Genetic Terraforming
is the
NEW Eugenics!
The idea of genetic terraforming is nothing new. Even though the name has changed over millennia, the idea
remains the same. To create a perfect and healthy human being that lives forever without God, being god in itself.
The ideas I present in this power point presentation are also nothing new to those who study diligently, but I would
like to offer some alternative thoughts to some of these subjects that have been repeatedly parroted across the
“truthers” scene. Since no one can know for sure what the future will bring. What we are given, the Holy Bible, we
must disseminate the contents with what is available to us in technology and information. We can base a lot of the
Bibles teaching and compare them to what we see happening in the world around us, but the greater picture and
the final fulfillment of such prophecies cannot be fully realized unless we are watching as Christ commanded all
His disciples to do in the end of this age. By watching, we can realize the clearer picture of the Word of God.
We are a privileged people to serve the Lord in the end of this age as we are privy to what the prophet Daniel
wanted to know about all these things hundreds of years ago. Daniel was told to “go his way” (Dan. 12:9) because
the end of the age was not a concern for him as told by the Lord. It should be apparent to all of us why God told
Daniel to not concern himself with such things. Even from twenty years ago our world has become so radically
different. It would have been unbeneficial to Daniel to know of these things to live his life out in his own
generation. Technology is superseding itself almost on a daily basis. Colonizing other planets are no longer the
things of science fiction but science fact.
At the Tower of Babel, the Lord dispersed the people from being united by causing them all to speak a different language. The idea most scholars
share as to why the Lord did this was to fulfill the command in Genesis 1:28 to “replenish the Earth.” It is a part of Yahweh’s plan to cause the
whole Earth to be inhabited so that by the end of the 6,000 year plan of God for mankind that the gospel and His work would go throughout the
entire planet and not just one particular place. The Tower of Babel was an affront to God on many levels. Namely, uniting the people under the
mighty hand of Nimrod and not of Yahweh. Nimrod tried to do that which was not his to do, to become the second Adam. This was the Son of God’s
desire and Yahweh’s plan to divest Himself of His station and to become a man, fully man, fully God, and to die for mankind's sins so that the chance
would be given that man may come back to his Creator and live in unity with Him.
At the Tower of Babel, in mankind's mind, the idea was placed that he could imagine himself to be his own creator, independent from the source
from whence he was made. With the absence of “God” from his life, mankind was free from the restraints of moral obligations that would have
directed his footsteps in the ways of righteousness. Instead, mankind let his imagination roam free, where ever it inspired feelings of grandeur,
mans feet moved quickly to follow after its illusions.
Our world today reflects this very same construction that caused the Flood, the rebellion of Nimrod, and the rise and fall of every civilization of man.
Each time this tide of imagination comes back into mankind's thoughts a little more is learned from past mistakes. Corrections are made and a better
course laid out. Each time the struggle resumes only to end in collapse and utter failure.
We are again witnessing another swell coming upon the Earth. This time it is a culmination of all the knowledge learned over the past 6,000 years
of mankind's time on the Earth. Christ was not merely making a statement but was prophesying when He said, “for then there will be great
oppression, such as has not been from the beginning of the world until now, no, nor ever will be (Matthew 24:21 WEB, see also Dan. 12:1; Ezek. 5:9;
Job 2:2; Rev. 16:18; etc…).” Each time the tide has come in the greater the abomination against God and thus the greater the judgments sent by God
on an unrepenting mankind.
Mankind is climbing up the Tower again, but this time it is not simply a building made by man as Babel was created, but it is now the very
foundation of creation itself. The battle for the reigns of creation is escalating towards its climax here in the end of days. The presentation herein,
contains just a fraction of all the pieces of the puzzle many have been trying to fit together for millennium. The prize sought after by the unruly
imagination is to become god. Since the Garden of Eden, man has ever desired to be like God and partook of the Tree of the Knowledge of Good and
Evil. Mankind, in its shortsightedness, never even realized that Yahweh had all ready had this in His mind. To make a family of God out of
mankind.
Many are called, but few are chosen.
Only those who chose to follow Christ and learn from Him of righteousness will enter the Kingdom of Heaven.
Those who reject the Son of God and continue in their own imaginations will perish.
The rise of humanity as both a hybrid and as a genetically engineered species is as real
today in the 21st Century as it was back in Noah’s day. Beside the fact that Jesus
warned us, “Mat 24:37-But as the days of Noe were, so shall also the coming of the
Son of man be,” we must begin to realize that there is NOTHING NEW under the Sun
and that we are making the gravest mistakes all over again as the human species.
Genetic Terra-forming is also nothing new. Satan introduced this concept to the
human race back in Genesis 6. Further details of this “intrusion” into human genome
by fallen angels can be found in extra Biblical works such as the Book of Jasher, the
Book of Enoch (Ethiopian translation is most accurate), and the Book of the Wars of
the Lord (Num. 21:14), etc…. Satan’s goal has always been to get as many human
being to rebel against Yahweh in heaven and to cause as many to be deceived that they
can be children of God (Yahweh).
The LIE of “evolution” has now officially become the LIE of “Panspermia”.
[1] http://www.telegraph.co.uk/news/newstopics/howaboutthat/11256420/DNA-can-survive-re-entry-intoEarths-atmosphere.html
http://www.logosapologia.org/stage-is-set-for-panspermia-creation-myth/
http://www.buzzle.com/articles/is-there-life-on-other-planets.html
If not Panspermia, then it could be artificial life created in a lab.
On the surface all these ideas look great, appealing to our deepest human dreams to not be “ill” any more in this
world and to have a healthy and abundant life, but what awaits the darker side of this tale. Could/would there ever
be a reason to not want to be immortal in this body?
http://www.theguardian.com/science/2013/oct/13/craig-ventner-mars
Human Longevity, Inc
On March 4, 2014 Venter and co-founders Peter Diamandis and Robert Hariri announced the formation of Human Longevity,
Inc, a company focused on extending the healthy, "high performance", human lifespan.[46][47][48] At the time of the announcement
the company had already raised $70 million in venture financing, which was expected to last 18 months.[46][47] Venter is the
chairman and chief executive officer (CEO). The company said that it plans to sequence 40,000 genomes per year, with an initial
focus on cancer genomes and the genomes of cancer patients.[46]
Human Longevity's mission is to extend healthy human lifespan by the use of high-resolution big data diagnostics from genomics,
metabolomics, microbiomics, and proteomics, and the use of stem cell therapy.[49] http://en.wikipedia.org/wiki/Craig_Venter
However the feat of resurrecting the dead or creating new life, the goal is all one in the same.
Create man to live forever as his own god.
This pace of advancing technology is not only staggering to the mind, but extremely out of touch with over 80% of
humanity.
The themes of genetic classism and discrimination and of elitist
scientists “playing God” resonate widely in our culture (from
Shelley’s Frankenstein to GATTACA to the X-Men). Indeed, the
extensive coverage of a study on the genetics of IQ that is
currently underway at the Beijing Genomics Institute (BGI)
suggests that the media knows a good story when it sees it. It
seems to me that this has attracted attention not because of any
scientific advance or discovery (the study has not yet been
completed) but because of the way those involved and
commenting on it have acted as cheerleaders for the idea of
prenatal prediction and selection.
Here’s Prof. Geoffrey Miller (of NYU), in an interview for an
article egregiously entitled “China is engineering genius babies”
on vice.com (whatever that is):
“How does Western research in genetics compare to China’s?
We’re pretty far behind. We have the same technical
capabilities, the same statistical capabilities to analyze the data,
but they’re collecting the data on a much larger scale and seem
to be capable of transforming the scientific findings into
government policy and consumer genetic testing much more
easily than we are. Technically and scientifically we could be
http://www.wiringthebrain.com/2013/05/the-new-eugenics-same-as-olddoing this, but we’re not.”
eugenics.html?showComment=1368455558914#c5821418481283745282
A growing number commentators from within the scientific community are arguing for a revisitation of eugenics:
“Seeing the bright side of being handicapped is like praising the virtues of extreme poverty. To be sure, there are
many individuals who rise out of its inherently degrading states. But we perhaps most realistically should see it as
the major origin of asocial behavior that has among its bad consequences the breeding of criminal violence.”
(James Watson, “Genes and Politics,” 1997)
“We are once again practicing a sort of eugenics” (Matt Ridley, “The New Eugenics,” 2000)
In 2001, the conservative theorist Richard Lynn published Eugenics: A Reassessment, which argues just what you
think it does. In 2002, researcher DJ Galton (no relation to the founder of eugenics) considered the new genetics,
test-tube babies, and genetic screening and called a spade a spade: Eugenics: The Future of Human Life in the 21st
Century.
“Eugenics failed because it was not scientific enough…The role of eugenics in our time is in maximizing
[hereditary] information and its availability to those who need it and minimizing the temptation to use the State as
the means of enforcing eugenic ideals.” (Elof Carlson, “The Eugenic World of Charles Benedict Davenport,” 2008)
“A new interest in rational discourse about eugenics…should be our goal.” (Maynard Olson, “Davenport’s Dream,”
2008)
“Soon it will be a sin of parents to have a child that carries the heavy burden of genetic disease. We are entering a
world where we have to consider the quality of our children.” (Bob Edwards [creator of first test-tube baby])
“Eugenics, once discredited as part of the first wave of social authoritarian progressives that trampled free will for
women, handicapped people and minorities, is attempting a 21st century comeback.” (Hank Campbell, “Genetic
Literacy Project on Neo-Eugenics,” 2012)
“To a great extent we already live in the second age of eugenics.” (Razib Khan, “Eugenics, the 100 year cycle”, 2012)
http://genotopia.scienceblog.com/337/is-eugenics-ever-okay/
The most recent is Jon Entine, who runs the Center for Genetic Literacy and writes regularly for the conservative
money magazine Forbes. “Instead of being driven by a desire to ‘improve’ the species,” he writes, the “new eugenics
is driven by our personal desire to be as healthy, intelligent and fit as possible—and for the opportunity of our
children to be so as well.” (Jon Entine, “DNA Screening is Part of the New Eugenics—and That’s Okay,” 2013)
http://genotopia.scienceblog.com/337/is-eugenics-ever-okay/
The biomedical industry hides truly fantastic profits behind the cloak of “health.” Moving responsibly into this
inevitable future demands that someone call out the self-interest of the diagnostics and pharmaceutical companies,
the instrument-makers and laboratories, the hospitals, the advertisers, and the investors in this new age gold mine.
It demands analysis of subtle forms of coercion. It demands a jaundiced eye. Skepticism isn’t Luddism, isn’t antichoice, isn’t anti-health. It’s following the money.
Much as one might wish to do so, the genie can’t be stuffed back into the bottle. The new eugenics is here. This
worries me greatly. But worry, by itself, solves nothing. The concerns it raises are too complex for either dogmatism
or complacency. It comes with new, subtle kinds of coercion. Science alone cannot be our guide into this brave
genetic world. The closer we come to guiding our own evolution, the more important a humanistic perspective—
one that takes the long view of history and the broad view of social context—becomes in helping us make sense of
it. The future is here, and, dammit, it’s complicated. http://genotopia.scienceblog.com/337/is-eugenics-ever-okay/
When will mankind finally understand that for all its good intentions, or greatest desires for longevity that we are
not the author of life and death. A greater being, Yahweh, has all ready told us the beginning from the ending and
now mankind must live out this prophecy as foretold by God. Many are called, but few are saved.
Compatibility of genes with all the human race.
Once the rapture of the bride takes place (Rev. 12:5), the bema judgment seat of Christ will take place. The left
behind Laodicean church will go into the wilderness for 1260 days (Rev. 12:6) – They will have a small amount of
time to prepare before Satan is cast to the Earth. Then war will break out in heaven. Archangel Michael and his
angels will fight against Satan and his angels (Rev. 12:7). Satan will be kicked out of heaven along with his angels
(Rev. 12:8-10) and will turn on the Laodicean church and persecute her greatly (Rev. 12:11-17).
When Satan and his angels fall to the Earth, they will use this crisis to their advantage and show themselves as
“aliens” and make “first contact” with the Earth. The Vatican has been preparing for this for years and now openly
says they will baptize these creatures into the Church.
In the near future, I believe it will coincide with the mass exodus of Israeli’s into Israel, a global genetic screening
will begin.
This global screening will help the “aliens” or fallen angels to start a massive vaccination or similar injection
method, on a global scale to change mankind from being a sick and dying human being into a immortal half breed
(Nephilim) hybrid. This will be the Mark of the Beast. If you take the Mark, you will forever separated from
Yahweh in heaven, forever.
I say all this now after studying scripture for years, that what we are seeing with Ebola is the very beginning of this
insidious mast plan to destroy the human race by taking potential human children of God and corrupting them
into the family of Satan.
Global Genetic Testing Market to Reach US$2.2 Billion by 2017, According to New Report by Global Industry
Analysts, Inc.
GIA announces the release of a comprehensive global report on the Genetic Testing market. The global market for Genetic Testing
is forecast to reach US$2.2 billion by 2017. Increasing knowledge about the potential benefits in genetic testing is one of the
prime reasons for the growth of the genetic testing market. Advancements in the genetic testing space, aging population and a
subsequent rise in the number of chronic diseases, and increasing incidence of cancer cases are the other factors propelling
growth in the genetic testing market.
Genetic testing represents the most rapidly expanding segment of the molecular diagnostics market worldwide. Growing incidence
of genetic diseases unravels new opportunities for genetic testing. The transformation of genetic testing from being a servicedriven market to a product-driven market is expected to provide an impetus to the diagnostic companies for the expansion of
their operations. The market for screening the newborns, diagnosing rare and fatal disorders, and predicting the probability of
occurrence of diseases is likely to expand. Particularly, genetic tests to screen the newborns are expected to expand immensely
over the coming years.
As each individual’s genetic structure differs, there is a need to develop a method that can be customized as per the individual
needs. One of the major issues faced by the industry is the urgent need to employ standard regulations with regard to procedures
employed during the genetic testing process. Lack of credible standard procedure has led to the fear among individuals regarding
the authenticity of genetic reports. Genetic counseling services are on the rise, specifically in the US. Presently, there are around
2,780 certified genetic counselors operating in the United States.
Major players profiled in the report include Abbott Laboratories, Abbott Molecular Inc., Applied Biosystems Inc., AutoGenomics
Inc., BioRad Laboratories, Celera Group, ELITech Group, PerkinElmer Inc., Quest Diagnostics Inc., Roche Diagnostics Corp., Roche
Molecular Diagnostics Inc., Transgenomic Inc., among others.
Folks, this is their words. BTW - Chemtrails may only be an end to a means by
corrupting DNA on a global scale to introduce their “saving serum”.
http://www.biomedtrends.com/GetDetails.asp?CatName=Genetic%20Testing
National Geographic is at the head of this global genetic
mandate!
Gathering the Mayo Genes
The Genographic Project is a multi-year global research initiative using DNA to map the history of
human migration. Dr. Spencer Wells, National Geographic Explorer-in-Residence and a population
geneticist, said his team are looking forward to unveiling Mayo’s genetic history. “This provides a great
citizen science opportunity — and the more people who participate, the more our scientific knowledge
will grow. We are excited to have the opportunity to return to Mayo to share the results of the Geno 2.0
Study.”
This novel project is another initiative from the Enterprise and Investment Unit at Mayo County Council
and a flagship event for 2013, the year of the Gathering. Head of the Enterprise and Investment Unit
Joanne Grehan welcomed the National Geographic team back to Mayo, saying “We are delighted that
our friends from National Geographic are returning to reveal the results of the Mayo Genographic
Study. This has been a superb opportunity for the people of Mayo to play their part in uncovering the
mysteries of our ancestors. We hope the findings from this research will assist in mapping the genetic
journey of both our County and Humankind.” http://www.mayo.ie/dnn/NewsSports/GenographicProject.aspx#.VGSob7ZhGSo
https://genographic.nationalgeographic.com/
Why is IBM teaming up with National Geographic?
Is IBM up to their old tricks again?
In the early 1880s, Herman Hollerith (1860–1929), a young employee at the U.S. Census Bureau, conceived of the idea of
creating readable cards with standardized perforations, each representing specific individual traits such as gender, nationality,
and occupation. The millions of punched cards created for the population counted in the national census could then be sorted on
the basis of specific bits of information they contained—thereby providing a quantified portrait of the nation.[2] In 1910, the
German licensee Willy Heidinger established the Deutsche Hollerith Maschinen Gesellschaft (German Hollerith Machine
Corporation), known by the acronym "Dehomag."[3] The next year, Hollerith sold his American business to industrialist Charles
Flint (1850–1934) for $1.41 million ($34 million in 2012 dollars).[4] The counting machine operation was made part of a new
conglomerate called the Computing-Tabulating-Recording Company (CTR).[4] Flint chose Thomas J. Watson (1874–1956), the
star salesman of the National Cash Register Corporation, to head the new operation.[5] The German licensee Dehomag later
became a direct subsidiary of the American corporation CTR.[6] In 1924, Watson assumed the role of Chief Executive Officer of
CTR and renamed the company International Business Machines (IBM).
Black details the ongoing business relationship between Watson's IBM and the emerging German regime headed by Adolf Hitler
and his National Socialist German Workers Party (NSDAP). Hitler came to power in January 1933; on March 20 of that same year
he established a concentration camp for political prisoners in the Bavarian town of Dachau, just outside the city of Munich.
Repression against political opponents and the country's substantial ethnic Jewish population began at once. By April 1933, some
60,000 had been imprisoned.[7] Business relations between IBM and the Hitler regime continued uninterrupted in the face of
broad international calls for an economic boycott.[8] Indeed, Willy Heidinger, who remained in control of Dehomag, the 90%owned German subsidiary of IBM, was an enthusiastic supporter of the Hitler regime.[9]
http://en.wikipedia.org/wiki/IBM_and_the_Holocaust
On April 12, 1933, the German government announced plans to conduct a long-delayed national census.[10] The project was particularly important
to the Nazis as a mechanism for the identification of Jews, Gypsies, and other ethnic groups deemed undesirable by the regime. Dehomag offered to
assist the German government in its task of ethnic identification, concentrating upon the 41 million residents of Prussia.[11] This activity was not only
countenanced by Thomas Watson and IBM in America, Black argues, but was actively encouraged and financially supported, with Watson himself
traveling to Germany in October 1933 and the company ramping up its investment in its German subsidiary from 400,000 to 7,000,000
Reichsmark—about $1 million.[12] This injection of American capital allowed Dehomag to purchase land in Berlin and to construct IBM's first
factory in Germany, Black charges, thereby "tooling up for what it correctly saw as a massive financial relationship with the Hitler regime."[12]
Black also asserts that a "secret deal" was made between Heidinger and Watson during the latter's visit to Germany which allowed Dehomag
commercial powers outside of Germany, enabling the "now Nazified" company to "circumvent and supplant" various national subsidiaries and
licensees by "soliciting and delivering punch card solution technology directly to IBM customers in those territories."[13] As a result, Nazi Germany
soon became the second most important customer of IBM after the lucrative US market, Black notes.[14] The 1933 census, with design help and
tabulation services provided by IBM through its German subsidiary, proved to be pivotal to the Nazis in their efforts to identify, isolate, and
ultimately destroy the country's Jewish minority. Machine-tabulated census data greatly expanded the estimated number of Jews in Germany by
identifying individuals with only one or a few Jewish ancestors. Previous estimates of 400,000 to 600,000 were abandoned for a new estimate of 2
million Jews in the nation of 65 million.[15]
As the Nazi war machine occupied successive nations of Europe, capitulation was followed by a census of the population of each subjugated nation,
with an eye to the identification and isolation of Jews and Gypsies. These census operations were intimately intertwined with technology and cards
supplied by IBM's German and new Polish subsidiaries, which were awarded specific sales territories in Poland by decision of the New York office
following Germany's successful Blitzkrieg invasion.[16] Data generated by means of counting and alphabetization equipment supplied by IBM
through its German and other national subsidiaries was instrumental in the efforts of the German government to concentrate and ultimately destroy
ethnic Jewish populations across Europe, Black demonstrates.[17] Black reports that every Nazi concentration camp maintained its own HollerithAbteilung (Hollerith Department), assigned with keeping tabs on inmates through use of IBM's punchcard technology.[18] In his book, Black charges
that "without IBM's machinery, continuing upkeep and service, as well as the supply of punch cards, whether located on-site or off-site, Hitler's
camps could have never managed the numbers they did."[19]
http://en.wikipedia.org/wiki/IBM_and_the_Holocaust
IBM - Pioneering Genetic Privacy
In October 2005, IBM became the first major corporation in the world to establish a genetics privacy policy. It
prohibits current or future employees’ genetic information from being used in employment decisions. In an allcompany announcement, CEO Sam Palmisano explained, “It has been IBM’s long-standing policy not to
discriminate against people because of their heritage or who they are. A person’s genetic makeup may be the most
fundamental expression of both.”
Spurring landmark US privacy legislation
IBM’s genetics privacy policy underscores one of
the company’s guiding principles: that individual
rights should be protected by corporate policy
even when lawmakers aren’t yet at the table.
IBM’s 2005 policy came three years in advance of
the US Genetic Information Nondiscrimination
Act (GINA), which IBM supported in
congressional testimony. The first wrongful
termination lawsuit under GINA was filed by a
Connecticut woman fired by her employer soon
after she tested positive for BRCA2, one of two
known breast cancer genes. In total, 201 GINA
charges were filed in 2010.
http://www-03.ibm.com/ibm/history/ibm100/us/en/icons/geneticprivacy/
Championing Privacy by Design
In another example of IBM’s
commitment to preserving the
individual’s right to privacy, the
company has been a leader in helping
to implement Privacy by Design—the
approach of embedding privacy tools
into technologies and systems as they
are built. For example, in a
collaborative Smart Grid project in
Ontario, Canada, IBM teamed with one
of the region’s electricity providers to
help develop an operationally
improved electrical grid that also helps
safeguard sensitive personal
information—such as work habits and
shower schedules—that data from
smart meters can reveal.
http://www-03.ibm.com/ibm/history/ibm100/us/en/icons/geneticprivacy/
Did you catch the “Single
Eye” in the picture!!!!
Breakthrough privacy research
IBM researchers are hard at work on
the next generation of privacyprotection technologies. In 2009, IBM
computer scientist Craig Gentry
unveiled his fully homomorphic
encryption breakthrough, which
enables computer systems to perform
calculations on encrypted data without
decrypting it. The technique allows
users to hand off data processing to a
third party, while simultaneously
barring access to that data. Gentry’s
resulting honors include the Privacy
Innovation Award from the
International Association of Privacy
Professionals in 2009, and the 2010
Privacy Enhancing Technology Award.
http://www-03.ibm.com/ibm/history/ibm100/us/en/icons/geneticprivacy/
The watershed policy extended four decades of IBM leadership on issues of personal privacy. IBM has been able to anticipate both
its own information needs and the impact of technology-enabled advances as they ripple out to larger society—while enabling
data flows and undertaking a conscientious public response.
Executives at IBM had been quietly considering a genetics privacy policy for several years. In 2005, a landmark research
endeavor pushed the issue front and center. IBM and the National Geographic Society embarked on a project to gather the
world’s largest collection of human genetic samples in an effort to map human migratory history, and IBMers were encouraged
to participate.
IBM Chief Privacy Officer, Vice President and Security Counsel Harriet Pearson remembers the response vividly. “A lot of
questions and concerns from employees began appearing in my inbox, along the lines of, ‘You’re asking us to take a cheek
swab—what are you going to do with the DNA?’” she recalls. “That really prompted a conversation as we began to consider the
societal-level implications of the project.”
Research on developments outside of IBM showed that employee desire for reassurance was well founded. While national
legislation and government-provided healthcare shielded many workers in developed economies throughout Europe and Asia
from genetic discrimination, disturbing stories had begun to emerge in the US and Australia. Individuals there were reportedly
being treated differently after they were found to be carriers of genetic markers that indicated heightened risk for costly diseases.
Such discrimination clearly harmed individuals—but it also had broader societal implications. If genetic data and medical
histories could not be shared safely, many of the life-saving advances being pursued in medicine—and the promise held out by
genetic testing and other innovations in the emerging field of personalized medicine—might be thwarted.
To IBM, this wasn’t simply a practical problem to be managed. It was a matter of values and policy. The company pledged that
employees’ genetic data—if such data were ever to be shared with the company—would be handled with a high degree of
security and respect for privacy, and would not factor into hiring decisions or eligibility for foundational health insurance. The
global policy, a first among corporations, also predated US federal legislation protecting all Americans from genetic
discrimination in the workplace, which wouldn’t arrive for another three years. In 2007, Pearson, the architect of IBM’s policy,
testified before the US Congress, helping to push the Genetic Information Nondiscrimination Act, or GINA, into law on May 21,
2008.
11 companies that helped the Nazi
Buy the Kit – oh yeah, membership is FREE!
http://www.yourgeneticgenealogist.com/2012/10/geno-20-its-in-mail.html
http://shop.nationalgeographic.com/ngs/browse/productDetail.jsp?productId=2001246&gsk&code=MR20936
http://shop.nationalgeographic.com/ngs/browse/productDetail.jsp?productId=2001246&gsk&code=MR20936
About the test
National Geographic Explorer-in-Residence Dr. Spencer Wells and team designed Geno 2.0 based on the new technologies and insights that
emerged since the launch of the Genographic Project in 2005. Using an exclusive, custom-built genotyping chip, we test nearly 150,000 DNA
markers that have been specifically selected to provide unprecedented ancestry-related information.
By participating, you will:
• Discover the migration paths your ancient ancestors followed hundreds—even thousands—of years ago, with an unprecedented view of your
ancestral journey.
• Learn what percentage of your genome is affiliated with specific regions of the world.
