by Nick Corbishley via: Naked Capitalism

So why are journalists not covering it?

Michael Capuzzo, a New York Times best-selling author , has just published an article titled “The Drug That Cracked Covid”. The 15-page article chronicles the gargantuan struggle being waged by frontline doctors on all continents to get ivermectin approved as a Covid-19 treatment, as well as the tireless efforts by reporters, media outlets and social media companies to thwart them.

Because of ivermectin, Capuzzo says, there are “hundreds of thousands, actually millions, of people around the world, from Uttar Pradesh in India to Peru to Brazil, who are living and not dying.” Yet media outlets have done all they can to “debunk” the notion that ivermectin may serve as an effective, easily accessible and affordable treatment for Covid-19. They have parroted the arguments laid out by health regulators around the world that there just isn’t enough evidence to justify its use.

For his part, Capuzzo, as a reporter, “saw with [his] own eyes the other side [of the story]” that has gone unreported, of the many patients in the US whose lives have been saved by ivermectin and of five of the doctors that have led the battle to save lives around the world, Paul Marik, Umberto Meduri, José Iglesias, Pierre Kory and Joe Varon. These are all highly decorated doctors. Through their leadership of the Front Line COVID-19 Critical Care (FLCCC) Alliance, they have already enhanced our treatment of Covid-19 by discovering and promoting the use of Corticoid steroids against the virus. But their calls for ivermectin to also be used have met with a wall of resistance from healthcare regulators and a wall of silence from media outlets.

“I really wish the world could see both sides,” Capuzzo laments. But unfortunately most reporters are not interested in telling the other side of the story. Even if they were, their publishers would probably refuse to publish it.

That may explain why Capuzzo, a six-time Pulitzer-nominated journalist best known for his New York Times-bestselling nonfiction books Close to Shore and Murder Room, ended up publishing his article on ivermectin in Mountain Home, a monthly local magazine for the of the Pennsylvania mountains and New York Finger Lakes region, of which Capuzzo’s wife is the editor. It’s also the reason why I decided to dedicate today’s post to Capuzzo’s article. Put simply, as many people as possible –particularly journalists — need to read his story.

As Capuzzo himself says, “I don’t know of a bigger story in the world.”

Total News Blackout

On December 8 2020, FLCCC member Dr Pierre Kory gave nine minutes of impassioned testimony to the US Homeland Security Committee Meeting on the potent anti-viral, anti-inflammatory benefits of ivermectin. A total of 9 million people (myself included) saw the video on YouTube before it was taken down by YouTube’s owner, Google. As Capuzzo exhaustively lays out, both traditional and social media have gone to extraordinary lengths to keep people in the dark about ivermectin. So effective has this been that even in some of the countries that have benefited most from its use (such as Mexico and Argentina) many people are completely unaware of its existence. And this is no surprise given how little information is actually seeping out into the public arena.

A news blackout by the world’s leading media came down on Ivermectin like an iron curtain. Reporters who trumpeted the COVID-19 terror in India and Brazil didn’t report that Ivermectin was crushing the P-1 variant in the Brazilian rain forest and killing COVID-19 and all variants in India. That Ivermectin was saving tens of thousands of lives in South America wasn’t news, but mocking the continent’s peasants for taking horse paste was. Journalists denied the world knowledge of the most effective life-saving therapies in the pandemic, Kory said, especially among the elderly, people of color, and the poor, while wringing their hands at the tragedy of their disparate rates of death.

Three days after Kory’s testimony, an Associated Press “fact-check reporter” interviewed Kory “for twenty minutes in which I recounted all of the existing trials evidence (over fifteen randomized and multiple observational trials) all showing dramatic benefits of Ivermectin,” he said. Then she wrote: “AP’S ASSESSMENT: False. There’s no evidence Ivermectin has been proven a safe or effective treatment against COVID-19.” Like many critics, she didn’t explore the Ivermectin data or evidence in any detail, but merely dismissed its “insufficient evidence,” quoting instead the lack of a recommendation by the NIH or WHO. To describe the real evidence in any detail would put the AP and public health agencies in the difficult position of explaining how the lives of thousands of poor people in developing countries don’t count in these matters.

Not just in media but in social media, Ivermectin has inspired a strange new form of Western and pharmaceutical imperialism. On January 12, 2021, the Brazilian Ministry of Health tweeted to its 1.2 million followers not to wait with COVID-19 until it’s too late but “go to a Health Unit and request early treatment,” only to have Twitter take down the official public health pronouncement of the sovereign fifth largest nation in the world for “spreading misleading and potentially harmful information.” (Early treatment is code for Ivermectin.) On January 31, the Slovak Ministry of Health announced its decision on Facebook to allow use of Ivermectin, causing Facebook to take down that post and removed the entire page it was on, the Ivermectin for MDs Team, with 10,200 members from more than 100 countries.

In Argentina, Professor and doctor Hector Carvallo, whose prophylactic studies are renowned by other researchers, says all his scientific documentation for Ivermectin is quickly scrubbed from the Internet. “I am afraid,” he wrote to Marik and his colleagues, “we have affected the most sensitive organ on humans: the wallet…” As Kory’s testimony was climbing toward nine million views, YouTube, owned by Google, erased his official Senate testimony, saying it endangered the community. Kory’s biggest voice was silenced.

“The Most Powerful Entity on Earth”

Malcom X once called the media “the most powerful entity on the earth.” They have, he said, “the power to make the innocent guilty and to make the guilty innocent, and that’s power. Because they control the minds of masses”. Today, that power is now infused with the power of the world’s biggest tech and social media companies. Together social and traditional media have the power to make a medicine that has saved possibly millions of lives during the current pandemic disappear from the conversation. When it is covered, it’s almost always in a negative light. Some media organizations, including the NY Times, have even prefaced mention of the word “ivermectin” — a medicine that has done so much good over its 40-year lifespan that its creators were awarded the Nobel Prize for Medicine in 2015 — with the word “controversial.”

Undeterred, many front-line doctors have tried to persuade their respective health regulators of the unparalleled efficacy and safety of ivermectin as a covid treatment. They include Dr. Tess Lawrie, a prominent independent medical researcher who, as Capuzzo reports, evaluates the safety and efficacy of drugs for the WHO and the National Health Service to set international clinical practice guidelines:

“[She] read all twenty-seven of the Ivermectin studies Kory cited. The resulting evidence is consistent and unequivocal,” she announced, and sent a rapid meta-analysis, an epidemiolocal statistical multi-study review considered the highest form of medical evidence, to the director of the NHS, members of parliament, and a video to Prime Minister Boris Johnson with “the good news… that we now have solid evidence of an effective treatment for COVID-19…” and Ivermectin should immediately “be adopted globally and systematically for the prevention and treatment of COVID-19.”

Ignored by British leaders and media, Lawrie convened the day-long streaming BIRD conference—British Ivermectin Recommendation Development—with more than sixty researchers and doctors from the U.S., Canada, Mexico, England, Ireland, Belgium, Argentina, South Africa, Botswana, Nigeria, Australia, and Japan. They evaluated the drug using the full “evidence-to-decision framework” that is “the gold standard tool for developing clinical practice guidelines” used by the WHO, and reached the conclusion that Ivermectin should blanket the world.

