The medical industrial complex and scientistic cult evidently keep using the most vulnerable members of society (especially children) as a sacrifice in the pursuit of their efforts. But, with all that we know about the medical industrial complex, this is not news to anyone. In fact, what is expected is that there be progressive institutional reform in the status quo – especially in the second Trump administration – that directly challenges these issues. However, what is being exposed is just how deeply entrenched regulatory bodies are in their collusion with the medical industrial complex – especially pharmaceutical companies. But, today, we ought to discuss this further in light of Moderna’s mRNA COVID Shot getting Full FDA Approval for said to be “At-Risk” Infants.

U.S PRESIDENT DONALD TRUMP THREATENS 35% TARIFFS ON CANADA STARTING AUG. 1

U.S President Donald Trump has threatened a 35% tariff on goods imported from Canada. [ROLL CLIP00:11-] Trump’s announcement of higher tariffs on Canada comes amid a flurry of letters the U.S President has sent to world leaders over the past week informing them what rates their goods will be tariffed at come August 1, absent any trade deals.

BRAZIL VOWS RETALIATORY TARIFFS AGAINST US IF TRUMP FOLLOWS THROUGH ON 50% IMPORT TAXES

In a related matter, Brazilian President Luiz Inácio Lula da Silva has said that he will impose retaliatory tariffs on the United States if President Donald Trump follows through on a pledge to boost import taxes by 50% over the South American country’s criminal trial against his predecessor, Jair Bolsonaro. Lula said he will trigger Brazil’s reciprocity law approved by Congress earlier this year if negotiations with the U.S. fail.

NETANYAHU SAYS HOPING HOSTAGE DEAL WILL BE FINALIZED ‘IN A FEW DAYS’

On the last day of his 4-day trip to the US, Benjamin Netanyahu released a brief clip detailing his discussions with US President Donald Trump as well as Israel’s plans for Gaza amid ceasefire talks. Netanyahu emphasised Israel’s previous goals in Gaza including the removal of Hamas, demilitarisation of Gaza.

UK, FRANCE ANNOUNCE AGREEMENT ON PILOT MIGRANT RETURNS PROGRAM

British Prime Minister Keir Starmer and French President Emmanuel Macron have reached an agreement on a pilot programme to return migrants and refugees arriving in small boats, in a scheme to curb crossings over the English Channel. In a joint press conference on Thursday, Starmer said people arriving in the United Kingdom on small boats will “be detained and returned to France in short order”.

MODERNA’S mRNA COVID SHOT GETS FULL FDA APPROVAL FOR “AT-RISK” INFANTS

On July 10, 2025, the FDA granted full approval for Moderna’s mRNA COVID-19 vaccine (Spikevax) in “at-risk” children aged 6 months to 11 years. The shot was previously available only under emergency use authorization. This approval comes despite a mountain of evidence linking the shots to catastrophic harms, some of which include heart damage, brain damage, cancer, and mass death. Once again, this decision is quite concerning as it shows that regulatory agencies remain captured by the Bio-Pharmaceutical Complex. And so, one has to ask: How many more children must be sacrificed before accountability begins?

THIS MOVE COMPOUNDS THE LACK OF TRUST TOWARDS THE FDA

Now, this move certainly compounds the lack of trust towards the FDA, and necessarily so when you consider who influences the policy direction of the FDA. The general points of historical context to note regarding the FDA is that it was established in 1906 in response to public concern over unsafe food and drugs, such as spoiled food and counterfeit products. However, food industry lobbyists gradually gained influence, leading to the removal of the agency’s original leader. As a result, numerous harmful food additives were granted “generally recognised as safe” (GRAS) status and continue to be used today.

