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Archive for Natural Solutions Foundation – Page 27

HHS Declares Health Emergencies – And Protects Industry!

By Administrator on October 23, 2008 No Comments

The Natural Solutions Foundation has been deeply concerned for some time now about the possibility, enshrined in Executive Order, Homeland Security Directive, Patriot Actis 1 and HS Declares ‘Health Emergencies’ to Limit Legal Liability for harm done to victims of vaccine injury and other preventable medical disasters. We note with great alarm that the mechanism of “Emergency” declarations is being used with increasing frequency and take this opportunity to share with you a very serious issue which we urge you to take seriously and heed the potentially dire implications of.

Please remember that the Natural Solutions Foundation is the only organization pulling all of these threads together to give you a comprehensive picture of the threats to your health freedom, and our successes in protecting it.

And please give generously to support this organization working hard to keep your health freedom free. Click here (http://drrimatruthreports.com/index.php?page_id=189) to make your tax deductible contribution to health keep freedom free.
Thanks!
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD

Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
www.NaturalSolutionsFoundation.org
www.Organics4U.org
www.NaturalSolutionsMarketPlace.org
www.NaturalSolutionsMedia.tv

http://www.legitgov.org/HHS_declares_health_emergencies.html
HHS Declares ‘Health Emergencies’ to Limit Legal Liability for Anti-
terrorism Vaccines, Drugs
By Lori Price
www.legitgov.org

October Surprises: The U.S. Health and Human Services Secretary,
Michael Leavitt, has declared a series of ‘public health emergencies’
— due to risk of a bioterrorism attack — that continue through 2015.

Oct. 1, 2008: U.S. declares a ‘public health emergency’ due to the
risk of a bioterrorism attack. HHS Secretary, Michael Leavitt, said
the emergency began on Oct. 1 and would run through Dec. 31, 2015.
The declaration establishes legal immunity for public and private
officials who oversee the production or distribution of the anthrax
vaccine.
Oct. 10, 2008: U.S. declares more ‘public health emergencies’ for
smallpox, radiation sickness from the detonation of a nuclear device
and poisoning from botulinum toxins, the active ingredient of Botox.
This move provides the manufacturers, distributors, and others, of
‘anti-terrorism’ drugs and vaccines immunity from lawsuits, should
injuries or deaths occur due to the drugs or vaccines.
U.S. Limits Anthrax Vaccine Legal Liability By Elaine M. Grossman 07
Oct 2008 The U.S. Health and Human Services Department early this
month moved to shield government, industry and business officials
from lawsuits filed by those who have received the anthrax vaccine
(see GSN, Sept. 5, 2007). Health and Human Services Secretary Michael
Leavitt established legal immunity for public and private officials
who oversee the production or distribution of the anthrax vaccine by
declaring a “public health emergency” due to the risk of a
bioterrorism attack. He said the emergency began on Oct. 1 and would
run through Dec. 31, 2015. U.S. law provides protection from lawsuits
to individuals responsible for selected countermeasures, including
antibiotics, during a declared emergency. Under the Public Readiness
and Emergency Preparedness Act, which President [sic] George W. Bush
signed into law in December 2005, a health and human services
secretary’s emergency declaration can limit financial risk for
government program planners and the manufacturers or distributors of
pharmaceutical countermeasures.

Emergency declarations smooth way for vaccine makers –Consumer
advocates see action as giveaway to the drug industry that strips the
public of legal protections. 17 Oct 2008 In a little noticed move,
federal officials this month have declared a series of public health
emergencies relating to potential weapons of biological terror. On
Oct. 1, Health and Human Services Secretary Mike Leavitt declared an
anthrax public health emergency. On Oct. 10, he declared health
emergencies for smallpox, radiation sickness from the detonation of a
nuclear device and poisoning from botulinum toxins, the active
ingredient of Botox. There’s no clear evidence that terrorists have
managed to weaponize anthrax or stolen large caches of Botox from
cosmetic surgeons in Beverly Hills. But by declaring these public
health emergencies, HHS has granted manufacturers of anti-terrorism
drugs and vaccines and others involved with the products protection
from lawsuits if the drugs were to cause unfortunate side effects.

Bogus Anthrax ‘State of Emergency’ Protects Drugmakers, Not Public By
Brandon Keim 15 Oct 2008 Not a single case of human anthrax has been
reported in the United States this year, but the nation is now
officially in a state of anthrax emergency. The emergency was
declared earlier this month by the Department of Health and Human
Services, and will last until 2015. Whether it will protect public
health is debatable, but it will certainly protect makers of faulty
anthrax vaccines. Emergency exemption from legal liability is granted
to vaccine manufacturers by the Public Readiness and Preparedness
Act, passed in 2005 to protect against paralyzing lawsuits during
outbreaks of anthrax, avian influenza or other potentially pandemic
diseases. The act is supposed to be invoked when the Secretary of
Homeland Security has determined “that there is a domestic emergency,
or a significant potential for a domestic emergency, involving a
heightened risk of attack with a specified biological, chemical,
radiological, or nuclear agent or agents.”

37 human anthrax cases in northern Iraq outbreak 12 Oct 2008 Thirty-
seven people have been infected by anthrax in northern Iraq in the
country’s first outbreak of the disease since the 1980s, the health
minister in the Kurdish autonomous region said on Sunday. Health
Minister Ziryan Othman said the disease appeared to have been passed
on from livestock [?]. The first human case of the outbreak was
discovered in remote Dahuk province last month.

US controls bird flu vaccines over bioweapon fears 11 Oct 2008 When
Indonesia’s health minister stopped sending bird flu viruses to a
research laboratory in the U.S. for fear Washington could use them to
make biological weapons, Defense Secretary Robert Gates laughed and
called it “the nuttiest thing” he’d ever heard. Yet deep inside an 86-
page supplement to United States export regulations is a single
sentence that bars U.S. exports of vaccines for avian bird flu and
dozens of other viruses to five countries designated “state sponsors
of terrorism.” The reason: Fear that they will be used for biological
warfare.

Mail carriers, escorted by police, to bring drugs in anthrax attack —
HHS science advisor: Attack using crop-dusting airplane dumping
anthrax spores over a city is a possible scenario 01 Oct 2008
Government mail carriers would deliver emergency supplies of
antibiotics to people in U.S. cities in the case of an anthrax
attack, U.S. Department of Health and Human Services officials said
on Wednesday. The system has been tested in three large [blue] cities
— Seattle, Philadelphia and Boston — and a pilot program is set to
begin soon in the Minneapolis-St. Paul area in Minnesota. The U.S.
Postal Service carriers who would bring the antibiotics from door to
door all would be volunteers who would have advance supplies of
antibiotics to protect themselves and their families, officials said.
Following any new attacks, the mail carriers would be escorted by
local police as they deliver supplies of a few days’ worth of
antibiotics directly to residences throughout an affected community,
HHS Secretary Mike Leavitt said.

HHS Announces New Steps in Anthrax Preparedness (dhs.gov) 01 Oct 2008
HHS Secretary Mike Leavitt today announced two new actions in the
department’s ongoing activities to bolster the nation’s preparedness
for a potential outdoor anthrax attack. In development since March of
this year, the steps being implemented today build upon more than a
decade of preparedness efforts across HHS and other agencies of the
federal government. The first of today’s actions focuses on United
States Postal Service letter carriers who volunteer to deliver
medicines directly to residences in their communities during an
emergency… Over the past several years, under the Cities Readiness
Initiative (CRI), HHS and the Postal Service have successfully
developed and tested in three U.S. cities — Seattle, Philadelphia
and Boston –the ability of letter carriers to quickly deliver door-
to-door quantities of antibiotics from the Strategic National
Stockpile to residential addresses. This quick-strike capability is
intended to buy time for local and State public health authorities to
set up points of dispensing for further provision of antibiotics
across the community.

Judge Affirms Win for Plaintiffs in ‘Anthrax I’ Case By Elaine M.
Grossman 05 Sep 2007 For the first time, a federal judge last month
declared six U.S. defense personnel the definitive winners in a four-
year court battle over the anthrax vaccine. The Aug. 21 decision,
which revolves around payment of attorneys’ fees, is the latest
chapter in a protracted struggle over whether the Defense Department
can require service members to take the anthrax vaccine. U.S.
District Court Judge Emmet Sullivan decided the government defendants
must pay the plaintiffs’ expenses because the plaintiffs won the
case. The litigants — defense personnel who were required to take
anthrax vaccine shots in a Defense Department effort that began in
1998 — won the first round of litigation in October 2004, when
Sullivan issued a permanent injunction banning mandatory
inoculations. Based on a finding that the vaccine was never certified
to protect against “weaponized” airborne anthrax spores, the judge
declared the Pentagon’s mandatory vaccinations “illegal.”

HOMELAND SECURITY PRESIDENTIAL DIRECTIVE/HSPD-21, issued 18 October
2007, states that within one year of the directive’s date, ‘the
Secretaries of Health and Human Services and Defense, in coordination
with the Secretaries of Veterans Affairs and Homeland Security, shall
establish an academic Joint Program for Disaster Medicine and Public
Health housed at a National Center for Disaster Medicine and Public
Health at the Uniformed Services University of the Health Sciences…
Department of Health and Human Services and Department of Defense
authorities will be used to carry out respective civilian and
military missions within this joint program.’

Categories : Blog / Vlog, Disinformation, Events, Get Involved, Miscellaneous, Privacy
Tags : Anthrax, Dr. Rima, Emergency, Health Emergency, MD, Natural Solutions Foundation, NSF, October Surprise, Rima E. Laibow

GM Files: “GMOs are Futile and Dangerous” -Mae Wan Ho, PhD

By Administrator on October 23, 2008 No Comments

Dr. Mae Won Ho is a brilliant and fearless truth teller. Her science is impeccable and her voice is loud and strong when it comes to telling the truth about dangerous make believe science. Nowhere is she more vigorous in alerting us to the absurdities and deadly consequences of corporate junk science and junk policies than in the area of Genetically Modified Organisms or GMOs.

The following article is a must read, must share one which I urge you to forward to as many people as possible so that they can join forces to make sure that all legislators understand that the FDA and USDA are not protecting our interests and Congress must take the reins from them before their criminal negligence kills us all.
The reallity is that stark.

Click here (http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=25920) to urge your legislators to become supporters of the suite of bills introduced by Rep. Denis Kucinich to require safety assessments of GMOs and require clear labeling of all GMO ingredients and components of food.

And then click here (http://drrimatruthreports.com/index.php?page_id=189) to make a tax deductible, recurring donation so that the Natural Solutions Foundation can continue to bring you the facts you need about your health freedom.

Thanks.
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD

Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
www.NaturalSolutionsFoundation.org
www.Organics4U.org
www.NaturalSolutionsMarketPlace.org
www.NaturalSolutionsMedia.tv

GM is Dangerous and Futile
We Need Organic Sustainable Food and Energy Systems Now

New genetics research invalidates the science underpinning the $73.5 billon global biotech industry and confirms why genetic modification is futile and dangerous; we must implement organic sustainable food and energy systems now Dr. Mae-Wan Ho

Invited Lecture at Conference on Future of Food: Climate Change, GMOs and Food Security, 1-2 October 2008, India International Centre, New Delhi

A fully referenced version of this article is posted on ISIS members’ website. Details here

An electronic version of this report with full references can be downloaded from the ISIS online store. Download Now
digg Add to My Yahoo!

I am deeply and doubly honoured to be part of this important conference on Mahatma Gandhi’s birthday, because it was Vandana Shiva and Tewolde Berhan Gebre Egziabher who inspired me and turned me from an ivory tower academic into a science activist. Consequently, I was thrown out of my university and liberated to join civil society in fighting corrupt science and protecting good independent science.
Food Futures Now , *Organic *Sustainable *Fossil Fuel Free, How organic agriculture and localised food, and energy systems can potentially compensate for all greenhouse gas emissions due to human activities and free us from fossil fuels “Change to gene theory raises new challenges for biotech”

The headline appeared in the business section of the International Herald Tribune 3 July 2007 [1]. The article went on to say: “The $73.5 billion global biotech business may soon have to grapple with a discovery that calls into question the scientific principles on which it was founded.”

It was referring to the findings of project ENCODE (Encyclopedia of DNA elements), organised by the US National Human Genome Research Institute. A consortium of 35 research groups went through 1 percent of the human genome with a fine-tooth comb to find out exactly how genes work.

To their surprise, researchers found that the human genome might not be a “tidy collection of independent genes” after all…Instead, genes appear to operate in a complex network, and interact and overlap with one another and with other components in ways not yet fully understood.”

The Human Genome Research Institute said that these findings will challenge scientists “to rethink some long-held views about what genes are and what they do.”

The author of the article Denis Caruso commented that, “the report is likely to have repercussions far beyond the laboratory. The presumption that genes operate independently has been institutionalized since 1976, when the first biotech company was founded. In fact, it is the economic and regulatory foundation on which the entire biotechnology industry is built.” She went on to point out that gene patents and safety assessment based on the same paradigm are also in trouble.

She is right on all counts. I pointed that out 10 years previously when a plethora of findings in molecular genetics had already invalidated the genetic determinist paradigm underpinning the biotech industry. In fact, the paradigm had begun to unravel almost as the industry was starting up twenty years earlier.
The Brave New World of GM Science

In Genetic Engineering Dream or Nightmare, the Brave New World of Bad Science and Big Business [2] first published in 1997/1998 I explained why the science behind GM is wrong and obsolete, and hence dangerous; a story elaborated further in Living with the Fluid Genome [3] published in 2003.

Genetic engineering of plants and animals began in the mid 1970s in the belief that the genome (the totality of all the genetic material of a species) is constant and static, and that the characteristics of organism are simply hardwired in their genome. This was encapsulated in the Central Dogma of molecular biology. The genetic information goes from DNA, the genetic material, to RNA, a kind of intermediate, to protein which determines the characteristic involved, such as tolerance to herbicide, for example. One gene determines one trait, so you can transfer one gene and get exactly the trait you want, be it herbicide tolerance, or resistance to insect pest.

