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SCIENTISTS HAVE CRACKED PART OF THE BRAIN’S AGING CODE Your brain’s protein-making system runs smoothly when young, matching mRNA “manuals” to finished proteins. With age, that sync breaks, older cells pile up manuals while production lines stall. In fish brains, scientists found the biggest slowdowns in positively charged proteins,...

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Mario Nawfal

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This is how DNA turns raw data into functional proteins - the building blocks of all your cells. This system requires a minimum of 3 key players working together: DNA: the master blueprint with the instructions RNA Polymerase: reads the DNA and makes a temporary copy called mRNA which carries the instructions to the Ribosome for how to create the Protein Ribosome: the tiny factory that reads the mRNA and strings amino acids together in a specific sequence to create a protein Without all three molecules working together, Proteins cannot be created, cells don't function, and Life ends. Everything needs to fit together, precisely & perfectly, or it all falls apart. In other words: this system cannot evolve, one step at a time. DNA relies other machines made of proteins to create those very proteins - but those proteins can't be made without the information in the DNA. And on top of that, this whole system relies on OTHER systems! You need other things like ATP Synthase that makes energy to power everything, tRNA to carry the amino acids to the Ribosome, other helper proteins, processing enzymes, etc. It's an extremely complex, interdependent network of parts & systems that all rely on each other. The cell is an astounding level of complexity that surpasses anything in human engineering. It's obvious this is intelligently designed. To deny that is absurd.
2:15

This is how DNA turns raw data into functional proteins - the building blocks of all your cells. This system requires a minimum of 3 key players working together: DNA: the master blueprint with the instructions RNA Polymerase: reads the DNA and makes a temporary copy called mRNA which carries the instructions to the Ribosome for how to create the Protein Ribosome: the tiny factory that reads the mRNA and strings amino acids together in a specific sequence to create a protein Without all three molecules working together, Proteins cannot be created, cells don't function, and Life ends. Everything needs to fit together, precisely & perfectly, or it all falls apart. In other words: this system cannot evolve, one step at a time. DNA relies other machines made of proteins to create those very proteins - but those proteins can't be made without the information in the DNA. And on top of that, this whole system relies on OTHER systems! You need other things like ATP Synthase that makes energy to power everything, tRNA to carry the amino acids to the Ribosome, other helper proteins, processing enzymes, etc. It's an extremely complex, interdependent network of parts & systems that all rely on each other. The cell is an astounding level of complexity that surpasses anything in human engineering. It's obvious this is intelligently designed. To deny that is absurd.

Divinely Designed

22,903 Aufrufe • vor 7 Monaten

Most people don’t truly understand how mRNA vaccines work. Unlike traditional vaccines, where a factory produces the antigen and injects it into the body, mRNA vaccines turn YOUR OWN CELLS into the factory. Here’s how it works: Inside every one of your cells, there are ribosomes—tiny protein-making machines. Normally, these ribosomes get instructions from your cell’s nucleus (the brain of the cell) to produce proteins that build muscle, fight infections, and keep your body functioning. mRNA vaccines hijack this natural process by delivering a blueprint that instructs your ribosomes to produce a specific protein—like the spike protein of a virus. Your immune system then recognizes this protein as foreign, triggering a defense response and preparing your body to fight off future infections. Why does this matter? 1️⃣ Faster production – No need for external manufacturing of viral proteins, cutting vaccine development time. 2️⃣ Adaptability – The technology can be rapidly adjusted for new viruses and mutations. 3️⃣ No live virus – Unlike traditional vaccines, mRNA vaccines don’t use weakened or dead viruses, reducing risk. But here’s the big question: Are we playing with fire, or is this the future of medicine? We’re bypassing nature’s traditional immune response by directly programming our cells to make viral proteins. Dr. Mink Chawla and I break it all down in this episode. WATCH HERE:
0:48

Most people don’t truly understand how mRNA vaccines work. Unlike traditional vaccines, where a factory produces the antigen and injects it into the body, mRNA vaccines turn YOUR OWN CELLS into the factory. Here’s how it works: Inside every one of your cells, there are ribosomes—tiny protein-making machines. Normally, these ribosomes get instructions from your cell’s nucleus (the brain of the cell) to produce proteins that build muscle, fight infections, and keep your body functioning. mRNA vaccines hijack this natural process by delivering a blueprint that instructs your ribosomes to produce a specific protein—like the spike protein of a virus. Your immune system then recognizes this protein as foreign, triggering a defense response and preparing your body to fight off future infections. Why does this matter? 1️⃣ Faster production – No need for external manufacturing of viral proteins, cutting vaccine development time. 2️⃣ Adaptability – The technology can be rapidly adjusted for new viruses and mutations. 3️⃣ No live virus – Unlike traditional vaccines, mRNA vaccines don’t use weakened or dead viruses, reducing risk. But here’s the big question: Are we playing with fire, or is this the future of medicine? We’re bypassing nature’s traditional immune response by directly programming our cells to make viral proteins. Dr. Mink Chawla and I break it all down in this episode. WATCH HERE:

Gary Brecka

51,737 Aufrufe • vor 1 Jahr

Proof that Life is Intelligently Designed: Proteins. They do everything in your cells that keeps you alive. These microscopic molecules must have been created. Here is why: Proteins are the building blocks of all the little nano-machines that make up your cells. They do all the major work in your body - from creating energy to recycling waste. Proteins are made from amino acids connected into a specific sequence and then folded into a functional shape. You can think of a protein like a paragraph, and amino acids as the individual letters that spell out the words. Here is where it gets interesting... There are just 20 amino acids used in all of Life. Just 20 amino acids. Responsible for ~200 million unique proteins making up tens of thousands of cell types across Life. And scientists are constantly finding new ones. Scientists categorize proteins into Families. Protein Families are groups of proteins that share amino acid sequence similarities. There are ~22,000 Protein Families. Here's the part that screams they are designed... Protein Families have no evolutionary history. Even evolutionist scientists agree - they are absolutely unique. It's been said that proteins are like stars in a galaxy, and families are like galaxies, with vast empty space between them. Evolution is supposed to build by tweaking things that already exist. But no evolutionary history connects fundamentally distinct protein families. Experiments have been done to intentionally evolve one protein family into another. They fail every time. One protein family cannot be evolved into another. They cannot arise through evolution. But the math really makes it impossible... The odds of evolution finding even a single functional protein family is 1 chance in 10^77 possible amino acid sequences. That's a 1 with 77 zeroes. The odds of evolution finding 22,000 distinct protein families? Roughly 1 chance in 10^1,694,000. You don't need to be a mathematician to understand that this is impossible. Evolution works by random mutations tweaking what's already there. But protein families can't evolve from one another. And the math makes it absolutely absurd to believe. Monkeys banging on keyboards will never type out Shakespeare. And random mutations in sequences of amino acids could never create a single functional protein family. There is only one thing we know of that creates functionally specified sequences: Intelligence. Now here is the final cherry on top: Proteins are built by other proteins, assembled into a complex machine to do a job in cells. The assembly instructions for those proteins and the machines are found in DNA. But DNA requires protein machines for replication & repair. So DNA is required to make Proteins... ...but Proteins are required to make DNA *and* more Proteins. You can't have one without the other. They rely on each other. Which means one couldn't have evolved and then waited for the other. They couldn't do anything without each other. They had to be created at the same time to function together. Life was Divinely Designed. Proteins prove it.
0:38