Then, in 1962, the FDA was given broad powers to oversee drug safety following the thalidomide incident. Unfortunately, the new regulations created strict standards for drug efficacy that were often selectively enforced, benefiting the pharmaceutical industry. Unfortunately, the FDA then increasingly targeted natural therapies, which led to many being erased from history – all of which is incredibly important to remember in light of our subsequent discussion on the propaganda against salt. Nevertheless, this historical context is why – despite the numerous attempts to reform the agency – issues of inefficiency and bias within the FDA persist. [PAUSE]

Now, evidence of the lobbyist factor in the FDA’s work, can be inferred in the agency’s work in food regulation. For instance, in the late 1800s, food producers were selling adulterated products, and pharmaceutical companies peddled medicines with secret ingredients like opium and alcohol. Public outrage grew, especially after exposés like Upton Sinclair’s ‘The Jungle’, which helped spark the 1906 Pure Food and Drug Act. This law gave the Bureau of Chemistry the power to ensure accurate labeling and prevent harmful additives in food.

Well, the director of the Bureau of Chemistry (and thus the first head of the FDA), Harvey Wiley conducted tests on food additives, proving they made healthy volunteers sick. While the public and many scientists supported his findings, the food industry fought back with powerful lobbyists and legal tactics. Well, Wiley’s book “The History of A Crime Against The Food Law” went on to detail much of the same abhorrent industry tactics we see happening now. But, this is all to detail the contextual background behind the FDA’s propensity to be influenced by lobbyists from the industries it is supposed to regulate – which is the first aspect of the FDA’s problem with corruption.

THE FDA’S DECEPTIVE AND HARMFUL “GENERALLY RECOGNISED AS SAFE” STATUS

Let’s then proceed to discuss the FDA’s “Generally Recognised as Safe” status. Many food additives are “generally recognised as safe” (or GRAS), and what this actually means is that they are widely used but WITHOUT REGULATION! Well, GRAS food products presented two fundamental issues: food industry counterfeiting and harmful additives. More specifically, the industry often fakes products to cut costs; for instance honey is often faked by adding cheap syrups or other ingredients to mimic its appearance and taste; while polluted waters are also added to enlarge oysters.

Now, despite evidence of harm, the food industry claimed these additives were essential for production, even though competitors showed higher-quality (and ultimately more profitable) products could be made without them. However, there were warnings that chronic exposure to additives could cause long-term health issues, such as organ damage; and these warnings were ignored – especially as the influence of industry lobbyists grew – which is why these harmful additives and faked foods were eventually reclassified as “generally recognized as safe.” But of course, these so-called “safe” additives have contributed to widespread chronic illness in society. Here’s more on the FDA’s GRAS status.

Furthermore, companies currently self-certify their chemicals without independent oversight; which has resulted in ingredients like titanium dioxide – which is banned in Europe and other developed nations still being legal in the US despite mounting health concerns. Through GRAS, FDA has for the longest time applied an “innocent until proven guilty” approach to food! Which is a categorically dangerous approach; ingredients should not have to harm or kill people first before they are deemed unsafe!

PETER MARKS AND THE FDA’S COVER-UP OF THE HARMS OF COVID JABS

Let’s also look at vaccine cover-ups, as being part of the reasons behind the compounding lack of trust towards the FDA. Many have been horrified to learn that the FDA and CDC systematically ignored every possible sign the COVID vaccines were dangerous as they pushed it on more and more people. One of the ways people were made aware of this was through the recently leaked recordings showing how stubbornly the head of FDA’s vaccine division, being Peter Marks at the time, refused to acknowledge any of the evidence brought forward by a group of permanently injured vaccine recipients, and even medical practitioners who were treating vaccine injured patients.

Here’s why this is important to note: generally, in looking through what transpired with the COVID-19 response, Anthony Fauci is commonly blamed for all that went amiss – and correctly so. However, we must not also miss the people who were also directly involved, while hidden within the FDA bureaucracy. One such person is Peter Marks. Peter Marks is the primary person who covered up the reports of COVID vaccine injuries (and instead repeatedly told the world they were (quote unquote) “safe and effective”). He was also the person who kept on pushing the FDA’s chief vaccine scientists (who were very pro-vaccine) to accelerate and condense the approval timelines for the COVID jabs (as those approvals were needed to legally implement Biden’s vaccine and booster mandates). The parties involved in this process, which included, Marion Gruber and Philip Krause (who were the Director and Deputy Director of the FDA’s Office of Vaccines Research and Review, respectively); they reported that there were (at that point) no more corners they could cut to further accelerate the COVID vaccine approvals, at which point they were removed from the COVID vaccine approval process and Peter Marks took it over (at which point the unjustifiable approvals and mandates quickly followed).

