I’ve taken a lot of heat and even been censored for publicly announcing that none of the shots called vaccines can provide any protection of infection, nor can they stop the spread of viruses. I’ll get more flack for writing this preamble, but I welcome it. I am willing to openly discuss any of this any time anywhere with anybody.
Here is the truth: All these shots have one goal: create antibodies. Antibodies also have one goal: REACT to an infection. Antibodies created from shots are called serum antibodies, because they are always INSIDE of you, circulating in your blood and lymph. The only time these antibodies can do anything for you is AFTER you have become infected, and the virus is INSIDE of you. They cannot stop a virus from getting from the outside to the inside. I hope this is not too confusing, but there is one type of antibody than CAN stop viruses from getting inside of you. This is called a secretory IgA antibody because it is secreted from the inside of you to the outside, into your mucus membranes, and can disable viruses before they can get in. But secretory IgA can only result from natural infections coming through the mucosal lining, never from a shot that bypasses that mucosal lining and injects the virus, part of the virus, or the message to make part of the virus directly inside of you.
The true protection of infection is provided by something called your INNATE IMMUNE SYSTEM. The innate immune system does not rely on antibodies. It firstly relies on the mucus that covers the epithelium, the barrier separating the inside of you from the outside of you. It is very difficult for viruses to get through this mucus. In fact, there are tiny hairs called cilia buried in the mucus that constantly sweep viruses, bacteria and other stuff toward your mouth and nose so that they can be coughed, sneezed, or spit out into a tissue that can be thrown away, not into a filthy rag strapped to your face all day so that you can rebreathe that crap, Fauci. And the mucus naturally contains small amounts of hypochlorite and hydrogen peroxide that can oxidize viruses. Viruses are not living things and cannot be killed, only disabled, dismantled, or destroyed. If allowed to remain intact, the viruses can be accepted by the cells of the epithelium to make more copies of the virus. The copies of the virus can be released inside of you, and this is called a viral infection. Some copies can also be released back to the outside and into the mucus where they can be transmitted to other people. It is important to know that the virus is not controlling any of the replicating, your cells are doing it. Mutations or variations can happen during the replication process and your body is intelligently controlling this also through the actions of APOBEC enzymes. Viruses do not have the ability to copy themselves nor mutate themselves. You can learn about APOBEC here: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7760323/
If viruses do manage to filter through the mucus, there are receptors on cells that form the epithelium that can attach to the viruses. This is all happening before you are infected. The viruses are not controlling any of this, the intelligence within your body is controlling it. If the cell attaches a virus, the instant this happens, the immune system of your body knows it and will begin to act.
The next thing that can happen is a merge between the capsid or shell of the virus and the cell membrane. This will allow the genetic contents of the virus to enter the cell. The cell is accepting the virus, the virus is not injecting itself nor its genetic material as it has no intelligence, nor the ability nor the desire to do that.
The virus and/or its genetic material are now inside the cell of the epithelial barrier, but you are not infected yet. We are now deeper into the protection of infection provided by your innate immune system. There are specialized sentinel cells that patrol the epithelial barrier and keep you from becoming infected. There are many, but we’ll talk about three of them, natural killer cells, dendritic cells and activated T-cells.
Natural Killer cells or NK cells can recognize cells of the epithelium that have viruses inside of them. This is because cells normally display what is called an MHC1 site on their surfaces. But when cells have viruses inside of them, the MHC1 disappears for a while. In a normal healthy unjabbed person, the NK cells will recognize this and destroy the epithelial cell and the viruses inside of it BEFORE the viruses are released and infection happens. That is prevention of infection. And the beautiful thing about this is, the NK cells does not care what virus it is. It could be Sars-CoV-2, Marburg, Ebola, or a man-made viral particle…it does not matter. You can read about how that works here: https://www.nature.com/articles/nri1603
The dendritic cell is shaped like an octopus and can reach through the fence, grab the virus on the outside, bring it inside of itself, chop the virus up into all its protein parts and show these parts to other cells of the immune system on the inside. Some of these cells on the inside are T-cells, and if they recognize any parts of the virus, they become activated or cytotoxic. This gives them the authority to destroy the cell with the virus attached to it or inside of it BEFORE the infection occurs. The marvelous thing about this is, they can cross-react to similar viruses they have dealt with before. We know this happens because stored blood samples taken from people before the Sars-CoV-2 virus was even identified had T-cell memory that was able to recognize it. Read about that here: https://www.nature.com/articles/s41598-021-92521-4
The sad thing is that if you got the Covid-19 jab, the cells of your innate immune system can be depleted: https://www.nature.com/articles/s41421-021-00329-3 This makes you more susceptible to not only infection by the Sars-CoV-2 virus, but all viruses. This will make it impossible to reach herd immunity. Herd immunity is reached when enough people have innate immunity that PREVENT infections from happening and therefore spreading to others. People who got the shot will always be more susceptible to becoming infected. The only way to herd immunity is for enough of the population to remain free of the shot, keeping their innate immune systems intact so that they can not be infected in the first place.
