Recently, Medpage Today made sure to feature an article on how Reuters faced backlash after publishing an article stating that ivermectin was “effective” against Omicron in phase III trials, when what really happened was a Japanese company issued a press release stating ivermectin showed an “antiviral effect” against Omicron and other variants in joint non-clinical research.

The article further pigeon-holes ivermectin by calling it an “anti-parasitic drug” when research HAS shown it’s potent anti-viral effects by blocking importin, thereby preventing nuclear import and inhibiting viral access to cell nuclei. Many drugs currently on the market have multiple modes of action. Ivermectin is one such drug. It is both antiparasitic and antiviral.

The complete truth just isn’t convenient as an effective treatment would nullify COVID gene therapy injections.

They then bemoan that Twitter users state the uncorrected version will live-on on COVID conspiracy sites, as if Twitter is the fount of all knowledge.

The information that didn’t make the article is the fact that a city-wide, prospective, observational study of over 200,000 subjects found ivermectin substantially lowered infection, hospitalization, and mortality rates. 

Results:

The regular use of ivermectin led to:

  • a 68% reduction in COVID-19 mortality (25 [0.8%] versus 79 [2.6%] among ivermectin non-users; RR, 0.32; 95% CI, 0.20-0.49; p < 0.0001)
  • a 70% reduction in mortality when adjusted for residual variables (RR, 0.30; 95% CI, 0.19-0.46; p < 0.0001)
  • a 56% reduction in hospitalization rate (44 versus 99 hospitalizations among ivermectin users and non-users, respectively; RR, 0.44; 95% CI, 0.31-0.63; p < 0.0001)
  • a 67% reduction in hospitalization rate when adjusted for residual variables (RR, 0.33; 95% CI, 023-0.66; p < 0.0001)

While this study focused on prophylaxis, it’s important to note ivermectin’s obvious anti-viral qualities, which is the important take away. Proponents of ivermectin and HCQ have been quite clear that the earlier the treatment is initiated, the better the outcome (similarly to Lyme/MSIDS). This well written article called the Spartacus Letter explains:

  • the pathophysiology of COVID
  • the vast majority of COVID-19 cases are mild and do not cause significant disease
  • ventilation is killing patients
  • correct treatment for severe COVID-19 related sepsis is non-invasive ventilation, steroids, and antioxidant infusions
    • N-acetylcysteine, melatonin, fluvoxamine, budesonide, famotidine, cimetidine, and ranitidine are all antioxidants

But the most important information contained in the Spartacus Letter is the following:

Because of the way they are constructed, Randomized Control Trials will never show any benefit for any antiviral against COVID-19. Not Remdesivir, not Kaletra, not HCQ, and not Ivermectin. The reason for this is simple; for the patients that they have recruited for these studies, such as Oxford’s ludicrous RECOVERY study, the intervention is too late to have any positive effect.

So there you have it. RCTs will NEVER show benefit for ANY antiviral due to the way the studies are constructed.
Corrupt public health agencies know this.  They are banking on it.

To make their narrative work, they must ignore research that isn’t a RCT, like the aforementioned and numerous others:  https://ivmmeta.com/

Regarding ivermectin:

Evidence base used for other COVID-19 approvals
Medication Studies Patients Improvement
Molnupiravir (UK) 1 775 50%
Budesonide (UK) 1 1,779 17%
Remdesivir (USA EUA) 1 1,063 31%
Casirivimab/i.. (USA EUA) 1 799 66%
Ivermectin evidence 78 85,743 64% [57‑70%]

As is clearly seen from the table, the evidence for ivermectin utilizes 78 studies and nearly 86,000 people vs. only ONE study and a fraction of the patients for drugs receiving emergency use authorization (EUA).  It is also clear that ivermectin gives greatest improvement over those pushed by mainstream medicine and corrupt public health ‘authorities’.

Please see this excellent video on the powerful players colluding together to suppress ivermectin, as well as a revealing transcript of a conversation with Dr. Andrew Hill, who admitted to caving to pressure to downplay the benefits of ivermectin as a COVID treatment.