THE PROBLEMS WITH THE FDA ARE FURTHER ENABLES BY STANDARDS IN MEDICINE

So, while the FDA is central to focus on as far as recent developments are concerned, it’s important also to note that the problems with the FDA are FURTHER enabled by standards in medicine. And I say that because it occurred to me that even if we have bad regulators who approve bad medicine, if we had good doctors and medical standards, then the harms could easily be averted or mitigated. But if the medical standard is overmedication and trusting “the science”, while doctors function as pharmaceutical representatives, then of course the problems are worse.

Let’s look at medical education. No matter how you dice it, medical education is quite challenging as there is simply too much to learn, and so even the “brightest” students adopt a triage mentality where they cut out things that NOTt necessary (or low-yield) (specifically) for exams so they can pass and get a degree. And because of this medical education typically presents 3 issues as far as medical standards are concerned.

First, the present standard of medical education covers many aspects in a superficial manner (e.g., med students just learn the classic indications, simple mechanisms of action and commonly recognized side effects of drugs). Now, this is quite problematic as many of those simplistic facts students memorize aren’t always entirely correct (or become evidently contradictory once you take the time to understand them). However, since students are under such pressure to memorize them, they take the facts as verbatim facts they don’t question and become quite haughty towards those who do.

Second, there has been a strong focus in medicine on the key medical products on the market (e.g., doctors focus on how to use pharmaceutical drugs along with the key microbes and their pharmaceutical treatments, understanding what aspects of the body each speciality is responsible for, how to interpret imaging studies, and even how to understand surgery well enough to want to go into it or refer patients to it). Similarly, there is also a strong focus on just the basic skills necessary for being a doctor (this includes being able to recognize potentially life-threatening conditions, conducting a physical exam with enough details to complete a medical note and writing billable medical notes). That said, there is also (thankfully) a strong focus on anatomy and physiology, which along with recognising key diseases and medical emergencies, represent some of the most valuable aspects of conventional medical training.

Then the third issue presented as far as medical standards are concerned has to do with how medical training cuts out a lot of the subtle aspects of medical science and doctoring that make you an effective clinician (and this includes things like medical ethics). And because of this, there is always a subset of medical students who have that inherent capacity and excel at being clinicians but very few learn it through their training. Put differently, standard medical training does NOT really cover what is needed to make people healthy as there is never enough time for that and again and again, we hear stories of medical educators who try to incorporate it but get pushed to the side due to limited curriculum time.

So, in a world where medical standards prioritise pharmaceutical interventions, and medical education and training focuses purely on passing exams as opposed to being more concerned with aspects of medical science that make a med student an effective clinician, well then of course the FDA’s corruption will have crippling impact, because doctors themselves are trained to push what the FDA has approved.

Well, no wonder the medical industrial complex is so-multilayered. There are clearly various actors involved. But, this also gives broader context behind why doctors become progressively less focused at making their patients better, while becoming product pushers for the pharmaceutical industry. Take this testimony from a pharmaceutical representative of 32 years. She exposes the corrupt relationship between big pharma and doctors, primarily based on greed because it was about organising expensive gifts and experiences for doctors in exchange for their product loyalty.

