And 1984 becomes more real everyday
Tagged: safety Toggle Comment Threads | Keyboard Shortcuts
Adventures in Autism
September 15, 2009
A participant in the german H1N1 vaccine trials reports serious adverse reactions, including coughing up blood, but the lead researcher blows it off. Yet another story of problems in vaccine safety studies that are ignored.
Why test a vaccine exactly, if you already have decided what the outcomes can or cannot be? Apparently Heir Doctor will only accept ‘redness and swelling at the injection site’ as a side effect.
The article does not say which version of the vaccine he got. Wish there was more information on this case.
Swine flu vaccination: A test subject speaks out.
Translation into English by Erwin Alber
Munich – A harmless prick – and thereby possibly save thousands of people. This is what several hundreds of volunteers thought, who each collected a payment of 250 Euro for their participation in the study of the swine flu vaccine trial at the Ludwig-Maximilians-University.
One of them has now quit the trial: The Diploma-businessman Axel Sch. (40). He claims : “The vaccination has made me ill! – the test is irresponsible.” He says that within a few hours after the vaccination, on August 10, he had sweat on his forehead. “I felt totally beat. On the third day, my kidneys and head were aching and I got a fever. I then had a coughing fit – and the wash basin was suddenly red – it was blood!“
LMU-medical researcher Frank von Sonnenburg, who is in charge of the country-wide study, doesn’t consider these accounts credible. He says that such side-effects cannot be related to the vaccine. He does not deny that, as with other flu-vaccinations, flu-like symptoms may occur as a reaction to the vaccination. “Additionally, there may be light pain, redness or swelling at the injection site.”
“Obviously many of the test subjects would have side-effects. We do such a study precisely because we want to find out any possible side-effects. If flu cases were to become more severe and we had not done any tests, – there would be a big outcry by everyone.”
Was the vaccine admitted too quickly to the study? The fact is that in this composition, the vaccine has not yet been applied to humans. The Federal Health Minister Ulla Schmidt explained on Wednesday that she had felt put under pressure by the pharmaceutical industry from the beginning. Criticism is being voiced with increasing frequency. The Paul-Ehrlich-Institute points out that side-effects to this vaccine are to be more expected than in connection with a normal flu-vaccine. The Paediatric Association points to a possibly increased number of unknown side-effects.
British researchers even warn about a neurological disorder known as the Guillain-Barré-Syndrome. They point to a vaccination campaign with a similar swine flu vaccine carried out in the USA in 1976, which resulted in the deaths of 25 people.
Probably because of this, the USA only test vaccines without so-called adjuvants. These lead to greater side-effects, explains study leader Frank von Sonnenburg. “The adjuvants produce more anti-bodies, which is why the body’s defensive reaction is also greater.” Kidney pains and bloody cough of the kind Axel Sch. Experienced were however not to be expected, even with this adjuvant. “We conduct a clean study.”
Axel Sch. however insists that his complaints were a result of the vaccination. “Surely it is no coincidence that they occurred directly after the vaccination.” He criticizes the university, saying that he was not properly informed prior to the study. He said that for three days he was flat on his back during this heat. “When I phoned the LMU, they simply asked me the question needed to fill in their form and told me to see my doctor.” He now wants the medical costs and loss of earnings compensated by the medical insurance covering the trial.
Axel Sch. has participated in medical trials even when he was a student. He had also had good experiences with an LMU flu-vaccine study. “This is the reason why I immediately consented when they asked me if I would test the new vaccine.”
Now his trust in research is gone, he is quitting the vaccine trial. In October he will fly to Latin America for professional reasons. He had looked forward to traveling unconcerned – by then he would have received the second of three vaccinations. “I’m not fearful just the same – I don’t belong to an at risk group. Also, the swine flu can’t possibly be as bad as the side-effects of the vaccine.”
Spermicide, Cleaners, and Cosmetics along with Thimerosal and Squalene Found in Experimental H1N1 Vaccine
Jeffry John Aufderheide
September 14, 2009
See for yourself the study presented at the end of article. Please spread the word and make this go viral… no pun intended. Kindly reference and link to VacTRUTH!
Trials for the experimental H1N1 Swine flu vaccine commence Tuesday, September 15th in Thornton, Colorado. Novartis, a bio-pharmaceutical company that manufactures the vaccine, is recommending that children participating in the trial receive two doses of an experimental vaccine which contain ingredients found in spermicides, cleaners, and cosmetics along with thimerosal and squalene (MF59). Everyone should have a sense of concern as the only safety checks for these children are a few blood draws and follow-up phone calls. No neurological testing. No kidding.
