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EbolaGate is actually a Vaccine-inducement/Genetic Bioweapons False Flag attack strategy, with sophisticated alternative scenarios

VANCOUVER, BC –  EbolaGate is actually a Vaccine-inducement/Bioweapons False Flag attack strategy, with many sophisticated alternative scenarios, some of which may or may not materialize as in all false flags. The basic premise is to start an Ebola “outbreak”, followed by an inducement campaign to take vaccones that themseves are genetic bioweapons, in West African countries where local immune systems and health profiles are compromised, there are unsanitary conditions, little public health care, and martial law quarantines for mass infection can easily be imposed (as when towns of 50,000 persons are now being quarantined rather than the infected persons in the towns). Instead of being treated with known Vitamin C and immune system treatments, local populations are given ineffective treatments, or worse, treatments that are themselves bioweapons. The scenario here, led by WHO, is to covertly maximize infection rates and vector propagation, shred local health care and public order (nurses are now on strike in one country). This scenario is aimed at (1) creating a base for an African Bioweapons genocide, long sought because of the mineral, oil and gas wealth of Africa [Think of the US Rangers infecting of South Africa with the AIDS virus embedded in the small pox vaccine in the mid 1990s] (2) Providing the jumping-off point for mutation of the EbolaGate viruses and their traveling via air travel, sea travel, land, to Europe, India, Asia, and North and South America. In North America there awaits a sophisticated Ebola Gate False Flag machine led by WHO-CDC [Nazi-CIA] and Martial law regulations signed by George Bush I & II, Clinton, and Obama that can mandate FEMA incarceration and mass vaccinations with EbolaGate vaccines that maim or kill as part of the depopulation plan.

To see the estimated death toll, under current infection rates of Ebola gate by June 2016 of Infected persons: 4,707,573,324 [4.7 Billion] Dead persons: 2,877,739,573 [2.8 billion] please go to:

Regularly Updated! Deadly Ebola Virus Outbreak – EbolaGate


Alfred Webre: Plan A is Martial Law; Plan B is Ebola. Awareness and Critical Mass can deconstruct planned extermination

What The Hell Kind Of Vaccine Is That?

This generation of vaccines is not the vaccine people imagine in which a bit of antigen from some disease is injected into the person to stimulate antibodies.
Skipping over whether that ever worked or not, people might want to know the current vaccines are DNA vaccines.
They shoot patented genetically modified stuff into people, intended for “uptake” by the person’s DNA.  Skipping over whether once someone has patented material in them the corporations might claim ownership of organs or blood.  This is just what Monsanto does of crops in which their patented DNA shows up in farmers’ plants, even if by accident of wind and pollen, or caused to be there by Monsanto itself.
Whether a corporation which owns the patent on what is being injected into people’s children might make claims on that child’s body or not, people might want to stop and consider what the genetically modified stuff consists of in the first place.
They might especially want to do that since the genetically engineered material is specifically meant to alter their DNA, their body’s blue print.  (Would you let someone come in and alter the blue print of the house you are building without permission, and without seeing what’s in their plans?)
So, what’s in these DNA (GMO) vaccines?
There is SV 40 there, for a starter.  It causes cancer.  But it’s just a starter.

From Wikipedia on DNA vaccination:

Another consideration is the choice of promoter. The SV40promoter was conventionally used until research showed that vectors driven by the Rous Sarcoma Virus (RSV) promoter had much higher expression rates.[1] More recently, expression rates have been further increased by the use of the cytomegalovirus(CMV) immediate early promoter. Inclusion of the Mason-Pfizer monkey virus (MPV)-CTE with/without rev increased envelope expression. Furthermore the CTE+rev construct was significantly more immunogenic than CTE-alone vector. [16] Additional modifications to improve expression rates have included the insertion of enhancer sequences, synthetic introns, adenovirustripartite leader (TPL) sequences and modifications to the polyadenylation and transcriptional termination sequences.[1] An example of DNA vaccine plasmid is pVAC, it uses SV40 promoter.
SV 40 was in the polio vaccines in the 1950s.  It was banned in vaccines in 1961 because it causes tumors.  But they are still using it though it led to an epidemic of soft tissue cancers.

