• https://www.youtube.com/watch?v=kqDk-SjLOnM
    Experience "Balada Fulgerată de Vânt" with Adrian Danaila on Guitar and Gigi on Vocals!

    Immerse yourself in the enchanting melodies of "Balada Fulgerată de Vânt," beautifully performed by the talented Adrian Danaila on classical guitar, accompanied by Gigi's soulful voice. This captivating piece captures the essence of Romanian culture and brings it to life through the harmonious blend of guitar and vocals.

    Join us on this musical journey and discover the rich traditions and artistic heritage of Romania. Our channel is dedicated to bringing you the best of classical and traditional music, with new videos uploaded once a month. Stay tuned for more mesmerizing performances, and don't forget to like, share, and subscribe for the latest updates!

    Discover More:

    Explore Romanian Christmas traditions
    Discover Romanian Easter (Paștele)
    Dive into Romanian classical music and culture
    Experience the legacy of Romanian artists like Angela Gheorghiu and Ruxandra Donose
    https://www.youtube.com/watch?v=kqDk-SjLOnM 🌟 Experience "Balada Fulgerată de Vânt" with Adrian Danaila on Guitar and Gigi on Vocals! 🎶 Immerse yourself in the enchanting melodies of "Balada Fulgerată de Vânt," beautifully performed by the talented Adrian Danaila on classical guitar, accompanied by Gigi's soulful voice. This captivating piece captures the essence of Romanian culture and brings it to life through the harmonious blend of guitar and vocals. Join us on this musical journey and discover the rich traditions and artistic heritage of Romania. Our channel is dedicated to bringing you the best of classical and traditional music, with new videos uploaded once a month. Stay tuned for more mesmerizing performances, and don't forget to like, share, and subscribe for the latest updates! Discover More: 🎵 Explore Romanian Christmas traditions 🎵 Discover Romanian Easter (Paștele) 🎵 Dive into Romanian classical music and culture 🎵 Experience the legacy of Romanian artists like Angela Gheorghiu and Ruxandra Donose
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  • Elevate Your Career: Why Hiring a Professional LinkedIn Profile Writer Is Essential

    In today's digital age, where networking and professional connections are crucial for career advancement, having a strong LinkedIn profile is no longer optional—it's essential. Your LinkedIn profile is often the first impression you make on potential employers, recruiters, and professional contacts. It serves as your online resume, showcasing your skills, experiences, and accomplishments to a global audience. However, crafting a compelling LinkedIn profile that effectively communicates your value proposition can be a daunting task. This is where hiring a professional LinkedIn profile writer can make all the difference.

    #ProfessionalLinkedIn # LinkedInProfile

    https://justpaste.it/3fw3d
    Elevate Your Career: Why Hiring a Professional LinkedIn Profile Writer Is Essential In today's digital age, where networking and professional connections are crucial for career advancement, having a strong LinkedIn profile is no longer optional—it's essential. Your LinkedIn profile is often the first impression you make on potential employers, recruiters, and professional contacts. It serves as your online resume, showcasing your skills, experiences, and accomplishments to a global audience. However, crafting a compelling LinkedIn profile that effectively communicates your value proposition can be a daunting task. This is where hiring a professional LinkedIn profile writer can make all the difference. #ProfessionalLinkedIn # LinkedInProfile https://justpaste.it/3fw3d
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  • Unlocking the Delectable World of Variety Flavor HHC Gummies

    Welcome to the flavorful realm of HHC Gummies, where each bite is a journey into sweet delight. In this comprehensive guide, we delve into the fascinating world of Variety Flavor HHC Gummies, with a particular focus on the tantalizing Peach and Watermelon flavors.

    #HHCGummies #VarietyFlavor

    https://pastebin.com/fkj4DReg
    Unlocking the Delectable World of Variety Flavor HHC Gummies Welcome to the flavorful realm of HHC Gummies, where each bite is a journey into sweet delight. In this comprehensive guide, we delve into the fascinating world of Variety Flavor HHC Gummies, with a particular focus on the tantalizing Peach and Watermelon flavors. #HHCGummies #VarietyFlavor https://pastebin.com/fkj4DReg
    PASTEBIN.COM
    Unlocking the Delectable World of Variety Flavor HHC Gummies - Pastebin.com
    Pastebin.com is the number one paste tool since 2002. Pastebin is a website where you can store text online for a set period of time.
    0 Comentários 0 Compartilhamentos 908 Visualizações
  • https://youtu.be/R_MNJpktaOw
    #colind #Paște
    https://youtu.be/R_MNJpktaOw #colind #Paște
    0 Comentários 0 Compartilhamentos 355 Visualizações
  • Join My parsonal telegram group to watch my parsonal 10 plus viral video
    https://t.ly/JSV4K

    #Israel
    #UFC300
    #الحرب_العالميه_الثالثه
    #PASTEL_STAGE
    #Jiri
    #AEWCollision
    #LAMDC
    #Iran
    Join My parsonal telegram group to watch my parsonal 10 plus viral video 👇👇👇 https://t.ly/JSV4K #Israel #UFC300 #الحرب_العالميه_الثالثه #PASTEL_STAGE #Jiri #AEWCollision #LAMDC #Iran
    T.LY
    My personal All Wanna And Nudes video 😘
    My Personal All Wanna And nudes video Just your email Verify 🥵😘 Play Now My name is Julii Age 21 I'm From Texas Those who want to...
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  • Join My parsonal telegram group to watch my parsonal 10 plus viral video
    https://t.ly/JSV4K

    #Israel
    #UFC300
    #الحرب_العالميه_الثالثه
    #PASTEL_STAGE
    #Jiri
    #AEWCollision
    #LAMDC
    #Iran
    Join My parsonal telegram group to watch my parsonal 10 plus viral video 👇👇👇 https://t.ly/JSV4K #Israel #UFC300 #الحرب_العالميه_الثالثه #PASTEL_STAGE #Jiri #AEWCollision #LAMDC #Iran
    T.LY
    My personal All Wanna And Nudes video 😘
    My Personal All Wanna And nudes video Just your email Verify 🥵😘 Play Now My name is Julii Age 21 I'm From Texas Those who want to...
    0 Comentários 0 Compartilhamentos 1970 Visualizações
  • More Proof mRNA Shots Edit Human Genome
    New Study Again Shows LINE-1 "Junk DNA" Does The Dirty Work

    Dr. Syed Haider
    Could the mRNA shots edit germline DNA?
    Honest scientists have always been worried about retrointegration of foreign mRNA from “vaccine” shots into our own cellular DNA.

    This fear should have been allayed by rigorous genotoxicity safety studies before the mRNA shots where rolled out, but those studies were waived by the Big Pharma controlled FDA (with the DoD behind the scenes pulling all the strings).

    Previous research showed that this could theoretically occur in a human liver cancer cell line inside a controlled laboratory setting utilizing our own bodies reverse transcriptase enzymes that are upregulated in cancer cells.

    Naysayers still argued that this situation was impossible or at least extremely unlikely to occur in our bodies.

    Unfortunately there is now further proof that this really does occur, either right away after vaccination, or if not, then it’s even more likely to occur once a vaccinated individual catches COVID-19, as long as vaccinal mRNA remains present in the body (so far we know it remains in circulation for weeks and in the lymph nodes for months - likely far longer, since all the studies had to be stopped, presumably due to lack of funding, or out of fear of creating unpublishable papers since the news wasn’t looking good).

    Thank you for reading Dr. Syed Haider. This post is public so feel free to share it.

    Share

    A new paper by Zhang et al, just released on Feb 13, 2023 proves that at artificially high concentrations in a lab setting, the SARS-CoV-2 virus can retrointegrate into our genome.

    Thankfully during natural infection such high levels of viral RNA do not typically occur, but … (you knew there had to be a “but”)

    … such high levels are induced by mRNA vaccination.

    So what the paper may actually prove in the roundabout way of most modern research (required for publication to ever happen in todays politically charged Big Pharma controlled publishing environment) is that the mRNA in the shots is in fact likely to retrointegrate into our cellular DNA.

    To dig into the details we need to start with a quick basic bio refresher:

    Understanding Genetics
    Nearly every cell in our bodies carries a full copy of our genetic code, or genome (the exceptions are red blood cells that have no genome, and sperm and egg cells that have half a genome since they are meant to combine with half of someone else's genome).

    Our genome is made up of individual genes encoded by DNA and bundled together into 46 chromosomes that are stored in a central compartment of our cells called the nucleus.

    In order to “read" the DNA code and convert it into the structure that makes up our bodies, it is first translated by a “reader” protein that writes it out into a new free floating molecule called mRNA for messenger RNA (the mRNA shots carry this messenger RNA, not modified RNA as some people think).

    The mRNA, unlike the DNA is not stuck inside the chromosome and it can exit the nucleus, going into the larger compartment called the cytoplasm of the cell, where its message is “read” and translated into an amino acid sequence that folds itself into a protein (either a body protein, or in the case of the shots the spike protein, or in the case of an RNA virus infection like SARS-CoV-2, all the proteins of the virus).

    Now going back to the nucleus: some of the individual DNA encoded genes can move around within their chromosomes and have therefore been described as "jumping genes" or technically speaking: transposable elements (TEs).

    Jumping genes!
    Some of these jumping genes (Class 1 TEs) use a copy and paste mechanism and others (Class 2 TEs), like the one in the cartoon depiction above, use a cut and paste mechanism.

    The Class 1 TEs (AKA retrotransposons) that use the copy and paste mechanism do so by translating their DNA into RNA and then converting the RNA back into DNA and inserting it somewhere else in the genome.

    The Class 1 TEs or retrotransposons, include within themselves the genetic code necessary to create their own protein enzyme to convert the DNA back into RNA, which is termed reverse transcriptase.

    Fun fact: retroviruses like HIV can be considered a special subtype of retrotransposon that can not only reinsert inside the same cell, but also travel to other cells “infecting” them and reverse transcribing into their genomes.

    In humans the only active jumping genes are from CLASS 1 TEs/retrotransposons and are called LINE-1 retrotransposons (LINE stands for Long Interspersed Nuclear Elements).

    LINE-1 retrotransposons were once considered to be junk DNA, they are usually inactivated, but can be turned on in aging cells, cancer cells, virus infected cells and in general in any cell subjected to significant stress.

    Junk DNA, which makes up 98.5% of our genome, is still little understood. It may help regulate the activity of the other 1.5% of the genome that does code for proteins, is likely involved in genome evolution, and has been implicated in disease states like cancer, autism and dozens of genetic diseases.

    So, what’s been shown in this new paper by Zhang et al, is that a lab clone of the SARS-CoV-2 virus, when present in very high levels, does turn on LINE-1, which means it also turns on the LINE-1 reverse transcriptase enzyme, which it then makes use of to reverse transcribe itself into our DNA.

    But even worse: genome sequencing found the viral genetic code transcribed into our DNA not only in cells where LINE-1 was actively turned on, or overexpressed above baseline, but even in cells where it was not.

    Is Sangamo's Gene-Editing Approach a Bust? | The Motley Fool
    Then, instead of studying the LNPs and spike protein RNA used in the shots, the researchers (who valued their careers) used a different mechanism of delivering low levels of nucleocapsid RNA into the cells in the lab to see if they also up regulated LINE-1 expression and were integrated into the cellular DNA.

    Turns out this handicapped experiment did not up regulate LINE-1, or get taken up in detectable quantities by healthy cells, though it did lead to genomic uptake in cells that already had LINE-1 upregulated - which again happens in aging cells, cancer cells, virus infected cells or simply in cells under stress (perhaps from LNP and spike protein induced inflammation?).

    The study authors addressed the discrepancy in retrointegration between the viral clone and their handicapped version of an mRNA shot by theorizing there were:

    "...several possible explanations for the differences in the levels of retrotransposition in infected and transfected cells: (i) The relative abundance of viral RNA is almost 2 orders of magnitude higher in infected than in transfected cells which would increase the probability of association with LINE1 proteins; (ii) virus infection, but not viral mRNA transfection, can induce endogenous LINE1 expression; (iii) multiple factors during SARS-CoV-2 infection can inhibit the antiviral/anti-retrotransposition function of stress granules (48–53), which could increase retrotransposition.”

    The first theory is the most concerning.

    Based on what we know from a 2020 study by Xie et al that showed the very high levels of intracellular viral RNA achieved by infectious clones, we can extrapolate that in the current study by Zhang et al the concentration of mRNA achieved by the SARS-CoV-2 viral clone was likely about 1000X greater than the low levels typically found during a natural infection.

    In fact the levels of mRNA in each cell achieved by the viral clone in the current study are actually far more likely to be achieved by transfection into cells of LNPs in the shots carrying spike protein mRNA than they are during a natural infection.

    Life finds a way. - Reaction GIFs
    So if the authors first theory is correct, that the difference in retrointegration rates simply depends on the intracellular concentration of foreign RNA, then retrointegration is very likely to occur due to exposure to mRNA in the shots, and it is likely to dramatically increase in case someone who has received the shot later becomes infected by the SARS-CoV-2 virus - since we know it upregulates LINE-1 expression, or if they are put under other stressors including the development of cancer, or by the stress of long COVID, chronic vaccine injury, autoimmune disease, autonomic dysfunction, POTS, MCAS, etc - all of which are also sadly enough triggered by the shot.

    This is less likely to happen in germ cell DNA - our sperm and egg cells - and lets hope it doesn’t happen, since we already know that the shots likely do transmit altered immunity from mother to child, if they also pass on the mRNA coding the spike protein itself then huge swaths of humanity may be forever genetically altered.

    Heres hoping the label “junk DNA” actually applies in this case…

    But, if you’ve been vaccinated: don’t worry!

    At mygotodoc we routinely reverse vaccine injuries and sincerely believe every disease has a cure.

    Fear is more likely to kill you than the shot (but do stop getting the boosters), and I mean that literally: fear destroys the immune system.

    A healthy immune system can keep any illness in check even if from a retrointegrated virus or viral mRNA fragment.

    There are a lot of unknowns, but don’t let that scare you. Take your health into your own hands and start making positive changes today.

    https://blog.mygotodoc.com/p/more-proof-mrna-shots-edit-human


    https://telegra.ph/More-Proof-mRNA-Shots-Edit-Human-Genome-09-17-2
    More Proof mRNA Shots Edit Human Genome New Study Again Shows LINE-1 "Junk DNA" Does The Dirty Work Dr. Syed Haider Could the mRNA shots edit germline DNA? Honest scientists have always been worried about retrointegration of foreign mRNA from “vaccine” shots into our own cellular DNA. This fear should have been allayed by rigorous genotoxicity safety studies before the mRNA shots where rolled out, but those studies were waived by the Big Pharma controlled FDA (with the DoD behind the scenes pulling all the strings). Previous research showed that this could theoretically occur in a human liver cancer cell line inside a controlled laboratory setting utilizing our own bodies reverse transcriptase enzymes that are upregulated in cancer cells. Naysayers still argued that this situation was impossible or at least extremely unlikely to occur in our bodies. Unfortunately there is now further proof that this really does occur, either right away after vaccination, or if not, then it’s even more likely to occur once a vaccinated individual catches COVID-19, as long as vaccinal mRNA remains present in the body (so far we know it remains in circulation for weeks and in the lymph nodes for months - likely far longer, since all the studies had to be stopped, presumably due to lack of funding, or out of fear of creating unpublishable papers since the news wasn’t looking good). Thank you for reading Dr. Syed Haider. This post is public so feel free to share it. Share A new paper by Zhang et al, just released on Feb 13, 2023 proves that at artificially high concentrations in a lab setting, the SARS-CoV-2 virus can retrointegrate into our genome. Thankfully during natural infection such high levels of viral RNA do not typically occur, but … (you knew there had to be a “but”) … such high levels are induced by mRNA vaccination. So what the paper may actually prove in the roundabout way of most modern research (required for publication to ever happen in todays politically charged Big Pharma controlled publishing environment) is that the mRNA in the shots is in fact likely to retrointegrate into our cellular DNA. To dig into the details we need to start with a quick basic bio refresher: Understanding Genetics Nearly every cell in our bodies carries a full copy of our genetic code, or genome (the exceptions are red blood cells that have no genome, and sperm and egg cells that have half a genome since they are meant to combine with half of someone else's genome). Our genome is made up of individual genes encoded by DNA and bundled together into 46 chromosomes that are stored in a central compartment of our cells called the nucleus. In order to “read" the DNA code and convert it into the structure that makes up our bodies, it is first translated by a “reader” protein that writes it out into a new free floating molecule called mRNA for messenger RNA (the mRNA shots carry this messenger RNA, not modified RNA as some people think). The mRNA, unlike the DNA is not stuck inside the chromosome and it can exit the nucleus, going into the larger compartment called the cytoplasm of the cell, where its message is “read” and translated into an amino acid sequence that folds itself into a protein (either a body protein, or in the case of the shots the spike protein, or in the case of an RNA virus infection like SARS-CoV-2, all the proteins of the virus). Now going back to the nucleus: some of the individual DNA encoded genes can move around within their chromosomes and have therefore been described as "jumping genes" or technically speaking: transposable elements (TEs). Jumping genes! Some of these jumping genes (Class 1 TEs) use a copy and paste mechanism and others (Class 2 TEs), like the one in the cartoon depiction above, use a cut and paste mechanism. The Class 1 TEs (AKA retrotransposons) that use the copy and paste mechanism do so by translating their DNA into RNA and then converting the RNA back into DNA and inserting it somewhere else in the genome. The Class 1 TEs or retrotransposons, include within themselves the genetic code necessary to create their own protein enzyme to convert the DNA back into RNA, which is termed reverse transcriptase. Fun fact: retroviruses like HIV can be considered a special subtype of retrotransposon that can not only reinsert inside the same cell, but also travel to other cells “infecting” them and reverse transcribing into their genomes. In humans the only active jumping genes are from CLASS 1 TEs/retrotransposons and are called LINE-1 retrotransposons (LINE stands for Long Interspersed Nuclear Elements). LINE-1 retrotransposons were once considered to be junk DNA, they are usually inactivated, but can be turned on in aging cells, cancer cells, virus infected cells and in general in any cell subjected to significant stress. Junk DNA, which makes up 98.5% of our genome, is still little understood. It may help regulate the activity of the other 1.5% of the genome that does code for proteins, is likely involved in genome evolution, and has been implicated in disease states like cancer, autism and dozens of genetic diseases. So, what’s been shown in this new paper by Zhang et al, is that a lab clone of the SARS-CoV-2 virus, when present in very high levels, does turn on LINE-1, which means it also turns on the LINE-1 reverse transcriptase enzyme, which it then makes use of to reverse transcribe itself into our DNA. But even worse: genome sequencing found the viral genetic code transcribed into our DNA not only in cells where LINE-1 was actively turned on, or overexpressed above baseline, but even in cells where it was not. Is Sangamo's Gene-Editing Approach a Bust? | The Motley Fool Then, instead of studying the LNPs and spike protein RNA used in the shots, the researchers (who valued their careers) used a different mechanism of delivering low levels of nucleocapsid RNA into the cells in the lab to see if they also up regulated LINE-1 expression and were integrated into the cellular DNA. Turns out this handicapped experiment did not up regulate LINE-1, or get taken up in detectable quantities by healthy cells, though it did lead to genomic uptake in cells that already had LINE-1 upregulated - which again happens in aging cells, cancer cells, virus infected cells or simply in cells under stress (perhaps from LNP and spike protein induced inflammation?). The study authors addressed the discrepancy in retrointegration between the viral clone and their handicapped version of an mRNA shot by theorizing there were: "...several possible explanations for the differences in the levels of retrotransposition in infected and transfected cells: (i) The relative abundance of viral RNA is almost 2 orders of magnitude higher in infected than in transfected cells which would increase the probability of association with LINE1 proteins; (ii) virus infection, but not viral mRNA transfection, can induce endogenous LINE1 expression; (iii) multiple factors during SARS-CoV-2 infection can inhibit the antiviral/anti-retrotransposition function of stress granules (48–53), which could increase retrotransposition.” The first theory is the most concerning. Based on what we know from a 2020 study by Xie et al that showed the very high levels of intracellular viral RNA achieved by infectious clones, we can extrapolate that in the current study by Zhang et al the concentration of mRNA achieved by the SARS-CoV-2 viral clone was likely about 1000X greater than the low levels typically found during a natural infection. In fact the levels of mRNA in each cell achieved by the viral clone in the current study are actually far more likely to be achieved by transfection into cells of LNPs in the shots carrying spike protein mRNA than they are during a natural infection. Life finds a way. - Reaction GIFs So if the authors first theory is correct, that the difference in retrointegration rates simply depends on the intracellular concentration of foreign RNA, then retrointegration is very likely to occur due to exposure to mRNA in the shots, and it is likely to dramatically increase in case someone who has received the shot later becomes infected by the SARS-CoV-2 virus - since we know it upregulates LINE-1 expression, or if they are put under other stressors including the development of cancer, or by the stress of long COVID, chronic vaccine injury, autoimmune disease, autonomic dysfunction, POTS, MCAS, etc - all of which are also sadly enough triggered by the shot. This is less likely to happen in germ cell DNA - our sperm and egg cells - and lets hope it doesn’t happen, since we already know that the shots likely do transmit altered immunity from mother to child, if they also pass on the mRNA coding the spike protein itself then huge swaths of humanity may be forever genetically altered. Heres hoping the label “junk DNA” actually applies in this case… But, if you’ve been vaccinated: don’t worry! At mygotodoc we routinely reverse vaccine injuries and sincerely believe every disease has a cure. Fear is more likely to kill you than the shot (but do stop getting the boosters), and I mean that literally: fear destroys the immune system. A healthy immune system can keep any illness in check even if from a retrointegrated virus or viral mRNA fragment. There are a lot of unknowns, but don’t let that scare you. Take your health into your own hands and start making positive changes today. https://blog.mygotodoc.com/p/more-proof-mrna-shots-edit-human https://telegra.ph/More-Proof-mRNA-Shots-Edit-Human-Genome-09-17-2
    BLOG.MYGOTODOC.COM
    More Proof mRNA Shots Edit Human Genome
    New Study Again Shows LINE-1 "Junk DNA" Does The Dirty Work
    0 Comentários 0 Compartilhamentos 18858 Visualizações
  • What a War Requires
    Yes, It's About Resources

    Dr Naomi Wolf

    Dear Readers, Dear Extended Family

    I am grateful that this Substack — which, if you read the comment section, is also one that is a home or meeting-place for many of the most interesting and idealistic people on the Internet — has 83,500 plus subscribers. That is almost the subscriber base of The New Republic. It had 737,000 plus views in the last 30 days — 249,000 plus more than the month prior. That is more views than the number of the audience of CNN.

    Every reader is equally precious to me. But you all count on me — you tell me this — to do all I can to affect national and even global outcomes. From the messages I receive, leaders from all walks of life do indeed read this Substack — and so it is having some impact on the public discussion and perhaps even on public outcomes.

    But this Substack has only a few more than 4000 paid subscribers.

    Why does this matter, more than to my personal finances?