But geneticists soon discovered that the genome is remarkably dynamic and ‘fluid’. It is constantly in conversation with the environment, and that determines which genes are turned on, when, where, by how much and for how long. Moreover, the genetic material itself could also be marked or changed according to experience, and the influence passed on to the next generation. Most of that was known by 1980, long before the Human Genome Project was conceived.

The best thing about the Human Genome Project is to finally explode the myth of genetic determinism [4] (The Myth that Launched a Thousand Companies, SiS 18), revealing the layers of molecular complexity that transmit, interpret and rewrite the genetic texts [5] (Life Beyond the Central Dogma series, SiS 24). The ENCODE project has confirmed and extended the complexities especially with regard to what constitutes a gene. Traditionally, a gene is a sequence of DNA that codes for a protein with a well-defined function. This idea has been well and truly shattered [6]; as Barry Patrick wrote in the Science News [7] “genes are proving to be fragmented, intertwined with other genes, and scattered across the whole genome.”

The genetic engineer’s idea of a gene is presented in Figure 1. It has a regulatory signal, a promoter that says to the cell, go and make lots of copies of the coding sequence that would be translated into a protein, and a terminator that says stop, end of message. This is what genetic engineers put into cells to make a genetically modified organism (GMO).

A gene expression cassette, the genetic engineer’s idea of a gene

Figure 1. A gene expression cassette, the genetic engineer’s idea of a gene

Instead, within the human genome, and indeed other mammalian genomes, coding sequences are in bits (exons) separated by non-coding introns, and exons contributing to a single protein could be in different parts of the genome. Coding sequences of different proteins frequently overlap. Regulatory signals are similarly scattered upstream, downstream, within the coding sequence or in some other distant part of the genome. Coding sequences occupy just 1.5 percent of the human genome, but between 74 and 93 percent of the genome produce RNA transcripts [7], many now known to have regulatory functions. So much so that the project of mapping genetic predisposition to diseases, the original rationale for the Human Genome Project, has now run into serious trouble.

David M. Altshuler, associate professor of genetics and medicine at Harvard Medical School and his research team showed that the risk for type 2 diabetes involves more than a mutated gene. Instead, diabetes, heart disease, some cancers, and other deadly ailments involve non-coding DNA as well as in genes [8]. “We’re realizing that things happening ‘somewhere else’ in the genome, not in genes, are playing critical roles” in sickness and in health, Altshuler said.

David B. Goldstein at Duke University is very pessimistic. He said the effort to nail down the genetics of most common diseases is not working [9]: “There is absolutely no question that for the whole hope of personalized medicine, the news has been just as bleak as it could be. After doing comprehensive studies for common diseases, we can explain only a few percent of the genetic components of most of these traits.” For schizophrenia and biopolar disorder, there is almost nothing, for type 2 diabetes, 20 variants, but they explain only up to 3 percent of familial clustering, and so on.

Goldstein added: “we have cracked open the human genome and can look at the entire complement of common genetic variants, and what do we find? Almost nothing. That is absolutely beyond belief.”

That is just what I predicted soon after the human genome sequence was announced [10, 11] (Human DNA ‘BioBank’ Worthless, SiS 13/14; Why Genomics Won’t Deliver, SiS 26)

Fresh attempts are now made to redefine a gene either in terms of a protein product [12] or a transcript [13], neither of which are satisfactory or would save the industry. All patents on genes based on the old concept are no longer valid; ultimately because the patent is awarded on a supposed function attached to a DNA sequence. But as genes exist in bits interweaving with other genes, so are functions. Multiple DNA sequences may serve the same function, and conversely the same DNA sequence can have different functions. Again, I have explained Why Biotech Patents Are Patently Absurd [14].

Despite the bewildering complexities of how the genome works, individual processes are precisely orchestrated and finely tuned by the organism as a whole, in a highly coordinated molecular ‘dance of life’ that’s necessary for survival.

In contrast, genetic engineering in the laboratory is crude, imprecise and invasive. The rogue genes inserted into a genome to make a GMO could land anywhere; typically in a rearranged or defective form, scrambling and mutating the host genome, and tend to move or rearrange further once inserted. Transgene instability is a big problem, and has been so right from the beginning. There is fresh evidence that GM crops grown commercially for years have rearranged [15, 16] (MON810 Genome Rearranged Again. Transgenic Lines Unstable hence Illegal and Ineligible for Protection, SiS 38). This is a real opportunity to challenge the validity of all biotech patents. Another key issue is safety. Transgene instability means that the original transgenic line has turned into something else, and even if it had been assessed as ‘safe’, this is no longer the case.

The genetically modified genes are a big hazard because they do not know the intricate dance of life that has been perfected in billions of years of evolution. That’s ultimately why genetic modification is both dangerous and futile.
Thirty years of GM are more than enough

We’d had 30 years of GM and more than enough damage done, as detailed in the ISP Report The Case for A GM-Free Sustainable World [17] and the dossier GM Science Expose : Hazards Ignored, Fraud, Regulatory Sham, Violation of Farmers Rights [18] we compiled for the European Parliament in June 2007. And more evidence has been piling up since. Why has this been allowed to go on? W documented how national and international regulators and advisory bodies such as the European Food Safety Authority not only routinely ignore the precautionary principle, but also actively abuse science, sidestep the law, and helping to promote GM technology in the face of evidence piling up against the safety of GM food and feed [19] (GM Food Nightmare Unfolding in the Regulatory Sham, ISIS scientific publication).

Let me summarize the evidence stacked up against GMOs.

* No increase in yields

Successive reports [17, 18, 20] confirm that the yields of all major GM crops varieties cultivated are lower than, or at best, equal to yields from non-GM varieties. Studies from 1999 to 2007 consistently show that GM soya decreased yields by 4 to 12 percent compared to non-GM soya, while Bt maize yields from 0 to 12 percent less than conventional isolines. Up to 100 percent failures of Bt cotton crops have been recorded in India [18] (and amply confirmed by the farmer witnesses who are here today). New research from the University of Kansas found a 10 percent average yield drag for Roundup Ready soya [21], and extra manganese is needed for the soil Scientists from the USDA and the University of Georgia found growing GM cotton in the US could result in a drop in income by up to 40 percent [22, 23] (Transgenic Cotton Offers No Advantage, SiS 38)

* No reduction in pesticides use

USDA data showed that GM crops increase pesticide use by 50 million pounds from 1996 to 2003 in the United States [17]. New data paint an even grimmer picture: the use of glyphosate on major crops went up more than 15-fold between 1994 and 2005, along with increases in other herbicides [24] in order to cope with rising glyphosate resistant superweeds [6]. Palmer 3pigweed is a major concern in Georgia, with farmer there having to mow cotton down in fields with glyphosate-resistant Palmer amaranth [25]. And following close on the health of that is glyphosate resistant giant ragweed [26]. Roundup tolerant canola volunteers are top among the worries of Canadian farmers [27, 28] (Study Based on Farmers’ Experience Exposes Risks of GM Crops, SiS 38)

* Roundup lethal to frogs and toxic to human placental and embryonic cells [18].

Roundup is more toxic than glyphosate, and it is used in more than 80 percent of all GM crops planted in the world.

* GM crops harm wildlife

UK’s farm scale evaluations have found that GM crops harm wildlife [18]; more recently a study led by Loyola University, Chicago, Illinois in the United Stated, found that wastes from Bt corn impaired the growth of a common aquatic insect [29, 30] (Bt Crops Threaten Aquatic Ecosystems, SiS 36). This is just the tip of the iceberg. There is evidence that GM crops, especially Bt crops contribute to the demise of the honeybee worldwide because it compromises their immune system and make them exra-susceptible to attacks by parasitic fungus (31) (Parasitic Fungi and Pesticides Act Synergistically to Kill Honeybees? SiS 35).

* Bt resistance pests and Roundup tolerant superweeds render the two major GM crop traits practically useless [18].

A recent review concluded that [32] “evolved glyphosate-resistant weeds are a major risk for the continued success of glyphosate and transgenic glyphosate-resistant crops.” And the evolution of Bt resistant bollworms worldwide have now been confirmed and documented in more than a dozen fields in Mississippi and Arkansas between 2003 and 2006 [33]. Worse yet, secondary pests now plague the fields and spread to other crops in India [34] (Deadly gift from Monsanto to India, SiS 38).

* Vast areas of forests, pampas and cerrados lost to GM soya in Latin America

Argentina alone has lot 15 m hectares [18]; and this has worsened considerably with the demand for biofuels (see later)

* Epidemic of suicides in the cotton belt of India

An estimated 100 000 farmers have killed themselves between 1993-2003, and a further 16 000 farmers a year have died since Bt cotton was introduced [18]

* GM food and feed linked to deaths and sicknesses

Evidence of serious health impacts in lab tests and from farmers’ fields around the world (more below)
GM food and feed inherently hazardous to health [19]

Here are some highlights from our GM Science dossier [18] on the hazards of GM food and feed. Dr. Irina Ermakova of the Russian Academy of Sciences showed how GM soya made female rats give birth to severely stunted and abnormal litters, with more than half dying in three weeks, and those remaining are sterile. Hundreds of villagers and cotton handlers in India suffer allergy-like symptoms, thousands of sheep died after grazing on the Bt cotton residues, goat and cows as well were reported in 2007 and 2008 [35] (Mass Protests against GM Crops in India , SiS 38). (As reported by farmer witnesses as this conference, the problem is continuing and sterility in offspring of exposed animals has also been observed.) A harmless bean protein transferred to pea when tested on mice cause severe inflammation in the lungs and provoked generalised food sensitivities. Dozens of villagers in the south of the Philippines fell ill when neighbouring GM maize fields came into flower in 2003, at least five have died and some remain ill to this day. A dozen cows died having eaten GM maize in Hesse Germany and more in the herd had to be slaughtered from mysterious illnesses. Arpad Pusztai and his colleagues in the UK found GM potatoes with snowdrop lectin damaged every organ system of young rats; the stomach lining grew twice as thick as controls. Chickens fed GM maize Chardon LL were twice as likely to die as controls. And finally, GM maize Mon 863 was claimed to be as safe as non-GM maize by the company, and accepted as such by European Food Safety Authority. But independent scientists of CriiGen in France re-analysed the data and found signs of liver and kidney toxicity.

Different animals and human beings exposed to a variety of transgenic crops with different traits either fall ill or die. The evidence compels us to consider the possibility that the hazards of GMOs may be inherent to the technology, as I suggested more than ten years ago [2].
Table 1. Summary of Exposure of Animals and Human Beings to GMOs
Species GM species Transgene trait Effect
Rat Soya Roundup Ready Stunting, death, sterility
Humans Cotton Cry1Ac/Cry1Ab Allergy symptoms
Sheep “ “ Death, liver toxicity
Cows “ “ “
Goats “ “ “
Mice Pea Alpha-amylase Inhibitor Lung Inflammation, General food sensitivity
Mice Soya Roundup Ready Liver, pancreas and testis Affected
Humans Maize Cry1Ab Illnesses and death
Rats Maize Cry3Bb liver and kidney toxicity
Cows Maize Cry1Ab/Cry1Ac Death and illnesses
Rats Potato Snowdrop lectin Damage in every organ system. Stomach lining twice as thick as controls
Mice Potato Cry1A Gut lining thickened
Rats Tomato Delay ripening Holes in the stomach
Chickens Maize Glufosinate tolerance Deaths

An epidemic of Morgellons Disease has hit the US and other countries that had been involved in genetic modification technology [36] (Agrobacterium & Morgellons Disease, A GM Connection?. SiS 38). The pathogen is suspected to be Agrobacterium, which has been widely used in smuggling genes into cells to make GMOs. Is this a disease created by GM? There have been close calls before.
US courts rule GM crop field-tests and releases illegal

The message that GM crops are unsafe appears to have got through to the judiciary system in the United States. There have been three court rulings against the US Department of Agriculture (USDA) for failing to carry out proper environmental impact assessment, making the original releases illegal [37] (Approval of GM Crops Illegal, US Federal Courts Rule, SiS 34). These are the first rulings against GMOs in the top producing country in the world, which has been also promoting GMOs aggressively.

The first case was on drug-producing GM crops in Hawaii. The court said that the USDA violated the Endangered Species Act as well as the National Environmental Policy Act.

The second court case not only ruled GM herbicide-tolerant creeping bentgrass illegal, but also that the USDA must halt approval of all new field trials until more rigorous environmental reviews are conducted.

The third decision was passed on Monsanto’s Roundup Ready alfalfa for having been commercial released illegally without an Environment Impact Statement.
An avalanche of bans and rulings strikes GM crops worldwide

There have been numerous bans and restrictions imposed on GM crops in recent years, which say a lot about the inadequacies of regulatory regimes worldwide (see Box 1).

Box 1
Rulings and bans on GMOs between May 2007 and May 2008

* US GM alfalfa ban made permanent [38]
* US Federal Court of Appeals ruled against GM bentgrass again [39]
* Four counties in California have bans or moratorium on GM crops and the first state bill to protect Californian farmers against lawsuits that intimate and harass them when their field are contaminated passed through the Agriculture committee in January 2008 [40]
* Montville USA became the first town outside California to ban GM crops [41]
* South Australia extended its GM ban [42]
* Romania joined EU members in banning GM crop Mon 810 [43], the others are France, Hungary, Italy, Austria, Greece, and Poland
* 13 out of 20 counties in Croatia have declared themselves GM-Free [44]
* Greece renewed its ban on GM maize seeds [44]
* Germany imposed much stricter regulations on GM maize [46]
* Scotland backs GM ban in Europe [47]
* France banned GM maize Mon 810 in February 2008 and passed GMO law in April to guard against contamination by GMO, making it compulsory for farmers to “respect agricultural structures, local ecosystems and non-GMO commercial and production industries” [48, 49]
* Wales is set to ban GM crops [50]
* Switzerland bans crops until 2012 [51]
* More than 230 regions, over 4 000 municipalities and other local entities and tens of thousands of farmers and food producers in Europe have declared themselves GMO-free so far [52]

EU Commissioner for the Environment Stavros Dimas has expressed serious reservations concerning GMOs [53] (GM-Free Europe Beginning?, SiS 36), which is unprecedented in the history of the European Commission. On 7 May 2008, the European Commission delayed a decision on allowing farmers to grow more GM crops, and asked European Food Safety Authority to reconsider its previous review, which it had admitted was inadequate, as it was unable to take indirect and long term impacts into account [54].
No case for GM crops, small scale organic farming is the way ahead

Meanwhile, on 15 April 2008, 400 scientists of the International Assessment of Agricultural Science and Technology for Development (IAASTD) released its 2 500-page report [55, 56] (GM-Free Organic Agriculture to Feed the World”, SiS 38) that took 4 years to complete. It is a thorough examination of global agriculture on a scale comparable to the Intergovernment Panel on Climate Change.

