Is there a cure for cancer? You bet there is! Part 5

 

Dr. Virginia Livingston who found a cure for cancer

As we near the end of the current series on the cancer scam I want to introduce you to other experts that have either worked with Dr. Virginia Livingston or who believes in her invention/protocol.

One of the first that comes to mind is her dear associate and friend Dr. Alan Cantwell who can be seen with Dr. Livingston in the above photograph.

His expertise is second to non and in this part it would be appropriate to print a full interview carried out with Dr. Cantwell back in 2007 who also happens to give reference to many other fine cancer researcher, most of whom were never identified or given the chance to prove they had all found a combined cure for cancer and many other bacterium based diseases:

11 Sep 2007

Dr. Alan Cantwell has investigated the phenomenon of cancer bacteria for over thirty years. A graduate of New York Medical College, Cantwell completed a residency program in dermatology at Long Beach Veteran’s Administration Hospital in Long Beach, CA and then practiced in the dermatology department of Kaiser-Permanente in Hollywood, California, from 1965 until his retirement in 1994. Dr. Cantwell is the author of more than thirty published papers on breast cancer, lymphoma, Kaposi’s sarcoma, Hodgkin’s Disease, lupus, scleroderma, AIDS, and other immunological diseases. These papers have appeared in many peer-reviewed journals, including Growth, International Journal of Dermatology, Journal of Dermatologic Surgery and Oncology, and the Archives of Dermatology. He has also written The Cancer Microbe and Four Women Against Cancer and several books on AIDS.

Dr. Alan Cantwell

 

1. How did you become interested in looking for bacteria, first in diseases like scleroderma and later in cancer?

It all started when I was a second year resident in dermatology. I was in the medical library and I came across a paper in the Southern Medical Journal describing a group of people who had been given allergy injections and who subsequently developed deep skin infection with tuberculosis-like germs. It was thought the allergy injection bottles were contaminated with these bacteria.

At the time, I had a mentally disturbed patient who had been given multiple injections of medications into her buttocks. She later developed deep painful skin nodules in the same areas. No one knew what was causing these nodules that were diagnosed as “panniculitis,” an inflammation of the fat layers of the skin. I thought, “Let’s culture a skin biopsy from one of these deep nodules and see if I can find any TB-like germs.” I was amazed when Eugenia Craggs, the technician at the TB lab, reported that “acid-fast” bacteria were discovered in the skin tissue. I thought “Hey this is just like the article!”

We also had three other patients with “panniculitis” of the fatty portion of the skin, all of unknown cause. I took biopsy samples and TB-like bacteria were found in all four. These cases were later reported in the Archives of Dermatologyin 1966. At the time my dermatology professor was J. Walter Wilson, who was also a world famous mycologist, an expert in fungal diseases. He was somewhat skeptical about my findings of acid-fast bacteria in all these four patients and he suggested I use a scleroderma patient as a “control.” Scleroderma is a so-called “collagen disease” where the skin becomes hardened. The disease can affect the internal organs and is sometimes fatal. The cause is unknown, and bacteria were never thought to cause this disease. Dr. Wilson said I should check a scleroderma skin biopsy because that would serve as a negative “control” case. I was astonished when Eugenia Craggs called me from the TB lab and told me the skin tissue grindings of the scleroderma sample were positive for acid-fast bacteria, the kind of bacteria found in tuberculosis. She would try and grow the germ in a TB culture. After much searching I was also able to find a few acid-fast rod forms of bacteria in the scleroderma skin biopsy microscopic sections prepared by the pathologist.

The scleroderma bacterial took a long time to grow and could not be diagnosed as a TB germ or other definite “atypical” mycobacteria. The microbe was highly pleomorphic (various forms). There were round staphylococccal forms, as well as typical acid-fast rod forms. Eventually this isolate became fungal-like and “actinomycete- like.” Despite expert opinion, it was impossible to classify the microbe into a specific species. This case of scleroderma was reported in The Archives of Dermatology in 1966.

Some time later, Roy Averill, one of the dermatology residents, told me he heard a woman physician being interviewed on a San Diego radio talk show. She was explaining how she found TB-like bacteria in scleroderma in the late 1940s. That woman was Virginia Livingston M.D. She quickly became a dear friend and mentor in my scleroderma research. She told me that scientists at the Pasteur Institute in Belgium also reported finding acid-fast bacteria in scleroderma in 1953, thus confirming her own research.

I naturally thought all these reports in the medical journals would be recognized by other dermatologists and scientists, and that scleroderma would be recognized as an infectious disease caused by acid-fast bacteria. But after more than a half-century, I’m sad to say that scleroderma is still considered a disease “of unknown etiology” and the bacteria we found are simply ignored. After discovering acid-fast bacteria in scleroderma, Livingston found similar bacteria in cancer. This made her one of the most controversial physicians in America, as detailed in my book, “The Cancer Microbe.”

2. How did you identify the bacteria in your samples?

I began my dermatology practice at Kaiser in Hollywood in 1965. Virginia Livingston introduced me to Dan Kelso, a Los Angeles microbiologist who thereafter cultured my skin biopsy samples from scleroderma, and later from lupus erythematosus and a variety of cancers. Depending on the case, sometimes he cultured Staphylococcus epidermidis, or corynebacteria, more rarely streptococci, and pleomorphic bacteria that appeared sporadically as acid-fast bacteria similar to Mycobacterium tuberculosis.

Naturally I attempted to find acid-fast rod forms in my specially-stained skin biopsy sections, because these forms are the typical forms signifying infection with Mycobacterium tuberculosis or other species of mycobacteria. “Acid-fast” refers to red-stained mycobacteria that can be observed after staining tissue samples with a special procedure and a special dye. At first, I didn’t see the L-form bacteria since they react differently to acid staining. Instead of rod-forms, they appeared as round forms which were only partially acid-fast, staining purple or magenta with the acid-fast stain. It took me many years to finally realize that these partially acid-fast and round forms were bona fide growth forms of mycobacteria. The typical bright red-stained acid-fast rod forms of mycobacteria are unique and easily recognized by pathologists, but unfortunately the non-acid-fast round forms are not recognized and accepted by pathologists. For a long time I passed over these granular and “dusty” tiny forms as meaningless, not realizing that they were, in actuality, what L-forms look like!

I knew basically nothing about the microscopic appearance of L-form bacteria (also known as cell wall deficient bacteria and “mycoplasma”) until I carefully read the published papers of microbiologist Lida Mattman. Then I realized all the guises that bacteria can undergo, including transformation into “large bodies.” At that point, I went back and looked at my first case of scleroderma and realized that one skin biopsy sample contained large L-form bodies that appeared as yeast and fungal-like forms! These forms, in 1966, were dismissed as “fat degeneration” by one pathologist; and the biologist thought they looked like yeast cells.

