This short viewpoint by me seeks to drive some debate here and derive your views & underscores why POTUS Trump MUST put hard STOP on mRNA technology USAGE until the proper safety research is completed
as you read, you can see my goal was not to be complicated, no fancy biochemistry, just my 50,000 foot view on this mRNA technology and what I think is needed now. to drive debate and in my words, no one wrote this for me...there has been a move now among some substack writers to have people write their work and they pay them to. it is becoming clear who writes what...even in substack it is becoming a quasi-fraud. again, the public always loses. we have commentors on stack who we do not know real identities and some writers who do not write their own work. ugh
Frankly, if someone says the "right" thing based on solid research, I don't care who posts it. We need all the help we can get to get people to pay attention because we need all the people we can get to expose and share the truth. PS: Although I really like the words YOU wrote, especially when you're angry - lol
I agree with you but they're not going to stop this vaccine or any others they're working on because it's the depopulation plan from the WEF. Next step is to force vaccination. Washington state wrote and passed laws recently to do just that using police and military if necessary in a future
pandemic (actually plannedemic). Dr Ana Maria Mihalcia's recent substack has all of the Washington state law. She lives in Washington state. No doubt all blue states will follow Washington state. God save us.
I find it strange that you keep calling Trump the president of the United States when he is not and he has no intention of stopping any va€€ines as he is part of the system (WEF)
Also the mrna va€€ines are doing exactly as intended except maybe it's not doing as much harm as they would like
I present to you personally an honest fellow quite astute with the initials JR who I think you may know. He is my reference, we live not far apart. He knows all about my existence. Just ask him anytime.
It’s more than 40 year old cell transfection reagents in a seriously off-label use to infect healthy cells with viral genes.
That’s ALL it is.
How do I know?
Because I regularly used those same cell transfection reagents starting back in the 1990s in my labs in my doctoral and post-doc research.
It was a completely trivial process even back then. The only difference are that these guys are using it in a way that no IRB in any university would have approved.
this is the key, thank you for sharing this critical information Gregorio, we are not experts in this and it is important folk like you share your expertise.
And thank you, Paul. Also, given how critical small numbers of progenitor cells are in development (but also in adult stem cell populations), a product capable of whacking these cells is capable of deranging downstream developmental pathways. Two obvious outcomes to expect would be an increase in miscarriages and immune system and blood problems (most of which cells come from the hematopoietic stem cell population).
You are correct Doc. My words to the damned CYSTem is flock off because I will never accept the D&D jab. (death and destruction) They can shove it up their ample asses.
this is very troubling and I have been reading...so how do we handle this? to table it means he hit Vance...we are in such a shit situation for we cant let Harris et al near the chair but Vance got to explain this...is it just about money to these people?
There is no safety with mRNA LNP technology. It’s bio weapon technology that they intend to keep using. Just ask JD Vance. And all the other players salivating over their future profits. They don’t give two shits about our safety.
Agree with many of your points. However, Robert Malone, who created the mRNA technology, has not been silent. He warned his colleagues of the dangers and problems with it but they ignored him and went forward. He has always been outspoken about the dangers of that technology.
thanks for being here. hugs, respect....there is a reason why Malone stayed silent for so long...he did not warn anyone, he was silent UNTIL he could be no more...he shilled the shots...the trail is there. but note I state 'oaths'...proper courts...it is there that the truth emerges. not congress or no dog and pony bullcrap we have been subjected to. then tell your friend Robert et al. to interview with folk like me, McCullough et al. Couey, Yeadon...he wont because he cannot defend his actions. sorry that you believe that crap he sold you. I have no issue with him personally, its just that he is a fraud and took people's money based on lies and his work killed people. if Bourla, Fauci, Birx, Bancel et al. are to be investigated, he must be too. not because you 'like' what he sold means we go with that. no...he is as culpable and proper hearings can decide the extent. and if there is to be consequences...he moves like Biden and Kamala, reads from phones and teleprompters for there are legal issues involved in his words and also, he wont talk to the right people. for now.
Yes Sue he did - BUT he only spoke out when it became obvious it was harmful. He in fact, had little to do with the whole project, but tried to claim fame when everyone (except myself, Dr Alexander et Al) thought it was a miracle cure. As soon as the VAERS reports began stacking up, that snake in the grass jumped ship and pretended to be a whistle blower and no longer claimed he “invented” mRNA technology. Because his colleagues had long since outed him as a fraudster anyway!
Many “X”ers and sub-stackers have labeled him “controlled opposition” but just personally, I don’t think he’s that clever m, he is just an everyday coward running from the part he played in ruining millions of lives!
Sorry but he belongs up on the g@ll0ws right beside Fauci!!!!
I agree...but we always have proper hearings first. but he is a con artist...and how you stated it is exactly how it has played out. he wanted money on upside selling it and on downside when the shit hit the fan
Does Malone write his own stuff? Some substacks are probably written by AI, just like scientific journal articles. It would be interesting to know what JD Vance's perspective is on Malone, given AmplifyBio's role in promoting mRNA therapeutics.
Malone used the EXISTING procedures and reagents of cell transfection to develop a particular in vivo use in an attempt to counteract the effects of mutated proteins in a transient fashion, either to outcompete with normal gene products the products of a defective protein that resulted in a disease state or to silence that expression of the defective gene, either of which, depending on the condition, had at least the theoretical possibility of restoring at least some function and reducing the disease phenotype.
He was not to cell transfection what Kerry Mullis was to PCR.
The cell transfection reagents began as attempts to introduce therapeutic agents directly into the cells of diseased tissue. This was a noble attempt. Why? Because while chemotherapy works, it works by killing cancer cells at a more rapid rate than non-cancerous cells--but it still whacks normal cells.
The hope was to design cancer cell-specific reagents that would target ONLY cancer cells, perhaps targeting a cell surface receptor or other cell surface protein unique to cancer cells. This way a very small amount of the therapeutic agent could be targeted only to where it was needed, sparing healthy cells and also reducing the amounts needed of very expensive drugs.
The problem? At that time, at least, they couldn’t get specific enough. But someone else figured out that they were great vehicles for delivering exogenous genes into cell without killing them, expressing exogenous proteins in those cells, and being able to study the expression and behavior of those proteins in the context of a living cell. And, so, the era of modern molecular biology was born.
With the extreme ease via PCR and the use of a huge variety of restriction enzymes (acquired from bacteria that used them to chop up the DNA or RNA of invading viruses), it was possible to identify by the use of point mutations as well as insertion or deletion mutations or chimeric mutations, the functional regions of particular genes. But the way of seeing the effects of those deliberate mutations was to see how those proteins behaved inside of cells.
And those cells used were any of a variety of immortal cell lines. The benefit of using them was that they had been fully characterized and that they were monocultures of cells that had no innate or adaptive immune system activity to screw things up.
The problems of cell transfection in a vertebrate animal was that the cell transfection reagents or procedures (except for adenoviruses and microinjection of single cells) would introduce the gene of interest into a wide variety of cells. There were unique problems, whether the genes were viral, bacterial, or of the same or other species.
If someone was interested in restoring in vivo production of human insulin to type one diabetics, that was entirely possible, at least transiently. The problem was that the regulatory mechanisms for starting and stopping insulin production were cell-specific and not in the insulin gene. So if you introduced the human insulin gene into a wide variety of cell types due to the indiscriminate nature of most cell transfection reagents and methods, those cells would happily churn out insulin. But there would be nothing to regulate it. Overproduction of insulin would rapidly lead to extreme hypoglycemia, unconsciousness, and then death.
And the cellular production of virtually all proteins is regulated in a tissue-specific way. It doesn’t do much good to produce a normal protein someone with a genetic disease lacks if you can’t control where it’s produced and its quantity.
As far as viral and bacterial proteins are concerned, it’s trivial to get cells to produce them. But since both those cells and the innate immune system can detect the presence of viral or bacterial proteins, producing them in vivo will ALWAYS recruit the innate immune system to launch innate immune inflammatory attacks on those cells. Why? Because those cells, detecting the presence of pathogenic mRNA and pathogenic protein, signal that they have been invaded by pathogens, are in replication mode, and have to be killed.
This is the inevitable result of the primary mechanism of action of ALL viral mRNA products. And when you have that occurring in cells across multiple organ systems simultaneously, the innate immune system reacts appropriately as though responding to a broadly disseminated, massive viral infection and with predictable results.
