Fauci’s diary does not prove Dr Shankara Chetty’s darkest interpretation. But it makes his early instinct—and the question he is now asking—much harder to dismiss.
Doctor, I have followed you for years and grreatly respect your rigor.
But before mid 2020 a Molecular Biologist colleague of mine ( ex-Genentech) told me he had “read to chinese spike protein sequence”, had seen the patented sequence, knew the patent holder and read the work that was patent basis and recognized the “invisible ligation” technique that had been used to insert it.
He said, “I had wanted to create this, I would have done it this way.”
Since that time I have confidently used the term “Malevolent Actors” to describe the drivers behind the COVID catastrophy. Dr. Chetty is correct.
The Gain of Function was needed to make something that was supposed to pandemic hard enough to go worldwide, yet soft enough to not kill everyone off the bat. The finer touches came with time.
They needed interferon suppression to create the asymptomatic spread.
They engineered Omicron to pull it out of the lower lung where it was killing, up to the upper airway for transmissiblity.
BTO and the Nanoparticle Revolution: ADEPT, P3, and the mRNA / LNP Blueprint
Before the creation of the Biological Technologies Office (BTO) in 2014, biological research was scattered across the Defense Sciences Office (DSO) and IPTO. Recognizing that biology was becoming an engineering discipline, DARPA created BTO to unify synthetic biology, novel therapeutics, and human performance.
The ADEPT Program and the Birth of Moderna’s Platform
In 2011, DARPA initiated the Autonomous Diagnostics to Enable Prevention and Therapeutics (ADEPT) program. The program was based on a radical hypothesis: instead of manufacturing complex proteins or weakened pathogens in industrial bioreactors over 12–18 months, the military could deliver genetic code directly into human cells, turning the human body into its own bioreactor to produce protective antibodies in days.
To make nucleic acid therapeutics (specifically synthetic messenger RNA) viable, two huge problems had to be solved:
RNA Instability: Raw mRNA breaks down almost instantly in the bloodstream.
Targeted In Vivo Delivery: Synthetic RNA must enter human cells without triggering immediate immune destruction before translation.
In October 2013, DARPA awarded a historic grant of up to $24.9 million under ADEPT to a young, pre-IPO startup named Moderna Therapeutics. At the time, mRNA therapeutics were widely viewed by mainstream academia and big pharma as too unstable and risky. DARPA’s funding was explicitly structured via Contracts Management to develop mRNA-encoded monoclonal antibodies against infectious diseases.
Key to this success was the development of Lipid Nanoparticles (LNPs)—microscopic spherical bubbles composed of ionizable lipids, cholesterol, and PEGylated lipids designed to encapsulate fragile mRNA constructs, navigate through the bloodstream, and fuse with cellular membranes.
The Pandemic Prevention Platform (P3) and Industrial Scale
Building on ADEPT, BTO launched the Pandemic Prevention Platform (P3) program in 2017. The objective was ambitious: deliver an FDA-approved or EUA-ready protective treatment within 60 days of identifying a novel threat.
Through P3, BTO funded a network of performers pushing nanoparticle engineering, gene encoding, and automated manufacturing:
Moderna: Advanced its automated mRNA sequencing and formulation pipeline.
AstraZeneca, Sanofi, and Merck: Integrated DARPA-funded platforms or engaged in licensing agreements to explore lipid-encapsulated nucleic acid delivery for broad viral targets.
Pfizer and BioNTech: While BioNTech was an independent European pioneer, BioNTech’s LNP formulations and mRNA delivery validation leveraged broader platform advancements spurred by DARPA’s early investments in the LNP supply chain and lipid chemistry validation.
When SARS-CoV-2 emerged in early 2020, Moderna used the exact automated mRNA design and LNP encapsulation infrastructure developed under DARPA’s ADEPT and P3 grants to generate sequence-ready vaccine candidates in days, moving to clinical trials in record time.
BLA, BLA, BLA, yes, all of it happened, so WHAT???
WHERE THE HELL you have that ONE AND ONLY, THE MOST CLASSIFIED WORD EVER SINCE covid PFizer/Mod-E-RNA injections: GENE THERAPIES, the word which could have RESCUED THE ENTIRE POPULATION OF THIS PLANET, if it was NOT FOR the DECEIVERS WHO CHANGED THE DEFINITION OF 'vaccines'?? IF ONLY PEOPLE KNEW EVERYONE WILL UNDERGO GENE THERAPY, GENE MODIFICATION TREATMENT WITH SYNTHETIC GENES, and that with NO RETURN, EVER, there wouldn't be a single covid shot applied!! That crime is committed by every single still working MD, and everyone else for that matter, who talks about 'vaccines' without telling the worst nightmare FACT behind the LIES.
The 'so what' part is that it explains everything neatly and simply without having to invent anything.
Our favourite Doctor MacMillan (and friends) has done a superb job of keeping the masses fueled with inspiration to keep pressing. This cannot be understated.
Pressing on GOF is crucial for all the same reasons it was "stopped" in the first place. This is bioweapons anti-proliferation. Virus engineering is mature. As aDoctor you cannot stop viruses. However we can stop vaccine approval and use.
The DARPA and BARDA programs set up the solutions for all the problems they have sitting in the database ready to print off.
They just used the plausibility of an escaped Novel Pathenogen to drive radical acceptance of Gene Therapies. I know, you get it.
Now they are just going to dump powdered LNPs on all the oceans to cure fin rot or something. They infected all the Deer with Covid, so maybe the meat is full of misfolded proteins.
Lots of room for globalist fears, but do not underestimate that DARPA is 100 years ahead of the WEF.
Methinks those percentages have now changed. Although I thought relying on vaccines (and particularly mRNA vaccines) to treat COVID was misguided, I believed "they" were trying to perform a public service that required mass-immunisation; something like what was used to remove polio and measles I thought. I now treat public health announcements with skepticism and avoid vaccines and medicines wherever possible.
