“Hacking The Software of Life” by information therapy in humans- a damningly dangerous development in human history: Dr. Samuel Maima

​By: Dr. Samuel Maima
MD Medline Pacific

The adenovirus  that was inserted into the structural genetic sequence was engineered by genetic engineers who were behind the production of Astrazeneca “experimental genetic material.”
In the replication region of the adenovirus, that replication region was excised and engineered genetically by genetic engineers who engineered the production of an altered viral nucleic acid sequence.
The vaccine was covered with micele, layers covered in lipids (fats).
What was the genetic code inserted into the replicating region of the “declared” adenovirus? This is something Prof Mola and the MESAC can explain what was the genetic coding or sequence that was engineered by the genetic engineers in the Asutrazeneca vaccine?

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If they can not explain what is the genetic code and it’s likely outcome on  specific cellular protein productions and it’s outcome on the human security of life like a “blindmen leading the blind”
But let me go on and explain the molecular interaction between the host and the disease causing agent or the foreign antigen or protein.
In this case, the Austrazeneca vaccine is a foreign material or agent with a DNA viral structure that was “altered”.
When foreign material (including those that potentiates disease development,) enters the human cells, and binds to the host cell membrane, the cell membrane polarity changes. 
The change in the polarity is sensed by the nano sensing peptides or proteins in the cell membrane.
The sensing by nano peptides spontaneously activate an inducible factor called “nuclear transcription factor (NT-kB). This is indeed a complex that resides in the cells’ cytoplasm.
This complex is found in virtually all differentiated human cells. 
NK-kB transcribes more than 500 genes that causes diseases in humans. It also transcribes more than 400 inflamasomes that cause inflammation. 
Activated NT-kB is responsibe for disease developments, immune activation and inflammation.
When NT-kB is activated, it leaves the cytoplasm and translocates into the nucleus where its binds to the target DNA. The supervisory molecular is messenger ribonucleic acid (mRNA).
Whilsts in the nucleus of the cell, its transcribes the genetic coding for the specific protein to be produced by the ribosomes.
When the genetic sequence or transcription is completed it leaves the nucleus and the genetic message (codings) are presented to the ribosomes by transfer RNA (tRNA). In the ribosomes, the ribosomal RNA transalates the coding message and supervises the production of specific protein for the disease causing agent to be fed and grow the disease causing agent in the host cell.
After production of the specific protein is done, a last process is called “post translational modification”. This is under the care of histone (de)acetyltransferase enzyme to make sure perfection is done so that perfect specific protein is produced for the disease causing antigen is produced.
Only the Astrazeneca genetic engineers knows what genetic code was inserted into the DNA viral sequence that is the replication zone of adenovirus - a DNA virus..
I would assume that Prof Mola and the members of MESAC knows the genetic codes that was inserted into the DNA sequence of adenovirus in the replicating zone and what specific protein it would be produced using the host protein producing cellular machinery. Some say it a “spike protein” but we donot know.
How can MESAC conduct the molecular evaluation on those who receive the vaccination and provide the account on the basis of the genetic codes that was inserted into the replication zone of the DNA of adenovirus into the human cellular host?
They don’t have the molecular and biochemical technical expertise and the resources to do that on those who would receive vaccination. There should be the institution of monitoring and evaluation biochemically on those who volunteered with an “altered viral material” to appreciate whether or not they would visualize “spike protein”.
In my view, Astrazeneca and mRNA vaccines are basically hacking the information operating of the human genetic system by men towards “human disaster of scale and magnitude.”
According to the study by New York-based Sloan Kettering Cancer Centre, the mRNA vaccine and altered viral DNA sequence in Astrazeneca vaccine has the potential to interact with cancer producing genes or proteins and suppressing tumor proteins in the cell cycle. This alone must alert us.
Both the mRNA vaccines produced by Moderna and Pfizer and altered Astrazeneca vaccines are “experimental gene therapies” approved by FDA for emergency use authorization (EUA) only until 2023. 
Yet, the Government, media and corporations including some established collaborative scientific and medical institutions are promoting them as if they are gurranteed safe. This include MESAC.
The systemic deception will, in my opinion, will ended up being judged in the rear-mirror of history as one of the most wreckless acts of medical treachery ever committed against the human race.
I wonder whether MESAC including Prof Mola knows what they are talking about when they gave the endorsement to allow the delivery of vaccines into PNG.
What if the “genetic coding” that was inserted into the replicating DNA region of adenovirus results in the protein production that suppress “tumor suppressing proteins that regulate and control cancer developments in humans?
What if protein production can initiate the production of autoimmune antibodies?
For the uncertainty that is herald by the rapid production and non declaration by the genetic engineers of genetic codes inserted into the replicating region of the DNA of adenovirus by the genetic engineers of Astrazeneca vaccines.
Under the  International Nuremberg Code, acceptance of an “experimental gene altering vaccine” without “prior informed consent” on humans who have soul, bodies and free wills by MESAC without wider scientific and medical consultation will haunt them. It will haunt them.
During the pandemic or when you have virus in the population, it is not an appropriate time to vaccinate with a viral constituents because there is huge propensity for the development of recombinant mutagenic viral variants. 
It is not surprising when there is evolution and the development of recombinant mutagenic variants strains have been mentioned lately. It has the propensity towards developing very infectious strain that would kill more people. It is for this reason that it is imperative not to give vaccines with viral constituent during pandemics.
For this reason, there is an ongoing announcement  by Bill Gate that the third wave of coronavirus will be highly pathogenic. He exactly knows what he is talking about as a non medical and scientific person. How does he know it?
It is better that human subjects are exposed to develop natural/herd immunity but why there is an aggressive and vigorous vaccine push globally is “highly suspicious”.
Transhumizing agenda by rewriting the information software of life is basically hacking the information software of life. 
Think about it for a while.

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