LAB ORIGINS OF A H1N1 MEXICAN FRANKENFLU

1
LAB ORIGINS OF A H1N1 MEXICAN FRANKENFLU
TOXIC EUGENIC MANDATORY VACCINES

• DR BILL DEAGLE MD DABFP AAEM A4M
• NUTRIMEDICAL.COM LABVIRUS.COM BLOG

2
TIMETHEH
Introduction
1
ORIGINS OF PANDEMIC FLU
Strategy
WHO UN EUGENICS
POPULATION CONTROL
2
Challenges Forward

RESCUE FROM PANDEMIC FLU TOXIC VACCINES
3
3
1918 H1N1 SWINE FLU
VACCINE MISHAP EUGENIC BIOWEAPONS
H5N1 AVIAN FLU 1997
A H1N1 LABFLU 2009
4
LAB ORIGINS OF A H1N1SWINE FLU
5
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

6
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

7
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

8
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

9
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

10
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

11
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

12
CDC A H1N1 MEXICAL FLU ELECTRON MICROSCOPY
13
A H1N1 TRIPLE TRIPLE LABVIRUS RECOMBINANT
14
A H1N1 SWINE MEDICANN FRANKENVIRUS ? FOUR
SOURCES THREE CONTINENTS ? 6 TO 8 NO
DATABASE GENE MATCHES
15
DR ADRIAN GIBBS PhD VIRAL GENETICS ? LAB
RECOMBINANT ORIGINS
16
LAB ORIGINS OF A H1N1 PANDEMIC SWINE FLU
17
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 tft9_at_cdc.gov

18
PLASMID ENGINEERED FLU VIRUSES
19
Resurrected Pandemic Influenza 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.

20
Resurrected Pandemic Influenza Viruses

• 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.

21
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.

22
Top Cited Literature by Dr Tumpey Belser

• Demonstrated that viruses possessing the1918 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 98274651
• 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.
  2610713

23
Top Cited Literature by Dr Tumpey Belser

• 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. 7130612
• 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.
  73967982

24
Top Cited Literature by Dr Tumpey Belser

• 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 105306469
• 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
  27939396

25
Top Cited Literature by Dr Tumpey Belser

• 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 275179396
• 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 3107780

26
REVERSE ENGINEERED FLU PLAGUES THERAPEUTICS
27
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

28
WORLD DEPOPULATION IS TOP 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.  

29
WORLD DEPOPULATION IS TOP NSA AGENDA - CLUB OF
ROME

• 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.

30
WORLD DEPOPULATION IS TOP NSA AGENDA - CLUB OF
ROME

• 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.

31
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

32
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

33
NEW LAWS AND PLANS FOR THE PERFECT PANDEMIC FLU
STORM

• 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)

34
NEW LAWS AND PLANS FOR THE PERFECT PANDEMIC FLU
STORM

• 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

35
NEW LAWS AND PLANS FOR THE PERFECT PANDEMIC FLU
STORM

• 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

36
NEW LAWS AND PLANS FOR THE PERFECT PANDEMIC FLU
STORM

• 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

37
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

38
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

39
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

40
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.

41
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.

42
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 FATALITIES2 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

43
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 INDUCTION5 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...!!

44
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

45
NOVARTIS SPLIT VIRUS TH1 ADJUVANT TECHNOLOGY
PATENT
46
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. 

47
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

48
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 Europes
  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

49
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

50
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

51
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

52
INTERNATIONAL SWINE FLU CONFERENCE Washington,
D.C., AUGUST 19TH TO 20TH 2009

• Top Five Reasons to Attend the Summit
• Gain a broad birds 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.

53
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).

54
JURISDICTIONARY LEGAL MILITIA INJUNCTION
AGAINST MANDATORY VOLUTARY WITH DETENTION A
H1N1 VACCINES

• 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.

55
Threatened Harm to the Petitioner
Outweighs Harm to Respondent
Unavailability Of any Adequate Remedy at Law
Threatened Harm to the Petitioner Outweighs
Public Interest
LEGAL VACCINE INJUNCTION FIVE ELEMENTS
Imminent Likelihood of Irreparable Harm
Substantial Likelihood of Success Based on the
Allegations
YOU WIN !!
56
JURISDICTIONARY LEGAL MILITIA INJUNCTION
AGAINST MANDATORY VOLUTARY WITH DETENTION A
H1N1 VACCINES

• 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.

57
JurisDictionary Legal Militia Start or Join a
Chapter in Your Town, City, State or Country

• Go to www.NutriMedical.com or www.CLAYandIRON.com
  and Click on Products by Company? Down to
  JurisDictionary and Online or the JurisDictionary
  Legal Militia Educational Library
• OR Phone 866-Law-EASY and Talk to Dr Fred Graves
  J.D. or his staffThey are one of our great
  sponsorsSay to them that you were sent to join
  the Legal Militia by Dr Bill Deagle MD The
  NutriMedical Report and CLAYandIRON SHOW

58
JURISDICTIONARY LEGAL MILITIA INJUNCTION
AGAINST MANDATORY VOLUTARY WITH DETENTION A
H1N1 VACCINES

• 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.

59
JURISDICTIONARY LEGAL MILITIA INJUNCTION
AGAINST MANDATORY VOLUTARY WITH DETENTION A
H1N1 VACCINES

• 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.
• Thats how you win!

60
Due Process Is the KING of ALL RIGHTS
61
Thank You! Dr Bill Deagle MD
www.NutriMedical.com www.CLAYandIRON.com www.LabVi
rus.com BLOG