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Dr Deagle Show 021210 1/4 - DR GARY RIDENOUR MD & DR MAYER EISENSTEIN MD JD

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Uploaded by on Feb 13, 2010

http://www.nutrimedical.com/news.jhtml?method=view&news.id=2634

- - - THIS IS NOT AN OFFICIAL CHANNEL OF THE NUTRIMEDICAL REPORT OR DR. BILL DEAGLE - -

playlist: http://www.youtube.com/view_play_list?p=ED1F8770C49E74C0

NUTRIMEDICAL REPORT SHOW -- FRIDAY, FEBRUARY 12TH 2010 -- HOUR THREE SPECIAL -- WAVE 3 OF THE H1N1 FRANKENFLU EMERGES WITH D225G D225N H274Y AND NEW POLYMORPHISMS TO INCREASE CASE LETHALITY AND REDUCE TOTAL WORLD CASES AS THE PLAQUE ADVANCES -- DR GARY RIDENOUR MD & DR MAYER EISENSTEIN MD JD

SWINE FLU HYBRID AND BRIDGE VIRUS TO SWINE-AVIAN FLU PANDEMIC GENES



The swine flu is common in the agribusiness, and antibodies to swine flu are present in 20% of vetenarians and 5% of pig farm workes, and rarely kills pigs.

However, this swine flu that has presented in Mexico, Texas, California, Queens NYC, London, Italy, etc. has genes of swine, avian, human, and asian flu. This is without any doubt a pandemic flu with a current case fatality estimated at 10 % plus, and rapidly is leaping across North America and to Europe.

Since 1997, the H5N1 flu has spread to all continents. Genetics showed that six strains had high pathogenic case fatality rates in the range of 70% average from 25 % to 100 % case fatality rates in humans, with some clusters of human to human spread, with close physical contact. Defiencies in two amino acids needed to allow rapid attachment to human cells was found in all strains, but can be acquired by recombinants with H9N2 or H7N3 or H3N2 etc. endemic human stains that can also coinfect pigs, birds, agricultural animals, and animals in the wild. Until fall 2008, the avian flu did not optimally replicate unless it was at 106 degrees or higher, but now it has acquired the capacity to replicate easily at 98.6 Farhenheit. Drug resistance to Amantadine, Tamiflu also are the predominant strains.

The current swine flu is analagous to a early 20th century steamer trunk, with stickers showing the visited countries and coastal cities. It has stamps from Asia, North America, Avian, Swine and Human genetics. This is a "Lab Creation". Now, we must understand that this virus is behaving as if it is more lethal per case that usual flu, and can recombine in pigs, wild and domestic birds, and other animals and can thus acquire PB2 deletions, NS1 gene polymorphisms, and the polybasic six amino acids that allow it to grow in brain and CNS as well as any other target organ in human and animal hosts. The NS1 deletion of four amino acids bypasses IL4, and thus is much more lethal with massive cytokine release at end stages. Because Avian H5N1 and the 1918 Swine Flu targeted young healthy people, the release of cytokines was more violent in the most healthy. This first wave is likely to recombine and after Phase 1 gene to population insertion, Phase 2 will result in new superstrains with additional genetic polymorphisms allow transfer efficiently to humans. Phase 2 is the bioreactor phase. In the emergent or Phase 3, new viral Clades of Swine /Avian hybrids will then have more efficient spreading and higher spontaneous lethality.

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  • If they won't stop trying 2 kill us, we should at least:

    LAUGH with DEAD JFK

    As he examines 9-11

    watch?v=8DQp0QxkBCU

  • black people have been burnt too many times with vaccines (e.g. syphillis/tuskegee), etc. so no surprise they are hesitant...

  • 1st2view, thanks for posting. Dr. Deagle is good.

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