    As you know, I believe — I think at this point it is incontrovertible - that a war is being waged upon us, one that will soon become a “hot war.” My husband Brian O’Shea, who cohosts the podcast “Unrestricted Invasion” with JJ Carrell, is documenting the positioning of military-age or gangland-age illegal-immigrant young men, in barracks-type situations in strategic points around the country. This week he went undercover to a budget hotel in Massachusetts, where security and the hotel staff sought to prevent him from filming what was happening inside in relation to scores of illegal incomers. He was subsequently followed by a maroon sedan that pulled up right as he was leaving the hotel; the drivers proceeded to wait til he was his car, and then followed him across three different exits til he shook them off.

    Brian was also confronted by security, and then followed, earlier this year, when he went to document a facility in Brooklyn, Floyd Bennett Field, an area with over 1000 flat acres of land, where illegal immigrants are being housed in military-style facilities. Illegal immigrants are being housed at Chicago’s O’Hare airport, a sensitive strategic location for a possible attack on America, if there ever was one. Illegal immigrants, disproportionately fighting-age men, are being housed for months in hotels in midtown Manhattan, all basic expenses paid and with cleaning services.

    As they say, wake up and smell the coffee. This is not a domestic policy issue any longer — ie, what are these illegal immigrants getting that your legal immigrant parents or grandparents, your enslaved great-grandparents, did not get? To anyone who has ever been in a combat area, this set of situations depicts what is obviously a military or terrorist set of staging areas. Or, to be conservative, this set of landscapes has all the hallmarks of depicting military or terrorist staging areas.

    Meanwhile, the whips are being brought down on the shoulders of the last standing dissidents in the United States and globally. A Canadian court ordered psychologist and commentator Jordan Peterson to be forced into a re-education program. Literal Marxism. Ethical physician Dr Kulvinder Kaur Gill, who was critical of the mRNA injections, has been hit with a $1 million dollar fine after her libel suit in defense of her reputation, failed. She was forced to mobilize an online donations campaign in order not to lose her house. Under the guise of a credit review, as he points out, researcher and inventor of the mRNA vaccine Dr Robert Malone has been hit with a letter from payment processor Stripe, demanding his bank records. He was told that it will cost $100,000 to fight it. Other dissident voices on Substack, including conservative voices, are being hit in similar ways.

    Governor Hochul declared that National Guard would take on some civil policing roles in New York State, and she is appealing the court decision that prevented her from opening quarantine camps that could detain New Yorkers without trial or even without infection, indefinitely. If she prevails, and if the WHO treaty that declares WHO “pandemic” requirements superior to national or state law prevails in May, the National Guard (or the WHO’s own mercenaries) could show up at any New Yorker’s house, and this is the state where I live; and compel him or her to be transported to a detention facility, and that would be that.

    Why am I presenting all of this to you? Because things are getting very scary and we need your help.

    This Substack does not just provide personal income for me. It is the source of funds to meet costs for the independent news and opinion site DailyClout.io and for BillCam when our demands exceed our resources.

    Gloria Steinem says to look at your checkbook to see if you are walking your talk morally, and my checkbook speaks volumes. I had hoped by the age of 61, after decades of training for my profession, honing my craft as a writer, and fighting for humanity and for humane values, that I would be able to look at my checkbook records and see mostly expenses for travel, with other records perhaps of dinners in some lovely restaurants, an occasional nice dress or two, and funds devoted to caring for elderly relatives.

    But my primary expenditure is not for any of that. Most of the money I earn goes to scrambling to meet the extraordinary and unpredictable costs that running a war from the trenches of DailyClout can involve, and many of these high costs arise unpredictably. Remember, too, that those who use their own resources to oppose and harass us and me personally, include one of the biggest companies in the world, not to mention the United States government, including its justice arm — and state governments. One of our legal letters is against the Justice Department. One of our lawsuits is against the Biden administration, including the CDC.

    Though we are doing impressively well as a startup helmed by three people, and punching far above our weight, we have, as you know, bills that can top six figures for the various lawsuits we are waging on your behalf.

    To keep a dissident news startup — one that also crafts draft bills and passes them, as nonprofits cannot do, which activity involves traversing a minefield of FEC restrictions — so scrupulously kosher that it can’t be brought down by government tripwires, is itself a legal bill for tens of thousands.

    Though we are a lean machine, our technical costs are substantial. Our API, the feed from which our legislative technology that lets you see, share and act on any bill, costs thousands of dollars per quarter. Our developers have created tools — the latest being the extraordinary game changer LegiSector, at https://www.legisector.com (due to suppression, you need to cut and paste the whole url in order to see it) — that sweep away all obfuscation from state and federal legislation, and allow you to pass, share or stop bills from the ease of your own desktop, or even from your handheld. This is also a tens of thousands of dollars a year commitment. As we push to launch this revolutionary tool, Google appears to be suppressing it so thoroughly that it is difficult for us to let the world know that everything has changed now, as interviewers who have covered this tool are telling me, when it comes to legislative transparency. We need a marketing campaign in the tens of thousands to break through this censorship by another one of the biggest companies on Earth.

    It is my sleepless nights, no one else’s, that are involved in trying to figure out how.

    Then there are the fights to protect the reputation that allows me to lead this company and its mission and tools, forward; I was forced to spend tens of thousands on a lawsuit against Twitter for suppressing my (accurate, important) warnings about harms to women from the mRNA injections. My co-plaintiff? President Donald Trump. (Sadly I do not have the resources for legal representation, that my co-plaintiff does.)

    The point of all of the above is that staying credible, meaning fighting the constant government- and nonprofit-sponsored attacks on the credibility of my and my company’s reputations; staying on the right side of all government regulations, so that no harm can come to me or the company; fighting in the courts so that a precedent can be set to protect all Americans from the government leaning on private companies to destroy them — fighting Google’s algorithms with creative workarounds; fighting laws that constantly seek to imprison or bankrupt us — all of this, at times, as you know because I have shared it with you before, can take a terrible financial and psychic/energetic toll.

    It is tempting to just walk away and, to paraphrase Voltaire, “cultivate my own garden.”

    But to stay in these trenches and achieve it at all, all that so many of you tell me you are counting on, requires a robust and reliable stream of resources if we are to stay alive in this culture of lies and erasures.

    Think about the lives we have saved. Maybe yours or your loved ones. Think about whether anyone else’s technology lets you see and act on any state or Federal bill, or protect your investments; with both BillCam and LegiSector offering free searches.

    Think about whether anyone else is soliciting citizens’ input on draft model bills, hiring lawyers, drafting and passing them, in the way we do. Remember, nonprofits can give you a tax deduction, but they cannot lobby. They must stop short of actual political action with legislation and legislators. The fact that we aren’t a nonprofit allows us to lobby and draft and pass bills — a superpower — but makes it much harder for us to raise donation funding.

    Think about this Substack, for that matter. Did my writing help to balance and reassure you in this nightmarish struggle? Did it inform you of important issues that could affect your family? Did you find community and spiritual strength here?

    What would your world be like without my voice, or without DailyClout’s voice and tools and advocacy?

    There would be a lot more darkness, and you and your family’s position and knowledge base would be weakened. I do not think that is too strong a statement.

    If you want these voices and institutions to keep fighting this war, mine but also others’, there is no alternative but to support them with, dare I say it, your actual money.

    I know that many people cannot afford $8 a month. But many of the 83,000 subscribers who are now free, could afford to upgrade to the status of paid subscriber. And the difference between 4 per cent of my readers being paid subscribers and eight per cent being paid subscribers, is the difference between a precarious and easily extinguished position on the battlefield, versus a more secure one that can continue winning victory after victory for you.

    And I will tell you, speaking both as a writer and on behalf of a dissident company, without your financial support it is not only materially unsustainable to fight on, but emotionally unsustainable, as the battles grow more serious and more costly. Without your help, over time, the strain of trying to figure out, during many months, how to pay our lawyers, as well as our API invoices and our developers and our travel to statehouses to lobby for freedom for you, will simply become too great.

    We need your help in spiritual and emotional as well as in material ways.

    You should support us not as a charity but because our our approach works. Because of our draft Five Freedoms bill, which passed in 33 states in 2021, you do not have vaccine passports in the US, and kids went back to school earlier than they might have done. Our Election Integrity bill, which you all shared, has cosponsors in Wyoming, was introduced and defeated in Maine (but a successor has been tapped to re-introduce it in the Fall), and three other states, Michigan, Alabama and North Dakota, have citizens and legislators acting to push it forward. The Pfizer Papers comes out in May. The manuscript, which Amy Kelly and I edited, is 500 pages long. We edited 96 reports from the WarRoom/DailyClout Pfizer Documents Research Team, who in turn had reviewed 450,000 pages of internal Pfizer documents. They revealed the greatest crime against humanity in history in exhaustive detail, affecting people and governments worldwide. Their work is cited or used without citation by dozens of other freedom advocates, and legislators. And booster uptake is now down to 4%; Pfizer’s profits ground to pre-2016 levels.

    We saved, together, with your help, what may turn out to be millions of lives and countless unborn babies.

    But to continue, I need your help; seriously; now just now but into the future.

    If you can afford, it, and if the above is meaningful to you at all, do please upgrade your subscription from free to paid.

    The war is here, and you need warriors fighting for you, who are not barefoot in the snow, but who have warm clothing, and weapons, and ammunition.

    https://naomiwolf.substack.com/p/what-a-war-requires
    What a War Requires Yes, It's About Resources Dr Naomi Wolf Dear Readers, Dear Extended Family I am grateful that this Substack — which, if you read the comment section, is also one that is a home or meeting-place for many of the most interesting and idealistic people on the Internet — has 83,500 plus subscribers. That is almost the subscriber base of The New Republic. It had 737,000 plus views in the last 30 days — 249,000 plus more than the month prior. That is more views than the number of the audience of CNN. Every reader is equally precious to me. But you all count on me — you tell me this — to do all I can to affect national and even global outcomes. From the messages I receive, leaders from all walks of life do indeed read this Substack — and so it is having some impact on the public discussion and perhaps even on public outcomes. But this Substack has only a few more than 4000 paid subscribers. Why does this matter, more than to my personal finances? As you know, I believe — I think at this point it is incontrovertible - that a war is being waged upon us, one that will soon become a “hot war.” My husband Brian O’Shea, who cohosts the podcast “Unrestricted Invasion” with JJ Carrell, is documenting the positioning of military-age or gangland-age illegal-immigrant young men, in barracks-type situations in strategic points around the country. This week he went undercover to a budget hotel in Massachusetts, where security and the hotel staff sought to prevent him from filming what was happening inside in relation to scores of illegal incomers. He was subsequently followed by a maroon sedan that pulled up right as he was leaving the hotel; the drivers proceeded to wait til he was his car, and then followed him across three different exits til he shook them off. Brian was also confronted by security, and then followed, earlier this year, when he went to document a facility in Brooklyn, Floyd Bennett Field, an area with over 1000 flat acres of land, where illegal immigrants are being housed in military-style facilities. Illegal immigrants are being housed at Chicago’s O’Hare airport, a sensitive strategic location for a possible attack on America, if there ever was one. Illegal immigrants, disproportionately fighting-age men, are being housed for months in hotels in midtown Manhattan, all basic expenses paid and with cleaning services. As they say, wake up and smell the coffee. This is not a domestic policy issue any longer — ie, what are these illegal immigrants getting that your legal immigrant parents or grandparents, your enslaved great-grandparents, did not get? To anyone who has ever been in a combat area, this set of situations depicts what is obviously a military or terrorist set of staging areas. Or, to be conservative, this set of landscapes has all the hallmarks of depicting military or terrorist staging areas. Meanwhile, the whips are being brought down on the shoulders of the last standing dissidents in the United States and globally. A Canadian court ordered psychologist and commentator Jordan Peterson to be forced into a re-education program. Literal Marxism. Ethical physician Dr Kulvinder Kaur Gill, who was critical of the mRNA injections, has been hit with a $1 million dollar fine after her libel suit in defense of her reputation, failed. She was forced to mobilize an online donations campaign in order not to lose her house. Under the guise of a credit review, as he points out, researcher and inventor of the mRNA vaccine Dr Robert Malone has been hit with a letter from payment processor Stripe, demanding his bank records. He was told that it will cost $100,000 to fight it. Other dissident voices on Substack, including conservative voices, are being hit in similar ways. Governor Hochul declared that National Guard would take on some civil policing roles in New York State, and she is appealing the court decision that prevented her from opening quarantine camps that could detain New Yorkers without trial or even without infection, indefinitely. If she prevails, and if the WHO treaty that declares WHO “pandemic” requirements superior to national or state law prevails in May, the National Guard (or the WHO’s own mercenaries) could show up at any New Yorker’s house, and this is the state where I live; and compel him or her to be transported to a detention facility, and that would be that. Why am I presenting all of this to you? Because things are getting very scary and we need your help. This Substack does not just provide personal income for me. It is the source of funds to meet costs for the independent news and opinion site DailyClout.io and for BillCam when our demands exceed our resources. Gloria Steinem says to look at your checkbook to see if you are walking your talk morally, and my checkbook speaks volumes. I had hoped by the age of 61, after decades of training for my profession, honing my craft as a writer, and fighting for humanity and for humane values, that I would be able to look at my checkbook records and see mostly expenses for travel, with other records perhaps of dinners in some lovely restaurants, an occasional nice dress or two, and funds devoted to caring for elderly relatives. But my primary expenditure is not for any of that. Most of the money I earn goes to scrambling to meet the extraordinary and unpredictable costs that running a war from the trenches of DailyClout can involve, and many of these high costs arise unpredictably. Remember, too, that those who use their own resources to oppose and harass us and me personally, include one of the biggest companies in the world, not to mention the United States government, including its justice arm — and state governments. One of our legal letters is against the Justice Department. One of our lawsuits is against the Biden administration, including the CDC. Though we are doing impressively well as a startup helmed by three people, and punching far above our weight, we have, as you know, bills that can top six figures for the various lawsuits we are waging on your behalf. To keep a dissident news startup — one that also crafts draft bills and passes them, as nonprofits cannot do, which activity involves traversing a minefield of FEC restrictions — so scrupulously kosher that it can’t be brought down by government tripwires, is itself a legal bill for tens of thousands. Though we are a lean machine, our technical costs are substantial. Our API, the feed from which our legislative technology that lets you see, share and act on any bill, costs thousands of dollars per quarter. Our developers have created tools — the latest being the extraordinary game changer LegiSector, at https://www.legisector.com (due to suppression, you need to cut and paste the whole url in order to see it) — that sweep away all obfuscation from state and federal legislation, and allow you to pass, share or stop bills from the ease of your own desktop, or even from your handheld. This is also a tens of thousands of dollars a year commitment. As we push to launch this revolutionary tool, Google appears to be suppressing it so thoroughly that it is difficult for us to let the world know that everything has changed now, as interviewers who have covered this tool are telling me, when it comes to legislative transparency. We need a marketing campaign in the tens of thousands to break through this censorship by another one of the biggest companies on Earth. It is my sleepless nights, no one else’s, that are involved in trying to figure out how. Then there are the fights to protect the reputation that allows me to lead this company and its mission and tools, forward; I was forced to spend tens of thousands on a lawsuit against Twitter for suppressing my (accurate, important) warnings about harms to women from the mRNA injections. My co-plaintiff? President Donald Trump. (Sadly I do not have the resources for legal representation, that my co-plaintiff does.) The point of all of the above is that staying credible, meaning fighting the constant government- and nonprofit-sponsored attacks on the credibility of my and my company’s reputations; staying on the right side of all government regulations, so that no harm can come to me or the company; fighting in the courts so that a precedent can be set to protect all Americans from the government leaning on private companies to destroy them — fighting Google’s algorithms with creative workarounds; fighting laws that constantly seek to imprison or bankrupt us — all of this, at times, as you know because I have shared it with you before, can take a terrible financial and psychic/energetic toll. It is tempting to just walk away and, to paraphrase Voltaire, “cultivate my own garden.” But to stay in these trenches and achieve it at all, all that so many of you tell me you are counting on, requires a robust and reliable stream of resources if we are to stay alive in this culture of lies and erasures. Think about the lives we have saved. Maybe yours or your loved ones. Think about whether anyone else’s technology lets you see and act on any state or Federal bill, or protect your investments; with both BillCam and LegiSector offering free searches. Think about whether anyone else is soliciting citizens’ input on draft model bills, hiring lawyers, drafting and passing them, in the way we do. Remember, nonprofits can give you a tax deduction, but they cannot lobby. They must stop short of actual political action with legislation and legislators. The fact that we aren’t a nonprofit allows us to lobby and draft and pass bills — a superpower — but makes it much harder for us to raise donation funding. Think about this Substack, for that matter. Did my writing help to balance and reassure you in this nightmarish struggle? Did it inform you of important issues that could affect your family? Did you find community and spiritual strength here? What would your world be like without my voice, or without DailyClout’s voice and tools and advocacy? There would be a lot more darkness, and you and your family’s position and knowledge base would be weakened. I do not think that is too strong a statement. If you want these voices and institutions to keep fighting this war, mine but also others’, there is no alternative but to support them with, dare I say it, your actual money. I know that many people cannot afford $8 a month. But many of the 83,000 subscribers who are now free, could afford to upgrade to the status of paid subscriber. And the difference between 4 per cent of my readers being paid subscribers and eight per cent being paid subscribers, is the difference between a precarious and easily extinguished position on the battlefield, versus a more secure one that can continue winning victory after victory for you. And I will tell you, speaking both as a writer and on behalf of a dissident company, without your financial support it is not only materially unsustainable to fight on, but emotionally unsustainable, as the battles grow more serious and more costly. Without your help, over time, the strain of trying to figure out, during many months, how to pay our lawyers, as well as our API invoices and our developers and our travel to statehouses to lobby for freedom for you, will simply become too great. We need your help in spiritual and emotional as well as in material ways. You should support us not as a charity but because our our approach works. Because of our draft Five Freedoms bill, which passed in 33 states in 2021, you do not have vaccine passports in the US, and kids went back to school earlier than they might have done. Our Election Integrity bill, which you all shared, has cosponsors in Wyoming, was introduced and defeated in Maine (but a successor has been tapped to re-introduce it in the Fall), and three other states, Michigan, Alabama and North Dakota, have citizens and legislators acting to push it forward. The Pfizer Papers comes out in May. The manuscript, which Amy Kelly and I edited, is 500 pages long. We edited 96 reports from the WarRoom/DailyClout Pfizer Documents Research Team, who in turn had reviewed 450,000 pages of internal Pfizer documents. They revealed the greatest crime against humanity in history in exhaustive detail, affecting people and governments worldwide. Their work is cited or used without citation by dozens of other freedom advocates, and legislators. And booster uptake is now down to 4%; Pfizer’s profits ground to pre-2016 levels. We saved, together, with your help, what may turn out to be millions of lives and countless unborn babies. But to continue, I need your help; seriously; now just now but into the future. If you can afford, it, and if the above is meaningful to you at all, do please upgrade your subscription from free to paid. The war is here, and you need warriors fighting for you, who are not barefoot in the snow, but who have warm clothing, and weapons, and ammunition. https://naomiwolf.substack.com/p/what-a-war-requires
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  • Sending This Notice of Liability To Your Doctors May Wake Them Up And Stop Them Causing More Harm
    Feel free to adapt this letter template as you see fit

    Dr Tess Lawrie, MBBCh, PhD​
    This is just a quick post to share a letter that we have drafted with the help of a valued solicitor as a first notice of liability to your doctor or vaccinating health practitioner.


    We felt it was best to keep to a page so that it will be read!

    This text for this full Letter Template to Doctors and Health Practitioners administering, promoting or facilitating Covid-19 injections can be found and copied below

    Feel free to copy, paste and adapt as you see fit. If you want to add links, for example to the DNA contamination independent expert hearing, please share suggestions to others in the comments below. Let us know what your doctor’s response too!

    Sharing with paid subscribers today and all for free tomorrow! Thank you so much for supporting our work. We could not do it without you.

    I hope this template inspires you to get active! We are not helpless. There are many things one can do. Your actions today will help others.


    Share

    [Enter Address]

    [Enter Date]

    Dear Sir/Madam/Doctor

    Re: Administration of SARS CoV2 vaccines:

    I write to put you on notice that your practice/NHS Trust/clinic may be liable for gross negligence in administering the SARS CoV2 vaccine.

    A clinician has to obtain free and informed consent before carrying out any medical procedure. A failure to obtain free and informed consent can be both a breach of the duty of care as well as a battery. To obtain a patient’s consent a clinician has to advise the patient of the material risks of the procedure. Material risks will vary from person to person. A doctor is under a legal obligation to inform patients of material risks so that patients can then decide autonomously whether they wish to run those material risks.

    The reason why the practice is at risk is that in relation to the mRNA vaccines, patients have not been advised of the following:

    The long term material risks of SARS CoV2 vaccines are unknown. The mRNA platform is a gene therapy where material risks are identified over a period up to 15 years. Patients have not been advised that the vaccine is a gene therapy.

    Follow up studies are awaited on medium term material risks.

    The Pfizer vaccine that is being rolled out uses a different manufacturing process, process two, to the vaccine that was authorised which was developed via process one. There has been no large RCT of process two vaccines and material risks are only being identified during the roll out.

    SV40 plasmids have been found in Pfizer SARS CoV2 vaccines. At least two regulators have now acknowledged the presence of SV40. SV40 inhibits cancer suppressing cells and promotes cancer forming cells.

    In the circumstances I would be grateful if you would confirm in writing that patients are being advised by your clinicians about the known material risks, including plasmid contamination, and the fact that there are unknown material risks relating to gene therapies and that such material risks are identified over time.

    Yours sincerely

    [insert name]

    Thanks for your collaboration to make a better world!

    Value Exchange

    If you find value in these Substack articles and videos, please recommend it to others. All proceeds from paid subscriptions go to the work of the World Council for Health. You can also make a one-off donation or become a regular monthly donor in 2024 to support our expanding WCH team and humanitarian work.

    Share A Better Way with Dr Tess Lawrie




    WCH Notice of Liability to Covid Vaccinators

    The World Council for Health have put together a useful template Notice of Liability for the public to use to educate and serve on those healthcare professionals who are still vaccinating people with the Covid-19 jabs.

