Archive for Self Quarantine – Page 2
MEDIA RELEASE
Natural Solutions Foundation
The Voice of Global Health Freedom™
http://www.GlobalHealthFreedom.org/
October 15, 2009 Update: Motion for Injunction filed: http://drrimatruthreports.com/?p=3657
For Immediate Release:
“STOP THE SHOT” Litigation Filed
Health Freedom Advocates and NY Health Care Workers
Seek Protection from DC Federal Court in
Legal Effort to Void FDA Swine Flu Vaccine Approval
Washington DC – October 9, 2009: Despite the FDA’s intention to begin delivery this week of the n ovel “Swine Flu” 2009-H1N1-A live virus nasal mist vaccine to 90,000 government-approved locations nationwide, six New Yorkers and several NonGovernmental Organizations (NGOs) filed for an Emergency Injunction in the US District Court for the District of Columbia to prevent the distribution of what they believe are illegal, unnecessary and dangerous vaccines.
The case of Null, Laibow et al. v FDA et al. [Docket No. 1:09-cv-01924]challenges the legality of the September 15th licensing of four vaccines prior to any safety testing for what the government calls a “novel flu virus with pandemic potential.” The complaint alleges that the government failed to follow its own rules and applicable legislation in rushing the vaccine approvals in the absence of any of the requisite minimum scientifically sound and appropriate testing for both safety and effectiveness as required by law since 1964.
Link to Complaint:http://drrimatruthreports.com/?page_id=3619
Link to Brief: http://drrimatruthreports.com/?page_id=3624
Link to Action eAlert: http://drrimatruthreports.com/?p=3635
Link to “I’m Not a Pharma Serf” Action Item: http://bit.ly/4FxB4r
The New Yorkers are all health care workers who are therefore subject to that State’s new legal mandate (promulgated August 13, 2009) requiring that nearly all of the State’s half million health care workers receive all Federally recommended flu vaccines or lose their jobs. This requirement puts the health care workers in significant jeopardy since these newly approved vaccines have never been tested for either safety or efficacy and may carry major risks.
The lawsuit, announced at a demonstration by the health care workers last week at the State Capitol in Albany on September 29, 2009, is expected to be just one of the suits filed challenging various government “emergency” actions for a flu that has proven (during the just concluded Southern Hemisphere flu season) to be neither pandemic nor virulent despite dire predictions to the contrary and despite a Health Emergency declared by the CDC on April 25, 2009, 11 days after the first alleged death from Swine Flu on April 14, 2009 and a Level 6 Pandemic declaration by the World Health Organization followed on June 11, 2009 (which was only possible since W.H.O. downgraded the definition of a “Level 6 Pandemic”).
The Plaintiffs include health care professionals such as Dr. Gary Null, PhD, a well-known New York nutritionist, Rima E. Laibow, MD, a New York licensed physician who is Medical Director and a Trustee of the Natural Solutions Foundation, Dr. Tedd Koren DC, head of Foundation for Health Choice and four other health care workers covered by the mandate, including a Registered Nurse who has had prior adverse reactions to flu vaccines; a pregnant Nurse’s Aide, a health care student who has been told that she cannot see the patients whom she must see in order to finish her training, and a woman who works in the billing department of a hospital. All have been denied exemptions and told they will lose their positions under the new mandate if they are not vaccinated with all flu vaccines, including the new “Swine Flu” vaccine.
The Complaint alleges that the FDA erred in determining that safety testing was not needed because the 2009-H1N1-A vaccines are a mere “change of strain” not requiring safety testing. The Plaintiffs claim there is no significant scientific agreement that supports the government’s actions. The experts presented by the Plaintiffs include Sarah Schon MD, a Board Certified Immunologist and Paul G. King PhD, a noted analytical chemist with decades of experience in the pharmaceutical industry.
The Plaintiffs further allege that the Live Attenuated Influenza Virus (LAIV) nasal mist vaccine could trigger the very pandemic the government claims people should fear, calling the decision to allow a LAIV vaccine using a WHO and CDC declared “novel pandemic virus” an “arbitrary and capricious decision without any basis in the scientific record.”