The IAASTD calls for a fundamental change in farming practice to counteract soaring food prices, hunger, poverty and environmental disasters, it says GM crops are controversial with respect to safety for health and the environment, and will not play a substantial role in addressing climate change, loss of biodiversity, hunger and poverty. Small scale farmers and agro-ecological methods are the way forward, and indigenous and local knowledge are as important as formal scientific knowledge. It warns that growing crops for biofuels could worsen food shortages and price rises.

The conclusions of the IAASTD are remarkably similar to our own report Food Futures Now *Organic *Sustainable *Fossil Fuel Free [57] launched in UK Parliament a week later.

Our Food Futures Now report goes a step further. We argue that only organic agriculture can truly feed the world. More than that, organic agriculture and localised food and energy systems can potentially compensate for all greenhouse emissions due to human activities and free us from fossil fuels, and we need to implement this urgently.

The UN has declared 2008 the year of the Global Food Crisis, and it has been the top news story everyday for months now as the crisis deepens. Food prices increased by an average of 40 percent last year; a string of food riots and protests spread around the world including the UK, and more than 25 000 farmers killed themselves in India.

Most commentators agree that the immediate cause of the food crisis is the divestment of food grains into producing biofuels. BusinessWeek identified Monsanto as a “prime beneficiary”. Its stock correlated closely with the price of oil (better than ExxonMobile), and hardly correlated with the price of corn, basically because no one will eat its GM corn. Nevertheless the pro-GM lobby are out in force, using the food crisis to promote GM crops.

GM crops are one big failed experiment based on an obsolete scientific theory, and this failure has been evident since 2004 if not before [58] (Puncturing the GM Myths, SiS 22). Apart from yielding less and requiring more pesticides, anecdotal evidence since 2005 from farmers around the world indicates that GM crops also require more water [59]. Industrial Green Revolution agriculture is now generally acknowledged to be a major driver of climate change as well as being vulnerable to climate change because of its heavy dependence on fossil energies and water, and its susceptibility to pests, diseases and climate extremes [56, 60, 61] (Beware the New “Doubly Green Revolution”, SiS 37)..GM crops have all the worst features of industrial Green Revolution varieties exaggerated, and not least, there are outstanding safety concerns as I mentioned. Growing GM crops for biofuels does not make them safe, as they will contaminate our food crops all the same.

Any further indulgence in GMOs will surely damage our chances of surviving global warming. We must get on with the urgent business of building organic, sustainable food and energy systems right now.

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Categories : Activism, Blog / Vlog, CODEX Consequences, CODEX Industries, Disinformation, Food Crisis, Get Involved, GMOs, Medical Hazards, Miscellaneous, Organics
Tags : Denis Kuchinic, Dr. Rima, Frankenfood, Genetically Modified, GMO, GMOs, Mae Wan Ho, mandatory labeling, MD, Natural Solutions Foundation, NSF, Rima E. Laibow

Evidence of poison: New Levels of Compulsory Drugging – MSG Sprayed on Your Food!

By Administrator on October 23, 2008 No Comments

There are two articles which follow this introduction which have great bearing on your health and, eventually, your ability survive.
Agricultural chemicals have been known since their inception to pose significant threats to human, animal and environmental health. They are, in fact, only approved for use on the food supply of people and animals because, in my opinion, of the enormous wealth which chemical companies, which are, in essence, a branch of the pharmaceutical industry, have have available to throw at compliant regulators and legislators, plus deceptive and misleading advertising bulwarked by corporate junk science.

Agricultural chemicals are not, however, limited to herbicides, fungicides, pesticides and fertilizers. Other chemicals quality for that designation, too. For many years, the US has permitted the spraying of fluoride and mercury on crops after harvest to prevent mold growth during storage despite the well characterized dangers of those substances.
Now, another toxin, also well known for its adverse effect on the brain, the nervous system, the endocrine system, perception, mood and vascular integrety has been approved by the supposed guardians of our health, the FDA, EPA and USDA for direct application, without any upper limit, on our foods.

Read this article and ask yourself whether you ever want to eat non organic food again. Then ask yourself why regulators are permitting known toxins in our food.

And then click on this link (http://drrimatruthreports.com/index.php?page_id=189) to make a donation to the Natural Solutions Foundation, a totally donation-supported Non governmental organization (NGO) devoted to your right to make your own choices in your health. Among the freedoms that we believe belong to you and that we are fighting for on your behalf, and ours, is the right to know what your food has been sprayed with, genetically modified with, contaminated with or irradiated with. In short, if food is contaminated you have a right to know it.
And you have another right, too, as I see it.
You have a right to be protected by the regulators from the self-interested companies that do not care at all about the damage their chemicals and processes bring to you and yours. That is, after all, what we believe regulatory agencies are supposed to do. But the sad truth is that we need to be protected FROM the regulatory agencies.
That’s one of the things that Natural Solutions Foundation does, in fact. And, of course, we need your help. Click here (http://drrimatruthreports.com/index.php?page_id=189) to become a supporting sponsor with a tax deductible recurring donation. And visit the Natural Solutions Foundation home page, www.HealthFreedomUSA.org, to sign up for our free, secure Health Freedom eAlerts.

Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD

Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
www.NaturalSolutionsFoundation.org
www.Organics4U.org
www.NaturalSolutionsMarketPlace.org

MSG is being sprayed right on fruits, nuts, seeds, grains, and vegetables as they grow —
even those used in baby food

In the 1970s, reluctant food processors “voluntarily” took processed free glutamic acid (MSG) out of baby food. Today it’s back, in fertilizers called “Omega Protein Refined/Hydrolyzed Fish Emulsion” and “Steam Hydrolyzed Feather Meal,” both of which contain hydrolyzed proteins; and in a product called AuxiGro WP Plant Metabolic Primer (AuxiGro) produced by Emerald BioAgriculture (formerly Auxein Corporation), which contains both hydrolyzed protein(s) and “monosodium glutamate.” AuxiGro is being sprayed on some of the vegetables we and our children will eat, into the air we and our children must breath, and onto the ground from which it can move into drinking water. Head lettuce, leaf lettuce, tomatoes, potatoes, and peanuts were among the first crops targeted. On September 12, 2000, the Auxein Corporation Web site gave the following information:

Crops registered include: Celery; Fresh Market Cucumbers; Edible Navy and Pinto Beans; Grapes; Bulb Onions; Bell, Green and Jalapeno Peppers; Iceberg Head Lettuce; Romaine and Butter Leaf Lettuce; Peanuts; Potatoes; Snap Beans; Strawberries; Processing Tomatoes; Fresh Tomatoes; and Watermelons.

Today, there is no crop that we know of that has not been approved for treatment with MSG by the U.S. Environmental Protection Agency (EPA).

Even in California — the only state where there are any restrictions on the use of AuxiGro — AuxiGro has been approved for use on a number of crops, and Emerald BioAgriculture continues to push for more. Field tests in California have been — and may continue to be — conducted on a variety of crops, and those AuxiGro treated crops may be sold in the open market without revealing that they have been treated. We can’t tell you which crops those are because the CDPR has refused to send records of test trials (which are public information) to the Truth in Labeling Campaign.

As of June 13, 2002, AuxiGro was registered for use in California on tomatoes, almonds, apricots, cherries, plums, nectarines, peaches, prunes, grapes (including grapes to be used in wine), and onions. At that time, the California Department of Pesticide Regulation said they were not aware of any testing of AuxiGro for use on other crops. They also said that they did not have any proposals presently in house to register additional crops for AuxiGro. It would appear, however, that what the CDPR said was not true, for the CDPR subsequently announced that Emerald BioAgriculture had applied for permission to use AuxiGro on tomatoes (new use), and on melons (new crop) — and, to the best of our knowledge, approval is always preceded by field testing.

On July 7, 2004, Emerald BioAgriculture requested approval of use of AuxiGro as a desiccant, disinfectant, fertilizer, fungicide, growth regulator – for increased yield and prevention of powdery mildew in various crops such as almonds, grapes, and melons. They also asked to add cole crops (including broccoli, brussels sprouts, cabbage, cauliflower, kale, collards, turnips, rutabaga, mustard, watercress, and kohlrabi) to the list of crops approved for AuxiGro use.

Approval for use on organic crops–in all states–has been requested.

What’s wrong with using glutamic acid, an amino acid found in protein, as a spray on crops?

– In protein, amino acids are found in balanced combinations. Use of free glutamic acid as a spray on crops throws the amino acid balance out of kilter.

– It’s not the glutamic acid found in protein that is being sprayed on crops, it’s a synthetic product. The spray being used most widely is called AuxiGro. The “free glutamic acid” or so called “L-glutamic acid” component being used by its manufacturer, Emerald BioAgriculture, contains L-glutamic acid, an amino acid found in protein; but it also contains D-glutamic acid, pyroglutamic acid, and other chemicals referred to in the industry as “contaminants.” The free glutamic acid used in AuxiGro is processed free glutamic acid. It is manufactured — in chemical plants — where certain selected genetically engineered bacteria — feeding on a liquid nutrient medium — excrete the free glutamic acid they synthesize outside of their cell membrane into the liquid medium in which they are grown. In contrast, the free glutamic acid found in protein, and the free glutamic acid involved in normal human body function, are unprocessed. free glutamic acid, and contain no contaminants.

– No one knows what the long term effects of spraying processed free glutamic acid on crops will be.

– That the processed free glutamic acid (MSG) will be absorbed into the body of the plant and into the fruit, nuts, seeds, or vegetable it produces seems undeniable. If it were not, the plant would not be stimulated to grow. Neither Emerald BioAgriculture or the EPA will address this issue.

– That there will be residue left on crops has not been disputed by Emerald BioAgriculture. But no study of either the amount of that residue, or the least amount of processed free glutamic acid needed to cause a reaction in an MSG-sensitive person, has ever been done. “It should wash off” doesn’t mean it will wash off. “It seems unlikely that such a small amount would cause a reactions” doesn’t mean that a small amount will not cause a reaction or have long term health effects.

– Free glutamic acid is known to be toxic to the nervous system. But the neurotoxic effects that processed free glutamic acid will have on animals that consume the plants on which it is sprayed – effects over and above any effects caused by external glutamic acid residue – have never been evaluated. Neither are there data on the effects that spraying processed free glutamic acid will have on drinking water.

– Consider, also, that children are most at risk from the effects of processed free glutamic acid. Their undeveloped blood-brain barriers leave them most at risk from exposure to processed free glutamic acid. It has been repeatedly demonstrated that infant animals fed processed free glutamic acid when young develop neuroendocrine problems such as gross obesity, stunted growth, and reproductive disorders later in life, and that they also develop learning disabilities. Emerald BioAgriculture did not address that particular safety issue in its application to the EPA.

– No one knows how little glutamic acid is needed to kill a single brain cell or to trigger an adverse reaction.

– Free glutamic acid is a neurotransmitter. It causes nerves to fire, carrying nerve impulses throughout the nervous system.

– Free glutamic acid is a neurotoxin. Under certain circumstances, free glutamic acid will cause nerves to fire repeatedly, until they die.

– Processed free glutamic acid kills brain cells. The free glutamic acid ingested by laboratory animals that caused brain lesions and neuroendocrine disorders was very often given in the form of the food ingredient “monosodium glutamate.” “Monosodium glutamate” is the name of a particular food additive. Processed free glutamic acid is the reactive component in “monosodium glutamate,” just as processed free glutamic acid is a reactive component in AuxiGro.

The glutamate industry research done in the 1970s that was submitted to the EPA by the Auxein Corporation, that pretended to find that processed free glutamic acid is “safe,” has been long refuted by independent scientists. Indeed, at the present time, neuroscientists attempting to develop drugs to block the toxic effects of free glutamic acid are using processed free glutamic acid to selectively kill certain kinds of brain cells.

– Processed free glutamic acid causes neuroendocrine disorders in maturing animals that ingest processed free glutamic acid early in life.

– Processed free glutamic acid causes learning disorders in maturing animals that ingest processed free glutamic acid early in life.

– Processed free glutamic acid crosses the placental barrier and causes learning disabilities in animal offspring of dams that ingest it.

– Processed free glutamic acid has access to the brain through the blood-brain barrier, which is not impervious to the unregulated flow of processed free glutamic acid. The blood-brain barrier is immature at birth and may continue to develop up to puberty. In certain areas called the circumventricular organs, the blood barrier is never impervious to the unregulated flow of free glutamic acid. In addition, the blood-brain barrier is easily damaged by such events as high fever, a blow to the head, drug use, stroke, ingestion of processed free glutamic acid, and the normal process of aging.

– The National Institutes of Health recognize glutamic acid as being associated with addiction, stroke, epilepsy, degenerative disorders such as Alzheimer’s disease, Parkinson’s disease, and ALS, brain trauma, neuropathic pain, schizophrenia, anxiety, and depression.

– For years, free glutamic acid has been produced and used in food additives with names such as monosodium glutamate, sodium caseinate, and hydrolyzed soy protein. In some people, the processed free glutamic acid in food additives causes adverse reactions that include migraine headache, asthma, arrhythmia, tachycardia, nausea and vomiting, depression, and disorientation. The processed free glutamic acid in prescription and non-prescription drugs, food supplements, and cosmetics can also cause adverse reactions.

