionate. Its stated objective is to “encourage, educate and inspire 18-25-year olds to step up and support friends they know are experiencing a mental health problem.” One ad, for example, shows a man with his hand over his eyes. “Sometimes I find myself turning away from or just ignoring someone with a mental illness, avoiding eye contact,” he says. “I know it is not their fault but sometimes I don’t know how to communicate with them.”

But there can be no doubt about the real purpose of the campaign’s emotional appeal: to create customers for the psychiatric/pharmaceutical industry. This is clearly evident at SAMHSA’s website and in its literature. It is no accident that 18-25-year olds were chosen as the first target. A SAMHSA “Fact Sheet” states, “Among 18-25-year olds, the prevalence of serious mental health conditions is high . . . yet this age group shows the lowest rate of help-seeking behaviors [emphasis added].” “Help-seeking behavior” is, of course, a euphemism for being psychiatrically diagnosed and drugged. The 18-25-year old demographic represents a huge untapped market for psychiatric drugs and services. According to SAMHSA’s website, the anti-stigma media blitz “has been designed to establish a ‘new norm,’ in which individuals, without hesitation, will seek out the mental health services they need and deserve.”


The drug industry seeds NASC

Further evidence of SAMHSA’s marketing agenda is found in the origins of the National Anti-Stigma Campaign. The program was first recommended by a federal commission that had extensive ties to the pharmaceutical industry. In its 2003 report, Achieving the Promise: Transforming Mental Health Care in America, the President’s New Freedom Commission (NFC) on Mental Health called for the government to “undertake a national campaign to reduce stigma.” The NFC proposed “national education initiatives” to “shatter the misconceptions about mental illnesses, thus helping more Americans understand the facts and making them more willing to seek help for mental health problems” and advocated “actions of reducing stigma, increasing awareness, and encouraging treatment . . . (emphasis added).”

Several members of the NFC had extensive ties to the pharmaceutical industry, principally by way of an industry marketing scheme that was developed in Texas in the 1990s. Known as the Texas Medication Algorithm Project, or TMAP, it was designed to make the newest and most expensive psychiatric drugs the first (and virtually only) treatment option for mental health care. The project was nurtured at the University of Texas Southwestern Medical Center in Dallas, a major research center that conducts drug trials for pharmaceutical companies, with significant funding coming from the drug companies themselves. Pharmaceutical company gifts to the Texas Department of State Health Services totaled $1.3 million from 1997 to 2004, with at least $834,000 earmarked for TMAP.

Backed by drug industry funding, TMAP was then exported to other states via the National Association of State Mental Health Program Directors (NASMHPD).

The chair of the NFC, Michael Hogan, was the Mental Health Program Director in Ohio when the Ohio Medication Algorithm Project (OMAP), was adopted there. A 2004 Janssen (makers of the atypical antispsychotic, Risperdal) publication, “Mental Health Issues Today,” lists Hogan as a member of their Advisory Board. In 2005, Eli Lilly (makers of the atypical antipsychotic, Zyprexa and the antidepressant, Prozac) gave Hogan its Lifetime Achievement Award. Hogan was president of the NASMHPD from 2003-2004 and president of the NASMHPD Research Institute, which is heavily funded by the pharmaceutical industry, from 1989-2000.

Another NFC member, Stephen Mayberg, was the California State Mental Health Program Director when TMAP was adopted in that state. Mayberg is also a past president of NASMHPD and the NASMHPD Research Institute.

NFC member Charles Curie, who recently stepped down as the administrator of SAMHSA, was the Deputy Secretary for Mental Health and Substance Abuse Services in Pennsylvania when PENNMAP was enacted. According Allen Jones, an investigator in the Pennsylvania Office of Inspector General and a whistleblower, Curie is reported to have set up a slush fund from which state employees could solicit grants from the pharmaceutical industry.

NFC member psychiatrist Rodolfo Arredondo served on the board of the Texas Department of Mental Health and Mental Retardation during TMAP’s development, while another NFC commissioner, Robert Postlethwait, has had a long career with Eli Lilly and Company.

According to Jones, at least 14 of the 22 NFC members have drug industry ties. Not surprisingly, the NFC selected TMAP as a model program and stated that the “biggest challenge” was to ensure that TMAP was “implemented in other states and localities.”

The psychiatric industry is well on its way to meeting that challenge -- with disastrous results for our youth. A similar pattern emerges in states which have adopted TMAP. In Texas, 19,404 teenagers were prescribed an antipsychotic in July or August of 2004. Ninety-eight percent received the newer atypical antipsychotics. In April of 2004, the Texas Comptroller, Carole Strayhorn, released a report, Forgotten Children, that was highly critical of the psychiatric drugging of foster children in Texas.

