Have you been told that we can’t take civil or criminal action against Big Pharma or the government? Do you want to know why no criminal charges have been brought against Pfizer, Moderna, J&J, the FDA, HHS, CDC, NIH, and others involved in the development, manufacturing, distribution, promotion, and administration of these bioweapons falsely referred to as mRNA vaccines? It could be because 99.9% of Americans are victims ofextrinsic fraud, or in non-legal terms, narcissistic gaslighting.
Gaslighting is the intentional use of repetitive and patterned manipulation techniques to make individuals, groups, or even entire populations question their reality. Gaslighting is often used by influential people with narcissistic personality disorder (NPD) as means of gaining power, by making people dependent on them for information and guidance. Once authority and trust are established, NPD individuals can easily mislead others about material facts and their legal rights in matters of civil or criminal litigation. They often will discredit anyone who questions their statements, authority, or intentions in order to maintain control of a narrative or group of people.
Be wary of attorneys or leaders who tell you that organizations that have harmed, disabled and murdered hundreds of thousands of American adults and innocent children; organizations such as Pfizer, that the lawsdon’t apply to them.
When an expert or attorney withholds material evidence or misrepresents the facts and laws regarding a legal matter, such as a potential lawsuit, it’s called extrinsic fraud.
Extrinsic fraud is fraud that induces a person; to not present a case in court, to not pursue criminal charges, to not properly present case, or to be deprived of an opportunity for just compensation.
- Extrinsic fraud includes fraudulent acts which keep a person from understanding information about his/her rights or obtaining evidence. This could include misleading an ignorant person about not having the right to sue or press criminal charges, or persuading them to delay moving forward with a case (stalling tactics).
- A typical stall tactic used by attorneys and politicians is telling victims and frustrated constituents to ‘just wait’, ‘the team is working on it’, and that they will ‘hold an investigation to hold these criminals to account.’ – These are stalling tactics.
- Extrinsic fraud is distinguished from intrinsic fraud, which is the fraud that is the subject of a lawsuit (i.e. Pfizer and the FDA committed intrinsic fraud regarding the clinical trial data.).
It is not uncommon for a judge, attorney or politician to commit the crime of extrinsic fraud due to bribery, coercion, or allegiance to an undisclosed organization or individual. Experts who have special knowledge of material facts also engage in extrinsic fraud for the same reasons listed above.
Typically, extrinsic fraud occurs once legal matters officially begin, such as engaging an attorney, but it’s safe to say that many Americans have been gaslit into believing there is nothing we can do to pursue Big Pharma or the government healthcare agencies.
Below are some false claims that have been repeated to us consistently and relentlessly.
- Pfizer is protected under EUA immunity.
- The FDA/VRBPAC can change the definition of a vaccine to whatever they want.
- Pfizer is protected under the Childhood Vaccine Injury Act because the CDC added it to the Childhood Vaccine Schedule.
In my opinion, these false and misleading statements have dissuaded Americans from pursuing criminal or civil charges against Big Pharma (Pfizer) and/or the government agencies they conspired with for manufacturing, distributing, promoting and administering mRNA bioweapons on American adults, seniors, and our children.
Not only are these repeated claims false, but they are also irrelevant. Why? Because the COVID-19 mRNA injections are not vaccines.The COVID-19 mRNA injections are biological weapons.
Per18 USC 175, a biological weapon is any biological agent, toxin, or delivery system (device/LNP/vaccine) that is not reasonably justified by a prophylactic or protective purpose; bona fide research,or other peaceful purposes.
It’s critical that we’re able to clearly articulate and document that the COVID-19 mRNA vaccines are weapons of biowarfare and stop repeating the lie that the COVID-19 mRNA injections are vaccines that underwentbona fide research and are able to provide prevention from infection or protection from disease.
Let’s apply some techniques from the Socratic method to define what the mRNA injections ‘are not’ through statements and claims from FDA an Pfizer documents, and then apply those statements and claims to define what the mRNA injections are.
When I point out to attorneys and scientific experts that the COVID-19 mRNA injections aregene-editing technologies that do not provide immunity and actually cause disease, the typical response has been something along the lines of, “FDA/CBER/VRBPAC can call a a gene-editing technology a vaccine, a medical device a vaccine, or anything they want a vaccine.”
This is a false, manipulative, misleading and fraudulent statement.
But for the sake of argument, let’s say the attorneys are right (and not just lying), and that the FDA has the authority to change the name of therapeutic categories on a whim (or at Pfizer’s command). Let’s say the FDA has the legal authority to call PEGylated lipid nanoparticle encapsulated gene-editing technologies that produce immunogenic disease causing and sometimes life-threatening biosynthetic spike proteins whatever the agency wants; baby aspirin, an antibiotic, or a vaccine.
Even if this was true (that the FDA could call a gene-editing technology a vaccine), this still means that the Phase-3 data and post-market approval data for Pfizer’s COVID-19 mRNA vaccines must meet the burden-of-proof of proving vaccine efficacy per the FDA-approvedindicationfor their ‘vaccine.’