The clinical studies that do exist, and the consilience of the real-world data (RWD), show that early use of ivermectin reduces mortality by somewhere between 50 and 85%. ~ Dr. James Lyons Weiler

As the World Tribune reports:

In a recent Zoom call, Dr. Pierre Kory of the Front Line COVID-19 Critical Care Alliance outlined numerous details showing the World Health Organization (WHO) knowingly suppressed data on the effectiveness of ivermectin against the virus in order to benefit the vaccine interests of Big Pharma.

“It’s criminal,” Kory said. “It’s literally criminal.” The drug “could have saved half a million lives this year if it had been approved.”

The WHO, Kory contends, is simply taking part in the tactics of a time-worn “Disinformation Playbook.” The term was coined by the Union of Concerned Scientists 50 years ago to describe the strategies corporations have developed over decades to “attack science when it goes against their financial interests.”

According to the Tribune, this disinformation strategy has five parts:

  1. The Fake – Conduct counterfeit science and try to pass it off as legitimate research.  Please see this excellent article showing 5 studies where researchers present conclusions that don’t match the data.
  2. The Blitz – Harass scientists who speak out with results reviews inconvenient for industry.
  3. The Diversion – Manufacture uncertainty about science where little or none exists.
  4. The Screen – Buy credibility through alliances with academia or professional societies.
  5. The Fix – Manipulate government officials or processes to influence policy inappropriately.

Medpage Today misses the point entirely and is only serving as a Big Pharma shill to the demise of sick patients.  It is actively taking part in the disinformation strategy outlined above. 

A_Literature_Review_and_Meta_Analysis_of_the_Effects_of_Lockdowns

January 2022

By Jonas Herby, Lars Jonung, and Steve H. Hanke

John Hopkins Institute for Applied Economics, Global Health, and the Study of Business Enterprise

Abstract
This systematic review and meta–analysis are designed to determine whether there is empirical evidence to support the belief that “lockdowns” reduce COVID–19 mortality. Lockdowns are defined as the imposition of at least one compulsory, non–pharmaceutical intervention (NPI). NPIs are any government mandate that directly restrict peoples’ possibilities, such as policies that
limit internal movement, close schools and businesses, and ban international travel. This study employed a systematic search and screening procedure in which 18,590 studies are identified that could potentially address the belief posed. After three levels of screening, 34 studies ultimately qualified. Of those 34 eligible studies, 24 qualified for inclusion in the meta–analysis.
They were separated into three groups: lockdown stringency index studies, shelter–in–place–order (SIPO) studies, and specific NPI studies.

An analysis of each of these three groups support the conclusion that lockdowns have had little to no effect on COVID–19 mortality.

More specifically, stringency index studies find that lockdowns in Europe and the United States only reduced COVID–19 mortality by 0.2% on average. SIPOs were also ineffective, only reducing COVID–19 mortality by 2.9% on average. Specific NPI studies also find no broad–based evidence of noticeable effects on COVID–19 mortality.

While this meta–analysis concludes that lockdowns have had little to no public health effects, they have imposed enormous economic and social costs where they have been adopted.

In consequence, lockdown policies are ill–founded and should be rejected as a pandemic policy instrument.

________________

Go here for an excellent article and news video titled: “The CDC is Finally Recognizing ‘Natural Immunity’ – Legislators Should Follow Suit”

Not exempting those with prior infection was always unfair; now it is unscientific as well.

https://childrenshealthdefense.org/defender/cdc-natural-immunity-trumps-vaccine-immunity/

CDC Admits Natural Immunity Trumps Vaccine Immunity — 5 Months After Touting Vaccines as Superior

Five months after issuing a statement that vaccine immunity protects against COVID better than natural immunity, the Centers for Disease Control and Prevention sent a report showing the opposite is true, at least when it comes to the Delta variant.