“Most of all you can trust me because I am also a medical doctor, first and foremost,” Lawrie told the prime minster, “with a moral duty to help people, to do no harm, and to save lives. Please may we start saving lives now.” She heard nothing back.

Ivermectin’s benefits were also corroborated by Dr. Andrew Hill, a renowned University of Liverpool pharmacologist and independent medical researcher, and the senior World Health Organization/UNITAID investigator of potential treatments for COVID-19. Hill’s team of twenty-three researchers in twenty-three countries had reported that, after nine months of looking for a COVID-19 treatment and finding nothing but failures like Remdesivir— “we kissed a lot of frogs”— Ivermectin was the only thing that worked against COVID-19, and its safety and efficacy were astonishing—“blindingly positive,” Hill said, and “transformative.” Ivermectin, the WHO researcher concluded, reduced COVID-19 mortality by 81 percent.

Why All the Foot Dragging?

Yet most health regulators and governments continue to drag their feet. More evidence is needed, they say. All the while, doctors in most countries around the world have no early outpatient medicines to draw upon in their struggle against the worst pandemic in century. Drawing on his own experience, Capuzzo describes the absence of treatments for COVID-19 as a global crisis:

When my daughter Grace, a vice president at a New York advertising agency, came
down with COVID-19 recently, she was quarantined in a “COVID hotel” in Times Square with homeless people and quarantining travelers. The locks on her room door were removed. Nurses prowled the halls to keep her in her room and wake her up every night to check her
vitals—not to treat her, because there is no approved treatment for COVID-19; only, if her oxygen plummeted, to move her to the hospital, where there is only a single eective approved treatment for COVID-19, steroids that may keep the lungs from failing.

There are three possible explanations for health regulators’ refusal to allow the use of a highly promising, well-tolerated off-label medicine such as ivermectin:

• As a generic, ivermectin is cheap and widely available, which means there would be a lot less money to be made by Big Pharma if it became the go-to early-stage treatment against covid.
• Other pharmaceutical companies are developing their own novel treatments for Covid-19 which would have to compete directly with ivermectin. They include ivermectin’s original manufacturer, Merck, which has an antiviral compound, molnupiravir, in Phase 3 clinical trials for COVID-19. That might explain the company’s recent statement claiming that there is “no scientific basis whatsoever for a potential therapeutic effect of ivermectin against COVID-19.
• If approved as a covid-19 treatment, ivermectin could even threaten the emergency use authorisation granted to covid-19 vaccines. One of the basic conditions for the emergency use authorisation granted to the vaccines currently being used against covid is that there are no alternative treatments available for the disease. As such, if ivermectin or some other promising medicine such as fluvoxamine were approved as an effective early treatment for Covid-19, the vaccines could be stripped of authorisation.

[As a lockdown fanatic and virus hysteria booster the Naked Capitalism leaves out another possibility: An effective treatment would threaten the lockdown complex.]

This may explain why affordable, readily available and minimally toxic drugs are not repurposed for use against Covid despite the growing mountains of evidence supporting their efficacy.

Ivermectin has already been approved as a covid-19 treatment in more than 20 countries. They include Mexico where the mayor of Mexico City, Claudia Scheinbaum, recently said that the medicine had reduced hospitalisations by as much as 76%. As of last week, 135,000 of the city’s residents had been treated with the medicine. The government of India — the world’s second most populous country and one of the world’s biggest manufacturers of medicines — has also recommended the use of ivermectin as an early outpatient treatment against covid-19, in direct contravention of WHO’s own advice.

Dr Vikas P. Sukhatme, the dean of Emory School of Medicine, recently wrote in a column for the Times of India that deploying drugs such as ivermectin and fluvoxamine in India is likely to “rapidly reduce the number of COVID-19 patients, reduce the number requiring hospitalization, supplemental oxygen and intensive care and improve outcomes in hospitalized patients.”

Four weeks after the government included ivermectin and budesonide among its early treatment guidelines, the country has recorded its lowest case count in 40 days.

In many of India’s regions the case numbers are plunging in almost vertical fashion. In the capital Delhi, as in Mexico City, hospitalisations have plummeted. In the space of 10 days ICU occupancy fell from 99% to 70%. Deaths are also falling. The test positivity ratio slumped from 35% to 5% in just one month.

One of the outliers of this trend is the state of Tamil Nadu, where cases are still rising steeply. This may have something to do with the fact that the state’s newly elected governor, MK Stalin, decided to exclude ivermectin from the region’s treatment protocol in favor of Remdesivir. The result? Soaring cases. Late last week, Stalin reversed course once again and readopted ivermectin.

For the moment deaths in India remain extremely high. And there are concerns that the numbers are being under-reported. Yet they may also begin to fall in the coming days. In all of the countries that have used ivermectin widely, fatalities are the last thing to fall, after case numbers and hospitalizations. Of course, there’s no way of definitively proving that these rapid falloffs are due to the use of ivermectin. Correlation, even as consistent as this, is not causation. Other factors such as strict lockdowns and travel restrictions no doubt also play a part.

But a clear pattern across nations and territories has formed that strongly supports ivermectin’s purported efficacy. And that efficacy has been amply demonstrated in three meta-analyses.

India’s decision to adopt ivermectin, including as a prophylaxis in some states, is already a potential game-changer. As I wrote three weeks ago, if case numbers, hospitalizations and fatalities fall in India as precipitously as they have in other countries that have adopted ivermectin, it could even become a watershed moment. But for that to happen, the news must reach enough eyes and ears. And for that to happen, reporters must, as Capuzzo says, begin to do their job and report both sides of this vital story.

by Sarah Knapton via : The Telegraph

Editor’s note: The virus clearly merely brought deaths that would have occurred soon anyway forward (and did so despite all the idiotic, useless, superstitious lockdowns of the healthy and the not-at-risk). You had some excess deaths so now you have missing deaths of the very frail who would be dying now, but instead died during the winter wave. That’s sad but it’s not the Bubonic Plague nor even the Spanish Flu, and in any case lockdowns and face masks didn’t help them but instead caused additional misery, loss of dignity, and death.

______

The proportion of people dying in England fell in April to its lowest level since records began, figures from the Office for National Statistics show.

Just 851.2 people per 100,000 died last month – the lowest figure since the ONS started recording mortality rates in 2001. At the height of the first wave of the Covid pandemic last April, death rates were 1,859 per 100,000.

The latest figures show that 38,899 people died in April – 6.1 per cent fewer than the five-year average [which is 41,426 or 2,527 higher].

Just 2.4 per cent of all deaths mentioned Covid on the death certificate, a 77.6 per cent decrease from March and the largest month-on-month decline since the pandemic began.

The new data provide more evidence that the NHS is in little danger of being overwhelmed in the near future, with deaths from most causes lower than normal. Covid is now the ninth most common cause of death in England and Wales, behind conditions including heart disease, dementia, several cancers and influenza.

Latest figures from King’s College London’s symptom tracker app also suggest that Covid case rates are flat, despite the Indian variant making up an increased percentage of cases.

Last week, the ZOE Covid Study team estimated that there were 2,750 new infections per day in the UK, compared with 2,782 the previous week.

Experts believe the risk of a Covid infection is currently one in 17,205, falling to one in 31,184 after a first vaccine and one in 41,579 after a second.

Although there are localised hotspots in which the Indian variant is spreading, it is not leading to rising case numbers overall, according to King’s data, which tends to be a more up-to-date measure of the state of the pandemic than other figures.

Tim Spector, professor of genetic epidemiology at King’s College, said the team was monitoring the variant closely, but there was nothing to suggest that the NHS was in danger of being overrun or that the lockdown release would need to be postponed.

“So far, we see only localised outbreaks or hotspots,” he said. “Not only in Bedford and Bolton, which we saw a week ago, but our data shows Newport in Wales, Glasgow and neighbouring areas like East Dunbartonshire or Lanarkshire in Scotland, Aberdeen, Leeds and neighbouring authorities like Kirklees and Wakefield too.

“We noticed the same trend previously with outbreaks of the South African and Brazilian variants, but these remained local and didn’t translate into wider cases countrywide. We also saw similar rates last summer in the Midlands, which never produced widespread outbreaks. I expect to see rates stay at similar levels for a while.

“There’s no clear evidence yet that the new Indian variant is significantly worse than the old Kent one. While the outbreaks remain localised and UK numbers are steady and most cases appear mild, it’s highly unlikely to cause the NHS to be overrun or stop us coming out of lockdown.

“So no need to panic, but do stay vigilant and keep logging with the ZOE Covid Study app to stay ahead of the curve and help us monitor outbreaks like these.

PETROPAVLOVSK-KAMCHATSKIY (Sputnik) – Russia’s Chumakov research centre plans to produce at least 7.5 million doses of its coronavirus vaccine CoviVac by the end of the year, the institute’s director general, Aidar Ishmukhametov, said on Sunday.

“By the end of the year, I suppose there will be about 7.5 million [doses] at least”, Ishmukhametov said to the Rossiya 1 broadcaster.

The head of the centre added they had applied for authorisation from the Russian Health Ministry to administer their vaccine to people over 60 years old, noting that immunity developed after the CoviVac shot would last some eight months.

Russia’s Chumakov research centre officially launched production of the nation’s third coronavirus vaccine, CoviVac, in late March.

CoviVac is a so-called whole-virion vaccine based on a modified SARS-CoV-2 virus that is unable to cause the disease but boosts immunity against coronavirus. The vaccine was developed from samples taken from a COVID-19 patient.

via: The Daily Expose

A GP in the United Kingdom has lambasted the relentless and coercive push of the authorities Covid-19 experimental vaccine roll-out and insisted it makes a mockery of informed consent.

Dr Teck Khong, who served as a GP at Pasley Road Health Centre in Leicester for 37 years until March 2019, implied that the general public were not being told the facts about the new Covid vaccines as he suggested they may believe the different brands of vaccines are all the same as each other. Pointing out that even his own GP was none the wiser.

“When I was offered Covid vaccination by my GP, I asked him which it was he was offering me. He thought they were all the same until I explained that there are 7 technological approaches being employed in the making of the 214 vaccine candidates that were in the pipeline or had reached emergency authorisation in December 2020. This impression of homogeneity has been allowed to be glibly glossed over in the mass immunisation programme.” Dr Teck Khong said.

The fact that medical professionals do not know what these “vaccines” actually are or how they work is extremely concerning.

The Pfizer / BioNTech “vaccine” which was approved for emergency use back in December 2020 is an mRNA gene therapy. As is the Moderna jab which is supposed to hit UK shores soon. The mRNA gene therapy has never before been authorised for use in humans, and for good reason.

In the development of vaccines against coronaviruses like SARS-COV-1 and MERS in the early 2000’s, researchers found evidence of a serious problem. Teams of U.S. and foreign scientists vaccinated animals with the four most promising vaccines. At first, the experiment seemed successful as all the animals developed a robust antibody response to coronavirus. However, when the scientists exposed the vaccinated animals to the wild virus, the results were horrifying. Vaccinated animals suffered hyper-immune responses including inflammation throughout their bodies, especially in their lungs.

Many people are under the impression the Oxford / AstraZeneca jab is no different to the traditional vaccines such as the ones used to inoculate against influenza. They couldn’t be more wrong. The AstraZeneca “vaccine” is also a new technology never before authorised for use in human beings. It is a ‘viral vector’ vaccine which uses a chimpanzee common cold viral vector known as ChAdOx1, which injects “code” into the recipients DNA and allegedly instructs it to make the SARS-CoV-2 spike protein.

Dr Teck Khong then went on to lambaste the disingenuous impression that there are no long term consequences of having one of the experimental Covid jabs.

“It is disingenuous to give the public the impression that there are no potential long term sequelae, no more than is the dearth of information that makes the ethical requirement of informed consent a mockery given the relentless and coercive push of the mass immunisation programme.

“We in the medical profession should remain not only vigilant to adverse events in the aftermath of vaccination but must also be advocates of our patients in timely intervention with the most appropriate medicines for any given clinical stage of illness presentation.”

Dr Khong then called for health professionals to support one another to better understand the risks associated with the experimental Covid vaccines, insisting many people may not require vaccination and may be susceptible to developing serious adverse reactions to the jabs.

“Additionally, we must continue to support one another in the understanding of the pathophysiology of causally related adverse events so we are enabled to define with greater accuracy the risk factors of the vulnerable. Indeed, it would appear that many may not require vaccination while some are peculiarly susceptible not only to SARS-CoV-2 but to developing serious reactions to certain classes of the Covid vaccines.”

By Henry Makow Ph.D.

(Victor Rothschild, 1910-1980, the famous “Fifth Man” of the Cambridge Five Spy Ring, gave all the West’s secrets to the USSR.)

In 1942, Sir Mark Oliphant, a leading British physicist was shocked when a messenger delivered a part from his new radar technology with a warning from MI-5 Security Inspector Victor Rothschild to “tighten up your security.”

A few days earlier Rothschild had visited Oliphant’s Birmingham University lab, quizzed him on his research, and pocketed the three-inch diameter magnetron.

But talk about chutzpah!

Baron Rothschild was himself a Soviet agent! Before returning the magnetron, he had transmitted detailed drawings to Moscow, a fact later confirmed by his KGB handlers.

Oliphant related this story in 1994 to Roland Perry, the Australian author of The Fifth Man (1994, Sedgwick and Jackson, 475 pp).

Between 1935 and 1963, the Soviet Union knew all of Britain’s military and scientific secrets thanks to “The Cambridge Five” a spy ring that operated in M1-5, MI-6 and the Foreign Office. Western intelligence agencies were rendered ineffective and Allied secrets, including the design of the atomic bomb, were stolen.

The traitors were Kim Philby, Donald Maclean, Guy Burgess and Anthony Blunt. But there is a natural reluctance to admit that “the Fifth Man” was Nathaniel Meyer Victor Rothschild (1910-1990), the Third Baron Rothschild, the British head of the world’s richest banking dynasty, which controls the Bank of England.

In 1993, after the dissolution of the Soviet Union, six retired KGB Colonels in Moscow confirmed Rothschild’s identity to Roland Perry. Col. Yuri Modin, the spy ring’s handler, went on the record.

