THE MANY LIES THAT SOLD COVID GENE THERAPY TO THE WORLD
1. These genetic vaccines are not gene therapy.
2. These shots stay in the arm and do not go far from the injection site the deltoid muscle.
3. Mod RNA mRNA from the covid vaccines break breaks down rapidly in the cell.
4. The genetic vaccines or Spike protein cannot enter the nucleus of the cell.
5. MRNA cannot be reverse transcribed to DNA and integrate into the genome.
6. There is no DNA in the vaccines which could change your DNA.
7. The shots only cause the creation of the spike protein not other proteins.
8. There are no other existing safe and effective treatments for SARS-COV-2.
9. The covid shots are effective at preventing death and severe disease.
10. They do not shed to others.
All of these were lies.
COVID genetic vaccines are Gene Therapies--
* Synthetically modified genetic sequence coding for the foreign viral Spike protein is delivered to cells in LNP where it will direct the body to make and express the foreign Spike Protein on the cell surface where your body will mount an immune response to the foreign protein and attack and destroy those cells--your cells.
* Pfizer and Moderna SEC filings and patents listed this technology as gene therapy
WHY GENE THERAPY DID NOT MAKE IT TO MARKET IN OVER 30 YEARS OF RESEARCH
1. They caused lethal cancers (mostly leukemias) through integrating into host DNA through insertional mutagenesis.
2. They cause lethal autoimmune reactions.
3. There was the risk of inadvertent Gene transfer to progeny of the gene therapy made it to the testes are ovaries--recipients were sterilized to prevent this early on.
4. In short--risk was only worth reward for otherwise lethal disease.
Nancy M.P. King, "Accident and Desire: Inadvertent Germline Effects in Clinical Research," Hastings Center Report 33, No. 2 (2003): 23-30
LIPID NANO PARTICLES--THE DELIVERY SYSTEM
* Cloaks and protects the MRNA from the immune system where it would be attacked and degraded.
* Allows the genetic sequence to cross the cell and nuclear membrane where it's payload is deposited.
* Lipids themselves are toxic; some not approved for human use.
These lipids allow the vaccines to go to every organ in the body-- to the brain, to the heart, to the lungs, to the testes, to the bone marrow, to the ovaries preferentially, the salivary glands, muscles, skin, everywhere in the body, the heart . . . more was actually found that there was spike protein expression in the brain of someone who who died a lethal brain disease 9 months out from the last vaccine. So these are lasting the lipids have toxicity themselves in fact the SBC has caused
LIPID AND PEG TOXICITIES--INTRINSICLY UNSAFE
* LNP's by themselves can be intrinsic toxicity especially positively charged
* DSPC has caused nervous system impairment, liver damage, embryo/fetal damage and is confirmed animal carcinogen according to manufacturer Safety Data Sheet SDS (Avanti Polar Lipids, Inc., May 15th 2018)
* 72% of people are estimated to have antibodies to polyethylene glycol "PEG," (Lai, 2016)
* Cancer drug, Doxil with PEG and anticoagulant containing RNA and PEG in 2014 caused severe anaphylactoid reactions to PEG including death for the latter (Jop De Fries, 2020).
THE WAY THAT THESE ARE MODIFIED. THEY DON'T BREAK DOWN
The modRNA with N1 methyl pseudouridine does not break down quickly and mRNA can be reverse transcribed to DNA
* Long-term presence of artificially stabilized mRNA either whole or in partially degraded fragments could lead to:
1. long-term expression of the spike protein as well as;
2. increased risk for reverse transcription to DNA and possibly:
A. Direct genomic integration causing site-directed mutagenesis leading to cancers and or;
B. Cause inheritable changes in progeny through sperm and egg uptake and alterations.