“What was the Intention?” Depopulation! Get EVIL Bill Gates alongside Fauci for intense questioning. Anyone involved with Epstein (Bill Gates) cannot be trusted!!!
Dear Philip - I do not know Shankaras darkest interpretation - probably I missed it. But independently knowing a little bit of the entire industry, the TRILLIONS involved and more - TRILLIONS more to come . . . . creating cancer potential, then launching mRNAs against cancer - wow what a new infinite fountain of making money. Forget about human (rights). A human means nothing in the Pharma-Industry. People are used like we use cows and pigs to satisfy our hunger for meat. We breed them, we slaughter them. A human being on earth is nothing more than an animal in the end - or you want to have a different analogy? We are like the electrons which create electricity. We have to move from A to B - from birth place to the cemetery and on our way we move like electrons (we cost money, we consume, we earn & pay taxes, we must get sick so that we can pay for the medicines with which others make billions and even death or dying is a business . . . . . WOW - where did we end up between PhDs, MBAs, MDs - every year more academic education but mankind moves backwards, I feel. We have now enough evidence that this thing ws man-made, well-studied on most of its consequences (infertility, death risk, cancer risk . . . ) and to me it was clear - it was not a leak. It was distributed on purpose - because why was it made anyway - to keep it in the lab ?? Fauci invoking the 5th amendment is another prove that he was one of the really bad guys and key functions in this terrible crime against humanity - THE BIGGEST EVER ! I mean we can let it rest - because it happened (even though it was worse then HITLER & STALIN together !!) and we cannot change a thing. The only problem is - that if those key-drivers do not land in jail or even on an electric chair - this will go on and on and on. It grows like a cancer and a very aggressive one. The Ukraine war - even though it has nothing to do with Virae, Health, Medicine, Pharma - it is based on the same foundations as the pandemic. This war has killed already 2+ million men. Many of them died a terrible death on the battlefield - because they were not rescued. Or they were tortured to death from the AZOV battalion. Again we arrive at a scene where a human being is just "nothing". ZERO. We need to fight it because one day WE ARE THE VICTIMS of these same people who organize all of it with the force and power of SWARM-INTELLIGENCE !
I think the 'darkest interpretation' was "Gain of function and biologic research poses one of the greatest threats to humanity that’s ever been posed. It’s an extinctional type of development technology." Depopulation en masse, hence the reference to the Illuminati.
It is not frightenind to me to hear the content he is telling. It is just joy to listen to him because he is so clear minded.
Yes the agenda is about eugenics and depopulation.
There has been induced mass formation and also a lot of Gleichschaltung within the scientific community (and the whole western societies). The masterminds knew the plan and they forced it onto others. They knew what they were doing. Just let me give you one example. It is a citation from Dr. Sabine Stebel. When she did the scientific work to earn her Dr-title she wondered about the use of such stuff she was busy with, because any economic use of that was not in sight. Some twelve years later she realized what it had been about. She had done gain-of-function-research without knowing it. She claims being among the ten people in Germany with the best protein-engeniering skills. And now finally the citation I announced. It is about Professor Chichutek during the 'pandemic' president to the Paul-Ehrlich-Institut (PEI) the German institution to control vaccines. Dr. Stebel writes: "Chichutek had known about that stuff much earlier, the insights he published in his 2006 paper are showing this. He was a decade ahead to all of us."
Some of them knew very well what they were doing.
And to give you an answer to your question, why the push seems not to be going on. The goal aimed to with the 'vaccines' was not achieved - because we the people stopped them (Philantropaths) in doing so.
In 2020 their slogan was "you will own nothing and be happy" in 2023 their slogan was "rebuilding trust"
I hope Shankara understands why his "case has been pending for the past three and a half years".
The last thing his prosecutors can afford is to allow him to speak formally and publicly from the dock, so strong is his ability to perceive, analyse and articulate.
That's why they have resorted to the stain of a long-term legal persecution - a psychological stress with no end in sight.
Thankfully, it doesn't seem to be bothering him much!
Another clue is the way mRNA vaccines were promoted as being superior to adenovirus vector vaccines. The clinical trials advertised Moderna and Pfizer at 90% protection while J&J was advertised at 70%, but I have seen some studies showing they were all about 70% in the beginning. Then the side effects seemed to be advertised as a J&J problem even though I have seen studies showing they were all similar. So in the US it seemed that mRNA vaccines were the goal - not just vaccines. I think there was an urgent agenda to develop public trust in mRNA along with the infrastructure to rapidly deploy an mRNA vaccine in emergencies such as terrorist attacks and even biological warfare. There was probably also an agenda to gain worldwide leadership in a promising new mRNA industry for all sorts of medicines. The COVID emergency allowed them to move all that ahead many years faster by cutting corners and spending huge sums of money.
“In an elderly demographic, the baseline is already a rolling sea of noise,” Sarah interrupted, her expression calculated. “Older populations naturally present background rates of cardiovascular events, arrhythmias, and age-related cardiac decline. Any low-level inflammatory whisper or subtle cardiac blip gets instantly absorbed and lost in the sheer volume of pre-existing comorbidities.”
I am with Dr Chetty on this. This is a lab created virus.
Bill Gates is on record saying that he wants to cull 15% of the population to save the planet and that vaccines present the only way to do this without a backlash.
For Big Pharma it was about forcing the acceptance of the MRNA platform on the public ,whether they wanted it or not.
And now Big Pharma is bringing out MRNA versions of every vaccine.
So this is much bigger than COVID, every MRNA pseudo - vaccine forced upon the public will be as deadly as the COVID gene therapy injections. None of them will confer immunity.
But the profits for Big Pharma will be off the scale.
To write on these points without discussion of the endgame is to miss the elephant in the room, namily the pretext for injections. All of this upfront drama: the leaked china videos, the emergency approvals, thefear, the EUAs, false and faulty pcr tests, inaccurate patient death models provided pretext for deploying mRNA injections to make possible this trillion $ industry.
