Written by Abdun Nur
Polio is found only amongst humans and no other animals.
What factors excludes all other animals that generate toxin build up within the body?
- The filth and poverty orchestrated by a small group of humans inflicted on the majority of humans, causing them to suffer nutritional deficiencies, malnourishment, and environmental pollution which contaminates their water and food.
- A small group of humans impose chemical based mono-farming methods, lacing food production with poisons, pesticides and herbicides, while depleting the soils of nutrients and using chemical fertilisers, leaving food bereft of nutrition.
- A small group of humans deceptively inflicting vaccines (the injection of highly toxic poisons) onto and into the majority of humans.
In the early nineteenth century Polio was known variously as: Dental Paralysis, Infantile Spinal Paralysis, Essential Paralysis of Children, Regressive Paralysis, Myelitis of the Anterior Horns, Tephromyelitis (from the Greek tephros, meaning “ash-grey”) and Paralysis of the Morning. In 1789 the British physician Michael Underwood provided the first clinical description of poliomyelitis.
Polio mainly affects children younger than 5, claimed risk factors for polio, immunocompromisation and malnutrition.
Before 1800 Polio did not exist, up to the 19th century, populations experienced only relatively small outbreaks. This changed around the beginning of the 20th century with the increase in vaccinations. Major epidemics occurred in Norway and Sweden around 1905 and later also in the United States.
Several studies show that injections massively increase susceptibility to polio. When diphtheria and pertussis vaccines were introduced in the 1940s, cases of paralytic polio- myelitis skyrocketed. Source: National Morbidity Reports taken from U.S. Public Health surveillance reports; Lancet (April 18, 1950), pp. 659-63.
In 1949, the Medical Research Council in Great Britain set up a committee to investigate the matter and ultimately concluded that individuals are at increased risk of paralysis for 30 days following injections; injections alter the distribution of paralysis; and it did not matter whether the injections were subcutaneous or intramuscular.
The majority of infections (72%) according to the medical institutions do not lead to any symptoms. another way to say this is 72% of recorded cases do not have polio at all. About a quarter of cases (24%) result in “abortive” poliomyelitis which leads to nonspecific symptoms for a few days, such as a fever or a cold, and 1-5% of cases lead to “non-paralytic aseptic meningitis”, in which the patient suffers from stiff limbs for up to 10 day. 99.5% of cases resulting in only temporary symptoms.
The mechanisms by which polio spreads to the Central Nervous System are unknown to allopathic medicine.
Polio (toxins) destroys motor neurons within the grey matter of the spinal cord, brain stem, or motor cortex. This leads to the development of paralytic poliomyelitis, the various forms of which (spinal, bulbar, and bulbospinal) vary only with (level of toxin present) the amount of neuronal damage and inflammation that occurs, and the region of the central nervous system affected. Severe infection can extend into the brainstem and even higher structures, resulting in polioencephalitis, creating an inability to breathe, requiring mechanical assistance such as an iron lung.
From 1905 to 1962 Sweden had one of the world’s highest Polio incidence rates. Polio was not reported in statistics until 1905 as Polio is not primarily a deadly disease and the majority suffering Polio survive. Out of the 51,000 cases reported, between 1905-1962, there were 6,000 registered deaths demonstrating an 11.76% mortality rate on reported cases.
Sweden had a population of 5,294,885 in 1905 to 7,581,148 in 1962 the median population 6,438,016 over 57 years is 895 reported cases annually with 105 deaths, the odds of dying from polio were 1 in 61,314 and the odds of suffering polio were 1 in 7,193 annually.
The global incidence of Polio is claimed to have decreased by over 99% from the height of recorded cases, this is due to rebranding, this is a common method of the medical Mafia to claim a disease is gone, or reduced, simply by renaming the disease as something else, or changing how data is recorded.
The illness Polio is not caused by a virus, as there is no such thing as a virus of any kind.
The symptoms of Polio include fever, headache, sore throat, and vomiting. Some victims develop neurological complications, including stiffness of the neck and back, weak muscles, pain in the joints, and paralysis of one or more limbs or respiratory muscles.
