Zionist Made2Happen Disasters: The Hidden Truth Behind The News

-Peter Eyre – 25/8/2014
Middle East Consultant – Political Analyst – Investigative Journalist – Broadcaster

(article extracted from Jeans' blog ,
http://jhaines6.wordpress.com/2014/08/25/the-new-world-orderwho-scam-what-they-want-you-to-believe-by-peter-eyre/)

For those of you who find it hard to read single-word lines, here's the full article text minus the graphics. For the original complete post, goto

http://eyreinternational.wordpress.com/2014/08/25/the-new-world-orderwho-scam-what-they-want-you-to-believe-2/

The Hidden Truth Behind The News

The New World Order / WHO Scam & What they want you to believe!!

Can of worms How to open a New World Oder “Can of Worms”

Eyre International – Bringing You The News No One Else Wants To Bring You The Hidden Truth Behind The News Australian Government almost forcibly pushes the HPV vaccines on young boys as well as girls Part 7 (Final)

Or a World Health Organisation “Hornets Nest”

So what have these New World Order “Imbeciles & Morons” introduced to the world since their inception?

HIV/AIDS – Various “False Flag Flue Vaccines – Autism via MMR vaccines – HPV Vaccine(unsafe/unproven) that can create infertility or even death – Anthrax – Ebola and their total misguided analysis of Cancer.

What do they hope to achieve and what do they gain from their genocidal plans?

1 – Agenda 21 and a massive reduction in the worlds population by whatever means.

2 – Incredible wealth for their own pharmaceutical empire.

Their deadly illegal trade/use of Weapons of Mass Destruction/Chemical & Biological & Chemical Warfare

How do they do it?

Create a “False Flag Fear” such as Swine Flu or Ebola then call it an pandemic and create a vaccine to tackle the alleged outbreak, Introduce a toxic adjuvant into the vaccine or unhealthy ingredient or germ, by-pass normal pharmaceutical protocol by rushing them onto the market (especially when it has not been tested on humans or has not followed normal safety protocol) and then reap in the billions of dollars in sales!!!

What would happen if someone independently challenged the war lords of the pharmaceutical industry and fed you more concrete information that they are deceiving you and causing our children harm?

Before moving forward on this topic we must also understand that our respective governments and Departments of Defence are contaminating our entire planet with millions upon millions of radioactive nana particles in breach of the Geneva Convention in their constant use of WMD’s

Almost every weapon used on the battle field since the mid 70’s contain depleted uranium (DU) that has a half life of 4.5 billion years, cannot be cleaned up and contaminates innocent civilians (both on and off the battlefield), our own troops and the world beyond as demonstrated in my own distribution chart.

What if it could be proven that “Cancer Research” is a scam or that MMR vaccines does cause autism etc?

Lets first look at cancer and what some good genuine experts have done in order to close the door on cancer once and for all.

Here is one such article with some pretty convincing evidence:

Thoughts On Breast Cancer Awareness Month

by LAWRENCE BROXMEYER M.D.

10-05-2009

Hodgkin’s cancer under attack

Dr. Virginia Livingston

Momentum builds

Recognition

US studies take hold

Focus on breast cancer

The single most convincing study of how bacteria causes cancer

The politics of cancer

Parallels with plant cancer

Seibert rules out contaminants in the cancer germ

Experimental medicine for the masses

White Knight

BCG

Livingston’s legacy

Conclusion

[INTRODUCTION BY ALAN CANTWELL, M.D.: Lawrence Broxmeyer MD presents a landmark article on BACTERIA as causative (and suppressed) agents in cancer! A colleague of mine (an Internist) has written an excellent HISTORY (along with dirty medical politics) concerning the cancer microbe work.......that is, the evidence showing BACTERIA as being heavily implicated in the cause of cancer.

This continuing research, now dating back a century, has been SUPPRESSED by the medical establishment for many decades, presumably because the discovery of bacteria in cancer would threaten the multi-trillion dollar worldwide cancer INDUSTRY.

As you probably know, the cancer microbe, and its implications in human health and disease, has also been my life's work. Dr. Broxmeyer's report is a bit long, but I think anyone who has more than a passing interest in the cause of cancer, will find this article informative. By the way, the late Virginia Livingston MD was my mentor in this cancer research.] (10-7-09) The word ‘cancer’ is of Latin derivation and means “crab”.

Today cancer “cure” is a vast industry.

But by the turn of the 20th Century organized medicine had come to the conclusion that it was not a matter of whether infectious disease caused cancer, but which one. For over two hundred years a cancer germ had been discovered and rediscovered, named and renamed, each scientist adding to the knowledge, but to no avail.

Then, in 1910, certain American medical powers did a 180-degree rotation, deciding that cancer was not caused by a microbe, and that anyone who thought otherwise was a heretic, a charlatan or a quack. But Dr. Virginia Livingston and her network were none of the above, their meticulous peer-reviewed research and publications, done at the height of US post World War II technology.

And Dean Burk, Head of Cell Chemistry at the NCI went so far as to say that Livingston’s cancer germ was as real and certain as anything known about cancer. Researcher, MD Alan Cantwell Jr. grew up thinking that all germs responsible for the important diseases were supposed to have already been discovered. But much to his dismay, he found one that was left out: the cancer germ.

Cantwell already knew that for finding this, Livingston had already been branded by traditional medicine, leaving what he thought to be perhaps the major discovery of the 20th century largely discredited. The striking analogy between cancer and tuberculosis was noticed long before the tubercle bacillus was discovered.

In 1877, Sir John Simon clearly pointed out the similarity and in fact argued very strongly in favor of a microbial origin for cancer. But Simon’s vindication would have to wait for Livingston’s germ, which although tuberculosis-like, was not tuberculosis but an atypical form of this mycobacterium, melded from the mycobacterium and other related Actinomycetales.

Had medical science, and the powers that be, spent as much time in investigating and destroying Livingston’s germ as they did in attacking her and those around her, cancer might be curable today.

Hodgkin’s cancer under attack

When Virginia Livingston was a student at Bellevue Medical College her pathology teacher mentioned, rather disparagingly, that there was a woman pathologist at Cornell who thought Hodgkin’s disease (a form of glandular cancer) was caused by avian tuberculosis [1].

This lady had published, but no one had confirmed her findings. Afterwards, Livingston compared slides of both. In Hodgkin’s, the large multinucleated giant cells were called Reed-Sternberg cells. They were similar to the giant cells of tuberculosis, which formed to engulf the tubercle bacilli. Livingston stored away in her memory that this lady pathologist was probably right but she would have a difficult time in gaining acceptance.

By 1931, Pathologist Elsie L’Esperance was seeing ‘acid fast’ tuberculosis-like bacteria riddling her Hodgkin’s cancer tissue samples. And that germ, once injected into guinea pigs, caused them to come down with Hodgkin’s too, fulfilling Koch’s postulates. L’Esperance brought her stained slides to former teacher and prominent Cornell cancer pathologist James Ewing. Ewing initially confirmed that her tissue slides were indeed Hodgkin’s.

But when he found out that her slides came through guinea pig inoculation of the avian (fowl) tuberculosis she had found in humans with Hodgkin’s, Ewing, visibly upset, said that the slides then could not be cancer.

It betrayed his checkered history of high-placed medical politician. In 1907, you could have approached Dr. James Ewing about a cancer germ, and he would have embraced you over it. At that time, both for he and the rest of the nations medical authorities, it was not a question of whether cancer was caused by a germ, but which one. Was not it Ewing, at one time, who had proclaimed that tuberculosis followed Hodgkin’s cancer “like a shadow”?

But shortly after, James Ewing, “the Father of Oncology”, sent a sword thru the heart of an infectious cause of cancer with “Neoplastic Diseases” [2], becoming an ambitious zealot for radiation therapy with the directorship of what would one day be called Sloan Kettering squarely on his mind. His entry lay in prominent philanthropist James Douglas. A vote for Ewing, Douglas knew, was a vote for continued radiation and James Douglas began sizeable uranium extraction operations from Colorado mines through his company, Phelps Dodge, Inc. [34].

