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OXFORD, England, February 22, 2021 (LifeSiteNews) — Oxford University’s Vaccine Group is recruiting children from the age of 6 to participate in an experimental COVID-19 vaccine trial, despite young children facing almost no danger from the virus.
“We have a new COVID-19 study open for recruitment. If your child is aged 6-17 years and in good health they may be eligible to participate,” the group tweeted earlier this month.
We have a new COVID-19 study open for recruitment. If your child is aged 6-17 years and in good health they may be eligible to participate. Click on the link to find out more. https://t.co/4zbqIEI9LT #OxfordVaccineGroup #OxfordVaccine #Covid19 pic.twitter.com/4IFvVWWbj7
— Oxford Vaccine Group (@OxfordVacGroup) February 13, 2021
The study seeks to assess the safety and effectiveness of the Oxford/AstraZeneca COVID-19 vaccine (also known as ChAdOx1 nCoV-19 ), and enroll 300 children to participate. Up to 240 kids will be injected with the experimental COVID-19 vaccination while the rest will receive as a control group, a licensed vaccine for Meningitis B (MenB, Bexsero).
British mental health ethicist and academic, Niall McCrae condemned the encouragement of parents to enter their children in a COVID-19 vaccine trial as “very wrong,” Church Militant reports.
“Children should not be lab rats for the benefit of Big Pharma and the Great Reset. I would go as far as saying this is tantamount to child abuse,” Dr. McCrae warned.
“Vaccinating children against coronaviruses is unjustifiable, given the minimal risk of infection and transmission,” The King’s College lecturer continued. “I sat on a National Health Service (NHS) ethics committee for 11 years, and I'm very worried about the apparent disregard for established scientific and ethical standards to serve the COVID regime.”
Concerns over the health and safety of the human test subjects in Pfizer's European COVID vaccine study have caused two eminent doctors to launch a petition calling for an immediate halt to those studies.
On December 1, 2020, Dr. Michael Yeadon, an ex chief of research at Pfizer and Dr. Wolfgang Wodarg, a lung specialist and former department head of public health lodged an appeal to the EMA, the European Medicine Agency responsible for approving drugs across the EU, asking them to suspend the ongoing Pfizer/BioNtech COVID vaccine study on BNT162b (EudraCT number 2020-002641-42).
LifeSite is joining Drs. Yeadon and Wodarg in their call for an immediate suspension of this study and we are encouraging people to co-sign their petition to the EMA which is to be found in the petition section on this page.
Please SIGN and SHARE this important petition, and then please contact the EMA at the address listed below, in the 'For More Information' section.
In their application to the EMA, Drs. Yeadon and Wodarg give the following reasons why the Pfizer study could pose dangers to the health and safety of the study participants:
- First, the doctors say that the study design must be improved as the highly inaccurate PCR test is currently being used to detect the presence of COVID in the study participants. This means that the efficacy of the vaccine is in doubt. The doctors recommend changing from the PCR test to Sanger sequencing.
- Second, and more important, the doctors advocate animal testing of the vaccine to exclude the possibility of the risks to the life and health of human participants from known side-effects of other similar studies on corona viruses.
These side-effects can include: an exaggerated immune response when the subject comes into contact with the "real world" virus; possible infertility of an "indefinite duration" for women; severe allergic responses to polyethylene glycol which is contained in the mRNA vaccine being tested by Pfizer; and, other latent, serious side effects which, because of the short duration of the study, may only become known well after the conclusion of the study.
Because of these unacceptable risks to the life and health of the Pfizer/BioNtech COVID vaccine study participants, we are joining with Drs. Yeadon and Wodarg as co-signers of their petition to the European Medicine Agency, asking for an immediate halt to these studies.
Thank you for SIGNING and SHARING, today!
And, after you have signed this petition, please send the sample email in the section below to the official European Medicine Agency email: [email protected]
FOR MORE INFORMATION:
Subject: Please act on the petition of Dr. Wodarg and Dr. Yeadon and stay the Phase III clinical trial(s) of BNT162b
Dear Sir or Madam,
I am hereby co-signing the petition of Dr. Wodarg and Dr. Yeadon to support their urgent request to stay the Phase III clinical trial(s) of BNT162b (EudraCT Number 2020-002641-42) and other clinical trials. The full text of the petition of Dr. Wodarg and Dr. Yeadon can be found here: https://2020news.de/wp-content/uploads/2020/12/Wodarg_Yeadon_EMA_Petition_Pfizer_Trial_FINAL_01DEC2020_EN_unsigned_with_Exhibits.pdf
I hereby respectfully request that EMA act on the petition of Dr. Wodarg and Dr. Yeadon immediately.
Regards, [Your name]
**Photo Credit: Shutterstock.com
Established scientific and ethical standards with regards to experimentation on humans, can be found in the Nuremburg Code of 1947, which came about as a result of the post-World War II trials and convictions of Nazi doctors who had conducted deadly experiments, without the subjects’ consent, on prisoners of war.
The Nuremberg Code’s first principle provides the strict conditions for establishing voluntary consent, including that the subject “should have legal capacity to give consent,” along with “sufficient knowledge and comprehension of the elements of the subject matter involved.” In addition, such consent “may not be delegated to another with impunity.”
Thus, McCrae urged parents to understand “that they will be held responsible, not only the pharma company, for any serious harm caused by this experiment” on their child.
The sixth principle of the Code affirms that the “The degree of risk to be taken should never exceed that determined by the humanitarian importance of the problem to be solved by the experiment.”
Given that the threat of a COVID-19 infection remains essentially “irrelevant” to school-aged children due to their 99.997% survival rate, McCrae notes that subjecting them to any dangers from an experimental vaccine remains “unjustifiable.”
Other moral concerns derive from the fact that the development of the AstraZeneca experimental vaccine used the HEK-293 cell line made from fetal cells harvested from the kidney tissue of a baby girl who was aborted in the Netherlands in 1972.
As confirmed by the Vatican’s recent “Note on the morality of using some anti-Covid-19 vaccines,” at the very least, to consider the use of such a morally tainted vaccine, there must first be a “grave danger” which no one has alleged is the case for children.