Posts Tagged ‘Vaccination’

Vaccine Silly Season Heats Up: Vaccinate Children to Save Life Years!

Sunday, September 14th, 2008

The heat is on: against a growing background beat of “Pandemic’s nearly here, pandemic’s nearly here!” the repeated refrain of “Vet more vaccinations, get more shots!” is getting louder, too.

This time, we have a speculative paper that strikes me as absurd in which children are placed at high risk for getting vaccinated with yet more untested, potentially dangerous and very, very profitable vaccinations. In this case, the call is for saving the lives of children by vaccinating them with vaccines which contain deadly poisons like mercury, formaldehyde, fetal DNA, steal viruses, fluoride, chrolides, aluminum, etc., for a disease whose impact is vastly overstated (see “Flu Shot Does Not Reduce Risk of Death” following and not particularly the analysis of statistical conclusions about the death rate from flu. The highly absurd figure of 36,000 deaths per year from flu is used to sell flu vaccines and fear. But all, that’s right, all, deaths from pneumonia or any other possibly flu-related cause, whether it is or is not actually related to flu, is counted as a flu death in the grim sales pitch: get vaccinated or die.
As this second article cited shows, the reality, when examined closely, is nowhere near the puffery.
Well, what would you expect from a propaganda campaign?

Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
www.NaturalSolutionsFoundation.org
www.Organics4U.org
www.NaturalSolutionsMedia.tv
www.NaturalSolutionsMarketPlace.org

Vaccinating Younger Population Minimizes Life-Years Lost to Influenza

NEW YORK (Reuters Health) Sept 05 – Shifting the current vaccination strategy to target younger populations would reduce the number of years of life lost (YLL) to influenza, according to a report in the August 1st issue of The Journal of Infectious Diseases.

Vaccination allocation policy has been the subject of debate in light of several issues, among them the criticism by bioethicists of the inherent axiom that any life lost has the same value, regardless of the age of the deceased, the authors explain.

Dr. Mark A. Miller from the National Institutes of Health, Bethesda, Maryland, and colleagues sought to provide an alternative quantitative tool to help guide pandemic vaccine priority setting and achieve the greatest possible population impact, by preventing the loss of as many years of life as possible.

For a 1918-like pandemic scenario, in which most YLL occur for the younger age groups, the optimal vaccination group comprises people younger than 45 years, according to the models employed.

For a 1957-like epidemic, in which YLL were similar for older and middle age groups, it is unclear whether vaccinating the middle-age group would be better than vaccinating seniors, leading the investigators to conclude “that these age groups would be equally good choices.”

For a mild 1968-like influenza epidemic, the researchers note, vaccinating people 45 to 64 years old represents the optimal strategy for minimizing YLL.

“Our estimation is not an endorsement of any particular policy but highlights how the choice of health outcome metrics such as YLL can influence the prioritization of age groups to vaccinate in pandemic settings,” the authors explain. “It also shows that the vaccine priority scheme for seasonal influenza is not optimized to mitigate the impact of pandemic influenza.”

“These results suggest the need for pandemic plans to have an element of flexibility that allows the prioritization of age groups for immunization at the start of a pandemic to be modified as age-specific epidemiological data on the novel virus become available in real time,” the researchers conclude.

“Equally important, the question of who should be vaccinated first needs to be debated and reasoned through now, before the onset of a public health emergency, while we have the time to reflect on which decision-making metric is the most appropriate,” they add.

J Infect Dis 2008;198:305-311.

Flu Shot Does Not Reduce Risk Of Death, Research Shows

ScienceDaily (Aug. 31, 2008) — The widely-held perception that the influenza vaccination reduces overall mortality risk in the elderly does not withstand careful scrutiny, according to researchers in Alberta. The vaccine does confer protection against specific strains of influenza, but its overall benefit appears to have been exaggerated by a number of observational studies that found a very large reduction in all-cause mortality among elderly patients who had been vaccinated.

The study included more than 700 matched elderly subjects, half of whom had taken the vaccine and half of whom had not. After controlling for a wealth of variables that were largely not considered or simply not available in previous studies that reported the mortality benefit, the researchers concluded that any such benefit “if present at all, was very small and statistically non-significant and may simply be a healthy-user artifact that they were unable to identify.”

“While such a reduction in all-cause mortality would have been impressive, these mortality benefits are likely implausible. Previous studies were likely measuring a benefit not directly attributable to the vaccine itself, but something specific to the individuals who were vaccinated—a healthy-user benefit or frailty bias,” said Dean T. Eurich,Ph.D. clinical epidemiologist and assistant professor at the School of Public Health at the University of Alberta. “Over the last two decades in the United Sates, even while vaccination rates among the elderly have increased from 15 to 65 percent, there has been no commensurate decrease in hospital admissions or all-cause mortality. Further, only about 10 percent of winter-time deaths in the United States are attributable to influenza, thus to suggest that the vaccine can reduce 50 percent of deaths from all causes is implausible in our opinion.”

