Comments by "Orionishi" (@orionishi6737) on "Dr. John Campbell" channel.

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  288.  @o4pureh2o  And I have found the kicker. That isn't the full amount of information...once again, y'alls motto, out of context. The unvaccinated, as it's labeled in that particular data, are only the people that are completely unknown...the vaccinated and unvaccinated that are accounted for in the Australian pop. are grouped together. There is apparently another report that breaks that group of the pop. down further into vaccinated and unvaccinated, the different vaccines they got, the amount of boosters and so on. Also, it is not accounting for the data on age of deaths, other underlying factors and the amount of people that are vaccinated. The higher amount of deaths is happening at majority in older at risk groups who were vaccinated. Not every day people living their lives. Basically, because everybody there is vaccinated, the people who are frail and old or already sick who then catch it still, are counted as vaccinated. It's a statistic that was expected to go up once everybody was vaccinated...because you know people are still going to die from things. I know y'all think when they claim that vaccines help stop infection they mean individually... that's not what they mean. Vaccines don't stop infection like that. They slow the spread of it by giving people immunity so that they aren't sick and contagious for as long a period of time. Which stops as many people from being infected... especially since y'all can't just stay home when you are sick or at least wear a mask when you go in public and might have something....cause we both know you kept going out and about, even before Covid when it was just the flu...you are definitely the type. You don't have to fear monger....the actual truth is out there...this is why large sets of data being cherry picked out of context is misleading and dangerous.
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  306.  @foxwylde2510  sigh...not exactly....you are almost there. Regardless, this history humbles vaccine scientists. They know that they hold people’s lives in their hands. As stated by Dr. Maurice Hilleman, perhaps the most prolific vaccine scientist in history, “I never breathe a sigh of relief until the first few million doses are out there,” (Personal communication, Paul Offit, 2004). For this reason, scientists and public health officials carefully analyze and continually monitor the data related to every vaccine before, during and after it becomes available. Even with this history in mind, some reasonably wonder about the COVID-19 vaccines because they have not previously been approved for use in people. But here, too, we can be confident in what we know: mRNA vaccine Although COVID-19 mRNA vaccines are new, this type of vaccine has been studied in people before. mRNA vaccines against HIV, rabies, Zika and flu have been tested in phase 1 and phase 2 trials in people. The technology has also been used in clinical trials as a way to treat some cancers. Even though these products have not been licensed for use in people, these efforts provided important information about mRNA technology and its safety. mRNA is made and used in protein production in all cells of our bodies. As such, cells have mechanisms in place to ensure that no protein is made in quantities greater than needed. One way this happens is that mRNA has a “poly(A) tail.” In the cytoplasm, this tail ensures mRNA decay. As the mRNA is used to make proteins in the cell, the length of the poly(A) tail decreases, until it is too short for the mRNA to continue being used as a protein blueprint. Once this happens, the mRNA breaks down and is removed as cellular debris. This process limits how long mRNA remains in the cytoplasm — and, therefore, how much protein is produced. As such, poly(A) tails ensure that the cell breaks down the vaccine mRNA in a timely manner. Likewise, this understanding allows scientists to design vaccine-delivered mRNA in a way that ensures it does not stay in the cell longer than needed to generate immunity.
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  408.  @BS-ge4ne  Regardless, this history humbles vaccine scientists. They know that they hold people’s lives in their hands. As stated by Dr. Maurice Hilleman, perhaps the most prolific vaccine scientist in history, “I never breathe a sigh of relief until the first few million doses are out there,” (Personal communication, Paul Offit, 2004). For this reason, scientists and public health officials carefully analyze and continually monitor the data related to every vaccine before, during and after it becomes available. Even with this history in mind, some reasonably wonder about the COVID-19 vaccines because they have not previously been approved for use in people. But here, too, we can be confident in what we know: mRNA vaccine Although COVID-19 mRNA vaccines are new, this type of vaccine has been studied in people before. mRNA vaccines against HIV, rabies, Zika and flu have been tested in phase 1 and phase 2 trials in people. The technology has also been used in clinical trials as a way to treat some cancers. Even though these products have not been licensed for use in people, these efforts provided important information about mRNA technology and its safety. mRNA is made and used in protein production in all cells of our bodies. As such, cells have mechanisms in place to ensure that no protein is made in quantities greater than needed. One way this happens is that mRNA has a “poly(A) tail.” In the cytoplasm, this tail ensures mRNA decay. As the mRNA is used to make proteins in the cell, the length of the poly(A) tail decreases, until it is too short for the mRNA to continue being used as a protein blueprint. Once this happens, the mRNA breaks down and is removed as cellular debris. This process limits how long mRNA remains in the cytoplasm — and, therefore, how much protein is produced. As such, poly(A) tails ensure that the cell breaks down the vaccine mRNA in a timely manner. Likewise, this understanding allows scientists to design vaccine-delivered mRNA in a way that ensures it does not stay in the cell longer than needed to generate immunity. The chances of adverse effects happening to anybody are slimmer than dieing from COVID-19...and y'all say that is like impossible, right?
