Heavily armed police search Swiss doctor’s office after mask exemptions
Free West Media | June 12, 2022
Apparently the stance against doctors who work according to their Hippocratic oath and the medical code of ethics is being tightened internationally.
The enforcement of masks is an important goal in order to be able to continue the pandemic, as is known from internal protocols of the Israeli Ministry of Health or statements by the Austrian Director of Public Health. Masks have become a sign of submission while at the same time renouncing fundamental rights.
Even in Switzerland, which is known to be more liberal with the measures and had already lifted many random measures in mid-February, completely disproportionate action was taken against doctors. On social media, users likened the raid to how police would normally respond to a terror threat.
This is already happening in Germany, as the criminal judgment against Dr. Ronald Weikl showed. In Germany, such an act would be less surprising in view of the many house searches, even against judges who had issued “unwanted” judgements, also in connection with masks for children.
The regional court of Passau, Germany is expected to pass a verdict against the “mask doctor” Weikl for writing blank exemption certificates against the mask requirement.
“Whether it was a matter of issuing false health certificates, which is punishable under §278 of the German Criminal Code (StGB), as alleged by the prosecution, or only of medical certificates, for which §278 (StGB) does not apply at all,” noted the Children’s Health Defense Fund.
Weikl acted in the best interest of his patients, his lawyer explained and this should not have led to an indictment due to the lack of a criminal act on his part. The legal principle of nullum crimen, nulla poena sine lege applies, which means that one cannot be punished for doing something that is not prohibited by law – showing concern for his patients and especially children.
The law in Switzerland expressly provides for exceptions to the mask requirement. However, some authorities and the public prosecutor’s offices obviously do not care. For months there has been a veritable witch hunt against doctors who are critical of the measures.
Like Weikl, the Bern psychiatrist Dr. medical Ruke Wyler had issued mask certificates for her patients. The practice of the psychiatrist, who had only fulfilled her medical duty, was stormed in a heavy and a completely disproportionate police operation.
The scientific network Aletheia reported on the raid on the doctor’s practice. Critical doctors who question Corona measures to protect their own patients are being addressed and sanctioned, both abroad and in Switzerland.
Under the supervision of armed police officers wearing bulletproof vests, her computer hard drive was confiscated and patient files were taken away. People who wanted to support the doctor were asked to leave the building under threat of violence.
The Aletheia network said they were extremely concerned about these developments. Doctors who had issued mask certificates for the benefit of their patients did so because, after a thorough study of the data, they had come to the conclusion that wearing masks would be of no benefit, would be only harmful, first and foremost for children.
The medical certificates issued by the doctor could in no way be deemed to be incorrect since there has been no examination by the police or the public prosecutor’s office; this is a matter for medical expertise and the professional code of conduct for physicians. Medical professionals are free from directives, especially from non-physicians.
The vast majority of Corona measures are based on the narrative of the epidemiologically relevant asymptomatic transmission of SARS-CoV-2, which has long been refuted. This means that all non-pharmacological measures that go beyond hygiene and self-isolation for sick people (antisocial distancing, masks in public spaces, isolation, quarantine, contact tracing, school closures and curfews) are ineffective and harmful for asymptomatic people who were previously considered healthy.
Are We Entering the Next Phase of Our Medical Despotism?
By Rob Slane | The Blog Mire | June 10, 2022
One of the many things that continues to baffle me about the public response to all things Covid, is that the number of people demanding answers to the following questions is pitifully and inexplicably low:
- Who was behind the creation of SARS-CoV-2?
- Why were they making it?
- How and why did it get unleashed on the world?
These questions should unite both those who believe with their whole heart that Lockdowns were necessary and saved lives, and those like me who believe they were utterly futile on their own terms, and have caused untold destruction. They should unite both those who believe that masks were necessary and saved lives, and those like me who believe them to have been utterly futile on their own terms, and a destructive dehumanising force designed to perpetuate fear. They should unite both those who think that the so-called vaccines were safe and effective, and those who believe these blood-clotting, immune-suppressing, gene-editing injections to have been useless on their own terms, and the cause of mass casualties, which will one day be found to have killed millions upon millions of people over the course of several years.
All of us should be demanding who was behind this, why they were doing it, and how it came to be unleashed on humanity. For the fact is that a cytotoxic Spike Protein, with HIV Gp120 inserts which infect and destroy immune cells, was created in a laboratory and added to a coronavirus in gain-of-function research. Why are people not interested in who did this to them and why? Why are they not interested in who was behind something that was used to basically mess up their lives, and the entire planet, for the last two years, and long into the future.
If this were a movie, everybody would be waiting with baited breath for the super villains — Fauci, Daszak, Baric, Gates, Schwab to name but five — to face the reckoning. And yet crickets. It’s a bit like if Hitler had survived in 1945 and the Jews and other people groups who suffered under his murderous regime shrugged their shoulders and said, “We need to move on. When’s my next holiday coming?” To those who think the comparison is ludicrous, I would point out that the official number of deaths from the lab-created, souped up coronavirus now exceeds the number 6 million — an infamous historical number — and I would add to it that the number of deaths from Phase 2 of the operation will, in the end, dwarf that number many times over.
What do I mean Phase 2 of the operation? I mean the fiendishly clever plan to inject billions of people around the world with a totally new, experimental product which would cause their bodies to produce the same gain-of-function Spike Protein, replete with the HIV Gp120 insert, by the billions, for an unknown amount of time. The entire point of Phase 1 — the release of the lab-created SARS-CoV-2 — was to create the fear that would lead to these injections. Does anybody seriously still believe these products were an improvised, off-the-cuff response to that virus? If so, perhaps they’d care to explain how all four major manufacturers of these products (Pfizer, AstraZeneca, Moderna, Johnson and Johnson) all just happened to choose the same cytotoxic Spike Protein as the part of the virus that the human body would produce? As Mike Yeadon, former Pfizer VP for Allergy and Respiratory Research has pointed out, it is the most dangerous part of the virus, as well as that which mutates the most quickly, making it the most unsuitable part to use in a vaccine. And yet four companies did just that. Perhaps they’d also care to explain Moderna’s confidentiality agreement with the National Institute of Allergy and Infectious Diseases (NIAID) to ‘transfer mRNA coronavirus vaccine candidates’ in December 2019. There is no doubt at all that Covid-19 was known about long before you and I ever got to hear about it, as this mention of it in the US Department of Defense database in November 2019, in a contract connected to one of those harmless and benevolent Ukrainian biolabs, clearly shows. There is, therefore, no doubt that the manufacturers of the bioweapon masquerading as a vaccine knew about it and were on it well before it was a thing for the rest of us.
These so-called vaccines, which were never safe nor effective, have already killed or maimed millions around the world. But the real damage is only just beginning. Not only do they train the body to produce antibodies to fight a non-existent enemy — the long-departed original SARS-CoV-2 Spike Protein, which is a bit like the 21st Century British Army training to fight a battalion in Hitler’s Wehrmacht — but even more crucially, they infect and kill crucial T-cells. Which is why the ‘vaccinated’ keep getting Covid reinfections — their immune systems have been left defenseless, and with each recurring bout it becomes increasingly depleted.
Which brings us on to Phase 3. Whilst Phase 1 was about freaking people out with a virus that was dangerous to very few (albeit eminently treatable), and Phase 2 was about injecting people with the poison shot masquerading as the solution, Phase 3 is — I believe — all about covering up the effects of the depleted immune systems of millions of people, to ensure that most people continue to ask no questions and many of them ‘go gentle into that good night’. How? By the release of another lab-created, gain-of-function pathogen, which will be used to explain away the ‘mysterious’ deaths of people with crippled immune systems. If Phase 1 and 2 were fiendishly clever, this is from the pit of Gehenna itself.
Alarmingly, there is a probability that such a pathogen has indeed been released, although it is still too early to know if this is what a grinning William Gates III described as ‘the next one’. Much like the Event 201 simulation in October 2019, which just happened to simulate a global coronavirus pandemic, at the March 2021 Munich Security Conference a ‘Tabletop Exercise’ was conducted entitled, ‘Strengthening Global Systems to Prevent and Respond to High-Consequence Biological Threats.’ Here’s the blurb:
“The exercise scenario portrayed a deadly, global pandemic involving an unusual strain of monkeypox virus that emerged in the fictional nation of Brinia and spread globally over 18 months. Ultimately, the exercise scenario revealed that the initial outbreak was caused by a terrorist attack using a pathogen engineered in a laboratory with inadequate biosafety and biosecurity provisions and weak oversight. By the end of the exercise, the fictional pandemic resulted in more than three billion cases and 270 million fatalities worldwide.”
Hmm? A Monkeypox pandemic! Starting when exactly? Why, would you believe it — in mid-May 2022. And lo and behold, in mid-May 2022, an outbreak of an unusual strain of Monkeypox began. As per the timeline set out on page 10 of their document, the international response would then start around 5th June 2022. And would you believe it, in this last week which began on 5th June, the Center for Disease Control (CDC) update its alert level for Monkeypox to Level 2, the UK Government upgraded Monkeypox to the same category of diseases as leprosy and plague, and the WHO came along to claim that the virus may be spread by ‘community transmission’. Add to this that this particular strain of Monkeypox appears to have been lab-created, and almost inexplicably appeared in about 10 western countries at the same time, and it looks like the timeline in the simulation might not have been entirely a coincidence.
I’m genuinely unsure at this point whether Monkeypox is Phase 3. I’ve heard many say that it would be impossible to create the same level of fear as with Covid, but I’m not so sure. The 2021 Tabletop Exercise had 270 million deaths by the end of 2023, and I have this horrible feeling that a new lab-created pathogen, unleashed on a world where millions have just had their immune systems horribly damaged, could send many to untimely deaths. I pray not; I fear so.
But whether the next thing is Monkeypox, or the great Bird Flu pandemic, as predicted by former CDC Director Robert Redfield, or perhaps Covid redivivus, it is quite clear to anyone with their eyes open and their wits about them that we are well and truly enslaved in the Medical Despotism I predicted back in April 2020:
‘Being “led by the science” is turning out to be an unmitigated disaster, yet it will be “the science” — or Government-approved science — which will be proposed as the saviour. To stop such situations occurring again, we will be told that we must avail ourselves of more technology, more monitoring, more checks, more vaccines, more controls. … Personally, I’d rather trust myself into the hands of the Living God than surrender to the Bill Gatesian Social Distancing Medical Despotism of compulsory vaccines, certifications and health apps that is starting to take shape around us.’
I wish people had listened to the few of us who pleaded with them back then not to fall for the lies of the criminals who were foisting this upon us. Perhaps we could have halted it in its tracks.
Lockdowns: the evidence revisited
Professor Marilyn James, Professor of Health Economics, Professor David Paton, Professor of Industrial Economics | Health Advisory & Recovery Team | June 10, 2022
“It is possible that lockdown will go down as one of the greatest peacetime policy failures in modern history” – Professor Douglas Allen[1]
In March 2021, we wrote two sections in ‘Covid-19 the evidence’, namely ‘Economic impacts – the true cost of lockdown’ and ‘Lockdowns – do they work?’. Over a year later, we have revisited not only the financial costs of lockdowns but also the societal costs, the impact on healthcare and the lack of evidence for overall benefit.
Assessing the economic costs of lockdowns and other Covid-19 restrictions is not easy, partly because the pandemic itself would have impacted economic activity independent of Government restrictions. However, we do now have considerable evidence that both voluntary behaviour change and government restrictions have significant economic effects.[2],[3] Further, voluntary changes tend to have most impact on the activity of groups most vulnerable to Covid, whilst Government restrictions have a disproportionate effect on those least vulnerable. This means that not only do most mandatory restrictions have a significant economic impact, but any benefits in terms of reductions in hospitalisations or deaths are minimal.[4]
Many of the immediate economic consequences of lockdowns were masked by the eye-watering amount of money spent by governments on furlough and business support schemes. Given the limited evidence that stay-at home measures and business closures have any significant impact on infection rates[5], the question needs to be asked whether the billions spent paying business to shut down and people not to work could have been used better by building up capacity in the health system. The stay at home message of “protect the NHS” may have been no more than elaborate code for don’t highlight years of dwindling funding that failed to keep pace with growing population and demand in health care, with the NHS entering the pandemic with spending per GDP at the lowest level since 2009.[6]
Although furlough and business support schemes have had success in limiting the impact on unemployment, the longer-term economic consequences of lockdowns are now becoming clear. The lack of spending opportunities during lockdown contributes to a build-up of personal and corporate savings. As restrictions have eased, people begin to spend these savings and, combined with the supply chain issues that have built up in the meantime, sustained inflation is the inevitable result. Even worse, having spent about £70 billion[7] paying healthy people not to work via the furlough scheme and some £150 billion in total on support measures[8], the ability of the government to respond to this lockdown-induced cost-of-living crisis via either tax cuts or increased benefits, is limited due to the hit to public finances caused by lockdown-induced government spending.
It is perhaps no surprise that a series of research papers looking at data from Australia[9], the UK[10], Canada[11] and the US[12], have concluded that the costs of lockdowns exceed any plausible estimate of the benefits many times over.
The pandemic saw one disease prioritised over all others. It is now painfully clear that the “all others” are set to suffer with longer and larger health consequences than those of the covid-19 crisis itself. The report issued by the BMA is terrifying in every sense.[13] At the start of the pandemic 4.24m were waiting for elective treatment this now stands at 6.18m. Ridsdale makes the point “stay home” may well have contributed to excess deaths as people died at home without access to care and government policy prioritised covid above all other health concerns[14]. This figure of 6.18m masks and continues to mask the lack of referrals that occurred. There is no reason to suppose demand has dropped for elective care, yet, since the pandemic there have been 4.51 m fewer elective referrals. The latest figures show some 300,000 are waiting over a year for treatment. Again, this figure is masked by GPs under referring, reporting their ability to make referrals is severely constrained, yet the patients are still sitting at primary care level needing care. If the elective surgical figure continues to remain well below pre pandemic levels, NHS waiting lists will only continue to rise. Add to this routinely soaring long waits of over 12 hours at emergency department level and the gap between target time for cancer surgery and actual time to getting surgery increasing, the health picture created by covid prioritisation in the UK is frightening.
