A Crime of Monumental Significance

Why antidotes to the spike protein may not help.

Has everyone heard about the DNA contamination in the Vaccine vials? It is in there because the vaccine manufacturers cut corners to save money.

Corporations tend to do this when they are granted blanket immunity by the government.

Summary with how they got away with this. I could write 20 pages explaining this in detail but I’m going to do it in one page so I don’t lose those of you who aren’t familiar with the terms and processes.

The amplification of the modRNA strands used in the vaccine product presented to the FDA to get EUA was accomplished using a copying method known as “Polymerase Chain Reaction”. (Yes, this is the same PCR that is used for testing).

Amplification by PCR does not require DNA plasmids and bacteria so it is DNA contamination-free.

Even though the manufacturers committed wholesale fraud during these “PCR Trials”, the FDA approved the vaccine for use.

That was the point the Manufacturers switched the process of amplification that uses DNA plasmids inserted into E. Coli bacteria to make the trillions of strands of modRNA needed for the vaccine vials that would be given to the whole world. They switched because, 1) amplifying by the PCR method is way more expensive and they already had their EUA and 2) The E. Coli method is way faster and, remember they were in a big hurry, right? (to save the world from a deadly pandemic, that could be the “once-a-century pandemic we’ve all been waiting for” according to Bill Gates THAT ACTUALLY WAS, AS I TOLD DR. BHATTACHARYA “THE BIGGEST NOTHING BURGER TO EVER HIT THE AIRWAVES”, having derived the IFR for all ages on March 8, 2020 to be the same as the seasonal flu at .1%. You see, this was all perfect. If anyone called the vaccine manufacturers out on using a product that was all contaminated and never tested, they could always say, “We had to use the E. Coli method. It was an EMERGENCY! WE HAD TO MOVE AT THE SPEED OF SCIENCE!

Roughly, the way amplification using E. Coli works is:

1. Make a DNA plasmid that contains the spike protein sequence and a some other sequences important to the manufacturing process but not relevant to this discussion.

2. The plasmids are in the form of a ring of DNA and treated E. Coli will take them in readily.

3. Then you throw the E.Coli containing the plasmids into a big vat of nutrient broth and set it at the optimum temperature for replicating.

4. In about 4 days, you’ve got trillions of E.Coli in the vats.

5. Extract the plasmids from the trillions of E. Coli by treating the vat contents with chemicals

6. cut the rings.

7. add enzymes to the cut plasmids (of DNA) to transcribe them into RNA.

8. filter the mixture to get rid of the DNA fragments and rings that survived the cutting

9. Modify the purified RNA into the product you want to put in the lipid nanoparticles

10. inject the lipid nanos containing the RNA into people’s arms

Evidently, they didn’t do step 8.

Kevin McKernan of the MIT-Harvard Broad Institute and Medicinal Genomics sequenced some of the vials and found they contained, of the vial’s genetic material, 35% in the form of DNA.

Is that too much?

The European Medical Agency (Europe’s FDA) places the upper limit of what DNA contamination is acceptable at .033%. The vials Pfizer and Moderna stuck into the public’s arms had 1000x more DNA than was acceptable.

Here’s the problem. That DNA can get into the nucleus of your cells. When transcriptase (the enzyme found in the nucleus that makes RNA from DNA ) works on the DNA that’s in all of us under ordinary circumstances every day, there is no reason it won’t work on the DNA plasmids floating around in your nucleus too.

Unlike, RNA which doesn’t last long (hours, maybe days (at least the RNA that doesn’t have psuedo-uridine in it)), DNA is forever.

Treating yourself with something that might be an antidote to the spike protein- these things like Nattokinase that are selling like hotcakes although they haven’t been proven to work- is not going to help if you make spike protein forever. If the DNA segments incorporate into your gametes, you’ll pass this process on to your offspring. If you listened to the podcasts I did last week with Dr. Harvey Risch, you know this stuff damages your immune system 10 different ways.

Why didn’t the FDA notice this and say, “Your dirty stuff is 1000x too contaminated with DNA. Spend some money and filter the mixture properly. And by the way, you have to test it too.” We might not ever know.

A Classic “Bait and Switch”

The stuff that was used in the trials, that got EUA, was PCR-derived. The stuff they injected into the public starting on December 14, 2020 was E.Coli-derived. So basically, the E.coli-derived modRNA was never tested. It was a classic “Bait and Switch”.

…except for 502 trial participants… This tiny group got the E.Coli-derived stuff when they went through the trials. Did they do worse than the PCR-derived modRNA participants?

YES, WAY WORSE. Someone, just recently, found their results hidden away in the data. There were 250 controls (who got the placebo) and 252 who got the E.Coli-derived vaccine. A whopping 2.4 times (155 vs 65) as many participants getting the vaccine experienced adverse events compared to the group who got the placebo. But they gave them to the public anyway.

NO WONDER THE FDA WANTED TO HIDE THE TRIAL RESULTS FOR 75 YEARS!