ALL this was known long before any EUA for these products were granted. Any possible effects of any non-payload ingredients the cell transfection agents use are irrelevant compared to the intended effects of the products themselves.
So what if somewhere downstream you’re able to make antibodies and T cells against the viral proteins. Big deal. You can do that with viral protein vaccines. But viral protein vaccines don’t invade cells like viruses and hijack protein production like viruses and cause the cells to recruit innate immune inflammatory attacks like viruses.
But ALL viral mRNA products do.
And the point of viral protein vaccines was to skip the infection part and just do the adaptive immune part. You know, protection without infection.
ALL the viral mRNA products work by infecting healthy cells with viral genes. That’s disease. They triggering an innate immune response to kill those cells. That’s a disease response.
And, because of the products’ indiscriminate nature, they’re initiating this everywhere relatively speaking all at once. And the innate immune response is proportional and, depending of how much inflammatory damage and to which organs, will be debilitating or deadly.
THAT is the inherent nature and outcome of the viral mRNA products.
Cell transfection reagents? Great. In their proper place in the lab. In the body? Not so great, unless, of course, you’re aiming to do harm, and there are MANY ways that could be used to cause harm.
Now that there are worldwide production, distribution, delivery, and regulatory systems in place, imagine what would happen if some bad actor introduced the human insulin gene into the mix or the gene of a protein that would bind irreversibly to receptors at neuromuscular junctions.
If it’s not a viral or a bacterial gene, it would never be noticed by the cells or the innate immune system and the first you’d notice anything would be as you were slipping into an insulin coma or becoming paralyzed.
OMG! Some technologies don’t need to be pursued! Scientists need to recognize when they should abandon their research & development. Unless they’re psychopaths wishing to do harm.
Key point - “unless they’re psychopaths…”. Unfortunately that is what we are dealing with, that and too many medical professionals that don’t have the courage to stand up and shout that this is deadly poison.
Yes trump and bobbi are trying to distract us now with other subjects. Chem trails, food, chronic diseases that are so prevalent now, due To the mrna shots. But never mentioning the shots as the cause.
I have made myself clear, I will not go away. I know you have seen in my stacks and interviews that I will not be silenced or go away. I cant. and POTUS Trump must stand up to the failure of OWS and the mRNA vaccines. Kennedy Jr. has not changed his position, he cant for his legacy and name is built on this. Nothing must silence someone like Kennedy in this. Nothing. I think he knows that and yes, there is silence I myself have noted but he will come out soon...it will be interesting how the system takes him then. he actually has the upper hand.
Consciousness Within ourselves creates the Ripple in The Pond of Emotions which creates the Environment of The Quantum Field of The Planet!!! We R Billions The Elite Thousands or hundreds!!! Me/We there is No Separation!!! 💓🎶👍
Trump is losing votes with the Death Vax approval! We the People are not ignorant! It is making him a part of the massive destruction it has caused! Thank You RFK and Dr Alexander for your constant and unwavering devotion to getting the truth out from the beginning❣️
but today they understand, many, that they were screwed lied to by all involved. dont you think it will impact how they vote? what happens if Kamala throws a hail mary if she is down....? and blames it all on Trump, drops it on him?
Trump is also losing conservative votes due to his announcement that he’ll mandate insurance coverage for IVF procedures. It sounds like a good thing, but many more embryos are destroyed than survive, in the process. Pro life supporters don’t go for that. Why is he fucking with his loyal base right now? Is he stupid? I can’t believe he even went there. I know a lot of people who aren’t planning to vote now. He is pissing off his base supporters. Who the hell is advising him? He needs to apologize for OWS & his mistaken stance on vaccines, & stand with his pro life base. Stop the mass poisoning & there won’t be a need for IVF procedures to have a baby.
we have said his campaign managers are subverting him...I TOO have issues with that position. we are allowed to. we have questions on this...it is a very vexing issue for women too...I can only imagine the pain and suffering and mental torment...