Lockdowns created isolation from our social and working worlds. The latest report from MIND states “Isolation and loneliness have made people’s mental health worse – with young people particularly badly affected.”[15] Similar can be said for older people especially those in care homes. The unintended consequences of removing activity, family and social interaction from the elderly may be more serious than the direct disease consequences of covid, with isolation being listed as cause of death in a number of care homes in the USA.[16]
Given what we now know, it is hard to disagree with the conclusion of Professor Doug Allen’s analysis of lockdown costs and benefits in Canada that “lockdown will go down as one of the greatest peacetime policy failures in modern history.” 1
References
- https://doi.org/10.1080/13571516.2021.1976051
- www.sciencedirect.com/science/article/pii/S0047272720301754?dgcid=rss_sd_all
- https://direct.mit.edu/rest/article-abstract/doi/10.1162/rest_a_01108/107399/Do-Stay-at-Home-Orders-Cause-People-to-Stay-at
- https://link.springer.com/article/10.1007/s42973-021-00077-9
- https://onlinelibrary.wiley.com/doi/10.1111/eci.13484
- https://www.health.org.uk/news-and-comment/charts-and-infographics/health-spending-as-a-share-of-gdp-remains-at-lowest-level-in
- Coronavirus Job Retention Scheme: statistics – House of Commons Library (parliament.uk)
- https://commonslibrary.parliament.uk/research-briefings/cbp-9309/#:~:text=Current%20estimates%20of%20the%20cost,per%20person%20in%20the%20UK
- https://link.springer.com/content/pdf/10.1007/s40592-021-00148-y.pdf
- https://www.cambridge.org/core/journals/national-institute-economic-review/volume/87652BB968C8244B2E478DAA353C7DF9
- https://doi.org/10.1080/13571516.2021.1976051
- https://sites.krieger.jhu.edu/iae/files/2022/01/A-Literature-Review-and-Meta-Analysis-of-the-Effects-of-Lockdowns-on-COVID-19-Mortality.pdf
- https://www.bma.org.uk/advice-and-support/nhs-delivery-and-workforce/pressures/nhs-backlog-data-analysis
- http://dx.doi.org/10.1136/bmj.m3515
- https://www.mind.org.uk/media/8962/the-consequences-of-coronavirus-for-mental-health-final-report.pdf
- https://www.nbcnews.com/news/us-news/hidden-covid-19-health-crisis-elderly-people-are-dying-isolation-n1244853
Weird that the “I-Believe-The-Science(TM)” crowd has completely given up on science
The NY Times announces that henceforth, clinical trials for Covid-19 shots must be abandoned because real world data makes the cartel look bad
By Toby Rogers | June 9, 2022
I. Pharma is losing the game so they are throwing the chess board across the room
The NY Times published a vile piece of fascist Pharma propaganda today. Berenson flagged the online version of the article yesterday. As you know, I have been yelling about the FDA’s Orwellian “Future Framework” for weeks because it’s literally the worst idea in the history of public health.
It turns out that it’s even worse than I thought.
Pharma has already begun a PR offensive to get it across the line and Sharon LaFraniere of the NY Times was eager to do their bidding.
Here’s what’s happening. The mRNA shots are not working against SARS-CoV-2. Everyone knows this. So Moderna and Pfizer are racing to reformulate these shots. The reformulated shots are not working either. Just last week Moderna was touting a bivalent shot that combined Alpha + Beta, but now, apparently, they’ve abandoned that approach. The NY Times article hypes a Moderna shot targeting earlier Omicron variants (it does not say, but perhaps BA.2 and BA.2.12.1?). However evidence from South Africa shows that BA.4 and BA.5 are outcompeting the earlier Omicron variants and the reformulated Moderna shot probably won’t work against the new strains (the virus evolved for a reason — to evade vaccines).
So what are predatory pharmaceutical companies and their feckless government enablers supposed to do!? Abandon clinical trials altogether!
Here’s how the NY Times describes this scheme:
… many experts worry that the virus is evolving so quickly that it is outpacing the ability to modify vaccines, at least as long as the United States relies on human clinical trials for results.
See, it’s not that coronavirus vaccine have failed over and over again (even though they have). It’s that This Wily Virus(TM) is just evolving so quickly that we could not possibly allow human clinical trials of coronavirus vaccines ever again. The only way to beat This Wily Virus(TM) at this point is to abandon science.
Of course it gets worse. The NY Times elaborates:
The problem is that Moderna and Pfizer — the maker of the other main coronavirus vaccine in the United States — do not have enough time now to run more human clinical trials and still manufacture shots before the fall, when the Biden administration is hoping to be able to offer an updated vaccine to counter what public health experts predict will be a winter surge.
See, it’s not that rapacious pharmaceutical companies want to suck all wealth out of the world and put it into their own pockets while setting up a 1,000 year Pharma Reich. No, no, no, silly. It’s just that they “do not have enough time” to do actual science anymore so they are just going to skip all that. Don’t you worry your little head about it.
Furthermore, only a conspiracy theorist would believe that the FDA has abandoned all of its statutory responsibilities to protect public health in order to prostitute themselves to Pharma. The Correct Understanding(TM) is that the FDA is being forced by circumstances outside their control to abandon science. This is not a problem because the cartel is truth, the cartel has always been truth, and since the cartel has decided to abandon science altogether then that’s the new science.
Henceforth, quite literally, the peasants will be forced every six months to inject whatever they are told, with no questions asked, and “they will be [required by law to be] happy about it”.
Instead of human clinical trials the FDA will rely on a few test tube and mouse studies. In the article, Fauci describes this as, “alternative pathways of decision.” That guy just oozes totalitarianism at this point.
So if the “Future Framework” is approved on June 28 the new rules will be: a pharmaceutical company can claim that some new injection creates antibodies in a test tube or mouse (that no one else can see or audit). Done! Ship it and inject it! That’s it. Even though the FDA admits that there are no “correlates of protection.”
In the replies to my earlier articles about the Future Framework some astute readers have pointed out that the FDA has already abandoned human trials when it comes to Covid-19 shots in kids. None of the Moderna or Pfizer clinical trials in kids showed any real world health benefit at all. So they switched to looking at antibodies in the blood and use this tortured mental gymnastics called “immunobridging” to conjure up hypothetical future benefits that never materialize in the real world. Abandoning even the pretense of human trials and moving to test tubes and mice is the obvious next step in this complete abandonment of science.
When people say “I Believe The Science(TM)” what they really mean is “I Support The Genocide.” That’s what’s happening. The FDA has not done science in two years, probably much longer than that.