Perry writes: “According to …Modin, Rothschild was the key to most of the Cambridge ring’s penetration of British intelligence. ‘He had the contacts,’ Modin noted. ‘He was able to introduce Burgess, Blunt and others to important figures in Intelligence such as Stewart Menzies, Dick White and Robert Vansittart in the Foreign Office…who controlled Mi-6.” (p.89)

You can understand the reluctance. The Rothschilds are undoubtedly the largest shareholders in the world’s central banking system. Victor Rothschild’s career as Soviet agent confirms that these London-based bankers plan to translate their monopoly on credit into a monopoly on everything using government as their instrument, ultimately a “world government” dictatorship akin to Communism.

It adds credence to the claim theRothschilds were behind the Bolshevik Revolution, and used the Cold War and more recently the 9-11 hoax, the bogus “War on Terror” and the Covid Hoax, to advance their world hegemony.

Which is more plausible? One of the richest men in the world, Victor Rothschild espoused Communist ideals so that his own fabulous wealth and position could be taken away?

Or that Communism in fact was a deception designed to take away our wealth and freedom in the name of “equality” and “brotherhood”?

(Evil and Rich)

MAN OF ACTION

According to “The Fifth Man”, Victor Rothschild had an IQ of 184. He was a gifted jazz pianist with an intuitive understanding of many scientific disciplines. He saw banking as a dreary affair and preferred the exciting example of his great grandfather Lionel Rothschild (1808-1879) who Benjamin Disraeli immortalized as “Sidonia” in the novelConingsby (1844).

“No minister of state had such communication with secret agents and political spies as Sidonia. He held relations with all the clever outcasts of the world. The catalog of his acquaintances in the shape of Greeks, Armenians, Moors, secret Jews, Tartars, Gypsies, wandering Poles and Carbonari, would throw a curious light on those subterranean agencies of which the world in general knows so little, but which exercise so great an influence on public events. The secret history of the world was his pastime. His great pleasure was to contrast the hidden motive, with the public pretext, of transactions.” (Coningsby pp. 218-219)

Rothschild studied Zoology at Cambridge where Anthony Blunt recruited him for the KGB about 1936. (Blunt later said it was Rothschild who recruited him, which makes more sense.) Rothschild later joined MI-5 and was in charge of counter sabotage. He instructed the military on how to recognize and defuse bombs. Rothschild was a personal friend of Winston Churchill. Perry writes:

“The two socialized often during the war years. Rothschild used his wealth and position to invite the prime minister to private parties. His entree to the wartime leader, plus access to all the key intelligence information, every major weapons development and his command of counter-sabotage operations in Britain, made Rothschild a secretly powerful figure during the war years…The result was that Stalin knew as much as Churchill about vital information, often before the British High Command was informed.” (xxviii-xxix)

(left, only a society with a death wish would idealize traitors and dupes.)

Rothschild helped neutralize enemies of the Soviet Union who came to the British for support. For example, he was involved in the cover-up of the assassination of Polish war leader and British ally Wladyslaw Sikorski, whose plane was blown up in July 1944. Sikorski had become burdensome to Stalin after he discovered the KGB had massacred 16,000 Polish officers in the Katyn Woods and elsewhere in 1940.

In 1944, Blunt, Burgess and Philby all stayed with Victor at the Rothschild mansion in Paris. Rothschild was briefly in charge of Allied intelligence in Paris and interrogated many prisoners.

After the war Rothschild spent time in the US overseeing attempts to learn the atom bomb secrets. Due in part to the Cambridge Five, Perry says “the Russians knew about every major intelligence operation run against them in the years 1945 to 1963.” (xxxi)

CONCLUSION

Victor Rothschild held many jobs that served to disguise his true role which I suspect was that of a member of the Illuminati Grand Council. (The Illuminati represent the highest rank of Freemasonry.) He was not a lowly agent. He probably gave orders to people like Winston Churchill, FDR and Stalin.

For example, he ensured that the USSR supported the establishment of the State of Israel. “He knew the proper back-channels to reach decision-makers in Moscow,” a KGB Colonel told Perry. “Let us just say, he got things done. You only did that if you reached the top. He was very persuasive.” (176)

T Stokes wrote: ” In the Russian Intel archives Lord and Lady Rothschild are codenamed; “David and Rosa.” Rothschild and Churchill were inseparable during W.W.II. The bankers bought Churchill’s services in W.W.II for a recorded £50,000 to lobby for total war with Germany, and Churchill had a bank account in the name of ‘Colonel Arden,’ to accept these secret donations.”

(Rothschild making a Satanist hand sign)

The fact that Rothschild was protected until his death suggests this is a ruling class conspiracy. According to Greg Hallett, Anthony Blunt, a fellow spy, was an illegitimate son of George V, half-brother and look-alike to Edward VIII, the Duke of Windsor. Until his exposure in 1964, Blunt was knighted and was Curator of the Queen’s art collection. He received immunity from prosecution in exchange for his confession.

Many believe this conspiracy is “Jewish.” Yes, but “generational Satanist” would be more accurate. These Sabbatean Jews intermarry with Gentiles. The current Lord Jacob Rothschild, the Fourth Baron Rothschild is Victor’s son by his first wife Barbara Hutchinson, pictured above, a non-Jew who converted. In Jewish law, Jacob Rothschild is not a Jew. He married Serena Dunn. By the way, Meyer Amschel, Victor’s only son by his second marriage, also to a non-Jew, ‘committed suicide’ in 1996.

While Victor Rothschild pretended to “socialist ideals,” this was just a ruse to entrap misguided idealists. The banker was a conscious traitor. Treason is the template for contemporary politics. The central banking cartel is erecting its “world governance” dictatorship and anyone who wants to succeed must be loyal to the sick new paradigm and a traitor to the genuine old.

While distracting us with sex and sports, our political and cultural “leaders” attack our national, religious, racial and family foundations using war, homosexuality, pornography, feminism, migration and “diversity.”

Clearly, we need new leaders who will stand up to the owners of the world monetary system. The destiny of humanity is at stake.

How can I be expected to obey the law when it takes an “expert” to interpret it?

by Helen Buyniski

US corona czar Dr. Anthony Fauci has been awarded the Dan David Prize for “defending science in the face of uninformed opposition,” joining a rogues gallery of former winners including Jimmy Wales and Tony Blair.

The Dan David Foundation, which is based out of Tel Aviv University and counts such dubious luminaries as war criminal Henry Kissinger on its board of directors, has gifted $1 million to Fauci for “courageously defending science in the face of uninformed opposition during the challenging Covid crisis.”

It’s not clear from whence this “uninformed opposition” emerged – indeed, one of Fauci’s most vocal opponents has been Dr. Anthony Fauci, who spoke up against the wearing of face masks and other mandates just weeks before he came out swinging in support of such rules.

ALSO ON RT.COMTime magazine celebrates medical authoritarianism, naming Fauci ‘guardian of the year’

Presumably, though, the Dan David Foundation was referring to popular opposition to that version of science that more closely resembles religious dogma. Fauci’s smug, self-satisfied and above all brittle variant of “science” cannot be questioned, lest it shatter into a million pieces, and the man’s stubborn use of thought-terminating clichés makes him resemble more of a cult leader than a public health official.

