Discover more from Praying Mantis
If you missed Part 1, click here:
On a global scale, the FDA is considered the gold standard - partly because its rigorous approval process is onerous, costly, and lengthy. However, if there is no other treatment available, new therapies can be ushered to market under the umbrella of an “Experimental Use Authorization”. Basically, the notion is “We need a solution, this is better than nothing – it’s a risk we can assume.”
If a cost-effective alternative such as HCQ + Zinc exists, EUA’s are unavailable to Big Pharma. Clearly, there is more excitement to push say, Regeneron at $3200 a course, than therapies that are practically free. Our current healthcare system offers no incentive to fund clinical trials for patent expired therapies, even if they could save the world.
While we are on the money subject, an EUA also exempts the manufacturer from any product liability. When a person signs an informed consent, they assume the inherent risks and waive any future claims arising potential adverse effects. See how EUA’s benefit Big Pharma on the front and on the back end? Moreover, note how preventive measures such as Ivermectin, Zinc and Vitamin D (among others) have been notably downplayed by the media. One of the many questions we must ponder.
Under the guise of a pandemic, certain companies have benefitted enormously. Take a look at Moderna and Pfizer’s performance since February 2020. May I rest my case?
What I am redacting on these pages nothing new under the sun. The MD’s who bravely raised the alarm last year were silenced, de-platformed, threatened with loss of license or maligned. You will not read about this in corporate owned media. Strangely enough, this narrative has much in common with the allied air dropped pamphlets in WW2 because we are enmeshed in an information war.
Let’s further dissect this situation. Just because something is safe doesn’t mean it works. Or if it works it may not necessarily be safe. Does FDA approved oxycodone ring a bell? In the long run, that mistake contributed to the opioid crisis that continues to devastate entire communities and families.
There is a reason why clinical research is conducted by phases, notably excluding pregnant women or the possibility of conception from most trials (Google thalidomide babies). Why then is an experimental gene therapy been administered to expectant mothers and young children? This defies logic and is unprecedented in modern FDA history.
Per a study conducted in Japan, at 48 hours the bio-distribution of the lipid nano-particles containing the mRNA concentrates in the bone marrow, lymph nodes and female reproductive organs. The reports of absent periods, heavy periods or irregular menstruation cycles in young girls after inoculation correlates to the red flags notable scientists were calling out as the vaccine rolled out in 2019. What if this affects the fertility of our daughters and grandaughters?
Understandably, there is a cohort of the population that bears a higher risk when contracting the China virus (and influenza to be precise). However, this does not include healthy adolescents, college students, millennials or GenX’s and arguably, even some Boomers. Why has the youth been pressured, coerced, incentivized, fearmongered or mandated to inoculate an experiment with unknown long-term risks? Does this not puzzle you? It confounds me.
This we do know. The lockdowns offered the perfect excuse to change the rules of the game: Mail-in ballots. For more insight you may want to start from the beginning:
In this following installment I explore the controversial FDA approval which at best is confusing and at worst, misleading. Here you go:
I write in chapters. To get the big picture, click here:
If this is helpful to you, someone else might appreciate the information:
Hungry for more information? Listen to Dr. Robert Malone (inventor of the mRNA vaccines technology), Steve Kirsch (savvy entrepreneur in healthcare tecnology) and Bret Weinstein. This is a long discussion that covers many topics but it is a 5 course meal of knowledge. It is time stamped so you can fast forward to a particular topic:
How to save the world, in three easy steps - Bret Weinstein, Robert Malone, Steve Kirsch