Sep 13, 2019

Cannabis for fibromyalgia & nerve pain






Cannabis has been used as an all-purpose homeopathic remedy for centuries. Over time, evidence suggests that the plant was an herbal remedy for psycho-neurological disordersbreast cancerrheumatism sexual disorders, and painful complications related to childbirth. Now, this ancient tool has a new, modern application. A cannabis patch is now available for patients with fibromyalgia and diabetic nerve pain.

Cannabis for fibromyalgia & nerve pain



Fibromyalgia and diabetic neuropathy have a couple of things in common. Both conditions involve seemingly unexplainable pain, tingling, and can drastically reduce your quality of life.
Early research suggests that cannabis may have powerful therapeutic effects for both conditions, and this new pain patch offers a novel new approach for conditions that are incredibly difficult to treat.
2014 survey from the National Pain Foundations found that cannabis was considered the most effective pain medication by fibromyalgia patients who were willing to experiment with the herb.
Not all survey respondents had consumed cannabis. However, those that had suggested that the herb worked better at managing pain than the leading prescriptions for fibromyalgia, including Savella, Cymbalta, and Lyrica.
Small human trials of cannabis for diabetic neuropathy have also been successful. A study of 16 patients with diabetic neuropathy of the feet found the herb successfully reduced pain symptoms in a dose-dependant manner. The cannabis plant has successfully reduced nerve pain associated with conditions like multiple sclerosis as well.
While expensive cannabis-based pharmaceuticals are already available in some countries for the treatment of nervous disorders, most canna-curious patients are stuck with topical creams and oral cannabis options, which can be a little strong for the daytime.
Now, one innovative company, Cannabis Science, has released a revolutionary new topical application of cannabis medicines.

Cannabis Science designs an infused pain patch



Cannabis Science, Inc. is a pharmaceutical research company that works to develop innovative new cannabis medicines. In November of 2016, they announced their most recent project, a transdermal patch that delivers powerful pain-fighting medicine through the skin and into the bloodstream.
The company has two new patches in mind, one for fibromyalgia and one for diabetic neuropathy. While both of these patches will contain cannabinoids, each formulation and delivery method will be designed to most effectively manage symptoms of the respective illness.
In a press release announcing the new pain patch, Cannabis Science CEO Raymond Dabney explains,
The development of these two new pharmaceutical medicinal applications are just the tip of the iceberg for what we see as the future for Cannabis Science.
While we strive to increase our land capacity for growth and facilities to produce our own product to supply our scientists with proprietary materials to make these formulations, we are also busy researching more potential needs for Cannabis related medical applications and developing the methods for delivery of these medications.
Earlier in 2016, Cannabis Science began recruiting for a study on inhaled cannabis preparations for patients with asthma and lung diseases like COPD.
Cannabis Science is also not the first company to look into the transdermal applications of cannabis. Mary’s Medicinals got there first, offering cannabis-infused pain patches to medical cannabis patients in Colorado, Arizona, Nevada, Washington, Michigan, and Oregon. The company also hopes to offer their patches in California soon.
Post Polio Litaff, Association A.C _APPLAC Mexico

Sep 10, 2019

The Polio Paradox Richard Bruno H.D



Excerpts from The Polio Paradox, 2002, by Richard L. Bruno who estimated 1.63 million polio survivors in the US. [p6] “There were more polio survivors than those with Parkinson’s disease, multiple sclerosis and spinal cord injury combined”…”the cause and treatment of PPS involved both body and mind”, or Dr. Bruno’s specialty: physicopsychology, for which he holds a PhD.

[p12] “There are clear parallels dating from as far back as 1935 between polio and what in the 1980s came to be called Chronic Fatigue Syndrome”…”Twenty million more individuals with a variety of disabilities..are also experiencing fatigue, muscle weakness, and pain in mid-life, and seeing their abilities ebb away”

[p15] “In 1875 an unusual case was presented to the Society of Biology in Paris. A nineteen-year-old patient had had polio when he was six months old that paralyzed his left side…The young man had recovered partial use of his left arm and leg and became a tanner, which required him to use his arms to pull heavy, wet hides out of vats of acid. By the time he was seventeen, this French patient reported fatigue and a feeling of heaviness in his right arm, the arm that had apparently not been affected by the polio. His right arm and leg both became weaker and smaller”…

   On hearing this presentation, the renowned French neurologist Jean-Martin Charcot concluded that the young tanner’s new weakness was due to overusing his stronger right arm, damage done by the poliovirus somehow having ‘moved’ from the left side of his body to the right.

   That same year, three other French doctors described other polio survivors who had developed muscle weakness and atrophy, a shrinking of the muscles, fifteen to almost thirty years after they had polio. From 1875 to 1900, twenty-four articles appeared in European medical journals describing 30 additional polio survivors experiencing new weakness and sometimes atrophy..in limbs that obviously had been affected during the polio attack, but also in limbs that had..been unaffected. In 1899 British doctor William Hirsch reviewed all the cases reported during the nineteenth century. He concluded that there were three possible causes for late-onset weakness in polio survivors: 

(1) The poliovirus had damaged spinal cord motor neurons –the cells that make muscles contract– making them vulnerable to some other disease later in life; (2) Certain individuals were susceptible to developing motor neuron diseases..that allowed them to get polio as children and then develop another disease called ‘progressive muscular atrophy’ later in life; (3) Spinal cord motor neurons had been ‘scarred’ by the poliovirus, setting the stage for a ‘flare-up’ at a later date which caused new weakness.

[p16]  Hirsch was the first to suggest that the poliovirus could somehow damage neurons early in life, damage that..caused new muscle weakness many years later.

   In 1903 Charles Potts wrote the twentieth century’s first article on the late effects of polio –the first to appear in an American medical journal in which he too reviewed the nineteenth-century cases. Potts concluded that two of the polio survivors described had ALS –amyotrophic lateral sclerosis..(Lou Gehrig’s disease)– a fatal disease that causes progressive paralysis of muscles throughout the the body as a result of the death of the spinal cord motor neurons. However, Potts added that the overwhelming majority of the polio survivors described thus far..did not have ALS but instead had progressive muscular atrophy [as] Hirsch had mentioned, a disease of unknown origin…

In 1936, New York neurologists Salmon and Riley..supposed..the new and frightening notion that the poliovirus might lie dormant in the spinal cord and somehow cause muscle weakness decades later…

[p17] The dearth of articles between 1936 and 1960 about the late effects in polio survivors is undoubtedly due to polio’s incidence reaching epidemic proportions. All of medicine was focused on dealing with the acute problems being experienced by the hundreds of thousands of individuals infected with the poliovirus during those years, and on developing a polio vaccine. But articles about late-onset problems appeared again. A 1962 British paper by K.J. Zilkha was the first to follow the course of muscle weakness in polio survivors over many years…

In 1970, three British lung specialists reported…polio patients who were experiencing not only muscle weakness but also “excessive fatigue”, “breathlessness”, an inability to concentrate, drowsiness, and “severe attacks of sleepiness”. These patients also reported “abnormal sensitivity to cold, especially of the extremities”…

[p18] And in 1980 a group of Italian doctors…concluded that although only one hundred cases had been described in the preceeding 105 years, late-onset problems in polio survivors were “far from rare”. They agreed..that late-onset symptoms represented a “new process distinguishable from the old disease”.

