COVID-19 / Malicious Medical Quackery
[Ed.: FEAR YOUR DOCTOR! Medicine is a disgraced profession. They cannot (and must not) be trusted any longer! Cultivate Nosocomephobia and iatrophobia. Spread ‘vaccine hesitancy’!]
Latest DEATHVAX™ Disability Data 2ND SMARTEST GUY IN THE WORLD
DEC 10, 2023 – This Substack has previously covered the slow kill bioweapon death and disease adverse events…
…and now we have the latest disability data from the U.S. Bureau of Labor Statistic (B[L]S) for November, which further reinforces the horrendous trends.
Disabilities for the entire US population are up 299k:
Just How Far Will the FDA Go To Protect A Bad Drug? A MIDWESTERN DOCTOR
What the tragic lessons of the SSRI antidepressants can teach us about the COVID-19 vaccines
DEC 10, 2023
Story at a Glance:
•The SSRI antidepressants are some of the most harmful medications on the market, but also some of the most profitable.
•Since their discovery, a deluge of data has shown that they are incredibly unsafe, and as one whistleblower testified, overt bribery was needed for the first SSRI, Prozac, to be approved.
•While the FDA initially tried to stop Prozac, once Bush came to power (as his family was in bed with Prozac’s manufacturer), the FDA reversed course.
•Since that time, the FDA has gone to extremely lengths to cover up the harms of antidepressants. Much of what the FDA did with the SSRIs was identical to what it’s done with the COVID vaccines and I believe learning what happened in the past is highly instructive for understanding what the FDA is doing now and how to stop it.
Every now and then, a highly profitable pharmaceutical will come along that everyone also knows is quite dangerous. Remarkably, rather than this stopping the product, it will often be pushed to market and the profits it generates will be used to ensure any objections to its safety get ignored and blown to the wayside.
Law Team Pushes State COVID Mandates up to Supremes by Bob Unruh
Dec. 10, 2023 11:20 am – ‘Orwellian contact tracing program violates fundamental constitutional rights’
The American Freedom Law Center has decided to push state COVID mandates, those thought to violate the constitutional rights of residents, up to the Supreme Court.
The AFLC has filed a petition asking the court to overturn a decision by the 3rd U.S. Circuit Court of Appeals.
Gold, Faith, and Financial Freedom — How A Faith-Based Company Is Transforming Retirement Portfolios
The original case challenged Pennsylvania’s COVID rules, and dates back to 2020 already.
In it, four state residents objected to “the Orwellian contact tracing program and mandate to wear masks, claiming that these restrictions violate fundamental constitutional rights.”
The petition explained, “The COVID-19 pandemic created a constitutional crisis. For years, American citizens, including Petitioners, were subject to constantly changing orders that imposed burdens on fundamental freedoms in a way that our nation has never experienced in its history. The cost of these burdens is incalculable. Unfortunately, many courts did nothing, abdicating their duty to say what the law is and allowing this assault on liberty to proceed largely unchecked.”
It continued, “‘Determination by the [government] of what constitutes proper exercise of police power is not final or conclusive but is subject to supervision by the courts.’ … But this supervision is only effective if the courts are willing to exercise their authority to decide important constitutional questions. Unfortunately, the Courts’ justiciability doctrines (standing, ripeness, mootness) have become convenient excuses for lower courts to surrender their duty to say what the law is, particularly when dealing with the draconian and historic restrictions imposed during the recent pandemic.”
The case was against the governor, the attorney general and secretary of health.
[Ed.: Since this has nothing to do with (Presidential) election fraud, SCOTUS might as well take a look at it, no?]
DEVELOPING: Florida’s Surgeon General Joseph Ladapo Confirms Detection of DNA Fragments in COVID mRNA Vaccines By Jim Hᴏft
Dec. 10, 2023 11:00 am – The Florida Surgeon General, Dr. Joseph A. Ladapo, is demanding answers from Dr. Robert M. Califf, the Commissioner of the U.S. Food and Drug Administration (FDA), regarding the detection of host cell DNA fragments in mRNA COVID-19 vaccines developed by Pfizer and Moderna.
The Florida Surgeon General sent a letter to FDA Commissioner Califf and CDC Director Mandy Cohen on December 6, pressing for greater transparency about the potential for DNA integration into the human genome—a concern that could have far-reaching implications.
The Florida Public Health Integrity Committee discussed these issues on November 14, 2023, and Ladapo urged the FDA to consider their findings. In addition, he reminded Califf of a previous communication dated May 10, 2023, which had yet to receive a response.
On May 10, Ladapo sent a letter to Califf and former CDC Director Rochelle Walensky regarding the risks of the experimental COVID-19 vaccines.
