The Ebola Outbreak: The "Pandemic" that isn't.
There have been many many moments over the past few years that have made me ponder my past and the experiences and knowledge that I have gathered along the way. I cannot tell you how many times in the last two years alone that I have had major personal revelations about things that I have gone through or learned in the past that are suddenly so relevant in the NOW. Last night was one of those moments.
For almost 20 years I have had an almost morbid facination with the Ebola virus, and Haemoragic fevers such as Marlburg and Lassa, in general. It started when I read the book "The Hot Zone" in 1996, and continued when I worked with a former US Special Forces Military doctor in Thailand who had a vast amount of knowledge on the ebola virus. Ever since then I have read possibly hundreds of medical reports and studies on the topic.... reports and studies that were written before this so called "outbreak" and the very blatant editing that has been perpetrated across the media.
..... obviously to prepare myself for this article today.
.... Very interesting that the Wikipedia listing for Ebola Zaire doesn't specify how the virus is transmitted, don't you think?
If you've read any main stream media news outlet or alternative news site, you've heard all the panicked fear mongering about the purported "Ebola" outbreak in west/central Africa. These reports started appearing in the main stream media news in February 2014 while I was in Malta. I immediately started following the news and kept abreast of the latest developments. I also immediately started to smell a rat. The Media banged on the fear porn drum for a few weeks and then it all just sorta disappeared (they couldn't seem to keep people's attention on "world war III" starting in the Ukraine AND the "pandemic of Ebola" at the same time). Then in the past few weeks they've ramped up the Ebola fear porn drama again.....
.... Distract Distract Distract.
Ukraine didn't work out the way they wanted so they needed another distraction. Enter the insanity of Netanyahu and the debacle being played out in the gaza strip. But now that is not working out for them either as the world is standing up and shining the light of outrage on Gaza. So another distraction is necessary. Enter: ebola panicked "pandemic" in africa.
I am not going to get into all the main stream media ebola circus- open any news website and you can read it all- but I will discuss several glaring pieces of obvious bullshit, and "facts" that the so called medical professional associations have invented to perpetuate this travesty.
"Their" goal is only one thing: FEAR & DISTRACTION. They need to keep the public distracted from the fact that their entire financial world empire has crumbled to the ground and they have lost everything they have. .... I'll be going into details on this subject in my next article. For this moment I will focus on the fear porn campaign that "they" are currently pushing onto the public.
Before I start posting the links and my commentary, I will post this note that I wrote in one of my skype rooms as an intro to the topic:
D.breakingthesilence: "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 cancells 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."
The first article I will post here is to show the vast amount of disinfo that is being spread by official "government" agencies about the Ebola virus. This article by Mike from Natural News shows the dangers of assuming that these "official" agencies are telling the truth. (Which I find strange as I know that Mike is usually not fooled by these type of things).
Ebola transmission by aerosols confirmed: virus survives for days outside infected hosts
Friday, August 01, 2014
Learn more: http://www.naturalnews.com/046276_Ebola_aerosol_transmission_infectious_disease.html#ixzz39FOxeNiE
(NaturalNews) Today Kurt Nimmo from Infowars.com is incorrectly reporting that "aerosol transmission is not possible" with Ebola. (2) That statement is part of an article entitled, "Don't Fear Ebola, Fear the State" which is, overall, a very compelling article.
Nimmo is a fantastic writer and a great researcher, but in this case his statement is factually incorrect and probably needs to be addressed. As clearly explained by the Public Health Agency of Canada: (3)
"INFECTIOUS DOSE: 1 - 10 aerosolized organisms are sufficient to cause infection in humans."
Ebola, you see, can "ride" on aerosolized particles of blood, mucous and other body fluids. Someone sneezing, for example, can cause Ebola viruses to be aerosolized where they land on other people's hands or faces. It only takes one virus entering the corner of your eye (or the corner of your mouth) to set off a full-blown infection......\
.....Even worse, Ebola is a strong survivor outside a host. Here's what the Public Health Agency of Canada says:
SURVIVAL OUTSIDE HOST: The virus can survive in liquid or dried material for a number of days. Infectivity is found to be stable at room temperature or at 4 C for several days, and indefinitely stable at -70 C. Infectivity can be preserved by lyophilisation....
