Hercule Poirot uses his little grey cells to solve mysteries. We have many mysteries that have arisen from the start of the COVID-19 pandemic.
We have learned a lot and continue to learn. However, the vaccines are being expedited at a rate never seen before. Vaccines that typically take five years will be released to the public in less than a year.
My little grey cells are telling me that there are mysteries associated with all new vaccines that need full disclosure. Here are my questions that I would like to have answered so that the public can make wise decisions on each of the vaccines.
Should a company that has never made a vaccine for humans be allowed to short-circuit the FDA guidelines for new vaccine release? If so, what are the risks?
What are the short-term and long-term risks/side effects of vaccines made outside the normal vaccine process, such as using modified RNA or modified DNA?
Are all common side effects, systemic side effects, and adverse events fully understood and available to the public?
Who or what group of people should fully evaluate the results of clinical trials?
Should home-administered vaccines be available to the public? How are records kept?
What is the process for tracking those taking vaccinations? How is verification to be done?
What are the conditions that a person can legally/morally refuse a vaccine?
If transfection is used to induce a vaccine into the body, what long-term guarantee is given that the human genome is not permanently affected? What is the recourse if it is? What potential future health risks are associated with an altered human genome?
If the transfection process used, what guarantees that the human genome is not permanently affected?
Is there a risk of a new vaccine genetically modifying the human genome?
What are the short-term and long-term effects of synthetic RNA and DNA?
Should nanotechnology be incorporated into vaccines?
What controls are there for any nanotechnology introduced into the human body?
What are the contraindications for the new vaccine?
What trials have been done to identify the new vaccine interfering with existing medications (over the counter and prescription)?
What is full disclosure required for any public official providing public health policy guidance/information available to the public each time that he or she gives such guidance/information?
There are probably another dozen questions that my little grey cells could conceive, but these are the ones that have come to me spending a little bit of time today.
There are many risks associated with any new medicine. We are getting ready to vaccinate millions of citizens and the expedited process will have risks. We need to know and fully understand those risks. And what happens when those risks are underestimated?
Live Long & Enjoy Life! – Red O’Laughlin – RedOLaughlin.com