Dr. Eurich and colleagues hypothesized that if the healthy-user effect was responsible for the mortality benefit associated with influenza vaccination seen in observational studies, there should also be a significant mortality benefit present during the “off-season”.

To determine whether the observed mortality benefits were actually an effect of the flu vaccine, therefore, they analyzed clinical data from records of all six hospitals in the Capital Health region in Alberta. In total, they analyzed data from 704 patients 65 years of age and older who were admitted to the hospital for community-acquired pneumonia during non-flu season, half of whom had been vaccinated, and half of whom had not. Each vaccinated patient was matched to a non-vaccinated patient with similar demographics, medical conditions, functional status, smoking status and current prescription medications.

In examining in-hospital mortality, they found that 12 percent of the patients died overall, with a median length of stay of approximately eight days. While analysis with a model similar to that employed by past observational studies indeed showed that patients who were vaccinated were about half as likely to die as unvaccinated patients, a finding consistent with other studies, they found a striking difference after adjusting for detailed clinical information, such as the need for an advanced directive, pneumococcal immunizations, socioeconomic status, as well as sex, smoking, functional status and severity of disease. Controlling for those variables reduced the relative risk of death to a statistically non-significant 19 percent.

http://www.sciencedaily.com/releases/2008/08/080829091323.htm

Vaccine Failure Library: More Parents Question Vaccination

Wednesday, September 3rd, 2008

Vaccines have failed to gain universal trust because of their connection with illness and serious side effects including death and autism. Consumer confidence has been strongly shaken by coverups and denials, increased vaccinations and decreased government accountability.
The Vaccine Failure Library may, like all Natural Solutions Foundation materials, be used for non-profit purposes as long as full attribution is provided.
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
www.NaturalSolutionsFoundation.org
www.Organics4U.org
www.NaturalSolutionsMedia.tv
www.NaturalSolutionsMarketPlace.org

More Parents Question Vaccination
Vaccine poll highlights

In a Scripps Howard Survey conducted by the Scripps Survey Research Center of Ohio University via telephone survey during the period from September 24 to October 11, 2007, 811 adults were asked questions about vaccinations. Here are their answers as reported by Thomas Hargrove of the Scripps News Service

Respondents were asked Questions in Bold Face. Their answers follow each question.
Here are a few questions about vaccinations that children get to protect them from diseases like polio, mumps and measles. Most states require kids to receive up to 10 different vaccinations by the time they are five years old. Some parents and researchers say vaccines have side effects that may lead to autism, asthma, diabetes, attention deficit disorder and other medical problems. Have you heard about these concerns?
Yes, have heard …………… 66
No, have not heard ………… 33
Don’t Know/Other Response …… 1

Most U.S. health officials urge that children be vaccinated to protect them and to prevent the spread of disease. More than 1 million children die of measles outside the U.S. every year. Generally speaking, do you think the benefits of immunizations outweigh the risks or do you have questions about the risks of immunization?
Benefits outweigh risks ……. 71
Have Questions about risks …. 19
Don’t Know/Other Response ….. 10

Most states allow children to be exempt from vaccinations if their parents object for religious reasons. Many states also allow exemptions if parents are philosophically opposed to the vaccinations. Should parents be allowed to exempt their children for philosophical reasons?
Yes ……………………… 56
No ………………………. 33
Don’t Know/Other Response ….. 11

There are still outbreaks of vaccine-preventable diseases like measles and mumps in this country. Unvaccinated children are eight times more likely to get measles than those who’ve gotten the full series of shots. About 77 percent of children have received all recommended shots by the time they are three years old. Is this a very serious public health concern, or not.

Very Serious Concern ………. 66
Not Very Serious Concern …… 26
Don’t Know/Other Response …… 8

Would you recommend that all children in your family get all recommended vaccinations, or would you want your family to ask lots of questions before proceeding with vaccinations?
Get all vaccinations ………. 56
Ask Lots of Questions First … 38
Don’t Know/Other Response …… 6
(Distributed by Scripps Howard News Service, http://www.scrippsnews.com)

Thimerisol Is Just Another Word for Toxic

Wednesday, September 3rd, 2008

Mary Tocco wrote a well reasoned and articulate summation of the dangers of thimerisol, which is 50% mercury by weight, in vaccinations. This article should be shared with anyone, whether a doctor, parent, school official or public health official, who thinks that it might be good public policy to vaccinate anyone, including children.
When they have digested this information, please let them know that the other components of vaccines, including stray DNA from aborted fetuses and animals, genetically modified DNA, aluminum, squalene, formaldehyde, polysorbagte 80 (a known cause of infertility), FDA-acknowledged “steal viruses”, including some that cause leukemia and other cancers and a witches’ brew of other poisons are regularly introduced into humans despite the irationality of doing so from a health or logic point of view.
Let me know what happens!
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
www.NaturalSolutionsFoundation.org
www.Organics4U.org
www.NaturalSolutionsMedia.tv
www.NaturalSolutionsMarketPlace.org

To the Editors of Scientific American
Tue, August 26, 2008

Dear Editors,
I am continually shocked at the misinformation your magazine perpetuates about toxic vaccines. Consider the following FACTS pertaining to mercury/thimerosal:
• Manufactured by Eli Lilly in 1930 and put in vaccines and other topical agents in 1930 as a disinfectant.
• 1948 Blue Ribbon Panel appointed by Washington deemed it “very toxic” and ordered it removed from all topical and biological. They removed all topical applications and supposed to remove all biological with mercury. Dr. Frank Engly, only living member of that panel. Their recommendations were ignored due to “POLITICS”.
• 1956 – CD gets reports on the toxicity of thimerosal, removed murcuralate, mecurocome and other topical applications.
• Thimerosal is toxic and accumulates in the brain. (Dr. Boyd Haley, University of Kentucky, mercury specialist)
• Department of Defense during WW2 said Eli Lilly must label it “POISON”
• 1971 Eli Lilly’s own study said it was “Toxic to tissue cells in concentrations as low as one part per million”.
• That is 100 times weaker than what has been given to babies for the last 20 years.
• 1997 10 babies died when thimerosal was dabbed on their umbilical cord after birth, Toronto, Canada
• Russia banned thimerosal in vaccines 20 years ago as did Denmark, Great Brittan and all Scandinavian countries.
• Prior to 1999- 2003 Congressional Hearings, doctors did not know the level of thimerosal in vaccines and any doctor in their right mind would NEVER say that mercury in any form is safe at any level.
• Children got between 40 to 60 times the EPA safety level injected with vaccines. (Dept. of Biologic, Evaluation and Research, 2003 Congressional hearings.)
• It took until late 2003 to use up all the vaccines containing the full dose of mercury, they were never recalled and Con. Dan Burton said in 2000, “Every day these vaccines are given, 8000 children are at risk”. Over the next 3 1/2 years over 11 million children were at risk from those vaccines.
• When mercury/thimerosal is combined with Aluminum, the two act synergistically and drive the mercury deeper into the brain tissue. (Dr. Boyd Haley)
• Mercury is absorbed into fatty tissue very quickly…that is why is it not in the blood for long. To say that it is eliminated quickly is a total outright lie. Autistic children suffer with toxic metal injury from mercury and aluminum. It is not found in the blood after a few days because it has been absorbed by the fatty tissue including the brain. When you challenge the body to “dump the toxic metals”, their tests are off the charts!!! A blood test will not show that.
Having given you some of the FACTS on mercury keep in mind this does not even consider other toxic ingredients found in all vaccines: Aluminum, Formaldehyde, Alum, Acetone, MSG, Glycerin, foreign viruses from growth mediums, much more all listed on http://www.novaccine.com/

I think that anyone who believes that vaccines are safe needs to step up, drop their britches and bend over, and get the very same vaccines they recommend for the babies, only make them WEIGHT APPROPRIATE! Then get them every 2 months for the next 2 years. A one year old baby weighing 30 pounds will get the same flu shot that a 300 pound man will get, with 25 micrograms of mercury. One doesn’t need to be a MD to see that this policy is terribly flawed… to put it mildly.

WAKE UP! We are not so easily led anymore! We want true science and not bias, junk science. Parents are smarter than you think and you just made your magazine lose credibility once again.

Mary Tocco
Private Vaccine Investigator for the last 28 years
Public Speaker
Producer of, “Are Vaccines Safe?”

Who Owns The Gene That Kills You? And Does Your Estate Have to Pay Royalties to Them?

Wednesday, September 3rd, 2008

The article quoted at the end of this post says:

“Admittedly, there is something very odd, and slightly disturbing, in the spectacle of a fight over who owns the DNA of a virus that could kill millions of people around the world. Should a country retain property rights to the strains of diseases that plague its citizens? There is also, as always, the niggling question of how the world is to fund the development of new vaccines if the few companies that are capable of producing the medicine aren’t compensated for their efforts. Finally, it would seem to me that there is a clear difference between a U.S. government agency owning a patent and a company such as GlaxoSmithKline staking the claim.”