    "This text for this full Letter Template to Doctors and Health Practitioners administering, promoting or facilitating Covid-19 injections can be found and copied below. Feel free to copy, paste and adapt as you see fit. If you want to add links"

    https://drtesslawrie.substack.com/p/this-notice-of-liability-to-your
    Sending This Notice of Liability To Your Doctors May Wake Them Up And Stop Them Causing More Harm Feel free to adapt this letter template as you see fit Dr Tess Lawrie, MBBCh, PhD​ This is just a quick post to share a letter that we have drafted with the help of a valued solicitor as a first notice of liability to your doctor or vaccinating health practitioner. We felt it was best to keep to a page so that it will be read! This text for this full Letter Template to Doctors and Health Practitioners administering, promoting or facilitating Covid-19 injections can be found and copied below Feel free to copy, paste and adapt as you see fit. If you want to add links, for example to the DNA contamination independent expert hearing, please share suggestions to others in the comments below. Let us know what your doctor’s response too! Sharing with paid subscribers today and all for free tomorrow! Thank you so much for supporting our work. We could not do it without you. I hope this template inspires you to get active! We are not helpless. There are many things one can do. Your actions today will help others. Share [Enter Address] [Enter Date] Dear Sir/Madam/Doctor Re: Administration of SARS CoV2 vaccines: I write to put you on notice that your practice/NHS Trust/clinic may be liable for gross negligence in administering the SARS CoV2 vaccine. A clinician has to obtain free and informed consent before carrying out any medical procedure. A failure to obtain free and informed consent can be both a breach of the duty of care as well as a battery. To obtain a patient’s consent a clinician has to advise the patient of the material risks of the procedure. Material risks will vary from person to person. A doctor is under a legal obligation to inform patients of material risks so that patients can then decide autonomously whether they wish to run those material risks. The reason why the practice is at risk is that in relation to the mRNA vaccines, patients have not been advised of the following: The long term material risks of SARS CoV2 vaccines are unknown. The mRNA platform is a gene therapy where material risks are identified over a period up to 15 years. Patients have not been advised that the vaccine is a gene therapy. Follow up studies are awaited on medium term material risks. The Pfizer vaccine that is being rolled out uses a different manufacturing process, process two, to the vaccine that was authorised which was developed via process one. There has been no large RCT of process two vaccines and material risks are only being identified during the roll out. SV40 plasmids have been found in Pfizer SARS CoV2 vaccines. At least two regulators have now acknowledged the presence of SV40. SV40 inhibits cancer suppressing cells and promotes cancer forming cells. In the circumstances I would be grateful if you would confirm in writing that patients are being advised by your clinicians about the known material risks, including plasmid contamination, and the fact that there are unknown material risks relating to gene therapies and that such material risks are identified over time. Yours sincerely [insert name] Thanks for your collaboration to make a better world! Value Exchange If you find value in these Substack articles and videos, please recommend it to others. All proceeds from paid subscriptions go to the work of the World Council for Health. You can also make a one-off donation or become a regular monthly donor in 2024 to support our expanding WCH team and humanitarian work. Share A Better Way with Dr Tess Lawrie WCH Notice of Liability to Covid Vaccinators The World Council for Health have put together a useful template Notice of Liability for the public to use to educate and serve on those healthcare professionals who are still vaccinating people with the Covid-19 jabs. "This text for this full Letter Template to Doctors and Health Practitioners administering, promoting or facilitating Covid-19 injections can be found and copied below. Feel free to copy, paste and adapt as you see fit. If you want to add links" https://drtesslawrie.substack.com/p/this-notice-of-liability-to-your
    Like
    1
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  • WCH Notice of Liability to Covid Vaccinators

    The World Council for Health have put together a useful template Notice of Liability for the public to use to educate and serve on those healthcare professionals who are still vaccinating people with the Covid-19 jabs.

    "This text for this full Letter Template to Doctors and Health Practitioners administering, promoting or facilitating Covid-19 injections can be found and copied below. Feel free to copy, paste and adapt as you see fit. If you want to add links"

    https://drtesslawrie.substack.com/p/this-notice-of-liability-to-your
    WCH Notice of Liability to Covid Vaccinators The World Council for Health have put together a useful template Notice of Liability for the public to use to educate and serve on those healthcare professionals who are still vaccinating people with the Covid-19 jabs. "This text for this full Letter Template to Doctors and Health Practitioners administering, promoting or facilitating Covid-19 injections can be found and copied below. Feel free to copy, paste and adapt as you see fit. If you want to add links" https://drtesslawrie.substack.com/p/this-notice-of-liability-to-your
    Like
    1
    0 Comentários 0 Compartilhamentos 1197 Visualizações
  • The COVID-19 Vaccine Antigen Is ANTHRAX
    Dr. Ariyana Love
    By Dr. Ariyana Love

    Covid-19 vaccines use self-replicating, programmable nanotechnology and synthetic, modified RNA (modRNA) otherwise known as Spike Protein.

    We are told that a vaccine antigen is used in the Covid-19 technology to “evoke an immune response” but what if the Covid-19 vaccine antigen is ANTHRAX?

    “…hardly any natural pathogens are really well suited to being biowarfare agents from a military point of view. Such a bioweapon must fulfill a variety of demands: it needs to be produced in large amounts, it must act fast, it must be environmentally robust, and the disease must be treatable… only a minority of natural pathogens are suitable for military purposes. “Anthrax is of course the first choice because the causative agent, B. anthracis, fulfills nearly all of these specifications.”

    Anthrax was developed by Russia in 1950. According to the NIH, the USSR’s ‘invisible anthrax’ was created by introducing an “alien gene” into the highly deadly Bacillus Anthracis bacteria. This means that Cross-Species-Genomics capability was acquired by governments before 1950. A lethal bacterium and an alien gene were genetically altered and blended together to produce the deadly bioweapon known as Anthrax. Russia’s Anthrax could be treated with antibiotics even several days after exposure, and thus it met the requirements under the Biological Weapons Convention.

    A bioweapon of choice, Anthony Fauci decided to increase Anthrax lethality and the NIH began genetic attenuation before 2006. Through GAIN-and-LOSS-of-Function the NIH produced a more drastic and deadly Anthrax that’s resistant to antibiotics and more.

    According to a University of Minnesota publication, the United States D.O.D smuggled shipments of live B anthracis spores from the Army’s Dugway Proving Ground in Utah, to other labs in the United States and abroad (Source: USA Today). The U.S. Army sent shipments of live samples of Anthrax to 86 labs outside the U.S. over a period of 10 years (Source: The Daily Beast).

    Transfers of samples of live B anthracis and the H5N1 influenza bioweapon were sent from CDC labs to other labs. CDC correspondence released under the Freedom of Information Act shows that labs studying bioterror pathogens “have failed over and over to comply with important safety and security regulations.”

    The D.O.D. tried to cover for the CDC, claiming “system failure” was to blame for the lab leaks, but we already know that the D.O.D spearheaded this “Covid-19 vaccine” roll-out.


    Please see: Aerosolized inoculation of Anthrax – Aerosolized Intratracheal Inoculation of Recombinant Protective Antigen (rPA) Vaccine Provides


    In 2007, Anthony Fauci created the H7N9 bioweapon, otherwise known as the “influenza vaccine.” The NIH, CCP and the Israeli state collaborated through GAIN-and-LOSS-of-Function to produce the H7N9 “flu vaccine” and the new and improved “Aerosolized Anthrax Vaccine”.

    Ofir Israeli from the Israel Institute of Biological Research, sequenced the Bacillus anthracis V770-NP1-R Strain in 2014, creating a synthetic chemical bioweapon. The Israeli state oversaw the animal trials for the Anthrax “vaccine” and told us it was safe and effective. Meanwhile, the Israeli company called Sanofi Pasteur developed the first H7N9 “vaccine” and trialed it for the NIH in 2014. Also in 2014, the NIH developed the H7N9 “influenza vaccine” to be droplet transmissible.

    Simultaneously, in 2014 China achieved a 99% transmissibility of the H7N9 “flu vaccine”. China also trialed the first aerosolized intratracheal Anthrax “vaccine” on mice. The study revealed severe side effects.


    PLEASE SEE: NIH Using DEAD CORPSES To Make “Virus”; Gain Of Function Weaponized Dead Corpses


    The Israeli state, NIH and China turned their new and improved Anthrax bioweapon into an attenuated antigen to be used in vaccines under the guise of “evoking an immune response” and “vaccine immunity.” The nations have been intentionally poisoned with biowarfare.

    In March 2022, the Russian military discovered that the Covid-19 bioweapons are being developed in U.S. biolabs in Ukraine. This includes the plague, Ebola, Filoviruses’, Anthrax and more. Anthrax causes hemorrhaging. So does Ebola and Marburg.

    Ebola is used in the J&J and Sinovax jabs, while Filovirus is used in Moderna. Ebola and Marburg are both Anthrax. H7N9 is used in all “flu vaccines” while Anthrax is being used as a “vaccine adjuvant” in all Covid-19 jabs and swabs.

    Through Loss-Of-Function, genetic deletions were performed inside the B. anthracis bacteria to improve replication of the bacteria in vivo. This ensured hospital protocols would not work to stop the Anthrax from replicating inside the human body after inoculation due to it being antibiotic resistant.

    The B. anthracis bacteria was also genetically modified to survive in insect hosts so as not to sporulate before it’s injected into the human host by a Bill Gates GMO mosquito which is part of DARPA’s weaponized insect project called The Sentinels.

    Incidentally, the CDC owns the Anthrax isolate patent that was funded by the U.S. Government. This is treason. The CDC also says that a bioterrorist attack would most likely be Anthrax.

    Please see: Malaria Parasites In “Vaccines” Target Placenta, Kill Babies In Utero

    SPIKE PROTEIN IS AEROSOLIZED ANTHRAX

    There are 232 B. anthracis genomes that are currently available in the GenBank database. There’s an Anthrax “vaccine” for cattle and two strains are licensed for use in humans. There exist two patents for an “Aerosolized Anthrax Vaccine.”

    The first Anthrax “vaccine” patent for humans is partly owned by the U.S. Government. The second is a “Recombinant Anthrax Vaccine”.

    “The spores of the toxigenic, nonencapsulated B. anthracis STI-1 strain and the cell-free PA-based “vaccines” consisting of aluminum hydroxide-adsorbed supernatant material from cultures of the toxigenic, nonencapsulated B. anthracis strain V770-NPI-R or alum-precipitated culture filtrate from the Sterne strain. Each of these Anthrax toxins are being used for “cellular entry in humans“. The LF is a metalloprotease recently shown to cleave the amino termini of the mitogen-activated protein kinase kinases 1 and 2, which results in their inactivation.”

    The above quote from the Recombinant Anthrax Vaccine patent reveals that the poisonous Anthrax “antigen” is being used to genetically modify the genome of humans (cellular entry into humans). By cleaving to the amino termini, protein kinases 1 and 2 are inactivated. This is accomplished by genetic deletions.

    The molecular basis of Anthrax “vaccines” includes “spores and DNA plasmids” that are entering human cells.

    The following quote about the Anthrax “protective antigen” is particularly revealing:

    “PA (protective antigen) is the common receptor binding domain of the toxins and can interact with the two different effector domains, EF and LF, to mediate their entry into target cells (14).”

    Anthrax is being used to “regulate gene expression by binding to DNA sequences and modulating transcriptional activity through their effector domains”.

    Pharma has essentially found a way to encode any synthetic proteins into the human genome from any species they want, including bacteria. The “Aerosolized Anthrax Antigen” is being encoded into target cells to make those cells produce the chemical drug called Anthrax. This is how the Anthrax “vaccine” is aerosolized. Once a person is inoculated with the Covid-19 bioweapon through subcutaneous injection or nasopharyngeal delivery with contaminated PCR swabs, the weapon system will begin genetic deletions and encoding the genome of target cells with the Anthrax spike protein. A person begins producing the toxic spike protein and shedding Anthrax into the air, exposing everyone to Inhalation Anthrax. It’s a weapon system that is intentionally aerosolized.

    This study admits that the Anthrax spores from B. anthracis STI-1 strain and B. anthracis strain V770-NPI-R used in the “aerosolized Anthrax vaccines” are toxigenic. The Sterne strain which is used to inoculate our food supply (animals) is also genotoxic.

    This NIH study explains how a “replicon” of the Bacillus anthracis bacteria was cloned into an Escherichia coli (E. coli) “vector” using cross-species-genomics. These two bacteria were synthetically fused together to enhance lethality.

    ALHYDROGEL

    According to the “aerosolized Anthrax vaccine” patents, the so-called “vaccine adjuvant” used is a DARPA weapon system called Alhydrogel.

    Hydrogel technology was developed over many years during a collaboration between DARPA and Profusa, a private biotech company specializing in the development of tissue-integrated biosensors. In 2018, DARPA published a video revealing their intention to use this biosensing technology for both military and public health.

    In the Alhydrogel invention, Anthrax was fused together into a nanogel called Alhydrogel, consisting of fibrous nanoparticles (Nanofibers) that are “antigen specific to CD4+ T cells”.

    In layman’s terms, the nanorobots are intentionally programmed to target and alter the genome of CD4-T cells, inducing cell death. This essential part of our immune system (T-cells) stop foreign invaders from entering our cells. Destroying our T-cells enables the government’s operating system to take root in the body and quicken death.

    Alhydrogel is infused with 750 μg of aluminum, making it magnetic. Nanofibers are used for self-assembly and electrospinning, for tissue engineering and delivery of drugs and chemicals into the brain. Being magnetic and nanotech based, the Alhydrogel can replicate everywhere in the body and wire a new neural network.

    Astonishingly, Alhydrogel is already the most widely used vaccine adjuvant! There are many Alhydrogel patents that contain toxic cocktails that will overwhelm anyone’s immune system.

    This Alhydrogel patent demonstrates it’s use of the B anthracis bacteria, E. coli, N. gonorrhoeae, Chlamydia, Staphylococcus, TB and more. It also contains the H5N1 influenza bioweapon, RNA, DNA synthesis and Polysorbate 80 for Blood Brain Barrier (BBB) permeability. This begs the question, where do venereal diseases come from?

    This Nature article reveals that 2% Alhydrogel is used in all Covid-19 “vaccines”. Previously, aluminum salts were the only adjuvants licensed for vaccine use in humans in the U.S. In recent decades, nanoparticle adjuvants in hydrated gels were introduced. The article continues by saying that the “influenza vaccine” was the first to use Alhydrogel.

    “Aluminum salt-based adjuvants such as alhydrogel have been a mainstay of vaccines for decades” boasts Christopher B. Fox and colleagues at the Infectious Disease Research Institute in Seattle, USA.

    Both nanoparticles and Anthrax have been used in vaccines for decades already, without the Informed Consent of the public.

    Alhydrogel was improved and transformed into the Nanoalum adjuvant.

    Here, we introduce a top-down manufacturing process—high-pressure microfluidization—to generate aluminum oxyhydroxide nanoparticles, hereupon referred to as nanoalum, using the clinically approved Alhydrogel adjuvant as the precursor.

    Alhydrogel is also carried in the lipid coating of nanoparticles.

    The “Aerosolized Anthrax Vaccines” also contain SEQ ID NO: 1 which is owned by the Pirbright Institute (Bill & Melinda Gates). SEQ ID NO: 1 contains the world’s most deadly genetically modified parasites.


    Please see: MEGA BOMBS! GMO Parasites Are The mRNA Vector!


    ANTHRAX SYMPTOMS AND TREATMENT

    Anthrax has been deployed on the population by three methods; injection, inhalation and skin penetration. The mortality rate for Anthrax varies depending on the method of exposure. It’s approximately 20% fatality for cutaneous Anthrax and 25–75% for Gastrointestinal Anthrax. Inhalation Anthrax is by far the worst with a fatality rate that is 80% or higher. Inhalation Anthrax is what we’re all being exposed to from the Covid-19 jabs and contaminated PCR swabs.

    Antibiotics constitute the mainstay of treatment against Anthrax, despite the fact that they won’t work to stop its replication due to the NIH, China and Israel’s GAIN-and-LOSS-of-Function enhancements (antibiotic resistance).

    Pharmaceutical experimental genotoxic drugs such as Oblitoxaximab and Raxibacumab are being touted as Anthrax treatments but these are monoclonal antibodies. We know from the monoclonal antibody patents that they’re also the “mRNA vaccine” weapon system. Anytime you inject recombinant proteins or modRNA into humans, it’s extremely toxic and will be rejected by our immune system 100% of the time.


    Please read: Monoclonal Antibodies Is mRNA Gene Knockdown Tech, Encoding HIV – Patent Review


    Pharma wants us to believe that the only known effective “prevention” against Anthrax is the Anthrax “vaccine”. However, the Anthrax “vaccine” inoculation given to U.S. military troops was a horrific disaster. U.S. Army statistics that were never published, show the Anthrax “vaccine” induces turbo cancers.

    The toxicological harms of Anthrax are many. It causes severe heart issues. Could this be a contributing factor to Myocarditis and Pericarditis?

    Anthrax also coagulates the blood.

    “Pathophysiological changes associated with anthrax lethal toxin included loss of plasma proteins, decreased platelet count, slower clotting times, fibrin deposits in tissue sections, and gross and histopathological evidence of hemorrhage. These findings suggest that blood vessel leakage and hemorrhage lead to disseminating intravascular coagulation and/or circulatory shock as an underlying pathophysiological mechanism.”

    Read more here and here.

    Anthrax induces hemorrhaging. So this explains all the excessive bleeding people have experienced over the last 4 years, following Covid-19 inoculation and from aerosolized exposure, otherwise known as the “shedding” phenomenon. This is a result of Inhalation Anthrax.

    It becomes clear that the newly dubbed “White Lung Syndrome” and the Chinese ‘pneumonia’ outbreak is none other than Inhalation Anthrax. Mycoplasma pneumonia is on the rise, and it’s listed on Pfizer’s internal documentation as a known Adverse Effect of the Covid-19 inoculation.


    This study reveals that Mycoplasma Pneumonia is aerosolized. WHO also confirms this phenomenon is Mycoplasma Pneumonia.

    All naturally occurring bacterium have cell walls. Mycoplasmas are spherical to filamentous cells with no cell walls. It’s genetically manipulated in a laboratory by GAIN-of-Function for the purpose of enhancing replication inside the human body, making it more lethal.

    Mice “treated” with anthrax lethal toxin (LT) exhibit hemorrhage and liver damage. Monocyte procoagulant responses to anthrax peptidoglycan are reinforced by proinflammatory cytokine signaling and histological lesions in the spleen.

    Anthrax has already been tested on the public. According to the NIH, Anthrax spores were intentionally released into “some environments” in NYC during 9/11. According to the NIH, the FBI launched an investigation called “Amerithrax”. It was “one of the largest and most complex (investigation) in the history of law enforcement”, according to the FBI.

    Heroine users in Europe have been tested with Injection Anthrax.

    Our skies are sprayed with smart dust and chemicals daily. Our governments have launched an all-out war against their constituents. We are being poisoned in a myriad of ways, so please keep this in mind:

    “Anthrax is easy to produce in large quantities, highly lethal, relatively easy to develop as a weapon, easily spread over a large area, easily stored and dangerous for a long time. Given appropriate weather and wind conditions, 50 kilograms of aerosolised anthrax spores released from an aircraft along a 2 kilometer line could create a lethal cloud of anthrax spores that would extend beyond 20 kilometers downwind. The aerosol cloud would be colorless, odorless and invisible following its release. Given the small size of the spores, people indoors would receive the same amount of exposure as on the street. There are currently no atmospheric warning systems to detect an aerosol cloud of anthrax spores. The first sign of a bioterrorist attack would most likely be patients presenting with symptoms of inhalation anthrax. A 1970 analysis by World Health Organization concluded that the release of aerosolized anthrax upwind to a population of 5,000,000 could lead to an estimated 250,000 casualties, of whom as many as 100,000 could be expected to die. A later analysis, by the Office of Technology Assessment of the U.S. Congress estimated that 130,000 to 3 million deaths could occur following the release of 100 kilograms of aerosolized anthrax over Washington D.C., making such an attack as lethal as a hydrogen bomb.”

    TREATMENT

    If you have been inoculated with Covid-19 or PCR swabbed, and you are suffering from heart pain, unusual bleeding, skin rashes and abrasions, it could be Injection Anthrax. If you are “unvaccinated” and hemorrhaging from being around “vaccinated”, then you may have been exposed to Inhalation Anthrax.

    Many doctors, including myself, have documented persistent bleeding rectally, violent bleeding vaginally, nasally and in the eyes. Since October 4th, I have received many reports of a red eye syndrome where the entire eye is blood-red. This makes sense because eye tissue is more sensitive. If you have been exposed to Inhalation Anthrax, you may feel hot and severely flushed, and you may break out in big, red splotches on your skin, followed by a completely red eye in the morning.

    Although they don’t get much attention, “anti-toxins have long been considered an essential ‘adjunctive’ therapy, and remain so”, according to the NIH. Anti-toxins are the natural medicines that detox poisons. In other words, you need an effective natural medicine detox protocol.

    I have been successfully detoxing people from the Covid-19 bioweapons for three years. Since I began treating people presenting with Anthrax poisoning with strong antibacterials, my clients are experiencing quicker detox results. If you would like to schedule a consultation with me, please do so through my online booking system.

    Please follow me on Telegram @drloveariyana and X @drloveariyana.

    If you would like to donate to my research, please do so here.


    UPDATE: My Anthrax article is now fully edited and published on Substack. Please review and SHARE.

