Aug 232021
 August 23, 2021  Posted by at 9:24 am Finance Tagged with: , , , , , , ,

Vasily Polenov Moscow courtyard 1878


The FDA Is Begging You Not to Take Horse Dewormer for Covid-19 (RS)
How Does Covid-19 Affect The Brain? (NatGeo)
Potential Use Of Ivermectin For Treatment And Prophylaxis Of SARS-CoV-2 (SD) /span>
Ivermectin for Prevention and Treatment of COVID-19 Infection (AJT)
Stop The Mandates Or People Die (Denninger)
Molecular Determinants of SARS-CoV-2 Variants (Cell)
Biden Team’s Misguided And Deadly Covid-19 Vaccine Strategy (WT)
100s Of Doctors Sign Open Letter: Need Debate On ‘Flawed Covid Guesses’ (Exp.)
Rescue Dogs Shot Dead By NSW Council Due To Covid-19 Restrictions (SMH)
Afghan Staff At US Embassy Losing Faith In Evacuation Efforts (NBC)
White House Announces They’ve Lost Kamala Harris (BBee)





A drug safely used by an estimated 3 billion people has been relabeled a horse dewormer. This is a dangerous campaign. Lives are being lost.

The FDA Is Begging You Not to Take Horse Dewormer for Covid-19 (RS)

“You are not a horse. You are not a cow,” the Food and Drug Administration tweeted on Saturday alongside a link to a page on their website explaining “Why you should not use Ivermectin to treat or prevent Covid-19.” Why? Because Ivermectin, a medication usually reserved for deworming livestock, is responsible for a spike in poison control calls in Mississippi as people duped by conspiracy theories have purchased the drug and ingested it, hoping it will treat or prevent Covid-19 — something the drug is not proven to do. According to an alert issued by the Mississippi Department of Health on Friday, 70 percent of all recent calls to poison control in the state “have been related to ingestion of livestock or animal formulations of ivermectin purchased at livestock supply centers.”

Although most callers (85 percent) only reported mild symptoms, one person was advised to seek additional treatment. “Animal drugs are highly concentrated for large animals and can be highly toxic in humans,” the alert said. Ivermectin is sometimes used in humans to treat parasites or scabies, but in much smaller doses than are given to livestock. The calls have clearly baffled health officials in the state. “I think some people are trying to use it as a preventative which is really kind of crazy,” Dr. Thomas Dobbs, Mississippi’s state health officer, said. “So please don’t do that.”

“You wouldn’t get your chemotherapy at a feed store,” Dobbs added. “You wouldn’t treat your pneumonia with your animal’s medication. It can be dangerous to get the wrong doses of medication, especially with something meant for a horse or a cow.” But the obvious risks of humans ingesting Ivermectin haven’t stopped people at Fox News — including hosts Laura Ingraham, Sean Hannity, and Tucker Carlson — from dangerously suggesting that it is a safe and effective treatment for Covid-19, as Rachel Maddow pointed out on her Friday night show where she showed clips of Fox personalities pushing the drug consistently over the last six months.

Read more …

Very little is clear. Only thing to do is keep people from being infected. And the vaccines don’t do that: internal document from the C.D.C. states that some 35,000 vaccinated people experience symptomatic coronavirus infections each week..

How Does Covid-19 Affect The Brain? (NatGeo)

If SARS-CoV-2 doesn’t infect brain cells, how is so destructive to cognition? There are two leading hypotheses. The first is that the infection somehow triggers inflammation in the brain. Some COVID-19 patients have suffered encephalitis, or swelling of the brain, which can cause confusion and double vision, and in serious cases, speech, hearing, or vision problems. If left untreated, patients can develop cognitive problems. Viruses like West Nile and Zika can cause encephalitis by directly infecting the brain cells, but how COVID-19 may lead to brain inflammation is less clear. An immune response run amok, known as autoimmunity, might be to blame for some instances of inflammation throughout the body, including the brain.

When the immune system is fighting a disease like COVID-19, it unleashes antibodies to do battle against the infection. But sometimes a person’s immune system becomes hyperactive and instead starts making self-attacking antibodies, known as autoantibodies, which can contribute to inflammation and blood clots. These autoantibodies have been found in the cerebrospinal fluid of COVID-19 patients with neurological symptoms. In the Columbia study, researchers found clusters of microglia—special immune cells in the brain whose job is to clear out damaged neurons—that appeared to be attacking healthy neurons. The phenomenon is called neuronophagia. Most of these rogue microglia were in the brain stem, which regulates heartbeat, breathing, and sleeping.

The researchers think these microglia may get activated by signaling molecules called inflammatory cytokines found in patients with severe COVID-19. These molecules are supposed to help regulate the immune system, but some people’s bodies release too many inflammatory cytokines in response to a viral infection. When researchers at Stanford looked at brain tissue from eight patients who died of COVID-19, they also observed signs of inflammation compared to 14 control brains. Using a technique called single-cell RNA sequencing, they found that hundreds of genes associated with inflammation were activated in brain cells from COVID-19 patients compared to controls.

They also noted molecular changes in the cerebral cortex, the part of the brain involved in decision-making and memory that suggested signaling imbalances in neurons. Similar imbalances have been seen in patients with Alzheimer’s disease. The results were published in Nature in June. A second explanation for cognitive issues is that COVID-19 may restrict blood flow to the brain and deprive it of oxygen. In patients who have died of COVID-19, researchers have found evidence of brain tissue damagecaused by hypoxia, or the lack of oxygen.

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Slow but sure take-up by serious medical journals.

Science Direct (Elsevier). Current Research in Translational Medicine
Volume 69, Issue 4, October 2021, 103309

Potential Use Of Ivermectin For Treatment And Prophylaxis Of SARS-CoV-2 (SD)

Ivermectin performs its function mainly through inhibition of nuclear transport mediated by the imported heterodimer a/b1 , which is responsible for the translocation of proteins of several viral species (Human Immunodeficiency Virus, type 1- HIV1, and Simian Virus 40 – SV40; a known oncogenic DNA), and such translocation is, in turn, essential for viral replication [7,8]. This inhibition appears to affect a considerable number of RNA viruses. It has recently been shown that ivermectin inhibits the replication of the SARS-CoV-2 virus in vitro [8, 9], although it is not clear how this occurs. However, since the causal agent of COVID-19 is an RNA virus, the interference with the same proteins and molecular processes described above can reasonably be expected.

