Please do your own research. The information I share is only a catalyst to expanding ones confined consciousness. I have NO desire for anyone to blindly believe or agree with what I share. Seek the truth for yourself and put your own puzzle together that has been presented to you. I'm not here to teach, preach or lead, but rather assist in awakening the consciousness of the collective from its temporary dormancy.
The American Medical Association (AMA) wants people to die from the Wuhan coronavirus (Covid-19).
The reason we can safely say this is that the trade group is working overtime to restrict Americans’ access to hydroxychloroquine (HCQ) and ivermectin, two safe, effective and inexpensive early treatment remedies for the Chinese Virus.
Instead of recognizing that each individual has the God-given right to choose what goes into his body, the AMA is taking a position of medical fascism that does not even recognize the right of doctors to prescribe whatever medications they see fit for their patients.
Because using ivermectin breaks the plandemic script, however – everyone is supposed to just mask up and get “vaccinated,” they tell us – the AMA is trying to make it impossible to get (except for the black market, perhaps).
“The American Medical Association (which represents only 12% of practicing physicians and receives more money from the federal government than from its waning membership dues) and two national pharmacy associations (which receive corporate support from COVID-19 ‘vaccine’ manufacturers, Pfizer, AstraZeneca and Johnson & Johnson) have decided ivermectin should not be used to treat this virus despite widespread successful treatment with this drug (discovered in the late 1970s and used in humans since 1988),” write Robert Marshall and Dr. Bernard, Pegis, M.D., for LifeSiteNews.
“Ivermectin is currently available over the counter in many countries. If American drugstores implement this dangerous policy, many lives will be lost.”
Hypocritical AMA Supported Off-Label Prescription Of Drugs As Recently As 2020
In a September 1 press release, the AMA, along with the American Pharmacists Association (APHA) and the American Society of Health-System Pharmacists (ASHP), explained that they “strongly oppose the ordering, prescribing, or dispensing of ivermectin to prevent or treat COVID-19 outside of a clinical trial.”
“We are alarmed by reports that outpatient prescribing for and dispensing of ivermectin have increased 24-fold since before the pandemic and increased exponentially over the past few months,” that announcement further read.
Even though there are almost no risks associated with taking ivermectin as normally prescribed, the AMA, the APHA and the ASHP are freaking out about the fact that some doctors are administering it to their sick patients.
Off-label prescription of pharmaceuticals has been common practice for many decades. Now that covid is here and being highly politicized by the left, however, it is suddenly a mortal sin in the eyes of the medical establishment to even just try using ivermectin for treating Chinese Germs.
Just prior to when the Fauci Flu made its appearance, the AMA actually issued an official policy guideline confirming that it offers “strong support” for the off-label prescription of pharmaceuticals whenever a doctor deems that it may be helpful.
“Our AMA confirms its strong support for the autonomous clinical decision-making authority of a physician and that a physician may lawfully use an FDA approved drug product or medical device for an off-label indication when such use is based upon sound scientific evidence or sound medical opinion,” the organization confirmed at the time.
Now that the Biden regime wants everyone to get “vaccinated,” though, the AMA is doing everything possible to restrict access to ivermectin, which quite frankly would have put an end to this fake “pandemic” a long, long time ago.
“Jesus was severely criticized for healing a blind man on the Sabbath (John 9:13-30),” LifeSiteNews reported.
“Today, practicing physicians who save lives using drug therapy are ostracized. Mainstream medicine appears to be rejecting efforts to combat COVID-19 with drugs in favor of experimental mRNA ‘vaccines.’”
The Pfizer Covid-19 injection has been given emergency use authorisation to be used in children over the age of 12 in the UK by the MHRA, whilst the Joint Committee on Vaccination and Immunisation (JCVI) have decided that vulnerable children over the age of 12 and all 16 and 17 year olds should be offered the Pfizer jab. Both authorities claim that their decision is based on the benefits outweighing any potential risks.
If this is the case, then the MHRA and JCVI need to explain how they came to this conclusion when just 1 in every 1.7 million children have died with Covid-19 in 18 months, whilst 1 in every 9 children suffered a serious adverse reaction to the Pfizer vaccine in the small and short clinical trial which left them unable to perform daily activities.
According to official NHS data published weekly, between March 2020 and the 11th August 2021 a total of 3,743 people have died with Covid-19 in UK hospitals who had no underlying conditions, whilst 85,410 have allegedly died with Covid-19 who had other serious underlying conditions.
These conditions include ailments such as chronic kidney disease, chronic neurological disease, chronic pulmonary disease, heart disease, and dementia.
However, the vast majority of these deaths have occured in people over the age of 80, and people between the age of 60 and 79; the vast majority of which are closer to the age of 79.
The number given by the NHS of people who have died with Covid-19 since March 2020, between the ages of 0 and 19, who had underlying conditions is just 38.
Whilst the people who have died with Covid-19 snce March 2020, between the ages of 0 and 19, who had no other known underlying conditions stands at just 9.
Whilst just 1 in every 1.7 million children have allegedly with Covid-19 in 18 months, who had no know pre-existing conditions.
Every death is of course a tragedy, especially when it is somebody so young, but we need to put these numbers into context now that an experimental injection is going to be given to children in the United Kingdom in the name of protecting them from Covid-19.
During the clinical trial to test the efficacy and safety of the Pfizer Covid-19 vaccine in children aged 12 and over, 1,127 children were given one dose of the mRNA jab, but only 1,097 children received the second dose. This fact in itself raises questions as to why 30 children did not receive a second dose of the Pfizer jab.
Of the 1,127 children who received a first dose of the jab a shocking 86% experienced an adverse reaction. Of the 1,097 children who received a second dose of the jab a shocking 78.9% experienced an adverse reaction.