A Jan. 19 report from the Centers for Disease Control and Prevention (CDC) showed natural immunity against COVID was at least three times as effective as vaccination alone at preventing people from becoming infected with the Delta variant.  (See link for article)

Important quote regarding higher hazard rates for hospitalization in the vaxxed:

“This is potentially a concerning finding in that it suggests the vaccine could be interfering with natural immunity,” Setty said.

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https://www.clarkcountytoday.com/news/natural-immunity-gets-another-boost-from-two-new-u-s-studies/

Natural immunity gets another boost from two new U.S. studies

CDC and Johns Hopkins studies show strength and duration of natural immunity protection

Two newly released studies show the power of natural immunity following recovery from COVID-19 sickness. The Centers for Disease Control and Prevention (CDC) says:

“previous SARS-CoV-2 infection also confers protection against severe outcomes in the event of reinfection.”

Johns Hopkins found that natural immunity developed from prior variants reduced the risk of infection with the Omicron variant.  (See link for article)

Summary:

  • natural immunity was six times stronger during the Delta wave than vaccination 
  • Dr. Makary states that “hybrid immunity” (“vaccinated” & infected) increases immunity by 3.8%, while Dr. Urso, on the other hand, states there’s no such thing as “super immunity.”  Natural immunity is robust, long-lasting, and sufficient. 
  • Makary believes we aren’t seeing new “vaccinations” because people are hardened by excessive government policies and are choosing to forgo the shots. He also states “no healthy child has ever died of COVID that we know of.”
  • The Omicron wave in Africa subsided quickly with modest hospitalizations because close to 80% had been previously infected by variants.
  • The CATO institute weighed in and stated that “universal vaccine mandates are irrational in ignoring naturally acquired immunity from infection and recovery…..If OSHA had reviewed the medical and scientific literature regarding the relative protection efficacy of natural immunity compared to “vaccination”, it is unlikely the agency would be successful in establishing a factual basis for forced “vaccination” of COVID-recovered individuals.  Given the trivial – if any – benefit to either the individual or the public from compelled “vaccination” of Covid-recovered individuals, that evidence of elevated adverse effects requires an especially high standard of proof by regulators to overcome.”
  • Dr. Makary states, “By firing staff with natural immunity, employers got rid of those least likely to infect others.” “It’s time to reinstate those employees with an apology.”
  • Makary states it’s time to rehire the fired for three reasons: it was unfair to begin with, we have therapeutics, and many have natural immunity. “The risk of somebody who has natural immunity getting hospitalized is 3 per 10,000,” which is identical to the risk of someone with hybrid immunity – so getting a booster did NOTHING to change hospitalization numbers.
  • Makary noted that public health officials are falsely reporting higher numbers of COVID deaths than reality shows, and cases have declined steeply.
  • It’s normal to have a massive influx of patients every winter from a number of respiratory pathogens, the problem this time is a massive staffing shortage.  One in five health care workers have left. 

Washington State was so short-staffed they told workers who had COVID to come back into work – even with symptoms.

  • There’s only been ONE death in 52,000 Omicron cases in the Kaiser CA study, which is LOWER than influenza.
  • The article then reported on a North Carolina man who said a hospital refused to carry out a kidney transplant because he’s unvaccinated against COVID-19. He is willing to “die free” rather than comply with their vaccine requirement. He’s had the coronavirus twice before and believes getting the vaccine should be a personal choice, not a requirement.  The hospital doesn’t care about science and is holding its ground. Sadly, this has been happening globally.  A three year old from Cyprus was also refused lifesaving surgery in three countries because his parents weren’t vaxxed.  Go here to send an email to your members of Congress to stop this violation of medical ethics.
  • Noah Carl noted in his review of the Danish study, that there’s no obvious need for people who have recovered from COVID to get vaccinated.

“The tricky part may be getting this message through to politicians.”

Illogical COVID madness continues…..

For more:

https://www.liebertpub.com/doi/abs/10.1089/vbz.2021.0085?journalCode=vbz

Established Populations of Rickettsia parkeri-Infected Amblyomma maculatum Ticks in New York City, New York, USA

Published Online:https://doi.org/10.1089/vbz.2021.0085

Objectives: We sought to determine the habitat associations and pathogen status of Amblyomma maculatum (Gulf Coast tick) ticks in New York City (NYC), New York, USA, a newly expanded portion of their range.