Chapter Three “The Guided Missile”…
[p20].. quoting researcher David Bodian: “The average number of spinal cord motor neurons that are destroyed by the poliovirus is almost 50%. However, nonparalytic polio may be associated with severe neuron damage in the spinal cord. What is more, some with nonparalytic poliomyelitis do not have any damage in the spinal cord but have charateristic damage in the brain, which is more extensive than in some who did have paralysis. All available evidence shows conclusively that every case of polio exhibits damage in the brain. The poliovirus is capable of producing an encephalitis, with or without symptoms, in the absence of any damage to the spinal cord. As far as the pathologist is concerned all cases of polio are encephalitic”.
[p21] It’s amazing that something so small can do so much damage…But the poliovirus doesn’t attach to and damage just any cell. It is a ‘guided missile’ that does one thing: seek out, damage, and destroy the neurons that “activate” you –the ones that activate your brain and muscles. The poliovirus is the perfect human “Off switch”…

[p23]  The existence of dozens of poliovirus strains makes it clear that polioviruses mutate inside people and can change their virulence. In fact, experiments in animals show that the passage of poliovirus –infecting one animal with a poliovirus, having that animal infect another, and so on– can increase virulence. As polioviruses passed from person to person during the middle of the twentieth century, they apparently became more virulent, causing more paralysis and killing more people in 1950 than they did in 1920…

[p24]…Poliovirus released from both your tonsils and intestines also traveled to the large lymph nodes under your arms…finally, about ten days after you were infected..huge amounts of virus spilled into your bloodstream..[carrying] its deadly cargo toward its intended destination : the neurons in your brain and spinal cord.

[p25]  Virus-laden blood flowed up into your head and found “leaky” places in the brain’s blood vessels, where poliovirus flowed into the brain. At the same time, infected monocytes passed throught the walls of brain blood vessels acting like ‘poliovirus taxis’ that also allowed virus to enter the brain…

[p26] Once inside those neurons..[they] travelled inside neurons to penetrate more deeply…Then the poliovirus could head south, descending inside spinal cord neurons and ending up in the motor neurons…

   There’s yet a third way poliovirus could reach brain and spinal cord motor neurons…such as [flowing] out of the Peyer’s patches and enter the vagus nerve –the nerve that makes the intestines contract– inside which they can travel all the way up to the brain…What’s more, motor neurons are covered with poliovirus receptors where they make contact with your muscles. When your blood was full of virus, damaging a muscle and puncturing a blood vessel could bathe neurons with virus…children whose muscles had been slightly daamaged by an injection were up to ten times more likely to get paralytic polio –and were most often paralyzed in the limb where they received the injection.
   After a poliovirus latches on..to the surface of a neuron [it] causes it to ‘unzip’, releasing its contents inside the neuron. [These are] about a dozen individual proteins..that shut down and then literally break apart the ‘factories’ that manufacture [what] a neuron needs…

[p27]..the neuron can no longer make neurochemicals –the proteins that allow one neuron to talk to another and that allow motor neurons to make muscles contract. When neurochemicals stop being made, the neuron’s ‘OFF’ switch id thrown.

[p29] The poliovirus is remarkable in its ability to invade neurons. In the 1940s..Bodian found that 96% of motor neurons were infected by the poliovirus if you had any paralysis at all!

   But..on average, 50% of all motor neurons are destroyed…Bodian discovered that at least 60%..must be killed before [a] muscle shows any weakness at all.

[p30] Unfortunately, there’s even more to the aftermath of polio than losing about half of your motor neurons…those recovered neurons were never the same as they were before the poliovirus invaded. Damaged and rebuilt neurons are smaller and also have shrunken axons –the cable-like extensions that travel out..to connect with muscles.

[p31] What’s more, the microscopic tubules within the neurons were ‘plugged’ with debris that was probably created when the poliovirus broke apart the neuron…like clogged pipes, plugged tubules can’t carry all the proteins, nutrients, and neurochemicals where they need to go…

[p33] In Latin,[Greek actuallypolio means ‘gray’…gray neurons are those not covered in myelin, the white fatty insulation that separates one neuron from another….

[p34]..In fact, the main event of the poliovirus attack was not in the spinal cord at all. [more excerpts on The Polio Paradox page]

Sep 9, 2019

Pakistan’s First WhatsApp Polio Helpline-




 Our government has become digitised; it is evident from the no of reforms we have seen form last some years. We have come across plenty of apps that are launched specially for the citizens of Pakistan in order to make their lives easier. Be it app to fight harassment or app for moon sighting and this Pakistan’s First WhatsApp Polio Helpline; these are the best reforms any country can enjoy.

Government Launches Pakistan’s First WhatsApp Polio Helpline

Yesterday, PM’s focal person on Polio Babar Bin Atta announced the launch of first-ever WhatsApp helpline in Pakistan would help people with polio related queries. Through this app, people will be able to ask multiple questions regarding the polio programme and will also be able to lodge complaints. This app also facilitates people to report if their child has missed out an anti-polio campaign in any part of Pakistan. It is the best thing a mother can do while sitting in their comfort zone.
While telling about the newly launched feature, Mr Babar tweeted that:
“Another First Ever by Pakistan Polio Programme. 24/7 WhatsApp Polio Helpline. Any question? Missed children? Misconceptions? Complaints? We are at your service with just a simple WhatsApp message. 0346 – 7776546,”


After this tweet, he also requested people to send queries related to polio or this app on the WhatsApp helpline.
“Dear brothers & sisters this is a WhatsApp text helpline, since my tweet, there is a flurry of calls on the number. Please don’t call, just send your query via WhatsApp Text,”
Well-done! An outstanding initiative, soon we will be living in a country which will be free of all such kinds of diseases.

Everything You Learned About the Cause of Polio is Wrong



Originally titled, "A Critique Of Scientific Literature: Pesticides and Polio," this article by Jim West was first published in The Townsend Letter for Doctors and Patients, June 2000, then republished as a 2nd edition in 2002 by The Weston A. Price Foundation, with additional material and the editorship of Sally Fallon. The article summarizes his book, "DDT/Polio", which he had attempted to publish in 1998. This is a 3rd edition, August 14, 2015.


