1977 (March) Jonas and Darrell Salk AGAIN warned... live virus vaccines produce the same disease.
IN 1976, 1977 THE CREATORS OF THOSE VACCINES THEMSELVES WARNED THAT LIVE VIRUS VACCINES CAUSE THE VERY DISEASE THAT THEY ARE SUPPOSED TO ERADICATE, AND YET, NOT UNTIL 2000 DID THE CDC STOP ADMINISTERING THE ORAL LIVE VIRUS DOSES!
THEY STOPPED ALLOWING ANYONE BUT THE CDC TO SAY WHAT THEY SAW IN PATIENTS WAS POLIO BECAUSE ALL DIAGNOSES OF THE DISEASE FOR OVER A DECADE NOW MUST COME ONLY FROM THE CDC!
THE NEW AND IMPROVED DISEASE WE ONCE CALLED POLIO IS NOW CALLED "ACUTE FLACCID PARALYSIS". AND IT HAS THE SAME SYMPTOMS AND SAME EFFECTS ON HUMANS AS POLIO...BECAUSE THAT'S WHAT IT IS!
OTHER NATIONS STILL DIAGNOSE THE ILLNESS CORRECTLY, BUT NOT IN AMERICA, NO SIR!
AMERICA HAS ERADICATED POLIO...BECAUSE (A) IT CHANGED THE CRITERIA FOR DIAGNOSIS AND (B) GAVE IT A NEW NAME AND (C) WON'T ALLOW PHYSICIANS TO DIAGNOSE THEIR OWN PATIENTS WHOM THEY KNOW HAVE POLIO.
JUST CHANGING DIAGNOSIS CRITERIA WIPED OUT 35,000 KNOWN CASES RIGHT HERE IN "POLIO FREE" AMERICA, INSTANTLY!
DOESN'T THAT TELL YOU ALL ANYONE NEEDS TO KNOW ABOUT THE REAL AGENDA BEHIND VACCINES?
Abstract
Polio (poliomyelitis) is a potentially dangerous viral ailment.
To combat this disease, researchers developed two polio vaccines (inactivated and live) grown in cultures made from monkey kidneys.
Beginning in the 1950s, these vaccines were administered to millions of people in the United States and throughout the world.
Officially, the polio vaccine is considered safe and effective, and has been credited with singularly reducing the incidence of this disease.
These tenets are not supported by the data.
A cancer-causing monkey virus–SV-40–was discovered in polio vaccines administered to millions of people.
SV-40 has been found in brain tumors, bone cancers, lung cancers
and leukemia.
SV-40 is transmitted through sexual intercourse, and from mother to child in the womb.
Monkeys that were used to make polio vaccines were infected with simian
immunodeficiency virus (SIV), a virus closely related to human
immunodeficiency virus (SIV), a virus closely related to human
immunodeficiency virus (HIV), the infectious agent associated with AIDS.
Some researchers question whether HIVs may simply be SIVs “residing in and adapting to a human host.”
Polio vaccines also contain calf serum, glycerol and other parts of the cow that may have been infected with bovine spongiform encephalopathy (BSE),
or mad cow disease, a fatal brain-wasting ailment that some researchers link to Cruetzfeldt-Jakob disease (CJD), its human equivalent.
or mad cow disease, a fatal brain-wasting ailment that some researchers link to Cruetzfeldt-Jakob disease (CJD), its human equivalent.
Current disease reduction techniques that emphasize short-term gains over long-term health consequences need to be reevaluated and discontinued while new and safer health paradigms are researched and implemented.
IT DIAGNOSES POLIO TODAY AS "ACUTE FLACCID PARALYSIS".
FROM THE NATIONAL INSTITUTE OF MEDICINE:
The term acute flaccid paralysis (AFP) is often used to describe a sudden onset, as might be found with polio.
AFP is the most common sign of acute polio, and used for surveillance during polio outbreaks.
Included in AFP's list are Poliomyelitis (Polio), Transverse myelitis, Guillain-Barré syndrome, enteroviral encephalopathy, traumatic neuritis,Reye's syndrome, etc.
An AFP Surveillance programme is conducted to increase case yield of poliomyelitis.
This includes collection of 2 stool samples within 14 days of onset of paralysis and identification of virus.
ALMOST AN ADMISSION THAT AFP IS INDEED SIMPLY POLIO REDEFINED,
FROM THE OXFORD JOURNAL:
"Differential Diagnosis of Acute Flaccid Paralysis and Its Role in PoliomyelitisSurveillance.
Because poliomyelitis is on the verge of eradication,
accurate surveillance for AFP must be intensified.
The global incidence rate of nonpolio AFP would be expected to
be 1 per 100,000 among children under 15 years of age
under conditions of optimal surveillance with complete case
ascertainment.
Achieving and maintaining this detection
rate is considered the most sensitive performance criterion
for any AFP surveillance system. "
READ THE FOLLOWING FROM THE CDC WEBSITE CAREFULLY...
"To eliminate the risk of vaccine-associated paralytic poliomyelitis (VAPP), as of January 1, 2000, OPV was no longer recommended for routine immunization in the United States.
