SARS/Covid-19 is an RNA virus, this means that the genetic code for the virus is carried on RNA not DNA. This is significant. It also means we’re going to review some cellular biology so you can understand better what we’re talking about. Don’t worry–no test at the end!
I’d like to state at the beginning of this article that I am “pro-vaccine”. Vaccines have done a lot to reduce the burden of illness in the human population. Unfortunately, there are risks as well as benefits with vaccines as with so many different things in life. Vaccines contain inherent toxicities, maybe you’ve heard of thimerasol which contains toxic mercury which a highly toxic adjuvant (agent that increases vaccine effect).
Giving to many vaccines at once can also over-tax the immune system. Think of a vaccine as you would a knife–useful for preparing food–but you might cut yourself!
Table of Contents
- 1 RNA Viral Replication
- 2 How DNA & RNA Structures Function;
- 3 How Enzymes Such as Transcriptases Function;
- 4 Review of RNA & Protein Synthesis;
- 5 Genetic Engineering
- 6 Viral Replication
- 7 Viral Mutations & Shared Genetic Information
- 8 COVID19’s Transcription Twists
- 9 Function of a Vaccine;
- 10 Vaccine Issues
- 11 Antibody-Dependent Enhancement of Covid
- 12 Covid Morbidity & Mortality
- 13 Graphics provide interesting insight into Covid19 as of December 2020
- 14 Pandemics; Swine Flu in 2009, Covid19 in 2020 Compared
- 15 Concerns Regarding the Covid19 Vaccine:
- 16 Australia Scraps Covid-19 Vaccine That Produced H.I.V. False Positives
- 17 This Document Would be Incomplete Without Mention of Other Issues;
- 18 So; What Should We Do Regarding this Covid19 Vaccine?
The coronavirus RNA genome has a 5′ methylated cap and a 3′ polyadenylated tail, which allows it to act like a messenger RNA (mRNA) and be directly translated by the host cell’s ribosomes. In a sense, it’s acting like human mRNA.
The DNA “Alphabet”
Ribonucleic acid (RNA) is a nucleic acid similar to Deoxynucleic acid (DNA) which is where the genetic code of “higher” organisms such as mammals reside. Both DNA & RNA like to “couple up” to become more stable and to make replication easier. Each strand can be thought of as having a “starting point” such as a 3′ polyadenylated tail and a 5′ methylated cap as mentioned above. The arrows in the image below demonstrate the 3′ tail with arrows drawn in which show the direction of transcription–or copying the strand. The base pairs for DNA are Adenine & Thymine which have an affinity or desire to match up with each other and Guanine and Cytosine which have similar characteristics–the language of DNA consists of 4 “letters” Adenine, Thymine, Guanine & Cytosine.
The RNA Alphabet
Similarly, RNA has 4 letters in it’s alphabet:
The RNA alphabet is nearly identical; the difference being one letter; Uracil replaces Thymine.
How DNA & RNA Structures Function;
Imagine a simple strand of DNA;
–>3′–>T–>G–>A–>C–> 5′ (Arrows represent the way in which the transcriptase
<–5′<–A<–C<–T<–G<–3′ enzyme moves, notice pairing of bases)
How Enzymes Such as Transcriptases Function;
If you see a biological term ending in “-ase” it’s a good bet that the term is naming an enzyme. Enzymes are special proteins that carry out chemical reactions with great specificity (few undesired chemical byproducts) and efficiency (speed). Enzymes are essential to life. “Transcriptase” similar to “transcript” enzymes simply copy. No great mystery–nothing to fear here! So pay attention class! These transcriptase enzymes work along the strand in one direction. Please notice above how there is a certain “directionality“, similar to reading the page in a book where we read left to right, for there to be a “matched” strand it would require that that particular strand be read right to left–this is important.
Sense vs. Anti-sense
So, looking at the above information, we can see that one side of this parallel string of nucleic acid base pairs conveys information–known as the “Sense” side, the other is only there to provide accurate copying, the “Anti-Sense” side. Typically of course, the “Sense” will convey that information from the 3′ to the 5′ direction only. It’s like reading a sentence from left to right (OK so far…) but then there’s another mirror of sorts of the sentence above it which can only be read right to left–you need to be reading the correct sentence and know which one is correct.
