What will be done? I want to see those responsible indicted and prosecuted. Pfizer murdered my sweet husband and these criminals need to pay. I’m waiting and watching. I’m tired of just talk. 👁️👁️
Exactly. I live without my sweet husband that Pfizer murdered without recourse. I inform everyone in my life to never listen again and to take spike protein detox if they got jabbed. Some listen, most don’t cause they are not suffering, yet.
People are like cult members. They know something bad is happening, but they don't know who is causing it, and they don't know what to do. Time will open their eyes, and unfortunately, I know after FIVE YEARS of trying to warn people and losing nearly ALL my friends, people have to be DE-PROGRAMMED, like cult members, because they are victims of terrorism without knowing who is doing the terror.
Welcome to my world! Five years now, and other issues before that! It's time to put the Tyranny back in the sewer where it belongs before it rips our planet apart. I've been hoping people would start "catching on," and-- they ARE. It's GOOD!
There is no such thing as a "covid-riddled" anything. There is no evidence of any virus, EVER. There is only people telling us there are viruses. What is far more likely is that your loved ones and friends have been harmed and killed by the "cure"-- the vaccine. It is shown, first by a Spanish laboratory called "La Quinta Columna," that at least some of those vials of "vaccine" were loaded with hard-core toxins, like mercury, lots of aluminum, graphene oxide... and more. ALL injections are now shown to be the wrong thing to do, and ALL vaccines contain toxins! Just leave it and go to a Naturopath! The symptoms of most illnesses are Nature's way of DETOXING the stuff causing the troubles. We're only now beginning to see the amazingly beautiful system our bodies have been endowed with, BY OUR CREATOR. xo
The SV40 virus can be the culprit if people have gene mutations and took the Pfizer or Moderna jabs. Kevin McKernan a gene expert in Canada talks about it being a death sentence. You can watch his videos about it. The PLANDEMIC OF FEAR INDUCED MANDATED POISON JABS. 💉💉💉💉💉
Well, I can’t make anyone believe or disbelieve anything, but I am completely convinced that viruses do not exist. Period. As for jabs, I wouldn’t touch one with a barge pole. If the Nasties make it to mandating death jabs, you can bet that will be the time of insurrection, if it hasn’t started already.
I think I may have answered this already, but it’s here in my “feed” again… ;)
There are no VIRUSES. It started out as a mistake, and became a VAST money-maker with the vaccines, so it hasn’t quite gone away… Don’t worry, NO virus has EVER been isolated!
I never feared anything covid. All one big scam. It still surprises me how much it affected so many with fear. They don’t get what was done to them. More will get sick, more will pass.
Try not to let it take over your brain... We are going to need level-headed, CALM responses to this in order to bring this down... They've been planning this for DECADES, and they are PREPARED, and we are not.
😊it’s been hard. When someone comes to your door and shoots to kill, you can indict and prosecute. But when Pfizer and all cohorts murdered my sweet husband, I just can’t get a grip on it. The responsible parties lists are enormous. I see nothing happening that would show me anyone cares. Hopefully RFK Jr. cares. As time goes on more victims will be evident, maybe then when it’s their loved one, caring will begin. Thanks for your notes.
And I suggest you think of things this say: Anybody who is in power politically is likely part of the Nastiness, or they’re unwitting dupes. This is much much bigger than a fake virus.
And the PCR is NOT A TEST, it doesn't diagnose anything, and even our own folks who are the Resistance use this phrase, "PCR Test," which enrages me because it is used to LIE to people so they keep getting the JAB!!!!! Makes me so furious.
Why are Gates and Fauchi and their cohorts not in jail? The evidence is overwhelming of their crimes against humanity. The pardons,the fool Obiden auto signed, aren’t worth the paper they are written on. Why are these murderers still free to continue their obsession to kill us all off ??? Why are the poison jabs still on the market ??? Where has all the sanity gone? I was one of the lucky ones who didn’t take the bait but I have many friends who did get the jab. Their illnesses run the gamut from senility, disabilities to blood cancers. When is this madness going to stop and those responsible held accountable for their diabolical actions?
Because so far, those who could do what's right ARE IN ON THE THING. I'm telling y'all, this has been planned for DECADES. They will sacrifice those who are shown to be evil, when they need to. Because the people behind all this Don't Mind Killing.
ALL the Five Eyes Govt's and many of Europe's leadership ARE IN ON THIS.
It's SO much bigger than "covid." It's a globalist coup and a global genocide. Yes, it sounds insane... IT IS INSANE. But there it is. I've been onto this for FIVE YEARS. Slowly, I've learned SO MUCH and none of it, well, hardly any of it, is GOOD. It does turn out, tho, that our bodies are a miraculous gift from our Creator, and getting a "vaccine" is never, ever, a good thing.
Problem is no truth in mRNA or DNA found in vials. Graphene Oxide is found in the vials. Micro Raman technology finds no organic material. We present here our research on the presence of graphene in covid vaccines. We have carried out a random screening of graphene-like nanoparticles visible at the optical microscopy in seven random samples of vials from four different trademarks, coupling images with their spectral signatures of RAMAN vibration. By this technique, called micro-RAMAN, we have been able to determine the presence of graphene in some of these samples, after screening more than 110 objects selected for their graphene-like appearance under optical microscopy. Out of them, a group of 28 objects have been selected, due to the compatibility of both images and spectra with the presence of graphene derivatives, based on the correspondence of these signals with those obtained from standards and scientific literature. The identification of graphene oxide structures can be regarded as conclusive in 8 of them, due to the high spectral correlation with the standard. In the remaining 20 objects, images coupled with Raman signals show a very high level of compatibility with undetermined graphene structures, however different than the standard used here. This research remains open and is made available to scientific community for discussion. We make a call for independent researchers, with no conflict of interest or coaction from any institution to make wider counter-analysis of these products to achieve a more detailed knowledge of the composition and potential health risk of these experimental drugs, reminding that graphene materials have a potential toxicity on human beings and its presence has not been declared in any emergency use authorization. We leave a link to download this report at the end of this video. https://www.researchgate.net/publication/355979001_DETECTION_OF_GRAPHENE_IN_COVID19_VACCINES
And, there's this from yesterday's "Lioness of Judah" substack........
