EBOLA HOAX: Only First Few Cases Were Real - No Pictures from This Outbreak

Startling VRM Ebola Report by Joel Lord
~ Host Sallie O. Elkordy

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VRM: Ebola Report
20th October 2014 - By Joel Lord

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Another season of fear-mongering headlines & Government Health Department-spun pronouncements is upon us; our communities faced with a seemingly imminent (manufactured) health crisis being forced down our collective throats.

“As the (Ebola) epidemic gets more and more formidable and in some cases out of control it is quite conceivable, if not likely, that we may need to deploy the vaccine to the entire country to be able to shut the epidemic down. That is clearly a possibility.” U.S. National Institute for Allergy and Infectious Diseases (October 06, 2014)

The benchmark of sound journalism & good detective work in this field depends on the weight of scientific evidence presented, the accuracy of the data, and the ability to distinguish verifiable truth from (Pharmaceutical & Vaccine Industry) promulgated lies & misinformation – something clearly out of step with the Mainstream Media protocols of cover-up & deception.

We’ve been here before. History is predictably repeating itself…again.

Once again, as in 2009, the WHO are purposefully inflating the numbers of victims here, to ensure the maximum fear factor is felt throughout our communities. Until those clinics & hospitals impacted by this crisis release the actual (post mortem) laboratory results, any statistics being foisted on us represent nothing more than speculation at best.

‘These (Ebola) numbers are subject to change due to on-­going reclassification, retrospective investigation and availability of laboratory results…Work is also ongoing to resolve discrepancies between different sources of data, which may lead to a revision of the numbers of cases and deaths in the future.‘ WHO disclaimer

During the 2009 (CDC bio-laboratory produced) Pandemic. the WHO routinely exaggerated the overall death toll (attributable to H1N1); by including any/all cases associated with Flu-like symptoms – regardless of the fact that the VAST majority of victims ultimately died as a result of compromised immunity and/or pre-existing medical conditions. H1N1 was merely a blip on the radar, by all accounts a comparably mild seasonal flu.

Communities around the world were manipulated constantly by Mainstream Media outlets (in lock-step with the WHO & spineless Government health departments), via an ongoing barrage of misinformation, negative hype & fear-mongering propaganda. By the time all the dust settled it was unanimously determined by most experts in the scientific arena, “H1N1 has ultimately turned out to be, from a pandemic perspective, a dud.”

Therefore, It’s vitally important to analyze the current Ebola scare objectively.

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So what, exactly, are we dealing with here? Is this, indeed, a legitimate (naturally occurring) catastrophe of unprecedented proportions we see unfolding? Is the Ebola Virus that serious a threat vs. a manufactured crisis? Or are we being deceived by a multi-billion dollar Industry, beholden to the Military Industrial Complex, bent on establishing a universal 99% “herd immunity” policy – the precursor to an eventual Government lock-down on individual freedom to choose, the official implementation of mandatory vaccinations across the board?

The recent Ebola outbreak in Africa coincides with a massive Meningitis Vaccine campaign targeting “150 million Africans”, many throughout Guinea & Nigeria.

The low-budget vaccine, MenAfriVac®, (less than US$0.50 per dose) was “kept outside the cold chain for up to four days at up to 40°C”.

Neighboring Liberia & Sierra Leone, both primary epicenters, were recently subject to the “largest ever Yellow Fever Immunization Program” conducted in that region – an estimated 12 million locals impacted (infected) by the compound shot.

Why has the Ebola virus suddenly erupted in a region of Africa known as the “Meningitis Belt” (comprising all four countries affected – Guinea, Liberia, Nigeria & Sierra Leone)?

Because the WHO & CDC are deliberately trying to cover up their bloody tracks.

This supposed outbreak of Ebola bares all the hallmarks of a rarified, virulent strain of bacterial Meningitis, ‘Acute fulminating Meningococcal Septicemia’, also known as ‘Waterhouse-Friderichsen Syndrome’, a virulent form of bacterial meningitis marked by extreme vomiting, hemorrhaging – excessive bleeding around the eyes & mouth, severe blackish bruising on the arms & legs, leading to Septic shock and potentially even death. These acute symptoms closely resemble those seen in Ebola victims.

Could this be yet another case of a dangerous, untested vaccine triggering a tsunami of viral & bacterial mutations, in impoverished regions?

Waterhouse-Friderichsen Syndrome: ‘‘The prodromal symptoms were similar to those encountered in any respiratory infection, consisting of headache, chilly sensations, muscular pains and malaise. The onset of the bacteremia was sudden and dramatic. The most striking features were the profound shock and the petechial eruption, which in the course of a few hours became purpuric…This condition gradually progressed until numerous coarse, bubbling rales could be heard over both lung fields. With the appearance of frank pulmonary edema terminally, the patient lapsed into coma and died shortly thereafter.‘

Meningococcal Septicemia (Septic shock): ‘The hallmarks of severe sepsis and septic shock are changes that occur at the microvascular and cellular level with diffuse activation of inflammatory and coagulation cascades, vasodilation and vascular maldistribution, capillary endothelial leakage, and dysfunctional utilization of oxygen and nutrients at the cellular level. The challenge for clinicians is to recognize that this process is under way when it may not be clearly manifested in the vital signs or clinical examination.‘ Andre Kalil, MD, MPH Professor of Medicine, Department of Medicine, Section of Infectious Diseases; Director, Transplant ID Program, University of Nebraska Medical Center

Note: ‘DIC (Disseminated intravascular coagulation), is most commonly observed in severe sepsis and septic shock. Indeed, the development and severity of DIC correlate with mortality in severe sepsis. Although bacteremia, including both gram-positive and gram-negative organisms, is most commonly associated with DIC, other organisms (eg, viruses, fungi, and parasites) may also cause DIC.

DIC exists in both acute and chronic forms. Acute DIC develops when sudden exposure of blood to procoagulants (eg, tissue factor [TF], or tissue thromboplastin) generates intravascular coagulation. Compensatory hemostatic mechanisms are quickly overwhelmed, and, as a consequence, a severe consumptive coagulopathy leading to hemorrhage develops. Abnormalities of blood coagulation parameters are readily identified, and organ failure frequently results.‘ Marcel M Levi, MD Dean, Academic Medical Center, University of Amsterdam, The Netherlands

A Virus (such as Ebola) is defined as a microorganism, consisting of strands of RNA/DNA ‘smaller than a bacterium that cannot grow or reproduce apart from a living cell. A virus invades living cells and uses their chemical machinery to keep itself alive and to replicate itself. It may reproduce with fidelity or with errors (mutations); this ability to mutate is responsible for the ability of some viruses to change slightly in each infected person, making treatment difficult.‘

Notably, all viruses are distinguished by an inability to reproduce on their own. ‘They infect the cells of living organisms from plants to people, hijacking the host’s cellular machinery to reproduce itself.‘

Bacteria, on the other hand are defined as ‘single-celled microorganisms that differ from all other organisms (the eukaryotes) in lacking a true nucleus and organelles such as mitochondria, chloroplasts, and lysosomes. Their genetic material consists of a single loop of double-stranded DNA, whereas the genetic material of eukaryotes consists of multiple chromosomes, which are complex structures of DNA and protein.‘

Note: ‘Genetic material can be transferred between bacteria by three processes: transformation (absorption of naked DNA), transduction (transfer by a virus), and conjugation (transfer by independently replicating DNA molecules, called plasmids, which can be inserted into the bacterial DNA).‘

According to the Mayo Clinic, ‘In some cases, it may be difficult to determine whether a bacterium or a virus is causing your symptoms. Many ailments — such as pneumonia, meningitis and diarrhea — can be caused by either type of microbe (Viral or Bacterial infection).‘

Such an accumulation of overlapping & contradictory scientific evidence begs the question – has the Medical community misdiagnosed Ebola?

Are we actually dealing with a virus here, or a bacterial strain, or in fact, a composite form of virus/bacteria hybrid?

On close examination, it quickly becomes apparent that MenAfriVac® was rushed into circulation, a cost-cutting measure, without any adequate testing on its potential carcinogenic properties – the end result, a plethora of cases involving post-vaccination neurological damage; notably Guillain–Barré syndrome (GBS).

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‘There have been confirmed case reports of Guillain-Barre Syndrome (GBS), a serious neurologic disorder of peripheral nerves…the most alarming reports were from the village of Guoro in Northern Chad of Africa where at least 40 out of five hundred children that received MenAfrivac vaccine aged between 7 and 18 became paralyzed and these children also suffered convulsions and hallucinations.‘ National Agency for Food & Drugs (NAFDAC)

‘None of the 137 serious adverse events (including 14 deaths) reported in the vaccine studies were assessed to be related to the study vaccines.‘ Review of safety profile on meningococcal A conjugate vaccine from clinical trials, WHO

‘This meningococcal A conjugate vaccine was developed specifically to combat epidemic meningitis in sub-Saharan Africa by a consortium of partners including CDC, PATH, WHO, FDA, the Health Protection Agency and the National Institute for Biological Standards and Control, with funding from the Bill & Melinda Gates Foundation.‘ CDC

The Meningitis Vaccine Project (MVP): ‘Created in June 2001 by a grant from the Bill & Melinda Gates Foundation as a 10-year partnership between WHO and PATH (Program for Appropriate Technology in Health)‘

MVP Mission Statement: ‘to eliminate epidemic meningitis as a public health problem in sub-Saharan Africa through the development, testing, licensure, and widespread use of conjugate meningococcal vaccines.‘

The Meningococcal (Meningitis) Vaccine, MenAfriVac, is defined as a ‘Conjugate Vaccine‘ (containing bacterial capsular polysaccharide joined to a protein to enhance immunogenicity).

Note: ‘The combination of CP conjugate vaccines into a single multivalent injection, however, can result in competition among the different components and adversely affect the immunogenicity of any individual conjugate.‘ Fattom et al., Vaccine 17:126-33 (1999)

‘The MenAfrivac vaccine can be stored under Controlled temperature chain (CTC), up to 40°C for not more than four days immediately prior to administration, provided that the vaccine has not reached its expiry date and the vaccine vial monitor is still valid”. Unopened vaccine vials should be discarded at the end of the four days at 40°C. Reconstituted vaccine should be discarded within six hours.‘ WHO

Note: ‘It is difficult or impossible to reach the entire target population if vaccine is kept in the 2°C to 8°C cold chain.‘

‘There is no evidence that MenAfriVac can cause meningococcal meningitis. Clinical alertness to the possibility of co-incidental meningitis should be maintained.‘ MenAfriVac® (Manufacturer disclaimer)

MenAfriVac® Package insert ‘Each vial contains a lyophilised powder of meningococcal group A polysaccharide conjugated to tetanus toxoid protein and excipients. Each ampoule contains the diluent with aluminium phosphate as adjuvant (the amount does not exceed 1.25 mg per single human dose) and thimerosal (0.01%) as preservative.‘

Note: ‘A small dose of mercury that kills 1 in 100 rats and a dose of aluminum that will kill 1 in 100 rats, when combined have a striking effect: all the rats die. Doses of mercury that have a 1 percent mortality will have a 100 percent mortality rate if some aluminum is there.‘ Dr. Donald Miller, M.D.

The Vaccine components include: ‘Tetanus toxoid + Hydrazine = TT-NH2 & Polysaccharide + NaIO4 = Activated PS.‘

1. Tetanus Toxoid Carrier Protein: ‘Tetanus toxin C-fragment consists of the C-terminal portion of the heavy chain of tetanus toxin…retains the binding and internalization properties associated with intact tetanus toxin. These properties make C-fragment and its conjugates useful in tracing nerve fiber connections in the CNS. List Labs produces C-fragment, Product # 193, from enzyme digested Clostridium tetani toxin.‘

‘Clostridium tetani culture is grown in a peptone-based medium containing an extract of bovine muscle tissue and detoxified with formaldehyde. The bovine muscle tissue used in this medium is US sourced. The detoxified material is then purified by serial ammonium sulfate fractionation and diafiltration, followed by sterile filtration. The toxoid is adsorbed to aluminum potassium sulfate (alum). The adsorbed toxoid is diluted with physiological saline solution (0.85%).

Tetanus Toxoid Adsorbed manufactured by Sanofi Pasteur Inc. is supplied in a unit dose 0.5 mL vial, which contains a trace amount of thimerosal [(mercury derivative), (≤0.3 μg mercury/dose)] from the manufacturing process. Tetanus Toxoid Adsorbed manufactured by Sanofi Pasteur Inc. is also supplied in a 5 mL vial, which contains the preservative thimerosal [(mercury derivative), (25 μg mercury/dose)].‘

Note: ‘The structural gene for tetanus toxin has been cloned and sequenced.‘ Fairweather et al., J. Bacteriol. 165: 21-27 (1986); Fairweather et al., Nuci. Acid Res. 14: 7809-7812 (1986).