DNA as property is a terrifying reality. When the US Supreme Court opined that genomes could be patented, the risk to the global biosphere was generally little recognized. Given the unstable and unpredictable consequences of biotechnology insertion of genes into host genomes, and the novel (and potentially harmful or lethal) molecules coded for by this process, the “ownership” of viral DNA sequences is even more ominous.

Weaponization of the avian flu has already taken place through
1. Combining the genome of “seasonal flu” viruses with the then-harmless H5N1 avian flu to find the combinations which yielded enhanced pathogenicity (NIH, 2006),
2. Reconstruction of the genome of the most successful bio weapon in history, the 1918 pandemic flu virus (NIH, Mt Sinai Med. Coll, 2000 – 2006)
3. Intentional combination of the H5N1 virus with the newly reconstructed 1918 pandemic flu genome (NIH, Mt. Sinai School of Medicine, 2006).

Vaccines allegedly protective against this novel virus are then developed and, like the Sanofi-Pasteur vaccine manufactured in China after approval in the absence of formal human trials, sold to governments for vast sums of money (e.g., 100M doses @$15 US per dose) for stock piling.
Indonesia now says that it owns its valuable resource, the supposedly deadly Avian Flu virus. The United Nations issued a special report on the thorny question of whether a virus that kills someone in a particular country “belongs” to that country.

Besides the absurdity of owning life, and creating a totally artificial geographic demarcation through which to exercise control of that organism, the impetus to commercialize pathogens for nation states and predatory companies will, I fear, prove irresistible. Now add organized crime and rogue states (large or small) into the mix and you have a recipe far, far more toxic than the supposed pandemic Avian Flu.

Greed and technology are a deadly mix. If you doubt that, look at the so called “Health Care” system in the West and consider that since it makes no money if you are well, its best interest is served by the weaponization of food (i.e., Codex Alimentarius – see my video “Nutricide” on our website, www.HealthFreedomUSA.org or www.YouTube.com/NaturalSolutions) and the demonization of natural prevention and treatment so ubiquitous in the West.

Ownership of life forms, pathogenic or otherwise is, in short, a massive error and a monstrous reality which must be reversed for everyone’s benefit.

On August 21, Andrew Leonard wrote an article called Biopiracy and Bird Flu. That article, which follows, discusses the consequences of the confluence of the US Supreme Court’s decision to allow ownership of organisms, the unbridled greed and lack of ethics of the pharmaceutical/illness care industry and the horrifying reality of the depopulation agenda which, thanks to blatant hubris and Freedom of Information Act suits, is no longer speculation but fact.

Prince Phillip yearning to “come back” as an Ebola virus so that he can help depopulate the planet and Henry Kissinger’s Memo 200, the Council on Foreign Relations documents, the Phillipine Supreme Court’s finding that WHO vaccines did, indeed, contain permanent sterility agents which sterilized some 3 million unsuspecting women (and the use of the same technology in Africa, South and Central America, South East Asia and elsewhere) followed by the tardy admission of the World Health Organization that they were using such agents mixed into vaccines are part of a patchwork of death and global supremacy which is horrifyingly plain to see, yet tragically, criminally, perhaps, overlooked by the MMD (Media of Mass Deception).

The worm, or perhaps the virus, is turning now, though. Those very countries which would first be the targets of these depopulation plans and programs (the developed world is in the plan, too – Kissinger stated that depopulation should be the US’s first foreign policy priority starting with the third world, remember) have noticed that at least short term gains, but very substantial ones, can come from controlling, weaponizing and commercializing those lethal viruses among themselves. After all, once exposed to deadly agents like dioxin, ordinary viruses can mutate into very profitable killers. The US obligingly contaminated large parts of South East Asia with dioxin and other deadly poisons.
Moreover, vaccinated birds, not outside flocks, develop avian flu through mutations since they are raised in toxic environments (the birds in their industrialized chicken coops and the viruses in their poison-rich test tubes and growth bottles) and induced to mutation by those toxic conditions.

Now nations like Indonesia, Zimbabwe, Nigeria, Viet Nam and a host of others are ready for the Big Time: ready to develop, sell or license their deadly dollar cargo to the even bigger boys: the US, WHO or Big Pharma. All of this falls apart, of course, if the Bigger Boys get their hands and microscopes and vats on these “resources” first.