These large L-forms are compatible with what pathologists recognize as Russell Bodies. William Russell (1852-1940) was a well-known Scottish pathologist who first discovered “the parasite of cancer” in 1890. His view of an infectious agent in cancer was dismissed in the early part of the twentieth century. However, I believe Russell bodies are actually large growth forms of cell wall deficient bacteria — and that Russell was indeed recognizing an infectious agent in cancer. More than a half-century later, Lida Mattman was able to transform mycobacteria into “large bodies” by exposing them to antibiotics. For more information on Russell and pictures of Russell bodies, Google my paper “The Russell Body” in the Journal of Independent Medical Research (joimr.org).

The fact that L-form bacteria have a “life cycle” and can appear in so many different shapes and sizes (pleomorphism) may be why they are so hard to eradicate and why the immune system cannot cope with them. Maybe the large Russell bodies are harder to kill. Or maybe they are easier to kill. I don’t know.

3. You found bacteria in the tissues of people who died of certain cancers and AIDS and scleroderma at autopsy. What gave you the idea to look for bacteria in autopsies?

I got that idea from Florence Seibert, a world famous biochemist who developed the tuberculin skin test for tuberculosis, which is still used worldwide. When Seibert heard about the TB-like bacteria discovered in cancer by Virginia Livingston and her colleagues, which included microbiologist Eleanor Alexander-Jackson and cell cytologist Irene Diller, she decided to come out of retirement and help with the women’s cancer research. Seibert advised me to search for bacteria in autopsy specimens and to determine if I could also find them in the internal organs and connective tissue of people who died of scleroderma. She believed this would make my skin research more credible. For the full story of these four remarkable women scientists, read my book Four Women Against Cancer, published in 2005, and available through Internet book sources.

Alan Cantwell with Eleanor Alexander-Jackson and Irene Corey Diller

After I decided to look for bacteria in autopsy material, I contacted colleagues in the Pathology department at Kaiser and asked them to provide me with stored tissue autopsy samples, which they did graciously. I was very fortunate to have them assist me in doing this. One of the great things about Kaiser-Permanente is that everything is under one roof. Few private dermatologists would have the easy access to autopsy material that I did at Kaiser.

4. When did you begin to look for bacteria in people with cancer?

Never in my wildest dreams did I think I would ever find bacteria in patients with cancer. Before I started my cancer research (which was totally instigated by my friendship with Livingston), it seemed inconceivable that scientists could have failed to recognize a microscopically visible infectious bacterial agent in cancer.

For a decade I avoided the cancer controversy because I worked for an HMO and I didn’t want to be regarded as a “quack.” Tragically, Virginia Livingston, because of her outspokenness that cancer was caused by bacteria, was widely regarded as a “quack doctor.” However, in the mid-1970s, I found pleomorphic bacteria in patients with sarcoidosis, and also in a patient with lymphoma. I was amazed at how easy it was to detect bacteria in sarcoidosis and lymphoma when the tissue sections were properly stained with an acid-fast staining technique.

Once I saw for myself that Virginia Livingston was correct about acid-fast bacteria in cancer, I became very enthusiastic about studying bacteria in other forms of cancer, as well as in immune diseases, like lupus. At that point, I finally had enough conviction in my findings, and had the courage to take a stand along with Virginia.

5. How did you colleagues react to your research?

Over the years there were very few doctors interested in seeing the bacteria I found in tissue sections. Some would tentatively acknowledge that there were bacteria present. Most were non-committal. With a little arm twisting I convinced several pathologists, who helped supply the autopsy specimens, to put their name on my published papers. But for the most part they didn’t want to get involved. They would say, “Oh Alan, it’s your research…” “Oh Alan, you’ll win the Nobel Prize someday.” Nobody ever wanted to sit down with me and seriously look at the material. I think it’s because finding bacteria in illnesses that are not attributed to infection is highly controversial, and most doctors shy away from controversy. The finding of bacteria in cancer is like opening Pandora’s Box. Once it’s open, a lot of stuff flies out, and pisses off a lot of people. The bacteria aren’t supposed to be there, they are in closet and not supposed to come out.

Even after I was retired for almost a decade, I never lost interest in trying to uncover bacteria in cancer. In 2003, my partner was diagnosed with prostate cancer. He underwent a prostatectomy, the total removal of the prostate gland. I decided to see if bacteria could be found in his prostate cancer tissue sections after surgery. Prostate cancer is every older man’s worst nightmare, just as breast cancer is every woman’s worst nightmare. I asked the Kaiser pathologist to cut me a section of my partner’s cancerous prostate and to stain it with an acid-fast stain so that I could study it. Sure enough, there were bacteria in the samples. I had a private microscopist photograph the bacteria. One can view the bacteria in prostate cancer I discovered by reading my paper published at the http://www.joimr.org website.

6. What’s going on? Why aren’t doctors and researchers taking the idea that bacteria cause cancer seriously?

As I see it, the identification of simple-to-see cancer microbes would cause havoc in the scientific world and in the cancer treatment industry. It would be the biggest embarrassment to befall modern medicine. Can you imagine the furor resurrecting Russell’s “cancer parasite” — the “parasite” that was thrown out of medical science a century ago?

It is rare to find a scientist interested in “cancer microbes.” Most physicians are repelled by the idea that bacteria cause cancer. How do you prod scientists to become interested? I’m still not sure.

A century ago, doctors stopped looking for bacteria in cancer. It’s weird because around that time major diseases like syphilis, tuberculosis, and leprosy were proved to be caused by bacteria. I suppose researchers think, “Well, we looked for bacteria 100 years ago, so there’s no need to look for them now.” But a lot has changed in bacteriology in 100 years. A century ago there was no such thing as an “L-form.” Even now most scientists don’t realize that regular bacteria can change into L-form bacteria, or cell wall bacteria, or mycoplasma, or pleomorphic bacteria, or nanobacteria, or whatever you choose to call these peculiar and little-known growth forms.

Microbiologists still have a hard time dealing with the fact that bacteria can change so widely in shape and size. How do you get scientists to understand that the tiniest L-forms have the potential to enlarge into a form the size of a red blood cell (or even bigger!). But if you think about it, all human beings were once a microscopic bunch of dividing cells, hardly visible to the naked eye. And we know that these tiny cells can evolve into seven foot tall basketball players. Why then, do we take such a simple view of what bacteria are supposed to do and what they are supposed to look like?

And the strange part is that using a light microscope you can easily see L-form bacteria. Every scientific paper that I have had published shows pictures of these bacteria. But even when doctors are shown photographs or see these bacteria via a light microscope, they still have a hard time accepting them. It’s bizarre because doctors believe viruses exist, even though most have never seen one. You can’t see viruses. They are too small to be seen with a microscope.

7. When doctors and researchers claim that there are no bacteria in your samples what explanations do they give?

When doctors or other researchers try to deny that there are bacteria in scleroderma and cancerous samples their explanations are pretty lame. Maybe something like, “Those aren’t bacteria, those are enlarged red blood cells.” Those “bacteria” are really cell debris, or stain material, or nuclear dust, of mast cell granules, or fat granules— anything but true bacteria. It’s impossible to convince a pathologist, for example, that a “tiny” bacteria can transform into a giant-sized form hundreds of times larger.

