Since the declaration of the COVID-19 pandemic by the World Health Organization (WHO) on March 11, 2020, over 13.5 billion doses of COVID-19 vaccines have been administered worldwide. This remarkable achievement in vaccine distribution highlights the urgent need for comprehensive vaccine safety monitoring, as very rare adverse events associated with COVID-19 vaccines may only become apparent after widespread administration.

To address this need, the Safety Platform for Emergency Vaccines (SPEAC) initiative formulated a list of potential COVID-19 vaccine adverse events of special interest (AESI) in 2020. These AESI were selected based on various factors, including their associations with immunization, vaccine platforms, or adjuvants, as well as theoretical concerns related to immunopathogenesis.

One flexible approach for assessing AESI is the comparison of observed AESI rates following vaccine introduction with expected rates based on historical periods pre-vaccine rollout. This method, known as observed vs. expected (OE) analysis, can rapidly detect potential vaccine safety signals. For example, OE analysis played a crucial role in identifying thrombosis with thrombocytopenia syndrome (TTS) as a safety signal, prompting the suspension of the AstraZeneca COVID-19 vaccine in certain countries.

To further enhance vaccine safety monitoring, a global cohort study was conducted as part of the Global COVID Vaccine Safety (GCoVS) Project. This project, funded by the Centers for Disease Control and Prevention (CDC), involves multiple nations and aims to monitor COVID-19 vaccine safety on a global scale.

Thirteen AESI were selected for evaluation, including neurological, hematologic, and cardiovascular conditions, which are as follows:

1. Guillain-Barré syndrome (GBS),
2. Transverse myelitis (TM),
3. Facial (Bell’s) palsy,
4. Acute disseminated encephalomyelitis (ADEM), 
5. Convulsions (generalized seizures (GS), 
6. Febrile seizures (FS),
7. Cerebral venous sinus thrombosis (CVST),
8. Splanchnic vein thrombosis (SVT),
9. Pulmonary embolism (PE),
10. Thrombocytopenia,
11. Immune thrombocytopenia (ITP),
12. Myocarditis
13. Pericarditis

These conditions were chosen based on their relevance to real-world vaccine pharmacovigilance and the availability of background rates generated by GCoVS sites.

The study analyzed data from 10 sites across eight countries, comprising a total vaccinated population of 99,068,901 individuals. Notable findings include a statistically significant increase in Guillain-Barré syndrome (GBS) cases following the administration of the ChAdOx1 (India) vaccine and an increased risk of acute disseminated encephalomyelitis (ADEM) after the mRNA-1273 vaccine (Moderna).

Hematologic conditions such as cerebral venous sinus thrombosis (CVST) and immune thrombocytopenia (ITP) also showed elevated risk ratios following certain vaccine doses. Similarly, cardiovascular conditions like myocarditis and pericarditis demonstrated increased risk ratios, particularly after mRNA vaccine doses (Pfizer, Moderna, AstraZeneca).

Here is the raw data collected from the study:

Here is a chart summarizing the raw data collected in the study:

K. Faksova, et al. “COVID-19 Vaccines and Adverse Events of Special Interest: A Multinational Global Vaccine Data Network (GVDN) Cohort Study of 99 Million Vaccinated Individuals.” Vaccine, 1 Feb. 2024, https://doi.org/10.1016/j.vaccine.2024.01.100.

The documentary "War on Ivermectin" explores the contentious landscape surrounding the drug Ivermectin during the COVID-19 pandemic. It delves into the controversy surrounding the use of Ivermectin as a potential treatment for COVID-19 and the challenges it has faced from regulatory bodies and mainstream medical establishments.

The documentary presents perspectives from advocates of Ivermectin, who argue for its efficacy and safety in treating COVID-19. It may shed light on the resistance faced by proponents of Ivermectin, exploring factors such as media portrayal, regulatory decisions, and the broader implications for the treatment landscape.
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Additionally, the documentary might feature interviews with medical professionals, researchers, and individuals who have been affected by the debate over Ivermectin. It aims to provide a comprehensive overview of the complex and polarized discussions surrounding the drug in the context of the global response to the pandemic.

Safe and Effective: A Second Opinion shines a light on Covid-19 vaccine injuries and bereavements, but also takes an encompassing look at the systemic failings that appear to have enabled them. We look at leading analysis of pharmaceutical trials, the role of the MHRA in regulating these products, the role of the SAGE behavioural scientists in influencing policy and the role of the media and Big Tech companies in supressing free and open debate on the subject.

Mitch Butler and Josh Landis discussed how germs and viruses have shaped our bodies and even our DNA throughout history.

In this episode of The Highwire, Del Bigtree highlights the Medical Freedom Movement Makes History; Freedom Convoy Exploding in Canada; Catastrophic New Covid Vaccine Data; Del’s Message to a Manic Mainstream Media; and Experts Second Opinion on The Pandemic. 
Guest: Dr. Richard Urso

In this episode of The Highwire, Del Bigtree highlights The War on Pro Athletes; Ethics Expert Fired Over Mandate; Vaccine’s Flopping Against Omicron; New Docs Expose Fauci; ICAN Landmark Wins & Critique of SCOTUS Hearing.
Guests: Jonathan Isaac, Aaron Kheriaty M.D., Aaron Siri, Esq.

In this episode of The Highwire, Del Bigtree highlights A Look Back on HighWire’s Coverage of Covid; Welcome to the Party, Joe Rogan; ICAN Sues for V-Safe Data; Are You Suffering From Mass Delusional Psychosis?; and COVID Deaths Down, excess Deaths up? Are Government Payouts Manipulating US Covid Data?
Guests: Dr. Mark McDonald, AJ DePriest

In this episode of The Highwire, Del Bigtree highlights Firemen Fight for Freedom; British Mathematician Uncovers Disturbing UK Death Data; What is Wrong with Omicron?; Hospital Won’t Admit Tragic Vaccine Death?; and Big Pharma’s Faithful Jumping Ship
GUESTS: Fireman John Knox, Prof. Norman Fenton, Gina Doane, Deb Conrad, PA-C

In this episode of The Highwire, Del Bigtree highlights, FDA to Disclose Pfizer Data...in 56 years?!; Biden’s Mandate On Hold; CDC Whiffs On Natural Immunity; and Vaccine Expert’s Dire Mass Covid Vaccination Warning
Guests: Aaron Siri, Esq., Geert Vanden Bossche, PhD, DVM

In this episode of The Highwire, Del Bigtree highlights Big Bird Gets Covid Shot; Aaron Rodgers Throws Covid Touchdown; Homeschooling 101; Disruption of our DNA & Other Sins of ScienceGuests: Dana & Chelsea Broussard, Sam Sorbo

In this episode of The Highwire, Del Bigtree highlights D.C. Panel Highlights Vaccine Injuries; CDC Approves Covid Shot for Kids; Conflicting Data on Myocarditis in Kids; and America Stages Walkout
GUESTS: Brianne Dressen, Peter McCullough MD, Leigh Dundas, Esq.

