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September 26 - October 18, 2024
By this decade’s end, obesity, diabetes, and pre-diabetes are on track to debilitate 85 percent of America’s citizens.
Furthermore, some 52 studies—all available on NIH’s website—find that ordinary masking (using less than an N95 respirator) doesn’t reduce viral infection rates, even—surprisingly—in institutional settings like hospitals and surgical theaters.
CDC later admitted that only 6 percent of COVID deaths occurred in entirely healthy individuals. The remaining 94 percent suffered from an average of 3.8 potentially fatal comorbidities.24
Regulators misused PCR tests that CDC belatedly admitted in August 2021 were incapable of distinguishing COVID from other viral illnesses.
CDC also refused to conduct follow-up medical inquiries among people claiming vaccine injuries.
(78 percent of Americans hospitalized for COVID-19 were overweight or obese).
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.
COVID deaths dropped precipitously—by 14-fold—in the regions where the Peruvian government effectively distributed ivermectin.
A December 2020 study showed that African and Asian countries that widely used ivermectin to treat and prevent various parasitic diseases enjoy some of the world’s lowest-reported COVID case and mortality rates.
By September, the Uttar Pradesh government announced that the state’s 33 districts are virtually devoid of active cases, despite having a vaccination rate of only 5.8 percent.49 The Hindustan Times reported, “Overall, the state has a total of 199 active cases, while the positivity rate came down to less than 0.01 per cent. The recovery rate, meanwhile, has improved to 98.7 per cent.”50 When America’s vaccination rate was at 54 percent, cases were still rising and governments were still imposing draconian restrictions. As of August 10, 2021, the United States saw 161,990 new cases and 1,049 new
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Demonizing IVM as a “horse drug” was, of course, ironic, given that NIAID initially developed Merck’s replacement therapy, molnupiravir, as a horse drug.
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).
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.
Remdesivir has no clinical efficacy against COVID, according to every legitimate study. Worse, it is deadly poisonous, and expensive poison at $3,000 for treatment.
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.
Before his study was completed or peer-reviewed, much less published, Dr. Fauci learned that The Lancet had just published a placebo-controlled Chinese study that showed remdesivir utterly ineffective at keeping hospitalized patients alive OR reducing the duration of hospitalizations.48 Even more importantly, remdesivir did not reduce the presence of the virus in the blood. Worst of all, the Chinese study confirmed remdesivir’s deadly toxicity.
In the WHO’s trial, remdesivir failed to reduce mortality, and failed to reduce the need for ventilators OR the length of hospital stays. WHO researchers found no detectable benefits from remdesivir and recommended against its use in COVID-19 patients.
On July 15, 2021, a large Johns Hopkins Study in Original Investigation | Infectious Diseases once again confirmed that “Remdesivir treatment was not associated with improved survival but was associated with longer hospital stays.”72 (Emphasis added.)
remdesivir causes extreme toxicity to lungs and kidneys,78 and mimics several of the other lethal symptoms of COVID, including multi-organ failure.79 Many doctors believe our country’s record COVID-19 fatalities are at least in part due to widespread use of remdesivir in 2020.
For several months, we were the only country treating people with a drug proven to be lethal. That year, 2020, we had almost double the number of deaths per month compared to most other countries. Brazil, one of the first nations to widely use remdesivir, had the second highest death toll.
Even worse, vaccinated individuals, he warned, would become asymptomatic carriers and “mutant factories” blasting out vaccine-resistant versions of the disease that were likely to lengthen and intensify rather than abbreviate the pandemic.
[B]inding antibodies can be dangerous and cause something called Antibody Dependent Enhancement. And we’ve seen that. I mean, we saw that with the [Gates-funded] dengue vaccine. But with the dengue vaccine, in children who had never been exposed to dengue before, it actually made them worse when they were then exposed to the natural virus. Much worse. Vaccinated children who were less than nine years of age, who had never been exposed to dengue before, were more likely to die if they’d been vaccinated than if they hadn’t been vaccinated.12
AHRQ initially planned to roll out the system to all remaining HMOs, but after seeing the AHRQ’s frightening results—vaccines were causing serious injuries in 1 of every 40 recipients—CDC killed the project and stowed the new system on a dusty shelf.