Methods: We collected 88 ticks from two NYC parks on Staten Island, one of the five boroughs of NYC, and compared our findings with similar habitat in Brooklyn, New York during the same time period (April 30–September 1). We tested 76 for pathogens.

Results: We found adult and immature ticks in native and invasive grasses at Freshkills and Brookfield parks on Staten Island. No A. maculatum ticks were found in Brooklyn.

  • 52.6% of ticks tested were infected with Rickettsia parkeri—the etiological agent of R. parkeri rickettsiosis.

Conclusions: This high rate of R. parkeri in a dense urban center is of concern to the medical community, who should be aware of this species’ presence and the symptoms of R. parkeri rickettsiosis.

_________________
For more:

https://mta.ca/about/news/cats-and-cars-help-scientists-study-lyme-disease-fri-01282022-0859

Cats and cars help scientists study Lyme disease

28 Jan 2022
Study from Mount Allison University researchers uses citizen science to find a new source of Lyme disease bacteria in New Brunswick mice

SACKVILLE, NB – A new study from Mount Allison University, aided by cats and cat owners, is shedding light on a new source of Lyme disease bacteria in the Maritimes and how the Lyme disease pathogen in transmitted in wildlife.

Mount Allison University biology professor Dr. Vett Lloyd and graduate student Chris Zinck recently published a paper, Borrelia burgdorferi and Borrelia miyamotoi in Atlantic Canadian wildlife, in the peer-reviewed journal PLOS ONE.

Lloyd and Zinck partnered with local veterinarians and cat owners to collect wildlife specimens and study them for zoonotic diseases – diseases such as Lyme disease that are transmitted from wildlife to humans. In this latest study, Lloyd, who heads Mount Allison’s Tick Lab, and Zinck have found a new wildlife species, the jumping mouse, that can carry Lyme disease in New Brunswick. The pair also discovered that one of the types of Lyme disease bacteria can be transmitted through the placenta to the young in that mouse species.

“We know that Lyme disease is abundant in New Brunswick wildlife,” says Lloyd. “But we didn’t know how abundant it was in wild animals in the province and these findings raise more concerns about the potential risks of Lyme disease in our region.”

To collect wildlife specimens, researchers used a Citizen Science approach, enlisting the assistance local cats and motorists in providing a large number of mice, voles, shrews, squirrels, porcupines, and other animals, to study.

Lloyd came up with the community-based approach at her home with her cat Entropy, a calico who hunts with surgical precision.

“As I looked at yet another one of Entropy’s ‘gifts’ on the front step, I wondered if there was a way for these little lives to contribute to science,” says Lloyd. “I had the same thought on my drive into work along the TransCanada highway each day, seeing animals on the side of the road.”
Zinck, who completed both his undergraduate and master’s degrees at Mount Allison and is currently completing his PhD at the University of Saskatchewan, also hit the road in the name of science. With a safety vest and permits in tow, he collected and dissected several hundred accidentally killed wild animals, finding both the known Lyme disease bacteria, Borrelia burgdorferi, and a different kind, Borrelia miyamotoi, in specimens.

“This work is important for the health of people and their pets as Borrelia miyamotoi infection would not be detected by the standard Lyme disease tests,” says Lloyd. “Even more surprisingly, we found that an infected jumping mouse mother had passed the infection on to her fetuses. This has implications for the health of wildlife and although few people would worry too much about the health of wild mice, it does have implications for a rapid increase in infected mice and the possibility that an infected human mother could pass on the infection to her child.”

Lloyd and Zinck hope that this work will help people realize how closely people and wildlife are connected and that the community can participate in advancing science.

The article, published on Jan. 22, is available to the public on journal’s website: PLOS ONE https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0262229

https://popularrationalism.substack.com/p/what-are-the-real-risks-of-genetic?

What Are the Real Risks of Genetic Manipulation Technology? Part 1.

