Go ask Alice, when she’s ten feet tall
For a tiny virus inducing an illness very similar to and no more serious than influenza, that 98% of people survive an encounter with, that actually belongs to the same family that makes up 10% of the viruses that cause influenza, it is no mean feat for it to have cancelled civilization.
It would seem that the reason for this overblown and disproportionate response has been to drum up the artificially perceived necessity for global mass “immunization” by means of a new generation of untested “vaccines”. These “vaccines” thus far, foisted upon the world with such inordinate haste, have been equally overblown in terms of their purported efficacy.
The official narrative bleats perpetually that only a particular kind of medical intervention can save humanity from this new plague. The financial and political advantages of such an intervention that will accrue for the ruling class of oligarchs does not come into this story. The engineered solution is tailor-made to fit the contracted version of the reductionist approach to medicine, what Dr Shiva Ayyadurai calls the “Two-box model.”
This model is reduced to two components, the Innate and the Adaptive immune systems.
Both these systems rely on an army of immune cells, called white blood cells or leukocytes, located in the eyes, nose, throat, skin, blood and lymphatic systems.
The innate system is composed of specialised white blood cells called phagocytes. These, like soldiers dealing with foreign invaders, attack pathogens in a non-specific manner, leaving behind antigens.
The adaptive system uses white blood cells called lymphocytes to make antibodies, specific proteins to fit the antigens, helping the body to remember and recognise the invaders. Lymphocytes are made up of B lymphocytes and T lymphocytes. B lymphocytes are like the body’s military intelligence system — they find their targets and send cells to lock onto them. T cells, or “killer cells”, are, in the military analogy, like “sharpshooters.” They destroy the invaders that the intelligence system finds and targets with antibodies. T cells also signal the phagocytes to lock onto their targets. The antibodies remain in the body and the body remembers how to make them should they be required in great numbers.
It is important to note that the immune system not only neutralizes foreign microorganisms but also poisonous or damaging substances and even the body’s own cells that are infected, or poisoned or run-down with old age.
In the two-box model, it is viruses that pose a particular challenge to our innate and adaptive immune systems by dint of their tricky nature. In this reductionist view, it is Sars-Cov2, the novel Coronavirus, that is at the apex of tricky evolution.
Coronaviruses get their name for the three-dimensional crown of spikes that has made one particular Coronavirus notorious. These spikes are proteins – spike proteins that act as the key for the locks – the ACE-2 receptors of the cells they are attempting to enter, the host cells.
When a virus effects an entry into a cell, it releases RNA. This viral RNA uses the ribosomes of the host cell to create new viral RNA. It replicates itself. This new viral RNA then assembles new viral particles which leave the cell to enter new cells.
Once inside the host cell, the immune system cannot “see” the virus. The innate immune system cannot recognize a virally-infected cell. The adaptive immune system can only recognize such a cell when the cell itself presents pieces of proteins, the antigens, on its surface. In this case it will be the spike protein or a fragment of it. The B cells will then form antibodies to fit the antigen so that they can neutralize viruses before they enter cells leaving the phagocytes to mop them up. The adaptive immune system also signals for the T cells to kill the body’s own cells already infected with the virus. The T cells have special protein receptors on their surfaces to help them recognize virally-infected cells and kill them by using cytotoxic factors to enter and trigger cell death – apoptosis. These cytotoxic cells also produce and release proteins called cytokines, which enhance the killing mechanism in other infected or neighbouring cells. These proteins are of major significance as we shall see.
Outside the Two-boxes
The two-box model of the innate and adaptive immune systems and their antibody response is the basis of vaccines.
However, as Dr Shiva Ayyadurai tells us, this model is incomplete. When scientists widen their gaze, they see the two-boxes as complex systems inter-related with other complex systems within a larger, encompassing system. This approach yields the Systems Architecture of the Immune System.
All these systems are in communication with the neural system and gut-brain axis. They work together to maintain homeostasis.
The Interferon (IFN) system
Integrating between the two-boxes we have the missing link, the Interferon system. The interferons are proteins manufactured by the genetic system within virally infected cells and defend against a whole host of viruses by directly interfering with their ability to replicate within an infected cell. In addition, they function as signalling molecules enabling infected cells to warn neighbouring cells of a viral presence by increasing the numbers of receptors known as MHC class I molecules upon their surfaces, so that T cells on patrol can identify and neutralize the viral infection as outlined above.
The Microbiome and Virome
Augmenting and interlocking with these systems are the 60 trillion bacteria that make up the biome and the 380 trillion viruses that make up the virome throughout the 6 trillion cells that make up our human body. Throw in a few fungi and we have a walking, talking eco-system.
