Covid Safety Quotes

These are not ordinary times where we play politics and juggle with the safety of the society. These are the times that demand prompt decisions and utter responsibility towards not just the self but our kind – the humankind.

Every right comes with responsibility. If you choose to go to work, church, gym, school, mall, club, park, tavern , to visit your friends, family or to go and buy alcohol, because it is your right. You also should know you are responsible for your own safety and other people safety. Whatever the outcome is. You should be held accountable for your actions.

During the COVID-19 pandemic, I would rather take too many safety precautions than too few.

Regarding health and safety issues, never trust the government.

If I were a doctor or nurse and I showed up to the hospital and found they had no sterile personal protective equipment (PPE), I would go to the staff room and wait until the health and safety issues were resolved.

People have been talking and warning other people about corona virus everyday, but some people don’t want to listen. Now corona virus will be speaking for itself. You will see the results on what it can do. I hope people will listen then and I hope it won’t be too late for them . Always remember. If your ear can’t hear it, then your body will hear it. If you can’t listen , then you will feel it.

High-quality and transparent data, clearly documented, timely rendered, and publicly available are the sine qua non of competent public health management. During a pandemic, reliable and comprehensive data are critical for determining the behavior of the pathogen, identifying vulnerable populations, rapidly measuring the effectiveness of interventions, mobilizing the medical community around cutting-edge disease management, and inspiring cooperation from the public. The shockingly low quality of virtually all relevant data pertinent to COVID-19, and the quackery, the obfuscation, the cherrypicking and blatant perversion would have scandalized, offended, and humiliated every prior generation of American public health officials. Too often, Dr. Fauci was at the center of these systemic deceptions. The “mistakes” were always in the same direction—inflating the risks of coronavirus and the safety and efficacy of vaccines in

During the early stages of the Covid-19 lockdown, prominent newspaper columnists defended their right to have someone clean their homes, even at significant risk to their health, on dubiously feminist grounds. Their argument was that without outsourcing domestic work it would be women who had to do the bulk of it. We might wonder if their cleaners were not also women. When the journalist Owen Jones criticised the cavalier attitude that employers of cleaners were taking to workplace safety, he was accused of sexism. His accusers claimed to be fighting the idea that women have some natural duty or propensity to cleaning but the upshot of their argument was that it is fine for some other – i.e. poorer, usually migrant – women to pick up after them. Escaping the confines of the domestic feminine was their individual prerogative, not a shared horizon for all women.

MALONE: Well, on the treatment front, the Merck and Pfizer drugs are really fairly toxic and not particularly effective. That will come out publicly. The deadly nature of remdesivir will become more and more clear. The safety and effectiveness of the early treatment strategies that Drs. Tony Urso, Ryan Cole, and Peter McCullough and everybody have been promoting will become clearer. So it will become clearer that there were unnecessary deaths due to suppression of early treatment. As for the vaccines, because the Pfizer data package will continue to roll out and continue to be nitpicked, you’ll learn more and more about the various malfeasance that’s occurred. There will be increasing awareness of the reproductive risks and the coagulopathy, stroke, blood clotting, autoimmune disease, and this kind of chronic malaise of the post-vaccinated. Those risks will be known to a greater extent. I think that there’ll be increased awareness of the damage to immune systems and the dangerous consequences of that.

We could have dramatically reduced COVID fatalities and hospitalizations using early treatment protocols and repurposed drugs including ivermectin and hydroxychloroquine and many, many others.” Dr. McCullough has treated some 2,000 COVID patients with these therapies. McCullough points out that hundreds of peer-reviewed studies now show that early treatment could have averted some 80 percent of deaths attributed to COVID. “The strategy from the outset should have been implementing protocols to stop hospitalizations through early treatment of Americans who tested positive for COVID but were still asymptomatic. If we had done that, we could have pushed case fatality rates below those we see with seasonal flu, and ended the bottlenecks in our hospitals. We should have rapidly deployed off-the-shelf medications with proven safety records and subjected them to rigorous risk/benefit decision-making,” McCullough continues. “Using repurposed drugs, we could have ended this pandemic by May 2020 and saved 500,000 American lives, but for Dr. Fauci’s hard-headed, tunnel vision on new vaccines and remdesivir.

McCullough observes that, “We could have dramatically reduced COVID fatalities and hospitalizations using early treatment protocols and repurposed drugs including ivermectin and hydroxychloroquine and many, many others.” Dr. McCullough has treated some 2,000 COVID patients with these therapies. McCullough points out that hundreds of peer-reviewed studies now show that early treatment could have averted some 80 percent of deaths attributed to COVID. “The strategy from the outset should have been implementing protocols to stop hospitalizations through early treatment of Americans who tested positive for COVID but were still asymptomatic. If we had done that, we could have pushed case fatality rates below those we see with seasonal flu, and ended the bottlenecks in our hospitals. We should have rapidly deployed off-the-shelf medications with proven safety records and subjected them to rigorous risk/benefit decision-making,” McCullough continues. “Using repurposed drugs, we could have ended this pandemic by May 2020 and saved 500,000 American lives, but for Dr. Fauci’s hard-headed, tunnel vision on new vaccines and remdesivir.

People are scare-mongering about Covid vaccines based on the most tenuous whiff of an issue, and even on fantasies.

Even with all the necessary precautions, you might get infected. But don’t let that lose your faith in safety. Your job is to focus on your actions, the consequences were never in your control anyway.

Thus, if any FDA-approved drug like hydroxychloroquine (or ivermectin) proved effective against COVID, pharmaceutical companies would no longer be legally allowed to fast-track their billion-dollar vaccines to market under Emergency Use Authorization. Instead, vaccines would have to endure the years-long delays that have always accompanied methodical safety and efficacy testing, and that would mean less profits,

Yet an investigation by the BBC programme Panorama discovered the move was at least partly a way to get around the shortage of protective equipment in the NHS. The problem was that the Health and Safety Executive had earlier ruled that the very top level of PPE should be worn when dealing with a disease ranked as an HCID. The change in classification therefore meant health workers could be kitted out with less protective equipment – making the most of the threadbare stocks available. The government had requested that the Advisory Committee on Dangerous Pathogens remove Covid-19 from the HCID list.

This is how we know that Anthony Fauci was well aware of remdesivir’s toxicity when he orchestrated its approval for COVID patients. NIAID sponsored that project. Dr. Fauci had another NIAID-incubated drug, ZMapp, in the same clinical trial, testing efficacy against Ebola alongside two experimental monoclonal antibody drugs. Researchers planned to administer all four drugs to Ebola patients across Africa over a period of four to eight months.10,11 However, six months into the Ebola study, the trial’s Safety Review Board suddenly pulled both remdesivir and ZMapp from the trial.12 Remdesivir, it turned out, was hideously dangerous. Within 28 days, subjects taking remdesivir had lethal side effects including multiple organ failure, acute kidney failure, septic shock, and hypotension, and 54 percent of the remdesivir group died—the highest mortality rate among the four experimental drugs.13 Anthony Fauci’s drug, ZMapp, ran up the second-highest body count at 44 percent. NIAID was the primary funder of this study, and its researchers published the bad news about remdesivir in the New England Journal of Medicine in December 2019.

Compare ivermectin’s safety record to Dr. Fauci’s two chosen COVID remedies, remdesivir (which hospital nurses have dubbed “Run-death-is-near”), and the COVID vaccines. Over 30 years, ivermectin has been associated with only 379 reported deaths, an impressive death/dose reporting ratio of 1/10,584,408. In contrast, over the 18 months since remdesivir received an EUA, about 1.5 million patients have received remdesivir, with 1,499 deaths reported (a dire 1/1,000 D/D ratio). Meanwhile, among recipients of COVID jabs in the US during the ten months following their rollout, some 17,000 deaths have occurred following vaccination, a reported D/D ratio of 1/13,250. Ivermectin, therefore, is thousands of times safer than remdesivir and COVID vaccines. The science also indicates that it is far more effective than either.

I am alive, well and fully vaccinated, despite pledging allegiance to no authority. Listening to experts is not complacency, it's just an act of common sense humanity.

