IMPORTANT Video Transcript:

Reinette Senum interviews Dr. Sherri Tenpenny https://www.bitchute.com/video/x5YCfyuk9WoN/

Dr. Tenpenny details what Dr. Lee Merritt spoke of, a binary weapon. 22:42 mins. “I will make this military point. This is a perfect binary weapon.” https://ourgreaterdestiny.org/2021/01/mrna-vaccine-interview-with-dr-lee-merritt-vital-to-know/


12:33 mins We have never ever used [messenger] m-RNA in any vaccine. We have RNA vaccines. The measles vaccine in an RNA virus, the polio vaccine is an RNA virus. In those vaccines the virus is part of the vaccine wholly intact. So, when your body generates an antibody it’s against the outer coating proteins of that virus.

What we’re doing with this new virus is we’re taking a little piece of that viruses’ genetics specifically associated with a spike protein, and injecting that into the body creating a non neutralizing antibody, which in essence, instead of taking the m-RNA and gobbling it up and make it go away, this non neutralizing antibody creates antibody dependent enhancement referred to as ADE, which allows that little piece of m-RNA to start replicating on its own over and over and over creating these little pieces of virus spike proteins inside the body, for our body to create an antibody against.

This is what Bill Gates referred to when he said that ‘humans can become their own vaccine manufacturing machine’ because we interject m-RNA that binds to your reverse transcriptase enzymes and starts to replicate itself over and over creating antibodies against the spike protein. That spike protein has been shown in other very specific ways to cause injury.  

How m-RNA vaccines injure

The first mechanism is when you create an antibody to that spike protein. When we write about antibodies, they are designed in the literature to look like the letter Y.

The two arms atop the Y are called FAB fragments.

The stem of the Y is called the FAC fragment.

The two arms [FAB] grab hold of the virus and generally neutralize it.

When we look at the m-RMA, it grabs one arm of the Y loosely and binds to it. When the FAC fragment goes over to hook onto the macrophage that is supposed to kill it, and it gets taken inside, that m-RNA gets released and starts replicating over and over. It’s like having an ON button without an OFF button.

That whole mechanism just described is known as the trojan horse mechanism because it allows a piece of that virus to get inside your cells, start to replicate, and even get inserted into other parts of your DNA as a trojan horse. That’s one of 3 mechanisms.

15:55 mins The second mechanism is when you create this antibody, this non neutralizing antibody to the m-RNA, that stem or FAC fragment to that spike protein can actually go into your lungs and attach to the lung tissue and start developing what they call diffuse alveolar damage, which is diffuse injury to the cells inside your lungs where you breathe. It starts to break them down and destroy them. What those antibodies do is cause various degrees of pus, bleeding and damage to your lungs.

As you get this m-RNA vaccine, you create this antibody [Y], the antibody carries the thing inside the cells through a trojan horse mechanism, the antibody itself goes and starts to damage lungs.

16:50 mins The third and even more sinister mechanism. That spike protein antibody [Y] can attack your macrophages. There are 2 types of macrophages; Type 1 and Type 2.

Type 1 macrophages. Macrophages are a type of white blood cell that gobbles up the bacteria and viruses in your system that are not supposed to be there. They are your TH1 pathway, they are your hyper vigilant white blood cells. When we get bacteria in our body all day long from eating, brushing our teeth, going to the bathroom, having sex, cutting your finger, those white blood cells come along and gobble things up and make them go away.

When you get pneumonia or some serious infection the Type 1 macrophages are pro inflammatory. They show up at the infection, start creating cytokines, and blowing whistles, and bring in all the things to try and kill off the infection; very, very aggressive and highly inflammatory, which is what you want.

The Type 2 macrophages are anti-inflammatory so as you start to recover the Type 2 macrophages come in, tell the other guys to shut up, we’re here to clean up the mess. They clean up the dead debris of the tissue, the dead   white blood cells, etc.

The Type 2 and Type 1 macrophages work in concert. Type 1 kills off the infection and Type 2 heals it.

When you have this antibody to the spike protein [Y], which is the full intent and purpose of the vaccines, that antibody [Y] KILLS your Type 2 macrophages. It attaches to them and inactivates them.

In the experimental animals that actually died of lung infection and inflammation, when they sacrificed them, they found all the lungs had filled up with Type 1 pro inflammatory, highly cytokine types macrophages and zero Type 2 macrophages.

When they sacrificed the animals that had not been vaccinated but had been sick, what they found is that within 2 days of getting sick, without the antibody, without the vaccine, the Type 2 macrophages had come in to the infection and started cleaning up the mess and started healing it, as long as they didn’t have the presence of a spike antibody [Y]. It’s the presence of the spike antibody [Y] that killed them and didn’t allow them to do their job.

Those are 3 of 7 mechanisms the m-RNA vaccine is going to cause problems. To recap:

1] The antibody to the spike protein is going to destroy your lungs.

2] The antibody to the spike protein is going to loosely bind that virus or the m-RNA and drag it inside your cells through a trojan horse phenomenon, make it start replicating and have this process go on, and on, and on because it’s an ON button without an OFF button.

3] The antibody to the spike protein is going to shut off your M2 or anti-inflammatory macrophages.

Reinette: This is why you say people are going to start dying within a year,  year and a half.

Dr: When you look at all the studies that go back to 2002 of how they tried to develop a coronavirus vaccine, you get this antibody [Y] just floating around, looking for something to do, and then garden variety coronavirus shows up, and that’s what activates the whole process. It’s the re-exposure that leads to the antibody dependant enhancement and all this accelerated autoimmune disease.

There are 36 coronaviruses in the environment, 7 of them known to infect humans that have been around for 60 years. They were out there long before covid ever showed up.

So we’re going to get these non neutralizing antibodies [Y], coronavirus is going to show up, and it’s going to start killing people. 

Some people will die shortly after getting the vaccine however a large number of people are going to start to get horribly sick, get all kinds of autoimmune diseases, 42 days to a year out, and the doctors will likely diagnose it as a mutant strain and suggest they need extra doses of the vaccine.

This entry was posted in Uncategorized. Bookmark the permalink.