Go and check at the website Revolution Radio, the chatroom and the archives for all past shows. You can listen to me live every Wednesday from 1pm - 3pm EST.

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Today we I am going to be reading an article I wrote called "Ineffectual Behavior, Medical Abuse and the FDA".

Let’s get started with todays topic!

What happens when people, who are conditioned to be passive and unable to deal with confrontation, eventually break because of oppression from an external source?

I would conclude that the reaction from the oppressed population suffering from this condition amounts to habitual ineffectual behavior that leads in circles, inevitably going nowhere. Outrage ensues but no actions to change this occurs. This is something I would like to explore.

Through our history we can see a pattern that emerges. One that is always a two-sided battle. The oppressors (the minority) and everyone else (the majority). The funny thing is that the minority always seems to come out on top even when the majority often "wins" the battles. Somehow the minority always seems to weasel it's way back into the equation. I think there are two major issues here.

First, people forget their history. It is true what George Santayana (1863 – 1952), who was a philosopher, essayist, poet and novelist, said, "Those who cannot remember the past are condemned to repeat it". This is a phrase that has been repeated since that time in one form or another but the the sentiment is, regardless, true. People do not pay enough attention to history and so they forget the consequences of doing so. Which leads to the second major issue.

Second, they forget the most important key to maintaining the condition of "freedom" for their fellow man. That the Law must be reiterated with every new generation. Always and forever. Without fail. There is no end to having to enforce our inherent rights against an enemy. There is no one and done scenario.

This is where I think people are missing the mark. At the very least it is naive to think it may be so easy and at the very worst is it laziness to think "we did it and the fight has been won, now I can forget about it and move on". There is a layer of selfish, unaccountability here. People are looking at it like this is a task to be checked off rather than a condition that must be eternally maintained.

Because of these two major issues currently in play today this will be the reason why we will never have any freedom for anyone or for that matter, freedom that will be long lasting. As long as these things are ignored on a large scale and people continue to slack-off in there obligations to this then the condition on this planet will remain the same. I would like to say that just standing up for our inherent human rights and saying "No!" to all false authority would do the trick, and to an extent that is true, but really this falls short if people do not address these underlying problems. Without people addressing these things in full, there is no amount of protest that will ever matter. The parasitic class will always try to climb to the top of every authoritarian ladder in order to wield control over others so to forget this is folly. There will always be a parasitic class. At least 1% of the worlds population will be born with genetic traits that cause the underlying condition of psychopathic behavior. This does not include the larger percentage of people who develop these traits by other external means after they are born due to sever traumatic experiences. And people forget this. It all amounts to operating ineffectually.

Let's explore some examples. There is more than one distraction taking place to set people down the wrong "rabbit-hole" that gets them to ignore these underlying issues. People are always asking, "Why?" but they should be asking, "How?"

One of these is the psy-op of "flat-earth" which targets mainly the truth-seeker communities and the modern Christian communities. This particular distraction causes those looking for any truth to focus on things that are ultimately irrelevant to the root cause that creates mass slavery on this planet. The root cause being the parasite class and their activities. Though I will be the first to say ... the Earth is NOT flat ... the shape of the planet makes no never-mind to a parasite class who is oppressing a population and enslaving them. Unfortunately, a lot of the truthseeker community and the modern Christian community are primed to buy, in wholesale, the fantasy that the parasite class constantly churns out for them. So it gets summed up all neat and pretty under the tag line, "NASA lies about everything so EVERYTHING is a lie!" It's a cowardly, naive, lazy and selfish stance to take because this allows the difficulty we face on this planet to at least remained contained and there seems to be some sort of limit. I have heard it more than once where a person (typically someone who is just a useful dupe) campaigning flatearth propaganda saying that exposing flat-earth is the MOST important issue on this planet and nothing is more of a problem than exposing this "lie" we have been told. Apparently, the lie about the shape of the planet trumps all other issues, including the rampant issue of child trafficking and child abuse taking place for the last several centuries. It makes me place all flatearth supporters at the metaphorical "child's table" because all it tells me is that they have not broken out of their child's view about reality, both the physical and the non-physical aspects of it. It tells me that they are not ready to take responsibility for themselves or for the state of the world. It's like watching a child have a temper tantrum because they have to clean their room or do some other inconvenient chore.