Not voting for Trump helps Harris. Why are the lot of people you know planning to help Harris? What's so good about Harris that the people you will not vote against her?
nothing is good about HARRIS, zero. I dont want anyone bailing on Trump for Harris...zero...people are upset and bitching but they go to stay firm but Trump has to give some sugar, no? something to hold to until after the next 8 weeks?
as you read, you can see my goal was not to be complicated, no fancy biochemistry, just my 50,000 foot view on this mRNA technology and what I think is needed now. to drive debate and in my words, no one wrote this for me...there has been a move now among some substack writers to have people write their work and they pay them to. it is becoming clear who writes what...even in substack it is becoming a quasi-fraud. again, the public always loses. we have commentors on stack who we do not know real identities and some writers who do not write their own work. ugh
Frankly, if someone says the "right" thing based on solid research, I don't care who posts it. We need all the help we can get to get people to pay attention because we need all the people we can get to expose and share the truth. PS: Although I really like the words YOU wrote, especially when you're angry - lol
thanks, hugs...today dealing with some family health but am tending to an interview later and stack and reading etc. but boy am I angry...of the lies
I agree with you but they're not going to stop this vaccine or any others they're working on because it's the depopulation plan from the WEF. Next step is to force vaccination. Washington state wrote and passed laws recently to do just that using police and military if necessary in a future
pandemic (actually plannedemic). Dr Ana Maria Mihalcia's recent substack has all of the Washington state law. She lives in Washington state. No doubt all blue states will follow Washington state. God save us.
I agree here too big time...some form of depopulation...sickening...and we live the ugly lie of it all
https://www.thegatewaypundit.com/2024/09/world-economic-forum-finally-tells-truth-about-covid/
I find it strange that you keep calling Trump the president of the United States when he is not and he has no intention of stopping any va€€ines as he is part of the system (WEF)
Also the mrna va€€ines are doing exactly as intended except maybe it's not doing as much harm as they would like
I present to you personally an honest fellow quite astute with the initials JR who I think you may know. He is my reference, we live not far apart. He knows all about my existence. Just ask him anytime.
I think this is where Kennedy Jr. will make his mark, he has too, he grew due to this and it has only gotten worse...so I am confident.
It’s more than 40 year old cell transfection reagents in a seriously off-label use to infect healthy cells with viral genes.
That’s ALL it is.
How do I know?
Because I regularly used those same cell transfection reagents starting back in the 1990s in my labs in my doctoral and post-doc research.
It was a completely trivial process even back then. The only difference are that these guys are using it in a way that no IRB in any university would have approved.
this is the key, thank you for sharing this critical information Gregorio, we are not experts in this and it is important folk like you share your expertise.
And thank you, Paul. Also, given how critical small numbers of progenitor cells are in development (but also in adult stem cell populations), a product capable of whacking these cells is capable of deranging downstream developmental pathways. Two obvious outcomes to expect would be an increase in miscarriages and immune system and blood problems (most of which cells come from the hematopoietic stem cell population).
See my reply to Sue Palmer
Agree.
https://forbiddennews.substack.com/p/stories-from-aurora-colorado-you?
this is very terrible and the point is if as reported that the govn will not handle it, then the people have to handle their business.
I hope if Poilievre becomes PM will do something about these illegals.
we hope...we hope anybody can do something....
Agree.
Hi Luc. Here's another link about Arura Colorado and the gangs there.
Enjoy....
https://youtu.be/cgaC3-BmE1U?si=KU6n1gbSRmLN0o8P
Indeed, terrible.
Sad to say we can't take the law into our own hands.
Not now anyways.
Nice shot,Luc. These things used to just happen in government housing projects.
Now that it's happening in wealthier people's complexies,folks may take notice.
You are correct Doc. My words to the damned CYSTem is flock off because I will never accept the D&D jab. (death and destruction) They can shove it up their ample asses.
"All prior research has shown the mRNA-LNP platform to be toxic, poisonous and deadly. "
But extremely profitable.
kaboom...thats the key, profitable
we are expendable to these beasts
If mRNA tech is good enough for JD Vance maybe it's not a bad thing?
BUSINESS Battelle, investors including J.D. Vance, launch gene therapy startup, AmplifyBio
https://www.dispatch.com/story/business/2021/05/05/battelle-investors-including-j-d-vance-launch-gene-therapy-startup/4935970001/
AmplifyBio and RNAV8 Bio Announce Strategic Partnership to Support mRNA Therapeutic Developers from Sequence Design to GMP Manufacture
https://www.amplify-bio.com/amplifybio-and-rnav8-bio-announce-strategic-partnership-to-support-mrna-therapeutic-developers-from-sequence-design-to-gmp-manufacture/
this is very troubling and I have been reading...so how do we handle this? to table it means he hit Vance...we are in such a shit situation for we cant let Harris et al near the chair but Vance got to explain this...is it just about money to these people?
