Showing posts with label Vaccines. Show all posts
Showing posts with label Vaccines. Show all posts
Thursday, October 7, 2010
Friday, October 1, 2010
Bill Gates says vaccines can help reduce world population
(NaturalNews) In a recent TED conference presentation, Microsoft billionaire Bill Gates, who has donated hundreds of millions of dollars to new vaccine efforts, speaks on the issue of CO2 emissions and its effects on climate change. He presents a formula for tracking CO2 emissions as follows: CO2 = P x S x E x C.
P = People
S = Services per person
E = Energy per service
C = CO2 per energy unit
Then he adds that in order to get CO2 to zero, "probably one of these numbers is going to have to get pretty close to zero."
Following that, Bill Gates begins to describe how the first number -- P (for People) -- might be reduced. He says: "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 could lower that by perhaps 10 or 15 percent."
You can watch this yourself at:
http://www.naturalnews.tv/v.asp?v=A...
Reducing the world population through vaccines
This statement by Bill Gates was not made with any hesitation, stuttering or other indication that it might have been a mistake. It appears to have been a deliberate, calculated part of a well developed and coherent presentation.So what does it mean when Bill Gates says "if we do a really great job on new vaccines... we could lower [world population] by 10 or 15 percent?"
Clearly, this statement implies that vaccines are a method of population reduction. So is "health care," which all NaturalNews readers already know to be more of a "sick care" system that actually harms more people than it helps.
Perhaps that's the whole point of it. Given that vaccines technology help almost no one from a scientific point of view (http://www.naturalnews.com/029641_v...), it raises the question: For what purpose are vaccines being so heavily pushed in the first place?
Bill Gates seems to be saying that one of the primary purposes is to reduce the global population as a mechanism by which we can reduce CO2 emissions. Once again, watch the video yourself to hear him say it in his own words:
http://www.naturalnews.tv/v.asp?v=A...
How can vaccines actually be used to reduce world population?
Let's conduct a mental experiment on this issue. If vaccines are to be used to reduce world population, they obviously need to be accepted by the majority of the people. Otherwise the population reduction effort wouldn't be very effective.And in order for them to be accepted by the majority of the people, they obviously can't just kill people outright. If everybody started dropping dead within 24 hours of receiving the flu shot, the danger of vaccines would become obvious rather quickly and the vaccines would be recalled.
Thus, if vaccines are to be used as an effective population reduction effort, there are really only three ways in which they might theoretically be "effective" from the point of view of those who wish to reduce world population:
#1) They might kill people slowly in a way that's unnoticeable, taking effect over perhaps 10 - 30 years by accelerating degenerative diseases.
#2) They might reduce fertility and therefore dramatically lower birth rates around the world, thereby reducing the world population over successive generations. This "soft kill" method might seem more acceptable to scientists who want to see the world population fall but don't quite have the stomach to outright kill people with conventional medicine. There is already evidence that vaccines may promote miscarriages (http://www.naturalnews.com/027512_v...).
#3) They might increase the death rate from a future pandemic. Theoretically, widespread vaccination efforts could be followed by a deliberate release of a highly virulent flu strain with a high fatality rate. This "bioweapon" approach could kill millions of people whose immune systems have been weakened by previous vaccine injections.
This is a known side effect of some vaccines, by the way. A study documenting this was published in PLoS. Read the story here: http://www.naturalnews.com/028538_s...
Here's the study title and citation: Does Seasonal Influenza Vaccination Increase the Risk of Illness with the 2009 A/H1N1 Pandemic Virus?
Viboud C, Simonsen L (2010) Does Seasonal Influenza Vaccination Increase the Risk of Illness with the 2009 A/H1N1 Pandemic Virus? PLoS Med 7(4): e1000259. doi:10.1371/journal.pmed.1000259
The short answer is yes, seasonal flu vaccines do cause increased susceptibility to the H1N1 pandemic virus. In other words, seasonal flu vaccines could set up the population for a "hard kill" pandemic that could wipe out a significant portion of the global population (perhaps 10 to 15 percent, as Bill Gates suggested).
Conveniently, their deaths could be blamed on the pandemic, thereby diverting blame from those who were really responsible for the plot. As yet another beneficial side effect for the global population killers, the widespread deaths could be used as a fear tool to urge more people to get vaccinated yet again, and the entire cycle could be repeated until world population was brought down to whatever manageable level was desired... all in the name of health care!
The more people around the world are vaccinated before the release of the "hard kill" pandemic virus, the more powerful the effect of this approach.
The Bill and Melinda Gates Foundation
Perhaps not coincidentally, the Bill and Melinda Gates Foundation has funneled hundreds of millions of dollars into vaccine programs targeting people all over the world. One such program is researching the development of "sweat-triggered vaccines" that could use specially-coated nano-materials to deliver vaccines to people without using injections.More interestingly, his foundation has also invested millions in sterilization technologies that have been called a "temporary castration" solution. (http://www.naturalnews.com/028887_v...)
It seems that the actions of the Gates foundation are entirely consistent with the formula for CO2 reduction that Bill Gates eluded to in his TED conference speech: CO2 = P x S x E x C.
By reducing birth rates (through sterilization technologies) and increasing vaccine penetration throughout the world population (by using sweat-triggered nano-vaccines), his stated goal of reducing the world population by 10 to 15 percent could be reached within just a few years.
Who will be left alive? The smart people
The interesting thing about all this is that this campaign to reduce global population through vaccines will obviously not impact people who consciously avoid vaccines. And those people, by and large, tend to be the more intelligent, capable people who actually have an improved ability to move human civilization forward with thoughtful consideration.I can only imagine that those people designing this vaccine-induced population control measure might be sitting around a table chuckling to themselves and saying, "It's only the stupid people that are going to be killed off anyway, so this is actually helping the future of humankind!" (Their words, not mine.)
In a weird world government kind of way, this effort might actually be based on some distorted vision of philanthropy where some of the most powerful people in the world quite literally believe the way to save humanity is to kill off as many of the gullible people as possible. Vaccines are, in effect, an "evil genius" kind of way to conduct an IQ test on the population at large: If you go get vaccinated every flu season, you're not too bright and probably don't engage the kind of strong mental faculties that humanity will no doubt need if it is to face a future where it is now all but obvious we are not alone in the universe.
If humanity is to save itself from its own destruction and compete as an uplifted species in our universe, killing off the least intelligent members of society (or making them infertile) may appear to the world controllers to be a perfectly reasonable approach. I disagree with that approach, but it may be precisely what they are thinking.
In any case, choosing to receive a seasonal flu shot is undoubtedly an admission that you have failed some sort of universal IQ test, whether or not this is the intention of world influencers such as Bill Gates. More importantly, it is also a betrayal of your own biology, because it indicates you don't believe in the ability of your own immune system to protect you even from mild infections.
Perhaps the world vaccine conspirators figure that if people are willing to betray themselves anyway, it's not much different for governments and institutions to betray them as well. In other words, if you don't even care enough about your own health to take care of your health, why should any government care about protecting your health, either?
As you ponder this, also consider something else: The U.S. is going broke due to sick-care costs which are rising dramatically under the new federal health care reform guidelines. Can you guess the fastest and easiest way to reduce those health care costs? If you guessed, "unleash a hard-kill pandemic that takes out a significant portion of the weak or sick people" then you guessed right. Sadly, killing off those most vulnerable to sickness could save the U.S. government literally billions of dollars in sick-care expenditures. Plus, it would save Social Security yet more billions by avoiding ongoing monthly payouts. (Again, I am completely against such an approach because I value human life, but I also know we live in a world where the people in charge have little or no respect for human life and will readily sacrifice human lives to achieve their aims.)
As far as Bill Gates goes, consider his statement in the context of what we've discussed here: "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 could lower that by perhaps 10 or 15 percent."
It suddenly seems to make a lot of sense when you understand that reducing the population reduces CO2 emissions, and using more vaccines on more people increases the death rate of the population.
My advice? Try to avoid being among those 10 to 15 percent who get culled through global vaccine programs. You will not only save your life, you'll also pass the "universal IQ test" which determines whether you're smart enough to know that injecting your body with chemicals and viral fragments in order to stop "seasonal flu" is a foolish endeavor.
Be healthy and wise, and you'll survive the world depopulation effort that victimizes conventional thinkers who don't have the intelligence to question what they're being told to do by their own corrupt governments
Thursday, September 30, 2010
"Three Articles: Rockefeller Depopulation Plans Exposed"
"Part 1: Rockefeller Foundation Developed Vaccines For “Mass-Scale” Fertility Reduction
In its 1968 yearly report, the Rockefeller Foundation acknowledged funding the development of so-called “anti-fertility vaccines” and their implementation on a mass-scale. From page 51 onward we read:
“(…) several types of drugs are known to diminish male fertility, but those that have been tested have serious problems of toxicity. Very little work is in progress on immunological methods, such as vaccines, to reduce fertility, and much more research is required if a solution is to be found here.”
The possibility of using vaccines to reduce male fertility was something that needed to be investigated further, according to the Rockefeller Foundation, because both the oral pill and the IUD were not suitable for mass-scale distribution:
“We are faced with the danger that within a few years these two “modern” methods, for which such high hopes have been held, will in fact turn out to be impracticable on a mass scale.”
The possibility of administrating hormone preparations to reduce fertility was also mentioned, although- states the report- they have been known to “cause bleeding problems, which may limit their usefulness.”
“A semipermanent or renewable subcutaneous implant of these hormones has been suggested, but whether or not the same difficulties would result has not been determined.”
