• In San Jose, the heart of Silicon Valley, the pursuit of technological advancement goes hand in hand with a commitment to environmental stewardship and sustainability. Energy audits, a cornerstone of this eco-friendly initiative, represent a critical tool in San Jose’s effort to lead by example in energy conservation and sustainable living.
    In San Jose, the heart of Silicon Valley, the pursuit of technological advancement goes hand in hand with a commitment to environmental stewardship and sustainability. Energy audits, a cornerstone of this eco-friendly initiative, represent a critical tool in San Jose’s effort to lead by example in energy conservation and sustainable living.
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    Policy Impact on San Jose Energy Audits | VertPro®
    Uncover the impact of policy on energy audits in San Jose. Join the city's journey to sustainability through audits.
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  • Bird Flu Or H5N1 Vaccine Bioweapon?
    Dr. Ariyana Love (ND)

    Yesterday, CBS News reported that a case of the “bird flu” was identified in Texas. Federal agencies said the “virus had spread to dairy cattle across multiple states, including Texas”.

    What is “bird flu” exactly? They say it’s a “virus” that spreads from animals to humans but never in the history of medicine has an animal disease crossed species to infect humans.

    Bird flu is also known as the Avian Flu Virus, which is not actually a virus but the H5N1 bioweapon. I gave an interview with Stew Peters one year ago about how the NIH led by Anthony Fauci, enhanced the H1N1 pathogen through Gain-and-Loss-of-Function, from dead corpses in the 1918 “Spanish Flu” to produce the more lethal H5N1 bioweapon.

    Method for Producing the Flu Virus

    The method for producing the Avian Flu Virus which contains the H5N1 bioweapon, is patented and owned by Sanofi Pasteur, a French pharmaceutical company also headquartered in Israel, among other places. Read more here.


    There you have it, straight from the patent. In particular, H5N1 is used to increase mortality.

    Sanofi is the largest pharmaceutical company in the world that’s devoted entirely to vaccine inoculations. In 2020, Sanofi teamed up with GSK to provide the “S-protein” for Covid-19 vaccines.

    Sanofi will contribute its S-protein COVID-19 antigen, which is based on recombinant DNA technology. This technology has produced an exact genetic match to proteins found on the surface of the virus, and the DNA sequence encoding this antigen has been combined into the DNA of the baculovirus expression platform, the basis of Sanofi’s licensed recombinant influenza product in the US.

    A synthetic baculovirus bacteria that’s been genetically altered in a lab is Gain-of-Function. Read more about Sanofi’s “protein expression technologies” patent which is in other words a gene altering technology. Also review the “baculovirus vectors for cloning genes, and kits containing the baculovirus vectors” patent by Oxford.

    Indeed, the Bird Flu “vaccine” patent for chickens contains the H5N1 bioweapon.

    The Canadian Government incidentally has their own “Recombinant Avian Flu Vaccine” patent for chickens. The NIH National Cancer Institute’s definition of “recombinant” is this:

    “In genetics, describes DNA, proteins, cells, or organisms that are made by combining genetic material from two different sources. Recombinant substances are made in the laboratory and are being studied in the treatment of cancer and for many other uses.”

    WHO admits that patents were taken on the Avian Flu Virus. A paper by Nature from October 2023, reveals that CRISPR-Cas-9 is being used to alter the genome of chickens through inoculation, aka “vaccination”. The Canadian Government admits that it’s “highly pathogenic” and spreads between species. Natural pathogens can’t do this but bioweapons can.

    The NIH admits that the H5N1 spreads by “airborne transmission”. Virology Journal further affirms that the H5N1 is aerosolised. And another scientific study demonstrates that the H5N1 bioweapon is aerosolised after inoculation of chickens.

    Salon reported today that bird flu outbreaks are popping up across the United States. The article goes on to mention a “list of so-called zoonotic transmissions which includes Ebola, SARS-1, MERS, Lyme disease and most likely, SARS-CoV-2, the virus responsible for COVID-19”.

    Allow me to point out that Ebola is a patented bioweapon that’s used in COVID-19 vaccines. SARS-1 is a patented bioweapon owned by Chiron, a US based biotech company which is also used in COVID-19 vaccines. MERS is a patented bioweapon also owned by a US biotech company. Lyme Disease is from weaponized ticks, according to the U.S. Government’s own admittance.

    So, do you see a trend here? Do you see what they are doing? Chickens are being injected with bioweapons under the guise of “vaccination” to produce illness that spreads to other livestock and in some cases, humans. Although the “CDC considers the current risk to the general public from the H5N1 bird flu outbreak in wild birds and poultry to be low”, mainstream media is still pushing the false narrative that a “global bird flu pandemic in birds and other animals has been causing chaos for over three years now”.

    No, it’s just pharma and government poisoning our food supply to justify the culling of millions of chickens in the largest chicken egg manufacturers in America. Perhaps they want to starve us out just like their starving the Palestinians in besieged Gaza right now.

    Also read: The Covid-19 Vaccine Antigen is Anthrax

    https://substack.com/home/post/p-143213206
    Bird Flu Or H5N1 Vaccine Bioweapon? Dr. Ariyana Love (ND) Yesterday, CBS News reported that a case of the “bird flu” was identified in Texas. Federal agencies said the “virus had spread to dairy cattle across multiple states, including Texas”. What is “bird flu” exactly? They say it’s a “virus” that spreads from animals to humans but never in the history of medicine has an animal disease crossed species to infect humans. Bird flu is also known as the Avian Flu Virus, which is not actually a virus but the H5N1 bioweapon. I gave an interview with Stew Peters one year ago about how the NIH led by Anthony Fauci, enhanced the H1N1 pathogen through Gain-and-Loss-of-Function, from dead corpses in the 1918 “Spanish Flu” to produce the more lethal H5N1 bioweapon. Method for Producing the Flu Virus The method for producing the Avian Flu Virus which contains the H5N1 bioweapon, is patented and owned by Sanofi Pasteur, a French pharmaceutical company also headquartered in Israel, among other places. Read more here. There you have it, straight from the patent. In particular, H5N1 is used to increase mortality. Sanofi is the largest pharmaceutical company in the world that’s devoted entirely to vaccine inoculations. In 2020, Sanofi teamed up with GSK to provide the “S-protein” for Covid-19 vaccines. Sanofi will contribute its S-protein COVID-19 antigen, which is based on recombinant DNA technology. This technology has produced an exact genetic match to proteins found on the surface of the virus, and the DNA sequence encoding this antigen has been combined into the DNA of the baculovirus expression platform, the basis of Sanofi’s licensed recombinant influenza product in the US. A synthetic baculovirus bacteria that’s been genetically altered in a lab is Gain-of-Function. Read more about Sanofi’s “protein expression technologies” patent which is in other words a gene altering technology. Also review the “baculovirus vectors for cloning genes, and kits containing the baculovirus vectors” patent by Oxford. Indeed, the Bird Flu “vaccine” patent for chickens contains the H5N1 bioweapon. The Canadian Government incidentally has their own “Recombinant Avian Flu Vaccine” patent for chickens. The NIH National Cancer Institute’s definition of “recombinant” is this: “In genetics, describes DNA, proteins, cells, or organisms that are made by combining genetic material from two different sources. Recombinant substances are made in the laboratory and are being studied in the treatment of cancer and for many other uses.” WHO admits that patents were taken on the Avian Flu Virus. A paper by Nature from October 2023, reveals that CRISPR-Cas-9 is being used to alter the genome of chickens through inoculation, aka “vaccination”. The Canadian Government admits that it’s “highly pathogenic” and spreads between species. Natural pathogens can’t do this but bioweapons can. The NIH admits that the H5N1 spreads by “airborne transmission”. Virology Journal further affirms that the H5N1 is aerosolised. And another scientific study demonstrates that the H5N1 bioweapon is aerosolised after inoculation of chickens. Salon reported today that bird flu outbreaks are popping up across the United States. The article goes on to mention a “list of so-called zoonotic transmissions which includes Ebola, SARS-1, MERS, Lyme disease and most likely, SARS-CoV-2, the virus responsible for COVID-19”. Allow me to point out that Ebola is a patented bioweapon that’s used in COVID-19 vaccines. SARS-1 is a patented bioweapon owned by Chiron, a US based biotech company which is also used in COVID-19 vaccines. MERS is a patented bioweapon also owned by a US biotech company. Lyme Disease is from weaponized ticks, according to the U.S. Government’s own admittance. So, do you see a trend here? Do you see what they are doing? Chickens are being injected with bioweapons under the guise of “vaccination” to produce illness that spreads to other livestock and in some cases, humans. Although the “CDC considers the current risk to the general public from the H5N1 bird flu outbreak in wild birds and poultry to be low”, mainstream media is still pushing the false narrative that a “global bird flu pandemic in birds and other animals has been causing chaos for over three years now”. No, it’s just pharma and government poisoning our food supply to justify the culling of millions of chickens in the largest chicken egg manufacturers in America. Perhaps they want to starve us out just like their starving the Palestinians in besieged Gaza right now. Also read: The Covid-19 Vaccine Antigen is Anthrax https://substack.com/home/post/p-143213206
    SUBSTACK.COM
    Bird Flu Or H5N1 Vaccine Bioweapon?
    Yesterday, CBS News reported that a case of the “bird flu” was identified in Texas. Federal agencies said the “virus had spread to dairy cattle across multiple states, including Texas”. What is “bird flu” exactly? They say it’s a “virus” that spreads from animals to humans but never in the history of medicine has an animal disease crossed species to infect humans.
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  • Hey Steve Kirsch, Sars-Cov-2 is Still a Fraud and Your Genome Argument is a Disingenuous Sham
    The Health Freedom Movement's clown prince is at it again.

    Anthony Colpo

    Kirsch is back on the warpath. Humiliated after his admission that he relied entirely on the word of ‘experts’ as proof that Sars-Cov-2 had been isolated, he has now found salvation for himself and the rest of Team Pandemic.

    Or so he thinks.

    First, a little history.

    Kirsch insists Sars-Cov-2 is real, even though it has never been isolated by anything that even begins to resemble sound science.

    Kirsch has repeatedly refused to acknowledge the inherent absurdities in the viral ‘isolation’ charade. He has been informed repeatedly of these absurdities - but he flatly refuses to listen.

    More precisely, he doesn’t want to listen.

    Kirsch is Not a Very Clever Guy

    Kirsch likes to promote himself as a “pretty clever guy,” but he’s not.

    Kirsch advertised his scientific ineptitude back in January 2022 when he posted this terribly lame attempt at rebutting the no-virus argument.

    Kirsch’s post was titled “Has the virus been isolated? Yes.”

    Kirsch knows the virus has been isolated because … he doesn’t.

    Turns out Kirsch doesn’t have a clue about viral isolation. His knowledge of virology is as deficient as his stock-picking skills.

    Kirsch asked out aloud in his post:

    "Do these isolates have other stuff in them? How were they created?”

    The response?

    “I don’t know because I haven’t analyzed them personally. But my scientist friends seem happy with them."

    Thanks Steve. I love it when my dishonest critics reveal they have no clue what they’re talking about.

    "I rely on expert opinions of people who I trust for certain issues like whether or not the virus has been 'isolated.' It’s a reasonable approach if you are careful about which experts you trust."

    Among the ‘experts’ Kirsch ‘carefully’ trusts is the perennially angry, DARPA-funded, victim-narcissist Robert Malone, who apparently is such a genius that after observing how mRNA technology was still unfit for human use, allowed himself to be injected twice with it.

    Except that he didn’t, according to travelling partner Steven Hatfill.

    Yep, Kirsch sure knows how to pick his experts.

    Kirsch is Back on the Virus Warpath

    We all had a good laugh at Kirsch’s expense after his self-debunking “I rely on the experts” post.

    Kirsch, however, doesn’t like being laughed at. His ego demands that he be admired and revered as a really smart guy.

    So he got together with his ‘expert’ friends and plotted his rebuttal.

    Stevie Meets With His Masters

    “Steve,” said his ‘expert’ handler friend David Rockefelon III, “you’ll never win the no-virus argument by trying to claim the virus has been physically isolated - because it hasn’t.”

    “So what do I do?,” asked Kirsch.

    “In Davos, we have a saying,” chimed Rectal Swab. “If you can’t dazzle them with brilliance, baffle them with bullshit!”

    “I’m not sure I follow,” said a befuddled Kirsch.

    It was at this point that Gill Bates interjected. “Steve, you need to start posting articles about gene sequencing.”

    “Gene sequencing?” asked a perplexed Kirsch. “What’s that?”

    “Exactly,” replied Baron Badchild the 58th. “Most people don’t have a clue about genomics, so that’s where you need to steer the argument.”

    “You need to distract people from the fact that the virus has never been isolated. You are instead going to baffle them with the genome argument.”

    “How do I do that?” asked Kirsch.

    Badchild began his instructions. “You are going to post an article titled, 'How can millions of people, all exhibiting signs of COVID have whole genome sequences that match the SARS-CoV-2 reference genome if viruses don't exist?'"

    “I don’t even know what that means,” objected Kirsch.

    “You don’t need to know,” replied Swab. “Just post ze bloody article!”

    “But …”

    “But nothing!” roared the megalomaniac billionaires in unison.

    “Don’t forget its us who put you where you are now. And we can put you back down too," warned this Inhuman League of evil globalists.

    "But the four years we have had have been such good times, I still love you," replied a hurt Kirsch, on the verge of tears.

    “Stop being such a bloody sook!” Badchild threw a box of tissues at Kirsch. "Now get out there and do as you're told."

    And so Steve did as he was told. On June 14, 2024, he posted an article titled “How can millions of people, all exhibiting signs of COVID have whole genome sequences that match the SARS-CoV-2 reference genome if viruses don't exist?”

    The article, of course, made no mention that the alleged ‘genome’ of Sars-Cov-2 is a pseudoscientific farce.

    The article made no mention of the fact that the Sars-Cov-2 genome was not obtained by ‘deconstructing’ an actual virus, but created on a computer using the ‘sequencing’ ruse. Tiny, incomplete nucleotide sequences were fed into a computer, which was then allowed to create a 30,000-character genome. That’s like pulling off a tire, fanbelt and seat belt from a Volkswagen, feeding their details into a computer, and being told you have a Porsche.

    I’ll repeat it again, in case anyone doesn’t comprehend what I just wrote, because it is of critical importance:

    There is no such thing as a Sars-Cov-2 genome that was analyzed and documented after taking a Sars-Cov-2 virion and breaking it down into its constituent nucleotides.

    That has never been done, because Sars-Cov-2 has never been isolated. You can’t dismantle something that doesn’t exist.

    You can, however, take bits of something that does already exist, feed them into a computer, and allow it to construct an in silico ‘genome.’

    You set the parameters for both the in silico reconstruction and the accompanying PCR test to be sufficiently non-specific, so that millions of people exhibiting symptoms of cold and influenza and also millions of asymptomatic people exhibiting symptoms of nothing will miraculously have 'whole genome sequences' that match the 'Sars-CoV-2 reference genome.'

    Using ‘approved’ methods and test kits, of course.

    That’s why ‘Sars-Cov-2’ can be detected in fluid and blood samples taken from volunteers long before December 2019, which is when ‘Sars-Cov-2’ allegedly first appeared in the Chinese city of Wuhan.

    It explains why this supposedly ‘novel coronavirus’ was able to be detected in blood samples obtained in Mexico and Italy as far back as 2018, even though the official narrative has Sars-Cov-2 kicking off its World Domination Tour in early 2020.

    The non-specificity of the sequencing and testing charades also explains why it’s not just people with the sniffles and asymptomatic folks that miraculously show these 'whole genome sequences.' Papaya, quail and goat can also test positive for Sars-CoV-2!

    Heck, even sewerage floating through Catalonian caca pipes in March 2019 has tested positive for the Woohoo virus. "This striking finding," wrote the researchers who tested the Barcelona wastewater samples, "indicates circulation of the virus in Barcelona long before the report of any COVID-19 case worldwide."

    That’s because the nucleotide sequences that trigger a positive result for the presence of ‘Sars-Cov-2’ are not from a ‘novel virus’ - they are a common and preexisting phenomenon.

    Kirsch, of course, mentions none of this.

    His false bravado is in full swing when he again proposes another monetary challenge, this time a $10,000 bounty to anyone who can prove Sars-Cov-2 does not exist.


    NEWS FLASH: We don’t need to disprove the existence of a negative, Kirsch.

    If someone claims there are invisible goblins living under their kitchen table, no-one is obliged to prove them wrong. The onus is on the person issuing the unlikely claim to prove there are indeed invisible little people residing in their kitchen.

    Similarly, it’s up to those who claim the existence of a ‘novel’ and uber-deadly virus to prove its existence.

    So far, they’ve failed miserably.

    Taking gobs of phlegm from people with atypical pneumonia, mixing them with antibiotics, culture medium and bovine fetal serum is not isolation - its anti-isolation!

    Mixing this porqueria with African green monkey kidney cells - which can be relied upon to predictably deform in the presence of kidney-toxic antibiotics - is not proof that there is a pathogenic virus in the mix. It’s simply proof that virology has about as much credibility as witchcraft.

    Heck, the Doherty researchers who loudly proclaimed they isolated ‘Sars-Cov-2’ from the first Australian case admit in their paper the patient healed just fine with low-flow oxygen and antibiotics - which are for bacteria, not viruses!

    He was not suffering ‘COVID’, he was a pneumonia patient - no doubt one of many strategically flown around the world to help kick off the worldwide ‘isolation’ wank.

    I’ve already explained all this in detail here and here, so can I have my $10,000 now?

    Oh, wait, Steve Kirsch is a self-aggrandizing liar who has no intention of ever paying out on his challenges. Kirsch loves the rush of bravado and admiration he receives when he issues a bold challenge, but his “I’m a pretty clever guy” ruse makes no allowances for being wrong and publicly humiliated. That’s why he quickly goes into denial and cancel mode every time you fulfill one of his public challenges.

    The Real Challenge that Kirsch and the Scamdemic Crowd Need to Meet

    The real question is not “why millions of people, all exhibiting signs of COVID have whole genome sequences that match the SARS-CoV-2 reference genome if viruses don't exist?”

    The real questions that need asking are:

    Can anyone isolate Sars-Cov-2 in a manner that really does physically separate a pathogenic organism that can be subsequently shown to be an infectious and harmful virus?

    In other words, can this virus be shown to be transmittable between humans via coughing/sneezing/breathing/touching/’jumping”/etc etc etc and to cause the symptoms of ‘COVID’ upon infection?

    Upon having genuinely isolated this virus and proving it does cause an illness called ‘COVID’ in humans, can they then take virions from this virus and use those to catalog its entire genome?

    Can they then compare this genome to other similarly obtained ‘virus’ genomes from pre-December 2019 and point to key differences that prove the existence of a novel virus?

    No matter how Kirsch and his masters try to worm and squirm and reframe the argument, the inescapable truth is that the answer to all the above questions remains a big, fat NO.

    No-one has come close to doing this, and that includes the authors of this paper which Kirsch claims “the ‘no virus’ crowd stays clear of.”

    To cover for the inescapable fact that no-one has ever physically isolated a virus the way bacteria has been isolated, Kirsch gets his disingenuous on.

    “Fire can’t be isolated,” he says. “Gravity can’t be isolated.”

    Stupid Analogy Alert: Fire doesn’t need to be isolated the way a virus does. It can be seen with the naked eye, and there’s no mistaking it for a bunch of exosomes.

    As for gravity, of course you can’t “isolate” an invisible force. But I can sure as hell prove to you it exists, Kirsch, and in a manner in which it can’t be mistaken for anything else. Meet me at the top of a tall structure and I’ll explain.

    COVID: It’s Still Cold and Flu Renamed

    There is no Sars-Cov-2. There is no COVID.

    There is cold and flu and pneumonia, and they existed long before December 2019. In early 2020, they were renamed ‘COVID’ and the proof of its existence was testing positive on a fraudulent PCR test.

    That’s why, as the 'COVID' hysteria hit fever pitch during 2020, regular influenza magically disappeared almost entirely.

    Steve Kirsch, ladies and gentlemen, is part of the sham.

    I’ll have plenty more to say about Kirsch and the genome wank in due course, but today I’ll conclude with the following gems from our not-so-clever guy.

    “If the virus doesn’t exist, why is it we can SEE the SARS-CoV-2 under electron microscopes with its telltale ‘spikes’?” writes Kirsch.

    Excuse me Kirsch, but how do you know the alleged Sars-Cov-2 virions are not simply cellular vesicles - which is just what they look like?

    Go ahead, prove they’re actual virions from an infectious virus called Sars-Cov-2, using the methods outlined above.

    I’ll wait.

    Kirsch then proves just how utterly unsuited he is to this topic when he claims that a New York Times article from October 2020 “shows virions inside the cell as well as outside the cell.”

    “All of the images in the Times article are fully explained by virology,” claims Kirsch, “and are inexplicable if the virus doesn’t exist.”

    It’s time to have another hearty laugh at Stevie’s expense. Here are the images that the NYT reproduced, which any sober halfwit can tell are computer-generated creations:







    Pack it up and pack it in, Steve, this is getting beyond a joke.

    Share

    https://substack.com/home/post/p-146001238
    Hey Steve Kirsch, Sars-Cov-2 is Still a Fraud and Your Genome Argument is a Disingenuous Sham The Health Freedom Movement's clown prince is at it again. Anthony Colpo Kirsch is back on the warpath. Humiliated after his admission that he relied entirely on the word of ‘experts’ as proof that Sars-Cov-2 had been isolated, he has now found salvation for himself and the rest of Team Pandemic. Or so he thinks. First, a little history. Kirsch insists Sars-Cov-2 is real, even though it has never been isolated by anything that even begins to resemble sound science. Kirsch has repeatedly refused to acknowledge the inherent absurdities in the viral ‘isolation’ charade. He has been informed repeatedly of these absurdities - but he flatly refuses to listen. More precisely, he doesn’t want to listen. Kirsch is Not a Very Clever Guy Kirsch likes to promote himself as a “pretty clever guy,” but he’s not. Kirsch advertised his scientific ineptitude back in January 2022 when he posted this terribly lame attempt at rebutting the no-virus argument. Kirsch’s post was titled “Has the virus been isolated? Yes.” Kirsch knows the virus has been isolated because … he doesn’t. Turns out Kirsch doesn’t have a clue about viral isolation. His knowledge of virology is as deficient as his stock-picking skills. Kirsch asked out aloud in his post: "Do these isolates have other stuff in them? How were they created?” The response? “I don’t know because I haven’t analyzed them personally. But my scientist friends seem happy with them." Thanks Steve. I love it when my dishonest critics reveal they have no clue what they’re talking about. "I rely on expert opinions of people who I trust for certain issues like whether or not the virus has been 'isolated.' It’s a reasonable approach if you are careful about which experts you trust." Among the ‘experts’ Kirsch ‘carefully’ trusts is the perennially angry, DARPA-funded, victim-narcissist Robert Malone, who apparently is such a genius that after observing how mRNA technology was still unfit for human use, allowed himself to be injected twice with it. Except that he didn’t, according to travelling partner Steven Hatfill. Yep, Kirsch sure knows how to pick his experts. Kirsch is Back on the Virus Warpath We all had a good laugh at Kirsch’s expense after his self-debunking “I rely on the experts” post. Kirsch, however, doesn’t like being laughed at. His ego demands that he be admired and revered as a really smart guy. So he got together with his ‘expert’ friends and plotted his rebuttal. Stevie Meets With His Masters “Steve,” said his ‘expert’ handler friend David Rockefelon III, “you’ll never win the no-virus argument by trying to claim the virus has been physically isolated - because it hasn’t.” “So what do I do?,” asked Kirsch. “In Davos, we have a saying,” chimed Rectal Swab. “If you can’t dazzle them with brilliance, baffle them with bullshit!” “I’m not sure I follow,” said a befuddled Kirsch. It was at this point that Gill Bates interjected. “Steve, you need to start posting articles about gene sequencing.” “Gene sequencing?” asked a perplexed Kirsch. “What’s that?” “Exactly,” replied Baron Badchild the 58th. “Most people don’t have a clue about genomics, so that’s where you need to steer the argument.” “You need to distract people from the fact that the virus has never been isolated. You are instead going to baffle them with the genome argument.” “How do I do that?” asked Kirsch. Badchild began his instructions. “You are going to post an article titled, 'How can millions of people, all exhibiting signs of COVID have whole genome sequences that match the SARS-CoV-2 reference genome if viruses don't exist?'" “I don’t even know what that means,” objected Kirsch. “You don’t need to know,” replied Swab. “Just post ze bloody article!” “But …” “But nothing!” roared the megalomaniac billionaires in unison. “Don’t forget its us who put you where you are now. And we can put you back down too," warned this Inhuman League of evil globalists. "But the four years we have had have been such good times, I still love you," replied a hurt Kirsch, on the verge of tears. “Stop being such a bloody sook!” Badchild threw a box of tissues at Kirsch. "Now get out there and do as you're told." And so Steve did as he was told. On June 14, 2024, he posted an article titled “How can millions of people, all exhibiting signs of COVID have whole genome sequences that match the SARS-CoV-2 reference genome if viruses don't exist?” The article, of course, made no mention that the alleged ‘genome’ of Sars-Cov-2 is a pseudoscientific farce. The article made no mention of the fact that the Sars-Cov-2 genome was not obtained by ‘deconstructing’ an actual virus, but created on a computer using the ‘sequencing’ ruse. Tiny, incomplete nucleotide sequences were fed into a computer, which was then allowed to create a 30,000-character genome. That’s like pulling off a tire, fanbelt and seat belt from a Volkswagen, feeding their details into a computer, and being told you have a Porsche. I’ll repeat it again, in case anyone doesn’t comprehend what I just wrote, because it is of critical importance: There is no such thing as a Sars-Cov-2 genome that was analyzed and documented after taking a Sars-Cov-2 virion and breaking it down into its constituent nucleotides. That has never been done, because Sars-Cov-2 has never been isolated. You can’t dismantle something that doesn’t exist. You can, however, take bits of something that does already exist, feed them into a computer, and allow it to construct an in silico ‘genome.’ You set the parameters for both the in silico reconstruction and the accompanying PCR test to be sufficiently non-specific, so that millions of people exhibiting symptoms of cold and influenza and also millions of asymptomatic people exhibiting symptoms of nothing will miraculously have 'whole genome sequences' that match the 'Sars-CoV-2 reference genome.' Using ‘approved’ methods and test kits, of course. That’s why ‘Sars-Cov-2’ can be detected in fluid and blood samples taken from volunteers long before December 2019, which is when ‘Sars-Cov-2’ allegedly first appeared in the Chinese city of Wuhan. It explains why this supposedly ‘novel coronavirus’ was able to be detected in blood samples obtained in Mexico and Italy as far back as 2018, even though the official narrative has Sars-Cov-2 kicking off its World Domination Tour in early 2020. The non-specificity of the sequencing and testing charades also explains why it’s not just people with the sniffles and asymptomatic folks that miraculously show these 'whole genome sequences.' Papaya, quail and goat can also test positive for Sars-CoV-2! Heck, even sewerage floating through Catalonian caca pipes in March 2019 has tested positive for the Woohoo virus. "This striking finding," wrote the researchers who tested the Barcelona wastewater samples, "indicates circulation of the virus in Barcelona long before the report of any COVID-19 case worldwide." That’s because the nucleotide sequences that trigger a positive result for the presence of ‘Sars-Cov-2’ are not from a ‘novel virus’ - they are a common and preexisting phenomenon. Kirsch, of course, mentions none of this. His false bravado is in full swing when he again proposes another monetary challenge, this time a $10,000 bounty to anyone who can prove Sars-Cov-2 does not exist. NEWS FLASH: We don’t need to disprove the existence of a negative, Kirsch. If someone claims there are invisible goblins living under their kitchen table, no-one is obliged to prove them wrong. The onus is on the person issuing the unlikely claim to prove there are indeed invisible little people residing in their kitchen. Similarly, it’s up to those who claim the existence of a ‘novel’ and uber-deadly virus to prove its existence. So far, they’ve failed miserably. Taking gobs of phlegm from people with atypical pneumonia, mixing them with antibiotics, culture medium and bovine fetal serum is not isolation - its anti-isolation! Mixing this porqueria with African green monkey kidney cells - which can be relied upon to predictably deform in the presence of kidney-toxic antibiotics - is not proof that there is a pathogenic virus in the mix. It’s simply proof that virology has about as much credibility as witchcraft. Heck, the Doherty researchers who loudly proclaimed they isolated ‘Sars-Cov-2’ from the first Australian case admit in their paper the patient healed just fine with low-flow oxygen and antibiotics - which are for bacteria, not viruses! He was not suffering ‘COVID’, he was a pneumonia patient - no doubt one of many strategically flown around the world to help kick off the worldwide ‘isolation’ wank. I’ve already explained all this in detail here and here, so can I have my $10,000 now? Oh, wait, Steve Kirsch is a self-aggrandizing liar who has no intention of ever paying out on his challenges. Kirsch loves the rush of bravado and admiration he receives when he issues a bold challenge, but his “I’m a pretty clever guy” ruse makes no allowances for being wrong and publicly humiliated. That’s why he quickly goes into denial and cancel mode every time you fulfill one of his public challenges. The Real Challenge that Kirsch and the Scamdemic Crowd Need to Meet The real question is not “why millions of people, all exhibiting signs of COVID have whole genome sequences that match the SARS-CoV-2 reference genome if viruses don't exist?” The real questions that need asking are: Can anyone isolate Sars-Cov-2 in a manner that really does physically separate a pathogenic organism that can be subsequently shown to be an infectious and harmful virus? In other words, can this virus be shown to be transmittable between humans via coughing/sneezing/breathing/touching/’jumping”/etc etc etc and to cause the symptoms of ‘COVID’ upon infection? Upon having genuinely isolated this virus and proving it does cause an illness called ‘COVID’ in humans, can they then take virions from this virus and use those to catalog its entire genome? Can they then compare this genome to other similarly obtained ‘virus’ genomes from pre-December 2019 and point to key differences that prove the existence of a novel virus? No matter how Kirsch and his masters try to worm and squirm and reframe the argument, the inescapable truth is that the answer to all the above questions remains a big, fat NO. No-one has come close to doing this, and that includes the authors of this paper which Kirsch claims “the ‘no virus’ crowd stays clear of.” To cover for the inescapable fact that no-one has ever physically isolated a virus the way bacteria has been isolated, Kirsch gets his disingenuous on. “Fire can’t be isolated,” he says. “Gravity can’t be isolated.” Stupid Analogy Alert: Fire doesn’t need to be isolated the way a virus does. It can be seen with the naked eye, and there’s no mistaking it for a bunch of exosomes. As for gravity, of course you can’t “isolate” an invisible force. But I can sure as hell prove to you it exists, Kirsch, and in a manner in which it can’t be mistaken for anything else. Meet me at the top of a tall structure and I’ll explain. COVID: It’s Still Cold and Flu Renamed There is no Sars-Cov-2. There is no COVID. There is cold and flu and pneumonia, and they existed long before December 2019. In early 2020, they were renamed ‘COVID’ and the proof of its existence was testing positive on a fraudulent PCR test. That’s why, as the 'COVID' hysteria hit fever pitch during 2020, regular influenza magically disappeared almost entirely. Steve Kirsch, ladies and gentlemen, is part of the sham. I’ll have plenty more to say about Kirsch and the genome wank in due course, but today I’ll conclude with the following gems from our not-so-clever guy. “If the virus doesn’t exist, why is it we can SEE the SARS-CoV-2 under electron microscopes with its telltale ‘spikes’?” writes Kirsch. Excuse me Kirsch, but how do you know the alleged Sars-Cov-2 virions are not simply cellular vesicles - which is just what they look like? Go ahead, prove they’re actual virions from an infectious virus called Sars-Cov-2, using the methods outlined above. I’ll wait. Kirsch then proves just how utterly unsuited he is to this topic when he claims that a New York Times article from October 2020 “shows virions inside the cell as well as outside the cell.” “All of the images in the Times article are fully explained by virology,” claims Kirsch, “and are inexplicable if the virus doesn’t exist.” It’s time to have another hearty laugh at Stevie’s expense. Here are the images that the NYT reproduced, which any sober halfwit can tell are computer-generated creations: Pack it up and pack it in, Steve, this is getting beyond a joke. Share https://substack.com/home/post/p-146001238
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  • Why the Official AIDS Story is a Complete Crock
    The Great Rebranding, 1980s-Style: HIV Was a Sham, Just Like Sars-Cov-2

    Anthony Colpo

    All you youngsters born after the Glomesh era have surely heard of AIDS, but probably have no idea of just how big a deal it was when it burst onto the scene in the early 1980s.