The LAST thing The USA needs is anymore artificial bullshit form BIG HARMA.
boom!
There is no safety with mRNA LNP technology. It’s bio weapon technology that they intend to keep using. Just ask JD Vance. And all the other players salivating over their future profits. They don’t give two shits about our safety.
very correct, 100%...it was never safe and will never be safe
Agree with many of your points. However, Robert Malone, who created the mRNA technology, has not been silent. He warned his colleagues of the dangers and problems with it but they ignored him and went forward. He has always been outspoken about the dangers of that technology.
thanks for being here. hugs, respect....there is a reason why Malone stayed silent for so long...he did not warn anyone, he was silent UNTIL he could be no more...he shilled the shots...the trail is there. but note I state 'oaths'...proper courts...it is there that the truth emerges. not congress or no dog and pony bullcrap we have been subjected to. then tell your friend Robert et al. to interview with folk like me, McCullough et al. Couey, Yeadon...he wont because he cannot defend his actions. sorry that you believe that crap he sold you. I have no issue with him personally, its just that he is a fraud and took people's money based on lies and his work killed people. if Bourla, Fauci, Birx, Bancel et al. are to be investigated, he must be too. not because you 'like' what he sold means we go with that. no...he is as culpable and proper hearings can decide the extent. and if there is to be consequences...he moves like Biden and Kamala, reads from phones and teleprompters for there are legal issues involved in his words and also, he wont talk to the right people. for now.
I did not realize he was quiet for so long. Only heard him speaking out several times. Thank you.
Yes Sue he did - BUT he only spoke out when it became obvious it was harmful. He in fact, had little to do with the whole project, but tried to claim fame when everyone (except myself, Dr Alexander et Al) thought it was a miracle cure. As soon as the VAERS reports began stacking up, that snake in the grass jumped ship and pretended to be a whistle blower and no longer claimed he “invented” mRNA technology. Because his colleagues had long since outed him as a fraudster anyway!
Many “X”ers and sub-stackers have labeled him “controlled opposition” but just personally, I don’t think he’s that clever m, he is just an everyday coward running from the part he played in ruining millions of lives!
Sorry but he belongs up on the g@ll0ws right beside Fauci!!!!
I agree...but we always have proper hearings first. but he is a con artist...and how you stated it is exactly how it has played out. he wanted money on upside selling it and on downside when the shit hit the fan
many on the COVID grift train are same and did same
Does Malone write his own stuff? Some substacks are probably written by AI, just like scientific journal articles. It would be interesting to know what JD Vance's perspective is on Malone, given AmplifyBio's role in promoting mRNA therapeutics.
He lost me with that talk with children in Hawaii.
Malone used the EXISTING procedures and reagents of cell transfection to develop a particular in vivo use in an attempt to counteract the effects of mutated proteins in a transient fashion, either to outcompete with normal gene products the products of a defective protein that resulted in a disease state or to silence that expression of the defective gene, either of which, depending on the condition, had at least the theoretical possibility of restoring at least some function and reducing the disease phenotype.
He was not to cell transfection what Kerry Mullis was to PCR.
The cell transfection reagents began as attempts to introduce therapeutic agents directly into the cells of diseased tissue. This was a noble attempt. Why? Because while chemotherapy works, it works by killing cancer cells at a more rapid rate than non-cancerous cells--but it still whacks normal cells.
The hope was to design cancer cell-specific reagents that would target ONLY cancer cells, perhaps targeting a cell surface receptor or other cell surface protein unique to cancer cells. This way a very small amount of the therapeutic agent could be targeted only to where it was needed, sparing healthy cells and also reducing the amounts needed of very expensive drugs.
The problem? At that time, at least, they couldn’t get specific enough. But someone else figured out that they were great vehicles for delivering exogenous genes into cell without killing them, expressing exogenous proteins in those cells, and being able to study the expression and behavior of those proteins in the context of a living cell. And, so, the era of modern molecular biology was born.