Saying that research thus-far had been too low-grade to produce any substantial results, the report was adamant:
“The Foundation will endeavour to assist in filling this important gap in several ways:
1- “Seeking out or encouraging the development of, and providing partial support to, a few centres of excellence in universities and research institutions in the United States and abroad in which the methods and points of view of molecular biology are teamed with the more traditional approaches of histology, embryology,and endocrinology in research pertinent to development of fertility control methods;”
2- “Supporting research of individual investigators, oriented toward development of contraceptive methods or of basic information on human reproduction relevant to such developments;”
3- “Encouraging, by making research funds available, as well as by other means, established and beginning investigators to turn their attention to aspects of research in reproductive biology that have implications for human fertility and its control;”
4- “Encouraging more biology and biochemistry students to elect careers in reproductive biology and human fertility control, through support of research and teaching programs in departments of zoology, biology, and biochemistry.”
The list goes on and on. Motivation for these activities, according to the RF?
“There are an estimated five million women among America’s poverty and near-poverty groups who need birth control service (…). The unchecked fertility of the indigent does much to perpetuate poverty, undereducation, and underemployment, not only in urban slums, but also in depressed rural areas.”
It wasn’t long before all the Foundation’s efforts began to have effect. In its annual report of 1988, The RF was happy to report the progress made by the Foundation’s Population Division in the field of anti-fertility vaccines:
“India’s National Institute of Immunology successfully completed in 1988 the first phase of trials with three versions of an anti-fertility vaccine for women. Sponsored by the government of India and supported by the Foundation, the trials established that with each of the tested vaccines, at least one year of protection against pregnancy could be expected, based on the levels of antibodies formed in response to the immunization schedule.”
In its 1997 review of anti-fertility vaccines, Indian based International Centre for Genetic Engineering and Biotechnology didn’t forget to acknowledge its main benefactor:
“The work on LHRH and HCG vaccines was supported by research grants of The Rockefeller Foundation, (…).”
In the 1990s the work on anti-fertility vaccines went in overdrive, especially in third-world nations, as did the funding provided by the deep pockets of the Rockefeller Foundation. At the same time, the target-population of the globalists- women- began to stir uncomfortably with all this out-in-the-open talk of population reduction and vaccines as a means to achieve it.
Betsy Hartman, Director of the Population and Development Program at Hampshire College, Massachusetts and “someone who believes strongly in women’s right to safe, voluntary birth control and abortion”, is no supporter of the anti-fertility vaccine, as brought into being by the Rockefeller Foundation. She explains in her essay Population control in the new world order:
“Although one vaccine has been tested on only 180 women in India, it is being billed there as ‘safe, devoid of any side effects and completely reversible’. The scientific community knows very well that such assertions are false – for instance, many questions still remain about the vaccine’s long-term impact on the immune system and menstrual cycle. There is also evidence on film of women being denied information about the vaccine in clinical trials. Nevertheless, the vaccine is being prepared for large-scale use.”
The Women’s Global Network for Reproductive Rights based in Amsterdam, the Netherlands, quoted “a leading contraceptive researcher as saying:
“Immunological birth control methods will be an ‘antigenic weapon’ against the reproductive process, which left unchecked, threatens to swamp the world.”
Animal rights activist ms. Sonya Ghosh also expressed concerns about the Rockefeller-funded anti-fertility vaccine and its implementation:
“Instead of giving individual women more options to prevent pregnancy and protect against AIDs and sexually transmitted diseases, the anti fertility vaccine is designed to be easily administered to large numbers of women using the least resources. If administered to illiterate populations the issues of user control and informed consent are further cause for concern.”
To avoid such debates, the Foundation has in the last couple of decades consorted to its long-practised and highly successful methods of either outright lying through its teeth or using deceptive language to hide the fact that it continues to work tirelessly toward its long-stated mission. If you think the RF and others have abandoned their anti-fertility efforts with the help of vaccines, think again or read this article.
Part 2: Global Distribution of Rockefeller-Funded Anti-Fertility Vaccine Coordinated by WHO
In addition to the recent PrisonPlanet-exclusive Rockefeller Foundation Developed Vaccines For “Mass-Scale” Fertility Reduction- which outlines the Rockefeller Foundation’s effortsin the 1960s funding research into so-called “anti-fertility vaccines”- another series of documents has surfaced, proving beyond any doubt that the UN Population Fund, World Bank and World Health Organization picked up on it, further developing it under responsibility of a “Task Force on Vaccines for Fertility Regulation”.
Just four years after the Rockefeller Foundation launched massive funding-operations into anti-fertility vaccines, the Task Force was created under auspices of the World Health Organization, World Bank and UN Population Fund. Its mission, according to one of its members, to support:
“basic and clinical research on the development of birth control vaccines directed against the gametes or the preimplantation embryo. These studies have involved the use of advanced procedures in peptide chemistry, hybridoma technology and molecular genetics as well as the evaluation of a number of novel approaches in general vaccinology. As a result of this international, collaborative effort, a prototype anti-HCG vaccine is now undergoing clinical testing, raising the prospect that a totally new family planning method may be available before the end of the current decade.”
In regards to the scope of the Task Force’s jurisdiction, the Biotechnology and Development Monitor reported:
“The Task Force acts as a global coordinating body for anti-fertility vaccine R&D in the various working groups and supports research on different approaches, such as anti-sperm and anti-ovum vaccines and vaccines designed to neutralize the biological functions of hCG. The Task Force has succeeded in developing a prototype of an anti-hCG-vaccine.”
One of the Task Force members, P.D. Griffin, outlined the purpose and trajectory of these Fertility Regulating Vaccines. Griffin:
“The Task Force has continued to coordinate its research activities with other vaccine development programmes within WHO and with other international and national programmes engaged in the development of fertility regulating vaccines.”
Griffin also admitted to the fact that one of the purposes of the vaccines is the implementation in developing countries. Griffin:
“If vaccines could be developed which could safely and effectively inhibit fertility, without producing unacceptable side effects, they would be an attractive addition to the present armamentarium of fertility regulating methods and would be likely to have a significant impact on family planning programmes.”
Also, one of the advantages of the FRVs over “currently available methods of fertility regulation” the Task Force states, is the following (179):
“low manufacturing cost and ease of delivery within existing health services.”
Already in 1978, the WHO’s Task Force (then called Task Force on Immunological Methods for Fertility Regulation) underlined the usefulness of these vaccines in regards to the possibility of “large scale synthesis and manufacture” of the vaccine:
“The potential advantages of an immunological approach to fertility regulation can be summarized as follows: (a) the possibility of infrequent administration, possibly by paramedical personnel; (b) the use of antigens or antigen fragments, which are not pharmacologically active; and (c) in the case of antigens of known chemical structure, there is the possibility of large-scale synthesis and manufacture of vaccine at relatively low cost.”
In 1976, the WHO Expanded Programme of Research, Development and Research Training in Human Reproduction published a report, stating:
“In 1972 the Organization (…) expanded its programme of research in human reproduction to provide an international focus for an intensified effort to improve existing methods of fertility regulation, to develop new methods and to assist national authorities in devising the best ways of providing them on a continuing basis. The programme is closely integrated with other WHO research on the delivery of family planning care by health services, which in turn feeds into WHO’s technical assistance programme to governments at the service level.”
Although the term “Anti-Fertility Vaccine”, coined by the Rockefeller Foundation, was replaced by the more bureaucratic sounding “Fertility Regulating Vaccine (FRV), the programme was obviously the same. Besides, the time-line shows conclusively that the WHO, UN Population Fund and World Bank continued on a path outlined by the Rockefellers in the late 1960s. By extension, it proves that all these organization are perfectly interlocked, best captured under the header “Scientific Dictatorship”. The relationship between the WHO and the Rockefeller Foundation is intense. In the 1986 bulletin of the World Health Organization, this relationship is being described in some detail. While researching the effectiveness of “gossypol” as an “antifertility agent”, the bulletin states:
“The Rockefeller Foundation has supported limited clinical trials in China and smallscale clinical studies in Brazil and Austria. The dose administered in the current Chinese trial has been reduced from 20 mg to 10-15 mg/day during the loading phase in order to see if severe oligospermia rather than consistent azoospermia would be adequate for an acceptable, non-toxic and reversible effect. Meanwhile, both the WHO human reproduction programme and the Rockefeller Foundation are supporting animal studies to better define the mechanism of action of gossypol.”
In August of 1992, a series of meetings was held in Geneva, Switzerland, regarding “fertility regulating vaccines”. According to the document Fertility Regulating Vaccines (classified by the WHO with a limited distribution) present at those meetings were scientists and clinicians from all over the globe, including then biomedical researcher of the American Agency for International development, and current research-chief of USAID, Mr. Jeff Spieler.
In 1986 Mr. Spieler declared:
“A new approach to fertility regulation is the development of vaccines directed against human substances required for reproduction. Potential candidates for immunological interference include reproductive hormones, ovum and sperm antigens, and antigens derived from embryonic or fetal tissue.(…). An antifertility vaccine must be capable of safely and effectively inhibiting a human substance, which would need somehow to be rendered antigenic. A fertility-regulating vaccine, moreover, would have to produce and sustain effective immunity in at least 95% of the vaccinated population, a level of protection rarely achieved even with the most successful viral and bacterial vaccines. But while these challenges looked insuperable just a few years ago, recent advances in biotechnology- particularly in the fields of molecular biology, genetic engineering and monoclonal antibody production- are bringing antifertility vaccines into the realm of the feasible.”
“Vaccines interfering with sperm function and fertilization could be available for human testing by the early 1990s”, Spieler wrote.
In order for widespread use of these vaccines, Spieler writes, the vaccine must conquer “variations in individual responses to immunization with fertility-regulating vaccines”.
“Research”, he goes on to say,”is also needed in the field of “basic vaccinology”, to find the best carrier proteins, adjuvants, vehicles and delivery systems.”
In the 1992 document, the problem of “variations in individual responses” is also discussed:
“Because of the genetic diversity of human populations”, states the document, “immune responses to vaccines often show marked differences from one individual to another in terms of magnitude and duration. These differences may be partly or even completely overcome with appropriately engineered FRVs (Fertility Regulating Vaccines) and by improvements in our understanding of what is required to develop and control the immune response elicited by different vaccines.”