8. Who’s to blame for the fact that bacteria have not been recognized as part of the pathogenesis of cancer?

Pathologists, dermatologists, infectious disease specialists, oncologists, virologists, microbiologists, and basically all medical scientists who have ignored a century of cancer research pointing to cancer microbes. They have collectively let us down. Unfortunately, pathologists and microbiologists seem to be on two different planets. Pathologists pay little attention to germs in a laboratory, and microbiologists pay little attention to what bacteria do when they infect human tissues that are subsequently examined by pathologists.

9. What keeps other researchers from finding L-form bacteria in patients with cancer?

Unfortunately, most microbiologists who have worked with L-form bacteria have not demonstrated how these same forms appear in tissue in human disease when viewed in the light microscope. It’s one thing to describe a microbe in a lab, but what does it look like when it infects the human body? It’s one thing to show these L-forms in pictures taken with an electron microscope that magnifies objects thousands of times. But what do these bacteria look like when view with a “regular” light microscope that magnifies only 1,000 times? As a result, these pleomorphic forms go undetected in diseased tissue. Another reason, of course, is that the pathologist uses a routine stain (the H&E stain) that does not detect these forms. One needs to use an acid-fast stain. This was one of Livingston’s and Eleanor Alexander-Jackson’s most brilliant discovery— the idea that the “cancer microbe” is intermittently “acid-fast” at one or more stages of its growth.

10. What are some of your concerns about the current medical climate?

It saddens me greatly that all this great research has been ignored. That is why I wrote The Cancer Microbe (1990), and AIDS: The Mystery and the Solution(1984) and Four Women Against Cancer (2005).

Every first year med student knows that until you know what’s causing a disease it’s very hard to treat it. In my opinion, hunting for the exact cause of an illness is the most exciting part about being a doctor. The scientists who clued us into the cause of tuberculosis and syphilis, for example, were medical greats because they gave us an idea of what exactly is making the patient ill.

In my 30 years as a doctor and researcher I’ve never convinced one doctor, not even one, that bacteria cause cancer. My own younger brother is a physician — and I don’t even think he believes me entirely. Two years ago, his daughter-in-law died at age 39 of Hodgkin’s Disease, leaving two small children. I told him, “I wrote about Hodgkin’s Disease!” But he wouldn’t comment. If I can’t convince my own brother — or even interest him in the subject —I feel there is little hope.

11. What concerns did Kaiser Permanente have about your research?

A problem with my research was that over a period of years I was finding acid-fast bacteria in patients with a wide array of different illnesses. Some skeptics would say “OK, maybe I can accept that you found bacteria in scleroderma, but come on, in all these diseases?” After several years of productive cancer microbe research, the research committee insisted I be interviewed by a statistician. The committee was concerned because I was discovering bacteria in too many diseases. The statistician insisted that I attempt a statistical study of these bacteria with suitable “controls.” I explained that previous researchers had already determined that all human beings harbor such bacteria, and that these bacteria needed further study as pathogens. It might be impossible to find “negative” controls. At that point I thought, “I’m doomed.” There was no way I could do a statistical analysis of my observations. My research was terminated.

12. Did anyone try to censor your work?

In 1984 Virginia Livingston wrote a second book about bacteria in cancer calledThe Conquest of Cancer. She asked me to write a blurb for the back cover of her book. Her publisher took out an ad for her book in the Los Angeles Times Book Review, which included my blurb. Unfortunately, my quote mentioned my association with the Southern California Permanente Medical Group. When the top brass at Kaiser discovered this they were furious. “You can’t do this! You can’t associate our name with a quack like Livingston!”

At the time I had also discovered that cancer bacteria play a role in the development of Kaposi’s sarcoma, the most common cancer in the newly discovered disease called AIDS. I explained that I had also written a book about AIDS and the bacteria involved in this disease, and that the book was in press and was to be published soon. The Kaiser officials were aghast and told me I was simply not allowed to publish this book. This was at a time shortly before the discovery of HIV and during the period when the precise cause of the immune deficiency was “a mystery.” I had always been well-respected at Kaiser, but I was fearful the Livingston brouhaha and the impending publication of my book might threaten my job.

Finally my literary lawyer stepped in and worked out a deal with Kaiser whereby I could publish AIDS: The Mystery & The Solution as long as I didn’t mention Kaiser in the book. I had to make sure the printer deleted all references to where I had done my cancer and AIDS research. The thing I had tried to avoid for so long had become a reality: I had inadvertently become a threat to the medical establishment, just like Virginia Livingston.

13. Tell me about your role model and colleague Virginia Livingston.

Virginia was a dear friend whose research formed the foundation of my scleroderma research and subsequent cancer microbe studies. My association with her and Irene Diller and Eleanor Alexander-Jackson and Florence Seibert, changed my life forever. Although she died in 1990 at the age of 84, Virginia still influences me. She is my “scientific soulmate.” These four women are my four greatest heroines in medical science. In Four Women Against Cancer, I describe their amazing cancer research. I knew them all personally, and sadly all of them are now gone.

14. What do you think about the Marshall Protocol?

When I heard about the Marshall Protocol I was taken aback. I never thought that a possible cure for chronic disease would happen in my lifetime. I used to tell people that there was no way known to kill L-form bacteria in the body.

In mid-life Trevor Marshall set out to figure out a good treatment or a cure sarcoidosis because he had the disease himself. That is how — via his own research — that he discovered me and I was made aware of his own admittedly controversial ideas on how chronic diseases might be successfully treated. He certainly, almost single-handedly, revived my scientific career and I am exceedingly grateful to him for his interest and support of the cancer microbe work.

Having a disease is unfortunate, but it can serve as a great consciousness-raiser. Illness can also bring people together who would have never been brought together otherwise. This interview is a good example of that! From Trevor I am learning about the importance of the “vitamin D receptor” and that Benicar, along with long-term antibiotics can help rev up the immune system and apparently diminish L-form bacteria in patients who are trying his ideas. It’s interesting because Livingston always said that the key to curing chronic disease and cancer is to improve the function of the immune system. In my opinion, the proof is in the pudding. Some people with chronic disease are reporting benefit from the MP.

Trevor’s not a medical doctor but he obviously is an avid researcher and well-versed and well-trained in biochemistry, pharmacology, molecular biology, subjects that are way beyond my ken. Plus, I went to medical school a half century ago.

The MP has revealed that the healing process of certain chronic disease needs to go slowly, which in many ways goes against scientific dogma with its “quick cure with a round of antibiotics.” Both Trevor and I believe bacteria are implicated in sarcoid, even though this is still denied by many physicians who consider sarcoid a “disease of unknown etiology” — and all the research pointing to bacteria in sarcoid is ignored. Trevor obviously believes bacterial infection also plays a role in certain other chronic diseases. If you think about it, diseases like tuberculosis, leprosy and cancer all take years to treat. You don’t necessarily expect to get well in one month, one week, or even one year. Similarly, one shouldn’t expect a quick cure in chronic disease, even though bacteria play a big role in these diseases.