However, OPV continues to be used in the countries where polio is endemic or the risk
of importation and transmission is high.
OPV is recommended for global polio eradication activities in polio-endemic countries due to its advantages over IPV
in providing intestinal immunity
and providing secondary spread of the vaccine to unprotected contacts."
LET THAT SINK IN...THEY ADMIT THE LIVE OPV VACCINE CAUSES POLIO...BUT IT'S OKAY TO GIVE IT TO THIRD WORLD AND OTHER NATIONS...TO HELP "PROVIDE SECONDARY SPREAD OF THE VACCINE TO UNPROTECTED CONTACTS"...???
AND THE RISKS, FROM EVEN THE "INACTIVATED VACCINE"?
"Polio vaccine side-effects : The vaccine used today has never been known to cause any serious problems, and most people don’t have any problems at all with it.
However, a vaccine, like any medicine,
could cause serious problems,
such as a severe allergic reaction
or even death. "
WHO (WORLD HEALTH ORGANIZATION) defines AFP syndrome as "characterised by rapid onset of weakness of an individual's extremities, often including weakness of the muscles of respiration and swallowing, progressing to maximum severity within 1-10 days. The term 'flaccid' indicates the absence of spasticity or other signs of disordered central nervous system (CNS) motor tracts such as hyperflexia, clonus, or extensor plantar responses" (World Health Organization 1993 WHO/MNH/EPI/93.3. Geneva)
HOW DOES "WHO" DEFINE POLIO?
"Initial symptoms of polio include fever, fatigue, headache, vomiting, stiffness in the neck, and pain in the limbs.
In a small proportion of cases, the disease causes paralysis, which is often permanent.
There is no cure for polio, it can only be prevented by immunization."
THAT "DIAGNOSIS CRITERIA" SURELY FAILS...THOSE 'SYMPTOMS' COULD APPLY TO INFLUENZA OR SEVERAL OTHER ILLNESSES.
AND THAT LAST SENTENCE IS A BLATANT LIE!
THE CURE FOR POLIO COULD NOT BE SIMPLER AND WAS WELL KNOWN HALF A CENTURY AGO!
by Andrew W. Saul
Assistant Editor, Journal of Orthomolecular Medicine
from J Orthomolecular Med, 2007. Vol 22, No 1, p 31-38.
“Some physicians would stand by and see their patient die rather than use ascorbic acid because in their finite minds it exists only as a vitamin.” (F. R. Klenner, MD)
The sound barrier was broken in 1947. The Korean War began in 1950.
In between was the polio epidemic of 1948-9, during which Dr. Frederick Robert Klenner cured every polio case he saw by using vitamin C.
VITAMIN C AGAINST POLIO
Claus W. Jungeblut (1) had the initial idea; William J. McCormick (2) was an early proponent of frequent gram-sized doses. But it was Frederick Robert Klenner who first gave polio patients tens of thousands of milligrams of vitamin C per day. He had been doing so since before D-Day.
“From 1943 through 1947,” writes Robert Landwehr (3), “Dr. Klenner reported successful treatment of 41 more cases of viral pneumonia using massive doses of vitamin C. From these cases he learned what dosage and route of administration - intravenously, intramuscularly, or orally - was best for each patient. Dr. Klenner gave these details in a February 1948 paper published in the Journal of Southern Medicine and Surgery entitled ‘Virus Pneumonia and Its Treatment with Vitamin C.’ (4) This article was the first of Dr. Klenner’s twenty-eight (through 1974) scientific publications.”
“When I first came across Klenner’s work on polio patients,” writes Thomas Levy, “I was absolutely amazed and even a bit overwhelmed at what I read. . . To know that polio had been easily cured and so many babies, children, and some adults still continued to die or survive to be permanently crippled by this virus was extremely difficult to accept. . . Even more incredibly, Klenner briefly presented a summarization of his work on polio at the Annual Session of the American Medical Association on June 10, 1949 in Atlantic City , New Jersey
‘It might be interesting to learn how poliomyelitis was treated in Reidsville , N.C.
In the past seven years, virus infections have been treated and cured in a period of seventy-two hours by the employment of massive frequent injections of ascorbic acid, or vitamin C.
I believe that if vitamin C in these massive doses - 6,000 to 20,000 mg in a twenty-four hour period - is given to these patients with poliomyelitis none will be paralyzed and there will be no further maiming or epidemics of poliomyelitis.’ Levy concludes: “The four doctors who commented after Klenner did not have anything to say about his assertions.” (5)
“When proper amounts are used, it will destroy all virus organisms,” he would say. “Don’t expect control of a virus with 100 to 400 mg of C.” (6)
Klenner administered ascorbate by injection, and, as Lendon H. Smith describes in great detail in the Clinical Guide to the Use of Vitamin C: The Clinical Experiences of Frederick R. Klenner, M.D., Klenner found that “the most effective route was intravenous, but the intramuscular route was satisfactory. He gave at least 350 mg per kilogram of body weight.” That quantity per day is a dose of 25,000-30,000 mg or so for an adult. Yet, Smith adds, “With 350 mg per kilogram of body weight every two hours, he could stop measles and dry up chicken pox.”
This is indeed a large amount of vitamin C. Such use exemplifies the modern orthomolecular physician. Klenner’s doses were enormous, flexible and symptom-driven. The sicker the patient, the higher the dose. Massive ascorbate treatment cured every one of 60 polio cases Klenner saw. He published his report in Southern Medicine and Surgery in July of 1949. (7) All patients were well in three days. None had any paralysis.
In a 1950 letter, Klenner wrote:
“Since my last communication, I have seen four new cases of poliomyelitis. All of these have completely recovered. Three cases were seen in the acute febrile stage and in each instance, using 65 mg per kg body weight (by injection) every two (to) four hours, recovery was spontaneous in 48 hours.” (8)
In 1951, “In an especially incredible case,” Levy says, “Klenner (9) described a five-year-old girl stricken with polio. This child had already been paralyzed in both her lower legs for over four days! The right leg was completely limp, and the left leg was determined to be 85% flaccid. Pain was noticed especially in the knee and lumbar areas. Four consulting physicians confirmed the diagnosis of polio. Other than massage, vitamin C was the only therapy initiated. After four days of vitamin C injections the child was again moving both legs, but with only very slow and deliberate movement. Klenner also noted that there was a “definite response” after only the first injection of vitamin C. The child was discharged from the hospital after four days, and 1,000 mg of oral vitamin C was continued every two hours with fruit juice for seven days. The child was walking about, although slowly, on the 11th day of treatment. By the 19th day of treatment there was a “complete return of sensory and motor function,” and no long-term impairment ever resulted. Vitamin C not only completely cured this case of polio, it completely reversed what would undoubtedly have been a devastating, crippling result for the remainder of this girl’s life.” (4) For such elegant results, in the days before widespread use of either antibiotics or vaccination, one may wonder why Klenner was not awarded the Nobel Prize for Medicine.
Although specializing in diseases of the chest, he continued to do general practice because of the opportunities it afforded for observations in medicine. His patients were as enthusiastic as he in playing ‘guinea pigs’ to study the action of ascorbic acid.” (11)
Klenner had hospital privileges at Reidsville’s Annie Penn Memorial Hospital
In a 1978 letter to Klenner, Irwin Stone writes that he thinks that “giving levels of ascorbate for long periods of time at the daily levels you recommend. . . is equivalent to creating a new human subspecies, ‘Homo sapiens ascorbicus’ . . . with unusual resistance to disease and stress and with a prolonged life span.” Stone adds, “I was sorry to hear that the book you intend to write is still only a gleam in your eye.” (13)
Although he never would publish a book on vitamin therapy, Dr. Klenner was a Fellow of the American College of Chest Physicians, the American College
Dr. Klenner’s immensely valuable work is his legacy.
Linus Pauling said, “The early papers by Dr. Fred R. Klenner provide much information about the use of large doses of vitamin C in preventing and treating many diseases.
These papers are still important.” (32)
Klenner is justly remembered as the doctor who was first to boldly assert that “Ascorbic acid is the safest and most valuable substance available to the physician” and that patients should be given “large doses of vitamin C in all pathological conditions while the physician ponders the diagnosis.”
Whether overshadowed by scandal or stubbornly ignored by the medical profession, high-dose ascorbate therapy is here to stay.
“I have used Dr. Klenner’s methods on hundreds of patients,” said Dr. Lendon H. Smith. “He is right.”
[NOTE: All references from the above article are listed below as "SAUL REFERENCES"]
NO SURPRISE IN AN AUSTRALIAN FINDING THAT POLIOVIRUSES (PLURAL) WERE FOUND IN FECAL SAMPLES OF PATIENTS DIAGNOSED WITH AFP.
[SEE: Kelly H, Brussen KA, Lawrence A, Elliot E, Pearn J, Thorley B (2006). "Polioviruses and other enteroviruses isolated from faecal samples of patients with acute flaccid paralysis in Australia, 1996-2004". Journal of paediatrics and child health 42 (6): 370–6.doi:10.1111/j.1440-1754.2006.00875.x. PMID 16737480.]
MOST PEOPLE SIMPLY TRUST THEIR DOCTORS, WHICH THEY SHOULD NOT DO, BUT, INSTEAD, SHOULD BE INFORMED BY THEIR OWN CAREFUL IN-DEPTH RESEARCH, AND, WHEN IN DOUBT AS TO TREATMENT, SEEK A SECOND,OR EVEN A THIRD OPINION.
I AM SERIOUS WHEN I SAY THAT MOST OF TODAY'S PATIENTS, IF TOLD BY THEIR DOCTOR THAT HE WILL HAVE TO DETACH THEIR HEAD AND REATTACH IT TO THEIR ANKLE TO ALLEVIATE, SAY, MIGRAINE, WOULD JUST SAY, "OKAY, IF THAT'S WHAT IT TAKES..."