2. Hydrazine: ‘Because of the toxicity of hydrazine in humans, it is necessary to monitor this substance’s process control step during the vaccine production.‘

3. NaIO4 9 (Sodium metaperiodate): ‘The substance is toxic to lungs, mucous membranes. Repeated or prolonged exposure to the substance can produce target organs damage.‘

Vaccine excipients: ‘mannitol, sucrose and Tris (hydroxymethyl) aminomethane.‘

Tris (hydroxymethyl) aminomethane: ‘May cause liver and kidney damage. The toxicological properties of this material have not been fully investigated. Hygroscopic (absorbs moisture from the air). Causes eye and skin irritation. May cause respiratory tract irritation.‘

‘GACVS (Global Advisory Committee on Vaccine Safety) supported WHO’s technical guidance that MenAfriVac should be offered to pregnant and lactating women from the African meningitis belt during any stage of pregnancy or lactation, while recommending that a plan be developed to follow up women in antenatal or obstetric clinics, and to monitor pregnancy outcomes by making appropriate comparisons with unvaccinated pregnant women.‘ Extract from report of GACVS meeting of 11-12 June 2014, published in the WHO Weekly Epidemiological Record on 18 July 2014

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The origins of Ebola are linked to a deadly Malaria vaccine formula called ‘Chloroquine’ – which affected only those individuals locally who received the Malaria treatment; while also virally shedding to others in the community who had close contact with the infected (host) vaccinee. In all cases, The typical onset of symptoms leading to Hemorrhagic Fever (what was eventually diagnosed as Ebola) began to manifest within 5 days after receiving the toxic shot.

‘Between 1 September and 24 October 1976, 318 cases of acute viral haemorrhagic fever occurred in northern Zaire. The outbreak was centred in the Bumba Zone of the Equateur Region and most of the cases were recorded within a radius of 70 km of Yambuku, although a few patients sought medical attention in Bumba, Abumombazi, and the capital city of Kinshasa, where individual secondary and tertiary cases occurred. There were 280 deaths, and only 38 serologically confirmed survivors.

The index (first reported) case in this outbreak had onset of symptoms on 1 September 1976, five days after receiving an injection of chloroquine for presumptive malaria at the outpatient clinic at Yambuku Mission Hospital (YMH). He had a clinical remission of his malaria symptoms.

Within one week several other persons who had received injections at YMH also suffered from Ebola haemorrhagic fever, and almost all subsequent cases had either received injections at the hospital or had had close contact with another case. Most of these occurred during the first four weeks of the epidemic, after which time the hospital was closed, 11 of the 17 staff members having died of the disease.

All ages and both sexes were affected, but women 15-29 years of age had the highest incidence of disease, a phenomenon strongly related to attendance at prenatal and outpatient clinics at the hospital where they received injections. The overall secondary attack rate was about 5%, although it ranged to 20% among close relatives such as spouses, parent or child, and brother or sister.‘ Report of an International Commission, World Health Organization, 1978

1. ‘The index (first reported) case in this outbreak had onset of symptoms on 1 September 1976, five days after receiving an injection of chloroquine for presumptive malaria ‘

2. ‘Within one week several other persons who had received injections at YMH also suffered from Ebola haemorrhagic fever.’

3. ‘almost all subsequent cases had either received injections at the hospital or had had close contact (vaccine-derived viral shedding) with another case.’

Note to those Doctors & Virologists unaware of this crucial information: Chloroquine (“drug” treatment for Malaria) was indeed INJECTED into those Africans who subsequently contracted Ebola (typical symptoms manifesting within 5-7 days). It has since been given primarily in a pill form; accepting those ‘acute attacks of malaria when the patient is unable to swallow’. However in 1976, in Zaire, Africa, safety protocols were unavailable or ignored – with dire consequences.

The following (severe) side effects are associated with chloroquine injection; Abnormal Heart Electrical Signals, Abnormal Liver Function Tests, Abnormally Low Blood Pressure, Acquired Decrease of All Cells in the Blood, Decreased Blood Platelets, Decreased Neutrophils a Type of White Blood Cell, Deficiency of Granulocytes a Type of White Blood Cell, Disease of the Muscle of the Heart with Enlargement, Hepatitis, Increased Eosinophils in the Blood, Life Threatening Allergic Reaction, Low Blood Counts due to Bone Marrow Failure, Stevens-Johnson Syndrome, Toxic Epidermal Necrolysis.‘ WebMD


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Ebola Virus: ‘Generally, the abrupt onset of Ebola haemorrhagic fever follows an incubation period of 2–21 days (mean 4–10) and is characterised by fever, chills, malaise, and myalgia. The subsequent signs and symptoms indicate multisystem involvement and include systemic (prostration), gastrointestinal (anorexia, nausea, vomiting, abdominal pain, diarrhoea), respiratory (chest pain, shortness of breath, cough, nasal discharge), vascular (conjunctival injection, postural hypotension, oedema), and neurological (headache, confusion, coma) manifestations.

Haemorrhagic manifestations arise during the peak of the illness and include petechiae, ecchymoses, uncontrolled oozing from venepuncture sites, mucosal haemorrhages, and post-mortem evidence of visceral haemorrhagic effusions. A macropapular rash associated with varying severity of erythema and desquamate can often be noted by day 5–7 of the illness; this symptom is a valuable differential diagnostic feature and is usually followed by desquamation in survivors. Abdominal pain is sometimes associated with hyperamylasaemia and true pancreatitis. In later stages, shock, convulsions, severe metabolic disturbances, and, in more than half the cases, diffuse coagulopathy supervene.‘ Heinz Feldmann, MD and Thomas W Geisbert, PhD, The Lancet

‘The four Ebola strains are termed as follows: Zaire, Sudan, Tai Forest, and Bundibugyo virus, with Zaire being the most lethal strain. A fifth strain termed Reston has been found in the Philippines. The strain infects primates, pigs, and humans and causes few if any symptoms and no deaths in humans. Most outbreaks of the more lethal strains of Ebola have occurred in Africa and mainly in small- or medium-sized towns.‘ MedicineNet

”The mean incubation period was estimated to be 12.7 days (standard deviation 4.31 days), indicating that about 4.1% of patients may have incubation periods longer than 21 days.‘ Incubation Period of Ebola Hemorrhagic Virus Subtype Zaire

‘An important distinction of Ebola virus from other Mononegavirales is the production of a soluble glycoprotein, which is the primary product of the GP gene, and gets secreted to large quantities from infected cells.‘ National Institutes of Health

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The epidemiology of Yellow Fever also bares striking resemblance to Ebola, given the distinct characteristics & potential virulence common to each virus:

1. an incubation period lasting upwards of 1 week (‘Physical symptoms usually appear 3–6 days after’)

2. an array of flu-like symptoms during the initial stages, including (‘fever, muscle pain, particularly backache, headache, shivering, loss of appetite, and nausea or vomiting’)

3. leading to varying degrees of internal “blackish” bruising & widespread hemorrhaging (‘gastrointestinal bleeding, haematuria, skin petechiae, ecchymoses,’)

4. followed by rapid systemic deterioration, marked by Kidney failure, often leading to death (‘About 20%–50% of patients with hepato-renal failure die, usually 7–10 days after the onset of disease’)

‘Typically, the disease onset is abrupt, with fever, muscle pain, particularly backache, headache, shivering, loss of appetite, and nausea or vomiting. Congestion of the conjunctivae and face are common, as well as relative bradycardia in the presence of fever. The patient is usually viraemic during this period, which lasts for approximately 3–6 days.

In approximately 15% of infected persons, the illness recurs in more severe form after a brief remission of 2–24 hours. Symptoms include fever, nausea, vomiting, epigastric pain, jaundice, renal insufficiency, and cardiovascular instability. A bleeding diathesis can occur causing gastrointestinal bleeding, haematuria, skin petechiae, ecchymoses, epistaxis, and bleeding from the gums and needle-puncture sites.


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Physical findings include scleral and dermal jaundice, haemorrhages at different sites and epigastric tenderness without hepatic enlargement. The haemorrhagic manifestations are caused by reduced synthesis of clotting factors as well as by a consumptive coagulopathy.

About 20%–50% of patients with hepato-renal failure die, usually 7–10 days after the onset of disease. Patients surviving YF may experience prolonged weakness and fatigue, but healing of the liver and kidney injuries is usually complete.‘ WHO Position Paper – June 2011

‘Yellow fever vaccine-associated viscerotropic disease (YEL-AVD) is a rare and serious adverse event associated with administration of the yellow fever vaccine. YEL-AVD is an illness similar to wild-type yellow fever, in which the vaccine virus proliferates in multiple organs, causing multiple organ dysfunction syndrome or multiorgan failure and death in at least 60% of cases. Initial symptoms of YEL-AVD are nonspecific and can include the following: fever, malaise, headache, myalgia, vomiting, and diarrhea. More severe cases can progress to hepatic (liver), renal (kidney), or respiratory insufficiency or failure; hypotension; thrombocytopenia; and coagulopathy (inability to regulate clotting causing massive hemorrhaging).‘ CDC – History, Epidemiology, and Vaccination Information

‘Yellow fever vaccine-associated viscerotropic disease (YEL-AVD) is clinically indistinguishable from wild-type yellow fever illness. Most YEL-AVD reports describe patients with fever and multiple organ system failure, and often death (17 deaths/29 cases worldwide).‘ The American Journal of Tropical Medicine and Hygiene

‘The present YF vaccines are based on a wild-type YF virus isolated in Ghana in 1927. Numerous mutations in the viral structural and non-structural genes have led to the attenuated variant 17D. This attenuated vaccine virus exists in 2 sub-strains (17D-204 and 17DD) which share 99.9% sequence homology. Nucleotide sequencing has shown differences between these vaccine strains and the wild-type Asibi strain, affecting 20 amino acids. Virus with the resulting phenotype is non-transmissible by mosquitoes. Both sub-strains are used in vaccines prepared by culturing the virus in embryonated eggs. The vaccine contains sorbitol and/or gelatine as a stabilizer and is lyophilized. No preservative is added.‘ WHO Position Paper on Yellow Fever Vaccine

Based on preliminary reports from field doctors in Africa, Doctors in Belgium examining blood samples from the 1976 Zaire outbreak were initially expecting Yellow Fever, NOT Ebola. ‘The researchers in Zaire who had sent it couldn’t identify the virus, simply labeling it, “Yellow Fever?”‘

In 1994, another Ebola outbreak (in northeastern Gabon, bordering the Congo) was mistaken for Yellow Fever, this time based on actual clinical findings – ‘Yellow fever (YF) virus was first diagnosed in serum by use of polymerase chain reaction followed by blotting,‘

This subsequently led to the institution of a Yellow Fever vaccination campaign. It was only later, that doctors determined: ‘some aspects of this epidemic were atypical of YF infection, so a retrospective check for other etiologic agents was undertaken. Ebola (EBO) virus was found to be present concomitantly (joined together/co-mingling) with YF (Yellow Fever) virus in the epidemic.‘

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This current version of Ebola virus had 40 years to spread to outlying regions. It never did.

How did the Zaire strain of Ebola get to West Africa from about 3,500 km away from where it was first identified in 1976?

How does a virus that has remained dormant, relatively stable, isolated, suddenly manifest in areas well outside its traditional territory?

With a little help from the Centres for Disease Control (proliferation), that’s how.

Even the CDC Director admits they are baffled by the unprecedented concentration of cases outside the typical range,

‘For more than four decades, Ebola virus had only been diagnosed in Central or Eastern Africa. Then late this past March, the first cases of Ebola began appearing in a surprising part of the continent. The outbreak in Guinea was the first sign that the virus had made the jump across the continent. Ebola then spread quickly to Sierra Leone and Liberia, and then to Nigeria.‘ Tom Frieden, MD, Director, US Centers for Disease Control and Prevention, Atlanta, Georgia

‘No virus that causes disease in humans has ever been known to mutate to change its mode of transmission.‘ Mainstream Media misinformation

In truth, no virus is fully modified or attenuated or killed during the vaccine manufacturing process. All vaccines, by their very nature, play off each other, generate a “synergistic” chain-reaction triggering further (more insidious) infections & disorders. In many cases the very signature disease/disorder they claim to protect you against is PRECISELY that which they inadvertently spread; albeit a more virulent “transforming” strain of the primary pathogen.

Essentially, ALL Viral vaccines become “weaponized” through the various stages of Vaccine development; further metastasizing in the vaccine host: ‘Mutations that can occur when the vaccine virus replicates in the body may result in more a virulent strain.‘



SOURCE

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In practical terms, a synergy factor inevitably occurs when multiple ingredients such as heavy metals, live (attenuated/modified) viruses/or strands of DNA-RNA “heat treated virus”, antibiotic(s), formaldehyde, detergent(s), diploid cells (aborted fetal tissue), mycoplasma, phenol dye & excipient buffers are combined together in a vial mixture, generating a bio-active (electrical) chemical reaction – worsened by combinations with post-vaccination Prescription drugs; frequently seen as the tipping point which triggers/hastens an escalation of adverse neurological symptoms, a cascading degeneration (reduced Mitochondrial & Metabolic capacity) leading to varying degrees of auto-immune (multi-systemic) failure in the body.

