My Views on Shedding

...and the various forms of it

Traditionally the term shedding applies to an infected person transmitting the virus particle to another person. This can happen when the shed particle is accepted into the cells of the epithelium that separates the inside of you from the outside of you. If the particle is copied by the cell and released, some go into the blood and lymph, and now you are infected. Some go back out into the mucosa of the epithelium so they can be coughed, sneezed, or breathed out into the atmosphere. In the atmosphere, some will become aerosolized and will be inhaled by others, whether or not they are wearing masks.

That is a description of viral shedding or transmission, but do not be afraid of this. It is happening all the time and you cannot stop it any more than you can stop ocean tides. I recognize that some people, even some doctors do not believe viruses exist. That’s fine, but it cannot be denied that unique genetic material can be found in people with or without symptoms. That unique genetic material moves around between us for sure, it’s the method of how it moves that is debatable. Some say it is a particle, some say no. I’m in the camp of yes, it’s a particle. Which brings us to the concept of asymptomatic transmission. Yes, there is asymptomatic transmission of genetic material between humans all the time, but not transmission of symptoms. Whether you will display symptoms or not is dependent on the condition of your immune system.

Concerning the covid-19 disease and the covid-19 shot, there are many things that can be transferred from one person to another. These include the Sars-CoV-2 virus and all its variants, exosomes, and recombinant viruses that can make the spike protein. It might also be possible to shed spike proteins or lipid nanoparticles. We’ll go over each one, just remember that they must get inside of you to have any effect. And when I say inside of you, I mean in your blood or lymph. I do not mean stuck in your snot, spit, or the mucosa of the gut lining. All those mucosal locations are outside of you. That fact alone was responsible for most of the fear and panic because just about anyone, including your dog or cat, can test positive for the viral genetic material in the snot, without being infected.

Most of the shedding is the complete virus particle coming from people who got injected. In fact, all entities involved in the distribution of the shot have admitted that it cannot stop infection, nor can it stop transmission. How can this be? Because the protection of infection is cellular, and those immune cells got retrained to look for the spike protein created by the shot, not the spike protein that exists on the mutated viruses in nature. Therefore, the injected will continue to be infected by variants. Here is “Shedding of infectious SARS-CoV-2 despite vaccination”: https://pubmed.ncbi.nlm.nih.gov/36178969/ Do not fear this shedding. People who are un-injected will have cellular protection of infection and should not be concerned by the shedding of these virus particles. A few un-injected people may be susceptible to symptoms after being exposed to shedding if they are immunosuppressed. Most people affected by shedding are the injected because they have lost the cellular protection and will continue to reinfect themselves.

Another possibility is transmission of exosomes. It is known that exosomes are secreted by cells and these exosomes can contain genetic material capable of making the spike protein, or fragments of the spike protein that can be toxic. Most of the research on exosomes has confirmed that they are secreted from tissue cells inside the body, stay inside the body, and are involved in intercellular communication. However, it is possible that exosomes can also be secreted by epithelial cells back out into the mucosa and transmit horizontally between humans. This study mentions exosomes can be detected in blood, urine, exhaled breath condensates, bronchoalveolar lavage fluid (BALF), and other fluids. https://pubmed.ncbi.nlm.nih.gov/29311962/ It is also possible for exosomes to transmit vertically through generations. This was first discovered by veterinarian vaccinologists investigating chickens. https://www.frontiersin.org/articles/10.3389/fimmu.2021.735280/full

Another possibility is novel viruses assembled in human cells due to genetic recombination and becoming transmissible. Some people call these “Frankenstein viruses”. Simply put, our cells are protein manufacturing centers. They are constantly making proteins. Just because a cell takes in the mRNA from the shot and starts making spike proteins, doesn’t mean it stops everything else it is doing and just makes spike proteins. It can be dealing with other RNA from other viruses. Under the right conditions, RNA fragments can combine. The message to make the spike protein can get incorporated into the genome of another virus that could be replicating inside the cell. Now you’ve got a new transmissible particle capable of making the spike protein. It will still show a positive PCR test result because those small nucleotide sequences the PCR detects will still be there. Unless a complete genome is sequenced, you will never know if it was a brand-new virus or not.

