• The Northern Virginia Astronomy Club hosted its annual Star Gaze outreach event at C.M. Crockett Park on Saturday, featuring Astronomy Bingo, a sky tour, telescopes on the observing field after sunset, and lectures by Woody Davis, Alan Goldberg, and Paul Derby. #StarGaze2024 #StarGaze #NOVAC #Virginia #NightSky #Astronomy
    The Northern Virginia Astronomy Club hosted its annual Star Gaze outreach event at C.M. Crockett Park on Saturday, featuring Astronomy Bingo, a sky tour, telescopes on the observing field after sunset, and lectures by Woody Davis, Alan Goldberg, and Paul Derby. #StarGaze2024 #StarGaze #NOVAC #Virginia #NightSky #Astronomy
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  • Malaria Parasites In “Vaccines” Target Placenta, Kill Babies In Utero
    April 23, 2022 by Dr. Ariyana Love
    By Dr. Ariyana Love, N.D.

    In a recent interview with Maria Zeee on Zeee Media, I discussed another very troubling discovery about the mRNA bioweapons technology. Maria Zeee asked me to shed more light on the Doherty Institutes involvement with the US biolabs in Ukraine.

    Russian reports revealed that 350 cryocontainers with blood serum samples were transferred from the Public Health Centre of the Ministry of Health of Ukraine to a reference laboratory for infectious diseases at the Doherty Institute in Australia.

    Under the guise of tackling Placental Malaria, the Doherty Institute has been directly involved in research using insects such as mosquitos and tics as bioweapons carriers. The Doherty Institute also developed a “vaccine” that uses a parasite to target the placenta of pregnant women to abort their babies in utero, under the pretext of “antibody research”.

    During the testing of this novel technology, mosquitos were developed as carriers of a genetically attenuated parasite called the P. falciparum which is the most deadly of the 5 Malaria causing parasites. The World Health Organization (WHO) and the U.S. Government were also directly involved in this research to “immunize” via mosquito bite using radiation-attenuated Sporozoites.

    In May of 2021, a Bill Gates-funded firm in the wild.

    Clinical trials conducted by the WHO in 2020, used 11 human volunteers who were “immunized” with more than 1000 bites by irradiated mosquitos infected by Sporozoites (Spz) from the P. falciparum NF54 strain or 3D7/NF54 clone.

    The female Anopheles mosquito inject a minimum of Sporozoites (Spz) (~ 100) during its bite. It was tested on adolescents, children and infants aged 6 months old. 1 out of the 6 volunteers developed parasitaemia 12 days after exposure. Parasitaemia means parasites in the blood.

    The parasite “vaccines” use radiation-attenuated Sporozoite, administered under drug coverage. Genetically-attenuated Sporozoite “vaccines” and recombinant protein “vaccines” (RTS,S and R21) and recombinant viral vectors “vaccines” (Chad63 MVA ME-TRAP, CSVAC, ChAd63 METRAP and MVA METRAP with the matrix-M adjuvant) are all used.

    Sporozoite recombinant proteins, DNA or viral vectored protein fragments (mRNA) and attenuated Sporozoite “vaccines” induce malaria reactive CD4+ and CD8+ T-lymphocyte counts. Radiation-attenuated Sporozoite (RAS), genetically-attenuated parasite (GAP) and Sporozoite are administered under drug coverage, according to the WHO study. Here’s another WHO study from 2021.

    By 2021, they had a P. falciparum Sporozoite (PfSPZ) “vaccine” as the main candidate containing live, radiation-attenuated, whole, aseptic and metabolically active Sporozoite which have been isolated from the salivary glands of mosquitos infected by P. falciparum. They tested their novel “vaccine” on infants in Kenya.

    Another study conducted by the NIAID in 2022, used Malian children 6-10 years old and injected them with three doses of the PfSpz “vaccine” to induce an “infection” by “parasitic disease” of a “vector borne disease” using the P. falciparum.

    Another study in 2021 carried out by the U.S. Government, experimented on 336 infants aged 5-12 months, in Kenya, inoculating them with the P. falciparum “vaccine”. This is not in fact a “vaccine” but a weapons system for the murder of babies in utero and this is a bioweapon which is transmissible to others, according to the WHO research.

    In addition, the WHO’s P. falciparum research helped in the development of monoclonal antibodies. In fact, the P. falciparum parasite is a critical component in the monoclonal antibodies bioweapon system.

    Please also see: Monoclonal Antibodies Is Experimental Gene Therapy – Patent Review

    PATENT

    The PRIMVAC “vaccine” candidate was in government trials in 2016. By 2020, the PRIMVAC “vaccine” adjuvanted with Alhydrogel was in clinical trials. The Alhydrogel patent shows unsafe levels of aluminum and other heavy metals.

    A VAR2CSA plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) patent for a synthetic protein was registered in December, 2014. The VAR2CSA “vaccine” is owned by the U.S. Government.

    The CDC is also involved in this VAR2CSA bioweapons development.

    STERILIZATION OF THE NATIONS

    Children’s Health Defence reported in August that the Covid-19 injections are dangerous for mothers and babies. According to former Chief Scientist of Pfizer, Dr. Mike Yeadon, the injected ingredients is building up in the ovaries and attacking the placenta of pregnant women.

    A preliminary findings of mRNA Covid-19 vaccine safety in pregnant persons found that 4 out of 5 pregnant women are loosing their unborn baby to spontaneous abortions.

    A recent report released in March of this year, shows that fetal deaths due to “covid vaccines” are almost 2,000% greater than deaths associated with other vaccines.

    Below are a few highlights from the WHO study Plasmodium falciparum pre-erythrocytic stage vaccine development that I want to draw your attention to.

    RECOMBINANT VIRAL VECTOR “VACCINES”

    “Viral vectors represent promising tools for vaccine development, because they enable intracellular antigens to be expressed by increasing the ability to generate robust cytotoxic T-lymphocyte responses and proinflammatory interferon and cytokine production without the need for an adjuvant. However, there is great concern regarding their genotoxicity due to possible viral genome integration; this has led to many efforts aimed at finding a high level of safety and efficacy.”

    “Several viral, bacterial, and parasite vectors have been used in anti-malarial vaccine candidates; currently, many clinical trials are exploring their advantages to increase their potential and accelerate their use in vaccines.”

    CHAD63 MVA ME-TRAP

    “This anti-malarial vaccine was developed using chimpanzee adenovirus 63 (Chad63) and modified Vaccinia virus Ankara (MVA) into which were inserted genes encoding the thrombospondin-related adhesion protein (TRAP) multiple epitope (ME) chain.”

    “The ME-TRAP hybrid is thus a 2398 base pair (bp) insert encoding a single 789 aa-long peptide, covering the complete P. falciparum TRAP sequence, fused to a chain of 20 malaria T- and B-cell epitopes (14 targeting MHC class I, 3 MHC class II and 1 murine).”

    PCR

    “A trial involving adults in Senegal to assess vaccine efficacy using a polymerase chain reaction (PCR) assay was able to detect > 10 parasites/μl blood. PCR was positive for 12 out of 57 participants vaccinated with ChAd63 ME-TRAP with a booster dose of MVA ME-TRAP and 13 out of 58 control patients who received an anti-rabies vaccine were positive by PCR, giving 8% efficacy (which was not statistically significant). They thus grouped the results with the 67% efficacy obtained in a study in Kenya and, using Cox regression, showed 50% overall vaccine efficacy in both populations.”

    CSVAC

    “CSVAC, a vaccine from Chad63 and MVA to encode the P. falciparum CS protein, continued such line of research into plasmid DNA anti-malarial vaccines; the CS insert was a codon-optimized cDNA encoding the CS protein truncated at the C-terminal extreme thereby lacking 14 C-terminal aa and thus omitting the GPI anchor.”

    FUTURE DIRECTIONS

    “Nanovaccinology” with Self-Assembling Protein Nanoparticles (SAPNs)… The next major challenge concerns the host’s genetic variability and parasite proteins’ interaction with the human immune system.”

    “The choice of antigen to be used is quite complicated due to factors such as the parasite’s complex life-cycle involving two reproduction cycles (sexual and asexual), different development stages and two hosts (the Anopheles mosquito and human beings). All this can be added to the multiple invasion routes described so far for each of its target cells (hepatocytes and/or erythrocytes), the parasite’s ability to modify its gene expression and the genetic variability between P. falciparum circulating strains.”

    “The next major challenge concerns the host’s genetic variability, particularly major histocompatibility class II (MHCII) complex molecules exerting their mechanism by synthesizing proteins encoded by the HLA-DR regions β1*, β3*, β4* and β5* where the HLA-DR β1* region encodes more than 1500 genetic variants grouped into 16 allele families called HLA-DRβ1*01, *03, *04, *07, etc. Parasite proteins’ interaction with the human immune system should be analysed by predicting B and T epitopes (using NetMHCIIpan 3.2 or other predictors).”

    UPDATE: 6/6/2022

    Please see: Pfizer’s mRNA Vaccine Goes Into Liver Cells and Is Converted to DNA: Study