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‘The viruses are generally attenuated on the basis of only a few mutations and have a considerable chance of reverting to wild-type thereby causing the very disease in vaccine recipients that they are aimed to prevent.‘ GIT Laboratory Journal

‘Despite the advantages of live, attenuated vaccines, there are some downsides. It is the nature of living things to change, or mutate, and the organisms used in live, attenuated vaccines are no different. The remote possibility exists that an attenuated microbe in the vaccine could revert to a virulent form and cause disease.’ US National Institute of Allergy and Infectious Diseases

‘One concern that must be considered is the potential for the vaccine virus to revert to a form capable of causing disease. Mutations that can occur when the vaccine virus replicates in the body may result in more a virulent strain. This is very unlikely, as the vaccine virus’s ability to replicate at all is limited; however, it is taken into consideration when developing an attenuated vaccine.

It is worth noting that mutations are somewhat common with the oral polio vaccine (OPV), a live vaccine that is ingested instead of injected. The vaccine virus can mutate into a virulent form and result in rare cases of paralytic polio. For this reason, OPV is no longer used in the United States, and has been replaced on the Recommended Childhood Immunization Schedule by the inactivated polio vaccine (IPV).‘ College of Physicians, Philadelphia

“One vaccine decreases cell-mediated immunity by 50%, two vaccines by 70%…all triple vaccines (MMR, DTaP) markedly impair cell-mediated immunity, which predisposes to recurrent viral infections, especially otitis media, as well as yeast and fungi infections.” World-renowned Immunologist Dr. H.H. Fudenberg

‘Adventitious agents (mutable viruses/cross-contamination) could theoretically enter a viral vaccine through any of these ingredients (cell substrates, vaccine seed, tissue culture reagents, stabilizers).’ FDA

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The United States Government (Secretary of the Dept. of Health) secured the Patent & “de facto” proprietary rights to both Ebola & Yellow Fever Virus well before 2014. By extension, this gave the CDC (including National Institute of Allergy and Infectious Diseases & National Institutes of Health) carte blanche to experiment with either strain at will - a five year head-start on Ebola, and a fourteen year head-start on Yellow Fever.

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The Ebola strain now circulating has clearly undergone significant mutagenic changes in a laboratory, alterations in the nucleotide sequencing that enable it to spread more quickly and efficiently that ever before.

Despite claims by the World Health Organization that Ebola is strictly a bloodborne pathogen which ‘spreads through human-to-human transmission via direct contact (through broken skin or mucous membranes) with the blood, secretions, organs or other bodily fluids of infected people, and with surfaces and materials (e.g. bedding, clothing) contaminated with these fluids’, evidence to the contrary, from multiple sources is challenging this Official narrative.

The Ebola Virus is now seemingly airborne.

‘Under conditions of the current study, transmission of ZEBOV (Zaire Ebola Virus) could have occurred either by inhalation (of aerosol or larger droplets), and/or droplet inoculation of eyes and mucosal surfaces and/or by fomites due to droplets generated during the cleaning of the room. Infection of all four macaques in an environment, preventing direct contact between the two species and between the macaques themselves, supports the concept of airborne transmission…the presence of Ebola virus antigen in some of the respiratory epithelial cells in the lungs of all macaques suggest that the airways were one of the routes involved in the acquisition of infection, consistent with previous reports..‘ National Centre for Foreign Animal Disease & National Microbiology Laboratory, Winnipeg, Canada 05 November 2012

Note: ‘Our findings support the hypothesis that airborne transmission may contribute to ZEBOV (Zaire Ebola Virus) spread, specifically from pigs to primates, and may need to be considered in assessing transmission from animals to humans in general.‘

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The Ebola & Aids (HIV) Virus share one precise common thread, a key protein capable of shutting down the body’s Immune system, by disabling what are known as T-cells.

‘T cells contribute to immune defenses in two major ways: Some direct and regulate immune responses…by communicating with other cells. Some stimulate nearby B cells to produce antibodies, others call in microbe-gobbling cells called phagocytes, and still others activate other T cells.‘ National Institute of Allergies & Infectious Diseases

“You know the (Ebola) virus, it’s like ‘shock and awe.’ It’s like over within a week. I mean the virus grows very quickly and it kills off the very cells you need to mount your immune response.” Dr. Kartik Chandran, Whitehead Institute, Harvard Medical School, Albert Einstein College of Medicine

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‘Ebola virus’s ability to enter cells is reminiscent of the Trojan Horse used by the ancient Greeks to defeat their archenemies. Ebola virus binds to the host cell’s outer membrane, and a portion of host cell membrane then surrounds the virus and pinches off, creating an endosome — a membrane-bound bubble inside the cell (see image). Endosomes carry their viral stowaways deep within the cell and eventually mature into lysosomes — tiny enzyme-filled structures that digest and recycle cellular debris.

The viruses captive in the lysosome manage to escape destruction by exploiting components of the cell to gain entry to the cytoplasm, the substance between the cell membrane and the nucleus where the virus can replicate. But the identities of many of these components have remained unknown.‘ Albert Einstein College of Medicine, 08/24/2011

‘Our screen uncovered 67 mutations disrupting all six members of the homotypic fusion and vacuole protein-sorting (HOPS) multisubunit tethering complex, which is involved in the fusion of endosomes to lysosomes, and 39 independent mutations that disrupt the endo/lysosomal cholesterol transporter protein Niemann–Pick C1 (NPC1).‘ Ebola virus entry requires the cholesterol transporter Niemann–Pick C1, International Weekly Journal of Science, 08/24/2011

‘Niemann-Pick disease type C1 is a lysosomal storage disease caused by a mutation in the NPC1 gene. NPC1 encodes an integral membrane protein containing sequence motifs thought to be consistent with a role in intracellular transport of cholesterol to post-lysosomal destinations. Mutations in NPC1 have also been linked with obesity, HIV-AIDS, and Ebola virus.‘
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A 1972 report (Bulletin 47) issued by the World Health Organization referred to an immune virus requested which would selectively destroy the Human T Cell System, to be distributed in conjunction with a Nationwide vaccination program “to observe the results”.
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This coincided precisely with the extensive Small Pox vaccination program in central Africa & Hepatitis B program (Africa & throughout the Americas etc)– shortly preceding the outbreak of Aids in Africa, America & elsewhere. The determining factor most common in Aids (and Ebola) victims is the breakdown of the T Cell System in the body. Just another disturbing coincidence.
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“There is a blueprint, the 1971 research logic of the US Special (HIV) Virus program…a virus that only targets certain persons – as is evidenced by the epidemiology. Here is the final phase, the clinical trials. It was placed in the Small Pox vaccines that went to Africa. Every epidemiology that we have regarding the beginning of HIV & Aids shows that as Small Pox ended, HIV & Aids began in mass in Africa. HIV and Aids began in mass in the late 1970’s as a result of the US Special Virus program and the complementation of that vaccine (Small Pox vaccine program in Africa) with this special virus (T-Cell disruptor component – authorized by Henry Kissinger) that shows the development of HIV over a period from 1962-1978.

How dare you have a Federal Virus program that precedes the greatest onslaught of murder in the history of the world, and you don’t want to acknowledge the program, and you certainly don’t want to review it. The people demand it. This Federal program lies at the heart of HIV & Aids and it needs to be reviewed.” Dr. Boyd Graves (formal testimony given shortly before his premature death)

The whole criteria for identifying Ebola is, in and of itself, skewed. These viruses have undergone so many changes, through decades of (unmonitored) laboratory experimentation, re-engineering & chemical synthesis and genetic replication via vaccine programs, they no longer resemble anything close to the naturally occurring, “wild strains” previously found in the environment.

Irrespective of whether we are confronting a vaccine-derived hybrid (mutagenic) strain of bacterial Meningitis here, a vaccine-derived hybrid strain of Yellow Fever, a deadly variant of Malaria, or, in fact, a laboratory-derived hybrid strain of the Ebola Virus (essentially a composite of the laboratory produced Aids syndrome) the so-called vanguard of Health “Authority”, chiefly the CDC & WHO, are purposefully focusing on a Vaccine & Drug response to this current health crisis, while ignoring the fact that the Ebola Virus can only thrive in a body starved of Selenium – thereby depriving our communities of critical information in a time of national emergency.

The Ebola Virus can ONLY thrive in a body starved of Selenium. In fact ALL Ebola Virus victims, those who typically succumb to Hemorrhagic fever, viral replication (infected blood) and excessive hemorrhaging of the blood leading to death, concurrently suffer from acute malnutrition, marked by extreme Selenium deficiency in the body.

Selenium is an essential trace mineral & anti-oxidant, a primary stop-gap which enables the human body to adapt to (overcome) any viral infections circulating in the environment, and helps to prevent the typical Ebola-type symptoms (chiefly excessive hemorrhaging) from taking hold and ultimately killing the host (vaccinee).

Selenium helps regulate Thyroid function and your overall metabolism, primarily by preventing an over-abundance of free-radicals in the body, converts T4 (free thyroxine) to T3 (triiodothyronine), supported by Vitamin E. Selenium deficiency also inhibits the body’s ability to process nutrients effectively.

Natural sources rich in Selenium include Brazil nuts, Sunflower seeds & Food Grade Diatomaceo​us Earth (“fossilized shell flour”).

Note: Selenium is a major piece in the puzzle; however, given the insidious nature of Ebola, proper guidelines respecting an overall holistic health protocol must be followed – therefore a balanced approach combining all essential trace minerals & antioxidants, including phytonutrients, is needed.

‘Ebola is classified as a “hemorrhagic fever” virus, and produces the characteristic hemorrhaging due to the formation of blood clots (“disseminated intravascular coagulation”), leading to the obstruction and rupture of small blood capillaries.

SOURCE

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It is very well documented that Se (Selenium) plays a significant role in the regulation of blood clotting via its effects on the thromboxane/prostacyclin ratio.

Se (Selenium) has an anti-clotting effect, whereas Se (Selenium) deficiency has a pro-clotting or thrombotic effect. Se (Selenium) deficiency has been associated with thrombosis and even hemorrhaging, which has been documented in a number of animals with severe Se (Selenium) deficiency (often artificially induced), but is almost never seen in humans, probably because such an extreme Se (Selenium) deficiency is rarely attained due to the diversity of human diet.

Our analysis suggests that severe Ebola infections could produce an artificial and extreme Se (Selenium) depletion, resulting in extensive cellular damage due to lipid peroxidation, combined with enhanced thrombosis. This could also contribute to the associated immune deficiency that has been observed in Ebola infections.

If viruses like HIV-1 (Aids), coxsackievirus B3 (linked to Meningitis) and Ebola do encode selenoproteins, why does all the evidence suggest that dietary Se (Selenium) inhibits viral replication, whereas Se (Selenium) deficiency triggers replication?‘ Journal of Orthomolecular Medicine, 1995

Note: ‘…extensive cellular damage due to lipid peroxidation, combined with enhanced thrombosis (excessive blood-clotting – the result of vaccine-derived auto-immune failure in the body).‘

Lipid peroxidation is associated with cellular damage resulting from oxidative stress (or Ischemia), which inhibits the capacity of cellular antioxidants, vital to natural immunity, by the unleashing of free radicals. – Scientific verification of demyelination linked to mitochondrial breakdown, caused by the intervention of (vaccine-derived) aluminum on early childhood development in the brain.
A World Health Organization-led consortium of Vaccine Industry manufacturing giants & Government health departments are now racing to capitalize on this burgeoning health crisis; introducing clinical trials on a “promising experimental Ebola vaccine” – spearheaded by none other than the National Institute of Allergy and Infectious Diseases (NIAID).

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WHO High-level meeting on Ebola vaccines access and financing (23 October 2014) – Summary Report: ‘The meeting concluded that neither affected countries nor industry should be left alone to bear the burden should lawsuits arise following possible adverse reactions to an Ebola vaccine...The principle of “pursuing all vaccines until they fail” was put forward as a wise way to maintain momentum in responding to an emergency of this scale. Representatives from industry acknowledged the investment risks they are willingly undertaking despite knowledge that a vaccine might fail or not be needed in the end.‘

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‘The recent increase in funding for Ebola vaccine research is also enabling GSK (GlaxoSmithKline) to begin manufacturing at least 10,000 additional doses of the vaccine, even as the first clinical trials are occurring.‘ Global Defence

‘Development of the vaccine candidate is progressing at an unprecedented rate, with first phase 1 safety trials with the vaccine candidate underway in the USA, UK and Mali, and further trials due to start in the coming weeks..‘ GSK update on current development status of the GSK/NIH Ebola vaccine candidate (18/10/2014)

‘GlaxoSmithKline’s monthly production capacity for purified bulk vaccine was expected to rise from the current figure of 24,000 doses to 230,000 by April 2015, if they can be filled for release. NewLink’s bulk vaccine manufacturing capacity for the Canadian vaccine was noted to vary, according to the dose selected, from 52,000 doses to 5.2 million doses anticipated for the first quarter of 2015.‘ WHO

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The genie is out of the bottle. Once this vaccine, and other similar concoctions, are distributed locally & internationally, the Ebola Virus protein epitope (laboratory-produced clone of Niemann-Pick C1) will spread exponentially, undergoing further mutagenic changes through viral shedding in remote communities; those otherwise completed segregated from the traditional epicentres of the outbreak.

Then we will have a REAL epidemic on our hands.

The current virulent strain of the Ebola Virus is a (weaponized) variant of Yellow Fever Virus, invariably crossed with Malaria, Bacterial Septicemia (Septic shock) & HIV Aids. We have come to the end of the road; the culmination of decades of the most toxic vaccines ever created, gestating and mutating throughout the population of Sub-Saharan Africa – manifesting in the coveted Virus-Bacterial hybrid the Rockefellers have sought for decades.