“Anthony Fauci is a great guy in the same way that Harvey Weinstein was a great guy,”
The final summary of the Pfizer’s six-month clinical trial data—the document that Pfizer submitted to FDA to win approval—revealed one key data point that should have killed that intervention forever. Far more people died in the vaccine group than in the placebo group during Pfizer’s clinical trials. The fact that FDA nevertheless granted Pfizer full approval, and that the medical community embraced and prescribed this intervention for their patients, is eloquent testimony to the resilience of even the most deadly and inefficacious products, and the breathtaking power of the pharmaceutical
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Pfizer’s six-month clinical data for its COVID vaccine trials suggested that, while the vaccine would avert a single death from COVID-19, the vaccinated group suffered 4x the number of lethal heart attacks as the unvaccinated.
The world’s most vaccinated nation, Gibraltar, aggressively inoculated its 34,000 inhabitants, achieving 115 percent coverage (officials also vaccinated Spanish tourists) by July 2021. In December 2020, prior to the vaccine rollout, Gibraltar’s health agency had experienced only 1,040 confirmed cases and five deaths from COVID-19. After the vaccination blitz, the number of new infections increased fivefold—to 5,314—and the number of deaths increased nineteen-fold.
NEGATIVE VACCINE EFFECTIVENESS of -53 percent for the over-40 age group. Reported infections are highest in the double-vaccinated. This means that fully vaccinated individuals from this age group experienced a 53 percent HIGHER reported infection rate than the unvaccinated that month.
One of CDC’s bold deceptions is to hide vaccine mortalities in US data by counting all people as “unvaccinated” unless their deaths occur more than two weeks AFTER the second vaccine.75 (Ironically, CDC doubles down on this fraud by counting many of these vaccine deaths as COVID deaths.) In this way, CDC captures that wave of deaths that occurs after vaccination and attributes them all to “unvaccinated.” This is only one of many statistical chicaneries that the CDC employs to hide vaccine injuries and to stoke public fears of COVID.
Israeli data and US data presented to CDC’s advisory committee on June 23, 2021 similarly found the rate of reported cases of myocarditis in vaccinated teenage boys aged 12–17 is at least twenty-five times greater than expected, and is fifty times greater than the reported rate in vaccinated males over 65.
A recent study suggests that myocarditis is associated with a 50 percent mortality within five years.
Some 86 percent of children suffered an adverse reaction to the Pfizer COVID vaccine in clinical trial. And one in nine children suffered a serious reaction grave enough to leave them unable to perform daily activities.
In July 2021, the CDC found that fully vaccinated individuals who contract the infection have as high a viral load in their nasal passages as unvaccinated individuals who get infected. This means the vaccinated are just as infectious as the unvaccinated.
“each vaccinated person is now a kind of Typhoid Mary for COVID, spreading concentrated viral loads of vaccine resistant mutants to vaccinated and unvaccinated alike.”
Dr. Fauci then overlooked Gilead’s price gouging; the company sold remdesivir for $3,300–$5,000 per dose, during the COVID pandemic. The raw materials to make remdesivir cost Gilead under $10.
An exhaustive 2000 study by CDC and Johns Hopkins scientists published in Pediatrics, the official journal of the American Academy of Pediatrics, concluded, “Thus vaccination does not account for the impressive declines in [infectious disease] mortality seen in the first half of the [20th] century . . . nearly 90 percent of the decline in infectious disease mortality among US children occurred before 1940, when few antibiotics or vaccines were available.”