    https://ambassadorlove.blog/2022/04/23/malaria-parasites-in-vaccines-target-placenta-kill-babies-in-utero/
    Malaria Parasites In “Vaccines” Target Placenta, Kill Babies In Utero April 23, 2022 by Dr. Ariyana Love By Dr. Ariyana Love, N.D. In a recent interview with Maria Zeee on Zeee Media, I discussed another very troubling discovery about the mRNA bioweapons technology. Maria Zeee asked me to shed more light on the Doherty Institutes involvement with the US biolabs in Ukraine. Russian reports revealed that 350 cryocontainers with blood serum samples were transferred from the Public Health Centre of the Ministry of Health of Ukraine to a reference laboratory for infectious diseases at the Doherty Institute in Australia. Under the guise of tackling Placental Malaria, the Doherty Institute has been directly involved in research using insects such as mosquitos and tics as bioweapons carriers. The Doherty Institute also developed a “vaccine” that uses a parasite to target the placenta of pregnant women to abort their babies in utero, under the pretext of “antibody research”. During the testing of this novel technology, mosquitos were developed as carriers of a genetically attenuated parasite called the P. falciparum which is the most deadly of the 5 Malaria causing parasites. The World Health Organization (WHO) and the U.S. Government were also directly involved in this research to “immunize” via mosquito bite using radiation-attenuated Sporozoites. In May of 2021, a Bill Gates-funded firm in the wild. Clinical trials conducted by the WHO in 2020, used 11 human volunteers who were “immunized” with more than 1000 bites by irradiated mosquitos infected by Sporozoites (Spz) from the P. falciparum NF54 strain or 3D7/NF54 clone. The female Anopheles mosquito inject a minimum of Sporozoites (Spz) (~ 100) during its bite. It was tested on adolescents, children and infants aged 6 months old. 1 out of the 6 volunteers developed parasitaemia 12 days after exposure. Parasitaemia means parasites in the blood. The parasite “vaccines” use radiation-attenuated Sporozoite, administered under drug coverage. Genetically-attenuated Sporozoite “vaccines” and recombinant protein “vaccines” (RTS,S and R21) and recombinant viral vectors “vaccines” (Chad63 MVA ME-TRAP, CSVAC, ChAd63 METRAP and MVA METRAP with the matrix-M adjuvant) are all used. Sporozoite recombinant proteins, DNA or viral vectored protein fragments (mRNA) and attenuated Sporozoite “vaccines” induce malaria reactive CD4+ and CD8+ T-lymphocyte counts. Radiation-attenuated Sporozoite (RAS), genetically-attenuated parasite (GAP) and Sporozoite are administered under drug coverage, according to the WHO study. Here’s another WHO study from 2021. By 2021, they had a P. falciparum Sporozoite (PfSPZ) “vaccine” as the main candidate containing live, radiation-attenuated, whole, aseptic and metabolically active Sporozoite which have been isolated from the salivary glands of mosquitos infected by P. falciparum. They tested their novel “vaccine” on infants in Kenya. Another study conducted by the NIAID in 2022, used Malian children 6-10 years old and injected them with three doses of the PfSpz “vaccine” to induce an “infection” by “parasitic disease” of a “vector borne disease” using the P. falciparum. Another study in 2021 carried out by the U.S. Government, experimented on 336 infants aged 5-12 months, in Kenya, inoculating them with the P. falciparum “vaccine”. This is not in fact a “vaccine” but a weapons system for the murder of babies in utero and this is a bioweapon which is transmissible to others, according to the WHO research. In addition, the WHO’s P. falciparum research helped in the development of monoclonal antibodies. In fact, the P. falciparum parasite is a critical component in the monoclonal antibodies bioweapon system. Please also see: Monoclonal Antibodies Is Experimental Gene Therapy – Patent Review PATENT The PRIMVAC “vaccine” candidate was in government trials in 2016. By 2020, the PRIMVAC “vaccine” adjuvanted with Alhydrogel was in clinical trials. The Alhydrogel patent shows unsafe levels of aluminum and other heavy metals. A VAR2CSA plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) patent for a synthetic protein was registered in December, 2014. The VAR2CSA “vaccine” is owned by the U.S. Government. The CDC is also involved in this VAR2CSA bioweapons development. STERILIZATION OF THE NATIONS Children’s Health Defence reported in August that the Covid-19 injections are dangerous for mothers and babies. According to former Chief Scientist of Pfizer, Dr. Mike Yeadon, the injected ingredients is building up in the ovaries and attacking the placenta of pregnant women. A preliminary findings of mRNA Covid-19 vaccine safety in pregnant persons found that 4 out of 5 pregnant women are loosing their unborn baby to spontaneous abortions. A recent report released in March of this year, shows that fetal deaths due to “covid vaccines” are almost 2,000% greater than deaths associated with other vaccines. Below are a few highlights from the WHO study Plasmodium falciparum pre-erythrocytic stage vaccine development that I want to draw your attention to. RECOMBINANT VIRAL VECTOR “VACCINES” “Viral vectors represent promising tools for vaccine development, because they enable intracellular antigens to be expressed by increasing the ability to generate robust cytotoxic T-lymphocyte responses and proinflammatory interferon and cytokine production without the need for an adjuvant. However, there is great concern regarding their genotoxicity due to possible viral genome integration; this has led to many efforts aimed at finding a high level of safety and efficacy.” “Several viral, bacterial, and parasite vectors have been used in anti-malarial vaccine candidates; currently, many clinical trials are exploring their advantages to increase their potential and accelerate their use in vaccines.” CHAD63 MVA ME-TRAP “This anti-malarial vaccine was developed using chimpanzee adenovirus 63 (Chad63) and modified Vaccinia virus Ankara (MVA) into which were inserted genes encoding the thrombospondin-related adhesion protein (TRAP) multiple epitope (ME) chain.” “The ME-TRAP hybrid is thus a 2398 base pair (bp) insert encoding a single 789 aa-long peptide, covering the complete P. falciparum TRAP sequence, fused to a chain of 20 malaria T- and B-cell epitopes (14 targeting MHC class I, 3 MHC class II and 1 murine).” PCR “A trial involving adults in Senegal to assess vaccine efficacy using a polymerase chain reaction (PCR) assay was able to detect > 10 parasites/μl blood. PCR was positive for 12 out of 57 participants vaccinated with ChAd63 ME-TRAP with a booster dose of MVA ME-TRAP and 13 out of 58 control patients who received an anti-rabies vaccine were positive by PCR, giving 8% efficacy (which was not statistically significant). They thus grouped the results with the 67% efficacy obtained in a study in Kenya and, using Cox regression, showed 50% overall vaccine efficacy in both populations.” CSVAC “CSVAC, a vaccine from Chad63 and MVA to encode the P. falciparum CS protein, continued such line of research into plasmid DNA anti-malarial vaccines; the CS insert was a codon-optimized cDNA encoding the CS protein truncated at the C-terminal extreme thereby lacking 14 C-terminal aa and thus omitting the GPI anchor.” FUTURE DIRECTIONS “Nanovaccinology” with Self-Assembling Protein Nanoparticles (SAPNs)… The next major challenge concerns the host’s genetic variability and parasite proteins’ interaction with the human immune system.” “The choice of antigen to be used is quite complicated due to factors such as the parasite’s complex life-cycle involving two reproduction cycles (sexual and asexual), different development stages and two hosts (the Anopheles mosquito and human beings). All this can be added to the multiple invasion routes described so far for each of its target cells (hepatocytes and/or erythrocytes), the parasite’s ability to modify its gene expression and the genetic variability between P. falciparum circulating strains.” “The next major challenge concerns the host’s genetic variability, particularly major histocompatibility class II (MHCII) complex molecules exerting their mechanism by synthesizing proteins encoded by the HLA-DR regions β1*, β3*, β4* and β5* where the HLA-DR β1* region encodes more than 1500 genetic variants grouped into 16 allele families called HLA-DRβ1*01, *03, *04, *07, etc. Parasite proteins’ interaction with the human immune system should be analysed by predicting B and T epitopes (using NetMHCIIpan 3.2 or other predictors).” UPDATE: 6/6/2022 Please see: Pfizer’s mRNA Vaccine Goes Into Liver Cells and Is Converted to DNA: Study https://ambassadorlove.blog/2022/04/23/malaria-parasites-in-vaccines-target-placenta-kill-babies-in-utero/
    AMBASSADORLOVE.BLOG
    Malaria Parasites In “Vaccines” Target Placenta, Kill Babies In Utero
    By Dr. Ariyana Love, N.D. In a recent interview with Maria Zeee on Zeee Media, I discussed another very troubling discovery about the mRNA bioweapons technology. Maria Zeee asked me to shed more li…
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  • Air Vax — The Latest mRNA Delivered Into Lungs
    (Mercola)—Yale University researchers have developed a new airborne method for delivering mRNA right to your lungs. The team has also used the method to vaccinate mice intranasally,1 opening the door for human testing in the near future.

    While scientists are hailing the creation as an easy way to vaccinate the masses, critics wonder if the development of an airborne vaccine could be used for nefarious purposes, including covert bioenhancements,2 which have already been recommended in academic literature.3

    Yale Team Develops Airborne mRNA, Delivers It to Lungs

    In a study on mice, Yale scientists created polymer nanoparticles to encapsulate mRNA, making it inhalable so it can reach the lungs. Courtney Malo, editor with Science Translational Medicine, which published the study, explained:4

    “The ability to efficiently deliver mRNA to the lung would have applications for vaccine development, gene therapy, and more. Here, Suberi et al. showed that such mRNA delivery can be accomplished by encapsulating mRNAs of interest within optimized poly(amine-co-ester) polyplexes [nanoparticles].

    Polyplex-delivered mRNAs were efficiently translated into protein in the lungs of mice with limited evidence of toxicity. This platform was successfully applied as an intranasal SARS-CoV-2 vaccine, eliciting robust immune responses that conferred protection against subsequent viral challenge. These results highlight the potential of this delivery system for vaccine applications and beyond.”

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    The team, led by cellular and molecular physiologist Mark Saltzman, explained that the inhalable mRNA vaccine successfully protected against SARS-CoV-2, which “opens the door to delivering other messenger RNA (mRNA) therapeutics for gene replacement therapy and other treatments in the lungs.”5

    For the study, mice received two intranasal doses of nanoparticles carrying mRNA COVID-19 vaccines, which proved to be effective in the animals. In the past, lung-targeted mRNA therapies had trouble making it into the cells necessary to express the encoded protein, known as poor transfection efficiency.6

    Skyrocketing Food Prices Are Prompting Many Americans to Stock Up on Long-Term Storage Beef

    “The Saltzman group got around this hurdle in part by using a nanoparticle made from poly(amine-co-ester) polyplexes, or PACE, a biocompatible and highly customizable polymer,” a Yale University news release explained.7 In a previous study, Saltzman had tried a “prime and spike” system to deliver COVID-19 shots, which involved injecting mRNA shots into a muscle, then spraying spike proteins into the nose.8

    It turned out the injection portion may be unnecessary, and Saltzman has high hopes for the airborne delivery method, beyond vaccines:9

    “In the new report, there is no intramuscular injection. We just gave two doses, a prime and a boost, intranasally, and we got a highly protective immune response. But we also showed that, generally, you can deliver different kinds of mRNA. So it’s not just good for a vaccine, but potentially also good for gene replacement therapy in diseases like cystic fibrosis and gene editing.

    We used a vaccine example to show that it works, but it opens the door to doing all these other kinds of interventions.”

    Air Vax Could ‘Radically Change’ How People Are Vaccinated

    MORE NEWS: Data Analyst Says Gold Will Be the “New Reserve Asset” — Time to Get the Gold Guide

    Saltzman says this “new method of delivery could ‘radically change the way people are vaccinated,’” making it easier to vaccinate people in remote areas or those who are afraid of needles.10 But that’s not all. An airborne vaccine makes it possible to rapidly disseminate it across a population.

    By releasing the vaccine in the air, there’s no need to inject each person individually — which is not only time-consuming but difficult if an individual objects to the shot. This isn’t the case with an airborne vaccine, which can be released into the air without consent or even the public’s knowledge.

    A similar strategy is being used with mRNA in shrimp, which are too small and numerous to be injected individually. Instead, an oral “nanovaccine” was created to stop the spread of a virus. Shai Ufaz, chief executive officer of ViAqua, which developed the technology, stated:11

    “Oral delivery is the holy grail of aquaculture health development due to both the impossibility of vaccinating individual shrimp and its ability to substantially bring down the operational costs of disease management while improving outcomes …”

    While the Yale scientists are targeting an intranasal mRNA product, the outcome is the same — get as many exposed as possible with the least amount of cost and effort. According to the Yale study:12

    “An inhalable platform for messenger RNA (mRNA) therapeutics would enable minimally invasive and lung-targeted delivery for a host of pulmonary diseases. Development of lung-targeted mRNA therapeutics has been limited by poor transfection efficiency and risk of vehicle-induced pathology.

    Here, we report an inhalable polymer-based vehicle for delivery of therapeutic mRNAs to the lung. We optimized biodegradable poly(amine-co-ester) (PACE) polyplexes [nanoparticles] for mRNA delivery using end-group modifications and polyethylene glycol. These polyplexes achieved high transfection of mRNA throughout the lung, particularly in epithelial and antigen-presenting cells.

    We applied this technology to develop a mucosal vaccine for severe acute respiratory syndrome coronavirus 2 and found that intranasal vaccination with spike protein–encoding mRNA polyplexes induced potent cellular and humoral adaptive immunity and protected susceptible mice from lethal viral challenge. Together, these results demonstrate the translational potential of PACE polyplexes for therapeutic delivery of mRNA to the lungs.”

    US Government Has History of Bioweapons Release

    When you put the pieces of the puzzle together, a disturbing picture emerges. As reported by The Epoch Times, we have a history of the U.S. government taking extreme measures to mandate and promote COVID-19 shots to the public. Now, researchers have developed an airborne mRNA vaccine, offering a vehicle by which to rapidly vaccinate the masses without their knowledge or consent.13

    Is there proof that the government or another entity has plans to covertly release an air vax on the population? No. But there is a history of it carrying out secret bioweapon simulations on Americans. In 1950, the U.S. Navy sprayed Serratia marcescens bacteria into the air near San Francisco over a period of six days.

    MORE NEWS: Washington State Is ‘Ground Zero’ for EV Charging Port Thefts

    Dubbed “Operation Sea Spray,” the project was intended to determine how susceptible the city was to a bioweapon attack. Serratia marcescens turns whatever it touches bright red, making it easy to track. It spread throughout the city, as residents inhaled the microbes from the air. While the U.S. military initially thought Serratia marcescens wouldn’t harm humans, an outbreak occurred, with some developing urinary tract infections as a result.