• Find out if you have Neanderthal or Denisovan ancestry. (Or if you are a Nephilim)
• Have the opportunity to share your story and connect with other Genographic Project participants, helping us fill in the gaps in the human story.
What's included in the Geno 2.0 DNA Test kit:
The Geno 2.0 kit contains everything you need to begin the journey into your past, including painless cheek swabs and instructions for submitting
your DNA samples (return postage required). Plus, we’ve designed the Geno 2.0 kit box to serve as a beautiful keepsake to store your results after
you access them online.
How your participation helps the Genographic Project:
The Genographic Project is an ambitious attempt to help answer fundamental questions about where humankind originated and how we came to
populate the Earth. Using the latest genetic and computational technologies to analyze historical patterns in DNA from participants around the
world, our team of world-renowned scientists led by Dr. Spencer Wells, seeks to reveal our migratory history and to better understand the
connections and differences that make up humankind.
As a Genographic Project participant, you will have the opportunity to contribute your data to our Genographic database, helping our
scientists and researchers who are working to chart a comprehensive map of the early stages of human history. Participation in the Genographic
Project database is your choice and is not necessary to access your individual results.
And a portion of the proceeds from the sales of Geno 2.0 kits are channeled back into the project to support additional research and to fund cultural
conservation and revitalization efforts for indigenous communities around the world through the Genographic Legacy Fund.
The Genographic project is
not about finding out where human beings
came from.
THE HOLY BIBLE ALL READY TELLS US THIS IN GENESIS. We all come
from Noah’s loins through his sons Ham, Shem or Japheth.
All the people on the Earth come from these three genetic lines.
Interestingly, most people can trace their genetic lines all the way back
through their mother’s lineage, but to make it “easier” Satan and his
minions have provided a cheap test for you to take.
The Great Genetic Culling
Will your genetic lineage survive?
(NaturalNews) The "Great Culling" of the human population has quietly begun. Covertly, insidiously, mercilessly, a global
depopulation agenda has been launched. As this plays out, the vast majority of the human race will be removed from the gene
pool. Genetically annihilated. Will you and your genetic lineage survive?
First, let's dismiss any idea that the great culling is some sort of fanciful conspiracy theory. World power brokers like Bill Gates
and Ted Turner openly discuss reducing the world population by 90%. Bill Gates, in particular, happily funds infertility
technologies, vaccines and GMOs, all of which are purposely designed to cause infertility and halt new baby births, thereby
sharply contracting the human population.
The Bill and Melinda Gates Foundation, for example provided significant funding to the University of North Carolina to develop
ultrasound infertility technology that could render human sperm unviable for up to six months. Reported by the BBC, this
technology was proven effective on rats, and it's only one of 78 different research projects the Gates Foundation has funded under
the guise of "global health programs."
http://www.naturalnews.com/034834_Bill_Gates...
Bill Gates famously explained his depopulation agenda through the use of vaccines with this quote, delivered to a live TED
audience in 2010:
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.
(http://www.naturalnews.com/029911_vaccines_B...)
http://www.naturalnews.com/036756_depopulation_agenda_eugenics_survivor.html
"Eliminate the weak"
That this is the desire of the global controllers is no secret. It's not debated. This is what today's politicians,
bureaucrats and even some misinformed activists of the "environmental" movement wish to achieve -- the
reduction of world population to under one billion people. To them, humanity is seen as a threat to the planet and
even to itself.
From one point of view, this analysis may actually be correct. It's difficult to see how today's mindless masses of
dumbed-down consumers -- steeped in video games, television and junk food -- can offer any meaningful
contributions to the future of human civilization. So, from the point of view of the global controllers, "culling the
herd" of humanity is actually a good thing. It makes humanity stronger, they say, in much the same way that
culling the weaklings from a herd of wild animals improves the aggregate gene pool of the targeted species as a
whole.
The globalists argue that today's human gene pool is stalled. The weak and the stupid reproduce just as much as
everybody else -- if not more so. The human gene pool is actually devolving, they say, and the only way to bring it
back to a point where we have a species capable of reaching for the stars is to eliminate those who aren't smart
enough to deserve a spot in the human gene pool.
The word for this is, of course, eugenics. Adolf Hitler pursued the same philosophy: Improve the human race
through genocide. Eliminate the weak, the ugly, the stupid. Fire up the incinerators, disarm the target race to be
exterminated, and herd them into gas chambers or open pits.
http://www.naturalnews.com/036756_depopulation_agenda_eugenics_survivor.html
Modern eugenics
Toda's eugenicists are more subtle. They've learned, through experience, that openly gassing entire populations doesn't win over the hearts and
minds of the public. So they've developed covert methods of accomplishing the same thing. These coverts methods include convincing people to eat
genetically modified foods -- which promote infertility -- to drink fluoride, take vaccines, use synthetic chemicals, increase abortions and pursue
other actions that either kill people outright or drastically reduce rates of reproduction.
The idea behind these is that, first off, the culling of the human race can now be accomplished without all the horrifying images of Nazi Germany's
gas chambers. While the Jews in World War II had to be forcibly lined up and herded into railroad cars, today's eugenics victims willfully line up at
pharmacies to be injected with flu vaccines containing stealth cancer viruses that accomplish the same thing: Death.
Death by vaccines is just slower and more covert than death by Zyklon B.
The great intelligence test
Importantly, the genocidal properties of vaccines, GMOs, chemical food additives, medications and other synthetic chemicals function as a sort of
intelligence test for the population. Those who routinely take vaccines are, of course, stupid. Removing the stupid people -- the "useless eaters" -from the gene pool is one of the goals of the global controllers. Thus, vaccine propaganda serves as the perfect filter for removing "stupid genes"
from the human gene pool. This is no doubt why globalists so aggressively push vaccines on low-income families -- they equate "low income" with
"not qualified to reproduce."
Importantly, vaccines contain stealth cancer viruses that are passed along through multiple generations. The SV40 viruses introduced to the
population through polio vaccines in the 1950's still exists today in the grandchildren of those who were first vaccinated. This is openly admitted by
top scientists who helped develop these vaccines (http://www.naturalnews.com/033584_Dr_Maurice...).
Meanwhile, the efficacy of these vaccines is completely and utterly fabricated, as has been exposed by two whistleblower scientists who blew the lid
on scientific fraud taking place at Merck (http://www.naturalnews.com/036328_Merck_mump...).
Many pharmaceuticals directly cause infertility, by the way. Propecia, a Merck baldness drug, has now been linked to infertility and ejaculation
disorders (http://www.naturalnews.com/035568_male_baldn...).
http://www.naturalnews.com/036756_depopulation_agenda_eugenics_survivor.html
The 7 threats to your survival and fertility
1) GMOs - Engineered to grow poisonous chemicals right in the crops themselves, GMOs are also designed to cause reproductive failure in any
mammal consuming them.
2) Vaccines - Loaded with stealth cancer viruses and chemical adjuvants, vaccines are the primary cause behind today's rising rates of infertility,
birth defects and spontaneous abortions. Vaccines are aggressively pushed in minority neighborhoods and low-income areas.
3) Chemtrails - Formulated with aluminum, barium and other heavy metals, chemtrails cause human exposure to toxic metals that impair brain
function and neurological function. This exposure may contribute to birth defects and deformities, but details need to be further explored.
4) Prescription medications - Prescription drugs and chemotherapy damage DNA, promote impotence and decrease both sperm quality and egg
quality.
5) Chemical food additives - These chemicals damage DNA and egg quality, causing infertility to be passed down through multiple generations of
females. What you eat today can damage the eggs of your great-great-great granddaughter. Poisons in the food supply right now include sodium
nitrite (in nearly all processed meats), MSG, aspartame and chemical preservatives.
6) Biological weapons release - A possible "fast kill" scenario being explored by world governments, a biological weapons release can burn through
the population with high kill rates while being conveniently blamed on any desired scapegoat such as a fictional terrorist group. "We are at war
with Eurasia!"
7) Food fascism leading to starvation - Corporations like Monsanto are seeking total global domination (and corporate ownership) over the entire
food supply. This concept is called "food fascism," and it would allow corporations and governments to determine who eats and who starves. Notice
how home gardens are under attack? (http://www.naturalnews.com/032960_Julie_Bass...) Raw milk centers are raided at gunpoint?
(http://www.naturalnews.com/033220_Rawesome_F...) Backyard ranching is being criminalized?
(http://www.naturalnews.com/035585_Michigan_f...) This is all part of the food fascism assault that's already underway in our world.
Those are the top threats to your survival and fertility. What follows next is how to beat them.
http://www.naturalnews.com/036756_depopulation_agenda_eugenics_survivor.html
The 10 strategies for beating the odds and winning the survivor game
#1) Avoid all poisons - These means eliminating all GMOs, fluoride, aspartame, MSG, artificial fragrances, chemical medications, chemical food additives and all other synthetic chemicals
from your life. For most families, this means gutting your pantry, bathroom counters, garage chemicals and lawn care chemicals. Remember: The globalist controllers refuse to eat GMO and
consume only organic foods. Ever wonder why? Because they know the chemical-laden, genetically modified foods are being used to kill off the uninformed masses.
#2) Use nutrition to protect your DNA - This is absolutely crucial. Good nutrition (superfoods, high mineralization, antioxidants, plant concentrates, etc.) can prevent DNA damage from
exposure to low-levels of radiation as well as toxic chemicals. Above all, good nutrition boosts reproductive health, sperm quality, egg quality, and even brain function (so you think more
clearly and don't get suckered into globalist propaganda).
#3) Do not vaccinate your children - This is a key defense against the great culling. Those who vaccinate their children condemn them to increased risks of infertility, thereby putting their
entire genetic line at risk of annihilation. By avoiding vaccines and allowing your children to naturally experience the chicken pox or measles, you actually make them stronger and more
resistant to future infections.
#4) Grow your own food - The only food you can truly trust is food you grow yourself. Using heirloom seeds, ocean water trace mineral concentrates, soil probiotics and rainwater, grow
food that nourishes your body and brain. Save your seeds and re-plant them each season. Over time, they will adapt to your specific soils and climate, improving yields and seed viability. See
our heirloom survival seed solution at: http://www.supplysource.com/surthrival-seed-...
#5) Learn skills of self defense and physical security - Be prepared to physically defend your life, home and property against tyrants, looters, criminals or even zombies (!). Learn the
fundamental skills of self defense, weapon competency and marksmanship. I teach this information in a downloadable preparedness course at:
http://programs.webseed.com/Health_Ranger_Li...
#6) Reject mainstream propaganda - In order to protect your mind, you must refuse to subject yourself to the mind-numbing propaganda of the mainstream media. This means throwing
out your television, shutting off cable news, and shifting to information sources such as truth-telling websites and books.
#7) Do not try to "save" everyone. Most of the masses will be culled. They are already beyond hope, having been poisoned with fluoride, vaccines, GMOs and other chemicals into a state of
total denial. Have compassion for them, for they are the last of their kind. But do find other aware and informed survivors and get to know them. Share skills and knowledge. Form a
community defense plan for a worst-case scenario possibility. Cross-train each other to spread skills across the group. There is strength in numbers.
#8) Follow a philosophy of core redundancies. Examine all the critical infrastructure necessary to support your life -- food, water, heat, shelter, emergency medicine, defense,
communications, etc. -- and put at minimum a second layer of redundancy in place for each one.
#9) Train yourself for mental adaptability. In order to survive, you must not allow yourself to ever be locked into the "tunnel vision" of narrow thinking. To survive, you must be able to
adapt, solve problems, and use resources in innovative ways. Training for this can include solving mental puzzles (including playing "problem solving" puzzle video games), exploring the
outdoors, learning new skills (such as juggling), and trying out new hobbies. Do not let your mind stagnate. You will need it to be flexible.
#10) Avoid radiation exposure. Nothing damages your DNA faster than radiation, and sources of radiation are all around us. From the TSA body scanners at the airport to the CT scans
ordered by your doctor, these harmful, ionizing radiation procedures damage your DNA and compromise fertility. Avoid using cell phones, Smart Meters and even wi-fi, if possible.
Especially avoid medical imaging scans, dental X-rays and security scans of all kinds. Radiation damage is cumulative, meaning it gets progressively worse over time as you are exposed to
repeated doses of low-level radiation.
http://www.naturalnews.com/036756_depopulation_agenda_eugenics_survivor.html
DNA in the News
Sorenson Molecular Genealogy Foundation is First to Adopt Genetic Genealogy’s New Industry Standard for
Reporting Y-DNA Profiles - Earth Times - 17 Aug 2009
Man with amnesia searches for clues - The Wichita Eagle - 16 Aug 2009
Family trait: Local man’s DNA project traces Pike family histories - The Telegram - 12 Aug 2009
The Gerstenberger clan is seeking the roots of a big family tree - Los Angeles Times - 8 Aug 2009
Amelia Earhart Mystery May Soon be Solved - Blisstree.com - 6 Aug 2009
DNA Proves Scottish Roots of Haley Family - Ancestry Magazine - Jul 2009
DNA Brings Genealogies Closer Together - Ancestry Magazine - Jul 2009
Sheba, NYU researchers to draw genetic map of wandering Jew - Jerusalem Post - 20 Jul 2009
For more articles:
http://www.isogg.org/newsarchives.htm
http://www.isogg.org/newsletter/2009/aug.html
Why is Ebola such a BIG DEAL!
Scientist Working on Gov’t Ebola Drug Joked About Culling Population with GMO Virus
NOT THE GUY YOU WANT MAKING THE EBOLA VACCINE: Drugmaker said “Go out and use genetic engineering
to create a better virus… 25 percent of the population is supposed to go in Contagion.”
Media coverage is now focusing on the experimental Ebola treatments being given to two American Ebola patients
who contracted it while caring for victims in Africa — the site of the world’s deadliest outbreak.
But that Ebola treatment was developed by a leading bioengineering scientist at the Arizona State University
Biodesign Institute who was caught on camera “joking” about wiping out humanity. Dr. Charles Arntzen suggested
the use of a “better” genetically engineered virus during a post-lecture Q&A focused on over-population issues,
citing the 2011 Hollywood film ‘Contagion.’
As Truthstream Media previously reported, on February 2, 2012, Dr. Charles Arntzen, head of The Biodesign
Institute for Infectious Diseases and Vaccinology, responded to a question pertaining to whether feeding some eight
billion people in the world was worth it, or whether population reduction should be pursued.
In response, Dr. Arntzen quipped:
“Has anybody seen ‘Contagion’? That’s the answer! Go out and use genetic engineering to create a better virus…
25 percent of the population is supposed to go in Contagion.”
While this comment was made prior to the current Ebola outbreak fears, it is unsettling given the fact that Dr.
Arntzen was already working a biotech vaccine for Ebola.
http://truthstreammedia.com/scientist-working-on-govt-ebola-drug-joked-about-culling-population-with-gmo-virus/
Tom Beal of Tuscon.com wrote: Arntzen, who pioneered the process of producing antigenic proteins from
genetically modified plants, said he and his colleagues had been working on a vaccine for Ebola, using tobacco
plants. Arntzen told Beal:
“I was involved in the initial research funded by the U.S. Army, which gave a grant to ASU, and the idea was we
would use plant biotechnology to make both a vaccine and the monoclonal antibody.”
Among the many high level projects Dr. Arntzen has worked on for DARPA, as well as private biotech industry
include an edible vaccine with genetically engineered medicine/vitamins grown into foods like bananas and even
work on bioterrorism vaccine antigens for U.S. Biowarfare Defense alongside Mitch Hein, the founder of Epicyte –
the biotech firm that created spermicidal anti-bodies grown in corn to slow human reproduction.
A great deal of related research into other bioweapon treatments is directly based upon Dr. Charles Arntzen’s
pioneering research.
Among these experimental treatments are a storable genetically engineered Anthrax vaccine for use during a
biological attack, as well as research into biopharmaceutical treatments for the plague, cholera and other infectious
diseases that could create a pandemic.
In light of this background, statements like the one made by Arntzen hardly convey trust in a process that is
already less than transparent and prone to speculation, various states of unrest and panic on the part of the public.
The Daily Mail reported that much of the local population in Sierra Leone have been distrustful of medical workers
there and blamed the deaths on a ‘government conspiracy’.
Someone casually remarking on culling some 25% of the population with a bioweapon is THE LAST PERSON you’d
want to trust with creating an already dangerous countermeasure to Ebola, which carries a death rate as high as
90%.
And yet, that is exactly who has been leading this biowarfare research for decades now…
http://truthstreammedia.com/scientist-working-on-govt-ebola-drug-joked-about-culling-population-with-gmo-virus/
Sources include:
Edible Vaccine Inventor Jokes about Culling Population with GMO Virus
Ebola treatment pioneered at ASU
U.S. BIOWARFARE DEFENSE: A Cost-Effective Strategy to Create Highly Efficacious Strategic Reserves of
Therapeutics and Vaccines
Banana Vaccines: A Conversation with Dr. Charles Arntzen
Harvest of Fear: PBS Interviews Dr. Charles Arntzen
Charles Arntzen Regents’ Professor; Co-Dir., Center for Infectious Diseases & Vaccinology
Journal of Environmental Health Perspectives: PLANT vs. PATHOGEN: Enlisting Tobacco in the Fight Against
Anthrax
GM corn set to stop man spreading his seed
‘What’s shocking is how Ebola patients look before they die': British doctor working in Sierra Leone describes the
horror of deadly disease
Vaccines in Your Vegetables : Genetic gardeners are trying to grow crops that could save millions of lives. Their
discoveries might make immunizing a child against hepatitis as easy as eating a banana
http://truthstreammedia.com/scientist-working-on-govt-ebola-drug-joked-about-culling-population-with-gmo-virus/
White House admits staging fake vaccination operation to gather DNA from the public
Learn more:
http://www.naturalnews.com/045318_fake_vaccines_DNA_harvesting_White_House.html#ixzz3Ixi8VYZq
The five biggest lies about Ebola being pushed by government and mass media
Learn more:
http://www.naturalnews.com/047089_Ebola_pandemic_government_lies_disinformation.html#ixzz3IxiMMGIH
Why does the CDC own a patent on Ebola 'invention?'
Learn more: http://www.naturalnews.com/046290_Ebola_patent_vaccines_profit_motive.html#ixzz3IxiQmkXR
A One World Global
Health System is being
Formed.
The ISPOR Global Health Care Systems Road Map
To click on the area in which you live, you’ll have to visit the link below to get the clickable map.
This information was initially developed by the Global Health Care Reimbursement Systems and Decision Processes
Working Group and Health Technology Assessment (HTA) of Medical Devices & Diagnostics Working Group under
HTA SIG.
An article entitled Health Care System Information Sharing was published in Value Health Regional Issues that
references the development and quality assurance of this information. The reference citation is: Eldessouki R, Smith
MD. Health Care System Information Sharing: A Step Toward Better Health Globally. Value Health Regional Issues
2012; 1: 118-129.
http://www.ispor.org/htaroadmaps/
I brought this website to your attention not simply because of the realization that the One World Government,
Religion, Health Care, et al…, but that I found something interesting that should be pointed out in the actual map
itself. When I click on the individual countries, I notice that these two are “normal” with the exception of a few
countries in South America that are not mentioned (compare side map):
Maybe it’s just that these countries haven’t “signed on” to this Global Health Program yet and so they are not
included in the map????
I click on Africa and the only country listed there is Egypt. I still don’t see anything too unusual, but it is weird that
Lybia is not involved, nor is Ethiopia, as both of these countries are very prominently displayed in Ezekiel 38-39.
This next one I can not explain as a fluke.
http://www.ispor.org/htaroadmaps/
Ummmm….
Where’s Russia?
Not only is Russia not listed where they are geographically supposed to be, BUT the WHOLE MIDDLE EAST isn’t
even included. So did the Arabs decide that they want to be apart of Asian Health Care System? What about Israel?
They are one of the leaders in Health Technology and Services.
Oh WAIT!!!! Check the next slide.
http://www.ispor.org/htaroadmaps/
I placed a current map (as of 1999) of Russia. I do not know how they got Russia to squeeze into Europe map
system, but as you can see in the list, Russia is listed inside Europe. I began to realize after looking through a
majority of this website that this is all “plans” that will take effect in the One World Government AFTER Ezekiel
38-39 take place. Am I just speculating here???
http://www.ispor.org/htaroadmaps/
One World Government = always displayed with Single Eye
http://www.ispor.org/vision2020.asp
ISPOR may be a global entity to watch as health care across the world is becoming
standardized through “systems” that will put everyone on the same field. This
integration of our own unique traditional health care in many 3rd world countries will
become a thing of the past. You will see a corporate doctor of the corporation you
find yourself working for and just like in the past, you will work for Paternalism or the
Company Town. Many will know what I’m talking about if you know someone who
lived in West Virginia or Kentucky in the early 1900’s (there are many others) These
coal mining towns had slaves who thought they were free by getting a pay check then
spending it all at the Company Store, which was owned by the company.
http://www.ispor.org/htaroadmaps/
DARPA is now officially
involved in EVERY aspect of
world affairs.
Is the U.S. Military Manufacturing Ebola Vaccines to Be Tested on its
Soldiers to “Advance US Ability to Wage War”?
By Julie Lévesque
Global Research, September 20, 2014
At the beginning of August 2014 Bloomberg published an article about the “promising hopes” tobacco plants offer
“for developing an effective treatment for the deadly Ebola virus”:
Tobacco plant-derived medicines, which are also being developed by a company whose investors include Philip
Morris International Inc., are part of a handful of cutting edge plant-based treatments that are in the works for
everything from pandemic flu to rabies using plants such as lettuce, carrots and even duckweed…
Another tobacco giant-backed company working on biotech drugs grown in tobacco plants is Medicago Inc. in
Quebec City, which is owned by Mitsubishi Tanabe Pharma Corp. and Philip Morris.
Medicago is working on testing a vaccine for pandemic influenza and has a production greenhouse facility in
North Carolina, said Jean-Luc Martre, senior director for government affairs at Medicago. Medicago is planning a
final stage trial of the pandemic flu vaccine for next year, he said in a telephone interview…
Medicago ‘‘is currently closely working with partners for the production of an Ebola antibody as well as other
antibodies that are of interest for bio-defense,” he said in an e-mail. He would not disclose who the partners
were. (Ebola Tobacco Drug Joins Duckweed in Plant War on Disease, Bloomberg, August 6, 2014)
Could one of these partners be the Pentagon?
In 2009, the Defense Advanced Research Projects Agency (DARPA), part of the U.S. Department of Defense,
launched a program called Blue Angel, which some have described as “DARPA’s vaccine manufacturing challenge”.
http://www.globalresearch.ca/is-the-u-s-military-manufacturing-ebola-vaccines-to-be-tested-on-its-soldiers-to-advance-us-ability-to-wagewar/5402847
DARPA issued a press release in late July 2012 announcing they had “produced 10 million doses of an influenza vaccine in only
one month’s time.”
In a press release out of the agency’s office this week, scientists with DARPA say they’ve reach an important step in being able to
combat a flu pandemic that might someday decimate the Earth’s population. By working with the Medicago Inc. vaccine
company, the Pentagon’s cutting edge research lab says that they’ve used a massive harvest of tobacco plants to help produce a
plethora of flu-fighting vaccines.
Testing confirmed that a single dose of the H1N1 VLP influenza vaccine candidate induced protective levels of hemagglutinin
antibodies in an animal model when combined with a standard aluminum adjuvant,” the agency writes, while still noting,
though, that “The equivalent dose required to protect humans from natural disease can only be determined by future, prospective
clinical trials.”
“Vaccinating susceptible populations during the initial stage of a pandemic is critical to containment,”Dr. Alan Magill, DARPA
program manager, says in an official statement. “We’re looking at plant-based solutions to vaccine production as a more rapid
and efficient alternative to the standard egg-based technologies, and the research is very promising.” (DARPA’s Blue Angel –
Pentagon Prepares Millions of Vaccines Against Future Global Flu, RT, July 28, 2012)
This link between the U.S. military and pharmaceutical companies in the production of flu vaccines raises serious questions,
especially since the H1N1 pandemic has been exposed as a multibillion dollar fraud instigated by BigPharma and the World
Health Organization (WHO).
A stunning new report reveals that top scientists who convinced the World Health Organization (WHO) to declare H1N1 a global
pandemic held close financial ties to the drug companies that profited from the sale of those vaccines. This report, published in
the British Medical Journal, exposes the hidden ties that drove WHO to declare a pandemic, resulting in billions of dollars in
profits for vaccine manufacturers. (Mike Adams: WHO Scandal Exposed: Advisors Received Kickbacks From H1N1 Vaccine
Manufacturers, Natural News, June 7, 2010)
In 2012, it was reported that Medicago “was funded through a $21 million Technology Investment Agreement with DARPA.” (RT,
op. cit.)
http://www.globalresearch.ca/is-the-u-s-military-manufacturing-ebola-vaccines-to-be-tested-on-its-soldiers-to-advance-us-ability-to-wagewar/5402847
After investing in medical research to manufacture vaccines, the U.S Department of Defense is now sending troops to deal with a
pandemic in Africa. Is the military slowly replacing health authorities? If so, we can ask ourselves why. What is the real goal of
this “humanitarian intervention”? Maybe the answer lies in the goal of DARPA’s Blue Angel program?
In an interview last February, Blue Angel’s programme manager Dr. John Julias said:
The Blue Angel programme was launched by the US Defense Advanced Research Projects Agency (DARPA) in 2009 as a direct
response to the swine flu pandemic. The project’s goal is to improve the US’s response to pandemic influenza through accelerated
vaccine production…
The Blue Angel programme was built around the concept that the Department of Defense requires a capability to rapidly respond
to any pandemic or biological threat that jeopardizes warfighter readiness. (Chris Lo, Blue Angel: DARPA’s vaccine manufacturing
challenge, pharmaceutical-technology.com, February 10, 2014)
So the goal is “to improve the US’s response to pandemic influenza” but it is built on a concept which aims to protect “warfighters”
from “any pandemic or biological threat”, not the population in general.