WORST OF ALL IS THAT PATIENTS ARE DISADVANTAGED BY THE MEDICAL SYSTEMS

I’ve had discussions with medical students and practitioners on the necessity of strict standards to enter medicine because it is one of those fields where there is no room for error. ANd I think many people still have that same perception of the medical field: which is that it brings in the best and trains them rigorously so they are less susceptible to making mistakes that can be the difference between life and death for some. BUT… while there absolutely are exceptions who are incredible doctors, it is also clear that the medical system is not as fool, corruption, and greed-proof as we thought. And worse of all is that there are many people who have not broken free from this presumption of excellence and efficacy in the medical field, and pay with their lives. And yet, the issues in medicine are quite nuanced because it is NOT just the FDA that has been financially bought out – it is almost everyone, down to the medical schools that teach the doctors that are supposed to practise evidence based and holistic medicine. In fact, the verdict from good doctors is that there is almost no such thing as evidence-based medicine anymore, in a world where big pharma has gained influence over regulators and academia.

Written By Lindokuhle Mabaso

And now onto our main discussion regarding Dr Robert Malone; and the War Against the Medical Industrial Complex; and we ought to start with the latest development; which is that the HHS Secretary, being Robert F. Kennedy Jr, has appointed Dr Robert Malone to the Advisory Committee for Immunisation Practices. You’d recall that in the previous weeks, the secretary had fired all 17 members of the Center for Disease Control and Prevention’s (CDC) advisory committee for immunization practices (ACIP) – which is a group of alleged scientific experts who recommend how vaccines should be administered and distributed.

In an op-ed published in the Wall Street Journal, Kennedy stated that (quote): “The committee has been plagued with persistent conflicts of interest and has become little more than a rubber stamp for any vaccine. It has never recommended against a vaccine—even those later withdrawn for safety reasons. It has failed to scrutinize vaccine products given to babies and pregnant women. To make matters worse, the groups that inform ACIP meet behind closed doors, violating the legal and ethical principle of transparency crucial to maintaining public trust.”.

Well, the 17-member ACIP panel was scheduled to meet later in the month of June to review recommendations, including those involving COVID-19 vaccinations for children. That meeting will still go ahead, but without the current panelists, some of whom Kennedy said were ‘last-minute Biden appointees’ whose terms would have otherwise extended until 2028.

So, on the one hand, those supporting this move say this is exactly the kind of bold move needed to break the credibility crisis surrounding vaccine science and government health agencies. This is especially considering that Secretary Kennedy remarked that the new appointees won’t directly work for the vaccine industry” and will “refuse to serve as a rubber stamp,” instead fostering “a culture of critical inquiry”. But, on the other hand, those against this decision argue the opposite, insisting that the move reeks of ideology and raises concerns that Kennedy will stack the committee with vaccine skeptics or unqualified appointees, thus further eroding trust – and you typically heard this argument from Democrat officials, such as Senate Minority Leader Chuck Schumer and Senator Bill Cassidy; and the liberal media.

PUBLIC TRUST IN THE HEALTH CARE SYSTEM WAS ALREADY ON A STEADY DECLINE

Now, during the period that Secretary Kennedy fired those committee members, a number of media houses and publications reported that the immediate concern for public health officials, scientists and vaccine researchers was both the erosion in trust AND who will fill the newly opened seats. Let;s address the public trust issue first. In essence, here is what was ignored by the critics and skeptics: the erosion of trust in the public health system FAR pre-dates the firing of all 17 members of the Center for Disease Control and Prevention’s advisory committee for immunization practices! The erosion of trust occurred because patients have long been bearing the brunt of a corrupt medical system that puts them in debt (at times even rendering them homeless), through charging them for insanely expensive and unnecessary procedures, tests, and medication. Public trust was eroded by doctors and nurses who were murdering patients and getting away with it because of the lack of adequate oversight in the medical industry.

