View Full Version : "Bringing The (Bio) War Home"

Ed Jewett
08-03-2009, 02:16 AM
Sunday, August 2, 2009

Bringing the (Bio) War Home (http://antifascist-calling.blogspot.com/2009/08/bringing-bio-war-home.html)

from anti-fascist calling blogspot

The 2001 anthrax attacks underscore the dangers posed to our health and safety by the Bioweapons-Industrial Complex.

The killer(s) employed a military-grade version of the deadly pathogen, a four-mutation blend of anthrax prepared at the government's test site at the remote Dugway Proving Ground in Utah. Based on available evidence it's a near certainty that the weapon came from stockpiles at the U.S. Army Medical Research Institute of Infectious Diseases (USAMRIID) in Ft. Detrick, Maryland.

Before the dust cleared prominent opposition politicians had been attacked, five people were murdered, 10,000 more were exposed and representative government ground to a halt as panic set in.

According to multiple media reports, federal investigators concluded that the anthrax spores in the letters addressed to former Senate leader Tom Daschle (D-SD) and Senate Judiciary Chairman Patrick Leahy (D-VT) could only have been produced in a state-run lab. The weaponized version of the pathogen contained as many as one trillion spores per gram, a concentration sufficient enough to kill half the American population if widely distributed.

But rather than giving pause to Pentagon weaponeers, Big Pharma who profit handsomely from vaccine production, the $100 billion agribusiness empire that drives research and the politicians who do their bidding, decades-long U.S. biowar programs have miraculously morphed overnight into a new growth industry: "biodefense."

What had once been Washington's dirty little secret has now blossomed into a $50 billion cash-cow for academic and corporate grifters, according to the Washington, D.C.-based Center for Arms Control and Non-Proliferation (http://www.armscontrolcenter.org/policy/biochem/articles/fy09_biodefense_funding/).

As the Bulletin of the Atomic Scientists (http://www.thebulletin.org/web-edition/columnists/laura-h-kahn/biosecurity-lessons-the-bruce-ivins-case) pointed out last year, "massive U.S. biodefense spending and a buildup of high-containment laboratories throughout the country might have created an internal security risk that no outside terrorist group could ever duplicate. Nearly two dozen new federal and many more new private biosafety level 3 and 4 laboratories have been built in recent years, meaning a large cadre of scientists has access to extraordinarily lethal material."

Indeed, under the auspices of the Department of Homeland Security (DHS), the new National Biodefense Analysis and Countermeasures Center (NBACC (http://www.nbacc.net/index.html)) opened in 2008 at USAMRIID. The center conducts inherently dual-use classified research and is currently managed by the spooky Battelle National Biodefense Institute.

Under the rubric of preventing bioterrorism, one question that DHS has not answered is whether or not government scientists and private contractors will conduct illicit experiments that violate the Biological Weapons Convention?

We may never know. Claiming that research will not breach the BWC, DHS avers that a "Compliance Review Group" overseen by senior Homeland Security officials will monitor NBACC operations. However information, including the Review Group's reports on Center operations or accidents at the facility may not be available under the Freedom of Information Act under cover of national security.

While it is reasonable to protect the nation's food supply from mischief, including sabotage by terrorists or deranged individuals armed with dangerous pathogens, work on animal diseases should be done transparently and safely. This however, is not the approach favored by the Department of Homeland Security.

A culture of secrecy and cover-up permeates the agency; after all DHS answers to the militarized Office of the Director of National Intelligence (ODNI), the so-called security "czar" who oversees the 16-agency U.S. intelligence complex.

"Food security" under such conditions is hardly amenable to public accountabilty; it is however, a formula that can be highly detrimental to our health, safety and well-being.

National Bio and Agro-Defense Facility

When the Department of Homeland Security announced plans to phase out the Plum Island Animal Disease Center (PIADC) by 2015, the agency cited (http://www.dhs.gov/files/labs/editorial_0762.shtm) the need to "enhance our nation's capacity to assess potential threats to humans and animals alike."

Averring that the Plum Island facility "is near the end of its lifecycle" and "is too small to meet the nation's research needs," DHS now plans to open the National Bio and Agro-Defense Facility (NBAF) on the campus of Kansas State University in Manhattan, Kansas. Estimated to cost taxpayers some $700 million to construct, the department plans to have the site up-and-running by 2014.

The authority for building the new facility comes from Homeland Security Presidential Directive 9 (HSPD-9 (http://www.dhs.gov/xabout/laws/gc_1217449547663.shtm)): Defense of Agriculture and Food. HSPD-9 mandates that the secretaries of Homeland Security, Agriculture, and Health and Human Services; the administrator of the Environmental Protection Agency and the heads of other "appropriate" federal departments and agencies "in consultation" with the director of the Office of Science and Technology Policy, "accelerate and expand the development of countermeasures against the intentional introduction or natural occurrence of catastrophic animal, plant, and zoonotic diseases."

