How exhausting to the body continually replicating antibodies to hidden spike proteins must be. How mind boggling Medical Professionals who should understand this but don’t are to those of us who formerly trusted their judgment.
I can’t imagine what the next five years will look like for any of us.
Its almost as if the vaccine is actually the disease. Maybe that is why it was patented before the v rus was patented? Btw, since when do folks patent a “deadly” virus. Is this kosher?
If you read the “DEFUSE” proposal from EcoHealth to DARPA (the one rejected because DARPA considered it too dangerous, but later funded by NIAID), they (EcoHealth et al) appear to have been collecting bat viruses, deciding which ones were most likely to infect humans, make them more transmissible, and then make vaccines to supposedly reduce the threat of these viruses (both natural and man made).
Some of these ‘vaccines’ were even supposed to be aerosolized and sprayed into bat caves.....to see what happens (I’m not kidding, they didn’t use those exact words in the proposal, but that’s what they meant).
DARPA refused to fund this stupidity for good reason.
In short, they appear to have been building new viruses, or changing already existing ones, and creating new (untested) vaccines against these viruses.
They then patented the viruses and vaccines.
When it got out, or the Chinese government released it, they used the untested vaccines......
This is good stuff, Mark. Thank you! This research may be helpful to Jeff Childers’ Covid Accountability Project. I will be sure to share this with the right folks over at C&C. Do you follow him on Substack? If not, I highly recommend you join the C&C army! 😉
As usual, you express your points in a very easy to understand manner. It makes it easier for me to share with others (whether or not they want to listen).
That’s because it is complete and utter crap. To any student of mRNA science and basic immunology, this is all nonsense. Kevin is a retired chiropractor who I imagine was not loved as a child. It is an outrageous and insulting to someone who has 4 years of medical school, 3 years of residency, an MPH degree and over 20 years of emergency medical clinical experience to see snake oil salesmen like Kevin get such audiences. It only makes my job harder.
As a student of mRNA science, explain to everyone how the protein made by the mRNA in the shot can protect anyone. This is basic immunology, as you said. The mRNA is making something similar to the spike protein on the virus that has been mutated. The antibodies your body will make against that protein created from the shot will be suboptimal against the protein on the mutated variant viruses. The shot induced antibodies are non-neutralizing, and will enhance not only the infection but the disease itself. That's why people who get injected keep getting infected. Right, Fauci? How many times have you been injected and you still get infected?
Thank you for this concise description: "This is done by natural killer cells and activated T-cells. It is very precise and clean and does not result in huge amounts of inflammation, nor does it destroy normal myocardial cells nearby. These cases will resolve to normal homeostasis." Isn't the human body and God-given immune system amazing? Why would anyone want to interfere in that supernatural, miraculous design? Hmm
You have 15 quintillion proteins of about 30 varieties circulating in your body fluids at all times. This is the complement system. When it gets activated, it's like throwing one lighted match into a box of matches, it takes off fast and is called the complement cascade. It is very destructive and hyperinflammatory. It will attract white blood cells to all cells of the body that are either making spike proteins or have spike proteins attached. It is very aggressive and has a cellular membrane attack system that will destroy normal healthy cells nearby. It is the heavy artillery of the immune system and is reserved for special occasions when the immune system is having a hard time getting rid of something that should not be there.
The reason it gets activated is because the immune system already made antibodies against the spike protein after the first shot. The idea is that these antibodies will immediately intercept the spike protein on the virus if you get infected and maybe lessen your symptoms. But what is the second shot or booster shot doing? It is causing the production of BILLIONS more spike proteins that should not be happening. It is able to happen because the mRNA message to make these spike proteins is HIDDEN inside of lipid nanoparticles. The immune system can't see it until the spike is being produced. If it was a natural infection from a virus, the immune system would be able to see the spike. That's the difference. So now, your body is making billions of spikes, the immune system gets pissed off and activates the destructive complement cascade. When it happens in the heart, that results in myocarditis, which can be deadly and result in Sudden Adult Death Syndrome.