Another one of these distractions is the subject of veganism. Now, before people clutch at their pearly whites allow me to be clear. There is nothing wrong with being a vegan. If one can maintain a vegan diet in a healthy way that does not hurt themselves then I am in full support of this. I am also in the frame of mind that we must be healthy; mind, body and soul in order to be able to function at our most optimal level. When we, as an individual, are not healthy than we are ... again ... acting in ineffectual behavior. The issue is, unfortunately, most people can not operate or even survive on a strict vegan diet. Many of these Adom human bodies are made less than perfect and the biology is designed, as a genetically modified slave would be, as a creature that can consume whatever slop is thrown into the trough. Why would a parasite class make a slave that can naturally eat "morally"? The answer is that they wouldn't because they don't care. Their only goal is that we can consume, produce and work in order to meet their own requirements. I imagine any slave master would want their slaves to be low-maintenance. Moving on to how preaching about veganism is a distraction that takes the minds and eyes off the goal of attaining real freedom on this planet for it's inhabitants and the future. Militant vegans are pushing at the diet and telling people how evil they are for not being vegan. It is creating a group of people who are "punishing" themselves emotionally and spiritually because they ate meat for the first 20 years of their lives and now they are so EVIL and have to "make up for it" by desperately campaigning for veganism. Which leads these people to forget that people are allowed to make mistakes and change who they are as well as telling other people how evil they are because they eat meat. Not to mention a lot of vegans tend to make a full stop in their education on morality at the vegan diet information and at the "ending animal suffering" campaigns. I have actually had vegans say to me the absurd sentiment that they "have read enough and don't need to do anymore reading". As well as this, they seem to have this idea that selling people on a vegan diet will somehow, magically, get people to see the error of their ways and stop acting like dumb animals who violate the rights of others. This only creates an ill-informed and mentally chaotic personality type who can't see past the surface problems.

There are plenty of atheists, nihilists, psychopathic, parasitic, child abusers out there that will be vegan or even vegetarian and this does not change who they are fundamentally. Even people who would violate rights for one reason or another will have so-called "principles" that they will stick to for the same reasons they violate rights over. Mentally unfit people will always come up with excuses as to why they do the things that they do and there doesn't have to be a logical reason behind it. The change has to come to them at a spiritual level brought on by a physical experience that is usually in the form of a hard-lesson. And really, some people just can't be helped if they happen to have the genetically born traits that cause the underpinnings of psychopathy and then choose to act upon the impulse to violate physical rights. The only thing that can be done to help people who are naturally born psychopathic and behave as such is to humanly put them down as if they are a rabid dog. They are broken beyond repair.

The distractions that flat-earth and militant vegan propogandists push are being used as weapons against the common folk in order to divide and conquer. They are being used to muddy up the information about morality so there is nothing but miscommunication at every turn. That way perspective rules over objectivity. And this is only two examples that I could point out. And we should know by now this is a tale as old as time. Get's us every time. And it's working just as well today as is has for centuries.

Refer back the article here; "Operation Babel; The Tower of Babel and the Elohim" Link: CrossTalk! Ep. 45 The Tower of Babel and The Solution

I sometimes wonder when people are going to start feeling embarrassed for being so duped. When are people going to stop allowing themselves to be used as useful idiots in this great slavery churning machine that the parasite class gets us to operate? Can people really see the bigger picture or is it all about their own comfort because that is all they can see with their eyes? How many of us out there are actually seeing with our Minds?

We are being trained to be passive and unable to handle confrontation. On purpose. Look at our history. In the past when there was a situation where there was an over-reach of some false authority against the people there was usually the response of the people pushing back and even stopping the false authority. At least, for awhile. That is because we the people out-weigh the false authority by billions. Our numbers are great. Unfortunately, the false authority has greater influence and lots of practice in applying it.

At some point though there was a shift in this pattern and I have to ask why.

So ... why?

My theory is a cheat code was discovered. And I think it took the shape of the medical industrial complex. A vast network that is so large it is barley recognizable as a system that operates in tandem together. Working under the radar so it's not obvious as to what is happening. Using that tool of the "Unholy Feminine" and weaponizing the good faith of the people who actually care about healing the sick. A many tentacled fiend that works in the under current of our society. The healthcare system, though it may have began with all the best of intentions, has become just as corrupt and filthy as any other system that has been set in place. I would even consider that the healthcare system is the most dangerous one because no one suspects that there is ill intent at play here. An unseen predator that lurks and influences from the deepest parts of the shadows. We have an administration force in full operation. People are blinded by their fears of pain, suffering and death and so beg at the feet of the priest in the lab coat for a miracle. Which is not even something that anyone can give to begin with. The truth is that there are no quick fix's to any problem that exists. All healthcare is medical experimentation, essentially. It's finding things that work and things that don't work. Sometimes people get lucky and sometimes they don't.