Soon Sloan became known as a radium hospital and went from an institution with a census of less than 15% cancer patients, separated by partition, lest their disease spread to others, to a veritable cancer center. But the very history of radiation revealed its flaws, and by the early 1900s nearly 100 cases of leukemia were documented in radium recipients and not long thereafter it was determined that approximately 100 radiologists had contracted that cancer in the same way [3].

Still, Ewing, by now an Honorary Member of the American Radium Society, persisted.

Elise L’Esperance was anything but alone in linking Hodgkin’s to a germ called Avium or fowl tuberculosis. Historically Sternberg himself, discoverer of Hodgkin’s trade-mark Reed Sternberg cell, believed Hodgkin’s was caused by tuberculosis. Both Fraenkel and Much [35] held, as L’Esperance, that it was caused by a peculiar form of tuberculosis, such as Avium or Fowl tuberculosis, and of all the cancers, debate over the infectious cause of Hodgkin’s waxed the hottest.

Into this arena L’Esperance stepped in 1931, with few listening. She would publish Studies in Hodgkin’s Diseases [4] in an issue of Annals of Surgery. It proved to be the one legacy that no one, not even Ewing, who would soon die from a self-diagnosed cancer, could take away.

Dr. Virginia Livingston

“Our (cancer) cultures were scrutinized over and over again. Strains were sent to many laboratories for identification. None could really classify them. They were something unknown. They had many forms but they always grew up again to be the same thing no matter how they were cultured. They resembled the mycobacteria more than anything else. The tubercle bacillus is a mycobacterium or fungoid bacillus.”

– Virginia Livingston, 1972

Virginia Wuerthele-Caspe Livingston was born in Meadville, Pennsylvania and went on to obtain impeccable credentials. Graduating from Vassar, she received her M.D. from N.Y.U. The first female medical resident ever in New York City, with time Livingston became a Newark school physician where one day a staff nurse asked medical assistance.

Already diagnosed with Reynaud’s syndrome, the tips of this nurses fingers were ulcerated and bled intermittently. Livingston diagnosed Scleroderma. But upon further examination there was a hole in the nasal septa, something that Livingston had previous seen in the mycobacterial diseases TB and Leprosy.

So Livingston approached dermatologist Eva Brodkin and a pathologist

for confirmation, all the while convinced that mycobacterial infection was causing the Scleroderma. She then preformed cultures from a sterile nasal swab mycobacteria appeared, everywhere [1]. Injected into experimental chicks and guinea pigs, all but a couple died. Upon autopsy, the guinea pigs had indeed developed the hardened skin patches of Scleroderma. . . some of which were cancerous.

Momentum builds

Livingston, now possessed, solicited fresh sterile specimens of cancer from any operating room that would give them to her. All cancer tissues yielded the same acid-fast mycobacteria. New Jersey Pathologist Roy Allen confirmed her findings. Livingston and Allen then found that they could actually differentiate malignant from benign tissue by their mycobacterial content [5].

But still the explanation for why the cancer germ showed so many different forms was elusive.

Try as she might, part of Virginia Livingston’s problems in an American validation of her multi-shaped cancer germ lay firmly entrenched in the history of medicine, especially in the constantly changing field of microbiology. Louis Pasteur could handle being quickly rushed off a Paris Academy of Sciences podium to escape harsh reaction to his suggestion that children’s milk be boiled first, but he could not tolerate his rival Pierre Bechamp’s statement that a single bacteria could assume many, many forms.

On his deathbed, Pasteur was said to have changed his mind when he said: “The terrain is everything”, meaning the culture or milieu that bacteria grew on or in could change their shape or characteristics. But it was too late and even today, most conventional microbiologists deny the existence of such form changing (or pleomorphic) germs.

Robert Koch, Father of Bacteriology and discoverer of tuberculosis, could have helped. When he first worked with the bacteria anthrax, he noticed that anthrax’s classical rod shape became thread-like inside the blood of laboratory mice. And then, after multiplying, they changed again, into the same assumed spore-like forms he later documented in tuberculosis as well.

Aware of what she faced, yet undismayed Livingston methodically went about proving cancers true cause. First in her line of attack were the long suspected and well-publicized tumor agents of Rous, Bittner and Shope. By photomicrographs, Livingston and her group demonstrated acid-fast mycobacterial forms in each of these so-called “viral” cancers. This included the famed Rous chicken sarcoma.

Early on, Virginia Livingston had decided that she needed help in validating her cancer germ and nobody knew the shapes and staining capacities of mycobacterial-related germs better than Dr. Eleanor Alexander-Jackson of Cornell.

As far back as 1928, Eleanor Alexander-Jackson, bacteriologist, had discovered unusual and to that point unrecognized forms of the TB bacillus, including its filterable forms. By 1951, Alexander-Jackson was considered the expert TB microbiologist at Cornell.

In the same year, another American, H.C. Sweany proposed that both the granular and other forms of tuberculosis that passed thru a filter caused Hodgkin’s cancer [6]. This was subsequently supported by studies by Mellon, Beinhauser and Fisher [7,8]. Mellon prophetically warned that tuberculosis could assume both its characteristic red acid-fast forms as well as blue nonacid-fast forms indistinguishable from common germs such as Staphylococci, fungi and the Corynebacteria and that this would surely perplex modern microbiologists.

When organized medicine choose to ignore these studies, Jackson warned that a so-called cure for TB could be as short-lived as it took classical TB rods, for the moment gone underground as a nonacid-fast form, to resurface one day and spring back towards destruction. Although American medicine had no serious time for Alexander-Jackson or her discoveries, it would not disturb her for as long as she focused on tuberculosis and its cousin, leprosy. But when her focus shifted towards Livingston’s cancer germ, it would move to destroy her. She simply posed too great a threat.

Recognition

By December of 1950 Livingston, who would go on to write over 17 peer reviewed articles by the end of her career, wrote, together with Jackson and four other prominent researchers, what still stands as a milestone on the infectious nature of cancer [9].

At the AMA’s 1953 New York exhibit, participants interest was particularly riveted towards an exhibit of Livingston’s cancer germ, live. The press, muzzled by Sloan Kettering’s head, Cornelius Rhodes, was not allowed to interview or report on this exhibit. Above, the cancer germs seemed indestructible, surviving a five-day experience of intolerable heat from closed-circuit microscopy [1].

As Livingston and Jackson’s work on the cancer germ became more and more convincing, her opponents surfaced and became more and more vocal.

Also with recognition, came visitors. One a pathologist from Scranton, Dr. George Clark, told Livingston he had cultured Dr. Thomas Glover’s famed cancer germ from human cancer and developed metastasizing tumors in animals from it.

Clark assured Livingston that Glover was on to the same bacterial pathogen that she was. For more than two hundred years, the same organism had been discovered and rediscovered, named and renamed, each discoverer adding to what was known about the cancer germ, but thus far to no avail.

US studies take hold

Clark knew Glover as part of an investigative team of the US Public Heath Service headed by George W. McCoy in 1929. Glover had just become too well known to be ignored. His cancer serum was working.

Much was at stake. The Country was already committed to the idea that cancer could not possibly be an infectious disease, and Glover was saying that he had already isolated the cancer germ.

Actually, he had not, but few would believe that it was really his young, tobacco-chewing assistant, Thomas Deaken who had isolated it. Deaken worked his way up New York’s health and hospital system from the most menial positions to laboratory assistant. With neither formal medical or scientific training, this laboratory assistant nevertheless learned laboratory protocol [10].

Incredibly Deaken engineered a geranium based culture medium, managing to grow out acid-fast, tubercular bacteria. Then he inoculated mice and dogs, producing cancer with metastatic spread in every case [10]. Sometime between 1917 and 1918 Thomas Daeken, laboratory assistant, produced a specific anti-cancer sera by injecting horses with the human cancer germ. Moreover, the sera worked whether in prevention or cure of his cancerous laboratory animals. But Glover had come to the point where he needed someone to lend credibility to his work, and that someone, came in the form of Dr. Thomas J. Glover of Toronto.