This so-called "C-virus" has NEVER existed!!! There are NO pathogenic viruses - it is always searched only for nucleic acid fragments/nucleotides and these occur in all living beings and plants whether alive or dead - this whole building of lies is built on a pseudo-science with which the so-called "virologists" supply potential victims to the pharmaceutical industry - a highly criminal act and this already for almost 200 years - a global disgrace!!!!
Both the EcoHealth proposal to DARPA called "Understanding the Risk of Bat Coronavirus Emergence" and the USAID funding are things I am reading about in Dr. Andrew Huff's book, which I am slogging through.
That proposal was cleverly worded to avoid the appearance of the GoF research for which it is intended. The problem with the book (among other things) is that Huff's timeline isn't always explicit, so it's possible that I'm not caught up yet to anything he may write about DEFUSE.
The DRASTIC website layout is a bit tough to follow, but I found the DEFUSE PDF on Intercept and am looking through it.
You really should follow Jeff Childers. He is a Florida attorney who has defended a number of mandate victims - from people who lost their jobs or businesses to those who died needlessly or are vaccine injured. Jeff has a vision to build an online accountability database of facts, strictly facts, related to those who need to be held accountable for the past three years of death, injury and economic breakdown.
The lipid nanoparticle that is injected is a fat bubble made with cholesterol and DSPC, normal body fats, so it can merge with just about any cell it bumps into to deliver the payload. Polyethylene glycol is used not only to keep the particles separated, but to determine the size of the particle, which is designed to be almost exactly the same size as the original virus particle.
The payload it delivers into the cell is more fat bubbles, tinier ones. These fat bubbles self assemble in manufacturing because the strand of manmade modified messenger RNA is negatively charged and the proprietary fat bubble is positively charged. Pfizer uses ALC-315 and Moderna uses SM-102 as the fat bubbles. The idea is for the ALC-315 or SM-102 to react to the acidity of the cytoplasm and release the mRNA. The mRNA will then translate into a proprietary protein that is similar to the spike that was on the original virus. The protein is then released from the cell.
After this translation happens, there is an enzyme called RNase that is supposed to break down the mRNA. Due to the pseudouridine they put in there to replace uracil, this doesn't happen nearly as quickly, so the mRNA strand can keep making the proteins. This is by design, because they think the protection is in antibodies, so they want as many spike proteins as possible to produce as many antibodies as possible. As you stated, how long the mRNA persists before it is totally broken down, no one really knows for sure. Some say it could be months.
Sometimes the ALC-315 or SM-102 does not break down in the cell and can end up being deposited in tissue like the ovary and become toxic. We know that happens because Japan attached luciferase to SM-102 so see where it would go in rats, and its bioluminescence showed up in the ovaries.
Sometimes the mRNA or smaller parts of it called microRNA gets excreted by the cell in exosomes. These can persist for a very long time in nerve tissue and can disrupt interferon signaling between immune cells. This could explain immune suppression after the shot.
Not a scientific answer, but it obviously stays in the body a hell of a lot longer than advertised.
Last I heard, the spike protein initiated by the mRNA could be detected in the body for up to 15 months (the duration of the study). I’m not sure about the mRNA itself......
How exhausting to the body continually replicating antibodies to hidden spike proteins must be. How mind boggling Medical Professionals who should understand this but don’t are to those of us who formerly trusted their judgment.
I can’t imagine what the next five years will look like for any of us.
Kevin is not a real doctor and profits off people like you. Some of us spent years studying this stuff and are insulted by quackery like this
I challenge you to an open debate any time, anywhere, any platform.
Why not publicly debate him?
Or are you too scared to do that?
😉
Its almost as if the vaccine is actually the disease. Maybe that is why it was patented before the v rus was patented? Btw, since when do folks patent a “deadly” virus. Is this kosher?
If you read the “DEFUSE” proposal from EcoHealth to DARPA (the one rejected because DARPA considered it too dangerous, but later funded by NIAID), they (EcoHealth et al) appear to have been collecting bat viruses, deciding which ones were most likely to infect humans, make them more transmissible, and then make vaccines to supposedly reduce the threat of these viruses (both natural and man made).
Some of these ‘vaccines’ were even supposed to be aerosolized and sprayed into bat caves.....to see what happens (I’m not kidding, they didn’t use those exact words in the proposal, but that’s what they meant).