Official opinions from federal agencies, such as the CDC, insist that the new vaccine will be safe and effective. Experts say we can trust the new H1N1 experimental vaccine because the technology used to create the vaccine is time tested. Experts argue that the only variable changing from the ‘normal’ flu vaccine and the H1N1 experimental vaccine is the novel A/H1N1 antigen. In other words, the same vaccine ‘technology’ is used but with the new virus.
However, this is the furthest thing from the actual TRUTH. As will be demonstrated, the following information was obtained through enrolling a family member into the study to gain an understanding as to what the ingredients would be. After finding out the the information I am about to share, enrollment in this trial has been canceled.
SETTING THE STAGE ON SAFETY AND SQUALENE (MF59)
I met with the research coordinator for the study along with Dr. Melamed, an immunologist conducting the study. Dr. Melamed altruistically shared his knowledge answering questions concerning immunology and the technology behind the vaccine while remaining evasive on questions of what was in the vaccine and legal ramifications if harm was done. Dr. Melamed reassured me several times that the experimental H1N1 vaccine was created just like past vaccines and that the technology was well established.
Requests for package inserts for the ingredients of the experimental H1N1 vaccine were denied on the grounds that this was a study and that information is privileged. However, we can still piece together some of the ingredients based upon the parental consent form.
“MF59 is an adjuvant which is used in influenza vaccines licensed for the adults and/or elderly in many countries worldwide, but it is not contained in any vaccines currently approved in the United States.” (page 2)
Isn’t it interesting that the study states it is licensed for adults and elderly? This study is designed for children between the ages of 3 and 8 and they plan on shooting up newborns and pregnant women with this stuff? Buyer beware.
Here is what the World Association for Vaccine Education had to say about Squalene (MF59):
Squalene:C30H50 an Adjuvant
Too dangerous for human use, Squalene is not licensed for use in the United States. Oil adjuvants like squalene have been ordinarily used to inflict diseases in animals – for experimentation and study. According to anthrax vaccine expert Gary Matsumoto and other reliable sources, the US military used an unlicensed, experimental anthrax vaccination laced with squalene, with disastrous consequences, including Gulf War Sydrome. Chemical descriptions:
Unites States National Library of Medicine: PubChem
Matsumoto, Gary. Vaccine A; The Covert Government Experiment That's Killing Our Soldiers – and Why GI's Are Only the First Victims. Basic Books, 2004.
Present in these vaccines:
Anthrax (experimental, used on military personnel)
Dr. Sherri Tenpenny also elaborates on the deleterious effects of the Squalene Adjuvant in a 2006 article entitled, "FLU SHOTS AND THE NEW ADJUVANTS: BEWARE!" and can be found in its entirety here. An excerpt from Dr. Tenpenny's article can give a better appreciation and understanding of what squalene is capable of in the body...
"On first blush, squalene seems like a good choice for an adjuvant. Manufactured naturally in the liver, squalene is a precursor for cholesterol. In addition, squalene can be purchased at health food stores in its more commonly known form, “shark liver oil.” However, ingested squalene has a completely different effect on the body than injected squalene. When molecules of squalene enter the body through an injection, even at concentrations as small as 10 to 20 parts per billion, it can lead to self-destructive immune responses, such as autoimmune arthritis and lupus.
Several mechanisms have been proposed to explain this reaction. Metabolically, squalene stimulates an immune response excessively and nonspecifically. More than two dozen peer-reviewed scientific papers from ten different laboratories throughout the U.S., Europe, Asia, and Australia have been published documenting the development of autoimmune disease in animals subjected to squalene-based adjuvants. A convincing proposal for why this occurs includes the concept of “molecular mimicry” in which an antibody created against the squalene in MF59 can cross react with the body’s squalene on the surface of human cells. The destruction of the body’s own squalene can lead to debilitating autoimmune and central nervous system diseases."
“Carcinogenicity, we (Dr. Deborah Novicki of Novartis, another pharmaceutical company) have done no testing for the carcinogenicity of MF59 adjuvant or any of our preventive vaccines. We haven’t done it and we don’t plan to.”
This information is found on a workshop on adjuvants and adjuvanted preventative and therapeutic vaccines hosted by the FDA. This gem of a quote is on page 391.
STRANGE BEDFELLOWS: THIMEROSAL AND SPERMICIDES
Further down we see that, while not mentioned explicitly as ingredients, one can deduce they are in the vaccine via an implied allergic reaction.
"If your child has had an allergic reaction in the past to eggs, egg products, neomycin or polymyxin (antibiotics), sodium ethylmercurothiosalicylate or thimerosal (compounds containing mercury that are frequently used as preservatives in vaccines), beta propriolactone (substance that inactivates a virus), or nonoxynol 9 (substance commonly used in cleaners, cosmetics, and spermicides), you must tell the medical staff..." (pg (emphasis mine)
Thimerosal has been thoroughly exposed as a neurological toxin largely in part and much gratitude to Lyn Redwood who obtained the meeting minutes from a secret meeting between government officials and pharmaceutical companies discussing the effects of the mercury additive. The document is called the Simpsonwood document and details exclusively the neurological harm thimerosal causes in children. Dr. Russell Blaylock has a commentary on the document here or read the meeting minutes yourself here.