Proof that Life is Intelligently Designed: Proteins. They do everything in your cells that keeps you alive. These microscopic molecules must have been created. Here is why: Proteins are the building blocks of all the little nano-machines that make up your cells. They do all the major work in your body - from creating energy to recycling waste. Proteins are made from amino acids connected into a specific sequence and then folded into a functional shape. You can think of a protein like a paragraph, and amino acids as the individual letters that spell out the words. Here is where it gets interesting... There are just 20 amino acids used in all of Life. Just 20 amino acids. Responsible for ~200 million unique proteins making up tens of thousands of cell types across Life. And scientists are constantly finding new ones. Scientists categorize proteins into Families. Protein Families are groups of proteins that share amino acid sequence similarities. There are ~22,000 Protein Families. Here's the part that screams they are designed... Protein Families have no evolutionary history. Even evolutionist scientists agree - they are absolutely unique. It's been said that proteins are like stars in a galaxy, and families are like galaxies, with vast empty space between them. Evolution is supposed to build by tweaking things that already exist. But no evolutionary history connects fundamentally distinct protein families. Experiments have been done to intentionally evolve one protein family into another. They fail every time. One protein family cannot be evolved into another. They cannot arise through evolution. But the math really makes it impossible... The odds of evolution finding even a single functional protein family is 1 chance in 10^77 possible amino acid sequences. That's a 1 with 77 zeroes. The odds of evolution finding 22,000 distinct protein families? Roughly 1 chance in 10^1,694,000. You don't need to be a mathematician to understand that this is impossible. Evolution works by random mutations tweaking what's already there. But protein families can't evolve from one another. And the math makes it absolutely absurd to believe. Monkeys banging on keyboards will never type out Shakespeare. And random mutations in sequences of amino acids could never create a single functional protein family. There is only one thing we know of that creates functionally specified sequences: Intelligence. Now here is the final cherry on top: Proteins are built by other proteins, assembled into a complex machine to do a job in cells. The assembly instructions for those proteins and the machines are found in DNA. But DNA requires protein machines for replication & repair. So DNA is required to make Proteins... ...but Proteins are required to make DNA *and* more Proteins. You can't have one without the other. They rely on each other. Which means one couldn't have evolved and then waited for the other. They couldn't do anything without each other. They had to be created at the same time to function together. Life was Divinely Designed. Proteins prove it.

Divinely Designed

18,886 Aufrufe • vor 1 Monat

It’s embarrassing to watch the TGA tie itself up in knots and contradict itself over the safety of the vaccine. The mRNA vaccine is designed to attack your own cells because the antigen sits on the cell membrane. The T-cell which responds to the vaccine antigen can’t separate your cell from the spike protein. It kills both and the TGA has already admitted as much in the past conceding myocarditis is an autoimmune response. The spike proteins are not rapidly degraded as numerous studies have shown they last in the body for up to 60 days. But more importantly the mRNA is designed to last much longer and produce more proteins. This means the body produces a much larger concentration of the toxic spike protein than what the virus would have delivered. And I quote from one study: “Later studies documented similar effects for 5-methylcytidine and 2-thiouridine and observed that modified mRNAs produced 10- to 100-fold more protein compared with unmodified mRNAs. Recently, N1-methylpseudouridine (m1Ψ), the modification used in the current mRNA SARS-CoV-2 vaccines, was found to possess superior characteristics to Ψ; m1Ψ elicited less immunogenicity and increased protein production by more than an order of magnitude relative to Ψ.” And another on the Poly-A tail increases the duration. “Whether for the mRNA vaccine from Pfizer/BioNtech® laboratories or that of Moderna®, the two mRNA sequences end in a Poly(A) tail. The purpose of this addition is to increase the stability of the mRNA in biological medium and also to allow the recruitment of the ribosome, in order to initiate an efficient translation. After translation, the mRNA can be reused several times, but when this happens, it also loses part of the Adenines of its Poly(A) tail, as enzymatic degradation begins there, which only ensures a transient protection against this degradation. When this tail is too degraded, the mRNA is no longer functional and is destroyed. The poly(A) tail stabilizes mRNA and boosts protein translation, and the length of the poly(A) tail is proportional to translation efficiency. It is a critical factor in determining the longevity of mRNA molecules.” Long story short - the TGA continues to lie. Quotes from: #auspol
2:19