Of course these adverse reactions include things such as a sore arm, so therefore it is vital to know the rate of serious adverse reactions that occurred during the limited clinical trial.
For children 12 to 15 years of age, the Pfizer COVID-19 vaccine clinical trial found the overall incidence of severe adverse events which left them unable to perform daily activities, during the two-month observation period to be 10.7%, or 1 in 9, in the vaccinated group and 1.9% in the unvaccinated group, resulting in a vaccine risk of 8.8% or 1 in 11 vaccinated children.
Consequently, children who received the vaccine had nearly six times the risk of a severe adverse event occurring in the two-month observation period compared to children who did not receive the vaccine.
In addition, the incidence of Covid-19 in the unvaccinated group was 1.6%, therefore, there were almost seven times more severe adverse events observed in the vaccinated group than there were Covid-19 cases in the unvaccinated group.
As you can clearly see based on the number of children to have allegedly died with Covid-19 in 18 months, and the number of children to have suffered a serious adverse reaction in the clinical trial, the benefits of giving children the Covid-19 injection do not outweight the risks.
But there may be some who naively believe children should be given the injection because it will help to prevent transmission of the Covid-19 virus, but that is not what these experimental injections do.
The Pfizer clinical trial was not designed to observe asymptomatic infection with SARS-CoV-2 or the effect of the vaccine on the spread (transmission) of COVID-19. Consequently, the FDA states that “it is possible that asymptomatic infections may not be prevented as effectively as symptomatic infections” and “data are limited to assess the effect of the vaccine against transmission of SARS-CoV-2 from individuals who are infected despite vaccination.”
This is also proven by the fact thousands of fully vaccinated individuals are allegedly testing positive for Covid-19, being hospitalised and dying. The latest Public Health England report shows that fully vaccinated individuals account for 65% of all alleged Covid-19 deaths since February 2021.
Therefore due to the fact the Covid-19 vaccines do not prevent infection or transmission, 1 in every 9 children suffered a serious adverse reaction leaving them unable to perform daily activities during the clinical trial, and just 1 in every 1.7 million children having allegedly died with Covid-19 in 18 months, how on earth can the MHRA and JCVI justify giving the Covid-19 vaccine to children and claim that their decision is based on the potential benefits outweighing any risks?
There is a sequence of outright lies and fabrications used to justify far-reaching policy decisions which in the course of the last 18 months are literally destroying people’s lives Worldwide.
“Fake science” is used to justify confinement, social distancing, the face mask, the prohibition of social gatherings, cultural and sports events, the closure of economic activity, all of which are upheld as a means to repealing the “killer virus”.
Who is this “Killer Virus” which has been personified by both the media and our governments, held responsible for triggering economic and social chaos Worldwide?
You might recall that at the height of the February 2020 financial collapse, “V the Virus” was held responsible for the largest stock market crash since 1929.
Has the “Killer Virus” been Identified. Has SARS-CoV-2 been Isolated?
This article will review this contentious issue starting at the outset of the crisis in January 2020. Part of this analysis is based on research conducted in early 2020.
The central question raised in this review is the following: is there reliable evidence provided by the WHO and national health authorities that the alleged SARS-CoV-2 virus has been isolated/purified from an “unadulterated sample taken from a diseased patient”?
While the alleged virus was initially defined as the 2019 novel coronavirus (2019-nCoV) in January 2020, the World Health Organization (WHO) stated in January 2020 that it did not have in its possession details regarding the isolation/purification and identity of 2019-nCoV.
And because details concerning isolation / purification were not available, the WHO decided to “customize” The Real Time Reverse Transcription Polymerase Chain Reaction (rRT-PCR) Test using the alleged “similar” 2003 SARS virus (subsequently renamed SARS-1) as “a point of reference” for detecting genetic fragments of the novel 2019-nCoV.
What this decision entails is that novel 2019-CoV-2 is NOT a novel virus. It was categorized by the Chinese authorities and the WHO as “similar” to the 2003 SARS-CoV as well as to MERS.
2003 SARS-CoV was subsequently renamed SARS-CoV-1.
History: Isolation of the Virus
Chinese Health Authorities
The Chinese authorities announced on January 7, 2020 that “a new type of virus” had been identified “similar to the one associated with SARS and MERS” (related report , not original Chinese government source). The underlying method is described below:
We prospectively collected and analysed data on patients with laboratory-confirmed 2019-nCoV infection by real-time RT-PCR and next-generation sequencing.
Data were obtained with standardised data collection forms shared by WHO and the International Severe Acute Respiratory and Emerging Infection Consortium from electronic medical records. (emphasis added)
The following article entitled “A new coronavirus associated with human respiratory disease in China, (Nature, February 3, 2021) was among the first to report on the China’s novel coronavirus:…[We] collected bronchoalveolar lavage fluid (BALF) and performed deep meta-transcriptomic sequencing. The clinical specimen was handled in a biosafety level 3 laboratory at Shanghai Public Health Clinical Center. Total RNA was extracted from 200 μl of BALF and a meta-transcriptomic library was constructed for pair-end (150-bp reads) sequencing using an Illumina MiniSeq as previously described 4,6,7,8. .In total, we generated 56,565,928 sequence reads that were de novo-assembled and screened for potential aetiological agents. ….The genome sequence of this virus, as well as its termini, were determined and confirmed by reverse-transcription PCR (RT–PCR)10 and 5′/3′ rapid amplification of cDNA ends (RACE), respectively. This virus strain was designated as WH-Human 1 coronavirus (WHCV) (and has also been referred to as ‘2019-nCoV’) and its whole genome sequence (29,903 nt) has been assigned GenBank accession number MN908947. .The viral genome organization of WHCV was determined by sequence alignment to two representative members of the genus Betacoronavirus: a coronavirus associated with humans (SARS-CoV Tor2, GenBank accession number AY274119)  and a coronavirus associated with bats (bat SL-CoVZC45, GenBank accession number MG772933) . (Nature, February 3, 2020) .
