Prior to Covid 19 the vaccine argument was widening to a broader audience and becoming increasingly animated between those for and those against. The timing of the Covid 19 outbreak has deflected the growing general vaccine debate, amongst other more pressing critical issues, such as the endangerment of much of earth’s species of wildlife particularly in the oceans, the melting of the polar ice caps and the deterioration of the ozone layer.
Our society is polarising, with the Covid 19 virus pandemic and its subsequent immunisation program, adding impetus. There are always two choices and two paths, with people now facing the decision whether to receive an inoculation, or not.
Vaccine development can be broadly classified into two categories: gene-based and protein-based. Over past decades, traditional viral vector vaccines place a live, though weakened or inactivated disease germ, such as adenovirus – that causes the common cold – into the body as a shell to carry genetic code to cells, similar to a Trojan Horse. Once the specific genetic instructions are inside the nucleus of the body’s cells, the cells produce a spike protein to influence the body’s immune system and so create antibodies and memory cells to protect against a future infection.
Genetic engineering is an experimental technique, using genes to treat or prevent disease, either by a. replacing a mutated gene causing disease with a healthy copy, b. inactivating a mutated gene that is malfunctioning or c. introducing a new gene to fight a disease. It is in its infancy, with ethical concerns yet to be addressed or regulated and it continues to be controversial. Gene therapy involves inserting a new gene directly into a cell. The challenge, is targeting the new genes to the specific cells required and then also ensuring the new genes are precisely controlled by the body.
The mRNA vaccines fall into this category using a novel technology that has never been approved for widespread use. They do not contain a live virus but a synthetic, lab developed nucleoside-modified version of mRNA – messenger ribonucleic acid – a molecule coated with lipid nanoparticles** that provides the genetic code for reprogramming the body’s cells into making proteins to create antibodies.
The concern with the Covid 19 mRNA vaccines… [similar to retroviruses which contain a RNA genome that creates a DNA copy by reverse transcription, this then integrates into the cell of the host, literally inserting itself into the host cell’s genome; becoming a permanent part of it in the form of a sequence called a provirus. The proviral sequence is then transcribed in the host cell to produce viral proteins and particles that spread to the next cell – the most famous retrovirus being HIV-1^ – actually integrating their genetic material, (along with the new gene) into a chromosome in the human cell]… is that the mRNA vaccines are altering human DNA.
The standard response from officialdom is that these ‘vaccines do not change – or interact with – a recipient’s DNA’ and that ‘mRNA vaccines act entirely within the cytosol [Cytoplasm – see cell diagram] of the cell – they do not go near the nucleus where all the DNA is’ as supported by Alliance for Science:
‘… mRNA… does reprogram some of your cells… And that’s not a defect – it’s intentional… mRNA… is basically… a single-stranded nucleic acid that carries a genetic sequence from the DNA in the cell’s nucleus into the protein factories – called ribosomes [see cell diagram] – that sit outside the nucleus in the cellular cytoplasm… mRNA stays in the cytoplasm, where the ribosomes are. It does not enter the nucleus and cannot interact with your DNA or cause any changes to the genome. You might ask whether this DNA can genetically engineer your cells… the answer is no. DNA is injected in little circular pieces called “plasmids”… and while these do enter the nucleus, the new DNA does not integrate into your cellular genome.’
Web MD also assures us that, ‘for the vaccines to alter a person’s genes… the mRNA instructions would have to enter the cell’s control center, the nucleus. The nucleus is walled off from the rest of the cell by its own membrane. To get past that membrane, the mRNA would have to have an enzyme called a nuclear access signal… “which it doesn’t have.” Even if it could get into the nucleus, the single strand of mRNA would have to be translated back into a double stranded DNA. HIV^, the virus that causes Aids, can do this. It uses an enzyme like reverse transcriptase to insert itself into our chromosomes. The mRNA in the vaccines lacks this enzyme, so it can’t turn back into DNA. The DNA adenovirus used in the Johnson & Johnson vaccine does enter the nucleus of our cells, but it never integrates into our chromosomes.’
The Science Daily contains a report by The Mount Sinai Hospital & Mount Sinai School of Medicine, 2017: ‘Influenza A is responsible in part not only for seasonal flus but also pandemics such as H1N1 and other flus that cross from mammals (such as swine) or birds into humans. Influenza A is an RNA virus, meaning that it reproduces itself inside the nucleus. Most viruses replicate in a cell’s cytoplasm, outside the nucleus. The researchers found that once inside the nucleus, influenza A hijacks the RNA exosome, an essential protein complex that degrades RNA as a way to regulate gene expression.
The flu pathogen needs extra RNA to start the replication process so it steals these molecules from the hijacked exosome, Dr. Marazzi says. “Viruses have a very intelligent way of not messing too much with our own biology… It makes use of our by-products, so rather than allowing the exosome to chew up and degrade excess RNA, it tags the exosome and steals the RNA it needs before it is destroyed.”
“Without an RNA exosome, a virus cannot grow, so the agreement between the virus and host is that it is ok for the virus to use some of the host RNA because the host has other ways to suppress the virus that is replicated,” says the study’s lead author, Alex Rialdi, MPH, a graduate assistant in Dr. Marazzi’s laboratory.’
Thus we learn that the nucleus of a human cell is vulnerable to attack and therefore, it is not unrealistic to be concerned with the possibility of an unwanted intrusion stemming from a Covid 19 ‘vaccine’ side effect. And though Covid 19 derives from a different virus than that of Influenza and the flu, it behaves in a similar fashion and is unlike say, a measles virus, which can be controlled because it is exclusively in humans and does not mutate. Covid 19 as a coronavirus is intrinsically different; they jump from animals to humans and mutate to evade immunity, which makes it next to impossible to eradicate a virus like Covid 19. It is an endemic virus and ‘something we will have to learn to live with’ like a seasonal flu.
The inventor of the messenger RNA vaccine platform, Dr Robert Malone – who has been vaccinated himself – is expressing concerns on the safety of a mass scale roll out and the unethical ways the Covid 19 vaccine is being promoted – with ‘core bioethical principles… being violated.’ He is surely qualified on both the benefits and the risks of this technology. Dr Malone is calling for a stop to Covid 19 vaccines; explaining that the vaccine can cause an enhanced immune response, with a worse reaction when exposed to the natural coronavirus. It can also create further autoimmunities in the the body. Malone added that the spike protein is the most dangerous aspect, which can open up the blood brain barrier [BBB]. Leading too dangerous implications for the body [fatal blood clots] and explains why there have been adverse reactions to the Covid 19 vaccine.
Pascal Davies elaborates on Euronews, 2021: ‘Rare fatal blood clots linked to the COVID-19 vaccines AstraZeneca and Johnson & Johnson have caused major concerns, but a group of scientists in Germany claims they have cracked the code as to why this is happening. The researchers suggest vaccines that put adenovirus vectors – the cold viruses used to insert the spike protein of COVID-19 into the nucleus of the cell – into the body can, in some people, cause bits of coronavirus proteins to enter the nucleus and break up. The fragments then exit into the bloodstream and can cause clotting. The rare clumps in the blood can then become serious if the clots approach vital organs. The scientists wrote in a pre-print study… that the vaccine is delivered to the nucleus of the cell rather than to the fluid around it that acts as a protein factory. “The adenovirus life cycle includes the infection of cells… [and] entry of the adenoviral DNA into the nucleus, and subsequently gene transcription by the host transcription machinery… And exactly here lies the problem: the viral piece of DNA… is not optimised to be transcribed inside of the nucleus”.’
The mRNA in the Covid 19 injection is coated with lipid nanoparticles and the standard official medical argument is that these are very unlikely to enter the brain, though it is conceded that it is a possibility of which it is then admitted, that the repercussions of such an eventuality are unknown. But, we are then reassured that any side effects are outweighed by the possible dangers of Covid 19 complications.
Shin Jie Yong addresses this matter on Microbial Instincts, 2021: ‘Jacob Wes Ulm, MD, Ph.D., a geneticist, explained this concern in detail in a letter to the British Medical Journal, as well as in a public comment to an article about mRNA vaccines on January 2021: “…it seems that they (mRNA vaccines) can enter a much broader tissue range compared to even attenuated virus vaccines… And since the mRNA vaccines would induce SARS-CoV-2 viral spike protein expression, that seems to mean that people who get the mRNA vaccines are going to have a much greater range of cells and tissues vulnerable to cytotoxic (T-cell) attack… with side effects that may not manifest for years (with cumulative damage and chronic inflammation).
This is where the picture gets aggravatingly murky,” Dr. Ulm added, mentioning that there seems to be no comprehensive data on the cellular localization – i.e., which types of cells the biomaterial enters – of the LNPs used by Pfizer-BioNTech and Moderna. Although there have been past studies on the cellular localization of LNPs, different LNP formulations would enter different cell types, Dr. Ulm stated, so “we don’t know where in the body they’re going,” adding that: “The nightmare scenario would be if [for example] the mRNA vaccines’ lipid nanoparticles are, indeed, crossing the BBB and getting endocytosed into critical glial cells, like oligodendrocytes, or even worse, into neurons themselves in the brain and spinal cord, putting a bullseye on these critical cells for cytotoxic (T-cells).”
‘European Medicines Agency’s (EMA) assessment report of the Moderna mRNA vaccine has reported: “Low levels of mRNA could be detected in all examined tissues except the kidney (in rats). This included heart, lung, testis, and also brain tissues, indicating that the mRNA/LNP platform crossed the blood/brain barrier, although to very low levels (2–4% of the plasma level).” Therefore, these reports suggest that the LNPs can carry bits of the mRNA vaccine into the brain. But we still don’t know what would happen after the mRNA vaccine enters the brain.’