HERE ARE A FEW THINGS YOU MAY NOT KNOW, FACTS, THINGS ANYONE CAN FIND IN A SHORT TIME, OR BY ASKING VERY 'POINTED' QUESTIONS AND DEMANDING HONEST AND COMPLETE ANSWERS...IN OTHER WORDS, SIMPLY MAKE THEM PROVE WHAT THEY SAY BEYOND A SHADOW OF A DOUBT!
The history of "pharmaceutical science" is largely a story of FAILURES, as well as successes. Numerous drugs over the decades have been approved and THEN found MORE dangerous than the condition being targeted, but only after hundreds of thousands of people were turned into GUINEA PIGS by the medical establishment.
In the case of vaccines, both the first human papilloma vaccine (Gardasil) and Paul Offit’s vaccine for rotavirus (Rotateq) were disasters.
Both were fast-tracked through the FDA and both failed to live up to their promises.
This scenario of fast tracking unsafe and poorly researched vaccines was certainly the case for one of the first polio vaccines in 1955.
In fact the polio vaccine received FDA approval and licensure AFTER JUST TWO HOURS OF 'REVIEW'!
It was the fastest approved drug in the FDA’s history.
It was the fastest approved drug in the FDA’s history.
What happened after that initial vaccination was a NIGHTMARE! From the Journal of the Royal Society of Medicine:
"Known as the Cutter Incident, because the vaccine was manufactured by Cutter Laboratories, within days of vaccination, 40,000 children of the 200,000 vaccinated were left with polio, 200 with severe paralysis and there were ten deaths!
Shortly thereafter the vaccine was quickly withdrawn from circulation and abandoned.
Paul Offit, paediatrician and vaccine advocate, profiles leading figures, notably Jonas Salk and Albert Sabin —brilliant, egotistical and flawed characters—pioneers in vaccine development and as scientific celebrities, and notorious for their bitter personal rivalry.Reviewing failures in the manufacturing and inspection processes, he exonerates Salk from blame and concludes that `the federal government, through its vaccine regulatory agency... was in the best position to avoid the Cutter tragedy'.
The Cutter incident led to the replacement of Salk's formaldehyde-treated vaccine with Sabin's attenuated strain. Though Sabin's vaccine had the advantages of being administered orally and of fostering wider `contact immunity', it could also be re-activated by passage through the gut, resulting in occasional cases of polio (still causing paralysis in six to eight children every year in the 1980s and 1990s, when a modified Salk vaccine was re-introduced).
Offit observes, `ironically, the Cutter incident—by creating the perception among scientists and the public that Salk's vaccine was dangerous —led in part to the development of a polio vaccine that was more dangerous'.
The National Vaccine Injury Compensation Program was introduced in 1986 to protect vaccine manufacturers from litigation on a scale that threatened the continuing production of vaccines.
Offit proposes that the option of suing vaccine manufacturers should be stopped
and that compensation should only be available through the official programme."
YES, YOU READ THAT RIGHT...VACCINE MANUFACTURERS CAN'T BE SUED, EVEN IF YOUR CHILD DROPS DEAD BEFORE THE NEEDLE LEAVES HIS/HER ARM!
BUT CUTTER WAS NOT THE ONLY ONE SELLING KNOWN CONTAMINATED VACCINES!
In the 1980s, numerous companies, including Bayer's Cutter Biologic division, produced unsafe blood products to treat hemophilia.
The pharmaceutical product—produced from blood from donors across the US—was contaminated with the HIV virus at a time when HIV could not be screened out. These problems led to lawsuits over the next twenty years.
The pharmaceutical product—produced from blood from donors across the US—was contaminated with the HIV virus at a time when HIV could not be screened out. These problems led to lawsuits over the next twenty years.
A recent German documentary called "Tödlicher Ausverkauf: Wie BAYER AIDS nach Asien importierte" (Deadly Sale: How Bayer imported AIDS into Asia) researched the Koate product for hemophiliacs sold by Bayer's Cutter division under full knowledge of its HIV contamination.
Cutter ex-manager Merill Boyce expressed the opinion that the company should be responsible and pay damages.
Another ex-manager John H Hink, who also had been on the team that marketed Koate to Asia, expressed regret in the documentary that management had REQUIRED that they sell old stock despite knowledge of HIV contamination.
ETHICS IN THE CREATION OF NEW DRUGS AND VACCINES?
NONE THAT ARE NOTICEABLE.
NONE THAT ARE NOTICEABLE.
THE CDC COVERS FOR THE VACCINE MANUFACTURERS
The CDC’s website still promulgates a blatant untruth... that the Salk vaccine was a modern medical success.
To the contrary, officials at the National Institutes of Health were convinced that the vaccine was contributing to a rise in polio and paralysis cases in the 1950s.
In 1957 Edward McBean documented in his book The Poisoned Needle that government officials stated the vaccine was “worthless as a preventive and dangerous to take.”
Some states such as Idaho where several people died after receiving the Salk vaccine, wanted to hold the vaccine makers legally liable.