“the number of dose related relationships [between mercury and autism] are linear and statistically significant. You can play with this all you want. They are linear. They are statistically significant.” – Dr. William Weil, American Academy of Pediatrics. Simpsonwood, GA, June 7, 2000
“the issue is that it is impossible, unethical to leave kids unimmunized, so you will never, ever resolve that issue [regarding the impact of mercury].” – Dr. Robert Chen, Chief of Vaccine Safety and Development, Centers For Disease Control, Simpsonwood, GA, June 7, 2000
“Forgive this personal comment, but I got called out at eight o’clock for an emergency call and my daughter-in-law delivered a son by c-section. Our first male in the line of the next generation and I do not want that grandson to get a Thimerosal containing vaccine until we know better what is going on. It will probably take a long time. In the meantime, and I know there are probably implications for this internationally, but in the meanwhile I think I want that grandson to only be given Thimerosal-free vaccines.” – Dr. Robert Johnson, Immunologist, University of Colorado, Simpsonwood, GA, June 7, 2000
“But there is now the point at which the research results have to be handled, and even if this committee decides that there is no association and that information gets out, the work has been done and through the freedom of information that will be taken by others and will be used in other ways beyond the control of this group. And I am very concerned about that as I suspect that it is already too late to do anything regardless of any professional body and what they say…My mandate as I sit here in this group is to make sure at the end of the day that 100,000,000 are immunized with DTP, Hepatitis B and if possible Hib, this year, next year and for many years to come, and that will have to be with thimerosal containing vaccines unless a miracle occurs and an alternative is found quickly and is tried and found to be safe.” – Dr. John Clements, World Health Organization, Simpsonwood, GA, June 7, 2000
One can only wonder the harmful effects nonoxynol 9 could bring.I could find no past flu vaccine that contained this ingredient nor study showing it is safe to inject into humans.
At this point, it must be said. According to the CDC’s vaccine schedule, children now receive 36 vaccines prior to going into kindergarten. This fall season will add 4 additional vaccines to this total for a grand total of 40!? And we’re not even getting warmed up…
POSSIBLE RISKS AND SIDE EFFECTS
By far the most entertaining part of the meeting with Dr. Melamed is when my eyes bugged out on page 6 and 7 of the study. It was explained to me that the side effects I am about to list off are side effects for all vaccines… and that I had nothing to worry about because this vaccine, this vaccine as you recall was made with ‘established technology’. If that is the case, it is the cause for even MORE concern!!!!
“Other side effects that have been reported in clinical studies with other influenza vaccines or have been reported by people who received influenza vaccines may include: [VacTRUTH Editor's Note: Potential Flu Symptoms Highlighted in RED]
Reactions at the site of injection:
• lump or irritation at the site where the vaccine was given
• sharp pain in or along nerves or tingling of pins and needles (paresthesia)
• pain limiting movement of the limb where the vaccine was given
• muscle ache
Other general reactions:
• hot flashes or flushing
• chills or shivering
• generalized weakness
• fainting shortly after vaccination
• loss of appetite
• abdominal pain
• back pain
• lymph node enlargement
• temporary decrease in the number of blood platelets, which may increase the risk of bleeding
• decrease in red blood cells, or anemia, which may make you feel tired.
• high blood pressure (hypertension)
• shortness of breath
• chest tightness
• chest pain
• sore throat
• runny nose
• “pins and needles” in the skin
• skin disorders related to allergic reaction (which can lead to rash and skin loss)
• inflammation of blood vessels (including inflammation of blood vessels that may cause short-term effect on kidneys)
• headaches similar to those described as migraine
• seizures associated with fever
• spinal cord or brain inflammation (encephalomyelitis)
• muscle weakness
• life-threatening and/or debilitating disorders of the nervous system“
On IMMUNoE’s website, on page three of this flier, it states:
“Q: Could the new H1N1 vaccine cause a person to get the flu?
A: Contrary to popular belief, it is not possible to get flu from a flu vaccine. This is true for the seasonal flu vaccine, as well as the investigational(sic) H1N1 vaccine.”
Are the vaccines the same or not the same? Of course, Dr. Melamed at this point tells me about how people with weakened or no immune system can actually get the disease from a vaccine. I asked what measures were being used to understand what the child’s immune response would be (or even if they had an immune response to indicate it was working PRIOR to the vaccine) and Dr. Melamed said, ‘none’. If they don’t measure before and after, how will they know?
“These other general conditions have occurred in people who received influenza vaccines:
• autoimmune disorders (these are disorders in which the body’s tissue are attacked by its own immune system and include liver injury or nerve injury)
• arthritis (joint pain)” (pg
DR ANDREW MOULDEN AND NEUROLOGICAL TESTING
Being a concerned parent one at this point would probably want to know how neurological damage is measured to know if it has occurred in their child. To my surprise, NO NEUROLOGICAL MEASUREMENTS are taken!!! Neurological damage can clearly be seen in past flu vaccines as was the case in the 1975-76 swine flu vaccine.
Dr. Andrew Moulden gives laypersons clinical skills to detect neurological damage occurring after a child or adult is vaccinated. I highly recommend his DVD – Tolerance Lost that is found on his Brainguard website or reading several articles posted exclusively on VacTRUTH which will give you these skills. They are respectively entitled, “Dr. Andrew Moulden (Interview): What You Were Never Told About Vaccines” and “Vaccinations are causing impaired blood flow (Ischemia), Chronic Illness, Disease and Death for us all“. The second article has photographs showing you precisely what is occurring.
In a separate interview with Dr. Moulden, he succinctly states that if neurological measures are never taken, the industry can say that vaccines are safe.
The only measurements taken will be a brief physical exam, measurement of vital signs and body temperature, blood samples to check for immune response, reviewing diaries with staff, and follow up phone calls. (pg4) Monitoring for safety is occurring for 13 months. How can, then, the vaccines be declared for public use with any certainty of safety in less than 2 months?
“It is also of the understanding that eight investigational (sic) vaccine formulations with different amounts of A/H1N1 antigens and with or without adjuvant will be tested for this study.” (pg 2)
Let us recap.
1. The vaccine contains squalene (MF59) which has not been tested for causing cancer.
2. The vaccine contains thimerosal, a known culprit in causing autism and neurological deficits.
3. The vaccine curiously contains nonoxynol-9 used in spermicides.
4. The vaccine will likely cause (and spread) the flu.
5. No neurological testing will be done to ensure the vaccine is safe from harmful neurological side effects.
6. Monitoring for safety will last 13 months, well beyond the flu season.
As to my knowledge, this information is the first of its kind validating the ingredients and the intent to use them on the population. Buyer beware of this vaccine as we are likely to see an onslaught of damaged men, women, and children if there are forced vaccines. The ‘new’ experimental vaccine is certainly unlike any other that we, as Americans, have been exposed to in the past.
VacTRUTH Editor’s Note:
1. Check out Jonathan Elinoff’s new website http://vaccinationeducation.com.
2. Dr. Sherri Tenpenny has a great site to educate yourself on the upcoming flu season at http://pandemicfluonline.com.
3. Dr. Mayer Eisenstein has a free webinar series talking about various topics in vaccinology. Visit his website at http://homefirst.com.
4. Read how pharmaceutical companies plan on superseding parental consent laws to force mass vaccinations here.
5. Visit InTheory.tv for interviews I have done concerning vaccines with Chris Yankowski.
Just Get There
July 30, 2009
The media is reporting on the governments preparation for a massive vaccination campaign this fall for the hyped up H1N1 hybrid flu virus. Recently Katherine Sebelius, the Health and Human Services Secretary, granted legal immunity for vaccine manufacturers during the stage 6 pandemic declared by the WHO. Even more troubling than the new vaccines or antivirals themselves, is the Emergency Use Authorization (EUA) declared by the FDA, which enables the use of expired stockpiles of Tamiflu or Relenza, and non-compliance with label requirements. The EUA authority will also permit the FDA to allow the use of “unapproved or uncleared medical products” during an established emergency.
A large percentage of the public who are informed of these facts will simply refuse the shot, but face government threats of home interventions through provisions in the Health Care bill, compulsory vaccination and quarantine.
The new stock of vaccines the governments purchased, has been fast tracked for approval by the FDA. Health officials admit that the clinical tests are about dosage amounts, and not safety. So the new vaccines being approved for the fall campaign, have the potential to cause severe harm or death, due to the lack of safety tests.
The AP reported
The clinical trials are mainly aimed at calibrating the doses to give to patients, not to test if it is safe or not, officials stressed.
“We are not trying to find some yet unrecognized problem with the vaccine,” said Michael Osterholm, director of the Center for Infectious Disease Research and Policy at the University of Minnesota
This is an appalling statement considering the 1976 mass vaccination campaign for swine flu, that injured hundreds of thousands and resulted in dozens of deaths from Guillain-Barré Syndrome. It is also a very cryptic statement, unrecognized problems, meaning that they will not explore how the body will react to new vaccines with unapproved adjuvants like Squalene.
Meryl Nass, M.D., an authority on the anthrax vaccine, stated on her blog:
“A novel feature of the two H1N1 vaccines being developed by companies Novartis and GlaxoSmithKline is the addition of squalene-containing adjuvants to boost immunogenicity and dramatically reduce the amount of viral antigen needed. This translates to much faster production of desired vaccine quantities.”
Dr. Mercola explains the effects of squalene injected into humans in this excerpt from his article on the subject:
The difference between “good” and “bad” squalene is the route by which it enters your body. Injection is an abnormal route of entry which incites your immune system to attack all the squalene in your body, not just the vaccine adjuvant.
Your immune system will attempt to destroy the molecule wherever it finds it, including in places where it occurs naturally, and where it is vital to the health of your nervous system.[viii]
Gulf War veterans with Gulf War Syndrome (GWS) received anthrax vaccines which contained squalene.[ix] MF59 (the Novartis squalene adjuvant) was an unapproved ingredient in experimental anthrax vaccines and has since been linked to the devastating autoimmune diseases suffered by countless Gulf War vets.[x]
The Department of Defense made every attempt to deny that squalene was indeed an added contaminant in the anthrax vaccine administered to Persian Gulf war military personnel – deployed and non-deployed – as well as participants in the more recent Anthrax Vaccine Immunization Program (AVIP).
However, the FDA discovered the presence of squalene in certain lots of AVIP product. A test was developed to detect anti-squalene antibodies in GWS patients, and a clear link was established between the contaminated product and all the GWS sufferers who had been injected with the vaccine containing squalene.
The WHO even admitted the swine flu vaccine being fast tracked in the EU may be unsafe because it allows firms to bypass large-scale human trials.
So with reduced safety testing, would you trust a vaccine manufacturer whose contaminated vaccine could have potentially caused a pandemic?
Baxter pharmaceutical, one of the drug firms contracted to produce the H1N1 vaccine, recently sent vaccines that contained the live avian flu virus to 18 countries.
A virologist stated that this could have caused a pandemic if it would have been injected into a human subject.
As published on LifeGen.de
“Baxter International Inc. in Austria ‘unintentionally contaminated samples with the bird flu virus that were used in laboratories in 3 neighbouring countries, raising concern about the potential spread of the deadly disease’. Austria, Germany, Slowenia and the Czech Republic – these are the countries in which labs were hit with dangerous viruses. Not by bioterrorist commandos, but by Baxter. In other words: One of the major global pharmaceutical players seems to have lost control over a virus which is considered by many virologists to be one of the components leading some day to a new pandemic.”
Dr. Mae-Wan Ho and Prof. Joe Cummins from The Institute of Science in Society stated “the vaccines are far more deadly than the swine flu; mass vaccinations are a recipe for disaster”
With this knowledge, there is no excuse for the government to give vaccine manufacturers legal immunity for injuries or deaths caused by these untested cocktails, for a flu that has killed less than 300 hundred people, with most having preexisting health issues.
Given the fact that the FDA has enabled the use of dangerous treatments for the diagnosis of swine flu via the declaration of the EUA, we shouldn’t be surprised for the lack of safety for new vaccines. It also makes sense that they would seek to protect themselves and vaccine manufacturers because they have the foreknowledge that these treatments are deadly.
A large percentage of the public who are informed of these facts will simply refuse the shot, but face government threats of home interventions through provisions in the Health Care bill, compulsory vaccination and quarantine.
Overruling individual human rights has been rationalized by the WHO in a 2005 pandemic preparedness document. The WHO Checklist for Influenza Pandemic has been adopted by several governments as a blueprint for the suspension of individual rights. Below is an excerpt from the WHO’s document that promotes overruling legislation and human rights .
1.5 Legal and ethical issues
1.5.1 Legal issues
During a pandemic, it may be necessary to overrule existing legislation or (individual) human rights. Examples are the enforcement of quarantine (overruling individual freedom of movement), use of privately owned buildings for hospitals, off-license use of drugs, compulsory vaccination or implementation of emergency shifts in essential services. These decisions need a legal framework to ensure transparent assessment and justification of the measures that are being considered, and to ensure coherence with international legislation (International Health Regulations).
Questions to be addressed
Is there a legislative framework in place for the national response plan? Does this framework include contingencies for health-care delivery and maintenance of essential services, and for public health measures to be implemented?
Legal issues that are highlighted in other parts of the checklist are brought together as a separate checklist here. Other issues are added.
- Identify the advantages and disadvantages of declaring a state of emergency during a pandemic.
