December 9, 2021, their paper was reprinted in the Townsend Letter, the Examiner of Alternative Medicine. Seneff, Ph.D., a senior research scientist at MIT who has been conducting research at MIT for over five decades, has spent a large portion of her career investigating the hazards and mechanisms of action of glyphosate.
- The first-ever use of PEG in an injection
- The first-ever use of mRNA gene transfer technology against an infectious agent
- The first-ever “vaccine” to make no clear claims about reducing infection, transmissibility or death
- The first-ever coronavirus vaccine ever tested on humans (and previous coronavirus vaccines all failed due to antibody-dependent enhancement, a condition in which the antibodies actually facilitate infection rather than defend against it)
- The first-ever use of genetically modified polynucleotides in the general population
An Insanely Reckless ProcessIn a May 2021 interview with me, Seneff said:
“To have developed this incredibly new technology so quickly, and to skip so many steps in the process of evaluating [its safety], it's an insanely reckless thing that they've done. My instinct was that this is bad, and I needed to know [the truth].
mRNA Jabs Are Shockingly HazardousAs of December 3, 2021, the U.S. Vaccine Adverse Event Reporting System (VAERS) has logged an astounding 927,738 COVID jab related adverse events, including 19,886 deaths. VAERS can receive reports from vaccine manufacturers and other international sources, and if we exclude those, the death toll reported in U.S. territories exclusively stands at 9,136.
Of the total death reports, Pfizer — the only company that the U.S. Food and Drug Administration has granted full licensing for an as-yet unavailable COVID shot — accounts for the vast majority: 13,268, compared to 4,894 for Moderna, 1,651 for Janssen and 73 for an undisclosed brand.
- Heart problems such as heart attacks and myopericarditis
- Thrombocytopenia (low platelet count)
- Bell’s palsy
- A variety of permanent disabilities, many of which involve neurological dysfunction
The Cure Is Indeed Worse Than the DiseaseCalculations performed by Steve Kirsch, executive director of the COVID-19 Early Treatment Fund, and his team of statisticians suggest VAERS COVID-related reports are underreported by a factor of 41. This is a conservative estimate, supported by calculations using a variety of sources besides VAERS itself.
That means that in the U.S. alone (using the data for U.S. territories only), the actual death toll may be closer to 374,576 (including international deaths reported to VAERS would put the death toll at 815,326), and those are deaths that occurred within days or weeks post-injection.
As Seneff and Nigh explain in their paper, there’s overwhelming reason to suspect that these gene transfer injections will have devastating impacts in the long term, resulting in excess deaths over the next decade.
What’s more, it’s clear that the death toll from the COVID-19 infection itself in the U.S. has been vastly exaggerated, as it’s based on positive PCR tests and even mere suspicion of COVID in the absence of testing. Many died from other causes and just happened to have a positive COVID test at the time of death.
As predicted in the title of Seneff’s paper, it seems the cure may indeed end up being worse than the disease. This is particularly true for children and young adults, who have either died or been permanently disabled by the shots by the thousands, while having an extraordinarily low risk of dying from or being seriously harmed by the infection itself.
“Seneff suspects that in the next 10 to 15 years, we’ll see a dramatic spike in prion diseases, autoimmune diseases, neurodegenerative diseases at younger ages, and blood disorders such as blood clots, hemorrhaging, stroke and heart failure.”
The Spike Protein Is the Most Dangerous Part of SARS-CoV-2The reason we’re seeing all these problems from the COVID shots is because they program your cells to continuously produce SARS-CoV-2 spike protein, which we now know is the most dangerous part of the virus. Many experts noted this from the start, wondering what the vaccine developers could possibly be thinking, selecting this as the antigen for their shots.
While the mRNA injections can cause harm in many different ways, one basic problem is that they can overstimulate your immune system to the point of failure. In summary, as your cells start producing the viral spike proteins, your immune cells rally to mop up the proteins and dump them into your lymphatic system. (This is why many report swollen lymph nodes under the arms.)
The antibody response is part of your humoral immunity. You also have cellular immunity, which is part of your innate immune system. Your innate immune system is very powerful. If you're healthy, it can clear viruses without ever producing a single antibody. Antibodies are actually a second-tier effect when your innate immune system fails.
The problem is that your innate immune system will not be activated and likely will fail to protect you if you get a COVID-19 shot, because it’s bypassing all of the areas where your innate immune system would be brought to bear.