    It was the biggest show in town. Sure, it wasn't as big a deal as what COVID would later be. It wasn't accompanied by 'vaccine' mandates, lockdowns or heavily-armed goons bashing people for sitting peacefully in the park. Instead of masks, there were condoms and paper toilet seat covers. There was no social distancing, only admonitions to avoid unprotected sex and not share needles when shooting up.

    Fauci was there, front and center, but he wasn't telling us to wear two condoms at once. Instead, he was pimping a toxic concoction known as AZT.

    Right off the bat, nothing made sense about the AIDs charade. It does make sense in hindsight if you view it as a giant test run, an exercise in spreading 'virus' hysteria. The HIV/AIDS charade confirmed most people don't ask questions, and those who do can be quickly shouted over and marginalized as "deniers," "conspiracists" and menaces to society. It also confirmed that not only could people be convinced to take toxic drugs in response to an overblown 'pandemic' scare, but they could be manipulated into rabidly demanding their expedited release.

    It was an exercise whose lessons would prove valuable come December 2019.

    AIDS stands for "acquired immunodeficiency syndrome." In other words, you somehow "acquired" an immune system that, like a tired car engine with 300,000 km on the clock, was about to blow its last gasket.

    It was first identified in 1981 in Los Angeles when the CDC reported on five young homosexual men suffering pneumonia caused by a protozoon known as Pneumocystis carinii.

    This microbe is ordinarily innocuous and, in fact, found in nearly all healthy persons. For reasons unknown it had suddenly become lethal - an outcome previously seen only in persons whose immune systems were being undermined by immunosuppressant therapy, cancer, or severe malnourishment.

    This same pneumonia promptly appeared in New York, together with several dozen cases of an unusual skin cancer called Kaposi's Sarcoma which had previously been almost unknown in the US.

    Eventually Pneumocystis carinii pneumonia and Kaposi's Sarcoma were interpreted as secondary manifestations of an underlying immune-system deficiency of unknown origin which was eventually dubbed "acquired immunodeficiency disease syndrome" or AIDS.

    The bodies of AIDS patients seemed to have just given up. Patients suffered severe weight loss and lethargy and were so immune deficient that even a minor infection threatened to kill them.

    The first few thousand cases were found mostly in homosexual males, and the media bombarded us with images of emaciated gay blokes on the verge of death and barely able to sit upright. Initially, the condition was referred to as GRID (gay-related immune deficiency). Outside of scientific circles, it came to be known as the "gay plague" and religious fundamentalists trumpeted the phenomenon as God's revenge on evil sodomites.

    That began to change in 1983, when AIDS was found to affect heterosexual women, which caused the fear porn to increase by an order of magnitude. As with COVID, health authorities treated us to an orgy of fearmongering and doomsday predictions - and the sheeple lapped it up.

    In 1986, Dr. Donald Ian Macdonald, then Acting Assistant Secretary of Health and Human Services, described "the escalating AIDS epidemic" as "staggering," "devastating" and a "huge problem."

    Dr. Halfdan Mahler, Danish physician and head of the World Health Organization, called AIDS "a health disaster of pandemic proportions" and said he could "not imagine a worse health problem in this century."

    "We stand nakedly in front of a very serious pandemic as mortal as any pandemic there ever has been," Mahler bizarrely quipped. Why he would don his birthday suit instead of a Hazmat one in the face of such a mortal pandemic was never explained, but that's globalist bureaucrats for you.

    "I don't know of any greater killer than AIDS, not to speak of its psychological, social and economic maiming," continued Mahler, who after leaving WHO became director of the International Planned Parenthood Federation.

    Not to be outdone, in 1987 Harvard biology professor Stephen Jay Gould, said AIDS was "potentially, the greatest natural tragedy in human history." He warned "AIDS may run through the entire population, and may carry off a quarter or more of us" (in 1987, the world population was just over 5 billion; it now stands at over 8 billion).

    That same year, Gallup asked an open-ended question about what Americans saw as the most urgent health problem facing the US. Despite the fact AIDS has never even come close to being the leading cause of death in the US, more than two-thirds of Americans said AIDS. The disease continued as the top pick until 2000.

    According to Gallop polls conducted in 1987, most Americans (60%) agreed people with AIDS should be made to carry a card noting they had the disease, and one in three (33%) agreed employers should be allowed to fire employees who had AIDS. Twenty-one percent of Americans said people with AIDS should be isolated from the rest of society.

    An earlier LA Times poll from 1985 found more than half of US adults supported quarantining AIDS patients, nearly half would approve of ID cards for those testing positive for "AIDS antibodies," and one in seven favored tattooing those with the disease.

    People never learn.

    A Disease Looking For a Cause

    Authorities had presented us with a new public health scare, but no causal agent. No-one knew what caused the immune systems of AIDS patients to become so deficient.

    Was it a new microbe? A new drug scourge? God's revenge for Abba and Disco Duck?

    No-one knew.

    At least officially.

    In reality, authorities knew damn well what was going on.

    But they didn’t tell us. Instead, they eventually claimed AIDS was the result of a 'novel virus' that, in 1986, was named "human immunodeficiency virus,” or HIV.

    The 'novel virus' paradigm holds that a 'zoonotic' virus wakes up one day, and decides to "jump" from apes/bats/pangolins/garden gnomes to humans. This novel virus then acts like a seventeen year old that has been given the keys to an alcohol-filled mansion while mom and dad head off for a weekend vacation. However, the virus has no friends to party with. So he first has to convert to a 'human' form of the virus, then he has to begin self-replicating in order to build a social circle. Once this is done, the virions party so hard that the host becomes sick. The virions conclude their current host is no fun, so they go looking for a new host to party inside. The process repeats itself, and before you know it, there's a 'pandemic' going on with squillions of little virions pogo-dancing in global synchrony and chanting "the roof, the roof, the roof is on fire!!" while trashing everything in sight.

    Viruses these days, sheesh.

    Setting aside the glaring fallacies of the virus 'isolation' charade, the 'novel virus = pandemic’ theory is an inherent load of cobblers.

    Outbreaks of what look to be infectious illnesses don't just happen for no reason. There has to be some facilitating factor.

    AIDS became a big thing in the early 1980s, and we know that initially, the majority of patients were gay males. African-Americans were also known to be at increased risk.

    Even if butt sex is an especially efficient method of transmitting STDs, it doesn't explain why AIDS became a phenomenon in the 1980s. After all, both sodomy and homosexuality have been around as long as humans have. Heck, even apes have been observed taking rides on the Hershey Highway.

    Which begs the question: What other events with the potential for dire impact on health occurred around the same time as the AIDS outbreak?

    The Other Crack Rears Its Ugly Head

    Thanks in no small part to Uncle Sam and his ability to conveniently look the other way when it suits his financial and geopolitical interests*, the early 1980s saw a massive flood of cocaine into the US, with urban black neighborhoods the worst afflicted.

    So plentiful was the supply of cocaine, drug dealers came up with a way to make it even cheaper and more addictive in order to expand their customer base.

    Freebase is the name given to the original form of smokable coke, which resulted in a more intense high than snorting. While this constituted an obvious selling point, the process for making freebase required ether, making it notoriously volatile and dangerous to produce. In a famed 1980 incident, comedian Richard Pryor suffered severe and life-threatening burns after mixing cocaine with ether at his home; the mixture promptly exploded in his face.

    Freebase cocaine seems to have first surfaced in the US in the mid-1970s. Around 1980, a less volatile but similar process was developed by dealers in which cocaine was dissolved in a solution of water and baking soda and then dried out into "crack rocks." As the rocks are heated, it makes a crackling sound, hence the name.

    As early as 1981, reports of crack appeared in Los Angeles, San Diego, Houston, and in the Caribbean. Its use quickly spread to other major US cities, and by 1987, crack was reportedly available in DC and all but four states in the Union.

    "In some major cities, such as New York, Detroit, and Philadelphia, one dosage unit of crack could be obtained for as little as $2.50," writes the US DEA. "Never before had any form of cocaine been available at such low prices and at such high purity."

    The crack epidemic dramatically increased the number of Americans addicted to cocaine, as well as the number of cocaine-related hospital emergencies. In 1985, cocaine-related hospital emergencies rose by 12 percent, from 23,500 to 26,300. In 1986, these incidents increased 110 percent, from 26,300 to 55,200.

    The crack cocaine explosion, you'll notice, overlaps neatly with the AIDS "explosion."

    The House of Representatives Select Committee on Narcotics Abuse and Control held cocaine hearings in July, October, and November 1980. Dr. Robert Byck, who along with his colleagues conducted the first scientific studies of cocaine plasma levels after coca paste smoking, testified at the hearings. He warned that the heavy use of smokable freebase cocaine, employed by an estimated 10 percent of cocaine users, was about to change. He warned Congress that the US was about to experience the worst epidemic of drug abuse the country had ever seen. Byck predicted the use of smoked cocaine in the 1980s would match the widespread use of "speed" (methamphetamine) in the 1960s. He urged Congress and the National Institute on Drug Abuse to mount an education and prevention campaign to avert this impending epidemic.

    No such campaign was undertaken.

    "The emergence of crack cocaine use in the United States during the mid-1980s was one of the most significant public health problems of that era," note Watkins et al in a 1998 paper. "Crack use contributed to a series of sexually transmitted disease epidemics, to epidemic increases in violent injuries and homicides, and to significant increases in the incidence and prevalence of cocaine addiction. Despite these threats to health and safety, a national public health campaign to counter crack-related morbidity and mortality was never mounted."

    Is that because authorities were already committed to carrying out a manufactured 'HIV' crisis?

    Crack, Risky Sex, and 'HIV'

    A 1994 NEJM article reported an analysis of 1,967 people recruited from inner-city neighborhoods in New York, Miami, and San Francisco. All respondents reported never having injected drugs, however 1,137 were regular smokers of crack. The remaining 830 people reported never having smoked crack.

    The results for crack users weren't pretty.

    Female crack users were 4.1 times more likely to have been raped, and 1.6 times more likely to have had their first vaginal or anal sex encounter before 13 years of age.

    Both male and female crack users reported a higher number of sexual partners than non-users; in the case of women, crack users were 11 times more likely to have had 50 or more sexual partners.

    Crack-smoking women were 13.5 times more likely than nonsmoking women to have engaged in sexual work at any time, and 28.8 times more likely to have engaged in recent, unprotected sex work.

    Male crack smokers, meanwhile, were 3.4 times more likely to report ever having homosexual anal sex, and 23 times more likely to have had 50 or more male anal sex partners.

    Clearly, crack users were significantly more likely to engage in prostitution and risky sexual practices.

    Not surprising then, that female and male crack users had higher historical rates of syphilis (3.5 and 2.2, respectively) and gonorrhea (1.8 and 1.6, respectively).

    When the researchers ran blood tests for current infection, female and male crack users were significantly more likely to test positive for syphilis (2.8 and 1.6, respectively).

    Among the participants in New York and Miami, HIV 'infection' was 2.3 times more prevalent among crack smokers than among nonsmokers (prevalence of HIV antibodies among participants recruited in San Francisco was low).

    Testing positive for ‘HIV antibodies’ was strongly associated with previous or current infection with other STDs.

    A positive reactive syphilis test (adjusted odds ratio, 2.3) and a history of herpes (adjusted odds ratio, 3.6) remained significantly associated with HIV infection after adjustment for high-risk sexual practices and African-American race.

    Other studies found similar results.

    Chiasson and colleagues at the New York City Department of Health examined the link between HIV infection and crack use. Examining patients at an STD clinic in the South Bronx, they found that, among women with no other identified risk (i.e., no injectible drug use), crack use, prostitution, crack-using prostitution and history of syphilis were all found to be risk factors for HIV infection. Among men with no other risk behavior, a history of syphilis was in fact the strongest predictor of HIV infection - greater than crack use and contact with prostitutes.

    In a 1990 paper, Greenspan and Castro note "between 1981 and 1983, the incidence of primary and secondary syphilis in the United States increased 34%, reaching a rate in 1989 (18.4 cases per 100,000 persons) that was higher than at any time since 1949. Between 1985 and 1989, incidence among blacks more than doubled, from 52.5 to 121.8 cases per 100,000; the increase was greater for black women than for black men (176% versus 106%). These trends are markers for the same high-risk sexual practices that promote transmission of HIV."

    So crack, syphilis and ‘HIV’ are closely related. Now let's look at another class of drugs showing a close correlation with pre-existing STDs and ‘HIV.’

    The Popper Phenomenon

    “Poppers” is a slang term for nitrite inhalant drugs (when they were first manufactured, they came in small ampoules that were 'popped' to release fumes). Amyl nitrite was originally developed to treat angina pectoris by dilating blood vessels, allowing the heart to get more oxygen and thereby relieving the pain.

    Arteries are not the only thing poppers help to dilate. Inhaling nitrites relaxes smooth muscles throughout the body - including the sphincter muscles, making it particularly helpful to gay posteriors. Along with facilitating anal sex, the blood vessel-dilating effects of poppers can produce a brief but intense sensation of heat and euphoria lasting 1 or 2 minutes.

    The story of poppers is an interesting one, involving US Vietnam vets, a profiteering Big Pharma and an enabling FDA, a gay medical student and organized criminals.

    The latter two entities sidestepped an eventual prescription requirement for amyl nitrite by creating butyl and isobutyl nitrite - less pure, more toxic, and even faster-acting versions than the original. Further restrictions were averted thanks to an unwritten agreement between producers and the FDA that poppers were only to be advertised in gay-oriented publications, as 'room deodorizers.'

    During the 1970s and early 80s, poppers were advertised heavily in the gay press, and the drugs became an integral part of gay culture. Not only was it routine for patrons at gay nightclubs to freely pass the vials around, some "disco clubs would even add to the general euphoria by occasionally spraying the dance floor with poppers fumes."

    "The miasma of nitrite fumes was taken for granted at gay gathering places: bars, baths, leather clubs," writes John Lauritsen in a 1994 New York Native article. "Some gay men were never without their little bottle, from which they snorted fumes around the clock."

    Throwing caution to the wind when it comes to drugs never ends well. Amyl nitrite was developed for occasional use by angina patients, not as a party drug to be snorted every time one hit the dance floor or engaged in a bout of Jolly Rogering.

    Apart from causing localized damage to nasal membranes, poppers have been linked to anemia, strokes, heart, lung, and brain damage, cardiovascular collapse, and, tellingly, the blood de-oxygenation, thymus atrophy, chronic depletion of T-cell ratio's associated with severe immune dysfunction. The drugs have also been linked to the development of Kaposi's Sarcoma.

    Sounds a lot like AIDS, doesn't it?

    While researchers and the more level-headed of gay advocates warned of the dangers, the FDA continued to look the other way. The gay press, whose advertising revenue relied heavily on popper ads, also willfully turned a blind eye to the dangers.

    In the 1980s, in a lukewarm attempt to be seen to be doing something about the problem, US health officials banned the use of poppers in public places and required merchants to post warnings about their dangers. "The warnings about their use disappeared sometime in the late '80s to early '90s," reports SFGATE, "and no one seems to know why."

    "During the first few years of the AIDS epidemic," writes Ian Young at VirusMyth.org, "poppers came under suspicion as a possible contributing factor. But after 1984, when the Reagan administration pronounced a single retrovirus to be the only cause of the growing list of AIDS illnesses, the health hazards of poppers were dismissed. All attention and funding was directed to HIV."

    Fun fact: Burroughs Wellcome, the original manufacturers of poppers, went on to profit handsomely from the subsequent AIDS hysteria with its highly-toxic 'anti-AIDS' drug AZT.

    History is Made (Up)

    There were major drug scourges afflicting the high-risk gay and African-American communities, drugs whose chronologies overlapped neatly with the AIDS outbreak. Use and abuse of these drugs was well established to cause severe illness, immune dysfunction and was also strongly correlated with pre-existing STDs like syphilis.

    The powers-that-be, however, had already decided the sole cause of AIDs was a 'novel virus.' They just needed to come up with one.

    And so along came the virologists to save the day. Not just any old bunch of virologists, but virologists with friends in high places. In France, this meant Luc Montagnier and his team at the Pasteur Institute, which advises the French government and the World Health Organization (WHO), and maintains a close collaboration with the US Centers for Disease Control and Prevention (CDC).

    In the US, it meant sci-bureaucrats from the government's behemoth National Institutes of Health (NIH). One of the key figures was the caustic Robert S Gallo, a researcher at the NIH's National Cancer Institute, where he worked for 30 years mainly as head of the Laboratory of Tumor Cell Biology. Gallo’s career would be dogged by controversy and misconduct allegations, but that’s a whole other article (stay tuned).

    The other career bureaucrat that would play a key role on the US side was none other than Anthony S Fauci, who recently completed a ridiculous 38-year reign as unelected head of the NIH's National Institute of Allergy and Infectious Diseases (NIAID).

    If you've surmised that, with names like the above, the HIV story must be a real shite show, you are absolutely correct.

    HIV is Invented 'Discovered'

    In 1983, the Pasteur Institute researchers declared they had 'isolated' a 'retrovirus' belonging to the family of T-cell leukemia viruses (HTLV), and concluded it "may be involved in several pathological syndromes, including AIDS." (Bold emphasis added)

    Their isolate came from a promiscuous 33-year-old Caucasian homosexual male referred to as "BRU", who indicated he'd had more than 50 sexual partners per year. Nasty. According to the authors, he displayed "signs and symptoms that often precede the acquired immune deficiency syndrome (AIDS)." However, the only symptoms reported for the patient were multiple lymphadenopathies (swollen lymph glands) and asthenia (weakness), which are evident in many conditions aside from AIDS. Neither fever nor recent loss of weight were noted.

    In other words, the patient from whom the alleged AIDS-causing virus was first 'isolated' from did not have an AIDS diagnosis.

    Tellingly, the patient did have a history of several episodes of gonorrhea and had been treated for syphilis in September 1982. Lymphadenopathy is one of the symptoms of both the aforementioned infections.

    The study's lead author was Francoise Barre-Sinoussi, although the finding is routinely credited to the paper's last listed author, the late Montagnier.

    The French study was marred by two key problems. It did not isolate any virus, and it did not show AIDS was caused by any HTLV offshoot.

    Forty years later, little has changed. The terminology and rationalizations have indeed become increasingly complex (as is the case with most elaborate lies), but there is no physical isolate of 'HIV.'

    Virologists and their sycophants, of course, insist this doesn't matter and that their non-purified mixtures are indeed isolates.

    While they condescendingly sneer and dismiss anyone who disputes this as a silly little dumb-dumb that doesn't 'understand' virology, they tend to remain rather quiet on another highly inconvenient observation.

    Namely, there is no proof that whatever is in their ‘isolates’ actually causes AIDS.

    HIV and Sars-Cov-2: The 'Deadly' Viruses That Aren't Deadly

    In the early days of 'COVID', testing positive for the mythical Sars-Cov-2 was considered a death sentence. So much so, that some folks didn't even bother getting their affairs in order; they instead killed themselves.

    Such is the power of all this heinous "deadly virus" bullshit.

    It was the same in the 'HIV' Dark Ages - testing positive was considered a death sentence. When a famous basketballer by the name of Erving “Magic” Johnson announced he was HIV positive in 1991, everyone was shocked. "Now we all know someone with HIV," said someone I can't recall in what was supposed to be a profound, insight-triggering moment.

    Johnson, everyone assumed, was now living on borrowed time.

    Thirty-three years later, Johnson is still alive and wealthy. He attributes his survival to antiretroviral cocktails that have never been shown in clinical studies to benefit survival: GlaxoSmithKline's Trizivir and Abbott's Kaletra. These cocktails are comprised of drugs like AZT which increase the risk of side effects but have never been shown to exert a mortality benefit.

    Johnson, it should be noted, has featured in ads for both products. In 2009, the FDA issued a warning letter to Abbott Laboratories regarding a promotional DVD in which Johnson discussed his experiences with Kaletra. The letter stated the violations were of public health concern "because they suggest that Kaletra is safer and more effective than has been demonstrated by substantial evidence or substantial clinical experience, and encourage use in circumstances other than those for which the drug has been shown to be safe and effective."

    "FDA is not aware of substantial evidence or substantial clinical experience to support effectiveness for five or more years of treatment with Kaletra in treatment-experienced adults. The personal experience of Kaletra patients, such as Magic Johnson, does not constitute such evidence."

    So if overpriced drug cocktails aren't keeping Johnson alive, what explains his survival?

    It's explained by the fact that HIV is a load of bollocks. A shady test that claims you are ‘HIV positive’ does not mean you are in fact harboring a deadly 'virus.'

    If ‘HIV’ was so deadly, then lab animals infected with it would get sick and die.

    But guess what? Administering a so-called isolate of uber-deadly HIV to animals results in ... nothing.

    Stugatz.

    That's right - directly administering the Virus That Causes AIDS™ to animals does not cause AIDS.

    "The only animals susceptible to experimental HIV-1** infection are the chimpanzee, gibbon ape, and rabbit but AIDS-like disease has not yet been reported in these species," lamented the authors of a 1989 FASEB paper.

    Oops.

    I'm guessing those chimps, gibbons and wascawwy wabbits didn't have a history of syphilis, smoking crack or inhaling poppers.

    Experiments in which human volunteers are deliberately 'infected' with the 'HIV isolate' would never get past the ethics committees of most research institutions.

    We do, however, have numerous instances of involuntary infection to give us a guide as to what happens when otherwise low-risk individuals are exposed to 'HIV.'

    In a 1984 NEJM letter, before 'HIV' testing became available, Sloan Kettering researchers reported there had been 27 parenteral exposures by 25 staff to the blood of AIDS patients since August 1982 (24 exposures were via needlestick).

    "All the involved staff are in their usual (generally excellent) state of health," including those who were exposed more than 12 months ago. Blood work was available for 12 staff with exposure more than 6 months prior, and no abnormalities were evident, reported the researchers.

    During 1985–2013, 58 confirmed and 150 possible cases of occupationally acquired HIV infection among healthcare workers were reported to the CDC. Since 1999, only one confirmed case (a laboratory technician sustaining a needle puncture while working with a live HIV culture in 2008) has been reported. There is no mention of subsequent AIDS, something the fear-porn agents at the CDC would surely have mentioned had it occurred.

    Some of you have probably heard of Dr Robert Willner, who twice deliberately pricked himself on TV with blood from 'HIV-positive' men (in Spain 1993, and USA 1994). Willner was an outspoken critic of the HIV hypothesis, having authored a book titled Deadly Deception: The Proof that Sex and HIV Absolutely Do Not Cause AIDS. Depending on who you listen to, Willner died 3 months after his 1994 TV appearance in a car crash, or the following year from a heart attack. Neither outcome is consistent with the oft-cited sequelae of AIDS.

    Jump, Jump, Jump Around

    Despite the fact that it is scientifically untenable, the HIV theory of AIDS still reigns supreme. Which brings us back to the key question: Why did 'HIV' wait until Wham! and Devine hit the charts before it started striking down gay blokes en mass?

    Enter the apes.

    According to Wikipedia, "HIV made the jump from other primates to humans in west-central Africa in the early-to-mid-20th century." (Bold emphasis added)

    Just like Sars-Cov-2 was purported to have kicked off when the allegedly zoonotic virus "jumped" to humans from a bat or pangolin at a Wuhan wet market that did not sell any bats or pangolins.

    Says Wikipedia, "Scientists generally accept that the known strains (or groups) of HIV-1 are most closely related to the simian immunodeficiency viruses (SIVs) endemic in wild ape populations of West Central African forests." (Bold emphasis added).

    "Generally accept" is code for "Scientists have no proof of this, but pretend it's true anyway."

    This brings us to an oft-cited 2011 paper titled "Origins of HIV and the AIDS Pandemic" which repeats the claim that "simian immunodeficiency viruses (SIVs) ... crossed from monkeys to apes and from apes to humans." The paper was authored by Paul Sharp and Beatrice Hahn, the latter a member of Gallo's NCI lab team which she joined in 1982.


    A chimpanzee minding his own business while a Gallo associate who blames apes for spreading HIV to humans (Beatrice Hahn) stares at him from a distance.
    In their paper, the researchers provide a graphic claiming SIV resulting in HIV-1 has been transmitted to humans via chimpanzees and gorillas.

    Hold that thought.

    According to the official narrative, the primary routes of 'HIV' transmission in humans are sexual intercourse with an infected individual, sharing needles with an infected person while taking drugs, transfusions of infected blood, or transmission from an infected pregnant mother to fetus.

    Sharp and Hahn speculate that SIVs first developed in chimpanzees, and were spread among the chimpanzee community primarily through sexual activity, from infected mothers to infants, and "in rare cases, possibly by aggression."

    But how did the disease "jump" from apes to humans? Researchers can't claim humans and apes were shooting up drugs together and sharing needles while doing so, or that apes were administering blood transfusions to humans, because that would be patently absurd.

    Ditto for suggesting apes were passing SIV to humans via birth, because apes don't give birth to humans.

    Claiming that apes transmitted SIV to humans because they were having cross-species sexual encounters would also be a hard sell. Humans are capable of some pretty weird and degenerate behaviour, but good luck pinning down a chimp or gorilla while you attempt to get jiggy with it.