Trust further eroded when mothers were dying at alarming rates after giving birth in first world countries. And eroded even more when the COVID debacle was exposed, and pro-vaccine individuals were being gaslit when reporting vaccine injuries. But, worse of all, this erosion erupted because people discovered that the regulatory bodies that were supposed to hold pharmaceutical and medical corporations accountable had a revolving door relationship with the entities they were supposed to keep from doing any harm. In fact, even the CDC was reporting a fall in vaccine rates by 2024. More specifically, a Centers for Disease Control report titled, “Influenza, COVID-19, and Respiratory Syncytial Virus Vaccination Coverage Among Adults — United States, Fall 2024”, found that, by November 9, 2024, only an estimated 17.9% of adults aged 18 years or above had received the updated COVID-19 booster injection. But, ultimately, these failures of the public health system are where the public trust problem emanates from.

And in light of this (and also responding to the claim that this change reeks of ideology) I’d like to point out that the issues resulting in the erosion of public trust in the medical system that we’ve just outlined – they took place in Democrat administrations as well (in fact more, when considering that America has largely been under Democrat leadership more times than Republican). Therefore, if this measure strengthens accountability by removing people with conflicts of interest, and does this in a field of medicine that has become incredibly controversial – it sounds like the problem is being addressed and not exacerbated.

Secondly, what would be a careless exacerbation of the problem with a lack of public trust is keeping a status quo where public trust is already eroded. Therefore, responding by removing people who have been complicit in the creation and keeping of the problem seems like a fairly sensible thing to do. But, here’s more on how public trust in the health care system was long on a steady decline; including a concession from officials of the CDC and NIH during the Biden Harris administration on their role in decreasing public trust.

Now, I find it interesting that each of the officials we just watched highlighted the need for better transparency in their respective agencies – which sounds like exactly what Secretary Keneddy was advocating for in firing people who had a conflict of interest, while simply rubber stamping vaccines without much enquiry or transparency. But, of course, those officials never actually lived up to their words about transparency, following their concessions in 2024 on how their respective agencies fuelled public distrust. Additional proof of this is the fact that the concession excerpt we just watched followed another meeting in 2023, where Rep. Mariannette Miller-Meeks (R-IA) questioned witnesses about school reopening procedures during the pandemic at a House Energy Committee hearing on “Assessing the CDC’s failures in fulfilling its mission”.

Well, it sounds like the CDC has long had issues with public trust. And removing members of an advisory committee in the CDC that is riddled with a conflict of interest, is a necessary response. Now, there is also the media aspect in this – in particular the publications and media houses that were (quote unquote) raising the alarm about this shift in the advisory committee. It’s really simple: the medical industrial complex funds a significant portion of the media, and has made them into their media intermediary, responsible for spreading and the proselytising of a polluted science. The COVID-19 period has shown a very high level of scientific censorship, causing many people difficulties to access relevant health information. Moreover, the pharmaceutical industries are known for their propaganda in favour of the disease. Pharmaceutical industries are known to provide inaccurate and misleading promotional information about their medicines, but also inaccurate information on diseases and disease risks, which can lead to unnecessary medication and induce side effects caused by these medicines. They pay government officials and even medical practitioners to keep themselves from being exposed. But, evidently, they also capture the mainstream media through advertising revenue, which allows them to regulate what is said about pharmaceutical products.

DR ROBERT MALONE APPOINTED TO ADVISORY COMMITTEE FOR IMMUNISATION PRACTICES

Well, we mentioned earlier that in addition to the claimed issue of a decrease in public trust, critics also expressed concern about who would replace the dismissed advisory committee members. This was a question that was quickly answered as Secretary Kennedy has also announced the new members making up the ACIP panel. These members include Drs: Robert W Malone; Martin Kulldorff (who was a co-author of the Great Barrington Declaration, along with Dr Jay Bhattacharya, who is president Trump’s pick for the director of the National Institutes of Health); there is also Cody Meissner (and he is a professor of pediatrics at the School of Medicine at Dartmouth. He previously held advisory roles at the FDA and CDC, including ACIP from 2008-2012. In 2021, Meissner co-wrote an editorial with Dr Marty Makary, who is now the head of the FDA, which criticised mask mandates for children).

