Promoting the Formation of Stealth Adapted Variant Coronaviruses

Public Health officials seem not to ever realize the probable role of Covid-19 vaccines in hastening the introduction of stealth adapted coronaviruses. Indeed, they’ve still not accepted the presence of widespread human infections with stealth adapted monkey-derived viruses. These viruses were inadvertently introduced into humans from polio vaccines. This occurred since the consequence of using polio vaccines grown inside cultured kidney cells of cytomegalovirus infected monkeys.

A faulty assumption is usually that the current Covid-19 vaccines provide immunity that may be comparable to that regarding natural infections. This is clearly not. First, the vaccine emerges by intramuscular injections, whereas natural infections occur through respiratory mucosa. Intramuscular injections are certainly not particularly effective in stimulating the introduction of mucosal immunoglobulin A (IgA) antibodies or resident cytotoxic T lymphocytes (CTL). The lowered degree of vaccine induced mucosal immunity signifies that upon contact SARS-CoV-2 virus, a proportion of vaccinated individuals will almost certainly acquire a persisting, subclinical infection which is restricted to your superficial respiratory mucosa. Public Health authorities allude for this possibility by insisting those who are immunized will likely need to continue wearing masks. The persisting low-level infections will, however, supply the opportunity for your emergence of virus variants. Some of these could be more infectious, while other people will be better capable to evade vaccine evoked immunity and, therefore, you have to be widespread through the entire body.

The second major difference between the vaccine and natural infection is FDA’s allowance with the use of one particular virus component inside vaccine, namely the spike protein. It is easier for virus modification, or perhaps deletion, of 1 component than for concurrent changes to occur from the multiple antigens targeted by immunity to natural infections. Deletion on the spike protein can be done since coronaviruses have other way of entering into cells. The virus may then more easily undergo changes inside the remaining genes that code for that relatively few virus components typically targeted by cellular immunity.

The persistence of subclinical infections due to relative absence of mucosal immunity achieved by intramuscular injections along with the systemic immune response being on a only the spike protein, usually leads more rapidly than will natural infection, for the formation of stealth adapted coronaviruses. A corollary in this premise would be that the English, South African, and Brazillian variants probably started in individual participants with the Covid-19 vaccine trials conducted in each in the countries. With wider vaccine use, much more variants, including stealth adapted coronaviruses, have to be expected.

Stealth adaptation has another very concerning feature. It is the incorporation of more genetic sequences which might be probably required for that virus to regain infectivity. The added sequences comes from the cellular genome and from your genomes of other microbes. This has, for instance, allowed polio vaccine derived stealth adapted viruses to create monkey cellular sequences into humans.

The mental abilities are particularly subject to symptomatic illnesses a result of stealth adapted viruses. These viruses could be cultured from patients with all the chronic fatigue syndrome (CFS) and in addition from children with autism. The Long Covid syndrome has numerous clinical features that resembles CFS. Until proven otherwise, the Long Covid syndrome might be of interest as a viral illness with all the potential of human to human transmission, including when pregnant. It is critical to begin culturing blood samples from patients together with the Long Covid syndrome as well as sequence any resulting viruses.

Although the cellular disease fighting capability will normally not engage stealth adapted viruses they’re able to still be suppressed through alternative cellular energy (ACE) pathway. This pathways has likely preceded photosynthesis in plants as well as the obtaining of one’s by all life forms through the metabolism of food. In humans and animals, the mental faculties are probably the major receiver from the life-force energy for your ACE pathway. The attracted energy will then be transferred to your body’s fluids where it truly is expressed being an added kinetic activity. The energy is termed KELEA, an abbreviation for Kinetic Energy Limiting Electrostatic Attraction. KELEA may also be added to water, which will then be termed KELEA excellerated water. Wearable pouches containing this water and inhaling nebulized mists on the water are increasingly being evaluated as simple methods of enhancing the ACE pathway. These approaches can seemingly suppress both conventional and stealth adapted virus illnesses.

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