Schweinerei mit der Schweinegrippe.

Die Weltgesundheitsorganisation empfiehlt seinen 194 Mitgliedsländern Zwangsimpfungen gegen die Schweinegrippe.
Laut einer Reportage der Journalistin Jane Burgermeister wurde am 13. Juli von einem Beratungsgremium der Weltgesundheitsorganisation (WHO) die Empfehlung ausgesprochen, alle Menschen in den 194 Mitgliedsstaaten der WHO einer Zwangsimpfung gegen die Schweinegrippe zu unterziehen. Dem Beratungsgremium zugehörig sind Vorstände und Führungskräfte der Pharma-Riesen Baxter, Novatis, Glaxo-Smith Kline und Sanofi Pasteur. Dass diese die Impfstoffe liefern, ist natürlich reiner Zufall und hat mit der Empfehlung gar nichts zu tun.
Als eine der ersten Nationen, die dieser Empfehlung folgen, bereitet sich zur Zeit die Schweiz auf die Zwangsimpfungen vor.
Für jeden Bewohner der Schweiz sind zwei Impfdosen vorgesehen, wenn ab Herbst die Zwangsimpfung der Bevölkerung gegen Schweingrippe vollzogen wird. Die ersten 1,6 Millionen von den insgesamt bestellten 13 Millionen Spritzen sind eingetroffen.
Auf die Impfung bereiten sich zurzeit auch die Kantone vor. Sie bestimmen, wo Impfzentren eingerichtet werden und wer beim Impfen zuerst an die Reihe kommt. Jeder Bewohner der Schweiz wird dann laut Einwohnerregister eine schriftliche Aufforderung erhalten, wo und wann man für eine Impfung zu erscheinen hat.
Was die Behörden bewusst noch nicht verkündet haben, wie werden sie gegen die Personen vorgehen, die sich weigern dem Impfzwang zu folgen? Ein mögliche Maßnahme ist die Quarantäne, also die völlige Isolierung der Verweigerer vor der Außenwelt, entweder zu Hause, in Sammelquartiere oder in Lager.
Eingekauft wurden die Impfstoffe im Auftrag des Bundesamtes für Gesundheit (BAG). Grundlage ist der Pandemieplan. Die 13 Millionen Dosen Impfstoff gegen das H1N1-Virus für die Schweiz wurden bestellt bei zwei Herstellern, Glaxo SmithKline und Novartis, die im Herbst eintreffen und 84 Millionen Franken kosten.
Im Impfstoff ist Thimerosal enthalten, ein auf Quecksilber basierender Konservierungsstoff. Das Quecksilber darin ist nachweislich für den starken Anstieg um 1.500 Prozent von Autismus bei Kindern verantwortlich, seit dem Kleinkinder grundsätzlich geimpft werden. Russland hat deshalb bereits seit 1980 Thimerosal verboten. Das Schweizer Bundesamte für Gesundheit schreibt dazu auf ihrer Webseite "Keine Impfung ist ganz ohne Risiko".
Im September kommt der Stoff und wird gleich in die gesamte Bevölkerung rein geschossen - ohne vorher auf Sicherheit zu prüfen! Und ohne einen wirklichen Grund einer Gesundheitsgefährdung zu haben, denn Schweinegrippe ist gleich oder sogar harmloser als die normale Influenza.
So sterben jährlich zirka eine halbe Million Menschen an der ganz normalen Grippe. An der Schweinegrippe sind bislang wie viele gestorben? 800? 900?
Ne, ist klar.

British Nurses refusing Swineflu vaccine.
One third of NHS nurses in UK refuse to take shot, citing safety fears over vaccine’s link with Guillain-Barre Syndrome, autism and neurological disorders. The nationwide revolt against government plans to implement a mass swine flu vaccination program in the United Kingdom has picked up steam, with a poll revealing that a third of NHS nurses will refuse to take the shot.
Despite nurses and frontline health workers being the primary target group to take the vaccine, just 37 per cent of them said they would take the swine flu vaccine in a survey conducted by Nursing Times magazine. 30 per cent said they would not be immunized and 33 per cent said they were unsure.
Of the 30 per cent who said they would refuse to be vaccinated, 60 per cent said the reason was due to fears about the safety of the vaccine, following revelations that the shots will contain mercury and squalene and have also been linked with the killer nerve disease Guillain-Barre Syndrome. Another 31 per cent said they would refuse the vaccine because they did not consider the risk from swine flu to be great enough.
The government responded to the poll by claiming that nurses have a duty not to infect their patients and urged them to take the vaccine, but it seems that many fear the health consequences of taking the vaccine will be worse than catching the virus itself.
Interestingly, a London Times article on the story reveals that fewer than one in seven nurses in the UK receives the annual flu shot, highlighting the fact that health workers, who would be in a position to be well educated on the issue, are already fully aware of the dangers associated with vaccines in general.