Is this concept in any way related to the fact that “warfighters” instead of “health workers” are now being sent into areas affected
by the Ebola pandemic? To test a vaccine against a “biological threat that jeopardizes warfighter readiness”? Are these 3000
troops Obama is sending to Liberia being used as guinea pigs? There are precedent in this regard. This would not be the first
time.
Last February RT reported:
A federal judge has ruled the United States Army must quickly inform veterans of any potentially harmful health effects stemming
from the secret medical and drug experiments conducted on them during the Cold War.
According to a report by Courthouse News wire service, the ruling comes in favor of 7,800 soldiers claiming to have been
involved in the experiments. After recruiting Nazi scientists to help through a program called “Project Paperclip,” the Army and
CIA administered between 250 and 400 kinds of drugs to the soldiers in an attempt to advance US ability to wage war. (Judge
sides with US servicemen used as guinea pigs in terrifying Cold War experiment, RT, February 7, 2014)
http://www.globalresearch.ca/is-the-u-s-military-manufacturing-ebola-vaccines-to-be-tested-on-its-soldiers-to-advance-us-ability-to-wagewar/5402847
During the Persian Gulf War (1990-1991) experimental vaccines were also given to soldiers and several studies have concluded
that the Gulf-War Syndrome was linked to vaccinations:
Gulf-War Syndrome (GWS) refers to a collection of symptoms in soldiers who served in the Persian Gulf War (1990-1991), or
Gulf War 1. These symptoms include rash, severe fatigue, muscle and joint pain, headache, irritability, depression, unrefreshing
sleep, gastrointestinal and respiratory disorders and neurological cognitive defects.
Apart from being exposed to a wide range of environmental hazards and toxic chemicals, US and UK Gulf War I veterans
(GW1Vs) were also given large numbers of vaccines. In total, the US GW1Vs received, at least, 17 different vaccines [1] including
live vaccines (polio and yellow fever as well as experimental vaccines that had not been approved (anthrax, botulinum toxoid)
and were of doubtful efficacy [2]. In the UK, the Ministry of Defense (MoD) has declared only 10 vaccines given, but records exist
to show that some troops received a greater number [3]. Among them were two experimental vaccines, anthrax with pertussis as
an adjuvant (shown in 1990 to cause serious deconditioning in mice) [4], and plague, given to UK but not USA troops [1]. The
manufacturers of pertussis were not advised of the unlicensed use on GW1Vs [1,4].
Vaccine overload was identified as a significant factor in GWS…
These findings are consistent with those from other studies. A link between vaccinations and illness has been found among
GW1Vs from UK and Canada [6]. (Dr. Mae-Wan Ho and Prof. Malcolm Hooper Vaccines, Gulf-War Syndrome & Bio-defence)
The stated goal enunciated by Obama of the U.S. soldiers’ mission in Liberia is to build medical centers and train health workers
to operate them.
The National Institutes of Health, an agency of the U.S. Department of Health and Human Services, has already developed an
Ebola vaccine. In early September GlaxoSmithKline said it planned to begin manufacturing up to 10,000 doses of it, even though
scientists had not yet decided if “the initial vaccine was promising enough” and ”safety studies cannot guarantee that
experimental vaccines really work in an outbreak.” (Associated Press, Ebola vaccine research moving fast, CBSNews, September 8,
2014)
It is worth noting in this regard that several health hazards were in fact caused by the H1N1 vaccine. GlaxoSmithKline also
recently pleaded guilty and paid “$3 billion to resolve fraud allegations and failure to report safety data”. (GlaxoSmithKline to
Plead Guilty and Pay $3 Billion to Resolve Fraud Allegations and Failure to Report Safety Data, Department of Justice, July 2, 2014)
http://www.globalresearch.ca/is-the-u-s-military-manufacturing-ebola-vaccines-to-be-tested-on-its-soldiers-to-advance-us-ability-to-wagewar/5402847
If they (DARPA) all ready has the Ebola Vaccine, why are they stalling?
FedBizOpps.com
Could it be a consolidation of the Corporate Entity coming to pass?
https://www.fbo.gov/index?s=opportunity&mode=form&id=492773dadadb498b4829a45c7a3e7073&tab=core&_cview=0
What is Blue Angel?
In 2009, the Defense Advanced Research Projects Agency (DARPA), part of the U.S. Department of Defense,
launched a program called Blue Angel.
The project's goal is to improve the US's response to pandemic influenza through accelerated vaccine production.
The researchers specifically investigated a plant-based method of producing proteins for use in vaccines, which
has the potential to be significantly quicker than traditional egg-based production technology. The project, along
with its pharma partner Medicago, reached a major milestone in 2012, when a 'live-fire' test using tobacco-based
protein production (tobacco being favored for its ready availability and rapid growth rate) pumped out 10 million
doses of an H1N1 vaccine candidate in just one month, a major improvement over previous methods.
Blue Angel's programme :manager Dr. John Julias The US Government has made investments in programs such as
DARPA's Blue Angel and other accelerated, large-scale manufacturing efforts for medical countermeasures within
the Department of Defense and Department of Health and Human Services to develop capabilities to rapidly
respond to any emerging disease or pandemic threat…. DSO redirected a promising tobacco-plant-based protein
expression platform, initially developed under the Accelerated Manufacturing of Pharmaceuticals (AMP)
programme, to develop candidate vaccines to H1N1 at low cost and with the potential for scale up to tens of
millions of doses per month. The first component included a near-term, developmental, proof-of-concept objective
to demonstrate the safety and immunogenicity of a tobacco-plant-expressed influenza vaccine candidate protein
by conducting a Phase I human clinical trial of a recombinant H1N1 monomeric HA [haemagglutinin] vaccine
candidate.
The second component was to demonstrate a proof-of-concept, US-based capability to scale up the plant-based
expression platform technology to significantly expand the ability to produce vaccine grade recombinant protein
using phase-appropriate cGMP [current good manufacturing practice] compliant processes.
http://www.pharmaceutical-technology.com/features/featureblue-angel-darpas-vaccine-manufacturing-challenge-4171658/
CL: During a test in 2012, Medicago researchers working under Blue Angel produced 10 million doses of an H1N1
vaccine candidate in one month. How was this done?
JJ: Medicago's achievement was calculated based on a mouse model. As part of the programme goals, Medicago was
to produce at least 10 million doses of H1N1 virus-like particles (VLP) influenza vaccine candidate in a monthlong live fire test. Production of the H1N1 VLP influenza vaccine began on 25 March 2012 and was completed in
30 days on 24 April 2012. This vaccine candidate was tested in a mouse model and produced protective levels of
neutralizing antibodies.
CL: At what stage is Blue Angel today, and how has the project progressed since 2009?
JJ: The Blue Angel programme is near completion. The subunit influenza vaccine, based on recombinant
hemagglutinin from the 2009 pandemic A/California/04/2009 (H1N1) strain of influenza virus, was
manufactured using a plant virus-based transient expression technology in Nicotiana benthamiana plants and
demonstrated, in a Phase I clinical trial, to be well tolerated and immunogenic. In addition, three US-based, largescale manufacturing performers developed three different vaccine candidates and completed 30-day live-fire,
proof-of-concept exercises.
CL: What are the advantages of vaccine production using plant-based proteins rather than standard egg-based
protein production technology?
JJ: Egg-based protein production is reliant on a long lead time to procure appropriate eggs that are typically used in
seasonal influenza vaccine production. Redirecting from seasonal influenza vaccine production or procuring
additional eggs for a pandemic response can create a bottleneck in the pipeline. In addition, with some specific
influenza strains, for example avian influenza, it may be difficult to grow the vaccine in eggs. Plant-based
production overcomes some of these limitations with an ability to rapidly scale and the potential for a low-cost
economic advantage.
http://www.pharmaceutical-technology.com/features/featureblue-angel-darpas-vaccine-manufacturing-challenge-4171658/
CL: In terms of clinical trials and FDA approval, what still needs to be done to prove the efficacy and advantages of
plant-made vaccines?
JJ: Thresholds as to what criteria designate a plant-made product as safe and efficacious are determined by FDA's
regulatory review. DARPA cannot comment on the future studies that would be deemed appropriate to gain FDA
approval for plant-made vaccines.
The first plant-made biologic produced in plants was approved by the FDA in 2012 [note: this was neither funded
by DARPA nor related to Blue Angel]. Plant-based production companies, including former Blue Angel performers,
are continuing to pursue pipelines to drug approval of plant-made medical countermeasures through human
clinical studies of plant-made vaccines outside of DARPA efforts.
DARPA has funded two Phase I human clinical trials with plant-made influenza vaccine candidates under the Blue
Angel programme.
CL: Presumably, future pandemics involve unknown variables, and it's impossible to know exactly what the next
outbreak might look like. Do you think this sort of vaccine acceleration could help improve the response to novel
biological threats?
JJ: The Blue Angel programme was built around the concept that the Department of Defense requires a capability to
rapidly respond to any pandemic or biological threat that jeopardizes warfighter readiness. The tobacco-based
manufacturing platforms developed under Blue Angel have demonstrated the capability to scale up production for
any vaccine candidate, given its sequence.
http://www.pharmaceutical-technology.com/features/featureblue-angel-darpas-vaccine-manufacturing-challenge-4171658/
“Testing confirmed that a single dose of the H1N1 VLP influenza vaccine candidate induced protective levels of hemagglutinin
antibodies in an animal model when combined with a standard aluminum adjuvant,” the agency writes, while still
noting, though, that “The equivalent dose required to protect humans from natural disease can only be determined by future,
prospective clinical trials.”
Researchers have before relied on using chicken eggs to harvest compounds to use in influenza vaccines. With a future outbreak
requiring scientists to step up with a solution as soon as possible, though, they’ve turned to tobacco plants to help produce the
vaccines.
“Vaccinating susceptible populations during the initial stage of a pandemic is critical to containment,”
Dr. Alan Magill, DARPA program manager, says in an official statement. “We’re looking at plant-based solutions to vaccine
production as a more rapid and efficient alternative to the standard egg-based technologies, and the research is very promising.”
The World Health Organization has gone on the record to say that as much as half of
the people on the planet could be affected by a pandemic in the near future , and it could
take as much as nine months for a vaccine for a pandemic virus strain to become made available. With the lives of billions of
people across the world at stake, DARPA has been trying to determine new ways of churning out antidotes in as little time as
possible. Now its researchers say, that in only a month, scientists “produced more than 10 million doses (as defined in an animal
model) of an H1N1 influenza vaccine candidate based on virus-like particles (VLP).”
Through DARPA’s previously established Blue Angel program, researchers have spent several years searching for new ways to
produce mass quantities of vaccine-grade protein that could be used to combat what they say are very real emerging and novel
biological threats.
Andy Sheldon, Chief Executive Officer of Medicago , says in the company’s own press release that “The completion of the rapid
fire test marks a substantial achievement in demonstrating our technology and the potential for Medicago to be the first
responder in the event of a pandemic flu outbreak.”
Medicago’s research was conducted in a 97,000-square-foot vaccine facility in North Carolina that was funded through a $21
million Technology Investment Agreement with DARPA. http://www.globalresearch.ca/darpa-s-blue-angel-pentagon-prepares-millions-of-vaccinesagainst-future-global-flu/32141
One key ingredient in Chemtrails is Aluminum!
Even as Ebola cases multiply in West Africa, a far greater market for plant-based biopharmaceuticals will likely be influenza
vaccines used to fight pandemics, industry experts said. Making vaccines from plants may turn out to be faster and cheaper than
current methods which use chicken eggs to grow the virus needed to make the vaccines.
Leading producers such as GlaxoSmithKline Plc and Sanofi SA need six months to produce flu vaccine once scientists identify the
dominant virus expected to circulate during flu season. Vaccine production from tobacco plants by Quebec City-based Medicago
or Bryan, Texas-based Caliber Biotherapeutics could do it in weeks.
“Seven to 10 years from now, plants might be the dominant vaccine-production system,” said Brett Giroir, an MD and CEO of
Texas A&M Health Science Center in Bryan. Texas A&M has one of three US facilities tasked by the government with being ready
to produce and deliver 50mn doses of flu vaccine in just 12 weeks. It is working with Caliber toward that goal.
If the upstarts succeed, they will make little difference to the tobacco industry, which regards even a $3bn market as marginal.
But they could threaten the pharma giants that dominate flu vaccine production - or be gobbled up by them.
Medicago is now testing its flu vaccine in elderly people, who are most at risk, and
plans to launch a large human trial in 2016. “We hope to hit the market in 2019,” said
Jean-Luc Martre, director of government affairs.
http://www.gulf-times.com/Mobile/Opinion/189/details/410783/Plant-based-vaccines-challenge-big-pharma-for-$3bn-flu-market
Recently, scientists at Axis Genetics, Cambridge , have shown that injecting mink
with extracts of plants infected with a cowpea mosaic virus, that expresses a mink
enteritis antigen gene, protects the animal against subsequent virus challen26.
While much remains to be done, indications are that plant-based vaccines can
compete with vaccines produced by other approaches, particularly keeping in view
the low cost and ease of production/distribution.
Though the first report on production of edible vaccine appeared in 1990 in the
form of a patent application2 the concept of edible vaccine got impetus after
Arntzen and co-workers3 expressed Hepatitis-B surface antigen in tobacco in 1992
to produce immunologically active edible vaccine.
Advantages35
· Edible plants are very effective as a delivery vehicle for inducing oral
immunization
· Adjuvant for immune response is not necessary
· Excellent , feasibility of oral administration compared to injection
· Easy for separation and purification of vaccines from plant materials
· Effective prevention of pathogenic contamination from animal cells
· Convenience and safety in storing and transporting vaccines
· Effective maintenance of vaccine activity by controlling the temperature in plant
cultivation
· Easy for mass production system by breeding compared to an animal system
· Possible production of vaccines with low costs
· Reduced need for medical personnel and sterile injection conditions
· Economical to mass produce and transport
· Reduced dependence on foreign supply
· Storage near the site of use
· Heat stable, eliminating the need for refrigeration
· Antigen protection through bioencapsulation
· Subunit vaccine (not attenuated pathogens) means improved safety
http://www.pharmainfo.net/reviews/edible-vaccinesa-novel-approach
For all you vaccine haters out there.
Now that they have officially done away with any need for an
adjuvant!
THE #1
Edible plants are now
way to ingest a vaccine with NO metallic content, INCLUDING
MERCURY, ALUMINUM, or Flulaval contains up to 25 mcg of formaldehyde (a neurotoxin) and up to
50 mcg of sodium
deoxycholate(http://www.naturalnews.com/045418_flu_shots_influenza_vaccines_mercury.html#ixzz
3IyQbRXZ1)
Now, who is NOT going to line up for their
“vaccine” during the next Ebola outbreak!!!!
ZMapp is an experimental biopharmaceutical drug comprising three
chimeric monoclonal antibodies
ZMapp is an experimental biopharmaceutical drug comprising three chimeric
monoclonal antibodies under development as a treatment for Ebola virus
disease. The drug was first tested in humans during the 2014 West Africa Ebola
virus outbreak, but has not been subjected to a randomized controlled trial to
determine whether it works, and whether it is safe enough to allow on the
market. Like intravenous immunoglobulin therapy, ZMapp contains neutralizing
antibodies[6] that provide passive immunity to the virus by directly and
specifically reacting with it in a "lock and key“ (ENZYME) fashion.[7]. The drug is
composed of three monoclonal antibodies (mAbs) that have been chimerized by
genetic engineering.[8] The components are chimeric monoclonal antibody c13C6
from a previously existing antibody cocktail called "MB-003" and two chimeric
mAbs from a different antibody cocktail called ZMab, c2G4 and c4G7.[2]
ZMapp is manufactured in the tobacco plant Nicotiana benthamiana in the
bioproduction process known as "pharming" by Kentucky BioProcessing, a
subsidiary of Reynolds American.[1][9][10]
http://en.wikipedia.org/wiki/ZMapp
By transmutation multiple animal and plant genetic information, the chimeric
antibody can now fit with a specific enzyme into human cells. What is this specific
enzyme? More info: http://en.wikipedia.org/wiki/Monoclonal_antibody
http://en.wikipedia.org/wiki/Fusion_protein
http://www.pharmainfo.net/reviews/edible-vaccinesa-novel-approach
MB-003
MB-003 is a cocktail of three humanized or human–mouse chimeric mAbs: c13C6, h13F6 and c6D8.[2] A study published in September 2012 found
that rhesus macaques infected with Ebola virus (EBOV) survived when receiving MB-003 (mixture of 3 chimeric monoclonal antibodies) one hour
after infection. When treated 24 or 48 hours after infection, four of six animals survived and had little to no viremia and few, if any, clinical
symptoms.[12]
MB-003 was created by Mapp Biopharmaceutical, based in San Diego, with years of funding from US government agencies including the National
Institute of Allergy and Infectious Disease, Biomedical Advanced Research and Development Authority, and the Defense Threat Reduction
Agency.[1][13]
ZMAb
ZMAb is a mixture of three mouse mAbs: m1H3, m2G4 and m4G7.[2] A study published in November 2013 found that EBOV-infected macaque
monkeys survived after being given a therapy with a combination of three EBOV surface glycoprotein (EBOV-GP)-specific monoclonal antibodies
(ZMAb) within 24 hours of infection. The authors concluded that post-exposure treatment resulted in a robust immune response, with good
protection for up to 10 weeks and some protection at 13 weeks.[14]
ZMab was created by Defyrus, a Toronto-based biodefense company, funded by the Public Health Agency of Canada.[15] The identification of the
optimal components from MB-003 and ZMab was carried out at the Public Health Agency of Canada’s National Microbiology Laboratory in
Winnipeg.[16]
ZMapp
A 2014 paper described how Mapp and its collaborators, including investigators at Public Health Agency of Canada, Kentucky BioProcessing, and
the National Institute of Allergy and Infectious Diseases, first chimerized the three antibodies comprising ZMAb, then tested combinations of MB003 and the chimeric ZMAb antibodies in guinea pigs and then primates to determine the best combination, which turned out to be c13C6 from
MB-003 and two chimeric mAbs from ZMAb, c2G4 and c4G7. This is ZMapp.[2]
In an experiment also published in the 2014 paper, 21 rhesus macaque primates were infected with the Kikwit Congolese variant of EBOV. Three
primates in the control arm were given a non-functional antibody, and the 18 in the treatment arm were divided into three groups of six. All
primates in the treatment arm received three doses of ZMapp, spaced 3 days apart. The first treatment group received its first dose on 3rd day after
being infected; the second group on the 4th day after being infected, and the third group, on the 5th day after being infected. All three primates in
the control group died; all 18 primates in the treatment arm survived.[2] Mapp then went on to show that ZMapp inhibits replication of a Guinean
strain of EBOV in cell cultures.[17]
Mapp remains involved in the production of the drug through its contracts with Kentucky BioProcessing, a subsidiary of Reynolds American.[1] To
produce the drug, genes coding for the chimeric mAbs were inserted into viral vectors, and tobacco plants are infected with the viral vector
encoding for the antibodies, using Agrobacterium cultures.[18][19][20] Subsequently, antibodies are extracted and purified from the plants. Once the
genes encoding the chimeric mAbs are in hand, the entire tobacco production cycle is believed to take a few months. [21] The development of these
production methods was funded by the U.S. Defense Advanced Research Projects Agency as part of its bio-defense efforts following the 9/11 terrorist
attacks.[22][23] http://en.wikipedia.org/wiki/ZMapp
Do plants provide the correct enzyme?
Adjuvant for immune response is not necessary
Scientific background on plant-based vaccines1
Scientific advancements in plant-derived vaccines have occurred over the last decade; they include four major
milestones.
· First, insertion of genes encoding antigenic proteins of human pathogens resulted in successful expression and
assembly of multi-component structures within plant cells. These structures, which mimic the native immunogens,
include "virus-like particles" (VLPs) for the Hepatitis-B surface antigen (HBsAg), Norwalk virus capsid protein (NV
capsid), and oligomeric β-subunit of the heat labile enterotoxin of E. coli (LT-B) either by itself or in association
with the enzymatically active α-subunit to form a holotoxin (LT). (Similar studies have also been completed for
cholera toxin - CT.) Other than introduction of the genes encoding the antigens with an appropriate DNA vector
modified to optimize gene expression, no further cellular engineering of the plant cells were required to obtain
immunogens resembling the native pathogen proteins. Subsequent studies, which are continuing in other
laboratories around the world, are verifying these findings for other antigenic proteins from human and animal
pathogens.
· Second, oral immunogenicity of HBsAg, LT-B, and NV capsid was demonstrated by feeding plant material
expressing these antigens directly to animals as feed. While two of these are from enteric pathogens, which might
be anticipated to contain mucosally-active immunogens, Hepatitis-B is not an enteric pathogen and is usually not
thought to invade the body via the gut. The emerging results portend success with different types of antigens
through oral immunization, albeit with very significantly higher levels of immunogen than would be required for
injection.
http://www.pharmainfo.net/reviews/edible-vaccinesa-novel-approach
· Third, in Phase 1 human clinical trials, LT-B and NV capsid were found to stimulate both humoral and mucosal
immune responses (as evidenced by serum and mucosal antibody responses) and HBsAg gave a strong boosting
response in volunteers who had previously received the yeast-derived, injected commercial vaccine. Although the
immune responses to NV capsid was modest in amplitude, it was achieved with unprocessed plant tissues (raw
potato) with no
adjuvants, buffers or additives; in all human clinical trials, the
immunogens were active simply when the plant sample was eaten.
U.S.D.A. Approves Modified Potato http://www.nytimes.com/2014/11/08/business/genetically-modifiedpotato-from-simplot-approved-by-usda.html?_r=1
· Fourth, in unpublished studies, we have found that standard food industry freeze-drying technology can be used
for multiple plant tissues (including tomato, potato and carrot) to yield heat-stable, antigen-containing powders.
Freeze-dried tomato powder containing NV capsid and LT-B has been found to be immunogenic in pre-clinical
trials, and studies of other antigens are underway. Different batch samples can be blended to give uniform doses of
antigen and can be stored at room temperature without antigen loss.
http://www.pharmainfo.net/reviews/edible-vaccinesa-novel-approach
The Ebola Virus may have been mutated from Zaire ebola virus (strain Eckron-76)
Zaire Mayinga and Zaire-95 are the two most lethal forms of the Ebola virus, killing approximately 85% of all known
infected humans (http://biochem218.stanford.edu/Projects%202002/Doukas.pdf ). The form of Ebola virus we are
being told by Liberian Doctors is 90% lethal and is airborne is large droplets.
http://biochem218.stanford.edu/Projects%202002/Doukas.pdf
Journal of Virology May 2003: Lentivirus Vectors Pseudotyped with Filoviral Envelope Glycoproteins Transduce
Airway Epithelia from the Apical Surface Independently of Folate Receptor Alpha
Abstract
The practical application of gene therapy as a treatment for cystic fibrosis is limited by poor gene transfer
efficiency with vectors applied to the apical surface of airway epithelia. Recently, folate receptor alpha (FRα), a
glycosylphosphatidylinositol-linked surface protein, was reported to be a cellular receptor for the filoviruses. We
found that polarized human airway epithelia expressed abundant FRα on their apical surface. In an attempt to
target these apical receptors, we pseudotyped feline immunodeficiency virus (FIV)-based vectors by using envelope
glycoproteins (GPs) from the filoviruses Marburg virus and Ebola virus. Importantly, primary cultures of welldifferentiated human airway epithelia were transduced when filovirus GP-pseudotyped FIV was applied to the
apical surface. Furthermore, by deleting a heavily O-glycosylated extracellular domain of the Ebola GP, we
improved the titer of concentrated vector severalfold. To investigate the folate receptor dependence of gene transfer
with the filovirus pseudotypes, we compared gene transfer efficiency in immortalized airway epithelium cell lines
and primary cultures. By utilizing phosphatidylinositol-specific phospholipase C (PI-PLC) treatment and FRαblocking antibodies, we demonstrated FRα-dependent and -independent entry by filovirus glycoproteinpseudotyped FIV-based vectors in airway epithelia. Of particular interest, entry independent of FRα was observed
in primary cultures of human airway epithelia. Understanding viral vector binding and entry pathways is
fundamental for developing
cystic fibrosis gene therapy applications.
What does Cystic Fibrosis, Ebola, and Obama July 31, 2014, “Quarantinable
communicable diseases revised executive order, have in common?
How many asthmatics were misdiagnosed (http://cpj.sagepub.com/content/26/2/78.short ;
http://www.rightdiagnosis.com/c/cf/misdiag.htm ) as a child and should have been tested for Cystic Fibrosis?
Probably millions. Almost all asthmatics, numerous times in their life, became ill, went to the doctor with shortness
of breath, coughing, was diagnosed with Bronchitis or similar infection and was given a round of antibiotics. This
very procedure stemmed the tide of understanding a deeper problem going on with asthma patients and their
constant lung and nasal infections. Unbeknownst to them that they were not suffering from asthma, but Cystic
Fibrosis.
The only known cure for Cystic Fibrosis (CF) currently is to treat the secondary bacterial infections that build up
from time to time in the lungs and nasal passages with antibiotics. Other drugs exist that help a small percentage
of CF suffers, but a cure is not known.
Cystic fibrosis (CF) is a life-threatening genetic disease that primarily affects the lungs and digestive system. An
estimated 30,000 children and adults in the United States (70,000 worldwide) have CF.
In people with CF, a defective gene and its protein product cause the body to produce unusually thick, sticky mucus
that:
Clogs the lungs and leads to life-threatening lung infections.
Obstructs the pancreas and stops natural enzymes from helping the body break down food and absorb vital
nutrients. http://www.cff.org/AboutCF/
http://www.whitehouse.gov/the-press-office/2014/07/31/executive-order-revised-list-quarantinable-communicable-diseases
All in all, Cystic Fibrosis is a respiratory disease and therefore quarantinable under the Obama Executive order
13295 in the event of a pandemic as would be Asthmatics.
Here’s where this gets interesting. Why “Severe Acute Respiratory Syndromes?”
Section 1. Amendment to Executive Order 13295. Based upon the recommendation of the Secretary of Health and Human Services, in consultation
with the Acting Surgeon General, and for the purposes set forth in section 1 of Executive Order 13295 of April 4, 2003, as amended by Executive
Order 13375 of April 1, 2005, section 1 of Executive Order 13295 shall be further amended by replacing subsection (b) with the following:
"(b) Severe acute respiratory syndromes, which are diseases that are associated with fever and signs and symptoms of pneumonia or other
respiratory illness, are capable of being transmitted from person to person, and that either are causing, or have the potential to cause, a pandemic,
or, upon infection, are highly likely to cause mortality or serious morbidity if not properly controlled. This subsection does not apply to influenza
(http://www.whitehouse.gov/the-press-office/2014/07/31/executive-order-revised-list-quarantinable-communicable-diseases ).“
The Ebola Virus, now a patented hybrid strain of Zaire-95, the O-glycosylated Delta-peptide is officially being
used to find a “cure” for Cystic Fibrosis.
Hitler’s experimenting on human beings did
not end in WW2, but just went underground
for a time.
http://www.brettrussell.com/personal/what_are_the_chances_.html
Evidence of airborne transmission of Ebola Zaire between animals presented in a
scientific paper in 2012. The authors wrote that “Segmental attenuation and loss of
respiratory epithelium in the bronchiolar wall (large arrow) with some areas of the
lungs relatively unaffected (arrowhead). Immunostaining for Ebola virus antigen
was detected in occasional respiratory epithelial cells (small arrow) as well as
within alveolar and septal macrophages. Bar = 50 μm.” Courtesy: authors and
Scientific Reports.
Scientific paper on airborne Ebola transmission: Transmission of Ebola virus from pigs to non-human primates by
Hana M. Weingartl, Carissa Embury-Hyatt, Charles Nfon, Anders Leung, Greg Smith & Gary Kobinger published in
Scientific Reports 2,Article number:811 doi:10.1038/srep00811
Ebola viruses (EBOV) cause often fatal hemorrhagic fever in several species of simian primates including human.
While fruit bats are considered natural reservoir, involvement of other species in EBOV transmission is unclear. In
2009, Reston-EBOV was the first EBOV detected in swine with indicated transmission to humans. In-contact
transmission of Zaire-EBOV (ZEBOV) between pigs was demonstrated experimentally. Here we show ZEBOV
transmission from pigs to cynomolgus macaques without direct contact. Interestingly, transmission between
macaques in similar housing conditions was never observed. Piglets inoculated oro-nasally with ZEBOV were
transferred to the room housing macaques in an open inaccessible cage system. All macaques became infected.
Infectious virus was detected in oro-nasal swabs of piglets, and in blood, swabs, and tissues of macaques. This is the
first report of experimental interspecies virus transmission, with the macaques also used as a human surrogate. Our
finding may influence prevention and control measures during EBOV outbreaks.
http://leonclifford.com/2014/08/01/who-chief-warns-of-ebola-mutation-risk/
Some facts about this
Ebola strain and outbreak
2014.
In a study done by Tulane University, the Broad Institute and Harvard University, in partnership with the Sierra
Leone Ministry of Health and Sanitation, researchers may have provided information about the origin and
transmission of the Ebola virus that sets this outbreak apart from previous outbreaks. For this study, 99 Ebola virus
genomes were collected and sequenced from 78 patients diagnosed with the Ebola virus during the first 24 days of
the outbreak in Sierra Leone. From the resulting sequences, and three previously published sequences from Guinea,
the team found 341 genetic changes that make the outbreak distinct from previous outbreaks. It is still unclear
whether these differences are related to the severity of the current situation.[125] Five members of the research team
became ill and died from Ebola before the study was published in August.[125]
http://en.wikipedia.org/wiki/Ebola_virus_epidemic_in_West_Africa
This piece of information came from #125 citation of ScienceMag.org, Aug. 28, 2014
http://www.sciencemag.org/content/345/6202/1369
“This West African variant likely diverged from central African lineages
around 2004, crossed from Guinea to Sierra Leone in May 2014, and has
exhibited sustained human-to-human transmission
(http://www.sciencemag.org/content/345/6202/1369.full ).”
The 2004, according to the WHO, outbreak came from Sudan. The current
outbreak started in February 2014 in Guinea, West Africa(S. Baize et al.,
Emergence of Zaire Ebola virus disease in Guinea—Preliminary report. N.
Engl. J. Med. 10.1056/NEJMoa1404505 (2014).), and spread into Liberia
in March, Sierra Leone in May, and Nigeria in late July. It is the largest
known EVD outbreak and is expanding exponentially, with a doubling
period of 34.8 days.
http://www.who.int/mediacentre/factsheets/fs103/en/
“Our data suggest that the Sierra Leone outbreak stemmed from the
introduction of two genetically distinct viruses from Guinea around the
same time. Samples from 12 of the first EVD patients in Sierra Leone, all
believed to have attended the funeral of an EVD case from Guinea, fall into
two distinct clusters (clusters 1 and 2) (Fig. 4A and fig. S8). Molecular
dating places the divergence of these two lineages in late April (Fig. 3B),
predating their co-appearance in Sierra Leone in late May (Fig. 4B); this
finding suggests that the funeral attendees were most likely infected by
two lineages then circulating in Guinea, possibly at the funeral (fig. S9).
All subsequent diversity in Sierra Leone accumulated on the background
of those two lineages (Fig. 4A), consistent with epidemiological
information from tracing contacts….” “In memoriam: Tragically, five coauthors, who contributed greatly to public health and research efforts in
Sierra Leone, contracted EVD and lost their battle with the disease before
this manuscript could be published: Mohamed Fullah, Mbalu Fonnie, Alex
Moigboi, Alice Kovoma, and S. Humarr Khan. We wish to honor their
memory. ” (http://www.sciencemag.org/content/345/6202/1369.full ). ‘
http://www.sciencemag.org/content/345/6202/1369
Fig. 1 Ebola outbreaks, historical and current.(A) Historical EVD outbreaks, colored by decade.
Ebola outbreaks, historical and current.(A) Historical EVD outbreaks, colored by decade. Circle area represents total number of
cases (RC = Republic of the Congo; DRC = Democratic Republic of Congo). (B) 2014 outbreak growth (confirmed, probable, and
suspected cases). (C) Spread of EVD in Sierra Leone by district. The gradient denotes number of cases; the arrow depicts likely
direction. (D) EBOV samples from 78 patients were sequenced in two batches, totalling 99 viral genomes [replication = technical
replicates (6)]. Mean coverage and median depth of coverage with range are shown. (E) Combined coverage (normalized to the
sample average) across sequenced EBOV genomes.
Published by AAAS
S K Gire et al. Science 2014;345:1369-1372
What is BEAST dating and analysis?
Notice the Octopus!
http://beast.bio.ed.ac.uk/tutorials
BEAST Software - Bayesian Evolutionary
Analysis Sampling Trees
BEAST is a cross-platform program for Bayesian analysis of
molecular sequences using MCMC. It is entirely orientated
towards rooted, time-measured phylogenies inferred using strict
or relaxed molecular clock models. It can be used as a method of
reconstructing phylogenies but is also a framework for testing
evolutionary hypotheses without conditioning on a single tree
topology. BEAST uses MCMC to average over tree space, so that
each tree is weighted proportional to its posterior probability.
We include a simple to use user-interface program for setting
up standard analyses and a suit of programs for analyzing the
results.
http://beast.bio.ed.ac.uk/
The Octopus in Luciferian symbolism.
"The real menace of our Republic is the invisible Government which like a giant Octopus, sprawls its slimy legs
over our cities, states, and nation". - John F. Hylan - Mayor NYC 1918-1925
THE OCTOPUS: A SYMBOL OF GLOBAL
CONTROL
Let's not forget that aisles were placed in
the stadium that illustrated the British
"Union Jack" flag.
In the closing ceremonies, each line of the
British flag was gripped by the tentacles of
a vast, psychedelic octopus. It is also
important to note that each line of the flag
was also covered with newspaper-style text
while this happened -- clearly indicating a
relationship with the print media. In the
last image, we see that one key headline,
positioned directly next to the octopus, says
"When a man is tired of London, he is tired
of life.“ The overall message here seems to
be celebrating the octopus-like control the
Cabal has exercised over the media -- and
by extension, the world. Notice also how
the dancers end up completely lying flat on
their bellies in front of the octopus -prostrating themselves in supplication to
the great beast. http://divinecosmos.com/start-here/davids-blog/1074-olympicsilluminati
Aristotelian Biology
The ancient Greek philosopher
was the first scientist.
By Armand Marie Leroi |
September 1, 2014 http://www.thescientist.com/?articles.view/arti
cleNo/40852/title/AristotelianBiology/
https://seeker401.files.wordpress.com/2012/06/bilderberg.jpg
Could Mandatory Vaccines come in 2015?
http://marketdailynews.com/2014/08/05/all-americans-will-have-to-take-an-ebola-vaccine/
http://fas.org/sgp/crs/misc/RS21414.pdf
http://fas.org/sgp/crs/misc/RS21414.pdf
The Model Act
http://fas.org/sgp/crs/misc/RS21414.pdf
http://en.wikipedia.org/wiki/Model_act
http://www.whitehouse.gov/the-press-office/2014/07/31/executive-order-revised-list-quarantinablecommunicable-diseases
The Military has been forcing vaccinations on it’s soldiers
for decades.
http://fas.org/sgp/crs/misc/RS21414.pdf
http://www.nvic.org/nvic-vaccine-news/february-2014/2014-state-vaccine-legislation-in-america---battle.aspx
http://www.nvic.org/nvic-vaccine-news/february-2014/2014-state-vaccine-legislation-in-america---battle.aspx
http://www.nvic.org/nvic-vaccine-news/february-2014/2014-state-vaccine-legislation-in-america---battle.aspx
http://www.nvic.org/vaccine-laws/tracking-system-and-privacy/the-national-electronic-tracking-registry.aspx
1905 Supreme Court Speaks
In 1905, a man named Jacobsen and his son sued the state of Massachusetts for requiring them to get a second smallpox
vaccination or pay a $55 fine. Jacobsen refused to get re-vaccinated or pay the fine, claiming he and his son had had a bad
reaction to a previous smallpox vaccination and were afraid they would be injured or die by a second one. Jacobsen maintained
that forcing him to be revaccinated was "an assault upon his person" and violated his Constitutional rights.
The Supreme Court rejected the evidence Jacobsen presented to show that the smallpox vaccination can cause injury and death
and to demonstrate that doctors cannot distinguish between those who will be harmed and those who won't be harmed by the
vaccination. The Court concluded "The matured opinions of medical men everywhere, and the experience of mankind, as all must
know, negate the suggestion that it is not possible in any case to determine whether vaccination is safe."
Doctors Cannot Predict Who Will Become Vaccine Injured
The fact that the nine Supreme Court justices at the turn of the century did not have accurate medical information upon which to
base their precedent-setting decision is as understandable as it is unfortunate. It has been proven in the succeeding 94 years, most
recently in the U.S. Claims Court in Washington, D.C., where more than 1 billion dollars has been awarded to some 1,000
American families, whose children have died or been injured from the adverse effects of childhood vaccines, that often doctors
cannot predict ahead of time which children will react to vaccines, die or be left with mental retardation, medication-resistant
seizure disorders, learning disabilities, chronic arthritis, paralysis or other immune deficiencies and brain damage.
Doctors Don’t Respect Biodiversity or Report Vaccine Reactions
Between 12,000 and 14,000 reports of hospitalizations, injuries and deaths following vaccination are made to the government's
Vaccine Adverse Events Reporting System (VAERS) every year. Yet, it is estimated that fewer than one to 10 percent of all doctors
report serious health problems which occur following drug or vaccine administration.
The fact that genetic and other as yet unidentified biological factors can place some individuals at higher risk for vaccine-induced
injury and death calls into question the constitutionality of a one-size-fits-all forced vaccination policy that does not take into
account individual biological differences. This is a critical point in measuring the consequences of assigning police powers to
public health officials for the purpose of enforcing vaccination, particularly in cases where parents suspect their children are at
increased risk for reacting to vaccines even though health officials, anxious to achieve a 100 percent vaccination rate, disagree.
http://www.nvic.org/vaccine-laws/tracking-system-and-privacy/the-national-electronic-tracking-registry.aspx
http://www.nvic.org/vaccine-laws/tracking-system-and-privacy/the-national-electronic-tracking-registry.aspx
http://www.nvic.org/vaccine-laws/tracking-system-and-privacy/the-national-electronic-tracking-registry.aspx
http://www.nvic.org/vaccine-laws/tracking-system-and-privacy/the-national-electronic-tracking-registry.aspx
http://www.nvic.org/vaccine-laws/tracking-system-and-privacy/the-national-electronic-tracking-registry.aspx
http://www.nvic.org/vaccine-laws/tracking-system-and-privacy/the-national-electronic-tracking-registry.aspx
http://www.nvic.org/vaccine-laws/tracking-system-and-privacy/the-national-electronic-tracking-registry.aspx
http://www.nvic.org/vaccine-laws/tracking-system-and-privacy/the-national-electronic-tracking-registry.aspx
http://www.nvic.org/vaccine-laws/tracking-system-and-privacy/the-national-electronic-tracking-registry.aspx
http://www.nvic.org/vaccine-laws/tracking-system-and-privacy/the-national-electronic-tracking-registry.aspx
http://www.nvic.org/vaccine-laws/tracking-system-and-privacy/the-national-electronic-tracking-registry.aspx
http://www.nvic.org/vaccine-laws/tracking-system-and-privacy/the-national-electronic-tracking-registry.aspx
Vaccines are AGAINST Yahweh’s Laws!
23 vaccines contain cells, cellular debris, protein, and DNA from aborted babies, including: Adenovirus, Polio,
Dtap/Polio/HiB Combo, Hep A, Hep A/Hep B Combo, MMR, MMRV Pro Quad, Rabies, Varicella, and the Shingles
vaccines.
Are you a Christian and holding a Pro-Life sign on Sunday, then vaccinating your kids on Monday –
HYPOCRITES!!!!
“We’re talking about Christianity here, which means we believe in the sixth
commandment, “Thou shalt not murder (Exodus 20:13 & Deuteronomy 5:13).”
Children are recognized from God at the point of conception (Genesis 4:1, 17,
and Jeremiah 1:5), are knit together by God in the womb (Psalm 139:13-16; Psalm
22:10-11; & Galatians 1:15), are blessings from God (Genesis 1:28; Genesis 4:1; and
Psalms 127:3 and 113:7-9), are valued and loved (Matthew 18:1-14 and 19:13-15),
are created in His image (Genesis 1:27), and their killing is condemned (Psalm 106:35,
37-38). In fact, the prophet Amos condemns the Ammonites because they “ripped
open expectant mothers in Gilead” (Amos 1:13) and child killing was one of the major
reasons that God’s anger burned against the Kingdom of Israel bringing about their
destruction and exile (2 Kings 17:17-18) (http://www.livingwhole.org/god-does-notsupport-vaccines/).”
Oh, but they only use cell lines from two aborted babies in the vaccines and the benefit to the public as a whole is
far outweighed. False times deuce. First of all, sacrificing the few for the many is biblically unjustifiable. God
prohibits child sacrifice (Exodus 20:13, Deuteronomy 5:13, 12:30-32, 18:10, Leviticus 18:21 & 20:2-5, 2 Kings
16:3, and Psalm 106:38), and there is no “for the greater good clause” or “public exception” listed in anywhere in
the Bible.
Secondly, even though there are only baby parts from a few babies in our vaccines, many more babies were aborted
and dissected in the process of obtaining the perfect strain. In fact, aborted babies are being used everyday to create
new cell lines for more vaccines. But just in case you didn’t hear this on the news, in church, or at your doctor’s
office, here’s where these ground up baby parts came from:
PER C6 came from a healthy 18 week-old baby who was aborted for social reasons. This tumorigenic strain is
being used to develop adenovirus, Ebola, influenza, malaria, tuberculosis, and HIV vaccines. Developers call it a
“human designer cell” but what they really mean is “aborted baby cells.”
The HEK293 cell line is derived from the kidneys of a healthy aborted fetus and is being used to develop new
influenza vaccines.
WI-38 (RA 27/3) was a 16-week-old female baby (20 cm long) who was aborted in Sweden because the parents
felt they had too many children. The baby was packed on ice and sent to the United States (speculation suggests
without consent – which was common) where it was dissected. The use of WI-38 cells is a lucrative moneymaking
business.
WI-1 through WI-25 cell strains were derived from the lung, skin, muscle, kidney, heart, thyroid, thymus, and liver of 21
separate elective (and some speculate illegal) abortions.
WI-27 was the fetus from which researchers extracted the live virus used in the rubella vaccine.
WI-44 was derived from the lung of a three-month old surgically aborted fetus.
MCR-5 cell line was derived from the lung tissue of a 14-week-old male (Britain).
Eighty elective abortions (recorded) were involved in the research and final production of the current rubella vaccine: 21 from
the original WI-1 through WI-26 fetal cell lines that failed, plus WI-38 itself, plus 67 from the attempts to isolate the rubella
virus.
http://www.livingwhole.org/god-does-not-support-vaccines/
People will tell you that there aren’t actually any “aborted fetal ingredients” in the final product (as
if that matters) that it’s just a medium used in the process. They say things like:
The vaccine that you are offered today contains no trace of the cells that the first-ever batch was grown
on.
So…they’re saying it’s like homeopathy? So…its just “frequency” of dead baby? Isn’t that pseudoscience?
Despite what you’ve been told, aborted baby goodies are in your vaccinations and it says so right in the
package inserts:
This product also contains residual components of MRC-5 cells including DNA and protein (pages 6-7
Varivax insert).
Human safety studies on the effects of aborted fetal DNA, cells, and proteins? Zero. But there is research
that shows that the mixing of DNA in the vaccine and DNA in your child could be one of the many ways
vaccines contribute to cancer and autism. (See how I did that? Implicated vaccines as a contributing factor
in autism without even mentioning mercury?)
And, the DNA from neoplastic cells can contain activated (cancer-causing) oncogenes, viral oncogenes,
the genomes of oncogenic viruses, as well as retroviruses that can be transferred to vaccine recipients
potentially inducing tumors. Don’t worry though; your pharmaceutical company will take extra precautions
(like they did with the Polio vaccine) to make sure this doesn’t happen.
Hello? What are we doing? There is no religious justification that makes it even remotely okay to play
“operation” with an aborted baby, let alone inject our children with foreign human DNA that has the
propensity to cause all sorts of medical conditions.
http://www.livingwhole.org/god-does-not-support-vaccines/
It’s Not Just About the Babies
It’s not just the aborted baby parts you should have an objection to. Neurotoxins, hazardous substances,
attenuated viruses, animal parts, foreign DNA, albumin from human blood, carcinogens, and chemical
wastes are all ingredients in your child’s vaccinations and not one of them are proven safe.
Not…a…single…one.
“Do you not know that your bodies are temples of the Holy Spirit, who is in you, whom you have received
from God? You are not your own; you were bought at a price. Therefore honor God with your bodies (1
Corinthians 6:19-20, NIV).
“So, whether you eat or drink, or whatever you do, do all to the glory of God (1 Corinthians 10:31)”
And then there’s the issue of contamination. Not only are the additives in vaccines considered
contaminants from a biblical standpoint, the contaminants themselves are often contaminated (making
them unavoidably unsafe).
Since vaccine preparation involves the use of materials of biological origin, vaccines are subject to
contamination by micro-organisms. […] The increasing number of target species for vaccines, the diversity
of the origin of biological materials and the extremely high number of known and unknown viruses and
their constant evolution represent a challenge to vaccine producers and regulatory authorities.
In the Bible, blood represented the life force of the human or animal. Human blood was to be kept pure
under all circumstances and free of contaminants like animal parts and blood (Genesis 9:4, Leviticus
17:11, 17:14, Deuteronomy 12:23, Leviticus 17:10, Acts 15:20, and Acts 15:29).
http://www.livingwhole.org/god-does-not-support-vaccines/
Bovine cow serum for example, is often contaminated with viruses that cause viral diarrhea. In 2012, Merck recalled over a
million doses of their PedVaxHib (Hib vaccine) and ComVax HiB/Hepatitis B combination vaccine because of Bacillus Cereus
contamination, a bacteria that typically causes diarrhea and food poisoning. The polio vaccines used in the 1950’s and 60’s were
contaminated by the SV40 virus from monkey kidney cells now responsible for several different types of cancer including brain
and bone cancer, lymphomas, leukemia, and mesothelioma, and can be passed to subsequent generations via maternal antibodies
from those vaccinated with contaminated vaccines.
Even the CDC admitted SV40 was an oopsie on their website…and then the page was removed. Don’t worry though, those
aborted baby and tumor-derived cell lines only cause cancer if they’re contaminated, and those crazy lab-viruses only cause
harm if they “escape” from a lab. Rest assured, your pharmaceutical company has everything under control.
Moreover, laboratory safety practices and technology cannot erase human error and equipment failures that lead to accidents, as
evidenced by a recent string of lab-acquired infections and environmental releases of SARS, Ebola, tularemia, and other
dangerous diseases. In fact, the last reported human cases of smallpox were laboratory acquired.
But wait, what about my neighbor?
Apparently, I owe my neighbor a Christian duty to get vaccinated…but you see, I don’t owe my neighbor any duty that conflicts
with God’s Word. After God, I owe a duty to my child, not your child…and my child is not getting vaccinated.
Yeah, but the Bible says you have to submit to governing authority.
Remember the whole…”Thou shalt have no other Gods thing?” Oh yeah…that. We Christians are not to
submit to any governing authority or policy that is not submissive to God’s Word (Book of Daniel, Esther
4:11 – 7:3, Acts 5:27-29, 1 John 2:4), are to “have no other gods,” are to keep God’s commands even in
the face of policy that forbids it (Daniel 6:7-10), and are not to defile ourselves with things of
the culture that contradict our God (Daniel 1:8).
http://www.livingwhole.org/god-does-not-support-vaccines/
Biblical support for those who wish to avoid vaccinations for spiritual and religious reasons include the following
law prohibiting genetic engineering or the use of its products:
Leviticus:19:19 Ye shall keep my statutes. Thou shalt not let thy cattle gender with a diverse kind: thou shalt not
sow thy field with mingled seed: neither shall a garment mingled of linen [plant] and woolen [animal] come upon
thee.
Relevant reasons for God's warning in this regard includes the fact that bovine (cow) fetal serum is commonly used
in the manufacturing process of vaccines. So are monkey kidney cells, chicken embryo parts, bacterial or viral
genetic materials - RNA and DNA, as well as yeast and human proteins. Using the example of cows, bovine fetal
serum is mixed with bacteria or viral particles, and other vaccine ingredients including toxic metals, such as
mercury and aluminum, and immune destructive chemicals. Thus, proteins and genetic materials from the cattle,
viruses, and bacteria are mixed before these particles are injected into you or your children. Once the vaccine
ingredients, including foreign RNA and DNA, and genetically engineered bacteria and/or viruses, or their parts,
enter your blood, they may cause genetic mutations of your cells. Then you have sown thy bloodstream 'with
mingled seed' that not only taxes your immune system further, but may cause the development of cancer cells as
well. These may go on to become full blown cancers, particularly in the presence of a weakened immune system
made weak by vaccine 'adjuvents.'
http://www.tetrahedron.org/articles/vaccine_awareness/Vaccination_UnGodly_Practice.html
Given this alarming background, the following Bible passages have special relevance:
Lamentations 4.13-15 foreshadows the AIDS pandemic, and other current and coming plagues. It also relays the fear and
avoidance surrounding HIV-positive and other infected, sick, and dying people. As you read the first paragraph, consider the fact
that religious leaders are encouraging their followers to get vaccinated. Many are even inviting 'public health' nurses and vaccine
administrators into their congregations to deliver the toxic, and too often lethal, doses:
"It happened because of the sins of her prophets and the offenses of her priests (and rabbis), who, within her walls, shed the blood
of the righteous. They wander in the streets like the blind; they are so polluted with blood that nobody is able even to touch their
clothing. Keep away! Unclean!' people shout at them, 'Keep away! Away, don't touch us!' They flee, to wander here and there; but
no nation allows them to stay."
Ezekiel 3:18-20 provides a pretty good argument why it's important to relay these facts concerning vaccines, blood transfusions,
sin, and death:
"When I say to a wicked man, 'You will surely die,' and you do not warn him or speak out to dissuade him from his evil ways in
order to save his life, that wicked man will die for his sin, and I will hold you accountable for his blood. But if you do warn the
wicked man and he does not turn from his wickedness or from his evil ways, he will die for his sin; but you will be saved
yourself."
Ezekiel 5.17 provides another blood-related warning and prophecy that may relate to recent outbreaks,
particularly the hemorrhagic fever virus Ebola. As documented in the book "Emerging Viruses: AIDS & Ebola- Nature,
Accident or Intentional?," this virus was apparently produced by Litton Bionetics - America's sixth leading biological weapons
contracting laboratory:
"Yes, I will send famine and savage beasts upon you to leave you without children; plague and bloodshed will sweep through you;
and I will bring the sword upon you. I, God, have spoken it."
Luke 13.1-5 states that those who mix human blood with the blood of sacrificed animals are 'sinners.' This is precisely what
pharmaceutical industrialists do to many vaccines.