Now, don't confuse healthcare with medical science. There is a difference.

Healthcare is operated by a system of administration(s) that create policies and administer treatments and drugs that are being propagated by the pharmaceutical industry. People who work in the healthcare field get incentives for falling in line with the agenda driven wants of the pharmaceutical companies.

Medical science and science in general is something else. And what doctors and scientists used to utilize before the over reach of false authority in the healthcare world that was operating with an agenda. People have forgotten that medical doctors used to be scientists as well and that was their primary job. The medical detective. They were the discoverers of the human body and what makes it tick. Science is measurable and is about discovery. Not about false authority stapling phony policies to fit an agenda.

The medical industry is a cheat code for the parasite class. As soon as we had pharmaceutical companies taking to the field and having man-made laws designed to protect them that was when this began to be a problem for the people. The pharmaceutical companies push trillions of dollars a year in drugs and treatments. Most of which cause more health problems then they actually solve and end up being more hassle then they are worth for the patient. And don't be fooled. It is always the patient who suffers for the backlash of the treatments that go wrong. The most damaging of these drugs are mood stabilizers and opiates. These drugs often lead to a deterioration of the mind and body, creating the sickness that was first diagnosed by the priest in the lab coat. Often more times than not, the patient is saddled with a drug like this at the suggestion of their "well-informed" doctor and what WAS a problem that probably could have been solved with a little honest theory turns into an actual problem in the form of mental illness or addiction. There is also the little-known fact that many of our pharmaceutical drugs have things like fluoride, arsenic and mercury in it. The excuse is that they are good for us and are used as preservatives but really these are all poisons. Poisons that are stunting our ability to function mind, body and soul. All vaccines are just as bad. And it is becoming more and more apparent that the reason why we have become so passive and ineffectual in our activities, especially when doing something about an over reach of false authority, is because we are not just being conditioned through traditional means but also being made to be docile by the drugs and treatments pushed by the pharmaceutical industry that is using doctors and scientists to influence the public.

Let's look as some history.

The United States Food and Drug Administration (FDA or US FDA) is a federal agency of the Department of Health and Human Services. They are meant to be responsible for the control and supervision of food safety, tobacco products, caffeine products, dietary supplements, prescription and over-the-counter pharmaceutical drugs (medications), vaccines, biopharmaceuticals, blood transfusions, medical devices, electromagnetic radiation emitting devices (ERED), cosmetics, animal foods & feed and veterinary products under the guise of protecting and promoting public health and safety. Their primary focus is enforcement of the Federal Food, Drug and Cosmetic Act. However, the agency also enforces laws like Section 361 of the Public Health Service Act and all associated regulations. Much of this regulatory-enforcement work is not directly related to food or drugs but involves other factors like regulating lasers, cellular phones, and condoms. In addition, the FDA takes control of diseases in the contexts varying from household pets to human sperm donated for use in assisted reproduction.

Just stop here for a moment and think about how vast that list is. Think about how much power that can give an industry to wield over a population. Each one of the subjects will have it's own branch with many facets in regards to it. They essentially own everything.

Up until recently (as in the 20th century) there was little regulation on consumable products with the exception of the Vaccine Act that was approved and regulated by the federal government in 1813 (which was repealed in 1822 after some medical malpractice incidents and the authority on how to handle vaccines were given over to the states independently). The FDA's origin story starts with the Division of Chemistry of the U.S. Department of Agriculture which was the product of the Copyright and Patent Clause. The clause, which is the basis of copyright and patent laws in the United States, states that: "{the United States Congress shall have power} To promote the Progress of Science and useful Arts, by securing for limited Times to Authors and Inventors the exclusive Right to their respective Writings and Discoveries." This gives the FDA today the rights to essentially claim ownership over all resources and consumable products.

The FDA was officially established on June 30th in 1906. That is 119 years ago. So for over a century we have an organization that has had almost full control of what we consume. The headquarters facilities are currently located in Montgomery County and Prince George's County, Maryland and is currently ran by Dr. Marty Makary (Commissioner of Food and Drugs) and Sara Brenner (Principle Deputy Commissioner). The company's jurisdiction is part of the federal government of the United States and it's parent agency is the Department of Health and Human Services. Child agencies that came from this organization is the Center of Biologics Evaluation and Research, the Center for Devices and Radiological Health, the Center for Drug Evaluation and Research, the Center for Food Safety and Applied Nutrition, the Center for Tobacco Products, the Center for Veterinary Medicine, the National Center for Toxicological Research, the Office of Criminal Investigations and the Office of Regulatory Affairs. Some of proceeding agencies that came from this organization are the Food, Drug and Insecticide Administration (July 1927 – July 1930), the Bureau of Chemistry, USDA (July 1901 – July 1927) and the Division of Chemistry, USDA (established 1862).

