The first and foremost point to be made here is that messenger RNA (mRNA) "vaccines" are not legally vaccines at all according to the CDC official definition. The FDA granted “emergency use authorization” for these vaccines (herein “mRNA injections”) because they are unlike conventional vaccines and is required by law to be granted only if there are no effective treatments for COVID-19 (which there are). The moment the "national emergency" that is COVID-19 is called off or an alternate treatment is deemed effective, all of the mRNA injections instantly become unapproved for human use.
Dr. David Martin leads a Zoom discussion between himself Dr. Judy Mikovits, Robert F. Kennedy Jr. and Dr. Rocco Galati in this excerpt from the January 5th, 2021 two-hour online event, “Focus on Fauci”, investigating the man who has been the Globalists’ point man in destroying millions of lives by ushering in the COVID-19-Plandemic-NWO. Dr. David Martin's main point is that if we stipulate this mRNA injection is a vaccine we have already lost the battle.
The reason pharmaceutical companies have conditioned and propagandized society to perceive these experimental injections as vaccines is so they can award themselves the same liability immunity luxuries that are permitted to these companies for vaccines. While simultaneously this forces people to have a discussion about vaccines, when in realty this is a GMO like technology that injects an operating system into the human body designed to alter you by installing synthetic chemical pathogens that overwork the immune system.
Even fake news CNBC agrees that these liability immunities effectively prevent you from being able to sue in a U.S. court of law:
If you experience severe side effects after getting a Covid vaccine, lawyers tell CNBC there is basically no one to blame in a U.S. court of law.
The federal government has granted companies like Pfizer and Moderna immunity from liability if something unintentionally goes wrong with their vaccines.
“It is very rare for a blanket immunity law to be passed,” said Rogge Dunn, a Dallas labor and employment attorney. “Pharmaceutical companies typically aren’t offered much liability protection under the law.”
You also can’t sue the Food and Drug Administration for authorizing a vaccine for emergency use, nor can you hold your employer accountable if they mandate inoculation as a condition of employment.
According to the FDA “An investigational drug can also be called an experimental drug" and all mRNA vaccine candidates identify their new agents as “investigational.” Experimental categorization consists of the following reasons:
the pharmaceutical companies have applied for investigational use status
adverse events will be settled under the legal standard for experimental medications
recipients are enrolled as subjects in a medical trial to gather data on side effects.
persons are enrolled in a pharmaco-vigilance tracking system for at least two years
many groups of persons have not been studied at all, including: prior COVID-19 patients, pregnant women, youths, elderly
no published animal studies data
In the following two images we can see how Moderna and Pfizer both market their mRNA injections as an "operating system" and "software" as the Luciferian Fascist Jesuit Illuminati Freemasonic Cabal must put everything in plain sight to get "manufactured consent" from us to proceed with their eugenics, depopulation, and transhumanist-AI schemes. What we all need to realize is we are born with God given freedoms and rights, which we need to stop allowing globalist organizations and infiltrated governments make our decisions for us.
Moderna chief medical officer Tal Zaks even admits these mRNA injections alter human DNA in a sense of "hacking the software of life", listen to the segment of his TEDx Talk below.
Moderna is happily experimenting on humans with mRNA injections that they openly know alter our DNA and result in adverse effects all for their cabalistic agenda and monetary gain. In fact, Moderna had a 1383% revenue increase thanks to their mRNA injection profits of the 2020 fall quarter based on already signed agreements. Total revenue was $803 million for the year ending December 31, 2020 compared to only $60 million for the year ending December 31, 2019.
Let us take a moment to factor in the murky ethics surrounding health care institutions and workplaces compensating or pressuring employees into taking experimental mRNA injections which violate points 1, 4, 6, and 10 of the Nuremberg Code (1947) as seen below:
A.G. Rhodes Cobb nursing home in Atlanta, Wisconsin is providing a measly $150 bonus for staff who complete both doses of the COVID-19 vaccine.
Houston Methodist Hospital in Texas is offering a $500 “hope bonus” to workers who willingly accept the COVID-19 vaccine.
The Gracedale Nursing Home in Nazareth, Pennsylvania is offering employees who take the injection a one-time payment of $750.
