Finally - US Government Document Release Reveals The Earth Shattering Truth About Covid
It's worse than we thought
I’m stunned. Not only do we now know that yes, there were and still are US biolabs in Ukraine and elsewhere manufacturing and handling very dangerous pathogens, but we now have a detailed explanation of the exact origin of the SARS-CoV-2 virus, which was created at the Wuhan Institute of Virology (and also US biolabs) by Fauci, Dasczak etc. working under an Eco Health Alliance program.
The document revealing this is part of this US Senate release by Senator Rand Paul. When I first saw the screenshot on X, so incendiary was the information contained in it, that I seriously doubted whether it was real. But it is, very real, and this changes everything. Covid was a gain of function virus, engineered in a lab. It probably wasn’t meant to escape, but it did, or somebody intentionally released it. It was spread by aerosols, not droplets, it was only really dangerous to the very old and the immunologically compromised, masks were virtually useless and the mRNA ‘vaccines’ were largely ineffective and potentially very dangerous. Early treatment protocols like hydroxychloroquine and ivermectin were effective - but they were suppressed, dismissed and even banned by governments and the medical profession: let that sink in. All this was known by the illegitimate Biden administration in August 2021, and most likely many months before that.
As a ‘Covid denier’ and ‘anti-vaxxer’ virtually from day one, this confirms all my serious misgivings about the so called ‘Covid pandemic’ since 2020, and my even greater alarm at the rollout of the ‘vaccines’ starting in December 2020. It’s tragic that I and many, many other people who shared those misgivings were cancelled on social media, ostracized by friends, family and work colleagues, lost careers, or even worse, threatened with prosecution and imprisonment. Lawyer Reiner Fuellmich is still rotting in a German prison for his part in setting up the highly effective Corona Investigative Committee, after having been fitted up on embezzlement charges. The naked-faced ‘Covidiots’ and ‘science deniers’ were right, all along. So let’s get straight into it. The opening shot sets the scene for what follows:
1. SARS-CoV-2 is an American-created recombinant bat vaccine, or its
precursor virus. It was created by an EcoHealth Alliance program at the
Wuhan Institute of Virology (WIV), as suggested by the reporting
surrounding the lab leak hypothesis. The details of this program have
been concealed since the pandemic began. These details can be found in
the EcoHealth Alliance proposal response to the DARPAi PREEMPTii program
Broad Agency Announcement (BAA) HR00118S0017, dated March 2018iii – a
document not yet publicly disclosed.
The contents of the proposed program are extremely detailed. Peter Daszak
lays out step-by-step what the organization intends to do by phase and
by location. The primary scientists involved, their roles, and their
institutions are indicated. The funding plan for the WIV work is its own
document. The reasons why nonpharmaceutical interventions like masks and
medical countermeasures like the mRNA vaccines do not work well can be
extrapolated from the details. The reasons why the early treatment
protocols work as curatives are apparent.
These next passages explain exactly what SARS-CoV-2 was and what it was intended to be used as:
SARS-CoV-2’s form as it emerged is likely as a precursor, deliberately
virulent, humanized recombinant SARSr-CoV that was to be reverse
engineered into a live attenuated SARSr-Cov bat vaccine. Its nature can
be determined from analysis of its genome with the context provided by
the EcoHealth Alliance proposal. Joining this analysis with US
intelligence collections on Wuhan will aid this determination.
The purpose of the EcoHealth program, called DEFUSEv in the proposal,
was to inoculate bats in the Yunnan, China caves where confirmed SARSCoVs
were found. Ostensibly, doing this would prevent another SARS-CoV
pandemic; the bats’ immune systems would be reinforced to prevent a
deadly SARS-CoV from emerging. The specific language used is “inoculate
bats with novel chimeric polyvalent spike proteins to enhance their
adaptive immune memory against specific high-risk viruses.” Being
defense-related, it makes sense that EcoHealth submitted the proposal
first to the Department of Defense, before it settled with NIH/NIAID.
The BAA response is dated March 2018 and was submitted by Peter Daszak,
president of EcoHealth Alliance.
SARS-CoV-2 was developed originally as a live vaccine, an aerosolised virus which was intended to mass immunise bats in caves in order to prevent any further deadly SARS-CoV viruses being transmitted from bats to humans. For this purpose, it was deliberately ‘humanized’, i.e. made easily transmissible in humans. It is likely that the original Wuhan SARS-CoV-2 strain which ‘escaped’ from the lab was only the precursor virus for this vaccine and had not yet been fully modified in order for it to be used as the live bat vaccine. So it was a work in progress which somehow ‘escaped’ from the lab in Wuhan (and possibly from other labs which had also developed this live vaccine precursor virus).
