Once labeled a dangerous ‘anti-vax’ technique, head of the FDA’s Center for Biologics Evaluation and Research, Dr. Peter Marks is now stating he would space out vaccines to avoid mounting adverse reactions.
I would like to open this column by stating that I have long had a great relationship with Amazon, which has sold far more of my books than have ever been sold in bookstores. I have also been extremely grateful to Amazon’s Kindle Direct Publishing program for empowering me to publish whatever nonfiction books I please, quickly and efficiently, while retaining the rights and earning the best royalty in the business.
In May 2022, Dr. McCullough and I published our book, The Courage to Face COVID-19: Preventing Hospitalization and Death While Battling the Bio-Pharmaceutical Complex, directly on Amazon. Quickly the book became a hit and within a year it had earned over 1000 5-Star Reviews. For almost 3 weeks in July 2022 it was a top 100 seller.
In the autumn of last year, Tony Lyons, President and Publisher of SKYHORSE in New York, graciously offered to bring out a special, handsome hardcover edition with a preface by U.S. presidential candidate, Robert F. Kennedy, Jr., who warmly endorsed our work.
A bit of Covid fatigue this year caused sales to decline, but in September the book got a second wind as more and more Americans seem to be recognize that Dr. McCullough has been right all along.
To my gratitude and delight, Amazon actually supported the effort by running a deep discount promotion while still paying the same royalty to us—an act of generosity to authors that is unheard of in traditional publishing.
And then, on September 29, seemingly out of nowhere, Amazon Account Review sent me the following notice:
We have temporarily suspended your KDP account because we found offensive content that violates our Content Guidelines in the title(s) listed below:
ASIN: B09ZLVWMD9 –
Title: THE COURAGE TO FACE COVID-19: Preventing Hospitalization and Death While Battling the Bio-Pharmaceutical Complex – Author: John Leake
Upon receiving this message, I humbly beseeched Account Review to restore my account and to let me know what “offensive content” was found in our book. Amazon restored my account and published my latest book—a conventional work of true crime—but refused to reinstate The Courage to Face COVID-19. Yesterday my third appeal was turned down without answering my query about what in our book is offensive.
My question seemed especially pertinent, given that Account Review provided me with a link to its Content Guidelines, which include a section on Offensive Content.
Offensive content
We don’t sell certain content including content that we determine is hate speech, promotes the abuse or sexual exploitation of children, contains pornography, glorifies rape or pedophilia, advocates terrorism, or other material we deem inappropriate or offensive.
Obviously, nothing in our book even remotely touches on any of these subjects. Upon reading this description, it occurred to me that it was a perfection description of 120 Days of Sodom, by the Marquis de Sade, which contains hundreds of pages that glorify the abuse and sexual exploitation of children, violent pornography, and glorifications of rape and pedophilia. I did a quick search for the title, and voila, there it is, for sale on Amazon in three formats.
None of my polite entreaties to Content Review was answered with an explanation of what, in our book, is offensive or in violation of any other published guideline. This strengthened my suspicion that the decision was the result of a sudden imposition of power for which the Content Review staff was not prepared.
Even more stunning than banning my softcover edition was Amazon’s decision to ban Tony Lyons’s SKYHORSE hardcover edition from the site without even sending the publisher notice. He learned of his edition’s demise from me.
This is a developing story about arbitrary censorship and book banning. Generally speaking, Amazon has a robust history of resisting pressure to ban books. Even during the COVID Pandemic, Amazon bucked the censorship regime that was established at Facebook, YouTube, and Twitter.
I believe it is no exaggeration to state that Amazon’s decision to ban our work of medical and historical scholarship, carefully vetted by Dr. Peter McCullough—who has published over 600 peer-reviewed papers in top academic medical journals—is the most egregious act of arbitrary censorship in the history of American publishing.
Many works of literature have been banned from public school systems and libraries and censured by religious organizations. However, I cannot find a single example of a banned nonfiction book that contains zero sex, zero violence, zero expletives, zero harshly expressed opinions, and zero assertions that aren’t grounded on rock solid scholarship.
Indeed, the book is a strictly factual narrative based on hundreds of published sources ranging from academic papers to standard works of medical history to documents published by U.S. federal agencies. The longest chapter in the book recounts Dr. McCullough’s U.S. Senate testimony on November 19, 2020.
This is a developing story about a gross infringement of the freedom of speech that is enshrined in the First Amendment of the U.S Constitution. Coincidentally, tomorrow (October 10) I have been invited to address the Republican Women of Greater North Texas about the critical importance of maintaining free speech for the maintenance our Constitutional Republic. I can now speak from very personal experience.
I would like to conclude by stating that I believe this decision is almost certainly the result of outside pressure being brought to bear on Amazon—the sort of outside pressure from the U.S. Executive Branch that was revealed in discovery in Missouri v. Biden.
At companies like Facebook, Twitter, Google, and Amazon, the upper management levels had always included veterans of the national security establishment. But with the new alliance between U.S. national security and social media, the former spooks and intelligence agency officials grew into a dominant bloc inside those companies; what had been a career ladder by which people stepped up from their government experience to reach private tech-sector jobs turned into an ouroboros that molded the two together.
I strongly suspect that the banning of our book from Amazon has the fingerprints of Biden administration or intelligence agency goons all over it.
For those who would still like to purchase our book, please visit our website by clicking on the image below.
Pandemic restrictions were an unmitigated failure, and the evidence base against the politicians and “experts” who imposed them and demanded compliance continues to grow.
And it raises some substantial questions about holding those responsible accountable for their actions. Especially as mask mandates return in certain parts of the country, with hints of more on the way.
Recently a new government report from the United Kingdom was released to little fanfare, which not-so-surprisingly mirrors the fanfare resulting from the release of new data from the CDC itself, showing how vaccine efficacy has fallen to zero.
Finally, Rochelle Walensky did acknowledge publicly that the vaccines couldn’t stop transmission. However it was already far too late to matter.
But all along the agency has strongly stated that the mRNA shots were effective at preventing hospitalizations. Or at least that the latest booster was effective, tacitly acknowledging that the original 2=dose series has lost whatever impact it once had.
What The Evidence Says About NPI’s
The UK’s Health Security Agency (HSA) recently posted a lengthy examination on the effectiveness of non-pharmaceutical interventions at preventing or slowing the spread of COVID-19 in the country.