However, these studies were conducted at concentrations substantially higher than expected in the plasma and lungs of humans who receive the approved dose of ivermectin. Pharmacokinetic and pharmacodynamic studies suggest that in order to achieve the plasma concentrations required for in vitro antiviral efficacy, it would be necessary to administer doses up to 100 times higher than approved for human use. However, increasing the dose/kg of body weight may be a strategy to increase efficacy, the increase of the risk of toxicity is not conclusive. Currently, there is a noteworthy absence of efficacious treatments for patients with early infection. Although most patients present mild or moderate symptoms, up to 5-10% may have a bad disease progression, so there is a pressing need for effective drugs to be administered early in the course of infection, even before the appearance of severe symptoms, i.e. when the course of the disease is more modifiable to prevent disease progression and longer-term complications.

In fact, it is known that the earlier the antiviral therapies are started, the greater the benefits for patients, in both influenza [15] and SARS infections [16], as well as, more generally, for all infections. Given the need to find an effective drug that can mitigate the harmful consequences of COVID-19, a large number of studies are being carried out in order to assess the effectiveness of different existing drugs, including ivermectin, with promising results. This narrative review summarizes and outlines the evidence-based effectiveness and safety of ivermectin in patients with SARS-CoV-2 infection, recommending the drug for the treatment of COVID-19 especially in the early stages of the disease.

Read more …

American Journal of Therapeutics: July/August 2021

Ivermectin for Prevention and Treatment of COVID-19 Infection (AJT)

Ivermectin is a well-known medicine that is approved as an antiparasitic by the World Health Organization and the US Food and Drug Administration. It is widely used in low- and middle-income countries (LMICs) to treat worm infections. Also used for the treatment of scabies and lice, it is one of the World Health Organization’s Essential Medicines. With total doses of ivermectin distributed apparently equaling one-third of the present world population, ivermectin at the usual doses (0.2–0.4 mg/kg) is considered extremely safe for use in humans. In addition to its antiparasitic activity, it has been noted to have antiviral and anti-inflammatory properties, leading to an increasing list of therapeutic indications.8

Since the start of the SARS-CoV-2 pandemic, both observational and randomized studies have evaluated ivermectin as a treatment for, and as prophylaxis against, COVID-19 infection. A review by the Front Line COVID-19 Critical Care Alliance summarized findings from 27 studies on the effects of ivermectin for the prevention and treatment of COVID-19 infection, concluding that ivermectin “demonstrates a strong signal of therapeutic efficacy” against COVID-19.9 Another recent review found that ivermectin reduced deaths by 75%. Despite these findings, the National Institutes of Health in the United States recently stated that “there are insufficient data to recommend either for or against the use of ivermectin for the treatment of COVID-19,”and the World Health Organization recommends against its use outside of clinical trials.

Ivermectin has exhibited antiviral activity against a wide range of RNA and some DNA viruses, for example, Zika, dengue, yellow fever, and others.13 Caly et al14 demonstrated specific action against SARS-CoV-2 in vitro with a suggested host-directed mechanism of action being the blocking of the nuclear import of viral proteins that suppress normal immune responses. However, the necessary cell culture EC50 may not be achievable in vivo.16 Other conjectured mechanisms include inhibition of SARS-CoV-2 3CLPro activity(a protease essential for viral replication), a variety of anti-inflammatory effects,19 and competitive binding of ivermectin with the viral S protein as shown in multiple in silico studies. The latter would inhibit viral binding to ACE-2 receptors suppressing infection. Hemagglutination via viral binding to sialic acid receptors on erythrocytes is a recently proposed pathologic mechanism that would be similarly disrupted. Both host-directed and virus-directed mechanisms have thus been proposed, the clinical mechanism may be multimodal, possibly dependent on disease stage, and a comprehensive review of mechanisms of action is warranted.

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You can’t force people. And you shouldn’t be trying.

Stop The Mandates Or People Die (Denninger)

Better watch this one folks and let it sink in.

“If I don’t show up for my job, as I just explained to you, people die. On Saturday night at 10 p.m. I got a page. I did not want to go to work. Somebody was having a very critical problem, they were dying. I worked until 6 a.m. the next day. If I had not of showed up, there would have been nobody to do my job. These guys can’t show up to their job, and I’m sorry, your jobs are not as important as mine.” There are tens if not hundreds of thousands of people just like him They’re everywhere in the health care system. They have unique skills without which the system does not function, and when you need those skills you need them now, not later. There is no “later”; there is either now or death. Take someone on dialysis. This is not a “robotic procedure”; each patient has specific levels of various drugs and their specific metabolic reactions to them that must be individually managed.

The people who do that job are not replaceable on short notice, if at all. If you need dialysis and do not get it, you die. This is not a “maybe” or “might die” you WILL die with absolute, 100% certainty. Things happen at odd hours of the day and night. Most real medical emergencies are not scheduled — heart attacks, strokes, car wrecks, gunshots and similar. They happen when they happen and either someone is there to respond to it and deal with it or the person in question dies. Those hundreds of thousands of people who are utterly essential to people not dying every single day — hundreds if not thousands who will otherwise die if those employees refuse to show up — and exactly zero of those people can be compelled to work. This is America. It is not the Soviet Union. It is not North Korea.

NOBODY is a slave and EVERYONE has the right to say “**** you” and walk out. EVERYONE. ALL THE TIME. Then there are of course both cops and firefighters. You want someone to put your house out if its on fire, right? What if the firefighters say “**** you” to a jab mandate and quit? Who’s going to put the fire out? Do you even have a wrench to get the hydrant open, say much less the correct fittings and hose? What happens when your child is in that burning house and there is no firefighter to put it out? He or she dies. You cannot arrest and jail someone for quitting their job or refusing a mandate and being fired. All employment is voluntary, no matter how “essential” the position. THERE ARE NO EXCEPTIONS and there is no way to replace the people who do these jobs without which hundreds of people per day WILL DIE.

Therefore you have a choice to make America and you have to make it NOW. You will stand up and stop these mandates. You will do it now. You will do it or every single person who dies as a result of your failure to do so, and the refusal of others to consent, is YOUR responsibility. Not their person who quits — YOURS. THEY are not slaves. THEY cannot be compelled to consent. THEY have NO obligation to put up with your bull****. You’d better get this through your thick ******n skull RIGHT NOW. YOU are why that person who needs dialysis will be dead. YOU are why the person who is in critical trouble in a hospital and there is no perfusionist available right now will die. YOU either stop this madness, right now, by whatever means are necessary, without exception from top to bottom or YOU are responsible for those deaths and those deaths WILL come.