- Each jurisdiction needs to assess the legal basis of all public health measures that are likely to be proposed, including:
* travel or movement restrictions (leaving and entering areas where infection is established);
- closure of educational institutions;
- prohibition of mass gatherings;
- isolation or quarantine of infected persons, or of persons suspected of being infected, or persons from areas where pandemic strain influenza infection is established.
- Assess standing policy on, and legal basis for, influenza vaccination of health-care workers, workers in essential services (see sections 5.1 and 5.2) or persons at high risk. Decide if this policy needs refinement to increase uptake during pandemic alert and pandemic periods. Consider the use of both seasonal and pandemic vaccine for these groups.
- Address liability, insurance and temporary licensing issues for retired health-care workers and volunteers who may be working in areas outside their training and competence in health and emergency services.
- Consider liability for unforeseen adverse events attributed to vaccine and/or antiviral drug use, especially where the licensing process for a pandemic strain vaccine has been expedited. Liability issues may affect vaccine manufacturers, the licensing authority and those who administer the vaccine.
- Ensure a legislative framework for compliance with the International Health Regulations.
- Consider including influenza or pandemic influenza in national legislation for the prevention of occupational diseases.
1.5.2 Ethical issues
Ethical issues are closely related to legal issues as mentioned above. They are part of the normative framework that is needed to assess the cultural acceptability of measures such as quarantine or selective vaccination of predefined risk groups.
Questions to be addressed
Have ethical aspects of policy decisions been considered? Is there a leading ethical framework that can be used during the response to an outbreak to balance individual and population rights?
- Consider ethical questions related to limiting the availability of a scarce resource, such as rationed diagnostic laboratory testing, pandemic strain influenza vaccine or antiviral drugs.
- Consider ethical questions related to compulsory vaccination for healthcare workers and workers from essential services.
- Consider the ethical issues related to limiting personal freedom, such as may occur with isolation and quarantine.
- Ensure the establishment of an ethical framework for research, especially when this involves human subjects.
A CBS News report showed that the U.S. went significantly further in regards to limiting individual freedom by assessing punishment and monetary penalties for quarantine non-compliance.
Federal quarantine authority is limited to diseases listed in presidential executive orders; President Bush added “novel” forms of influenza with the potential to create pandemics in Executive Order 13375. Anyone violating a quarantine order can be punished by a $250,000 fine and a one-year prison term.
This all basically constitutes a martial law takeover using the staged threat of a new flu pandemic that will coincide with the normal flu season. The CDC recently announced that they will no longer report swine flu cases. In this environment of pandemic fear, people getting sick and dying from the annual influenza strain could be initially confused for the swine flu.
So it is very clear that the vaccine could be ineffective since the fall strain hasn’t emerged yet, and it has the potential for life changing adverse reactions, or death. Since the swine flu has been relatively harmless, why are we being told to take these potentially unsafe fast tracked vaccines?
Recently, the Daily Mail reported that a scientist who advises the Government on swine flu, is a paid director of a drug firm making hundreds of millions of pounds from the pandemic.
More sinister than financial motivation, is the idea that the mass vaccination campaign is part of a depopulation agenda by the global elite. Former high level Bush Sr. insider Catherine Austin Fitts writes on her blog:
“I believe one of the goals of the swine flu vaccine is depopulation. Perhaps it is the goal of a swine flu epidemic as well, whether bio-warfare or hype around a flu season,”
This is given credence by recent reports on Infowars about mass graves ordered by FEMA officials before the pandemic flu outbreak. The UK has also ordered mass graves, inflatable mortuaries, 24 hour crematoriums, and even catacombs that were used during the cholera epidemic in 1832.
This preparation for massive deaths seems to be an exaggerated response to the recent H1N1 outbreak, unless they know something we don’t. It’s becoming fairly evident that the fast tracked vaccines could cause more deaths than the swine flu itself. We have to also consider that the vaccines themselves allow for potentially deadly strains to emerge, generating a true pandemic.
Historically, during the first year of a new presidents term, a crisis emerges that threatens the safety of the public, creates fear, and allows for the government to pose as the savior with the solution, that always amounts to more centralized control, and the erosion of civil liberties through draconian legislation.
Society cannot afford to give into fear, and set the precedent for governmental institutions to invade our bodies forcibly with untested, unsafe vaccines, without legal recourse, for a virus that has killed so few.
Gaisie Samuel is discussing. Toggle Comments
F. William Engdahl
July 20, 2009
The US Secretary of Health and Human Services, Kathleen Sebelius, has just signed a decree granting vaccine makers total legal immunity from any lawsuits that result from any new “Swine Flu” vaccine. Moreover, the $7 billion US Government fast-track program to rush vaccines onto the market in time for the Autumn flu season is being done without even normal safety testing. Is there another agenda at work in the official WHO hysteria campaign to declare so-called H1N1 virus—which has yet to be rigorously scientifically isolated, characterized and photographed with an electron microscope—the scientifically accepted procedure—a global “pandemic” threat?
