• More Proof mRNA Shots Edit Human Genome
    New Study Again Shows LINE-1 "Junk DNA" Does The Dirty Work

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

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

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

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

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

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

    Share

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

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

    … such high levels are induced by mRNA vaccination.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

    The first theory is the most concerning.

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

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

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

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

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

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

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

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

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

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

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


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

    COVID Vaccine Gene Could Integrate Into Human Cancer Cells: Researcher
    (CROCOTHERY/Shutterstock)
    Following his discovery of DNA contamination in COVID-19 mRNA vaccines, genomic researcher Kevin McKernan has recently found that the DNA in these vaccines can potentially integrate into human DNA.

    The COVID-19 vaccine spike sequence was detected in two types of chromosomes in cancer cell lines following exposure to the COVID-19 mRNA vaccine. Mr. McKernan’s findings, which he presents on his Substack blog, haven’t been peer-reviewed.
    These are expected to be “rare events,” but they can happen, Mr. McKernan told The Epoch Times.
    DNA Integration

    Since the introduction of the COVID-19 mRNA vaccines, some members of the public have been concerned that the vaccines may modify human DNA by combining their sequences with the human genome.

    Story continues below advertisement

    “Fact-checkers” refuted this, saying mRNA cannot be changed into DNA. Yet Mr. McKernan’s earlier work shows that DNA in the vaccine vials may be capable of changing human DNA.
    Ulrike Kämmerer, a professor of human biology at the University Hospital of Würzburg in Germany, conducted earlier stages of this research.

    Exposing breast and ovarian human cancer cells to Pfizer and Moderna mRNA vaccines, Ms. Kämmerer found that about half of the cells expressed the COVID-19 spike protein on their cellular surface, indicating that they had absorbed the vaccines.

    Mr. McKernan then performed gene sequencing and found that these cells and their descendant cells contained vaccine DNA.

    Story continues below advertisement

    After this, he tested to see whether any vaccine DNA combined with the cancer cell DNA, a process known as DNA integration. Integration is more of a concern in healthy cells than cancer cells because it disrupts cells’ genetic stability and integrity, increasing cancer risk.

    However, because cancer cells already have unstable DNA, the effects of DNA integration are less clear.

    Currently, in biomedical research, most experiments are carried out in cancer cell lines, as they are easier to obtain, experiment on, and maintain in the laboratory.

    Mr. McKernan detected vaccine DNA sequences on two chromosomes in the cancer cell lines: chromosome 9 and chromosome 12. The sequencing machine detected both instances of integration twice. It is important to get two readings of the DNA integration to ensure that the integration is not a result of misreading or random error, he said.

    Story continues below advertisement

    “The integration of ‘vaccine’ genetic information into the genome of cells was not such a surprise for me—more the confirmation of what we had to expect, unfortunately,” he told The Epoch Times.

    Mr. McKernan said it is unsurprising that integration was detected on only two chromosomes with two readings of each integration. This is because integration is rare, and the genes must be sequenced many times to get more sensitive results.

    The current findings are still preliminary, he said. More tests are also needed to determine whether DNA integration could be passed on to descendant cancer cells and whether this may affect cancer patients.

    Also, since the test was conducted in cancer cells and not in healthy human cells, it does not suggest the same integration would occur in healthy human cells.

    Story continues below advertisement

    However, Hiroshi Arakawa, a researcher at the Institute of Molecular Oncology who has a doctorate in molecular biology and immunology, wrote in his blog that “what happens in cultured cells can also occur in normal cells” after examining Mr. McKernan’s data.
    His review of Mr. McKernan’s data also found signs of DNA integration at chromosomes 9 and 12.

    “A wide variety of abnormalities can occur [in normal cells] depending on the site of genome integration,” Mr. Arakawa said.
    Not Random Events

    The two integration events into chromosome 9 occurred at the same place, as did the integration events into chromosome 12.

    Mr. McKernan said the odds of this occurring are one in 3 billion, highlighting that where the DNA integrates may not be random.

    Story continues below advertisement

    “There’s likely hotspots for this,” he told The Epoch Times, highlighting that in the human genome, jumping genes—short segments of DNA sequences—tend to “jump” into highly activated areas of DNA.

    Highly activated DNA tends to play important roles in the human body.

    The DNA integration into chromosome 12 occurred within the FAIM2 gene. Once activated, this gene creates a protein involved in programmed cell death. Since cancer cells evade cell death, the integration at chromosome 12 may be a survival-driven change.
    Vaccine DNA Is Active in the Cells

    Mr. McKernan said he believes that vaccine DNA is highly active in cancer cells. His sequencing machine detected the DNA of cancer cells 30 times but detected spike DNA 3,000 times.

    Not only did he detect much higher levels of vaccine DNA, but he also detected new variants in certain segments of the vaccine DNA.

    Story continues below advertisement

    These new DNA variations were not observed in unvaccinated cancer cells nor in the vaccine not exposed to the cancer cells.

    Mr. McKernan said he believes that these new gene variants likely occurred because the cancer cell made copies of the vaccine DNA and created small errors.

    What he and his team have found contradicts the latest arguments from fact-checkers claiming that the DNA from the mRNA vaccines cannot get into the cell, nor can it be active, he said.
    DNA Contamination From mRNA Vaccine Manufacturing

    DNA is present in the COVID-19 mRNA vaccines because of the manufacturing process.
    This has been verified by the U.S. Food and Drug Administration (FDA), Health Canada, and the European Medicines Agency.
    The mRNA vaccines are made from DNA; some of this DNA persists in the final product because of insufficient clearance.
    Initially, Pfizer reported that it would use a PCR machine to produce the DNA for its mRNA vaccine. The PCR machine first makes many copies of DNA, which is then sequenced into RNA.

    However, because this process wouldn’t be fast enough to meet demands, the vaccine manufacturers switched to using bacteria to mass-produce DNA as the template for the mRNA vaccine.

    In this process, vaccine manufacturers introduce bacterial DNA containing the vaccine spike sequences. The bacteria make many copies of this spike DNA as they divide. This spike DNA is then harvested and transcribed into mRNA in a machine. The mRNA is then packaged into lipid nanoparticles for use in vaccination.

    However, some bacterial DNA containing spike protein and other sequences could be packaged into lipid nanoparticles during the process, which would then be transported into cells during vaccination. Mr. McKernan’s earlier works have demonstrated this.
    Works by molecular virologist David Speicher have shown that the amount of DNA in the mRNA vaccine vials is higher than the FDA’s allowable threshold of 10 nanograms per vaccine dose.
    Mr. McKernan highlighted that compared with previous vaccines, mainly composed of naked DNA that had difficulty entering the cells, the DNA carried in the mRNA vaccines presents greater health risks, as it is packed into lipid nanoparticles and delivered straight into the cells.

    https://www.theepochtimes.com/health/covid-vaccine-gene-could-integrate-into-human-cancer-cells-researcher-5604184
    COVID Vaccine Gene Could Integrate Into Human Cancer Cells: Researcher What Mr. McKernan and his team have found contradicts the latest arguments from fact-checkers. COVID Vaccine Gene Could Integrate Into Human Cancer Cells: Researcher (CROCOTHERY/Shutterstock) Following his discovery of DNA contamination in COVID-19 mRNA vaccines, genomic researcher Kevin McKernan has recently found that the DNA in these vaccines can potentially integrate into human DNA. The COVID-19 vaccine spike sequence was detected in two types of chromosomes in cancer cell lines following exposure to the COVID-19 mRNA vaccine. Mr. McKernan’s findings, which he presents on his Substack blog, haven’t been peer-reviewed. These are expected to be “rare events,” but they can happen, Mr. McKernan told The Epoch Times. DNA Integration Since the introduction of the COVID-19 mRNA vaccines, some members of the public have been concerned that the vaccines may modify human DNA by combining their sequences with the human genome. Story continues below advertisement “Fact-checkers” refuted this, saying mRNA cannot be changed into DNA. Yet Mr. McKernan’s earlier work shows that DNA in the vaccine vials may be capable of changing human DNA. Ulrike Kämmerer, a professor of human biology at the University Hospital of Würzburg in Germany, conducted earlier stages of this research. Exposing breast and ovarian human cancer cells to Pfizer and Moderna mRNA vaccines, Ms. Kämmerer found that about half of the cells expressed the COVID-19 spike protein on their cellular surface, indicating that they had absorbed the vaccines. Mr. McKernan then performed gene sequencing and found that these cells and their descendant cells contained vaccine DNA. Story continues below advertisement After this, he tested to see whether any vaccine DNA combined with the cancer cell DNA, a process known as DNA integration. Integration is more of a concern in healthy cells than cancer cells because it disrupts cells’ genetic stability and integrity, increasing cancer risk. However, because cancer cells already have unstable DNA, the effects of DNA integration are less clear. Currently, in biomedical research, most experiments are carried out in cancer cell lines, as they are easier to obtain, experiment on, and maintain in the laboratory. Mr. McKernan detected vaccine DNA sequences on two chromosomes in the cancer cell lines: chromosome 9 and chromosome 12. The sequencing machine detected both instances of integration twice. It is important to get two readings of the DNA integration to ensure that the integration is not a result of misreading or random error, he said. Story continues below advertisement “The integration of ‘vaccine’ genetic information into the genome of cells was not such a surprise for me—more the confirmation of what we had to expect, unfortunately,” he told The Epoch Times. Mr. McKernan said it is unsurprising that integration was detected on only two chromosomes with two readings of each integration. This is because integration is rare, and the genes must be sequenced many times to get more sensitive results. The current findings are still preliminary, he said. More tests are also needed to determine whether DNA integration could be passed on to descendant cancer cells and whether this may affect cancer patients. Also, since the test was conducted in cancer cells and not in healthy human cells, it does not suggest the same integration would occur in healthy human cells. Story continues below advertisement However, Hiroshi Arakawa, a researcher at the Institute of Molecular Oncology who has a doctorate in molecular biology and immunology, wrote in his blog that “what happens in cultured cells can also occur in normal cells” after examining Mr. McKernan’s data. His review of Mr. McKernan’s data also found signs of DNA integration at chromosomes 9 and 12. “A wide variety of abnormalities can occur [in normal cells] depending on the site of genome integration,” Mr. Arakawa said. Not Random Events The two integration events into chromosome 9 occurred at the same place, as did the integration events into chromosome 12. Mr. McKernan said the odds of this occurring are one in 3 billion, highlighting that where the DNA integrates may not be random. Story continues below advertisement “There’s likely hotspots for this,” he told The Epoch Times, highlighting that in the human genome, jumping genes—short segments of DNA sequences—tend to “jump” into highly activated areas of DNA. Highly activated DNA tends to play important roles in the human body. The DNA integration into chromosome 12 occurred within the FAIM2 gene. Once activated, this gene creates a protein involved in programmed cell death. Since cancer cells evade cell death, the integration at chromosome 12 may be a survival-driven change. Vaccine DNA Is Active in the Cells Mr. McKernan said he believes that vaccine DNA is highly active in cancer cells. His sequencing machine detected the DNA of cancer cells 30 times but detected spike DNA 3,000 times. Not only did he detect much higher levels of vaccine DNA, but he also detected new variants in certain segments of the vaccine DNA. Story continues below advertisement These new DNA variations were not observed in unvaccinated cancer cells nor in the vaccine not exposed to the cancer cells. Mr. McKernan said he believes that these new gene variants likely occurred because the cancer cell made copies of the vaccine DNA and created small errors. What he and his team have found contradicts the latest arguments from fact-checkers claiming that the DNA from the mRNA vaccines cannot get into the cell, nor can it be active, he said. DNA Contamination From mRNA Vaccine Manufacturing DNA is present in the COVID-19 mRNA vaccines because of the manufacturing process. This has been verified by the U.S. Food and Drug Administration (FDA), Health Canada, and the European Medicines Agency. The mRNA vaccines are made from DNA; some of this DNA persists in the final product because of insufficient clearance. Initially, Pfizer reported that it would use a PCR machine to produce the DNA for its mRNA vaccine. The PCR machine first makes many copies of DNA, which is then sequenced into RNA. However, because this process wouldn’t be fast enough to meet demands, the vaccine manufacturers switched to using bacteria to mass-produce DNA as the template for the mRNA vaccine. In this process, vaccine manufacturers introduce bacterial DNA containing the vaccine spike sequences. The bacteria make many copies of this spike DNA as they divide. This spike DNA is then harvested and transcribed into mRNA in a machine. The mRNA is then packaged into lipid nanoparticles for use in vaccination. However, some bacterial DNA containing spike protein and other sequences could be packaged into lipid nanoparticles during the process, which would then be transported into cells during vaccination. Mr. McKernan’s earlier works have demonstrated this. Works by molecular virologist David Speicher have shown that the amount of DNA in the mRNA vaccine vials is higher than the FDA’s allowable threshold of 10 nanograms per vaccine dose. Mr. McKernan highlighted that compared with previous vaccines, mainly composed of naked DNA that had difficulty entering the cells, the DNA carried in the mRNA vaccines presents greater health risks, as it is packed into lipid nanoparticles and delivered straight into the cells. https://www.theepochtimes.com/health/covid-vaccine-gene-could-integrate-into-human-cancer-cells-researcher-5604184
    WWW.THEEPOCHTIMES.COM
    COVID Vaccine Gene Could Integrate Into Human Cancer Cells: Researcher
    What Mr. McKernan and his team have found contradicts the latest arguments from fact-checkers.
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  • DNA contamination in Covid vaccines DOES get into human cells, new evidence shows
    It also appears that the contamination enters the cell nucleus and integrates with human DNA

    Rebekah Barnett
    Regulators and fact checkers claim that plasmid DNA contamination in the mRNA Covid vaccines can’t change your genomic DNA, but new evidence suggests that it actually can.

    The fact checkers assert that DNA contamination poses no risk to your genomic DNA because your body will naturally destroy any contaminant DNA before it even gets into the cells.

    Even if the contaminant DNA could get into cells, there’s no way it can enter the cell nucleus, where genomic integration events occur, they say.

    And even if the contaminant DNA could enter the nucleus, which it can’t, it still couldn’t genomically integrate unless specific enzymes are present, they say.

    However, results from independent lab testing conducted on ovarian cancer cell lines show that contaminant DNA from Pfizer’s Covid vaccine not only crossed into the cells, but that it survived multiple cell divisions. This is suggestive that the contaminant DNA is able to transfect (enter) the cell nucleus, and that it integrated with the human cell DNA.

    TLDR

    1. Scientists claim that Pfizer vaccine contaminant DNA has been detected in ovarian cancer cell line DNA, but they do not yet know if it’s chromosomal (heritable) or extra-chromosomal DNA (not heritable)

    2. This is an in vitro (in a lab dish) finding, and needs to be replicated in vivo (in a human patient)

    3. As the finding is specific to cancer cell lines, it is not generalisable, but scientists say it may give an indication of what cancer patients in remission could experience after mRNA Covid vaccination

    4. This finding calls into question fact checker claims that mRNA Covid vaccine DNA contamination can't enter cells, can't enter the nucleus, and cannot integrate with human DNA.
    Last year, Boston-based genomics scientist Kevin McKernan made the shocking discovery that the mRNA Covid vaccines are contaminated with excessive levels of plasmid DNA, an artefact of the vaccine production process.

    McKernan’s findings were soon confirmed by multiple independent labs around the world for both the Pfizer and Moderna mono- and bi-valent vaccines, including lots approved for children, with one Canadian study led by Dr David Speicher concluding that there are “billions to hundreds of billions of DNA molecules per dose.”

    Scientists including McKernan, University of South Carolina cancer genomics scientist Dr Phillip Buckhaults, and Dr Wafik El-Diery, head of the Cancer Centre at Brown University, expressed concerns that fragments of plasmid DNA contamination could cause adverse events, autoimmune problems and cancers in some patients.

    But perhaps most significantly, there is also a theoretical risk of the contaminant DNA integrating with patients’ chromosomal DNA and modifying the human genome. This is of particular concern with the Pfizer vaccine, which contains an SV40 enhancer sequence, used in gene therapies “to drive DNA into the nucleus,” explains McKernan.

    While regulators have taken a ‘wait and see’ approach, independent scientists, including McKernan, have been more proactive, initiating experiments testing for evidence of genomic integration.

    Now, the first results are in.

    In an experiment conducted together with German molecular biologist Dr Ulrike Kämmerer, McKernan has detected vaccine contaminant DNA in ovarian cancer cell lines treated with Pfizer’s Covid vaccine.

    The scientists found a chimeric combination of human ovarian cell line DNA and spike sequence DNA derived from the contaminating plasmid at at least one, and possibly two sites.

    “If anything, this work has put to bed the question regarding if this contaminant DNA gets into the cell, and the chimeric human and contaminant spike DNA sequences imply it has entered the nucleus,” McKernan says.

    “The PCR and sequencing data both demonstrate the vaccine is getting into the cell and surviving cell passaging. It is likely bioactive and being partially replicated.”

    To reach this finding, Dr Kämmerer first treated ovarian cancer cell lines with mRNA Covid vaccines, using cells treated with AstraZeneca and Janssen vaccines as controls.

    The cells were then ‘passaged’, meaning they were left to divide and replicate numerous times. This has the effect of “rinsing away residual vaccine,” explains McKernan.