Transcriptase vs. Reverse Transcriptase
Transcriptase enzymes “read” from 3′–>5′ so the genetic copy being produced would be produced from 5′–>3′. If this isn’t complex enough, there are also enzymes called “reverse transcriptase” that, you guessed it, read from 5′–>3′ producing a copy from 3′–>5′.
Review of RNA & Protein Synthesis;
DNA provides the genetic information. That information is essentially “manifested” in the creation of proteins. DNA lengths that contain information to make a given protein are referred to as “Genes” which are present on “Chromosomes“.
Humans have 23 pair of chromosomes including sex chromosomes “X” & “Y”. Ladies have 2 copies of X, guys have an X & Y. The other 22 pair of chromosomes are known as autosomes.
If you stretched the DNA in one cell all the way out, it would be about 2 meters long and all the DNA in all your cells put together would be about twice the diameter of the Solar System.
Special proteins called “histones” have the ability to pack it together so tightly that it fits in the cell nucleus–we won’t worry about all that now though.
Messenger RNA (mRNA) carries the information from the “Sense” strand of DNA from the nucleus of the cell to the endoplasmic reticulum–a network fo special intracellular membranes containing ribosomes–intracellular organelles that “read” the messenger RNA and substitute certain amino acids for each 3 base pairs (triplet or codon). Each of our 21 amino acids has its own codon triplet. Special intracellular structures called ribosomes in the endoplasmic reticulum read each codon and plug the correct matching amino acid into the growing peptide chain.
THAT is how proteins are made.
Genetic engineering involves re-arranging genes and genetic expression. This process starts in the lab with figuring out what genes are responsible for an effect that change is sought. Then scientists look for a species with desirable characteristics due to a different copy of that gene. The desireable gene is spliced into the DNA and the resultant organism is evaluated for how well the gene is working. Using CRISPR technology it’s even possible to create novel genes by changing the base pairs of the DNA in a given gene. Of course, these “exciting times” don’t come without risks…
Viruses don’t have all the structures that our cells have. A virus is basically a small body made of nucleic acids–either DNA or RNA–both types of virus exist, a protein coat called a capsid and possibly an optional fatty “lipid envelope“, which among other things, help it to stay viable (able to be brought back to life) outside of living beings, say, on a countertop after somebody sneezes and the aerosol droplets of the sneeze evaporate.
The protein coat has receptors that recognize certain types of surface protein on our cells–the ACE2 receptor in our lungs works great from Covid19’s point of view–that’s how they gain entry into our cells, those proteins essentially have “keys” that match up to certain enzyme “locks” on the surface of our cells that gain them entry. Good for Corona, bad for people!
Once inside our cells, they essentially hijack our cells machinery to their own nefarious activities, killing the cell while making huge numbers of copies of themselves.
When a viral infection occurs, understand that it’s not only one virus per cell infected–numerous viruses can enter the cell simultaneously and all hijack the cellular machinery to reproduce more viral copies.
If there are multiple viruses from multiple sources, the viruses can also share genetic information amongst themselves while reproducing in the cell.
RNA viruses mutate faster than DNA viruses, single-stranded viruses mutate faster than double-strand virus, and genome size appears to correlate negatively with mutation rate.
Viral mutation rates are modulated at different levels, including polymerase fidelity, sequence context, template secondary structure, cellular microenvironment, replication mechanisms, proofreading, and access to post-replicative repair.
Additionally, massive numbers of mutations can be introduced by some virus-encoded diversity-generating elements, as well as by host-encoded cytidine/adenine deaminases.
COVID19’s Transcription Twists
A number of the nonstructural proteins coalesce to form a multi-protein replicase-transcriptase complex. The main replicase-transcriptase protein is the RNA-dependent RNA polymerase (RdRp). It is directly involved in the replication and transcription of RNA from an RNA strand.
The other nonstructural proteins in the complex assist in the replication and transcription process. The exoribonuclease nonstructural protein, for instance, provides extra fidelity to replication by providing a proofreading function which the RNA-dependent RNA polymerase lacks.
