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🚨mRNA "Vaccination" Causes INSTANT Biological Damage A new study found that within 48 hours of an mRNA booster, healthy young adults suffered: 🩸D‑dimer spikes → dangerous clotting 📉Lymphocytes crash → immune collapse 🔥CRP surges → systemic inflammation

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Nicolas Hulscher, MPH

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62,095 görüntüleme • 7 ay önce •via X (Twitter)

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🚨THOUSANDS of Genes Disrupted by mRNA Shots Our new study discovered that mRNA technology induces long-term genetic damage and biochemical HAVOC — turning genes on/off in ways that fuel cancer, clotting, hyper-inflammation, mitochondrial failure and immune collapse.
0:55

🚨THOUSANDS of Genes Disrupted by mRNA Shots Our new study discovered that mRNA technology induces long-term genetic damage and biochemical HAVOC — turning genes on/off in ways that fuel cancer, clotting, hyper-inflammation, mitochondrial failure and immune collapse.

Nicolas Hulscher, MPH

40,939 görüntüleme • 7 ay önce

🚨mRNA SHOTS REPROGRAM THOUSANDS OF CRITICAL GENES Our study discovered that COVID-19 mRNA injections induce long-term genetic damage and biochemical HAVOC — turning genes on/off in ways that fuel cancer, clotting, hyper-inflammation, mitochondrial failure and immune collapse.
1:01

🚨mRNA SHOTS REPROGRAM THOUSANDS OF CRITICAL GENES Our study discovered that COVID-19 mRNA injections induce long-term genetic damage and biochemical HAVOC — turning genes on/off in ways that fuel cancer, clotting, hyper-inflammation, mitochondrial failure and immune collapse.

Nicolas Hulscher, MPH

40,660 görüntüleme • 4 ay önce

"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 görüntüleme • 1 yıl önce

DISTURBING: It’s no longer a theory. A new study has confirmed devastating genetic damage caused by the COVID-19 mRNA vaccines, including the activation of cancer-causing genes and breakdowns in the immune system. The study, titled “Synthetic mRNA Vaccines and Transcriptomic Dysregulation,” reveals how these mRNA injections disrupt thousands of vital genes. Using advanced RNA sequencing, scientists uncovered mitochondrial failure, immune system reprogramming, and oncogenic activation—damage that could persist for years and wreak havoc across generations. But here’s the most alarming part: these vaccines don’t just harm the vaccinated—they pose a threat to the entire global population. With millions already injected, the study warns that these genetic alterations could lead to cancers and chronic diseases, impacting generations to come. And it gets worse: the vaccines can shed onto the unvaccinated, spreading their toxic effects even further. In addition, the mRNA boosters are causing dangerous blood clotting and immune suppression in healthy young adults within just 48 hours. And as if that wasn’t enough, pets receiving mRNA vaccines could be shedding toxic particles directly onto their owners, escalating the risk exponentially. This is no longer a debate—it’s a full-blown global health emergency unfolding before our eyes. The smoking gun is right here, and the evidence is undeniable. How much longer can we afford to ignore these findings? Watch 's shocking report with Nicolas Hulscher, MPH to learn what this means for our future.
15:24

DISTURBING: It’s no longer a theory. A new study has confirmed devastating genetic damage caused by the COVID-19 mRNA vaccines, including the activation of cancer-causing genes and breakdowns in the immune system. The study, titled “Synthetic mRNA Vaccines and Transcriptomic Dysregulation,” reveals how these mRNA injections disrupt thousands of vital genes. Using advanced RNA sequencing, scientists uncovered mitochondrial failure, immune system reprogramming, and oncogenic activation—damage that could persist for years and wreak havoc across generations. But here’s the most alarming part: these vaccines don’t just harm the vaccinated—they pose a threat to the entire global population. With millions already injected, the study warns that these genetic alterations could lead to cancers and chronic diseases, impacting generations to come. And it gets worse: the vaccines can shed onto the unvaccinated, spreading their toxic effects even further. In addition, the mRNA boosters are causing dangerous blood clotting and immune suppression in healthy young adults within just 48 hours. And as if that wasn’t enough, pets receiving mRNA vaccines could be shedding toxic particles directly onto their owners, escalating the risk exponentially. This is no longer a debate—it’s a full-blown global health emergency unfolding before our eyes. The smoking gun is right here, and the evidence is undeniable. How much longer can we afford to ignore these findings? Watch 's shocking report with Nicolas Hulscher, MPH to learn what this means for our future.

The Vigilant Fox 🦊

266,820 görüntüleme • 1 yıl önce

🚨THREE INDEPENDENT SOURCES CONFIRM: Pfizer/Moderna mRNA Shots Alter the Human Genome 📌 Aldén et al: Pfizer mRNA reverse-transcribed into DNA in liver cells—within 6 hours 📌 InModia Lab (Germany): Spike + SV40 found in human tissue years later 📌 Neo7Bioscience + Univ. of North Texas: Persistent synthetic RNA, SV40, and cancer-linked gene dysregulation in vaccinated blood Some may become permanent spike factories—driving chronic inflammation, immune collapse, and cancer. As regulators remain silent, we will continue to study these deeply worrisome findings.
0:57

🚨THREE INDEPENDENT SOURCES CONFIRM: Pfizer/Moderna mRNA Shots Alter the Human Genome 📌 Aldén et al: Pfizer mRNA reverse-transcribed into DNA in liver cells—within 6 hours 📌 InModia Lab (Germany): Spike + SV40 found in human tissue years later 📌 Neo7Bioscience + Univ. of North Texas: Persistent synthetic RNA, SV40, and cancer-linked gene dysregulation in vaccinated blood Some may become permanent spike factories—driving chronic inflammation, immune collapse, and cancer. As regulators remain silent, we will continue to study these deeply worrisome findings.

