By Dr. John Reizer
Where there is a potential risk associated with medical products or procedures, human beings must be afforded the freedom to choose whether or not they want to receive the services. This is known as informed consent.
Any healthcare provider or government entity that forces a person or the general population to take or receive a therapeutic drug/procedure that carries a potential risk to said individuals’ health or wellbeing, without affording them the choice to opt-out would be guilty of medical rape. I believe that informed consent is enforceable at all times and without limitations or exceptions, such as when an epidemic or pandemic has been declared by health officials.
There is not one vaccine product in existence that does not present potential risks to human beings. One of the disclaimers always written in all drug inserts that have been used to legally protect the pharmaceutical industry is a statement that warns the consumer not to take the product if they are allergic to any of the ingredients. How would a person know if they are allergic to the ingredients if they have never taken the concoction?
The link below will take you to a website where you can read the product inserts for every vaccine on the market. Read the information (the fine print) that clearly explains the risks associated with taking these hazardous products. There are inherent risks associated with all the products or the risks are unknown according to the vaccine makers.
Many of the problems associated with vaccine injuries occur months and years after the poisons are administered to unknowing victims.
Keep in mind, the COVID-19 vaccines soon to be released have been granted full liability immunity by the federal government. Why do you think that might be? The answer: they’re anticipating massive problems.
Granting vaccine makers full immunity against health consumers’ injuries is not exactly a vote of confidence by the federal government concerning the vaccine product.
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