[Note: This thread is based on my personal research, not copied from someone else. Quotations are provided as needed]
PART I
AstraZeneca's vaccine was approved by the World Health Organization in February, 2021 and is being currently distributed worldwide. But two long term care patients died in South Korea within days of being vaccinated. As usual, the public health officials tried to suggest that there was no "direct link". And that is the real issue. The truth is never presented honestly. Over and over again, there is a denial of a direct link (unless it suits the public health officials). "Several French hospitals are pausing or slowing down AstraZeneca vaccination programmes for their staff because severe - albeit temporary - side effects have caused many employees to need sick leave, causing severe logistical problems in already over-stretched services." So it could mean that the cure is worse than the disease.
While the mRNA vaccines are troubling, AstraZeneca's COVID-19 vaccine should be very troubling, particularly to third world countries. There are several reasons for this: (1) it is not a genuine vaccine in the traditional and accepted sense; (2) it was improperly tested; (3) it was rushed to market without proper evaluation of all the actual and potential issues; (4) those who have funded it have a conflict of interest in the profits they will reap from it; and (5) the people behind this vaccine are also the people seriously behind Eugenics.
1. AstraZeneca's vaccine is not a genuine traditional vaccine
According to the World Health Organization "The ChAdOx1-S/nCoV-19 [recombinant] vaccine is a replication-deficient adenoviral vector vaccine against coronavirus disease 2019 (COVID-19). The vaccine expresses the SARS-CoV-2 spike protein gene, which instructs the host cells to produce the protein of the S-antigen unique to SARS-CoV-2, allowing the body to generate an immune response and to retain that information in memory immune cells." In other words it uses another mammalian virus to trick the body into thinking that coronavirus has entered in.
This is further explained here:"A coronavirus vaccine known as ChAdOx1 nCoV-19 or AZD1222 was developed by the University of Oxford and AstraZeneca to treat severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection (the cause of COVID-19). In this vaccine, a modified version of a chimpanzee adenovirus (ChAdOx1) is used which can enter human cells but not replicate inside. A gene for the coronavirus vaccine was added into the adenovirus DNA, allowing the vaccine to target the spike proteins that SARS-CoV-2 uses to enter human cells." https://www.news-medical.net/health/What-are-Adenovirus-Based-Vaccines.aspx
2. AstraZeneca's vaccine was improperly tested
a) It was tested in only the UK, Brazil, and South Africa, but the results for S. Africa were obfuscated.
b) There was only one medical doctor on the research team. The rest were all PhD's. For a medical study, this appears to be rather irresponsible.
c) It was only an "interim" analysis of results. Yet the vaccine is being distributed.
d) It was limited to ages 18-55 in the primary trials. Those who need it most are in the 65 to 85+ age group, but they were excluded, probably because that would have been the death of the vaccine!
e) While South Africa is mentioned, the total number of participants (11,636 out of a total of 23,848) only included those from the UK and Brazil.
f) While the control (or placebo) is always supposed to be a saline solution, "meningococcal group A, C, W, and Y conjugate vaccine" -- another vaccine -- was used unfairly to skew the results: As a result "From 21 days after the first dose, there were ten cases hospitalised for COVID-19, all in the control arm; two were classified as severe COVID-19, including one death." Using the term "control arm" is rather unusual (if not silly), but the researchers had no business complicating things by administering a vaccine for meningitis as a control.
g) A standard dosage was not used consistently, and for all participants. That in itself should have nullified the trials.
h) Efficacy was tested against symptoms, but also using the discredited PCR test (assuming that the same faulty procedure was used which has skewed results everywhere).
i) None of the participants was actually exposed to real existing cases of coronavirus patients under treatment, which means that no one knows how good the immunization really is (or is not).
j) The manufacturers of the vaccine were actually separate entities from AstraZeneca, so technically it was not even an AstraZeneca vaccine."The recombinant adenovirus for ChAdOx1 nCoV-19 was manufactured and vialed by Advent (Pomezia, Italy), and additional batches produced by COBRA Biologics (Keele, UK) and vialed by Symbiosis (Sterling, UK)."