The public must have a say in its own future. Profiteering technocrats must not decide for all of us.

Here’s question I recently received:

Dear Dr. Jack:

Are you concerned about gene modification technology?

Yes, I am deeply concerned about gene modification technology. Like all tech, it can be used for good and evil. Before I go into the ways it can be abused and lead to harm, we have to distinguish between two type of gene modification technology: somatic gene modification technology (SGMT, non-heritable) and genetic modification technology (heritable). In Part 1 of this series, I will focus on SGMT.

Somatic gene modification technology (SGMT) changes genes in an individual in a way that is not passed on to future generations. There are some promising applications of this technology, and most who have looked into the risks of gene modification tech seriously take the position that when the genetic modification reverses a disease state – as would be possible in certain forms of blindness, cystic fibrosis and muscular dystrophy – without increasing the risk of other medical issues – such as cancer – then gene modification technology is a good thing. The genetic information would be integrated in limited number of cells in a person of a particular type, such as the retina, or in specific lung tissue. (Read about Gene Therapy for Cystic Fibrosis).

This use could be seen as as curing individuals of conditions they inherited. The problem is that society will have to decide where to draw the line between reversing a negative condition, and merely enhancing a human being (improvement), such as enhancement of athletic performance (gene doping). Let’s call this problem “The First Slippery Slope” (you’ll see why in a minute).

Knowing how big Pharma and big medicine operate as well as I do, my crystal ball tells me exactly what could happen over the next 5-30 years with SGMT:

  1. It will be allowed for use in individual to reverse inherited, deadly or painful conditions.
  2. A black market of genetic improvement “therapies” will spring up. It will be extremely expensive, and only the elite will be able to afford these “improvements”. These will include athletes, and those who have adopted “transhumanism”. There’s a small chance (around 1%) that this is already happening. Early adopters risk cancer due to off-target modifications: unintended mutations, of the type that has been seen in the Crispr/Cas9 gene editing system. These problems are being addressed.
  3. The medical community will begin to pathologize conditions where the technology could be used to improve human beings. “Conditions” with fancy names like muscular asthenia will be contrived. Dr. Atlas will provide an injection of an mRNA with a retrovirus that infects muscle cells and causes more responsiveness to ambient growth hormone, and we’ll see a return to ads like these:

The Second Slippery Slope will be brought on by market forces that use the fixtures of societal influence and power to bring about compliance. This is not mere theory; we’ve see this before with voluntary vaccination programs that become mandated. Via a combination of legislation and PR to induce voluntary trust, those who will benefit financially will abuse the public’s trust and bring about, one way or the other, enforcement to maximize their market share without adding anything of real additional competitive value to an open market (this is also called “Rent-Seeking”).

Another Second Slippery Slope, from Meuhlbacher and Kirchler (2010).

  1. Somatic gene modification used to reduce the risk of heritable risk of early onset dementia and neurodegeneration will be allowed, but then a route to increase intelligence will be found via genetic modification. At first it will be used by the elite – those who have funds for this boutique-level genetic improvements. But when Pharma recognizing the market is much larger, medical terms such as hypointelligence will be normalized by pathologizing below-level intelligence levels. The obedient media will inform the public that it’s now considered unethical to not vaccinate your newborn child against hypointelligence, and well-meaning, loving parents who comply will help change the cultural norm.
  2. Social behavioral gene “therapy”. Scientists have already identified over 40 genes associated with aggression in humans and mice. One study reports a “warrior gene” – MAOA-L gene – that predicts whether a person will be aggressive when “provoked”. Someone will find a way to reduce aggression in mice via gene therapy. Studies will be done involving mice put under stress that causes them to be violent toward each other, to demonstrate that the treated mice won’t harm other mice. Human trials will be done on the most violent criminals and on children with autism who self-harm or hurt others. Criminals convicted of violent acts will be offered a choice: prison, or social behavioral gene therapy. The promise of a future without crime will be seen as looming, just over the horizon, and parents will be forced to test their children for evidence of “genetic aggression syndrome” and transfect their children to help eliminate violent crime from society. The specific therapy will likely be “gene inhibition therapy”, in which a gene that causes the brain to produce silencing RNA that shuts down the production of proteins associated with aggression will be transfected into infants.
  3. Somewhere along the way, an Elon Musk-like figure will emerge that champions genetic modification to improve our species. Alternatively, in these Regulatory States of America, it will be more likely than not be a regulatory committee in HHS that votes to approve (and thereby mandate) genetic modification therapies. The committee will be infiltrated by people with direct conflicts of interests and ties to companies that own the patents on genetic modification therapies. He, she, or it will become, like The High Evolutionary of Marvel Comics, might even be early adopters – those who has demonstrated the utility of brain-enhancement by gene modification. Being super-intelligent, they will garner followers who take it upon themselves to decide the evolutionary fate of humanity.