"There were present at that season some that told him of the Galileans, whose blood Pilate had mingled with their sacrifices. And
Jesus answering said unto them. Suppose ye that these Galileans were sinners above all the Galileans, because they suffered such
things?"
http://www.tetrahedron.org/articles/vaccine_awareness/Vaccination_UnGodly_Practice.html
Finally, Revelation provides an 'End Times' prophecy in which the Kings, merchants, and wealthiest men
of all the nations were deceived by 'magic spells' or 'sorcery.' Biblical references to the practice of 'magic
spells' or 'sorcery' comes from the Greek root word of 'sorcery,' that is, pharmacopeia meaning
pharmacy. This 'sorcery,' is not only associated in the Bible with spilled and impure blood, but with the
great plagues, and onslaught of deadly 'beasts.'
Strong's Concordance Root word for 'beasts' is the 'Hebrew word #2416- chay- alive, raw flesh . . .
appetite; in the Greek Lexicon, the Greek word #2342 for 'beasts' is 'therion'- 'a little beast, little animal.'
Thus, the earth's greatest depopulation event is predicted to be associated with little beasts and the great
plagues. Could these 'little beasts' be bacteria, viruses, and pieces thereof- infectious microorganisms
most insidiously spread throughout the world, most precisely and extensively, in contaminated blood
and vaccines? That's exactly what many experts say is occurring today.
Those who 'fornicated' with the devil, and stole 'the blood of prophets and of God's people,' would surely
be severely judged by God in the last days. (See Revelation 18:23-19:2.) The Bible predicts that around
the time 'Babylon the great' falls, its deadly wine, also symbolic of blood, will flow out full of impurities
into the 'rivers and streams' that the Bible says are the earth's 'people.' They will likely then be infected
with agents- little 'beasts'- associated with great plagues that will wipe out more than a third of the
world's population.
http://www.tetrahedron.org/articles/vaccine_awareness/Vaccination_UnGodly_Practice.html
The CDC, Governments, United
Nations, Etc… are USURPING
our ability to fight against
Vaccinations biblically by
illuminating the need for
adjuvants in vaccines!!!
Extropianism is the foremost version of transhumanism. While all transhumanists as such will agree on many overall goals, they
may differ over the principles that will get us to a posthuman stage. The philosophy of Extropianism affirms the values of
Boundless Expansion, Self-Transformation, Dynamic Optimism, and Intelligent Technology, and Spontaneous Order. All of
Western Civilization is based upon the premise of “Natural Rights”. The implication that Natural Law is an inescapable component
of individual purpose and social conduct is central to a cosmology of a grand design. The pursuit of understanding does not have
to adopt a deist revelation in order to advocate a rational limitation on the human being. However, a belief in a divine creator is
the very foundation of our common heritage and traditional culture.
The frontiers of Transhumanism scorns empiricism. The eupraxophy objective is to deny an external divinity, while professing to
become gods in the process of honing their nanotechnology and neuropharmacology perfection. If Extropianism is possible, there
is no need for a God Creator.
David Lawrence III, the editor of StrategicNews.com pens a provocative treatise called THE ELIJAH OPTION.
The religious argument based upon the oral and written biblical record stems from an acknowledgement on the fallen nature of
man. Even the most optimistic extropian transhumanist cannot deny the dismal documentation of man’s inhumanity to man. Evil
is real and this fact permeates every aspect of social and metaphysical experience.
Mr. Lawrence succinctly states the axiomatic, that every Christian should know and freely accept.
“God Almighty has no intention of helping man to install any kind of permanent command and control system for the
management of evil, and it is monotheistic madness for any believer in the God of Abraham to attempt otherwise. The entire
purpose of the experiment on planet earth was to prove that evil does not work, and that we cannot live apart from Him. The
moral law of the Almighty Creator is just as immutable as the natural laws that govern the universe. It cannot be broken.”
Transhumanism that rests upon a eupraxsophy of humanistic convictions that has no boundary of restrains, is erroneous.
Wikipedia cites that the Ukrainian/Russian existentialist philosopher, Lev Shestov developed his reputation as an original and
incisive thinker, In All Things Are Possible. Shestov adopted the aphoristic style of Friedrich Nietzsche and dealt with such issues
as religion, rationalism, and science. His discovery of Kierkegaard prompted Shestov to realize that he shared great similarities,
such as his rejection of idealism, and his belief that man can gain ultimate knowledge through ungrounded subjective thought
rather than objective reason and verifiability. The artificial ultraintelligent Overman, sees no need to seek this outside help to
achieve the ultimate paragon. Thus lays the fatal flaw in the hubris of the nihilism that fixates upon the same arrogance of
Lucifer. (http://www.veteransnewsnow.com/2014/09/30/nwo-overman-eupraxsophy-transhumanism/).”
The sanctity of the individual created human soul is synonymous within all beliefs in God. It is symptomatic of the Totalitarian
Collectivism that dominates the drive to delink man’s – Similarity, Community, Values and Human Nature – that promotes the
Transhumanism dialectic.
The Elijah Option resolves,
“Mankind is on a collision course with destiny. The only thing that is not yet decided is the fate of each individual soul. Mankind
will attempt to save itself, and in so doing, build the new world-wide city of Babylon, in defiance of the Almighty who declares
that mankind will never succeed in the self-management of its own evil.”
Only a dullard believes that the insolvable global chaos is reversible through conventional means. Conversely, the Transhumanist
readily professes that the New World Order fosters this disorder to further their migration away from the sub species that serves
this new class of genetic Übermensch. The pitiful deniers that relinquish their Inherent Autonomy to this posthuman man-beastrobot entity, become not mere tools for their new masters, but actually provide no useful purpose for their continued existence.
With a pretended sense of mercy and compassion the Transhuman eugenicists deems justified, their self-convinced supreme right
in their own divinity. The irony that their secular humanism claim of not being a religion, begs the practice of a devotion to rule
over the inferior human descendents that did not make the leap into the immortal realm.
The essential question remains. Will the Transhuman have a soul in addition to their cyberspace matrix? Can a soul be created by
an Extropianist or is a soul unnecessary baggage, when secular Transhumanism become the dominate ethic?
Sure preposterous postulations are reminiscent of the Genesis account in the rebellion of the cherub. Beelzebub goes high tech
with the assistance of government research funding.
Britt Gillette of End Times Bible Prophecy referenced by Mr. Kovacs WND article, accordingly.
“Taken in its original context, Jesus did not necessarily say that unless those days are shortened, “humanity will not survive.”
Instead, he said unless those days are shortened, “no flesh will survive.”
If the transhumanist movement succeeds in transforming the human race into a race of “posthumans” who no longer need flesh
covered bones to survive, then these words of Jesus take on an entirely different meaning.
And it doesn’t take an illogical leap of faith to draw this conclusion.
http://www.veteransnewsnow.com/2014/09/30/nwo-overman-eupraxsophy-transhumanism/
After all, it seems reasonable to assume that humanity will have to undergo some sort
of radical transformation in order to plot a war against God Almighty. The arrogant
impulse already exists. All that remains is the need for an exponential increase in
human power which deludes humanity into believing it can overcome the Lord of
lords.”
Sounds like a Transhuman Satan featured in the final cut of the actual Apocalypse
Now redux, waging an Armageddon in hopes of a different result. The New World
Order has a decisive objective. The total subjugation of humanity is only a stage,
leading to the elimination of all God fearing believers. The deification of
substitute gods endowed by posthuman powers that overshadows Yahweh wants
engineered Elohim clones.
The end of this age is rapidly approaching. What follows does not bode well for
humanity under the reign of a Transhumanism world. Salvation for our created
human beings from the evil transgressions of the Overman’s hubris requires our
humbling before our Lord and Creator. Faith and belief is the alternative to
malevolence and despair. Hope in providential intervention is intellectually founded
and sound, when compared to the prospects of the DARPA superman. The Elijah
Option challenges you. Whom do you serve?
http://www.veteransnewsnow.com/2014/09/30/nwo-overman-eupraxsophy-transhumanism/
Revelation 9
Humanity will undergo a radical transformation in the imminent future that will cause them to go to
WAR with God Almighty.
The quest for godhood started in the garden with Eve.
The Great Lie
“And the serpent said unto the woman, Ye shall not surely die: For God doth know that in the day ye eat thereof,
then your eyes shall be opened, and ye shall be as gods, knowing good and evil.” Gen. 3:4-5
The Great Apostasy
2 Thess. 2:3 Let no one deceive you in any way. For it will not be, unless the departure
the man of sin is revealed, the son of destruction,
comes first, and
Departure from the faith/Departure of the Holy Spirit and Bride from the Earth.
Manipulated duality paradigm of false light vs. dark
What is The Light?
“The elite have always (attempted to play) both sides of any political election, both sides of any internal revolution,
and both sides of any particular war… all done to perpetuate war forever. This is how they have historically
maintained power, by manipulating a false duality to manipulate our thoughts and emotions. The elite objective is
nearly always the same, getting the public to accept more control and give away even more freedom. Their first
World Order may be designed to take away our national borders and what’s left of our financial independence,
unveiling total surveillance. A second World Order may be needed to take away our very humanity, turning us all
into technologically mind-controlled robots. In between, more chaos will be required and created, some form of
controlled opposition will be needed. Problem-Reaction-Solution.
(http://deusnexus.wordpress.com/2014/07/14/the-giver/).”
Duality is being handed to all human beings on this planet as the only paradigm and giving us only a few solutions
to choose from – this is the Phoenix Rising or Order out of Chaos theory presented by Luciferians.
Christ taught us that He is the Way, the Truth, and the Light.
Lucifer pretends to have or a “anti” or contrasted view on the Way, the Truth, and the Light.
We are to chose between the two, but who is correct and why?
Is there really only two choices or just ONE!
The DUALITY PARADIGM
This is the lie fed to all humans who just glance at the notion of Truth:
"The belief that duality is an integral part of the ability to experience Wholeness
and thus an important component to establish a new paradigm of consciousness and health. In the current
paradigm of consciousness, duality is perceived to be a binary state of mutual exclusion. One sees this notion
reflected in human thought and
language where something must be “either X or Y”, but not “both X and Y”. A new paradigm of consciousness is
required that no longer operates in a “dualistic” notion of “either/or”, but one that conveys a “holistic” notion of
“both/and”. We currently view duality as a disjunctive rather than a conjunctive aspect of Being.
The difference between this dualistic and
holistic paradigm of consciousness can be symbolically expressed in the language of logic
(http://www.academia.edu/734932/Duality_Wholeness_and_a_New_Paradigm_of_Consciousness_and_Health)."
This is the Truth of Who we are and Who created us:
Isaiah 45:5 I am Yahweh, and there is none else; besides me there is no God. I will gird you, though you have not
known me; 6 that they may know from the rising of the sun, and from the west, that there is none besides me: I am
Yahweh, and there is no one else. 7 I form the light, and create darkness; I make peace, and create evil. I am
Yahweh, who does all these things. 8 Distil, you heavens, from above, and let the skies pour down righteousness: let
the earth open, that it may bring forth salvation, and let it cause righteousness to spring up together; I, Yahweh,
have created it. 9 Woe to him who strives with his Maker -- a potsherd among the potsherds of the earth! Shall the
clay ask him who fashions it, "What are you making?" or your work, "He has no hands?" 10 Woe to him who says
to a father, "What have you become the father of?" or to a woman, "With what do you travail?"
Matthew Henry's Concise Commentary
45:5-10 There is no God beside Jehovah. There is nothing done without him. He makes peace, put here for all good; and creates
evil, not the evil of sin, but the evil of punishment. He is the Author of all that is true, holy, good, or happy; and evil, error, and
misery, came into the world by his permission, through the wilful apostacy of his creatures, but are restrained and overruled to
his righteous purpose. This doctrine is applied, for the comfort of those that earnestly longed, yet quietly waited, for the
redemption of Israel. The redemption of sinners by the Son of God, and the pouring out the Spirit, to give success to the gospel, are
chiefly here intended. We must not expect salvation without righteousness; together the Lord hath created them. Let not
oppressors oppose God's designs for his people. Let not the poor oppressed murmur, as if God dealt unkindly with them. Men are
but earthen pots; they are broken potsherds, and are very much made so by mutual contentions. To contend with Him is as
senseless as for clay to find fault with the potter. Let us turn God's promises into prayers, beseeching him that salvation may
abound among us, and let us rest assured that the Judge of all the earth will do right.
Pulpit Commentary
Verse 7. - I form the light, and create darkness. It has been recently denied that there is any allusion in these words, or in those
which follow, to the Zoroastrian tenets; and it has even been asserted that the religion of the early Achaemenian kings was free
from the taint of dualism. But according to some authorities, "a god of lies" is mentioned in the Behistun inscription; and the
evidence is exceedingly strong that dualism was an essential part of the Zoroastrian religion long before the time of Cyrus (see
'Ancient Monarchies,' vol. 2. pp. 332, 333, 2nd edit.). It is quite reasonable to suppose that Isaiah would be acquainted with the
belief of the Persians and Medes, who had come in contact with the Assyrians as early as B.C.. 830; and a warning against the
chief error of their religion would be quite in place when he was holding up Cyrus to his countrymen as entitled to their respect
and veneration. The nexus of the words, "I am the Lord, and there is none else. I form the light, and create darkness," is such as
naturally to suggest an intended antagonism to the Zoroastrian system. Under that, Ormuzd created "light" and "peace," Ahriman
"darkness" and "evil." The two were eternal adversaries, engaged in an inter-ruinable contest. Ormuzd, it is true, claimed the
undivided allegiance of mankind, since he was their maker; but Ahriman was a great power, terribly formidable - perhaps a god
(diva) - certainly the chief of the devas. It was from Zoroastrianism that Manicheism derived its doctrine of the two principles,
and to the same source may, with much probability, be traced the "devil-worshippers" of the Zagros mountain chain.
John 14:6 Jesus said to him, "I am the way, the truth, and the life. No one comes to the Father,
but by me.”
Gen 2:17 But of the tree of the knowledge of good and
evil, thou shalt not eat of it: for in the day that thou
eatest thereof thou shalt surely die.
Life
Light and Dark
Good and Evil
Are not the
source.
God is the
Source.
Evil
Good
Satan is attempting to bring life out of Good and Evil.
Transhumanism
Transgenics
Transcendence
Singularity
Unity
All Religions
All Economies
All Nations
All Races
Gen 3:1 Now the serpent was more subtle than any animal of the field which Yahweh God had made. He said to the woman, "Yes,
has God said, 'You shall not eat of any tree of the garden?'" 2 The woman said to the serpent, "Of the fruit of the trees of the
garden we may eat, 3 but of the fruit of the tree which is in the midst of the garden, God has said, 'You shall not eat of it, neither
shall you touch it, lest you die.'" 4 The serpent said to the woman, "You won't surely die, 5 for God knows that in the day you eat it,
your eyes will be opened, and you will be like God, knowing good and evil." 6 When the woman saw that the tree was good for
food, and that it was a delight to the eyes, and that the tree was to be desired to make one wise, she took of the fruit of it, and ate;
and she gave some to her husband with her, and he ate. 7 Both of their eyes were opened, and they knew that they were naked.
They sewed fig leaves together, and made themselves aprons.
The Tree
Let us begin by describing the Tree, formally known as the Tree of Knowledge of Good and Evil. The word for
knowledge, da'at, is used later to describe the marital union between Adam and Eve. Therefore an alternative
translation might be: the Tree of Union Between Good and Evil.
And this is the crux of the matter: When God created the world, He clearly defined right from wrong. All moral
issues were objective and not subjective. There was one, obvious, absolute morality. True, one could choose to do
the wrong thing, but that choice was clear.
Yet God did create one place of moral confusion: the Tree. Eating from the Tree would actually internalize a
confusion between right and wrong. Avoiding this fate was Adam and Eve's one mitzvah to observe. And were they
to refrain from eating -- i.e. from entering that state of confusion -- the world would have reached its ultimate
completion. Mankind would have been immortal; forever in Paradise.
The Tree had a tremendous alluring power, primarily in how it affected the senses: Eve first listens to the snake's
seduction. She is then attracted to the look of the tree. She then takes the fruit in hand and tastes it. As the verses
say: "And when the woman saw that the tree was... a delight to the eyes... she took of the fruit, and did eat..."
(Genesis 3:6).
When Adam and Eve eat from the tree, it triggers a new modus operandi for the entire human experience: The
senses become more powerful than the intellect. And because all sensory delights are by nature subjective, at this
point man's frame of reference becomes personal rather than universal. Thus each person feels empowered to
decide for themselves between right and wrong, and moral confusion enters the world.
http://www.jewishpathways.com/chumash-themes/garden-eden
Consequences of Sin
To further appreciate this fusion of good and evil, let's look at the consequences of the sin:
1) Adam is told that the fields will produce not only grain, but also weeds. Originally, when you planted wheat, you got only
wheat.3 But when Adam chose to enter a state of confusion between right and wrong, God responded by fusing good and bad into
the very fabric of the natural world. Just as my choice to plant wheat produces a mixture of weeds, so too in the moral realm: I
may think I'm making the correct choice, but in fact I may be misled toward a path of moral corruption.
2) Eve is told that her children will be born and raised with pain. Why should this natural human activity require such anxiety
and effort? The reason is that before the sin, all human activities were value neutral. Just as breathing is essential for life and is
done naturally and without fanfare, so too all other bodily needs such as procreation and childbirth were done in the same
manner. Only when wisdom was confused with sensual desire, did our natural activities become more difficult. The process of
procreation is the most sensual of all human activities; therefore, this realm became mixed with physical and emotional trauma.
Attaining Wisdom
Adam and Eve were aware of what they were doing. They knew that that the Tree was off limits. As we said earlier, the
delineation between good and evil was quite clear. And it was not that they were lacking anything in the Garden of Eden. So what
did they feel was missing?
Adam and Eve lacked the opportunity to actualize their commitment to God by entering a state of challenge and then choosing
wisely. They felt that a world that did not allow them to overcome such confusion was a sign of insufficient commitment. So they
chose to enter this state willingly.
It is said that there are two ways to attain wisdom: either to learn about it intellectually, or to acquire it through life experience.
From a sensory perspective, the thrill of experience is surely unmatched. But at the same time, it is fraught with danger. Do we
really need to experience every drug and every decadent activity to know that it's not for us? For after all, we've all seen how the
result of these experiences can carry the danger of permanent physical or emotional scarring.
That is why God's discussion with Adam and Eve after the sin is not about punishment, but about consequence. God says: If this is
the choice you are making -- the path of challenge -- then this is how your life will play out. And as the progenitors of all
humanity, Adam and Eve's choices have (unfortunately) affected all their descendants, for all generations.
http://www.jewishpathways.com/chumash-themes/garden-eden
The Snake
A very enigmatic figure in this story is the snake. What kind of animal is this that speaks and tempts Adam and Eve? Actually, it is hard for
us to imagine the primordial snake, since part of the snake's punishment was a metamorphosis of what and who he is.
Before the sin of Adam and Eve, we find the snake described in detail in the Bible. He is depicted as "cunning," he speaks to Eve, he walks,
and he even seems to have his own volition and will. After the sin, he is punished in that he will now crawl on his stomach, his food will
be dirt, and there will eternal enmity between himself and man. What was the snake originally, and what did he do to deserve such a
downfall?
Most kabbalistic commentators equate the snake with the Yetzer Hara -- the self-destructive tendencies to move away from God.4 What is
the function of the Yetzer Hara? Why were such tendencies created? And why was a snake chosen to represent this?
The purpose of God's creating the world was to bestow goodness on mankind. The ultimate good is to not give someone a gift, but to
empower him to accomplish on his own. Imagine someone training for the Olympics with his coach serving in the role of the opponent. If
the coach does not oppose him with all his strength and wiles, the athlete will be upset with him. And when the student manages to
overcome the coach, the coach is happy at his own downfall -- since it is his role to finally be vanquished.
The Yetzer Hara is our coach. Any rational person would desire a worthy opponent to overcome. Therefore the original snake was almost
human, walking on legs, speaking intelligently, and able to present a world view alternate to God's. In that sense, the snake is the ultimate
servant of God and man. He is the force which gives us the ability to choose between two worldviews -- as long as the choice is balanced
and the snake is not too difficult to overcome.
When the choice was between intellectual and sensual, the snake needed to be able to tempt man with a sensual experience. However, he
needed to clothe it in the guise of the rational and objective truth. Therefore the snake was almost human in his abilities.
When man failed that test, the snake himself needed to undergo a metamorphosis. He needed to become the obstacle and temptation for a
different humanity, who now could be easily led astray. Therefore the intelligent rational snake becomes a dirt dwelling mute creature. All
his food tastes like earth. He is down in the dirt with no ability to lift himself up, and he cannot even communicate this since he lost his
speech. Why?
Originally, the fruits of the trees -- representing all levels of pleasure -- were accessible to man. There was nothing lacking, as long as the
"one command" was observed. Only after the sin could man think that pleasure was to be found outside the service of God. Thus, just as the
snake could not appreciate any pleasure without the dirt with it, so too man cannot appreciate the highest level of spiritual pleasure,
unless he has something physical along with it.
This is our opponent, which is appropriate for the world we live in, post-sin.
http://www.jewishpathways.com/chumash-themes/garden-eden
Naked and Bare
Adam and Eve started out "naked and unashamed" (Genesis 2:25), but after eating from the Tree of Knowledge, "they became aware of their
nakedness, and made themselves clothes" (Genesis 3:7).
Why the shift?
Before eating from the Tree, Adam and Eve saw each other first and foremost as souls. They knew the soul is the essence of a human being, with the
body serving merely as a protective covering. Since Adam and Eve were focused on the spiritual side, they weren't self-conscious about their bodies.
However, after eating from the Tree, human perception of the physical world changed. The physical senses enticed as if possessing a value of their
own. Adam and Eve's "eyes opened" to a focus on the body. The body had become a distraction from the soul and when this happened, Adam and Eve
were ashamed of their naked bodies. For a spiritual being, can there be any greater humiliation than to be sized up as something superficially
physical?
This explains why animals, who have no divine soul, never feel compelled to put on clothes. But for Adam and Eve, the body needed to be covered, in
order to de-emphasize the external, and to let the soul shine through.
Ashamed Before God
After Adam and Eve eat and realize the catastrophic change that they have caused in the world, they try to hide from God. God figuratively comes
looking for them, and calls out into the void of the world, "Adam, where are you?" Yet doesn't God know where they are? And do Adam and Eve
really think they can hide?
Adam and Eve are embarrassed by their nakedness, but this time it's not the physical lack of clothing. It is the shame to be in front of God. They have
failed in the one task given to them, and are now "naked," devoid of mitzvot.
Adam and Eve know that God has every right to deal with them harshly. But that is not God's approach. He offers them a chance to correct. If Adam
and Eve will willingly come to God and acknowledge their mistake, that itself can trigger a reversal of the damage done. This is the concept of
teshuva: acknowledging one's mistake, and undertaking not to do it again.5
God would like to give Adam and Eve a chance to own up to their actions. But instead, Adam blames Eve, and Eve blames the snake. And so, God
must implement the painful consequences, with the goal of correcting the defective behavior.
The story of the Tree of Knowledge is the ongoing story of humanity. We are convinced of the correctness of our actions. And when we err, God
presents another chance to realize and admit our mistake. If we do, we draw closer to God than ever before. But if we egotistically defend our
position, then we further carve an identity separate from God, putting us outside the true reality.
Even though at first Adam and Eve did not choose correctly, we still can. And in doing so, we can rectify that seminal sin, and bring about a return to
Eden, the utopian era for which we all so desperately yearn.6
http://www.jewishpathways.com/chumash-themes/garden-eden
1 - You shall have no other gods before Me.
Yahweh’s Commandments
2 - You shall not make idols.
3 - You shall not take the name of the LORD your God in vain.
4 - Remember the Sabbath day, to keep it holy.
5 - Honor your father and your mother.
6 - You shall not murder.
7 - You shall not commit adultery.
8 - You shall not steal.
9 - You shall not bear false witness against your neighbor.
10 - You shall not covet.