From the outset, hydroxychloroquine (HCQ) and other therapeutics posed an existential threat to Dr. Fauci and Bill Gates’ $48 billion COVID vaccine project, and particularly to their vanity drug remdesivir, in which Gates has a large stake.1 Under federal law, new vaccines and medicines cannot quality for Emergency Use Authorization (EUA) if any existing FDA-approved drug proves effective against the same malady: For FDA to issue an EUA (emergency use authorization), there must be no adequate, approved, and available alternative to the candidate product for diagnosing, preventing, or treating the disease or condition. . . .2 Thus, if any FDA-approved drug like hydroxychloroquine (or ivermectin) proved effective against COVID, pharmaceutical companies would no longer be legally allowed to fast-track their billion-dollar vaccines to market under Emergency Use Authorization. Instead, vaccines would have to endure the years-long delays that have always accompanied methodical safety and efficacy testing, and that would mean less profits, more uncertainty, longer runways to market, and a disappointing end to the lucrative COVID-19 vaccine gold rush. Dr. Fauci has invested $6 billion in taxpayer lucre in the Moderna vaccine alone.3 His agency is co-owner4 of the patent and stands to collect a fortune in royalties. At least four of Fauci’s hand-picked deputies are in line to collect royalties of $150,000/year based on Moderna’s success, and that’s on top of the salaries already paid by the American public.5,6

Under federal law, new vaccines and medicines cannot quality for Emergency Use Authorization (EUA) if any existing FDA-approved drug proves effective against the same malady: For FDA to issue an EUA (emergency use authorization), there must be no adequate, approved, and available alternative to the candidate product for diagnosing, preventing, or treating the disease or condition. . . .2 Thus, if any FDA-approved drug like hydroxychloroquine (or ivermectin) proved effective against COVID, pharmaceutical companies would no longer be legally allowed to fast-track their billion-dollar vaccines to market under Emergency Use Authorization. Instead, vaccines would have to endure the years-long delays that have always accompanied methodical safety and efficacy testing, and that would mean less profits, more uncertainty, longer runways to market, and a disappointing end to the lucrative COVID-19 vaccine gold rush. Dr. Fauci has invested $6 billion in taxpayer lucre in the Moderna vaccine alone.3 His agency is co-owner4 of the patent and stands to collect a fortune in royalties. At least four of Fauci’s hand-picked deputies are in line to collect royalties of $150,000/year based on Moderna’s success, and that’s on top of the salaries already paid by the American public.5

Compare ivermectin’s safety record to Dr. Fauci’s two chosen COVID remedies, remdesivir (which hospital nurses have dubbed “Run-death-is-near”), and the COVID vaccines.

Florida: Bad at COVID-19, hurricane evacuations and health and safety.

It was the first responders who put their bodies in harm’s way for the safety of my colleagues and acquaintances. But when it came to it, when it came to protecting the bodies of first responders from coercion and harm, the “Zoom class” failed utterly to reciprocate with courage of their own. To say the least, in this time of testing, we have not all been equally brave.

We live in a crazy world, where people feel trapped when they are asked to live in their own home for their own safety.

Fear not, get your shot.

naturally consider Dr. Mercola to be Public Enemy #1. Big Pharma’s $9.6 billion annual advertising budget gives these unscrupulous companies control over our news and television outlets. Strong economic drivers (pharmaceutical companies are the biggest network advertisers) have long discouraged mainstream media outlets from criticizing vaccine manufacturers. In 2014, a network president, Roger Ailes, told me he would fire any of his news show hosts who allowed me to talk about vaccine safety on air. “Our news division,” he explained, “gets up to 70% of ad revenues from pharma in non-election years.

The Vaccine Sonnet Listen to the experts, Listen to Fauci. Grow up you big sissy, Enough with the ouchie! I got the vaccine, Trust me it's safe. Every scientist will confirm, Listen to reason not hearsay. Vaccines produce immunity, Masks prevent the spread. If you follow some simple steps, You'll prevent someone's death. Freedom without reason is savagery. During pandemic accountability is key.