    Immunohistochemistry (IHC) was then performed, a staining process that Dr Kämmerer used to detect levels of spike protein expression produced by the vaccine modified-RNA.

    This was to confirm that the lipid nanoparticles (LNPs) carrying mod-RNA and plasmid DNA contamination “did their job and delivered the payload,” says McKernan. Measuring how many cells expressed spike protein also allowed the scientists to determine how much of the vaccine to treat the cells with.


    Immunohistochemistry performed with Pfizer top left, AstraZeneca top right as a control. Source: Kevin McKernan’s Substack
    Cell lines were then sent in cold storage to McKernan’s Boston lab, where his team used qPCR to screen which samples to sequence the cell line DNA.

    “What we found is, [contaminant] DNA that is getting transfected into ovarian cancer cell lines is replicating in the cells,” says McKernan, noting that the ratio of vaccine contaminant DNA to human cell DNA was “higher than we expected.”

    Chimeric sequences of human and vaccine contaminant DNA were detected at two sites: chromosomes 9 and 12, with the evidence for the latter being the strongest. “But we don't know if it's extra-chromosomal or whether it's chromosomal because of the Illumina (short read) method we used to sequence,” explains McKernan.


    Source: Kevin McKernan’s Substack
    Extra-chromosomal DNA is not part of the chromosome, and is therefore less likely to replicate and to be heritable. Chromosomal DNA, on the other hand, is heritable and more likely to be replicated. A third category, mitochondrial DNA, is heritable, but only from the maternal line.

    You can read a detailed account of methods and findings via McKernan’s Substack article, ‘Vaccine targeted qPCR of Cancer Cell Lines treated with BNT162b2.’

    ‘Major advance,’ but clinical implications are limited

    McKernan emphasises that these findings cannot be generalised, stating that “it is too early to make comments on the clinical implications.”

    “The study is performed in ovarian cancer cell lines. It is not performed in patient cells, but this is a proxy for what might happen in an ovarian cancer patient who's in remission,” says McKernan, especially as there is evidence that the LNPs go to the ovaries.

    The risk for patients in this scenario is that integration events with contaminant DNA might cause aberrant cell growth, which poses a risk to immune suppression of new cancer cells.

    McKernan notes that his experiment only picked up on putative integration events that persisted after multiple cell replications. That is to say, the scientists were not able to detect integration events that may have occurred, but then died off immediately.

    At the moment, no one knows how many integration events might be occurring, or what effect that would have on patients. “The unknowns are just exponential,” says McKernan.

    The cancer cell line experiment can be said to be “a microcosm of genome integration of contaminated DNA,” said Japanese molecular oncology scientist Hiroshi Arakawa, in his own analysis of McKernan and Dr Kämmerer’s experiment, published to his popular science blog on which he shares critical views on Covid vaccine safety.

    Akira calls the two possible integrations observed in Dr Kämmerer’s experiment a “major advance” laying the ground for further experimentation. “What happens in cultured cells can also occur in normal cells, and a wide variety of abnormalities can occur depending on the site of genome integration,” such as “the induction of cancer or malignant transformation,” he wrote (translated from Japanese to English).

    LNPs deliver contaminant DNA straight to the cells

    A key assumption underlying claims that mRNA Covid vaccine contamination cannot enter the cell nucleus, and cannot genomically integrate with host DNA, is that the contamination will never make it into dividing cells, which would be required for integration to occur.

    This is based on the assumption that the LNPs containing both mod-RNA and contaminant DNA mostly stay in the muscle at the injection site. As muscle cells do not divide, there’s no problem, the logic goes.

    This is misleading, however, as Pfizer’s own biodistribution data shows that the LNPs enter the blood and every major organ system, including the ovaries, as mentioned above. While it is true that muscle cells don’t divide, LNPs distributed around the body can transfect any number of dividing cells in various organ systems.


    Table 4-2. shows biodistribution of LNPs, Pfizer Nonclinical Evaluation Report, 2021
    From there, it’s only a matter of time before the LNP contents get into the cell nucleus, says McKernan. “In any dividing cell, the nucleus dissolves. So, when people say the DNA can get into the cytoplasm [inside the cell membrane] but won't get into the nucleus, well, in any dividing cell, it will end up getting into the nucleus.”

    It is possible that the dissolution of the cell nucleus during division is the mechanism underlying McKernan and Dr Kämmerer’s observed passaging of contaminant DNA, but further research will be required to confirm or disprove this hypothesis.

    Because of the effectiveness of LNPs in delivering their contents into cells, McKernan, Dr Buckhaults and Dr Speicher have questioned the suitability of the current regulatory limits on contaminant DNA in vaccines, which were set prior to the introduction of LNP technology in vaccines.

    Regulators unconcerned

    I sent McKernan’s Substack article documenting the new DNA integration findings to Australia’s drug regulator, the Therapeutic Goods Administration, for comment.

    The TGA did not address the new findings, but a spokesperson from the TGA responded,

    “The Department of Health and Aged Care has every confidence in the safety, quality and efficacy of the various approved COVID-19 vaccines for use in Australia. The TGA’s assessment of all vaccines is based upon high quality evidence, including studies and reviews published in peer-reviewed scientific and clinical journals.”

    However, when asked previously to provide evidence for its position that Covid vaccines pose no risk of DNA integration, the TGA provided no peer-reviewed scientific evidence to support its claims.

    Instead, the TGA provided links to a Mayo Clinic fact page with no scientific citations, an article by the discredited RMIT FactLab, and a scientific commentary article suggesting that in vitro findings cannot be generalised.

    Furthermore, TGA has not been forthcoming with the evidence it does hold. When asked to release Covid vaccine batch testing results under Freedom of Information, the regulator provided all 74 pages - fully redacted.

    In the US, the Food and Drug Administration (FDA) denied that contaminant DNA in the mRNA vaccines can enter the nucleus or pose any threat to patients’ genomic DNA, in a response to concerns raised by Florida Surgeon General, Dr Joseph A. Ladapo in December of last year.

    Additionally, the FDA misleadingly refuted the presence of SV40 proteins in the vaccines, when in fact Dr Ladapo raised concerns over the presence of an SV40 enchancer sequence in the Pfizer vaccine, as confirmed by Health Canada and numerous independent laboratories.

    Such ham-fisted mischaracterisation of a gene therapy sequence by the FDA is suggestive of either gross incompetence, or a disinformation play. Both are concerning.

    Science journalist Maryanne Demasi reported, in November last year, that the FDA shut down her enquiries into the DNA contamination matter, refusing to confirm if it found levels of DNA that exceeded acceptable levels, or if it was investigating further.

    The presence of contamination has been officially acknowledged by the European Medicines Agency (EMA) and Health Canada, with the latter also acknowledging the presence of the SV40 enhancer sequence, though both regulators deny that the amounts exceed regulatory limits, or that the DNA contamination poses any risk.

    ‘No excuse’ for ignoring ‘screaming hot signal’

    Instead of denying excessive DNA levels and deferring to manufacturers’ reported test results, regulators should run their own qPCR testing on batch lots, says McKernan.

    Then, “they would see what everyone else is seeing, which is that sometimes the CT scores come out as low as 13… that’s a screaming hot signal.”

    “As a reference, the Covid test would call people positive at 33-35,” McKernan explains. “That’s a million-fold difference (20 CTs). A million-fold less Covid RNA and you're positive and quarantined. But you can inject a million-fold more past your mucosa?”

    There’s “no excuse” for regulators to not sequence every vaccine lot, says McKernan, when the costs for doing so have dropped dramatically in recent years.

    “DNA sequencing costs have dropped 100,000 fold in the last decade. They have relaxed the DNA contamination limits 1000-fold in this time frame. It likely only costs $1,000 in reagents for millions-to-billions of dollars worth of product.”


    Source: National Human Genome Research Institute
    DNA sequencing by regulatory agencies is important not just for measuring quantities, says McKernan, but also for determining the type of DNA contamination.

    “Not all DNA is created equal. Some is designed to replicate - when it gets into a cell, it can make more of itself. It's a massive loophole in the regulations that they don't do sequencing. But it's never been cheaper. You can precisely know the nature of the DNA in every single vial.”

    Scientists pick up regulators’ slack

    In the absence of any regulatory appetite for investigating the risks of DNA contamination in the mRNA Covid shots, and particularly the risk of genomic integration, independent scientists have taken the baton.

    “We are writing up our findings and will publish a preprint soon,” says McKernan, who is planning further testing in partnership with Dr Kämmerer. “We’re doing more experiments first. We need to sequence deeper to find out if the integration events are in chromosomal or extra-chromosomal DNA.”

    Dr Buckhaults is also running his own experiment, calling for de-identified samples of tumours or fresh blood from pathology and hematology labs. These samples will be tested for the presence of plasmid DNA contamination, with whole genome sequencing to then be carried out on positive samples to identify genomic integration sites.

    In an email outlining his experiment, Dr Buckhaults told me that he intends to report his findings in a peer-reviewed publication, predicting that the work could take “a few months to a year,” depending on how fast samples come in.

    “I am hopeful to prove my concerns are unwarranted by accumulating a lot of negative data, and of course negative data takes the most time to collect,” he said.

    McKernan says he is aware of other labs running tests for contaminant plasmid DNA integration, but cannot disclose the details at present.

    Decentralisation the future of science?

    McKernan says he has experienced some pushback for publishing his methods and findings in real time via Substack, X, and preprints. But, he believes that making his data available as quickly as possible is a way for the field of science to regain public trust.

    “Many will criticize our disclosure of preliminary findings but we feel this is an insult to the intelligence of the average person,” says McKernan.

    “It's a form of scientific elitism that implies people can't handle the truth and will be scared like sheep if given a glimpse of how the true scientific process is performed. Scientists are 90% of the time wrong but only publish the times when they are right. There is no journal of negative results.“

    In light of the prospect that most published research findings are false (as famously asserted in a 2005 article by Professor John Ioannidis), McKernan questions the value of peer-review, instead favouring replication or refutation in the real world.


    Source: X
    For this reason, McKernan says he has not prioritised peer-reviewed publication for his DNA contamination findings, but is rather focusing on conducting more experiments and releasing the data as he goes - even when it’s incomplete, or requires further experimentation.

    “We were not expecting to find any integration events at this depth of coverage, but they are evident to anyone who downloads our public reads. To not speak to obvious evidence in such data would be irresponsible even when such evidence doesn't 100% answer a given question,” says McKernan.

    Dr Buckhaults takes a somewhat different view. After sharing his initial plasmid DNA contamination findings in a South Carolina Senate hearing in September last year, the video recording broke the internet.

    Believing the hearing to have been private, Dr Buckhaults was alarmed that the widespread distribution of his testimony may have caused “unintended, harmful side effects.” He requested that YouTube take down his testimony video, which is now defunct.


    Source: X
    In our correspondence, Dr Buckhaults stressed that while more research is warranted, he is of the opinion that the public “should not overreact to the news of the plasmid DNA contamination. It's serious enough that scientists need to hustle and figure out if it's causing any health problems now or down the road, but it's not cause for the general public to be alarmed.”

    But, “The reality is that`transfection experiments with contaminated DNA' have been carried out on vast numbers of people around the world in the name of vaccination,” writes Arakawa.

    Perhaps the experiment participants will be the ones to decide if they should be alarmed, or not.

    The FDA was contacted for comment about Dr Kämmerer and McKernan’s new findings, but they did not respond by publication deadline. This article will be updated if comment is received.

    View Kevin McKernan’s write up of his DNA integration experiment (in partnership with Dr Kämmerer) here. Scroll down for links to sequencing data files.

    Pathology and hematology labs wishing to send samples to Dr Buckhaults are invited to contact him at the University of South Carolina.

    Update 23 March 2024: This article was edited to add mention of the Dr David Speicher et al. finding of “billions to hundreds of billions of DNA molecules per dose” of the mRNA vaccines, and the scientists’ concerns that regulatory limits on DNA contamination have not taken LNP transfection into account.


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    1
    From an article I wrote for Umbrella News on this topic last year:

    The TGA maintains that allegations put forward in the case about the potential for mRNA vaccines to alter the recipient’s DNA are unfounded. A spokesperson for the TGA told Umbrella News,

    “COVID-19 vaccines do not alter a person’s DNA. The mRNA in the vaccines does not enter the nucleus of cells and is not integrated into the human genome. Thus, the mRNA does not cause genetic damage or affect the offspring of vaccinated individuals.”

    “The TGA continues to monitor the scientific literature associated with the SARS – CoV-2 virus and the various COVID-19 vaccines approved for use in Australia.”

    With reference to the specific studies cited in the case materials, the TGA pointed Umbrella News to an RMIT ABC Fact Check post from 2022 purporting to ‘debunk’ claims that mRNA jabs are genotoxic. This is the same site that ‘debunked’ claims that COVID vaccines can cause menstrual disruption, before peer-reviewed scientific studies proved that they can and do (the post has not been corrected).

    As evidence that it is “well established” that vaccine mRNA and protein do not enter the nucleus, the TGA provided a link to a Mayo Clinic fact page which provides no studies or scientific evidence in support of its claims.

    The TGA did provide one commentary article published in a scientific journal which pointed out that the in vitro liver cell line study cannot be extrapolated to generalise about in vivo findings (in a human, not a dish) without further research being undertaken.

    Additionally, RMIT FactLab was suspended by Facebook in August 2023 after an uproar over its blatantly biased and factually dubious ‘fact checking’ of media articles relating to the Voice referendum campaign. It also transpired that RMIT FactLab had falsely represented its accreditation with the International Fact-Checking Network as current, when it had in fact lapsed.