There are badly flawed industry-sponsored studies that have pretended to find that processed free glutamic acid does not cause adverse reactions. Inappropriate procedures used by the glutamate industry have included limiting subjects to people virtually guaranteed not to be sensitive to processed free glutamic acid, and/or using processed free glutamic acid or other similarly reactive substances in placebos as well as in test material. The Food and Drug Administration (FDA) has based its claim that processed free glutamic acid causes only mild and transitory reactions on those badly flawed industry-sponsored studies.

– Even the EPA admits that the food additive called “monosodium glutamate” causes adverse reactions.

– Even the FDA admits that the food additive “monosodium glutamate” contains processed free glutamic acid.
<>– Even the FDA admits that many consumers refer to all free glutamic acid as “MSG.”

The EPA’s approvals of use of MSG in agriculture are simple, straightforward, and in violation of the Federal Food, Drug, and Cosmetic Act

In reviewing the application of Auxein Corporation (now Emerald BioAgriculture) for use of processed free glutamic acid in a spray to be applied to crops as they grow, the EPA failed to conform to the requirements of the Federal Food, Drug and Cosmetic Act, which require, in part, that the EPA review any proposed action for validity, completeness, reliability, and relationship to human risk. The EPA also ignored Executive Order 13045 which requires government agencies to consider available information concerning the variability of the sensitivities of major identifiable subgroups of consumers, including infants and children. For example, Auxein Corporation sent the EPA 14 industry-sponsored toxicological studies from the literature, all done in the 1970’s, but failed to mention hundreds of studies in the literature that refuted those 14 studies. Auxein Corporation even failed to send the EPA independent studies that appeared in the same book(s) as the industry-sponsored studies sent to the EPA. For example, although processed free glutamic acid causes brain lesions and neuroendocrine disorders in infant animals, this special hazard faced by infants was ignored by Auxein Corporation. It would appear that Auxein Corporation restricted its consideration of “available information” to information made available by the glutamate industry; and the EPA, even after having been sent abstracts from other “available information,” has not challenged the Auxein Corporation applications. A more complete discussion of the shortcomings of the EPA approvals granted to Auxein Corporation has been submitted to the EPA.

Questions about the safety of spraying processed free glutamic acid on plants and into the environment have been raised by the Truth in Labeling Campaign and by individual consumers. The EPA has refused to address those concerns. The EPA, and, in particular, EPA spokesperson Dr. Janet Andersen, has failed to respond to allegations that in approving the spraying of processed free glutamic acid, the EPA failed to consider the reliability, validity, and completeness of the Auxein Corporation application or comply with Executive Order 13045 entitled Protection of Children from Environmental Health Risks and Safety Risks, except to say that the EPA had complied with executive order 13045. Moreover, while responding to letters that asked direct questions of the EPA, Andersen failed to respond to most, if not all, of the direct questions contained in those letters.

AuxiGro, the first MSG-laced plant “growth enhancer” to hit the market, has been approved for spraying on every crop we know of, with no restrictions on the amount of processed free glutamic acid (MSG) that may remain in and/or on crops when brought to market. Even before consumers had an inkling that crops were being sprayed, the Truth in Labeling Campaign received reports that MSG-sensitive consumers had gotten sick from head lettuce and potatoes.

Federal Register notices chronicling the application and approval of processed free glutamic acid are available on the Web via GPO Access, the Federal Register, through: http://www.gpoaccess.gov/fr/index.html. Application for approval of use of AuxiGro was made to the EPA in 1997. Testing of the product was also approved in that year, and many of the test crops sprayed with AuxiGro were brought to market without notifying consumers. Glutamic acid was granted an exemption from establishment of a tolerance limit in January, 1998. AuxiGro was also approved for use on a number of crops in January, 1998, and approved for use on other crops later. No announcement of these approvals was made in the Federal Register.

Due to a technical glitch in the system, the glutes came to need one more approval to make their California registrations work. The glutes were asking for AuxiGro to be approved for use as a fungicide in California, but the EPA had only approved AuxiGro for use as a pesticide produce or plant growth enhancer. And when application was made for this addition to their approvals, the application was brought to our attention; and the Truth in Labeling Campaign filed a formal protest to this approval of AuxiGro. The Formal Objection of the Truth in Labeling Campaign was filed on August 16, 2001 with the EPA.

By law, formal objections filed in a timely manner must be responded to within six months. Also, by law (we were told) even though the Final Rule had not been promulgated, this additional use of AuxiGro would be considered approved unless and until the EPA determined that it should be otherwise. In July, 2004, we received a conference call from Dr. Andersen and a number of other EPA players, including an EPA lawyer — a “courtesy call” telling us that our objections had been discounted and that the Final Rule allowing use of AuxiGro as a fungicide would be published shortly in the Federal Register.

What’s wrong at the EPA?

Neither the EPA nor Janet Andersen, Ph.D., director of the Biopesticides and Pollution Prevention Division (BPPD), are stupid. Rather, all evidence would appear to suggest that the EPA, which is charged with protecting the health of Americans, says it is protecting the health of Americans, when in fact the EPA acts to protect the bottom line of big business. Don’t think for a moment that MSG is the only toxin unleashed on the American public by the EPA. Let the words “methyl parathion” and “DDT” jog your memory.
The EPA, in granting the chemical referred to as “L-glutamic acid” an exemption from the requirement of a tolerance for residues of “L-glutamic acid” on all food commodities when applied/used in accordance with good agricultural practices (thereby allowing unrestricted amounts of processed free glutamic acid (MSG) residue to remain in and on any and all food crops that come under the EPA’s jurisdiction) violated Section 408(c)(2)(A)(i), Section 408(c)(2)(ii), Section 408(c)(2)(B), and Section 408(b)(2)(D) of the Federal Food, Drug, and Cosmetic Act.

Neither “L-Glutamic Acid and Gamma Aminobutyric Acid; Exemptions from the Requirement of a Tolerance; Final Rule” (Federal Register June 21, 2001) nor “Glutamic Acid; Pesticide Tolerance Exemption; Final Rule” (Federal Register January 7, 1998), which preceded it, met the criteria established by law for granting exemptions from the restriction of a tolerance.
How did spokesperson Andersen excuse the fact that the EPA approved processed free glutamic acid for use in an EPA approved spray? First, said Andersen, the free glutamic acid used in the spray is naturally occurring, and it’s 99.3 per cent pure pharmaceutical grade L-glutamic acid. Yet, in admitting that the free glutamic acid in AuxiGro is not 100 per cent pure L-glutamic acid, and that it is pharmaceutical grade, Andersen contradicted herself, and actually made the point that 1) if the free glutamic acid used in AuxiGro were truly natural, it wouldn’t be “pharmaceutical grade;” and 2) if the free glutamic acid used in AuxiGro were truly natural it would be 100 per cent, not 99.3 per cent pure L-glutamic acid.

Andersen said something else very interesting. She said that the EPA is well aware of the fact that MSG causes adverse reactions. However, when Andersen used the term “MSG” she was referring to the one food ingredient called “monosodium glutamate,” and not to the free glutamic acid in “monosodium glutamate” that causes adverse reactions. Failure to define terms, as Anderson did (and does) so handily, is both deceptive and misleading.

What Andersen did is very clever. What she said makes no sense at all. No one has ever claimed that the processed free glutamic acid in AuxiGro comes out of a box labeled “monosodium glutamate.” So for her to say it doesn’t, is meaningless. On the other hand, the claim has been made that the free glutamic acid in AuxiGro will cause the same brain lesions, neuroendocrine disorders, adverse reactions and other diverse disease conditions that are caused by the free glutamic acid in “monosodium glutamate” and the other food additives that contain processed free glutamic acid. That claim is true, but Andersen does not address it. How do you refute someone who ignores legitimate questions and spews out irrelevant statements as though they pertained to your legitimate questions? You don’t. The EPA defense of its approval of use of processed free glutamic acid in plant “growth enhancers” and its registration of AuxiGro has two parts to it: 1) ignoring those who question EPA actions, and 2) making the irrelevant statement that AuxiGro does not contain MSG (monosodium glutamate).

Neither Andersen nor anyone else at the EPA ever addressed the criticism that approvals given by the EPA to allow the use of free glutamic acid and the product AuxiGro were inappropriate.
The EPA, which approved the used of processed free glutamic acid in plant “growth enhancers,” made a grievous error. But instead of recognizing and remedying that error once it was pointed out to them, the EPA began a cover-up. That cover-up included use of ambiguous words and phrases, half-truths, and downright lies told to consumers. The cover-up continued (and continues still) with a variation of those ambiguous words and phrases, half-truths, and downright lies told to legislators who inquire about spraying MSG into the environment.

You might find the Emerald BioAgriculture sales literature interesting

Sales literature promoting AuxiGro was once found on their Web site, but is now long gone. While Federal Register notices included the fact that there is processed free glutamic acid (MSG) in AuxiGro, the sales literature from Auxein Corporation did not mention the fact that their product contains free glutamic acid until the Truth in Labeling Campaign began to broadcast that information. In November, 1999, Auxein added deceptive, misleading, and untrue statements in an elaboration of its Product Page, wherein they essentially make the untrue assertion that the glutamic acid used in AuxiGro is chemically and biologically identical to that found in plants and animals.

Sales literature did (on September 12, 2000), however, contain the following:

“PRECAUTIONARY STATEMENTS

HAZARDS TO HUMAN AND DOMESTIC ANIMALS – CAUTION”

If you think you might be reacting to AuxiGro sprayed on crops, you might want to try to (contact Emerald BioAgriculture (formerly Auxein Corporation) at the addresses that follow. (A friend recently told us that he tried to contact them by e-mail, but his e-mail was returned unopened.) By law, the company is required to forward reports of adverse reactions to the EPA. You might want to ask the EPA if Emerald BioAgriculture did so.

John L. Mclntyre, Ph.D.
President & CEO
Emerald BioAgriculture (formerly Auxein Corporation)
3125 Sovereign Drive, Ste. B
Lansing, MI 48911-4240
Phone: (888) 828-9346
Fax: (517) 882-7521
E-Mail: mailto:%20sales@auxein.com
(From time to time, their web page, http://www.auxein.com , can be accessed by password only.)

www.Truthout.org

Evidence of poison

Fiona Macleod
08 March 2007 11:59

A Limpopo medical doctor has documented a string of physical abnormalities — including
breasts on a five-year-old girl — that he believes are directly linked to the unregulated
use of agricultural chemicals.

Dr Johan Minnaar (44) has produced evidence of serious illnesses and disorders among his
patients in Groblersdal, where commercial farmers are spraying large amounts of
pesticides on crops.

Horrific cases include teenage boys temporarily “growing breasts” during spraying
seasons, miscarriages, partial facial paralysis, cancers and ear malfunctions. Many of his
patients suffer from milder poisoning symptoms, such as asthma, sinusitis, headaches,
dizziness and depression.

Minnaar, who has been practising as a doctor in Groblersdal since 1997, took the unusual
step of coming forward with his evidence after unsuccessful attempts to get government
and regulatory authorities to intervene.

He said: “Groblersdal is surrounded by farms growing mostly citrus and grapes, but also
cotton, vegetables and maize. Throughout the year there is constant crop spraying with
pesticides containing organophosphates and carbamates. No one has informed the
community what pesticides are being used, even though the law states people must be
notified before spraying.”

Minnaar started investigating after realising that symptoms he had experienced over six
years followed a pattern.

“I experienced chronic fatigue, nausea, muscle aches and pains, skin rashes and arthritis,
particularly from August till November, when there is a noticeable increase in the spraying.
On investigation, it became clear that other people had these symptoms at the same time.”

Last August, he became so ill that he had to stay at home for two weeks. His wife and
three children also showed symptoms. He began regularly testing his and his spouse’s
blood and the tests showed they were exposed to organophosphates and carbamate
pesticides.

Minnaar laid complaints with the registrar of the national agriculture department, the
water affairs department and the labour and health departments of the Limpopo
government. He also tackled the farmers, chemical companies and crop sprayers.

The spraying continued and, on two days in February this year, large amounts of
carbamate were released during the aerial spraying of citrus orchards. Residents were not
warned beforehand. Among those who later showed signs of poisoning were pupils of two
schools located in the orchards.

Minnaar said pupils regularly played on the sports fields during spraying. The teenage
boys who had consulted him about “growing breasts” in the spraying seasons attended the
schools.

In late January, a woman brought a five-year-old girl who had developed breasts to his
consulting rooms. Minnaar suspected it could be linked to poisoning and referred her case
to Limpopo government officials, who he met two days later.

“As with many patients, she had no access to medical facilities or funds. The authorities
undertook to get her medical testing and treatment, but we’ve heard nothing,” he said.

According to Professor Leslie London of the University of Cape Town’s health sciences
faculty, premature puberty and other hormonal abnormalities are symptoms of
contamination by pesticides containing “endocrine disruptors”.

A 2005 study of girls in Mexican farming areas, titled Altered Breast Development in Girls,
indicated that pesticides could affect breast development and lead to early puberty.

Said London: “It has been shown that endocrine disruptors can also affect sexual
maturation and differentiation. A study in Sri Lanka of a pesticide called endosulfan found
that boys living in villages below cashew nut plantations sprayed with endosulfan had
impaired sexual maturity and other reproductive impairments.”

London researched aerial crop spraying around Groblersdal in 2005, with a focus on risks
to small farmers rather than health impacts. Last year, he published research on possible
links between aerial organophosphate spraying in the Northern Cape and Guillain-Barré
Syndrome, a neurological disorder.

“The problem of rural towns affected by agricultural application of pesticides is
ubiquitous,” he said. “Present regulatory and safety management methods really don’t
address this problem sufficiently.

“I think there is a view that if you choose to live in the country, you should accept this as a
way of life. That is a societal value decision, not a matter of science.”

The health department’s directorate of environmental health has announced plans to
launch a chemical safety programme in Groblersdal at the end of March. According to its
draft concept document, “the aim is to launch the programme to inform provinces that
national [government] is willing to assist them in the management of chemicals”.