And at the risk of revealing a spoiler alert, it’s not good news for the COVID extremists determined to bring mask mandates back.
The goal of the examination was laid out succinctly; the UK’s HSA intended to use primary studies on NPIs within the community to see how successful or unsuccessful they were at reducing COVID infections.
The purpose of this rapid mapping review was to identify and categorise primary studies that reported on the effectiveness of non-pharmaceutical interventions (NPIs) implemented in community settings to reduce the transmission of coronavirus (COVID-19) in the UK.
Streamlined systematic methods were used, including literature searches (using sources such as Medline, Embase, and medRxiv) and use of systematic reviews as sources to identify relevant primary studies.
Unsurprisingly, they found that the evidence base on COVID interventions was exceptionally weak.
In fact, roughly 67 percent of the identified evidence was essentially useless. In fact two-thirds of the evidence identified was modeling.
Two-thirds of the evidence identified was based on modeling studies (100 out of 151 studies).
There was a lack of experimental studies (2 out of 151 studies) and individual-level observational studies (22 out of 151 studies). Apart from test and release strategies for which 2 randomised controlled trials (RCTs) were identified, the body of evidence available on effectiveness of NPIs in the UK provides weak evidence in terms of study design, as it is mainly based on modelling studies, ecological studies, mixed-methods studies and qualitative studies.
This is a key learning point for future pandemic preparedness: there is a need to strengthen evaluation of interventions and build this into the design and implementation of public health interventions and government policies from the start of any future pandemic or other public health emergency.
Modeling, as we know, is functionally useless, given that it’s hopelessly prone to bias, incorrect assumptions and the ideological needs of its creators.
The two paragraphs which followed are equally as important.
Low quality evidence is not something that should be relied upon for decision making purposes, yet that’s exactly what the UK, US and many other countries did. Fauci, the CDC, and others embraced modeling as fact at the beginning of the pandemic. They then repeatedly referenced shoddy, poor quality work because it confirmed their biases throughout its duration, with unsurprising results.
And this government report concurs; stating simply and devastatingly, “there is a lack of strong evidence on the effectiveness of NPIs to reduce COVID-19 transmission, and for many NPIs the scientific consensus shifted over the course of the pandemic.”
Of course the scientific consensus shifted over the course of the pandemic because, as we learned, it became politically expedient for it to shift.
As their paragraphs on the available evidence show, there was little solid, high-quality data showing that NPI’s were having a significant impact on the spread of the virus, a reality that had been predicted by decades of pandemic planning.
But the consensus shifted towards NPIs and away from something approaching Sweden’s strategy or the Great Barrington Declaration, simply because Fauci, the CDC, and other “experts” demanded it shift to suit their ideological aims.
The few high-quality studies on say, masking, that were conducted during the pandemic showed that there was no benefit from mask wearing at an individual or population level. And that is why the Cochrane review came to its now infamous conclusion.
Instead of acknowledging that they were relying on poor quality evidence, the “experts” operated with an unjustified certainty that their interventions were based on following “The Science™.” At every turn, when criticized or questioned, they would default back to an appeal to authority; that the consensus in the scientific community unequivocally believed that the evidence showed that lockdowns, mandates, travel restrictions, and other NPIs were based on the best available information.
After initially determining that the UK should follow Sweden’s example and incorporate a more hands-off approach that relied on protecting the elderly while allowing immunity to build up amongst the younger, healthy populations, Boris Johnson panicked, at the behest of Neil Ferguson, and terrified expert groups. Tossing out decades of planning out of fear, while claiming publicly to be following science.
Instead, a systemic, detailed review of the evidence base relied on by those same experts has now concluded that there never was any high-quality information suggesting that pandemic policies were justifiable. Only wishful thinking from an incompetent, arrogant, malicious “expert” community, and unthinking, unblinking compliance from terrified politicians using restrictions and mandates without care or concern for adverse effects.
While this new report wasn’t specifically designed to determine how effective NPIs were in reducing transmission, it’s clear and obvious conclusions give away that answer too.
If it were easy to prove that COVID policies and mandates had a positive impact on the spread of the virus, there would be dozens of high-quality studies showing a benefit. And those high-quality studies would be covered in this report, with a strong recommendation to reinstate such mandates in future pandemics.
Instead, there’s nothing.
Just exhortations to do better next time, to follow the actual high-quality evidence and not guesswork.
Based on how little accountability there’s been for the “experts” and politicians who lied about “The Science™,” there’s little doubt that when presented with the next opportunity they’ll be sure to handle it in exactly the same way.
Subverting the tightening noose of censorship, the judicial system has risen, this time at least, as a defender of free expression and professional discourse in Washington State. The Court of Appeals has recently extended a lifeline to Dr. Richard Eggleston, a retired ophthalmologist, in his battle against the Washington Medical Commission’s (WMC) accusations of spreading “misinformation” about COVID-19. This pivotal ruling not only resonates as a triumph for Dr. Eggleston but also echoes across the medical community, bolstering the principle that the crucible of critical discourse should not be chilled by punitive actions.
Dr. Eggleston, from Clarkston, Washington, had penned a sequence of critiques last year in the Lewiston Morning Tribune, challenging the prevailing narratives around COVID-19, specifically deliberating on the safety and veracity of the vaccines. His audacity led to an avalanche of disciplinary actions spearheaded by the WMC in August 2022. Accused of unprofessional conduct and “willful misrepresentation of facts,” the retired eye doctor found himself thrust into the cauldron of a legal and professional maelstrom.
As the waves of allegations crashed down, Eggleston invoked his First Amendment right to free speech, refuting the charges with a motion to dismiss. The WMC’s refusal to honor his motion nudged him to escalate the matter to the courts. His quest for justice first encountered a roadblock when the Washington State Superior Court denied his appeal for an injunction. Undeterred, Eggleston propelled his case to the Court of Appeals, which in a moment of judicial prudence, awarded him an emergency injunction in May, halting the impending court proceedings.
The saga witnessed a fresh chapter last week when Court of Appeals Commissioner Hailey L. Landrus sanctioned Eggleston’s motion for a discretionary review of the previous court’s verdict. Attorney Richard Jaffe, representing Eggleston, lauded the decision as “very good news for all who believe that doctors should be able to publicly criticize” what he termed as COVID-19 “propaganda.” This sentiment was echoed by another counsel for Eggleston, Todd Richardson, who expressed both gratitude and relief at the verdict.