According to a 2007 report (http://www.dtic.mil/cgi-bin/GetTRDoc?AD=ADA481366&Location=U2&doc=GetTRDoc.pdf) by the Congressional Research Service:

The DHS foresees multiple uses and goals for the new facility: serving as a unique BSL-3 and BSL-4 livestock laboratory capable of developing countermeasures for foreign animal diseases; providing advanced test and evaluation capability for threat detection, vulnerability assessment, and countermeasure assessment for animal and zoonotic diseases; and supporting countermeasure licensure.

The research agenda for NBAF is to be at least partially based on current risk assessments and subject to change as the risk assessments change. The DHS predicts that the facility will focus on foot and mouth disease (FMD), classical swine fever, African swine fever, Rift Valley fever, Nipah virus, Hendra virus, contagious bovine pleuropneumonia, and Japanese encephalitis. (Dana A. Shea, Jim Monke and Frank Gottron, The National Bio- and Agro-Defense Facility: Issues for Congress, Congressional Research Service, RL42160, November 15, 2007)A zoonotic disease is one that can easily be transmitted from animals to humans; examples include Rift Valley fever, Lyme Disease, West Nile virus, H1N1 and H5N1 influenza. These pathogens however, can also be deployed as plausibly deniable bioweapons, a point not addressed by government investigators.

"Countermeasure licensure" of course, is a formula for handing over the fruit of publicly funded research to unaccountable private corporations who stand to make hefty profits from the manufacture of vaccines.

More pertinently, will America's expanding "biodefense" industry serve as a cover for the manufacture of new weapons of war?

As Watergate-era congressional investigations and multiple media reports have conclusively demonstrated, for decades the Central Intelligence Agency and the Pentagon employed far-right Cuban mercenaries to attack the economic and agricultural infrastructure of socialist Cuba.

Indeed, Newsday reported (http://www.thepeoplesvoice.org/TPV3/Voices.php/2009/04/28/cia-link-to-cuban-pig-virus-reported) as far back as 1977, that "operatives linked to anti-Castro terrorists introduced African swine fever virus into Cuba in 1971. Six weeks later, an outbreak of the disease forced the slaughter of 500,000 pigs to prevent a nationwide epidemic."

The African swine fever virus deployed in the attack according to participants, was believed to have originated from stockpiles stored at the Plum Island Animal Disease Center and handed over to CIA-trained terrorists at Ft. Gulick, an Army base in the former Panama Canal Zone.

And in 1981 according to researcher William H. Schaap, Cuba was struck by a devastating epidemic of Dengue fever, "one of some 250 arthropod-borne viruses, or 'arboviruses,' diseases transmitted from one vertebrate to another by hematophagous arthropods--blood eating insects, usually mosquitoes."

"Dengue and other arboviruses" Schaap wrote, "are ideal as biological weapons for a number of reasons. Dengue, especially hemorrhagic dengue, is highly incapacitating; it can be transmitted easily through the introduction of infected mosquitoes; it will spread rapidly, especially in highly populated and damp areas."

Citing the simultaneous outbreak of the disease in three widely separated parts of Cuba and that it is "extremely unusual that such an epidemic would commence in three localities at once," and the absence of the disease on adjacent islands such as Haiti and the Dominican Republic, Schaap concludes that the pathogen was purposely introduced into Cuba as a bioweapon.

Indeed, Army researchers at Ft. Detrick had conducted dispersal studies of the Aedes aegypti mosquito--and Dengue fever--used in the 1981 attack against the island nation.

The epidemic which hit Cuba in May 1981 was of type 2 dengue with hemorrhagic shock. Except for the type 1 epidemic reported in 1977, this was the first major dengue outbreak in Cuba since 1944, and, most importantly, the first in the Caribbean since the turn of the century to involve hemorrhagic shock on a massive scale.

From May to October 1981 there were well over 300,000 reported cases, with 158 fatalities, 101 involving children under 15. At the peak of the epidemic, in early July, more than 10,000 cases per day were being reported. More than a third of the reported victims required hospitalization. By mid-October, after a massive campaign to eradicate Aedes aegypti, the epidemic was over. (William H. Schaap, "The 1981 Cuba Dengue Epidemic," Washington, D.C.: Covert Action Information Bulletin, Number 17, Summer 1982)And if the past is any guide to future actions by the Pentagon and the so-called Intelligence Community, what can we infer from DHS's stated goal of standing-up NBAF as a center for assessing "potential threats to humans and animals alike"? As it turns out, quite a lot.

Government Accountability Office (GAO) investigators charge that DHS relied on "a rushed, flawed study" to justify its decision to locate the $700 million research facility for highly infectious pathogens "in a tornado-prone section of Kansas, according to a government report," The Washington Post reported (http://www.washingtonpost.com/wp-dyn/content/article/2009/07/26/AR2009072602857.html) July 26.