The picture emerging from these facts is clear. The WHO, as a global coordinating body, has since the early 70s continued the development of the Rockefeller-funded “anti-fertility vaccine”. What also is becoming clear, is that extensive research has been done to the delivery systems in which these anti-fertility components can be buried, such as regular anti-viral vaccines. It’s a mass-scale anti-fertilization programme with the aim of reducing the world’s population: a dream long cherished by the global elite.
It seems there is no limit to the Rockefeller Foundation’s ambitions to introduce anti-fertility compounds into either existing “health-services”, such as vaccines, or- as appears to be the case now- average consumer-products.
The 1985 Rockefeller Foundation’s annual reportunderlined its ongoing dedication towards finding good use for the anti-fertility substance “gossypol”, or C30H30O8 – as the description reads.
Indeed, gossypol, a toxic polyphenol derived from the cotton plant, was identified early on in the Foundation’s research as an effective sterilant. The question was, how to implement or integrate the toxic substance into crops.
“Another long-term interest of the Foundation has been gossypol, a compound that has been shown to have an antifertility effect in men, By the end of 1985, the Foundation had made grants totaling approximately $1.6 million in an effort to support and stimulate scientific investigations on the safety and efficacy of gossypol.”
In the 1986 Rockefeller Foundation annual report, the organization admits funding research into the use of fertility-reducing compounds in relation to food for “widespread use”:
“Male contraceptive studies are focused on gossypol, a natural substance extracted from the cotton plant, and identified by Chinese researchers as having an anti-fertility effect on men. Before widespread use can be recommended, further investigation is needed to see if lowering the dosage can eliminate undesirable side-effects without reducing its effectiveness as a contraceptive. The Foundation supported research on gossypol’s safety, reversibility and efficacy in seven different 1986 grants.”
In the RF’s 1988 annual report, gossypol as a contraceptive was also elaborated upon (page 22):
“Gossypol, a natural substance found in the cotton plant, continues to show promise as an oral contraceptive for men. Because it suppresses sperm production without affecting sex hormone levels, it is unique among the experimental approaches to fertility control in men. Foundation-funded scientists worldwide have assembled an aray of information about how gossypol works, and studies continue on a wide variety of its clinical applications. Dose reduction is being investigated to reduce health risks associated with the use of gossypol.”
The following year, according to the annual report, funds were allocated to several research institutions to see how this “dose reduction” could best be accomplished without interfering with the ant-fertility effects of gossypol.
(1988- $ 400,000, in addition to remaining funds from prior year appropriations) To support research on gossypol, its safety, reversibility, and efficacy as a contraceptive for use by men (…).”
Mention is made on money allocated to the University of Texas, “for a study of gossypol’s effects on DNA replication (…).”
The last mention of gossypol in the Foundation’s annals we find in the 1994 annual report, where funds were appropriated to the University of Innsbruck of Austria “for a study at the Institute of Physiology on the molecular action of gossypol at the cellular level.”
It seems that the funded scientists have indeed found a way of “lowering the dosage” of gossypol, circumventing the toxicity of the substance, so as to suppress or even eliminate these “undesirable side-effects”, which include: low blood potassium levels, fatigue, muscle weakness and even paralysis. If these effects could be eliminated without reducing the anti-fertility effects, the Foundation figured, it would be a highly effective and almost undetectable sterilant.
Although overtly, research into and development of gossypol as a anti-fertility compound was abandoned in the late 1990s, the cottonseed containing the substance was especially selected for mass distribution in the beginning of the current decade. Around 2006 a media-campaign was launched, saying the cottonseed could help defeat hunger and poverty.
In 2006, NatureNews reported that RNA interference (or RNAi) was the way to go. On the one hand it would “cut the gossypol content in cottonseeds by 98%, while leaving the chemical defenses of the rest of the plant intact.” Furthermore, the article quoted Dr. Deborah P. Delmer, the Rockefeller Foundation’s associate director of food security, who was quick to bury any concern:
“Deborah Delmer, associate director of the Rockefeller Foundation in New York City and an expert in agricultural food safety, points out that a benefit of using RNAi technology is that it turns off a gene process rather than switching on a novel function. “So instead of introducing a new foreign protein, you’re just shutting down one process,” Delmer says. “In that sense, I think that the safety concerns should be far less than other GM technologies.”
A 2006, National Geographic article Toxin-Free Cottonseed Engineered; Could Feed Millions Study Says, quotes the director of the Laboratory for Crop Transformation (Texas A&M Universtity), Keerti Singh Rathore as saying:
“A gossypol-free cottonseed would significantly contribute to human nutrition and health, particularly in developing countries, and help meet the requirements of the predicted 50 percent increase in the world population in the next 50 years.”
“Rathore’s study”, states the article, “represents the first substantiated case where gossypol was reduced via genetic engineering that targets the genes that make the toxin.”
I bring into recollection the statement made by the Rockefeller Foundation in its 1986 annual report, which reads:
“Before widespread use can be recommended, further investigation is needed to see if lowering the dosage can eliminate undesirable side-effects without reducing its effectiveness as a contraceptive.”
In the 1997 Foundational report, Rathore is mentioned (page 68). A postdoctoral fellowship-grant was given to a certain E. Chandrakanth “for advanced study in plant molecular biology under the direction of Keerti S. Rathore, Laboratory for Crop Transformation, Texas A&M University, College Station, Texas.”
Compromising connections, in other words, for someone who claimed academic objectivity in regards to gossypol and its sterilizing effects. Rathore explained the workings of RNAi in a 2006 issue of the Proceedings of the National Academy of Sciences.
“Cottonseed toxicity due to gossypol is a long-standing problem”, Rathore said, “and people have tried to fix it but haven’t been able to through traditional plant breeding. My area of research is plant transgenics, so I thought about using some molecular approaches to address this problem.”
Rathore also mentioned the desired main funder of his work without actually saying the name:
“we are trying to find some partners and will probably be looking at charitable foundations to help us out in terms of doing all kinds of testing that is required before a genetically engineered plant is approved for food or feed. We are in the very early stages and have a lot of ideas in mind, but we need to pursue those. Hopefully, we can find some sort of partnership that will allow us to do them.”
He also expressed the final adaptation of the cottonseed for widespread use is something of the long term:
“(…) right now there are many hurdles when you are dealing with a genetically modified plant. But I think in the next 15 or 20 years a lot of these regulations that we have to satisfy will be eliminated or reduced substantially.”
The Foundation, as is evident from the statements of Rockefeller’s own Deborah Delmer, is more than interested. Even worse, through the process of readying gossypol for mass-distribution in food, the fulfillment of their longstanding goal of sterilizing the masses into oblivion comes closer into view.
In its 1968 yearly report, the Rockefeller Foundation acknowledged funding the development of so-called “anti-fertility vaccines” and their implementation on a mass-scale. From page 51 onward we read:
“(…) several types of drugs are known to diminish male fertility, but those that have been tested have serious problems of toxicity. Very little work is in progress on immunological methods, such as vaccines, to reduce fertility, and much more research is required if a solution is to be found here.”
The possibility of using vaccines to reduce male fertility was something that needed to be investigated further, according to the Rockefeller Foundation, because both the oral pill and the IUD were not suitable for mass-scale distribution:
“We are faced with the danger that within a few years these two “modern” methods, for which such high hopes have been held, will in fact turn out to be impracticable on a mass scale.”
The possibility of administrating hormone preparations to reduce fertility was also mentioned, although- states the report- they have been known to “cause bleeding problems, which may limit their usefulness.”
“A semipermanent or renewable subcutaneous implant of these hormones has been suggested, but whether or not the same difficulties would result has not been determined.”
Saying that research thus-far had been too low-grade to produce any substantial results, the report was adamant:
“The Foundation will endeavour to assist in filling this important gap in several ways:
1- “Seeking out or encouraging the development of, and providing partial support to, a few centres of excellence in universities and research institutions in the United States and abroad in which the methods and points of view of molecular biology are teamed with the more traditional approaches of histology, embryology,and endocrinology in research pertinent to development of fertility control methods;”
2- “Supporting research of individual investigators, oriented toward development of contraceptive methods or of basic information on human reproduction relevant to such developments;”
3- “Encouraging, by making research funds available, as well as by other means, established and beginning investigators to turn their attention to aspects of research in reproductive biology that have implications for human fertility and its control;”
4- “Encouraging more biology and biochemistry students to elect careers in reproductive biology and human fertility control, through support of research and teaching programs in departments of zoology, biology, and biochemistry.”
The list goes on and on. Motivation for these activities, according to the RF?
“There are an estimated five million women among America’s poverty and near-poverty groups who need birth control service (…). The unchecked fertility of the indigent does much to perpetuate poverty, undereducation, and underemployment, not only in urban slums, but also in depressed rural areas.”
It wasn’t long before all the Foundation’s efforts began to have effect. In its annual report of 1988, The RF was happy to report the progress made by the Foundation’s Population Division in the field of anti-fertility vaccines:
“India’s National Institute of Immunology successfully completed in 1988 the first phase of trials with three versions of an anti-fertility vaccine for women. Sponsored by the government of India and supported by the Foundation, the trials established that with each of the tested vaccines, at least one year of protection against pregnancy could be expected, based on the levels of antibodies formed in response to the immunization schedule.”
In its 1997 review of anti-fertility vaccines, Indian based International Centre for Genetic Engineering and Biotechnology didn’t forget to acknowledge its main benefactor:
“The work on LHRH and HCG vaccines was supported by research grants of The Rockefeller Foundation, (…).”
In the 1990s the work on anti-fertility vaccines went in overdrive, especially in third-world nations, as did the funding provided by the deep pockets of the Rockefeller Foundation. At the same time, the target-population of the globalists- women- began to stir uncomfortably with all this out-in-the-open talk of population reduction and vaccines as a means to achieve it.