I wonder how many vaccinated in the womb will be able to reproduce and if they can, what DNA are the female eggs going to reproduce. They are still targeting pregnant women.
As always, your calm, analytical, and clear presentation of this enormous problem creates the level of understanding that enables the concerned public to have constructive discussions with others. Knowledge and curiosity are fearless and catching! Thank you!
Fauci didn’t do this for fame or money. He did it because he’s part of the predator class elite that concocted an mRNA vaccine that give specific instructions to the bodies cells to reproduce the exact same spike protein from the Wuhan lab.
We are in a perpetual state of spike production. We are spike production factories. Nobody knows how to turn it off. Don’t you think that’s a problem? 
Not jabbed. Question is even if 5day fasting doing and resetting completed what happens if reinfection occurs (if a person lives in highly jabbed country) and cycle of symptoms recur. Is this then a 5 day fast repeat.
Thanks for the wonderful info on fasting. 67+ old not jabbed.
The nice thing about planned fasting is that you can schedule it.
So you can do it every decade
every year
every month
I fasted for 10 days before and learned that 5 days was correct. I kept going with the fast because i could - but it was 2 years before my stomach digested properly again. I ate too much of myself, but passing on the info to others makes it worth gaining in the first place.
So really fasting shouldn't be seen as an intervention, so much as periodic preventative maintenance. Lots of cultures preserve the basic knowlege - some religions do it annually. No doubt there is a Californian that eats 3 days on and 3 days off lol. It depends of course on the person, and constituency.
The Sars-Cov2 VIRUS was equipped with 2 nasty proteases that go around the infected cell and start chopping up host proteins. They do not get a lot of attention - but they were nasty. My hypothesis is autoimmunity - not from what the virus made, but from what it destroyed - self.
Because the virus was engineered with the furin cleavage site, and gained entry with ACE2 - it was a bat poison that was given a backstage pass to every cell in the human body - when normally a bat virus would be locked out. If they didn't do the gain of function then Sars-Cov2 would have been less than a cold. But they did, and whatever cryptic layers they engineered into it will unfold in the host. But it is a damage that evenually get's stopped by the normal immune system. A flooded basement might be ruined, but it will be dry in beween floods. There can be damage - but it's not an ongoing damage in general. So a fast is likely to not do much unless you suspect your immune system picked up immunity to the foreign bug, AND yourself.
the case of vaccination is way worse - there are many more things wrong about the LNP transfection platforms. LNP damages, biodistribution from LNP size variation and vroman effect making spike where viruses never reach. for time way longer than a virus acts.
in the case of infection the virus makes more copies of itself - and then tries to make you sneeze - it needs all the arms and legs it made for itself in your cell when it's mother virus invaded and started using it for parts.
in the case of the vaccine, it was not a case of a virus making children with arms and legs and spike proteins as per the virus recipe. the LNP was just a work order to make thumbs. a trillion LNPs, with each mRNA fragment making 1000-5000 copies of thumbs (spike protein only - no other virus parts).
so the vaccine will fill you up wth 1000x too much antigen - enough to flash-bang the natural immune system to making the same knee jerk reaction for every future infection....
thumbs EVERYWHERE - in the brains, ovaries, adrenal glands..
so vaccination problems need the 'cleanup' more than infection.
infection is the single best vaccination and offers the most immunity - not just a wanted poster for Hitler showing only a short mustache
but people got covid 6 times so that tells you that vaccines are literally useless. Omicron IS the airborne vaccine - avoid it like you avoid vaccination. but of you catch Omicron again, your vaccine is up to date.
Doctor, I have followed you for years and grreatly respect your rigor.
But before mid 2020 a Molecular Biologist colleague of mine ( ex-Genentech) told me he had “read to chinese spike protein sequence”, had seen the patented sequence, knew the patent holder and read the work that was patent basis and recognized the “invisible ligation” technique that had been used to insert it.
He said, “I had wanted to create this, I would have done it this way.”
Since that time I have confidently used the term “Malevolent Actors” to describe the drivers behind the COVID catastrophy. Dr. Chetty is correct.
"If This Was Gain-of-Function, What Was the Intention?"
isn't it obvious, that the answer is: a UNIVERSAL gene therapy without consent, described widely and deceptively as 'GOF'...
The Gain of Function was needed to make something that was supposed to pandemic hard enough to go worldwide, yet soft enough to not kill everyone off the bat. The finer touches came with time.
They needed interferon suppression to create the asymptomatic spread.
They engineered Omicron to pull it out of the lower lung where it was killing, up to the upper airway for transmissiblity.
BTO and the Nanoparticle Revolution: ADEPT, P3, and the mRNA / LNP Blueprint
Before the creation of the Biological Technologies Office (BTO) in 2014, biological research was scattered across the Defense Sciences Office (DSO) and IPTO. Recognizing that biology was becoming an engineering discipline, DARPA created BTO to unify synthetic biology, novel therapeutics, and human performance.
[ DARPA ADEPT Program (2011) ]
│
┌───────────────────────┴───────────────────────┐
▼ ▼
[ Moderna Seed Funding (2013) ] [ LNP & Carrier Tech ]
(Up to $25M OTA Grant) (In Vivo Delivery Systems)
│ │
└───────────────────────┬───────────────────────┘
▼
[ DARPA P3 Program (2017) ]
(60-Day Pathogen-to-Protection)
│
▼
[ COVID-19 Commercialisation (2020) ]
(Moderna, Pfizer/BioNTech, Sanofi, Merck)
The ADEPT Program and the Birth of Moderna’s Platform
In 2011, DARPA initiated the Autonomous Diagnostics to Enable Prevention and Therapeutics (ADEPT) program. The program was based on a radical hypothesis: instead of manufacturing complex proteins or weakened pathogens in industrial bioreactors over 12–18 months, the military could deliver genetic code directly into human cells, turning the human body into its own bioreactor to produce protective antibodies in days.
