lab origins of a h1n1 mexican frankenflu ... origins of a h1n1 mexican frankenflu & toxic...

LAB ORIGINS OF

A H1N1 MEXICAN

FRANKENFLU &

TOXIC EUGENIC

MANDATORY

VACCINESDR BILL DEAGLE MD

DABFP AAEM A4M

NUTRIMEDICAL.COM

LABVIRUS.COM BLOG

RESCUE FROM PANDEMIC FLU

& TOXIC VACCINES

WHO UN EUGENICS

POPULATION CONTROL

TIMETHEHIntroduction

Strategy

Challenges Forward3

2

1 ORIGINS OF PANDEMIC FLU

A H1N1

LABFLU

2009

H5N1

AVIAN

FLU

1997

1918

H1N1

SWINE

FLU

VACCINE MISHAP

& EUGENIC

BIOWEAPONS

LAB ORIGINS OF A H1N1SWINE FLU

1917 TYPHUS VACCINE SWINE FLU ORIGINS AS

RECOMBINANT SWINE AND HUMAN FLU

• DR HENRY L. NIMAN – DR BILL DEAGLE

MD AUGUST 2006 REVIEW OF PROOF

OF WSN33 OLDEST HUMAN AND IOWA

PIG FLU RECOMBINANT ORIGINS OF

1918 FLU

• TYPHUS VACCINE PASSED THROUGH

PIGS ON VACCINE FACILITY – FT.

LUPTON, KANSAS, USA

• SPONTANEOUS RECOMBINANT

INFECTED TROOPS HEADED ON AIR

TROOP TRANSPORTS TO SPAIN, WWI

RESURRECTION OF THE 1918

PANDEMIC SWINE FLU• 1951 US TEAM FAIL TO GROW VIRUS IN LAB

CULTURE FROM ALASKA EXUMED VICTUMS OF

1918 SWINE FLU

• 1997 MARCH 16TH – BASEL, SWITZERLAND -

HUMAN LIFE INTERNATIONAL PRIVATE BOARD

MEETING – 3 PROJECTS

• LATE 90s - DR TAUBENBERG PhD CDC – HEADS

TEAM TO USE PROMIS – ORACLE 8i

SUPERCOMPUTER SOFTWARE TO RESURRECT

GENE FRAGMENTS 1918 FLU – Ref: Dr True Ott

PhD ND

WHO UN GLOBAL EUGENICS

POPULATION PROJECTS:

• 1- PLAMID ANTI-HCG PLACENTAL

ABORTION VACCINATION – AFRICA,

PHILLIPINES AND SOUTH AMERICA

• 2 – SPECIAL VIRUS PROJECT –

MYCOPLASMA HOSTED RNA

RETROVIRUS – IMMUNE FAILURE AND

CANCER AIDS VIRUS

• 3 – RESURRECTED PANDEMIC FLU

1918 – AVIAN – SWINE BINARY

WEAPON

NOVARTIS PHARMA ORACLE 8i

VIRAL RESURRECTION • FOUR NATIONS – USA CDC, NIAID, USAMRID –

CANADA NATL MICROBIOLOGY, WINNIPEG, BRITAIN,

ISRAEL BIOWEAPONS NEGEV

• SUCCESSFUL RESURRECTION OF H1N1 NOVEL VIRUS

WSN33 HUMAN AND

• IOWA PIG FLU RECOMBINANT WITH NOVARTIS

ORACLE 8i SUPERCOMPUTER AND BIOENGINE GENE

SEQUENCER

• 2007 PATENT FOR NOVEL H1N1 VIRUS APPLICATION

• SOURCEs: 1997 HLI Zurich, Switzerland WHO

UN, and 2009 ResearchDr True Ott PhD ND &

Don Nicoloff – Novartis DayCart Daylight Oracle 8i

Supercomputer Predictive Software

BIOENGINEERED SUPERCOMPUTER

ORACLE 8i LABVIRUS PLAQUE FLU

• Novartis‟ patent specifically details that the viral

pathogen which the patented vaccine is designed

to protect against is a

• “Reverse Engineered” Designer Virus that could

only have been created in the labs of

• Ft. Detrick utilizing ORACLE 8i equipped

computers.