That's pretty harsh, pegging them as GMO's, but it brings a vital question to play.
The numbers reflecting a systemic "failure to reproduce" in vaxxed people is becoming alarmingly clear. Simply, not only this generation, but future gen's were also plagued. The miscarriages, stillborns, loss of menstrual cycles, etc. all point to significant reproduction issues.
Will purebloods become the breeding stock? Would you want your pureblood son or daughter to risk your future grandchildren with a vaxxed partner?
What the fuck are "purebloods"? Are you living in Harry Potter world? lol
And yeah, Christians, and EVERYONE ELSE that is a Human Being... getcha head on straight, my friend, this is not the time to be hating on your fellow Humans. We are an ENDANGERED SPECIES right now. ALL people who believe in LOVE are worthy.
Well, you’re telling me something. Are you going to show me the PROOF of what you’re telling me? You may be right, but there are discussions about DNA, too. We’ve been told SO many lies, I don’t just accept something like that anymore, and besides, I’ve heard this already and I don’t trust it. :)
And I’m not a “mr.” either. But I sound like one, people tell me. Woof!
Hello, Ms. Herder (if this is incorrect, sorry, I only have two choices...)
I share your bewilderment, and the constant nagging desire to question and challenge everything, particularly authority. We don't trust anybody to tell us the complete truth anymore.
The intention of my post was more to post thought-provoking questions that will have to be acknowledged at some time, not to stir up hate and discontent.
My oldest grandson is posing situations right now that could have him enlisting in the Air Force after H/S graduation and marriage to a vaxxed young woman. I don't know the lucky lady, but I would bet she's a truly wonderful person with high morals. I hope you can see where this circumstance evolved into the post yesterday, and the true intentions.
These are difficult times, and this would be a very difficult topic in any environment. We were never equipped with tools to combat a treasonous gubmint, except the small arms of war. This is uncharted territory.
It’s very disheartening to see things like this on other pages written with what seems either an almost a flagrant disregard for the immunological basis of what’s going on or a conscious attempt at sensationalism.
And given the actual primary mechanism of action common to ALL the viral mRNA products that I have described in detail for years, such sensationalism is only gilding the lily.
How do I know what exactly what the primary mechanism of action is?
Because I have used it more times than I can count since the late 1990s in my doctoral research in molecular neurobiology and then in my post-doctoral fellowship on a cardiology training grant in a neurobio/pharm/phys lab.
And it’s THIS stuff that has to be understood to be able to sort through all the weird stories that have flooded the internet since late 2020.
The real mystery, yet to be fully explained, was why both principal groups of critics of those products were as mum about it as the companies producing the products were.
There were two groups of critics, 1. The sensationalist “snake venom, 5G self-assembling nanobots, aborted fetuses, HIV, etc,” and 2. The more mainstream science-appearing guys appearing in groups to talk to Ron Johnson on Capitol Hill.
The first I believe were probably funded by the viral mRNA companies themselves to make all critics of the products look like completely hysterical morons.
The second is much more problematic for two reasons:
1. They talked about everything BUT the primary mechanism of action common to all those products, and
2. Any of them that had any real research experience in molecular biology knew exactly what it was before any of those companies announced in the latter part of 2020 that they would be using “viral mRNA.”
Here is what someone like Robt Malone would have known: in molecular biology the four most stupendous discoveries/innovations and upon which virtually all research in molecular biology depends, were (not in any particular order):
1. PCR,
2. Simple, quick, easy to use, and reliable Sanger DNA sequencing,
When I wanted to figure out what was going on in cell-cell adhesion due to the developmentally-driven expression of a certain class of neural cell adhesion molecules responsible for neural pathfinding, neuron bundling, and nerve insertion into the target tissue, I needed a way to examine the roles carried out by the different domains of the cell adhesion molecule: the extracellular domain that bound in a homophilic and irreversible fashion to other such molecules on other cells, the transmembrane domain that kept in place, and the cytoplasmic domain that, eventually, would bind to cytoskeletal proteins and result in signal transduction, driving the developmental process. Some of the questions were:
1. What are the minimum conditions for cell-cell adhesion?
2. What are the minimum conditions for the recruitment of cytoskeletal proteins to the cytoplasmic domain of this class of cell adhesion molecule,
3. What is the order in which these events take place, especially the events downstream of cell-cell adhesion that recruit first one cytoskeletal protein to the cytoplasmic domain and then, following that, other cytoskeletal proteins to bind to them in order to activate gene expression in those cells in a developmentally favored way?
To do that, I would need:
A. to be able to identify the parts of the gene responsible for the different domains in the protein. It was PCR and DNA sequencing that made this possible.
B. to be able to chop those different domains apart at will. It was restriction enzymes that cut apart DNA at specific locations that made this possible.
C. to be able to assemble the DNA for the cytoplasmic/transmembrane domains with the DNA for the green fluorescent protein so I can track in real time where those extra cellular domains are in the membrane. It was PCR and sequencing that enabled me to see if I had successfully gotten the different fragments ligated in the proper order and correct orientation.