The Dan David Foundation has quite a history of honoring dodgy figures, and it’s no surprise to find them promoting dogmatic Fauci-flavored science over the true scientific method. Wikipedia co-founder and famed fabulist Jimmy Wales was among its prize-winners in 2015, gifted the $1 million treasure for his work in the field of “the Information Revolution.”

While Wales generally defends his truth-averse creation by waxing poetic about a world “in which every person is given free access to the sum of all human knowledge,” Wikipedia has instead mounted a full frontal assault on human knowledge, seeking to destroy all that which does not conform to its founder’s preferred version of reality. Despite presenting itself as an encyclopedia, Wikipedia even admits it does not traffic in “truth,” but merely “verifiability,” and the site’s disclaimer notes “that nothing found here has necessarily been reviewed by people with the expertise required to provide you with complete, accurate or reliable information.”

Fauci is in good company at the Dan David Foundation. Just as the good doctor has done for Big Pharma fraudsters like Pfizer and GlaxoSmithKline, Wales has taken great care to treat Israel and the many “alternative facts” with which it shrouds its own crimes with kid gloves, ensuring the average Wikipedia user doesn’t learn the truth about the horrific oppression Tel Aviv deals out to occupied Palestine on a daily basis.

Guardian writer insists cancel culture doesn’t exist, gets whacked by the granddaddy of all special interests: Big Israel

The Israeli government and its private-sector collaborators have long operated ideologically-driven editing cells, a massive violation of Wikipedia’s rules but one whose owners straight-facedly describe as merely an effort to make Wikipedia “balanced and Zionist in nature.” Many of the Israelis who operate these editing initiatives receive valuable rewards from their government, and some even rise to plum positions therein – Ayelet Shaked became the Israeli Minister of Justice after putting together the pro-(illegal)-settlement Yesha Council’s editing initiative, and Naftali Bennett rose to Education Minister not long after serving in that same organization.

As a Dan David Foundation winner, Fauci will also be mingling with Ezekiel Emanuel, the oncologist who infamously devised the notion of rationing healthcare – “death panels” – and suggested humans should aspire to live to no more than 75 years of age. He won the prize in 2018 for his work as “pioneer in the field of end-of-life care.” You can’t make this stuff up.

Speaking of “end-of-life care,” the Foundation also counted Tony Blair, the former UK PM who joined US President George W. Bush in his illegal and monstrous assault on Iraq, among its winners in 2009. Blair’s bio deems him “one of the most outstanding statesmen of our era,” presumably with a straight face. In his post-PM career, Blair has traveled around giving expensive speeches to repressive dictators and counseling them on how best to extract themselves from pesky human rights charges (see: Kazakhstan, Azerbaijan, UAE and Israel itself), while Wales follows him around like a lovesick puppy, setting up Wikipedia projects for aforementioned dictators. After all, nothing says “democratic” like a “people’s encyclopedia” run like a Ministry of Truth!

And what gathering of ruling class ghouls would be complete without the World Economic Forum’s Klaus Schwab? The real-life Bond villain won the Dan David Prize in 2004 for “his significant contribution in fostering international dialogue and activism to resolve some of the world’s greatest issues.” So what if the corporations that comprise his little organization caused a whole bunch more “issues” in the mean time? Can’t make an omelette without breaking a few eggs!

As a central figure in the US medical establishment for four decades who’s personally presided over the declining life expectancy of its people, Fauci fits perfectly into the malevolent ruling class soup cooked up by the Dan David Foundation. Wikipedia made a formal alliance with the World Health Organization last year, supposedly part of an effort to fight “disinformation” related to the novel coronavirus epidemic, and Wales has long considered his website a prize weapon in the armory of modern medicine against what he calls “lunatic charlatans” – those medical practitioners who dare to dream that cures may exist outside the money-paved halls of Big Pharma.

And Fauci himself is a true believer in the wide world of orthodox pharmaceutical treatments, unwilling to concede any validity on the part of natural medicine and determined to come out of the Covid-19 pandemic looking good – no matter how many people have to die for his public relations campaign.

In reality, Fauci has done a substandard job throughout his tenure, whether it was denying access to a potentially lifesaving antibacterial drug that could have saved the lives of AIDS patients infected with a killer variant of pneumonia or pushing a dangerous swine flu vaccine for an epidemic that turned out to be largely imaginary. Unfortunately for all of humanity subject to his policymaking decisions, he’ll fit right in with Kissinger and his sorry array of pals.

Source: The Telegraph

Editor’s note: A $1bn yacht might be the ultimate symbol of excess, conspicuous consumption, and waste. But make it “hydrogen-powered” and suddenly it’s a symbol of virtue, or so the bottom-feeding press would have you believe (see an exhibit below if you can stomach it).

And at all that Gates did not even earn his fortune (that he is now using to help keep you in lockdown), but is a tax parasite owing all his ill-begotten wealth to a state-granted monopoly patent. These were rightfully abolished centuries ago, but for some reason when it comes to the bogus concept of “intellectual property” a “patent” can still be obtained that ensures the sovereign will expend its own resources to force subjects to pay what amount to taxes (“license fees”) to a private entity.

by Iain Davis, first published on 28th May 2019

Recently business man David Noakes was released from prison having served six months following his conviction on four charges relating to the manufacture, sale and supply of an unlicensed medicine.

(This article originally published on in-this-together.com. Republished in full with permission.)

Noakes pled guilty to all charges, including one of money laundering. This is something the MHRA and the mainstream media (MSM) have been very keen to highlight because it casts Noakes as a ‘real criminal.’

Money laundering is an automatically levied charge if anyone ever sells an unlicensed ‘medication.’ Pleading guilty to selling an unlicensed medication automatically makes you guilty of so called ‘money laundering.’ David Noakes is no BCCI executive.

Over 6 years Immuno Biotech made £7.6 million selling GcMAF. Out of that they paid a staff team of 27 including 4 research scientists, 7 doctors, 2 ultrasound staff, 4 nurses and admin staff for 6 years. They paid for the laboratories, staff travel (a significant expense) and accommodation. Any additional revenue they pumped back into GcMAF research and development. The CEO of GlaxoSmithKline earns approximately £6 million every single year.

The alleged medicine is not a synthetic manufactured pharmaceutical. It is actually derived from naturally occurring human protein. It is called ‘Gc Protein-derived Macrophage Activating Factor,’ or GcMAf for short. How and why GcMAF is being withheld from the public, despite an abundance of supporting scientific evidence, reveals a system of corrupt corporate control designed to profit from our sickness and death.

The scientific evidence clearly shows that GcMAF is potentially the most effective cancer treatment ever discovered. At David Noakes trial Judge Nicholas Lorraine-Smith made it clear that GcMAF was not on trial. He accepted that Noakes had acted out of a genuine desire to treat people; he noted that GcMAF had been instrumental in successfully treating people who had been written off by the medical profession and added that he was looking forward to GcMAF being made available to the public. He then sentenced David Noakes to prison.