• EXACTLY what Michael Riconosciuto testified

about years earlier concerning the Biological

Warfare capabilities of ORACLE 8i software.

• Source: Dr True Ott PhD ND

VACCINE-INDUCED DISEASE

EPIDEMIC OUTBREAKS (V.I.D.E.O.s)

• The Engineering of “Pandemics”

• By A. True Ott, PhD, ND

• AMA, JOHN D ROCKEFELLER 1921

• PROOF ADVERTISERS PROTECTIVE BUREAU

KANSAS SMALLPOX VACCINE DISEASE EPIDEMIC

• VACCINES CONTAIN LIVE VIRUSES, ONLY WEAKENED

OR ATTENUATED THAT CAN CAUSE DISEASE

• V.I.D.E.O.s IS AN EFFICIENT TOOL OF SOCIAL

MANIPULATION OF LARGE GROUPS OF POPULATION

AND GENERATING BILLIONS IN PROFIT

• ALL THE PANDEMICS OF THE 20TH AND EARLY 21ST

CENTURY INCLUDING AIDS, LYME, AND SWINE FLU…

RESURRECTING PANDEMIC FLU OF 1918

• 1997 RELEASE OF UPGRADED AVIAN H5N1 FLU :

• NEW NS1 FOUR AMINO ACID DELETION BYPASSING

IL4 IMMUNE ALARM,

• OLD 1918 PB2 AND OTHER LETHAL GENETIC SNPs

FROM 1918 WNS33 HUMAN / IOWA 1930 PIG FLU

RECOMBINANT VIA TYPHUS PASS-THROUGH

COMINGLING OF VIRUSES IN PIGS

• H GENE 6 BASIC AMINO ACIDS CHANGE FROM 1971

U OF EDIBURGH, SCOTLAND H5N1 FLU WHO

REFERENCE LAB SEQUENCES

• ONLY 3 OF 5 AMINO ACIDS IN RECEPTOR BINDING

DOMAIN TO ATTACH TO HUMAN CELLS ON H GENE

• A H1N1 MEXICAN LABVIRUS HAS ALL FIVE

RECEPTOR BINDING H GENES, 2.3 TIMES FASTER

TRIMER OF PB1, PB2 AND PA GENETIC REPLICATION

CDC A H1N1 MEXICAL FLU

ELECTRON MICROSCOPY

A H1N1 TRIPLE TRIPLE

LABVIRUS RECOMBINANT

A H1N1 SWINE MEDICANN FRANKENVIRUS

FOUR SOURCES & THREE CONTINENTS

6 TO 8 % NO DATABASE GENE MATCHES

DR ADRIAN GIBBS PhD VIRAL GENETICS

LAB RECOMBINANT ORIGINS

LAB ORIGINS OF A H1N1

PANDEMIC SWINE FLU

Resurrected Pandemic Influenza Viruses∗

• Terrence M. Tumpey and Jessica A.

Belser

• Influenza Division, National Center for

Immunization and Respiratory Diseases,

Centers

• for Disease Control and Prevention,

Atlanta, Georgia 30333; email:

[email protected]

PLASMID ENGINEERED FLU VIRUSES


• Abstract• Influenza viruses continue to pose a major global public health problem.

• There is a need to better understand the pathogenicity and transmission

• of pandemic influenza viruses so that we may develop improved methods

• for their prevention and control. Reconstruction of the 1918 virus

• and studies elucidating the exceptional virulence and transmissibility of

• the virus are providing exciting new insights into this devastating pandemic

• strain. The primary approach has been to reconstruct and analyze

• recombinant viruses, in which genes of the 1918 virus are replaced with

• genes of contemporary influenza viruses of lesser virulence. This review

• highlights the current status of the field and discusses the molecular determinants

• of the 1918 pandemic virus that may have contributed to

• its virulence and spread. Identifying the exact genes responsible for the

• high virulence of the 1918 virus will be an important step toward understanding

• virulent influenza strains and will allow the world to better

• prepare for and respond to future influenza pandemics.