With no legal liability, could it be that Baxter is preparing to sell hundreds of millions of doses containing highly toxic aluminium hydroxide as adjuvant?
The current official panic campaign over alleged Swine Flu danger is rapidly taking on the dimensions of a George Orwell science fiction novel. The document signed by Sebelius grants immunity to those making a swine flu vaccine, under the provisions of a 2006 law for public health emergencies.
Not so sage SAGE
That is once the WHO in Geneva, on recommendation of the WHO’s Strategic Advisory Group on Immunizations, declared H1N1 to be Phase 6 or Pandemic, automatic emergency health response programs could be activated even in countries such as Germany where reported outbreaks of even “suspected” H1N1 can be counted to date on the fingers of slightly more than one hand.
The WHO’s SAGE is also worth scrutiny. Its Chairman since 2005 has been the UK Director of Immunization at the British Department of Health, Dr David Salisbury. In the 1980’s Salisbury reportedly drew major fire for backing a massive vaccination of children with a multiple MMR vaccine manufactured by the predecessor company of GlaxoSmithKline. That vaccine was pulled off the market in Japan after significant numbers of children developed adverse reactions to the vaccine and the Japanese government was forced to pay significant compensation to the victims. In Sweden the MMR vaccine of GlaxoSmithKline was removed after scientists linked it to outbreaks of Crohn’s disease. Apparently that had little impact on WHO SAGE chairman Salisbury.
According to one independent UK investigator, Alan Golding, who obtained Freedom of Information documents on the case, in “1986 Trivirix, an MMR compound containing the Mumps Urabe strain AM-9, was introduced in Canada to replace MMR I. Concerns regarding the introduction of MMR in the UK are recorded in the minutes of the Joint Working Party of the British Paediatric Association and the Joint Committee on Vaccination and Immunization (JCVI) Liaison Group on June 26th of that year. Such concerns were soon to prove well grounded, as reports began to come in of an increased incidence of aseptic meningitis in vaccinated individuals. Ultimately, all MMR vaccines containing the Urabe strain of mumps were withdrawn in Canada in early 1988. This was before Urabe containing vaccines were licenced by the Department of Health for use in the UK…”
The report adds, “Smith-Kline—French, the pharmaceutical company who became Smith-Kline-Beecham and were involved in UK manufacture at that time, were concerned about these safety issues and were reluctant to obtain a UK license for their Urabe-containing vaccines. As a result of their ‘concern’ that children might be seriously damaged by one of their products, they requested that the UK government indemnify them against possible legal action that might be taken as a result of ‘losses’ associated with the vaccine, which by then was known to carry significant risk to health. The UK government, advised by Professor Salisbury and representatives from the Department of Health, in it’s enthusiasm to get a cheap MMR onto the market, agreed to this request.”
Today the same Dr Salisbury is advocating global proliferation of untested H1N1 vaccines, also manufactured by the same firm, now called GlaxoSmithKline.
The last phoney Swine Flu Disaster
The last time the US Government faced a new swine flu virus was in 1976. Thousands filed claims contending they suffered side effects from the shots. This time, the government has taken steps to prevent any possible legal remedy should thousands of US citizens suffer severe complications as a result of being given untested vaccines.
In 1976 President Gerald Ford, facing a difficult re-election campaign, was advised by the head of the CDC, David Sencer, to launch a mass national vaccination. As today with H1N1 Swine Flu, Sencer also used the scare of the alleged 1918 flu pandemic. Notably, some scientific researchers maintain that the deaths during the flu wave of 1918-1919, in the aftermath of the ghastly First World War, came not from any virus but from the governmental campaigns of mass vaccination against “Spanish Flu.” Interestingly, the Rockefeller University and Foundation was in the middle of that event as well.
Cases of what was then called swine flu were found in soldiers at Fort Dix, N.J. in 1976, including one death. That death, whose true cause is in dispute as the soldier, sick with influenza was put on a forced march despite and fell dead, was used by Sencer to convince Ford to launch one of the most infamous public health fiascos in US history, forcing Sencer’s resignation as CDC head. Federal officials vaccinated 40 million Americans during a national campaign. A pandemic never materialized, but thousands who got the shots filed injury claims, as they contracted a paralyzing condition called Guillain-Barre Syndrome or other side effects. At least 25 people died after receiving the vaccine died and 500 developed Guillain-Barre syndrome, an inflammation of the nervous system which can cause paralysis and be fatal. The US Government was forced to pay damages after vaccination victims made it a national scandal. In the end the 1976 Swine Flu vaccine proved far worse than the disease.