In this episode of The HighWire featuring Del Bigtree, the discussion covers a range of critical topics, providing insights into the current state of affairs. The episode begins by addressing the concerns of growing tyranny in Australia, highlighting the challenging situations faced by the residents. Delving into the NBA standoff, the episode sheds light on the contentious issue surrounding vaccination requirements and the stance taken by players.

A significant segment of the episode focuses on the widespread job terminations due to vaccine mandates, with thousands facing the consequences of these policies. The 'Rome Declaration' gains attention as 7,200 individuals sign this new declaration, indicating a growing movement for vaccine choice and personal freedom.

The precarious situation faced by a New York restaurant under threat due to vaccine-related regulations is explored, exemplifying the challenges businesses encounter in navigating these uncertain times. The episode also features a meeting between two prominent figures in the COVID landscape, offering valuable perspectives on the ongoing situation.
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Guests Taylor and Frank Winterstein, Irene Siderakis, and Deborah Conrad, PA-C contribute to the discussion, providing expert insights and sharing their experiences. The overarching themes of Covid Giants, Vaccine Choice, the Rome Declaration, BidensBooster, and the VAERS Whistleblower underscore the episode's commitment to addressing pressing issues and fostering informed discussions around these critical topics.

In this episode of The Highwire, Del breaks an exclusive newly-unredacted bombshell Fauci email; Dr. Jeffery Barke tells us why not to buy into Delta fears; CDC lying about natural immunity; Former Federal Official Catherine Austin Fitts’ urgent warning for all Americans.

Dr. Peter McCullough, joins the Highwire again, this time to discuss the serious problem with the efficacy of the COVID-19 vaccines and how mass vaccination is creating this runaway train of a pandemic. In this episode, Del and Dr. McCullough talk about vaccine efficacy, the delta variant, natural immunity, and asymmetric reporting, among other topics. 

Geert Vanden Bossche, PhD, DVM, is an internationally recognized vaccine research expert and developer. He has a long list of companies and organizations he’s worked with on vaccine discovery and preclinical research, including the head of the Vaccine Development Office at the German Centre for Infection Research, GSK, Novartis, Solvay Biologicals, and Bill & Melinda Gates Foundation. Dr Vanden Bossche also coordinated the Ebola vaccine program at GAVI (Global Alliance for Vaccines and Immunization) and contributed to the implementation of an integrated vaccine work plan in collaboration with Global Health Partners (WHO, Bill & Melinda Gates Foundation, CDC, UNICEF), regulators (FDA) and vaccine manufacturers to enable timely deployment or stockpiling of Ebola vaccine candidates.

He is board-certified in Virology and Microbiology, the author of over 30 publications, and inventor of a patent application for universal vaccines. He currently works as an independent vaccine research consultant. In this following video, he shares his perspective on mass vaccination of SARS-CoV2, and highlights the principle of using a prophylactic vaccine in the midst of a pandemic, which is likely to create more viral variants in the process.

Bossche states that the multiple emerging, “much more infectious” viral variants, are already examples of “immune escape” from our ‘innate immunity’, and were most-likely created by the government interventions themselves; the so-called Non-Pharmacological Interventions (NPIs) – i.e. lockdowns and cloth facial coverings. Unofficially, but also more aptly known as the Non-Scientific Interventions.
He believes that:

• Ongoing mass vaccination deployments are “highly-likely to further enhance ‘adaptive’ immune escape as none of the current vaccines will prevent replication/transmission of viral variants”
• As such, “The more we use these vaccines for immunizing people in the midst of a pandemic, the more infectious the virus will become”.
• And “With increasing infectiousness comes an increased likelihood of viral resistance to the vaccines”.

He claims his beliefs are basic principles taught in a student’s first vaccinology class – “One shouldn’t use a prophylactic vaccine in populations exposed to high infectious pressure (which is now certainly the case as multiple highly infectious variants are currently circulating”).
He states that to “fully escape”, the highly mutable virus, “only needs to add another few mutations in its receptor-binding domain”.

​Below is his open letter to the WHO, issued March 6th, 2021.

​Geert Vanden Bossche, DMV, PhD, independent virologist and vaccine expert, formerly employed at GAVI and The Bill & Melinda Gates Foundation.

​To all authorities, scientists and experts around the world, to whom this concerns: the entire world population.

I am all but an antivaxxer. As a scientist I do not usually appeal to any platform of this kind to make a stand on vaccine-related topics. As a dedicated virologist and vaccine expert I only make an exception when health authorities allow vaccines to be administered in ways that threaten public health, most certainly when scientific evidence is being ignored. The present extremely critical situation forces me to spread this emergency call. As the unprecedented extent of human intervention in the Covid-19- pandemic is now at risk of resulting in a global catastrophe without equal, this call cannot sound loudly and strongly enough.

As stated, I am not against vaccination. On the contrary, I can assure you that each of the current vaccines have been designed, developed and manufactured by brilliant and competent scientists. However, this type of prophylactic vaccines are completely inappropriate, and even highly dangerous, when used in mass vaccination campaigns during a viral pandemic. Vaccinologists, scientists and clinicians are blinded by the positive short-term effects in individual patents, but don’t seem to bother about the disastrous consequences for global health. Unless I am scientifically proven wrong, it is difficult to understand how current human interventions will prevent circulating variants from turning into a wild monster.