There is no left and right in politics anymore. Just, the FDA Pharma Fascist Party where members are expected to participate in self-genocide for “the good of society” (read: the profits of the cartel)
vs.
the Rebel Alliance where we practice actual science, critical thinking, logic, and reason, and work every day to protect human health and dignity.
Any politician who wants the 18 million votes of single-issue medical freedom voters in November needs to know that there must be hearings, arrests, and trials of the bureaucrats at FDA, CDC, NIAID, HHS, and NIH who did this to us.
II. What is to be done?
In the meantime, here are the email addresses for all of the public health political appointees, FDA staff, and VRBPAC members who have a say in connection with the “Future Framework”. Please contact them to urge them to reject this nonsense (proposed subject line and email text below — or share your own personal story).
Subject line: The “Future Framework” is the WORST idea in the history of public health. Please vote NO.
1. No Covid-19 shots for kids that failed clinical trials. According to the journal Nature Medicine, children and young people have a 99.995% recovery rate. According to the CDC, the overwhelming majority of children already have natural immunity. The harms from Covid-19 shots in kids are catastrophic.
2. The FDA and CDC must pivot to therapeutics. About twenty off-the-shelf treatments are more effective than vaccines (if used for prophylaxis or early intervention). Get these safe and effective medicines to people who need them and let doctors be doctors again and treat patients based on their own best clinical judgment.
3. Any reformulated Covid-19 shots MUST go through proper HUMAN clinical trials and FDA review. That means:
• large (50,000+ person) double-blind randomized controlled trials with inert saline placebos conducted by an independent third party;
• safety and efficacy studies for two years prior to any application; monitor the treatment and control group for the rest of their lives to record non-specific effects;
• must provide sterilizing immunity with greater than 90% efficacy and less than 0.1% Grade 3 Adverse Events; and
• proper monitoring for carcinogenesis, mutagenesis, and impairment of fertility.
[Contact list:]
sean.mccluskie@hhs.gov, commissioner@fda.hhs.gov, DeanofPublicHealth@brown.edu, Aux7@cdc.gov, Peter.Marks@fda.hhs.gov, Hong.Yang@fda.hhs.gov, Richard.Forshee@fda.hhs.gov, Huilee.Wong@fda.hhs.gov, Leslie.Ball@fda.hhs.gov, Doran.Fink@fda.hhs.gov, CBERVRBPAC@fda.hhs.gov, hanae@bcm.edu, paula.annunziato@merck.com, adam.berger@nih.gov, hbernstein@northwell.edu, acohn@cdc.gov, anc0@cdc.gov, hjanes@fredhutch.org, hgans@stanford.edu, david.kim@hhs.gov, asmonto@umich.edu, offit@chop.edu, spergam@fredhutch.org, Jportnoy@cmh.edu, erubin@hsph.harvard.edu, erubin@nejm.org, ashane@emory.edu, swamy002@mc.duke.edu, fullerao@umich.edu, bgellin@rockfound.org, RandyHawkins@cdrewu.edu, officeofthepresident@mmc.edu, JYLee@uams.edu, ofer.levy@childrens.harvard.edu, wayne_marasco@dfci.harvard.edu, cmeissner@tuftsmedicalcenter.org, mrn8d@virginia.edu, stanley-perlman@uiowa.edu, reingold@berkeley.edu, mhsawyer@ucsd.edu, mew2@cdc.gov
III. The FDA has opened the formal comment portal for the “Future Framework”
If you prefer the official route, you can lodge a formal comment with the FDA by following the instructions (here). Enter docket number FDA-2022-N-0905 at https://www.regulations.gov by June 22 to tell the FDA what you think of their proposed plan to abandon clinical trials for Covid-19 shots in perpetuity.
THE WHO, PANDEMIC PREPAREDNESS, AND THE IMPORTANCE OF FALSE MESSAGING
By Dr David Bell | Pandemics – Data and Analytics | June 9, 2022
The World Health Organization (WHO), and the growing pandemic preparedness industry sponsoring it, has faced considerable challenges in maintaining support for its COVID-19 response. It has addressed this difficult situation with simple and uniform messaging. The compliance thus achieved by the WHO has been vital to achieving a successful concentration of wealth, benefitting not just its major sponsors, but also the army of global health staff who have remained obedient throughout.
Threatening this progress, a skeptical minority within the public sphere have been using evidence and rational argument to undermine the pandemic industry’s potential. As the pandemic preparedness and response narrative is poorly defensible on rational criteria, such criticism and opposition must be dealt with and dismissed by other means. This is being achieved through the creation of a dogma around mass COVID-19 vaccination sufficiently separated from reality as to render the normal processes of debate irrelevant. If the gap between pandemic messaging and reality can be kept sufficiently wide, few passengers can step off, and this lucrative gravy train becomes unstoppable.
Small lies can be argued against, big lies become matters of faith
The development and mass deployment of vaccines has been a key component of the COVID-19 response, underpinning much of the transfer of wealth from lower-income people and countries to large Pharma, their investors and the global health workforce they sponsor. Against a background of rapidly increasing global poverty, this unprecedented increase in wealth has in turn raised the potential for unprecedented funding to global health institutions – the mostly Western-based industry that fills offices and drains aid budgets in Europe and North America. A significant cognitive decoupling has been necessary across this sector to achieve sufficient uniformity of voice and purpose, as the institutions involved were ostensibly intended to improve the health and uphold the rights of those less financially fortunate. To achieve success, staff of the WHO and other international organizations therefore had to be enabled to signal virtuous intent while acting in concert for corporate gain.
Vaccines traditionally protect the vaccinated against a target pathogen and humans tend to develop good immunity after respiratory virus infections. These two realities create an urgent problem for the pandemic preparedness industry, as the increased financing set to expand their reach is dependent on successfully convincing the world that these truths are indeed fallacies. Thus, to sell COVAX, the WHO’s financing facility for mass COVID-19 vaccination and the model for future pandemic responses, it was vital for the WHO to ensure that the obvious nonsensical nature of the programme would be ignored. This required coordination and adherence to a single simple message, repeated incessantly to stifle external opinion; a slogan so ridiculous that it becomes inarguable. In other words, it required propaganda.
It is essential to focus people on simplistic slogans if the aim is to suppress their tendency for independent thought and to make any venture in that direction a cause of stress. If people can see their respected authority figures standing behind a statement that is otherwise obviously false, it becomes easier to accept that the false must be true than to stand alone against authority and the crowd. Once one’s colleagues are on-board, the Asch conformity phenomenon kicks in – if everyone else is saying ‘X’, then it surely must be ‘X’, even if it looks like ‘Y’. If a health programme flies in the face of all existing medical knowledge, it must therefore be supported by a sufficiently strong dogma to negate evidence-based arguments. It is a testament to the power of group-think, loyalty to sponsors and the allure of money that this has, thus far, been brilliantly achieved.
COVAX – Selling the golden goose
“No one is safe, until everyone is safe”, the WHO’s COVAX motto, fulfills all the above criteria.
Most people want to be safe – and to achieve industry aims, the public must be convinced that others, not just themselves, are the key to their personal safety. They must support the blame or coercion being applied to these others. But the brilliance of ‘No one is safe, until everyone is safe’ is not just in its appeal to self-preservation and its divisiveness, but in its simple stupidity.