    At least one person died “and some have suggested that the release forever changed the area’s microbial ecology,” Smithsonian Magazine reported.14 This wasn’t an isolated incident, as the U.S. government carried out many other experiments across the U.S. over the next 20 years.15 So, while it’s disturbing to think of an air vax experiment being conducted on an unsuspecting public, it’s not unprecedented.

    Bioethics Study Promotes Covert, Compulsory Bioenhancement

    Adding to the story is academic endorsement of the use of compulsory, covert bioenhancements. Writing in the journal Bioethics,16 Parker Crutchfield with Western Michigan University, Homer Stryker M.D. School of Medicine, discusses moral bioenhancements, which refers to the use of biomedical means to trigger moral improvements.

    Drug treatments, including vaccines, and genetic engineering are potential examples of bioenhancements.17 Further, according to Crutchfield:18

    “It is necessary to morally bioenhance the population in order to prevent ultimate harm. Moral bioenhancement is the potential practice of influencing a person’s moral behavior by way of biological intervention upon their moral attitudes, motivations, or dispositions.

    The technology that may permit moral bioenhancement is on the scale between nonexistent and nascent, but common examples of potential interventions include infusing water supplies with pharmaceuticals that enhance empathy or altruism or otherwise intervening on a person’s emotions or motivations, in an attempt to influence the person’s moral behavior.”

    Some argue that moral bioenhancements should be compulsory for the greater good. Crutchfield believes this doesn’t go far enough. He also wants them to be covert:19

    “I take this argument one step further, arguing that if moral bioenhancement ought to be compulsory, then its administration ought to be covert rather than overt. This is to say that it is morally preferable for compulsory moral bioenhancement to be administered without the recipients knowing that they are receiving the enhancement.”

    MORE NEWS: Suspect Arrested After Shooting Houston Police Officer Amid Hurricane Recovery

    He even goes so far as to suggest “a covert compulsory program promotes values such as liberty, utility, equality and autonomy better than an overt program does.”20 So here we have evidence of academic support for covertly releasing drugs and other bioenhancements onto the public. This, combined with the creation of an airborne mRNA vaccine and the government’s history of experimenting on the public, paints an unsettling picture of the future.

    Problems With mRNA COVID Shots Persist

    Aside from the concerns of airborne delivery, mRNA COVID-19 shots are associated with significant risks — no matter how you’re exposed. People ages 65 and older who received Pfizer’s updated (bivalent) COVID-19 booster shot may be at increased risk of stroke, according to an announcement made by the U.S. Centers for Disease Control and Prevention and the Food and Drug Administration.21

    Further, a large study from Israel22 revealed that Pfizer’s COVID-19 mRNA jab is associated with a threefold increased risk of myocarditis,23 leading to the condition at a rate of 1 to 5 events per 100,000 persons.24 Other elevated risks were also identified following the COVID jab, including lymphadenopathy (swollen lymph nodes), appendicitis and herpes zoster infection.25

    At least 16,183 people also say they’ve developed tinnitus after receiving a COVID-19 shot.26 The reports were filed with the CDC’s Vaccine Adverse Event Reporting System (VAERS) database. But considering only between 1%27 and 10%28 of adverse reactions are ever reported to VAERS, the actual number is likely much higher.

    It’s because of risks like these that informed consent is essential for any medical procedure, including vaccinations. The development of airborne mRNA jabs, however, makes the possibility of informed consent being taken away all the more real.

    1, 4 Science Translational Medicine August 16, 2023, Vol 15, Issue 709
    2, 13 The Epoch Times September 5, 2023
    3 Bioethics. 2019 Jan;33(1):112-121. doi: 10.1111/bioe.12496. Epub 2018 Aug 29
    5, 6, 7, 8, 9 Yale School of Engineering & Applied Science, News & Events August 16, 2023
    10 Bitchute, Truther’s Lair September 5, 2023, 5:09
    11 Fish Farmer September 5, 2023
    12 Science Translational Medicine August 16, 2023, Vol 15, Issue 709, Abstract
    14, 15 Smithsonian Magazine July 6, 2015
    16, 18 Bioethics. 2019 Jan;33(1):112-121. doi: 10.1111/bioe.12496. Epub 2018 Aug 29., Intro
    17 Topoi volume 38, pages 1–5 (2019)
    19, 20 Bioethics. 2019 Jan;33(1):112-121. doi: 10.1111/bioe.12496. Epub 2018 Aug 29., Abstract
    21 U.S. FDA January 13, 2023
    22, 24, 25 The New England Journal of Medicine August 25, 2021
    23 MedPage Today August 25, 2021
    26 NBC News April 23, 2023
    27 Harvard Pilgrim Health Care report submitted to the U.S. Department of Health and Human Services, 2011, Page 6
    28 BMJ 2005;330:433
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    https://discernreport.com/air-vax-the-latest-mrna-delivered-into-lungs/
    Air Vax — The Latest mRNA Delivered Into Lungs (Mercola)—Yale University researchers have developed a new airborne method for delivering mRNA right to your lungs. The team has also used the method to vaccinate mice intranasally,1 opening the door for human testing in the near future. While scientists are hailing the creation as an easy way to vaccinate the masses, critics wonder if the development of an airborne vaccine could be used for nefarious purposes, including covert bioenhancements,2 which have already been recommended in academic literature.3 Yale Team Develops Airborne mRNA, Delivers It to Lungs In a study on mice, Yale scientists created polymer nanoparticles to encapsulate mRNA, making it inhalable so it can reach the lungs. Courtney Malo, editor with Science Translational Medicine, which published the study, explained:4 “The ability to efficiently deliver mRNA to the lung would have applications for vaccine development, gene therapy, and more. Here, Suberi et al. showed that such mRNA delivery can be accomplished by encapsulating mRNAs of interest within optimized poly(amine-co-ester) polyplexes [nanoparticles]. Polyplex-delivered mRNAs were efficiently translated into protein in the lungs of mice with limited evidence of toxicity. This platform was successfully applied as an intranasal SARS-CoV-2 vaccine, eliciting robust immune responses that conferred protection against subsequent viral challenge. These results highlight the potential of this delivery system for vaccine applications and beyond.” Skyrocketing Food Prices Are Prompting Many Americans to Stock Up on Long-Term Storage Beef MORE NEWS: Stephanopoulos Caught on Camera After Biden Interview: ‘I Don’t Think He Can Serve Four More Years’ The team, led by cellular and molecular physiologist Mark Saltzman, explained that the inhalable mRNA vaccine successfully protected against SARS-CoV-2, which “opens the door to delivering other messenger RNA (mRNA) therapeutics for gene replacement therapy and other treatments in the lungs.”5 For the study, mice received two intranasal doses of nanoparticles carrying mRNA COVID-19 vaccines, which proved to be effective in the animals. In the past, lung-targeted mRNA therapies had trouble making it into the cells necessary to express the encoded protein, known as poor transfection efficiency.6 Skyrocketing Food Prices Are Prompting Many Americans to Stock Up on Long-Term Storage Beef “The Saltzman group got around this hurdle in part by using a nanoparticle made from poly(amine-co-ester) polyplexes, or PACE, a biocompatible and highly customizable polymer,” a Yale University news release explained.7 In a previous study, Saltzman had tried a “prime and spike” system to deliver COVID-19 shots, which involved injecting mRNA shots into a muscle, then spraying spike proteins into the nose.8 It turned out the injection portion may be unnecessary, and Saltzman has high hopes for the airborne delivery method, beyond vaccines:9 “In the new report, there is no intramuscular injection. We just gave two doses, a prime and a boost, intranasally, and we got a highly protective immune response. But we also showed that, generally, you can deliver different kinds of mRNA. So it’s not just good for a vaccine, but potentially also good for gene replacement therapy in diseases like cystic fibrosis and gene editing. We used a vaccine example to show that it works, but it opens the door to doing all these other kinds of interventions.” Air Vax Could ‘Radically Change’ How People Are Vaccinated MORE NEWS: Data Analyst Says Gold Will Be the “New Reserve Asset” — Time to Get the Gold Guide Saltzman says this “new method of delivery could ‘radically change the way people are vaccinated,’” making it easier to vaccinate people in remote areas or those who are afraid of needles.10 But that’s not all. An airborne vaccine makes it possible to rapidly disseminate it across a population. By releasing the vaccine in the air, there’s no need to inject each person individually — which is not only time-consuming but difficult if an individual objects to the shot. This isn’t the case with an airborne vaccine, which can be released into the air without consent or even the public’s knowledge. A similar strategy is being used with mRNA in shrimp, which are too small and numerous to be injected individually. Instead, an oral “nanovaccine” was created to stop the spread of a virus. Shai Ufaz, chief executive officer of ViAqua, which developed the technology, stated:11 “Oral delivery is the holy grail of aquaculture health development due to both the impossibility of vaccinating individual shrimp and its ability to substantially bring down the operational costs of disease management while improving outcomes …” While the Yale scientists are targeting an intranasal mRNA product, the outcome is the same — get as many exposed as possible with the least amount of cost and effort. According to the Yale study:12 “An inhalable platform for messenger RNA (mRNA) therapeutics would enable minimally invasive and lung-targeted delivery for a host of pulmonary diseases. Development of lung-targeted mRNA therapeutics has been limited by poor transfection efficiency and risk of vehicle-induced pathology. Here, we report an inhalable polymer-based vehicle for delivery of therapeutic mRNAs to the lung. We optimized biodegradable poly(amine-co-ester) (PACE) polyplexes [nanoparticles] for mRNA delivery using end-group modifications and polyethylene glycol. These polyplexes achieved high transfection of mRNA throughout the lung, particularly in epithelial and antigen-presenting cells. We applied this technology to develop a mucosal vaccine for severe acute respiratory syndrome coronavirus 2 and found that intranasal vaccination with spike protein–encoding mRNA polyplexes induced potent cellular and humoral adaptive immunity and protected susceptible mice from lethal viral challenge. Together, these results demonstrate the translational potential of PACE polyplexes for therapeutic delivery of mRNA to the lungs.” US Government Has History of Bioweapons Release When you put the pieces of the puzzle together, a disturbing picture emerges. As reported by The Epoch Times, we have a history of the U.S. government taking extreme measures to mandate and promote COVID-19 shots to the public. Now, researchers have developed an airborne mRNA vaccine, offering a vehicle by which to rapidly vaccinate the masses without their knowledge or consent.13 Is there proof that the government or another entity has plans to covertly release an air vax on the population? No. But there is a history of it carrying out secret bioweapon simulations on Americans. In 1950, the U.S. Navy sprayed Serratia marcescens bacteria into the air near San Francisco over a period of six days. MORE NEWS: Washington State Is ‘Ground Zero’ for EV Charging Port Thefts Dubbed “Operation Sea Spray,” the project was intended to determine how susceptible the city was to a bioweapon attack. Serratia marcescens turns whatever it touches bright red, making it easy to track. It spread throughout the city, as residents inhaled the microbes from the air. While the U.S. military initially thought Serratia marcescens wouldn’t harm humans, an outbreak occurred, with some developing urinary tract infections as a result. At least one person died “and some have suggested that the release forever changed the area’s microbial ecology,” Smithsonian Magazine reported.14 This wasn’t an isolated incident, as the U.S. government carried out many other experiments across the U.S. over the next 20 years.15 So, while it’s disturbing to think of an air vax experiment being conducted on an unsuspecting public, it’s not unprecedented. Bioethics Study Promotes Covert, Compulsory Bioenhancement Adding to the story is academic endorsement of the use of compulsory, covert bioenhancements. Writing in the journal Bioethics,16 Parker Crutchfield with Western Michigan University, Homer Stryker M.D. School of Medicine, discusses moral bioenhancements, which refers to the use of biomedical means to trigger moral improvements. Drug treatments, including vaccines, and genetic engineering are potential examples of bioenhancements.17 Further, according to Crutchfield:18 “It is necessary to morally bioenhance the population in order to prevent ultimate harm. Moral bioenhancement is the potential practice of influencing a person’s moral behavior by way of biological intervention upon their moral attitudes, motivations, or dispositions. The technology that may permit moral bioenhancement is on the scale between nonexistent and nascent, but common examples of potential interventions include infusing water supplies with pharmaceuticals that enhance empathy or altruism or otherwise intervening on a person’s emotions or motivations, in an attempt to influence the person’s moral behavior.” Some argue that moral bioenhancements should be compulsory for the greater good. Crutchfield believes this doesn’t go far enough. He also wants them to be covert:19 “I take this argument one step further, arguing that if moral bioenhancement ought to be compulsory, then its administration ought to be covert rather than overt. This is to say that it is morally preferable for compulsory moral bioenhancement to be administered without the recipients knowing that they are receiving the enhancement.” MORE NEWS: Suspect Arrested After Shooting Houston Police Officer Amid Hurricane Recovery He even goes so far as to suggest “a covert compulsory program promotes values such as liberty, utility, equality and autonomy better than an overt program does.”20 So here we have evidence of academic support for covertly releasing drugs and other bioenhancements onto the public. This, combined with the creation of an airborne mRNA vaccine and the government’s history of experimenting on the public, paints an unsettling picture of the future. Problems With mRNA COVID Shots Persist Aside from the concerns of airborne delivery, mRNA COVID-19 shots are associated with significant risks — no matter how you’re exposed. People ages 65 and older who received Pfizer’s updated (bivalent) COVID-19 booster shot may be at increased risk of stroke, according to an announcement made by the U.S. Centers for Disease Control and Prevention and the Food and Drug Administration.21 Further, a large study from Israel22 revealed that Pfizer’s COVID-19 mRNA jab is associated with a threefold increased risk of myocarditis,23 leading to the condition at a rate of 1 to 5 events per 100,000 persons.24 Other elevated risks were also identified following the COVID jab, including lymphadenopathy (swollen lymph nodes), appendicitis and herpes zoster infection.25 At least 16,183 people also say they’ve developed tinnitus after receiving a COVID-19 shot.26 The reports were filed with the CDC’s Vaccine Adverse Event Reporting System (VAERS) database. But considering only between 1%27 and 10%28 of adverse reactions are ever reported to VAERS, the actual number is likely much higher. It’s because of risks like these that informed consent is essential for any medical procedure, including vaccinations. The development of airborne mRNA jabs, however, makes the possibility of informed consent being taken away all the more real. 1, 4 Science Translational Medicine August 16, 2023, Vol 15, Issue 709 2, 13 The Epoch Times September 5, 2023 3 Bioethics. 2019 Jan;33(1):112-121. doi: 10.1111/bioe.12496. Epub 2018 Aug 29 5, 6, 7, 8, 9 Yale School of Engineering & Applied Science, News & Events August 16, 2023 10 Bitchute, Truther’s Lair September 5, 2023, 5:09 11 Fish Farmer September 5, 2023 12 Science Translational Medicine August 16, 2023, Vol 15, Issue 709, Abstract 14, 15 Smithsonian Magazine July 6, 2015 16, 18 Bioethics. 2019 Jan;33(1):112-121. doi: 10.1111/bioe.12496. Epub 2018 Aug 29., Intro 17 Topoi volume 38, pages 1–5 (2019) 19, 20 Bioethics. 2019 Jan;33(1):112-121. doi: 10.1111/bioe.12496. Epub 2018 Aug 29., Abstract 21 U.S. FDA January 13, 2023 22, 24, 25 The New England Journal of Medicine August 25, 2021 23 MedPage Today August 25, 2021 26 NBC News April 23, 2023 27 Harvard Pilgrim Health Care report submitted to the U.S. Department of Health and Human Services, 2011, Page 6 28 BMJ 2005;330:433 Skyrocketing Food Prices Are Prompting Many Americans to Stock Up on Long-Term Storage Beef It’s becoming increasingly clear that fiat currencies across the globe, including the U.S. Dollar, are under attack. Paper money is losing its value, translating into insane inflation and less value in our life’s savings. Genesis Gold Group believes physical precious metals are an amazing option for those seeking to move their wealth or retirement to higher ground. Whether Central Bank Digital Currencies replace current fiat currencies or not, precious metals are poised to retain or even increase in value. This is why central banks and mega-asset managers like BlackRock are moving much of their holdings to precious metals. As a Christian company, Genesis Gold Group has maintained a perfect 5 out of 5 rating with the Better Business Bureau. Their faith-driven values allow them to help Americans protect their life’s savings without the gimmicks used by most precious metals companies. Reach out to them today to see how they can streamline the rollover or transfer of your current and previous retirement accounts. https://discernreport.com/air-vax-the-latest-mrna-delivered-into-lungs/
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  • Paul Serran - Nova-C Lunar Mission Takes off in Florida, on Its Way to the First American Moon Landing in More Than Half a Century:

    https://www.thegatewaypundit.com/2024/02/space-odissey-nova-c-lunar-mission-takes-florida/

    #Odysseus #LunarLander #NovaC #IntuitiveMachines #IM1 #NASA #MalapertA #SolarSystemScience #Astronomy
    Paul Serran - Nova-C Lunar Mission Takes off in Florida, on Its Way to the First American Moon Landing in More Than Half a Century: https://www.thegatewaypundit.com/2024/02/space-odissey-nova-c-lunar-mission-takes-florida/ #Odysseus #LunarLander #NovaC #IntuitiveMachines #IM1 #NASA #MalapertA #SolarSystemScience #Astronomy
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  • FRIGHTENING TRUTH: Airborne mRNA Vaccines are being created that can be delivered straight into the Lungs without the need for Injection
    The ExposéDecember 22, 2023
    Researchers have developed an airborne mRNA vaccine offering a vehicle by which to rapidly vaccinate the masses without their knowledge or consent.

    A team from Yale University has developed a new airborne method for delivering mRNA right to your lungs. The method has also been used to vaccinate mice intranasally, “opening the door for human testing in the near future.”

    While scientists may celebrate this invention as a convenient method to vaccinate large populations, skeptics raise obvious concerns about the potential misuse of an airborne vaccine, including the possibility of covert bioenhancements a concept that has previously been suggested in academic literature. (source).

    Let’s not lose touch…Your Government and Big Tech are actively trying to censor the information reported by The Exposé to serve their own needs. Subscribe now to make sure you receive the latest uncensored news in your inbox…

    Roman Balmakov of Facts Matter discusses the study in the video below

    The Study: Polymer nanoparticles deliver mRNA to the lung for mucosal vaccination

    In a research conducted on mice, scientists from Yale University developed polymer nanoparticles to encapsulate mRNA, transforming it into an inhalable form for delivery to the lungs. Courtney Malo, who serves as an editor at Science Translational Medicine, the publication that featured the study, explained,

    “The ability to efficiently deliver mRNA to the lung would have applications for vaccine development, gene therapy, and more. Here, Suberi et al. showed that such mRNA delivery can be accomplished by encapsulating mRNAs of interest within optimized poly(amine-co-ester) polyplexes [nanoparticles].

    Polyplex-delivered mRNAs were efficiently translated into protein in the lungs of mice with limited evidence of toxicity. This platform was successfully applied as an intranasal SARS-CoV-2 vaccine, eliciting robust immune responses that conferred protection against subsequent viral challenge.

    These results highlight the potential of this delivery system for vaccine applications and beyond.“

    The team, which was led by cellular and molecular physiologist Mark Saltzman, claims that the inhalable mRNA vaccine “successfully protected against “SARS-CoV-2“, and that it “opens the door to delivering other messenger RNA (mRNA) therapeutics for gene replacement therapy and other treatments in the lungs.”(source)


    For the study, mice received two intranasal doses of nanoparticles carrying mRNA COVID-19 vaccines, which proved to be effective in the animals. In the past, lung-targeted mRNA therapies had trouble making it into the cells necessary to express the encoded protein, known as poor transfection efficiency (source).

    “The Saltzman group got around this hurdle in part by using a nanoparticle made from poly(amine-co-ester) polyplexes, or PACE, a biocompatible and highly customizable polymer,” a Yale University news release explained. In a previous study, Saltzman had tried a “prime and spike” system to deliver COVID-19 shots, which involved injecting mRNA shots into a muscle, then spraying spike proteins into the nose.

    It turned out the injection portion may be unnecessary, and Saltzman has high hopes for the airborne delivery method, beyond vaccines: (source).

    “In the new report, there is no intramuscular injection. We just gave two doses, a prime, and a boost, intranasally, and we got a highly protective immune response. But we also showed that, generally, you can deliver different kinds of mRNA. So it’s not just good for a vaccine, but potentially also good for gene replacement therapy in diseases like cystic fibrosis and gene editing.

    We used a vaccine example to show that it works, but it opens the door to doing all these other kinds of interventions.”

    Air Vax Could ‘Radically Change’ How People Are Vaccinated

    Saltzman says this “new method of delivery could ‘radically change the way people are vaccinated,’” making it easier to vaccinate people in remote areas or those who are afraid of needles.10 But that’s not all. An airborne vaccine makes it possible to rapidly disseminate it across a population.

    No Jab Needed

    By releasing the vaccine in the air, there’s no need to inject each person individually — which is not only time-consuming but difficult if an individual objects to the shot. This isn’t the case with an airborne vaccine, which can be released into the air without consent or even the public’s knowledge.

    A similar strategy is being used with mRNA in shrimp, which are too small and numerous to be injected individually. Instead, an oral “nanovaccine” was created to stop the spread of a virus. Shai Ufaz, chief executive officer of ViAqua, which developed the technology, stated:

    “Oral delivery is the holy grail of aquaculture health development due to both the impossibility of vaccinating individual shrimp and its ability to substantially bring down the operational costs of disease management while improving outcomes …”

    While the Yale scientists are targeting an intranasal mRNA product, the outcome is the same — get as many exposed as possible with the least amount of cost and effort. According to the Yale study:

    “An inhalable platform for messenger RNA (mRNA) therapeutics would enable minimally invasive and lung-targeted delivery for a host of pulmonary diseases. Development of lung-targeted mRNA therapeutics has been limited by poor transfection efficiency and risk of vehicle-induced pathology.

    Here, we report an inhalable polymer-based vehicle for the delivery of therapeutic mRNAs to the lung. We optimized biodegradable poly(amine-co-ester) (PACE) polyplexes [nanoparticles] for mRNA delivery using end-group modifications and polyethylene glycol. These polyplexes achieved high transfection of mRNA throughout the lung, particularly in epithelial and antigen-presenting cells.

    We applied this technology to develop a mucosal vaccine for severe acute respiratory syndrome coronavirus 2 and found that intranasal vaccination with spike protein–encoding mRNA polyplexes induced potent cellular and humoral adaptive immunity and protected susceptible mice from lethal viral challenge. Together, these results demonstrate the translational potential of PACE polyplexes for therapeutic delivery of mRNA to the lungs.”

    The following excerpts are from Dr Joseph Mercola, who explains his concerns regarding the airborne mRNA

    US Government Has History of Bioweapons Release

    When you put the pieces of the puzzle together, a disturbing picture emerges. As reported by The Epoch Times, we have a history of the U.S. government taking extreme measures to mandate and promote COVID-19 shots to the public. Now, researchers have developed an airborne mRNA vaccine, offering a vehicle by which to rapidly vaccinate the masses without their knowledge or consent (source).

    Is there proof that the government or another entity has plans to covertly release an air vax on the population? No. But there is a history of it carrying out secret bioweapon simulations on Americans. In 1950, the U.S. Navy sprayed Serratia marcescens bacteria into the air near San Francisco over a period of six days.

    Dubbed “Operation Sea Spray,” the project was intended to determine how susceptible the city was to a bioweapon attack. Serratia marcescens turns whatever it touches bright red, making it easy to track. It spread throughout the city, as residents inhaled the microbes from the air. While the U.S. military initially thought Serratia marcescens wouldn’t harm humans, an outbreak occurred, with some developing urinary tract infections as a result.

    At least one person died “and some have suggested that the release forever changed the area’s microbial ecology,” Smithsonian Magazine reported. This wasn’t an isolated incident, as the U.S. government carried out many other experiments across the U.S. over the next 20 years. (source).