D. to be able to assemble the DNA of an extracellular domain with no binding activity from some other protein with the cytoplasmic domain of the cell adhesion molecule so I could selectively control, by the use of primary antibodies specific to that extracellular domain and secondary antibodies that bind to the primary, the aggregation of the cytoplasmic domains of the cell adhesion molecules in the absence of the cell adhesion molecule’s extra cellular domain. If this resulted in the selective binding of the cytoskeletal proteins, then it would mean that the cytoskeletal binding was controlled only by the propinquity of the cytoplasmic domains and that the role of the extracellular domain binding to others on another cell in contact served to concentrate them enough that the two binding domains on the cytoskeletal protein can bind to two different cytoplasmic domain of the cell adhesion molecule. It was PCR and sequencing that enabled me to see if I had successfully gotten the different fragments ligated in the proper order and correct orientation.
E. to be able to see any of that happening in living cells, I had to have a way of getting my gene constructs inside identical cells of a stable, well-characterized, immortal cell line. It was the use of either of two cell transfection reagents that enabled me to do that. One type was like that used by Pfizer. The other types were like those used by Moderna and Johnson&Johnson. I knew about but had no reason to use the adenovirus method used by AstraZeneca.
Everything I described above are just basic molecular biology techniques.
In the work I and hundreds of thousands of other molecular biologists did, we didn’t have to worry about the effects of innate or adaptive immune response for one simple reason: monocultures of immortal cells lines don’t HAVE innate or adaptive immune systems.
We also didn’t have to worry about those cell transfection reagents getting our gene constructs into any cell they bumped into. For us, it was the more, the merrier.
The viral mRNA companies did nothing but take decades-old reagents and techniques for dangerous off-label uses to introduce viral genes into healthy cells. And since those products carrying the viral genes would enter into any cells in any organs they bumped into, this meant those viral genes would be used in all those cells to produce in an uncontrolled manner many copies of a full length, physiologically-useless, but biologically-active viral protein.
And what would be the inevitable consequences of that?
Well, as Pfizer described it, “Our product only gives your body the information it needs to build immunity.”
But what they did NOT say was that the product-compromised cells, because of built-in internal sensors, would detect the simultaneous presence of viral mRNA and viral protein and then signal the innate immune system to launch innate immune inflammatory attacks to kill those cells.
Why does that happen?
Because the simultaneous detection of viral mRNA and viral protein is the minimum necessary condition to indicate viral infection that is in the replication phase. This is a disease process.
But the intensity of the innate immune system is a hierarchy of responses. The more signaling, the greater the response. The greater the number of organ systems involved, the greater the response.
Now, all that is happening before any member of the innate immune system comes into physical contact with a single viral protein. It’s happening before the adaptive immune system is ever involved.
Large enough innate immune inflammatory attacks just at that initial level can kill.
In an actual viral infection, that’s going on from the earliest time points, but it’s happening locally and a restricted manner.
And when a few viruses escape the innate immune inflammatory attacks, they can be physically detected by the innate immune system. And if you have an existing adaptive immune response to some of those proteins, they will start being tagged by antibodies and attacked by T cells. But still, it’s going on at the earliest timepoints and in restricted ways.
But with the viral mRNA products, everything starts out at a greatly elevated level of response. First with the innate immune inflammatory attacks on product-compromised cells in multiple organ systems.
Then there’s the appearance everywhere of the viral proteins.
Some may think, “Yeah, but they’re not viruses.”
That’s irrelevant because the innate and adaptive immune systems do not detect viruses or bacteria. They detect only viral and bacterial proteins (and some pathogen-specific glycosylation).
The adaptive immune system does NOT make specific antibodies and T cells against viruses or bacteria. It makes antibodies and T cells that are specific only for epitopes on individual viral and bacterial proteins.
And this is why injecting someone with a bunch of viral proteins, especially a broad variety of viral proteins, will create the same kind of adaptive immune response that exposure to an actual virus will--except without getting infected.
But in the case of the viral mRNA products, the big flood of viral proteins released following innate immune inflammatory attacks will be detected as viruses by the innate immune system as it comes into contact with them. And the greater the number of contacts, the greater the volume of those contacts, and the greater the number of organ systems involved, the greater the level of innate immune response--on TOP of that initial provocation at the cellular level.
And everything I described above in this part is just basic immunology. It’s something that many people employed by all those companies should have understood.
I understood it.
And even Robt Malone understood it. He said, “No one should be getting viral genes as a vaccine, especially not the way they’re doing it.”
But for years that very guarded and tepid response was the closest that anyone in that second group of critics came to describing the primary mechanism of action common to all those products.
And it was years until anyone was coming anywhere close to what I had been describing for years.
Now, based on all the above, one will have all he needs to understand that the viral mRNA products do not “cause” cancer.
And, in a related story, the viral mRNA does NOT “awaken” the “world’s deadliest virus.”
Here is what is actually going on.
In addition to an innate immune system, the human body, like all vertebrates also has an adaptive immune system.
The only time anyone really notices the innate immune system is either after getting a cut or scratch or scrape when you get a little inflammation around the wound or when you’re “coming down” with something.
In the latter case you are NOT feeling the effects of whatever you’re “coming down” with.
You are feeling the effects of your innate immune system gearing up to fight it.
Sniffles, coughing, sore throat, aches and pains, a fever, crankiness, ALL that is caused by your innate immune system.
You know how we know that?
