Landbouwgif als glyfosaat en atrazine zorgen voor alarmerende teruggang in vruchtbaarheid van de mens, dit nog naast de kankerverwekkende eigenschappen

In
een kort maar krachtig artikel stelt F. William Engdahl dat
het grootschalig gebruik van Monsanto’s glyfosaat en Syngenta’s
atrazine niet alleen de oorzaak zijn van kanker en andere ernstige
aandoeningen, maar schaden ook nog eens de menselijke voortplanting op een alarmerende manier……

In
1962 schreef zeebioloog Rachel Carlson een boek waarin ze
gedetailleerd inging op het gebruik destijds van het uiterst giftige DDT en het
effect van dit gif op levende wezens. Sindsdien hebben de grote
gifmengers hun les geleerd en weten hoe ze efficiënt de gevaren
van het gif dat ze produceren kunnen verdoezelen, o.a. middels een machtige lobby bij een groot aantal regeringen zoals die van de EU en haar lidstaten……

Pogingen
om glyfosaat te verbieden in de EU zijn al een paar keer gestrand
door de machtige lobby van de grote gifmengers, zelfs GroenLinks EU
grofgraaier Bas Eickhout stemde voor het langer toestaan van dit
kankerverwekkende en vruchtbaarheidsschadende gif…..
 

Volgens
Engdahl heeft dit alles te maken met eugenetica, al zo aangehangen
door nazi-Duitsland en volgens hem is het zelfs opzet om mensen minder
vruchtbaar te maken als wapen tegen de overbevolking, waarbij hij
bekende personen, als prins Philip (Groot-Brittannië) aanhaalt, die
daar uitlatingen over hebben gedaan. Zo zei deze prins (ha! ha! ha!)
ooit dat de menselijke kudde moet worden uitgedund en in een
voorwoord van het boek met de titel: ‘If I were an Animal’ (1986) zei
deze flapdrol dat hij het verleidelijk vond om in reïncarnatie te
geloven en dat hij dan hoopt terug te komen als een dodelijk
virus……….

Henry
Kissinger, de vreselijke oorlogsmisdadiger die als Obama volkomen
onterecht de Nobelprijs voor de Vrede kreeg heeft tijdens de Nixon en
Ford administraties in de VS geopperd dat het verminderen van de
wereldbevolking een absolute prioriteit moet zijn daar de groeiende
VS bevolking anders met grote tekorten aan grondstoffen e.d. zou
komen te zitten…….

Nog
zo één: opperploert Bill Gates die opmerkte dat de wereldbevolking
(op dat moment 6,8 miljard mensen groot, dit aantal was in april
2019 al gegroeid tot 7,7 miljard mensen) snel zou
groeien naar 9 miljard, volgens hem kunnen ‘we’ als ‘we’ goed ons best
doen met vaccins,
volksgezondheid en reproductieve gezondheidszorg dat aantal verminderen met 10 tot 15%…….. 

Lees
het schrijven van Engdahl en trek je eigen conclusie, zelf vind ik
het ver gezocht dat men doelbewust uit is op actief de
wereldbevolking te verminderen middels gif, immers daardoor zou ook
de elite getroffen kunnen worden, daar gif tegenwoordig overal
om ons heen is en zou zelfs op veel plekken in drinkwater zijn te vinden,
zoals hij zelf ook schrijft, maar toch je weet maar
nooit, de machtigen van de wereld zijn tot alles instaat………. (neem
als voorbeeld nogmaals de uitlatingen van prince Philip, Bill Gates en
Henry Kissinger, echter je kan ook bedrijven als Unilever nemen, met een
enorme ‘duurzaamheidscampagne’ verbergt dit bedrijf haar
verantwoordelijkheid voor het volpompen van mensen met het uiterst
slechte palmolie, dat niet alleen niet duurzaam is, maar ook nog eens
schadelijk is voor de gezondheid en zelfs winkelketen Ekoplaza doet hier aan mee, daar
veel van haar producten palmolie bevatten…… (er is maar één duurzame
vorm van palmolie >> die niet geoogst wordt!!)
 

An
Alarming Link Between Pesticides and Eugenics

F.
William Engdahl info@williamengdahl.com via aweber.com
 

 

Hello
Dear Readers,

I
want to share with you something I wrote regarding an alarming
research and new book documenting how common agriculture pesticide
chemicals, such as the most widely used Roundup with glyphosate and
Syngenta’s Atrazine, are having a devastating impact on human
fertility. Since the 1962 publication of the book Silent Spring by
the courageous American marine biologist, Rachel Carson, detailing
the toxic impact of the then-most widely used pesticide, DDT on
living creatures, the agrichemical industry has become far more
efficient at hiding the dangers in their toxins. Widespread efforts
to ban Roundup and glyphosate in the EU were sabotaged by a massive
campaign from the pesticide industry led by Monsanto-Bayer. It is
easy to think of eugenics, the race purity practiced by the Third
Reich as something in the past. Hardly. The same Bill Gates who is
pushing radical gene-edited vaccines for covid19 has backed eugenics
initiatives including vaccines to reduce population. The most
shocking about the piece contained here is that so little notice is
taken in mainstream media of the charges.

If
you have not yet please consider a
donation
of support for my voice. The relentless censorship of the Internet
and social media by the private corporate companies since the 2020
Coronavirus is alarming and can only be compared with book burnings
in the 1930s.

I
thank you for your interest and support,

William
Engdahl
www.williamengdahl.com

Will
Mankind Be Extinct In a Few Years?

By
F. William Engdahl
  

10 march 2021       

Will Mankind Be Extinct In a Few Years?  

                                                                                         
              

It’s
no secret that Bill Gates and the advocates of the UN Sustainable
Development Agenda 2030 are also devout promoters of human eugenics,
the “thinning of the Human Herd” as Britain’s misanthropic
Prince Philip once put it. Some such as Joachim Schnellnhuber,
climate adviser to the Pope, openly welcome a human population to
below one billion as “sustainable.” Now serious research is
emerging that one of the most effective reducers of the human
population is being spread by so-called “modern scientific
agriculture” through the select use of toxic agrochemicals,
pesticides deemed safe which are anything but safe.

According
to a new book by Dr Shanna Shaw,
Count
Down
,
the male sperm count in Western industrial countries, including the
EU and USA, is falling at a dramatic rate. Shaw estimates that over
the past four decades the average sperm count has dropped by 50% or
more. In other words a young male today seeking to have a family has
only half the sperm count his grandfather did. Shaw estimates that
unless toxic chemical exposures in agriculture and the environment
are dramatically altered, we may not have the ability to reproduce
naturally much longer and by 2050 most human beings in the industrial
countries, including China, will need technological assistance to
procreate.
[i]

Shaw’s
book is a further elaboration of a 2017 peer-reviewed scientific
paper which Shaw and colleagues published. In the paper, Shaw
carefully analyzed a total of 244 estimates of Sperm Concentration
and Total Sperm Count (TSC) from 185 studies of 42 935 men who
provided semen samples in 1973–2011. What they found was alarming
to the extreme, but beyond a few media headlines, no changes of
consequence resulted as the powerful agrochemical corporations such
as Bayer-Monsanto, Syngenta, DowDuPont (now Corteva) lobbied
regulators to ignore the findings.

Shaw
found that “Among Unselected Western studies, the mean Sperm
Concentration declined, on average, 1.4% per year with an overall
decline of 52.4% between 1973 and 2011.” The same group of males,
had “an average decline in mean TSC of 1.6% per year and overall
decline of 59.3%.” That is a sperm count decline as of a decade ago
of more than 59% in men, unselected by fertility, from North America,
Europe, Australia and New Zealand. And it continues to decline year
by year.
[ii]

Because
of lack of serious support for new studies, updated data is limited.
Fifteen years ago, over half of potential sperm donors in Hunan
Province, China, met quality standards. Now, only 18% do, a decline
blamed on endocrine disrupting chemicals according to one study. A
similar fall in sperm count was registered by researchers in Taiwan,
as well as a similar result for Israel. Shaw concludes, “male
reproductive health, not just semen quality by the way, is in
trouble, and this has consequences, not just for the ability to have
a child, but it also impacts the health of the man.” She cites as
examples, “low sperm count, infertility, testicular cancer, and
various general defects. One of them is undescended testicles,
another one is a condition where the opening of the urethra is not
where it should be…”
[iii]

Endocrine
Disruptors

Swan,
today with the Icahn School of Medicine at Mount Sinai in New York,
believes the cause is to be found in the huge rise in toxic chemical
exposures in recent decades, especially of chemicals known as
“endocrine disruptors” or hormone disruptors.  She points to
“chemicals that make plastics soft, which are phthalates, or
chemicals that make plastics hard like Bisphenol A, or chemicals that
are flame retardants, chemicals that are in Teflon, and so on,
pesticides…”
[iv]

The
last, pesticides, is the group that should send loud alarm bells
ringing because it is proven to get into groundwater and the human
food chain. Today the two most widely used pesticides in the world
are Bayer-Monsanto’s Roundup containing the probable carcinogen,
glyphosate, and Azatrine made by Syngenta, which today is owned by
ChemChina.

In
2010 a renowned University of California, Berkeley scientist, Tyrone
B. Hayes, professor of integrative biology, led a major study of the
effect of Atrazine exposure for frogs. He found that the pesticide,
widely used on US corn crops and sugarcane, wreaks havoc with the sex
lives of adult male frogs, emasculating three-quarters of them and
turning one in 10 into females. He found ,“These male frogs are
missing testosterone and all the things that testosterone controls,
including sperm.” Moreover Hayes noted that the 10% of frogs
exposed to Atrazine that “turn from males into females –
something not known to occur under natural conditions in amphibians –
can successfully mate with male frogs but, because these females are
genetically male, all their offspring are male.”
[v]
Hayes declared, “I believe that the preponderance of the evidence
shows atrazine to be a risk to wildlife and humans.”

Atrazine
is a potent endocrine disruptor. Atrazine is also the second-most
widely used herbicide in the US behind Monsanto’s glyphosate
product, Roundup. Despite the evidence, in a controversial ruling the
US Environmental Protection Agency, in 2007 ruled that “Atrazine
does not adversely affect amphibian sexual development and that no
additional testing was warranted.” End of story? Hardly. But in
2004 the EU banned Atrazine saying Syngenta failed to prove its
safety in drinking water.

Another
agrochemical that has been determined to be an endocrine disruptor is
Monsanto’s Roundup with glyphosate. Roundup is the world’s most
widely used pesticide, in over 140 countries including Russia and
China. Its use on US GMO crops has exploded in recent years as almost
90% of US corn is GMO, and a similar percent of its soybeans. Between
1996 when GMO Monsanto corn and soybeans were authorized in the USA,
and 2017, Americans’ exposure to the chemical grew 500 percent. It
has been tested in drinking water, cereals in stores and in urine of
pregnant women.
[vi]
Almost all meat and poultry is saturated with glyphosate from animal
feed.

A
recent study carried out in Australia by researchers at Flinders
University found that Roundup killed the cells that produce
progesterone in women, causing their levels to drop. Glyphosate and
Roundup have been “linked to birth defects, reproductive problems
and liver disease, and it has been shown to have the potential to
harm the DNA of human umbilical cord, placental and embryonic cells.”
[vii]

In
2015 scientists in Nigeria examined the effects of combined exposure
to both glyphosate and Atrazine on rats. They found the combination
was even worse with effects on sperm, testosterone synthesis and male
reproductive organs.