    https://news.rebekahbarnett.com.au/p/dna-contamination-in-covid-vaccines
    DNA contamination in Covid vaccines DOES get into human cells, new evidence shows It also appears that the contamination enters the cell nucleus and integrates with human DNA Rebekah Barnett Regulators and fact checkers claim that plasmid DNA contamination in the mRNA Covid vaccines can’t change your genomic DNA, but new evidence suggests that it actually can. The fact checkers assert that DNA contamination poses no risk to your genomic DNA because your body will naturally destroy any contaminant DNA before it even gets into the cells. Even if the contaminant DNA could get into cells, there’s no way it can enter the cell nucleus, where genomic integration events occur, they say. And even if the contaminant DNA could enter the nucleus, which it can’t, it still couldn’t genomically integrate unless specific enzymes are present, they say. However, results from independent lab testing conducted on ovarian cancer cell lines show that contaminant DNA from Pfizer’s Covid vaccine not only crossed into the cells, but that it survived multiple cell divisions. This is suggestive that the contaminant DNA is able to transfect (enter) the cell nucleus, and that it integrated with the human cell DNA. TLDR 1. Scientists claim that Pfizer vaccine contaminant DNA has been detected in ovarian cancer cell line DNA, but they do not yet know if it’s chromosomal (heritable) or extra-chromosomal DNA (not heritable) 2. This is an in vitro (in a lab dish) finding, and needs to be replicated in vivo (in a human patient) 3. As the finding is specific to cancer cell lines, it is not generalisable, but scientists say it may give an indication of what cancer patients in remission could experience after mRNA Covid vaccination 4. This finding calls into question fact checker claims that mRNA Covid vaccine DNA contamination can't enter cells, can't enter the nucleus, and cannot integrate with human DNA. Last year, Boston-based genomics scientist Kevin McKernan made the shocking discovery that the mRNA Covid vaccines are contaminated with excessive levels of plasmid DNA, an artefact of the vaccine production process. McKernan’s findings were soon confirmed by multiple independent labs around the world for both the Pfizer and Moderna mono- and bi-valent vaccines, including lots approved for children, with one Canadian study led by Dr David Speicher concluding that there are “billions to hundreds of billions of DNA molecules per dose.” Scientists including McKernan, University of South Carolina cancer genomics scientist Dr Phillip Buckhaults, and Dr Wafik El-Diery, head of the Cancer Centre at Brown University, expressed concerns that fragments of plasmid DNA contamination could cause adverse events, autoimmune problems and cancers in some patients. But perhaps most significantly, there is also a theoretical risk of the contaminant DNA integrating with patients’ chromosomal DNA and modifying the human genome. This is of particular concern with the Pfizer vaccine, which contains an SV40 enhancer sequence, used in gene therapies “to drive DNA into the nucleus,” explains McKernan. While regulators have taken a ‘wait and see’ approach, independent scientists, including McKernan, have been more proactive, initiating experiments testing for evidence of genomic integration. Now, the first results are in. In an experiment conducted together with German molecular biologist Dr Ulrike Kämmerer, McKernan has detected vaccine contaminant DNA in ovarian cancer cell lines treated with Pfizer’s Covid vaccine. The scientists found a chimeric combination of human ovarian cell line DNA and spike sequence DNA derived from the contaminating plasmid at at least one, and possibly two sites. “If anything, this work has put to bed the question regarding if this contaminant DNA gets into the cell, and the chimeric human and contaminant spike DNA sequences imply it has entered the nucleus,” McKernan says. “The PCR and sequencing data both demonstrate the vaccine is getting into the cell and surviving cell passaging. It is likely bioactive and being partially replicated.” To reach this finding, Dr Kämmerer first treated ovarian cancer cell lines with mRNA Covid vaccines, using cells treated with AstraZeneca and Janssen vaccines as controls. The cells were then ‘passaged’, meaning they were left to divide and replicate numerous times. This has the effect of “rinsing away residual vaccine,” explains McKernan. Immunohistochemistry (IHC) was then performed, a staining process that Dr Kämmerer used to detect levels of spike protein expression produced by the vaccine modified-RNA. This was to confirm that the lipid nanoparticles (LNPs) carrying mod-RNA and plasmid DNA contamination “did their job and delivered the payload,” says McKernan. Measuring how many cells expressed spike protein also allowed the scientists to determine how much of the vaccine to treat the cells with. Immunohistochemistry performed with Pfizer top left, AstraZeneca top right as a control. Source: Kevin McKernan’s Substack Cell lines were then sent in cold storage to McKernan’s Boston lab, where his team used qPCR to screen which samples to sequence the cell line DNA. “What we found is, [contaminant] DNA that is getting transfected into ovarian cancer cell lines is replicating in the cells,” says McKernan, noting that the ratio of vaccine contaminant DNA to human cell DNA was “higher than we expected.” Chimeric sequences of human and vaccine contaminant DNA were detected at two sites: chromosomes 9 and 12, with the evidence for the latter being the strongest. “But we don't know if it's extra-chromosomal or whether it's chromosomal because of the Illumina (short read) method we used to sequence,” explains McKernan. Source: Kevin McKernan’s Substack Extra-chromosomal DNA is not part of the chromosome, and is therefore less likely to replicate and to be heritable. Chromosomal DNA, on the other hand, is heritable and more likely to be replicated. A third category, mitochondrial DNA, is heritable, but only from the maternal line. You can read a detailed account of methods and findings via McKernan’s Substack article, ‘Vaccine targeted qPCR of Cancer Cell Lines treated with BNT162b2.’ ‘Major advance,’ but clinical implications are limited McKernan emphasises that these findings cannot be generalised, stating that “it is too early to make comments on the clinical implications.” “The study is performed in ovarian cancer cell lines. It is not performed in patient cells, but this is a proxy for what might happen in an ovarian cancer patient who's in remission,” says McKernan, especially as there is evidence that the LNPs go to the ovaries. The risk for patients in this scenario is that integration events with contaminant DNA might cause aberrant cell growth, which poses a risk to immune suppression of new cancer cells. McKernan notes that his experiment only picked up on putative integration events that persisted after multiple cell replications. That is to say, the scientists were not able to detect integration events that may have occurred, but then died off immediately. At the moment, no one knows how many integration events might be occurring, or what effect that would have on patients. “The unknowns are just exponential,” says McKernan. The cancer cell line experiment can be said to be “a microcosm of genome integration of contaminated DNA,” said Japanese molecular oncology scientist Hiroshi Arakawa, in his own analysis of McKernan and Dr Kämmerer’s experiment, published to his popular science blog on which he shares critical views on Covid vaccine safety. Akira calls the two possible integrations observed in Dr Kämmerer’s experiment a “major advance” laying the ground for further experimentation. “What happens in cultured cells can also occur in normal cells, and a wide variety of abnormalities can occur depending on the site of genome integration,” such as “the induction of cancer or malignant transformation,” he wrote (translated from Japanese to English). LNPs deliver contaminant DNA straight to the cells A key assumption underlying claims that mRNA Covid vaccine contamination cannot enter the cell nucleus, and cannot genomically integrate with host DNA, is that the contamination will never make it into dividing cells, which would be required for integration to occur. This is based on the assumption that the LNPs containing both mod-RNA and contaminant DNA mostly stay in the muscle at the injection site. As muscle cells do not divide, there’s no problem, the logic goes. This is misleading, however, as Pfizer’s own biodistribution data shows that the LNPs enter the blood and every major organ system, including the ovaries, as mentioned above. While it is true that muscle cells don’t divide, LNPs distributed around the body can transfect any number of dividing cells in various organ systems. Table 4-2. shows biodistribution of LNPs, Pfizer Nonclinical Evaluation Report, 2021 From there, it’s only a matter of time before the LNP contents get into the cell nucleus, says McKernan. “In any dividing cell, the nucleus dissolves. So, when people say the DNA can get into the cytoplasm [inside the cell membrane] but won't get into the nucleus, well, in any dividing cell, it will end up getting into the nucleus.” It is possible that the dissolution of the cell nucleus during division is the mechanism underlying McKernan and Dr Kämmerer’s observed passaging of contaminant DNA, but further research will be required to confirm or disprove this hypothesis. Because of the effectiveness of LNPs in delivering their contents into cells, McKernan, Dr Buckhaults and Dr Speicher have questioned the suitability of the current regulatory limits on contaminant DNA in vaccines, which were set prior to the introduction of LNP technology in vaccines. Regulators unconcerned I sent McKernan’s Substack article documenting the new DNA integration findings to Australia’s drug regulator, the Therapeutic Goods Administration, for comment. The TGA did not address the new findings, but a spokesperson from the TGA responded, “The Department of Health and Aged Care has every confidence in the safety, quality and efficacy of the various approved COVID-19 vaccines for use in Australia. The TGA’s assessment of all vaccines is based upon high quality evidence, including studies and reviews published in peer-reviewed scientific and clinical journals.” However, when asked previously to provide evidence for its position that Covid vaccines pose no risk of DNA integration, the TGA provided no peer-reviewed scientific evidence to support its claims. Instead, the TGA provided links to a Mayo Clinic fact page with no scientific citations, an article by the discredited RMIT FactLab, and a scientific commentary article suggesting that in vitro findings cannot be generalised. Furthermore, TGA has not been forthcoming with the evidence it does hold. When asked to release Covid vaccine batch testing results under Freedom of Information, the regulator provided all 74 pages - fully redacted. In the US, the Food and Drug Administration (FDA) denied that contaminant DNA in the mRNA vaccines can enter the nucleus or pose any threat to patients’ genomic DNA, in a response to concerns raised by Florida Surgeon General, Dr Joseph A. Ladapo in December of last year. Additionally, the FDA misleadingly refuted the presence of SV40 proteins in the vaccines, when in fact Dr Ladapo raised concerns over the presence of an SV40 enchancer sequence in the Pfizer vaccine, as confirmed by Health Canada and numerous independent laboratories. Such ham-fisted mischaracterisation of a gene therapy sequence by the FDA is suggestive of either gross incompetence, or a disinformation play. Both are concerning. Science journalist Maryanne Demasi reported, in November last year, that the FDA shut down her enquiries into the DNA contamination matter, refusing to confirm if it found levels of DNA that exceeded acceptable levels, or if it was investigating further. The presence of contamination has been officially acknowledged by the European Medicines Agency (EMA) and Health Canada, with the latter also acknowledging the presence of the SV40 enhancer sequence, though both regulators deny that the amounts exceed regulatory limits, or that the DNA contamination poses any risk. ‘No excuse’ for ignoring ‘screaming hot signal’ Instead of denying excessive DNA levels and deferring to manufacturers’ reported test results, regulators should run their own qPCR testing on batch lots, says McKernan. Then, “they would see what everyone else is seeing, which is that sometimes the CT scores come out as low as 13… that’s a screaming hot signal.” “As a reference, the Covid test would call people positive at 33-35,” McKernan explains. “That’s a million-fold difference (20 CTs). A million-fold less Covid RNA and you're positive and quarantined. But you can inject a million-fold more past your mucosa?” There’s “no excuse” for regulators to not sequence every vaccine lot, says McKernan, when the costs for doing so have dropped dramatically in recent years. “DNA sequencing costs have dropped 100,000 fold in the last decade. They have relaxed the DNA contamination limits 1000-fold in this time frame. It likely only costs $1,000 in reagents for millions-to-billions of dollars worth of product.” Source: National Human Genome Research Institute DNA sequencing by regulatory agencies is important not just for measuring quantities, says McKernan, but also for determining the type of DNA contamination. “Not all DNA is created equal. Some is designed to replicate - when it gets into a cell, it can make more of itself. It's a massive loophole in the regulations that they don't do sequencing. But it's never been cheaper. You can precisely know the nature of the DNA in every single vial.” Scientists pick up regulators’ slack In the absence of any regulatory appetite for investigating the risks of DNA contamination in the mRNA Covid shots, and particularly the risk of genomic integration, independent scientists have taken the baton. “We are writing up our findings and will publish a preprint soon,” says McKernan, who is planning further testing in partnership with Dr Kämmerer. “We’re doing more experiments first. We need to sequence deeper to find out if the integration events are in chromosomal or extra-chromosomal DNA.” Dr Buckhaults is also running his own experiment, calling for de-identified samples of tumours or fresh blood from pathology and hematology labs. These samples will be tested for the presence of plasmid DNA contamination, with whole genome sequencing to then be carried out on positive samples to identify genomic integration sites. In an email outlining his experiment, Dr Buckhaults told me that he intends to report his findings in a peer-reviewed publication, predicting that the work could take “a few months to a year,” depending on how fast samples come in. “I am hopeful to prove my concerns are unwarranted by accumulating a lot of negative data, and of course negative data takes the most time to collect,” he said. McKernan says he is aware of other labs running tests for contaminant plasmid DNA integration, but cannot disclose the details at present. Decentralisation the future of science? McKernan says he has experienced some pushback for publishing his methods and findings in real time via Substack, X, and preprints. But, he believes that making his data available as quickly as possible is a way for the field of science to regain public trust. “Many will criticize our disclosure of preliminary findings but we feel this is an insult to the intelligence of the average person,” says McKernan. “It's a form of scientific elitism that implies people can't handle the truth and will be scared like sheep if given a glimpse of how the true scientific process is performed. Scientists are 90% of the time wrong but only publish the times when they are right. There is no journal of negative results.“ In light of the prospect that most published research findings are false (as famously asserted in a 2005 article by Professor John Ioannidis), McKernan questions the value of peer-review, instead favouring replication or refutation in the real world. Source: X For this reason, McKernan says he has not prioritised peer-reviewed publication for his DNA contamination findings, but is rather focusing on conducting more experiments and releasing the data as he goes - even when it’s incomplete, or requires further experimentation. “We were not expecting to find any integration events at this depth of coverage, but they are evident to anyone who downloads our public reads. To not speak to obvious evidence in such data would be irresponsible even when such evidence doesn't 100% answer a given question,” says McKernan. Dr Buckhaults takes a somewhat different view. After sharing his initial plasmid DNA contamination findings in a South Carolina Senate hearing in September last year, the video recording broke the internet. Believing the hearing to have been private, Dr Buckhaults was alarmed that the widespread distribution of his testimony may have caused “unintended, harmful side effects.” He requested that YouTube take down his testimony video, which is now defunct. Source: X In our correspondence, Dr Buckhaults stressed that while more research is warranted, he is of the opinion that the public “should not overreact to the news of the plasmid DNA contamination. It's serious enough that scientists need to hustle and figure out if it's causing any health problems now or down the road, but it's not cause for the general public to be alarmed.” But, “The reality is that`transfection experiments with contaminated DNA' have been carried out on vast numbers of people around the world in the name of vaccination,” writes Arakawa. Perhaps the experiment participants will be the ones to decide if they should be alarmed, or not. The FDA was contacted for comment about Dr Kämmerer and McKernan’s new findings, but they did not respond by publication deadline. This article will be updated if comment is received. View Kevin McKernan’s write up of his DNA integration experiment (in partnership with Dr Kämmerer) here. Scroll down for links to sequencing data files. Pathology and hematology labs wishing to send samples to Dr Buckhaults are invited to contact him at the University of South Carolina. Update 23 March 2024: This article was edited to add mention of the Dr David Speicher et al. finding of “billions to hundreds of billions of DNA molecules per dose” of the mRNA vaccines, and the scientists’ concerns that regulatory limits on DNA contamination have not taken LNP transfection into account. To support my work, make a one-off contribution to DDU via my Kofi account and/or subscribe. Thanks! Follow me on X Follow me on Instagram 1 From an article I wrote for Umbrella News on this topic last year: The TGA maintains that allegations put forward in the case about the potential for mRNA vaccines to alter the recipient’s DNA are unfounded. A spokesperson for the TGA told Umbrella News, “COVID-19 vaccines do not alter a person’s DNA. The mRNA in the vaccines does not enter the nucleus of cells and is not integrated into the human genome. Thus, the mRNA does not cause genetic damage or affect the offspring of vaccinated individuals.” “The TGA continues to monitor the scientific literature associated with the SARS – CoV-2 virus and the various COVID-19 vaccines approved for use in Australia.” With reference to the specific studies cited in the case materials, the TGA pointed Umbrella News to an RMIT ABC Fact Check post from 2022 purporting to ‘debunk’ claims that mRNA jabs are genotoxic. This is the same site that ‘debunked’ claims that COVID vaccines can cause menstrual disruption, before peer-reviewed scientific studies proved that they can and do (the post has not been corrected). As evidence that it is “well established” that vaccine mRNA and protein do not enter the nucleus, the TGA provided a link to a Mayo Clinic fact page which provides no studies or scientific evidence in support of its claims. The TGA did provide one commentary article published in a scientific journal which pointed out that the in vitro liver cell line study cannot be extrapolated to generalise about in vivo findings (in a human, not a dish) without further research being undertaken. Additionally, RMIT FactLab was suspended by Facebook in August 2023 after an uproar over its blatantly biased and factually dubious ‘fact checking’ of media articles relating to the Voice referendum campaign. It also transpired that RMIT FactLab had falsely represented its accreditation with the International Fact-Checking Network as current, when it had in fact lapsed. https://news.rebekahbarnett.com.au/p/dna-contamination-in-covid-vaccines
    NEWS.REBEKAHBARNETT.COM.AU
    DNA contamination in Covid vaccines DOES get into human cells, new evidence shows
    It also appears that the contamination enters the cell nucleus and integrates with human DNA
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  • CMNnews -- Your Credible Medical News Network -- Update 27th February 2024
    From Global sources -- Updated Twice Weekly -- CMNNEWS -- We roam the planet for the best Medical News Stories

    CMNnews
    THE DOCTORS

    MONKEY NOT SEE — MONKEY NOT HEAR — MONKEY NOT SPEAK


    HISTORIC AUSTRALIAN SUPREME COURT DECISION

    STATE GOVERNMENT FOUND “ACTED UNLAWFULLY”

    IN REGARD TO VACCINE MANDATES ON POLICE AND AMBULANCE WORKERS

    Supreme Court bombshell: Queensland’s mandatory Covid vaccine orders ‘unlawful’

    Excerpts: Dozens of police and health workers have won a mammoth legal battle over mandatory Covid vaccination orders.

    Vanda Carson court reporter Courier Mail Newspaper Queensland, Australia

    2 min read

    In a 115-page decision handed down by Justice Glenn Martin on Tuesday he declared police commissioner Katarina Carroll’s direction for mandatory Covid-19 vaccination issued in December 2021 was unlawful under the Human Rights Act and banned her from taking any steps to enforce the direction.

    He also ruled that a similar order by John Wakefield, the director general of Queensland Health’s equivalent vaccination policy “is of no effect” and Mr Wakefield be blocked from forcing paramedics to have the injection.

    The workers did not have to be vaccinated while their legal fight was underway.

    Ms Carroll and Mr Wakefield are also banned from disciplining any of the paramedics and police officers.

    “I am not satisfied that the (police) Commissioner has demonstrated that she gave proper consideration to the human rights that might have been affected by her decisions,” Justice Martin said in relation to the police staff.

    “I do not accept that the Commissioner had … considered whether the decision would be compatible with human rights,” he noted in his 115-page decision.

    “By failing to give proper consideration, the making of each of those decisions was unlawful.

    “Despite the revocation of the QPS Directions, a finding of unlawfulness is still available.”

    Link: https://www.couriermail.com.au/truecrimeaustralia/police-courts-qld/supreme-court-bombshell-qlds-mandatory-covid-vaccine-orders-unlawful/news-story/4dcc6ca18dae261249fd7988642192fb

    Share CMNNews -- The Credible Medical News Network

    Update Article: Supreme Court bombshell: Qld’s mandatory Covid vaccine orders ‘unlawful’

    Excerpts: Dozens of police and health workers including paramedics have won a mammoth legal battle over mandatory ­vaccination orders after the Supreme Court declared they were unlawful.

    A spokeswoman for the Nurses’ Professional Association of Queensland (NPAQ) said the Supreme Court ruling “ highlighted how Queensland Health has violated thousands of healthcare workers’ rights”.

    The association highlighted that during a workforce crisis there were members who were stood due to the vaccine mandate who are dying to return to work.

    “We have nurses and midwives sitting at home during a workforce crisis and the healthcare system’s unlawful decisions are directly to blame,” the spokeswoman said.

    “NPAQ is currently liaising with our legal team to explore legal avenues for our members in light of today’s Supreme Court outcome.”

    https://www.couriermail.com.au/truecrimeaustralia/police-courts-qld/supreme-court-bombshell-qlds-mandatory-covid-vaccine-orders-unlawful/news-story/4dcc6ca18dae261249fd7988642192fb

    COVID-19 vaccine mandates 'unlawful' for emergency services, court finds

    The court on Tuesday delivered its judgments in three lawsuits brought by 86 parties against Queensland Police Service and Queensland Ambulance Service for their directions to workers issued in 2021 and 2022.