This is part of the mechanism a virus uses to “hijack” the cell’s resources to reproduce more viral particles.
Vaccines are usually composed of either an attenuated- weakened- germ or an isolated part of that germ. When introduced into the human body, it stimulates the immune system to form antibodies that recognize and fight against the introduced germ.
As an example, for the flu vaccine, we give pieces of the flu virus we break down the virus, separate out different parts of the protein component and inject them into folks we’re trying to protect so that their immune systems can make antibodies against the flu elements that were injected–thus giving their immune system an “education” on what the flu virus “looks like” so it’ll be “recognized” in the future. That’s the simplified version of course–it’s a bit more complicated than that.
The function of the antibody (Ab) is to bind to an antigen (Ag), which can be any component of the germ that needs to be defended against.
For purposes of simplicity the term “germ” can be a virus, bacteria, parasite, protozoan; ANY organism that would harm the host (person). Similarly whatever an Ab binds to will be known as an Ag.
The 5 major classes of antibodies are;
IgG–long-term memory–you want these as they store information on what infections your immune system has resolved in the past.
IgA–found in mucosal (moist) surfaces like GI, GU & Respiratory tracts.
IgM–Think of the Marine Corps–first to the fight, levels rise quickly then decline once an acute infection is resolved.
IgE–degranulates mast cells, involved in allergic and parasitic attacks.
IgD–fetal immunoglobin that declines and disappears after birth.
All of the antibodies share a common structure which is somewhat “Y” shaped as below;
The bottom of the “Y” is known as the Fc fragment–it binds to macrophages which essentially “eat” or engulf the germ that the antibody has attached to, killing the germ.
Accessory cells include the phagocytic cells (macrophages and neutrophils), which ingest antibody coated bacteria and kill them, and other cells—natural killer (NK) cells, eosinophils, basophils, and mast cells (see Fig. 1.4)—which are triggered to secrete stored mediators when their Fc receptors are engaged.
A key point to understand is that we can design vaccines to produce antibodies to the pathogen we want it to attack, BUT we cannot determine in advance how effectively the synthetically produced antibodies will work.
Will it bind tightly enough or lose it’s grip?
Will it bind to the accessory cell properly?
Will it neutralize any toxic effects of the antigen that it binds?
This will become clear as we move forward through this document.
Cytokines are a class of chemicals that are intercellular chemical messengers. We know that if we get a splinter in our finger, the area around the splinter will become swollen, red, tender–inflamed.
Inflammation happens because damaged cells release these chemical messengers which call out to white blood cells to come fight the local intruder (splinter, germs on the splinter, etc.)
The Complement Cascade
This is not a compliment (gee, nice outfit), it’s complement (completes a process). OK, why is it called a “Cascade“? This is another collection of proteins in the blood that are part of the immune system.
Think of a bucket of hand grenades with the pins pulled dumped into a room. They explode. They do a LOT of damage as they kill all of the “bad guys” in the room.
It’s a “cascade” because this chain of proteins work in a manner of A+B–>C, but not 1 “C” but say 10-100 of C, then C+D–>E, again, not one but 10-100 (or more).
So what we end up with starting with one of A & B, we gets tens of thousands of E, hundreds of thousands of F and so on exponentially.
Antibody-Antigen Complexes “Immune Complexes” can trigger this cascade, as can certain cytokines…
The vaccine has had very limited testing in humans. What happens if an RNA-dependent RNA polymerase is switched to a RNA dependent DNA polymerase that alters our genome–permanently?
If the vaccine is going to be so wonderful, why is there a movement among the UK, New Zealand, Australia, Canada & the US (The Five Eyes Alliance) to label anti-vaxxers as terrorist groups among these countries. Why would this group be labeled as terrorists for a vaccine that is supposed to be as wonderful as the press makes it sound?
Antibodies can actually worsen infection by two different mechanisms.
Impaired Antibody Neutralization of Antigen/Covid
Non-neutralizing or sub-neutralizing antibodies cause increased viral infection of monocytes or macrophages via FcγRIIa-mediated endocytosis, resulting in more severe disease. The macrophage engulfs the virus but is unable to kill the virus–the virus kills the macrophage instead.