It is a misconception to view all viruses as hostile invaders. In fact, harmful viruses like harmful bacteria, are in the minority.
Professor Higa, an expert in microbiology, found that within the world of microorganisms, 10% are harmful. However, there are also 10 percent of beneficial microorganisms, the angels in the architecture. There is an ongoing power struggle between the beneficial and harmful microorganisms. The remaining 80 percent he refers to as “wait-and-see” microorganisms. They watch until either the good or the bad microorganisms emerge as the victors, and they join the stronger of the two and imitate them.
One is reminded of the old Cherokee story of the old man who tells his grandson of the two wolves fighting inside his heart, one evil and the other good. When asked which of the wolves will win, he replies that it is the one he feeds.
Ultimately, it is not even the “harmful” virus that harms or kills us, rather it is the overreaction from a weakened and dysfunctional immune system to the presence of the virus that results in the body attacking its own cells, tissues and organs.
In a weakened and dysfunctional immune system, the body overreacts. Cytokines are produced in excessive quantities from the innate and adaptive immune systems and their subsystems. These signalling protein molecules induce an overwhelming influx of various immune cells that destroy cells, tissues and organs.
The Coronavirus family has a preference for the epithelial tissue of the lungs. During a Cytokine storm, the immune system attacks the epithelial cells in the lungs in a vain attempt to rid itself of the viruses that dwell there. This brings on the respiratory distress syndrome as the epithelial cells are damaged, the alveoli fill up with fluid and gas exchange is drastically impaired. The conventional response to this has been to put the patient onto a ventilator which further increases pressure on the lungs and increases the chance of death significantly.
Boosting the Angels in the Architecture
As Dr Shiva tells us, the dysfunctional immune response arises from underlying pre-existing conditions such as obesity, diabetes, heart disease, smoking and from those who are immuno-compromised, such as the elderly. The environment, both inner and outer contributes to the dysfunctional immune system though such factors as polluted air, water and food.
According to Dr Shiva, the immune system thrives on the right kind of stress, termed “Eustress” by Hans Selye. It needs continual inoculating with germs in order to activate all its various sub-systems and become resilient. Recovering from an infection confers long-term immunity. Vaccination does not. This is because the immune system has two branches — the cellular (T-cells) and the humoral (B-cells). Both need to be activated for long-term immunity to be secured. A vaccine only stimulates the humoral immunity, the B-cells. The T-cells are not stimulated.
This is why the prevailing doctrines of isolation, mask-wearing, social distancing and immunization fly in the face of this expanded logic. These policies cause the immune system to steadily atrophy. Nor do they protect the immuno-compromised. Those with weakened and dysfunctional immune systems require boosting, but not through vaccination.
This can be achieved though work on the environmental factors described above, air, water and food. The internal environment can be influenced through sufficient sleep, exercise, meditation and optimal mindsets. One should never underestimate the importance of social relationships in boosting immune health and lowering inflammation. The field of Psychoneuroimmunology has shown that happy thoughts, an optimistic attitude, laughter and love in relationships generate very powerful chemicals that support the immune system. The opposite occurs from social isolation where harmful compounds are produced and genes that code for immune function and inflammation are impacted negatively. It has been found that lack of social connection is of greater detriment than obesity, smoking and high blood pressure. Strong social connections, in contrast, confer a 50% increased chance of longevity, a more resilient immune system, and swifter recovery from illness.
Immune system resilience can also be enhanced through the use of truly effective “pills” such as:
Vitamin D3, which is actually a hormone, along with Vitamin K2 and magnesium, has been shown to boost the immune system to the extent that it cuts the likelihood of Covid ICU admission rates by 25 times and eliminates deaths altogether. Supplementation of Vitamin D3 has been established as safe, although it is also produced from exposure to sunlight. Winter and lockdown reduce Vitamin D3 production drastically. A Spanish study found that 80% of Covid patients were deficient.
The lower the levels of Vitamin D3 in the blood, the greater the levels of coronavirus infection. In Great Britain people have been found on average, to have 4-6 times lower than optimal levels of Vitamin D in the blood. Such deficiency is a primary risk factor in infection, hospitalisation, complications and death.
Vitamin D3 has been shown to:
- reduce the survival and replication of viruses
- create a chemical called Cathelicidin Antimicrobial Peptide (cAMP). These proteins disrupt the walls and cells bacteria and viruses. This is the oldest mechanism of action towards microbial pathogens.
- reduce inflammatory cytokine production,
- maintain and repair endothelial integrity,
- increase angiotensin-converting enzyme 2 (ACE2) concentrations, which prevents the virus entering cells via the ACE2 receptor,
- boost overall immune function,
- improve lung function and reduce respiratory distress,
- help production of surfactants in lungs that aid in fluid clearance,
- and lower risk of comorbidities such as obesity, Type 2 diabetes, high blood pressure and heart disease.
