Category Archives: Virus Isolation Technique

What Do Exosomes and Viruses Like HIV & Corona Have In Common?

Dr. James Hildreth PhD MD, proposed that “the virus is fully an exosome in every sense of the word.” [1]

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What Are Exosomes?

Exosomes are membrane bound extracellular vesicles (EVs) that are produced in the endosomal compartment of most eukaryotic cells.[2][3][4] The multivesicular body (MVB) is an endosome defined by intraluminal vesicles (ILVs) that bud inward into the endosomal lumen. If the MVB fuses with the cell surface (the plasma membrane), these ILVs are released as exosomes. In multicellular organisms, exosomes and other EVs are present in tissues and can also be found in biological fluids including blood, urine, and cerebrospinal fluid. They are also released in vitro by cultured cells into their growth medium.[5][6][7][8]

Since the size of exosomes is limited by that of the parent MVB, exosomes are generally thought to be smaller than most other EVs, from about 30 to 150 nanometres (nm) in diameter: around the same size as many lipoproteins but much smaller than cells.[5] Compared with EVs in general, it is unclear whether exosomes have unique characteristics or functions or can be separated or distinguished effectively from other EVs.[2] EVs including exosomes carry markers of cells of origin and have specialized functions in physiological processes, from coagulation and intercellular signaling to acidic waste management of the intravascular and interstitial fluids of the Interstitium – the largest organ of the human body.[5]

Are Exosomes Viruses?

There is NO scientific evidence from ANY research (published or otherwise) from ANY scientist or group of scientists any where in the World validating the existence of the so-called invisible virus or that exosomes have been proven to be the existence of any virus!

Exosomes are created endogenously by the cells, even the red blood cells as a means of mediating or buffering metabolic, environmental, dietary and/or respiratory acidic waste in order to maintain the delicate pH balance of the intravascular fluids, the interstitial fluids and the intracellular fluids of the body cells at 7.365.[9]

Are Exosomes the Agents to the Activation of the Immune System and a Defense Against Metabolic Acids?

What may appear as viral particles are many times indistinguishable from exosomes.

Exosomes are natural micro-vesicles produced by cells; they carry messages from cell to cell, and to other tissues, and possibly to other people. They are essential to health because they carry acidic waste out of damaged cells and trigger the lymphocytes to release reduced oxygen (SO-) and reduced hydrogen (OH-) molecules to buffer metabolic acidic cellular waste to prevent the death of the body.

Are COVID-19 and HIV Exosomes?

Based upon electron microscopy the so-called COVID-19 virus and the the so-called HIV virus are 100 nm in diameter and appear identical to exosomes.

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Endogenously Created Exosomes Protect the Cells

In January 18th of 2020, three scientists published a scientific paper describing the protective purpose of exosomes, entitled, “Exosome-Mediated Transfer of ACE2 (Angiotensin-Converting Enzyme 2) from Endothelial Progenitor Cells Promotes Survival and Function of Endothelial Cell.”[9]

Research on Exosomes and Their Support of the Lymphocytes (Immune System) in Reducing Cancer-causing Acidic Waste

Exosomes from red blood cells contain the transferrin receptor which is absent in mature erythrocytes. Dendritic cell-derived exosomes express MHC I, MHC II, and costimulatory molecules and have been proven to be able to induce and enhance antigen-specific T cell responses in vivo in reducing metabolic acidic waste.[10]

What Is the Relationship Between Exosomes and COVID-19

They both contain the ACE2, or angiotensin converting enzyme-2 receptor and visually, using an electron microscope measure the same size. The exosomes or should we say the COVID-19, ACE2 receptor chops up two forms of a protein called angiotensin to keep blood pressure stable by protecting cell membranes from cellular breakdown from metabolic, dietary, environmental and respiratory acidic waste.[9]

So What is Causing the Symptoms of COVID-19 and the Release of Exosomes into the Extracellular Matrix?

It is a four letter word – ACID! Where is the ACID coming from?

The major contributing factors that cause cellular breakdown and the release of exosomes into the extracellular matrix are as follows:

1. Electro-magnetic pulsating frequencies ranging from 1GHz to 600GHz.[11][12][13]

2. Carbon Dioxide and Monoxide Poisoning.[14][15][16][17][18][19]

3. Glyphosate Acid Poisoning from non-organic fruit and vegetables.[20][21]

4. Lactic Acid Poisoning from diet and metabolism.[20]21]

5. Uric, Nitric, Sulphuric and Phosphoric Acid Poisoning from eating the flesh and blood of animals.[20][21]

6. Genetically Modified Organisms in our food supply and vaccines.[20][21]

7. Aluminum Oxide Poisoning from vaccination and chem trails.[24]

8. Antibiotic Poisoning.[22][23][24]

9. Acidic Polluted Water, Alcohol, Coffee, Black tea, Soda drinks, Sport drinks.[20][21]

10. Sugar in all of its form or any word that ends in ‘ose’.[20][21]

How Can I Support the Alkaline Design of the Body and Reduce Metabolic, Dietary, Environmental and Respiratory Acidic Waste that is Making Me Sick and Tired?

First, read five books by Dr. Robert O. Young to start with –

1. Sick and Tired, Reclaim Your Inner Terrain[20]

2. The pH Miracle revised and updated[21]

3. Chlorine Dioxide (CLO2) As a Non-Toxic Antimicrobial Agent for Virus, Bacteria and Yeast (Candids Albicans)[22]

4. Alkalizing Nutritional Therapy in the Prevention and Treatment of any Cancerous Condition,[23] and,

5. Second Thoughts about Viruses, Vaccines, and the HIV/AIDS Hypothesis.[24]

Second, follow the protocol as outlined in Chapter 5 and 11 in The pH Miracle Revised and Updated for at least 12 weeks.[21]

Third, If you need further clarification and support you can setup a consultation with Dr. Robert O. Young by clicking here: https://www.drrobertyoung.com/services-page

Fourth, you can attend a pH Miracle Retreat and immerse yourself in a paradise of alkalinity. To learn more go to: www.phmiracleretreat.com

References

[1] https://rupress.org/…/6/9…/33690/When-is-a-virus-an-exosome…

[2] Théry C, Witwer KW, Aikawa E, Alcaraz MJ, Anderson JD, Andriantsitohaina R, et al. (2018). “Minimal information for studies of extracellular vesicles 2018 (MISEV2018): a position statement of the International Society for Extracellular Vesicles and update of the MISEV2014 guidelines”. Journal of Extracellular Vesicles. 7 (1): 1535750. doi:10.1080/20013078.2018.1535750. PMC 6322352. PMID 30637094.

[3] Yáñez-Mó M, Siljander PR, Andreu Z, Zavec AB, Borràs FE, Buzas EI, Buzas K, et al. (2015). “Biological properties of extracellular vesicles and their physiological functions”. Journal of Extracellular Vesicles. 4: 27066. doi:10.3402/jev.v4.27066. PMC 4433489. PMID 25979354.

[4] van Niel G, D’Angelo G, Raposo G (April 2018). “Shedding light on the cell biology of extracellular vesicles”. Nature Reviews. Molecular Cell Biology. 19 (4): 213–228. doi:10.1038/nrm.2017.125. PMID 29339798.

[5] van der Pol E, Böing AN, Harrison P, Sturk A, Nieuwland R (July 2012). “Classification, functions, and clinical relevance of extracellular vesicles”. Pharmacological Reviews. 64 (3): 676–705. doi:10.1124/pr.112.005983. PMID 22722893.

[6] Keller S, Sanderson MP, Stoeck A, Altevogt P (November 2006). “Exosomes: from biogenesis and secretion to biological function”. Immunology Letters. 107 (2): 102–8. doi:10.1016/j.imlet.2006.09.005. PMID 17067686.

[7] Spaull R, McPherson B, Gialeli A, Clayton A, Uney J, Heep A, Cordero-Llana Ó (April 2019). “Exosomes populate the cerebrospinal fluid of preterm infants with post-haemorrhagic hydrocephalus”. International Journal of Developmental Neuroscience. 73: 59–65. doi:10.1016/j.ijdevneu.2019.01.004. PMID 30639393.

[8] Dhondt B, Van Deun J, Vermaerke S, de Marco A, Lumen N, De Wever O, Hendrix A (June 2018). “Urinary extracellular vesicle biomarkers in urological cancers: From discovery towards clinical implementation”. The International Journal of Biochemistry & Cell Biology. 99: 236–256. doi:10.1016/j.biocel.2018.04.009. PMID 29654900.

[9] Wang J, Chen S, Bihl J, “Exosome-Mediated Transfer of ACE2 (Angiotensin-Converting Enzyme 2) from Endothelial Progenitor Cells Promotes Survival and Function.” Oxid Med Cell Longev, 2020 Jan 18;2020:4213541. doi: 10.1155/2020/4213541

[10] Mignot G, Roux S, Thery C, Ségura E, Zitvogel L (2006). “Prospects for exosomes in immunotherapy of cancer”. Journal of Cellular and Molecular Medicine. 10 (2): 376–88. doi:10.1111/j.1582-4934.2006.tb00406.x. PMC 3933128. PMID 16796806.

[11] Rubik, B. Bioelectromagnetic Medicine. Administrative Radiology Journal XVI(8), August 1997, 38-46.

[12] Young, R.O., “The Effects of ElectroMagnetic Frequencies (EMF) on the Blood and Biological Terrain.” https://www.drrobertyoung.com/…/the-effects-electromagnet-f…

[13] Young, R.O., “Adverse Health Effects of 5G Mobile Networking Technology Under Real-Life Conditions.” April 19th, 2020. https://www.drrobertyoung.com/…/adverse-health-effects-of-5…

[14] NOAA. (2016). In a high carbon dioxide world, dangerous waters ahead. (accessed on August 6, 2019)

[15] NOAA. (2018). What is Ocean Acidification? (accessed on August 6, 2019)

[16] National Geographic. (2017). Ocean Acidification. (accessed on August 6, 2019)

[17] NOAA. (2010). Ocean Acidification, Today and in the Future. (accessed on August 6, 2019)

[18] Young, R.O., Young, S.R, “The pH Miracle Revised and Updated.” Hachett Publishing, 2010.

[19] Are the Interstitial Fluids Raining Acid on YOUR Lung Cells? (December 17th, 2019)

[20] Young, R.O., “Sick and Tired.” https://www.phmiracleproducts.com/…/books-audio-video/produ…

[21] Young, R.O., Young, S.R. “The pH Miracle Revised and Updated.” Grand Central Publishing, NY, NY, 2010. https://www.phmiracleproducts.com/…/the-ph-miracle-revised-…

[22] Young, R.O.,”Chlorine Dioxide (CLO2) As a Non-Toxic Antimicrobial Agent for Virus, Bacteria and Yeast (Candids Albicans),” Hikari Omni Media, August 2nd, 2016. https://www.phmiracleproducts.com/…/chlorine-dioxide-clo2-b…

[23] Young, R.O., Migalko, G., “Alkalizing Nutritional Therapy in the Prevention and Treatment of any Cancerous Condition.” Hikari Omni Media, August 1st, 2016. https://www.phmiracleproducts.com/…/alkalizing-nutritional-…

[24] Young, R.O., “Second Thoughts about Viruses, Vaccines, and the HIV/AIDS Hypothesis,” Hikari Omni Media, August 2nd, 2016. https://www.phmiracleproducts.com/…/second-thoughts-about-v…

The Corona Virus is Just a Concept That Only Exists on Paper

In 1960 a veteran retro virologist urged his peers to “raise questions whether the known facts about viruses suffice to account for it.” The subject was cancer, the veteran was Peyton Rous, and the quote is from a paper in Cancer Research. Mindful of that example, in 198I, asked a similar question in a paper likewise published in Cancer Research: whether the known facts about two human retroviruses suffice to account for Leukemia and AIDS.