As events would have it, the fears that they will be done out of their valuable resources is quite accurate. Indonesia is not going to like the fact that a WHO affiliate, the CDC, has applied for a patent on the genome of the Indonesian Avian Flu. Nor will it be happy with the fact that GlaxoSmithKlein is manufacturing a “preventive” Avian Flu vaccine using strains from Viet Nam and elsewhere. So these fears about loosing significant revenue are not unfounded.

Do you find something wrong with this picture? The Natural Solutions Foundation certainly finds the trend, and the mindset, beyond ominous.

Let’s say you’ve got a lab, a virus and a hereditary tribe your people have been warring with for a thousand years. Like the “Islamic Nuclear Bomb” (or the Capitalist Nuclear Bomb), or Depleted Uranium or any other weapon of mass destruction, the mutated, weaponized virus in your tanks could be used on your enemies with the ever present justification that people build for themselves in situations like this. Or, if vaccines were to actually work, you could imagine giving the vaccine to your people and unleashing the disease on the other tribe.

Or, if you are the US, you could stockpile untested, not particularly safe or effective vaccines which would cause widespread… what? Illness? Death? Cancer? Infertility? Adult Autism? Novel vulnerabilities or diseases? Remember, there is no liability in the US for whatever a previously approved drug or vaccine does to you or your child or your mother or your ….

Merchants of death, indeed. Is this the world we want to leave to our children? What are you ready to do about it?

Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
www.NaturalSolutionsFoundation.org
www.Organics4U.org
www.NaturalSolutionsMedia.tv
www.NaturalSolutionsMarketPlace.org

Become a supporter. Make a regular, recurring tax deductible donation here (http://www.healthfreedomusa.org/index.php?page_id=189) or contact Ralph Fucetola, J. D., ralph.fucetola@usa.net, to learn how to make other types of tax deductible gifts to the Natural Solutions Foundation.

Now, here is the Salon.com article referred to above:
In late 2006, Indonesia sparked a furor in the international public health community when the country announced it would no longer supply samples of the H5N1 strain of bird flu to the World Health Organization. It wasn’t fair, complained the developing nation, which is second only to Vietnam in recorded cases of human deaths from bird flu: Indonesia was providing crucial data for researchers working on vaccines, but prices for proprietary pharmaceutical products resulting from that data were too high for most Indonesians to afford. If you want to understand why citizens of developing nations get aggrieved about biopiracy, there’s a clue.

After a flurry of worldwide publicity, Indonesia relented, and in March announced it would resume sending samples to the W.H.O., provided that the samples were not made available to commercial organizations. The debate over how best to serve the interests of both developing nations and pharmaceutical companies was by no means resolved, and according to the New York Times, Indonesia received only a tepid promise from W.H.O. “not to pass their samples on to commercial manufacturers without consulting the health minister of the country that provided the sample,” but a clear point had been made.

Now in what appears to be something of a scoop, a freelancer writer and specialist in patents has revealed that even as Indonesia was threatening to withhold its samples, the United States government was applying for an international patent on a new vaccine that incorporates genetic code derived from Indonesian avian influenza samples.

Writes Edward Hammond, in the Aug. 15 issues of SUNS:

In a development that is likely to raise more pressing questions about reform of the WHO Global Influenza Surveillance Network (GISN), an international patent application has surfaced in which the U.S. Centers for Disease Control (CDC) and U.S. National Institutes of Health claim ownership of Indonesian influenza genes.

A recent patent search has revealed that the CDC, which is a WHO collaborating centre, is applying for a patent for a new vaccine against influenza, particularly for bird flu (H5N1). The vaccine incorporates genes from a H5N1 strain isolated from an Indonesian human victim of bird flu in 2005.

The strain that contains the genes was transferred to the WHO GISN by Indonesia for characterization for public health purposes, but may wind up as the property of the US government.

Under U.S. law, the U.S. government agencies would offer licenses to the technology to pharmaceutical companies. The patent application indicates that the US government intends to pursue the claim in most countries of the world, including Indonesia itself, as well as neighboring countries.

One follower of intellectual property and public health at the blog IPMed found the patent application “troubling”:

The patent application raises specific questions about the US CDC, which is a WHO Collaborating Center for influenza virus studies. The WHO Collaborating Centers receive influenza viruses from donor countries for public health characterization purposes, and not for the purposes of making proprietary claims. The Global Influenza Surveillance Network’s effectiveness rests on the prompt sharing of and access to viruses from all donors. However, one wonders how many donor countries will wish to continue to share influenza viruses for research and vaccine development if it is that Governments who operate Collaborating Centers are minded to make proprietary claims over the materials which they have received as a result of the GISN system. Obviously this patent application built on the back of the GISN system of virus sharing will call into question the entire system and may very well undermine its effectiveness.