In 2005, the Columbus (Ohio) Dispatch ran a two-part story, “Drugged Into Submission,” on the psychiatric drugging of children, including 700 babies and toddlers, under state care. Part one was titled, “Forced Medication Straitjackets Kids.”

In 1998, the Los Angeles Times reported, “Children under state protection in California group and foster homes are being drugged with potent, dangerous psychiatric medications, at times just to keep them obedient and docile for their overburdened caretakers.”

In Pennsylvania, Dr. Stephan Kruszewski, a Harvard trained psychiatrist working for the Pennsylvania’s Department of Public Welfare, complained that children were being heavily drugged with antipsychotics and anticonvulsants (mainly Neurontin). He was fired.

In Washington State, atypical antipsychotics ranked 1, 3, and 5 on the Medical Assistance Administration’s list of top 100 drugs by money paid in 2004, with nearly $78 million spent on those three drugs: Zyprexa ($36 million), Risperdal ($21 million), Seroquel ($20.8 million). Neurontin was #4, at $20.8 million. Antidepressants Zoloft, Effexor and Paxil came in at #7, #11 and #12, with nearly $31 million spent on those three drugs. A 1997 Seattle Post-Intelligencer series charged that an “unmonitored stream of mood drugs imperils children entrusted to state.”

Additional confirmation of the drug industry’s control of SAMHSA comes in the form of an email sent to me by the previously mentioned senior technical assistance specialist at SAMHSA. The email was a response to my inquiry about the anti-stigma campaign. The assistance specialist sent a copy of her response and my original inquiry, to the NASC liaison at NAMI. NAMI, of course, is the National Alliance for the Mentally Ill, a well-known front group for the pharmaceutical industry. SAMHSA is obviously working hand in hand with NAMI -- even forwarding private communication from the public to NAMI’s offices. In 1999, Mother Jones magazine reported that 18 drug firms gave NAMI a total of $11.72 million between 1996 and 1999. NAMI continually promotes psychiatric chemical imbalance theories, minimizes the damaging effects of psychiatric drugs, and advocates for forced psychiatric drugging programs.

On May 28, 2006, the Philadelphia Inquirer reported that NAMI “did not disclose that Lilly [Eli Lilly, makers of Zyprexa and Prozac] marketing manager Gerald Radke briefly ran its entire operation. Radke began in 1999 as a Lilly-paid ‘management consultant,’ then left Lilly and served as NAMI's paid ‘interim executive director’ until mid-2001. The group acknowledged this only after being shown Radke's resume listing the job.”

According to the Inquirer, Lilly gave NAMI $3 million between 2003 and 2005 and “called its executive loans mutually beneficial.” NAMI’s former executive director for 16 years was Laurie Flynn. Flynn is now the Director of Teenscreen, a psychiatric screening program developed by Columbia University’s Child Psychiatry Research Department and, not surprisingly, recommended by the NFC. TeenScreen’s goal is to screen all teenagers in the U.S. for psychiatric disorders.

NASC and screening: Educating Americans to be good customers

Since psychiatric drugging must, in most cases, be preceded by the assignment of a psychiatric label, psychiatric screening is an essential step in the industry’s plans to expand its market. That’s where the anti-stigma campaign and national psychiatric screening -- both recommended by the NFC -- come into play.

The NFC report recommended “early detection of mental health problems in children and adults -- through routine and comprehensive testing and screening . . ." and while NFC chair Hogan has denied that the NFC intended universal screening, in a January 20, 2005 story in the Christian Science Monitor, Hogan said that the commission decided that recommending universal screening would be "a little premature and probably controversial, even though we thought, in the long run, it probably might be the right thing to do.”

In other words, the only barrier to screening everyone in America, as the NFC sees it, is the controversy it would generate. It’s “premature.” Americans have to be prepared to accept mass psychiatric interventions. SAMHSA’s NFC-recommended NASC program is their answer -- a three-year, “long run” program to prepare the population for universal screening, followed, of course, by psychiatric labeling and drugging.

The NASC campaign will advertise that mental illness has reached epidemic levels in the population -- a theme that has been repeated in psychiatric marketing campaigns dating back to the 1940s. The psychiatric industry wants Americans to see mental illness everywhere -- to associate any problem in life with a possible psychiatric disorder that can be treated with a psychiatric drug.

A PowerPoint presentation available at the NASC website warns that “22% of Americans have a diagnosable mental health problem” but “the majority . . . do not seek help.” SAMHSA has produced three brochures that focus on the workplace (Mental Health: It’s Part of Our Lives at Work), the elderly (Mental Health: It’s Part of Aging) and college students (Mental Health: It’s Part of College Life). All state that one in five adults in the U.S. experience a mental illness each year. All stress that not enough people are seeking treatment due to stigma.