Clearly, following Rous’s example did not make me very popular with the multinational club of retro virologists. My article was officially ignored and not “dignified” with a response because the AIDS virus establishment was “too busy . . . saving lives” and testing for antibodies to HIV – just like they are doing today with the phantom corona virus or COVID-19.

I was often shunned like an AIDS patient by my former fellow microbiologists and virologists. My views were unwelcome for several reasons: after a frustrating, twenty-year-long search for a human cancer microbe, the retro virologists were craving for clinical relevance and hence happily adopted HIV – ‘the AIDS virus’ -as the cause of AIDS. The discovery of HIV was announced in the U.S. at a press conference and the virus-AIDS hypothesis became instant national dogma. On this basis, the retro virologists convinced their governments to spend billions of dollars to stop the predicted viral epidemic, already being labelled “the epidemic of the 20th century.” Does all this sound familiar with what is happening today with COVID – 19?

The Viral Theory Was The Immediate Darling of the Biotechnology Companies

Due to its very low complexity, it can be readily cloned for diagnostic test kits and vaccines. In turn, the virus was a hit with the press because it mobilized in their readers the instinctive fears of a contagious disease, and appealed to the public prejudice that all evil comes from without.”

Where is the Proof?

Perhaps the foremost thing that should be said about HIV or for that matter any virus is that they have never been proven to be the cause of AIDS, or any human illness. Not one scientific paper exists that demonstrates it. This is also the case with Ebola, Zika and now SARS COVID-2 and 19!

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Based on activity in contrived situations in test tubes, among other illogical things, its culpability was a pronouncement handed down by an authority figure at the National Institute of Health. It is the same authority (Dr. Robert Gallo, head of NIH cancer labs removed from his position for scientific fraud) behind the expenditure of around a trillion dollars in cancer research which has produced NOTHING but an epidemic that is virtually out of control. (One wonders what it will take before people finally get the idea and stop creating walks, rides, telethons and cake sales to contribute money to the bottomless pit of biased, misdirected, wasteful and cruel orthodox medical research in cancer, degenerative disease and virology.)

And, it is the same authority who has taken out two patents whose value depends upon HIV or COVID – 19 as being accepted as the cause or a co-factor. One patent is for the technique of testing for the virus, and the other for a method of laboratory cultivation. No one in a position to do anything about it questions this obvious conflict of interest. This is going on right now today with the testing of an antibody without ever identifying isolating, purifying and culturing the virus, COVID-19.

Kary Mullis, PhD, Nobel laureate in chemistry for his invention of the Polymerase Chain Reaction (PCR) for testing genetic matter, stated, “I can’t find a single virologist who will give me references which show that HIV is the probable cause of AIDS …. If you ask a virologist for that information, you don’t get an answer, you get fury” [1]. Dr. Mullis has continued his outspoken criticisms of the AIDS establishment, “Where is the research that says HIV is the cause of AIDS? We know everything in the world about HIV now. There are 10,000 people in the World now who specialize in HIV.”

This same fraudulent activity in virology has continued with the Ebola virus, the Hantavirus, the Hepatitis virus, the West Nile virus, the Zika virus, just to name a few, and now with the Corona virus – COVID -19, which is an acronym that stands for, “Certificate Of Vaccination Identification (C.O.V.I.D.) – Artificial Intelligence (1 represents the first letter in the alphabet = A and 9 represents the ninth letter in the alphabet = I).

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Most virologist have very little interest in the possibility that HIV doesn’t cause AIDS or that the Corona virus doesn’t cause hypoxia that leads to acute respiratory disease syndrome or ARDS, because if it doesn’t, their expertise is useless. [2] Their embarrassment, humiliation and scientific fraud would also be considerable!

Just look what happened to Dr. Luc Montagnier, a virologist, for his non-discovery of the HIV virus, for which he received a Nobel Prize in Medicine without ever isolating the HIV virus under the scientific method of Koch’s Postulates and Farr’s law (see below for more information on Koch Postulates and Farr’s law).

Dr. Montagnier just recently inaccurately claimed that the phantom coronavirus is man-made and contains genetic material (GMO) from HIV which doesn’t even exist! So how does a virologist take genetic matter from HIV or a Corona virus or any other virus for that matter which has never been isolated, purified and genetically and biochemically identified?

NOW Take A Deep Breath

Just take a moment and take a deep breath and consider what if what I’m telling you is 100 percent true and it is only the tip of the iceberg?

Please, Please, Please do your own research! – Stop being a Sheep

First, start by reading, “Inventing the AIDS Virus” by Peter Duesberg, a Retro Virologist at The University of California Berkley.

Second, read Nobel laureate Kary Mullis, PhD book, “The Polymerase Chain Reaction” (PCR). Dr. Mullis does not see the relevance for testing antibodies by PCR when the virus such as HIV or COVID – 19 have not been isolated, purified, genetically and biochemically tested and then viewed under electron microscopy. Once these steps have been completed, the isolated and purified virus needs to be tested again by following the scientific method for verification of any disease causing germ. The tests are called Koch’s postulates and Farr’s law.

The Virus and Koch’s Postulates

Koch’s postulates are a set of conditions long accepted as the requirements for establishing a fixed microorganism as the cause of a specific disease. The case for HIV as the AIDS virus or COVID – 19 causes acute lung disease syndrome (ARDS) as with the identification of any so-called causative infectious agent, should depend upon meeting these parameters, of which there are four. (Keep in mind that researchers disagree about what constitutes proof that any germ causes a disease.)

1. The germ must be found in all cases of the disease.

Tissues said to be affected by HIV or COVID -19 include primarily the white blood cells of the immune system, particularly the T-cells, the brain neurons in dementia, skin cells in lesions of Kaposi’s sarcoma, in the lungs as well as, theoretically, any cell in the body expressing the CD4 surface receptor said to be the key to HIV or COVID – 19 cell entry. But no trace of the virus can be found in either the Kaposi’s sarcoma or the neurons of the central nervous system or the lungs in Acute Respiratory Disease Syndrome or ARDS. HIV and COVID -19 have moved from involving only immune cells to other types of cells in order to explain certain AIDS-defining symptoms or COVID -19 defining symptoms which are not immune deficiencies anyway, including the cancers, dementia and wasting diseases, dry cough, fevers and hypoxia which have not been, or cannot be, explained in terms of a germ-theory virus model that involves destruction of the immune system.

And, if HIV or the COVID-19 viruses were actively infecting T-cells or other members of the body’s immune system, extracellular virions should easily be found circulating in the blood. But in most individuals suffering from AIDSyndrome or COVID – 19, no particles can be found anywhere in the body.

Another aspect of HIV is that now several HIV and COVID “reservoirs” have been suggested. One encyclopedia, which will go unnamed, says: “Researchers have also been able to show direct infection of bone-marrow cells-the precursors of circulating blood cells-and the proliferation of the virus within these cells. Thus bone marrow may represent an important reservoir of HIV or in COVID -19 the interstitial fluids of the Interstitium in an infected person and provide a potential mechanism for dissemination of the virus through the body.” This is misinformation, pure speculation, a conclusion based on laboratory pyrotechnics, or scientific fraud. It is also said that macrophages can support HIV and COVID-19 replication while harboring the virus from immune surveillance. Circulating macrophages are said to play an important role in the distribution of HIV and COVID-19 throughout the body, including the lung and brain. The question is, wouldn’t there be significant amounts of virus in a reservoir? The fact remains: it is nearly impossible to recover HIV or COVID – 19 from its “victims.” (See below under “Autoimmune Theory.”) One paper published in March 1993 reported two individuals with about 100,000 particles per milliliter of blood, among dozens of patients with little or no detectable extracellular particles [18].

The abundance of uninfected T-cells (about one in 500) in all patients is the definitive argument against the false claims for high cell-wall particle “loads,” or “burdens”. The absence of active, infectious virus automatically disqualifies HIV as a player in the AID Syndrome or COVID – 19 in acute lung disease syndrome (ARDS).

2. The germ must be isolated from the host and grown in pure culture.

Even for the most experienced virus hunters, a virus that is so extremely scarce is difficult to find. Only with rare luck and extreme persistence has HIV or COVID – 19 been extracted from an antibody-positive person. This amounts to finding the proverbial needle of HIV or COVID – 19 in a haystack of human DNA. This difficulty speaks to HIV’s or COVID – 19’s lack of potential in disease.

3. The purified germ must cause the disease again in another host.

There is no animal or human model for HIV and AIDS or COVID – 19 and ARDS, and where there is no animal or human model, you cannot establish Koch’s postulates. (It is more than disconcerting to think of the number of primates that have been injected to this day in an attempt to produce AIDS.) HIV jumps in and says that HIV or any virus including COVD – 19 should receive special dispensation from Koch’s postulates. A major stumbling block is the latency which is claimed, but whose modus is not explained by authorities. In 1989 the official latent period between HIV infection and the onset of AIDS was one year. This period of “incubation” has since been stretched to 10 to 12 years. For each year that passes without the predicted explosion in AIDS cases, approximately one year is added to this period. Even this is insufficient; with only 5 percent of do-called infected Americans developing AIDS each year, the average latent period would have to be revised to more than 20 years for 100 percent to become sick.

HIV should cause AIDS and COVID – 19 should cause ARDS within two weeks of infection at most, but it does not, and with the complete lack of a demonstrated process by which HIV or COVID – 19 diminishes immune function, belief in a decade or more of unexplained latency requires a level of “faith” beyond my capacity. Another major stumbling block is that even once the latent period of 14 days is apparently over, there is still precious little development of the HIV or COVID – 19 virus.

4. The germ must then be isolable from the newly infected host.

A huge problem for the viral theory! We are now backing to the problem of meeting requirement number 2.

The Antibody That Isn’t an Antibody

According to the germ theory, an antibody is a certain antidote to a pathogen or virus. According to HIV and COVID -19, however, the more antibodies you have to HIV or COVID – 19, the sicker you are said to be. Viruses, including HIV and COVID – 19 are two of thousands “disease causing agents” in the allopathic file cabinet in which antibodies to the causative agent mean you’re in trouble; and it defies just about every known law, rule, guideline, fact, and behavior in the germ theory book. This includes, as we have seen in Koch’s postulates, and, as we will see below, Farr’s Law.