Nicolas Hulscher, MPH

138,008 görüntüleme • 1 yıl önce

REPORT: A new study confirms that COVID-19 mRNA injections spread to vital organs and trigger systemic, toxic spike protein production. This “conspiracy theory” just became a reality. The new study, published in Nature Biotechnology, reveals alarming details about the biodistribution of lipid nanoparticles (LNPs) carrying SARS-CoV-2 spike mRNA. The study demonstrated that even at extremely low doses (0.0005 mg/kg), these LNPs deliver mRNA to cells in vital organs, leading to the production of toxic spike protein. According to the researchers, this protein triggers immune activation and causes damage to blood vessels. Meanwhile, autopsy findings now confirm the systemic presence of spike protein in tissues and organs, raising serious questions about the safety of these so-called vaccines. Epidemiologist Nicolas Hulscher, MPH didn’t hold back in his response to the news of this study, stating: “Biodistribution studies should have been performed BEFORE mass ‘vaccination’ of the entire world’s population. These invasive gene therapy injections must be pulled from global markets immediately.”
3:39

REPORT: A new study confirms that COVID-19 mRNA injections spread to vital organs and trigger systemic, toxic spike protein production. This “conspiracy theory” just became a reality. The new study, published in Nature Biotechnology, reveals alarming details about the biodistribution of lipid nanoparticles (LNPs) carrying SARS-CoV-2 spike mRNA. The study demonstrated that even at extremely low doses (0.0005 mg/kg), these LNPs deliver mRNA to cells in vital organs, leading to the production of toxic spike protein. According to the researchers, this protein triggers immune activation and causes damage to blood vessels. Meanwhile, autopsy findings now confirm the systemic presence of spike protein in tissues and organs, raising serious questions about the safety of these so-called vaccines. Epidemiologist Nicolas Hulscher, MPH didn’t hold back in his response to the news of this study, stating: “Biodistribution studies should have been performed BEFORE mass ‘vaccination’ of the entire world’s population. These invasive gene therapy injections must be pulled from global markets immediately.”

The Vigilant Fox 🦊

396,969 görüntüleme • 1 yıl önce

'mRNA COVID Vaccines Caused 74% Of Sudden Deaths Within 7 Days Of Vaccination & Many Within The 1st 72 Hours.' It Is The Largest Autopsy Series In The World. People Who Dropped Dead After The COVID-19 Vaccine, It Was Determined That 73.9% Of Individuals Died FROM The Vaccines. Causality in each case was determined by three independent reviewers with cardiac pathology experience & expertise. The number of days from last COVID-19 vaccination until death was 6.2 & 3 days, respectively. Most of the deaths occurred within a week from the last injection. The deaths were causally linked to COVID-19 vaccination by independent adjudication. The predominant COVID-19 vaccine platforms include messenger RNA (mRNA) Pfizer, Moderna, AstraZeneca, Johnson & Johnson, Novavax & Zifi Vax – mRNA & viral vector vaccines involve the bodily synthesis of the SARS-CoV-2 Spike protein as the foundation of the immune response. Regardless of the vaccine platform used, circulating SARS-CoV-2 Spike protein is the detrimental agent through which COVID-19 vaccines cause biological harm. Here Is The 'How & Why' Of The Spike Protein Mechanism That Leads To Harm & Death: Spike protein initiates the breakdown & internalization of ACE2 receptors, which disrupts the renin–angiotensin system (RAS) & lead to increased inflammation, vasoconstriction & thrombosis. Further, Spike 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 & Spike protein, resulting in drastic inflammation. Long term immune surveillance is compromised by mRNA COVID-19 vaccines due to IRF7, IRF9, p53 & BRCA suppression. There is a causal link between COVID-19 mRNA vaccination & myocarditis, neurodegenerative disease, immune thrombocytopenia, Bell's palsy, liver disease, impaired adaptive immunity, impeded DNA damage response and tumorigenesis. Moreover, a recent study found that repeated COVID-19 vaccination with mRNA-based vaccines leads to the production of abnormally high concentrations of IgG4 antibodies. These antibodies fail to neutralize Spike protein, which has been shown to circulate for at least 28 days, cause immune suppression & promote the development of autoimmune diseases including myocarditis. 👇Fatal COVID-19 Vaccine-Induced Myocarditis👇 👇Cardiac Arrest After COVID-19 Vaccination👇 Speaker: Dr William Makis Video: @the_barefoot_truther
1:18

'mRNA COVID Vaccines Caused 74% Of Sudden Deaths Within 7 Days Of Vaccination & Many Within The 1st 72 Hours.' It Is The Largest Autopsy Series In The World. People Who Dropped Dead After The COVID-19 Vaccine, It Was Determined That 73.9% Of Individuals Died FROM The Vaccines. Causality in each case was determined by three independent reviewers with cardiac pathology experience & expertise. The number of days from last COVID-19 vaccination until death was 6.2 & 3 days, respectively. Most of the deaths occurred within a week from the last injection. The deaths were causally linked to COVID-19 vaccination by independent adjudication. The predominant COVID-19 vaccine platforms include messenger RNA (mRNA) Pfizer, Moderna, AstraZeneca, Johnson & Johnson, Novavax & Zifi Vax – mRNA & viral vector vaccines involve the bodily synthesis of the SARS-CoV-2 Spike protein as the foundation of the immune response. Regardless of the vaccine platform used, circulating SARS-CoV-2 Spike protein is the detrimental agent through which COVID-19 vaccines cause biological harm. Here Is The 'How & Why' Of The Spike Protein Mechanism That Leads To Harm & Death: Spike protein initiates the breakdown & internalization of ACE2 receptors, which disrupts the renin–angiotensin system (RAS) & lead to increased inflammation, vasoconstriction & thrombosis. Further, Spike 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 & Spike protein, resulting in drastic inflammation. Long term immune surveillance is compromised by mRNA COVID-19 vaccines due to IRF7, IRF9, p53 & BRCA suppression. There is a causal link between COVID-19 mRNA vaccination & myocarditis, neurodegenerative disease, immune thrombocytopenia, Bell's palsy, liver disease, impaired adaptive immunity, impeded DNA damage response and tumorigenesis. Moreover, a recent study found that repeated COVID-19 vaccination with mRNA-based vaccines leads to the production of abnormally high concentrations of IgG4 antibodies. These antibodies fail to neutralize Spike protein, which has been shown to circulate for at least 28 days, cause immune suppression & promote the development of autoimmune diseases including myocarditis. 👇Fatal COVID-19 Vaccine-Induced Myocarditis👇 👇Cardiac Arrest After COVID-19 Vaccination👇 Speaker: Dr William Makis Video: @the_barefoot_truther