It will always be to Glover’s credit that he saw the importance and application of Deaken’s work from day one. A contract was quickly drawn up and executed. Glover rushed back to open a Canadian cancer clinic in Toronto. The serum worked in many but not all cases; but as Glover’s reputation grew, so to did the interest in him of Canada’s organized medicine. A subpoena giving him 21 days to submit a full presentation of his treatment was issued. But Glover was not cooperating. Glover was in trouble and would soon be chased out of Canada [10].

By 1926, and now in the US, Glover published Progress in Cancer Research, presenting over 50 cases, most of which went into remission with Glover’s Serum [11].

It sparked additional notoriety, both here and abroad. In 1929, Livingston’s friend Dr. George Clark joined Dr. George McCoy, then head of the Hygienic Lab of the US Public Health Service. Their intended destination: Glover’s laboratory, now at New York’s Murdock Foundation. Glover was under investigation and McCoy wanted him to repeat his work, this time under Health Service surveillance and in Washington.

Glover complied, and he and his team went to the nations capital to prove their case at what was to one day become the National Institute of Health. McCoy, the investigator, impressed by Glover’s work, rather than come down on Glover, instead issued a 1937 letter to Surgeon General Parran, which spoke in glowing terms of the great importance and significance of Glover’s cancer findings.

Soon thereafter, McCoy was abruptly and mysteriously replaced by Dr. R.H. Thompson. Parran, a product of organized medicine, had a definite agenda. The question before him was whether to publish Glover’s now finished Washington report or not and Parran, despite continued committee approval, was not about to, sending Glover into a cold rage which ended with him walking away from Washington to publish independently.Meanwhile, Glover’s serum, which had helped and saved so many was subjected to cursory animal studies and a review without clinical trials before being condemned by Government agencies.

Glover would eventually return to Canada, but he would never again answer questions as to just what had happened in America.

Focus on breast cancer

Virginia Livingston now went specifically after breast cancer. Thirty sterile cancerous breasts were transported from operating room to lab.

Cancers were isolated from each breast and when axillary tissue from under the arm was supplied, the cancerous portion was cut from this too. Livingston and Jackson found the cancer germ everywhere, and in the case of underarm glands, even when the pathology report was negative, the cancer microorganism surfaced [1].

Champion of toxic chemotherapy, Cornelius Rhoads replaced Ewing at Sloan. Rhoads, head of chemical warfare during the Korean war, was deeply committed to chemotherapy and the huge grants it brought from the pharmaceutical industry.

It is poorly recognized that the chemotherapy or “chemo” used against cancer began as a weapon of mass destruction par excellence [12]. When the Axis folded, nitrogen mustard, declassified, first came under real medical scrutiny for cancer. Initially evaluated for lymphosarcoma in mice, human studies soon followed as more and more variants of nitrogen mustard were concocted and tried [12].

Other related classes of chemotherapeutic agents followed and so did their repercussions. Most had the potential to cause a second entirely different cancer [13]. Even tamoxifen for breast cancer was associated with a two to three-fold increased risk of cancers of the lining of the uterus (endometrial), some of which were high grade with a poor forecast [14].

Nevertheless, Cornelius Rhoads remained committed to the treatment, and at the same time prepared a series of major roadblocks to stop Livingston.

In 1950, he barred her from presenting her paper on the cancer germ at the New York Academy of Sciences by discrediting Irene Diller, the symposiums sponsor, chief-editor of the respected journal Growth, and a prominent cancer researcher. Diller, like many, had accepted a gift from a pharmaceutical house at one point. Livingston came across Diller in a Life Magazine article which talked about a Philadelphia cancer researcher who was observing strange fungus-like filaments protruding from cancer cells. Livingston and Alexander-Jackson convinced her that her fungal forms (the prefix myco in mycobacteria denotes a germ with fungal properties) were part and parcel of the cancer microbe, and that crucial to its identification was acid-fast staining.

Dr. Eleanor Alexander-Jackson’s elation over the groups infectious breast cancer findings came to an abrupt halt when she was informed by her private physician Frank Adair that she too had it. A radical mastectomy was done at Sloan on Adair’s advice.

While anxiously waiting for the outcome, Dr. Virginia Livingston heard her name paged on Sloan’s overhead. Rhoads wanted to speak to her regarding Jackson’s ongoing surgery. It was urgent. Alexander-Jackson was still in the operating room and the radical mastectomy had been done. In Rhoads office, the two adversaries faced off. incredibly, Rhoads was after permission to go after a cancerous lymph node deep in the middle of Eleanor’s chest. Livingston bristled.

“We have been looking for a tumor such as she has.” said Rhoads.

Apparently a radical was not enough. He was seeking permission to try a new surgical technique which went after the deep chest node.

Livingston had had enough. Just the thought of the cruel, disfiguring procedure made her sick. “Not on your life.” She shot back, as she left [1].

The single most convincing study of how bacteria causes cancer

By 1965, Edith Mankiewicz, Director of labs at Montreal’s Royal Edward Chest Hospital and assistant professor of bacteriology at McGill, by examining human cancer tissue, established mycobacteria-like germs inside cancer [15]. In the bibliography of one of her landmark papers is reference to a personal communication with Dr. Eleanor Alexander-Jackson. One of the cancers under Mankiewicz’s trained eye was lung cancer. Lung cancer,or bronchogenic cancer, was first reported in the nineteenth century at a time when it was practically unknown-while mycobacterial disease of the lung, primarily tuberculosis, was so rampant as to be called ‘white plague’ or in certain circles: ‘captain of the men of death.’ By the middle of the seventeenth century, one in five deaths was due to tuberculosis and at the end of the nineteenth century, there was fear that it would destroy the very civilization of Europe. So difficult was it to differentiate tuberculosis from the newly discovered bronchogenic cancer that it was only after cases first mistakenly diagnosed as lung cancer were operated on that the benefits of surgical resection of tuberculosis were recognized [16].

Mankiewicz not only showed the cancer germ in malignant tissue but significantly demonstrated how it probably evolved from tuberculosis and related microorganisms when some of the viral phages that lived in them jumped germs, bringing genetic materials which altered the target germs virulence and made them drug resistant.

In fact beneath her microscope lay a pictorial of how the cancer germ emerged from TB-like bacilli to create pre-malignant change in mammalian tissue [15].

By 1970, Sakai Inoue, a PhD from Maebashi, Japan and Marcus Singer, a doctor at Case Western’s Developmental biology, completed the single most convincing study of how bacteria cause cancer altogether, with TB-like mycobacteria. Supported by grants from the American Cancer Society and the National Institute of Health, their study used cold-blooded animals, namely the newt or salamander and the frog. But similar studies showed its applicability to mice [17] and humans [18,19]. Inoue:

“An organism similar to the mycobacterium Described here has been isolated and cultured from tumors and blood of tumerous mammals, including man, and when injected into mice and guinea pigs, has been reported to yield a chronic granulomatous disease, neoplasm (cancer), or some intergrade.”

– Inoue and Singer, 1970

Back in the spring of 1953, Sakai Inoue noticed an adult salamander with a hard mass on its stomach. He removed the mass, which turned out to be malignant. Then he injected tissue from the mass into healthy animals. Again, cancer developed.

In the work that followed, Inoue and Singer, from electron micrographs, knew that bacteria were involved, bacteria which stained acid-fast…mycobacteria [20]. Inoue inoculated three other types of mycobacteria, into healthy animals. All came down with cancer, something that did not happen when other germs such as staphylococcus or streptococcus were used. Amazingly Inoue and Singer even noted regressions in some of the cancers, especially if very dilute solutions of the germs were used to initiate them. Furthermore, since cancers stemming from ‘carcinogens’ were structurally identical to mycobacterial induced cancers, the investigators results suggested that such ‘carcinogens’ might merely be factors that activate preexisting infection. The phages inside mycobacteria are viruses known to be activated by carcinogens such as UV light and chemicals [21].

Mankiewicz, five years previously, had shown that these phages, once activated, could cause pre-malignant changes in mammalian tissue [15].

Sakai Inoue and Marcus Singer’s study should have once and for all convinced Virginia Livingston’s opponents of the veracity of her results, and that she was not mistaking common contaminants such as staph. or strept. for the cancer germ. . .but it did not.