Allopathic medicine has no treatment to remove polio it simply manages the symptoms. Paralytic polio is rarely permanent. Usually there is a full recovery. Muscle power begins to return after several days and continues to improve during the next 12-24 months. A small percentage of cases will experience residual paralysis. In rare cases, respiratory paralysis of the muscles used to breathe can lead to death.
1952 Vaccine Initiated – Initiators Jonas Salk (1914 – 1995) – oral version by Albert Bruce Sabin (1906 – 1993)
Vaccine Ingredients: Source- Centre for Disease Control and Prevention – Epidemiology and Prevention of Vaccine-Preventable Diseases, 13th Edition – Appendix B-9
2-phenoxyethanol – is an alternative to thiomersal (mercury). It’s a germicidal and germistatic glycol ether, phenol ether, and aromatic alcohol.
Formaldehyde – is a Carcinogen and extremely toxic, small doses can cause damage to the liver, kidney, spleen, pancreas, brain, and central nervous system, in infants as little as 30ml in a 37% solution caused death, the vaccine contains 200mcg per dose.
Neomycin – Neomycin is an aminoglycoside antibiotic. Neomycin may cause permanent hearing loss, nerve damage, and severe kidney damage, factors that increase the risk of these side effects occurring include advanced age or dehydration. Severe allergic reactions in some.
Streptomycin – an antibiotic, the first aminoglycoside to be discovered, the first effective treatment for tuberculosis. It is derived from the actinobacterium Streptomyces griseus. May cause severe toxic nerve reactions, vision problems, trouble keeping your balance, certain brain problems, and hearing problems (eg, permanent hearing loss). The risk of hearing problems may be increased if you have kidney problems or already have hearing problems. It may be increased if you get high doses of streptomycin, or if you get it for a long time. The risk may also be increased in older people, infants, or people who are dehydrated.
Polymyxin B Sulphate – an antibiotic primarily used for resistant Gram-negative infections. It is derived from the bacterium Bacillus polymyxa. Common side effects Fever; pain at the injection sit, irritability, weakness, drowsiness, numbness in the arms or legs, or blurred vision. Severe allergic reactions in some.
Monkey kidney cells – rhesus monkey kidney cells are used to cultivate diseased and rotting flesh
Eagle MEM modified medium – a cell culture medium developed by Harry Eagle which contains – amino acids, salts (calcium chloride, potassium chloride, magnesium sulphate, sodium chloride, and monosodium phosphate), glucose, vitamins (folic acid, nicotinamide, riboflavin, B12)
Calf serum protein Eagle MEM modified medium – a cell culture medium developed by Harry Eagle
- Medium 199 – primary explants of mouse pancreatic epithelium, and rat lens tissues.
Jonas Salk began to use animals as hosts, in the race to develop a commercially viable polio vaccine. Salk and his peers concocted from a degenerate unscientific brew of ingredients, including the minced up spinal cord from a 9-year-old deceased human child, water, blood, flies, faeces, and human cell matter. This mixture was injected into the brains of over 17,000 monkeys, most of which died instantly or became paralysed.
Clearly taking pleasure from the great suffering of his victims the psychopathic Salk continued with his slaughter, eventually presenting the commercial version of the polio vaccine, developed in part from “the faeces of three healthy children in Cleveland.”
Ironically this psychopathic, infamous father of the polio vaccine just recently was exposed for his role in illegal, depraved experiments on mental patients. Link
In 1952, Jonas Salk falsely claimed to have combined three types of poliovirus grown in cultures made from monkey kidneys. Using formaldehyde, he claimed he was able to “kill” or inactivate the (fictional) viral matter so that, he claimed, it would trigger an anti- body response without causing the disease. That year he began his initial experiments on human subjects. In 1953, his contrived findings were published in the Journal of the American Medical Association. And in April of 1954 the nation’s first polio immunisation campaign, directed at school children, was launched. However, shortly thereafter hundreds of people contracted polio from Salk’s vaccine; many died. Apparently, his vaccine was not preventing anything, but causing it. (Okonek BM,etal. Development of polio vaccines. Access Excellence Clas- sic Collection, February 16, 2001
The vaccine was redeveloped, and by August 1955 over 4 million doses were administered in the United States. By 1959, nearly 100 other countries were using Salk’s depraved vaccine.
