Covid Is Fiction

international | anti-war / imperialism | opinion/analysis Tuesday June 01, 2021 21:03 by TEK

The Con-Vid Coup

There is no "covid" and fink lawrence is its propheteer. This article outlines 11 reasons why this is so.

March 7, 2020 - May 31, 2021

ICHAPTER 1 : NO DEATH SPIKES IN ITALY ! p.1

CHAPTER 2 : A CRIMINAL MASTERPLAN p.3

CHAPTER 3 : GLOBAL POLICE STATE p.3

CHAPTER 4 : VAXIS OF EVIL p.3

CHAPTER 5 : HUNTED DOWN SPIED ON TRANSHUMANIZED p.5

CHAPTER 6 : NO VIRUS NO DISEASE NO PANDEMIC p.6

CHAPTER 7 : TESTING THE TESTS p.9

CHAPTER 8 : ANTIBODY TESTING AND THERAPY, ANTIGEN

TESTS, LAMP TESTS : COMMERCIAL FRAUD p.32

CHAPTER 9 : THE VIRUS-SEQUENCING LIE p.37

CHAPTER 10 : SAY NO TO THIS VAXIS OF EVIL !!! p.43

CHAPTER 11 : (UN)TIMELY DEATHS p.58

CHAPTER 1 : NO DEATH SPIKES IN

ITALY !

MSM stated in May 2020 that there had been death spikes in Italy. There had not. It´s a huge lie spread by the national statistics center, directed by a fascist idiot with no mathematical competence whatsoever.

https://www.corriere.it/cronache/20_maggio_04/rapporto-istat-8fd5bbb4-8e05-11ea-b08e-d2743999949b.shtml?refresh_ce-cp

https://www.epicentro.iss.it/coronavirus/pdf/Rapporto_Istat_ISS.pdf

Read please, the Nota metodologica towards the end :

1. normally it takes ISTAT 10 months after the end of any given year to come up with definitive statistical death data : this year for the first time in history, they have been allowed to spread death data in near-real time - a physical and mathematical impossibility.

2. Allowing for this miracle for a moment, which makes no sense because local county offices are extremely slow here in reporting definitive data, as families take ages to communicate a death to them, and they themselves take ages to process the data and send it to Rome ; but anyway : out of 7904 counties in total in Italy, ISTAT has arbitrarily chosen only 6866 for their extrapolations, ELIMINATING FROM THE COUNT AS MANY AS 1038 COUNTIES WHERE THERE HAD BEEN A DECREMENT IN DEATHS !!! THAT is how they came up with the OVERALL spikes - by way of fraud !!! And also the local spikes at this point are extremely dubiously arrived at.

3. They state clearly that their provisory data HAS NO STATISTICAL VALUE WHATSOEVER, pending further future elaboration and checks !

So do not fall into the trap of believing in data accuracy when in fact those alleged spikes are the same type of lie as with PCR tests etc., that we shall demonstrate below.

Updating this chapter on February 4, 2021, I do consider plausible that there have been death increases in Italy and worldwide in 2020 - but certainly not due to the nonexistent covid as we shall see, instead to the fact that many people with potentially lethal diseases postponed their treatments out of fear of catching "covid" in hospitals, resulting in their deaths. Not to mention the endless suicides of impoverished people who were forbidden from working by criminal governments, or died from hardship and stress. And from lethal therapies and intubations administered after false "covid" diagnoses based on fraudulent testing as we shall see. And from being isolated in hospitals without assistance from loved ones.

Again : the dead passed off as "covid" deaths have been dying from 3 causes :

1. ordinary lethal pathologies such as interstitial pneumonia or severe flu complications, repackaged as the nonexistent covid on the basis of fraudulent testing ;

2. fear of going to hospital or treatment postponement for people suffering from lethal diseases such as cancer and cardiopathies needing constant hospital care ;

3. absurdly lethal therapies administered on the basis of frudulent covid testing over things like a little fever or a cold : once misdiagnosed, these poor people have been given stuff such as intravenous interpheron, tocilizumab, intubation/ventilation - to which many fragile people, especially elderly, have succumbed.