It’s embarrassing to watch the TGA tie itself up in knots and contradict itself over the safety of the vaccine. The mRNA vaccine is designed to attack your own cells because the antigen sits on the cell membrane. The T-cell which responds to the vaccine antigen can’t separate your cell from the spike protein. It kills both and the TGA has already admitted as much in the past conceding myocarditis is an autoimmune response. The spike proteins are not rapidly degraded as numerous studies have shown they last in the body for up to 60 days. But more importantly the mRNA is designed to last much longer and produce more proteins. This means the body produces a much larger concentration of the toxic spike protein than what the virus would have delivered. And I quote from one study: “Later studies documented similar effects for 5-methylcytidine and 2-thiouridine and observed that modified mRNAs produced 10- to 100-fold more protein compared with unmodified mRNAs. Recently, N1-methylpseudouridine (m1Ψ), the modification used in the current mRNA SARS-CoV-2 vaccines, was found to possess superior characteristics to Ψ; m1Ψ elicited less immunogenicity and increased protein production by more than an order of magnitude relative to Ψ.” And another on the Poly-A tail increases the duration. “Whether for the mRNA vaccine from Pfizer/BioNtech® laboratories or that of Moderna®, the two mRNA sequences end in a Poly(A) tail. The purpose of this addition is to increase the stability of the mRNA in biological medium and also to allow the recruitment of the ribosome, in order to initiate an efficient translation. After translation, the mRNA can be reused several times, but when this happens, it also loses part of the Adenines of its Poly(A) tail, as enzymatic degradation begins there, which only ensures a transient protection against this degradation. When this tail is too degraded, the mRNA is no longer functional and is destroyed. The poly(A) tail stabilizes mRNA and boosts protein translation, and the length of the poly(A) tail is proportional to translation efficiency. It is a critical factor in determining the longevity of mRNA molecules.” Long story short - the TGA continues to lie. Quotes from: #auspol

Gerard Rennick

62,548 Aufrufe • vor 1 Jahr

"Frankenstein Proteins" The technology underpinning every mRNA 'vaccine' is creating strange "Frankenstein proteins" in the body and "no one knows what those proteins are doing". Pseudouridine was given a Nobel Prize before peer reviewed research from Cambridge found strange proteins circulating in the body of the vaccinated. Dr Ryan Cole discusses with Dr Kelly Victory: "This means is you're also coding for Frankenstein proteins, which may be functional, which may be triggering autoimmune reactions." "You're making proteins in addition to, you know the supposed spike protein, you're making unintended but potentially consequential proteins, that can cause the immune system also to go haywire." "So this was found out a couple years into the rollout of the shots and these very esteemed researchers said 'Houston we have a problem'. " Yet Paul Offit and the AAP wants this injected into healthy 2 year olds and children. Who has the moral high ground here?
2:34

"Frankenstein Proteins" The technology underpinning every mRNA 'vaccine' is creating strange "Frankenstein proteins" in the body and "no one knows what those proteins are doing". Pseudouridine was given a Nobel Prize before peer reviewed research from Cambridge found strange proteins circulating in the body of the vaccinated. Dr Ryan Cole discusses with Dr Kelly Victory: "This means is you're also coding for Frankenstein proteins, which may be functional, which may be triggering autoimmune reactions." "You're making proteins in addition to, you know the supposed spike protein, you're making unintended but potentially consequential proteins, that can cause the immune system also to go haywire." "So this was found out a couple years into the rollout of the shots and these very esteemed researchers said 'Houston we have a problem'. " Yet Paul Offit and the AAP wants this injected into healthy 2 year olds and children. Who has the moral high ground here?

Humanspective

15,413 Aufrufe • vor 11 Monaten

Friedberg: New study shows enzyme reverses skin age from 70+ years to 31 Chamath: That’s a $2T market. Did Scientists Just Discover How to Reverse Skin Aging!? “CML is kind of the predominant molecule that gets formed in this extracellular matrix that's driving aging, and nothing breaks it down. So these scientists set out to try and create an enzyme, an enzyme is a protein that breaks something down, that can break down CML. And so these guys kind of went out and they took the target, which is CML, and tried to figure out, ‘Okay, how do we actually degrade CML, clear that extracellular matrix, and reverse aging?’ They started to test it on the proteins that we would find in our body, casein, collagen, retinal proteins, which are in your eye, hemoglobin, and they were able to get rid of 52 to 97% of the CML, just degrade it away. And then they found several sites where they were able to degrade over 90%. And then they took actual human skin from elderly patients that had donated their skin, and they put this enzyme onto that skin, and they were able to eliminate 55% of the CML on the skin, basically reverse the skin's age down to the age of a 31-year-old, this is from greater than 70-year-old patients, just by putting this enzyme on the skin. And so it's kind of a groundbreaking demonstration of combination of AlphaFold, what's called directed evolution, where you change the order of the DNA that changes the structure of the protein to test different proteins, do high throughput screening, and ultimately make a novel protein that doesn't exist in nature today that can do something pretty profound for human health.” Chamath: “It will be a trillion-dollar market. If you can create a cream…” Friedberg: “I mean, dude, if you could put this enzyme literally on your skin and have it absorb in…” Chamath: “Game over. That alone is $2 trillion.”
1:42

Friedberg: New study shows enzyme reverses skin age from 70+ years to 31 Chamath: That’s a $2T market. Did Scientists Just Discover How to Reverse Skin Aging!? “CML is kind of the predominant molecule that gets formed in this extracellular matrix that's driving aging, and nothing breaks it down. So these scientists set out to try and create an enzyme, an enzyme is a protein that breaks something down, that can break down CML. And so these guys kind of went out and they took the target, which is CML, and tried to figure out, ‘Okay, how do we actually degrade CML, clear that extracellular matrix, and reverse aging?’ They started to test it on the proteins that we would find in our body, casein, collagen, retinal proteins, which are in your eye, hemoglobin, and they were able to get rid of 52 to 97% of the CML, just degrade it away. And then they found several sites where they were able to degrade over 90%. And then they took actual human skin from elderly patients that had donated their skin, and they put this enzyme onto that skin, and they were able to eliminate 55% of the CML on the skin, basically reverse the skin's age down to the age of a 31-year-old, this is from greater than 70-year-old patients, just by putting this enzyme on the skin. And so it's kind of a groundbreaking demonstration of combination of AlphaFold, what's called directed evolution, where you change the order of the DNA that changes the structure of the protein to test different proteins, do high throughput screening, and ultimately make a novel protein that doesn't exist in nature today that can do something pretty profound for human health.” Chamath: “It will be a trillion-dollar market. If you can create a cream…” Friedberg: “I mean, dude, if you could put this enzyme literally on your skin and have it absorb in…” Chamath: “Game over. That alone is $2 trillion.”