Satan’s Commandments
http://www.jimsearcy.com/GAStones.htm
Christ is the Tree of Life
Jesus the Bread of Life
John 6:25 When they found him on the other side of the lake, they asked him, "Rabbi,18 when did you get here?" 26 Jesus answered, "I tell you the
truth, you are looking for me,19 not because you saw miraculous signs20 but because you ate the loaves and had your fill. 27 Do not work for food
that spoils, but for food that endures21 to eternal life,22 which the Son of Man23 will give you. On him God the Father has placed his seal24 of
approval." 28 Then they asked him, "What must we do to do the works God requires?" 29 Jesus answered, "The work of God is this: to believe25 in the
one he has sent."26 30 So they asked him, "What miraculous sign27 then will you give that we may see it and believe you?28 What will you do? 31
Our forefathers ate the manna29 in the desert; as it is written: 'He gave them bread from heaven to eat.'c "30 32 Jesus said to them, "I tell you the truth,
it is not Moses who has given you the bread from heaven, but it is my Father who gives you the true bread from heaven. 33 For the bread of God is
he who comes down from heaven31 and gives life to the world." 34 "Sir," they said, "from now on give us this bread."32 35 Then Jesus declared, "I am33
the bread of life.34 He who comes to me will never go hungry, and he who believes35 in me will never be thirsty.36 36 But as I told you, you have seen
me and still you do not believe. 37 All that the Father gives me37 will come to me, and whoever comes to me I will never drive away. 38 For I have
come down from heaven38 not to do my will but to do the will39 of him who sent me.40 39 And this is the will of him who sent me, that I shall lose
none of all that he has given me,41 but raise them up at the last day.42 40 For my Father's will is that everyone who looks to the Son43 and believes in
him shall have eternal life,44 and I will raise him up at the last day." 41 At this the Jews began to grumble about him because he said, "I am the bread
that came down from heaven." 42 They said, "Is this not Jesus, the son of Joseph,45 whose father and mother we know?46 How can he now say, 'I
came down from heaven'?"47 43 "Stop grumbling among yourselves," Jesus answered. 44 "No one can come to me unless the Father who sent me
draws him,48 and I will raise him up at the last day. 45 It is written in the Prophets: 'They will all be taught by God.'d49 Everyone who listens to the
Father and learns from him comes to me. 46 No one has seen the Father except the one who is from God;50 only he has seen the Father. 47 I tell you
the truth, he who believes has everlasting life.51 48 I am the bread of life.52 49 Your forefathers ate the manna in the desert, yet they died.53 50 But
here is the bread that comes down from heaven,54 which a man may eat and not die. 51 I am the living bread55 that came down from heaven.56 If
anyone eats of this bread, he will live forever. This bread is my flesh, which I will give for the life of the world." 57 52 Then the Jews58 began to argue
sharply among themselves,59 "How can this man give us his flesh to eat?" 53 Jesus said to them, "I tell you the truth, unless you eat the flesh 60 of the
Son of Man61 and drink his blood,62 you have no life in you. 54 Whoever eats my flesh and drinks my blood has eternal life, and I will raise him up
at the last day.63 55 For my flesh is real food and my blood is real drink. 56 Whoever eats my flesh and drinks my blood remains in me, and I in
him.64 57 Just as the living Father sent me65 and I live because of the Father, so the one who feeds on me will live because of me. 58 This is the bread
that came down from heaven. Your forefathers ate manna and died, but he who feeds on this bread will live forever." 66 59 He said this while
teaching in the synagogue in Capernaum.
18. John 6:25 - S Mt 23:7
19. John 6:26 - ver 24
20. John 6:26 - ver 30; S Jn 2:11
21. John 6:27 - Isa 55:2
22. John 6:27 - ver 54; S Mt 25:46; Jn 4:14
23. John 6:27 - S Mt 8:20
24. John 6:27 - Ro 4:11; 1Co 9:2; 2Co 1:22; Eph
1:13; 4:30; 2Ti 2:19; Rev 7:3
25. John 6:29 - 1Jn 3:23
26. John 6:29 - S Jn 3:17
27. John 6:30 - S Jn 2:11
28. John 6:30 - S Mt 12:38
29. John 6:31 - Nu 11:7-9
30. John 6:31 - Ex 16:4,15; Ne 9:15; Ps 78:24; 105:40
31. John 6:33 - ver 50; Jn 3:13,31
32. John 6:34 - Jn 4:15
33. John 6:35 - Ex 3:14; Jn 8:12; 10:7,11; 11:25;
14:6; 15:1
34. John 6:35 - ver 48,51
35. John 6:35 - S Jn 3:15
36. John 6:35 - Jn 4:14
37. John 6:37 - ver 39; Jn 17:2,6,9,24
38. John 6:38 - Jn 3:13,31
39. John 6:38 - S Mt 26:39
40. John 6:38 - S Jn 3:17; Jn 4:34; 5:30
41. John 6:39 - Isa 27:3; Jer 23:4; Jn 10:28; 17:12; 18:9
42. John 6:39 - ver 40,44,54
43. John 6:40 - Jn 12:45
44. John 6:40 - S Mt 25:46; Jn 3:15,16
45. John 6:42 - Lk 4:22
46. John 6:42 - Jn 7:27,28
47. John 6:42 - ver 38,62
48. John 6:44 - ver 65; Jer 31:3; Jn 12:32
49. John 6:45 - Isa 54:13; Jer 31:33,34; 1Co 2:13; 1Th 4:9; Heb
8:10,11; 10:16; 1Jn 2:27
50. John 6:46 - S Jn 1:18; 5:37; 7:29
51. John 6:47 - S Mt 25:46
52. John 6:48 - ver 35,51
53. John 6:49 - ver 31,58
54. John 6:50 - ver 33
55. John 6:51 - ver 35,48
56. John 6:51 - ver 41,58
57. John 6:51 - Heb 10:10
58. John 6:52 - S Jn 1:19
59. John 6:52 - Jn 7:43; 9:16; 10:19
60. John 6:53 - Mt 26:26
61. John 6:53 - S Mt 8:20
62. John 6:53 - Mt 26:28
63. John 6:54 - ver 39
64. John 6:56 - Jn 15:4-7; 1Jn 2:24; 3:24; 4:15
65. John 6:57 - S Jn 3:17
66. John 6:58 - ver 49-51; Jn 3:36; 5:24
http://www.biblestudytools.com/john/6.html
Genospirituality:
genetic engineering for spiritual and
religious enhancement.
http://www.ncbi.nlm.nih.gov/pubmed/18782654
The One World Religion
When The False Prophet brings all religions together in the world. The main convergence of many peoples will be
based on the cure for their “duality” (the lower and higher self) and unharmonious lives. A simple device, Mark of
the Beast, will be offered at first then will become mandatory. This device will be multifold in its operation.
Psiometrics, Harmonic Resolution, Neurotechnology, hydrosonic fluid technology (turns body water into a
speaker), etc…. Combine this with “Google glass” and all ones neuronal activity will be subject to the control of the
Luciferians. You will think, act, and have your being in Satan.
The idea is that they are trying to “cure” the animal self and the spiritual self into one by bringing them into
“harmonious resonance” together. These idolaters have no idea what sin is and why we have fallen from grace and
must have the Son of God, Jesus Christ living inside of us to have salvation. It is imperative that we undergo
“transformation” by the Holy Spirit, who convicts one of their sins. This conviction turns the soul away from
seeking fleshly desires by a godly repentance. By taking the Mark of the Beast, they are in fact, dissolving ANY
conviction from the Holy Spirit, even to the point that one will no longer hear His voice.
True Transformation comes from Yahweh in heaven. When you KNOW that you have caused Him hurt because
you transgressed His laws, you know you are doomed and separated from God. The only way to eternal salvation is
through the redemptive blood of Jesus Christ. Transgression of God’s laws is death. Christ is the only one who was
capable of shedding His pure blood to redeem us from death.
In the next slide you can see how the Luciferians have reduced the mind and how it works to produce perfect and
positive results every time. Literally, this is the science of how to become your own god! Please be careful with the
heretical nature of these lies. You cannot become god! This same lie was acted upon in the Garden of Eden by Eve
and look where this took mankind. Into death and utter separation from God forever. The only way to God and to
become a child of God is through Jesus Christ, the Son of God.
http://www.harmonicresolution.com/Human%20Alembic%20Graphic.htm
Combining the Genome, Vironome, and the “Chip” will bring about the Mark of the Beast
Characterization of the 80170NX (ETANN) chip sigmoidal transfer function for a device Vgain=3.3V
J. Calvin ; Steven K. Rogers ; Daniel R. Zahirniak ; Dennis W. Ruck ; Mark E. Oxley
[+] Author Affiliations
Proc. SPIE 1965, Applications of Artificial Neural Networks IV, 654 (September 2, 1993); doi:10.1117/12.152567
Text Size: A A A
From Conference Volume 1965
Applications of Artificial Neural Networks IV
Steven K. Rogers
Orlando, FL | April 11, 1993
Abstract
abstract
This paper presents results from experiments on determining the sigmoidal transfer function in Intel's Electronically Trainable Analog Neural
Network (ETANN), the 80170NX chip. Accurate simulator training off-chip is needed in order to reduce training time and to minimize chip-in-loop
training (on-chip), which if done in excess, can decrease the chip's useful life. For this reason accurate characterization of the ETANN chip is of
significant importance to application designers for off-chip simulation. A series of tests were performed to collect data from eight ETANN chips for
analysis. After computing an average response value from eight chips and performing a minimum mean-square-error search for a gain coefficient
(also called a hardness parameter in the sigmoidal function), a transfer function and gain coefficient were found. Using this transfer function and
gain coefficient in a custom neural network simulator, called Neural Graphics, a performance evaluation was accomplished. A test shows a direct
correlation between the Neural Graphics simulator output and the ETANN chip's output using the same synaptic weights and the test data.
Moreover, for this test we have found that Neural Graphics, while using the characterized transfer function from this research, performed in a
superior manner to that of iNNTS simulators. For researchers who desire to interface their own custom simulator with the ETANN hardware, a
similar procedure as developed in this paper should be followed.
© (1993) COPYRIGHT SPIE--The International Society for Optical Engineering. Downloading of the abstract is permitted for personal use only.
Topics
Computer hardware ; Interfaces ; Neural networks ; Simulations ; Visualization
Citation
J. Calvin ; Steven K. Rogers ; Daniel R. Zahirniak ; Dennis W. Ruck and Mark E. Oxley
"Characterization of the 80170NX (ETANN) chip sigmoidal transfer function for a device Vgain=3.3V", Proc. SPIE 1965, Applications of Artificial
Neural Networks IV, 654 (September 2, 1993); doi:10.1117/12.152567; http://dx.doi.org/10.1117/12.152567
-Rudolf Steiner: Fall of the Spirits of Darkness Lecture 13
"A longing will arise (and become) general opinion: Whatever is spiritual, whatever is of the spirit, is nonsense, is
madness! endeavors to achieve this will be made by bringing out remedies to be administered by inoculation just as
inoculations have been developed as a protection against diseases, only these inoculations will influence the human
body in a way that will make it refuse to give a home to the spiritual inclinations of the soul. People will be
inoculated against the inclination to entertain spiritual ideas. Endeavors in this direction will be made; inoculations
will be tested that already in childhood will make people lose any urge for spiritual life."
[page 199, 200] Steiner:
"I have told you that the spirits of darkness are going to inspire their human hosts, in whom they will be dwelling,
to find a vaccine that will drive all inclination towards spirituality out of people's souls when they are very young,
and this will happen in a roundabout way through the living body. Today, bodies are vaccinate against one thing
and another; in future, children will be vaccinated with a substance which it will certainly be possible to produce,
and this will make them immune, so that they do not develop foolish inclinations connected with spiritual life
'foolish' here, of course, in the eyes of materialists."
Some people will want E.T.’s to save them.
Some are anticipating a return of their Messiah.
Some are anticipating the Messiah.
Some are looking for A.I. to save them.
Some are looking to leave the Earth entirely and colonize another planet.
Some believe that those who are ready will transcend to a different plane of existence.
All will get as they desire.
For all of them are deceived.
2 Thess. 2:8Then that lawless one will be revealed whom the Lord will slay with the
breath of His mouth and bring to an end by the appearance of His coming; 9that is,
the one whose coming is in accord with the activity of Satan, with all power and signs
and false wonders, 10and with all the deception of wickedness for those who perish,
because they did not receive the love of the truth so as to be saved.…
There are indeed two paths to choose from, but please
educate yourself as to which path leads where.
PUBLIC RELEASE DATE:
13-Aug-2014
Contact: Mary Beth O'Leary
moleary@cell.com
Researchers uncover how Ebola virus disables immune response
The Ebola outbreak in West Africa has brought a lot of attention to the deadly virus. According to the World Health Organization, up to 90% of
those infected with Ebola die from the virus. Now, researchers publishing August 13 in the Cell Press journal Cell Host & Microbe reveal how Ebola
blocks and disables the body's natural immune response. Understanding how Ebola disarms immune defenses will be crucial in the development of
new treatments for the disease.
Dr. Gaya Amarasinghe and colleagues from Washington University School of Medicine along with collaborators from the Icahn School of Medicine
at Mount Sinai and UT Southwestern Medical Center at Dallas show how the Ebola protein VP24 disrupts the cell's innate immune response, a
crucial early step on the virus's path to causing deadly disease.
"We've known for a long time that infection with Ebola obstructs an important immune compound called interferon," said Amarasinghe. "Now we
know how Ebola does this, and that can guide the development of new treatments."
According to the researchers, VP24 works by preventing the transcription factor STAT1, which carries interferon's antiviral message, from entering
the nucleus and initiating an immune response. As part of a rapid immune response, the cell allows STAT1 an "emergency access lane" to the
nucleus. Rather than block all nuclear transfer, however, VP24 focuses on blocking STAT1's "emergency access lane."
"Normally interferon causes STAT1 to enter the cell nucleus, where it activates the genes for hundreds of proteins involved in antiviral responses,"
Dr. Daisy Leung from Washington University School of Medicine said. "But when VP24 is attached to STAT1, it can't get into the nucleus."
"One of the key reasons that Ebola virus is so deadly is because it disrupts the body's immune response to the infection," said Dr. Chris Basler of the
Icahn School of Medicine at Mount Sinai. "Figuring out how VP24 promotes this disruption will suggest new ways to defeat the virus."
These findings come at a critical time for Ebola research. If researchers carry out further study of VP24, it can open the door to new possibilities for
disarming the protein's effect on immune response.
###
Cell Host & Microbe, Xu et al.: "Ebola Virus VP24 Targets a Unique NLS Binding Site on Karyopherin Alpha 5 to Selectively Compete with Nuclear
Import of Phosphorylated STAT1."
http://www.eurekalert.org/pub_releases/2014-08/cp-ruh081114.php
They are PREPARING the population for the Mark of the BEAST!
Wearable's WILL BECOME injections!!!!!
Wearable Early Warning for Chem-Bio Threats
The Defense Threat Reduction Agency (DTRA) is interested in proposals for wearable sensor technologies to
provide an early warning capability for chemical and biological threat exposure.
The ideal deployable system would be a very low burden, minimally invasive, wear-and-forget device. An
emphasis is given to multi-parameter sensing system designs capable of differentiating typical battlefield stresses
from measureable responses to chemical and biological threat exposure, to include physiological responses.
- See more at: http://globalbiodefense.com/2014/11/12/wearable-early-warning-chem-biothreats/#sthash.FHXSif4H.dpuf
“Vaccinating susceptible
populations during the initial stage of a pandemic is critical
to containment,”Dr. Alan Magill, DARPA program manager, says in an official statement. “We’re looking at
plant-based solutions to vaccine production as a more rapid and efficient alternative to the standard egg-based
technologies, and the research is very promising.” (DARPA’s Blue Angel – Pentagon Prepares Millions of Vaccines
Against Future Global Flu, RT, July 28, 2012) http://www.globalresearch.ca/is-the-u-s-military-manufacturingebola-vaccines-to-be-tested-on-its-soldiers-to-advance-us-ability-to-wage-war/5402847
SEE ALSO:
http://www.occupycorporatism.com/researchers-develop-new-pain-free-ways-to-make-sure-you-are-vaccinated/
“DoD and the commercial diagnostics industry has made considerable progress toward better, cheaper, more
applicable, Clinical Laboratory Improvement Amendments (CLIA) -waived diagnostic tools,” states the
announcement. “However, more work is needed to provide the warfighter with advanced warning on when to
deploy these tools. Ideally, personnel should not have to wait for overt symptoms to develop before engaging
diagnostics.”
Proposals must specify the measured markers and the anticipated exposure/performance parameters indicated by
the planned measurements.
Sensor systems should include all required components, including batteries appropriate for an extended mission
lifetime, and should not require reagents or other consumables.
The effort is part of DTRA Broad Agency Announcement: HDTRA1-14-CHEM-BIO-BAA. The deadline to submit
questions is Dec. 3. Initial proposals are due by Dec. 22, 2014.
- See more at: http://globalbiodefense.com/2014/11/12/wearable-early-warning-chem-biothreats/#sthash.FHXSif4H.dpuf
A battery made up of billions of nanoscale batteries
November 11, 2014 –
http://www.kurzweilai.net/a-battery-made-up-of-billions-of-nanoscale-batteries
Researchers at the University of Maryland (UMD) have invented, using a structure based on a nanopore: a tiny hole
in a ceramic sheet that holds electrolyte to carry the electrical charge between nanotube electrodes at either end.
The researchers note in a paper in Nature Nanotechnology that such a design would provide the maximum power
and energy from a given battery chemistry because the internal resistances for ion transfer and the volume of
electrochemically inactive components would be minimized. That means smaller, more powerful batteries that
operate longer without a recharge —- that is, significantly higher energy density and power density.
NOTICE!!! The solicitation numbers are the same!
http://globalbiodefense.com/2014/11/12/wearable-early-warningchem-bio-threats/
https://www.fbo.gov/index?s=opportunity&mode=form&id=7e80ca2fd06
01a1b397a6f6856c8514e&tab=core&_cview=1
DARPA is expanding globally.
Through public or private means, the world is trying to tackle the Ebola crisis head on. However, the Defense
Advanced
Projects Research Agency wants to be able to prevent the next Ebola crisis from ever
getting off the ground.
“We keep seeing these unexpected biothreats pop up along the globe, and we don’t want to be in the position where we are
reactive,” said Alicia Jackson, deputy director of DARPA’s Biological Technologies Office. “We want to be in a position where we’re
building a platform technology that can be applied not just to Ebola, but the next thing.”
In order to facilitate that, DARPA’s Biological Technologies Office announced a new simplified funding vehicle that aims to help
inject money into an array of bioscience areas. Known as the EZ BAA, this new model whittles down the process for biotech
companies, startups or academics to get involved with DARPA’s newest office.
Jackson said the need for this type of funding became clear after she spent time talking to various people in the biosciences
community who had no idea DARPA could be a source for funding or a way to see their technology come to life.
“One of the things that it drove me to understand was that if we were going to be able to reach these new technical communities
of interest, especially the small startups who don’t have the infrastructure to do a rigorous type of federal contracting, we need to
create a different mechanism to engage folks,” Jackson said.
The EZ BAA differs from the agency’s standard broad agency announcement in that it’s not concentrated on achieving a specific
technological capability, but it’s open to any transformative biotech idea. A proposal submitted under this new plan only has to be
a two-page white paper, as opposed to a 40-to-60-page project summary that is normally required under a traditional BAA.
The idea is reminiscent of the RFP-EZ, which was introduced last year as a way to attract companies who have never done
business with the government to engage in the contracting process. Any project that DARPA picks up will receive up to $700,000
in “seedling” funding, with the BTO office holding the projects to “very clear milestones.”
- See more at: http://fedscoop.com/darpa-ez-baa/#sthash.qnIYXBEb.dpuf
Government contracting for small business made EZ
By Kathryn Sadasivan · Wednesday, May 15, 2013 · 1:14 pm
A request for proposals pilot project, developed under the White House Presidential Innovation Fellows program, is
starting to gain ground in the small business IT community.
RFP-EZ launched with the posting of five website development and database contract offerings, four of which were
also announced through FedBizOps, the standard government RFP process. Contract bids received through RFP-EZ
were on average 30 percent lower than FedBizOps.
As a testament to RFP-EZ’s ability to draw a wider pool of businesses into the world of federal contracting, during
the pilot period alone, 270 firms that had never done business with government before have come forward to take
advantage of the new platform.
RFP-EZ is a win-win for small technology companies and the federal government, according to federal CTO Todd
Park. Through the online program, small technology firms get easier access to the government’s nearly $77 billion
IT supply chain while federal government agencies get the support and innovation they need to do more with less.
The pilot program is particularly beneficial to companies lacking experience or administrative support generally
required for the standard government RFP process. Through RFP-EZ, small technology firms can learn about and
compete for important IT contracts on a simplified and more easily accessible platform.
Developed jointly by the Small Business Administration and the White House Presidential Innovation Fellows
program, the team used private and public sector insights to create an online platform that opened up the
government market place to a larger variety of companies, saving taxpayer money in the process. The fellows also
prioritized transparency by publishing RFP-EZ’s code openly on GitHub during the development process.
-See more at: http://fedscoop.com/rfp-ez-shows-signs-of-impacting-small-business-itbids/#sthash.CBRSKUr9.dpuf
-Small tech companies are being CONSUMED by DARPA and GOOGLE!!!!
The new Anti-Viral
Drugs
DRACO ("Double-stranded RNA (dsRNA) Activated Caspase Oligomerizer") is a group of experimental antiviral
drugs under development at the Massachusetts Institute of Technology. DRACO is reported to have broadspectrum efficacy against many infectious viruses, including Marburg marburgvirus and Zaire ebolavirus, dengue
flavivirus, Amapari and Tacaribe arenavirus, Guama bunyavirus, H1N1 influenza and rhinovirus. DRACO is
reported to induce rapid apoptosis selectively in virus-infected mammalian cells, while leaving uninfected cells
unharmed.[1][2]
As of January 2014, work has moved to Draper Laboratory for further testing and development; "the team looks
forward to larger scale animal trials and clinical human trials within a decade or less".[3] Rider presented at the
SENS Foundation's SENS6 conference.[4]
DRACO is selective for virus-infected cells. Differentiation between infected and healthy cells is made primarily via
the length and type of RNA transcription helices present within the cell. Most viruses produce long dsRNA helices
during transcription and replication. In contrast, uninfected mammalian cells generally produce dsRNA helices of
fewer than 24 base pairs during transcription. Cell death is effected via one of the last steps in the apoptosis
pathway in which complexes containing intracellular apoptosis signaling molecules simultaneously bind multiple
procaspases. The procaspases transactivate via cleavage, activate additional caspases in the cascade, and cleave a
variety of cellular proteins, thereby killing the cell.[1]
Rider TH, Zook CE, Boettcher TL, Wick ST, Pancoast JS, Zusman BD (2011). "Broad-spectrum antiviral
therapeutics". PLoS ONE 6 (7): e22572. doi:10.1371/journal.pone.0022572. PMC 3144912. PMID 21818340.
Fiona Macrae (11 August 2011), "Greatest discovery since penicillin: A cure for everything - from colds to HIV",
The Daily Mail (UK) "Todd Rider Joins Draper to Continue Antiviral Therapeutics Development" (Press release).
Cambridge, MA. PRWeb. January 8, 2014. Retrieved April 8, 2014. "PANACEA broad-spectrum antiviral
therapeutics". SENS6 Proceedings. Retrieved 2014-04-11. Parise, Tim (2013). "L'Affaire Famille". The Maui
Company. p. 271. Retrieved 2014-04-29.
http://en.wikipedia.org/wiki/DRACO_%28antiviral%29
When viruses infect a cell, they take over its
cellular machinery for their own purpose — that
is, creating more copies of the virus. During this
process, the viruses create long strings of doublestranded RNA (dsRNA), which is not found in
human or other animal cells. As part of their
natural defenses against viral infection, human
cells have proteins that latch onto dsRNA, setting
off a cascade of reactions that prevents the virus
from replicating itself. However, many viruses
can outsmart that system by blocking one of the
steps further down the cascade.
Rider had the idea to combine a dsRNA-binding
protein with another protein that induces cells to
undergo apoptosis (programmed cell suicide) —
launched, for example, when a cell determines it
is en route to becoming cancerous. Therefore,
when one end of the DRACO binds to dsRNA, it
signals the other end of the DRACO to initiate cell
suicide.
Read more:
http://www.33rdsquare.com/2013/09/anti-viraldrugs-may-soon-beavailable.html#ixzz3LQ6QA99l
In Figure 1, influenza viruses bind to specific carbohydrate
structures on the surface of airway cells to gain entry. In
Figure 2, nanotrap particles effectively mimic the cell
surface so that their carbohydrate structures "trap" viruses
and prevent infection.
DRACO is a chimera made up of two kinds of proteins: APAF1 and PKR. PKR recognizes double stranded
RNA and APAF1 activates the cell's apoptosis pathway. Double stranded RNAs (dsRNA) are unique to
only virus infected cells and is absent in normal cells. In other words, when DRACO recognises the same
dsRNA two or three times, APAF1 is activated leading to immediate cell death. Viruses usually
manipulate proteins early in the apoptotic pathway and not the later ones. This super-protein works
because it does not target the virus itself but it signals an infected cell to commit suicide.
http://www.plosone.org/article/fetchObject.action?uri=info%3Adoi%2F10.1371%2Fjournal.pone.0022572&representation=PDF
One man wants to end viral infections once and for all... by making them
commit suicide.
Let’s find out a little bit more about the maker of DRACOs.
Over a decade ago, Dr. Todd Rider was in the shower when he had just that idea. Last July, he and
his colleagues published the early results of their work; the article’s simple title, "Broad-Spectrum
Antiviral Therapeutics," belies the potential breakthrough, which is nothing less than a completely
new approach. Rather than containment (antivirals) or prevention (vaccines), this method
actually kills virus-infected cells, without harming normal cells. It’s an offensive weapon in the
battle against viruses: dubbed Double-stranded RNA (dsRNA) Activated Caspase Oligomerizer
(DRACO), it eliminated 15 pathogens, from the common cold to H1N1 influenza to hemorrhagic
fevers like the dengue virus. It works across 11 cell types, including human heart, lung, kidney,
and liver cells. Mice infected with lethal doses of influenza were completely cured by DRACO
treatment.
In other words, as Rider puts it, "DRACO has the potential to revolutionize the treatment and
prevention of viral illnesses, just as antibiotics revolutionized the treatment and prevention of
bacterial infections in the mid-twentieth century."
What if there were a way to kill all viruses dead?
If anyone’s qualified to advance the war on viruses, it’s Todd Rider. He grew up with what he calls
"role models of scientists and inventors doing high-risk, high-return, multidisciplinary research
in science fiction stories" — that’d be the science-adventurers classic to Jules Verne and H. G.
Wells, Dr. Rudy Wells in The Six Million Dollar Man, and, less happily, Dr. Bruce Banner, of The
Incredible Hulk. He still peppers his conversations with references to experimental mice that
might "turn big and green and angry" or become super-intelligent as in Flowers for Algernon.
That early vision of science as exciting and adventurous stuck with him, and he wishes today’s
would-be scientists had similar role models.
