The GOAL of the perpetrators of the COVID fraud is TOTAL GLOBAL CONTROL, as confirmed in the Snowden revelations.

Journalist Glenn Greenwald says we are absolutely very close to the point where we have a system in place where you cannot cross certain lines with opinions you express...or dissidence that you want to organise....without being called extremist,
and being criminalised.

This turnkey TYRANNY that Snowden warned us about is coming closer, and closer ....

10minute Montage on Odysee:
https://odysee.com/@FreedomTirade:f/ABSOLUTELY-CLOSE:1?r=


"The House of Medicine is on Fire right now "
-Dr.Peter MC Cullough MD

"A 'virus' so weak it could have been cured with a bit of well co-ordinated fresh air"
- Brett Weinstein PhD Biology

The biggest ever misadventure in biological research and operations, worldwide, is unfolding before our eyes, in real time.

They will not give up until
das Untergang...
So... guess who's back!

Pursue HEALTH
Resist TYRANNY
@freedomtirade

Trapped Burning Man Attendees Report “Ebola-Like” Illness as the Situation Turns from Bad to Worse

“... there's some sort of virus on the loose at Burning Man that causes boils/vomiting/hemorrhaging. Apparently, that's why they're not letting people in.”

https://vigilantnews.com/post/trapped-burning-man-attendees-report-ebola-like-illness-as-the-situation-turns-from-bad-to-worse

Follow @Vigilant_News

"Methods: We generated an infectious EBOV [EBOLA] clone that lacks the MLD and assessed its virulence in ferrets compared with wild type virus."

Published 28th June 2023

https://pubmed.ncbi.nlm.nih.gov/37379580/

https://twitter.com/robinmonotti/status/1698458645254615271

In cinemas September 7
🎉 ☮️ ❤️

The WHO’s Proposed Treaty Will Increase Man-Made Pandemics. - Meryl Nass MD

"In 1973 genetic engineering (recombinant DNA) was discovered by Americans Herbert Boyer and Stanley Cohen, which changed the biological warfare calculus. Now the US had regained a technological advantage for this type of endeavor.

Under the guise of preparing their defenses against biowarfare and pandemics, nations have conducted “dual-use” (both offensive and defensive) research and development, which has led to the creation of more deadly and more transmissible microorganisms. And employing new verbiage to shield this effort from scrutiny, biological warfare research was renamed as “gain-of-function” research.

How Would You Create a Biological Warfare Agent?
Gain-of-function research is a euphemism for biological warfare research aka germ warfare research. It is so risky that funding it was banned by the US government (but only for SARS coronaviruses and avian flu viruses) in 2014 after a public outcry from hundreds of scientists. Then in 2017 Drs. Tony Fauci and Francis Collins lifted the moratorium, with no real safeguards in place. Fauci and Collins even had the temerity to publish their opinion that the risk from this gain-of-function research was ‘worth it.’ 

What does gain-of-function actually mean? It means that scientists are able to use a variety of techniques to turn ordinary or pathogenic viruses and bacteria into biological weapons. The research is justified by the claim that scientists can get out ahead of nature and predict what might be a future pandemic threat, or what another nation might use as a bioweapon. The functions gained by the viruses or other microorganisms to turn them into biological warfare agents consist of two general but overlapping categories: enhanced transmission and enhanced pathogenicity (illness severity).

1) Enhanced transmissibility may result from:
a)  needing fewer viral or bacterial copies to cause infection,
b)  causing the generation of higher viral or bacterial titers,
c)  a new mode of spread, such as adding airborne transmission to a virus that previously only spread through bodily fluids,
d)  expanding the range of susceptible organs (aka expanded tissue tropism); for example, not only respiratory secretions but also urine or stool might transmit the virus, which was found in SARS-CoV-2, 
e)  expanding the host range; for example, the virus is passaged through humanized mice and thus acclimated to the human ACE-2 receptor, infecting humans preferably to bats or other animals, which was found in SARS-CoV-2, 
f)  improving the ability to enter cells; for example, by adding a furin cleavage site, which was found in SARS-CoV-2
2) Enhanced pathogenicity:
a)  Instead of causing a milder (or no) illness, the pathogen would be reengineered to cause severe illness, incapacity or death, using a variety of different strategies, including the production of toxins or ability to evade immunity.  
b)  SARS-CoV-2 had unusual homologies (identical short segments of nucleotides) to human tissues and the HIV virus, which may have caused or contributed to the late autoimmune stage of illness, an impaired immune response and ‘long COVID.’ 