    So, while it’s disturbing to think of an air vax experiment being conducted on an unsuspecting public, it’s not unprecedented.

    Bioethics Study Promotes Covert, Compulsory Bioenhancement

    Adding to the story is academic endorsement of the use of compulsory, covert bioenhancements. Writing in the journal Bioethics, Parker Crutchfield with Western Michigan University, Homer Stryker M.D. School of Medicine, discusses moral bioenhancements, which refers to the use of biomedical means to trigger moral improvements.

    Drug treatments, including vaccines, and genetic engineering are potential examples of bioenhancements. Further, according to Crutchfield:

    “It is necessary to morally bioenhance the population in order to prevent ultimate harm. Moral bioenhancement is the potential practice of influencing a person’s moral behavior by way of biological intervention upon their moral attitudes, motivations, or dispositions.

    The technology that may permit moral bioenhancement is on the scale between nonexistent and nascent, but common examples of potential interventions include infusing water supplies with pharmaceuticals that enhance empathy or altruism or otherwise intervening on a person’s emotions or motivations, in an attempt to influence the person’s moral behavior.”

    Some argue that moral bioenhancements should be compulsory for the greater good. Crutchfield believes this doesn’t go far enough. He also wants them to be covert: (source).

    “I take this argument one step further, arguing that if moral bioenhancement ought to be compulsory, then its administration ought to be covert rather than overt. This is to say that it is morally preferable for compulsory moral bioenhancement to be administered without the recipients knowing that they are receiving the enhancement.”

    He even goes so far as to suggest “a covert compulsory program promotes values such as liberty, utility, equality and autonomy better than an overt program does.” (source).

    So here we have evidence of academic support for covertly releasing drugs and other bioenhancements onto the public. This, combined with the creation of an airborne mRNA vaccine and the government’s history of experimenting on the public, paints an unsettling picture of the future.

    Problems With mRNA COVID Shots Persist

    Aside from the concerns of airborne delivery, mRNA COVID-19 shots are associated with significant risks — no matter how you’re exposed. People ages 65 and older who received Pfizer’s updated (bivalent) COVID-19 booster shot may be at increased risk of stroke, according to an announcement made by the U.S. Centers for Disease Control and Prevention and the Food and Drug Administration. (source).

    Further, a large study from Israel revealed that Pfizer’s COVID-19 mRNA jab is associated with a threefold increased risk of myocarditis, leading to the condition at a rate of 1 to 5 events per 100,000 persons (source). Other elevated risks were also identified following the COVID jab, including lymphadenopathy (swollen lymph nodes), appendicitis, and herpes zoster infection (source).

    At least 16,183 people also say they’ve developed tinnitus after receiving a COVID-19 shot (source). The reports were filed with the CDC’s Vaccine Adverse Event Reporting System (VAERS) database. But considering only between 1% and 10% of adverse reactions are ever reported to VAERS, the actual number is likely much higher.

    It’s because of risks like these that informed consent is essential for any medical procedure, including vaccinations. The development of airborne mRNA jabs, however, makes the possibility of informed consent being taken away all the more real. From Mercola


    FRIGHTENING TRUTH: Airborne mRNA Vaccines are being created that can be delivered straight into the Lungs without the need for Injection

    https://expose-news.com/2023/12/22/airborne-mrna-vaccines-are-being-created

    T.me/AgentsOfTruth
    T.me/AgentsOfTruthChat
    FRIGHTENING TRUTH: Airborne mRNA Vaccines are being created that can be delivered straight into the Lungs without the need for Injection The ExposéDecember 22, 2023 Researchers have developed an airborne mRNA vaccine offering a vehicle by which to rapidly vaccinate the masses without their knowledge or consent. A team from Yale University has developed a new airborne method for delivering mRNA right to your lungs. The method has also been used to vaccinate mice intranasally, “opening the door for human testing in the near future.” While scientists may celebrate this invention as a convenient method to vaccinate large populations, skeptics raise obvious concerns about the potential misuse of an airborne vaccine, including the possibility of covert bioenhancements a concept that has previously been suggested in academic literature. (source). Let’s not lose touch…Your Government and Big Tech are actively trying to censor the information reported by The Exposé to serve their own needs. Subscribe now to make sure you receive the latest uncensored news in your inbox… Roman Balmakov of Facts Matter discusses the study in the video below The Study: Polymer nanoparticles deliver mRNA to the lung for mucosal vaccination In a research conducted on mice, scientists from Yale University developed polymer nanoparticles to encapsulate mRNA, transforming it into an inhalable form for delivery to the lungs. Courtney Malo, who serves as an editor at Science Translational Medicine, the publication that featured the study, explained, “The ability to efficiently deliver mRNA to the lung would have applications for vaccine development, gene therapy, and more. Here, Suberi et al. showed that such mRNA delivery can be accomplished by encapsulating mRNAs of interest within optimized poly(amine-co-ester) polyplexes [nanoparticles]. Polyplex-delivered mRNAs were efficiently translated into protein in the lungs of mice with limited evidence of toxicity. This platform was successfully applied as an intranasal SARS-CoV-2 vaccine, eliciting robust immune responses that conferred protection against subsequent viral challenge. These results highlight the potential of this delivery system for vaccine applications and beyond.“ The team, which was led by cellular and molecular physiologist Mark Saltzman, claims that the inhalable mRNA vaccine “successfully protected against “SARS-CoV-2“, and that it “opens the door to delivering other messenger RNA (mRNA) therapeutics for gene replacement therapy and other treatments in the lungs.”(source) For the study, mice received two intranasal doses of nanoparticles carrying mRNA COVID-19 vaccines, which proved to be effective in the animals. In the past, lung-targeted mRNA therapies had trouble making it into the cells necessary to express the encoded protein, known as poor transfection efficiency (source). “The Saltzman group got around this hurdle in part by using a nanoparticle made from poly(amine-co-ester) polyplexes, or PACE, a biocompatible and highly customizable polymer,” a Yale University news release explained. In a previous study, Saltzman had tried a “prime and spike” system to deliver COVID-19 shots, which involved injecting mRNA shots into a muscle, then spraying spike proteins into the nose. It turned out the injection portion may be unnecessary, and Saltzman has high hopes for the airborne delivery method, beyond vaccines: (source). “In the new report, there is no intramuscular injection. We just gave two doses, a prime, and a boost, intranasally, and we got a highly protective immune response. But we also showed that, generally, you can deliver different kinds of mRNA. So it’s not just good for a vaccine, but potentially also good for gene replacement therapy in diseases like cystic fibrosis and gene editing. We used a vaccine example to show that it works, but it opens the door to doing all these other kinds of interventions.” Air Vax Could ‘Radically Change’ How People Are Vaccinated Saltzman says this “new method of delivery could ‘radically change the way people are vaccinated,’” making it easier to vaccinate people in remote areas or those who are afraid of needles.10 But that’s not all. An airborne vaccine makes it possible to rapidly disseminate it across a population. No Jab Needed By releasing the vaccine in the air, there’s no need to inject each person individually — which is not only time-consuming but difficult if an individual objects to the shot. This isn’t the case with an airborne vaccine, which can be released into the air without consent or even the public’s knowledge. A similar strategy is being used with mRNA in shrimp, which are too small and numerous to be injected individually. Instead, an oral “nanovaccine” was created to stop the spread of a virus. Shai Ufaz, chief executive officer of ViAqua, which developed the technology, stated: “Oral delivery is the holy grail of aquaculture health development due to both the impossibility of vaccinating individual shrimp and its ability to substantially bring down the operational costs of disease management while improving outcomes …” While the Yale scientists are targeting an intranasal mRNA product, the outcome is the same — get as many exposed as possible with the least amount of cost and effort. According to the Yale study: “An inhalable platform for messenger RNA (mRNA) therapeutics would enable minimally invasive and lung-targeted delivery for a host of pulmonary diseases. Development of lung-targeted mRNA therapeutics has been limited by poor transfection efficiency and risk of vehicle-induced pathology. Here, we report an inhalable polymer-based vehicle for the delivery of therapeutic mRNAs to the lung. We optimized biodegradable poly(amine-co-ester) (PACE) polyplexes [nanoparticles] for mRNA delivery using end-group modifications and polyethylene glycol. These polyplexes achieved high transfection of mRNA throughout the lung, particularly in epithelial and antigen-presenting cells. We applied this technology to develop a mucosal vaccine for severe acute respiratory syndrome coronavirus 2 and found that intranasal vaccination with spike protein–encoding mRNA polyplexes induced potent cellular and humoral adaptive immunity and protected susceptible mice from lethal viral challenge. Together, these results demonstrate the translational potential of PACE polyplexes for therapeutic delivery of mRNA to the lungs.” The following excerpts are from Dr Joseph Mercola, who explains his concerns regarding the airborne mRNA US Government Has History of Bioweapons Release When you put the pieces of the puzzle together, a disturbing picture emerges. As reported by The Epoch Times, we have a history of the U.S. government taking extreme measures to mandate and promote COVID-19 shots to the public. Now, researchers have developed an airborne mRNA vaccine, offering a vehicle by which to rapidly vaccinate the masses without their knowledge or consent (source). Is there proof that the government or another entity has plans to covertly release an air vax on the population? No. But there is a history of it carrying out secret bioweapon simulations on Americans. In 1950, the U.S. Navy sprayed Serratia marcescens bacteria into the air near San Francisco over a period of six days. Dubbed “Operation Sea Spray,” the project was intended to determine how susceptible the city was to a bioweapon attack. Serratia marcescens turns whatever it touches bright red, making it easy to track. It spread throughout the city, as residents inhaled the microbes from the air. While the U.S. military initially thought Serratia marcescens wouldn’t harm humans, an outbreak occurred, with some developing urinary tract infections as a result. At least one person died “and some have suggested that the release forever changed the area’s microbial ecology,” Smithsonian Magazine reported. This wasn’t an isolated incident, as the U.S. government carried out many other experiments across the U.S. over the next 20 years. (source). So, while it’s disturbing to think of an air vax experiment being conducted on an unsuspecting public, it’s not unprecedented. Bioethics Study Promotes Covert, Compulsory Bioenhancement Adding to the story is academic endorsement of the use of compulsory, covert bioenhancements. Writing in the journal Bioethics, Parker Crutchfield with Western Michigan University, Homer Stryker M.D. School of Medicine, discusses moral bioenhancements, which refers to the use of biomedical means to trigger moral improvements. Drug treatments, including vaccines, and genetic engineering are potential examples of bioenhancements. Further, according to Crutchfield: “It is necessary to morally bioenhance the population in order to prevent ultimate harm. Moral bioenhancement is the potential practice of influencing a person’s moral behavior by way of biological intervention upon their moral attitudes, motivations, or dispositions. The technology that may permit moral bioenhancement is on the scale between nonexistent and nascent, but common examples of potential interventions include infusing water supplies with pharmaceuticals that enhance empathy or altruism or otherwise intervening on a person’s emotions or motivations, in an attempt to influence the person’s moral behavior.” Some argue that moral bioenhancements should be compulsory for the greater good. Crutchfield believes this doesn’t go far enough. He also wants them to be covert: (source). “I take this argument one step further, arguing that if moral bioenhancement ought to be compulsory, then its administration ought to be covert rather than overt. This is to say that it is morally preferable for compulsory moral bioenhancement to be administered without the recipients knowing that they are receiving the enhancement.” He even goes so far as to suggest “a covert compulsory program promotes values such as liberty, utility, equality and autonomy better than an overt program does.” (source). So here we have evidence of academic support for covertly releasing drugs and other bioenhancements onto the public. This, combined with the creation of an airborne mRNA vaccine and the government’s history of experimenting on the public, paints an unsettling picture of the future. Problems With mRNA COVID Shots Persist Aside from the concerns of airborne delivery, mRNA COVID-19 shots are associated with significant risks — no matter how you’re exposed. People ages 65 and older who received Pfizer’s updated (bivalent) COVID-19 booster shot may be at increased risk of stroke, according to an announcement made by the U.S. Centers for Disease Control and Prevention and the Food and Drug Administration. (source). Further, a large study from Israel revealed that Pfizer’s COVID-19 mRNA jab is associated with a threefold increased risk of myocarditis, leading to the condition at a rate of 1 to 5 events per 100,000 persons (source). Other elevated risks were also identified following the COVID jab, including lymphadenopathy (swollen lymph nodes), appendicitis, and herpes zoster infection (source). At least 16,183 people also say they’ve developed tinnitus after receiving a COVID-19 shot (source). The reports were filed with the CDC’s Vaccine Adverse Event Reporting System (VAERS) database. But considering only between 1% and 10% of adverse reactions are ever reported to VAERS, the actual number is likely much higher. It’s because of risks like these that informed consent is essential for any medical procedure, including vaccinations. The development of airborne mRNA jabs, however, makes the possibility of informed consent being taken away all the more real. From Mercola FRIGHTENING TRUTH: Airborne mRNA Vaccines are being created that can be delivered straight into the Lungs without the need for Injection https://expose-news.com/2023/12/22/airborne-mrna-vaccines-are-being-created T.me/AgentsOfTruth T.me/AgentsOfTruthChat
    EXPOSE-NEWS.COM
    FRIGHTENING TRUTH: Airborne mRNA Vaccines are being created that can be delivered straight into the Lungs without the need for Injection
    Researchers have developed an airborne mRNA vaccine offering a vehicle by which to rapidly vaccinate the masses without their knowledge or consent. A team from Yale University has developed a new a…
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  • My Story - By Professor Gabriel Oon
    "Between 2021 and now, I have lost 34 senior medical colleagues. Most were working in institutions and had been vaccinated with Pfizer."