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“While replication-associated mutations generate small changes in the viral genome, recombination may introduce more important modifications, leading to dramatic changes in the phenotype of SARS-CoV-2..”

Molecular Determinants of SARS-CoV-2 Variants (Cell)

Accumulation of genomes with replication-associated random mutations within the same cell has the potential to generate a heterogeneous mix of viral proteins, including spike protein, which brings into question the true diversity of the spike on the surface of individual virions and subsequent tissue-level spread of SARS-CoV-2 and its variants. If a more orderly molecular process to regulate the homogeneous distribution of spike protein variants on individual virions exists, it remains to be identified. Regular RNA sequencing analyses are unable to identify these differences since they can only be captured by ultra-high-resolution single-virion protein sequencing, the technology for which is in its infancy.

The SARS-CoV-2 genomic mutation rate in humans is estimated at 0.8-2.38 x 10-3 nucleotide substitutions per site per year largely based on analysis of sequencing data archived in public repositories. Emerging studies are attempting to confirm this mutation rate using experimental investigations. By comparison, mutations rates for influenza A virus and Middle East respiratory syndrome CoV (MERS-CoV) are 2.3 x 10-3 and 1.12 x 10-3 nucleotide substitutions per site per year, respectively. Human CoVs (HCoV)-OC43 and HCoV-229E have an average mutation rate of 3-6 x 10-4 nucleotide substitutions per site per year. Emerging experimental data suggest that SARS-CoV-2 is capable of mutating and accumulating changes when facing a new cell type, albeit in the absence of immune surveillance in a single-cell-type infection model. A clinical study also reported the rapid evolution of SARS-CoV-2 variants in the presence of antibodies from convalescent plasma therapy. While random errors during replication may induce genetic mutations in SARS-CoV-2, multiple extrinsic factors, such as individual and population-level immunity, play a vital role in the selection of these variants. More research is warranted to fully understand the cellular and molecular drivers of genomic mutation and selection in SARS-CoV-2. As SARS-CoV-2 accumulates new genetic changes, we shall need to reassess the mutation rate to better understand the contribution of replication-associated random mutations and its impact on SARS-CoV-2 transmission and emergence of new variants.

Figure 1 Replication-Associated Generation of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Variants.

While replication-associated mutations generate small changes in the viral genome, recombination may introduce more important modifications, leading to dramatic changes in the phenotype of SARS-CoV-2 (Figure 2). Discontinuous transcription of CoV genomes enables recombination in a cell coinfected with more than one CoV species or variant via ‘strand switching’ by the viral RdRp (Figure 2A). This process leads to the production of chimeric subgenomic RNA and proteins. Chimeric proteins may have consequences for the fate of infected cells and for cellular and tissue tropism of progeny virions. As technology evolves, we might be able to track the spread of individual virions, along with deciphering the heterogeneity of their composition.

Figure 2 Recombination-Induced Variants.

Read more …

Dr. Robert Malone and Peter Navarro.

Biden Team’s Misguided And Deadly Covid-19 Vaccine Strategy (WT)

The Biden administration’s strategy to universally vaccinate in the middle of the pandemic is bad science and badly needs a reboot. This strategy will likely prolong the most dangerous phase of the worst pandemic since 1918 and almost assuredly cause more harm than good – even as it undermines faith in the entire public health system. Four flawed assumptions drive the Biden strategy. The first is that universal vaccination can eradicate the virus and secure economic recovery by achieving herd immunity throughout the country (and the world). However, the virus is now so deeply embedded in the world population that, unlike polio and smallpox, eradication is unachievable. SARS-CoV-2 and its myriad mutations will likely continually circulate, much like the common cold and influenza.

The second assumption is that the vaccines are (near) perfectly effective. However, our currently available vaccines are quite “leaky.” While good at preventing severe disease and death, they only reduce, not eliminate, the risk of infection, replication, and transmission. As a slide deck from the Centers for Disease Control has revealed, even 100% acceptance of the current leaky vaccines combined with strict mask compliance will not stop the highly contagious Delta variant from spreading. The third assumption is that the vaccines are safe. Yet scientists, physicians, and public health officials now recognize risks that are rare but by no means trivial. Known side effects include serious cardiac and thrombotic conditions, menstrual cycle disruptions, Bell’s Palsy, Guillain Barre syndrome, and anaphylaxis.

Unknown side effects which virologists fear may emerge include existential reproductive risks, additional autoimmune conditions, and various forms of disease enhancement, i.e., the vaccines can make people more vulnerable to reinfection by SARS-CoV-2 or reactivation of latent viral infections and associated diseases such as shingles. With good reason, the FDA has yet to approve the vaccines now administered under Emergency Use Authorization. The failure of the fourth “durability” assumption is the most alarming and perplexing. It now appears our current vaccines are likely to offer a mere 180-day window of protection – a decided lack of durability underscored by scientific evidence from Israel and confirmed by Pfizer, the Department of Health and Human Services, and other countries.

Here, we are already being warned of the need for universal “booster” shots at six-month intervals for the foreseeable future. The obvious broader point that militates for individual vaccine choice is that repeated vaccinations, each with a small risk, can add up to a big risk. It’s an arms race with the virus.

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Still not sure what they’re mad about, other than lockdowns.

100s Of Doctors Sign Open Letter: Need Debate On ‘Flawed Covid Guesses’ (Exp.)

A hundred and thirty three doctors, nurses, psychiatrists paramedics and midwives signed the letter released today which states that despite a “complete lack of widespread approval among health professionals,” of the pandemic policies, “no attempt” has been made to measure the harms of lockdown policies. The letter, also addressed to the Health Secretary and First Ministers for Scotland, Wales and Northern Ireland states: “You have failed to engage in dialogue and show no signs of doing so. You have removed from people fundamental rights and altered the fabric of society with little debate in Parliament.” The signatories, from a broad range of specialities, came forward despite the risk of doing so to both their jobs and reputations.

Founding signatory Dr Ros Jones, a retired paediatric consultant said: “We wrote the letter as a group of healthcare professionals, connected only by our deep concern and shared commitment to “first do no harm.” We can no longer stand by in silence. We are not the first group of medically and scientifically qualified professionals to write in such terms to the Government. In March, 22 eminent scientists publicly called for drastic policy change. We sincerely hope we will be the last who feel the need to write such a letter.” Dr Alan Mordue, another founding signatory said: “To move forward now our governments urgently need to facilitate a wider and open debate within the medical and scientific community, for the short term as we lift restrictions, and the longer term to improve how we manage winter respiratory viruses and pandemics in the future.”