Betsy Hartman, Director of the Population and Development Program at Hampshire College, Massachusetts and “someone who believes strongly in women’s right to safe, voluntary birth control and abortion”, is no supporter of the anti-fertility vaccine, as brought into being by the Rockefeller Foundation. She explains in her essay Population control in the new world order:
“Although one vaccine has been tested on only 180 women in India, it is being billed there as ‘safe, devoid of any side effects and completely reversible’. The scientific community knows very well that such assertions are false – for instance, many questions still remain about the vaccine’s long-term impact on the immune system and menstrual cycle. There is also evidence on film of women being denied information about the vaccine in clinical trials. Nevertheless, the vaccine is being prepared for large-scale use.”
The Women’s Global Network for Reproductive Rights based in Amsterdam, the Netherlands, quoted “a leading contraceptive researcher as saying:
“Immunological birth control methods will be an ‘antigenic weapon’ against the reproductive process, which left unchecked, threatens to swamp the world.”
Animal rights activist ms. Sonya Ghosh also expressed concerns about the Rockefeller-funded anti-fertility vaccine and its implementation:
“Instead of giving individual women more options to prevent pregnancy and protect against AIDs and sexually transmitted diseases, the anti fertility vaccine is designed to be easily administered to large numbers of women using the least resources. If administered to illiterate populations the issues of user control and informed consent are further cause for concern.”
To avoid such debates, the Foundation has in the last couple of decades consorted to its long-practised and highly successful methods of either outright lying through its teeth or using deceptive language to hide the fact that it continues to work tirelessly toward its long-stated mission. If you think the RF and others have abandoned their anti-fertility efforts with the help of vaccines, think again or read this article.
Part 2: Global Distribution of Rockefeller-Funded Anti-Fertility Vaccine Coordinated by WHO
In addition to the recent PrisonPlanet-exclusive Rockefeller Foundation Developed Vaccines For “Mass-Scale” Fertility Reduction- which outlines the Rockefeller Foundation’s efforts in the 1960s funding research into so-called “anti-fertility vaccines”- another series of documents has surfaced, proving beyond any doubt that the UN Population Fund, World Bank and World Health Organization picked up on it, further developing it under responsibility of a “Task Force on Vaccines for Fertility Regulation”.
Just four years after the Rockefeller Foundation launched massive funding-operations into anti-fertility vaccines, the Task Force was created under auspices of the World Health Organization, World Bank and UN Population Fund. Its mission, according to one of its members, to support:
“basic and clinical research on the development of birth control vaccines directed against the gametes or the preimplantation embryo. These studies have involved the use of advanced procedures in peptide chemistry, hybridoma technology and molecular genetics as well as the evaluation of a number of novel approaches in general vaccinology. As a result of this international, collaborative effort, a prototype anti-HCG vaccine is now undergoing clinical testing, raising the prospect that a totally new family planning method may be available before the end of the current decade.”
In regards to the scope of the Task Force’s jurisdiction, the Biotechnology and Development Monitor reported:
“The Task Force acts as a global coordinating body for anti-fertility vaccine R&D in the various working groups and supports research on different approaches, such as anti-sperm and anti-ovum vaccines and vaccines designed to neutralize the biological functions of hCG. The Task Force has succeeded in developing a prototype of an anti-hCG-vaccine.”
One of the Task Force members, P.D. Griffin, outlined the purpose and trajectory of these Fertility Regulating Vaccines. Griffin:
“The Task Force has continued to coordinate its research activities with other vaccine development programmes within WHO and with other international and national programmes engaged in the development of fertility regulating vaccines.”
Griffin also admitted to the fact that one of the purposes of the vaccines is the implementation in developing countries. Griffin:
“If vaccines could be developed which could safely and effectively inhibit fertility, without producing unacceptable side effects, they would be an attractive addition to the present armamentarium of fertility regulating methods and would be likely to have a significant impact on family planning programmes.”
Also, one of the advantages of the FRVs over “currently available methods of fertility regulation” the Task Force states, is the following (179):
“low manufacturing cost and ease of delivery within existing health services.”
Already in 1978, the WHO’s Task Force (then called Task Force on Immunological Methods for Fertility Regulation) underlined the usefulness of these vaccines in regards to the possibility of “large scale synthesis and manufacture” of the vaccine:
“The potential advantages of an immunological approach to fertility regulation can be summarized as follows: (a) the possibility of infrequent administration, possibly by paramedical personnel; (b) the use of antigens or antigen fragments, which are not pharmacologically active; and (c) in the case of antigens of known chemical structure, there is the possibility of large-scale synthesis and manufacture of vaccine at relatively low cost.”
In 1976, the WHO Expanded Programme of Research, Development and Research Training in Human Reproduction published a report, stating:
“In 1972 the Organization (…) expanded its programme of research in human reproduction to provide an international focus for an intensified effort to improve existing methods of fertility regulation, to develop new methods and to assist national authorities in devising the best ways of providing them on a continuing basis. The programme is closely integrated with other WHO research on the delivery of family planning care by health services, which in turn feeds into WHO’s technical assistance programme to governments at the service level.”
Although the term “Anti-Fertility Vaccine”, coined by the Rockefeller Foundation, was replaced by the more bureaucratic sounding “Fertility Regulating Vaccine (FRV), the programme was obviously the same. Besides, the time-line shows conclusively that the WHO, UN Population Fund and World Bank continued on a path outlined by the Rockefellers in the late 1960s. By extension, it proves that all these organization are perfectly interlocked, best captured under the header “Scientific Dictatorship”. The relationship between the WHO and the Rockefeller Foundation is intense. In the 1986 bulletin of the World Health Organization, this relationship is being described in some detail. While researching the effectiveness of “gossypol” as an “antifertility agent”, the bulletin states:
“The Rockefeller Foundation has supported limited clinical trials in China and smallscale clinical studies in Brazil and Austria. The dose administered in the current Chinese trial has been reduced from 20 mg to 10-15 mg/day during the loading phase in order to see if severe oligospermia rather than consistent azoospermia would be adequate for an acceptable, non-toxic and reversible effect. Meanwhile, both the WHO human reproduction programme and the Rockefeller Foundation are supporting animal studies to better define the mechanism of action of gossypol.”
In August of 1992, a series of meetings was held in Geneva, Switzerland, regarding “fertility regulating vaccines”. According to the document Fertility Regulating Vaccines (classified by the WHO with a limited distribution) present at those meetings were scientists and clinicians from all over the globe, including then biomedical researcher of the American Agency for International development, and current research-chief of USAID, Mr. Jeff Spieler.
In 1986 Mr. Spieler declared:
“A new approach to fertility regulation is the development of vaccines directed against human substances required for reproduction. Potential candidates for immunological interference include reproductive hormones, ovum and sperm antigens, and antigens derived from embryonic or fetal tissue.(…). An antifertility vaccine must be capable of safely and effectively inhibiting a human substance, which would need somehow to be rendered antigenic. A fertility-regulating vaccine, moreover, would have to produce and sustain effective immunity in at least 95% of the vaccinated population, a level of protection rarely achieved even with the most successful viral and bacterial vaccines. But while these challenges looked insuperable just a few years ago, recent advances in biotechnology- particularly in the fields of molecular biology, genetic engineering and monoclonal antibody production- are bringing antifertility vaccines into the realm of the feasible.”
“Vaccines interfering with sperm function and fertilization could be available for human testing by the early 1990s”, Spieler wrote.
In order for widespread use of these vaccines, Spieler writes, the vaccine must conquer “variations in individual responses to immunization with fertility-regulating vaccines”.
“Research”, he goes on to say,”is also needed in the field of “basic vaccinology”, to find the best carrier proteins, adjuvants, vehicles and delivery systems.”
In the 1992 document, the problem of “variations in individual responses” is also discussed:
“Because of the genetic diversity of human populations”, states the document, “immune responses to vaccines often show marked differences from one individual to another in terms of magnitude and duration. These differences may be partly or even completely overcome with appropriately engineered FRVs (Fertility Regulating Vaccines) and by improvements in our understanding of what is required to develop and control the immune response elicited by different vaccines.”
The picture emerging from these facts is clear. The WHO, as a global coordinating body, has since the early 70s continued the development of the Rockefeller-funded “anti-fertility vaccine”. What also is becoming clear, is that extensive research has been done to the delivery systems in which these anti-fertility components can be buried, such as regular anti-viral vaccines. It’s a mass-scale anti-fertilization programme with the aim of reducing the world’s population: a dream long cherished by the global elite.
The 1985 Rockefeller Foundation’s annual report underlined its ongoing dedication towards finding good use for the anti-fertility substance “gossypol”, or C30H30O8 – as the description reads.
“Another long-term interest of the Foundation has been gossypol, a compound that has been shown to have an antifertility effect in men, By the end of 1985, the Foundation had made grants totaling approximately $1.6 million in an effort to support and stimulate scientific investigations on the safety and efficacy of gossypol.”
In the 1986 Rockefeller Foundation annual report, the organization admits funding research into the use of fertility-reducing compounds in relation to food for “widespread use”:
“Male contraceptive studies are focused on gossypol, a natural substance extracted from the cotton plant, and identified by Chinese researchers as having an anti-fertility effect on men. Before widespread use can be recommended, further investigation is needed to see if lowering the dosage can eliminate undesirable side-effects without reducing its effectiveness as a contraceptive. The Foundation supported research on gossypol’s safety, reversibility and efficacy in seven different 1986 grants.”
In the RF’s 1988 annual report, gossypol as a contraceptive was also elaborated upon (page 22):
“Gossypol, a natural substance found in the cotton plant, continues to show promise as an oral contraceptive for men. Because it suppresses sperm production without affecting sex hormone levels, it is unique among the experimental approaches to fertility control in men. Foundation-funded scientists worldwide have assembled an aray of information about how gossypol works, and studies continue on a wide variety of its clinical applications. Dose reduction is being investigated to reduce health risks associated with the use of gossypol.”