CHAPTER 2 : A CRIMINAL MASTERPLAN

https://off-guardian.org/2020/05/22/report-eu-planning-vaccination-passport-since-2018/

http:.//www.centerforhealthsecurity.org/event201/recommendations.html

https://futurism.com/neoscope/recent-simulation-coronavirus-killed-65-million-people

NOVEMBER 2019 : GATES GIVES A GOOD INVESTMENT TIP TO HIS COHORT RAY DALIO OF BRIDGEWATER FUND, WHO PROCEEDS TO MAKE A HUGE SHORT-TERM SPECULATIVE INVESTMENT BASED ON PREDICTING A STOCK EXCHANGE CRASH FOR MARCH 2020 - JUST WHAT WOULD REALLY HAPPEN THEN DUE TO THE FAKE "COVID" PANDEMIA :

http://www.lavocedellevoci.it/2020/03/16/pandemia-a-novembre-la-scommessa-da-1-miliardo-di-dollari-del-fondo-bridgewater/

https://en.wikipedia.org/wiki/Bridgewater_Associates

Remember how larry silverstein bought an insurance with lloyds covering terrorist attacks on his twin towers just before 911 ? Insider info it would appear.

Capitalfascism can only function through the spreading of fear and terror : until roughly 2001, they massmurdered their own, like 911 or the Bologna station massacre in 1980 ; starting with the Sandy Hook school shooting hoax back in 2012, they changed of tack and have started using their total control of the massmedia, to make humanity believe in false shooters, nonexistent islamist kamikazes, virtual neonazi attackers and the like - until now : the new fake enemy is a fake disease called "covid 19" (dress rehearsals for this new form of psyop had been sars end mers starting in 2003 - caused by viruses whose very existence is every bit as questionable as that of "sars-cov-2").

CHAPTER 3 : GLOBAL POLICE STATE

" Police and public health officials to have powers to detain people who may be infected

Kate Proctor

Police, public health and immigration officers will be able to detain people suspected of having coronavirus under new emergency powers rolled out by the government.

The new guidance would allow the officials to return people to where they have been asked to stay during the virus outbreak, believed to be in a bid to curb people leaving hospital early. They will also have the power to take people to screening and testing facilities.

The bill says: “These measures look to fill existing gaps in powers to ensure the screening and isolation of people who may be infected or contaminated with the virus and to ensure that constables can enforce health protection measures where necessary.”

THIS AMOUNTS TO FULL GESTAPOIZATION OF SOCIETY - NOT EVEN HITLER WENT THIS FAR WITH HIS OWN CITIZENS !!!!!!:

https://www.theguardian.com/politics/live/2020/mar/19/uk-coronavirus-live-boris-johnson-london-lockdown-williamson-refuses-to-rule-out-government-putting-london-in-lockdown-by-wee...9658f

CHAPTER 4 : VAXIS OF EVIL

How could pharma gangsters announce as early as of March 2020, they already had both drug and vaccine against "covid 19" at the ready ? It normally takes years to develop new drugs and vaccines against a new disease - no guaranteed achievement to boot. It is therefore mathematically certain that these same firms who are now claiming to have made drug and vaccine in 2 months, are those responsible for masterminding the "covid" hoax in the first place. They are going to sell governments snake oil - or worse, mandatory vax for all humanity. Some fear that, under the pretext of "covid", they are going to push a mandatory bar-code tattoo for all humanity. These vaxes they have been injecting into ignorant brainwashed masses for months now (as of Febr.6, 2021) are experimental mRNA vaccines that manipulate our genomic functions : they contain synthetic, chemical messenger RNA with instructions for our DNA to produce the alleged Spike protein of the alleged sars cov 2 virus : that is, they´ll coerce our bodies to first get sick in a sort of auto-immune way, only to then stimulate antibody reaction and immunitary memory - all of which over a nonexistent virus : they do not have it, nobody does, it´s never been isolated as we shall see below.