In
2016 China’s state-owned chemicals giant, ChemChina, bought
Syngenta for a colossal $43 billion. At the time ChemChina had
distribution rights in China and other Asian countries for Monsanto
Roundup as well. On the ChemChina website it lists Atrazine among the
herbicides it sells, calling it a “safe and efficient herbicide for
corn fields…” ChemChina is also the leading producer of
glyphosate for the Chinese agriculture market.
[viii]

Today
China is facing, by its own admission, a major agriculture crisis and
is also struggling with ways to insure food security. Reports are
that an increased role for GMO crops with Chinese patents will be a
central part of a new five year plan which would undoubtedly mean
using glyphosate and Atrazine. At the same time the state is
increasingly alarmed by the falling birth rate which has not improved
despite relaxations on the One Child policy. With Chinese farmers
using significant amounts of pesticide chemicals including glyphosate
and Atrazine to improve yields,  they are pursuing a disastrous
combination that will not only not solve the growing food crisis, but
also may destroy the reproductive potential of a major portion of its
890 million  rural population, as well as countless millions of
urban citizens. 

Are
these dangerous endocrine disrupting agrochemicals allowed worldwide 
because of bureaucratic ignorance of the damage caused by
glyphosates, Atrazine and other endocrine disrupters on the human
reproduction? Is it only because of corporate greed for hyper profits
that they exist? A 1975 quote from Henry Kissinger, author of the
eugenics document NSSM-200 during the Nixon-Ford era is instructive: 
“Depopulation should be the highest priority of foreign policy
towards the third world, because the US economy will require large
and increasing amounts of minerals from abroad, especially from less
developed countries.” And from Bill Gates: “The world today has
6.8 billion people…that’s headed up to about 9 billion. If we do
a really great job on vaccines, health care, reproductive health
services, we could lower that by perhaps 10 to 15 percent.” Or the
grand old dog of eugenics, Prince Philip: “I must confess that I am
tempted to ask for reincarnation as a particularly deadly virus.” ~
Prince Philip, in his Foreword to “If I Were an Animal” –
United Kingdom, Robin Clark Ltd., 1986.

We
are rapidly making the human species extinct as we continue to ignore
dangers of these toxins to human and other life forms.

Endnotes:

[i]
Sustainable Pulse, How Our Modern World Is Threatening Sperm Counts,
Altering Male and Female Reproductive Development, and Imperiling the
Future of the Human Race, February 26, 2021,
 
https://sustainablepulse.com/2021/02/26/count-down-how-our-modern-world-is-threatening-sperm-counts-altering-male-and-female-reproductive-development-and-imperiling-the-future-of-the-human-race/

[ii]
Shanna H. Swan et al,  Temporal trends in sperm count: a
systematic review and meta-regression analysis,

25 July 2017,  Human
Reproduction Update, Volume 23, Issue 6, November-December 2017,
Pages 646–659,
   
https://academic.oup.com/humupd/article/23/6/646/4035689

[iii]
Interview with Dr Swan, August 18, 2017,
https://www.loe.org/shows/segments.html?programID=17-P13-00033&segmentID=1

[iv]
Ibid.

[v]
Robert Sanders, Pesticide atrazine can turn male frogs into females,
March 1, 2010,  
https://news.berkeley.edu/2010/03/01/frogs/

[vi]
Isabelle Z., The dangers of glyphosate  the endocrine
disrupting synthetic herbicide, 14 April, 2019,  
https://www.cancer.news/2019-04-14-dangers-of-glyphosate-the-endocrine-disrupting-synthetic-herbicide.html

[vii]
Ibid.

[viii]
ChemChina website,
https://agr.chemchina.com/nonghuaen/cpyfw/qthgcp/webinfo/2011/12/1324534322971218.htm

Image: Unk Author: Unk License: CC0 public domain license Source: https://www.piqsels.com/en/public-domain-photo-jawoy

======================================

Zie ook: ‘Eugenetica en genetische manipulatie gaan hand in hand……‘ 

Pfizer Coronavirus vaccin: wat je niet wordt verteld over de vaccins tegen COVID-19‘ (ook een artikel van Engdahl)

Schouten (ChristenUnie minister) weigert te voldoen aan advies van de Gezondheidsraad zo min mogelijk landbouwgif te spuiten ter bescherming van omwonenden

Carola Schouten (minister ‘Christen’Unie) wil uiterst giftige bestrijdingsmiddelen nog langer toestaan

Ook zonder TTIP zwaar gif op je bord!! Ploumen (PvdA) heeft keihard gelogen over TTIP!! (en dat meer dan eens!)

Mijn excuus voor de vormgeving, krijg het niet op orde.

Pfizer Coronavirus vaccin: wat je niet wordt verteld over de vaccins tegen COVID-19

William
Engdahl heeft op New Eastern Outlook (NEO) een artikel geschreven over het Coronavaccin van Pfizer
en in feite over alle andere nu al bestaande vaccins (buiten de 3 in
het westen heeft bijvoorbeeld China er 5 die al worden ingezet).

Engdahl
zegt dat de techniek die gebruikt wordt experimenteel is en daar kan
niemand wat tegen in brengen. Pfizer stelt dat het spectaculaire
resultaten heeft behaald met de eerste tests op mensen. Daarvoor
wordt een experimentele techniek gebruikt bekend als genbewerking
(genenbewerking) en dan specifiek mRNA genbewerking, iets dat nooit
eerder werd gebruikt voor het maken van vaccins. Engdahl stelt dat
voor we ons blij maken voor enige bescherming tegen COVID-19
(middels een experimenteel vaccin, Ap), we eerst meer moeten weten over
deze radicale experimentele techniek en het gebrek aan precisie daarvan.

De
financiële wereld (stond en staat) op haar kop toen Pfizer en haar
Duitse partner BioNTech op 9 november aankondigden een vaccin tegen
het Coronavirus te hebben ontwikkeld dat voor 90% ‘effectief’ zou
zijn. Ook Toni Fauci, hoofd van het National
Institute of Allergy and Infectious Diseases (NIAID) is enthousiast,
terwijl de EU bekendmaakte 300 miljoen doses van dit kostbare vaccin
te hebben besteld bij Pfizer. Men denkt het virus de baas te zijn,
echter er zijn wel wat opmerkingen te maken over dit en andere
vaccins, juist door de gebruikte experimentele techniek…….

Albert
Bourla de CEO van Pfizer heeft zelf heel wat minder vertrouwen in het
vaccin, op de dag dat het nieuws over het vaccin bekend werd gemaakt
heeft hij 62% van zijn aandelen Pfizer van de hand gedaan……
(ofwel: als het vaccin werkelijk een wondermiddel is, zou hij nooit
z’n aandelen hebben verkocht, immers de aandelen Pfizer zullen juist
in waarde stijgen als alles volgens plan verloopt) Bourla heeft
e.e.a. al in augustus in werking gesteld, immers anders zou hij
beticht kunnen worden van het gebruikmaken van ‘inside information’
en dat zou in zijn geval strafbaar zijn……

Een
ander teken dat ‘we’ extra moeten oppassen voor we ons laten
vaccineren, is het feit dat alle westerse firma’s die werken aan een
vaccin, bij voorbaat laten vastleggen dat ze niet aansprakelijk zijn
voor eventuele ernstige bijwerkingen van het vaccin…… (wat mij
betreft een teken aan de wand….)

Bourla
heeft gelogen tegen de pers over het feit dat Pfizer geld had
gekregen van de Trump administratie voor onderzoek dat tot een vaccin
moest leiden, terwijl Pfizer in de zomer een contract met de overheid
sloot voor 100 miljoen dosis (van het toen nog in ontwikkeling zijnde
vaccin)….. BioNTech, de (kleine) Duitse partner van Pfizer, die de
mRNA techniek heeft ontwikkeld, heeft in september 2019 een overeenkomst
gesloten met de Bill & Melinda Gates Foundation. Deze overeenkomst
houdt in dat er in samenwerking aan ontwikkeling zal worden gewerkt
om de mRNA technologie te gebruiken in de strijd tegen kanker en HIV.
Een persbericht daarover: ‘The Gates Foundation sees BioNTech
potential
to ‘dramatically reduce global HIV and tuberculosis’, van 5
september 2019, ‘bestaat intussen niet meer……..’

BioNTech
werkt verder samen met Chinese bedrijven die dezelfde techniek hebben
gebruikt voor het maken van vaccins, die zoals gezegd al op grote
schaal worden ingezet……. Vaccins die met grote snelheid zijn
ontwikkeld en met even grote snelheid werden goedgekeurd voor gebruik
en dat in een alarmerende korte tijd…..

Zonder
zorgvuldige tests worden de vaccins ingezet, Engdahl wijst daarbij op
het ontbreken van dierproeven, echter die zijn in het geheel niet
nodig, althans als je zorgvuldig wilt werken en daar neemt men de
tijd niet voor, zelfs niet voor de vermaledijde dierproeven…….
Menselijke proeven gedaan in 3 maanden tijd zouden voldoende zijn,
echter daar is geen sprake van, 3 maanden is veel te kort voor een
nieuw vaccin waarvoor je eerder moet denken aan testen over een paar
jaar tijd…… Het is al alarmerend dat de grote farmaceuten zoals
gezegd elke verantwoording voor ernstige bijwerkingen in contracten
hebben afgewezen, echter volgens Engdahl is nog meer verontrustend
dat de mRNA techniek nooit eerder is toegestaan om te gebruiken voor
het testen van een vaccin……

Een
test met muizen waarbij deze genetisch gemanipuleerde mais te eten
kregen, besproeid met het glyfosaat rijke Roundup van Monsanto
resulteerde na negen maanden in kankers en (ernstige) beschadiging
van lever en andere organen…… Eerdere tests door Monsanto gaven
na 3 maanden geen enkel probleem en schunnig genoeg verwijst dat bedrijf uiteraard naar de korte testperiode….. (3 maanden, dezelfde tijd die
werd gebruikt voor de test van het Coronavaccin van Pfizer en
anderen)

Het op deze manier introduceren van een NB een experimenteel vaccin heeft alles te maken met de angstzaaierij van de Wereldgezondheidsorganisatie (WHO) over het Coronavirus………

Het
zal je duidelijk zijn dat niemand serieus kan stellen dat de vaccins
die snel op de markt komen veilig zijn, daarvoor is de ‘testtijd’
veel te kort….. Kortom je kan niet anders concluderen dan dat het
vaccin tegen COVID-19 potentieel gevaarlijk is en toch willen Fauci,
de EU en Pfizer liefst nog voor het eind van het jaar tientallen
miljoenen mensen vaccineren met dit (nogmaals) experimentele
vaccin……..  
 

Dr.
Romeo Quijano, oud-professor Farmacologie en Toxicologie aan de
universiteit van Manilla waarschuwt zelfs voor dit experimentele
vaccin, daar volgens hem e.e.a. kan leiden tot een versterking van
het Coronavirus, ja zelfs tot het ‘agressiever’ worden van het virus,
wat eerder in dierproeven werd geconstateerd….. Quijano waarschuwt
ervoor dat negatieve effecten maar al te vaak onder het tapijt worden
geveegd, immers er zijn belangen zoals die van farmaceuten in het
geding……. Hij haalt een ander door Gates gepromoot mRNA vaccin
van Moderna aan, waar 3 van de 15 menselijke experimenten met
een hoge dosis te maken kregen met ernstige medische symptomen…..
Moderna concludeerde echter dat het vaccin over het algemeen veilig
is en goed wordt verdragen…….   

