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!
Want to support the Natural Solutions Foundation by drinking Health Freedom’s own coffee (or detoxing with it) and giving it to lucky personal and corporate recipients this Holiday season? Visit http://ValleyoftheMoonCoffee.org and Wake Up to Health Freedom (TM) with pure, clean coffee from our teaching farm in Panama’s Valley of the Moon Eco Demonstration Project, www.NaturalSolutionsFoundation.org. Want to volunteer at the Valley of the Moon? Glad to have you. Visit http://www.natsol.org.
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”
While we still have some time, I urge you to add your voice to the nearly 2 1/4 million emails which are flooding the boxes of legislators at the State and Federal levels, secretaries Sebelius of HHS and Napolitano of DHS and the White House. Our voices are loud, and becoming louder. There is not much time to make them heard. Please go to http://salsa.democracyinaction.org/o/568/campaign.jsp?campaign_KEY=27275 and take action once for every one of your household members, then alert everyone you can reach to do the same. The push back is softening the response of the other side and that is of enormous significance. We need to make the use of these deadly vaccines simply unthinkable. In Germany, the first of the vaccine recipients are beginning to sicken and die from the shot. In Canada, Native Americans have received body bags along with their Swine Flu kits.
There are strong, but as yet unconfirmed, reports that 5 US Navy ships are under quaratine after a 96% flu outbreak rate following vaccination IN APRIL, 2009. Note that the vaccinations for Swine Flu were said to occur 5 months before the “was enough| Swine Flu vaccine, it was ready to test, it had been manufactured and the causative organism was known. We do not yet have information on which vaccine was used, sickening and killing so many healthy young people. But we do know that wherever it is used, it is designed to create the very disease that is being hyped and sold to the world as a fear source, without a shred of solid reason.
Perhaps it was Novartis H1N1 vaccine which the FDA pulled off the market place for labeling inconsistencies in February, 2009. Not enough vaccine? Needs adjuvants to make it go around? Balderdash!
This week coming we will try to make their use illegal, as well. Since the 1964 Keffauver Bill makes it mandatory for the FDA to require that a drug or vaccine be both safe and effective before it can be approved (although we all know how very lax that is), no such testing, lax or otherwise, was carried out before the 4 vaccines approved on September 15, 2009 by Secretary Sebelius were licensed for release into the general public.
Be aware, too, that the nasal mist vaccine by Medimmune is designed to create the flu, leaving immunocompromised people, children, cancer chemotherapy and radiation patients, children and adults on asthma medication, people with eczema and any other type of immune suppression, and babies less than a year old, vulnerable to the disease which will be spread by the nasal mist vaccine. Be aware, too, that this same preparation is to be avoided by pregnant women and the people mentioned above, including young children. Hmmm. How do you do that? How do you vaccinate First Responders, health care workers and pregnant women and children and keep the virus that they are involuntarily shedding from the patients in the hospital and the babies whom this virus will sicken and kill? Clearly, you don’t. Clearly the game is to make very sure that this novel virus, classified as a “Bio weapon” by the US Government, behaves better than SARS, Avian Fly and perhaps the 1976 Swine Flu.
When we enter this case in Washington DC this week, we know that we will likely be facing enormous legal expenses. So far our lawyers have been wonderful about fees BUT we cannot expect that largess forever. An appeal in Federal Court is a huge undertaking. We need two donations from you on a recurring basis, large or small.
The first ends in the number 6 and is thus earmarked for legal funds. The second ends in any other number and will help support us as we move forward on this and both are urgently needed. Click here, http://drrimatruthreports.com/?page_id=189, to keep your health freedom team fighting for you.
Of course, you could also purchase our outstanding all natural coffee at www.ValleyoftheMooncoffee.org. It is produced as part of our teaching effort to help reclaim the production of food here at the Valley of the Moon Eco Demonstration Project in Panama. It is free of GMOs, pesticides, herbicides, fungicides, suicides and it tastes like … well, it tastes like freedom! It is Health Freedom’s own Coffee and every bag you buy not only helps us, but brings you an 80% tax deduction discount as a “Thank you!|
Now would be a great time to select www.ValleyoftheMoon.org coffee as your personal and corporate gift for the 2009 Holiday Season! Large orders? No problem! Contact Gail Coba at “Gail Coba”
Squalene: Be Afraid, Part I
The following article by Edda West was published in 2005. Given the horrific threat of squalene laced vaccines for a mythical danger concocted in a lab, it is all the more relevant now. Please take time to read and share this post and the one that follows it.
This outstanding article details the mechanism of action, and the enormous dangers, of vaccines which contain squalene in any of its forms. But bare in mind as you read this clear, and enormously important article below, that the adjuvanted vaccine approved by the US Government on September 15, 2009, in the total absence of even a shred of safety testing, will contain 1 million times more squalene than even the deadly Vaccine A.
You may have encountered the squalene story before: how injected squalene, even a few molecules of injected squalene, causes the body to attack itself on a rampage of auto immune destruction like an army gone mad and turned on its country. And that is, in fact, exactly what triggered this onslaught of destruction: the US Department of Defense decided to experiment on its citizens, healthy young men and women who had made the terrible mistake of trusting their country to take care of them while they were willing to give their lives to defend it.
Instead, they were betrayed with unsafe vaccines for (or against, it depends on whom you asked) anthrax. The tragedy was that this was no experimental surprise which was revealed for the first time when the vaccine’s terrible consequences showed up over time. No, this adjuvant, or immune response enhancer molecule was known as “Freund’s Complete Adjuvant” and was used in animal experimentation to produce cataclysmic and lethal auto immune disorders in animals. 100% of the time when they were injected.
Fast forward to today’s news: On September 15, 2009 Health and Human Services Secretary Kathleen Sebelius announced the approval, in the total absence of any safety testing, of 4 new vaccines for the novel A/H1N1 Swine Flu virus which allegedly appeared in Mexico this past April for the very first time in the world’s history.
But wait! Patents for this vaccines “against” this very virus were applied for by Medimmune (parent company to Sanofi Aventis), Novartis and Baxter International. Baxter and Novartis applied for patents using squalene-based adjuvants. Baxter and Novartis’ adjuvant of choice is called MF59, detailed in the article below as a powerful – and highly toxic – squalene compound. GSK’s adjuvant, MLP(AS04) [also identified as AS03 in company statements and, like AS01 and 2, contains MLP, or, in simple terms, squalene] is also a powerful and literally poisonous auto immune stimulant made from squalene.
Baxter knows that, as far as immune enhancement to prevent disease goes, squalene adjuvants do not even work. So we have to wonder if – hard, strong and long, if the introduction of squalene has anything to do, anything at all, with the avowed goal of preventing a pandemic.
Quoting Investigative Report Jane Burgermeister,
“On July 13th, WHO ordered the inclusion of oil-in-water adjuvants in the “swine flu” H1N1 vaccines to be distributed throughout the world this autumn on the recommendation of its vaccine advisory panel, packed with Baxter and pharmaceutical executives, in spite of the fact that clinical studies published by Baxter’s own scientific team that patented the H1N1 vaccine demonstrate that such adjuvants are, at best, useless.
‘SAGE [WHO’s advisory panel on Pandemic Vaccines, on which Baxter and other vaccine manufacturers sit – REL] recommended that promoting production and use of vaccines such as those that are formulated with oil-in-water adjuvants and live attenuated influenza vaccines was important,’ says the WHO pandemic briefing note.
In June 2008, Baxter’s Austrian-based scientists Ehrlich, Kistner and Barret published a clinical trial in the New England Journal of Medicine ((Previous Volume 358:2573-2584 June 12, 2008 Number 24) on the safety of an H5N1 whole-virus vaccine, in which they themselves go on record saying that the use of adjuvants did not improve the antibody response.
In spite of the evidence that adjuvants are at best useless, vaccine companies such as Baxter and Novartis are rolling out vaccines which contain adjuvants like squalene (MF59), a substance added to the anthrax vaccine given to US soldiers, causing tens of thousands of Iraq Desert Storm soldiers to suffer permanent neurological damage.
Also, WHO is reported to have advised the use of “antigen sparing” protocols which means they are calling for the use of not much virus and lots of adjuvant.
The effects of adjuvants are so destructive to the human body that some people say that adjuvants are part of the next generation of biological or pharmacological warfare.”
In Squalene: Be Afraid, Part II we will discuss what the underlying reason for this adjuvant and document why the greatest danger in this Pandemic may not even be the vaccine we all have so much reason to fear.
A Glimpse into the Scary World of Vaccine Adjuvants
By Edda West – Published in VRAN Newsletter – Winter 2005
Adjuvants are formulated compounds, which when combined with vaccine antigens intensify the body’s immune response. They are used to elicit an early, high and long-lasting immune response. “The chemical nature of adjuvants, their mode of action and their reactions (side effect) are highly variable in terms of how they affect the immune system and how serious their adverse effects are due to the resultant hyperactivation of the immune system. While adjuvants enable the use of less *antigen to achieve the desired immune response and reduce vaccine production costs, with few exceptions, adjuvants are foreign to the body and cause adverse reactions”, writes Australian scientist Viera Scheibner Ph.D, (1)
The most common adjuvant for human use is an aluminum salt called alum derived from aluminum hydroxide, or aluminum phosphate. A quick read of the scientific literature reveals that the neurotoxic effects of aluminum were recognized 100 years ago. Aluminum is a neurotoxicant and has been linked to Alzheimer’s disease and other neurological disorders. Prior to 1980, kidney patients undergoing long term dialysis treatments often suffered dialysis encephalopathy syndrome, the result of acute intoxication by the use of an aluminum-containing dialysate. This is now avoided using modern techniques of water purification. In preterm infants, prolonged intravenous feeding with solutions containing aluminum is associated with impaired neurologic development. Scientists speculate that aluminum neurotoxicity may be related to cell damage via free radical production, impairment of glucose metabolism, and effects on nerve signal transduction. (2) Vaccines which contain both aluminum adjuvants and mercury based preservative, greatly magnify the neurotoxic effects. (3)
Macrophagic myofasciitis (MMF) is a muscle disease first identified in 1993, and has been linked to vaccines containing aluminum adjuvants. Muscle pain is the most frequent symptom which can be localized to the limbs or be more diffuse. Other symptoms include joint pain, muscle weakness, fatigue, fever, and muscle tenderness. The disorder is associated with an altered immune system in some, but not all patients. A study published in the journal Brain (2001) revealed that 50 out of 50 patients had received vaccines against hepatitis B virus (86%), hepatitis A virus (19%) or tetanus toxoid (58%), 3-96 months (median 36 months) before biopsy. “We conclude that the MMF lesion is secondary to intramuscular injection of aluminum hydroxide-containing vaccines, shows both long-term persistence of aluminum hydroxide and an ongoing local immune reaction, and is detected in patients with systemic symptoms which appeared subsequently to vaccination”, write the authors of the study. (4)
But aluminum’s neurotoxicity is of less concern to the vaccine industry than the fact that it elicits a lesser antibody response to the so called purer recombinant or synthetic antigens used in modern day vaccines than in older style live or killed whole organism vaccines. “This has created a major need for improved and more powerful adjuvants for use in these vaccines.” (5)
For decades, vaccine developers have been tinkering with various substances to trick the body into heightened immune responses. The most effective adjuvants are formulated with oils but have long been considered too reactive for use in humans. Immunologists have known for decades that a microscopic dose of even a few molecules of adjuvant injected into the body can cause disturbances in the immune system and have known since the1930’s that oil based adjuvants are particularly dangerous, which is why their use has been restricted to experiments with animals.
The classic oil based adjuvant called Freund’s Complete Adjuvant can cause permanent organ damage and irreversible disease – specifically autoimmune diseases. When scientists want to induce autoimmune disease in a lab animal, they inject it with Freund’s Complete Adjuvant, which causes great suffering and is considered by some too inhumane to even inject into animals.
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. (6)
Adjuvants can break “tolerance”, meaning they can disable the immune system to the degree that it loses its ability to distinguish what is “self” from what is foreign. Normally, the immune system ignores the constituents of one’s own body. Immunologists call this “tolerance”. But if something happens to break “tolerance”, then the immune system turns relentlessly self-destructive, attacking the body it is supposed to defend. (6)
Scientists theorize that oil based adjuvants have the ability to “hyperactivate” the immune system, and in doing so, create chaos by inducing such an extremely powerful response that the immune system literally goes haywire and starts attacking elements it would normally ignore. (6)
Another theory has to do with “specificity”. One of the great distinguishing characteristics of the immune system is something akin to a highly sensitive innate intelligence that has evolved over eons to be able to respond very precisely to what it deems to be a threat to the body. Because the body contains many types of oily molecules and lipids, it may be that when an oil is injected, the immune system responds to it not only specifically, but with heightened intensity because the oil adjuvant resembles so closely the natural oils found in the body. A “cross reaction” then happens, sending the immune system into chaos destroying any oils found anywhere in the body that resemble the adjuvant oil. Demyelinating diseases like multiple sclerosis are an example of this destructive autoimmune process. (6)
To deepen one’s understanding of the shadowy world of vaccine development, award winning investigative journalist Gary Matsumoto’s new book is a “must read.” It documents the secret human medical experimentation conducted on American citizens by doctors and scientists working for the U.S. military. It is a book about “betrayal of the most fundamental rules of medical ethics; and betrayal of the basic duty of military and civilian leaders to protect the people they govern.” Vaccine A: The Covert Government Experiment That’s Killing our Soldiers and Why GI’s are Only the First Victims, is a gripping read into the mad science world of the U.S. military’s biowarfare vaccine development program which, since 1987 has injected tens of thousands of U.S. troops with an experimental unlicensed anthrax vaccine containing squalene. An oil based adjuvant, squalene has been known for decades to cause severe autoimmune diseases in laboratory animals. Writes Matsumoto, “The unethical experiments detailed in this book are ongoing, with little prospect of being self-limiting because they have been shielded from scrutiny and public accountability by national security concerns.” Reading this book, one gets a permanent chill in the spine as we glimpse the “writing on the wall” of what is to come. (6,7)
“When UCLA Medical School’s Michael Whitehouse and Frances Beck injected squalene combined with other materials into rats and guinea pigs back in the 1970’s, few oils were more effective at causing the animal versions of arthritis and multiple sclerosis”, writes Matsumoto. In 1999, Dr. Johnny Lorentzen, an immunologist at Sweden’s Karolinska Institute proved that on injection, “otherwise benign molecules like squalene can stimulate a self-destructive immune response”, even though they occur naturally in the body. Other research institutes have also shown that the immune system makes antibodies to squalene, but only after it is injected (6) We now know that squalene, added to boost immune response in a formulation known as MF59, is the secret ingredient in certain lots of experimental anthrax vaccine that has caused devastating autoimmune diseases and death in countless Gulf War vets (Canadian, British and Australian troops were also injected with squalene laced vaccine), and continues to be used today. There is a “close match between the squalene-induced diseases in animals and those observed in humans injected with this oil: rheumatoid arthritis, multiple sclerosis and systemic lupus erythematosus”, writes Matsumoto. These three illnesses have been proven to be caused by this oil, but there is an additional long list of autoimmune diseases associated with squalene injection into humans. (6) “There are now data in more than two dozen peer-reviewed scientific papers, from ten different laboratories in the U.S., Europe, Asia and Australia, documenting that squalene-based adjuvants can induce autoimmune diseases in animals..observed in mice, rats, guinea pigs and rabbits. Sweden’s Karolinska Institute has demonstrated that squalene alone can induce the animal version of rheumatoid arthritis. The Polish Academy of Sciences has shown that in animals, squalene alone can produce catastrophic injury to the nervous system and the brain. The University of Florida Medical School has shown that in animals, squalene alone can induce production of antibodies specifically associated with systemic lupus erythematosus”, writes Matsumoto. (6)
Long List of Side Effects Referring to squalene in her extensive article on adjuvants, Dr. Scheibner writes, “This adjuvant contributed to the cascade of reactions called “Gulf War syndrome”, documented in the soldiers involved in the Gulf War. The symptoms they developed included arthritis, fibromyalgia, lymphadenopathy, rashes, photosensitive rashes, malar rashes, chronic fatigue, chronic headaches, abnormal body hair loss, non-healing skin lesions, aphthous ulcers, dizziness, weakness, memory loss, seizures, mood changes, neuropsychiatric problems, anti-thyroid effects, anemia, elevated ESR (erythrocyte sedimentation rate), systemic lupus erythematosus, multiple sclerosis, ALS (amyotrophic lateral sclerosis) also known as Lou Gehrig’s disease, Raynaud’s phenomenon, Sjorgren’s syndrome, chronic diarrhea, night sweats and low-grade fevers. (1)
Matsumoto punctuates his book with poignant interviews of military personnel who suffered many of these extreme and devastating syndromes, all of whom tested positive for anti-squalene antibodies which has become THE definitive marker for people who have been injected with this adjuvant and who have gone on to develop catastrophic diseases.
Immunologist, Dr. Pamela Asa was the first person to recognize that the autoimmune diseases she was seeing in military personnel mirrored those in experimental animals injected with oil formulated adjuvants. When she met a patient with similar autoimmune symptoms who had participated in an experimental herpes vaccine trial, who also knew he had been injected with MF59, a squalene adjuvant being used as a ‘placebo’ in that study, everything began to fall into place. Pam Asa contacted Dr. Robert Garry, a leading virologist at Tulane University Medical School, whose specialty is developing antibody tests and asked him to develop a test for the detection of anti-squalene antibodies – a test that ultimately became the most important forensic and diagnostic tool identifying patients whose autoimmune diseases followed injection with squalene laced anthrax vaccine. (6)
Juxtaposed to heart wrenching testimonies of shattered health and ruined lives is the military’s defiant stonewall and denial that a squalene laced anthrax vaccine was injected into thousands of its people without their informed consent – this despite the fact that the FDA and independent researchers have tested and identified varying amounts of squalene in specific lots of the vaccine.
Even more stunning is the fact that by 1997, hundreds of millions of dollars had already been spent testing vaccines formulated with squalene adjuvants by leading research institutes like NIH (National Institutes of Health) who tested its efficacy in HIV vaccines, the National Cancer Institute who for nearly two decades conducted research with squalene-boosted vaccines, and the National Institutes of Allergy and Infectious Diseases (NIAID) had been testing it in animals since 1988 and began human clinical trials in1991. Nineteen of NIAID’s 23 trials were for prototype HIV vaccines. Writes Matsumoto, ” Squalene adjuvants are a key ingredient in a whole new generation of vaccines intended for mass immunization around the globe.” (6)
Immune System Sees Squalene as an Enemy to Attack Researchers at Tulane Medical School and the Walter Reed Army Institute of Research “have both proven that the immune system responds specifically to the squalene molecule. Squalene’s pathway through the body has been tracked with a radioactive tracer in animals by none other than Chiron, (well known flu vaccine manufacturer) and maker of MF59, the squalene-based adjuvant, now also a component of FLUAD, an Italian influenza vaccine. (6)
The immune system does in fact “see” squalene and recognizes it as an oil molecule native to the body. The key is “route of administration”. As Gary Matsumoto says, “Squalene is not just a molecule found in a knee or elbow – it is found throughout the nervous system and the brain.” When it is injected into the body, the immune system sees it as an enemy to be attacked and eliminated.(6)
As any immunologist will tell you, the way an antigen encounters the immune system makes all the difference. You can eat squalene – no problem as it is an oil the body can easily digest. But studies in animals and humans show that injecting squalene will “galvanize the immune system into attacking it, which can produce a self-destructive cross reaction against the same molecule in the places where it occurs naturally in the body – and where it is critical to the health of the nervous system.” (6)
This phenomenon is also known as ‘molecular mimicry’, where the immune system forms antibodies against one of its own structures and will continue to attack the ‘self’ molecule in the body that resembles the one in the germ, or as is the case with squalene, an identical substance that is naturally present in the body. Once this self-destructive process begins, it never stops as the body continues to make the molecule the immune system is now trained to attack.
Another example involving autoimmune ‘molecular mimicry’ is when the immune system has been sensitized to attack myelin, the insulating fatty coating around nerve fibers which insures the smooth relay of nerve signals. The body would continue to make myelin in order to replenish and repair the protective sheath around its nerve endings. But says Matsumoto, “In the act of doing so, the body immunizes itself against itself, administering over and over again what amounts to a booster dose of something that the immune system now wants to get rid of. This vital constituent (myelin) is now the enemy, and the immune system is now programmed to obliterate it in an endless loop of self-destruction” – the process involved in MS (multiple sclerosis), and ALS (Lou Gehrig’s disease).(6)
Tying molecular mimicry to the autism epidemic, many children have regressed into autism spectrum disorders after injection with the triple live virus MMR (measles,mumps,rubella) vaccine. Dr.Vijendra Singh’s research at Utah State University suggests that auto-antibodies are attacking myelin in these children. He has shown that many autistic children have auto-antibodies to brain myelin basic protein (MBP) as well as elevated levels of measles virus antibodies. “Immunoblotting analysis showed the presence of an unusual MMR antibody in 60% (75 of 125) of autistic children, but none of the 92 normal children had this antibody. In addition, there was a positive correlation (greater than 90%) between MMR antibody and MBP auto-antibody, suggesting a causal association between MMR and brain autoimmunity in autism. This is one of the most important findings in autism to date, which prompted us to link measles virus in the etiology of the disorder”, writes Dr. Singh. (8,9,10)
Immunologist Dr. Bonnie Dunbar has also done extensive research on the mechanisms of injury inflicted by hepatitis B vaccine and has observed similar autoimmune processes involving molecular mimicry in people who developed devastating neuroimmune syndromes after injection with this vaccine. (11)
Molecular Mimicry as a Bio-Weapon Matsumoto reports that Soviet bioweaponeers used the principal of molecular mimicry in the 1980’s to engineer a ‘designer disease’ that would attack myelin. By splicing a fragment of myelin basic protein into legionella bacterium, they created what amounted to a living “nano-bomb”, which they injected into guinea pigs. What they found was that the immune system quickly cleared the legionella bacterium, but the myelin molecule, smuggled in by this microbial “Trojan horse” initiated a second wave of disease which caused experimental allergic encephalomyelitis, the animal version of MS. The Soviets recognized this creation for what it was – a biological time bomb!! (6)
“Squalene is a kind of trigger for the real biological weapon: the immune system. When the immune system’s full repertoire of cells and antibodies start attacking the tissues they are supposed to protect, the results can be catastrophic,” writes Matsumoto. His assessment is seconded by Dr. Pam Asa – “Oil adjuvants are the most insidious chemical weapon ever devised.” (6)
“Molecular mimicry, seen for its diabolical potential as a weapon by the Soviets as far back as the 1980’s, also applies to squalene. But the real problem with using squalene, of course, is not that it mimics a molecule found in the body; it is the same molecule,” writes Matsumoto. “So what American scientists conceived as a vaccine booster was another “nano-bomb”, instigating chronic, unpredictable and debilitating disease. When the NIH (National Institutes of Health) argued that squalene would be safe because it is native to the body, just the opposite was true. Squalene’s natural presence in the body made it one of the most dangerous molecules ever injected into man!” (6)
The main proponents for the use of squalene in vaccines have been the U.S Department of Defense and the NIH. The anti-squalene antibodies in sick American and British military personnel are evidence that military experimentation has caused an unprecedented health catastrophe in tens of thousands of people onto whom the vaccine was forced and who were denied the right to make an informed decision based on existing scientific knowledge of the dangers of injecting squalene. “By adding squalene to their new anthrax vaccine, they did not make a better vaccine, they made a biological weapon.” (6) .
Why , one would obviously ask, would anyone knowingly inject such a dangerous substance into humans? Certainly in terms of the U.S. military’s decision, they chose to turn a blind eye to the existing science, which for decades had documented the immune destructive properties of squalene. They justified its use because they knew they had a weak and ineffective vaccine which needed a serious boost. In the face of weaponized biowarfare agents like anthrax already developed by Russia and fear that it was also possessed by Iraq, they were desperate to increase the vaccine’s effectiveness as they launched into the first Gulf War. Additionally, explains Matsumoto, “scientists in the United States are now literally invested in squalene. Army scientists who developed the second generation anthrax vaccine have reputations to protect and licensing fees to reap for the army..[and] .worldwide rights to develop and commercialize the new recombinant vaccine for anthrax.” (6)
He goes on to explain, “the National Institutes of Health (NIH) has been supporting both animal and human research with squalene since the 1980’s. Squalene has become perhaps the most ubiquitous oil adjuvant on the planet, which is something that should concern everyone. Many of the cutting edge vaccines currently in development by the NIH and its corporate partners contain squalene in one formulation or another. There is squalene in the prototype recombinant vaccines for HIV, malaria, herpes, influenza, cytomegalovirus and human papillomavirus. Some of these prototypes like HIV, malaria and influenza are intended for mass immunization around the globe.” (6)
Squalene Adjuvants Enter the Global Market FLUAD, the squalene boosted flu vaccine has been licensed in Italy since 1997. It contains MF59, the squalene adjuvant made by Chiron. Although all the published papers co-authored by Chiron-employed scientists and Italian researchers have reported MF59 to be safe, Gary Matsumoto suggests a flaw in study designs may “prevent researchers from seeing the vaccine’s real risks.” Testing of FLUAD was limited to elderly people in nursing homes – average age was 71.5 which would tend to obscure autoimmune problems that might arise for a number of reasons. If autoimmune symptoms like joint pain and fatigue did occur in geriatric Italians, doctors might not connect these complaints to anything but old age. (6)
“Autoimmunity is notorious for taking years to diagnose because the early symptoms (e.g. headaches, joint and muscle pain and fatigue) are so vague; primary care physicians often fail to recognize it…a large Phase lV trial did not even bother to analyze the “common-post immunization reactions” in study participants, recording only those adverse events severe enough to require a doctor’s visit within 7 days of immunization.” In another study patients were observed for 180 days, but only serious events like “admission to hospital or death” qualified as a reaction – nothing else was recorded. Symptoms of adverse reactions listed in the FLUAD package insert are almost identical to the Air Force case-definition for Gulf War Syndrome, and include rashes, malaise, fever, myalgia, arthralgia, weakness, sweating and various autoimmune reactions and neurologic disturbances. (6)
“The question is whether scientists working for pharmaceutical companies are intentionally designing studies so as to miss adverse reactions that inconvenience their marketing strategy?” asks Matsumoto. “Chiron’s conclusion about squalene’s safety are at odds with recent data from studies in both animals and humans.” (6)
Just in from the newslists on February 9, 2005 is an item informing of the European “debut” of a new adjuvant approved for use in a new high-potency hepatitis B vaccine. Fendrix, the new enhanced hepB vaccine is being launched by pharma giant GlaxoSmithKline for use in people with poor immune responses (like dialysis patients) and those at high risk for developing hepatitis B. It is formulated with a new adjuvant that can “significantly improve the effectiveness of immunizations.” AS04, the ‘proprietary’ adjuvant based on MPL, originally developed by U.S. company Corixa, “increases the immune potency of the new vaccine, allowing two dose administration rather than three. It has been shown clinically to be more effective than alum, the most widely used adjuvant in vaccines.” (12)
So what exactly is this new high potency adjuvant? We’re told by the press release that MPL (AS04), is a “derivative of the lipid A molecule found in Gram-negative bacteria, is extracted from bacterial cell walls and is one of the most potent regulators of the immune response, used by the body to alert itself to bacterial infections.”(12) Full name of the lipid is monophosphoryl lipid A (MPL)
This news should put everyone on high alert because guess what? Lipids are oils/fatty acids and according to Matsumoto, MPL is identified in declassified documents as one of two squalene emulsions used in the Army’s new “recombinant protective antigen anthrax vaccine (rPA) which the FDA, the National Institutes of Health (NIH) and the Department of Defense fast-tracked into clinical trials in1998. The other squalene adjuvant they used was Chiron’s MF59. (6)
It appears that Fendrix is only the first of a whole new generation of “enhanced potency” vaccines coming down the pipeline using the new high potency lipid adjuvant, MPL. “The adjuvant is also being used in a number of GSK’s developmental vaccines, including one that could be the first effective vaccine for malaria”, says the article. MPL (AS04) adjuvant is also a component of GSK Bio’s genital herpes vaccine, as well as a component in their cervical cancer vaccine and a new tuberculosis vaccine.” (12)
In the unraveling of the squalene story, we find that a squalene emulsion first known as Triple Mix (based on Freund’s adjuvant) was later given the commercial name “Ribi”. Triple Mix (renamed Ribi) was tested by Dutch scientists on rabbits who found it caused “severe effects the largest number and most severe lesions when compared with the other adjuvants.”(6) Then in June 1999, Ribi ImmunoChem its manufacturer was acquired by Corixa Corporation for $56.3 million, who presumably also own the Ribi formulation. Whether MPL(AS04) is a formula related to Ribi is undoubtedly “proprietary” information, but from Matsumoto’s reseasrch, we know they are all squalene based. And it doesn’t end there. MPL, Corixa’s multi-million dollar baby, is slated for inclusion not only in the “enhanced potency” vaccines already mentioned, but will also be a strategic component of new allergy and autoimmune vaccines in development. (13)
From their inception, mass vaccinations have acted as a biological weapon, undermining health, manipulating and crippling the immune system, and instigating cycles of new and debilitating diseases. Monopoly medicine’s solution? Inject us with more powerful, genetically engineered high potency vaccines. Never mind they are seeding us with “nano-bombs” that will further attack our already compromised immune systems.
The concept of stimulating a hyperactive immune response by using oil-based adjuvants has clearly backfired since we now know that the stronger the antigenic response, the more damaging the adjuvant itself is to the normal functioning of the brain and nervous system. The precedent for mass medical experimentation via an ever increasing recommended vaccine schedule has been set. We can now predict the grim future of mankind: an epidemic of neurological disorders and autoimmune diseases never before imagined.
Notes & Resources
Adjuvants listed by Scheibner: “Today the most common adjuvants for human use are aluminum hydroxide, aluminum phosphate and calcium phosphate. However, there are a number of other adjuvants based on oil emulsions, products from bacteria (their synthetic derivatives as well as liposomes) or gram-negative bacteria, endotoxins, cholesterol, fatty acids, aliphatic amines, paraffinic and vegetable oils. Recently, monophosphoryl lipid A, ISCOMs with Quil-A, and Syntex adjuvant formulations (SAFs) containing the threonyl derivative or muramyl dipeptide have been under consideration for use in human vaccines
*Definition of Antigen (Scheibner): “Micro-organisms, either bacteria or viruses, thought to be causing certain infectious diseases and which the vaccine is supposed to prevent. These are whole-cell proteins or just the broken-cell protein envelopes, and are called antigens”
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.
09/16/09 – News Flash! Dr. Ron Paul’s Congressional office confirmed this morning that the good doctor will introduce a vaccination bill in Congress shortly, to protect all Americans from forced vaccinations with un-safety tested ingredients. We will post an Action Item supporting the bill here as soon as it is filed, so please check here often.
Natural Solutions Foundation will appeal the FDA’s illegal approval of vaccines for a novel virus which have had no testing carried out for safety or effectiveness. We need your support. Here’s how:
1. Disseminate this information and urge everyone you can reach to take the action step above. There is little time left. Shots are set to begin in about 2 weeks.
2. Double Donate:
a. Give yourself and others shade grown Valley of the Moon(TM) Coffee, http://drrimatruthreports.com/?page_id=1130, get a $20 tax credit for each 8 oz bag you buy or give (including your corporate giving!) and help support the Natural Solutions Foundation. It’s Freedom’s Own Coffee: GMO-Free, Pesticide-Free, Toxin-Free and it supports YOUR health freedom by supporting Natural Solutions Foundation. Please help to Wake Up, America(TM) with Valley of the Moon(TM) Toxin-Free Coffee.
b. Make a recurring donation to our Legal Freedom Defense Fund with a tax deductible donation that ends in the number “6” AND make another to support the most effective health freedom organization in the world, Natural Solutions Foundation. Click here: http://drrimatruthreports.com/?page_id=189 now. Thanks!
September 15, 2009 – HHS Secretary Sebelius appeared today before the House Energy and Commerce Committee where she announced that the so-called “Swine Flu” vaccines were licensed today.No mention was made whether an Emergency Use Authorization under the Project Bioshield Act of 2005 was involved. She told Congress that www.flu.gov will have full details.
Rep deGette asked about adjuvants and the Secretary said “no adjuvants are currently anticipated” to which she added, “the scientists don’t want to head down that path.”*
[By the way, the quotes and notes are from our Eyes in DC, Maury Silverman. Maury attends hours of government hearings and plies the Halls of Congress for health and freedom. Thanks, Maury, for being the Eyes and Ears of Health Freedom in the meeting rooms and halls of Washington.]
According to his notes, Sebelius said, “5 facilities are currently to be licensed” and “FDA has approved vaccine applications.” This announcement was made about 2 PM today. [Note that plural applications have been approved, according to the Secretary – RF]
Secretary Sebelius also opined, “The influenza is going to be unpredictable…”
Rep Markey of Massachusetts questioned “Swine Flu” vaccines’ safety compared to the 1976 “Swine Flu” vaccine. Sebelius said the government gathered the experts from 1976 to consult and is not concerned about safety questions. [We, on the other hand, are concerned enough about the safety questions to continue our legal challenge to this unprecedented and enormously unwise action by the FDA – RF]
[Note: this position of the Secretary is consistent with comments by FDA figures, for example:
“Norman Baylor, PhD, director of FDA’s Office of Vaccines Research and Review, explained the FDA’s probable decision to go ahead with the simplified approval process, rather than a lengthy new drug application process. “We have decades of experience with H1N1, that’s why we feel we can do this with a strain-change [rather than a full drug application process – RF],” said Dr. Baylor.” http://www.medpagetoday.com/ProductAlert/DevicesandVaccines/15230
The only time the government previously approved a “Swine Flu” vaccination was during the 1976 fiasco, resulting in hundreds of deaths and thousands maimed for life, all for a pandemic that never happened. That’s the government’s “experience” that gives rise to their false claim that these vaccines, according to them for a “novel” virus, do not need comprehensive safety testing – RF]
Continuing, the HHS Secretary outlined a central distribution system of the vaccines from the 5 approved facilities to 90,000 predetermined sites. The distribution system will be run by a single contractor. The Agency has allocated $1.44 billion allocated to the States to operate the vaccine program. She further claimed there will be enough vaccine to all who “need it” and people should consult their physicians.
These vaccines have the dubious distinction of being approved for what the government has claimed was a “novel” flu virus under a “change of strain” review that is never used for novel diseases. Thus the FDA has violated the requirement of Title 21 of the US Code that new drugs must be shown, with significant scientific agreement, to be both safe and effective, with the benefits outweighing the risks. Without comprehensive safety testing, how can that standard be met?
See the Natural Solutions Foundation’s most recent Citizens Petition which sought to stop approval of the vaccines and which will now form the basis of a Court appeal to reverse their licensing. This Citizens Petition, which sought emergency relief from the FDA, was accepted as an emergency Petition but the FDA gave itself 180 days to deal with it, clearly anticipating that this action would make our Petition irrelevant as a tool to stop the H1N1 flu shots. http://drrimatruthreports.com/?p=3314
Ralph Fucetola JD
Natural Solutions Foundation
Counsel and Trustee
* Note: We don’t particularly trust the Secretary’s intent to avoid adjuvants and know that the US purchased nearly a half billion dollars worth of squalene, according to an HHS press release of July 13, 2009 — http://www.hhs.gov/news/press/2009pres/07/20090713b.html. We do agree, this time, with their scientists! Push Back Works!
Donate:http://drrimatruthreports.com/?page_id=189 Support Court Challenge to Prevent FDA from Approving Swine Flu Vaccines Before Safety Testing is Complete (July 2010) -make your recurring tax deductible donation ending in the number “6” to earmark it for the legal fund
Make your recurring tax deductible donation ending in any other number to support the Natural Solutions Foundation
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.