There is no plausible explanation for the presence of a T-Cell disrupting protein epitope (identical to the Aids Syndrome signature HIV component – designed specifically to target the Human Immune System) embedded in the current Ebola Virus strain: ‘Mutations in NPC1 (Niemann–Pick C1) have also been linked with HIV-AIDS, and Ebola virus.‘

This breed of insidious pathogen does not just manifest out of thin air. Nature is NOT your adversary. Nature does not create an antigen purposely to wipe out an entire sector of the population. There has to have been a catalyst here to produce such a specific Immune-system crippling agent.

Through the annals of history, outbreaks of disease, plague & life-threatening epidemics were primarily the result of over-crowding, marked by insufficient hygiene, sanitation & nutrition. In this day & age, given proper access to clean drinking water, modern sanitation methods & a steady organic diet, there is simply no excuse, here in the West, for the exponential surge in cases of early childhood diseases & disorders now gripping our communities.

The overwhelming body of scientific evidence points to one critical determining factor in the rise of mutagenic viruses & systemic erosion of natural immunity: multi-generational community-wide exposure to the Standard Immunization regime, in particular, those viral vaccines fixed on the schedule which combine multiple live attenuated viruses. In Africa, the odds are far worse than elsewhere.

This is the time when families have to step up and shake off our complacency, to get active NOW. Ebola is going to become as common as the common flu, unless we take charge now. We have to smash this corrupt Industry now. The CDC has proven themselves to be systemic liars. We have to take charge of our destiny and stop this cycle now.

We will not stop this onslaught unless we band together. We will not stop mandatory vaccinations unless we band together as a community.

It is incumbent upon us, as a global community of parents & concerned individuals alike, to take action and ensure that any dire scenario of this magnitude does not manifest. As always, the paradigm shift toward self-sufficiency & self-awareness begins with you.

See: VRM: Measles Report

See: VRM: Vaccines Do Contain Aborted Human Fetal Tissue

See: VRM: The Rise of Mutagenic Viruses

VRM: The Autism Report http://vaccineresistancemovement.org/?p=10185

VRM: Worldwide Autism Study Direct link to study: http://study.vaccineresistancemovement.org/

VRM: The Problem With Vaccines Part 1 http://vaccineresistancemovement.org/?p=488

VRM: Vaccine Clinic – A Concise Compendium To The Problem With Vaccines http://vaccineresistancemovement.org/?p=6278

VRM: The Problem With Vaccines Part 2 – Synergistic Effect of Heavy Metal Toxicity On The Body http://vaccineresistancemovement.org/?p=6097

VRM: The Problem With Vaccines Part 3 – Synthetic Genomics & The Death Of Natural Immunity http://vaccineresistancemovement.org/?p=6880

VRM: A Concise Compendium To The Problem With Vaccines Part 3 – Synthetic Genomics & The Death Of Natural Immunity http://vaccineresistancemovement.org/?p=7283

VRM: The Problem With Vaccines Part 4 – Primary Aspects of Vaccine Toxicity Affecting Body http://vaccineresistancemovement.org/?p=8787

VRM: The Problem With Vaccines Part 5A – Detoxification & Restoration of the Body http://vaccineresistancemovement.org/?p=8836

VRM: The Problem With Vaccines Part 5B – Detoxification & Restoration of the Body http://vaccineresistancemovement.org/?p=8847

VRM: PCV Vaccine Exposed – Breeding Ground For Staphylococcus Aureus http://vaccineresistancemovement.org/?p=9431

VRM: Pandemic Preparedness & The Dark Agenda Ahead http://vaccineresistancemovement.org/?p=9460

VRM: Polio – United Nations & The Great Cull http://vaccineresistancemovement.org/?p=4916

VRM: The Re-emergence of Polio in The Third World (compliments of the World Health Organization & Bill Gates) http://vaccineresistancemovement.org/?p=10091

VRM: Weaponized Polio & The African Green Monkey Conundrum http://vaccineresistancemovement.org/?p=10727

VRM: Mandatory Vaccinatio​ns – How They Will Be Implemente​d http://vaccineresistancemovement.org/?p=11806

VRM: The Confidenti​al Case-files of GlaxoSmith​Kline – Cover-up, Deferral & Denial of Responsibi​lity for Vaccine-re​lated Premature Deaths http://vaccineresistancemovement.org/?p=12242

VRM: Primary Reasons Not To Get The Flu Shot http://vaccineresistancemovement.org/?p=12642

VRM: The Flu Report http://vaccineresistancemovement.org/?p=9226

VRM: Vaccine Ingredients http://vaccineresistancemovement.org/?p=979

VRM: Safe Alternatives to Vaccines http://vaccineresistancemovement.org/?p=662%EF%BB%BF

VRM: Family Charts Gradual Decline Of Daughter http://vaccineresistancemovement.org/?p=3156

VRM: Health Matters Part 1 http://vaccineresistancemovement.org/?p=6719

VRM: Health Matters Part 2 http://vaccineresistancemovement.org/?p=6746%EF%BB%BF

VRM: Alternative Cancer Cures That Work http://vaccineresistancemovement.org/?p=3729

VRM: Pregnancy Tips http://vaccineresistancemovement.org/?p=3270

VRM: H1N1 Shot Reactions – Miscarriages http://vaccineresistancemovement.org/?p=943

VRM: The Vanishing Sperm Count http://vaccineresistancemovement.org/?p=4639

VRM: H1N1 Vaccine Surplus From 2009 Reveals Growing Distrust of Gov’t & WHO http://vaccineresistancemovement.org/?p=4969

VRM: Flu Death Statistics – WHO & The Big Lie http://vaccineresistancemovement.org/?p=784

VRM: Vaccine Industry Deception, Propaganda & Media Collusion http://vaccineresistancemovement.org/?p=197

VRM: Birth of Medical & Scientific Dictatorship – Future Scenarios http://vaccineresistancemovement.org/?p=997

VRM: H1N1 Bio-weaponry Incorporated http://vaccineresistancemovement.org/?p=884

VRM: Aids & The WHO Connection – Criminal Intent http://vaccineresistancemovement.org/?p=1749

VRM: Morgellons Syndrome & Chemtrails http://vaccineresistancemovement.org/?p=839

VRM: Council On Foreign Relations 10/16/09- Major Influence on Government Vaccine Policy http://vaccineresistancemovement.org/?p=1880

VRM: Closed Door CDC Meeting Reveals Industry Cover-up Of Heavy Metal Toxicity In Vaccines http://vaccineresistancemovement.org/?p=5935

VRM: The Rockefeller Foundation Drafts A Post-Pandemic Scenario http://vaccineresistancemovement.org/?p=5102

VRM: World Health Organization & Vaccine Manufacturers Implicated In Massive H1N1 Financial Scam Involving Kickbacks & Cover-ups http://vaccineresistancemovement.org/?p=4610

VRM Live – 01/28/11: Vaccine Resistance Movement founder Joel Lord discusses Synthetic Genomics, cloned cell vaccine technology & the death of natural immunity, gutter journalism & Dr. Wakefield’s imminent vindication with ‘Truth to Power’ host Paul Mabelis. http://www.blogtalkradio.com/empradio/2011/01/28/truth-to-power-thursday

VRM Live - 11/04/10: Vaccine Resistance Movement founder Joel Lord lays out the whole vaccine process with Paul Mabelis; including heavy metal toxicity, synergy, pregnancy issues & the basic principles of natural health at risk. http://www.blogtalkradio.com/show.aspx?userurl=empradio&year=2010&month=11&day=05&url=truth-to-power-thursday

VRM Live - 09/24/10: Vaccine Resistance Movement Founder Joel Lord & activist/radio host Jesse Calhoun lay it all out tonite. Topics include the VRM Worldwide Autism Study, Scientific/Medical dictatorship, Natural Rights & Vaccine Industry fraud exposed. Special thanks to host Paul Mabelis. http://www.blogtalkradio.com/empradio/2010/09/24/truth-to-power-thursday

If you appreciate the efforts to bring this information forward do consider making a donation. Any amount, no matter how small will help enable me to carry on this invaluable research. See Paypal link on the VRM website (click on ‘Donate’ tab in upper right corner). Thank you all.
SOURCE

FROM COMMENTS SECTION:

Vaccine Resistance Movement goes live! The most controversial angle out there on this whole scandal. Has the Medical community misdiagnosed Ebola? http://www.blogtalkradio.com/publica...llie-o-elkordy

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Warren Pollock-Pompeii Type of Event Coming

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TOPIC(S):

Inverted Totalitarianism
Ebola & Inverted Totalitarianism
A Low Statistical Risk
Being Sold to Benefit Pharmaceutical & Vaccine Makers
Consumerism has grown to be Worldwide
Jobs Created through Ebola
Rationalization & Dissonance
End of a Era
Could Be 70,000 people per Day Dead for a 5 year Period
Rationalization, An Abyss, Followed by Either a Dark Age or a Renaissance
Help Yourself by Being Alert, Being Flexible, By Being Aware that Might Only Be Able to Carry Things on Your Back
Adjustment Period Could be Very Long

LateNite in the Midlands

Ebola Conspiracy Exposed : Dr. Leonard Horowitz & Sherri Kane

3rd November 2014

This will be an amazing informative interview on Ebola with two Liberian activists, Putugah Takpaw Phenom, King Jauz.
We will also be joined by Thomas Duncan's brother and nephew. Thomas Duncan was the Liberian man who was the first Ebola patient to die in the U.S. of Ebola.

Source: https://youtube.com/watch?v=StDfxApJw4k

Spreaker Link

Farrakhan: Justifiable Homicide: Black Youth in Peril-American Gangster 3/3

https://www.youtube.com/watch?v=u0Y0rlyPSmk#t=5m28s

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The U.S. government’s desire for world depopulation

In a national security memo dated April 24, 1974 titled, “Implications of Worldwide Population Growth for the United States Security and Overseas Interest,” Henry Kissinger, the Secretary of State under Richard Nixon, indicated: “Depopulation should be the highest priority of foreign policy towards the Third World.” Depopulation—to depopulate something means: “To ravage, to ruin, to reduce the population of, especially by violence, disease, etc.” Mr. Kissinger continued, “The United States economy will require large and increasing amounts of minerals from abroad, especially from less developed countries”—this means they are going to destroy the population of mainly Third World countries.

The policy paper titled, “Rebuilding America’s Defenses,” is the “white paper” of the neoconservatives in their Project for a New American Century (PNAC). On page 60 it states:


A genotype is, “A race or a kind; it is the fundamental constitution of an organism in terms of its hereditary factors.” This means that these wise scientists of death are making pathogens, which is something that can cause a disease. They are creating this as a means of depopulating our planet of undesirables, a process called culling the population. To cull means: “To pick out; to sellect in order to discard or destroy; to discard or destroy unwarranted parts; something rejected as not being up to standard.” So, if you are poor and ignorant; if you are Black or Brown, you are being selected for destruction.

Means and methods of depopulation

What is the method that they are going to use to depopulate? Through civil wars in which depleted uranium and Agent Orange are used. Currently, there are 39 states in America that have already been polluted by depleted uranium. Look at the target areas: El Salvador—what is there in El Salvador that America wants? It is oil. America already has a military base, embassy, and CIA operatives working to kill off the Indigenous population so that nobody can threaten their takeover of oil.

Another method is disease infection through bio-weapons such as Ebola and AIDS, which are race targeting weapons. There is a weapon that can be put in a room where there are Black and White people, and it will kill only the Black and spare the White, because it is a genotype weapon that is designed for your genes, for your race, for your kind.

*********

Look at this, the crops contaminated with altered DNA that sterilizes the consumer. I know you all love McDonald’s and Wendy’s, and all of the fast food stores that are predominately in the Black and Latino community, but how do you kill a fool? You kill him through his natural desire to eat, and you kill him and her through their taste buds. It tastes good, but it is not good.

The forced sterilization programs that are going on right now among Native Americans are also going on among you with new birth control devices. It’s not an accident that when I was coming up there was no sex on television; when you saw a man and a woman enter a room, a nature scene would come up and then you were left to your imagination. Today, there isn’t anything left to the imagination.

The U.S. government is killing people by toxic food, water, air and medicine. Turn on your TV and just stop a moment and count the number of food and pill commercials. The pharmaceutical companies are marketing death by making medicines to make us sick, so as to make more money out of treating our illnesses before we die. Well, they’re going to kill you anyway, but they’re going to get rich in the process of killing you with your pains.

Then, the U.S. government creates mass hysteria: “Oh my God, the terrorists are coming! We’d better kill them over there before we have to fight them over here. The terrorists are coming!”—and you are sitting there in your house terrified because the TV is just herding you like sheep.

*********

From 1932-1972, wicked White scientists inflicted Black men in Tuskegee, Alabama with syphilis. They knew that these Black men had syphilis, but did not let the men know that they were being used. The men copulated with many Black women, spreading syphilis through our community, and when they became terribly sick, those “doctors” would never treat the men for syphilis. Thirty years later; 40 years later, the truth comes out.