The All-In Podcast

2,971,836 Aufrufe • vor 1 Monat

This is how DNA turns coded information into functional proteins - the building blocks of the nanomachines that keep the cells in your body alive. This complex process highlights the sophisticated interconnected systems of Life which must all exist together from the beginning, or Life doesn't happen. First, an RNA molecule is copied from a short segment of DNA. Without the specifically ordered DNA information, RNA cannot form, proteins cannot be built, cells stop working, and life ceases to exist. Life is information first. Once the RNA Molecule is created, it gets ejected from the Polymerase where it was built, and it travels through a complex molecular machine called a Nuclear Pore Complex (NPC), which is an information recognition device that controls the flow of information in and out of a cell's nucleus. The NPC is highly complex - composed of about 500-1,000 protein subunits, derived from a set of about 35 distinct proteins. Without this molecular machine, there is no regulation for what goes in and out of the cell's nucleus, which would lead to catastrophic death for the cell. It must exist for cells to exist. Once the RNA Molecule passes through the NPC, it travels to the Ribosome, a 2-part chemical factory which reads the information on RNA and uses it to construct functional proteins using a specifically sequenced chain of amino acids. Once complete, this protein will then be sent to the section of the cell it belongs to integrate into another molecular machine and do its job. The Ribosome is another highly complex molecular machine - consisting of between 56-80 proteins. Without this molecular machines, proteins cannot be built. Proteins are the building blocks of every cell in every organism on Earth. Without Ribosomes, Life doesn't exist. If you're paying attention, you'll start to realize that Life relies on a highly sophisticated interdependent network of complex machines, which all rely on each other for the function of the system. DNA requires the cell for stability, but the cell requires the proteins for its structure and function, but those proteins require DNA and RNA to be built - it's a circle of necessary interdependence. Systems like this cannot be built by evolutionary processes, which requires that each piece of the process is built by gradual incremental means over lots of time. Without all the pieces there, from the beginning, none of it works. There is only one known source of complex & interdependent informational systems like those we find in life: and that is from Intelligence. Molecular Biology is the best and most obvious evidence of the Intelligent Design in Life.
0:55

This is how DNA turns coded information into functional proteins - the building blocks of the nanomachines that keep the cells in your body alive. This complex process highlights the sophisticated interconnected systems of Life which must all exist together from the beginning, or Life doesn't happen. First, an RNA molecule is copied from a short segment of DNA. Without the specifically ordered DNA information, RNA cannot form, proteins cannot be built, cells stop working, and life ceases to exist. Life is information first. Once the RNA Molecule is created, it gets ejected from the Polymerase where it was built, and it travels through a complex molecular machine called a Nuclear Pore Complex (NPC), which is an information recognition device that controls the flow of information in and out of a cell's nucleus. The NPC is highly complex - composed of about 500-1,000 protein subunits, derived from a set of about 35 distinct proteins. Without this molecular machine, there is no regulation for what goes in and out of the cell's nucleus, which would lead to catastrophic death for the cell. It must exist for cells to exist. Once the RNA Molecule passes through the NPC, it travels to the Ribosome, a 2-part chemical factory which reads the information on RNA and uses it to construct functional proteins using a specifically sequenced chain of amino acids. Once complete, this protein will then be sent to the section of the cell it belongs to integrate into another molecular machine and do its job. The Ribosome is another highly complex molecular machine - consisting of between 56-80 proteins. Without this molecular machines, proteins cannot be built. Proteins are the building blocks of every cell in every organism on Earth. Without Ribosomes, Life doesn't exist. If you're paying attention, you'll start to realize that Life relies on a highly sophisticated interdependent network of complex machines, which all rely on each other for the function of the system. DNA requires the cell for stability, but the cell requires the proteins for its structure and function, but those proteins require DNA and RNA to be built - it's a circle of necessary interdependence. Systems like this cannot be built by evolutionary processes, which requires that each piece of the process is built by gradual incremental means over lots of time. Without all the pieces there, from the beginning, none of it works. There is only one known source of complex & interdependent informational systems like those we find in life: and that is from Intelligence. Molecular Biology is the best and most obvious evidence of the Intelligent Design in Life.

Divinely Designed

62,517 Aufrufe • vor 7 Monaten

New findings from Dr. Peter McCullough and a German research lab confirm that Pfizer and Moderna mRNA vaccines leave behind synthetic spike protein in the body for at least 3.2 years post-injection. These proteins circulate in the bloodstream and embed in tissues, with no known human enzymes capable of breaking them down. Key Revelations: - Pseudouridinated mRNA does not degrade naturally, leading to prolonged spike protein production. - Cancer trends shifting—2023 data shows rising breast and prostate cancers, while overall rates remain stable. - 2021 global mortality was among the worst in history, raising urgent questions about long-term vaccine effects. Potential Solutions? Natural enzymes like nattokinase, bromelain, serrapeptase, and lumbrokinase show promise in breaking down spike protein—but public awareness is critical. Why This Matters: If mRNA and spike protein persist for years, the long-term health consequences could be devastating. The medical establishment must address this—before it’s too late.
1:21

New findings from Dr. Peter McCullough and a German research lab confirm that Pfizer and Moderna mRNA vaccines leave behind synthetic spike protein in the body for at least 3.2 years post-injection. These proteins circulate in the bloodstream and embed in tissues, with no known human enzymes capable of breaking them down. Key Revelations: - Pseudouridinated mRNA does not degrade naturally, leading to prolonged spike protein production. - Cancer trends shifting—2023 data shows rising breast and prostate cancers, while overall rates remain stable. - 2021 global mortality was among the worst in history, raising urgent questions about long-term vaccine effects. Potential Solutions? Natural enzymes like nattokinase, bromelain, serrapeptase, and lumbrokinase show promise in breaking down spike protein—but public awareness is critical. Why This Matters: If mRNA and spike protein persist for years, the long-term health consequences could be devastating. The medical establishment must address this—before it’s too late.