The letter reads:
Here We Go: Nebraska Begins Mass Collection of Digital Health Data on All its Citizens By Jim Hᴏft
Dec. 10, 2023 8:30 am – In an unprecedented move that has chilling implications for personal privacy, the State of Nebraska has begun the mass collection of digital health data on all its citizens, Reclaim The Net reported.
This initiative, part of a state Health Information Technology (HIT) Board’s mandate, consolidates health records in a way that has never been done before, raising alarm over the state’s direction toward a possible national digital ID system and the specter of surveillance that could follow.
The Nebraska Legislature made a law (LB 411) that says all healthcare facilities must share their health records in this system to help patients and improve how healthcare works together.
But, if a facility finds it too hard or impossible to do this because of tech issues, they need to fill out a waiver to explain their situation. The Health Information Technology Board will look at their reasons and decide if they can be excused from joining this system.
Centralized under the auspices of CyncHealth, the health data of over five million patients from 1,100 healthcare institutions are being compiled into a single, sprawling digital database.
Dr. Peter McCullough Urges Preparedness on News of Chinese Pneumonia Outbreak
While the initiative is championed by some for its potential to streamline healthcare and improve medical outcomes, a growing cohort of privacy advocates and concerned citizens are sounding the alarm about the grave implications this broad data collection could have on the sanctity of personal information.
According to its website, the purpose of the HIT Board is to:
- Establish criteria for data collection and disbursement by the statewide health information exchange and the prescription drug monitoring program to improve the quality of information provided to clinicians;
- Evaluate and ensure that the statewide health information exchange is meeting technological standards for reporting of data for the prescription drug monitoring program, including the data to be collected and reported and the frequency of data collection and disbursement;
- Provide the governance oversight necessary to ensure that any health information in the statewide health information exchange and the prescription drug monitoring program may be accessed, used, or disclosed only in accordance with the privacy and security protections set forth in HIPAA;
- Provide recommendations to the statewide health information exchange on any other matters referred to the board.
The HIT Board, sanctioned unanimously by the Nebraska legislature in 2020 to centralize health records, is now seen by some as an Orwellian instrument that poses a dramatic threat to civil liberties. The Board consists of 17 members appointed by the governor and ratified by the legislature.
Did Hear that Texas is Suing Pfizer? KAREN KINGSTON
Texas is suing Pfizer for 18 violations across 5 counts of the Texas Deceptive Trade Practices Act. Texas is petitioning for a restraining order against Pfizer and billions of dollars.
DEC 9, 2023 – Many of us have been struggling for two years on how to strike up the conversation around the damage that the COVID-19 mRNA injections have caused and continue to cause, but not knowing where to start.
The good news is that most everyone loves a good lawsuit and the Texas vs. Pfizer lawsuit does not disappoint. Maybe ask your friends or send a text, “Hey. Did you hear that Texas is Suing Pfizer?”
“Why is Texas Suing Pfizer?” Your Friend May Respond
Texas is suing Pfizer for 18 violations across 5 counts of the Texas Deceptive Trade Practices Act (DTPA). Texas is petitioning for:
- a restraining order on Pfizer to stop suppressing the truth regarding the lack of clinical benefits their mRNA injections, and
- monetary relief upwards of billions of dollars because Pfizer misrepresented the clinical outcomes of using their COVID-19 mRNA injections.
Greg Hunter and I discuss how Pfizer, and specifically the CEO Albert Bourla misrepresented the clinical outcomes of their mRNA injections. We go into detail on how Pfizer board member, Scott Gottlieb, coordinated with Twitter to silence credible scientific evidence that showed Pfizer’s COVID-19 mRNA underperformance and the serious clinical risks of their COVID-19 mRNA injections.
You can watch the full interview at USA Watchdog or on Rumble.
CDC Director Issues New Covid Alert, Urges Americans to Wear Masks (VIDEO)
Dec. 8, 2023 7:30 pm – Here we go. It must be election season!
CDC Director Dr. Mandy Cohen issued a new alert for the COVID “Pirola” variant and recommended for those who are feeling symptoms to mask up.
“Respiratory viruses commonly cause illness such as flu, COVID-19, and respiratory syncytial virus (RSV), especially in the fall and winter. There are actions you can take to protect yourself and others. Learn about how to reduce your risk of getting sick from these viruses, and if they are spreading in your community,” the CDC stated.
The CDC issued an updated COVID alert on Friday.
JN.1, a variant of the virus that causes COVID-19, is a closely related offshoot of the variant BA.2.86 that CDC has been tracking since August. JN.1 is currently projected to comprise 15-29% of circulating variants and continues to grow quickly compared with other variants. Its continued growth suggests that it is either more transmissible or better at evading our immune systems. At this time, there is no evidence that JN.1 presents an increased risk to public health relative to other currently circulating variants, and CDC is closely monitoring COVID-19 activity and JN.1 spread. The increase of this variant does not alter CDC’s COVID-19 recommendations, meaning that vaccines, tests, and treatments continue to work well against JN.1.