• The high replication efficiency of the reconstructed

1918 virus observed in mouse and human airway cells appears to

be the result of molecular determinants in the HA, NA, and PB1

virus genes.

• The role of PB1 may reflect the polymerase activity of the PB1

protein itself or the proapoptotic viral protein, PB1-F2, generated

by an alternative reading frame in the PB1 gene segment.

• While the role of the PB1 gene is likely to be crucial component of

1918 virus virulence, PB2 appears to contribute to the

transmissibility of this virus by allowing increased replication at

lower temperatures in the airways of mammals.

• Although a number of selected 1918 virus genes were critical, it is

most certainly the coordinated expression of all 1918 virus genes

that confers the unique highly virulent, transmissible phenotype

observed with this pandemic virus.

Resurrected Pandemic Influenza Viruses∗• 1. Sequence analysis of the 1918H1N1viral

genome and the plasmid-based reverse genetics

system has allowed researchers an

unprecedented opportunity to study the

composition of the virus responsible for the

influenza pandemic of 1918.

• 2. Among the eight 1918 gene segments studied,

the HA, NA, and PB1 genes contributed

significantly to the efficient replication and

enhanced virulence of the pandemic strain.

• 3. The surface glycoproteins and PB2 segments

of the 1918 virus are sufficient to confer virus

transmissibility of an avian H1N1 virus.

Top Cited Literature by Dr Tumpey & Belser

• Demonstrated that viruses possessing the

1918 NS gene segment were attenuated in mice.

• 7. Basler CF, Reid AH, Dybing JK, Janczewski TA,

Fanning TG, et al. 2001. Sequence of the 1918 pandemic

influenza virus nonstructural gene (NS) segment and

characterization of recombinant viruses bearing the

1918 NS genes. Proc. Natl. Acad. Sci. USA 98:2746–51

• Identified that glycan topology, as well as glycan

composition, affects receptor binding of influenza

viruses.

• 11. Chandrasekaran A, Srinivasan A, Raman R,

Viswanathan K, Raguram S, et al. 2008. Glycan topology

determines human adaptation of avian H5N1 virus

hemagglutinin. Nat. Biotechnol. 26:107–13


• Documents the discovery of PB1-F2 protein, generated

by an alternative reading frame of the influenza PB1

gene.

• 13. Chen W, Calvo PA, Malide D, Gibbs J, Schubert U, et

al. 2001. A novel influenza A virus mitochondrial protein

that induces cell death. Nat. Med. 7:1306–12

• Describes the plasmid-based reverse genetics system

used to rescue influenza A viruses in cell culture.

• 21. Fodor E, Devenish L, Engelhardt OG, Palese P,

Brownlee GG, Garcia-Sastre A. 1999. Rescue of

influenza A virus from recombinant DNA. J. Virol.

73:9679–82


• Testing of singlegene H1N1 reassortant 1918 viruses

identified crucial role of HA, NA, and PB1 segments in

virus replication and virulence.

• 74. Pappas C, Aguilar PV, Basler CF, Solorzano A, Zeng

H, et al. 2008. Single gene reassortants identify a critical

role for PB1, HA, and NA in the high virulence of the

1918 pandemic influenza virus. Proc. Natl. Acad. Sci.

USA 105:3064–69

• Reported the first documented influenza outbreak caused by a

wholly avian virus directly transmitting to humans from

infected poultry and causing death.

• 94. Subbarao K, Klimov A, Katz J, Regnery H, Lim W, et al.

1998. Characterization of an avian Influenza A (H5N1) virus

isolated from a child with a fatal respiratory illness. Science

279:393–96


• Describes the initial isolation and phylogenetic analysis

of multiple genes of 1918 virus sequences, which are

consistent with an H1N1 influenza A virus belonging to

the subgroup of strains that infects humans.

• 98. Taubenberger JK, Reid AH, Krafft AE, Bijwaard KE,

Fanning TG. 1997. Initial genetic characterization of the

1918 “Spanish” influenza virus. Science 275:1793–96

• First report characterizing the fully reconstructed 1918

virus, including mammalian challenge data.

• 103. Tumpey TM, Basler CF, Aguilar PV, Zeng H,

Solorzano A, et al. 2005. Characterization of the

reconstructed 1918 Spanish influenza pandemic virus.

