Tooth Fairy, Santa Claus and Anthony Fauci
Segment # 055
What's the difference - Santa Claus and the Tooth Fairy are more believable
COVID-19 Vaccine Effectiveness Plunges Against Omicron: CDC Data
By Zachary Stieber
September 1, 2022 Updated: September 1, 2022
“COVID-19 vaccine effectiveness for all age groups has been much worse against the Omicron virus variants than earlier strains, particularly the currently dominant subvariants, according to U.S. Centers for Disease Control and Prevention (CDC) data presented on Sept. 1.
The data, much of which hasn’t been previously published, show that the protection against both symptomatic infection and severe disease isn’t as strong against Omicron, which emerged in December 2021, and its subvariants.
Data from the CDC’s Increasing Community Access to Testing, a no-cost testing program, showed that vaccine effectiveness for a booster compared to a primary series against symptomatic infection waned rapidly across all age groups, going under 50 percent within two months and turning negative around six months.
A fourth dose, or second booster, upped the protection, but the shielding quickly dropped to less than 40 percent, according to estimates for those 50 and older.
Estimates drawn from the CDC’s VISION Network showed that emergency department and urgent care visits rose over time for the vaccinated, with adjusted vaccine effectiveness estimates for 5- to 11-year-olds dropping to 18 percent 150 days or more after the second shot from just 51 percent 14 to 59 days after a primary series.”
In essence what they promised and what they delivered was pure nonsense and definitely not science. I cannot imagine a scenario where the CDC and the FDA could have earned LESS CREDIBLITY than they have on this issue. And yet millions of Americans of all ages are about to step up for what could be their fifth shot without proof of efficacy with human testing. That’s flat out NUTs considering that the hospitalization and mortality rate among the youngest victims is almost zero.
Millennials Experienced ’84 Percent Rise of Excess Mortality’ Into Fall 2021: Former BlackRock Portfolio Manager
Excess deaths after government’s vaccine mandates must be talked about: author Edward Dowd
Edward Dowd, a former portfolio manager for BlackRock and the author of the upcoming book “’Cause Unknown’: The Epidemic of Sudden Deaths in 2021 & 2022,” has been analyzing data related to all-cause mortality since March 2021.
Dowd is familiar with predicting trends and observing patterns, and became interested in studying CDC data after he heard many anecdotal accounts of vaccine injury. He found a monumental spike in sudden deaths occurring in the fall of 2021 to early 2022 in the working age cohort, which corresponded to the Biden administration’s vaccine mandates for federal and corporate employees.
“The age cohort from 25 to 44, which we call the millennials, experienced an 84 percent rise of excess mortality into the fall of 2021—August, September, October—and the rate of change was just dramatic,” Dowd told EpochTV’s American Thought Leaders program during an interview that will premiere Sept. 6. That “represented about 61,000 Americans who perished from March 2021 to February 2022.”
“They did what’s called a Group Life survey, where they rolled out about 80 percent of the revenues of the industry and looked at some all-cause mortality data. [I was pointed] to table 5.7, which is on page 23 of this report,” said Dowd.
“In the 25 to 34 [age group], they saw 78 percent excess mortality in the third quarter of 2021. They also saw in the 35 to 44 age group 100 percent excess mortality. We combined that group and our number was 84 percent,” said Dowd.
Dowd said the fact that they used different data sets—Dowd used CDC all-cause mortality numbers and the insurance company used their group life claim numbers—but got similar death spikes, validates his hypothesis of vaccines being the cause of death.
“But we need more data from the government, which they’re not providing. And if they did, the link would be there, I think, 100 percent,” said Dowd.
Horowitz: COVID vaccines vs. ivermectin: Night vs. day and the Rosetta stone of the motivations behind COVID fascism
Under what sort of circumstance would you approve a variant of a shot based on a study of eight mice? Well, for one, it would have to be an emergency. It would also have to be a variant of a therapeutic that already has an impeccable record of safety … you know, like ivermectin. In reality, the more the virus is becoming less of an emergency and the more the original vaccines turn out to be dangerous and ineffective beyond belief, the more the medical and government establishment lowers the standards for additional vaccines, while continuing to declare war on proven therapeutics like ivermectin.
Imagine people dying in the thousands with no treatment, and the establishment refuses to use a broad-spectrum anti-inflammatory that doctors all over the world have witnessed helping restore people’s blood oxygen level during a cytokine storm. No! This cannot be used despite winning a Nobel Prize and being designated as an essential drug because we didn’t have large randomized controlled trials vouching for its efficacy (even though its safety was already established). Well, evidently, RCTs are only for drugs already proven safe, not for gene therapies already proven unsafe. Those can be approved simply based on mice tests for a variant that is not an emergency under anyone’s definition.
Just consider what we know about the existing shots. The one-of-a-kind study of all-cause severe adverse events of interest co-written by British Medical Journal editor Peter Doshi has been published in Vaccine, and its results are as revealing as they are shocking. The authors found a straight-up negative cost-benefit analysis among the participants in the Pfizer and Moderna trials. Specifically, Dr. Doshi and his colleagues found that the Pfizer shot was associated with an increased risk of serious “adverse events of special interest” of 10.1 events per 10,000 vaccinated for Pfizer and 15.1 per 10,000 for Moderna.
An adverse event of special interest is defined as death, life-threatening injury at the time of the event, inpatient hospitalization or prolongation of existing hospitalization, or persistent or significant disability/incapacity, among several other criteria. The average between the two shots works out to 1 in 800 people, which would total approximately 448,000 people in the U.S. and 10.6 million globally, based on vaccination rates. But keep in mind, the follow-up period for trial participants was short because the participants were then unblinded and vaccinated. The long-term severe adverse events and sudden deaths are likely even higher. Also, this analysis doesn’t factor in all the people who subsequently got boosters. This shot is clearly dose-dependent, increasing the risk of death or injury with every dose.