The Fluoride Lawsuit has produced video admissions that may have exposed the nearly 80 year practice of adding the toxin to our nation’s water supply as one of the biggest public health scandals in American history. Attorney Michael Connett, Esq., explains how adding fluoride to drinking water became standard practice in the US and shares the studies that link it with severe disease. Then, he shares exclusive video of court depositions of experts you have to see to believe.
“We know next to nothing about the vast majority of compounds in our diet … ‘Our understanding of how diet affects health is limited to 150 key nutritional components,’ says Albert-László Barabási at Harvard Medical School, who coined the term nutritional dark matter.
“‘But these represent only a small fraction of the biochemicals present in our food’ … The idea that food is a rich and complex mix of biochemicals is hardly news.
“Even the well-known macronutrients — proteins, carbohydrates and fats — are hugely diverse. There’s also a vast supporting cast of micronutrients: minerals, vitamins and other biochemicals, many of which are only present in minuscule quantities, but which can still have profound health effects.”
As noted by New Scientist : “With the USDA as your guide, 99.5% of the components in food are a mystery,” and as noted by Barabási, “It would be foolish to dismiss 99.5% of the compounds we eat as unimportant … We will not really understand how we get sick if we don’t solve this puzzle.”
Searching for nutritional ‘dark matter’
Disturbed by the information gap, an international team of researchers started working on a more comprehensive database a decade ago called FooDB, which as of 2020 contained information on some 70,000 nutritional compounds.
Yet even this database still has a long way to go. An estimated 85% of the nutritional components listed remain unquantified, meaning they know a food contains a particular component, but they don’t know how much.
The health implications of most compounds also remain largely unknown.
New Scientist notes:
“This is also true of individual micronutrients. ‘Consider beta-carotene,’ says Barabási. ‘It tends to be positively associated with heart disease, according to epidemiological studies, but studies adding beta-carotene to the diet do not show health benefits. One potential reason is that beta-carotene never comes alone in plants; about 400 molecules are always present with it. So epidemiology may be detecting the health implications of some other molecule.’
“Another probable cause is the effect of the microbiome on dark nutrients, says [FooDB founder David] Wishart. ‘Most dark nutrients are chemically transformed by your gut bacteria.’
“That’s probably why studies on the benefits of different foods give relatively ambiguous results. We don’t properly control for the variation in gut microflora, or our innate metabolism, which means different people get different doses of metabolites from their food.”
Processed foods are an even greater mystery
The reason I started with that background is because we know even less about the constituents of processed foods and synthetic foods that ignorantly claim to be “equivalents” to whole foods, such as “animal-free meats” or “animal-free milk.”
Food processing alone will often alter the composition of bioactive molecules in a food and hence the food’s impact on health, but today, processed foods also contain a wide array of synthetic chemicals that, prior to the modern era, were never part of the human diet.
As such, they pose incredible risks to long-term health and well-being. Processed foods may also have intergenerational effects.
In recent years, the idea that we can simply replace whole foods with synthetic, genetically modified or lab-grown alternatives that are wholly equivalent to the original food has taken root. In reality, that’s simply impossible.
How can scientists create equivalence when they don’t even know what 85% or more of the whole food they’re trying to replicate consists of?
Common sense will tell you they can’t. It might look, smell and even taste similar, but the micronutrient composition will be entirely different, and as a result, the health effects will be incomparable as well.
Animal-free equivalence is a PR fraud
Take cultured meat, for example. It’s said to be equivalent to real animal meat because it’s grown from animal cells. The cells are then grown in a nutrient solution inside a bioreactor until they become a meat-like slab.
Similarly, Bored Cow animal-free milk is a dairy alternative made with whey protein obtained through a fermentation process, plant-based fats (in lieu of milk fats), citrus fiber (for creaminess) and added vitamins and minerals.
Defenders of cultured meat insist that this product is not “fake meat” but “actual meat,” the only difference is that no animal had to be slaughtered to create it.
Cultured meat and other synthetic foods are also said to be more environmentally friendly. But nothing could be further from the truth.
Their impact is far more akin to that of the pharmaceutical industry than the food industry.
Based on this assessment, each kilo of cultured meat produces anywhere from 542 pounds (246 kilos) to 3,325 pounds (1,508 kg) of carbon dioxide emissions, four to 25 times greater than that of conventional beef.
And this information is only provided to refute those who believe the global warming fallacy.
As noted by the authors, investors have poured billions of dollars into the animal cell-based meat sector based on the theory that cultured meat is more environmentally friendly than beef.
However, according to these researchers, that hype is based on flawed analyses of carbon emissions.
A paper published in the April issue of Animal Frontiers also warned that there are several implications of cell-based meat that need to be considered but aren’t, including the fact that cultured products are not nutritionally equivalent to the meats they’re intended to replace.
The claim that no animals are killed in the process is also false. At present, most cultured or cell-based meats are created by growing animal cells in a solution of fetal bovine serum, which is made from the blood of unborn calves.
In short, pregnant cows are slaughtered to drain the unborn fetus of its blood.
Is it safe to eat tumors?
There are also many unanswered questions surrounding safety. For example, to get the cell cultures to grow, some companies are using immortalized cells, which technically speaking are precancerous and/or fully cancerous.
The reason for using immortalized cells is that normally behaving cells cannot divide forever. Most cells will only multiply a few dozen times before they become senescent (old) and die.
This won’t work when your intention is to grow thousands of pounds of tissue from a small number of cells, hence they use immortalized cells that have no off switch for their replication and can divide indefinitely.
Meat substitutes cultured in this way could therefore be thought of as tumors, seeing how the flesh is entirely made up of precancerous or cancerous cells. Is it safe to eat tumors? We don’t know.
Massachusetts Institute of Technology biologist Robert Weinberg, Ph.D., has proposed that humans can’t get cancer from these cells because they’re not human cells and therefore cannot replicate inside your body.
However, there’s no long-term research to back this theory.
Dietary headaches to come
It’s also important to realize that the nutritional composition and safety of synthetic foods will vary depending on the brand.
When you’re dealing with beef, for example, the meat from one cow will be relatively identical to that of any other cow (one major exception being the way they’re raised and fed).
One wild-caught salmon is comparable to any other wild-caught salmon and each russet potato is more or less identical to every other russet potato.