    Aussie17
    Dear Readers, today I bring to you a guest post by Professor Gabriel Oon, retired Professor of Medicine who worked as a WHO consultant and founding President of Singapore’s Society of Oncology. Please feel free to share and distribute!

    -Aussie17

    Share


    My Story - By Professor Gabriel Oon

    "SAFETY, SAFETY, SAFETY!"

    These words were relentlessly drummed upon us during our WHO meetings in Geneva from 1983 to 1987, where vaccine manufacturers from around the globe (Netherlands, Germany, China, Singapore, Korea, Australia, US, UK, France, Russia, Sweden, Israel, etc.) came together. The gathering was initiated by the Director of Biologics, Dr. Frank Perkins, and the Director-General, Dr. Karl Mahler MD, who had appointed me as a WHO Consultant.

    Every one of us had created our own variant of the novel hepatitis B vaccine from plasma HBV, employing different inactivation techniques.

    Dr. Perkins reminded us of the two monumental vaccine calamities in history.

    The Lübeck disaster (1929-33) saw many children inoculated with live BCG instead of the killed vaccine, resulting in thousands of children affected and several deaths.

    The Cutter incident (1955) in the USA was when 200,000 received a live polio vaccine; 40,000 fell ill, many became paralyzed, or died.

    Such tragedies were not to be repeated. With the then-unknown threat of AIDS transmitted by infected blood, it became crucial to source safe, uninfected blood for the production of hepatitis B vaccines.

    Advancements in molecular science led to the discovery of the common “a” antigen present in all serotypes in both humans and animals. Consequently, a prototype yeast recombinant HB vaccine was formulated, safety-tested, and implemented in Singapore as a collaboration between the International Agency for Research in Cancer/WHO and the Singapore Government.

    I was then appointed by the Singapore government and IARC/WHO (International Agency for Research on Cancer) to oversee the safety in the manufacture and implementation of the vaccine.

    Then Prime Minister of Singapore, Mr. Lee Kuan Yew, who mandated the directive to me and my team, insisted on "300% safety, not just 100%."

    Together with my team and WHO oversight, we rejected several unsafe vaccines and identified vaccine-escape mutants in plasma vaccines that were over-treated with chemicals, which damaged the epitopes of the “a” antigen. This product was rejected.

    Similar Vaccine Escape Mutants (VEMs) arose with the Pfizer mRNA. Instead of inactivation, nine chemicals were used, including the deep-freezing agent phosphophenolglycol. I believe these VEMs on the Covid mRNA are the cause of the continuous eruption of spike mutants ranging from Delta to Omicron variants seen today, as humans have become reservoirs for these mutants.

    On my 80th birthday, July 4, 2019, 34 years since the WHO consultation, I announced the complete elimination of HBV and associated lethal liver failures and liver cancer at a Duke-NUS lecture (video below).

    SARS-2/COVID-19

    In October 2018, my wife and I returned from a Yangtze River Cruise where we had admired the beautiful and ancient industrial city of Wuhan, home to 8 million people.

    START OF THE COVID PANDEMIC: January 2020

    We woke to the news that Wuhan was besieged by a lethal coronavirus, resulting in thousands dead daily and several more thousands hospitalized until hospitals reached full capacity. Field hospitals were erected within days. Doctors and nurses arrived from all over China to provide aid; tragically, around a thousand of them died.

    Within a week, top Chinese scientists had determined the molecular structure of the coronavirus, which was dissimilar to any of the known viruses in their archives.

    The molecular structure seemed akin to the USCDC's patented invention (No. 7220852/B1 filed on May 22, 2004), with the addition of an HIV glycoprotein insert in the spike protein (later confirmed by Nobel Laureate Prof. Luc Montagnier).

    China disseminated information on the epidemic and the virus through premier journals and transmitted details to the International Genomic Bank. They invited the WHO in January 2020, who discovered many corona viruses but not this particular virus.

    Singapore

    We learned from the news that SG Prime Minister's wife, Ho Ching, chairman of Temasek Holdings, a Singapore investment company, had invested nearly S$3 billion in Pfizer/BioNTech and had initiated the procurement of Pfizer mRNA vaccines, Moderna, and plans for establishing vaccine manufacturing in Singapore.

    Pfizer and mRNA Vaccines

    Publications in JAMA 2021 showed that Pfizer was 98% effective. Six of my senior academic staff on the board of journals agreed with me that the end points for assessing efficacy were symptoms.

    (Later, a US Texas judge in 2022 ordered the FDA to release 55,000 pages showing thousands of deaths and serious adverse reactions. The US Supreme Court in 2022 also accepted Senator Robert Kennedy's charge that mRNA vaccines are not vaccines.)

    These were not the usual endpoints like antibody levels and virus absence in recipients. This was open to "ghost papers," which we had discovered at WHO.

    I alerted our three Ministers who know me and the 14 medical experts, "The Pfizer mRNA vaccines are not safe for mass immunization as the live lethal virus is still present in the mRNAs."

    Mandatory Vaccination

    Then, we received notice from our MOH (Ministry of Health) that all hospital and clinic staff, workplaces, and schools must be vaccinated or they cannot work.

    Retirement

    I was then 82 years old, and my mission after being recalled/returning from Cambridge with an MD in Cancer Immunology was completed. However, with my vast experience with vaccines, I continued to advise our MOH privately, as well as colleagues and friends in our country and worldwide.

    Request to MOH to Release Sinovac

    A full-length inactivated COVID virus vaccine, Singapore had 20,000 doses of Sinovac in stock. When the new Delta variant infected frontline workers in five public hospitals and Changi Airport in May 2021, I advised our Ministers that the mRNA vaccines were not preventative and to use Sinovac lest our hospitals be overwhelmed by infections.

    I also informed Ministers that many individuals with allergies cannot take mRNA vaccines and to release the Sinovac.

    This news was leaked, and I was chastised as peddling fake news by Prof. David Lye of the National Infectious Disease Center and senior Straits Times journalist Shamir Khalid.

    The Future

    COVID will remain for many years as the reservoirs of VEMs (Vaccine Escape Mutates) are evolving from failed protection in millions but causing deaths, delayed deaths, and illnesses.

    The 95% who received Pfizer and other mRNA vaccines, and not inactivated vaccines like Novavax, are developing new mutants.

    Losses

    Between 2021 and now, I have lost 34 senior medical colleagues. Most were working in institutions and had been vaccinated with Pfizer.

    I lost my eminent elder obstetrician aunt on March 31, 2022, who was infected by a Pfizer-vaccinated caregiver who had contracted the Delta spike mutant. She became too weak, stopped playing mahjong, stopped eating, and five days before she passed, she became blind. She died in my arms.

    I also lost my elder brother, a senior physician at 85, who received Moderna followed by two boosters of Pfizer. He contracted COVID and died two months later.

    How to Eliminate

    Wear masks to reduce aerosol transmission.

    Use antiviral drugs like Tamiflu, 75mg daily for 7 days. It is a potent neuraminidase inhibitor of COVID and the flu. As with most serious infections, take it early at the onset. Usually, ART is negative on day 2-3.

    Vaccine Research - With the many combinations of mutations, we need to find common antigens and make new inactivated vaccines.

    Sinovac and Sinopharm

    My wife and I have had three doses of Sinovac and two of Sinopharm. We have nucleocapsid spike antibodies and are well.

    1.6 billion people, including children in 150 countries, have taken the Sinovac and Sinopharm vaccines. They are safe, protective, and have caused no fatalities. Countries can copy or learn from China. Save lives, not politics first.

    Retired, we stay at home and wear masks in crowded areas.

    Lessons

    It's essential to control and eliminate lethal airborne/aerosol infections.
    A healthy population is a robust workforce.
    A healthy youth is the future of our country.

    God bless all,
    Gabriel Oon
    Retired Professor of Medicine
    Former WHO Consultant for Biologicals for Human Use


    Some final comments by Aussie17:
    I am fully aware that there are people who are against any kind of vaccine, people who are against wearing masks, and people who believe there is no such thing as viruses. Whatever your opinion is on these matters, I’d just like to say that I know Professor Gabriel personally, and he does not have a single nefarious bone in his body. The world is such a divided place right now that even when you agree with someone 99%, people start calling names and scolding each other over the 1% disagreement, which only serves to deepen our divisions. I hope we can accept diverse views and come together.

    Signing off for now
    A17

    Thank you for reading PharmaFiles by Aussie17. This post is public so feel free to share it.