Warning 
It has been alleged that DDT causes or contributes to a wide variety of diseases of humans and animals not previously recognized as associated with any chemical. Such diseases included... poliomyelitis, ...such irresponsible claims could produce great harm and, if taken seriously, even interfere with scientific search for true causes...[1] (Handbook of Pesticide Toxicology, edited by Wayland J. Hayes, Jr. and Edward R. Laws, 1991)
Hayes and Laws were informing their readers about the heretic, Dr. Morton S. Biskind.
In 1953, when Biskind's writings were published, the United States had just endured its greatest polio epidemic. The entire public was steeped in dramatic images -- a predatory poliovirus, nearly a million dead and paralyzed children, iron lungs, struggling doctors and dedicated nurses. The late president Franklin D. Roosevelt had been memorialized as a polio victim who was infected with the deadly poliovirus near the beautiful and remote island of Campobello. The media was saturated with positive images of scientific progress and the marvels of DDT to kill disease-carrying mosquitoes. Jonas Salk was in the wings, preparing to be moved center stage.
Through this intellectually paralyzing atmosphere, Dr. Biskind had the composure to argue what he thought was the most obvious explanation for the polio epidemic: Central nervous system diseases such as polio are actually the physiological and symptomatic manifestations of the ongoing government and industry sponsored inundation of the world's populace with central nervous system poisons.
Today, few remember this poignant writer who struggled with the issues of pesticides, issues that Rachel Carson would be allowed to politely bring to public awareness nine years later, as the lead story in The New Yorker magazine and then as a national best seller, by limiting her focus to the environment and wildlife. Biskind had the audacity to write about human damage.
I found "M.S. Biskind" in the endnotes to Hayes' and Laws' diatribe. What could possibly have motivated Hayes' and Laws' biased genuflection towards germ theory? Such offerings, commonly written into the final paragraphs of scientific articles, are usually done with an appearance of impartiality. With great anticipation, I went to a medical library and found Biskind's 10-page 1953 article in the American Journal of Digestive Diseases.[2] Presented below are excerpts regarding polio from his article.
In 1945, against the advice of investigators who had studied the pharmacology of the compound and found it dangerous for all forms of life, DDT (chlorophenoethane, dichlorodiphenyl-trichloroethane) was released in the United States and other countries for general use by the public as an insecticide. 
[...]
Since the last war there have been a number of curious changes in the incidence of certain ailments and the development of new syndromes never before observed. A most significant feature of this situation is that both man and all his domestic animals have simultaneously been affected.
In man, the incidence of poliomyelitis has risen sharply; 
[...]
It was even known by 1945 that DDT is stored in the body fat of mammals and appears in the milk. With this foreknowledge the series of catastrophic events that followed the most intensive campaign of mass poisoning in known human history, should not have surprised the experts. Yet, far from admitting a causal relationship so obvious that in any other field of biology it would be instantly accepted, virtually the entire apparatus of communication, lay and scientific alike, has been devoted to denying, concealing, suppressing, distorting and attempts to convert into its opposite, the overwhelming evidence. Libel, slander and economic boycott have not been overlooked in this campaign. 
[...]
Early in 1949, as a result of studies during the previous year, the author published reports implicating DDT preparations in the syndrome widely attributed to a "virus-X" in man, in "X-disease" in cattle and in often fatal syndromes in dogs and cats. The relationship was promptly denied by government officials, who provided no evidence to contest the author's observations but relied solely on the prestige of government authority and sheer numbers of experts to bolster their position.
[...]
["X-disease"] ...studied by the author following known exposure to DDT and related compounds and over and over again in the same patients, each time following known exposure. We have described the syndrome as follows: 
...In acute exacerbations, mild clonic convulsions involving mainly the legs, have been observed. Several young children exposed to DDT developed a limp lasting from 2 or 3 days to a week or more. 
[...]
Simultaneously with the occurrence of this disorder [X-disease] a number of related changes occurred in the incidence of known diseases. The most striking of these is poliomyelitis. In the United States the incidence of polio had been increasing prior to 1945 at a fairly constant rate, but its epidemiologic characteristics remained unchanged. Beginning in 1946 the rate of increase more than doubled. Since then remarkable changes in the character of the disease have been noted. Contrary to all past experience, the disease has remained epidemic year after year.
DDT vs Polio (1945-1953) 
In the graph below, I provide confirmation of Biskind's observations for 1945-1953, in terms of polio incidence and pesticide production. I have utilized pesticide data from Hayes and Laws which they had derived from US Tariff Commission data. Polio incidence data was gathered from US Vital Statistics.[3],[4] Although I argue herein against Hayes' characterization of Biskind's work, credit goes to Hayes for publishing arcane pesticide data. All graphs refer to paralytic polio.
Pesticides and Polio
Physiological Evidence 
Biskind also describes physiological evidence of DDT poisoning that resembles polio physiology: 
Particularly relevant to recent aspects of this problem are neglected studies by Lillie and his collaborators of the National Institutes of Health, published in 1944 and 1947 respectively, which showed that DDT may produce degeneration of the anterior horn cells of the spinal cord in animals. These changes do not occur regularly in exposed animals any more than they do in human beings, but they do appear often enough to be significant.
He continues, bearing his exasperation in trying to make the obvious plain. 
When the population is exposed to a chemical agent known to produce in animals lesions in the spinal cord resembling those in human polio, and thereafter the latter disease increases sharply in incidence and maintains its epidemic character year after year, is it unreasonable to suspect an etiologic relationship?
Before finding Biskind's work, I had spent months engaged in a nearly futile search for the physiology of acute DDT poisoning. I began to sense that American DDT literature as a whole intends to convey that DDT is not dangerous except with regard to its general environmental effects due to persistent bioaccumulation, and that the physiology of acute DDT poisoning is therefore trivial. DDT literature uniformly jumps from descriptions of symptoms, over physiology, to the biochemistry of DDT-caused dysfunction in nerve tissue. 
It was as though detectives had come upon a mass-murder scene and immediately became obsessed with the biochemistry of dying cells around bullet holes, while ignoring the bullet holes.
Eventually, I did find a German study of the physiology of acute DDT poisoning, by Daniel Dresden.[5] (Physiological Investigations Into The Action Of DDT, G.W. Van Der Wiel & Co., 1949) This study confirms that DDT poisoning often causes polio-like physiology: 
Conspicuous histological degeneration was, however, often found in the central nervous system. The most striking ones were found in the cerebellum, mainly in the nucleus dentatus and the cortex cells. Among other things an increase of the neuroglia and a necrotic degeneration and resorption of ganglionic cells was found. The Purkinje cells were less seriously affected than the other neurons. Also in the spinal cord abnormalities of a degenerative nature were found. 
...such changes were not found invariably... there is neither an obvious relation between the size and spreading of the lesion and the quantity of DDT applied... information of adequate precision about the nature of the anomalies is lacking. 
So we find that especially the cerebellum and the spinal cord are histologically affected by DDT.
And more recently, in the works of Ralph Scobey, MD, I found that from ancient times to the early 20th century, the symptoms and physiology of paralytic poliomyelitis were often described as the results of poisoning. It wasn't until the mid-19th century that the word "poliomyelitis" became the designation for the paralytic effects of both severe poisoning and polio-like diseases assumed to be germ-caused.[6]