Yet, to this day, this shot is still mandated on the military, health care workers, and many others, including pregnant women and schoolchildren in some circumstances. Now, as it becomes clear the virus has attenuated and the shots don’t work and are dangerous, the establishment is approving new versions of the same technology – with the extremely pro-inflammatory lipid nanoparticles and spike protein – just based on mice studies.
In contrast, let’s take a look at two new studies that came out concerning use of ivermectin for this virus. Brazilian doctors published the second half of their massive observational study on ivermectin use in Itajaí, a city in Santa Catarina, Brazil. It is the largest study of any COVID therapeutic, involving 113,844 who used ivermectin prophylactically and 45,716 who did not. The first half of the study, published late last year, found the relative risk reduction in mortality rate among those high-risk people taking ivermectin was 71% among those with type 2 diabetes and 67% among those with hypertension. The absolute risk reduction was also even greater among older people who are most at risk. This was the most transparent study done on COVID treatment because all information about every single patient was uploaded online for researchers to scrutinize.
This week, the same researchers published part two of the same study in Cureus, which evaluated whether the regular use and the total amount of ivermectin used provided greater benefit, meaning researchers wanted to ascertain the degree of dose dependency of ivermectin in combating COVID. They divided the ivermectin group into two sub-groups: those who took a total of 60mg during the study period (defined as irregular users) and those who took a cumulative total of 180mg (defined as regular users). The results were astounding and proved a clear dose dependency.
The hospitalization rate was reduced by 100% in regular users compared to both irregular users and non-users (p < 0.0001), and by 29% among irregular users compared to non-users (RR: 0.781; 95% CI: 0.49-1.05; p = 0.099). Mortality rate was 92% lower in regular users than non-users (RR: 0.08; 95% CI: 0.02-0.35; p = 0.0008) and 84% lower than irregular users (RR: 0.16; 95% CI: 0.04-0.71; p = 0.016), while irregular users had a 37% lower mortality rate reduction than non-users (RR: 0.67; 95% CI: 0.40-0.99; p = 0.049). Risk of dying from COVID-19 was 86% lower among regular users than non-users (RR: 0.14; 95% CI: 0.03-0.57; p = 0.006), and 72% lower than irregular users (RR: 0.28; 95% CI: 0.07-1.18; p = 0.083), while irregular users had a 51% reduction compared to non-users (RR: 0.49; 95% CI: 0.32-0.76; p = 0.001) (emphasis added).
Again, this was a massive study sample with the most transparent data and crosstabs of any study. Moreover, although it wasn’t a randomized controlled trial, the fact that it was unblinded helped researchers see that the higher-risk people actually chose to take ivermectin, and the more regular usage of it within the ivermectin cohort. “Non-use of ivermectin was associated with a 12.5-fold increase in mortality rate and a seven-fold increased risk of dying from COVID-19 compared to the regular use of ivermectin,” concluded the researchers. “This dose-response efficacy reinforces the prophylactic effects of ivermectin against COVID-19.”
One of the lead authors, endocrinologist Dr. Flavio Cadegiani, has treated thousands of patients with an ivermectin and nitazoxanide-based protocol and has not lost a single patient. Yet rather than being treated like a hero, he has been accused of crimes against humanity. TrialSiteNews reports that Dr. Cadegiani’s clinic and private residence were raided by police who were searching for documents related to research from one of his other treatment regimens.
Again, behold the contrast between the treatment of safe, off-patent drugs and novel, expensive therapies. The latter are mandated, while the former are nearly criminalized.
Even the NIH has ivermectin listed on its website as a proposed COVID treatment and notes that it is “widely used and is generally well-tolerated” and “may interfere with SARS-CoV-2 spike protein attachment to the human cell membrane,” while having “anti-inflammatory properties…beneficial in people w/COVID-19.”
Which brings us to the second ivermectin study published this week, which focuses on severely ill patients in respiratory distress. Like Dr. Cadegiani, Dr. Jackie Stone, a family medicine physician based in Harare, Zimbabwe, barreled head-first into treating COVID from day one, conducted studies on her patient outcomes, and is being punished for her work. She co-authored a paper in Biologics showing a 62% normalization rate of blood oxygen levels of 34 severely ill COVID patients within 24 hours after being treated with ivermectin, doxycycline, and zinc. While 34 is not a large sample size, one cannot miss the unmistakable sudden surge in the pulse oximeter of those who took ivermectin during the critical hours of the cytokine storm eating away at the lungs.
As the authors note: “All but two of the 34 patients in this study had increases in SpO2 within the first 48 h after the first dose of IVM. This overall increase in SpO2 continued throughout the entire observation period. Because SpO2 values that are at best stable and typically decreasing for several days after onset of disease symptoms are a well-established norm for moderate and severe COVID-19 patients under standard care,…these sharp, rapid SpO2 increases for all but two of the 34 patients in this study are noteworthy.”
Dr. Stone’s reward for her devotion to her patients? She is facing criminal charges in court. So what is going on?
Even if one wants to scoff at these studies and believe the pharma-contrived studies that ivermectin has less efficacy, nobody could deny the fact that it is safe. So, what is there to lose? How could one square the mentality of rushing into a known dangerous shot even for children and pregnant women based on mice trials, but treating one of the safest drugs like poison?
The questions answer themselves.
