A very interesting write up with background on how bacteria, both good and bad, could be involved in Covid-19, and gene therapy adverse effects. There is also some interesting information on the negative consequences of antibiotic use. And there are a lot of links to delve into further .
https://amidwesterndoctor.substack.com/p/an-important-citizens-investigation
•Because the mRNA was modified to resist degradation in the body (so it could produce sufficient vaccine product), and the manner used to do this (pseudouridation) is quite haphazard, it is very likely that some of the vaccine mRNA persists for months inside the body. The only study that has ever looked at this issue found that mRNA was still present 60 days after vaccination, and did not look beyond that timeframe.
•The mRNA is changing the DNA of cells, and causing them to begin to permanently produce spike proteins. Research has now shown that mRNA alters the DNA of cells, but it is not clear if this change is enough to cause significant and sustained spike protein production throughout the body.
•Some vaccinated individuals (e.g., those who develop myocarditis) cannot form antibodies to the spike protein, and this causes the vaccine spike proteins to persist for a very long time within the body.
•The vaccine eliminates the body’s ability to get rid of a COVID-19 infection, and as a result, a chronic low-grade COVID-19 infection develops, which continually manufactures spike proteins in the body.
Antibiotics are one of the modern-day miracles of medicine, and their ability to save lives has fundamentally improved our modern lifestyle to the degree that most have difficulty even comprehending today. Conversely, since antibiotics were first discovered, practitioners from many different medical systems have noticed that they seem to cause a variety of issues that can outweigh the benefits of the therapy. Most of these issues are encapsulated under the belief that antibiotic therapy trades an acute disease for a chronic one. In general, the issues tend to fall under one of the following:
•Antibiotics are toxic to the batteries of our cells, the mitochondria (mitochondria evolved from bacteria and share many similarities to them).
•Individuals can have allergic reactions to the antibiotic (although this is the most obvious issue, it typically has the most minimal long-term consequences for a patient).
•Antibiotics have a high degree of general toxicity which typically results in them being pulled from the market once safer options are made available (sadly this can often take years).
•Antibiotics pathologically disrupt the gut microbiome (leading to digestive problems) and pathologic bacterial evolution.
Unfortunately, in conventional medical practice, most of these issues are not recognized, and doctors typically focus on determining which drug the bacteria are least likely to have antibiotic resistance towards (as this is what medical training primes you to focus on). This bias frequently results in dangerous and not necessarily needed antibiotics being prescribed, because “allergies” and antibiotic availability are typically the only contraindictions considered. In short, there are a lot of issues that arise from antibiotics being given out like candy.
Since there are so many things that could have gone awry, despite a lot of research on the subject, I genuinely admit I had not even considered this possibility there could be plasmid contamination adversely transforming our entire microbiome. However, as I hope this article has shown, in hindsight, it makes a great deal of sense. All of this should illustrate just how many serious issues can happen when an experimental vaccine is rushed to market and critical steps (such as sufficiently removing the bacterial plasmid from the final product) are skipped—especially with a gene therapy.
As you might guess, these quality control issues were particularly apparent within my “favorite” pharmaceutical company:While the Moderna vaccines are meeting this specification [the maximum allowable plasmid contaminant level originally proposed by regulators], the Pfizer [vaccines] are 10-fold higher in contamination with 1 DNA molecule per 350 mRNAs. This is 1 replication competent plasmid per 350 mRNA molecules and equates to billions of antibiotic resistant plasmids injected per person per shot.