15. What do you feel lies ahead in terms of cancer research?

I feel that the treatment of cancer will remain dismal until these bacteria are recognized as cancer-causing agents by the scientific and cancer establishments. Only then can better treatment methods be employed that actually are specifically directed against the buildup of these L-forms or are directed towards strengthening the immune system against them, or both.

End of interview

You will note that all of the ladies mentioned above were all senior citizens and had dedicated their entire life in finding a cure for cancer which they had achieved but like Dr. Virginia Livingston were never allowed to develop that cure.

It is despicable to know that all those responsible for the health and welfare of their citizens in each respective countries were so deceitful in hiding the cures that these ladies and gentleman had achieved during their working life…….that is a crime against human kind!

No Doubt by now you are all overwhelmed that so many of today’s deadly diseases are bacterium based and can be cured……..including the very deadly Ebola in Africa and MRSA that is so rife in our hospitals.

Dr. Virginia Livingston – The Women who cured cancer

The final Part 6 will cover one other expert that will bring us up to date and also show some convincing forensic evidence that Dr. Virginia Livingston had indeed found a cure for cancer and her Patent that still holds true to this day……….if only they would stop being so greedy and swallow their pride!!

Peter Eyre – 0700 Local Time 19/6/2017

Middle East Consultant – Political Analysis – Investigative Journalist – Broadcaster

 

 

Is there a cure for cancer? You bet there is! Part 4

 

Dr. Virginia Livingston

In this chapter we will look at the more technical side of Dr.Virginia Livingston’s cure for cancer and how she used the Tuberculosis Vaccine (BCG) and her own Autogeneous Vaccine made up with cancer bacterium taken directly from her infected patients tumors, glands, blood or urine all of which acted in the same way as phage treatment is used in Russia for many deadly diseases and infections such as gangrene and MRSA etc.

Before moving on it is important to understand the emphasis that Dr. Virginia Livingston placed on boosting up the patients own immune system, which she explains in her treatment protocol.

Some of her more critical patients had already succumbed to chemotherapy and radiation which she clearly believed was directly responsible for killing off of  a person immune system and made her progress with such patients  extremely difficult.

Dr. Livingston explained that in many of the slaughter houses that produced red meat  cancerous tumors, cells and cancer bacterium existed in many animals.

The same applied to chickens and generally speaking the existence of cancerous tumors, cells and bacteria was at a much higher level……….obviously since those earlier days hygiene has come a long way but one would have to still be cautiously mindful of their possible existence.

Finally one must be aware that as the nucleus of any cancer is bacterium based and is therefore infectious one must take appropriate precautions when taking  samples from tumors, cells, blood or urine and when dealing with the patient themselves!

Dr. Livingston invention made it possible to identify cancer bacterium before the formation of tumors and this was explained by her in this paragraph:

METHODS OF IDENTIFYING CRYPTOCIDES

This invention also involves a test that will show the existence of a neoplastic disease before the tumor exists, or the existence of a chronic underlying infection in man and/or animal. Until now any aberrant symptom of a patient has to be evaluated in the light of a latent cancer until it was ruled out. A fever of unknown origin could turn out to be a sarcoma somewhere in the body made manifest weeks later after much laboratory work and X-rays. By then, it was already too late, to do anything. Even if it had been known that cancer was imminent there was no treatment. There was nothing to do but wait until a tumor presented itself and then attempt to cut it out or destroy it by radiation or chemicals. (Applicants’ invention involves a cure for such cancer.)

Tests for determining the presence of cancer such as the Pap smears tests have serious problems associated therewith. In the Pap smears tests, the body cells that are cast off from the uterus, cervix and vagina are smeared from the cervix, are placed on a slide and stained. Not only is the presence of cancer cells detected but the amount of estrogen in the body is indicated by the size and shape of the nucleus of the cell in relation to the cytoplasm. This test is useful in determining the stage of menopause in women. Unfortunately, when the smear for cancer is positive, the cancer is already there. However, it does permit early detection of some kinds of cancer of the female reproductive organs. The same method of cell determination is now applied to a number of other sites such as lung and stomach.

As cancer is an infection, surgery, radiation and chemicals cannot eradicate a continuing infectious process. For example, cobalt machines may reduce the size of tumors but contribute very little to the long-term cure of the disease.

The test of this invention allows a screening program of the entire population by means of routine blood cultures to determine the presence of the cryptocides bacteria correlated with evaluation of blood smears and related to immune competency by various methods of antigen-antibody determination.

Dr. Livingston makes it clear in her writing that even advanced forms of cancer can be addressed with blood samples being taken from the so called dying patient, cultured in the laboratory and then re introduced back into the patient as an Autogeneous Vaccine…….obviously 100% success is not guaranteed as previous chemotherapy or radiation has to be taken into account and the status of the patients immune system but whatever the circumstances one can but try…..such practices being carried out after the late intervention of cancer victims can be covered under the Declaration of Helsinki.

She further states in her account of Autogeneous Vaccine Preparation the following:

Applicants have prepared and used an Autogenous Vaccine for the treatment of chronic, ongoing infections. Customarily the vaccines are prepared from urine, nasal, throat and bowel secretion as well as from various tissues and other secretions. The vaccines are used for the building up of immunity in the chronically ill patient who suffers from a failure to produce immune bodies against their chronic infection.

“It is now incontrovertible that the cancer disease results in the loss of immunity yet it is treated with radiation which destroys immunity and with drugs which encourage cancerous growth.”

It is clear that Dr. Livingston was not only extremely talented and gifted but had truly found a cure for cancer which to this day has been brushed aside by the greed and might of arrogant Governments, Health Organizations (including the WHO), The Giant Pharmaceutical Industry, Cancer Research Institutions, Cancer Charities, Oncologists and many Doctors who financially benefit in hiding the truth……..one day the truth will come out and this fine lady will be posthumously awarded for her service to humankind!!

Part 5 will introduce other fine pioneers in medicine who agreed with and followed Dr. Virginia Livingston beliefs and who to this day have been severely restricted by all of the above scumbags!!

 

Peter Eyre – 1000 Local Time 17/6/2017

Middle East Consultant – Political Analysis – Investigative Journalist – Broadcaster

 

Is There A Cure For Cancer ? You Bet There Is! – Part 3

Virginia Livingston, MD (1906-1990)

In this part of the story on cancer I can only ask you to look into the face of this wonderful women and not only see a natural loving kindness but also realise that what she had to endure right up to her death in 1990 was unbelievable red tape and ridicule.

Virginia Livingston never gave up on her cancer research and although she continued to learn so much from fellow peers she would have to be the only possible women that actually understood cancer in its many forms and but also knew how to cure it.