Illogical Responses to Odd Pandemics
The genomes of both SARS-CoV-2 (start at minute 5) and the 2022 monkeypox (MPOX) virus led to early suspicions that both were pathogens originating in laboratories. The group of virologists assembled by Drs. Fauci and Farrar for a secret phone call on February 1, 2020 identified 6 unusual (probably lab-derived) parts of the SARS-CoV-2 genome--and more have been suggested subsequently. 

according to the CDC it occurs in one in 175 first-time vaccine recipients.  
I have not seen a study with rates of myocarditis for Jynneos, but there was an unspecified elevation of cardiac enzymes in 10 percent and 18 percent of Jynneos recipients in two unpublished prelicensure studies available on the FDA website.

My guess for the mRNA COVID vaccines is that they cause myocarditis, if defined as a rise in troponin levels following vaccination, in the same general range (between 1 in 5 and 1 in 250 recipients per dose).  However, the vast majority of cases are probably asymptomatic and will not be diagnosed unless you screen for them.
Why would our governments push 5 separate vaccines all known to cause myocarditis on young people who are at extremely low risk from COVID?  Monkeypox simply causes a few eruptions (like shingles) for 1-4 weeks unless the infected person is severely immunocompromised.

The Genomic Sequencing Conundrum
And governments are to commit to building biolabs that must include genomic sequencing. No explanation has been forthcoming about why each nation needs to install its own genome sequencing laboratories. Of course, they would sequence the many viruses that will be detected as a result of the pathogen surveillance activities nations must perform, according to the WHO treaty draft. But the same techniques can be used to sequence human genomes.

Genomes offer great potential profits, as they may reveal the secrets of immunity to certain diseases. However, they may also reveal genetic weaknesses at which weapons could be aimed."

Read more:
https://anthraxvaccine.blogspot.com/2023/09/the-whos-proposed-treaty-will-increase.html?m=1

RECOMBINANT DNA TECHNOLOGY or "rDNA":

"Recombinant-DNA (rDNA) technology—the way in which genetic material from one organism is artificially introduced into the genome of another organism and then replicated and expressed by that other organism—was invented largely through the work of Herbert W. Boyer, Stanley N. Cohen, and Paul Berg, although many other scientists made important contributions to the new technology as well.

Boyer’s Work with rDNA and Bacteria

After Paul Berg’s 1971 landmark gene-splicing experiment, the next landmark in the development of modern biotechnology was the insertion of rDNA into bacteria in such a way that the foreign DNA would replicate naturally (see Figure). This step was taken in 1972 by Boyer (b. 1936) at the University of California, San Francisco (UCSF), in collaboration with Cohen (b. 1935) of Stanford University.

November 1972 found both Boyer and Cohen in Hawaii giving papers at a U.S.-Japan joint meeting on plasmids. A plasmid is DNA, found especially in bacteria, that is physically separate from and can replicate independently of the bacterium’s chromosomal DNA. While Boyer was describing his data showing the nature of the DNA ends generated by EcoRI cleavage, Cohen was reporting on a procedure recently discovered in his laboratory that enabled bacteria to take up plasmid DNA and produce offspring that contained self-replicating plasmids identical to the original implant—clones. Over sandwiches late one night at the conference, the two men laid plans for a collaborative project to discover what genes are present on plasmids and how they are arranged.

Boyer and Cohen soon moved on to more complicated cloning experiments. They joined tetracycline-resistant plasmids with kanamycin-resistant plasmids—kanamycin being another antibiotic—and inserted them in E. coli. Next they showed that genetic materials could indeed be transferred between species, thereby disproving a long-held myth. They snipped a piece of Staphylococcus plasmid (Staphylococcus is the bacteria responsible for staph infections), spliced it with one of the many E. coli plasmids, and inserted the whole in E. coli. The DNA from Staphylococcus, a different species of bacteria, was successfully propagated in E. coli. An even greater triumph of interspecies cloning was the insertion into E. coli of genes taken from the South African clawed frog.