Science 310:77–80

REVERSE ENGINEERED FLU

PLAGUES & THERAPEUTICS

WORLD DEPOPULATION IS TOP

NSA AGENDA - CLUB OF ROME• National Security Council's Ad Hoc Group on

Population Policy.

• Policy-planning group is in the U.S.State

Department's Office of Population Affairs,

established in 1975 by Henry Kissinger, State

Department's Office of Population Affairs

(OPA).

• This group drafted the Carter administration's

Global 2000 document

• National Security Study Memorandum 200"

(NSSM 200)... "food as a weapon“ Kissinger


NSA AGENDA - CLUB OF ROME

• The sphere of Kissinger In 1975, OPA

was brought under a reorganized State

Department Bureau of Oceans,

International Environmental, and Scientific

Affairs-- a body created by

Henry Kissinger.

• The agency was assigned to carry out the

directives of the NSC Ad Hoc Group.



• Kissinger initiated both groups after discussion

with leaders of the Club of Rome during the 1974

population conferences in Bucharest and Rome.

• The Club of Rome, controlled by Europe's black

nobility, is the primary promotion agency for the

genocidal reduction of world population levels.

• The Ad Hoc Group was given "high priority" by

the Carter administration, through the intervention

of National Security Adviser Zbigniew Brzezinski

and Secretaries of State Cyrus Vance and

Edmund Muskie.



• Bureau of Oceans, International

Environmental, and Scientific Affairs has

consistently blocked industrialization

policies in the Third World,

• Denying developing nations access to

nuclear energy technology--the policies

that would enable countries to sustain a

growing population.

NEW LAWS AND PLANS FOR THE

PERFECT PANDEMIC FLU STORM

• Public Readiness and Emergency Preparedness

Act 0f 2006.

• US government is using laws designed for dealing

with a very deadly pandemic, or bioterrorism, to

bring about a mass vaccination program for swine

flu

• This law removes liability from the manufacturer,

medical practitioners who use the product, and

from "government program planners" who decided

on using the law

NATIONAL GOVT TO WHO UN

PANDEMIC FLU CONTROL • MODEL STATE EMERGENCY HEALTH POWERS ACTS

• NATIONAL SECURITY PRESIDENTIAL DIRECTIVE/NSPD 51

and

• HOMELAND SECURITY PRESIDENTIAL DIRECTIVE/HSPD-20

• National Emergency Act – SEIZURE OF TRANSPORT,

PROPERTY, FOOD, ETC.

• PANDEMIC LEVEL 6 TRANSFER ALL CONTROL TO WHO UN

CONTROL – 2005 S.P.P. SECURITY AND SECURITY &

PROSPERITY PARTNERSHIP AND

• 2006 SIGNED194 NATIONS NEW UN WHO TREATY OF

PANDEMIC CONTROL BY WHO AND UN AUTHORITIES

• HHS HEALTH AND HUMAN SERVICES – OBAMA ADMIN – HHS

SEC. SEBELIUS – MANDATORY “VOLUNTARY WITH

CONSEQUEN CES” NATIONAL VACCINE FALL 2009 WINTER

2010



• Tamiflu and Relenza protection from

liability – Tamiflu Hallucinogenic “Angel

Dust”

• Novel Vaccine Adjuvants MF 59 Novartis,

and AS03 Glaxo Smith Kline – Squalene

oil based super adjuvants and Tween +

gp120 glycoprotein amplifier ( adjuvants

will be used in vaccines to stretch the

supply)



• Novartis began testing in humans in July, 2009

• Sanofi-Aventis and Glaxo Smith Kline in August

,2009

• Attenuated viruses WITHOUT adjuvant toxoins

• HHS is lobbying FDA to approve dangerous

protein antigen sparing adjuvants and vaccine

grown on non-egg cell lines from aborted baby cell

lines with various viral oncogenic , mycoplasma,

and bacterial contaminants



• Congressional Research Service, on April 27, 2009, the

Food and Drug Administration issued four Emergency Use

Authorizations (enacted in Section 564 of the Federal Food,

Drug, and Cosmetic Act, amended by the Project BioShield

Act of 2004) in response to requests from the CDC to make

available certain drugs (Tamiflu and Relenza), diagnostic

tests and respiratory protection devices.