Valerie Anne Smith

17,753 görüntüleme • 1 yıl önce

This is very concerning… 🚨 Japan Scientists just released an Earth-Shattering Report after analyzing 21 Million COVID Vaccination Records • A group of thousands of Japanese scientists, researchers, and volunteers, led by the United Citizens for Stopping mRNA Vaccines, has unleashed a massive 21 million vaccination records report • By analyzing the 21 million records, Prof Murakami of Tokyo Science University uncovered a disturbing peak in deaths 90–120 days after mRNA vaccination, with extremely higher death rates in vaccinated individuals • Murakami estimates that approximately 600,000 Japanese may have died post-vaccination, a figure that aligns eerily with Japan’s excess death statistics. - Younger age groups, particularly those aged 20–29, exhibited higher excess death rates post-vaccination compared to older groups • Data indicates that COVID mRNA vaccines deactivates and turns your immune system into a weapon against you. • Data shows additional booster doses correlated with increased infection rates and higher mortality, with vaccinated individuals showing greater susceptibility to infections. - The study highlighted a significant rise in cancer-related deaths and cardiovascular issues, including heart failure, among vaccinated individuals It’s time to pull every single mRNA vaccines off the market.
10:15

This is very concerning… 🚨 Japan Scientists just released an Earth-Shattering Report after analyzing 21 Million COVID Vaccination Records • A group of thousands of Japanese scientists, researchers, and volunteers, led by the United Citizens for Stopping mRNA Vaccines, has unleashed a massive 21 million vaccination records report • By analyzing the 21 million records, Prof Murakami of Tokyo Science University uncovered a disturbing peak in deaths 90–120 days after mRNA vaccination, with extremely higher death rates in vaccinated individuals • Murakami estimates that approximately 600,000 Japanese may have died post-vaccination, a figure that aligns eerily with Japan’s excess death statistics. - Younger age groups, particularly those aged 20–29, exhibited higher excess death rates post-vaccination compared to older groups • Data indicates that COVID mRNA vaccines deactivates and turns your immune system into a weapon against you. • Data shows additional booster doses correlated with increased infection rates and higher mortality, with vaccinated individuals showing greater susceptibility to infections. - The study highlighted a significant rise in cancer-related deaths and cardiovascular issues, including heart failure, among vaccinated individuals It’s time to pull every single mRNA vaccines off the market.

MJTruthUltra

150,873 görüntüleme • 1 yıl önce

"It Was Clear From The Beginning, The Illness Of COVID Was Actually All About The Vaccine...A Needle Into Every Arm." Dr Peter McCullough, MD The Vaccine Did Not Save Millions Of Lives...The Shots Contain A Killer Protein That Cannot Be Turned Off...It Was Not Safe By Design. The predominant COVID-19 vaccine platforms include messenger RNA (mRNA) Pfizer, Moderna, AstraZeneca, Johnson & Johnson, Novavax & Zifi Vax – mRNA & viral vector vaccines involve the bodily synthesis of the SARS-CoV-2 Spike protein as the foundation of the immune response. Regardless of the vaccine platform used, circulating SARS-CoV-2 Spike protein is the detrimental agent through which COVID-19 vaccines cause biological harm. Here Is The 'How & Why' Of The Spike Protein Mechanism That Leads To Harm & Death: Spike protein initiates the breakdown & internalization of ACE2 receptors, which disrupts the renin–angiotensin system (RAS) & lead to increased inflammation, vasoconstriction & thrombosis. Further, Spike 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 & Spike protein, resulting in drastic inflammation. Long term immune surveillance is compromised by mRNA COVID-19 vaccines due to IRF7, IRF9, p53 & BRCA suppression. There is a causal link between COVID-19 mRNA vaccination & myocarditis, neurodegenerative disease, immune thrombocytopenia, Bell's palsy, liver disease, impaired adaptive immunity, impeded DNA damage response and tumorigenesis. Moreover, a recent study found that repeated COVID-19 vaccination with mRNA-based vaccines leads to the production of abnormally high concentrations of IgG4 antibodies. These antibodies fail to neutralize Spike protein, which has been shown to circulate for at least 28 days, cause immune suppression & promote the development of autoimmune diseases including myocarditis. 👇Fatal COVID-19 Vaccine-Induced Myocarditis👇 👇Cardiac Arrest After COVID-19 Vaccination👇 👇DNA Fragments In Pfizer & Moderna Vaccines👇 Speaker: Peter A. McCullough, MD, MPH® McCullough Foundation
1:28

"It Was Clear From The Beginning, The Illness Of COVID Was Actually All About The Vaccine...A Needle Into Every Arm." Dr Peter McCullough, MD The Vaccine Did Not Save Millions Of Lives...The Shots Contain A Killer Protein That Cannot Be Turned Off...It Was Not Safe By Design. The predominant COVID-19 vaccine platforms include messenger RNA (mRNA) Pfizer, Moderna, AstraZeneca, Johnson & Johnson, Novavax & Zifi Vax – mRNA & viral vector vaccines involve the bodily synthesis of the SARS-CoV-2 Spike protein as the foundation of the immune response. Regardless of the vaccine platform used, circulating SARS-CoV-2 Spike protein is the detrimental agent through which COVID-19 vaccines cause biological harm. Here Is The 'How & Why' Of The Spike Protein Mechanism That Leads To Harm & Death: Spike protein initiates the breakdown & internalization of ACE2 receptors, which disrupts the renin–angiotensin system (RAS) & lead to increased inflammation, vasoconstriction & thrombosis. Further, Spike 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 & Spike protein, resulting in drastic inflammation. Long term immune surveillance is compromised by mRNA COVID-19 vaccines due to IRF7, IRF9, p53 & BRCA suppression. There is a causal link between COVID-19 mRNA vaccination & myocarditis, neurodegenerative disease, immune thrombocytopenia, Bell's palsy, liver disease, impaired adaptive immunity, impeded DNA damage response and tumorigenesis. Moreover, a recent study found that repeated COVID-19 vaccination with mRNA-based vaccines leads to the production of abnormally high concentrations of IgG4 antibodies. These antibodies fail to neutralize Spike protein, which has been shown to circulate for at least 28 days, cause immune suppression & promote the development of autoimmune diseases including myocarditis. 👇Fatal COVID-19 Vaccine-Induced Myocarditis👇 👇Cardiac Arrest After COVID-19 Vaccination👇 👇DNA Fragments In Pfizer & Moderna Vaccines👇 Speaker: Peter A. McCullough, MD, MPH® McCullough Foundation