Boyer and Cohen, as well as other scientists involved in cloning experimentation, soon recognized the feasibility of using bacteria into which human genetic information was incorporated to duplicate the body’s natural means of fighting disease and to remedy birth disorders."

https://t.me/robinmg/29995

https://sciencehistory.org/education/scientific-biographies/herbert-w-boyer-and-stanley-n-cohen/

My apologies for a long post instead of a link. This text was sent to me as an email.
If it won’t fit, I’ll endeavour to find a link.
I think this is very important.
I’m often challenged with “Polio was all but eliminated by vaccines. Surely you can’t argue with that track record?”
This post provides all the substrate you could want in order to expose the persistent lies & corruption.
That’s a track record only an evil
person would celebrate.
As an undergraduate, I knew that what we call polio was, in clinical appearance, the same as flaccid paralysis and recall being taught in mechanistic toxicology that poisoning with various metal vapours, inhaled in certain occupational industrial settings, often sadly resulted in exactly this severe neurological disorder. I don’t think it occurred to any of us in the early 1980s just how much these seemingly different illnesses overlapped, indeed, were & are the same. Polio joins HIV and in my view, SARS-CoV-2, in the category marked “Fraudulent disease attribution”. Same kind of people, same motivations, still hard at their evil deeds.
Best wishes
Mike

Polio wasn’t eradicated, it was renamed. Vaccines never helped. 
1824: Metal workers had suffered for centuries from a paralysis similar to polio caused by the lead and arsenic in the metals they were working with. English scientist John Cooke observed: 'The fumes from these metals, or the receptance of them in solution into the stomach, often causes paralysis.'
1890: Lead arsenate pesticide started to be sprayed in the US up to 12 times every summer to kill codling moth on apple crops.
1892: Polio outbreaks began to occur in Vermont, an apple growing region. In his report the Government Inspector Dr. Charles Caverly noted that parents reported that some children fell ill after eating fruit. He stated that 'infantile paralysis usually occurred in families with more than one child, and as no efforts were made at isolation it was very certain it was non-contagious' (with only one child in the family having been struck).
1907: Calcium arsenate comes into use primarily on cotton crops.
1908: In a Massachusetts town with three cotton mills and apple orchards, 69 children suddenly fell ill with infantile paralysis.
1909: The UK bans apple imports from the States because of heavy lead arsenate residues.
1921: Franklin D. Roosevelt develops polio after swimming in Bay of Fundy, New Brunswick. Toxicity of water may have been due to pollution run-off.
1943: DDT is introduced, a neurotoxic pesticide. Over the next several years it comes into widespread use in American households. For example, wall paper impregnated with DDT was placed in children's bedrooms.
1943: A polio epidemic in the UK town of Broadstairs, Kent is linked to a local dairy where cows were washed down with DDT.
1944: Albert Sabin reports that a major cause of sickness and death of American troops based in the Philippines was poliomyelitis. US military camps there were sprayed daily with DDT to kill mosquitoes. Neighboring Philippine settlements were not affected.
1944: NIH reports that DDT damages the same anterior horn cells that are damaged in infantile paralysis.
1946: Gebhaedt shows polio seasonality correlates with fruit harvest.
1949: Endocrinologist Dr Morton Biskind, a practitioner and medical researcher, found that DDT causes 'lesions in the spinal cord similar to human polio.'
1950: US Public Health Industrial Hygiene Medical Director, J.G. Townsend, notes the similarity between parathion poisoning and polio and believes that some polio might be caused by eating fruits or vegetables with parathion residues.
1951: Dr. Biskind treats his polio patients as poisoning victims, removing toxins from food and environment, especially DDT contaminated milk and butter. Dr. Biskind writes: 'Although young animals are more susceptible to the effects of DDT than adults, so far as the available literature is concerned, it does not appear that the effects of such concentrations on infants and children have even been considered.'

You cannot create a vaccine for a toxicity problem. You cleanse your body and live a healthier lifestyle. Why is it still on the CDC schedule? Makes a lot sense eyeroll
Big pharmaceutical and all their buddy companies and funders and fundees whatever, they don’t have our best interests at heart. Bill Gates, WHO, CDC, Anyone who thinks there should be a mandatory worldwide vaccine is full of shit and they are doing it for the money and agenda in play.


Ps: being a scientist, I wanted to test this narrative. The striking clinical claims in the postwar era would surely have been submitted to a medical journal. The people I call collectively “the perpetrators” did not yet have control of such journals.
Here’s the citation for that surprising clinical success in treating “polio” in children with high dose Vitamin C.
The scary thing is this. Someone has deleted the field normally occupied by the abstract, the short summary of the work. Generally, a good abstract sets the scene, describes what was done, the most important findings & what the implications are.
In the absence of fraud (unfortunately now sufficiently commonplace that you cannot reliably conduct a high level literature search, careful reading of well-crafted abstracts) the abstract is the “elevator pitch” of the work. I’m pretty confident that this has been removed in the recent past. It’s deletion may make it all but impossible to obtain the paper. I’m half tempted to pay the $30 or whatever it costs to obtain a full text copy.
UNLESS: do we have as readership anyone who knows how to get a copy for free? University faculty might have free literature access.
Alternatively, is their anyone skilled in searching internet archives, such as the Wayback Machine, who might get lucky and find a cached version which still contains the abstract?
Thank you 🙏
Mike