In contemporary Britain, a farmer-turned-scientist, Mark Purdey, has found substantial evidence that Mad Cow Disease, a form of polio-like encephalitis, was caused by a government-mandated cattle treatment consisting of organophosphate pesticide and a compound similar to thalidomide.[7] Unlike most scientists, Mark Purdey became legally embroiled with the government during his research.[8]
Morton S. Biskind had the courage to write about humans. His views fell into disfavor after the introduction of the polio vaccines, which was a grand act that proved in most people's minds that polio was caused by a virus. By October, 1955, Biskind, whose works had been published in established medical journals and who testified before the Senate on the dangers of pesticides, was forced to self-publish his writings, one of which I found while browsing through an old card catalog. A scan of Medline/Pubmed[9] found no other works by him except for a very tame article in 1972, warning that diseases incurred during a patient's stay in a hospital are not necessarily due to microbes. He died not long thereafter, in his late 60s. I don't have the precise date of death, though his birth was in 1906.
A Contemporary Study 
Below are three graphs that confirm Biskind, utilizing data that spans far beyond his observations. Due to the paucity of data regarding pesticide exposure and locale, these findings of production data are presented as an indication of exposure, keeping in mind the great changes in public awareness and legislation beginning circa 1950, which also served to reduce DDT exposure. Pesticide production data comes from Hayes and Laws. 
DDT vs Polio (1940-1970) 
In this graph I did not include DDT data for the period of 1954 onward because DDT distribution was then being shifted out of the U.S. and into developing nations, while its U.S. production skyrocketed.
Governmental hearings, including those with Biskind, Scobey and others, brought about greater awareness of DDT dangers, as well as better labeling and handling methods.[10] Due to public governmental debate in 1949-51 and numerous policy and legislative changes afterward, DDT production figures after these dates do not correlate with US usage or exposure to DDT.[11],[12],[13]
Pesticides and Polio
DDT Before 1950
Before 1950, DDT was hailed as a miracle of progress that was virtually non-toxic to humans, in spite of FDA's warnings and attempts to keep it off the market. This photo on the left is one of several similar photos from Zimmerman, et al, DDT: Killer of Killers (1946). The advertisement on the right is from an unknown source, though it appears to be circa 1954.
Pesticides and Polio
Other photos in Zimmerman advocate 5% DDT solution sprayed directly on dairy cows (body, feed, and water):
Pesticides and Polio
DDT after 1950
Governmental hearings, including Biskind and Scobey, and others, eventually brought about greater awareness of the dangers, better labeling and handling methods.
DDT after 1954
This period is given special consideration for DDT.
After 1954, DDT production increased tremendously, but mainly as an export product. Due to public governmental debate in 1950-51 and numerous policy and legislative changes afterward, its production figures thereon do not at all correlate with U.S. usage or exposure to DDT.
As many studies demonstrate, DDT exposure after 1954 declined sharply, and this decline is represented in the following graph, along with supporting data. DDT production is not shown, post-1954.
Historical context: DDT was incriminated from 1950 until its registration cancelation in 1968 and ban in 1972. Thus, 1950-1951 represents a point of increased public awareness, changes in legislation and policy, voluntary phase-out, and labeling requirements. It is significant for this comparison of DDT against infantile paralysis, that before the period of increased awareness, DDT was mandated on dairies, yet afterward, ruled out of dairies. Much of the domestic usage was shifted to forestry applications, placing less DDT directly into the food chain.
The visual impact of all the persistent pesticide graphs rests upon the assumption that production correlated with human exposure. Given the lack of regulation and the extreme media hype surrounding DDT before 1953, this is not an unrealistic assumption.
It is clear that post-1954 DDT production did not correlate with human exposure. Yet, it is possible to estimate relative values for exposure post-1954. This can be accomplished by reviewing DDT levels in adipose tissue (National Adipose Tissue Survey, and other studies),[14] considering DDT in imported food, and considering the daily amounts of ingested DDT.
The early trend of National Adipose Tissue Survey's can be interpolated back to 1944, six years from 1950, the first Survey year, because it is safe to assume that DDT tissue levels were zero in 1944, since DDT was introduced for domestic usage in 1945. The estimate of DDT exposure is a reasonable because DDT has a half-life of about one year. To achieve any downward trend in the DDT/adipose line, DDT exposure had to have decreased sharply.
Note that no scale is provided for "relative DDT exposure". The Survey values are presented without distortion, linearly, with the starting point at 1954, and values for are estimates based on the Survey and DDT ingestion data. 
Error is limited by two boundaries, for the estimated values of DDT exposure. 1) Exposure's downward slope must be much greater than the Survey line's downward slope, because of DDT's half-life. 2) Exposure values must continue at least through 1968. 
Pesticides and Polio
Hayes and Laws also used a secondary evaluation, DDT intake per day, to explain that from 1954 to 1964-67, DDT ingestion decreased by an approximate factor of five. Significantly, the Salk vaccine program began in 1954.
The observed decrease in the concentration of DDT in food (Walker et al., 1954; Durham et al., 1965a; Duggan, 1968) offers an adequate reason for the decrease in storage in people. The average intake of p,p'-DDT and of total DDT-derived material was 0.178 and 0.280 mg/human/day, respectively, in 1954, but only 0.028 and 0.063 mg/human/day, respectively, during the period 1964-1967. (Hayes and Laws, page 303)
BHC vs Polio (1940-1970) 
BHC (benzene hexachloride), a persistent, organochlorine pesticide, is several times more lethal than DDT, in terms of LD50, i.e., the lethal dosage required to kill 50 percent of a test population.
Unlike the situation with DDT, in which there have been few recorded fatalities, there have been a number of fatalities following poisoning by the cyclodiene and hexachlorocyclohexane-type insecticides. The chlorinated cyclodiene insecticides are among the most toxic and environmentally persistent pesticides known." (Hayes & Laws)
As shown in the graph below, BHC was produced in 1945-1954 at quantities similar to DDT. In spite of BHC's lethal quality, it has received much less publicity than DDT. While DDT was banned for such things as an association with the thinning of eagles' eggs, BHC was phased out of production because it was found, after 15 years, to impart a bad taste to food. It is still used in developing nations. It is tempting to ask whether the highly public DDT was "fronting" for the more dangerous BHC. BHC's correlation with polio incidence is astonishing.
Pesticides and Polio
Lead-Arsenic vs. Polio (1940-1970)
After viewing the DDT and BHC graphs above, note that the period of 1940-46 is unaccounted for in terms of polio-pesticide correlation. The missing piece of the puzzle for this six-year period is supplied by the lead and arsenic compounds. These types of central nervous system ("CNS") poisons have been the central component of pesticides since their widespread use beginning approximately 1868 until the advent of the organochlorine pesticides in the early 1940s. For those who have thought that "organic" food was the norm before the release of DDT to the civilian sector in 1945, the immense production of lead-arsenic compounds presented in this graph is disappointing. This data requires a reconsideration of any perception regarding "natural" quantities of arsenic found in apple seeds, apricots, or almonds, where pesticides can accumulate systemically from contaminated earth.
Pesticides and Polio
Pesticide Composite: Summary
Just over three billion pounds of persistent pesticides are represented in the graph below. 
Virtually all peaks and valleys correlate with a direct one-to-one relationship with each pesticide as it enters and leaves the US market. Generally, pesticide production precedes polio incidence by 1 to 2 years. I assume that this variation is due to variations in reporting methods and the time it takes to move pesticides from factory to warehouse, through distribution channels, onto the food crops and to the dinner table. 