    The court found Police Commissioner Katarina Carroll failed to give proper consideration to human rights relevant to the decision to issue the vaccine mandate.

    “The court also found the directions limited the human rights of workers because they were required to undergo a medical procedure without full consent ….”

    Australian Senate finally acknowledge excess deaths are concerning : Letter from Australian Senator Ralph Babet

    SENATOR RALPH BABET — IS THIS THE GREATEST SENATE DECISION IN HISTORY? TWO MINUTE VIDEO



    JIM FERGUSON – “THIS IS GENOCIDE – MURDER OF MILLIONS AND POSSIBLY BILLIONS OF PEOPLE” – “THE PRIME MINISTER COULD BE INVOLVED” -- “THESE ARE CRIMES AGAINST HUMANITY”

    “Explosive allegations against top Government officials in the UK Government update. As Member of Parliament Andrew Bridgen prepares to present evidence of potential criminal conduct involving Prime Minister Rishi Sunak and his cabinet to London's Metropolitan Police Commissioner Mark Rowley, we explore the mindset of others who might be implicated in alleged widespread wrongdoing, including potential mass genocide and profiteering. Will they now do the right thing and blow the lid on whats really been going on! If the gatekeepers in our Security Services and Police are compromised or complicit in what is arguably the greatest potential crime against humanity of all time then all bets are off as to what happens next.”

    https://twitter.com/i/status/1761505188056072263

    DR DAVID MARTIN EXPLAINS WHO THEY ARE AND HOW THEY ARE DOING THIS TO US


    “THEY WERE CONVICTED OF ANTI-TRUST CRIMES”

    “THIS IS A CRIMINAL CONSPIRACY”

    “WHO IS MOVING THE STICK – WELLCOME, GATES AND ROCKEFELLER”

    “THIS IS A VIOLATION OF SWISS LAW”

    Dr. David Martin Reveals Who Is Pulling the Strings Behind the World Health Organization

    Who are “THEY”? “We have to name the names” in the worst miscarriage of medical science in history. Is it the World Health Organization? Dr. David Martin says Tedros is just a puppet with a “giant stick up his ass, which is what’s making his mouth move…

    18 days ago · 446 likes · 136 comments · The Vigilant Fox

    BILL GATES DONATION TO WORLD HEALTH ORGANIZATION


    JIM FERGUSON INTERVIEWS ANDREW BRIDGEN --

    “Exclusive Breaking News: Evidence to be presented that criminal activity has been committed by the very top of Government in the UK. Rishi Sunak British Prime Minister may face a criminal investigation and face potential criminal charges of the most egregious kind. British MP Andrew Bridgen has written to Mark Rowley Commissioner of the Metropolitan Police and the most senior of Police officers to have a three hour meeting where experts and whistle blowers will lay out the evidence where potential criminal activity has been conducted by the very top of Government and the civil service in the UK Parliament has been deliberately misled over the vaccine contracts. This matter may be taken to Parliamentary standards in addition to the presentation of evidence to the Police and the Security services. "heads of governments around the world and others below them have engaged in what is tantamount to treason against the public" Office of National Statistics (ONS) figures on Excess Deaths are being covered up. "there is a huge coverup going on" In August 2019 a member of the security services stated that there was a pandemic coming and not to take any of the vaccines. Bill gates and Rishi Sunak invested heavily into the Pharma companies like Pfizer and Moderna prior to the pandemic. Did they have insider knowledge about what was being planned in a coming pandemic! 75% of congressmen and woman in the United States have investments in Big Pharma. A Pfizer executive stated that a senator could be bought for $10,000. The journalists are complicit in the cover up. Main Stream Media are bought and paid for. A court case has been launched against the former health secretary Matt Hancock for defamation against Andrew Bridgen and this will take place in the Royal Court of Justice.”

    https://twitter.com/i/status/1761393940874293335

    THESE EVIL PEOPLE ARE COMING AFTER OUR PETS – YOUR DOGS AND CATS – A SECURITY CHIEF WARNED “DO NOT TAKE THE VACCINE” – “THE PRIME MINISTER OF THE UK, RISHI SUNAK, INVESTED HALF A BILLION DOLLARS INTO MODERNA TWO TO THREE YEARS BEFORE COVID OCCURRED” – “HE MUST HAVE HAD PRIOR KNOWLEDGE”

    https://rumble.com/v4ew676-these-evil-monsters-are-coming-after-our-pets.html


    JIM FERGUSON ON TWITTER

    @JimFergusonUK

    “British PM and #WEF2030Agenda devotee #Sunak invested $500 million of his private funds into Moderna through a company called Thelema Partners in a notorious tax haven in the Caymen Islands. Afterwards he stated in parliament that the vaccine was "safe and effective" while then going on to roll out further permissions for Moderna to set up further vaccine producing interests within the UK. Did he use his position as Prime Minister to make massive personal profits while knowingly or even unknowingly causing harm to the British people and has he broken the National Security Act which states "if you're working in secret for a foreign power to use or abuse your knowledge in a way that causes harm to our citizens you will be a criminal." Former Head of MI6 Sir Alex Younger.”

    2024 Is the Last Year of Free Speech and Democracy in the Western World

    https://www.paulcraigroberts.org/2024/02/19/2024-is-the-last-year-of-free-speech-and-democracy-in-the-western-world/


    To Understand The Globalists We Must Understand Their Psychopathic Religion

    https://alt-market.us/to-understand-the-globalists-we-must-understand-their-psychopathic-religion/

    TWO BRAVE AND COURAGEOUS DOCTORS

    #141 - Dr Charles Hoffe, A Persecuted Ethical Doctor Or Dangerous Misinformation Spreader?

    FREEDOM - LIBERTY - HAPPINESS SUPPORT DOC MALIK About this conversation - Dr Charles Hoffe is a family doctor who lives and works in British Columbia, Canada. He has worked in general practice and emer…

    14 days ago · 34 likes · 5 comments · Doc Malik

    New Zealand COVID-19 Vaccine Victims Documentary: "Silent No More" (June 2023)

    VIDEO - New Zealand COVID-19 Vaccine Victims Documentary: "Silent No More" (June 2023)

    VIDEO - New Zealand COVID-19 Vaccine Victims Documentary: "Silent No More" (June 2023…

    14 days ago · 122 likes · 57 comments · Dr. William Makis MD

    LIST OF LAWYERS NOW AVAILABLE FOR LAWSUITS ON COVID VACCINE INJURY

    https://deeprootsathome.com/list-of-attorneys-worldwide-now-available-for-lawsuits/


    Kaboom! — Renowned Neurologist and Thai Red Cross Emerging Infectious Diseases Health Science Centre Lead Prof. Dr. Thiravat Hemachudha Exposes Vaccine-Linked White Clots on Thailand's Popular TV3

    "We've just seen this in the last 2 years... but we didn’t see this before the vaccines. The doctor noticed this between two years to one year ago, in about 50% of the patients,"

    Kaboom! Renowned Neurologist and Thai Red Cross Emerging Infectious Diseases Health Science Centre Lead Prof. Dr. Thiravat Hemachudha Exposes Vaccine-Linked White Clots on Thailand's Popular TV3

    It’s taking a long time folks, but the worms are crawling out of the cans, and corrupt institutions and politicians are scrambling to seal them back in! Perhaps due to a significant decrease in mRNA vaccine sales influencing pharmaceutical companies…

    18 days ago · 103 likes · 30 comments · Aussie17

    mRNA VACCINE SHEDDING OF SPIKE PROTEIN

    As Dr. Kory points out, “COVID “vaccines” are gene therapy products as defined in the FDA’s 2015 document on Gene Product Shedding Studies and all other gene therapy products on the market list shedding as a risk in their [package] insert (Luxterna, Roctavian, Zolgensma) and shed from 7 days to 6 months.”

    phillip.altman’s Substack

    mRNA VACCINE SHEDDING OF SPIKE PROTEIN There has been considerable concern about the potential for the vaccinated to shed Spike Protein to the unvaccinated. See Dr. Piere Kory’s Substack of 20 Feb. CLICK HERE to view. As Dr. Kory points out, “COVID “vaccines” are gene therapy products as defined in the FDA’s…

    Read more

    18 days ago · 64 likes · 9 comments · phillip.altman

    WORLDWIDE CENSORSHIP IS UNDER WAY –

    “Google Isn’t Just Trying to Rewrite History. It’s at the Centre of a Worldwide Web of Censorship”

    https://dailysceptic.org/2024/02/25/google-isnt-just-trying-to-rewrite-history-its-at-the-centre-of-a-worldwide-web-of-censorship/


    TUCKER CARLSON INTERVIEW – JUST 6 MINUTES

    Steve Kirsch Tags the COVID Jab as the ‘Most Dangerous Vaccine of All Time’ The VAERS system has identified 770 safety signals related to the COVID-19 vaccine.

    “That is mind-blowing. That is not a three-alarm fire. That is a 770-alarm fire.” So, what did the CDC do? “They said nothing.”

    https://twitter.com/VigilantFox/status/1761369027685793810

    FOREIGN DNA SHOULD NOT BE IN THE VACCINES – IT CAN ENTER THE DNA IN THE NUCLEUS OF EACH CELL

    Kevin McKernan testifies about how the FDA and Regulators, funded by those who profit from the deception in a great conflict of interest, put the human genome at risk by downplaying the risk of DNA integration.

    Crimes Against Humanity Case Phase 1 Starts At The Same Time We Learn That Covid "Vaccine" DNA Integration Into Ovaries Chromosomes 19 & 12 Is Now Confirmed! Lying Health Ministers, CDC, W.H.O. OH MY!

    This video needs to go viral! SHARE! IoJ is filing an injunction to stop the shots pronto based on the evidence in this Substack article. Our Donation Drive is now open!!! We can win this! Everyone’s going down dammit. This is just unacceptable. The human genome, heritage of humanity is at risk from the WHO and regulators cow towing to Big Pharma’s covi…

    Read more

    13 days ago · 84 likes · 34 comments · Interest of Justice

    MICROPLASTICS – WHAT ARE THEY?

    Humanity United Now - Ana Maria Mihalcea, MD, PhD

    Microplastics - aka Nanotechnological Self Assembly Polymers - Are Everywhere - Poisoning Our Biosphere, Food Supply And Humans

    The use of the word microplastics is once again to normalize the self assembly polymers that have been sprayed via illegal Geoengineering and bioengineering operations to transform our biosphere according to the transhumanist agenda. This is literally killing our planet, killing all life and humanity. This microplastics cover story is to explain why the…

    Read more

    5 months ago · 141 likes · 53 comments · Ana Maria Mihalcea, MD, PhD

    TRICKS AND TREATS FOR A COVID JAB IN NEW ZEALAND

    VIDEO - New Zealand Vax Propaganda & subsequent Sudden Deaths "Get the jab, get the treats" (Oct.16, 2021 Super Saturday Vaxathon)

    VIDEO - New Zealand Vax Propaganda & Sudden Deaths "Get the jab, get the treats" (Source: Coronavirus Plushie) Get the jab, get the treats . . . Incentivizing Kiwis to get jabbed by offering them cash prizes, food, free tickets for the rugby, and other kinds of 'treats', was a big part of the 16 Oct, 2021 'Super Saturday Vaxathon…

    19 days ago · 101 likes · 65 comments · Dr. William Makis MD

    99 million patient records and they concluded that the benefits outweigh the risks!?!? We respectfully disagree.

    A multinational Global Vaccine Data Network (GVDN) cohort study of 99 million vaccinated individuals concludes that the benefits of COVID outweigh the risks. My colleagues and I disagree.

    99 million patient records and they concluded that the benefits outweigh the risks!?!? We respectfully disagree.

    Executive summary A new study of over 99 million vaccinated people has been highly promoted in the press with headlines like “Covid Vaccines Linked To Small Increase In Heart And Brain Disorders, Study Finds—But Risk From Infection Is Far Higher.” I’m going to convince you that this is bullshit…

    Read more

    18 days ago · 525 likes · 334 comments · Steve Kirsch

    “All of the harms from the COVID-19 injectable products were predictable, and preventable”

    There are no 'desired proteins' with regard to the modified spike mRNA

    “All of the harms from the COVID-19 injectable products were predictable, and preventable.” Jessica Rose, PhD A Nature publication by Mulroney et al. entitled N1-methylpseudouridylation of mRNA causes +1 ribosomal frameshifting was published on December 6, 2023. The authors showed that N1-methylpseudouridine affects the fidelity of mRNA translation via ri…

    Read more

    3 months ago · 272 likes · 67 comments · Jessica Rose

    Health Canada Hid Their Concerns About Impurities In COVID-19 Shots From Canadians

    COVID Chronicles

    Health Canada Hid Their Concerns About Impurities In COVID-19 Shots From Canadians

    The Epoch Times, a media outlet that is not state-funded, released an article yesterday that was updated today. Everyone around the world should read it. You can find it here. The journalist, Noé Chartier, did an excellent job writing a well-balanced, objective, and factual account. I do not have much to add…