What kind of mind could take you in a room and give you an inoculation that you think is one thing, but it is something else? See, nobody could do this but a devil. I’m not talking about some spook devil—I’m talking about a real devil that can breathe and has hands and a brain to think evil!

I don’t want anyone to think I’m a racist; if any of you that are here that think of yourselves as White, don’t look at me like I’m a hater, because everything I say, I can prove it and will die on it! I’m not against any race; I am against the evil that men of that race are planning against my people.

Selective breeding: The rulers and the ruled

In the Bible, Paul said, “We war not against flesh and blood but against principalities and powers and the rulers of the darkness of this world and spiritual wickedness that’s up in high places.” What I want to do is bring the high places right down so you can look at these people.

Bertran Russell, a British philosopher and mathematician, said: “Gradually, by selective breeding, the congenital differences between rulers and the ruled will increase until they become almost two different species.”

Then there is Margaret Sanger, who in 1939, began to target Blacks by creating what is called the “Negro Project” to promote birth control and sterilization specifically within the Black community. She supposed it would help solve the problem of “Southern Negro poverty”—see how they put a nice face on murder?

Ms. Sanger said that in order to carry out the plan, she sought the support of prominent, Black ministers and political leaders: “The most successful educational approach to the Negro is through a religious appeal.” We don’t want to get the word out that we want to exterminate the Negro population and the minister is the man who can straighten out the idea if it occurs to any one of their more rebellious members.

It is dangerous to be a preacher today that’s going to be an apologist for a system that is destructive of your people; it is dangerous to be a political leader who is an apologist for the conspiracy and the conspirators after you know.

The Black community’s civil war

The world is at war, and some of us know and some of us don’t. The Bible teaches that the people in the days of Noah were boogying, partying and having a good time when the end came. And the homosexuals in Sodom and Gomorrah, they were also having a good time when the end came. The enemy today has got you, now, bumping and grinding, but the end is in sight and he keeps you away from seeing by partying and looking at yourself. In the 1960s, we knew who the enemy was.

In the 1960s, we could turn on the TV at night and see Martin Luther King Jr.; we would see the Civil Rights leaders; Bull Conner. We would see fire hoses and dogs and cattle prods. And we’d see the enemy beating our people down. We knew who the enemy was! But two generations later, you go in the Black community now and ask them, “Who is the enemy?” We have become the enemy to one another.

When you look at the murder rate in the Black community, this is civil war. In one year, out of the 20,000 homicides throughout America, 46 percent of them were “us killing us.” That means in one year, nearly 9,000 young Black men died from murder—not by a White police force, but by us. Look at all of the funerals that are happening inside the community right now. Mothers, you are taking your son, your daughter to their final resting place because of gang conflict; it was something going on in the community. How can a White policeman’s killing of a Black Brother warrant more response from Black community leaders than our shooting of one another?

*********

The enemy is watching the disunity of Black leaders, who argue and fight each other in the public. The enemy says, “Oh well, what the hell, they’re not united, so let’s show them that we ain’t got no fear of what they are doing.” So they took Mychal Bell of The Jena Six, picked him right back up on an old charge and sentenced him to 18 months in jail. That is a horrible miscarriage of justice. So Father Michael Pfleger, Harry Belafonte, Reverend Al Sharpton and others decided to have a march on the Justice Department, because the Justice Department is really failing Black people. It’s true. I sent a message to them, stating that I will join them in a march on the Justice Department because it has failed, but I said, “Look at the statistics: It is not them killing us from the police side of this thing—it is us killing us. So, I don’t mind marching with you to the Justice Department, but let us mobilize our people and let us go in our community and get our young people and stop them from the senseless killing of one another, and then fight to give them jobs and opportunity.”

See, if we do that, then our marching is not a race thing; it’s a justice thing. But if you’re not willing to confront the murder and mayhem that’s going on in our own community, then you’re not serious. Perhaps you are looking to get some points by maybe going to the Justice Department, but after the march is over, the Justice Department will say, “Well, them Negroes ain’t together. Let’s murder some more,” because we’re not serious about White people’s murder of Blacks if we don’t stop murder among ourselves.

*********

More Black men have died in one year than U.S. soldiers in Afghanistan and Iraq have died in five years. Every night on the news they are telling us the number of U.S. soldiers that have died on a daily and monthly basis. In one month, the highest death toll may have been around 100. But ask yourself: How many young Black men died in one week, in one month, in the ’hoods throughout America? See, there isn’t anyone focusing on that. This is a silent, civil war going on that is being ignored that has mothers and grandmothers taking their babies to the cemetery.

President’s right to declare Federal Martial Law

Brothers and Sisters, you are a beautiful people. We just have to work as hard as we can to make the devil’s plan unsuccessful. The scripture teaches, “If God had not shortened those days for His elect’s sake, no soul would be left alive.” That is how dark it is going to get. The next type of war is urban conflict, and what they are doing in Baghdad, Iraq right now is what they are going to do in the inner cities of America—kick in your doors, well armed, looking for weapons.

Let me tell you what is about to go down: All law enforcement inside the United States must be by police, sheriffs and the National Guard, but when federal troops come in, that violates the “Posse Comitatus Law.” In a stealth maneuver, President George W. Bush, on October 17, 2006, signed into law that which would make it easy for him to dec1are Federal Martial Law. He did this by revising the Insurrection Act, which is a set of laws that limits the President’s ability to deploy troops within the United States.

President Bush seized this power under executive orders. The Federal Martial Law states that if there is any major public emergency, the President may employ the Armed Forces, including the National Guard, in federal service to restore public order and to enforce the laws of the United States when as a result of a natural disaster, epidemic or other serious public health emergency, terrorist attack or incident or any other condition. In any state or possession of the United States, if the President determines that domestic violence has occurred to such an extent that the constituted authorities of the state or possession are incapable in maintaining public order, then in order to suppress the disorder in any state, any insurrection, domestic violence, unlawful combination or conspiracy the President can dec1are Martial Law that suspends the Constitution.

The following are Executive Orders that Pres. Bush, as well as presidents before him—Carter and Bush, Sr.—have signed into law:

Executive Order 10999: Federal seizure of all means of transportation including cars, trucks or vehicles of any kind and total control over all highways, seaports and water ways—this means in an emergency, your car or truck doesn’t belong to you anymore; the government can seize your car and say they need it.

Executive Order 11000: Federal seizure of American people for work forces under federal supervision, including the splitting up of families if the government so desires—this means that if such a thing happens, they can pull us all in and put us to work on whatever project the government says, you have no authority to resist. To resist is death.

Executive Order 11001: Federal seizure of all health, education and welfare facilities, both public and private.

Executive Order 11002: Empowers the Post Master General to register every single person in the United States. “No more draft; we’re just taking you now.”

Executive Order 11003: Federal seizure of all airports and aircraft.

Executive Order 11004: Federal seizure of all housing and finances—that the government would take your house; take your money, this means your bank account is not yours. What you thought you had hidden in a safety deposit box is not yours.

The United States government has the authority to enforce relocation, meaning if they think you need to be relocated like they did the Native Americans on that long march, they’ll just do it. They can establish new locations for population; relocate communities and build new housing with public funds. Seize all railroads, inland waterways and storage facilities. And if you resist—forced vaccinations; they can force you to take a needle.

What you are seeing is the development of a police state. So the next coming months and years are going to be difficult, and that is why we have to work to save our youth.

*********

I believe that we can take our young people off the street, bring them to the mosque or to the church, not to make you a Muslim or a Christian or whatever, but to just give you some hope. Some of you don’t realize, even if you don’t go to school, that there are skills that you could be taught that could be useful in rebuilding the inner cities. Take the craftsmen; those who know plumbing, roofing, brick masons, electricians, and let us take our skilled people and teach the young people a trade. It’s so simple, but it can be done! Teach all these young Brothers a trade that they can use now and watch how you’re going to use it. Look at all of the vacant lots our cities; we should go to our city council leaders and say, “We want to put our young people to work. Give us the lot and we’ll go to work building low cost housing units, selling it to our people, putting the money in a treasury that belongs to the youth.” Then when the young people develop enough money, they can start buying property in the community where they live. When this happens, this makes those social engineers say, “These Negroes are foiling our plans,” because we can offer our youth a GED that means something; we can offer our youth a college degree that means something. Our youth don’t have to lie around here thinking that there is no hope. There’s plenty of hope! But we’ve got to go back home now and begin to change the way we think and the way we act.

Thank you for reading these words. As-Salaam Alaikum.

SOURCE

And... Reality starts to sink in........

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RIP, “the Ebola threat”: How a toxic narrative served its political purpose
There are no cases of Ebola in the U.S., and panic seems to have subsided. It's almost like an election just ended!
The Ebola was supposed to have killed us all by now. Or at least a couple hundred million of us, give or take. Jaundiced, hemorrhagic carcasses were supposed to be lining the streets, while the few survivors retreated to isolated bunkers in the Badlands or the Rocky Mountains to weather the storm and procreate for the eventual reconstruction of civil society.

If the level of attention and panic displayed in the media and in politics toward “the Ebola threat” were proportional to the reality on the ground, this is what America on Nov. 11, 2014, should have looked like: a nightmarish hellscape of near-extinction, somewhat comical in its rapid erasure of human progress. Of all the possibilities, it was the Ebola that did us in. Who’da thunk it? You just have to laugh.

As it stands, though, there are currently zero (0) cases of Ebola in the United States. Craig Spencer, the New York doctor who was isolated after testing positive for the Ebola hemorrhagic virus in late October, is now free of the virus. He has been released from the hospital and is being fêted. Look at him, hugging that big softie lug of a mayor they have in New York City. “It is a good feeling to hug a hero,” the mayor said. Everyone’s having a great time.

When news came out last night about Spencer’s release, it was seemingly the first big news story about Ebola in the United States in the past week — quite a change from even two weeks ago, and for weeks before that, when Ebola was the top news story in the United States. It was pure frenzy. After Spencer tested positive for Ebola, we had governors throwing healthy women in parking lot tents in Newark. That nurse, who bravely won her freedom, is apparently going to move from her home in Maine to get away from all the attention and start over. She needn’t bother. The panic is over.

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http://www.salon.com/2014/11/12/r_i_...tical_purpose/

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Posted by TargeT

And... Reality starts to sink in........

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RIP, “the Ebola threat”: How a toxic narrative served its political purpose
There are no cases of Ebola in the U.S., and panic seems to have subsided. It's almost like an election just ended!
The Ebola was supposed to have killed us all by now. Or at least a couple hundred million of us, give or take. Jaundiced, hemorrhagic carcasses were supposed to be lining the streets, while the few survivors retreated to isolated bunkers in the Badlands or the Rocky Mountains to weather the storm and procreate for the eventual reconstruction of civil society.

If the level of attention and panic displayed in the media and in politics toward “the Ebola threat” were proportional to the reality on the ground, this is what America on Nov. 11, 2014, should have looked like: a nightmarish hellscape of near-extinction, somewhat comical in its rapid erasure of human progress. Of all the possibilities, it was the Ebola that did us in. Who’da thunk it? You just have to laugh.

As it stands, though, there are currently zero (0) cases of Ebola in the United States. Craig Spencer, the New York doctor who was isolated after testing positive for the Ebola hemorrhagic virus in late October, is now free of the virus. He has been released from the hospital and is being fêted. Look at him, hugging that big softie lug of a mayor they have in New York City. “It is a good feeling to hug a hero,” the mayor said. Everyone’s having a great time.

When news came out last night about Spencer’s release, it was seemingly the first big news story about Ebola in the United States in the past week — quite a change from even two weeks ago, and for weeks before that, when Ebola was the top news story in the United States. It was pure frenzy. After Spencer tested positive for Ebola, we had governors throwing healthy women in parking lot tents in Newark. That nurse, who bravely won her freedom, is apparently going to move from her home in Maine to get away from all the attention and start over. She needn’t bother. The panic is over.

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http://www.salon.com/2014/11/12/r_i_...tical_purpose/

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Its got me wondering Just HOW(?) did these people in West Africa really come down with this so-called Ebola virus???

Following RAP song says it to me quite clear...

Vaccines - A Bad Rap!

https://youtube.com/watch?v=PbSpPs05YAc

_________________EDIT_________________

http://curezone.com/upload/_T_Forums...e_Campaign.png

The ebola pandemic began in late February in the former French colony of Guinea while UN agencies were conducting nationwide vaccine campaigns for three other diseases in rural districts. The simultaneous eruptions of this filovirus virus in widely separated zones strongly suggests that the virulent Zaire ebola strain (ZEBOV) was deliberately introduced to test an antidote in secret trials on unsuspecting humans.

The cross-border escape of ebola into neighboring Sierra Leone and Liberia indicates something went terribly wrong during the illegal clinical trials by a major pharmaceutical company. Through the lens darkly, the release of ebola may well have been an act of biowarfare in the post-colonial struggle to control mineral-rich West Africa

Earlier this year, rural residents eagerly stood in line to receive vaccinations from foreign-funded medical programs. Since the cover-up of the initial outbreak, however, panicked West Africans rural folk are terrified of any treatment from international aid programs for fear of a rumored genocide campaign. The mass hysteria is also fueled in a region traditionally targeted by Western pedophiles by the fact that filovirus survives longer in semen than in other body fluids, a point that resulted in murderous attacks on young men believed to be homosexuals. Ebola detonated fear and loathing, and perhaps that is exactly the intended objective of a destabilization strategy.