To make nucleic acid therapeutics (specifically synthetic messenger RNA) viable, two huge problems had to be solved:
RNA Instability: Raw mRNA breaks down almost instantly in the bloodstream.
Targeted In Vivo Delivery: Synthetic RNA must enter human cells without triggering immediate immune destruction before translation.
In October 2013, DARPA awarded a historic grant of up to $24.9 million under ADEPT to a young, pre-IPO startup named Moderna Therapeutics. At the time, mRNA therapeutics were widely viewed by mainstream academia and big pharma as too unstable and risky. DARPA’s funding was explicitly structured via Contracts Management to develop mRNA-encoded monoclonal antibodies against infectious diseases.
Key to this success was the development of Lipid Nanoparticles (LNPs)—microscopic spherical bubbles composed of ionizable lipids, cholesterol, and PEGylated lipids designed to encapsulate fragile mRNA constructs, navigate through the bloodstream, and fuse with cellular membranes.
The Pandemic Prevention Platform (P3) and Industrial Scale
Building on ADEPT, BTO launched the Pandemic Prevention Platform (P3) program in 2017. The objective was ambitious: deliver an FDA-approved or EUA-ready protective treatment within 60 days of identifying a novel threat.
Through P3, BTO funded a network of performers pushing nanoparticle engineering, gene encoding, and automated manufacturing:
Moderna: Advanced its automated mRNA sequencing and formulation pipeline.
AstraZeneca, Sanofi, and Merck: Integrated DARPA-funded platforms or engaged in licensing agreements to explore lipid-encapsulated nucleic acid delivery for broad viral targets.
Pfizer and BioNTech: While BioNTech was an independent European pioneer, BioNTech’s LNP formulations and mRNA delivery validation leveraged broader platform advancements spurred by DARPA’s early investments in the LNP supply chain and lipid chemistry validation.
When SARS-CoV-2 emerged in early 2020, Moderna used the exact automated mRNA design and LNP encapsulation infrastructure developed under DARPA’s ADEPT and P3 grants to generate sequence-ready vaccine candidates in days, moving to clinical trials in record time.
badprotein.substack.com/p/parsimony
badprotein.substack.com/p/infinite-improbability
BLA, BLA, BLA, yes, all of it happened, so WHAT???
WHERE THE HELL you have that ONE AND ONLY, THE MOST CLASSIFIED WORD EVER SINCE covid PFizer/Mod-E-RNA injections: GENE THERAPIES, the word which could have RESCUED THE ENTIRE POPULATION OF THIS PLANET, if it was NOT FOR the DECEIVERS WHO CHANGED THE DEFINITION OF 'vaccines'?? IF ONLY PEOPLE KNEW EVERYONE WILL UNDERGO GENE THERAPY, GENE MODIFICATION TREATMENT WITH SYNTHETIC GENES, and that with NO RETURN, EVER, there wouldn't be a single covid shot applied!! That crime is committed by every single still working MD, and everyone else for that matter, who talks about 'vaccines' without telling the worst nightmare FACT behind the LIES.
The 'so what' part is that it explains everything neatly and simply without having to invent anything.
Our favourite Doctor MacMillan (and friends) has done a superb job of keeping the masses fueled with inspiration to keep pressing. This cannot be understated.
Pressing on GOF is crucial for all the same reasons it was "stopped" in the first place. This is bioweapons anti-proliferation. Virus engineering is mature. As aDoctor you cannot stop viruses. However we can stop vaccine approval and use.
The DARPA and BARDA programs set up the solutions for all the problems they have sitting in the database ready to print off.
Nanoparticle Transfection Platforms delivering Prodrugs
- are not the same as --
Gain of Function Virus Engineering
They just used the plausibility of an escaped Novel Pathenogen to drive radical acceptance of Gene Therapies. I know, you get it.
Now they are just going to dump powdered LNPs on all the oceans to cure fin rot or something. They infected all the Deer with Covid, so maybe the meat is full of misfolded proteins.
Lots of room for globalist fears, but do not underestimate that DARPA is 100 years ahead of the WEF.
We got the data. The experiment ran.
80% will do anything they are told.
20% think for themselves.
Doesn't matter whether they are doctors or not.
Methinks those percentages have now changed. Although I thought relying on vaccines (and particularly mRNA vaccines) to treat COVID was misguided, I believed "they" were trying to perform a public service that required mass-immunisation; something like what was used to remove polio and measles I thought. I now treat public health announcements with skepticism and avoid vaccines and medicines wherever possible.
"The truth is that most people lack the intellectual ability and courage to resist a popular movement, however pernicious and ill-considered."
Ludwig von Mises (1947). "Planned Chaos," pg. 81, Ludwig von Mises Institute
…and ..
“What was the Intention?” Depopulation! Get EVIL Bill Gates alongside Fauci for intense questioning. Anyone involved with Epstein (Bill Gates) cannot be trusted!!!
Dear Philip - I do not know Shankaras darkest interpretation - probably I missed it. But independently knowing a little bit of the entire industry, the TRILLIONS involved and more - TRILLIONS more to come . . . . creating cancer potential, then launching mRNAs against cancer - wow what a new infinite fountain of making money. Forget about human (rights). A human means nothing in the Pharma-Industry. People are used like we use cows and pigs to satisfy our hunger for meat. We breed them, we slaughter them. A human being on earth is nothing more than an animal in the end - or you want to have a different analogy? We are like the electrons which create electricity. We have to move from A to B - from birth place to the cemetery and on our way we move like electrons (we cost money, we consume, we earn & pay taxes, we must get sick so that we can pay for the medicines with which others make billions and even death or dying is a business . . . . . WOW - where did we end up between PhDs, MBAs, MDs - every year more academic education but mankind moves backwards, I feel. We have now enough evidence that this thing ws man-made, well-studied on most of its consequences (infertility, death risk, cancer risk . . . ) and to me it was clear - it was not a leak. It was distributed on purpose - because why was it made anyway - to keep it in the lab ?? Fauci invoking the 5th amendment is another prove that he was one of the really bad guys and key functions in this terrible crime against humanity - THE BIGGEST EVER ! I mean we can let it rest - because it happened (even though it was worse then HITLER & STALIN together !!) and we cannot change a thing. The only problem is - that if those key-drivers do not land in jail or even on an electric chair - this will go on and on and on. It grows like a cancer and a very aggressive one. The Ukraine war - even though it has nothing to do with Virae, Health, Medicine, Pharma - it is based on the same foundations as the pandemic. This war has killed already 2+ million men. Many of them died a terrible death on the battlefield - because they were not rescued. Or they were tortured to death from the AZOV battalion. Again we arrive at a scene where a human being is just "nothing". ZERO. We need to fight it because one day WE ARE THE VICTIMS of these same people who organize all of it with the force and power of SWARM-INTELLIGENCE !