If any FDA-approved drug like hydroxychloroquine (or ivermectin) proved effective against COVID, pharmaceutical companies would no longer be legally allowed to fast-track their billion-dollar vaccines to market under Emergency Use Authorization. Instead, vaccines would have to endure the years-long delays that have always accompanied methodical safety and efficacy testing, and that would mean less profits, more uncertainty, longer runways to market, and a disappointing end to the lucrative COVID-19 vaccine gold rush. Dr. Fauci has invested $6 billion in taxpayer lucre in the Moderna vaccine alone. His agency is co-owner of the patent and stands to collect a fortune in royalties. At least four of Fauci’s hand-picked deputies are in line to collect royalties of $150,000/year based on Moderna’s success, and that’s on top of the salaries already paid by the American public.

You can choose to take the Vaccine, or you can choose not to take the Vaccine. The choice is yours, but don’t go around forcing your choices on to others. You have every right to choose what you want, but every right comes with responsibility. You are responsible for your own safety and safety of others. Whatever the outcome is. You should be held accountable for your actions or choices and don’t choose to hate on others for making different choices than the one you made.

Instead, vaccines would have to endure the years-long delays that have always accompanied methodical safety and efficacy testing, and that would mean less profits, more uncertainty, longer runways to market, and a disappointing end to the lucrative COVID-19 vaccine gold rush. Dr. Fauci has invested $6 billion in taxpayer lucre in the Moderna vaccine alone.3 His agency is co-owner4 of the patent and stands to collect a fortune in royalties. At least four of Fauci’s hand-picked deputies are in line to collect royalties of $150,000/year based on Moderna’s success, and that’s on top of the salaries already paid by the American public.5,6

Perhaps it does come back to valuing community, after all. Recent studies in science communication have suggested what I've sketched out in this chapter: that scientific literacy is not the variable that determines whether or not a group will accept the reality of a public health issue like vaccination or global warning: social groups are. While those individuals tested demonstrated a surprising ability to factually interpret scientific findings, they tended to eventually revert to in-group thinking about the issue, siding with whatever their main social group already believed. We humans are social, after all. Our social nature is why solitary confinement is potentially a human rights violation, why just about all of us wish we weren't having to stay home during the COVID crisis, why we all cling to Zoom meetings-why children yell at one another across balconies, starved for the sound of another child's voice. We all do the same dance of retreating to our social safety spaces. And if our 'safe' social group told us that our experience during the pandemic was a lie? Well, it seems we'd be more likely to believe our friends than science, because, as I've argued elsewhere...in times of desperate calamity, all we humans really have is one another. I have no answer to this twisted dilemma that the healthy carrier narrative, via the vehicle of COVID-19, has presented to us in the United States, but understanding the dilemma rightly is surely important.

Other life-forms exist and have consciousness. Their lives give us a lot of food for nutrition and food for thought. We get food for our physical needs from plants, trees and farm animals. We are able to use some animals for our safety and travel. Even the microorganisms are important in decomposing waste and are a source of medicines and vaccines. In a way, these life-forms support our sustenance. Humans as consumers depend on nature for their sustenance more so than the plants which produce their own food and supply nutrients for other animals including humans.

The fact that my 75 year-old Asian mom has two shots of the Moderna vaccine in her arm makes me want to cry. The fact that my 75 year-old Asian mom no longer feels safe walking down the street by herself also makes me want to cry. #America (3/31/2021 on Twitter)

In the midst of a pandemic, with hundreds of thousands of deaths attributed to COVID, and the economy in free fall, Dr. Fauci’s suggestion that we withhold promising treatments that have an established safety profile—from patients who have a potentially lethal disease—pending the completion of randomized controlled clinical trials, is highly manipulative and utterly unethical. It is not medically ethical to allow a COVID-19 patient to deteriorate in the early stages of the infection when there is an inexpensive, safe, and demonstrably effective HCQ treatment that CDC’s and NIAID’s own studies show blocks coronavirus replication. It would be equally unethical to enroll sick individuals in such studies—as Dr. Fauci proposes—in which half the infected patients would receive a placebo.