A composite of the three previous graphs, of the persistent pesticides -- lead, arsenic, and the dominant organochlorines (DDT and BHC) -- is represented in the following:
Pesticides and Polio
These four chemicals were not selected arbitrarily. These are representative of the major pesticides in use during the last major polio epidemic. They persist in the environment as neurotoxins that cause polio-like symptoms, polio-like physiology, and were dumped onto and into human food at dosage levels far above that approved by the FDA. They directly correlate with the incidence of various neurological diseases called "polio" before 1965. They were utilized, according to Biskind, in the "most intensive campaign of mass poisoning in known human history."
Virus Causation
A clear, direct, one-to-one relation between pesticides and paralytic polio over a period of 30 years with pesticides preceding polio incidence in the context of the CNS related physiology just described, leaves little room for complicated virus arguments, even as a co-factor, unless there exists a rigorous proof for virus causation. Polio shows no movement independent from pesticide movement as one would expect for the virus model. 
Medical propagandists promote images of a predatory, infectious virus, invading the body and quickly replicating to a level that causes disease, however, in the laboratory, poliovirus does not easily behave in such a predatory manner. Attempts to demonstrate virus causation are performed under extremely artificial and aberrant conditions.
Poliovirus causation was first established in the mainstream mind by publications of an experiment by Landsteiner and Popper in Germany, 1908-1909. Their method was to inject a purée of diseased tissue into two monkeys, "injected into the abdominal cavity". One monkey died after six days and the other was sickened.[15]
Proof of poliovirus causation was headlined by orthodoxy. This, however, was an assumption -- not a proof -- of virus causation. The weakness of this method is obvious to everyone except certain viropathologists and has recently been criticized by the molecular biologist Peter Duesberg regarding a modern-day attempt to establish virus causation for kuru, another CNS disease.[16]
Since 1908, the basic test, as intracranial injection, has been repeated successfully many times, using monkeys, dogs and genetically altered mice. However, a crucial weakness exists -- polio epidemics do not occur via injections of poliovirus isolate into the brains of the victims through a hole drilled in their skull -- except, of course, in laboratories and hospitals.
If injection into the brain is really a valid test for causation then it should serve especially well as a proof for pesticide causation. I propose that pesticides be injected directly into the brains of test animals. If paralysis and nerve degeneration subsequently occur, we then would have proved that pesticides cause polio.
Going further, towards much higher standards of proof than those used to prove virus causation, pesticides could be fed to animals and found to cause CNS disease. This has already been done with DDT and the histology of the spine and brain was poliomyelitis. Virus proofs require injection, often intracranial, to get any reaction from the experimental animal. It is axiomatic that a theory is only as good as its ability to predict future events. I predict that such a test would prove pesticides to be the most reliable causative factor.
The injection of purée of diseased brain tissue into the brains of dogs was the method preferred by Louis Pasteur to establish virus causation with rabies, another CNS disease. A recent, definitive biography of Pasteur finds him to be a most important publicist for germ theory, a crucial promoter for the notion that rabies is caused by a virus. Unfortunately, his rabies experiments were biased and unsupported by independent studies.[17] (G. L. Geison, The Private Science of Louis Pasteur, 1995)
Therefore, in my opinion, even a cofactor theory, where pesticides catalyze predatory poliovirus activity, or where pesticides weaken the immune system to allow opportunistic predatory poliovirus activity, cannot stand up to simple, common sense explanations that include the concept of a symbiotic virus. Neurotoxins are enough of a cause for neurological disease.
The most obvious theory -- pesticide causation -- should be the dominant theory. But the opposite exists, a pervasive silence regarding pesticide causation juxtaposed against a steady stream of drama regarding virus causation. In light of the evidence presented herein, the silence could ultimately discredit mainstream medical science, institutions of the environmental movement, and the World Health Organization (which directs both DDT application for mosquito campaigns and polio vaccination, world-wide).
Virus Presence
When the symptoms of polio are recognized, there is often a claim of virus presence in the body of the polio victim. Sometimes a virus is found. Sometimes that virus is an enterovirus (a virus of the digestive tract). Sometimes that enterovirus is a poliovirus. During polio epidemics, orthodoxy blames the poliovirus, and therefore, my argument for the innocence of the poliovirus requires an explanation of these claims of virus presence and the presence of an agent called the poliovirus. Here are three points:
a) Economic Impetus: During the great epidemic of 1942-1962 polio victims were diagnosed with poliovirus-caused polio, regardless of whether or not the poliovirus was found, because the NFIP (March of Dimes) funds paid only for this kind of polio. Therefore, if patients were going to spend time hospitalized, in iron lungs and undergoing therapy, it would have been economically imperative for the hospital to diagnose them in this way.[18] Thus, presence of poliovirus in poliomyelitis was rarely determined in order to arrive at a diagnosis of polio.
b) Other Pathogens: Even if one believes in virus culpability, other viruses are also claimed by orthodoxy to be the cause of polio-like CNS diseases which are "clinically indistinguishable" from polio. In the 1940-50s, relatively few polio victims were confirmed technically for presence of the poliovirus. In 1958, a laboratory analyses of 222 diagnosed polio victims (Detroit epidemic) found poliovirus in only 51% of the cases.[19] When multiple pathogens are hunted, a mix of pathogens, multiple viruses, fungi, and bacteria, can be associated with a single diagnosed case of polio.[20]
Coxsackievirus and echoviruses can cause paralytic syndromes that are clinically indistinguishable from paralytic poliomyelitis.[21] (John H. Menkes, Textbook Of Child Neurology, 5th ed., 1995, p420)
During a polio epidemic, such cases would have likely been diagnosed as "polio". After the 1970s, with the supposed approaching extinction of the poliovirus, such cases would have been diagnosed as encephalitis or meningitis.
c) Benign Virus: The poliovirus is considered to have been endemic throughout the world going back to ancient times, yet this is not the case with paralytic polio. According to Arno Karlen, author of Man and Microbes, the
polio virus lives only in people; it probably adapted to the human small intestine countless millennia ago." He continues, ". . . some historians have claimed that [paralytic] polio goes back to ancient Egypt; it may, but the evidence is thin."[22]
Karlen makes a lot of sense here in view of the pesticide graphs, Biskind's arguments, and ancient historians describing paralysis from the inhalation of vaporized chemicals during blacksmithing operations. However, Karlen goes on to write that "the first undisputed case dates from the late eighteenth century." This statement, however, must be invalid (in its attempt to establish polio images that have a basis in early history) because of Menkes' statement (above) that other viruses can also be causative for polio symptoms and because common industrial poisons such as arsenic and lead compounds can cause polio-like symptoms. Poisoning by arsenic, as a method of assassination, has also been frequently employed from the earliest eras, and it is not unreasonable to assume that unsuccessful poisonings would have left their victims paralyzed.