The swine flu vaccine is being rushed through safety procedures while the government has provided pharmaceutical companies with blanket immunity from lawsuits arriving out of the vaccine causing deaths and injuries.
It was previously revealed that some batches of the vaccine will contain mercury, a toxin linked with autism and neurological disorders. The vaccine will also contain the dangerous ingredient squalene, which has been directly linked with cases of Gulf War Syndrome and a host of other debilitating diseases.
It was also recently reported that the UK government sent a confidential letter to senior neurologists telling them to be on the alert for cases of a brain disorder called Guillain-Barre Syndrome (GBS), which could be triggered by the vaccine.
Following the leak of the letter a senior neurologist told the Daily Mail, “I would not have the swine flu jab because of the GBS risk.”
The last attempt to mass vaccinate the public against swine flu, during the 1976 outbreak in the United States, killed more people than the virus itself.
The vast majority of respondents to the London Times article about the nurses’ refusal to take the shot commented that they too would refuse to take the vaccine, mirroring sentiment across the country.
At this stage only a deadlier return of the virus backed by a massive government fearmongering campaign is going to make anything like a majority of the population take the swine flu shot.
Since the majority of the population will refuse to take the vaccine, the government’s only option will be to institute a mandatory program backed by force, or to drop plans for mass vaccination altogether.
Vaccine More Dangerous Than Swine Flu.
By Dr. Russell Blaylock.
What the good doctor say is true. Don’t be taken for a ride. So what if you catch this mild 3-4 days flu. It is even weaker than seasonal flu. We need to counter all the MSM propaganda BS that we should look to vaccines to save us! Dr Blaylock writes:
An outbreak of swine flu occurred in Mexico this spring that eventually affected 4,910 Mexican citizens and resulted in 85 deaths. By the time it spread to the United States, the virus caused only mild cases of flu-like illness.
Thanks to air travel and the failure of public health officials to control travel from Mexico, the virus spread worldwide. Despite predictions of massive numbers of deaths and the arrival of doomsday, the virus has remained a relatively mild disease, something we know happens each year with flu epidemics.
Worldwide, there have only been 311 deaths out of 70,893 cases of swine flu. In the United States, 27,717 cases have resulted in 127 deaths. Every death is a tragedy, but such a low death rate should not be the basis of a draconian government policy.
It is helpful to recall that the Centers for Disease Control with the collusion of the media, constantly tell us that 36,000 people die from the flu each year, a figure that has been shown to be a lie. In this case, we are talking about 300 plus deaths for the entire world.
This virus continues to be an enigma for virologists. In the April 30, 2009 issue of Nature, a virologist was quoted as saying,“Where the hell it got all these genes from we don’t know.” Extensive analysis of the virus found that it contained the original 1918 H1N1 flu virus, the avian flu virus (bird flu), and two new H3N2 virus genes from Eurasia. Debate continues over the possibility that swine flu is a genetically engineered virus.
Naturally, vaccine manufacturers have been in a competitive battle to produce the first vaccine. The main contenders have been Baxter Pharmaceuticals and Novartis Pharmaceuticals, the latter of which recently acquired the scandal-ridden Chiron vaccine company. Both of these companies have had agreements with the World Health Organization to produce a pandemic vaccine.
The Baxter vaccine, called Celvapan, has had fast track approval. It uses a new vero cell technology, which utilizes cultured cells from the African green monkey. This same animal tissue transmits a number of vaccine-contaminating viruses, including the HIV virus.
The Baxter company has been associated with two deadly scandals. The first event occurred in 2006 when hemophiliac components were contaminated with HIV virus and injected in tens of thousands of people, including thousands of children. Baxter continued to release the HIV contaminated vaccine even after the contamination was known.
The second event occurred recently when it was discovered that Baxter had released a seasonal flu vaccine containing the bird flu virus, which would have produced a real world pandemic, to 18 countries. Fortunately, astute lab workers in the Czech Republic discovered the deadly combination and blew the whistle before a worldwide disaster was unleashed.
Despite these two deadly events, WHO maintains an agreement with Baxter Pharmaceuticals to produce the world’s pandemic vaccine. Novartis, the second contender, also has an agreement with WHO for a pandemic vaccine. Novartis appears to have won the contract, since their vaccine is near completion. What is terrifying is that these pandemic vaccines contain ingredients, called immune adjuvants that a number of studies have shown cause devastating autoimmune disorders, including rheumatoid arthritis, multiple sclerosis and lupus.
Animal studies using this adjuvant have found them to be deadly. A study using 14 guinea pigs found that when they were injected with the special adjuvant, only one animal survived. A repeat of the study found the same deadly outcome.