    Share

    https://www.aussie17.com/p/my-story-by-professor-gabriel-oon
    My Story - By Professor Gabriel Oon "Between 2021 and now, I have lost 34 senior medical colleagues. Most were working in institutions and had been vaccinated with Pfizer." Aussie17 Dear Readers, today I bring to you a guest post by Professor Gabriel Oon, retired Professor of Medicine who worked as a WHO consultant and founding President of Singapore’s Society of Oncology. Please feel free to share and distribute! -Aussie17 Share My Story - By Professor Gabriel Oon "SAFETY, SAFETY, SAFETY!" These words were relentlessly drummed upon us during our WHO meetings in Geneva from 1983 to 1987, where vaccine manufacturers from around the globe (Netherlands, Germany, China, Singapore, Korea, Australia, US, UK, France, Russia, Sweden, Israel, etc.) came together. The gathering was initiated by the Director of Biologics, Dr. Frank Perkins, and the Director-General, Dr. Karl Mahler MD, who had appointed me as a WHO Consultant. Every one of us had created our own variant of the novel hepatitis B vaccine from plasma HBV, employing different inactivation techniques. Dr. Perkins reminded us of the two monumental vaccine calamities in history. The Lübeck disaster (1929-33) saw many children inoculated with live BCG instead of the killed vaccine, resulting in thousands of children affected and several deaths. The Cutter incident (1955) in the USA was when 200,000 received a live polio vaccine; 40,000 fell ill, many became paralyzed, or died. Such tragedies were not to be repeated. With the then-unknown threat of AIDS transmitted by infected blood, it became crucial to source safe, uninfected blood for the production of hepatitis B vaccines. Advancements in molecular science led to the discovery of the common “a” antigen present in all serotypes in both humans and animals. Consequently, a prototype yeast recombinant HB vaccine was formulated, safety-tested, and implemented in Singapore as a collaboration between the International Agency for Research in Cancer/WHO and the Singapore Government. I was then appointed by the Singapore government and IARC/WHO (International Agency for Research on Cancer) to oversee the safety in the manufacture and implementation of the vaccine. Then Prime Minister of Singapore, Mr. Lee Kuan Yew, who mandated the directive to me and my team, insisted on "300% safety, not just 100%." Together with my team and WHO oversight, we rejected several unsafe vaccines and identified vaccine-escape mutants in plasma vaccines that were over-treated with chemicals, which damaged the epitopes of the “a” antigen. This product was rejected. Similar Vaccine Escape Mutants (VEMs) arose with the Pfizer mRNA. Instead of inactivation, nine chemicals were used, including the deep-freezing agent phosphophenolglycol. I believe these VEMs on the Covid mRNA are the cause of the continuous eruption of spike mutants ranging from Delta to Omicron variants seen today, as humans have become reservoirs for these mutants. On my 80th birthday, July 4, 2019, 34 years since the WHO consultation, I announced the complete elimination of HBV and associated lethal liver failures and liver cancer at a Duke-NUS lecture (video below). SARS-2/COVID-19 In October 2018, my wife and I returned from a Yangtze River Cruise where we had admired the beautiful and ancient industrial city of Wuhan, home to 8 million people. START OF THE COVID PANDEMIC: January 2020 We woke to the news that Wuhan was besieged by a lethal coronavirus, resulting in thousands dead daily and several more thousands hospitalized until hospitals reached full capacity. Field hospitals were erected within days. Doctors and nurses arrived from all over China to provide aid; tragically, around a thousand of them died. Within a week, top Chinese scientists had determined the molecular structure of the coronavirus, which was dissimilar to any of the known viruses in their archives. The molecular structure seemed akin to the USCDC's patented invention (No. 7220852/B1 filed on May 22, 2004), with the addition of an HIV glycoprotein insert in the spike protein (later confirmed by Nobel Laureate Prof. Luc Montagnier). China disseminated information on the epidemic and the virus through premier journals and transmitted details to the International Genomic Bank. They invited the WHO in January 2020, who discovered many corona viruses but not this particular virus. Singapore We learned from the news that SG Prime Minister's wife, Ho Ching, chairman of Temasek Holdings, a Singapore investment company, had invested nearly S$3 billion in Pfizer/BioNTech and had initiated the procurement of Pfizer mRNA vaccines, Moderna, and plans for establishing vaccine manufacturing in Singapore. Pfizer and mRNA Vaccines Publications in JAMA 2021 showed that Pfizer was 98% effective. Six of my senior academic staff on the board of journals agreed with me that the end points for assessing efficacy were symptoms. (Later, a US Texas judge in 2022 ordered the FDA to release 55,000 pages showing thousands of deaths and serious adverse reactions. The US Supreme Court in 2022 also accepted Senator Robert Kennedy's charge that mRNA vaccines are not vaccines.) These were not the usual endpoints like antibody levels and virus absence in recipients. This was open to "ghost papers," which we had discovered at WHO. I alerted our three Ministers who know me and the 14 medical experts, "The Pfizer mRNA vaccines are not safe for mass immunization as the live lethal virus is still present in the mRNAs." Mandatory Vaccination Then, we received notice from our MOH (Ministry of Health) that all hospital and clinic staff, workplaces, and schools must be vaccinated or they cannot work. Retirement I was then 82 years old, and my mission after being recalled/returning from Cambridge with an MD in Cancer Immunology was completed. However, with my vast experience with vaccines, I continued to advise our MOH privately, as well as colleagues and friends in our country and worldwide. Request to MOH to Release Sinovac A full-length inactivated COVID virus vaccine, Singapore had 20,000 doses of Sinovac in stock. When the new Delta variant infected frontline workers in five public hospitals and Changi Airport in May 2021, I advised our Ministers that the mRNA vaccines were not preventative and to use Sinovac lest our hospitals be overwhelmed by infections. I also informed Ministers that many individuals with allergies cannot take mRNA vaccines and to release the Sinovac. This news was leaked, and I was chastised as peddling fake news by Prof. David Lye of the National Infectious Disease Center and senior Straits Times journalist Shamir Khalid. The Future COVID will remain for many years as the reservoirs of VEMs (Vaccine Escape Mutates) are evolving from failed protection in millions but causing deaths, delayed deaths, and illnesses. The 95% who received Pfizer and other mRNA vaccines, and not inactivated vaccines like Novavax, are developing new mutants. Losses Between 2021 and now, I have lost 34 senior medical colleagues. Most were working in institutions and had been vaccinated with Pfizer. I lost my eminent elder obstetrician aunt on March 31, 2022, who was infected by a Pfizer-vaccinated caregiver who had contracted the Delta spike mutant. She became too weak, stopped playing mahjong, stopped eating, and five days before she passed, she became blind. She died in my arms. I also lost my elder brother, a senior physician at 85, who received Moderna followed by two boosters of Pfizer. He contracted COVID and died two months later. How to Eliminate Wear masks to reduce aerosol transmission. Use antiviral drugs like Tamiflu, 75mg daily for 7 days. It is a potent neuraminidase inhibitor of COVID and the flu. As with most serious infections, take it early at the onset. Usually, ART is negative on day 2-3. Vaccine Research - With the many combinations of mutations, we need to find common antigens and make new inactivated vaccines. Sinovac and Sinopharm My wife and I have had three doses of Sinovac and two of Sinopharm. We have nucleocapsid spike antibodies and are well. 1.6 billion people, including children in 150 countries, have taken the Sinovac and Sinopharm vaccines. They are safe, protective, and have caused no fatalities. Countries can copy or learn from China. Save lives, not politics first. Retired, we stay at home and wear masks in crowded areas. Lessons It's essential to control and eliminate lethal airborne/aerosol infections. A healthy population is a robust workforce. A healthy youth is the future of our country. God bless all, Gabriel Oon Retired Professor of Medicine Former WHO Consultant for Biologicals for Human Use Some final comments by Aussie17: I am fully aware that there are people who are against any kind of vaccine, people who are against wearing masks, and people who believe there is no such thing as viruses. Whatever your opinion is on these matters, I’d just like to say that I know Professor Gabriel personally, and he does not have a single nefarious bone in his body. The world is such a divided place right now that even when you agree with someone 99%, people start calling names and scolding each other over the 1% disagreement, which only serves to deepen our divisions. I hope we can accept diverse views and come together. Signing off for now A17 Thank you for reading PharmaFiles by Aussie17. This post is public so feel free to share it. Share https://www.aussie17.com/p/my-story-by-professor-gabriel-oon
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    My Story - By Professor Gabriel Oon
    "Between 2021 and now, I have lost 34 senior medical colleagues. Most were working in institutions and had been vaccinated with Pfizer."
    Angry
    1
    0 Comments 1 Shares 14780 Views
  • My Story - By Professor Gabriel Oon
    "Between 2021 and now, I have lost 34 senior medical colleagues. Most were working in institutions and had been vaccinated with Pfizer."

    Aussie17
    Dear Readers, today I bring to you a guest post by Professor Gabriel Oon, retired Professor of Medicine who worked as a WHO consultant and founding President of Singapore’s Society of Oncology. Please feel free to share and distribute!

    -Aussie17

    Share


    My Story - By Professor Gabriel Oon

    "SAFETY, SAFETY, SAFETY!"

    These words were relentlessly drummed upon us during our WHO meetings in Geneva from 1983 to 1987, where vaccine manufacturers from around the globe (Netherlands, Germany, China, Singapore, Korea, Australia, US, UK, France, Russia, Sweden, Israel, etc.) came together. The gathering was initiated by the Director of Biologics, Dr. Frank Perkins, and the Director-General, Dr. Karl Mahler MD, who had appointed me as a WHO Consultant.

    Every one of us had created our own variant of the novel hepatitis B vaccine from plasma HBV, employing different inactivation techniques.

    Dr. Perkins reminded us of the two monumental vaccine calamities in history.

    The Lübeck disaster (1929-33) saw many children inoculated with live BCG instead of the killed vaccine, resulting in thousands of children affected and several deaths.

    The Cutter incident (1955) in the USA was when 200,000 received a live polio vaccine; 40,000 fell ill, many became paralyzed, or died.

    Such tragedies were not to be repeated. With the then-unknown threat of AIDS transmitted by infected blood, it became crucial to source safe, uninfected blood for the production of hepatitis B vaccines.

    Advancements in molecular science led to the discovery of the common “a” antigen present in all serotypes in both humans and animals. Consequently, a prototype yeast recombinant HB vaccine was formulated, safety-tested, and implemented in Singapore as a collaboration between the International Agency for Research in Cancer/WHO and the Singapore Government.

    I was then appointed by the Singapore government and IARC/WHO (International Agency for Research on Cancer) to oversee the safety in the manufacture and implementation of the vaccine.

    Then Prime Minister of Singapore, Mr. Lee Kuan Yew, who mandated the directive to me and my team, insisted on "300% safety, not just 100%."

    Together with my team and WHO oversight, we rejected several unsafe vaccines and identified vaccine-escape mutants in plasma vaccines that were over-treated with chemicals, which damaged the epitopes of the “a” antigen. This product was rejected.

    Similar Vaccine Escape Mutants (VEMs) arose with the Pfizer mRNA. Instead of inactivation, nine chemicals were used, including the deep-freezing agent phosphophenolglycol. I believe these VEMs on the Covid mRNA are the cause of the continuous eruption of spike mutants ranging from Delta to Omicron variants seen today, as humans have become reservoirs for these mutants.

    On my 80th birthday, July 4, 2019, 34 years since the WHO consultation, I announced the complete elimination of HBV and associated lethal liver failures and liver cancer at a Duke-NUS lecture (video below).

    SARS-2/COVID-19

    In October 2018, my wife and I returned from a Yangtze River Cruise where we had admired the beautiful and ancient industrial city of Wuhan, home to 8 million people.

    START OF THE COVID PANDEMIC: January 2020

    We woke to the news that Wuhan was besieged by a lethal coronavirus, resulting in thousands dead daily and several more thousands hospitalized until hospitals reached full capacity. Field hospitals were erected within days. Doctors and nurses arrived from all over China to provide aid; tragically, around a thousand of them died.

    Within a week, top Chinese scientists had determined the molecular structure of the coronavirus, which was dissimilar to any of the known viruses in their archives.

    The molecular structure seemed akin to the USCDC's patented invention (No. 7220852/B1 filed on May 22, 2004), with the addition of an HIV glycoprotein insert in the spike protein (later confirmed by Nobel Laureate Prof. Luc Montagnier).

    China disseminated information on the epidemic and the virus through premier journals and transmitted details to the International Genomic Bank. They invited the WHO in January 2020, who discovered many corona viruses but not this particular virus.

    Singapore

    We learned from the news that SG Prime Minister's wife, Ho Ching, chairman of Temasek Holdings, a Singapore investment company, had invested nearly S$3 billion in Pfizer/BioNTech and had initiated the procurement of Pfizer mRNA vaccines, Moderna, and plans for establishing vaccine manufacturing in Singapore.

    Pfizer and mRNA Vaccines

    Publications in JAMA 2021 showed that Pfizer was 98% effective. Six of my senior academic staff on the board of journals agreed with me that the end points for assessing efficacy were symptoms.

    (Later, a US Texas judge in 2022 ordered the FDA to release 55,000 pages showing thousands of deaths and serious adverse reactions. The US Supreme Court in 2022 also accepted Senator Robert Kennedy's charge that mRNA vaccines are not vaccines.)

    These were not the usual endpoints like antibody levels and virus absence in recipients. This was open to "ghost papers," which we had discovered at WHO.

    I alerted our three Ministers who know me and the 14 medical experts, "The Pfizer mRNA vaccines are not safe for mass immunization as the live lethal virus is still present in the mRNAs."

    Mandatory Vaccination

    Then, we received notice from our MOH (Ministry of Health) that all hospital and clinic staff, workplaces, and schools must be vaccinated or they cannot work.