The sequence of this alleged S protein we are supposed to produce once vaccinated, is secret !! Unverifiable !! They haven´t even tried to come up with a traditional vax based on attenuated virus, because they do not have this nonexistent sars cov 2 virus !! Their real purposes are, on the one hand, to use humanity (bar themselves, the pig pharm owners and their political lackeys) as guinea pigs for a nazi experiment on how to turn us all into salvish GMOs ; on the other, to make trillions in de facto mandatory vaccines ( they say the vax is voluntary only to keep up fake hypocritical democratic appearances, but if u don´t take the vax, be sure they are going to blacklist you as they ´ve done in spain, or fire you from your job, etc. : blackmail, de facto vax coercion). More on this below. DO NOT TAKE THIS JAB !!!!

What are these firms so apparently able to develop drugs and vaccines at the speed of light ?

The first one is Moderna :

https://www.corriere.it/economia/finanza/20_febbraio_25/coronavirus-vaccino-arrivo-usa-pronti-test-sull-uomo-f76b58b8-579d-11ea-a2d7-f1bec9902bd3.shtml?refresh_ce-cp

Now who are the owners of Moderna ? The usual suspects - the financial usurers who control the world : first up is fund vanguard, founded by the late christonazi usurer john bogle, but these days controlled by judeonazis fink laurence and kapito robert of blackrock:

https://money.cnn.com/quote/shareholders/shareholders.html?symb=AVD&subView=institutional

Next up is fidelity management, owned by the christonazi puritan dynasty of the johnsons, currently represented by johnson abigail ; third in line is blackrock itself, of judeonazis fink & kapito :

need I continue ? These criminals are the real spreaders !!! Of an utter hoax, that is - more proof will follow shortly.

The second lightning-speed drug maker is Gilead Sciences :

https://www.theguardian.com/world/2020/mar/10/hopes-rise-over-experimental-drugs-effectiveness-against-coronavirus

" Gilead stressed that it was boosting production [of anticovid drug remdesivir] “in anticipation of potential future needs” before knowing whether the trial would show the drug to be safe and effective at treating patients with the virus " :

NOW YOU TELL ME WHAT CAPITALIST CORPORATION WOULD BOOST PRODUCTION BEFORE RECEIVING SCIENTIFIC AND GOVERNMENTAL APPROVAL - RISKING TO LOSE BILLIONS ! THE ANSWER IS, GILEAD KNEW IN ADVANCE THAT REMDESIVIR WOULD BE TRUMPETED AS A SOLUTION TO THE FAKE PANDEMIC (AND THE OWNERS OF GILEAD SCIENCES ARE THE EXACT SAME AS THOSE FOR MODERNA : FINK & KAPITO OF BLACKROCK, THE JOHN BOGLE HEIRS, CAPITAL RESEARCH & MANAGEMENT OF CAPITALFASCIST LOVELACE DYNASTY CURRENTLY HEADED BY ROB LOVELACE, ETC. - BILDERBERG GALORE); "COVID" DOESN´T EVEN EXIST, AND THESE NEW DRUGS AND VACCINES ARE SNAKE OIL TO BE SOLD TO VASSAL GOVERNMENTS FOR A PROFIT, TO BE MADE MANDATORY AND INOCULATED INTO ALL HUMANS WITH DEVASTATING HEALTH AND IMMUNITY DAMAGE.

https://www.thewealthadvisor.com/article/19t-fund-giant-crazy-idea-about-investing

https://en.wikipedia.org/wiki/Jonathan_Bell_Lovelace

THESE DRUGS ARE EXTREMELY HEAVY IN SIDE EFFECTS, TO THE POINT OF LETHALITY FOR THE OLD WEAK AND IMMUNODEFICIENT : IT IS A CRIME AGAINST HUMANITY TO GIVE THEM TO PATIENTS IN THE NAME OF A FAKE VIRUS !!!!