So, what is this deadly ingredient? It is called squalene, a type of oil. The Chiron company, maker of the deadly anthrax vaccine, makes an adjuvant called MF-59 which contains two main ingredients of concern—squalene and gp120. A number of studies have shown that squalene can trigger all of the above-mentioned autoimmune diseases when injected.
The MF-59 adjuvant has been used in several vaccines. These vaccines, including tetanus and diphtheria, are the same vaccines frequently associated with adverse reactions.
I reviewed a number of studies on this adjuvant and found something quite interesting. Several studies done on human test subjects found MF-59 to be a very safe immune adjuvant. But when I checked to see who did these studies, I found—to no surprise—that they were done by the Novartis Pharmaceutical Company and Chiron Pharmaceutical Company, which have merged. They were all published in “prestigious” medical journals. Also, to no surprise, a great number of studies done by independent laboratories and research institutions all found a strong link between MF-59 and autoimmune diseases.
Squalene in vaccines has been strongly linked to the Gulf War Syndrome. On August 1991, Anthony Principi, Secretary of Veterans Affairs admitted that soldiers vaccinated with the anthrax vaccine from 1990 to 1991 had an increased risk of 200 percent in developing the deadly disease amyotrophic lateral sclerosis (ALS), also called Lou Gehrig’s disease. The soldiers also suffered from a number of debilitating and life-shortening diseases, such as polyarteritis nodosa, multiple sclerosis (MS), lupus, transverse myelitis (a neurological disorder caused by inflammation of the spinal cord), endocarditis (inflammation of the heart’s inner lining), optic neuritis with blindness and glomerulonephritis (a type of kidney disease).
Because squalene, the main ingredient in MF-59, can induce hyperimmune responses and induce autoimmunity, a real danger exists for prolonged activation of the brain’s immune cells, the microglia. This type of prolonged activation has been strongly associated with such diseases as multiple sclerosis, Alzheimer’s disease, Parkinson’s disease, ALS and possibly vaccine-related encephalitis. It has been shown that activation of the systemic immune system, as occurs with vaccination, rapidly activates the brain’s microglia at the same time, and this brain inflammation can persist for long periods.
So, how would the gp120 get into the brain? Studies of other immune adjuvants using careful tracer techniques have shown that they routinely enter the brain following vaccination. What most people do not know, even the doctors who recommend the vaccines, is that most such studies by pharmaceutical companies observe the patients for only one to two weeks following vaccination—these types of reactions may take months or even years to manifest.
It is obvious that the vaccine manufacturers stand to make billions of dollars in profits from this WHO/government-promoted pandemic. Novartis, the maker of the new pandemic vaccine, recently announced that they would not give free vaccines to impoverished nations—everybody pays.
One must keep in mind that once the vaccine is injected, there is little you can do to protect yourself—at least by conventional medicine. It will mean a lifetime of crippling illness and early death.
There are much safer ways to protect oneself from this flu virus, such as higher doses of vitamin D3, selective immune enhancement using supplements, and a good diet.
What To Do If Force Vaccinated?
By Dr. Russell Blaylock.
Dr Blaylock has had first hand experiences with the A/H1N1 swine flu. He is a board certified neurosurgeon, author and lecturer. In the event that you or your loved ones are forced vaccinated, here is what Dr Russell Blaylock recommends:
Dr Blaylock recommends that following vaccination it will help to keep the immune reaction under control if:
i) All children get 5,000 units a day for two weeks after the vaccine and then 2,000 a units a day thereafter;
ii) Adults get 20,000 units a day after the vaccine for two weeks, then 10,000 units a day thereafter;
iii) And with that adults should take 500-1000 mg of calcium a day and children under the age of 12 years should take 250 mg a day, as vitamin D works more efficiently in the presence of calcium.
The Engineering of ‘Pandemics’.
By A. True Ott, PhD, ND
The year was 1921. America was entering a decade of robust prosperity. Later called “The Roaring Twenties”, it was a time of unparalleled economic expansion. Debt money from Wall Street banks was plentiful and easy to obtain. The “Great War” was over.
America was flexing her industrial muscles. Factories were being built and expanded in every major city. Automobiles began rolling off Detroit assembly lines in record numbers. The stock market began making millionaires. People were HEALTHY and HAPPY ¬ largely because the dreaded “world mystery disease” (which decades later became known as the “1918 Flu Pandemic”) had disappeared. Two entire years had passed with no dreaded “mystery deaths” being reported. America had cause to celebrate, and celebrate they did!
As a matter of fact, the American Public in general was so optimistic and HAPPY in 1921, that relatively few people were unhealthy as well. For the first time in decades, hospital beds were empty. The fledgling American Medical Association, formed by John D. Rockefeller just a few years earlier, was worried. Business was sagging.
Profits from vaccines and drugs were spiraling. Something had to be done, and done immediately. False, faux epidemics of smallpox were created to solve the problem, and keep the Medical Mafia’s cash registers ringing.