Concerns voiced in the letter include accusations that no Minister responsible for policy “has engaged in an open and full discussion of alternative ways of managing the pandemic,” despite being aware of other medical and scientific viewpoints. It adds the pandemic response policies have caused “significant, permanent and unnecessary harm” to the UK and “must never be repeated.” The letter focuses on 10 areas where the UK’s approach to COVID failed. It argues the nature of the covid threat has been exaggerated, it claims the use of behavioural science to generate fear was “inappropriate and unethical” and it argues the role of asymptomatic spread has been overplayed and used to promote public compliance with restrictions.

Finally it states that restrictions have been imposed with an overreliance on modelling data whilst ignoring real world data. The signatories called for a “sea change within the Government “which must now pay proper attention to those esteemed experts outside its inner circle who are sounding these alarms.”

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New normal. I see videos every day from Australia that make me want to vomit.

Rescue Dogs Shot Dead By NSW Council Due To Covid-19 Restrictions (SMH)

Several impounded dogs due to be rescued by a shelter have instead been shot dead by a rural council in NSW under its interpretation of COVID-19 restrictions, alarming animal activists and prompting a government probe. Bourke Shire Council, in the state’s north-west, killed the dogs to prevent volunteers at a Cobar-based animal shelter from travelling to pick up the animals last week, according to council’s watchdog, the Office of Local Government. “OLG has been informed that the council decided to take this course of action to protect its employees and community, including vulnerable Aboriginal populations, from the risk of COVID-19 transmission,” a spokesman from the government agency said.

The spokesman said the agency was examining the circumstances of the incident to find out whether companion animal and cruelty prevention laws had been broken. The Herald attempted to contact the council administration multiple times, but received no response, and a member of Rural Outback Respite/Rescue – the shelter that was supposed to receive the dogs – declined to comment. A source who is familiar with the arrangement said the shelter volunteers are distressed and had COVID-safe measures in place to handle the dogs, one of which was a new mother. According to NSW Health, there have been no recent locally acquired COVID-19 cases in Cobar, although fragments of the virus have been found in the area’s sewerage system.

The Office of Local Government Minister Shelley Hancock, who has previously faced questions in Parliament over the shooting of animals in council pounds, did not comment. However, animal liberation campaigner Lisa Ryan called for an urgent investigation. “We are deeply distressed and completely appalled by this callous dog shooting and we totally reject council’s unacceptable justifications that this killing was apparently undertaken as part of a COVID- safe plan,” Ms Ryan, Animal Liberation’s regional campaign manager, said.

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“It would be better to die under the Taliban’s bullet” than face the crowds again..”

Afghan Staff At US Embassy Losing Faith In Evacuation Efforts (NBC)

Local staff members at the U.S. Embassy in Kabul are “deeply disheartened” by U.S. evacuation efforts and have expressed a sense of betrayal and distrust in the U.S. government, according to a State Department diplomatic cable obtained by NBC News. The cable, which was sent Saturday, said memos were sent Wednesday inviting Afghan staff members at the embassy to head to Hamid Karzai International Airport in Kabul. It told them to take food and to prepare for difficult conditions. “However, no one anticipated the brutal experience that occurred,” the cable said.

Staffers reported being jostled, hit, spat on and cursed at by Taliban fighters at checkpoints near the airport, it said, adding that criminals were taking advantage of the chaos while the U.S. military tried to maintain order “in an extremely physical situation.” Some staff members reported that they were almost separated from their children, while others collapsed in a crush of people and had to be taken to hospitals with injuries, the cable said. Others said they had collapsed on the road because of heat exhaustion, it said. “It would be better to die under the Taliban’s bullet” than face the crowds again, a staff member was quoted as saying in the cable.

“Happy to die here, but with dignity and pride,” another said, while a third accused the U.S. of prioritizing Afghan government elites with contacts in the U.S., who already had the correct paperwork and other ways to flee the country. A local embassy staff member reported that his home had been tagged with spray paint — a tactic the Taliban have used in the past to identify homes’ occupants for further questioning, the cable said, adding that the family had been forced to flee their home but was unable to get to the airport. Others shared concerns about conditions in Qatar, where many refugees have been flown before they make their way to other locations.

The U.S. began evacuating its citizens, diplomatic staff members and Afghans who aided its mission in the country last week after the Taliban seized control of much of Afghanistan before they finally walked into Kabul last Sunday without firing a shot. A State Department spokesperson said the U.S. has a “special commitment” to local embassy staff members who “have suffered hardship, pain and loss because of their dedication to working with us to build a better future for all Afghans.”

Read more …

… But They’re Also Not Looking For Her Very Hard

White House Announces They’ve Lost Kamala Harris (BBee)

In an interview with Morning Joe, White House communications director Kate Bedingfield revealed they have lost Kamala Harris and have no idea where she’s gone, although she admitted nobody is really looking for her all that hard. “Yeah, I dunno. She’s somewhere, I guess. I mean, she didn’t just disappear,” said Bedingfield. “We have some people looking for her I think, but we’re not too worried, honestly. I’m sure she’ll turn up sooner or later.” “Wait, wait, wait,” said the show’s host. “You mean to tell me that in this time of crisis, you have literally no idea where the Vice President of the United States is?”

“Well, it sounds bad when you put it that way,” replied the Communications Director. “I don’t really see how this is a big deal. It’s been kind of nice and quiet around here since she left… we’re not even quite sure what she does, anyway,” she said with a shrug. Anonymous sources have suggested Kamala may be somewhere around Camp David, as locals reported the sound of cackling through the night.

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  • #85058

    Didn’t Dr. McCullough say he welcomed approval so real tests could be done on the “vaccine”? They could actually take it apart and see what’s in it?

    The ideal product produces addiction- something you don’t just want, but that you need.
    Withholding is one of the best manipulative devices of all.