The politics of cancer

It was public knowledge in early 1951 that the Black-Stevenson Cancer Foundation intended to award two huge Black grants of $750,000 towards

cancer research and that the first would go to Livingston’s group at Newark’s Presbyterian; with an equivalent amount to go to The Memorial Center for Cancer (now Sloan-Kettering), which Rhoads headed. The trustees having already decided this, the actual allocation was left in the hands of Newark lawyer Charles R. Hardin, but fate intervened.

Livingston:

“Hardin, the lawyer in charge of allocation, soon would lie dying of cancer at Memorial and while still alive was prevailed upon by design of Rhoads to sign a paper giving Rhoads power over how Presbyterian’s grant was to be spent. And that wasn’t going to include further research towards an infectious cause for cancer.” — Livingston, 1972

Still Rhoads was not finished. Livingston, already world-recognized, took her cancer microbe and a guest named George Clark to Rome’s Sixth International Congress for Microbiology, a trip paid for by her husband’s firm as a consultant to British industry. In Rome, Livingston met Emy Klieneberger-Nobel at the Lister institute. Klieneberger-Nobel was a pioneer uncovering bacteria without cell walls which led them to assume many forms [32]. She called them ‘L-forms’ in deference to the Institute at which she worked. Her exploration also covered bacteria with cell-wall breeches. In either case, the resulting germs, called ‘cell-wall-deficient’ assumed many forms (pleomorphic). Livingston immediately saw Klieneberger’s work as clearing a large part of the confusion over her many-formed cancer germ.

Livingston’s trip to Rome’s Congress of Microbiology was punctuated by a stop to visit von Brehmer in Frankfort. Von Brehmer’s vaccination techniques, long respected throughout Europe, were now licensed by the German government.

During the war, Wilhelm von Brehmer’s scrimmage with the Nazi medical establishment went right to the top. Severely criticized for saying that cancer was an infectious disease, the struggle eventually found its way to Hitler himself, who, puzzled, yet interested, ordered an inquiry on the matter at the 1936 Nuremberg Party Conference. Subsequently, the committee formed came down hard on von Brehmer’s views. Nevertheless, unperturbed, he somehow persisted into the legendary status he now maintained.

Big names began to join the conference, including Nobel Laureates Fleming and Waksman. By the time Virginia Livingston returned to the States, the Rome conference had been highlighted by several news services. Beginning with the New York Times and The Washington Post, other papers quickly followed suite: the cancer germ had been found. Reaction quickly followed. At The New York Academy of Medicine, spokesman Iago Gladston, fresh from executive session, held his own sort of news conference:

This is an old story and it has not stood up under investigation. Microorganisms found in malignant tumors have been found to be secondary invaders and not the primary cause of malignancy. Livingston, 1972 Livingston returned to Newark. Her Chief, James Allison, contacted her with the bad news. Since they had lost Black-Stevenson funding, he wanted her to close up Presbyterian’s research and move back to Rutgers’s home campus in distant New Brunswick. And in still another cost-cutting gesture, she was informed that her close friend and associate Eleanor Alexander-Jackson would have to go. Shocked, Livingston made arrangements to leave Rutgers altogether. Barely unpacked from Europe, Livingston’s husband would now be hounded by the IRS regarding where they got the funds for the European trip.

Someone had implied the money came from his wife’s grants. This did not bear out and the couple demanded to know who had instigated the inquiry. “Someone high up in New York in cancer.” The IRS agent replied [1].

Parallels with plant cancer

By 1925 Mayo’s Charles Mayo became interested in Erwin Smith’s discovery of cancer in plants, called crown gall. Livingston and Jackson, sensing a possible link between Smith’s work and their own, went to the Bronx Botanical Garden to request cultures of Bacterium tumefaciens, the plant cancer germ he had discovered. No mere accident led Virginia Livingston towards Smith’s work.

Smith stained his plant cancer germ with Fuchsin, long used to spot tuberculosis. And Smith’s bacteria, like Livingston’s, had many shapes. He had stumbled across B. tumefaciens in 1904, when he received some New Jersey daisies with overgrowths superficially resembling olive tuberculosis, a known disease of plants, but which proved to be plant cancer.

Smith had long suspected a bacterial cause for human cancer and criticized pathologists for drawing:

“Too sharp a demarcation between malignant tumors, on the one hand, where the cells of the animal or human host, acting under some unknown stimulus are responsible for the tumerous growth and granulomata (benign tumors) on the other hand, such as tuberculosis and actinomycosis, where a visible microbe is responsible for the primary tumor, and the direct migration of this microbe for any secondary tumors that may appear.” -Rogers, 1952

Smith’s conclusion:

“At the bottom, I think the distinction between such a disease, for example as tuberculosis or leprosy and malignant tumors is not as sharp as some histologists have been inclined to believe”. -Rogers, 1952

It could be said that at one time the entire medical and scientific community was set on fire by Erwin Frink Smith’s discovery of the bacteria that caused plant cancer. Twice honorably mentioned in The Journal of the American Medical Association, their Editorial “Is Cancer of Infectious Nature?” mentions how Smith’s work made “a very strong case in favor of his view of the infectious cause of cancer in general.” (JAMA, 1912)

By 1921, Margaret Lewis, of the Livingston Network, approached Frink Smith regarding her planned chicken inoculations with B. tumefaciens. Lewis would go on to elicit the cancer sarcoma from chick embryos using B. tumefaciens.

On January 31, 1925, an English abstract in the authoritative German Kinische Wochenschrift, written by Ferdinand Blumenthal, trapped Smith’s attention. Blumenthal, with assistants Meyer and Auler had shown that human cancer bore a microorganism closely resembling tumefaciens which in turn caused malignant tumors in plants as well as animals, complete with spread or metastasis.

Paula Meyer had worked with Friedlander on the human cancer germ since 1923. Her particular discovery was of a bacteria inside breast cancer which she called PM for Paula Meyers. She had also discovered closely related strains from 15 other human cancers. Smith examined stained slides of Meyer’s cancer germ from human breasts. It looked much like B. tumefaciens. Meyer’s germs were short rods, single or paired, and they stained with the same Fuchsin that he had used [22].

Moreover, when Blumenthal and Meyer inoculated their human cancer germ PM into plants, the tumors looked exactly like crown gall. That PM could produce plant cancer was now for Erwin Frink Smith beyond a shadow of a doubt. But it could not be B. tumefaciens itself, because no strains that he had tested grew at body temperature in warmblooded animals. His conclusion: that human cancer was probably due to some other microbe, possibly a mycobacteria, that had similar chemical activities to B. tumefaciens.

Seibert rules out contaminants in the cancer germ

The only time that Dr. Florence Siebert, long part of established medicine, ran into resistance and suppression, was when she decided to have a closer look at Livingston’s cancer germ. One of America’s finest Ph.D. ¬ Biochemist’s, while still at Yale she resolved the mystery of the many fevers coming from distilled water for injection and thought to be caused by fever-producing ‘pyrogens’, quickly proving that these were in fact bacterial contaminants. Having solved the mystery of pyrogens, Siebert was asked by Dr. Esmond Long to stay on at the University of Chicago to develop the Tuberculin skin test. Long suggested a European trip to learn techniques practiced on the continent [23].

At the Pasteur Institute of Paris, Seibert exchanged ideas with Boquet, Calmete and Guerin: the three investigators who presented to the world its only recognized vaccine for tuberculosis, called BCG [23].

Seibert returned to the US and when Long left Chicago to head laboratory operations at the Henry Phipps Institute in Philadelphia, she accompanied him.

By 1903, Henry Phipps, wealthy partner of Andrew Carnegie, sought a charitable outlet for his wealth. He then joined Lawrence F. Flick, a doctor with a vision to open a center solely dedicated to the study, treatment and prevention of Tuberculosis.