1) For the slogan to be true, the vaccine must be transmission-blocking only. It must not protect the vaccinated individual. Otherwise, their safety will not be dependent on the vaccination of others. However, the WHO and its partners also claim that “COVID-19 vaccines provide strong protection against serious illness, hospitalization and death”. Therefore, in promoting its ‘No one is safe’ slogan, WHO staff must collectively proclaim a falsehood. This builds loyalty and cohesion, as a lie is more easily maintained within a like-minded group.
2) To be ‘safe’ from a virus, one must either be intrinsically at very low risk (as most people are to most viruses) or gain immunity.
- ‘Intrinsic low risk’ created a huge problem for the mass-vaccination narrative early in the COVID-19 outbreak, as data from China showed the very strong skew of severe COVID-19 towards old age, and association with certain comorbidities. Most people are clearly at minimal risk. This had to be suppressed to enable mass-vaccination – all must consider themselves at risk. Public health agencies and their corporate backers even proclaimed impending catastrophe for the people of sub-Saharan Africa, more than half of whom are under 20 years of age. The use of age-based disease metrics, standard for disease-burden assessments up to 2019, were put aside and ‘COVID-19’ mortality reported as raw mortality numbers only.
- Immunity presents a problem, as it is both the pathway through which vaccines work, and the way we naturally gain protection. Immunity makes us safe, but natural immunity is useless to investors. While a safe vaccine would be preferable to a dangerous virus, once infection has occurred the gain from vaccination is minimal. This poses an immediate threat to profits and share price. The response to this dilemma included one of history’s more ludicrous statements from a global institution, when the WHO modified its herd immunity definition to only recognize immunity resulting from pharmaceutical intervention. This is nonsense to anyone with even a rudimentary understanding of immunology, and of course the WHO’s staff have at least rudimentary knowledge.
Inevitably, SARS-CoV-2 has continued spreading, including from the vaccinated. Based on serology from Africa, India and the USA, and the highly transmissible Omicron variant, we can now be confident that nearly all the world’s population have post-infection immunity. It is no biological surprise that immunity gained from a respiratory tract infection with whole virus reduces disease severity more effectively than injection with spike-protein or its mRNA precursors. Claiming that mass vaccination still has public health relevance in these populations requires both abandonment of logic, and a willingness to dispense with decades of prior scientific learning. It requires acceptance of dogma.
A final component of the COVAX strategy, to lock-in celebrity support and enable those promoting the vaccine to still feel virtuous, is ‘vaccine equity’. People in rich countries are having boosters whilst many of the ‘global poor’ still await their first doses. The lack of benefit to be obtained from these doses, and the requirement of coercion to attain high coverage, are irrelevant – inequity in vaccine distribution simply has to be ‘bad’. Whilst pushing more boosters on high income markets, the same Pharma companies can look good by demanding vaccine equity, advocating for the ‘disadvantaged’. In reality this diverts resources from areas of greater need, thereby killing more children, but such fine print will never make the front pages. Commodity equity expands markets and provides returns, while health equity does not. Fear of being vilified as anti-equity helps keep skeptics quiet.
Bolting down the golden goose
Science, including public health, were previously held to be based on processes of logic, based on an acceptance that aspects of our world are grounded in discoverable truth. This concept is a threat to COVAX and the wider pandemic preparedness narrative. It is a threat to the return on investment of the pandemic industry’s sponsors. Greed is a stronger driver than truth, and it must be allowed to run free if society is to be truly reset in favor of those who wish to concentrate and control its wealth.
Despite its massive internal contradictions, disproportionate cost, coercion, and requirement for its promoters to live obvious lies, COVAX and the entire mass-vaccination paradigm has created a strong model for the success of the wider pandemic preparedness project. If truth in public health can be so readily dispensed with, and those working in the field so willingly corralled, the potential for milking the public’s trust and desire for safety presents unprecedented potential for profit. As this wealth accumulates, it supports the continuing advocacy and manipulation required to keep its adherents loyal. This creates a self-perpetuating cycle – we can expect to see more outbreaks, health emergencies and pandemics declared, more vaccines rolled out, and more wealth concentrated as a result. An unstoppable cycle burying truth under a growing fog of fear and falsehood.
That, at least, is the plan. The eventual outcome will depend on whether truth, human rights, equality and trust were ever fundamental to maintaining societal cohesion and peace. If they were, then let us hope the chaos that follows their abandonment is somehow contained. For now, business is business, and the golden goose, bolted down in a hall of lies, will keep on laying.
Where’s the Emergency? 18 Congress Members Demand Answers as FDA Set to Approve COVID Shots for Kids Under 5
The Defender | June 8, 2022
Members of Congress today demanded answers from Dr. Robert M. Califf, commissioner of the U.S. Food and Drug Administration (FDA), as the agency reviews Emergency Use Authorization (EUA) for COVID-19 shots in children age 5 and under.
The FDA’s Vaccines and Related Biological Products Advisory Committee (VRBPAC) is meeting on four separate occasions in June to discuss additional EUAs that would provide cradle-to-grave COVID-19 shots — and to consider a “Future Framework” that will permanently lower the bar for safety and efficacy, according to Toby Rogers, Ph.D.
A letter signed by Sen. Ted Cruz (R-Texas), Rep. Bill Posey (R-Fla.) and 16 other members of Congress today asked Commissioner Califf 19 questions about the safety of COVID-19 vaccines for young children.
The questions focused on the youngest children (6 months to 5 years) due to the Congress members’ concerns about what they called the FDA’s “one-size-fits-all” approach to the vaccines.
“The data show that the risks of serious adverse outcomes for COVID for children five and under is very low and as such the standard for evaluating EUA interventions must be very high,” the letter states.
“We believe it is prudent and necessary that the FDA provide answers to a number of questions before approving EUA vaccines for children under age 5, including more than 70% of whom are already seropositive for COVID-19.”
The VRBPAC meetings began Tuesday. The meeting schedule is:
- June 7 — EUA for Novavax’s COVID-19 shot for adults.
- June 14 — Amendment to Moderna’s EUA to include primary series to children and adolescents 6 through 17 years of age.
- June 15 — Amendment to Moderna’s EUA to include primary series for children 6 months to 5 years and amendment to Pfizer’s EUA to include the primary series to children 6 months through 4 years of age.
- June 28 — Proposed “Future Framework” for COVID-19 shots.
The Congress members’ letter presses the FDA to address unanswered questions regarding the risks and benefits of administering COVID-19 vaccines to children.
They ask the FDA to explain, among many other things:
- What the cardiac risk factor is for children who receive EUA COVID-19 vaccines.
- Why the FDA recently lowered the efficacy bar for COVID-19 vaccines for the youngest children.
- When the FDA and the Centers for Disease Control and Prevention (CDC) will provide the public with more details on children’s serious adverse outcomes from COVID-19 infections.
- If it is possible that administering the vaccines in young children could predispose them to increased risk from future novel COVID-19 variants.