Dr Malone apparently supports the premise offered by some, that the Covid 19 ‘shots are not vaccines but gene modifying interventions.’ According to Malone: “The German government has specifically outlawed the use of gene therapy-based vaccine as a term.” In response to his concerns, his personal Wikipedia page has been cut and all references to Robert Malone inventing the mRNA technology have been removed and attributed to various institutions. Malone likens these actions to George Orwell’s 1984; ironically, an official denial of vaccine dangers has been Federal Policy in the United States since 1984.
Evidence of this, is that vaccine companies perform their own safety and efficacy testing, over very short periods of time [days], using questionable controls, then declaring their products safe and effective; all without independent and valid testing. Plus, vaccines are not tested for their carcinogenic, mutagenic or impairment of fertility effects, despite containing cancer causing ingredients that can alter or damage DNA, RNA, fertility and sterility. Particularly as with even general vaccines, they are permitted by government regulators to contain ingredients that do not have to be listed [such as: ‘toxic chemicals, unidentifiable protein aggregates, nanoparticles, and nano-contaminants not listed as ingredients on package inserts].’ Those who administer vaccines and those who receive them, are not truly informed as to the full contents of the injection.
Vaccines contain ingredients that are either not required by the human body, are dangerous to the human body [especially when injected] or for ethical, religious reasons are unacceptable. For instance those who are Vegans, eat a plant-based diet, are Islamic or Jewish. Vaccines are tested on animals. Ingredients can include a cocktail of: ‘aluminum [Aluminium], mercury, formaldehyde, polysorbate 80, antibiotics, viruses and retroviruses of both human and animal origin, aborted human fetal material, DNA, RNA’ and hormones ‘of both human and animal origin’ [from urine, including: pigs, rats, mice, primates, cattle, sheep, horses and guinea pigs], ‘phenol, stainless steel, tungsten, lead, squalene, endotoxins, glyphosate, sodium borate, food proteins, Triton-X detergent, gelatin, egg proteins, yeast, glass shards, and blood-poisoning bacteria.’
The implications of the Covid 19 injection are worthy of investigation. In coming years, we may well experience a wave of viral mutations and variants in an ongoing pandemic crisis, all the while enduring successive booster vaccinations; with ever more strict legislation, restrictions and loss of freedoms.
The paradox is that with abortion rights – there is the freedom in the terminating of a life – it is my body, my choice. Yet society is being coerced by governments, today – possibly forced tomorrow – to imbibe a preparation into their system; in complete contradiction to ‘my body, my choice.’ It behooves us all to question what are the facts, which is the misinformation and arrive at an informed verdict, the best decision… the right choice.
What is an injection today, may become a pill tomorrow. In a dark reflection of life imitating art, our world is merging with the one portrayed in the 1932 novel, Brave New World by Aldous Huxley. Whereby pharmaceutical drugs, propaganda fuelled world news and a hypnotic social media controls everyones life in conformity. Add to this total subordination and equality of all citizenry, achieved through the restraint of our personal wealth via a worldwide centralised digital currency revolution.
‘[Research] shows that SARS-CoV-2 mRNA can integrate into human DNA. Using the Reverse Transcriptase (RT) found in human platelets, CD4 (Helper Cells) and other cells carrying Long Interspersed Nuclear Elements (LINE-1); or by the HIV-RT. LINE-1 averages 6,000 base pairs (bp) and comprises approximately 17% of human DNA… 80-100 of these LINE-1 segments are known to retro transpose leading to insertions, deletions, and rearrangement of genetic material.’
Image below shows mRNA inserting itself into brain cells
‘Evidence shows that the virus is engineered with Gain of Function (GOF) [a controversial medical research practice that involves genetically altering a virus or pathogen to ‘enhance the biological functions of gene products’ – in other words: it primarily ‘refers to viruses being taken from animals before they are genetically altered in a lab to make them more transmissible to humans‘] including mechanisms creating an Inflammo Thrombotic Response (ITR)… with Prion-like structures in the virus spike protein. Prion-like domains are critical to SARS-CoV-2 virulence. Prions are associated with “Mad Cow Disease” and neuromuscular movement disorders seen in Parkinson’s Disease and Alzheimer’s’ including ‘Creutzfeldt–Jakob disease (CJD)… a fatal degenerative brain disorder.’
The UK government has revealed that once you have been double-vaccinated, one will never be able to acquire a full natural immunity to Covid variants; or possibly, any other viruses. The UK Department of Health stated on page twenty-three of its most recent Covid-19 Vaccine Surveillance Report Week 42: “N antibody levels appear to be lower in people who become infected after two doses of vaccination.”
This drop in antibodies is permanent. Covid-19 vaccines do not prevent infection or transmission of the virus. The report states that vaccinated adults are more likely to be infected than unvaccinated people. As the vaccine ‘interferes with the body’s ability to make antibodies after infection not only against the spike protein but also against other parts of the virus.’
Vaccinated people seem to lack the ability to form antibodies against the nucleocapsid protein – the envelope of the virus – a vital part of the response in unvaccinated people. Thus the vaccinated are considerably more ‘susceptible to any mutations in the spike protein, even if they have already been infected and cured once or more.’ Compared to the unvaccinated, who gain lasting immunity to all strains of the virus after being naturally infected, even just once.