    John Day

    Thanks to All-Y’all again today. My heart is happy to see your writings. Picture of me on the blog is not the one of me bending over and picking the squash.
    That one was all butt, not flattering at all.
    This one makes me look buff and sexy holding a fresh vegetable in the squash & banana patch

    The “more fortunate” countries of the world made the kind of deal with Pfizer last fall, that you or I might make with a mortgage lender, or when taking out a home-equity loan. The superior party bears no risk, and actually gains even more if the lesser party defaults. No way out, except to pay up.
    Pfizer had good reason to exact such iron-clad contracts, which held Pfizer blameless in any circumstance which might arise. It’s good-business, of course, but the risks for antibody dependent enhancement (of viral pathogenicity) were well known, and no coronavirus vaccine studied had been successful in 20 years of trying.
    The vaccinated animals made antibodies, but died at higher rates than the unvaccinated animals when challenged with viral infection.
    Antibodies “against” a virus can turn out to be “for” the virus, to help it be more infectious.
    That effect takes time to develop, like half a year to get started, in general.
    There is evidence that is happening with vaccines against the original “alpha”-COVID spike protein now helping the Indian-originated delta-COVID have enhanced infectivity in vaccinated people.
    That is just getting started, though, because it’s kind of accidental that delta-COVID can do a bit of this. Delta-COVID evolved in India with about 4% population vaccination, so it was just trying to spread effectively in a population. It did not have to dodge vaccine-created antibodies on the path to that success.
    Now, in much of the world, like where we live, a majority of susceptible people have blocking-and-enhancing antibodies to alpha-COVID spike protein, due to vaccination. The viral mutations of resistance to blocking antibodies will be rewarded with more viral success in spread, but there is now a new option. Viral mutation to get more TURBO-BOOST out of the enhancing antibodies opens the door to new viral strains that will be more infectious to the vaccinated than to the unvaccinated.
    This environmental niche has been created among spike-protein-vaccinated human hosts.
    I suspect that mutant COVID variants yet-unnamed are already filling it.
    Stay tuned, especially to Israel.

    John Day

    I’ll break these up. They wouldn’t post together:

    A scientific paper from Nature, last October, gives clear historical context regarding this common and devastating and difficult to avoid vaccination side effect.
    Look, they got this problem when they tried to make vaccines for SARS-Co-V and MERS, the close cousins of our current COVID family.
    ​ ​In this Perspective, we summarize examples of vaccine-associated disease enhancement in the history of developing vaccines against respiratory syncytial virus, dengue virus, SARS-CoV and Middle East respiratory syndrome coronavirus, which highlight the importance of a robust safety and efficacy profile, and present recommendations for preclinical and clinical evaluation of COVID-19 vaccine candidates as well as for vaccine design and optimization.

    ​ Here is a specific mechanism of vaccine-antibodies to alpha-COVID spike protein enhancing the ability of delta-COVID to enter human cells, once the spike protein anchors to the cell.​ This is demonstrated to predominate in effet over the blocking antibodies, since delta mutated and they lost effectiveness against it.
    Infection-enhancing anti-SARS-CoV-2 antibodies recognize both the original Wuhan/D614G strain and Delta variants. A potential risk for mass vaccination?
    ​ ​Using molecular modeling approaches, we show that enhancing antibodies have a higher affinity for Delta variants than for Wuhan/D614G NTDs. We show that enhancing antibodies reinforce the binding of the spike trimer to the host cell membrane by clamping the NTD to lipid raft microdomains. This stabilizing mechanism may facilitate the conformational change that induces the demasking of the receptor binding domain. As the NTD is also targeted by neutralizing antibodies, our data suggest that the balance between neutralizing and facilitating antibodies in vaccinated individuals is in favor of neutralization for the original Wuhan/D614G strain. However, in the case of the Delta variant, neutralizing antibodies have a decreased affinity for the spike protein, whereas facilitating antibodies display a strikingly increased affinity.

    John Day

    Pfizer coerced deals upon countries that desired to obtain it’s COVID-19 vaccines last year, which broke laws of those countries, could not be revoked under any conditions or in light of new information or treatments (ivermectin, deadly side effects), and in some cases gave Pfizer ownership of things like military bases, should the country default. Thanks Luc. It was a seller’s market. Israel got a deal.
    ​ In history’s largest medical experiment with “vaccines” that have not been approved for use in humans, it is the buyers’ responsibility to defend Pfizer for causing harm, leaked documents showed. Pfizer has escaped all liability and is indemnified, arguing that side effects and the long-term effects of the injections are unknown – to the company as well. Pfizer thus admits that an insufficiently tested product is being pushed in literally billions of doses on the world market.
    This means that all responsibility for costs, healthcare, etc. due to vaccine damage – no matter how large and onerous – is passed on to the taxpayers in the countries that have signed the agreements. Since the agreements put each country’s own laws out of play, they have all been signed at government level.

    Bombshell leak: Countries that buy Pfizer’s vaccine undertake to break the law

    (Ram it through quick!) British Medical Journal: Covid-19: FDA set to grant full approval to Pfizer vaccine without public discussion of data
    ​ ​Last year the FDA said it was “committed to use an advisory committee composed of independent experts to ensure deliberations about authorisation or licensure are transparent for the public.”1 But in a statement, the FDA told The BMJ that it did not believe a meeting was necessary ahead of the expected granting of full approval.

    ​ People have not been able to get doctors to prescribe ivermectin for COVID treatment and prevention, so they have bought veterinary ivermectin to use, mostly the horse-paste, but there are also some horse pills. A horse weighs about 10 times as much as a human, so people who take a horse pill, at 10X the human dose are getting nausea, vomiting, diarrhea and dizziness, but that’s all. No deaths, and the one “hospitalization” in Mississippi, does not appear to be confirmed. Take the right dose. If you can’t do math, get help from a farm-boy who can. These horse products are used on goats, rabbits, farmers and farmers children, at the correct scaling doses. Ask a farmer with critters.​ FDA resorts to shouting and public shaming, because it’s hard to fear safer-than-Tylenol ivermectin.
    The FDA Is Begging You Not to Take Horse Dewormer for Covid-19
    “You are not a horse. You are not a cow,” the Food and Drug Administration said about using the drug that hosts on Fox News have been pushing

    The FDA Is Begging You Not to Take Horse Dewormer for Covid-19

    ​American Journal of Therapeutics:
    Moderate-certainty evidence finds that large reductions in COVID-19 deaths are possible using ivermectin. Using ivermectin early in the clinical course may reduce numbers progressing to severe disease. The apparent safety and low cost suggest that ivermectin is likely to have a significant impact on the SARS-CoV-2 pandemic globally.


    Comment from Denninger, someone had the stomach to read the FDA papers, and it looks like an extension of the EUA. Another bluff?

    Doc Robinson

    Some of the points myade by a senior editor of the British Medical Journal BMJ.
    (Thanks to John Day for the link.)