• Use of unapproved (unlicensed) medical treatments and

tests, or use of approved treatments for unapproved uses

• Pregnant mothers Class 3 Dangers (4x risk

of H1N1 Flu Complications, Young adults

and children Unethical Testing Protocol

https://biotech.law.lsu.edu/blaw/H1N1-2009/R40560_20090521.pdf

https://www.cdc.gov/h1n1flu/eua/qa.htm

https://www.cdc.gov/h1n1flu/eua/qa.htm

https://www.fda.gov/OHRMS/DOCKETS/98fr/E9-8922.htm







• Vaccines containing MF59 and ASO3 have not

had Emergency Use Authorizations issued for

them--yet.

• USA government has purchased $698 million

dollars' worth of these adjuvants in August, 2009

• US and WHO officials have announced intentions

to use these viral antigen stretching adjuvants to

supply adequate vaccine for Fall 2009 – Winter

2010

https://www.bloomberg.com/apps/news?pid=20601085&sid=aeKFOHbajydM

THE PANDEMIC FLU MANIPULATED

PERFECT STORM

• New Bioterrorism laws (passed with the

expectation of use for much more dangerous

epidemics than the current swine flu)

• Allow use of untested products AND

• Give manufacturers an incentive to avoid

comprehensive testing (to avoid being found guilty

of willful misconduct) have

• Combined with the political imperative to provide

citizens with vaccines in a hurry,

• Yielding a potential Perfect Storm.

• SOURCE: Dr Meryl Nass MD MPH Int Med

1976 Swine Flu Vaccine Program

• 45 million people were vaccinated with an

inadequately tested vaccine

• Government gave the vaccine

manufacturers immunity from liability

• Created an alternative compensation

program

• Five thousand people sought benefits for

vaccine injuries

• 475 Guillain-Barre Syndrome

• Over 30 to 50 died directly from vaccine

TESTING AND SURVEILLANCE

OF A H1N1 FLU VACCINES

• Absence of Prelicensure Clinical Trial Data

• Mandatory Vaccination of All of US population will

cause death, spontaneous miscarriage,

autoimmune disease and progressive neurological

disorders and more…

• Road blocks and school lockdowns of „Voluntary

with Consequences‟ vaccination with refusal met

by forced quarantine with RFID steel bracelets

• Legal Injunctions in all states, countries, and

• Danger of violent resistance is very probable

Guillaine-Barre Paralysis Risk of A

H1N1 Flu Vaccination• The British Neurological Surveillance Unit

(BNSU), part of the British Association of

• Neurologists, has been asked to monitor closely

any cases of GBS as the vaccine is rolled out.

• One senior neurologist said last night: „I would not

have the swine flu jab because of the GBS risk.‟

• There are concerns that there could be a repeat of

what became known as the „1976 debacle‟ in the

US, where a swine flu vaccine killed 25 people –

more than the virus itself.

Guillaine-Barre Paralysis Risk of A

H1N1 Flu Vaccination• Australian National Medical Malpractice Insurance

will not insure doctors against suits for

complications such as GBS, death, or other

complications

• CMPA Canadian Medical Protective Association

will likewise be pressured into not protecting

doctors and nurses who participate in the National

Mandatory Vaccination Program

• US Private Medical Malpractice Insurers can also

be pressured into non-coverage for liability of

death, paralysis and autoimmune diseases and

other complications e.g. autism, miscarriage etc.

DEADLY 'SIX' CONSEQUENCES OF FORCED

MEXICAN A H1N1 VACCINATION PROGRAMS:

•

1] DEPRESSION OF IMMUNE PROTECTION AGAINST

ANY INFECTION AND MORE AND MORE SERIOUS

HUMAN CASES OF A H1N1 WITH HIGHER CASE

FATALITIES

2] ACUTE OR CHRONIC ADJUVANT TOXIN INDUCED

NEUROLOGICAL AND AUTOIMMUNE DISEASES OR

ACUTE SYSTEMIC COLLAPSE AND DEATH !-- CNS

DAMAGE, BEHAVIORAL DISORDERS, MOOD

DISORDERS, DEMENTIA, NEUROPATHY AND CNS

INDUCED DEATH !