This ongoing series of investigative journalism reports on the ebola crisis exposes how West Africans are largely justified in their distrust of the Western aid agencies that unleashed, whether by mistake or deliberate intent, the most virulent virus known to man.

Guilt Without Doubt

A pair of earlier articles by this writer examined the British and American roles in developing ebola into a biological weapon and its antidotes into commercial products. This third essay examines the strange coincidence of the earliest breakout in Guinea with three major vaccine campaigns conducted by the World Health Organization (WHO) and the UN children’s agency UNICEF. At least two of the vaccination programs were implemented by Medicins Sans Frontieres (MSF, or Doctors Without Borders), while some of those vaccines were produced by Sanofi Pasteur, a French pharmaceutical whose major shareholder is the Rothschild Group. This report uncovers the French connection to the African ebola pandemic.

Human Guinea Pigs

The guinea pig used in laboratory testing of new drugs is neither a pig nor from Guinea, since its natural habitat is on another continent, specifically the Andes. The test subjects at the time of the very first ebola outbreaks in Guinea were not rodents or pigs; they were humans.

The mystery at the heart of the ebola outbreak is how the 1995 Zaire (ZEBOV) strain, which originated in Central Africa some 4,000 km to the east in Congolese (Zairean) provinces of Central Africa, managed to suddenly resurface now a decade later in Guinea, West Africa. Since no evidence of ebola infections in transit has been detected at airports, ports or highways, the initial infections must have come from one of either two alternative routes:

- First, the possibility of an anonymous “Patient A”, a survivor of the devastating 1995 Zaire pandemic, perhaps a doctor or medical worker who was a carrier of the dormant virus into Guinea. An example of a Patient A is Patrick Sawyer, the infected American resident of Liberia who first transmitted ebola to Nigeria. No attempt has been made by the national health ministry or international agencies to trace and identify the original ebola case in Guinea. So far, not a shred of evidence has surfaced to indicate&nbs p;the very first victim to be a foreigner or a Guinean who had traveled abroad.

- Second, the absence of a Patient A leaves the prospect of an unauthorized test in humans of a new antidote for ebola in rural Guinea, done under the cover of a vaccination program for another disease. Whether the covert clinical trial’s purpose was civilian health or military use of an antibody-based antidote cannot be determined as of yet.

The reason for suspecting a vaccine campaign rather than an individual carrier is due to the fact that the ebola contagion did not start at a single geographic center and then spread outward along the roads. Instead. simultaneous outbreaks of multiple cases occurred in widely separated parts of rural Guinea, indicating a highly organized effort to infect residents in different locations in the same time-frame.

The ebola outbreak in early March coincided with three separate vaccination campaigns countrywide: a cholera oral vaccine effort by Medicins Sans Frontieres under the WHO; and UNICEF-funded prevention programs against meningitis and polio:

- The MSF-WHO project administered the anti-cholera vaccine Shanchol. The drug producer Shanta Biotechnics in Hyderabad, India, is a wholly owned subsidiary of Sanofi Pasteur based in Lyon, France. Formerly known as Sanofi Aventis, the pharmaceutical controlled by major shareholders L’Oreal and the Rothschild Group.

- The oral polio vaccine (OPV) drive funded by UNICEF was based on a pathogen seed strain developed by Sanofi Pasteur, which operates the world’s largest polio vaccine production facility.

- The meningitis vaccine MenAfrVac, was produced by the Serum Institute of India, owned by tycoon Cyrus Poonawalla, under development funding from the Bill and Melinda Gates Foundation. In 2013, a UNICEF drive in Chad with the same drug resulted in 40 child deaths from vaccine-linked symptom. MSF participated in the West African anti-meningitis project.

Medicins Sanofi Frontieres

While focused on the French role, it would be unjust not to shed light on the American chief of the UN children’s agency. UNICEF executive directory Anthony Lake has an ideal career background for the post of protector of children worldwide. Tony Lake was National Security Advisor to President Bill Clinton responsible for US military interventions, including: the Bosnia-Herzegovina war against the Yugoslav federation; the Battle of Mogadishu in Somalia better known as “Blackhawk Down”; and Operation Uphold Democracy in Haiti. An ardent& nbsp;Zionist convert to Judaism, he is the perfect boss to dispense risky vaccines in Muslim-majority Guinea.

One of Lake’s closest international allies during the Balkans war, who shares his policy of “expansionist democracy” and “humanitarian intervention” is French-Jewish hero Bernard Kouchner. The co-founder of Medicins Sans Frontier, the leftist politician-doctor was appointed Foreign Minister under neoconservative President Nicholas Sarkozy. Before succumbing to the temptation of shouting “Physician heal thyself!”, let’s turn back to tracking ebola.

MSF, which translates into English as Doctors Without Borders, promotes itself as a brave band of selfless physicians who spend their time and own savings on helping the poor in global hot spots. Many of the volunteers, to their individual credit and moral goodness, actually exemplify the public-relations image, never realizing that MSF corporate sponsors include the Bill Gates-founded behemoth Microsoft, Goldman Sachs, AIG, Morgan Stanley, Bank of America, BlackRock, Bloomberg and the French advertising giant Havas.

A rogue’s gallery of corporate predators, if ever there was, the donor list is notably absent of major pharmaceuticals, since it would be a conflict of interest to charitably dispense vaccines from a drug company while being paid for the free advertising. To avoid appearances of ethical impropriety on a global scale, the UN through its agencies WHO and UNICEF foots the bill, the major pharms get the profits, and MSF executives with their horde of bright-eyed volunteers dispense the low-end vaccines on the suffering mass es.

Not to discourage idealist doctors from a worthy cause, there is the undeniable attraction of safari fever and Orientalist exoticism for a surgeon from Pittsburg or Strasbourg to take part in this hybrid of “Amazing Race” and Club Med. Now off with the kid gloves: While posturing as principled ethical “witnesses” to human misery, the functional role of MSF role is as a conveyor belt dumping vaccines from major pharmaceuticals onto low-income and poorly educated populations of the developing world.

Repeated dosages of potent toxins on populations with poor health, which no public-health agency in the Western world dares attempt inside its own borders, can have harmful side effects, especially on children. The casualties of vaccination have gone unreported by the media and buried under official cover-ups. Even worse, vaccine programs could well have been used to conceal human testing of antibodies that originated in biological warfare labs for the purpose of mass murder of entire nations.

Best Laid Plans

Doctors Without Frontiers (MSF), once based in Paris and now in Geneva, comes under a dark cloud of suspicion because its distribution of a two-step anti-cholera vaccine. The dosages must be taken a fortnight apart, and this repeat procedure likely provided the pretext for an ebola-testing team to insert the ebola virus into the victims’ bodies and later return to dispense the antidote of monoclonal antibodies (Mab).

(This is not to say that MSF was knowingly involved as an organization but that its “federation” style of management leaves a lot of maneuvering space for an unethical doctor to infiltrate a country program on behalf a client pharmaceutical.)

After exposure to the ebola virus, a patient shows symptoms of high fever, vomiting and diarrhea, no less than 8 days later and likelier after two weeks. Re-arriving on schedule, the covert drug-testing team administers the anti-ebola antibodies as “the second dose of cholera vaccine”. The perfect crime of illegal human testing should have gone off without a hitch.

A problem arises, however, when many of the test subjects fall sick in less than two weeks and are unable to walk dozens of kilometers to the vaccine centers. With much of the original cohort of human test subjects absent for the antidote, and ebola out of control in the hinterland, the secret clinical trial free-falls toward a pit of liability and legal action. Disappointed operations managers for the sponsoring pharmaceutical order the exfiltration of their medical agents out of Guinea, leaving hundreds of victims to die in excruciating pain as the contagion spreads. Does anyone in Paris or Geneva really care? Don’t choke in laughter.

The Guinea outbreak was not reported by WHO until 6 weeks after the initial round of infections in February, which is quite odd considering the armies of medical workers afield in the countryside during those three vaccine campaigns. By contrast, the MSF office in next-door Senegal knew about the Guinean ebola contagion less than a month after outbreak.

Inside and Outside the Death Zones

On the map of Africa, the Republic of Guinea (not to be confused with Equatorial Guinea on the coast of Central Africa) is shaped like a reversed letter C, looping off the Atlantic shore and curving southeast into the interior. The Niger River cuts across the country from east to west; two separate regions along its banks were the centers of the initial ebola outbreak.

The earliest infections were concentrated in the inland prefectures of Guecedo and Macenta on the interior borders of Sierra Leone and Liberia. The second-most affected region was closer to the Atlantic coast in the districts of Boffa and Telimele and the nearby island-capital of Conakry. The deaths in Conakry were concentrated at Donka Hospital, the prime treatment center.

What is striking about the Red Cross-Red Crescent Society map of the outbreak zones was the lack of infections over a wide swath along the border with Senegal, where MSF keeps its regional headquarters with a 300-member staff, which includes 80 foreigners. The reason can be attributed to the drier climate of Senegal, yet to the contrary ebola infections were reported near Guinea’s northern border with arid Mali, which is in the Sahara Desert.

On first reports of the outbreak, the Pasteur Institute branch in Dakar, Senegal, dispatched a mobile microbiology laboratory to Conakry at the request of the Guinean Ministry of Health. Meanwhile, the German-funded Bernhard-Nocht Institute of Tropical Medicine office in Ghana cooperated with WHO to set up a mobile lab in Gueckedou Prefecture.

MSF staffers inside Guinea cooperated with the government’s Ministry of Health effort to set up isolation rooms in local clinics and hospitals along with blood-sample collection centers. Despite assurances from WHO and CDC that ebola is not transmitted through water or air, more than 100 nurses and doctors, including Sierra Leone’s top ebola expert, have died so far. Misinformation about ebola transmission is inexcusable when the 1995 Zaire outbreak was first spread by the washing of corpses.

Turning Panic Into Profit

Another appalling surprise came in June with the “second wave” of apparently more virulent ebola infections across Sierra Leone, even after the pandemic was coming under control in Guinea. This second breakout could be related to a mutation caused by the introduction of monoclonal antibodies during the covert antidote tests. Confronted by Mab-activated immune responses in humans, the virus could be expected to adapt by increasing the velocity of its docking with unprotected human blood cells. If mutation is confirmed, then all Mab-based&n bsp;serums should be banned due to the potential emergence of the unstoppable “super-virus”, a modified strain of ebola on steroids.

News media have focused on two potential cures for ebola issued by biotech companies ZMapp and Tekmira, both of them essentially business fronts for patent-sharing consortia. Whichever company gains approval from an FDA, ready to overlook the possibility of driving mutations, will be sure to win huge supplier contracts from the WHO and the US Department of Defense.

The dark horse in the foot race to profit from the ebola panic is France-based Sanofi Pasteur. The world’s third-largest pharmaceutical, under CEO Serge Weinberg, has earned a reputation for come-from-behind success in the final rounds of clinical trials in humans. Weinberg scored a coup in wooing his new chief scientist Gary Nabel from his position as head of viral immunology research at the National Institutes of Health (NIH).

The Sanofi strategy for ebola is being kept under wraps by its biotech partner Sutro Biopharma based in San Francisco. Sutro managing director John Freund, MD, is a former Morgan Stanley executive who built its health-care portfolio. The Sutro-Sanofi-Nabel monoclonal antibody (Mab) strategy, using tumor antigen Mabs, is listed for purposes “undisclosed”. The use of antibodies from abnormal or cancerous cells is the same as the cell-fusion method used by their now better-known competitor ZMapp.

For the unethical executive, it is tempting to conduct drug tests in humans without wasting years on monkey trials, as was done by wartime Japan’s Unit 731 and by Dr. Joseph Mengele. In 2008, Sanofi was accused of conducting secret trials of an untested H5N1 vaccine on 350 homeless people in Poland, killing at least 21 and causing the hospitalization of 200 others, according to the Telegraph of London.

The cold-blooded spread of a hemorrhagic fever cannot be attributed solely to corporate greed, since biodefense security is also a motive. The West African outbreak was likely linked to a dual-use experiment, for application in tropical health and as a biowarfare shield, as shown in the two earlier essays in this series.

On the List of Suspects

While a signatory of the Biological Weapons Convention, France did not sign aboard until 1984, providing sufficient time to guise its biowarfare research under civilian lab coats. The nation that produced brilliant scientists like Louis Pasteur, the pioneer discoverer of vaccines, France was one of the leading research centers in biological warfare, weaponizing anthrax, salmonella, chorela and rindepest, toxins that resonate with the French passion for cuisine.

The postwar French military had none of the ability to commandeer Germany’s formidable bioweapons technology, as did Britain, the US and Soviet Union. Instead of focusing on the German passion for “germ” warfare, French medical researchers skipped ahead by concentrating on molecular biology, in which viruses are of intense interest for their interactions with the proteins in cell membranes and nucleic acids. Due to their high-tech sophistication, it is rare for French research centers to be caught red-handed, as happened when the Pasteu r Institute in Iran was discovered to be crafting aflatoxin for the Shah’s military.

