Covid

The COVID-19 pandemic caused much illness, many deaths, and profound disruption to society. The production of ‘safe and effective’ vaccines was a key public health target. Sadly, unprecedented high rates of adverse events have overshadowed the benefits. This two-part narrative review presents evidence for the widespread harms of novel product COVID-19 mRNA and adenovectorDNA vaccines and is novel in attempting to provide a thorough overview of harms arising from the new technology in vaccines that relied on human cells producing a foreign antigen that has evidence of pathogenicity. This first paper explores peer-reviewed data counter to the ‘safe and effective’ narrative attached to these new technologies. Spike protein pathogenicity, termed ‘spikeopathy’, whether from the SARS-CoV-2 virus or produced by vaccine gene codes, akin to a ‘synthetic virus’, is increasingly understood in terms of molecular biology and pathophysiology. Pharmacokinetic transfection through body tissues distant from the injection site by lipid-nanoparticles or viral-vector carriers means that ‘spikeopathy’ can affect many organs. The inflammatory properties of the nanoparticles used to ferry mRNA; N1-methylpseudouridine employed to prolong synthetic mRNA function; the widespread biodistribution of the mRNA and DNA codes and translated spike proteins, and autoimmunity via human production of foreign proteins, contribute to harmful effects. This paper reviews autoimmune, cardiovascular, neurological, potential oncological effects, and autopsy evidence for spikeopathy. With many gene-based therapeutic technologies planned, a re-evaluation is necessary and timely...

There are significant implications of this study.

The BNT vaccination did induce anti- spike and anti-Receptor Binding Domain ( anti RBD) Ig G antibodies, demonstrated in this study at 1 month and persisting to 6 months post vaccination, indicating a Th2 immune system 'humoral' and ' adaptive' response, together with increased cytokine responses on exposure to spike protein or the whole Covid virus tested. This should equate to enhanced immunity against Covid and the spike protein if normal mucosal immunity is maintained.

However this study also clearly demonstrated that the cytokines (or cell messenger molecules) required for the initial response of the innate, cell-mediated immunity prior to antibody formation, to numerous tested viruses and bacteria, were dramatically decreased after 1 month. Interferon gamma, the key messenger to activate the first arm of the immune system which lives in the mucosal tissues lining our airways and gut, was reduced some tenfold, as was 

MCP-1, a protein which attracts monocytes into tissues, another key player in innate cellular immunity. The immune system, simplified, has 2 arms: innate and adaptive. The innate immune system lines the mucosal barriers of the respiratory and gut particularly, is the first and major barrier to any and all infections and is predominantly mediated by immune cell actions. This is also called TH1 immunity.It is only after an infectious agent has traversed the mucosal barrier that specific antibodies – the adaptive immunity – are made. This is often called TH2 immunity. This study made it very apparent that while the Covid vaccine induces anti spike antibodies, it markedly reduces initial protective responses to many other viral and bacterial infections as measured at 1 month post vaccination, with persistent reductions in antiviral protection to 6 months. A similar effect has also recently been shown in adults. This same mechanism of action likely occurs with all other injectable vaccinations.

The bigger question of how this is altering overall immune function is gradually being acknowledged: 'Our results add to the evolving evidence that SARS-CoV-2 mRNA vaccination reprograms both adaptive and innate immune responses.' Our immune systems are being 'reprogrammed', like a faulty computer programme needing to be rewritten or upgraded. Although not acknowledged in the abstract conclusion, the authors state that ' Our findings suggest SARS-CoV-2 mRNA vaccination could alter the immune response to other pathogens, which cause both vaccine-preventable and non-vaccine-preventable diseases . This is particularly relevant in children', and 'That SARS-CoV-2 mRNA vaccination in children could impact immune responses to other pathogens emphasises the need for further research and consideration of heterologous effects in vaccination policies given their broad public health implications.' They acknowledge there is a potential issue here. Perhaps this is behind the surge in Streptococcal infections in children being noted worldwide?

For our children to be healthy, they need a well -functioning innate immune system lining the gut and respiratory mucosa, first and foremost. This does not need reprogramming but support. This does not come by vaccination.

residual ongoing symptoms, or as a result of Covid vaccinations which were forced onto unsuspecting and

trusting populations.

It is now very clear that the spike protein itself is highly pathogenic (disease causing) and it seems that

failure to clear the spike protein and the inflammatory and other immune effects it creates underlies both

long covid and vaccine side effects. Long Covid appears to be akin to Chronic Fatigue Syndrome, with

many symptoms and biochemical markers essentially the same, indicating mitochondrial damage in

addition to the other effects. As the vaccines contain not only altered mRNA coated in synthetic charged

lipids to stimulate ongoing spike production in our cells, but are also 'contaminated 'with DNA plasmids,

lipopolysaccharide endotoxin from the bacteria E coli used in manufacture, metals and other unknown

substances, the side effects of these are still being uncovered.

Fortunately there are things that can be done. A paper soon to be published details many of the possible

nonpharmaceutical interventions but a simple effective treatment protocol can be put together yourself

from some the products available on this site.

My suggestions would be: