There is a long article here about why Trump didn’t fire Fauci. It is rather boring, but it reminds us of one interesting fact.

The National Institute of Allergy and Infectious Diseases (NIAID), which coordinated and largely funded the development of the covid virus, was born in blood.

The then Vice President Dick Cheney wanted to consolidate and expand the US biodefense effort.

On September 18, 2001, a number of national media outlets were sent letters containing anthrax.

The resulting alarm wasn’t enough so three weeks later a second round of letters was sent. Twenty-two people were infected with anthrax, five of whom died.

The anthrax in those letters was genetically typed to a strain isolated and developed by the Ames Laboratory operated by the Department of Energy in Iowa.

So this terrorist attack was an inside job to gin up support for a big expansion in bioweapons research.

A Dr Fauci, till then only known for botching the response to HIV, was installed to run the NIAID without oversight.

Fauci was a morally flexible ecoloon who believed that mankind would get a comeuppance from being out of balance with Nature.

With Nature not providing enough plagues for his satisfaction, Fauci sped up the process by funding gain of function research into making designer viruses.

Gain of function research was outlawed in the US in 2012. In 2016 Fauci got around that ban by funding gain of function research at the Wuhan Institute of Virology.

In doing so he coordinated with other ecoloons including Bill Gates and Peter Daszak of EcoHealth Alliance.

Gates had been yabbering for decades about humanity being a plague on the planet and he wanted a vaccine to make people sterile.

It would be hard to imagine people volunteering to submit to such a vaccine but this didn’t stop Gates from dreaming, and plotting.

Daszak was more upfront about just wanting to kill people. A decade ago he used to decorate EcoHealth conferences and dinners with images of skulls:

As popular culture, informs us, people who use skulls as decorations are the baddies.

The brains behind the technology used to put the virus together was provided by Dr Ralph Baric of the University of North Carolina.

Covid was essentially a US Government creation with the Wuhan Institute of Virology acting as a contractor.

Bioweapons researchers think that HIV is a wonderful disease because it doesn’t kill the infected straight away but gradually weakens their immune systems so that they die of other viruses, bacteria, fungi and cancers as the years pass.

The infected aren’t alarmed enough initially to stop the spread of the disease.

Take Freddie Mercury as an example. He is thought to have been infected with HIV in the late 1970s.

He was diagnosed with HIV in 1986 and died in 1991 from bronchial pneumonia resulting from HIV. In the early 1980s when he was still giving concerts, Freddie Mercury would have thought that he had had a mild case of HIV.

HIV’s big drawback as a bioweapon was that it was hard to spread – only by fluid contact.

Then SARS came along in 2003. This was a highly infectious respiratory disease that even spread vertically between floors of apartment buildings via the plumbing.

The shortcoming of SARS as a bioweapon was its 30% case fatality rate which got people upset enough to use contact tracing to stop transmission.

The solution lit upon by Fauci and friends was to lower the case fatality rate of SARS so that people wouldn’t be alarmed enough to stop transmission, and insert bits of HIV to do some long term killing.

The former was predicted by the Johns Hopkins Center for Health in a 2017 exercise which on page six predicted that the next viral plague will be based on the SARS virus and have a case fatality rate of 0.6% – spookily accurate.

As with Bill Gates’ Event 201, the 2017 exercise was more about narrative management and overcoming vaccine hesitancy than actually combatting the disease.

Bill Gates’ activities during this time included loading up on stocks that would benefit from providing the cure to the virus.

The Gates Foundation first bought a position in BioNTech in September 2019, two months before the pandemic hit.

It invested $55 million in the biotech, with the potential for total funding to reach $100 million. BioNTech’s subsequent price performance is shown in this graph:

Killing people to save the planet is one thing but to make money from it at the same time you need to have a vaccine to sell.

The US Government started developing a covid vaccine in partnership with Moderna in 2015.

This would then justify Fauci and Francis Collins at the National Institutes of Health getting royalty payments from Moderna.

The tight relationship with Moderna is also shown by the fact that a sequence from a Moderna patent from 2017 is incorporated in the covid genome.

Apparently this was to make the thing more infectious. It already had more than enough short term fatality and the HIV inserts were the real payload of the virus.

But is the covid vaccine also a bioweapon? It turns out that it is. This is a succinct case for malicious intent in the design of the covid vaccines put forward by Tom Czerniawski:

The evidence of this malice lies in the vaccine spike protein, replication of which is instructed via messenger RNA. C-19’s infectiousness is owed to its spike protein, and that’s due to a gene feature of the protein called a furin cleavage site.

Now here’s the vaccine spike protein. Slightly modified – the creators included a handful of point mutations claimed to lock the protein in a safe pre-fusion configuration, rendering it unable to interface with cells as it would be in its post-fusion S1-S2 sub-unit configuration:

Only one problem. The vaccine spike’s creators preserved that furin cleavage site.