Judge Nicholas Loraine Smith had little choice, and was compelled to make the required legal decision. He clearly felt uncomfortable and gave David Noakes just 15 months instead of the fourteen year sentence the Medicines & Healthcare Products Regulatory Agency (MHRA) were seeking. The difficulty he faced was highlighted when he stated, during the trial, that the court was not a court of morality but rather a court of law.

Clearly, in this case, the law is an ass. If the UK state recognised the codified British constitution then a jury could have annulled this statutory lunacy. However, through 800 years of lies and deception, the UK Parliament has unconstitutionally seized illegitimate sovereignty for itself and its statute laws. It was under this corrupt system the MHRA brought the case against David Noakes. When asked at the trial if he would do the same again David Noakes looked the Judge in the eye and said he would. He is a man who commands considerable respect in my opinion.

Under the 1939 Cancer Act it is illegal in the UK to advertise any cancer treatment which is not approved by the state. It is also illegal to offer any claimed cancer treatment, prescribe any claimed cancer treatment or offer any non-state sanctioned cancer treatment advice. I am not medically qualified, am not offering any medical advice and am not promoting GcMAF. I recommend you always seek qualified medical advice if you are ill. Rather, I am exposing what seems to be a rank injustice and questioning the system of cancer treatment approval and regulation in the UK.

The charges were brought against Mr Noakes, his team of research scientists, doctors, nurses and medical researchers at Immuno-Biotech, by the UK MHRA. David’s partner, and biomedical research scientist, Lyn Thyer, is due to be extradited to France to face similar charges. This at the behest of the French equivalent to the MHRA (the OCLAESP) who lobbied the EU to issue a European Arrest Warrant (EAW.)

Lyn has been found entirely innocent of all related charges in the UK and even the MHRA admitted she was guilty of nothing. Under EU law an EAW can only last a maximum of 60 days. At her previous extradition appeal hearing on 28th March 2019 the EAW had been in effect for approximately 700 days. The EAW is based upon charges simply copied from the original charges brought against David Noakes and are completely unrelated to Lyn Thyer. This copy and paste of charges was evidenced by the fact that the EAW charge sheet provided to Lyn had David Noakes’ case number on it.

At that hearing most observers noted that the Barrister, representing the French prosecutor’s, presented no evidence to support the extraditions request. This is understandable as, under UK law, Lyn Thyer is not guilty and the charges she faced weren’t hers, they related to David Noakes. As far as anyone knew, including the MHRA, there was no evidence at all against Lyn Thyer. Justice Supperstone then stated he would give a written ruling and adjourned the court. Consequently, based upon evidence which only Justice Supperstone has seen thus far, Lyn Thyer was informed that the extradition request had been granted. It is reasonable to assume that David Noakes will soon face a similar extradition request. However, at the time of writing Lyn is yet to be extradited, so there is hope sense will prevail.

In 2016 the UK parliament passed the Access to Medical Treatments (Innovation) Act. It states:

The purpose of this Act is to promote access to innovative medical treatments (including treatments consisting in the off-label use of medicines or the use of unlicensed medicines).

The clearly stated purpose of the Act is to allow responsible doctors to prescribe off label (using licensed drugs for innovative purposes) or unlicensed drugs, such as GcMAF, if it is considered by the prescribing Doctor to be beneficial. All Immuno Biotech GcMAF treatments were prescribed by qualified Doctors who thought prescribing it would be beneficial. They were right.

In response to the Access To Medical Treatments Act (Innovations) 2016 the MHRA issued guidance which stated that prescribers should first consider using a licensed medicine where possible; if that is not possible, then a licensed medicine off-label should be used, and only if neither of these are available should an unlicensed medicine be considered. Every patient selected for the GcMAF UK trials by Immuno Biotech had exhausted all licensed treatment options. In each case (for the UK trials) treatment had failed. Therefore it seems providing them with GcMAF was both legal and within MHRA guidelines.

However, European Law, in regard to EAW duration, and UK law, under the 2016 Act, can simply be ignored in the case of everyone connected to Immuno Biotech and GcMAF. In fact, it makes you wonder why we bother with UK law at all. Clearly it only applies to some people and is utterly ignored when it is inconvenient to the state, its agents or its corporate backers. Especially if the EU demand it.

Despite the appalling bias in the reporting of the case by the UK mainstream media (MSM), in reality Immuno Biotech were undertaking scientific research and clinical trials into the effectiveness of GcMAF. Apparently with very encouraging results. Technically Noakes broke the law because he sold some GCMAF to those who could afford it. He also gave away 25% of Immuno Biotech’s GcMAF, to those who couldn’t afford it, free of charge.

For reasons we’ll soon discuss, David Noakes knew it was pointless seeking a license from the MHRA to develop GcMAF. However, he reasoned that he and his team should be safe from prosecution. Firstly they had approval from the Guernsey authorities and had applied for and been given an import licence for GcMAF by the Guernsey Border Agency which they withdrew only after the MHRA allegations. All tests and scientific evidence showed that GcMAF was safe, it caused no known adverse drug reaction (ADR) and has never harmed or killed anyone. So he proceeded with the trials and subsequent distribution of GcMAF. He did so in the knowledge the MHRA hadn’t even admonished pharmaceutical corporations who had sold drugs which were proven to kill people.

Research of GcMAF is warranted.

In 2007 A study published in the New England Journal of Medicine found that the GlaxoSmithKline (GSK) diabetes drug Avandia increased the risk of heart failure by a minimum of 43%. The U.S Food and Drug Agency (FDA) subsequently acknowledged that an estimated 83,000 people had been killed by Avandia in the U.S. GSK were ordered to pay $3 billion in compensation.

Knowing this, in the UK, the MHRA recommended to U.K. doctors that they continue to prescribe Avandia ‘only to patients without a recognised heart condition’ and monitor patients taking Avandia more closely. The MHRA didn’t even criticise GlaxoSmithKline for marketing a drug which they knew to carry a significant cardiovascular risk, proven to be lethal. They eventually recommended its withdrawalthree years later. They didn’t provide any data on how many British patients it killed.

Therefore David Noakes considered that the benefits of proceeding with GcMAF research and development in the UK far outweighed what he saw as the minimal risk of MHRA disapproval. What he didn’t take into account was the corruption at the heart of the MHRA and their role as defenders of Big Pharma’s monopoly. His mistake was thinking that the MHRA would be consistent if they ever investigated Immuno Biotech.

Immuno-Biotech carried out extensive trials, publishing more than 30 peer reviewed papers. Approximately 11,000 people received GcMAF and the collected data consistently showed very promising results. The scientific laboratory research results were also consistent and encouraging.

Some of the success stories with GcMAF have been remarkable. For example the only 5 patients with terminal stage 4 pancreatic cancer, which is particularly deadly, were all treated successfully with GcMAF. The patients were chosen for the UK administered trials because they had stage 4 cancers (and other chronic or terminal illnesses.) All the cancer patients had been told by the medical profession that there was no hope. Treatment had failed and many were advised to put their affairs in order and prepare for the inevitable.

Following treatment with GcMAF, Immuno Biotech found that it ‘removed’ all cancerous tumours, with 75% of stage 4 cancer patients going on to live full lives for years. Unfortunately, for patients who had undergone chemotherapy the success rate was greatly reduced to 40% but for those who hadn’t it was above 80%.