It is unclear from the above quotations as well as from the documents consulted, whether the Chinese health authorities undertook an isolation / purification of a patient’s specimen.
US Centre for Disease Control and Prevention (CDC)
Following the Chinese announcement on the 28th of January 2020, the US Centre for Disease Control and Prevention (CDC) stated that the novela corona virus had been isolated.The CDC statement dated January 28th, 2020 (updated December 2020) is unequivocal:
SARS-CoV-2, the virus that causes COVID-19, was isolated in the laboratory and is available for research by the scientific and medical community.
On January 20, 2020, CDC received a clinical specimen collected from the first reported U.S. patient infected with SARS-CoV-2. CDC immediately placed the specimen into cell culture to grow a sufficient amount of virus for study.
On February 2, 2020, CDC generated enough SARS-CoV-2 grown in cell culture to distribute to medical and scientific researchers.
On February 4, 2020, CDC shipped SARS-CoV-2 to the BEI Resources Repository.
An article discussing the isolation and characterization of this virus specimen is available in Emerging Infectious Diseases.
One important way that CDC has supported global efforts to study and learn about SARS-CoV-2 in the laboratory was by growing the virus in cell culture and ensuring that it was widely available. Researchers in the scientific and medical community can use virus obtained from this work in their studies.
SARS-CoV-2 strains supplied by CDC and other researchers can be requested, free, from the Biodefense and Emerging Infections Research (BEI) Resources Repositoryexternal icon by established institutions that meet BEI requirements. These requirements include maintaining appropriate facilities and safety programs, as well as having the appropriate expertise. BEI supplies organisms and reagents to the broader community of microbiology and infectious disease researchers. (Emphasis added).
See also related study which was posted on the CDC website.
The CDC Acknowledges that SARS-CoV-2 has not been Isolated.
The official CDC document, (dated July 21, 2021) entitled “CDC 2019-Novel Coronavirus (2019-nCoV) Real-Time RT-PCR Diagnostic Panel reads as follows:
Since no quantified virus isolates of the 2019-nCoV were available for CDC use at the time the test was developed [January 2020] and this study conducted, assays designed for detection of the 2019-nCoV RNA were tested with characterized stocks of in vitro transcribed full length RNA (N gene; GenBank accession: MN908947.2) of known titer (RNA copies/µL) spiked into a diluent consisting of a suspension of human A549 cells and viral transport medium (VTM) to mimic clinical specimen. (emphasis added, page 40)
Compare the above statement to the CDC January 28th, 2020 advisory confirming the isolation of SARS-CoV-2:
On January 20, 2020, CDC received a clinical specimen collected from the first reported U.S. patient infected with SARS-CoV-2. CDC immediately placed the specimen into cell culture to grow a sufficient amount of virus for study.
See the analysis of CDC responses in the section below on Freedom of Information Requests.
The World Health Organization (WHO) Did Not Undertake The Isolation / Purification of a Specimen
From the documents quoted below, the Chinese authorities did not provide the WHO with a specimen ofisolated / purified SARS-CoV-2.
And because details concerning isolation were not available, the WHO decided to “customize” its Real Time Reverse Transcription Polymerase Chain Reaction (rRT-PCR) test using a so-called isolate of the “similar” 2003 SARS corona virus (subsequently renamed SARS-CoV-1) as “a point of reference” (or proxy) for detecting genetic fragments of the 2019 SARS-CoV-2.
While Drosten et al’s study confirmed that “several viral genome sequences had been released”, in the case of 2019-nCoV, “virus isolates or samples from infected patients were not available … ”
The recommendations to the WHO were as follows:
“The genome sequences suggest presence of a virus closely related to the members of a viral species termed severe acute respiratory syndrome (SARS)-related CoV,a species defined by the agent of the 2002/03 outbreak of SARS in humans [3,4].
We report on the the establishment and validation of a diagnostic workflow for 2019-nCoV screening and specific confirmation [using the RT-PCR test], designed in absence of available virus isolates or original patient specimens. Design and validation were enabled by the close genetic relatedness to the 2003 SARS-CoV, and aided by the use of synthetic nucleic acid technology.” (Eurosurveillance, January 23, 2020, emphasis added).
What this bold statement suggests is that the isolation / purification of 2019-nCoV was not required and that “validation” would be enabled by “the close genetic relatedness to the 2003-SARS-CoV.”
The investigative report provides detailed documentation based on Freedom of Information (FOI) requests addressed to ninety Health /Science institutions in a large number of countries.
The responses to these requests confirm that there is no record of isolation / purification of SARS-CoV-2 “having been performed by anyone, anywhere, ever.”
“The 90 Health /Science institutions that have responded thus far have provided and/or cited, in total, zero such records:
Our requests [under “freedom of information”] have not been limited to records of isolation performed by the respective institution, or limited to records authored by the respective institution, rather they were open to any records describing “COVID-19 virus” (aka “SARS-COV-2”) isolation/purification performed by anyone, ever, anywhere on the planet.”
The Centre for Disease Control and Prevention (CDC)
The CDC was contacted by the author of this report in the form of four separate requests: November 2, 2020, March 1, 2021, March 3, 2021, which are reviewed below:
March 1, 2021:The CDC again made clear that they still have no records of “SARS-COV-2” isolation performed by anyone, anywhere on the planet, ever… just not in so many words. Instead, the CDC absurdly implied that isolation/purification of “SARS-COV-2” would require the replication of a “virus” without host cells and thus is impossible. (The request had nothing to do with replication.)