This is an amazing story of the woman who put cancer in permanent remission and in doing so not only cured it but also exposed cures for so many other deadly diseases that all had one thing in common “They all had bacterium as there nucleus, all were possibly infectious and all could be cured”

Don’t you find it sad that when a person has gained so much respect in the medical profession, written so many medical journals that were praised by all who read them and then suddenly attacked and ridiculed because she had found a cure for cancer!

All the respective governments, health departments, oncologists, cancer foundations and the massive pharmaceutical industry suddenly went on the attack when they realized that not only had she found a cure but also had the ability to cut their multi billion dollar scam research into “Not finding a cure.”

Hopefully one day this dear lady will receive a well deserved posthumous award for her services to humankind!!

I will first cover her story and then follow up with many other pioneers in the industry who used Virginia protocol in their own research.

Believe me you will be amazed at all the lies and deceit that continue to this day when there has always been a cure, especially when you can identify the cause (Bacterium) which this lucrative industry has covered up for far too long!!

It is time for the truth to come out and time to bring those responsible for this cover-up to go on trial for crimes against humanity……to put it into its true perspective the link between TB- Cancer – HIV AIDS in the Bacterium sense is unbelievable.

It should also be noted that  HIV-AIDS was intentionally introduced into the world’s population via Africa…….just think – more than 25 million people have died including half a million Americans and more than 40 million are currently infected……I could extend this story into another western scam called Ebola and no doubt you will be amazed to find out that there is also a cure for that……and how about the damage being done to African children with highly toxic vaccines….but who’s really interested.

 

I won’t go into who spread HIV AIDS but it is said a certain US military base had perfected Chemical and Biological Warfare…..not forgetting the help of the British in the production of Anthrax and other deadly diseases and gases which were clearly exported around the world and which gave Saddam the ability to poison his own people in Iraq, the Iranians during the Iraq-Iran War and on Coalition Forces during the Gulf Wars….not to mention the labs and the ingredients that were given to him by the west!!!!!

Now back to the wonderful story of Dr. Virginia Livington as provided by many of her associates and admirers:

Dr, Virginia Livingston with another pioneer Dr. Alan Cantwell

The above photograph was taken in 1981 nine years before Dr. Livingston’s death….she continued her research and her fight with the various authorities right up to her passing and who actually commenced to issue a subpoena  the day after her death…….

The following is an extract –

[1983] The Conquest of Cancer: Vaccines and Diet by Virginia Livingston Wheeler M.D. –  Edmond G. Addeo

Virginia C. Livingston–Integrating Diet, Nutritional Supplements, and Immunotherapy

The story of Virginia C. Livingston, a physician who died in her late eighties in 1990, is at once dramatic and prototypical of those who venture off the path of mainstream cancer medicine. After undertaking some exacting research, she claimed that she had discovered a microbe that caused cancer and then developed a vaccine that she claimed would help control that microbe. Whether or not her claim has any validity has not yet been fully evaluated, although it has been categorically dismissed by mainstream medicine.

In addition to her vaccine, Livingston also developed a multifaceted nutritional, medical, and immuno supportive program, which can be traced back in part to the German naturopathic tradition of Max Gerson and Josef Issels. She can therefore be considered a “second-generation” nutritional cancer therapist, especially since fully half of her program is nutritional in content. Livingston’s treatment is still being offered at the Livingston Clinic in San Diego.1

Livingston’s Biography

Virginia Livingston started her medical career as one of the pioneering women physicians of her time. Her great-uncle and father were both physicians, and her father was one of the early members of the American College of Physicians. She was one of only four women to receive her M.D. from New York University in 1936 and was appointed the first woman resident physician at a New York hospital–the prison hospital for venereally infected prostitutes.2

While at the prison hospital, she became interested in tuberculosis and leprosy, which were being treated in nearby infectious disease units. As a school physician a few years later, she became interested in scleroderma, a degenerative disease of the skin and tissue that Livingston came to see as related etiologically to tuberculosis, leprosy, and cancer.

Livingston found that a red dye staining technique revealed numerous “acid-fast” organisms (organisms that stained when exposed to the diagnostic dye) in scleroderma. These organisms, she believed, were similar to those found in leprosy and tuberculosis. Because she saw scleroderma as similar to cancer, she began to wonder whether she might not find similar organisms in cancer tissue. “At this point,” she writes, “I reasoned that perhaps scleroderma was a kind of slow cancer. I decided to begin examining cancer tissues with the same method. … Upon examining all kinds of cancerous tissues … I found that a similar microorganism was present in all of them.”3

Livingston then made contact with Eleanor Alexander-Jackson, M.D., of Cornell University, who had found that the tubercle bacillus undergoes many changes in shape, and hence is “pleomorphic” (able to change shape and size.) At that time, cancer was thought to be caused by a virus, and the technique for differentiating a virus from a bacillus was to see whether it passed through a special filter; viruses are much smaller than bacilli and could pass through the filter. Her association with Alexander-Jackson led Livingston to conceive of the acid-fast organisms she saw in scleroderma, leprosy, tuberculosis, and cancer as a family of pleomorphic organisms that sometimes assumed very small forms similar to viruses and at other times had large forms similar to bacilli.4

Against considerable odds, Livingston was able to develop a research program to explore this world-class research hypothesis: a family of microbes–able to change dramatically in size and shape–were responsible for the development of cancer, tuberculosis, leprosy, and scleroderma. At a time when women physicians were scarcely welcome in leading roles in cancer research–much less as champions of major breakthrough concepts–she created the Rutgers-Presbyterian Hospital Laboratory for the Study of Proliferative Diseases associated with the Bureau of Biological Research of Rutgers University.

She received funds from the American Cancer Society and an impressive group of foundations and medical laboratories. “The next few years at Rutgers,” Livingston writes, “were to be the most significant period of my work in cancer research. Our research team was enthusiastic that our work would prove once and for all that the Progenitor cryptocides [or PC, the name she would later give the organism she believed she had discovered] microbe was the cause of cancer and that a vaccine could be made to defend against it.”5

Alexander-Jackson left Cornell to work with Livingston at the new laboratory, and they built a small research team. In 1950, she and Alexander-Jackson published a paper in the American Journal of Medical Sciences, which was co-authored by four others including James Hillier, developer of the electron microscope and head of electron microscopy at RCA Victor Laboratories in Princeton, and John Anderson, head of the department of bacteriology at Rutgers and a noted histologist and pathologist. In this paper, they described how Koch’s postulates (“the accepted foolproof method of proving the cause of a disease”) could be satisfied in the case of P. cryptocides. Pure P. cryptocides cultures were obtained from both human and animal cancers and injected into animals capable of being infected. Disease areas then developed resembling those from which cultures were taken. Pure cultures were then re-isolated from the infected animals. “Koch’s postulates,” Livingston writes, “were fulfilled to the satisfaction of our entire group and to that of our biology superiors at Rutgers.”6

Livingston had thus demonstrated to her own satisfaction, and to that of some colleagues, that she had isolated a microorganism that caused cancer in both animals and humans. Needless to say, for Livingston and anyone who credited her discovery, this was a historic accomplishment. “The next step,” she says,

was to prove that the cancerous growth was not the whole disease. For more than one hundred years people like Rudolf Virchow thought that cancer cells themselves were parasites within the body. He did not understand that the small coccuslike granules he saw dividing in the cancers were not the development of daughter cells within mother cells, but instead they represented the true intracellular parasite that was the causative agent. … The whole truth may be that the parasite within the cancer cell transforms the normal cell into a sick cell that cannot mature by normal cell growth processes. In other words, the tumor is not the disease.7

Her claims did not, however, find approval in the medical community. In 1953, a spokesman for the New York Academy of Medicine, Dr. Iago Gladston, discounted her claims, echoing the attitude of most of the medical community. “This is an old story,” he said, “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.”8

That Livingston’s bold thesis did not find approval in the medical community is not surprising, but the strong opposition to allowing her to continue her efforts to develop and defend her thesis was scientifically unconscionable. As a result, Livingston’s laboratory in New Jersey was forced to close in 1953 due, according to her, to the efforts of leading researchers at Memorial Sloan-Kettering Cancer Center in New York opposed to her research.9 Deeply disappointed, Livingston moved to California to live near her family. But in Europe, and within a small faction of the microbiology research community in the United States, interest in theories similar to hers continued to develop.

Livingston became an Associate Professor of Microbiology at the University of California in San Diego to continue her research. In 1969, she and Alexander-Jackson and their colleagues presented a group of papers at a New York Academy of Sciences meeting on “microorganisms associated with malignancy.” Some of the articles were published in the Annals of the New York Academy of Sciences.10

Livingston viewed P. cryptocides as what she called an “obligate symbiont”: an organism necessarily present in all human cells, in fact one that plays a vital role in all reproductive life, including fertilization and pregnancy and the development of the cancer cell.11 But this obligate symbiont is susceptible to a malignant transformation and proliferation in disease states, especially those that depress normal immune function. She saw cancer as an immunodeficiency condition caused by environmental toxins and inadequate diet.12

In other words, in the classic dispute between researchers who give primary importance to the infectious agent in a disease and researchers who believe that the infectious agent only takes hold in an organism weakened by poor nutrition, toxins, or other stressors, Livingston came down in the middle. The agent did, she believed, play a critical role: it could be isolated and a vaccine effective for the prevention of cancer and modulation of existing cancer could be developed. But the weakened terrain of the organism was also critical, for it provided the depleted environment in which the infectious agent took on pathological shape and multiplied out of control.

In 1990, the Office of Technology Assessment summarized the prevailing attitude about Livingston’s work within the research establishment:

[Dr. Livingston has] little support, outside of a few researchers, for her belief that the different microbes observed in the tissue and blood of cancer patients are actually different forms of the same microbe. At present, no independent evidence exists to corroborate her contention that the microbial forms are related to each other as different forms of a single, pleomorphic organism. Evidence does show that the bacterial culture Livingston isolated is not a new and unique species as claimed: P. cryptocides supplied by Livingston were identified as different species of the genus Staphylococcus and Streptococcus. The issue of isolating bacteria of any kind from tumor tissue and urine of cancer patients, however, is generally not disputed, since many groups of researchers have reported isolating various species and strains of bacteria from such sources. Some of these bacteria have also been showed to undergo morphogenic alterations characteristic of cell wall deficient (or pleomorphic) bacteria.13

It should be noted that the same author has also written another book about Dr.Livingston: 

The Woman Who Cured Cancer: The Story of Cancer Pioneer Virginia Livingston-Wheeler, M.D. and the Discovery of the Cancer-Causing Microbe

by Edmond G. Addeo

In Part 4 I will continue to reveal the incredible work carried out by Dr. Virginia Livingston and work carried out by other medical pioneers who supported not only Dr. Livingston Protocol but also agreed with her research into the connectivity between TB – Cancer-HIV AIDS and many other bacterium based diseases.

 

Where does all the money go – “God Know’s

It will become clear to you all that governments – health departments – oncologists – cancer foundations/charities and the big pharmaceutical industry have indeed created their own scam in raising billions of dollars in “Not Finding A Cure For Cancer.”

Peter Eyre – 0840 Local Time – 15/6/2017

Middle East Consultant – Political Analysis – Investigative Journalist – Broadcaster

 

 

 

 

 

Is There A Cure For Cancer ? You Bet There Is! – Part 2

Lets start by opening up a can of worms and expose the worldwide cancer scam

One of the biggest investment banks in the world

 

In my last article I covered the basic understanding of what cancer actually is and how it is related to many other serious diseases all of which have Bacterium as their nucleus.

We must fully understand that our respective governments, health departments, oncologists, cancer research institutes, cancer charities, the very lucrative pharmaceutical industry and their “Zionist Controlled Media” are literally making a killing (both financially and physically speaking) in their multi billion dollar scam “In not wanting to find a cure for cancer.”

Who controls the pharmaceutical industry & World Health (WHO) can kill us all

 

What we know so far and the factual connection between many deadly diseases is that they not only have something in common but they can all be cured by the application of simple medical logic!

Imagine being a cancer victim having suffered their extremely painful and expensive chemotherapy and being pumped up with untold concoctions of medication and morphine only to be told there is nothing more we can do for you!

Imagine being lied too from day one that your cancer is not what they think it is and that it is a bacterium similar to Tuberculosis and although contagious can be cured!

Imagine having multiple operations on your leg, pins or plates inserted and then after many years being told it has become badly infected and that gangrene has set in and now consequently you will have to have your leg amputated when once again a simple medical procedure could have saved it!

Practically speaking it all comes down to simply accepting that bacterium is the root cause of many of today’s more serious diseases and thus if one treats it as a bacterium, identifies that bacterium and reintroduces that bacterium back into the patient you are basically creating an anti venom in much the same way as a snake bite!

You would be shocked if you actually knew the bacterial connection between many of what the scumbags call deadly diseases and how so many innocent victims have passed away (in their millions) when they could have been saved by treating the root cause as bacterium based!

Let’s now link some of these so called deadly diseases, connect the dots and prove that we are all being truly conned in their analysis whilst at the same time being ripped off for medication that we did not require had their analysis been correct in the first place!

We are being ripped off an arm and a leg

The following is an initial list of terrible diseases that have a common bacterium link:

Leprosy, tuberculosis, cancer, scleroderma, Raynaud’s syndrome with a strong possible connection to AIDS.

Couple the above to another relatively unknown treatment called “Phage” for other deadly bugs such as MRSA or badly infected limbs and tissue etc and one can clearly see that our government, health professionals, consultants, oncologist, doctors and pharmaceutical industry either simply do not understand what is causing the problem or alternatively simply refuse to accept for fear of impacting on their multi billion dollar industry, their own ex gratia payment or salary top up etc.