Furin and cathepsin are proteases, which are enzymes endogenous to the human body that cleave proteins in specific ways. When C-19’s spike hits those proteases, it unlocks into its highly pathogenic post-fusion S1-S2 sub-unit configuration, one of its main routes of infection.

The vaccine spike was claimed not to do that. That’s not how things turned out. It can unlock, in one of two ways, forming slightly different S1-S2 sub-units, or it can “explode like a peptide grenade.” Turns out there was no way to ensure the stability of those point mutations.

How do we know this was a malicious act? The C-19 mRNA vaccines share a common research ancestor: a failed attempt at an HIV vaccine. In that instance, the creators specifically excluded the HIV spike protein’s furin cleavage site, demonstrating foreknowledge that its inclusion meant preserving a large part of the parent virus’ pathogenic profile. They then went on to preserve the furin cleavage site in the C-19 vaccines with this knowledge.

Fauci and friends would have known of the effect of preserving a cleavable furin cleavage site.

The fact that the vaccinated have a higher rate of covid infection than the unvaccinated is now well known.

According to this article from the Washington Post, those who were vaccinated but never had covid were four times as likely to have severe illness resulting in hospitalization or death compared to the unvaccinated.

How this happens is explained by an oncologist who is seeing a lot of his patients suddenly coming out of remission:

Scientifically, I was reading reports that the booster was leading to a big excess of antibodies at the expense of the T-cell response and that this T-cell suppression could last for three weeks, if not more. To me, this could be causal as the immune system is being asked to make an excessive response through the humoral inflammatory part of the immune response against a virus variant which is no longer in existence in the community. This exertion leads to immune exhaustion, which is why these patients are reporting up to a 50% greater increase in Omicron, or other variations, than the non-vaccinated.

There is another sign that the vaccines were designed to do more harm than good.

This paper found that “the numbers and frequencies of hematopoietic stem progenitor cells in the umbilical cord blood decreased significantly in donors with previous SARS-CoV-2 infection and more so with COVID-19 vaccination via the induction of apoptosis, likely mediated by IFN-g-dependent pathways.”

Hematopoietic stem progenitor cells can be separated out and used to treat those with hematological disorders.

The authors of the paper were more worried about the loss of that business than the effect on the baby at the end of the umbilical cord. No wonder that birth rates in highly vaccinated countries have cratered.

And those crazy stories about how the vaccine genetic material gets into our DNA? This paper reports that:

On the other hand, we report that after pre-exposure to mRNA-LNPs, the resistance of mice to heterologous infections with influenza virus increased while Candida albicans decreased. The diminished resistance to Candida albicans correlated with a general decrease in blood neutrophil percentages. Interestingly, mice pre-exposed to the mRNA-LNP platform can pass down the acquired immune traits to their offspring, providing better protection against influenza.

So if you get injected with the jiggery-pokery of one of the mRNA vaccines, your descendents will have higher resistance to influenza but be more prone to yeast infections like Candida, even unto the seventh generation?

Australia is currently suffering a very high excess mortality rate of 17%. This correlates with vaccination rate:

Friends and relatives suddenly dropping dead, vaccinated but irrespective of covid infection status – this is the bitter harvest of the covid vaccines which were pushed to the limit of the legal process and beyond.

Younger males have a high death rate from myocarditis because they express higher levels of the ACE-2 receptor.

But most of the excess deaths are concentrated in the wrinklies. This article says the excess death rate in the 85+ cohort is 8%. That is one in twelve in this age group being killed each year by the effects of vaccination.

At the same time the US health establishment was creating covid and its vaccine, there were also researching existing drugs that might have an effect against a corona virus.

Thus there is the existence of this patent that was filed by the US Department of Health in 2015. It shows the efficacy of hydroxychloroquine against MERS and SARS:

The units are micromoles/litre.  With a molecular weight of 335.9 grams/mole, the IC50 translates as 2.7 µg/ml. Which would be therapeutically useful.

The health authorities knew this when the covid virus escaped the lab in late 2019, but remained silent.

They didn’t want anything to compete with their vaccines which their royalty payments depended upon.

And there was a lot of international coordination in achieving this.

The French health authorities put hydroxychloroquine on the list of poisonous substances on October 8, 2019, just before the outbreak.

Queensland banned hydroxychloroquine on 7th April, 2020 and lifted that ban on 12th March, 2022 without explanation or an apology for the people killed by their edict. Our country is run by really stupid people – but you already knew that.

Ivermectin must be better than hydroxychloroquine because it is still banned.

To counter covid we have to counter what it was designed to do. It was designed as a highly infectious form of HIV. To that end it has four inserts from HIV, no more, no less. This diagram shows what each insert does:

So, if you get a hyperinflammatory response to covid and die with a ventilator strapped to your face, you can thank the QTNSPRRA sequence.