- How many children ages 5 and under with and without pre-existing medical conditions have died from COVID-19 or its variants.
Finally, the letter asks Commissioner Califf to “please list the medical emergencies [among] children 0 to 4 years old that enables the FDA to approve the COVID vaccine for children using its EUA.”
Children’s Health Defense calls for action
Mary Holland, Children’s Health Defense (CHD) president and general counsel, called the FDA’s Future Framework proposal “quite possibly the worst idea in the history of public health.”
Children under 18 with no comorbidities have virtually no risk of death from COVID-19, according to a November 2021 study published in Nature.
A July 2021 preprint paper found children have a 99.995% recovery rate, and the vast majority of children have minimal symptoms.
The Nature study described how children between 3 and 11 years of age mount effective, robust and sustained immune responses to COVID-19.
The CDC’s own data show that at least 75.2% of children ages 0 to 11 and 74.2% of adolescents ages 12 to 17 already have superior natural immunity.
There is no clinically significant health benefit from the mRNA vaccines, according to Moderna. Reporting on its Phase 2/3 KidCOVE study, the company said, “the absence of any severe disease, hospitalization or death in the study precludes the assessment of vaccine efficacy against these endpoints.”
Preliminary data showed the shots were only about 44% effective at preventing symptomatic infection in children 6 months to 2 years old, and 37% effective in children ages 2 to 5 — both below the 50% level that regulators generally called the minimum level for EUA approval in 2020.
In New York, officials observed that Pfizer’s efficacy against Omicron plummeted from 68% to 12% after 7 weeks in children ages 5 to 11.
“These shots are dangerous and carry very real risks,” Holland said.
Studies show vaccinated children face a substantial risk of myocarditis. Moderna’s EUA application, originally filed in June 2021, has already been held up because of a clear safety signal for myocarditis, which prompted a number of European countries to prohibit its use in young people.
Additionally, the Vaccine Adverse Events Reporting System or VAERS has more than 48,500 reports of adverse events in children, including 112 deaths (as of May 27), and a growing number of reports of encephalopathies, clotting issues, diabetes and neurological problems in children following COVID-19 shots.
© 2022 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.
Shanghai lockdowns increase market for invasive medical surveillance tech
By Will Henney | Reclaim The Net | June 10, 2022
The South China Morning Post interviewed experts who believe there could now be a big market for facial recognition cameras to “detect signs of COVID-19.”
The news outlet cited a report by Everbright Securities that claimed that about 2 million devices for detecting infection and confirming vaccination and test results could be put in public venues like entertainment venues, hospitals, office buildings and shopping centers.
Everbright estimated that the market to be about 50 billion yuan ($7.5), with market leaders like Hikvision and SenseTime expected to leverage the opportunities. Another player in the surveillance market, Telpo, already makes facial recognition technology that can check the temperatures of multiple people.
The paper quoted Wang Feng, a financial services expert, saying: “The market potential here cannot be matched anywhere else in the world, because these smart devices will be widely used in big cities to meet stringent virus control rules. Operators of shopping malls and cinemas will buy the machines to improve efficiency of their verification processes.”
The facial biometrics device would, in theory, check test results, vaccination status, and recent movements before allowing someone to enter a certain venue. Everbright said that each device would cost between 2,000 and 10,000 yuan ($300 to $1,500).
Covid Passes – and coercion – are here to stay
By Niall McCrae | TCW Defending Freedom | June 10, 2022
So the Covid Pass was not just for Christmas. Despite all the rhetoric of ‘living with Covid’, the Civil Service seeks two deputy directors for further development of this digital health certification (one a ‘delivery lead’, the other a ‘service management’ role). Seemingly a coronavirus outbreak is being exploited to usher in technocratic surveillance whereby the state will know our every movement. And given the excuse of another pandemic, or perhaps a climate-related emergency, such movement will be readily curtailed.
Looking back, we can see how society was primed by the authorities and mainstream media for the language of a ‘new normal’. The term ‘lockdown’, first used in a US prison setting, began to appear in British newspapers several years ago, typically in hyperbolic Daily Express reports of an incident in a railway station or department store. Was this predictive priming? Soon after Covid-19 emerged, the media were warning of ‘Long Covid’. As we now know, mRNA vaccines were already patented, and perhaps this syndrome was a prepared disguise for the likely litany of vaccine injuries; every symptom under the sun was included.
‘Long Covid’, though, may have a different and darker meaning. The Covid-19 regime has set a precedent, and draconian infection controls could be reinstated at any time. Anyone who thinks Covid-19 is over is very naïve. In places as diverse as Portugal, Finland, North Korea and New York the disease has returned to the headlines, with summer surges feared owing to holidaying, festivals and other socialising (otherwise known as fun). The virus will never officially disappear, and a largely compliant public will accept public health controls while dissidents will be forced to comply or suffer the consequences.
Vaccine passports, like Covid, are ready to pounce again. They were introduced in a limited way in England, while the devolved administrations of Scotland, Wales and Northern Ireland went much further. Nicola Sturgeon, a leader who basked in the glow of ‘saving Scots’ lives’, imposed restrictions long before and after the allegedly reckless rulers in Westminster.
It was as recently as January this year that the Scottish government expanded the use of vaccine passports. Adults needed to show proof of being fully vaccinated (less than four months since last jab) or a negative test before admission to nightclubs, unseated indoor events with more than 500 people, unseated outdoor events with over 4,000, and any event with more than 10,000 in attendance.
Many commentators believed that the SNP was using Covid-19 as a wedge in its independence drive, but the Labour assembly in Wales was just as extreme. In January Big Brother Watch launched a judicial review against Welsh ministers for its vaccine passport regime. Lawyer Shirin Marker of Bindmans LLP said: ‘In maintaining the Covid Pass Scheme, the Welsh government is exercising an unprecedented level of control over the rights and freedoms of the public. In these circumstances, it is essential that the Welsh government is transparent about what evidence they have relied upon to impose the scheme. Unfortunately, to date, such evidence has not been forthcoming.’
I suspect that decisions were made at UK level to use the Celtic fringes to test the water. Whereas the Scots and Welsh were manipulated by national consciousness, the awkward English have too many Samuel Bamfords against the establishment. And another Peterloo could turn the tide. Remember the poll tax riots, after the policy was introduced in Scotland with little resistance.
While he was still fooling us with Churchillian rhetoric, Boris Johnson repeatedly expressed his opposition to identity cards, an authoritarian creep of Tony Blair’s government. In the Daily Telegraph in 2004 he wrote: ‘There is the loss of liberty, and the creepy reality that the state will use these cards – doubtless with the best possible intentions – to store all manner of detail about us, our habits, what benefits we may claim, and so on.’
Yet as Prime Minister throughout the Covid-19 debacle, Johnson has keenly promoted the ‘build back better’ agenda espoused by the World Economic Forum. He agrees with WEF leader Klaus Schwab that we cannot return to the ‘old’ normal. While the British people feel they have left Covid-19 behind, at least for now, Johnson’s administration is spending public money to advance the Covid Pass. He will know of plans on a global scale, about which we can merely speculate. The enthusiasm of ministers for a new pandemic treaty, which would override national democracy, shows that we remain in the ratchet. What was Michael Gove doing at the recent Bilderberg meeting in Washington?
