Parasite Lost

Well, it seems the mRNA experimental jabs are indeed capable of being reverse transcribed into DNA and incorporated into the human genome. I didn’t think it likely, but the experiments have been done and there it is.

Okay, well, it’s actually not new. Many viruses have done this in the past (the most famous example being HIV, of course) and it’s a logical step on the way to becoming the perfect parasite.

A virus is just a bit of DNA or RNA and has only one purpose. To reproduce. However, it has no metabolism so it can’t do that on its own. It has to parasitise another cell – and in doing that, it often kills or debilitates the cell. This means that other cells develop resistance to the entry of that virus (maybe by changing surface receptors or by having, in larger species, an immune system to deal with it). Yes, it’s much more complex than that but that’s the basics.

The ideal outcome for one of these little bits of DNA/RNA is to get incorporated into a higher cell’s DNA permanently. Then it has no further need to express its genes, no need to cause any issues at all, and it’ll be copied when the host cell reproduces. It need do nothing else.

HIV has not reached that stage. Neither has chicken pox, nor any of the others that later reappear and cause sickness. Many have though, and you never hear about them because they don’t do a damn thing. They are part of that ‘junk DNA’ you hear about – parts of the human genome that don’t code for anything or ever express any activity. They just sit there waiting for the cell to reproduce, and they get copied along with it.

Perfect parasites. The host does all the work and they do nothing at all. Ever. They never cause any harm, they just ride along like Burberry-clad genes, soaking up benefits and donating nothing in return.

Some have not reached the perfect parasite stage. They can come back later to make the host’s life miserable and then they will have to take the consequences – the host will do anything it can to get rid of them. Burberry-clad genes who were quiet for a while but then got at a few cans of Red Stripe and kicked off, if you like.

Many viruses will never get to the perfect parasite stage. Ebola is far too nasty and kills far too quickly. It has never shown any sign of developing a less lethal version of itself so it’ll never produce an infection of low enough lethality to have time to get into the host genome. Rabies tries, it can lie dormant for a long time after a bite but it always gets you in the end. It can’t get to perfect parasite level.

So, if this mRNA jab can incorporate into the host genome, will it get to perfect parasite stage and just be another bit of benign junk DNA? Unfortunately I don’t think so.

This virus is clearly engineered. It’s not natural so we can’t assume it will follow any natural rules. It has emerged that Moderna had a patent on a sequence in this virus three years ago. I have limited experience with patenting biological discoveries and one thing is for sure, it’s not a fast process. If they got the patent three years ago they had the sequence at least five years ago.

At this point it’s worth making clear that the experiments I’m referring to concerning covid have all been done in vitro. They used human liver cells but they have not tested this effect in animals and certainly not in humans. Their results must be considered with that caveat. In Vitro human cell lines aren’t always an ideal model – they are close but not a perfect match for what something will do in the entire organism. At this stage all we can say is that it’s possible that it could happen in humans but it’s not certain that it will.

Anyway. This engineered mRNA codes for a spike protein that doesn’t actually perfectly match any known coronavirus. The hope seems to have been that it would induce a generic response to spike proteins but again, that has not been adequately tested. There has also been no study into its potential incorporation into host genome before the jab rollout and therefore no study into whether it would keep producing spike protein from within the host DNA if it was incorporated.

Basically, nobody really knows. It’s all still experimental.

I had an advantage, you can call it an unfair advantage if you like but it took me a lifetime of study to get it. I knew from the outset the limitations of PCR and lateral flow tests. I knew what mRNA producing spike proteins could do to the cells in the human body. I knew about the cruciform plate and the dangers of poorly trained people ramming swabs up there. So I have never taken any type of covid test and have never accepted the jabs. I did try to tell others, but it seems they prefer to scoff. Well, I tried.

I did not know about aspiration – pulling back on the syringe before injection to make sure the needle is not in a blood vessel. I’ve never injected anything into anyone. Seems many of those injecting this stuff didn’t know either.

I was sure mRNA could not be reverse transcribed into DNA in a human cell. I was wrong, that has now been demonstrated to be possible. It has also been shown to be possible that it could be incorporated into the host DNA. Not absolutely proven (it has only been demonstrated in vitro) but ‘shown to be possible’ which is quite a concern in itself.

The important next step is to find out what that incorporated DNA does. If it does nothing, if it joins the ranks of junk DNA, well that’s okay. For now. There is still the chance of future reactivation but we won’t know about that for many years.

If it turns cells into permanent spike protein factories then that is an immediately serious problem.

So now I’m waiting for the next stage in this experiment. And I won’t be a lab rat in it while it’s going on.