People are so utterly blind, ignorant and conditioned. Everything is connected and there is no such thing as coincidences. This is all verifyable information and sh*t gets deep. Who stands to profit? Follow the money. But this just isnt about money. The primary Ebola strain being spread right now (as there are 2) was bioengineered by the US Department of Defense (via USAMRIID) & Tulane University with the knowledge/help from pharma/biotech giants such as Monsanto, Alnylam, Bristol-Myers Squibb, Merck, Pfizer and a much smaller pharma company based out of Canada called Tekmira. A known Ebola strain from Central-Africa was used as the base, and was bioengeneered to become a new hybrid respiratory illness (a combination of Ebola Virus & Lassa Hemorrhagic Fever, weaponized via Tulane University & USAMRIID at Fort Detrick) making it become a genetic variant of the original strain. This bioengineered hybrid allowed for airborne human-to-human transmission, an extended incubation period (to increase spread/threat), and a slightly toned down virility (to have the ideal initial wanted mortality rate (~40%)). Ebola (EBOV) – Human-to-human transmission occurs via direct contact with blood or bodily fluids from an infected person (including embalming of an infected dead person) or by contact with contaminated medical equipment, particularly needles and syringes. Lassa (LASV) – Inhalation of tiny particles of infective material (aerosol) is believed to be the most significant means of exposure. Ebola/Lassa (EBOV/LASV) – Human-to-human transmission occurs via direct contact with blood or bodily fluids AND/ORInhalation of tiny particles of infective material (aerosol) from an infected person (including embalming of an infected dead person) or by contact with contaminated medical equipment, particularly needles and syringes. Ebola Virus was chosen as the base virus for the hybrid due to its high mortality rate and other ideal bio-warfare properties. Filoviruses like Ebola have been of interest to the Pentagon since the late 1970s, mainly because Ebola and its fellow viruses have high mortality rates — in the current outbreak, roughly 60 percent to 72 percent of those who have contracted the disease have died — and its stable nature in aerosol make it attractive as a potential biological weapon. The Sierra Leone Ebola hybrid strain (EBOV/LASV, ~40% mortality rate) is shown to have a lower mortality rate then the Guinea Ebola strain (ZEBOV, ~75% mortality rate), but is shown to instead be MUCH more human-to-human transmittable, due to it being an airborne hybrid. Basically there are 2 strains going on at the same time (75% Mortality – Ebola-Zaire) & (40% Mortality, Ebola/Lassa, airborne)). Volume 20, Number 7—July 2014: Undiagnosed Acute Viral Febrile Illnesses, Sierra Leone PRNT results indicated that the infecting virus was most closely related to EBOV, except for 1 SUDV-reactive patient sample. This finding was unexpected because our assumption was that any ebolavirus would more likely be TAFV, the only species described in West Africa. Although the serum samples were able to neutralize EBOV only at a low level (1:40 dilution), it is possible that the virus is an EBOV genetic variant. July 31, 2014 Stats Guinea = 339/460 = ~73% mortality rate = ~5-9 day incubation = Ebola-Zaires (natural Ebola-Zaire) Sierra Leone = 233/533 = ~43% mortality rate = ~9-21 day incubation = Ebola/Lassa (bioengineered hybrid, airborne) Because of these tweaks, the current strain of Ebola we should be worried about is actually a “respiratory virus” unlike any other Ebola strains that were previously known (as it is a bioengineered/weaponized hybrid). Because the US knows this airborne strain is a respiratory virus (the one that will develop into the actual Pandemic), they needed to make some last minute adjustments to their emergency pandemic protocols, which were just refined on July 31, 2014 by Barack Obama to suite the needed definition in preparation for a WHO Pandemic Level 6 Declaration (down the line). April 4, 2003 – Executive Order — Revised List of Quarantinable Communicable Diseases (b) Severe Acute Respiratory Syndrome (SARS), which is a disease associated with fever and signs and symptoms of pneumonia or other respiratory illness, is transmitted from person to person predominantly by the aerosolized or droplet route, and, if spread in the population, would have severe public health consequences. VS (just revised by Obama)… July 31, 2014 – Executive Order — Revised List of Quarantinable Communicable Diseases “(b) Severe acute respiratory syndromes, which are diseases that are associated with fever and signs and symptoms of pneumonia or other respiratory illness, are capable of being transmitted from person to person, and that either are causing, or have the potential to cause, a pandemic, or, upon infection, are highly likely to