All Risk, Zero Benefit

 STOP THE MASS COVID-19 VACCINE ROLLOUT FOR CHILDREN AND YOUNG PEOPLE.

TEN REASONS WHY CHILDREN AND YOUNG PEOPLE SHOULD NOT GET THE COVID-19 VACCINES.

1. Children and young people have a mostly mild or asymptomatic presentation when infected with SARS-CoV-2. They are at near-zero risk of death from COVID-19.

2. There is an unusually high rate of reported adverse events and deaths following the COVID-19 vaccines compared to other vaccines. Some adverse events are more common in the young, especially myocarditis. Where potential harm exists from an innovation and little is known about it, the precautionary principle dictates to first do no harm. Better safe than sorry.

3. Medium and long-term safety data about the COVID-19 vaccines are still lacking. Children and young people have a remaining life expectancy of 55 to 80 years. Unknown harmful long-term effects are far more consequential for the young than for the elderly.

4. Vaccination policies rely on expected benefits clearly outweighing the risk of adverse events from the vaccination. The risk-benefit analysis for the COVID-19 vaccines points to a high potential risk versus no benefit for children and young people.

5. Transmission of SARS-CoV-2 from children to adults is minimal and adults in contact with children do not have higher COVID-19 mortality.

6. It is unethical to put children and young people at risk to protect adults. Altruistic behaviors such as organ and blood donation are all voluntary.

7. Several prophylactic treatments as well as the COVID-19 vaccines are available to high-risk individuals so they can protect themselves.

8. Natural immunity from infection with SARS-CoV-2 is broad and robust and more effective than vaccine immunity, especially in combating variants. Children and young people are safer with natural immunity.

9. There are several prophylactic (preventive) protocols and effective treatments available to children and young people with comorbidities.

10. Vaccinating children and young people is not necessary for herd immunity. After a year and a half of the pandemic, most people either have pre-existing immunity from other coronaviruses, have recovered from COVID-19 or have been vaccinated.

THERE IS THUS NO MEDICAL OR PUBLIC HEALTH CASE FOR THE MASS VACCINATION OF CHILDREN AND YOUNG PEOPLE, OR FOR COERCIVE OR RESTRICTIVE MEASURES AFFECTING THOSE WHO ARE UNVACCINATED. 

https://twitter.com/federicolois/status/1415347339171090433?s=20

Justin Myles Holmes,

14 July 2021: 

The presumption that preventing spread blindly, without regard to risk, was some kind of public health lightbulb is so frustrating.

All of these things also prevented spread through the low-risk tier, which delayed immunity and extended misery.  

Surely this is obvious by now.

Listen to some doctors here 

TAKE 

ACTION.

SAVE

LIVES. 

REPORT ADVERSE VACCINE EVENTS IN CHILDREN AND YOUNG PEOPLE.

Checklist

What will I need to fill out the report?

• Patient information (age, date of birth, sex)

• Vaccine information (brand name, dosage)

• Date, time, and location administered

• Date and time when adverse event(s) started

• Symptoms and outcome of the adverse event(s)

• Medical tests and laboratory results (if applicable)

• Physician’s contact information (if applicable)

In United States , click here . 

In United Kingdom, click here.

In Canada, click here. 

In Germany, click here. 

In Europe, click here. 

In South Africa,  click here. 

In Austria, click here. 

In Switzerland,  click here. 

In New Zealand, click here. 

In Australia, click here. 

In the Netherlands, click here. 

In Belgium, click here. 

In Ireland, click here. 

In Singapore, see here. 

In Malaysia, see here. 

Reporting systems for vaccine-associated adverse events are intended to raise red flags to guide definitive investigation. Examples include the VAERS system (USA), EudraVigilance (EU) and the Yellow Card system (UK). As with severe disease and mortality associated with a recent positive SARS-COV-2 test, vaccine-associated events may result directly from the vaccine (the vaccine is causal) or reflect unrelated background disease that is not related to the vaccine. The voluntary or non-enforced nature of reporting also means that actual rates of reported events may represent only about 10% of the true rate.

These databases serve a vital function in identifying the occurrence of unusual events or higher than expected rates, spurring urgent investigation to ascertain the cause and, in some circumstances, a halting of or withdrawal of the vaccine. This is critical as mass vaccination moves beyond controlled trials into populations who differ from the clinical trial population, or where rare but critical events are likely to have been missed in the smaller trial group. The rise in reports of adverse events in these three databases since the introduction of COVID-19 vaccines, which were introduced after relatively short trial periods, is an example of these systems working, and is intended to trigger urgent action to review safety and potential causality.

https://www.hpra.ie/homepage/about-us/report-an-issue/covid-19-vaccine-adverse-reaction