Camus

77,549 Aufrufe • vor 1 Jahr

🚨 SURGEON WARNS THE BIGGEST BREAKTHROUGH IN HUMAN HISTORY IS HAPPENING RIGHT NOW — “BIGGER THAN AI” A surgeon is going viral after claiming scientists may have already discovered a way to partially REVERSE aging at the DNA level… and he says the implications are bigger than AI, social media, smartphones, or even the internet itself. Dr. Buck Parker’s claim: “The fountain of youth has been discovered.” “This is bigger than the Industrial Revolution. Bigger than the advent of the internet. Bigger than Amazon, Apple, the iPhone, Google, social media… bigger than AI.” And according to Dr. Parker… it’s already happening RIGHT NOW. The core claim revolves around something called “Yamanaka factors,” proteins discovered by Nobel Prize-winning researcher Shinya Yamanaka that can reportedly reset damaged cells back to a younger biological state. According to Dr. Parker: • Scientists have reportedly reversed visible signs of aging in animals • Wrinkled skin in test subjects appeared to become youthful again • Researchers are now experimenting with literally “turning back” cellular age • Human trials are reportedly beginning • Some scientists now believe aging itself may simply be accumulated DNA damage His warning: “If you’ve been alive for the last 40 years… you’ve seen some wild sh*t happen. It’s about to get more wild.” If this became available tomorrow… would you actually take it? 📹: drbuckparker
5:18

🚨 SURGEON WARNS THE BIGGEST BREAKTHROUGH IN HUMAN HISTORY IS HAPPENING RIGHT NOW — “BIGGER THAN AI” A surgeon is going viral after claiming scientists may have already discovered a way to partially REVERSE aging at the DNA level… and he says the implications are bigger than AI, social media, smartphones, or even the internet itself. Dr. Buck Parker’s claim: “The fountain of youth has been discovered.” “This is bigger than the Industrial Revolution. Bigger than the advent of the internet. Bigger than Amazon, Apple, the iPhone, Google, social media… bigger than AI.” And according to Dr. Parker… it’s already happening RIGHT NOW. The core claim revolves around something called “Yamanaka factors,” proteins discovered by Nobel Prize-winning researcher Shinya Yamanaka that can reportedly reset damaged cells back to a younger biological state. According to Dr. Parker: • Scientists have reportedly reversed visible signs of aging in animals • Wrinkled skin in test subjects appeared to become youthful again • Researchers are now experimenting with literally “turning back” cellular age • Human trials are reportedly beginning • Some scientists now believe aging itself may simply be accumulated DNA damage His warning: “If you’ve been alive for the last 40 years… you’ve seen some wild sh*t happen. It’s about to get more wild.” If this became available tomorrow… would you actually take it? 📹: drbuckparker

HustleBitch

1,070,711 Aufrufe • vor 3 Monaten

DISTURBING: A new peer-reviewed study has blown apart everything we were told about mRNA injections, finding Pfizer’s genetic material in human placentas, blood, sperm, and even in unvaccinated pregnant women. The evidence is deeply worrisome, pointing to long term persistence, direct reproductive exposure and the very real possibility of shedding, something experts once insisted could not happen. Scientists found Pfizer mRNA in 88% of recently vaccinated pregnant women, including deep inside placental tissue. Every male donor who produced sperm carried vaccine mRNA in their sperm cells, and half still had it in seminal fluid months later. Most startling, half of the unvaccinated pregnant women tested positive, with mRNA appearing in both placenta and blood. The findings directly contradict the claim that the mRNA “stays in the arm,” and with the DOJ now trying to shut down Brook Jackson 💜's case against Pfizer, the stakes could not be higher. Watch ZeeeMediaOfficial's full report to understand why this disturbing discovery changes everything. 👇
10:23

DISTURBING: A new peer-reviewed study has blown apart everything we were told about mRNA injections, finding Pfizer’s genetic material in human placentas, blood, sperm, and even in unvaccinated pregnant women. The evidence is deeply worrisome, pointing to long term persistence, direct reproductive exposure and the very real possibility of shedding, something experts once insisted could not happen. Scientists found Pfizer mRNA in 88% of recently vaccinated pregnant women, including deep inside placental tissue. Every male donor who produced sperm carried vaccine mRNA in their sperm cells, and half still had it in seminal fluid months later. Most startling, half of the unvaccinated pregnant women tested positive, with mRNA appearing in both placenta and blood. The findings directly contradict the claim that the mRNA “stays in the arm,” and with the DOJ now trying to shut down Brook Jackson 💜's case against Pfizer, the stakes could not be higher. Watch ZeeeMediaOfficial's full report to understand why this disturbing discovery changes everything. 👇

The Vigilant Fox 🦊

100,597 Aufrufe • vor 8 Monaten

"The WHO Intends For ALL Vaccines On Earth To Be mRNA & Must Be Forbidden." Dr Sucharit Bhakdi "Every mRNA Injection Will Severely Change Your Brain, Damage Your Entire Body & Weaken Your Heart." The WHO Is A Private Club Financed By Germany & Bill Gates. They Must Be Stopped. mRNA Vaccines Do Not Save Lives...The Shots Contain A Killer Protein That Cannot Be Turned Off...It Is Not Safe By Design. The predominant vaccine platforms including messenger RNA (mRNA) are Pfizer, Moderna, AstraZeneca, Johnson & Johnson, Novavax & Zifi Vax – mRNA & viral vector vaccines involve the bodily synthesis of the S2 protein as the foundation of the immune response. Regardless of the vaccine platform used, circulating S2 protein is the detrimental agent through which mRNA vaccines cause biological harm. Here Is The 'How & Why' Of The S2 Protein Mechanism That Leads To Harm & Death: S2 protein initiates the breakdown & internalization of ACE2 receptors, which disrupts the renin–angiotensin system (RAS) & leads to increased inflammation, vasoconstriction & thrombosis. Further, S2 protein stimulates platelets & inflicts damage to the endothelium, which leads to arterial & venous thrombosis. Immune cells that have absorbed the lipid nanoparticles (LNPs) subsequently reintroduce them into the bloodstream with a higher number of exosomes carrying microRNAs & S2 protein, resulting in drastic inflammation. Long term immune surveillance is compromised by mRNA vaccines due to IRF7, IRF9, p53 & BRCA suppression. There is a causal link between mRNA vaccination & myocarditis, neurodegenerative disease, immune thrombocytopenia, Bell's palsy, liver disease, impaired adaptive immunity, impeded DNA damage response & tumorigenesis. Moreover, a recent study found that repeated vaccination with mRNA-based vaccines leads to the production of abnormally high concentrations of IgG4 antibodies. These antibodies fail to neutralize S2 protein, which has been shown to circulate for at least 700 days, causing immune suppression & promoting the development of autoimmune diseases including myocarditis. 👇Fatal mRNA Vaccine-Induced Myocarditis👇 👇Cardiac Arrest After mRNA Vaccination👇 👇DNA Fragments In mRNA Vaccines👇 Speaker: Dr Sucharit Bhakdi, Microbiologist Video: @freedom_knocks
2:19