Wat
betreft Moderna is het stuitend te zien dat de reguliere media
zonder enig onderzoek, laat staan kritiek, het vaccin de hemel in
hebben geprezen……  

Lees
het relaas van Engdahl en oordeel zelf of je wel of niet een vaccin
zal nemen…….. 
 

Nog even wat betreft
de kop van dat artikel: het precautionary principle ofwel het
voorzorgsprincipe
is een moreel en
politiek
principe dat stelt dat als een ingreep of een beleidsmaatregel
ernstige of onomkeerbare schade kan veroorzaken aan de samenleving of
het milieu, de bewijslast ligt bij de voorstanders van de ingreep of
de maatregel als er geen wetenschappelijke
consensus
bestaat over de toekomstige schade. Het
voorzorgsprincipe is vooral van toepassing in de gezondheidszorg en
het milieu; het gaat daar in beide gevallen over complexe systemen
waar ingrepen resulteren in onvoorspelbare effecten. (Wikipedia)

Why
We Need Precautionary Principle With Coronavirus Vaccines

F.
William Engdahl info@williamengdahl.com via aweber.com

What’s
Not Being Said About Pfizer Coronavirus Vaccine

By
F. William Engdahl 13 November, 2020 

 


Bill
Gates is actively financing and promoting new untested vaccines
supposed to keep us at least somewhat safe from a ghastly death from
the novel coronavirus and supposedly allow us to resume somewhat
“normal” lives. The Pharma giant Pfizer has now announced what
they claim were spectacular results in initial human tests. They use
an experimental technology known as gene editing, specifically mRNA
gene-editing, something never before used in vaccines. Before we rush
to get jabbed in hopes of some immunity, we should know more about
the radical experimental technology and its lack of precision.

The
financial world went ballistic on November 9 when the pharma giant
Pfizer and its German partner, BioNTech, announced in a company press
release that it had developed a vaccine for Covid19 that was “90%”
effective. The controversial US head of NIAID, Tony Fauci, rushed to
greet the news and the EU announced it had purchased 300 million
doses of the costly new vaccine. If you believe financial markets,
the pandemic is all but past history.

Suspicious
events

However
it seems Albert Bourla, the CEO of Pfizer, doesn’t share the
confidence of his own claims. On the day his company issued its press
release on the proposed vaccine trials, he sold 62% of his stock in
Pfizer, making millions profit in the deal. He made the sell order in
a special option in August so it would not appear as “insider
selling”, however he also timed it just after the US elections and
the mainstream media illegitimately declared Joe Biden
President-elect. It seems from appearances that Bourla had a pretty
clear conflict of interest in the timing of his press release on the
same day.
[i]

Bourla
lied and denied to press that his company had received any funds from
the Trump Administration to develop the vaccine when it came out they
contracted in summer to deliver 100 million doses to the US
Government. Further adding to the suspect actions of Pfizer was the
fact the company first informed the team of Joe biden rather than the
relevant US government agencies.

But
this is far from the only thing alarming about the much-hyped Pfizer
announcement.

The
German Partner

Pfizer,
famous for its Viagra and other drugs, has partnered with a small
Mainz, Germany company, BioNTech, which has developed the radical
mRNA technique used to produce the new corona vaccine. BioNTech was
only founded in 2008. BioNTech signed an agreement with the Bill &
Melinda Gates Foundation in September, 2019, just before announcement
in Wuhan China of the Novel Coronavirus and just before BioNTech made
its stock market debut. The agreement involved cooperation on
developing new mRNA techniques to treat cancer and HIV. Curiously
that press release, “The Gates Foundation sees BioNTech potential
to ‘dramatically reduce global HIV and tuberculosis’” 05.
September 2019, has now been deleted.

BioNTech
also has an agreement with one of the largest drug producers in
China, Shanghai Fosun Pharmaceutical Co., Ltd (“Fosun Pharma”) to
develop a version of its mRNA vaccine for novel coronavirus for the
Chinese market. Ai-Min Hui, President of Global R&D of Fosun
Pharma said in an August statement, “Dosing the first Chinese
subject with BNT162b1 marks a milestone of the global co-development
program in China. We are closely working with BioNTech and regulatory
authorities to evaluate the safety and efficacy of BNT162b1 and other
mRNA vaccine candidates…”
[ii]

This
means that the same German biotech company is behind the covid
vaccines being rushed out in China as well as the USA and EU. The
vaccine is being rushed through to eventual approval in an alarmingly
short time.

Both
US and EU authorities and presumably also Chinese, waived the
standard animal tests using ferrets or mice and have gone straight to
human “guinea pigs.” Human tests began in late July and early
August. Three months is unheard of for testing a new vaccine. Several
years is the norm. Because of the degree of global panic engendered
by WHO over the coronavirus, caution is thrown to the wind. Vaccine
makers all have legal indemnity, meaning they can’t be sued if
people die or are maimed from the new vaccine. But the most alarming
fact about the new Pfizer-BioNTech gene edited vaccine is that the
gene edited mRNA for human vaccine application has never before been
approved. Notably, two year peer reviewed tests with mice fed
genetically modified corn sprayed with Monsanto glyphosate-rich
Roundup first showed cancer tumors after nine months as well as liver
and other organ damage. Earlier Monsanto company tests ended at three
months and claimed no harm.
[iii]
A similar situation exists with the gene edited mRNA vaccines that
are being rushed out after less than 90 days human tests.

Explicitly
experimental”

Dr.
Michael Yeadon replied in a recent public social media comment to a
colleague in the UK, “All vaccines against the SARS-COV-2 virus are
by definition novel. No candidate vaccine has been… in development
for more than a few months.” Yeadon then went on to declare, “If
any such vaccine is approved for use under any circumstances that are
not EXPLICITLY experimental, I believe that recipients are being
misled to a criminal extent. This is because there are precisely zero
human volunteers for…whom there could possibly be more than a few
months past-dose safety information.”
[iv]

Yeadon
is well qualified to make the critique. As he notes in the comment,
“I have a degree in Biochemistry & Toxicology & a research
based PhD in pharmacology. I have spent 32 years working in
pharmaceutical R&D, mostly in new medicines for disorders of lung
& skin. I was a VP at Pfizer & CEO…. of a biotech I founded
(Ziarco – acquired by Novartis). I’m knowledgeable about new
medicine R&D.”
[v]
He was formerly with Pfizer at a very senior level.

Human
guinea pigs?

The
Pfizer-BioNTech vaccine is experimental and far from guaranteed safe,
despite the fact that Pfizer, the EU and the notorious Dr Tony Fauci
seem ready to roll it out even before year end to hundreds of
millions of humans.

The
experimental technology is based on a rather new gene manipulation
known as gene editing. In a major article in the 2018 New York
Council on Foreign Relations magazine,
Foreign
Affairs
,
Bill Gates effusively promoted the novel gene editing CRISPR
technology as being able to “transform global development.” He
noted that his Gates Foundation had been financing gene editing
developments for vaccines and other applications for a decade.
[vi]

But
is the technology for breaking and splicing of human genes so
absolutely safe that it is worth risking on a novel experimental
vaccine never before used on humans? Contrary to what Bill Gates
claims, the scientific answer is no, it is not proven so safe.

In
a peer reviewed article in the October, 2020 journal
Trends
in Genetics
,
the authors conclude that “the range of possible molecular events
resulting from genome editing has been underestimated and the
technology remains unpredictable on, and away from, the target
locus.”
[vii]

Dr.
Romeo Quijano, retired professor of Pharmacology and Toxicology at
the College of Medicine, University of the Philippines Manila, noted
some of the dangers of the experimental gene editing when applied to
human vaccines. Quijano warns of, “the danger that the vaccine
might actually “enhance” the pathogenicity of the virus, or make
it more aggressive possibly due to antibody-dependent enhancement
(ADE), as what happened with previous studies on test vaccines in
animals. If that should happen in a major human trial the outcome
could be disastrous. This serious adverse effect may not even be
detected by a clinical trial especially in highly biased clinical
trials laden with conflicts of interest involving vaccine companies.
Even when a serious adverse event is detected, this is usually swept
under the rug.” He cites the case of another Gates mRNA vaccine
candidate, Moderna, where “three of the 15 human experimental
subjects in the high dose group suffered serious and medically
significant symptoms. Moderna, however, concluded that the vaccine
was “generally safe and well tolerated,” which the
corporate-dominated media dutifully reported, covering-up the real
danger…”
[viii]

He
notes, “Exogenous mRNA is inherently immune-stimulatory, and this
feature of mRNA could be beneficial or detrimental. It may provide
adjuvant activity and it may inhibit antigen expression and
negatively affect the immune response. The paradoxical effects of
innate immune sensing on different formats of mRNA vaccines are
incompletely understood.” Quijano adds, “A mRNA-based vaccine
could also induce potent type I interferon responses, which have been
associated not only with inflammation but also potentially with
autoimmunity… and may promote blood coagulation and pathological
thrombus formation.”
[ix]

Quijano
writes in the extensively documented article, “among other dangers,
the virus-vectored vaccines could undergo recombination with
naturally occurring viruses and produce hybrid viruses that could
have undesirable properties affecting transmission or virulence.
The…possible outcomes of recombination are practically impossible
to quantify accurately given existing tools and knowledge. The risks,
however, are real, as exemplified by the emergence of mutant types of
viruses, enhanced pathogenicity and unexpected serious adverse events
(including death) following haphazard mass vaccination campaigns and
previous failed attempts to develop chimeric vaccines using genetic
engineering technology.”
[x]

Bill
Gates, the mRNA vaccine makers including Pfizer/BioNTech and Moderna,
and their close allies such as Dr. Tony Fauci of the NIAID are
clearly playing fast and loose with human lives in their rush to get
these experimental vaccines into our bodies. Notably, the same Dr.
Fauci and his NIAID owns the patent on a vaccine for dengue fever
known as  Dengvaxia, marketed by Sanofi-Pasteur and promoted as
an “essential” vaccine by Tedros’ WHO since 2016. Robert F.
Kennedy jr. noted that Fauci and NIAID “knew from the clinical
trials that there was a problem with paradoxical immune response,”
but they gave it to several hundred thousand Filipino kids anyway. It
was estimated that as many as 600 vaccinated children died before the
government stopped the vaccinations.
[xi]

Clearly
the well-established Precautionary Principle–if in serious doubt,
don’t– is being ignored by Fauci, Pfizer/BioNTech and others in
rushing to approve the new mRNA vaccine for coronavirus. Messenger
RNA technology has yet to produce an approved medicine, let alone a
vaccine.

 This
originally appeared on New Eastern Outlook online journal.

Endnotes:

 


[i]Shalini
Nagarajan, Pfizer’s CEO cashed out 60% of his stock on the same day
the company unveiled the results of its COVID-19 vaccine trial,
Novmber 11, 2020,
https://markets.businessinsider.com/news/stocks/pfizer-ceo-sold-stock-day-covid-19-vaccine-results-unveiled-2020-11-1029790705

[ii]BioNTech
and Fosun Pharma Announce Start of Clinical Trial of mRNA based
COVID 19 Vaccine Candidate in China, August 05, 2020, Source:
BioNTech SE,
https://www.globenewswire.com/news-release/2020/08/05/2073035/0/en/BioNTech-and-Fosun-Pharma-Announce-Start-of-Clinical-Trial-of-mRNA-based-COVID-19-Vaccine-Candidate-in-China.html

[iii]Seralini,
Gilles-Eric et al,  Long-term toxicity of a Roundup herbicide
and a Roundup-tolerant genetically modified maize, 24 June 2014,
Environmental Sciences Europe volume 26, Article number: 14 (2014),
https://enveurope.springeropen.com/articles/10.1186/s12302-014-0014-5

[iv]Dr
Michael Yeadon, open social media comment,
https://threadreaderapp.com/thread/1302725167588798467.html

[v]Ibid.