Furthermore, vaccine research proceeds on the basis of producing antibodies from a phantom virus in the patient. Apparently, these “synthetic” antibodies delivered in a vaccine with GMO organisms mixed with toxic metals and chemicals such as aluminum oxide, will signal recovery, while one’s own natural ly created antibodies signals death.

The Autoimmune Theory

One explanation put forth for the deadliness of such a scarce pathogen is that it somehow induces a self-destructive immune response (the system attacks itself). Evidence for this is said to be low white cell counts in people with infections; however, there is nothing to support the hypothesis, i.e., no plausible process by which this occurs has been suggested.

I have never viewed under a pHase contrast microscope a white blood cell attack another white blood cell in my 40 years of research watching and video taping their activities. White blood cells are glorified janitors or garbage collectors going around the body fluids picking up cellular fragments and biological transformations, i.e., bacteria and yeast. But they never attack each other or a healthy blood or body cell.

Watch the following video of two neutrophils moving around through the blood plasma while cleaning the membranes of red blood cells and picking up small bacteria and Y-form yeast. In fact, you will see one of the neutrophils picking up a Y-form yeast, like Candida albicans and then spitting it back out into the blod plasma.

The Elastic Band Theory

For the sake of discussion, let us allow germ-theory interpretation of immune function and autoimmunity. With only one in 500 immune cells (white blood cells) said to be infected with COVID -19 positives, it would seem to require a virus of extraordinary cunning to get uninfected cells to attack each other and not infected ones, which would be self-defeating for the virus. Or in the latter event, such cunning could be matched only by the adroitness required to move quickly from one host cell to another just before destruction. Or, if macrophages are involved, the process should lead either to increasing titers of virions in the blood, lymph, etc., as infected cells are lysed, or to increasing concentrations in macrophages if they are ingesting T-cells. This supports the reservoir notion (if there were any viruses to be found in them). It is thus easier to expand the theory to an ELASTIC BAND THEORY to meet whatever the outcomes are of the virologist for any virus, including HIV and COVID – 19! How about fourteen day latency period. Maybe a 2 year or even with HIV a 20 year latency period. Really! This is called science!

(Please read for further light and knowledge on viruses at: “Dismantling the Viral Theory” at: https://www.drrobertyoung.com/post/dismantling-the-viral-theory

COVID – 19 and Farr’s Law

Established in the early 1900s, Farr’s Law, which is fundamental to virology, states that viral disease develops exponentially, and dictates that illness will strike soon after infection. The rate-determining factor of the exponential growth of viruses is viral generation time, which is between 8 and 48 hours. Since laws are made to be broken or excepted, viruses with incubation periods longer than allowed by Farr’s Law are called “slow viruses.” And since COVID – 19 joins an exonerated class of viruses by not multiplying according to this law of virology, virologists stretch the time to accommodate it. The question arises, though, of how anyone can determine or demonstrate when a “natural” COVID -19 infection takes place, and thus determine latency, since no one is being tested daily or weekly, etc., and there is no animal model. Within the slow-virus concept, adopted as an exception to Farr’s Law, retro virologists can find refuge, hold on to their theory, hibernate in their labs, and hope the long winter of HIV latency is over before they expire.

According to expert retro virologist Dr. Peter Duesberg, “The slow virus concept has never been reconciled with the short generation time of viruses and the immune system. Once the virus lies totally dormant, an intact immune system will never allow any virus to be reactivated to multiply into numbers that would threaten the host. For a virus to be reactivated, the immune system first must be destroyed by something else-the real cause of a disease. A reactivated virus would just contribute an opportunistic infection. Thus, there are no slow viruses, only slow virologists.” [19] Also, says Duesberg, “Retroviruses are all very similar. I mean, there are differences, but as far as pathology is concerned, you don’t see a marker in one which is going to explain why it supposedly wakes up from sleep and becomes active” [20].

As of April 22nd, 2020, I have yet to see ANY published research papers identifying the existence of a single virus that has proven out to cause ANY specific disease(s) following the scientific method. It appears that virologists have given the virus a pass because they JUST CANNOT FIND ONE!

The use of PCR testing, is one of the main tests being used by virologists today to determine antibody loads for the corona virus. It is very important for you to know that the PCR testing does not identify the existence of ANY specific virus. So, what you get is a guess. This is NOT science!

The following is another important quote concerning viruses, specifically HIV and AIDS from Dr. Mullis, “we have not been able to discover any good reason why most of the people on earth believe that AIDS is …caused by..HIV. There is simply no scientific evidence demonstrating that this is true (or) why doctors prescribe a toxic drug called AZT…we cannot understand why humans would take that drug for any reason.”

The AZT drug was one of the first drugs given for the treatment of HIV even when the patient was asymptomatic. Sadly, this toxic acidic drug was the cause of the AIDS and the death of millions. Not some illusionary virus. AZT is no longer being used because of this fact.

Third, read Robert O Young, MSc, DSc, PhD, Naturopathic Practitioner book, “A Second Thought About Viruses, Vaccines and the HIV/AIDS Hypothesis.”

This book also covers additional information on other phantom viruses such as the Ebola virus, West Nile virus, and the Hepatitis virus, just to name a few.

The link to purchase this book is:

Second Thoughts about Viruses, Vaccines, and the HIV/AIDS – Booklet

Fourth, watch the following youtube video of Dr. Thomas Cowan, MD, on the , “Relation between Corona virus, Electromagnetic waves, 5G, Vaccines and even Spirituality” on the cause and symptoms of the phantom Corona virus.

Now Let’s look at the 5G viral map of Canada, USA, Mexico, Central America and Northern South America at: https://www.speedtest.net/ookla-5g-map and see where the deployment of 5G viral cell towers are located and the hot spots for so-called COVID – 19 infections and deaths.

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Please note that New York and New Jersey have the greatest number of 5G viral cell towers with 1.5K and the greatest number of sick and dead. The second greatest number of 5G viral cell towers with 430 are found in the Los Angeles, California area with the second highest number of sick and dead. It does not take a rocket scientist to figure out the cause and effect relationship between radiation poisoning with the symptoms of dry cough, hypoxia, and fever when you understand and know that 5G pulsating V-frequency at 60GHz literally takes the oxygen out of the air and out of your body destroying the red blood cells and their ability to flow to the lungs and pick up oxygen and then flow back to deliver this life-needing oxygen to the body cells. All of the symptoms for 5G viral radiation poisoning are identical to high-altitude sickness. You cannot treat these symptoms like the season flu or Influenza or you will kill the patient.

Fifth, watch Dr. Judy Mikovits PhD (American Researcher) on Coronavirus on the HIV to the Corona virus fraud and her 22 year relationship with Dr. Anthony Fauci, the director of the National Institute of Allergy and Infectious Diseases –

Sixth, Watch from the NYC ICU: DOES COVID-19 REALLY CAUSE ARDS or Acute Respiratory Disease Syndrome??!!

Seventh, watch ‘Corona Virus’ & 5G – What Is A Virus? Dr. Robert O. Young. Here is the link:

https://www.bitchute.com/video/jqD5tbQO1WUT/?fbclid=IwAR1BUXHvCPRd7lXpCvu3_tKqbrMA12-FAKImabX1-Vlo0rUayvqRAu3DsDc

The following micrographs, using pHase contrast microscopy that I observe in healthy red blood cells that are oxygen-rich and the second micrograph is of unhealthy red blood cells that are oxygen-deprived indicated by the white target or missing red blood cell hemoglobin. You can also see the degeneration of the cell membranes with spiking or knobs indicating the ‘corona effect’, a symptom caused by an acidic lifestyle and radiation poisoning.

Micrograph of Healthy Oxygenated Red Blood Cells

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References

  1. Hodgkinson N (1992) Experts Mount Startling Challenge to AIDS Orthodoxy. Sunday Times, London.

  2. Carroll, John (1993) The Weird Way to Win a Nobel Prize. San Francisco Chronicle, E9.

  3. Mirvish SS, Williamson J, Badcook D, Chen SC (1993) Mutagenicity of Iso-butyl nitrite vapor in the Ames test and some relevant chemical properties, including the reaction of iso-butyl nitrite with phosphate. Environ Mol Mutagen 21(3): 247-252.

  4. Rappaport John (1988) AIDS Inc., Scandal of the Century. Human Energy Press, California, USA, p. 38.

  5. Ibid p. 40.

  6. Fungalbionics Convention (1994) The Fungal/Mycotoxin Etiology of Chronic and Degenerative Disease. Metro Toronto Convention Centre, USA.

  7. Konotey-Ahulu (1989) F.I.D. What is AIDS? Watford England: Tetteh-A’Domeno Co., UK, pp. 109.

  8. Rappaport op. cit. p. 73.

  9. Williams AO (1992) AIDS: An African Perspective. Boca Raton, Fla.: CRC Press, pp. 238.

  10. Duesberg PH Inventing the AIDS t7ras, pp. 293.

  11. Konotey-Ahulu op. cit., p. 56-57.

  12. WHO (1995) The Current Global Situation of the HIV/AIDS Pandemic. World Health Organization, Switzerland.

  13. Duesberg PH (1992) AIDS acquired by drug consumption and other non contagious risk factors. Pharmacol Ther 55(3): 201-277.

  14. Ibid p. 240.

  15. Rappaport, op. cit., p. 71-82.

  16. Biggar RJ, Melbye M, Kestens L, de Feyter M, Saxinger C, et al. (1985) Seroepidemiology of HTLV-III antibodies in a remote population of Eastern Zaire. Br Med J 290: 808-810.

  17. Duesberg PH (1987) Retroviruses as carcinogens and pathogens: Expectations and reality. Cancer Research 47: 1199-1220.

  18. Lemonick MD (1995) Return to the Hot Zone. Time International.

  19. Duesberg PH, AIDS acquired by drug consumption. pp. 237-238.

  20. Rappaport, op. cit., p. 130.

  21. Culbert, Michael L (1898) Committee on Government Operations AIDS Drugs: Where Are They? 73rd Report. AsIDS: Hope Hoax and Hoopla, The Bradford Foundation, Chula Vista, Cal, p. 10-11.

  22. Chiu D, Duesberg PH (1995) The toxicity of Azidothymidine (AZT) on human and animal cells in culture at concentrations used for antiviral therapy. Genetica 95: 103-109.

  23. Duesberg PH, AIDS acquired by drug consumption. pp. 201-277.

  24. Yarchoan R, Pluda JM, Perno CF, Mitsuya H, Broder S (1991) Anti-retroviral therapy of human immunodeficiency virus infection: Current strategies and challenges for the future. Blood 78(4): 859-884.

  25. McLeod GX, Hammer SM (1992) Zidovudine: Five years later. Ann Intern Med 117(6): 487-501.

  26. Duesberg PH (1995) Is HIV the cause of AIDS? Lancet 346(8986): 1371-1372.

  27. Coulter Harris L (1987) AIDS and Syphilis- The Hidden Link. Berkeley, California, USA, p. 37.

  28. Rappaport, op. cit., pp. 152-153.

  29. James, Walene (1995) Immunization: The Reality Behind the Myth. (2nd edn), Bergin & Garvey (Eds.), Greenwood Publishing Group, Westport, CT, p. 35-36.