    Read more

    15 days ago · 370 likes · 104 comments · Dr. Byram W. Bridle

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    https://telegra.ph/CMNnews----Your-Credible-Medical-News-Network----Update-27th-February-2024-03-11
    CMNnews -- Your Credible Medical News Network -- Update 27th February 2024 From Global sources -- Updated Twice Weekly -- CMNNEWS -- We roam the planet for the best Medical News Stories CMNnews THE DOCTORS MONKEY NOT SEE — MONKEY NOT HEAR — MONKEY NOT SPEAK HISTORIC AUSTRALIAN SUPREME COURT DECISION STATE GOVERNMENT FOUND “ACTED UNLAWFULLY” IN REGARD TO VACCINE MANDATES ON POLICE AND AMBULANCE WORKERS Supreme Court bombshell: Queensland’s mandatory Covid vaccine orders ‘unlawful’ Excerpts: Dozens of police and health workers have won a mammoth legal battle over mandatory Covid vaccination orders. Vanda Carson court reporter Courier Mail Newspaper Queensland, Australia 2 min read In a 115-page decision handed down by Justice Glenn Martin on Tuesday he declared police commissioner Katarina Carroll’s direction for mandatory Covid-19 vaccination issued in December 2021 was unlawful under the Human Rights Act and banned her from taking any steps to enforce the direction. He also ruled that a similar order by John Wakefield, the director general of Queensland Health’s equivalent vaccination policy “is of no effect” and Mr Wakefield be blocked from forcing paramedics to have the injection. The workers did not have to be vaccinated while their legal fight was underway. Ms Carroll and Mr Wakefield are also banned from disciplining any of the paramedics and police officers. “I am not satisfied that the (police) Commissioner has demonstrated that she gave proper consideration to the human rights that might have been affected by her decisions,” Justice Martin said in relation to the police staff. “I do not accept that the Commissioner had … considered whether the decision would be compatible with human rights,” he noted in his 115-page decision. “By failing to give proper consideration, the making of each of those decisions was unlawful. “Despite the revocation of the QPS Directions, a finding of unlawfulness is still available.” Link: https://www.couriermail.com.au/truecrimeaustralia/police-courts-qld/supreme-court-bombshell-qlds-mandatory-covid-vaccine-orders-unlawful/news-story/4dcc6ca18dae261249fd7988642192fb Share CMNNews -- The Credible Medical News Network Update Article: Supreme Court bombshell: Qld’s mandatory Covid vaccine orders ‘unlawful’ Excerpts: Dozens of police and health workers including paramedics have won a mammoth legal battle over mandatory ­vaccination orders after the Supreme Court declared they were unlawful. A spokeswoman for the Nurses’ Professional Association of Queensland (NPAQ) said the Supreme Court ruling “ highlighted how Queensland Health has violated thousands of healthcare workers’ rights”. The association highlighted that during a workforce crisis there were members who were stood due to the vaccine mandate who are dying to return to work. “We have nurses and midwives sitting at home during a workforce crisis and the healthcare system’s unlawful decisions are directly to blame,” the spokeswoman said. “NPAQ is currently liaising with our legal team to explore legal avenues for our members in light of today’s Supreme Court outcome.” https://www.couriermail.com.au/truecrimeaustralia/police-courts-qld/supreme-court-bombshell-qlds-mandatory-covid-vaccine-orders-unlawful/news-story/4dcc6ca18dae261249fd7988642192fb COVID-19 vaccine mandates 'unlawful' for emergency services, court finds The court on Tuesday delivered its judgments in three lawsuits brought by 86 parties against Queensland Police Service and Queensland Ambulance Service for their directions to workers issued in 2021 and 2022. The court found Police Commissioner Katarina Carroll failed to give proper consideration to human rights relevant to the decision to issue the vaccine mandate. “The court also found the directions limited the human rights of workers because they were required to undergo a medical procedure without full consent ….” Australian Senate finally acknowledge excess deaths are concerning : Letter from Australian Senator Ralph Babet SENATOR RALPH BABET — IS THIS THE GREATEST SENATE DECISION IN HISTORY? TWO MINUTE VIDEO JIM FERGUSON – “THIS IS GENOCIDE – MURDER OF MILLIONS AND POSSIBLY BILLIONS OF PEOPLE” – “THE PRIME MINISTER COULD BE INVOLVED” -- “THESE ARE CRIMES AGAINST HUMANITY” “Explosive allegations against top Government officials in the UK Government update. As Member of Parliament Andrew Bridgen prepares to present evidence of potential criminal conduct involving Prime Minister Rishi Sunak and his cabinet to London's Metropolitan Police Commissioner Mark Rowley, we explore the mindset of others who might be implicated in alleged widespread wrongdoing, including potential mass genocide and profiteering. Will they now do the right thing and blow the lid on whats really been going on! If the gatekeepers in our Security Services and Police are compromised or complicit in what is arguably the greatest potential crime against humanity of all time then all bets are off as to what happens next.” https://twitter.com/i/status/1761505188056072263 DR DAVID MARTIN EXPLAINS WHO THEY ARE AND HOW THEY ARE DOING THIS TO US “THEY WERE CONVICTED OF ANTI-TRUST CRIMES” “THIS IS A CRIMINAL CONSPIRACY” “WHO IS MOVING THE STICK – WELLCOME, GATES AND ROCKEFELLER” “THIS IS A VIOLATION OF SWISS LAW” Dr. David Martin Reveals Who Is Pulling the Strings Behind the World Health Organization Who are “THEY”? “We have to name the names” in the worst miscarriage of medical science in history. Is it the World Health Organization? Dr. David Martin says Tedros is just a puppet with a “giant stick up his ass, which is what’s making his mouth move… 18 days ago · 446 likes · 136 comments · The Vigilant Fox BILL GATES DONATION TO WORLD HEALTH ORGANIZATION JIM FERGUSON INTERVIEWS ANDREW BRIDGEN -- “Exclusive Breaking News: Evidence to be presented that criminal activity has been committed by the very top of Government in the UK. Rishi Sunak British Prime Minister may face a criminal investigation and face potential criminal charges of the most egregious kind. British MP Andrew Bridgen has written to Mark Rowley Commissioner of the Metropolitan Police and the most senior of Police officers to have a three hour meeting where experts and whistle blowers will lay out the evidence where potential criminal activity has been conducted by the very top of Government and the civil service in the UK Parliament has been deliberately misled over the vaccine contracts. This matter may be taken to Parliamentary standards in addition to the presentation of evidence to the Police and the Security services. "heads of governments around the world and others below them have engaged in what is tantamount to treason against the public" Office of National Statistics (ONS) figures on Excess Deaths are being covered up. "there is a huge coverup going on" In August 2019 a member of the security services stated that there was a pandemic coming and not to take any of the vaccines. Bill gates and Rishi Sunak invested heavily into the Pharma companies like Pfizer and Moderna prior to the pandemic. Did they have insider knowledge about what was being planned in a coming pandemic! 75% of congressmen and woman in the United States have investments in Big Pharma. A Pfizer executive stated that a senator could be bought for $10,000. The journalists are complicit in the cover up. Main Stream Media are bought and paid for. A court case has been launched against the former health secretary Matt Hancock for defamation against Andrew Bridgen and this will take place in the Royal Court of Justice.” https://twitter.com/i/status/1761393940874293335 THESE EVIL PEOPLE ARE COMING AFTER OUR PETS – YOUR DOGS AND CATS – A SECURITY CHIEF WARNED “DO NOT TAKE THE VACCINE” – “THE PRIME MINISTER OF THE UK, RISHI SUNAK, INVESTED HALF A BILLION DOLLARS INTO MODERNA TWO TO THREE YEARS BEFORE COVID OCCURRED” – “HE MUST HAVE HAD PRIOR KNOWLEDGE” https://rumble.com/v4ew676-these-evil-monsters-are-coming-after-our-pets.html JIM FERGUSON ON TWITTER @JimFergusonUK “British PM and #WEF2030Agenda devotee #Sunak invested $500 million of his private funds into Moderna through a company called Thelema Partners in a notorious tax haven in the Caymen Islands. Afterwards he stated in parliament that the vaccine was "safe and effective" while then going on to roll out further permissions for Moderna to set up further vaccine producing interests within the UK. Did he use his position as Prime Minister to make massive personal profits while knowingly or even unknowingly causing harm to the British people and has he broken the National Security Act which states "if you're working in secret for a foreign power to use or abuse your knowledge in a way that causes harm to our citizens you will be a criminal." Former Head of MI6 Sir Alex Younger.” 2024 Is the Last Year of Free Speech and Democracy in the Western World https://www.paulcraigroberts.org/2024/02/19/2024-is-the-last-year-of-free-speech-and-democracy-in-the-western-world/ To Understand The Globalists We Must Understand Their Psychopathic Religion https://alt-market.us/to-understand-the-globalists-we-must-understand-their-psychopathic-religion/ TWO BRAVE AND COURAGEOUS DOCTORS #141 - Dr Charles Hoffe, A Persecuted Ethical Doctor Or Dangerous Misinformation Spreader? FREEDOM - LIBERTY - HAPPINESS SUPPORT DOC MALIK About this conversation - Dr Charles Hoffe is a family doctor who lives and works in British Columbia, Canada. He has worked in general practice and emer… 14 days ago · 34 likes · 5 comments · Doc Malik New Zealand COVID-19 Vaccine Victims Documentary: "Silent No More" (June 2023) VIDEO - New Zealand COVID-19 Vaccine Victims Documentary: "Silent No More" (June 2023) VIDEO - New Zealand COVID-19 Vaccine Victims Documentary: "Silent No More" (June 2023… 14 days ago · 122 likes · 57 comments · Dr. William Makis MD LIST OF LAWYERS NOW AVAILABLE FOR LAWSUITS ON COVID VACCINE INJURY https://deeprootsathome.com/list-of-attorneys-worldwide-now-available-for-lawsuits/ Kaboom! — Renowned Neurologist and Thai Red Cross Emerging Infectious Diseases Health Science Centre Lead Prof. Dr. Thiravat Hemachudha Exposes Vaccine-Linked White Clots on Thailand's Popular TV3 "We've just seen this in the last 2 years... but we didn’t see this before the vaccines. The doctor noticed this between two years to one year ago, in about 50% of the patients," Kaboom! Renowned Neurologist and Thai Red Cross Emerging Infectious Diseases Health Science Centre Lead Prof. Dr. Thiravat Hemachudha Exposes Vaccine-Linked White Clots on Thailand's Popular TV3 It’s taking a long time folks, but the worms are crawling out of the cans, and corrupt institutions and politicians are scrambling to seal them back in! Perhaps due to a significant decrease in mRNA vaccine sales influencing pharmaceutical companies… 18 days ago · 103 likes · 30 comments · Aussie17 mRNA VACCINE SHEDDING OF SPIKE PROTEIN As Dr. Kory points out, “COVID “vaccines” are gene therapy products as defined in the FDA’s 2015 document on Gene Product Shedding Studies and all other gene therapy products on the market list shedding as a risk in their [package] insert (Luxterna, Roctavian, Zolgensma) and shed from 7 days to 6 months.” phillip.altman’s Substack mRNA VACCINE SHEDDING OF SPIKE PROTEIN There has been considerable concern about the potential for the vaccinated to shed Spike Protein to the unvaccinated. See Dr. Piere Kory’s Substack of 20 Feb. CLICK HERE to view. As Dr. Kory points out, “COVID “vaccines” are gene therapy products as defined in the FDA’s… Read more 18 days ago · 64 likes · 9 comments · phillip.altman WORLDWIDE CENSORSHIP IS UNDER WAY – “Google Isn’t Just Trying to Rewrite History. It’s at the Centre of a Worldwide Web of Censorship” https://dailysceptic.org/2024/02/25/google-isnt-just-trying-to-rewrite-history-its-at-the-centre-of-a-worldwide-web-of-censorship/ TUCKER CARLSON INTERVIEW – JUST 6 MINUTES Steve Kirsch Tags the COVID Jab as the ‘Most Dangerous Vaccine of All Time’ The VAERS system has identified 770 safety signals related to the COVID-19 vaccine. “That is mind-blowing. That is not a three-alarm fire. That is a 770-alarm fire.” So, what did the CDC do? “They said nothing.” https://twitter.com/VigilantFox/status/1761369027685793810 FOREIGN DNA SHOULD NOT BE IN THE VACCINES – IT CAN ENTER THE DNA IN THE NUCLEUS OF EACH CELL Kevin McKernan testifies about how the FDA and Regulators, funded by those who profit from the deception in a great conflict of interest, put the human genome at risk by downplaying the risk of DNA integration. Crimes Against Humanity Case Phase 1 Starts At The Same Time We Learn That Covid "Vaccine" DNA Integration Into Ovaries Chromosomes 19 & 12 Is Now Confirmed! Lying Health Ministers, CDC, W.H.O. OH MY! This video needs to go viral! SHARE! IoJ is filing an injunction to stop the shots pronto based on the evidence in this Substack article. Our Donation Drive is now open!!! We can win this! Everyone’s going down dammit. This is just unacceptable. The human genome, heritage of humanity is at risk from the WHO and regulators cow towing to Big Pharma’s covi… Read more 13 days ago · 84 likes · 34 comments · Interest of Justice MICROPLASTICS – WHAT ARE THEY? Humanity United Now - Ana Maria Mihalcea, MD, PhD Microplastics - aka Nanotechnological Self Assembly Polymers - Are Everywhere - Poisoning Our Biosphere, Food Supply And Humans The use of the word microplastics is once again to normalize the self assembly polymers that have been sprayed via illegal Geoengineering and bioengineering operations to transform our biosphere according to the transhumanist agenda. This is literally killing our planet, killing all life and humanity. This microplastics cover story is to explain why the… Read more 5 months ago · 141 likes · 53 comments · Ana Maria Mihalcea, MD, PhD TRICKS AND TREATS FOR A COVID JAB IN NEW ZEALAND VIDEO - New Zealand Vax Propaganda & subsequent Sudden Deaths "Get the jab, get the treats" (Oct.16, 2021 Super Saturday Vaxathon) VIDEO - New Zealand Vax Propaganda & Sudden Deaths "Get the jab, get the treats" (Source: Coronavirus Plushie) Get the jab, get the treats . . . Incentivizing Kiwis to get jabbed by offering them cash prizes, food, free tickets for the rugby, and other kinds of 'treats', was a big part of the 16 Oct, 2021 'Super Saturday Vaxathon… 19 days ago · 101 likes · 65 comments · Dr. William Makis MD 99 million patient records and they concluded that the benefits outweigh the risks!?!? We respectfully disagree. A multinational Global Vaccine Data Network (GVDN) cohort study of 99 million vaccinated individuals concludes that the benefits of COVID outweigh the risks. My colleagues and I disagree. 99 million patient records and they concluded that the benefits outweigh the risks!?!? We respectfully disagree. Executive summary A new study of over 99 million vaccinated people has been highly promoted in the press with headlines like “Covid Vaccines Linked To Small Increase In Heart And Brain Disorders, Study Finds—But Risk From Infection Is Far Higher.” I’m going to convince you that this is bullshit… Read more 18 days ago · 525 likes · 334 comments · Steve Kirsch “All of the harms from the COVID-19 injectable products were predictable, and preventable” There are no 'desired proteins' with regard to the modified spike mRNA “All of the harms from the COVID-19 injectable products were predictable, and preventable.” Jessica Rose, PhD A Nature publication by Mulroney et al. entitled N1-methylpseudouridylation of mRNA causes +1 ribosomal frameshifting was published on December 6, 2023. The authors showed that N1-methylpseudouridine affects the fidelity of mRNA translation via ri… Read more 3 months ago · 272 likes · 67 comments · Jessica Rose Health Canada Hid Their Concerns About Impurities In COVID-19 Shots From Canadians COVID Chronicles Health Canada Hid Their Concerns About Impurities In COVID-19 Shots From Canadians The Epoch Times, a media outlet that is not state-funded, released an article yesterday that was updated today. Everyone around the world should read it. You can find it here. The journalist, Noé Chartier, did an excellent job writing a well-balanced, objective, and factual account. I do not have much to add… Read more 15 days ago · 370 likes · 104 comments · Dr. Byram W. Bridle Subscribe to CMNNews - The Credible Medical News Network News From Around the Globe -- Updated Twice Weekly Disclaimer: All content is presented for educational and/or entertainment purposes only. 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  • BREAKING: Integration of corona vaccine-contaminated DNA into the human cell line genome
    2nd Smartest Guy in the World
    This important article further establishes that the Modified mRNA “vaccines” integrate into the cells. While these contaminated cells do not express the entire spike protein, but, rather, only part of it, the net effect is that the DNA of the “vaccinated” is irrevocably altered.

    Any type of integration into the genome, especially when being assaulted by millions of different random sequences from the “vaccine,” will inevitably cause mutations and other damage to the genome, irrespective if the entire spike protein is expressed, or not.

    This DNA contamination ultimately results in the plethora of slow kill bioweapon adverse events that we are now seeing in surging amounts, not limited to prion diseases, turbo cancers, SADS, and so on and so forth.

    The below is translated from Japanese, and it is a rather technical read, but well worth your time.


    by Mao Arakawa (Okudo Hirokushi)

    The essence of the corona vaccine contaminated DNA problem is the possibility of altering the human genome. To validate this possibility, Dr. Ulrike Kaemmerer conducted an experiment to administer the corona vaccine to MCF7 and OVCAR-3 cancer cell lines. Dr. McKernan, consulted by Dr. Kaemmerer, conducted an experiment to detect contaminated DNA from these cell lines. He reports on his blog the first case of contaminated DNA integration into the cancer cell line genome. (2SG: yesterdays article entitled, UPDATE: Doctors Warn mRNA "Vaccines" Could Spur Epidemic of Prion Brain Diseases addresses this.)

    I was interested, so I attempted to recreate the DNA recombinant event that Dr. McKernan identified. In this article, I will show the results of my analysis.

    Nepetalactone Newsletter

    Vaccine targeted qPCR of Cancer Cell Lines treated with BNT162b2

    Ulrike Kaemmerer has treated MCF7 and OvCar3 cancer cell lines with various vaccines. Once transfected they performed cell passaging on these transfected cell lines to dilute out the residual vaccine and identify cells which were transfected. They performed Immunohistochemistry (IHC) on these cells and documented spike expression levels…

    Read more

    14 days ago · 109 likes · 22 comments · Anandamide

    image
    Figure 1
    Dr. Kaemmerer administered the corona vaccine from Pfizer and AstraZeneca to the ovarian tumor cell line OVCAR-3 and, after subculture, confirmed the expression of the spikutanpak by immunohistochemical staining. Deep Sequencing comes at a high cost; therefore, preliminary experiments are required in advance to perform DNA detection experiments. Dr. McKernan first screened post-vaccination cells with qPCR and targeted qPCR-positive cells for deep sequencing.

    Contaminated DNA that is not integrated into the genome is diluted with subculture. In fact, the Ct value of the vector was Ct 30.28 in the first generation, but it was 34.72 in the second generation. The difference in 4Ct is 16 times the difference, and that is the lower concentration in the second passage. Dr. McKernan extracted DNA from two cells subcultured and performed deep sequencing. Sequence data detected SV40, replication origin and spiked DNA. Spike DNA was detected in the full genomic shotgun library of vaccine-treated samples with 3000x coverage. (Coverage means the percentage of the total base pair or locus of the genome covered by sequencing.) Since the coverage in the human genome was 30 times, we can see that the DNA with a large number of copies of the genome was invading the cell.

    As a result, strangely, SNP (monobasic polymorphism) was detected in deep sequencing at the origin of the vaccine plasmid replication (F1 and SV40). This SNP does not exist in the vaccine. In other words, it seems that plasmids are mutating in cells. Also, the coverage of deep sequencing in the replication origin area is higher than average, and the number of copies observed is relatively high, which means that the DNA embedded in the cell may be duplicated and mutated. I mean. Originally, plasmids and SV40 DNA replication require specific enzymes not owned by human cells. Experiments such as the introduction of large amounts of microDNA fragments containing replication points into cells are not usually performed in molecular genetics. It is possible that unexpected DNA replication is occurring within the cell.

    A total of two genomic integrations were observed in the vaccinated cell line from the analysis of Deep Sequencing by Dr. McKernan. Individual arrays of deep sequencing are called 「 leads 」. It was very interesting data, so I tried to re-parse the lead myself.

    image
    Figure 2
    Figure 2 is a lead showing genomic integration in Dr. McKernan's Deep Sequencing Analysis. The subject of the analysis is Genome Integration Leads 1 and 2. You can also read a lot of information from short array data. This time in comparison with the human genomeblat searchTo find homologyblast searchI used it.

    Now, after that, it will be my own re-parse.

    image
    Figure 3
    The top of the array in Figure 3 is the lead. As you can tell by aligning this lead with the 12th chromosome (black) and the spike gene (red) of the Pfizer Corona vaccine, the 12th chromosome (black) is on the way to the spike gene (red). I am switching. And there is a short identical array (here GAGAG) in the place of switching. You can see that the end-recombination (MMEJ, Microhomology-mediated end joining) mediated by microhomology (microhomology) recombinates the contaminated DNA and human genome. Since MMEJ involves multiple intracellular DNA repair enzymes, this recombination is an artifact (mistake product) in the test tube. Instead, gene recombination may have occurred in cells.