    Meet Bruce. Can bench press you and your extended family with one arm. Incursions into his personal space not advised.
    "How humans acquired the ape precursors of HIV-1 groups M, N, O, and P is not known," write Sharp and Hahn, "however, based on the biology of these viruses, transmission must have occurred through cutaneous or mucous membrane exposure to infected ape blood and/or body fluids. Such exposures occur most commonly in the context of bushmeat hunting." (Bold emphasis added).

    Researchers can't explain exactly how immunodeficiency viruses pole-vaulted from apes to human, so they simply assume it must have happened during hunting expeditions.

    Virologists do a lot of assuming.

    Sharp and Hahn write that the first clue to HIV-1's "sudden emergence, epidemic spread, and unique pathogenicity" came in 1986 when a “morphologically similar but anti-genically distinct” virus was allegedly found to cause AIDS in patients in western Africa.

    Well riddle me this, Batman: Humans have been around for 2.5 million years, and the earliest Homo sapiens were getting around some 300,000 years ago.

    We've been hunting that whole time.

    Furthermore, the advance of agriculture and the steadily declining numbers of hunter-gatherers in modern times would have meant a greatly reduced opportunity for SIV to jump aboard the H-train via scratchy-bitey-fluid-exchangey hunting confrontations.

    Yet immunodeficiency viruses waited until the latter half of the Twentieth Century to successfully make the big cross-species jump?

    What an utter crock.

    Wikipedia admits "How the SIV virus would have transformed into HIV after infection of the hunter or bushmeat handler from the ape/monkey is still a matter of debate."

    Translated: There is no actual scientific evidence to support the claim that, after allegedly entering the human body, ‘SIV’ magically transformed into ‘HIV.’

    The Sodomy Paradox

    There's another problem with the official AIDS narrative which holds that, after catching SIV from apes during hunting mishaps in Africa, it "transformed" into HIV, which hunter-gatherers then spread by doing the backdoor boogie with gay abandon.

    That story further holds that, somewhere along the way, one of these HIV-carrying ape-hunters nailed a gay airline steward from America. Patient Zero then flew back to the US, and began having lots of AIDS-causing unprotected sex in the saunas of San Francisco. Or the gay bars of New York. Or the wet markets of Wisconsin, I'm not sure, all this virus BS gets a bit hard to keep track of after a while.

    It doesn't really matter, because like the rest of the AIDS tale, the gay airline steward story was nonsense. Gaetan Dugas, the French-Canadian flight attendant posthumously labelled 'Patient Zero' and accused of single-handedly igniting the spread of HIV/AIDS across North America, was later exonerated.

    Thanks to the determined sleuthing of Pullitzer Prize-winning reporter John Crewdson, it was known by 1988 that what we now call AIDS was in fact present in America in the 1960s. While the rest of the media was tripping over itself to blame Dugas (“THE MAN WHO GAVE US AIDS” blared the New York Post’s October 6, 1987 headline; “Canadian Said to Have Had Key Role in Spread of AIDS,” wrote the New York Times, while the National Review nicknamed Dugas “the Columbus of AIDS"), Crewdson had discovered a 1973 case report that showed the official Patient Zero story was bollocks.

    That 1973 case report described Robert Rayford, a 15-year-old black lad from St. Louis who had died of AIDS in 1969 - more than a decade before anyone knew what AIDS was. The impoverished teen had presented to hospital in the spring of 1968 with swollen loins covered with open, infected sores. He struggled while breathing, was razor thin and pale as a ghost. Doctors initially suspected cancer, but subsequent tests revealed herpes, genital warts, and a severe case of chlamydia. The infection spread, in the form of purple colored lesions, to his legs, causing a misdiagnosis of lymphedema. He eventually succumbed to his condition in May 1969, leaving doctors baffled.

    The teen, who doctors described as mildly intellectually impaired, said he'd suffered the symptoms for around two years prior to seeking medical help. He denied injury or animal bites, had not travelled outside the midwestern United States, but admitted to "frequent" heterosexual intercourse. His family consented to an autopsy, which revealed "widespread Kaposi's sarcoma of the aggressive, disseminated type." The autopsy also found evidence of anal scarring and a particular kind of lesion no one had identified when Rayford was alive. Some doctors thought the scarring indicated Rayford was gay; others pointed out he may have been sexually abused.

    Struck by how closely Rayford's symptoms resembled those of AIDS, Crewdson flew to St. Louis and found a pathologist willing to dig through laboratory freezers in search of the youth's tissue samples. By using the test 'co-developed' by Gallo and the French, researchers were able to determine that the boy, incredibly, had been infected with 'HIV.'

    The finding was published in JAMA in 1988. However, it was not until 2016 that the fake Dugas tale was officially revoked.

    Had the Rayford story been more widely known, it wouldn’t have been good for HIV business.

    Not to worry, the out-of-Africa hypothesis was salvaged in 1998 when researchers claimed they had detected HIV - by a PCR process involving two rounds of amplification for a combined total of 69 cycles - in a plasma sample obtained in early 1959 from an adult Bantu male, with a sickle-cell trait and a glucose-6-phosphate-dehydrogenase deficiency, living in the Belgian Congo. Two of the researchers announcing this narrative-saving discovery hailed from the Aaron Diamond AIDS Research Center, at Rockefeller University in New York.

    So just like the COVID charade, we have a shamdemic for which the original Patient Zero story was shown to be a bunch of cobblers. Just like the COVID sham, few people noticed or cared and the rest of the AIDS tale continued its relentless march and took on a life of its own.

    Despite more holes than a ... wait, that's dangerous pun territory ... I mean, despite a plethora of discrepancies, the official Fauci-endorsed tale still has HIV migrating from Africa to the US and spread in the early 1980s by blokes bumping uglies in big city gay bars and saunas.

    And Fauci should know, because he went to gay saunas and gay bars himself in the “early stages” of the AIDS “explosion” to get a “feel” for the situation.

    Purely for ‘research’ purposes, of course (wink, wink).

    It's okay Tony, it's 2024, you don't have to cover for your sexuality anymore.


    A young Anthony Fauci displaying his "I've just been to the saunas!" smile. Your tax money at work.
    You could literally fill a book with all the discrepancies contained within the official AIDS story; several authors have already done just that. What I wanted to highlight here are the commonalities between the AIDS and COVID sagas.

    Both featured never-isolated 'viruses' with nonsensical 'Patient Zero' stories.

    ‘Isolates’ of both these ‘deadly’ and ‘novel’ viruses do a whole lot of nothing when administered to our primate cousins.

    Both sagas featured Anthony Fauci, showing up on cue touting the most toxic drug he could get away with recommending.

    Both featured doomsday, end-of-times hyperbole in which testing 'positive' was initially considered a death sentence.

    Both were remarkable demonstrations of how the media and masses could be easily manipulated into accepting a pandemic scare that, upon the most cursory examination, simply didn't add up.


    *During the presidency of former actor Ronald Reagan, senior administration officials secretly — and illegally — arranged for the sale of arms to Iran in return for Iran’s promise to help secure the release of a group of Americans being held hostage in Lebanon.

    Suspiciously, the hostages were formally released into US custody just minutes after Reagan was sworn into office.

    Proceeds from the arms sales were then secretly, and again illegally, funneled to the Contras, a group of rebels fighting the Marxist Sandinista government of Nicaragua.

    Is if that wasn't bad enough, the CIA looked the other way while the Contras trafficked cocaine into the US to help finance their fight to oust the communist Sandinistas. The scandal was exposed in 1996 by the brilliant, Pullitzer Prize-winning journalist Gary Webb while writing for the San Jose Mercury News. His series described a San Francisco Bay Area drug ring that sold tons of cocaine to the Crips and Bloods street gangs of Los Angeles, funelling millions in drug profits to the CIA-assisted Contras. This drug ring "opened the first pipeline between Colombia's cocaine cartels and the black neighborhoods of Los Angeles" and, as a result, "helped spark a crack explosion in urban America."

    His articles caused a proverbial shit-storm, prompting the government to conduct several investigations into itself and declaring itself innocent of all charges. We were supposed to believe it was all just an accidental oversight when even the Kerry report acknowledged "the Contra drug links included", among other connections, "... payments to drug traffickers by the U.S. State Department of funds authorized by the Congress for humanitarian assistance to the Contras, in some cases after the traffickers had been indicted by federal law enforcement agencies on drug charges, in others while traffickers were under active investigation by these same agencies." (Bold emphasis added).

    The Los Angeles Times, New York Times, and Washington Post launched their own 'investigations' (read: hatchet jobs) and rejected Webb's allegations, instead siding with the government - a practice they uphold to this day.

    However, an internal CIA report released in 1998 admitted the CIA ‘overlooked’ or ‘ignored’ reports that the Nicaragua Contra rebels financed their fight to oust the communist Sandinistas through the sale of drugs in the United States.

    **‘HIV-1’ is the form of ‘HIV’ allegedly most common and threatening to humans. According to the official tale, ‘HIV-2’ is rare and of little threat.

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    Why the Official AIDS Story is a Complete Crock The Great Rebranding, 1980s-Style: HIV Was a Sham, Just Like Sars-Cov-2 Anthony Colpo All you youngsters born after the Glomesh era have surely heard of AIDS, but probably have no idea of just how big a deal it was when it burst onto the scene in the early 1980s. It was the biggest show in town. Sure, it wasn't as big a deal as what COVID would later be. It wasn't accompanied by 'vaccine' mandates, lockdowns or heavily-armed goons bashing people for sitting peacefully in the park. Instead of masks, there were condoms and paper toilet seat covers. There was no social distancing, only admonitions to avoid unprotected sex and not share needles when shooting up. Fauci was there, front and center, but he wasn't telling us to wear two condoms at once. Instead, he was pimping a toxic concoction known as AZT. Right off the bat, nothing made sense about the AIDs charade. It does make sense in hindsight if you view it as a giant test run, an exercise in spreading 'virus' hysteria. The HIV/AIDS charade confirmed most people don't ask questions, and those who do can be quickly shouted over and marginalized as "deniers," "conspiracists" and menaces to society. It also confirmed that not only could people be convinced to take toxic drugs in response to an overblown 'pandemic' scare, but they could be manipulated into rabidly demanding their expedited release. It was an exercise whose lessons would prove valuable come December 2019. AIDS stands for "acquired immunodeficiency syndrome." In other words, you somehow "acquired" an immune system that, like a tired car engine with 300,000 km on the clock, was about to blow its last gasket. It was first identified in 1981 in Los Angeles when the CDC reported on five young homosexual men suffering pneumonia caused by a protozoon known as Pneumocystis carinii. This microbe is ordinarily innocuous and, in fact, found in nearly all healthy persons. For reasons unknown it had suddenly become lethal - an outcome previously seen only in persons whose immune systems were being undermined by immunosuppressant therapy, cancer, or severe malnourishment. This same pneumonia promptly appeared in New York, together with several dozen cases of an unusual skin cancer called Kaposi's Sarcoma which had previously been almost unknown in the US. Eventually Pneumocystis carinii pneumonia and Kaposi's Sarcoma were interpreted as secondary manifestations of an underlying immune-system deficiency of unknown origin which was eventually dubbed "acquired immunodeficiency disease syndrome" or AIDS. The bodies of AIDS patients seemed to have just given up. Patients suffered severe weight loss and lethargy and were so immune deficient that even a minor infection threatened to kill them. The first few thousand cases were found mostly in homosexual males, and the media bombarded us with images of emaciated gay blokes on the verge of death and barely able to sit upright. Initially, the condition was referred to as GRID (gay-related immune deficiency). Outside of scientific circles, it came to be known as the "gay plague" and religious fundamentalists trumpeted the phenomenon as God's revenge on evil sodomites. That began to change in 1983, when AIDS was found to affect heterosexual women, which caused the fear porn to increase by an order of magnitude. As with COVID, health authorities treated us to an orgy of fearmongering and doomsday predictions - and the sheeple lapped it up. In 1986, Dr. Donald Ian Macdonald, then Acting Assistant Secretary of Health and Human Services, described "the escalating AIDS epidemic" as "staggering," "devastating" and a "huge problem." Dr. Halfdan Mahler, Danish physician and head of the World Health Organization, called AIDS "a health disaster of pandemic proportions" and said he could "not imagine a worse health problem in this century." "We stand nakedly in front of a very serious pandemic as mortal as any pandemic there ever has been," Mahler bizarrely quipped. Why he would don his birthday suit instead of a Hazmat one in the face of such a mortal pandemic was never explained, but that's globalist bureaucrats for you. "I don't know of any greater killer than AIDS, not to speak of its psychological, social and economic maiming," continued Mahler, who after leaving WHO became director of the International Planned Parenthood Federation. Not to be outdone, in 1987 Harvard biology professor Stephen Jay Gould, said AIDS was "potentially, the greatest natural tragedy in human history." He warned "AIDS may run through the entire population, and may carry off a quarter or more of us" (in 1987, the world population was just over 5 billion; it now stands at over 8 billion). That same year, Gallup asked an open-ended question about what Americans saw as the most urgent health problem facing the US. Despite the fact AIDS has never even come close to being the leading cause of death in the US, more than two-thirds of Americans said AIDS. The disease continued as the top pick until 2000. According to Gallop polls conducted in 1987, most Americans (60%) agreed people with AIDS should be made to carry a card noting they had the disease, and one in three (33%) agreed employers should be allowed to fire employees who had AIDS. Twenty-one percent of Americans said people with AIDS should be isolated from the rest of society. An earlier LA Times poll from 1985 found more than half of US adults supported quarantining AIDS patients, nearly half would approve of ID cards for those testing positive for "AIDS antibodies," and one in seven favored tattooing those with the disease. People never learn. A Disease Looking For a Cause Authorities had presented us with a new public health scare, but no causal agent. No-one knew what caused the immune systems of AIDS patients to become so deficient. Was it a new microbe? A new drug scourge? God's revenge for Abba and Disco Duck? No-one knew. At least officially. In reality, authorities knew damn well what was going on. But they didn’t tell us. Instead, they eventually claimed AIDS was the result of a 'novel virus' that, in 1986, was named "human immunodeficiency virus,” or HIV. The 'novel virus' paradigm holds that a 'zoonotic' virus wakes up one day, and decides to "jump" from apes/bats/pangolins/garden gnomes to humans. This novel virus then acts like a seventeen year old that has been given the keys to an alcohol-filled mansion while mom and dad head off for a weekend vacation. However, the virus has no friends to party with. So he first has to convert to a 'human' form of the virus, then he has to begin self-replicating in order to build a social circle. Once this is done, the virions party so hard that the host becomes sick. The virions conclude their current host is no fun, so they go looking for a new host to party inside. The process repeats itself, and before you know it, there's a 'pandemic' going on with squillions of little virions pogo-dancing in global synchrony and chanting "the roof, the roof, the roof is on fire!!" while trashing everything in sight. Viruses these days, sheesh. Setting aside the glaring fallacies of the virus 'isolation' charade, the 'novel virus = pandemic’ theory is an inherent load of cobblers. Outbreaks of what look to be infectious illnesses don't just happen for no reason. There has to be some facilitating factor. AIDS became a big thing in the early 1980s, and we know that initially, the majority of patients were gay males. African-Americans were also known to be at increased risk. Even if butt sex is an especially efficient method of transmitting STDs, it doesn't explain why AIDS became a phenomenon in the 1980s. After all, both sodomy and homosexuality have been around as long as humans have. Heck, even apes have been observed taking rides on the Hershey Highway. Which begs the question: What other events with the potential for dire impact on health occurred around the same time as the AIDS outbreak? The Other Crack Rears Its Ugly Head Thanks in no small part to Uncle Sam and his ability to conveniently look the other way when it suits his financial and geopolitical interests*, the early 1980s saw a massive flood of cocaine into the US, with urban black neighborhoods the worst afflicted. So plentiful was the supply of cocaine, drug dealers came up with a way to make it even cheaper and more addictive in order to expand their customer base. Freebase is the name given to the original form of smokable coke, which resulted in a more intense high than snorting. While this constituted an obvious selling point, the process for making freebase required ether, making it notoriously volatile and dangerous to produce. In a famed 1980 incident, comedian Richard Pryor suffered severe and life-threatening burns after mixing cocaine with ether at his home; the mixture promptly exploded in his face. Freebase cocaine seems to have first surfaced in the US in the mid-1970s. Around 1980, a less volatile but similar process was developed by dealers in which cocaine was dissolved in a solution of water and baking soda and then dried out into "crack rocks." As the rocks are heated, it makes a crackling sound, hence the name. As early as 1981, reports of crack appeared in Los Angeles, San Diego, Houston, and in the Caribbean. Its use quickly spread to other major US cities, and by 1987, crack was reportedly available in DC and all but four states in the Union. "In some major cities, such as New York, Detroit, and Philadelphia, one dosage unit of crack could be obtained for as little as $2.50," writes the US DEA. "Never before had any form of cocaine been available at such low prices and at such high purity." The crack epidemic dramatically increased the number of Americans addicted to cocaine, as well as the number of cocaine-related hospital emergencies. In 1985, cocaine-related hospital emergencies rose by 12 percent, from 23,500 to 26,300. In 1986, these incidents increased 110 percent, from 26,300 to 55,200. The crack cocaine explosion, you'll notice, overlaps neatly with the AIDS "explosion." The House of Representatives Select Committee on Narcotics Abuse and Control held cocaine hearings in July, October, and November 1980. Dr. Robert Byck, who along with his colleagues conducted the first scientific studies of cocaine plasma levels after coca paste smoking, testified at the hearings. He warned that the heavy use of smokable freebase cocaine, employed by an estimated 10 percent of cocaine users, was about to change. He warned Congress that the US was about to experience the worst epidemic of drug abuse the country had ever seen. Byck predicted the use of smoked cocaine in the 1980s would match the widespread use of "speed" (methamphetamine) in the 1960s. He urged Congress and the National Institute on Drug Abuse to mount an education and prevention campaign to avert this impending epidemic. No such campaign was undertaken. "The emergence of crack cocaine use in the United States during the mid-1980s was one of the most significant public health problems of that era," note Watkins et al in a 1998 paper. "Crack use contributed to a series of sexually transmitted disease epidemics, to epidemic increases in violent injuries and homicides, and to significant increases in the incidence and prevalence of cocaine addiction. Despite these threats to health and safety, a national public health campaign to counter crack-related morbidity and mortality was never mounted." Is that because authorities were already committed to carrying out a manufactured 'HIV' crisis? Crack, Risky Sex, and 'HIV' A 1994 NEJM article reported an analysis of 1,967 people recruited from inner-city neighborhoods in New York, Miami, and San Francisco. All respondents reported never having injected drugs, however 1,137 were regular smokers of crack. The remaining 830 people reported never having smoked crack. The results for crack users weren't pretty. Female crack users were 4.1 times more likely to have been raped, and 1.6 times more likely to have had their first vaginal or anal sex encounter before 13 years of age. Both male and female crack users reported a higher number of sexual partners than non-users; in the case of women, crack users were 11 times more likely to have had 50 or more sexual partners. Crack-smoking women were 13.5 times more likely than nonsmoking women to have engaged in sexual work at any time, and 28.8 times more likely to have engaged in recent, unprotected sex work. Male crack smokers, meanwhile, were 3.4 times more likely to report ever having homosexual anal sex, and 23 times more likely to have had 50 or more male anal sex partners. Clearly, crack users were significantly more likely to engage in prostitution and risky sexual practices. Not surprising then, that female and male crack users had higher historical rates of syphilis (3.5 and 2.2, respectively) and gonorrhea (1.8 and 1.6, respectively). When the researchers ran blood tests for current infection, female and male crack users were significantly more likely to test positive for syphilis (2.8 and 1.6, respectively). Among the participants in New York and Miami, HIV 'infection' was 2.3 times more prevalent among crack smokers than among nonsmokers (prevalence of HIV antibodies among participants recruited in San Francisco was low). Testing positive for ‘HIV antibodies’ was strongly associated with previous or current infection with other STDs. A positive reactive syphilis test (adjusted odds ratio, 2.3) and a history of herpes (adjusted odds ratio, 3.6) remained significantly associated with HIV infection after adjustment for high-risk sexual practices and African-American race. Other studies found similar results. Chiasson and colleagues at the New York City Department of Health examined the link between HIV infection and crack use. Examining patients at an STD clinic in the South Bronx, they found that, among women with no other identified risk (i.e., no injectible drug use), crack use, prostitution, crack-using prostitution and history of syphilis were all found to be risk factors for HIV infection. Among men with no other risk behavior, a history of syphilis was in fact the strongest predictor of HIV infection - greater than crack use and contact with prostitutes. In a 1990 paper, Greenspan and Castro note "between 1981 and 1983, the incidence of primary and secondary syphilis in the United States increased 34%, reaching a rate in 1989 (18.4 cases per 100,000 persons) that was higher than at any time since 1949. Between 1985 and 1989, incidence among blacks more than doubled, from 52.5 to 121.8 cases per 100,000; the increase was greater for black women than for black men (176% versus 106%). These trends are markers for the same high-risk sexual practices that promote transmission of HIV." So crack, syphilis and ‘HIV’ are closely related. Now let's look at another class of drugs showing a close correlation with pre-existing STDs and ‘HIV.’ The Popper Phenomenon “Poppers” is a slang term for nitrite inhalant drugs (when they were first manufactured, they came in small ampoules that were 'popped' to release fumes). Amyl nitrite was originally developed to treat angina pectoris by dilating blood vessels, allowing the heart to get more oxygen and thereby relieving the pain. Arteries are not the only thing poppers help to dilate. Inhaling nitrites relaxes smooth muscles throughout the body - including the sphincter muscles, making it particularly helpful to gay posteriors. Along with facilitating anal sex, the blood vessel-dilating effects of poppers can produce a brief but intense sensation of heat and euphoria lasting 1 or 2 minutes. The story of poppers is an interesting one, involving US Vietnam vets, a profiteering Big Pharma and an enabling FDA, a gay medical student and organized criminals. The latter two entities sidestepped an eventual prescription requirement for amyl nitrite by creating butyl and isobutyl nitrite - less pure, more toxic, and even faster-acting versions than the original. Further restrictions were averted thanks to an unwritten agreement between producers and the FDA that poppers were only to be advertised in gay-oriented publications, as 'room deodorizers.' During the 1970s and early 80s, poppers were advertised heavily in the gay press, and the drugs became an integral part of gay culture. Not only was it routine for patrons at gay nightclubs to freely pass the vials around, some "disco clubs would even add to the general euphoria by occasionally spraying the dance floor with poppers fumes." "The miasma of nitrite fumes was taken for granted at gay gathering places: bars, baths, leather clubs," writes John Lauritsen in a 1994 New York Native article. "Some gay men were never without their little bottle, from which they snorted fumes around the clock." Throwing caution to the wind when it comes to drugs never ends well. Amyl nitrite was developed for occasional use by angina patients, not as a party drug to be snorted every time one hit the dance floor or engaged in a bout of Jolly Rogering. Apart from causing localized damage to nasal membranes, poppers have been linked to anemia, strokes, heart, lung, and brain damage, cardiovascular collapse, and, tellingly, the blood de-oxygenation, thymus atrophy, chronic depletion of T-cell ratio's associated with severe immune dysfunction. The drugs have also been linked to the development of Kaposi's Sarcoma. Sounds a lot like AIDS, doesn't it? While researchers and the more level-headed of gay advocates warned of the dangers, the FDA continued to look the other way. The gay press, whose advertising revenue relied heavily on popper ads, also willfully turned a blind eye to the dangers. In the 1980s, in a lukewarm attempt to be seen to be doing something about the problem, US health officials banned the use of poppers in public places and required merchants to post warnings about their dangers. "The warnings about their use disappeared sometime in the late '80s to early '90s," reports SFGATE, "and no one seems to know why." "During the first few years of the AIDS epidemic," writes Ian Young at VirusMyth.org, "poppers came under suspicion as a possible contributing factor. But after 1984, when the Reagan administration pronounced a single retrovirus to be the only cause of the growing list of AIDS illnesses, the health hazards of poppers were dismissed. All attention and funding was directed to HIV." Fun fact: Burroughs Wellcome, the original manufacturers of poppers, went on to profit handsomely from the subsequent AIDS hysteria with its highly-toxic 'anti-AIDS' drug AZT. History is Made (Up) There were major drug scourges afflicting the high-risk gay and African-American communities, drugs whose chronologies overlapped neatly with the AIDS outbreak. Use and abuse of these drugs was well established to cause severe illness, immune dysfunction and was also strongly correlated with pre-existing STDs like syphilis. The powers-that-be, however, had already decided the sole cause of AIDs was a 'novel virus.' They just needed to come up with one. And so along came the virologists to save the day. Not just any old bunch of virologists, but virologists with friends in high places. In France, this meant Luc Montagnier and his team at the Pasteur Institute, which advises the French government and the World Health Organization (WHO), and maintains a close collaboration with the US Centers for Disease Control and Prevention (CDC). In the US, it meant sci-bureaucrats from the government's behemoth National Institutes of Health (NIH). One of the key figures was the caustic Robert S Gallo, a researcher at the NIH's National Cancer Institute, where he worked for 30 years mainly as head of the Laboratory of Tumor Cell Biology. Gallo’s career would be dogged by controversy and misconduct allegations, but that’s a whole other article (stay tuned). The other career bureaucrat that would play a key role on the US side was none other than Anthony S Fauci, who recently completed a ridiculous 38-year reign as unelected head of the NIH's National Institute of Allergy and Infectious Diseases (NIAID). If you've surmised that, with names like the above, the HIV story must be a real shite show, you are absolutely correct. HIV is Invented 'Discovered' In 1983, the Pasteur Institute researchers declared they had 'isolated' a 'retrovirus' belonging to the family of T-cell leukemia viruses (HTLV), and concluded it "may be involved in several pathological syndromes, including AIDS." (Bold emphasis added) Their isolate came from a promiscuous 33-year-old Caucasian homosexual male referred to as "BRU", who indicated he'd had more than 50 sexual partners per year. Nasty. According to the authors, he displayed "signs and symptoms that often precede the acquired immune deficiency syndrome (AIDS)." However, the only symptoms reported for the patient were multiple lymphadenopathies (swollen lymph glands) and asthenia (weakness), which are evident in many conditions aside from AIDS. Neither fever nor recent loss of weight were noted. In other words, the patient from whom the alleged AIDS-causing virus was first 'isolated' from did not have an AIDS diagnosis. Tellingly, the patient did have a history of several episodes of gonorrhea and had been treated for syphilis in September 1982. Lymphadenopathy is one of the symptoms of both the aforementioned infections. The study's lead author was Francoise Barre-Sinoussi, although the finding is routinely credited to the paper's last listed author, the late Montagnier. The French study was marred by two key problems. It did not isolate any virus, and it did not show AIDS was caused by any HTLV offshoot. Forty years later, little has changed. The terminology and rationalizations have indeed become increasingly complex (as is the case with most elaborate lies), but there is no physical isolate of 'HIV.' Virologists and their sycophants, of course, insist this doesn't matter and that their non-purified mixtures are indeed isolates. While they condescendingly sneer and dismiss anyone who disputes this as a silly little dumb-dumb that doesn't 'understand' virology, they tend to remain rather quiet on another highly inconvenient observation. Namely, there is no proof that whatever is in their ‘isolates’ actually causes AIDS. HIV and Sars-Cov-2: The 'Deadly' Viruses That Aren't Deadly In the early days of 'COVID', testing positive for the mythical Sars-Cov-2 was considered a death sentence. So much so, that some folks didn't even bother getting their affairs in order; they instead killed themselves. Such is the power of all this heinous "deadly virus" bullshit. It was the same in the 'HIV' Dark Ages - testing positive was considered a death sentence. When a famous basketballer by the name of Erving “Magic” Johnson announced he was HIV positive in 1991, everyone was shocked. "Now we all know someone with HIV," said someone I can't recall in what was supposed to be a profound, insight-triggering moment. Johnson, everyone assumed, was now living on borrowed time. Thirty-three years later, Johnson is still alive and wealthy. He attributes his survival to antiretroviral cocktails that have never been shown in clinical studies to benefit survival: GlaxoSmithKline's Trizivir and Abbott's Kaletra. These cocktails are comprised of drugs like AZT which increase the risk of side effects but have never been shown to exert a mortality benefit. Johnson, it should be noted, has featured in ads for both products. In 2009, the FDA issued a warning letter to Abbott Laboratories regarding a promotional DVD in which Johnson discussed his experiences with Kaletra. The letter stated the violations were of public health concern "because they suggest that Kaletra is safer and more effective than has been demonstrated by substantial evidence or substantial clinical experience, and encourage use in circumstances other than those for which the drug has been shown to be safe and effective." "FDA is not aware of substantial evidence or substantial clinical experience to support effectiveness for five or more years of treatment with Kaletra in treatment-experienced adults. The personal experience of Kaletra patients, such as Magic Johnson, does not constitute such evidence." So if overpriced drug cocktails aren't keeping Johnson alive, what explains his survival? It's explained by the fact that HIV is a load of bollocks. A shady test that claims you are ‘HIV positive’ does not mean you are in fact harboring a deadly 'virus.' If ‘HIV’ was so deadly, then lab animals infected with it would get sick and die. But guess what? Administering a so-called isolate of uber-deadly HIV to animals results in ... nothing. Stugatz. That's right - directly administering the Virus That Causes AIDS™ to animals does not cause AIDS. "The only animals susceptible to experimental HIV-1** infection are the chimpanzee, gibbon ape, and rabbit but AIDS-like disease has not yet been reported in these species," lamented the authors of a 1989 FASEB paper. Oops. I'm guessing those chimps, gibbons and wascawwy wabbits didn't have a history of syphilis, smoking crack or inhaling poppers. Experiments in which human volunteers are deliberately 'infected' with the 'HIV isolate' would never get past the ethics committees of most research institutions. We do, however, have numerous instances of involuntary infection to give us a guide as to what happens when otherwise low-risk individuals are exposed to 'HIV.' In a 1984 NEJM letter, before 'HIV' testing became available, Sloan Kettering researchers reported there had been 27 parenteral exposures by 25 staff to the blood of AIDS patients since August 1982 (24 exposures were via needlestick). "All the involved staff are in their usual (generally excellent) state of health," including those who were exposed more than 12 months ago. Blood work was available for 12 staff with exposure more than 6 months prior, and no abnormalities were evident, reported the researchers. During 1985–2013, 58 confirmed and 150 possible cases of occupationally acquired HIV infection among healthcare workers were reported to the CDC. Since 1999, only one confirmed case (a laboratory technician sustaining a needle puncture while working with a live HIV culture in 2008) has been reported. There is no mention of subsequent AIDS, something the fear-porn agents at the CDC would surely have mentioned had it occurred. Some of you have probably heard of Dr Robert Willner, who twice deliberately pricked himself on TV with blood from 'HIV-positive' men (in Spain 1993, and USA 1994). Willner was an outspoken critic of the HIV hypothesis, having authored a book titled Deadly Deception: The Proof that Sex and HIV Absolutely Do Not Cause AIDS. Depending on who you listen to, Willner died 3 months after his 1994 TV appearance in a car crash, or the following year from a heart attack. Neither outcome is consistent with the oft-cited sequelae of AIDS. Jump, Jump, Jump Around Despite the fact that it is scientifically untenable, the HIV theory of AIDS still reigns supreme. Which brings us back to the key question: Why did 'HIV' wait until Wham! and Devine hit the charts before it started striking down gay blokes en mass? Enter the apes. According to Wikipedia, "HIV made the jump from other primates to humans in west-central Africa in the early-to-mid-20th century." (Bold emphasis added) Just like Sars-Cov-2 was purported to have kicked off when the allegedly zoonotic virus "jumped" to humans from a bat or pangolin at a Wuhan wet market that did not sell any bats or pangolins. Says Wikipedia, "Scientists generally accept that the known strains (or groups) of HIV-1 are most closely related to the simian immunodeficiency viruses (SIVs) endemic in wild ape populations of West Central African forests." (Bold emphasis added). "Generally accept" is code for "Scientists have no proof of this, but pretend it's true anyway." This brings us to an oft-cited 2011 paper titled "Origins of HIV and the AIDS Pandemic" which repeats the claim that "simian immunodeficiency viruses (SIVs) ... crossed from monkeys to apes and from apes to humans." The paper was authored by Paul Sharp and Beatrice Hahn, the latter a member of Gallo's NCI lab team which she joined in 1982. A chimpanzee minding his own business while a Gallo associate who blames apes for spreading HIV to humans (Beatrice Hahn) stares at him from a distance. In their paper, the researchers provide a graphic claiming SIV resulting in HIV-1 has been transmitted to humans via chimpanzees and gorillas. Hold that thought. According to the official narrative, the primary routes of 'HIV' transmission in humans are sexual intercourse with an infected individual, sharing needles with an infected person while taking drugs, transfusions of infected blood, or transmission from an infected pregnant mother to fetus. Sharp and Hahn speculate that SIVs first developed in chimpanzees, and were spread among the chimpanzee community primarily through sexual activity, from infected mothers to infants, and "in rare cases, possibly by aggression." But how did the disease "jump" from apes to humans? Researchers can't claim humans and apes were shooting up drugs together and sharing needles while doing so, or that apes were administering blood transfusions to humans, because that would be patently absurd. Ditto for suggesting apes were passing SIV to humans via birth, because apes don't give birth to humans. Claiming that apes transmitted SIV to humans because they were having cross-species sexual encounters would also be a hard sell. Humans are capable of some pretty weird and degenerate behaviour, but good luck pinning down a chimp or gorilla while you attempt to get jiggy with it. Meet Bruce. Can bench press you and your extended family with one arm. Incursions into his personal space not advised. "How humans acquired the ape precursors of HIV-1 groups M, N, O, and P is not known," write Sharp and Hahn, "however, based on the biology of these viruses, transmission must have occurred through cutaneous or mucous membrane exposure to infected ape blood and/or body fluids. Such exposures occur most commonly in the context of bushmeat hunting." (Bold emphasis added). Researchers can't explain exactly how immunodeficiency viruses pole-vaulted from apes to human, so they simply assume it must have happened during hunting expeditions. Virologists do a lot of assuming. Sharp and Hahn write that the first clue to HIV-1's "sudden emergence, epidemic spread, and unique pathogenicity" came in 1986 when a “morphologically similar but anti-genically distinct” virus was allegedly found to cause AIDS in patients in western Africa. Well riddle me this, Batman: Humans have been around for 2.5 million years, and the earliest Homo sapiens were getting around some 300,000 years ago. We've been hunting that whole time. Furthermore, the advance of agriculture and the steadily declining numbers of hunter-gatherers in modern times would have meant a greatly reduced opportunity for SIV to jump aboard the H-train via scratchy-bitey-fluid-exchangey hunting confrontations. Yet immunodeficiency viruses waited until the latter half of the Twentieth Century to successfully make the big cross-species jump? What an utter crock. Wikipedia admits "How the SIV virus would have transformed into HIV after infection of the hunter or bushmeat handler from the ape/monkey is still a matter of debate." Translated: There is no actual scientific evidence to support the claim that, after allegedly entering the human body, ‘SIV’ magically transformed into ‘HIV.’ The Sodomy Paradox There's another problem with the official AIDS narrative which holds that, after catching SIV from apes during hunting mishaps in Africa, it "transformed" into HIV, which hunter-gatherers then spread by doing the backdoor boogie with gay abandon. That story further holds that, somewhere along the way, one of these HIV-carrying ape-hunters nailed a gay airline steward from America. Patient Zero then flew back to the US, and began having lots of AIDS-causing unprotected sex in the saunas of San Francisco. Or the gay bars of New York. Or the wet markets of Wisconsin, I'm not sure, all this virus BS gets a bit hard to keep track of after a while. It doesn't really matter, because like the rest of the AIDS tale, the gay airline steward story was nonsense. Gaetan Dugas, the French-Canadian flight attendant posthumously labelled 'Patient Zero' and accused of single-handedly igniting the spread of HIV/AIDS across North America, was later exonerated. Thanks to the determined sleuthing of Pullitzer Prize-winning reporter John Crewdson, it was known by 1988 that what we now call AIDS was in fact present in America in the 1960s. While the rest of the media was tripping over itself to blame Dugas (“THE MAN WHO GAVE US AIDS” blared the New York Post’s October 6, 1987 headline; “Canadian Said to Have Had Key Role in Spread of AIDS,” wrote the New York Times, while the National Review nicknamed Dugas “the Columbus of AIDS"), Crewdson had discovered a 1973 case report that showed the official Patient Zero story was bollocks. That 1973 case report described Robert Rayford, a 15-year-old black lad from St. Louis who had died of AIDS in 1969 - more than a decade before anyone knew what AIDS was. The impoverished teen had presented to hospital in the spring of 1968 with swollen loins covered with open, infected sores. He struggled while breathing, was razor thin and pale as a ghost. Doctors initially suspected cancer, but subsequent tests revealed herpes, genital warts, and a severe case of chlamydia. The infection spread, in the form of purple colored lesions, to his legs, causing a misdiagnosis of lymphedema. He eventually succumbed to his condition in May 1969, leaving doctors baffled. The teen, who doctors described as mildly intellectually impaired, said he'd suffered the symptoms for around two years prior to seeking medical help. He denied injury or animal bites, had not travelled outside the midwestern United States, but admitted to "frequent" heterosexual intercourse. His family consented to an autopsy, which revealed "widespread Kaposi's sarcoma of the aggressive, disseminated type." The autopsy also found evidence of anal scarring and a particular kind of lesion no one had identified when Rayford was alive. Some doctors thought the scarring indicated Rayford was gay; others pointed out he may have been sexually abused. Struck by how closely Rayford's symptoms resembled those of AIDS, Crewdson flew to St. Louis and found a pathologist willing to dig through laboratory freezers in search of the youth's tissue samples. By using the test 'co-developed' by Gallo and the French, researchers were able to determine that the boy, incredibly, had been infected with 'HIV.' The finding was published in JAMA in 1988. However, it was not until 2016 that the fake Dugas tale was officially revoked. Had the Rayford story been more widely known, it wouldn’t have been good for HIV business. Not to worry, the out-of-Africa hypothesis was salvaged in 1998 when researchers claimed they had detected HIV - by a PCR process involving two rounds of amplification for a combined total of 69 cycles - in a plasma sample obtained in early 1959 from an adult Bantu male, with a sickle-cell trait and a glucose-6-phosphate-dehydrogenase deficiency, living in the Belgian Congo. Two of the researchers announcing this narrative-saving discovery hailed from the Aaron Diamond AIDS Research Center, at Rockefeller University in New York. So just like the COVID charade, we have a shamdemic for which the original Patient Zero story was shown to be a bunch of cobblers. Just like the COVID sham, few people noticed or cared and the rest of the AIDS tale continued its relentless march and took on a life of its own. Despite more holes than a ... wait, that's dangerous pun territory ... I mean, despite a plethora of discrepancies, the official Fauci-endorsed tale still has HIV migrating from Africa to the US and spread in the early 1980s by blokes bumping uglies in big city gay bars and saunas. And Fauci should know, because he went to gay saunas and gay bars himself in the “early stages” of the AIDS “explosion” to get a “feel” for the situation. Purely for ‘research’ purposes, of course (wink, wink). It's okay Tony, it's 2024, you don't have to cover for your sexuality anymore. A young Anthony Fauci displaying his "I've just been to the saunas!" smile. Your tax money at work. You could literally fill a book with all the discrepancies contained within the official AIDS story; several authors have already done just that. What I wanted to highlight here are the commonalities between the AIDS and COVID sagas. Both featured never-isolated 'viruses' with nonsensical 'Patient Zero' stories. ‘Isolates’ of both these ‘deadly’ and ‘novel’ viruses do a whole lot of nothing when administered to our primate cousins. Both sagas featured Anthony Fauci, showing up on cue touting the most toxic drug he could get away with recommending. Both featured doomsday, end-of-times hyperbole in which testing 'positive' was initially considered a death sentence. Both were remarkable demonstrations of how the media and masses could be easily manipulated into accepting a pandemic scare that, upon the most cursory examination, simply didn't add up. *During the presidency of former actor Ronald Reagan, senior administration officials secretly — and illegally — arranged for the sale of arms to Iran in return for Iran’s promise to help secure the release of a group of Americans being held hostage in Lebanon. Suspiciously, the hostages were formally released into US custody just minutes after Reagan was sworn into office. Proceeds from the arms sales were then secretly, and again illegally, funneled to the Contras, a group of rebels fighting the Marxist Sandinista government of Nicaragua. Is if that wasn't bad enough, the CIA looked the other way while the Contras trafficked cocaine into the US to help finance their fight to oust the communist Sandinistas. The scandal was exposed in 1996 by the brilliant, Pullitzer Prize-winning journalist Gary Webb while writing for the San Jose Mercury News. His series described a San Francisco Bay Area drug ring that sold tons of cocaine to the Crips and Bloods street gangs of Los Angeles, funelling millions in drug profits to the CIA-assisted Contras. This drug ring "opened the first pipeline between Colombia's cocaine cartels and the black neighborhoods of Los Angeles" and, as a result, "helped spark a crack explosion in urban America." His articles caused a proverbial shit-storm, prompting the government to conduct several investigations into itself and declaring itself innocent of all charges. We were supposed to believe it was all just an accidental oversight when even the Kerry report acknowledged "the Contra drug links included", among other connections, "... payments to drug traffickers by the U.S. State Department of funds authorized by the Congress for humanitarian assistance to the Contras, in some cases after the traffickers had been indicted by federal law enforcement agencies on drug charges, in others while traffickers were under active investigation by these same agencies." (Bold emphasis added). The Los Angeles Times, New York Times, and Washington Post launched their own 'investigations' (read: hatchet jobs) and rejected Webb's allegations, instead siding with the government - a practice they uphold to this day. However, an internal CIA report released in 1998 admitted the CIA ‘overlooked’ or ‘ignored’ reports that the Nicaragua Contra rebels financed their fight to oust the communist Sandinistas through the sale of drugs in the United States. **‘HIV-1’ is the form of ‘HIV’ allegedly most common and threatening to humans. According to the official tale, ‘HIV-2’ is rare and of little threat. Share https://substack.com/home/post/p-146567752
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    Why the Official AIDS Story is a Complete Crock
    The Great Rebranding, 1980s-Style: HIV Was a Sham, Just Like Sars-Cov-2
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  • EDTA Snakeoil! Ana Maria Mihalcea's Medical Malfeasance Exposed
    “I already have had.. uh.. patients die from shedding” - Ana Maria Mihalcea, M.D.