Admittedly, there is something very odd, and slightly disturbing, in the spectacle of a fight over who owns the DNA of a virus that could kill millions of people around the world. Should a country retain property rights to the strains of diseases that plague its citizens? There is also, as always, the niggling question of how the world is to fund the development of new vaccines if the few companies that are capable of producing the medicine aren’t compensated for their efforts. Finally, it would seem to me that there is a clear difference between a U.S. government agency owning a patent and a company such as GlaxoSmithKline staking the claim.

Unless, of course, the U.S. does end up licensing its patent to Big Pharma without requiring some developing nation equity, in return.

http://www.salon.com/tech/htww/2008/08/21/biopiracy_and_bird_flu/index.htm
http://darwiniana.com/blogzone/2008/08/31/who-owns-the-bird-flu-virus/#comment-251

Wellcome Trust Funding Examination of Why H5N1 Virus Isn’t Pandemic Yet!

Wednesday, September 3rd, 2008

The Pharmaceutical Cartel is concerned… people are not dying to take their latest concoction: a “pre-pandemic” vaccine!

In an extraordinary announcement, the Wellcome Trust, is providing funding to find out why the H5N1 Virus, widely advertised as the organism that would create the mother of all pandemics, has so far failed to live up to its billing.

Before looking at the remarkable interest which this Trust has supporting this study, we should know a bit about the Wellcome Foundation. A quick visit to its web site, http://www.wellcome.ac.uk, tells us a heart warming story:

In 1880, two young Americans – Silas Mainville Burroughs and Henry Wellcome – established a pharmaceutical company, Burroughs Wellcome & Co. In 1895, Silas Burroughs died, leaving the company in the hands of his partner. The firm flourished under Wellcome’s leadership.

Henry Wellcome set up several research laboratories loosely linked to the drugs company – a highly original step at the time – and employed some of the most outstanding scientists of the day. He also indulged his passion for collecting artefacts related to medicine.

In 1924, Henry Wellcome consolidated all his commercial and non-commercial activities under one corporate umbrella: The Wellcome Foundation Limited. He died in 1936, at which time the Wellcome Trust was established.

In his will, Wellcome vested the entire share capital of the drug company, The Wellcome Foundation Limited, in individual Trustees. The Trustees were charged with spending the income according to Sir Henry’s wishes.

http://www.wellcome.ac.uk/About-us/History/index.htm

We also learn that “The Wellcome Trust remained the sole shareholder of The Wellcome Foundation Limited until 1986. In that year, the Foundation became a public limited company, Wellcome plc, and was floated on the London stock market. The company merged with Glaxo plc in 1995, to form a new company, Glaxo Wellcome plc, and merged again with SmithKline Beecham plc in 2000 to form GlaxoSmithKline. “http://www.wellcome.ac.uk/About-us/History/Wellcome-business/index.htm

A look at GlaxoSmithKline tells us that in July, 2006 it announced in a Washington Post article that a new version of a vaccine against a strain of H5N1 virus that killed people in Viet Nam in 2004 was worthless without a new, secret adjuvant but people developed antibodies to very low doses of the vaccine with the adjuvant. Adjuvants are immune irritants like aluminum (associated with Alzheimer’s Disease), sqalene (associated with lethal auto immune responses) and other highly toxic substances. No mention is made of safety or safety testing for this secret adjuvant in the article.

The same article goes on to say that authorities generally require 70% of a population to develop antibodies to a vaccine if it is to be accepted as “safe and effective” medicine for us (throwing the entire “theory” of “herd immunity” into a very cocked hat, indeed, by the way). The same article also mentions, very close to the bottom, that it is not at all certain the vaccine against the 2004 Viet Nam H5N1 strain would confer immunity or protection in the event of an avian flu pandemic contagion, noting, “A key unanswered question is whether the antibodies against that strain would protect a person against other strains.” http://www.washingtonpost.com/wp-dyn/content/article/2006/07/26/AR2006072601716.html

On May 19, 2008, Medical News Today noted that “Many experts believe it is only a matter of time before the deadly H5N1 bird flu virus, which currently humans can only catch from infected birds, mutates into a form that spreads easily from human to human and when it does so it will kill millions of people all over the world.” and enthused that “Global pharmaceutical company GlaxoSmithKline (GSK) is the first to get the go ahead for a wide spectrum vaccine to protect humans ahead of a possible future bird flu pandemic now that the European Commission (EC) is giving the drug giant approval today, Monday, to market its pre-pandemic vaccine Prepandrix in all 27 member states of the European Union (EU), according to various media reports.”

The same article notes, ” Chief executive of GSK, Jean-Pierre Garnier said that:

‘This vaccine marks a significant step in the world’s ability to cope with an influenza pandemic.”