SV40 was the 40th virus found in rhesus monkey kidney cells when these cells were used to make the polio vaccine. This virus contaminated both the Inactivated Polio Vaccine (IPV) created by Dr. Jonas Salk and the Oral or “Live” Polio Vaccine (OPV) created by Dr. Albert Sabin.

Children being fed sugar cubes with the oral polio vaccine. Circa 1961.

In 1961, SV40 was discovered by Dr. Bernice Eddy of the National Institute of Health, Division of Biologics when she took the material used to grow polio vaccines and injected it into hamsters. Tumors grew in the hamsters. Her discovery was subsequently validated by Drs. Maurice Hilliman and Benjamin Sweet of Merck.

Upon the discovery that SV40 was an animal carcinogen that had found its way into the polio vaccines, a new federal law was passed in 1961 that required that no vaccines contain this virus. However, this law did not require that SV40 contaminated vaccines be thrown away or that the contaminated seed material (used to make all polio vaccines for the next four decades) be discarded. As a result, known SV40 contaminated vaccines were injected into children up until 1963. In addition, it has been alleged that there have been SV40-contaminated batches of oral polio vaccine administered to some children until the end of the 1990’s.

Rhesus Macaque (Macaca mulatta)
Poor monkey.  He didn’t make the polio vaccines.
And he didn’t get those cancer causing polio vaccines containing SV 40 mandated, either.

SV 40 was a problem.  But now there are new problems starting with but not limited to the rather astounding fact that most of vaccines now are DNA vaccines.  And DNA vaccines have never been approved in the US for human use.

How have the vaccine corporations been able to go forward with selling those vaccines?  How can the CDC urge parents to let their children be injected with vaccines unapproved in the US for use in humans?

But shocking as it is that the DNA vaccines (most of what’s on the market) have not been approved to be given to people, when one looks at what is included in these new DNA (GMO) vaccines, it’s hard not to think “Good God, are they out of their minds?”

So what else in these DNA (GMO) vaccines?

The Rous Sarcoma virus (RSV) is also there, being used as a promoter.  It’s quite a nasty cancer-causing virus, .just like SV 40, but maybe more so.  (Is a sarcoma – a connective tissue cancer – harder to treat that a soft tissue one?).

In 1911, Peyton Rous discovered that cancer could be induced in healthy chickens by injecting them with a cell-free extract of the tumor of a sick chicken.

He ground up samples of the tumor and passed the material through a filter with pores so fine that not even bacteria could get through. However, the tumor filtrate was able to induce cancer when injected into chickens.

This was the first demonstration of an oncogenic virus — that is, a virus capable of causing cancer. The tumor was a sarcoma, a tumor of connective tissue. The virus was named the Rous sarcoma virus (RSV).

The Rous sarcoma virus is a retrovirus (as is HIV, the virus that causes AIDS).

As soon as RSV infects a cell, its reverse transcriptase synthesizes DNA copies of its genome. These enter the nucleus of the cell and insert themselves randomly throughout the DNA of the host’s chromosomes.

Normal gene transcription within the nucleus now produces an RSV messenger RNA (mRNA) that reenters the cytoplasm. Some copies of this mRNA are then translated by the normal machinery (e.g., ribosomes) of the host cell into protein products. Other copies of the RNA become incorporated into new virus particles.

…. each end of the RNA molecule has a set of repeated sequences of nucleotides (“R” and “P”) that perform at least two important functions:

  • they enable the DNA copies of RSV to insert into the host’s DNA and
  • they act as enhancers, causing the host nucleus to transcribe the RSV genes at a rapid rate.

After looking at what RSV does to DNA, to say these DNA vaccines affect DNA seems a sizable understatement.  RSV gets into a person’s DNA where it then gets the person’s cell nuclei to reproduce RSV (a sarcoma – a cancer) and rapidly.