Valerie Anne Smith

67,928 görüntüleme • 1 yıl önce

Scientists Admit Long COVID Sufferers Are Actually Suffering From V-AIDS...Vaccine Induced AIDS. The World Renowned Yale University Has Confirmed That COVID mRNA Vaccines Cause Vaccine Acquired Immune Deficiency Syndrome. UnVaxxed Long COVID Sufferers Acquire It From Shedding. The Yale University School of Medicine found that mRNA injections alter human biology to create long term S2 spike protein production that increases over time. The scientists warned that the COVID mRNA vaccines alter T-cell immunophenotypes which triggers VAIDS. The study was led by Bornali Bhattacharjee. People not only collectively in essence felt forced to take an experimental vaccine or risk losing their jobs...we were lied to about it. It never stopped transmission, it never stopped contracting it & it was never safe. The mRNA vaccines cause heart issues, blood clots, autoimmune disorders & so many more grave illnesses & death. This is the most egregious scandal in worldwide history. COVID-19 vaccines cause adverse events such as myocarditis & pericarditis, thrombosis & thrombocytopenia, Guillain–Barre syndrome, transverse myelitis & Bell’s Palsy. In addition, individuals have reported post-vaccination symptoms resembling long COVID beginning shortly after vaccination. This condition, sometimes referred to as post-vaccination syndrome (PVS) or post-acute COVID-19 vaccination syndrome (PACVS), is characterized by symptoms such as exercise intolerance, excessive fatigue, numbness, brain fog, neuropathy, insomnia, palpitations, myalgia, tinnitus, headache, burning sensations & dizziness. Finally, we have scientific confirmation that vaccination against COVID-19 causes a marked decrease in immunity to heterologous pathogens such as viruses, bacteria & fungi.’ A condition known as ‘VAIDS’ vaccine-induced AIDS.” COVID mRNA vaccines cause long-term symptoms by multiple mechanisms: 1⃣ Vaccine 80 components, the mRNA lipid nanoparticles & adenoviral vectors, trigger activation of pattern recognition receptors. Thus, unregulated stimulation of innate immunity leads to chronic inflammation. 2⃣ The S2 spike protein expressed following BNT162b2 or mRNA-1273 vaccination circulates in the plasma as early as one day after vaccination. Interaction with full-length S2 spike, its subunits (S1, S2), and/or peptide fragments with host molecules result in prolonged symptoms. Recently, a subset of non-classical monocytes has been shown to harbor S2 spike protein in patients with PVS18. Further, biodistribution studies on mRNA–LNP platforms in animal models indicate its ability to cross the blood-brain barrier, and the local S2 expression results in neurocognitive symptoms. 3⃣ Vaccine-induced VAIDS immune responses are triggering the stimulation of autoreactive lymphocytes. If you or someone you love is suffering from Long COVID, there are 2 paths to detoxification & healing...& both protocols can also be taken together if desired. 1⃣ Dr Peter McCullough's Detox Protocol involving 3 supplements that detox the spike protein & Inflammation (Link #3 below) 2⃣ Pure Body Zeolite Detoxification Drops that target toxins, chemicals & chelation of heavy metals (Link #4 below) 👇Yale Study: COVID mRNA Cause V-AIDS👇 👇COVID mRNA Vaccines Suppress Immunity👇 👇COVID mRNA Vaccine Detoxification Protoc👇 👇Pure Body Heavy Metal Detox Zeolite Drops👇 Speaker: @officiallizwheeler
1:29

Scientists Admit Long COVID Sufferers Are Actually Suffering From V-AIDS...Vaccine Induced AIDS. The World Renowned Yale University Has Confirmed That COVID mRNA Vaccines Cause Vaccine Acquired Immune Deficiency Syndrome. UnVaxxed Long COVID Sufferers Acquire It From Shedding. The Yale University School of Medicine found that mRNA injections alter human biology to create long term S2 spike protein production that increases over time. The scientists warned that the COVID mRNA vaccines alter T-cell immunophenotypes which triggers VAIDS. The study was led by Bornali Bhattacharjee. People not only collectively in essence felt forced to take an experimental vaccine or risk losing their jobs...we were lied to about it. It never stopped transmission, it never stopped contracting it & it was never safe. The mRNA vaccines cause heart issues, blood clots, autoimmune disorders & so many more grave illnesses & death. This is the most egregious scandal in worldwide history. COVID-19 vaccines cause adverse events such as myocarditis & pericarditis, thrombosis & thrombocytopenia, Guillain–Barre syndrome, transverse myelitis & Bell’s Palsy. In addition, individuals have reported post-vaccination symptoms resembling long COVID beginning shortly after vaccination. This condition, sometimes referred to as post-vaccination syndrome (PVS) or post-acute COVID-19 vaccination syndrome (PACVS), is characterized by symptoms such as exercise intolerance, excessive fatigue, numbness, brain fog, neuropathy, insomnia, palpitations, myalgia, tinnitus, headache, burning sensations & dizziness. Finally, we have scientific confirmation that vaccination against COVID-19 causes a marked decrease in immunity to heterologous pathogens such as viruses, bacteria & fungi.’ A condition known as ‘VAIDS’ vaccine-induced AIDS.” COVID mRNA vaccines cause long-term symptoms by multiple mechanisms: 1⃣ Vaccine 80 components, the mRNA lipid nanoparticles & adenoviral vectors, trigger activation of pattern recognition receptors. Thus, unregulated stimulation of innate immunity leads to chronic inflammation. 2⃣ The S2 spike protein expressed following BNT162b2 or mRNA-1273 vaccination circulates in the plasma as early as one day after vaccination. Interaction with full-length S2 spike, its subunits (S1, S2), and/or peptide fragments with host molecules result in prolonged symptoms. Recently, a subset of non-classical monocytes has been shown to harbor S2 spike protein in patients with PVS18. Further, biodistribution studies on mRNA–LNP platforms in animal models indicate its ability to cross the blood-brain barrier, and the local S2 expression results in neurocognitive symptoms. 3⃣ Vaccine-induced VAIDS immune responses are triggering the stimulation of autoreactive lymphocytes. If you or someone you love is suffering from Long COVID, there are 2 paths to detoxification & healing...& both protocols can also be taken together if desired. 1⃣ Dr Peter McCullough's Detox Protocol involving 3 supplements that detox the spike protein & Inflammation (Link #3 below) 2⃣ Pure Body Zeolite Detoxification Drops that target toxins, chemicals & chelation of heavy metals (Link #4 below) 👇Yale Study: COVID mRNA Cause V-AIDS👇 👇COVID mRNA Vaccines Suppress Immunity👇 👇COVID mRNA Vaccine Detoxification Protoc👇 👇Pure Body Heavy Metal Detox Zeolite Drops👇 Speaker: @officiallizwheeler