As a side note, as of September 9, 2025, Dr. Marty Makary is the Commissioner of the U.S. Food and Drug Administration. He was confirmed by the U.S. Senate on March 25, 2025 and is the 27th commissioner of the agency. Makary, a surgical oncologist and professor at Johns Hopkins University prior to his appointment, succeeded Dr. Robert Califf, who served two nonconsecutive terms as FDA commissioner before departing in early 2025. Makary is aligned with Health and Human Services (HHS) Secretary Robert F. Kennedy Jr.’s “Make America Healthy Again” (MAHA) agenda and has signaled a focus on rigorous scientific standards, food safety and regulatory reform.

Their research facility, White Oak Federal Research Center, is in the White Oak area of Silver Spring, Maryland and spans 130 acres where people work and live. As of 2018 the property had a population of approximately 11,000. They have two field branches which has many locations across the U.S. and internationally; the Office of Regulatory Affairs and the Office of Criminal Investigations.

The research center houses the Office of the Commissioner (OC), the Office of Regulatory Affairs (ORA), the Center for Drug Evaluation and Research (CDER), the Center for Devices and Radiological Health (CDRH), the Center for Biologics Evaluation and Research (CBER) and offices for the Center for Veterinary Medicine (CVM). I invite you, the reader, to look into what these facilities actually do. Essentially, they have the power to regulate all consumable products from here.

The field Office of Regulatory Affairs (OCA) is the "eyes and ears" of this operation and this is the branch that investigates everything that is operating within and outside the FDA's control. The agents are called Consumer Safety Officers. They investigate production, warehousing facilities, complaints, illnesses or outbreaks and review documentation in the case of medical devices, drugs, biological products and other items where it may be difficult to conduct a physical examination or take a physical sample of the product. They are the watch dogs of the FDA and wield the power to make or break any company depending on what they say to the "authority" on the matter.

The field Office of Criminal Investigations (OCI), which was not established until 1991, was created to investigate criminal cases. They are armed and have badges that give them the "authority" to decide who is violating the federal laws and who is not. They are the street thug enforcers of the FDA. This branch works hand in hand with the Federal Bureau of Investigation (FBI), assistant attorney general, Interpol and OCA.

It's also the FDA that has the say-so on emergency protocols. Such as the Emergency Use Authorization (EUA) policy that was established to facilitate the availability and use of medical countermeasures, including the use of all vaccines and personal protective equipment, during public health "emergencies". This policy was sandwiched in through the Project BioShield Act (established in 2001) in 2004. This legislation amended Section 564 of the Federal Food, Drug and Cosmetic Act to allow the U.S. Food and Drug Administration (FDA) to authorize the emergency use of unapproved medical products or unapproved uses of approved products (Medical countermeasures (MCMs) operated by a federal program called "FDA Medical Countermeasures Initiative" (MCMi)) during declared emergencies involving chemical, biological, radiological or nuclear threats. Their is an online "black list" which names dozens of branded drug companies that are supposedly using unlawful or unethical means that attempt to impede competition from generic drug companies. I would be curious to find out how many of these are actually dangerous and how many are just companies that use natural based treatments.

When it comes to actual food and dietary supplements the FDA is loosely governed by a set of statues that was approved by the United States Congress but are interpreted by the administration of the FDA. Meaning they can take it as they see fit in order to meet their own agenda. It is under the Dietary Supplement Health and Education Act of 1994 (DSHEA), that the FDA can enforce that manufacturers and distributors of dietary supplements and dietary ingredients meet the "current" requirements that only the FDA approves of.

The FDA has the power to regulate almost every facet of prescription and non-prescription drugs, including testing, manufacturing, labeling, advertising, marketing, efficacy and safety. They are the final word on it. In 2018 they released a statement regarding new guidelines to help food and drug manufacturers "implement protections against potential attacks on the U.S. food supply" which you could really label almost anything as such. They also use tactics of regulatory shaming through online publication of non-compliance, warning letters and "shaming lists." Regulation by shaming harnesses the companies sensitivity to reputational damage.