Normally you breathe the virus in and stimulate the production secretory IgA antibodies that protect your respiratory system. When you bypass that route of exposure with a jab in the arm, no secretory IgA antibodies are produced, leaving you susceptible to the infection.
“An effective vaccine would focus on cellular immunity in the respiratory and intestinal tract, in which secretory IgA is produced by your lymphocytes that are located directly underneath the mucous membranes that line the respiratory and intestinal tract.
“A natural infection with SARS-CoV-2 (coronavirus) will in most individuals remain localized to the respiratory tract,” Kostoff writes. “The vaccines used presently cause cells deep inside our body to express the viral spike protein, which they were never meant to do by nature.
Effects Likely to Persist Long TermWhat’s more, the synthetic RNA in the mRNA vaccines contains a nucleotide called methyl-pseudouridine, which your body cannot break down, and the RNA is programmed to trigger maximum protein production. So, we’re looking at completely untested manipulation of RNA.
It is very important to recognize that this is a genetically engineered mRNA for the spike protein. It is not identical to the spike protein mRNA that SARS-Cov-2 produces. It’s been significantly altered to avoid being metabolized by your body.
The spike protein your body produces in response to the COVID-19 vaccine mRNA locks into your ACE2 receptor. This is because the genetically engineered new spike protein has additional prolines inserted that prevent the receptors from properly closing, which then cause you to downregulate ACE2. That’s partially how you end up with problems such as pulmonary hypertension, ventricular heart failure and stroke.
As noted in a 2020 paper, there’s a “pivotal link” between ACE2 deficiency and SARS-CoV-2 infection. People with ACE2 deficiency tend to be more prone to severe COVID-19. The spike protein suppresses ACE2, making the deficiency even worse. According to Seneff, the gene transfer injections essentially do the same thing, and we still don’t know how long the effects last.
Manufacturers initially guessed the synthetic RNA might survive in the human body for about six months. A more recent investigation found the spike protein persisted in recovered COVID patients for 15 months.
This raises the suspicion that the synthetic and more persistent mRNA in the COVID shots may trigger spike protein production for at least as long, and probably longer. What’s more, the number of spike proteins produced by the shots is far greater than what you experience in natural infection.
As explained by Dr. Peter McCullough, this means that after your first shot, your body will produce spike protein for at least 15 months. But, when you get shot No. 2 a few weeks later, that shot will cause spike protein production to go on for 15 months or longer. With shot No. 3 six months after that, you produce spike protein for yet another 15 months.
Long-Term Neurological Damage Is To Be ExpectedIn her paper, Seneff describes several key characteristics of the SARS-CoV-2 spike protein that suggests it acts as a prion. This could help explain why we’re seeing so many neurological side effects from the shots. According to Seneff, the spike protein produced by the COVID shot, due to the modifications made, may actually make it more of a prion than the spike protein in the actual virus, and a more effective one.
Lung, Heart and Brain Diseases Are Predictable ConsequencesSeneff also goes into great detail describing how the spike protein acts as a metabolic poison. While I recommend reading Seneff’s paper in its entirety, I’ve extracted some key sections below, starting with how the spike protein can trigger pathological damage leading to lung damage and heart and brain diseases:
“The picture is now emerging that SARS-CoV-2 has serious effects on the vasculature in multiple organs, including the brain vasculature … In a series of papers, Yuichiro Suzuki in collaboration with other authors presented a strong argument that the spike protein by itself can cause a signaling response in the vasculature with potentially widespread consequences.
The COVID Shots Activate Latent VirusesAs mentioned earlier, shingles infection is turning out to be a rather common side effect of the COVID shot, and like the neurological, vascular and cardiac damage we’re seeing, activation of latent viral infections was also predicted.
One reason why latent viral infections are cropping up in response to the shots is because the shots disable your type I interferon pathway. A second reason is because your immune system is overburdened trying to deal with the inflammatory spike proteins flowing through your body. Something’s got to give, so latent viruses are allowed to break through.
That’s not the end of your potential troubles, however, as these coinfections may worsen or accelerate other conditions, such as Bell’s Palsy, myalgic encephalomyelitis and chronic fatigue syndrome.
Herpes viruses, for example, have been implicated as a trigger of both AIDS and chronic fatigue syndrome. Some research suggests these diseases don’t appear until viruses from different families partner up and the type 1 interferon pathway is disabled.