Valerie Anne Smith

342,842 görüntüleme • 1 yıl önce

Bret Weinstein breaks down the three foundational vaccine technologies, arguing that none are fundamentally safe. Each carries a severe, inherent downside. 1. Live Attenuated Vaccines: The risk here is unpredictability and evolution. A virus weakened for one person may cause a serious infection in another. Crucially, it can revert to a pathogenic, transmissible form—a "contagious vaccine." The historical case of the oral polio vaccine causing numerous polio cases stands as a stark warning. 2. Inactivated Virus/Fragments (with Adjuvant): The problem is immune misdirection. A dead virus alone is unconvincing, requiring an "adjuvant"—a chemical alarm bell. This non-specific signal causes the immune system to "freak out," not just at the target antigen but at anything present, like pollen or gut bacteria. Indiscriminately triggering a systemic immune response is a dangerous gamble. 3. mRNA Technology: The danger is haphazard biodistribution. The mRNA instructions travel unpredictably, instructing cells anywhere in the body to produce the foreign antigen. The immune system then rightly identifies these cells as infected and attacks them. This random destruction of healthy tissue—for instance, in the heart—is an unacceptable and fundamentally unsafe mechanism. The conclusion is sobering: our current technological paradigms for vaccination are built on foundations with profound and unaddressed safety trade-offs.
2:08

Bret Weinstein breaks down the three foundational vaccine technologies, arguing that none are fundamentally safe. Each carries a severe, inherent downside. 1. Live Attenuated Vaccines: The risk here is unpredictability and evolution. A virus weakened for one person may cause a serious infection in another. Crucially, it can revert to a pathogenic, transmissible form—a "contagious vaccine." The historical case of the oral polio vaccine causing numerous polio cases stands as a stark warning. 2. Inactivated Virus/Fragments (with Adjuvant): The problem is immune misdirection. A dead virus alone is unconvincing, requiring an "adjuvant"—a chemical alarm bell. This non-specific signal causes the immune system to "freak out," not just at the target antigen but at anything present, like pollen or gut bacteria. Indiscriminately triggering a systemic immune response is a dangerous gamble. 3. mRNA Technology: The danger is haphazard biodistribution. The mRNA instructions travel unpredictably, instructing cells anywhere in the body to produce the foreign antigen. The immune system then rightly identifies these cells as infected and attacks them. This random destruction of healthy tissue—for instance, in the heart—is an unacceptable and fundamentally unsafe mechanism. The conclusion is sobering: our current technological paradigms for vaccination are built on foundations with profound and unaddressed safety trade-offs.

Camus

216,733 görüntüleme • 10 ay önce

Dr. Jordan Vaughn, a clinician overseeing 170,000 patients annually, testified before the Senate, revealing critical insights on the spike protein’s dangers. As a doctor and researcher, he has witnessed the devastating impact of COVID and mRNA vaccines on millions. The spike protein (S1 subunit) is far from benign. It triggers inflammation, disrupts blood vessels, promotes clotting, and forms amyloid aggregates, impairing oxygen delivery and damaging organs. Patients experience heart racing, brain fog, shortness of breath, and severe fatigue. In his Alabama clinic, Dr. Vaughn uses immunofluorescent microscopy to detect these aggregates in patients—teenagers unable to stand and adults suffering strokes without clear causes. Long COVID and vaccine injuries affect 10-15M Americans. Dr. Vaughn’s clinic has treated ~4,000 such patients, many young and previously healthy. Their struggles are real, life-altering, and often ignored by the system. The mRNA vaccines, promoted as a solution, use lipid nanoparticles (LNPs) to deliver modified mRNA, instructing cells to produce spike protein. Unlike traditional vaccines, this causes uncontrolled spike protein production for unknown durations, spreading to the heart, brain, vasculature, ovaries, and testes. The EMA’s assessment of Pfizer’s vaccine confirmed biodistribution beyond the injection site, contradicting claims it “stays in the arm.” In 2021, Dr. Vaughn treated a 69-year-old patient with unexplained shortness of breath after a second Pfizer dose. Tests ruled out typical causes, but anti-clotting therapy brought rapid relief. This case led him to study how spike protein induces fibrin resistant to breakdown, activates platelets, and damages blood vessels—explaining this case and thousands more. Myocarditis signals emerged in spring 2021, particularly in young males post-mRNA vaccination. The DoD confirmed cases, studies detected spike protein in myocarditis patients, and autopsies linked fatal cases to vaccines. Yet, federal mandates intensified, sidelining these concerns. The CDC and FDA’s inaction—and vaccine promotion—eroded public trust. Patients, coerced by 2021 mandates despite prior infections or health risks, now face disability and dismissal. Informed consent, the cornerstone of medicine, was undermined when regulators withheld critical data.
5:09