Among many of note was a 60 year old woman with terminal stage 4 inoperable breast cancer. She was unlucky to be one of a 20% of breast cancer patients who possess a virulent cancer producing gene called the HER2 oncogene, for which there ‘was’ no known treatment. After 3 weeks of treatment with GcMAF she returned to her specialist who was amazed to find her cancer had reduced and was now easily operable. They removed the tumour but were even more stunned when they tested her to find the HER2 oncogene was clear. She went from Stage 4 inoperable cancer to completely cancer free in 4 weeks. A medical first, thanks it seems to GcMAF.

However, perhaps the most remarkable success was Teri Davis Newman. She had a genetic predisposition to contracting a particularly vicious form of ovarian cancer called peritoneal carcinomatosis which, unless diagnosed very early, in stage 2-4 is fatal in 100% of cases. Teri was told by her oncologist that she would be dead by November 2016. She had watched chemotherapy ravage her sister before she died horribly and declined the treatment.

Her insurance company would not pay for the GcMAF and so Immuno Biotech gave it to her free of charge and even paid the shipping costs. As of February 2019 Teri is still posting videos on YouTube. It seems peritoneal carcinomatosis need no longer be considered an automatic death sentence. Another apparent GcMAF medical breakthrough.

On the UK Government website there is an MHRA press release entitled “Notorious Noakes. £10M Guernsey GcMAF Crook Imprisoned.” This contains what appears to be a blatant lie:

There is no scientific basis for any of Noakes’ claims about the product.

Approximately 300 scientists, around the world, have published more than 140 peer reviewed scientific papers on GcMAF in so called reputable journals. The American National Library of Medicine, through its PubMed collaboration with the National Center for Biotechnology Information, has alone published 73 papers from 180 scientists spanning 8 different nations. The GcMAF used in these studies was predominantly provided by Immuno Biotech.

The scientific research shows that GcMAF appears to have six distinct attack mechanisms on cancer cells. It restricts and cuts off the blood supply to tumours (inhibits angiogenesis;) it stimulates the macrophages, the cells which attack cancer cells and promotes the destruction of cancer cells (phagocystosis;) it promotes apoptosis, cancer cell’s self-destruct mechanism; it reverts cancer cells ‘phenotype’ back to normal cells and it demonstrated the potential to reduce the ability of cancer cells to metastasise (in the petris dish.)

In addition, further peer reviewed scientific evidence demonstrated that GcMAF increases mitochondrial energy production (the biochemical batteries in all cells;) it improves human neuronal metabolic activity; counters the toxic effect of substances such as cadmium; it acts as an effective neuropathic pain killer and promotes neuropathic pathway growth (dendrils & neuritis.)

For example in 2014, by combining GcMAF with olive oil, Scientists at the Italian Department of Experimental and Clinical Biomedical Sciences were able to show a 25% tumour reduction per week for Stage 4 terminal cancer patients who had been told there was nothing more doctors could do. They concluded:

“These observations demonstrate that OA, GcMAF and NO can be properly combined and specifically delivered to advanced cancer patients with significant effects on immune system stimulation and tumour volume reduction avoiding harmful side-effects.”

In 2012, a team from one of the world’s leading cancer research centres, the Nagasaki Medical Center, studied the effect of GcMAF on tumours in mice with startling results. They found that by binding GcMAF to vitamin D (creating DBF-MAF) its impact on hepatocellular carcinoma (HCC) was marked. They stated:

“DBP-maf has at least two novel functions, namely, an anti-angiogenic activity and tumor killing activity through the activation of macrophages. DBP-maf may therefore represent a new strategy for the treatment of HCC.”

Researchers in Ohio from the Division of Basic Medical Sciences found that GcMAF combined DBP-MAF could stimulate bone marrow repair. Writing their conclusion in 2003 they stated:

The data suggest that DBP-MAF and the synthetic peptide represent therapeutic opportunities for the treatment of a number of bone diseases and skeletal disorders. Systemic administration could be used to treat osteoporosis and a number of other osteopenias, and local administration could be effective in fractures, bony defect repairs, spinal surgery, and joint replacement.

In 2005 a team from the Department of Peadiatrics and the Program in Women’s Oncology at Brown University in the U.S found that GcMAF derived DBF-MAF acts as a potent anti-angiogenic factor and inhibits tumour growth in vivo (tested on live subjects.) They concluded:

Understanding the cellular and molecular mechanisms of anti-endothelial activity of DBP-maf will allow us to develop it as an angiogenesis targeting novel drug for tumour therapy.

A year earlier, in 2004, a team of Japanese research scientists found that GcMAF based DBF-MAF could disrupt both angiogenesis (cut off blood supply to tumours) and promote apoptosis (cancer cell’s self-destruct mechanism.) It appeared to be particular effective in ‘removing’ pancreatic cancer tumours. This was later confirmed by the remarkable treatment of the five stage 4 pancreatic cancer sufferers by Immuno Biotech. The Japanese team wrote:

These results suggest that antiangiogenic therapy using angiogenesis inhibitors may become a new strategy for treatment of pancreatic cancer in the near future.

In 2010 a team from Kentucky working in the Department of Ophthalmology and Visual Sciences discovered that GCMAF derived DBF-MAF exhibited a potent effect on prostate cancer tumour cells and inhibited their migration. They concluded:

These studies show strong inhibitory activity of DBP-maf on prostate tumour cells independent of its macrophage activation.

These are just some of more than 140 peer reviewed, published scientific papers which attest to the potential of GcMAF to become a game changer in cancer treatment. There are nearly 800 GcMAF papers listed on Google Scholar alone. There is absolutely no doubt at all about the wealth of scientific evidence which indicates that GcMAF has the potential to revolutionise, not just cancer treatment but a whole range of treatments for terminal and life limiting illnesses. Certainly significant further research is warranted and there is every reason to hope that GcMAF could make death from most cancers a rarity.

So why have the MHRA and the UK state seemingly decided to mislead the public by claiming there is no scientific evidence to support David Noakes’ claims? Instead of supporting his team they have done everything possible to silence Noakes and Immuno Biotech Laboratories (IBL). They have worked with the MSM to rubbish IBL’s research and to hide the scientific evidence which obviously indicates the enormous, lifesaving potential of GcMAF.

They have destroyed IBL laboratories, made false claims about their research methods, denied unequivocal scientific evidence, imprisoned Noakes and his leading research scientists, hounded him and his loved ones through the courts, are intent upon seizing all his assets and will extradite Lyn Thyer to France where she can expect to spend years on remand in some of the worst prisons in Europe. All because they researched, developed and gave to suffering people what could well be the most effective cancer treatment ever discovered.

But what is truly despicable is that when they shut down Immuno Biotech and seized all their GcMAF, the IBL team were actively treating 200 patients. These people were winning their battle against cancer having previously been told there was no hope. The MHRA decided they didn’t deserve that chance. The MHRA withheld their GcMAF treatment and effectively condemned 200 people to death. The Immuno Biotech team, who knew these people well, had to watch each of them pass away, with devastating effects both on the families and the Immuno Biotech team.