We know this dastardly plan actually happened, thanks to a citizen’s WATCHDOG GROUP in Kansas City, Missouri named “The Advertiser’s Protective Bureau”, who filed, and successfully prosecuted criminal charges against the Missouri state chapter of the AMA ¬ the Jackson Medical Society. The ‘Protective Bureau’s” official report of this cold-blooded plot reads as follows:
“In the Fall of 1921, the health of the city was unusually good, but slow for the doctors. So the Jackson Medical Society met and resolved to make an epidemic in the city. According to the minutes of this meeting: ‘MOTION WAS MADE AND SECONDED, THAT A RECOMMENDATION BE MADE BY THE COMMITTEE, TO THE BOARD OF HEALTH, THAT AN EPIDEMIC OF SMALLPOX BE DECLARED IN THE CITY. (Investigation later revealed that there was NO SIGN OF AN EPIDEMIC at the time, in the city, or anywhere in the state or region!)
‘It was moved and seconded that a day be set aside, termed VACCINATION DAY, on which physicians would be stationed at ALL SCHOOLS, clinics, public buildings and hospitals to vaccinate “free of charge”. (Vaccinations are never “free”. The taxpayers are always forced to pay for every one of the “free” vaccines.)
“IT IS FURTHER RECOMMENDED THAT WIDE PUBLICITY BE GIVEN, STATING THAT VACCINATION IS A PREVENTIVE OF SMALLPOX, AND URGING THE ABSOLUTE NECESSITY OF VACCINATION FOR EVERY MAN, WOMAN, AND CHILD IN THE CITY.”
The Protective Bureau proved in court that there WAS NO EPIDEMIC before the vaccinations!! The court records show that the Medical Society manufactured vast amounts of posters, fliers, newspaper stories and ads featuring horrific and lurid pictures of diseased children covered with massive smallpox sores and open wounds. Some pictures actually showed children’s corpses covered with the same ugly sores. The PANIC-DRIVEN message was clear — VACCINATE EVERYONE, or face a deadly public disease. There was a “sweeping epidemic” in the city; the disease was “highly contagious” and would “strike anyone who was not vaccinated” was the bill of goods sold! (Does this sound at all familiar today ¬ 88 years later??)
The Medical Mafia’s propaganda blitz was successful, and over a million previously healthy and happy American citizens were hypnotized and terrorized into placing the vaccine toxins into their bloodstreams. All public school children in the region were vaccinated while at school! Parents who dared question the vaccination of their children were ostracized and publicly vilified.
THE COURT RECORD ON THIS CASE IS VERY CLEAR. In the weeks and months following the “mass vaccinations” ¬ the area’s hospital beds were filled to over-flowing with VACCINE-INDUCED SMALLPOX CASES!
Tens of thousands of people became ill, and many hundreds of innocents died, and many more were permanently crippled! Of course, THE NEWSPAPERS THEN TRUMPETED HOW WISE THE MEDICAL ESTABLISHMENT WAS TO PROMOTE THE VACCINES - stating how much worse the death toll would have been without the vaccination campaign!! Untold MILLIONS OF DOLLARS of profit was generated by this massive “medical” fraud.
Thanks to the ADVERTISER’S PROTECTIVE BUREAU, however; the massive fraud was exposed and criminally prosecuted to a successful conviction. During the trial, three amazing facts were proven beyond any “reasonable doubt”.
Fact 1:
The poster and advertising pictures showing the diseased and dying children used so successfully by the “doctors”, WERE NOT EVEN CASES OF LOCAL SMALLPOX CASES AS THEY WERE BILLED TO BE! The Protective Bureau documented that they were pictures of ENGLISH CHILDREN who were victims of “court-proven” cases of SMALLPOX VACCINE POISONING!! One of the pictures was of a 5-week-old baby named Mona Stevenson, of Humphrey Street, Burnley, England. A previously healthy and happy baby, Little Mona had been vaccinated for smallpox at 5 weeks of age.
Four weeks later, her pox-ridden little body was placed in a tiny coffin and buried. The horrific photos of Little Mona and others in England had previously been published in British newspapers where details of the resulting CRIMINAL TRIALS were also given. The full details of the trials, as well as the pictures, were also included in a comprehensively large medical boot titled “THE HISTORY AND PATHOLOGY OF VACCINATION” by Edgar M Crookshank, MD ¬ professor of Bacteriology at the ultra-elite Kings College, London England.
Fact 2:
Vaccines containing LIVE VIRUSES, weakened (i.e. attenuated) or otherwise universally causes more diseases than the vaccine ever could prevent.
Fact 3:
Vaccine-Induced-Disease (VID) is an extremely effective socio-economic tool. It has the potential to generate BILLIONS OF DOLLARS OF WINDFALL PROFITS, while permanently changing the social structures of large groups of people.