Citing HHS Secretary Sebelius’s September 15th testimony before a Congressional committee when she announced the vaccine licensing, that even the FDA’s own scientists would not “sign-off” on the use of the most toxic vaccine ingredients (known as “oil in water adjuvants”) the Plaintiffs allege the government has a plan to nonetheless approve these substances, never before approved for drug use in the United States, under an “Emergency Use Authorization” (EUA) permitted by the 2005 Project Bioshield Act. On July 13, 2009, according to a press release on the www.HHS.gov web site, the government purchased nearly a half billion dollar’s worth ($485 Million USD) of the deadly adjuvnt squalene, an oil in water adjuvant, blamed by many nongovernmental physicians as a “Gulf War Syndrome” causative agent in more than 25% of the soldiers who were subjected to an experimental anthrax vaccine, Vaccine A, containing squalene. Vaccine A was later authorized under an EUA propmpting a Court ruling that makes its use legal only in voluntary situations. The government’s stockpile is enough squalene to “stretch” the 167 million doses of “Swine Flu” vaccine the government has purchased to cover the entire American population since the purpose of an adjuvant is to increase immune response to the injected material. The FDA web site indicates that the adjuvanted vaccines will be provided under an EUA which will allow the agency to skirt “Good Manufacturing Practices” and any issue of whether squalene is too dangerous to be permitted.
Secretary Sebelius further testified before Congress that a single company will be contracted by the government to deliver the vaccines to 90,000 locations around the country. The FDA site further indicates that the squalene will be mixed with the approved vaccines at those sites before administering the shots, without regard to normal pharmaceutical manufacturing requirements. The Plaintiffs claim that this will result in dangerously adulterated vaccines that may cause much more injury than the infamous 1976 “Swine Flu” vaccine program that killed hundreds and maimed thousands before it was stopped just ten weeks after it began, with nearly fifty million Americans having received that deadly shot or the dangerous squalene-adjuvanted Vaccine A which caused so many cataclysmic illnesses and deaths in Gulf War I military personnel. These shots, too, were both unnecessary and untested.
In their submitted Complaint, Brief and Certifications the Plaintiffs remind the Court that as early as 1905, even before the Federal authorities had the legal power to license vaccines, the Supreme Court stated, in Jacobson v Massachusetts (197 U.S. 11),
“We are not to be understood as holding … that the judiciary would not be competent to interfere and protect the health and life of the individual … ‘All laws,’ this court has said, ‘should receive a sensible construction. General terms should be so limited in their application as not to lead to injustice, oppression or absurd consequence.’ …”
The lead attorney for the Plaintiffs, Leslie Fourton JD, of New York, is working with the respected Washington regulatory law firm of Swankin and Turner and a team of legal experts from around the country, including Larry Becraft JD, Alabama, Alan G. Phillips JD, North Carolina, and Ralph Fucetola JD, New Jersey.
Counsel Fourton stated,
“Without taking into account serious objections raised by many scientists, FDA approved four “Swine Flu” 2009-H1N1-A Vaccines without enough concern about any definitive safety testing and the quality thereof. The Secretary of Health and Human Services testified before Congress, announcing the approvals and a program to widely distribute the Vaccines which were purchased by the federal government. The administrative record appears to be defective in that the record as posted on the Agency web site does not include, for all the approved Vaccines, a drug package insert or label with an accurate list of ingredients. We don’t know what was approved or how dangerous it may be. The Plaintiffs seek immediate relief.”
The nongovernmental organizations who are supporting the New Yorkers threatened by the “Swine Flu” vaccine approvals, by joining in the legal action, are the National Solutions Foundation (www.HealthFreedomUSA.org), whose President is Maj Gen Bert Stubblebine (US Army Ret.), Dr. Tedd Koren’s Foundation for Health Choice (www.FoundationforHealthChoice.com) and the Gary Null organization (www.GaryNull.com).
