Add to this the mRNA integrity issues, wherein the mRNA that is actually delivered in the NLP bubbles is not 100% accurate code for the spike protein. Some percentage is allowed by regulators to be imperfect, and code for unknown goo. According to the 2021 EUA email leaks from Europe, that percentage was on the order of 20-50% (!!!!!!).
Agree. From memory, in either Supply Contracts and/or reg public docs, active ingredient integrity minima were around 55%, begging many unanswered but highly obvious questions.
From memory, the EMA raised concerns about the level of viable mRNA in samples provided by PfizerL in support of its application for emergency approval. The solution? The threshold was lowered and the vaccine received emergency authorisation. Got that?
So essentially, given that we were already under a global antibiotic resistance emergency, to the point that the WHO's ARC advisory working group have determined a whole host of antimicrobials (particularly antibiotics) to be limited to the public, and held in emergency use only format, they have allowed the inhumane injection of multitudes with leaky, contaminated products, that not only migrate to the highly mitochondrial dense areas, but potentially also exacerbate a destructive systemic inflammatory response within the body, not unlike multi-resistant septicemia. 🤨😐
Its like a pandemic Ouroburos ring- predict it, create it, provide the faux solution that in fact actually creates it, that allows the prediction to come true, allowing the "solution" to be created again.🤦♀️🤦♀️🤦♀️
Fast forward 5 years from now, headlines read, "terrifying pandemic claims billions, survivors flee to protected "Gates" cities, for safety".😐🤐
Upside, mother nature only allows us to play dress ups "god" and trash her carefully crafted keystone species for so long, before she steps in.
Do those plasmid DNA fragments generate bacterial/viral peptides that will attract immunity or activate T killer cells? (Are they immunogenic?) What will happen if they are integrated into the genome of cells? Will those cells get killed off?
In an email I received in April, Sasha Latypova referred me here. From reading this article, I can see why she encouraged her readers to support your work.
I think this is a great introduction to the discoveries of Kevin McKernan. (In fact, I think these discoveries are so important that I hope to soon publish a Substack about them.)
That said, I did have some feedback:
1. I personally don't think of these injections as gene therapy. They may be classified as gene therapy, but in my opinion, they don't have any sort of therapeutic impact (except maybe a false sense of security).
2. The antibiotic concern you mentioned was exactly something I'd been wondering about: What if the plasmids, over time, become so parasitic that the host/recipient requires antibiotics, and are prescribed kanamycin or neomycin? (And what if those antibiotics wipe out some of their good, non-parasitic bacteria, leaving behind a higher number of the antibiotic-resistant parasitic bacteria?)
3. You said, “Australia is now 96% vaccinated (16+ 2 Doses)..."
Is the 16+ 2 a typo? I'm not sure what's meant by that.
Add to this the mRNA integrity issues, wherein the mRNA that is actually delivered in the NLP bubbles is not 100% accurate code for the spike protein. Some percentage is allowed by regulators to be imperfect, and code for unknown goo. According to the 2021 EUA email leaks from Europe, that percentage was on the order of 20-50% (!!!!!!).
Agree. From memory, in either Supply Contracts and/or reg public docs, active ingredient integrity minima were around 55%, begging many unanswered but highly obvious questions.
From memory, the EMA raised concerns about the level of viable mRNA in samples provided by PfizerL in support of its application for emergency approval. The solution? The threshold was lowered and the vaccine received emergency authorisation. Got that?
ship it!
Conditional marketing authorization. It is valid for one year. Nobody checked if it was renewed.
So essentially, given that we were already under a global antibiotic resistance emergency, to the point that the WHO's ARC advisory working group have determined a whole host of antimicrobials (particularly antibiotics) to be limited to the public, and held in emergency use only format, they have allowed the inhumane injection of multitudes with leaky, contaminated products, that not only migrate to the highly mitochondrial dense areas, but potentially also exacerbate a destructive systemic inflammatory response within the body, not unlike multi-resistant septicemia. 🤨😐
Its like a pandemic Ouroburos ring- predict it, create it, provide the faux solution that in fact actually creates it, that allows the prediction to come true, allowing the "solution" to be created again.🤦♀️🤦♀️🤦♀️
Fast forward 5 years from now, headlines read, "terrifying pandemic claims billions, survivors flee to protected "Gates" cities, for safety".😐🤐
Upside, mother nature only allows us to play dress ups "god" and trash her carefully crafted keystone species for so long, before she steps in.
So this is behind the increase in sepsis cases and deaths across all ages worldwide since 'the experiment' was rolled out?
Do those plasmid DNA fragments generate bacterial/viral peptides that will attract immunity or activate T killer cells? (Are they immunogenic?) What will happen if they are integrated into the genome of cells? Will those cells get killed off?
In an email I received in April, Sasha Latypova referred me here. From reading this article, I can see why she encouraged her readers to support your work.
I think this is a great introduction to the discoveries of Kevin McKernan. (In fact, I think these discoveries are so important that I hope to soon publish a Substack about them.)
That said, I did have some feedback:
1. I personally don't think of these injections as gene therapy. They may be classified as gene therapy, but in my opinion, they don't have any sort of therapeutic impact (except maybe a false sense of security).
https://tomrenz.substack.com/p/mrna-its-a-gene-therapy-and-they/comment/12503465
2. The antibiotic concern you mentioned was exactly something I'd been wondering about: What if the plasmids, over time, become so parasitic that the host/recipient requires antibiotics, and are prescribed kanamycin or neomycin? (And what if those antibiotics wipe out some of their good, non-parasitic bacteria, leaving behind a higher number of the antibiotic-resistant parasitic bacteria?)
3. You said, “Australia is now 96% vaccinated (16+ 2 Doses)..."
Is the 16+ 2 a typo? I'm not sure what's meant by that.
But otherwise, a great article.