Humans Are Free: Experimental Gene Therapies
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Did you know that mRNA COVID-19 vaccines aren’t vaccines in the medical and legal definition of a vaccine?
They do not prevent you from getting the infection, nor do they prevent its spread. They’re really experimental gene therapies.
I discussed this troubling fact in a recent interview with molecular biologist Judy Mikovits, Ph.D. While the Moderna and Pfizer mRNA shots are labeled as “vaccines,” and news agencies and health policy leaders call them that, the actual patents for Pfizer’s and Moderna’s injections more truthfully describe them as “gene therapy,” not vaccines.
Definition Of ‘Vaccine’
According to the U.S. Centers for Disease Control and Prevention,1 a vaccine is “a product that stimulates a person’s immune system to produce immunity to a specific disease, protecting the person from that disease.”
Immunity, in turn, is defined as “Protection from an infectious disease,” meaning that “If you are immune to a disease, you can be exposed to it without becoming infected.”
Neither Moderna nor Pfizer claim this to be the case for their COVID-19 “vaccines.” In fact, in their clinical trials, they specify that they will not even test for immunity.
Unlike real vaccines, which use an antigen of the disease you’re trying to prevent, the COVID-19 injections contain synthetic RNA fragments encapsulated in a nanolipid carrier compound, the sole purpose of which is to lessen clinical symptoms associated with the S-1 spike protein, not the actual virus.
They do not actually impart immunity or inhibit transmissibility of the disease.
In other words, they are not designed to keep you from getting sick with SARS-CoV-2; they only are supposed to lessen your infection symptoms if or when you do get infected.
As such, these products do not meet the legal or medical definition of a vaccine, and as noted by David Martin, Ph.D., in the video above, “The legal ramifications of this deception are immense.”
15 U.S. Code Section 41
As explained by Martin, 15 U.S. Code Section 41 of the Federal Trade Commission Act2 is the law that governs advertising of medical practices.
This law, which dictates what you may and may not do in terms of promotion, has for many years been routinely used to shut down alternative health practitioners and companies.
“If this law can be used to shut down people of good will, who are trying to help others,” Martin says, “it certainly should be equally applied when we know deceptive medical practices are being done in the name of public health.”
Per this law, it is unlawful to advertise:
“… that a product or service can prevent, treat, or cure human disease unless you possess competent and reliable scientific evidence, including, when appropriate, well-controlled human clinical studies, substantiating that the claims are true at the time they are made.”3
COVID-19 Vaccines — A Case Of False Advertising
Now, if the COVID-19 vaccine really isn’t a vaccine, why are they calling it that? While the CDC provides a definition of “vaccine,” the CDC is not the actual law. It’s an agency empowered by the law, but it does not create law itself.
Interestingly enough, it’s more difficult to find a legal definition of “vaccine,” but there have been a few cases. Martin provides the following examples:
• Iowa code — “Vaccine means a specially prepared antigen administered to a person for the purpose of providing immunity.” Again, the COVID-19 vaccines make no claim of providing immunity. They are only designed to lessen symptoms if and when you get infected.
• Washington state code — “Vaccine means a preparation of a killed or attenuated living microorganism, or fraction thereof …” Since Moderna and Pfizer are using synthetic RNA, they clearly do not meet this definition.
Being a manmade synthetic, the RNA used is not derived from anything that has at one point been alive, be it a whole microorganism or a fraction thereof. The statute continues to specify that a vaccine “upon immunization stimulates immunity that protects us against disease …”
So, in summary, “vaccine” and “immunity” are well-defined terms that do not match the end points specified in COVID-19 vaccine trials. The primary end point in these trials is: “Prevention of symptomatic COVID-19 disease.” Is that the same as “immunity”? No, it is not.
There Are More Problems Than One
But there’s another problem. Martin points out that “COVID-19 disease” has been defined as a series of clinical symptoms.
Moreover, there’s no causal link between SARS-CoV-2, the virus, and the set of symptoms known as COVID-19.
How is that, you might ask? It’s simple, really. Since a vast majority of people who test positive for SARS-CoV-2 have no symptoms at all, they’ve not been able to establish a causal link between the virus and the clinical disease.
Here’s yet another problem: The primary end point in the COVID-19 vaccine trials is not an actual vaccine trial end point because, again, vaccine trial end points have to do with immunity and transmission reduction. Neither of those were measured.
What’s more, key secondary end points in Moderna’s trial include “Prevention of severe COVID-19 disease, and prevention of infection by SARS-CoV-2.”
However, by its own admission, Moderna did not actually measure infection, stating that it was too “impractical” to do so.
That means there’s no evidence of this gene therapy having an impact on infection, for better or worse. And, if you have no evidence, you cannot fulfill the U.S. Code requirement that states you must have “competent and reliable scientific evidence … substantiating that the claims are true.”
Why Are They Calling Them Vaccines?
As noted by Martin, you cannot have a vaccine that does not meet a single definition of a vaccine.
So, again, what would motivate these companies, U.S. health agencies and public health officials like Dr. Anthony Fauci to lie and claim that these gene therapies are in fact vaccines when, clearly, they are not?