You know the expression “snot-nosed kid”? You know why most kids, by the time they’re older children and teens, are no longer snot-nosed kids? It’s because through their repeated encounters with any of almost 200 common cold viruses, they have been gradually building up a general immunity against developing serious clinical cases.
They’re still getting infected. No one EVER stops getting infected. But the greater your repertoire of antibodies and T cells, the less work your innate immune system has to do to put it down.
And since many families of common cold viruses have varying numbers of viral proteins in common and since neither the innate nor adaptive immune systems recognizes viruses or bacteria, only viral or bacterial proteins, then each type of cold you get will boost your response to proteins your adaptive immune system already recognizes and your adaptive immune system will design new antibodies and T cells against the balance of proteins it’s encountering for the first time.
The more times you get infected, the greater your adaptive immune repertoire and the less work your innate immune system has to do. The less your innate immune system has to do, the less you notice it.
So when you don’t feel sick, it’s not that your innate immune system is not doing anything, it just doesn’t have to do as much.
But all the while, it’s constantly encountering and destroying stuff every day. There are certain viruses that keep replicating at a very low rate for a variety of reasons, but since their number is kept low by both the innate and adaptive immune system, you never notice it.
Why?
Because your adaptive immune system doesn’t get spun up enough for you to feel it.
So in the absence of some new virus, your innate and adaptive immune systems are maintaining a status quo whereby things are kept in check.
Doing that, whether it’s spotting and taking out neoplasms or foreign bacteria or viruses or holding stuff at bay, requires a more or less fixed percentage of your innate immune activity.
If necessary, it can increase its activity so it can handle novel threats at the same time it’s doing everything else.
And you know when it’s doing that.
That’s when you feel like crap.
So what happens if you experience a radical increase in the need for a heightened innate immune response that exceeds its capacity?
One thing that happens is that its ability to successfully carry out its normal housekeeping that you never even notice is eroded.
When this happens, things slip by, whether neoplasms or certain viruses (or bacteria) the activity of which it’s been suppressing.
That is why immune-compromised people have increased rates of certain types of diseases and cancers rarely seen in younger people.
The way HIV does that is by infecting CD4 cells. The fewer CD4 cells you have the more likely it is that things will get out of control.
So the immune systems are always suppressing something. And when the immune system activity is suppressed then it can’t as easily suppress everything it needs to.
That can happen for one of two reasons:
1. By reducing the total number of immune resources or
2. By increasing the number of things it has to deal with.
Attacking the CD4 cell population reduces the total amount of resources and is an example of 1.
An example of 2 would be someone shooting you up with a load of virus. Oh, yeah, and infecting healthy cells in multiple organ systems simultaneously throughout your body with viral genes. Both of those will cause the innate immune system to have to respond.
And the more time and effort it’s spending on that, the less time and energy it has to devote to its every day stuff.
And, so, things formerly kept under control get out of control.
But that’s not because what’s causing the innate immune system to squander its resources is making something that’s bad to become inherently worse.
It’s because the innate immune system doesn’t have enough stuff to go around and things slip by. What kind of things? The things that were going on all the time but were being held in check.
So if you have a police force of 100 that can handle stuff and you reduce it to 10, then things will slip by.
Sort of like what the defund the police movement is aiming for.
And if you have a police force of 100, but your increase what it has to deal with tenfold, then you will also have things slipping by.
Sort of like what the open border and sanctuary cities movement was aiming for.
And guess what happens when both happen at the same time.
HIV reduces the CD4 police force.
The viral mRNA products, by producing large quantities of viral protein, increases what the same size police force has to deal with, and things will still slip by.
And the truly sick thing is that all of that was known decades ago and yet they did it anyway.
What will be done? I want to see those responsible indicted and prosecuted. Pfizer murdered my sweet husband and these criminals need to pay. I’m waiting and watching. I’m tired of just talk. 👁️👁️
I want the doctors and hos[ptals held accountable too, along with the Pols who sent elderly into covid riddled Nursing Homes.
I totally agree. I’m waiting!
I'm tired if waiting. Getting FURIOUS in the process, just like you...
Exactly. I live without my sweet husband that Pfizer murdered without recourse. I inform everyone in my life to never listen again and to take spike protein detox if they got jabbed. Some listen, most don’t cause they are not suffering, yet.
People are like cult members. They know something bad is happening, but they don't know who is causing it, and they don't know what to do. Time will open their eyes, and unfortunately, I know after FIVE YEARS of trying to warn people and losing nearly ALL my friends, people have to be DE-PROGRAMMED, like cult members, because they are victims of terrorism without knowing who is doing the terror.
Exactly. Herded sheep with Covid brain.
Welcome to my world! Five years now, and other issues before that! It's time to put the Tyranny back in the sewer where it belongs before it rips our planet apart. I've been hoping people would start "catching on," and-- they ARE. It's GOOD!
There is no such thing as a "covid-riddled" anything. There is no evidence of any virus, EVER. There is only people telling us there are viruses. What is far more likely is that your loved ones and friends have been harmed and killed by the "cure"-- the vaccine. It is shown, first by a Spanish laboratory called "La Quinta Columna," that at least some of those vials of "vaccine" were loaded with hard-core toxins, like mercury, lots of aluminum, graphene oxide... and more. ALL injections are now shown to be the wrong thing to do, and ALL vaccines contain toxins! Just leave it and go to a Naturopath! The symptoms of most illnesses are Nature's way of DETOXING the stuff causing the troubles. We're only now beginning to see the amazingly beautiful system our bodies have been endowed with, BY OUR CREATOR. xo
The SV40 virus can be the culprit if people have gene mutations and took the Pfizer or Moderna jabs. Kevin McKernan a gene expert in Canada talks about it being a death sentence. You can watch his videos about it. The PLANDEMIC OF FEAR INDUCED MANDATED POISON JABS. 💉💉💉💉💉
Well, I can’t make anyone believe or disbelieve anything, but I am completely convinced that viruses do not exist. Period. As for jabs, I wouldn’t touch one with a barge pole. If the Nasties make it to mandating death jabs, you can bet that will be the time of insurrection, if it hasn’t started already.