Merck maintained it had not tested either vaccine against an inert placebo in pre-approval trials, so no one could scientifically predict if the vaccines would avert more injuries or cancers than they would cause. Nevertheless, the sister FDA panel, VRBPAC, approved Gardasil—to prevent cervical cancer—without requiring proof that the vaccine prevented any sort of cancer, and despite strong evidence from Merck’s clinical trial that Gardasil could dramatically raise risks of cancer and autoimmunity in some girls.
Despite years of pleading by the HIV community, Dr. Fauci refused to test any of those repurposed drugs, which had older or expired patents and no Pharma patrons.11 One of the most promising of these “street drugs” was AL 721, an antiviral that was far less toxic than AZT. Two of Dr. Fauci’s top scientists, Robert Gallo and Jeffrey Laurence from NCI, had found AL 721 effective in reducing HIV viral loads—but, under pressure from his phalanx of Burroughs Wellcome PIs, Dr. Fauci refused to follow up.12 Big Pharma and its PIs were loath to test any drug with patents they didn’t control. None of
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At first, his devious plan backfired. Instead of debunking AL 721, the NIAID study confirmed that AL 721 stopped viral replication. When those promising results began emerging, Dr. Fauci and his PIs cancelled the trial, making sure that AL 721 never went to Phase 2. Dr. Fauci told skeptical activists that he could not get any volunteers to enroll in the study. (In 2021, he would invoke the same bunko to kill NIAID’s ivermectin trials.)
The rules of the trials clearly stated that the PIs must record all adverse reactions on their CRFs and report immediately to the FDA. The Boston PIs did neither. The FDA documents showed that the PIs knew very well which patients were on AZT and which on placebo, that they were skewing safety results in AZT’s favor to give advantage to the AZT participants. Researchers began by placing the sickest patients in the placebo group. The researchers then bent over backward to coddle the group that took AZT, giving them more supportive medical services than the placebo subjects. For example,
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The vaccine manufacturers acknowledge that the products are not tested for effects on fertility.
Dr. Fauci achieved that feat by allowing Merck to run Crixivan through a skeleton CRI process on a tiny cohort of ninety-seven volunteers in three groups, thereby winning the swiftest approval in history: forty-two days.
Conversely, there are thousands of known AIDS cases in patients who are not demonstrably infected with HIV.
Asked to define AIDS in a 2009 documentary, Fauci said, “When your CD4 count falls below a certain arbitrary level, by definition you have AIDS.”40 But how do we explain the many individuals who have low CD4 counts and no HIV?
Scientists were shocked to learn for the first time that Gallo had found faint traces of HIV in only twenty-six of the seventy-two AIDS patients whose blood he examined.
However, since it is unclear whether Gallo or any other researcher was ever able to isolate HIV,60 he took from his AIDS patients a sample of antibodies that he found in great abundance in their blood and made a leap of faith that they were HIV antibodies. Geneticists have pointed out that these antibodies may have been associated with tuberculosis or herpes, or any of the many other pathogenic illnesses that multiply in collapsing immune systems.61 Indeed, Gallo’s HIV antibody test also reacts to people with fever, pregnant women, and individuals who have overcome a tuberculosis infection.
HIV has proven barely to be found in AIDS patients even in the final throes of illness.
neither Dr. Fauci nor Gallo has ever credibly explained the fact that viral load from HIV is always at its greatest in the days immediately following infection. Logically, it would be during this period that the virus is most likely to cause devastating illness. And yet, the onset of AIDS symptoms almost always arrive decades later (an average twenty years following exposure)—when viral loads are at their lowest.
Researchers believe poppers to be the direct cause of Kaposi’s sarcoma, a rare form of skin cancer that afflicts the nose, throat, lungs, and skin.77 Kaposi’s sarcoma was the initial indicator disease of AIDS, but it was also common in gay men who were not infected with HIV.
His laboratory had demonstrated that in culture with his new mycoplasma, HIV becomes a vicious killer. Montagnier declared that he now believes that HIV is “a peaceful virus” that becomes lethal only when combined with mycoplasma infertans.