The dubious report in question, United States Department of Agriculture Biocontainment Feasibility Studies, Study Report: Plum Island Animal Disease Center, was commissioned by the U.S. Department of Agriculture (USDA) and prepared by the giant defense and security firm Science Applications International Corporation (SAIC (http://www.saic.com/)).

Talk about feathering one's own nest! SAIC's Frederick, Maryland advanced technology division (near Ft. Detrick) has partnered-up with with a host of federal agencies including the U.S. Army Medical Research Institute for Infectious Diseases, the Pentagon's primary biowarfare research center.

Needless to say, the spooky firm has considerable clout in Washington. According to Washington Technology's "2009 Top 100 Federal Prime Contractors" list (http://washingtontechnology.com/toplists/top-100-lists/2009.aspx), SAIC clocks-in at number 7 (just behind KBR Inc.) with some $4,811,194,800 in revenue, the bulk of earnings coming from defense and security contracts with the federal government.

Last year however, a preliminary GAO report (http://energycommerce.house.gov/images/stories/Documents/Hearings/PDF/Testimony/OI/110-oi-hrg.052208.Kingsbury-Testimony.pdf) was unveiled during hearings before Congress' Subcommittee on Oversight and Investigations, Committee on Energy and Commerce. It was highly critical of the flawed reasoning behind DHS's NBAF decision and SAIC's report. Relying on USDA's 2002 study, GAO auditors found that the agency,

has neither conducted nor commissioned any study to determine whether work on foot-and-mouth disease (FMD) can be done safely on the U.S. mainland. Instead, in deciding that work with FMD can be done safely on the mainland, DHS relied on a 2002 U.S. Department of Agriculture (USDA) study that addressed a different question. The study did not assess the past history of releases of FMD virus or other dangerous pathogens in the United States or elsewhere. It did not address in detail the issues of containment related to large animal work in BSL-3 Ag facilities. It was inaccurate in comparing other countries' FMD work experience with that of the United States. Therefore, GAO believes DHS does not have evidence to conclude that FMD work can be done safely on the U.S. mainland. (Nancy Kingsbury, Managing Director Applied Research and Measurements, Government Accountability Office, High-Containment Laboratories: DHS Lacks Evidence to Conclude That Foot-and-Mouth-Disease Research Can Be Done Safely on the U.S. Mainland, Testimony Before the Subcommittee on Oversight and Investigations, Committee on Energy and Commerce, House of Representatives, May 22, 2008, GAO-08-821T)The SAIC review addressed a different issue: whether or not it is "technically feasible" to conduct such research on the U.S. mainland. GAO averred, "This approach fails to recognize the distinction between what is technically feasible and what is possible, given the potential for human error."

Citing "methodological problems" in SAIC's study, GAO auditors found that the report: "(1) did not assess the history of releases of FMD virus or other dangerous pathogens, (2) did not address in detail the issues related to large animal work in BSL-3 Ag facilities, and (3) was inaccurate in comparing other countries' FMD work experience with that of the United States."

GAO concluded that among the report's more glaring and obvious problems, "(1) the study used an ad hoc method to select its expert panel that was not necessarily free from bias; (2) the study report was written by a single third-party person under contract for that purpose who was not present during the panel discussions; and (3) no concern was taken to ensure that the expert panel members reviewed either the draft or the final version of the report. At least one expert panel member expressed disappointment with the slant of the report."

Indeed, the SAIC review failed to address the issue of past releases of FMD or other pathogens, nor did it assess "the general history of accidents within biocontainment facilities." No small matter when it comes to potential mischief or lax safety standards known to exist at such facilities.

According to GAO, "the study panel members we interviewed said that no data on past accidents with or releases of either FMD or other pathogens was systematically presented or discussed. Rather, the panel members recalled that they relied on their own knowledge of and experience with the history of releases in a general discussion."

In a follow-up report (http://www.gao.gov/new.items/d09747.pdf) published in July 2009, GAO discovered that DHS's Environmental Impact Statement (EIS) was wholly inadequate and in fact, relied on flawed and outdated methodology to arrive at their conclusions. According to GAO auditors "Comments on the NBAF draft EIS included the following concerns:"

* the ability of DHS and the federal government in general to safely operate a biosafety facility such as the proposed NBAF;
* the potential for a pathogenic release through accidents, natural phenomena, and terrorist actions;
* our May 2008 testimony that concluded that DHS had not conducted or commissioned a study to determine whether FMD research could be conducted safely on the U.S. mainland;
* natural phenomena such as tornadoes, earthquakes, and hurricanes that could cause catastrophic damage to the NBAF and result in the release of a pathogen;
* the possibility that an infected mosquito vector could escape, allowing a pathogen such as Rift Valley Fever virus to become permanently established in the United States;
* the economic effects of a release or a perceived release on the local, state, and national livestock industry. (United States Government Accountability Office, Report to Congressional Committees, Biological Research: Observations on DHS's Analyses Concerning Whether FMD Research Can Be Done as Safely on the Mainland as on Plum Island, July 2009, GAO-09-747)Indeed similar to the earlier USDA study, DHS's EIS failed to include even a cursory analysis of multiple releases of the FMD virus at Plum Island itself. No matter, full speed ahead!