Aldi, American Airlines, Amtrak, Bolthouse Farms, Dollar General, Instacart, Kroger, McDonald's, Publix, Target & Trader Joe's amongst a growing list of companies paying their employees to receive the COVID-19 vaccine with any of the following incentivized variations:
Employee recognition programs
Extra days off
Free transportation to vaccination sites via Lyft
Paid time off
Furthermore, in relation to violating the Nuremberg Code (1947), The Corona Investigative Committee was established by four lawyers in Germany including: Dr. Reiner Fuellmich, Dr. Viviane Fischer, Justus Hoffmann and Antonia Fischer. Since July 10, 2020 they have been working with attorneys worldwide gathering testimonials for an international class-action lawsuit from a large number of international scientists and experts. The main highlighted points from their accumulated conclusions include:
The corona crisis must be renamed the “Corona Scandal” for being the biggest tort case ever and the greatest crime against humanity ever committed
Those responsible must be criminally prosecuted for crimes against humanity and sued for civil damages
Relatedly, lawyers Ruth Makhacholovsky and Aryeh Suchowolski have successfully brought forward a lawsuit to the International Criminal Court (The Hague, Netherlands). This lawsuit has been accepted and acknowledged by Mark Dillion (Head of Information & Evidence Unit) regarding crimes against humanity for the experimental mRNA COVID-19 injection testing pertaining to the multiple violations of the Nuremberg Code by the Israeli government unlawfully pressuring their citizens to get vaccinated or face discrimination.
By March 18, 2021 the Natural & Common Law Tribunal For Public Health & Justice (a.k.a. PeaceInSpace.org) had issued its final order including a judgement enforcement and compliance order regarding ceasing and desisting distribution of all COVID vaccinations as they are considered to be genetic biowarfare thus constituting as geocide and crimes against humanity. Both the judgement enforcement and compliance order documents are linked within this cease and desist order. Please issue this cease and desist order to all complicit corporations, all levels of government, and all administering healthcare providers In your region (effective worldwide).
As of April 19, 2021 the Natural & Common Law Tribunal For Public Health & Justice (a.k.a. PeaceInSpace.org) released a media update that they successfully filled communications with the prosecutor at the International Criminal Court (The Hague, Netherlands) on April 17, 2021.
Researchers from Sloan Kettering Cancer Center published a summary on August 27, 2018 stating that changes to mRNA essentially promote cancer. Up to December 3, 2020 that summary remained unchanged, however come January 13, 2021 the Sloan Kettering Institute found it critical to make an amendment specifying that these "previously unknown drivers of the disease" a.k.a. cancer have nothing to do with mRNA technology based injections developed against SARS-CoV-2 (COVID-19).
Researchers at the Sloan Kettering Institute have found that changes in an information-carrying molecule called messenger RNA can inactivate tumor-suppressing proteins and thereby promote cancer. The findings pinpoint previously unknown drivers of the disease.
This brings our attention to the FDA and their Vaccines and Related Biological Products Advisory Committee October 22, 2020 meeting presentation. In plain sight they list nearly two dozen "adverse event outcomes" from the time of publishing. Imagine if this experimental mRNA injection technology is actually studied properly with clinical trials how many additional negative adverse side effects will be uncovered with regards to mid and long term complications. Clinical trials are not set to finish until 2023, meaning all the indoctrinated sheep willingly and eagerly getting experimental mRNA injections are a live walking contagious experiment.
Speaking of sheep and trials relating to mRNA COVID-19 injections, Colleen Huber, NMD, released a report titled "COVID-19 Vaccine Considerations" on February 21, 2021 that highlighted:
This technology has been tried on animals, and in the animal studies done, all the animals died, not immediately from the injection, but months later, from other immune disorders, sepsis and/or cardiac failure. There has never been a long-term successful animal study using this technology. No experimental coronavirus vaccine has succeeded in animal studies.
Moreover, we have an evidence review from the Penn Medicine Center for evidence-based practice which openly concludes "the rate of severe adverse effects (severe enough to interfere with a person’s daily activities) appears to be in the range of 5 to 10 percent. The rate and severity of adverse events increases with vaccine dose. The rate and severity of adverse events also appears to be greater following a second dose of vaccine than following the first."
Does anything sound wrong to you about pushing mRNA injections where 5-10% of clinical trials result in adverse effects? Where rate and severity of adverse events increases with further dosages... All for the alleged "disease" coronavirus (common cold) with a 99.9% survival rate for people 69 and under.
These adverse effects have already been heavily reported across the world, commonly as severe allergic reactions such as in Dr. Hossein Sadrzadeh case back in December 2020. Increasingly, reports are also surfacing worldwide of people dying after their second dosage of the mRNA injection, almost as if it is the kill switch to go along with the first dosage. The following are examples of people falling ill or dying after receiving either the first or second dosage of either the Moderna or Pfizer mRNA COVID-19 operating system injection:
As of April 28, 2021 Pfizer had openly admitted that their experimental mRNA BioNTech injections were guilty of viral shedding, conveniently coined "occupational exposure" in their clinical study. Therefore this technology is immorally vaccinating the unknowing unvaccinated populations that make unplanned contact with the mRNA injected/vaccinated. This is a blatant violation of the Nuremberg Code (1947) and is further evidence that experimental mRNA injections for COVID are in fact genetic biowarfare. This comes straight out of the Pfizer BioNTech study (PF-07302048) titled "A Phase 1/2/3 Study to Evaluate the Safety, Tolerability, Immunogenicity, and Efficacy of RNA Vaccine Candidates Against COVID-19 in Healthy Individuals" where the direct quote can be seen below.