As for Europe, the dominant vax player appears to be astrazeneca, owned by the usual global fund usurers :

https://www.corriere.it/salute/malattie_infettive/cards/guerra-vaccini-chi-vincera/sfida-senza-precedenti_principale.shtml

https://money.cnn.com/quote/shareholders/shareholders.html?symb=AZN&subView=institutional

REFUSE VACCINATION AGAINST A NONEXISTENT DISEASE !!!

A great commentator on youtube wrote on nov.13, 2020 :

PESTIL3NCE

" Not to worry mandatory vaccinations are coming, oh wait sorry. They ' re not going to be mandatory, you simply won´t be able to travel/fly, go to shops, dentist, or hospital without a vaccination certificate. Just the first of many mandatory vaccinations to come, don´t think it will happen? Guess you missed the health secretary talking about mandatory vaccinations & finding a way around the laws protecting the people´s right to choose. "

CHAPTER 5 : HUNTED DOWN SPIED ON TRANSHUMANIZED

https://www.theguardian.com/world/2020/mar/17/israel-to-track-mobile-phones-of-suspected-coronavirus-cases

One of the real main purposes of this giant global hoax it is, to force us all to accept individual tracking via smartphone/apps of everybody´s every single movement and communication, under pretext of emergency legislation (unapproved by Parliaments that have been shut down)

to fight the non-existent pandemic. Plus mandatory facial recognition and sanitary treatments for all but those in power, and the rest of the orwellian panoplia - a capitalfascist´s wet dream of total control come true. And that´s just the beginning - with the same pretext, they are going to push for mandatory subcutaneous microchips for total remote control of all humanity - or even inoculate control chips into people´s bodies with mandatory vaccine shots - FIGHT BACK !!!

https://www.mintpressnews.com/mass-tracking-covi-pass-immunity-passports-slated-roll-15-countries/269006/

https://www.biometricupdate.com/201909/id2020-and-partners-launch-program-to-provide-digital-id-with-vaccines

CHAPTER 6 : NO VIRUS NO DISEASE NO PANDEMIC

https://www.nejm.org/doi/full/10.1056/NEJMoa2001017

Here´s what biochemist David Rasnik had to say in 2020 about the alleged "sars-cov-2" virus :

" The electron microscopy images of the new coronavirus I was talking about were published in the New England Journal of Medicine 2020. I accept that coronaviruses that cause the common cold exist. I am not convinced that a new coronavirus causing Covid-19 has been purified or even really exists. Given the importance of this you’d think the proof of existence would be easy to come by and be confirmed by independent labs around the world.

Zhu (2020) did TEM on cell culture supernatant (Fig. 3A), which looks very much like a coronavirus (see 100 nm reference bar, ideal for identification of the viral family, see attached file).

Fig. 3B shows particles inside a cell. This is the correct thing to do on primary lung tissue. (It’s not clear this was the case, however. See below.) They should have used the same magnification as in 3A in order to identify the particles as virus, in particular, coronavirus. Instead, they used 1µm (1000nm) reference bar.

[ My note : what Doctor Rasnick is saying here is, that these alleged pics of alleged isolated sars-cov-2 viruses look nowhere near the standard size that coronaviruses are supposed to feature :

https://www.clinicalmicrobiologyandinfection.com/article/S1198-743X(20)30363-3/fulltext

"The available viral genome sequences allowed to soon recognize the close relationship between SARS-CoV-2 and SARS-CoV-1, the causative pathogen of the 2002–2004 outbreak, presenting with severe acute respiratory syndrome (SARS).

Both viruses belong to the Coronaviridae family. They are characterized by a single-stranded 30 kb positive-sense RNA and enveloped spherical virions of about 160 nm. The unusual large size of their genome leaves these viruses enough space to rearrange their genes (recombination), thus donating them some genomic plasticity".

Now :

https://jkms.org/DOIx.php?id=10.3346/jkms.2020.35.e84

southkoreans allegedly isolate virus : from the pic scale we can see that the alleged, non-purified viruses are smaller than 100 nm (pic D) - the standard corona size being 160 !!!

Same scam in the zhou paper, the original chinese fakery that triggered the whole pandemy scam :

https://www.nejm.org/doi/full/10.1056/NEJMoa2001017

pic 3A : the 2 purportedly isolate viruses are way smaller than 160 nm !!! And the spikes are nowhere to be seen.]

Back to Doctor Rasnick :

" There are some things not quite clear in the paper. After close re-reading, It looks like the TEM photos, especially Fig. 3B, may not be of primary lung tissue from a patient.

On page 4 the authors say, "Virus isolation from clinical specimens was performed with airway epithelial cells and Vero E6 and Huh-7 cell lines.” This raises the question of a possible artifact, along the lines of Robert Gallo´s viral isolation of HIV. They should have first done TEM directly on primary lung tissue to establish the presence of virus. Culturing virus is fine but its presence must be confirmed by TEM of primary lung tissue.

It is essential to take great pains to accurately identify and characterize any presumed infectious agent present in people with new symptoms. That's where TEM on primary tissue samples from the person with symptoms is essential. This can be followed by culturing the suspect agent in order to purify it and performing TEM again, this time on the cultured virus. As a control, you must also perform TEM on the cultured cells that you have not treated with the suspect virus to make sure a virus had not contaminated the cells. I do not trust experiments using cancer cell lines to culture

virus. Usually, animals that are susceptible are treated with the pure virus to study and confirm its pathology.

Once all the preliminary work is done, which could take up to a year or more, simpler detection methods can be employed so long has their accuracy has been confirmed using gold standards such as TEM.

Look up Koch’s postulates. "

The chinese stated in their report that they had isolated the new virus now called sars-cov-2, termed by them 2019-nCoV, by combining (how?) 2 sequencing methods called Illumina and Nanopore, both of which are highly biased and error-prone :

https://www.nejm.org/doi/full/10.1056/NEJMoa2001017

https://en.wikipedia.org/wiki/Illumina_dye_sequencing

" This piecemeal process allows scientists to see the complete sequence even though an unfragmented sequence was never run; however, because Illumina read lengths are not very long (HiSeq sequencing can produce read lengths around 90 bp long), it can be a struggle to resolve short tandem repeat areas. Also, if the sequence is de novo and so a reference doesn't exist, repeated areas can cause a lot of difficulty in sequence assembly. Additional difficulties include base substitutions (especially at the 3' end of reads) by inaccurate polymerases, chimeric sequences, and PCR-bias, all of which can contribute to generating an incorrect sequence. "

https://en.wikipedia.org/wiki/Chimera_(molecular_biology)

"A chimera can also be an artifact of PCR amplification. It occurs when the extension of an amplicon is aborted, and the aborted product functions as a primer in the next PCR cycle. The aborted product anneals to the wrong template and continues to extend, thereby synthesizing a single sequence sourced from two different templates.

PCR chimeras are an important issue to take into account during metabarcoding, where DNA sequences from environmental samples are used to determine biodiversity. A chimera is a novel sequence that will most probably not match to any known organism. Hence, it might be interpreted as a new species thereby inflating over diversity." :

https://en.wikipedia.org/wiki/Nanopore_sequencing

" Notably, theorists have shown that sequencing via exonuclease enzymes as described here is not feasible.[14] This is mainly due to diffusion related effects imposing a limit on the capture probability of each nucleotide as it is cleaved. This results in a significant probability that a nucleotide is either not captured before it diffuses into the bulk or captured out of order, and therefore is not properly sequenced by the nanopore, leading to insertion and deletion errors. Therefore, major changes are needed to this method before it can be considered a viable strategy.