With the extreme ease via PCR and the use of a huge variety of restriction enzymes (acquired from bacteria that used them to chop up the DNA or RNA of invading viruses), it was possible to identify by the use of point mutations as well as insertion or deletion mutations or chimeric mutations, the functional regions of particular genes. But the way of seeing the effects of those deliberate mutations was to see how those proteins behaved inside of cells.
And those cells used were any of a variety of immortal cell lines. The benefit of using them was that they had been fully characterized and that they were monocultures of cells that had no innate or adaptive immune system activity to screw things up.
The problems of cell transfection in a vertebrate animal was that the cell transfection reagents or procedures (except for adenoviruses and microinjection of single cells) would introduce the gene of interest into a wide variety of cells. There were unique problems, whether the genes were viral, bacterial, or of the same or other species.
If someone was interested in restoring in vivo production of human insulin to type one diabetics, that was entirely possible, at least transiently. The problem was that the regulatory mechanisms for starting and stopping insulin production were cell-specific and not in the insulin gene. So if you introduced the human insulin gene into a wide variety of cell types due to the indiscriminate nature of most cell transfection reagents and methods, those cells would happily churn out insulin. But there would be nothing to regulate it. Overproduction of insulin would rapidly lead to extreme hypoglycemia, unconsciousness, and then death.
And the cellular production of virtually all proteins is regulated in a tissue-specific way. It doesn’t do much good to produce a normal protein someone with a genetic disease lacks if you can’t control where it’s produced and its quantity.
As far as viral and bacterial proteins are concerned, it’s trivial to get cells to produce them. But since both those cells and the innate immune system can detect the presence of viral or bacterial proteins, producing them in vivo will ALWAYS recruit the innate immune system to launch innate immune inflammatory attacks on those cells. Why? Because those cells, detecting the presence of pathogenic mRNA and pathogenic protein, signal that they have been invaded by pathogens, are in replication mode, and have to be killed.
This is the inevitable result of the primary mechanism of action of ALL viral mRNA products. And when you have that occurring in cells across multiple organ systems simultaneously, the innate immune system reacts appropriately as though responding to a broadly disseminated, massive viral infection and with predictable results.
ALL this was known long before any EUA for these products were granted. Any possible effects of any non-payload ingredients the cell transfection agents use are irrelevant compared to the intended effects of the products themselves.
So what if somewhere downstream you’re able to make antibodies and T cells against the viral proteins. Big deal. You can do that with viral protein vaccines. But viral protein vaccines don’t invade cells like viruses and hijack protein production like viruses and cause the cells to recruit innate immune inflammatory attacks like viruses.
But ALL viral mRNA products do.
And the point of viral protein vaccines was to skip the infection part and just do the adaptive immune part. You know, protection without infection.
ALL the viral mRNA products work by infecting healthy cells with viral genes. That’s disease. They triggering an innate immune response to kill those cells. That’s a disease response.
And, because of the products’ indiscriminate nature, they’re initiating this everywhere relatively speaking all at once. And the innate immune response is proportional and, depending of how much inflammatory damage and to which organs, will be debilitating or deadly.
THAT is the inherent nature and outcome of the viral mRNA products.
Cell transfection reagents? Great. In their proper place in the lab. In the body? Not so great, unless, of course, you’re aiming to do harm, and there are MANY ways that could be used to cause harm.
Now that there are worldwide production, distribution, delivery, and regulatory systems in place, imagine what would happen if some bad actor introduced the human insulin gene into the mix or the gene of a protein that would bind irreversibly to receptors at neuromuscular junctions.
If it’s not a viral or a bacterial gene, it would never be noticed by the cells or the innate immune system and the first you’d notice anything would be as you were slipping into an insulin coma or becoming paralyzed.
OMG! Some technologies don’t need to be pursued! Scientists need to recognize when they should abandon their research & development. Unless they’re psychopaths wishing to do harm.
Key point - “unless they’re psychopaths…”. Unfortunately that is what we are dealing with, that and too many medical professionals that don’t have the courage to stand up and shout that this is deadly poison.
No, that research is absolutely essential. Just because some whack applications are bad is no reason to get rid of the basic tools.
Fire: good.
Arsonists: bad.
Tylenol: good.
Tylenol laced with cyanide: bad.
Steak knives: good.
Murder by steak knife: bad.
Panel vans: good.
Panel van used by whack job Muslim to run down people on a pedestrian path: bad.