    Retirement

    I was then 82 years old, and my mission after being recalled/returning from Cambridge with an MD in Cancer Immunology was completed. However, with my vast experience with vaccines, I continued to advise our MOH privately, as well as colleagues and friends in our country and worldwide.

    Request to MOH to Release Sinovac

    A full-length inactivated COVID virus vaccine, Singapore had 20,000 doses of Sinovac in stock. When the new Delta variant infected frontline workers in five public hospitals and Changi Airport in May 2021, I advised our Ministers that the mRNA vaccines were not preventative and to use Sinovac lest our hospitals be overwhelmed by infections.

    I also informed Ministers that many individuals with allergies cannot take mRNA vaccines and to release the Sinovac.

    This news was leaked, and I was chastised as peddling fake news by Prof. David Lye of the National Infectious Disease Center and senior Straits Times journalist Shamir Khalid.

    The Future

    COVID will remain for many years as the reservoirs of VEMs (Vaccine Escape Mutates) are evolving from failed protection in millions but causing deaths, delayed deaths, and illnesses.

    The 95% who received Pfizer and other mRNA vaccines, and not inactivated vaccines like Novavax, are developing new mutants.

    Losses

    Between 2021 and now, I have lost 34 senior medical colleagues. Most were working in institutions and had been vaccinated with Pfizer.

    I lost my eminent elder obstetrician aunt on March 31, 2022, who was infected by a Pfizer-vaccinated caregiver who had contracted the Delta spike mutant. She became too weak, stopped playing mahjong, stopped eating, and five days before she passed, she became blind. She died in my arms.

    I also lost my elder brother, a senior physician at 85, who received Moderna followed by two boosters of Pfizer. He contracted COVID and died two months later.

    How to Eliminate

    Wear masks to reduce aerosol transmission.

    Use antiviral drugs like Tamiflu, 75mg daily for 7 days. It is a potent neuraminidase inhibitor of COVID and the flu. As with most serious infections, take it early at the onset. Usually, ART is negative on day 2-3.

    Vaccine Research - With the many combinations of mutations, we need to find common antigens and make new inactivated vaccines.

    Sinovac and Sinopharm

    My wife and I have had three doses of Sinovac and two of Sinopharm. We have nucleocapsid spike antibodies and are well.

    1.6 billion people, including children in 150 countries, have taken the Sinovac and Sinopharm vaccines. They are safe, protective, and have caused no fatalities. Countries can copy or learn from China. Save lives, not politics first.

    Retired, we stay at home and wear masks in crowded areas.

    Lessons

    It's essential to control and eliminate lethal airborne/aerosol infections.
    A healthy population is a robust workforce.
    A healthy youth is the future of our country.

    God bless all,
    Gabriel Oon
    Retired Professor of Medicine
    Former WHO Consultant for Biologicals for Human Use


    Some final comments by Aussie17:
    I am fully aware that there are people who are against any kind of vaccine, people who are against wearing masks, and people who believe there is no such thing as viruses. Whatever your opinion is on these matters, I’d just like to say that I know Professor Gabriel personally, and he does not have a single nefarious bone in his body. The world is such a divided place right now that even when you agree with someone 99%, people start calling names and scolding each other over the 1% disagreement, which only serves to deepen our divisions. I hope we can accept diverse views and come together.

    Signing off for now
    A17

    Thank you for reading PharmaFiles by Aussie17. This post is public so feel free to share it.

    Share


    https://www.aussie17.com/p/my-story-by-professor-gabriel-oon
    My Story - By Professor Gabriel Oon "Between 2021 and now, I have lost 34 senior medical colleagues. Most were working in institutions and had been vaccinated with Pfizer." Aussie17 Dear Readers, today I bring to you a guest post by Professor Gabriel Oon, retired Professor of Medicine who worked as a WHO consultant and founding President of Singapore’s Society of Oncology. Please feel free to share and distribute! -Aussie17 Share My Story - By Professor Gabriel Oon "SAFETY, SAFETY, SAFETY!" These words were relentlessly drummed upon us during our WHO meetings in Geneva from 1983 to 1987, where vaccine manufacturers from around the globe (Netherlands, Germany, China, Singapore, Korea, Australia, US, UK, France, Russia, Sweden, Israel, etc.) came together. The gathering was initiated by the Director of Biologics, Dr. Frank Perkins, and the Director-General, Dr. Karl Mahler MD, who had appointed me as a WHO Consultant. Every one of us had created our own variant of the novel hepatitis B vaccine from plasma HBV, employing different inactivation techniques. Dr. Perkins reminded us of the two monumental vaccine calamities in history. The Lübeck disaster (1929-33) saw many children inoculated with live BCG instead of the killed vaccine, resulting in thousands of children affected and several deaths. The Cutter incident (1955) in the USA was when 200,000 received a live polio vaccine; 40,000 fell ill, many became paralyzed, or died. Such tragedies were not to be repeated. With the then-unknown threat of AIDS transmitted by infected blood, it became crucial to source safe, uninfected blood for the production of hepatitis B vaccines. Advancements in molecular science led to the discovery of the common “a” antigen present in all serotypes in both humans and animals. Consequently, a prototype yeast recombinant HB vaccine was formulated, safety-tested, and implemented in Singapore as a collaboration between the International Agency for Research in Cancer/WHO and the Singapore Government. I was then appointed by the Singapore government and IARC/WHO (International Agency for Research on Cancer) to oversee the safety in the manufacture and implementation of the vaccine. Then Prime Minister of Singapore, Mr. Lee Kuan Yew, who mandated the directive to me and my team, insisted on "300% safety, not just 100%." Together with my team and WHO oversight, we rejected several unsafe vaccines and identified vaccine-escape mutants in plasma vaccines that were over-treated with chemicals, which damaged the epitopes of the “a” antigen. This product was rejected. Similar Vaccine Escape Mutants (VEMs) arose with the Pfizer mRNA. Instead of inactivation, nine chemicals were used, including the deep-freezing agent phosphophenolglycol. I believe these VEMs on the Covid mRNA are the cause of the continuous eruption of spike mutants ranging from Delta to Omicron variants seen today, as humans have become reservoirs for these mutants. On my 80th birthday, July 4, 2019, 34 years since the WHO consultation, I announced the complete elimination of HBV and associated lethal liver failures and liver cancer at a Duke-NUS lecture (video below). SARS-2/COVID-19 In October 2018, my wife and I returned from a Yangtze River Cruise where we had admired the beautiful and ancient industrial city of Wuhan, home to 8 million people. START OF THE COVID PANDEMIC: January 2020 We woke to the news that Wuhan was besieged by a lethal coronavirus, resulting in thousands dead daily and several more thousands hospitalized until hospitals reached full capacity. Field hospitals were erected within days. Doctors and nurses arrived from all over China to provide aid; tragically, around a thousand of them died. Within a week, top Chinese scientists had determined the molecular structure of the coronavirus, which was dissimilar to any of the known viruses in their archives. The molecular structure seemed akin to the USCDC's patented invention (No. 7220852/B1 filed on May 22, 2004), with the addition of an HIV glycoprotein insert in the spike protein (later confirmed by Nobel Laureate Prof. Luc Montagnier). China disseminated information on the epidemic and the virus through premier journals and transmitted details to the International Genomic Bank. They invited the WHO in January 2020, who discovered many corona viruses but not this particular virus. Singapore We learned from the news that SG Prime Minister's wife, Ho Ching, chairman of Temasek Holdings, a Singapore investment company, had invested nearly S$3 billion in Pfizer/BioNTech and had initiated the procurement of Pfizer mRNA vaccines, Moderna, and plans for establishing vaccine manufacturing in Singapore. Pfizer and mRNA Vaccines Publications in JAMA 2021 showed that Pfizer was 98% effective. Six of my senior academic staff on the board of journals agreed with me that the end points for assessing efficacy were symptoms. (Later, a US Texas judge in 2022 ordered the FDA to release 55,000 pages showing thousands of deaths and serious adverse reactions. The US Supreme Court in 2022 also accepted Senator Robert Kennedy's charge that mRNA vaccines are not vaccines.) These were not the usual endpoints like antibody levels and virus absence in recipients. This was open to "ghost papers," which we had discovered at WHO. I alerted our three Ministers who know me and the 14 medical experts, "The Pfizer mRNA vaccines are not safe for mass immunization as the live lethal virus is still present in the mRNAs." Mandatory Vaccination Then, we received notice from our MOH (Ministry of Health) that all hospital and clinic staff, workplaces, and schools must be vaccinated or they cannot work. Retirement I was then 82 years old, and my mission after being recalled/returning from Cambridge with an MD in Cancer Immunology was completed. However, with my vast experience with vaccines, I continued to advise our MOH privately, as well as colleagues and friends in our country and worldwide. Request to MOH to Release Sinovac A full-length inactivated COVID virus vaccine, Singapore had 20,000 doses of Sinovac in stock. When the new Delta variant infected frontline workers in five public hospitals and Changi Airport in May 2021, I advised our Ministers that the mRNA vaccines were not preventative and to use Sinovac lest our hospitals be overwhelmed by infections. I also informed Ministers that many individuals with allergies cannot take mRNA vaccines and to release the Sinovac. This news was leaked, and I was chastised as peddling fake news by Prof. David Lye of the National Infectious Disease Center and senior Straits Times journalist Shamir Khalid. The Future COVID will remain for many years as the reservoirs of VEMs (Vaccine Escape Mutates) are evolving from failed protection in millions but causing deaths, delayed deaths, and illnesses. The 95% who received Pfizer and other mRNA vaccines, and not inactivated vaccines like Novavax, are developing new mutants. Losses Between 2021 and now, I have lost 34 senior medical colleagues. Most were working in institutions and had been vaccinated with Pfizer. I lost my eminent elder obstetrician aunt on March 31, 2022, who was infected by a Pfizer-vaccinated caregiver who had contracted the Delta spike mutant. She became too weak, stopped playing mahjong, stopped eating, and five days before she passed, she became blind. She died in my arms. I also lost my elder brother, a senior physician at 85, who received Moderna followed by two boosters of Pfizer. He contracted COVID and died two months later. How to Eliminate Wear masks to reduce aerosol transmission. Use antiviral drugs like Tamiflu, 75mg daily for 7 days. It is a potent neuraminidase inhibitor of COVID and the flu. As with most serious infections, take it early at the onset. Usually, ART is negative on day 2-3. Vaccine Research - With the many combinations of mutations, we need to find common antigens and make new inactivated vaccines. Sinovac and Sinopharm My wife and I have had three doses of Sinovac and two of Sinopharm. We have nucleocapsid spike antibodies and are well. 1.6 billion people, including children in 150 countries, have taken the Sinovac and Sinopharm vaccines. They are safe, protective, and have caused no fatalities. Countries can copy or learn from China. Save lives, not politics first. Retired, we stay at home and wear masks in crowded areas. Lessons It's essential to control and eliminate lethal airborne/aerosol infections. A healthy population is a robust workforce. A healthy youth is the future of our country. God bless all, Gabriel Oon Retired Professor of Medicine Former WHO Consultant for Biologicals for Human Use Some final comments by Aussie17: I am fully aware that there are people who are against any kind of vaccine, people who are against wearing masks, and people who believe there is no such thing as viruses. Whatever your opinion is on these matters, I’d just like to say that I know Professor Gabriel personally, and he does not have a single nefarious bone in his body. The world is such a divided place right now that even when you agree with someone 99%, people start calling names and scolding each other over the 1% disagreement, which only serves to deepen our divisions. I hope we can accept diverse views and come together. Signing off for now A17 Thank you for reading PharmaFiles by Aussie17. This post is public so feel free to share it. Share https://www.aussie17.com/p/my-story-by-professor-gabriel-oon
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    My Story - By Professor Gabriel Oon
    "Between 2021 and now, I have lost 34 senior medical colleagues. Most were working in institutions and had been vaccinated with Pfizer."
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