    Genome integration occurs on the long arm of chromosome 12, and the FAIM2 gene is present at this locus. FAIM2 is a gene that has been suggested to be associated with cancer malignancy. Recombinations occur on introns (arrays that do not encode proteins), but I do not know how such mutations also affect gene expression.

    image
    Figure 4
    Another example of genomic integration is Figure 4. If you align this lead with chromosome 9 (black) and spike gene (red), you can see that in the lead, chromosome 9 (black) is switching to the spike gene (red) on the way. There is a short identical array (here TCTGCCCT) in the place where this example also switches. After all, it is believed that the contaminated DNA and the human genome were recombined using microhomology. Since there are multiple pathways for DNA repair, which repair pathway is used when foreign DNA is taken into the genome is case-by-case.

    Part of the lead had an Illumina adapter array left. Adapter arrays are arrays granted to PCR amplify and sequence DNA for deep sequencing. Originally, the adapter array is removed during parsing, but often the removal is inadequate and remains in the lead.

    Integration of contaminated DNA into the genome is occurring near Centromea. Let's talk a little about Centromea. Two chromosomes with the same genetic information that can be done after DNA replication are chromatids (sister chromatids). The chromatids are connected until the chromosomes are distributed during cell division, but the region on the connected DNA is Centromea. As such, Centromea is an important area for chromosome separation and distribution.

    image
    Figure 5
    Figure 5 is about the DNA fragments of the spike gene integrated into the genome. On the Pfizer Corona vaccine spike gene, the sequence found in the genome integrated lead was written in red. Due to lead length limitations, the actual integrated array will be even larger. The integrated sequence is part of the spike gene, and it is not possible to make a full-length spike sequence. However, it is unpredictable how contaminated DNA will be inserted into any area of the genome and have any effect.

    image
    Figure 6
    Nucleotype (cario type) means the size, shape, and number of chromosomes. Human chromosomes consist of a total of 46 22 pairs of autosomal and one pair of sex chromosomes. The autosomal is assigned the number 1 chromosome, number 2 chromosome,, number 22 chromosome and number in order of size. The integrated site of contaminated DNA is the FAIM2 locus on the long arm of chromosome 9 and near Centromea on chromosome 12.

    The genomic integration observed this time is the first two cases in cultured cell experiments, but the specific identification of recombinant sequences with the human genome of contaminated DNA is a major advance. Further verification experiments will be advanced in the future. Genome integration, as in Figure 6, does not know which locus actually occurs on the genome. This is exactly the 「 shotgun attack on the genome 」. What happens in cultured cells can also occur in normal cells, with a wide variety of alterations depending on the site of genomic integration. The first predicted catabolism is cancer induction and malignancy. And then, the ones that manifest themselves over time are various genetic diseases.

    What is known as a factor that causes genomic damage is, for example, radiation exposure, but genomic modification by contaminated DNA is different in that it is due to fragments of artificially created genes, and random mutations which are akin to radiation. But it is fundamentally different in nature. This experiment in cultured cells epitomizes genomic integration of contaminated DNA. This is a real problem that a large number of humans around the world, under the name of vaccination, are now experiencing a「 transfection human body experiment 」of contaminated DNA.

    The genomic modification of humanity is a direct consequence of the largest experiment in history of mRNA drug substance harm, and in the future it may be etched in history as the「 original sin 」of humanity.


    Original Social Engineering Sin

    Original Social Engineering Sin
    “...the socio-psychological foundations of socialism is identical to that of the foundations of a state, if there were no institution enforcing socialistic ideas of property, there would be no room for a state, as a state is nothing else than an institution built on taxation and unsolicited, noncontractual interference with the use that private people c…

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    BREAKING: Integration of corona vaccine-contaminated DNA into the human cell line genome 🧬




    https://www.2ndsmartestguyintheworld.com/p/breaking-integration-of-corona-vaccine

    https://telegra.ph/BREAKING-Integration-of-corona-vaccine-contaminated-DNA-into-the-human-cell-line-genome-03-11
    BREAKING: Integration of corona vaccine-contaminated DNA into the human cell line genome 2nd Smartest Guy in the World This important article further establishes that the Modified mRNA “vaccines” integrate into the cells. While these contaminated cells do not express the entire spike protein, but, rather, only part of it, the net effect is that the DNA of the “vaccinated” is irrevocably altered. Any type of integration into the genome, especially when being assaulted by millions of different random sequences from the “vaccine,” will inevitably cause mutations and other damage to the genome, irrespective if the entire spike protein is expressed, or not. This DNA contamination ultimately results in the plethora of slow kill bioweapon adverse events that we are now seeing in surging amounts, not limited to prion diseases, turbo cancers, SADS, and so on and so forth. The below is translated from Japanese, and it is a rather technical read, but well worth your time. by Mao Arakawa (Okudo Hirokushi) The essence of the corona vaccine contaminated DNA problem is the possibility of altering the human genome. To validate this possibility, Dr. Ulrike Kaemmerer conducted an experiment to administer the corona vaccine to MCF7 and OVCAR-3 cancer cell lines. Dr. McKernan, consulted by Dr. Kaemmerer, conducted an experiment to detect contaminated DNA from these cell lines. He reports on his blog the first case of contaminated DNA integration into the cancer cell line genome. (2SG: yesterdays article entitled, UPDATE: Doctors Warn mRNA "Vaccines" Could Spur Epidemic of Prion Brain Diseases addresses this.) I was interested, so I attempted to recreate the DNA recombinant event that Dr. McKernan identified. In this article, I will show the results of my analysis. Nepetalactone Newsletter Vaccine targeted qPCR of Cancer Cell Lines treated with BNT162b2 Ulrike Kaemmerer has treated MCF7 and OvCar3 cancer cell lines with various vaccines. Once transfected they performed cell passaging on these transfected cell lines to dilute out the residual vaccine and identify cells which were transfected. They performed Immunohistochemistry (IHC) on these cells and documented spike expression levels… Read more 14 days ago · 109 likes · 22 comments · Anandamide image Figure 1 Dr. Kaemmerer administered the corona vaccine from Pfizer and AstraZeneca to the ovarian tumor cell line OVCAR-3 and, after subculture, confirmed the expression of the spikutanpak by immunohistochemical staining. Deep Sequencing comes at a high cost; therefore, preliminary experiments are required in advance to perform DNA detection experiments. Dr. McKernan first screened post-vaccination cells with qPCR and targeted qPCR-positive cells for deep sequencing. Contaminated DNA that is not integrated into the genome is diluted with subculture. In fact, the Ct value of the vector was Ct 30.28 in the first generation, but it was 34.72 in the second generation. The difference in 4Ct is 16 times the difference, and that is the lower concentration in the second passage. Dr. McKernan extracted DNA from two cells subcultured and performed deep sequencing. Sequence data detected SV40, replication origin and spiked DNA. Spike DNA was detected in the full genomic shotgun library of vaccine-treated samples with 3000x coverage. (Coverage means the percentage of the total base pair or locus of the genome covered by sequencing.) Since the coverage in the human genome was 30 times, we can see that the DNA with a large number of copies of the genome was invading the cell. As a result, strangely, SNP (monobasic polymorphism) was detected in deep sequencing at the origin of the vaccine plasmid replication (F1 and SV40). This SNP does not exist in the vaccine. In other words, it seems that plasmids are mutating in cells. Also, the coverage of deep sequencing in the replication origin area is higher than average, and the number of copies observed is relatively high, which means that the DNA embedded in the cell may be duplicated and mutated. I mean. Originally, plasmids and SV40 DNA replication require specific enzymes not owned by human cells. Experiments such as the introduction of large amounts of microDNA fragments containing replication points into cells are not usually performed in molecular genetics. It is possible that unexpected DNA replication is occurring within the cell. A total of two genomic integrations were observed in the vaccinated cell line from the analysis of Deep Sequencing by Dr. McKernan. Individual arrays of deep sequencing are called 「 leads 」. It was very interesting data, so I tried to re-parse the lead myself. image Figure 2 Figure 2 is a lead showing genomic integration in Dr. McKernan's Deep Sequencing Analysis. The subject of the analysis is Genome Integration Leads 1 and 2. You can also read a lot of information from short array data. This time in comparison with the human genomeblat searchTo find homologyblast searchI used it. Now, after that, it will be my own re-parse. image Figure 3 The top of the array in Figure 3 is the lead. As you can tell by aligning this lead with the 12th chromosome (black) and the spike gene (red) of the Pfizer Corona vaccine, the 12th chromosome (black) is on the way to the spike gene (red). I am switching. And there is a short identical array (here GAGAG) in the place of switching. You can see that the end-recombination (MMEJ, Microhomology-mediated end joining) mediated by microhomology (microhomology) recombinates the contaminated DNA and human genome. Since MMEJ involves multiple intracellular DNA repair enzymes, this recombination is an artifact (mistake product) in the test tube. Instead, gene recombination may have occurred in cells. Genome integration occurs on the long arm of chromosome 12, and the FAIM2 gene is present at this locus. FAIM2 is a gene that has been suggested to be associated with cancer malignancy. Recombinations occur on introns (arrays that do not encode proteins), but I do not know how such mutations also affect gene expression. image Figure 4 Another example of genomic integration is Figure 4. If you align this lead with chromosome 9 (black) and spike gene (red), you can see that in the lead, chromosome 9 (black) is switching to the spike gene (red) on the way. There is a short identical array (here TCTGCCCT) in the place where this example also switches. After all, it is believed that the contaminated DNA and the human genome were recombined using microhomology. Since there are multiple pathways for DNA repair, which repair pathway is used when foreign DNA is taken into the genome is case-by-case. Part of the lead had an Illumina adapter array left. Adapter arrays are arrays granted to PCR amplify and sequence DNA for deep sequencing. Originally, the adapter array is removed during parsing, but often the removal is inadequate and remains in the lead. Integration of contaminated DNA into the genome is occurring near Centromea. Let's talk a little about Centromea. Two chromosomes with the same genetic information that can be done after DNA replication are chromatids (sister chromatids). The chromatids are connected until the chromosomes are distributed during cell division, but the region on the connected DNA is Centromea. As such, Centromea is an important area for chromosome separation and distribution. image Figure 5 Figure 5 is about the DNA fragments of the spike gene integrated into the genome. On the Pfizer Corona vaccine spike gene, the sequence found in the genome integrated lead was written in red. Due to lead length limitations, the actual integrated array will be even larger. The integrated sequence is part of the spike gene, and it is not possible to make a full-length spike sequence. However, it is unpredictable how contaminated DNA will be inserted into any area of the genome and have any effect. image Figure 6 Nucleotype (cario type) means the size, shape, and number of chromosomes. Human chromosomes consist of a total of 46 22 pairs of autosomal and one pair of sex chromosomes. The autosomal is assigned the number 1 chromosome, number 2 chromosome,, number 22 chromosome and number in order of size. The integrated site of contaminated DNA is the FAIM2 locus on the long arm of chromosome 9 and near Centromea on chromosome 12. The genomic integration observed this time is the first two cases in cultured cell experiments, but the specific identification of recombinant sequences with the human genome of contaminated DNA is a major advance. Further verification experiments will be advanced in the future. Genome integration, as in Figure 6, does not know which locus actually occurs on the genome. This is exactly the 「 shotgun attack on the genome 」. What happens in cultured cells can also occur in normal cells, with a wide variety of alterations depending on the site of genomic integration. The first predicted catabolism is cancer induction and malignancy. And then, the ones that manifest themselves over time are various genetic diseases. What is known as a factor that causes genomic damage is, for example, radiation exposure, but genomic modification by contaminated DNA is different in that it is due to fragments of artificially created genes, and random mutations which are akin to radiation. But it is fundamentally different in nature. This experiment in cultured cells epitomizes genomic integration of contaminated DNA. This is a real problem that a large number of humans around the world, under the name of vaccination, are now experiencing a「 transfection human body experiment 」of contaminated DNA. The genomic modification of humanity is a direct consequence of the largest experiment in history of mRNA drug substance harm, and in the future it may be etched in history as the「 original sin 」of humanity. Original Social Engineering Sin Original Social Engineering Sin “...the socio-psychological foundations of socialism is identical to that of the foundations of a state, if there were no institution enforcing socialistic ideas of property, there would be no room for a state, as a state is nothing else than an institution built on taxation and unsolicited, noncontractual interference with the use that private people c… Read full story They want you dead. Do NOT comply. Upgrade to paid Shop 2SG merch Use code 2SGPET for 10% off PetMectin Use code 2SGPET for 10% off PetDazole Use code 2SGPET for 10% off FishCycline BREAKING: Integration of corona vaccine-contaminated DNA into the human cell line genome 🧬 https://www.2ndsmartestguyintheworld.com/p/breaking-integration-of-corona-vaccine https://telegra.ph/BREAKING-Integration-of-corona-vaccine-contaminated-DNA-into-the-human-cell-line-genome-03-11
    WWW.2NDSMARTESTGUYINTHEWORLD.COM
    BREAKING: Integration of corona vaccine-contaminated DNA into the human cell line genome
    This important article further establishes that the Modified mRNA “vaccines” integrate into the cells. While these contaminated cells do not express the entire spike protein, but, rather, only part of it, the net effect is that the DNA of the “vaccinated” is irrevocably altered.
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  • Luciferase Microarray Patches Contain DARPA Hydrogel & Autonomous Insect Cyborg Sentinels
    June 21, 2023 by Dr. Ariyana Love
    By Dr. Ariyana Love

    Queensland’s first needle-free “vaccine” facility just opened in Australia, yesterday. The microarray patch for intradermal delivery technology is also being called a Nanopatch and it’s aimed at our children.

    3D printed microarray patches (MAP’s) are comprised of a series of micrometer-sized projections that can painlessly puncture the skin and access the epidermal/dermal layer, delivering drugs and chemicals into the interstitial fluids of the human body. It also allows for external control of delayed release of drugs and repeated dosage over time. This technology was already being developed back in the 1970’s.

    In May of 2023, Micron Biomedical announced Phase 1/2 data from the first-ever clinical trial of a “vaccine” patch in children – including infants as young as nine months old. This study was tested on Gambian children.

    In October of 2022, the first official Luciferase patch trial on children using a placebo, began in Brisbane, Australia. The trial was led by Vaxxas. A number of phase-one clinical trials in adults were already conducted by Vaxxas according to Project Manager, Ben Baker.

    Vaxxas, founded by UQ commercialization company UniQuest in 2011, received $A30 million (US$22 million) through the Biomedical Advanced Research and Development Authority (BARDA) to support “pandemic” deployment of their high-density micro-array patch (HD-MAP). Vaxxas is partnered with the U.S. Government and funded by Bill and Melinda Gates. The microarray patch is supposedly intended to inoculate children from middle to low income countries with measles, rubella, and polio.

    This microarray patch technology is scheduled to be mandated for children worldwide and it’s on the national immunization schedule for children in Australia. UNICEF is driving the research, development and scale of microarray patches for children. They’re keen on “identifying barriers for scaling and investigating the need for market pull incentives to spark interest and endorsement by vaccine manufacturers.” And of course the World Harm Organization (WHO) is involved with pushing the measles-rubella microarray patch on children.

    DNA from human origin

    The antibody used in the microarray (MA) patches comes from human origin, according to scientific literature (See paragraph #4 and 2.2. Antibody Stability Study). The patches use “nonspecific human Ig” and the “human hlg” which is a human leukocyte antigen, as well as other “nonspecific” amounts of human DNA plasma, including human lgG1 and human lgG2. It is well known that injecting human DNA into humans induces inflammation, autoimmunity and rapid cancer growth.

    The core–shell MA patch has two delayed burst releases at days 10 and 21. Included in the patches is the use of “nondegradable poly(ethylene-co-vinyl acetate) (EVA, for the sustained release of human DNA), hyaluronic acid scaffolds, glycol chitosan, and oxidized alginate hydrogels.” (See paragraph two).

    Glycol chitosan is insect DNA which is highly toxic to humans. It has never been approved by the FDA for use in humans. Hyaluronic acid based scaffolds is used for tissue engineering and so is synthetic mRNA.

    Johnson and Johnson developed the Luciferase microarray patch (See paragraph entitled, 2.3. Vector) containing the Adenovirus 5 vector for targeted deletion of the E1 and E3 genes, located on the X-chromosome.

    PLEASE READ: EPIGENETICS: Vaccines Are Deleting Human Genes & Transfecting Cells With Ebola/Marburg

    This scientific paper reveals that Luciferase hydrogel is chimeric DNA from cross species genomic splicing. The Luciferase patches are being marketed (See bottom of page) as something that will “reduce the rate of HIV infections”. Incidentally, governments are coercing schools to mandate HIV testing of children.

    DARPA hydrogel

    The Defense Advanced Research Projects Agency (DARPA) is a research and development agency of the United States Department of Defense responsible for the development of emerging technologies for use by the military.

    DARPA’s hydrogel replicates into rectangular crystal structures within minutes after coming into contact with body fluids. It grows a crystalline sheath above your muscle and beneath your skin which is magnetic. It acts as an antennae inside the human body that can transmit your internal data through the Internet and receive commands from towers as it replicates and expands throughout the entire body.

    Whole parasite “vaccines”

    Also contained within some embodiment’s of the DARPA hydrogel patches are Sentinels. Under a highly classified program DARPA has been weaponizing insects for decades such as GMO mosquitos that carry GMO parasite eggs coded with synthetic mRNA. These parasite eggs are otherwise known as “whole parasite vaccines“.