    Dr. Ariyana Love (ND)
    “My people are destroyed for lack of knowledge: because thou hast rejected knowledge, I will also reject thee, that thou shalt be no priest to me: seeing thou hast forgotten the law of thy God, I will also forget thy children.” ~ Hosea 4:6 KJV

    Rockefeller Medicine

    Around 1900, the science world was getting excited about new “petrochemicals” and the ability to create a variety of new compounds from oil. Some of the first products derived from petrochemicals were plastics.

    In 1908, modern medicine was established by the Rockefeller’s and dubbed “Allopathy”. The Rockefeller’s created the business of modern medicine which has always been about poisoning people, Eustice Mullen explains.

    This is the definition of Allopathic medicine according to the NIH:

    “A system in which medical doctors and other health care professionals (such as nurses, pharmacists, and therapists) treat symptoms and diseases using drugs, radiation, or surgery.”

    The Rockefeller Institute for Medicine, founded in 1908, marked the advent of the re-creation of synthetic versions of natural cures. Prior to 1908, every place of healing in America, Europe and the world, used only ancient traditional natural medicinal cures. Every hospital was a “Homeopathic Hospital”. Most of these magnificent buildings were converted into mental health asylums where a system of torture and electric shock was established to “cure” mental illness.


    John D. Rockefeller created the oil industry and used it to crush traditional medicine in order to enslave people. They also financed the Eugenics movement. One of the perks of modern medicine is depopulation.

    “Everyone knows that the infamous Roe v. Wade opinion legalized abortion, but almost no one knows that legal abortion was a strategy by eugenicists, as early as 1939, to “genetically improve” the population by “reducing” it.”

    In the book, “Rockefeller Medicine Men: Medicine and Capitalism in America”, authored by E. Richard Brown, he tells the hidden story of the financial, political, and institutional manipulations whereby a diverse and eclectic range of traditional healing modalities available to the North American public was summarily canceled and pared down to a singular style of medicine that would become the predominant medicine of the Western world and a major force in global medical culture during the 20th century. This was brought about largely by the collaboration of the American Medical Association, the philanthropies of Andrew Carnegie and John D. Rockefeller, and the development of a revolutionary curriculum by the Johns Hopkins School of Medicine. Brown documents the story of how a powerful professional elite gained virtual hegemony in the Western theatre of healing by effectively taking control of the ethos and practice of Western medicine. E. Richard Brown describes how, in 1905, the American Medical Association’s new Council on Medical Education funded by Carnegie and Rockefeller commenced serious activity. They employed the services of Abraham Flexner who proceeded to visit and “assess” every single medical school in the US and Canada. Within a short time of this development, medical schools all around the US began to collapse or consolidate. By 1910, 30 schools had merged, and 21 had closed their doors. Of the 166 medical schools operating in 1904, 133 had survived by 1910, and 104 by 1915. Fifteen years later, only 76 schools of medicine existed in the US and they all followed the same curriculum.

    The 1910 Flexner Report laid the foundations of the modern medical system, dubbed “Rockefeller medicine” (Allopathy). Since 1910, corporate interests have established near total control of the medical field, both though pharmacology and through their impact on medical education.

    In 1935, vitamin C became the first vitamin to be artificially synthesized in Switzerland. Rockefeller saw a big opportunity with the possibility that vitamins and medications could be developed from petroleum. He saw the chance to control and monopolize multiple industries at once: petroleum, chemical and medical. Petrochemicals were ideal from a business perspective because they could be patented, owned and sold for high profits.

    Today, the petrochemicals in plastics are causing a slew of illnesses including neurodevelopmental disorders, diabetes, chronic respiratory disease, and cancer, which have increased between 28% and 150% between 1990 and 2019. Petrochemicals in microplastics are also rapidly reducing fertility in males in particular, and polluting our environment. Please also read more here, here, and here.

    The first pharmaceutical drug was an arsenic named Salvarsan. That’s right, an ARSENIC!

    DEATH is an all-to-common side effect of pharmaceutical drugs which is only logical when you administer poisons internally. The following pages demonstrate the many deaths of people around the world, most of them children, who were fatally poisoned during the first mass medication experiments with Rockefeller’s Allopathic health. The paper is entitled, Toward Responsibility in International Health: Death following Treatment in Rockefeller Hookworm Campaigns, 1914–1934.

    What is EDTA?

    EDTA is synthesized on an industrial scale using 1, 2-diaminoethane (ethylene diamine), formaldehyde, water and sodium cyanide.

    Ethylene diamine induced acute and subchronic toxicity in lab animals, also allergic hypersensitivity. The liver and kidneys are target organs of ethylenediamine, where they simply stop working.


    Read more: Is C60 And EDTA Safe? Clinical Review


    Absorption of large amounts of formaldehyde via any route can cause severe systemic toxicity, leading to metabolic acidosis, tissue and organ damage, and coma, according to the CDC.

    Exposure to sodium cyanide can be rapidly fatal. It has whole-body (systemic) effects, particularly affecting those organ systems most sensitive to low oxygen levels: the central nervous system (brain), the cardiovascular system (heart and blood vessels), and the pulmonary system (lungs), according to the CDC.

    EDTA is an industrial poison. The textile industry required a chelating agent to remove calcium during textile processing and this led to the synthesis of polyamino-carboxylic acids, one of which was EDTA. A patent was filed for EDTA in Germany in 1935, for industrial chemical use. EDTA is a synthetic acid effectively used to clean boiler rooms in nuclear power plants. In 1945, Franz Munz obtained a US EDTA patent in 1945. In 1947, EDTA was approved by the US Food and Drug Administration (FDA) as a food additive in “low doses” because it’s a forever chemical and a preservative.

    There are two different types of EDTA approved by the U.S. FDA. In 1953, Edetate calcium disodium also known as Calcium EDTA (marketed under the trade name Calcium Disodium Versenate registered ) was approved for the treatment of lead poisoning. Three years later, in 1956, a related EDTA compound, Edetate disodium, was also approved for clinical use. This compound, also known as Disodium EDTA, has been marketed under the trade names Disotate (registered) and Endrate (registered). The essential difference between these two compounds is that Calcium EDTA's structure has an incorporated Ca super(2+) moiety while Disodium EDTA does not. The use of the latter compound, Disodium EDTA, has been associated with life-threatening and fatal hypocalcemia.

    EDTA trial DEATHS

    An EDTA trial (Sloth-Nielsen et al., 1981) on the possible antiatherogenic effect of EDTA with 6 patients, showed clinical signs of potentially lethal hypocalcemia from abnormally low calcium levels caused by EDTA.

    Another EDTA chelation human trial in 2003-2005 resulted in DEATHS due to hypocalcemia.

    A 2006 EDTA chelation trial also resulted in DEATHS due to hypocalcemia.

    There were several DEATHS reported from cardiac arrest due to lethal hypocalcemia in EDTA trials in 2006 and 2008 and (Brown, Willis, Omalu, & Leiker, 2006; Baxter & Krenzelok, 2008), from calcium deficiency inducing alterations in the brain, and osteoporosis, which causes the bones to become brittle.

    In 2008, a clinical trial with EDTA chelation on autistic children also proved fatal, resulting in DEATHS of children.

    A 2007 EDTA chelation study proved KIDNEY FAILURE in humans.

    Decades of clinical studies demonstrate that EDTA treatment is associated with severe, life-threatening adverse effects, as Science Direct explained in 2016.

    “It should be emphasized that EDTA treatment is associated with severe, life-threatening adverse effects.

    EDTA for cardiovascular disease DEBUNKED

    Many Allopathic specialists tried to popularize the use of EDTA for chelation, to no avail. In the 1980s, Richard Casdorph, a practicing cardiologist, claimed improvements in ejection fractions of the heart and in cerebral blood flow with EDTA chelation therapy in several articles. McDonagh, Rudolph, and Cheraskin published about 30 articles documenting various positive effects of EDTA chelation. This group wrote articles showing no problems with kidney function in patients treated with EDTA according to the published protocol. At the same time, conventional cardiologists wrote several editorials against EDTA chelation. So the American Medical Association called for studies to see if chelation worked. The American Board of Chelation Therapy in 1983 was formed to certify doctors who give the therapy. It was later called the American Board of Clinical Metal Toxicology. ACAM also certified doctors who took its workshop on chelation therapy and passed its written and oral examinations. The Great Lakes College of Clinical Medicine, later called the International College of Integrative Medicine (ICIM), was formed in 1983 to teach and do research on chelation and other integrative therapies. After complex negotiations, in the late 1980's Walter Reed Army Hospital agreed to do a randomized clinical trial on EDTA chelation therapy, but part way through the study it was suddenly discontinued for unknown reasons.

    However, in a paper by Seely, Wu, and Mills, (2005), a systematic review of published articles in this field was undertaken. The authors concluded that the best current available evidence did not support the therapeutic use of EDTA chelation therapy in the treatment of cardiovascular disease. Similar results have been reported in review papers by Shrihari, Roy, Prabhakaran, and Reddy (2006) and Crisponi et al. (2015).

    While a 2002 EDTA large randomized clinical trial “showed benefit”, smaller studies were inconsistent.

    In the 1990s, the Federal Trade Commission filed a complaint against ACAM for making a claim in a brochure that chelation was effective for vascular disease. ACAM submitted almost 100 articles in support of the claim, but the FTC insisted that a large randomized trial was required to make that claim. ACAM finally gave up after spending a million dollars in legal fees and signed a consent order saying they would not make such a claim anymore, based on the evidence at that time.

    In conclusion, our study shows that in a population of stable, largely asymptomatic coronary artery disease patients with prior myocardial infarction, use of EDTA chelation therapy did not produce a measurable change in health-related quality of life over 2 years of follow-up.

    A slew of other adverse events such as lacrimation, nasal congestion, mucocutaneous lesions, glycosuria, hypotension, and ECG abnormalities (DISEASE OF THE HEART AND LUNGS) have also been reported as well as allergic reactions (Wax, 2013) to EDTA. Prolonged treatment with calcium EDTA gives rise to depletion of magnesium and trace-metal depletion, the most marked being due to the excretion of zinc. Zinc depletion destroys your cells’ ability to absorb nutrients and leads to diabetes.

    A 2015 study entitled, Quality of Life Outcomes with a Disodium EDTA Chelation Regimen for Coronary Disease: Results from the TACT Randomized Trial concluded with this statement:

    “In conclusion, our study shows that in a population of stable, largely asymptomatic coronary artery disease patients with prior myocardial infarction, use of EDTA chelation therapy did not produce a measurable change in health-related quality of life over 2 years of follow-up.”

    Severe kidney damage from EDTA chelation therapy was reported in a (Nissel 1986) trial. In a very short period of time, EDTA causes kidneys to shut down in complete failure.

    A study from 2015 suggests EDTA chelation for myocardial infarction with “modest” benefits to cardio health. However, I would suggest that the moderate benefits of this study were due to the high doses of vitamin C administered.

    A 2017 study on EDTA chelation for atherosclerosis and Miocardial Infraction concluded:

    “Unsubstantiated claims of chelation therapy as an effective treatment of atherosclerosis should be avoided and patients made aware of the inadequate evidence for efficacy and potential adverse effects, especially the harm that can occur if used as a substitute for proven therapies.”

    In a 2018 EDTA trial it was concluded:

    “These results… are not sufficient to support the routine use of chelation therapy for treatment of patients who have had an MI (Miocardial Infraction)”.

    A study from 2023 entitled, Chelation Therapy Associated with Antioxidant Supplementation Can Decrease Oxidative Stress and Inflammation in Multiple Sclerosis: Preliminary Results proved a flop with two participants discontinuing their trial participation.

    EDTA for lead poisoning DEBUNKED

    EDTA has also been touted as a treatment for lead poisoning. Because of its adverse effects, calcium EDTA was replaced by DMSA in the treatment of lead poisoning (Aposhian et al., 1995) in 1995. CaEDTA has also been used for the treatment of cases with manganese toxicity, but the result was neurotoxic symptoms resembling PARKINSONISM (Andersen, 1999).

    A 2004 trial showed that EDTA actually REDISTRIBUTES LEAD TO THE BRAIN after acute or chronic lead exposure (Andersen, 2004).

    Another trial proved adverse effects in 5 patients receiving EDTA at an outpatient chelation clinic in 2002, and all patients experienced gastrointestinal and musculoskeletal symptoms.

    Oral exposure to EDTA (2002) had produced adverse reproductive and developmental effects in animals. EDTA did not make it past the animal or human trials, so why are medical doctors using it in humans?

    A 2002 EDTA trial was performed on humans as a test for “chelation” therapy by a chelation clinic, demonstrating adverse events in 5 out of 5 patients.

    Additionally, EDTA is a persistent organic pollutant (POP). In that case, each intake would only be partially excreted, while the remaining chemicals build up in the body and produce cell death. And long-term exposure to calcium disodium EDTA creates toxicity and kidney damage.

    EDTA Snakeoil Salesmen

    In March 2023, Ana Maria Mihalcea interviewed Dr. Michael Roth who claims that EDTA is a “synthetic amino acid related to vinegar.” Together they make a slew of medical claims that are not scientifically proven, such as that EDTA “detoxifies covid vaccine, heavy metals, graphene oxide, parasites, hydrogels, and nanoparticles”.

    The only scientific tool Ana Maria uses to back her claims is dark field microscopy. You cannot see nanoparticles with a dark field microscope. It takes a spectroscopy microscope to identify nanoparticles. Her medical claims are simply fabricated and unscientific lies.

    Ana Maria and Dr. Ross made additional unproven medical statements that “EDTA removes the effects of a heart attack, can bring back the elderly from senility and Alzheimer’s, reduces blood pressure, detoxifies several snake and spider venoms, lowers insulin, smooths skin and wrinkles, ” and a host of other laughable health claims that aren’t backed by anything.

    Incidentally, Dr. Ross is now dead.

    “Dr. Roth sadly passed away on March 11/2023”


    My sources informed me that Dr. Rashid Buttar was using EDTA. Given that he was already severely poisoned as Stew Peter’s reported, using EDTA Acid would have been enough to tip him over the edge and kill him.

    EDTA is not an approved pharmaceutical drug. It was Covid Emergency approved by the FDA under an Emergency Use Authorization (EUA), just like the modified RNA (modRNA) Covid-19 vaccine nanotechnology.

    The National Center for Complementary and Integrative Health (.gov) makes it clear that the use of EDTA chelation for heart disease has not been approved by the FDA.

    Ana Maria has been touting EDTA as an “antioxidant” when it is not. She even published to her Substack that EDTA is an “Antioxidant” when in fact it’s an acid poison and an oxidant. Many people saw it on her Substack before she removed it.

    I’ve had over a dozen clients come to me extremely sick from EDTA pills and EDTA IV infusion. Some told me they thought it was a natural substance due to Ana Maria’s false advertising and medical malfeasance. A Medical Doctor is licensed to know wether EDTA Acid is an oxidant poison or an antioxidant. Not knowing this and inducing the death of a patient is not an acceptable excuse. Ana Maria is criminally liable.


    EDTA is an oxidant when used internally. The studies that refer to EDTA as an “antioxidant” are in vitro lab studies, not in vivo (inside the body).

    EDTA is used to preserve cell specimens for chemistry lab work because it prevents blood coagulation and oxidation of cells in a petri dish where it’s used for diagnostic purposes. This is the kind of “antioxidant” the studies are referring to. But when you infuse EDTA Acid into the human body, it acts as an oxidant poison.

    EDTA also will not decoagulate the blood in vivo (inside the body). But I can see how people who cannot read peer-reviewed literature could be deceived and manipulated by snake oil salesmen.