Orthodox medical literature can offer no evidence that the poliovirus was anything else than benign until the first polio epidemic, which occurred in Sweden in 1887. This small epidemic occurred 13 years after the invention of DDT in Germany, in 1874, and 14 years after the invention of the first mechanical pesticide crop sprayer, which was used to spray formulations of water, kerosene, soap and arsenic. The epidemic also occurred immediately following an unprecedented flurry of pesticide innovations. This is not to say that DDT was the actual cause of the first polio epidemic, as arsenic was then in widespread use, other organochlorines had been developed, and DDT is said to have been merely an academic exercise.
Poliovirus is categorized as an enterovirus. There are at least 72 known enteroviruses discovered to date. According to Duesberg, many enteroviruses are harmless "passenger viruses." In view of the material presented here, probably unknown to Duesberg, it is reasonable that we also view poliovirus as harmless outside of extreme laboratory conditions.
The Symbiotic Poliovirus 
Having now established the possibility of an innocent poliovirus, its presence in polio can be explained as follows, with five more points:
a) Accelerated Genetic Recombination: Genetic recombination is accelerated whenever a biological system is threatened.[23] Pesticides can be that threat. The proliferation of viruses is known to be part of the process of accelerated genetic recombination.
b) The SOS Response: When a cell is critically threatened, accelerated genetic recombination (which may include virus proliferation) is just one of a set of events that may occur. This set of events is called the "SOS response," which is known to be triggered by exposure to toxic chemicals or radiation.[24]
Arnold Levine, writing in Field's Virology, provides an example: 
When lysogenic bacteria were lysed [split open] from without, no virus was detected. But from time to time a bacterium spontaneously lysed and produced many viruses. The influence of ultraviolet light in inducing the release of these viruses was a key observation that began to outline this curious relation between a virus and its host."[25]
Is this mere irony? Common medical procedures such as chemotherapy, radiation therapy, and the use of toxic pharmaceuticals accelerate genetic recombination and thus the potential for a necessary virus proliferation.
c) The Ames Assay Test: The SOS response is utilized in the Ames Assay Test, a standard test whereby chemical toxicity is determined. According to the procedure, bacteria are exposed to a chemical solution in question, and if a genetic recombination accelerates via the spontaneous proliferation of viruses from these bacteria, then the chemical is determined to be a poison. The phenomenon is analogous to a poker player with a bad hand who must request an exchange of cards and a reshuffled deck to improve the possibilities for survival. In the Ames Assay Test, bacteria are concerned with their genetic "hand" in order to improve their abilities to metabolize poisons, create utilizations for poisons, and shield against poisons. Thus they engage in this well-known phenomena of "gene shuffling," facilitated by virus proliferation.
Thus, I propose that the poliovirus is a symbiotic (and possibly a dormant) virus that behaves in a manner suggested by the phenomenon found in the Ames Assay Test, a test used to determine toxicity.
One could object to this analogy on the grounds that because the Ames Test utilizes prokaryote cells (bacteria-like cells) rather than eukaryote cells (nucleus-containing cells that comprise multicellular tissue) and because it is asserted that poliovirus invokes damage by infecting eukaryote cells, the explanation is invalid. However, the evolution of eukaryotes includes structures and functions inherited from symbiotic unions of prokaryotes. Eukaryotes continue to possess to this day prokaryote functionality such as found in the genetic independence of the organelles within the eukaryote cells, such as mitochondria (Lynn Margulis and Dorion Sagan, What Is Life? (1995), and, Lynn Margulis, Dorion Sagan, Slanted Truths: Essays on Gaia, Symbiosis, and Evolution (1997)). Thus, generalizations derived from the Ames Test can contribute well to a valid hypothesis for the presence of poliovirus in "polio".
d) Dormant Virus: When a cell is critically threatened by toxic chemicals (or radiation) it can invoke survival mechanisms (the SOS Response) such as the suspension of metabolism, or the activation of dormant viruses, triggering their proliferation from the cell -- such viruses are said to be "dormant" or "latent". These words are not my preference because the way that they are popularly used implies that viruses are only externally generated and are found in the cell in a condition of temporary rest (dormancy). In cyclical phenomena, such as the life cycle of the virus, the "starting point" is a political-philosophical decision. The orthodox virus image (possibly a projection of the orthodox mind) is of an external, selfish, non-living parasite that tricks cells into infecting themselves with the virus and then to replicate said virus with cell machinery. Dormant viruses are publicized as external life forms that spend most of their time (as much as several decades) waiting inside cells, awaiting activation to perform parasitic activities. 
Recently it has become known that a tremendous amount of human DNA is devoted to virus proliferation. The virologist, Eleni Papadopulos-Eleopulos, stated in Continuum, Autumn 1997:
...it's accepted that endogenous retroviral DNA forms about 1% of human DNA... that's about 3,000 times larger than what the experts claim is the size of the HIV genome. And what's more, new retroviral genomes can arise by rearrangements and recombination of existing retroviral genomes.
Like the retroviruses, the poliovirus is an RNA virus and has a genome of similar weight and length. There is suspicion of dormant characteristics because enteroviruses have been found by several independent investigators, in post-polio (PMID: 8818905, UI: 96415998 (Lyon, France, Aug., 1996) and others).
e) Gene Sharing: Viruses represent shared capability, shared data, and data in transit. They are genetic couriers. Shared data decreases the burden on each cell to carry all capabilities. Capability, in the form of genetic information, can be stored in the environment as virus "gene packets", and different capabilities can be stored in different cells, just as humans each have, to some degree, uncommon capabilities which are shared with the community as needed. In the microbiotic world, when a specific capability is needed, cells share genetic information from the dynamically changing universal library of free floating genetic material, such as exists in viruses, free organelles, symbiotic parasites, and free nucleic acid, in addition to straight sexual intercourse where nucleic acid is transferred directly form cell to cell. It could be said that cells can carry dormant genetic information in the form of nucleic acid and when that information is required, share it through the proliferation of viruses. 
For example, in terms of disease, a symbiotic virus presence could be explained as a provider of cathartic capabilities or mechanisms, appropriate for various toxic or stressed environments. These cathartic mechanisms are manifested as disease symptoms, in the form of masses of sacrificed leucocytes, obviously found in boils, pimples, and pocks. Orthodoxy gives the label "transduction" to the processes of virus infection. Transduction is one of several modes of intercellular transport of genetic material, which allows for direct, laterally passed genetic data. Such data is routinely used to alter cell structure and metabolism modes dynamically, without engaging in the slower, more formal, sexual reproduction cycles. 
The concept of the symbiotic virus is explained in Encyclopedia Britannica, Macropaedia (1990) p507:
Although viruses were originally discovered and characterized because of the diseases they cause, most viruses that infect bacteria, plants, and animals (including humans) do not cause disease. In fact, bacteriophages [bacteria viruses] may be helpful in that they rapidly transfer genetic information from one bacterium to another, and viruses of plants and animals may convey genetic information among similar species, aiding the survival of their hosts in hostile environments.
Britannica continues with a praise of industrial biotechnology, and abruptly converts the probable-present into a future-made-possible by dependent consumers:
This could in the future be true for humans as well. Recombinant DNA biotechnology may allow genetic defects to be repaired by injecting afflicted persons with harmless viruses that carry and integrate functional genes to supplant defective ones.
The implication is that humans are not part of nature, however, in the next sentence Britannica states that we humans may already utilize symbiotic viruses:
Such events may actually occur in nature in the transmission of "good" viruses from one person to another.