"The WHO Intends For ALL Vaccines On Earth To Be mRNA & Must Be Forbidden." Dr Sucharit Bhakdi "Every mRNA Injection Will Severely Change Your Brain, Damage Your Entire Body & Weaken Your Heart." The WHO Is A Private Club Financed By Germany & Bill Gates. They Must Be Stopped. mRNA Vaccines Do Not Save Lives...The Shots Contain A Killer Protein That Cannot Be Turned Off...It Is Not Safe By Design. The predominant vaccine platforms including messenger RNA (mRNA) are Pfizer, Moderna, AstraZeneca, Johnson & Johnson, Novavax & Zifi Vax – mRNA & viral vector vaccines involve the bodily synthesis of the S2 protein as the foundation of the immune response. Regardless of the vaccine platform used, circulating S2 protein is the detrimental agent through which mRNA vaccines cause biological harm. Here Is The 'How & Why' Of The S2 Protein Mechanism That Leads To Harm & Death: S2 protein initiates the breakdown & internalization of ACE2 receptors, which disrupts the renin–angiotensin system (RAS) & leads to increased inflammation, vasoconstriction & thrombosis. Further, S2 protein stimulates platelets & inflicts damage to the endothelium, which leads to arterial & venous thrombosis. Immune cells that have absorbed the lipid nanoparticles (LNPs) subsequently reintroduce them into the bloodstream with a higher number of exosomes carrying microRNAs & S2 protein, resulting in drastic inflammation. Long term immune surveillance is compromised by mRNA vaccines due to IRF7, IRF9, p53 & BRCA suppression. There is a causal link between mRNA vaccination & myocarditis, neurodegenerative disease, immune thrombocytopenia, Bell's palsy, liver disease, impaired adaptive immunity, impeded DNA damage response & tumorigenesis. Moreover, a recent study found that repeated vaccination with mRNA-based vaccines leads to the production of abnormally high concentrations of IgG4 antibodies. These antibodies fail to neutralize S2 protein, which has been shown to circulate for at least 700 days, causing immune suppression & promoting the development of autoimmune diseases including myocarditis. 👇Fatal mRNA Vaccine-Induced Myocarditis👇 👇Cardiac Arrest After mRNA Vaccination👇 👇DNA Fragments In mRNA Vaccines👇 Speaker: Dr Sucharit Bhakdi, Microbiologist Video: @freedom_knocks

Valerie Anne Smith

16,998 Aufrufe • vor 1 Jahr

It's astounding. An entire system went down the road thinking low oxygen saturation was a death sentence. Remdesivir and Ventilators was the answer. In the bottom clip, a Doctor inside the medical system receiving massive incentives for ticking the "death from covid" box says - "Nothing Works" and that "There's no antiviral therapy". Doctors outside the system like sabine hazan md showed the complete opposite. Her clinical experience showed how quickly Ivermectin worked to arrest low Oxygen and how Fauci was able to point to "evidence" that it "didn't work". The system set up the Ivermectin and HCQ trials to fail using fundamental and critical dosing mistakes which the scientists running the clinical trials would have and should have known. Making the trials fail was essential to validating the EUA status of mRNA injections and supporting an incentivised medical system that chose kidney toxic Remdesivir treatments and Ventilators that were essentially the "death sentence" they blamed on covid.
3:41

It's astounding. An entire system went down the road thinking low oxygen saturation was a death sentence. Remdesivir and Ventilators was the answer. In the bottom clip, a Doctor inside the medical system receiving massive incentives for ticking the "death from covid" box says - "Nothing Works" and that "There's no antiviral therapy". Doctors outside the system like sabine hazan md showed the complete opposite. Her clinical experience showed how quickly Ivermectin worked to arrest low Oxygen and how Fauci was able to point to "evidence" that it "didn't work". The system set up the Ivermectin and HCQ trials to fail using fundamental and critical dosing mistakes which the scientists running the clinical trials would have and should have known. Making the trials fail was essential to validating the EUA status of mRNA injections and supporting an incentivised medical system that chose kidney toxic Remdesivir treatments and Ventilators that were essentially the "death sentence" they blamed on covid.

Humanspective

106,058 Aufrufe • vor 8 Monaten

This is how cells make energy - the production of ATP. All life requires ATP for energy. Without it, cells cannot function, and Life cannot survive. That means ATP Synthase is required from the very start of Life. Evolution cannot build ATP, because evolutionary processes require ATP to even function - creating a massive chicken-or-the-egg paradox. You can't have life without ATP, but you can't get ATP until you have life. Evidence it was intelligently designed. ATP Synthase is also incredibly complex. In simpler prokaryotic organisms (bacteria, etc), the molecule has 8 unique proteins organized into 22 subunits, all working together in a coordinated system. In higher level eukaryotes (humans, mammals, etc), the molecule has 18 unique proteins organized into 29 coordinated subunits making up the system. The simpler versions still require a minimal set of specified proteins, totaling more than 3,500 amino acids, sequenced perfectly in line to create all the proteins, all engineered to perfection. The odds of something like this coming together by chance are incomprehensibly small, it's effectively impossible. This system is a clear and obvious sign of design.
0:57

This is how cells make energy - the production of ATP. All life requires ATP for energy. Without it, cells cannot function, and Life cannot survive. That means ATP Synthase is required from the very start of Life. Evolution cannot build ATP, because evolutionary processes require ATP to even function - creating a massive chicken-or-the-egg paradox. You can't have life without ATP, but you can't get ATP until you have life. Evidence it was intelligently designed. ATP Synthase is also incredibly complex. In simpler prokaryotic organisms (bacteria, etc), the molecule has 8 unique proteins organized into 22 subunits, all working together in a coordinated system. In higher level eukaryotes (humans, mammals, etc), the molecule has 18 unique proteins organized into 29 coordinated subunits making up the system. The simpler versions still require a minimal set of specified proteins, totaling more than 3,500 amino acids, sequenced perfectly in line to create all the proteins, all engineered to perfection. The odds of something like this coming together by chance are incomprehensibly small, it's effectively impossible. This system is a clear and obvious sign of design.