For further information contact:
Ralph Fucetola JD – 973-300-4594
Natural Solutions Foundation Counsel and Trustee
ralph.fucetola@usa.net
This Media Release is being posted at: PRWEB – Tracking Number 3023904
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WHO Developing Infertility Vaccines since 1974. Is Swine Flu Vaccine the Next Generation?
URGENT ACTION ITEM for everyone you can reach: Say “NO!” to “Voluntary” vaccines when refusal means incarceration and indefinite quarantine. http://salsa.democracyinaction.org/o/568/campaign.jsp?campaign_KEY=27275 Sign once for every member of your household, then activate your community of influence.
Natural Solutions Foundation suing FDA to prevent release of Swine Flu vaccines. We’ll be entering our papers this week. We are restricting our suit to a narrow objection although we know that the vaccines are genocidal (see below) and worse. But we have to use what the law gives us and that is the fact that the law was broken on September 15, 2009 when the vaccines were licensed without any safety testing being completed (or even carried out).
Be aware that we are not satisfied with a mere delay, but it is where we start tactically. Winning this suit would prevent the release of the vaccines until next June or July, 2010. That is not shabby since it would give us time for more permanent action.
Federal Court Cases are expensive! Please make two recurring tax deductible donations, large or small: Click here, http://drrimatruthreports.com/?page_id=189, to make a donation ending in the number 6 to earmark you donation for the legal case. Now click the link again and make a donation ending in any other number to support the Natural Solutions Foundation so we can continue to serve you and help keep health freedom free. Thanks!
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OK. Now for the tough stuff
The article below details the horrific reality that I wish were not true. The Natural Solutions Foundation has been saying for quite some time that we see clear evidence of a genocidal intention in the overblown, clearly intentional Swine Flu “Pandemic”. When WHO moved the “Pandemic” from Level 4 to Level 5 the disease was so mild and inconsequential that they literally had to change the definition of a Pandemic at Level 5, leaving out the words “with the ability to cause serious illness and death” from the definition because it did not and could not. We believe that this must have been a great disappointment to the folks at the WHO who have been both predicting and involved with genetically engineering one failed pandemic after another. But WHO, you will remember, believes in a “sustainable planet” and that sustainability (favor them, not us, of course) means that they believe, too, that 90% of the world’s population needs to die.
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.
Knowing that:
– 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.
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.HealthFreedomusa.org
www.GlobalHealthFreedom.org
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Saturday, August 8, 2009
“Swine flu” vaccine has adjuvants that impair fertility, Making people infertile is part of eugenics, thus genocide.
http://dprogram.net/2009/08/07/“swine-flu”-vaccine-has-adjuvants-that-impair-fertility/
August 7, 2009
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.
Also, a Czech translation of “Evidence-of-the-Use-of-Pandemic-Flu-to-Depopulate-USA” can be found here: http://www.outsidermedia.cz/Obvinuji-Vas-z-masove-vrazdy-1.aspx
http://www.outsidermedia.cz/Obvinuji-Vas-z-pripravy-masove-vrazdy-II-1.aspx
“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.”
Abstract:
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.
http://www.wipo.int/pctdb/en/wo.jsp?wo=1999034825
Description:
http://www.wipo.int/pctdb/en/wo.jsp?IA=US1998027658&wo=1999034825&DISPLAY=DESC
__________________________________________________________
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
__________________________________________________________
Now, how can WHO claim the adjuvants is harmless:
http://www.who.int/vaccine_safety/topics/adjuvants/squalene/questions_and_answers/en/index.html
when there is clear evidence of its effects provoking AI diseases:
ANTI-SQUALENE ANTIBODIES LINK GULF WAR SYNDROME TO ANTHRAX VACCINE
http://www.autoimmune.com/GWSGen.html
or
“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”
Daniel Solis, Prague, Czech Republic
http://www.denikpolitika.cz/politici/daniel-solis/blog#31
http://www.czechfp.cz/site/?p=8009
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
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.