The draft programme identifies schoolchildren, women, farmers and farmworkers, shack
dwellers, informal traders and manufacturers as the “most vulnerable communities in
municipalities that lack capacity to properly and satisfactorily deal with chemical safety
issues”.

South Africa is a signatory to international conventions aimed at promoting chemical
safety, and the labour ministry said in October that chemical safety was “high on the
minister’s agenda”. But crop spraying is a highly technical industry, and pinpointing
contamination is difficult.

London said it was almost impossible for applicators in planes to control the drift of
chemical sprays. “Aerial application has been shown in some studies to drift more than
2km, even in the absence of strong winds.”

European countries strictly regulate the industry through buffer zones around residential
areas and warning systems, he added.

Gerrit van Vuuren, an aerial application consultant at Croplife South Africa, blamed mist-
spraying of crops on the ground. “It is absolutely wrong to conclude that because there is
a yellow aircraft spraying agrichemicals in an area, it must the reason for ill health effects,”
he said.

Van Vuuren said mist-blowers apply more than 1 000 litres of spray mixture a hectare,
compared to 30 to 40 litres in the case of aerial spraying. They also blow a significant
volume of the spray higher than 6m into the air.

“A couple of mist-blowers spraying thousands of litres of spray mixtures at night are less
visible than an aircraft spraying a couple of hundred litres in the morning.”

He said it was up to farmers to notify inhabitants and issue warnings. They were also
supposed to ensure no one entered their fields during spraying.

The environmental health unit at the Elias Motsoaledi municipality, under which
Groblersdal falls, said it was “busy investigating the usage of pesticides being sprayed
from aeroplanes, as nuisances do occur from these activities”.

But Minnaar is frustrated by government promises to investigate. “For all practical
purposes, the supposed controls are not working. While they keep promising to sort it out,
we are getting poisoned,” he said.

Categories : Activism, Blog / Vlog, CODEX Consequences, Compulsory Drugging, Disinformation, Medical Hazards, Organics
Tags : Compusory Drugging, Contamination, Environmental toxins, EPA, FDA, health freedom, MSG, Natural Solutions Foundation, NSF, toxins, USDA

Farmer In Chief: Health Freedom, Food Policy and the Elections

By Administrator on October 23, 2008 No Comments

The Natural Solutions Foundation has been urging the US to examine its food policies in favor of clean, unadulterated, locally grown, GMO free foods for years. We have asked supporters to write letters, met with senior Congressional Aides and members of Congress, attended Codex meetings where FDA and USDA representatives foster the worst of the worst of the multinational interests with respect to adulterated food and enhanced profits.

All along, we have been educating our supporters, who number in the hundreds of thousands, and others as well, to understand that the economic, social, personal and national impact of a degraded food system is the destruction not only of the individual, but the entire society.

If people are dying or dead, or caring for the ill, they cannot go to school, work or carry out the essential functions of a society. If 16% of the GNP goes, at it does in America, for health care that does not care about health, but profits only from illness, and food, the only source of nutrition and health, is contaminated for the sake of profit, and at the same time that nation has just about the worst health of any developed nation, despite all the wildly expensive “care” something is rotten in Denmark, or, rather, the US. And what is rotten is our food.

Our chemicalized, synthesized, devitalized, devalued and destroyed food is, in fact, what is wrong. Without nutrition the immune system flags and falters. Without nutrition, the brain does not function well, Without nutrition the reproductive systems grinds to a halt.

Without nutrition, the eyes grow dim. Obvious but true: synthetic food does not provide nutitional sufficiency. Food that is transported a half a world away looses its nutritional value.

People who eat food made from GMOs ingest, incorporate and keep within them the seeds of their own destruction and that of any child they might bear.

Science is clear. But profit is, apparently, clearer.

Cheap food is not good food. Cheap food is expensive social degreedation and expensive disease. Very, very expensive disease.

And that is, perhaps a good point to remember: Back in 1952 the head of Germany’s Bayer Pharmaceutical, Fritz ter Meer, brought a letter to the UN signed by 5 pharmaceutical executives who haD, like ter Meer, all gone to prison at the end of the Second World War for crimes against humanity and who were now, once again, working for pharmaceutical firms.

Chief executives (and, in ter Meer’s case, the head) of the great civilian German war machine “I G Farben”, these pharmaceutical executives knew well that to accomplish the dream of world domination and cleansing which the Third Reich’s fall left unfinished, they would need to control – and kill – much of the world’s population.

What better way than food? So they urged the UN, in their letter, to take control of the world’s food. He who controls the world’s food, after all, controls the world. And pharmaceutical executives, whose legal responsibility to their share holders have, after all, no interest at all in healthy food. Healthy food makes healthy people and they are poor customers for the diseases which fuel the astronomical profits of the pharmaceutical industry – the preventable, non communicable diseases of under nutrition, as the World Health Organization calls them. These diseases kill an increasing portion of the world’s people as the world converts to Codex-compliant, USDA and FDA approved “food” which weakens and sickens us individually and in our body politic.

It is the drug lord’s gambit, now writ large through the participation of the biotech industry, the factory farming industry, the pesticide industry, the veterinary drug industry (Big Pharma again, because more drugs are used annually for animals than for people), the irradiation industry and the Chemical industry. Codex is part of the picture. Codex was born from that impulse.

Visit Nutricide, http://video.google.com/videoplay?docid=-5266884912495233634 to learn more about the origins and impact of Codex Alimentarius (the World Food Code) on your health and the world’s.

Please read below this posting for more information on how to take back the world’s food production, put it back in the capable hands of farmers and reverse the devastating nutrition-based illness trends which will be responsible for 75 % of the world’s people by 2025, according to the joint publication of the World Health Organization and the Food and Agriculture Organization’s,

    The Role of Diet and Exercise in the Prevention of Chronic Disease

visit www.NaturalSolutionsFoundation.org to learn about the Natural Solutions Foundation’s International Decade of Nutrition and its Valley of the Moon(TM) Eco Demonstration Community in the highlands of Panama’s Chiriqui Highlands.

WHO/FAO’s joint report on the impact of the PREVENTABLE, non communicable chronic degenerative diseases of under nutrition “It has been projected that, by 2020, chronic diseases will account for
almost three-quarters of all deaths worldwide, and that 71% of deaths due to ischaemic heart disease (IHD), 75% of deaths due to stroke, and 70% of deaths due to diabetes will occur in developing countries (4). The number of people in the developing world with diabetes will increase by more than 2.5-fold, from 84 million in 1995 to 228 million in 2025 (5). On a global basis, 60% of the burden of chronic diseases will occur in developing countries.” reaching the proportions already attained in the developed world for these diseases of under nutrition.

Then National Solutions Foundation strongly supports taking back the production of food from the multinational corporations who are, literally, killing us and putting it back into the hands and lands of people who know, and love, the food they grow and are part of the communities they serve. That’s what the International Decade of Nutrition is all about and that is the reason that the Valley of the Moon(TM) Eco Community will house not only a BeyondOrganic(TM) Bio Dynamic Zero Emissions Farm, but a farm school as well.

Please give generously to the Natural Solutions Foundation health freedom and International Decade of Nutrition activities. Click here (http://drrimatruthreports.com/index.php?page_id=189) to make your tax deductible recurring donation.

And click here (http://drrimatruthreports.com/?page_id=1130) to purchase chemical free Valley of the Moon(TM) Chemical Free Coffee, A little bit of heaven in a cup(c). Every bag gives you a 1/2 lb of the world’s best chemical free coffee and gives you a tax deduction, too!

Thanks for your support.
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
www.NaturalSolutionsFoundation.org
www.Organics4U.org
www.NaturalSolutionsMarketPlace.org
www.NaturalSolutionsMedia.tv

Farmer in Chief
Michael Pollan, The New York Times
Thursday 09 October 2008
(Copyright – New York Times)

[Reproduced for Educational purposes.]

Federal policies to promote maximum production of commodity crops such as wheat, from which most of our supermarket foods are derived, have succeeded in keeping prices low. But suddenly the era of cheap and abundant food appears to be drawing to a close.

Dear Mr. President-Elect,

It may surprise you to learn that among the issues that will occupy much of your time in the coming years is one you barely mentioned during the campaign: food. Food policy is not something American presidents have had to give much thought to, at least since the Nixon administration – the last time high food prices presented a serious political peril. Since then, federal policies to promote maximum production of the commodity crops (corn, soybeans, wheat and rice) from which most of our supermarket foods are derived have succeeded impressively in keeping prices low and food more or less off the national political agenda. But with a suddenness that has taken us all by surprise, the era of cheap and abundant food appears to be drawing to a close. What this means is that you, like so many other leaders through history, will find yourself confronting the fact – so easy to overlook these past few years – that the health of a nation’s food system is a critical issue of national security. Food is about to demand your attention.

Complicating matters is the fact that the price and abundance of food are not the only problems we face; if they were, you could simply follow Nixon’s example, appoint a latter-day Earl Butz as your secretary of agriculture and instruct him or her to do whatever it takes to boost production. But there are reasons to think that the old approach won’t work this time around; for one thing, it depends on cheap energy that we can no longer count on. For another, expanding production of industrial agriculture today would require you to sacrifice important values on which you did campaign. Which brings me to the deeper reason you will need not simply to address food prices but to make the reform of the entire food system one of the highest priorities of your administration: unless you do, you will not be able to make significant progress on the health care crisis, energy independence or climate change. Unlike food, these are issues you did campaign on – but as you try to address them you will quickly discover that the way we currently grow, process and eat food in America goes to the heart of all three problems and will have to change if we hope to solve them. Let me explain.

After cars, the food system uses more fossil fuel than any other sector of the economy – 19 percent. And while the experts disagree about the exact amount, the way we feed ourselves contributes more greenhouse gases to the atmosphere than anything else we do – as much as 37 percent, according to one study. Whenever farmers clear land for crops and till the soil, large quantities of carbon are released into the air. But the 20th-century industrialization of agriculture has increased the amount of greenhouse gases emitted by the food system by an order of magnitude; chemical fertilizers (made from natural gas), pesticides (made from petroleum), farm machinery, modern food processing and packaging and transportation have together transformed a system that in 1940 produced 2.3 calories of food energy for every calorie of fossil-fuel energy it used into one that now takes 10 calories of fossil-fuel energy to produce a single calorie of modern supermarket food. Put another way, when we eat from the industrial-food system, we are eating oil and spewing greenhouse gases. This state of affairs appears all the more absurd when you recall that every calorie we eat is ultimately the product of photosynthesis – a process based on making food energy from sunshine. There is hope and possibility in that simple fact.

In addition to the problems of climate change and America’s oil addiction, you have spoken at length on the campaign trail of the health care crisis. Spending on health care has risen from 5 percent of national income in 1960 to 16 percent today, putting a significant drag on the economy. The goal of ensuring the health of all Americans depends on getting those costs under control. There are several reasons health care has gotten so expensive, but one of the biggest, and perhaps most tractable, is the cost to the system of preventable chronic diseases. Four of the top 10 killers in America today are chronic diseases linked to diet: heart disease, stroke, Type 2 diabetes and cancer. It is no coincidence that in the years national spending on health care went from 5 percent to 16 percent of national income, spending on food has fallen by a comparable amount – from 18 percent of household income to less than 10 percent. While the surfeit of cheap calories that the U.S. food system has produced since the late 1970s may have taken food prices off the political agenda, this has come at a steep cost to public health. You cannot expect to reform the health care system, much less expand coverage, without confronting the public-health catastrophe that is the modern American diet.

The impact of the American food system on the rest of the world will have implications for your foreign and trade policies as well. In the past several months more than 30 nations have experienced food riots, and so far one government has fallen. Should high grain prices persist and shortages develop, you can expect to see the pendulum shift decisively away from free trade, at least in food. Nations that opened their markets to the global flood of cheap grain (under pressure from previous administrations as well as the World Bank and the I.M.F.) lost so many farmers that they now find their ability to feed their own populations hinges on decisions made in Washington (like your predecessor’s precipitous embrace of biofuels) and on Wall Street. They will now rush to rebuild their own agricultural sectors and then seek to protect them by erecting trade barriers. Expect to hear the phrases “food sovereignty” and “food security” on the lips of every foreign leader you meet. Not only the Doha round, but the whole cause of free trade in agriculture is probably dead, the casualty of a cheap food policy that a scant two years ago seemed like a boon for everyone. It is one of the larger paradoxes of our time that the very same food policies that have contributed to overnutrition in the first world are now contributing to undernutrition in the third. But it turns out that too much food can be nearly as big a problem as too little – a lesson we should keep in mind as we set about designing a new approach to food policy.

Rich or poor, countries struggling with soaring food prices are being forcibly reminded that food is a national-security issue. When a nation loses the ability to substantially feed itself, it is not only at the mercy of global commodity markets but of other governments as well. At issue is not only the availability of food, which may be held hostage by a hostile state, but its safety: as recent scandals in China demonstrate, we have little control over the safety of imported foods. The deliberate contamination of our food presents another national-security threat. At his valedictory press conference in 2004, Tommy Thompson, the secretary of health and human services, offered a chilling warning, saying, “I, for the life of me, cannot understand why the terrorists have not attacked our food supply, because it is so easy to do.”

This, in brief, is the bad news: the food and agriculture policies you’ve inherited – designed to maximize production at all costs and relying on cheap energy to do so – are in shambles, and the need to address the problems they have caused is acute. The good news is that the twinned crises in food and energy are creating a political environment in which real reform of the food system may actually be possible for the first time in a generation. The American people are paying more attention to food today than they have in decades, worrying not only about its price but about its safety, its provenance and its healthfulness. There is a gathering sense among the public that the industrial-food system is broken. Markets for alternative kinds of food – organic, local, pasture-based, humane – are thriving as never before. All this suggests that a political constituency for change is building and not only on the left: lately, conservative voices have also been raised in support of reform. Writing of the movement back to local food economies, traditional foods (and family meals) and more sustainable farming, The American Conservative magazine editorialized last summer that “this is a conservative cause if ever there was one.”