The following year, according to the annual report, funds were allocated to several research institutions to see how this “dose reduction” could best be accomplished without interfering with the ant-fertility effects of gossypol.
The last mention of gossypol in the Foundation’s annals we find in the 1994 annual report, where funds were appropriated to the University of Innsbruck of Austria “for a study at the Institute of Physiology on the molecular action of gossypol at the cellular level.”
In 2006, NatureNews reported that RNA interference (or RNAi) was the way to go. On the one hand it would “cut the gossypol content in cottonseeds by 98%, while leaving the chemical defenses of the rest of the plant intact.” Furthermore, the article quoted Dr. Deborah P. Delmer, the Rockefeller Foundation’s associate director of food security, who was quick to bury any concern:
“Deborah Delmer, associate director of the Rockefeller Foundation in New York City and an expert in agricultural food safety, points out that a benefit of using RNAi technology is that it turns off a gene process rather than switching on a novel function. “So instead of introducing a new foreign protein, you’re just shutting down one process,” Delmer says. “In that sense, I think that the safety concerns should be far less than other GM technologies.”
A 2006, National Geographic article Toxin-Free Cottonseed Engineered; Could Feed Millions Study Says, quotes the director of the Laboratory for Crop Transformation (Texas A&M Universtity), Keerti Singh Rathore as saying:
“A gossypol-free cottonseed would significantly contribute to human nutrition and health, particularly in developing countries, and help meet the requirements of the predicted 50 percent increase in the world population in the next 50 years.”
“Rathore’s study”, states the article, “represents the first substantiated case where gossypol was reduced via genetic engineering that targets the genes that make the toxin.”
I bring into recollection the statement made by the Rockefeller Foundation in its 1986 annual report, which reads:
“Before widespread use can be recommended, further investigation is needed to see if lowering the dosage can eliminate undesirable side-effects without reducing its effectiveness as a contraceptive.”
In the 1997 Foundational report, Rathore is mentioned (page 68). A postdoctoral fellowship-grant was given to a certain E. Chandrakanth “for advanced study in plant molecular biology under the direction of Keerti S. Rathore, Laboratory for Crop Transformation, Texas A&M University, College Station, Texas.”
Compromising connections, in other words, for someone who claimed academic objectivity in regards to gossypol and its sterilizing effects. Rathore explained the workings of RNAi in a 2006 issue of the Proceedings of the National Academy of Sciences.
“Cottonseed toxicity due to gossypol is a long-standing problem”, Rathore said, “and people have tried to fix it but haven’t been able to through traditional plant breeding. My area of research is plant transgenics, so I thought about using some molecular approaches to address this problem.”
In its 1968 yearly report, the Rockefeller Foundation acknowledged funding the development of so-called “anti-fertility vaccines” and their implementation on a mass-scale. From page 51 onward we read:
“(…) several types of drugs are known to diminish male fertility, but those that have been tested have serious problems of toxicity. Very little work is in progress on immunological methods, such as vaccines, to reduce fertility, and much more research is required if a solution is to be found here.”
The possibility of using vaccines to reduce male fertility was something that needed to be investigated further, according to the Rockefeller Foundation, because both the oral pill and the IUD were not suitable for mass-scale distribution:
“We are faced with the danger that within a few years these two “modern” methods, for which such high hopes have been held, will in fact turn out to be impracticable on a mass scale.”
The possibility of administrating hormone preparations to reduce fertility was also mentioned, although- states the report- they have been known to “cause bleeding problems, which may limit their usefulness.”
“A semipermanent or renewable subcutaneous implant of these hormones has been suggested, but whether or not the same difficulties would result has not been determined.”
Saying that research thus-far had been too low-grade to produce any substantial results, the report was adamant:
“The Foundation will endeavour to assist in filling this important gap in several ways:
1- “Seeking out or encouraging the development of, and providing partial support to, a few centres of excellence in universities and research institutions in the United States and abroad in which the methods and points of view of molecular biology are teamed with the more traditional approaches of histology, embryology,and endocrinology in research pertinent to development of fertility control methods;”
2- “Supporting research of individual investigators, oriented toward development of contraceptive methods or of basic information on human reproduction relevant to such developments;”
3- “Encouraging, by making research funds available, as well as by other means, established and beginning investigators to turn their attention to aspects of research in reproductive biology that have implications for human fertility and its control;”
4- “Encouraging more biology and biochemistry students to elect careers in reproductive biology and human fertility control, through support of research and teaching programs in departments of zoology, biology, and biochemistry.”
The list goes on and on. Motivation for these activities, according to the RF?
“There are an estimated five million women among America’s poverty and near-poverty groups who need birth control service (…). The unchecked fertility of the indigent does much to perpetuate poverty, undereducation, and underemployment, not only in urban slums, but also in depressed rural areas.”
It wasn’t long before all the Foundation’s efforts began to have effect. In its annual report of 1988, The RF was happy to report the progress made by the Foundation’s Population Division in the field of anti-fertility vaccines:
“India’s National Institute of Immunology successfully completed in 1988 the first phase of trials with three versions of an anti-fertility vaccine for women. Sponsored by the government of India and supported by the Foundation, the trials established that with each of the tested vaccines, at least one year of protection against pregnancy could be expected, based on the levels of antibodies formed in response to the immunization schedule.”
In its 1997 review of anti-fertility vaccines, Indian based International Centre for Genetic Engineering and Biotechnology didn’t forget to acknowledge its main benefactor:
“The work on LHRH and HCG vaccines was supported by research grants of The Rockefeller Foundation, (…).”
In the 1990s the work on anti-fertility vaccines went in overdrive, especially in third-world nations, as did the funding provided by the deep pockets of the Rockefeller Foundation. At the same time, the target-population of the globalists- women- began to stir uncomfortably with all this out-in-the-open talk of population reduction and vaccines as a means to achieve it.
Betsy Hartman, Director of the Population and Development Program at Hampshire College, Massachusetts and “someone who believes strongly in women’s right to safe, voluntary birth control and abortion”, is no supporter of the anti-fertility vaccine, as brought into being by the Rockefeller Foundation. She explains in her essay Population control in the new world order:
“Although one vaccine has been tested on only 180 women in India, it is being billed there as ‘safe, devoid of any side effects and completely reversible’. The scientific community knows very well that such assertions are false – for instance, many questions still remain about the vaccine’s long-term impact on the immune system and menstrual cycle. There is also evidence on film of women being denied information about the vaccine in clinical trials. Nevertheless, the vaccine is being prepared for large-scale use.”
The Women’s Global Network for Reproductive Rights based in Amsterdam, the Netherlands, quoted “a leading contraceptive researcher as saying:
“Immunological birth control methods will be an ‘antigenic weapon’ against the reproductive process, which left unchecked, threatens to swamp the world.”
Animal rights activist ms. Sonya Ghosh also expressed concerns about the Rockefeller-funded anti-fertility vaccine and its implementation:
“Instead of giving individual women more options to prevent pregnancy and protect against AIDs and sexually transmitted diseases, the anti fertility vaccine is designed to be easily administered to large numbers of women using the least resources. If administered to illiterate populations the issues of user control and informed consent are further cause for concern.”
To avoid such debates, the Foundation has in the last couple of decades consorted to its long-practised and highly successful methods of either outright lying through its teeth or using deceptive language to hide the fact that it continues to work tirelessly toward its long-stated mission. If you think the RF and others have abandoned their anti-fertility efforts with the help of vaccines, think again or read this article.
Part 2: Global Distribution of Rockefeller-Funded Anti-Fertility Vaccine Coordinated by WHO
In addition to the recent PrisonPlanet-exclusive Rockefeller Foundation Developed Vaccines For “Mass-Scale” Fertility Reduction- which outlines the Rockefeller Foundation’s effortsin the 1960s funding research into so-called “anti-fertility vaccines”- another series of documents has surfaced, proving beyond any doubt that the UN Population Fund, World Bank and World Health Organization picked up on it, further developing it under responsibility of a “Task Force on Vaccines for Fertility Regulation”.
Just four years after the Rockefeller Foundation launched massive funding-operations into anti-fertility vaccines, the Task Force was created under auspices of the World Health Organization, World Bank and UN Population Fund. Its mission, according to one of its members, to support:
“basic and clinical research on the development of birth control vaccines directed against the gametes or the preimplantation embryo. These studies have involved the use of advanced procedures in peptide chemistry, hybridoma technology and molecular genetics as well as the evaluation of a number of novel approaches in general vaccinology. As a result of this international, collaborative effort, a prototype anti-HCG vaccine is now undergoing clinical testing, raising the prospect that a totally new family planning method may be available before the end of the current decade.”
In regards to the scope of the Task Force’s jurisdiction, the Biotechnology and Development Monitor reported:
“The Task Force acts as a global coordinating body for anti-fertility vaccine R&D in the various working groups and supports research on different approaches, such as anti-sperm and anti-ovum vaccines and vaccines designed to neutralize the biological functions of hCG. The Task Force has succeeded in developing a prototype of an anti-hCG-vaccine.”
One of the Task Force members, P.D. Griffin, outlined the purpose and trajectory of these Fertility Regulating Vaccines. Griffin:
“The Task Force has continued to coordinate its research activities with other vaccine development programmes within WHO and with other international and national programmes engaged in the development of fertility regulating vaccines.”
Griffin also admitted to the fact that one of the purposes of the vaccines is the implementation in developing countries. Griffin:
“If vaccines could be developed which could safely and effectively inhibit fertility, without producing unacceptable side effects, they would be an attractive addition to the present armamentarium of fertility regulating methods and would be likely to have a significant impact on family planning programmes.”