But the entire research project should not have been happening anyway because it was rejected by DARPA precisely because it sailed too close to being “gain of function” which was banned. That didn’t stop Fauci or Daszak from ploughing ahead anyway and given what we now know of Obama’s involvement in setting up biolabs in Ukraine and elsewhere, it’s likely that the covert project went ahead with Obama’s full knowledge and blessing.
DARPA rejected the proposal because the work was too close to violating
the gain-of-function (GoF) moratorium, despite what Peter Daszak says
in the proposal (that the work would not). As is known, Dr. Fauci with
NIAID did not reject the proposal. The work took place at the WIV and
at several sites in the US, identified in detail in the proposal.
The document then expands upon the nature of SARS-CoV-2 and its original purpose as a live bat vaccine:
2. SARS-CoV-2, hereafter referred to as SARSr-CoV-WIV, is a synthetic
spike protein chimera engineered to attach to human ACE2 receptors and
inserted into a recombinant bat SARSr-CoV backbone. It is likely a live
vaccine not yet engineered to a more attenuated state that the program
sought to create with its final version. It leaked and spread rapidly
because it was aerosolized so it could efficiently infect bats in caves,
but it was not ready to infect bats yet, which is why it does not appear
to infect bats. The reason the disease is so confusing is because it is
less a virus than it is engineered spike proteins hitch-hiking a ride
on a SARSr-CoV quasispecies swarm. The closer it is to the final live
attenuated vaccine form, the more likely that it has been deattentuating
since initial escape in August 2019.
There you go. The bat coronavirus wasn’t the main story, the engineered spike proteins were. The SARS-CoV-2 whole live virus was merely the vehicle which was used in order to (as originally intended) infect millions of bats in caves in Yunan Province with the engineered spike proteins, thus invoking a strong immune response which would prevent the bats supposedly from transmitting dangerous SARS-CoV variants to the human population. As it turned out, the incomplete precursor virus, SARSr-CoV-WIV, escaped from the lab and the spike proteins which were hitching a ride on its back rapidly infected the entire global human population, with devastating consequences for many.
It was the toxic spike proteins which did all the damage, but they could only do so if the virus they were riding piggy-back on was able to multiply rapidly in the air passages of its human hosts. And for the vast majority of humans, especially younger, healthy humans, it was not able to do that. The virus was prevented from replicating in the upper airways, even before it was able to get deeper into the lungs and into the bloodstream. Humans, as it turns out, have strong natural immunity to beta-coronaviruses, on account of having been previously exposed to e.g. common cold variants for centuries! Who knew? Not the mRNA/DNA ‘vaccine’ developers apparently and their ‘following the science’ cheerleaders across governments. They came up with a cunning plan to mass immunize the whole of humanity by causing each human body to manufacture trillions of the toxic spike proteins, not in the upper air passages where they might have provoked a useful immune response, but in the body itself! In particular in the bloodstream and the internal organs where (surprise, surprise) the bio-engineered toxic spike proteins did immense damage. That decision, and the scandalous coercive/mandatory mass ‘vaccination’ program initiated by governments worldwide, plus the deliberate denial of effective early treatment protocols and the intentional, highly organised scaremongering and propaganda campaign enabled by lockdowns, will probably go down in history as the greatest ever crime committed against humanity.
The vast majority of humanity was not at risk from Covid. There was no need for lockdowns and no need for ‘vaccines’:
SARSr-CoV-WIV is not meant to kill the bats, but to immunize them. This
nature may explain its general harmlessness to most people, and its
harmfulness to the old and comorbid, who are in general more susceptible
to vaccine reactions. The asymptomatic nature is also explained by the
bat vaccine-intention of its creators (a good vaccine does not generate
symptoms). Such effects would be expected of an immature vaccine, or a
vaccine being reverse engineered from a more virulent form into an
attenuated form. The spike protein effect on ACE2 receptors exacerbates
the harmfulness in accordance with age and comorbidity. The nature of
SARSr-CoV-WIV’s deattentuation will also indicate future virulence,
though knowing its nature at last neutralizes the threat as effective
treatments can be applied with confidence.