Still working off grants from the National Tuberculosis Association, Seibert was asked at Phipps to continue her work for a skin test using Koch’s original Old Tuberculin (OT). Seibert refined and purified the protein in her TB skin test. She named it PPD-S, both because it was a purified protein derivative and was intended to serve as a standard (S) for the US Government, which it eventually became. Then, after 30 years in tuberculosis research, Seibert turned towards cancer. In 1948, Margaret Lewis of Philadelphia’s Wistar Institute asked Seibert to do a nucleic acid analysis on Wistar rat tumor extracts, which Seibert agreed.

Next, Irene Diller, who networked extensively with Livingston, asked Seibert to look at her slides of the cancer microbe. Seibert relates what she saw:

“I saw tiny, round, coccoid organisms, many of which were magenta in color. The slides had been stained with Ziehl-Neelsen reagent, which we regularly used to stain our tubercle bacilli red. When I learned that she had isolated them from a rat tumor and could do so regularly from tumors in general, as well as from blood of leukemic patients, I asked, “Could you find them in the rat sarcoma tumor I am studying?” -Seibert, 1968

Diller agreed to try. Lewis allowed Seibert to forward the tissue sections. The results came back. The same cancer germ appeared. Seibert immediately saw the implications:

“This looked terribly important to me, and I was thenceforth willing to do whatever I could to help in this promising field. We did help by studying the immunological relationship to our tubercle bacilli, as well as to the “atypical” bacteria closely related to our tubercle bacilli.” – Seibert, 1968

Seibert was even more impressed with how Diller, following the footsteps of Livingston and Jackson, proved, thru Koch’s postulates, that her germ was the cancer germ:

“It is based on her (Diller’s) work that I am willing to say I believe she has found the cause of cancer, which I think no one can refute, and this work should be welcomed and confirmed by other cancer researchers, and not be ignored, even in view of the great stir at present about viruses.” -Seibert, 1968

Florence Seibert joined Livingston’s crusade in earnest in the 1960s, turning her cancer organism over to Frank Dunbar, chief of laboratories at the Southwest Tuberculosis Hospital in Tampa. Dunbar’s conclusion: her multi-formed germ did not belong to his groups of known “atypical” mycobacteria, even though they did have some of the properties of the mycobacteria [23].

Experimental medicine for the masses

Eventually Virginia Livingston gained university affiliations in San Diego working out of the University of San Diego with Dr. Gerhard Wolter of nearby San Diego State. In 1970, Wolter and Livingston discovered actinomycin-like compounds produced by the cancer germ, one of which, Actinomycin D or Dactinomycin, depite its toxicity, was being used in cancer. Livingston was aghast that her own discovery was being used this way. She cautioned that not only did actinomycins arrest the maturation of cells and inhibit the immune response but that they also inhibited enzymes and decreased hormone levels, stimulating the body to increase its hormone production [1].

She was puzzled as to why anyone would want to use a devastating substance like Actinomycin D for the subsequent treatment of cancer. Yet it was being done. Even more disturbing was the way in which organized medicine was responding to the hormonal disruption in the body caused by her cancer germ.

By 1966, Charles Huggins of the University of Chicago went to Stockholm and received a Nobel Prize for determining the effects of sex hormones on cancer that had spread. Following this, the practice of castrating cancer victims came into vogue. Consequently, someone came to the conclusion that if castration helped initially, any recurrence would better be treated by cutting out the adrenal glands, housed on top of each kidney.

And since this never produced earth-shaking results, a new procedure was devised to cut through the nose and remove the pituitary-the master gland of the body, lodged near the brain. Virginia Livingston had established that abnormal hormonal stimulation was coming from the toxic materials and hormonal derangers manufactured by her germ. In response America was chopping out the glands of its cancer patients.

White Knight

In The Cancer Microbe, Alan Cantwell acknowledged the invaluable help of four women who pioneered the early microbiology of cancer: Virginia Livingston, M.D.; Eleanor Alexander-Jackson, PhD; Florence Siebert PhD and Dr. Irene Diller [24].

Cantwell grew up reading that all germs responsible for the important diseases were supposed to have been already discovered. But much to his dismay, once a physician-researcher, he encountered the one left out: Livingston’s cancer germ. And although he knew that the many-shaped germ had long been considered a mere contaminant or secondary invader or even non-existent, Cantwell, like Seibert, knew better.

Cantwell first contacted Virginia Livingston thru the suggestion of a colleague who had heard her on radio and immediately sensed their common ground, which was, by then, the acid-fast bacteria found in Scleroderma and cancer. Despite her meticulous research, Cantwell knew that Livingstone had already been branded by traditional medicine as a charlatan, leaving what he thought to be perhaps the major discovery of the 20th century largely discredited [24].

By 1971, Cantwell had published on Scleroderma in the highly respected Archives of Dermatology and had no further intention of pursuing Livingston’s germ. Livingston, Jackson, Diller and Seibert had each drawn considerable fire from the medical establishment and despite Livingston’s persistent overtures towards him, there was no way he wanted in.

By 1974, Lida Mattman’s Cell Wall Deficient Forms [25], reconfirmed for Cantwell as well as others that many bacteria, but especially tuberculosis and the mycobacteria existed naturally in many forms a cycle of growth which involved “cell-wall-deficient forms” ranging from viral look-a-likes to bacterial forms to granules and then on to larger globoid shapes. But most physicians and laboratory scientists were being taught little about cell-wall deficient bacteria.

Cantwell’s silence threshold was exceeded forever when he again saw the cancer germ in the skin of the chest wall of a young woman who had lost both her breasts to metastatic cancer. Removing this patients skin lumps, Cantwell and colleague Dan Kelso at first cultured Staph. epidermiditis, a common contaminant. But as their cultures aged, the seeming Staph cocci became large globoids, rods and yeast-like forms with acid-fast TB-like granules everywhere [25].

Tracking down specimens of the woman’s original cancer, removed a year earlier, Cantwell not only isolated the variable acid-fast cancer germ in the tumor itself, but in surrounding specimens taken from the woman and thought by pathologists to be normal. This in effect established that the germ existed in the victims tissues before it became cancerous.

In a series of peer-reviewed, penetrating articles, Cantwell found the cancer microbe in three other cancers: Hodgkin’s, Kaposi’s cancer of the skin and a rarer skin cancer called mycosis fungoides.

It became obvious to Dr. Alan Cantwell after twenty years of microbe hunting that the old tenets of microbiology were not much use when it came to showing an infectious cause of cancer. In man as well as in nature, bacteria were constantly changing forms and evolving in their lifetime. The cancer microbe, unstable by nature, was no exception [25].

But 25 years after removing the metastatic breast nodules from the skin of a young mother and finding them variably acid-fast, there remained no cure for a germ which though tuberculosis-like, seemed indestructible. And a germ without a cure, as shown by the mixed reception to Koch’s discovery of tuberculosis, even decades later, fostered it’s own resentment and disbelief, a resentment and disbelief which Virginia Livingston never stopped facing.

BCG

It seems to me that it is entirely rational to state that the reason the BCG vaccine is effective not only against tuberculosis, but leprosy as well as cancer is because of the fact that the cancer germ is closely related to the BCG since it is in the same family, the Actinomycetales.

-Livingston, 1972

When Florence Seibert met Boquet, Calmete and Guerin in Paris to discuss their BCG, the only recognized vaccine for tuberculosis in the world, made from cow or bovine tuberculosis, none of them had any idea that it would one day be used against cancer. But in fact, currently, this diluted vaccination of Mycobacterium bovis or cow tuberculosis is the most effective treatment for transitional cell carcinoma, a cancer of the urinary bladder. Moreover, BCG is the most successful therapy of its kind, called ‘immunotherapy’ [26]. Within ‘immunotherapy’, it soon became fashionable to suppose that BCG or cow tuberculosis somehow ‘bolstered’ the immune system, but noted immunologist Steven Rosenberg held that the immune system was highly specific. One immune stimulant such as BCG should not stimulate a response from another immune stimulant, cancer [27].

The precise mechanism as seen by a 1993 University of Illinois study was that initially cancer cells seemed to eat (or phagocytize) and kill the Mycobacteria bovis in BCG. But then, suddenly, the cancer cells too died. Although investigators in the study admitted the relationship wasn’t clear, a strong ‘tumoricidal agent’, inside the Mycobacteria was pointed to [28]. Livingston felt that investigators were probably unwittingly looking at was a common phenomena in nature known as ‘lysogeny’. Lysogeny is what happens when one colony of a similar bacteria kills another by hurling viral phage weaponry towards it, without itself being harmed.