The indication for Pfizer’s FDA-approved COVID-19 mRNA vaccines is;
“…TO PREVENT coronavirus DISEASE – 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2).”
Now let’s apply the FDA’s and Pfizer’s own evidence against them. (Much of this content is taken fromIntended Consequences).
During the FDA’sDecember 11, 2020, emergency use authorization meeting for the Pfizer COVID-19 mRNA vaccines, FDA committee members pointed out that the mRNA vaccines appear to provide no clinical benefit, specifically regarding severe disease.
“ FDA pointed out that vaccine development has a long history and that FDA is not aware of an example of any vaccine that is effective against mild disease that is not also effective against severe disease ” – FDA EUA Review Committee, Pfizer EUA COVID-19 mRNA vaccines, Dec 11, 2020
Per the FDA’s own words, in the history of the FDA, the FDA has never approved a vaccine that does not protect against severe disease, until the agency approved the COVID-19 mRNA vaccines.
Per the data discussed during that same FDA meeting, not only doPfizer’s COVID-19 mRNA vaccines NOT prevent severe disease, Pfizer’s mRNA vaccines cause SEVERE COVID-19 within 7 days of being injected.
Page 41 of PFIZER’s EUA submission, states that there were 409 patients who had COVID-19 symptoms within 7 days of getting their first (1st) or second (2nd) PFIZER shot, BUT these patients did not have a positive PCR-test for SARS-CoV-2.
Per PFIZER’s own document, “unconfirmed COVID-19 cases could have masked clinically significant adverse events that would have otherwise been detected.”
Per PFIZER’s EUA submission, clinically significant or severe COVID-19 cases were defined in the Phase-3 Study as kidney, liver or neurological dysfunction, low oxygen levels, respiratory failure, mechanical ventilation, systemic shock, admission to the intensive care unit (ICU), or death.
Per the September 17, 2021,FDA committee meeting, the FDA had full knowledge that two (2) injections of Pfizer’s mRNA vaccines increases a person risk for developing COVID-19 over time versus a person who remains unvaccinated.
Per the documents provided to the FDA for the authorization and approval of Pfizer’s COVID-19 mRNA vaccines, the mRNA vaccinescauseSARS-CoV-2 infection and COVID-19 disease, including severe disease.
Pfizer’s COVID-19 mRNA vaccines increase the risk of COVID-19 caused by SARS-CoV-2, therefore they cannot prevent SARS-CoV-2 infection or prevent COVID-19 (per the FDA-approved indication) and do not meetthe FDA’s definition of a vaccine.
A biological weapon is any biological agent or delivery system (LNPs and vaccines) that is not reasonably justified by a prophylactic or protective purpose; or bona fide research.
mRNA Injection Evidence:Vaccine- 0 Bioweapon-5
The COVID-19 mRNA injections produce patented, synthetically recreated 2-proline mutation spike proteins that;
- do NOT produce antibodies to SARS-CoV-2, and
- are resistant to the antibodies for SARS-CoV-2, and therefore –
It is scientifically and clinically impossible for Pfizer’s authorized and FDA-approved mRNA vaccines to be considered a vaccine, or a prophylactic or preventative treatment against SARS-CoV-2 infection, or any coronavirus, including variants.
mRNA Injection Evidence:Vaccine- 0 Bioweapon-6
Let’s say an attorney or Albert Bourla himself claims that, “Fine, the mRNA injections may not be these so-called ‘vaccines’ you speak of, but they are very good emergency use authorized (EUA) gene-editing therapies and anyone who calls them a bioweapon is obviously crazy…..”
Even though in Pfizer’s FDA- approved biological license application (BLA), they describe their mRNA injections as a gene-therapy, they arenot gene-therapies. Gene-therapies prevent or cure disease, and the mRNA injections cause disease.
The following statement from theManufacturingsection of Pfizer’s FDA approval application describes the mechanism-of-action (MOA) of Pfizer’s mRNA as gene therapy:
(The mRNA) are designed for mediating high RNA stability andtranslation efficiency. During RNA transcription, (blank) is replaced with the (blank). This nucleoside substitution has been demonstrated to enhance translation of in vitro transcribed mRNAwhile reducing its reactogenicity.
The mechanism-of-action listed inCOMIRNATY’s FDA application is nearly verbatim to the FDA’s definition for all gene-therapy products per the FDA’s August 2015 Guidance for Industry document, “Design and Analysis of Shedding Studies for Virus or Bacteria-Based Gene Therapy and Oncolytic Products.”
Per the FDA document, “Gene therapy products ARE ALL PRODUCTS that mediate their effects by transcription and/or translation of transferred genetic material (mRNA) and/or by integrating into the host genome and that are administered as nucleic acids, viruses, or genetically engineered microorganisms.
mRNA products may be used to modify cells in vivo (inside the body).”
The mechanism-of-action for Pfizer’s mRNA gene-editing technologies states that during RNA transcription,substitutionoccurs.
Substitution is a type of genetic mutation that has profound effects on human health.
Source: 13 Reasons to Have State Attorney Generals Seize and Destroy All COVID-19 mRNA Bioweapons