I think the 'darkest interpretation' was "Gain of function and biologic research poses one of the greatest threats to humanity that’s ever been posed. It’s an extinctional type of development technology." Depopulation en masse, hence the reference to the Illuminati.
Thank you for this brilliant analytic talk.
Dr. Chetty is completly right.
It is not frightenind to me to hear the content he is telling. It is just joy to listen to him because he is so clear minded.
Yes the agenda is about eugenics and depopulation.
There has been induced mass formation and also a lot of Gleichschaltung within the scientific community (and the whole western societies). The masterminds knew the plan and they forced it onto others. They knew what they were doing. Just let me give you one example. It is a citation from Dr. Sabine Stebel. When she did the scientific work to earn her Dr-title she wondered about the use of such stuff she was busy with, because any economic use of that was not in sight. Some twelve years later she realized what it had been about. She had done gain-of-function-research without knowing it. She claims being among the ten people in Germany with the best protein-engeniering skills. And now finally the citation I announced. It is about Professor Chichutek during the 'pandemic' president to the Paul-Ehrlich-Institut (PEI) the German institution to control vaccines. Dr. Stebel writes: "Chichutek had known about that stuff much earlier, the insights he published in his 2006 paper are showing this. He was a decade ahead to all of us."
Some of them knew very well what they were doing.
And to give you an answer to your question, why the push seems not to be going on. The goal aimed to with the 'vaccines' was not achieved - because we the people stopped them (Philantropaths) in doing so.
In 2020 their slogan was "you will own nothing and be happy" in 2023 their slogan was "rebuilding trust"
We stopped them but the fight is not yet won.
The over-use of the phrase "Build Back Better" all around the world is further evidence of a coordinated agenda.
Dr Chetty's success in treating the victims was an obstacle to any depopulation program, hence his continued punishment by legal persecution.
I hope Shankara understands why his "case has been pending for the past three and a half years".
The last thing his prosecutors can afford is to allow him to speak formally and publicly from the dock, so strong is his ability to perceive, analyse and articulate.
That's why they have resorted to the stain of a long-term legal persecution - a psychological stress with no end in sight.
Thankfully, it doesn't seem to be bothering him much!
Intentions … the Light of ‘Do or Die’, Happy or Sad, Slave or Free
I somehow feel 'Get off scot-free' should be blended into this drink.
That's an intention right?
Another clue is the way mRNA vaccines were promoted as being superior to adenovirus vector vaccines. The clinical trials advertised Moderna and Pfizer at 90% protection while J&J was advertised at 70%, but I have seen some studies showing they were all about 70% in the beginning. Then the side effects seemed to be advertised as a J&J problem even though I have seen studies showing they were all similar. So in the US it seemed that mRNA vaccines were the goal - not just vaccines. I think there was an urgent agenda to develop public trust in mRNA along with the infrastructure to rapidly deploy an mRNA vaccine in emergencies such as terrorist attacks and even biological warfare. There was probably also an agenda to gain worldwide leadership in a promising new mRNA industry for all sorts of medicines. The COVID emergency allowed them to move all that ahead many years faster by cutting corners and spending huge sums of money.
Hi Bob,
They wanted it for the army, but the manufacturers wanted it for everyone.
The conspiracy is not a theory, and the theory is not a conspiracy.
The programs were called ADEPT and P3.
DARPA hires scientists for 5 years. Thats the deal.
Look at the Offices.
Look at the Support Offices.
These people design weapons, seed companies to make them, and even take care of all that pesky regulatory capture that is needed.
Office of the Secretary of Defense
[ Under Secretary of Defense for Research & Engineering ]
(USD(R&E) / DoD Chief Technology Officer)
│
▼
Defense Advanced Research Projects Agency
[ DARPA Director ]
│
┌───────────────┴───────────────┐
▼ ▼
[ 6 Technical Offices ]
- BTO (Biology)
- DSO (Defense Sciences)
- IPTO (Info Processing)
- MXO (Multi X / Microsystems)
- STO (Strategic Tech)
- TTO (Tactical Tech)
[ Support Offices ]
- Legal Counsel
- Contracts Management
- Legislative Affairs
- Commercial Strategy
https://badprotein.substack.com/p/mission-accomplished
https://badprotein.substack.com/p/darpasoft
Thanks, that is interesting detail.
I Plead the Fifth - of August
“In an elderly demographic, the baseline is already a rolling sea of noise,” Sarah interrupted, her expression calculated. “Older populations naturally present background rates of cardiovascular events, arrhythmias, and age-related cardiac decline. Any low-level inflammatory whisper or subtle cardiac blip gets instantly absorbed and lost in the sheer volume of pre-existing comorbidities.”
https://badprotein.substack.com/p/i-plead-the-fifth-of-august
I am with Dr Chetty on this. This is a lab created virus.
Bill Gates is on record saying that he wants to cull 15% of the population to save the planet and that vaccines present the only way to do this without a backlash.
For Big Pharma it was about forcing the acceptance of the MRNA platform on the public ,whether they wanted it or not.
And now Big Pharma is bringing out MRNA versions of every vaccine.
So this is much bigger than COVID, every MRNA pseudo - vaccine forced upon the public will be as deadly as the COVID gene therapy injections. None of them will confer immunity.