Also, one of the advantages of the FRVs over “currently available methods of fertility regulation” the Task Force states, is the following (179):
“low manufacturing cost and ease of delivery within existing health services.”
Already in 1978, the WHO’s Task Force (then called Task Force on Immunological Methods for Fertility Regulation) underlined the usefulness of these vaccines in regards to the possibility of “large scale synthesis and manufacture” of the vaccine:
“The potential advantages of an immunological approach to fertility regulation can be summarized as follows: (a) the possibility of infrequent administration, possibly by paramedical personnel; (b) the use of antigens or antigen fragments, which are not pharmacologically active; and (c) in the case of antigens of known chemical structure, there is the possibility of large-scale synthesis and manufacture of vaccine at relatively low cost.”
In 1976, the WHO Expanded Programme of Research, Development and Research Training in Human Reproduction published a report, stating:
“In 1972 the Organization (…) expanded its programme of research in human reproduction to provide an international focus for an intensified effort to improve existing methods of fertility regulation, to develop new methods and to assist national authorities in devising the best ways of providing them on a continuing basis. The programme is closely integrated with other WHO research on the delivery of family planning care by health services, which in turn feeds into WHO’s technical assistance programme to governments at the service level.”
Although the term “Anti-Fertility Vaccine”, coined by the Rockefeller Foundation, was replaced by the more bureaucratic sounding “Fertility Regulating Vaccine (FRV), the programme was obviously the same. Besides, the time-line shows conclusively that the WHO, UN Population Fund and World Bank continued on a path outlined by the Rockefellers in the late 1960s. By extension, it proves that all these organization are perfectly interlocked, best captured under the header “Scientific Dictatorship”. The relationship between the WHO and the Rockefeller Foundation is intense. In the 1986 bulletin of the World Health Organization, this relationship is being described in some detail. While researching the effectiveness of “gossypol” as an “antifertility agent”, the bulletin states:
“The Rockefeller Foundation has supported limited clinical trials in China and smallscale clinical studies in Brazil and Austria. The dose administered in the current Chinese trial has been reduced from 20 mg to 10-15 mg/day during the loading phase in order to see if severe oligospermia rather than consistent azoospermia would be adequate for an acceptable, non-toxic and reversible effect. Meanwhile, both the WHO human reproduction programme and the Rockefeller Foundation are supporting animal studies to better define the mechanism of action of gossypol.”
In August of 1992, a series of meetings was held in Geneva, Switzerland, regarding “fertility regulating vaccines”. According to the document Fertility Regulating Vaccines (classified by the WHO with a limited distribution) present at those meetings were scientists and clinicians from all over the globe, including then biomedical researcher of the American Agency for International development, and current research-chief of USAID, Mr. Jeff Spieler.
In 1986 Mr. Spieler declared:
“A new approach to fertility regulation is the development of vaccines directed against human substances required for reproduction. Potential candidates for immunological interference include reproductive hormones, ovum and sperm antigens, and antigens derived from embryonic or fetal tissue.(…). An antifertility vaccine must be capable of safely and effectively inhibiting a human substance, which would need somehow to be rendered antigenic. A fertility-regulating vaccine, moreover, would have to produce and sustain effective immunity in at least 95% of the vaccinated population, a level of protection rarely achieved even with the most successful viral and bacterial vaccines. But while these challenges looked insuperable just a few years ago, recent advances in biotechnology- particularly in the fields of molecular biology, genetic engineering and monoclonal antibody production- are bringing antifertility vaccines into the realm of the feasible.”
“Vaccines interfering with sperm function and fertilization could be available for human testing by the early 1990s”, Spieler wrote.
In order for widespread use of these vaccines, Spieler writes, the vaccine must conquer “variations in individual responses to immunization with fertility-regulating vaccines”.
“Research”, he goes on to say,”is also needed in the field of “basic vaccinology”, to find the best carrier proteins, adjuvants, vehicles and delivery systems.”
In the 1992 document, the problem of “variations in individual responses” is also discussed:
“Because of the genetic diversity of human populations”, states the document, “immune responses to vaccines often show marked differences from one individual to another in terms of magnitude and duration. These differences may be partly or even completely overcome with appropriately engineered FRVs (Fertility Regulating Vaccines) and by improvements in our understanding of what is required to develop and control the immune response elicited by different vaccines.”
The picture emerging from these facts is clear. The WHO, as a global coordinating body, has since the early 70s continued the development of the Rockefeller-funded “anti-fertility vaccine”. What also is becoming clear, is that extensive research has been done to the delivery systems in which these anti-fertility components can be buried, such as regular anti-viral vaccines. It’s a mass-scale anti-fertilization programme with the aim of reducing the world’s population: a dream long cherished by the global elite.
Part 3: On Top of Vaccines, Rockefeller Foundation Presents Anti-Fertility Substance Gossypol for “Widespread Use”
The 1985 Rockefeller Foundation’s annual reportunderlined its ongoing dedication towards finding good use for the anti-fertility substance “gossypol”, or C30H30O8 – as the description reads.
Indeed, gossypol, a toxic polyphenol derived from the cotton plant, was identified early on in the Foundation’s research as an effective sterilant. The question was, how to implement or integrate the toxic substance into crops.
“Another long-term interest of the Foundation has been gossypol, a compound that has been shown to have an antifertility effect in men, By the end of 1985, the Foundation had made grants totaling approximately $1.6 million in an effort to support and stimulate scientific investigations on the safety and efficacy of gossypol.”
In the 1986 Rockefeller Foundation annual report, the organization admits funding research into the use of fertility-reducing compounds in relation to food for “widespread use”:
“Male contraceptive studies are focused on gossypol, a natural substance extracted from the cotton plant, and identified by Chinese researchers as having an anti-fertility effect on men. Before widespread use can be recommended, further investigation is needed to see if lowering the dosage can eliminate undesirable side-effects without reducing its effectiveness as a contraceptive. The Foundation supported research on gossypol’s safety, reversibility and efficacy in seven different 1986 grants.”
In the RF’s 1988 annual report, gossypol as a contraceptive was also elaborated upon (page 22):
“Gossypol, a natural substance found in the cotton plant, continues to show promise as an oral contraceptive for men. Because it suppresses sperm production without affecting sex hormone levels, it is unique among the experimental approaches to fertility control in men. Foundation-funded scientists worldwide have assembled an aray of information about how gossypol works, and studies continue on a wide variety of its clinical applications. Dose reduction is being investigated to reduce health risks associated with the use of gossypol.”
The following year, according to the annual report, funds were allocated to several research institutions to see how this “dose reduction” could best be accomplished without interfering with the ant-fertility effects of gossypol.
(1988- $ 400,000, in addition to remaining funds from prior year appropriations) To support research on gossypol, its safety, reversibility, and efficacy as a contraceptive for use by men (…).”
Mention is made on money allocated to the University of Texas, “for a study of gossypol’s effects on DNA replication (…).”
The last mention of gossypol in the Foundation’s annals we find in the 1994 annual report, where funds were appropriated to the University of Innsbruck of Austria “for a study at the Institute of Physiology on the molecular action of gossypol at the cellular level.”
It seems that the funded scientists have indeed found a way of “lowering the dosage” of gossypol, circumventing the toxicity of the substance, so as to suppress or even eliminate these “undesirable side-effects”, which include: low blood potassium levels, fatigue, muscle weakness and even paralysis. If these effects could be eliminated without reducing the anti-fertility effects, the Foundation figured, it would be a highly effective and almost undetectable sterilant.
Although overtly, research into and development of gossypol as a anti-fertility compound was abandoned in the late 1990s, the cottonseed containing the substance was especially selected for mass distribution in the beginning of the current decade. Around 2006 a media-campaign was launched, saying the cottonseed could help defeat hunger and poverty.
In 2006, NatureNews reported that RNA interference (or RNAi) was the way to go. On the one hand it would “cut the gossypol content in cottonseeds by 98%, while leaving the chemical defenses of the rest of the plant intact.” Furthermore, the article quoted Dr. Deborah P. Delmer, the Rockefeller Foundation’s associate director of food security, who was quick to bury any concern:
“Deborah Delmer, associate director of the Rockefeller Foundation in New York City and an expert in agricultural food safety, points out that a benefit of using RNAi technology is that it turns off a gene process rather than switching on a novel function. “So instead of introducing a new foreign protein, you’re just shutting down one process,” Delmer says. “In that sense, I think that the safety concerns should be far less than other GM technologies.”
A 2006, National Geographic article Toxin-Free Cottonseed Engineered; Could Feed Millions Study Says, quotes the director of the Laboratory for Crop Transformation (Texas A&M Universtity), Keerti Singh Rathore as saying:
“A gossypol-free cottonseed would significantly contribute to human nutrition and health, particularly in developing countries, and help meet the requirements of the predicted 50 percent increase in the world population in the next 50 years.”
“Rathore’s study”, states the article, “represents the first substantiated case where gossypol was reduced via genetic engineering that targets the genes that make the toxin.”
I bring into recollection the statement made by the Rockefeller Foundation in its 1986 annual report, which reads:
“Before widespread use can be recommended, further investigation is needed to see if lowering the dosage can eliminate undesirable side-effects without reducing its effectiveness as a contraceptive.”
In the 1997 Foundational report, Rathore is mentioned (page 68). A postdoctoral fellowship-grant was given to a certain E. Chandrakanth “for advanced study in plant molecular biology under the direction of Keerti S. Rathore, Laboratory for Crop Transformation, Texas A&M University, College Station, Texas.”
Compromising connections, in other words, for someone who claimed academic objectivity in regards to gossypol and its sterilizing effects. Rathore explained the workings of RNAi in a 2006 issue of the Proceedings of the National Academy of Sciences.
“Cottonseed toxicity due to gossypol is a long-standing problem”, Rathore said, “and people have tried to fix it but haven’t been able to through traditional plant breeding. My area of research is plant transgenics, so I thought about using some molecular approaches to address this problem.”