However since each synthetic food brand uses proprietary ingredients and processes, no two will have identical composition or safety, so even if one is eventually proven safe and nutritious, those results cannot be applied to any other brand.
This variance has the potential to create major problems in the future when all sorts of foods have been replaced with synthetic non-equivalents.
How do you determine which cultured beef, chicken or salmon brand might be best for you? How will you devise a sensible diet plan when every food comes in myriad variations of varying composition and safety?
Synthetic foods pose unique food-safety hazards
Many synthetic food proponents claim lab-created food will bypass a host of food-safety problems, but the converse is far more likely to be true.
Sure, beef, for example, can be contaminated during processing, packaging, transport or storage, or during the cooking process.
But in cultured meat, every ingredient and processing step brings with it the potential of contamination and any of the hundreds of ingredients could have toxic effects, alone or in synergy.
Indeed, an in-depth analysis of the available evidence by the Food and Agriculture Organization of the United Nations and a World Health Organization expert panel, published in May, concluded there are at least 53 potential health hazards associated with lab-grown meat.
Among them are the possibility of contamination with heavy metals, microplastics, nanoplastics and chemicals, allergenic additives, toxic components, antibiotics and prions.
What’s more, some of the ingredients that go into synthetic biology like cultured meat are regulated as “non-detectable manufacturing aids,” and you won’t even know what they are. Israeli startup Profuse Technology, for example, has developed a growth media supplement that massively encourages protein growth.
As reported by Food Navigator Europe in an article titled, “Cultivated Meat ‘Breakthrough’: Media Supplement Achieves Full Muscle Maturation on Scaffold Within 48 Hours,” the supplement reduces the time to grow filets and steaks by 80% and augments the protein in the final product by a factor of five.
An unsustainable model
The cultured meat process also produces toxic biowaste — a problem that doesn’t exist in conventional agriculture and food processing. In the video above, Alan Lewis, vice president of government affairs for Natural Grocers, reviews what goes into the making of synthetic biology.
The starting ingredients are typically cheap sugars and fats derived from genetically engineered corn and soy, grown in environmentally destructive monocultures with loads of herbicides, pesticides and synthetic fertilizers.
As a result, they’re loaded with chemical residues. Hundreds of other ingredients may then be added to the ferment to produce the desired end product, such as a certain protein, color, flavor or scent.
The most often used microorganism in the fermentation process is E. coli which has been gene-edited to produce the desired compound through its digestive process.
The microorganism must also be antibiotic-resistant since it needs to survive the antibiotics used to kill off other undesirable organisms in the vat.
As a result, antibiotic-resistant organisms also become integrated into the final product, and the types of foodborne illness that might be caused by gene-edited antibiotic-resistant E. coli and its metabolites are anyone’s guess.
In addition to the desired target metabolite, these gene-edited organisms may also spit out non-target metabolites with unknown environmental consequences and health effects. But that’s not all. Once the target organisms are extracted, what’s left over is hazardous biowaste.
While traditional fermentation processes, such as the making of beer, produce waste products that are edible by animals, compostable and pose no biohazard, the biowaste from these synthetic biology ferments must first be deactivated and then must be securely disposed of. It cannot go into a landfill.
Protect your health by avoiding ‘frankenfoods’
Making food that requires genetically modified organisms inputs and produces more CO2 than conventional farming and hazardous biowaste to boot is hardly a sustainable model.
But then again, synthetic biology and processed foods are not being pushed out of true concern for sustainability.
If that was the goal, everyone would be looking at regenerative agriculture where every part of the system supports and sustains other parts, thereby eliminating the need for chemical inputs, radically reducing water needs while optimizing yields.
No, synthetic biology is pursued because it is a formidable control mechanism. Those who own all the synthetic food production will control the world in a very literal sense. To learn more about this plot for control, see “The Fake ‘Food as Medicine’ Agenda.”
In short, the globalists already own and control most of the carbohydrates grown in the world today. By replacing real animal foods with patented lab-made protein alternatives, they’ll have unprecedented power to control the world’s population.
It’ll also grant them greater control over people’s health. It’s already known that the consumption of ultra-processed food contributes to disease, and the benefactor of ill health is Big Pharma.
The processed food industry has spent many decades driving chronic illness that is then treated with drugs rather than a better diet. Synthetic foods will likely be an even bigger driver or chronic ill health and early death.
The fact is, fake meat and dairy cannot replace the complex mix of nutrients found in grass-fed beef and dairy, and it’s likely that consuming ultra-processed meat and milk alternatives may lead to many of the same health issues that are caused by a processed food diet.
So, if you want to really protect your health and the environment, skip pseudo foods that require patents and stick to those found in nature instead.
Does anyone still remember the days when COVID-19 vaccines were reputed to do what other vaccines do – namely, prevent people from getting infected – and hence we were all taught to speak of exceptional ‘breakthrough infections’ when the unexpected, nonetheless, came to pass?
Well, Germany’s ‘state virologist’ Christian Drosten apparently does not remember them either. Drosten is a member of the German Government’s ‘Corona Expert Council’ and is treated as the absolute authority in Germany for all things COVID-19-related. He also, purely coincidentally, developed the notoriously hyper-sensitive COVID-19 PCR testing protocol, which would go a long way to create the COVID-19 pandemic based on the innumerable ‘asymptomatic cases’ it would go on to detect.
Drosten has given a new interview to the German weekly paper Die Zeit on the solemn occasion of the awarding of this year’s Nobel Prize in Medicine to Drew Weissman and Katalin Kariko, two scientists who contributed to developing the mRNA technology underlying the most widely-used COVID-19 vaccines in the West. Drosten praises the decision to award the prize to the mRNA pioneers – “the technology has proven its significance thanks to the authorisation for COVID-19” – and goes on to note that “I’ve had three doses of the vaccine and been infected twice”.
Three doses and he still got infected twice? Well, why does he agree with the Nobel Committee awarding the prize to Weissman and Kariko then?
Drosten’s remark is apparently supposed to help explain why he will not be getting the new ‘variant-adapted’ COVID-19 jab this autumn or donning a facemask when out and about: since, namely, he already has adequate immunity to fend off the virus – not, it seems, thanks to his previous vaccine doses but due to having caught the bug despite them!