I think I may have answered this already, but it’s here in my “feed” again… ;)
I won’t get any jabs either.
This is why I like you. ha
There are no VIRUSES. It started out as a mistake, and became a VAST money-maker with the vaccines, so it hasn’t quite gone away… Don’t worry, NO virus has EVER been isolated!
I never feared anything covid. All one big scam. It still surprises me how much it affected so many with fear. They don’t get what was done to them. More will get sick, more will pass.
They won’t get sick from a VIRUS. But they will most likely get sick from 5G, and fluoride, and aluminum, and glyphosate… watch this:
https://youtu.be/4ml2S1mimPM
I want Heads in Baskets. Where are the WANTED posters with BOUNTIES and D.O.A. option???
Yes John, where are they? These criminals so far have been free to deceive and murder innocent people thru mandated poison shots. I’m infuriated.
Got it. I am seriously PISSED OFF. Practicing my AIM.
Try not to let it take over your brain... We are going to need level-headed, CALM responses to this in order to bring this down... They've been planning this for DECADES, and they are PREPARED, and we are not.
It’s not but it makes me sad for my husband. He was a great guy. I’m strong and dedicated. 👍
WE SHALL PREVAIL. They cannot win, because we MUST.
https://markgresham.substack.com/p/reimagining-hell
I'm so sorry about your husband. xo xo
Thank you! 😢
Hugs are coming to you, m'dear.
😊it’s been hard. When someone comes to your door and shoots to kill, you can indict and prosecute. But when Pfizer and all cohorts murdered my sweet husband, I just can’t get a grip on it. The responsible parties lists are enormous. I see nothing happening that would show me anyone cares. Hopefully RFK Jr. cares. As time goes on more victims will be evident, maybe then when it’s their loved one, caring will begin. Thanks for your notes.
And I suggest you think of things this say: Anybody who is in power politically is likely part of the Nastiness, or they’re unwitting dupes. This is much much bigger than a fake virus.
Oh yeah, much bigger.
Anytime. There are many things these days we can’t get a grip on… Don’t feel ALONE! Here if you ever want a chat. xo
😌
Only took them over 4 years.
Had to get everyone injected first so they would have cancer.
,… and they are still on the market 🤬
!!???!!!??!!???!!
Why? The data is overwhelming
Precisely.
Not everyone believes the truth.
People KNOW something is going on, but not everyone is trusting THE RIGHT PEOPLE.
Indeed! Still jabbing poor folks with this DOOM.
And the PCR is NOT A TEST, it doesn't diagnose anything, and even our own folks who are the Resistance use this phrase, "PCR Test," which enrages me because it is used to LIE to people so they keep getting the JAB!!!!! Makes me so furious.
At what point will the dam burst and we get the unvarnished truth along with Justice?
It seems, unless we MAKE it happen, it's not going to happen...
It WILL happen. The wave is building, and I think it'll be relatively soon... THIS YEAR, at the latest. That's my guess.
Met with with a friend for golf and she told me that 3 of her friends just died of heart attacks & strokes. All in their 70s.
I also know of people in their 40s with cancer.
One single person listened to me and didn’t get the shot—my husband. He’s thanked me many times since for my stubbornness.
Smart people.
THIS IS GENOCIDE. We all would do well to get this clear!
There were no MISTAKES. There is no OOPS. THIS IS GENOCIDE. Me, you can trust.
This should clear things up a bit... It's about an hour long. VERY GOOD VID.
https://youtu.be/4ml2S1mimPM
So much for "How Bad Is My Batch" reports...
Why are Gates and Fauchi and their cohorts not in jail? The evidence is overwhelming of their crimes against humanity. The pardons,the fool Obiden auto signed, aren’t worth the paper they are written on. Why are these murderers still free to continue their obsession to kill us all off ??? Why are the poison jabs still on the market ??? Where has all the sanity gone? I was one of the lucky ones who didn’t take the bait but I have many friends who did get the jab. Their illnesses run the gamut from senility, disabilities to blood cancers. When is this madness going to stop and those responsible held accountable for their diabolical actions?
I wish I could answer your questions, but I can’t.
Because so far, those who could do what's right ARE IN ON THE THING. I'm telling y'all, this has been planned for DECADES. They will sacrifice those who are shown to be evil, when they need to. Because the people behind all this Don't Mind Killing.
Why does the Dear Leader always seem to get a pass?
https://gregreese.substack.com/p/ai-grid-and-mrna-shots-announced
https://unlimitedhangout.com/2025/03/investigative-series/the-dark-maga-gov-corp-technate-part-1/
https://unlimitedhangout.com/2025/03/investigative-reports/the-dark-maga-gov-corp-technate-part-2/
ALL the Five Eyes Govt's and many of Europe's leadership ARE IN ON THIS.
It's SO much bigger than "covid." It's a globalist coup and a global genocide. Yes, it sounds insane... IT IS INSANE. But there it is. I've been onto this for FIVE YEARS. Slowly, I've learned SO MUCH and none of it, well, hardly any of it, is GOOD. It does turn out, tho, that our bodies are a miraculous gift from our Creator, and getting a "vaccine" is never, ever, a good thing.