*KLENNER FR. Virus pneumonia and its treatment with vitamin C. South Med Surg. 1948 Feb;110(2):36-8. PMID: 18900646.*

💥 Less than 24hrs until THE WORLDWIDE PREMIERE of River of Freedom Film!!! 🙌

Doors to The Civic OPEN 6pm!!🎉
🎬 Be seated by 6.50pm

Most tickets are sold, grab yours NOW if you don’t wanna miss out!! ⏰

https://www.ticketmaster.co.nz/river-of-freedom-feature-documentary-auckland-premiere-auckland-05-09-2023/event/24005F0777950A1A

SPIKE PROTEIN NEWS

"The latest instalment is a finding that biological samples from about 50 per cent of mRNA vaccinees showed persisting presence of the toxic ‘spike’ protein coded by the jab, weeks or months later.  The maximum time at which it was detected was 187 days, or about six months.
It was the so-called spike protein which made the genetically engineered SARS-CoV-2 a threat to humans, through ‘gain-of-function’ experiments that converted a bat virus into the pathogen responsible for Covid-19. 
The study used a refined technique called mass spectrometry to distinguish fragments of the vaccine-encoded protein from those arising from Covid infections.
Forty subjects took part. Twenty samples were taken from vaccinated subjects, and as a control group, 20 from unvaccinated subjects who tested negative for Covid. Samples were also taken from this latter group after they contracted Covid. All still tested negative for the vaccine-associated spike, proving that the protein found in half the jab recipients was definitely specific to the jab and not Covid itself.
The study authors say there are a number of possible explanations for the persistent presence of the protein after the jab. One is the controversial idea that the genetic sequences that code for it become integrated in body cells, resulting in its continuous production. Another is that the vaccine design, which included measures to keep the sequences working much longer than naturally occurring RNA, proved far more effective than anticipated. A third is that the RNA becomes picked up by bacteria normally present in the blood.
As reported here in June, it is already known that the RNA of the Covid virus itself can make DNA sequences in a process known as reverse transcription, and that this DNA can become integrated into the cell nucleus. Researchers who demonstrated this phenomenon believe it may be responsible for puzzling observations such as positive test results in patients who have cleared all infectious virus, and perhaps also for ‘long Covid’ symptoms.
They said preliminary results suggested RNA from the vaccine does not integrate in this way. However, a study published in April showed that vials of the Pfizer and Moderna RNA jabs also contain DNA sequences, thought to be more likely to be integrated in cells because of not having to go through the reverse transcription step.
A degree of DNA contamination is inevitable due to the RNA vaccine production process, but in all cases the limits set by regulators were greatly exceeded in the samples examined.
According to the immunologist and microbiologist Dr Sucharit Bhakdi, there is no safe lower limit for the DNA. Since the jab contents, contrary to early claims, do not stay at the injection site but circulate throughout the body, there is a risk of alien DNA becoming integrated in a variety of organs and other tissues where it may continue to interfere with cell function. If the cells produce proteins that the immune system sees as foreign, the result may be a perpetual state of activation. This risks inflammatory reactions, including mycocarditis, and autoimmune diseases.
The lack of an ‘off-switch’ for dangerous antigens such as the spike protein has caused the distinguished US cardiologist Dr Peter McCullough to call for a complete moratorium of mRNA vaccine development, and for a detox regimen to break down and enable natural clearance of the spike protein. He says there is no control over where in the body the jab particles will deliver their payload. In addition, all cells that take up mRNA express foreign proteins on the cell surface, inviting an immediate auto-immune attack."

https://www.conservativewoman.co.uk/more-proof-of-the-covid-vaccine-danger/

Energy bill update

I confirm, you will not be able to dispose of, or rent your property, if you do not meet requirements that will be laid down by the Energy bill. And if you can't afford to meet those requirements and try to circumvent them, they want to send you to prison.

https://www.gov.uk/government/publications/energy-security-bill-factsheets/energy-security-bill-factsheet-power-to-review-the-energy-performance-of-buildings-regulations-energy-certificates