  30. Sermos Gus G (1988) Doctors of Deceit and the AIDS Epidemic-An expose of the Centers for Disease Control by an insider. GGS Publishing, USA, p. 3.

  31. RO Young (1999) Sick and Tired. Woodland Publishing, USA.

Do Germs Like the CoronaVirus Cause Disease?

Is it the Germ that Causes a Sickness or Disease or a Toxic Acidic Environment?

Human beings, the potentially highest form of life expression on this planet have built the vast pharmaceutical industry for the central purpose of poisoning the lowest form of life on the planet–germs! One of the biggest tragedies of human civilization is the precedence of chemicals over nutrition.”–Dr. Richard Murray

“In the sciences, people quickly come to regard as their own personal property that which they have learned and had passed on to them at the universities and academies. If someone else comes along with new ideas that contradict the Credo and in fact even threaten to overturn it, then all passions are raised against this threat and no method is left untried to suppress it. People resist it in every way possible: pretending not to have heard about it; speaking disparagingly of it, as if it were not even worth the effort of looking into the matter. And so a new truth can have a long wait before finally being accepted.”–Goethe

Misconceptions about health are ingrained in our culture. The road to understanding the process of maintaining and restoring health has been a long and twisted one. From ancient and intuitive knowledge, science has taken over, made colossal errors, and clings to them for dear life. There was a rejection of wisdom or scientific discovery in favor of a more popular, convenient, or politically desirable system. Just as Socrates was poisoned for his ideas, and Galileo was forced by a fanatic clergy to withdraw his statements about astronomy, ignorance and power can be a dangerous combination.

We do not catch diseases. We build them with what we have to eat, drink, think, breathe, feel and believe them into existence. We work hard at developing our diseases. We must work just as hard at restoring health. The presence of germs (virus, bacteria, yeast or mold and their associated exotoxins, endotoxins and mycotoxins – acids) does not constitute the presence of a sickness or disease. Bacteria are scavengers of nature…they reduce dead tissue to its smallest element. Germs or bacteria have no influence, whatsoever, on live cells. Germs or microzymas flourish as scavengers at the site of disease. They are just living on the unprocessed metabolic waste and diseased, malnourished, nonresistant tissue in the first place. They are not the cause of the disease, any more than flies and maggots cause garbage. Flies, maggots, and rats do not cause garbage but rather feed on it. Mosquitoes do not cause a pond to become stagnant! You always see firemen at burning buildings, but that doesn’t mean they caused the fire…

Pasteur vs. BeChamp – Monomorphism or Pleomorphism

Traditional Western medicine teaches and practices the doctrines of French chemist Louis Pasteur (1822-1895). Pasteur’s main theory is known as the Germ Theory of Disease. It claims that fixed species of microorganisms or microbes (virus, bacteria, yeast or mold) from an external source invade the body and are the first cause of infectious disease. The concept of specific, unchanging types of microbes causing specific diseases became officially accepted as the foundation of allopathic Western medicine and microbiology in late 19th century Europe. Also called monomorphism,(one-form), it was adopted by America’s medical/industrial complex, which began to take shape near the turn of the century. This cartel became organized around the American Medical Association, formed by drug interests for the purpose of manipulating the legal system to destroy the homeopathic medical profession.

Controlled by pharmaceutical companies, the complex has become a trillion-dollar-a-year business. It also includes many insurance companies, the Food and Drug Administration (FDA), the National Institutes of Health (NIH), the Centers for Disease Control (CDC), hospitals, and university research facilities from around the World. The microbe doctrine gave birth to the technique of vaccination that was blindly begun in 1796 by Edward Jenner. Jenner took pus from the running sores of sick cows and injected it into the blood of his “patients.” Thus was born a vile practice (immunization/vaccination) whose nature has changed little to this day, and whose understanding is still clouded by Pasteur’s germ theory. This also gave birth to the development of antibiotics (against life), the first being penicillin in 1940. An antibiotic is the poisonous acidic waste from a fermenting cell used in the attempt to kill another microbe. Penicillin is the urine from a fungus called Penicillium when it ferments sugar giving rise to a highly acidic waste. In other words ALL antibiotics and chemicals in vaccines are highly acidic urine like metabolic waste that will and does compromise the delicate pH balance of our body fluids, especially the interstitial fluids of the Interstitium organ compartments or holding tanks.

So what is the big deal about phantom viruses, like HIV, Hepatitis C, Ebola, SARS, West Nile, Zika, Measles, Polio or even Corona Virus when we know that a viruses are nothing more than the biological acidic waste (urine and feces) from cellular transformations due to a declining alkaline pH that gives rise to different microbial forms such as bacteria, yeast, and mold and their acidic wastes. The ability of matter to change its form and function is know as pleomorphism (many forms) and was introduced by Antione BeChamp, a French Medical Doctor and research scientist who discovered that bacteria is born in us and from us.

A Double Whammy

Bottom-line, it is all about the environment folks and has very little to do with the microbe or germ except if germs and their acidic waste products are present in the body this is the evidence of a polluted/acidic internal terrain or environment caused directly by what one eats, what one drinks, what one breathes, what one thinks, what one feels and what one believes!

The Germ is Nothing!

The germ is nothing and the environment is everything. The Corona Virus, the cancer, the heart condition, the diabetes is nothing more than unhealthy body cells biologically transforming/ mutating to unhealthy body cells as a result of being poisoned by their toxic/acidic environment from ones acidic lifestyle and dietary choices.

 

Yes, disease is manufactured by YOU and your own acidic choices from what you eat, what you drink, what you breathe, what you think, what you feel and what you believe. Disease is not something that you get or catch it is something YOU do.

So STOP believing in a phantom virus (HIV, Hepatitis C, Ebola, West Nile, Flu, SARS, ZIKA, Measles, Polio or CORONA VIRUSES) and the germ theory (which has never been proven to cause any disease) and realize that you are the author of your health and fitness or the author of your sickness and disease. Choices do have consequences! And, Ignorance is NO excuse!

How do I know this?

Because as an internal environmentalist, biochemist, naturopathic practitioner and expert in nutrition, I test the chemistry, including the pH, of all the body fluids. This includes the intravascular fluids, the interstitial fluids of the Interstitium compartments, the intracellular fluids, the transintracellular fluids and how these fluids effect the health of every organ, gland and tissue. The Test is called the L.I.F.E. Test which is an acronym which stands for, “Living Interstitial Fluid Environment.(TM)

Conclusion

Finally, the genesis/origin of ALL sickness and disease begins in the interstitial fluids of the Interstitium compartments that hold the acidic metabolic waste of all cellular functions until it can be released via the lymphatic system through the four channels of elimination – urination, respiration, defecation or perspiration!

There is NO DOUBT in my mind and millions of others around the World that viruses (acidic toxic waste chemicals), bacteria, yeast, fungi and molds are NOTHING more than the evidence of cellular breakdown due to a toxic acidic environment created by individual choice!

The solution at the beginning of any acidic symptomology is very simple – take the alkalizing salts including puripHy drops, pHlavor salts and pHour salts and experience your acidic caused symptoms of sickness and disease disappear in just a few days as you begin to alkalize your body fluids back to their alkaline designed pH of 7.365!

To order these products go to: http://www.phmiracleproducts.com

So get off your acid and go to health with an alkalarian lifestyle and diet as outlined in the pH Miracle books and soon to be released, Thrive On Perfect Health (pH) – L.I.F.E. – Living Interstitial Fluids – www.drrobertyoung.com

Remember this important understanding about germs and the environment, “The germ is nothing the terrain is everything” Claude Bernard

Has the Existence of Polio, Measles, HIV, CMV, EBV, Hep C, Ebola, the Flu, and Now Zika Viruses Been Demonstrated and Scientifically Proven?

Dismantling The Viral Theory

[Electron micrograph of the so-called Polio virus that has never been demonstrated scientifically to cause the symptoms of paralysis.  Illustration has been colorized for effect]

The first isolation of a virus was achieved in 1892 by Russian bacteria hunter Dimitri Iwanowski, who gathered fluid from diseased tobacco plants. He passed this liquid through a filter fine enough to retain bacteria; yet to Iwanowski’s surprise, the bacteria-free filtrate easily made healthy plants sick. In 1898 a Dutch botanist, Martinus Willem Beijerinck, repeating the experiment, also recognized that there was an invisible cause and named the infectious agent “tobacco mosaic virus.” In the same year as Beijerinck’s report, two German scientists purified a liquid containing filterable viruses that caused foot-and-mouth disease in cattle (viruses were at one time called “filterable viruses,” but eventually the term “filterable” came to apply only to viruses, and was dropped). Walter Reed followed in 1901 with a filtrate responsible for yellow fever, and soon dozens of other disease-causing viruses were found.

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In 1935 another American, Wendell M. Stanley, went back to the beginning and created pure crystals of tobacco mosaic virus from a filtered liquid solution. He affirmed that these crystals could easily infect plants, and concluded that a virus was not a living organism, since it could be crystallized like salt and yet remained infectious. Subsequently, bacteriologists all over the world began filtering for viruses, and a new area of biology was born-virology.

Historically, medical science has vacillated on the question of whether a virus is alive. Originally it was described as nonliving, but is currently said to be an extremely complex molecule or an extremely simple microorganism, and is usually referred to as a parasite having a cycle of life. (The term “killed” is applied to certain viral vaccines, thus implying an official conviction that viruses live.) Commonly composed of either DNA or RNA cores with protein coverings, and having no inherent reproductive ability, viruses depend upon the host for replication. They must utilize the nucleic acids of living cells they infect to reproduce their proteins (i.e., trick the host into producing them), which are then assembled into new viruses like cars on an assembly line. Theoretically, this is their only means of surviving and infecting new cells or hosts.

The Replicating Virus Theory

Then it was discovered that, when bacteria slowly begin to die, bacteria create tiny, apparently lifeless forms of survival, the so-called spores. It was then suspected that these spores were toxic and that they were the so-called pathogenic poisons. This was then refuted, since the spores are rapidly developing into bacteria when their vital resources are being restored. When scientists in the laboratory observed that the weak, highly inbred bacteria perished very quickly while turning into much smaller structures than the spores, it was first believed that the bacteria were being killed by the alleged pathogenic poisons, called viruses, and that the viruses were thereby replicating.

[The micrograph above was done using Dark Field Microscopy showing red blood cells and the evolution of bacterial pHages and bacterial spores (the white spots0 from red blood cell biological transformation]

The Replicating Virus Theory

Then it was discovered that, when bacteria slowly begin to die, bacteria create tiny, apparently lifeless forms of survival, the so-called spores. It was then suspected that these spores were toxic and that they were the so-called pathogenic poisons. This was then refuted, since the spores are rapidly developing into bacteria when their vital resources are being restored. When scientists in the laboratory observed that the weak, highly inbred bacteria perished very quickly while turning into much smaller structures than the spores, it was first believed that the bacteria were being killed by the alleged pathogenic poisons, called viruses, and that the viruses were thereby replicating.

The Invention of Bacterial Viruses

Due to the belief that these – at the time of their discovery still invisible- structures were killing the bacteria, they were called phages/bacteriophages, “eaters of bacteria”. Only later it was determined that merely highly inbred and therefore almost non-viable bacteria can be made to turn into phages, or bacteria which are being destroyed so fast that they do not have time to form spores.

The introduction of the electron microscopy led to the discovery of the structures resulting from the biological transformation or pleomorphism of bacteria when these were suddenly dying or when the metabolism of the highly inbred germs was overwhelmed by processes triggered by the adding of “phages”. It was also discovered that there are hundreds of types of different-looking “phages”. The discovery of phages, the so-called bacterial “viruses”, reinforced the wrong assumption and the belief that there were human and animal viruses that looked the same and had the same structure. This is not and cannot be the case, for several different reasons.

After introducing chemical examination techniques in biology, it was discovered that there are thousands of types of phages and that phages of one type always have the same structure. They consist of a particular molecule, made of nucleic acid, which is covered in a shell of proteins of a given number and composition. It was only later discovered that merely the bacteria which had been highly inbred in the test tube could turn into phages themselves, by contact with phages, but this never applied to natural bacteria or bacteria which had just been isolated from their natural environment. In this process, it was discovered that these “bacterial viruses” actually serve to provide other bacteria with important molecules and proteins, and that the bacteria themselves emerged from such structures.

Before it could be established that the “bacterial viruses” cannot kill natural bacteria, but they are instead helping them to live and that bacteria themselves emerge from such structures, these “phages” were already used as models for the alleged human and animal viruses. It was assumed that the human and animal viruses looked like the “phages”, were allegedly killing cells and thereby causing diseases, while at the same time producing new disease poisons and in this way transmitting the diseases. To date, many new or apparently new diseases have been attributed to viruses if their origin is unknown or not acknowledged. This reflex found an apparent confirmation in the discovery of the “bacterial viruses”.

It is important to note that the theories of fight and infection were accepted and highly praised by a majority of the specialists only if and when the countries or regions where they lived were also suffering from war and adversity. In times of peace, other concepts dominated the world of science.[272]

It is very important to note that the theory of infection – starting from Germany – has only been globalized through the third Reich, when the Jewish researchers, most of which had opposed and refuted the politically exploited theories of infection, were removed from their positions.[273]

The Detection of Phages and Biological Transformation

The existence of phages can be proved rapidly

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[Bacterial pHage being born out of a blood and/or body cell.  A biological process known as pleomorphism]

First step: their presence is confirmed through an effect, namely the transformation of bacteria into phages, and also through an electron micrograph of those phages. The control experiments show that phages do not appear if bacteria do not change or if bacteria randomly start decomposing due to extrinsic sudden annihilation, without forming phages.

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[The micrographs (micrographs #1 through #6] above show the cellular transformation of red blood cells, using pHase contrast microscopy, into rod bacteria, cell-wall deficient bacteria, Y-form yeast and then bacteria pHages]

Second step: the liquid containing the phages is concentrated and applied on another liquid, which has a high concentration at the bottom of the test tube and a low concentration at the top of the test tube. The test tube with the phages is then powerfully spun (centrifuged) and all the particles gather according to their mass and weight to the place of their own density. The density is the ratio of weight (mass) per unit of volume, expressed as Kg/l or g/mg, respectively. That is why this concentration and purification step for particles with the same density is called density gradient centrifugation.

The layer where many particles of the same density gather becomes “cloudy”, which is called a “band.” This step is being documented, then the particles concentrated, purified and sedimented in a “band” are removed with a syringe needle. The extracted concentrated amount of particles is called an isolate. A fast and simple electron micrograph will confirm the presence of phages in the isolate, which at the same time is an indication for the purity of the isolate, if the micrograph shows no other particles but the phages. The appearance and the diameter of the phages will also be established with the help of this micrograph.

The control experiment performed for this step consists in treating and centrifuging the liquid from bacteria which did not form any phages, where no phages appear at the end of the procedure.

After the step of successfully isolating the phages, the decisive biochemical characterization of the phages follows. The biochemical characterization of their composition is essential for identifying the specific type of phage, since different types of phages often appear to be similar. The isolate obtained through the density gradient centrifugation is now divided in two parts. One part is used to determine the size, type and composition of the nucleic acid; in a separate procedure, the other part is used to determine the amount, size and morphology of the proteins of the phages. Since the 1970s, these tests have been simple standard techniques that are learned by every biology student in their first semesters.

These tests represent the biochemical characterization of the phages. In almost every case, these results have been and are being published in only one publication, since a phage has a very simple structure which is very easy to analyze. The control experiments for these tests use liquid from bacteria which do not form phages and thus cannot present any biochemical proof. The existence of approximately two thousand different types of phages have been scientifically demonstrated this way

The So-Called Pathogenic Viruses

The “bacteriophages,” correctly defined as incomplete mini spores and building blocks of the bacteria, have been scientifically isolated, while the so-called pathogenic viruses have never been observed in humans or animals or in their body fluids and have never been isolated and subsequently biochemically analyzed. To date, none of the researchers involved in virology research seems to have realized this very important point.

The use of electron microscopy and the biochemistry were very slowly returning to normal after 1945 and no one had realized that not one pathogenic virus had ever been isolated in humans or animals; thus, as of 1949 researchers started applying the same idea used for the (bacterio) phages, in order to replicate the human and animal “viruses.” John Franklin Enders, born in 1897 in the family of a rich financier, was active in various fraternities after having finished his studies, then he worked as a real estate agent and studied foreign languages for four years before turning to bacterial virology, which fascinated him. He then simply transferred the ideas and concepts that he learned in this area of research to the supposed pathogenic viruses in humans.

UnScientific Experiments and Interpretations Gave Birth to Virology

With his unscientific experiments and interpretations that he had never confirmed through negative controls, Enders brought the entire “viral” infectious medicine to a dead end. It is important to note at this point that Enders, like many infectious diseases specialists, worked for the U.S. military, which had always been and remains to date a huge victim of the fear of contagions. It was mainly the U.S. military which spread its erroneous belief that besides chemical weapons there were also biological weapons in the form of bacteria and viruses.

In 1949, Enders announced that he had managed to cultivate and grow the alleged polio virus in vitro on various tissues. The American expert opinion believed everything immediately. What Enders did was to add fluids from patients with poliomyelitis to tissue cultures which he claimed to have had sterilized, then he alleged that the cells were dying because of the virus, that the virus was replicating in this way and that a vaccine could be harvested from the respective culture. At that time, summer polio epidemics (polio = flaccid paralysis) were very frequent during summer and they were believed to be caused by the polio virus. A vaccine was to help eradicate the alleged virus. After the polio vaccine was introduced, the symptoms were then re-diagnosed among other things as multiple sclerosis, flaccid acute paralysis, aseptic meningitis etc. and later polio was claimed to have been eradicated. During his experiments, Enders et al. sterilized the tissue cultures in order to exclude the possibility of bacteria killing the cells. What he didn’t take into consideration was that the sterilization and the treatment of the cell culture when preparing it for the alleged infection was exactly what was destroying and killing the cells. Instead, he interpreted the cytopathic effects as the existence and the action of a so-called polio virus, without ever having isolated a single virus and describing its biochemistry. The necessary negative control experiments, which would have shown that the sterilization and the treatment of the cells prior to the “infection” in the test tube was killing the cells, have never been performed. However, for this “performance” Enders received the Nobel prize in 1954.

The Invention of the Polio Virus and ‘YES” the Measles Virus Too!

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[Measles virus or a bacterial pHage?]

1954 is also the year in which Enders applied and introduced the same technique in order to allegedly replicate the measles virus. As he had been awarded the Nobel prize for the alleged polio virus the same year, all researchers believed his technique to be scientifically valid. Thus, to date, the entire concept of polio and measles has been based upon this unscientific technique and fraud.

Thus, the polio and measles vaccines do not contain viruses, but particles of dead monkey kidney tissue or human cancerous body cells. To date, no negative control experiments have been done with respect to the so-called polio and measles viruses either, which would have shown that it was the laboratory procedures that lead to the cytopathic effects on the cells.

Additionally, all claims and experiments made by Enders et al. and subsequent researchers lead to the only objective conclusion, that in fact they were observing and analyzing the cellular particles or fragments and the activity thereof in the test tube, misinterpreting these as particles and characteristics of the alleged polio and/or measles viruses.

ALL Viruses from HIV, EBV, CMV, Hepatitis C, West Nile Virus, Ebola, Measles, Zika, etc., are ALL Phantom Viruses

Viral Existence Has NEVER Been Scientifically Demonstrated and Never Proven!

The following explanations applies to all the so-called (human or animal) “pathogenic viruses”. The six papers provided by Dr. Bardens in the course of the “measles trial” as proof for the existence of the measles virus described in a didactically ideal way the various steps of the chain of misinterpretations up to the belief in the existence of a measles virus.

The first paper was published in 1954 by Enders et al.: “Propagation in tissue cultures of cytopathogenic agents from patients with measles” (Proc Soc Exp Biol Med. 1954 Jun; 86 (2): 277–286).

This publication can be found on the internet, like all the other publications presented at the measles trial. In that experiment, Enders et al. cut down dramatically on the nutrient solution and added cell-destroying antibiotics to the cell culture before introducing the allegedly infected fluid. The subsequent dying of the cells was then misinterpreted as presence and also isolation of the measles virus. No control experiments were performed to exclude the possibility that it was the deprivation of nutrients as well as the antibiotics which led to the cytopathic effects.

Enders’ and his colleagues’ blindness can be explained by the fact that he truly wanted to help people, while the ‘virus hysteria’ was intensifying after the war and during the cold war. It can also be explained by the fact that Enders and many of his colleagues had no idea about medicine or biochemistry and they were competing with the Soviet Union for the development of the first measles vaccine. Such a pressure for success can also explain why Enders and his colleagues ignored their own reservations and cautions expressed in 1954, when they had observed and noted that many cells also died after being treated normally (i.e. without being “infected”), which they thought to have been caused by unknown viruses and other factors.  All these facts and cautions were subsequently disregarded.

The second paper presented by the claimant in the ‘measles trial’ was published in 1959[274] and, for the reasons presented above, the authors concluded that the technique introduced by Enders was not appropriate for the isolation of ANY virus. This rebuttal is not only NOT being discussed by ALL the other researchers, but it is being ignored completely!

The ‘Viral Dogma’ of Pathogenic Viruses is Still Being Promoted Today!

In a third paper[275], the authors photographed typical cellular particles inside the cells and misinterpreted these as measles virus. They did not isolate any virus. For unexplained reasons, they failed to determine and describe the biochemical structure of what they were presenting as a virus in a separate experiment. In the short description of the methods used, one can read that the authors did not apply the standard isolation technique for viruses, i.e. the density gradient centrifugation. They simply centrifuged fragments of dead cells at the bottom of a test tube and then, without describing their biochemical structure, they misinterpreted the cellular debris as viruses.