At the same time SAMHSA’s Eliminating Barriers Initiative (EBI) is currently being pushed into secondary schools via school administrators' associations. EBI is being piloted in eight states, (Mass., Ohio, Fla., NC, Calif., Texas, Wisc. Pa.). EBI training presentations promoting psychiatric chemical imbalance theories, stating, “Mental illnesses are brain disorders.”

In Massachusetts, the commissioner of Mental Health was brought to one conference and read a student’s suicide note to the assembled school administrators. Suicide is a favorite theme, even though 1) child suicides are extremely rare (4.6 per 100,000 in 2001, according to the Center for Disease Control) and declining; 2) In 2004, the U.S. Preventive Services Task Force (USPSTF) found “no evidence that screening for suicide risk reduces suicide attempts or mortality” and "insufficient evidence that treatment of those at high risk reduces suicide attempts or mortality;” and 3) psychiatric drug treatment has been found to increase suicidal thinking and behavior in children under 18.

The goal of such programs is clear. SAMHSA, acting as a tool of the psychiatric and drug industries, wants Americans to view the world through psychiatric lenses -- to find mental illness in their children, their colleagues, their family and friends. The purpose of the NASC campaign is not to educate Americans about psychiatric theories and treatments but to instill acceptance of psychiatric dogma and psychiatric labeling and thus prepare the way for psychiatric screening and drugging. Always the appeal is heavily weighted to the emotions. The elderly brochure, for example, advises, “If you feel shame because you have a mental illness remember: You are not alone.” SAMHSA will tell us that fear of the mentally ill is part of the stigma, while, at the same time, they will be sowing a subliminal fear that mental illness is lurking around every corner.

The NASC campaign will spread the gospel of chemical imbalances and suggest that the stigma of mental illness is the result of public ignorance and fear. This is a key element of NASC. Americans must be taught to locate the source of the stigma in their own personal failure, not the rampant disease mongering and fear tactics of the psychiatric industry.

The real source of the stigma

The real source of the stigma of mental illness lies in the definition of stigma itself. The dictionary says a stigma is “A mark or token of infamy, disgrace or reproach. A small mark; a scar or birthmark.” The word derives from the ancient word for the mark or tattoo that was carved or burned into the flesh of a slave or prisoner to inform everyone of their shameful status.

The definition of stigma suggests at once the source of the stigma -- psychiatric “marking” -- and how it could be eliminated: Don’t place the mark. The most direct way to end the stigmatization of the mentally ill would be to stop calling them mentally ill and labeling them with specious disorders. After all, there’s no proof they’re ill. There is no lab test that can verify the presence of any psychiatric disorder. We could just get rid of the Attention Deficits, the Major Depressives, the Social Anxieties, the Bipolars and the 370 other labels psychiatrists have invented to alienate and marginalize those who are suffering and convince those who are well that they are ill. We could tell the psychiatric prisoners that their diagnostic cells are a thin illusion, that their experience is part of the infinite variety of human experience. We could tell them they are not other than us, they are not sick, they don’t have bad brains. Life is tough, for a thousand different reasons, and most of us struggle.

If we just put an end to psychiatry’s fraudulent pathologizing of life, the stigma of mental illness would disappear.

Needless to say, this is not the kind of campaign SAMHSA has planned. There’s too much money at stake. For several decades now psychiatrists have been manufacturing stigmas at a ridiculous rate. Psychiatry’s book of stigmas, the Diagnostic and Statistical Manual of Mental Disorders, has expanded from 112 stigmas in 1952 to its current 374, under the guiding hand, the New York Times and others recently (April 20) reported, of “experts” with financial ties to drug companies.

According to the Times, a study in the journal Psychotherapy and Psychosomatics found that “56 percent of 170 experts who worked on the 1994 edition of the manual, called the Diagnostic and Statistical Manual, or D.S.M, had at least one monetary relationship with a drug maker in the years from 1989 to 2004.” A report on the study in the Chicago Tribune noted that, “100 percent of the experts on DSM-IV panels overseeing mood disorders and schizophrenia/psychotic disorders were financially involved with the drug industry. These are the largest categories of psychiatric drugs in the world, racking up 2004 sales of $20.3 billion and $14.4 billion, respectively. Depression is the leading mood disorder.”

It’s a particularly profitable symbiosis. Psychiatrists invent the diseases; the pharmaceutical industry makes the snake oil to treat them. And as we have seen, the purpose of the NASC campaign is to help the experts and drug companies cash in on their cozy relationship, to ensure that Americans accept psychiatric branding and become good customers for the psychiatric/pharmaceutical complex.