DARPA refused to fund this stupidity for good reason.
In short, they appear to have been building new viruses, or changing already existing ones, and creating new (untested) vaccines against these viruses.
They then patented the viruses and vaccines.
When it got out, or the Chinese government released it, they used the untested vaccines......
That’s why they were ‘developed’ so quickly......
Sometimes you read a theory and it rings true... like a liberty bell.
So EHA was also working on the vaccines? I did not know that. Also, I read that USAID funded the research as well, not just NIH.
That’s what was in the proposal.
See DRASTIC research at :
https://drasticresearch.org/2021/09/21/the-defuse-project-documents/
Or search for DRASTIC, which is a group of people from around the world who are looking into the origins of Covid 19.
They have collected a huge amount of real evidence, not just theories, regarding the origins of Covid.
Included is the DEFUSE grant request from EcoHealth, the DARPA rejection letter, and much more.
This information was exposed a while back and made a lot of waves.... but as usual, no action by anyone who has the power to do something about it.
This is good stuff, Mark. Thank you! This research may be helpful to Jeff Childers’ Covid Accountability Project. I will be sure to share this with the right folks over at C&C. Do you follow him on Substack? If not, I highly recommend you join the C&C army! 😉
Thank you and I’ll look it up.
I thought that everyone already knew about the ‘Defuse’ proposal and it’s aftermath.
I never thought about all the people who got involved with this stuff after this was exposed and have never heard of it.
At the time this information was released, it was considered a ‘smoking gun’ regarding the origins of Covid.
And then nothing happened....
Continue sharing your research...
As usual, you express your points in a very easy to understand manner. It makes it easier for me to share with others (whether or not they want to listen).
That’s because it is complete and utter crap. To any student of mRNA science and basic immunology, this is all nonsense. Kevin is a retired chiropractor who I imagine was not loved as a child. It is an outrageous and insulting to someone who has 4 years of medical school, 3 years of residency, an MPH degree and over 20 years of emergency medical clinical experience to see snake oil salesmen like Kevin get such audiences. It only makes my job harder.
As a student of mRNA science, explain to everyone how the protein made by the mRNA in the shot can protect anyone. This is basic immunology, as you said. The mRNA is making something similar to the spike protein on the virus that has been mutated. The antibodies your body will make against that protein created from the shot will be suboptimal against the protein on the mutated variant viruses. The shot induced antibodies are non-neutralizing, and will enhance not only the infection but the disease itself. That's why people who get injected keep getting infected. Right, Fauci? How many times have you been injected and you still get infected?
Thank you for this concise description: "This is done by natural killer cells and activated T-cells. It is very precise and clean and does not result in huge amounts of inflammation, nor does it destroy normal myocardial cells nearby. These cases will resolve to normal homeostasis." Isn't the human body and God-given immune system amazing? Why would anyone want to interfere in that supernatural, miraculous design? Hmm
What is a complement cascade?
You have 15 quintillion proteins of about 30 varieties circulating in your body fluids at all times. This is the complement system. When it gets activated, it's like throwing one lighted match into a box of matches, it takes off fast and is called the complement cascade. It is very destructive and hyperinflammatory. It will attract white blood cells to all cells of the body that are either making spike proteins or have spike proteins attached. It is very aggressive and has a cellular membrane attack system that will destroy normal healthy cells nearby. It is the heavy artillery of the immune system and is reserved for special occasions when the immune system is having a hard time getting rid of something that should not be there.
The reason it gets activated is because the immune system already made antibodies against the spike protein after the first shot. The idea is that these antibodies will immediately intercept the spike protein on the virus if you get infected and maybe lessen your symptoms. But what is the second shot or booster shot doing? It is causing the production of BILLIONS more spike proteins that should not be happening. It is able to happen because the mRNA message to make these spike proteins is HIDDEN inside of lipid nanoparticles. The immune system can't see it until the spike is being produced. If it was a natural infection from a virus, the immune system would be able to see the spike. That's the difference. So now, your body is making billions of spikes, the immune system gets pissed off and activates the destructive complement cascade. When it happens in the heart, that results in myocarditis, which can be deadly and result in Sudden Adult Death Syndrome.