French biologists moreover have had deep experience in tropical pathogens from their own African colonies and the Belgian Congo. The nation’s most notable achievement in recent years was Luc Montagnier’s isolation of the HIV, which notably he claims was not of African origin, indicating the Pasteur Institute’s vast library of biological agents.

The French are masters of ambiguity and dissimulation, and so there is no chance for a French military attache to be seen strutting around Guinea or Sierra Leone like a Jean Reno. The CDC in Liberia, in contrast, with its 50-member forward squad marching in protective gear stands out like a sore thumb.

Therefore, don’t forget to put the Elysee Palace on the suspect list if ebola is found out to be a biowarfare attack to destabilize West Africa and redraw the geopolitical boundaries. The French Army is largest foreign force on the continent. To borrow Churchill’s metaphor of nesting dolls, antibodies are a riddle wrapped in the mystery of ebola inside an enigma of biological warfare.

The other Sanofi project in Guinea involving a polio vaccine campaign could have enabled the follow-up work of checking on the success rate of the secret antibody tests. If so, it was a miserable failure or perhaps a wild success. In either case, the pharmaceutical and biotech industries will have profited handsomely from the ebola crisis when biodefense-research generals, high civil servants and UN bureaucrats sheepishly sign multimillion-euro R&D contracts.
Feverish Africa

After rural West Africans realized that vaccination programs coincided with the outbreak of Zaire ebola, foreign-funded medical staffers were assaulted by angry mobs and an ebola treatment center in Sierra Leone was burned to the ground. When medicine is exposed to be the problem and not a solution, the military has to be called in to quell public rebellion. The boundaries of every country in the region are now sealed by troops, and so the truth behind this epidemic will probably be buried with the victims.

As for MSF, UNICEF, WHO, CDC, NIH, USAMRIID and the rest of the alphabet soup of the hypocritical oafs of pharmaco-witchcraft, the herd instinct for self-preservation prevents any honest disclosure. As each day passes and casualties mount, the onus for the crime weighs heavier. A trustworthy investigation into this fast-spreading pandemic and prosecution of the perpetrators in a court of law have all the chances of snowfall in Zaire.

Yoichi Shimatsu, a Thailand-based science writer, organized public-health seminars by leading microbiologists and herbalists during the SARS outbreak in Hong Kong and the avian influenza crisis across Southeast Asia.

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Posted by turiya

Its got me wondering Just HOW(?) did these people in West Africa really come down with this so-called Ebola virus???

Following RAP song says it to me quite clear...

Vaccines - A Bad Rap!

https://youtube.com/watch?v=PbSpPs05YAc

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I think it's very plausible/probable that one of the Red Cross vaccination programs in Africa introduced Ebola to thousands, perhaps unwittingly. This could be how some local doctors and health workers were included in the infected groups, however, since Ebola works best against the malnourished and chronically vitamin D deficient population of west Africa mostly those people died.. but the tainted vaccines could not continue or would easily be figured out... and thus the complete disappearance of Ebola

I believe the above more than anything I've seen from the MSM, but with no evidence I would not take an absolute stance on it.

edit:
haha turiya, looks like your edit agrees with my post ;) (or my post agrees with your edit) ;) except I see it's the UN not redcross (both are shady IMO)

Source: https://youtube.com/watch?v=lAz-F1QnyCk

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Posted by TargeT

Source: https://youtube.com/watch?v=lAz-F1QnyCk

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LoL, Just absolutely side-splitting. Thanks TargeT! Gonna have to pass this one around a bit.

In fact, if you consider the more cynical aspect of what is behind the very possibility that this Ebola outbreak was created... to ramp up the fear factor so that the populations of nations would run into the arms of the WHO (World Health Organization) & the supposed "protection" & "security" that their vaccines are supposed to provide, its a kind of Master Plan for population reduction as to what the bastard, Bill Gates, has proposed in his TED Talk. Even though, its not the first time that the WHO has hidden a "sterilization agent" within vaccines (See the Jim Stone Article), consider the following agenda roll-out.


I sent one of my clients the following information:
My client is a prominent academician at a university well known for research in the field of public health. Actually, it was the follow-up to my informing him, as an aside to out brief conversation on Ebola, that the U.S. government & the CDC owned the patent on a manufactured strain of Ebola. He didn't want to believe me. So I said I would send him the patent number, along with the abstract it came with.

After doing that, he said that he was knowledgeable enough to understand everything in that abstract. And it looked like I was correct about it. It appears as though the patent is to a strain of Ebola that was man-made. I responded back by saying "yes, its so the patent owners could reap the royalties from any vaccine that was later developed."

Here's how the rest of that e-mail went...

Ebola Patent No. CA2741523A1
http://www.google.com/patents/CA2741523A1

http://curezone.com/upload/_T_Forums...2741523_A1.png
Patent for a Man-made Strain of Ebola

Timeline:

1) October 26, 2009 - The Ebola patent filing date.

2) February 2010 - Bill Gates Gives His "Innovating to Zero" TED Talk, making the following unbelievable statement:

"Now if we do a really great job on new vaccines, health care, reproductive health services - we could lower that [population factor] by, perhaps 10 - 15%."

--Bill Gates (February, 2010)
(An obvious glaring question would be: If vaccines were so good for humanity, then why would their use be connected with reducing population? The logical view would be that people would live longer, hence populations would increase.

3) April 29, 2010 - Ebola Patent is published.

4) September 10, 2010 - Bill Gates announces that the Bill & Melinda Gates Foundation will spend $50 million on Ebola to develop vaccines & provide supplies.

https://youtube.com/watch?v=tD0zR1XVDlI

5) Tuesday, May 17, 2011. Bill Gates, Addresses the 64th World Health Assembly in Geneva, of which, as you well know the World Health Organization is a functioning arm, the following:

"And for all 193 member States, you must make vaccines a high priority in your health systems, to ensure that all your children have access to all vaccines now & to the new vaccines that have recently become available."--Bill Gates at the U.N. Speech

https://youtube.com/watch?v=QqePDrifFNo

6) Of course the West African Ebola Outbreak proceeds as planned... (citation needed). Death rates are high, U.S. military in place in Liberia ready to implement mandatory vaccination campaign - (for the good of the people & the planet).

7) Thursday Nov 6, 2014. WHO Vaccines Found Spiked with Infertility Drugs
Although, as I said at the beginning of this post... its not the first time that the WHO has hidden a "sterilization agent" within vaccines (See the Jim Stone Article),...
With the onslaught & publicity that this unprecedented Ebola outbreak has precipitated, the WHO & CDC have made it "easy pickens" as the third world is now set-up to vaccinate the whole continent of Africa to make the populations less likely that these people will be able procreate future generations.

Kissinger's, the Rothschilds & Rockefellers, with assistance from philanthropist, Bill Gates, & his Foundation (& Trustee, Warren Buffet) got to be grinning ear to ear, behind the scenes.

‘A mass sterilization exercise’:
Kenyan doctors find anti-fertility agent in U.N. tetanus vaccine
Population Control Thu Nov 6, 2014

UPDATE (Nov. 12): Kenya's government has launched an investigation into the Catholic Church's allegations. See follow up article here.

Kenya’s Catholic bishops are charging two United Nations organizations with sterilizing millions of girls and women under cover of an anti-tetanus inoculation program sponsored by the Kenyan government.

According to a statement released Tuesday by the Kenya Catholic Doctors Association, the organization has found an antigen that causes miscarriages in a vaccine being administered to 2.3 million girls and women by the World Health Organization and UNICEF. Priests throughout Kenya reportedly are advising their congregations to refuse the vaccine.

“We sent six samples from around Kenya to laboratories in South Africa. They tested positive for the HCG antigen,” Dr. Muhame Ngare of the Mercy Medical Centre in Nairobi told LifeSiteNews. “They were all laced with HCG.”

Dr. Ngare, spokesman for the Kenya Catholic Doctors Association, stated in a bulletin released November 4, “This proved right our worst fears; that this WHO campaign is not about eradicating neonatal tetanus but a well-coordinated forceful population control mass sterilization exercise using a proven fertility regulating vaccine. This evidence was presented to the Ministry of Health before the third round of immunization but was ignored.”

But the government says the vaccine is safe. Health Minister James Macharia even told the BBC, “I would recommend my own daughter and wife to take it because I entirely 100% agree with it and have confidence it has no adverse health effects.”

And Dr. Collins Tabu, head of the Health Ministry’s immunization branch, told the Kenyan Nation, that “there is no other additive in the vaccine other than the tetanus antigen.”

Tabu said the same vaccine has been used for 30 years in Kenya. Moreover, “there are women who were vaccinated in October 2013 and March this year who are expectant. Therefore we deny that the vaccines are laced with contraceptives.”

Newspaper stories also report women getting pregnant after being vaccinated.

Responds Dr. Ngare: “Either we are lying or the government is lying. But ask yourself, ‘What reason do the Catholic doctors have for lying?’” Dr. Ngare added: “The Catholic Church has been here in Kenya providing health care and vaccinating for 100 years for longer than Kenya has existed as a country.”

Dr. Ngare told LifeSiteNews that several things alerted doctors in the Church’s far-flung medical system of 54 hospitals, 83 health centres, and 17 medical and nursing schools to the possibility the anti-tetanus campaign was secretly an anti-fertility campaign.

https://youtube.com/watch?v=UExQeqGP1j4

Why, they ask does it involve an unprecedented five shots (or “jabs” as they are known, in Kenya) over more than two years and why is it applied only to women of child-bearing years, and why is it not being conducted without the usual fanfare of government publicity?

“Usually we give a series three shots over two to three years, we give it anyone who comes into the clinic with an open wound, men, women or children.” said Dr. Ngare. “If this is intended to inoculate children in the womb, why give it to girls starting at 15 years? You cannot get married till you are 18.” The usual way to vaccinate children is to wait till they are six weeks old.”

But it is the five-vaccination regime that is most alarming. “The only time tetanus vaccine has been given in five doses is when it is used as a carrier in fertility regulating vaccines laced with the pregnancy hormone, Human Chorionic Gonadotropin (HCG) developed by WHO in 1992.”

It is HCG that has been found in all six samples sent to the University of Nairobi medical laboratory and another in South Africa. The bishops and doctors warn that injecting women with HCG , which mimics a natural hormone produced by pregnant women, causes them to develop antibodies against it. When they do get pregnant, and produce their own version of HCG, it triggers the production of antibodies that cause a miscarriage.

“We knew that the last time this vaccination with five injections has been used was in Mexico in 1993 and Nicaragua and the Philippines in 1994,” said Dr. Ngare. “It didn’t cause miscarriages till three years later,” which is why, he added, the counterclaims that women who got the vaccination recently and then got pregnant are meaningless.

Ngare said WHO tried to bring the same anti-fertility program into Kenya in the 1990s. “We alerted the government and it stopped the vaccination. But this time they haven’t done so.”

Ngare also contrasted the secrecy of this campaign with the usual fanfare accompanying national vaccination efforts. “They usually bring all the stakeholders together three months before the campaign, like they did with polio a little while ago. And they use staff in all the centres to give out the vaccine.” But with this anti-tetanus campaign, “only a few operatives from the government are allowed to give it out. They come with a police escort. They take it away with them when they are finished. Why not leave it with the local medical staff to administer?”

Brian Clowes of Human Life International in Virginia told LifeSite News that WHO was not involved in the Nicaragua, Mexican and Philippines campaigns. “They try to maintain a spotless record. They let organizations like United Nations Population Fund and USAID do the dirty work.”

In the previous cases, said Clowes, the vaccinators insisted their product was pure until it was shown not to be. Then they claimed the positive tests for HCG were isolated, accidental contaminations in the manufacturing process.

LifeSiteNews has obtained a UN report on an August 1992 meeting at its world headquarters in Geneva of 10 scientists from “Australia, Europe, India and the U.S.A” and 10 “women’s health advocates” from around the world, to discuss the use of “fertility regulating vaccines.” It describes the “anti-Human Chorionic Gonadotropin vaccine” as the most advanced.

One million Kenyan women and girls have been vaccinated so far with another 1.3 million to go. The vaccination is targeting women, according to the government, in order to inoculate their children in the womb against tetanus as well. The government says 550 children die of tetanus yearly.

In covering the contest of words the pro-government Nation found plenty of women who had been vaccinated and were now pregnant, even one who was the wife of a former Catholic priest who left the Church to marry. The paper ignored Kenya’s reliance on the Catholic medical system, while setting the bishops’ stand in a questionable historical context of irrational responses “largely based on religious beliefs,” the more recent murder of vaccination teams in Nigeria, and even of CIA conspiracy theories.

Why would the UN want to suppress the population in developing countries? “Racism,” is Brian Clowes’ first explanation. “Also, the developed countries want to get hold of their natural resources. And lately, there is the whole bogus global warming thing.”

Dr. Ngare said it was the Catholic Church’s hope that the government could have resolved the matter quietly by testing the vaccine. “But the government has chosen to be combative,” forcing Kenya’s bishops and Catholic doctors to go public.