The last thing the psychiatric industry wants is for people to have the facts about psychiatry’s invented illnesses and ineffective, damaging drugs. SAMHSA’s campaign will follow a different script, one with more of a “slaves are people too” theme, one which ensures that psychiatric branding is broadly accepted.

A brochure from the ADS center asks that we “remember” that people with mental illnesses “do recover and lead productive lives,” they have the “same needs as everyone else,” they “make valuable contributions to society,” and discrimination “keeps them from seeking help” and “violates their rights.”

In other words, we will be educated about how people become slaves (mentally ill); that it’s not their fault (it’s genetic); that slavery touches all of us, and that, while slaves are different, they should be treated with dignity. Slaves can lead productive lives, they have the same needs as everyone, they make valuable contributions, and you shouldn’t discriminate against them. We’ll be told that psychiatric prisoners are fortunate to have kind wardens who treat them with respect and though the whip is occasionally needed, it’s all in their best interests. Just don’t start thinking that they are normal human beings -- they are slaves, i.e., mentally disordered with damaged brains.

SAMHSA’s campaign will justify and expand the stigmatization that supports the current mental health system, while chiding us to be nice to those who are thereby victimized. It won’t tell us how psychiatrists invent their diagnoses. It won’t tell that psychiatry’s own diagnostic manual admits that psychiatry can’t distinguish one disorder from another or mental illness from mental health. It won’t tell us that psychiatric diagnostic reliability is low. We won’t be informed that, as Harvard psychiatrist Joseph Glenmullen wrote in Prozac Backlash, “We do not yet have proof either of the cause or the physiology for any psychiatric diagnosis. . . . In recent decades, we have had no shortage of alleged biochemical imbalances for psychiatric conditions. Diligent though these attempts have been, not one has been proven.”

The ineffectiveness of psychiatric drugs won’t be mentioned -- nor the stream of warnings that have issued from the FDA and international agencies over the past several years concerning the dangerous and often lethal side effects of antidepressants, antipsychotics and stimulants.

We won’t hear about last year’s study of antipsychotics, published in the New England Journal of Medicine, which found the newer antipsychotics to be no more effective than the older drugs. In the study 74 percent of patients quit the drugs and “[T]he majority of patients in each group discontinued their assigned treatment owing to inefficacy or intolerable side effects or for other reasons.” (Note: They didn’t quit because they “decompensated,” “lacked insight,” or were “in denial.” The drugs were ineffective and intolerable.)

Instead, our government will tell us of the terrible consequence of failing to seek treatment. We’ll be told to get branded -- and encourage our friends and family to do the same - as soon as possible. We’ll be assured that life on the pill plantation is a wonderful thing.

The pitch will touching and benevolent, the unspoken message crystal clear: psychiatric stigmatization is a good thing. Only the ignorant and uncaring fail to embrace it. You’ll be hearing a lot about the stigma of mental illness in the coming months and with good reason. A trillion dollar industry depends on it.

For the past 20 years, Richard A. Warner has been the president of the Citizens Commission on Human Rights of Seattle. He's written several pieces for the Seattle Times and Seattle Post-Intelligencer over the years, been a guest on dozens of local and national radio shows, and testifies regularly at the Washington State capital in Olympia on issues related to mental health. His recent paper on shock treatment can be found at ect.org.

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Codex Alimentarius Part II

December 2nd 2006 20:15
Dr. Rath is a highly successful physician who trained under double Nobel-Prize winner Linus Pauling, Ph.D.

Dr. Rath is a physician to be taken seriously. He has produced breakthrough medical research, published books on medicine, and is actively campaigning to bring better health to the world through his research findings in Cellular Medicine. He has produced many breakthroughs in Cellular Medicine - such as an effective cure for heart disease - and he means business when he fiercely and courageously speaks out against the corruption of the pharmaceutical industry.

Dr. Rath is a passionate defender of health freedom in Europe and honest critic of Codex Alimentarius.

Here is a report of what Dr. Rath had to say about Codex at a large health seminar in Bonn, Germany (this was back in November 2004):

"Dr. Matthias Rath left no doubt about who is responsible for the Codex plans: none other than the pharmaceutical cartel, which for countless years has been promising health but spreading illness. The profits of the pharmaceutical investment industry depend on the continued survival and expansion of its markets in patented drugs, genetically modified foods and synthetic food additives - despite the fact that there is an alternative to ineffectual pharmaceutical medicine, embodied in scientifically based, effective natural remedies without side effects, such as Cellular Medicine."

If Enron Could Do It, So Can the Pharmaceutical Industry
"... a single overarching conspiracy to enrich themselves..."