    For example, a study entitled, “Comparative study of the antioxidant capability of EDTA and Irganox”. EDTA is a preservative used in laboratories to preserve cells for scientific lab research. EDTA prevents the oxidation of cells in a petri dish. Oxygen causes cells to deteriorate, but labs need them to last longer for research purposes. When used inside the human body (in vivo), it’s a different story. Then EDTA acts as an oxidant poison, not an antioxidant. So this has a very different meaning.

    One of the well documented and widely known adverse events from EDTA “chelation” is DEATH, according to Mount Sinai.

    Other serious side effects that have been reported include low blood sugar, diminished calcium levels, headache, nausea, dangerously low blood pressure, kidney failure, organ damage, irregular heartbeat, seizures, or even death.

    I have to wonder if Ana Maria Mihalcea is informing her patients that death is a potential adverse event to EDTA chelation? In a March 24, 2024, broadcast that Ana Maria released, at the 53:24 minute mark, she makes a chilling confession:

    “I already have had… uh… patients die from the shedding”

    How many of Ana Maria Mihalcea’s patients have been killed by her EDTA infusion protocol? I was horrified when I heard Ana Maria’s confession because I haven’t had any clients die from shedding! I’ve treated many people who were extremely sick from shedding, and I helped them all to detox effectively. Some clients came to me after several hospitalizations from extreme shedding but none of them died in my care! Nobody needs to die from shedding if they use an effective detox protocol.

    Between 1-2 years, Ana Maria has been claiming that EDTA detoxes graphene, dissolves graphene and chelates heavy metals, but experts such as Dr. Robert Young and Dr. Judy Mikovitz told me this is impossible.

    Ana Maria has gone so far as to produce a medical study with unscientific claims right in the title, “EDTA Chelation Dissolves the Artificial Intelligence Magnetic Hydrogel Weapon”. The study was also promoted by Health Canada. In her study, Ana Maria claims that EDTA can “detoxify the body even from Graphene”.

    EDTA is not a detox agent! Again, it’s an oxidant that degrades cells whereas genuine antioxidants repair cells.

    Ana Maria does in fact know about oxidant poisons. In an interview from December 2022, she referred to graphene as an oxidant. At least she’s correct about something.

    Saul Green, Ph.D., and Wallace I. Sampson, M.D. wrote in great detail about the Implausibility of EDTA Chelation Therapy, stating:

    “EDTA chelation effectiveness is implausible; (2) the preponderance of evidence shows ineffectiveness; and (3) EDTA augments oxidative reactions involving iron instead of inhibiting them, resulting in increased likelihood of production of oxygen free radicals rather than neutralization of them, as claimed.”

    EDTA a precurser to cellular transfection

    The Rockefeller Institue of Medicine has done clinical research on EDTA. One particular study entitled, Studies of Cell Deformity from 1967, shows that cells will degrade from EDTA exposure, which also induces “deformation” on their surfaces. The trial demonstrated that EDTA stops cellular synthesis of calcium. They learned that calcium is bound to anionic sites at the cell periphery, some of which are located at the cellular electrokinetic surface.

    Due to Rockefeller’s research, EDTA is now used in electrophoresis which is a laboratory technique used to separate DNA, RNA or protein molecules based on their size and electrical charge. An electric current is used to move the molecules through a gel or other matrix, according to the National Human Genome Research Institute.

    In agarose gel electrophoresis, EDTA is added for chelating the magnesium ions which are cofactors for DNA nucleases. Hence, activity of DNA nucleases that may be present is inhibited, and “DNA is protected from degrading”. This is why EDTA is an effective transfection agent because it dissolves parts of your DNA, preserving cells for lab research in vitro.

    Gel electrophoresis using EDTA is routinely used for detection and size analysis of proteins and nucleic acid. DMSO is used with EDTA in this process. This destruction of cells makes transfection (gene editing) of cells easier using CRISPR-Cas9 which splices and dices the genome in vivo, as this study explains entitled, “Inhibition of CRISPR-Cas9 ribonucleoprotein complex assembly by anti-CRISPR AcrIIC2”.


    EDTA was found to be genotoxic in laboratory animals. A study from 1983 demonstrates that EDTA induces gene mutations and chromosomal breakage, meaning that genetic mutations will be passed on your offspring, affecting generations to come, according to this Genetic Toxicology of EDTA study from 1983.

    Calcium chelate of EDTA (CaEDTA) “chelation” has shown teratogenic effects (Catsch & Harmuth-Hoene, 1976), which are central nervous system depression and peripheral neuropathy. EDTA produced abnormalities in pups of rats removed by cesarian section on day 21 of the study. Increases in several abnormalities (cleft palate, adactyly or syndactyly, abnormal rib or abnormal vertebrae) were observed with increased doses of CaEDTA.

    EDTA improves transfection of embryonic stem cells lines (hESC) in cells, according to the NIH.

    According to a peer reviewed paper from the NIH, EDTA is a precursor to cellular transfection.

    “We found that chemically abrading the differentiated CACO-2 human intestinal epithelial cell layer by a trypsin and EDTA pretreatment (before the use of detergent-like transfection reagents) dramatically improved transfection efficiency in this polar, differentiated model. Although this treatment did improve the transfection efficiency, it also induced leakiness in the epithelial barrier by both opening tight junctional complexes and by creating holes in the cell layer because of low-level cell death and detachment. Thus, this approach to enhance the transfection efficiency of polar, differentiated cells will be useful for assessment of the effect of the transfected/expressed protein on (re)formation of an epithelial barrier..."

    Thermo Fisher Scientific Inc. Fetal Bovine Serum for human transfection also uses EDTA.


    An NIH study entitled, “Kinetic Basis for DNA Target Specificity of CRISPR-Cas12a” reveals that EDTA enables rapid binding to DNA during gene editing (transfection).

    Another study entitled, “Improved genome editing by an engineered CRISPR-Cas12a” explains:

    “CAS12a is an RNA-guided, programmable genome editing enzyme found within bacterial adaptive immune pathways. Unlike CRISPR-Cas9, Cas12a uses only a single catalytic site to both cleave target double-stranded DNA (dsDNA) (cis-activity) and indiscriminately degrade single-stranded DNA (ssDNA) (trans-activity).”

    According to the study, “A DNA loading buffer of 45% formamide and 15 mM EDTA, with a trace amount of xylene cyanol and bromophenol blue…” is used to transfect the human genome.

    So, EDTA is a transfection agent used with CRISPR-Cas9 to edit the human genome. Does EDTA actually dissolve graphene, as Ana Maria claims? The answer is NO! EDTA oxidant is used to reduce graphene to Reduced Graphene Oxide (RGO) form. Graphene is reduced by oxidation. Rather than dissolving graphene, EDTA reduces it to Graphene Oxide Nanoparticles otherwise known as Quantum Dots.

    Graphene oxide is more toxic than graphene, as I documented in my article entitled, “Graphene Oxide The Vector For Covid-19 Democide”.

    I will emphasize again that Graphene Oxide Quantum Dots cannot be seen with a dark field microscope. So Ana Maria’s claims that EDTA is detoxing graphene from the human body is unscientific.

    EDTA chelation for graphene nanocomposites

    EDTA chelation is NOT effective in removing metals from the human body. It's actually a different kind of chelation that’s used to create electrochemical sensors (biosensors) when combined with GRAPHENE!

    EDTA serves as a connecting mediator between NiHCF (Graphene Oxide Nanoparticles and Nickle) and graphene nanosheets. EDTA is used with metal nanoparticles, metal oxides, graphene, carbon nanotubes, and quantum dots to stabilize the technology for a more uniform distribution throughout the body.

    A Science Direct paper entitled, “Highly sensitive ascorbid acid sensors from EDTA chelation derived nickel hexacyanoferrate/graphene nanocomposites” reveals that EDTA is used to create Graphene/Nickel, AA sensor nanocomposites.

    “EDTA chelation stragey” is used for the “homogeneously distrubuted" NiHCF” (Nickel hexacyanoferrate composite) on graphene sheets. EDTA residue-supported pyramidal and spherical nanoparticles of NiHCF deposited on graphene sheets is used to create biosensors for the formation of Graphene/Nickel hydrogels.


    The graphene hydrogel nanocomposite sensors (Gr/NiHCF) are used as externally controlled biosensing tools. They tell us it’s used to test for ascorbic acid, but the application of this technology is for “human life” as well as for industrial use. See link here.


    Graphene oxide/Lauric acid nanoparticles are modified using EDTA. Lauric acid nanoparticles is suggested as a “prospective drug carrier” for oral nanoparticle-mediated sustained drug delivery (timed release technology) used for the removal of Pb(II) ions (lead). However, studies show there are cytotoxic results.

    Another study entitled, “Improved genome editing by an engineered CRISPR-Cas12a” demonstrates how EDTA improves transfection and modification of the human genome.

    Once Graphene is reduced to Graphene Oxide, due to its small particulate size, you can no longer identify it using a Dark Field Microscope. Ana Maria is using a dark field scope, not a spectroscopy microscope, which is the only instrument that can measure GON and Quantum Dots.

    So what is Ana Maria doing with EDTA infusions? She’s creating a metal-EDTA complex that stabilizes and strengthens the graphene-based nanotech weapon system and enables it to spread more readily throughout the body, for human transfection. She uses “light and sound healing techniques” to activate the delayed release technology before administering EDTA infusion, as she reveals in an interview here.

    EDTA is a poison acid that dissolves DNA. It's used to prime the cells’ DNA for transfection. EDTA disrupts the surface of skin cells so that other chemicals can penetrate more easily and CRISPR-Cas9 gene editing technology can work more efficiently.

    The NIH describes EDTA’s enhanced cellular transfection:

    “Flow cytometric analysis using an enhanced green fluorescent protein vector showed a significantly increased transfection efficiency of EDTA method compared to standard enzyme method. In addition, the EDTA approach maintained stable cell viability and recovery rate of hESCs after transfection.”

    Another study published in Research Gate, confirms that EDTA increases cellular transfection, along with using chloroquine.

    Graphene Oxide Quantum Dots (GOQD-HA) nanocomposite use EDTA for tissue-specific delivery of Metformin, an anti-diabetic drug otherwise known as insulin.


    Conclusion

    Beware of snakeoil salesmen! Never trust pharmaceuticals! Superior heavy metal chelation supplements exist such as ASEA redox molecules and Master Peace, sign up and order here. Medicines made from nature are always superior to pharmaceutical drugs. Finally, be sure your Naturopathic Doctor is competent!

    Schedule a health consultation with me for a customized detox protocol and complete cellular health restoration.

    https://substack.com/home/post/p-144979143
    EDTA Snakeoil! Ana Maria Mihalcea's Medical Malfeasance Exposed “I already have had.. uh.. patients die from shedding” - Ana Maria Mihalcea, M.D. Dr. Ariyana Love (ND) “My people are destroyed for lack of knowledge: because thou hast rejected knowledge, I will also reject thee, that thou shalt be no priest to me: seeing thou hast forgotten the law of thy God, I will also forget thy children.” ~ Hosea 4:6 KJV Rockefeller Medicine Around 1900, the science world was getting excited about new “petrochemicals” and the ability to create a variety of new compounds from oil. Some of the first products derived from petrochemicals were plastics. In 1908, modern medicine was established by the Rockefeller’s and dubbed “Allopathy”. The Rockefeller’s created the business of modern medicine which has always been about poisoning people, Eustice Mullen explains. This is the definition of Allopathic medicine according to the NIH: “A system in which medical doctors and other health care professionals (such as nurses, pharmacists, and therapists) treat symptoms and diseases using drugs, radiation, or surgery.” The Rockefeller Institute for Medicine, founded in 1908, marked the advent of the re-creation of synthetic versions of natural cures. Prior to 1908, every place of healing in America, Europe and the world, used only ancient traditional natural medicinal cures. Every hospital was a “Homeopathic Hospital”. Most of these magnificent buildings were converted into mental health asylums where a system of torture and electric shock was established to “cure” mental illness. John D. Rockefeller created the oil industry and used it to crush traditional medicine in order to enslave people. They also financed the Eugenics movement. One of the perks of modern medicine is depopulation. “Everyone knows that the infamous Roe v. Wade opinion legalized abortion, but almost no one knows that legal abortion was a strategy by eugenicists, as early as 1939, to “genetically improve” the population by “reducing” it.” In the book, “Rockefeller Medicine Men: Medicine and Capitalism in America”, authored by E. Richard Brown, he tells the hidden story of the financial, political, and institutional manipulations whereby a diverse and eclectic range of traditional healing modalities available to the North American public was summarily canceled and pared down to a singular style of medicine that would become the predominant medicine of the Western world and a major force in global medical culture during the 20th century. This was brought about largely by the collaboration of the American Medical Association, the philanthropies of Andrew Carnegie and John D. Rockefeller, and the development of a revolutionary curriculum by the Johns Hopkins School of Medicine. Brown documents the story of how a powerful professional elite gained virtual hegemony in the Western theatre of healing by effectively taking control of the ethos and practice of Western medicine. E. Richard Brown describes how, in 1905, the American Medical Association’s new Council on Medical Education funded by Carnegie and Rockefeller commenced serious activity. They employed the services of Abraham Flexner who proceeded to visit and “assess” every single medical school in the US and Canada. Within a short time of this development, medical schools all around the US began to collapse or consolidate. By 1910, 30 schools had merged, and 21 had closed their doors. Of the 166 medical schools operating in 1904, 133 had survived by 1910, and 104 by 1915. Fifteen years later, only 76 schools of medicine existed in the US and they all followed the same curriculum. The 1910 Flexner Report laid the foundations of the modern medical system, dubbed “Rockefeller medicine” (Allopathy). Since 1910, corporate interests have established near total control of the medical field, both though pharmacology and through their impact on medical education. In 1935, vitamin C became the first vitamin to be artificially synthesized in Switzerland. Rockefeller saw a big opportunity with the possibility that vitamins and medications could be developed from petroleum. He saw the chance to control and monopolize multiple industries at once: petroleum, chemical and medical. Petrochemicals were ideal from a business perspective because they could be patented, owned and sold for high profits. Today, the petrochemicals in plastics are causing a slew of illnesses including neurodevelopmental disorders, diabetes, chronic respiratory disease, and cancer, which have increased between 28% and 150% between 1990 and 2019. Petrochemicals in microplastics are also rapidly reducing fertility in males in particular, and polluting our environment. Please also read more here, here, and here. The first pharmaceutical drug was an arsenic named Salvarsan. That’s right, an ARSENIC! DEATH is an all-to-common side effect of pharmaceutical drugs which is only logical when you administer poisons internally. The following pages demonstrate the many deaths of people around the world, most of them children, who were fatally poisoned during the first mass medication experiments with Rockefeller’s Allopathic health. The paper is entitled, Toward Responsibility in International Health: Death following Treatment in Rockefeller Hookworm Campaigns, 1914–1934. What is EDTA? EDTA is synthesized on an industrial scale using 1, 2-diaminoethane (ethylene diamine), formaldehyde, water and sodium cyanide. Ethylene diamine induced acute and subchronic toxicity in lab animals, also allergic hypersensitivity. The liver and kidneys are target organs of ethylenediamine, where they simply stop working. Read more: Is C60 And EDTA Safe? Clinical Review Absorption of large amounts of formaldehyde via any route can cause severe systemic toxicity, leading to metabolic acidosis, tissue and organ damage, and coma, according to the CDC. Exposure to sodium cyanide can be rapidly fatal. It has whole-body (systemic) effects, particularly affecting those organ systems most sensitive to low oxygen levels: the central nervous system (brain), the cardiovascular system (heart and blood vessels), and the pulmonary system (lungs), according to the CDC. EDTA is an industrial poison. The textile industry required a chelating agent to remove calcium during textile processing and this led to the synthesis of polyamino-carboxylic acids, one of which was EDTA. A patent was filed for EDTA in Germany in 1935, for industrial chemical use. EDTA is a synthetic acid effectively used to clean boiler rooms in nuclear power plants. In 1945, Franz Munz obtained a US EDTA patent in 1945. In 1947, EDTA was approved by the US Food and Drug Administration (FDA) as a food additive in “low doses” because it’s a forever chemical and a preservative. There are two different types of EDTA approved by the U.S. FDA. In 1953, Edetate calcium disodium also known as Calcium EDTA (marketed under the trade name Calcium Disodium Versenate registered ) was approved for the treatment of lead poisoning. Three years later, in 1956, a related EDTA compound, Edetate disodium, was also approved for clinical use. This compound, also known as Disodium EDTA, has been marketed under the trade names Disotate (registered) and Endrate (registered). The essential difference between these two compounds is that Calcium EDTA's structure has an incorporated Ca super(2+) moiety while Disodium EDTA does not. The use of the latter compound, Disodium EDTA, has been associated with life-threatening and fatal hypocalcemia. EDTA trial DEATHS An EDTA trial (Sloth-Nielsen et al., 1981) on the possible antiatherogenic effect of EDTA with 6 patients, showed clinical signs of potentially lethal hypocalcemia from abnormally low calcium levels caused by EDTA. Another EDTA chelation human trial in 2003-2005 resulted in DEATHS due to hypocalcemia. A 2006 EDTA chelation trial also resulted in DEATHS due to hypocalcemia. There were several DEATHS reported from cardiac arrest due to lethal hypocalcemia in EDTA trials in 2006 and 2008 and (Brown, Willis, Omalu, & Leiker, 2006; Baxter & Krenzelok, 2008), from calcium deficiency inducing alterations in the brain, and osteoporosis, which causes the bones to become brittle. In 2008, a clinical trial with EDTA chelation on autistic children also proved fatal, resulting in DEATHS of children. A 2007 EDTA chelation study proved KIDNEY FAILURE in humans. Decades of clinical studies demonstrate that EDTA treatment is associated with severe, life-threatening adverse effects, as Science Direct explained in 2016. “It should be emphasized that EDTA treatment is associated with severe, life-threatening adverse effects. EDTA for cardiovascular disease DEBUNKED Many Allopathic specialists tried to popularize the use of EDTA for chelation, to no avail. In the 1980s, Richard Casdorph, a practicing cardiologist, claimed improvements in ejection fractions of the heart and in cerebral blood flow with EDTA chelation therapy in several articles. McDonagh, Rudolph, and Cheraskin published about 30 articles documenting various positive effects of EDTA chelation. This group wrote articles showing no problems with kidney function in patients treated with EDTA according to the published protocol. At the same time, conventional cardiologists wrote several editorials against EDTA chelation. So the American Medical Association called for studies to see if chelation worked. The American Board of Chelation Therapy in 1983 was formed to certify doctors who give the therapy. It was later called the American Board of Clinical Metal Toxicology. ACAM also certified doctors who took its workshop on chelation therapy and passed its written and oral examinations. The Great Lakes College of Clinical Medicine, later called the International College of Integrative Medicine (ICIM), was formed in 1983 to teach and do research on chelation and other integrative therapies. After complex negotiations, in the late 1980's Walter Reed Army Hospital agreed to do a randomized clinical trial on EDTA chelation therapy, but part way through the study it was suddenly discontinued for unknown reasons. However, in a paper by Seely, Wu, and Mills, (2005), a systematic review of published articles in this field was undertaken. The authors concluded that the best current available evidence did not support the therapeutic use of EDTA chelation therapy in the treatment of cardiovascular disease. Similar results have been reported in review papers by Shrihari, Roy, Prabhakaran, and Reddy (2006) and Crisponi et al. (2015). While a 2002 EDTA large randomized clinical trial “showed benefit”, smaller studies were inconsistent. In the 1990s, the Federal Trade Commission filed a complaint against ACAM for making a claim in a brochure that chelation was effective for vascular disease. ACAM submitted almost 100 articles in support of the claim, but the FTC insisted that a large randomized trial was required to make that claim. ACAM finally gave up after spending a million dollars in legal fees and signed a consent order saying they would not make such a claim anymore, based on the evidence at that time. In conclusion, our study shows that in a population of stable, largely asymptomatic coronary artery disease patients with prior myocardial infarction, use of EDTA chelation therapy did not produce a measurable change in health-related quality of life over 2 years of follow-up. A slew of other adverse events such as lacrimation, nasal congestion, mucocutaneous lesions, glycosuria, hypotension, and ECG abnormalities (DISEASE OF THE HEART AND LUNGS) have also been reported as well as allergic reactions (Wax, 2013) to EDTA. Prolonged treatment with calcium EDTA gives rise to depletion of magnesium and trace-metal depletion, the most marked being due to the excretion of zinc. Zinc depletion destroys your cells’ ability to absorb nutrients and leads to diabetes. A 2015 study entitled, Quality of Life Outcomes with a Disodium EDTA Chelation Regimen for Coronary Disease: Results from the TACT Randomized Trial concluded with this statement: “In conclusion, our study shows that in a population of stable, largely asymptomatic coronary artery disease patients with prior myocardial infarction, use of EDTA chelation therapy did not produce a measurable change in health-related quality of life over 2 years of follow-up.” Severe kidney damage from EDTA chelation therapy was reported in a (Nissel 1986) trial. In a very short period of time, EDTA causes kidneys to shut down in complete failure. A study from 2015 suggests EDTA chelation for myocardial infarction with “modest” benefits to cardio health. However, I would suggest that the moderate benefits of this study were due to the high doses of vitamin C administered. A 2017 study on EDTA chelation for atherosclerosis and Miocardial Infraction concluded: “Unsubstantiated claims of chelation therapy as an effective treatment of atherosclerosis should be avoided and patients made aware of the inadequate evidence for efficacy and potential adverse effects, especially the harm that can occur if used as a substitute for proven therapies.” In a 2018 EDTA trial it was concluded: “These results… are not sufficient to support the routine use of chelation therapy for treatment of patients who have had an MI (Miocardial Infraction)”. A study from 2023 entitled, Chelation Therapy Associated with Antioxidant Supplementation Can Decrease Oxidative Stress and Inflammation in Multiple Sclerosis: Preliminary Results proved a flop with two participants discontinuing their trial participation. EDTA for lead poisoning DEBUNKED EDTA has also been touted as a treatment for lead poisoning. Because of its adverse effects, calcium EDTA was replaced by DMSA in the treatment of lead poisoning (Aposhian et al., 1995) in 1995. CaEDTA has also been used for the treatment of cases with manganese toxicity, but the result was neurotoxic symptoms resembling PARKINSONISM (Andersen, 1999). A 2004 trial showed that EDTA actually REDISTRIBUTES LEAD TO THE BRAIN after acute or chronic lead exposure (Andersen, 2004). Another trial proved adverse effects in 5 patients receiving EDTA at an outpatient chelation clinic in 2002, and all patients experienced gastrointestinal and musculoskeletal symptoms. Oral exposure to EDTA (2002) had produced adverse reproductive and developmental effects in animals. EDTA did not make it past the animal or human trials, so why are medical doctors using it in humans? A 2002 EDTA trial was performed on humans as a test for “chelation” therapy by a chelation clinic, demonstrating adverse events in 5 out of 5 patients. Additionally, EDTA is a persistent organic pollutant (POP). In that case, each intake would only be partially excreted, while the remaining chemicals build up in the body and produce cell death. And long-term exposure to calcium disodium EDTA creates toxicity and kidney damage. EDTA Snakeoil Salesmen In March 2023, Ana Maria Mihalcea interviewed Dr. Michael Roth who claims that EDTA is a “synthetic amino acid related to vinegar.” Together they make a slew of medical claims that are not scientifically proven, such as that EDTA “detoxifies covid vaccine, heavy metals, graphene oxide, parasites, hydrogels, and nanoparticles”. The only scientific tool Ana Maria uses to back her claims is dark field microscopy. You cannot see nanoparticles with a dark field microscope. It takes a spectroscopy microscope to identify nanoparticles. Her medical claims are simply fabricated and unscientific lies. Ana Maria and Dr. Ross made additional unproven medical statements that “EDTA removes the effects of a heart attack, can bring back the elderly from senility and Alzheimer’s, reduces blood pressure, detoxifies several snake and spider venoms, lowers insulin, smooths skin and wrinkles, ” and a host of other laughable health claims that aren’t backed by anything. Incidentally, Dr. Ross is now dead. “Dr. Roth sadly passed away on March 11/2023” My sources informed me that Dr. Rashid Buttar was using EDTA. Given that he was already severely poisoned as Stew Peter’s reported, using EDTA Acid would have been enough to tip him over the edge and kill him. EDTA is not an approved pharmaceutical drug. It was Covid Emergency approved by the FDA under an Emergency Use Authorization (EUA), just like the modified RNA (modRNA) Covid-19 vaccine nanotechnology. The National Center for Complementary and Integrative Health (.gov) makes it clear that the use of EDTA chelation for heart disease has not been approved by the FDA. Ana Maria has been touting EDTA as an “antioxidant” when it is not. She even published to her Substack that EDTA is an “Antioxidant” when in fact it’s an acid poison and an oxidant. Many people saw it on her Substack before she removed it. I’ve had over a dozen clients come to me extremely sick from EDTA pills and EDTA IV infusion. Some told me they thought it was a natural substance due to Ana Maria’s false advertising and medical malfeasance. A Medical Doctor is licensed to know wether EDTA Acid is an oxidant poison or an antioxidant. Not knowing this and inducing the death of a patient is not an acceptable excuse. Ana Maria is criminally liable. EDTA is an oxidant when used internally. The studies that refer to EDTA as an “antioxidant” are in vitro lab studies, not in vivo (inside the body). EDTA is used to preserve cell specimens for chemistry lab work because it prevents blood coagulation and oxidation of cells in a petri dish where it’s used for diagnostic purposes. This is the kind of “antioxidant” the studies are referring to. But when you infuse EDTA Acid into the human body, it acts as an oxidant poison. EDTA also will not decoagulate the blood in vivo (inside the body). But I can see how people who cannot read peer-reviewed literature could be deceived and manipulated by snake oil salesmen. For example, a study entitled, “Comparative study of the antioxidant capability of EDTA and Irganox”. EDTA is a preservative used in laboratories to preserve cells for scientific lab research. EDTA prevents the oxidation of cells in a petri dish. Oxygen causes cells to deteriorate, but labs need them to last longer for research purposes. When used inside the human body (in vivo), it’s a different story. Then EDTA acts as an oxidant poison, not an antioxidant. So this has a very different meaning. One of the well documented and widely known adverse events from EDTA “chelation” is DEATH, according to Mount Sinai. Other serious side effects that have been reported include low blood sugar, diminished calcium levels, headache, nausea, dangerously low blood pressure, kidney failure, organ damage, irregular heartbeat, seizures, or even death. I have to wonder if Ana Maria Mihalcea is informing her patients that death is a potential adverse event to EDTA chelation? In a March 24, 2024, broadcast that Ana Maria released, at the 53:24 minute mark, she makes a chilling confession: “I already have had… uh… patients die from the shedding” How many of Ana Maria Mihalcea’s patients have been killed by her EDTA infusion protocol? I was horrified when I heard Ana Maria’s confession because I haven’t had any clients die from shedding! I’ve treated many people who were extremely sick from shedding, and I helped them all to detox effectively. Some clients came to me after several hospitalizations from extreme shedding but none of them died in my care! Nobody needs to die from shedding if they use an effective detox protocol. Between 1-2 years, Ana Maria has been claiming that EDTA detoxes graphene, dissolves graphene and chelates heavy metals, but experts such as Dr. Robert Young and Dr. Judy Mikovitz told me this is impossible. Ana Maria has gone so far as to produce a medical study with unscientific claims right in the title, “EDTA Chelation Dissolves the Artificial Intelligence Magnetic Hydrogel Weapon”. The study was also promoted by Health Canada. In her study, Ana Maria claims that EDTA can “detoxify the body even from Graphene”. EDTA is not a detox agent! Again, it’s an oxidant that degrades cells whereas genuine antioxidants repair cells. Ana Maria does in fact know about oxidant poisons. In an interview from December 2022, she referred to graphene as an oxidant. At least she’s correct about something. Saul Green, Ph.D., and Wallace I. Sampson, M.D. wrote in great detail about the Implausibility of EDTA Chelation Therapy, stating: “EDTA chelation effectiveness is implausible; (2) the preponderance of evidence shows ineffectiveness; and (3) EDTA augments oxidative reactions involving iron instead of inhibiting them, resulting in increased likelihood of production of oxygen free radicals rather than neutralization of them, as claimed.” EDTA a precurser to cellular transfection The Rockefeller Institue of Medicine has done clinical research on EDTA. One particular study entitled, Studies of Cell Deformity from 1967, shows that cells will degrade from EDTA exposure, which also induces “deformation” on their surfaces. The trial demonstrated that EDTA stops cellular synthesis of calcium. They learned that calcium is bound to anionic sites at the cell periphery, some of which are located at the cellular electrokinetic surface. Due to Rockefeller’s research, EDTA is now used in electrophoresis which is a laboratory technique used to separate DNA, RNA or protein molecules based on their size and electrical charge. An electric current is used to move the molecules through a gel or other matrix, according to the National Human Genome Research Institute. In agarose gel electrophoresis, EDTA is added for chelating the magnesium ions which are cofactors for DNA nucleases. Hence, activity of DNA nucleases that may be present is inhibited, and “DNA is protected from degrading”. This is why EDTA is an effective transfection agent because it dissolves parts of your DNA, preserving cells for lab research in vitro. Gel electrophoresis using EDTA is routinely used for detection and size analysis of proteins and nucleic acid. DMSO is used with EDTA in this process. This destruction of cells makes transfection (gene editing) of cells easier using CRISPR-Cas9 which splices and dices the genome in vivo, as this study explains entitled, “Inhibition of CRISPR-Cas9 ribonucleoprotein complex assembly by anti-CRISPR AcrIIC2”. EDTA was found to be genotoxic in laboratory animals. A study from 1983 demonstrates that EDTA induces gene mutations and chromosomal breakage, meaning that genetic mutations will be passed on your offspring, affecting generations to come, according to this Genetic Toxicology of EDTA study from 1983. Calcium chelate of EDTA (CaEDTA) “chelation” has shown teratogenic effects (Catsch & Harmuth-Hoene, 1976), which are central nervous system depression and peripheral neuropathy. EDTA produced abnormalities in pups of rats removed by cesarian section on day 21 of the study. Increases in several abnormalities (cleft palate, adactyly or syndactyly, abnormal rib or abnormal vertebrae) were observed with increased doses of CaEDTA. EDTA improves transfection of embryonic stem cells lines (hESC) in cells, according to the NIH. According to a peer reviewed paper from the NIH, EDTA is a precursor to cellular transfection. “We found that chemically abrading the differentiated CACO-2 human intestinal epithelial cell layer by a trypsin and EDTA pretreatment (before the use of detergent-like transfection reagents) dramatically improved transfection efficiency in this polar, differentiated model. Although this treatment did improve the transfection efficiency, it also induced leakiness in the epithelial barrier by both opening tight junctional complexes and by creating holes in the cell layer because of low-level cell death and detachment. Thus, this approach to enhance the transfection efficiency of polar, differentiated cells will be useful for assessment of the effect of the transfected/expressed protein on (re)formation of an epithelial barrier..." Thermo Fisher Scientific Inc. Fetal Bovine Serum for human transfection also uses EDTA. An NIH study entitled, “Kinetic Basis for DNA Target Specificity of CRISPR-Cas12a” reveals that EDTA enables rapid binding to DNA during gene editing (transfection). Another study entitled, “Improved genome editing by an engineered CRISPR-Cas12a” explains: “CAS12a is an RNA-guided, programmable genome editing enzyme found within bacterial adaptive immune pathways. Unlike CRISPR-Cas9, Cas12a uses only a single catalytic site to both cleave target double-stranded DNA (dsDNA) (cis-activity) and indiscriminately degrade single-stranded DNA (ssDNA) (trans-activity).” According to the study, “A DNA loading buffer of 45% formamide and 15 mM EDTA, with a trace amount of xylene cyanol and bromophenol blue…” is used to transfect the human genome. So, EDTA is a transfection agent used with CRISPR-Cas9 to edit the human genome. Does EDTA actually dissolve graphene, as Ana Maria claims? The answer is NO! EDTA oxidant is used to reduce graphene to Reduced Graphene Oxide (RGO) form. Graphene is reduced by oxidation. Rather than dissolving graphene, EDTA reduces it to Graphene Oxide Nanoparticles otherwise known as Quantum Dots. Graphene oxide is more toxic than graphene, as I documented in my article entitled, “Graphene Oxide The Vector For Covid-19 Democide”. I will emphasize again that Graphene Oxide Quantum Dots cannot be seen with a dark field microscope. So Ana Maria’s claims that EDTA is detoxing graphene from the human body is unscientific. EDTA chelation for graphene nanocomposites EDTA chelation is NOT effective in removing metals from the human body. It's actually a different kind of chelation that’s used to create electrochemical sensors (biosensors) when combined with GRAPHENE! EDTA serves as a connecting mediator between NiHCF (Graphene Oxide Nanoparticles and Nickle) and graphene nanosheets. EDTA is used with metal nanoparticles, metal oxides, graphene, carbon nanotubes, and quantum dots to stabilize the technology for a more uniform distribution throughout the body. A Science Direct paper entitled, “Highly sensitive ascorbid acid sensors from EDTA chelation derived nickel hexacyanoferrate/graphene nanocomposites” reveals that EDTA is used to create Graphene/Nickel, AA sensor nanocomposites. “EDTA chelation stragey” is used for the “homogeneously distrubuted" NiHCF” (Nickel hexacyanoferrate composite) on graphene sheets. EDTA residue-supported pyramidal and spherical nanoparticles of NiHCF deposited on graphene sheets is used to create biosensors for the formation of Graphene/Nickel hydrogels. The graphene hydrogel nanocomposite sensors (Gr/NiHCF) are used as externally controlled biosensing tools. They tell us it’s used to test for ascorbic acid, but the application of this technology is for “human life” as well as for industrial use. See link here. Graphene oxide/Lauric acid nanoparticles are modified using EDTA. Lauric acid nanoparticles is suggested as a “prospective drug carrier” for oral nanoparticle-mediated sustained drug delivery (timed release technology) used for the removal of Pb(II) ions (lead). However, studies show there are cytotoxic results. Another study entitled, “Improved genome editing by an engineered CRISPR-Cas12a” demonstrates how EDTA improves transfection and modification of the human genome. Once Graphene is reduced to Graphene Oxide, due to its small particulate size, you can no longer identify it using a Dark Field Microscope. Ana Maria is using a dark field scope, not a spectroscopy microscope, which is the only instrument that can measure GON and Quantum Dots. So what is Ana Maria doing with EDTA infusions? She’s creating a metal-EDTA complex that stabilizes and strengthens the graphene-based nanotech weapon system and enables it to spread more readily throughout the body, for human transfection. She uses “light and sound healing techniques” to activate the delayed release technology before administering EDTA infusion, as she reveals in an interview here. EDTA is a poison acid that dissolves DNA. It's used to prime the cells’ DNA for transfection. EDTA disrupts the surface of skin cells so that other chemicals can penetrate more easily and CRISPR-Cas9 gene editing technology can work more efficiently. The NIH describes EDTA’s enhanced cellular transfection: “Flow cytometric analysis using an enhanced green fluorescent protein vector showed a significantly increased transfection efficiency of EDTA method compared to standard enzyme method. In addition, the EDTA approach maintained stable cell viability and recovery rate of hESCs after transfection.” Another study published in Research Gate, confirms that EDTA increases cellular transfection, along with using chloroquine. Graphene Oxide Quantum Dots (GOQD-HA) nanocomposite use EDTA for tissue-specific delivery of Metformin, an anti-diabetic drug otherwise known as insulin. Conclusion Beware of snakeoil salesmen! Never trust pharmaceuticals! Superior heavy metal chelation supplements exist such as ASEA redox molecules and Master Peace, sign up and order here. Medicines made from nature are always superior to pharmaceutical drugs. Finally, be sure your Naturopathic Doctor is competent! Schedule a health consultation with me for a customized detox protocol and complete cellular health restoration. https://substack.com/home/post/p-144979143
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    EDTA Snakeoil! Ana Maria Mihalcea's Medical Malfeasance Exposed
    “I already have had.. uh.. patients die from shedding” - Ana Maria Mihalcea, M.D.
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  • Ana Maria Mihalcea's Defamation Against ASEA Redox Molecules
    Dr. Ariyana Love (ND)
    I met Ana Maria Mihalcea while I was working in Spain, in July 2022. I was meeting weekly with the Medical Doctors For Covid Ethics (MD4CE) group since October 2021. Ana Maria was invited into MD4CE group in the summer of 2022.