The blurb in the job advertisement states that the Department of Health and Social Care, which is administering the Covid Pass, is ‘central to the government’s response to Covid-19, the biggest challenge the country has faced in a lifetime’. Really? If there had been no constant barrage of sensational media messages in the last two years we would have carried on our lives regardless. Many of us know more victims of vaccine injury than of the virus itself.
Referring to the Prime Minister’s ‘Living with Covid’ strategy, the advert notes that ‘the NHS Covid Pass will be required at events and for international travel for the foreseeable future’. Living with Covid means never letting Covid go. And it is obviously not only about health, as this boast indicates: ‘Covid Pass is an award-winning DHSC programme undertaking a complex transition while continuing to deliver a vital citizen service in a changing health landscape.’
Digital surveillance here we come. But is it even more than that? Why are governments around the world so determined to inject us with repeated vaccines against a mostly mild and unremarkable respiratory virus? Are we being genetically engineered, and for what purpose? I can’t answer that, but clearly more jabbing is planned. In some countries the vaccine passport had slots for eight or ten doses, like a coffee loyalty card. Vast sums have been spent on stocks of Pfizer and Moderna vials.
I wonder how the interview panel would answer if applicants ask how many jabs they would be expected to take. Or is this post at a level high enough for vaccine immunity? For the plebs, however, Covid will be very long indeed.
Government Mortality Data Just Released – Unbelievable Stuff!
Ivor Cummins |June 3, 2022
Title says it all, wait til you see the data! – we finally have the full Central Statistics Office data, published from the Govt for 2020 and 2021 – revelations abound! Graham Neary’s CSO Data: https://we.tl/t-kqccozGUT5
Also some key references here including Hopkins https://thefatemperor.com/wp-content/…
Live from Mainstream GB News Studio! A super discussion on Pandemic Anxiety and More
NOTE: My extensive research and interviewing / video/sound editing and much more (including expensive travel to enable these media appearances!) does require support – please consider helping if you can with monthly donation to support me directly, or one-off payment: https://www.paypal.com/donate?hosted_…
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Doctors Sue FDA, Allege Crusade Against Ivermectin ‘Unlawfully Interfered’ With Their Ability to Treat Patients
The Defender | June 6, 2022
Three physicians are suing the U.S. Food and Drug Administration (FDA) for launching what they allege is a “crusade” against ivermectin as a treatment for COVID-19 that “unlawfully interfered” with the doctors’ ability to practice medicine.
In a lawsuit filed June 2, Drs. Robert L. Apter, Mary Talley Bowden and Paul E. Marik argued the FDA acted outside of its authority by directing the public, including health professionals and patients, to not use ivermectin — even though the drug is fully approved by the FDA for human use.
The suit, filed in the U.S. District Court, Southern District of Texas, Galveston Division, also names the U.S. Department of Health and Human Services (HHS), HHS Secretary Xavier Becerra and Robert Califf, acting FDA commissioner.
According to the complaint:
“The FDA generally cannot ban particular uses of human drugs once they are otherwise approved and admitted to the market, even if such use differs from the labeling — commonly referred to as ‘off-label’ use.
“The FDA also can not advise whether a patient should take an approved drug for a particular purpose. Those decisions fall within the scope of the doctor-patient relationship.
“Attempts by the FDA to influence or intervene in the doctor-patient relationship amount to interference with the practice of medicine, the regulation of which is — and always has been — reserved to states.”
The plaintiffs said their lawsuit isn’t about whether ivermectin is an effective treatment for COVID-19. It’s about who determines the appropriate treatment for each unique patient and whether the FDA can interfere with that process.
In their complaint, they site an FDA publication, “Why You Should Not Use Ivermectin to Treat or Prevent COVID-19,” and tweets from the FDA — including one implying that ivermectin is intended only for animals — among examples of the FDA discouraging the use of ivermectin.
The plaintiffs also argued if the FDA is allowed to interfere with the practice of medicine now, using the pandemic as a cover, “this interference will metastasize to other circumstances, destroying the carefully constructed statutory wall between federal and state regulatory powers, and between the FDA and the professional judgment of health professionals.”
“This lawsuit, brought by three eminently qualified physicians, is a welcome development,” said Mary Holland, Children’s Health Defense president and general counsel.
Holland told The Defender :
“These doctors rightfully assert that the FDA, assisted by corporate media, have unlawfully interfered in the doctor-patient relationship and the appropriate treatment for individual patients. Regulating the doctor-patient relationship is an area of well-established state, not federal, law.
“I hope these plaintiffs will enjoin the FDA from continuing to restrict access to ivermectin and from penalizing healthcare practitioners who use this licensed drug for their patients.”
The plaintiffs: well-respected in their field, high success rate treating COVID patients
Apter, who is licensed to practice medicine in Arizona and Washington and has a COVID-19 patient survival rate of more than 99.98%, was referred to the Washington Medical Commission and Arizona Medical Board for disciplinary proceedings for prescribing ivermectin to treat COVID-19.
In a press release, Apter said, “If doctors are freed to treat patients according to their best judgment and unprejudiced evaluation of the medical literature, many thousands more deaths and serious disabilities will be averted.”
Apter said the FDA’s pronouncements against the use of ivermectin “have been the basis for disciplinary actions against doctors, interfere with the doctor-patient relationship, and have had a severe chilling effect on the use of life-saving medication for a deadly disease.”
In the lawsuit, Apter argued that government pressure, “largely through the FDA,” also led pharmacies — especially in large corporate chains — to refuse to fill ivermectin prescriptions for COVID-19, because that position is supported by the FDA.
Bowden, who according to the lawsuit has 40 years of experience in emergency medicine, began recommending ivermectin to treat COVID-19 in early 2020. She treated more than 3,900 patients for COVID-19, with a success rate of over 99.97%.
She said the FDA’s actions regarding ivermectin, specifically its directives to stop using the drug to treat COVID-19, harmed Bowden’s ability to practice medicine and treat patients.
Bowden’s employer, Houston Methodist Hospital, last year forced her to resign by suspending her privileges for spreading “COVID misinformation.”
Bowden said she is “fighting back — the public needs to understand what the FDA has done is illegal, and I hope this suit will prevent them from continuing to interfere in the doctor-patient relationship.”
In an interview earlier this year with The Defender, Bowden said she was all for the COVID vaccines when they first came out — it was only when she started seeing what was happening with all the breakthrough cases that she wondered, “Why am I seeing so many COVID cases among the fully vaccinated?”
Then her patients began having adverse reactions. “If I hadn’t seen that firsthand, I would still think the vaccine was the way to go,” she said.
As the pandemic evolved, Bowden developed protocols for preventing and treating COVID patients. She said she’s seen excellent results.