Dr. Jordan Vaughn, a clinician overseeing 170,000 patients annually, testified before the Senate, revealing critical insights on the spike protein’s dangers. As a doctor and researcher, he has witnessed the devastating impact of COVID and mRNA vaccines on millions. The spike protein (S1 subunit) is far from benign. It triggers inflammation, disrupts blood vessels, promotes clotting, and forms amyloid aggregates, impairing oxygen delivery and damaging organs. Patients experience heart racing, brain fog, shortness of breath, and severe fatigue. In his Alabama clinic, Dr. Vaughn uses immunofluorescent microscopy to detect these aggregates in patients—teenagers unable to stand and adults suffering strokes without clear causes. Long COVID and vaccine injuries affect 10-15M Americans. Dr. Vaughn’s clinic has treated ~4,000 such patients, many young and previously healthy. Their struggles are real, life-altering, and often ignored by the system. The mRNA vaccines, promoted as a solution, use lipid nanoparticles (LNPs) to deliver modified mRNA, instructing cells to produce spike protein. Unlike traditional vaccines, this causes uncontrolled spike protein production for unknown durations, spreading to the heart, brain, vasculature, ovaries, and testes. The EMA’s assessment of Pfizer’s vaccine confirmed biodistribution beyond the injection site, contradicting claims it “stays in the arm.” In 2021, Dr. Vaughn treated a 69-year-old patient with unexplained shortness of breath after a second Pfizer dose. Tests ruled out typical causes, but anti-clotting therapy brought rapid relief. This case led him to study how spike protein induces fibrin resistant to breakdown, activates platelets, and damages blood vessels—explaining this case and thousands more. Myocarditis signals emerged in spring 2021, particularly in young males post-mRNA vaccination. The DoD confirmed cases, studies detected spike protein in myocarditis patients, and autopsies linked fatal cases to vaccines. Yet, federal mandates intensified, sidelining these concerns. The CDC and FDA’s inaction—and vaccine promotion—eroded public trust. Patients, coerced by 2021 mandates despite prior infections or health risks, now face disability and dismissal. Informed consent, the cornerstone of medicine, was undermined when regulators withheld critical data.

Camus

83,315 görüntüleme • 1 yıl önce

A chilling warning from Brussels: The foundational flaw in mRNA technology that the public was never told. At the launch of Make Europe Healthy Again, researcher Panagis Polykretis delivered a critical message the world needs to hear. While the pharmaceutical industry rushes to expand mRNA use for its speed and profit, a fundamental immunological principle is being overlooked: Any cell that produces a foreign protein is marked for destruction by the immune system. This isn't theoretical. Clear histopathological evidence from biopsies and autopsies confirms the vaccine's genetic material does not stay at the injection site. It enters systemic circulation and spreads uncontrollably throughout the body, including to vital organs like the brain and heart. Once there, the body's own cells are forced to produce the foreign antigen, triggering an immune attack on its own tissues. This is the mechanism behind serious adverse effects, such as myocarditis—a condition Polykretis was the first to hypothesize from the mRNA vaccines. Most alarmingly, this was known. The European Medicines Agency's own assessment report (Pfizer study 185350) from Feb 19, 2021, states on page 47 that biodistribution in rats to most tissues occurred within 48 hours. They knew. Yet, millions across Europe, including pregnant women and infants, were inoculated with these products. This mass experiment was enabled by the silence of the scientific majority. The time for accountability and rigorous, long-term safety studies is now, before this technology is expanded further.
2:26

A chilling warning from Brussels: The foundational flaw in mRNA technology that the public was never told. At the launch of Make Europe Healthy Again, researcher Panagis Polykretis delivered a critical message the world needs to hear. While the pharmaceutical industry rushes to expand mRNA use for its speed and profit, a fundamental immunological principle is being overlooked: Any cell that produces a foreign protein is marked for destruction by the immune system. This isn't theoretical. Clear histopathological evidence from biopsies and autopsies confirms the vaccine's genetic material does not stay at the injection site. It enters systemic circulation and spreads uncontrollably throughout the body, including to vital organs like the brain and heart. Once there, the body's own cells are forced to produce the foreign antigen, triggering an immune attack on its own tissues. This is the mechanism behind serious adverse effects, such as myocarditis—a condition Polykretis was the first to hypothesize from the mRNA vaccines. Most alarmingly, this was known. The European Medicines Agency's own assessment report (Pfizer study 185350) from Feb 19, 2021, states on page 47 that biodistribution in rats to most tissues occurred within 48 hours. They knew. Yet, millions across Europe, including pregnant women and infants, were inoculated with these products. This mass experiment was enabled by the silence of the scientific majority. The time for accountability and rigorous, long-term safety studies is now, before this technology is expanded further.

Camus

103,366 görüntüleme • 9 ay önce

🚨BREAKING: Our CENSORED Study Showing mRNA Injections Induce SEVERE Genetic Disruption Linked to Cancer and Chronic Disease Is Now on PUBMED We declare a MAJOR victory against the Journal Cartel. Using high-resolution RNA sequencing on blood samples, we discovered that COVID-19 “vaccines” SEVERELY disrupt expression of THOUSANDS of genes—triggering mitochondrial failure, immune reprogramming, and cancerous activity that can persist for MONTHS to YEARS post-injection. 🧬Differential gene expression analysis compared mRNA-injured patients (cancer, adverse events) to 803 healthy controls — revealing widespread transcriptomic CHAOS: ⚠️ Mitochondrial failure – Complex I breakdown, oxidative stress, energy collapse ⚠️ Immune reprogramming – Chronic inflammation, ACE2 suppression, TLR hyperactivation ⚠️ Oncogenic activation – MYC up, p53/KRAS down, DNA repair suppression ⚠️ Cellular stress – Ribosome overload, misfolded protein buildup, proteasome activation ⚠️ Epigenetic remodeling – Chromatin shifts, methylation changes, nucleosome displacement ⚠️ Reverse transcription suggested – Patterns consistent with LINE-1 activity and persistent plasmid DNA, raising concern for potential genomic integration or sustained foreign gene expression Earlier this year, our study became one of the most-read and most-downloaded preprints in the world. Shortly thereafter, it was abruptly WIPED from the preprint sever AND ResearchGate. We identified that this unethical removal was likely the result of coordinated Bio-Pharmaceutical Complex pressure and PubPeer Mob attacks, intended to shield the deadly mRNA platform. Their efforts have failed miserably. Now, two things need to happen: 1. Immediate market withdrawal of the mRNA injections 2. Formal RICO investigations into the Academic Journal Cartel and its PubPeer enforcement apparatus
1:25