By the late 1970s Virginia Livingston could no longer ignore Chisato Maruyama of Japan and sent John Majnarich of Seattle’s BioMed Laboratories to Japan to have a closer look. In 1935, Maruyama, of the Nippon Medical School began to develop a vaccination against tuberculosis which turned out to be good against cancer. The Maruyama vaccine was similar to BCG, but instead of using cow tuberculosis as its base, the Japanese version used human tuberculosis.

Chisato Maruyama had long noted that patients with either the Mycobacteria tuberculosis or leprosy seldom had cancer [33]. By the 1970s Maruyama’s vaccine was proving quite successful in that he claimed that half of the 8000 cancer patients he had treated had benefited [29].

Livingston’s legacy

By the early 1970s Virginia Livingston, badly beaten by the medical establishment, was ready to launch a counterattack in the form of a fascinating study which showed that her cancer microbe secreted humanchoriogonadotropic hormone (HCG) a growth hormone long associated with cancer. Initially, despite laboratory evidence to the contrary, her contention that a bacteria could produce a human hormone was not believed. But then reports from traditional bastions such as Allegheny General, Princeton and Rockefeller University confirmed her findings.

Livingston believed that this growth hormone, secreted by her cancer germ built up uncontrollably to stimulate tumor growth, turning normal cells into malignant ones when either the body’s immune system was weak or essential nutrients were deficient. Dr. Hernan Acevedo of Allegheny, in fact, showed that all cancer cells had the hormone [30].

Livingston’s discovery, a medical milestone, gave further impetus to a microbial theory of cancer with well over a century of research behind it. Yet despite this, the premise behind an infectious cause was stubbornly refused by orthodox medicine.

Virginia Livingston was past 80 when she died on June 30th, 1990. Just months before, a subpoena was issued to her prohibiting her vaccinations, made from the patient’s own cancer germ (autogenous), with which she had had great success.

Following this, her vaccine was stigmatized as an “unproven method” in the March April 1990 issue of CA The Journal of the American Cancer Society[31] with references to her mistaking several different type of bacteria, rare and common for a unique microbe. This despite droves of research papers establishing mycobacteria as either coming before or coexisting with cancer. Ironically, Acevedo, who could not stop lauded her discovery that the cancer germ could manufacture human growth hormone was instrumental and key to the society’s damaging conclusion.

Yet when questioned by this author approximately a decade later, Acevedo admitted that he had ignored acid-fast forms which were indeed present in the cancer preparations Livingston sent to him. He felt these irrelevant, and mentioned that besides, the technology was not available at the time to pursue these acid-fast forms further.

On such fuzzy logic, it seemed that perhaps the most important scientific cancer lead in this or any other century was buried.

Conclusion

The striking analogy between cancer and tuberculosis was noticed long before the tubercle bacillus was discovered. In 1877, Sir John Simon clearly pointed out this analogy and in fact argued very strongly in favor of a microbial origin of cancer. But by 1910, certain American medical powers did an 180 degree rotation, deciding that cancer was not caused by a microbe and that anyone who thought otherwise was a heretic, a charlatan or a quack.

But Virginia Livingston was none of these. Rather she was a symbol of painstaking research and dedication at the height of post World War II American medical technology. Opponents of Livingston said that she saw “contaminants” of a group of commonly encountered germs. But Florence Siebert, an expert on contaminants who standardized the present day tuberculin skin test for the US government, saw no contaminants present and Dean Burk, then Head of Cell Chemistry at the NCI went so far to say that Livingston’s cancer germ was as real and certain as anything known about cancer [29].

Yet in the subsequent suppression of Livingston and her many colleagues by the medical establishment a picture emerges, and it is not a very pleasant one.

Virginia Livingston gained international status when she discovered that her cancer germ produced human growth hormone, long associated with malignancy.

However, at first even this was not believed. Had she gained the same stature regarding identifying the cancer germ itself, by today there probably would be no cancer. At this time there is admittedly no cure for Livingston’s cancer germ. Suppression led to its own disinterest in cure and each year a multitude must suffer and die as a result.

References

[1] Livingston, Virginia Wuerthele-Caspe, Cancer: a new breakthrough, Los Angeles: Nash Publishing; 1972.

[2] Ewing J. Neoplastic diseases. 2nd ed. Philadelphia: W.B. Saunders; 1919.

[3] Hunter D. The diseases of occupation. 6th ed. Boston: Little Brown and Company; 1978.

[4] L’Esperance E. Studies in Hodgkin’s disease. Annal Surg 1931;93:162 8.

[5] Livingston V, Allen RM. Presence of consistently recurring invasive mycobacterial forms in tumor cells. Microscop Soc Bull 1948;2:5 18.

[6] Sweany HC. Mutation forms of the tubercle bacillus. JAMA 1928;87:1206 11.

[7] Beinhauer LG, Mellon RR. Pathogenesis of noncaseating epitheloid tuberculosis of hypoderm and lymph glands. Arch Dermatol Syph 1938;37:451 60.

[8] Mellon RR, Fisher LW. New studies on the filterability of pure cultures of the tubercle group of microorganisms. J Infect Dis 1932;51:117 28.

[9] Livingston V, Alexander-Jackson EA. Cultural properties and pathogenicity of certain microorganisms observed from various proliferative and neoplastic diseases (published under Virginia Wuerthele-Caspe). Am J Med Sci 1950;220: 636 48.

[10] Boesch M. The long search for the truth about cancer. New York: GP Putnam’s Sons; 1960.

[11] Glover T, Scott M. A study of the rous chicken sarcoma No 1. Can Lancet Practioner 1926;66(2):49 62.

[12] Goodman LS, Gilman A. The pharmacologic basis of therapeurtics. 5th ed. New York: MacMillan; 1975.

[13] Skirvin JA, Relias V, Koeller J. Long term sequelae of cancer chemotherapy. Highlights Oncol Practice 1996;14(2): 26 34.

[14] Pukkala E, Kyyronen P. Tamoxifen and toremifene treatment of breast cancer and risk of subsequent endometrial cancer: a population-based case-control study. Int J Cancer 2002;100(3):337 41.

[15] Mankiewicz E. Bacteriophares that lyse Mycobacteria and Corynebacteria and show cytopathogenic effect on tissue cultures of renal cells of Cercopithecus aethiops. Can Med Assn J 1965;92:31 3.

[16] Dubos R. The white plague: tuberculosis. New Brunswick, NJ: Man & Society Rutgers University Press; 1987.

[17] Aaronson JD. Spontaneous tuberculosis in salt water fish. J Infect Dis 1926;39:315.

[18] Wuerthele-Caspe VE, Alexander-Jackson E, Smith LW. Some aspects of the microbiology of cancer, J Am Woman’s Med Assoc 8:7.

[19] Alexander-Jackson EA. A specific type of microorganism isolated from animal and human cancer. Bacteriol Org Growth 1954;18:37 51.

[20] Inoue S, Singer M. Experiments on a spontaneously originated visceral tumor in the Newt, Triturus pyrrhogaster. Annal NY Acad Sci 1970;174:729 64.

[21] Lwoff, A. Biologic order (Karl Taylor compton lectures), Cambridge, MA: The MIT Press; 1962.

[22] Rogers III AD. Erwin Frink Smith: a story of North American plant pathology. Philadelphia: American Philosophical Society; 1952.

[23] Seibert FB. Pebbles on the Hill of a Scientist, in: Florence B.

Seibert, author/publisher, St. Petersberg, FL 1968.

[24] Cantwell Jr A. The cancer microbe. Aries Rising Press; 1990.

[25] Mattman LH. Cell wall deficient forms stealth pathogens.

2nd ed. Boca Raton, FL: CRC Press; 1993.

[26] Schneider B. Specific binding of Bacillus Calmette Guerin

in urothelial tumor cells. In vitro World J Urol 1994;

1216:337 44.