Leading the charge to site NBAF at Kansas State University is the Kansas Bioscience Authority (KBA (http://www.kansasbioauthority.org/)), a business and academic consortium chaired by former Democratic governor John Carlin. Plush with industry heavy-hitters such as the Midwest Research Institute (MRI (http://www.mriresearch.org/)), the lobby shop KansasBio (http://www.kansasbio.org/), Symark LLC (http://www.symarkllc.com/), a technology commercialization firm specializing in the biosciences industry, KBA is hell-bent on bringing NBAF to Kansas despite serious health and safety concerns.

According to a Kansas City Star report (http://www.kansascity.com/637/story/1349759.html), Tom Thornton, the President and CEO of the Kansas Bioscience Authority told the newspaper "This nation needs to have one modern biocontainment lab that conducts research into these diseases to protect agriculture and protect public health."

Claiming that the GAO report was "biased," KBA's John Carlin asserted that "aside from using Dorothy as their science, they don't have much going for them." Thornton said the project would be built as a "vault inside a vault inside a submarine" to protect against the accidental release of germs and diseases.

In other words, move along...

DHS and USDA assert, despite historical evidence, that Foot-and Mouth-Disease (FMD) as well as research with other dangerous pathogens can be safely conducted on the U.S. mainland at its new agro-defense center. But if evidence from Britain is any guide on what to expect, the explosive growth of Biosafety Level 3 and 4 laboratories in the United States will only compound the problem.

In 2001 and 2007, FMD releases at Britain's Institute for Animal Health at Pirbright were traced to a leaking drain which allowed the disease to escape containment. Crumbling infrastructure is only one of a constellation of issues that led to the outbreaks, investigators discovered. Lax oversight and a culture of secrecy nearly devastated Europe's livestock.

According to Britain's National Audit Office (http://www.nao.org.uk/publications/0102/the_2001_outbreak_of_foot_and.aspx), the direct cost of the 2001 outbreak to the public sector was estimated at over $5.71 billion and the cost to the private sector clocked-in at over $9.51 billion. Indeed, when tourism and supporting industries were factored into the equation, total losses ballooned from $8.56 billion to $10.27 billion when movement into the countryside was restricted by the state, UK auditors estimated.

By the time FMD was eradicated in September 2001, more than six million animals had been slaughtered and the disease had spread to France, the Republic of Ireland, the Netherlands and Northern Ireland. A similar outbreak in 2007 fueled calls to close the facility.

This is not a problem confined to Britain, but is endemic to the entire bioweapons and "biodefense" complex globally, particularly here in the heimat.

Tip of a Sinister Iceberg

Bioweapons research, secrecy and contamination go hand in hand.

Despite soothing bromides from defense corporations, the military, the scientific community and the politicians who do their bidding, the accidental or planned release of selected pathogens into the environment for "research purposes" is an enduring legacy of America's Cold War biowar programs.

The experimentation on witting and unwitting subjects in a score of top secret Army and CIA programs underscore the sinister nature of the Bioweapons-Industrial Complex. Indeed, a 1994 GAO report (http://archive.gao.gov/t2pbat2/152601.pdf), documented:

During World War II and the Cold War era, DOD and other national security agencies conducted or sponsored extensive radiological, chemical, and biological research programs. Precise information on the number of tests, experiments, and participants is not available, and the exact numbers may never be known. However, we have identified hundreds of radiological, chemical, and biological tests and experiments in which hundreds of thousands of people were used as test subjects. These tests and experiments often involved hazardous substances such as radiation, blister and nerve agents, biological agents, and lysergic acid diethylamide (LSD). In some cases, basic safeguards to protect people were either not in place or not followed. For example, some tests and experiments were conducted in secret; others involved the use of people without their knowledge or consent or their full knowledge of the risks involved. (Frank C. Conahan, Assistant Comptroller General, National Security and International Affairs Division, Human Experimentation, An Overview on Cold War Era Programs, General Accounting Office, September 28, 1994, GAO/T-NSIAD-94-266)Despite efforts since the Watergate-era to uncover the extent of these programs, many remain classified to this day. The GAO found that the Central Intelligence Agency, more concerned with shielding their corporate partners' participation in illicit experiments with LSD and other psychoactive compounds "have made little effort to assist test participants by identifying test locations and participants in experiments conducted by contractors." The Agency "in fact, has not released the names of 15 of the approximately 80 organizations that conducted experiments under the ... MKULTRA program because the organizations do not want to be identified."