[vi]Bill
Gates, Gene Editing for Good: How CRISPR Could Transform Global
Development,

https://www.foreignaffairs.com/articles/2018-04-10/gene-editing-good?cid=nlc-fa_fatoday-20180601

[vii]Burgio,
G., & Teboul, L.,  Anticipating and identifying collateral
damage in genome editing, Trends in Genetics, 8 October 2020,
https://www.sciencedirect.com/science/article/pii/S016895252030247X

[viii]Romeo
F. Quijano, MD, Hazards of the COVID19 vaccine, August 21, 2020, 
https://www.bulatlat.com/2020/08/21/hazards-of-the-covid-19-vaccine/

[ix]Ibid.

[x]Ibid.

[xi]Joseph
Mercola,  The Well Known Hazards of Coronavirus Vaccines, May
11, 2020, 

https://www.lewrockwell.com/2020/05/joseph-mercola/the-well-known-hazards-of-coronavirus-vaccines/

=================================================

Zie ook: ‘Vaccin AstraZeneca in twee delen voor 90% beschermend tegen COVID-19 en de bijwerkingen…… (?)

De rijke landen behartigen tijdens de Coronacrisis de belangen van ‘Big Pharma’ i.p.v. de gezondheid van miljarden

Coronavirus: opmerking bij vaccins‘ (weggecensureerd, zie het bericht voor verdere info)

Ausweis bitte! COVI-PASS ‘noodzakelijk’ bij aantonen ‘immuniteit’ voor Coronavirus‘ (o.a. over het eerste bedrijf dat bezig is met het ontwikkelen van zo’n pas……)

Burgerrechten waaronder privacy aangetast door ‘strijd’ tegen het Coronavirus

Wereldbevolking moet afhankelijk worden gemaakt van vaccins in combinatie met een ‘vaccinatiepaspoort’‘ (zie ook de video’s in dat bericht, waarvan de hieronder getoonde er één is)

Forced vaccinations for all. And that means you. A triumph for authoritarians (een video uit 2018, zeker zien mensen!): 

Bill Gates’ inzet tegen het Coronavirus en zijn handelen op vaccinatiegebied: de winsten van de farmaceuten vermenigvuldigen

VS geeft 1 miljard dollar voor vaccin tegen COVID-19 aan Britse farmaceut‘ (een bericht van 25 mei 2020!!!!)

GSK
koopt belang in Duitse ontwikkelaar Coronavaccin CureVac, terwijl
minister de Jonge waarschijnlijk alweer een bok heeft geschoten
‘ (en zie de links in dat bericht) 

De WHO is bijkans overgenomen door de grote farmaceuten; juist van groot belang door de Coronacrisis

Artsen
en andere medici krijgen steeds meer weerstand voor kritiek op
vaccinatieprogramma’s: ‘leve de lobby’ voor de farmaceutische industrie

COVID-19:
wellicht zijn 2 vaccinaties nodig zegt farma lobbyist Osterhaus,
vandaag zijn dat er al 3: ping ping kassa!!

Een
vaccin tegen COVID-19 voor iedere VS burger zou onhaalbaar zijn en het
vaccineren van de hele wereldbevolking zou minstens 3 jaar tijd in
beslag nemen

Corona-angst: psychologische oorlogsvoering tegen de bevolking‘ 

Coronavirus: farmaceuten zijn nu al doende de prijs voor een vaccin op te drijven‘ (bericht van maart dit jaar)

Coronavirus: Roche laat zien waar farmaceuten voor staan: inhumaniteit, zelfzucht en bakken geld verdienen

Janssen (farmaceut) werkt aan een toekomst ‘waarin ziektes tot het verleden behoren…..’ ha! ha! ha! ha! ha!‘ 

Judy Mikovits, biochemicus in microbiologie, gevangengezet op aanwijzing van de farmaceuten‘ (!!!!) (een bericht uit 2019, dat over het griepvirus gaat en waarvan je de haren te berge zullen rijzen…..)

Farmaceuten moeten door het Internationaal Strafhof (ICC) worden berecht voor massamoord, chantage en machtsmisbruik 

En terzijde: ‘Rutte waarschuwt met z’n hamer indirect de bevolking ‘Coronavoorzichtig’ te zijn daar hij anders de feestdagen in het water laat donderen

Eugenetica en genetische manipulatie gaan hand in hand……

Eugenetica,
de leer van het telen van een meesterras had in de 20ste eeuw fikse aanhang onder
organisaties voor ‘het goede doel’, zoals de Rockefeller Foundation,
de Ford foundation (Henry Ford was een nazi aanhanger en daarmee een
nazi) en die van andere welgestelde families. 
Het ging zelfs zover dat de Rockefeller Foundation het eugenetica onderzoek van de nazi’s voor een groot deel financierde…… 

Na WOII heeft men de
term ‘eugenetica’ ingeruild voor ‘genetica’, daar de nazi’s zoals
bekend dik bezig waren met eugenitica en tja daar wilde men na WOII niet meer mee geconfronteerd worden……. Hoewel men de Duitse wetenschappers die zich met deze Frankenstein wetenschap bezig hielden na WOII naar de VS haalde….. (waar ze elke straf ontliepen voor hun gruwelijke werk, waar ze o.a. concentratiekampgevangenen voor gebruikten….)

Volgens
William Engdahl, die een boek schreef over de materie, is dat de
oorsprong van het manipuleren van genetische eigenschappen van planten. De Rockefeller
Foundation was de eerste die dit financierde en propageerde.  Engdahl stelt dat we er geen weet van hebben dat dergelijke
liefdadigheidsinstellingen, nu inclusief de ‘Bill and Melinda Gates
Foundation’, plus de Wereldgezondheidsorganisatie (WHO) en meerdere landen, met deze genetische manipulatie bezig zijn dan wel e.e.a. financieren…..

Volgens
Engdahl bestaat er een plan om via voedsel de wereldbevolking te
reduceren. Lijkt me ‘wat ver gezocht’, echter als je ziet waar
bijvoorbeeld een land als de VS mee bezig is, zou het me niet
verbazen, de wellust van de werkelijke machthebbers kent totaal geen
grenzen meer……

Lees
het schrijven van Engdahl en oordeel zelf. Het gaat hier wel om het
promoten van een boek dat Engdahl schreef ‘
Seeds
of Destruction: The Hidden Agenda of Genetic Manipulation’, onder het
schrijven van Engdahl vindt je een link naar een aantal pagina’s uit
dat boek. Nogmaals, lees het schrijven van Engdahl en oordeel zelf:

F.
William Engdahl
 info@williamengdahl.com via aweber.com

On
Creation of an Arctic Doomsday Seed Vault – Bill Gates, Rockefeller
and the GMO giants know something we don’t

Hello
again dear reader,

For
this edition of my complimentary newsletter I want to share with you
something I actually wrote back in 2007 almost a decade ago. Before I
do so, I want to say a few words about how I came to the theme of
Genetic Manipulation of Organisms (GMO), a subject which has
commanded a significant part of my research now for more than a
decade.  

In
2005 I was asked by the person who did the Croatian language
translation of my best-known work, 
A
Century of War: Anglo-American Oil Politics
,
if I would be willing to research a new book on the dangers of GMO.
Croatia, the devastating decade of war over, was in the process of
membership into the European Union and many there rightly feared that
EU trade rules would open the natural food production of Croatia to
industrially-produced non-nutritious food and to GMO crops. There was
a big debate in Croatia at the time over the health and safety of GMO
crops.

The
translator, Nedjeljka Batinović, had founded a new, independent
publishing house with her partner, and convinced me to undertake the
project. The world premiere of my best-selling book, 
Seeds
of Destruction: The Hidden Agenda of Genetic Manipulation
,
as a result, was in Zagreb in 2005, under the title, SJEME UNIŠTENJA.
What drove the book and my passion to uncover one of the most
incredible manipulations of the human food chain as well as the human
species, was my discovery that the origins of the entire manipulation
of traits of crop genes to alter their expression came from the
Rockefeller Foundation.

Armed
with only that one investigative lead, I embarked on one of the more
remarkable research efforts of my career. A hunch led me to look for
links between the Rockefeller family, their “philanthropic”
foundations, and eugenics, the fake 19th century religion of a master
race that argued humans should be bred like horses for desired traits
and undesired be killed off. To many my thesis seemed mad. Who after
all in their right mind would try to kill off normal people with
food? The book documented the shocking century-long obsession of the
family Rockefeller and other wealthy families with eugenics, renamed
by them as “genetics.” The book that resulted, which has
since been published in 15 foreign languages, to date to my
knowledge, is the only book that documents the firm link between GMO
and eugenics. The following piece documents another face of that
eugenics agenda, namely the attempt by the Rockefellers, Bill and
Melinda Gates Foundation, the Ford Foundation, the World Health
Organization and various governments to impose drastic world
population reduction in the name of the “Good.”

If
the safety and security of food for you and your family is important,
I urge you to buy my book, Seeds of Destruction and form your own
judgment about the risks of GMO.

For
a better reading experience I converted the text to a pfd-file which
You can find in the attachment of this mail. It’s 16 pages in A4
format.

Thank
you again for your interest,

F.
William Engdahl

www.williamengdahl.com

—————————————————————————————————————-

What
customers are saying about 
Seeds
of Destruction: The Hidden Agenda of Genetic Manipulation
:

“Most
Important Book of this New Century” 

David Chu

“Get
ready to have your eyes opened, big-time.” 

Laura

“Could
not put it down till I read it through.” 

Blue Rabbit

“Thank
you Mr. Engdahl for this well written book!” 

Lori “The Rogue Reader Mom”

“Everyone
Should Read This Book” 

DeannaF

“This
is an absolute must read…” 

Eternal Howl

“Five
Stars” 

lizzee.d

“A
must read for anyone new to the GMO controversy” 

Rebecca Alden

“An
informative, factual wild ride accounting that reads like a good spy
novel” 

MaryAnn

“I
highly recommend that everyone…give this book a read.” 

Anne Mendenhall

“WARNING:
If you are timid and faint of heart, do not read “SEEDS of
DESTRUCTION” by F. William Engdahl. Instead, go back to sleep,
and take comfort in being lied to by American corporations and U.S.
governmental agencies. After all, ignorance is bliss. Otherwise,
“SEEDS of DESTRUCTION” is a MUST-READ book” 

Justin Time

=================================

Hier de link naar pagina’s van Engdahls
boek, waarin hij o.a. spreekt over de genetisch gemanipuleerde zaden van Monsanto en andere grote bedrijven, die maar één doel voor ogen hebben: de wereldvoedselproductie controleren en bedienen, niet alleen middels het genetisch manipuleren van planten, maar ook via het genetisch manipuleren van dieren……

Zie ook: ‘Corruptie: Europese Commissie maakt gemene zaak met Monsanto over toestaan glyfosaat!‘ In dit bericht een aantal links over glyfosaat, Monsanto, enz.