Divinely Designed

61,199 Aufrufe • vor 6 Monaten

🔥 SURGEON WARNS THE BIGGEST BREAKTHROUGH IN HUMAN HISTORY IS HAPPENING RIGHT NOW — “BIGGER THAN AI” A surgeon is going viral after claiming scientists may have already discovered a way to partially REVERSE aging at the DNA level… and he says the implications are bigger than AI, social media, smartphones, or even the internet itself. Dr. Buck Parker’s claim: “The fountain of youth has been discovered.” “This is bigger than the Industrial Revolution. Bigger than the advent of the internet. Bigger than Amazon, Apple, the iPhone, Google, social media… bigger than AI.” And according to Dr. Parker… it’s already happening RIGHT NOW. The core claim revolves around something called “Yamanaka factors,” proteins discovered by Nobel Prize-winning researcher Shinya Yamanaka that can reportedly reset damaged cells back to a younger biological state. According to Dr. Parker: •Scientists have reportedly reversed visible signs of aging in animals •Wrinkled skin in test subjects appeared to become youthful again •Researchers are now experimenting with literally “turning back” cellular age •Human trials are reportedly beginning •Some scientists now believe aging itself may simply be accumulated DNA damage His warning: “If you’ve been alive for the last 40 years… you’ve seen some wild sh*t happen. It’s about to get more wild.” If this became available tomorrow… would you actually take it? I’m lining up ‼️‼️‼️😂😂😂 Note that while Yamanaka factors are real (Shinya Yamanaka won the Nobel Prize in 2012 for induced pluripotent stem cells), the dramatic claims about immediate “fountain of youth” breakthroughs and human trials should be approached with caution and verified through scientific sources.
5:22

🔥 SURGEON WARNS THE BIGGEST BREAKTHROUGH IN HUMAN HISTORY IS HAPPENING RIGHT NOW — “BIGGER THAN AI” A surgeon is going viral after claiming scientists may have already discovered a way to partially REVERSE aging at the DNA level… and he says the implications are bigger than AI, social media, smartphones, or even the internet itself. Dr. Buck Parker’s claim: “The fountain of youth has been discovered.” “This is bigger than the Industrial Revolution. Bigger than the advent of the internet. Bigger than Amazon, Apple, the iPhone, Google, social media… bigger than AI.” And according to Dr. Parker… it’s already happening RIGHT NOW. The core claim revolves around something called “Yamanaka factors,” proteins discovered by Nobel Prize-winning researcher Shinya Yamanaka that can reportedly reset damaged cells back to a younger biological state. According to Dr. Parker: •Scientists have reportedly reversed visible signs of aging in animals •Wrinkled skin in test subjects appeared to become youthful again •Researchers are now experimenting with literally “turning back” cellular age •Human trials are reportedly beginning •Some scientists now believe aging itself may simply be accumulated DNA damage His warning: “If you’ve been alive for the last 40 years… you’ve seen some wild sh*t happen. It’s about to get more wild.” If this became available tomorrow… would you actually take it? I’m lining up ‼️‼️‼️😂😂😂 Note that while Yamanaka factors are real (Shinya Yamanaka won the Nobel Prize in 2012 for induced pluripotent stem cells), the dramatic claims about immediate “fountain of youth” breakthroughs and human trials should be approached with caution and verified through scientific sources.

MR. Q-17

257,904 Aufrufe • vor 4 Tagen

🔥 SURGEON WARNS THE BIGGEST BREAKTHROUGH IN HUMAN HISTORY IS HAPPENING RIGHT NOW — “BIGGER THAN AI” A surgeon is going viral after claiming scientists may have already discovered a way to partially REVERSE aging at the DNA level… and he says the implications are bigger than AI, social media, smartphones, or even the internet itself. Dr. Buck Parker’s claim: “The fountain of youth has been discovered.” “This is bigger than the Industrial Revolution. Bigger than the advent of the internet. Bigger than Amazon, Apple, the iPhone, Google, social media… bigger than AI.” And according to Dr. Parker… it’s already happening RIGHT NOW. The core claim revolves around something called “Yamanaka factors,” proteins discovered by Nobel Prize-winning researcher Shinya Yamanaka that can reportedly reset damaged cells back to a younger biological state. According to Dr. Parker: •Scientists have reportedly reversed visible signs of aging in animals •Wrinkled skin in test subjects appeared to become youthful again •Researchers are now experimenting with literally “turning back” cellular age •Human trials are reportedly beginning •Some scientists now believe aging itself may simply be accumulated DNA damage His warning: “If you’ve been alive for the last 40 years… you’ve seen some wild sh*t happen. It’s about to get more wild.” If this became available tomorrow… would you actually take it? I’m lining up ‼️‼️‼️😂😂😂 Note that while Yamanaka factors are real (Shinya Yamanaka won the Nobel Prize in 2012 for induced pluripotent stem cells), the dramatic claims about immediate “fountain of youth” breakthroughs and human trials should be approached with caution and verified through scientific sources.
5:22

🔥 SURGEON WARNS THE BIGGEST BREAKTHROUGH IN HUMAN HISTORY IS HAPPENING RIGHT NOW — “BIGGER THAN AI” A surgeon is going viral after claiming scientists may have already discovered a way to partially REVERSE aging at the DNA level… and he says the implications are bigger than AI, social media, smartphones, or even the internet itself. Dr. Buck Parker’s claim: “The fountain of youth has been discovered.” “This is bigger than the Industrial Revolution. Bigger than the advent of the internet. Bigger than Amazon, Apple, the iPhone, Google, social media… bigger than AI.” And according to Dr. Parker… it’s already happening RIGHT NOW. The core claim revolves around something called “Yamanaka factors,” proteins discovered by Nobel Prize-winning researcher Shinya Yamanaka that can reportedly reset damaged cells back to a younger biological state. According to Dr. Parker: •Scientists have reportedly reversed visible signs of aging in animals •Wrinkled skin in test subjects appeared to become youthful again •Researchers are now experimenting with literally “turning back” cellular age •Human trials are reportedly beginning •Some scientists now believe aging itself may simply be accumulated DNA damage His warning: “If you’ve been alive for the last 40 years… you’ve seen some wild sh*t happen. It’s about to get more wild.” If this became available tomorrow… would you actually take it? I’m lining up ‼️‼️‼️😂😂😂 Note that while Yamanaka factors are real (Shinya Yamanaka won the Nobel Prize in 2012 for induced pluripotent stem cells), the dramatic claims about immediate “fountain of youth” breakthroughs and human trials should be approached with caution and verified through scientific sources.