To give you all some idea of the alleged success rate lets look at some figures in regard to cancer treatment that was carried out some time ago by a certain doctor who had been working on cancer for decades and who’s initial work was applauded in her many medical journals only to be ridiculed and closed down when they realized she may well have a cure for cancer…….such is the state of affairs in this very lucrative practice in pretending to find a cure whilst raking in billions of dollars but never finding one!

62 random patients were chosen for her trial whilst accepting that cancer was bacterium based and could be treated with bacterium extracted from each patient, cured in the lab and re introduced back into the patient. This extraction was from the tumor, tissue, gland, blood or urine…….remembering another false declaration by the industry that “Blood is not sterile.”

The 62 patients consisted of the following (Included were 17 patients officially diagnosed as terminal):

The 62 cases included 21 breast cancer patients of various types, 5 lung cancer patients, 3 uterine cancer, 3 ovarian cancer, 6 colon cancer, 6 melanoma, 2 basal cell skin cancer, 3 prostate cancer, 2 kidney cancer, 1 pancreatic cancer, 1 pelvic cancer, 1 esophageal cancer, 1 larynx cancer, and 6 Hodgkin’s disease patients.

In summarizing these cases, she officially claimed, “an examination of the sixty-two random cases shows that our success rate has been 82%. Considering the patients we called inconclusive but for whom we were able to be of some help, it is over 90%”

I also understand that she also drew attention to the fact that her success rate would have been higher had some of them not been treated by chemotherapy or radiation which directly  attacks the immune system that is so vital in the recovery of patients!

One can see that our governments, departments of health and the thousands of specialists employed in the above and the pharmaceutical industry really do need to be re educated and exposed for their Weapons of Mass Deceit (WMD) and in some cases placed before the court system to be tried for what they are “Deceitful Imbeciles.”

If you think that this is bad wait till I uncover the same deceit in regard to the world’s vaccination programmes promoted by the New World Order and its puppet the United Nations/WHO under UN Agenda 21 and its replacement programme UN 2030 Agenda to depopulate the world by as much as between 80-90% of current population “by whatever means” and how the ingredients and adjuvants in those vaccines are causing death, maiming, mental deterioration, dumbing up and infertility to our babies, very young and our teenagers…….all of which has been approved and countersigned by our respective governments……some of whom are directly or indirectly benefiting financially  by their own investments!!!!

 

Part 3 will be a more technical brief to reveal the fine work carried out by many superb doctors, who they were, what they found and how they were treated by the above mongrels and finally show that “a cure for cancer and other deadly diseases does exist.” 

Peter Eyre 0930 local time 13/6/2017

Middle East Consultant – Political Analysis – Investigative Journalist – Broadcaster

 

 

 

 

 

 

 

 

 

 

Is There A Cure For Cancer ? You Bet There Is! – Part 1

 

Over many many years I have tried to understand why they have not found a cure for cancer when billions of dollars continue to be pumped into the many research institutes each and every day throughout the world without a ray of hope being given for the millions of innocent victims who trust their governments, hospitals, cancer clinics, oncologists and cancer organisations in saving them from this terrible disease .

Historically many gifted professors and doctors have hit the cause of cancer on the head but in doing so have been immediately silenced by governments health departments. pharmaceutical companies or cancer institutes by either ridicule or simply having their licence revoked or their potential cure shelved by those who make far more money in not finding a cure!

Why would anyone in their right mind wish to cause so much pain and suffering to the victims of cancer when many extremely talented doctors had looked upon cancer in a totally different light and provided potential treatment that did not harm the body, as radiation and chemotherapy do. 

 

Who in their right mind would allow the bodies natural immune system to be bombarded with radiation and chemotherapy whilst at the same time giving their patients high doses of morphine to a point that one would have to ask the question as to what actually killed the patient in their final days.

How would you feel if you had cancer or your loved one had cancer and were told that the existing understanding of the origins of cancer were all wrong and that all those mentioned above were covering up the real truth as to what is cancer or what causes cancer to develop?

How would you feel if you found out that cancer was closely linked to other serious illness’s such as Tuberculosis (TB) or HIV AIDS etc and was bacterium based and that a potential cure was available?

How would you feel if you were told that HIV AIDS was first intentionally introduced into the world’s civilian populations by the US Military and had no connection to monkey’s or apes?

I know it did not come from me so how come you have become so gullible you believe such bullshit?

 

So lets now look at cancer from a different perspective and think of it as being bacterium based and accordingly consider that it can now be passed on to someone else i.e. infectious but also fully understand that it is also curable!

Some very notable researchers, who have had their achievements printed in medical journals, came across some very unusual findings in their respective laboratories, suffice to say they all agreed that cancer was indeed a bacterium!

It was during my years of research that I also came across the use of “Phage” to combat some very serious conditions such as MRSA that now exists in many of the world’s hospitals and for which there was no apparent cure……….but there is!

Let me put this to you in a very simple way:

If you are bitten by a snake the hospital identifies the culprit, finds the same venom and use it as a anti venom to put back into your already contaminated body to fight the same venom or bacteria.

In a nutshell if we are infected with bacterium in any form then if one is able to find that same bacteria either by extraction from the victim or find the same bacterium in its natural environment, take it back into the lab and create a microbiological culture and eventually re introduce that bacterium back into the patients body makes perfectly good sense!

One must also keep in mind the United Nations Agenda 21 and its replacement UN 2030 Agenda regarding mass depopulation by whatever means (which has been countersigned by many countries) is clearly targeting the world’s population via their approved fast track vaccination programmes, unwillingness to cure treatable diseases and using measures that are clearly detrimental to ones health!

In Part 2 we will further explain just how closely linked many of today’s diseases are and prove that their nucleus is bacterium based along with the research carried out  by some notable medical practitioners who’s experience cannot be challenged!

Peter Eyre

Middle East Consultant – Political Analysis – Investigative Journalist – Broadcaster

 

 

 

 

 

 

US Military bases in Australia and their disrespect for our environment

Just look at what past/current Australian Prime Ministers and
our Government have allowed to happen to this beautiful country:

Since the inauguration of John Howard and all subsequent PM’s, these morons, have allowed the US, allies and our own military to test fire their latest uranium based weapons on Australian soil. Our government created live weapons firing ranges at various locations including one in a marine national park on the Barrier Reef!!!!! My bone of contention is the fact that the US Military have been kicked out of many countries as a direct result of contaminating foreign soils with depleted uranium (one of the main incredients in todays weaponry) and in doing so are now contaminating the citizens of Australia, animals, plants, soil and water.

The half life of depleted uranium is 4.5 billion years (almost the same age as planet earth) and cannot be cleaned up.

It directly attacks the very DNA of life itself and once detonated spreads millions of radioactive nano particles into the surrounding environment before drifting on the wind to the rest of Australia, adjacent countries and the world beyond.

Depleted Uranium is in direct violation of the Geneva Convention on at least four counts and consequently should never be allowed in this country or any other country!!

So where are these wonderful environmental hot spots?

Number one on the list for the US Marine Air-Ground Task Force based in Darwin (at the local Robertson Barracks) and for our own RAAF aircrews is Delamere Air Weapons Range which is one of three such ranges in the top end of Australia…….it was so intereting to note one reporters comment when he said “Luckily the Northern Territory provides ample space and facilities to conduct the live firing exercises that modern armies need.” “Delamere Air Weapons Range is the smaller of three live firing areas that the Australian – and many other – military forces have used in the Top End for some time.” and then this comment from the RAAF themselves: “Australia’s premier spot to drop bombs.”

“Delamere is undoubtedly the premier air weapons range in Australia; all Aussie aircrew as well as visiting ones acknowledge that. The fact that we can provide the facilities we do and have virtually unrestricted airspace provides terrific training value for them.”

“We’re totally surrounded by cattle properties and there’s no major air routes that come through here, so strike aircraft have a freedom to practice tactics that is not readily available elsewhere,” “They’ve got 200,000 hectares of ground space out here”

Note that last comment about being totally surround by beef country……”adds new meaning to having a steak on the barbie that may well glow in the dark.”

Then we have the Bradshaw Range which about the size of Belgium also up in the top end and listed as follows: Bradshaw Field Training Area which is on the National Heritage List…..oh really!!……… covers approximately 871,000 ha and is located near Timber Creek, 600km by road south-west of Darwin in the Northern Territory. The training area is bound to the north by the Fitzmaurice River and Wombungi Station, to the west by the Joseph Bonaparte Gulf, by the Victoria River to the south, and to the east by pastoral properties.

Then we have Mount Bundey Training area up the top end, a 117300 ha. site,75km south-east of Humpty Doo, south of the Arnhem Highway, between the Mary River and Kakadu National Park. Previously a cattle station, the property was acquired as a training area in 1988.

United States and Singaporean forces both conduct joint tank exercises with Australian forces at the MBTA, including the use of an Urban Operations Training Facility constructed in 2005.

Who really cares who blasts away at our country or who contaminates our environment?

Australia now contains major US bases and facilities who’s only purpose is to act as forward operational bases to carry out acts of war/conflicts against countries within the SE Asia region, including China and has nothing to do with national defence…..that makes Australia a major target in any conflict against the US!!!

I guess the crocs and all the other species in the top end will be the first to know…..not to mention the Aboriginal populations…….I am sure we all know what the US did with its own indiginous population!!!

 

Then we have our favorite pristine Great Barrier Reef area and the attached Marine National Park attached to Townshend Island which is a major military training area and bombing range in the Rockhampton area:

The northern part of the zoning area forms part of the Shoalwater Bay Military Training Area (SWBTA). The training area was acquired by the Commonwealth Government in 1965 for defence training purposes. The
area has considerable strategic importance to the Department of Defence being the only location on the east coast of Australia where large-scale joint and combined exercises can be conducted. The training area is managed by the Australian Army from a base in Rockhampton but is also used by the Australian Navy and Air Force as well as overseas forces.

A number of sites within the training area are used for landing by military amphibious vessels and landing craft. These include Freshwater Bay and South Arm which is in Port Clinton. Sea Hound Hard on the south arm of Port Clinton is one of only two locations which can accept heavy landing craft. The other is located on Townshend Island in Shoalwater Bay which is outside the zoning area……..note that Townshend Island does however form part of our Marine National Park.

Townshend Island and the adjacent inland Mount Hummock are both used as bombing ranges as well as the entire region being used as one of the most important War Games areas

One of the biggest major exercise carried out in the Shoalwater Bay region is exercise Talisman Sabre involving US nuclear-powered ships and submarines. The US fleet also carry nuclear weapons as well as depleted uranium munitions.

I am sure we all agree with self defence of our country but certainly not to be taken over by the US forces and other allied armies who only purpose is to continue creating a permanent war/conflict scenario not to mention the deplorable permanent contamination of our beautiful country.

   

So there you have it……..Australia has basically become part of NATO which is the military arm of the New World Order and its only a matter of time before our country becomes totally contaminated by these ongoing war games and that Australia becomes part of the United States permanent war against non existant terrorism.

Finally we must always remember our government telling us about the defecit and in imposing austerity measure on the poor and yet they have an open wallet for purchasing military hardware (including new obsolete fighters) and participating in these extremely expensive war games.

Peter Eyre

Middle East Consultant – Political Analysis – Investigative Journalist – Broadcaster

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

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

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
“In 1951, the CIA decided to coordinate efforts with the US Army, Navy, …. at http://www.mindcontrolforums.com/radio/ckln-hm.htm CKLN42A.tx Sue Arrigo, …
http://www.ecapc.org/Registry_detail. asp?Type=Ind&ContactID=2171 – 32k – Cached – Similar pages

TvNewsLIES.org :: View topic – Female CIA agent who stood up to …
The assignment Cheney gave me was to go to Iran as a physician in a humanitarian gesture to treat … Sue Arrigo, MD California medical license G 50197 …
tvnewslies.org/phpbb/viewtopic.php?t=6461& sid=935c8b88071f6e893ab7650a3d92f492 – 62k – May 31, 2007 – Cached – Similar pages

Military and Civilian Perspectives on the Ethics of Intelligence-
A physician at the workshop, Sue Arrigo (my sister), discussed medical …. by the CIA and the usurpation of military resources for CIA operations [1973, …
http://www.usafa.af.mil/jscope/JSCOPE01/Arrigo01.html – 171k – Cached – Similar pages

AlterNet: Rights and Liberties: The Torture Test
Recent revelations of CIA-run secret prisons abroad has put the issue of torture front and center …..
Sue Arrigo, MD California medical license G 50197 …

http://www.alternet.org/rights/27771/ – 77k – Cached – Similar pages

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
No information available from this agency

Misdemeanor Conviction
No information available from this agency

Administrative Citation Issued
No information available from this agency

Hospital Disciplinary Actions
No information available from this agency

Malpractice Judgment
No information available from this agency

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

All information provided by the Department of Consumer Affairs on this web page, and on its other web pages and internet sites, is made available to provide immediate access for the convenience of interested persons. While the Department believes the information to be reliable, human or mechanical error remains a possibility, as does delay in the posting or updating of information. Therefore, the Department makes no guarantee as to the accuracy, completeness, timeliness, currency, or correct sequencing of the information. Neither the Department, nor any of the sources of the information, shall be responsible for any errors or omissions, or for the use or results obtained from the use of this information. Other specific cautionary notices may be included on other web pages maintained by the Department. All access to and use of this web page and any other web page or internet site of the Department is governed by the Disclaimers and Conditions for Access and Use as set forth at California Department of Consumer Affairs’ Disclaimer Information and Use Information.

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 – Broadcaster