Untitled Post

Corruptie:
Europese Commissie
maakt gemene zaak met Monsanto over toestaan
glyfosaat!

In
een uitgebreid schrijven toont William Engdahl aan (hij is economie onderzoeker,
historicus en journalist) dat Monsanto en de Europese Commissie
onder één hoedje hebben gespeeld, om glyfosaat, een onderdeel van
Monsanto’s Roundup, op de EU markt te houden……..

Voorts
toont Engdahl aan dat het onderzoek van Monsanto naar de effecten van
haar gif op de gezondheid, totaal onvoldoende was en dat een echt
wetenschappelijk onderzoek wel degelijk aantoont dat glyfosaat
kankerverwekkend is!!

Engdahl
spreekt zelfs onomwonden over corruptie: “
In
this installment I want to share with you something I have written on
one of the most shocking corruption scandals in the history of a very
corrupt European Union Commission together with corruption by
Monsanto and the related GMO agribusiness industry”.
 Een Nederlandse wetenschapper, Harry Kuiper speelt ook een smerige rol in het geheel, deze plork pleit er voor de regulering op GMO zaden (o.a. van Monsanto en haar opkoper Bayer) te verzwakken en het gebruik van deze zaden toe te staan in de EU

Lees
over de hele smerige gang van zaken aangaande het toestatan van een
kankerverwekkend gif, dat ook jij al jaren binnenkrijgt, althans als je niet jouw producten in een ecologische levensmiddelenzaak, dan wel op een
ecologische groentemarkt kocht/koopt…..

Ten
overvloede blijkt nogmaals dat de overheid allesbehalve oog heeft
voor uw gezondheid en veiligheid, maar wel voor de financiële belangen
van (grote) bedrijven en aandeelhouders…… De overheid in deze, de Europese
Commissie, is ook nog eens een niet democratisch gekozen orgaan, waarin godbetert de enorme PvdA kwal Timmermans zitting heeft…… Moet
je nagaan: men geeft als excuus voor het geven van extreem hoge inkomens en onkostenvergoedingen in het EU parlement,
zoals die aan politici en nog hogere inkomens voor figuren als Timmermans, dat men
dan niet ‘vattelijk’ is voor corruptie…. ha! ha! ha! ha! ha! ha! ha!

Nogmaals: NEXIT NU!

Cancerous
rats, corruption and Terminator seeds

©
F. William Engdahl

The
Cancer of Corruption in Brussels

September
2012 a respected international scientific journal, 
Food
and Chemical Toxicology
,
released a study by a team of scientists at France’s Caen
University led by Professor Gilles-Eric Seralini. The Seralini study
had been reviewed over a four-month period by a qualified group of
scientific peers for its methodology and was deemed publishable.

It
was no amateur undertaking but rather, the carefully-documented
results of tests on a group of 200 rats over a two-year life span,
with one group of non-GMO fed rats, a so-called control group, and
the other a group of GMO-fed rats.

Significantly,
following a long but finally successful legal battle to force
Monsanto to release the details of its own study of the safety of its
own NK603 maize, Seralini and colleagues reproduced a 2004 Monsanto
study published in the same journal and used by the European Food
Safety Authority (EFSA) for its 2009 positive evaluation of NK603.

Seralini’s
group based their experiment on the same protocol as the Monsanto
study but, critically, testing more parameters more frequently. And
the rats were studied for much longer—their full two year average
life-time instead of just 90 days in the Monsanto study. The long
time span proved critical. The first tumors only appeared 4 to7
months into the study. In industry’s earlier 90-day study on the same
GMO maize Monsanto NK603, signs of toxicity were seen but were
dismissed as “not biologically meaningful” by industry and EFSA
alike. It seems they were indeed very biologically meaningful.

The
study was also done with the highest number of rats ever measured in
a standard GMO diet study. They tested “also for the first time 3
doses (rather than two in the usual 90 day long protocols) of the
Roundup-tolerant NK603 GMO maize alone, the GMO maize treated with
Roundup, and Roundup alone at very low environmentally relevant doses
starting below the range of levels permitted by regulatory
authorities in drinking water and in GM feed.” 
[1]

Their
findings were more than alarming. The Seralini study concluded, “In
females, all treated groups died 2–3 times more than controls, and
more rapidly. This difference was visible in 3 male groups fed GMOs.
All results were hormone and sex dependent, and the pathological
profiles were comparable. Females developed large mammary tumors
almost always more often than and

before
controls; the pituitary was the second most disabled organ; the sex
hormonal balance was modified by GMO and Roundup treatments. In
treated males, liver congestions and necrosis were 2.5–5.5 times
higher. This pathology was confirmed by optic and transmission
electron microscopy. Marked and severe kidney nephropathies were also
generally 1.3–2.3 greater. Males presented 4 times more large
palpable tumors than controls…” 
[2]

Four
times meant four hundred percent more large tumors in GMO fed rats
than in normally fed ones of the control group. Moreover, they
reported, “By the beginning of the 24th month, 50–80% of female
animals had developed tumors in all treated groups, with up to 3
tumors per animal, whereas only 30% of controls [
non-GMO-fed—w.e.]
were affected. The Roundup treatment groups showed the greatest rates
of tumor incidence with 80% of animals affected with up to 3 tumors
for one female, in each group.” 
[3]

Such
alarming results had not yet become evident in the first 90 days, the
length of most all Monsanto and agrichemical industry tests to date,
a clear demonstration of how important it was to conduct longer-term
tests and apparently why the industry avoided the longer tests.

Seralini
and associates continued to document their alarming findings: “We
observed a strikingly marked induction of mammary tumors by R
(Roundup) alone, a major formulated pesticide, even at the very
lowest dose administered. R has been shown to disrupt aromatase which
synthesizes estrogens (Richard et al., 2005), but to also interfere
with estrogen and androgen receptors in cells (Gasnier et al., 2009).
In addition, R appears to be a sex endocrine disruptor in vivo, also
in males (Romano et al., 2010). Sex steroids are also modified in
treated rats. These hormone-dependent phenomena are confirmed by
enhanced pituitary dysfunction in treated females.” 
[4]

Roundup
herbicide, by terms of the license contract with Monsanto, must be
used on Monsanto and most other GMO seeds. The seeds are in fact
“modified” only to resist the weed-killing effect of Roundup, the
world’s largest-selling weed-killer.

In
plain language, as another scientific study noted, “GMO plants have
been modified to contain pesticides, either through herbicide
tolerance or by producing insecticides, or both, and could therefore
be considered as ‘pesticide plants’” 
[5]

Further,
“Roundup Ready crops [
such
as Monsanto NK603 maize-w.e.
]
have been modified in order to become insensitive to glyphosate. This
chemical, together with adjuvants in formulations, constitutes a
potent herbicide. It has been used for many years as a weed
killer…GMO plants exposed to glyphosate-based herbicides such as
Roundup…can even accumulate Roundup residues throughout their
life…Glyphosate and its main metabolite AMPA (with its own
toxicity) are found in GMOs on a regular and regulatory basis.
Therefore, such residues are absorbed by people eating most GMO
plants (as around 80% of these plants are Roundup tolerant).” 
[6]

Monsanto
had repeatedly refused scientific requests to publish the exact
chemicals used in its Roundup aside from one—glyphosate. They
argued that it was a “trade secret.” Independent analyses by
scientists indicated, however, that the combination of glyphosate
with Monsanto’s mystery added chemicals created a highly toxic
cocktail that was shown to toxically affect human embryo cells in
doses far lower than used in agriculture.
[7]​​​​​​​

Mammary
tumors that developed in rats fed GMO corn and/or low levels of
Roundup. From the paper “Long term toxicity of a Roundup
herbicide and a Roundup-tolerant genetically modified maize,”
published in 
Food
and Chemical Toxicology
.

​​​​​​​

What
was more than alarming in the context of that first long-term
independent study of the effects of a GMO diet on rats was that it
took place some twenty years after US President George H.W. Bush gave
the commercial release of GMO seeds the green light and mandated no
government safety tests before release. Bush did so following a
closed-door meeting with top officials of Monsanto Corporation, the
world’s largest GMO concern. The US President decreed that GMO
seeds were to be permitted in the United States with not one single
independent precautionary government test to determine if they were
safe for human or animal consumption. It became known as the Doctrine
of Substantial Equivalence, about which more in a subsequent chapter.
The EU Commission dutifully aped the US Substantial Equivalence
Doctrine of “hear no bad effects, see no bad effects…hear no
evil, see no evil.”

EFSA
‘science’ exposed

What
the Seralini study set off was the scientific equivalent of a
thermonuclear explosion. It exposed the fact that the EU “scientific”
controls on GMO were nothing other than accepting without question
the tests given them by Monsanto and the other GMO companies
themselves. As far as the irresponsible bureaucrats of the EU
Commission were concerned, when it came to GMO, the Monsanto fox
could indeed “guard the hen house.”

Suddenly,
with worldwide attention to the new Seralini results, the EU
Commission and its EFSA was under fire as never in their history. How
they reacted was worthy of a bad copy of an Agatha Christie murder
novel. Only it was no novel but a real-life conspiracy (yes,
Virginia, there are conspiracies in the real world…). The
conspiracy evidently involved some form of collusion between Monsanto
and the GMO agrichemical cartel, EU commissioners, the GMO panel
members of EFSA, complacent major media and several member
governments of the EU, including Spain and Holland.

The
Brussels EU scientific food regulatory organization, EFSA, was under
the gun from the damning results of the long-term Seralini study.
EFSA had recommended approval of Monsanto’s NK603 Roundup-tolerant
maize in 2009 without first conducting or insuring any independent
testing. They admitted in their official journal that they relied on
“information supplied by the applicant (Monsanto), the scientific
comments submitted by Member States and the report of the Spanish
Competent Authority and its Biosafety Commission.” EFSA also
admitted that the Monsanto tests on rats were for only 90 days.
Seralini’s group noted that the massive toxic effects and deaths of
GMO-fed rats took place well after 90 days, a reason why longer-term
studied were obviously warranted. 
[8]

The
Spanish report cited by EFSA was itself hardly convincing and was
anything but independent. It stated, “according to the current
state of scientific knowledge and after examining the existing
information and data provided by the Monsanto Company, the Spanish
Commission on Biosafety could give a favorable opinion to the
commercialization in the EU of maize NK603…” And the scientific
comments submitted by Member States seemed to include Spain and
Holland which applied to license the Monsanto seed in the first
place. 
[9]

The
EFSA concluded at the time of its approval in 2009 that, “the
molecular data provided [
by
Monsanto-w.e.
]
are sufficient and do not raise a safety concern.” The Brussels
scientific panel further declared amid scientific-sounding verbiage
that, “The EFSA GMO Panel is of the opinion that maize NK603 is as
safe as conventional maize. Maize NK603 and derived products are
unlikely to have any adverse effect on human and animal health in the
context of the intended uses.” 
[10]

Now,
in September 2012, three years after the commercial introduction of
Monsanto GMO maize in the EU, Seralini showed, complete with ghastly
photos, that Monsanto’s GMO maize demonstrably caused severe rates
of cancerous tumors and early death in rats.