    Does the FDA think these data justify the first full approval of a covid-19 vaccine?
    August 23, 2021

    The elephant named “waning immunity”
    …“Waning immunity” is a known problem for influenza vaccines, with some studies showing near zero effectiveness after just three months, meaning a vaccine taken early may ultimately provide no protection by the time “flu season” arrives some months later. If vaccine efficacy wanes over time, the crucial question becomes what level of effectiveness will the vaccine provide when a person is actually exposed to the virus? Unlike covid vaccines, influenza vaccine performance has always been judged over a full season, not a couple months.
    And so the recent reports from Israel’s Ministry of Health caught my eye. In early July, they reported that efficacy against infection and symptomatic disease “fell to 64%.” By late July it had fallen to 39% where Delta is the dominant strain. This is very low. For context, the FDA’s expectation is of “at least 50%” efficacy for any approvable vaccine.

    Delta may not be responsible
    Enter Pfizer’s preprint. As an RCT reporting “up to six months of follow-up,” it is notable that evidence of waning immunity was already visible in the data by the 13 March 2021 data cut-off… And it’s hard to imagine how the Delta variant could play a real role here, for 77% of trial participants were from the United States, where Delta was not established until months after data cut-off.
    Waning efficacy has the potential to be far more than a minor inconvenience; it can dramatically change the risk-benefit calculus.

    The “six month” preprint based on the 7% of trial participants who remained blinded at six months
    Despite the reference to “six month safety and efficacy” in the preprint’s title, the paper only reports on vaccine efficacy “up to six months,” but not from six months. This is not semantics, as it turns out only 7% of trial participants actually reached six months of blinded follow-up (“8% of BNT162b2 recipients and 6% of placebo recipients had ≥6 months follow-up post-dose 2.”) So despite this preprint appearing a year after the trial began, it provides no data on vaccine efficacy past six months, which is the period Israel says vaccine efficacy has dropped to 39%.
    It is hard to imagine that the <10% of trial participants who remained blinded at six months (which presumably further dwindled after 13 March 2021) could constitute a reliable or valid sample to produce further findings.

    Severe disease
    And on preventing death from covid-19, there are too few data to draw conclusions—a total of three covid-19 related deaths (one on vaccine, two on placebo). There were 29 total deaths during blinded follow-up (15 in the vaccine arm; 14 in placebo).
    The crucial question, however, is whether the waning efficacy seen in the primary endpoint data also applies to the vaccine’s efficacy against severe disease. Unfortunately, Pfizer’s new preprint does not report the results in a way that allows for evaluating this question.

    Approval imminent without data transparency, or even an advisory committee meeting?
    …But here we are, with FDA reportedly on the verge of granting a marketing license 13 months into the still ongoing, two year pivotal trial, with no reported data past 13 March 2021, unclear efficacy after six months due to unblinding, evidence of waning protection irrespective of the Delta variant, and limited reporting of safety data. (The preprint reports “decreased appetite, lethargy, asthenia, malaise, night sweats, and hyperhidrosis were new adverse events attributable to BNT162b2 not previously identified in earlier reports,” but provides no data tables showing the frequency of these, or other, adverse events.)
    It’s not helping matters that FDA now says it won’t convene its advisory committee to discuss the data ahead of approving Pfizer’s vaccine. (Last August, to address vaccine hesitancy, the agency had “committed to use an advisory committee composed of independent experts to ensure deliberations about authorization or licensure are transparent for the public.”)

    Does the FDA think these data justify the first full approval of a covid-19 vaccine?


    Didn’t Dr. McCullough say he welcomed approval so real tests could be done on the “vaccine”? They could actually take it apart and see what’s in it?

    He thought there would be testing. There won’t be. Also not after the approval.



    I saw that as well, and from what I gathered, the “approval” appears to be an extension of the EUA to include a generic version (biologic) of the Pfizer vaccine. Page 2 and Page 12:

    So yeah, a huge bluff if I’m reading this correctly.

    Doc Robinson

    “…it looks like an extension of the EUA. Another bluff?”

    It looks like the FDA approved the BioNTech brand (identical product to the Pfizer shots, and the Pfizer shots can substitute for the approved brand, the FDA says), while the FDA is keeping the Pfizer shots under the EUA (my guess is to allow younger children to use it with an EUA, or quicker rollout of booster shots, instead of first requiring further studies for the licensed brand).

    On August 23, 2021, FDA approved the biologics license application (BLA) submitted by BioNTech Manufacturing GmbH for COMIRNATY (COVID-19 Vaccine, mRNA) for active immunization to prevent COVID-19 caused by SARS-CoV-2 in individuals 16 years of age and older…

    …the EUA will remain in place for the Pfizer-BioNTech COVID-19 vaccine for the previously-authorized indication and uses, and to authorize use of COMIRNATY (COVID-19 Vaccine, mRNA) under this EUA for certain uses that are not included in the approved BLA…

    COMIRNATY (COVID-19 Vaccine, mRNA) is the same formulation as the PfizerBioNTech COVID-19 Vaccine and can be used interchangeably with the Pfizer-BioNTech COVID-19 Vaccine to provide the COVID-19 vaccination series…


    Thanks, ct and Doc. I can read cogent technical documents all day, but stuff that is designed to obfuscate doesn’t hold my attention.

    Doc Robinson

    From the Pulitzer-prize winning site ProPublica (not quite an “anti-vaxxer” source of misinformation):

    The CDC Only Tracks a Fraction of Breakthrough COVID-19 Infections, Even as Cases Surge

    Meggan Ingram was fully vaccinated when she tested positive for COVID-19 early this month. The 37-year-old’s fever had spiked to 103 and her breath was coming in ragged bursts when an ambulance rushed her to an emergency room in Pasco, Washington, on Aug. 10. For three hours she was given oxygen and intravenous steroids, but she was ultimately sent home without being admitted.

    Seven people in her house have now tested positive. Five were fully vaccinated and two of the children are too young to get a vaccine…

    “It’s like saying we don’t count,” said Ingram after learning of the CDC’s policy change. COVID-19 roared through her household, yet it is unlikely any of those cases will show up in federal data because no one died or was admitted to a hospital.


    “Local staff members at the U.S. Embassy in Kabul are “deeply disheartened” by U.S. evacuation efforts and have expressed a sense of betrayal and distrust in the U.S. government…”

    Hahaha, did they run out of Red, White and Blue Kool Aid ? Betrayal by the US Regime? Distrust of the US Regime War criminals… it took them fearing their own asses to realize the US Regime is untrustworthy. Illegally invading another Nation that had nothing to do with 9/11, but was invaded because of 9/11- I hope they really get to know the Taliban now.