Racing against the clock, I am completing my scientific manuscript, the publication of which is, unfortunately, likely to come too late given the ever increasing threat from rapidly spreading, highly infectious variants. This is why I decided to already post a summary of my findings as well as my keynote speech at the recent Vaccine Summit in Ohio on LinkedIn. Last Monday, I provided international health organizations, including the WHO, with my analysis of the current pandemic as based on scientifically informed insights in the immune biology of Covid-19. Given the level of emergency, I urged them to consider my concerns and to initiate a debate on the detrimental consequences of further ‘viral immune escape’. For those who are no experts in this field, I am attaching below a more accessible and comprehensible version of the science behind this insidious phenomenon.

​While there is no time to spare, I have not received any feedback thus far. Experts and politicians have remained silent while obviously still eager to talk about relaxing infection prevention rules and 'springtime freedom'. My statements are based on nothing else but science. They shall only be contradicted by science. While one can barely make any incorrect scientific statements without being criticized by peers, it seems like the elite of scientists who are currently advising our world leaders prefer to stay silent. Sufficient scientific evidence has been brought to the table. Unfortunately, it remains untouched by those who have the power to act. How long can one ignore the problem when there is at present massive evidence that viral immune escape is now threatening humanity? We can hardly say we didn't know - or were not warned.

In this agonizing letter I put all of my reputation and credibility at stake. I expect from you, guardians of mankind, at least the same. It is of utmost urgency. Do open the debate. By all means: turn the tide!

PUBLIC HEALTH EMERGENCY OF INTERNATIONAL CONCERN
Why mass vaccination amidst a pandemic creates an irrepressible monster
THE key question is: why does nobody seem to bother about viral immune escape? Let me try to explain this by means of a more easily understood phenomenon: Antimicrobial resistance. One can easily extrapolate this scourge to resistance to our self-made ‘antiviral antibiotics’. Indeed, antibodies (Abs) produced by our own immune system can be considered self-made antiviral antibiotics, regardless of whether they are part of our innate immune system (so-called ‘natural’ Abs’) or elicited in response to specific pathogens (resulting in so-called ‘acquired’ Abs). Natural Abs are not germ-specific whereas acquired Abs are specifically directed at the invading pathogen. At birth, our innate immune system is ‘unexperienced’ but well-established. It protects us from a multitude of pathogens, thereby preventing these pathogens from causing disease. As the innate immune system cannot remember the pathogens it encountered (innate immunity has no so-called ‘immunological memory’), we can only continue to rely on it provided we keep it ‘trained’ well enough. Training is achieved by regular exposure to a myriad of environmental agents, including pathogens. However, as we age, we will increasingly face situations where our innate immunity (often called ‘the first line of immune defense’) is not strong enough to halt the pathogen at the portal of entry (mostly mucosal barriers like respiratory or intestinal epithelia). When this happens, the immune system has to rely on more specialized effectors of our immune system (i.e., antigen-specific Abs and T cells) to fight the pathogen. So, as we grow up, we increasingly mount pathogen-specific immunity, including highly specific Abs. As those have stronger affinity for the pathogen (e.g., virus) and can reach high concentrations, they can quite easily outcompete our natural Abs for binding to the pathogen/virus. It is precisely this type of highly specific, high affinity Abs that current Covid-19 vaccines are inducing. Of course, the noble purpose of these Abs is to protect us against Covid-19. So, why then should there be a major concern using these vaccines to fight Covid-19?

Well, similar to the rules applying to classical antimicrobial antibiotics, it is paramount that our self-made ‘antiviral antibiotics’ are made available in sufficient concentration and are tailored at the specific features of our enemy. This is why in case of bacterial disease it is critical to not only chose the right type of antibiotic (based on the results from an antibiogram) but to also take the antibiotic for long enough (according to the prescription). Failure to comply with these requirements is at risk of granting microbes a chance to survive and hence, may cause the disease to fare up. A very similar mechanism may also apply to viruses, especially to viruses that can easily and rapidly mutate (which is, for example, the case with Coronaviruses); when the pressure exerted by the army’s (read: population’s) immune defense starts to threaten viral replication and transmission, the virus will take on another coat so that it can no longer be easily recognized and, therefore, attacked by the host immune system. The virus is now able to escape immunity (so-called: ‘immune escape’). However, the virus can only rely on this strategy provided it still has room enough to replicate. Viruses, in contrast to the majority of bacteria, must rely on living host cells to replicate. This is why the occurrence of ‘escape mutants’ isn’t too worrisome as long as the likelihood for these variants to rapidly find another host is quite remote. However, that’s not particularly the case during a viral pandemic! During a pandemic, the virus is spreading all over the globe with many subjects shedding and transmitting the virus (even including asymptomatic ‘carriers’). The higher the viral load, the higher the likelihood for the virus to bump into subjects who haven’t been infected yet or who were infected but didn’t develop symptoms. Unless they are sufficiently protected by their innate immune defense (through natural Abs), they will catch Covid-19 disease as they cannot rely on other, i.e., acquired Abs. It has been extensively reported, indeed, that the increase in S (spike)-specific Abs in asymptomatically infected people is rather limited and only short-lived. Furthermore, these Abs have not achieved full maturity. The combination of viral infection on a background of suboptimal Ab maturity and concentration enables the virus to select mutations allowing it to escape the immune pressure. The selection of those mutations preferably occurs in the S protein as this is the viral protein that is responsible for viral infectiousness. As the selected mutations endow the virus with increased infectious capacity, it now becomes much easier for the virus to cause severe disease in infected subjects. The more people develop symptomatic disease, the better the virus can secure its propagation and perpetuation (people who get severe disease will shed more virus and for a longer period of time than asymptomatically infected subjects do). Unfortunately enough, the short-lived rise in S-specific Abs does, however, suffice to bypass people’s innate/natural Ab. Those are put out of business as their affinity for S is lower than the affinity of S-specific Abs. This is to say that with an increasing rate of infection in the population, the number of subjects who get infected while experiencing a momentary increase in Specific Abs will steadily increase. Consequently, the number of subjects who get infected while experiencing a momentary decrease in their innate immunity will increase. As a result, a steadily increasing number of subjects will become more susceptible to getting severe disease instead of showing only mild symptoms (i.e., limited to the upper respiratory tract) or no symptoms at all. During a pandemic, especially youngsters will be affected by this evolution as their natural Abs are not yet largely suppressed by a panoply of ‘acquired’, antigen-specific Abs. Natural Abs, and natural immunity in general, play a critical role in protecting us from pathogens as they constitute our first line of immune defense. In contrast to acquired immunity, innate immune responses protect against a large spectrum of pathogens (so don’t compromise or sacrifice your innate immune defense!). Because natural Abs and innate immune cells recognize a diversified spectrum of foreign (i.e., non-self) agents (only some of which have pathogenic potential), it’s important, indeed, to keep it sufficiently exposed to environmental challenges. By keeping the innate immune system (which, unfortunately, has no memory!) TRAINED, we can much more easily resist germs which have real pathogenic potential. It has, for example, been reported and scientifically proven that exposure to other, quite harmless Coronaviruses causing a ‘common cold ’ can provide protection, although short-lived, against Covid-19 and its loyal henchmen (i.e., the more infectious variants).