Problem is no truth in mRNA or DNA found in vials. Graphene Oxide is found in the vials. Micro Raman technology finds no organic material. We present here our research on the presence of graphene in covid vaccines. We have carried out a random screening of graphene-like nanoparticles visible at the optical microscopy in seven random samples of vials from four different trademarks, coupling images with their spectral signatures of RAMAN vibration. By this technique, called micro-RAMAN, we have been able to determine the presence of graphene in some of these samples, after screening more than 110 objects selected for their graphene-like appearance under optical microscopy. Out of them, a group of 28 objects have been selected, due to the compatibility of both images and spectra with the presence of graphene derivatives, based on the correspondence of these signals with those obtained from standards and scientific literature. The identification of graphene oxide structures can be regarded as conclusive in 8 of them, due to the high spectral correlation with the standard. In the remaining 20 objects, images coupled with Raman signals show a very high level of compatibility with undetermined graphene structures, however different than the standard used here. This research remains open and is made available to scientific community for discussion. We make a call for independent researchers, with no conflict of interest or coaction from any institution to make wider counter-analysis of these products to achieve a more detailed knowledge of the composition and potential health risk of these experimental drugs, reminding that graphene materials have a potential toxicity on human beings and its presence has not been declared in any emergency use authorization. We leave a link to download this report at the end of this video. https://www.researchgate.net/publication/355979001_DETECTION_OF_GRAPHENE_IN_COVID19_VACCINES
Not Surprised
And, there's this from yesterday's "Lioness of Judah" substack........
That's pretty harsh, pegging them as GMO's, but it brings a vital question to play.
The numbers reflecting a systemic "failure to reproduce" in vaxxed people is becoming alarmingly clear. Simply, not only this generation, but future gen's were also plagued. The miscarriages, stillborns, loss of menstrual cycles, etc. all point to significant reproduction issues.
Will purebloods become the breeding stock? Would you want your pureblood son or daughter to risk your future grandchildren with a vaxxed partner?
Onward, Christian soldiers!
What the fuck are "purebloods"? Are you living in Harry Potter world? lol
And yeah, Christians, and EVERYONE ELSE that is a Human Being... getcha head on straight, my friend, this is not the time to be hating on your fellow Humans. We are an ENDANGERED SPECIES right now. ALL people who believe in LOVE are worthy.
BREAKING: Dr. Peter Kotlár Drops Bombshell Investigation Into DNA Contamination: The Vaccinated Are Now Officially GMO!
"I’m not afraid to say officially— a genetically modified organism. "
LIONESS OF JUDAH MINISTRY
MAR 14
Does this help mr. herder?
Onward, Christian soldiers!
Well, you’re telling me something. Are you going to show me the PROOF of what you’re telling me? You may be right, but there are discussions about DNA, too. We’ve been told SO many lies, I don’t just accept something like that anymore, and besides, I’ve heard this already and I don’t trust it. :)
And I’m not a “mr.” either. But I sound like one, people tell me. Woof!
Hello, Ms. Herder (if this is incorrect, sorry, I only have two choices...)
I share your bewilderment, and the constant nagging desire to question and challenge everything, particularly authority. We don't trust anybody to tell us the complete truth anymore.
The intention of my post was more to post thought-provoking questions that will have to be acknowledged at some time, not to stir up hate and discontent.
My oldest grandson is posing situations right now that could have him enlisting in the Air Force after H/S graduation and marriage to a vaxxed young woman. I don't know the lucky lady, but I would bet she's a truly wonderful person with high morals. I hope you can see where this circumstance evolved into the post yesterday, and the true intentions.
These are difficult times, and this would be a very difficult topic in any environment. We were never equipped with tools to combat a treasonous gubmint, except the small arms of war. This is uncharted territory.
Onward, Christian soldiers!
Knowledge, Gbill7, Abigail, Mark Freeman, thanks for the restacks.
The news is not news, but that the FDA is saying that sure is.
It’s very disheartening to see things like this on other pages written with what seems either an almost a flagrant disregard for the immunological basis of what’s going on or a conscious attempt at sensationalism.
And given the actual primary mechanism of action common to ALL the viral mRNA products that I have described in detail for years, such sensationalism is only gilding the lily.
How do I know what exactly what the primary mechanism of action is?
Because I have used it more times than I can count since the late 1990s in my doctoral research in molecular neurobiology and then in my post-doctoral fellowship on a cardiology training grant in a neurobio/pharm/phys lab.
And it’s THIS stuff that has to be understood to be able to sort through all the weird stories that have flooded the internet since late 2020.
The real mystery, yet to be fully explained, was why both principal groups of critics of those products were as mum about it as the companies producing the products were.
There were two groups of critics, 1. The sensationalist “snake venom, 5G self-assembling nanobots, aborted fetuses, HIV, etc,” and 2. The more mainstream science-appearing guys appearing in groups to talk to Ron Johnson on Capitol Hill.
The first I believe were probably funded by the viral mRNA companies themselves to make all critics of the products look like completely hysterical morons.
The second is much more problematic for two reasons:
1. They talked about everything BUT the primary mechanism of action common to all those products, and
2. Any of them that had any real research experience in molecular biology knew exactly what it was before any of those companies announced in the latter part of 2020 that they would be using “viral mRNA.”
Here is what someone like Robt Malone would have known: in molecular biology the four most stupendous discoveries/innovations and upon which virtually all research in molecular biology depends, were (not in any particular order):
1. PCR,
2. Simple, quick, easy to use, and reliable Sanger DNA sequencing,
3. Restriction enzymes, and
4. Cell transfection reagents or techniques.
How so?
