mRNA, or messenger RNA, vaccines are a relatively new player in the vaccine field. Their goal is to invade the body's cells and teach them how they can generate a protein that will spur an immune response to produce antibodies that can prevent infection should an actual virus enter the body.
They are different from traditional vaccines in the sense that they do not use a weakened or live virus in order to cause the desired immune response. Instead, they used genetic material, or mRNA, to provide the instructions for producing the target viral protein. The mRNA is packaged inside a protective lipid nanoparticle that will help the genetic material make its way into the cells. There, it will produce the viral protein so the immune system can recognize it and create antibodies that will neutralize it. This is why many people are likening them to gene therapy injections.
While this may sound like an effective approach in theory, there are actually many shortcomings to the process. However, of greater concern to many people are the potential side effects, many of which are unknown because the technology is so new and there have been no long-term studies on the effects of mRNA COVID-19 vaccines.
We do know, however, that mRNA vaccines can cause a person's immune system to become overstimulated, which is why so many people are experiencing inflammation and autoimmune reactions to the jabs. And while authorities claimed that the mRNA in these vaccines breaks down quickly and is eliminated by the body when they were pushing the jabs on the masses, this has turned out not to be the case at all.
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In fact, these vaccines were given emergency use authorization when clinical trials with them were only in phase 3 and real-world data was already showing a higher mortality rate among vaccinated individuals compared to those who were not vaccinated. They were also showing a higher risk of getting infected with the virus. This and other evidence pointed to COVID-19 vaccines destroying people's natural immune responses.
Another big risk of the jabs was severely underplayed by authorities: the activation of latent viruses. Many scientists were immediately concerned that these jabs could activate dormant viruses such as HIV and herpes and pushed for further research to be conducted into these risks before rolling out the shots.
Latent viruses can sit in the body in a dormant state for extended periods of time without causing any obvious symptoms. However, when the immune system is activated by mRNA jabs and produces chemokines and cytokines that signal molecules to recruit immune cells to the infection site, the cells may recognize and target latent viruses, activating and replicating them.
In addition, we now know that mRNA from these vaccines does not degrade quickly and is not eliminated by the body rapidly. Instead, it multiplies millions of times and can make its way across the blood-brain barrier. This is why these vaccines are perfectly capable of activating latent viruses.
Another big problem with these vaccines is their potential to alter the ability of a person's immune system to recognize and respond to other pathogens. This could compromise the immune system's effectiveness when it comes to fighting off all types of infections and raise a person's risk of disease. This may also help explain why there is a much higher mortality rate among the vaccinated compared to the unvaccinated.
While mRNA vaccines are still the subject of ongoing research, early data shows that the benefits of these jabs do not come close to outweighing the potential risks, particularly when you consider their inability to prevent the transmission of the virus from person to person.
Esteemed Belgian virologist Dr. Geert Vanden Bossche has warned that a huge wave of illnesses and deaths among the highly vaccinated population with their compromised immune systems is just around the corner, causing the collapse of the hospital system and social, financial and economic chaos.
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