What is an Emergency Use Authorization
by Joan River l September 2, 2021
Dear Brian,
I have been asking myself WHY the FDA ever authorized the development of and distribution of Covid-19 vaccines in the first place.
What is an Emergency Use Authorization (EUA)?
An Emergency Use Authorization (EUA) is a mechanism to facilitate the availability and use of medical countermeasures, including vaccines, during public health emergencies, such as the current COVID-19 pandemic.
Under an EUA, FDA may allow the use of:
– unapproved medical products,
– unapproved uses of approved medical products in an emergency to diagnose, treat, or prevent serious or life-threatening diseases or conditions when certain statutory criteria have been met, including that there are no adequate, approved, and available alternatives.
When the SARS-COV-2 (old name 2019-nCoV) was introduced to the world in December of 2019, I really wasn’t too concerned. After all, viruses are a part of life here on planet earth. Every day we are exposed to viruses, bacteria, fungi and parasites. In fact, we have billions and trillions of resident microbes of all varieties living in our bodies and on our skin.
Most people by now are aware of the Microbiome and some people are aware of the Virome. These are the resident populations of bacteria and viruses living in and on our bodies.
We live in harmony with microbes in an ecological balance. As viruses circulate through the environment, some people will develop symptoms known as a viral illness, while most people do not develop illness.
Generally speaking, a viral illness represents a Detoxification Event of the body.
That is why you feel horrible during the illness and for the most part feel wonderful afterwards. The body goes through these detoxification events periodically throughout the lifespan of the body as part of the body’s routine maintenance program.
There are some scientists who posit, with good evidence, that viruses and bacteria are not actually substances that come into the body from the outside environment, but rather are formed within the body to deal with the dead cells that naturally accumulate within the body, and that it is the toxins produced as a result of this clean-up work being done by intrinsically created viruses and bacteria that are the true cause of the symptoms.
People who go through a ‘Detox” program sometimes experience a phenomenon known as “Herxheimer Reaction” when the toxins are liberated faster than the body can eliminate them, and the symptoms are described to be ‘flu-like’ symptoms. Brian, I’m no expert on this theory of viral illness but it’s intriguing and I’m looking into it.
So, like I said, I wasn’t too concerned about a viral illness being discussed.
But after several weeks, it was evident that this ‘new’ virus was becoming the topic of every conversation and was not ‘going away.’ Some people in China and Europe were developing significant illness attributed to this declared ‘novel’ virus and cell phone videos from China were showing people dropping dead in the streets, apparently without warning.
So, I did what I always do and I began paying attention to what the scientists and doctors whom I had come to trust as being persons with integrity were saying about this new virus, or ‘novel’ virus as it was being called.
Within a short period of time, I became aware of various therapeutic regimes being used here in the United States and around the world that were having efficacy in treating the viral illness.
There were Homeopathy protocols, protocols using only nutritional supplements in therapeutic dosages, protocols using a combination of therapeutic dosages of nutritional supplements and standard over the counter drugs and prescription drugs. Even early on into the pandemic, doctors were having great success in treating patients and saving lives with these readily-available and inexpensive protocols.
There was a large worldwide initiative to re-purpose old drugs to use in treating the viral illness. Hydroxychloroquine, an anti-parasitic drug, was one of the first drug to be identified as being beneficial, and soon Pulmicort (Budesonide), an Asthma drug, and Ivermectin, another anti- parasitic drug, were being utilized by doctors to treat the viral illness.
Many people are suffering needlessly because they are not aware that effective prevention and treatments exist for the illness known as COVID-19, and others because their doctors refuse to utilize the protocols.
People need to realize that these protocols are accessible to them because even if their doctor won’t acknowledge them, there are many doctors in the U.S. that do, and through telemedicine consults these protocols can be prescribed.
And for those people who don’t want to use prescription drugs, the protocols using only therapeutic dosages of nutritional supplements are also very beneficial.
It’s important for people to realize that they can be empowered to learn how to care for their body and avoid living in fear of a dreaded illness for which there is no hope of avoiding.
This article links to many of the therapeutic regimes being used to treat Covid-19 illness and includes resources on how to obtain these treatments:
https://www.onedaymd.com/2021/04/dr-richard-bartlett-inhaled-budesonide.html
So, I really want to know WHY an EUA was given for the development of a ‘vaccine’ for Covid-19 illness, when there were several effective treatment protocols for the treatment of the illness.
If treatments exist, WHY create a ‘vaccine’?
But at great expense, these ‘vaccines’ WERE created and have now become the ONLY recognized solution for controlling Covid-19 illness.
Was the Emergency Use Authorization for the ‘vaccines’ obtained fraudulently?
It certainly seems so to me.
And if so, WHY the push for the entire population to receive these injections?
– Joan
*****
Joan sent us the following link:
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