Part 1 of several.
Part 2 of several
When I wanted to figure out what was going on in cell-cell adhesion due to the developmentally-driven expression of a certain class of neural cell adhesion molecules responsible for neural pathfinding, neuron bundling, and nerve insertion into the target tissue, I needed a way to examine the roles carried out by the different domains of the cell adhesion molecule: the extracellular domain that bound in a homophilic and irreversible fashion to other such molecules on other cells, the transmembrane domain that kept in place, and the cytoplasmic domain that, eventually, would bind to cytoskeletal proteins and result in signal transduction, driving the developmental process. Some of the questions were:
1. What are the minimum conditions for cell-cell adhesion?
2. What are the minimum conditions for the recruitment of cytoskeletal proteins to the cytoplasmic domain of this class of cell adhesion molecule,
3. What is the order in which these events take place, especially the events downstream of cell-cell adhesion that recruit first one cytoskeletal protein to the cytoplasmic domain and then, following that, other cytoskeletal proteins to bind to them in order to activate gene expression in those cells in a developmentally favored way?
To do that, I would need:
A. to be able to identify the parts of the gene responsible for the different domains in the protein. It was PCR and DNA sequencing that made this possible.
B. to be able to chop those different domains apart at will. It was restriction enzymes that cut apart DNA at specific locations that made this possible.
C. to be able to assemble the DNA for the cytoplasmic/transmembrane domains with the DNA for the green fluorescent protein so I can track in real time where those extra cellular domains are in the membrane. It was PCR and sequencing that enabled me to see if I had successfully gotten the different fragments ligated in the proper order and correct orientation.
D. to be able to assemble the DNA of an extracellular domain with no binding activity from some other protein with the cytoplasmic domain of the cell adhesion molecule so I could selectively control, by the use of primary antibodies specific to that extracellular domain and secondary antibodies that bind to the primary, the aggregation of the cytoplasmic domains of the cell adhesion molecules in the absence of the cell adhesion molecule’s extra cellular domain. If this resulted in the selective binding of the cytoskeletal proteins, then it would mean that the cytoskeletal binding was controlled only by the propinquity of the cytoplasmic domains and that the role of the extracellular domain binding to others on another cell in contact served to concentrate them enough that the two binding domains on the cytoskeletal protein can bind to two different cytoplasmic domain of the cell adhesion molecule. It was PCR and sequencing that enabled me to see if I had successfully gotten the different fragments ligated in the proper order and correct orientation.
E. to be able to see any of that happening in living cells, I had to have a way of getting my gene constructs inside identical cells of a stable, well-characterized, immortal cell line. It was the use of either of two cell transfection reagents that enabled me to do that. One type was like that used by Pfizer. The other types were like those used by Moderna and Johnson&Johnson. I knew about but had no reason to use the adenovirus method used by AstraZeneca.
Everything I described above are just basic molecular biology techniques.
End part 2 of several
Part 3 of several
In the work I and hundreds of thousands of other molecular biologists did, we didn’t have to worry about the effects of innate or adaptive immune response for one simple reason: monocultures of immortal cells lines don’t HAVE innate or adaptive immune systems.
We also didn’t have to worry about those cell transfection reagents getting our gene constructs into any cell they bumped into. For us, it was the more, the merrier.
The viral mRNA companies did nothing but take decades-old reagents and techniques for dangerous off-label uses to introduce viral genes into healthy cells. And since those products carrying the viral genes would enter into any cells in any organs they bumped into, this meant those viral genes would be used in all those cells to produce in an uncontrolled manner many copies of a full length, physiologically-useless, but biologically-active viral protein.
And what would be the inevitable consequences of that?
Well, as Pfizer described it, “Our product only gives your body the information it needs to build immunity.”
But what they did NOT say was that the product-compromised cells, because of built-in internal sensors, would detect the simultaneous presence of viral mRNA and viral protein and then signal the innate immune system to launch innate immune inflammatory attacks to kill those cells.
Why does that happen?
Because the simultaneous detection of viral mRNA and viral protein is the minimum necessary condition to indicate viral infection that is in the replication phase. This is a disease process.
But the intensity of the innate immune system is a hierarchy of responses. The more signaling, the greater the response. The greater the number of organ systems involved, the greater the response.
Now, all that is happening before any member of the innate immune system comes into physical contact with a single viral protein. It’s happening before the adaptive immune system is ever involved.
Large enough innate immune inflammatory attacks just at that initial level can kill.
In an actual viral infection, that’s going on from the earliest time points, but it’s happening locally and a restricted manner.
And when a few viruses escape the innate immune inflammatory attacks, they can be physically detected by the innate immune system. And if you have an existing adaptive immune response to some of those proteins, they will start being tagged by antibodies and attacked by T cells. But still, it’s going on at the earliest timepoints and in restricted ways.
But with the viral mRNA products, everything starts out at a greatly elevated level of response. First with the innate immune inflammatory attacks on product-compromised cells in multiple organ systems.
Then there’s the appearance everywhere of the viral proteins.
Some may think, “Yeah, but they’re not viruses.”
That’s irrelevant because the innate and adaptive immune systems do not detect viruses or bacteria. They detect only viral and bacterial proteins (and some pathogen-specific glycosylation).
The adaptive immune system does NOT make specific antibodies and T cells against viruses or bacteria. It makes antibodies and T cells that are specific only for epitopes on individual viral and bacterial proteins.