In 1957, Albert Sabin, a physician (quack) and microbiologist, claimed to have developed a live-virus (oral) vaccine against polio. Always keep in mind every claimed virus is a concocted fiction, no virus has ever been proven to exist.
He didn’t think Salk’s vaccine would be effective in preventing epidemics. He wanted his vaccine to simulate a real-life infection. This meant using an attenuated or weakened form of the live (imaginary) virus. He experimented with thousands of monkeys and chimpanzees before he claimed to have isolated a rare type of polio that would reproduce in the intestinal tract without penetrating the central nervous system. The initial human trials were conducted in foreign countries. In 1958, it was tested in the United States. And in 1963 Sabin’s oral “sugar-cube” vaccine became available for general use. (A Science Odyssey: People and Discoveries. Salk produces polio vaccine)
No independent clinical studies on these vaccines to prove they work as claimed; none. No study that includes Pharmacodynamics and pharmacokinetics exist nor any evidence of specific inoculating antibodies created through vaccination.
American national immunisation campaigns were initiated in the 1950s, the number of reported cases of polio following mass inoculations with the Salk’s vaccine was significantly greater than before mass inoculations, and may have more than doubled in the U.S. as a whole. For example, Vermont reported 15 cases of polio during the one-year report period ending August 30, 1954 (before mass inoculations), compared to 55 cases of polio during the one-year period ending August 30, 1955 (after mass inoculations) a 266% increase. Rhode Island reported 22 cases during the before inoculations period as compared to 122 cases during the after inoculations period, a 454% increase. In New Hampshire the figures increased from 38 to 129; in Connecticut they rose from 144 to 276; and in Massachusetts they swelled from 273 to 2027, a whopping 642% increase. Source: U.S. Government statistics
Doctors and scientists on the staff of the National Institutes of Health during the 1950s were well aware that the Salk vaccine was causing polio. Some frankly stated that it was “worthless as a preventive and dangerous to take. McBean E. The Poisoned Needle. Mokelumne Hill, California: Health Research, 195
Vaccine Data Fraud
The polio vaccine was licensed in the U.S. in 1954. From ‘50 thru ‘55, about 85% of the reported cases, or 30,000 per year, on average, were automatically eliminated by two radical changes the CDC made to the diagnostic parameters and labelling protocol of the disease as soon as the vaccine was licensed – 30,000 cases a year we were subsequently told were eliminated by the vaccine.
That success, held aloft as a banner of the industry, is an illusion. The CDC has an awesome power of control over public perception, sculpting it from behind closed doors in Atlanta, with the point of a pen.
Over the last sixty years in the U.S., more than a million cases of what would have been diagnosed as polio pre-vaccine – same symptoms – were given different labels.
“After vaccination was introduced, cases of aseptic meningitis were reported as a separate disease from polio, but such were counted as polio before the vaccine was introduced. The Ministry of Health admitted that the vaccine status of the individual is a guiding factor in diagnosis… If a person who is vaccinated contracts the disease, the disease is simply recorded under a different name… Those who contracted polio after the first inoculation were placed on the non-inoculated list… It’s obvious that this practice of screening statistics, apparently in order to suppress facts unfavourable to immunisation, invalidates most of the evidence brought forward by the supporters of immunisation.” Maurice Beddow Bayly, member of the Royal College of Surgeons, LRCP, wrote in 1934
“Presently , a community is considered to have an epidemic when it has 35 cases of polio per year per 100,000 population. Prior to the introduction of the Salk vaccine the National Foundation defined an epidemic as 20 or more cases of polio per year per 100,000 population. On this basis there were many epidemics throughout the United States yearly. The present higher rate has resulted in not a real, but a semantic elimination of epidemics.” (Ratner report)
In the 90s, “polio eradication initiatives” were implemented in India and Africa. The WHO quickly established the same diagnostic changes in those nations as were made in the U.S. in 1955. The result, as expected, was the announcement two years ago that India is now polio free. What the WHO so conveniently omitted was any mention of the skyrocketing incidence, in both nations, of acute flaccid paralysis, clinically identical to polio, and following in the wake of the use of the oral polio vaccine, abandoned fifteen years ago in the U.S. because it triggers Vaccine Associated Paralytic Polio:
“In 1976, Dr. Jonas Salk, creator of the killed-virus vaccine used in the 1950s, testified that the live-virus vaccine (used almost exclusively in the U.S. from the early 1960s to 2000) was the ‘principal if not sole cause’ of all reported polio cases in the U.S. since 1961” Washington Post, September 24, 1976.