While the Protective Bureau won the criminal court case - the American People lost. The case should have made front-page headlines around the nation, showing the Modus Operandi of certain corrupt “medical practitioners”. How, by means of fraud, treachery, and trickery, they made millions of dollars in windfall profits while thousands of innocent, trusting, and naïve Americans suffered and died. The entire sordid affair, with all its damning details, was kept out of the American Press. John D. Rockefeller’s AMA, with its millions of dollars of influence ¬ made sure of that!
Amazingly, even though thousands of people had died or become crippled by this managed manslaughter, the doctors involved were only given a light penalty in the form of a token fine. The medical establishment as a whole was not upset in the least by the exposure ¬ and has continued on unabated perpetuating the same crimes against humanity ¬ creating vaccine-induced-diseases while fleecing the people continually until this present day.
It is a proven (albeit little-known) fact, EPIDEMIC/PANDEMIC MANUFACTURING IS STANDARD PRACTICE with the world-wide “Medical Mafia” circles. In order to maximize profits and re-shape geographical regions, they often manufacture a false-flag “emergency”. If there is an outbreak of mild seasonal virus, they call it an influenza pandemic, give it a fancy new name, and then actually CREATE THE PANDEMIC by means of mass vaccinations using ATTENUATED, or LIVE VIRUSES!! Remember the shocking words of the AMA’s Dr. Simon Louis Katzoff who said: ” DOCTORS LIVE BY DISEASE, SO THE PUBLIC CAN EXPECT THE SUPPLY OF DISEASE TO MEET THE DEMANDS OF THE MEDICAL PROFESSION.”
OTHER DOCUMENTED CASES OF V.I.D.E.O.s (Vaccine Induced Disease Epidemic Outbreaks):
This vaccine-induced, manmade “epidemic” resulted in 330 deaths and at least 1,680 cases of severe smallpox that caused permanent, crippling damage to the survivors. Moreover, it cost the city a total monetary loss of $3,069,616; although Dr. Voux and his accomplices had collected more than $10 million in hospital and related care revenues ¬ they were not forced to pay for damages or reparations. As in the Kansas City trial, a small, insignificant fine was levied, and the case was not widely publicized.
As a result, polio increased a whopping 300% in these states. For example, Tennessee reported 119 polio cases in 1958, after “vaccination” this total increased to 386 cases in 1959, Ohio ¬ 17 cases in 1958, 52 cases in 1959, Connecticut ¬ 45 cases in 1958, 123 cases in 1959, and North Carolina: 78 cases in 1958 compared to 312 cases in 1959 AFTER forcing compulsory shots in school children. The modern record is equally damning. The ONLY cases of recorded polio in the modern era is immediately following vaccinations.
Poliomyelitis, you see, is a water-borne virus and is caused by drinking contaminated water. During the early 60’s, water-treatment facilities became standardized across America ¬ small amounts of CHLORINATION effectively wiped out polio viruses. The conquering of polio had NOTHING TO DO with the vaccine needles and swallowing sugar cubes.
In fact, as author Ed Haslem documents so well in his book, “http://doctormarysmonkey.com/” Dr. Mary’s Monkey, the Sabin vaccines were actually contaminated with mutated GREEN MONKEY VIRUSES (SV-40 viruses to be specific) which has caused untold millions of SOFT-TISSUE CANCERS and deaths worldwide. (The cancer “industry” has reaped BILLIONS of dollars from this “contamination” over the years, of course.) “http://www.youtube.com/watch?v=edikv0zbAlU” Dr. Maurice Hilleman has actually confessed as being a part of this very activity.
President Gerald Ford, (with proven ties to Big Pharma and Nixon’s covert viral weapons labs ¬ also a key member of the “Warren Commission’s” obfuscation of the JFK murder) rolls up his sleeves on national TV and dutifully takes the vaccine. 40 million vaccines are given to naïve American human guinea pigs. A rash of auto-immune disorders (Guillan-Barre Syndrome GBS, and lupus) as well as a large number of deaths is immediately attributed to the vaccine, and the mass vaccination campaign is halted. (What happened to the other 140 million vaccines, one may ask?)
In 1979, the television news magazine 60 Minutes did a documentary investigation on this travesty-for-money scandal. Against all odds and the threats of Big Pharma, the OBJECTIVELY FAIR 60 Minutes program aired ONE TIME. There was no follow-up story, No criminal indictments were ever issued. There was no MASS- MURDER-FOR-HIRE trial. As a result, America has largely forgotten the 1976 SWINE FLU SCANDAL! Click here for “http://www.youtube.com/watch?v=5lcJt4jX1Vo” Part I of the 60 Minutes story; and “http://www.youtube.com/watch?v=r4c9Is1T3z4″
Part II.