​Suppression of innate immunity, especially in the younger age groups, can, therefore, become very problematic. There can be no doubt that lack of exposure due to stringent containment measures implemented as of the beginning of the pandemic has not been beneficial to keeping people’s innate immune system well trained. As if this was not already heavily compromising innate immune defense in this population segment, there comes yet another force into play that will dramatically enhance morbidity and mortality rates in the younger age groups: MASS VACCINATION of the ELDERLY. The more extensively the later age group will be vaccinated and hence, protected, the more the virus is forced to continue causing disease in younger age groups. This is only going to be possible provided it escapes to the S-specific Abs that are momentarily raised in previously asymptomatically infected subjects. If the virus manages to do so, it can benefit from the (momentarily) suppressed innate immunity, thereby causing disease in an increasing number of these subjects and ensuring its own propagation. Selecting targeted mutations in the S protein is, therefore, the way to go in order for the virus to enhance its infectiousness in candidates that are prone to getting the disease because of a transient weakness of their innate immune defense.

​But in the meantime, we’re also facing a huge problem in vaccinated people as they’re now more and more confronted with infectious variants displaying a type of S protein that is increasingly different from Author: Geert Vanden Bossche, DVM, PhD (March 6, 2021) – https://www.linkedin.com/in/geertvandenbossche/ the S edition comprised with the vaccine (the later edition originates from the original, much less infectious strain at the beginning of the pandemic). The more variants become infectious (i.e., as a result of blocking access of the virus to the vaccinated segment of the population), the less vaccinal Abs will protect. Already now, lack of protection is leading to viral shedding and transmission in vaccine recipients who are exposed to these more infectious strains (which, by the way, increasingly dominate the field). This is how we are currently turning vaccines into asymptomatic carriers shedding infectious variants.

At some point, in a likely very near future, it’s going to become more profitable (in term of ‘return on selection investment’) for the virus to just add another few mutations (maybe just one or two) to the S protein of viral variants (already endowed with multiple mutations enhancing infectiousness) in an attempt to further strengthen its binding to the receptor (ACE-2) expressed on the surface of permissive epithelial cells. This will now allow the new variant to outcompete vaccinal Abs for binding to the ACE receptor. This is to say that at this stage, it would only take very few additional targeted mutations within the viral receptor-binding domain to fully resist specific anti-Covid-19 Abs, regardless whether the later are elicited by the vaccine or by natural infection. At that stage, the virus will, indeed, have managed to gain access to a huge reservoir of subjects who have now become highly susceptible to disease as their S-specific Abs have now become useless in terms of protection but still manage to provide for long-lived suppression of their innate immunity (i.e., natural infection, and especially vaccination, elicit relatively long-lived specific Ab titers). The susceptible reservoir comprises both, vaccinated people and those who’re left with sufficient S-specific Abs due to previous Covid-19 disease). So, MISSION ACCOMPLISHED for Covid-19 but a DISASTROUS SITUATION for all vaccinated subjects and Covid-19 seropositive people as they’ve now lost both, their acquired and innate immune defense against Covid-19 (while highly infectious strains are circulating!). That’s ‘one small step for the virus, one giant catastrophe for mankind’, which is to say that we’ll have whipped up the virus in the younger population up to a level that it now takes little effort for Covid-19 to transform into a highly infectious virus that completely ignores both the innate arm of our immune system as well as the adaptive/acquired one (regardless of whether the acquired Abs resulted from vaccination or natural infection). The effort for the virus is now becoming even more negligible given that many vaccine recipients are now exposed to highly infectious viral variants while having received only a single shot of the vaccine. Hence, they are endowed with Abs that have not yet acquired optimal functionality. There is no need to explain that this is just going to further enhance immune escape. Basically, we’ll very soon be confronted with a super-infectious virus that completely resists our most precious defense mechanism: The human immune system. From all of the above, it’s becoming increasingly difficult to imagine how the consequences of the extensive and erroneous human intervention in this pandemic are not going to wipe out large parts of our human population. One could only think of very few other strategies to achieve the same level of efficiency in turning a relatively harmless virus into a bioweapon of mass destruction. It’s certainly also worth mentioning that mutations in the S protein (i.e., exactly the same protein that is subject to selection of escape mutations) are known to enable Coronaviruses to cross species barriers. This is to say that the risk that vaccine-mediated immune escape could allow the virus to jump to other animal species, especially industrial livestock (e.g., pig and poultry farms), is not negligible. These species are already known to host several different Coronaviruses and are usually housed in farms with high stocking density. Similar to the situation with influenza virus, these species could than serve as an additional reservoir for SARS-COVID-2 virus.

As pathogens have co-evolved with the host immune system, natural pandemics of acute self-limiting viral infections have been shaped such as to take a toll on human lives that is not higher than strictly required. Due to human intervention, the course of this pandemic has been thoroughly disturbed as of the very beginning. Widespread and stringent infection prevention measures combined with mass vaccination campaigns using inadequate vaccines will undoubtedly lead to a situation where the pandemic is getting increasingly ‘out of control’.

