WARNING! - H5N1 DNA in Flu Mist! - WARNING!
(CBS/The Early Show)
Researchers and scientists recommend an emergency restraining order on MedImmune Vaccines, Inc., FLU MIST ~ A MUST see VIDEO!
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alerted members of the medical community in Washington, DC recommending that any support for the FluMist vaccine be withdrawn immediately and a restraining order be issue to the vaccine manufacturers.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.
Flu Mist 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) . 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 a ethnic specific virulent, genocidal agent, Avian flu pandemic could be science 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 over seas”, 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 concludes, “Congress is so invested in spending millions of dollars stockpiling ineffective vaccines, there is no room at the CDC Inn for Tamaflu, a proven product that may save millions of lives. Perhaps the CDC doesn’t share patent royalties on Tamaflu”, she sighs. “But in any case, I am a Vegan”, she winks as she dabs biblical “essential oils” in her ears. www.ProgressiveConvergence.com
URGENT WARNING: H5N1 DNA in Flu Vaccine!
Dr. Leonard G. Horowitz - source www.vaclib.org/news/plagues.htm