One sinister Pentagon project, Operation WHITECOAT, was a secret U.S. Army weapons' testing program carried out between 1954-1973 on Seventh-day Adventist Church conscientious objectors who consented to the experiments, and over 2,300 Army soldiers who almost certainly were not provided anything approaching informed consent. Similar to cattle, sheep or pigs on Plum Island, test subjects were infected with agents such as Q Fever, yellow fever, Rift Valley fever, Hepatitis A, bubonic plague, Tularemia (rabbit fever) and Venezuelan Equine encephalitis.

Indeed, the range of experimentation on human subjects carried out by the U.S. biological weapons program makes for a very grim read. As Boston College sociologist Jeanne Guillemin wrote in her disturbing exposé,

The entire experimental legacy is dismaying, from the hundreds of dead monkeys at Fort Detrick to the spectacle of Seventh Day Adventist soldiers, the vaccinated volunteers in Project Whitecoat, strapped to chairs amid cages of animals in the Utah sunlight as Q fever aerosols are blown over them. Most chilling are the mock scenarios played out in urban areas: light bulbs filled with simulated BW agents being dropped in New York subways, men in Washington National Airport spraying pseudo-BW from briefcases, and similar tests in California and Texas and over the Florida Keys. (Jeanne Guillemin, Anthrax: The Investigation of a Deadly Outbreak, Berkeley: University of California Press, 1999, pp. 176-177.)As Michael Christopher Carroll's stunning investigation of Plum Island, Lab 257 (http://www.harpercollins.com/books/9780060781842/Lab_257/index.aspx) revealed, multiple releases of highly-contagious pathogens including Foot-and-Mouth-Disease and Rift Valley Fever, were systematically covered-up by the USDA and DHS.

Will it be any different at the new National Bio and Agro-Defense Facility? If one were to believe DHS, it would represent the triumph of hope over experience. This is not a rational starting point when it comes to experiments with highly-contagious pathogens.

America's corporate media however, seemingly impermeable to anything other than celebrity scandals and the crimes of official enemies, refuse to conduct in-depth investigations into the expansion of America's Bioweapons-Industrial Complex.

Despite government pronouncements, faithfully regurgitated by media stenographers to the public, available evidence suggests that the United States, as in the past, is pursuing the development of biological agents for use in a score of clandestine weapons programs.

Under cover of conducting research on the highly-contagious Foot-and-Mouth-Disease pathogen, a new and improved national laboratory equipped with BSL-3 and BSL-4 containment facilities, like their cohorts at the U.S. Army Medical Institute of Infectious Diseases at Ft. Detrick, Maryland in all probability will continue to investigate the efficacy of waging aggressive biological warfare on an adversary's food supply.

Sound far-fetched? If the evidence from Cold War-era CIA and Pentagon programs, well-documented accidents, illicit human experimentation as well as numerous examples of biological attacks against socialist Cuba are a guide to Washington's future behavior, better think again!


Jack White
08-03-2009, 02:32 AM
August 1, 2009
New Evidence: That The ‘Swine Flu’ Pandemic Is Man-Made
Filed under: World — Tags: flu, Pandemic, swine flu — Satinder SINGH @ 7:36 am
Murder suspects are either convicted or acquitted at trial based on the prosecution’s presentation of EVIDENCE which usually hinges on MOTIVE, OPPORTUNITY, and TIME-LINES combined with physical documents. To gather such hard evidence, detectives and/or federal agents often spend months following leads and interviewing witnesses. In the trial phase, re-creating the sequence of events is essential. I submit this paper will provide more than enough hard evidence to at least result in a series of criminal indictments of charges of MASS MURDER, and CONSPIRACY TO COMMIT WORLD GENOCIDE against Novartis Pharmaceutical principals and agents and others.


The Primary Motive behind this alleged criminal activity is also the primary cause of most murders in the world today, and that motivation is simply: BIG MONEY. Billions of Dollars of windfall profits from government contracts worldwide, as a matter of fact.
I will provide evidence that will show that Novartis Pharmaceuticals of Basel, Switzerland has conspired with corrupt “scientists” at the U.S. Army Institute of Pathology Ft. Detrick, Maryland, to create a “novel” strain of weaponized “influenza” virus by means of “reverse engineering” the deadly 1918 killer strain which strain was maliciously and surreptitiously released upon the world in March and April of 2009 for the primary purpose of creating a panic-stricken world-wide demand for Novartis vaccine material.