​Paradoxically, the only intervention that could offer a perspective to end this pandemic (other than to let it run its disastrous course) is …VACCINATION. Of course, the type of vaccines to be used would be completely different of conventional vaccines in that they’re not inducing the usual suspects, i.e., B and T cells, but NK cells. There is, indeed, compelling scientific evidence that these cells play a key role in facilitating complete elimination of Covid-19 at an early stage of infection in symptomatically infected subjects. NK cells are part of the cellular arm of our innate immune system and, alike natural Abs, they are capable of recognizing and attacking a broad and diversified spectrum of pathogenic agents. There is a sound scientific rationale to assume that it is possible to ‘prime’ NK cells in ways for them to recognize and kill Coronaviruses at large (include all their variants) at an early stage of infection. NK cells have increasingly been described to be endowed with the capacity to acquire immunological memory. By educating these cells in ways that enable them to durably recognize and target Coronavirus-infected cells, our immune system could be perfectly armed for a targeted attack to the universe of Coronaviruses prior to exposure. As NK cell-based immune defense provides sterilizing immunity and allows for broadspectrum and fast protection, it is reasonable to assume that harnessing our innate immune cells is going to be the only type of human intervention left to halt the dangerous spread of highly infectious Covid-19 variants.

If we, human beings, are committed to perpetuating our species, we have no choice left but to eradicate these highly infectious viral variants. This will, indeed, require large vaccination campaigns. However, NK cell-based vaccines will primarily enable our natural immunity to be better prepared (memory!) and to induce herd immunity (which is exactly the opposite of what current Covid-19 vaccines do as those increasingly turn vaccine recipients into asymptomatic carriers who are shedding virus). So, there is not one second left for gears to be switched and to replace the current killer vaccines by life-saving vaccines.

I am appealing to the WHO and all stakeholders involved, no mater their conviction, to immediately declare such acton as THE SINGLE MOST IMPORTANT PUBLIC HEALTH EMERGENCY OF INTERNATIONAL CONCERN.

CDC Spin on New Mask Data; Celebrity Catches Fauci Lying!; Expert Warns of Coming Covid Vaccine Disaster; Hell in the Holy Land

Dr. David Martin, founder and chairman of M-CAM Inc, challenges our presuppositions about the new mRNA Covid-19 vaccines. Quoting the pharmaceutical companies themselves, David suggests that these are not vaccines, but, in actuality, gene therapy. He explains what the vaccines may do to us, what they are promising they can do for us, and how to distinguish the difference.

AFLDS founder Simone Gold, MD, JD, FABEM, “the doctor who went viral,” is a board-certified emergency physician and author of the best-selling book “I Do Not Consent: My Fight Against Medical Cancel Culture.” She graduated from Chicago Medical School before attending Stanford University Law School to earn her Juris Doctorate degree. Dr. Gold worked in Washington, D.C. for the Surgeon General, as well as for the Chairman of the U.S. Senate Labor and Human Resources Committee.
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Dr. Gold is a frequent guest on media outlets across the country. She has appeared in USA Today, the Associated Press, the Guardian (UK), New York Times, and many other publications. She has been featured on such nationally syndicated programs as The Tucker Carlson Show, The Ingraham Angle, The Glenn Beck Show, The Charlie Kirk Show, The Dennis Prager Show, Day Star Television, and others. In July 2020, she organized the first-ever America’s Frontline Doctors White Coat Summit in Washington, D.C., which drew 20 million views online. Dr. Gold is America’s leading voice of common sense and scientific clarity in the fight against COVID-19.

Zach Bush MD is a physician specializing in internal medicine, endocrinology and hospice care. He is an internationally recognized educator and thought leader on the microbiome as it relates to health, disease, and food systems. Dr Zach founded Seraphic Group and the nonprofit Farmer’s Footprint to develop root-cause solutions for human and ecological health. His passion for education reaches across many disciplines, including topics such as the role of soil and water ecosystems in human genomics, immunity, and gut/brain health. His education has highlighted the need for a radical departure from chemical farming and pharmacy, and his ongoing efforts are providing a path for consumers, farmers, and mega-industries to work together for a healthy future for people and planet.

Show Notes

• A trip to the Philippines changed Zack’s life mission and how he viewed allopathic medicine afterward. (10:07)
• “The scientific method is nothing more than a technique for exploring truth, but at no point is science a body of knowledge or truth…” (28:16)
• Zach’s bedrock spiritual philosophy: I am. (41:06)
• Homo sapiens is an adaptive species and not a stagnant one. (55:09)
• What’s the difference between a rishi and a reishi mushroom? (1:14:00)
• A quantum physics fellowship. (1:23:20)
• Healing relationships at death’s door. (1:36:32)
• Random event generators and the death of George Floyd. (1:40:15)
• Do humans have the raw potential to co-create something magnificent? (1:50:21)

Resources

• Zack’s articles co-written with Deepak Chopra on June 1 and June 8 in the SF Gate
• Antoine Béchamp vs. Louis Pasteur
• The work of J.R.R. Tolkien and John Archibald Wheeler
• Mycorrhiza
• Superstring theory
• The Abdominal and Pelvic Brain by Byron Robinson
• Intestinal Gardening for the Prolongation of Youth by James Empringham
• Universal Sufism by H.J. Witteveen and Scott Sattler
• Streams of Wisdom by Dustin DiPerna and Ken Wilbur

In this conversation, Dr. Tom Cowan and Sally Fallon Morrell discuss The Contagion Myth. 

The official explanation for today’s COVID-19 pandemic is a “dangerous, infectious virus.” This is the rationale for isolating a large portion of the world’s population in their homes so as to curb its spread. From face masks to social distancing, from antivirals to vaccines, these measures are predicated on the assumption that tiny viruses can cause serious illness and that such illness is transmissible person-to-person.

It was Louis Pasteur who convinced a skeptical medical community that contagious germs cause disease; his “germ theory” now serves as the official explanation for most illness. However, in his private diaries, he states unequivocally that in his entire career he was not once able to transfer disease with a pure culture of bacteria (he obviously wasn’t able to purify viruses at that time). He admitted that the whole effort to prove contagion was a failure, leading to his famous death bed confession that “the germ is nothing, the terrain is everything.” 