Cytokine Activation & the Complement Cascade
For non-macrophage-tropic respiratory viruses such as RSV and measles, non-neutralizing antibodies can form immune complexes with viral antigens inside
airway tissues, resulting in the secretion of pro-inflammatory cytokines, immune cell recruitment and activation of the complement cascade within lung tissue. If Ab-Ag Immune Complexes are present in high amounts, the result can be unchecked inflammation. To much inflammation can be lethal.
Human endogenous retroviruses (HERV) such as Syncytin-1 and the Placenta
Syncytin-1 is a protein which is found in the “spike protein” of the Covid shell as well as in the human placenta. The vaccine is developed to bind to this “spike” protein (Syncitin-1) which is also present in the human placenta, sperm & egg.
If we develop antibodies to Syncytin-1, it can be good in that it will potentially stop the virus, however it will bind to any structure containing Syncytin-1 including human spermatozoa and egg cells & placenta. It will cause anti-reproductive cell antibodies, antibodies that will attack and destroy the reproductive cells, which should lead to permanent infertility.
Will that happen?
Well, let’s review the testing of the virus–oh wait, there hasn’t been the usual extensive testing–it’s pretty much untested.
We don’t KNOW what will happen! As a biologist, I do however, know what to expect.
Permanent infertility on all those vaccinated.
Syncytin-1 is also present on , I find it interesting that the “Fact Check” from the 12/16/20 issue of USA Today referenced that the vaccine had been given without causing infertility–the first dose had been given 12/14/20. The 12/16/20 “Fact Check” was later taken off of their website.
What I find most interesting is that the vaccine is still in very early use. From the Wall Street Journal 12/14/20;
A nurse in New York was among the first to receive the shot Monday morning. Thus far, there have been no documented cases of infertility 2 days after the first dose of the vaccine was administered! I don’t find it terribly reassuring that no cases of infertility have been documented within 48 hours of the initial dose.
This smells of media collusion.
So, we know that the vaccine binds to Syncytin-1, present on human sperm & egg cells, is present on the placenta, participates in the fusion of cells and was integrated into our genome, our DNA from Human Endogenous Retroviruses (HERV’s). Will the same happen with the mRNA of the Covid19 vaccine, that within 48 hours has not caused infertility? Then again, I’ve never heard of anything that causes infertility within 2 days!
Physicians practice medicine. Just as engineering involves “applied physics”, medicine is “applied biology”. I don’t need a newspaper to tell me where antibodies to syncyntin-1 are heading!
The first of it’s kind EVER Messenger RNA (mRNA) Virus
The most likely Covid19 vaccine candidates contain mRNA (messenger RNA), which is a genetic template that instructs our cells to build the viral proteins that our immune systems can then recognize. Its main perk is that allowing our bodies to produce the proteins (rather than growing them in a lab like traditional vaccines) slashes production time. For nearly 20 years, researchers have been interested in using mRNA in vaccines; and some were even tested in early clinical trials for rabies, influenza and Zika. However, the vaccines for COVID-19 will be the first mRNA vaccines ever approved by the FDA.
Covid Morbidity & Mortality
False positive tests, higher reimbursement rates for Covid patients than non-Covid patients, there are numerous reasons why the US data is skewed heavily toward positive tests and thus more cases which in turn affects the rates of morbidity (illness) & mortality (death). Our data input has inaccuracies that can skew all further interpretations and projections.
Clearly, any data on incidence rates of Covid19 would be nonsense. Hospitals and doctors would be inflating the rates of Covid19 before we even had test kits!
Remember, we did not have Covid testing available in February of 2020! Those test kits wouldn’t arrive until after April 2020 and would have numerous problems;
- Contaminated tests (some of which were contaminated WITH Covid guaranteeing a positive test!)
- Early warning signs on flawed testing ignored
- Limited testing slow roll-out
- Complicated process and paperwork
- Denial and dysfunction at the highest levels of government
When testing began in earnest many people were found to have antibodies to Covid19, people who couldn’t recall having the illness.
This means that Covid19 can present as a “silent” (asymptomatic) disease; you can have the disease, not know it and develop antibodies to it.
I don’t mean to say that there’s no such thing as Covid19, obviously, there is.