CDC again failed to provide/cite any records describing “SARS-COV-2” isolation/purification by anyone anywhere ever… but would no longer simply say so (as they did on November 2nd); instead they gave song and dance citing the study by Harcourt et al. which is the same one posted on CDC’s website:
Here are 5 compilation pdfs containing FOI responses from 79 institutions in 22 countries/jurisdictions, re the isolation/purification/existence of “SARS-COV-2”, as well as emails from authors of studies that claimed to have “isolated the virus” and an email from the Head of the Consultant Laboratory for Diagnostic Electron Microscopy of Infectious Pathogens at Germany’s Robert Koch Institut, last updated July 13, 2021
Screenshot of a selected responses are provided below : New Zealand, Canada, UK.
Consult the full archive of letters and responses. This work was undertaken over a period of more than 12 months.
“Gemma O’Doherty is an Investigative Journalist in Ireland.
“This Irish Investigation into Covid shows that The Department of Health refuses to confirm the existence of a “virus” in writing. Confirmation that the virus was never isolated.”
“As part of our legal action we had been demanding the evidence that this virus actually exists [as well as] evidence that lock downs actually have any impact on the spread of viruses; that face-masks are safe, and do deter the spread of viruses – They don’t. No such studies exist; that social distancing is based in science – It isn’t. it’s made up; that contact tracing has any bearing on the spread of a virus – of course it doesn’t. This organization here – is making it up as they go along.” – Gemma O’Doherty
Isolation of the Virus. The Legal Battle in Alberta. Patrick King
Patrick King. The Virus Has Not Been Isolated! “No I Did Not Win The Court Case”. “They Do Not Have the Evidence”.
The following video features Patrick King in his legal Battle against the Alberta Government. There are a lot of people in Alberta and around the World who are Fighting against the Big Lie.
Concluding Remarks: “Biggest Medical Fraud in World History”
SARS-CoV-2 has not been isolated. Does the virus Exist?
Neither the Chinese authorities nor the CDC, the WHO, national governments, scientific / health authorities have provided evidence that SARS-CoV-2 has been isolated /purified.
Based on the investigative research of Christine Malley we have access to the responses of numerous governments and health authorities, including that provided by the Republic of Ireland to journalist Gemma O’Doherty.
What this means is that the entire covid narrative falls flat.
We have been systematically misled.
Everything you have been told by your governments is a lie, a complexity of lies and falsehoods.
There is no pandemic. The isolation / purification of the virus has not been undertaken.
All the policies adopted by governments worldwide allegedly to “save lives” are illegal, socially destructive and in violation of fundamental human rights.
These policies have been instrumental in “destroying people’s lives”.
Dr. Stephen Frost refers to the alleged “Covid pandemic” as“The Biggest Medical Fraud in World History”.
From the outset in January 2020, the flawed and invalid RT-PCR test was used to “detect” the alleged 2019 SARS-CoV-2 virus, despite the fact that details regarding the isolation/purification of the original virus were not available.
Curbing the alleged SARS-CoV-2 pandemic through the imposition of face masks, social distancing, closing down of national economies are of a criminal nature, they have absolutely no validity,
The original strain of SARS-CoV-2 has not be isolated /purified: How does that affect the process of so-called “detection” of the “deadly variants” of the original virus?
Mortality and Morbidity: While there is “No Killer Virus”, there is a “Killer Vaccine”.
While the SARS-CoV-2 virus is presented by the media and the governments as a “killer virus” (when in fact the WHO and CDC describe it as “similar to seasonal influenza”, a totally invalid and dysfunctional Covid -19 vaccine is currently being imposed on the entire population of Planet Earth: 7.9 billion people.
It’s a multibillion dollar endeavour with Pfizer in the lead, establishing a near Worldwide monopoly for the sale and distribution of the mRNA killer vaccine.
How did Big Pharma manage to develop a vaccine (sponsored by the WHO, GAVI, the Gates Foundation, et al) with a mandate “to protect people” against a virus which has not been isolated/ purified?
Moreover, 2019SARS-CoV-2 has been categorized as similar to the 2003 SARS-CoV which means that the 2019 SARS-CoV-2 is not a novel virus.
The legitimacy of the Covid vaccine project hinges upon the hundreds of thousands of RT-PCR fake positive cases Worldwide combined with fake Covid related mortality data.
Big Pharma’s mRNA vaccine has resulted in countless deaths and injuries Worldwide which are barely reported by the mainstream media.
While we do not have figures for the entire Planet, the latest official figures for the European Union and the U.S are revealing. Bear in mind they vastly underestimate the real trends in vaccin related mortality and morbidity:EU/EEA/Switzerland to 31 July 2021 – 20,595 Covid-19 injection related deaths and over 1.94 million injuries, per EudraVigilance Database.
UK to 21 July 2021 – 1,517 Covid-19 injection related deaths and over 1.1 million injuries, per MHRA Yellow Card Scheme.
USA to 23 July 2021 – 11,940 Covid-19 injection related deaths and over 2.4 million injuries, per VAERS database.
TOTAL for EU/UK/USA – 34,052 Covid-19 injection related deaths and over 5.46 million injuries reported as at 1 August 2021
Nota Bene: It is important to be aware that the official figures above (reported to the health authorities) are but a small percentage of the actual figures. Furthermore, people continue to die (and suffer injury) from the injections with every day which passes. (D4CE
So why are governments pressuring people to get vaccinated?