- Prosecutor at trial of former Enron CEOs, Jeffrey K. Skilling and Kenneth L. Lay

If you find Dr. Rath's conclusion that Codex is a tool for profit by the pharmaceutical industry hard to accept, you may need to be reminded that big business has, more than once before, wrought havoc with people's lives and the environment for the sake of greedy self-interest.

One of the best examples of corporate rampage is Enron. Remember Enron? Sure you do.

Enron, one of the largest corporations in the history of America (a titan in the energy industry and the second largest client of accounting giant Arthur Andersen), spectacularly wrecked the lives of thousands of employees by destroying the value of their investments. Enron, it is generally agreed, brought itself down by the sheer weight of the greed of its corporate executives.

The interesting thing is that Enron was being hailed as a success story by the mass media up to the last minute before its spectacular fall!

The pharmaceutical industry is far ahead of Enron on the greed-curve.

According to Marcia Angell, M.D., former editor of the New England Journal of Medicine (one of the world's most prestigious medical journals), the pharmaceutical industry is "a vast marketing machine that thrives on monopoly rights and public-sponsored research but produces few innovative drugs."

It shouldn't be hard to believe that Codex Alimentarius has fallen into the hands of greedy multi-national pharmaceutical corporations, when the spectacular fall of Enron here at home so clearly demonstrates that the corruption of big business is not bound by limits.

Public Relations Deceiving You About Codex
The public relations officers of the pharmaceutical industry are getting paid millions of dollars to project fine-tuned images of morality and clean-play onto the public. No, not everything pharmaceutical companies do is "bad", but many of their products are not in the best interest of your long-term health. The pharmaceutical industry is obsessed with marketing to produce the perception that their products are good for your health.

You will notice a lot of advertising for pharmaceutical drugs in today's society. Everywhere you go, every channel you tune into, there seems to be an ad for drugs. Ads presenting you with picture-perfect images of beneficent companies that are gallantly serving humanity in a free enterprise playground. One must be careful not to fall for the calculated images created by PR, which have no correspondence to the reality of what is going on within these corporations.

Enron was a small-timer compared to the size of the pharmaceutical companies. The top ten companies in the pharmaceutical industry make more in profits than the rest of the Fortune 500 combined!

This means there is ample room in the pharmaceutical industry for a tremendous amount of foul play.

Codex Unscientifically Considers Nutrients as Toxins
The Codex Alimentarius Commission says its standards and guidelines are "scientific". But in truth they are engaged in mad science, not valid science.

Here's why:

The Codex Alimentarius Vitamin and Mineral Guideline uses Risk Assessment to (supposedly) assess "safe" upper limits for vitamins and minerals. Risk Assessment is part of the science of toxicology which is properly applied to substances such as arsenic, lead, mercury, pesticides and other poisons.

But while Risk Assessment is the right science for assessing toxins, it is the wrong science for assessing nutrients!

Nutritional science is a part of Biochemistry, which deals with the metabolism of things like vitamins, minerals, fats, proteins and carbohydrates.

Using Risk Assessment instead of Biochemistry to assess nutrients leads to false data. And false data results in junk science.

Codex is using Risk Assessment to set so-called "upper limits" for nutrients which are so low that they are, by intention, without nutritional impact on even the most sensitive human being!

Why Use the Wrong Science? To Deceive You
The Codex Alimentarius Commission (CAC) is using the wrong science for the job of assessing nutrients. It is seeking to deceive the public that it is "scientific" through the use of junk science (applying toxicology to nutrients).

And because many people don't know the difference between toxicology and Biochemistry, and most haven't even heard of "Risk Assessment", a lot of people have bought the nonsense that Codex is "scientific". Codex is not scientific. It has nothing to do with science. It is all about short-sighted economic self-interest.

For example of the type of "science" that Codex is engaged it, the CAC treats Vitamin C with the same logic as arsenic, lead, mercury, mustard gas, or any other deadly poison. Any reasonable person can see that this is unacceptable.

It's Not About Science Anyway
The Codex moneymen do not seem to understand the simple fact that the detoxification organs of the human body have the ability to expel excess nutrients because evolution has had millions of years to perfect our relationship with nutrients. So there is no need to treat nutrients as toxins and set "upper limits".

Toxins on the other hand are in large part products of the Industrial Revolution and thus they are very new to our bodies, and so cannot be handled properly by our detoxification mechanisms. That's why toxins are toxic!

Comparing nutrients and toxins with the same assessment method is not even close to comparing apples and oranges. It is more like comparing crude oil and water! It is like saying that because drinking crude oil will kill you, therefore, drinking water will kill you too, and so let us, in our sheer arrogance and ignorance, put an upper limit on the amount of water you can drink - "to protect you from yourself"! It may sound absurd, but from a scientific point of view, that is exactly how absurd Codex Alimentarius is.

There is not one trace of reason, logic or science in how Codex treats nutrients as toxins.