Rathore also mentioned the desired main funder of his work without actually saying the name:
“we are trying to find some partners and will probably be looking at charitable foundations to help us out in terms of doing all kinds of testing that is required before a genetically engineered plant is approved for food or feed. We are in the very early stages and have a lot of ideas in mind, but we need to pursue those. Hopefully, we can find some sort of partnership that will allow us to do them.”
He also expressed the final adaptation of the cottonseed for widespread use is something of the long term:
“(…) right now there are many hurdles when you are dealing with a genetically modified plant. But I think in the next 15 or 20 years a lot of these regulations that we have to satisfy will be eliminated or reduced substantially.”
The Foundation, as is evident from the statements of Rockefeller’s own Deborah Delmer, is more than interested. Even worse, through the process of readying gossypol for mass-distribution in food, the fulfillment of their longstanding goal of sterilizing the masses into oblivion comes closer into view.
In its 1968 yearly report, the Rockefeller Foundation acknowledged funding the development of so-called “anti-fertility vaccines” and their implementation on a mass-scale. From page 51 onward we read:
“(…) several types of drugs are known to diminish male fertility, but those that have been tested have serious problems of toxicity. Very little work is in progress on immunological methods, such as vaccines, to reduce fertility, and much more research is required if a solution is to be found here.”
The possibility of using vaccines to reduce male fertility was something that needed to be investigated further, according to the Rockefeller Foundation, because both the oral pill and the IUD were not suitable for mass-scale distribution:
“We are faced with the danger that within a few years these two “modern” methods, for which such high hopes have been held, will in fact turn out to be impracticable on a mass scale.”
The possibility of administrating hormone preparations to reduce fertility was also mentioned, although- states the report- they have been known to “cause bleeding problems, which may limit their usefulness.”
“A semipermanent or renewable subcutaneous implant of these hormones has been suggested, but whether or not the same difficulties would result has not been determined.”
Saying that research thus-far had been too low-grade to produce any substantial results, the report was adamant:
“The Foundation will endeavour to assist in filling this important gap in several ways:
1- “Seeking out or encouraging the development of, and providing partial support to, a few centres of excellence in universities and research institutions in the United States and abroad in which the methods and points of view of molecular biology are teamed with the more traditional approaches of histology, embryology,and endocrinology in research pertinent to development of fertility control methods;”
2- “Supporting research of individual investigators, oriented toward development of contraceptive methods or of basic information on human reproduction relevant to such developments;”
3- “Encouraging, by making research funds available, as well as by other means, established and beginning investigators to turn their attention to aspects of research in reproductive biology that have implications for human fertility and its control;”
4- “Encouraging more biology and biochemistry students to elect careers in reproductive biology and human fertility control, through support of research and teaching programs in departments of zoology, biology, and biochemistry.”
The list goes on and on. Motivation for these activities, according to the RF?
“There are an estimated five million women among America’s poverty and near-poverty groups who need birth control service (…). The unchecked fertility of the indigent does much to perpetuate poverty, undereducation, and underemployment, not only in urban slums, but also in depressed rural areas.”
It wasn’t long before all the Foundation’s efforts began to have effect. In its annual report of 1988, The RF was happy to report the progress made by the Foundation’s Population Division in the field of anti-fertility vaccines:
“India’s National Institute of Immunology successfully completed in 1988 the first phase of trials with three versions of an anti-fertility vaccine for women. Sponsored by the government of India and supported by the Foundation, the trials established that with each of the tested vaccines, at least one year of protection against pregnancy could be expected, based on the levels of antibodies formed in response to the immunization schedule.”
In its 1997 review of anti-fertility vaccines, Indian based International Centre for Genetic Engineering and Biotechnology didn’t forget to acknowledge its main benefactor:
“The work on LHRH and HCG vaccines was supported by research grants of The Rockefeller Foundation, (…).”
In the 1990s the work on anti-fertility vaccines went in overdrive, especially in third-world nations, as did the funding provided by the deep pockets of the Rockefeller Foundation. At the same time, the target-population of the globalists- women- began to stir uncomfortably with all this out-in-the-open talk of population reduction and vaccines as a means to achieve it.
Betsy Hartman, Director of the Population and Development Program at Hampshire College, Massachusetts and “someone who believes strongly in women’s right to safe, voluntary birth control and abortion”, is no supporter of the anti-fertility vaccine, as brought into being by the Rockefeller Foundation. She explains in her essay Population control in the new world order:
“Although one vaccine has been tested on only 180 women in India, it is being billed there as ‘safe, devoid of any side effects and completely reversible’. The scientific community knows very well that such assertions are false – for instance, many questions still remain about the vaccine’s long-term impact on the immune system and menstrual cycle. There is also evidence on film of women being denied information about the vaccine in clinical trials. Nevertheless, the vaccine is being prepared for large-scale use.”
The Women’s Global Network for Reproductive Rights based in Amsterdam, the Netherlands, quoted “a leading contraceptive researcher as saying:
“Immunological birth control methods will be an ‘antigenic weapon’ against the reproductive process, which left unchecked, threatens to swamp the world.”
Animal rights activist ms. Sonya Ghosh also expressed concerns about the Rockefeller-funded anti-fertility vaccine and its implementation:
“Instead of giving individual women more options to prevent pregnancy and protect against AIDs and sexually transmitted diseases, the anti fertility vaccine is designed to be easily administered to large numbers of women using the least resources. If administered to illiterate populations the issues of user control and informed consent are further cause for concern.”
To avoid such debates, the Foundation has in the last couple of decades consorted to its long-practised and highly successful methods of either outright lying through its teeth or using deceptive language to hide the fact that it continues to work tirelessly toward its long-stated mission. If you think the RF and others have abandoned their anti-fertility efforts with the help of vaccines, think again or read this article.
Part 2: Global Distribution of Rockefeller-Funded Anti-Fertility Vaccine Coordinated by WHO
In addition to the recent PrisonPlanet-exclusive Rockefeller Foundation Developed Vaccines For “Mass-Scale” Fertility Reduction- which outlines the Rockefeller Foundation’s efforts in the 1960s funding research into so-called “anti-fertility vaccines”- another series of documents has surfaced, proving beyond any doubt that the UN Population Fund, World Bank and World Health Organization picked up on it, further developing it under responsibility of a “Task Force on Vaccines for Fertility Regulation”.
Just four years after the Rockefeller Foundation launched massive funding-operations into anti-fertility vaccines, the Task Force was created under auspices of the World Health Organization, World Bank and UN Population Fund. Its mission, according to one of its members, to support:
“basic and clinical research on the development of birth control vaccines directed against the gametes or the preimplantation embryo. These studies have involved the use of advanced procedures in peptide chemistry, hybridoma technology and molecular genetics as well as the evaluation of a number of novel approaches in general vaccinology. As a result of this international, collaborative effort, a prototype anti-HCG vaccine is now undergoing clinical testing, raising the prospect that a totally new family planning method may be available before the end of the current decade.”
In regards to the scope of the Task Force’s jurisdiction, the Biotechnology and Development Monitor reported:
“The Task Force acts as a global coordinating body for anti-fertility vaccine R&D in the various working groups and supports research on different approaches, such as anti-sperm and anti-ovum vaccines and vaccines designed to neutralize the biological functions of hCG. The Task Force has succeeded in developing a prototype of an anti-hCG-vaccine.”
One of the Task Force members, P.D. Griffin, outlined the purpose and trajectory of these Fertility Regulating Vaccines. Griffin:
“The Task Force has continued to coordinate its research activities with other vaccine development programmes within WHO and with other international and national programmes engaged in the development of fertility regulating vaccines.”
Griffin also admitted to the fact that one of the purposes of the vaccines is the implementation in developing countries. Griffin:
“If vaccines could be developed which could safely and effectively inhibit fertility, without producing unacceptable side effects, they would be an attractive addition to the present armamentarium of fertility regulating methods and would be likely to have a significant impact on family planning programmes.”
Also, one of the advantages of the FRVs over “currently available methods of fertility regulation” the Task Force states, is the following (179):
“low manufacturing cost and ease of delivery within existing health services.”
Already in 1978, the WHO’s Task Force (then called Task Force on Immunological Methods for Fertility Regulation) underlined the usefulness of these vaccines in regards to the possibility of “large scale synthesis and manufacture” of the vaccine:
“The potential advantages of an immunological approach to fertility regulation can be summarized as follows: (a) the possibility of infrequent administration, possibly by paramedical personnel; (b) the use of antigens or antigen fragments, which are not pharmacologically active; and (c) in the case of antigens of known chemical structure, there is the possibility of large-scale synthesis and manufacture of vaccine at relatively low cost.”
In 1976, the WHO Expanded Programme of Research, Development and Research Training in Human Reproduction published a report, stating:
“In 1972 the Organization (…) expanded its programme of research in human reproduction to provide an international focus for an intensified effort to improve existing methods of fertility regulation, to develop new methods and to assist national authorities in devising the best ways of providing them on a continuing basis. The programme is closely integrated with other WHO research on the delivery of family planning care by health services, which in turn feeds into WHO’s technical assistance programme to governments at the service level.”
Although the term “Anti-Fertility Vaccine”, coined by the Rockefeller Foundation, was replaced by the more bureaucratic sounding “Fertility Regulating Vaccine (FRV), the programme was obviously the same. Besides, the time-line shows conclusively that the WHO, UN Population Fund and World Bank continued on a path outlined by the Rockefellers in the late 1960s. By extension, it proves that all these organization are perfectly interlocked, best captured under the header “Scientific Dictatorship”. The relationship between the WHO and the Rockefeller Foundation is intense. In the 1986 bulletin of the World Health Organization, this relationship is being described in some detail. While researching the effectiveness of “gossypol” as an “antifertility agent”, the bulletin states:
“The Rockefeller Foundation has supported limited clinical trials in China and smallscale clinical studies in Brazil and Austria. The dose administered in the current Chinese trial has been reduced from 20 mg to 10-15 mg/day during the loading phase in order to see if severe oligospermia rather than consistent azoospermia would be adequate for an acceptable, non-toxic and reversible effect. Meanwhile, both the WHO human reproduction programme and the Rockefeller Foundation are supporting animal studies to better define the mechanism of action of gossypol.”