    Ana Maria learned from others in the MD4CE group that I was successfully detoxing people from the Covid-19 vaccines. She approached me early in July and asked me to do a Skype call with her. During the video call she told me that she’s a “Medical Doctor who now uses only Naturopathic Medicines”. She did this in order to get me to trust her but it’s obviously a lie because now she’s promoting unapproved industrial poisons such as EDTA and Methylene Blue.

    Ana Maria showed me two images that were supposedly of her own blood, and said that she had been “poisoned”. The blood image was clearly contaminated with Covid-19 tech. Ana Maria claimed that the tech induced brain injury and caused her to lose some of her cognitive ability. I could see the brain damage from the way she slurred her words and struggled to find words.

    Ana Maria told me she’d “tried everything to get the tech out” of her body but nothing worked, and she asked me if I could help her. I gave her a free consultation and instructed her to use 16 ounces of ASEA Redox daily, along with other supplements in my protocol. She further asked me if there was anything else that could be used to detox besides the Redox supplement. I told her that Humic Acid might work or at least it would help, along with other natural medicines in my protocol. I also told her that Humic Acid is natural nano-minerals so it’s aborption rate into cells is rapid, and it works as a cellular driver of nutrients.

    After the free consultation, Ana Maria began buying about 4 cases of the ASEA Redox supplement from me each month. Her first purchase was on July 10th 2022. She continued to buy 4 cases of the Redox supplement for 5 consecutive months.

    In September 2022, Ana Maria began telling people in the MD4CE group that redox molecules do not work. Despite this, she continued buying 4 cases per month from me.

    In October 2022, Ana Maria publicly addressed the MD4CE group on a weekly call with about 100 of the world’s leading experts in attendance, exclaiming that “ASEA Redox doesn’t work Ariyana”. I was stunned. That was a bald-faced lie!

    Ana Maria continued to purchase 4 cases of ASEA Redox in November 2022. Her last purchase was on December 27th, 2022. So, while Ana Maria was defaming me and ASEA to my colleagues and peers, she was simultaneously using my protocol to detox herself. Then she turned around and gave credit to EDTA. How bloody devious!

    The MD4CE group includes some of the world’s leading experts in the fields of medicine, science, biology, chemistry, and more. Ana Maria’s defamation resulted in members of the group lashing out at me, abusing me and putting me down. Despite the fact that the group is led by medical experts, they failed to do any due diligence and failed to read from the hundreds of thousands of peer-reviewed papers on the healing power of redox molecules, before inflicting damaging to my career.

    Ana Maria further stole my research and began using Humic Acid in her protocols with her patients! She did this without crediting me because she obviously felt entitled to do so.

    After Ana Maria lied about me and the efficacy of redox molecules to the medical doctors, the founder of the group, Dr. Stephen Frost, began censoring and defaming me as well. He and the moderator, Charles (CK), decided that I would no longer be allowed to speak in the group, despite that I’d been speaking freely in the group for an entire year, without any problems.

    I captured this screenshot on October 13, 2022, while I was in a MD4CE call when residing in Hollola, Finland.


    Dr. Stephen Frost contacted me in October 2021, asking me to join and give a presentation to the MD4CE group. I was in the group for several months before Charles joined and began moderating. Prior to Charles joining, the group operated democratically, and each member could raise their hand and have a turn at speaking and asking questions of other presenters.

    Treating me in this way and censoring my ability to interact in the group was degrading and hurtful. I took a screenshot of their undemocratic abuse and posted it onto the group chat for everyone to see. I wanted the others to know that I was being targeted. Immediately, Charles and Stephen removed me from the group and stopped sending me invites.

    Right before I was removed from MD4CE, I invited Dr. Robert Young into the group in October 2022. Despite that Dr. Young had analyzed ASEA’s redox molecules in a science lab and knew their efficacy, the medical doctors took Ana Maria’s word without question. Dr. Frost did not bother to consult with Dr. Young. He failed to read the research papers such as “ASEA And The Big Three” which demonstrates how redox molecules boost glutathione levels up to between 500-800%.


    Dr. Frost proceeded to defame me. I had a couple members of MD4CE reach out to tell me that Dr. Frost refused to give them my contact information when they asked him for it and told me he was attacking my good character.

    The Israeli-Zionists in MD4CE had also been pressuring Dr. Frost to remove me from the group ever since I joined. They attacked everyone who was exposing Graphene Oxide Nanoparticles in the Covid-19 jabs, including Karen Kingston and La Quinta Columna.

    MD4CE knowledge of redox molecules and our body’s natural operating system is close to non-existent. A few members were complaining that the Redox supplement was “too expensive”. They didn’t want ASEA to get the credit they deserve, possibly because it’s from nature and not a pharmaceutical. Instead of researching redox molecules, they chose to cancel me and inflict harm on my career. Dr. Frost has made no effort to apologize to me. He too feels entitled to discriminate against me.

    Ana Maria’s defamation was successful, but it didn’t stop there. She went straight to Stew Peters and got me canceled from his show with her viscous lies. My last interview with Stew Peters was a year ago, where I revealed that the patent for the PCR “test” is linked to human cloning. The interview was in September 2022.

    Dr. Judy Mikovitz went on the Thrivetime Show on InfoWars, and backed my research. Clay Clark played a clip of that interview with Stew Peters and asked Dr. Judy Mikovitz to comment on the PCR swabs being cloning devices. She not only backed my research, but she also revealed that SARS-Cov-2 is a “synthetic retrovirus" which is part of HIV and XRV (snake venom syncytin). It was a great interview that was unfortuneately censored!

    While many have heralded Ana Maria Mihalcea as a hero for mainstreaming a deadly industrial poison as a “detox” for Covid-19 vaccine injuries, and touting it as a miracle treatment for everybody else, it’s important to take a closer look at her shady character.

    Ana Maria is deeply involved in Ramtha’s teachings. Ramtha is a male entity channeled by a woman. Ana Maria’s testimonial was featured on Ramtha’s RSE Newsletter in 2014, where she boasts about Ramtha’s spiritual guidance enabling her to win more money by gambling on slot machines in a casino.

    In Ana Maria’s own words:

    “This past week, after a days work, and maintaining my Peace, I won:

    9/2/14 $1,300 Net on Rainbow Riches
    9//3/14 $1,715.75 Jackpot on Cheetah (Net $1,520)
    9/4/14 $700 Net on Cheetah
    9/5/14 $750 Net on Rainbow Riches
    9/7/14 $1,973 Jackpot on Count Vampire (Net $1,898)

    I went to the Casino on 9/6. I for the first time in days got angry about something at work and did not immediately self correct. I won that evening, but did not walk out with a net Win. That was a great lesson that Nothing and Nobody is worth loosing my Peace for and interrupting my future Consciousness Stream.”



    Now, are these spiritual values? I hope this sheds more light into Ana Maria’s ambitions.

    The MD4CE complained many times to me that ASEA Redox is “too expensive” but the EDTA chelation is about $2,000 per visit, not including travel! Whereas a case of ASEA Redox is $160 at retail price, and $130 wholesale, with a monthly subscription.

    ASEA Redox is perhaps the world’s most effective heavy metal chelator and this is why Ana Maria defamed me after using my protocol to detox herself while giving credit to EDTA “chelation”. She knows redox molecules are effective, but she had an agenda to get rich and sell EDTA snakeoil poison to people.

    Now Ana Maria is attacking Master Peace through a nurse practitioner. They’re falsely claiming that Master Peace includes self-assembling nanotechnology in an insidious attempt to defame the company and prevent people from achieving true detox. Ana Maria is defaming all the best supplements that are in competition with her EDTA snakeoil.

    Master Peace is another critical breakthrough in medicine. It’s affordable for all and is one of the best heavy metal chelators to exist. It works synergistically with redox molecules, increasing their efficacy.

    Please review the detailed peer reviewed literature on redox molecules and review the Dark Field Microscopy images of blood before and after using ASEA Redox, through the work of a colleague, Dr. Peggy Marienfeld.


    PLEASE READ: EDTA Snakeoil! Ana Maria Mihalcea’s Medical Malfeasance Exposed



    https://substack.com/home/post/p-144981224
    Ana Maria Mihalcea's Defamation Against ASEA Redox Molecules Dr. Ariyana Love (ND) I met Ana Maria Mihalcea while I was working in Spain, in July 2022. I was meeting weekly with the Medical Doctors For Covid Ethics (MD4CE) group since October 2021. Ana Maria was invited into MD4CE group in the summer of 2022. Ana Maria learned from others in the MD4CE group that I was successfully detoxing people from the Covid-19 vaccines. She approached me early in July and asked me to do a Skype call with her. During the video call she told me that she’s a “Medical Doctor who now uses only Naturopathic Medicines”. She did this in order to get me to trust her but it’s obviously a lie because now she’s promoting unapproved industrial poisons such as EDTA and Methylene Blue. Ana Maria showed me two images that were supposedly of her own blood, and said that she had been “poisoned”. The blood image was clearly contaminated with Covid-19 tech. Ana Maria claimed that the tech induced brain injury and caused her to lose some of her cognitive ability. I could see the brain damage from the way she slurred her words and struggled to find words. Ana Maria told me she’d “tried everything to get the tech out” of her body but nothing worked, and she asked me if I could help her. I gave her a free consultation and instructed her to use 16 ounces of ASEA Redox daily, along with other supplements in my protocol. She further asked me if there was anything else that could be used to detox besides the Redox supplement. I told her that Humic Acid might work or at least it would help, along with other natural medicines in my protocol. I also told her that Humic Acid is natural nano-minerals so it’s aborption rate into cells is rapid, and it works as a cellular driver of nutrients. After the free consultation, Ana Maria began buying about 4 cases of the ASEA Redox supplement from me each month. Her first purchase was on July 10th 2022. She continued to buy 4 cases of the Redox supplement for 5 consecutive months. In September 2022, Ana Maria began telling people in the MD4CE group that redox molecules do not work. Despite this, she continued buying 4 cases per month from me. In October 2022, Ana Maria publicly addressed the MD4CE group on a weekly call with about 100 of the world’s leading experts in attendance, exclaiming that “ASEA Redox doesn’t work Ariyana”. I was stunned. That was a bald-faced lie! Ana Maria continued to purchase 4 cases of ASEA Redox in November 2022. Her last purchase was on December 27th, 2022. So, while Ana Maria was defaming me and ASEA to my colleagues and peers, she was simultaneously using my protocol to detox herself. Then she turned around and gave credit to EDTA. How bloody devious! The MD4CE group includes some of the world’s leading experts in the fields of medicine, science, biology, chemistry, and more. Ana Maria’s defamation resulted in members of the group lashing out at me, abusing me and putting me down. Despite the fact that the group is led by medical experts, they failed to do any due diligence and failed to read from the hundreds of thousands of peer-reviewed papers on the healing power of redox molecules, before inflicting damaging to my career. Ana Maria further stole my research and began using Humic Acid in her protocols with her patients! She did this without crediting me because she obviously felt entitled to do so. After Ana Maria lied about me and the efficacy of redox molecules to the medical doctors, the founder of the group, Dr. Stephen Frost, began censoring and defaming me as well. He and the moderator, Charles (CK), decided that I would no longer be allowed to speak in the group, despite that I’d been speaking freely in the group for an entire year, without any problems. I captured this screenshot on October 13, 2022, while I was in a MD4CE call when residing in Hollola, Finland. Dr. Stephen Frost contacted me in October 2021, asking me to join and give a presentation to the MD4CE group. I was in the group for several months before Charles joined and began moderating. Prior to Charles joining, the group operated democratically, and each member could raise their hand and have a turn at speaking and asking questions of other presenters. Treating me in this way and censoring my ability to interact in the group was degrading and hurtful. I took a screenshot of their undemocratic abuse and posted it onto the group chat for everyone to see. I wanted the others to know that I was being targeted. Immediately, Charles and Stephen removed me from the group and stopped sending me invites. Right before I was removed from MD4CE, I invited Dr. Robert Young into the group in October 2022. Despite that Dr. Young had analyzed ASEA’s redox molecules in a science lab and knew their efficacy, the medical doctors took Ana Maria’s word without question. Dr. Frost did not bother to consult with Dr. Young. He failed to read the research papers such as “ASEA And The Big Three” which demonstrates how redox molecules boost glutathione levels up to between 500-800%. Dr. Frost proceeded to defame me. I had a couple members of MD4CE reach out to tell me that Dr. Frost refused to give them my contact information when they asked him for it and told me he was attacking my good character. The Israeli-Zionists in MD4CE had also been pressuring Dr. Frost to remove me from the group ever since I joined. They attacked everyone who was exposing Graphene Oxide Nanoparticles in the Covid-19 jabs, including Karen Kingston and La Quinta Columna. MD4CE knowledge of redox molecules and our body’s natural operating system is close to non-existent. A few members were complaining that the Redox supplement was “too expensive”. They didn’t want ASEA to get the credit they deserve, possibly because it’s from nature and not a pharmaceutical. Instead of researching redox molecules, they chose to cancel me and inflict harm on my career. Dr. Frost has made no effort to apologize to me. He too feels entitled to discriminate against me. Ana Maria’s defamation was successful, but it didn’t stop there. She went straight to Stew Peters and got me canceled from his show with her viscous lies. My last interview with Stew Peters was a year ago, where I revealed that the patent for the PCR “test” is linked to human cloning. The interview was in September 2022. Dr. Judy Mikovitz went on the Thrivetime Show on InfoWars, and backed my research. Clay Clark played a clip of that interview with Stew Peters and asked Dr. Judy Mikovitz to comment on the PCR swabs being cloning devices. She not only backed my research, but she also revealed that SARS-Cov-2 is a “synthetic retrovirus" which is part of HIV and XRV (snake venom syncytin). It was a great interview that was unfortuneately censored! While many have heralded Ana Maria Mihalcea as a hero for mainstreaming a deadly industrial poison as a “detox” for Covid-19 vaccine injuries, and touting it as a miracle treatment for everybody else, it’s important to take a closer look at her shady character. Ana Maria is deeply involved in Ramtha’s teachings. Ramtha is a male entity channeled by a woman. Ana Maria’s testimonial was featured on Ramtha’s RSE Newsletter in 2014, where she boasts about Ramtha’s spiritual guidance enabling her to win more money by gambling on slot machines in a casino. In Ana Maria’s own words: “This past week, after a days work, and maintaining my Peace, I won: 9/2/14 $1,300 Net on Rainbow Riches 9//3/14 $1,715.75 Jackpot on Cheetah (Net $1,520) 9/4/14 $700 Net on Cheetah 9/5/14 $750 Net on Rainbow Riches 9/7/14 $1,973 Jackpot on Count Vampire (Net $1,898) I went to the Casino on 9/6. I for the first time in days got angry about something at work and did not immediately self correct. I won that evening, but did not walk out with a net Win. That was a great lesson that Nothing and Nobody is worth loosing my Peace for and interrupting my future Consciousness Stream.” Now, are these spiritual values? I hope this sheds more light into Ana Maria’s ambitions. The MD4CE complained many times to me that ASEA Redox is “too expensive” but the EDTA chelation is about $2,000 per visit, not including travel! Whereas a case of ASEA Redox is $160 at retail price, and $130 wholesale, with a monthly subscription. ASEA Redox is perhaps the world’s most effective heavy metal chelator and this is why Ana Maria defamed me after using my protocol to detox herself while giving credit to EDTA “chelation”. She knows redox molecules are effective, but she had an agenda to get rich and sell EDTA snakeoil poison to people. Now Ana Maria is attacking Master Peace through a nurse practitioner. They’re falsely claiming that Master Peace includes self-assembling nanotechnology in an insidious attempt to defame the company and prevent people from achieving true detox. Ana Maria is defaming all the best supplements that are in competition with her EDTA snakeoil. Master Peace is another critical breakthrough in medicine. It’s affordable for all and is one of the best heavy metal chelators to exist. It works synergistically with redox molecules, increasing their efficacy. Please review the detailed peer reviewed literature on redox molecules and review the Dark Field Microscopy images of blood before and after using ASEA Redox, through the work of a colleague, Dr. Peggy Marienfeld. PLEASE READ: EDTA Snakeoil! Ana Maria Mihalcea’s Medical Malfeasance Exposed https://substack.com/home/post/p-144981224
    SUBSTACK.COM
    Ana Maria Mihalcea's Defamation Against ASEA Redox Molecules
    I met Ana Maria Mihalcea while I was working in Spain, in July 2022. I was meeting weekly with the Medical Doctors For Covid Ethics (MD4CE) group since October 2021. Ana Maria was invited into MD4CE group in the summer of 2022. Ana Maria learned from others in the MD4CE group that I was successfully detoxing people from the Covid-19 vaccines. She approached me early in July and asked me to do a Skype call with her. During the video call she told me that she’s a
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  • DEMOCIDE: U.S. Biolabs In Ukraine Supply Race-Specific Gene Weaponry
    March 26, 2022 by Dr. Ariyana Love
    December 8, 2021
    By Dr. Ariyana Love, N.D.

    Intro:

    In March, I joined Stew Peters Show for a couple of interviews, to provide insight into Putin’s purging of bioweapons labs in Ukraine. Those interviews went viral.

    First interview: Putin’s Secret War: Ukrainian Bioweapon Labs Exposed

    Second interview: Horrifying Russian Report: Ukrainian Biolabs Creating Special Bioweapons For Ethnic Cleansing

    This article is to provide supporting evidence, links and documents for further study.

    GENETIC WARFARE

    Russia’s military operation in Ukraine is entirely justified and in accordance with international law. The US Government, DOD and NATO partners were funding and operating 30 Ukrainian bioweapons labs under a “Covid-19 prevention program” but in actuality, they were producing chimeric pathogens for the “vaccine” Holocaust.

    The but is desperately trying to destroy and hide the evidence that they violated Article 1 of the Biological and Toxic Weapons Convention of 1973. The UN is participating in the cover-up by rebranding the bioweapons facilities as “Public Health laboratories”.

    The same corrupt media trickery and propaganda is being used today by the cabal, to black PR Russia/Putin and create a false narrative that spins confusion and drives division among people. It was no different during Putin’s intervention in Syria.

    Moscow reports that Hunter Biden helped finance a US military ‘bioweapons’ research program in Ukraine. Hunter’s laptop emails provide the supporting evidence that he did in fact help secure millions in funding for US contractor in Ukraine, specializing in deadly pathogen research.

    145 species of bioweapons have been developed in Ukraine in violation of international law and two of them were crossing into Russia. The cabal had used biological weapons in an act of war against not only Russia, but the entire world.

    Routes into Europe were also being mapped. Parasites and insects that carry chimeric pathogens to infect Humans with, were being smuggled out of Ukraine and the bio-samples were being transferred abroad.

    Classified documents captured by Russia reveal a paper trail between Ukrainian biolabs and the Doherty Institute in Australia. Victorian Infectious Diseases Laboratory in Melbourne was caught importing blood serum from Ukrainian biolabs. There’s 350 cryocontainers with samples of blood at the Australian Institute that are being used under the pretense of “antibody research”.

    that Australian mercenaries have been spotted in Ukraine, in the city of Zhitomir, 150km West of Kiev.

    Russia also revealed that the U.S. biolabs in Ukraine created genetic bioweapons to target certain ethnic groups for race-specific ethnic cleansing. A scientific study published in December of 2021, shows that Europeans are the most targeted ethnic group while Ashkenazi Jews (Khazars) are entirely immune to any genetic modification. Now this is some damning evidence.


    Now the DNA harvesting PCR Kits under the guise of “covid testing” should make a lot more sense to you. Your DNA is so valuable to them.

    BACKGROUND

    George Soros has been controlling Ukraine since 2012 and stealing the regions natural resources.

    Former President Barack Obama himself authorized the construction of the biolabs in Ukraine for creating dangerous pathogens, in 2005. It was the Obama/Biden deep state regime established a coup d’etat rule in Kiev, together with the Israeli state.

    Jewish oligarch billionaires in Ukraine with dual nationality to Israel, such as Igor Kolomoisky, funded the neo-Nazi Azov Battalion while the Israeli state armed them.

    Former US Marine Corp Intelligence Officer Scott Ritter told George Galloway “The first troops to be trained by US and British soldiers were the neo-Nazi Azov Battalion”.

    The Azov Nazi’s officially integrated into the National Guard of Ukraine in 2014. Azov violently overthrew the legitimate president of Ukraine and forced their way into the government. The newer Zelensky’s puppet regime has been using internationally banned cluster bombs and other bombs , according to a Human Rights Watch reports, while the militarized Azov Nazi’s have been committing war crimes atrocities against Russian-Christian Ukrainians, especially in Eastern Ukraine. Investigative Journalist Laura Logan confirms there are mass graves in Ukraine from Zelensky’s regime.

    In October 2019, Congress wrote U.S. Secretary Mike Pompeo, asking why the State Department failed to include the Azov Battalion on the Foreign Terrorist Organization list.

    Israeli news Haaretz reported that the Jewish oligarchs will now flee to Israel where they will be given indemnity from their crimes against humanity.

    H5N1 & H1N1

    The US Department of State was able to control everything that happened within the Ukrainian biolabs. Tucker Carlson reported that the U.S. Government released a document in 2020 admitting that the bioweapons facilities in Ukraine are for “vaccine development”.