The
EU Commission in Brussels had stated clear guidelines that were as
revealing for what they did not say as for what they did say about
what precautions are taken to insure public health and safety from
exposure to GMO plants and their paired toxic herbicides:
“Toxicological assessments on test animals are not explicitly
required for the approval of a new food in the EU or the US.
Independent experts have decided that in some cases, chemical
analyses of the food’s makeup are enough to indicate that the new
GMO is substantially equivalent to its traditional counterpart…In
recent years, biotech companies have tested their transgenic products
(maize, soy, tomato) before introducing them to the market on several
different animals over the course of up to 90 days. Negative effects
have not yet been observed.” 
[11]

Because
of US Government arm-twisting and of the obviously powerful lobby
power of the Monsanto-led GMO agrichemical lobby in the US and EU, as
of the time of the Seralini study, no regulatory authority in the
world had  requested mandatory chronic animal feeding studies to
be performed for edible GMOs and formulated pesticides. The only
studies available were a tiny handful of 90 day rat feeding trials
carried out by the biotech industry and no studies longer than that,
apparently on the principle that conflict of interest in an area as
important as the safety of food should not be taken as a serious
matter.

Revealingly,
the EU stated publicly the following seemingly reassuring policy:
“GMO critics claim that feeding studies with authorized GMOs have
revealed negative health effects. Such claims have not been based on
peer-reviewed, scientifically accepted evaluations. If reliable,
scientific studies were to indicate any type of health risk, the
respective GMO would not receive authorization.” 
[12] That
was the EU official line until the 2012 Seralini bomb exploded in
their faces.

EU
Commission coverup

The
September 2012 Seralini study was peer-reviewed, and it was published
in a highly respected international scientific journal after such
review. What was the response of the EU Commission and the EFSA?
Nothing short of fraudulent deception and coverup of their corruption
by the Monsanto GMO lobby.

On
November 28, 2012, only a few weeks after the study was published,
EFSA in Brussels issued a press release with the following
conclusion: “Serious defects in the design and methodology of a
paper by Séralini et al. mean it does not meet acceptable scientific
standards and there is no need to re-examine previous safety
evaluations of genetically modified maize NK603.”   Per
Bergman, who led EFSA’s work, said: “EFSA’s analysis has shown
that deficiencies in the Séralini et al. paper mean it is of
insufficient scientific quality for risk assessment. We believe the
completion of this evaluation process has brought clarity to the
issue.” 
[13] Nothing
could have been farther from the truth.

At
the very minimum, the precautionary principle in instances involving
even the potential for grave damage to the human population would
mandate that the EU Commission and its EFSA should order immediate
further serious, independent long-term studies to prove or disprove
the results of the Seralini tests. That refusal to re-examine its
earlier decision to approve Monsanto GMO maize, no matter what flaws
might or might not have been in the Seralini study, suggested the
EFSA might be trying to cover for the GMO agrichemical lobby at the
very least.

Instead
of clarity, the EFSA statement once more fed EFSA critics who had
long argued that the scientists on EFSA’s GMO Panel had blatant
conflicts of interest with the very GMO lobby they were supposed to
regulate. Corporate Europe Observer, an independent EU corporate
watchdog group noted about the EFSA response, “EFSA failed to
properly and transparently appoint a panel of scientists beyond any
suspicion of conflict of interests; and it failed to appreciate that
meeting with Europe’s largest biotech industry lobby group to discuss
GMO risk assessment guidelines in the very middle of a EU review
undermines its credibility.” 
[14]

More
damaging for the shoddy EFSA coverup on behalf of Monsanto was the
fact that over half of the scientists involved in the GMO panel which
positively reviewed the Monsanto’s study for GMO maize in 2009,
leading to its EU-wide authorization, had conflicts of interests with
the biotech industry.
[15]

A
report by Corporate Europe Observatory (CEO) found that more than
half of the GMO panel experts who signed the approval had conflicts
of interest.

The
conflicts ranged from receiving research funding from the biotech
industry, being a member or collaborator in a pro-biotech industry
association, to writing or reviewing industry-sponsored publications.
Some conflicts revealed a conflict of scientific interests, with some
panel members involved in working on the creation of transgenic
plants – including potatoes – with antibiotic-resistant marker
genes – including nptII.
[16]

Secondly,
although none of EFSA’s GMO panel members were medical experts in
the use of antibiotics in human medicine, they decided that neomycin
and kanamycin were antibiotics with “no or only minor therapeutic
relevance”. The World Health Organisation (WHO) classified these
antibiotics as “critically important” in 2005.

Dutch
scientist Harry Kuiper, chair of the EFSA GMO panel who had close
links to the biotech industry, played a key role in the framing of
this disputed key scientific advice.

Kuiper
himself was an open advocate of less controls on GMO seed
proliferation in the EU. He led the EFSA GMO panel since 2003, during
which time EFSA went from no GMO approvals to 38 GMO seeds approved
for human consumption. The criteria for approval were developed by
Kuiper for EFSA in cooperation with Monsanto and the GMO industry and
a Monsanto pseudo-scientific front group called ILSI, the
Washington-based International Life Sciences Institute, between 2001
and 2003. The board of the noble-sounding ILSI in 2011 was comprised
of senior people from Monsanto, ADM (one of the world’s biggest
purveyors of GMO soybeans and corn), Coca-Cola, Kraft Foods (major
proponent of GMO in foods) and Nestle, another giant GMO food
industry user. 
[17]

One
critic of the blatant conflict of interest in EFSA regulator in bed
with the industry whose practices he was mandated to objectively
assess noted, “During that period, Harry Kuiper and Gijes Kleter
(both members of the EFSA GMO Panel) were active within the ILSI Task
Force as experts and as authors of the relevant scientific
publications. It is a scandal that Kuiper has remained as Chair of
EFSA’s GMO Panel since 2003, and that he is still Chair in spite of
the massive criticism directed at the Panel from NGOs and even from
the Commission and EU member states.” 
[18]

The
brazen conflicts of interest between Monsanto and the agribusiness
lobby and the EFSA went further. In May 2012 Professor Diána Bánáti
was forced to resign as Chairman of the EFSA Management Board when it
was learned she planned to take up a professional position at the
Monsanto-backed International Life Sciences Institute (ILSI) in
Washington. The same Diána Bánáti had been forced to resign, not
as EFSA chairman but as a simultaneous Board Member of ILSI in 2010.
Public interest groups made calls for her to resign from EFSA but to
no avail. 
[19] At
ILSI

she
would be able to use expertise and contacts gained from working for
the EFSA to help GMO companies like Monsanto and other food industry
companies influence policy across the world.

In
sum, it came as no surprise to those familiar with the notorious
“revolving door” in Brussels between the GMO industry and the
regulatory body entrusted with making independent decisions on the
risks of GMO in the EU, that EFSA condemned the Seralini study
results. Most telling however of the brazen pro-GMO industry bias of
EFSA’s GMO Panel members was the fact that the final ruling
statement by the EFSA GMO Panel reviewing Seralini’s results
announced, “Serious defects in the design and methodology of a
paper by Séralini et al. mean it does not meet acceptable scientific
standards and there is no need to re-examine previous safety
evaluations of genetically modified maize NK603.” 
[20]

The
EFSA was not the only source of blatant and reckless pro-GMO
sentiment in Brussels. Some weeks before release of the embarrassing
Seralini study, Anne Glover, chief scientific adviser of the EU
Commission, said in an interview on 24 July, 2012, “There is no
substantiated case of any adverse impact on human health, animal
health or environmental health, so that’s pretty robust evidence,
and I would be confident in saying that there is no more risk in
eating GMO food than eating conventionally farmed food.” She
added that the precautionary principle also “no longer applies,”
which means the EU should not err on the side of caution on the
approval of GMOs—equivalent of a “damn the torpedoes, full speed
ahead with GMO” stance despite polls showing some 60% to 80% of EU
citizens opposed to GMO.
[21]

Were
there any pretense of scientific responsibility in the clearly
corrupt EFSA panel, or Professor Glover’s office, they would have
immediately called for multiple, independent similar long-term rat
studies to confirm or disprove the Seralini results. They and the
Monsanto GMO lobby influencing them clearly had no desire to do
anything but try to slander the Seralini group with vague accusations
and hope the obedient international media would take the headline and
close the embarrassing story. It was typical of the entire history of
the spread of patented GMO seeds and paired toxic herbicides like
Roundup.

Pushing
GMO on Africans

Some
years before the EFSA scandalous ruling, Monsanto had launched a
major project to push its patented GMO seeds and chemicals on unwary
or corruptible African governments. It was called the Alliance for a
Green Revolution in Africa (AGRA). The Rockefeller and Bill Gates
foundations backing the scheme managed to get former UN Secretary
General Kofi Annan, a man with a known bent to corruption, to become
the head of the AGRA.
[22] A
black African was reportedly chosen to overcome criticism among
African states that AGRA was a white man’s neo-colonial effort. It
was, but now with a face from a black African.

In
2006, the Rockefeller Foundation put up $50 million of initial
funding toward the project and the Gates Foundation put up $150
million, the largest single grant of the Gates foundation worldwide
that year. The stated focus of AGRA was to increase crop production,
which involved the same harmful industrialized farming practices
including heavy pesticide use, planting of GMO crops, and training of
African scientists and farmers to spread that model throughout the
continent.

AGRA,
as it called itself, was an alliance again with the same Rockefeller
Foundation which created the “Gene Revolution.” A look at the
AGRA Board of Directors confirmed the fact. In addition to former UN
Secretary General Kofi Annan as chairman, the board numbered almost
exclusively people from the Rockefeller or Gates foundations such as
South African, Strive Masiyiwa, a Trustee of the Rockefeller
Foundation, Sylvia M. Mathews of the Bill & Melinda Gates
Foundation; Rajiv J. Shah of the Gates Foundation; Nadya K.
Shmavonian of the Rockefeller Foundation; Roy Steiner of the Gates
Foundation; Gary Toenniessen the Managing Director of the Rockefeller
Foundation and Akinwumi Adesina, Associate Director, Rockefeller
Foundation.

The
new Africa Green Revolution was clearly a high priority of the
Rockefeller Foundation. 
[23]How
that fit the decades-long eugenics strategy of the same Rockefeller
Foundation will become clearer during the course of this book.

While
they tried hard to keep a low profile, Monsanto and the major GMO
agribusiness giants were accused by researchers of using AGRA to
spread their patented GMO seeds across Africa under the deceptive
label, ‘bio-technology,’ the new euphemism for genetically
engineered patented seeds. To date South Africa was the only African
country permitting legal planting of GMO crops. In 2003 Burkina Faso
authorized GMO trials. In 2005 Kofi Annan’s Ghana drafted
bio-safety legislation and key officials expressed their intentions
to pursue research into GMO crops.

Africa
was the next target after the EU in a US-government campaign to
spread GMO worldwide. Its rich soils made it an ideal candidate. Not
surprisingly many African governments suspected the worst from the
GMO sponsors as a multitude of genetic engineering and biosafety
projects had been initiated in Africa, with the aim of introducing
GMOs into Africa’s agricultural systems. They included sponsorships
offered by the US government to train African scientists in genetic
engineering in the US, biosafety projects funded by the United States
Agency for International Development (USAID) and the World Bank; GMO
research involving African indigenous food crops.

The
Rockefeller Foundation had been working for years to promote, largely
without success, projects to introduce GMOs into the fields of
Africa. They backed research that supports the applicability of GMO
cotton in the Makhathini Flats in South Africa.

Green
Revolution?