But the profits for Big Pharma will be off the scale.
...and depopulation will also continue. Georgia Guidestones: Population to be kept at under 500,000,000.
To write on these points without discussion of the endgame is to miss the elephant in the room, namily the pretext for injections. All of this upfront drama: the leaked china videos, the emergency approvals, thefear, the EUAs, false and faulty pcr tests, inaccurate patient death models provided pretext for deploying mRNA injections to make possible this trillion $ industry.
I wonder how many vaccinated in the womb will be able to reproduce and if they can, what DNA are the female eggs going to reproduce. They are still targeting pregnant women.
As always, your calm, analytical, and clear presentation of this enormous problem creates the level of understanding that enables the concerned public to have constructive discussions with others. Knowledge and curiosity are fearless and catching! Thank you!
https://sashalatypova.substack.com/p/the-covid-dossier-updated-a-record?utm_source=substack&utm_medium=email
https://oversight.house.gov/wp-content/uploads/2024/12/12.04.2024-SSCP-FINAL-REPORT.pdf
Fauci didn’t do this for fame or money. He did it because he’s part of the predator class elite that concocted an mRNA vaccine that give specific instructions to the bodies cells to reproduce the exact same spike protein from the Wuhan lab.
We are in a perpetual state of spike production. We are spike production factories. Nobody knows how to turn it off. Don’t you think that’s a problem? 
They killed us.
Nobody is coming to save us.
#WalkingScienceExperiment
 READ THIS💥 💥
👉 https://oversight.house.gov/wp-content/uploads/2024/12/12.04.2024-SSCP-FINAL-REPORT.pdf
HERE ARE SOME ASTOUNDING FACTS located around pages 300+
V. Vaccine Mandates Were Not Supported by Science and Caused More Harm than Good
..........................................................................................................................................page 336
A. COVID-19 Vaccine Mandates Caused Massive Collateral Damage and Were Very
Likely Counterproductive ..........................................................................................page 340
B. COVID-19 Vaccine Mandates Were Not Supported by Science ...............................346
C. COVID-19 Vaccine Mandates Hampered U.S. Military Readiness ..........................347
VI. The COVID-19 Vaccine, While Largely Safe and Effective, Had Adverse Events That
Must be Thoroughly Investigated ....................................................................................349
A. The Vaccine Adverse Event Reporting System is Insufficient and Not Transparent .......
....................................................................................................................................349
B. Existing Vaccine Safety Systems May Be Missing Important Safety Signals,
Especially Related to Neurological Conditions .........................................................353
C. The U.S. Centers for Disease Control and Prevention Created a new Surveillance
System Specifically for COVID-19 Vaccines but Has Not Been Fully Transparent in
Sharing the Data Collected in it .................................................................................355
VII. The U.S. Government’s Insufficient Systems for Compensating COVID-19 Vaccine
Injuries .............................................................................................................................357
A. The U.S. Government Is Failing to Efficiently, Fairly, and Transparently Adjudicate
Claims for COVID-19 Vaccine Injuries .....................................................................359
B. The Countermeasure Injury Compensation Program Failed to Handle a Mass-
Vaccination Program ..................................................................................................361
C. A Robust and Transparent Vaccine Injury Compensation Program Is Necessary for
Promoting Trust in Vaccines ......................................................................................363
D. Debating or Discussing Vaccine Injury Compensation is Not “Anti-Vax,” and
Implications Otherwise Are Counterproductive to Protecting Public Health ............364
VIII. The Erosion of the Doctor-Patient Relationship During the COVID-19 Pandemic ........366
A. Pandemic-Era Policy Often Disregarded or Outright Violated the Sanctity of the
Doctor-Patient Relationship .......................................................................................367
B. The Use of Off-Label Prescriptions Was Unjustly Demonized and Further Eroded the
Doctor-Patient Relationship .......................................................................................371
Five days, no food, and a ton of water should do it.
That was a weaponised protein by the way.
badprotein.substack.com/p/parsimony
badprotein.substack.com/p/friends
badprotein.substack.com/p/orientation
If it is gene based how can you get rid of the jabs based materials?
this was shown in one window and suppressed in another. repost.
Spike toxicities
1. RBD: Presents spike apex for antibodies; persistent expression binds ACE2, downregulating it and driving hyper-inflammation.
2. Furin Cleavage Site: Sheds soluble S1 that circulates systemically and crosses the blood-brain barrier.
3. S2’ Cleavage / Fusion: Exposes fusion peptide, triggering syncytia formation and cell apoptosis.
4. NTD Motifs: Binds DC-SIGN/L-SIGN to enter immune cells, disrupting macrophages and provoking cytokine cascades.
5. NRP1 Sequence: Exposed C-terminal motif binds NRP1, facilitating neuro-invasion and CNS signaling disruption.
6. T-Cell Mismatch: Oversized 1,273-aa sequence increases cellular stress and protein misfolding risk.
7. Molecular Mimicry: Short identical peptides match human proteins (e.g., myelin basic protein), risking autoimmunity.
8. Superantigen-Like Motif: Cross-links TCRs with MHC II, driving massive T-cell activation and inflammation.
9. Fibrinogen-Binding: Hydrophobic domains bind fibrinogen, inducing plasmin-resistant amyloid micro-clots.
10. Dark ORFs: Codon optimization increases alternative ORFs, producing truncated or frame-shifted proteins.
11. NLS Motifs: Functional nuclear localization signals can translocate spike into the nucleus, interfering with DNA repair.
12. GRP78 Binding: Overwhelms ER chaperones, induces ER stress, and promotes cellular senescence.
13. Mitochondrial Targeting: Interacts with VDAC1, disrupting membrane potential and raising ROS levels.
14. Broad-Spectrum S2: Soluble S2 acts as a decoy and inserts into neighboring membranes, altering cell signaling.
15. Free S1 BBB Feature: Degrades tight junctions, breaches the blood-brain barrier, and triggers neuro-inflammation.
16. 2P Stabilization: Locks spike in pre-fusion shape, hindering proteolytic breakdown and extending tissue half-life.