    PLEASE READ: Malaria Parasites In “Vaccines” Target Placenta, Kill Babies In Utero

    This peer-reviewed paper discusses “Cyropreserved Whole-Parasite Vaccines” using the deadly P. falciparum Malaria parasite to target in particular, the CD4+ T cells and destroy them by inducing cell death. Please also read here, here and here.

    The Sentinels

    Sentinels are also found within the DARPA hydrogel Luciferase microarray patches.

    DARPA has a full Hybrid Insect MEMS program called “Sentinel”. The D.O.D. is also in on this. Much of the funding for this project comes from DARPA’s Microsystems Technology Office (MTO), which has devoted more than US$2 million to the Hybrid Insect MEMS (HI-MEMS) program.

    Micro-Electro-Mechanical Systems (MEMS), otherwise known as micromachined devices uses organic insects that have been morphed into externally controllable electromechanical devices and ‘living’ biosensors, using genetically modified microorganisms. Micro-mechanical systems are placed inside the insects during the early stages of metamorphosis, allowing for tissue-machine interface and control over insect locomotion. Insect cyborgs have most of the machine component inside the insect body providing stealthy robots that use muscle actuators. Motion trajectories are obtained either from GPS coordinates, or using RF, optical, ultrasonic signals based remote control. The Sentinels work as microsensors and they also can modulate light beams. Through heterogeneous integration, they have merged the Sentinels into a circuitry nanotech system.

    While this is a highly classified and secretive project, there’s a paper trail. In 2018, the U.S. Government awarded DARPA a research and development contract funding DARPA’s SENTINEL # HR001118S0005 project to the tune of 10 million dollars. The first Sentinel patent was registered by GeneNews, in 2010. The second Sentinel patent # 7,662,558, entitled “Method of profiling gene expression in a human subject” was registered in 2018.

    But who could anticipate that Sentinels would be used inside the human body? Since 2009, Sentinels have been used internally for a breast cancer excision. They can slice right through tumors which explains why my clients are being internally lacerated by these Sentinels, inflicting terrible pain and causing red skin lesions to appear. Also according to client testimonials and peer-reviewed literature, Sentinels shoot out electromagnetic beams and attempt to influence your nervous system using electricity. They borrow into the nervous system and can “read thoughts,” anticipate your movements and attempt to control their host.

    The hydrogel-based encapsulation (nanotech) system for genetically modified organisms (GMMs) incorporates a biocompatible multilayer tough shell and an alginate-based core. Sentinels are the core controller of the Operating System. They regulate cell to cell communication between the AI parasites, organoids, hydras, worms and poisonous anaerobic bacteria in vivo, as the linked document shows.

    “Microelectronic integrated circuits can be thought of as the “brains” of a system and MEMS augments this decision-making capability with “eyes” and “arms”, to allow microsystems to sense and control the environment. Sensors gather information from the environment through measuring mechanical, thermal, biological, chemical, optical, and magnetic phenomena. The electronics then process the information derived from the sensors and through some decision making capability direct the actuators to respond by moving, positioning, regulating, pumping, and filtering, thereby controlling the environment for some desired outcome or purpose. Furthermore, because MEMS devices are manufactured using batch fabrication techniques, similar to ICs, unprecedented levels of functionality, reliability, and sophistication can be placed on a small silicon chip at a relatively low cost.”

    DARPA openly admits to using AI for brain computer interface with humans through it’s Explainable Artificial Intelligence (XAI) program. Sentinels are contained within a small silicon chip that looks very similar to the chips Dr. Pablo Campra found in the Covid-19 vials.

    In 2017, Finland developed nanocellulose-alginate hydrogel suitable for 3D printing.

    Implantable hydrogel biosensors are scheduled to be used in Covid-19 inoculations and microarray patches. Hillman Laboratories partnered with John Hopkins University, admit that they want to “take the microarray patches door to door“.

    One of my clients was a victim of a U.S. government pilot project in Seattle Washington. GMO mosquitos are being unleashed in Florida and other states as well. My client, her daughter and best friend were congregated at a church function outdoors when they were “beaten by mosquito’s,” as she put it. These mosquito’s were smaller than the typical mosquitos they have in Washington state and they had unusual markings. They could not feel the bites but saw the mosquito’s biting. Later, people from the congregation broke out in welts where they were bitten and had terrible pains all over their bodies. Now my client and her daughter are riddled with Sentinels which crawl everywhere in their bodies and torture them. These Sentinels belong to DARPA’s weaponized insects project. My clients best friend could not endure and she died before they discovered my protocols. I have several other clients whom are being tortured by Sentinels and my protocols are helping them. Other clients have already detoxed the Sentinel and DARPA hydrogel out of their bodies.

    ALSO READ: “YIKES! Hydrogel Nano-biotechnology in Vaccines and Nasal Swab Tests Capable of Electronically Linking Human Brains to Cloud Wirelessly” by State of The Nation.

    Please consider donating to Dr. Ariyana Love’s investigative research and ministry, here.

    If you require a health consultation please schedule with Dr. Love, here.

    Contact Dr. Love at [email protected] or call her cell at +1 928-892-8736.

    Follow Dr. Love on Telegram @DrAriyanaLove and on Twitter @drloveariyana.

    https://ambassadorlove.blog/2023/06/21/luciferase-microarray-patches-contain-darpa-hydrogel-autonomous-insect-cyborg-sentinels/
    Luciferase Microarray Patches Contain DARPA Hydrogel & Autonomous Insect Cyborg Sentinels June 21, 2023 by Dr. Ariyana Love By Dr. Ariyana Love Queensland’s first needle-free “vaccine” facility just opened in Australia, yesterday. The microarray patch for intradermal delivery technology is also being called a Nanopatch and it’s aimed at our children. 3D printed microarray patches (MAP’s) are comprised of a series of micrometer-sized projections that can painlessly puncture the skin and access the epidermal/dermal layer, delivering drugs and chemicals into the interstitial fluids of the human body. It also allows for external control of delayed release of drugs and repeated dosage over time. This technology was already being developed back in the 1970’s. In May of 2023, Micron Biomedical announced Phase 1/2 data from the first-ever clinical trial of a “vaccine” patch in children – including infants as young as nine months old. This study was tested on Gambian children. In October of 2022, the first official Luciferase patch trial on children using a placebo, began in Brisbane, Australia. The trial was led by Vaxxas. A number of phase-one clinical trials in adults were already conducted by Vaxxas according to Project Manager, Ben Baker. Vaxxas, founded by UQ commercialization company UniQuest in 2011, received $A30 million (US$22 million) through the Biomedical Advanced Research and Development Authority (BARDA) to support “pandemic” deployment of their high-density micro-array patch (HD-MAP). Vaxxas is partnered with the U.S. Government and funded by Bill and Melinda Gates. The microarray patch is supposedly intended to inoculate children from middle to low income countries with measles, rubella, and polio. This microarray patch technology is scheduled to be mandated for children worldwide and it’s on the national immunization schedule for children in Australia. UNICEF is driving the research, development and scale of microarray patches for children. They’re keen on “identifying barriers for scaling and investigating the need for market pull incentives to spark interest and endorsement by vaccine manufacturers.” And of course the World Harm Organization (WHO) is involved with pushing the measles-rubella microarray patch on children. DNA from human origin The antibody used in the microarray (MA) patches comes from human origin, according to scientific literature (See paragraph #4 and 2.2. Antibody Stability Study). The patches use “nonspecific human Ig” and the “human hlg” which is a human leukocyte antigen, as well as other “nonspecific” amounts of human DNA plasma, including human lgG1 and human lgG2. It is well known that injecting human DNA into humans induces inflammation, autoimmunity and rapid cancer growth. The core–shell MA patch has two delayed burst releases at days 10 and 21. Included in the patches is the use of “nondegradable poly(ethylene-co-vinyl acetate) (EVA, for the sustained release of human DNA), hyaluronic acid scaffolds, glycol chitosan, and oxidized alginate hydrogels.” (See paragraph two). Glycol chitosan is insect DNA which is highly toxic to humans. It has never been approved by the FDA for use in humans. Hyaluronic acid based scaffolds is used for tissue engineering and so is synthetic mRNA. Johnson and Johnson developed the Luciferase microarray patch (See paragraph entitled, 2.3. Vector) containing the Adenovirus 5 vector for targeted deletion of the E1 and E3 genes, located on the X-chromosome. PLEASE READ: EPIGENETICS: Vaccines Are Deleting Human Genes & Transfecting Cells With Ebola/Marburg This scientific paper reveals that Luciferase hydrogel is chimeric DNA from cross species genomic splicing. The Luciferase patches are being marketed (See bottom of page) as something that will “reduce the rate of HIV infections”. Incidentally, governments are coercing schools to mandate HIV testing of children. DARPA hydrogel The Defense Advanced Research Projects Agency (DARPA) is a research and development agency of the United States Department of Defense responsible for the development of emerging technologies for use by the military. DARPA’s hydrogel replicates into rectangular crystal structures within minutes after coming into contact with body fluids. It grows a crystalline sheath above your muscle and beneath your skin which is magnetic. It acts as an antennae inside the human body that can transmit your internal data through the Internet and receive commands from towers as it replicates and expands throughout the entire body. Whole parasite “vaccines” Also contained within some embodiment’s of the DARPA hydrogel patches are Sentinels. Under a highly classified program DARPA has been weaponizing insects for decades such as GMO mosquitos that carry GMO parasite eggs coded with synthetic mRNA. These parasite eggs are otherwise known as “whole parasite vaccines“. PLEASE READ: Malaria Parasites In “Vaccines” Target Placenta, Kill Babies In Utero This peer-reviewed paper discusses “Cyropreserved Whole-Parasite Vaccines” using the deadly P. falciparum Malaria parasite to target in particular, the CD4+ T cells and destroy them by inducing cell death. Please also read here, here and here. The Sentinels Sentinels are also found within the DARPA hydrogel Luciferase microarray patches. DARPA has a full Hybrid Insect MEMS program called “Sentinel”. The D.O.D. is also in on this. Much of the funding for this project comes from DARPA’s Microsystems Technology Office (MTO), which has devoted more than US$2 million to the Hybrid Insect MEMS (HI-MEMS) program. Micro-Electro-Mechanical Systems (MEMS), otherwise known as micromachined devices uses organic insects that have been morphed into externally controllable electromechanical devices and ‘living’ biosensors, using genetically modified microorganisms. Micro-mechanical systems are placed inside the insects during the early stages of metamorphosis, allowing for tissue-machine interface and control over insect locomotion. Insect cyborgs have most of the machine component inside the insect body providing stealthy robots that use muscle actuators. Motion trajectories are obtained either from GPS coordinates, or using RF, optical, ultrasonic signals based remote control. The Sentinels work as microsensors and they also can modulate light beams. Through heterogeneous integration, they have merged the Sentinels into a circuitry nanotech system. While this is a highly classified and secretive project, there’s a paper trail. In 2018, the U.S. Government awarded DARPA a research and development contract funding DARPA’s SENTINEL # HR001118S0005 project to the tune of 10 million dollars. The first Sentinel patent was registered by GeneNews, in 2010. The second Sentinel patent # 7,662,558, entitled “Method of profiling gene expression in a human subject” was registered in 2018. But who could anticipate that Sentinels would be used inside the human body? Since 2009, Sentinels have been used internally for a breast cancer excision. They can slice right through tumors which explains why my clients are being internally lacerated by these Sentinels, inflicting terrible pain and causing red skin lesions to appear. Also according to client testimonials and peer-reviewed literature, Sentinels shoot out electromagnetic beams and attempt to influence your nervous system using electricity. They borrow into the nervous system and can “read thoughts,” anticipate your movements and attempt to control their host. The hydrogel-based encapsulation (nanotech) system for genetically modified organisms (GMMs) incorporates a biocompatible multilayer tough shell and an alginate-based core. Sentinels are the core controller of the Operating System. They regulate cell to cell communication between the AI parasites, organoids, hydras, worms and poisonous anaerobic bacteria in vivo, as the linked document shows. “Microelectronic integrated circuits can be thought of as the “brains” of a system and MEMS augments this decision-making capability with “eyes” and “arms”, to allow microsystems to sense and control the environment. Sensors gather information from the environment through measuring mechanical, thermal, biological, chemical, optical, and magnetic phenomena. The electronics then process the information derived from the sensors and through some decision making capability direct the actuators to respond by moving, positioning, regulating, pumping, and filtering, thereby controlling the environment for some desired outcome or purpose. Furthermore, because MEMS devices are manufactured using batch fabrication techniques, similar to ICs, unprecedented levels of functionality, reliability, and sophistication can be placed on a small silicon chip at a relatively low cost.” DARPA openly admits to using AI for brain computer interface with humans through it’s Explainable Artificial Intelligence (XAI) program. Sentinels are contained within a small silicon chip that looks very similar to the chips Dr. Pablo Campra found in the Covid-19 vials. In 2017, Finland developed nanocellulose-alginate hydrogel suitable for 3D printing. Implantable hydrogel biosensors are scheduled to be used in Covid-19 inoculations and microarray patches. Hillman Laboratories partnered with John Hopkins University, admit that they want to “take the microarray patches door to door“. One of my clients was a victim of a U.S. government pilot project in Seattle Washington. GMO mosquitos are being unleashed in Florida and other states as well. My client, her daughter and best friend were congregated at a church function outdoors when they were “beaten by mosquito’s,” as she put it. These mosquito’s were smaller than the typical mosquitos they have in Washington state and they had unusual markings. They could not feel the bites but saw the mosquito’s biting. Later, people from the congregation broke out in welts where they were bitten and had terrible pains all over their bodies. Now my client and her daughter are riddled with Sentinels which crawl everywhere in their bodies and torture them. These Sentinels belong to DARPA’s weaponized insects project. My clients best friend could not endure and she died before they discovered my protocols. I have several other clients whom are being tortured by Sentinels and my protocols are helping them. Other clients have already detoxed the Sentinel and DARPA hydrogel out of their bodies. ALSO READ: “YIKES! Hydrogel Nano-biotechnology in Vaccines and Nasal Swab Tests Capable of Electronically Linking Human Brains to Cloud Wirelessly” by State of The Nation. Please consider donating to Dr. Ariyana Love’s investigative research and ministry, here. If you require a health consultation please schedule with Dr. Love, here. Contact Dr. Love at [email protected] or call her cell at +1 928-892-8736. Follow Dr. Love on Telegram @DrAriyanaLove and on Twitter @drloveariyana. https://ambassadorlove.blog/2023/06/21/luciferase-microarray-patches-contain-darpa-hydrogel-autonomous-insect-cyborg-sentinels/
    AMBASSADORLOVE.BLOG
    Luciferase Microarray Patches Contain DARPA Hydrogel & Autonomous Insect Cyborg Sentinels
    By Dr. Ariyana Love Queensland’s first needle-free “vaccine” facility just opened in Australia, yesterday. The microarray patch for intradermal delivery technology is also being c…
    0 Comments 0 Shares 17601 Views
  • Prof Didier Raoult, French physician and microbiologist specialising in infectious diseases, and one of the Top Scientists in the world with a H-Index of 212, on France's CNEWS:

    -------------------------
    What Pfizer said was that there was only manipulated RNA, ...and that there was no DNA.

    However, there is a considerable amount of DNA in these vaccines. And we have measured it too. The quantity is huge.

    That is to say, what was supposed to be purified, the RNA was produced by bacteria in which a mini-chromosome had been inserted and it was necessary to purify this mini-chromosome and remove the DNA that had been used to make the RNA. This was not done.
    Prof Didier Raoult, French physician and microbiologist specialising in infectious diseases, and one of the Top Scientists in the world with a H-Index of 212, on France's CNEWS: ------------------------- What Pfizer said was that there was only manipulated RNA, ...and that there was no DNA. However, there is a considerable amount of DNA in these vaccines. And we have measured it too. The quantity is huge. That is to say, what was supposed to be purified, the RNA was produced by bacteria in which a mini-chromosome had been inserted and it was necessary to purify this mini-chromosome and remove the DNA that had been used to make the RNA. This was not done.
    0 Comments 0 Shares 705 Views 2
  • Oleg Sherbakov - Physicists model chromosome folding, reveal how loops affect spatial organization of the genome:

    https://phys.org/news/2023-11-physicists-chromosome-reveal-loops-affect.html

    #ChromosomalLoop #ChromosomeFolding #Chromosome #DNAFolding #DNA #LoopExtrusion #Topology #HumanGenome #Genome #PolymerPhysics #Polymer #Physics #Genomics #Biology
    Oleg Sherbakov - Physicists model chromosome folding, reveal how loops affect spatial organization of the genome: https://phys.org/news/2023-11-physicists-chromosome-reveal-loops-affect.html #ChromosomalLoop #ChromosomeFolding #Chromosome #DNAFolding #DNA #LoopExtrusion #Topology #HumanGenome #Genome #PolymerPhysics #Polymer #Physics #Genomics #Biology
    PHYS.ORG
    Physicists model chromosome folding, reveal how loops affect spatial organization of the genome
    Human chromosomes are long polymer chains that store genetic information. The nucleus of each cell contains the entire human genome (DNA) encoded on 46 chromosomes with a total length of about 2 meters. To fit into the microscopic cell nucleus and at the same time provide constant access to genetic information, chromosomes are folded in the nucleus in a special, predetermined way. DNA folding is an urgent task at the intersection of polymer physics and systems biology.
    0 Comments 0 Shares 1756 Views
  • Pandemic of the Glioblastomas?
    The herd culling mRNA goodness is packaged in lipid nanoparticles which are able to cross the blood brain barrier...you know...for the Dangerous Germs that were murdering the world from the pangolins

    Sage Hana

    Promo Code: Conspiracy Sarah

    Paging all Oncologists and Glioblastoma Specialists.