None of those bad outcomes justifies getting rid of the primary use.
I respectfully disagree with regards to AI & mRNA LNP. These are evil & will be & are being deployed as such.
Ongoing research on mRNA therapeutic vaccines is essential but they are not yet ready for prime time?
So:
Cell transfection of exogenous genes in cell culture: Good.
Cell transfection in vivo of viral genes mischaracterized as a vaccine: Bad.
No, they are inherently bad for the reasons I stated. They are nothing more than indiscriminate single gene artificial viruses.
I was referring to molecular biological research in general using the techniques of cell transfection to express exogenous genes in cell culture.
I don't know what to make of this: These weren't therapeutic vaccines, just the regular clot shot.
Spontaneous tumor regression following COVID-19 vaccination
https://jitc.bmj.com/content/10/3/e004371
Spontaneous regression of advanced hepatocellular carcinoma following COVID-19 infection and vaccination: a case report and review of the literature
jgo-15-04-1933.pdf
B.S. Doctors need to STOP playing God.
Only in very elliptical ways.
Yes trump and bobbi are trying to distract us now with other subjects. Chem trails, food, chronic diseases that are so prevalent now, due To the mrna shots. But never mentioning the shots as the cause.
I have made myself clear, I will not go away. I know you have seen in my stacks and interviews that I will not be silenced or go away. I cant. and POTUS Trump must stand up to the failure of OWS and the mRNA vaccines. Kennedy Jr. has not changed his position, he cant for his legacy and name is built on this. Nothing must silence someone like Kennedy in this. Nothing. I think he knows that and yes, there is silence I myself have noted but he will come out soon...it will be interesting how the system takes him then. he actually has the upper hand.
Indeed
So after so many deaths from the poison vaccine the WEF now admits it was a test. Those of us that didn't fall for it will be targets for sure. See this link: https://www.thegatewaypundit.com/2024/09/world-economic-forum-finally-tells-truth-about-covid/
The continued use of LNP is to ensure that the Human peoples become infertile.
Humanity will become dependent upon artificial methods for reproduction [at the behest of Satan].
FRIENDS; BIG PHARMA GAVE 1.5 MILLION PEOPLE CANCER THROUGH THE SV40 IN THE POLIO VACCINE. https://www.youtube.com/watch?v=TcbuqQd57rY
Consciousness Within ourselves creates the Ripple in The Pond of Emotions which creates the Environment of The Quantum Field of The Planet!!! We R Billions The Elite Thousands or hundreds!!! Me/We there is No Separation!!! 💓🎶👍
great sharing
Trump is losing votes with the Death Vax approval! We the People are not ignorant! It is making him a part of the massive destruction it has caused! Thank You RFK and Dr Alexander for your constant and unwavering devotion to getting the truth out from the beginning❣️
Why would it be losing him approval? 81% of Americans lined up for the shot. Nobody put a gun to their heads.
but today they understand, many, that they were screwed lied to by all involved. dont you think it will impact how they vote? what happens if Kamala throws a hail mary if she is down....? and blames it all on Trump, drops it on him?
Trump is also losing conservative votes due to his announcement that he’ll mandate insurance coverage for IVF procedures. It sounds like a good thing, but many more embryos are destroyed than survive, in the process. Pro life supporters don’t go for that. Why is he fucking with his loyal base right now? Is he stupid? I can’t believe he even went there. I know a lot of people who aren’t planning to vote now. He is pissing off his base supporters. Who the hell is advising him? He needs to apologize for OWS & his mistaken stance on vaccines, & stand with his pro life base. Stop the mass poisoning & there won’t be a need for IVF procedures to have a baby.
we have said his campaign managers are subverting him...I TOO have issues with that position. we are allowed to. we have questions on this...it is a very vexing issue for women too...I can only imagine the pain and suffering and mental torment...
Not voting for Trump helps Harris. Why are the lot of people you know planning to help Harris? What's so good about Harris that the people you will not vote against her?
nothing is good about HARRIS, zero. I dont want anyone bailing on Trump for Harris...zero...people are upset and bitching but they go to stay firm but Trump has to give some sugar, no? something to hold to until after the next 8 weeks?
So agree but what indication do you have that DJT will “get it” this time if he survives and manages to get into the White House?