Further on in the interview, Drosten makes this assumption explicit. Thus, asked whether the public has to be concerned about new, more highly transmissible Covid variants, Drosten replies:
Two years ago, higher transmissibility due to new mutations always also meant that more people got seriously ill. Simply because immunity against serious outcomes was not yet complete. By now, the overwhelming majority have built up immune defences by way of infections which are directed against the whole virus, not only against the spike protein from the vaccine. Infections were required for this.
So, Drosten now speaks (and it is not the first time) as if the idea all along was for people to get the vaccine and the virus. He adds, however, that vaccination was still worthwhile, since, he claims, it reduced the severity of the illness when people got infected. Mind you, he has just said that “complete immunity” even against severe disease is only achieved via infection.
The somewhat bewildering position adopted by Drosten is, by the way and not surprisingly – he is not referred to as Germany’s ‘state virologist’ for nothing – also the official German Government position. The official recommendation of the Standing Committee on Vaccination (STIKO) of the German public health authority is that everyone over 18 years of age should have acquired a “basic immunity” by way of at least three “antigen contacts”, either in the form of vaccine doses or infections. The STIKO, however, insists that at least two of these “contacts” should have taken place by way of vaccination, thus suggesting that vaccine-induced immunity is somehow superior to natural immunity, whereas Drosten’s remarks clearly suggest the contrary.
In its latest recommendation on the new ‘variant-adapted’ jab, moreover, the STIKO notes that “the majority of the population has already been vaccinated multiple times and has acquired good basic immunity thanks to having had SARS-CoV-2 infections in addition”. This is why, incidentally, the STIKO only recommends the adapted jab for persons over 60 and members of other ostensibly high-risk groups, but not for anyone else. But the tenor is exactly the same as in Drosten’s remarks, as if getting vaccinated and then getting sick had been the plan all along.
Well, for Drosten’s and the STIKO’s benefit, the below comes directly from the European Medicines Agency summary document on what is by far the most-widely used COVID-19 vaccine in the EU: BioNTech’s mRNA-based ‘Comirnaty’.
Comirnaty was authorised to prevent COVID-19, not to prevent severe outcomes. If it does not prevent COVID-19, it failed.
Robert Kogon is the pen name of a widely-published journalist covering European affairs. Subscribe to his Substack and follow him on X.
Most people are aware of Thalidomide, many are aware of Valproate, but there are several other drugs that have caused birth defects in children that are less well known including Debendox, Carbimazole and Primodos.
Primodos families achieved a main house parliamentary debate on 7th September led by Yasmin Qureshi. Whilst the House was not well attended, every single MP in the Chamber was on the side of the families and little effort was made to defend Government and regulator action.
Yasmin Quereshi explained:
“Children were born with serious deformities due to the hormone pregnancy test drug Primodos, which was taken by expectant mothers between 1953 and 1975”
“The UK regulator first received a warning about the drug in 1958. A definitive study was published in 1967, which linked birth defects to the synthetic hormones in Primodos. Baroness Cumberlege concluded that Primodos should have been removed from the market in 1967. The UK regulator failed in its duty of care to women: Primodos was eventually withdrawn in 1978, 20 years after the first warning.”
Finland, Sweden, Holland and Norway banned the use of hormone pregnancy tests at least 7 years earlier by 1971. MPs passionately recounted many stories of harm caused to their constituents, including Allan Dorans who explained the impact on Nan’s daughter Michelle in 1975, 4-5 years after it was withdrawn in other countries.
Why is the UK always so late to act on medicine harm?
You may say “that was 50 years ago”, things have changed, but MHRA’s lack of action on AstraZeneca covid vaccines resulted in patient deaths as recently as 2021. If anything, the MHRA’s recent transformation from “From watchdog to regulator” (as proclaimed by June Raine) is making things worse. As was pointed out several times during the debate, Primodos was 40 times the strength of the contraceptive pill, this is a risk a lay person can understand, why didn’t the regulator?
Sir Jacob Rees-Mogg stated “The drug was used in South Korea and Germany as an abortifacient. It was used to procure abortions.” Why would MHRA allow a drug that is used overseas for abortions, as a pregnancy test? It would be reasonable to assume there could be a risk of miscarriage. Why did MHRA reject Professor Carl Heneghan’s (director of the Centre for Evidence-Based Medicine at Oxford University) report showing “a clear association” between Primodos and several forms of malformation? Why hasn’t MHRA taken the actions recommended by the Cumberlege report? The yellowcard system is clearly not fit for purpose and is resulting in unnecessary harm to patients.
The Perseus Group believes that a large part of the problem is that medicine safety doesn’t follow the best practice safety management practices of other safety critical sectors like aviation or nuclear. For example, MHRA does not set safety thresholds for the number of deaths/injuries which is allowed before a medicine is suspended. Previous Inquiries, such as the Cumberlege Inquiry, do little or nothing to improve the fundamentals of MHRA’s safety management because there is no input from those involved in managing safety in other safety critical sectors.
The Government committed to take action on Primodos after the Cumberlege report (if fact Primodos was a key driver resulting in the commissioning of the report), but they have limited that action to pelvic mesh and Valproate. The Patient Safety Commissioner role was created to close the gap but again her scope has been limited to mesh and Valproate. Primodos families have been fighting for decades for redress but the system is against them, they have been failed by the Government, the legal system and the regulator.
There are dozens of medicine and medical device victim groups (antidepressants, morning sickness medicines, vaccines etc) fighting their own battles for justice, what is the underlying theme?
A regulator failing to do their duty to keep people safe, influenced by pharmaceutical companies and defended by the Government.
Esther McVey stated “Sadly, Primodos is not an isolated case, and we have seen many examples over the years of our regulatory bodies failing to keep patients safe from new medicines and medical devices. In 2013, the Medicines and Healthcare products Regulatory Agency listed 27 medicines that had been withdrawn on safety grounds. The average time they were on the market was 11 years. I wonder how many times we will allow history to repeat itself. There have been reports and reviews calling for reform, and back in 2004 the Health Committee undertook an inquiry into the influence of the pharmaceutical industry. It noted, of drug companies, the ‘closeness that has developed between regulators and companies’”
Of MRHA’s 16 board members, 6 have Declarations of Interest relating to healthcare companies including pharmaceutical giants such as Sanofi, AstraZeneca and Pfizer. Pharmaceutical companies have been given immunity for several medicines by the Government, incentivizing them to support the pharmaceutical companies position rather than the victims. Pharmaceutical companies already have deep pockets, why are the Government willing to support them rather than those harmed?