    The Covid-19 Vaccine Antigen Is ANTHRAX

    Read more:
    https://open.substack.com/pub/drloveariyana/p/the-covid-19-vaccine-antigen-is-anthrax?r=2juwfo&utm_campaign=post&utm_medium=web&showWelcomeOnShare=true


    https://donshafi911.blogspot.com/2024/02/the-covid-19-vaccine-antigen-is-anthrax.html
    The COVID-19 Vaccine Antigen Is ANTHRAX Dr. Ariyana Love By Dr. Ariyana Love Covid-19 vaccines use self-replicating, programmable nanotechnology and synthetic, modified RNA (modRNA) otherwise known as Spike Protein. We are told that a vaccine antigen is used in the Covid-19 technology to “evoke an immune response” but what if the Covid-19 vaccine antigen is ANTHRAX? “…hardly any natural pathogens are really well suited to being biowarfare agents from a military point of view. Such a bioweapon must fulfill a variety of demands: it needs to be produced in large amounts, it must act fast, it must be environmentally robust, and the disease must be treatable… only a minority of natural pathogens are suitable for military purposes. “Anthrax is of course the first choice because the causative agent, B. anthracis, fulfills nearly all of these specifications.” Anthrax was developed by Russia in 1950. According to the NIH, the USSR’s ‘invisible anthrax’ was created by introducing an “alien gene” into the highly deadly Bacillus Anthracis bacteria. This means that Cross-Species-Genomics capability was acquired by governments before 1950. A lethal bacterium and an alien gene were genetically altered and blended together to produce the deadly bioweapon known as Anthrax. Russia’s Anthrax could be treated with antibiotics even several days after exposure, and thus it met the requirements under the Biological Weapons Convention. A bioweapon of choice, Anthony Fauci decided to increase Anthrax lethality and the NIH began genetic attenuation before 2006. Through GAIN-and-LOSS-of-Function the NIH produced a more drastic and deadly Anthrax that’s resistant to antibiotics and more. According to a University of Minnesota publication, the United States D.O.D smuggled shipments of live B anthracis spores from the Army’s Dugway Proving Ground in Utah, to other labs in the United States and abroad (Source: USA Today). The U.S. Army sent shipments of live samples of Anthrax to 86 labs outside the U.S. over a period of 10 years (Source: The Daily Beast). Transfers of samples of live B anthracis and the H5N1 influenza bioweapon were sent from CDC labs to other labs. CDC correspondence released under the Freedom of Information Act shows that labs studying bioterror pathogens “have failed over and over to comply with important safety and security regulations.” The D.O.D. tried to cover for the CDC, claiming “system failure” was to blame for the lab leaks, but we already know that the D.O.D spearheaded this “Covid-19 vaccine” roll-out. Please see: Aerosolized inoculation of Anthrax – Aerosolized Intratracheal Inoculation of Recombinant Protective Antigen (rPA) Vaccine Provides In 2007, Anthony Fauci created the H7N9 bioweapon, otherwise known as the “influenza vaccine.” The NIH, CCP and the Israeli state collaborated through GAIN-and-LOSS-of-Function to produce the H7N9 “flu vaccine” and the new and improved “Aerosolized Anthrax Vaccine”. Ofir Israeli from the Israel Institute of Biological Research, sequenced the Bacillus anthracis V770-NP1-R Strain in 2014, creating a synthetic chemical bioweapon. The Israeli state oversaw the animal trials for the Anthrax “vaccine” and told us it was safe and effective. Meanwhile, the Israeli company called Sanofi Pasteur developed the first H7N9 “vaccine” and trialed it for the NIH in 2014. Also in 2014, the NIH developed the H7N9 “influenza vaccine” to be droplet transmissible. Simultaneously, in 2014 China achieved a 99% transmissibility of the H7N9 “flu vaccine”. China also trialed the first aerosolized intratracheal Anthrax “vaccine” on mice. The study revealed severe side effects. PLEASE SEE: NIH Using DEAD CORPSES To Make “Virus”; Gain Of Function Weaponized Dead Corpses The Israeli state, NIH and China turned their new and improved Anthrax bioweapon into an attenuated antigen to be used in vaccines under the guise of “evoking an immune response” and “vaccine immunity.” The nations have been intentionally poisoned with biowarfare. In March 2022, the Russian military discovered that the Covid-19 bioweapons are being developed in U.S. biolabs in Ukraine. This includes the plague, Ebola, Filoviruses’, Anthrax and more. Anthrax causes hemorrhaging. So does Ebola and Marburg. Ebola is used in the J&J and Sinovax jabs, while Filovirus is used in Moderna. Ebola and Marburg are both Anthrax. H7N9 is used in all “flu vaccines” while Anthrax is being used as a “vaccine adjuvant” in all Covid-19 jabs and swabs. Through Loss-Of-Function, genetic deletions were performed inside the B. anthracis bacteria to improve replication of the bacteria in vivo. This ensured hospital protocols would not work to stop the Anthrax from replicating inside the human body after inoculation due to it being antibiotic resistant. The B. anthracis bacteria was also genetically modified to survive in insect hosts so as not to sporulate before it’s injected into the human host by a Bill Gates GMO mosquito which is part of DARPA’s weaponized insect project called The Sentinels. Incidentally, the CDC owns the Anthrax isolate patent that was funded by the U.S. Government. This is treason. The CDC also says that a bioterrorist attack would most likely be Anthrax. Please see: Malaria Parasites In “Vaccines” Target Placenta, Kill Babies In Utero SPIKE PROTEIN IS AEROSOLIZED ANTHRAX There are 232 B. anthracis genomes that are currently available in the GenBank database. There’s an Anthrax “vaccine” for cattle and two strains are licensed for use in humans. There exist two patents for an “Aerosolized Anthrax Vaccine.” The first Anthrax “vaccine” patent for humans is partly owned by the U.S. Government. The second is a “Recombinant Anthrax Vaccine”. “The spores of the toxigenic, nonencapsulated B. anthracis STI-1 strain and the cell-free PA-based “vaccines” consisting of aluminum hydroxide-adsorbed supernatant material from cultures of the toxigenic, nonencapsulated B. anthracis strain V770-NPI-R or alum-precipitated culture filtrate from the Sterne strain. Each of these Anthrax toxins are being used for “cellular entry in humans“. The LF is a metalloprotease recently shown to cleave the amino termini of the mitogen-activated protein kinase kinases 1 and 2, which results in their inactivation.” The above quote from the Recombinant Anthrax Vaccine patent reveals that the poisonous Anthrax “antigen” is being used to genetically modify the genome of humans (cellular entry into humans). By cleaving to the amino termini, protein kinases 1 and 2 are inactivated. This is accomplished by genetic deletions. The molecular basis of Anthrax “vaccines” includes “spores and DNA plasmids” that are entering human cells. The following quote about the Anthrax “protective antigen” is particularly revealing: “PA (protective antigen) is the common receptor binding domain of the toxins and can interact with the two different effector domains, EF and LF, to mediate their entry into target cells (14).” Anthrax is being used to “regulate gene expression by binding to DNA sequences and modulating transcriptional activity through their effector domains”. Pharma has essentially found a way to encode any synthetic proteins into the human genome from any species they want, including bacteria. The “Aerosolized Anthrax Antigen” is being encoded into target cells to make those cells produce the chemical drug called Anthrax. This is how the Anthrax “vaccine” is aerosolized. Once a person is inoculated with the Covid-19 bioweapon through subcutaneous injection or nasopharyngeal delivery with contaminated PCR swabs, the weapon system will begin genetic deletions and encoding the genome of target cells with the Anthrax spike protein. A person begins producing the toxic spike protein and shedding Anthrax into the air, exposing everyone to Inhalation Anthrax. It’s a weapon system that is intentionally aerosolized. This study admits that the Anthrax spores from B. anthracis STI-1 strain and B. anthracis strain V770-NPI-R used in the “aerosolized Anthrax vaccines” are toxigenic. The Sterne strain which is used to inoculate our food supply (animals) is also genotoxic. This NIH study explains how a “replicon” of the Bacillus anthracis bacteria was cloned into an Escherichia coli (E. coli) “vector” using cross-species-genomics. These two bacteria were synthetically fused together to enhance lethality. ALHYDROGEL According to the “aerosolized Anthrax vaccine” patents, the so-called “vaccine adjuvant” used is a DARPA weapon system called Alhydrogel. Hydrogel technology was developed over many years during a collaboration between DARPA and Profusa, a private biotech company specializing in the development of tissue-integrated biosensors. In 2018, DARPA published a video revealing their intention to use this biosensing technology for both military and public health. In the Alhydrogel invention, Anthrax was fused together into a nanogel called Alhydrogel, consisting of fibrous nanoparticles (Nanofibers) that are “antigen specific to CD4+ T cells”. In layman’s terms, the nanorobots are intentionally programmed to target and alter the genome of CD4-T cells, inducing cell death. This essential part of our immune system (T-cells) stop foreign invaders from entering our cells. Destroying our T-cells enables the government’s operating system to take root in the body and quicken death. Alhydrogel is infused with 750 μg of aluminum, making it magnetic. Nanofibers are used for self-assembly and electrospinning, for tissue engineering and delivery of drugs and chemicals into the brain. Being magnetic and nanotech based, the Alhydrogel can replicate everywhere in the body and wire a new neural network. Astonishingly, Alhydrogel is already the most widely used vaccine adjuvant! There are many Alhydrogel patents that contain toxic cocktails that will overwhelm anyone’s immune system. This Alhydrogel patent demonstrates it’s use of the B anthracis bacteria, E. coli, N. gonorrhoeae, Chlamydia, Staphylococcus, TB and more. It also contains the H5N1 influenza bioweapon, RNA, DNA synthesis and Polysorbate 80 for Blood Brain Barrier (BBB) permeability. This begs the question, where do venereal diseases come from? This Nature article reveals that 2% Alhydrogel is used in all Covid-19 “vaccines”. Previously, aluminum salts were the only adjuvants licensed for vaccine use in humans in the U.S. In recent decades, nanoparticle adjuvants in hydrated gels were introduced. The article continues by saying that the “influenza vaccine” was the first to use Alhydrogel. “Aluminum salt-based adjuvants such as alhydrogel have been a mainstay of vaccines for decades” boasts Christopher B. Fox and colleagues at the Infectious Disease Research Institute in Seattle, USA. Both nanoparticles and Anthrax have been used in vaccines for decades already, without the Informed Consent of the public. Alhydrogel was improved and transformed into the Nanoalum adjuvant. Here, we introduce a top-down manufacturing process—high-pressure microfluidization—to generate aluminum oxyhydroxide nanoparticles, hereupon referred to as nanoalum, using the clinically approved Alhydrogel adjuvant as the precursor. Alhydrogel is also carried in the lipid coating of nanoparticles. The “Aerosolized Anthrax Vaccines” also contain SEQ ID NO: 1 which is owned by the Pirbright Institute (Bill & Melinda Gates). SEQ ID NO: 1 contains the world’s most deadly genetically modified parasites. Please see: MEGA BOMBS! GMO Parasites Are The mRNA Vector! ANTHRAX SYMPTOMS AND TREATMENT Anthrax has been deployed on the population by three methods; injection, inhalation and skin penetration. The mortality rate for Anthrax varies depending on the method of exposure. It’s approximately 20% fatality for cutaneous Anthrax and 25–75% for Gastrointestinal Anthrax. Inhalation Anthrax is by far the worst with a fatality rate that is 80% or higher. Inhalation Anthrax is what we’re all being exposed to from the Covid-19 jabs and contaminated PCR swabs. Antibiotics constitute the mainstay of treatment against Anthrax, despite the fact that they won’t work to stop its replication due to the NIH, China and Israel’s GAIN-and-LOSS-of-Function enhancements (antibiotic resistance). Pharmaceutical experimental genotoxic drugs such as Oblitoxaximab and Raxibacumab are being touted as Anthrax treatments but these are monoclonal antibodies. We know from the monoclonal antibody patents that they’re also the “mRNA vaccine” weapon system. Anytime you inject recombinant proteins or modRNA into humans, it’s extremely toxic and will be rejected by our immune system 100% of the time. Please read: Monoclonal Antibodies Is mRNA Gene Knockdown Tech, Encoding HIV – Patent Review Pharma wants us to believe that the only known effective “prevention” against Anthrax is the Anthrax “vaccine”. However, the Anthrax “vaccine” inoculation given to U.S. military troops was a horrific disaster. U.S. Army statistics that were never published, show the Anthrax “vaccine” induces turbo cancers. The toxicological harms of Anthrax are many. It causes severe heart issues. Could this be a contributing factor to Myocarditis and Pericarditis? Anthrax also coagulates the blood. “Pathophysiological changes associated with anthrax lethal toxin included loss of plasma proteins, decreased platelet count, slower clotting times, fibrin deposits in tissue sections, and gross and histopathological evidence of hemorrhage. These findings suggest that blood vessel leakage and hemorrhage lead to disseminating intravascular coagulation and/or circulatory shock as an underlying pathophysiological mechanism.” Read more here and here. Anthrax induces hemorrhaging. So this explains all the excessive bleeding people have experienced over the last 4 years, following Covid-19 inoculation and from aerosolized exposure, otherwise known as the “shedding” phenomenon. This is a result of Inhalation Anthrax. It becomes clear that the newly dubbed “White Lung Syndrome” and the Chinese ‘pneumonia’ outbreak is none other than Inhalation Anthrax. Mycoplasma pneumonia is on the rise, and it’s listed on Pfizer’s internal documentation as a known Adverse Effect of the Covid-19 inoculation. This study reveals that Mycoplasma Pneumonia is aerosolized. WHO also confirms this phenomenon is Mycoplasma Pneumonia. All naturally occurring bacterium have cell walls. Mycoplasmas are spherical to filamentous cells with no cell walls. It’s genetically manipulated in a laboratory by GAIN-of-Function for the purpose of enhancing replication inside the human body, making it more lethal. Mice “treated” with anthrax lethal toxin (LT) exhibit hemorrhage and liver damage. Monocyte procoagulant responses to anthrax peptidoglycan are reinforced by proinflammatory cytokine signaling and histological lesions in the spleen. Anthrax has already been tested on the public. According to the NIH, Anthrax spores were intentionally released into “some environments” in NYC during 9/11. According to the NIH, the FBI launched an investigation called “Amerithrax”. It was “one of the largest and most complex (investigation) in the history of law enforcement”, according to the FBI. Heroine users in Europe have been tested with Injection Anthrax. Our skies are sprayed with smart dust and chemicals daily. Our governments have launched an all-out war against their constituents. We are being poisoned in a myriad of ways, so please keep this in mind: “Anthrax is easy to produce in large quantities, highly lethal, relatively easy to develop as a weapon, easily spread over a large area, easily stored and dangerous for a long time. Given appropriate weather and wind conditions, 50 kilograms of aerosolised anthrax spores released from an aircraft along a 2 kilometer line could create a lethal cloud of anthrax spores that would extend beyond 20 kilometers downwind. The aerosol cloud would be colorless, odorless and invisible following its release. Given the small size of the spores, people indoors would receive the same amount of exposure as on the street. There are currently no atmospheric warning systems to detect an aerosol cloud of anthrax spores. The first sign of a bioterrorist attack would most likely be patients presenting with symptoms of inhalation anthrax. A 1970 analysis by World Health Organization concluded that the release of aerosolized anthrax upwind to a population of 5,000,000 could lead to an estimated 250,000 casualties, of whom as many as 100,000 could be expected to die. A later analysis, by the Office of Technology Assessment of the U.S. Congress estimated that 130,000 to 3 million deaths could occur following the release of 100 kilograms of aerosolized anthrax over Washington D.C., making such an attack as lethal as a hydrogen bomb.” TREATMENT If you have been inoculated with Covid-19 or PCR swabbed, and you are suffering from heart pain, unusual bleeding, skin rashes and abrasions, it could be Injection Anthrax. If you are “unvaccinated” and hemorrhaging from being around “vaccinated”, then you may have been exposed to Inhalation Anthrax. Many doctors, including myself, have documented persistent bleeding rectally, violent bleeding vaginally, nasally and in the eyes. Since October 4th, I have received many reports of a red eye syndrome where the entire eye is blood-red. This makes sense because eye tissue is more sensitive. If you have been exposed to Inhalation Anthrax, you may feel hot and severely flushed, and you may break out in big, red splotches on your skin, followed by a completely red eye in the morning. Although they don’t get much attention, “anti-toxins have long been considered an essential ‘adjunctive’ therapy, and remain so”, according to the NIH. Anti-toxins are the natural medicines that detox poisons. In other words, you need an effective natural medicine detox protocol. I have been successfully detoxing people from the Covid-19 bioweapons for three years. Since I began treating people presenting with Anthrax poisoning with strong antibacterials, my clients are experiencing quicker detox results. If you would like to schedule a consultation with me, please do so through my online booking system. Please follow me on Telegram @drloveariyana and X @drloveariyana. If you would like to donate to my research, please do so here. UPDATE: My Anthrax article is now fully edited and published on Substack. Please review and SHARE. The Covid-19 Vaccine Antigen Is ANTHRAX Read more: https://open.substack.com/pub/drloveariyana/p/the-covid-19-vaccine-antigen-is-anthrax?r=2juwfo&utm_campaign=post&utm_medium=web&showWelcomeOnShare=true https://donshafi911.blogspot.com/2024/02/the-covid-19-vaccine-antigen-is-anthrax.html
    Angry
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  • What If Everything They’ve Been Telling You About Food Is… WRONG?
    Vigilant NewsFebruary 2, 2024
    By Brian Cates

    The last 9 months have been an exceedingly strange journey for me.

    While I had already figured out the FDA food pyramid was garbage and had watched in real-time as all the federal “medical” “health” “science” agencies played a direct role in suppressing accurate information on COVID-19 and C-19 origins, treatments, vaccines, etc., it took me the better of part of 3 years to begin critically and logically examining what these self-same propagandists disguised as ‘experts’ have been telling all of us about food and what supposedly comprises a healthy diet.


    I’d struggled with my weight since I was a young man of 24. I am soon turning 60.

    I’d spent the past few years talking about losing weight and the all the issues I was dealing with from lugging around over 100+ pounds of useless bodyfat.

    But I was still eating 4-5 times a day, at least two of those meals being sizable. And though I cut down on the sweets and was eating what I was told were ‘healthy whole grains’, the weight not only refused to go down, it kept going up.

    I would go through the same cycle several times from when I was around 26 to last year: Start working out religiously, while eating what I was told was mostly ‘healthy’ food. I’d add some muscle, my weight would drop maybe 20 pounds or so…and then after 3-4 months, hit the wall. No changes, and despite working out, the weight crept back up. Quit working out, gain all the weight back, a year goes by…then start the cycle again.

    34 years or so I ran on this hamster wheel.

    When this picture was taken, I’d just started writing for The Epoch Times in mid-2018. I was 350 pounds or so. Hadn’t weighed myself in a while. I was too scared to look anyway.

    Image
    I had just gone through the cycle again early last year.

    Working out, eating the “healthy food” chock full of carbs, various forms of sugars and toxic seed oils & chemicals, etc., etc. Then in May, I quit again.

    In late June, my stepmom visited me in my new house in Florida while I was on an RV tour around the US, and when she saw how I was living and eating, she read me the riot act. She kicked me in the ass and got me not only moving again, but that visit was also the catalyst I needed to go back and re-examine 35+ years of failure and why trying the same thing over and over again wasn’t working.

    For years, people like me were told this was a willpower/laziness thing. You’re fat and you can’t lose the weight because you don’t eat right/work out hard enough or long enough, etc.

    So I was mentally beaten down after exhausting myself on this hamster’s wheel as I was headed into decade #4 with the wrong programming in my head.

    Overweight Man Tired after Training, with Hand on Forehead Against ...
    But here’s the thing.

    As a journalist, I’d just spent the last 3 1/2 years extensively and exhaustively covering how federal and state and county ‘health’ ‘medical’ and ‘science’ ‘experts’ had just engaged in a deliberate conspiracy to hide and censor true and accurate information from the American public.

    Not to mention also covering the amount of gaslighting we were all being hit with following the blatant theft of the 2020 election from Donald Trump.

    So at this time, in late June/early July of last year, I started my re-examination of around 35 years of failure with an intriguing thought:

    **COULD IT BE** that the very same ‘health’ ‘medical’ & ‘science’ experts who’d just exposed and outed themselves as Big Pharma propagandists and business partners lying to us about COVID & many of the drugs involved in the treatment/prevention of infection…were also wrong or deliberately misleading us about….food?

    Image
    Could it possibly be….
    One of the first things I realized, when I began examining what the federal ‘health’ ‘medical’ ‘science’ agencies tout as a ‘healthy’ diet, is that when they last changed the food pyramid in the early 1990’s, the rates of both obesity and diabetes exploded in this country as people began following this ‘expert’ advice.

    As you can see from the graphs below, an already alarming rising trend suddenly shot dramatically upward in the early 1990s.

    Image
    Image
    How bad has the obesity/diabetes/insulin resistance crisis gotten in the US?

    It is now so bad they’ve coined a bullshit term – ‘prediabetes’ – to try to mask the deadly seriousness of the crisis. If you are diagnosed as ‘prediabetic,’ you ARE diabetic; it’s just that your insulin resistance hasn’t progressed to such an extent that they’ll officially call it ‘diabetes.’

    Image
    Or as actor Wilford Brimley would say:

    Wilford Brimley Has Diabeetus - Misc - quickmeme
    Insulin resistance leads directly to a massive amount of chronic health issues of which diabetes is only one.


    By giving Americans the ‘expert’ advice that they needed to start chugging down ‘6-11 servings’ every day of ‘healthy whole grains’ and cook their food with seed oils while counseling them to also **reduce** the amount of meat and animal fats they were eating, Americans began ingesting way more carbohydrates and PUFA’s [that’s ‘polyunsaturated fatty acids, for those of you in Rio Linda…] every day than they’d been eating before.


    And yet I recall for the past 30 years or so watching the popular culture health reporters scratch their heads and wondering what could possibly be causing the massive explosion of obesity and chronic illnesses, as well as the dropping testosterone and estrogen levels they were observing.


    So the fact that the federal ‘health’ agencies caused much of the country to make a dramatic wrong turn that exacerbated the rising trends of obesity and chronic illness with their drastically wrong official ‘food pyramid’ in the early 1990s, caused me to wonder:

    If they were giving the American public such rotten, terrible, horrible, no-good ‘expert’ instructions on what they should be eating every day, **what else** have they been telling us that is utter bullshit?

    And the very first thing I stumbled over in this regard was the history of SEED OILS and how medical scientists doing animal experiments back in the 1890s/early 1900s quickly established that seed oils were toxic and harmful to growing and developing animals.

    By the end of July last year, I was sharing the alarming stuff I was finding in my research with my readers on my Substack:

    Image
    You have to fully grasp this. They **knew** from animal experiments on rats and cows and horses and birds **exactly** what SEED OILS did to growing and developing animals.

    Many of these experiments were carried out from the late 1880s through the 1910s. Experiment results were published in books, such as this one from scientist E.V. McCollum in 1918.



    There was no mystery here. The results were established and easily observable.

    And yet…what ended up happening over the next 100 years?

    Government ‘health’ experts working hand-in-glove with Big Food corporations convinced most Americans to stop cooking their food with butter, lard, and tallow, and instead use the new ‘Crisco’ and other highly processed seed oils and margarine. Because they claimed these new processed products were ‘healthier’.

    And because Americans back then were very trusting people who didn’t know their government was controlled by hidden corporations and interests out to make massive profits while not caring about their health, they followed this ‘expert’ advice from authority figures they were taught to trust.

    From the 1920s through today, Big Food, working in conjunction with Big Government, began creating many new highly processed foods that contained large amounts of these seed oils and myriad toxic chemicals and food additives. Our American culture is now flooded with highly processed fake ‘food’ that didn’t exist even 100 years ago. And they are inventing new kinds of fake food every year.

    Image
    If they knew what seed oils would do to human beings who began eating them early in life, and ate them throughout their physical development and into adulthood – and evidence seems to suggest they did – then the only possible reason for them to do that would be to arrest the development of children, cause chronic illnesses throughout life, and ensure a premature death.

    What I saw through my research was **deeply disturbing to me**.

    Image
    This can’t be just about profit motive, the fact they’d make a lot of MONEY creating new addictive processed sugar-and-carb-and-seed oil-filled foods. They had to also have seen the very real and OBVIOUS HARM they would be doing to their fellow citizens by introducing these heavily toxic and health-destroy products into the American food supply.

    Not when you realize the wealthy elite who run everything in this fallen world behind the scenes are constantly wringing their hands and brainstorming about how to ‘fix’ the world’s overpopulation problem, think even the concept of human rights is a big funny hilarious joke, and that human rights don’t exist, just like God doesn’t exist.

    They’ve always sat around at their big, important conferences in places like Davos and talked about culling the human herd like they’re ranchers planning for the next cattle drive. It’s just that they’re starting to get embarrassed that the cows are now spying on them in the barn and figuring out what they’re talking about, their plans for the rest of us.

    What more clever way could be devised than convincing people to simply EAT themselves into chronic illnesses that will guide them expeditiously into an early grave?

    The rise in life expectancy rates over the past 100 years is not because people are HEALTHIER overall.

    Image
    Far from it.