The Gp120 sequence gets covid across the blood/brain barrier and into the immunoprotected central nervous system.

From where the virus can do some long term degradation of the immune system via persistent inflammation.

The long term degradation of the immune system can be quantified by testing for the right blood markers.

This paper found that patients with long covid had highly activated innate immune cells, lacked naive T and B cells and showed elevated expression of type I IFN (IFN-β) and type III IFN (IFN-λ1).

The strongest indicators of long covid are the inflammatory mediators IFN-β, PTX3, IFN-γ, IFN-λ2/3 and IL-6.

For covid to be developed in the US health establishment, important policy safeguards had to be disabled and people with morals removed from their positions.

This was Fauci’s work. And people had to be bought off. This was more Bill Gates’ job.

He distributed US$300 million among media companies so they wouldn’t criticise the vaccines.

This is why Fox News was silent on the vaccines; money was more important than news or the truth.

Early in the pandemic a bloke was bought off with $40 million in research funding in return for a report that said that ivermectin doesn’t work.

Nobody was neglected in shutting up people who could prove to be problematic. Thus this graphic of funding is provided by the pension plan of the American Board of Pediatrics:

Their funding went through the roof in 2020. They also had a big leg up from their investment performance.

No doubt they were told to go long Pfizer and Moderna. Killing adults for fun and profit, as per Fauci and Daszak, is one thing.

Killing children is incompatible with a civilised society. Especially by the people self-selected to look after their health interests.

The moneychangers are in the temple. Moloch is amongst us.

One puzzle at the time of the lab leak was “Why would the Chicoms release a deadly virus if they didn’t have the vaccine ready to go?”

They didn’t have a vaccine because that was being developed in the US, including being tested in Baric’s lab.

The fact that the Chicoms have gone “let it rip” suggests that they are not on top of the science after all.

Their current high fatality rate is likely due to low vitamin D levels.

This paper found that the elderly in China have an average vitamin D level of 17.3 ng/ml whereas Americans in that age group have an average of 31.7 ng/ml.

While this 2019 paper on Israeli covid patients found that patients with vitamin D deficiency (less than 20 ng/ml) were 14 times more likely to have severe or critical disease than those with a level of 40 ng/ml or higher.

Locking people up in apartment blocks for months on end would have reduced levels further from the 2019 data.

ACE-2 isn’t the only receptor that covid uses to get into our cells. It also used the CD147 and GRP78 receptors as well as mediators.

Once the body’s immune response is activated the intercellular space becomes dangerous for covid virions.

So they then cause the cells they have infected to fuse with neighbouring cells, creating synctia.

Where they want to end up is in immunopriveliged tissue such as the brain and the gut-associated lymphatic tissue. To that end they form tunnelling nanotubes.

You don’t want your covid infection to get to the stage of the tunnelling nanotubes. To thwart that it is necessary to keep your immune system as strong as possible.

To that end you will need to keep your vitamin D level as high as possible. The highest level ever achieved naturally is 86 ng/ml by a farmer in Puerto Rico.

The theoretical upper limit before side effects might kick in is 150 ng/ml. Also dose yourself with things that will bind to the covid virions.

Ivermectin is the most proficient of these but a number of other things such as ursolic acid might prove to be useful.

And covid turns off the vitamin D receptor on cells so those receptors need to be reactivated with things like quercetin and resveratrol.

There is increasing evidence that a drug cocktail made for HIV, Truvada, works on covid too.

Truvada is off patent but nevertheless costs US$24,000 per annum. And for Truvada to work it has to be started before the kidneys have taken too much damage.

Thus the importance of testing for Estimated Glomerular Filtration Rate which tells us how much toxic load the kidneys can handle.

Of course Australian governments are paying hundreds of millions of dollars to start vaccine manufacturing, being always a reliable contra-indicator of what to do.

There will never be a vaccine for covid. We are better off setting up drug manufacturing for ivermectin, vitamin D, the molecules in Truvada and all the other things that might work and tweak efficacy.

Just as developing drugs for gliablastoma is difficult due to the blood/brain barrier, defeating covid in brain tissue is going to be difficult but the sooner we start, the better.

Covid has progressed like a slow motion train wreck. We knew it had HIV inserts from 31st January, 2020 when the paper saying that was posted online.

So, it was designed to be airborne HIV. And to defeat it we have to treat it like airborne HIV. Life has imitated art.

The next big thing will be testing for CD4 and CD8 levels and the other indicators of degrading immune systems.

Then panic and anger as people realise what has been done to them by people who have consistently lied to them.

One interesting thing to watch will be the loyalty of the regime’s foot soldiers, the FBI and CIA agents who have enforced silencing of covid criticism.

When they see their own families dying and their colleagues dying, will they get angry enough to do something about it?

David Archibald is the author of The Anticancer Garden in Australia.