Someone should be asking why these people own everything and why are they ALL operated under the FDA and with the full authority of the federal government.

Let's look at an example of how the FDA has abused this power that they wield over all our resources. Charges of corruption first emerged in 1988 (under the presidency of Ronald Reagan) during a congressional investigation into the FDA's activities. In 1989 their was a scandal involving the procedures that the FDA uses in order to approve generic drugs for sale to the public. The complaint brought against the FDA by Mylan Laboratories Inc. under discrimination violations. They had launched their own investigation into the FDA after they had repeated delays of their application to manufacture generic products. What were the delays about, exactly? If Mylan Laboratories were not following the guidelines why not just reject the application rather than stall it? Eventually the company filed a lawsuit against two former FDA employees and four drug-manufacturing companies, charging that corruption within the federal agency resulted in racketeering and in violations of the antitrust law. Mylan states, "The order in which new generic drugs were approved was set by the FDA employees even before drug manufacturers submitted applications" and that this was being used in order to give preferential treatment to certain companies. In 1989, three FDA officials, Charles Y. Chang, David J. Brancato and Walter Kletch, pleaded guilty to criminal charges of accepting bribes from generic drugs makers and two companies (Par Pharmaceutical and its subsidiary Quad Pharmaceuticals) pleaded guilty to giving bribes.

Before the FDA there was a vast amount of goods that people could have bought over the counter, many of the products containing harmful elements like morphine, heroin and cocaine or being outright fraudulent. There was a major turning point when the book "The Jungle" written by Upton Sinclair in 1906 which revealed unhygienic conditions in the meatpacking industry and widespread press coverage of unsafe drugs. Spurred on by public outrage Congress passed the Pure Food and Drug Act of 1906, which was meant to stop the interstate sale of misbranded or adulterated food and drugs. This was the first step that led to the inception of the FDA as we know it.

The FDA's roots are in the U.S. Department of Agriculture’s Division of Chemistry (renamed in 1930 the Bureau of Chemistry) and led by Harvey Washington Wiley who is considered to be the "father of the FDA".

There are 223 field offices and 13 laboratories located across the 50 states, the United States Virgin Islands and Puerto Rico. In 2008, the FDA began to post employees to foreign countries which included China, India, Costa Rica, Chile, Belgium and the United Kingdom. One of the programs they operate under is the Emergency Use Authorization (EUA) policy which we have now learned is a mechanism that was created to facilitate the availability and use of medical countermeasures, including vaccines and personal protective equipment, during public health emergencies such as the Zika virus epidemic, the Ebola virus epidemic and the COVID-19 pandemic.

Is it starting to make more sense now? They own everything and they can do just about anything. The FDA and establishments like it are nothing more than the state approved versions of the "snake-oil sales man" and the people, being easily taken for a fool, bought this idea that we needed to regulate what people consume. Our beautiful planet doesn't have a problem with government over reach dictating our freedom of autonomy. It's, in fact, the other way around. It has a problem with medical control over reach that is using the government in order to control and enslave the human population on this planet. And things like the FDA is just one of those means. Institutions like the FDA are always working on expansion.

The FDA uses what is called a "user fee" in order to collect payment from pharmaceutical, biotechnology and medical device companies when they submit applications asking for approval to market new products. The purpose of user fees is to provide the FDA with a dedicated financial source in order to review of new drug, device, generic and biosimilar applications and is a supplement income to the money that they get from Congress. This is essentially how the FDA stays in operation. All companies that have something to do with any of the operations that we listed above pay the FDA to review & approve their products, regardless of if it is safe or not.

The initial purpose of the FDA is meant to have been an objective "middle-man". The idea is that the review is meant to determine if it is safe but we are living in a world that is compromised by people who have nefarious intentions. Up to this point we have a corrupted system that is using the FDA to control all the consumable products in this country.

The process began with the original Prescription Drug User Fee Act (PDUFA) in 1992 which was the first of many laws to follow. Congress has reauthorized the PDUFA and all other FDA acts that were established afterwards every five years; 1997 (FDAMA), 2002 (MDUFMA), 2007 (FDAAA), 2012 (FDASIA) and 2017 (FDARA).

As a side note, the president of United States in 1992 was George H. W. Bush. It is historically well documented that the Bush family have always been a consumable product trafficking family that goes back many decades at least, if not centuries. The FDA is just another way to facilitate the trafficking of any consumable product.