ALL MODERN “PANDEMICS” ARE CAUSED BY VACCINE NEEDLES.
As this author has repeatedly declared during many public radio interviews, the deadly 1918 Influenza Pandemic was the direct result of live-virus-contaminated Typhus Fever Vaccines mandatorily given to U.S. and Allied military personnel during World War I. During that era, viruses were not yet discovered and diseases were thought to be bacterial only. These deadly typhus fever vaccines were manufactured by John D. Rockefeller’s research labs and Chinese pharma factories. The vaccine “seed stock” consisted of viruses harvested from human typhoid fever patients, cross-injected into swine herds to create increased “seed stock”, and then injected into chicken and turkey eggs for further incubation of the pathogens. The final, harvested “vaccine material” then was injected into HUNDREDS OF MILLIONS OF HUMAN VEINS. The result was a massive ‘pandemic’ that claimed the lives of as many as 50 million people worldwide.
In 1918, the viral pandemic was an honest mistake - the result of a combination of a very bad vaccine and gross ignorance about viruses and the diseases they cause. However, the continued denial of these FACTS, and the subsequent REVERSE ENGINEERING OF THE KILLER VIRUS in Ft. Detrick labs (1997-2003) is inexcusable and constitutes a veritable crime against humanity.
Moreover, the ONLY WAY a modern “SWINE FLU PANDEMIC” can actually materialize is by injection of certain LIVE VIRUSES via vaccine needles. Make no mistake, the world is NOT experiencing a true pandemic explosion at this time ¬ but it most assuredly WILL when and if the planned mass influenza vaccinations are completed worldwide.
THE DANGERS INHERENT IN “DUPLEX” VACCINES FROM DESIGNER VIRUSES.
“Modern Medical Practitioners”, including some well-meaning “osteopaths”, would have the world believe the MYTH that vaccines containing attenuated (weakened) live viruses cannot cause the viral disease conditions they are targeting. This is a most dangerous misconception for the following SCIENTIFIC reasons.
Traditional “common” vaccines targeting measles, mumps and rubella for instance, contain small amounts of “attenuated” live viruses which have been “weakened” but not 100% killed outright. Research has shown that these weakened “live” viruses create a very mild form of the disease in the human that has been vaccinated, which in turn creates a cellular immunity from that pathogen. The science behind this is correct, and valid for the most part. To keep the targeted viral pathogen in a perpetually weakened state, specific amounts of formaldehyde and ether are typically added, and in some formulations, mercury in the form of thimerasol is added as a preservative to keep the egg albumin cells from decaying and dying prematurely.
The established theory behind all of this ‘vaccination’ is the “protect the herd” theory which originated with Pasteur in the late 19th century. As in all vaccines, a certain small percentage of the herd will develop severe, ‘full blown’ disease states CAUSED by the attenuated viruses in the vaccine itself, and another percentage will exhibit side effects from the chemicals added to the vaccine ¬ but if the vast majority of the herd is “protected” from the disease condition - the vaccine is approved and stamped “safe and effective”.
Science has also proven that each viral pathogen has its own unique characteristics that produce its own set of symptoms in the human hosts. Thus, each viral pathogen has its own unique fingerprints of replication and reproduction as well. Each virus also has a different level of effectiveness in its attenuated (weakened) state.
Moreover, some viruses have shown the ability to “drift” and acquire additional genetic alterations over time. THIS IS ESPECIALLY TRUE OF THE SO-CALLED “NOVEL” RECOMBINATION VIRUSES that have been “reverse engineered” in the world’s weapons laboratories!
When the RNA of the virus is spliced with other viral genes, the resulting “Franken-virus” is very unpredictable. Studies conducted (yet currently unpublished) by Terrence Tumpey, Jeffrey Taubenberger, and others at the NIH and CDC show that these ‘resurrected pandemic viruses’ do not exhibit the NORMAL tendencies of traditional, NATURAL influenza viruses such as seasonal H3N2 human strains. They are best described as “Viral Wild Cards”.
This is just one problem with the headlong, mad rush to vaccinate Americans with a series of reverse-engineered lab-created viruses, attenuated or otherwise, in an UNTESTED, UNTRIED, EXPERIMENTAL VACCINE that has not been subjected to LONG-TERM CLINICAL TRIALS TO DETERMINE THE LEVELS OF “DRIFT” or even ATTENUATED TENDENCIES OVER TIME.
To supposedly minimize this “safety” issue, the CDC is now recommending a DUPLEX vaccination, of all things. A “duplex” vaccination basically involves a two-shot series. The first shot consists of a VERY WEAK, HIGHLY ATTENUTATED dose of the live virus. This is intended to create an initial immune response patterning the specific virus injected. Within a couple of weeks of the 1st shot, a BOOSTER SHOT is given. The booster shot has only lightly attenuated, or even FULL STRENGTH VIRUSES in the injection. This 2nd shot is then intended to create a full-strength immune system response in the human subject.