Also named in the advisory committee is Vicky Pebsworth (Pebsworth is a nurse and the former consumer representative on the FDA’s vaccine advisory committee. She is also the Pacific regional director for the National Association of Catholic Nurses). Fifth on the committee is Retsef Levi (Levi is a professor of operations management at the MIT Sloan School of Management who Kennedy described as an “expert in healthcare analytics, risk management and vaccine safety). Then there is Michael A. Ross (Clinical Professor of Obstetrics and Gynecology at George Washington University and Virginia Commonwealth University, with a career spanning clinical medicine, research, and public health policy). Seventh in Joseph R. Hibbeln (who is a California-based psychiatrist who previously served as acting chief for the section of nutritional neurosciences at the NIH); and finally is Dr James Pagano (who is an emergency medicine physician from Los Angeles “with over 40 years of clinical experience”, and a “strong advocate for evidence-based medicine).

Now, one of the most notable names is Dr Robert Malone, who is a biochemist who made early innovations in the field of messenger RNA but in more recent years has been a vocal critic of mRNA technology in Covid-19 vaccines. His announcement has made those in support of the medical industrial complex run amok. As such, they have responded with instant, coordinated character assassination efforts and desperate attempts to erase his record. Their terror is quite palpable!

WHY THE MEDICAL-INDUSTRIAL COMPLEX OPPOSES DR ROBERT MALONE

Once again, the backers of the medical industrial complex have responded to Dr Maone’s appointment with instant, coordinated character assassination efforts and desperate attempts to erase his record – because they are concerned about what this appointment means for their nefarious plans. Well, they should be concerned. Dr Robert Malone is particularly equipped to dismantle this collection of corrupt systems and subsystems from the inside, thus the wisely alarmed position of the opposition on large horse statue gifts from the Trojans. Afterall, they don’t attack nobodies. They don’t coordinate against empty suits. They target people who threaten the machinery.

What is interesting about Dr Malone is that he was never inherently interested in public office – much like Donald Trump in his early career as a businessman. In the case of Dr Robert Malone, he is regarded as someone driven by a moral imperative that compels him to serve and to do it outside of politics, especially seeing he had already suffered through that crucible during Covid crackdown on dissenting doctors; and thus knew the political terrain. And so he has preferred working with states or private partners, where bureaucratic constraints would not muzzle urgent action. And so, he did not seek a federal appointment, but when Kennedy asked him – with the moral urgency of a country in collapse – Malone chose service over safety.

In any case, Dr Malone’s appointment triggered a predictable media offensive, laced with insinuation and omission. Major outlets, operating in lockstep, flooded the digital landscape with headlines crafted to imply fraud without making refutable claims. Phrases like “played an early role in mRNA development…” and “claims to have invented…” flooded mainstream media discussions. And they did this in an effort to plant seeds of doubt without offering substance – which is a classic psyop strategy.

But, let’s make this plain: the establishment isn’t reacting this way because Dr. Malone lacks credibility. They’re reacting this way because he threatens everything upon which they rely to maintain control. This is to say that: Dr Malone isn’t just a critic of captured science – he helped build the scaffolding of modern molecular medicine. He holds dozens of issued patents, including foundational work in mRNA and DNA vaccine platforms. He understands the system from the inside out – its science, its politics, its regulatory gamesmanship. And now he’s turned that knowledge toward exposing and repairing the institutional rot that has poisoned public health policy.

For instance, Dr Robert Malone in 2022, warned parents about the contents of mRNA technology – at a time when only a few voices such as the president of loveworld Incorporated were at the forefront of exposing the dangers of mRNA technology. In addition, Dr Robert Malone also exposed the “military-grade psychological operation” otherwise known as the “Covid-19 pandemic”. He has publicised how Western governments, non-governmental organisations, transnational organisations, pharmaceutical industry corporations, media and financial corporations have co-operated via public-private partnerships—which he calls a euphemism for fascism—to deploy the most massive, globally harmonised psychological and propaganda operation in the history of the world.

Written By Lindokuhle Mabaso