“The basis of it is ivermectin,” she said. “And also vitamins C and D, quercetin and zinc, and black seed oil. It’s nothing complicated — and it’s just like with anything in medicine — not one size fits all — protocols are guidelines.”
The controversy over prescribing ivermectin was initially “intimidating and isolating,” she said. “I thought I was a little bitty island in a huge ocean, and now I realize that I’m part of at least half a continent.”
Marik, author of more than 750 publications, was professor of medicine and chief of pulmonary and critical care medicine at Eastern Virginia Medical School (EVMS) in Norfolk, Virginia, from 2009 through 2021. He also served as a director of the intensive care unit at Sentara Norfolk General Hospital.
He developed a protocol for EVMS for treating COVID-19, called the EVMS COVID-19 Management Protocol, which included the MATH+ Protocol.
However, according to the lawsuit, Marik was forced to resign from his positions at EVMS and Sentara Norfolk General Hospital for promoting the use of ivermectin — “as well as other safe, cheap, and effective off-label FDA-approved drugs” — to treat COVID-19 following the FDA’s attempts to stop use of those drugs for that purpose.
Marik alleged in the lawsuit that refusing to allow patients to receive effective early treatment for COVID-19 “led to innumerable hospitalizations and deaths, and caused extreme distress for patients, their families, and health professionals.”
Boyden, Gray & Associates, a Washington, DC-based law firm, is representing the plaintiffs.
Ivermectin was developed in the 1970s as a veterinary medicine to treat parasitic diseases in livestock, but a decade or so later was hailed as a “wonder drug” and received approval for human use as a therapeutic against diseases such as river blindness — or onchocerciasis — and lymphatic filariasis, according to Newsmax.
Since 1987, it has been used safely in 3.7 billion doses worldwide. William Campbell and Satoshi Omura won the 2015 Nobel Prize in Physiology or Medicine for their research on the drug.
Studies show ivermectin is associated with lower COVID-19 death rates, but the FDA — with help from mainstream media — continues to state the drug is ineffective for treating COVID.
© 2022 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.
Fauci’s COVID origins coverup spook has resurfaced to misdirect us about the origin of money pox
By Meryl Nass, MD | June 7, 2022
Andrew Rambaut (pronounced Rambo—and like Rambo, he is still in the ring, fighting for the globalists, when he should have taken his toys and slunk away long ago—after being beaten up as one of the stooges who produced the fake Nature Medicine paper on COVID’s origins) has long been associated with a group of virology spooks in Tony Fauci and Jeremy Farrar’s network. The field of evolutionary biology is supposed to tell you where new viruses have come from. But of course, it has been kidnapped to provide specious explanations when the biowarriors need to try and explain their concoctions as having natural origins.
Rambaut was also used to dispute the origins of HIV (as described in my friend Ed Hooper’s book The River ) while teamed up with Eddie Holmes, another Fauci flunkie, more than 20 years ago.
Republican members of Congress want to know what Fauci and his henchmen were up to when they concocted a fake natural origin for COVID, as revealed in the Fauci emails.
Rambaut was one of the 5 authors of that paper, and the paper was highly effective for a bit over one year at keeping a lid on COVID’s lab origin. As the members of Congress wrote:
Andersen and three other doctors on this teleconference [including Rambaut] later published a paper titled “the proximal origin of SARS-CoV-2 in Nature Medicine on March 17, 2020. This paper was highly influential in shaping our nation’s response to the pandemic. In the paper, the doctors concluded that “…we do not believe that any type of laboratory-based scenario is plausible.”[11]
… The Andersen paper led the narrative away from COVID-19’s potential lab origins. As Americans, we are deeply concerned by the appearance of discrepancies that largely influenced our understanding and approach to this virus. As Representatives of the American people, we owe it to them to seek and expose the truth about this virus’ origins wherever those efforts may lead.
Now Rambaut has popped up again, like a jack-in-the-box, to explain how the unexplainable 50 single nucleotide polymorphisms (SNP mutations) could have happened naturally. He has another bold theory! There was an evolutionary jump!
And Rambaut proffered yet another theory: the virus has been spreading in humans for years; we just didn’t notice it.
Below is a paper published by Portuguese researchers discusing the newly discovered mutations in money pox. They mention Rambaut’s theory, and Rambaut himself provides the first comment below the paper.
Spooks like Dr. Rambaut don’t do this dirty work for nothing. Just last month, he was made a fellow of the Royal Society.
From Wikipedia:
Science reported on 11 January 2020 that Rambaut was the first to publish the genome of the COVID-19 coronavirus after it was sent to him by Edward C. Holmes.[11][12] Holmes has said that it “took 52 minutes from receiving the code [from his Chinese colleague Professor Yong-Zhen Zhang] to publishing” on Virological.[13][14] The BBC Horizon episode The Vaccine stated: “When Chinese scientists published the genetic sequence of a mystery new virus on January 10th 2020, vaccine scientists around the world immediately sprang into action”.[15]
Rambaut was one of the authors of the scientific paper The proximal origin of SARS-CoV-2,[16] which concluded that “SARS-CoV-2 is not a laboratory construct or a purposefully manipulated virus”.
Rambaut is an attendee of the UK’s Scientific Advisory Group for Emergencies (SAGE).[17]
Perhaps someone else can look up his recent research grants. Were they from NIH or Wellcome? Being rewarded royally with other peoples’ money is another characteristic of the virology spook group.
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TV Drama Review
Japanese drama projects Japan’s wartime atrocities onto Chinese characters
Global Times | October 25, 2026
By portraying Chinese characters as perpetrators of ruthless violence while casting Japanese Self-Defense Forces (SDF) intelligence operatives as defenders, the season 2 of the Japanese drama Vivant has recently drawn criticism from Chinese netizens, who argue that its depiction turns historical reality on its head while ignoring Japan’s wartime atrocities.
The TBS drama series – a spy suspense story in which an alleged unofficial intelligence unit of the SDF operates across the globe — has attracted a passionate fanbase. Its currently airing season 2 opened with a household rating of 18.8 percent, the highest for a TV drama this year, according toa commentary article by Japanese media Toyo Keizai.
What draws attention is the portrayal of the enemies in the series, the article noted. Scenes in which the Chinese organization subjects kidnapped members of the SDF unit to brutal torture are repeated with unrelenting intensity.
It is rare for Japanese TV dramas to explicitly portray a real-life country as the enemy, the article noted.
Japanese Prime Minister Sanae Takaichi also made a reference to the drama, saying that she has been recording Vivant and hopes to binge-watch it over the year-end and New Year holidays, according to Japanese media outlets.
China’s CCTV News report on Sunday revealed that the drama features scenes in which Chinese personnel cut off the fingers of and stab Japanese intelligence operatives in the abdomen. Such acts bear striking similarities to the torture inflicted on Chinese nationals by invading Japanese troops during the World War II.
The drama distorts the truth by attributing these atrocities to modern Chinese characters. Beneath the surface, it subtly glorifies Japan’s cross-border overseas operations, blurs the functional boundaries of the SDF and implicitly promotes an expansionist narrative, per CCTV News. … continue
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