The nature-friendly view, that viruses are effective genetic symbionts, dilutes the market impact of genetic-based treatments alluded to by Britannica, and threatens biotech profits. Perhaps this explains certain aspects of the current worldwide "war" against virus-carrying mosquitoes?
Virus Contradictions
The concept of a predatory poliovirus becomes less certain in the context of these little known virus "facts": 
1.
Poliovirus "[I]nfectosomes have yet to be experimentally demonstrated...", writes Roland R. Rueckert, under the subtitle, "Infection: A Rare Event" in Fields Virology.
2.
"Eukaryote cells have a wide arsenal of activities to control the half-lives of mRNAs, and these nucleases have made it difficult to isolate intact RNA viral genomes from cells." ("Virus Evolution", Ellen G. Strauss, et al, Fields Virology, Lippincott - Raven Publishers, Philadelphia (1996), v1p163)
In view of item 1, Rueckert, this appears to be another careful way of saying "never".
3.
The poliovirus does not always infect in accordance to its notoriety, "For every 200 or so virus particles that encounter a cell, only one will successfully enter and replicate, so research in this area is often confounded by the rarity of successful entry." (https://cumicro2.cpmc.columbia.edu/PICO/Chapters/Cellular.html (defunct link))
4.
Only herpesvirus has been traced enroute to site of disease from site of infection. "Viruses during retrograde transport on their way up to the cell bodies have so far been localized ultrastructurally only in the case of herpes simplex and herpes virus suis." (Martin E. Schwab and Hans Thoenen, Encyclopedia of Neuroscience, edited by George Adelman, pub, Birkhaüser Bros. Inc., Boston, 1987, Chapter 39, p102-3)
5.
A "poliovirus" has been electrophotographed in cell tissue. Due the lack of any photos of the virus as an infectosome, these photos should be interpreted as evidence of the cell's SOS response rather than of poliovirus causation. Electrophotography has existed for several decades and has yet to photograph a poliovirus infectosome. An infectosome is a "membrane-associated particle... which transfers genomic viral RNA through the membrane." (Field's Virology, 1996, p635)
6.
"It seems likely that all viruses trace their origins to cellular genes and can be considered as pieces of rogue nucleic acids." (Encyclopedia Britannica, Micropaedia, 1997, "Virus")
This demonstrates the great potential for a symbiotic relation between viruses and "hosts".
7.
The point in history when known viruses began their evolution has been calculated by molecular biochemists who have interpolated backwards through time the speed and direction of virus evolution. They found that "most viruses we know today have probably evolved since the last ice age." ("Virus Evolution", Ellen G. Strauss, et al, Fields Virology, 1996, p164)
8.
Viruses are involved in a process called transduction, one of the three modes of genetic transfer between cells, a process that can accelerate genetic recombination when cells are critically threatened by poisons.
9.
Virus infection is used by clone technology to transfer genetic material into cells.
10.
"Genetic information moves between viruses and their hosts to the point where definitions and classifications begin to blur." (Fields Virology, 1996, p6)
11.In terms of genetic similarity, "[T]here was a remarkable continuum..." from virus to host. (Fields Virology, 1996, p6)
12.
"Carrel (1926) was able to produce tumors resembling Rous' sarcoma and transmissible by cell-free filtrates with indol, arsenic, or tar in chicken embryo. Carrel's observations have been confirmed by other workers. Fischer (1926), by treating cultures of normal cells with arsenic obtained on one occasion a filtrable virus capable of causing tumors." (Ralph R. Scobey, M.D., "Poliomyelitis Caused by Exogenous Virus?", Science, v71, 1954)
Redefinition
Any of the items listed above can be used to direct work towards a refreshing view of viropathology. For instance, Alexis Carrel and Albert Fischer's experiments, in 1925-1926, preceded the discovery of the cellular SOS Response by decades. Their work is important in its impact on the basic tenants of viropathology, the contemporary proofs of virus causation, and definitions of immunity. Carrel, who happens to be one of the most recognized of all the Nobel Laureates, has stated without equivocation that the Rous sarcoma tumour is not infective, is caused by an agent within the cells themselves, yet is transmissible by cell-free Berkfeld filtrate of tumour extract. He states that the agent could not be a virus because of his assumption that a virus is an external, disease-causing, infectious entity. In retrospect such statements reveal the first (unrecognized) discovery of the dormant retrovirus. Carrel also clearly demonstrates poison causation for cancer. These landmark experiments are very simple, very clear, and totally ignored by orthodoxy. 
If one views Carrel and Fischer as a reinforcement of the symbiotic virus paradigm, then two strong alternative views can be defined regarding work that has been based on injections: 
Virus Disease: In the case of classical induction of disease by injection of extremely high quantities of virus, the alternative view would be that the presence of such quantities of virus serve as an informational context, a context that indicates imminent toxic death to naïve tissue, with an expected tissue reaction (disease). Or in other words, disease induction (via injection) is no more than an over-reaction (like jumping out of a window when someone yells "fire") in terms of inflammation and catharsis (disease manifestations).
Immunity: In the case of the classical demonstration of immunity whereby surviving subjects are found immune to attempts to induce disease by subsequent injections of virus, the alternative view is -- you can't fool them twice. 
Thus, a) inducement of disease by the injection of high-quantities of virus, and b) acquired immunity in survivors of these injections, can both be viewed as parlour tricks, though claimed to be demonstrations of virus causation for disease.
Conclusion
The word "virus" is ancient Latin, meaning "slime" or "poison". Mainstream science admits that most viruses are harmless, yet the word "virus" adds to a biased and highly promoted language of fear regarding nature. Definitions of viruses range from "pathogenic" to "not usually pathogenic" -- the more popular the media source, the more frightening the definition. Less fearful definitions would change the relationship between the medical industry and its "patients".
Paradoxically, early virus studies considered virus filtrates to be a poison, not a microbe, thus the name virus. Today, we know that viruses are information.
Now, nearly a half-century later, the validity of Dr. Biskind's work appears even more certain. Again, according to Biskind:
It was even known by 1945 that DDT is stored in the body fat of mammals and appears in the milk. With this foreknowledge the series of catastrophic events that followed the most intensive campaign of mass poisoning in known human history, should not have surprised the experts. Yet, far from admitting a causal relationship so obvious that in any other field of biology it would be instantly accepted, virtually the entire apparatus of communication, lay and scientific alike, has been devoted to denying, concealing, suppressing, distorting and attempts to convert into its opposite, the overwhelming evidence. Libel, slander and economic boycott have not been overlooked in this campaign.
The unique correlations between CNS disease and CNS poisons present a variety of research opportunities not only in medical science, but political science, philosophy, media studies, psychology, and sociology.[26],[27],[28],[29],[30],[31]
Author's note, 2015:
This article describes a view of polio, faithful to the tenets of the original article of June 2000. Research has continued through the present, however. For more information, an evolution of facts and concepts, books and articles, see https://harvoa.org
The intent herein is to provide an impartial, scholarly analysis of CNS disease and chemical causation. Current research priorities are for proof of poliovirus causation and/or proof that invalidates chemical causation.
Corrections, uncredited sources and/or copyright infractions, if any, will be rectified upon notice. This site is not a monologue of truth. It is a catalyst for the reevaluation of "polio". The reader is urged to confront officials to clarify issues mentioned herein.
This site is designed for critical, literary, and academic usage. A qualified and trustworthy medical professional must be consulted regarding medical issues, treatments, diagnoses, etc.