And this is why injecting someone with a bunch of viral proteins, especially a broad variety of viral proteins, will create the same kind of adaptive immune response that exposure to an actual virus will--except without getting infected.
But in the case of the viral mRNA products, the big flood of viral proteins released following innate immune inflammatory attacks will be detected as viruses by the innate immune system as it comes into contact with them. And the greater the number of contacts, the greater the volume of those contacts, and the greater the number of organ systems involved, the greater the level of innate immune response--on TOP of that initial provocation at the cellular level.
And everything I described above in this part is just basic immunology. It’s something that many people employed by all those companies should have understood.
I understood it.
And even Robt Malone understood it. He said, “No one should be getting viral genes as a vaccine, especially not the way they’re doing it.”
But for years that very guarded and tepid response was the closest that anyone in that second group of critics came to describing the primary mechanism of action common to all those products.
And it was years until anyone was coming anywhere close to what I had been describing for years.
There is no satisfactory reason for that.
End part 3 of several
Part 4 of several
Now, based on all the above, one will have all he needs to understand that the viral mRNA products do not “cause” cancer.
And, in a related story, the viral mRNA does NOT “awaken” the “world’s deadliest virus.”
Here is what is actually going on.
In addition to an innate immune system, the human body, like all vertebrates also has an adaptive immune system.
The only time anyone really notices the innate immune system is either after getting a cut or scratch or scrape when you get a little inflammation around the wound or when you’re “coming down” with something.
In the latter case you are NOT feeling the effects of whatever you’re “coming down” with.
You are feeling the effects of your innate immune system gearing up to fight it.
Sniffles, coughing, sore throat, aches and pains, a fever, crankiness, ALL that is caused by your innate immune system.
You know how we know that?
You know the expression “snot-nosed kid”? You know why most kids, by the time they’re older children and teens, are no longer snot-nosed kids? It’s because through their repeated encounters with any of almost 200 common cold viruses, they have been gradually building up a general immunity against developing serious clinical cases.
They’re still getting infected. No one EVER stops getting infected. But the greater your repertoire of antibodies and T cells, the less work your innate immune system has to do to put it down.
And since many families of common cold viruses have varying numbers of viral proteins in common and since neither the innate nor adaptive immune systems recognizes viruses or bacteria, only viral or bacterial proteins, then each type of cold you get will boost your response to proteins your adaptive immune system already recognizes and your adaptive immune system will design new antibodies and T cells against the balance of proteins it’s encountering for the first time.
The more times you get infected, the greater your adaptive immune repertoire and the less work your innate immune system has to do. The less your innate immune system has to do, the less you notice it.
So when you don’t feel sick, it’s not that your innate immune system is not doing anything, it just doesn’t have to do as much.
But all the while, it’s constantly encountering and destroying stuff every day. There are certain viruses that keep replicating at a very low rate for a variety of reasons, but since their number is kept low by both the innate and adaptive immune system, you never notice it.
Why?
Because your adaptive immune system doesn’t get spun up enough for you to feel it.
So in the absence of some new virus, your innate and adaptive immune systems are maintaining a status quo whereby things are kept in check.
Doing that, whether it’s spotting and taking out neoplasms or foreign bacteria or viruses or holding stuff at bay, requires a more or less fixed percentage of your innate immune activity.
If necessary, it can increase its activity so it can handle novel threats at the same time it’s doing everything else.
And you know when it’s doing that.
That’s when you feel like crap.
So what happens if you experience a radical increase in the need for a heightened innate immune response that exceeds its capacity?
One thing that happens is that its ability to successfully carry out its normal housekeeping that you never even notice is eroded.
When this happens, things slip by, whether neoplasms or certain viruses (or bacteria) the activity of which it’s been suppressing.
That is why immune-compromised people have increased rates of certain types of diseases and cancers rarely seen in younger people.
The way HIV does that is by infecting CD4 cells. The fewer CD4 cells you have the more likely it is that things will get out of control.
So the immune systems are always suppressing something. And when the immune system activity is suppressed then it can’t as easily suppress everything it needs to.
That can happen for one of two reasons:
1. By reducing the total number of immune resources or
2. By increasing the number of things it has to deal with.
Attacking the CD4 cell population reduces the total amount of resources and is an example of 1.
An example of 2 would be someone shooting you up with a load of virus. Oh, yeah, and infecting healthy cells in multiple organ systems simultaneously throughout your body with viral genes. Both of those will cause the innate immune system to have to respond.
And the more time and effort it’s spending on that, the less time and energy it has to devote to its every day stuff.
And, so, things formerly kept under control get out of control.
But that’s not because what’s causing the innate immune system to squander its resources is making something that’s bad to become inherently worse.
It’s because the innate immune system doesn’t have enough stuff to go around and things slip by. What kind of things? The things that were going on all the time but were being held in check.
So if you have a police force of 100 that can handle stuff and you reduce it to 10, then things will slip by.
Sort of like what the defund the police movement is aiming for.
And if you have a police force of 100, but your increase what it has to deal with tenfold, then you will also have things slipping by.
Sort of like what the open border and sanctuary cities movement was aiming for.
And guess what happens when both happen at the same time.
HIV reduces the CD4 police force.
The viral mRNA products, by producing large quantities of viral protein, increases what the same size police force has to deal with, and things will still slip by.
And the truly sick thing is that all of that was known decades ago and yet they did it anyway.
Are you a Big Pharma investor?
Up yours you pig!
Vaccines might as well be called BIOWEAPONS, for all the good they do, for everyone but the Big Pharma investors.
You are a Big Pharma investor, folks, there you have it.
Not about vaccines, clearly not about vaccines.