Shedding of Sars-CoV-2 virus variants, exosomes, or novel viruses capable of making spike proteins will only affect people who are vulnerable to infection, certainly not everyone. And the symptoms would take days to manifest. But some people report physiological changes almost immediately after being around injected people. So, something else could be happening.

Some say it is the spike protein that is shedding and affecting others. I disagree. Remember, the spike proteins are made by the cells of people who get injected with mRNA and released into the blood or lymph as toxic proteins. The body will try to eliminate these toxic proteins through sweat, breath, and other excretions. If you breathe them, swallow them, or touch them, they must get in you, past the epithelial barrier to affect you. If you breathe them or swallow them, they can either attach to receptors, or they might be able to sneak into the blood through abnormal breaks in the mucosa. If they attach to receptors, they will just sit there, blocking them, unable to get into the epithelial cells. If they do get past the epithelial barrier through a leaky gut or breaks in the mucosa, there is no ability for them to make more of themselves, so unless tons of them get in, not much is going to happen. Remember, it’s the mRNA that makes the spike protein, the spike protein cannot make more of itself. So, perhaps it is the lipid nanoparticle that contains the mRNA that makes the spike protein that is shedding.

It's important to know that the lipid nanoparticle (LNP) that is injected is a lipid shell about the same size as the Sars-CoV-2 virus, about 100nm or .1 microns. Inside of those lipid shells are many smaller lipid nanoparticles that contain the mRNA. They are about a tenth of the size of the big one. The big particle is made of normal body fats, cholesterol and DSPC, explaining why it is readily accepted by the body and goes everywhere. The big LNP merges with cell membranes, and the smaller LNPs will get into the cell. Under the right pH conditions, the smaller LNPs will release the mRNA into the cytoplasm for spike protein production.

The smaller LNPs that contain the mRNA are proprietary. Pfizer’s is called ALC0315. Moderna’s is called SM102. They are toxic. The mRNAs inside of them are proprietary also. Pfizer’s is called Tozinameran and Moderna’s is called Elasomeran. They are not the same, so the proteins they make are similar, but not the same. Nor are they the same as what was on the original Wuhan virus. That fact alone should have been a red flag at the start.

When the large LNPs are injected, not all of them will merge with cells. Some will eventually break down and allow the smaller toxic ALC0315 or SM102 LNPs to circulate in the blood and lymph. A Danish study found circulating mRNA up to 28 days post injection. Here’s the link to the study: https://onlinelibrary.wiley.com/doi/10.1111/apm.13294 It was assumed that the mRNA they found was still inside the LNPs, otherwise it would have broken down. The big question is, can these circulating toxic LNPs that contain mRNA be excreted or exhaled and transmit from the injected to the un-injected? If so, this could explain why some people become symptomatic almost immediately after being around injected people.  

Pfizer was worried about exposure of people to trial participants. Here is the link to a few pages about exposure protocols: https://lcaction.org/LCA-PDFs/2021/Pfizer_C4591001_Clinical_Protocol_Nov2020-short.pdf It seems they were concerned about exhalation and skin contact. All trial participants were instructed to use contraceptive devices. Any female who was exposed to any trial participant by exhalation or touch and was pregnant or became pregnant had to report it. Further, any male who was exposed to a trial participant by inhalation or touch, and then impregnated a female had to report it. The pregnancy had to be tracked with descriptions of the appearance of the fetus if the pregnancy was terminated. Also, if the newborn died, it needed to be reported as a significant adverse event due to environmental exposure. Additionally, any female who was breastfeeding and encountered a trial participant by inhalation or touching had to report it. It goes on to say that any person who has unplanned direct contact with a trial participant must report it as an “occupational exposure”, whether or not an adverse effect was evident.

Why so much concern about contact with trial participants? Because they are using a vector (lipid nanoparticle) to deliver gene modification. Anytime you use vectors to deliver gene modification you put others at risk if they come in contact with the vector.