PART I
AstraZeneca's vaccine was approved by the World Health Organization in February, 2021 and is being currently distributed worldwide. But two long term care patients died in South Korea within days of being vaccinated. As usual, the public health officials tried to suggest that there was no "direct link". And that is the real issue. The truth is never presented honestly. Over and over again, there is a denial of a direct link (unless it suits the public health officials). "Several French hospitals are pausing or slowing down AstraZeneca vaccination programmes for their staff because severe - albeit temporary - side effects have caused many employees to need sick leave, causing severe logistical problems in already over-stretched services." So it could mean that the cure is worse than the disease.
While the mRNA vaccines are troubling, AstraZeneca's COVID-19 vaccine should be very troubling, particularly to third world countries. There are several reasons for this: (1) it is not a genuine vaccine in the traditional and accepted sense; (2) it was improperly tested; (3) it was rushed to market without proper evaluation of all the actual and potential issues; (4) those who have funded it have a conflict of interest in the profits they will reap from it; and (5) the people behind this vaccine are also the people seriously behind Eugenics.
1. AstraZeneca's vaccine is not a genuine traditional vaccine
According to the World Health Organization "The ChAdOx1-S/nCoV-19 [recombinant] vaccine is a replication-deficient adenoviral vector vaccine against coronavirus disease 2019 (COVID-19). The vaccine expresses the SARS-CoV-2 spike protein gene, which instructs the host cells to produce the protein of the S-antigen unique to SARS-CoV-2, allowing the body to generate an immune response and to retain that information in memory immune cells." In other words it uses another mammalian virus to trick the body into thinking that coronavirus has entered in.
This is further explained here:"A coronavirus vaccine known as ChAdOx1 nCoV-19 or AZD1222 was developed by the University of Oxford and AstraZeneca to treat severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection (the cause of COVID-19). In this vaccine, a modified version of a chimpanzee adenovirus (ChAdOx1) is used which can enter human cells but not replicate inside. A gene for the coronavirus vaccine was added into the adenovirus DNA, allowing the vaccine to target the spike proteins that SARS-CoV-2 uses to enter human cells." https://www.news-medical.net/health/What-are-Adenovirus-Based-Vaccines.aspx
2. AstraZeneca's vaccine was improperly tested
a) It was tested in only the UK, Brazil, and South Africa, but the results for S. Africa were obfuscated.
b) There was only one medical doctor on the research team. The rest were all PhD's. For a medical study, this appears to be rather irresponsible.
c) It was only an "interim" analysis of results. Yet the vaccine is being distributed.
d) It was limited to ages 18-55 in the primary trials. Those who need it most are in the 65 to 85+ age group, but they were excluded, probably because that would have been the death of the vaccine!
e) While South Africa is mentioned, the total number of participants (11,636 out of a total of 23,848) only included those from the UK and Brazil.
f) While the control (or placebo) is always supposed to be a saline solution, "meningococcal group A, C, W, and Y conjugate vaccine" -- another vaccine -- was used unfairly to skew the results: As a result "From 21 days after the first dose, there were ten cases hospitalised for COVID-19, all in the control arm; two were classified as severe COVID-19, including one death." Using the term "control arm" is rather unusual (if not silly), but the researchers had no business complicating things by administering a vaccine for meningitis as a control.
g) A standard dosage was not used consistently, and for all participants. That in itself should have nullified the trials.
h) Efficacy was tested against symptoms, but also using the discredited PCR test (assuming that the same faulty procedure was used which has skewed results everywhere).
i) None of the participants was actually exposed to real existing cases of coronavirus patients under treatment, which means that no one knows how good the immunization really is (or is not).
j) The manufacturers of the vaccine were actually separate entities from AstraZeneca, so technically it was not even an AstraZeneca vaccine."The recombinant adenovirus for ChAdOx1 nCoV-19 was manufactured and vialed by Advent (Pomezia, Italy), and additional batches produced by COBRA Biologics (Keele, UK) and vialed by Symbiosis (Sterling, UK)."
- 2
- Show all