Sitting from the outside, I see many victim groups fighting their individual battles in silos. Imagine their power if they all came together as a single voice demanding reform of MHRA? 22 MPs spoke in the Primodos debate, every single one of them wanting justice for the victims. The Parliamentary Under-Secretary of State for Health and Social Care Maria Caulfield has agreed to meet with families and review the findings of the Cumberlege report, so this looks like a small step forwards for this group or at least a little more hope.
Do we now have the critical mass to demand reform of MHRA? If everyone came together, could we get a regulator that prioritises patient safety over pharmaceutical company profits?
Facebook has once more found itself at the helm of controversy regarding the censorship of accurate information concerning COVID-19. This is not the maiden voyage of the social media giant into the tempestuous waters of information control; earlier this year, Meta CEO Mark Zuckerberg conceded to having stifled truthful content about the pandemic at the behest of establishment voices.
His admission followed on the heels of both the US government and the World Health Organization declaring the curtain call on the COVID-19 public health emergency. This prompted Meta to retrench its medical “misinformation” policy, albeit the platform seemingly persists in its endeavor to silence certain narratives.
As reported by Public, the latest instance of censorship came to light when Facebook initiated a fact-check, labeled, and curtailed the visibility of an article titled “Covid Vaccine mRNA In Breast Milk Shows CDC Lied About Safety.” The scrutiny led by Facebook was not aimed at debunking the veracity of the article but instead was targeted at what it deemed as “missing context.”
The article, based on a recent Lancet study, brought to the public’s attention evidence of trace amounts of vaccine mRNA in breast milk, a finding that contradicts previous assurances by the CDC.
Despite the fact that these women were side-stepped in the original vaccine trials, they were given the green light for vaccination, based on the CDC’s now-questionable advice.
Facebook’s audit extrapolated the “context” that pregnant women ought to proceed with vaccination, thereby sidelining the primary discourse of the article which was to shed light on the misleading information dispersed by the CDC.
The methodology employed by Facebook in this instance extends beyond a mere examination of facts. By reducing the spread of the article, the platform effectively stifles a critical examination of the claims made by government health authorities, thereby undermining the public’s right to be informed and to engage in crucial discourse.
Facebook’s ongoing dalliance with censorship, especially of critical health-related information, raises significant questions about the role of social media platforms in the contemporary information ecosystem. The unfurling narrative underscores the necessity for a transparent, decentralized, and accountable framework for information dissemination, one that is immune to undue influence and serves the collective endeavor for truth.
The ongoing war between the US Security State and the First Amendment is perhaps the most underreported development of the 21st century. Now, Missouri v. Biden may bring it to the Supreme Court.
Just two decades ago, the internet promised liberation as dictatorships would cave to the emerging swell of information. That was the hope, at least.
“There’s no question China has been trying to crack down on the internet,” President Clinton said in 2000. “Good luck. That’s sort of like trying to nail Jell-O to the wall.”
That optimism did not come to fruition. Instead of Westernizing the Orient, technology laid the foundation for the US Security State to pursue unprecedented social control.
At first, the conflict appeared to be between rank-and-file military members and transgressive cyber actors. Julian Assange and Edward Snowden seemed like mere hackers, not harbingers for the impending suspension of American liberty.
The battle suddenly became a civilizational struggle in 2020. A highly efficient technocracy declared war against the Bill of Rights. The US Security State shut down American society, eradicated due process, and captured the public health apparatus. The CIA bribed scientists to cover up the origins of Covid, and the Department of Homeland Security dictated what Americans could and could not see in their newsfeeds. The FBI helped banish the country’s oldest newspaper from Twitter for reporting on its preferred candidate’s son.
When Clinton made his “Jell-O” comment, few of us could imagine that we’d live in such a country. We trusted our courts and our elected government to protect us. We thought the rule of law was sacrosanct. We were wrong.
Now, however, the judiciary has the opportunity to reclaim the First Amendment from the tyranny of the Security State in Missouri v. Biden.
Missouri v. Biden and the CISA Injunction
Tuesday, the Fifth Circuit reinstated an injunction against CISA, an agency in the Department of Homeland Security, that prohibits its agents from colluding with social media companies to promote censorship of any kind.
The case demonstrates how far the United States has strayed from its former free speech ethos. CISA held ongoing meetings with social media platforms to “push them to adopt more restrictive policies on censoring election-related speech,” according to the Fifth Circuit. This included criticism of lockdowns, vaccines, and the Hunter Biden laptop. Through a process known as “switchboarding,” CISA officials dictated to Big Tech platforms what content was “true” or “false,” which became Orwellian euphemisms for acceptable and prohibited speech.
CISA’s leaders reveled in their usurpation of the First Amendment. They overturned hundreds of years of free speech protections, appointing themselves the arbiters of truth. Without freedom of “election-related speech,” we no longer live in a democracy. They pursued a faceless dictatorship.
They sought to eradicate dissent surrounding the policies that they imposed. CISA had been responsible for dividing the workforce into categories of “essential” and “nonessential” in March 2020. Hours later, the order became the basis for the country’s first “stay-at-home” order, a process that quickly spiraled into a previously unimaginable assault on Americans’ civil liberties.
CISA betrayed the country’s founding principle. A group of unelected bureaucrats hijacked American society without ever having a vote cast in their names. They disregarded the First Amendment, due process, and elected government in their pursuit of power.
The Framers understood that liberty relied on the free flow of information. They were well aware of the dangers of widespread lies and an incendiary press corps, but tyranny presented a far greater risk to society. Government could not be trusted to wield power over the minds of men, so they enshrined freedom of press, worship, and speech in our Constitution.
The Security State unwound those liberties. White House officials used the power of the federal government to suppress dissent. The Biden Administration launched an interagency attack on free speech. The Covid regime’s coup d’etat continued unimpeded until Judge Terry Doughty’s July 4 injunction.
Now, the Fifth Circuit has remedied its previous error by reinstating the injunction against CISA. The case may now head to the Supreme Court, where the Justices would have the opportunity to dismantle the technocratic censorship operation at the heart of the Covid response.
The war is far from won. Julian Assange remains in jail alongside terrorists for publishing news reports that undermined the Security State’s deceit surrounding the War on Terror. Edward Snowden is banished from his homeland for exposing the lies of James Clapper.