U.S. federal health agencies admit the following two facts: Salk’s polio vaccine released for public use between 1955 and 1963 was contaminated with SV40; and SV40 has been proven to cause cancer in animals.
Allopathic medicine has no treatment to remove polio it simply manages the symptoms. Paralytic polio is rarely permanent. Usually there is a full recovery. Muscle power begins to return after several days and continues to improve during the next 12-24 months. A small percentage of cases will experience residual paralysis. In rare cases, paralysis of the muscles used to breathe can lead to death.
Treatment of symptoms mainly consists of putting the patient to bed and allowing the affected limbs to be completely relaxed. If breathing is affected, a respirator or iron lung can be used. Physical therapy may be required.
Reasonable Treatment for Polio
Polio is caused by toxic heavy metal mercury poisoning. Eradication: do not use, or reduce consumption of corporate chemical mono-farming foods and a total ban on all vaccines and the majority of (toxic) pharmaceuticals the majority of which have little to no medical benefit.
Chelation of the heavy metals out of the body using bentonite clay, along with supplementation of essential metals.
During the polio epidemics in the 40s and 50s in the U.S., one doctor, Fred Klenner, MD, cured every one of the sixty polio patients he treated, some of them paralysed, using massive injections of vitamin C. Astoundingly, after summarizing his work, his success, at the annual AMA meeting in 1949, Dr. Klenner received neither questions nor comment from his colleagues, and no mention of it was ever made to the American public. Link
High doses of L-Ascorbic acid (vitamin C), this must be consumed when first made as it has a half life of 30 minutes and vitamin C is completely lost 2 hours after mixing). Small 5g doses taken every few hours between meals, mixed in clean water with a quarter to half the amount of bicarbonate of soda, the dosage should be maintained just below bowel tolerance. Bowel tolerance is the point at which diarrhoea ensues.
Magnesium phosphate decreases nerve pain and promotes the regeneration of the peripheral nerve.
Vitamins B-1, B-6, and B-12 have been found to be especially beneficial for treating neuropathy. Vitamin B-1, also known as thiamine, helps to reduce pain and inflammation and vitamin B-6 preserves the covering on nerve endings.
A deficiency of vitamin D3 impairs nociceptor function, worsens nerve damage, and lowers the pain threshold.
So the simple solution to Polio is chelation, Vitamin C, Magnesium Phosphate, vitamin D3 and vitamins B1, B6 B12
I’m in no way a licensed medical quack, I have no training in allopathic stupidity, which is designed to cause disease, and mask the symptoms of disease (in this description of quackery, I will make a distinction, those who sew up injuries and set bones, and prescribe antibiotics on the rare occasions the cleaners of disease form a bloom, are excluded from the term quack, and are decent and honest in their endeavours for the most part). I do not murder people for a living, as do many licensed allopathic quacks, especially oncologists, organ harvesters, virologists and vaccinators, nor do I promote unsafe and detrimental practices of unscientific stupidity such as chemo-therapy and vaccination, this is the disclaimer, if you worship the allopathic medical religion, nothing I will write would change that moronic mind set, so this disclaimer would make no difference, and for those foolish enough to seek out allopathic quackery for anything other than traumatic physical injury, you have my sympathy, they will cause you no end of suffering if you allow them.