As a youngster he built a robot dog from scratch, studied ways to transport water around the
world as hydrogen instead of whole water, and devised a rocket staging system that could carry
50 percent more payload into orbit with no extra fuel, compared to existing launch vehicles. He
filed a patent for the system when he was 17.
http://www.theverge.com/2012/4/11/2940938/todd-rider-draco-doomsday-device-virus
The same year, 1986, he enrolled at MIT. His eclectic interests took him in several directions at once, but what he really wanted
was to merge two disciplines, biology and engineering. "Everyone in the biology department thought I was crazy to be interested
in engineering," he says, "and likewise everyone in the engineering department thought I was crazy to be interested in biology."
(Now, he points out, we have this discipline called bioengineering.) Courses at the Harvard Medical School supplemented his
biology training, and when he graduated in 1995 he had four degrees, capped by a PhD in electrical engineering and computer
science.
With his ranging curiosity, he found the job market dishearteningly uninteresting. "I was really quite dismayed to see that most of
the recruiters on campus were from the financial industry, and indeed they still are," he says. The best and brightest among his
peers, as he saw it, went off to devise market simulations rather than pursue research and development. He signed on with a small
biotech startup called Aeiveos. Based in Seattle, the company had Silicon Valley in its DNA: started by Robert Bradbury, a software
developer and early Oracle employee, its investors included Bradbury’s old boss, Oracle chairman Larry Ellison. Aeiveos —
derived from the Greek "aei" ("forever") and "veos" ("young") — planned deep research into the aging process. Bradbury had long
sought a "cure" for old age; he likened the human genome to Windows NT in its complexity, and believed that within 20 years
science would crack the genetic code, leading to radically enhanced lifespans if not immortality. (A longtime futurist and SETI
advocate, he also conceptualized the Matrioshka Brain — a computer large enough to harness the power of a star.)
The plan was ambitious, just the thing that’d appeal to a fan of The Six Million Dollar Man. Rider was hired as a senior scientist,
but within two years the company’s funding withered away. Cast again into an unappealing job market, Rider met with a
recruiter from the MIT Lincoln Laboratory, the university’s long-standing national defense R&D institution.
"When they made the job offer, I kept trying to find out exactly what the job would be, and they'd just say nebulously, 'Oh, we
work on whatever the Air Force wants us to work on,’" Rider says. "It was really the only job offer I had, and I needed to eat, so I
showed up." He started out working on missile defense, but soon realized he could dovetail his biotechnology interests with the
lab’s larger goals. The lab wanted sensors with military applications. "So, I thought, ok, I'll develop a sensor for military
applications that uses bioengineering."
That project became CANARY, a sensor that uses jellyfish genes to detect pathogens. "My philosophy was to borrow from nature
wherever possible," says Rider, by using one of the most well-known, ubiquitous pathogen detectors: white blood cells. These
workhorses of the human immune system recognize microbial invaders within seconds. By modifying them with genes from the
Aequorea victoria jellyfish, which produces green fluorescent protein (GFP), Rider had an effective biosensor. In the presence of a
pathogen, the white blood cells would glow, thanks to the GFP.
http://www.theverge.com/2012/4/11/2940938/todd-rider-draco-doomsday-device-virus
CANARY quickly went from lab project to commercial technology, while Rider moved on to his next challenge. By
early 2000 he’d begun to think about antivirals. The progression made sense: CANARY could identify pathogens
and bacteria, treatable with antibiotics. But it also identified pathogenic viruses, for which there often were no
treatments. That meant "you could simply tell people what they were going to die of." A better option had to exist.
The genesis for DRACO went like this: "It just occurred to me one day in the shower: oh, well, let's cross-wire these
two to connect the successful detection of the long double-strand RNA with the successful final activation of
suicide in the infected cells." Translated, Rider’s plan involved two parts. First, he knew that certain proteins could
detect double-strand RNA, or dsRNA. The "D" in DRACO, dsRNA is found in almost all viruses (a strain of
hantavirus is among those that don't), but not in healthy cells — it’s a near-perfect marker. But viruses shut down
most responses to dsRNA; likewise, they disable another natural pathway inside cells, one that causes apoptosis, or
cell death. Rider thought if he could combine the two, he’d have a viable method, one that detected dsRNAcontaining cells and then caused them to commit cellular suicide.
“DRACO has been funded by grant AI057159 from the National Institute of Allergy and Infectious Diseases and the
New England Regional Center of Excellence for Biodefense and Emerging Infectious Diseases, with other funding
coming from DARPA, the Defense Threat Reduction Agency, and the office of the Director of Defense Research and
Engineering (http://www.draper.com/emailedAnnouncements.html#nanotech_influenza . “
As of January 2014 DARPA has been funding
DRACO and with defense-funded Lincoln
Laboratories.
http://www.theverge.com/2012/4/11/2940938/todd-rider-draco-doomsday-device-virus
“Dr. Rider: There are two broad mechanisms in the body. One which people are more familiar with is the immune
system, consisting of a relatively small number of white blood cells running around your body producing
antibodies and doing other things to look for specific pathogens that you have previously had or been vaccinated
for. The other which people are less familiar with is that every cell in your body has natural defenses built inside of
it. Think of it as a burglar alarm inside every house. DRACO works by rewiring certain parts of that burglar alarm
to make them more effective (http://www.wtxl.com/sports/draco-keeps-the-bad-guys-away/article_038f739a478f-50e8-ad05-2858ba6a6638.html .”
Could DRACO and FunVax be used together to “rewire” certain undesirable pieces in our brains?
My research on FunVax - http://www.youtube.com/watch?v=XTdxFwi8L4g -- Mark of the Beast, Anti-Soul
Vaccinations, and Your Salvation.
FunVax (Fundamental vaccine) is a Department of Defense project started in 2004. It’s purpose, originally, was to
illiminate terrorists in the Middle East. The method genetically causes a “fanatic” to give up their religious beliefs
by attacking the gene VMAT2 (http://www.genecards.org/cgi-bin/carddisp.pl?gene=SLC18A2 ,
http://en.wikipedia.org/wiki/Vesicular_monoamine_transporter_2 ). This gene eventually became known as the
God Gene. The God Gene predisposes people to have spiritual experiences. Department of Defense scientists used
this information to create a vaccine against religious fundamentalism. It was a viral vaccine that spreads via air
and is designed to inhibit the expression of the VMAT2 gene causing people to become less religious.
“just because we can explain the neurobiological and genetic basis of religious
experience, this does not mean that there is no God
(http://threes.com/index.php?option=com_content&view=article&id=2206:the-god-gene&catid=81:religion&Itemid=61 ).”
The following is an interview with Whistle Blower Joey Lambardi. It was recorded over the phone at 1:32 pm April 23rd, 2011 and transcribed by
volunteers at the FunVax blog.
(FunVax blog) What is your background?
(Joey Lambardi) Well, I grew up in New York. Always was into film, ever since I was a little kid. I lived in the same Neighborhood as Martin Scorsese,
so I think that had a big influence on me – being Italian American and being into film. I can point out the house that Scorsese grew up in. Christmas
Eve one year, I remember sitting in the living room with my mom and step dad and their friends watching Good Fellas. I begged my parents from
that point on for a camcorder. I didn’t get one until my birthday two years later. There is something about film and Italians, I don’t know what it is,
but we go together like cheese and honey. So, yeah, I started making these little videos with a Hi-8 camera and editing them on my parents VHS
machine. Then things just progressed. When I graduated High School, I wasn’t interested in college or anything. So, I joined the military. I didn’t
know they did video stuff in the military, but after talking with a recruiter I learned that they do. So I signed up for a unit called Combat Camera.
And I did that for six years, well about six years, a little shy of six years. That changed, you know, when I got leaked this information about FunVax.
(FB) And how exactly did that happen, how did you get that information?
(JL) I was on this assignment that seemed really bizarre. It just didn’t make any sense, you know? I was told that I was to document a war hero’s
return home from Iraq. That was it – simple right? But the normal chain of command was altered. In this case, the first time in six years, I was to
report to a CIA named agent Fleming as well as Army Col. Harris who from what I gather was a big wig intel guy at the pentagon. So, that was
weird, especially for such a boring sounding assignment. It got weirder when I was mailed a package that contained a DVD and a stack of
documents. There were a lot of things blacked out, but it was all stuff related to FunVax. The package was address to me, it was sent to the house
where I where I was, you know, videotaping, the family that I was documenting.
(FB) Can you tell us about the videos?
(JL) Sure. There were two videos actually. One looked like a homemade amateur video that was of a party in a common area, like a lunch room or
something. There’s a cake that says “FunVax is a Go” on it and there was a sign that said Congratulations FunVax. But that was all the funvax related
information. It was just a normal party, the people were talking about normal things. The second video was a lot more informative. It was DoD
footage from a lecture hall in the pentagon. The video was date stamped 4/13/05 so someone was holding onto this for awhile. I received it, the
second week of February of this year. So, on it, it had one of the guys from the other video, the party video, giving a presentation. I just have an 8
minute clip from this presentation, but basically, this guy, he must be a scientist. This guy is giving a lecture about the brain and a gene called
VMAT2 to a group of men in suits as well as various military uniforms. He talks about religion and was showing MRI brain scans. He said that the
inhibition of VMAT2 could, over time, cause a persons brain to shift from a religious brain structure, they scientifically, you know they call it
phenotype…but basically, you can change a religious brain to a non-religious brain structure. VMAT2 is apparently the scientific name for what
people term the God Gene. At the end of the clip he says that he filed a proposal under the name FunVax to begin experimenting with the VMAT2
gene with the goal of creating a virus, like the flu virus, that will remove or replace this gene from people in the Middle East. Their goal of course
was to create peace in the Middle East.
The goal of FunVax or whatever new concoction they will come out with to “cure” people of the God Gene is to
physically change their Phenotype.
By changing the Phenotype of a person, they are in essence changing the appearance or expression of that
individual, which they appear to be an entirely “new person”. “A phenotype (from Greek phainein, meaning "to
show", and typos, meaning "type") is the composite of an organism's observable characteristics or traits, such as its
morphology, development, biochemical or physiological properties, phenology, behavior, and products of behavior
(such as a bird's nest). Identical twins share the same genotype, since their genomes are identical; but they never
have the same phenotype, although their phenotypes may be very similar. This is apparent in the fact that their
mothers and close friends can always tell them apart, even though others might not be able to see the subtle
differences. Further, identical twins can be distinguished by their fingerprints, which are never completely
identical.(http://en.wikipedia.org/wiki/Phenotype ).”
Fundamental Vaccine may NOT be fake!
Vmat2 and Cytosine.
Cytosine (C) is one of the four main bases found in DNA and RNA, along with adenine, thymine and guanine. It is a
pyrimidine derivative, with a heterocyclic aromatic ring and two substituents attached (an amine group at position
4 and a keto group at position 2). The nucleoside of cytosine is cytidine. In Watson-Crick base pairing, it forms
three hydrogen bonds with guanine (http://www.princeton.edu/~achaney/tmve/wiki100k/docs/Cytosine.html).
http://web.pdx.edu/~tothm/religion/Is%20God%20in%20Our%20Genes.pdf
Hamer identifies various genes that might be candidates for the genetic aspect of self-transcendence. After a few
failed attempts (there are, after all, approximately 35,000 genes present in the human genome), Hamer explains
how he and his research team hit upon the VMAT2 gene sequence. The VMAT2 gene sequence is polymorphic and
has three alleles. What Hamer found was that one allele (the A33050C polymorphism) is strongly associated with
those who report high levels of self-transcendence. The VMAT2 gene sequence is responsible for coding for
proteins that make up a group of neurotransmitters known as monoamines, which leads to the next piece of the
puzzle: What is the brain mechanism by which the God gene generates spiritual, self-transcendent experiences?
(http://threes.com/index.php?option=com_content&view=article&id=2206:the-godgene&catid=81:religion&Itemid=61).”
Brain Mechanism
“Monoamines are a group of neurotransmitters (including serotonin and dopamine) responsible for (or implicated
in) a number of neuro-chemical phenomena, including the feeling of euphoria, positive emotion, and the
propensity for addiction. Roughly speaking, monoamines are responsible for the "high" feelings we experience
when we have ingested various controlled substances, stimulants, or psychoactive plants. What is important is that
monoamines are the biochemical mediators for the interplay between experience and emotion (between the
limbic-brain system and the thalamo-cortical brain system). In short, monoamines play a significant role in
ineffable feelings of "self-transcendence" that Hamer's questionnaire measures. (Could this be a reason why Marajuana
is now legal in the State of Colorado and quickly to spread across America?)
(Parenthetically, Hamer also discusses the compelling results found by Andrew Newberg and his colleagues
regarding the connection between meditation, spiritual experience, and the discovery that key parts of the brain
undergo what is called "deafferentiation" or a relative decrease in neural activity. Newberg's book, Why God Won't
God Away, is equally readable and worth exploring for those who wish to examine the neuro-chemical basis of
religious belief. Unlike Hamer, Newberg does not attempt to identify any genetic contribution to the human
propensity to experience self-transcendence.) http://threes.com/index.php?option=com_content&view=article&id=2206:the-godgene&catid=81:religion&Itemid=61.”
The Buddhist theory is not the subject under scrutiny here. I have studied to some depth the religious views of
Buddhism, Hinduism, etc… and found their lack of understanding of the Triune God ineffectual to achieving
salvation through the death and resurrection of Jesus Christ. In pointing out the distinction below, I believe it’s
highly important to show the “twins” experiment. This is indicative of the testing of the phenotype and genotype of
gene expression.
http://web.pdx.edu/~tothm/religion/Is%20God%20in%20Our%20Genes.pdf
Without VMAT2…
http://www.ncbi.nlm.nih.gov/pubmed/23410751
The VMAT2 or FunVax could not destroy the “God Gene” from our brains, nor could it suppress the function
entirely since it has been proven to have fatal results in mice. IF, “if”, this FunVax has been unleashed in the Middle
East upon unsuspecting Arabs, could this be why the N.W.O. Luciferians are now using the “Arab Springs” and the
dissolving of sovereign nations worldwide to fully accomplish their desires to bring the Son of Perdition to light
and suppress all mankind to their will by enforcing the Mark of the Beast?
Could it be that Satan, in his never ending attempt to show himself as God, be trying to reproduce the effect of the
Holy Spirit? I’ve often wondered how Satan would truly express a functioning trinity so that many will be deceived
by him and call him god when, in fact, he is still merely just an imposter and created being trying desperately to be
like Yahweh.
Still the fact remains that Satan has been attempting to show humanity that he is god since the Garden of Eden and
even no is in the greatest position he has had yet to prove to mankind that he can make mankind immortal. Once
he can achieve this, and I believe Yahweh will allow this to happen as part of the Strong Delusion, Satan will be
given 7 years to accomplish his goals and thus the greatest trial that humanity has ever faced will be
catastrophically endured till Christ’s return to the Mount of Olives.
This could possibly preclude that phenotypes are desired for a “FunVax” and not changing our
genes specifically.
http://web.pdx.edu/~tothm/religion/Is%20God%20in%20Our%20Genes.pdf
Even though all this research into the God Gene is fun and intriguing, one thing we should always keep in mind.
Satan is very good at beguiling the most sincere individual. Duality is but one trick that the Devil and demon both
use to cause humanity to stumble before an Almighty God in heaven.
There is only ONE TRUTH.
ONE PRINCIPLE in motion that defines all knowledge, wisdom and all that contains “beingness”.
This understanding only resides in One, the Creator of Heaven and Earth, unto which it has been given unto to
mankind to seek out and to know the One True God, Yahweh.
Proverbs 25:2 - It is the glory of God to conceal a thing, but the glory of kings is to search out a matter.
http://biblehub.com/proverbs/25-2.htm - Matthew Henry's Concise Commentary
Prov. 25:1-3 God needs not search into any thing; nothing can be hid from him. But it is the honour of rulers to
search out matters, to bring to light hidden works of darkness. 4,5. For a prince to suppress vice, and reform his
people, is the best way to support his government. 6,7. Religion teaches us humility and self-denial. He who has
seen the glory of the Lord in Christ Jesus, will feel his own unworthiness. 8-10. To be hasty in beginning strife, will
bring into difficulties. War must at length end, and might better be prevented. It is so in private quarrels; do all
thou canst to settle the matter. 11,12. A word of counsel, or reproof, rightly spoken, is especially beautiful, as fine
fruit becomes still more beautiful in silver baskets. 13. See what ought to be the aim of him that is trusted with any
business; to be faithful. A faithful minister, Christ's messenger, should be thus acceptable to us. 14. He who
pretends to have received or given that which he never had, is like the morning cloud, that disappoints those who
look for rain. 15. Be patient to bear a present hurt. Be mild to speak without passion; for persuasive language is the
most effectual to prevail over the hardened mind. 16. God has given us leave to use grateful things, but we are
cautioned against excess.
Ecclesiastes 3:11
The Excellence in God's Works
…10 I have seen the task which God has given the sons of men with which to occupy themselves. 11 He has made
everything appropriate in its time. He has also set eternity in their heart, yet so that man will not find out the work
which God has done from the beginning even to the end. 12 I know that there is nothing better for them than to
rejoice and to do good in one's lifetime;…
Cross References
Romans 11:33
Oh, the depth of the riches of the wisdom and knowledge of God! How unsearchable his judgments, and his paths beyond tracing out!
Genesis 1:31
God saw all that he had made, and it was very good. And there was evening, and there was morning--the sixth day.
Job 5:9
He performs wonders that cannot be fathomed, miracles that cannot be counted.
Proverbs 16:4
The LORD works out everything to its proper end-- even the wicked for a day of disaster.
Ecclesiastes 1:13
I applied my mind to study and to explore by wisdom all that is done under the heavens. What a heavy burden God has laid on mankind!
Ecclesiastes 7:13
Consider what God has done: Who can straighten what he has made crooked?
Ecclesiastes 7:23
All this I tested by wisdom and I said, "I am determined to be wise"-- but this was beyond me.
Ecclesiastes 8:17
then I saw all that God has done. No one can comprehend what goes on under the sun. Despite all their efforts to search it out, no one can discover
its meaning. Even if the wise claim they know, they cannot really comprehend it.
Ecclesiastes 11:5
As you do not know the path of the wind, or how the body is formed in a mother's womb, so you cannot understand the work of God, the Maker of
all things.
http://biblehub.com/ecclesiastes/3-11.htm
Winston Churchill
Winston Churchill Truth is
incontrovertible.
Malice may attack it
and ignorance may
deride it, but, in the
end, there it is.
Those who take the Mark of the Beast will be :
Revelation 13:17 ESV
So that no one can buy or sell unless he has the mark, that is, the name of the beast or the number of its name.
Revelation 16:2 ESV
So the first angel went and poured out his bowl on the earth, and harmful and painful sores came upon the people who bore the
mark of the beast and worshiped its image.
Revelation 14:9-11 ESV
And another angel, a third, followed them, saying with a loud voice, “If anyone worships the beast and its image and receives a
mark on his forehead or on his hand, he also will drink the wine of God's wrath, poured full strength into the cup of his anger, and
he will be tormented with fire and sulfur in the presence of the holy angels and in the presence of the Lamb. And the smoke of
their torment goes up forever and ever, and they have no rest, day or night, these worshipers of the beast and its image, and
whoever receives the mark of its name.”
Revelation 13:16-18 ESV
Also it causes all, both small and great, both rich and poor, both free and slave, to be marked on the right hand or the forehead, so
that no one can buy or sell unless he has the mark, that is, the name of the beast or the number of its name. This calls for wisdom:
let the one who has understanding calculate the number of the beast, for it is the number of a man, and his number is 666.
Those who take the Mark, maybe immortal and will burn forever in the Lake of fire.
Revelation 14:11 ESV
And the smoke of their torment goes up forever and ever, and they have no rest, day or night, these worshipers of the beast and its
image, and whoever receives the mark of its name.”
"And in those days shall men seek death, and shall not find it; and shall desire to die, and death shall flee from them." Revelation
9:6
Changing a Human beings Phenotype can have disastrous consequences. If the Mark of the Beast were to be
distributed in a vaccine form, the resulting change in phenotype expression could be compared to, “Toxoplasma
gondii is a parasitic protozoan whose effects on human behavior, personality and other phenotypic traits have been
studied most thoroughly, often in the context of the manipulation theory, the theory suggesting that many parasites
change the phenotype of their host to increase their chances of transmission to a new host by, for example,
predation. There are various reasons why this particular protozoon has become a favored model for evolutionary
parasitologists, biologists and also psychiatrists…. Toxoplasma is an excellent model for studying the manipulation
hypothesis as it is trophically transmitted from an intermediate to a definitive host by predation. In contrast to
behavioral patterns induced by directly or, more commonly, sexually transmitted parasites, the behavioral patterns
induced by a trophically transmitted parasite are relatively easy to recognize (Parker et al., 2009). For example, in a
sexually transmitted parasite, the parasite’s and the host’s genes have similar interests: they both ‘try’ to program
the host to increase the probability of host reproduction. (http://jeb.biologists.org/content/216/1/127.full).”
Toxoplasma gondii is a single example of how a parasite infects its host and changes the phenotype to ensure its
own survival. The Mark of the Beast would not even have to be predatory like a parasite, but could be transferred
through something as simple as peer pressure, societal acceptance, or sexual intercourse (See The Emerging Risks
of Live Virus…).
If the Mark of the Beast is “chimeric” in its construction, then, it could thrive in bodily fluids and could also
replicate via sexual intercourse as does Ebola (“Men who have recovered from the illness can still spread the virus
to their partner through their semen for up to 7 weeks after recovery. For this reason, it is important for men to
avoid sexual intercourse for at least 7 weeks after recovery… ” http://www.who.int/csr/disease/ebola/faq-ebola/en/.
See also - “…coming into direct contact with semen, vaginal fluids, saliva or even sweat could still be risky while a
patient is symptomatic http://www.scientificamerican.com/article/let-s-talk-about-ebola-survivors-and-sex/ .”)
upon 90 days after infection.
The Emerging Risks of Live Virus
&
Virus Vectored Vaccines:
Vaccine Strain Virus Infection,
Shedding & Transmission
http://www.nvic.org/CMSTemplates/NVIC/pdf/Live-Virus-Vaccines-and-Vaccine-Shedding.pdf
http://www.nvic.org/CMSTemplates/NVIC/pdf/Live-Virus-Vaccines-and-Vaccine-Shedding.pdf
http://www.nvic.org/CMSTemplates/NVIC/pdf/Live-Virus-Vaccines-and-Vaccine-Shedding.pdf
One of the goals that seems to be actively in the works in our present age is to genetically bioidentify all the human
family. My original thought was that National Geographic and the Luciferians were doing this to find out which
“families” every human being belonged to by collecting genetic samples from every human on the Earth and
thereby create a “holocaust 2.0” where they will round everyone up (i.e. Noah – Shem, Ham, or Japheth), but I was
wrong. Well, partly wrong. I still believe they will do this to know who is who in the world one day.
I was a fool to believe that they would round up over 5.5 billion people. This is as insane a quest as it is to rid the
whole world of the annoying gnat.
A greater goal is being sought by the Luciferians.
To find and map the complete Human Virome.
By mapping the Human Virome, all virus, their rate of adaptation, and all the information contained therein will
help the Luciferians to exterminate select people groups by release of plagues upon the whole world. Whole
strains of select people groups could be wiped out within weeks if not months. We are talking millions upon
millions of people wiped out just like the Spanish Flu in 1918 and even worse.
Zech. 14:12Now this will be the plague with which the LORD will strike all the peoples who have gone to war against Jerusalem;
their flesh will rot while they stand on their feet, and their eyes will rot in their sockets, and their tongue will rot in their mouth.
13It will come about in that day that a great panic from the LORD will fall on them; and they will seize one another's hand, and
the hand of one will be lifted against the hand of another.…
Revelation 15-16 discuss the Last Plagues unleashed upon mankind.
Rev. 6:7 When the Lamb opened the fourth seal, I heard the voice of the fourth living creature say, "Come!" 8 I looked, and there
before me was a pale horse! Its rider was named Death, and Hades was following close behind him. They were given power over
a fourth of the earth to kill by sword, famine and plague, and by the wild beasts of the earth.
The LIE is that there is a race war.
The Truth is that there will be a race
extermination of all undesirables.
This is Eugenics on Steroids.
“An individual's exposure to viruses is influenced by their geographic location, age, lifestyle, and even the season of the year, while their
susceptibility to disease is affected by preexisting immunity and both viral and human genetics. Characterizing all human viruses will require
casting a very wide nest and analyzing samples collected around the globe from a diverse collection of patients exhibiting a wide range of
unexplained symptoms as well as carefully epidemiologically matched healthy subjects. Blood, respiratory secretions, feces, urine, skin swabs, and
tissues may all be used for viral metagenomics (Figure 1). Samples likely to yield the most “new” human viruses will likely be from children and
immunocompromised patients whose viral loads are expected to be higher and last longer. Subjects living in crowded locations with poor sanitation,
nutrition, and healthcare standards are also expected to generally carry a higher viral burden. Sick travelers, exposed to viruses to which they have
no preexisting immunity, may also be rich sources of “new” viruses. When will the human virome be completed? When, despite geographically
diverse and intense sampling of heavily exposed and susceptible populations, the rate of “new” human virus discovery falls to near zero, the human
virome (at least as it exists at that time) may be considered near completion. The ongoing exchange of viruses between host species will require
ongoing surveillance for zoonotic outbreaks of emerging viral pathogens (http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3573120/).”
http://www.nvic.org/CMSTemplates/NVIC/pdf/Live-Virus-Vaccines-and-Vaccine-Shedding.pdf
http://www.plospathogens.org/article/info%3Adoi%2F10.1371%2Fjournal.ppat.1003146
http://www.nvic.org/CMSTemplates/NVIC/pdf/Live-Virus-Vaccines-and-Vaccine-Shedding.pdf
“GeoVax is developing two Ebola vaccines, GOVX-E301 and
GOVX-E302. Both are recombinant MVA (modified vaccinia
Ankara) vaccines designed to produce non-infectious viruslike particles (VLPs) displaying the Ebola virus glycoprotein.
