Covid-19 Vaccines: Informed Consent? | Cassandra Voices

Covid-19 Vaccines: Informed Consent?

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What if I told you that I had a new product – never before used on a population-wide basis – and after coming into use the manufacturer requested that a court compel the authorities to lock away the results of the initial trials from prying eyes for seventy five years?

This same product is made using E.coli bacteria. Yes, they are the little buggers that can give you the runs, but they are not all bad. These same clever E.coli make strands of genetic material or recipes for a protein that’s actually found on the outside of the virus, Sars-CoV2,a beta-corona virus that in healthy people may give them a bad cold. For others it can prove nasty, but in this unfortunate group of people almost anything can prove nasty. This is the same spike protein that is thought to provoke the worst excesses of the immune response when one encounters a beta-corona virus.

The genetic material uses a unique substance N1-methyl pseudouridine, a synthetic base not found in nature as one of the letters spelling out the recipe for spike protein production. This substance, we are told, stabilises the recipe and helps the cell produce spike protein for longer. That can be a good thing because we want spike protein, to allow our immune system to react to it and produce protective antibodies for future use.

That would be all very well if that’s all it did. Pseudouridine, however, produces a phenomena called frameshifting so that the reading of the recipe can go a bit off track. It’s a bit like reading ‘add  4 cups of flower’ and instead adding ‘flour’ to your scone mix. Who knows what you might end up with. Actually nobody knows for sure.

And that’s not the only problem with letting E.coli make products for humans. E.coli have their own agendas. They are living creatures and not machines. They are under evolutionary pressure to disseminate their genes. One of the ways in which they do so is by packaging them into a little envelope called a plasmid and ejecting it out into the world. This is the process used to make the mRNA for the Covid vaccines, only the bacteria don’t just follow the recipe. They are artists and so embellish and improvise and sneak their DNA into the end product.

Now the manufacturer assures us that they are one step ahead of these fiendish creatures and have managed to remove most, but not all of this foreign material. The manufacturers have in the past few years caught a break from the regulators who once upon a time said that the DNA from bacteria had to be so low that it was measured in picograms. It’s now measured in nanograms, which is one thousand times greater!

They reassure us that this tiny amount – albeit one thousand times greater than was previously permitted – is broken down by the immune system. The immune system doesn’t like ‘naked DNA,’ i.e. DNA free-floating in the body. What if it’s not naked, but contained within the lipid nanoparticle, and it enters the cell with the rest of its encapsulated material?

If the DNA passed on to us humans from our E.coli cousins were to confer the ability to photosynthesise, I’d gladly accept the reduction in my food bill, but what does the bacterial DNA code for?

But its ok, or at least the manufacturers tell us it is. The level of DNA set by the FDA is what the manufacturer says is in their products. They’ve tested them and the various regulatory bodies believe them. Fingers crossed behind the back etc etc.

Several independent researchers, however, noticed the crossing of fingers trick and had a look for themselves and found a lot more bacterial DNA. Now who do we believe?

If that isn’t bad enough something else in the vials, and I don’t understand why it is there. This wasn’t presented to the FDA in the original application for licensing as ‘it was considered to be a non-functional part of the plasmid.’ Its presence has been disputed by some regulatory bodies and researchers, but is now actually recorded in the manufacturer’s literature.

This substance is Simian virus 40, not all of the virus, just a portion called a promoter/enhancer sequence. In another incarnation this same substance – genetic material from a monkey virus – facilitates the entry of genetic material into the nucleus and hence the genome of the individual treated. This is the desired aim in this other incarnation, but is it the desired aim in the Covid vaccines? If not then why is it there?

Authorities have sought to reassure those asking questions about SV40 that it is a ‘naturally occurring virus’. Somehow telling me that I am to be injected with a portion of genetic material from a virus that infects monkeys doesn’t reassure me.

Let us speculate for a moment on the ramifications if this genetic sequence did facilitate the entry of the vaccine genetic material into our genetic material. If it was a heart cell or a liver cell nothing might happen. That genetic material may never again be expressed in the lifetime of that individual especially if they were elderly, wherein cellular activity, like most other activities, is slowed right down. If, however, the genetic material is incorporated into a sperm cell, what then? It could theoretically be transferred to the next generation through a baby with rapidly growing cells. What then?

Pseudouridine is a synthetic substance not found in nature. Will we have then created semi-synthetic life forms or trans-humans? And just to stretch this concept to the point of being almost ridiculous, who owns the genetic material? Does the manufacturer have any proprietorial rights over the trans-human creature? When I discussed this with ChatGPT it gave me a long winded explanation as to why this is a complex medicolegal area, but it didn’t say ‘no’.

Maybe I’m over-reacting. Maybe N1-methyl pseudouridine, bacterial plasmid DNA and fragments of SV40 will do me no harm. But what about the lipid nanoparticle?

Surely a fatty bubble couldn’t do us harm, or could it?

Once again, regulatory authorities dispute that there is substantial risk to us humans. They deny the amount of DNA, whether the DNA can incorporate into our genome, whether the mRNA can incorporate into our genome, significance of the SV40 fragment and the potential side effects of synthetic lipids.

The title of this essay is ‘Informed Consent.’ At the time that these products where given emergency use authorisation they were still technically experimental and given the abundance of unanswered questions I would say they remain experimental.

The 1947 Nuremberg Code, formulated after the trials of the Nazi doctors stresses the concept of informed consent before an experimental medical procedure is carried out on a human being. What percentage of the 70% of the world’s population who received these products can say that they gave ‘informed consent’?

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About Author

Dr Billy Ralph is a family physician based at The Ballagh Health Centre, Enniscorthy, County Wexford.

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