CDC Director Cohen said flu and RSV are cases are up.
[Ed.: The more masks, the better!]
Here We Go: CDC Issues Health Alert Over Deadly, Fast-Spreading Strain of Monkeypox By Jim Hᴏft
Dec. 9, 2023 3:20 pm – The U.S. Centers for Disease Control and Prevention (CDC) issued a health alert on Thursday to inform clinicians and health departments nationwide about the emergence and spread of a deadly subtype of the monkeypox virus, known as Clade I, predominantly in the Democratic Republic of the Congo (DRC).
This health advisory, part of the CDC’s Health Alert Network (HAN), underscores the necessity for heightened vigilance, particularly among travelers returning from the DRC. Clade I, distinguished as a distinct genetic grouping of the monkeypox virus, has not been reported in the United States to date, according to the health alert.
There is currently an outbreak of deadly monkeypox in 22 out of 26 provinces, including urban areas in Congo.
However, the possibility of its appearance in travelers necessitates increased awareness and diagnostic readiness among healthcare professionals.
Symptoms of Clade I mpox resemble those of other forms of the virus, including a widespread rash and lymphadenopathy. Clinicians are urged to promptly notify state health departments upon encountering patients exhibiting these symptoms, particularly those with recent travel history to the DRC.
The CDC also emphasizes the importance of lesion specimen submissions for clade-specific testing in such cases.
Though vaccine coverage in the U.S. is low, the CDC reasserts that vaccines such as JYNNEOS and ACAM2000 are expected to be effective against both Clade I and Clade II MPXV infections. Medical experts are urged to recommend vaccination for all eligible patients.
In a separate travel advisory, the CDC has strongly advised travelers in the Democratic Republic of the Congo (DRC) to exercise heightened caution. Key recommendations include avoiding contact with individuals who are ill, maintaining a distance from wild animals, and refraining from consuming or handling game meat.
[Ed.:
Fully Vaccinated and Boosted Piers Morgan Tests Positive for COVID-19 — Blames “Anti-Vaxx” for Catching the Virus By Jim Hᴏft
Dec. 9, 2023 10:40 am – Far-left British television personality Piers Morgan has contracted COVID-19 despite being fully vaccinated and receiving a booster shot two years ago.
The hypocritical host of “Uncensored” announced the news via Twitter, expressed his frustration, and blamed the ‘anti-vaccination’ community for his infection.
The 58-year-old host shared a photo of his positive lateral flow test on Twitter, along with a candid description of his condition: “as rough as a badger’s a***.”
[Ed.: So, a badger’s ass is a good thing? At least it’s not a ‘horse’s ass’! Words have meaning…]
Report 88: 2.5 Months After COVID Vaccine Rollout, Pfizer Changed Criteria for ‘Vaccination Failure,’ Causing 99% of Reported Cases to Not Meet That Definition. 3.9% of Reported ‘Lack of Efficacy’ Cases Ended in Death in First 90 Days of Public Vaccine Availability. by Barbara Gehrett, MD; Joseph Gehrett, MD; Chris Flowers, MD; and Loree Britt
October 11, 2023 • The War Room/DailyClout Pfizer Documents Analysis Project Post-Marketing Group (Team 1) – Barbara Gehrett, MD; Joseph Gehrett, MD; Chris Flowers, MD; and Loree Britt – penned a telling analysis of the “Vaccine Effectiveness” Safety Concern section found in Pfizer document 5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of PF-07302048 (BNT162B2) Received Through 28-FEB-2021 (a.k.a., “5.3.6“).
It is important to note that the AESIs in the 5.3.6 document were reported to Pfizer for only a 90-day period starting on December 1, 2020, the date of the United Kingdom’s public rollout of Pfizer’s COVID-19 experimental mRNA “vaccine” product.
Key highlights from this important report include:
- During the first three months of vaccine rollout, 1,665 cases were submitted to Pfizer with a definition of “lack of efficacy” (LOE).
- There were 65 deaths (3.9%) among the lack of efficacy cases.
- Lack of efficacy cases fell into two categories:
- Drug ineffective
- Vaccination failure
- Without explanation, Pfizer revised the coding conventions (or criteria) for the “vaccination failure” category on February 15, 2021, two and a half months into the vaccine’s public rollout and a mere two weeks before data collection for the report ended.
- The new definition of “vaccination failure” required all three of the following criteria to be met:
- Both doses received per local regime.
- At least seven days since the second dose.
- Infection with confirmed lab test positive for SARS-CoV-2.