188.8.131.52. Occupational Exposure An occupational exposure occurs when a person receives unplanned direct contact with the study intervention, which may or may not lead to the occurrence of an AE. Such persons may include healthcare providers, family members, and other roles that are involved in the trial participant’s care. The investigator must report occupational exposure to Pfizer Safety within 24 hours of the investigator’s awareness, regardless of whether there is an associated SAE. The information must be reported using the Vaccine SAE Report Form. Since the information does not pertain to a participant enrolled in the study, the information is not recorded on a CRF; however, a copy of the completed Vaccine SAE Report Form is maintained in the investigator site file.
To clarify the quotation from the study in laymen's terms, an occupational exposure (viral shedding) occurs when an individual comes in contact with an injected mRNA trial test subject (a super spreader) which likely results in the occurrence of adverse effects for unvaccinated individuals. These adverse effects caused by viral shedding are strictly being reported on VAERS and not within any clinical mRNA studies as the information does not pertain to a participant enrolled in the study. In conclusion, we now have direct official confirmation from Pfizer to stay away from the "vaxxed" mRNA injected individuals as they are the true super spreaders and conspiracists worldwide are once again vindicated.
These adverse effects and sudden deaths after dosages are no surprise as Dr. Sherri Tenpenny (known as the most knowledgeable and outspoken physician on the adverse impact that vaccines can have on health) already warned the world that the COVID vaccines’ depopulation effects will start in 3 to 6 months from point of injection. Reinette Senum interviews Dr. Tenpenny in the following video where she describes the "religion of vaccination indoctrination" as vaccines now and always have been "a method of mass destruction, a method of depopulation, and a method of creating customers for life."
Equivalently, Dr. Lee Merritt of America’s Frontline Doctors shares a similar opinion to Dr. Tenpenny in her interview with The Sons of Liberty where she explains experimental operating system Injections are going to result in a lot of deaths. Take a look at the following interview.
On another note, an angelic anonymous naturopathic doctor under the alias Herbal Sage Queen has conducted a commentary review on Baden, L.R. et al.'s "Efficacy and Safety of the mRNA-1273 SARS-CoV-2 Vaccine" Baden, L.R. et al.'s "Efficacy and Safety of the mRNA-1273 SARS-CoV-2 Vaccine" (Dec 2020 - NEJM DOI: 10.1056/NEJMoa2035389) as follows:
The trial enrolled 30,420 volunteers who were randomly assigned in a 1:1 ratio to receive either vaccine or placebo (15,210 participants in each group).
The primary end point was prevention of Covid-19 illness [not infection] with onset at least 14 days after the second injection in participants who had not previously been infected with SARS-CoV-2.
The mRNA-1273 vaccine showed 94.1% efficacy at preventing Covid-19 illness [NOT infection], including severe disease.
Covid-19 cases were defined as occurring in participants who had at least two of the following symptoms: fever (temperature ≥38°C), chills, myalgia, headache, sore throat, or new olfactory or taste disorder, or as occurring in those who had at least one respiratory sign or symptom (including cough, shortness of breath, or clinical or radiographic evidence of pneumonia) and at least one nasopharyngeal swab, nasal swab, or saliva sample (or respiratory sample, if the participant was hospitalized) that was positive for SARS-CoV-2 by reverse-transcriptase–polymerase-chain-reaction (RT-PCR) test.
This definition of COVID-19 excludes asymptomatic cases, including those who tested positive for COVID-19, which is a large amount of positive cases. This study design also excludes the question for whether or not the vaccine has any preventative properties.
Participants were assessed for the presence of SARS-CoV-2–binding antibodies specific to the SARS-CoV-2 nucleocapsid protein (Roche Elecsys, Roche Diagnostics International) and had a nasopharyngeal swab for SARS-CoV-2RT-PCR testing (Viracor, Eurofins Clinical Diagnostics) before each injection.
Common reasons for not receiving the second dose were withdrawal of consent (153 participants) and the detection of SARS-CoV-2 by PCR before the administration of the second dose on day 29 (114 participants: 69 in the placebo group and 45 in the mRNA- 1273 group).