3] STEALTH PATHOGENS IN HOT BATCHES E.G.

MYCOPLASMA, VIRUSES, FUNGI AND ACUTE OR

CHRONIC ILLNESS ... AUTOIMMUNE AND CANCER

DEADLY 'SIX' CONSEQUENCES OF FORCED

MEXICAN A H1N1 VACCINATION PROGRAMS:

• 4] RNA AND DNA PLASMA ANTIGENIC AMPLIFICATION

IN NEW TEST VACCINES CAN SWITCH ON GENES

CAUSING SERIOUS IMMEDIATE HEALTH DANGERS,

AUTOIMMUNE DISEASES AND CANCER INDUCTION

5] FASTER VIRAL GENETIC JUMPS TO MORE

PATHOGENIC SUBSTRAINS UNDER DRUG AND

GENETICALLY ATTENTUATED FULL OR PARTIAL

VIRAL GENOME IN NEW TEST VACCINES...

6] NAIS TRACKING BRACELETS OR INJECTED RFID

TRACKING CHIPS AS PART OF VERIFICATION OF

IDENTITY WITH BIOMETRIC CENTRAL DATABASES TO

VERIFY SAFE LICENSED TRAVEL IN THE USA AND

COUNTRIES WORLDWIDE !-- PART OF WHO UN

WORLD PANDEMIC CONTROL MATRIXX...!!

NO H1N1 PANDEMIC 6 JUSTIFIED UNLESS

VACCINES UPGRADE PATHOGENICITY• 1. The feared "2nd wave" of mutated "novel H1N1/H3N2/H5N1

RECOMBINANT PANDEMIC VIRUS" has not appeared!

• 2. The "flu season" in the Southern Hemisphere is winding down.

• 3. Studies concluded by the CDC have CLEARLY SHOWN that this

"lab-created" virus has average to low transmission issues

• 4. Yet, despite all of these facts, the WHO has not lowered the "Level

6" alert down to what is a much more appropriate Level 3 or 4. Why is

thiis? Simply because it is only at "Level 6" that the WHO has control

over the highly profitable MASS VACCINATION CAMPAIGN and

forcing cumpulsory vaccines in the 194 treaty nations.

Given these facts, it should be obvious that the "Pandemic" will not

happen, unless and until ATTENUTATED, LIVE VIRUSES are

systematically spread throughout the world via the VACCINE

NEEDLES, or MED-IMMUNE NASAL SPRAYS to young children.

•

Sept 1st 2009 NutriMedical Report Show, Dr True Ott PhD ND

NOVARTIS SPLIT VIRUS TH1

ADJUVANT TECHNOLOGY PATENT

NOVARTIS SPLIT VIRUS TH1

ADJUVANT TECHNOLOGY PATENT• 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.

• 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.

PANDEMRIX BIRD FLU VACCINE

• Europe GlaxoSmithKline's (GSK)

PANDEMRIX vaccine.

• This EMEA Document is very, very

revealing.

• The vaccine consists of: Active

Substance: Pandemic influenza vaccine

(H5N1) (split virion, inactivated,

adjuvanted) A/VietNam/1194/2004 NIBRG-

14.

• Clearly, this is BIRD FLU vaccine

Pandemrix European H5N1 Spit

Virion Pandemic Vaccine !?• Injecting millions of people with

PANDREMIX "adjuvanted" H5N1 Bird Flu

viruses could indeed create the 'Perfect

Storm'

• A H1N1 recombination with plasmids in

Europe‟s Pandemrix H5N1 Split Virion

would produce new viral index clade

branches with much higher case fatalities,

and rapid human to human spread

• Second wave A H1N1 lethal pandemic

wave may arise by this process

NOVARTIS 2005 PATENT FOR

H1N1 NOVEL FLU VACCINE • 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 allow

influenza viruses with desired genome

segments to be prepared in vitro using

plasmids

NOVARTIS 2005 PATENT FOR

H1N1 NOVEL FLU VACCINE • “African green monkey kidney cells” will be

used for the “viral growth substrate” – i.e.