17. Cryptic Epitope Masking: Glycan shifts mask neutralizing sites, exposing cryptic epitopes and increasing ADE risk.
18. CD147 Binding: Causes erythrocyte aggregation and platelet activation, promoting micro-vascular sludging.
19. TLR4 Hyper-Activation: Hydrophobic region hyper-activates TLR4, provoking a MyD88-dependent cytokine surge.
20. Complement Activation: Binds Factor H to disable complement regulation and trigger endothelial/platelet damage.
21. G-Quadruplex Motifs: G-rich sequences sequester host binding proteins, disrupting post-transcriptional gene regulation.
22. LINE-1 Activation: Intracellular stress activates LINE-1, potentially enabling reverse-transcription and genomic integration.
23. Prion-Like GXXXG: Nucleates misfolding of host proteins like alpha-synuclein and amyloid-beta.
24. nAChR Antagonist: Insertion homologous to neurotoxins impairs the cholinergic anti-inflammatory pathway.
25. IgG4 Class Switch: Chronic exposure drives IgG4 switching and immune tolerance, reducing antiviral responses.
26. HLA-G Induction: Upregulates HLA-G, creating local immune privilege that shields cells from NK and CTL clearance.
27. Integrin RGD-like: Binds integrins, activates Src pathways, and loosens endothelial junctions causing leakage.
28. PPAR-γ Suppression: Internalized spike downregulates PPAR-γ, promoting endothelial fibrosis and inflammation.
29. SQSTM1/p62 Domain: Binds p62 to stall autophagy, accumulating misfolded waste and triggering senescence.
30. USP14 Deactivation: Inhibits USP14 to jam proteasomal clearance and precipitate apoptosis.
31. Cofilin-1 Activation: Hyper-activates Cofilin-1, severing actin and forming tunneling nanotubes for cargo spread.
32. MLCK Up-regulation: Contracts endothelial cytoskeleton and opens intercellular gaps, driving edema.
33. ENaC Homology: Mimics ENaC activation sites, impairing sodium and fluid clearance across barriers.
34. TMEM16F Interactivity: Over-activates TMEM16F, causing calcium influx and flagging cells for macrophage clearance.
35. AT1R Hyper-Sensitizer: Enhances AT1R signaling, amplifying vasoconstriction, oxidative stress, and fibrosis.
36. LHR Cross-Reactive Core: Resembles LHR binding loops, risking antibody cross-reaction with reproductive receptors.
37. MMP-9 Induction: Triggers heavy MMP-9 release, degrading extracellular matrix and basement membranes.
38. TIMP-3 Suppression: Removes inhibition of matrix metalloproteinases, enabling runaway tissue degradation.
39. DNMT1 Hyper-Stimulation: Causes epigenetic hyper-methylation and silencing of protective genes.
40. HDAC Destabilizer: Destabilizes regulatory complexes, perturbing chromatin acetylation balance.
41. VMAT2 Interactivity: Binds VMAT2 in neuroendocrine cells, causing synaptic signaling imbalances.
42. MAO-B Modulator: Upregulates MAO-B in glia, increasing dopamine breakdown and oxidative stress.
43. Prestin Homology: Resembles Prestin, risking cross-reaction with outer hair cells and causing tinnitus.
44. Otolin-1 Degradation: Triggers matrix-degrading enzymes to break down Otolin-1 and dislodge otoconia (BPPV).
45. SIRT1 Suppressor: Blocks SIRT1 activity, accelerating cellular senescence and pro-inflammatory states.
46. p53 Sequestration: Sequestrates p53 in the cytoplasm, impairing tumor-suppressor functions.
47. LYVE-1 Binding: Binds LYVE-1 on lymphatic endothelium, promoting inflammation and slowing drainage.
48. S1PR1 Internalization: Downregulates S1PR1 on lymphocytes, trapping T-cells in lymphoid organs (lymphopenia).
49. Thrombomodulin Inhibitor: Binds TM's lectin-like domain, shifting vasculature toward a pro-thrombotic state.
50. Protein C Shielding: Interferes with Protein C activation, reducing anticoagulant protection.
51. Pericyte Detachment: Binds ACE2 on pericytes, triggering detachment, leakage, and endothelial dysfunction.
52. Caveolin-1 Portal: Triggers Caveolin-1 transcytosis, allowing S1 to cross barriers into sub-endothelial tissues.
53. MMP-2 Dissolver: Upregulates MMP-2 to degrade claudin-5 and occludin, compromising the blood-brain barrier.
54. Mac-1 Alarm Trigger: Binds Mac-1 on microglia, shifting them to a neurotoxic M1 phenotype.
55. FDC Trapping Loop: Glycosylated S1 is trapped on FDCs for months, driving continuous B-cell activation.
56. Exosome Packaging: Endothelial cells package S1 into exosomes that deliver cargo to distant organs.
57. Glycophorin A Clumping: Binds GPA on RBCs, promoting rouleaux formation and increased blood viscosity.
58. CD36 Overdrive: Overloads CD36 macrophages with micro-clots, converting them into inflammatory foam cells.
59. Pericyte Spasm Motif: Triggers calcium spikes and contraction in cardiac pericytes, inducing focal ischemia.
60. Desmin Disruption: Disrupts desmin scaffolding in muscle networks, compromising structural integrity.
61. Cross-Presentation Crossroads: Bystander cells endocytose shed S1, causing cytotoxic T-cells to target innocent cells.
