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This means that in the United States alone (using data for U.S. territories only), the actual death toll could be closer to 374,576 (including international deaths reported to VAERS would bring the death toll to 815,326), and these have died within a few days or weeks after the injection.

As Seneff and Nigh explain in their article, there is overwhelming reason to suspect that these gene transfer injections will have devastating long-term impacts, resulting in excess deaths over the next decade.

Seneff suspects that over the next 10-15 years we will see a dramatic spike in prion diseases, autoimmune diseases, neurodegenerative diseases at a young age, and blood diseases such as blood clots, bleeding, strokes and heart failure.

As predicted in the title of Seneff’s article, it appears that the cure may indeed end up being worse than the disease. This is especially true for children and young adults.

The reason we’re seeing all these problems from COVID sera is because they program your cells to continuously produce the SARS-CoV-2 spike protein. Many experts have noticed this from the start, wondering what the vaccine developers might think, selecting it as the antigen for their sera.

While mRNA injections can cause damage in many different ways, an underlying problem is that they can over-stimulate the immune system to the point of failure. In summary, when your cells start making these proteins, your immune cells gather to absorb them and dump them into the lymphatic system. (This is why many report swollen lymph nodes under their 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 are healthy, it can kill viruses without ever producing a single antibody. Antibodies are actually a second level effect when your innate immune system fails.

The problem is that your innate immune system won’t be activated and probably won’t be able to protect you if you get a COVID-19 vaccine, because it’s bypassing all areas where your innate immune system would be put into play.

Viruses are normally breathed in and the production of secretory IgA antibodies is stimulated, which protect the respiratory system. When bypassing that route of exposure with a puncture in the arm, no secretory IgA antibodies are produced, leaving you susceptible to infection.

When you are injected with the COVID vaccine, your body will induce only circulating IgG and IgA, not secretory IgA, and these types of antibodies do not effectively protect mucous membranes from infection. Thus, the groundbreaking infections we are seeing “confirm the fundamental design flaws” of this gene transfer technology.

“A natural coronavirus infection in most individuals will remain localized in the respiratory tract,” writes Kostoff. 8 “The vaccines currently used cause the deep cells in our body to express the viral spike protein, which they should never have done by nature.

Any cell that expresses this foreign antigen on its surface will be attacked by the immune system, which will involve both IgG antibodies and cytotoxic T lymphocytes. This can occur in any organ, but the damage will be more severe in vital organs.

We are now seeing that the heart is affected in many young people, leading to myocarditis or even sudden cardiac arrest and death. In other words, we are dropping the wrong bomb on the wrong target at the wrong time! “

Eventually, your body will essentially believe that your innate immune system has failed, which means it has to carry the spare cavalry. Basically, your body is now overreacting to something that isn’t true. You haven’t actually been infected with a virus and your innate immune system hasn’t failed, but your body is forced to respond as if both were real.

Effects likely to persist over the long term

Additionally, the synthetic RNA in 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 RNA manipulation.

It is very important to recognize that this is a genetically modified mRNA for the spike protein. It is not identical to the mRNA of the hypothesized spike protein that would produce SARS-Cov-2. It was basically created to avoid being metabolized by your body.

The spike protein your body produces in response to the mRNA from the COVID-19 vaccine gets blocked in your ACE2 receptor. This is because the new genetically modified spike protein has additional prolins inserted that prevent the receptors from closing properly, thereby causing ACE2 to downregulate. This is partly how you end up with problems like pulmonary hypertension, ventricular heart failure, and stroke. 9 , 10

As explained by Dr. Peter McCullough, 15 this means that after the first serum, your body will produce spike proteins for at least 15 months. But, when you are shot with no. 2 a few weeks later, that injection will cause peak protein production to continue for 15 months or more. With shot n. 3 six months later, make spike protein for another 15 months.

With regular boosters, you may never rid your body of spike protein. All the while, it’s wreaking havoc with your biology. McCullough likens it to “a permanent installation of an inflammatory protein in the human body” and inflammation is at the heart of most if not all chronic diseases. There is simply no possible way for these gene transfer sera to improve the health of the public. They will decimate him.

Long-term neurological damage is to be expected

In his article, 16 Seneff describes several key features of the SARS-CoV-2 spike protein that suggests it acts like a prion. This could help explain why we are seeing so many neurological side effects from the serums. According to Seneff, the spike protein produced by the COVID vaccine, due to the modifications made, could actually make it more of a prion.

COVID-19 serums are instruction sets for your body to make a toxic protein that will eventually end up concentrated in your spleen, from where protein-like instructions will be sent from the prion, radically increasing your risk of developing neurodegenerative diseases.

Lung, heart and brain diseases are predictable consequences

Seneff also goes into detail by describing how the spike protein created acts as a metabolic poison. Although I recommend reading the Seneff’s article in its entirety, I’ve pulled out a few key sections below, starting with how the spike protein created from serums can trigger pathological damage leading to lung damage and heart and brain disease 17

COVID sera activate latent viruses

As previously mentioned, herpes zoster infection is proving to be a rather common side effect of the COVID vaccine, and like the neurological, vascular and heart damage we are seeing, activation of latent viral infections has also been predicted.

One of the reasons latent viral infections are emerging in response to sera is because the injections disable the pathway of type I interferon. A second reason is because your immune system is overloaded trying to deal with the proteins flowing through the your body. Something has to give, so latent viruses can break through.

This isn’t the end of your potential problems, however, as these coinfections can worsen or accelerate other conditions, such as Bell’s palsy, myalgic encephalomyelitis, and chronic fatigue syndrome.

With all of this in mind, it seems inevitable that, in the long run, the COVID mass injection campaign will result in an avalanche of a wide range of debilitating chronic diseases.

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