WHO’s Kenyan office and several WHO media contacts in Washington, D.C. failed to respond to LifeSiteNews enquiries over a 24-hour period.
SOURCE

There is a famous quote by Solzhenitsyn that rings quite true in all of this. Its a quote that Leonard Horowitz has included in the publishing of his best seller, Emerging Diseases: AIDS & Ebola - Nature, Accident or Intentional?:

"To do evil, a human being must first believe that what they are doing is good. It is ideology that gives devil-doing its long-sought justification."--Solzhenitsy

Quote:

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Posted by turiya

In fact, if you consider the more cynical aspect of what is behind the very possibility that this Ebola outbreak was created... to ramp up the fear factor so that the populations of nations would run into the arms of the WHO (World Health Organization) & the supposed "protection" & "security" that their vaccines are supposed to provide, its a kind of Master Plan for population reduction as to what the bastard, Bill Gates, has proposed in his TED Talk.

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I think this is absolutely the case... except the fear campaign did not take hold well enough, though it surely did try very hard; I'm sure copious notes were taken and the next attempt will be much more convincing (if another attempt is possible, there is enough doubt of the vaccine campaigns and data just keeps piling up that vaccines are mostly bogus (there are some that work well, a limited number) that this type of approach may have to be scrapped all together...).

VACCINATION
- A brief essay by Herbert Spencer.

The text is copied from his last published work, Facts and Comments,
originally issued in 1902.

http://forums-cdn.appleinsider.com/1...t_Spencer.jpeg

The passage of time has served to emphasize the questions raised by the great English philosopher. Although compulsory vaccination still obtains in many quarters, and although laymen, even more than the medical fraternity, are avid for serumization against many other diseases -- still there is evident a rising tide of protest and even of alarm over the ascertained and suspected sequential dangers and damages from this source. The "miracle notion," once confined exclusively to theological and popular religion, has spread far and wide under other names into other fields -- nowhere more injuriously than in the vast domain of medicine.

"WHEN once you interfere with the order of Nature there is no knowing where the results will end," was the remark made in my presence by a distinguished biologist. There immediately escaped from him an expression of vexation at his lack of reticence, for he saw the various uses I might make of the admission.

Jenner and his disciples have assumed that when the vaccine virus has passed through a patient's system he is safe, or comparatively safe, against small-pox, and that there the matter ends. I will not here say anything for or against this assumption.(1) I merely propose to show that there the matter does not end. The interference with the order of Nature has various sequences other than that counted upon. Some have been made known.

A Parliamentary Return issued in 1880 (No. 392) shows that comparing the quinquennial periods 1847-1851 and 1874-1878 there was in the latter a diminution in the deaths from all causes of infants under one year old of 6,600 per million births per annum; while the mortality caused by eight specified diseases, either directly communicable or exacerbated by the effects of vaccination, increased from 20,524 to 41,353 per million births per annum -- more than double. It is clear that far more were killed by these other diseases than were saved from small-pox.(2)

To the communication of diseases thus demonstrated, must be added accompanying effects. It is held that the immunity produced by vaccination implies some change in the components of the body: a necessary assumption. But now if the substances composing the body, solid or liquid or both, have been so modified as to leave them no longer liable to small-pox, is the modification otherwise inoperative? Will any one dare to say that it produces no further effect than that of shielding the patient from a particular disease? You cannot change the constitution in relation to one invading agent and leave it unchanged in regard to all other invading agents. What must the change be? There are cases of unhealthy persons in whom a serious disease, as typhoid fever, is followed by improved health. But these are not normal cases; if they were, a healthy person would become more healthy by having a succession of diseases. Hence, as a constitution modified by vaccination is not made more able to resist perturbing influences in general, it must be made less able. Heat and cold and wet and atmospheric changes tend ever to disturb the balance, as do also various foods, excessive exertion, mental strain. We have no means of measuring alterations in resisting power, and hence they commonly pass unremarked. There are, however, evidences of a general relative debility. Measles is a severer disease than it used to be, and deaths from it are very numerous. Influenza yields proof. Sixty years ago, when at long intervals an epidemic occurred, it seized but few, was not severe, and left no serious sequelae; now it is permanently established, affects multitudes in extreme forms, and often leaves damaged constitutions. The disease is the same, but there is less ability to withstand it.

There are other significant facts. It is a familiar biological truth that the organs of sense and the teeth arise out of the dermal layer of the embryo. Hence abnormalities affect all of them: blue-eyed cats are deaf and hairless dogs have imperfect teeth. (Origin of Species, Chap. I.). The like holds of constitutional abnormalities caused by disease. Syphilis in its earlier stages is a skin-disease. When it is inherited the effects are malformation of teeth and in later years iritis (inflammation of the iris). Kindred relations hold with other skin-diseases: instance the fact that scarlet fever is often accompanied by loosening of the teeth, and the fact that with measles often go disorders, sometimes temporary, sometimes permanent, of both eyes and ears. May it not be thus with another skin-disease -- that which vaccination gives? If so, we have an explanation of the frightful degeneracy of teeth among young people in recent times; and we need not wonder at the prevalence of weak and defective eyes among them. Be these suggestions true or not, one thing is certain:-- the assumption that vaccination changes the constitution in relation to small-pox and does not otherwise change it is sheer folly.(3)

THREE (3) FOOTNOTES LISTED BELOW:

(1) Except, indeed by quoting the statement of a well-known man, Mr. Kegan Paul the publisher, respecting his own experience. In his Memories (pp. 260-1) he says, respecting his small-pox when adult, "I had had small-pox when a child, in spite of vaccination, and had been vaccinated but a short time before. I am the third of my own immediate family who have had small-pox twice, and with whom vaccination has always taken."
Back to text.

(2) This was in the days of arm-to-arm vaccination, when medical men were certain that other diseases (syphilis, for instance) could not be communicated through the vaccine virus. Any one who looks into the Transactions of the Epidemiological Society of some thirty years ago, will find that they were suddenly convinced to the contrary by a dreadful case of wholesale syphilization. In these days of calf-lymph vaccination such dangers are excluded: not that of bovine tuberculosis, however. But I name the fact as showing what amount of faith is to be placed in medical opinion.
Back to text.

(3) A high authority, Sir James Paget, in his Lectures (4th ed. p. 39) says:-- "After the vaccine and other infectious or inoculable diseases, it is, most probably, not the tissues alone, but the blood as much or more than they, in which the altered state is maintained; and in many cases it would seem that, whatever materials are added to the blood, the stamp once impressed by one of the specific diseases is retained." Here is a distinct admission, or rather assertion, that the constitution is changed. Is it changed for the better? If not, it must be changed for the worse.
Back to text.

Cross-Post from Another Thread

U.N. Predictive Programming
Vaccines & Depopulation Agenda 21

SCRIPTED GLOBAL CHAOS

https://youtube.com/watch?v=aEqoqA9XH_c

Published on Dec 12, 2014

- Go to Crystal Clark's website: http://drowninginabsurdity.org/
- Visuals from the U.N. World Population Prospects page called "Fertility Maps": http://esa.un.org/wpp/fertility_figu...ve-maps_TF.htm to listen to her latest interview with Time Monk Radio Network. Excerpt from that interview is found within this video.
- Special thanks goes to Mike Adams (Health Ranger) for follow-up report on the Kenya U.N. (WHO) Tenanus Vaccines found spike with infertility drug HCG making the vaccine essentially a Bio-Weapon that causes the mother's body to attack the unborn developing fetus.
- Also special thanks to Dr, Mahami of Nirobi, Kenya for his due diligence.
Music Track generated by Xendrius, "Demon Magicians" track - thank you for that.

- And a special 'NO THANKS' to Bill Gates for his role in the Agenda21 Depopulation Roll-out.

_________________________________

Scripted Global Chaos and
Other Unsustainable Reality Revisions

https://youtube.com/watch?v=1YAciYr54kE

TRANSCRIPTION of the EBOLA part of the Interview @ [1:45:00]

I would like listeners to really think about this, because this is an example of how psychic blocks are instituted with repetition & why we have to get out of the mind-set that repetition equals facts.

If people in their mind's eye... they've seen it enough times... if people will conjure of the image that they've used from day 1 with Ebola. And, if they will go back to their free Revision Knowledge Base & let their own mind tell them what they're looking at, they will know what it is... rather than what they've been told, repeatedly, what it is. And people have seen images of these creatures their entire lives, whether in grade school, learning about the life-cycle of a fly, as an adult looking at "how can I get healthier soil in my garden?"

http://livedoor.blogimg.jp/ogenre/im...3df41af2-s.jpg
What you're looking at is a photo of a worm... its not a virus

They keep saying its a virus. Well, the next logical question generally is: If there really is an Ebola virus, why are they showing a picture of a worm? Why don't they actually use the virus?

The problem with that is: There is no Ebola virus in nature. Ebola is a parasitic worm infection. And these parasites veraciously feed on the organs & the connective tissues of their victims, causing very painful & rapid death.

Now I began trying to explain this to people on social media, having foreknowledge that Ebola is a parasite, asking them, "Go look... go Google an image of the virus & then compare it to the worm. And then ask yourself, 'Why they don't look right?', 'Why they're not the same?'"

And the reason why I had to do that, is that I looked for days... I searched the internet for days to find just one pre-revision reference to Ebola as a parasite, and I couldn't find any. There is one I could give, but not at the moment. And I wasn't the one who found it... it was a discussion group, where somebody in another country did a search for an Ebola Parasite & found it. And to this day, a month later, its the only reference I have ever found.

So again, we have to ask ourselves, "how did we get to a point where you can convince billions of people that Ebola is a 'virus'? And on top of this, and this is where it gets very disturbing, is that we have report after report on television for a vaccine that's coming for a virus that does not exist. And furthermore, because Ebola is a parasite - its a worm parasite - you cannot vaccinate against a parasite. So, what will really be in the vaccine. And who will be asking these question?

If this happens 10 years from now... something like this happens 10 years from now, and there are no references left, people, or otherwise, to a pre-revision reality, how can we prove it?

Because, I know the first thing somebody is going to say to me, "Well show me the link." The people revising reality know that the first thing that someone's going to say... and so there aren't any... there aren't any left, its nearly impossible to find.

And there are some very interesting changes in the scientific language that happened before this revision. People might find it interesting to know, especially given the "Zombie" meme that is so prolific, is that in the beginning, pre-revision science considered viruses non-living biological contaminants, because they do not require a host to feed for sustenance & they cannot reproduce themselves using their own parts. Rather, a virus must, very much like a computer virus, hijack the code of a cell & replicate itself. So now you have the cell replicating the virus, rather than... you know... a copy of its own cell.

So this was changed. And part of the confusion... if you try to find... you can use the term, query the term 'Ebola parasite' and in all the links that you will get, you will see that phrase, but when you inspect the articles upon opening the link, you will find its been replaced with 'virus'. And what makes it worse was a reclassification of viruses as parasites, because of subtle changes in the definition. The attachment... the 'need to be attached' for a parasite was removed, and 'shelter' was added.

So, now we have a definition of parasite that states that 'anything that uses another living thing for shelter, or requires it for sustenance' is now a parasite. And this revision includes humans. Now we are parasites.

And so this goes back to this same mind-set, its a very, very twisted mind-set. This people are eugenic fanatics. And so at this point, we have to really heavily consider...

When we look at vaccines, we see that people are being sterilized, we see the cognitive damage that is being done, we see the reproductive damage that's being done. And we see also military contractors are bidding on... in the U.K., for example, to control their health program, and here we have Obamacare that was pushed through. And you'll always find reality revisionism always avoids democratic processes. It doesn't want the scrutiny, it doesn't want the oversight & it doesn't want people voting on it. This is the way it works.

So when we look at this & we see, okay, 'Common Core' is literally teaching children to replace numbers with shapes. So 'a thousand' is now 'a cube'. And if the parents of children that are learning 'Common Core' try to teach their children the old way, which is a competing reality, and children use it in school, they're automatically 'failed'.

So at some point, when the parents die-off, we're going to have children that aren't going to know what '1,000' was, they're going to see 'cube', okay. This is the kind of dumbing-down that is happening. And this is what allows for something like an Ebola pandemic narrative to happen.

So what we really need to ourselves is: When people get these vaccines... I don't know if you guys are familiar with "fun-vacs" [video], do you remember that whole thing? Where they admitted that 'new battlefield' is the enemy's mind, okay. So, this is the "new battlefield" & they've identified the neural connections that create fundamentalist ideas, and people that believe in god & they were joking around about a vaccine that they called "Fun Vacs", because it could wire the brain. This again goes back to Transhumanism. Because, while we are not two separate species of humans, these things can make it true.

So, are vaccinations that are killing, maiming & disabling people, a method of eliminating the competition? I think it certainly fits the criteria.

_________________________________

From my own search: Dr. Michael Smith describes Ebola in saying this: "This worm-like virus..." Source

Image From Jon Rappaport Article
http://jonrappoport.files.wordpress....ng?w=510&h=233
Caption Reads: "A picture of the Ebola-virus worm-like thing"
SOURCE

The virus detective who discovered Ebola in 1976
http://news.bbcimg.co.uk/media/image...ntwerpcopy.jpg
Peter Piot: "We saw a gigantic worm like structure - gigantic by viral standards," says Piot. "It's a very unusual shape for a virus, only one other virus looked like that and that was the Marburg virus."

turiya