    “If they ban you from their restaurants…”
    Yep it’s happening here in Wa State now. Got reports last night that restaurants in Bellingham and Seattle are now asking for vax cards to enter… funny how a restaurant owner I know was vaxd and got covid.

    So if you are vaccinated and then get covid, do they take your vaccine card away?


    The reason I’m reading it as a generic version is due to the fact I was on a biologic for humalog and lantus insulins while living in MD. A biologic license allows other companies to produce the exact manufacturing techniques as the original instead of replacing one of the ingredients that would preclude a copyright violation. But Doc could be correct in their interpretation of the document, and that’s my hedge.

    But at this point, as another Denninger commenter noted, what difference would it really make? If da TV says it’s full approval, then it’s full approval to the masses.


    “Copyright” violation should be “patent” violation.



    Losing taste and smell is just something I would like to avoid if at all possible. Never mind all of the other long haul symptoms. So, I will take precautions to avoid those negative outcomes.

    Do you think the millions of dead murdered by the US Regimes Illegal wars miss not being able to taste and smell? Are those illegal wars and crimes against humanity committed by the Government you look to for your personal protection mandated and justified in your confused hypocritical mind?

    Have you filed a complaint against the US Govt for murdering healthy citizens across the globe ?
    Have you filed a complaint against Fauci and Gates funding biological weapons research at Wuhan?
    So you support Fort Detrick and the US Biological Weapons Research and the millions of dollars spent creating Biological weapons by the US Regime?

    Does your confused mind tell you those Wars and Murders are necessary and justified…the same confused mind that believes that masks that don’t protect you will protect you? Your same confused mind that thinks the Vaccine will prevent you from getting the covid engineered bio weapon which actually does not prevent you from infection?


    Interesting name for the newly-approved COVID “vaccine”. Names are of significance, I think; and that’s a curious one. Variations of same, too: see “ISIS, ISIL, Islamic State; Al Quaeda and its “variants”, and the many, many other re-brandings in our enlightened, and super high-tech™ world.

    “Confusion” reigns (by design, I’d say).

    On a better note, some flowers unexpectedly bloomed in my tiny garden this weekend. Victory..

    Doc Robinson

    “A Biologics License Application, or BLA, is FDA’s standard “full approval” mechanism for biological products, including therapeutics and vaccines.”

    What’s the Difference Between Vaccine Approval (BLA) and Authorization (EUA)?

    What’s the Difference Between Vaccine Approval (BLA) and Authorization (EUA)?

    Mr. House

    Well the results are in: I have two types of antibodies! Double the fun. Anyways Karl D said don’t get an antibody test until two weeks after you stop showing symptoms. The nurse i spoke with at CVS confirmed this. So a week after i was showing for them, thats good. Negative test for covid and positive on the antibodies. If i could taste beer i’d go out and celebrate ;).


    I found this piece when looking for more info on Malcolm Kyenune:

    Which Side Are You On? The Answer is Clear for Today’s Useful Idiots for the Right

    Not essential at all; but notable for its nastiness toward anyone suggesting solidarity toward others that aren’t just like you, for a Greater Good (a term that they’re working hard
    to debase, as well). Reads like one of Our -IA friends’ work to me, actually..

    The light of Fall is beginning to show even though it’s still August, and I like that (no hidden meaning there, I just like that somehow-poignant slant best). Taking meaning where I can find it.


    I stand corrected. Thanks Doc.


    Re.: Central retinal vein occlusion
    Doc feels that mine is the hardening of the veins due to old age.
    No solution to fix.
    Get injections once per month and laser to maybe help from getting worst.
    The doc said, had one patient due to vaccine.


    Does the “Delta Strain” exist? How could one know?

    Does a COVID hysteria exist? To that I can safely say “yes”, though I *still know of no one* who
    become seriously ill or died, as a result of COVID. One anecdote.


    Zinc does seem to be better absorbed when taken with green tea, IME. I’ve been using the Jarrow
    ‘Zinc Balance’ because it has a little bit of copper in it.

    Doc Robinson

    TDub: “We are continuously told that it is a “pandemic of the unvaccinated” with scary statistics like 99% of those in the hospital are unvaxxed. Does anyone have a source for that data?”

    New York Magazine (clearly not an “anti-vaxxer source of misinformation”) examined those numbers and says they are distorted (“a closer look at the data reveals that some of the public-health communication may be overstating the vaccine effect on transmission and understating the scale and risk of breakthrough infections.” )

    “The message that breakthrough cases are exceedingly rare and that you don’t have to worry about them if you’re vaccinated — that this is only an epidemic of the unvaccinated — that message is falling flat,” Harvard epidemiologist Michael Mina told me…

    On Wednesday, a large pre-print study published by the Mayo clinic suggested the [vaccine] efficacy against infection had fallen as far as 42 percent.

    The breakthrough problem is much more concerning than what our public officials have transmitted,” Topol continued. “We have no good tracking. But every indicator I have suggests that there’s a lot more under the radar than is being told to the public so far, which is unfortunate.” The result, he said, was a widening gap between the messaging from public-health authorities and the meaning of the data emerging in real time. “I think the problem we have is people — whether it’s the CDC or the people that are doing the briefings — their big concern is, they just want to get vaccinations up. And they don’t want to punch any holes in the story about vaccines. But we can handle the truth. And that’s what we should be getting.”

    The central distortion reflected in the Kaiser report — and echoed by communicators elsewhere, including in the Times — is the result of a basic error of comparison, one that should have been obvious to anyone familiar with the shape of the pandemic. Almost all of these calculations about the share of breakthrough cases have been made using year-to-date 2021 data, which include several months before mass vaccination (when by definition vanishingly few breakthrough cases could have occurred) during which time the vast majority of the year’s total cases and deaths took place (during the winter surge).This is a corollary to the reassuring principle you might’ve heard, over the last few weeks, that as vaccination levels grow we would expect the percentage of vaccinated cases will, too — the implication being that we shouldn’t worry too much over panicked headlines about the relative share of vaccinated cases in a state or ICU but instead focus on the absolute number of those cases in making a judgment about vaccine protection across a population. This is true. But it also means that when vaccination levels were very low, there were inevitably very few breakthrough cases, too. That means that to calculate a prevalence ratio for cases or deaths using the full year’s data requires you to effectively divide a numerator of four months of data by a denominator of seven months of data. And because those first few brutal months of the year were exceptional ones that do not reflect anything like the present state of vaccination or the disease, they throw off the ratios even further. Two-thirds of 2021 cases and 80 percent of deaths came before April 1, when only 15 percent of the country was fully vaccinated, which means calculating year-to-date ratios means possibly underestimating the prevalence of breakthrough cases by a factor of three and breakthrough deaths by a factor of five. And if the ratios are calculated using data sets that end before the Delta surge, as many have been, that adds an additional distortion, since both breakthrough cases and severe illness among the vaccinated appear to be significantly more common with this variant than with previous ones.