From the way the experiments were performed, one can only conclude that cellular particles were misinterpreted as viruses. We find the same situation in the fourth[276] and the sixth[277] publication put forward by the claimant as proof of the existence of a measles virus. The fifth publication[278] is a review describing the consensus process as to which nucleic acid molecules from the dead cells would represent the so-called genome of the polio or measles virus. The result is that dozens of research teams work with short pieces of cell-specific molecules, after which -following a given model – they put all the pieces together on paper. However, this jigsaw puzzle made of so many pieces was never scientifically proven to exist as a whole and was never isolated from a virus, for a polio, measles, HIV or Hepatitis C, Ebola or Zika viruses have never been seen, neither in humans nor in a test tube. Referring to this publication, the court-appointed expert stated that it described the gold standard, i.e. the entire virus genome. It is obvious that the expert did not read this paper, whose authors stated that the exact molecular composition and functions of the measles virus genome will have to be the object of further research, which is why they had to rely on other virus models in order to achieve a consensus on the structure and functions of ANY virus genome. The easiest thing for anyone to notice is that in all of these publications, as well as in all other publications on the “measles virus” and other pathogenic viruses, including HIV, EBV, CMV, Ebola and Zika, no control experiments have ever been performed. No researchers used the density gradient centrifugation technique; instead, they only centrifuged cellular debris at the bottom of a test tube. This technique, used to collect all the particles from a fluid, is called pelletizing. From a logical and scientific perspective, it can be said that in all publications on the so-called “pathogenic viruses”, the researchers demonstrated in fact only particles and characteristics of cells. I would also like to point out that the so-called giant viruses[279] , i.e. an enwrapped nucleic acid can be found everywhere in the sea and in basic organisms. Like all bacterial phages, not only are they harmless, but they have beneficial functions. They can be also isolated by using the density gradient centrifugation, which proves their existence (see the graphic above).

I also recommend Prof. Lüdtke’s relevant review (1999).[280] He noted that at the early beginnings of virology, the majority of virologists always concluded that the structures they had mistaken for viruses turned out to be components of the cells and thus, they were only the result of the experiment and not the cause of the changes observed.

After the discovery and characterization of the phages and after introducing the dogma that the nucleic acid was the genome of all cells and viruses, the consensus was born, according to which such viruses must exist in humans and animals as well. In 1992, the dogma stating that the nucleic acid is the genotype of all cells was retracted in the scientific community. The ‘viral dogma’ of pathogenic viruses, however, is still being promoted today to the harm of billions of people. – for what?

The Bottom Line Concerning Phantom Viruses and the Polio and Measles Virus

[An Electron micrograph of the so-called Polio virus that has never been demonstrated scientifically to cause the symptoms of paralysis.  Illustration has been colorized for effect]

My bottom line still holds the truth that the terrain or internal environment is everything and the germ or so-called virus is NOTHING! The germ or so-called virus can only be a symptom of cellular breakdown due to an imbalance of the delicate alkaline pH balance of the body fluids and NOT the cause of that breakdown. That is why years ago I offered any scientist in the World a finders fee of 5 million US dollars if they could prove the existence of the HIV virus using Koch’s postulates. It has now been over 20 years and I am still waiting even though currently I no longer have the funds to pay the prize due to political assassination! It is unfortunate that a former 5 million US dollar prize offered 20 years ago was not enough money to change the current medical viral dogma that is currently paying out trillions of dollars to guess who?[281]

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Click here to read more: http://medcraveonline.com/IJVV/IJVV-02-00032.php

To order your copy of Second Thoughts About Viruses, Vaccines and the HIV/AIDS Hypothesis go to: https://www.amazon.com/…/ref=dbs_a_def_rwt_hsch_vapi_taft_p…

Second Thoughts About Cover copy

Lecture in Dubai – The 2nd Annual Conference on Bacterial, Viral and Infectious Diseases

http://www.drrobertyoung.com/events.html

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Join Robert O Young PhD and Galina Migalko MD in Dubai on June 18th and 19th, 2019 for the Annual Conference on Bacterial, Viral and Infectious Diseases. They will be Key Note Speakers and doing a workshop on the New Biology.

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For more information and to register go to: https://bacterialdiseases.infectiousconferences.com/organiz…

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The following is the abstract for Dr. Young’s lecture:

The Dismantling of the Viral Theory

Robert O Young CPT, MSc, DSc, PhD, Naturopathic Practitioner

Abstract

There is now over 100 years of documented history and research on the Polio virus and whether or not its treatment by inoculation has been successful in eradicating Polio. I am suggesting in this article and in my lecture that there are significant findings based on historical and past and current research, including my own that the viral theory of Polio and possibly other modern-day diseases, such as Post-Polio Syndrome, Polio Vaccine-Induced Paralysis, Legionnaires, CNS disease, Cancer, HIV/AIDS and now Zika may be caused by acidic chemical poisoning from DDT (dichloro-diphenyl-trichloroethane) and other related DDT pesticides, acidic vaccinations, and other factors including lifestyle and dietary factors rather than from a lone infectious virus. I will present ten historical graphs outlining the history of Polio, the production of DDT, BHC, Lead, Arsenic, Polio vaccinations and the author’s theory that chemical poisoning, vaccination, and lifestyle and dietary choices are a more likely causes for the symptoms of Polio, neurological diseases, Cancer, HIV/AIDS and now Zika.

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[2] Handbook of Pesticide Toxicology, edited by Wayland J. Hayes, Jr. and Edward R. Laws, Academic Press Inc., Harcourt Brace Jovanovich, Publishers, San Diego, 1991, p769

[3] Toxicological Profile: for DDT, DDE, and DDE. Agency for Toxic Substances and Disease Registry, September 2002.

[4] U. Beck, E. Löser “Chlorinated Benzenes and other Nucleus-Chlorinated Aromatic Hydrocarbons” Ullmann’s Encyclopedia of Industrial Chemistry, 2012, Wiley-VCH, Weinheim.

[5] Chlorobenzene”. Immediately Dangerous to Life and Health. National Institute for Occupational Safety and Health (NIOSH)

[6] U.S. Vital Statistics, U.S. Government Printing Office, Washington, D.C.

[7] Historical Statistics of the U.S., The U.S. Government Printing Office, Washington, D.C.

[8] Van Nostrand’s Encyclopedia of Science and Engineering (1995), vol. 5, p1725. The phrase “Pesticides As A Panacea: 1942-1962” is a subtitle found in Encyclopedia Britannica, Macropaedia (1986).

[9] Thomas, Robert E. (1955), Salt & Water, Power & People: A Short History of Hooker Electrochemical Co. Niagara Falls, NY: Hooker Chemical Co.

[10] Booth, Gerald (2000), “Ullmann’s Encyclopedia of Industrial Chemistry – Nitro Compounds, Aromatic”. doi:10.1002/14356007.a17_411. ISBN 3527306730

[11] Weber, Manfred; Weber, Markus; Kleine-Boymann, Michael (2004). “Ullmann’s Encyclopedia of Industrial Chemistry – Phenol”. doi:10.1002/14356007.a19_299.pub2. ISBN 3527306730.

[12] Haller, H. L., Bartlett, P. D., Drake, N. L., and others: The Chemical Composition of Technical DDT, American Chemical Society, Journal, volume 67, pages 1591- 1602, 1945.

[13] Jo-Yu Chin, Christopher Godwin, Chunrong Jia, Thomas Robins, Toby Lewis, Edith Parker, Paul Max, and Stuart Batterman, “Concentrations and Risks of p-Dichlorobenzene in Indoor and Outdoor Air,” Indoor Air, 2013 Feb; 23(1): 40–49, Published online 2012 Jul 18. doi: 10.1111/j.1600-0668.2012.00796.x.

[14] Duesberg, PH, “Inventing the AIDS Virus,” Regnery, (1996). ISBN 0-89526-399-8. [15] Icon Group International (Author), Chlorobenzene: Webster’s Timeline History, 1851 – 2007 May 17, 2010

[16] Ibid [17] Ibid

[18] Risse, GB (1988). Fee E, Fox DM, eds. Epidemics and History: Ecological Perspectives. in AIDS: The Burden of History. University of California Press, Berkeley. ISBN 0-520-06396-1.

[19] A Disease of Cleanliness: Polio in New York City, 1900-1990, in David Rosner, ed., Hives of Sickness: Public Health and Epidemics in New York City Rutgers University Press, 1995, pp. 115-130.

[20] McDonough, F., The Origins of the First and Second World Wars (Cambridge Perspectives in History), Cambridge University Press, August 28, 1997.

[21] Goel, A, Aggarwal, P, “Pesticide Poisoning,” Natl Med J India. 2007 Jul-Aug; 20(4):182-91.

[22] Ibid.

[23] Biskind, MS (1953) “Public Health Aspects of the New Insecticides,” American Journal of Digestive Diseases 20: 331-341.

[24] TIME Magazine, U.S. Edition, March 14, 1994 Vol. 143 No. 11. [25] Baily, J. W.: J. Am. Vet. M. A. 113: 251, Sept. 1948.

[26] Biden-Steele, K. and Stuckey, R. E.: “Poisoning by DDT Emulsion: Report of a Fatal Case”, Lancet, 2: 235-236, Aug. 17, 1946.

[27] Biskind, M. S.: “DDT Poisoning and X Disease in Cattle”, J. Am. Vet. M. A. 114: 20, Jan. 1949.

[28] Biskind, M. S.: “DDT Poisoning a Serious Public Health Hazard”, Am. J. Dig. Dis. 16: 73, Feb. 1949.

[29] Biskind, M. S.: “DDT Poisoning and the Elusive ‘Virus X’: A New Cause for Gastro- Enteritis”, Am. J. Dig. Dis. 16: 79, March 1949.

[30] Boyd, C. L.: “A Report on “XX Disease in Texas”, J. Am. Vet. M. A. 113: 463, Nov. 1948.

[31] Cameron, C. R., and Burgess, F.: “The Toxicity of DDT”, Brit. M. J. 1: 865-871, June 23, 1945.

[32] Carte; R. H., Hubanks, P. E., et al: “Effect of Cooking on the DDT Content of Beef”, Science, 107: 347, April 2, 1948.

[33] Case, R. A. M.: Toxic Effects of DDT in Man”, Brit. M. J., 2: 842-845, Dec. 15, 1945.

[34] Council on Pharmacy and Chemistry, A. M. A.: “Health Hazards of Pesticides”, J. A. M. A. 137: 1603, Aug. 28, 1948.

[35] Crescitelli, F., and Gillman, A.: “Electrical Manifestations of Cerebellum and Cerebral Cortex Following DDT Administration to Cats and Monkeys”, Am. J. Physiol., 147: 127- 137, Sept. 1946.

[36] Deederer, C.: “DDT Toxicity”, M.Rec. 161: 216-220, April 1948

[37] Domenici, T. J.: “Hepatitis without Jaundice and without Hepatomegaly”, N. Eng. J. Med. 240: 88, Jan. 20, 1949

[38] Dunn, J. E., Dunn, J. C., and Smith, R. S.: “Skin Sensitising Properties of DDT for 31

Guinea Pig”, Pub. Health Rep. 61: 1614-1620, 1949.

[39] Editorial: Pesticides: “Chemical Contaminants of Foods”, J.A.M.A. 137: 1604, Aug. 28, 1948.

[40] Fitzhugh, O. G., and Nelson, A. A.: “The Chronic Oral Toxicity of DDT”, J. Pharm.acol. and Exper. Therap. 89: 18-30, Jan. 1947.

[41] Gamier, G.: “Treatment of Scabies with DDT”, .Presse Med. 56: 458, June 23, 1948. [42] Garett, ii. M., “Toxicity of DDT for Man”, Alabama St. M. A. J., 17: 74, Aug. 1947.

[43] Globus, J. H.: “DDT Poisoning; Histopathologic Observations on the Central Nervous System in So-Treated Monkeys, Dogs, Cats and Rats”, J. Neuropath. 7: 418-431, Oct. 1948.

[44] Haymaker, W., Ginzler, A. M., and Ferguson, J. L.: “Toxic Effects of Prolonged Ingestion of DDT on Dogs, with Special Reference to Lesions in Brain”, Am. J. M. Sc. 212: 423, Oct. 1946.

[45] Hill, K. R., and Daniiani, C. R.: “Death Following Exposure to DDT, Report of a Case”, New Eng. J. Med., 235: 897-899, Dec. 19, 1946.

[46] Hill, K. 3. and Robinson, G.: “A Fatal Case of DDT Poisoning in a Child, with an Account of Two Accidental Deaths in Dogs”. Brit. M. J. 2: 845-847, Dee. 15, 1945.

[47] Ingle, L.: “Toxicity of Chlordane to White Rats”, J. Econ. Entomol. 40: 264-268, 1947.

[48] Jandorf, B. J;. Sanett, H. P., and Bodansky, Oscar: “Effect of Oral Administration of DDT on Metabolism of Glucose and Pyruvie Acid in Rat Tissues”, J. Pharmaeol. and Exper. Therap. 88: 333-337, Dec. 1946.

[49] Jenkins, D. W.: “A Review of the Insecticide Hexachloro-cyclohexane (‘666’)”, Office of Technical Services, U. S. Dept of Commerce, Washington, D • C., No. PB 4034, Med. Div. Rept. No. 56, Sept. 26, 1945.

[50] Kempe, H. E.: “Progress Report on Benzene Hexachloride for the Destruction of Sheep Scab Mites”, Vet. Med., Feb. 1948, pp. 76-79.

[51] Kirk, H.: Vet. Red. 58: 43, 1946.

[52] Kirk, H.: “DDT in Canine Practice”, Vet. Med. Feb. 1947, PP. 76-78.

[53] Lawhon, G. J., Jr.: “X Disease in South Carolina”, N. Am. Vet. 29: 643, Oct. 1948.

[54] Leider, M.: “Allergenic Eczematous Contact-Type Dermatitis Caused by DDT”, J. Invest. Dermatol. 8: 125-126., March 1947.

[55] Lillie, R. D., Smith, M. I., and Stohlman, E. F.: Pathologic Action of DDT and Certain of its Analogs and Derivatives”, Arch. Path. 43: 127-142, Feb. 1947.

[56] Mackerras, I. M., and West, R. F. K.: “DDT Poisoning in Man”, M. J. Australia, 1: 400-401, March 23, 1946.

[57] Mobbs, J. F.:” Toxicity of Hexaehloroeyclohexane in Scabies, J.A.M.A. 138: 1253, Dec. 25, 1948. Personal Communication.

[58] Morrill, C. C.: “Hyperkeratosi.s or X Disease”, N. Am. Vet. 29: 642, Oct. 1948.

[59] Neal, P. A., Sweeney, T. B., Spicer, S. S., and von Oettingen, W. F.: “The Excretion of DDT in Man, Together with Clinical Observations”, Pub. Health Rep., 61: 403, March 22, 1946.

[60] Neal, P. A., von Oettingen, W. F., Smith, W. W., et al: Toxicology and Potential Dangers of Aerosols, Mists and Dusting Powders Containing DDT”, Pub. Health Rep. Suppl. 177, 1944.

[61] Neal, P. A., von Oettingeu, W. F., Dunn, R. C., and Sharpless, N. E.: “Toxicology and Potential Dangers of Aerosols and Residues from Aerosols Containing 3 Percent of DDT. Second Report, ibid., Suppl. 183, 1945.

[62] Nelson, A. A., Draize, 3. H., Woodard, G., et al: “Histopathological Changes Following Administration of DDT to Several Species of Animals”, U. S. Pub. Health Rep. 59: 1009, Aug. 4, 1944.

[63] Neve, Helen: “Toxic Effects of DDT on a Cat”, Vet. Rec. 58: 43, 1946. Vet. Med., Feb. 1947, p. 78.

[64] Niedelman, M. L.: “Contact Dermatitis Due to DDT”, Occup. Med. 1: 391-395, April 1946.

[65] Radeleff, R. D.: “DDT Spray Outmodes Dipping Vat”, Vet. Med. Oct. 1947, pp. 372- 373.

[66] Radeleff, R. D.: “Chlordane Poisoning: Symptomatology and Pathology, Vet. Med. Aug. 1948, pp. 342-347.

[67] Robinson, J. H.: “Harvest Analysis of DDT Residues”, Food Packer, 29: 50-53, 1948.

[68] Riker, W. F., Jr., Huebner, Virginia, R., Raska, S. B., and Cattell, McKeen: “Studies on DDT, Effects on Oxidative Metabolism”, J. Pharmacol. and, Exper. Therap., 88: 327- 332, Dec. 1946.

[69] Sarrett, H. P., and Jandorf, B. J.: “Effects of Chronic DDT Intoxication in Rats on Lipids and Other Constituents of Liver”, ibid., 91: 340-344, Dec. 1947.

[70] Smith, M. I.: “Accidental Ingestion of DDT, with a Note on its Metabolism in Man”, J.A.M.A., 131: 519-520, Juno 8, 1946.

[71] Smith, M. I., and Stohlnian, E. F.: “Pharmacologic Action of 2, 2 his (p-Chlorophenyl) 1,1,1-Trichloroethane and its Estimation in the Tissues and Body Fluid”, Pub. Health Rep., 59: 984, July 28, 1944.

[72] SmIth, M. I., and Stohlman, E. F.: “Further Studies on the Pharmacologic Action of DDT”, ibid., 60: 289, March 16, 1945.

[73] Smith, N. 3.: “Death Following Accidental Ingestion of DDT”, J.A.M.A., 136: 469- 471, Feb. 14, 1948.

[74] Smith, R. F., Fullmes, O. H., and Messenger, P. S.: “DDT Residues on Alfalfa Hay and Seed Chaff”, J. Econ. Entomol. 41: 755-8, 1948.

[75] Strycker, G. V., and Godfroy, B.: “Dermatitis Resulting from Exposure to DDT”, J. Missouri St. M. A., 43: 384-386, June 1948.

[76] Taylor, E. L.: “Danger of Ununction with DDT”, Lancet, 2: 320, Sept. 8, 1945.

[77] Telford, H. S., and Guthrie, J. E.: “Transmission of the Toxicity of DDT Through the Milk of White Rats and Goats”, Science, 102: 647, Dec. 21, 1945.

[78] Thoungh, TI. C.: “Poisonous Effects of DDT on Humans”, Indian M. Ga:. 81: 432, Oct. 1946.

[79] U. S. Dept. Agriculture, “Bureau of Entomology and Plant Quarantine: Now Insecticides in Grasshopper Control”, Bull. E-722, May 1947. Bull. EC.1, March 1948.

[80] U. S. Dept. Agriculture, Bureau of Entomology and Plant Quarantine: “New Insecticides for Controlling External Parasites of Livestock”, Bull. E. 762, Dec. 1948.

[81] Westerfteld, C.: “The Use of DDT in Medicine-A Review”, Vet. Med., Oct. 1946, pp. 355-360.

[82] Wigglesworth, V. D.: “A Case of DDT Poisoning in Man”, Brit M. J. 1: 517, April 14, 1945.

[83] Wilson, J. B.: Are Pesticides Making Your Food Unsafer? Hygiea, Jan. 1949. p. 44.

[84] Woodard, G., Ofner, Ruth B., and Montgomery, C. M.: “Accumulation of DDT in the Body Fat and its Appearance in the Milk of Dogs”, Science, 102: 177-178, Aug. 17, 1945.

[85] Wright, C. S., Doan, C. A., and Haynie, H. C.: “Agranulocytosis Occurring after Exposure to DDT Pyrethrum Aerosol Bomb”, Am. J. Med., 1: 562-567, Nov. 1946.

[86] The Pesticide Residues Amendment of 1954, Pub. L. No. 83-518, ch. 559, 68 Stat. 511 [codified at 21 USC § 346a (1981)]; and the Food Additives Amendments of 1958, Pub. L. No. 85-529, Ch. 4.72 Stat. 1785 [codified at 21 USC § 348 (1981)], respectively.

[87] 20 Fed. Reg. 750 (1955) [codified until repealed at 21 CFR § 120. 1(f) (1956). [88] DDT Regulatory History: A Brief Survey (to 1975). United States Environmental

Protection Agency (EPA).

[89] Ibid.

[90] TIME Magazine, U.S. Edition, March 14, 1994 Vol. 143 No. 11.

(91] Handbook of Pesticide Toxicology, edited by Wayland J. Hayes, Jr. and Edward R. Laws, Academic Press Inc., Harcourt Brace Jovanovich, Publishers, San Diego, 1991.

[92] Peter Duesberg and Brian J. Ellison, Inventing the AIDS Virus, Regnery Pub.,1996. [93] Ibid.

[94] Biskind, MS (1953) “Public Health Aspects of the New Insecticides,” American Journal of Digestive Diseases 20: 331-341.

[95] Peter Duesberg and Brian J. Ellison, Inventing the AIDS Virus, Regnery Pub.,1996. [96] DDT Regulatory History: A Brief Survey (to 1975). United States Environmental

Protection Agency (EPA).

[97] Poliomyelitis: Fact sheet N°114″. World Health Organization. Sep 2016. Retrieved 14 Sep 2016.

[98] Ibid.

[99] DDT Regulatory History: A Brief Survey (to 1975). United States Environmental

Protection Agency (EPA).

[100] Ibid.

[101] Handbook of Pesticide Toxicology, edited by Wayland J. Hayes, Jr. and Edward R.

Laws, Academic Press Inc., Harcourt Brace Jovanovich, Publishers, San Diego, 1991.

[102] Rea WJ, Johnson AR, Fenyves E, Butler J. Related Articles: The environmental aspects of the post-polio syndrome. Birth Defects Orig Artic Ser. 1987;23(4):173-81. No abstract available. Pub Med ID: 3620615; UI: 87299998.

[103] Ibid.

[104] Casarett and Doull’s Toxicology (1996).

[105) Rea WJ, Johnson AR, Fenyves E, Butler J. Related Articles: The environmental aspects of the post-polio syndrome. Birth Defects Orig Artic Ser. 1987;23(4):173-81. No abstract available. Pub Med ID: 3620615; UI: 87299998.

[106] PubMed ID: 7611631, UI: 95336052 (London, May, 1995)

[107] Pub Med ID: 7611630, UI: 95336051 (Bethesda, MA, May, 1995)

[108] Pub Med ID: 8818905, UI: 96415998 (Lyon, France, Aug., 1996)

[109] Alfredo Morabia (1 January 2004). A History of Epidemiologic Methods and Concepts. Springer. pp. 133–4. ISBN 978-3-7643-6818-0. Retrieved 22 June 2013.

[110] Ibid.

[111] Morton S. Biskind, MD. “Public Health Aspects of the New Insecticides”. American

Journal of Digestive Diseases, New York, 1953, v 20, p331. [112] Ibid.

[113] Young RO (2016) Second Thoughts Concerning Viruses, Vaccines and the HIV/AIDS Hypothesis – Part 2. Int J Vaccines Vaccin 2(3): 00034. DOI: 10.15406/ijvv.2016.02.00034

[114] Dirt and Disease: Polio before FDR Rutgers University Press, 1992. [115] Ibid.

[116] Menkes, John H., Child Neurology, pg. 420, (1995).

[117] A Paralyzing Fear: The Story of Polio in America. Produced by Paul Wagner, Nina Gilden Seavey. Directed, written by Nina Gilden Seavey. Narration written by Stephen Chodorov. With: Narrator: Olympia Dukakis. Camera (Colorlab color), Allen Moore, Reuben Aaronson; editor, Catherine Shields; music, Paul Christianson; associate producers, Tom Wentworth, Malvina Anderson Martin. Reviewed on videocassette, N.Y., March 3, 1998. Running time: 90 min.

[118] FILM REVIEW; Once a Fear Beyond Fear Itself, by STEPHEN HOLDEN, Published: March 4, 1998, New York Times.

[119] Ibid.

[120] Duesberg, Peter and Ellison, Brian J., Inventing the AIDS Virus, Regnery Pub.,1996.

[121] Ibid.

[122] Ibid.

[123] Ibid.

[124] Ibid.

[125] Rose DR (2004). “Fact Sheet—Polio Vaccine Field Trial of 1954.” March of Dimes Archives. (2004).

[126] Ibid.

[127] American Journal of Digestive Diseases, 1953 20:330 [128] Ibid.

[129] Ibid.

[130] Jenkins, D. W.: “A Review of the Insecticide Hexachloro-cyclohexane (‘666’)”, Office of Technical Services, U. S. Department of Commerce, Washington, D.C., No. PB 4034, Med. Div. Rept. No. 56, Sept. 26, 1945.

[131] Biskind, M., “DDT Poisoning and the Elusive ‘Virus X’.” A New Cause for Gastroenteritis.” Am. J. Dig., Vol. 16, Num 3, pg. 79-84, (1949).

[132] Biskind, MS, Bieber, I, “DDT Poisoning A New Syndrome With Neuropsychiatric Manifestations,” American Journal of Psychotherapy, p261, (1949).

[133] Presented before the Select Committee to Investigate the Use of Chemicals in Food Products, United States House of Representatives, U.S. December 12, 1950 Westport, Conn.

[134] “Salk and Sabin: poliomyelitis immunisation”. J Neurol Neurosurg Psychiatry. 75 (11): 1552. doi:10.1136/jnnp.2003.028530. PMC 1738787. PMID 15489385.

[135] H. Rept. No. 2356, 82d Cong., 2d sess. 1 (1952), reprinted in A Legislative History of the Federal Food, Drug and Cosmetic Act and Its Amendments 499 (hereinafter Legislative History)

[136] Scobey, RR, “Is The Public Health Law Responsible For The Poliomyelitis Mystery?” Syracuse, N.Y., Archive of Pediatrics (May, 1951).

[137] White, Mark; Sharon M. McDonnell; Denise H.Werker; Victor M. Cardenas; Stephen B. Thacker (2001). “Partnerships in International Applied Epidemiology Training and Service,”. American Journal of Epidemiology 154 (11): 993–999. doi:10.1093/aje/154.11.993.

[138] Van Nostrand’s Encyclopedia of Science and Engineering, Van Nostrand Reinhold 1995, v 5, p1775

[139] “Salk and Sabin: poliomyelitis immunisation”. J Neurol Neurosurg Psychiatry. 75 (11): 1552. doi:10.1136/jnnp.2003.028530. PMC 1738787. PMID 15489385.

[140] Ralph R. Scobey, MD. “The Poison Cause of Poliomyelitis and Obstructions to Its Investigation.” Archive of Pediatrics, April 1952.

[141] The National Adipose Tissue Survey, reported in Handbook of Pesticide Toxicology, edited by Wayland J. Hayes, Jr. and Edward R. Laws, Academic Press Inc., Harcourt Brace Jovanovich, Publishers, San Diego, 1991, pg. 303.

[142] The National Adipose Tissue Survey, reported in Handbook of Pesticide Toxicology, edited by Wayland J. Hayes, Jr. and Edward R. Laws, Academic Press Inc., Harcourt Brace Jovanovich, Publishers, San Diego, 1991, pg. 303.

[143] Van Nostrand’s Encyclopedia of Science and Engineering (1995), vol. 5, pg.1725. [144] Offit, Paul A. (2007). The Cutter Incident: How America’s First Polio Vaccine Led to

the Growing Vaccine Crisis. Yale University Press. p. 38. ISBN 0-300-12605-0. [145] Albert Sabin to Henry Kumm, Sabin Papers, UC, Pittsburgh Press, 1954. [146] American Journal of Digestive Diseases, 1953 20:330.

[147] Trevelyan, B., Smallman-Raynor, M. and Cliff, A.D., The Spatial Dynamics of Poliomyelitis in the United States: From Epidemic Emergence to Vaccine-Induced Retreat, 1910–1971, Ann Assoc Am Geogr. 2005 Jun; 95(2): 269–293.

[148] Baicus, A., History of Polio Vaccination, World J Virol. 2012 Aug 12; 1(4): 108–114. Published online 2012 Aug 12. doi: 10.5501/wjv.v1.i4.108.

[149] Ibid.

[150] Women’s History Month: “Oveta Culp Hobby” by Senator Kay Bailey Hutchison

Humanities Texas, March 2012.

[151] Harry M. Marks, “The 1954 Salk Poliomyelitis Vaccine Field Trial,” Institute of the History of Medicine, Johns Hopkins University, Baltimore, MD: 2008.

152[ National Museum of American History, “Whatever Happened to Polio?” Time line, http://americanhistory.si.edu/polio/timeline/index.htm (accessed March 28,, 2012).

[153] Abid.

[154] Norrby E., Prusiner S.B., Polio and Nobel Prizes: looking vack 50 years. Ann Neurol.

2007 May;61(5):385-95.

[155] Eloise Batic, You Are There 1955: Ending Polio exhibit text (2012).

[156] Boston Herald newspaper, April 18, 1955, “Drug Companies Expecting Big Profit on

Salk Vaccine”,

[157] Washington Bureau of the Detroit Free Press reports, June 3, 1955.

[158] Michigan University. Poliomyelitis Evaluation Center (1955), An evaluation mof the 1954 poliomyelitis vaccine trials; summary report. Ann Arbor: n.p. , pp. 17-18 as quoted in Marks, Harry M. “The 1954 Salk Poliomyelitis Vaccine Field Trial.” Institute of the History of Medicine, Johns Hopkins University. Baltimore: 2008, p. 20.

[160] McBean E. The Poisoned Needle. Mokelumne Hill, California: Health Research,1957:1

[161] McBean E. The Poisoned Needle. Mokelumne Hill, California: Health Research, 1957:119.

[162] McBean E. The Poisoned Needle. Mokelumne Hill, California: Health Research,1957:1

[163] Offit, Paul A. The Cutter Incident: How America’s First Polio Vaccine Led to the Growing Vaccine Crisis, Yale University Press, 2005, pp. 100, 116–19, 133. ISBN 0-300- 10864-8

[164] Ibid.

[165] Smith, JS, “Patenting the Sun: Polio and the Salk Vaccine,” 1st Edition, William

Morrow & Co; 1st edition (April 1990).

[166] Offit PA (2005), “The Cutter incident, 50 years later” (PDF). N. Engl. J. Med. 352 (14): 1411–1412. doi:10.1056/NEJMp048180. PMID 15814877

[167] McBean E., The Poisoned Needle. Mokelumne Hill, California: Health Research,1957:1.

[168] Harris RJ et al Contaminant viruses in two live vaccines produced in chick cells. J Hyg (London) 1966 Mar:64(1) : 1-7

[169] McBean E. The Poisoned Needle. Mokelumne Hill, California: Health Research,1957:1

[170] Ibid.

[171] Ibid.

[172] Ibid.

[173] Ii. Results. American journal of public health and the nation’s health. 1955;45:15–48. [PMC free article] [PubMed]

[174] Harper’s Magazine. “’Who is responsible, and why, for the chaotic confusion over the polio inoculations?’ A noted medical journalist disentangles the essential facts.” August, 1955.

[175] Ibid.

[176] Ibid.

[177] American Cancer Society, Volume 8, Issue 1, Pages 1–218, (1955).

[178] Paul JR. A history of poliomyelitis. New Haven, CT: Yale University Press; 1971.

[179] Ibid.

[180] Ibid.

[181] Ibid.

[182] Rogers N. Dirt and disease: Polio before fdr. New Brunswick, NJ: Rutgers University Press; 1992.

[183] Ibid.

[184] Smith, Derek R; Leggat Peter A (2005). “Pioneering figures in medicine: Albert Bruce Sabin–inventor of the oral polio vaccine”. The Kurume medical journal. 52 (3): 111–6. doi:10.2739/kurumemedj.52.111. PMID 16422178

[185] Rose, David, March of Dimes Archives, August 26, 2010. http://www.marchofdimes.org/mission/a-history-of-the-march-of-dimes.aspx

[186] American Journal of Public Health and the Nations Health: May 1956, Vol. 46, No. 5: 547–562. Citation | PDF (2177 KB) | PDF Plus (744 KB)

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[190] Curtis T, Manson P. Scientist’s Polio Fear Unheeded: How U.S. Researcher’s Warning Was Silenced. The Houston Post 1992:A1 and A12.

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[195] Bookchin D, Schumaker J. Tainted Polio Vaccine Still Carries Its Threat 40 Years Later. The Boston Globe, January 26, 1997.

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[272] Siehe Ausführungen zu Virchows Leben und Wirkung in WissenschafftPlus Nr. 5/2015 und Nr. 6/2015. 2 Anticontagionism between 1821 and 1867.

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[279] Siehe WissenschafftPlus Nr. 1/2014.

[280] Zur Geschichte der frühen Virusforschung. Übersichtsarbeit von Prof. Karlheinz Lüdtke. Reprint 125 des MAX-PLANCK-INSTITUT FÜR WISSENSCHAFTSGESCHICHTE, 89 Seiten, 1999.

[281) The government of the United States of America holds patents on the following viruses: Ebola, Patent number #CA2741523A1, Swine Flu, Patent number 8124101, HIV, Patent number #5676977, the cure for cancer, Patent number #6630507.