[27] Rosenberg SA, Barry JM. The transformed cell/unlocking

the mysteries of cancer. New York: GP Putnam’s Sons;

1992.

[28] Devados PO, Klegerman ME. Phagocytosis of Mycobacterium

bovis BCG organisms by murine S180 sarcoma cells.

Cytobios 1993;74(296):49 58.

[29] Martin W. Medical heroes and heretics. Old Greenwich, CT:

The Devin Adair Company; 1977.

[30] Acevedo H. Human choriogonadotropin like material in

bacteria of different species: electron microscopy and

immunocytochemical studies with monoclonal and polyclonal

antibodies. J Gen Microbiol 1987;133:783 91.

[31] Congress of the United States Office of Technology Assesment.

Unconventional Cancer Treatments US Govt Printing

Office, Washington, D.C; 1990.

[32] Klieneberger-Nobel E. Origin, development and significance

of L-forms in bacterial cultures. J Gen Microbiol 1949;3:

434 42.

[33] Moss RW. Cancer therapy. the independent consumer’s

guide to non-toxic treatment and prevention. New York:

Equinox Press; 1997.

[34] Rusch HP. The beginnings of cancer research centers in the

United States. J National Cancer Inst 1985;74(2):391 403.

[35] Fraenkel E, Much H. Uber die Hrodgkinsche Krankheit

(Lymphomatosis granulomatosa), insbesondere deren Atiologie.

Z Hyg 1910;67:159 200.

End of article

As you can see this is very good evidence that cancer is germ related and can thus be cured so why isn’t anyone stopping all this bullshit “Help stop Cancer Campaign” to reap in billions of dollars for the pharmaceutical industry and cancer charities etc?

What about how the US planted HIV/AIDS into the World

More Evidence HIV Was Made At Ft. Detrick

From Alan Cantwell MD

6-2-7

I am a physician and AIDS researcher who has authored two books on the man-made origin of HIV/AIDS (“AIDS & THE DOCTORS OF DEATH: AN INQUIRY INTO THE ORIGIN OF THE AIDS EPIDEMIC” and “QUEER BLOOD: THE SECRET AIDS GENOCIDE PLOT.”).

On the eve of the Blue Moon of May 31, 2007, I was sent the most explosive email I have ever received concerning possible insider evidence pertaining to the man-made epidemic of AIDS. The communication was sent by Sue Arrigo, M.D., who claimed she was a physician licensed in California (G50197). Because her email (attached below) was so mind-blowing, I immediately googled Arrigo and found several entries including a note on one website in which Arrigo claimed to have been kidnapped, raped and threatened with death in 2004 (this was NOT mentioned in her email to me). In addition, I checked online and verified that she was indeed a licensed CA physician, although her license expired in December, 2006, and her current residence is in Canada.

In her email Dr. Arrigo asked if I would help her get the word out to interested persons. I would ask that anyone who receives this communication to do all they can to spread the word regarding her accusations that AIDS is a man-made disease.

Over the past two decades there have been only a handful of other physicians and health professionals who have had the courage to alert the public to evidence that AIDS is man-made (namely Robert Strecker MD, William Campbell Douglass MD, Eva Snead MD, and Leonard G Horowitz DDS) . In general, their research (books, videos, internet communications) have been ignored by the CDC, the NIH, the AIDS establishment, the major media, etc. — and merely passed over as “conspiracy theory” and “paranoia.” Dr. Arrigo has a long association with the CIA as an expert on biological warfare, and also has apparent ties to the highest powers (and presidents) in the U.S. government. Thus, her insider status makes her an extremely valuable witness to the truth about AIDS and its man-made origin.

Please do all you can to confirm or deny the truth of Dr. Arrigo’s accusations — and to publicize her plight — and to air her plea on behalf of the abominations of secret biological warfare experimentation and use against human beings.

I have attached the google references to “sue arrigo”, her email to me in it’s entirety, proof of her CA medical credentials, and a website note of her rape and torture.

In truth and justice,

Alan Cantwell M.D.

alancantwell@sbcglobal.net

On May 31, 2007, at 8:32 PM, Sue Arrigo wrote:

Dear Dr. Cantwell,

Thank you for your courage and integrity in speaking the truth.

As an ex- CIA physician with high level access, I wrote a report for DCI Webster in about 1991 arguing for closure of all the US Bio-Warfare Labs. I did that after reviewing the Ft. Detrick and the CIA’s Langley Bio-Warfare Labs’s research, looking at their own documents. That review was authorized because Bush, Sr. had sold dangerous Bio-Warfare agents to Hussein, which I ended up having to recover from Iraq. Webster, as a former judge, willing to evaluate the evidence, allowed me to research the field and write a report for him of close to 100 pages and 1000 pages of supporting documents.

Although the focus of my report was why the Bio-Warfare Labs should be closed, the issue of the HIV virus developed by the Ft. Detrick lab formed about 18 pages of my report. At the time I wrote that report, the vaccine for HIV that had been developed in 6 months of work, had already been used by the Cabal since 1983.

It was a crime against humanity that the virus was unleashed on the world, and it continues to be a crime that the vaccine has been kept secret and for private use only. Meanwhile, the outer research to get to a vaccine is an exercise in how not to arrive at a solution before millions more die. The initial “hopes” for HIV per its designers was to be able to walk into Africa and take the resources from a ghost continent. They had hyped it as killing everyone there within a year, in their pre-release reports.

The research at the Labs addressed the fastest way to make vaccines to Bio-warfare agents, both in labs, at a front, and impromptu on a battlefield. That was a pressing concern and one that was researched using millions and millions of dollars.

Briefly, the consensus at the time was that

1) Any agent from a sick soldier left in a Waring Blender for 8 hours would be broken down well enough to not be infective in small doses ( ie. less than a 100 germs). The Labs had made an IgM set of antibodies to sediment out the human HLA antigens by centrifuging it. That allowed the supernatant to be used as a vaccine with little serum sickness problems. A physician in a war zone equipped with a Waring Blender, a blood specimen centrifuge, and a vial of the IgM could make a fast “fresh” vaccine and start inoculating soldiers. The labs tested that using a variety of agents and common cold agents. It was only if one wanted to store the vaccine in vials that one got into the problem of denaturing the proteins of the agent due to heat, chemicals,etc. That was where most of the problems of loss of effectiveness crop up.

2) The Labs found that causing a 1cm by 1cm abrasion until one got lymph and applying a drop of the “fresh vaccine” and a band aid, worked almost as well as an injection. The abrasion could be caused by three fast firm strokes of very fine sand paper over a template with a square of skin bulging through it. This method had much less serum sickness problem. The major problem was occasion keloid and scar formation and superficial infections.

3) The Labs also showed that it was possible to make a crude live vaccine as an emergency directly on the battlefield. The principle was that infection occurs when the body’s defenses are overwhelmed but that the body can usually fend off 10 to 50 organisms even of Bio-warfare agents. It was a simple dilution to get the agent into the right ballpark, starting with a secretion of a sick person. Then a drop of that dilute live agent would be placed on an abrasion. That was also tested during war games with colds etc. The diluted material can’t be stored for longer than an hour due to the risk of multiplying the agent. It was assumed that in the field it would not be known whether the agent was a virus or a bacteria. A bacteria that divided every 20 minutes could be 8 fold in quantity after an hour and risk causing the infection one was attempting to prevent. Of course, such a live agent could be extremely dangerous and except in an extreme emergency would not be used.

4) The issue of how to quickly sterilize a make-shift vaccine was also addressed in the research. The best method was to dry the agent, if time permitted. Second best was to preserve the agent in Vodka (40%), not gin, etc., and then to dilute it down to less than 2% alcohol before applying it to the abrasion.