President Biden’s “misinformation” crusade shows no signs of retreat entering the 2024 election cycle. Social media is still censored. Your Google results are still gamed at the behest of powerful state actors. YouTube has proudly announced that it will censor content based on the diktats of the World Health Organization. Say the wrong thing on LinkedIn and you are toast.
Among the large players, only X, formerly known as Twitter, is eschewing routine takedowns of speech deemed oppositional to regime priorities. That is truly only because one man had the means to buy and the drive to liberate it from the Censorship Industrial Complex, for now.
Tuesday’s decision reaffirmed what the Supreme Court called the “bedrock principle underlying the First Amendment” in 1989: “that the government may not prohibit the expression of an idea simply because society finds the idea itself offensive or disagreeable.”
Rebuilding from the wreckage of Covid will require reclaiming those fundamental pillars of American society. The freedom to speak was not the first right earned by a people in revolt against ancient-world forms of statism but it might be the most essential. That’s why it is instantiated in the very first amendment to the Bill of Rights.
If the regime can control the public mind, they can control everything else too. A loss here is a loss everywhere.
Few who consider the recent history of medicine are surprised by the heavy-handed tactics of health regulatory agencies and the attempt by international organizations to dominate the formation of medical policies.
Recent developments are a culmination of practices implemented over many years, that have been and continue to be — strikingly apparent.
The ethos of modern healthcare is exemplified in an anecdote about Dr. Max Gerson when he first came to the United States. Dr. Gerson was a respected physician in Europe, who had great success in treating arthritis, tuberculosis, and cancer with diet. He escaped from Nazi Germany just as his knowledge and techniques were being hailed as effective and revolutionary. Dr. Gerson’s reputation preceded him, and many doctors were seeking his opinion and assistance — until he was confronted by the mentality of the American medical establishment.
Dr. Gerson was called to New York as a consultant for a wealthy industrialist who had arthritis. He had successfully treated the patient’s brother-in-law in Europe. In a Park Avenue penthouse, he joined the house physician and another consulting specialist to see the patient. After the examination, the three physicians retired to discuss the case. Dr. Gerson proceeded to explain the treatment for arthritis he had so successfully used in Europe, then described the manner in which he expected the patient to recover. There was an awkward pause. Finally, one of the other doctors said, “Dr. Gerson, you don’t understand. This man is a wealthy member of the W.R. Grace family. They own steamship lines, banks, chemical companies, and so on. You don’t cure a patient like this, you treat him.”
This simple, insidious message drives most aspects of the medical world. The motivation to keep people healthy is completely undermined by the permeation of profiteering throughout a deeply corrupted industry that depends on the vulnerability of the suffering.
Dr. Gerson’s conclusion that most illness is related to poor diet — and thus correctible, particularly in the early stages of disease — continues to be minimized and ridiculed.
The Confidence Game
There are certainly well-meaning and brilliant physicians; some nobly struggle to practice outside the constraints of conventional wisdom and financial incentives. Most attempt to do the best they can for their patients. But most are thwarted by the theft of their moral compass; their compassion has been hijacked by the greed of corporate interests that have taken healthcare into a destructive realm.
Practitioners and clinics are cornered into using a narrow set of profitable, yet ineffective treatments in changing the course of disease.
Doctors with the best motivation are powerless against the assault from corporate forces. Even if they have the will to cure someone, the structure of the business manipulates them into seeing patients as their source of income. An inextricable relationship with pharmaceutical companies provides an endless supply of products that treat symptoms rather than supporting immunity and good health.
Discussions of the true causes of illness and what is needed to cure them are outlawed. Anyone who strays outside the corporate guidelines is deemed dangerous and a quack — and threatened with losing their license to practice medicine.
Within this restricted environment, all traces of fair compensation have disappeared from healthcare. There is no other service or product that doesn’t provide some estimate of pricing in advance; a model for compensation has no equal. Those with acute or chronic conditions enter the doors of a doctor’s office or hospital without a clear opportunity to ask what they will need to pay. And this happens — with no guarantee that they will be helped — while defenseless against a hurried and fearful dynamic.
The integrity of any healthcare system can be evaluated by whether or not it takes advantage of those who are suffering — andfurtherappraised by the devotion of the necessary time and effort to give lasting support to individual patients.
Suffering Means Profits
People with illness or pain are hostages to the medical establishment. Most who are in physical or mental agony easily give up their autonomy to authorities who apply symptomatic solutions that often suppress illness.
Pharmaceutical interests and government agencies have steadily displayed how their merger has little to do with the well-being of individuals. The muted reaction of the public to this damaging corruption exposes the culmination of a conditioned response that has been developing for decades.
The ability to choose one’s preferred methods of prevention and treatment had been diminishing long before the global efforts to enforce isolation, masking, and vaccination. The doctor-patient relationship has been manipulated and defiled by the same, increasingly powerful economic and political forces.
This ethical depravity of modern medicine has become more apparent in recent years. The increasingly restrictive economic structure that doctors work within is a symptom of this degradation — most obvious during a public health crisis.
Those who dominate the sales of drugs rely on a simple concept: The greater the threat of severe symptoms or death, the narrower the scope of treatment is deemed appropriate and viable, with more potential for profits.
This skewed prioritization has allowed the largest part of gargantuan healthcare profits to be pocketed during the last few weeks of a patient’s life.
Whether for acute, chronic, or infectious diseases, the general public blindly embraces the orders of agencies and doctors who inform them of their vulnerability and the need for medicine. They are simply threatened; drug protocols must be strictly followed, or pandemonium will ensue. Seemingly incontestable facts and decrees overwhelm any personal discretion.
This unprecedented plethora of harmful actions causes incalculable damage to society. A consortium of drug pushers and authoritarian leaders have created an endless war on disease, coercing physicians to peddle their potions — while lifting them from pedestals to the pulpit of supreme medical arrogance.
Poison
Long before the advent of vaccine injuries, an untold number of medical problems were caused by prescribed drugs.These iatrogenic disorders continue to be a leading cause of suffering,hospitalizations, and death.
Within any medicine chest in America, a hideous picture is revealed. The addiction to pharmaceuticals is so entrenched that a good diet, fresh air, balanced living, and restful sleep are minimized and overwhelmed by bogus and suppressive products.
The height of this dehumanizing sales effort has been the description of some narcotics as non-addictive; causing the deaths and destruction of millions of lives.