    The Russian military discovered the plague, anthrax, tularemia, cholera, Ebola, Filoviruses’ and more, were being developed in Ukraine. Ebola is used in the J&J and Sinovax gene editing weaponry while the Filovirus is used in Moderna. Biotech companies are clearly getting their Gain-of-Function pathogens from Ukraine.

    Russia also mentioned that the H5N1 and H1N1 are being produced in the U.S. biolabs. H1N1 induces Smallpox.

    Israeli Mossad Microbiologist Joseph Moshe tried to warn the public in 2009 that a H5N1 biological weapons attack on humanity through “vaccination,” was imminent. He said the H5N1 is even more lethal then the H1N1.

    I found an mRNA vaccine patent for cattle using the H5N1 and H1N1 and the deadly Brucella bacteria. This means the cabal has also been producing weaponry in Ukraine, to poison our food supply. The patent is owned by Khazakstanians.

    Incidentally, there’s a U.S. bioweapons lab in Khazakstan that weaponized Coronavirus for aerosolized dissemination on civilian populations.

    I also found an mRNA vaxxine patent for animals that uses the Brucella melitensis for US and UK cattle.

    WEAPONS TESTING

    Journalist Dilyana Gaytandzheiva reports that the Pentagon has conducted biological experiments on 4,400 soldiers in Ukraine and 1,000 soldiers in Georgia, and unleashed deadly, antibiotic-resistant bacteria on the local civilian population as well as on allied troops, according to leaked documents.

    The documents read that all deaths should be reported to the U.S. Government. The U.S. personnel in these biolabs were given Diplomatic Immunity, although they are not diplomats and they are indemnified from deaths and injuries to the local population.

    The Pentagon project in Ukraine and Georgia was code-named GG-21 for “Arthropod-borne and zoonotic infections”. Arthropod-borne means ticks and other insects carrying deadly pathogens to infect Humans. Zoonotic infections are caused by harmful germs, bacteria, parasites, fungi and mold.

    Blood samples were being obtained from 1,000 military recruits during their physical exams at a military hospital in Gori, Georgia.

    The 13 deadly pathogens that were being tested on the troops are:

    Bacillus anthracis

    Brucella

    Coxiella burnetii

    Francisella tularensis

    Hantavirus

    Rickettsia species

    Bartonella species

    Borrelia species

    Ehlrichia species

    Leptospira species

    Salmonella typhi

    West Nile Virus (WNV)

    The Bacillus anthracis (anthrax) bacteria can be disseminated by aerial spraying. I found a patent with a method for removing plasma (DNA) from Bacillus anthracis bacteria using CRISPR/Cas9 system and it’s owned by China. This is how they get Mycoplasmas.

    Brucella is another deadly bactera. In the 1950s, the US military developed artillery shells and bombs armed with a bacterium that causes a debilitating flu-like disease in humans. In 2001, the US and DARPA artificially sequenced the Brucella suis genome and began applying it to vaccines. Being infected with Brucellosis is like having the flu times ten, though it’s not life-threatening unless you have some other condition. The US Army likes the Brucella suis pathogen because they’re able to debilitate people without killing them, just like “COVID-19”.

    Crimean-Congo hemorrhagic fever (CCHF) has been weaponized using ticks to infect Humans. It has a 40% lethality. Coxiella burnetii and Francisella tularensis are also highly infectious. You need only 10 bacteria to make you sick. The U.S. military was supposed to have destroyed the Francisella tularensis in 1973 because it has up to a 60% lethality.

    TBE is tick-borne and causes encephalitis. Bartonella species cause Lyme Disease. Borrelia bacteria hides inside parasitic worms, causing chronic brain diseases. Ehlrichia is a disease from dogs. WNV (West Nile Virus) is carried by mosquitos.

    CONCLUSION

    Putin just cut off the head of the snake in Ukraine and exposed the whole shit-show. Now let’s make the most of it.

    DEMOCIDE: U.S. Biolabs In Ukraine Supply Race-Specific Gene Weaponry

    https://ambassadorlove.blog/2022/03/26/us-biolabss-in-ukraine-supply-the-vaccine-democide/
    DEMOCIDE: U.S. Biolabs In Ukraine Supply Race-Specific Gene Weaponry March 26, 2022 by Dr. Ariyana Love December 8, 2021 By Dr. Ariyana Love, N.D. Intro: In March, I joined Stew Peters Show for a couple of interviews, to provide insight into Putin’s purging of bioweapons labs in Ukraine. Those interviews went viral. First interview: Putin’s Secret War: Ukrainian Bioweapon Labs Exposed Second interview: Horrifying Russian Report: Ukrainian Biolabs Creating Special Bioweapons For Ethnic Cleansing This article is to provide supporting evidence, links and documents for further study. GENETIC WARFARE Russia’s military operation in Ukraine is entirely justified and in accordance with international law. The US Government, DOD and NATO partners were funding and operating 30 Ukrainian bioweapons labs under a “Covid-19 prevention program” but in actuality, they were producing chimeric pathogens for the “vaccine” Holocaust. The but is desperately trying to destroy and hide the evidence that they violated Article 1 of the Biological and Toxic Weapons Convention of 1973. The UN is participating in the cover-up by rebranding the bioweapons facilities as “Public Health laboratories”. The same corrupt media trickery and propaganda is being used today by the cabal, to black PR Russia/Putin and create a false narrative that spins confusion and drives division among people. It was no different during Putin’s intervention in Syria. Moscow reports that Hunter Biden helped finance a US military ‘bioweapons’ research program in Ukraine. Hunter’s laptop emails provide the supporting evidence that he did in fact help secure millions in funding for US contractor in Ukraine, specializing in deadly pathogen research. 145 species of bioweapons have been developed in Ukraine in violation of international law and two of them were crossing into Russia. The cabal had used biological weapons in an act of war against not only Russia, but the entire world. Routes into Europe were also being mapped. Parasites and insects that carry chimeric pathogens to infect Humans with, were being smuggled out of Ukraine and the bio-samples were being transferred abroad. Classified documents captured by Russia reveal a paper trail between Ukrainian biolabs and the Doherty Institute in Australia. Victorian Infectious Diseases Laboratory in Melbourne was caught importing blood serum from Ukrainian biolabs. There’s 350 cryocontainers with samples of blood at the Australian Institute that are being used under the pretense of “antibody research”. that Australian mercenaries have been spotted in Ukraine, in the city of Zhitomir, 150km West of Kiev. Russia also revealed that the U.S. biolabs in Ukraine created genetic bioweapons to target certain ethnic groups for race-specific ethnic cleansing. A scientific study published in December of 2021, shows that Europeans are the most targeted ethnic group while Ashkenazi Jews (Khazars) are entirely immune to any genetic modification. Now this is some damning evidence. Now the DNA harvesting PCR Kits under the guise of “covid testing” should make a lot more sense to you. Your DNA is so valuable to them. BACKGROUND George Soros has been controlling Ukraine since 2012 and stealing the regions natural resources. Former President Barack Obama himself authorized the construction of the biolabs in Ukraine for creating dangerous pathogens, in 2005. It was the Obama/Biden deep state regime established a coup d’etat rule in Kiev, together with the Israeli state. Jewish oligarch billionaires in Ukraine with dual nationality to Israel, such as Igor Kolomoisky, funded the neo-Nazi Azov Battalion while the Israeli state armed them. Former US Marine Corp Intelligence Officer Scott Ritter told George Galloway “The first troops to be trained by US and British soldiers were the neo-Nazi Azov Battalion”. The Azov Nazi’s officially integrated into the National Guard of Ukraine in 2014. Azov violently overthrew the legitimate president of Ukraine and forced their way into the government. The newer Zelensky’s puppet regime has been using internationally banned cluster bombs and other bombs , according to a Human Rights Watch reports, while the militarized Azov Nazi’s have been committing war crimes atrocities against Russian-Christian Ukrainians, especially in Eastern Ukraine. Investigative Journalist Laura Logan confirms there are mass graves in Ukraine from Zelensky’s regime. In October 2019, Congress wrote U.S. Secretary Mike Pompeo, asking why the State Department failed to include the Azov Battalion on the Foreign Terrorist Organization list. Israeli news Haaretz reported that the Jewish oligarchs will now flee to Israel where they will be given indemnity from their crimes against humanity. H5N1 & H1N1 The US Department of State was able to control everything that happened within the Ukrainian biolabs. Tucker Carlson reported that the U.S. Government released a document in 2020 admitting that the bioweapons facilities in Ukraine are for “vaccine development”. The Russian military discovered the plague, anthrax, tularemia, cholera, Ebola, Filoviruses’ and more, were being developed in Ukraine. Ebola is used in the J&J and Sinovax gene editing weaponry while the Filovirus is used in Moderna. Biotech companies are clearly getting their Gain-of-Function pathogens from Ukraine. Russia also mentioned that the H5N1 and H1N1 are being produced in the U.S. biolabs. H1N1 induces Smallpox. Israeli Mossad Microbiologist Joseph Moshe tried to warn the public in 2009 that a H5N1 biological weapons attack on humanity through “vaccination,” was imminent. He said the H5N1 is even more lethal then the H1N1. I found an mRNA vaccine patent for cattle using the H5N1 and H1N1 and the deadly Brucella bacteria. This means the cabal has also been producing weaponry in Ukraine, to poison our food supply. The patent is owned by Khazakstanians. Incidentally, there’s a U.S. bioweapons lab in Khazakstan that weaponized Coronavirus for aerosolized dissemination on civilian populations. I also found an mRNA vaxxine patent for animals that uses the Brucella melitensis for US and UK cattle. WEAPONS TESTING Journalist Dilyana Gaytandzheiva reports that the Pentagon has conducted biological experiments on 4,400 soldiers in Ukraine and 1,000 soldiers in Georgia, and unleashed deadly, antibiotic-resistant bacteria on the local civilian population as well as on allied troops, according to leaked documents. The documents read that all deaths should be reported to the U.S. Government. The U.S. personnel in these biolabs were given Diplomatic Immunity, although they are not diplomats and they are indemnified from deaths and injuries to the local population. The Pentagon project in Ukraine and Georgia was code-named GG-21 for “Arthropod-borne and zoonotic infections”. Arthropod-borne means ticks and other insects carrying deadly pathogens to infect Humans. Zoonotic infections are caused by harmful germs, bacteria, parasites, fungi and mold. Blood samples were being obtained from 1,000 military recruits during their physical exams at a military hospital in Gori, Georgia. The 13 deadly pathogens that were being tested on the troops are: Bacillus anthracis Brucella Coxiella burnetii Francisella tularensis Hantavirus Rickettsia species Bartonella species Borrelia species Ehlrichia species Leptospira species Salmonella typhi West Nile Virus (WNV) The Bacillus anthracis (anthrax) bacteria can be disseminated by aerial spraying. I found a patent with a method for removing plasma (DNA) from Bacillus anthracis bacteria using CRISPR/Cas9 system and it’s owned by China. This is how they get Mycoplasmas. Brucella is another deadly bactera. In the 1950s, the US military developed artillery shells and bombs armed with a bacterium that causes a debilitating flu-like disease in humans. In 2001, the US and DARPA artificially sequenced the Brucella suis genome and began applying it to vaccines. Being infected with Brucellosis is like having the flu times ten, though it’s not life-threatening unless you have some other condition. The US Army likes the Brucella suis pathogen because they’re able to debilitate people without killing them, just like “COVID-19”. Crimean-Congo hemorrhagic fever (CCHF) has been weaponized using ticks to infect Humans. It has a 40% lethality. Coxiella burnetii and Francisella tularensis are also highly infectious. You need only 10 bacteria to make you sick. The U.S. military was supposed to have destroyed the Francisella tularensis in 1973 because it has up to a 60% lethality. TBE is tick-borne and causes encephalitis. Bartonella species cause Lyme Disease. Borrelia bacteria hides inside parasitic worms, causing chronic brain diseases. Ehlrichia is a disease from dogs. WNV (West Nile Virus) is carried by mosquitos. CONCLUSION Putin just cut off the head of the snake in Ukraine and exposed the whole shit-show. Now let’s make the most of it. DEMOCIDE: U.S. Biolabs In Ukraine Supply Race-Specific Gene Weaponry https://ambassadorlove.blog/2022/03/26/us-biolabss-in-ukraine-supply-the-vaccine-democide/
    AMBASSADORLOVE.BLOG
    DEMOCIDE: U.S. Biolabs In Ukraine Supply Race-Specific Gene Weaponry
    By Dr. Ariyana Love, N.D. Intro: In March, I joined Stew Peters Show for a couple of interviews, to provide insight into Putin’s purging of bioweapons labs in Ukraine. Those interviews went v…
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  • Comedian Jon Stewart exposes COVID-19 SCAMDEMIC in hilarious guest appearance on “The Late Show with Stephen Colbert”

    American comedian, liberal political commentator and "The Daily Show" host Jon Stewart had a hilarious guest appearance on "The Late Show with Stephen Colbert," where he talked about how the Wuhan coronavirus (COVID-19) pandemic was caused and created by science and that it has scammed the public into believing that the virus came from bats.
    Stewart noted that he has a great debt of gratitude to science. He said science has in many ways helped ease the suffering of the pandemic, which was also more than likely caused by science.

    "What are you saying? So, there is a chance that this [virus] was created in a lab?" Colbert bantered.

    This was immediately responded to by Stewart with, "A chance?"

    He then hysterically recited a dialogue with an imaginary person saying, "Oh my God, there is a novel respiratory coronavirus overtaking Wuhan, China. What do we do?" He comedically answered himself with: "Oh no, we can ask the Wuhan novel respiratory coronavirus lab." He argued that the disease is the same name as the laboratory. "That’s just a little too weird, don't you think?"

    He continued by saying he "asked" a scientist how the virus spread to people. Stewart funnily answered himself again, "Well, a pangolin kissed a turtle?" He was on a roll as he continued saying "Maybe a bat flew in the cloaca of the turkey and then it sneezed into my chili and now we all have coronavirus."

    Colbert chimed in, volunteering a piece of information from the official narrative as to how COVID-19 originated: "It could be possible that they have a coronavirus laboratory in Wuhan to study the virus because, in Wuhan, there are a lot of novel coronavirus diseases because of the bat population there."

    Human knowledge is under attack! Governments and powerful corporations are using censorship to wipe out humanity's knowledge base about nutrition, herbs, self-reliance, natural immunity, food production, preparedness and much more. We are preserving human knowledge using AI technology while building the infrastructure of human freedom. Speak freely without censorship at the new decentralized, blockchain-power Brighteon.io. Explore our free, downloadable generative AI tools at Brighteon.AI. Support our efforts to build the infrastructure of human freedom by shopping at HealthRangerStore.com, featuring lab-tested, certified organic, non-GMO foods and nutritional solutions.

    This "enraged" Stewart as he answered sarcastically: "Sure. It's the only place you find bats. You won't find bats anywhere else. Oh wait, Austin, Texas has thousands of them that fly in the caves every night."

    Stewart slams Dems for excusing Biden's obvious cognitive decline during the debate

    Meanwhile, in a recent commentary on his show, Stewart blasted Democrats and the White House for creating excuses for what he described as a "shocking display of cognitive difficulty" by President Joe Biden during the presidential debate late last month.

    "The point is, for a campaign based on honesty and decency, the spin about the debate appears to be blatant b-------, and the redemption tour hasn't gone that much better," Stewart said.

    Stewart played a compilation of Biden clips in which the president read "pause" and "repeat the line" from a teleprompter, along with other lapses in memory, including the time he claimed to have spoken to a long-dead former president of France. According to the Comedy Central host, Biden's poor performance was "recognizable to, unfortunately, anybody who's dealt with aging parents, and it's a hard watch."

    He then said that former President Donald Trump "delivered at the debate to expectation. We expect him to be f------ crazy. But Biden's performance and inability to articulate at times was stunning, like, I could not believe what I was watching."

    "But then it got worse," Stewart went on. "Rather than respecting the American people and having an honest, at least partial, conversation about what we had all seen, we were told immediately, 'These are not the droids you're looking for.'"

    He then streamed another compilation of Democrats making excuses for Biden's poor performance, blaming jet lag and a cold. Stewart noted that the president had been home from Europe for almost two weeks.

    Biden has been facing calls to step down after the catastrophic debate. His allies have argued that Biden is already the nominee and voters have no choice but to back him given the threat of authoritarianism under Trump. But Stewart isn't buying it.

    "'Get On Board Or Shut The F--- Up' is not a particularly compelling pro-democracy bumper sticker," he said.

    Stewart disagrees with some of Biden's supporters' argument that it's too late to change candidates since there are only four months until the election.

    "Four months is for-f-----g-ever," he said and put that timeframe into perspective, citing Britain which just held an election, and France, which had two in one month and even defeated fascism and "still had time to have an affair with Denmark." (Related: Prominent Democratic strategist says it's too late to talk about replacing Biden as party goes into full panic mode over disastrous debate performance.)

    He said he's not calling Biden to drop out but wants the nation to "stress test" the situation to see what options emerge.

    "Do you have any idea how thirsty Americans are for any hint of inspiration or leadership and a release from this choice of a megalomaniac and a suffocating gerontocracy," he said. "It is crushing our f------ spirits."

    The COVID-19 Wuhan laboratory received millions from ex-White House Chief Medical Advisor Anthony Fauci. Watch this video.

    This video is from the InfoWarSSideBand channel on Brighteon.com.

    More related stories:

    WHISTLEBLOWER: CIA bribed its own agents to change their position regarding COVID-19 origins.

    Fauci admits social distancing has no basis; Wuhan lab-leak hypothesis is not conspiracy theory.

    Three scientists from Wuhan lab identified as first carriers of COVID-19.




    http://www.naturalnews.com/2024-07-11-jon-stewart-exposes-covid-scamdemic-hilarious-guesting.html
    Comedian Jon Stewart exposes COVID-19 SCAMDEMIC in hilarious guest appearance on “The Late Show with Stephen Colbert” American comedian, liberal political commentator and "The Daily Show" host Jon Stewart had a hilarious guest appearance on "The Late Show with Stephen Colbert," where he talked about how the Wuhan coronavirus (COVID-19) pandemic was caused and created by science and that it has scammed the public into believing that the virus came from bats. Stewart noted that he has a great debt of gratitude to science. He said science has in many ways helped ease the suffering of the pandemic, which was also more than likely caused by science. "What are you saying? So, there is a chance that this [virus] was created in a lab?" Colbert bantered. This was immediately responded to by Stewart with, "A chance?" He then hysterically recited a dialogue with an imaginary person saying, "Oh my God, there is a novel respiratory coronavirus overtaking Wuhan, China. What do we do?" He comedically answered himself with: "Oh no, we can ask the Wuhan novel respiratory coronavirus lab." He argued that the disease is the same name as the laboratory. "That’s just a little too weird, don't you think?" He continued by saying he "asked" a scientist how the virus spread to people. Stewart funnily answered himself again, "Well, a pangolin kissed a turtle?" He was on a roll as he continued saying "Maybe a bat flew in the cloaca of the turkey and then it sneezed into my chili and now we all have coronavirus." Colbert chimed in, volunteering a piece of information from the official narrative as to how COVID-19 originated: "It could be possible that they have a coronavirus laboratory in Wuhan to study the virus because, in Wuhan, there are a lot of novel coronavirus diseases because of the bat population there." Human knowledge is under attack! Governments and powerful corporations are using censorship to wipe out humanity's knowledge base about nutrition, herbs, self-reliance, natural immunity, food production, preparedness and much more. We are preserving human knowledge using AI technology while building the infrastructure of human freedom. Speak freely without censorship at the new decentralized, blockchain-power Brighteon.io. Explore our free, downloadable generative AI tools at Brighteon.AI. Support our efforts to build the infrastructure of human freedom by shopping at HealthRangerStore.com, featuring lab-tested, certified organic, non-GMO foods and nutritional solutions. This "enraged" Stewart as he answered sarcastically: "Sure. It's the only place you find bats. You won't find bats anywhere else. Oh wait, Austin, Texas has thousands of them that fly in the caves every night." Stewart slams Dems for excusing Biden's obvious cognitive decline during the debate Meanwhile, in a recent commentary on his show, Stewart blasted Democrats and the White House for creating excuses for what he described as a "shocking display of cognitive difficulty" by President Joe Biden during the presidential debate late last month. "The point is, for a campaign based on honesty and decency, the spin about the debate appears to be blatant b-------, and the redemption tour hasn't gone that much better," Stewart said. Stewart played a compilation of Biden clips in which the president read "pause" and "repeat the line" from a teleprompter, along with other lapses in memory, including the time he claimed to have spoken to a long-dead former president of France. According to the Comedy Central host, Biden's poor performance was "recognizable to, unfortunately, anybody who's dealt with aging parents, and it's a hard watch." He then said that former President Donald Trump "delivered at the debate to expectation. We expect him to be f------ crazy. But Biden's performance and inability to articulate at times was stunning, like, I could not believe what I was watching." "But then it got worse," Stewart went on. "Rather than respecting the American people and having an honest, at least partial, conversation about what we had all seen, we were told immediately, 'These are not the droids you're looking for.'" He then streamed another compilation of Democrats making excuses for Biden's poor performance, blaming jet lag and a cold. Stewart noted that the president had been home from Europe for almost two weeks. Biden has been facing calls to step down after the catastrophic debate. His allies have argued that Biden is already the nominee and voters have no choice but to back him given the threat of authoritarianism under Trump. But Stewart isn't buying it. "'Get On Board Or Shut The F--- Up' is not a particularly compelling pro-democracy bumper sticker," he said. Stewart disagrees with some of Biden's supporters' argument that it's too late to change candidates since there are only four months until the election. "Four months is for-f-----g-ever," he said and put that timeframe into perspective, citing Britain which just held an election, and France, which had two in one month and even defeated fascism and "still had time to have an affair with Denmark." (Related: Prominent Democratic strategist says it's too late to talk about replacing Biden as party goes into full panic mode over disastrous debate performance.) He said he's not calling Biden to drop out but wants the nation to "stress test" the situation to see what options emerge. "Do you have any idea how thirsty Americans are for any hint of inspiration or leadership and a release from this choice of a megalomaniac and a suffocating gerontocracy," he said. "It is crushing our f------ spirits." The COVID-19 Wuhan laboratory received millions from ex-White House Chief Medical Advisor Anthony Fauci. Watch this video. This video is from the InfoWarSSideBand channel on Brighteon.com. More related stories: WHISTLEBLOWER: CIA bribed its own agents to change their position regarding COVID-19 origins. Fauci admits social distancing has no basis; Wuhan lab-leak hypothesis is not conspiracy theory. Three scientists from Wuhan lab identified as first carriers of COVID-19. http://www.naturalnews.com/2024-07-11-jon-stewart-exposes-covid-scamdemic-hilarious-guesting.html
    WWW.NATURALNEWS.COM
    Comedian Jon Stewart exposes COVID-19 SCAMDEMIC in hilarious guest appearance on “The Late Show with Stephen Colbert” – NaturalNews.com
    American comedian, liberal political commentator and “The Daily Show” host Jon Stewart had a hilarious guest appearance on “The Late Show with Stephen Colbert,” where he talked about how the Wuhan coronavirus (COVID-19) pandemic was caused and created by science and that it has scammed the public into believing that the virus came from bats. Stewart […]
    Haha
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    0 Comments 1 Shares 2742 Views
  • OLD WORLD ORDER (THE STEW PETERS NETWORK)
    https://www.bitchute.com/video/eo0zHej4lKZn/
    OLD WORLD ORDER (THE STEW PETERS NETWORK) https://www.bitchute.com/video/eo0zHej4lKZn/
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  • Peter Moore from the London Symphony Orchestra presented a masterclass featuring Nathanael Peters, Jihong Son, and Shane Stewart at The U.S. Army Band 2024 American Trombone Workshop. #Masterclass #LondonSymphony #LSO #Trombone #ATW2024 #ATW #Music
    Peter Moore from the London Symphony Orchestra presented a masterclass featuring Nathanael Peters, Jihong Son, and Shane Stewart at The U.S. Army Band 2024 American Trombone Workshop. #Masterclass #LondonSymphony #LSO #Trombone #ATW2024 #ATW #Music
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  • Division III of the National Bass Trombone Solo Competition Finals featured Shane Stewart, Jeremy Mojado, and Kenny Ross playing 2 Songs for Tuba or Bass Trombone by Robert Spillman. #SanFrancisco #SFCM #RiceOwls #GoOwls #UNTProud #UNT #BassTrombone #Trombone #ATW2024 #ATW #Music
    Division III of the National Bass Trombone Solo Competition Finals featured Shane Stewart, Jeremy Mojado, and Kenny Ross playing 2 Songs for Tuba or Bass Trombone by Robert Spillman. #SanFrancisco #SFCM #RiceOwls #GoOwls #UNTProud #UNT #BassTrombone #Trombone #ATW2024 #ATW #Music
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  • Malone has smeared & slandered the leader of the COVID anti-lockdown & anti-COVID mRNA vaccine Dr. Peter McCullough @P_McCulloughMD & we ask why? When I was part of the Freedom Movement, we had weekly meet

    Malone has smeared & slandered the leader of the COVID anti-lockdown & anti-COVID mRNA vaccine Dr. Peter McCullough & we ask why? When I was part of the Freedom Movement, we had weekly meet
    -ings & yes, you saw me on stage with mRNA Malone, BEFORE I understood his greed & con & lies & he was beside himself how come he was not the leader of the anti-COVID & why it was McCullough?

    Dr. Paul Alexander
    Thats the little one sitting behind me on the Lincoln Memorial speech (btw, that day when we were in the holding tent, I overheard Malone telling someone he will be President of the United States one day, needless to say, I grew to understand the psycopathy that day that someone linked to the very mRNA technology that is in the mRNA vaccine that kills us, in that his work has Trump trapped now for he has to come out and say the vaccine is harmful, thinks that the voting public is that stupid):


    This Malone just does not get it, we understand the con, and there is a reason I will leave to McCullough to tell you, his supporters in his time, why McCullough will NEVER ever step foot on a stage where Malone is. Malone knows the distasteful wickedness he pulled.

    I mean, why would he Malone attack Dr. Mike Yeadon?



    Dr. Malone’s limited tolerance for criticism, along with his emphatic responses, has led to an increasing number of individuals and organizations subjected to his public denunciation.

    The list below, derived from Dr. Malone’s past X and Substack posts, details these entities:

    • Dr. Peter Breggin and Ginger Breggin

    • Dr. Mike Yeadon

    • Sasha Latypova

    • Karen Kingston

    • Matthew Crawford

    • Dr. Ben Marble

    • Dr. Judy Mikovitz

    • George Webb

    • Sage Hana on Substack

    • America Out Loud

    • Dr. Jane Ruby

    • Red Voice Media

    • Stew Peters

    • Catherine Austin Fitts (The Solari Report)

    • J. J. Couey

    • Mary Holland (President of Children’s Health Defense)

    • The Wellness Company and its founder Foster Coulson

    • Dr. Kaitlin Kariko

    • Dr. Paul Alexander

    The Washington Post

    • Alex Berenson

    • Dr. Peter McCullough

    • And more. “The list goes on and on,” Dr. Malone has stated.

    https://palexander.substack.com/p/malone-has-smeared-and-slandered

    Join 👇🏻
    https://t.me/DrPaulAlexander
    Malone has smeared & slandered the leader of the COVID anti-lockdown & anti-COVID mRNA vaccine Dr. Peter McCullough @P_McCulloughMD & we ask why? When I was part of the Freedom Movement, we had weekly meet Malone has smeared & slandered the leader of the COVID anti-lockdown & anti-COVID mRNA vaccine Dr. Peter McCullough & we ask why? When I was part of the Freedom Movement, we had weekly meet -ings & yes, you saw me on stage with mRNA Malone, BEFORE I understood his greed & con & lies & he was beside himself how come he was not the leader of the anti-COVID & why it was McCullough? Dr. Paul Alexander Thats the little one sitting behind me on the Lincoln Memorial speech (btw, that day when we were in the holding tent, I overheard Malone telling someone he will be President of the United States one day, needless to say, I grew to understand the psycopathy that day that someone linked to the very mRNA technology that is in the mRNA vaccine that kills us, in that his work has Trump trapped now for he has to come out and say the vaccine is harmful, thinks that the voting public is that stupid): This Malone just does not get it, we understand the con, and there is a reason I will leave to McCullough to tell you, his supporters in his time, why McCullough will NEVER ever step foot on a stage where Malone is. Malone knows the distasteful wickedness he pulled. I mean, why would he Malone attack Dr. Mike Yeadon? Dr. Malone’s limited tolerance for criticism, along with his emphatic responses, has led to an increasing number of individuals and organizations subjected to his public denunciation. The list below, derived from Dr. Malone’s past X and Substack posts, details these entities: • Dr. Peter Breggin and Ginger Breggin • Dr. Mike Yeadon • Sasha Latypova • Karen Kingston • Matthew Crawford • Dr. Ben Marble • Dr. Judy Mikovitz • George Webb • Sage Hana on Substack • America Out Loud • Dr. Jane Ruby • Red Voice Media • Stew Peters • Catherine Austin Fitts (The Solari Report) • J. J. Couey • Mary Holland (President of Children’s Health Defense) • The Wellness Company and its founder Foster Coulson • Dr. Kaitlin Kariko • Dr. Paul Alexander The Washington Post • Alex Berenson • Dr. Peter McCullough • And more. “The list goes on and on,” Dr. Malone has stated. https://palexander.substack.com/p/malone-has-smeared-and-slandered Join 👇🏻 https://t.me/DrPaulAlexander
    PALEXANDER.SUBSTACK.COM
    Malone has smeared & slandered the leader of the COVID anti-lockdown & anti-COVID mRNA vaccine Dr. Peter McCullough & we ask why? When I was part of the Freedom Movement, we had weekly meet
    -ings & yes, you saw me on stage with mRNA Malone, BEFORE I understood his greed & con & lies & he was beside himself how come he was not the leader of the anti-COVID & why it was McCullough?
    Like
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  • There's also a ton of information from the IEC regarding international Standards surrounding Biodigital convergence.