The FDA may have been just another "well meaning" organizations that was started in order to keep the people safe from grifters and quack doctors, but like all organizations and institutions that get wrapped up in any governmental (or should I say, parasitic) affairs then it is soon to become infiltrated by people who use it to control the population. If they produce all the consumable products, essentially all of our resources that we require, they can dictate what and how we use any product that is produced. Since 1992 the FDA has been a tool for control and is used as a bribing system in order to get consumables produced for public consumption with very little interference or without any outside influence or oversight. All operations were kept inhouse and so could be controlled fully by whoever is currently in charge.

In 2017 the FDA Reauthorization Act (Public Law No. 115-52) was established by U.S. President Donald J. Trump. It is a the last one reestablished in a long line of "user fee" acts that began in 1992 with the Prescription Drug User Fee Act. This is a U.S. federal law that reauthorized and amended some of the key user fee programs for the FDA that covered the Prescription Drug User Fee Act (PDUFA), Medical Device User Fee Amendments (MDUFA), Generic Drug User Fee Amendments (GDUFA) and Biosimilars User Fee Amendments (BsUFA). The supposed idea was to introduce measures to improve drug development, generic drug access, medical device oversight and post-market drug safety monitoring. It's a law that is meant to give faster access to new treatments by streamlining FDA review and approval processes and enhances patient safety initiatives, such as the FDA’s Sentinel Initiative for monitoring medical product safety post-approval and encourages greater patient involvement in drug development.

So what does that mean?

Even though not everything was altered, there are some key differences between the 2012 version of the FDARA and the 2017 version. Both acts reauthorized programs for prescription drugs, medical devices and biosimilars. The 2012 act introduced the Generic Drug User Fee Amendments (GDUFA I). In 2017 the GDUFA II was implemented with a new, streamlined fee structure and made substantial updates across programs. It also increased the total revenue amounts and base fees for fiscal years 2018–2022. The GDUFA II restructured generic user fees, moving from facility-based fees to Abbreviated New Drug Application (ANDA)/Drug Master File (DMF) application fees that aimed for accountable regulation. Specifically, the FDARA act reformed the generic drug access and approval speed, including provisions to expedite the approval of generics with limited competition, enhanced device inspection and regulatory improvements for medical devices, expanded pediatric drug and device provision and new provisions to streamline drug and device review, including more frequent communication between FDA and applicants as well as public reporting on review timelines. It also puts focus on tackling the backlog and increasing generic drug competition with the intention to lower drug costs for patients and mandated transparency in FDA's review process and communication with manufacturers. This FDA is no longer "legally" allowed to hide behind closed doors.

So essentially the 2017 act did something that no other act had done. It increased the user fees that companies have to pay to get their product reviewed (making it more of a priority to summit a product that will not have any negative financial backlash later and put them in a negative spotlight potentially costing them billons), streamlined the fee structure (so people aren't waiting for years) and prioritizing generic approvals (so the general public could get a product for very cheap), highlighted and improved the device regulations approval process and forced transparency and communications between them and the general public (which means that the FDA can no longer keep their operations "in-house"). This would certainly put a wrench in the works of the FDA and hinder their ability to do whatever they want. Such as fully taking control of a population over a fake pandemic under the Emergency Use Authorization policy.

The launch of federal investigations on pharmaceutical companies would have never taken place over what is causing the rampant and ever rising causes of children with disabilities if this was not the case seemingly since 1988.

It's the little details that matter.

Now, let's be clear. If I were the one with the final say on things I would say the FDA should be dismantled in full and done away with completely. But let's be real, the vast majority of the people on this planet, firstly does not know how dangerous and powerful the FDA really is and secondly does not know how to function in a world without institutions telling them how to live their lives. We are not living in an adult world. We are living in a world where "babysitters" were established in order to regulate how all aspects of life operate, including those aspects of freewill and personal choice. We have a parasite class that is using all the useful suckers to manage this.

What is interesting to consider is that now knowing this little bit of history and then the conclusion of what Trump did in 2017 while also now seeing some effects take place in the medical world, both from personal experiences dealing with the medical realm and from what is happening at the federal level, this is pointing out to me that things are not what they seem to be. It is not business as usual.

I would suggest that people keep their minds open and reserve their full judgment until everything shakes out. Investigate all the information, not just whatever fits your own current viewpoints that you might constitute as proof. Be the real investigative detective and be wise enough to discern the little details because that is usually were you will find all the changes that take place are. Hiding deep in the shadows.

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