If they actually called it what it is, namely “gene therapy chemotherapy,” most people would — wisely — refuse to take it.
Perhaps that’s one reason for their false categorization as vaccines. But there may be other reasons as well.
Here, Martin strays into conjecture, as we have no proof of their intentions. He speculates that the reason they’re calling this experimental gene therapy technology a “vaccine” is because by doing so, they can circumvent liability for damages.
“You’re being lied to. Your own government is violating its own laws. They have shut down practitioners around the country, time and time again, for violating what are called ‘deceptive practices in medical claims.’ Guess what? They’re doing exactly that thing.” ~ David Martin, Ph.D.
As long as the U.S. is under a state of emergency, things like PCR tests and COVID-19 “vaccines” are allowed under emergency use authorization. And as long as the emergency use authorization is in effect, the makers of these experimental gene therapies are not financially liable for any harm that comes from their use.
That is, provided they’re “vaccines.” If these injections are NOT vaccines, then the liability shield falls away, because there is no liability shield for a medical emergency countermeasure that is gene therapy.
So, by maintaining the illusion that COVID-19 is a state of emergency, when in reality it is not, government leaders are providing cover for these gene therapy companies so that they can get immunity from liability.
Under The Cover Of ‘Emergency’
As noted by Martin, if state governors were to lift the state of emergency, all of a sudden the use of RT PCR testing would be in violation of 15 U.S. Code FTC Act, as PCR tests are not an approved diagnostic test.
“You cannot diagnose a thing [with something] that cannot diagnose a thing,” Martin says. “That a misrepresentation. That is a deceptive practice under the Federal Trade Commission Act. And they’re liable for deceptive practices.”
Importantly, there’s no waiver of liability under deceptive practices — even under a state of emergency. This would also apply to experimental gene therapies. The only way for these gene therapies to enjoy liability shielding is if they are vaccines developed in response to a public health emergency. There is no such thing as immunity from liability for gene therapies.
Propaganda And Vaccine Rollout Run By Same Company
Martin brings up yet another curious point. The middleman in Operation Warp Speed is a North Carolina defense contractor called ATI. It controls the rollout of the vaccine. But ATI also has another type of contract with the Department of Defense, namely managing propaganda and combating misinformation.
So, the same company in charge of manipulating the media to propagate government propaganda and censor counterviews is the same company in charge of the rollout of “vaccines” that are being unlawfully promoted.
“Listen,” Martin says. “This is a pretty straight-forward situation. You’re being lied to. Your own government is violating its own laws … They have thrown this book [15 U.S. Code Section 41] on more people than we can count.
“They have shut down practitioners around the country, time and time again, for violating what are called ‘deceptive practices in medical claims’ … Guess what? They’re doing exactly that thing.”
Martin urges listeners to forward his video to your state attorney, governor, representatives and anyone else that might be in a position to take affirmative action to address and correct this fraud.
Defense contractors are violating FTC law, and gene therapy companies — not vaccine manufacturers — are conducting experimental trials under deceptive medical practices.
They’re making claims of being “vaccines” without clinical proof, and must be held accountable for their deceptive marketing and medical practices.
CDC Owns Coronavirus Patents
On a side note, the CDC appears to be neck-deep in this scam pandemic, and is therefore wholly unsuitable to investigate the side effects of these experimental COVID-19 therapies. As noted by Martin, it’s like having a bank robber investigate its own crime.
Details about this came out in the documentary “Plandemic,” in which Martin explained how the CDC has broken the law — in one way or another — related to its patenting of the 2003 SARS virus.
Martin is a national intelligence analyst and founder of IQ100 Index, which developed linguistic genomics, a platform capable of determining the intent of communications.
In 1999, IBM digitized 1 million U.S. patents, which allowed Martin’s company to conduct a review of all these patents, sending him down a proverbial “rabbit trail” of corruption.
In 2003, Asia experienced an outbreak of SARS. Almost immediately, scientists began racing to patent the virus.
Ultimately, the CDC nabbed ownership of SARS-CoV (the virus responsible for SARS) isolated from humans.
So, the CDC actually owns the entire genetic content of that SARS virus. It’s patented under U.S. patent 7776521. They also own patents for detection methods, and for a kit to measure the virus.
U.S. patent 7279327,5 filed by the University of North Carolina at Chapel Hill, describes methods for producing recombinant coronaviruses.
Ralph Baric, Ph.D., a professor of microbiology and immunology who is famous for his chimeric coronavirus research, is listed as one of the three inventors, along with Kristopher Curtis and Boyd Yount.
According to Martin, Fauci, Baric and the CDC “are at the hub” of the whole COVID-19 story.
“In 2002, coronaviruses were recognized as an exploitable mechanism for both good and ill,” Martin says, and “Between 2003 and 2017, they [Fauci, Baric and CDC] controlled 100% of the cash flow to build the empire around the industrial complex of coronavirus.”
How The CDC Broke The Law
The key take-home message Martin delivers in “Plandemic” is that there’s a distinct problem with the CDC’s patent on SARS-CoV isolated from humans, because, by law, naturally occurring DNA segments are prohibited from being patented.