The flagrant marketing of noxious medications to the ill is only surpassed by the mandating of untested drugs for healthy people. No hawking is necessary; vaccines are hailed as an unassailable defense against sickness and death. Whereas other medications require patients to be diagnosed to sell a product, vaccines can be dispensed to those who have no symptoms, merely using the threat of disease to push inoculation. The government has ensured that while they are experimental, liability is diminished.
That they are described as free is a staggering lie. The inverse is true; inoculations have a special status as a commodity with unrivaled profitability as they can be forced on anyone, particularly when distributed by governments — whose revenues come from taxpayers.
This corruption is relentless. The marketing of vaccines to those who receive no benefit and are likely to suffer subtle or life-changing damage has no limitations. Without the restraint of any truth, the definitions of vaccine and adverse reaction have been changed to maximize proceeds and diminish liability.
This boundless world of profiteering has allowed the vaccination of healthy infants and children; an unmatched, abominable, unforgivable crime.
The illicit behavior of the heavy-handed forces in the medical establishment only becomes more apparent. The recent escalation in threats to streamline and mandate public health policy overtly confirms the blind faith that has been given to an industry that has lost the ability to care for patients and nurture self-healing.
The same foundations, corporations, and organizations that pretend to have humane priorities have consistently promoted poisonous pharmaceuticals and repressed all forms of natural and alternative medical care. This is simply because preventative and remedial methods have minimal cost and lasting effects — and return responsibility for good health to the individual.
The eradication of personal medical autonomy has been a priority of the forces of pharmaceutical interests and corporate medicine for well over a century.The dispensing of poisonous medications is a critical element of this disastrous scheme.
Conclusion: This Is Organized Crime
It is no secret that money is the primary driver of the pharma and medical industries; monopolizing healthcare is the priority of investors. This obvious defect of modern medicine in facing human suffering and disease is rarely discussed. Within the ceaseless debate about overhauling the healthcare bureaucracy, few dare to mention how orientation toward profits has completely corrupted the ethics of medicine.
Almost every challenge and crisis in healthcare has been engendered by the relentless effort to diminish the availability of rival products or treatments. An industrial competitive mindset has been applied to promoting lucrative symptomatic drugs and therapies. The profits from a vast range of prescribed pharmaceuticals that impact symptoms rather than causes — are only exceeded in damaging effects by unnecessary and dangerous inoculations — distributed by the same criminal racket.
As the proceeds of the medical and pharmaceutical industries increase directly with the threat or escalation of disease, complicit authorities show no concern for engendering a healthy world.
Although personal health and general welfare are invoked as reasons to follow medical orders or join the cult of the vaccinated, there is a spurious insistence to accept instructions without question or doubt. This militaristic state of healthcare remains unchecked. Rather than providing safeguards and supporting wellness, ultimatums demanding toxic treatments are sabotaging the vitality of those who fearfully obey coercive dictates.
Reasons for compliance are explicitly described by the enforcers — you need our protection, or else — anyone who doesn’t obey is threatened, degraded, and ridiculed for not surrendering to the edicts of the mafia-like, medical-industrial complex.
The abhorrent means of extortion of an organized crime protection racket are now the standard practices of the pharmaceutical industry and their cronies; government agencies and doctors are their enforcers.This reckless atmosphere allows associated criminal activity, including the engendering of disease through negligent oversight of toxic causes and experimentation with pathogens.
The insidious machinations of a criminal consortium reveal the pernicious influence of money on medical policy and practice. Until this primary failure in providing support for the suffering is recognized and addressed, human health will continue to deteriorate.
A ruling on Tuesday by the US Court of Appeals for the Fifth Circuit marks a leap for the safeguarding of free speech within the social media arena. This decision sees the addition of the Cybersecurity and Infrastructure Security Agency (CISA) to a preliminary injunction in the ongoing legal contest of Missouri v. Biden.
Initially, a host of prominent agencies, including the White House, US Surgeon General’s office, CDC, and the FBI were barred from manipulating social media platforms in a manner that obstructs constitutional freedoms of speech.
The fight against censorship is far from novel, with the tale of Drs. Jayanta Bhattacharya, Martin Kulldorff, and Aaron Kheriaty, and Ms. Jill Hines circulating in the public domain for several years. Their experiences of being censored and throttled on social media platforms form an integral part of a broader governmental agenda to curb free speech for independent thinkers and intellectuals.
This latest ruling by the Fifth Circuit punctuates a series of preceding actions, including its September 8 ruling upholding an earlier order by District Judge Terry Doughty. Doughty’s order on Independence Day caused shockwaves by banning government officials from using their offices to manipulate social media companies into surrendering the First Amendment rights of citizens.
This persistent governmental interference has been described by Judge Doughty as perhaps “the most massive attack against free speech in United States history.” Indeed, it beautifully mirrors a dystopian reality, where a government body, akin to an Orwellian Ministry of Truth, suppresses intellectual discourse and emulation.
The suppression campaign under the Biden administration is far from prejudiced; it has methodically targeted any view conflicting with government narratives. Subjects like natural immunity to Covid-19, vaccine efficacy, origins of the virus, and the effectiveness of mask mandates have become taboo, leading to a wilful silence of experts and common citizens alike.
Such tactics have seen CISA act as a bridge between third parties, flagging potentially problematic content. Having regular interactions with social media platform representatives, they have exploited their authoritative position by pushing them to adopt practices aligned with their censorship agenda.
This has led the Fifth Circuit Court to reassess their previous position. Contrary to their September ruling which stated that communication between CISA and social media companies was constitutional, they now acknowledge that CISA had crossed the line of mere information sharing and actively influenced content moderation policies, leading to the demotion and removal of posts.
While the court order stands, a 10-day stay allows the government to seek permission for a review of the decision by the U.S. Supreme Court.
Peter Gøtzsche reviewed every randomised mammography screening trial ever conducted for the Cochrane Collaboration. Cochrane’s headline is that, assuming a 15% mortality reduction, one woman in 2000 avoids dying of breast cancer over ten years. Ten are overdiagnosed and treated. Two hundred experience false alarms.
But that headline assumes the reduction. When Gøtzsche looked only at the trials with adequate randomisation — the higher-quality ones — the reduction disappeared. No effect on breast cancer mortality. No effect on all-cause mortality.
This is the Cochrane finding, published in the establishment’s own database of systematic reviews.
No woman being asked to consent to a mammogram this week knows it.
That is why the new Unbekoming paperback exists. … continue
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