Heads of State and heads of government Worldwide are being pressured, bribed, coopted and/or threatened by powerful financial interests into accepting the Covid vaccine consensus. The vaccine passport is the endgame, which constitutes a transition towards digital tyranny.
The study and reports analyzed in this article should be used to confront politicians.
Does the virus Exist?
The governments and the WHO do not have a Leg to Stand On. And neither does Bill Gates.
What we must seek is to confront a very fragile consensus, which is based on fraud and deceit.
PS: I remain indebted to Christine Massey for her extensive research and investigation on the issue of isolation /purification.
Rebeca Cruz-Esteves at Jefferson Abington, where she’s been hospitalized in the neurology unit for the past week. (Courtesy of Rebeca Cruz-Esteves)
This admission was recorded during the June 22, 2021 episode of The Stew Peters Show by the independent conservative reporter and political commentator Stew Peters.
During that day’s episode, Peters played an audio recording made by a woman who developed Guillain-Barre syndrome after receiving the Moderna vaccine.
Guillain-Barre syndrome is an autoimmune disorder. It causes the body’s immune system to attack its own nerves. Its first symptoms include weakness and a tingling sensation in the extremities.
This then rapidly spreads and eventually leads to whole-body paralysis. The woman’s doctor believes she got Guillain-Barre from the coronavirus vaccine.
The woman’s physician, a neurologist, filed an adverse event report with the Vaccine Adverse Events Reporting System. But the woman decided this was not enough and wanted to take it up with Moderna.
She called the company and spoke with a representative who was not surprised to hear about her injury.
During the call, the Moderna representative read her a disclaimer:
“The Moderna COVID-19 vaccine has not been approved or licensed by the Food and Drug Administration, but it has been authorized for emergency use by the FDA under an emergency use authorization to prevent coronavirus disease 2019, for use in individuals 18 years of age and older.”
“There is no FDA-approved vaccine to prevent COVID-19. The EUA for the Moderna COVID-19 vaccine is in effect for the duration of the COVID-19 EUA declaration, justifying emergency use of the product unless that declaration is terminated or the authorization is revoked sooner.”
In addition to this admission that the vaccines are experimental, the Moderna representative pointed out that all of its clinical trial phases are still ongoing and that the company still does not know the vaccine’s long-term protective efficacy.
When the woman asked the representative if everybody who gets Moderna’s vaccine is a part of the company’s clinical trial, the spokesperson replied, “pretty much, yeah.”
This means that millions of people all over the world are guinea pigs in a clinical trial that they have not specifically signed up to participate in.
Other Coronavirus Vaccines Causing People To Develop Guillain-Barre Syndrome
Less than 15 minutes after she received her dose, she experienced an anaphylactic reaction to the vaccine. Over the next few days, her symptoms progressed. She started experiencing muscle spasms, twitches and stiffness in her legs and biceps. She experienced memory fog, declining eyesight in one eye and a whole host of other neurological symptoms. Eventually, she was diagnosed with Guillain-Barre.
Cruz-Esteves’ story shows that the woman on Peters’ program is not unique. Worse yet, it shows that this situation is not limited to Moderna’s vaccines.
In fact, the FDA has already acknowledged 100 cases of Guillain-Barre syndrome associated with the Johnson & Johnson COVID-19 vaccine.
The Centers for Disease Control and Prevention (CDC) also admitted that the vaccines can cause Guillain-Barre syndrome. But in the agency’s statement, the CDC claimed the reports were “rare” but indicated that the syndrome is a side effect of the vaccine.
“These cases have largely been reported about two weeks after vaccination and mostly in males, many aged 50 years and older,” added the CDC.
According to the FDA’s own data on the matter, 95 of the 100 cases resulted in hospitalization and at least one person died.
This is the second time that the Johnson & Johnson vaccine has been linked to dangerous side effects. Back in April, health officials temporarily halted the use of the vaccine after dozens of women developed blood clots after receiving the vaccine. At least three of the cases were fatal.
In a factory that produces products, there are mechanisms and machines that churn out those products, and their functioning mechanisms can be controlled, of course, as to how many are produced, how quickly, and when that production line needs to be shut off or shut down.
Sometimes supply exceeds demand, so there’s no more need to create the product (at least temporarily), or sometimes the products are defective, and the machines must be shut down until the problem is resolved.
There are “mechanisms” in our human cells that function in a similar way, controlling quality, quantity and frequency of production, until they are broken or hacked by cancer cells or… wait for it… mRNA vaccine technology.
Let’s take a look at the uncontrolled cell division in cancer cells that’s strikingly similar to the ongoing vaccine situation where human cells are now instructed by mRNA to keep creating toxins in the human body, without any “controls” or “mechanisms” in place to shut down that production.
In other words, mRNA manipulates human cells to create antigens your other cells recognize as viral invaders (pathogens) of the body.
People with a weak or “compromised” immune system are easily overwhelmed by this constant and growing invasion created from the “dose” of mRNA, about 100 to 200 micrograms, that produce several billion protein particles.
These protein particles do not replicate like cancer cells, but they are being created uncontrollably by your own cells, so even though they don’t divide, replicate and multiply, they are being produced relentlessly, like a factory, and nobody can seem to answer the question of when they stop producing.
Nobody knows how long the mRNA keeps telling your cells to produce more spike protein, and plausibly, it could be many months or even years. Is that enough to kill healthy people too?
Cancer Is The By-Product Of Broken DNA Replication, And Blood Clots Caused By MRNA Vaccines Are The By-Product Of An Overload Of Abnormal Protein Production
In both situations, the human cells have lost control of production, and the codes have been rewritten (like a bioweapon) to produce toxins the human body rejects. That’s where the “loss of control” begins, and that’s where cancer begins.