The drugs sold to us by large pharmaceutical corporations (Big Pharma) frequently kill hundreds of thousands of people. In the U.S. The Food & Drugs Administration (FDA), until recently, reported U.S deaths from Adverse Drug Reactions (ADR’s.) In 2015 there were over 2 million ADR’s resulting in 100,000 deaths with ADR’s the 4th leading cause of death in the U.S.

The FDA equivalent in the UK, the MHRA, don’t bother reporting these statistics but with a population 20% of the size of the U.S it would be reasonable to assume that ADR’s affect in the region of 400,000 people annually, resulting in approximately 20,000 deaths. This estimate was corroborated in 2018 when the NHS admitted that the ‘overprescribing’ of prescription medication, and other ‘drug errors,’ contributed to more than 22,000 deaths in the UK every year.

In response, a few months later, a group of 6 eminent doctors including Sir Richard Thompson, the former President of the Royal College of Physicians, and leading heart specialist Dr Aseem Malhotra, publicly stated the need for a ‘Chilcot style inquiry’ to investigate the tactics used by Big Pharma to pressurise the NHS into prescribing drugs patients don’t need. Leading to a situation where prescription drugs are the UK’s third largest cause of death, after Cancer and Heart disease.

There is no doubt that the pharmaceutical giants frequently act with criminal negligence. A 2018 report by the U.S consumer rights group PublicCitizen showed that between 1991 and 2017 Big Pharma paid out over $38.6 billion in criminal and civil penalties. That was just in the U.S.

While these sums are unimaginable for most of us they mean little to an industry that generates nearly $1.2 trillion annually. The odd multibillion dollar lawsuit for killing people here and there is little more than an occupational hazard for Big Pharma and well within their profit margins.

Big Pharma is a corporate venture that has absolutely no vested interest at all in curing disease. They became acutely aware of the problem of cures in 2015 when Gilead Sciences (GILD) developed a 90% effective cure for Hepatitis C.

Initially the $12.5 billion in revenue from the GILD cure was welcomed. However, the problem with a cure, from an investment perspective, is that it cures people. The former Hep C patients no longer needed any treatment, and revenues fell off a cliff as more and more people didn’t require medication. What was even worse were the rapidly diminishing numbers of people spreading infection, creating fewer and fewer new customers.

The global investment firm Goldman Sachs are one of the world’s leading investors in the pharmaceutical industry. They were concerned about the potentially catastrophic financial effects of curing people. They saw that advances in medical science threatened to make people well and thus reduce their return on investment (ROI.) In 2018 they issued their report The Genome Revolution. In it they questioned if curing disease was sustainable from a business model perspective. Their analyst’s conclusions make horrifying reading.

The potential to deliver ‘one shot cures’ is one of the most attractive aspects of gene therapy, genetically-engineered cell therapy and gene editing. However, such treatments offer a very different outlook with regard to recurring revenue versus chronic therapies …

GILD is a case in point, where the success of its hepatitis C franchise has gradually exhausted the available pool of treatable patients …

In the case of infectious diseases such as hepatitis C, curing existing patients also decreases the number of carriers able to transmit the virus to new patients, thus the incident pool also declines … Where an incident pool remains stable (eg, in cancer) the potential for a cure poses less risk to the sustainability of a franchise.

While the Machiavellian logic of this analysis may be difficult for most to stomach, it makes sense from a business perspective. The ideal patient is never cured and cures are to be avoided wherever possible. Cancer treatment is fantastic because the ‘incident pool is stable’ and there is ‘less risk to the sustainability of the franchise.’ The last thing Big Pharma wants to see is anything that looks remotely like a cure for cancer.

Recently scientists at the new Centre for Cancer Drug Discovery (CCDD) announced that they were researching drugs which could make cancer a long term manageable condition. Meaning you can live with cancer a lot longer providing you keep taking, what will undoubtedly be, hugely expensive Big Pharma medication.

These lifelong cancer sufferers will represent an extremely stable ‘incident pool’ providing excellent ‘sustainability for the franchise.’ The CCDD is a project of the Institute for Cancer Research who are partners of the pharmaceutical giant Merck, among others.

The problem with GcMAF, from a corporate perspective, is that it looks like it might deplete the ‘incident pool’ dramatically. Not only that, it is relatively cheap at only £380 for a round of treatment. This is nowhere near as lucrative as the chemotherapy and other cancer drugswhich vary between £5000 and £40000 per round.

We have all probably lost people we love, or care for, to cancer. So ultimately ‘the incident pool’ does decline. That is why end stage cancer treatments are hugely expensive. Maximising profits to the very end is an essential component of the pharmaceutical corporation’s profit model. As patients and families become more desperate, the opportunities for profit escalate reciprocally.

Cytoxic chemotherapy kills cancer cells but it doesn’t discriminate very well. It also kills healthy cells. This is perhaps unsurprising, given that chemotherapy was developed from the mustard gas that killed tens of thousands on the WWI battlefields. Things have improved because Big Pharma has developed a panoply of very expensive drugs which counter the vicious side effects of the very expensive chemotherapy.

An Australian study looked at 5 year cancer survival rates. These are continually improving and currently stand at more than 60%, though some cancers, such as pancreatic, continue to have very high mortality rates. The study considered the various treatments that contributed to 5yr survival rates. These included surgery, radiotherapy, hormonal therapy, immune therapy and chemotherapy. They then looked at the comparative effectiveness of these treatments for more than 15,000 survivors. They found that chemotherapy contributed to less than 3% of the overall 5 year survival rates. They stated:

As the 5-year relative survival rate for cancer in Australia is now over 60%, it is clear that cytotoxic chemotherapy only makes a minor contribution to cancer survival.

We need to be careful how we interpret these results. Many people have alleged them to show that chemotherapy is 97% ineffective. This isn’t the case. All it shows is that the effectiveness of chemotherapy is almost certainly overstated.

Further studies do suggest the general ineffectiveness of chemotherapy. A joint 2015 meta-analysis study between the University of Melbourne, Adelaide and The Mayo clinic in the U.S found that chemotherapy appeared to be effective in less than 8% of cases for stage 3-4 patients. So it is fair to say that it was more than 92% ineffective in this study of nearly 3000 cases.

Therefore, if we consider both that chemotherapy only appears to contribute minimally to 5 year survival rates, mostly for people who were diagnosed earlier, and it is more than 92% ineffective for treating late stage cancers, then the picture that emerges is one of a hugely expensive (profitable) treatment with highly questionable efficacy.

Analysis by the market research company Transparency Market Research predicts a U.S cancer treatment industry worth an estimated $155.6 billion per annum by 2025. This represents a 6 – 7% compound annual growth rate (CAGR) over the next 5 years or so. The CAGR for Chemotherapy drugs is even better and is projected to be nearly 12% between 2018 and 2023. A fantastic opportunity for venture capitalists, providing no idiot ruins it all be actually curing cancer.

The cost of chemotherapy is the single largest cost faced by the NHS taking almost 10% of the entire central budget. In 2016 this amounted to £1.4 billion ($1.8 billion.) With an estimated 8% cost increase per annum, no wonder the CAGR is excellent.

Professor Dolores Cahill, renown microbiologist from Ireland and an active supporter of the anti-lockdown and anti-mRNA vaccine, explains why this vaccine is worse than the disease it claims to prevent. Listen in her own words: