Natural Solutions Foundation suing FDA to prevent release of Swine Flu vaccines. We’ll be entering our papers this week. We are restricting our suit to a narrow objection although we know that the vaccines are genocidal (see below) and worse. But we have to use what the law gives us and that is the fact that the law was broken on September 15, 2009 when the vaccines were licensed without any safety testing being completed (or even carried out).
Be aware that we are not satisfied with a mere delay, but it is where we start tactically. Winning this suit would prevent the release of the vaccines until next June or July, 2010. That is not shabby since it would give us time for more permanent action.
Federal Court Cases are expensive! Please make two recurring tax deductible donations, large or small: Click here, http://drrimatruthreports.com/?page_id=189, to make a donation ending in the number 6 to earmark you donation for the legal case. Now click the link again and make a donation ending in any other number to support the Natural Solutions Foundation so we can continue to serve you and help keep health freedom free. Thanks!
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OK. Now for the tough stuff
The article below details the horrific reality that I wish were not true. The Natural Solutions Foundation has been saying for quite some time that we see clear evidence of a genocidal intention in the overblown, clearly intentional Swine Flu “Pandemic”. When WHO moved the “Pandemic” from Level 4 to Level 5 the disease was so mild and inconsequential that they literally had to change the definition of a Pandemic at Level 5, leaving out the words “with the ability to cause serious illness and death” from the definition because it did not and could not. We believe that this must have been a great disappointment to the folks at the WHO who have been both predicting and involved with genetically engineering one failed pandemic after another. But WHO, you will remember, believes in a “sustainable planet” and that sustainability (favor them, not us, of course) means that they believe, too, that 90% of the world’s population needs to die.
They do not much care how we die as long as we do it on demand and they manage to squeeze out a good dollop of profit as we do so. Some of us, however, will die because we are never born. That, too, is part of the genocidal plan. You may recall that we reported some time back that we had seen official WHO documents from 1985 stating that the real purpose of the current vaccination program taking place in Africa at that time was not disease control (they know perfectly well that vaccines are hokum, without a shred of valid scientific evidence behind them) or prevention, but the dissemination of materials which cause infertility in the women into whom it is injected. At that time, they were using vaccines with strong response patterns laced with Human Chorionic Gonadotrophin (HCG), a reproductive hormone (a glycoprotein, by the way – that figures into this true horror story a little later on). When you train the immune system through injecting it with adjuvants to “break tolerance” or attack the molecules as “not me” that it normally recognizes as “me”, if you prime it properly, you can create an immune intolerance to the hormones or other molecules of your own body.
In this case, and the same system has been used against untold millions (billions?) of women in many third world countries all over the world, the body attacks every molecule of HCG it encounters after that. The problem is that without HCG, the uterus cannot retain the embryo, or the fetus and it will expel the future baby if she were pregnant at the time of the injection. If she were not pregnant, she will never again become a mother. Her body now destroys the very hormone without which she cannot sustain a pregnancy. This damage is irreversible.
But not universal. Apparently, that is the problem: there are still a few people whose immune response is not sufficient to destroy all of their fertility. So now we move, in the march of mad science, propelled by forces of such deep inhumanity that it is difficulty to confront them with clear, calm eyes, to another infertility system.
In 1998 a Patent Application was made for a system which uses a person’s own immune system to render them permanently infertile, sterile, unable to have children. The system is irreversible, once injected.
– Both Novartis and GSK vaccines “against” the trivial Swine Flu both contain 1 million times more squalene than the devastatingly dangerous Vaccine A which crippled and killed so many Gulf War I military personnel (See Squalene: Be Very Afraid Part I, http://drrimatruthreports.com/?p=3592)
– Even a few molecules of squalene injected into the body causes it to “break tolerance” and attack the body’s own molecules to which it is now trained for attack, including the body’s own squalene, a vital component of the Central Nervous System (which accounts for the profound and cataclysmic neurological symptoms of squalene injection
– The WHO, UN and US governments agree on the “need” to reduce population to only 10% of its current levels
– When the WHO declared a Level 6 Pandemic on June 11, offical control of the political and health functions of all 194 countries in the WHO passed to that body, per an agreement signed in 2005 which took effect in 2007
– The haste with which this Level 6 Pandemic was declared makes it clear that the agenda was agreed to whether or not the genetically engineered virus did its job
– FDA/CDC has said that the $1/2 billion stock pile of injectable squalene adjuvant which the US Government admitted it was stock piling will be used to add the squalene to the bodies of people receiving the vaccines which do NOT have adjuvants in them at the time of injection
– The patents for a glycoprotein-containing, squalene adjuvanted H1N1 vaccine were filed in 2007 and 2008 by Novartis, Baxter International and GSK despite the fact that the virus did not yet officially exist, there had never been approval of a squalene adjuvanted vaccine and use of squalene in mass vaccines was illegal through the permanent restraining order of Judge Emmett Sullivan and through the fact that squalene was forbidden to even be tested in the US. The investment of billions of dollars into the development of these vaccines for a virus that did not yet exist, using substances which had never been approved for use in vaccines by 3 separate companies, allegedly competitors in the vaccine industry, is worthy of note all by itself
– The most vulnerable members of society, children and pregnant women, will be vaccinated first.
Now you know what the game is. Since the goal is infertility, what better target population could you choose? With one fell swoop of a needle, a whole generation of “useless eaters” is wiped off the map – the next one while this one is too sick to make much trouble and you clean up like the bandit that you are, if, of course, you are Big Pharma and the global genocidalists!
So now we have mandates for “Influenza vaccines” which are designed to roll the “Swine Flu” up under them. Understand clearly that although your State may offer you exemptions for philosophical, religious or medical reasons, there is every liklihood that there will be NO pandemic vaccination exemptions. The way the federal and state regulations are reading right now, that is the situation. The confusers really do want you to feel
– All vaccinations will be voluntary for the pandemic flu. This is true if by voluntary you really mean “under duress and pain of incarceration, fine and imprisonment.”
– Conventional exemptions will hold for the pandemic flu. This is not true. The pandemic vaccine is governed by separate regulations and laws which do not allow for exemptions.
– Parents will be given the choice of whether to vaccinate their children and themselves or not. This is utterly false unless we take back our freedom to make these decisions for ourselves and our children. Experimental medical procedures are never carried out on the most vulnerable and defenseless first, not until now, that is.
As an aside, do you suppose that President Obama’s children will get the same vaccine that yours and mine will? How would we know? How about the President himself, who bravely agreed to wait until near the bottom of the list. How courageous and public spirited. I will be happy to join him below the bottom of the list and, if all of us have any sense at all, we will all do so by making it abundantly clear to our legislators that this WILL not happen. That is the purpose of the action item, http://salsa.democracyinaction.org/o/568/campaign.jsp?campaign_KEY=27275. So far more than 2,222,940 of your emails have reached the legislative and decision making desks of this country. These people need to hear that the deception is broken, like immune tolerance when adjuvants are injected. We want the right to determine what happens to our bodies. We will not be sickened and die for the depopulationists. We will not be made infertile for the neo-aristocrats. We will not be brought into slavery through a diabolical brew in a syringe of illness, infertility and death..
Now, please read the following article and share it widely while you take the time and effort to mobilize every single person you can reach to help mobilize the groundswell to make it impossible for the vaccine effort to go forward as intended.
Daniel Solis from the Czech Republic has researched the side-effects of the adjuvant, squalene, and discovered it is known to destroy fertility as well as causing other forms of damage.
A patent for a vaccine to impair fertility in animals contains squalene.
The plan to use this fertility-impairing adjuvant in the “swine flu” vaccine against a flu that has so far been far less irksome than the ordinary seasonal flu underscores concerns that this H1N1 mass vaccination programme mandated by WHO with the support of pharma companies such as Baxter is designed primarily to cause death and injury, and so significantly reduce the global population.
Is it any wonder that these “vaccines” are classified as bioweapons by the regulators? ….
Daniel Solis has also made a formal complaint against the head of the Czech Republic’s FDA and the Deputy Health Minister for awarding a contract to Baxter worth 1,5 billion CZK without an open tender. More legal action in the Czech Republic is planned with the aim of getting Baxter’s license to manufacture the “swine flu” vaccine at Bohumil suspended and to make Baxter accountable for the incident at the BioTest lab, which detected the live bird flu virus in vaccine material from Baxter on February 6th. Members of the lab had to be treated preventatively for bird flu and were put in quarantine.
“I have focused on the adjuvants made of monophosforyl lipid A (MPL) MF59TM (containing a polysorbate TweenTM 80) or AS03, AS04 also known as squalene in the proposed vaccines, which are immunosterilant or an immunocontraceptive,” Daniel Solis writes.
“The patent of the veterinary FERTILITY IMPAIRING VACCINE can be found on-line. It mentions both, the lipoid adjuvants squalene and the polysorbate TM80.
Here are the quotes from the patent and further some clinical studies about the toxicity of both.
(WO/1999/034825) FERTILITY IMPAIRING VACCINE AND METHOD OF USE
This application claims the benefit of U. S. Provisional Application No. 60/070,375, filed January 2,1998, U. S. Provisional Application No. 60/071,406, filed January 15,1998
“The vaccine of the invention preferably additionally includes an immunological adjuvant to enhance the immunological response of the subject to the glycoprotein antigen. Examples of adjuvants include Freund’s Complete Adjuvant, Freund’s Incomplete Adjuvant, and an adjuvant comprising an immunostimulant such as synthetic trehalose dicorynomycolate (STDCM) and an oil such as squalene oil (see P. Willis et al., J. Equine Vet. Sci., 14,364-370 (1994)). An adjuvant comprising synthetic trehalose dicorynemycolate, squalene oil, and a surfactant such as lecithin is preferred. Lecithin typically includes phosphatidyl choline. In a preferred embodiment the vaccine comprises oil, preferably a biodegradable oil such as squalene oil. Typically, the vaccine is prepared using an adjuvant concentrate which contains lecithin in squalene oil. The aqueous solution glycoprotein is typically a phosphate-buffered saline (PBS) solution, and additionally preferably contains Tween 80.”
A vaccine comprising an antigen derived from a zona pellucida glycoprotein is effective to impair fertility in animals, preferably carnivores. The vaccine can be used as an immunosterilant or an immunocontraceptive.
Annals of Allergy, Asthma and Immunology, Volume 95, Number 6, December 2005 , pp. 593-599(7)
“Polysorbate 80 was identified as the causative agent for the anaphylactoid reaction of nonimmunologic origin in the patient. Conclusions: Polysorbate 80 is a ubiquitously used solubilizing agent that can cause severe nonimmunologic anaphylactoid reactions.”
Gajdova M, Jakubovsky J, Valky J.
Institute of Preventive and Clinical Medicine, Limbová, Bratislava.
Delayed effects of neonatal exposure to Tween 80 on female reproductive organs in rats. Food Chem Toxicol. 1993 Mar;31(3):183-90. PMID: 8473002.
“Baby female rats were injected with polysorbate 80 at days 4-7 after birth. It accelerated the maturing of the rats and caused changes to the vagina and womb lining, hormonal changes, ovary deformities and degenerative follicles.” http://www.ncbi.nlm.nih.gov/pubmed/8473002
The Endogenous Adjuvant Squalene Can Induce a Chronic T-Cell-Mediated Arthritis in Rats
Barbro C. Carlson*, Åsa M. Jansson*, Anders Larsson, Anders Bucht and Johnny C. Lorentzen* http://ajp.amjpathol.org/cgi/content/abstract/156/6/2057
“Dr. Jules Freund creator of this oil-based adjuvant warned in 1956 that animals injected with his formulation developed terrible, incurable conditions: allergic aspermatogenesis (stoppage of sperm production), experimental allergic encephalomyelitis (the animal version of MS), allergic neuritis (inflammation of the nerves that can lead to paralysis) and other severe autoimmune disorders.
Source: : Gary Matsumoto, Vaccine A-The Covert Government Experiment That’s Killing our Soldiers and Why GI’s are Only the First Victims, Kapitola 3. “The Greatest Story Never Told” http://www.vaccine-a.com/excerpt.html”
September 16, 2009 – URGENT NOTE: Your Action Required Now to Secure Your Right to Refuse the Swine Flu Vaccine Without Incarceration
Health Freedom’s best friend in Congress has responded to our Push Back. We’ve sent more than 2 million emails demanding the right to say “NO!” to vaccines without punishment, incarceration or involuntary quarantine. The Congressman knows how important that is to health, liberty and, we have to imagine, sanity. We have been in discussion with his office about introducing a bill modeled on our Draft Legislation to prevent pandemic vaccination which is mandatory, compulsory or taken under duress of any type.
We received a call today from the Congressman’s office telling us that he is close to introducing a new No Compulsory Vaccine Bill to the House. Given the fact that we have sent well over 2 million emails to our State and Federal legislators, HHS Secretary Sebelius, DHS Secretary Napolitano, President Obama and the Governors of every State in the Union, we anticipate that his bill will garner a good deal of support.
NOW IS THE TIME TO TURN UP THE HEAT. WE NEED 2 MILLION MORE EMAILS IN THE NEXT WEEK. CAN WE DO IT? YOU KNOW WE CAN! WE ARE THE NET ROOTS OF HEALTH FREEDOM!
Have you already sent this Action Item once for every member of your household demanding the right to self shield instead of facing mock-voluntary Swine Flu vaccination with incarceration as the consequence of vaccine refusal? If so, thank you. If not, now, more than ever, we need your help in taking this action right now. We need every bit of support we can muster. Once we get Dr. Paul’s bill number and text, we will publish it and then we’ll ask you to do the same thing again: click on the link we’ll give you to support that Action Item as if your life depended upon it. It will.
And don’t forget that we are 100% supporter supported.
Please set up two (2) recurring donations, whether large or small: one tax deductible donation to support our legal challenge of the legality of the FDA’s approval of the vaccines Secretary Sebelius is referring to in her testimony below. That one should end in the number 6 to ear mark it for our legal fund. The other tax deductible donation can end in any number and it keeps the Natural Solutions Foundation keeping-on. Here is the link: http://drrimatruthreports.com/?page_id=189
Now, on to the all too real, but still very surreal, testimony authorizing the Pandemic Swine Flu vaccines without any, that’s right, any safety testing. On September 15, 2009, a terrible, tragic and tyrannical event in America’s history took place. HHS Secretary Kathleen Sebelius testified before the US House of Representatives Committee on Energy and Commerce and, in that testimony, announced the “licensing” of the “Swine Flu” vaccines. Secretary Sebelius, please allow me to remind you that it is a crime to provide false testimony before Congress.
I was not in the chamber when the Secretary announced the approval of several Swine Flu vaccines using a combination of untruth, falsehood, illogic and deceit. But I would like to present my virtual interview of Secretary Sebelius as she reads her testimony before that Committee and I question her about it. Remember that every word following SKS (Secretary Kathleen Sebelius) is her unedited testimony, with nothing altered or changed in context. I guess she is counting on the declining quality of the educational system in the US to see her through.
Watch for the new Youtube.com.naturalsolutions series in which Secretary Sebelius and I have a virtual interview. Here is the text of that virtual interview. Please read and share as widely as you can.
A virtual Interview with Secretary Sebelius on the “Swine Flu” Vaccine Licensing
My comments are in italics, labeled “REL”
Secretary Sebelius’ comments are labeled SKS.
SKS: Preparing for the 2009-2010 Influenza Season
Secretary of Health and Human Services Kathleen Sebelius
Secretary, U.S. Department of Health and Human Services
SKS: Chairman Waxman, Ranking Member Barton, Chairman Emeritus Dingell, members of the Committee, thank you for this opportunity to update you on the public health challenges of 2009 H1N1 influenza. I want to assure the Committee that the Administration is taking these challenges seriously…
REL: These challenges do not exist, Secretary Sebelius. They have been manufactured as a kind of, at best, a cynical windfall of unprecedented proportions for Big Pharma. At worst, you and your conspirators are playing Doctor Death with America, starting with our next generation, children and pregnant mothers.
SKS: and has mounted an aggressive plan to address H1N1 throughout this fall and winter.
REL: The challenges you speak of do not exist. Without any challenge, an aggressive plan is totally unnecessary.
SKS: HHS has a leading role because this is a health event, and we are working in close partnership with virtually every part of the federal government under a national preparedness and response framework for action that builds on the efforts and lessons learned from this spring. Working together with governors, mayors, tribal leaders, state and local health departments, the medical community and our private sector partners, the federal government has been actively preparing for possible H1N1 virus outbreak scenarios that may develop over the next few months.
REL: Madam Secretary, you are saying “MAY develop” but your use of the phrase, “MAY DEVELOP” shows there is no sufficient scientific evidence that the so-called “Swine Flu” is a pandemic threat. You have called it a “novel” virus, which is a condition for there to be a pandemic potential, but you are not treating this vaccine as thought it were a novel vaccine, requiring safety testing. Given the costs in human and financial terms, I am afraid that “MAY DEVELOP” is not sufficient for vaccination of the population, starting with our most vulnerable population.
SKS: Since the initial spring outbreak of 2009 H1N1 influenza, the virus has triggered a worldwide pandemic,
REL: Well, no. Actually a world wide pandemic has been declared without any clear evidence that there actually IS a world wide pandemic. There is NO world-wide pandemic; there is a only legally declared pandemic, made possible only because the W.H.O. changed the definition of a “pandemic” for political reasons. The “pandemic” has been declared without any clear evidence that there is any world-wide threat. How has the Secretary ascertained, in the absence of accurate testing, that H1N1 is the “DOMINANT” flu strain? Australian authorities do not confirm your claim.
SKS: and has been the dominant flu strain in the southern hemisphere during its winter flu season.
REL: Just how is this ascertained in the absence of accurate testing, not just testing, mind you, but accurate testing that H1N1 is the “DOMINANT” flu strain? Australian authorities do not agree with or substantiate your claim.
SKS: The evidence to date shows that the virus has not changed to become more deadly.
REL: At last, Madam Secretary, we have common ground. We agree, and therefore, since both WHO and CDC has said that this H1N1 virus causes a disease that is milder than seasonal flu, requiring no medical intervention, why is major medical intervention required for something that poses no dangers and may, MAY, become a problem at some time, somewhere in the future?
I am sorry, Madam Secretary, but this is absurd, unscientific, dangerous and a ferocious waste of money, sort of like TARP and other corporate welfare programs, but this time for Big Pharma.
SKS: Unlike our typical seasonal flu, we continued to see flu activity in the United States over the summer, notably in summer camps.
REL: But since diagnosis is not being carried out, is it Swine Flu? Allergies to GMO junk food fed to children, perhaps, common colds, maybe? How would you know? The best tests we have are wrong 9 times out of 10. WHO and CDC requested countries not to test for the virus and not to keep accurate counts, just to guess – and it is on these guesses that you apparently are making your pronouncements, judgments and decisions.
SKS: More recently, we have seen an increase in 2009 H1N1 influenza activity in several states
REL: Based on what independently verified data? If you have no lab tests, you would have no idea of what you are seeing.
SKS: and expect this to continue across the United States during the coming months.
REL: All respiratory cases are being assigned the unscientific label of “Swine Flu” without testing. No one has any idea if any of these cases are causes by H1N1, except, apparently you, Secretary Sebelius. Assuming, however, that all of them are, there are no deaths which are not caused by underlying disease or treatments with toxic, but approved drugs such as Tamiflu, which killed a pregnant mother and the baby she gave birth to in Mumbai, India recently.
Diagnosis by symptom picture alone. Right. That is not exactly good science and it certainly is terrible medicine. Swine Flu walks like a duck, coughs like a duck and has a fever like a duck. What makes it a swine? Public relations and nothing else!
SKS: As fall begins, we anticipate that even more communities may be affected than those that saw cases this past spring and summer.
REL: Again I ask you, Secretary, based on exactly, precisely, what?”
SKS: In addition, communities may be more severely affected, reflecting wider transmission and causing potentially greater impact.
REL: I am afraid I have to ask again, based on what? You say that communities may be more severely affected, but the truth is that they may also be less severely affected. Where do you get your crystal ball serviced, Madam Secretary? Could it be the same place that Novartis used when they decided to patent a vaccine for the Swine Flu in 2008 when CDC and WHO declare that this is a novel, never-before-seen virus which arose, de novo, like Athena from the forehead of Zeus, in April, 2009? Could the same shop be servicing Baxter’s decision-making Magic 8 Ball so that they were able to apply for a patent for a Swine Flu vaccine in 2007? If so, Madam Secretary, this crystal ball is a national treasure and should be made available to “We the People of These United States.”
SKS: Seasonal influenza viruses may cause illness concurrently with 2009 H1N1 this fall and winter and it will not be possible to determine quickly if ill individuals have 2009 H1N1 influenza, seasonal influenza, or other respiratory conditions based on symptoms alone.
REL: It may. Or, then again, it may not. There is no hard data on which to make these predictions and the consequences of these predictions, including vaccines are dangerous and unwarranted by any level of fact or reality. I repeat, there is simply no hard data, or at least none that you have presented on your websites, public statements, press releases or here today.
SKS: It is also difficult to predict the severity of the disease that we will see in the coming months from either 2009 H1N1 or seasonal influenza.
REL: Right again, Madam Secretary. So why poison the populace for something whose dreadful menace did not materialize and is not showing any signs of materializing. In fact, its dreadful menace is a lot like the bogyman under the bed: a product of your big brother’s desire to scare you witless so that you will do whatever he says. The parallel is uncanny.
SKS: Influenza is an unpredictable disease and we know that things will change and we will learn more throughout the fall.
REL: So unpredictable, in fact, that seasonal flu vaccines are accurate less than 40% of the time although the toxins injected (mercury, aluminum, formaldehyde, foreign protein, MSG, etc., fluoride, etc.) are toxic 100% of the time and become more so with more shots, which are increasingly r4commended by conflict-of-interest-laden ACIP (Advisory Committee on Immunization Practices) and others of their stripe. By the way, Secretary Sebelius, what is your financial interest in the medical and pharmaceutical industries?
SKS: Shared Responsibility and Science-Based Guidance Slowing the spread and reducing the impact of H1N1…
REL: From nothing to nothing?
SKS: …and seasonal flu is a shared responsibility…
REL: Exactly what does that mean? There is no meaningful impact from H1N1, but there certainly will be from yet another round of vaccines, even if those vaccines are, as falsely stated, but a strain change variation on a theme. Children vaccinated with attenuated live virus vaccines, specifically influenza vaccines, are many times more likely to be admitted to hospitals for all causes, many times more likely to develop serious asthma, etc. There is nothing trivial about influenza shots but, with the guidance of ACIP they are increasingly passed out as if they were either safe or effective. In fact they are neither and, if it is merely a strain change variation, then H1N1 is also neither safe nor effective. It it is a novel vaccine for a novel virus, it is clearly neither safe nor effective since it has never had any safety testing concluded. Were such safety testing to show that it were not safe or effective, then the sales and administration of it would pierce the veil of liability free manufacture, distribution and use which the Federal government has accorded to itself, its agents and to the manufacturers and distributors of these dangerous vaccines as we.. It is therefore in the ir best interest not to have any safety data (or data showing the lack of safety).
SKS: …and we all need to plan for what would need to be done when the flu impacts our community, school, business or home this fall.
REL: When? Shouldn’t the word be “IF” or “just in case” or “In the unlikely chance that it might, given the lack of evidence that it can”?
SKS: Given that flu already is circulating in the United States this fall, it’s important for every American family and business to prepare their own household and business plans and think through the steps they will have to take if a family member or co-worker contracts the flu.
REL: Tuberculosis is also circulating this fall. So are impetigo, gonorrhea, athlete’s foot, head lice and zits. Is the US Government offering a TARP bailout, at the expense of our lives, to the the very wealthy, very powerful Pharmaceutical Industry?
SKS: CDC has provided specific recommendations for what individuals, communities, clinicians, and other professionals can do.
REL: In the face of trivial disease, if it indeed exists in community distribution, for which there is no evidence that has forensic or scientific credibility, these common sense wash-yours-hands, cover your mouth and nose when you sneeze recommendations are more than sufficient the help out a perfectly unthreatened population. My mother taught me that, too, and it sufficed.
SKS: Individuals can take actions to prevent respiratory infections. We emphasize frequent hand-washing as an effective way to reduce transmission of disease. It is very important for sick individuals to stay at home,
REL: Really? Do employers know that and do they refrain from docking them?
SKS: and for parents to keep children who have a fever or flu-like illness home from school, childcare, the playground, or other places children gather.
REL: Flu is not necessarily Swine Flu.
SKS: Similarly, sick individuals should not get on an airplane or any public transport.
REL:This benign-sounding provision will result in persons who have not been vaccinated being denied boarding privileges on public transport in the United States unless we stop this medical fascism now. There is already talk of stainless steel RFID chipped bracelets at state trooper checkpoints. Where accurate or not, this suggestion illustrates how easily this type of tyranny would be to install. Tyrannical control never presents itself as that. it always wants to help, to take care of, to protect you. This process of constitutional abrogation, so well advanced at the state and federal levels, is receiving another set of supporting members in this document, Madam Secretary, and in this dangerous and unwarranted approval.
SKS: Taking personal responsibility for these things will help reduce the spread of this new virus as well as other respiratory illnesses.
We have issued new guidance from the CDC on www.flu.gov for schools, child care settings, colleges and universities, and large and small businesses that also includes strategies for preventing the spread of flu, especially in the early fall when the 2009 H1N1 vaccine will not yet be ready. These comprehensive guidelines provide advice on how individuals and institutions can guard against the flu and mitigate its spread. The CDC also has issued guidance for healthcare providers about appropriate use of anti-viral drugs to treat patients who are at highest risk from complications from the seasonal and 2009 H1N1 flu.
REL: These guidelines offer dangerous pharmacological usage practices which, like the vaccine approval itself, is not supported by science. In fact, the science of the antivirals suggests very strongly that they should not be used and their use, while increasing the liklihood of serious complications and death, does little or nothing to shorten or minimize the severity of the purported “Swine Flu” infection. Remember, it can only be purported because the laboratory testing is not being done, based on the recommendations of the CDC and W.H.O. Why? Because the testing is so inaccurate. Therefore any suggestion about incidence, prevalence or impact is mere fantasy. Tamiflu and Relenza have not been shown to bring about positive outcomes in this diagnostic fantasy matrix, in fact, quite the contrary.
SKS: Additional work is being done on critical guidelines to address infection control and worker safety in healthcare settings. Our recommendations and action plans are based on the best scientific information…
REL: Please refer to what I have said above and my comments below, Madam Secretary.
SKS: …available to help our nation respond aggressively and effectively to the 2009 H1N1 virus.
REL: This may sound awfully familiar by now, Madam Secretary, but why? Where is the justification for aggressive action or the demonstration that effective action is not achieved by the “Personal responsibility” suggestions and by the protection of the collective immune system through avoiding junk foods, chemicals, GMOs and other health degradation substances and processes permitted by your agency, the same FDA which is now so sanctimoniously declaring its benign intent here?
In fact, the same FDA has literally criminalized communications which offer non-vaccine, non-drug options to prevent, treat, mitigate or cure the Swine Flu. It is hard to see how the FDA is working to help our nation respond aggressively and effectively to anything except the need to make the population docile, obedient, sick and profitable in its chronic illness.
SKS: We are working to ensure that Americans are informed and consistently updated with information in clear language. This is a dynamic situation, but it is essential that the American people are fully engaged so they can be part of the response.
REL: Really? To my mind, being fully engaged would require clear, accurate information and, I am very much afraid that your testimony makes it clear that the intention of the FDA is to provide anything but that. You are providing information in easily understood words, but it is distorted and dangerous. If your FDA were interested in that goal, it would be offering abundant information on nutrition, antioxidants, homeopathy, Foods, nutrients, nano silver and supplements designed to support the immune system.
SKS: The federal government, particularly the CDC, will be conducting weekly and, when necessary, daily briefings that will be available at flu.gov to get critical information out to the American people.
Vaccination Campaign The federal government is also preparing for a voluntary national vaccination campaign for the 2009 H1N1 virus starting in October.
REL:The Federal Government has backed off from its earlier stance for mandatory vaccination, which was articulated by HHS on July 23, 2008 and by DHS on the following day in advisory communications.
SKS: With unprecedented speed, we have completed key steps in the vaccine development process — we have characterized the virus, identified a candidate strain, expedited manufacturing, and performed clinical trials.
REL: Clinical trials have not been performed. Brief dose response trials have been initiated, is some cases not even completed before this authorization.
SKS: The speed of this vaccine development was possible due to the investments made through ASPR/BARDA over the past six years in advanced research and development and infrastructure building.
REL: How convenient!
SKS: One-hundred ninety-five (195) million doses of H1N1 vaccine have been purchased from five manufacturers by the U.S. government.
REL:Vaccines have already been purchased, BEFORE their approval? That makes their approval sound very much as if it were pre arraigned. Why the haste? Why the collusion? Your agency declared a national state of health emergency on April 25, 2009, just 11 days after the first so-called death from the so-called novel virus in Mexico. A level 6 pandemic was declared on June 11, just shy of 2 months after the first alleged death. The death toll was reduced in Mexico from 168 to 16, a percentage decrease in mortality of 90.5%. This miracle of biblical proportions was not only ignored, but the decrease in observed mortality was apparently not factored into the response of either WHO or FDA.
SKS: Two types of vaccine will be available: vaccine made from killed virus for injection (flu shot) and vaccine with live, weakened virus administered by nasal spray.
REL: Madam Secretary, our information is that this is simply not correct. We have been informed that there is more than one inactivated live virus preparation. We are checking this out now.
SKS: The vaccines are being manufactured by the same methods used for the production of the seasonal flu vaccines administered every year.
REL: I am afraid that this is simply not true. Conventional influenza vaccines are cultured in eggs. Cell based, rather than egg based, vaccines are not the norm and are not just a simple “strain change” variation of the same old vaccine. MF59, and oil and water adjuvant, is not the norm. The virus is said by both WHO and FDA to be unpredictable and to be a totally novel virus. In that case, there is no possibility that all approved vaccines are merely strain change variations on a well proven, but not particularly safe, theme. FDA can only have it one way or the other, but not both, Madam Secretary.
SKS: NIH is conducting a series of clinical trials on the vaccine to determine the safety and number of doses needed to induce a protective immune response.
REL: Safety trials will not, according to the FDA< be completed until June, 2010. Approval of the novel vaccines before that point constitutes irresponsible dereliction of duty at the very least. Since full disclosure and informed consent are not possible under the conditions of secrecy which prevail in these tests, it is possible that they are illegal and that they constitute crimes against humanity.
SKS: Trials in healthy adults and the elderly began in the first week of August. Complete immune response data from the first trials—those studying two doses in healthy adults—are expected in late October.
REL: The approval of 5 different vaccines was announced today, September 15, 2009. There is no possibility that even the preliminary dosage trials in healthy adults have been completed. No trials in immuno compromised or suppressed people, vaccine injured persons, infants, people with atopic disorders like asthma, eczema, egg allergies, organ transplant recipients, cancer chemotherapy patients or those on steroids, etc., have been conducted. No safety information exists to guide usage or administration. This is consistent with the lack of information which would pierce the veil of liability protection as mentioned before.
SKS: Preliminary data indicate that the vaccines are safe
REL: What preliminary data. Is that sufficient to jeopardize the health of a nation for a non existent threat of a disease?
SKS: and that a single 15-microgram dose induces what is likely to be a protective immune response in healthy adults between the ages of 18 and 64.
REL: We should note that no one says that the dose will be protective since vaccines have never been shown to be protective of diseases for which they are administered. Not a single double blind, placebo controlled study on this question has ever been done. But the antibody production generated by vaccines is assumed, not know, to provide protection. Given the dangerous nature of these novel vaccines for a novel virus, don’t ou think, Madam Secretary, that more information about the conclusive results of carefully designed safety testing, with fully informed consent, would be in order before these vaccines were approved?
SKS: For adults aged 65 and over, the preliminary data indicate that the immune response to the 2009 H1N1 influenza vaccine is somewhat less robust, as is the case with seasonal influenza vaccine.
REL: And there is no intermediate or long term safety data on the adjuvanted vaccines whatsoever since no adjuvanted vaccine has ever been approved before in the US. the only two adjuvanted vaccines available in Europe are for patients on dialysis, whose immune function is so suppressed that they are deemed to need the extra “punch” of the squalene adjuvant and, according tot he controlling agency, have such a reduced life span that they are not expected to live long enough to develop side effects and complications from the vaccine and Cervavax, GSK’s competitor to Garadsil, the HPV vaccine.
Parents who continue to state that their daughters were either killed by, or seriously damaged by Cervavax administration are being warned that if they continue to disseminate that information their children will be taken from them.
The suggestions in this data is that although dangerous, the danger is being hidden. Without a good deal of further clarification, the approval of adjuvanted vaccines, or the potential administration of adjuvants by themselves or mixed with unadjuvanted vaccines, as being discussed now by CDC, makes the purchase some months ago of nearly $1/2 billion worth of squalene adjuvants make sense in the limited fashion that injecting a a known poison into large number of humans might be said to make sense.
Squalene, when injected into animals, causes such severe auto immune illness that its use is standard in laboratories where the induction of such disease is desired for research purposes. In that context, it is named after the scientist who discovered that it had that impact and is known as “Freund’s Adjuvant.
SKS: Trials in children began in mid-August, and trials in pregnant women have just begun.
REL:Does that mean that approval for the use of these vaccines for unrestricted use is based on …what? Certainly not science or data.
SKS: Our expectation is that vaccine will be a good match for the virus currently circulating in the United States based on intensive monitoring of the virus.
REL: But the expectation of the FDA and WHO for a “good match” between a circulating influenza virus and the next season’s disease is wrong well over 70% of the time. Secretray Sebelius, you and your Staff’s expectations are less than compelling. The regular administration of the seasonal flu vaccine that ACIP and CDC, both units of FDA, recommend year after year has been shown to increase the incidence of Alzheimer’s Disease by more than 600% while its accuracy in predictng which virus will be circulating is less than 30%.
FDA standards are not very high: according to your official website, the H1N1 vaccine will be considered a success if the anticipated antibody titer response (1:40) is found in 28% of the population. That means that these vaccines are being approved even if the number of people who do not show a robust laboratory antibody response (which is not associated with protection) is as high as 72%. So the risks of these vaccines are not accounted for and the efficacy is not required.
Furthermore, FDA has announced that the unadjuvanted vaccine, the strain change variety, is expected, under the best case scenario, to kill at least 30,000 people. The number who are expected to be maimed and crippled by this is not specified on the offical FDA website. If the 1976 disaster, which Secretary Sebelius says the FDA is looking to for guidance, is any indication, we can expect at least a thousand people sickened and crippled for each person who dies from the Vaccine. The math is hardly conducive to confidence in the FDA.
SKS: We are coordinating this 2009 H1N1 vaccination campaign with the seasonal influenza vaccination campaign, and are working hard with state and local authorities and the clinical community to address the challenges this presents.
From what we know as of today, 2009 H1N1 virus preferentially affects a population different from that affected by seasonal flu. In particular, this virus is infecting more young people including children, younger adults and pregnant women.
REL: What is this data based upon, given the lack of diagnostic specificity and the fact that symptoms are not distinguishable from all other types of colds or flus?
SKS: Typically these groups, particularly young children and pregnant women, are at greater risk of serious complications from any influenza, including the 2009 H1N1.
REL: Again I must ask, Secretary Sebelius, without diagnosis, how can that be ascertainined?
SKS: CDC’s Advisory Committee on Immunization Practices (ACIP) recommended on July 29 providing initial doses of the new H1N1 vaccine to five groups—approximately 159 million people.
REL: That is over one half of the entire population of the US. Wouldn’t it be more prudent, given that there is no legitimate health emergency, to not vaccinate more than half of the country, specifically the most vulnerable half, with an untested, unnecessary and uninsurable group of vaccines?
SKS: CDC endorsed these recommendations.
REL: Rather than reassuring me, this seems to me to be a clear cause for an overhaul of FDA and CDC with the possibility of criminal charges being investigated.
SKS: These groups are:
people who live with or care for children younger than 6 months of age,
health care and emergency services personnel,
persons between the ages of 6 months through 24 years of age, and
people from ages 25 through 64 years who are at higher risk for novel H1N1.
REL: Note your use of the term “Novel”, Secretary Sebelius. As stated above, that precludes the claim that these vaccines are mere strain change variations on a well-worn theme.
SKS: because of chronic health disorders like asthma and diabetes or compromised immune systems.
REL: These are the very groups to whom squalene is the most dangerous and the crops to whom contaminates like leukemia-causing virus SV40, found in the line of monkey kidney cells that the Novartis Vaccine has been cultured.
SKS: The H1N1 virus is particularly dangerous to healthy women who are pregnant. Not only has this virus caused greater numbers of pregnant women to be hospitalized, it has also been fatal in a higher percentage of this population than in other affected groups.
REL: Does squalene cross the placenta. Does it damage the fetus? In what way? At what age? It is known that mercury does cross the placenta and does damage the Fetus. Yet the CDC is advising women to take the H1N1 vaccine(s) regardless of whether it has the preservative known as “Thimerisol” (49.6% mercury by weight). No mention has been made of the dangers of aluminum adjuvants, nor of the fact that polysorbate 80 (also called “Tween 80) is associated with infertility when injected?
SKS: The federal government will be working in partnership with states, territories, tribes, and local communities as well as the private sector to help distribute and administer the new H1N1 vaccine. Thanks to support from Congress, the federal government has allocated $1.444 billion for states and hospitals to support planning and preparation efforts. TARP AGAIN.
The large scale 2009 H1N1 vaccine program will begin mid-October with small amounts of vaccine becoming available the first full week in October. The vaccine itself will be available free of charge to the American people, but some public and private providers may charge an administration fee. It will be distributed to providers and state health departments in a manner similar to how federally purchased vaccines are distributed in the Vaccines For Children program. The CDC and states will work with a contractor to get vaccine to where it needs to go. The number of doses shipped will be reported to the CDC daily, and the number of doses administered will be reported to the CDC weekly.
REL: Where will the adverse relations be reported for the general public to track?
SKS: The fact that vaccine won’t begin distribution until October makes preventing the spread of flu even more critical. Again, we need to remind all Americans about the things they should be doing right now: washing hands, staying home if you’re sick, and taking the necessary precautions to stay healthy and avoid getting sick. Flu.gov has good tips for what you need to do to avoid getting the flu.
While the 2009 H1N1 flu virus has been the focus of attention since the spring, it is important that we do not forget the risks posed by the seasonal flu viruses. More than 36,000 people die each year from complications associated with the flu.
REL:This statistic is totally false and misleading. About 600 people per year from the complications of influenza, but marketing concerns have created this oft-repeated number from which bears little relationship to reality as the swine flu case numbers or death numbers.
SKS: CDC continues to recommend vaccination against seasonal influenza viruses, especially for all infants, children, and people at greater risk for influenza complications. Seasonal flu vaccine already is becoming available in many places.
It is not too early to get a seasonal flu shot as soon as it is available. The protection you get from the vaccine will not wear off before the flu season is over.
REL: There is no evidence that the seasonal flu strain in the vaccines is the one circulating but there is considerable evidence that the vaccines are dangerous, despite insistent government and industry denial.
SKS: Closing Remarks – At HHS, we are simultaneously working hard to understand and control this outbreak…
REL: What outbreak? See above.
SKS: …while also keeping the public and the Congress fully informed about the situation and our response. We are working in close collaboration with our federal partners as well as with other organizations with unique expertise that helps us provide guidance for multiple sectors of our economy and society. It is important to recognize that there have been enormous efforts in the United States and abroad to prepare for this kind of an outbreak and a pandemic.
REL: One would have to wonder why.
SKS: Our nation’s current preparedness is a direct result of the investments and support of the Congress and the hard work of state and local officials across the country. While we must remain vigilant throughout this and subsequent outbreaks, it is important to note that at no time in our nation’s history have we been more prepared to face this kind of challenge.
REL: Or more over-prepared to face a challenge which does exist.
SKS: But the government cannot solve this alone and, as I have noted, all of us must take constructive steps. Taking all of those reasonable measures will help us mitigate how many people actually get sick in our country.
We look forward to working closely with the Congress to best address the situation as it evolves in the weeks and months ahead. Again, Mr. Chairman, thank you for the opportunity to participate in this conversation with you and your colleagues. I look forward to taking your questions.
REL: Thank you Madam Secretary. I do think you have told us quite enough disinformation.
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Today there was a treat and a terror in my email box: a new article from William Engdahl. A treat, because William Engdahl is one of my heroes. I do not know whether to admire him most as a writer who researches or a researcher who writes. Looked at either way, however, he is an honest and fearless man whose works tell us what we need to know – and what the self-anointed elite does not want us to know. And they do so with passion, clarity but without the faintest hint of panic or hysteria.
A terror because of the subject: mercury and aluminum in our babies and our own bodies through the mechanism of vaccination. You have heard it before: mercury and aluminum are neurotoxins. The restatement of this information in the context of a clear and focused historical and scientific review of just what we are talking about when we talk about mercury, aluminum and autism. It must be read and shared.
There are a few more facts which help to frame the cataclysmic disaster called “Vaccine Injury”, which is by no means limited to children. Think for a moment of healthy young men and women in coma, developing demyelinating neurological disorders like MS, ALS (now seen in children and adolescents for the first time in history as a new disease called “Juvenile ALS, but only in girls and women who have received Gardasil), diabetes, encephalitis, meningitis, persistent and debilitating rashes, swollen, painful joints everywhere in the body, brain fog, memory loss, depression, loss of IQ, lupus and other auto immune disorders, Alzheimer’s Disease, etc.
They Would Have Died Anyway
Let’s start with the origins of Thimerisol, which is 49.6% mercury by weight. Mercury is more toxic by far to tissues, including the brain, than lead.
It was patented by Eli Lilly, a so called “ethical” drug company (so named because they sell patented medicines) in the 1920s. In 1930, it was administered IV to 22 meningococcal meningitis patients, all of whom were in coma. All 22 patients died.
Eli Lilly, an “ethical” drug company, concluded that Thimerisol was safe because although all patients died, none showed any adverse response to the injected Thimerisol since they WOULD HAVE DIED FROM OTHER CAUSES ANYWAY. Therefore, none died from Thimerisol and it was deemed to be safe. When the FDA was founded, this information was presented to it and accepted. Thimerisol was grandfathered into use. The FDA, always compliant to the desires of industry, bought the insane logic of the “ethical” drug company, to the endless tragedy of our children, our elders and ourselves. This horrific substance is added to our vaccines as a “preservative”.
As a simple side thought, if vaccine manufacturing were strictly clean and sterile, not careless, contaminated and dirty, why would a preservative be necessary? Thimerosal was subsequently introduced for use in vaccines and in over the counter remedies as a preservative to kill bacteria in the product without any additional safety testing of any kind since it had been “grandfathered”. The 1930 study, in which every patient died, remains the only safety testing done on the substance even after being in use for over 84 years.
Aluminum is added to vaccines in order to irritate the immune system and increase the production of antibodies which are ASSUMED to be associated with immune competence with respect to the disease entity on which the vaccine is focused. No compelling (or even non-compelling) scientific evidence exists which demonstrates that this type of antibody production is associated with protection from the disease. In fact, virtually every epidemic in modern times has occurred in fully vaccinated populations.
Aluminum is neurotoxic and is strongly associated with the epidemic of a previously unknown type of dementia which will impact more than half of those who reach the age of 80: Alzheimer’s Disease.
When combined with fluoride, also added to many vaccines, the two toxic metals are strongly synergistic, increasing the neurotoxicity of the other substance by many times, creating a much higher level of impact than either one alone could produce. Since nearly everyone in the US drinks fluoridated water and brushes their teeth with fluoride-containing toothpaste, even without added injected fluoride, the synergistic potential is both untested and very frightening.
These metals are not the only toxins found in vaccines, but they are, individually and in combination, enough to create the public health and private home tragedies which can be laid directly at the feet of Big Pharma and criminal regulators.
Please disseminate this blog as widely as possible with full attribution AND with the Action Items above: they are vital to our ability to stay unvaccinated, all of us, with the new and much deadlier Swine Flu vaccines. Safety testing, if you can call it that, will not be completed until July of 2010. Yet the WHO and FDA (CDC is part of FDA) are rushing to vaccinate our precious children, pregnant women and the chronically ill with a vaccine containing aluminum, mercury AND a million times more squalene than the wildly toxic anthrax Vaccine A which caused the horrific, and frequently lethal, Gulf War Syndrome in hundreds of thousands of Gulf War vets and is still causing the same damage in our soldiers now.
Despite that, the Department of Defense, Governor after Governor and employer after employer are making these untested vaccines mandatory even while the President and Secretary Sebelius of Health and Human Services intone solemnly that vaccinations will be “voluntary”, defining “voluntary” as one option of a pair of options which offer you the unsafe, untested, unnecessary and uninsurable vaccine, all liability for which both the government and the manufacturers have been relieve of in a convenient legislative and regulatory pirouette. The other option is involuntary internment or incarceration, as the public documents from Iowa, Florida, North Carolina and other states makes clear is already being prepared for you. Indeed, “vaccine refusers” in Massachusetts may, under a pending law, be liable to fines of $1000 per day for refusing to be vaccinated AND jailed for up to 30 days [Per day of refusal? For all days of refusal? – REL]
So, indeed, “it IS the Vaccines, Stupid!” as William Engdahl tells the FDA, the media and the rest of the deaf establishment.
F. William Engdahl
September 6, 2009
Part I: Evidence Linking Autism Rise in Children to Vaccinations
The WHO and US Government CDC are escalating a public psychological
conditioning to create hysteria and panic among an uninformed public about an
alleged “virus” H1N1 Influenza A, aka Swine Flu, whose alleged effects to
date appear comparable with a common cold. Before people line up in the
streets demanding their vaccinations for their children and themselves, it
would be wise to remember, to paraphrase a 1992 campaign statement of Bill
Clinton to George H.W. Bush: “It’s the vaccination, Stupid!”
By countless scientific accounts, far more dangerous to human health than any
reported incidences of Swine Flu are the dangers of severe health issues
including paralysis, brain damage and even death arising from what is added to
vaccines by virtually every major vaccine maker. Almost without exception, all
commercial vaccines today contain various substances known as adjuvants
designed to make the vaccine “work.” These adjuvants are the source of
horrendous and sometimes deadly damage.
It has been speculated for some time that there might be a link in the
alarming rise in cases of autism among tiny infants and children and massive
multiple vaccinations today given routinely to infants and children from the
first hours of birth. There is clear and
shocking evidence of the link between the two. If you do not have a strong
constitution, you are advised not to read further.
A new study shows a direct link between standard childhood vaccination series,
MMR, and autism-like symptoms in monkeys. The principal scientist involved in
the study, Dr. Laura Hewitson of the University of Pittsburgh, presented the
alarming conclusions as an abstract pending publication at the International
Meeting for Autism Research. It has been presented at scientific conferences
in both London and Seattle, USA.
The study compared vaccinated macaque monkeys with non-vaccinated macaques. No
major flaws in the study have been revealed by any attending scientist. The
vaccines included the popular MMR series. The study found a marked increase in
“gastrointestinal tissue gene expression” and “inflammation issues”
with those monkeys which received vaccinations. They are a common symptom of
children with regressive autism.
The study also found marked behavior changes and development differences in
those monkeys given the vaccines versus those who were not. “Compared with
unexposed animals, significant neuro-developmental deficits were evident for
exposed animals in survival reflexes, tests of color discrimination and
reversal, and learning sets,” the study`s authors reported. “Differences
in behaviors were observed between exposed and unexposed animals and within
the exposed group before and after MMR vaccination.”
US Government-mandated research approved by Congress was t
o begin this year, but the funds were rescinded in early January. Claiming
“conflict of interest” because of ongoing court cases, the Centers for
Disease Control and Prevention (CDC), a long-time supporter of infant
vaccinations, withdrew the research plans.
The most shocking of all is the recent and now common medical practice,
reinforced by an aggressive pharmaceutical industry, of giving multiple
vaccines, often virtually within hours of birth, to infants despite the fact
that no study including all of the vaccine series commonly given to children
in the US and UK, about 30 in all, has been conducted until now. The practice
of newborn multiple vaccinations has become widespread in Germany and other EU countries over the past decade. Significantly there have surfaced reports of dramatically increased instances of autism in newborn and infants in various German hospitals over the past decade, precisely the period multiple
vaccinations of newborn and infants has become routine.
US Government coverup
Tragically, the US Government agency theoretically entrusted with guarding
public health, the Food and Drug Administration (FDA), as with the case of
health dangers of GMO foods, as well with the dramatic evidence of the link
between autism and adjuvants used in typical vaccines, is accepting the
argument of big and politically powerful Pharmaceutical companies.
The Food and Drug Administration considers vaccines safe but, just as with
GMO, they have done no studies into the effects of multiple vaccinations as given in the common childhood series which started in the 1990s in
the USA and spread to the UK and now across the EU.
According to Robert F. Kennedy, Jr., son of the late Attorney General and an
attorney active in campaigning to expose mercury (Thimerosal) and other
toxicity dangers in vaccines, recently stated, “as autism is a behavioral
affliction rather than a precisely defined biological injury —
epidemiological studies are critical to establishing its causation. But the
greatest source of epidemiological data is the Vaccine Safety Datalink (VSD)
— the government maintained medical records of hundreds of thousands of
vaccinated children — which Health and Human Services Department has gone to great lengths to keep out of the hands of plaintiffs’ attorneys and
independent scientists…The raw data collected in the VSD would undoubtedly
provide the epidemiological evidence needed to understand the relationship
between vaccines and autism. The absence of such studies makes it easy for
judges to say to plaintiffs they have not met
their burden of proving causation.”
Autism was virtually unknown in the United States until 1943 when it was
diagnosed and identified eleven months after Thimerosal, a mercury-based
vaccine “adjuvant” was first added to baby vaccines along with various
aluminum compounds in the United States. Thimerosal is often used to stem
fungi and bacterial growth in vaccines despite massive evidence of its severe
effects as a potent neurotoxin. Following independent studies, Russia, Japan, Austria, Denmark, Sweden and Britain have banned Thimerisol from children’s vaccines. Germany to date has no such ban. The toxin was developed in 1930 by Eli Lilly. Tragically in 1991, despite overwhelming evidence to the contrary the US Government’s Center for Disease Control (CDC), the same agency fueling the current hysteria over the non-proven H1N1 Swine Flu virus danger, recommended that infants be injected with a series of mercury-containing vaccines in some cases within 24 hours of birth for Hepatitis B and two months for diphtheria-tetanus- pertussis.
Before 1989 US pre-school children received eleven vaccinations— polio,
diphtheria-tetanus- pertussis, measles-mumps- rubella (MMR). By 1999, because of the various CDC recommendations, the number of vaccinations was twenty two before first grade of school. Parallel with this explosive rise in
vaccinations of the very young in the United States, according to Kennedy, the
rate of autism among children. The state of Iowa reported a 700% increase in
autism in children beginning in the 1990’s and along with California has
banned mercury in vaccines. Despite evidence, however the US FDA continues to allow drug makers to include Thimerosal in numerous over-the-counter
non-prescription medications as well as steroids and injected collagen. The US
Government ships vaccines preserved with Thimerosal to numerous developing
countries as well, where some are reporting sudden explosion of autism rates
as well. In China,20where autism was unknown before introduction of Thimerosal by US drug makers in 1999, press reports indicate there are almost two million autistic children.
Instances of autism in the US exploded as some 40 million children were
injected during the 1990’s with Thimerisol-based vaccines, giving them
unprecedented accumulations of mercury poison. The level of ethylmercury in a
vaccine routinely given then to children of two months age was 99 times
greater than the US Government’s daily limit for exposure. As with the
current WHO pandemic declaration around H1N1 Swine Flu, the CDC Vaccine
Advisory Committee is filled with scientists with close ties to the
pharmaceutical industry. Dr. Sam Katz, chairman of the committee was a paid consultant to most companies producing the vaccines he “recommended.”
The aluminum danger remains
While vaccines available in the US today exist with no Thimerosal (50%
mercury), virtually all vaccines still contain aluminum, which has been linked
to impaired neurological development in children. Aluminum has not replaced
thimerosal as a vaccine preservative; it has always been used in vaccines.
In the recent past, most US children got exposed to both thimerosal and
aluminum simultaneously with the hepatitis B, Hib, DTaP (diphtheria, tetanus
and pertussis) and pneumococcal vaccines. Combining mercury with aluminum
increases the likelihood that the mercury will damage human tissue.
According to a recent report by Michael Wagnitz, an American chemist, “Currently eight childhood vaccines that contain aluminum ranging from 125 to 850micrograms (mcg). These vaccines are administered 17 times in the first 18months of life, an almost six-fold increase compared to the vaccine schedule
of the 1980s.”
Wagnitz adds, “According to the American Society for Parenteral and Enteral
Nutrition, based on IV feeding solutions, a child should not exceed a maximum
daily dose of 5 mcg of aluminum per kilogram of weight per day. That means if
a child weighs 11 pounds, the child should not exceed 25 mcg in a day. This
level was determined to be the maximum safety limit based on a study publishedin the New England Journal of Medicine titled “Aluminum Neurotoxicity in Preterm Infants Receiving Intravenous Feeding Solutions.”
The hepatitis B vaccine, administered at birth, contains 250 mcg.
In a 1996 policy statement, “Aluminum Toxicity in Infants and Children,”
the American Academy of Pediatrics states, “Aluminum can cause neurological
harm. People with kidney disease who build up bloodstream levels of aluminum
greater than 100 mcg per liter are at risk of toxicity. The toxic threshold of
aluminum in the bloodstream may be lower than 100 mcg per liter.” What level
of aluminium toxicity is contained in vaccines routinely given German, French
and other children n the EU is not known. It might be time for a public demand
for such information to be disclosed, and before governments launch mass
vaccination campaigns for untested vaccines against a non-proven H1N1 Swine Flu threat.
At last! An effective and powerful legal action with the potential to stop the FDA’s planned approval of Swine Flu Vaccines without any, repeat ANY, safety testing. Three far sighted health freedom leaders have banded together to take action to protect us all and invite your help, and your organization’s help, too.
We, you and the Natural Solutions Foundation, ARE the net roots of health freedom. We can – and do! – produce literally millions of emails, raising our voices high enough to push back the madness. In fact, we’ve already sent more than 1.5 million emails demanding the right to say “No!” to pandemic vaccines. Well, it is time for more of same!
If you have not yet clicked on the Action Item demanding the right to say NO! to the vaccine without then going to jail, now is the right time to do so for every member of your family:
Silly Season Science is the product of shameless intellectual prostitution in which science for hire pumps out whatever it is told to produce. A prime example from the supposedly reputable British paper, The Guardian:
“Healthy Eating Can be Sign of Serious Psychological Disorder”
Health Freedom Silly Season has to end, now. You see, Health Freedom organizations are notorious for NOT working together. You know, this one says this, and the other one says that and pretty soon you don’t care “who struck John” and you are sick of all the gore! That’s one of the classic disinformation techniques and juvenile people are easily stimulated to behave like tantrum-ing toddlers. You have noticed that the Natural Solutions Foundation does not waste its time, or yours, with that kind of sniping and in-fighting. Instead, we focus on the problems, find solutions and tell you what we think is going on, asking for your help.
But when the folks that like to call themselves part of the Health Freedom movement behave that way, it means they are notoriously shooting themselves in the foot. Since they are supposed to be working for you, that also means they are not doing their job protecting your interests. If they had been, perhaps we would not be in this mess and perhaps General Bert and I would still be running our drug-free practice of medicine.
This issue, mandatory/unapproved vaccination, is really the ultimate litmus test: either the other “Health Freedom” organizations actually get on board and join us in protecting your rights to stop this dangerous – possibly lethal – FDA idiocy or they are, in fact, NOT health freedom anythings.
High Road To Survival
You see, once again, as we continue to do, the Natural Solutions Foundation is offering the hand of literally life-saving collaboration to any and all other health freedom organizations and advocates. Those who join us are welcome, no matter how inappropriate or inflammatory their previous bad behavior and disinformation activities have been. This is literally a matter of YOUR life and death.
Those who do not join us are making who they are, and who they work for, clear by marginalizing themselves.
Please contact the health freedom organizations of your choice to urge them in the strongest terms to get on board with this powerful initiative. If they resist, ask them to explain, in writing, why they are not taking this opportunity to work for your health and freedom, and that of the other supporters/members of the group. Insist on real reasons for their inaction, not merely unsupported assertions and, if they cannot provide them, walk away. They are not on your side. They just proved it.
On the other hand, smart non-governmental organizations are happy to cooperate to make sure Health Freedom can survive. For example, we’ve just accepted DownSize DCs invitation to join its coalition partners in www.ConsumerCenteredHealthcare.org to “Stop current efforts to expand government control of health care – Roll back existing government involvement and restore free market competition” No matter what healthcare system exists, we want it to a system that allows people the freedom to make their own choices… and a politician and bureaucrat dominated system cannot do that! Whoever pays for it, your health care choices should be, must be, determined solely by you.
Three leading health freedom advocate organizations banded together this week and, under the guidance of Ralph Fucetola, JD, Natural Solutions Foundation’s brilliant and skillful Counsel and Trustee, submitted a Citizens Petition (unlike an Internet Petition, a Citizens Petition is a powerful legal challenge which can have real impact on Policy) to the FDA demanding redress from the immanent harm posed by approval of attenuated and adjuvanted live virus vaccines for a trivial disease when not one of the vaccines have been tested for safety. You will recall that on July 23, 2009 the Fraud and Death Administration said that they will approve these vaccines in the absence of completed safety tests.
Remember, the pediatric tests of the vaccine now underway are to determine antibody response levels (dosage), NOT safety. And the vaccines being tested are NOT those with adjuvants.
The Health Freedom movement has been divided by disinformation and ego-based squabbles for decades. Enough. The issues are too important to let absurd accusations and personal turf struggles interfere any longer.
Health advocates, officials and doctors, along with and health freedom leaders, have all known for quite some time that the enormously profitable Swine Flu Vaccines are a vast windfall for Big Pharma and a horrific dangers for the rest of us.
The New York State Association of Nurses refused New York State’s Mandatory Vaccination regulation for mandatory health care worker vaccination without any provision for exemptions of any kind.
In the UK, where the Daily Mail leaked two letters from their Health Protection Agency and a leading neurologist urging other neurologists to be on the lookout for an anticipated 800% rise in the incidence of Guillian Barre Syndrome, also known as Polio, following the upcoming MANDATORY Swine Flu vaccinations there. http://dailyexpress.co.uk/posts/view/120936/Alert-on-killer-side-effect-of-the-swine-flu-vaccine-/, nurses are so uneasy about the mandatory Swine Flu vaccine’s dangers, and the non-seriousness of the “Pandemic” disease, that 2/3 say they will either refuse the Swine Flu vaccine outright or are unsure that they will submit to it. In fact, only 1 nurse in 7 receives the seasonal flu vaccine in the UK anyway. Skepticism runs high among people in the know!
for a look at the good, the bad and the just plain meaningless.
The Citizens Petition which we have filed with the FDA is, we believe, a highly effective way to exhaust our legal remedies so that we can rapidly and effectively move forward. We need your help, though. Your organizations and you (and your family, friends, contacts, etc.) all are invited to join the Petition and exercise your First Amendment Right for redress of grievances via a Petition to the Government.
All 6 Swine Flu vaccines which the FDA has announced it will approve BEFORE the completion of any safety testing are unsafe. Some or all will have squalene-based adjuvants. Some or all will have live attenuated virus (LAIV) vaccines which have been shown to
* Increase hospitalizations of children for all causes by 300%
* Cause wheezing and asthma,
* Communicate the vaccine disease to those with health problems and weak immune systems
* Add new bits of other viruses in the warm, wet, nutrient rich environment of a cell
* They provide little or any real or lasting immunity against the target disease.
Oil in water adjuvants such as sqalene or its related compounds have never been approved for injection in the US and, in fact, have been rejected by the FDA itself because they were “too dangerous to test in the United States”. Tragically, they were used against our own military creating the cataclysmic auto immune disorder known as “Gulf War Syndrome”.
Health Without Freedom?
Let’s make an incorrect assumption for a moment, just for the sake of argument. let’s assume that untested LAIV vaccines with deadly adjuvants were safe and effective. Even if they worked and were safe, is it OK with you to force your kids and you, too, to be vaccinated at someone else’s choice? I think not and I am quite certain that you think not, too.
Health freedom IS our first freedom and making this type of decision for ourselves IS the hall mark of freedom. Take each of these Action Steps once for each member of your family, then alert all your contact to do the same to help keep health freedom free – and help keep yourself alive!
I will bet that you thought that the Constitution of These United States gave you the right to a fair trial along with life, liberty and the pursuit of happiness, didn’t you? And you thought that innocence was a defense before the bar, didn’t you.
Well, Supreme Court Justice Antonin Scalia thinks differently – very differently. Justice Scalia recently wrote that that there is nothing inherently un-constitutional about executing an innocent person.
In his dissenting opinion in the appeal of convicted – but innocent – felon Troy Anthony Davis, Justice Antonin Scalia took his Supreme Court colleagues to task for thinking that mere innocence is grounds to overturn a conviction: “This Court has never held that the Constitution forbids the execution of a convicted defendant who has had a full and fair trial but is later able to convince a habeas court that he is “actually” innocent. Quite to the contrary, we have repeatedly left that question unresolved, while expressing considerable doubt that any claim based on alleged “actual innocence” is constitutionally cognizable.”
You do not have to be a lawyer to understand that the very atoms of the molecules of the thread of the fabric of the Constitution of These United States are being destroyed from within the so-called “Justice System”. If you think that your right to protect your body from dangerous pharmaceutical interventions will be protected by the Justice System as it is now, in light of this madness, think again.
With a Supreme Court of this type, we clearly want to impact the regulations BEFORE we ever get to the point of needing the Court’s help! To protect us all from the vaccines, we need to grab the legal system, which means, in this case, the FDA, by its metaphoric parts, and force it to protect us while we have access to it and can still control some of its actions. And for that, we need your help, in force. NOW!
Speaking of Rights, Does the US Have As Much Freedom of Speech as India? Apparently Not!
In the US, we like to think that our Constitutional system assures us of freedom of speech that we can rely upon, more than any other country.
In fact, however, the FDA imposes a profoundly un-American gag rule on what you can or cannot say – or learn – about the health benefits of food and food components and will put manufactures out of business if they tell you the truth about health freedom with legal methods or with their ax-wielding, gun-toting, dog-using goons called FDA Marshals.
Take Swine Flu (NOT the Swine Flu vaccine, of course – don’t take that!): The FDA has criminalized the discussion of ALL options to prevent, treat, mitigate or cure Swine flu except Swine Flu Vaccines and the [quite dangerous] anti viral drugs Tamiflu and Relenza.
But my friend in India, the noted Dr. Leo Rebello, notes that although doctors at Kasturba Hospital of Infectious Diseases in Mumbai (formerly Bombay) maintain, falsely, that they don’t know why a baby born to a mother who supposedly had Swine Flu [although tests for Swine Flu are wrong 90% of the time, so how could they tell?- REL], they do, in fact, know why the baby died: it died because its mother was given Tamiflu!
He states, “The adverse or side-effects of Tamiflu are – delirium, hallucination, delusion, disturbances in consciousness, abnormal behavior and convulsions. Allergic reaction including severe rash, nausea, dizziness are the common reactions. Children under 12 months and pregnant and nursing mothers and those who are allergic to oseltamivir phosphate – the main ingredient – or any other ingredients in Tamiflu should not be given Tamiflu. H1N1 is a bio-weapon and Tamiflu in combination is designed to control the population. We will have on hand another tragedy like Thalidomide if Tamiflu is given so recklessly.”
Dr. Rebello goes on, in what the FDA has previously announced would be criminal speech if, for example, I were to tell you this information,
“There are much better, safer and cheaper Flu medicines in Ayurveda and Homeopathy. Amla which contains the highest level of Vitamin C as also Mosambi (sweet lime) and Santra (orange) and simple Nimbu Pani bring immediate relief in Flu.
In Homeopathy, as I have already written :
We have Arsenic Album 200 — cold, running nose, cough and feverishness.
Bryonia Alba 200 — cold, cough, fever, headache, giddiness.”
If I were to tell you in the USA, as I could in India, that Nano silver, www.Nutronix.com/naturalsolutions, is outstandingly effective in killing this virus (and all others against which it has been tested) and then point you to an article by Gordon Peterson, PH D, which states,
Antibiotic drugs provide no solution against the virus but can be very beneficial for pneumonia that develops later. A broad spectrum antibiotic should be used because there are numerous bacteria that can produce pneumonia. According to a Penn State publication, silver sol can be given with the antibiotics and produce up to a tenfold increase in antibiotic activity.
There are hundreds of supplements that can be of significant benefit for the immune system and even some that claim to have antiviral activity. The best proven choices for nutritional supplements come in the form of immune stimulants and wellness products. These include: immunity Vit C, B complex, folic acid, vit D (prevention) ginseng, Echinacea, garlic, probiotics, expectorants and silver sol.
CDC recommends one in every room. HEPA air filters use silver to inactivate viruses and can effectively kill 99% of all bacteria, and viruses in minutes.
Proper hygiene and a water purifier are recommended by the CDC because the influenza virus can survive 100 hours in water. Get one that has a silver filter that can actually destroy the virus. Carbon, filtration, reverse osmosis does not destroy or remove the virus.
Topical disinfectants are recommended by the CDC for use between each patient and can kill germs for 4-6 hours. Patients and health care professionals should use these 4 times a day or as needed. Silver so gel demonstrates effectiveness against some of the worst pathogens including: MRSA, VRE, Strep, and the other bacteria that cause pneumonia.
Prescription drugs and vaccines “treat” and [may -REL] help prevent viral infection and disease but are not capable of totally controlling a dangerous new or novel virus. Nutritional supplements such as Vitamins, Minerals, Echinacea, Ginseng, Probiotics and many others have the ability to help boost immune function and improve natural defenses which results in some defense against disease causing viruses and the associated secondary infections
Silver Sol provides proven prevention and treatment against viral and bacterial infections, while there is nothing else with such broad spectrum benefits. In addition, Silver Sol can be safely taken every day for prevention where it has been shown to provide protection against the very dangerous Bird flu H5N1.
The combination of antibiotics with Silver Sol has been shown to enhance antibiotic function by as much as ten fold due to the fact that Silver Sol kills the residual pathogens that the antibiotics cannot. Results of the combination of 19 different prescription antibiotics and silver sol demonstrate safe additive and/or synergistic benefits across 7 different pathogenic strains (Staphylococcus, MRSA, E coli, Pseudomonas arugenosa, Salmonella and Streptococcus). The results of this combination therapy result in significant pathogenic destruction while helping to reduce bacterial resistance (19). This can be attributed to the fact that Silver Sol does not produce resistance, nor does it destroy the beneficial intestinal probiotic bacteria.
…It is evident that the newly patented EPA certified and FDA approved Silver Sol technology provides tremendous treatment options for prevention and combination therapies. Silver Sol gel can help stop viral spread on the most contagious areas like hands, nose, mouth and skin. It is sufficiently documented and proven to be considered to be a first line of defense against Influenza and a significant companion to antiviral and antibacterial drug regimens topically and orally.”
Swine Flu Influenza Type A/H1N1 Protection for Health Care Practitioners and Their Patients, http://www.worldhealth.net/news/swine_flu_influenza_type_a_h1n1_protecti4
If I said that, I would be violating the FDA’s regulations which, in the US, have the strength of law.
Happily, we’ve got Rep. Ron Paul, MD (Tx-R) on our side. He has introduced two bills to end this unconstitutional rule by edict by the Fraud and Death Administration (FDA) and the Fake Trade Commission (FTC).
We urge you to join the dozens of thousands of people who have already told their members of Congress that they co sponsor and support HR 3394 and HR 3395.
Health freedom, your freedom, is facing enormous challenges right now. I cannot remember them coming so fast, or so furious. And the Natural Solutions Foundation is working on the most important ones of all:
for background information and talking points leaflets.
2. Free Health Speech being gagged
3. State and Federal mandated Swine Flu
You can imagine that keeping up with health freedom is an enormous job which requires diverse skills and talents. You can also imagine that we need hands, but not just any hands: hands that are connected minds, hearts and brains.
That is why we are asking for volunteers for the Natural Solutions Foundation and, at the same time, volunteers for our Valley of the Moon Eco Demonstration Project, www.NaturalSolutionsFoundation.org, in Volcan, Panama.
We have building projects, marketing and development ones, administrative, communication, and a host of other needs. If you are interested in either an Expense Paid Volunteer Position (Room and Board in Volcan, Panama) or in joining the roll of Health Freedom Volunteer Sponsors, please join the Forum and contact Ralph Fucetola at ralph.fucetola “at” usa.net or me at dr.laibow “at” gmail.com with “Volunteer” as the subject.
to set up your recurring, tax deductible donation now.
Please visit our donations page and help us in any way you can; of course, recurring donations are the most important, since that allows us to plan ahead and be prepared for the Health Freedom battles to come!
Mark Your Calendar!
The Truth About Natural Cancer Cures
Date: Wednesday, September 2nd at 8:00 PM ET
Time: 8:00 PM ET
Instructor: Dr. Leonard Coldwell
Tuition: No Cost
Dr. Leonard Coldwell, Board Certified NMD DNM PHD LCHC CNHP DIP.PHC is the leading authority for cancer and stress related illness and has the highest cure rate for terminal diseases in Europe. Dr. Coldwell is the most endorsed holistic doctor in America and 11 times bestselling author. His newest book, Instinct Based Medicine, www.instinctbasedmedicine.com, has just been released and is already in the second Edition. Dr. Coldwell’s most awaited book: The Only Answer to Cancer, will be available in September 09.
Don’t miss this chance to spend time with this renowned physician and activist.
One of the largest vaccine trials ever has been announced by St. Louis University. That trial will enroll 167 people.
You read that right. One of the largest vaccine trials ever will involve fewer than 170 people. If you thought that vaccines were tested over the long term and on lots of people, thing again.
Not only that, the trial appears to me as if it is an attempt to find a use for out of date, or useless old flu vaccines.
Flu vaccines are pretty much useless anyway, from where I sit, but they are valuable, at least from the point of their makers and the people who have purchased them so any use they can be put to would be welcome to those who own them.
In an article dated September 8, 2008, St. Louis University announced that it would be trying a novel approach to Pandemic Flu prevention: using an old flu vaccine approved in 2004 to prime [in other words, to irritate it-REL] in order to develop “protection” against another version of the Avian Flu when a shot for that (or a different) strain of the virus that causes Avain Flu is given.
If I did not know better, I would say that someone with a lot of money invested in ineffective, dangerous and outmoded vaccines was looking for a new use for them. You see, each year, the World Health Organization, the CDC and other organizations get together in the Spring of the year and literally guess, yes that is correct – GUESS – which strain of the so called “seasonal flu” is going to come around next fall and cause the disease we know as “the flu”.
How good are their guesses? Pretty bad. â€œStatisticians at CDC say that influenza is inherently unpredictable, that itâ€™s such a random event that thereâ€™s no way that you can predict future outcomes,â€ said Forrest Nelson, professor of economics at the University of Iowa, says. http://scienceline.org/2007/05/23/hsu_health_flu-prediction/
Science Daily, reporting on a study published in Pediatrics, the journal of the American Academy of Pediatrics, noted “Each year’s flu vaccine needs to be designed in advance, based on which strains of virus are anticipated to be prevalent in the coming year. Because the accuracy of that prediction varies, the effectiveness of the flu vaccine also varies from year to year.” http://www.sciencedaily.com/releases/2007/09/070904072851.htm. This suggests, but does not document the CDC’s dismal record of prediction accuracy.
That record is so dismal, in fact, that a recent study which examined whether Seniors who were “properly” vaccinated were protected by the flu shot noted, ” Researchers say that older people suffering chronic conditions, such as lung disease, heart disease, diabetes, have even higher flu risk despite vaccination. Scientists thought that flu vaccine provides with 20-30% protection against pneumonia, but this research suggests that the protection level is only from 5% to 10%….Effectiveness of flu vaccine is different each year, it depends on how successful virus strain predictions for a current year will be. Flu vaccine cuts infection rates from 40% to 60% in the best cases.” http://www.emaxhealth.com/90/23622.html
But whether they are effective or not, flu vaccines are costly to make. True, they are wildly profitable if used but, when the populace figures out that they are both unsafe, unnecessary and do not provide protection, they do not use the stocks up, creating an economic blow for the highly economically motivated pharmaceutical companies.
On August 18, 2008, the St. Louis Business Journal wrote about the “quiet crisis” created by lack of increases in NIH funding. “St. Louis Business Journal — Five straight years of flat funding from the National Institutes of Health (NIH) have Washington University and Saint Louis University scrambling to fill financial gaps with other funding sources to keep biomedical research projects going.
Officials at both universities said they increasingly are using internal funds and applying for grants from private foundations and pharmaceutical companies to make up for less NIH money….Besides nonprofits, another source to which researchers have turned is pharmaceutical companies, but that’s not ideal either
“Our work doesn’t really mesh with them,” said Dr. Randy Sprague, a professor of pharmacology and physiological science at Saint Louis University. ” http://www.biospace.com/news_story.aspx?NewsEntityId=107184
Apparently, however, their work meshes well enough to try to use old flu vaccines to pump up the effect of new ones (which may or may not be made from viral strains which may or may not be causing disease in a body near you.
But you never know. It might work. Or, then again, it might not.
Of course, the impact of experimental vaccines, or extra vaccinations (94% of all available flu vaccines still contain mercury and all of them contain several (or all of the following): bits of fetal and animal tissue, “stealth viruses” which can cause cancer and other potentially lethal diseases, aluminum hydroxide (associated with Alzheimer’s Disease and especially toxic in the presence of fluoride), alumino-fluoride complexes, Polysorbate 80 (known to cause sterility), MSG (a brain irritant), mercury, formaldehyde, mixtures of viruses and bacteria, sometimes dead or inactivated. None of the vaccines have been subjected to any long-term safety trials (longer than a few weeks). Most were only studied for a few days and then approved if nothing untoward was detected by the Medical Advisory Committees, many of whom had large share-holdings or other vested interests in the vaccine companies, as recently revealed in US Congressional hearings.” according to Mike Godfrey MBBS, FACAM, FACNEM. http://www.healthy.co.nz/healthy-developments-news-item-138.html
The race to vaccinate against everything anyone, adult or child, could possibly experience began when vaccine manufacturers decided to use the US Congress to build a bulwark against the tremendous losses they were incurring by having to compensate parents for the damages their vaccines were doing to children. “By the 1970s, the manufacturers were losing very costly court actions for vaccine-damaged infants. They successfully lobbied the US Congress by threatening to stop manufacture, and in 1986, Congress gave them immunity from prosecution. This unique legislation allowed a commercial organization total freedom to start developing vaccines for all childhood illnesses. It also resulted in a massive commercial drive to mandate vaccination for every child before entering school.” http://www.healthy.co.nz/healthy-developments-news-item-138.html
And, of course, once the child hood vaccination market had been secured, adults, especially healthy adults, were the next market.
Whether for use in children or adults, however, vaccines and their toxic components, have never, repeat, never, been tested for safety in combination. That means that their dangers are less than unknown. Since vaccine manufacturers are totally protected from product liability, at least in the US, there is no reason for a manufacturer to spend money making the vaccines safe or testing them to make sure that they are, at the very least, not harmful.
So it is not outside the realm of possibility that this “largest vaccine trial ever” is just another ploy to make more money from vaccine stocks. Whether or not that is the motivation behind this “largest vaccine trial ever”, there are so many distressing aspects to the trial it is hard to know where to begin. A good place might be not to take flu vaccines!
Pandemic Preparation: SLU Launches Avian Flu Study
NIH-Funded Study Examines Combining Stockpiled and New Vaccines
September 08, 2008
Pandemic Preparation: SLU Launches Avian Flu Study
NIH-Funded Study Examines Combining Stockpiled and New Vaccines
ST. LOUIS — Saint Louis University School of Medicine seeks volunteers for one of the largest avian flu clinical trials in the United States to test a new vaccine approach to prevent the disease.
The study will test whether an injection of an FDA-approved avian flu vaccine created in 2004 can “prime” the body’s immune system so a second shot of a different avian flu vaccine can protect against avian flu infection. The second vaccine is an investigational vaccine, which has not yet been given to people.
“This study will answer several scientific questions, but the most important one is whether you can prime with one strain of influenza vaccine and boost the body’s immune system with another,” said Robert Belshe, M.D., director of the Center for Vaccine Development at Saint Louis University School of Medicine.
Vaccines protect against influenza by triggering the body to produce antibodies against infection. The study will examine the vigor of the body’s antibody response and the safety of the vaccines.
Creating an effective vaccine for the avian flu is challenging. Like any other influenza bug, the avian flu virus — known as H5 — is constantly evolving. In addition, two doses of vaccine are likely to be needed to prevent avian flu infection, said Belshe, who is the study’s principal investigator.
Avian flu occurs in birds, and in rare instances has crossed the species barrier to infect people. As of June 2008, the World Health Organization reported 385 human cases of avian flu and 243 deaths in Asia, Europe and Africa. The virus has not yet changed so it can be spread easily between people.
Public health experts are concerned that the avian flu could become the next influenza pandemic — or outbreak of disease that sweeps around the globe, causing millions of deaths worldwide — because previous outbreaks have been started by bird viruses. Consequently researchers are focused on finding a vaccine to protect against avian flu.
“Although many years have passed since the last major pandemic, the serious threat of pandemic influenza remains,” Belshe said.
“So far there has been no substantial leap between the bird species and humans. However other pandemics have started when the organism jumps between species and we’re worried it will happen again. A few genetic changes can occur in the virus and it would become highly infectious to humans. We’re trying to prepare.”
Saint Louis University is the lead site of the research, which is sponsored by the National Institute of Allergy and Infectious Diseases (NIAID), part of the National Institutes of Health and will include up to five study sites. Of the 500 volunteers who are being recruited nationally, up to 167 people will be enrolled at SLU’s NIAID-funded Vaccine and Treatment Evaluation Unit (VTEU).
The study involves four to nine visits to the VTEU and overall the study lasts six to 12 months, depending upon the group to which a participant is randomly assigned.
Potential study volunteers must be healthy, between 18 and 49 years of age, not pregnant and not allergic to eggs.
Participants will receive two vaccines — one or two doses of the 2004 avian flu vaccine that currently is stockpiled; one or two doses of the investigational vaccine that matches a different strain of the avian flu; or both vaccines.
For more information about enrolling in the study, please call the Saint Louis University VTEU at (314) 977-6333 or email email@example.com.
Established in 1836, Saint Louis University School of Medicine has the distinction of awarding the first M.D. degree west of the Mississippi River. Saint Louis University School of Medicine is a pioneer in geriatric medicine, organ transplantation, chronic disease prevention, cardiovascular disease, neurosciences and vaccine research, among others. The School of Medicine trains physicians and biomedical scientists, conducts medical research, and provides health services on a local, national and international level.