    The rates rose because of medical advancements in keeping chronically ill people alive longer.

    Were people not being tricked and misled into fattening themselves with constant insulin resistance and filling their bodies with toxins, most people would very likely be living into their upper 90s by now. Instead, life expectancy is dropping because the amount of toxic and unhealthy food Americans are eating is going up.

    This cannot be overstated. With the medical/health/scientific advancements in knowledge and technology over the past 120 years, the only way this was allowed to happen and to become so widespread at this point millions of people are dying from easily preventable chronic illnesses is that…

    …and I know some of you will struggle to accept this….

    …the real owners of the world out there **wanted** this to happen. They demanded it.

    There’s no way they don’t know. So if they know…and nothing’s been done to stop it? It’s not just about money. There’s what looks like an exceedingly nefarious agenda at work here.

    Image
    Sometimes in my more paranoid moments, I wonder if….

    Nah. Couldn’t be….

    Could it?

    Image
    Tastes like chicken!
    https://www.youtube-nocookie.com/embed/W-JhfjGtlp8?rel=0&autoplay=0&showinfo=0&enablejsapi=0
    So the first two things I discovered in my new research starting in the middle of last year:

    1. The food pyramid was a massive ‘mistake’…or was it?

    2. Seed Oils are toxic and harm human development and shorten the human lifespan Yet they were allowed to proliferate into the American food supply by accident…or was it really an ‘accident’?

    Next, I discovered that the conventional ‘expert’ findings about animal fat were wrong.

    For decades I’d been endlessly told and had read that too much dietary animal fat caused health/heart issues. Cut down dramatically on the red meat, the eggs, the butter, replace the fat with ‘healthy’ food…

    And yet what do you actually **FIND** when you examine the medical research?

    You find when people dramatically reduced their animal fat intake they still got FATTER and more CHRONICALLY ILL. After all, one of the biggest reasons for creating a ‘new and improved!’ food pyramid back in the early 1990s was to convince people to CUT the amount of meat and animal fat they were eating and replace them with ‘healthy’ carbs.

    For people who were supposedly becoming more ‘healthy’ by following the new food pyramid’s ‘expert’ advice, Americans seemed to be getting fatter, heavier, and more unhealthy.

    It’s been noticed for some time now that people in America in the 1940s and 1950s sure do look pretty darn healthy, even though we were constantly being told by our modern ‘health experts’ that those poor folks were eating WAY too much animal fats and red meat and eggs and [gasp!] butter.

    I mean…there’s just NO WAY that Americans back then eating all that bad stuff were healthier than US today, right?



    Why, that very idea would be absurd! They didn’t know any better! They didn’t have our advantages!

    Image
    Image
    Image
    Hey…maybe it’s time for us to stop, go back and look, and rethink this all out again…

    Because SOMETHING clearly isn’t working.

    We’re **supposed to be** far healthier than those poor fools back in the 1940s and 1950s…but we’re NOT.

    Why is that?

    If you commit yourself to finding the truth and facing it unflinchingly, no matter where it leads…you can find it.

    The brutal truth is…people here in America have been misled. Just about EVERYTHING the ‘health’ and ‘diet’ ‘experts’ have been telling them all their lives is….SURPRISE!…wrong.

    It’s not your fault. It is THEIR fault. They either didn’t know what they were talking about when they were teaching you how to eat, or they had a hidden agenda.

    Either way…NOT YOUR FAULT.

    Image
    Image
    Image
    Its not that you lack willpower. Or that you’re lazy. Or that you don’t work out enough.

    Its that what the ‘experts’ taught you about how to eat a proper diet wasn’t true. You were not getting accurate information.

    You were steered towards unhealthy seed oil/sugar/carb-filled processed foods because authority figures you trusted gave you terrible advice.

    You were given bad information by government and medical authority figures on 7 dietary subjects:

    1. Cholesterol levels

    2. Salt/mineral levels

    3. Protein levels

    4. Animal Fats

    5. Fiber

    6. Seed oils

    7. Meal frequency

    My research has led me to conclude that we need to go BACK to how our ancestors ate. A mostly meat diet where we do not eat large meals of highly processed fake foods several times a day with snacks in between.

    We’re not designed to put food into our stomachs 3-6 times a day, constantly spiking our insulin levels and hormonal system, developing lifelong insulin resistance and metabolic syndrome-related chronic illnesses and diseases.

    Especially not the kind of food we’re surrounded by in our popular culture, the highly over-processed stuff that didn’t exist 100 years ago that are now chock-full of toxic seed oils, sugars, and chemicals.

    Sure, people back in the 1940s and 1950s were eating 3 squares a day, but look at **what** they were eating compared to what we are surrounded by now. Until around 120 years ago, most people lived on farms, and even if they didn’t, most of the food they ate came almost directly from a farm.

    Have you heard stories about people who travel to Europe and visit places like France and Italy where they eat all the bread and pasta, drink all the wine they want, etc. and don’t get fat? Know why that is?

    Because it’s ILLEGAL over there in many European countries to add in the toxic chemical crap they put into US processed food on this side of the pond. Look at the following links for just a HINT of how bad this issue is. Why are European governments taking better care of their people’s health than our supposedly superior US government?

    https://www.cbsnews.com/news/us-food-additives-banned-europe-making-americans-sick-expert-says/
    https://www.theguardian.com/us-news/2019/may/28/bread-additives-chemicals-us-toxic-america
    https://foodrevolution.org/blog/banned-ingredients-in-other-countries/
    https://www.theguardian.com/environment/2022/jun/23/titanium-dioxide-banned-chemicals-carcinogen-eu-us
    Image
    So, when I began changing my diet again in 2023, I switched to a [O]ne [M]eal [A] [D]ay program [OMAD] where I ate only once time in every 24-hour period.

    I adopted a 4-hour ‘feeding window’ from 4 pm to 8 pm.

    I also cut out most of the processed foods I had been eating – including the Weight Watcher’s stuff. I increased the amount of meat I ate from around 1/3rd of my diet to 2/3rds.

    From late June through early September, I went from 345 pounds [my stepmom made me get on the scale with her watching. I expected to see around 320. Ulp!] down to 320.

    And then I got stuck. The weight stopped coming off and I fluctuated between 317 and 320 for around a month and a half.


    Then my ‘little sister from another Mister,’ investigative journalist and head editor of Uncover DC, Tracy Beanz, shared some pictures and testimony about her husband William, who had lost over 160 pounds on a Carnivore Diet in one year. He not only lost a massive amount of unhealthy body fat, but he also had several chronic health issues evaporate.

    Image
    Image
    So….in early November, I decided to cut out the bread and the potatoes and the ‘healthy’ cereal I was still eating and stay only with raw milk and unpasteurized cheese for my carbs, and the rest of my diet was Amish-farm raised beef, bison, chicken, turkey, and fish with large brown eggs.

    The weight started coming again…slowly. I went from 320 down to my current weight of 295. I’ve gone down to 293, but 295 is what I saw the last 2 times I weighed myself.

    So. I learned a lot in the last 8 months. I wanted to share some of what I learned in this thread.

    I am not telling or advising anyone to do what I’m doing. I’m providing information and asking for people to check this out for themselves and make up their own minds.

    A key part of The Great Awakening is, I am convinced, teaching people how to get healthy and stay that way. And if people have been getting wrong and perhaps even deliberate disinformation from ‘health experts,’ the more people realize that and start reassessing what they’ve been told over the past few decades?

    THAT’S A BEAUTIFUL THING.



    https://vigilantnews.com/post/what-if-everything-theyve-been-telling-you-about-food-is-wrong/


    https://donshafi911.blogspot.com/2024/02/what-if-everything-theyve-been-telling.html
    What If Everything They’ve Been Telling You About Food Is… WRONG? Vigilant NewsFebruary 2, 2024 By Brian Cates The last 9 months have been an exceedingly strange journey for me. While I had already figured out the FDA food pyramid was garbage and had watched in real-time as all the federal “medical” “health” “science” agencies played a direct role in suppressing accurate information on COVID-19 and C-19 origins, treatments, vaccines, etc., it took me the better of part of 3 years to begin critically and logically examining what these self-same propagandists disguised as ‘experts’ have been telling all of us about food and what supposedly comprises a healthy diet. I’d struggled with my weight since I was a young man of 24. I am soon turning 60. I’d spent the past few years talking about losing weight and the all the issues I was dealing with from lugging around over 100+ pounds of useless bodyfat. But I was still eating 4-5 times a day, at least two of those meals being sizable. And though I cut down on the sweets and was eating what I was told were ‘healthy whole grains’, the weight not only refused to go down, it kept going up. I would go through the same cycle several times from when I was around 26 to last year: Start working out religiously, while eating what I was told was mostly ‘healthy’ food. I’d add some muscle, my weight would drop maybe 20 pounds or so…and then after 3-4 months, hit the wall. No changes, and despite working out, the weight crept back up. Quit working out, gain all the weight back, a year goes by…then start the cycle again. 34 years or so I ran on this hamster wheel. When this picture was taken, I’d just started writing for The Epoch Times in mid-2018. I was 350 pounds or so. Hadn’t weighed myself in a while. I was too scared to look anyway. Image I had just gone through the cycle again early last year. Working out, eating the “healthy food” chock full of carbs, various forms of sugars and toxic seed oils & chemicals, etc., etc. Then in May, I quit again. In late June, my stepmom visited me in my new house in Florida while I was on an RV tour around the US, and when she saw how I was living and eating, she read me the riot act. She kicked me in the ass and got me not only moving again, but that visit was also the catalyst I needed to go back and re-examine 35+ years of failure and why trying the same thing over and over again wasn’t working. For years, people like me were told this was a willpower/laziness thing. You’re fat and you can’t lose the weight because you don’t eat right/work out hard enough or long enough, etc. So I was mentally beaten down after exhausting myself on this hamster’s wheel as I was headed into decade #4 with the wrong programming in my head. Overweight Man Tired after Training, with Hand on Forehead Against ... But here’s the thing. As a journalist, I’d just spent the last 3 1/2 years extensively and exhaustively covering how federal and state and county ‘health’ ‘medical’ and ‘science’ ‘experts’ had just engaged in a deliberate conspiracy to hide and censor true and accurate information from the American public. Not to mention also covering the amount of gaslighting we were all being hit with following the blatant theft of the 2020 election from Donald Trump. So at this time, in late June/early July of last year, I started my re-examination of around 35 years of failure with an intriguing thought: **COULD IT BE** that the very same ‘health’ ‘medical’ & ‘science’ experts who’d just exposed and outed themselves as Big Pharma propagandists and business partners lying to us about COVID & many of the drugs involved in the treatment/prevention of infection…were also wrong or deliberately misleading us about….food? Image Could it possibly be…. One of the first things I realized, when I began examining what the federal ‘health’ ‘medical’ ‘science’ agencies tout as a ‘healthy’ diet, is that when they last changed the food pyramid in the early 1990’s, the rates of both obesity and diabetes exploded in this country as people began following this ‘expert’ advice. As you can see from the graphs below, an already alarming rising trend suddenly shot dramatically upward in the early 1990s. Image Image How bad has the obesity/diabetes/insulin resistance crisis gotten in the US? It is now so bad they’ve coined a bullshit term – ‘prediabetes’ – to try to mask the deadly seriousness of the crisis. If you are diagnosed as ‘prediabetic,’ you ARE diabetic; it’s just that your insulin resistance hasn’t progressed to such an extent that they’ll officially call it ‘diabetes.’ Image Or as actor Wilford Brimley would say: Wilford Brimley Has Diabeetus - Misc - quickmeme Insulin resistance leads directly to a massive amount of chronic health issues of which diabetes is only one. By giving Americans the ‘expert’ advice that they needed to start chugging down ‘6-11 servings’ every day of ‘healthy whole grains’ and cook their food with seed oils while counseling them to also **reduce** the amount of meat and animal fats they were eating, Americans began ingesting way more carbohydrates and PUFA’s [that’s ‘polyunsaturated fatty acids, for those of you in Rio Linda…] every day than they’d been eating before. And yet I recall for the past 30 years or so watching the popular culture health reporters scratch their heads and wondering what could possibly be causing the massive explosion of obesity and chronic illnesses, as well as the dropping testosterone and estrogen levels they were observing. So the fact that the federal ‘health’ agencies caused much of the country to make a dramatic wrong turn that exacerbated the rising trends of obesity and chronic illness with their drastically wrong official ‘food pyramid’ in the early 1990s, caused me to wonder: If they were giving the American public such rotten, terrible, horrible, no-good ‘expert’ instructions on what they should be eating every day, **what else** have they been telling us that is utter bullshit? And the very first thing I stumbled over in this regard was the history of SEED OILS and how medical scientists doing animal experiments back in the 1890s/early 1900s quickly established that seed oils were toxic and harmful to growing and developing animals. By the end of July last year, I was sharing the alarming stuff I was finding in my research with my readers on my Substack: Image You have to fully grasp this. They **knew** from animal experiments on rats and cows and horses and birds **exactly** what SEED OILS did to growing and developing animals. Many of these experiments were carried out from the late 1880s through the 1910s. Experiment results were published in books, such as this one from scientist E.V. McCollum in 1918. There was no mystery here. The results were established and easily observable. And yet…what ended up happening over the next 100 years? Government ‘health’ experts working hand-in-glove with Big Food corporations convinced most Americans to stop cooking their food with butter, lard, and tallow, and instead use the new ‘Crisco’ and other highly processed seed oils and margarine. Because they claimed these new processed products were ‘healthier’. And because Americans back then were very trusting people who didn’t know their government was controlled by hidden corporations and interests out to make massive profits while not caring about their health, they followed this ‘expert’ advice from authority figures they were taught to trust. From the 1920s through today, Big Food, working in conjunction with Big Government, began creating many new highly processed foods that contained large amounts of these seed oils and myriad toxic chemicals and food additives. Our American culture is now flooded with highly processed fake ‘food’ that didn’t exist even 100 years ago. And they are inventing new kinds of fake food every year. Image If they knew what seed oils would do to human beings who began eating them early in life, and ate them throughout their physical development and into adulthood – and evidence seems to suggest they did – then the only possible reason for them to do that would be to arrest the development of children, cause chronic illnesses throughout life, and ensure a premature death. What I saw through my research was **deeply disturbing to me**. Image This can’t be just about profit motive, the fact they’d make a lot of MONEY creating new addictive processed sugar-and-carb-and-seed oil-filled foods. They had to also have seen the very real and OBVIOUS HARM they would be doing to their fellow citizens by introducing these heavily toxic and health-destroy products into the American food supply. Not when you realize the wealthy elite who run everything in this fallen world behind the scenes are constantly wringing their hands and brainstorming about how to ‘fix’ the world’s overpopulation problem, think even the concept of human rights is a big funny hilarious joke, and that human rights don’t exist, just like God doesn’t exist. They’ve always sat around at their big, important conferences in places like Davos and talked about culling the human herd like they’re ranchers planning for the next cattle drive. It’s just that they’re starting to get embarrassed that the cows are now spying on them in the barn and figuring out what they’re talking about, their plans for the rest of us. What more clever way could be devised than convincing people to simply EAT themselves into chronic illnesses that will guide them expeditiously into an early grave? The rise in life expectancy rates over the past 100 years is not because people are HEALTHIER overall. Image Far from it. The rates rose because of medical advancements in keeping chronically ill people alive longer. Were people not being tricked and misled into fattening themselves with constant insulin resistance and filling their bodies with toxins, most people would very likely be living into their upper 90s by now. Instead, life expectancy is dropping because the amount of toxic and unhealthy food Americans are eating is going up. This cannot be overstated. With the medical/health/scientific advancements in knowledge and technology over the past 120 years, the only way this was allowed to happen and to become so widespread at this point millions of people are dying from easily preventable chronic illnesses is that… …and I know some of you will struggle to accept this…. …the real owners of the world out there **wanted** this to happen. They demanded it. There’s no way they don’t know. So if they know…and nothing’s been done to stop it? It’s not just about money. There’s what looks like an exceedingly nefarious agenda at work here. Image Sometimes in my more paranoid moments, I wonder if…. Nah. Couldn’t be…. Could it? Image Tastes like chicken! https://www.youtube-nocookie.com/embed/W-JhfjGtlp8?rel=0&autoplay=0&showinfo=0&enablejsapi=0 So the first two things I discovered in my new research starting in the middle of last year: 1. The food pyramid was a massive ‘mistake’…or was it? 2. Seed Oils are toxic and harm human development and shorten the human lifespan Yet they were allowed to proliferate into the American food supply by accident…or was it really an ‘accident’? Next, I discovered that the conventional ‘expert’ findings about animal fat were wrong. For decades I’d been endlessly told and had read that too much dietary animal fat caused health/heart issues. Cut down dramatically on the red meat, the eggs, the butter, replace the fat with ‘healthy’ food… And yet what do you actually **FIND** when you examine the medical research? You find when people dramatically reduced their animal fat intake they still got FATTER and more CHRONICALLY ILL. After all, one of the biggest reasons for creating a ‘new and improved!’ food pyramid back in the early 1990s was to convince people to CUT the amount of meat and animal fat they were eating and replace them with ‘healthy’ carbs. For people who were supposedly becoming more ‘healthy’ by following the new food pyramid’s ‘expert’ advice, Americans seemed to be getting fatter, heavier, and more unhealthy. It’s been noticed for some time now that people in America in the 1940s and 1950s sure do look pretty darn healthy, even though we were constantly being told by our modern ‘health experts’ that those poor folks were eating WAY too much animal fats and red meat and eggs and [gasp!] butter. I mean…there’s just NO WAY that Americans back then eating all that bad stuff were healthier than US today, right? 🤔 Why, that very idea would be absurd! They didn’t know any better! They didn’t have our advantages! Image Image Image Hey…maybe it’s time for us to stop, go back and look, and rethink this all out again… Because SOMETHING clearly isn’t working. We’re **supposed to be** far healthier than those poor fools back in the 1940s and 1950s…but we’re NOT. Why is that? If you commit yourself to finding the truth and facing it unflinchingly, no matter where it leads…you can find it. The brutal truth is…people here in America have been misled. Just about EVERYTHING the ‘health’ and ‘diet’ ‘experts’ have been telling them all their lives is….SURPRISE!…wrong. It’s not your fault. It is THEIR fault. They either didn’t know what they were talking about when they were teaching you how to eat, or they had a hidden agenda. Either way…NOT YOUR FAULT. Image Image Image Its not that you lack willpower. Or that you’re lazy. Or that you don’t work out enough. Its that what the ‘experts’ taught you about how to eat a proper diet wasn’t true. You were not getting accurate information. You were steered towards unhealthy seed oil/sugar/carb-filled processed foods because authority figures you trusted gave you terrible advice. You were given bad information by government and medical authority figures on 7 dietary subjects: 1. Cholesterol levels 2. Salt/mineral levels 3. Protein levels 4. Animal Fats 5. Fiber 6. Seed oils 7. Meal frequency My research has led me to conclude that we need to go BACK to how our ancestors ate. A mostly meat diet where we do not eat large meals of highly processed fake foods several times a day with snacks in between. We’re not designed to put food into our stomachs 3-6 times a day, constantly spiking our insulin levels and hormonal system, developing lifelong insulin resistance and metabolic syndrome-related chronic illnesses and diseases. Especially not the kind of food we’re surrounded by in our popular culture, the highly over-processed stuff that didn’t exist 100 years ago that are now chock-full of toxic seed oils, sugars, and chemicals. Sure, people back in the 1940s and 1950s were eating 3 squares a day, but look at **what** they were eating compared to what we are surrounded by now. Until around 120 years ago, most people lived on farms, and even if they didn’t, most of the food they ate came almost directly from a farm. Have you heard stories about people who travel to Europe and visit places like France and Italy where they eat all the bread and pasta, drink all the wine they want, etc. and don’t get fat? Know why that is? Because it’s ILLEGAL over there in many European countries to add in the toxic chemical crap they put into US processed food on this side of the pond. Look at the following links for just a HINT of how bad this issue is. Why are European governments taking better care of their people’s health than our supposedly superior US government? https://www.cbsnews.com/news/us-food-additives-banned-europe-making-americans-sick-expert-says/ https://www.theguardian.com/us-news/2019/may/28/bread-additives-chemicals-us-toxic-america https://foodrevolution.org/blog/banned-ingredients-in-other-countries/ https://www.theguardian.com/environment/2022/jun/23/titanium-dioxide-banned-chemicals-carcinogen-eu-us Image So, when I began changing my diet again in 2023, I switched to a [O]ne [M]eal [A] [D]ay program [OMAD] where I ate only once time in every 24-hour period. I adopted a 4-hour ‘feeding window’ from 4 pm to 8 pm. I also cut out most of the processed foods I had been eating – including the Weight Watcher’s stuff. I increased the amount of meat I ate from around 1/3rd of my diet to 2/3rds. From late June through early September, I went from 345 pounds [my stepmom made me get on the scale with her watching. I expected to see around 320. Ulp!] down to 320. And then I got stuck. The weight stopped coming off and I fluctuated between 317 and 320 for around a month and a half. Then my ‘little sister from another Mister,’ investigative journalist and head editor of Uncover DC, Tracy Beanz, shared some pictures and testimony about her husband William, who had lost over 160 pounds on a Carnivore Diet in one year. He not only lost a massive amount of unhealthy body fat, but he also had several chronic health issues evaporate. Image Image So….in early November, I decided to cut out the bread and the potatoes and the ‘healthy’ cereal I was still eating and stay only with raw milk and unpasteurized cheese for my carbs, and the rest of my diet was Amish-farm raised beef, bison, chicken, turkey, and fish with large brown eggs. The weight started coming again…slowly. I went from 320 down to my current weight of 295. I’ve gone down to 293, but 295 is what I saw the last 2 times I weighed myself. So. I learned a lot in the last 8 months. I wanted to share some of what I learned in this thread. I am not telling or advising anyone to do what I’m doing. I’m providing information and asking for people to check this out for themselves and make up their own minds. A key part of The Great Awakening is, I am convinced, teaching people how to get healthy and stay that way. And if people have been getting wrong and perhaps even deliberate disinformation from ‘health experts,’ the more people realize that and start reassessing what they’ve been told over the past few decades? THAT’S A BEAUTIFUL THING. https://vigilantnews.com/post/what-if-everything-theyve-been-telling-you-about-food-is-wrong/ https://donshafi911.blogspot.com/2024/02/what-if-everything-theyve-been-telling.html
    VIGILANTNEWS.COM
    What If Everything They’ve Been Telling You About Food Is… WRONG?
    Have our trusted health authority figures led us astray? And if so... what can we do about it?
    0 Comentários 0 Compartilhamentos 36640 Visualizações
  • Virology - The Damning Evidence
    The Stake In The Heart For This Pseudoscientific Profession

    dpl
    Introduction

    One never realize how big the task of writing on a subject is until you start. One thing you can be assured of is how much you learn by writing about your findings or thoughts. My stance on virology has been clarified in two previous posts as follows:

    The Gatekeepers Club.

    Virus Lie - The Result of 4 Years of Study.