the carrier medium. (Page 3, paragraph

0037)

• “oil-in-water” squalene-based adjuvants

will also be included (page 8 – 0098)

“recombinant” and “novel” split vaccine,

include fragments of attenuated viruses

(i.e. live pathogens) in the vaccine

medium. – Source: Dr True Ott PhD ND

OPERATION BIOSHIELD

REVERSE VIRAL ENGINEERING• CREATE FUTURE PATHOGENS AND

BIOWEAPONS TO INVENT

COUNTERMEASURES

• DayCart latest version of ProMis Oracle 8i

predictive software to plan

• Bioengineered Future Pathogens &

Bioweapons

• Develop Vaccines and Pharmaceuticals to

block pathogens

• Invent the problem and profit from the

solution

INTERNATIONAL SWINE FLU CONFERENCE

Washington, D.C., AUGUST 19TH TO 20TH 2009

• Top Five Reasons to Attend the Summit

• Gain a broad bird‟s eye view of the global swine

flu situation.

• Get the freshest updates from hard-to-reach

country experts.

• Learn how your company / organization can

prepare for a pandemic.

• Establish contacts with key local, federal and

international agencies involved in the fight against

swine flu.

• Draw on first hand best practices from top

companies to create solid business continuity

plans.

JURISDICTIONARY LEGAL MILITIA : INJUNCTION AGAINST

MANDATORY “VOLUTARY WITH DETENTION” A H1N1 VACCINES

• Injunctions are orders of a court of competent

jurisdiction commanding an individual,

business entity, or government agency to do

or stop doing something.

• Injunctions invoke what is called the equitable

powers of the court and, as such, those

seeking an injunction must come to court with

„clean hands‟.

• The party bringing such an action is called the

petitioner (not plaintiff). The party against

whom the action is brought is called the

respondent (not defendant).



• Injunctions are commenced by filing a petition

with a court of competent jurisdiction (could

be state or federal), effective service of a

summons „1‟ and copy of the petition on the

respondent(s) by an authorized process server

„2‟

• The elements that must be (1) alleged in the

petition and subsequently (2) proven by the

greater weight of admissible evidence through

the use of discovery are: , and payment of

required court fees.

LEGAL VACCINE

INJUNCTION

FIVE ELEMENTS

Threatened Harm

to the Petitioner

Outweighs Public

Interest

Threatened Harm

to the

Petitioner Outweighs

Harm to Respondent

Imminent Likelihood

of Irreparable Harm

Unavailability Of

any Adequate

Remedy at Law

Substantial Likelihood

of Success

Based on the

Allegations

YOU WIN !!



• 1. Existence of an imminent likelihood of irreparable

harm if the injunction is not issued,

• 2. Unavailability of any adequate remedy at law (i.e., an

award of money damages after the harm has occurred

will not restore the petitioner?s threatened loss,

• 3. The threatened harm to the petitioner outweighs any

substantial harm to the respondent,

• 4. Granting the injunction will not contravene a

substantial public interest, and

• 5. Petitioner has a substantial likelihood of success

based on the allegations, i.e., the facts alleged are likely

to be proven and are not merely speculative.

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• Note: In the aforementioned

„essential elements‟ that must be

• (1) alleged and (2) proven by the

greater weight of admissible

evidence, each word has a

particular technical meaning that

will be used by the court to read

the petition.



• Note also: You need only allege those ultimate facts

that, if proven, establish all the five elements. Fail to

allege sufficient facts to establish all five, and your

petition will be dismissed for failure to state a claim on

which the court can grant relief (in some courts called a

cause of action). Allege too many facts, and you weaken

your case by muddying the waters beyond what is

necessary.

• Note this, too: You must be able to prove all the facts

you allege, so you will surely shoot yourself in the foot

if you allege innuendo, assumptions, wild accusations,

etc. Stick to those facts that, if proven, will suffice to

establish all five elements.

• That‟s how you win!

•

1 2 3 4

Due Process Is the KING of ALL RIGHTS

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