Now you can begin to rationalize the danger of getting injected with mRNA “technology” that becomes your new “factory manager” who has reprogrammed your body to become its own enemy.
Forced DNA/RNA code changes from the mRNA vaccines instruct human cells to create unlimited amounts of proteins and prions. The body is now a big waste dump for pathogenic “proteins” that just keep “showing up.” This is what is leading to all these blood clot cases and inflamed hearts we’re reading and hearing about all around the world, from every nation.
This is why they should NOT have been allowed to skip clinical trials on all these Covid-19 vaccines. This is why they were only granted EMERGENCY approval (EUA) which only makes all this one huge “medical experiment.”
Forced Code Changes At The DNA/RNA Level Have No Mechanism Of Control Or “Shut Off” Switch
More than a hundred hospital employees and supporters gathered in protest of the firing of employees who reject COVID-19 shots.
Houston – On Monday afternoon, employees of the Houston Methodist hospital system were joined by supporters from around the Houston area as they were suspended without pay for saying no to COVID-19 injections. The employees are now suing Houston Methodist in an effort to fight against COVID19 mandates.
The Houston Methodist hospital operates eight hospitals with more than 26,000 employees. On March 31, Methodist CEO Dr. Marc Boom announced that the shots – which have not received approval by the US Food and Drug Administration – would be mandatory for all employees. Houston Methodist hospital employees were told to take the shots by June 7th or lose their jobs. Methodist also required hospital managers to have at least one COVID shot by April 15th. Those who chose not to receive the treatments by Monday now have 2 final weeks before they will officially be fired.
“Mandating the vaccine was not a decision we made lightly. … Because science has proven that the Covid-19 vaccines are not only safe, but extremely effective, it became an easier decision to make,” Boom wrote in a letter to staff in April.
Jennifer Bridges is one of the nurses leading the charge. In recent months she has become the public face of the hospital employees’ fight against mandates they see as unconstitutional. On Monday evening, Bridges walked out of the Baytown Methodist hospital to a crowd of cheering supporters. “I am sad, I am happy, I am proud,” Jennifer said as she exited the parking lot for the final time.
Bridges stated that the hospital attempted to “bribe” employees with cash and required those receiving the injection to sign a waiver stating they would not hold Methodist hospital liable if they were to experience an adverse reaction. She says that nurses who treated COVID-19 patients in 2020 are now treating patients who have had reactions to the shots.
“We’ve already had nurses who took the vaccine – whether they wanted to or were forced – and so many have come down with adverse reactions. I’ve already heard from nurses who have had miscarriages,” Bridges stated during an interview with Free Thinker Radio.
Bridges was joined by nurses and doctors from the Houston area, including fellow employees from the various Houston Methodist campuses. One such Methodist nurse was Lacey Guedry. “I don’t think a mandated vaccine is ethical. At the very least I think it violates our basic liberties and freedoms, especially with institutions claiming to be practicing evidence based medicine,” said Guedry. “The WHO recently went on record saying that natural infection provides superior or equal protection that the vaccine does. So if we are going to follow “science” why are we neglecting this information?”
Although the lawsuit was filed in Texas state court it was recently transferred to a Houston federal court, a move that has been called unusual by the plaintiffs attorneys. On Friday, U.S. District Judge Lynn Hughes denied a temporary restraining order which would have prevented the Houston hospital system from firing the employees until the case is worked out.“The plaintiffs are not just jeopardizing their own health; they are jeopardizing the health of doctors, nurses, support staff, patients and their families,” Hughes wrote.
Courthouse News reports that Judge Hughes “appears ready to dispose of the lawsuit” after he authorized Houston Methodist to file a motion to dismiss the lawsuit. A hearing is scheduled for Friday June 11.
In the lawsuit Bridges and the other plaintiffs argue that, “There were 4,434 death reports and over 12,619 serious injuries reported to the CDC’s VAERS [Vaccine Adverse Event Reporting System] database from Covid-19 vaccines through May 10, 2021”, which has since risen to 5,165 deaths and 25,359 serious injuries through May 28, 2021. The plaintiffs argue that they are protected by a 1985 Texas Supreme Court decision in the case Sabine Pilot Service Inc. v. Hauck. In that case the court found that employees could sue if the only reason they were fired was for refusing to do an illegal act. They also argue that the hospitals mandate violates federal laws on authorizing medical products in emergencies.
Bridges and the other plaintiffs accuse Houston Methodist of arbitrarily denying vaccine exemption requests, despite having a policy for medical and religious exemptions. “Methodist claims that they offer religious and medical exemptions, but it (the exemption request) goes against a panel of judges and they have denied 80-85% of them,” she stated.
I spoke with a nurse at Houston Methodist whose medical exemption was approved who supported the employees right to say no to the shots. “I’m here to show support for my fellow Methodist employees who were not allowed a choice in their medical care. They were bullied and bribed into taking a vaccine,” she said on Monday afternoon. “Luckily they approved my exemption, but there have been many, many which have not been approved.”
One of the nurses who had her exemption request denied was Melissa Smith of the Clear Lake Methodist Hospital.
“Friday was my last day. Tomorrow I will sign my suspension and then they will give me 2 weeks to take the J & J vaccine. I am not going to get the vaccine and they will fire me,” Smith told TLAV. She applied for a religious exemption from the treatment and was denied. “This was under our Director of the Operating Room and the manager of my department. They gave us specific instructions on how to fill out the exemption form. So many of us did and all were denied. We all received the blanket email. I actually believe no one even read it.”
Smith estimated that the number of nurses at her hospital requesting religious exemption was in the 40’s.