I will say that the incidence rate of the disease and the death rate are MUCH lower than we’ve been lead to believe. The observed number of deaths represents only a minority of all infections.
Studies show that at least 40-to-50% of people who test positive for COVID-19 have no symptoms. Medical experts initially said asymptomatic spread clearly is contributing to spikes of COVID-19, later this claim was retracted.
To calculate morbidity (illness) & mortality (death rate) of an illness, the entire number of people afflicted needs to be taken into consideration. Think of an iceberg. The tip of the iceberg is all we see, but we know that the majority of that iceberg is underwater.
To calculate true morbidity & mortality, we need to look at ALL PEOPLE WITH A HISTORY OF EXPOSURE. This includes an unknown but huge amount of folks who never had symptoms but developed antibodies (the iceberg we cannot see underwater).
Numerator = Number of Deaths/Denominator = Total Number of Cases
We know that the numbers have been exaggerated from the HHS letter of February 2020 to all practitioners, that’s the exaggerated numerator, the denominator includes them AND EVERYBODY WHO HAS EVER DEVELOPED NATURAL ANTIBODIES TO THE VIRUS (without the vaccine), thus meaning they were exposed even if asymptomatic. This drives the illness and death rate much lower than we’ve been lead to believe.
If these cases are taken into the equation of determining morbidity (illness) & mortality (death) rates of the disease, the numbers drop dramatically.
Again, garbage in, garbage out for US data, we need to look at the experience of other countries for any hope of getting accurate data–and even then, we don’t know if other countries have had the same problems as the US has had regarding Covid19.
Pandemic Treatment Principles:
When any epidemic or pandemic arises, early in the course, morbidity (illness) & mortality (death) rates are highest early in the disease before effective treatments are discovered.
Covid19 is no exception.
We now have very effective treatments, death rates are declining from what they were early on. Even if cases increase, with adequate therapy recovery will happen. Folks with advanced age or other comorbidities (other illnesses that take a toll on their metabolism/homeostasis) are still going to have higher death rates, reasonable precautions should be used. The graphs above indicate a high number of cases in middle-age, fewer cases in the elderly but with a higher death rate than occurs in middle-age despite the increase in cases–as should be expected later in an epidemic or pandemic.
The demographics above provide insight into age & ethnicity, and the associated case rate vs. death rate.
From the US Dept. of Defense, since the completion of the Human Genome Project in April 2013 we now know what genes control what ethnic characteristics, enabling a savvy genetic engineer the ability to target an epidemic to any given characteristic such as ethnicity or other variable.
A nuclear weapons program can be monitored remotely via radiation, will be large and require a great deal of infrastructure and support.
A bioweapons research lab can be set up in any university or medical setting, thus operating “underground” in a clandestine setting, impossible to detect and/or monitor. We had mapped out the gene sequences on at least 599 viruses, 205 naturally occurring plasmids, 31 bacteria, 1 fungus, 2 animals, and 1 plant as of February 2001–much more has been accomplished in the last 2 decades!
Binary biological weapons:
This bioweapon is made up of a two-component system with independent elements that are safe to handle separately but when mixed together form a lethal combination. This system consists of a virus and helper virus, or bacterial virulence plasmid. Hepatitis D is an example of a virus and B as the helper virus; a combination of both produces severe infection to the host.
Viruses can be used to cause illness in epidemics–but also more insidiously to cause cancer at a later date. Use of binary biologic weapons would be difficult if not impossible to detect–at some point, perhaps decades or years later a given population could have an “epidemic of cancer”.
From April 12, 2009 until April 10, 2010, the CDC estimates that up to 60.8 million people were infected with swine flu. That flu led to an estimated 274,304 hospitalizations, and, according to estimates, 12,469 deaths over the course of that year.
This gives a mortality rate of 0.002%
That death count is in huge contrast to the current coronavirus pandemic. Infections of COVID-19 in the US are still increasing, but the latest data from the Johns Hopkins University Coronavirus Resource Center shows that 7.5 million people in the U.S. have been infected with the virus to date. More than 212,000 Americans have currently died of COVID-19, Johns Hopkins reports.