What else is in these DNA (GMO) vaccines – vaccines which have never been approved for human use in the US?

The DNA vaccines also use cytomegalovirus as a promoter.  And cytomegalovirus is associated with small heads (and many other severe problems) in babies (see below)r.

The CDC refers to “congenital” cytomegalovirus as CMV that is “present at birth.”  But DNA vaccines include CMV and logically they might pass this virus to pregnant women and then fetuses could become infected with it.  So for a baby to be born with a CMV infection doesn’t mean the CMV is “congenital.”  It could be vaccine-induced.  But it’s handy to refer to CMV as “congenital” CMV as that immediately distracts from the DNA vaccines (that are not approved for human use) containing it.  It also slips past the fact that these vaccines (and they would be DNA vaccines) are being incessantly pushed on pregnant women.  So, when a baby is born with a CMV infection, rather than asking what caused the CMV infection and perhaps see this DNA vaccine connection, a baby with the infection is simply considered to have a very unfortunate congenitalcondition.

From the CDC:

Most (90 of every 100) infants who are infected with cytomegalovirus (CMV) at birth (congenital CMV infection) appear healthy at birth. Health problems or disabilities due to congenital CMV infection may appear 2 or more years after birth, or they may never appear—80 of every 100 infants with congenital CMV infection never develop symptoms or disabilities.

Signs and Symptoms

Signs of CMV infection that may be present at birth

  • Premature birth
  • Liver problems
  • Lung problems
  • Spleen problems
  • Small size at birth
  • Small head size
  • Seizures

Permanent health problems or disabilities due to congenital CMV infection

  • Hearing loss
  • Vision loss
  • Mental disability
  • Small head size
  • Lack of coordination
  • Seizures
  • Death (in rare cases)

Children with congenital CMV infection are more likely to have permanent disabilities if they had symptoms of CMV infection at birth. However, some children with congenital CMV infection who appear healthy at birth can develop hearing or vision loss over time due to congenital CMV infection. For this reason, if you know your baby was born with CMV infection, it is important to have his or her hearing and vision tested regularly.

Prevention – pregnant women should very wary of babies and children.

These DNA vaccines don’t stop at SV 40 or RSV or CMV but also use the Mason-Pfizer monkey virus (MPV), having apparently not learned (or learned?) that simian viruses have been a disaster in vaccines (causing cancers and retroviruses like AIDS).  The DNA vaccines with this patented (to Pfizer) monkey virus are then actually coupled with CMV for even more effect – the same viral infection that can break down the mind, vision, hearing, lungs, liver and other organs of babies and children over time and even kill them.