The evidence will also clearly show that the Novartis vaccine material is in reality designed to facilitate the further mutation of the pandemic into more lethal waves of increasingly virulent and deadly disease, rather than to curtail and limit the existing outbreak. The evidence will show that Novartis is willingly being used, (and extremely well-paid) to facilitate the edicts of the global elite’s Club of Rome; which edicts clearly call for a massive and sudden depopulation of certain segments of the earth’s human population.


To realize such windfall profits on an engineered, global flu pandemic, detailed covert planning must take place of course.
Patents protecting the proprietary flu vaccine must be applied for and secured before the pandemic virus is released in order to minimize the competition and maximize the profit potentials. In a biological attack of this nature, timing is extremely critical.
Indeed, the evidence is clear Novartis applied for just such a patent on Nov. 4, 2005, and the U.S. Patent Office accepted this application and granted US 20090047353A1 for a “Split Influenza Vaccine with Adjuvants” on February 19, 2009. (See bottom of page).

With this patent now secured, the conspirators were now free to create the demand for their “novel” split influenza vaccine by releasing a “novel” split-influenza (combining multiple viruses) pandemic virus from a weapons lab test-tube into unsuspecting human hosts. http://www.washingtonpost.com/wp-dyn/content/article/2009/06/17/AR2009061703271.html

The so-called “Swine Flu” grabbing headlines today is actually a recombinant, or “split-influenza” virus consisting of A-strain Bird-Flu (H5N1), Swine Flu (H1N1) and multiple strains of human flu (H3N2). Likewise, the 1918 Killer Flu that killed untold millions of people was a recombinant or “split-influenza” virus composed of Bird flu, Swine Flu, and multiple strains of human flu.


The criminal timeline begins in 1997, when Dr. Jeffrey Taubenberger assembled a team of geneticists and microbiologists to analyze the genome structure, and then to REPRODUCE (i.e. reverse engineer) what is arguably one of the most deadly viral structures the world has ever been cursed with the 1918 killer flu virus. According to numerous published stories and reports, Taubenberger and his team utilized super-computers to map the complex RNA and DNA structures of the killer virus, then utilized human plasmids to successfully re-create the 1918 killer. Taubenberger completed his work in early 2005, then immediately left the employ of the U.S. Army at Ft. Detrick to take a much more lucrative position with the National Institutes of Health. His new focus was to create a VACCINE against the very same 1918 killer flu that he and his team had, just months earlier, successfully “reverse engineered” and created.

This researcher is very confident that a focused criminal investigation would likely reveal prima facia evidence that Taubenberger was in reality working for Novartis while employed with the N.I.H. and was quite likely the primary author of Novartis’ Nov. 6, 2005 “provisional” patent application. On page 2, paragraph 32 of the patent publication we read, quote: “The influenza virus [that the 'invention vaccine' is designed to protect against] may be a reassortant strain, and may have been obtained by reverse genetics techniques. Reverse genetics techniques allow influenza viruses with desired genome segments to be prepared in vitro using plasmids.” The remnant of the paragraph then goes into very specific detail as to the actual mechanics of how the pandemic virus was actually created by Taubenberger’s Ft. Detrick team. At the very least, the author of the patent application had to have studied Taubenberger’s various published reports on his work at Detrick, for the wording and science is virtually verbatim.

Furthermore, this paragraph is even more damning by the words “may have been obtained”. Who “obtained” this virus and for what reason was it “obtained”? Keep in mind the CDC and HHS would have Americans believe that the pandemic viral outbreak is totally a “natural” occurrence if so then how could Novartis have such an incredible advance knowledge to the point of developing a vaccine with such absolutely PERFECT TIMING???


Novartis International AG is simply the world’s largest, multi-national pharmaceutical company with over $53 Billion USD revenue generated in 2008. It’s headquarters is located in Basel, Switzerland, home of the vaunted “Swiss Guards” who provide all security measures for the Vatican and the Club of Rome. The company logo symbolizes the “eternal flame” of the Illuminati “enlightened ones”. Dig into Novartis International AG’s long history, and one finds that it began as a component of the infamous I.G. Farben combine, which in turn was primarily responsible for the rise of Adolph Hitler and the German/Austrian Third Reich.

Dig a bit deeper and you find that Novartis also wholly owns a company called Sandoz which was the inventor of LSD and other strong hallucinogenic “truth” drugs, and was the supplier of LSD to the CIA allowing them to scale new heights with their covert “MK ULTRA” mind control experiments. Documents released to U.S. Congressional investigators in 1977 show that Sandoz Labs had arranged for certain Nazi scientists to gain new identities in Allen Dulles’ CIA at the conclusion of WWII. This was accomplished under a secret extraction program called “Operation Paper Clip”.