The use of proteins in biological nanopore sequencing systems, despite the various benefits, also brings with it some negative characteristics. The sensitivity of the proteins in these systems to local environmental stress has a large impact on the longevity of the units, overall. One example is that a motor protein may only unzip samples with sufficient speed at a certain pH range while not operating fast enough outside of the range- this constraint impacts the functionality of the whole sequencing unit. Another example is that a transmembrane porin may only operate reliably for a certain number of runs before it breaks down. Both of these examples would have to be controlled for in the design of any viable biological nanopore system- something that may be difficult to achieve while keeping the costs of such a technology as low and as competitive, to other systems, as possible.[9]

One challenge for the 'exonuclease approach',[32] where a processive enzyme feeds individual bases, in the correct order, into the nanopore, is to integrate the exonuclease and the nanopore detection systems. In particular,[33] the problem is that when an exonuclease hydrolyzes the phosphodiester bonds between nucleotides in DNA, the subsequently released nucleotide is not necessarily guaranteed to directly move into, say, a nearby alpha-hemolysin nanopore. One idea is to attach the exonuclease to the nanopore, perhaps through biotinylation to the beta barrel hemolysin. The central pore of the protein may be lined with charged residues arranged so that the positive and negative charges appear on opposite sides of the pore. However, this mechanism is primarily discriminatory and does not constitute a mechanism to guide nucleotides down some particular path. "

https://en.wikipedia.org/wiki/De_novo_sequence_assemblers

" Reads from second generation technologies (called short read technologies) like Illumina are typically short (with lengths of the order of 50-200 base pairs) and have error rates of around 0.5-2%, with the errors chiefly being substitution errors. However, reads from third generation technologies like PacBio and fourth generation technologies like Oxford Nanopore (called long read technologies) are longer with read lengths typically in the thousands or tens of thousands and have much higher error rates of around 10-20% with errors being chiefly insertions and deletions."

Here´s how the alleged sequencing of sars cov 2 is described in the zhu paper :

" Viral Genome Sequencing

RNA extracted from bronchoalveolar-lavage fluid and culture supernatants was used as a template to clone and sequence the genome. We used a combination of Illumina sequencing and nanopore sequencing to characterize the virus genome. Sequence reads were assembled into contig maps (a set of overlapping DNA segments) with the use of CLC Genomics software, version 4.6.1 (CLC Bio). Specific primers were subsequently designed for PCR, and 5′- or 3′-RACE (rapid amplification of cDNA ends) was used to fill genome gaps from conventional Sanger sequencing. These PCR products were purified from gels and sequenced with a BigDye Terminator v3.1 Cycle Sequencing Kit and a 3130XL Genetic Analyzer, in accordance with the manufacturers’ instructions." :

now : CLC Genomics warns on its own package insert, that it should never be used for diagnostics, only for research purposes !!! :

http://pages.ingenuity.com/rs/202-RSH-885/images/build-manual-plugin-MGM.pdf

p.2.

And : since PCR amplificates only a tiny segment of a genome and never an entire genome, the reconstruction and filling of genome gaps to obtain an entire genome was clearly, totally arbitrary and based on subjective and biased algorithms not on natural/visual observation of a complete viral genome which neither the chinese nor anyone else has been able to properly isolate that is purify so far.

More highlights from the zhu paper :

https://www.nature.com/articles/s41586-020-2012-7

"The association between 2019-nCoV and the disease has not been verified by animal experiments to fulfil the [sic!] Koch’s postulates to establish a causative relationship between a microorganism and a disease."

"No statistical methods were used to predetermine sample size. The experiments were not randomized and the investigators were not blinded to allocation during experiments and outcome assessment."

The german counterparts of these chinese swindlers are no less subservient to bill gates and big pharma, substituting swindle for real science...

continued in entirety here (The bove is 1/4 of the article/book, ws unable to publish all here due to space conbstraint.

https://la.indymedia.org/news/2021/06/300369.php