And that’s leaving off all the “[a]dditional modifications to improve expression rates …. enhancer sequences, synthetic introns, adenovirus tripartite leader (TPL) sequences and modifications to the polyadenylation and transcriptional termination sequences.”  It’s way more than unclear what all this is, but “synthetic” introns are synthetic rather than real biology, that are meant to affect or become part of one’s DNA.
For most people, it looks for all the world like those making DNA vaccines have been injecting people with them before getting them approved for use by humans, and are using one monkey and cancer virus after another and magnifying their impact by adding in a viral infection that wrecks babies.
If two wrongs don’t make a right, can multiple cancer viruses and a viral infection that destroys children, make health?
Aren’t cancer viruses and viruses that cause babies to be born with small heads (or to die) a bit weird (dare one say unlikely?) as a method to prevent common and usually minor childhood diseases ?
And wouldn’t it make much more sense to just use vitamin C which is an absolute viricide and easily kills all the childhood disease viruses?  Why get fancy or cancer-y?
How does vitamin C kill viruses?   First, you take 3 cancer viruses and a synthetic rabbit’s foot …. just kidding.
The mechanism of action of high dose vitamin C is known and understood. In normal healthy tissues it acts as an antioxidant. In other tissues, it generates hydrogen peroxide, the chemical that platinum blondes use to bleach their hair. This happens in sick and inflamed tissues, for example in a malignant tumour. The process is typically a form of Fenton reaction, generating free radicals. The oxidation and free radicals arising from the hydrogen peroxide kill bacteria and inactivate viruses. In other words, vitamin C acts as a targeted bleach and antiseptic.
Just on the face of it, it seems a common sense thing to skip any technology that has never been proven as safe for humans.  And why not stick with something unequivocally safe and which cures all viruses, rather than accept just “promises” to prevent them (while we can see again and again, from all the childhood disease outbreaks in vaccinated kids, that the promises are just promises).
And, just on the face of it, it seems such a greatly sane thing to ALWAYS bypass shooting any, to say nothing of multiple, cancers and other viruses into pregnant women, babies, children and adults.  Actually, it seems reasonable to bypass shooting those things into anything living.
But some seem to very much like mixing together and experimenting with strange things and injecting it into people.  Here is a list of some of their known experiments.
Most people just want to be well and enjoy life.  They have accepted vaccines or have brought their children get them in order, they h0ped, to avoid the of risk their getting very sick and dying.  But with the new DNA vaccines including Simian Virus 40, Rous Sarcoma Virus, Mason-Pfizer monkey virus (MPV), and cytomegalovirus, and even mixed together, vaccines as a safety net to protect people from minor childhood disease and short-lived flu, appear on closer inspection, to be taking on a rather large risk of getting some of the worst diseases there are out there, or potentially even new combinations of them.
This vaccine situation starts to feel rather like what we’ve learned about food or shampoos.  When they include an endless list of things we can’t say or know nothing about, they just haven’t seemed to add up to anything good down the line.
If people are so concerned about viruses, why bother with the risk of cancer virus-loaded vaccines, when Vitamin C effectively kills all viruses?  Vitamin C doesn’t pose any risk of causing cancer or of slowly deconstructing children’s physiology over time.  Vitamin C’s side effects aren’t more diseases, but improved health in countless ways.

Given supplemental ascorbate (vitamin C), not merely from birth but also all throughout gestation, Klenner’s uniformly healthy, trouble-free infants were known by the staff as the “Vitamin C Babies.” (12)

In a 1978 letter to Klenner, Irwin Stone writes that he thinks that “giving levels of ascorbate for long periods of time at the daily levels you recommend. . . is equivalent to creating a new human subspecies, ‘Homo sapiens ascorbicus’ . . . with unusual resistance to disease and stress and with a prolonged life span.”

This article shows vitamin C is safe and highly effective.

The Origin of the 42-Year Stonewall of Vitamin C

And this one shows how it was squashed by exactly those who like experimenting on people and seem so oddly interested now in injecting cancer viruses into people.

EbolaGate is actually a Bioweapons False Flag attack strategy, with many sophisticated alternative scenarios

Ebola Turning Out to be Joint Bio & Psych Warfare Assault from George Soros & Bill & Melinda Gates

Ebola Turning Out to be Joint Bio & Psych Warfare Assault from George Soros & Bill & Melinda Gates
By Ishtar Babilu Dingir


In the wake of the latest terror scam, Ebola, President Barack Obama has just signed an executive order to enable the enforced detention of people with severe respiratory disease. Yes, you heard that right. Not Ebola. Just people with breathing problems.

However, the only known strain of Ebola to be transmitted by airborne droplets – Mayinga – hasn’t been seen since 1978.

It reminds me of a similar sleight of hand, when our warmongering leaders started banging the war drums against Iraq over 9/11, while insisting that the perpetrators of the twin towers attack were from a cave in Afghanistan.

But if you are worried about Ebola, please don’t be. It’s beginning to seem as if it’s just more psychological warfare from the usual suspects … just like Bird Flu and Swine Flu.

It’s another case of ‘figures lie, and liars figure’.

If you’re talking possible worldwide epidemic, the stats coming out from the World Health Organisation (WHO) don’t quite hang together as Ebola is not even at anything like epidemic proportions in Africa. Added to which, the genesis of Ebola seems to have come from a nucleus which has, at its centre, a bioweapons lab owned by multi billionaires George Soros and Bill and Melinda Gates.

