For immediate release
Contact: Eileen Dannemann, director ncowmail@gmail.com
917-804-0786
October 11,2005
PRESS RELEASE
AIDS and Avian Flu
Plagues, Made in America?
Researchers and scientists recommend
an emergency restraining order on
MedImmune Vaccines, Inc., FLU MIST
According to researcher team, Dr.
Mark and David Geier, the current flu vaccines
are not only ineffective against the expected
Avian Bird Flu pandemic but that “the FDA
Approved thimerosal/mercury-free FLU MIST
(MedImmune Vaccines, Inc., Gaithersburg, MD)
vaccine may create a super strain virus plague”,
warns Dr. Mark Geier.
The well respected research team has already alerted members of the
medical community in Washington,
DC recommending that any support for the FluMist
vaccine be withdrawn immediately and a
restraining order be issued to the vaccine
manufacturers. The immediate and present danger
lies in the suspicion that the FluMist contains
2 key genetic sequences needed for efficient
human-to-human transmission that the avian flu
is missing.
FluMist is a live cold-adapted trivalent nasally
administered vaccine, which is currently being
recommended for individuals between the age of 5
and 49 years. According to the 2005 Physicians
Desk Reference (PDR), the probability of
acquiring a transmitted vaccine virus following
close contact with a single FluMist inoculee was
estimated to be 2.4% (95% CI: 0.13-4.6) [31].
Because of the possible transmission of this
vaccine’s viruses, vaccine recipients are
advised to avoid close contact with immuno-compromised
individuals for at least 21 days. Additionally,
persons with conditions such as human
immunodeficiency virus infection, malignancy,
leukaemia, or lymphoma, and patients who may be
immunosuppressed or have altered or compromised
immune status as a consequence of treatment with
systemic corticosteroids, alkylating drugs,
antimetabolites, radiation, or other
immunosuppressive therapies, may be at
significant risk if exposed within 21 days to a
FluMist vaccine inoculee.
Other individuals who might be at high risk if
exposed within 21 days to FluMist inoculees,
include, but are not limited to, adults and
children with chronic disorders of the
cardiovascular and pulmonary systems, including
asthma
(which up to 25% of
today’s children seem to have);
pregnant women; and adults and children who
required regular medical follow-up or
hospitalization during the preceding year
because of chronic metabolic diseases (including
diabetes), renal dysfunction, or
hemoglobinopathies. Additionally, because
FluMist contains live influenza viruses, there
is the possibility with the widespread use of
FluMist,
that an individual might have a second
concurrent viral infection
with another influenza
strain(such as the avian
bird flu), with the possibility that the live
viruses from the FluMist recombine/re-assort
with the second viral infection to produce a
“super
virus.”
It is obvious from the extensive list of persons
who might be at risk if exposed to a FluMist
vaccine recipient within 21 days of vaccination,
along with potential ability of the live
influenza viruses within FluMist to
recombine/re-assort with other viruses, that the
continued use of FluMist presents a significant
potential danger to the health and well-being
of a wide segment of the population. This
raises major concerns about the wisdom and
ethics of recommending the use of FluMist for
use in the general population.
Etiology of the Avian bird flu
According to Dr.
Boyd Graves, who has been marginalized over the
years by “official” government medical
communities for speaking up about the
possibility that AIDS was purposefully designed
to be an ethnic specific virulent, genocidal
agent, Avian flu pandemic
could bescience run amuck.
“Amidst the current Centers for Disease Control
media orchestrated public panic over the Avian
Flu Pandemic, more and more scientists are
beginning to look at the appearance of these
lethal virulents as being
adapted by science,
genetically recombined as biowarfare agents,
made in America,”
says Graves.
The historical trail traces itself back to the 1843 discovery of
the infectious agent (MYCOPLASMA)
for the “SPOTTED LEAF
DISEASE”, also known as the “TOBACCO MOSAIC
VIRUS.”
“At the core of human (cancer) disease”, says
Graves, is this ‘mycoplasma’ entity that has
been weaponized over time realizing lethal and
incapacitating conditions for humanity”.
“The development of the mycoplasma from plant to animal to human is
clear”,
asserts
Graves.
“By 1898 the United States had realized the
mycoplasma in cows, bovine spongiform
encephalitis (BSE). By 1902, they had realized
it in horses, equine infectious anemia virua (EIAV),
in 1904, they realized it in goats, caprine
arthritic encephalitis virus (CAEV). By 1910,
they had realized it in fowl, Rous Sarcoma Virus
(RSV)”, reports Graves after years and years of
committed research into the subject.
According to page 14 – 15 of the 1978 progress report of the U.S.