The
decision by the Rockefeller Foundation to name their project Alliance
for a Green Revolution in Africa was both calculated Public Relations
and revealing. The original mis-named Green Revolution, developing
hybrid sorts of dwarf wheat in Mexico and later India during the
1960’s had also been a Rockefeller Foundation project. Norman
Borlaug came from his post as a research scientist with the
Rockefeller University to Mexico to develop his wheat varieties. For
the Rockefeller’s the original Green Revolution was an attempt to
organize a global agribusiness monopoly structure based on their
experience with oil. Along with Borlaug’s wonder wheat strains came
large-scale mechanization of the land in Mexico, introduction of
chemical fertilizers and pesticides and a linking of Mexican
agriculture with a global grain market controlled by Archer Daniels
Midland, Cargill and other grain cartel giants close to the
Rockefellers. 
[24]

Now
the same Rockefeller circles wanted to globalize into their worldwide
agribusiness food chain the incredibly rich land and food potentials
of Africa and use the project to spread their patented GMO seeds via
the back door. AGRA was being used to create networks of
“agro-dealers” across Africa, at first with no mention of GMO
seeds or herbicides, in order to have the infrastructure in place to
massively introduce GMO later.
[25]

Monsanto,
which had a strong foothold in South Africa’s seed industry, both
GMO and hybrid, conceived of an ingenious smallholders’ program
known as the ‘Seeds of Hope’ Campaign, introducing a green
revolution package to small scale poor farmers, followed, of course,
by Monsanto’s patented GMO seeds.  Syngenta AG of Switzerland,
one of the ‘Four Horsemen of the GMO Apocalypse’ was pouring
millions of dollars into a new greenhouse facility in Nairobi, to
develop GMO insect resistant maize. 
[26]

The
collusion of the Gates Foundation with Monsanto Corporation was no
accident. The Bill and Melinda Gates Foundation itself was one of the
largest owners of stock shares in Monsanto and AGRA itself also
purchased 500,000 stock shares in Monsanto stocks, proof of that
close relationship. 
[27] 

Despite
many words by Gates officials since the inception of the AGRA agenda
denying that GMO seeds would be used as part of AGRA, their close
relationship with Monsanto had been uncovered as a key element in
their agronomic “new green revolution” strategy, more
appropriately called Alliance for a GMO Revolution in Africa. The
Gates Foundation gave at least $264 million as of 2011 in grants to
AGRA and hired Dr. Robert Horsch, a former Monsanto executive who
developed Roundup, to head up AGRA.
[28]

Gates
Family Eugenics Agenda

Bill
Gates and his Gates Foundation, contrary to their well-cultivated
public image as philanthropic, had an evident and clear eugenics
agenda for Africa, and it evidently included a large role for
Monsanto’s patented seeds.

Gates,
along with billionaire banker David Rockefeller and a handful of
other billionaires created something they called the “Good Club”
at the home of the President of the Rockefeller University in New
York in May 2009. Its aim, according to press reports was to impose a
global series of programs to reduce population—in other words
eugenics.
[29] 

Moreover,
the chairman of the Bill and Melinda Gates Foundation, Bill’s
father, William H. Gates Sr., had been head of the
Rockefeller-financed eugenics group Planned Parenthood, an
organization spawned from the American Eugenics Society.
[30]

In
a 2010 Long Beach California TED conference, Bill Gates himself spoke
enthusiastically of new vaccines that would reduce the planet’s
birth rate. In his titled, “Innovating to Zero!,” along with his
scientifically absurd proposition of reducing manmade CO2 emissions
worldwide to zero by 2050, approximately four and a half minutes into
the talk, Gates declared, ‘First we got population. The world today
has 6.8 billion people. That’s headed up to about 9 billion. Now if
we do a really great job on new vaccines, health care, reproductive
health services, we lower that by perhaps 10 or 15 percent.’ 
[31]

As
one critic described the Monsanto and Gates focus on Africa through
AGRA, “African governments are much weaker and easier to persuade
than the governments of Europe to allow for GMO crops to be
introduced into their countries. Public awareness of the threats of
GMOs has been slower to develop in Africa, and the democratic
processes of citizen advocacy weaker.” 
[32]

Africa
was also the focus for a great global land grab by private companies
from the USA to China in search of some of the planet’s richest
fertile soil. It has been estimated that were proper farming
techniques using purely organic methods, without chemicals introduced
across Africa the Continent could feed ten billion people. Were
Africa to fall to the spread of patented GMO seeds as USA and
Argentina had done, the powerful interests behind the creation of GMO
would have reached a major advance in their global agenda to control
the seeds of life on the planet.

Patrick
Mulvany the head of a UK watchdog organization, UK Food Group, 
identified the strong interest of Monsanto and US-dominated
agribusiness in Africa: “Agribusiness corporations see smallholder
farmers of the developing world as only representing an opportunity
for securing supplies of food at relatively cheap prices, using cheap
labor and, most importantly, as representing a burgeoning market for
proprietary agrochemicals, compliant GMO seeds and fertilisers.”
Mulvany added, “There are opportunities for smallholders to
sustain a strong and vibrant bio-diverse food system using
agro-ecological approaches … yet the only value for agribusiness
are the chains which bind the food serfs to the food barons.”
[33]

Monsanto’s
‘Terminator’ Project

The
United States Government had been financing research since 1983 on a
genetic engineering technology which, when commercialized, would give
its owners the power to control the food seed of entire nations or
regions. Research grants from the US Department of Agriculture went
to a tiny company in Mississippi, Delta & Pine Land. In 2007
Monsanto completed a successful takeover of Delta and Pine Land in a
move that confirmed there was truly a darker agenda behind Monsanto’s
GMO engagement than “feeding the world’s hungry.”

The
takeover of the small Mississippi company in 2007 by Monsanto was
significant because Delta and Pine Land, together with the US
Government, jointly held the patent on what popularly was called
“Terminator” technology, or by its scientific name, Genetic Use
Restriction Technology (GURT).

For
almost a quarter century, since 1983, the US Government had quietly
been working to perfect a genetically engineered technique whereby
farmers would be forced to turn to their seed supplier each harvest
to get new seeds. The seeds would only produce one harvest. After
that the seeds from that harvest would commit ‘suicide’ and be
unusable—a high-tech new serfdom.

The
patented Monsanto ‘suicide’ seeds, officially termed GURTs
(Genetic Use Restriction Technologies), represented an unprecedented
threat to poor farmers in developing countries like India, Nigeria or
Brazil, who traditionally saved their own seeds for the next
planting. In fact, GURTs, more popularly referred to as Terminator
seeds for the brutal manner in which they kill off plant reproduction
possibilities, was a threat to the food security as well of North
America, Western Europe, Japan and anywhere Monsanto and its elite
cartel of GMO agribusiness partners enters a market.

In
March 1998 the US Patent Office granted Patent No. 5,723,765 to Delta
& Pine Land for a patent titled, Control of Plant Gene
Expression. The patent was owned jointly, according to Delta & 
Pine’s Security & Exchange Commission 10K filing, ‘by D&PL
and the United States of America, as represented by the Secretary of
Agriculture.’ To quote further from the official D&PL SEC
filing, ‘The patent broadly covers all species of plant and seed,
both transgenic (GMO-ed) and conventional, for a system designed to
allow control of progeny seed viability without harming the
crop’(sic).’ 
[34]

D&PL
claimed, ‘One application of the technology could be to control
unauthorized planting of seed of proprietary varieties…by making
such a practice non-economic since non-authorized saved seed will not
germinate, and, therefore, would be useless for planting.’ D&PL
calls the thousand-year-old tradition of farmer-saved seed by the
pejorative term, ‘brown bagging’ as though it is something dirty
and corrupt.

Translated
into lay language, D&PL  declared the purpose of its Patent
No. 5,723,765, Control of Plant Gene Expression, was to prevent
farmers who once get trapped into buying GMO seeds from Monsanto from
‘brown bagging’ or being able to break free of control of their
future crops by Monsanto and friends. As D&PL puts it, their
patent gives them ‘the prospect of opening significant worldwide
seed markets to the sale of transgenic (GMO-w.e.) technology in
varietal crops in which crop seed currently is saved and used in
subsequent seasons as planting seed.’
[35]

Terminator
was the answer to the agribusiness dream of controlling world food
production. No longer would Monsanto need to hire expensive
detectives to spy on whether farmers were re-using Monsanto or other
GMO patented seed. Terminator corn or soybeans or cotton seeds could
be genetically modified to ‘commit suicide’ after one harvest
season. The technology would be a means of enforcing Monsanto or
other GMO patent rights, and forcing payment of farmer use fees not
only in developing economies, where patent rights were,
understandably, little respected, but also in industrial OECD
countries.

With
Terminator patent rights, once a country such as Argentina or Brazil
or Iraq or the USA or Canada opened its doors to the spread of GMO
patented seeds among its farmers, their food security would be
hostage to a private multinational company which, for whatever
reasons, especially given its intimate ties to the US Government,
might decide to use ‘food as a weapon’ to compel a US-friendly
policy from that country or group of countries.

If
it sounded implausible that the US Government would back such a
private and dangerous seed technology, one needed only go back to
what Secretary of State Henry Kissinger did in countries like
Allende’s Chile to force a regime change to a ‘US-friendly’
Pinochet dictatorship by withholding USAID and private food exports
to Chile. Kissinger dubbed it ‘food as a weapon.’ Terminator was
merely the logical next step in food weapon technology.

The
role of the US Government in backing and financing Delta & Pine
Land’s decades of Terminator research is even more revealing. As
Kissinger said back in the 1970’s, ‘Control the oil and you can
control entire Continents. Control food and you control people…’

In
a June 1998 interview, USDA spokesman, Willard Phelps, defined the US
Government policy on Terminator seeds. He explained that USDA wanted
the technology to be ‘widely licensed and made expeditiously
available to many seed companies.’ He meant agribusiness GMO giants
like Monsanto, DuPont or Dow. The USDA was open about their reasons:
They wanted to get Terminator seeds into the developing world where
the Rockefeller Foundation had made eventual proliferation of
genetically engineered crops the heart of its GMO strategy from the
beginnings of its rice genome project in 1984.

USDA’s
Phelps stated that the US Government’s goal in fostering the widest
possible development of Terminator technology was ‘to increase the
value of proprietary seed owned by US seed companies and to open up
new markets in Second and Third World countries.’ 
[36]

Under
WTO rules on free trade in agriculture, countries are forbidden to
impose their own national health restrictions on GMO imports if it is
deemed to be an ‘unfair trade barrier.’ It begins to become clear
why it was the US Government and US agribusiness which during the
late 1980’s pushed at the GATT Uruguay Round for creation of a
World Trade Organization, with its supranational arbitrary powers
over world agriculture trade. It all fits into a neat picture of
patented seeds, forced on reluctant WTO member nations, under threat
of WTO sanctions, and now of Terminator or suicide seeds.

Monsanto
Terminator deception

What
was so attractive about Delta & Pine Land that Monsanto made a
second bid to add it to its global genetically-engineered seeds
empire?

It
was the patent that Delta & Pine Land, together with the US
Government, held Patent No. 5,723,765, titled, Control of Plant Gene
Expression. The USDA through its Agricultural Research Service
(USDA-ARS) worked with Delta & Pine Land since 1983 to perfect
Terminator GMO technology. Patent No. 5,723,765 was the patent for
Terminator technology.

In
early 1999 Monsanto, the largest producer of GMO seeds and related
agri-chemicals, announced it was acquiring Delta & Pine Land
along with Delta’s Terminator patents.