There are many moving parts to the new food agenda I’m urging you to adopt, but the core idea could not be simpler: we need to wean the American food system off its heavy 20th-century diet of fossil fuel and put it back on a diet of contemporary sunshine. True, this is easier said than done – fossil fuel is deeply implicated in everything about the way we currently grow food and feed ourselves. To put the food system back on sunlight will require policies to change how things work at every link in the food chain: in the farm field, in the way food is processed and sold and even in the American kitchen and at the American dinner table. Yet the sun still shines down on our land every day, and photosynthesis can still work its wonders wherever it does. If any part of the modern economy can be freed from its dependence on oil and successfully resolarized, surely it is food.

How We Got Here

Before setting out an agenda for reforming the food system, it’s important to understand how that system came to be – and also to appreciate what, for all its many problems, it has accomplished. What our food system does well is precisely what it was designed to do, which is to produce cheap calories in great abundance. It is no small thing for an American to be able to go into a fast-food restaurant and to buy a double cheeseburger, fries and a large Coke for a price equal to less than an hour of labor at the minimum wage – indeed, in the long sweep of history, this represents a remarkable achievement.

It must be recognized that the current food system – characterized by monocultures of corn and soy in the field and cheap calories of fat, sugar and feedlot meat on the table – is not simply the product of the free market. Rather, it is the product of a specific set of government policies that sponsored a shift from solar (and human) energy on the farm to fossil-fuel energy.

Did you notice when you flew over Iowa during the campaign how the land was completely bare – black – from October to April? What you were seeing is the agricultural landscape created by cheap oil. In years past, except in the dead of winter, you would have seen in those fields a checkerboard of different greens: pastures and hayfields for animals, cover crops, perhaps a block of fruit trees. Before the application of oil and natural gas to agriculture, farmers relied on crop diversity (and photosynthesis) both to replenish their soil and to combat pests, as well as to feed themselves and their neighbors. Cheap energy, however, enabled the creation of monocultures, and monocultures in turn vastly increased the productivity both of the American land and the American farmer; today the typical corn-belt farmer is single-handedly feeding 140 people.

This did not occur by happenstance. After World War II, the government encouraged the conversion of the munitions industry to fertilizer – ammonium nitrate being the main ingredient of both bombs and chemical fertilizer – and the conversion of nerve-gas research to pesticides. The government also began subsidizing commodity crops, paying farmers by the bushel for all the corn, soybeans, wheat and rice they could produce. One secretary of agriculture after another implored them to plant “fence row to fence row” and to “get big or get out.”

The chief result, especially after the Earl Butz years, was a flood of cheap grain that could be sold for substantially less than it cost farmers to grow because a government check helped make up the difference. As this artificially cheap grain worked its way up the food chain, it drove down the price of all the calories derived from that grain: the high-fructose corn syrup in the Coke, the soy oil in which the potatoes were fried, the meat and cheese in the burger.

Subsidized monocultures of grain also led directly to monocultures of animals: since factory farms could buy grain for less than it cost farmers to grow it, they could now fatten animals more cheaply than farmers could. So America’s meat and dairy animals migrated from farm to feedlot, driving down the price of animal protein to the point where an American can enjoy eating, on average, 190 pounds of meat a year – a half pound every day.

But if taking the animals off farms made a certain kind of economic sense, it made no ecological sense whatever: their waste, formerly regarded as a precious source of fertility on the farm, became a pollutant – factory farms are now one of America’s biggest sources of pollution. As Wendell Berry has tartly observed, to take animals off farms and put them on feedlots is to take an elegant solution – animals replenishing the fertility that crops deplete – and neatly divide it into two problems: a fertility problem on the farm and a pollution problem on the feedlot. The former problem is remedied with fossil-fuel fertilizer; the latter is remedied not at all.

What was once a regional food economy is now national and increasingly global in scope – thanks again to fossil fuel. Cheap energy – for trucking food as well as pumping water – is the reason New York City now gets its produce from California rather than from the “Garden State” next door, as it did before the advent of Interstate highways and national trucking networks. More recently, cheap energy has underwritten a globalized food economy in which it makes (or rather, made) economic sense to catch salmon in Alaska, ship it to China to be filleted and then ship the fillets back to California to be eaten; or one in which California and Mexico can profitably swap tomatoes back and forth across the border; or Denmark and the United States can trade sugar cookies across the Atlantic. About that particular swap the economist Herman Daly once quipped, “Exchanging recipes would surely be more efficient.”

Whatever we may have liked about the era of cheap, oil-based food, it is drawing to a close. Even if we were willing to continue paying the environmental or public-health price, we’re not going to have the cheap energy (or the water) needed to keep the system going, much less expand production. But as is so often the case, a crisis provides opportunity for reform, and the current food crisis presents opportunities that must be seized.

In drafting these proposals, I’ve adhered to a few simple principles of what a 21st-century food system needs to do. First, your administration’s food policy must strive to provide a healthful diet for all our people; this means focusing on the quality and diversity (and not merely the quantity) of the calories that American agriculture produces and American eaters consume. Second, your policies should aim to improve the resilience, safety and security of our food supply. Among other things, this means promoting regional food economies both in America and around the world. And lastly, your policies need to reconceive agriculture as part of the solution to environmental problems like climate change.

These goals are admittedly ambitious, yet they will not be difficult to align or advance as long as we keep in mind this One Big Idea: most of the problems our food system faces today are because of its reliance on fossil fuels, and to the extent that our policies wring the oil out of the system and replace it with the energy of the sun, those policies will simultaneously improve the state of our health, our environment and our security.

I. Resolarizing the American Farm

What happens in the field influences every other link of the food chain on up to our meals – if we grow monocultures of corn and soy, we will find the products of processed corn and soy on our plates. Fortunately for your initiative, the federal government has enormous leverage in determining exactly what happens on the 830 million acres of American crop and pasture land.

Today most government farm and food programs are designed to prop up the old system of maximizing production from a handful of subsidized commodity crops grown in monocultures. Even food-assistance programs like WIC and school lunch focus on maximizing quantity rather than quality, typically specifying a minimum number of calories (rather than maximums) and seldom paying more than lip service to nutritional quality. This focus on quantity may have made sense in a time of food scarcity, but today it gives us a school-lunch program that feeds chicken nuggets and Tater Tots to overweight and diabetic children.

Your challenge is to take control of this vast federal machinery and use it to drive a transition to a new solar-food economy, starting on the farm. Right now, the government actively discourages the farmers it subsidizes from growing healthful, fresh food: farmers receiving crop subsidies are prohibited from growing “specialty crops” – farm-bill speak for fruits and vegetables. (This rule was the price exacted by California and Florida produce growers in exchange for going along with subsidies for commodity crops.) Commodity farmers should instead be encouraged to grow as many different crops – including animals – as possible. Why? Because the greater the diversity of crops on a farm, the less the need for both fertilizers and pesticides.

The power of cleverly designed polycultures to produce large amounts of food from little more than soil, water and sunlight has been proved, not only by small-scale “alternative” farmers in the United States but also by large rice-and-fish farmers in China and giant-scale operations (up to 15,000 acres) in places like Argentina. There, in a geography roughly comparable to that of the American farm belt, farmers have traditionally employed an ingenious eight-year rotation of perennial pasture and annual crops: after five years grazing cattle on pasture (and producing the world’s best beef), farmers can then grow three years of grain without applying any fossil-fuel fertilizer. Or, for that matter, many pesticides: the weeds that afflict pasture can’t survive the years of tillage, and the weeds of row crops don’t survive the years of grazing, making herbicides all but unnecessary. There is no reason – save current policy and custom – that American farmers couldn’t grow both high-quality grain and grass-fed beef under such a regime through much of the Midwest. (It should be noted that today’s sky-high grain prices are causing many Argentine farmers to abandon their rotation to grow grain and soybeans exclusively, an environmental disaster in the making.)

Federal policies could do much to encourage this sort of diversified sun farming. Begin with the subsidies: payment levels should reflect the number of different crops farmers grow or the number of days of the year their fields are green – that is, taking advantage of photosynthesis, whether to grow food, replenish the soil or control erosion. If Midwestern farmers simply planted a cover crop after the fall harvest, they would significantly reduce their need for fertilizer, while cutting down on soil erosion. Why don’t farmers do this routinely? Because in recent years fossil-fuel-based fertility has been so much cheaper and easier to use than sun-based fertility.

In addition to rewarding farmers for planting cover crops, we should make it easier for them to apply compost to their fields – a practice that improves not only the fertility of the soil but also its ability to hold water and therefore withstand drought. (There is mounting evidence that it also boosts the nutritional quality of the food grown in it.) The U.S.D.A. estimates that Americans throw out 14 percent of the food they buy; much more is wasted by retailers, wholesalers and institutions. A program to make municipal composting of food and yard waste mandatory and then distributing the compost free to area farmers would shrink America’s garbage heap, cut the need for irrigation and fossil-fuel fertilizers in agriculture and improve the nutritional quality of the American diet.

Right now, most of the conservation programs run by the U.S.D.A. are designed on the zero-sum principle: land is either locked up in “conservation” or it is farmed intensively. This either-or approach reflects an outdated belief that modern farming and ranching are inherently destructive, so that the best thing for the environment is to leave land untouched. But we now know how to grow crops and graze animals in systems that will support biodiversity, soil health, clean water and carbon sequestration. The Conservation Stewardship Program, championed by Senator Tom Harkin and included in the 2008 Farm Bill, takes an important step toward rewarding these kinds of practices, but we need to move this approach from the periphery of our farm policy to the very center. Longer term, the government should back ambitious research now under way (at the Land Institute in Kansas and a handful of other places) to “perennialize” commodity agriculture: to breed varieties of wheat, rice and other staple grains that can be grown like prairie grasses – without having to till the soil every year. These perennial grains hold the promise of slashing the fossil fuel now needed to fertilize and till the soil, while protecting farmland from erosion and sequestering significant amounts of carbon.

But that is probably a 50-year project. For today’s agriculture to wean itself from fossil fuel and make optimal use of sunlight, crop plants and animals must once again be married on the farm – as in Wendell Berry’s elegant “solution.” Sunlight nourishes the grasses and grains, the plants nourish the animals, the animals then nourish the soil, which in turn nourishes the next season’s grasses and grains. Animals on pasture can also harvest their own feed and dispose of their own waste – all without our help or fossil fuel.

If this system is so sensible, you might ask, why did it succumb to Confined Animal Feeding Operations, or CAFOs? In fact there is nothing inherently efficient or economical about raising vast cities of animals in confinement. Three struts, each put into place by federal policy, support the modern CAFO, and the most important of these – the ability to buy grain for less than it costs to grow it – has just been kicked away. The second strut is F.D.A. approval for the routine use of antibiotics in feed, without which the animals in these places could not survive their crowded, filthy and miserable existence. And the third is that the government does not require CAFOs to treat their wastes as it would require human cities of comparable size to do. The F.D.A. should ban the routine use of antibiotics in livestock feed on public-health grounds, now that we have evidence that the practice is leading to the evolution of drug-resistant bacterial diseases and to outbreaks of E. coli and salmonella poisoning. CAFOs should also be regulated like the factories they are, required to clean up their waste like any other industry or municipality.

It will be argued that moving animals off feedlots and back onto farms will raise the price of meat. It probably will – as it should. You will need to make the case that paying the real cost of meat, and therefore eating less of it, is a good thing for our health, for the environment, for our dwindling reserves of fresh water and for the welfare of the animals. Meat and milk production represent the food industry’s greatest burden on the environment; a recent U.N. study estimated that the world’s livestock alone account for 18 percent of all greenhouse gases, more than all forms of transportation combined. (According to one study, a pound of feedlot beef also takes 5,000 gallons of water to produce.) And while animals living on farms will still emit their share of greenhouse gases, grazing them on grass and returning their waste to the soil will substantially offset their carbon hoof prints, as will getting ruminant animals off grain. A bushel of grain takes approximately a half gallon of oil to produce; grass can be grown with little more than sunshine.

It will be argued that sun-food agriculture will generally yield less food than fossil-fuel agriculture. This is debatable. The key question you must be prepared to answer is simply this: Can the sort of sustainable agriculture you’re proposing feed the world?

There are a couple of ways to answer this question. The simplest and most honest answer is that we don’t know, because we haven’t tried. But in the same way we now need to learn how to run an industrial economy without cheap fossil fuel, we have no choice but to find out whether sustainable agriculture can produce enough food. The fact is, during the past century, our agricultural research has been directed toward the goal of maximizing production with the help of fossil fuel. There is no reason to think that bringing the same sort of resources to the development of more complex, sun-based agricultural systems wouldn’t produce comparable yields. Today’s organic farmers, operating for the most part without benefit of public investment in research, routinely achieve 80 to 100 percent of conventional yields in grain and, in drought years, frequently exceed conventional yields. (This is because organic soils better retain moisture.) Assuming no further improvement, could the world – with a population expected to peak at 10 billion – survive on these yields?

First, bear in mind that the average yield of world agriculture today is substantially lower than that of modern sustainable farming. According to a recent University of Michigan study, merely bringing international yields up to today’s organic levels could increase the world’s food supply by 50 percent.

The second point to bear in mind is that yield isn’t everything – and growing high-yield commodities is not quite the same thing as growing food. Much of what we’re growing today is not directly eaten as food but processed into low-quality calories of fat and sugar. As the world epidemic of diet-related chronic disease has demonstrated, the sheer quantity of calories that a food system produces improves health only up to a point, but after that, quality and diversity are probably more important. We can expect that a food system that produces somewhat less food but of a higher quality will produce healthier populations.

The final point to consider is that 40 percent of the world’s grain output today is fed to animals; 11 percent of the world’s corn and soybean crop is fed to cars and trucks, in the form of biofuels. Provided the developed world can cut its consumption of grain-based animal protein and ethanol, there should be plenty of food for everyone – however we choose to grow it.

In fact, well-designed polyculture systems, incorporating not just grains but vegetables and animals, can produce more food per acre than conventional monocultures, and food of a much higher nutritional value. But this kind of farming is complicated and needs many more hands on the land to make it work. Farming without fossil fuels – performing complex rotations of plants and animals and managing pests without petrochemicals – is labor intensive and takes more skill than merely “driving and spraying,” which is how corn-belt farmers describe what they do for a living.