GP Q

284,013 Aufrufe • vor 2 Monaten

A molecular biologist's devastating critique of mRNA COVID-19 vaccines, outlining why they must be stopped. According to Dr. Janci Chunn Lindsey, a PhD molecular biologist and toxicologist, the public has been misled about the fundamental nature of COVID-19 mRNA vaccines. She identifies them not as traditional vaccines, but as gene therapies—a claim she states was falsely denied from the outset. The core mechanism is this: your cells are instructed to produce a foreign viral protein (the spike protein), which your body is then triggered to attack. The critical issue? The genetic material doesn't stay in the arm as promised. It travels systemically, reaching the brain, bone marrow, ovaries, and testes. This widespread distribution means your own cells, in vital organs, become targets for your immune system. Dr. Lindsey links this to an explosion in autoimmunity and severe reproductive issues, citing a concerning similarity between the spike protein and syncytin proteins, which are essential for placental formation and fertility. Perhaps most alarmingly, she raises a specter from 30 years of gene therapy research: the risk of creating transgenic humans. With the genetic material confirmed in ovaries and testes, no studies have investigated if sperm or ova are transfected, potentially passing this genetic code to partners or children. She states plummeting birth rates and increased miscarriages are consistent with this risk. The initial assurances of mRNA's brief stability are also labeled a lie. Modifications make the RNA both highly stable and toxic to mitochondria. Studies have found mRNA in lymph nodes after 60 days and spike protein in the brain after 9 months. Furthermore, claims that the material would not interfere with DNA are challenged. Dr. Lindsey cites studies showing the genetic material does enter the nucleus, impairs DNA repair proteins, and can be reverse-transcribed into the human genome, posing a mutagenic risk that aligns with the observed increase in cancers. In conclusion, she states that past vaccines were pulled for far fewer casualties. Now, with children suffering heart attacks and strokes, regulatory bodies are absent. Her urgent call: to protect our children and our future, these shots must be stopped.
5:08

A molecular biologist's devastating critique of mRNA COVID-19 vaccines, outlining why they must be stopped. According to Dr. Janci Chunn Lindsey, a PhD molecular biologist and toxicologist, the public has been misled about the fundamental nature of COVID-19 mRNA vaccines. She identifies them not as traditional vaccines, but as gene therapies—a claim she states was falsely denied from the outset. The core mechanism is this: your cells are instructed to produce a foreign viral protein (the spike protein), which your body is then triggered to attack. The critical issue? The genetic material doesn't stay in the arm as promised. It travels systemically, reaching the brain, bone marrow, ovaries, and testes. This widespread distribution means your own cells, in vital organs, become targets for your immune system. Dr. Lindsey links this to an explosion in autoimmunity and severe reproductive issues, citing a concerning similarity between the spike protein and syncytin proteins, which are essential for placental formation and fertility. Perhaps most alarmingly, she raises a specter from 30 years of gene therapy research: the risk of creating transgenic humans. With the genetic material confirmed in ovaries and testes, no studies have investigated if sperm or ova are transfected, potentially passing this genetic code to partners or children. She states plummeting birth rates and increased miscarriages are consistent with this risk. The initial assurances of mRNA's brief stability are also labeled a lie. Modifications make the RNA both highly stable and toxic to mitochondria. Studies have found mRNA in lymph nodes after 60 days and spike protein in the brain after 9 months. Furthermore, claims that the material would not interfere with DNA are challenged. Dr. Lindsey cites studies showing the genetic material does enter the nucleus, impairs DNA repair proteins, and can be reverse-transcribed into the human genome, posing a mutagenic risk that aligns with the observed increase in cancers. In conclusion, she states that past vaccines were pulled for far fewer casualties. Now, with children suffering heart attacks and strokes, regulatory bodies are absent. Her urgent call: to protect our children and our future, these shots must be stopped.

Camus

178,794 Aufrufe • vor 10 Monaten

🚨🚨🚨🚨 Oh-oh! First experiments of genetic vaccines getting absorbed by human cells completed - Prof Sucharit Bhakdi reveals. ----------------------------- Our two lady scientists who are just brilliant, they took cells, human cells, and immersed these cells in the vaccine and they found, and these are the first experiments that have ever been done, okay, that the human cells immediately took up the vaccines and the DNA and the chromosomes, and the chromosomes, bacterial chromosomes, entered the cells and these cells immediately started making the spike protein in horrendous quantity and they have quantified this, they have shown what happens to the spike protein, that it is stable, that it is shed into the blood, into the circulation, they have shown that they can measure this in the blood, they can measure this anywhere actually, and they have shown that the plasmid and the spike production goes on for many, many days. So, what did our girls do? They sent their human cells that had been transfected to Kevin McKernan, begging the question, Kevin, can you find any chromosomal integration of bacterial DNA in the human cell chromosomes? Do you know the answer? He put it up in his substack one week ago, and the answer is yes. He's found it. ------------------------------------- Kevin McKernan
5:27

🚨🚨🚨🚨 Oh-oh! First experiments of genetic vaccines getting absorbed by human cells completed - Prof Sucharit Bhakdi reveals. ----------------------------- Our two lady scientists who are just brilliant, they took cells, human cells, and immersed these cells in the vaccine and they found, and these are the first experiments that have ever been done, okay, that the human cells immediately took up the vaccines and the DNA and the chromosomes, and the chromosomes, bacterial chromosomes, entered the cells and these cells immediately started making the spike protein in horrendous quantity and they have quantified this, they have shown what happens to the spike protein, that it is stable, that it is shed into the blood, into the circulation, they have shown that they can measure this in the blood, they can measure this anywhere actually, and they have shown that the plasmid and the spike production goes on for many, many days. So, what did our girls do? They sent their human cells that had been transfected to Kevin McKernan, begging the question, Kevin, can you find any chromosomal integration of bacterial DNA in the human cell chromosomes? Do you know the answer? He put it up in his substack one week ago, and the answer is yes. He's found it. ------------------------------------- Kevin McKernan

aussie17

333,911 Aufrufe • vor 2 Jahren