    Quantum Dots are programmable graphene oxide nanoparticles which serve many functions, including biometric data harvesting (spying).

    The demons want to build their Smart Cities from this material!

    https://ambassadorlove.blog/2021/12/17/quantum-dots-dna-barcoding-nano-razors-the-israeli-state/


    Quantum Dots, DNA Barcoding, Nano-Razors & The Israeli State
    December 17, 2021 by Dr. Ariyana Love
    December 2, 2021
    By Dr. Ariyana Love, ND

    In my latest interview with Stew Peter’s, I brought evidence confirming that Dr. Andreas Noack, the good doctor who risked his life to warn humanity of the extreme dangers of the death jab, is in fact deceased.

    Days after Dr. Noack’s mysterious death, a video was leaked revealing Graphene Hydroxide nano-razors inside the Pfizer death jab, under Dark Field Microscopy. The sample is loaded with Graphene Hydroxide.

    You will see an individual Microsphere releasing it’s payload of nanoscale Graphene Hydroxide which looks exactly like razorblades when zoomed in on the individual shiny specs. See more images here.

    LEAKED FOOTAGE: GRAPHENE HYDROXIDE NANO-RAZORBLADES – DARK FIELD MICROSCOPY

    An English translation of this video can be found in the article entitled, Dr. Ariyana Discusses Nano-Biosensors/Nanorazors and Dr. Noack’s Death After He Located Graphene Hydroxide in the COVID Vaccine.

    MICROSPHERES & MICROBUBBLES

    Microbeads and Microspheres are listed as an active ingredient in the Pfizer death jab patent. Microspheres and Microbubbles are listed in the Moderna death jab patent.

    Microspheres and Microbubbles are micrometer size devices approximately equal in size to a red blood cell, according to the NIH. That’s about the width of a Human hair.


    Microbubbles and Microspheres (bottom right)
    Microspheres and Microbubbles are made from Poly(lactic-co-glycolic) acid (PLGA). PLGA is a copolymer made from Graphene Oxide (GO). Graphene Oxide-PLGA nanofibers are used in a host of Food and Drug Administration (FDA) approved “therapeutic” devices. However, the ingredients of these devices are cytotoxic, meaning they destroy cells.

    Graphene Oxide PLGA Toxicity induces an inflammatory response and deadly cytokine storm reaction, according to animal studies. The FDA should be investigated for this.

    Microspheres are coated with gold nanoparticles. Microspheres are used for scaffolding, which is artificial tissue engineering inside the Human body. PubMed writes, “Scaffolds are materials that have been engineered to cause desirable cellular interactions to contribute to the formation of new functional tissues for medical purposes. Cells are often ‘seeded’ into these structures capable of supporting three-dimensional tissue formation.”

    This technology is being used for DNA-based tissue engineering and “scaffolding” of Humans, without their Informed Consent. See more scaffolding images from a Slovakian study of the death jab, here.

    Microbubbles contain one or more “viral vectors coding CRISPR-Cas-9 system“. It’s a “state-of-the-art” drug and chemical delivery method. They contain lab enhanced chimeric proteins of the messenger RNA/DNA. Microbubbles have a lipid and nickel-coated quartz substrate. They contain a drug and chemical payload in the outer, lipid-coating and another payload on the inside.

    Graphene Oxide Nanotubes enable Microbubbles to self-replicate via electrical pulse. They interlink by electrodes. Microbubbles were designed to break through the blood/brain barrier and deliver their drug and chemical payload into brain cells. Ultrasound is used to help Microbubbles breach the blood/brain barrier. Here’s a video animation of how microbubbles / microspheres work to deliver drugs into the brain.

    This gene delivery technology was funded and developed for the purpose of treating sick people, not healthy people. It was intended to be used as a treatment for cancer, not as a medical intervention for our healthy kids.

    The Microbubble and Microsphere devices carry drug and chemical payloads for controlled release of encapsulated DNA. It’s targeted drug delivery can be unloaded over an extended period of time. This is very important to understand. They can be formulated for “sustained release” and programmed to release it’s payload at a later date, over a period of days, weeks, months or years, as the Moderna patent specifies.


    Moderna patent US10703789B2 delayed drug release
    QUANTOM DOTS & MICROBEADS

    Atomic scale nanometer devices called Quantum Dots and Microbeads, are also components of the death jab weapons system. They are found in the Pfizer and Moderna patents.

    These nanoscale technological devices are 1000 times smaller than a micrometer. Quantum Dots have nothing to do with plastic particles, these are carbon based nanocrystals, 10-50 atoms thick, and made from Graphene.

    Quantom Dots are used for DNA barcoding of Humans using CRISPR-Cas-9 technology. They are super conductors made for bio-imaging and bio-tracking of Humans. They too were developed for “therapeutic” use, to eradicate cancers, not to enslave Humans.

    Quantum Dots are artificial, color based, bioluminescent marker genes. They use three colors taken from the enzymatic proteins of insects (Luciferase), glow worms and jellyfish. The chimeric proteins are being barcoded onto Human genes to make them trackable, programmable and encoded, so Human cells will light up, enabling the NWO oligarchs to monitor your every move.

    I discussed Quantum Dots and more with Stew Peters on December 9th, 2021.

    Dr. Ariyana Love on Stew Peters Show, Dec. 9, 2021
    Microbead patent US20110017493A1, verifies that Microbeads “carbon based” (made from Graphene) and Microbead patent ES2784361T3/en specifies that it’s used to create molecular barcodes in Humans.

    Thermo Ficher sells Microbeads and markets them as Dynabeads and SPIONs. See SPIONS here.

    THE ISRAELI STATE

    This technology was developed at the Hebrew University in occupied Jerusalem. The Quantum Dot patent WO201413562A1 is owned by Yissum, a Hebrew University company owned by the Israeli state and co-owned by Nanosys, a Silicon Valley based company. These two companies are sublicensing the technology, worldwide.

    Yissum business partners include Google, Intel, Johnson & Johnson, Merck, Microsoft, and many more, while Samsung has a partnership with Nanosys.

    Moderna’s patents are owned by Israel. Pfizer patents are owned by Israel. Pfizer CEO is in bed with Israel. Moderna is partnered with Israel in medical maleficence.

    Moderna’s CEO Stephane Bancel, wants every man, women and child injected with Moderna’s poison #DeathJab, including INFANTS!


    Is it clear to you now who it is that has the greatest vested interest in branding and enslaving Humans like cattle? The cloning of insect DNA (Luciferase) into Humans is called cross-species genomics. This is the process of manually adding DNA from insects into Humans by transfection, a process also known as cloning, in order to change the genetic makeup of cells. It works by deleting one or more gene from the Human host and encodes Human cells to express the new genetic trait of an insect. Is that what you want to become?


    BIOCHIP & HYDROGEL

    Dr. Pablo Campra mentioned that nano-biosensors are in the death jabs. They can be found in the DARPA patent US7427497B2/en which lists “T-shaped micro-fluidic Biochips”.


    Hydrogels contain the entire mRNA weapons system. They need us saturated with their cloning technology in order to succeed in genetically modifying Humans to the point of patent eligibility. They will do so by injections, masks, nasal swabs, hand sanitizer, aerial spraying, and any other means necessary to achieve their end goal.

    We are in fact being saturated with Graphene Oxide Hydrogels. They’re being inserted into our food, clothing, hair and make-up products, household cleaners, alcohol, pharmaceutical drugs, sanitary items, water supply, etc.

    Ethylene Oxide in masks and on PCR swabs, is in fact Graphene Oxide, Poly(ethylene oxide) Graphene Nanoribbons. The bad news is that Fauci and the NIH funded mRNA nanotechnology which is skin-penetrating and can be dispensed via aerial spraying, as reported by InfoWars. The good news is this weapons system can also be expelled through the skin, if you know how to properly detox. The key to protecting yourself from this biological attack is to boost your immune system and remain on a continued Protocol.

    PROTOCOL

    There is a special natural supplement that disables the operating system, kills the parasites, and removes Graphene and other metals, effectively expelling them from your body. This supplement increases endogenous glutathione by 800%, repairs damage to your cells and to your DNA, and turns genes on, according to scientific research. This medical breakthrough is being used now by doctors who are able to reverse the coagulation cascade in just minutes. You will find this supplement in my Protocol here.

    https://donshafi911.blogspot.com/2024/02/quantum-dots-dna-barcoding-nano-razors.html
    There's also a ton of information from the IEC regarding international Standards surrounding Biodigital convergence. Quantum Dots are programmable graphene oxide nanoparticles which serve many functions, including biometric data harvesting (spying). The demons want to build their Smart Cities from this material! https://ambassadorlove.blog/2021/12/17/quantum-dots-dna-barcoding-nano-razors-the-israeli-state/ Quantum Dots, DNA Barcoding, Nano-Razors & The Israeli State December 17, 2021 by Dr. Ariyana Love December 2, 2021 By Dr. Ariyana Love, ND In my latest interview with Stew Peter’s, I brought evidence confirming that Dr. Andreas Noack, the good doctor who risked his life to warn humanity of the extreme dangers of the death jab, is in fact deceased. Days after Dr. Noack’s mysterious death, a video was leaked revealing Graphene Hydroxide nano-razors inside the Pfizer death jab, under Dark Field Microscopy. The sample is loaded with Graphene Hydroxide. You will see an individual Microsphere releasing it’s payload of nanoscale Graphene Hydroxide which looks exactly like razorblades when zoomed in on the individual shiny specs. See more images here. LEAKED FOOTAGE: GRAPHENE HYDROXIDE NANO-RAZORBLADES – DARK FIELD MICROSCOPY An English translation of this video can be found in the article entitled, Dr. Ariyana Discusses Nano-Biosensors/Nanorazors and Dr. Noack’s Death After He Located Graphene Hydroxide in the COVID Vaccine. MICROSPHERES & MICROBUBBLES Microbeads and Microspheres are listed as an active ingredient in the Pfizer death jab patent. Microspheres and Microbubbles are listed in the Moderna death jab patent. Microspheres and Microbubbles are micrometer size devices approximately equal in size to a red blood cell, according to the NIH. That’s about the width of a Human hair. Microbubbles and Microspheres (bottom right) Microspheres and Microbubbles are made from Poly(lactic-co-glycolic) acid (PLGA). PLGA is a copolymer made from Graphene Oxide (GO). Graphene Oxide-PLGA nanofibers are used in a host of Food and Drug Administration (FDA) approved “therapeutic” devices. However, the ingredients of these devices are cytotoxic, meaning they destroy cells. Graphene Oxide PLGA Toxicity induces an inflammatory response and deadly cytokine storm reaction, according to animal studies. The FDA should be investigated for this. Microspheres are coated with gold nanoparticles. Microspheres are used for scaffolding, which is artificial tissue engineering inside the Human body. PubMed writes, “Scaffolds are materials that have been engineered to cause desirable cellular interactions to contribute to the formation of new functional tissues for medical purposes. Cells are often ‘seeded’ into these structures capable of supporting three-dimensional tissue formation.” This technology is being used for DNA-based tissue engineering and “scaffolding” of Humans, without their Informed Consent. See more scaffolding images from a Slovakian study of the death jab, here. Microbubbles contain one or more “viral vectors coding CRISPR-Cas-9 system“. It’s a “state-of-the-art” drug and chemical delivery method. They contain lab enhanced chimeric proteins of the messenger RNA/DNA. Microbubbles have a lipid and nickel-coated quartz substrate. They contain a drug and chemical payload in the outer, lipid-coating and another payload on the inside. Graphene Oxide Nanotubes enable Microbubbles to self-replicate via electrical pulse. They interlink by electrodes. Microbubbles were designed to break through the blood/brain barrier and deliver their drug and chemical payload into brain cells. Ultrasound is used to help Microbubbles breach the blood/brain barrier. Here’s a video animation of how microbubbles / microspheres work to deliver drugs into the brain. This gene delivery technology was funded and developed for the purpose of treating sick people, not healthy people. It was intended to be used as a treatment for cancer, not as a medical intervention for our healthy kids. The Microbubble and Microsphere devices carry drug and chemical payloads for controlled release of encapsulated DNA. It’s targeted drug delivery can be unloaded over an extended period of time. This is very important to understand. They can be formulated for “sustained release” and programmed to release it’s payload at a later date, over a period of days, weeks, months or years, as the Moderna patent specifies. Moderna patent US10703789B2 delayed drug release QUANTOM DOTS & MICROBEADS Atomic scale nanometer devices called Quantum Dots and Microbeads, are also components of the death jab weapons system. They are found in the Pfizer and Moderna patents. These nanoscale technological devices are 1000 times smaller than a micrometer. Quantum Dots have nothing to do with plastic particles, these are carbon based nanocrystals, 10-50 atoms thick, and made from Graphene. Quantom Dots are used for DNA barcoding of Humans using CRISPR-Cas-9 technology. They are super conductors made for bio-imaging and bio-tracking of Humans. They too were developed for “therapeutic” use, to eradicate cancers, not to enslave Humans. Quantum Dots are artificial, color based, bioluminescent marker genes. They use three colors taken from the enzymatic proteins of insects (Luciferase), glow worms and jellyfish. The chimeric proteins are being barcoded onto Human genes to make them trackable, programmable and encoded, so Human cells will light up, enabling the NWO oligarchs to monitor your every move. I discussed Quantum Dots and more with Stew Peters on December 9th, 2021. Dr. Ariyana Love on Stew Peters Show, Dec. 9, 2021 Microbead patent US20110017493A1, verifies that Microbeads “carbon based” (made from Graphene) and Microbead patent ES2784361T3/en specifies that it’s used to create molecular barcodes in Humans. Thermo Ficher sells Microbeads and markets them as Dynabeads and SPIONs. See SPIONS here. THE ISRAELI STATE This technology was developed at the Hebrew University in occupied Jerusalem. The Quantum Dot patent WO201413562A1 is owned by Yissum, a Hebrew University company owned by the Israeli state and co-owned by Nanosys, a Silicon Valley based company. These two companies are sublicensing the technology, worldwide. Yissum business partners include Google, Intel, Johnson & Johnson, Merck, Microsoft, and many more, while Samsung has a partnership with Nanosys. Moderna’s patents are owned by Israel. Pfizer patents are owned by Israel. Pfizer CEO is in bed with Israel. Moderna is partnered with Israel in medical maleficence. Moderna’s CEO Stephane Bancel, wants every man, women and child injected with Moderna’s poison #DeathJab, including INFANTS! Is it clear to you now who it is that has the greatest vested interest in branding and enslaving Humans like cattle? The cloning of insect DNA (Luciferase) into Humans is called cross-species genomics. This is the process of manually adding DNA from insects into Humans by transfection, a process also known as cloning, in order to change the genetic makeup of cells. It works by deleting one or more gene from the Human host and encodes Human cells to express the new genetic trait of an insect. Is that what you want to become? BIOCHIP & HYDROGEL Dr. Pablo Campra mentioned that nano-biosensors are in the death jabs. They can be found in the DARPA patent US7427497B2/en which lists “T-shaped micro-fluidic Biochips”. Hydrogels contain the entire mRNA weapons system. They need us saturated with their cloning technology in order to succeed in genetically modifying Humans to the point of patent eligibility. They will do so by injections, masks, nasal swabs, hand sanitizer, aerial spraying, and any other means necessary to achieve their end goal. We are in fact being saturated with Graphene Oxide Hydrogels. They’re being inserted into our food, clothing, hair and make-up products, household cleaners, alcohol, pharmaceutical drugs, sanitary items, water supply, etc. Ethylene Oxide in masks and on PCR swabs, is in fact Graphene Oxide, Poly(ethylene oxide) Graphene Nanoribbons. The bad news is that Fauci and the NIH funded mRNA nanotechnology which is skin-penetrating and can be dispensed via aerial spraying, as reported by InfoWars. The good news is this weapons system can also be expelled through the skin, if you know how to properly detox. The key to protecting yourself from this biological attack is to boost your immune system and remain on a continued Protocol. PROTOCOL There is a special natural supplement that disables the operating system, kills the parasites, and removes Graphene and other metals, effectively expelling them from your body. This supplement increases endogenous glutathione by 800%, repairs damage to your cells and to your DNA, and turns genes on, according to scientific research. This medical breakthrough is being used now by doctors who are able to reverse the coagulation cascade in just minutes. You will find this supplement in my Protocol here. https://donshafi911.blogspot.com/2024/02/quantum-dots-dna-barcoding-nano-razors.html
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  • NATO 'scrambles jets', Kremlin claims, as Putin sends two nuclear-capable missile carriers over Norwegian Sea

    The Kremlin launched two missile carriers to fly over the Norwegian Sea
    NATO scrambled jets in response, Russia has claimed
    Tensions between Russia and the bloc have been steadily rising

    NATO has scrambled warplanes to confront a pair of nuclear-capable missile carriers that were seen patrolling the Norwegian Sea today, Russia has claimed.

    The Kremlin once again taunted the bloc by launching two TU-95MS planes to patrol the Norwegian Sea, which were escorted by a group of Su35S aircraft.
    READ

    https://www.dailymail.co.uk/news/article-13074167/NATO-scrambles-jets-Kremlin-claims-Putin-sends-two-nuclear-capable-missile-carriers-Norwegian-Sea.html


    NATO 'scrambles jets', Kremlin claims, as Putin sends two nuclear-capable missile carriers over Norwegian Sea
    By Will Stewart and Perkin Amalaraj 13:58 GMT 12 Feb 2024 , updated 14:58 GMT 12 Feb 2024

    The Kremlin launched two missile carriers to fly over the Norwegian Sea
    NATO scrambled jets in response, Russia has claimed
    Tensions between Russia and the bloc have been steadily rising
    NATO has scrambled warplanes to confront a pair of nuclear-capable missile carriers that were seen patrolling the Norwegian Sea today, Russia has claimed.

    Advertisement
    Advertisement
    The Kremlin once again taunted the bloc by launching two TU-95MS planes to patrol the Norwegian Sea, which were escorted by a group of Su35S aircraft.

    The five-hour flight also saw 'fighters from foreign countries' accompany the unit, though Moscow did not specify which Wester air forces were deployed. An MoD source told MailOnline that the RAF have not launched any planes in response to the fly-over.

    The Norwegian Sea is bordered to the south by Britain - the north of Shetland, to the east by Norway, and to the west by Iceland.

    'The flight was carried out in strict accordance with international rules for the use of airspace,' said Lieutenant-General Sergei Kobylash, commander of Russian long-range aviation.


    NATO scrambles jets as Russia sends two nuclear missiles over sea

    Russian Tu-95MS nuclear-capable strategic missile carriers flew over the Norwegian Sea
    Russian Tu-95MS nuclear-capable strategic missile carriers flew over the Norwegian Sea
    The flights come amid warnings from Western politicians and military commanders about the threat of Russia triggering a Third World War
    The flights come amid warnings from Western politicians and military commanders about the threat of Russia triggering a Third World War
    'Long-range aviation pilots regularly fly over the neutral waters of the Arctic, North Atlantic, Pacific Ocean, Black and Baltic Seas.'

    READ MORE: Elon Musk is hailed in Russia as 'Colonel Muskov' after it's claimed Putin's forces are using his Starlink system to aid Ukrainian invasion
    The flights come amid warnings from Western politicians and military commanders about the threat of Russia triggering a Third World War in the coming years.

    But the UK's overstretched armed forces may be unable to effectively fight in a potential world war, as chronic shortages of troops and equipment are being covered up in a 'veil of secrecy', MPs have warned.

    In a damning report released last week, the Defence Select Committee concluded the Army is the UK's 'weakest service' due to 'significant capability deficiencies' – which included drastic shortages of vehicles, tanks and even ammunition.

    After facing a wall of silence while compiling their Ready For War report, the MPs urged military top brass and Ministers to be more transparent about the shortcomings so they can be addressed urgently.

    The report further highlights war-readiness issues with the Royal Navy's £3.5billion aircraft carriers, too.

    Ukrainian servicemen light a fire with gun powder to get warm near the city of Bakhmut
    Ukrainian servicemen light a fire with gun powder to get warm near the city of Bakhmut
    Ukrainian serviceman of the Ukrainian Volunteer Army stands at a fortified position, at an undisclosed location next to the Vuhledar frontline
    Ukrainian serviceman of the Ukrainian Volunteer Army stands at a fortified position, at an undisclosed location next to the Vuhledar frontline
    Firefighters try to extinguish the fire broke out on a destroyed building after Russian shelling
    Firefighters try to extinguish the fire broke out on a destroyed building after Russian shelling
    Despite spending about £50billion a year on defence, 'sustained ongoing investment' is needed for the UK to fight a 'high-intensity war', the report concludes.

    READ MORE: Russia mocks the West's fury over Trump after he said he'd encourage Putin to attack NATO nations who fail to pay bills - 'Do they seriously think we will bomb defaulters once a quarter?'
    Witnesses told the inquiry that the Armed Forces would struggle in a major conflict, claiming the British Army does not have enough new infantry fighting vehicles, Challenger tanks or adequate missile defence capabilities.

    Advertisement
    Advertisement
    The Royal Navy is suffering from delays to a new frigate programme and an 'over-tasked' aircraft fleet, while the RAF has a shortfall of combat aircraft, delays to new Chinook helicopters and too few pilots.

    The heads of the Forces also raised concerns about stockpiles used by Ukraine reducing the amount available to the UK.

    The report warned of 'capacity shortfalls', with the MoD admitting to only recruiting five service personnel for every eight who leave.

    Earlier this week, Putin told Tucker Carlson that a Russian defeat in the war he unleashed by invading Ukraine is 'impossible' and 'will never happen'.

    There is also acute concern in eastern Europe over the prospect of a re-elected Donald Trump downscaling NATO.

    Putin told Carlson 'we have no interest in Poland, Latvia or anywhere else- why would we?

    'We simply have no interest..... It is absolutely out of the question.'

    However, he earlier made similar claims about using force to grab Crimea and other areas of Ukraine.

    MailOnline has contacted NATO and the UK's Ministry of Defence for comment.

    https://donshafi911.blogspot.com/2024/02/nato-scrambles-jets-kremlin-claims-as.html
    NATO 'scrambles jets', Kremlin claims, as Putin sends two nuclear-capable missile carriers over Norwegian Sea ➡️The Kremlin launched two missile carriers to fly over the Norwegian Sea ➡️NATO scrambled jets in response, Russia has claimed ➡️Tensions between Russia and the bloc have been steadily rising NATO has scrambled warplanes to confront a pair of nuclear-capable missile carriers that were seen patrolling the Norwegian Sea today, Russia has claimed. The Kremlin once again taunted the bloc by launching two TU-95MS planes to patrol the Norwegian Sea, which were escorted by a group of Su35S aircraft. READ https://www.dailymail.co.uk/news/article-13074167/NATO-scrambles-jets-Kremlin-claims-Putin-sends-two-nuclear-capable-missile-carriers-Norwegian-Sea.html NATO 'scrambles jets', Kremlin claims, as Putin sends two nuclear-capable missile carriers over Norwegian Sea By Will Stewart and Perkin Amalaraj 13:58 GMT 12 Feb 2024 , updated 14:58 GMT 12 Feb 2024 The Kremlin launched two missile carriers to fly over the Norwegian Sea NATO scrambled jets in response, Russia has claimed Tensions between Russia and the bloc have been steadily rising NATO has scrambled warplanes to confront a pair of nuclear-capable missile carriers that were seen patrolling the Norwegian Sea today, Russia has claimed. Advertisement Advertisement The Kremlin once again taunted the bloc by launching two TU-95MS planes to patrol the Norwegian Sea, which were escorted by a group of Su35S aircraft. The five-hour flight also saw 'fighters from foreign countries' accompany the unit, though Moscow did not specify which Wester air forces were deployed. An MoD source told MailOnline that the RAF have not launched any planes in response to the fly-over. The Norwegian Sea is bordered to the south by Britain - the north of Shetland, to the east by Norway, and to the west by Iceland. 'The flight was carried out in strict accordance with international rules for the use of airspace,' said Lieutenant-General Sergei Kobylash, commander of Russian long-range aviation. NATO scrambles jets as Russia sends two nuclear missiles over sea Russian Tu-95MS nuclear-capable strategic missile carriers flew over the Norwegian Sea Russian Tu-95MS nuclear-capable strategic missile carriers flew over the Norwegian Sea The flights come amid warnings from Western politicians and military commanders about the threat of Russia triggering a Third World War The flights come amid warnings from Western politicians and military commanders about the threat of Russia triggering a Third World War 'Long-range aviation pilots regularly fly over the neutral waters of the Arctic, North Atlantic, Pacific Ocean, Black and Baltic Seas.' READ MORE: Elon Musk is hailed in Russia as 'Colonel Muskov' after it's claimed Putin's forces are using his Starlink system to aid Ukrainian invasion The flights come amid warnings from Western politicians and military commanders about the threat of Russia triggering a Third World War in the coming years. But the UK's overstretched armed forces may be unable to effectively fight in a potential world war, as chronic shortages of troops and equipment are being covered up in a 'veil of secrecy', MPs have warned. In a damning report released last week, the Defence Select Committee concluded the Army is the UK's 'weakest service' due to 'significant capability deficiencies' – which included drastic shortages of vehicles, tanks and even ammunition. After facing a wall of silence while compiling their Ready For War report, the MPs urged military top brass and Ministers to be more transparent about the shortcomings so they can be addressed urgently. The report further highlights war-readiness issues with the Royal Navy's £3.5billion aircraft carriers, too. Ukrainian servicemen light a fire with gun powder to get warm near the city of Bakhmut Ukrainian servicemen light a fire with gun powder to get warm near the city of Bakhmut Ukrainian serviceman of the Ukrainian Volunteer Army stands at a fortified position, at an undisclosed location next to the Vuhledar frontline Ukrainian serviceman of the Ukrainian Volunteer Army stands at a fortified position, at an undisclosed location next to the Vuhledar frontline Firefighters try to extinguish the fire broke out on a destroyed building after Russian shelling Firefighters try to extinguish the fire broke out on a destroyed building after Russian shelling Despite spending about £50billion a year on defence, 'sustained ongoing investment' is needed for the UK to fight a 'high-intensity war', the report concludes. READ MORE: Russia mocks the West's fury over Trump after he said he'd encourage Putin to attack NATO nations who fail to pay bills - 'Do they seriously think we will bomb defaulters once a quarter?' Witnesses told the inquiry that the Armed Forces would struggle in a major conflict, claiming the British Army does not have enough new infantry fighting vehicles, Challenger tanks or adequate missile defence capabilities. Advertisement Advertisement The Royal Navy is suffering from delays to a new frigate programme and an 'over-tasked' aircraft fleet, while the RAF has a shortfall of combat aircraft, delays to new Chinook helicopters and too few pilots. The heads of the Forces also raised concerns about stockpiles used by Ukraine reducing the amount available to the UK. The report warned of 'capacity shortfalls', with the MoD admitting to only recruiting five service personnel for every eight who leave. Earlier this week, Putin told Tucker Carlson that a Russian defeat in the war he unleashed by invading Ukraine is 'impossible' and 'will never happen'. There is also acute concern in eastern Europe over the prospect of a re-elected Donald Trump downscaling NATO. Putin told Carlson 'we have no interest in Poland, Latvia or anywhere else- why would we? 'We simply have no interest..... It is absolutely out of the question.' However, he earlier made similar claims about using force to grab Crimea and other areas of Ukraine. MailOnline has contacted NATO and the UK's Ministry of Defence for comment. https://donshafi911.blogspot.com/2024/02/nato-scrambles-jets-kremlin-claims-as.html
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  • So many unanswered questions surrounding Oct. 7th that we’ll never get answers to.

    Kind of important considering the fact that they’re using this to try send the world into a nuclear war no?

    @realstewpeters

    https://x.com/itsmorganariel/status/1756495193912574345?s=46
    So many unanswered questions surrounding Oct. 7th that we’ll never get answers to. Kind of important considering the fact that they’re using this to try send the world into a nuclear war no? @realstewpeters https://x.com/itsmorganariel/status/1756495193912574345?s=46
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