The death rate from Covid19 is highly inflated as noted above, as is the mortality rate.
With the numbers above, the mortality rate would be 2.8%–but we also know that the total number infected (denominator) is MUCH higher and that the death rate (numerator) is MUCH lower. If this were taken into account, if we had accurate data, the mortality rate would plummet.
Garbage In–>Garbage Out
New Approaches to Covid19 Treatment
Early reports from Wuhan indicated that studies have shown that various high-dose intravenous vitamin C infusions (e.g., 200 mg/kg body weight/day, divided into 4 doses) shortened the intensive care unit (ICU) stay by 7.8 % , and was accompanied by a signiﬁcant reduction in the mortality rate in the treatment of severe sepsis and septic shock .
Moreover, vitamin C has also demonstrated antiviral activity which was recently reviewed . Coronaviruses increase oxidative stress that promotes cellular malfunction and ultimately results in organ failure . It is believed that high intravenous dose of vitamin C could be particularly effective by inhibiting the production of cytokines storm due to COVID-19 and many physicians in China have identiﬁed promising results using this approach against COVID-19 [231,232].
- High doses of Vitamin C are notable for having;
- Anti-inflammatory effects. Excess inflammation is one of the biggest problems with Covid19
- Anti-histaminic effects
- Anti-oxidant effects
- Numerous other beneficial effects useful in treating Covid19
Vitamin C works best when given with adequate amounts of zinc sulfate 220 mg (50 mg of elemental zinc) twice daily. Despite all of this, high-dose vitamin C is rarely used in hospitals to treat illnesses.
The next drug used was hydroxychloroquine–then on March 24, 2020 NC pharmacists were told by the NC Board of Pharmacy that they could not dispense the drug unless the patient had a diagnosis of rheumatoid arthritis, or only a 14 day supply of the medicine could be dispensed to patients with documented Covid19 (a positive test). 200 mg twice/d for 2 weeks has been proven effective.
10/9/2020 the National Institute of Health recommend against use of Chloroquine or Hydroxychloroquine to treat or prevent Covid19 despite the facts that;
- Both chloroquine and hydroxychloroquine increase the endosomal pH, inhibiting fusion of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and the host cell membranes.1
- Chloroquine inhibits glycosylation of the cellular angiotensin-converting enzyme 2 receptor, which may interfere with binding of severe acute respiratory syndrome-associated coronavirus (SARS-CoV) to the cell receptor.2
- In vitro studies have suggested that both chloroquine and hydroxychloroquine may block the transport of SARS-CoV-2 from early endosomes to endolysosomes, possibly preventing the release of the viral genome.3
- Both chloroquine and hydroxychloroquine also have immunomodulatory effects.
I have not seen any widely published studies attesting to the lack of effect of these drugs–many people have used it & had a speedy recovery.
I’ve seen patients improve and recover with Covid19–why is this drug that has established a track record being passed off as ineffective?
Granted, the medicine can cause cardiac effects–but has been used to treat malaria and arthritis for decades!
Ivermectin is an inexpensive, commonly used, safe anti-parasitic drug used to kill parasites including onchocerciasis, a worm that causes river blindness among other diseases, scabies, lice, among others.
As it turns out, it’s also very effective against Covid19.
Budesonide is a synthetic steroid of the glucocorticoid family with a high topical anti-inflammatory activity that helps reduce the cytokine storm in the lungs, it’s marketed in the US as Symbicort.
It can also be nebulized/inhaled to treat the cytokine storm in the lungs common in Covid19.
Blood clotting problems “thrombosis” is also common in Covid19, yet typically responds well to traditional treatment.
Concerns Regarding the Covid19 Vaccine:
So… We have numerous effective treatments for Covid19, despite this, we’re being pressed to hurry up and get this vaccine. A vaccine using never-before-used messenger RNA (mRNA), released with inadequate testing for safety for this pandemic that has numerous effective treatments, many of which are quite inexpensive.
A vaccine would make sense if there was no effective therapy–but there IS good treatment for this infection.
This sounds dangerous to me with minimal studies regarding it’s safety and any long-term effects.