SALK ADMITS THE TRUTH
Dr. Salk himself testified in 1976 that his live virus vaccine, which continued to be distributed in the US until 2000, was the “principal if not sole cause” of all polio cases in the US since 1961. However, after much lobbying and political leveraging, private industry seduced the US Public Health Service to proclaim the vaccine safe.[2] Although this occurred in the 1950s, this same private industry game plan to coerce and buy off government health agencies has become epidemic with practically every vaccine brought to market during the past 50 years.
Today, US authorities proudly claim the nation is polio-free. Medical authorities and advocates of mass vaccination raise the polio vaccine as an example of a vaccine that eradicated a virus and proof of the unfounded “herd immune theory”.
Dr. Suzanne Humphries, a nephrologist and one of today’s most outspoken medical critics against vaccines has documented thoroughly that polio’s disappearance was actually a game of smoke and mirrors.
[SEE: Humphries, S. “Smoke, Mirrors and the Disappearance of Polio,” International Medical Council on Vaccination. November 17, 2011]
[SEE: Humphries, S. “Smoke, Mirrors and the Disappearance of Polio,” International Medical Council on Vaccination. November 17, 2011]
By 1961, the polio vaccine should have been ruled a dismal failure and abandoned since more people were being paralyzed from the vaccines than wild poliovirus infection.
NEED PROOF?IT IS ABUNDANTLY OUT THERE!
Among some of the more alarming discoveries since the SV40 was found in Salk’s and Sabin’s vaccines and its carcinogenic footprint in millions of Americans today are:
- Loyola University Medical Center identified SV40 in 38% of bone cancer cases [6]
- 58% of mesothelioma cases, a life threatening lung cancer, had SV40 present
- A later analysis of a large national cancer database found mesotheliomas were 178% higher among those who received the polio vaccines
- A study published in Cancer Research found SV40 in 23 percent of blood samples taken and 45% of semen samples studied, thereby confirming that the monkey virus can be sexually transmitted.
- Osteosarcomas are 10 times higher in states where the polio vaccine contaminated with SV40 was most used, particularly throughout the Northeastern states
- Two 1988 studies published in the New England Journal of Medicine discovered that SV40 can be passed on to infants whose mother’s received the SV40 tainted vaccines. Those children later had a 13 times greater rate of brain tumors compared to children whose mothers did not receive the polio vaccines. This would also explain why these children's tumors contained the SV40 virus present, EVEN THOUGH THE CHILDREN THEMSELVES NEVER RECEIVED THE VACCINE!
[62 peer-reviewed studies confirming the presence of SV40 in a variety of human tissues and different carcinomas were available way back in 2001 that prove this beyond a doubt.].
There is a very large body of scientific literature detailing the catastrophic consequences of SV40 virus infection.
Although the killed polio vaccines administered in developed countries no longer contain the SV40 virus, the oral vaccine continues to be the vaccine of choice in POOR developing countries because its cost-effectiveness to manufacture. Safety is clearly not a priority of the drug companies, health agencies and bureaucratic organizations that push especially the ORAL vaccine on impoverished children.
After almost sixty years of silence and a federally sanctioned cover up, the CDC finally admitted several years ago that the Salk and Sabin vaccines indeed were contaminated with the carcinogenic SV40 monkey virus.
However, SV40 is not the only contaminate parents should be worried about. As with other vaccines, such as measles, mumps, influenza, smallpox and others, the viral component of the vaccine continues to be cultured in animal cell medium. This medium can contain monkey kidney cells, newborn calf serum, bovine extract and more recently clostridium tetani, the causative agent for tetanus infection.
All animal tissue mediums can carry known and unknown pathogenic viruses, bacterial genetic residues, and foreign DNA fragments that pose countless potential health risks.
Based on transcripts of CDC meetings on biological safety, the late medical investigative reporter, Janine Roberts, noted that vaccine makers and government health officials admit they have no way to prevent dangerous carcinogenic and autoimmune causative genetic material from being injected into an infant.
Among the unwanted genetic material that might be found in vaccines today are: cancer-causing oncogenes, bird leukemia virus, equine arthritic virus, prions (a protein responsible for Mad Cow Disease and other life threatening illnesses), enzyme reverse transcriptase (a biological marker associated with HIV infection), and a multitude of extraneous DNA fragments and contaminates that escape filtration during vaccine preparation.
[SEE: Gale, R. and Null, G. “Vaccines’ Dark Inferno: What Is Not on Insert Labels.” GlobalResearch. September 29, 2009.]
The CDC acknowledges that it is impossible to remove all foreign genetic and viral material from vaccines. As Janine Roberts noted, the science behind the manufacture of vaccines is extraordinarily primitive. Therefore, the CDC sets limits for how much genetic contamination by weight is permitted in a vaccine, and the agency over the years continues to increase the threshold. [Gale and Null, Ibid.]
Amidst the polio vaccine debacle and mounds of scientific literature confirming the vaccines’ failure, US health agencies and the most ardent proponents of vaccines, such as Paul Offit and Bill Gates, retreat into the protected cloisters of medical denialism and continue to spew folktales of polio vaccines’ success.