It is no exaggeration to say that Codex Alimentarius is based on junk science.
The Vitamin and Mineral Guideline
Codex is made up of several different standards for different aspects of food. One of these standards was ratified (i.e. approved and made ready for implementation in WTO-countries) by the Codex Alimentarius Commission in July 2005, in Rome, Italy. The name of this standard is the Codex Alimentarius Vitamin and Mineral Guideline.

The intention behind the global push for the Vitamin and Mineral Guideline is to allow the legal restriction of natural health products. It has nothing to do with "consumer protection" as claimed. It is all about banning nutritional supplements from the market so that you will be forced to choose the drugs of the pharmaceutical industry.

Example of Vitamin and Mineral Guideline Harm: Forbidding Vitamin C Above 200mg/Day
"It is not only vain, but wicked, in a legislator to frame laws in opposition to the laws of nature, and to arm them with the terrors of death. This is truly creating crimes in order to punish them."

- Thomas Jefferson

Codex Alimentarius would make Vitamin C above 60-200mg per day illegal (the exact limits have not yet been set). If Codex is implemented in the U.S., Vitamin C of doses higher than a tiny amount would become as illegal as the hard drug heroin! And junk science (toxicology for nutrients) would be used to set the dosage.

Vitamin C is one of the most widely used anti-oxidants in the world. It has been proven effective in treating many health conditions. It is a highly affordable substance and is available in abundance on the marketplace. There are no known deaths from Vitamin C. There are well over 3500 scientific articles on the use of Vitamin C in the prevention and treatment of diseases and illnesses ranging from arthritis through cancer and scurvy to cardiovascular disease and a host of other serious conditions.

Linus Pauling, Ph.D., won the first of his two Nobel Prizes for his work on Vitamin C.

It is clear that making Vitamin C above a certain dosage illegal (even with a doctor's prescription) has nothing to do with people's health and everything to do with preventing people from having access to products that compete with the drugs of the pharmaceutical industry.

Why Not Just Ban it Completely?
Why not ban Vitamin C altogether? The Codex people are smarter than that. If they moved too fast, then you and others would see the truth about Codex Alimentarius (that it has nothing to do with consumer protection), and the deceptive veil of "consumer protection" intended to protect the Codex moneymen from being caught red-handed, would be torn down in a heartbeat.

Vitamin C Limit Is Just One Example of Codex Harm
With the restriction on Vitamin C in place, you would no longer be able to rely on this important nutrient to help you through colds. For more serious immune problems, you would no longer be able to use Vitamin C in high dosages.

But obstructing your access to Vitamin C is only one example of what Codex would severely restrict. Virtually every other supplement and traditional remedy would either be banned, or reduced below therapeutic dose levels (using the wrong science of toxicology to set meaningless "upper limits").

Who is Responsible for Codex Alimentarius?
Codex is a joint project of the World Health Organization and the Food and Agriculture Organization and is the result of a complex relationship between:

United Nations - which created the Codex Alimentarius Commission as a trade committee
World Trade Organization - which can enforce Codex Alimentarius Guidelines, Regulations and Standards through coercive trade sanctions
World Health Organization - a UN body which is actively contributing to creating Codex Alimentarius regulations despite the fact that Codex directly and explicitly conflicts with WHOs own findings on global death through under-nutrition (the findings conclude that nutritional supplementation in high dosages are important to World health - Codex would ban these supplements in high dosages and thus goes against WHO's own findings!)
Food and Agriculture Organization - another UN body, which is also going against the findings of WHO because of its support for Codex
Our FDA and USDA
We have been ingrained, mentally and emotionally, with the message that the above institutions are working "for the good of all". Their involvement in the Codex problem may make it seem benign.

But while there are good people in these organizations, the organizations themselves are not working in a benign fashion. They are actively working in concert with representatives of the pharmaceutical, pesticide, chemical, industrial agriculture, and biotechnology industries to push Codex Alimentarius onto the unsuspecting people of the world.

"HARMonization" - Bulldozing National Laws with Codex Standards
How is Codex implemented in a country?

It happens through a process called "harmonization". This is an Orwellian term.

There is nothing harmonious, sweet or benign about Codex. We like to call it "HARMonization".

The process of how Codex becomes enforceable in a country could just as well be called "coercion", and this would be more accurate. The coercion comes from the World Trade Organization.

WTO - The Engine Behind Codex
Here's how Codex "happens" in a country: the Codex Alimentarius Commission ratifies proposed standards or guidelines which are presented to it once they reach Step 8 of the development process. Standards and guidelines are developed through the action of one of the Committees of the Commission over a period of years. Until a standard or guideline is ratified it has no standing or impact on either international trade or national law.