The address listed on the Novartis Patent applications is a P.O. Box in Emeryville, California. Up until the summer of 2005, this Emeryville California address belonged to Chiron Inc. the world’s second-largest INFLUENZA VACCINE MANUFACTURER. Chiron was doing very well, with reported sales of $357 million in fiscal 2002. Chiron’s sales nearly doubled, peaking at a whopping $678 million in 2003 and it was mostly due to the marketing and sale of FLU VACCINE CONTRACTS to the federal government. Novartis, which owned much of Chiron’s stock, was very pleased, until disaster struck in 2004 — the entire year’s stock of flu vaccine was found to be contaminated and was condemned.

Stock values plummeted on the news. With the stock at a historic low, Novartis quickly purchased the remainder of Chiron’s stock and began immediately to work on the massive “novel pandemic flu” vaccine that they somehow knew would soon have worldwide demand especially if they controlled the exclusive patent they could effectively “corner the pandemic flu vaccine market”!!


I would submit that killing tens of thousands of innocent humans via the systemic creation of a “pandemic” in order to make billions of dollars is vile enough, but there is also evidence that there is an even more heinous hidden agenda at work here, and it is spelled GENOCIDE.

It is no mystery that Adolph Hitler advocated the elevation of a Nordic “Master Race” that would rule the world in a “New Order of the Ages” called the “Third Reich”. Sadly, not all of the EUGENIC/GENOCIDAL National Socialists were executed at Nuremburg.
In reality, the elite financiers that actually dictated the agenda to Hitler, merely went underground, willing to bide their time until their godless agenda to liquidate BILLIONS of people could be successfully implemented.

The evidence that the Novartis-controlled “Pandemic Vaccine” may well be a tool of mass genocide, is actually quite overwhelming.
At this point, some readers may scoff and ask: “Why would any company want to kill off their customers?” The answer is that these “customers” control large blocks of assets and equity. As Kissinger’s “NSSM-200´´ report outlines, the “spoils” of genocide include controlling large tracts of land and mineral assets. This is secondary, of course, to their warped dream of creating a Utopian World Order with only 500 million “worthy” humans allowed to share in it.


While George H.W. Bush was busy saving the world from the evil dictator Saddam Hussein in 1991, pursuant to his U.N. speech to create a “new world order” an agenda for an “Initiative for Eco-92 Earth Charter” elitist meeting happened to fall into honest, Christian hands. This agenda basically reiterated the genocide outlined in Henry Kissinger’s infamous NSSM-200 report of 1974, and called for “the immediate reduction of world population.” The entire report can be downloaded at:

My extensive research shows that by 1992, the massive death rate of AIDS had simply not materialized to the Elite’s satisfaction, and a more efficient mass killer had to be engineered in order to fulfill the edicts cut into the “Georgia Guidestones”.

Evidence shows that like the 2009 “Novel” Flu Virus the HIV virus was also engineered and manufactured in the labs of Ft. Detrick.

In 1969, during a House Appropriations Committee hearing, the Defense Department’s Biological Warfare (BW) division at Ft. Detrick requested funds to develop, through complex gene-splicing (i.e. genetic engineering) a “novel” new disease that would both be resistant to, and break down a victim’s immune system. The Congressional Record reads:

“Within the next 5 to 10 years it would probably be possible to make a new infective micro-organism which could differ in certain important respects from any known disease-causing organisms. Most important of these is that it might be refractory to the immunological and therapeutic processes upon which we depend to maintain our relative freedom from infectious diseases.”

The funds for this “Dr. Strangelove” project were somehow approved. AIDS “magically” appeared within the requested time frame, and of course, just happens to exhibit the exact characteristics specified by the Ft. Detrick scientists.

Three years later, in 1972, the fledgling World Health Organization (WHO) published a very similar proposal to the one submitted to the U.S. House Appropriations Committee in 1969. The WHO proposed that: “An attempt should be made to ascertain whether viruses can in fact exert selective effects on immune function, e.g., by …affecting T cell function as opposed to B cell function. The possibility should also be looked into that the immune response to the virus itself may be impaired if the infecting virus damages more or less selectively the immune cells responding to the viral antigens.” (Bulletin of the W.H.O., vol. 47, p 257- 274.) This is a “textbook” clinical description of the function of the HIV/AIDS virus.

The W.H.O. shortly thereafter begins a massive “smallpox vaccination” program in Africa in 1975. Within two years, millions of smallpox vaccines are provided by Novartis et. al, under U.N.I.C.E.F. funding. A decade later, it is determined by independent journalists in the U.K. that the incidence of AIDS infections’ MAPPED AND GRAPHED EPICENTERS in Africa coincided exactly with the locations of the W.H.O. smallpox vaccination program centers in the mid-1970’s (Source, The London Times, May 11, 1987). Some 14,000 Haitians then on UN ‘humanitarian missions’ to Central Africa were also vaccinated in this campaign, and soon contracted HIV. Personnel actually conducting the vaccinations of the Haitians maintain they had been completely unaware that the vaccine was anything other than a routine shot.