    Are you seeing an uptick of cases?

    From my board, a comment from Kanada unrelated to the below anecdata from Sarah regarding a Love Canal cluster of events and deaths in Atlanta, home of the lovely CDC.

    Speaking of turbo cancer: spent the weekend taking care of my cousin (64, previously in excellent health) who had the injectables two years ago and then the boosters and is now in a near vegetative state, due to turbo glioblastoma. I sat with him this weekend so his wife could go do things like grocery shopping. The decline in this formerly brilliant lawyer/outdoorsman is shocking. And I KNOW it was the injectables.


    E’s brother died of a heart attack. Her friend of a glioblastoma.

    Two clients in the studio have been recently diagnosed with cancer, and currently in treatment. One has a sister who was diagnosed with endometrial cancer at the same time. Cancer does not run in their family.

    H has a CT to look at a cyst on her kidney.

    One client with fibroids bleeding out.

    Just got another glioblastoma call...😔 D's aunt...That's #6 for glioblastoma in my immediate circle.

    G's customer just diagnosed with glioblastoma - 6wks ago...discharged from hospital, sent home to wait to die. Now deceased.


    Glioblastoma (GBM) is a malignant grade 4 tumor that is predominantly made up of abnormal astrocytic cells, but also contains a mix of different cell types (including blood vessels) and areas of dead cells (necrosis). It is the most common primary brain cancer, with around 12,000 cases diagnosed in the United States each year.1 GBM is a fast-growing and aggressive brain tumor that invades nearby regions of the brain but generally does not spread to distant organs.0 Initial signs and symptoms of glioblastoma are nonspecific and may include headaches, personality changes, nausea, and symptoms similar to those of a stroke. Symptoms often worsen rapidly and may progress to unconsciousness.2


    Glioblastoma (GBM)

    Glioblastomas (also called GBM) are malignant (cancerous) grade 4 tumors. The tumor is predominantly made up of abnormal astrocytic cells, but also contains a mix of different cell types (including blood vessels) and areas of dead cells (necrosis). Glioblastomas are diffusely infiltrative and invade nearby regions of the brain. They can also sometimes spread to the opposite side of the brain through connection fibers (corpus callosum) or the ventricular system. It is exceedingly rare for glioblastomas to spread outside of the brain and spinal cord.

    Glioblastomas commonly arise de novo, meaning they begin as a grade 4 tumor with no evidence of a lower-grade precursor. De novo tumors are the most common form of glioblastoma. They tend to be more aggressive and are more common in patients 60 years of age or older, though younger patients may also be affected. Alternatively, secondary glioblastomas may progress from a lower-grade astrocytic tumors (grade 2 or 3) and evolve into grade 4 tumors over time. In general, these tumors tend to be slower growing initially, but can progressively become aggressive.

    In 2021 the World Health Organization (WHO) updated CNS tumor classifications, incorporating new knowledge gained from additional molecular markers and new diagnostic techniques. What used to be classified as Glioblastoma, IDH mutant is now classified as Astrocytoma, IDH mutant, grade 4. For information on Astrocytoma, IDH mutant, grade 4, please see our web page on Astrocytoma (Adult type). Glioblastomas are now classified as Astrocytoma IDH-wildtype tumors with at least one of the following: microvascular proliferation, necrosis, EGFR amplification, TERT promoter mutation, or combined gain of chromosome 7/loss of chromosome 10 copy number changes.

    Location

    Glioblastoma is most commonly found in the frontal lobe, followed by the temporal, parietal, and occipital lobes.

    Symptoms

    Patients with glioblastomas develop symptoms rapidly due to mass effect from the tumor itself or from the fluid surrounding the tumor that causes further brain swelling (edema). Common presenting symptoms at diagnosis include:

    Seizures

    Severe headaches

    Memory and language problems

    Changes in personality and behavior

    Muscle weakness or paralysis

    Fatigue

    Issues with coordination

    Speech, hearing, and vision problems

    Other symptoms may occur depending on the size and location of the tumor.

    Treatment

    Glioblastomas can be difficult to treat for the following reasons:

    They are fast-growing and invade nearby brain tissue, making 100% removal nearly impossible.

    The blood-brain barrier prevents certain treatments from being able to reach the tumor and be effective.

    They have many different types of tumor cells (heterogeneous) and can change over time, which makes them difficult to treat.

    Because of this, the treatment plan for glioblastoma may combine several approaches, including surgery, radiation therapy, chemotherapy, clinical trials, Tumor Treating Fields (TTFields), and targeted therapies.

    Surgery is often the first step in treating glioblastoma. Surgery allows the medical team to get a biopsy and make a diagnosis, relieve pressure on the brain, and safely remove as much tumor as possible. Glioblastomas are diffuse and have finger-like tentacles that infiltrate the brain, which makes them very difficult to remove completely. This is particularly true when the tumors are growing near important regions of the brain that control functions such as language and movement/coordination.


    More anecdotal evidence.

    Someone one degree of separation from me had a tumor behind her eye.

    It was excruciating.

    Tumor was removed.

    It came back.

    Yes.

    Got the shots. Hubs is a doc.

    The topic is not open for discussion as to the nature of the tumor.


    As I’ve said a million times, me no STEM.

    But I understand the concept of Dual Use.


    I have a terrible feeling that we just getting started, y’all.

    I see you, Monster.

    Or I think I do.


    related:

    Turbo-Cancer: "It feels like I'm watching people being killed and there is little I can do."

    Read full story

    Rah-rah, SH! WE like! Bad shit happened. Mistakes were not made! Chaaarrrrgggeeeeee!!!

    SPAR the marks. Make them feel heard.

    Whoa…

    I mean, no! Not like this, though! Don’t call all the numbers out the chute.

    Don’t take my Wilson the Volleyball away from me.

    Check the (mRNA) Dates

    Check the (mRNA) Dates
    Promo Code Teresa L. for inspiring me to check the dates on two three posts. April 19, 2023 “mRNA Off to a Bad Start but Future May be Brighter” By Peter A. McCullough, MD, MPH We all have the tendency to paint issues with a broad brush. That is to see things one way for intellectual simplicity. “All pharmaceuticals are bad” or “I don’t trust any vaccine.” …

    Read full story

    WEFFIE Agenda Good Cop Elon Musk: "I need to emphasize that accelerating synthetic mRNA technology was another silver lining. It is a revolution in medicine, like going from analog to digital."

    WEFFIE Agenda Good Cop Elon Musk: "I need to emphasize that accelerating synthetic mRNA technology was another silver lining. It is a revolution in medicine, like going from analog to digital."
    Good Cop to the Bad Cop Context:

    Read full story


    Anyway, I am in over my head, but if any Shih Tzu Detectives have intel on Glioblastomas rising or not, or Turbo Cancers rising or not…spill.

    I have a sense that there will be shenanigans with the records and coding but then again, I see phantoms everywhere.

    There is a phantom in my kitchen right now.


    https://ko-fi.com/sagehanaproductions64182

    https://www.buymeacoffee.com/sagehanaJ


    FALSIFIED SCIENTIFIC RESEARCH

    Somewhere in this connection, then, was the statement admitting that some scientific research data could be - and indeed has been - falsified in order to bring about desired results. And here was said, "People don't ask the right questions. Some people are too trusting."

    Now this was an interesting statement because the speaker and the audience all being doctors of medicine and supposedly very objectively, dispassionately scientific and science being the be all and end-all ... well to falsify scientific research data in that setting is like blasphemy in the church ... you just don't do that.

    Anyhow, out of all of this was to come the New International Governing Body, probably to come through the U.N . and with a World Court, but not necessarily through those structures. It could be brought about in other ways. Acceptance of the U.N . at that time was seen as not being as wide as was hoped. Efforts would continue to give the United Nations increasing importance. People would be more and more used to the idea of relinquishing some national sovereignty.


    SUPPRESSING CANCER CURES AS A MEANS OF POPULATION CONTROL

    Cancer. He said. "We can cure almost every cancer right now. Information is on file in the Rockefeller Institute, if it's ever decided that it should be released. But consider - if people stop dying of cancer, how rapidly we would become overpopulated. You may as well die of cancer as something else."

    Efforts at cancer treatment would be geared more toward comfort than toward cure. There was some statement that ultimately the cancer cures which were being hidden in the Rockefeller Institute would come to light because independent researchers might bring them out, despite these efforts to suppress them. But at least for the time being, letting people die of cancer was a good thing to do because it would slow down the problem of overpopulation.
    Pandemic of the Glioblastomas? The herd culling mRNA goodness is packaged in lipid nanoparticles which are able to cross the blood brain barrier...you know...for the Dangerous Germs that were murdering the world from the pangolins Sage Hana Promo Code: Conspiracy Sarah Paging all Oncologists and Glioblastoma Specialists. Are you seeing an uptick of cases? From my board, a comment from Kanada unrelated to the below anecdata from Sarah regarding a Love Canal cluster of events and deaths in Atlanta, home of the lovely CDC. Speaking of turbo cancer: spent the weekend taking care of my cousin (64, previously in excellent health) who had the injectables two years ago and then the boosters and is now in a near vegetative state, due to turbo glioblastoma. I sat with him this weekend so his wife could go do things like grocery shopping. The decline in this formerly brilliant lawyer/outdoorsman is shocking. And I KNOW it was the injectables. E’s brother died of a heart attack. Her friend of a glioblastoma. Two clients in the studio have been recently diagnosed with cancer, and currently in treatment. One has a sister who was diagnosed with endometrial cancer at the same time. Cancer does not run in their family. H has a CT to look at a cyst on her kidney. One client with fibroids bleeding out. Just got another glioblastoma call...😔 D's aunt...That's #6 for glioblastoma in my immediate circle. G's customer just diagnosed with glioblastoma - 6wks ago...discharged from hospital, sent home to wait to die. Now deceased. Glioblastoma (GBM) is a malignant grade 4 tumor that is predominantly made up of abnormal astrocytic cells, but also contains a mix of different cell types (including blood vessels) and areas of dead cells (necrosis). It is the most common primary brain cancer, with around 12,000 cases diagnosed in the United States each year.1 GBM is a fast-growing and aggressive brain tumor that invades nearby regions of the brain but generally does not spread to distant organs.0 Initial signs and symptoms of glioblastoma are nonspecific and may include headaches, personality changes, nausea, and symptoms similar to those of a stroke. Symptoms often worsen rapidly and may progress to unconsciousness.2 Glioblastoma (GBM) Glioblastomas (also called GBM) are malignant (cancerous) grade 4 tumors. The tumor is predominantly made up of abnormal astrocytic cells, but also contains a mix of different cell types (including blood vessels) and areas of dead cells (necrosis). Glioblastomas are diffusely infiltrative and invade nearby regions of the brain. They can also sometimes spread to the opposite side of the brain through connection fibers (corpus callosum) or the ventricular system. It is exceedingly rare for glioblastomas to spread outside of the brain and spinal cord. Glioblastomas commonly arise de novo, meaning they begin as a grade 4 tumor with no evidence of a lower-grade precursor. De novo tumors are the most common form of glioblastoma. They tend to be more aggressive and are more common in patients 60 years of age or older, though younger patients may also be affected. Alternatively, secondary glioblastomas may progress from a lower-grade astrocytic tumors (grade 2 or 3) and evolve into grade 4 tumors over time. In general, these tumors tend to be slower growing initially, but can progressively become aggressive. In 2021 the World Health Organization (WHO) updated CNS tumor classifications, incorporating new knowledge gained from additional molecular markers and new diagnostic techniques. What used to be classified as Glioblastoma, IDH mutant is now classified as Astrocytoma, IDH mutant, grade 4. For information on Astrocytoma, IDH mutant, grade 4, please see our web page on Astrocytoma (Adult type). Glioblastomas are now classified as Astrocytoma IDH-wildtype tumors with at least one of the following: microvascular proliferation, necrosis, EGFR amplification, TERT promoter mutation, or combined gain of chromosome 7/loss of chromosome 10 copy number changes. Location Glioblastoma is most commonly found in the frontal lobe, followed by the temporal, parietal, and occipital lobes. Symptoms Patients with glioblastomas develop symptoms rapidly due to mass effect from the tumor itself or from the fluid surrounding the tumor that causes further brain swelling (edema). Common presenting symptoms at diagnosis include: Seizures Severe headaches Memory and language problems Changes in personality and behavior Muscle weakness or paralysis Fatigue Issues with coordination Speech, hearing, and vision problems Other symptoms may occur depending on the size and location of the tumor. Treatment Glioblastomas can be difficult to treat for the following reasons: They are fast-growing and invade nearby brain tissue, making 100% removal nearly impossible. The blood-brain barrier prevents certain treatments from being able to reach the tumor and be effective. They have many different types of tumor cells (heterogeneous) and can change over time, which makes them difficult to treat. Because of this, the treatment plan for glioblastoma may combine several approaches, including surgery, radiation therapy, chemotherapy, clinical trials, Tumor Treating Fields (TTFields), and targeted therapies. Surgery is often the first step in treating glioblastoma. Surgery allows the medical team to get a biopsy and make a diagnosis, relieve pressure on the brain, and safely remove as much tumor as possible. Glioblastomas are diffuse and have finger-like tentacles that infiltrate the brain, which makes them very difficult to remove completely. This is particularly true when the tumors are growing near important regions of the brain that control functions such as language and movement/coordination. More anecdotal evidence. Someone one degree of separation from me had a tumor behind her eye. It was excruciating. Tumor was removed. It came back. Yes. Got the shots. Hubs is a doc. The topic is not open for discussion as to the nature of the tumor. As I’ve said a million times, me no STEM. But I understand the concept of Dual Use. I have a terrible feeling that we just getting started, y’all. I see you, Monster. Or I think I do. related: Turbo-Cancer: "It feels like I'm watching people being killed and there is little I can do." Read full story Rah-rah, SH! WE like! Bad shit happened. Mistakes were not made! Chaaarrrrgggeeeeee!!! SPAR the marks. Make them feel heard. Whoa… I mean, no! Not like this, though! Don’t call all the numbers out the chute. Don’t take my Wilson the Volleyball away from me. Check the (mRNA) Dates Check the (mRNA) Dates Promo Code Teresa L. for inspiring me to check the dates on two three posts. April 19, 2023 “mRNA Off to a Bad Start but Future May be Brighter” By Peter A. McCullough, MD, MPH We all have the tendency to paint issues with a broad brush. That is to see things one way for intellectual simplicity. “All pharmaceuticals are bad” or “I don’t trust any vaccine.” … Read full story WEFFIE Agenda Good Cop Elon Musk: "I need to emphasize that accelerating synthetic mRNA technology was another silver lining. It is a revolution in medicine, like going from analog to digital." WEFFIE Agenda Good Cop Elon Musk: "I need to emphasize that accelerating synthetic mRNA technology was another silver lining. It is a revolution in medicine, like going from analog to digital." Good Cop to the Bad Cop Context: Read full story Anyway, I am in over my head, but if any Shih Tzu Detectives have intel on Glioblastomas rising or not, or Turbo Cancers rising or not…spill. I have a sense that there will be shenanigans with the records and coding but then again, I see phantoms everywhere. There is a phantom in my kitchen right now. https://ko-fi.com/sagehanaproductions64182 https://www.buymeacoffee.com/sagehanaJ FALSIFIED SCIENTIFIC RESEARCH Somewhere in this connection, then, was the statement admitting that some scientific research data could be - and indeed has been - falsified in order to bring about desired results. And here was said, "People don't ask the right questions. Some people are too trusting." Now this was an interesting statement because the speaker and the audience all being doctors of medicine and supposedly very objectively, dispassionately scientific and science being the be all and end-all ... well to falsify scientific research data in that setting is like blasphemy in the church ... you just don't do that. Anyhow, out of all of this was to come the New International Governing Body, probably to come through the U.N . and with a World Court, but not necessarily through those structures. It could be brought about in other ways. Acceptance of the U.N . at that time was seen as not being as wide as was hoped. Efforts would continue to give the United Nations increasing importance. People would be more and more used to the idea of relinquishing some national sovereignty. SUPPRESSING CANCER CURES AS A MEANS OF POPULATION CONTROL Cancer. He said. "We can cure almost every cancer right now. Information is on file in the Rockefeller Institute, if it's ever decided that it should be released. But consider - if people stop dying of cancer, how rapidly we would become overpopulated. You may as well die of cancer as something else." Efforts at cancer treatment would be geared more toward comfort than toward cure. There was some statement that ultimately the cancer cures which were being hidden in the Rockefeller Institute would come to light because independent researchers might bring them out, despite these efforts to suppress them. But at least for the time being, letting people die of cancer was a good thing to do because it would slow down the problem of overpopulation.
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