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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.
http://www.who.int/csr/disease/swineflu/notes/h1n1_vaccine_20090713/en/index.html
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.
http://content.nejm.org/cgi/content/short/358/24/2573In 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.
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
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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”
1.Viera Scheibner, Ph.D, The Adverse Effects of Adjuvants in Vaccines, Nexus Magazine Dec. 2000 vol.8, No.1
http://www.whale.to/vaccine/adjuvants.html
2. Aluminum Toxicity notes from Dr. Boyd Haley Toxic Test Foundation website: http://www.altcorp.com/DentalInformation/aluminumvaccines.htm
3. Boyd E. Haley, Professor of Chemistry: Thimerosal Containing Vaccines and Neurodevelopment Outcomes: http://64.41.99.118/vran/vaccines/mercury/mer_haley.htm
4. Brain, Vol. 124, No. 9, 1821-1831, September 2001, 2001 Oxford University Press http://brain.oupjournals.org/cgi/content/abstract/124/9/1821
5 Vaccine Adjuvants: current state and future trends, Volume 82: Issue Immunology and Cell Biology http://www.blackwellpublishing.com/abstract.asp ?ref=0818-9641&vid=82&iid=5&aid=5&s=&site=1
6.Gary Matsumoto, Vaccine A-
-
The Covert Government Experiment That’s Killing our Soldiers and Why GI’s are Only the First Victims
7.Gary Matsumoto Press Release and biography: www.vaccine-a.com
8 Vijendra K Singh, Ph.D, Abnormal Measles Serology and Autoimmunity in Autistic Children – Journal of Allergy & Clinical Immunol, 109 (1): S232, January 2002
9. Vijendra Singh – lecture at ATEDM Conference: http://iquebec.ifrance.com/autismemtl/2002/program_en.html
10. Institute of Medicine Meeting (IOM) on Vaccines and Autism, February 9, 2004
11.. Bonnie Dunbar, Ph.D – articles and research proposal – VRAN website: http://64.41.99.118/vran/vaccines/hepatitis/dunbar_research.htm
12.New adjuvant debuts in new hep B vaccine , February 9, 2005, In-Pharma Technologist.com http://www.in-pharmatechnologist.com/news/news-ng.asp ?n=57959-new-adjuvant-debuts
13. Corixa weblink to MPL press release on allergy & autoimmune applications: http://www.corixa.com/default.asp?pid=auto_capsule&id=22
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Today there was a treat and a terror in my email box: a new article from William Engdahl. A treat, because William Engdahl is one of my heroes. I do not know whether to admire him most as a writer who researches or a researcher who writes. Looked at either way, however, he is an honest and fearless man whose works tell us what we need to know – and what the self-anointed elite does not want us to know. And they do so with passion, clarity but without the faintest hint of panic or hysteria.
A terror because of the subject: mercury and aluminum in our babies and our own bodies through the mechanism of vaccination. You have heard it before: mercury and aluminum are neurotoxins. The restatement of this information in the context of a clear and focused historical and scientific review of just what we are talking about when we talk about mercury, aluminum and autism. It must be read and shared.
There are a few more facts which help to frame the cataclysmic disaster called “Vaccine Injury”, which is by no means limited to children. Think for a moment of healthy young men and women in coma, developing demyelinating neurological disorders like MS, ALS (now seen in children and adolescents for the first time in history as a new disease called “Juvenile ALS, but only in girls and women who have received Gardasil), diabetes, encephalitis, meningitis, persistent and debilitating rashes, swollen, painful joints everywhere in the body, brain fog, memory loss, depression, loss of IQ, lupus and other auto immune disorders, Alzheimer’s Disease, etc.
They Would Have Died Anyway
Let’s start with the origins of Thimerisol, which is 49.6% mercury by weight. Mercury is more toxic by far to tissues, including the brain, than lead.
It was patented by Eli Lilly, a so called “ethical” drug company (so named because they sell patented medicines) in the 1920s. In 1930, it was administered IV to 22 meningococcal meningitis patients, all of whom were in coma. All 22 patients died.