This is, at the very least, BAD SCIENCE and borders on insanity for self-evident and fairly obvious reasons. By their own admissions, the NIH scientists in their various writings have declared that the level of potency of these REVERSE ENGINEERED VIRUSES show abnormal, almost RANDOM tendencies in their attenuated states. Nobody really knows what will happen over time as the inevitable “genetic drifts” occur. It is a literal crap shoot. It is highly probable that even the HIGHLY ATTENUATED FRANKEN-VIRUSES can swiftly regain their FULL POTENCY even in the presence of ether and formaldehyde. (See Addendum Below) Secondly, the full-strength BOOSTER shot viruses could just as easily “DRIFT” into something much more deadly than the “original’ recombinant virus that it is targeting.
I submit that the scientists responsible for this “pandemic” are not stupid. They have to know these facts as well as I do.
Therefore, I can only conclude that this entire affair is following the Modus Operandi of the medical elite since the 1920 engineered smallpox epidemics. It is all being ORCHESTRATED first and foremost for MONEY, and secondly, for social and geographical restructuring of the “human herd”.
Also, it must be understood that this “Novel 2009 Influenza” is not easily nor readily transmissible between humans. (See published study in the addendum). If this report is accurate, how then did the “Pandemic” begin, and why the need for mass vaccinations at all?? Like the “study” shows, the only way the test ferrets could contract or transmit the 2009 “Novel Swine Flu” was by and through INOCULATION OF THE DISEASE!! Humanity demands an answer, and demands it NOW!
Der Beipackzettel zum Impfserum.
Der Beipackzettel für den H1N1 2009 Monovalent Impfstoff der von Novartis hergestellt wird ist im Internet veröffentlicht worden. Darin steht, der Impfstoff basiert auf einen Vorgänger genannt Fluvirin und kann eine ganze Reihe von erheblichen Nebenwirkungen und Gesundheitsschäden bewirken, wie das Guillain-Barre Syndrome, Vaskulitis, anaphylaktischer Schock und sogar den Tod.
Jeder der sich mit den Nebenwirkungen des Impfstoff beschäftigt hat weiss was dieser alles auslösen kann, aber das Besondere hier ist, nun führt der Beipackzettel der Schweinegrippeimpfung alle diese Schäden auch auf und Novartis gibt es damit zu. Auf dem Zettel steht als Datum September 2009, also ist es der neueste Stand der Information.
Im Beipackzettel steht, dass für Kinder zwischen 4 und 8 Jahren zwei Injektionen a 0,5 ml mit einem Abstand von einem Monat gespritzt werden. Kinder ab 10 Jahren und Erwachsene bekommen nur eine Spritze a 0,5 ml.
Im Beipackzettel steht auch, die Dosis von 0,5 ml beinhaltet Thiomersal als Konservierungsmittel bestehend aus Quecksilber in einer Menge von 25 Mikrogramm. Quecksilber ist ein Nervengift und sollte deshalb vermieden werden. Wegen der kumulierenden Quecksilberbelastung von Kindern durch die routinemässigen Kinderimpfungen wird vermutet, neurologische Störungen wie z. B. Autismus wird dadurch ausgelöst.
Wenn man sich die weiteren aufgeführten Nebenwirkungen ansieht, dann wird es einem ganz anders, wie zum Beispiel: Schmerzen an der Impfstelle, Ausschläge, Schwellungen, Schüttelfrost, Fieber, Müdigkeit, Asthenie, Gesichtsödeme, Störung des Immunsystem, Überempfindlichkeitsreaktionen die zu Schockzuständen und Tod führen können, Herz-Kreislaufstörungen, Vaskulitis, Ohnmachtsanfälle, Verdauungsstörungen, Durchfall, Übelkeit, Erbrechen, Bauchschmerzen, Blut- und Lymphstörungen bis hin zu Paralyse und Gehirnschäden.
Da erscheint es fast vernünftiger die Grippe einfach durchzustehen und mit den üblichen Hausmitteln auszukurieren als sich diesen Giftcocktail reinspritzen zu lassen.
Schweinegrippe wegen Impfung?
Marburg/München - Wer sich gegen die saisonale Grippe impfen lässt, hat möglicherweise ein erhöhtes Risiko, an der Schweinegrippe zu erkranken. Laut einer vom Nachrichtenmagazin „Focus“ zitierten, bislang unveröffentlichten Untersuchung kanadischer Forscher verdoppelt die Grippeimpfung das Risiko einer Schweinegrippe-Infektion. Nach kanadischen Zeitungsberichten wollten die meisten Provinzen deshalb den normalen Grippeschutz vorerst nur über 65-Jährigen zugänglich machen, berichtet das Nachrichtenmagazin.