It is also possible to reach herd immunity by allowing natural infections to occur. This will allow training of naïve T-cells to recognize and prevent infections from variants. This is not possible with injecting the message to make just the spike protein part of the virus, because the antibodies created as a result are too numerous and too specific and will allow infections of variants.
So, what are these shots called vaccines supposed to do for us? The idea is that after injection of an infection by a shot called a vaccine, reaction to subsequent infections will be provided by the ADAPTIVE IMMUNE SYSTEM. It’s called adaptive because it adapts to the infection, does not prevent it from happening. All antibodies are part of the adaptive immune system, even secretory IgA antibodies. Again, the secretory IgA is the only antibody that can prevent an infection, but it can only by created by reacting or adapting to a previous NATURAL infection, not an injected infection. There are also antibodies we were born with called innate or natural antibodies. They are called innate because we were born with them, but they can not prevent an infection, only react to it once the viral antigens are in the blood or lymph. These innate or natural antibodies are special because they are less specific and can react to various viruses, not just one.
Antibodies are important because the next time you get infected by the virus, and you will, they can react quickly and reduce the duration or severity of symptoms. The memory to quickly remake the antibodies is most important because antibodies almost always disappear from the blood over time. A collection of symptoms is called a disease. So, there is some protection of disease provided by serum antibodies, but never protection of infection. But the match between the antibody and the antigen must be perfect. Our bodies have mutated the spike protein on the original Wuhan virus. The mRNA in the shot is modeled after the original spike protein which no longer is prevalent. So, people who get the shot are making antibodies that don’t work. Worse, these crappy antibodies can enhance the ability to become infected by variants. We’re seeing this happening now as many fully injected people like Fauci himself are getting covid symptoms.
Why are these basic concepts so important? Because the narrative coming from your government has many of you convinced that injecting yourself with something called a vaccine can protect you or others from getting infected and spreading an infection and get us all to herd immunity. This is impossible as you now know. But it’s worse than that because they have many people convinced that they need to get booster shots to raise the level of antibodies. It’s the memory to make antibodies that is most important, Fauci, not the antibody titers. And every time you load yourself with another booster, you weaken the innate immune system even more. Continuing down the road of pumping booster shots into the population will be devastating to the health of our nation.
Excellent report. Thanks for writing!
Hi Kevin
I’ve an alternate explanation for why colds and flu are seasonal. You may like to read and ponder my articles. They bust a few paradigms.
What causes a cold or respiratory dis-ease?
The establishment’s model of blood and lung physiology fails under scrutiny. I’ll explain why.
We breathe air not oxygen.
Air is measured by its moisture or humidity Eg its at 45% humidity today
Oxygen is measured by its dryness Eg medical oxygen has 67parts per million or less of water contamination.
The lung alveoli requires air reaching it to be at 100% humidity, that is dew point.
Can you comprehend the mis-match?
Oxygen is manufactured by stripping air of moisture. Oxygen is a product of air NOT a constituent of air.
There is no wild/natural oxygen in air. Oxygen becomes nitrogen with the addition of carbon particles to become a non-flammable version of oxygen. I have a link to a demonstration of this on my stack, a home oxygen concentrator is used.
The lungs are responsible for re-hydrating the red blood cells as they pass through the alveoli capillaries with salt water. The red blood cells are salt water sponges.
The saline intravenous drip rehydrates red blood cells and aids the lungs.
The insult that causes respiratory dis-stress is dehydration. It’s seasonal because cold air holds the least moisture and indoor room air often dries out with heating.
The dry mucosa must re-establish itself and the production of mucus goes into overdrive. The mucosa requires salt and moisture and it will move both from any bodily reserves. This causes pain as the extraction process goes into motion.
Now you know why the old remedies are successful.
Salt water gargles, nasal irrigations/inhalations and chicken soup / bone broth soups.
Sanatoriums were built along coastlines to take advantage of sea spray because it was known to heal injured lungs.
It is time the COMMONS reclaimed the knowledge of hydration and healing.
Hydration equals salt plus water.
Healing begins with hydration.
Oxygen’s toxicity is directly related to its power to dehydrate. Reactive oxygen species ROS describes damage due to dehydration.
Oxygen on release from a container will extract moisture from its surroundings to become air, its natural state. Oxygen released inside the respiratory tract extracts moisture from the mucosa and the delicate alveoli causing dehydration. This can kill.
Oxygen is a prescribed drug. It is primarily prescribed for the terminally ill. Palliative care is not kind.
We all need to comprehend the difference between air and oxygen.
Read the material safety data sheets for oxygen and nitrogen. Both have unconsciousness and not breathing listed under inhalation.