To grow sufficient amounts of food using sunlight will require more people growing food – millions more. This suggests that sustainable agriculture will be easier to implement in the developing world, where large rural populations remain, than in the West, where they don’t. But what about here in America, where we have only about two million farmers left to feed a population of 300 million? And where farmland is being lost to development at the rate of 2,880 acres a day? Post-oil agriculture will need a lot more people engaged in food production – as farmers and probably also as gardeners.

The sun-food agenda must include programs to train a new generation of farmers and then help put them on the land. The average American farmer today is 55 years old; we shouldn’t expect these farmers to embrace the sort of complex ecological approach to agriculture that is called for. Our focus should be on teaching ecological farming systems to students entering land-grant colleges today. For decades now, it has been federal policy to shrink the number of farmers in America by promoting capital-intensive monoculture and consolidation. As a society, we devalued farming as an occupation and encouraged the best students to leave the farm for “better” jobs in the city. We emptied America’s rural counties in order to supply workers to urban factories. To put it bluntly, we now need to reverse course. We need more highly skilled small farmers in more places all across America – not as a matter of nostalgia for the agrarian past but as a matter of national security. For nations that lose the ability to substantially feed themselves will find themselves as gravely compromised in their international dealings as nations that depend on foreign sources of oil presently do. But while there are alternatives to oil, there are no alternatives to food.

National security also argues for preserving every acre of farmland we can and then making it available to new farmers. We simply will not be able to depend on distant sources of food, and therefore need to preserve every acre of good farmland within a day’s drive of our cities. In the same way that when we came to recognize the supreme ecological value of wetlands we erected high bars to their development, we need to recognize the value of farmland to our national security and require real-estate developers to do “food-system impact statements” before development begins. We should also create tax and zoning incentives for developers to incorporate farmland (as they now do “open space”) in their subdivision plans; all those subdivisions now ringing golf courses could someday have diversified farms at their center.

The revival of farming in America, which of course draws on the abiding cultural power of our agrarian heritage, will pay many political and economic dividends. It will lead to robust economic renewal in the countryside. And it will generate tens of millions of new “green jobs,” which is precisely how we need to begin thinking of skilled solar farming: as a vital sector of the 21st-century post-fossil-fuel economy.

II. Reregionalizing the Food System

For your sun-food agenda to succeed, it will have to do a lot more than alter what happens on the farm. The government could help seed a thousand new polyculture farmers in every county in Iowa, but they would promptly fail if the grain elevator remained the only buyer in town and corn and beans were the only crops it would take. Resolarizing the food system means building the infrastructure for a regional food economy – one that can support diversified farming and, by shortening the food chain, reduce the amount of fossil fuel in the American diet.

A decentralized food system offers a great many other benefits as well. Food eaten closer to where it is grown will be fresher and require less processing, making it more nutritious. Whatever may be lost in efficiency by localizing food production is gained in resilience: regional food systems can better withstand all kinds of shocks. When a single factory is grinding 20 million hamburger patties in a week or washing 25 million servings of salad, a single terrorist armed with a canister of toxins can, at a stroke, poison millions. Such a system is equally susceptible to accidental contamination: the bigger and more global the trade in food, the more vulnerable the system is to catastrophe. The best way to protect our food system against such threats is obvious: decentralize it.

Today in America there is soaring demand for local and regional food; farmers’ markets, of which the U.S.D.A. estimates there are now 4,700, have become one of the fastest-growing segments of the food market. Community-supported agriculture is booming as well: there are now nearly 1,500 community-supported farms, to which consumers pay an annual fee in exchange for a weekly box of produce through the season. The local-food movement will continue to grow with no help from the government, especially as high fuel prices make distant and out-of-season food, as well as feedlot meat, more expensive. Yet there are several steps the government can take to nurture this market and make local foods more affordable. Here are a few:

Four-Season Farmers’ Markets. Provide grants to towns and cities to build year-round indoor farmers’ markets, on the model of Pike Place in Seattle or the Reading Terminal Market in Philadelphia. To supply these markets, the U.S.D.A. should make grants to rebuild local distribution networks in order to minimize the amount of energy used to move produce within local food sheds.

Agricultural Enterprise Zones. Today the revival of local food economies is being hobbled by a tangle of regulations originally designed to check abuses by the very largest food producers. Farmers should be able to smoke a ham and sell it to their neighbors without making a huge investment in federally approved facilities. Food-safety regulations must be made sensitive to scale and marketplace, so that a small producer selling direct off the farm or at a farmers’ market is not regulated as onerously as a multinational food manufacturer. This is not because local food won’t ever have food-safety problems – it will – only that its problems will be less catastrophic and easier to manage because local food is inherently more traceable and accountable.

Local Meat-Inspection Corps. Perhaps the single greatest impediment to the return of livestock to the land and the revival of local, grass-based meat production is the disappearance of regional slaughter facilities. The big meat processors have been buying up local abattoirs only to close them down as they consolidate, and the U.S.D.A. does little to support the ones that remain. From the department’s perspective, it is a better use of shrinking resources to dispatch its inspectors to a plant slaughtering 400 head an hour than to a regional abattoir slaughtering a dozen. The U.S.D.A. should establish a Local Meat-Inspectors Corps to serve these processors. Expanding on its successful pilot program on Lopez Island in Puget Sound, the U.S.D.A. should also introduce a fleet of mobile abattoirs that would go from farm to farm, processing animals humanely and inexpensively. Nothing would do more to make regional, grass-fed meat fully competitive in the market with feedlot meat.

Establish a Strategic Grain Reserve. In the same way the shift to alternative energy depends on keeping oil prices relatively stable, the sun-food agenda – as well as the food security of billions of people around the world – will benefit from government action to prevent huge swings in commodity prices. A strategic grain reserve, modeled on the Strategic Petroleum Reserve, would help achieve this objective and at the same time provide some cushion for world food stocks, which today stand at perilously low levels. Governments should buy and store grain when it is cheap and sell when it is dear, thereby moderating price swings in both directions and discouraging speculation.

Regionalize Federal Food Procurement. In the same way that federal procurement is often used to advance important social goals (like promoting minority-owned businesses), we should require that some minimum percentage of government food purchases – whether for school-lunch programs, military bases or federal prisons – go to producers located within 100 miles of institutions buying the food. We should create incentives for hospitals and universities receiving federal funds to buy fresh local produce. To channel even a small portion of institutional food purchasing to local food would vastly expand regional agriculture and improve the diet of the millions of people these institutions feed.

Create a Federal Definition of “Food.” It makes no sense for government food-assistance dollars, intended to improve the nutritional health of at-risk Americans, to support the consumption of products we know to be unhealthful. Yes, some people will object that for the government to specify what food stamps can and cannot buy smacks of paternalism. Yet we already prohibit the purchase of tobacco and alcohol with food stamps. So why not prohibit something like soda, which is arguably less nutritious than red wine? Because it is, nominally, a food, albeit a “junk food.” We need to stop flattering nutritionally worthless foodlike substances by calling them “junk food” – and instead make clear that such products are not in fact food of any kind. Defining what constitutes real food worthy of federal support will no doubt be controversial (you’ll recall President Reagan’s ketchup imbroglio), but defining food upward may be more politically palatable than defining it down, as Reagan sought to do. One approach would be to rule that, in order to be regarded as a food by the government, an edible substance must contain a certain minimum ratio of micronutrients per calorie of energy. At a stroke, such a definition would improve the quality of school lunch and discourage sales of unhealthful products, since typically only “food” is exempt from local sales tax.

A few other ideas: Food-stamp debit cards should double in value whenever swiped at a farmers’ markets – all of which, by the way, need to be equipped with the Electronic Benefit Transfer card readers that supermarkets already have. We should expand the WIC program that gives farmers’-market vouchers to low-income women with children; such programs help attract farmers’ markets to urban neighborhoods where access to fresh produce is often nonexistent. (We should also offer tax incentives to grocery chains willing to build supermarkets in underserved neighborhoods.) Federal food assistance for the elderly should build on a successful program pioneered by the state of Maine that buys low-income seniors a membership in a community-supported farm. All these initiatives have the virtue of advancing two objectives at once: supporting the health of at-risk Americans and the revival of local food economies.

III. Rebuilding America’s Food Culture

In the end, shifting the American diet from a foundation of imported fossil fuel to local sunshine will require changes in our daily lives, which by now are deeply implicated in the economy and culture of fast, cheap and easy food. Making available more healthful and more sustainable food does not guarantee it will be eaten, much less appreciated or enjoyed. We need to use all the tools at our disposal – not just federal policy and public education but the president’s bully pulpit and the example of the first family’s own dinner table – to promote a new culture of food that can undergird your sun-food agenda.

Changing the food culture must begin with our children, and it must begin in the schools. Nearly a half-century ago, President Kennedy announced a national initiative to improve the physical fitness of American children. He did it by elevating the importance of physical education, pressing states to make it a requirement in public schools. We need to bring the same commitment to “edible education” – in Alice Waters’s phrase – by making lunch, in all its dimensions, a mandatory part of the curriculum. On the premise that eating well is a critically important life skill, we need to teach all primary-school students the basics of growing and cooking food and then enjoying it at shared meals.

To change our children’s food culture, we’ll need to plant gardens in every primary school, build fully equipped kitchens, train a new generation of lunchroom ladies (and gentlemen) who can once again cook and teach cooking to children. We should introduce a School Lunch Corps program that forgives federal student loans to culinary-school graduates in exchange for two years of service in the public-school lunch program. And we should immediately increase school-lunch spending per pupil by $1 a day – the minimum amount food-service experts believe it will take to underwrite a shift from fast food in the cafeteria to real food freshly prepared.

But it is not only our children who stand to benefit from public education about food. Today most federal messages about food, from nutrition labeling to the food pyramid, are negotiated with the food industry. The surgeon general should take over from the Department of Agriculture the job of communicating with Americans about their diet. That way we might begin to construct a less equivocal and more effective public-health message about nutrition. Indeed, there is no reason that public-health campaigns about the dangers of obesity and Type 2 diabetes shouldn’t be as tough and as effective as public-health campaigns about the dangers of smoking. The Centers for Disease Control estimates that one in three American children born in 2000 will develop Type 2 diabetes. The public needs to know and see precisely what that sentence means: blindness; amputation; early death. All of which can be avoided by a change in diet and lifestyle. A public-health crisis of this magnitude calls for a blunt public-health message, even at the expense of offending the food industry. Judging by the success of recent antismoking campaigns, the savings to the health care system could be substantial.

There are other kinds of information about food that the government can supply or demand. In general we should push for as much transparency in the food system as possible – the other sense in which “sunlight” should be the watchword of our agenda. The F.D.A. should require that every packaged-food product include a second calorie count, indicating how many calories of fossil fuel went into its production. Oil is one of the most important ingredients in our food, and people ought to know just how much of it they’re eating. The government should also throw its support behind putting a second bar code on all food products that, when scanned either in the store or at home (or with a cellphone), brings up on a screen the whole story and pictures of how that product was produced: in the case of crops, images of the farm and lists of agrochemicals used in its production; in the case of meat and dairy, descriptions of the animals’ diet and drug regimen, as well as live video feeds of the CAFO where they live and, yes, the slaughterhouse where they die. The very length and complexity of the modern food chain breeds a culture of ignorance and indifference among eaters. Shortening the food chain is one way to create more conscious consumers, but deploying technology to pierce the veil is another.

Finally, there is the power of the example you set in the White House. If what’s needed is a change of culture in America’s thinking about food, then how America’s first household organizes its eating will set the national tone, focusing the light of public attention on the issue and communicating a simple set of values that can guide Americans toward sun-based foods and away from eating oil.

The choice of White House chef is always closely watched, and you would be wise to appoint a figure who is identified with the food movement and committed to cooking simply from fresh local ingredients. Besides feeding you and your family exceptionally well, such a chef would demonstrate how it is possible even in Washington to eat locally for much of the year, and that good food needn’t be fussy or complicated but does depend on good farming. You should make a point of the fact that every night you’re in town, you join your family for dinner in the Executive Residence – at a table. (Surely you remember the Reagans’ TV trays.) And you should also let it be known that the White House observes one meatless day a week – a step that, if all Americans followed suit, would be the equivalent, in carbon saved, of taking 20 million midsize sedans off the road for a year. Let the White House chef post daily menus on the Web, listing the farmers who supplied the food, as well as recipes.

Since enhancing the prestige of farming as an occupation is critical to developing the sun-based regional agriculture we need, the White House should appoint, in addition to a White House chef, a White House farmer. This new post would be charged with implementing what could turn out to be your most symbolically resonant step in building a new American food culture. And that is this: tear out five prime south-facing acres of the White House lawn and plant in their place an organic fruit and vegetable garden.

When Eleanor Roosevelt did something similar in 1943, she helped start a Victory Garden movement that ended up making a substantial contribution to feeding the nation in wartime. (Less well known is the fact that Roosevelt planted this garden over the objections of the U.S.D.A., which feared home gardening would hurt the American food industry.) By the end of the war, more than 20 million home gardens were supplying 40 percent of the produce consumed in America. The president should throw his support behind a new Victory Garden movement, this one seeking “victory” over three critical challenges we face today: high food prices, poor diets and a sedentary population. Eating from this, the shortest food chain of all, offers anyone with a patch of land a way to reduce their fossil-fuel consumption and help fight climate change. (We should offer grants to cities to build allotment gardens for people without access to land.) Just as important, Victory Gardens offer a way to enlist

Americans, in body as well as mind, in the work of feeding themselves and changing the food system – something more ennobling, surely, than merely asking them to shop a little differently.

I don’t need to tell you that ripping out even a section of the White House lawn will be controversial: Americans love their lawns, and the South Lawn is one of the most beautiful in the country. But imagine all the energy, water and petrochemicals it takes to make it that way. (Even for the purposes of this memo, the White House would not disclose its lawn-care regimen.) Yet as deeply as Americans feel about their lawns, the agrarian ideal runs deeper still, and making this particular plot of American land productive, especially if the First Family gets out there and pulls weeds now and again, will provide an image even more stirring than that of a pretty lawn: the image of stewardship of the land, of self-reliance and of making the most of local sunlight to feed one’s family and community. The fact that surplus produce from the South Lawn Victory Garden (and there will be literally tons of it) will be offered to regional food banks will make its own eloquent statement.

You’re probably thinking that growing and eating organic food in the White House carries a certain political risk. It is true you might want to plant iceberg lettuce rather than arugula, at least to start. (Or simply call arugula by its proper American name, as generations of Midwesterners have done: “rocket.”) But it should not be difficult to deflect the charge of elitism sometimes leveled at the sustainable-food movement. Reforming the food system is not inherently a right-or-left issue: for every Whole Foods shopper with roots in the counterculture you can find a family of evangelicals intent on taking control of its family dinner and diet back from the fast-food industry – the culinary equivalent of home schooling. You should support hunting as a particularly sustainable way to eat meat – meat grown without any fossil fuels whatsoever. There is also a strong libertarian component to the sun-food agenda, which seeks to free small producers from the burden of government regulation in order to stoke rural innovation. And what is a higher “family value,” after all, than making time to sit down every night to a shared meal?

Our agenda puts the interests of America’s farmers, families and communities ahead of the fast-food industry’s. For that industry and its apologists to imply that it is somehow more “populist” or egalitarian to hand our food dollars to Burger King or General Mills than to support a struggling local farmer is absurd. Yes, sun food costs more, but the reasons why it does only undercut the charge of elitism: cheap food is only cheap because of government handouts and regulatory indulgence (both of which we will end), not to mention the exploitation of workers, animals and the environment on which its putative “economies” depend. Cheap food is food dishonestly priced – it is in fact unconscionably expensive.

Your sun-food agenda promises to win support across the aisle. It builds on America’s agrarian past, but turns it toward a more sustainable, sophisticated future. It honors the work of American farmers and enlists them in three of the 21st century’s most urgent errands: to move into the post-oil era, to improve the health of the American people and to mitigate climate change. Indeed, it enlists all of us in this great cause by turning food consumers into part-time producers, reconnecting the American people with the American land and demonstrating that we need not choose between the welfare of our families and the health of the environment – that eating less oil and more sunlight will redound to the benefit of both.

——-

Michael Pollan, a contributing writer for the magazine, is the Knight Professor of Journalism at the University of California, Berkeley. He is the author, most recently, of “In Defense of Food: An Eater’s Manifesto.”

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Supplements Are “Dangerous” – Poison Press At Work Again

By Administrator on October 14, 2008 No Comments

The Natural Solutions Foundation keeps a close eye on the continuing disinformation of Big Pharma to try to convince you that there is no reason to, or good reason not to, take dietary supplements. It is like Honda telling you that there is no reason to buy, or good reason not to buy, a Toyota.

You see, dietary supplements are the direct economic competitor of drugs. Dietary supplements, like clean, unadulterated food, keep you healthy and get you back to health if you have become ill.

Compared to drugs, they are cheap, safe, easy to use and controllable by you or a helpful nutritionally knowledgeable person. And, at least in the US, they are classified as foods so they cannot be regulated the way drugs would be.

Of course, the FDA is always on the look out to undermine that freedom, recognized by the 1994 Dietary Supplements Health and Education Act (DSHEA) — unanimously adopted by Congress — which this Agency publicly calls “the worst act ever passed by the US Congress”. Why? Because the FDA is run by and for industry and the drug industry is a leading source of FDA funds through User Fees. The big players in the food industry, who pay no user fees to the FDA are, none the less, very important buddies of the organization, so food is regulated for the interests of big industry and drugs are regulated to promote the drug industry, at the expense of anything that might get in the way, like, for example, dietary supplements, or the public good.

Recently pro-industry legislators created an Adverse Event Reporting system for dietary supplements that tries to ignore the role of the many drugs many people use in distorting their metabolism and leading to . Naturally, this created a great PR opportunity to bash and diminish the importance and safety of dietary supplements which do not kill people. Drugs kill people. Foods which are not contaminated do not and dietary supplements are foods!

Dr. Ron Paul, Congressman from Texas, last year called one FDA maneuver an “abuse of power…” and Congress passed dangerous bill under the guidance and force of Senator Ed. Kennedy that further enhanced the power of the FDA. In this case, though, the Health Freedom movement had a partial victory in that we insisted that Congress add a clause to the bill, protecting Dietary Supplements… and Congress, responding to the hundreds of thousands of messages that advocates of health freedom, generated, through our Action Items and otherwise, adopted the protective language.

Yet we recall that genetically modified yeast which produced contaminated Tyrptophane did kill people, giving the FDA the excuse it was seeing to remove this safe and effective sleep and calming amino acid from the market. It was, after all, cutting into the drug market heavily. The FDA did not take genetically modified products off the market. And the company which produced the contaminated shipment in Japan had a sudden and very mysterious fire which destroyed the factory – and any evidence of contamination – almost immediately after the incident was revealed.

Such is the corruption of an agency which regulates both food and drugs. Clearly, those functions must be separated and a new agency which is consumer controlled must be created. Click here () to make sure that happens!

In the meantime, read the important analysis of the latest “Dietary Supplements are Poisonous” disinformation and make a recurring 100% tax deductible donation (http://drrimatruthreports.com/index.php?page_id=189) to the Natural Solutions Foundation so that we can continue to provide information and strategic input to keep your health freedom free.

Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD

Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
www.NaturalSolutionsFoundation.org
www.Organics4U.org
www.NaturalSolutionsMarketPlace.org
www.NaturalSolutionsMedia.tv

1:12 PM

FOR IMMEDIATE RELEASE
Orthomolecular Medicine News Service, October 9, 2008

(OMNS, October 9, 2008) “Dietary supplements cause 600 ‘adverse events'”, reported USA Today on 22 Sept, 2008. In an article that looks much like an official US Food and Drug Administration press release, it said that “Serious side effects from the use of food supplements resulted in 604 “adverse-event” reports – a list that includes at least five deaths – through the first six months that such accounts have been required by law.” (1)

Good grief! Looks like all those supplement-popping health nuts really are nuts after all. Food supplements simply must be dangerous!

Or are they?

Later on in the article, far from the headline, USA Today conceded that “An adverse event can be anything from a concern that a supplement isn’t working to a serious illness that follows consumption.” And, FDA spokesman Michael Herndon admitted that of the five deaths and 85 hospitalizations reported, “Some of these deaths were likely due to underlying medical conditions.”

FDA’s method of gaining data is suspect at best and biased at worst. Their “Dietary Supplement Adverse Event Reporting” webpage,
http://www.cfsan.fda.gov/~DMS/ds-rept.html, states: “FDA would like to know when a product causes a problem even if you are unsure the product caused the problem or even if you do not visit a doctor or clinic.” The measure of uncertainty involved in publicly soliciting adverse reports “even if you are unsure that the product caused the problem” is noteworthy.

But most significant of all is that FDA refused to disclose exactly which supplements allegedly were causing problems. Doesn’t the public have a right to know? In the absence of FDA disclosure to the contrary, it is likely that the five or fewer deaths attributed to “food supplements” were in fact due to medicinal substances marketed as dietary supplements. FDA acknowledges this in a round-about way at their website
(http://vm.cfsan.fda.gov/~dms/mwgblghb.html).

There you will find an “Important Message” which asks health professionals to “Report Serious Adverse Events Associated with Dietary Supplements Containing GBL, GHB, or BD . . . a group of products sold as dietary supplements for bodybuilding, weight loss and sleep inducement which have been determined to pose a significant public health hazard. These products are chemically related ! to gamma butyrolactone (GBL), gamma hydroxybutyric acid (GHB), and 1,4 butanediol (BD), and can cause dangerously low respiratory rates (intubation may be required), unconciousness/coma, vomiting, seizures, bradycardia and death. GBL, GHB and BD have been linked to at least 122 serious illnesses reported to FDA, including three deaths.”

But these substances are not foods. They are not vitamins, and they are not minerals, and they are not amino acids. They should not be considered with or as food supplements. Over half of all Americans safely take nutritional supplements every day. If each of those persons took only one tablet per day, that would be some 145,000,000 individual doses daily, for a total of over 53 billion doses annually. Many healthy people take more. And yet, according to national statistics compiled by the authoritative American Association of Poison Control Centers, there is not even one death per year from vitamins. (2) Look at the reports, which detail each individual vitamin, mineral, amino acid and herb, and see for yourself at
http://www.aapcc.org/dnn/NPDS/AnnualReports/tabid/125/Default.aspx

By comparison, FDA acknowledges that prescription drugs resulted in 482,154 adverse-event reports in the year 2007. That is nearly 400 times as many adverse events from prescription drugs per six-month period. And this much higher number does not include over-the-counter drugs, a striking omission. Many non-prescription drugs, such as Tylenol (acetaminophen), are a long way from safe. Liver toxicity from acetaminophen poisoning is by far the most common cause of acute liver failure in the United States. Acetaminophen accounted for 51% of all acute liver failure cases in 2003. (3) Indeed, the Associated Press previously reported that common drug dangers are so bad that “Harmful reactions to some of the most widely used medicines – from insulin to a common antibiotic – sent more than 700,000 Americans to emergency rooms each year.” (4)

Vitamin supplements compete with FDA-sponsored drugs. FDA has been trying to eliminate availability of vitamin supplements for over 45 years. As early as 1962, writes constitutional attorney Jonathan W. Emord, “FDA perceived a competitive threat emerging to drug regulation from the sale of dietary ingredients at above RDA doses.” In 1966, “FDA published a rule that any dietary supplement exceeding 150% of the RDA for a vitamin or mineral would automatically be regulated as a drug.” In 1976, after a “public outcry,” the Proxmire Amendment prohibited FDA from deeming a vitamin or mineral a drug solely because of potency. “Undaunted,” continues Emord, “FDA tried yet again to rid the market of vitamins in the 1970s by claiming on a case by case basis that they were adulterated based on their potency.” FDA also tried to have supplements declared to be unapproved food additives. “FDA’s position was a logical absurdity: Single ingredient dietary supplements were food additives b! ecause the ingredients were added to a gelatin capsule which was, FDA said with a wink and a smirk, a food. . . The United States Court of Appeals for the Seventh Circuit described FDA’s position as an “Alice in Wonderland” approach.” In 1980, FDA tried to get vitamins classified as over-the-counter drugs. . . FDA has repeatedly exceeded the limits of its statutory authority to bring about changes designed to protect drug companies from competition.” (5)

Additional evidence comes directly from FDA, whose own Dietary Task Force Report, released June 15, 1993, said: “The task force considered many issues in its deliberations including to ensure that the existence of dietary supplements on the market does not act as a disincentive for drug development.” There is also this statement was made by FDA Deputy Commissioner for Policy David Adams, at the Drug Information Association Annual Meeting, July 12, 1993: “Pay careful attention to what is happening with dietary supplements in the legislative arena . . . If these efforts are successful, there could be created a class of products to compete with approved drugs. The establishment of a separate regulatory category for supplements could undercut exclusivity rights enjoyed by the holders of approved drug applications.”

FDA wants control of vitamins. Their latest ploy is to frighten the public into thinking vitamin supplements are dangerous, without proof, and without even naming the supplements they accuse. Don’t fall for what Abram Hoffer, M.D., calls “the FDA’s grand lie that, if told over and over again, is accepted as somehow true.”

Vitamin supplements are not the problem. Poor eating habits, and too many medicines, are the problem. Food supplements are a solution. They are effective, and vastly safer than drugs. The US Food and Drug Administration knows this full well.

References:

(1) Perez AJ. Dietary supplements cause 600 ‘adverse events’. USA Today, Sept 22, 2008:
http://www.usatoday.com/news/health/2008-09-22-supplements-adverse-events_N.htm
or http://www.usatoday.com/news/health/2008-09-22-supplements-adverse-events_N.htm?POE=click-refer

(2) Annual Reports of the American Association of Poison Control Centers’ National Poisoning and Exposure Database, 3201 New Mexico Avenue, Ste. 330, Washington, DC 20016. Download any report from 1983-2006 at
http://www.aapcc.org/dnn/NPDS/AnnualReports/tabid/125/Default.aspx
free of charge. The “Vitamin” category is usually near the end of the report. Summary and commentary at:
http://www.doctoryourself.com/vitsafety.html

(3) Larson AM et al Acetaminophen-induced acute liver failure: results from a United States multicenter, prospective study. Hepatology 2005;42:1364-1372. See also:
http://www.medpagetoday.com/Psychiatry/Depression/tb/2233

(4) Associated Press, Oct 17, 2006.
http://www.msnbc.msn.com/id/15305033/

(5) Emord JW. FDA violation of the rule of law. Speech from the Health Freedom Exposition in Richmond, Virginia September 23, 2006.
http://www.emord.com/events/speeches/fda_violation.htm

Nutritional Medicine is Orthomolecular Medicine

Orthomolecular medicine uses safe, effective nutritional therapy to fight illness. For more information:
http://www.orthomolecular.org

The peer-reviewed Orthomolecular Medicine News Service is a non-profit and non-commercial informational resource.

Editorial Review Board:

Damien Downing, M.D.
Harold D. Foster, Ph.D.
Steve Hickey, Ph.D.
Abram Hoffer, M.D., Ph.D.
James A. Jackson, PhD
Bo H. Jonsson, MD, Ph.D
Thomas Levy, M.D., J.D.
Erik Paterson, M.D.
Gert E. Shuitemaker, Ph.D.

Andrew W. Saul, Ph.D., Editor and contact person.
Email: omns@orthomolecular.org
http://alobar.livejournal.com/3062139.html

Categories : Activism, Blog / Vlog, Dietary Supplements, Disinformation, Get Involved, Medical Hazards, Miscellaneous, Privacy
Tags : Adverse Events, Dietary Supplements, Disinfomation, DSHEA, FDA, health freedom, Natural Solutions Foundation, NSF, Orthomolecular Medicine, Personal Freedom
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