In recent years Bill Gates’ polio eradication campaigns in India have been dismal failures. Touted as one of the “most expensive public health campaigns in history” according to Bloomberg Business, as many as 15 doses of oral polio vaccine FAILED to immunize the poorest of Indian children.
Severe gastrointestinal damage due to contaminated water and wretched sanitation conditions have made the vaccine ineffective.
Similar cases have been reported with the rotavirus and cholera vaccine failures in Brazil, Peru and Bangladesh.
According to epidemiologist Nicholas Grassly at Imperial College London, “ There is increasing evidence that oral polio failure is the result of exposure to other gut infections.” [SEE: Narayan, A. “Extra Food Means Nothing to Stunted Kids with Bad Water Health,” Bloomberg Business. June 12, 2013]
There is another even more frightening consequence of Gates’ vaccine boondoggle launched upon rural India in 2011.
This particular polio vaccine contains an INCREASED dosage of the polio virus.
In the April-June 2012 issue of the Indian Journal of Medical Ethics, a paper reported the incidence of 47,500 new cases of what is being termed “non-polio acute flaccid paralysis”, or NPAFP, following Gates polio campaign.
[SEE: Vashisht, N. and Puliyel J. “Polio Program: Let Us Declare Victory and Move On,” Indian Journal of Medical Ethics.April-June 9:2, 2012 pp 114-117]
[SEE: Vashisht, N. and Puliyel J. “Polio Program: Let Us Declare Victory and Move On,” Indian Journal of Medical Ethics.April-June 9:2, 2012 pp 114-117]
The following year, there were over 53,500 reported cases.
NPAFP is clinically indistinguishable from wild polio paralysis as well as polio vaccine-induced paralysis. The primary difference is that NPAFP is far more fatal.[SEE: “53,000 Paralysis Cases in India from Polio Vaccine in a Year” Child Health Safety. December 1, 2014]
Physicians at New Delhi’s St. Stephen's Hospital analyzed national polio surveillance data and found direct links between the increased dosages of the polio vaccine and rise in NPAFP.
Coincidentally, the two states with the highest number of cases, Uttar Pradesh and Bihar, are also the two states with the worst water contamination, poverty and highest rates of gastrointestinal diseases reported by Bloomberg.
As early as 1948, during a particularly terrible polio outbreak in the US, Dr Benjamin Sandler at Oteen Veterans’ Hospital observed the relationship between polio infection, malnutrition and poor diets relying heavily on starches.
[Miller, N. op cit.]
According to nutrition data, white rice, the primary daily food staple among poorer Indians, has the highest starch content among all foods.
[Chandra RK. “Reduced secretory antibody response to live attenuated measles and poliovirus vaccines in malnourished children,” British Medical Journal 2, 1975, 583–5]
Despite this crisis, in January 2014, Bill Gates, the WHO and the Indian government announced India is today a polio-free nation.
[ Krishnan, V. “India to get polio-free status amid rise in acute flaccid paralysis cases,” Live Mint (India), January 13, 2014.]
Another sleight of hand performance of the polio vaccine’s magic act.
Many historians of science, such as Robert Johnson at the University of Illinois, agree that the decrease in polio and other infectious diseases during the first half of the twentieth century were largely the result of concerted national public health efforts to improve sanitation and public water systems, crowded factory conditions, better hygienic food processing, and new advances in medicine and health care. Relying upon the unfounded myth that vaccines are a magic bullet to protect a population suffering from extreme conditions of poverty, while failing to improve these populations’ living standards, is a no-win scenario.
Vaccines will continue to fail and further endanger the millions of children’s health with severely impaired immune systems with high levels of vaccines’ infectious agents and other toxic ingredients.
Last year, researchers at the University of Bonn isolated a new strain of poliovirus that evades vaccine protection.
During a 2010 polio outbreak in a VACCINATED region of the Congo, there were 445 cases of polio paralysis and 209 deaths.
[Malory, M. “Mutant poliovirus caused Republic of Congo outbreak in 2010,” Medical Xpress. August 19, 2014]
This is only the most recent report of poliovirus strains’ mutation that calls the entire medical edifice of the vaccine’s efficacy into question.
One of the first discoveries of the vaccine contributing to the rise of new polio strains was reported by the Institut Pasteur in 1993.
Dr. Crainic at the Institut proved that if you vaccinate a person with 3 strains of poliovirus, a fourth strain will emerge and therefore the vaccine itself is contributing to recombinant activity between strains.
Since the poliovirus is excreted through a person's GI system, it is commonly present in sewage and then in water sources. In 200, Japanese scientists discovered a new infectious polio strain in rivers and sewage near Tokyo. After genetic sequencing, the novel mutation was able to be traced back to the polio vaccine. Additional vaccine-derived polio strains have also been identified in Egypt, Haiti and the Dominican Republic.
[ Miller, N. op cit.]
Therefore, the emergence of new polio strains due to over-vaccination is predictable.
Similar developments are being discovered with a new PERTUSSIS strain that evades the current DPT vaccines.
For this reason, there has been an increase in whooping cough outbreaks among fully vaccinated children.
Influenza viruses regularly mutate and evade current flu vaccines.
The measles vaccine is becoming less and less effective, and again measles outbreaks are occurring among some of the most highly vaccinated populations.
As with the failure of antibiotics because of their over-reliance to fight infections, researchers are now more readily willing to entertain the likelihood that massive vaccination campaigns are contributing to the emergence of new, more deadly viral strains impervious to current vaccines.
NO ONE REALLY UNDERSTANDS VIRUSES!
THEY ARE INCREDIBLY AND MADDENINGLY ADAPTIVE.
KILL THEM WITH ONE THING, THEY MUTATE AND BECOME IMMUNE TO THAT, AND OFTEN, IN SO DOING, BECOME EVEN WORSE THAN BEFORE.
WE WERE BETTER OFF, I THINK, WITH THE ORIGINAL STRAINS, BUT THERE'S NO GOING BACK NOW.
THEY REMIND ME A BIT OF THE "BORG" IN THE SERIES "STAR TREK"...
AND RESISTANCE JUST VERY WELL MAY BE, INDEED, FUTILE.
WE HAVE ALL THIS NEW KNOWLEDGE...TO IGNORE IT, TO GO ON REPEATING THE SAME ERROR OVER AND OVER AGAIN, IGNORING THE FACTS, RENAMING DISEASES TO HIDE THEM IS NO SOLUTION, BUT IS A SIGN OF INSANITY!
NO ONE REALLY UNDERSTANDS VIRUSES!
THEY ARE INCREDIBLY AND MADDENINGLY ADAPTIVE.
KILL THEM WITH ONE THING, THEY MUTATE AND BECOME IMMUNE TO THAT, AND OFTEN, IN SO DOING, BECOME EVEN WORSE THAN BEFORE.
WE WERE BETTER OFF, I THINK, WITH THE ORIGINAL STRAINS, BUT THERE'S NO GOING BACK NOW.
THEY REMIND ME A BIT OF THE "BORG" IN THE SERIES "STAR TREK"...
AND RESISTANCE JUST VERY WELL MAY BE, INDEED, FUTILE.
WE HAVE ALL THIS NEW KNOWLEDGE...TO IGNORE IT, TO GO ON REPEATING THE SAME ERROR OVER AND OVER AGAIN, IGNORING THE FACTS, RENAMING DISEASES TO HIDE THEM IS NO SOLUTION, BUT IS A SIGN OF INSANITY!
WITH KNOWLEDGE AND DETERMINATION, IF WE APPLY FACTS AND PURE TRUTH, IF WE STOP IGNORING AND PRETENDING ALL IS WELL, WE CAN ACCOMPLISH THINGS PREVIOUSLY DEEMED IMPOSSIBLE
THE POLIO VACCINE AS A CURE IS A HOAX...NOW FOR FINDING A REAL CURE...WHICH HAS ALREADY BEEN FOUND!
BUT MEASURES MUST BE TAKEN TO PREVENT A CHILD CONTRACTING POLIO.
THAT IS WHAT WE STILL MUST WORK ON!
SOURCES AND FURTHER
~ Miller, N. “The polio vaccine: a critical assessment of its arcane history, efficacy, and long-term health-related consequences” Medical Veritas. Vol. 1 239-251, 2004
~ McBean E. The Poisoned Needle. Mokelumne Hill, California: Health Research,1957
~ Lancet, March 9, 2002
~ Mihalovic, D. “CDC Admits 98 Million Americans Received Polio Vaccine in an 8 Year Span When It Was Contaminated with Cancer Virus.” Prevent Disease, July 17, 2013
"SAUL REFERENCES"
References:
1. Saul AW. Claus Washington Jungeblut, M.D.: Polio pioneer; ascorbate advocate. J Orthomolecular Med, 2006. Vol 21, No 2, p 102-106. http://www.doctoryourself.com/jungeblut.html
2. Saul AW. The pioneering work of William J. McCormick, M.D.. J Orthomolecular Med, 2003. Vol 18, No 2, p 93-96.http://www.doctoryourself.com/mccormick.html
3. Landwehr R. The origin of the 42-year stonewall of vitamin C. J Orthomolecular Med, 1991. Vol 6, No 2, p 99-103.http://www.whale.to/v/c/index.html
4. Klenner FR. Virus pneumonia and its treatment with vitamin C. Southern Medicine and Surgery, 1948, February. Vol 110, No 2, p 36-38, 46. http://www.whale.to/v/c/index.html"
5. Levy TE. Vitamin C, infectious diseases, and toxins: Curing the incurable. Philadelphia , PA
6. Smith, LH. Clinical guide to the use of vitamin C: The clinical experiences of Frederick R. Klenner, M.D.. Portland , OR
7. Klenner FR. The treatment of poliomyelitis and other virus diseases with vitamin C. South Med J, 1949, July. 3(7), p 209-214.http://www.orthomed.com/polio.htm and http://www.whale.to/v/c/index.html"
8. Klenner FR. Letter to M.G. Farnsworth, Farnsworth Laboratories, Inc., Chicago
9. Klenner FR. Massive doses of vitamin C and the virus diseases. South Med J. 1951 Apr;113(4):101-7. PMID: 14855098
10. Bledsoe J. Bitter blood: A true story of Southern family pride, madness, and multiple murder. NY: Dutton, 1988. Also: NY: New American Library, 1989. Page 114.
11. Klenner FR. Observations on the dose of administration of ascorbic acid when employed beyond the range of a vitamin in human pathology. J Applied Nutrition, 1971, Winter. Vol 23, No 3 and 4, p 61-68. http://www.orthomed.com/klenner.htm andhttp://www.doctoryourself.com/klennerpaper.html
12. Stone I. The healing factor: Vitamin C against disease. NY: Grosset and Dunlap, 1972; p 191-192.
13. Letter from Irwin Stone to Dr. & Mrs. Frederick R. Klenner, Gilmer Street , Reidsville , North Carolina Greensboro , NC , about four miles west of US Highway 29, and five blocks north of the Annie Penn Memorial Hospital
14. Saul AW. The 2005 Orthomolecular Medicine Hall of Fame. J Orthomolecular Med, 2005. Vol 20, No 2, p 113- 117. http://orthomolecular.org/hof/index.shtml
15. Miller F. Klenner’s office recalls old-fashioned practitioner. Greensboro Daily News, undated reprint. This medium-circulation newspaper, founded in 1909, has been known since 1982 as the News-Record. The periodical’s archives are accessible at
16. Bledsoe J, p 231.
17. Miller F. Dr. Klenner urges taking vitamins in huge doses. Greensboro
18. Klenner FR. A new office procedure for the determination of plasma levels for ascorbic acid. Tri-State Medical J, 1956, February, p 26-28.
19. Klenner FR. The history of lockjaw. Tri-State Med J, 1954, June.
20. Klenner FR. Recent discoveries in the treatment of lockjaw with vitamin C and tolserol. Tri-State Med J, 1954, July.
21. Klenner FR. A treatment of trichinosis with massive doses of vitamin C and
para-aminobenzoic acid. Tri-State Medical J, 1954, April.
22. Klenner FR. Case history: The black widow spider. Tri-State Med J, 1957, December.
23. Klenner FR. Case history: Cure of a 4-year old child bitten by a mature Highland Moccasin with vitamin C. Tri-State Med J, 1954, July. The Highland Moccasin, a viper, is also known as the copperhead.
24. Sern EL. The intraspinal injection of vitamin B-1 for the relief of intractable pain, and for inflammatory and degenerative diseases of the central nervous system. Amer J Surg, 1938. 34:495.
25. Moore MT. Treatment of multiple sclerosis with nicotinic acid and vitamin B-1. Archives Int Med, 1940, January, Vol 65, p 18.
26. Zimmerman HH, Burack F. Lesions of the nervous system resulting from a deficiency of the vitamin B complex. Arch Pathology, 1932, February, Vol 13:207.
27. Klenner FR. Response of peripheral and central nerve pathology to mega-doses of the vitamin B-complex and other metabolites. Parts 1 and 2. J Applied Nutrition, 1973, 25:16-40.
[Free full text download at http://www.townsendletter.com/Klenner/KlennerProtocol_forMS.pdf
Also: Klenner, FR. Treating multiple sclerosis nutritionally. Cancer Control J, undated. 2:3, p 16-20. And, a similar, comprehensive MS/MG protocol is to be found in the Clinical Guide to the Use of Vitamin C: The Clinical Experiences of Frederick R. Klenner, M.D., reference 6, above.]
[Free full text download at http://www.townsendletter.com/Klenner/KlennerProtocol_forMS.pdf
Also: Klenner, FR. Treating multiple sclerosis nutritionally. Cancer Control J, undated. 2:3, p 16-20. And, a similar, comprehensive MS/MG protocol is to be found in the Clinical Guide to the Use of Vitamin C: The Clinical Experiences of Frederick R. Klenner, M.D., reference 6, above.]
28. Program prescribed by Dr. Fred R. Klenner, a two-page itemized check-off list of nutritional recommendations for patients. Hand-dated January 25, 1979 by Irwin Stone, who added a notation that it had been “Rec’d from L. P. Institute.” (Linus Pauling Institute of Science and Medicine). Provided by Steve Stone.
32. Pauling L. Foreword to: Stone I. Clinical guide to the use of vitamin C: The clinical experiences of Frederick R. Klenner, M.D..
For further reading:
Klenner FR. Massive doses of vitamin C and the virus diseases. South Med J, 1951, Apr;113(4):101-7. PMID: 14855098. Sometimes erroneously cited as 103(4), such as in this link, which does in fact access the full text of the paper:
Klenner FR. The vitamin and massage treatment for acute poliomyelitis. South Med J, 1952, Aug;114(8):194-7. PMID: 12984224
The US National Library of Medicine, the world’s largest medical library, indexes nothing whatsoever written by Klenner after 1952.