Known effective early treatment protocols were deliberately suppressed. In the UK, they even killed elderly, very sick people intentionally with massive overdoses of hydroxychloroquine to ‘prove’ that the drug didn’t work (the Oxford Recovery trials). The people who funded and ran those trials should be in prison. Trump was ridiculed for wanting to ‘inject people with bleach’ and the FDA notoriously ridiculed the idea of using a ‘horse dewormer’ (Ivermectin) to treat Covid.
Because of its (now) known nature, the SARSr-CoV-WIV’s illness is readily
resolved with early treatment that inhibits the viral replication that
spreads the spike proteins around the body (which induce a harmful
overactive immune response as the body tries to clear the spikes from
the ACE2 receptors). Many of the early treatment protocols ignored by
the authorities work because they inhibit viral replication or modulate
the immune response to the spike proteins, which makes sense within the
context of what EcoHealth was creating. Some of these treatment protocols
also inhibit the action of the engineered spike protein. For instance,
Ivermectin (identified as curative in April 2020) works throughout all
phases of illness because it both inhibits viral replication and
modulates the immune response. Of note, chloroquine phosphate
(Hydroxychloriquine, identified April 2020 as curative) is identified
in the proposal as a SARSr-CoV inhibitor, as is interferon (identified
May 2020 as curative).
Fauci and Daszak knew, even before their Frankenvirus escaped, that HCQ was effective as an inhibitor. They should be in prison too.
Then there’s the ‘vaccines’ and this is where the shit really hits the fan and probably explains why the ‘Covid pandemic’ went from a rapidly self-limiting and not very dangerous ‘bad cold’ to a global disaster:
The gene-encoded, or “mRNA,” vaccines work poorly because they are
synthetic replications of the already-synthetic SARSr-CoV-WIV spike
proteins and possess no other epitopes. The mRNA instructs the cells to
produce synthetic copies of the SARSr-CoV-WIV synthetic spike protein
directly into the bloodstream, wherein they spread and produce the same
ACE2 immune storm that the recombinant vaccine does. Many doctors in the
country have identified that the symptoms of vaccine reactions mirror
the symptoms of the disease, which corroborates with the similar
synthetic nature and function of the respective spike proteins.
The vaccine recipient has no defense against the bloodstream entry, but
their nose protects them from the recombinant spike protein quasispecies
during “natural infection” (better termed as aerosolized inoculation).
Furthermore, the EcoHealth proposal states that a “vaccine approach lacks
sufficient epitope coverage to protect against quasispecies of
coronavirus.” Consequently, they were trying to make vaccines work by
“targeted immune boosting via vaccine inoculators using chimeric
polyvalent recombinant spike proteins.” The nature of using a spike
protein vaccine with one epitope against a spike protein vaccine with a
quasispecies may explain the unusual (and potentially detrimental)
antibody response amongst the vaccinated to the new COVID variants.
Fundamentally, the knowledge the proposal provides signals that the risk
of Antibody Dependent Enhancement (ADE) from vaccination should be
evaluated with high priority, on top of the reality that single-epitope
vaccines will have little effect against SARSr-CoV-WIV, as indicated in
the proposal.
The potential for SARSr-CoV-WIV to deattentuate requires immediate
attention. Live vaccines have been found to deattentuate in the past.
If this is the case with SARSr-CoV-WIV, then the mass vaccination
campaign actually performs an accelerated gain-of-function for it. Since
it is designed for bats off of a human-susceptible SARS-CoV, vaccinating
humans against it actually gains its function back towards a more
deattenuated human-susceptible form.
Improving the SARSr-CoV-WIV spike protein to gain robustness against monoclonal
vaccines is one of the steps of the DEFUSE program. The mechanism to improve the
SARSr-CoV-WIV spike protein (other than direct engineering) is to challenge it against
animals that have spike protein-only antibodies. The attenuated virus
will either die or adapt its form to neutralize the spike protein-only
antibodies. The intent was to perform this task against humanized mice
and then “batified” mice. Instead, it was done with the world’s
population.