“I am really here for the people who have cried, the people I have prayed with who got vaccinated because they felt they didn’t have a choice,” Smith stated while the crowd of supporters gathered outside the Baytown Methodist Hospital. “They didn’t have a voice, they felt they had nowhere to go. I am hoping that this kind of action gives them that voice and gives us choices.”
This is all openly admitted by the FDA, which has published extremely disturbing reports of adverse reactions experienced by children in a Pfizer covid vaccine “fact sheet” labeled 144413. See the original FDA document here (PDF).
FDA Admits MRNA Vaccines Cause Adverse Reactions In 86% Of Children, But Calls It “Safe” Anyway
This Pfizer page at the FDA provides links to all the fact sheets and press releases where the FDA celebrates expanding its emergency use authorization to children aged 12 to 15.
That fact sheet contains the following table that details the alarming rate of side effects and damage experienced by 12 – 15 year olds (i.e. children) who were given the mRNA injections:
Table 5: Study 2 – Frequency and Percentages of Adolescents With Solicited Local Reactions, by Maximum Severity, Within 7 Days After Each Dose – Adolescents 12 Through 15 Years of Age.
As you can see from the table, 1127 children were given the first dose of the vaccine, and 1097 children received the second dose. What happened to the 30 children who didn’t show up for the second dose? Did they die? Why were they removed from the second dose?
Among those children injected with the mRNA vaccine medical experiment:
A shocking 86% experienced side effects.
Nearly 44% suffered “moderate” side effects defined as “interfering with activity.”
66% of the children experienced fever.
65% suffered headaches.
Other side effects experienced by these children as part of these medical experiments include chills, vomiting, diarrhea, fever, muscle pain and even joint pain.
Even after 86% of children experienced such side effects after being injected with the first dose, researchers continued to inject the children with a second dose.
The FDA Claims This Is All About “Protecting” Children While Pushing More Vaccine Sales To Generate Billions Of Dollars In Profits For Pfizer
The FDA claims in its celebratory press release that expanding Pfizer’s experimental vaccine to 12 to 15-year-olds is a kind of breakthrough, not a crime against children:
“The FDA’s expansion of the emergency use authorization for the Pfizer-BioNTech COVID-19 Vaccine to include adolescents 12 through 15 years of age is a significant step in the fight against the COVID-19 pandemic,” said Acting FDA Commissioner Janet Woodcock, M.D..
“Today’s action allows for a younger population to be protected from COVID-19, bringing us closer to returning to a sense of normalcy and to ending the pandemic. Parents and guardians can rest assured that the agency undertook a rigorous and thorough review of all available data, as we have with all of our COVID-19 vaccine emergency use authorizations.”
In other words, the FDA is admitting they are fully aware of the 86% side effect ratewhen it comes to injecting children with experimental mRNA “vaccines.”
Vaccine Medical Experiments Are Harming Children In The Name Of Big Pharma Profits
When it comes to mRNA vaccine trials in the USA, when serious reactions such as facial paralysis are identified in the vaccinated group, the FDA (and presumably, the researchers) dismiss them as coincidence. From the FDA’s own document:
Bell’s palsy (facial paralysis) was reported by four participants in the Pfizer-BioNTech COVID-19 Vaccine group. Onset of facial paralysis was Day 37 after Dose 1 (participant did not receive Dose 2) and Days 3, 9, and 48 after Dose 2. No cases of Bell’s palsy were reported in the placebo group. Currently available information is insufficient to determine a causal relationship with the vaccine.
Thus, no matter what horrific side effects are caused by the vaccine experiment, they are dismissed and ignored. After all, there are billions of dollars to be earned from authorizing vaccines for widespread use in children. (It’s a whole new demographic market to target.)
This FDA document even admits the vaccine is not approved and may cause serious injury or even death:
FDA has authorized the emergency use of the Pfizer-BioNTech COVID-19 Vaccine, which is not an FDA-approved vaccine.
Adverse Reactions in Clinical Trials
Adverse reactions following the Pfizer-BioNTech COVID-19 Vaccine that have been reported in clinical trials include injection site pain, fatigue, headache, muscle pain, chills, joint pain, fever, injection site swelling, injection site redness, nausea, malaise, and lymphadenopathy (see Full EUA Prescribing Information).
Adverse Reactions in Post Authorization Experience
Severe allergic reactions, including anaphylaxis, and other hypersensitivity reactions (e.g., rash, pruritus, urticaria, angioedema), diarrhea, vomiting, and pain in extremity (arm) have been reported following administration of the Pfizer-BioNTech COVID-19 Vaccine outside of clinical trials. Additional adverse reactions, some of which may be serious, may become apparent with more widespread use of the Pfizer-BioNTech COVID-19 Vaccine.
The FDA also admits that life-threatening anaphylactic shock may occur following the vaccine, or that vaccine recipients may lose consciousness:
Appropriate medical treatment used to manage immediate allergic reactions must be immediately available in the event an acute anaphylactic reaction occurs following administration of Pfizer-BioNTech COVID-19 Vaccine.
Syncope (fainting) may occur in association with administration of injectable vaccines, in particular in adolescents. Procedures should be in place to avoid injury from fainting.
Fuellmich and his team present the incorrect PCR test and the order for doctors to describe any comorbidity death as a Covid death – as fraud.
The PCR test was never designed to detect pathogens and is almost 100% inaccurate at 35 cycles. All PCR tests monitored by the CDC are set at 37 to 45 cycles. The CDC acknowledges that tests over 28 cycles are not allowed for a positive reliable result.
This invalidates over 90% of the alleged Covid cases / “infections” detected by the use of this incorrect test.
In addition to the incorrect tests and fraudulent death certificates, the “experimental” vaccine itself violates Article 32 of the Geneva Convention.