Even according to WHO figures, the spread of Ebola in Africa is as nothing as compared to the amount of people who die in the West of ordinary common-or-garden influenza every year. You’re looking at a total of 456 deaths overall, for Ebola, against an annual figure of deaths from influenza of 250,000 and 500,000. Both these figures come from WHO health reports, and do remember the Ebola figure of 458 is overall, whereas the flu figures are yearly.

So hopefully that enables us to gain a saner perspective on the Ebola War of Terror tactic than the one being trumped up by the mainstream media which seems to be well onboard with this psychological warfare operation.

As Jon Rappoport, in an article for Infowars, says:

“Ebola is a propaganda operation. Choices are being made: what to emphasize, what to ignore, what to use in order to invoke fear. Producing fear, one way or another, is a standard element in exerting top-down control over the population. When people are afraid, they’re compliant, they’re obedient to authority. And that’s the agenda.”

The propaganda side of the operation is being diligently adhered to by WHO head Margaret Chan. When she addressed a summit of regional leaders the other day, her figures conflicted with actual reported figures by WHO in their July 25 update, “Ebola Virus Disease, West Africa”. She told the summit that the virus has claimed 728 lives in Guinea, Liberia and Sierra Leone since February…. almost twice as many as the offical figures record.

Chan also told them that Ebola kills up to 90 per cent of those infected when from the same report, we can see that the 456 deaths were from a total of 814 infected… so that’s almost half.

It really does pay to go the actual reports rather than rely on the words of spokespeople, because more often than not, they’re on the gravy train.

So with these differing figures, we can see that those steering the agenda have not quite got their ducks in a row yet. This helps us to read between the lines.

There was a very revealing comment from a pharmacist over the weekend, who obviously hasn’t yet got the memo. In an interview with Bloomberg News, Dr, Ben Neuman admitted that there isn’t enough “panic” surrounding the Ebola virus for the pharmaceutical industry to justify developing a cure.

“It’s not just one drug that we need for Ebola, we need a cocktail of drugs and perhaps a nice vaccine that could be used, these all take a lot of money and right now in the history of what we know at least there have been [so few infected.]

“It sounds scary but I don’t know if there’s enough panic or enough people who are potential customers for these drugs to warrant a company, a private company, putting the money in it would take to develop these.”

Actually, the Monsanto-owned Tekmira Pharmaceuticals did develop an Ebola vaccine, which was tested on humans with positive results. However, it was put on hold by the (Monsanto dominated) FDA, and this led to doctors to create a petition insisting that the ban should be lifted.

Apparently, shares in Tekmira rose sharply on Friday on news that the Ebola outbreak in West Africa has intensified, as investors expect the vaccine to be reconsidered and released.

Oh what a tangled web they weave!

So where is Ebola coming from?

The US Centers for Disease Control (CDC) tells us that the virus is spreading because of unhygenic practices in African hospitals. So it can’t be a coincidence that a bio-warfare lab in a Sierra Leone hospital, with a list of investors that reads like a Who’s Who of the New World Order, including known eugenicists George Soros and Bill and Melinda Gates, is at the centre of the Ebola outbreak in Africa. These are the richest people in the world and they own our governments.

Kenema Government Hospital in Sierra Leone, which has been at the eye of the Ebola storm, houses a US biosecurity level 2 bioweapons research lab with links to the Bill and Melinda Gates Foundation and Soros Foundation. There, US biodefence scientists have been working on viral fevers such as Ebola for decades.

The locals certainly believe that Kenema Lab in Sierra Leone is the cause of the outbreak of Ebola there. Bloomberg reports how locals threw stones at the hospital and the police station, amidst fears that health workers were using Ebola as a ruse to kill people and collect body parts.

The fears were sparked by a ‘rumour’ apparently started by a nurse who worked there, who the lab quickly insisted was mentally ill. This is a common and classic tactic, to discredit the whistleblower. You have to wonder how a mentally ill person was considered fit to work in such a sensitive and dangerous facility. But of course, she probably was completely sane, and just fearless enough to tell the truth.