Both of these statements by the Canadian "government" are incorrect and appallingly shine a light on the fact that the real FACTS about Ebola is being covered up, changed and re-written.
let me give you some hard core facts about Ebola:
Ebola has only ONE strain that is suspected to of been transmitted by aerosol exposure to the live virus. This is an absolute FACT. 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), but 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.
ALL the strains of Ebola, and Marburg viruses are very very contagious through membrane transmission- ie: through direct contact with liquid particles (blood, mucous, semen, sweat, urine) onto mucous membranes or through open wounds. This means that if you physically come into contact with liquid particles infected with an Ebola virus through your mouth, eyes, nose, genitalia or an open wound, then you have a very large probability of being infected with the virus. Hence: it is highly contagious though PHYSICAL contact with the infected bodily liquids of someone who has the virus. ie: though touching the body/body fluids, contact with the sheets, bandages, needles, medical instruments etc of an infected person.
BUT..... the virus doesn't not live very long outside of a human or animal host. ALL Hemorrhagic fever viruses (all strains of Ebola, Marburgs etc...) are actually very fragile virus particles that need a very specific environment to survive for even a short time. THIS is why all cases of Ebola always happen in the same place, in Central/West African jungles: HOT HOT HOT and WET WET WET. ALL Hemorrhagic viruses require extreme heat and humidity to survive, and as I said above, they literally die very quickly when they are exposed to air conditioning.
These are two of the main reasons that "they" were not able to weaponize Ebola before: because it requires direct contact with infected bodily fluids AND it dies very quickly when it comes in contact with drier, cooler air.
One of the other reasons that they were not able to weaponize Ebola is because it kills too quickly and the gestational period is too short for it to spread very far. Ebola Zaire has the highest mortality rate- close to 90% of those infected die from the virus, but it also has the shortest gestational period and it can be symptomatic as quickly as 2-6 days after contamination. As the onset of symptoms is so severe immediately, infected people are not likely to be boarding airplanes, going to night clubs or partaking in unprotected sex.
Marlburg virus is another form of Hemorrhagic fever that "they" have played with, but while it has a longer gestational period- close to 2-3 weeks- it also has a much lower mortality rate that varies wildly between 20-80%.....
The tampering of these viruses needed to make them a viable bio weapon is something they've been "working on" for at least 40 years.
..... And here is the proof of "their" work:
Human Ebola Virus Species and Compositions and Methods Thereof
US 20120251502 A1\
||Oct 4, 2012
||Oct 26, 2009
||Oct 24, 2008
|Also published as
||CA2741523A1, EP2350270A2, EP2350270A4, WO2010048615A2, WO2010048615A3
||Jonathan S. Towner, Stuart T. Nichol, James A. Comer, Thomas G. Ksiazek, Pierre E. Rollin
||The Government of the US as Represented by the Secretary of the Dept. of health
||BiBTeX, EndNote, RefMan
|Patent Citations (2), Non-Patent Citations (8), Classifications (39), Legal Events (1)
|External Links: USPTO, USPTO Assignment, Espacenet
All of the information that is contained in this patent is important and worth reading, even though the information is difficult to wade though unless you have some understanding of medical terminology that is used in these type of documents. It's also a lesson on reading what they are actually saying in amongst the mumbo jumbo. I've highlighted a few sentences that are very telling from a small excerpt of the document.
In another aspect, the invention provides vaccine preparations, comprising the inventive hEbola virus, including recombinant and chimeric forms of the virus, nucleic acid molecules comprised by the virus, or protein subunits of the virus. The invention also provides a vaccine formulation comprising a therapeutically or prophylactically effective amount of the inventive hEbola virus described above, and a pharmaceutically acceptable carrier. In one embodiment, the invention provides a vaccine formulation comprising a therapeutically or prophylactically effective amount of a protein extract of the inventive hEbola virus described above, or a subunit thereof; and a pharmaceutically acceptable carrier.\....\
... According to the present invention, the chimeric viruses are encoded by the viral vectors of the invention which further comprise a heterologous nucleotide sequence. In accordance with the present invention a chimeric virus is encoded by a viral vector that may or may not include nucleic acids that are non-native to the viral genome. In accordance with the invention a chimeric virus is encoded by a viral vector to which heterologous nucleotide sequences have been added, inserted or substituted for native or non-native sequences. In accordance with the present invention, the chimeric virus may be encoded by nucleotide sequences derived from different species or variants of hEbola virus. In particular, the chimeric virus is encoded by nucleotide sequences that encode antigenic polypeptides derived from different species or variants of hEbola virus."
noun: chimera; plural noun: chimeras; noun: chimaera; plural noun: chimaeras; noun: Chimera
(in Greek mythology) a fire-breathing female monster with a lion's head, a goat's body, and a serpent's tail.
any mythical animal with parts taken from various animals.
a thing that is hoped or wished for but in fact is illusory or impossible to achieve.
"the economic sovereignty you claim to defend is a chimera"
The Chimera was, according to Greek mythology, a monstrous fire-breathing hybrid creature of Lycia in Asia Minor, composed of the parts of three animals – a lion, a snake and a goat. Wikipedia\
"They" go to great lengths to create the illusion that this patent is for the creation of a vaccine to protect against Ebola... but you can't create a vaccine for a virus unless it is for THAT SPECIFIC VIRUS. Plain english: You have to create the "chimeric" virus in order for the "chimeric" virus based vaccine to work!! This means that if they are creating a vaccine from multiple viruses, the vaccine will only work for that CREATED virus. This is the ongoing mythology of the yearly flu vaccine: they create a vaccine that will only work on 2 or 3 strains of "flu" virus, but unless they know exactly which strain of flu is going to "appear" that year, the vaccine is completely useless! There are literally thousands of strains of the "flu" virus, hence unless they know exactly which one is going to be let loose in the public, they cannot produce a vaccine that has any ability to do anything (.... except spread the virus further though live virus vaccines of course).
This Patent is for a man made form of Ebola- one that has been created by combining several other viruses. I won't post it all here as it would make this article incredibly long, but if you'd like to do some homework, do a google search on the names and previous work of the inventors of this hybrid chimeric virus, and check out their other areas of study and research (polio and the common cold? hmmmmm).
Next up to research: who is running the patent. Who is buying up the license to distribute the virus or the vaccine? (did you know that Rumsfeld is the global license holder for the H1N1 vaccine?) and who are the agents (usually a law firm) for the patents? In Canada it is Ridout & Maybee LLP...... seriously? ..... And also look for any private offerings (investment offerings) by those agents that would enable funding the $800 billion to $1 trillion FDA bribe...I mean "price tag"...I mean "application and processing fees"...tee hee...and the subsequent "derivative market"/exchange traded fund to pay back all those sucker "institutional investors" who shove off the liabilities to the secondary markets and the public investors on main street...... bwuhaaaahaaaaahaaaaa!!! Wait!!!!!! No worries, the "investors" are still busy trying to figure out how to process the gold, silver, and metals molestation with Basel III promising a "new gold-backed financial system"....toooo much fun!!!!!!!! Hollywood seriously can't write stories like this!.... that last bit was written by Heather, who hijacked my computer for a few moments.