While the incidence and death statistics for COVID-19 may not be reliable, there is no question that many people have taken sick with a strange new disease—with odd symptoms like gasping for air and “fizzing” feelings—and hundreds of thousands have died. Many suspect that the cause is not viral but a kind of pollution unique to the modern age—electromagnetic pollution. Today we are surrounded by a jangle of overlapping and jarring frequencies—from power lines to the fridge to the cell phone. It started with the telegraph and progressed to worldwide electricity, then radar, then satellites that disrupt the ionosphere, then ubiquitous Wi-Fi. The most recent addition to this disturbing racket is fifth-generation wireless—5G. In The Contagion Myth: Why Viruses (including Coronavirus) are Not the Cause of Disease, bestselling authors Thomas S. Cowan, MD, and Sally Fallon Morell tackle the true causes of COVID-19.

On September 26, 2019, 5G wireless was turned on in Wuhan, China (and officially launched November 1) with a grid of about ten thousand antennas—more antennas than exist in the whole United States, all concentrated in one city. A spike in cases occurred on February 13, the same week that Wuhan turned on its 5G network for monitoring traffic. Illness has subsequently followed 5G installation in all the major cities in America.
​
Since the dawn of the human race, medicine men and physicians have wondered about the cause of disease, especially what we call “contagions,” numerous people ill with similar symptoms, all at the same time. Does humankind suffer these outbreaks at the hands of an angry god or evil spirit? A disturbance in the atmosphere, a miasma? Do we catch the illness from others or from some outside influence?

As the restriction of our freedoms continues, more and more people are wondering whether this is true. Could a packet of RNA fragments, which cannot even be defined as a living organism, cause such havoc? Perhaps something else is involved—something that has upset the balance of nature and made us more susceptible to disease? Perhaps there is no “coronavirus” at all; perhaps, as Pasteur said, “the germ is nothing, the terrain is everything.”

From RT:

​Now, we have a thing called a messenger RNA vaccine (mRNA). RNA is, effectively, a single strand of DNA – the double helix that sits within our cells and makes up our genetic code. Many viruses are made up of a single strand of RNA, surrounded by a protein sphere.
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They enter the cell, take over the replication systems, make thousands of copies of themselves, then exit the cell. Sometimes killing the cell as they do so, sometimes exiting more gently. Covid19 (Sars-Cov2) is an RNA virus.

Knowing this, rather than attempting to create a weakened virus, which can take years, or break the virus into bits, the vaccine researchers decided to use Sars-Cov2’s RNA against itself. To do this, they isolated the section of RNA which codes for the ‘spike’ protein – which is the thing the virus uses as a ‘key’ to enter cells. 

They then worked out how to insert this small section of RNA, messenger RNA, into the cell, where it takes over a part of the protein replication mechanisms that sit inside all cells. They turn the mechanism into a 3D printer, churning out copies of the spike protein.

These spike proteins then leave the cell – somehow or other, this bit is unclear. The immune system comes across them, recognises them as ‘alien’ and attacks. In doing so, antibodies are created, and the immune memory system kicks into action. If, later on, a Sars-Cov2 virus gets into the body, the immune system fires up and attacks the remembered spike protein. Hopefully killing the entire virus.

This is all, certainly very clever stuff. What, as they say, could possibly go wrong?

The first thing to say is that, with something this new, we don’t really know. It could be that it is absolutely 100 percent safe. We are told that none of the mRNA can get into the nucleus of the cell, where it could become incorporated into the DNA. I hope so. Could it trigger an immune cascade? I hope not.
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I know that the researchers will be looking very, very, closely at the novel safety issues that could emerge. If they are not, they damned well should be. However, the timelines here are very short. It normally takes many years to create safe and effective vaccines. Here is it happening in, effectively, weeks.

Before his death, the inventor of the PCR test, Kary Mullis, repeatedly yet unsuccessfully stressed that this test should not be used as a diagnostic tool for the simple reason that it's incapable of diagnosing disease. A positive test does not actually mean that an active infection is present. As noted in a U.S. Centers for Disease Control and prevention publication on coronavirus and PCR testing dated July 13 2020:2

• Detection of viral RNA may not indicate the presence of infectious virus or that 2019-nCoV is the causative agent for clinical symptoms.
• The performance of this test has not been established for monitoring treatment of 2019-nCoV infection.
• This test cannot rule out diseases caused by other bacterial or viral pathogens.

So, what does the PCR test actually tell us? The PCR swab collects RNA from your nasal cavity. This RNA is then reverse transcribed into DNA. However, the genetic snippets are so small they must be amplified in order to become discernible. Each round of amplification is called a cycle.

Amplification over 35 cycles is considered unreliable and scientifically unjustified, yet Drosten tests and tests recommended by the World Health Organization are set to 45 cycles.

What this does is amplify any, even insignificant sequences of viral DNA that might be present to the point that the test reads "positive," even if the viral load is extremely low or the virus is inactive. As a result of these excessive cycle thresholds, you end up with a far higher number of positive tests than you would otherwise.

We've also had problems with faulty and contaminated tests. As soon as the genetic sequence for SARS-CoV-2 became available in January 2020, German researchers quickly developed a PCR test for the virus.
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In March 2020, The New York Times3 reported the initial test kits developed by the CDC had been found to be flawed. The Verge also reported4 that this flawed CDC test in turn became the basis for the WHO's test, which the CDC ended up refusing to use.

Perhaps most importantly of all, the PCR tests cannot distinguish between inactive viruses and "live" or reproductive ones. What that means is that PCR tests cannot detect infection. Period. It cannot tell you whether you're currently ill, whether you'll develop symptoms in the near future, or whether you're contagious.

The tests may pick up dead debris or inactive viral particles that pose no risk whatsoever to the patient and others. What's more, the test can pick up the presence of other coronaviruses, so a positive result may simply indicate that you've recuperated from a common cold in the past.

An "infection" is when a virus penetrates into a cell and replicates. As the virus multiplies, symptoms set in. A person is only infectious if the virus is actually replicating. As long as the virus is inactive and not replicating, it's completely harmless both to the host and others.

Chances are, if you have no symptoms, a positive test simply means it has detected inactive viral DNA in your body. This would also mean that you are not contagious and pose no risk to anyone.