“It is testament to GSK scientists who have pioneered the approach to pre-pandemic vaccination, demonstrating our commitment to doing everything we can to help prevent the devastating effects of a pandemic,” he added.

Although Prepandrix has only just received its first regulatory approval, countries such as the US, Switzerland and Finland have already started stockpiling the vaccine, sales of which last year topped 200 million US dollars (102 million GB pounds). GSK said stockpiling means countries will be able to deal with an outbreak sooner rather than waiting for a vaccine to be developed for a particular strain….

“This drug represents one of the swing factors affecting us in 2008.” http://www.medicalnewstoday.com/articles/107910.php

This means, of course, that the US is already stockpiling a vaccine which it has neither tested nor approved. A vaccine created on a premise which is totally untried and tested: that a vaccine against something that killed somebody will provide protection for somebody else if they encounter another type of pathogenic (disease causing) organism. It’s an interesting, and apparently highly profitable theory, but does it have much to do with reality? And just how safe is this vaccine with the super secret adjuvant? [Using an untested drug is treated as a crime in the US. How has this law been circumvented? REL]

Next it is instructive to note that, having already made a great deal of money on a unvetted vaccine based on an untested premise from the US and other countries where it has not been approved, the ever ethical GlaxoSmithKlein announced at ClinicalTrails.Gov a US clinical trial in adults for a vaccine already being stockpiled in the US:

July 2008

Sponsors and Collaborators: GlaxoSmithKline [and] Department of Health and Human Services
Information provided by: GlaxoSmithKline
ClinicalTrials.gov Identifier: NCT00719043
Purpose: The purpose of this study is to determine whether [emphasis added – REL] GSK’s avian flu vaccine GSK 1557484A is immunogenic [that is, does it produce an immune response, not whether it is safe or works – REL] when given to adults aged >=18 years.

http://clinicaltrials.gov/ct2/show/NCT00719043

Before we go on, we should recall that Avian Flu vaccines are rich plums and are pretty low hanging as well: the vaccines do not have to be particularly safe or effective, just profitable. Very profitable, with Congress providing the “insurance” against vaccine induced injury (supported by a special vaccine tax vaccine “consumers” are forced to pay) that guarantees these endless profits.

The standards for vaccines are bargain basement science: some sort of immunological response has to be produced, but the person does not necessarily wind up being “protected” (which is why most epidemics occur in totally or nearly totally vaccinated populations) and safety is assessed so lightly and so poorly that, in the context of guaranteed immunity from any prosecution or liability findings in any court in the US, vaccine companies have little trouble picking those fruits. See, for example,

GlaxoSmithKline, Novartis and Iomi Land Avian Flu Vaccine Contracts
January 17, 2007 · Filed Under General

by H.S. Ayoub
BioHealth Investor.com

The Department of Health and Human Services (DHHS) has awarded GlaxoSmithKline (GSK), Novartis Vaccines and Diagnostics (NVS) and Iomi (IOMI) all a total of $133 million in funding for the development of H5N1 Avain Flu vaccines.

GSK’s contract will total $63 million over 5 years, while Novartis will receive $55 million over the same period.

http://www.biohealthinvestor.com/2007/01/glaxosmithkline-novartis-and-iomi-land-avian-flu-vaccine-contracts.html

Now on to the search for the Perfect Pandemic storm: Here is the press release provided a few days ago to hail the generous funding of the Wellcome Trust to help scientists figure out what is taking the pandemic H5N1 flu so long to get started. Considering that in 2006 the US Government is reported to have mailed unprotected, unmarked vials of the newly reconstituted Pandemic 1918 flu virus to labs and hospitals all over the world (was that genome inserted in an H5N1 strain of Avian Flu or not? – the Natural Solutions Foundation does not yet have that information but would greatly appreciate knowing whether it was; we know people from government sites read this blog… won’t one of you become a whistle blower and save the lives of millions?). The media reports that several people are reported to have died from various strains of H5N1. It is remarkable, indeed, that after all that research, and all that hype, there is no H5N1, or H7N1 or any other Avian Flu Pandemic – YET.

Does the Welcome Trust aim to do something about that?

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“Scientists examine bird flu infections to monitor for ‘pandemic’ mutations”

Scientists funded by the Wellcome Trust are to examine what is preventing the H5N1 avian influenza virus from causing a human pandemic and what mutations are required to realise its deadly potential. The research could hold the key to early identification of a potential influenza pandemic, and to developing drugs and a vaccine.