This Ebola "pandemic" that is purportedly happening in 4 countries in Africa - 3 of which have never had an outbreak of Ebola before: Liberia, Guinea and Sierra Leone- is very blatantly NOT acting like Ebola outbreaks usually do. First off, considering the "infected" numbers that were given in Feb 2014 at the beginning of this "outbreak", and the supposed spread of the virus to 3 other countries.... not enough people have died. I know that that is a morbid thing to say, but the Ebola virus kills very quickly, with a high mortality rate and IF the virus was in large city centres as the media is saying, and IF the virus was being spread through aerosol transmission as the media is saying, and IF the virus is getting onto airplanes and getting to Canada and the US and Europe as the media was saying was happening in late February 2014.... then WAY WAY WAY more people should of already have died from this "pandemic".
The World Health Organization has released statistics that Prove that the media is hyping up the fear porn. See the Jon Rappoport article quoted below....... the numbers do NOT add up. Not even slightly.
A few more interesting facts about this Ebola outbreak:
Initial outbreak in Guinea
In February 2014, the first Ebola virus outbreak registered in the region occurred in Guinea. By 23 April, the total number of suspected and confirmed cases in the Ebola virus disease (EVD) outbreak had increased to 242, including 142 deaths at a fatality rate of 59%. Originally, the suspected cases were reported in Conakry (four cases), Guéckédougou (four), Macenta (one) and Dabola (one) prefectures. On 25 March the Ministry of Health of Guinea reported that four southeastern districts—Guekedou, Macenta, Nzerekore, and Kissidougou—were affected with an outbreak of Ebola virus disease. The following day the Pasteur Institute in Lyon, France confirmed the Ebola strain as Zaire ebolavirus. An initial report suggested that it was a new strain of ebolavirus, but this was refuted by later studies which placed it within the lineage of the Zaire strain.\
Diagnostic methods for IDing Ebola in those 3 countries are uncertain. Therefore, we should only consider the category labeled “confirmed,” and even then we should have doubts.
So let’s look at the total for confirmed Ebola case numbers in those countries.
Confirmed number of deaths? 456.
Now consider another WHO report. This one is titled: “Influenza (Seasonal) World Health Organization,” dated April 2009.
It’s the WHO fact sheet on regular seasonal flu, the kind that is said to infect people globally, year after year, like clockwork.
Annual number of severe cases: 3-5 million.
Annual number of deaths: between 250,000 and 500,000.
Remember, that’s every year—not a one-time shot.
Tekmira Pharmaceuticals Corporation (TKMR) (TKM.TO), a leading developer of RNA interference (RNAi) therapeutics, announced today that it has received a $1.5 million milestone payment from Monsanto following completion of specified program developments.
About TKM-Ebola, an Anti-Ebola Virus RNAi Therapeutic
TKM-Ebola, an anti-Ebola virus RNAi therapeutic, is being developed under a $140 million contract with the U.S. Department of Defense's Medical Countermeasure Systems BioDefense Therapeutics (MCS-BDTX) Joint Product Management Office. Earlier preclinical studies were published in the medical journal The Lancet and demonstrated that when siRNA targeting the Ebola virus and delivered by Tekmira's LNP technology were used to treat previously infected non-human primates, the result was 100 percent protection from an otherwise lethal dose of Zaire Ebola virus (Geisbert et al., The Lancet, Vol 375, May 29, 2010). In March 2014, Tekmira was granted a Fast Track designation from the U.S. Food and Drug Administration for the development of TKM-Ebola.
What we are seeing is a man made virus being used (luckily not very successfully when you consider the virus they are working with) on an unsuspecting population as a means to drive the public into a fear spiral of desperation, to allow them to promote "their" martial law scam (you know... the one that hasn't worked for them yet?), and to create a vaccine hysteria to create the illusion of money being in circulation and strengthen the seriously lagging reputation of the worlds main medical institutions and agencies. This is a DISTRACTION.
D I S T R A C T I O N
DO NOT BE DISTRACTED BY THE SHADOWS.
Final word on Viruses in general: Do you know how many Viruses modern science and medicine has been able to cure?
Do you know how many Viruses have been eradicated with medicines or vaccines?
Yet.... we are all still here.
[Colour fonts and bolding added.].