In 1987, Dr. Hilleman, head of all vaccine production of Merck Pharmaceuticals stunned the world with his public admissions that the mass vaccination campaigns of the 1950s and ’60s likely caused thousands of cancer deaths each year. This was due to the presence of a cancer-causing virus that contaminated the first polio vaccine, according to Dr. Hilleman. Known as SV40, the virus originated from dead monkeys whose kidney cells were used to culture the first Salk vaccines. Doctors estimate that the virus was injected into tens of millions during the vaccination campaigns, including several million in Canada, before being detected and screened out in 1963. Those born between 1941 and 1961 are thought to be most at risk of having been infected with SV40, and are estimated to have a 300% greater chance of developing cancer. According to Hilleman MERCK KNEW THE VACCINES WERE INFECTED WITH SV40, but distributed them anyway. See http://www.youtube.com/watch?v=edikv0zbAlU

Furthermore, research doctors in New Orleans reported in 1963 that a percentage of the Salk polio vaccines were found to have attenuated, (live) viruses, which actually CAUSED tens of thousands of polio cases during the 1950’s.

Following the successful liberation of Kuwait in Operation Desert Storm, hundreds of thousands of victorious American troops are suddenly stricken with a wide variety of auto-immune disorders that doctors named the Gulf War Syndrome, (GWS). After a decade of medical investigation, the culprit is finally determined to be an ingredient in the anthrax vaccinations mandatorily given to the troops. This offending “adjuvant” is a synthetic material known as squalene aka, oil-in-water adjuvant. Writer and Gulf War correspondent Gary Matsumoto documents this entire, tragic saga in his seminal book, “Vaccine-A”. See www.vaccine-a.com.

Understanding these historical facts is very important for this reason: Those that ignore history are doomed to repeat it. This is doubly true when it comes to blindly accepting a “novel” mass vaccination for a weaponized, “reverse engineered” virus.

The historical record is very clear attenuated, live viruses in vaccines SPREAD the disease very effectively. When combined with SQUALENE ADJUVANT the virus becomes many times more potent and lethal. When given to CHILDREN IN SCHOOLS, millions of “typhoid Matts and Marys” will be spreading the disease exponentially.

Chillingly, the Novartis patent for the “novel pandemic flu” declares that “African green monkey kidney cells” will be used for the “viral growth substrate” i.e. the carrier medium.
(Page 3, paragraph 0037) We also see that “oil-in-water” squalene-based adjuvants will also be included (page 8 0098) but most incredible of all, because this is a “recombinant” and “novel” split vaccine, it is deemed necessary to include fragments of attenuated viruses (i.e. live pathogens) in the vaccine medium.

On July 13, 2009, the W.H.O. sanctioned this lunacy by declaring: “In view of the anticipated limited vaccine availability at global level and the potential need to protect against “drifted” strains of virus, it is recommended that promoting production and use of vaccines such as those that are formulated with oil-in-water adjuvants and live attenuated influenza vaccines is important.”

In conclusion and summation, it should be evident that the “2009 Swine Flu” could just as easily be called the “Bird Flu” because it is as much H5N1 (bird flu) as H1N1 (pig flu.) Novartis knew this in 2005 when it received hundreds of millions of dollars from Mike Leavitt’s HHS to develop and patent the “bird flu” vaccine. I publicly charge that Novartis had advance knowledge of this “combination” because they had been in consultation with Jeffrey Taubenberger for years.

It is further evident that Novartis’ patent provides for “influenza vaccine kits” to be provided to other pharmaceutical manufacturers as well. These “kits” are the basic raw ingredients needed for the other companies to build their own vaccines under their own label.

In 2005, this “jobbing” of separate ingredients by multiple companies would never have been allowed because of the legal liability issues involved. However, in 2009, all liabilities for death and disability from faulty or contaminated vaccines have been stripped away. Any wrongful death or disability lawsuits against Novartis or any other company will today be summarily dismissed.
Novartis today has carte blanche blanket immunity for their actions and any large pharmaceutical company who so desires, can join them at the feeding troughs just by paying millions for their “kits”.

If this isn’t the pinnacle of criminality, then I don’t know what is.

Novartis, if this “novel split vaccine” is so wonderful and safe, why do you require such blanket protection from litigation?


Ed Jewett
08-03-2009, 04:43 PM
August 1, 2009

Before you’re forced to get any mandatory vaccinations… (http://www.lewrockwell.com/blog/lewrw/archives/31532.html)

have the physician ordering it, or the physician recommending it, or your personal physician, read, fill out and sign a Physician's Warranty of Vaccine Safety form


and waive any statutory, Common Law, Constitutional, UCC, international treaty, and any other legal immunities from liability lawsuits.