There was no need for a systemic ‘vaccine’ (injected into the muscle which, contrary to the lies of pharmaceutical companies, did make its way into the circulating blood stream and hence to every organ in the body) because natural mucosal (nasal) immunity was sufficient in almost all cases to prevent the virus from replicating in the nasal passages, thus neutralizing the toxic spike proteins before they could do damage in the body. In fact, mass vaccinating into the ‘pandemic’ did far more harm than good, making many more people even more susceptible to emerging Covid variants. The early warnings were there. I wrote about them in January and February 2021 when folks started dropping dead in care homes soon after being vaccinated.
https://climatecontrarian.wordpress.com/2021/01/29/one-third-of-vaccinated-residents-at-a-basingstoke-nursing-home-are-now-dead-bbc-calls-it-a-covid-outbreak/
https://climatecontrarian.wordpress.com/2021/02/25/what-is-behind-the-sharp-rise-in-covid-deaths-soon-after-vaccination/
But to question the efficacy, even the safety, of the miraculous, wondrous, innovative new Covid ‘vaccine’ at the time was considered to be heretical and anti-science. You were a tinfoil hat wearing conspiracy theorist antivaxxer for daring to question ‘the science of immunology’ - just as you were (and still are) for daring to question the Settled Science of Climate Change.
I also wrote about Geert Vanden Bossche’s early warnings re. mass vaccinating during a pandemic and the real possibility of ADE (antibody dependent enhancement):
In pursuing a policy of mass vaccination, the government is in fact conducting a very dangerous and medically unnecessary experiment upon humanity, one which the actual science does not justify. Why?
The leaky vaccines are here – the Covid vaccines. They are being rolled out to millions without a second thought about the consequences; in fact they are being outrageously coerced by governments worldwide. Do they actually want to see us all die if something goes wrong? The most vulnerable may initially be the unvaccinated, but even those vaccinated may be vulnerable to any virulent new variants which emerge as a direct consequence of this insane mass medical intervention. In that regard, remind me again why Blair was so keen to have partially vaccinated people wandering around for weeks longer than recommended by the manufacturers themselves, after receiving only one jab? Remind me again of the fact that many millions in Third World countries will indeed not be vaccinated for quite some time.
https://climatecontrarian.wordpress.com/2021/03/08/killing-the-flock-the-insanity-of-mass-vaccinating-with-non-sterilising-vaccines/
Again, in April 2021, I was pointing out the worrying evidence that vaccinated people were becoming more susceptible to emerging variants:
https://climatecontrarian.wordpress.com/2021/04/12/vaccinated-people-are-eight-times-more-likely-to-be-infected-with-the-south-african-variant/
And how vaccinated NHS workers were getting sick afterwards:
https://climatecontrarian.wordpress.com/2021/04/04/bmj-unprececedented-levels-of-sickness-after-vaccination/
Then in September, I picked up the theme again:
https://climatecontrarian.wordpress.com/2021/09/25/covid-vaccines-the-unpalatable-truth-plus-why-scientists-and-politicians-may-have-committed-original-antigenic-sin/
In December 2021, I highlighted the brilliant Sucharit Bhakdi pointing out exactly why natural mucosal immunity was so effective and why the ‘vaccines’ weren’t - something which we now know the US government was well aware of at least as early as August 2021.
https://climatecontrarian.wordpress.com/2021/12/01/boosters-who-needs-them-plus-why-the-mrna-dna-vaccines-do-not-protect-against-infection/
But still they queued to get jabbed, couldn’t wait for it, were gagging for it even. When Boris ‘Pol Pot Belly’ Johnson gracefully let us all out of prison in the summer of 2021 I was touring Scotland and I gasped in horror at the queues of people lining up to get their miraculous ‘Covid cure’ outside a pop up NHS vaccination centre in some small town whose name eludes me now. I despair, I really do. And don’t even get me started on the hideous masks!
It’s all come out in the wash now. Will anyone go to prison for what was done to us? I doubt it. If not, we can’t really call ourselves a civilised society anymore.



Nice summary.
As you know, these moronic , (the followers),and criminal (the instigators), behavior permeates all governments, and most other organizations. I don't know how we continue without real accountability. Things may have to get uncomfortable.
We live in a technocracy run by middle manager types who are interested only in stabbing each other in the back to obtain promotion. They rely on those boffin chappies to tell them what's cool in (bio)science and they haven't a clue whether what they're told is right, wrong or just misleading.
None of them either as an individual or as a group is capable of handling the problems that a technological society throws up. This is our doom (OK I've been watching Lord of the Rings again).
Until we can find a political system under which good policy is made in response to novel and complex problems, we are fated to spiral down to complete collapse. Have a nice day.