It’s good of Joel Smalley to point out that fair attempts were made to warn people that they were about to be attacked by injected materials which could harm them.
Wolfgang & I experienced extreme censorship, smearing and general unpleasantness, confirming we were right over the target.
It’s not a particularly good letter, and we missed a number of toxicities that are obvious to us now. Remember that at the time, the media were getting excited about how we were imminently to be saved by good works by those fantastic scientists at Pfizer, Moderna etc.

https://metatron.substack.com/p/petitionmotion-for-administrativeregulatory

You may find this interesting. A confession: we missed some toxicities that are so obvious to us now. These would have made the letter more unequivocal than it already is.
At that time, late November 2020, the media was filled with pro-vaccine stories. It was only after a sleepless night that I resolved to issue this, warts and all, the greater good definitely not being served by remaining silent in the face of near & present danger.
We were subjected to bad censorship that I wasn’t aware was even possible and also smeared everywhere including on the BBC.
Best wishes
Mike

https://metatron.substack.com/p/petitionmotion-for-administrativeregulatory

I think this is a great idea folks...

A world wide declaration we don't have to sign but can use to raise awareness about the global attack on our sovereignty and freedoms.

We can download and print these as leaflets to hand to the public!

'I am opposed to the centralization of power into the hands of unelected, unaccountable and largely unknown bureaucrats through the negotiation of international agreements that absolutely do not reflect the wishes of the people of the world.

I am opposed to what is essentially biological weapons research, regardless of whether it is referred to as vaccine research, gain-of-function research, dual use research of concern, or by any other name. This type of research must not be expanded. It must be stopped.

I am opposed to the use of terrorism and fear-mongering, including in the form of propaganda and censorship, and I am opposed to the weaponization of injectable substances that are masquerading as “vaccines” and are being pushed upon men, women and children around the world without their informed consent.

I reject the “Political Declaration of the United Nations General Assembly High-level Meeting on Pandemic Prevention, Preparedness and Response” because I do not consent to spending up to $30 billion dollars per year to “promote the fair, equitable and timely sharing of benefits arising from the use of pathogens with pandemic potential.”...'

https://jamesroguski.substack.com/p/the-peoples-declaration

#IDoNotConsent
#ExitTheWho
@FionaRoseDiamond

LONG COVID & C19 INJECTION RECOVERY PROTOCOL:

SARS-CoV-2 Base Spike Protein Detoxification in Post COVID-19 and Vaccine Injury Syndromes

"The spike protein is responsible for the pathogenicity of the SARS-CoV-2 infection and drives the development of adverse events, injuries, disabilities, and death after vaccination through immunologic and thrombotic mechanisms. The long-lasting spike protein has been found in the brain, heart, liver, kidneys, ovaries, testicles and other vital organs at autopsy in cases of death after vaccination.  In the case of vaccine-induced thrombotic injury, the spike protein has been found within the blood clot itself.  Thus, there is strong rationale for considering residual SARS-CoV-2 spike protein as a treatment target in post COVID-19 and vaccine injury syndromes. The spike protein participates directly in pathophysiology, incites inflammation, and propels thrombosis. While specific syndromes (cardiovascular, neurological, endocrine, thrombotic, immunological) will require additional therapies, we propose the clinical rationale for a base detoxification regimen of oral nattokinase, bromelain, and curcumin for patients with post-acute sequalae from SARS-CoV-2 infection and COVID-19 vaccination.
The empiric regimen can be continued for 3-12 months or more and be guided by clinical parameters:

-Nattokinase 2000 FU (100) mg orally twice a day without food

-Bromelain 500 mg orally once a day without food

-Curcumin 500 mg orally twice a day (nano, liposomal, or with piperine additive suggested)"

Peter McCullough MD

https://t.me/robinmg/30006

https://zenodo.org/record/8286460

THE "RESERVOIR" THEORY FOR LONG COVID (& C19 INJECTION):

SARS-CoV-2 reservoir in post-acute sequelae of COVID-19 (PASC)

"Replicating virus and/or viral RNA—potentially capable of being translated to produce viral proteins—persist in tissue as a ‘reservoir’. This reservoir could modulate host immune responses or release viral proteins into the circulation. Here we review studies that have identified SARS-CoV-2 RNA/protein or immune responses indicative of a SARS-CoV-2 reservoir in PASC samples. Mechanisms by which a SARS-CoV-2 reservoir may contribute to PASC pathology, including coagulation, microbiome and neuroimmune abnormalities, are delineated. "

https://www.nature.com/articles/s41590-023-01601-2