In August of 1992, a series of meetings was held in Geneva, Switzerland, regarding “fertility regulating vaccines”. According to the document Fertility Regulating Vaccines (classified by the WHO with a limited distribution) present at those meetings were scientists and clinicians from all over the globe, including then biomedical researcher of the American Agency for International development, and current research-chief of USAID, Mr. Jeff Spieler.
In 1986 Mr. Spieler declared:
“A new approach to fertility regulation is the development of vaccines directed against human substances required for reproduction. Potential candidates for immunological interference include reproductive hormones, ovum and sperm antigens, and antigens derived from embryonic or fetal tissue.(…). An antifertility vaccine must be capable of safely and effectively inhibiting a human substance, which would need somehow to be rendered antigenic. A fertility-regulating vaccine, moreover, would have to produce and sustain effective immunity in at least 95% of the vaccinated population, a level of protection rarely achieved even with the most successful viral and bacterial vaccines. But while these challenges looked insuperable just a few years ago, recent advances in biotechnology- particularly in the fields of molecular biology, genetic engineering and monoclonal antibody production- are bringing antifertility vaccines into the realm of the feasible.”
“Vaccines interfering with sperm function and fertilization could be available for human testing by the early 1990s”, Spieler wrote.
In order for widespread use of these vaccines, Spieler writes, the vaccine must conquer “variations in individual responses to immunization with fertility-regulating vaccines”.
“Research”, he goes on to say,”is also needed in the field of “basic vaccinology”, to find the best carrier proteins, adjuvants, vehicles and delivery systems.”
In the 1992 document, the problem of “variations in individual responses” is also discussed:
“Because of the genetic diversity of human populations”, states the document, “immune responses to vaccines often show marked differences from one individual to another in terms of magnitude and duration. These differences may be partly or even completely overcome with appropriately engineered FRVs (Fertility Regulating Vaccines) and by improvements in our understanding of what is required to develop and control the immune response elicited by different vaccines.”
The picture emerging from these facts is clear. The WHO, as a global coordinating body, has since the early 70s continued the development of the Rockefeller-funded “anti-fertility vaccine”. What also is becoming clear, is that extensive research has been done to the delivery systems in which these anti-fertility components can be buried, such as regular anti-viral vaccines. It’s a mass-scale anti-fertilization programme with the aim of reducing the world’s population: a dream long cherished by the global elite.
Part 3: On Top of Vaccines, Rockefeller Foundation Presents Anti-Fertility Substance Gossypol for “Widespread Use”
It seems there is no limit to the Rockefeller Foundation’s ambitions to introduce anti-fertility compounds into either existing “health-services”, such as vaccines, or- as appears to be the case now- average consumer-products.
Indeed, gossypol, a toxic polyphenol derived from the cotton plant, was identified early on in the Foundation’s research as an effective sterilant. The question was, how to implement or integrate the toxic substance into crops.
In the 1986 Rockefeller Foundation annual report, the organization admits funding research into the use of fertility-reducing compounds in relation to food for “widespread use”:
“Male contraceptive studies are focused on gossypol, a natural substance extracted from the cotton plant, and identified by Chinese researchers as having an anti-fertility effect on men. Before widespread use can be recommended, further investigation is needed to see if lowering the dosage can eliminate undesirable side-effects without reducing its effectiveness as a contraceptive. The Foundation supported research on gossypol’s safety, reversibility and efficacy in seven different 1986 grants.”
In the RF’s 1988 annual report, gossypol as a contraceptive was also elaborated upon (page 22):
“Gossypol, a natural substance found in the cotton plant, continues to show promise as an oral contraceptive for men. Because it suppresses sperm production without affecting sex hormone levels, it is unique among the experimental approaches to fertility control in men. Foundation-funded scientists worldwide have assembled an aray of information about how gossypol works, and studies continue on a wide variety of its clinical applications. Dose reduction is being investigated to reduce health risks associated with the use of gossypol.”
The following year, according to the annual report, funds were allocated to several research institutions to see how this “dose reduction” could best be accomplished without interfering with the ant-fertility effects of gossypol.
(1988- $ 400,000, in addition to remaining funds from prior year appropriations) To support research on gossypol, its safety, reversibility, and efficacy as a contraceptive for use by men (…).”
Mention is made on money allocated to the University of Texas, “for a study of gossypol’s effects on DNA replication (…).”
It seems that the funded scientists have indeed found a way of “lowering the dosage” of gossypol, circumventing the toxicity of the substance, so as to suppress or even eliminate these “undesirable side-effects”, which include: low blood potassium levels, fatigue, muscle weakness and even paralysis. If these effects could be eliminated without reducing the anti-fertility effects, the Foundation figured, it would be a highly effective and almost undetectable sterilant.
Although overtly, research into and development of gossypol as a anti-fertility compound was abandoned in the late 1990s, the cottonseed containing the substance was especially selected for mass distribution in the beginning of the current decade. Around 2006 a media-campaign was launched, saying the cottonseed could help defeat hunger and poverty.
“Deborah Delmer, associate director of the Rockefeller Foundation in New York City and an expert in agricultural food safety, points out that a benefit of using RNAi technology is that it turns off a gene process rather than switching on a novel function. “So instead of introducing a new foreign protein, you’re just shutting down one process,” Delmer says. “In that sense, I think that the safety concerns should be far less than other GM technologies.”
A 2006, National Geographic article Toxin-Free Cottonseed Engineered; Could Feed Millions Study Says, quotes the director of the Laboratory for Crop Transformation (Texas A&M Universtity), Keerti Singh Rathore as saying:
“A gossypol-free cottonseed would significantly contribute to human nutrition and health, particularly in developing countries, and help meet the requirements of the predicted 50 percent increase in the world population in the next 50 years.”
“Rathore’s study”, states the article, “represents the first substantiated case where gossypol was reduced via genetic engineering that targets the genes that make the toxin.”
I bring into recollection the statement made by the Rockefeller Foundation in its 1986 annual report, which reads:
“Before widespread use can be recommended, further investigation is needed to see if lowering the dosage can eliminate undesirable side-effects without reducing its effectiveness as a contraceptive.”
In the 1997 Foundational report, Rathore is mentioned (page 68). A postdoctoral fellowship-grant was given to a certain E. Chandrakanth “for advanced study in plant molecular biology under the direction of Keerti S. Rathore, Laboratory for Crop Transformation, Texas A&M University, College Station, Texas.”
Compromising connections, in other words, for someone who claimed academic objectivity in regards to gossypol and its sterilizing effects. Rathore explained the workings of RNAi in a 2006 issue of the Proceedings of the National Academy of Sciences.
“Cottonseed toxicity due to gossypol is a long-standing problem”, Rathore said, “and people have tried to fix it but haven’t been able to through traditional plant breeding. My area of research is plant transgenics, so I thought about using some molecular approaches to address this problem.”
Rathore also mentioned the desired main funder of his work without actually saying the name:
“we are trying to find some partners and will probably be looking at charitable foundations to help us out in terms of doing all kinds of testing that is required before a genetically engineered plant is approved for food or feed. We are in the very early stages and have a lot of ideas in mind, but we need to pursue those. Hopefully, we can find some sort of partnership that will allow us to do them.”He also expressed the final adaptation of the cottonseed for widespread use is something of the long term:
“(…) right now there are many hurdles when you are dealing with a genetically modified plant. But I think in the next 15 or 20 years a lot of these regulations that we have to satisfy will be eliminated or reduced substantially.”The Foundation, as is evident from the statements of Rockefeller’s own Deborah Delmer, is more than interested. Even worse, through the process of readying gossypol for mass-distribution in food, the fulfillment of their longstanding goal of sterilizing the masses into oblivion comes closer into view.
Full Article
Full Article
Wednesday, September 29, 2010
"Vaccinations in GMO Corn For Pigs"
AMES, IOWA — Iowa State University researchers are putting flu vaccines into the genetic makeup of corn, which may someday allow pigs and humans to get a flu vaccination simply by eating corn or corn products.
“We’re trying to figure out which genes from the swine influenza virus to incorporate into corn so those genes, when expressed, would produce protein,” said Hank Harris, professor in animal science and one of the researchers on the project. “When the pig consumes that corn, it would serve as a vaccine.”
This collaborative effort project involves Mr. Harris and Brad Bosworth, an affiliate associate professor of animal science working with pigs, and Kan Wang, a professor in agronomy, who is developing the vaccine traits in the corn.According to the researchers, the corn vaccine would also work in humans when they eat corn or even corn flakes, corn chips, tortillas or anything that contains corn, Mr. Harris said. The research is funded by a grant from Iowa State University’s Plant Sciences Institute, and is their Biopharmaceuticals and Bioindustrials Research Initiative.
If the research goes well, the corn vaccine may be possible in five to seven years. In the meantime, the team is trying to expedite the process. “While we’re waiting for Wang to produce the corn, we are starting initial experiments in mice to show that the vaccine might induce an immune response,” Mr. Bosworth said.
Mr. Harris said the team still needs more answers. “The big question is whether or not these genes will work when given orally through corn,” he added. “That is the thing we’ve still got to determine.”
Stability and safety are several advantages to the corn vaccine. Once the corn with the vaccine is grown, it can be stored for long-term without losing its potency, researchers claim. If a swine flu virus breaks out, the corn could be shipped to the location to try to vaccinate animals and humans in the area quickly. Because corn grain is used as food and feed, there is no need for extensive vaccine purification, which can be an expensive process.
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