„Die Studie ist noch nicht veröffentlicht, es gibt bislang nur Gerüchte“, sagte der Direktor des Instituts für Virologie an der Marburger Philipps-Universität, Professor Dr. Stephan Becker. Sollten sich die Angaben bewahrheiten, hätte dies möglicherweise Auswirkungen auf die Grippe-Impfungen in Deutschland: Laut Becker ist es denkbar, dass generell zunächst gegen die pandemische und dann gegen die saisonale Grippe geimpft wird.
dpa, Montag, 05. Oktober 2009, 10:15 Uhr
Kanzlerin und Minister sollen speziellen Impfstoff erhalten.
Vor einigen Tagen hatte die Bundeswehr bekanntgegeben, dass sie für ihre Soldaten einen Impfstoff ohne Zusatzstoffe geordert hat.
Doch nach SPIEGEL-Informationen sollen auch weitere Personengruppen eine Impfung ohne Adjuvantien erhalten: "Wir haben 200.000 Dosen des nicht-adjuvantierten Impfstoffs Celvapan der Firma Baxter gekauft", räumt Christoph Hübner, Sprecher des Bundesinnenministeriums ein. Anders als das Präparat von GlaxoSmithKline (GSK), das ab kommender Woche in 50 Millionen Dosen für die Bevölkerung ausgegeben wird, enthält der Baxter-Impfstoff keinen Wirkverstärker.
Allerdings kommt Celvapan nur deshalb ohne die umstrittenen Hilfsstoffe aus, weil es eine größere Konzentration an inaktivierten Schweinegrippeviren enthält als die beiden anderen Impfstoffe. Die Substanz wird den für die Aufrechterhaltung der öffentlichen Ordnung zuständigen Staatsdienern gespritzt: Mitgliedern des Kabinetts sowie Beamten der Ministerien und der nachgeordneten Behörden. Dazu zählen auch die Mitarbeiter des für die Impfstoffzulassung zuständigen Paul-Ehrlich-Instituts, das vergangene Woche wiederholt seine Entscheidung verteidigt hat, der Bevölkerung die GSK-Vakzine zu beschaffen.
"Gesundheitsbehörden sind auf Pharmakonzerne hereingefallen"
Für den Vorsitzenden der Arzneimittelkommission der deutschen Ärzteschaft, Wolf-Dieter Ludwig, ist das ein Skandal, der den Menschen kaum zu vermitteln sei. "Wir sind unglücklich über diese Impfkampagne", so Ludwig weiter. Sie werfe zahlreiche Probleme auf, ihr Nutzen sei ungewiss: "Die Gesundheitsbehörden sind auf eine Kampagne der Pharmakonzerne hereingefallen, die mit einer vermeintlichen Bedrohung schlichtweg Geld verdienen wollten."
Weil der GSK-Impfstoff nicht an Schwangeren getestet wurde, muss auch für sie kurzfristig nicht-adjuvantierter Impfstoff besorgt werden. Das zuständige Thüringer Gesundheitsministerium hatte am Freitag erklärt, man verhandle mit verschiedenen Herstellern über einen begrenzten Nachkauf von Impfstoff ohne die umstrittenen Hilfsstoffe. Der Staatssekretär im Bundesgesundheitsministerium, Klaus Theo Schröder, bestätigte das gegenüber dem SPIEGEL: "Es laufen derzeit Gespräche mit Herstellern sowie den Gesundheitsministerien in Frankreich und den USA, mit dem Ziel, für Schwangere auch nicht-adjuvantierten Impfstoff zu beschaffen."
Offene Rebellion herrscht unter Allgemeinmedizinern und Kinderärzten. Der Präsident der Deutschen Gesellschaft für Allgemeinmedizin und Familienmedizin, Michael Kochen, rät den deutschen Hausärzten von der Impfung ab. "Das Schadensrisiko überwiegt den Nutzen", sagt der Göttinger Professor. Wolfram Hartmann, Präsident des Berufsverbands der Kinder- und Jugendärzte, wirft der Bundesregierung "wissenschaftliche Falschaussagen" vor. Wie bei Schwangeren, so gelte auch für Kinder unter drei Jahren: "Der Impfstoff ist an ihnen noch überhaupt nicht getestet, deshalb ist das Risiko einfach zu groß, ihn jetzt bedenkenlos einzusetzen."
Kinder hätten ein Immunsystem, das zu Überreaktionen neige, genau die aber könnten durch den Zusatz von Wirkverstärkern ausgelöst werden. Zusätzlich sei dem Impfstoff auch noch ein quecksilberhaltiger Konservierungsstoff beigefügt. "Das Zeug hat man in heutigen Impfstoffen für Kleinkinder bewusst herausgehalten", sagte Hartmann.
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