It’s a matter of public record that this biowarfare lab has been working on developing various strains of Ebola for more than 40 years, which begs the question, how on earth would they expect to control it in a battleground situation? I think the answer to that is they couldn’t, and that weaponised Ebola is not and was never intended to be used just on the enemies’ troops, but on the ordinary civilians too. The Geneva Convention must be turning in its grave.

According to American Kabuki, who has researched this subject more deeply, this Soros/Gates lab has, so far, been unable to develop a strain of Ebola that will be virulent enough, and certainly not one which will spread in cooler climes than are found in Africa.

He says:

“They’ve been trying to weaponize Ebola for over 40 years. They can’t do it because the Mayinga strain of Ebola (the only known strain to be contagious through aerosol transmission) kills people too quickly for it to work as a broad spread bio weapon.

“They’ve been playing with the Marlburg/Ebola crosses to create a virus with a longer gestational period, so that cross infection/contamination will spread farther. but Marlburg cancels out the aerosol transmission factors of the Mayinga strain of Ebola, which leaves them with oral/mucous membrane transmission, which isn’t effective as the virus dies very quickly unless it’s in a very hot humid climate (hence the fact that they do their testing in western Africa in jungle climates). Air conditioning kills the virus almost instantly.

“So Ebola has only ONE strain that is suspected to have been transmitted by aerosol exposure to the live virus. The Ebola Zaire strain called “Mayinga” (named after the nurse, Mayinga, who died after being infected with the virus without any known method of transmission- meaning that they suspect that she died through an aerosol transmission, as in: micro particles that are actually in the air, and transmitted through contact with the virus ONLY by air, ie: inhaling it), although it has never been proven that she contracted the virus though aerosol contamination.

“The Zaire Mayinga strain is the only Ebola strain that has ever been even suspected of being transmitted through aerosol contamination, and it is extremely rare. To the best of my knowledge, the Mayinga strain hasn’t been seen in an outbreak since 1978.”

Meanwhile, this Sierra Leone lab is being quickly shut down, and thus avoiding any inconvenient police investigation.

Multi-billionaire George Soros, a friend of Sierra Leone’s president, is also a huge investor in the so-called “Ebola triangle” of Sierra Leone, Liberia and Guinea.

So they probably figured this: the Ebola terror scam might work well as a psy-ops for three reasons – Ebola is a foreign disease from exotic lands, the symptoms are bloody and grisly and it can also be deadly. This means that Ebola may stand a better chance of capturing the imagination of a public pre-programmed by Hollywood on horror movies, where the information war is largely being waged.

At the end of the day, it’s all about ‘follow the money’, and a dumbed down and scared population who won’t question your lies to raise your share price.

Conclusion: World War III will not be conducted between nations but by a eugenistic and psychopathic global elite on the ordinary people, largely through bioweapons and psychological warfare.

We can see this writ large with Ebola.


Ebola, Swine Flu, Zika, SARS – The Anatomy of a False Flag Disease

4 thoughts on “EbolaGate is actually a Vaccine-inducement/Genetic Bioweapons False Flag attack strategy, with sophisticated alternative scenarios

  1. No reflection on crazzfiles
    EBOLA vaccine will most likely made up of a cheap dishwashing liquid.
    GSK … is broke.
    GSK … in deep legal trouble – lawsuits are coming at them from every direction.
    GSK … abandoned everything & ran for their lives from India.
    GSK … such is the sentiment towards GSK it is a wonder that their bulidings of opperation have not been burned to the growned.
    GSK … genetically is not possible – it is another lie.

  2. I have always been a bit of a fan of Michael Douglas – and isn’t he fantastic as SOROS .. If it can ever be told, Michael deserves an award for pulling it off.

  3. 30 seconds into the video – look at him laying about in the dirt playing the fool with a nice clean white & lime green TShirt on. Obviously he dosen’t give a hoot that his mother washes by hand, in a crude laundry facility.

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