Nov 15, 2013 by DAVE MIHALOVIC
The Office of the Gene Technology Regulator (OGTR) is on its way to
approve a licence application from PaxVax Australia (PaxVax) for the
intentional release of a GMO vaccine consisting of live bacteria
into the environment in Queensland, South Australia, Western Australia
and Victoria.
According to the regulator, it qualifies as a limited and controlled release under section 50A of the Gene Technology Act 2000 (the Act).
PaxVax is seeking approval to conduct the clinical trial of
a genetically modified live bacterial vaccine against cholera. Once
underway the trial is expected to be completed within one year, with
trial sites selected from local government areas (LGAs) in Queensland,
South Australia, Victoria and Western Australia. PaxVax has proposed a
number of control measures they say will restrict the spread and
persistence of the GM vaccine and its introduced genetic material,
however there is always a possiblity of these restrictions failing and
infecting wildlife and ecosystems.
Aerial vaccines have used in the United States directed towards
animals by the use of plastic packets dropped by planes or helicopters.
Sanofi (who is one of the largest vaccine manufacturers in the world) has subsidiary companies such as Merial Limited who manufacture Raboral, an oral live-virus poisonous to humans yet distributed wildlife in the masses.
WEST NILE VIRUS SPRAYING
In 2006 Michael Greenwood wrote an article for the Yale School of
Public Health entitled, "Aerial Spraying Effectively Reduces Incidence
of West Nile Virus (WNV) in Humans." The article stated that the
incidence of human West Nile virus cases can be significantly reduced
through large scale aerial spraying that targets adult mosquitoes,
according to research by the Yale School of Public Health and the
California Department of Public Health.
Under the mandate for aerial spraying for specific vectors that pose a
threat to human health, aerial vaccines known as DNA Vaccine
Enhancements and Recombinant Vaccine against WNV may be tested or used
to "protect" the people from vector infection exposures. DNA vaccine
enhancements specifically use Epstein-Barr viral capside's with multi
human complement class II activators to neutralize antibodies. The
recombinant vaccines against WNV use Rabbit Beta-globulin or the poly
(A) signal of the SV40 virus. In early studies of DNA vaccines it was
found that the negative result studies would go into the category of
future developmental research projects in gene therapy. During the
studies of poly (A) signaling of the SV40 for WNV vaccines, it was
observed that WNV will lie dormant in individuals who were exposed to
chicken pox, thus upon exposure to WNV aerial vaccines the potential
for the release of chicken pox virus would cause a greater risk to
having adult onset Shingles.
CALIFORNIA AERIAL SPRAYING for WNV and SV40
In February 2009 to present date, aerial spraying for the WNV
occurred in major cities within the State of California. During
spraying of Anaheim, CA a Caucasian female (age 50) was exposed to
heavy spraying, while doing her daily exercise of walking several
miles. Heavy helicopter activity occurred for several days in this
area. After spraying, she experienced light headedness, nausea, muscle
aches and increased low back pain. She was evaluated for
toxicological mechanisms that were associated with pesticide exposure
due to aerial spraying utilizing advanced biological monitoring
testing. The test results which included protein band testing
utilizing Protein Coupled Response (PCR) methods were positive for
KD-45. KD-45 is the protein band for SV-40 Simian Green Monkey virus.
Additional tests were performed for Epstein-Barr virus capside and
Cytomeglia virus which are used in bioengineering for gene delivery
systems through viral protein envelope and adenoviral protein envelope
technology. The individual was positive for both; indicating a highly
probable exposure to a DNA vaccination delivery system through nasal
inhalation.
Pentagon Document Revealed Aerial Vaccination Plans
In the Quarterly FunVax Review in June, 2007,
the report lists the objective of a project listed as ID: 149AZ2 as a
preparation of a viral vector that will inhibit/decrease the
expression of a specific disruption gene (VMAT2) within a human
population. It further indicates in the abstract that six method of
virus dispersal were tested including high altitude release, water
supply release, insect transmission, and various methods of diffusion.
Sources:
ogtr.gov.au
vactruth.com
cdc.gov
Dave Mihalovic is a Naturopathic Doctor who specializes in vaccine research, cancer prevention and a natural approach to treatment.
http://preventdisease.com/news/13/111513_Australia-Determined-To-Forcibly-Vaccinate-By-Intentional-and-Controlled-Release-Aerosolized-GMO-Vaccine.shtml?utm_source=111513&utm_campaign=111513&utm_medium
DAY TO DAY OPINION & ANALYSIS OF THE ISSUES THAT PERTAIN TO OUR HEALTH AND WELL BEING
Monday, November 25, 2013
AUSTRALIA DETERMINED TO FORCIBLY VACCINATE BY INTENTIONAL AND CONTROLLED RELEASE OF AEROSOLIZED GMO VACCINE
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