If u want ppl 2 deliver u groceries & goods but don't want to hold the corporations they work for accountable for PPE, thriving wages, hazard pay, & taxes, you're exploiting cheap labor for your own safety. We won't survive on exploitation. We only survive through solidarity. (4/1/2020 on Twitter)

Dr. Fauci’s insider’s cabal greased the skids, allowing Burroughs Wellcome to skip animal testing and to proceed directly to human trials. This omission was unprecedented in the history of chemotherapy drugs, but again foreshadowed the decision to allow the Pfizer/BioNTech COVID-19 vaccine to proceed to human testing without completing the usual panel of safety testing in animal models.

Notably, we now know that Daszak, Baric, and Wuhan Institute of Virology director Shi Zhengli collaborated on a 2018 proposal to the Defense Department’s research and development agency, Defense Advanced Research Projects Agency (DARPA), “to collect SARS-like bat coronaviruses and insert a genetic component,” the furin cleavage site, to “enable them to more easily infect human cells.”68 The grant application was called “Project Defuse: Defusing the Threat of Bat-Borne Coronaviruses.” Emails subsequently obtained by U.S. Right to Know reveal that Daszak downplayed the Wuhan Institute’s role likely so as to avoid triggering concerns about biosafety, though “a lot of these assays can be done in Wuhan” and that doing them under the Wuhan Institute’s relatively lax biosafety level 2 conditions “makes our system highly cost-effective relative to other bat-virus systems.” Baric, whose University of North Carolina lab would conduct such research at a much more demanding biosecurity level 4, pointed out that in the United States, such research required at least level 3, especially when the viruses are able “to bind and replicate in primary human cells.” Noting China’s lax safety standards, Baric’s marginal comment in the draft grant application was: “US researchers will likely freak out.”69

The lackluster response by the USA to COVID-19 is comparable to what I observed in the OSHA health and safety system.

It is important that nurses and doctors know that failing to use legally required health and safety protocols with COVID-19 patients may invalidate their disability and life insurance policies.

I have spent over a decade observing the government and concluded they are willfully incompetent in the health and safety of their citizens.

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allowing Burroughs Wellcome to skip animal testing and to proceed directly to human trials. This omission was unprecedented in the history of chemotherapy drugs, but again foreshadowed the decision to allow the Pfizer/BioNTech COVID-19 vaccine to proceed to human testing without completing the usual panel of safety testing in animal models.82 Government researchers had thoroughly assessed AZT’s frightening toxicity, including its lethal effects on rodents after short-term exposures with minuscule doses.

Thus, if any FDA-approved drug like hydroxychloroquine (or ivermectin) proved effective against COVID, pharmaceutical companies would no longer be legally allowed to fast-track their billion-dollar vaccines to market under Emergency Use Authorization. Instead, vaccines would have to endure the years-long delays that have always accompanied methodical safety and efficacy testing, and that would mean less profits, more uncertainty, longer runways to market, and a disappointing end to the lucrative COVID-19 vaccine gold rush. Dr. Fauci has invested $6 billion in taxpayer lucre in the Moderna vaccine alone.3 His agency is co-owner4 of the patent and stands to collect a fortune in royalties. At least four of Fauci’s hand-picked deputies are in line to collect royalties of $150,000/year based on Moderna’s success, and that’s on top of the salaries already paid by the American public.

In that sense, an unbroken devolution of FDA’s regulatory function leads from AZT to the fraud-fueled “Emergency use approvals” of remdesivir and the Moderna mRNA vaccine during the COVID pandemic. “The death blow to FDA’s safety function was AZT,” says Farber. “After that, any potentially deadly disease became an excuse for curtailing clinical trials.

The need to satisfy FDA and NIH rules can also slow down important biomedical research, ultimately costing lives. In fall 2020, Moderna announced it was slowing enrollment in its clinical trial of a COVID-19 vaccine to ensure it had sufficient minority representation among study participants. As thousands of people worldwide were dying of COVID-19-related ailments, Moderna CEO Stéphane Bancel made the remarkable assertion that diversity in research subjects “matters more to [Moderna] than speed.”55 NIH director Francis Collins later revealed that Moderna was not acting autonomously but rather under his direction.56 He told Moderna that it needed to recruit more “people of color” (i.e., people other than non-Hispanic whites), before NIH would acknowledge the vaccine’s safety.

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