In
October 1999, however, following a worldwide storm of protest against
Terminator seeds that threatened the very future of the Rockefeller
Foundation’s ‘Gene Revolution’ Dr. Gordon Conway, President of
the Rockefeller Foundation, met privately with the Board of Directors
of Monsanto. Conway convinced Monsanto that for the long-term future
of their GMO Project, they must go public to indicate to a worried
world that it would not ‘commercialize’ Terminator.

The
Anglo-Swiss Syngenta joined with Monsanto in declaring solemnly that
they would also not “commercialize” their work on GURTS or
Terminator suicide seed technology.

That
1999 announcement took enormous pressure off of Monsanto and the
agribusiness GMO giants, allowing them to advance the proliferation
of their patented GMO seeds globally. Terminator would come later,
once farmers and entire national agriculture areas like North America
or Argentina or India had been taken over by GMO crops. Then, of
course, it would be too late. Despite the Monsanto declaration of a
moratorium on Terminator development, the US Government and Delta &
Pine Land refused to drop their Terminator development.

In
2000, a year after the Monsanto Terminator moratorium announcement,
the Clinton Administration’s USDA Secretary, Dan Glickman, refused
repeated efforts by various agriculture and NGO organizations to drop
the Government’s support for Terminator or GURTs. His Department’s
excuse for not dropping support for the work with Delta & Pine
Land was that it allowed the US Government to put ‘leverage’ on
D&PL to ‘protect the public interest.’

Delta
Vice President, Harry Collins, declared at the time in a press
interview in the Agra/Industrial Biotechnology Legal Letter, ‘We’ve
continued right on with work on the Technology Protection System (TPS
or Terminator). We never really slowed down. We’re on target,
moving ahead to commercialize it. We never really backed off.’ 
[37]

Nor
did their partner, the United States Department of Agriculture, back
down on Terminator after 1999. In 2001 the USDA Agricultural Research
Service (ARS) website announced: ‘USDA has no plans to introduce
TPS into any germplasm…Our involvement has been to help develop the
technology, not to assist companies to use it.’ They went on to say
the USDA was, ‘committed to making the [Terminator] technology as
widely available as possible, so that its benefits will accrue to all
segments of society (sic)…ARS intends to do research on other
applications of this unique gene control discovery…When new
applications are at the appropriate stage of development, this
technology will also be transferred to the private sector for
commercial application.’
[38]

In
2001, the USDA and Delta & Pine executed a Commercialization
Agreement for Terminator, its infamous Patent No. 5,723,765. The
Government and Delta & Pine Land were not at all concerned about
worldwide outcry against Terminator.

The
key scientific member of the Delta & Pine Land board since 1993,
Dr. Nam-Hai Chua was also head of the Rockefeller University Plant
Molecular Biology Laboratory in New York, and had been for over 25
years, the labs which are at the heart of the Rockefeller
Foundation’s decades-long development, and spending of more than
$100 millions of its own research grants to create their GMO
Revolution. Until 1995, Chua was also a scientific consultant to
Monsanto Corporation, as well as to DuPont’s Pioneer Hi-Bred
International. Chua was at the heart of Rockefeller’s Gene
Revolution. And their development of Terminator was in the center of
that work. 
[39]

This
vast global network combined with Monsanto’s dominant position in
the GMO seeds and agri-chemicals market along with the unique DP&L 
Patent No. 5,723,765, Control of Plant Gene Expression, now gave
Monsanto and its close friends in Washington an enormous advance in
their plans to dominate world food and plant seed use. It was an
ominous goal and the US Government implemented it ruthlessly as the
2003 military occupation of Iraq was to prove.
[40]


[1] Seralini
et al., Op. Cit.

[2] Ibid. 

[3] Ibid.

[4] Ibid.

[5] Gilles-Eric
Seralini et al, 
Genetically
modified crops safety assessments: present limits and possible
improvements
,
Environmental Sciences Europe 2011, 23:10, accessed
in
http://www.enveurope.com/content/23/1/10.

[6] Ibid.

[7] Aris,
A., Leblanc, S., 
Maternal
and fetal exposure to pesticides associated to genetically modified
foods in Eastern Townships of Quebec, Canada
,
Reproductive Toxicology, 2011 May;31(4):528-33. Epub 2011 Feb 18.

[8] European
Food Safety Authority (EFSA),
 Scientific
Opinion of the Panel on Genetically Modified Organisms on
applications (EFSA-GMO-NL-2005-22 and EFSA-GMO-RX-NK603) for the
placing on the market of the genetically modified glyphosate
tolerant maize NK603 for cultivation, food and feed uses and import
and processing, and for renewal of the authorisation of maize NK603
as existing product, 
The
EFSA Journal (2009) 1137, 1-50.

[9] Ibid.

[10] Ibid.

[11] GMO-Kompass, Food
Safety Evaluation–Evaluating Safety: A Major Undertaking
,
February 15, 2006, accessed
in 
http://www.gmo-compass.org/eng/safety/human_health/41.evaluation_safety_gm_food_major_undertaking.html

[12] Ibid.

[13] EFSA, Séralini
et al. study conclusions not supported by data, says EU risk
assessment community
,
EFSA Press Release, 28 November 2012, accessed
in
http://www.efsa.europa.eu/en/press/news/121128.htm

[14] Corporate
Europe Observatory, Op. Cit.

[15] Ibid.

[16] Corporate
Europe Observatory,  
Approving
the GM potato: conflicts of interest, flawed science and fierce
lobbying
,
CorporateEurope.org, November 7, 2011, accessed
in
http://corporateeurope.org/publications/approving-gm-potato-conflicts-in…

[17] ILSI, 2011
Annual Report, Board of Trustees
,
accessed in 
http://www.ilsi.org/Documents/ILSI_AR2011_rFinal.pdf

[18] Tore
B. Krudtaa, 
Harry
Kuiper Chair of EFSA GMO panel – Another regulator in the business
of deregulation?
,
Monsanto.No, 22 September 2011, accessed
in
http://www.monsanto.no/index.php/en/environment/gmo/gmo-news/166-harry-kuiper-chair-of-efsa-gmo-panel-another-regulator-in-the-business-of-deregulation

[19] EFSA, FAQ
on the resignation of Diana Banati as member and Chair of EFSA´s
Management Board
,
accessed
in  
http://www.efsa.europa.eu/en/faqs/faqresignationdianabanati.htm

[20] EFSA, Séralini
et al. study conclusions not supported by data, says EU risk
assessment community
,
EFSA Press Release, 28 November 2012, accessed
in
http://www.efsa.europa.eu/en/press/news/121128.htm.

[21] EurAktiv.com, GMOs:
“Anne Glover, you are wrong,”
 27
July 2012, accessed
in
http://www.euractiv.com/cap/gmos-anne-glover-wrong-analysis-514185

[22] Ethics
Scoreboard,
 Kofi
Annan and the U.N.’s Culture of Corruption
,
5 March 2005, accessed
in 
http://www.ethicsscoreboard.com/list/annan.html

[23] Ibid.

[24] Cf.
Kapitel 9, pp. 172-187.

[26] Ibid.

[27] La
Via Campesina, 
Global
Small Farmers Denounce Gates Foundation Purchase of 500,000 Monsanto
Stock Shares
,
September 13, 2010, accessed
in
http://www.organicconsumers.org/articles/article_21606.cfm

[28] Ibid.

[29] F.
William Engdahl, 
Secret
Good Club holds first meeting in New York
,
2 June  2009.

[30] PBS, Transcript
Bill Moyers Interviews Bill Gates
,
May 9, 2003, accessed in

http://www.pbs.org/now/transcript/transcript_gates.html.

[31] F.
William Engdahl, 
Bill
Gates talks about ‘vaccines to reduce population,

4 March 2010, accessed
in 
http://oilgeopolitics.net/Swine_Flu/Gates_Vaccines/gates_vaccines.html.

[32] Stephen
Bartlett, 
Wikileaks
Documents Gov Complicity with GMO Seed Monopolies
,
Netline, January 2011, accessed
in  
http://www.agriculturalmissions.org/netline_2011_002.htm.

[33] Matthew
Newsome, 
Does
the future of farming in Africa lie in the private sector?,
 23
November 2012, 
guardian.co.uk,
Sponsored by the Bill and Melinda Gates Foundation, accessed
in 
http://www.guardian.co.uk/global-development/poverty-matters/2012/nov/23/future-farming-africa-private-sector.

[34] F.
William Engdahl,
 Monsanto
buys ‘Terminator’ Seeds Company

August 27, 2006, accessed
in 
http://www.engdahl.oilgeopolitics.net/GMO/Monsanto/monsanto.html

[35] Ibid.

[36] Ibid.

[37] Ibid.

[38] Ibid.

[39] Ibid.

Hier het boek dat Engdahl over deze zaak schreef:

Image

You can find this great and informative book on amazon.com 

 www.williamengdahl.com

========================

Zie ook: ‘Obama, ‘kampioen natuur en milieu’ tekent lobbydocument Monsanto……..

        en: ‘Bayer/Monsanto: de vergiftiging van de aarde. Hoe kunnen fabrikanten van pesticiden en transgene zaden nog rustig slapen…..??

        en: ‘Glyfosaat, een kankerverwekkend gif, nu ook gevonden in honing en graan……..

        en: ‘Voedselfraude in de VS >> als het aan de EU ligt binnenkort ook in onze supermarkten……

        en:  ‘Bayer oefent druk uit op Nederland voor nieuw ‘bijengif…….’

        en: ‘TTIP: wat ons te wachten staat >> verboden labeling van o.a. genetisch gemanipuleerde voeding……

       en: ‘Van Dam (PvdA staatssecretaris), Monsanto lobbyist….. EU tekent waarschijnlijk voor nog 7 jaar lang vergiftiging mens en dier met glyfosaat………

       en: ‘Monsanto ‘liefdadigheidsorganisatie die zich inzet voor wereldvoedselprobleem……

       en: ‘Monsanto en EPA hebben samen Roundup veilig verklaart >> Alweer een ‘samenzweringstheorie’ verheven tot waarheid

       en: ‘Timmermans’ Europese Commissie dreigt in strijd met de regels het kankerverwekkend glyfosaat, opnieuw toe te laten op de EU markt………….

       en: ‘EU: verbiedt het uiterst gevaarlijke glyfosaat voorgoed!‘ (Helaas, te vroeg gejuicht…)

       en: ‘Kamp (VVD) glyfosaat gifmenger van het jaar!

       en: ‘Glyfosaat, de leugens van Monsanto over dit kankerverwekkend gif……….

       en: ‘Bas Eickhout (‘GroenLinks’ EU): het is nodig dat glyfosaat nog 5 jaar gebruikt mag worden……… ha! ha! ha! ha! ha! ha! ha!

       en: ‘Op aardbei zes keer meer landbouwgif dan op ander fruit………

       en: ‘EPA tegenstrijdig over glyfosaat >> EU ‘politici’ laten als ware lobbyisten van o.a. gifmenger Monsanto het kankerverwekkende Roundup nog eens 5 jaar op ons los….

       en: ‘Greenpeace vraagt Australische regering de verkoop van Roundup aan banden te leggen, nadat een VS rechter oordeelde dat het gif kankerverwekkend is…..

Zie daarnaast ook: Verbied gebruik glyfosaat tot er bewijzen zijn (De Standaard)http://www.standaard.be/cnt/dmf20170426_02852617 en: Monsanto koopt wetenschap die de “onschuld” van glyfosaat bewijst.http://www.dewereldmorgen.be/artikel/2017/03/27/monsanto-koopt-wetenschap-die-de-onschuld-van-glyfosaat-bewijst