GOVX-E301 is being developed as a single-dose vaccine for
epidemic response against the ZEBOV strain of Ebola, the
virus responsible for the current outbreak. GOVX-E302 is
being developed for routine immunization and is designed to
protect against all three versions of Ebola known to be lethal
in humans. GOVX-E302 is anticipated to be used in a twodose regimen…. With the knowledge gained from our
experience in developing HIV vaccines, we believe our MVAvectored Ebola vaccines have the unique attributes required
for success and will offer superior results over other Ebola
vaccines in development. We are therefore fast tracking this
program with the objective of having an ‘epidemic-ready’
GOVX-E301 vaccine available by 2016.”
“Our Ebola vaccine program is a natural extension of our
MVA vaccine delivery platform,” Dr. McNally continued. “It
is a complementary asset to our lead HIV vaccine program, to
which we remain committed. We continue to be actively
engaged in discussions with the HIV Vaccine Trials Network
(HVTN) and the National Institutes of Allergy and Infectious
Disease (NIAID) regarding the design of our next clinical
study and various trial designs are being considered.”
(http://www.geovax.com/newsevents/entry/2014/10/02/geovax-announces-initiation-ofebola-vaccine-development-program.html).”
http://www.nvic.org/CMSTemplates/NVIC/pdf/Live-Virus-Vaccines-and-Vaccine-Shedding.pdf
It is important to lay down the specifics here because, contemplating the Mark of the Beast that could be given as a
vaccine is a HUGE implication of future impact on humanity as a whole. Just imagine, Aliens (fallen angels
disguised as our space brothers) come to Earth, have the “cure all” for every disease on the planet, and a vaccine is
administered to all willing human subjects. A vaccine would be PERFECT to distribute the Mark of the Beast
because if one’s lover or spouse were to not accept the vaccine, all one would have to do is have sexual intercourse
with the other and the live viral vector would be distributed into the unknowing individual via bodily fluids (semen
or pituito-serous matter) and therefore would initially contain the “Mark”. Some distinctions need to be addressed
here. The significant “other” would be taking the Mark unknowingly and therefore not subject to the willful
submission and worship thereof of the Beast and his image, BUT with the contagion present in the body its
veritable replication would start changing the “information” in the body and thus the resulting goal would be
complete submission to the instructions laid out in the information received from the vaccine or dsRNA.
http://www.nvic.org/CMSTemplates/NVIC/pdf/Live-Virus-Vaccines-and-Vaccine-Shedding.pdf
The Holy Bible tells us:
Revelation 14:9 NIV
A third angel followed them and said in a loud voice: "If anyone worships the beast and his image and receives his
mark on the forehead or on the hand,
The word Beast can be translated in a few ways (this is just for sake of clarity).
http://www.blbclassic.org/lang/lexicon/lexicon.cfm?Strongs=G2342&t=KJV
http://www.blbclassic.org/lang/lexicon/Lexicon.cfm?strongs=G2226
http://dictionary.reference.com/browse/zoon
Zoon is often the Greek word used as Zoological or Zootic
Or better yet
http://www.merriam-webster.com/dictionary/-zoon
Spermatozoon is “plural spermatozoa; from Ancient Greek: σπέρμα "seed" and Ancient Greek: ζῷον "living being")
is a motile sperm cell, or moving form of the haploid cell that is the male gamete
(http://en.wikipedia.org/wiki/Spermatozoon ).”
The male seed is the progenitor of the “original sin.” If the Luciferians are using the male seed or the “original sin”
DNA or RNA
Adam did not sin in maliciousness, but
benevolence towards his wife, Eve. But Adam
still transgressed the commandments of God by
making Eve his first choice rather than
choosing God first, which is transgression
against the first commandment.
Will the Mark of the Beast
Come as a Virus, a Vaccine,
or a DNA altering
recombinant gene?
Let’s begin to make some connections.
What do VMAT2, DRACO, EBOLA, Stockpiling Ebola Survivor’s blood, and
FunVax all have in common?
&
http://whsc.emory.edu/home/publications/healthsciences/update/2014/july/hsu-july-2014.html
Not only is Emory university working on the VMAT2 “God gene”, but they are now on
the “payroll” of the 100’s of millions of dollar being given away by the Federal
government for the Brain Health Initiative.
http://www.braininitiative.nih.gov/index.htm
If you’ll remember, Emory University was the first
hospital to receive an infected Ebola patient in USA.
http://whsc.emory.edu/home/publications/health-sciences/update/2014/july/hsu-july-2014.html
There is so much more to delve into here and I pray that I will be able to do
a part 2 to this presentation and clear up some of the holes left in some
of these slides. There is so much information out there and our time to
expose the deeper truths of the lies that have enveloped our lives from
birth to our awakening, whichever comes first, is quickly passing.
The Lord will return.
Soon.
To make right all the pains and afflictions of the human race,
But,
We must be patient in our waiting for Him.
MARANATHA
My brothers and sisters.
Work Cited
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http://www.naturalnews.com/z036756_depopulation_agenda_eugenics_survivor.html
http://www.naturalnews.com/045318_fake_vaccines_DNA_harvesting_White_House.html
http://www.naturalnews.com/047089_Ebola_pandemic_government_lies_disinformation.html
http://www.naturalnews.com/046290_Ebola_patent_vaccines_profit_motive.html
http://www.prnewswire.com/news-releases/global-genetic-testing-industry-282285561.html
http://www.forbes.com/sites/davidkroll/2014/08/05/ebola-secret-serum-small-biopharma-the-army-and-big-tobacco/
http://globalbiodefense.com/
http://www.engadget.com/2014/11/08/darpa-expandny-prosthetics-ebola/
http://fedscoop.com/darpa-ez-baa/
http://www.ibtimes.com/ebola-virus-drug-developed-funding-same-us-defense-department-group-behind-internet-1651766
http://www.genengnews.com/gen-news-highlights/ebolawatch-darpa-offers-researchers-ez-money/81250573/
http://www.globalresearch.ca/is-the-u-s-military-manufacturing-ebola-vaccines-to-be-tested-on-its-soldiers-to-advance-us-ability-to-wage-war/5402847
http://www.bloomberg.com/news/2014-08-06/ebola-drug-from-tobacco-part-of-promising-therapies.html
http://time.com/3457472/see-how-ebola-drugs-grow-in-tobacco-leaves/
http://mashable.com/2014/08/17/ebola-serum-zmapp/
globalbiodefense.com/2014/11/12/wearable-early-warning-chem-bio-threats/
https://www.fbo.gov/index?s=opportunity&mode=form&id=492773dadadb498b4829a45c7a3e7073&tab=core&_cview=0
http://www.kurzweilai.net/a-battery-made-up-of-billions-of-nanoscale-batteries
http://fedscoop.com/rfp-ez-shows-signs-of-impacting-small-business-it-bids/
http://globalbiodefense.com/2014/11/09/darpa-bto-ez-baa-biotech-innovation/
http://www.pharmaceutical-technology.com/features/featureblue-angel-darpas-vaccine-manufacturing-challenge-4171658/
http://www.globalresearch.ca/darpa-s-blue-angel-pentagon-prepares-millions-of-vaccines-against-future-global-flu/32141
http://www.gulf-times.com/Mobile/Opinion/189/details/410783/Plant-based-vaccines-challenge-big-pharma-for-$3bn-flu-market
http://www.occupycorporatism.com/researchers-develop-new-pain-free-ways-to-make-sure-you-are-vaccinated/
http://www.pharmainfo.net/reviews/edible-vaccinesa-novel-approach
http://en.wikipedia.org/wiki/ZMapp
http://www.naturalnews.com/045418_flu_shots_influenza_vaccines_mercury.html
http://sharonkgilbert.com/?p=2627
http://en.wikipedia.org/wiki/Monoclonal_antibody
http://en.wikipedia.org/wiki/Fusion_protein
http://www.nytimes.com/2014/11/08/business/genetically-modified-potato-from-simplot-approved-by-usda.html?_r=1
http://www.bloomberg.com/news/2014-08-06/ebola-drug-from-tobacco-part-of-promising-therapies.html
http://stm.sciencemag.org/content/5/199/199ra113.full.pdf?keytype=ref&siteid=scitransmed&ijkey=0sAYN4XJB0f5s
http://mashable.com/2014/08/17/ebola-serum-zmapp/
http://en.wikipedia.org/wiki/Starch
http://jid.oxfordjournals.org/content/196/Supplement_2/S347.short
http://help.iedb.org/entries/50012939-Analysis-of-Ebola-virus-envelope-glycoprotein-GP-Prediction-of-HLA-class-II-restricted-T-cell-epitop
http://currents.plos.org/outbreaks/article/obk-14-0050-conservancy-of-mab-epitopes-in-ebolavirus-glycoproteins-of-previous-and-2014-outbreaks/
http://nprcresearch.org/news/ebola.php
http://news2.onlinenigeria.com/entertainment/369296-giveafricazmapp-or-africancure-challenging-nigeria-to-develop-zmapp-ebola-cure.html
http://www.ncbi.nlm.nih.gov/pubmed/10603327 - delta-peptide
http://www.freerepublic.com/focus/chat/3191066/posts?page=2378
http://jvi.asm.org/content/77/10/5902.short
http://www.whitehouse.gov/the-press-office/2014/07/31/executive-order-revised-list-quarantinable-communicable-diseases
http://www.cff.org/AboutCF/
http://www.acs.org/content/acs/en/noteworthy-chemistry/2014-archive/october-27.html
http://www.slideshare.net/uniquelee/airborne-ebola-blood-red-moon-and-comets
http://www.phe.gov/about/barda/Documents/barda-strategic-plan.pdf
http://health.utah.gov/epi/diseases/ebola/plan.pdf
http://www.rightdiagnosis.com/c/cf/misdiag.htm
http://cpj.sagepub.com/content/26/2/78.short
http://stm.sciencemag.org/content/5/199/199ra113
http://www.datamonitor.com/store/News/cystic_fibrosis_hiv_and_ebola_could_be_a_cure?productid=352F3774-FF2F-4898-924E-A41C052853B7
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC136726/
http://www.ncbi.nlm.nih.gov/pubmed/10482652/ - Mutational analysis of the putative fusion domain of Ebola virus glycoprotein.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC136726/ - Covalent Modifications of the Ebola Virus Glycoprotein
http://en.wikipedia.org/wiki/%CE%94F508
http://jscreen.org/learn-more/diseases/cystic-fibrosis/
http://www.slideshare.net/amepivax/epi-vax-ebolaanalysis-18august2014630pm
http://viralzone.expasy.org/all_by_protein/23.html
http://currents.plos.org/outbreaks/article/obk-14-0050-conservancy-of-mab-epitopes-in-ebolavirus-glycoproteins-of-previous-and-2014-outbreaks/
http://help.iedb.org/entries/50012939-Analysis-of-Ebola-virus-envelope-glycoprotein-GP-Prediction-of-HLA-class-II-restricted-T-cell-epitop
http://jvi.asm.org/content/77/10/5902.short - Lentivirus Vectors Pseudotyped with Filoviral Envelope Glycoproteins Transduce Airway Epithelia from the Apical Surface Independently of
Folate Receptor Alpha
http://www.globalresearch.ca/top-doctors-ebola-may-become-airborne-and-may-already-be-transmissible-via-aerosols/5405907
http://www.telegraph.co.uk/news/worldnews/ebola/11135883/Ebola-could-become-airborne-United-Nations-warns-of-nightmare-scenario-as-virus-spreads-to-the-US.html
https://leonclifforddotcom.files.wordpress.com/2014/08/chan-speech-1.jpg
https://leonclifforddotcom.files.wordpress.com/2014/08/chan-speech-2.jpg
https://leonclifforddotcom.files.wordpress.com/2014/08/chan-speech-3.jpg
https://leonclifforddotcom.files.wordpress.com/2014/08/who-speech.jpg
http://www.nature.com/srep/2012/121115/srep00811/full/srep00811.html
http://www.pharmaceutical-technology.com/features/featureblue-angel-darpas-vaccine-manufacturing-challenge-4171658/
http://www.globalresearch.ca/is-the-u-s-military-manufacturing-ebola-vaccines-to-be-tested-on-its-soldiers-to-advance-us-ability-to-wage-war/5402847
http://www.rh-negativenetwork.com/cloning-rh-negative-blood
http://www.datamonitor.com/store/News/cystic_fibrosis_hiv_and_ebola_could_be_a_cure?productid=352F3774-FF2F-4898-924E-A41C052853B7
http://www.technologyreview.com/news/532266/google-wants-to-store-your-genome/
http://www.thecommonsenseshow.com/2014/11/15/depopulation-could-a-speech-from-8-years-ago-hold-the-key-to-the-rapid-spread-of-ebola/
http://conservative-daily.com/2014/11/11/un-to-enforce-gun-control-with-obamas-help/
http://www.nationaljournal.com/defense/the-cyborg-medicine-of-tomorrow-is-inside-the-veteran-of-today-20141110
http://www.kurzweilai.net/ibm-developing-150-petaflops-supercomputers-for-national-labs
http://www.echoesofenoch.org/nephilimhybrids.conjob.htm
http://heavenawaits.wordpress.com/human-hybrids-can-they-be-saved/
http://paradoxbrown.com/modernhybridsnephilim.htm/
http://www.nephilimhybrids.com/ - These guys contort scripture way out of context - beware!
http://www.zerohedge.com/news/2014-11-16/what-difference-week-makes-international-diplomacy
http://global0biodefense.com/2014/11/13/nanoviricides-usamriid-crada-ebola-drug-bsl4/
http://sitchiniswrong.com/nephilim/nephilim.htm
http://abcnews.go.com/Health/ebola-america-timeline/story?id=26159719
http://time.com/3583724/meet-americas-top-ebola-doctor/?xid=newsletter-brief
http://time.com/3525869/cdc-changes-ebola-guidelines/
http://time.com/3522984/ebola-nigeria-who/
http://www.ibtimes.com/ebola-liberia-nation-backs-claim-us-authorized-dispatch-ebola-drug-infected-doctors-1655752
http://www.nytimes.com/interactive/2014/07/31/world/africa/ebola-virus-outbreak-qa.html?_r=0
http://en.wikipedia.org/wiki/Ebola_virus_epidemic_in_West_Africa
http://www.sciencemag.org/content/345/6202/1369
http://www.who.int/mediacentre/factsheets/fs103/en/
http://www.cdc.gov/vhf/ebola/outbreaks/history/chronology.html
http://www.sciencemag.org/content/early/2014/08/27/science.1259657.full.pdf?explicitversion=true
http://beast.bio.ed.ac.uk/tutorials
http://divinecosmos.com/start-here/davids-blog/1074-olympicsilluminati
http://www.bcrevolution.ca/secret_societies.htm
http://www.theforbiddenknowledge.com/hardtruth/secretsocietyindex.htm
https://www.facebook.com/notes/indigo-merovingian/the-octopus-bunge-and-the-luciferian-trust-chemical-lobotomy-of-the-holy-grail-b/184120071633325?fref=nf
http://illuminatusobservor.blogspot.com/2008/11/hydra-as-representation-of-osirian.html#axzz3JRVvvBCX
http://www.jimsearcy.com/GAStones.htm
http://deusnexus.wordpress.com/2014/04/06/captain-america-illuminati-game/
http://lifehopeandtruth.com/bible/10-commandments/the-ten-commandments/10-commandments-list/
http://www.jimsearcy.com/GAStones.htm
http://www.foxsports.com/nfl/story/simpsons-predicted-broncos-seahawks-super-bowl-over-eight-years-ago-013114
http://pinballking.blogspot.com/2010/07/whats-wrong-with-beatles-alot.html
http://www.theforbiddenknowledge.com/hardtruth/secretsocietyindex.htm
http://tolweb.org/tree/
http://www.jewishpathways.com/chumash-themes/garden-eden
http://www.gotquestions.org/does-God-use-evil.html
http://biblehub.com/isaiah/45-7.htm
http://beast.bio.ed.ac.uk/
http://www.snopes.com/politics/medical/ebolapatent.asp
http://marketdailynews.com/2014/08/05/all-americans-will-have-to-take-an-ebola-vaccine/
http://fas.org/sgp/crs/misc/RS21414.pdf
http://www.thedailybeast.com/articles/2014/11/22/meet-the-rescue-pilots-of-ebola-air.html
http://www.informationclearinghouse.info/article40012.htm
http://www.informationclearinghouse.info/article40013.htm
http://www.lewrockwell.com/2014/10/no_author/its-the-worse-strain-of-ebola-ever/
http://clinicaltrials.gov/show/NCT02041715
http://clinicaltrials.gov/ct2/show/NCT02267109?term=ebola&rank=2
https://vaccinecentral.wordpress.com/2010/05/11/are-vaccines-mandatory/
http://www.nvic.org/nvic-vaccine-news/february-2014/2014-state-vaccine-legislation-in-america---battle.aspx
http://www.livingwhole.org/god-does-not-support-vaccines/
http://www.theorganicprepper.ca/heres-why-wont-be-lining-up-for-the-ebola-vaccine-08062014
http://www.vaclib.org/news/religion.htm
http://laissez-faire.ch/en/articles/transhumanism-the-next-step-of-civilization/
http://alltencommandments.com/all/new/vaccinations.php
http://www.know-vaccines.org/?page_id=247
http://www.youtube.com/channel/UC4z1W8oHYn_9EaUdE-hBIag
http://www.biblestudytools.com/john/6.html
http://www.astro.umd.edu/~miller/teaching/astr380f09/slides27.pdf
http://sciencefocus.com/feature/space/our-future-space
http://globalwarming-arclein.blogspot.com/2011/10/longevity-research-speeding-up.html
http://globalwarming-arclein.blogspot.com/2011/11/alien-human-genetic-blending-with-lloyd.html
http://www.lloydpye.com/interventiontheory.htm
http://www.sott.net/article/271770-Study-shows-men-wont-be-losing-their-Y-chromosome-anytime-soon
http://gloryinthetruth.blogspot.com/2014_02_01_archive.html
http://www.examiner.com/article/blood-of-jesus-found-on-ark-of-the-covenant-scientific-proof-of-virgin-birth
http://www.natureworldnews.com/articles/9220/20140929/genetic-arms-race-helped-shape-human-genome.htm
http://www.mychristianmind.com/articles-2/the-soul-explained/
http://www.gotquestions.org/souls-created.html
http://www.ispor.org/vision2020.asp
https://www.youtube.com/watch?v=S-oxaW9-5WQ - UN base at bottom of Mt. Hermon.
https://www.ourinternet.org/#press/global-commission-on-internet-governance-iana-transition
https://www.ourinternet.org/media/publications/gcig_paper_no3.pdf
http://www.naharnet.com/stories/en/157876-u-s-panel-fails-to-lift-ban-on-gay-blood-donors
http://globalbiodefense.com/2014/12/03/consortium-pursue-ebola-convalescent-plasma/
http://globalbiodefense.com/2014/12/02/how-zmapp-therapy-attacks-ebola-virus/
http://www.occupycorporatism.com/home/googles-23andme-makes-easier-perfect-child/
https://www.ll.mit.edu/news/DRACO.html
http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0022572
http://en.wikipedia.org/wiki/DRACO_%28antiviral%29
http://www.33rdsquare.com/2013/09/anti-viral-drugs-may-soon-be-available.html
http://www.gwern.net/docs/1999-bradbury-matrioshkabrains.pdf
http://www.draper.com/newsItems.html
http://www.draper.com/emailedAnnouncements.html#nanotech_influenza
http://www.topictimes.com/videos/news/new-proof-funvax-was-real!!!,-genetic-manipulation-through-chemtrails-full-7DIK4qrPfU8.html
http://www.youtube.com/watch?v=XTdxFwi8L4g -- Mark of the Beast, Anti-Soul Vaccinations, and Your Salvation
http://www.braininitiative.nih.gov/BRAIN-Brochure.pdf
http://www.braininitiative.nih.gov/index.htm
https://www.docphin.com/research/medical-research-article-published-in-month.aspx?month=7&year=2003&page=2
http://whsc.emory.edu/home/publications/health-sciences/update/2014/july/hsu-july-2014.html
http://motherboard.vice.com/tag/BRAIN+initiative
http://www.rdmag.com/news/2014/01/new-nanotechnology-%E2%80%9Ctraps%E2%80%9D-viruses-they-infect-host-cells
http://www.topictimes.com/videos/howto/spiritual-root-of-blood-types-full-qyNmNLO6eSs.html
http://www.niaid.nih.gov/topics/BiodefenseRelated/Biodefense/Pages/DRACO.aspx
http://www.godlikeproductions.com/forum1/message1620333/pg4
http://jeb.biologists.org/content/216/1/127.full
http://www.scientificamerican.com/article/let-s-talk-about-ebola-survivors-and-sex/
http://www.who.int/csr/disease/ebola/faq-ebola/en/
http://www.openbible.info/topics/mark_of_the_beast
http://www.douglashamp.com/how-the-mark-of-the-beast-will-rewrite-the-human-genome-part-three-corrupting-the-image/
https://hwaairfan.wordpress.com/2012/06/30/eugenics-and-the-worlds-first-gm-babies/
https://funvax.wordpress.com/
http://www.shiningworld.com/Home%20Page%20Links/The%20God%20Gene.htm
http://pubchem.ncbi.nlm.nih.gov/compound/cytosine#section=Related-Records
http://www.princeton.edu/~achaney/tmve/wiki100k/docs/Cytosine.html
http://web.pdx.edu/~tothm/religion/Is%20God%20in%20Our%20Genes.pdf
http://www.ncbi.nlm.nih.gov/pubmed/23410751
http://web.pdx.edu/~tothm/religion/
http://threes.com/index.php?option=com_content&view=article&id=2206:the-god-gene&catid=81:religion&Itemid=61
http://www.ncbi.nlm.nih.gov/pubmed/18782654
https://books.google.com/books?id=nKRphq7s7x0C&pg=PA56&lpg=PA56&dq=removing+the+God+gene&source=bl&ots=mdQCfDk00&sig=Narh1JZepi5dttFH6Pmzh05FP3k&hl=en&sa=X&ei=r5uHVP_1JsHvUuujgfAG&ved=0CDIQ6AEwBDgU#v=onepage&q=removing%20the%20God%20gene&f=false
https://www.google.com/search?q=dracos&ie=utf-8&oe=utf-8&aq=t&rls=org.mozilla:en-US:unofficial&client=firefox&channel=fflb#q=draco+antiviral&rls=org.mozilla:enUS:unofficial&channel=fflb&start=10
http://www.theverge.com/2012/4/11/2940938/todd-rider-draco-doomsday-device-virus
http://www.nvic.org/CMSTemplates/NVIC/pdf/Live-Virus-Vaccines-and-Vaccine-Shedding.pdf
http://www.biblrytr.com/revelation14.htm
http://www.plospathogens.org/article/info%3Adoi%2F10.1371%2Fjournal.ppat.1003146
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3573120/
http://www.geovax.com/news-events/entry/2014/10/02/geovax-announces-initiation-of-ebola-vaccine-development-program.html
http://www.nvic.org/vaccines-and-diseases/Ebola.aspx
http://blog.adw.org/2010/08/why-is-the-first-sin-called-the-sin-of-adam-not-the-sin-of-adam-and-eve/
http://harmonicresolution.com/index.html
http://harmonicresolution.com/Manifestation%20Cycle.htm
http://www.dtic.mil/get-tr-doc/pdf?AD=ADA259077
http://www.dtic.mil/dtic/
http://news.nationalgeographic.com/news/2013/13/130310-extinct-species-cloning-deextinction-genetics-science/
http://nautil.us/issue/18/genius/super_intelligent-humans-are-coming
http://www.livestrong.com/article/62774-sperm-produced/
http://christianity.stackexchange.com/questions/7412/how-is-original-sin-transmitted
http://blog.adw.org/2010/08/why-is-the-first-sin-called-the-sin-of-adam-not-the-sin-of-adam-and-eve/
http://www.harmonicresolution.com/AbsoluteScaleFeatures.htm
http://www.harmonicresolution.com/ArchivesPage.htm
http://www.panspermia.org/virus.htm
http://www.timeenoughforlove.org/Virus.htm
http://www.evolutionnews.org/2014/05/panspermia_envi085801.html
http://www.buzzle.com/articles/is-there-life-on-other-planets.html
http://www.panspermia.org/whatsnew78.htm
http://www.pbs.org/wgbh/nova/tech/artificial-life.html
http://genotopia.scienceblog.com/337/is-eugenics-ever-okay/
http://libgallery.cshl.edu/items/show/49681
http://www.wiringthebrain.com/2013/05/the-new-eugenics-same-as-old-eugenics.html?showComment=1368455558914#c5821418481283745282
http://www.theguardian.com/science/2013/oct/13/craig-ventner-mars
http://www.genomics.cn/en/navigation/show_navigation?nid=2685
http://www.bab-genomics.com/list.aspx?catid=157
http://www.wiringthebrain.com/2013/05/the-new-eugenics-same-as-old-eugenics.html?showComment=1368455558914#c5821418481283745282
http://libgallery.cshl.edu/items/show/49681
http://thewertzone.blogspot.com/search/label/j.r.r.%20tolkien
http://tolweb.org/tree/
http://www.bibliotecapleyades.net/ciencia/ciencia_synchronicity.htm
https://www.emptywheel.net/2014/10/25/dna-sequence-analysis-shows-ebola-outbreak-naturally-ocurring-not-engineered-virus/
http://www.naharnet.com/stories/en/157876-u-s-panel-fails-to-lift-ban-on-gay-blood-donors