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  594. This is just an ignorant lie. Not even close to true. The vaccines were almost done with phase 3 trials when we started to get them. Regardless, this history humbles vaccine scientists. They know that they hold people’s lives in their hands. As stated by Dr. Maurice Hilleman, perhaps the most prolific vaccine scientist in history, “I never breathe a sigh of relief until the first few million doses are out there,” (Personal communication, Paul Offit, 2004). For this reason, scientists and public health officials carefully analyze and continually monitor the data related to every vaccine before, during and after it becomes available. Even with this history in mind, some reasonably wonder about the COVID-19 vaccines because they have not previously been approved for use in people. But here, too, we can be confident in what we know: mRNA vaccine Although COVID-19 mRNA vaccines are new, this type of vaccine has been studied in people before. mRNA vaccines against HIV, rabies, Zika and flu have been tested in phase 1 and phase 2 trials in people. The technology has also been used in clinical trials as a way to treat some cancers. Even though these products have not been licensed for use in people, these efforts provided important information about mRNA technology and its safety. mRNA is made and used in protein production in all cells of our bodies. As such, cells have mechanisms in place to ensure that no protein is made in quantities greater than needed. One way this happens is that mRNA has a “poly(A) tail.” In the cytoplasm, this tail ensures mRNA decay. As the mRNA is used to make proteins in the cell, the length of the poly(A) tail decreases, until it is too short for the mRNA to continue being used as a protein blueprint. Once this happens, the mRNA breaks down and is removed as cellular debris. This process limits how long mRNA remains in the cytoplasm — and, therefore, how much protein is produced. As such, poly(A) tails ensure that the cell breaks down the vaccine mRNA in a timely manner. Likewise, this understanding allows scientists to design vaccine-delivered mRNA in a way that ensures it does not stay in the cell longer than needed to generate immunity.
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  600.  @bluecoffee8414  we used all the other vaccines before longterm trial phases were done too. They only have to make it through phase 3 trials to be deemed safe enough for the general use in the public. The COVID-19 vaccines hadn't finished phase 3 trials when we began to distribute them but they had made it through phase 1 and 2 trials. Shortly after that release they completed phase 3 trials. On top of that there had been a decade of use and testing on humans before 2020. Regardless, this history humbles vaccine scientists. They know that they hold people’s lives in their hands. As stated by Dr. Maurice Hilleman, perhaps the most prolific vaccine scientist in history, “I never breathe a sigh of relief until the first few million doses are out there,” (Personal communication, Paul Offit, 2004). For this reason, scientists and public health officials carefully analyze and continually monitor the data related to every vaccine before, during and after it becomes available. Even with this history in mind, some reasonably wonder about the COVID-19 vaccines because they have not previously been approved for use in people. But here, too, we can be confident in what we know: mRNA vaccine Although COVID-19 mRNA vaccines are new, this type of vaccine has been studied in people before. mRNA vaccines against HIV, rabies, Zika and flu have been tested in phase 1 and phase 2 trials in people. The technology has also been used in clinical trials as a way to treat some cancers. Even though these products have not been licensed for use in people, these efforts provided important information about mRNA technology and its safety. mRNA is made and used in protein production in all cells of our bodies. As such, cells have mechanisms in place to ensure that no protein is made in quantities greater than needed. One way this happens is that mRNA has a “poly(A) tail.” In the cytoplasm, this tail ensures mRNA decay. As the mRNA is used to make proteins in the cell, the length of the poly(A) tail decreases, until it is too short for the mRNA to continue being used as a protein blueprint. Once this happens, the mRNA breaks down and is removed as cellular debris. This process limits how long mRNA remains in the cytoplasm — and, therefore, how much protein is produced. As such, poly(A) tails ensure that the cell breaks down the vaccine mRNA in a timely manner. Likewise, this understanding allows scientists to design vaccine-delivered mRNA in a way that ensures it does not stay in the cell longer than needed to generate immunity.
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