62. Endothelial Auto-Aggression: Widespread S1 display draws CD8+ attacks, producing vasculitis and micro-thrombosis.
63. Perforin Hole-Punch Effect: Perforin spills outward at synapses, creating non-specific collateral bystander lysis.
64. Granzyme B Dissolution: Degrades fibronectin and laminin, destabilizing capillary basement membranes.
65. Cardiomyocyte Trap: Recruits T-cells that destroy non-regenerative cardiomyocytes, leaving permanent scars.
66. Fas/FasL Amplification: Upregulates Fas on neighboring cardiomyocytes, enabling bystander apoptosis.
67. IFN-γ Gate-Opening: Disrupted VE-cadherin alignment opens endothelial junctions, permitting hemorrhage.
68. TNF-α E-Selectin Overdrive: Causes leukocyte-platelet aggregates that occlude micro-capillaries.
69. Oligoclonal T-Cell Stasis: Drives narrow T-cell expansion, transiently impairing responses to other pathogens.
70. PD-1/CTLA-4 Exhaustion: Enforces immune cell exhaustion, locking them into a hyporesponsive state.
71. Heparan Sulfate Binding: Binds cell-surface heparan sulfates, enhancing tissue retention and broad tropism.
72. HSP Chaperone Hijack: Recruits heat-shock proteins, amplifying proteostasis stress across cells.
73. ER-Mitochondria Perturbation: Disruption at junction sites impairs calcium signaling and bioenergetic coupling.
74. Interferon Amplifier: Drives a self-sustaining interferon loop, maintaining chronic tissue inflammation.
75. MicroRNA Sponge: Sequesters host microRNAs, dysregulating post-transcriptional gene control.
76. Alternative Splicing Interference: Sequesters splicing factors to produce aberrant, tissue-impairing isoforms.
77. Lipid Raft Sequestration: Inserts into lipid rafts, chronically activating pro-inflammatory kinase cascades.
78. PF4 Mimicry: Short peptides mimic PF4 epitopes, potentially promoting anti-PF4 antibody formation.
79. Complement Regulator Mimicry: Resembles host regulators, confusing complement targeting and deposition.
80. FDC Depot Stabilizer: Glycan features favor long-term retention, creating persistent germinal-center activity.
81. Glycocalyx Sensor Disruption: Strips endothelial glycocalyx, impairing shear-stress sensing and flow.
82. NLRP3 Priming Patch: Primes and activates NLRP3 in macrophages, driving IL-1β and pyroptotic inflammation.
83. Platelet Integrin Trigger: Directly engages platelet alpha-IIb beta-3, lowering thresholds for aggregation.
84. Extracellular Vesicle Display: Increases circulatory half-life and tissue delivery of antigenic cargo.
85. eNOS Uncoupling: Oxidative stress uncouples eNOS, reducing NO availability and promoting vasoconstriction.
86. Glycosaminoglycan Remodeling: Upregulates heparanase and hyaluronidase, increasing tissue permeability.
87. Neoepitope Exposure: Febrile conditions reveal hidden neoepitopes, broadening autoantibody targets.
88. mtDNA Release: Damaged mitochondria release mtDNA that activates cGAS-STING pathways.
89. SASP Inducer: Drives endothelial cells into senescence, producing factors that perpetuate inflammation.
You get rid of them wih FIRE
https://badprotein.substack.com/p/the-fastening
Not jabbed. Question is even if 5day fasting doing and resetting completed what happens if reinfection occurs (if a person lives in highly jabbed country) and cycle of symptoms recur. Is this then a 5 day fast repeat.
Thanks for the wonderful info on fasting. 67+ old not jabbed.
The nice thing about planned fasting is that you can schedule it.
So you can do it every decade
every year
every month
I fasted for 10 days before and learned that 5 days was correct. I kept going with the fast because i could - but it was 2 years before my stomach digested properly again. I ate too much of myself, but passing on the info to others makes it worth gaining in the first place.
So really fasting shouldn't be seen as an intervention, so much as periodic preventative maintenance. Lots of cultures preserve the basic knowlege - some religions do it annually. No doubt there is a Californian that eats 3 days on and 3 days off lol. It depends of course on the person, and constituency.
The Sars-Cov2 VIRUS was equipped with 2 nasty proteases that go around the infected cell and start chopping up host proteins. They do not get a lot of attention - but they were nasty. My hypothesis is autoimmunity - not from what the virus made, but from what it destroyed - self.
Because the virus was engineered with the furin cleavage site, and gained entry with ACE2 - it was a bat poison that was given a backstage pass to every cell in the human body - when normally a bat virus would be locked out. If they didn't do the gain of function then Sars-Cov2 would have been less than a cold. But they did, and whatever cryptic layers they engineered into it will unfold in the host. But it is a damage that evenually get's stopped by the normal immune system. A flooded basement might be ruined, but it will be dry in beween floods. There can be damage - but it's not an ongoing damage in general. So a fast is likely to not do much unless you suspect your immune system picked up immunity to the foreign bug, AND yourself.
the case of vaccination is way worse - there are many more things wrong about the LNP transfection platforms. LNP damages, biodistribution from LNP size variation and vroman effect making spike where viruses never reach. for time way longer than a virus acts.
in the case of infection the virus makes more copies of itself - and then tries to make you sneeze - it needs all the arms and legs it made for itself in your cell when it's mother virus invaded and started using it for parts.
in the case of the vaccine, it was not a case of a virus making children with arms and legs and spike proteins as per the virus recipe. the LNP was just a work order to make thumbs. a trillion LNPs, with each mRNA fragment making 1000-5000 copies of thumbs (spike protein only - no other virus parts).
so the vaccine will fill you up wth 1000x too much antigen - enough to flash-bang the natural immune system to making the same knee jerk reaction for every future infection....
thumbs EVERYWHERE - in the brains, ovaries, adrenal glands..
so vaccination problems need the 'cleanup' more than infection.
infection is the single best vaccination and offers the most immunity - not just a wanted poster for Hitler showing only a short mustache
but people got covid 6 times so that tells you that vaccines are literally useless. Omicron IS the airborne vaccine - avoid it like you avoid vaccination. but of you catch Omicron again, your vaccine is up to date.
Where can I send you a document that outlines what happened; intent and how? With documents. Some aspects of CV are still not in the public. DM me.