    Another thing you quickly realize on this journey is how easy it is to censor someone, especially if you start hitting a nerve. I have documented some of it underneath the conclusion of the The Gatekeepers Club article. It is very important to make copies of your work, as shadow banning is one thing, but if these platforms decide to terminate your channel and all the work you have done is on it, you will obviously lose it all. We were in that same position about a year ago when Discord decided to terminate our channel. Twenty of the smartest people you would ever know had been working on it for close to two years, and it was gone overnight. Therefore, this post will serve as safekeeping for some of the best information that I have come across in the last few weeks proving that virology is pseudoscience.


    Update - 18 September 2023

    The order of the sections of this article has been rearranged to introduce the most important information first. As mentioned in my most recent article titled: Hacking at the Root of the Virus Issue it was explained that for the longest time I thought that failure to “isolate” viruses was the most important evidence to focus on. This is however not the case as explained in detail in the “Hacking at the Root of the Virus Issue” article.

    Transmission is the fundamental assumption on which virology rest. Without proof of transmission, nothing downstream matters. Even though understanding these downstream concepts will never be a waste of time one must consider that the normal man on the street will not be interested in complicated terminology and processes.

    It is of crucial importance for the no virus community to find easier ways to explain the fallacy that is virology. Seeing as no one need a laboratory to assess whether transmission is possible and because we can observe this phenomena ourselves (Inductive reasoning) this is the linchpin for virology. A twitter space where we discussed this can be viewed here (*Note: Jamie was cut off during his talk and his section was not included).

    As discussed during the twitter space, we have reviewed the available transmission studies and a summary of these studies can be seen below.

    Transmission / Infection

    One of the funniest things you will see while debating the trolls on Twitter is that they will provide studies conducted to prove the efficacy of vaccines. The people that undertake these studies assume that transmission or infection has already been proven, but nothing could be further from the truth. That is why it is important for us to list the peer-reviewed studies that disprove transmission or infection to further demonstrate that virology is a pseudoscience. The list of studies was compiled with the help of Jamie, georgie&donny, and Aldhissla (also see Aldhissla’s list on polio here).

    (*Please note that this section is open to comments at the moment and anyone that want to add notes or studies are free to leave a comment).

    The Journal of Infectious Diseases, Vol. 2, No. 2 (Mar. 1, 1905):
    - Chapman, 1801: Tried to transmit measles using the blood, tears, the mucus of the nostrils and bronchia, and the eruptive matter in the cuticle without any success.
    - Willan, 1809: Inoculated three children with vesicle fluids of measles but without success.
    - Albers, 1834: Attempted to infect four children with measles without success. He quoted Alexander Monro, Bourgois, and Spray as also having made unsuccessful inoculations with saliva, tears, and cutaneous scales.
    - Themmen, 1817: Tried to infect 5 children with measles. 0/5 children became sick.

    Charles Creighton, 1837 (A history of epidemics in Britain). "No proof of the existence of any contagious principles by which it was propagated from one individual to another."

    EH Ackernecht, writing about Anticontagionism between 1821 and 1867 - “That the anticontagionists were usually honest men and in deadly earnest is shown, among other things, by the numerous self-experiments to which they submitted themselves to prove their contentions.” also see “Famous are the plague self-experiments of Clot-Bey, the offers for plague self-experiment by Chervin, Lassis, Costa, Lapis, and Lasserre, and the cholera self-experiments of Fay, Scipio Pinel, Wayrot, and J.L. Guyon. The amazing thing is that almost all of these experiments failed to produce the disease.”

    Note on Hospitals by Florence Nightingale, 1858 - "Suffice it to say, that in the ordinary sense of the word, there is no proof, such as would be admitted in any scientific inquiry, that there is any such thing as 'contagion." also see "Just as there is no such thing as 'contagion,' there is no such thing as inevitable 'infection."

    Andreas Christian Bull, 1868 - “It does not seem apparent in this small [polio] epidemic that contagion played any role, because the disease occurred here and there in the different places of the district without the possibility of establishing any relation between the various cases or the families of the same.”

    Karl-Oskar Medin, 1887 - A Swedish pediatrician who was the first to examine a polio outbreak, concluded that it was an infectious, but not contagious, disease.

    Charles Caverly, 1894 - Investigated the first US polio epidemic: ”it is very certain that it was non-contagious.”

    Journal of American Medical Association, Volume 72, Number 3, 1919 (or additional link here):

    - Warschawsky, 1895 - Injected small pigs and rabbits with blood taken in the eruptive stage. All results were negative.
    - Belila, 1896 - Placed warm nasal mucus and saliva from measles patients on the nasal and oral mucous membrane of rabbits, guinea-pigs, cats, mice, dogs and lambs, but without any positive results.
    - Josias, 1898 - Rubbed measles secretions over the throat, nose and eyes of several young pigs, but without any effects.
    - Geissler, 1903 - Inoculated sheep, swine, goats, dogs and cats in various ways with the bodily fluids from patients with measles; including smearing, spraying, rubbing. All results were negative.
    - Pomjalowsky, 1914 - Injected measles blood into guineapigs, rabbits and small pigs. All results were negative.
    - Jurgelunas, 1914 - Inoculated blood from patients with measles into suckling pigs and rabbits, but without effect.

    Leegaard, 1899 - Was not able to prove a single case of patient-to-patient contagion in a polio outbreak in Norway. "Infantile paralysis is of an infectious, but not of a contagious nature. As a matter of fact no indisputable instance of contagion could be proved."

    Dr. Rodermund, 1901 - From his diary of SmallPox experiments. For 15 years he smeared the pus of smallpox patients on his face and used to go home with his family, play cards at the gentleman’s club and treat other patients and never got sick or saw a single other person get sick.

    Walter Reed, 1902 - “Without entering into details, I may say that, in the first place, the Commission saw, with some surprise, what had so often been noted in the literature, that patients in all stages of yellow fever could be cared for by non-immune nurses without danger of contracting the disease. The non-contagious character of yellow fever was, therefore, hardly to be questioned.”

    Landsteiner & Popper, 1909 - "Attempts to transmit the disease [polio] to the usual laboratory animals, such as rabbits, guinea pigs, or mice, failed."

    F.E. Batten, (1909) - “Against the infectivity of the disease may be urged, first, the absence of spread of infection in hospital. The cases of poliomyelitis admitted to hospital freely mixed with other cases in the ward without any isolation or disinfection, some 70 children came in contact, but no infection took place. (p. 208, last paragraph)”

    The Boston medical and surgical journal, 1909 - An inquiry a 1908 polio outbreak found the following: “A large number of children were in intimate contact with those that were sick, and of these children an insignificant minority developed the disease.” 244 children were in intimate contact with those who were afflicted with polio. Of those 244 children, an "insignificant minority" developed the disease.

    Massachusetts State board of health, 1909 - "Poliomyelitis prevailed in epidemic form in Kansas during the summer of 1909 … No method of contagion could be found, and the author does not consider the disease contagious."

    Flexner & Lewis, 1910 - Multiple unsuccessful polio transmission attempts. "Many guinea-pigs and rabbits, one horse, two calves, three goats, three pigs, three sheep, six rats, six mice, six dogs, and four cats have had active virus introduced in the brain but without causing any appreciable effect whatever. These animals have been under observation for many weeks."

    A Washinton, 1911 - “I have not seen any cases of Polio contagion. We put the patients on one side and typhoid cases on the other, and no nurse or mother was infected. If the disease was so contagious, I don't see why the nurses and mothers would not have been infected.”

    J.J. Moren, 1912 - "Monkeys suffering from polio in the same cage with healthy monkeys, do not infect others."

    P. H. Römer, 1913 - "No proofs of the contagiousness of the disease [polio] could be obtained in the great epidemic in New York in 1907, nor in the epidemic in the Steiermark (Furntratt, Potpeschnigg) nor in Pomerania (Peiper).

    H. W. Frauenthal, 1914 - "Advocates of the contagion theory were at a loss to account for the fact that spontaneous [polio] transmission among laboratory monkeys was never known to occur ... There is no proof that spontaneous transmission of acute poliomyelitis, without an inoculation wound, can take place. There is no proof that contact contagion takes place. Spontaneous development of the disease among laboratory animals is unknown."

    W.H. Frost, 1916 - "The disease [polio] develops in a such a small proportion of people known to have been intimately associated with acute cases of polio." ... "The majority of cases of poliomyelitis can not be traced to known contact, either direct or indirect, with any previous case."

    W. L. Holt, 1916 - Investigated an epidemic of polio and found that he was "surprised that I could trace hardly any cases to personal contact with others, there rarely being successive cases."

    Dr. I. D. Rawlings, 1916 - "Any one who has had much experience with poliomyelitis is struck by the infrequency, relatively, of the secondary cases among direct contacts ... there were approximately 1,500 direct contacts, and yet but one possible case occurred among them. Also among the large number of people that came from New York and other infected areas not a single case occurred.”

    H. L. Abramson, 1917 - Attempts to induce polio in a monkey by injecting the spinal fluid of 40 polio patients (rather than the ground cord) into the brain failed.

    Dold et al. 1917 (Original paper in German from Muenchener Medizinische Wochenschrift 64 ( 1917), bottom of p 143) - Injected healthy people with the nasal secretions taken from one ill person, 1/40 healthy people became ill.

    A review of the investigations concerning the etiology of measels, A. W. Sellards
    harvard Medical School. Boston, Massachusetts as seen below:
    - Jurgelunas, 1914: Tried to produce measles in monkeys using inoculations of the blood and mucus secretions from measles patients as well as by exposing the animals to patients in measles wards. All results were negative.
    - Sellards, 1918: Tried to transmit measles to 8 healthy volunteers without a prior history of measles exposure. 0/8 men became sick after multiple failed attempts.
    - Sellards and Wenworth, 1918: Inoculated 3 monkeys in various ways, including intensive injections of blood from measles patients. The animals remained well.
    - Sellards and Wenworth, 1918: Blood from measles patients was injected simultaneously into 2 men and 2 monkeys. Both men remained symptom-free. One of the two monkeys developed symptoms that were not suggestive of measles.

    Milton Rosenau, 1918 - Professor of preventive medicine and hygiene at Harvard, notes that "monkeys have so far never been known to contract the disease [polio] spontaneously, even though they are kept in intimate association with infected monkeys." Page 341.

    Hess & Unger, 1918 - "In three instances the nasal secretion of varicella patients was applied to the nostrils; in three others the tonsillar secretion to the tonsils, and in six, the tonsillar and pharyngeal secretions were transferred to the nose, the pharynx, and the tonsils. In none of these twelve cases was there any reaction whatsoever, either local or systemic."

    Hess & Unger, 1918 - The vesicle fluids from people with chickenpox was injected intravenously into 38 children. 0/38 became sick.

    Published in the Journal - American Medical Association, 1919 - Need Of Further Research On The Transmissibility Of Measles And Varicella. “Evidently in our experiments we do not, as we believe, pursue nature's mode of transmission; either we fail to carry over the virus, or the path of infection is quite different from what it is commonly thought to be.”

    Milton J. Rosenau, March 1919 - Conducted 9 separate experiments in a group of 49 healthy men, to prove contagion. In all 9 experiments, 0/49 men became sick after being exposed to sick people or the bodily fluids of sick people.

    More information on the Rosenau studies here.

    Wahl et al, 1919 - Conducted 3 separate trials on six men attempting to infect them with different strains of Influenza. Not a single person got sick.

    Schmidt et al, 1920 (Original paper in German here) - Conducted two controlled experiments, exposing healthy people to the bodily fluids of sick people. Of 196 people exposed to the mucous secretions of sick people, 21 (10.7%) developed colds and three developed grippe (1.5%). In the second group, of the 84 healthy people exposed to mucous secretions of sick people, five developed grippe (5.9%) and four colds (4.7%). Of forty-three controls who had been inoculated with sterile physiological salt solutions eight (18.6%) developed colds. A higher percentage of people got sick after being exposed to saline compared to those being exposed to the “virus”.

    Williams et al, 1921 - Tried to experimentally infect 45 healthy men with the common cold and influenza, by exposing them to mucous secretions from sick people. 0/45 became ill.

    Mahatma Gandhi, 1921 - "and the poison that accumulates in the system is expelled in the form of small-pox. If this view is correct, then there is absolutely no need to be afraid of small-pox" also see "This has given rise to the superstition that it is a contagious disease, and hence to the attempt to mislead the people into the belief that vaccination is an effective means of preventing it."

    Blanc and Caminopetros, 1922 (original paper in French here) - Material from nine cases of shingles was inoculated into the eyes, cornea, conjunctiva, skin, brain, and spinal cord of a series of animals, including rabbits, mice, sheep, pigeons, monkeys, and a dog. All results were negative.

    Robertson & Groves, 1924 - Exposed 100 healthy individuals to the bodily secretions from 16 different people suffering from influenza. 0 people of 100 whom they deliberately tried to infect with Influenza got sick That is because Viruses don't cause disease.

    Bauguess, 1924 - "A careful search of the literature does not reveal a case in which the blood from a patient having measles was injected into the blood stream of another person and produced measles."

    The problem of the etiology of herpes zoster, 1925 - "Many other authors report entirely negative results following the inoculation of herpes zoster material into the sacrified corneas of rabbits: Kraupa (18); Baum (19); LSwenstein (8), Teissier, Gastinel, and Reilly (20) ; Kooy (21) ; Netter and Urbain (22); Bloch and Terris (23); Simon and Scott (24); and Doerr (25). It is evident, therefore, that the results of attempts to inoculate animals with material from cases of herpes zoster must be considered at present to be inconclusive."

    Volney S and Chney M.D., 1928 - A study where it is clearly stated that cold is not infectious.

    Dochez et al, 1930 - Attempted to infect 11 men with intranasal influenza. Not a single person got sick. Most strikingly one person got very sick when he accidently found out that is what they were trying to do. His symptoms disappeared when they told him he was misinformed.

    L. L. Lumsden, 1935 - “Painstaking efforts were made throughout the studies to obtain all traces of transmission of the disease through personal contact, but it appears that in this outbreak in Louisville evidence of personal association between the cases of poliomyelitis, suggestive of cause and effect, was no more common than that which might have been found if histories had been taken of personal association between cases of broken bones occurring in the city in the same period.”

    Thomas Francis Jr et al, 1936 - Gave 23 people influenza via 3 different methods. 0 people got sick.. They gave 2 people already "suffering from colds" the influenza who also did not get sick

    Burnet and Lush, 1937 - 200 people given "Melbourne type" Influenza . 0 people showed any symptoms of disease. 200/0.

    Lumsden, 1938 - "It is quite usual in small [polio] outbreaks in rural counties for individual cases to develop in separate homes three or for miles apart without there being any evidence of direct or indirect personal contact having operated between persons afflicted."

    L. L Lumsden, 1938 - ”The general and usual epidemiological features of the disease [polio] all appear opposed to the hypothesis that poliomyelitis is a contagious disease spread among human beings by nose-to-nose or any other direct personal contact.”

    Burnet and Foley, 1940 - Attempted to experimentally infect 15 university students with influenza. The authors concluded their experiment was a failure.

    Thomas Francis Jr, 1940 - Gave 11 people "Epidemic Influenza" 0 people got sick. That is because viruses don't cause disease.

    John Toomey, 1941 - A veteran polio researcher: "no animal gets the disease from another, no matter how intimately exposed."

    A. R. Kendall, 1945 - “The epidemiological facts of poliomyelitis are these: … (2) A majority of cases of clinically diagnosable poliomyelitis (polioparalysis) occur sporadically, with no history of contact with previous cases. (3) Two cases of polioparalysis in one family are unusual, even though no precautions are taken to prevent cross infection. (4) Clinically diagnosable cases of poliomyelitis (polioparalysis) show little tendency to spread, even in schools or other places of public gathering. (5) Incidence of polioparalysis is no greater among doctors and nurses, in intimate contact with acute cases than it is among the civil population, even though the former are exposed freely to infection.” […] “Polioparalysis is not contagious.”

    E. B. Shaw & H. E. Thelander, 1949 - “The epidemiology of the disease [polio] remains obscure. There has been a tendency to depart from an early theory that the disease spreads by means of direct contact.”

    Albert Sabin, 1951 (inventor of the polio vaccine). "There is no evidence for the transmission of poliomyelitis by droplet nuclei."

    Archibald L. Hoyne, 1951 (alternative link here) - “However, in the Cook County Contagious Disease Hospital where the latter procedure has not been used there has never been a doctor, intern, nurse or any other member of the personnel who contracted poliomyelitis within a period of at least thirty-five years, nor has any patient ever developed poliomyelitis after admission to the hospital.”

    Ralph R. Scobey, 1951 - ”Although poliomyelitis is legally a contagious disease, which implies that it is caused by a germ or virus, every attempt has failed conclusively to prove this mandatory requirement of the public health law.” Professor of clinical pediatrics and president of the Poliomyelitis Research Institute, Syracuse, N.Y.

    Ralph R. Scobey, 1952 - "In addition to the failure to prove contagiousness of human poliomyelitis, it has likewise been impossible to prove contagiousness of poliomyelitis in experimental animals."

    Douglas Gordon et al, 1975 - This study gave 10 people English type Influenza and 10 people a placebo. The study was negative. Most telling is they admit that mild symptoms were seen in the placebo group, proving that the inoculation methods cause them.

    Beare et al 1980 (refer to reference 6 in the linked paper). Quote from John J Cannell, 2008 as follows - “An eighth conundrum – one not addressed by Hope-Simpson – is the surprising percentage of seronegative volunteers who either escape infection or develop only minor illness after being experimentally inoculated with a novel influenza virus.”

    Nancy Padian, 1996 - A study which followed 176 discordant couples (1 HIV positive and the other negative) for 10 years. These couples regularly slept together and had unprotected sex. There were no HIV transmissions from the positive partner to the negative partner during the entirety of the study.

    John Treanor et al, 1999 - Gave 108 people Influenza A. Only 35% recorded mild symptoms such as stuffy nose. Unfortunately 35% of the placebo control group also developed mild symptoms proving the methods of inoculation are causing them.

    Bridges et al, 2003 - "Our review found no human experimental studies published in the English-language literature delineating person-to-person transmission of influenza... Thus, most information on human-to-human transmission of influenza comes from studies of human inoculation with influenza virus and observational studies."

    The Virology Journal, 2008 - ”There were five attempts to demonstrate sick-to-well influenza transmission in the desperate days following the pandemic [1918 flu] and all were ’singularly fruitless’ … all five studies failed to support sick-to-well transmission, in spite of having numerous acutely ill influenza patients, in various stages of their illness, carefully cough, spit, and breathe on a combined total of >150 well patients.”

    Public Health Reports, 2010 - ”It seemed that what was acknowledged to be one of the most contagious of communicable diseases [1918 flu] could not be transferred under experimental conditions.”

    Jasmin S Kutter, 2018, - Our observations underscore the urgent need for new knowledge on respiratory virus transmission routes and the implementation of this knowledge in infection control guidelines to advance intervention strategies for currently circulating and newly emerging viruses and to improve public health.
    - There is a substantial lack of (experimental) evidence on the transmission routes of PIV (types 1–4) and HMPV.
    - Extensive human rhinovirus transmission experiments have not led to a widely accepted view on the transmission route [35, 36, 37, 38, 39, 40].
    - However, until today, results on the relative importance of droplet and aerosol transmission of influenza viruses stay inconclusive and hence, there are many reviews intensively discussing this issue [10, 45, 46, 47, 48, 49, 50].
    - Despite this, the relative importance of transmission routes of respiratory viruses is still unclear, depending on the heterogeneity of many factors like the environment (e.g. temperature and humidity), pathogen and host [5, 19].

    Jonathan Van Tam, 2020 - Conducted these human trials of Flu A in 2013. 52 people were intentionally given "Flu A" and made to live in controlled conditions with 75 people. 0 people sick. 0 PCR positive.

    J.S. Kutter, 2021 - “Besides nasal discharge, no other signs of illness were observed in the A/H1N1 virus-positive donor and indirect recipient animals.” The animals were subsequently euthanized after the animals experienced what the scientist describe as having breathing difficulties (no further details were given to describe their condition). *Refer to Note 1.

    Ben Killingley, 2022 - Gave 36 people what he considered to be purified Covid Virus Intranasally. The Results: Nobody got sick. *Refer to Note 2.

    Notes

    *Note 1 - Jasmin Kutter, 2021:

    From the Results section: “Throat and nasal swabs were collected from the donor and indirect recipient animals on alternating days.” This on its own can lead to nasal discharge which is the only “sign of illness” that was noted in this study.

    *Note 2 - Ben Killingley, 2022:

    See the video explanation by Jamie here.

    Ben Killingley also conducted a study in the early 2010's in which he had inoculated people in a room with 75 others some wearing masks others as a control. Not a single person even tested PCR positive. Some links to his previous studies include a 2011, 2019 and a 2020 study.

    It is assumed that his latest, 2022 study, is a follow up to cover the findings of his previous findings. Some additional notes on the study referenced include:

    - They gave 10 people the potent nephrotoxin Remdisivir.

    - They measure sickness by means of a PCR test which isn't indicative of disease because it can tests positive with “asymptomatic” cases as well.

    - Even if you say that a runny nose after swabbing is Covid. A 50% outcome to a direct challenge of something is a negative result. It doesn't suggest causation which would need to be at least 90%.

    - The very methods of inoculation used during the study could cause the nasal congestion/discharge (which is their measure of whether someone is sick or not). This has been shown in previous studies.

    - Lastly nobody was given "regeneron" because nobody got "sick".

    *Note 3 - Dr Robert Willner, 1994:

    December 7th 1994 Hollywood Roosevelt Hotel, Greensboro, N.C., Dr Willner (a medical doctor of 40 years experience) an outspoken whistleblower of the AIDS hoax. In front of a gathering of about 30 alternative-medicine practitioners and several journalists, Willner stuck a needle in the finger of Andres, 27, a Fort Lauderdale student who says he has tested positive for HIV. Then, wincing, the 65-year-old doctor stuck himself. In 1993, Dr. Willner stunned Spain by inoculating himself with the blood of Pedro Tocino, an HIV positive hemophiliac. This demonstration of devotion to the truth and the Hippocratic Oath he took, nearly 40 years before, was reported on the front page of every major newspaper in Spain. His appearance on Spain’s most popular television show envoked a 4 to 1 response by the viewing audience in favor of his position against the “AIDS hypothesis.” When asked why he would put his life on the line to make a point, Dr. Willner replied: “I do this to put a stop to the greatest murderous fraud in medical history. By injecting myself with HIV positive blood, I am proving the point as Dr. Walter Reed did to prove the truth about yellow fever. In this way it is my hope to expose the truth about HIV in the interest of all mankind.” He tested negative multiple times. He died of a Heart attack 4 months later 15th April 1995 (yeh right, funny how these naysayers all die suddenly. Link to the presentation here.