Thank you for explaining!
This so-called "C-virus" has NEVER existed!!! There are NO pathogenic viruses - it is always searched only for nucleic acid fragments/nucleotides and these occur in all living beings and plants whether alive or dead - this whole building of lies is built on a pseudo-science with which the so-called "virologists" supply potential victims to the pharmaceutical industry - a highly criminal act and this already for almost 200 years - a global disgrace!!!!
https://maryann255.substack.com/p/the-truth-is-always-on-the-other-20e
https://maryann255.substack.com/p/the-truth-is-always-on-the-other-01f
https://maryann255.substack.com/p/the-truth-is-always-on-the-other-f29
https://maryann255.substack.com/p/the-truth-is-always-on-the-other-5cc
https://maryann255.substack.com/p/the-truth-is-always-on-the-other-c6f
https://maryann255.substack.com/p/the-truth-is-always-on-the-other-228
https://maryann255.substack.com/p/the-truth-is-always-on-the-other-c6f
https://maryann255.substack.com/p/the-truth-is-always-on-the-other-c2c
Both the EcoHealth proposal to DARPA called "Understanding the Risk of Bat Coronavirus Emergence" and the USAID funding are things I am reading about in Dr. Andrew Huff's book, which I am slogging through.
That proposal was cleverly worded to avoid the appearance of the GoF research for which it is intended. The problem with the book (among other things) is that Huff's timeline isn't always explicit, so it's possible that I'm not caught up yet to anything he may write about DEFUSE.
The DRASTIC website layout is a bit tough to follow, but I found the DEFUSE PDF on Intercept and am looking through it.
You really should follow Jeff Childers. He is a Florida attorney who has defended a number of mandate victims - from people who lost their jobs or businesses to those who died needlessly or are vaccine injured. Jeff has a vision to build an online accountability database of facts, strictly facts, related to those who need to be held accountable for the past three years of death, injury and economic breakdown.
This is a good starting point where he lays out his whole plan: https://www.coffeeandcovid.com/p/c-and-c-news-friday-october-28-2022
The lipid nanoparticle that is injected is a fat bubble made with cholesterol and DSPC, normal body fats, so it can merge with just about any cell it bumps into to deliver the payload. Polyethylene glycol is used not only to keep the particles separated, but to determine the size of the particle, which is designed to be almost exactly the same size as the original virus particle.
The payload it delivers into the cell is more fat bubbles, tinier ones. These fat bubbles self assemble in manufacturing because the strand of manmade modified messenger RNA is negatively charged and the proprietary fat bubble is positively charged. Pfizer uses ALC-315 and Moderna uses SM-102 as the fat bubbles. The idea is for the ALC-315 or SM-102 to react to the acidity of the cytoplasm and release the mRNA. The mRNA will then translate into a proprietary protein that is similar to the spike that was on the original virus. The protein is then released from the cell.
After this translation happens, there is an enzyme called RNase that is supposed to break down the mRNA. Due to the pseudouridine they put in there to replace uracil, this doesn't happen nearly as quickly, so the mRNA strand can keep making the proteins. This is by design, because they think the protection is in antibodies, so they want as many spike proteins as possible to produce as many antibodies as possible. As you stated, how long the mRNA persists before it is totally broken down, no one really knows for sure. Some say it could be months.
Sometimes the ALC-315 or SM-102 does not break down in the cell and can end up being deposited in tissue like the ovary and become toxic. We know that happens because Japan attached luciferase to SM-102 so see where it would go in rats, and its bioluminescence showed up in the ovaries.
Sometimes the mRNA or smaller parts of it called microRNA gets excreted by the cell in exosomes. These can persist for a very long time in nerve tissue and can disrupt interferon signaling between immune cells. This could explain immune suppression after the shot.
https://www.sciencedirect.com/science/article/pii/S027869152200206X?via%3Dihub
Yeah, it's still an experiment.
Not a scientific answer, but it obviously stays in the body a hell of a lot longer than advertised.
Last I heard, the spike protein initiated by the mRNA could be detected in the body for up to 15 months (the duration of the study). I’m not sure about the mRNA itself......