    Well, I don’t know if it’s me, or that I found Marvel Comic scenarios that match my predictions so well. I’ve scared myself enough already with this Part 1 of this series, and I’ve just started.

You can read more of my prognostication of this type more formally approached in this peer-reviewed analysis in Biological Theory, which I published in 2021.

Lyons-Weiler, J. 2021. Who are We, and Who (or What) Do We Want to Become? An Evolutionary Perspective on Biotransformative Technologies. Biological Theory.

PS I’m currently in Facebook jail for a week for calling out WashPo for attributing causality of Ivermectin to side effects based on phone calls to poison control center… instead of citing peer-reviewed clinical research studies. So please do me a favor and share this article across Facebook, Twitter, MeWe, Gettr and help right the wrongs of censorship.

If you’re not yet a paid subscriber, please consider pitching in. Your $7 per month paid subscription will power articles like these.

___________________

**Comment**

Before you write this off as a piece of science fiction, mRNA technology is already being promoted for cancer, HIV, autoimmune disorders, genetic diseases, as well as in Lyme-land:  https://grist.org/health/how-mrna-technology-could-create-a-new-vaccine-against-ticks/

SUMMARY:

  • The article predictably starts with the false narrative that the climate is behind tick proliferation.  Not a word is uttered on our government’s role in spreading ticks and disease.
  • The article also predictably mentions that approximately 500,000 are diagnosed with Lyme but fail to mention that this is a YEARLY rate and doesn’t touch the millions chronically infected.
  • It does state that there is no coordinated national response like for STDs or COVID but fails to mention that there is plenty of controversy on Lyme being sexually transmitted.  Better to stick to the script.
  • But the high numbers and the lack of national response is ALWAYS utilized for the vaccine angle.  ALWAYS.  And it’s getting mighty old.
  • A vaccine, according to the author who is just another shill for Big Pharma, is the magic pill and would solve all our problems.  If only.
  • Of course they repeat the oft repeated mantra that some crazies complained that the last Lyme vaccine caused side effects – but had negligible evidence.  Please go here for the ‘negligible’ evidence.
  • Superheros from Yale are trying to revive a Lyme vaccine that of course looks nothing like the last one. (For all you crazies who are actually worried about such nonsense)
  • And guess what?  The Yale “dream team” is using messenger RNA, the same stuff that Pfizer and Moderna are using in their COVID “vaccines” which don’t stop transmission or infection, have caused more adverse reactions and death than another other vaccine in the history of VAERS, and are actually causing antibody dependent enhancement (ADE) which is making the “vaccinated” more prone to illness with COVID variants.  “Vaccine” failure has been proven. But, who wants to be a Debbie Downer?
  • Despite the fact the mRNA shot for Lyme hasn’t even been tested in humans yet, everything about the article makes it appear to be the answer to all our woes. (Except for those crazies who question everything)
  • The article ends by promoting a national response to “take the responsibility off of individual patients,” who are currently responsible for buying their own DEET, protective clothing, and doing tick checks.

No thanks. I’d rather take responsibility for myself than trust organizations that are so riddled with conflicts of interest they’ve forgotten long ago what truth actually sounds like.