Sencer was fired in 1977 for the fiasco but by then the damage had already been done.
No Safety Test? Don’t worry, be happy…
The story gets worse. Now that the Obama Administration has signed a document of immunity from legal prosecution, the FDA in the United States and UK health authorities have decided to let Big Pharma put vaccine products onto the market before any tests of the possible harmful side effects of the vaccines are even known.
The first doses of swine flu vaccine will be given to the public before full data on its safety and effectiveness become available. The untested “pandemic” vaccines will be spread over two doses in a higher quantity, and one brand reportedly will contain a chemical additive, an adjuvant, to make it “go further,” dramatically potentially increasing the risk of side-effects.
Children will be among those first in line for the shots and may get the vaccine more than a month before trial results are received.
In the UK the government’s National Health Service, NHS, has been ordered to plan for a worst-case scenario in which swine flu might cause 65,000 deaths over the coming winter, including several thousand deaths among children.
The British Government has placed advance orders for 132 million doses of vaccine with two manufacturers, GlaxoSmithKline and Baxter, who have licensed “in advance” three “core” vaccines in preparation for a pandemic, conveniently enough even though we are told by WHO and epidemiologists that we cannot prepare in advance for what could be a more ominous mutation of the currently very mild H1N1 problem.
Curiously enough, a full year before any reported case of the current alleged H1N1, the major pharmaceutical company, Baxter, filed for a patent for H1N1 vaccine: Baxter Vaccine Patent Application US 2009/0060950 A1. Their application states, “the composition or vaccine comprises more than one antigen…..such as influenza A and influenza B in particular selected from of one or more of the human H1N1, H2N2, H3N2, H5N1, H7N7, H1N2, H9N2, H7N2, H7N3, H10N7 subtypes, of the pig flu H1N1, H1N2, H3N1 and H3N2 subtypes, of the dog or horse flu H7N7, H3N8 subtypes or of the avian H5N1, H7N2, H1N7, H7N3, H13N6, H5N9, H11N6, H3N8, H9N2, H5N2, H4N8, H10N7, H2N2, H8N4, H14N5, H6N5, H12N5 subtypes.”
The application further states, “Suitable adjuvants can be selected from mineral gels, aluminium hydroxide, surface active substances, lysolecithin, pluronic polyols, polyanions or oil emulsions such as water in oil or oil in water, or a combination thereof. Of course the selection of the adjuvant depends on the intended use. E.g. toxicity may depend on the destined subject organism and can vary from no toxicity to high toxicity.”
With no legal liability, could it be that Baxter is preparing to sell hundreds of millions of doses containing highly toxic aluminium hydroxide as adjuvant? Perhaps it is time to demand that all leading officials of WHO, SAGE and CDC, the US Obama Administration, Cabinet officials and members of Congress w, the US Obama Administration, Cabinet officials and members of Congress who voted the $7 billion H1N1 emergency funds and who have gone along with the declaration of pharmaceutical company immunity from subsequent prosecution for damage from their products. The same should apply as well for other national health bodies demanding its citizens take the H1N1 vaccine from GlaxoSmithKline or Baxter to see if it is really safe.
And WHO stopped even tracking H1N1
Another indication that the world is being taken for colossal suckers in the entire WHO Swine Flu scare scenario, the WHO itself, the world body entrusted to monitor outbreaks of so-called pandemics or even epidemics worldwide, has just decided to stop tracking Swine Flu or H1N1 Influenza A as they prefer to name it now, so as not to offend Smithfield Foods and other industrialized pig CAFO producers.
The World Health Organization in a “briefing note” posted on their Web site posted the baffling notice that they would no longer track outbreaks of H1N1. The last WHO update, issued July 6, showed 94,512 confirmed cases in 122 countries, with 429 deaths. The WHO apparently claims that the numbers of laboratory-confirmed cases were actually meaningless.
The briefing note said countries would still be asked to report their first few confirmed cases. It also said countries should watch for clusters of fatalities, which could indicate the virus had mutated to a more lethal form. Other “signals to be vigilant for,” it said, were spikes in school absenteeism and surges in hospital visits. The Atlanta CDC has also agreed to the WHO count drop. Dr. Michael T. Osterholm, director of the Center for Infectious Disease Research and Policy at the University of Minnesota, admits that the existing tests to confirm H1N1 Influenza A are not even certain, but rather hit-or-miss. “Bad measures can be worse than no measures at all,” he stated. So the WHO has decided to drop tests that anyway did not give a scientific picture of who had H1N1 or not, and as well they have decided to drop counting any test results or cases of H1n1 around the world with the comment that “we can assume almost all cases are H1N1 Swine Flu. This is science on which basis we are told to vaccinate our young? Whoah there…Not with our children.