Once a Codex standard or guideline is ratified it is not a law per se. The way it works is that it serves as the standard or reference by which international trade disputes are settled through the dispute resolution process of the World Trade Organization.

The WTO can take a country to court in its own courts, as the WTO has done several times in the U.S., winning each time, to force that country to change its sovereign laws or face severe economic punishment (sanctions)! This is a decidedly undemocratic process.

Codex never actually becomes "law" - it simply forces itself upon a nation by way of the WTO's sanctioning powers, and through the passing of pro-Codex bills by traitorous insider politicians who play the hands of the Codex moneymen.

Without the coercive powers of the World Trade Organization, Codex is just ink on paper, all 200,000 pages sitting somewhere collecting dust.

Our Unique and Powerful American Defense
Are we doomed to Codex takeover? No. If we, the people, act decisively and in massive numbers, and our Congress acts to protect the people from Codex, we are not doomed at all.

In the U.S., we have a powerful legal tool on the side of health freedom that many other countries don't have. We have the Dietary Supplement Health and Education Act (DSHEA) which protects nutrition and health freedom from Codex. DSHEA mandates that nutritional supplements be classed as foods, not drugs, and thus no upper limit may be set for them (which would make the upper limits of Codex illegal). DSHEA was passed in 1994 after grass-roots pressure by millions of Americans, and it is the law of the United States of America unless it is destroyed by the interests behind Codex.

U.S. Codex Office Policy on Codex Alimentarius is Illegal
The U.S. government supports the restrictive, illness-promoting Codex Alimentarius Vitamin and Mineral Guideline (VMG), despite the fact that this position is illegal under U.S. law!

The pro-Codex position of the U.S. Codex Office is illegal because Title 19 USC 3512 prohibits America from harmonizing with any international standard that violates U.S. laws. The Codex Vitamin and Mineral Guideline would violate DSHEA (the 1994 law which treats supplements as foods).

As a result of DSHEA, no upper limit can be set for nutrients in the U.S. and thus Codex would violate DSHEA (because Codex would set upper limits for nutrients using the wrong science of Risk Assessment).

U.S. Codex Office Has Been Notified About its Illegal Position
The U.S. Government was notified that it is illegal for the U.S. Codex Office to support ratification of the Codex Alimentarius Vitamin and Mineral Guideline (VMG) by a Citizen's Petition produced by the Natural Solutions Foundation (sponsor of HealthFreedomUSA.org), submitted on June 1, 2005.

A Citizen's Petition is not a conventional petition. It is a powerful legal tool to compel action on the part of the U.S. Government to follow its own laws and to lay the groundwork for further legal action if the Government does not change course.

Despite our emergency Citizen's Petition, Dr. Ed Scarbrough, head of the U.S. Codex Office, unfortunately announced that the U.S. Codex Office has chosen to stand firm on its illegal pro-illness, pro-Codex Vitamin and Mineral Guideline position, which was ratified in Rome, Italy, on July 4, 2005.

The Natural Solutions Foundation (the organization behind HealthFreedomUSA.org) will be taking the U.S. Codex Office to court.

Napoleon Bonaparte and Codex Alimentarius
If you thought what you've read so far was interesting, this is where the whole Codex issue gets really interesting:

What hardly anyone talking about Codex ever mentions is that it is based on the Napoleonic Code. Most people are not aware of the Napoleonic Code, so let's explain what it is and why the Napoleonic Code is not the freedom-lover's best friend.

The Napoleonic Code - brainchild of the emperor with the same name - conflicts with Common Law (upon which American law is based).

The most notable conflict between the Napoleonic Code and Common Law is that everything that is not explicitly permitted is prohibited by default under the Napoleonic code while everything that is not explicitly prohibited is permitted (i.e. unregulated) under Common Law unless proven harmful by the law.

The Napoleonic Code does not suit a society where the value of individual liberty demands that everything remain legal unless proven harmful to the community.

Under Codex, because of its Napoleonic underpinnings, everything would have to first be approved by the regulatory body before you could legally use it; otherwise you are forbidden from using it.

So, for example, if we have apples, and apples are not explicitly permitted by the government agencies and organizations responsible for implementing Codex rules (FDA, USDA, DOT, HHS, DOC, EPA, etc. here in America), then apples would be illegal to sell, buy and use under Codex!

That is, in a nutshell, the legal aspect of how Codex operates.

Does this sound like a tyrannical scheme?

It sounds like a tyrannical scheme - because that's exactly what it is!

Codex Would Mean Destruction of Supplement Manufacturers and Health Food Stores
All new and innovative remedies and nutrients would be forbidden by Codex. They would be forbidden because they would not be explicitly permitted by Codex so they would not even be allowed on the market. Remember: anything not permitted as part of the list of Codex-allowed nutrients would simply be illegal.