- The new definition of “vaccination failure” required all three of the following criteria to be met:
- Revising the criteria for vaccination failure likely allowed Pfizer to shift cases out of the “vaccination failure” category and into “drug ineffective” category. With the new definition, 1,649 cases, or 99%, of the 1,665 lack of efficacy cases met the “drug ineffective” criteria of:
- Infection not confirmed by a lab test
- Unknowns present:
- Vaccine doses followed proper local regimen.
- Number of days since first dose.
- Whether seven days passed since second dose.
- COVID onset between 14 days after first dose and through six days after second dose.
- However, based on data in 5.3.6, only 788 (47.8%) of the 1,649 drug ineffective cases can be stated categorically not to have been drug failure.
- 1,625 (98.5%) of the 1,649 “drug ineffective” cases were labeled as “serious.”
- Using the revised coding conventions, only 16 lack of efficacy cases, under 1%, were categorized as “vaccination failure.”
- Up to another 861 cases may have been “vaccination failure” had missing data been collected.
Please read the full report below.
Canadian Journalist Who Advocated Draconian Vaxx-Passport Mandates Dies Mysteriously at 33 JD RUCKER
As always, the words “Covid” and “vaccine” are missing from every corporate media report about the untimely death.
DEC 9, 2023 – The list of outspoken Covid-19 “vaccine” advocates dying continues to grow. Most, including Canadian business journalist Ian Vandaelle, were otherwise young and healthy before their demise. Vandaelle was 33 when he died earlier this week.
As usual, nothing connecting his untimely death to Covid-19 or the spike-protein-inducing “vaccines” are openly mentioned by medical professionals or media covering the story. It doesn’t matter how many people die mysteriously. The jabs are not allowed to be considered as the root cause even though the scientific evidence makes it pretty obvious.
[Ed.: We are seeing a reduction of vaccine advocates…]
Child Mask Mandates Have No Clear Benefits and Cause Harm, BMJ Review Finds by Guy Gin
DEC 9, 2023 – A new systematic review has been published in Archives of Disease in Childhood, one of the journals of the British Medical Journal, by Sandlund et al. titled ‘Child mask mandates for COVID-19: a systematic review‘.
Since no randomised controlled trials have even been conducted on child mask-wearing or mask mandates, the authors systematically reviewed observational studies and included 22 in the final analysis: six found child mask mandates were associated with lower rates of infection; the other 16 didn’t.
But the studies that found they didn’t weren’t just greater in quantity; they were higher quality too.
Of the six studies reporting a significant negative correlation between masking and COVID-19 cases, five had critical and one had serious ROB [risk of bias]. Of the 16 studies failing to find a significant correlation, one (6.3%) had critical, 10 (62.5%) had serious, five (31.3%) had moderate and none had low ROB. [emphasis added here and below]
In short, almost all studies with critical ROB had pro-mask results, while all studies with moderate ROB did not. Table 2 below gives a breakdown of the various types of bias the reviewers found. The six studies with pro-mask results are listed first.
Exposing COVID-19 Crimes Dr. David E, Martin [1:26:23] Analysis by Dr. Joseph Mercola
The Four Felonies Exposed in 2015 Admission of COVID-19 Plot
Dive into the 2015 statement that not only admitted to the premeditated plan behind COVID-19 but also unveiled four felonies, shrouded in the guise of public health initiatives.
The video above features a lecture David E. Martin,1 Ph.D., gave in Dornach, Switzerland, in late October 2023. Martin is a national intelligence analyst and founder of IQ100 Index, which developed linguistic genomics, a platform capable of determining the intent of communications.
This technology has allowed Martin to scan and review millions of patents, resulting in a paper trail2,3 that conclusively proves SARS-CoV-2 is a manmade bioweapon that has been in the works for 58 years.
STORY AT-A-GLANCE
- In an October 2023 lecture, David E. Martin, Ph.D., detailed how we can know that SARS-CoV-2 is a manmade bioweapon that has been in the works for 58 years
- The virus called “coronavirus” was first described in 1965. Two years later, the U.S. and U.K. launched an exchange program where healthy British military personnel were infected with coronavirus pathogens from the U.S. as part of the U.S. biological weapons program
- In 1992, Ralph Baric at University of North Carolina, Chapel Hill, took a pathogen that used to infect the gut and lungs and altered it with a chimera to make it infect the heart, causing cardiomyopathy. This research was part of the efforts to produce an HIV vaccine
- In November 2000, Pfizer patented its first spike protein vaccine. Between 2000 and 2019, vaccine trials using this technology proved it was lethal, yet in the summer of 2020, the clinical trials for the SARS-CoV-2 shots went straight into human trials
- mRNA spike protein was publicly described as a bioweapon 18 years ago. In 2005, at a conference hosted by DARPA and The Mitre Corporation, the mRNA spike protein was hailed as a “biological warfare-enabling technology,” i.e., a biological warfare agent