Is it possible that the mRNA could be incorporated into our DNA? We don’t know… Human Endogenous RetroVirus could lead to the incorporation of this foreign messenger RNA into our genome, altering it forever, into perpetuity. We don’t know how many HERV’s there are or how prevalent they are in the population.
What if… RNA dependent DNA polymerase (such as that from a HERV) made it into the system or the virus mutated to acquire it–then our genomes would be forever altered–is this something we want, for our DNA and that of our bloodline to be changed forever by a manmade virus. Could this sterilize the human race?
We don’t know.
Will mRNA generate antibodies against itself, negating it’s effect?
Will it elicit the complement cascade?
Our gut was designed to allow single amino acids and single sugars from starches to enter the blood stream. Proteins and polypeptides (smaller amino acid chains than a protein), complex carbohydrates which are chains of various sugars bonded together, can all generate antibody response, immune complex formation and complement activation. Single units (called monomers) tend to not produce an immune reaction, multiple units (called polymers) are more likely to generate an immune reaction.
About 25% of the human population has a genetic anomaly in which there is faulty macrophage presentation of antigen to the T-Cells–essentially it’s an immune system with a “broken off-switch” which ultimately generates a pro-inflammatory cytokine storm leading to chronic inflammation and autoimmunity
Recall that this vaccine is the first of it’s kind ever mRNA vaccine. The only conclusion that can be drawn from this is that the mRNA vaccine contains retroviral components. HIV is a retrovirus, a retrovirus uses the reverse transcriptase to incorporate itself into the host (human) genome. This is evidence that the vaccine mRNA will be permanently placed into the human recipients genome, altering it forever.
CRISPR (clustered regularly interspaced short palindromic repeats). This technology essentially allows for the editing of genes to change what they do and what type of proteins or genetic regulatory centers that turn genes on and off. Genes can be customized to do what we want, it would be relatively easy to generate genetic code for RNA-dependent DNA Polymerase to insert unwanted genetic code into our genomes
Epigenetics involves the effects on cellular and physiological phenotypic traits may result from external or environmental factors, or be part of normal development. The standard definition of epigenetics requires these alterations to be heritable in the progeny of either cells or organisms.
The following is factual information about existing technologies–I have no evidence that it is being used or ever will be used in these vaccines.
Researchers headed by a team at the Massachusetts Institute of Technology (MIT) have created a microneedle platform using fluorescent microparticles called quantum dots (QD), which can deliver vaccines and at the same time invisibly encode vaccination history directly in the skin. The quantum dots are composed of nanocrystals, which emit near-infrared (NIR) light that can be detected by a specially equipped smartphone. Tests using the platform showed that QDs delivered to samples of human skin were still detectable after photobleaching that simulated five years of exposure sunlight, and they remained detectable for up to nine months when tested in rats.
Vaccine administration methods have included talk of the use of a microdot hydrogel delivery system.
What other things could be delivered to unknowing recipients with this system?
We know that “big brother is listening/watching.
Who else is monitoring us? These implications could be devastating. We can leave our phones at home, but there may be things we don’t count on that will be with us always…
I believe we all recognize that our cell phones will interrupt us with comments, we get targeted advertising based on conversations we’ve had but notably have not done a search on any given product; Big Brother (Google?) is clearly listening and likely watching.
At least we can walk away from our tech devices–do we really want God knows what implanted into our very bodies?
This Document Would be Incomplete Without Mention of Other Issues;
China locked down internally for COVID-19, but pushed foreign travel the net result being that China was somewhat spared by this pandemic but the rest of the world was put at higher risk.
So; What Should We Do Regarding this Covid19 Vaccine?
I can think of 3 responses to the Covid19 vaccine offer, interestingly, I think these can also be thought of as the 3 answers to our prayers.
- Yes; I’ll accept the vaccine as it is offered.
- No; I won’t take this vaccine
- Not Yet/maybe later, I need time to see how others who receive it fare.
The choice, ultimately at this time, is yours.
Will that change? As of 12/15/20 entering the search term “Mandatory COVID 19 Vaccine” into Google’s search engine generated About 263,000,000 results.
At this time there are no clear mandates COVID19 vaccination in the US.
We live in the greatest country on earth. The choice is yours, this document is provided to help you choose wisely.