Under Article 32 of the 1949 Geneva Convention, “mutilation and medical or scientific experiments not required for the medical treatment of a protected person” are prohibited.
According to Article 147, conducting biological experiments on protected persons is a serious breach of the Convention.
The “Experimental” Vaccine Violates All 10 Nuremberg Codes – Which Carry The Death Penalty For Those Who Try To Break These International Laws:
1) Provides immunity to the virus
This is a “leaky” gene therapy that does not provide immunity to Covid and claims that they reduce the symptoms, but double-vaccinated are now 60% of patients who need ER or ICU with covid infections.
2) Protects the recipients from getting the virus
This gene therapy does not provide immunity and the double vaccine can still catch and spread the virus.
3) Reduces deaths due to viral infection
This gene therapy does not reduce deaths from the infection. Double-vaccinated people infected with Covid have also died.
4) Reduces the circulation of the virus
This gene therapy still allows the virus to spread because it gives zero immunity to the virus.
5) Reduces the transmission of the virus
This gene therapy still allows transmission of the virus because it does not confer immunity to the virus.
The following violations of the Nuremberg Code apply:
Nuremberg Code # 1: Voluntary consent is important
No person should be forced to take a medical experiment without informed consent.
Many media, political and non-medical people urge people to take the injection.
They do not provide information about the negative effects or dangers of this gene therapy. All you hear from them is – “safe and effective” and “the benefits outweigh the risks.”
Countries use blockades, coercion and threats to force people to take this vaccine or are banned from participating in free society under the mandate of a vaccine pass or Green Pass.
During the Nuremberg trials, the media were also prosecuted and members were killed for lying to the public, along with many of the doctors and Nazis found guilty of crimes against humanity.
Nuremberg Code # 2: Yields with fruitful results that cannot be produced by other means
As mentioned above, gene therapy does not meet the criteria for a vaccine and does not offer immunity to the virus. There are other medical treatments that give fruitful results against Covid, such as Ivermectin, vitamin D, vitamin C, zinc and strengthened immune system for flu and colds.
Nuremberg Code # 3: Basic experiments as a result of animal experiments and natural history disease
This gene therapy skipped animal experiments and went directly to human experiments.
In mRNA research used by Pfizer – a candidate study on mRNA with rhesus macaques monkeys using BNT162b2 mRNA and in that study all monkeys developed pneumonia but the researchers considered the risk low because these were young healthy monkeys from 2-4 years of age.
Israel has used Pfizer and the International Court of Justice has accepted a requirement that 80% of recipients with pneumonia should be injected with this gene therapy.
Despite this alarming development, Pfizer continued to develop its mRNA for Covid, without animal testing.
Nuremberg Code # 4: Avoid all unnecessary suffering and injury
Since the launch of the experiment and listed under the CDC VAERS reporting system, over 4,000 deaths and 50,000 vaccine injuries have been reported in the United States. In the EU, more than 7,000 deaths and 365,000 vaccine injuries have been reported. This is a serious violation of this code.
Nuremberg Code # 5: No experiment should be performed if there is reason to believe that injury or death will occur
See No. 4, based on fact-based medical data, this gene therapy causes death and injury. Previous research on mRNA also shows several risks that have been ignored for this current experimental gene experiment. A 2002 study of SARS-CoV-1 nail proteins showed that they cause inflammation, immunopathology, blood clots and inhibit Angiotensin 2 expression. This experiment forces the body to produce this nail protein that inherits all these risks.
Nuremberg Code # 6: The risk should never exceed the benefit
Covid-19 has a recovery rate of 98-99%. Vaccine damage, death, and adverse side effects of mRNA gene therapy far outweigh this risk.
The use of “leaky” vaccines was banned for agricultural use by the US and the EU due to the Marek Chicken study which shows “hot viruses” and variants appear… make the disease even more deadly.
Nevertheless, this has been ignored for human use by the CDC aware that the risk of new, more deadly variants arises from leaky vaccinations. The CDC is fully aware that the use of leaky vaccines facilitates the emergence of hotter (more deadly) strains. Yet they have ignored this when it comes to humans
Nuremberg Code # 7: Preparations must be made for even remote possibilities of injury, disability or death
No preparations were made. This gene therapy skipped animal experiments. The pharmaceutical companies’ own clinical phase 3 studies will not end until 2022/2023. These vaccines were approved in an emergency
Use only action to force on a misinformed public. They are NOT FDA approved.
Nuremberg Code # 8: Experiments must be carried out by scientifically qualified persons
Politicians, the media and actors who claim that this is a safe and effective vaccine are not qualified. Propaganda is not medical science.
Many stores such as Walmart & drive-through vaccine centers are not qualified to administer experimental medical gene therapies to the uninformed public.
Nuremberg Code # 9: Everyone must have the freedom to end the experiment at any time
Despite the call from over 85,000 doctors, nurses, virologists and epidemiologists – the experiment does not end. In fact, there are currently many attempts to change laws to enforce vaccine compliance.
This includes mandatory and mandatory vaccinations. Experimental “sprayers” are planned every six months without using the growing number of deaths and injuries already caused by this experiment.
These update images will be administered without any clinical trials. Hopefully, this new Nuremberg trial will put an end to this crime against humanity.
Nuremberg Code # 10: The researcher must terminate the experiment at any time if there is a probable cause for injury or death
It is clear from statistical reporting data that this experiment leads to death and injury. But not all politicians, pharmaceutical companies and so-called experts make any attempt to stop this gene therapy experiment from harming a misinformed public.
Legal proceedings are progressing, evidence has been gathered and a large growing group of experts is sounding the alarm.