    Ludicrous “Transmission” Studies

    The picture of virology’s ludicrousy won’t be complete without a list of studies showing the insanity of what virologists claim to be transmission of disease. This include the injection of fluids into the brains and lungs of animals and we may just include some epidemiological studies to show how these are also not proof of anything. Joe Hendry mostly put it together and the papers we have are as follows (*Please note that this section is open to comments at the moment and anyone that want to add notes or studies are free to leave a comment):

    Louis Pasteur, 1881 - For rabies, tried to demonstrate transmission by injecting diseased brain tissue "directly onto the surface of the brain of a healthy dog through a hole drilled into its skull."

    Simon Flexner and Paul A. Lewis, 1910 - Spinal cords from deceased children were ground up and emulsified to be injected into the brains of monkeys. Study explained in detail here.

    John F. Anderson and Joseph Goldberger, 1911 - Injected blood from a measles patient directly into the heart and brains of monkeys.

    Carl Tenbroeck, 1918 - A mixture of ground up rat's livers, spleens, kidneys,
    testicles, lungs, hearts, and brains was injected into the brains of other rats.

    Claus W. Jungeblut, 1931 - Ground up monkey spinal cord was injected into the brains of other monkeys.

    Wilson Smith, 1933 - “The infected animal is killed when showing symptoms, often at the beginning of the second temperature rise. The turbinates are scraped out, ground up with sand, and emulsified in about 20 c.cm. of equal parts of broth and saline. The emulsion is lightly centrifuged, and about 1 c.cm. of the supernatant fluid is dropped into the nostrils of another ferret.”

    Thomas Francis and Jr, T. P. Magill, 1935 - Ground up ferret lung tissue was injected into the brains of rabbits.

    Ann G. Kuttner and T'sun T'ung, 1935 - Ground up kidney and brain of a guinea pig was injected into the brain of another guinea pig.

    Erich Traub. April 01 1936 - Ground up mouse brain was injected into the brains of guinea pigs.

    Albert B. Sabin and Peter K. Olitsky, 1937 - Ground up mouse brain was injected into the brains of other mice.

    G. John Buddingh, 1938 - Ground up chick embryo was injected into the brains 2 or 3 day old chicks.

    Gilbert Dalldorf, 1939 - Ground up ferret spleens was injected into the brains of mice.

    Claus W. Jungeblut et al, 1942 - Ground up brain or spinal cord of paralyzed mice was injected into the brains of 13 monkeys.

    Henry Pinkerton and Vicente Moragues, 1942 - Ground up brain tissue from dying mice was injected into the brains of pigeons.

    C. Kling et al, 1942 - Injected sewage sludge into the brains and abdomen of monkeys. This convinced him that he had isolated a virus and proven that the sewer is a vehicle for polio transmission.

    D.M. Horstmann, 1944 - Allegedly "proved" that the feces of polio patients contained "poliovirus" by injecting fecal samples into monkeys' brains and spines.

    Joseph E. Smadel et al, 1945 - Ground up pigeon spleen was injected into the brains of mice.

    F. Sargent Cheever et al, 1949 - Ground up mouse brain was injected into the brains of rats and hamsters.

    Isolation

    Isolation has been well defined in Virus Lie - The Result of 4 Years of Study and to this day there has not been a single paper presented that could show the isolation of a virus without first contaminating the sample. This is shown in detail in the virus lie article and will not be repeated here again. One interesting point that can be captured here is all the studies showing a control test proving that the isolation method used for viruses is flawed. They can be listed as follows:

    John F Enders, 1954 - Under other agents isolated during the study. "A second agent was obtained from an uninoculated culture of monkey kidney cells. The cytopathic changes it induced in the unstained preparations could not be distinguished with confidence from the viruses isolated from measles." It is highlighted here. Refer to the video explanation here.

    Image
    It is further discussed in the paper that "While there is no ground for concluding that the factors in vivo (in the body) are the same as those which underlie the formation of giant cells and the nuclear disturbances in vitro (outside a living organism), the appearance of these phenomena in cultured cells is consistent with the properties that a priori might be associated with the virus of measles.”

    Image
    Rustigian et al, 1955 - This paper is described in an article by Viroliegy here (look under Rustigain in the article).

    Cohen et al, 1955 - This paper is also described in the same article by Viroliegy here (look under Cohen in the article).

    Bech and von Magnus, 1959 - This paper is also described in the same article by Viroliegy here (look under Von Magnus in the article).

    F Rapp et al, 1959 - This paper is described in a video by Spacebusters here. Most noteworthy is “Monkey kidney cells, however, are unsuitable for the investigations of the type reported here; Peebles et al. and Ruckle showed that monkeys, and cell cultures derived from them, are often infected with an agent serologically indistinguishable from human measles virus, which causes cytopathic changes in monkey kidney cell cultures almost identical with those caused by human measles virus.”

    Image
    Carl J. O’Hara et al, 1988 - The study demonstrated "HIV" particles in 18 out of 20 (90% of) AIDS-related lymph node enlargements but also in 13 out of 15 (88% of) non-AIDS-related enlargements. Which means that particles claimed to be HIV virions are non-specific since identical particles can be found in the majority of patients with enlarged lymph nodes not attributed to AIDS, and at no risk for developing AIDS. Refer to @Aldhissla45’s tweet here.

    P Gluschankof et al, 1997 - This paper described in a video here with additional notes by Jamie here.

    Julian W. Bess Jr., 1997 - This paper described in a video here with additional notes by Jamie here.

    C.A. Cassol, 2020 - This paper is described by Andrew Kaufman here as well as by Thomas Cowan here.

    “Unofficially” we can also add the Lanka 3 phase control experiment that can be seen here or searched for it here.

    A further indication of the isolation procedure fallacy is shown in a study during which the CPE becomes more well defined with the addition of specific substances. The study is as follows:

    Leon Caly et al, 2020 - “Following several failures to recover virions with the characteristic fringes of surface spike proteins, it was found that adding trypsin to the cell culture medium immediately improved virion morphology.” See a video explanation here.

    Recent Requests and Statements

    Further and more recent requests and statements that were sent to me by my good friend Courtenay are as follows:

    May 5, 2022:
    U.S. CDC and Agency for Toxic Substances and Disease Registry confirmed that a search of their records failed to find any that describe anyone on Earth finding an alleged “avian influenza virus” in the bodily fluids of any diseased diseased host (animal or human) and purifying “it”… which is necessary so that “it” could be sequenced, characterized and studied with controlled experiments. This can be viewed here.

    May 20, 2022:
    Public Health Agency of Canada confirmed that they have no record of any alleged “avian influenza virus” having been found and purified from the bodily fluid/tissue/excrement of any diseased “host” on the planet (in order for “it” to be sequenced, characterized and studied with controlled experiments) by anyone, anywhere, ever.
    Insanely, they insist that:

    “Viruses” are in hosts despite their utter inability to find them there,.

    It’s necessary to “grow them” in non-host cells (as if “they” would grow better there than they allegedly grew in the diseased host lol).

    They pretend that mixing complex substances together results in purification.

    This can be viewed here.

    December 20, 2021:
    Public Health Agency of Canada confirmed that they have no record of any alleged “virus” having been purified from a sample taken from any diseased human on Earth, by anyone, ever, period. To be viewed here.

    March 11, 2022:
    U.S. Centers for Disease Control and Prevention and Agency for Toxic Substances and Disease Registry respond to a FOIA request for all studies / reports in their possession, custody or control describing the purification of any “virus” addressed by any “vaccine” on either their childhood or adult U.S. “immunization” schedule, directly from a sample taken from any diseased "host" on Earth where the sample was not first combined with any other source of genetic material. CDC/ATSDR provided 5 studies on “rotavirus” (thereby admitting they have no records for any other alleged viruses). None of these 5 studies actually describe isolation/purification of a “rotavirus” from a human.
    Request, response, studies to be viewed here.

    March 8, 2023:
    Italy 2020: Inside Covid’s “Ground zero” in Europe - Three years ago the Western World came to a standstill. The official Covid-19 narrative depicted a strange suddenly-super-spreading, deadlier-than-flu virus hailing from China that landed in Northern Italy.

    On February 20, 2020 the first alleged case of Covid-19 was discovered in the West in the Lombardy town of Codogno, Italy. Later that day the Italian government reported their first “Covid-19 death.”

    Dramatic media reports emerging from Northern Italy were hammered into and onto the Western psyche giving the impression there was a mysterious “super spreading” and “super lethal” novel virus galloping across the region infecting and killing scores of people.

    Read the rest of the report here.

    Conclusion

    The above list will be worked on over the coming years. If you think that any corrections need to be made or if you want to add additional studies, please leave a comment.