Just the simple administration of 6,000 to 8,000 IU per day over several weeks could have profound effects.
Compare the “efficacy” of the vaccine – 1 in 256 recipients receiving the dubious benefit of not constituting a “case” where we don’t even know the cycle threshold of the PCR test used to establish that “case” and have no information on hospitalisation and death rates, with that of Vitamin D3 – cutting ICU admissions by a factor of 25.
Compare the media attention that the vaccine has received with the blackout and censorship that the benefits of Vitamin D3 has received.
After this there is no turning back.
It is complications of Covid infections resulting in pneumonia and SARS, the severe acute respiratory syndrome, that kills people. Most people will have a mild case. Some will have the virus with no symptoms at. It is unknown how many of these people there are because they have no symptoms.
Vitamin C has been known to be effective against viral pneumonia since the 1940s when Dr Frederick Robert Klenner published a series of papers and was able to reverse viral pneumonia in 72 hours. His work is conspicuous by its absence in the reporting by mainstream media.
- Increases cellular immunity in white blood cells, neutrophils, macrophages, and lymphocytes. White blood cells carry lot of vitamin C and this is used up rapidly during viral infections.
- Increases humoral immunity (B cells, antibodies).
- Increases antiviral proteins (Interferon).
- Increases energy by providing electrons and electron movement for mitochondrial ATP generation – respiration.
- Disrupts viral replication
- When applied in large enough doses, limits sugar – the fuel for pathogenic organisms.
- Maintains structural integrity of cells by enhancing collagen formation.
- Scavenges virus-induced oxygen free radicals and restores other cellular anti-oxidants.
- Inhibits activation of pro-inflammatory cytokines.
A South Korean doctor who, during the first wave, was giving patients and hospital staff 100,000 IUs of vitamin D and 20 to 24 grams of vitamin C by IV, reported virus-infected patients were recovering in a matter of days.
Dr Shiva states that while mega-doses, from 50,000g to 100,000g during medical emergencies can be life-saving, they are not necessary for everyday use. Around 2000mg per day, spread out in 500mg doses 4 times a day, is recommended for those who wish to maintain a robust immune system. Studies have shown that even 200 mg of vitamin C a day will reduce the death rate in elderly people with severe pneumonia by 80%. The mortality goes down and the duration and severity of the illness is less.
Much of the information about vitamin C during the coronavirus has been coming out of China. Dr Richard Cheng, a Chinese American physician was in Shanghai for the Chinese New Year visiting his family when it all began. He stayed on and advised hospitals and Chinese physicians to use vitamin C as both a prevention and cure. They showed great interest to the degree that the government of Shanghai issued official recommendations that vitamin C should be used for treating COVID-19. They then proceeded to run three studies on using high-dose vitamin C as therapy, focusing on people in intensive care. The Dutch State Mines or DSM of the Netherlands even donated 50 tons of vitamin C to Wuhan.
However, in the west, a lot of this nutritional advice is being censored and marked as “fake news” to the extent that Dr Cheng had a video, where he covered Vitamin C case reports, removed from YouTube. A flurry of desperate articles came out attempting to discredit the claims of Vitamin C being beneficial, ignoring the thousands upon thousands of studies backing such claims. This did not deter Doctors in New York, operating in a bottom-up manner, from treating their patients successfully with Vitamin C.
The mineral zinc inhibits viral RNA replication. Preliminary research found COVID-19 patients with plasma zinc levels below 50 mcg/dl at admission had a 2.3 times greater risk of in-hospital death than those with a zinc level of 50 mcg/dl or higher.
However, it is poorly absorbed and requires molecules to help it transport across cell membranes.
Zinc ionophores act as gates for zinc to pass through the cell membrane allowing more zinc to enter cells and inhibit viral RNA replication.
Examples of zinc ionophores include:
- Epigallocatechin-gallate (EGCG)
Iodine and Potassium Iodide.
These two enable the production of Vitamin A in the thyroid.
- Produces cytokeratin
- Protects epithelial tissue from scarring
- Enhances macrophage and T cell activity.
Like the cake that enables Alice to outgrow her former size and hit her head on the ceiling of the room she is in, the expanding awareness of the systems architecture of the immune system can no longer be contained within the rudimentary 100-year old model. The purveyors of the contracted view will do their utmost to prevent you learning this.
Yet the purveyors have never before sunk to such depths as they have in promoting their perverted vaccine narrative and agenda.
This will be the focus of Part 4.