Manufacturers would stop producing new and innovative nutritional supplements because they wouldn't be allowed to manufacture such nutrients, since they would be illegal.

Health food stores would stop carrying non-Codex nutritional products because they would not be able to sell them (remember: it would be illegal). Health food stores wouldn't even have manufacturers to supply them with products to sell since the manufacturers would be out of business!

The only legal products would be those on the Codex "positive" list (i.e., what Codex allows).

And of course, therapeutic dosage natural health products would never be put on the Codex "positive" list, because that's the whole point of the list: to obstruct and thus destroy natural health product competition to the pharmaceutical industry's drugs.

"Tyranny" - It's the Right Word
Codex would allow severe government control over people's health choices. This is tyranny, plain and simple.

Remember Jefferson and the question about what Codex's rightful name is? The answer: Codex is a tool for tyranny for the sake of the interests of greedy multinational corporations.

But it is disguised by its sponsors and supporters as "consumer protection". This disguise is designed to prevent the American people and Congress from taking decisive action to protect health freedom from Codex.

Be Mindful of Subtle Deception
Even supposed defenders of supplements and nutritional products, such as the National Nutritional Foods Association (NNFA) and the Council for Responsible Nutrition (CRN) appear to have fallen prey to the influence of the pharmaceutical industry and are spreading false information saying that Codex is harmless and even good for us.

Codex Brings Devastation to the Earth's Environment

"Pesticides have often been studied for their links to cancer. Populations that are most at risk for pesticide-related cancers include workers with occupational exposure to pesticides, children whose parents have occupational exposure to pesticides, populations living in agricultural areas of heavy pesticide use and children whose parents use pesticides inside and outside of the home."
- Samuel Epstein, M.D.

Codex would encourage the increased use of pesticides, veterinary hormones and other toxic drugs and unlabelled Genetically Modified Organisms (GMOs) in your food.

This is in violation to evidence about the dangers of these substances brought forward by eminent scientists like Dr. Epstein.

Codex would promote the increased use of toxins while responsible physicians and scientists the world over are calling for moratoriums and bans on pesticides, GMOs, and hormones and antibiotics in animals, due to the devastating carcinogenic effects of these toxins!

Codex is way behind the times. It is way behind the findings of real science.

Our Responsibility is to Help Congress Protect America

We need to remind Congress of its duty, namely, to first and foremost protect the well-being and interests of the American people who have elected them. We need to make friends with our Congressmen and Congresswomen. They are going to suffer as much as any other American if our health freedoms are subjugated to the desires of the pharmaceutical industry.

We must remind Congress not to allow itself to be abused as pawns in this reckless chess-game of greedy special interest groups.

At the bottom of this web page is a link to a tool that allows you to contact your local Congress representative via the Internet.

Our Enemies: Deception, Lack of Knowledge and Inaction
No one in their right mind would approve this corporate-sponsored control over health unless they didn't know what was befalling them. Codex cannot be agreed with by any sensible American. It is to be stood up against.

Falling for deception, produced by the Codex-sponsors, is our first enemy.

Lack of knowledge about Codex is our second enemy.

Inaction is our third enemy.

HealthFreedomUSA.org helps you neutralize and overcome the first two enemies so your path to effective action is crystal clear. We've made it easy for you to take action (see bottom of page).

You have the power to make a difference. Therefore, Codex is not your primary enemy. That person in the mirror, if he or she does not act, is your primary enemy. This may sound too strong, but it is the only way to put the reality of the situation openly on the table. We, as the American people, are faced with the opportunity to protect our health freedom and to use Codex as a catalyst to expand health freedom. But we must act.

Taking Action is Easy and Quick
By now you should have no doubt that Codex Alimentarius is good for no-one but certain industries. They are doing just fine without the tyrannical powers Codex would give them, so let us stand firm and protect our health freedom. Our health freedom is certainly worth more than massive increases in the profits of massive multi-national corporations!

The Codex story is not written in stone. We can avert this tool of tyranny. There is a window of opportunity to change the course of health freedom from devastation (Codex-ruled America) to growth and renaissance (in an America protected from Codex).

It's time to take action.

Click here for 3 easy steps that allow you to do your part in protecting health freedom from Codex Alimentarius.
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Codex Alimentarius 101 Part I

December 2nd 2006 19:01
"Because the interests of the Pharma-Cartel are against the health interests of entire mankind, the battle will be fierce; therefore, the Cartel tries to force other industries behind its unethical plans by means of laws."

- Matthias Rath, MD, famous German physician, outspoken critic of Codex Alimentarius


[ Click here to read more ]
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December 2nd 2006 17:15
News You're Not Supposed to Know![
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