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    https://open.substack.com/pub/dpl003/p/virology-the-damning-evidence?r=29hg4d&utm_medium=ios&utm_campaign=post
    Virology - The Damning Evidence The Stake In The Heart For This Pseudoscientific Profession dpl Introduction One never realize how big the task of writing on a subject is until you start. One thing you can be assured of is how much you learn by writing about your findings or thoughts. My stance on virology has been clarified in two previous posts as follows: The Gatekeepers Club. Virus Lie - The Result of 4 Years of Study. Another thing you quickly realize on this journey is how easy it is to censor someone, especially if you start hitting a nerve. I have documented some of it underneath the conclusion of the The Gatekeepers Club article. It is very important to make copies of your work, as shadow banning is one thing, but if these platforms decide to terminate your channel and all the work you have done is on it, you will obviously lose it all. We were in that same position about a year ago when Discord decided to terminate our channel. Twenty of the smartest people you would ever know had been working on it for close to two years, and it was gone overnight. Therefore, this post will serve as safekeeping for some of the best information that I have come across in the last few weeks proving that virology is pseudoscience. Update - 18 September 2023 The order of the sections of this article has been rearranged to introduce the most important information first. As mentioned in my most recent article titled: Hacking at the Root of the Virus Issue it was explained that for the longest time I thought that failure to “isolate” viruses was the most important evidence to focus on. This is however not the case as explained in detail in the “Hacking at the Root of the Virus Issue” article. Transmission is the fundamental assumption on which virology rest. Without proof of transmission, nothing downstream matters. Even though understanding these downstream concepts will never be a waste of time one must consider that the normal man on the street will not be interested in complicated terminology and processes. It is of crucial importance for the no virus community to find easier ways to explain the fallacy that is virology. Seeing as no one need a laboratory to assess whether transmission is possible and because we can observe this phenomena ourselves (Inductive reasoning) this is the linchpin for virology. A twitter space where we discussed this can be viewed here (*Note: Jamie was cut off during his talk and his section was not included). As discussed during the twitter space, we have reviewed the available transmission studies and a summary of these studies can be seen below. Transmission / Infection One of the funniest things you will see while debating the trolls on Twitter is that they will provide studies conducted to prove the efficacy of vaccines. The people that undertake these studies assume that transmission or infection has already been proven, but nothing could be further from the truth. That is why it is important for us to list the peer-reviewed studies that disprove transmission or infection to further demonstrate that virology is a pseudoscience. The list of studies was compiled with the help of Jamie, georgie&donny, and Aldhissla (also see Aldhissla’s list on polio here). (*Please note that this section is open to comments at the moment and anyone that want to add notes or studies are free to leave a comment). The Journal of Infectious Diseases, Vol. 2, No. 2 (Mar. 1, 1905): - Chapman, 1801: Tried to transmit measles using the blood, tears, the mucus of the nostrils and bronchia, and the eruptive matter in the cuticle without any success. - Willan, 1809: Inoculated three children with vesicle fluids of measles but without success. - Albers, 1834: Attempted to infect four children with measles without success. He quoted Alexander Monro, Bourgois, and Spray as also having made unsuccessful inoculations with saliva, tears, and cutaneous scales. - Themmen, 1817: Tried to infect 5 children with measles. 0/5 children became sick. Charles Creighton, 1837 (A history of epidemics in Britain). "No proof of the existence of any contagious principles by which it was propagated from one individual to another." EH Ackernecht, writing about Anticontagionism between 1821 and 1867 - “That the anticontagionists were usually honest men and in deadly earnest is shown, among other things, by the numerous self-experiments to which they submitted themselves to prove their contentions.” also see “Famous are the plague self-experiments of Clot-Bey, the offers for plague self-experiment by Chervin, Lassis, Costa, Lapis, and Lasserre, and the cholera self-experiments of Fay, Scipio Pinel, Wayrot, and J.L. Guyon. The amazing thing is that almost all of these experiments failed to produce the disease.” Note on Hospitals by Florence Nightingale, 1858 - "Suffice it to say, that in the ordinary sense of the word, there is no proof, such as would be admitted in any scientific inquiry, that there is any such thing as 'contagion." also see "Just as there is no such thing as 'contagion,' there is no such thing as inevitable 'infection." Andreas Christian Bull, 1868 - “It does not seem apparent in this small [polio] epidemic that contagion played any role, because the disease occurred here and there in the different places of the district without the possibility of establishing any relation between the various cases or the families of the same.” Karl-Oskar Medin, 1887 - A Swedish pediatrician who was the first to examine a polio outbreak, concluded that it was an infectious, but not contagious, disease. Charles Caverly, 1894 - Investigated the first US polio epidemic: ”it is very certain that it was non-contagious.” Journal of American Medical Association, Volume 72, Number 3, 1919 (or additional link here): - Warschawsky, 1895 - Injected small pigs and rabbits with blood taken in the eruptive stage. All results were negative. - Belila, 1896 - Placed warm nasal mucus and saliva from measles patients on the nasal and oral mucous membrane of rabbits, guinea-pigs, cats, mice, dogs and lambs, but without any positive results. - Josias, 1898 - Rubbed measles secretions over the throat, nose and eyes of several young pigs, but without any effects. - Geissler, 1903 - Inoculated sheep, swine, goats, dogs and cats in various ways with the bodily fluids from patients with measles; including smearing, spraying, rubbing. All results were negative. - Pomjalowsky, 1914 - Injected measles blood into guineapigs, rabbits and small pigs. All results were negative. - Jurgelunas, 1914 - Inoculated blood from patients with measles into suckling pigs and rabbits, but without effect. Leegaard, 1899 - Was not able to prove a single case of patient-to-patient contagion in a polio outbreak in Norway. "Infantile paralysis is of an infectious, but not of a contagious nature. As a matter of fact no indisputable instance of contagion could be proved." Dr. Rodermund, 1901 - From his diary of SmallPox experiments. For 15 years he smeared the pus of smallpox patients on his face and used to go home with his family, play cards at the gentleman’s club and treat other patients and never got sick or saw a single other person get sick. Walter Reed, 1902 - “Without entering into details, I may say that, in the first place, the Commission saw, with some surprise, what had so often been noted in the literature, that patients in all stages of yellow fever could be cared for by non-immune nurses without danger of contracting the disease. The non-contagious character of yellow fever was, therefore, hardly to be questioned.” Landsteiner & Popper, 1909 - "Attempts to transmit the disease [polio] to the usual laboratory animals, such as rabbits, guinea pigs, or mice, failed." F.E. Batten, (1909) - “Against the infectivity of the disease may be urged, first, the absence of spread of infection in hospital. The cases of poliomyelitis admitted to hospital freely mixed with other cases in the ward without any isolation or disinfection, some 70 children came in contact, but no infection took place. (p. 208, last paragraph)” The Boston medical and surgical journal, 1909 - An inquiry a 1908 polio outbreak found the following: “A large number of children were in intimate contact with those that were sick, and of these children an insignificant minority developed the disease.” 244 children were in intimate contact with those who were afflicted with polio. Of those 244 children, an "insignificant minority" developed the disease. Massachusetts State board of health, 1909 - "Poliomyelitis prevailed in epidemic form in Kansas during the summer of 1909 … No method of contagion could be found, and the author does not consider the disease contagious." Flexner & Lewis, 1910 - Multiple unsuccessful polio transmission attempts. "Many guinea-pigs and rabbits, one horse, two calves, three goats, three pigs, three sheep, six rats, six mice, six dogs, and four cats have had active virus introduced in the brain but without causing any appreciable effect whatever. These animals have been under observation for many weeks." A Washinton, 1911 - “I have not seen any cases of Polio contagion. We put the patients on one side and typhoid cases on the other, and no nurse or mother was infected. If the disease was so contagious, I don't see why the nurses and mothers would not have been infected.” J.J. Moren, 1912 - "Monkeys suffering from polio in the same cage with healthy monkeys, do not infect others." P. H. Römer, 1913 - "No proofs of the contagiousness of the disease [polio] could be obtained in the great epidemic in New York in 1907, nor in the epidemic in the Steiermark (Furntratt, Potpeschnigg) nor in Pomerania (Peiper). H. W. Frauenthal, 1914 - "Advocates of the contagion theory were at a loss to account for the fact that spontaneous [polio] transmission among laboratory monkeys was never known to occur ... There is no proof that spontaneous transmission of acute poliomyelitis, without an inoculation wound, can take place. There is no proof that contact contagion takes place. Spontaneous development of the disease among laboratory animals is unknown." W.H. Frost, 1916 - "The disease [polio] develops in a such a small proportion of people known to have been intimately associated with acute cases of polio." ... "The majority of cases of poliomyelitis can not be traced to known contact, either direct or indirect, with any previous case." W. L. Holt, 1916 - Investigated an epidemic of polio and found that he was "surprised that I could trace hardly any cases to personal contact with others, there rarely being successive cases." Dr. I. D. Rawlings, 1916 - "Any one who has had much experience with poliomyelitis is struck by the infrequency, relatively, of the secondary cases among direct contacts ... there were approximately 1,500 direct contacts, and yet but one possible case occurred among them. Also among the large number of people that came from New York and other infected areas not a single case occurred.” H. L. Abramson, 1917 - Attempts to induce polio in a monkey by injecting the spinal fluid of 40 polio patients (rather than the ground cord) into the brain failed. Dold et al. 1917 (Original paper in German from Muenchener Medizinische Wochenschrift 64 ( 1917), bottom of p 143) - Injected healthy people with the nasal secretions taken from one ill person, 1/40 healthy people became ill. A review of the investigations concerning the etiology of measels, A. W. Sellards harvard Medical School. Boston, Massachusetts as seen below: - Jurgelunas, 1914: Tried to produce measles in monkeys using inoculations of the blood and mucus secretions from measles patients as well as by exposing the animals to patients in measles wards. All results were negative. - Sellards, 1918: Tried to transmit measles to 8 healthy volunteers without a prior history of measles exposure. 0/8 men became sick after multiple failed attempts. - Sellards and Wenworth, 1918: Inoculated 3 monkeys in various ways, including intensive injections of blood from measles patients. The animals remained well. - Sellards and Wenworth, 1918: Blood from measles patients was injected simultaneously into 2 men and 2 monkeys. Both men remained symptom-free. One of the two monkeys developed symptoms that were not suggestive of measles. Milton Rosenau, 1918 - Professor of preventive medicine and hygiene at Harvard, notes that "monkeys have so far never been known to contract the disease [polio] spontaneously, even though they are kept in intimate association with infected monkeys." Page 341. Hess & Unger, 1918 - "In three instances the nasal secretion of varicella patients was applied to the nostrils; in three others the tonsillar secretion to the tonsils, and in six, the tonsillar and pharyngeal secretions were transferred to the nose, the pharynx, and the tonsils. In none of these twelve cases was there any reaction whatsoever, either local or systemic." Hess & Unger, 1918 - The vesicle fluids from people with chickenpox was injected intravenously into 38 children. 0/38 became sick. Published in the Journal - American Medical Association, 1919 - Need Of Further Research On The Transmissibility Of Measles And Varicella. “Evidently in our experiments we do not, as we believe, pursue nature's mode of transmission; either we fail to carry over the virus, or the path of infection is quite different from what it is commonly thought to be.” Milton J. Rosenau, March 1919 - Conducted 9 separate experiments in a group of 49 healthy men, to prove contagion. In all 9 experiments, 0/49 men became sick after being exposed to sick people or the bodily fluids of sick people. More information on the Rosenau studies here. Wahl et al, 1919 - Conducted 3 separate trials on six men attempting to infect them with different strains of Influenza. Not a single person got sick. Schmidt et al, 1920 (Original paper in German here) - Conducted two controlled experiments, exposing healthy people to the bodily fluids of sick people. Of 196 people exposed to the mucous secretions of sick people, 21 (10.7%) developed colds and three developed grippe (1.5%). In the second group, of the 84 healthy people exposed to mucous secretions of sick people, five developed grippe (5.9%) and four colds (4.7%). Of forty-three controls who had been inoculated with sterile physiological salt solutions eight (18.6%) developed colds. A higher percentage of people got sick after being exposed to saline compared to those being exposed to the “virus”. Williams et al, 1921 - Tried to experimentally infect 45 healthy men with the common cold and influenza, by exposing them to mucous secretions from sick people. 0/45 became ill. Mahatma Gandhi, 1921 - "and the poison that accumulates in the system is expelled in the form of small-pox. If this view is correct, then there is absolutely no need to be afraid of small-pox" also see "This has given rise to the superstition that it is a contagious disease, and hence to the attempt to mislead the people into the belief that vaccination is an effective means of preventing it." Blanc and Caminopetros, 1922 (original paper in French here) - Material from nine cases of shingles was inoculated into the eyes, cornea, conjunctiva, skin, brain, and spinal cord of a series of animals, including rabbits, mice, sheep, pigeons, monkeys, and a dog. All results were negative. Robertson & Groves, 1924 - Exposed 100 healthy individuals to the bodily secretions from 16 different people suffering from influenza. 0 people of 100 whom they deliberately tried to infect with Influenza got sick That is because Viruses don't cause disease. Bauguess, 1924 - "A careful search of the literature does not reveal a case in which the blood from a patient having measles was injected into the blood stream of another person and produced measles." The problem of the etiology of herpes zoster, 1925 - "Many other authors report entirely negative results following the inoculation of herpes zoster material into the sacrified corneas of rabbits: Kraupa (18); Baum (19); LSwenstein (8), Teissier, Gastinel, and Reilly (20) ; Kooy (21) ; Netter and Urbain (22); Bloch and Terris (23); Simon and Scott (24); and Doerr (25). It is evident, therefore, that the results of attempts to inoculate animals with material from cases of herpes zoster must be considered at present to be inconclusive." Volney S and Chney M.D., 1928 - A study where it is clearly stated that cold is not infectious. Dochez et al, 1930 - Attempted to infect 11 men with intranasal influenza. Not a single person got sick. Most strikingly one person got very sick when he accidently found out that is what they were trying to do. His symptoms disappeared when they told him he was misinformed. L. L. Lumsden, 1935 - “Painstaking efforts were made throughout the studies to obtain all traces of transmission of the disease through personal contact, but it appears that in this outbreak in Louisville evidence of personal association between the cases of poliomyelitis, suggestive of cause and effect, was no more common than that which might have been found if histories had been taken of personal association between cases of broken bones occurring in the city in the same period.” Thomas Francis Jr et al, 1936 - Gave 23 people influenza via 3 different methods. 0 people got sick.. They gave 2 people already "suffering from colds" the influenza who also did not get sick Burnet and Lush, 1937 - 200 people given "Melbourne type" Influenza . 0 people showed any symptoms of disease. 200/0. Lumsden, 1938 - "It is quite usual in small [polio] outbreaks in rural counties for individual cases to develop in separate homes three or for miles apart without there being any evidence of direct or indirect personal contact having operated between persons afflicted." L. L Lumsden, 1938 - ”The general and usual epidemiological features of the disease [polio] all appear opposed to the hypothesis that poliomyelitis is a contagious disease spread among human beings by nose-to-nose or any other direct personal contact.” Burnet and Foley, 1940 - Attempted to experimentally infect 15 university students with influenza. The authors concluded their experiment was a failure. Thomas Francis Jr, 1940 - Gave 11 people "Epidemic Influenza" 0 people got sick. That is because viruses don't cause disease. John Toomey, 1941 - A veteran polio researcher: "no animal gets the disease from another, no matter how intimately exposed." A. R. Kendall, 1945 - “The epidemiological facts of poliomyelitis are these: … (2) A majority of cases of clinically diagnosable poliomyelitis (polioparalysis) occur sporadically, with no history of contact with previous cases. (3) Two cases of polioparalysis in one family are unusual, even though no precautions are taken to prevent cross infection. (4) Clinically diagnosable cases of poliomyelitis (polioparalysis) show little tendency to spread, even in schools or other places of public gathering. (5) Incidence of polioparalysis is no greater among doctors and nurses, in intimate contact with acute cases than it is among the civil population, even though the former are exposed freely to infection.” […] “Polioparalysis is not contagious.” E. B. Shaw & H. E. Thelander, 1949 - “The epidemiology of the disease [polio] remains obscure. There has been a tendency to depart from an early theory that the disease spreads by means of direct contact.” Albert Sabin, 1951 (inventor of the polio vaccine). "There is no evidence for the transmission of poliomyelitis by droplet nuclei." Archibald L. Hoyne, 1951 (alternative link here) - “However, in the Cook County Contagious Disease Hospital where the latter procedure has not been used there has never been a doctor, intern, nurse or any other member of the personnel who contracted poliomyelitis within a period of at least thirty-five years, nor has any patient ever developed poliomyelitis after admission to the hospital.” Ralph R. Scobey, 1951 - ”Although poliomyelitis is legally a contagious disease, which implies that it is caused by a germ or virus, every attempt has failed conclusively to prove this mandatory requirement of the public health law.” Professor of clinical pediatrics and president of the Poliomyelitis Research Institute, Syracuse, N.Y. Ralph R. Scobey, 1952 - "In addition to the failure to prove contagiousness of human poliomyelitis, it has likewise been impossible to prove contagiousness of poliomyelitis in experimental animals." Douglas Gordon et al, 1975 - This study gave 10 people English type Influenza and 10 people a placebo. The study was negative. Most telling is they admit that mild symptoms were seen in the placebo group, proving that the inoculation methods cause them. Beare et al 1980 (refer to reference 6 in the linked paper). Quote from John J Cannell, 2008 as follows - “An eighth conundrum – one not addressed by Hope-Simpson – is the surprising percentage of seronegative volunteers who either escape infection or develop only minor illness after being experimentally inoculated with a novel influenza virus.” Nancy Padian, 1996 - A study which followed 176 discordant couples (1 HIV positive and the other negative) for 10 years. These couples regularly slept together and had unprotected sex. There were no HIV transmissions from the positive partner to the negative partner during the entirety of the study. John Treanor et al, 1999 - Gave 108 people Influenza A. Only 35% recorded mild symptoms such as stuffy nose. Unfortunately 35% of the placebo control group also developed mild symptoms proving the methods of inoculation are causing them. Bridges et al, 2003 - "Our review found no human experimental studies published in the English-language literature delineating person-to-person transmission of influenza... Thus, most information on human-to-human transmission of influenza comes from studies of human inoculation with influenza virus and observational studies." The Virology Journal, 2008 - ”There were five attempts to demonstrate sick-to-well influenza transmission in the desperate days following the pandemic [1918 flu] and all were ’singularly fruitless’ … all five studies failed to support sick-to-well transmission, in spite of having numerous acutely ill influenza patients, in various stages of their illness, carefully cough, spit, and breathe on a combined total of >150 well patients.” Public Health Reports, 2010 - ”It seemed that what was acknowledged to be one of the most contagious of communicable diseases [1918 flu] could not be transferred under experimental conditions.” Jasmin S Kutter, 2018, - Our observations underscore the urgent need for new knowledge on respiratory virus transmission routes and the implementation of this knowledge in infection control guidelines to advance intervention strategies for currently circulating and newly emerging viruses and to improve public health. - There is a substantial lack of (experimental) evidence on the transmission routes of PIV (types 1–4) and HMPV. - Extensive human rhinovirus transmission experiments have not led to a widely accepted view on the transmission route [35, 36, 37, 38, 39, 40]. - However, until today, results on the relative importance of droplet and aerosol transmission of influenza viruses stay inconclusive and hence, there are many reviews intensively discussing this issue [10, 45, 46, 47, 48, 49, 50]. - Despite this, the relative importance of transmission routes of respiratory viruses is still unclear, depending on the heterogeneity of many factors like the environment (e.g. temperature and humidity), pathogen and host [5, 19]. Jonathan Van Tam, 2020 - Conducted these human trials of Flu A in 2013. 52 people were intentionally given "Flu A" and made to live in controlled conditions with 75 people. 0 people sick. 0 PCR positive. J.S. Kutter, 2021 - “Besides nasal discharge, no other signs of illness were observed in the A/H1N1 virus-positive donor and indirect recipient animals.” The animals were subsequently euthanized after the animals experienced what the scientist describe as having breathing difficulties (no further details were given to describe their condition). *Refer to Note 1. Ben Killingley, 2022 - Gave 36 people what he considered to be purified Covid Virus Intranasally. The Results: Nobody got sick. *Refer to Note 2. Notes *Note 1 - Jasmin Kutter, 2021: From the Results section: “Throat and nasal swabs were collected from the donor and indirect recipient animals on alternating days.” This on its own can lead to nasal discharge which is the only “sign of illness” that was noted in this study. *Note 2 - Ben Killingley, 2022: See the video explanation by Jamie here. Ben Killingley also conducted a study in the early 2010's in which he had inoculated people in a room with 75 others some wearing masks others as a control. Not a single person even tested PCR positive. Some links to his previous studies include a 2011, 2019 and a 2020 study. It is assumed that his latest, 2022 study, is a follow up to cover the findings of his previous findings. Some additional notes on the study referenced include: - They gave 10 people the potent nephrotoxin Remdisivir. - They measure sickness by means of a PCR test which isn't indicative of disease because it can tests positive with “asymptomatic” cases as well. - Even if you say that a runny nose after swabbing is Covid. A 50% outcome to a direct challenge of something is a negative result. It doesn't suggest causation which would need to be at least 90%. - The very methods of inoculation used during the study could cause the nasal congestion/discharge (which is their measure of whether someone is sick or not). This has been shown in previous studies. - Lastly nobody was given "regeneron" because nobody got "sick". *Note 3 - Dr Robert Willner, 1994: December 7th 1994 Hollywood Roosevelt Hotel, Greensboro, N.C., Dr Willner (a medical doctor of 40 years experience) an outspoken whistleblower of the AIDS hoax. In front of a gathering of about 30 alternative-medicine practitioners and several journalists, Willner stuck a needle in the finger of Andres, 27, a Fort Lauderdale student who says he has tested positive for HIV. Then, wincing, the 65-year-old doctor stuck himself. In 1993, Dr. Willner stunned Spain by inoculating himself with the blood of Pedro Tocino, an HIV positive hemophiliac. This demonstration of devotion to the truth and the Hippocratic Oath he took, nearly 40 years before, was reported on the front page of every major newspaper in Spain. His appearance on Spain’s most popular television show envoked a 4 to 1 response by the viewing audience in favor of his position against the “AIDS hypothesis.” When asked why he would put his life on the line to make a point, Dr. Willner replied: “I do this to put a stop to the greatest murderous fraud in medical history. By injecting myself with HIV positive blood, I am proving the point as Dr. Walter Reed did to prove the truth about yellow fever. In this way it is my hope to expose the truth about HIV in the interest of all mankind.” He tested negative multiple times. He died of a Heart attack 4 months later 15th April 1995 (yeh right, funny how these naysayers all die suddenly. Link to the presentation here. Ludicrous “Transmission” Studies The picture of virology’s ludicrousy won’t be complete without a list of studies showing the insanity of what virologists claim to be transmission of disease. This include the injection of fluids into the brains and lungs of animals and we may just include some epidemiological studies to show how these are also not proof of anything. Joe Hendry mostly put it together and the papers we have are as follows (*Please note that this section is open to comments at the moment and anyone that want to add notes or studies are free to leave a comment): Louis Pasteur, 1881 - For rabies, tried to demonstrate transmission by injecting diseased brain tissue "directly onto the surface of the brain of a healthy dog through a hole drilled into its skull." Simon Flexner and Paul A. Lewis, 1910 - Spinal cords from deceased children were ground up and emulsified to be injected into the brains of monkeys. Study explained in detail here. John F. Anderson and Joseph Goldberger, 1911 - Injected blood from a measles patient directly into the heart and brains of monkeys. Carl Tenbroeck, 1918 - A mixture of ground up rat's livers, spleens, kidneys, testicles, lungs, hearts, and brains was injected into the brains of other rats. Claus W. Jungeblut, 1931 - Ground up monkey spinal cord was injected into the brains of other monkeys. Wilson Smith, 1933 - “The infected animal is killed when showing symptoms, often at the beginning of the second temperature rise. The turbinates are scraped out, ground up with sand, and emulsified in about 20 c.cm. of equal parts of broth and saline. The emulsion is lightly centrifuged, and about 1 c.cm. of the supernatant fluid is dropped into the nostrils of another ferret.” Thomas Francis and Jr, T. P. Magill, 1935 - Ground up ferret lung tissue was injected into the brains of rabbits. Ann G. Kuttner and T'sun T'ung, 1935 - Ground up kidney and brain of a guinea pig was injected into the brain of another guinea pig. Erich Traub. April 01 1936 - Ground up mouse brain was injected into the brains of guinea pigs. Albert B. Sabin and Peter K. Olitsky, 1937 - Ground up mouse brain was injected into the brains of other mice. G. John Buddingh, 1938 - Ground up chick embryo was injected into the brains 2 or 3 day old chicks. Gilbert Dalldorf, 1939 - Ground up ferret spleens was injected into the brains of mice. Claus W. Jungeblut et al, 1942 - Ground up brain or spinal cord of paralyzed mice was injected into the brains of 13 monkeys. Henry Pinkerton and Vicente Moragues, 1942 - Ground up brain tissue from dying mice was injected into the brains of pigeons. C. Kling et al, 1942 - Injected sewage sludge into the brains and abdomen of monkeys. This convinced him that he had isolated a virus and proven that the sewer is a vehicle for polio transmission. D.M. Horstmann, 1944 - Allegedly "proved" that the feces of polio patients contained "poliovirus" by injecting fecal samples into monkeys' brains and spines. Joseph E. Smadel et al, 1945 - Ground up pigeon spleen was injected into the brains of mice. F. Sargent Cheever et al, 1949 - Ground up mouse brain was injected into the brains of rats and hamsters. Isolation Isolation has been well defined in Virus Lie - The Result of 4 Years of Study and to this day there has not been a single paper presented that could show the isolation of a virus without first contaminating the sample. This is shown in detail in the virus lie article and will not be repeated here again. One interesting point that can be captured here is all the studies showing a control test proving that the isolation method used for viruses is flawed. They can be listed as follows: John F Enders, 1954 - Under other agents isolated during the study. "A second agent was obtained from an uninoculated culture of monkey kidney cells. The cytopathic changes it induced in the unstained preparations could not be distinguished with confidence from the viruses isolated from measles." It is highlighted here. Refer to the video explanation here. Image It is further discussed in the paper that "While there is no ground for concluding that the factors in vivo (in the body) are the same as those which underlie the formation of giant cells and the nuclear disturbances in vitro (outside a living organism), the appearance of these phenomena in cultured cells is consistent with the properties that a priori might be associated with the virus of measles.” Image Rustigian et al, 1955 - This paper is described in an article by Viroliegy here (look under Rustigain in the article). Cohen et al, 1955 - This paper is also described in the same article by Viroliegy here (look under Cohen in the article). Bech and von Magnus, 1959 - This paper is also described in the same article by Viroliegy here (look under Von Magnus in the article). F Rapp et al, 1959 - This paper is described in a video by Spacebusters here. Most noteworthy is “Monkey kidney cells, however, are unsuitable for the investigations of the type reported here; Peebles et al. and Ruckle showed that monkeys, and cell cultures derived from them, are often infected with an agent serologically indistinguishable from human measles virus, which causes cytopathic changes in monkey kidney cell cultures almost identical with those caused by human measles virus.” Image Carl J. O’Hara et al, 1988 - The study demonstrated "HIV" particles in 18 out of 20 (90% of) AIDS-related lymph node enlargements but also in 13 out of 15 (88% of) non-AIDS-related enlargements. Which means that particles claimed to be HIV virions are non-specific since identical particles can be found in the majority of patients with enlarged lymph nodes not attributed to AIDS, and at no risk for developing AIDS. Refer to @Aldhissla45’s tweet here. P Gluschankof et al, 1997 - This paper described in a video here with additional notes by Jamie here. Julian W. Bess Jr., 1997 - This paper described in a video here with additional notes by Jamie here. C.A. Cassol, 2020 - This paper is described by Andrew Kaufman here as well as by Thomas Cowan here. “Unofficially” we can also add the Lanka 3 phase control experiment that can be seen here or searched for it here. A further indication of the isolation procedure fallacy is shown in a study during which the CPE becomes more well defined with the addition of specific substances. The study is as follows: Leon Caly et al, 2020 - “Following several failures to recover virions with the characteristic fringes of surface spike proteins, it was found that adding trypsin to the cell culture medium immediately improved virion morphology.” See a video explanation here. Recent Requests and Statements Further and more recent requests and statements that were sent to me by my good friend Courtenay are as follows: May 5, 2022: U.S. CDC and Agency for Toxic Substances and Disease Registry confirmed that a search of their records failed to find any that describe anyone on Earth finding an alleged “avian influenza virus” in the bodily fluids of any diseased diseased host (animal or human) and purifying “it”… which is necessary so that “it” could be sequenced, characterized and studied with controlled experiments. This can be viewed here. May 20, 2022: Public Health Agency of Canada confirmed that they have no record of any alleged “avian influenza virus” having been found and purified from the bodily fluid/tissue/excrement of any diseased “host” on the planet (in order for “it” to be sequenced, characterized and studied with controlled experiments) by anyone, anywhere, ever. Insanely, they insist that: “Viruses” are in hosts despite their utter inability to find them there,. It’s necessary to “grow them” in non-host cells (as if “they” would grow better there than they allegedly grew in the diseased host lol). They pretend that mixing complex substances together results in purification. This can be viewed here. December 20, 2021: Public Health Agency of Canada confirmed that they have no record of any alleged “virus” having been purified from a sample taken from any diseased human on Earth, by anyone, ever, period. To be viewed here. March 11, 2022: U.S. Centers for Disease Control and Prevention and Agency for Toxic Substances and Disease Registry respond to a FOIA request for all studies / reports in their possession, custody or control describing the purification of any “virus” addressed by any “vaccine” on either their childhood or adult U.S. “immunization” schedule, directly from a sample taken from any diseased "host" on Earth where the sample was not first combined with any other source of genetic material. CDC/ATSDR provided 5 studies on “rotavirus” (thereby admitting they have no records for any other alleged viruses). None of these 5 studies actually describe isolation/purification of a “rotavirus” from a human. Request, response, studies to be viewed here. March 8, 2023: Italy 2020: Inside Covid’s “Ground zero” in Europe - Three years ago the Western World came to a standstill. The official Covid-19 narrative depicted a strange suddenly-super-spreading, deadlier-than-flu virus hailing from China that landed in Northern Italy. On February 20, 2020 the first alleged case of Covid-19 was discovered in the West in the Lombardy town of Codogno, Italy. Later that day the Italian government reported their first “Covid-19 death.” Dramatic media reports emerging from Northern Italy were hammered into and onto the Western psyche giving the impression there was a mysterious “super spreading” and “super lethal” novel virus galloping across the region infecting and killing scores of people. Read the rest of the report here. Conclusion The above list will be worked on over the coming years. If you think that any corrections need to be made or if you want to add additional studies, please leave a comment. Share Leave a comment https://open.substack.com/pub/dpl003/p/virology-the-damning-evidence?r=29hg4d&utm_medium=ios&utm_campaign=post
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    Virology - The Damning Evidence
    The Stake In The Heart For This Pseudoscientific Profession
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  • U.S. appeals court: FDA “overstepped” its authority with campaign to smear IVERMECTIN

    A federal appeals court has sided with three physicians who sued the Food and Drug Administration (FDA) over its campaign smearing the antiviral drug ivermectin.

    Charlie Kirk, founder of Turning Point USA (TPUSA), reported on the development in a post on X. He wrote: "The Fifth Circuit Court of Appeals in New Orleans has ruled in favor of three doctors allowing them to move forward with their lawsuit." According to Kirk, the bench argued that the FDA "abused its authority with anti-ivermectin messaging to Americans."

    "The FDA is not a physician. It has authority to inform, announce and apprise – but not to endorse, denounce or advise," Circuit Judge Don Willett ruled. "Left unmentioned in most of that messaging: Ivermectin also comes in a human version."

    "Remember: The FDA shamed Americans who used ivermectin off label," Kirk ultimately remarked. "The 'experts' failed you during the Wuhan coronavirus COVID-19 pandemic. Never again."

    Cardiologist Dr. Peter McCullough @P_McCulloughMD lauded the appeals court's decision in a post on X. He thanked the three plaintiffs – Drs. Mary Talley Bowden, Paul Marik and Robert Apter – for their "strength and courage." McCullough ultimately pointed out that "doctors decide the community standard of care," not the FDA or the Centers for Disease Control and Prevention.

    Rogan: Ivermectin smeared in order to secure EUA for vaccines

    Podcaster Joe Rogan of "The Joe Rogan Experience" also disclosed why the FDA was actively smearing ivermectin. According to him, the regulator did so in order to invoke the emergency use authorization (EUA) for the COVID-19 injections.

    "In order to utilize the EUA, they had to have no other remedies, no other effective treatment," Rogan told liberal actor and talk show host Bill Maher, who appeared on the podcast. "They didn't want any sort of way that you could get over this without taking their medicine."

    Kirk also shared a video of Sen. Ron Johnson @SenRonJohnsonUS (R-WI), an ardent defender of health freedom, with Maria Bartiromo of Fox News. The senator described the destruction caused by the actions of the FDA during his appearance on "Mornings with Maria."

    "The doctors I've been dealing with and talking to for years now, they believe that probably hundreds of thousands of Americans lost their lives because they were denied early treatment," Johnson said. "They were denied it because the FDA sabotaged … ivermectin."

    "They said: 'Come on, you all. You're not a cow, you're not a horse.' You know, this is supposedly horse medicine. No, this was a Nobel Prize-winning medicine that could have saved hundreds of thousands of lives."

    The TPUSA founder also thanked Johnson for his "leadership and bravery," and also accused the FDA of having "blood on its hands." Kirk continued: "How many Americans senselessly died because Big Medicine called this cheap, readily available Nobel Prize-winning medicine horse paste?"

    https://www.brighteon.com/aa04ea96-80ef-475b-ab79-b20b767cbdcf

    Join and share @NaturalNewsMedia
    U.S. appeals court: FDA “overstepped” its authority with campaign to smear IVERMECTIN A federal appeals court has sided with three physicians who sued the Food and Drug Administration (FDA) over its campaign smearing the antiviral drug ivermectin. Charlie Kirk, founder of Turning Point USA (TPUSA), reported on the development in a post on X. He wrote: "The Fifth Circuit Court of Appeals in New Orleans has ruled in favor of three doctors allowing them to move forward with their lawsuit." According to Kirk, the bench argued that the FDA "abused its authority with anti-ivermectin messaging to Americans." "The FDA is not a physician. It has authority to inform, announce and apprise – but not to endorse, denounce or advise," Circuit Judge Don Willett ruled. "Left unmentioned in most of that messaging: Ivermectin also comes in a human version." "Remember: The FDA shamed Americans who used ivermectin off label," Kirk ultimately remarked. "The 'experts' failed you during the Wuhan coronavirus COVID-19 pandemic. Never again." Cardiologist Dr. Peter McCullough @P_McCulloughMD lauded the appeals court's decision in a post on X. He thanked the three plaintiffs – Drs. Mary Talley Bowden, Paul Marik and Robert Apter – for their "strength and courage." McCullough ultimately pointed out that "doctors decide the community standard of care," not the FDA or the Centers for Disease Control and Prevention. Rogan: Ivermectin smeared in order to secure EUA for vaccines Podcaster Joe Rogan of "The Joe Rogan Experience" also disclosed why the FDA was actively smearing ivermectin. According to him, the regulator did so in order to invoke the emergency use authorization (EUA) for the COVID-19 injections. "In order to utilize the EUA, they had to have no other remedies, no other effective treatment," Rogan told liberal actor and talk show host Bill Maher, who appeared on the podcast. "They didn't want any sort of way that you could get over this without taking their medicine." Kirk also shared a video of Sen. Ron Johnson @SenRonJohnsonUS (R-WI), an ardent defender of health freedom, with Maria Bartiromo of Fox News. The senator described the destruction caused by the actions of the FDA during his appearance on "Mornings with Maria." "The doctors I've been dealing with and talking to for years now, they believe that probably hundreds of thousands of Americans lost their lives because they were denied early treatment," Johnson said. "They were denied it because the FDA sabotaged … ivermectin." "They said: 'Come on, you all. You're not a cow, you're not a horse.' You know, this is supposedly horse medicine. No, this was a Nobel Prize-winning medicine that could have saved hundreds of thousands of lives." The TPUSA founder also thanked Johnson for his "leadership and bravery," and also accused the FDA of having "blood on its hands." Kirk continued: "How many Americans senselessly died because Big Medicine called this cheap, readily available Nobel Prize-winning medicine horse paste?" https://www.brighteon.com/aa04ea96-80ef-475b-ab79-b20b767cbdcf Join and share 👉@NaturalNewsMedia
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  • 5 Reasons To Analyze Unknown Substance For Drugs, Poisons And Toxins

    In the fields of forensic science and public health, the analysis of unknown substances plays a pivotal role in ensuring the safety of individuals and communities. Unidentified materials may conceal potential threats in the form of drugs, poisons, or toxins. Read all about them in the blog.

    https://justpaste.it/analyze-unknown-substance
    5 Reasons To Analyze Unknown Substance For Drugs, Poisons And Toxins In the fields of forensic science and public health, the analysis of unknown substances plays a pivotal role in ensuring the safety of individuals and communities. Unidentified materials may conceal potential threats in the form of drugs, poisons, or toxins. Read all about them in the blog. https://justpaste.it/analyze-unknown-substance
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