Special Virus program, the 1910 RSV is a product
of recombinant genetics. Further review will
show the 1918 Spanish Flu was a recombinant bird
virus. “The same is true of the 2005 Avian flu’,
comments Graves.
Is “recombinant” a natural occurrence in Nature
or man made or both?
In 1918, the pandemic began not in a port city of this country, but
in the Midwest.
Tom Rogers, a whistleblower, working in the
field of virology in the
1990s
explains that the scientists who are “in the
know” look towards the mid west, in specific,
Missouri, to read the pulse of bird carrying
plagues.
“Birds from Asia and Europe converge at this
spot due to the convergence of the Mississippi,
Ohio and Missouri river. Various viruses
recombine organically”, says Rogers. Rogers
tells the story about the Missouri birthplace of
the USA born deadly Flu of 1918 claiming that it
was purposefully misnamed “Spanish Flu”
as a distraction. He tells how A.J.
Cohen, a veterinarian in Missouri in 1918 warned
meat packers and distributors that a super virus
was killing off pullets and piglets. However,
Cohen was not only disregarded but his life was
threatened by industry. “These meats were sent
throughout the nation and ultimately overseas”,
claims
Rogers.
American soldiers were exposed first to
the recombinant and their war travels spread the
virus to wherever they went. In fact, more
soldiers died from the Spanish Flu than those
who died in World War I. Rogers claim is that
there is no such thing as “jumping species” as
might have been designed and refined by
biotechnology techniques as claimed by Dr.
Boyd Graves and Dr. Leonard Horowitz, a popular
lecturer on the subject and author of AID, EBOLA
and other viruses. Rogers claims that the
virus passes amongst species due to “wrapping
your lips” around it, as he likes to phrase it.
As a result of his research into the etiology of
non specific species transferred plagues Rogers
is now a deeply committed Vegan…that is no meat,
no milk. He
says
the only way you can get the Avian Flu is by
“eating” the infected species,
or via fluid exchange, like blood transfers,
sex, and close saliva contacts,
like in AIDS.
Although one can usually find an originating template for bacteria,
viruses and drugs in nature, Dr.
Boyd Graves claims that US government
purposefully brought these lethal viruses to a
dangerous new level through biotechnology and
laboratory recombinant technologies
When the
United States began the Tuskegee syphilis
experiments in 1932, they also began the testing
of the infectious agent of HIV, the sheep virus
VISNA. HIV contains sequences from a 1932 strain of VISNA, strain ks1514.
However, in the 1971 progress report (#8) of the
U.S.
Special Virus program (1971), the United States
concedes that VISNA had not yet been associated
with human disease.
The United States
cannot explain how VISNA is the “etiological
agent” of HIV, as they report in 1985, 1986 and
1995. See, Science Vol 227, pp. 173 – 7,
January, 1985, see also, PROC NAS Vol 83, pp.4007 – 11, June 1986 and PROC NAS Vol 92, pp.
3283 – 87, April 11, 1995.
“I believe we can have a much better
understanding of medicine and science if we
review the U.S. Laboratory of Hygiene (circa
1878), the 1902 Cold Spring Harbor Laboratory,
the 1904 Station for Experimental Evolution and
the 1926 MIT 'Virus Cancer' Conference”, says
Graves. In addition, the May 1946
Appropriations Hearing addresses a "synthetic
biological agent" in "useable shape". “This is
the recognition of the VISNA agent, which now
wreaks havoc across the biomedical world”,
comments Graves. Dr. Boyd Graves is certain,
that if we review and investigate the U.S.
Special Virus program, we will solve not only
HIV and AIDS, but we will answer many of the
unknown origins of human disease.www.boydgraves.com
Meanwhile, Eileen Dannemann, director of the
National Coalition of Organized women
spearheading the collection of the various data
wonders if the US government has been recently
testing their virus collection on the greyhound
dogs…hence the new canine flu epidemic causing
CDC concerns about it “jumping species” and
infecting humans. Tom Rogers would say don’t
kiss your dog. Dr. Boyd Graves and Dr. Len
Horowitz would say…just another covert clinical
trial. Dr. Mark and David Geier would say, in
any case take Tamaflu, a prescriptive drug that
biomedically short circuits the progression of
flu disease. “Unfortunately",
Dannemann reports, a few young people in Japan
went crazy on Tamiful and committed acts of
bizzarre suicide as if they were on SSRI. But in any
case, I am a Vegan”, she winks as she dabs
biblical “essential oils” in her ears. Ms. Dannemann is developing a special anointing oil
that is a gift during times of
plagues... following the original biblical
formula. Coming soon:ProgressiveConvergence.com