    Unfortunately, more accurate month-to-month data is hard to assemble — because the CDC stopped tracking most breakthrough cases in early May, before the Delta wave had begun, and the states maintaining their own databases often update them irregularly and, in some cases, according to idiosyncratic logic..

    Don’t Panic, But Breakthrough Cases May Be a Bigger Problem Than You’ve Been Told Current public-health messaging may understate the scale and risk.


    > Negative test for covid and positive on the antibodies. <



    @Doc Robinson – thanks for that article. “Their big concern is, they just want to get vaccinations up. And they don’t want to punch any holes in the story about vaccines.

    If NY Magazine was able to review those numbers, does that mean they exist somewhere for the rest of us to see? A few similar comparisons from Israel have been shown on TAE before, would be nice to see the hard numbers that support the ‘pandemic in the unvaxxinated claim”


    Just finished watching the Dellingpole/Miller interview: ding ding ding ding ding! Miller even mentions having just finished “That Hideous Strength”. I’ll have to find his donation page to help his lawsuit.
    Git yer money off to the folks you love before it’s worthless!


    > ‘Don’t Panic, But Breakthrough Cases May Be a Bigger Problem Than You’ve Been Told’ <

    Yes, more interesting messaging: “Don’t panic/please panic!!!”

    And over at NC the “vaccine” approval didn’t seem to merit even a post. Odd..
    also, the few worthy commenters there are no longer appearing; not sure if
    they’re being “moderated”, or there other reasons.

    Looking forward to the days- maybe soon to come- when “messaging” will be a very bad word.


    information and power asymmetry increases..

    hey wheres cosco

    Polder Dweller

    I just watched Catherine Austin-Fitts talking to Del Bigtree. A lot of similar information as in the Planet Lockdown video with her that I posted yesterday. I recommend you watch that, although this is quite good, too.

    She explains about how everything is being set up for a move to a central bank digital currency (The Grim Reset) and the vaccine passports are an essential part of that which will allow full monitoring (and control) of everything you do and hence a social credit scheme. The lockdowns and the riots of last year were to trash small businesses and hand their real estate to the likes of Blackrock etc. The “vaccines” are to reduce life expectancy and hence solve the pension crisis, but you all already knew all that.

    <iframe class=”rumble” width=”640″ height=”360″ src=”; frameborder=”0″ allowfullscreen></iframe>


    Simpler: They want us to know, and disseminate.

    stuff like that


    John Day: nice photo with the Squash. Looks like my Mom’s plot in the Central Valley circa 1975 or so.
    Would’ve said said so on your blog but can’t seem to comment there. Lovely to see life coming out of
    the ground.


    “Pandemic of the unvaccinated” is a phrase I’ve been reading a lot lately in MSM and official pronouncements.
    Something seems off.

    Consider the following options:
    1) “Pandemic among the unvaccinated”
    2) “Pandemic in the unvaccinated”
    3) “Pandemic of the unvaccinated”

    What solution(s) to the problem “pandemic” are implicitly suggested by each?
    Why use the third?


    Jonathan Richman wrote and sang ‘Monologue About Bermuda’ (hope I got the exact title right).
    It’s worth hearing, I think. He doesn’t use a compyooter. Kudos, JR!


    Because the unvaccinated are the disease, of course. (grrrr) >:(


    This part of the letter struck me as very strange though, and of course I know it’s designed to confuse:

    “Conditions Related to Printed Matter, Advertising, and Promotion

    X. All descriptive printed matter, advertising, and promotional material, relating to the
    use of the Pfizer-BioNTech COVID‑19 Vaccine shall be consistent with the
    authorized labeling, as well as the terms set forth in this EUA, and meet the
    requirements set forth in section 502(a) and (n) of the FD&C Act and FDA
    implementing regulations.

    Y. All descriptive printed matter, advertising, and promotional material relating to the
    use of the Pfizer-BioNTech COVID‑19 Vaccine clearly and conspicuously shall state

    • This product has not been approved or licensed by FDA, but has been
    authorized for emergency use by FDA, under an EUA to prevent Coronavirus
    Disease 2019 (COVID-19) for use in individuals 12 years of age and older; and

    • The emergency use of this product is only authorized for the duration of the
    declaration that circumstances exist justifying the authorization of emergency
    use of the medical product under Section 564(b)(1) of the FD&C Act unless the
    declaration is terminated or authorization revoked sooner.

    Seems strange they would include those qualifiers.


    Hi Raul, A few days ago, I swear we saw a wonderful video about the vaccinations, featuring a young woman who was arguing with herself about why one should (should not) get a vaccination. She took on both the role of the person pushing the vaccines and the person asking perfectly reasonable questions about why it would even be advised, since it doesn’t work. When I go back to find that video (I believe it was originally from Tik Tok), I cannot find it. Could someone please post it again? I want to share it with others who feel as I do, that there is no logic to the argument that one should get the shot. Thank you for considering this request!


    St Vincent’s hospital in Dublin is admitting a “worrying” number of double-vaccinated patients for treatment for Covid-19, emergency department head Professor John Ryan has said.


    The authoritarian corporate state is fully in place in the West. The basic problem is that criminal taking of wealth only works as long as the crooks are allowed to leave devastation in their wake. Kabul fell because the Afghans fought back against the Imperialist imposed corrupt government.

    The FDA approval of the marketing of “Comimaty” vaccine without a public hearing was done to avoid discussion of the known risks, unknown long-term risks, the vaccine’s failure to prevent transmission of the virus, and fading efficacy just months after injection. That this for-profit vaccine is the sole US governmental response to the Coronavirus Pandemic plus the rising death toll from the Delta Variant show utter incompetence. Only the restoration of democracy, good governance and the rule of law will avoid chaos and preserve civilization.

    When the internet and TAE are silenced, recognize that this is a sign of the final death throes of global predatory capitalism.


    > recognize that this is a sign of the final death throes of global predatory capitalism. <


    sure, sure..

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