🚨BREAKING: Our CENSORED Study Showing mRNA Injections Induce SEVERE Genetic Disruption Linked to Cancer and Chronic Disease Is Now on PUBMED We declare a MAJOR victory against the Journal Cartel. Using high-resolution RNA sequencing on blood samples, we discovered that COVID-19 “vaccines” SEVERELY disrupt expression of THOUSANDS of genes—triggering mitochondrial failure, immune reprogramming, and cancerous activity that can persist for MONTHS to YEARS post-injection. 🧬Differential gene expression analysis compared mRNA-injured patients (cancer, adverse events) to 803 healthy controls — revealing widespread transcriptomic CHAOS: ⚠️ Mitochondrial failure – Complex I breakdown, oxidative stress, energy collapse ⚠️ Immune reprogramming – Chronic inflammation, ACE2 suppression, TLR hyperactivation ⚠️ Oncogenic activation – MYC up, p53/KRAS down, DNA repair suppression ⚠️ Cellular stress – Ribosome overload, misfolded protein buildup, proteasome activation ⚠️ Epigenetic remodeling – Chromatin shifts, methylation changes, nucleosome displacement ⚠️ Reverse transcription suggested – Patterns consistent with LINE-1 activity and persistent plasmid DNA, raising concern for potential genomic integration or sustained foreign gene expression Earlier this year, our study became one of the most-read and most-downloaded preprints in the world. Shortly thereafter, it was abruptly WIPED from the preprint sever AND ResearchGate. We identified that this unethical removal was likely the result of coordinated Bio-Pharmaceutical Complex pressure and PubPeer Mob attacks, intended to shield the deadly mRNA platform. Their efforts have failed miserably. Now, two things need to happen: 1. Immediate market withdrawal of the mRNA injections 2. Formal RICO investigations into the Academic Journal Cartel and its PubPeer enforcement apparatus

Nicolas Hulscher, MPH

144,328 görüntüleme • 6 ay önce

Whoa: Autism expert Lyn Redwood, just dropped autopsy evidence in today's ACIP meeting about Thimerosal and Autism "This study, based on autopsy brain tissue from children and adults, found a chronic, ongoing neurological inflammatory process in the brains" Something different is happening. Things are definitely changing 🔥 TRANSCRIPT: The IOM investigation regarding thimerosal-containing vaccines and autism contains several important points. If you read the report, one key finding is that the committee repeatedly noted that large epidemiological studies would not be able to detect a subpopulation that might be more genetically vulnerable, which is one of the hypotheses. The committee also dismissed findings of immune activation and inflammation in the brains of animal models exposed to thimerosal-containing vaccines. This was because they changed the criteria from their 2001 report, which focused on biological plausibility, to biological mechanisms in 2004. At that time, we didn’t fully understand the biological mechanisms. Additionally, the committee stated there was no evidence of neuroinflammation or immune activation in the brains of children with autism. However, one year later, in 2005, a landmark study published by Carlos Pardo documented exactly that. This study, based on autopsy brain tissue from children and adults, found a chronic, ongoing neuroinflammatory process in the brains. Today, those findings have been replicated repeatedly and are considered one of the hallmarks of autism. I also wanted to mention a study published by the CDC, led by Dr. Thompson, titled “Early Thimerosal Exposure and Neuropsychological Outcomes at 7 to 10 Years.” They found an association with tics, which can be very debilitating. So, there have been studies that have found evidence of harm. Those were the two main comments I wanted to make. There was another point I intended to raise, but I can’t recall it right now. However, there is evidence, and I can provide studies to support this."
2:19

Whoa: Autism expert Lyn Redwood, just dropped autopsy evidence in today's ACIP meeting about Thimerosal and Autism "This study, based on autopsy brain tissue from children and adults, found a chronic, ongoing neurological inflammatory process in the brains" Something different is happening. Things are definitely changing 🔥 TRANSCRIPT: The IOM investigation regarding thimerosal-containing vaccines and autism contains several important points. If you read the report, one key finding is that the committee repeatedly noted that large epidemiological studies would not be able to detect a subpopulation that might be more genetically vulnerable, which is one of the hypotheses. The committee also dismissed findings of immune activation and inflammation in the brains of animal models exposed to thimerosal-containing vaccines. This was because they changed the criteria from their 2001 report, which focused on biological plausibility, to biological mechanisms in 2004. At that time, we didn’t fully understand the biological mechanisms. Additionally, the committee stated there was no evidence of neuroinflammation or immune activation in the brains of children with autism. However, one year later, in 2005, a landmark study published by Carlos Pardo documented exactly that. This study, based on autopsy brain tissue from children and adults, found a chronic, ongoing neuroinflammatory process in the brains. Today, those findings have been replicated repeatedly and are considered one of the hallmarks of autism. I also wanted to mention a study published by the CDC, led by Dr. Thompson, titled “Early Thimerosal Exposure and Neuropsychological Outcomes at 7 to 10 Years.” They found an association with tics, which can be very debilitating. So, there have been studies that have found evidence of harm. Those were the two main comments I wanted to make. There was another point I intended to raise, but I can’t recall it right now. However, there is evidence, and I can provide studies to support this."