That means that a simple vaccine for HIV can be made by virtually anyone in the world in a short period of time, though it would likely need to be repeated periodically to get and keep the titers up. But repeating it is a good idea anyway as that helps address the mutation problem. So, suppose one took 1 cc of secretions from each of 10 HIV patients in an area (without fungal infections preferably) and mixed them together to have a range of HIV agents. Then one could add 250 cc of Vodka and let it sit a week. Then one could remove a cc of that and add 20 cc of clean water to get a less than 2% alcohol solution. A drop of that could be applied to an abrasion. That, I believe, would give you about 60% protection. Repeating that at intervals of about 2 weeks to a month for 6 months and using new HIV secretions every 6 to 12 months, I think would give one fairly good protection in a person with a normal immune system to start with. Of course, that is a crude method and should be tested for efficacy etc. But it is simple enough to test on sex workers, if they were willing to volunteer. They are at such high risk that the likely benefits almost certainly outweigh the risks. The chief risk would still be sensitization with human HLA proteins. The beauty of using abrasions is that one can wash the vaccine off as soon as any untoward reaction is noticed.

If you know of people doing HIV research who are not controlled by the US govt, could you please pass this information on to them?

It would be good to get it out to those who could investigate this information with the intention of saving lives with it. Bio- warfare research is immoral and illegal. Unfortunately the US govt is accelerating that research and production of secret private vaccines.

Sincerely, Sue Arrigo, MD

(the below is from: http://www.alternet.org/rights/27771/)

An American Already Tortured By Cheney’s Team in the US

Posted by: kunzangwangmo on Nov 11, 2005 10:16 PM

As a coerced CIA asset, I was asked by Cheney in Aug. 2004 to frame Iran as developing nuclear weapons. Because Cheney was afraid of CIA leaks, he gave me the assignment at a Chinese restaurant in DC after hours. It was not the first meeting that I have ever had privately with him as I acted as a negotiator between him and Tenet. Within the CIA I had been an outspoken critic of US wars of aggression, its nuclear first strike plans, and its breaking of nuclear arms control treaties. I spent most of my life as an operative risking my life as a remote viewing spy monitoring and recovering lost WMD.

I am a doctor and the assignment Cheney gave me was to go to Iran as a physician. Once in Iran, a camera crew would be filming when an Iranian agent would rush in to say that he knew a secret bunker where the Iranian govt. was developing nuclear weapons. Cheney admitted that the rest of the filming would occur in Hollywood with a mock up of said lab. Clearly, this was an immoral assignment. There was no way that I was going to have the blood of innocent Iranian women and children on my hands, so I refused. When I did so, Cheney threatened the life of my mother. Since my mother had recently told me she would rather die than have me be emotionally blackmailed in this way, I held to my no.

During the course of our about 40 minute talk, one of his secret service officers interrupted us twice. The next week when I was kidnapped in Virginia, raped and tortured for 4 days, I recognized the voice of that officer as one of the rapists.

It is an outrage that Cheney is advocating torture. He has already shown by his actions, that he will stop at nothing, not even the torture of American born CIA personnel in order to get his way. He has a clear conflict of interest in making money off these wars. Are we, as Americans, going to torture people just so that corrupt officials can line their pockets with oil and war profiteering revenues?

Please write your congresspersons to prevent others being tortured as I was. Cheney and Bush should be impeached for lying to force us into war. We are not winning the war on terrorism, torture is terrorism as anyone who had been through it knows. I was raped and subjected to three mock executions, when will this US reign of terror end?

Sincerely,

Sue Arrigo, MD

California medical license G 50197

Every Church A Peace Church Speakers Bureau

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Subject: Sue Ann Arrigo, MD/ CA medical license information verification

Physician Information

Licensee Name:

SUE ANN ARRIGO, MD

License Type:

PHYSICIAN AND SURGEON

License Number:

G50197

License Status:

LICENSE DELINQUENT

Public Record Actions:

NONE AVAILABLE ON WEB SITE (To find out what information is and is not available on the Web site, please click here.)

Original Issue Date:

JUNE 27, 1983

Expiration Date:

DECEMBER 31, 2006

Address:

(withheld by Dr. Cantwell for privacy reasons)

Country:

CANADA

Public Disclosure

To find out what information is and is not available, please click here.

If information is posted in the Administrative Disciplinary Actions or Administrative Citation Issued categories below, documents may be available for review. Please click here to search the public document database.

Administrative Disciplinary Actions

No information available from this agency

Disciplinary Actions Taken by Other State or Federal Government

No information available from this agency

Felony Convictions

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Misdemeanor Conviction

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Administrative Citation Issued

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Hospital Disciplinary Actions

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Malpractice Judgment

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Arbitration Award

No information available from this agency

Education

Medical School:

UNIVERSITY OF CALIFORNIA IRVINE COLLEGE OF MEDICINE

Year Graduated:

1976

This information is updated Monday through Friday - Last updated: MAY-31-2007

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Dr. Alan Cantwell is a retired dermatologist; and the author of

five books on the man-made origin of AIDS and the infectious origin of cancer, all published by Aries Rising Press, PO Box 29532, Los Angeles, CA 90029 (www.ariesrisingpress.com). Email:alancantwell@sbcglobal.net. Abstracts of 30 published papers can be found at the PubMed website. Many of his personal writings can be found on http://www.google.com by typing in key words "alan cantwell" + articles. His latest book is Four Women Against Cancer: Bacteria, Cancer and the Origin of Life. His books are available on http://www.amazon.com and through Book Clearing House @ 1-800-431-1579]

Alan Cantwell M.D.

alancantwell@sbcglobal.net

http://www.ariesrisingpress.com

FOUR WOMEN AGAINST CANCER:

Bacteria, Cancer and the Origin of Life

MMR Vaccines and connection to autism

Whistle blower drops a bombshell in the United States

Vaccine-autism connection: US Congressman stonewalled by CDC, by Jon Rappoport, August 21, 2014

Posted on August 21, 2014 by Jean

http://www.nomorefakenews.com

With a CDC whistleblower standing in the shadows, claiming the CDC has known about the vaccine-autism connection for 10 years, the cover-up is threatening to blow sky-high.

And now Florida Congressman Bill Posey has sent me a statement about his experience with the CDC.

Posey has been trying to obtain specific data about a 2004 CDC study which claimed the MMR (measles, mumps, rubella) vaccine has no role in causing autism.

The CDC whistleblower (so far, anonymously) has been pointing to that 2004 study as a fraud, claiming vital data were omitted, data which would indict the vaccine.

So how has the CDC responded to Posey’s inquiry and request for all the 2004 data?

Here is what he wrote to me:

“The CDC has refused for more than six months to hand over documents I requested concerning this issue. That is not the type of response we expect from our government.”

What??

A US Congressman wants research data from a federal agency and they flat-out refuse.

Nothing much is a stake here—only the health of the entire US population. Vaccines causing autism? And the CDC has the right to keep as many secrets as it wants to?

Did the CDC wake up one morning and decide it’s the CIA? On what grounds is it refusing to release the data? National Security?

Here is what the CDC whistleblower (a research scientist still employed by the CDC) states: intentionally omitted data from the 2004 study shows that: African-American boys who receive their first MMR vaccine before the age of 36 months have a 300% increased risk of developing autism.

Presumably, this is what Congressman Posey would learn if the CDC turned over the data to him.

And who knows what else he would learn?

My comment about the CDC thinking it’s the CIA isn’t entirely facetious. In 1987, I confirmed that, routinely, certain CDC employees are sent to Langley, Virginia, for CIA training, and return with top-secret classifications—meaning they can access data that are off-limits to the rest of the CDC and most of the federal government.

Data confirming extensive and ongoing damage caused by vaccines might indeed rate as “classified, National Security,” if by Security you mean “protecting vaccine manufacturers and their government allies.”

As opposed to protecting the public.

Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free emails at NoMoreFakeNews.com.

End of article

I myself have exposed the HPV scam regarding the mass vacination of almost every highschool girl and now boy (Worldwide) whilst in their teens. This HPV vaccine is not only unproven but also higly unsafe with no proven data and in actual fact has actually killed more children that the very disease it is supposed to prevent…..it must also be noted that this same vaccine may lead to gross infirtility… which if true helps the United Nations/WHO acheive their own “Agenda 21 Mass Depopulation Plan.”

You decide.

Peter Eyre – 25/8/2014

Middle East Consultant – Political Analyst – Investigative Journalist – BroadcasterLivingston: