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Archive for Organics – Page 14

GMO Files: Secret EU High Level Meeting to Force GMOs on Unwilling Public

By Administrator on November 2, 2008 No Comments

The Independent on Sunday, one of Britain’s leading newspapers, published the following report about a secret meeting in which each of the Prime Ministers of the EU’s 27 countries were asked to nominate a representative to attend a secret meeting designed to develop strategies to force GMOs on a vigorously resistant public.

In the EU, all GMO foods and ingredients must be clearly labeled although animals fed GMO feeds are not labeled despite the fact that their meat and other products contain GMO materials.

Predictably, there is a growing push back movement in the EU against this food tyranny. There needs to be more or same here since, according to a New York Times article, 87% of the American people want clear identification of any GMO products or ingredients in the “foods” they are eating.

More than 80% of all foods consumed in the US contain unlabeled and unidentified GMOs.

Please click here (http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=25920) to let your Congressional legislators know that you support the GMO safety and labeling legislation presented by Denis Kucinich (D-OH) and that you want them to support it and become co-sponsors of these bills.

And please forward this to your entire list so that they, too, can get their legislators on board. Now.

Thanks for your activism

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

Europe’s secret plan to boost GM crop production

Gordon Brown and other EU leaders in campaign to promote modified foods

By Geoffrey Lean
Sunday, 26 October 2008
GM corn growing in France, which has since suspended cultivation of modified crops

Gordon Brown and other European leaders are secretly preparing an unprecedented campaign to spread GM crops and foods in Britain and throughout the continent, confidential documents obtained by The Independent on Sunday reveal.

The documents – minutes of a series of private meetings of representatives of 27 governments – disclose plans to “speed up” the introduction of the modified crops and foods and to “deal with” public resistance to them.

And they show that the leaders want “agricultural representatives” and “industry” – presumably including giant biotech firms such as Monsanto – to be more vocal to counteract the “vested interests” of environmentalists.

News of the secret plans is bound to create a storm of protest at a time when popular concern about GM technology is increasing, even in countries that have so far accepted it.

Public opposition has prevented any modified crops from being grown in Britain. France, one of only three countries in Europe to have grown them in any amounts, has suspended their cultivation, and resistance to them is rising rapidly in the other two, Spain and Portugal.

The embattled biotech industry has been conducting a public relations campaign based round the highly contested assertion that genetic modification is needed to feed the world. It has had some success in the Government, where ministers have been increasingly speaking out in favour of the technology, and in the European Commission, with which its lobbyists have boasted of having “excellent working relations”.

The secret meetings were convened by Jose Manuel Barroso, the pro-GM President of the Commission, and chaired by his head of cabinet, Joao Vale de Almeida. The prime ministers of each of the EU’s 27 member states were asked to nominate a special representative.

Neither the membership of the group, nor its objectives, nor the outcomes of its meetings have been made public. But The IoS has obtained confidential documents, including an attendance list and the conclusions of the two meetings held so far – on 17 July and just two weeks ago on 10 October – written by the chairman.

The list shows that President Nicolas Sarkozy of France and Chancellor Angela Merkel of Germany sent close aides. Britain was represented by Sonia Phippard, director for food and farming at the Department of Environment, Food and Rural Affairs.

The conclusions reveal the discussions were mainly preoccupied with how to speed up the introduction of GM crops and food and how to persuade the public to accept them.

The modified products have to be approved by the EU before they can be sown or sold anywhere in Europe. But though the Commission officials are generally strongly in favour, European governments are split, causing the Council of Ministers, on which they are represented, to be deadlocked.

In that event the bureaucrats on the Commission wave them through anyway. They are legally allowed to do this, but overruled governments and environmental groups are unhappy.

The conclusions of the first meeting called for the “speeding up of the authorisation process based on robust assessments so as to reassure the public”, while the second one added: “Decisions could be made faster without compromising safety.”

But the documents also make clear that Mr Barroso is going beyond mere exhortation by trying to get prime ministers to overrule their own agriculture and environment ministers in favour of GM. They report that the chairman “recalled the importance for prime ministers to look at the wider picture”, “invited the participants to report the discussions of the group to their heads of governments”, and “stressed the importance of drawing their attention to ongoing discussions in the Council [of Ministers]”.

Helen Holder of Friends of the Earth Europe said: “Barroso’s aim is to get GM into Europe as quickly as possible. So he is going straight to prime ministers and presidents to tell them to step on their ministers and get them into line.”

The conclusions of the meetings on public opposition are even more incendiary. The documents ponder “how best to deal with public opinion” and call for “an emotion-free, fact-based dialogue on the high standards of the EU GM policy”. And they record the chairman emphasising “the role of industry, economic partners and science to actively contribute to such a dialogue”. He adds that “the public feels ill-informed” and says “agricultural representatives should be more vocal”. And in a veiled swipe at environmental groups he says that the debate “should not be left to certain stakeholders who have a legitimate but vested interest in it”.

http://www.independent.co.uk/environment/green-living/europes-secret-plan-to-boost-gm-crop-production-973834.html

Categories : Activism, Blog / Vlog, Buy-Cott, CODEX Consequences, Food Crisis, Get Involved, GMOs, International Cooperation, Miscellaneous, Organics, Privacy
Tags : GM, GMO, GMO Labeling, GMOs, health freedom, Natural Solutions Foundation, NSF, Secret EU Meeting

GM Files: US Election Results Won’t Help Solve GM Problem Without Public Pressure

By Administrator on November 2, 2008 No Comments

Neither Candidate for the office of President of the US is committed to controlling, labeling and eliminating GMOs.

That’s bad news for the environment and bad news for us.
But the situation is not hopeless. Take South Africa, for example.

Despite years of force feeding GMO staple foods, including white corn, which most of South Africa’s poor population lives on, the South African Government, despite a great deal of backing and filling, has finally made mandatory labeling of all GMO food and ingredients mandatory.

Why can’t we do the same? Why can’t we rouse enough outrage and pressure to force the US to retreat from its 1992 position, instituted upon the signing of an Executive Order by then-President George Bush Sr., making GMOs administratively (and pseudo-scientifically) “substantially equivalent” to non modified foods.

Science, on the other hand, makes it clear that nothing could be further from the truth. If you check out the GMO Files in this blog, you will find abundant – and very scary – data that makes it clear that these “foods” are not food at all, but industrial toxins.

Right now there are three laws before the US House of Representatives, sponsored by Rep. Denis Kuchinch (D, OH) which would require safety testing, labeling and scientific evaluation of all GMO crops and products.

Click here (http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=25920) to support those bills and ask your Congressional members to become both supporters and co-sponsors of this vitally important legislation.

In the meantime, I hope you will join the Natural Solutions Foundation’s vigorous and active No-GMO-Forum (http://groups.yahoo.com/group/no-genetically-modified-foods/join) and become part of the community of action to stop being fed industrial toxins instead of food, all with the connivance of the next POTUS (President of the United States).

And don’t forget to give generously to support the Natural Solutions Foundation as we keep health freedom free! Click here (https://staging.drrimatruthreports.com/index.php?page_id=189) to make your recurring, tax exempt donation and here (https://staging.drrimatruthreports.com/?page_id=1130) to order the best coffee in the world, our Valley of the Moon(TM) shade grown, chemical free coffee – ground or whole bean ~ A Little Bit of (NON GMO) Heaven in a Cup(TM) ~ while you support health freedom.

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

US election impact on GM food
By Sarah Hills, 31-Oct-2008 [www.nutraingredients-usa.com]

Genetically modified food companies should be paying particular attention to the results of next week’s presidential election as they could face tough times ahead, according to a Soil Association report. Click here () to read more.

Consumers, food manufacturers and farmers are increasingly moving away from GM products, the new study called Land of the GM-Free? How the American public are starting to turn against GM food, claimed.

At the same time the UK environmental charity said 87 percent of Americans want labels on food telling them whether Genetically Modified (GM) products have been used or not.

The SA added: “These developments, combined with the possibility of Democrat Presidential Candidate Barack Obama’s pledge to support legislation to label GM food if he should get elected, suggest that GM companies are in for a difficult few years in the USA.”

Categories : Autism, Blog / Vlog, Buy-Cott, Elections and Candidates, Fundraiser, GMOs, Legislation to Support, Medical Hazards, Miscellaneous, Organics
Tags : Big Agribiz, chemical free, coffee, Dr. Rima, GMO, GMO Files, GMOs, Health, health freedom, Natural Solutions Foundation, NSF, POTUS, Presidential Election, Rima E. Laibow, Rima E. Laibow MD, shade grown, Valley of the Moon, Valley of the Moon(TM)

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 (https://staging.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 (https://staging.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 (https://staging.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

“Breakthrough Death”: Newest Medical Innovations Can Be Way Too New

By Administrator on October 12, 2008 No Comments

National Solutions Foundation and www.HealthFreedomUSA.org always bring you urgent information about your health freedom and practical steps you can take to make a difference.

“Breakthrough casualty” (aka “collateral damage”) is what happens when a poorly tested, new drug or device (or novel GMO product) is publicized in the mass commercial media in ways that are not truthful and are misleading. Here are Action Steps To Help Prevent Yourself and Your Loved Ones From Becoming A “Breakthrough Casualty”

Today, the biggest causes of “breakthrough casualties” are the very issues that Natural Solutions Foundation has championed: GMOs, degraded organic standards, forced vaccinations and drugging, toxins (like pesticide residua, irradiation free-radicals, and the like) in the food chain, regulatory failures…

Action Items

Tell Your Legislators Compulsory Drugging, Including Vaccination is NOT OK!
http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=21833

Join the Natural Solutions Foundation’s No Forced Vaccination Yahoo! Forum
http://groups.yahoo.com/group/no-forced-vaccination/join

Support the Child Medication Safety Act So Schools Cannot Hold Parents Hostage For Refusing To Medicate Their Kids

http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=18970

Sign the Historic Tiburon Declaration Protecting Against Forced Vaccination
https://staging.drrimatruthreports.com/index.php?p=460

Join the free Health Freedom eAlerts Distribution List
https://staging.drrimatruthreports.com/index.php?page_id=187

Make Your Tax Deductible Contribution to the Natural Solutions Foundation to further our work.
https://staging.drrimatruthreports.com/index.php?page_id=189

Breakthrough Casualties…

You’ve heard of “Breakthrough Bleeding,” right? That’s when someone starts to bleed in spite of the fact that the body, or a drug, should be keeping them from doing that. Well, there’s another “Breakthrough” problem, and we are all vulnerable to it: “Breakthrough Death” which occurs when the latest medical “breakthrough” is so dangerous, so poorly tested, so poorly understood and so rapidly embraced by the ever-compliant media (“Ask your doctor is it’s right for YOU”) along with the ever time-pressured and sheepish medical practitioner that you, or someone you love, winds up dead or damaged because of a poorly understood, but hastily taken-up “Medical Breakthrough”.

The article posted below questions the wisdom of new medical “wisdom”. Indeed, the bone-fields of Medicine are littered with discarded ” breakthroughs”, too hastily approved, too gleefully adopted, too poorly tested. Of course, the graveyards of medicine are littered with the patients who blindly rushed to line up for the newest alleged “advances” and trusted the “wisdom” of the usually-well-meaning, carefully preselected and obedient sheep in MD’s clothing who blithely make their livings by being there with the new whatever-it-is-this-time. For example, in my educated opinion, the new chemotherapy which turns out to damage your heart and not work any better than any of the other ineffective conventional cancer approaches and, like every form of conventional chemotherapy, is a leading cause of NEW cancer in long term survivors; or the new antibiotic that turns out to cause your body to stop making any blood cells, red or white, or causes you to go deaf, or damages the dental integrity of your unborn child; or the new vaccine that turns out to cause healthy young girls and women to die or develop life threatening conditions; or the vaccine overload that turns so many happy young families into tragic families coping with the vaccine injury called autism, asthma, ADD/ADHD and a host of other names.

You get the idea.

What you may not know yet is that “fast track” approval for drugs and especially vaccines means that even the woefully inadequate safety assurances used by the FDA are shunted aside. And whether a drug, device or vaccine has been fast-tracked or not, that FDA approved-whatever is not deemed safe until after Phase IV Clinical Trials are completed and evaluated. And you may also not know that the FDA review committees and advisory committees, panels and boards are filled with people who have stocks, bonds, shares, patents and other direct financial conflicts of interest in the very products they are regulating, or seeking to evaluate and forbid if dangerous. Good system? For them, maybe. Just look at the state of American health and the trillions of dollars made by the illness care industry using things that make you sick and kill you although they have been through Phase I, II and II Clinical Trials. And although these devices, drugs and vaccines are now in their much-vaunted “Phase IV Clinical Trials”

What is a Phase IV Clinical Trial? It is the voluntary reporting, over time, of adverse reactions in the public. In other words, when doctors notice that patients are dying, or having strokes or heart attacks, or getting rather more cancer than “normal” or having more life-threatening asthma attacks or other reactions and the doctors involved bother to report (and often incriminate themselves if they were the ones who gave the drug or used the device in the first place), and these results pile up and the scientists reviewing these data do not have too many conflicts of interest, and their superiors in the system do not have too many conflicts of interest (which are now officially permitted by the agencies of the US Government charged with protecting our safety), then perhaps something will happen to remove this item from sale. But usually not. I need only say the word “Vioxx” and you get the idea. Or “Gardasil” or “Avienda”.

Or core systemic corruption and inability to protect the public… you get the idea. *

We like to think that clinical trials and other strategies protective of the public when using drugs, pesticides, vaccines and other toxins are iron clad and powerful. Nothing could be further from the truth. The FDA, EPA and USDA, the principle “guardians” of public health, do not allocate their funding efficiently to do their jobs. Congressional report after Congressional report, investigative piece after investigative piece makes that very clear. But the structure of these agencies themselves makes it even more clear.

For the FDA, a large proportion of whose operating budget comes from “user fees” which Pharmaceutical companies pay to have their products approved. Those user fees mean that the FDA is the client, not the regulator, of the drug industry.

Now it looks like the food industry will be asked to pay the same sort of user fees so the food side of the house will also become a client of the industry it allegedly regulates. Wonder what will happen to small local, organic producers in that regulatory world, where only the big and powerful are “too big to fail…”

Between the revolving door policy of the FDA, USDA, EPA and other federal agencies (through which high level employees are recruited from, revolve into, and continue to move back and forth between government, academia and industry as their careers develop) and the lack of oversight allowed or engaged in by these agencies, allowing “new breakthroughs” to create “new wealth” and “new disasters”.

Read the article below by a concerned and thoughtful Mom and take the Action Steps at the head of this article to make sure your State and National Legislators know that you do not want to be exposed to compulsory vaccination, a form of compulsory drugging.

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

–x–x–
Sometimes ‘new breakthroughs’ in medicine are too new

October 12, 2008
By Kimberly A. Brehm

Every time the medical community changes its mind and announces yet another way to care for your child, I’m amazed that my children made it out of their early years unscathed.

When my babies were young, they slept on their tummies, until the American Medical Association said the position could lead to sudden infant death syndrome. I bathed them in cool water when their fevers ran high, until I heard the tried-and-true practice could cause a seizure. And I gave them over-the-counter cold medicine when they had persistent, hacking coughs and sore throats.

Turns out that wasn’t a good idea, either.

On Tuesday, in response to concerns from medical experts that questioned whether cold and cough remedies do more harm than good to children, drug companies agreed to no longer make such medications for kids younger than 4.

Leading brands like Pediacare, Dimetapp, Robitussin, Triaminic and Little Colds no longer will continue to include dosage information for anyone younger than 4, and some pediatricians are asking the government to go further and ban such medicines for children younger than 6.

Each year, more than 7,000 children – mostly 2- and 3-year-olds – make a trip to the emergency room because of problems with over-the-counter cough and cold medicines. They usually have symptoms such as hives, drowsiness and unsteady walking. The Federal Drug Administration in 2007 pulled over-the-counter cough and cold medications for children younger than 6 to weigh their risks and effectiveness, but it could take another year or more before a final decision is reached.

Since it seems like every decade or so the medical community reverses previous decisions on particular medicines and medical treatments, it’s made me wonder when I can trust “new breakthroughs” and “innovative advances.”

A reversal about something like a cough suppressant – once seen as a benign drug – is the exact reason I have not yet allowed my teen daughters to be vaccinated with the HPV vaccine. It’s too new and hasn’t been researched enough for me to give my approval and feel comfortable.

In 2005, the Food and Drug Administration OK’d Gardasil as a vaccine against four strains of the human papillomavirus, or HPV, which can cause cervical cancer. Since then, more than 8 million girls ages 11 to 14 have been given the vaccine, and some states are considering making the shot mandatory for school enrollment, similar to other immunizations.

When Gardasil was approved a few years ago, my oldest daughter was 11, the ideal age to begin the shots. But I hesitated, thinking about other “new and improved” medicines that later proved to cause harm.

Remember when pregnant women were prescribed Thalidomide for nausea, then it was discovered to cause miscarriages and birth defects? Or when vaccines routinely included mercury, until that too proved to be dangerous? Or how about Fen-phen and Ephedra, which were supposed to be safe weight-loss drugs, and women began dying? In the 1990s, infants were given the rotavirus vaccine, until too many babies died after receiving it, and it was pulled from the market. I could go on and on listing dozens of examples like this, including strong, antidotal evidence of a link between immunizations and autism.

Thousands of parents of autistic children, including my brother and his wife, are firmly convinced their child’s autism was caused by vaccines and no amount of denial from drug companies would convince them otherwise.

And now, three years after young girls starting getting the Gardasil vaccine, it’s being investigated. There have been more than 9,000 complaints of serious ill effects filed with the Centers for Disease Control and Prevention, including blood clots, genital warts, paralysis and death.

The CDC said the deaths are not linked to Gardasil, but who knows what they’ll discover after further investigation? I personally am not willing to let my daughters be guinea pigs for the fairly new vaccine when even the CDC agrees the vaccine responds differently to each individual’s immune system and should not be mandatory for school participation.

“The overall effect of the vaccines on cervical cancer remains unknown. The real impact of HPV vaccination on cervical cancer will not be observed for decades,” the New England Journal reported in August. “With so many essential questions still unanswered, there is good reason to be cautious.”

When the wrong decision could cause your child harm – or maybe even result in death – it would be negligent not to be cautious. And when the medical experts change their minds every few years on what’s good and what’s harmful, it’s hard to make the right decision.
http://www.southtownstar.com/news/brehm/1213902,101208brehm.article
–x–x–

Please remember the six Action Steps you can take at the beginning of this posting.

(c) 2008

-x——————-x-
Footnote:

* Less than a year ago, a government study of the FDA concluded:

1) The FDA cannot fulfill its mission because its scientific base has eroded and its scientific organizational structure is weak.
2) The FDA cannot fulfill its mission because its scientific workforce does not have sufficient capacity and capability.
3) The FDA cannot fulfill its mission because its information technology (IT) infrastructure is inadequate.
4) FDA does not have the capacity to ensure the safety of food for the nation.
5) The development of medical products based on “new science” cannot be adequately regulated by the FDA.
6) There is insufficient capacity in modeling risk assessment and analysis.
7) The FDA science agenda lacks a coherent structure and vision, as well as effective coordination and prioritization.
8) The FDA has substantial recruitment and retention challenges.
9) The FDA has an inadequate and ineffective program for scientist performance.
10) The FDA has not taken sufficient advantage of external and internal collaborations.
11) The FDA lacks the information science capability and information infrastructure to fulfill is regulatory mandate.
12) The FDA cannot provide the information infrastructure support to regulate products based on new science.

[From: the November 2007 Report of the Subcommittee on Science and Technology, FDA Science and Mission at Risk]

Categories : Blog / Vlog, Buy-Cott, Cancer Assistance, CODEX Consequences, Elections and Candidates, Fundraiser, GMOs, Hall of Shame, Health Freedom Blog Home Page, Inspirational, Morgellon's Disease, Organics, Vaccination
Tags : Add new tag, Compulsory Drugging, Compulsory Vaccination, Dangerous Drugs, health freedom, Health Hazards, Mandatory Vaccination, medical hazards, Natural Solutions Foundation, NSF, Personal Choice, Vaccination
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