References
[1] 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.
[2] Morton S. Biskind, MD. "Public Health Aspects of the New Insecticides". American Journal of Digestive Diseases, New York, 1953, v 20, p331.
[3] U.S. Vital Statistics, U.S. Government Printing Office, Washington, D.C.
[4] Historical Statistics of the U.S., The U.S. Government Printing Office, Washington, D.C.
[5] Daniel Dresden, Physiological Investigations Into The Action Of DDT, G.W. Van Der Wiel & Co., Arnhem, 1949.
[6] Ralph R.Scobey, MD. "The Poison Cause of Poliomyelitis and Obstructions to Its Investigation." Archive of Pediatrics, April 1952.
[7] Mark Purdey's work can be found on the NIH website (PUBMED ID's 9572563, 8735882, 8735881) and in Wise Traditions, Spring 2000 and Spring 2002, Weston A. Price Foundation.
[8] WHALE, a medical criticism website, managed by John Scudamore. 
[10] Thomas R. Dunlap, DDT: Scientists, Citizens and Public Policy, Princeton University Press, 1981.
[11] Public Law 518, Federal Statutes, Volume 68, 1954, p 511.
[12] Public Law 905, Federal Statutes, 1956.
[13] "The Federal Insecticide, Fungicide and Rodenticide Act", Federal Statues, Volume 61, 1947, p 163.
[14] "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, p 303.
[15] The Landsteiner and Popper study, first published in Germany, was reported in an article by Robert W Lovett, MD., "The Occurrence of Infantile Paralysis in Massachusetts in 1908". Boston Medical and Surgical Journal, July 22, 1909, page 112.
[16] Peter Duesberg and Brian J. Ellison, Inventing the AIDS Virus, Regnery Pub., 1996.
[17] Gerald L. Geison, The Private Science Of Louis Pasteur, Princeton University Press, 1995.
[18] Julie Silver. "Three Signs of Post Polio Problems", Accent on Living, Winter 1995, v 40.
[19] Centers for Disease Control, Polio Packet, 1959.
[20] Richard T. Johnson, at the Department of Neurology, Johns Hopkins University School of Medicine, published in Annals of the New York Academy of Sciences, 1995 and excerpted in Jane Colby, ME: The New Plague, First and Best in Education, Ltd, 1996.
[21] John H. Menkes, Textbook Of Child Neurology, 5th ed., Williams & Wilkins, 1995, p 420.
[22] Arno Karlen, Man and Microbes, G.P. Putnum's Sons, 1995.
[23] Molecular Approaches to Environmental Biology, edited by Pickup, R.W and J.R. Saunders, Ellis Horwood publishers, 1996.
[24] Mark Ptashne, A Genetic Switch, Cell Press and Blackwell Scientific Publications, 50 Church St., Cambridge, MA 02138, 1992.
[25] Fields Virology, edited by B.N. Fields and others, Lippincott-Raven Publishers, Philadelphia, 1996, p 6.
[26] Aristotle, The Politics, Penguin Classics, Penguin Books (1962, reprinted 1992)
[27] Casarett and Doull's Toxicology, The Basic Science of Poisons, 5th ed., pub. McGraw-Hill (1996)
[28] Lynn Margulis, Dorion Sagan, Slanted Truths: Essays on Gaia, Symbiosis, and Evolution, Copernicus, New York (1997)
[29] Robert S. Mendelsohn, M.D., Confessions of a Medical Heretic, Contemporary Books, Chicago (1979)
[30] Robert Richter and Ruth Norris, Pills, Pesticides And Profits, North River Press, Inc. (1982)
[31] Jack Trombadore, "An Introduction to Post Polio Syndrome", New Jersey Polio Network Newsletter, Fall (1995)
Disclaimer: This article is not intended to provide medical advice, diagnosis or treatment. Views expressed here do not necessarily reflect those of GreenMedInfo or its staff.
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