Eli Lilly, an “ethical” drug company, concluded that Thimerisol was safe because although all patients died, none showed any adverse response to the injected Thimerisol since they WOULD HAVE DIED FROM OTHER CAUSES ANYWAY. Therefore, none died from Thimerisol and it was deemed to be safe. When the FDA was founded, this information was presented to it and accepted. Thimerisol was grandfathered into use. The FDA, always compliant to the desires of industry, bought the insane logic of the “ethical” drug company, to the endless tragedy of our children, our elders and ourselves. This horrific substance is added to our vaccines as a “preservative”.
As a simple side thought, if vaccine manufacturing were strictly clean and sterile, not careless, contaminated and dirty, why would a preservative be necessary? Thimerosal was subsequently introduced for use in vaccines and in over the counter remedies as a preservative to kill bacteria in the product without any additional safety testing of any kind since it had been “grandfathered”. The 1930 study, in which every patient died, remains the only safety testing done on the substance even after being in use for over 84 years.
Aluminum is added to vaccines in order to irritate the immune system and increase the production of antibodies which are ASSUMED to be associated with immune competence with respect to the disease entity on which the vaccine is focused. No compelling (or even non-compelling) scientific evidence exists which demonstrates that this type of antibody production is associated with protection from the disease. In fact, virtually every epidemic in modern times has occurred in fully vaccinated populations.
Aluminum is neurotoxic and is strongly associated with the epidemic of a previously unknown type of dementia which will impact more than half of those who reach the age of 80: Alzheimer’s Disease.
When combined with fluoride, also added to many vaccines, the two toxic metals are strongly synergistic, increasing the neurotoxicity of the other substance by many times, creating a much higher level of impact than either one alone could produce. Since nearly everyone in the US drinks fluoridated water and brushes their teeth with fluoride-containing toothpaste, even without added injected fluoride, the synergistic potential is both untested and very frightening.
These metals are not the only toxins found in vaccines, but they are, individually and in combination, enough to create the public health and private home tragedies which can be laid directly at the feet of Big Pharma and criminal regulators.
Please disseminate this blog as widely as possible with full attribution AND with the Action Items above: they are vital to our ability to stay unvaccinated, all of us, with the new and much deadlier Swine Flu vaccines. Safety testing, if you can call it that, will not be completed until July of 2010. Yet the WHO and FDA (CDC is part of FDA) are rushing to vaccinate our precious children, pregnant women and the chronically ill with a vaccine containing aluminum, mercury AND a million times more squalene than the wildly toxic anthrax Vaccine A which caused the horrific, and frequently lethal, Gulf War Syndrome in hundreds of thousands of Gulf War vets and is still causing the same damage in our soldiers now.
Despite that, the Department of Defense, Governor after Governor and employer after employer are making these untested vaccines mandatory even while the President and Secretary Sebelius of Health and Human Services intone solemnly that vaccinations will be “voluntary”, defining “voluntary” as one option of a pair of options which offer you the unsafe, untested, unnecessary and uninsurable vaccine, all liability for which both the government and the manufacturers have been relieve of in a convenient legislative and regulatory pirouette. The other option is involuntary internment or incarceration, as the public documents from Iowa, Florida, North Carolina and other states makes clear is already being prepared for you. Indeed, “vaccine refusers” in Massachusetts may, under a pending law, be liable to fines of $1000 per day for refusing to be vaccinated AND jailed for up to 30 days [Per day of refusal? For all days of refusal? – REL]
So, indeed, “it IS the Vaccines, Stupid!” as William Engdahl tells the FDA, the media and the rest of the deaf establishment.
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
Valley of the Moon(TM) Eco Demonstration Project
www.NaturalSolutionsFoundation.org
Valley of the Moon GMO and Toxin Free Coffee
www.ValleyoftheMoonCoffee.org
www.Organics4U.org
www.NaturalSolutionsMarketPlace.org
It’s The Vaccines Stupid!”
F. William Engdahl
Global Research
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.