To these questions, I found no other answer than, this is a giant experiment! Shared with the top management and political class of almost every state, who in turn exert strong pressure on their subordinates. In primis parliamentarians, magistrates, journalists, doctors and scientists.
Maurizio Blondet has repeatedly mentioned those famous 3000 that would maneuver the wires and the fate of the world. So I asked myself: If I were one of those 3000, what would I desire more than anything else? Money? Power?
No, money would not exist, I would create it. The Power to create money would give me absolute power over everything. What would I be looking for? What would scare me and make me similar to every other human being? Death.
So I asked myself: after the sequencing of human DNA and the enormous progress made in the ability to analyze fragmented data through AI and the progress made in nanotechnology, hasn’t someone finally discovered how to drink from the cup of the holy grail?

I subsequently, began to perform a brief search on the web for information regarding cellular aging. As a non-expert in the field, I learned that on October 5, 2009 the Nobel Prize in Medicine was awarded to Elizabeth Blackburn for her discovery of telomeres and the mechanism by which they protect chromosomes from degradation. After 2009 I discover that many researches on this subject start. There is a lot of scientific literature on the subject. From the discovery and drug testing of products that temporarily lengthen telomeres by activating the telomerase enzyme to gene therapies that permanently lengthen telomeres. In 2019, an American startup La Libella Gene Therapeutics promises to have found a way to rejuvenate human cells. It just happens to use a gene therapy vaccine, through a GMO virus in which a strand of mRna is inserted bearing the genetic instructions that cells need to produce telomeric reverse transcriptase (TERT). In addition to this startup, there are many pharmaceutical companies investing millions of dollars in telomere research, including Johnson and Johnson, which is investing $900 million in 2019.
These gene therapies bring with them, however, a number of adverse effects not yet documented. They need lots of mid- and long-term studies. They can cause cancerous formations or irreparably damage the cellular DNA and require many years of study, not to mention the fact that, in case of adversity with fatal outcomes, the trials would be promptly interrupted.
The cells of the human body have at conception an average of 15000 TTAGGG bases (Telomeres). At birth the average number is 10000 bases. At the age of 20 years approximately 8000 bases. Consider also that depending on a healthy lifestyle and some genetic predispositions, we can go to an estimate of loss from 35 to 150 pairs per year in adulthood. In some studies it is indicated that when reaching about 4000 telomeres, cells begin to become unstable and prone to premature death, the creation of degenerative diseases or cancer. Below this threshold, a sort of accelerated aging mechanism is established.
The average life span of cells varies from 15 years, for example of intestinal or skeletal rib cells, to 10 years of skeletal or muscle cells to about 1.3 years of liver cells. Do you understand, then, the complexity in addressing this problem without massive in vivo experimentation?
With engineered mRna, could they add or remove for example 35 TTAGGG pairs or remove 300 pairs with a dose of vaccine and add 300 with the booster, for the purpose of experimentation?
From a recent study: COVID-19 and DNA, the link between telomeres and intensive care: the study of Saint-Luc University Clinics and UCLouvain, the same virus, the Sars-Cov2 of artificial origin, as also admitted by Fauci, would seem to have interaction on telomeres, shortening them.
I’ve been trying for months to speculate on hypothesis after hypothesis in an attempt to answer why everything was so perfectly and maniacally designed back in 2014. They all fail and end up being illogical at some point. The only thesis left was the most nonsensical one….
I have, subsequently done more research to try to answer some questions.
1) Is it possible to study in detail what vaccines contain? No, they are protected by patents.
2) Is there a way to lengthen telomeres? Yes multiple.
3) Is there major funding for this? Yes countless as of 2014.
4) Is there any official trial evidence for these techniques? Yes countless, some I have listed.
5) Is there a way to collect data specific to portions of DNA via nanotechnology? Yes, the scientific literature on this is extensive.
6) Is there a valid motivation to research a way to be able to rejuvenate
human cells? Absolutely.
7) Could this technology be a valid element of corruption? I would say it is the most effective weapon that exists.
8) Are there any cases of important politicians, judges or scientists who have inexplicably changed their views on pandemic and vaccination? I would say countless.
Returning, then, to the famous 3000. If I were any of them, I could afford to wait 10, 20, 30 years or more, to have a gene therapy effective and safe to 99.9% that ensures me eternal youth? The answer would definitely be, NO! I am running out of time!
At that point, I would ask experts in the field, how to reduce this very long experimentation, and bring it for example to 2 or maximum 3 years. I would like to have a safe product right away, at any cost. I am offered the solution.
Such a rapid experimentation needs billions of volunteers, on which to test various gene therapies, various dosages, various combinations, single doses, double doses, various methodologies and to record short and medium term data, both on the effectiveness of the therapy and on any serious adversities.
Hence the traceability imposed between vaccine batch number and recipient of the same or double vaccinations. They are not the same type of vaccine. Each batch or group of batches probably corresponds to different dosages or different combinations, so as to have by the end of autumn a number of possible candidates to be used during the next vaccine booster, in order to get to select quickly 1 or 2 optimal candidates.
We come to the corruption of the high political and legal levels of the various nations. What immense power! The promise of eternal youth!
Every top level politician, general, president or dictator would firmly support big experimentation, indeed defend it at all costs.
The green transition and all this love for the future of our planet now makes sense! I’ve never met any of the famous 3000, but I’m convinced that in the past they never cared about the next one or what would be after their death. Now magically they are investing in their very own future! Clean air, resources.

There, I’ve come to the conclusion.
I hope that this can become a small stone thrown into the ocean, and that although my hypothesis seems crazy, it can serve to those more knowledgeable and better resourced, to be able to continue this search or pursue the search for truth. The time we have been given to understand is running out.
Most likely, mass experimentation will lead to the collateral death of an as yet unspecified number of people in the medium to long term. Simply because the ultimate goal is quite different. From a certain point of view, the adverse effects are crucial to better understand which formulation is the most suitable, for the famous 3000 elected people who will benefit.
Everything written, will be easily validated or disproved by December 2023. Until then, doubt about what we are experiencing will remain.
My whole thought started from a simple intuition, that I had while reading an article in which, it was talked about when the Roman generals returned to the city after a great feat, and it was whispered in their ear as a tradition the phrase “Respice post te. Hominem te memento”

Have a good day,
Enrico Fila.