cause mortality or serious morbidity if not properly controlled. This subsection does not apply to influenza.” This bioengineered “respiratory” variation of the Ebola virus (EBOV/LASV) was then released via the Kenema Government Hospital Lassa Diagnostic Laboratory (Soros / Gates Foundation) in Sierra Leone by USAMRIID/Tulane University earlier this year, which used unwitting Lassa Fever Program subjects as hosts (which were made immune-carriers to the new hybrid virus they then unknowingly spread) as part of a Tulane University “Ebola testing” project being held in 3 regions of Africa (Sierra Leone, the Republic of Guinea, and Liberia). Manual of Security Sensitive Microbes and Toxins Security sensitive microbes (viruses, bacteria, fungi, and parasites) and toxins, which are often referred to as the select agents and toxins, have the capacity to cause serious illness and death in humans, animals, and plants. Throughout history, these microbes and toxins have been exploited in one form or another as biowarfare and bioterror agents that create fear and panic well beyond any actual physical damages they might cause. Basically when a WHO Pandemic Level 4 Emergency is declared, preparations for countermeasures would be started, which if escalated to a Pandemic Level 6 emergency, would then trigger implementation of mandatory (by law) mass vaccinations of the populous of even not effected areas/countries in what is deemed as “Pandemic Management” (aka the long awaited “phase 2″ that Baxter AG fu*ked up in 2009). WHO Pandemic Levels Level 4 = Prepare (preparation) A reassortant virus is causing community-level outbreaks, meaning there are sustained disease outbreaks in a community. This marks a “significant upwards shift in the risk for a pandemic.” However, a pandemic isn’t necessarily a forgone conclusion. Level 5 = Mobilize (initiation) There is human-to-human spread of the virus into at least two countries in one WHO region. Most countries aren’t affected at this stage, but declaration of Phase 5 is a “strong signal that a pandemic is imminent.” There is little time remaining to finish the organization, communication and implementation of the planned mitigation measures. Level 6 = Sustain (vaccination) In addition to the countries affected in Phase 5, there are community-level outbreaks in at least one other country in a different WHO region. A global pandemic is occurring. Just hope people see this event for what it is… and understand what is to come. The jist of the plan in 2009 was this… 2009 Swine Flu Pandemic Phase 1 (cover) 1. Release a fairly harmless human-to-human transmittable swine flu strain (H1N1) near the Mexico border. 2. Infect a small number of subjects in China with a non human-to-human transmittable strain of bird flu (H5N1). 3. Overlap both during a natural influenza season (H3N2). 4. Push the need for mass vaccinations by overly hyping the virility of the H1N1 strain being circulated (cause). Phase 2 (real pandemic) 5. As part of the vaccination program, infect various groups of subjects with a the real Pandemic, a bioengineered hybrid of all 3 (H1N1/H5N1/H3N2), which was to be included in a small percentage of the initial Baxter AG Swine-Flu Vaccine (this is the stage they got caught at just prior to launching and had to call it off, and recall the vaccines in question just prior to being used). The end result if everything went as planned would of been an airborne human-to-human transmittable hybrid virus (H1N1/H5N1/H3N2), with a ~10-14 day incubation period, and a ~40% mortality rate. Note: They required the 3 “natural strains (H1N1, H5N1, H3N2) to be active before releasing the weaponized hybrid (H1N1/H5N1/H3N2) so that the bioengineered hybrid once released could be written of as being “naturally created”. Because of this they had to regroup and tweak/simplify the framework slightly, so that the plan no longer relied on the mass vaccination stage in order to initiate the Phase 2 release… Which brings us to today… 2014 Ebola Epidemic/Pandemic Phase 1 (cover) 1. Release a standard Ebola-Zaire strain in Guinea. 2. Do it near an area that currently has Lassa active (Nigeria) so that a few weeks later the 2 viruses will overlap in at least 1 area. Note: Again this is done so that when they release the weaponized hybrid of the 2 (EBOV/LASV) they can say it is “natural created”. Phase 2 (real pandemic) 3. Release the real Pandemic using a hybrid Ebola/Lassa (EBOV/LASV), to several unwitting subjects inside the Kenema Government Hospital in Sierra Leone. The end result is an airborne human-to-human transmittable hybrid virus (EBOV/LASV), with a ~9-21 day incubation period, and a ~40% mortality rate. Meaning sh*ts not looking good even if you want t9 dismiss it like youve been trained to do.
Posted on: Mon, 13 Oct 2014 13:57:04 +0000
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