Since its reappearance in 1997, the H5N1 influenza virus has caused disease and death in millions of birds around the globe. The number of infections in humans is still relatively small, however: from 2003 to the end of June 2008 there had been 385 known cases in humans, 243 of them fatal(1). So far, there appear to have been very few cases of human-to-human transmission.

Professor Ten Feizi at Imperial College London believes one reason why H5N1 has not yet evolved into an effective pathogen capable of widespread transmission between humans lies in how the virus attaches itself to the respiratory tract. She is leading an international research project which has received over £720,000 from the Wellcome Trust to identify the receptor molecules in the human respiratory tract to which viruses attach and to look at how changes in the binding protein on the surface of the virus might increase its ability to attach to the tract and cause infection.

Professor Feizi will work with Professors Menno de Jong and Jeremy Farrar from the Wellcome Trust’s South East Asia Programme in Vietnam, Dr Alan Hay and Dr Steve Gamblin at the Medical Research Council National Institute for Medical Research, London, and Dr Mikhail Matrosovich at the Philipps University of Marburg, Germany.

“Over the last few years particularly in Asia we have seen just how deadly the H5N1 virus can be,” says Professor Farrar from the Oxford University Clinical Research Unit in Ho Chi Minh City, Vietnam, where a number of people have been treated for infection by the virus. “So far, we have been relatively fortunate and there has been only limited evidence of the virus transmitting from human to human. The more we understand about the virus, how it interacts with the body, the better we will be prepared for any serious mutations that may arise.”

In humans, influenza infection occurs via the respiratory tract, or airway. In order to cause disease, the virus must enter the body’s cells where it can replicate and spread, but it must first find a site to which it can attach, known as a receptor. The virus can only attach to and enter the cells if the receptor fits into the binding proteins, or haemagglutinins (the “H” in H5N1), on the surface of the virus.

Previous research has shown that the haemagglutinin on H5N1 favours a particular form of receptor known as a “2,3 receptor”. These are abundant on cells of birds, but in humans are found mostly on cells of the lower respiratory tract (the lungs). Professor Feizi and colleagues have shown that mucus in the upper airway in humans also contains 2,3 receptors, but here the mucus acts as a defence mechanism to which the virus binds, blocking its progress and enabling the body to “sweep out” the virus. Both factors suggest that huge doses of the virus are required in order to infect humans, a theory supported by evidence that those who have become infected have spent large amounts of time in close proximity to infected fowl.

As with all viruses, H5N1 is continually mutating, and it is changes that allow the virus to attach to “2,6 receptors” in the human upper airway which may enable the virus to become more infectious to humans.

“If the bird flu virus evolves to favour the receptors in our nose and throat like normal flu, the results could be devastating,” says Professor Feizi from the Division of Medicine at Imperial College London. “We could have a virus which is not only highly infectious but is easily transmissible by coughing and sneezing.”

Dr Hay and Dr Gamblin will isolate haemagglutinin from samples of the virus taken from the patients in Vietnam, and Dr Matrosovich will grow cultures of human airway cells and isolate cell-membrane receptors and secreted mucus. Then, using a technique known as neoglycolipid (NGL) microarray analysis developed by Professor Feizi and her colleagues, the team at Imperial College will identify which of the various receptor structures the haemagglutinins bind most strongly to. Dr Gamblin’s team will then use X-ray crystallography to probe, at the molecular level, how mutations might cause the bird virus to change into a human virus.

“If we can find out which mutations of haemagglutinin prefer which receptors, we may be able to identify quickly or even predict which mutations give the virus pandemic potential,” says Professor Feizi.

Current antiviral treatments for influenza, such as Tamiflu, target neuraminidase (the “N” in H5N1), which is responsible for allowing the virus to jump off receptors on one cell and bind to those on another cell, and to replicate and spread once inside the body.

“Targeting the virus’s ability to bind to the receptors – which until now has proved far more difficult – may provide an alternative, more effective way of preventing infection,” says Professor Feizi. “We hope that our work will make this process simpler and faster.”

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1. Cumulative Number of Confirmed Human Cases of Avian Influenza A/(H5N1) Reported to WHO, 19 June 2008. http://www.who.int/csr/disease/avian_influenza/country/cases_table_2008_06_19/en/index.html

http://www.eurekalert.org/pub_releases/2008-08/wt-seb082908.php

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Here is my question to you, dear reader: Are you convinced by the tag line which comprises the very last paragraph of this press release? Or, given the financial investment of the drug companies in having, not preventing, a pandemic, would you put your money on the “Where did that super Pandemic get to? By George, let’s go find it!” horse?

Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
www.NaturalSolutionsFoundation.org
www.Organics4U.org
www.NaturalSolutionsMedia.tv
www.NaturalSolutionsMarketPlace.org

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