For all of these reasons, a number of highly respected scientists around the world are now saying that what we have is not a COVID-19 pandemic but a PCR test pandemic. In his September 20, 2020, article5 "Lies, Damned Lies and Health Statistics — The Deadly Danger of False Positives," Yeadon explains why basing our pandemic response on positive PCR tests is so problematic.
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In short, it appears millions of people are simply being found to carry inactive viral DNA that pose no risk to anyone, yet these test results are being used by the global technocracy to implement a brand new economic and social system based on draconian surveillance and totalitarian controls.

Perhaps most importantly of all, the PCR tests cannot distinguish between inactive viruses and "live" or reproductive ones. What that means is that PCR tests cannot detect infection. Period. It cannot tell you whether you're currently ill, whether you'll develop symptoms in the near future, or whether you're contagious.

The tests may pick up dead debris or inactive viral particles that pose no risk whatsoever to the patient and others. What's more, the test can pick up the presence of other coronaviruses, so a positive result may simply indicate that you've recuperated from a common cold in the past.
​
An "infection" is when a virus penetrates into a cell and replicates. As the virus multiplies, symptoms set in. A person is only infectious if the virus is actually replicating. As long as the virus is inactive and not replicating, it's completely harmless both to the host and others.

Chances are, if you have no symptoms, a positive test simply means it has detected inactive viral DNA in your body. This would also mean that you are not contagious and pose no risk to anyone.
​
For all of these reasons, a number of highly respected scientists around the world are now saying that what we have is not a COVID-19 pandemic but a PCR test pandemic. In his September 20, 2020, article5 "Lies, Damned Lies and Health Statistics — The Deadly Danger of False Positives," Yeadon explains why basing our pandemic response on positive PCR tests is so problematic.

In short, it appears millions of people are simply being found to carry inactive viral DNA that pose no risk to anyone, yet these test results are being used by the global technocracy to implement a brand new economic and social system based on draconian surveillance and totalitarian controls.

As reported by The Vaccine Reaction, September 29, 2020:6

"The test's threshold is so high that it detects people with the live virus as well as those with a few genetic fragments left over from a past infection that no longer poses a risk. It's like finding a hair in a room after a person left it, says Michael Mina, MD, an epidemiologist at the Harvard T.H. Chan School of Public Health.7

In three sets of testing data that include cycle thresholds compiled by officials in Massachusetts, New York and Nevada, up to 90% of people testing positive carried barely any virus, a review by The New York Times found8 …

'We've been using one type of data for everything, and that is just plus or minus — that's all,' Dr. Mina said. 'We're using that for clinical diagnostics, for public health, for policy decision-making.'

But 'yes' or 'no' isn't good enough, he added. It's the amount of virus that should dictate the infected patient's next steps. 'It's really irresponsible, I think, to forgo the recognition that this is a quantitative issue,' Dr. Mina said."

Again, medical experts agree any cycle threshold over 35 cycles makes the test too sensitive, as at that point it starts picking up harmless inactive DNA fragments. Mina believes a more reasonable cutoff would be 30 or less.

As noted by Dr. Tom Jefferson and professor Carl Henegan in an October 31, 2020, article in the Daily Mail,16 mass PCR testing has been a massive waste or resources, as it doesn't provide us with the information we actually need to know — who's infectious, how far is the virus spreading and how fast does it spread?

Instead, it has led to economic devastation from business shutdowns and isolating noninfectious people in their homes for weeks and months on end. Jefferson and Henegan claim they shared their pandemic response plan with British Prime Minister Boris Johnson over a month ago, and just presented it to him again. "We urge him to pay attention and embrace it," they write, adding:

"There are only two things about which we can be certain: first, that lockdowns do not work in the long term … The idea that a month of economic hardship will permit some sort of 'reset', allowing us a brighter future, is a myth. What, when it ends, do we think will happen? Meanwhile, ever-increasing restrictions will destroy lives and livelihoods.

The second certainty is this: that we need to find a way out of the mess that does no more damage than the virus itself … Our strategy would be to tackle the four key failings."

These four areas are:

1. Addressing the problems in the government's mass testing program
2. Addressing "the blight of confused and contradictory statistics"
3. Protect and isolate the vulnerable — primarily the elderly, but also hospitalized patients in general and staff — while allowing the rest to maintain "some semblance of normal life"
4. Inform the public about the true and quantifiable costs of lockdown that "kill people just as surely as COVID-19"

"If we do these things, there is real hope that we can learn to live with the virus. That, after all, was supposed to be the plan," Jefferson and Henegan note. With regard to testing, the pair call "for a national program of testing quality control to ensure that results are accurate, precise and consistent."
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Importantly, we must not rely on positive/negative readings alone. The results must be assessed in relation to other factors, such as the age of the subject and whether they are symptomatic, to determine who actually poses an infectious risk. You can review the full details of their proposed plan at the end of their Daily Mail article.17

Jefferson and Henegan aren't the only ones highlighting the fact that the global lockdown strategy is causing more harm and destruction than the virus itself. In a June 16, 2020 article in The Federalist, James Lucas, a New York City attorney, wrote:18

"If we're going to allow models and modelers to dictate the entire nature of our society, one would hope that the models are as complete as possible. Yet the epidemiological models that have so transformed our world are seriously incomplete, and therefore fundamentally inadequate.

Any medical therapy is supposed to be tested for both efficacy and safety. There have been several studies19 examining the effectiveness of the lockdowns in combating the spread of the COVID-19 virus, with mixed conclusions.

So far, however, none of these studies or models have analyzed the safety side of the lockdown therapy. In response to questions from physician Sens. Rand Paul and Bill Cassidy, Dr. Anthony Fauci admits20 this side of the equation has not been accounted for in the models now driving our world.

As noted in an open letter21 recently signed by more than 600 health-care professionals, the public health costs from the lockdowns — described as a 'mass casualty incident' are real and growing.

These models are estimations based on existing research. The constantly changing projections of coronavirus deaths are extrapolations from research on previous epidemics. Yet modelers have no excuse for leaving evaluations of the lockdowns' massive costs to public health out of their models."

How does the "lockdown therapy" affect public safety? In his article, Lucas highlights the following:22
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• Increased chronic disease rates due to unemployment, poverty and putting non-COVID medical care on hold -- Research23 by the Veterans Administration has shown delaying cancer treatment for just one month led to a 20% increase in mortality. Another study24 found each one-month delay in breast cancer diagnosis increased mortality by 10%
  
• Increased rates of mental health problems due to unemployment and isolation
  
• Increased mortality rates from suicide -- In one study,25 being unemployed was associated with a twofold to threefold higher relative risk of suicide. A more recent study26 estimates "deaths of despair" linked to lockdowns may be around 75,000 in the U.S.
  
• Reduced collective life span -- Extended unemployment is also associated with shorter, unhealthier lives. Hannes Schwandt, a health economics researcher at Northwestern University, estimates an extended economic shutdown could shorten the lifespan of 6.4 million Americans entering the job market by an average of about two years.27 Lucas notes:

"If epidemiologists don't care to take account of this toll, another profession must. A study28 just released by a group of South African actuaries estimates that the net reduction in lifespan from increased unemployment and poverty due to a national lockdown will exceed the increased lifespan due to lives saved from COVID-19 by the lockdown by a factor of 30 to 1.

In other words, each year of additional life attributable to isolating potential coronavirus victims in the lockdown comes at a cost of 30 years lost due to the negative public health effects of a lockdown …"

Lack of education is also associated with significantly shorter life spans and poorer health. High school drop-outs die on average nine years sooner than college graduates,29 and school closings disproportionally affect poorer students.

As noted by Lucas, in addition to calculating the overall costs on society, modelers must also determine "on whom those costs fall," because the costs are not borne equally by all. The consequences of the lockdowns disproportionally affect those who are already the most vulnerable — financially and health wise — such as those living near the poverty line, the chronically ill, people with mental illness and minorities in general.
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"Contrary to the PR slogan, we are NOT all in this together," Lucas writes.30 "We need less insipid pro-lockdown propaganda extolling the virtues of the 'essential' workers, and more serious analysis of the enormous public health toll the lockdowns are imposing on them. Otherwise, we may come to see the era of coronavirus as simply the time where pro-lockdown elites sacrificed the working class31 to protect themselves."

An October 28, 2020, article featured by the Ron Paul Institute points out that:32

"Ever since the alleged pandemic erupted this past March the mainstream media has spewed a non-stop stream of misinformation that appears to be laser focused on generating maximum fear among the citizenry.

But the facts and the science simply don't support the grave picture painted of a deadly virus sweeping the land. Yes, we do have a pandemic, but it' a pandemic of ginned up pseudo-science masquerading as unbiased fact."

Nine facts that can be backed up with data "paints a very different picture from the fear and dread being relentlessly drummed into the brains of unsuspecting citizens," the article states. In addition to the fact that PCR testing is practically useless, for all the reasons already mentioned, these data-backed facts include:

1. A positive test is NOT a "case" — As explained by Dr. Lee Merritt in her August 2020 Doctors for Disaster Preparedness33 lecture, featured in "How Medical Technocracy Made the Plandemic Possible," media and public health officials appear to have purposefully conflated "cases" or positive tests with the actual illness.
   
   Medically speaking, a "case" refers to a sick person. It never ever referred to someone who had no symptoms of illness. Now all of a sudden, this well-established medical term, "case," has been completely and arbitrarily redefined to mean someone who tested positive for the presence of viral RNA. As noted by Merritt, "That is not epidemiology. That's fraud."
   
   
2. According to the CDC34 and other research data,35 the COVID-19 survival rate is over 99%, and the vast majority of deaths occur in those over 70, which is close to normal life expectancy.
   
   
3. CDC analysis reveals 85% of patients testing positive for COVID-19 wore face masks "often" or "always" in the two weeks preceding their positive test. As noted in the Ron Paul article,36 "The only rational conclusion from this study is that cloth face masks offer little if any protection from Covid-19 infection."
   
   
4. There are inexpensive, proven successful therapies for COVID-19 — Examples include various regimens involving hydroxychloroquine with zinc and antibiotics, quercetin-based protocols, the MATH+ protocol and nebulized hydrogen peroxide.
   
   
5. The death rate has not risen despite pandemic deaths -- Data37,38 show the overall all-cause mortality has remained steady during 2020 and doesn't veer from the norm. In other words, COVID-19 has not killed off more of the population than would have died in any given year anyway.
   
   

As noted in the Ron Paul article,39 "According to the CDC as of early May 2020 the total number of deaths in the US was 944,251 from January 1 — April 30th. This is actually slightly lower than the number of deaths during the same period in 2017 when 946,067 total deaths were reported."

All in all, there are many reasons to suspect that continued lockdowns, social distancing and mask mandates are completely unnecessary and will not significantly alter the course of this pandemic illness, or the final death count.

And, with regard to universal PCR testing where individuals are tested every two weeks or even more frequently, whether they have symptoms or not, this is clearly a pointless effort that yields useless data. It's just a tool to spread fear, which in turn allows for the rapid implementation of the totalitarian control mechanisms required to pull off The Great Reset. Fortunately, more and more people are now starting to see through this plot.

About 45,000 scientists and doctors worldwide have already signed the Great Barrington Declaration,40 which calls for the end to all lockdowns and implementation of a herd immunity approach to the pandemic, meaning governments should allow people who are not at significant risk of serious COVID-19 illness to go back to normal life, as the lockdown approach is having a devastating effect on public health — far worse than the virus itself.41,42 The declaration states:43

"Coming from both the left and right, and around the world, we have devoted our careers to protecting people. Current lockdown policies are producing devastating effects on short and long-term public health …

The most compassionate approach that balances the risks and benefits of reaching herd immunity, is to allow those who are at minimal risk of death to live their lives normally to build up immunity to coronavirus through natural infection, while better protecting those who are at highest risk. We call this focused protection."
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The declaration points out that current lockdown policies will result in excess mortality in the future, primarily among younger people and the working class. As of November 5, 2020, The Great Barrington Declaration44 had been signed by 11,791 medical and public health scientists, 33,903 medical practitioners and 617,685 "concerned citizens."45

As mask mandates on children sweep the nation, HighWire host Del Bigtree’s 11-year-old son, Ever, joins him on stage to test his levels of carbon dioxide inside a mask, face shield, and cloth bandana. The results from the OSHA approved testing device may likely shock any parent or person with a chronic lung disease such as asthma, chronic bronchitis, restrictive airway disease, COPD, lung cancer, etc.