Humanspective

17,425 görüntüleme • 1 yıl önce

Professor Emeritus Yasufumi Murakami of Tokyo University of Science: "It is almost certain that vaccines are contaminated with DNA. mRNA vaccines containing the DNA causes turbo cancers." Professor Murakami explains the mechanism of turbo cancers: The covid vaccines are expected to contain only mRNA. However, it has been proven that the vaccines contain considerable amounts of DNA and other substances that should not be present. There is no doubt about it now. DNA can enter human cells very easily, regardless of length, and can get into cells everywhere. When DNA gets in the center of an important gene, the important gene will stop functioning. One problem is that the mRNA vaccine of Pfizer contains a promoter sequence of the cancer virus called SV40. This sequence could enter the human genome, and awakens and activates dormant carcinogenic genes. As a result, the risk of developing cancer increases. mRNA vaccines increase the risk of developing cancer while suppressing the immunity. Vaccination increases the risk of developing cancer dramatically compared to the unvaccinated state. The more people get vaccinated, the more people will probably get cancer. Vaccines appear to increase the risk of all types of cancers. There is credible information that the number of leukemia cases is on the rise. Vaccination causes the promoter sequence of the cancer virus to enter white blood cells and attach to red blood cells everywhere. As a result, more and more leukemia cases are reported. A lot of spikes of mRNA are produced. The spikes would be most protected from destruction. Possibly, long spike genes remain intact. So, if the long spike genes remain there, gene expression will continue to take place all the time. That is, spikes are generated forever. Once the DNA gets into the stem cells, the DNA will keep creating more and more spikes. As a result, IgG4 antibodies are induced. The number of spike-producing cells will not decrease, and it becomes impossible to get rid of spike-producing cells. As a results, It becomes normal for spikes to be present in cells. The produced spikes then flow into the bloodstream and cause a variety of health problems. So, any vaccine that induces IgG4 is deemed as a defective vaccine, and should no longer be produced. Normally, cancer cells are born and grow slowly. However, the vaccine suppresses the immunity, which makes it easier for cancer cells to grow. The vaccines cause turbo cancers. Suppression of the immunity is a major factor of turbo cancers. The increase in IgG4 antibodies results in suppression of cancer immunity. The more DNA the vaccine contains, the more intense the inflammation caused by the vaccine becomes. DNA is a foreign substance to the cells. So, DNA causes a severe reaction and kills the immune system of the cells. The more DNA the vaccine contains, the more severe the side effects caused by the vaccine become. Vaccines could contain many different impurities, but one possibility could be DNA. In the first place, DNA is something that should not be put into cells of your body.
6:34

Professor Emeritus Yasufumi Murakami of Tokyo University of Science: "It is almost certain that vaccines are contaminated with DNA. mRNA vaccines containing the DNA causes turbo cancers." Professor Murakami explains the mechanism of turbo cancers: The covid vaccines are expected to contain only mRNA. However, it has been proven that the vaccines contain considerable amounts of DNA and other substances that should not be present. There is no doubt about it now. DNA can enter human cells very easily, regardless of length, and can get into cells everywhere. When DNA gets in the center of an important gene, the important gene will stop functioning. One problem is that the mRNA vaccine of Pfizer contains a promoter sequence of the cancer virus called SV40. This sequence could enter the human genome, and awakens and activates dormant carcinogenic genes. As a result, the risk of developing cancer increases. mRNA vaccines increase the risk of developing cancer while suppressing the immunity. Vaccination increases the risk of developing cancer dramatically compared to the unvaccinated state. The more people get vaccinated, the more people will probably get cancer. Vaccines appear to increase the risk of all types of cancers. There is credible information that the number of leukemia cases is on the rise. Vaccination causes the promoter sequence of the cancer virus to enter white blood cells and attach to red blood cells everywhere. As a result, more and more leukemia cases are reported. A lot of spikes of mRNA are produced. The spikes would be most protected from destruction. Possibly, long spike genes remain intact. So, if the long spike genes remain there, gene expression will continue to take place all the time. That is, spikes are generated forever. Once the DNA gets into the stem cells, the DNA will keep creating more and more spikes. As a result, IgG4 antibodies are induced. The number of spike-producing cells will not decrease, and it becomes impossible to get rid of spike-producing cells. As a results, It becomes normal for spikes to be present in cells. The produced spikes then flow into the bloodstream and cause a variety of health problems. So, any vaccine that induces IgG4 is deemed as a defective vaccine, and should no longer be produced. Normally, cancer cells are born and grow slowly. However, the vaccine suppresses the immunity, which makes it easier for cancer cells to grow. The vaccines cause turbo cancers. Suppression of the immunity is a major factor of turbo cancers. The increase in IgG4 antibodies results in suppression of cancer immunity. The more DNA the vaccine contains, the more intense the inflammation caused by the vaccine becomes. DNA is a foreign substance to the cells. So, DNA causes a severe reaction and kills the immune system of the cells. The more DNA the vaccine contains, the more severe the side effects caused by the vaccine become. Vaccines could contain many different impurities, but one possibility could be DNA. In the first place, DNA is something that should not be put into cells of your body.

You

574,563 görüntüleme • 2 yıl önce

Dana White did an 86-hour water fast, and he says it changed how he sees his body. He went in after learning about Boston studies on prolonged water fasting. According to him, after 72+ hours your body starts shedding dead cells, generating new ones, and fighting inflammation and disease. He came out shredded with insane mental clarity and described hitting a zen-like euphoric state. Research shows that autophagy (cellular cleanup) significantly ramps up between 48-72 hours of fasting. Studies, including recent multi-day water fast trials, have found widespread shifts in thousands of proteins affecting metabolism, inflammation, immune function, and even brain-supporting structures. In a world of constant eating and processed food, strategic extended fasting is one of the most powerful (and free) ways to trigger deep biological repair mechanisms our bodies evolved with. Have you ever tried a multi-day fast, or does 72 hours sound insane to you?
2:56

Dana White did an 86-hour water fast, and he says it changed how he sees his body. He went in after learning about Boston studies on prolonged water fasting. According to him, after 72+ hours your body starts shedding dead cells, generating new ones, and fighting inflammation and disease. He came out shredded with insane mental clarity and described hitting a zen-like euphoric state. Research shows that autophagy (cellular cleanup) significantly ramps up between 48-72 hours of fasting. Studies, including recent multi-day water fast trials, have found widespread shifts in thousands of proteins affecting metabolism, inflammation, immune function, and even brain-supporting structures. In a world of constant eating and processed food, strategic extended fasting is one of the most powerful (and free) ways to trigger deep biological repair mechanisms our bodies evolved with. Have you ever tried a multi-day fast, or does 72 hours sound insane to you?

Camus

723,566 görüntüleme • 2 ay önce