The Chemical Castration of our Children’s Brains

Common Sense Show
by Dave Hodges

Government should not be in the business of mandating personal choices and government should never be allowed to legislate choices which should be reserved for parents with regard to their children’s health and welfare. The parents are sovereign over the welfare of their children, not the state.

In the name of increasing the corporate bottom line, the government watchdog industries of the DEA and FDA, as well as the office of the President, have become the willing lap dogs for Big Pharma and this unholy alliance is serving to endanger our children.

Big Pharma has gone to great lengths to increase sales to the youth of America either through chemically castrating our children’s brains or by producing drugs with very serious side effects which serve to seriously degrade both the brain and the body. Our children are being systematically destroyed by the pharmaceutical industry.

The Ritalin Conspiracy

Let’s make up a brain disorder, which parallels normal restlessness of children and then transform a dangerous drug, methamphetamine, and get as many kids on the drug as possible. It is good work if you can find it and pharmaceutical companies like Merck and Eli Lilly are leading the way in medical fraud and in the name of record corporate profits

The use of Ritalin has become so rampant, that even the DEA has become alarmed by the tremendous increase in the prescribing of these drugs in recent years. Since 1990, prescriptions for methylphenidate have increased by 500%, while prescriptions for amphetamine for the same purpose have increased 400%. The American Pediatric Association claims Ritalin is over prescribed by 600%.

For well over a decade, many scientists have speculated that ADD drugs are dangerous and can cause serious injury and death. Etta Brown, a licensed educational psychologist and author of Learning Disabilities: Understanding the Problem and Managing the Challenges explained in response to her study that drugs like Ritalin actually destroy the neural function in children’s brains. As a result, children who have undergone treatment with Ritalin will actually have a much more difficult time processing information and learning new things. This kind of defeats the purpose of getting children to sit still in school while placed in a zombified state.

Brown further reported that Ritalin is responsible for the development of a permanent tic in the face, neck, and head of many of the children who have taken or are taking it. Ironically, Ritalin is responsible for causing far more serious neurological damage than the problems it is alleged to treat. Meta analyses studies over the years have revealed that while drugs like Ritalin visibly place children into a trance like state, these drugs destroy the vulnerable, delicate and developing nervous systems which can and does permanently cripple their ability to function as normal human beings.

The Gardasil Conspiracy

Last year a bill sponsored by Toni G. Atkins, D-San Diego passed into California state law which places every child in danger in California. Atkins bill begs the question of who has the ultimate authority of the welfare of our children. Is it the state or is it the parents? Well, if you live in California, the nanny state purports to have the final say. The Atkins bill makes it legal for a school district or a doctor to medicate or inoculate a child without parental notification.

In an era when Gardasil has resulted in needless tragedy for over 40,000 children who have been vaccinated by well intentioned doctors who are ignorant of the side effects, we are now witnessing states like California mandating the forced inoculation of young girls with Gardasil.

What the medical establishment is not telling you is that thousands of girls are having adverse reactions to the HPV Vaccines, some have even died -at last count, at least 103 lives have been lost to Gardasil. This is a brilliant strategy being invoked by California. Let’s kill the girls, thus preventing them from having sex, thus, preventing STD’s.

You remember MERCK don’t you? They were the creator of the wonder death drug, Vioxx. This is the same Merck, who only after intense pressure from the medical community and the media decided to pull the dangerous drug, Vioxx, from the market after an estimated 140,000 adverse reactions had already occurred. And the pulling of Vioxx occurred only after a safety trial was stopped because there was an undeniable and increased risk for serious cardiovascular dangers such as heart attacks and strokes from using the drug.

Merck has been no less reckless in their administration of Gardasil as they were with Vioxx. First and foremost, Merck and the Food and Drug Administration’s clinical trials have been called into question for blatant fraud committed during the required FDA testing period. Both the control group and the experimental group, in the clinical trials, were given the aluminum adjuvant contained in the Gardasil. Control group and experimental group comparisons are done to ensure public safety from adverse side effects as much as possible. In this case, it would have be standard practice to provide the control group with a saline solution instead of the aluminum adjuvant in order to determine the risk posed by the adjuvant given to the experimental group. In failing to follow these research norms, Merck and the FDA have endangered the public health.

These research protocols violate every known tenant to proper research; it represents an air of unprofessionalism, not to mention criminal fraud, which clearly demonstrates collusion to commit fraud against the general public on behalf of Merck as sponsored by the FDA. In fact, Judicial Watch was forced to file a lawsuit under the Public Records Act in order to obtain the obfuscated side effect results as the FDA tried to cover up their own complicity in this research fraud by refusing to release the relevant documents.

Gardasil is marketed as a vaccine that prevents cancer, but the drug has not been evaluated for the potential to cause cancer or genotoxicity. Gardasil is a prophylactic, preventative vaccine and is of absolutely no value in the treatment of a pre-existing HPV infection. It is neither a cancer vaccine nor a cure; yet, the public has been led to believe that this is the case. The New England Journal of Medicine found that there remains no conclusive proof that Gardasil altered the course of HPV-16 or HPV-18 infection for which the patient was symptomatic prior to the administration of the first dose. In other words, this is fraud in the first degree.

Gardasil is the most costly vaccine ever to be approved by the FDA. However, its long-term effectiveness is not known and several estimates state that Gardasil’s life as a vaccine could be only two to three years. This opens up the distinct possibility that a Gardasil vaccinated child will require several booster shots which will undoubtedly increase the bottom line for Merck, but the risk for side-effects among the vaccinated could increase exponentially with each successive vaccination.

The VAERS reports show that as many as eighteen people have died after receiving Gardasil. The VAERS reports document identifies 38 reports of Guillain-Barre Syndrome among juvenile females who previously received the Gardasil vaccine. Guillain-Barre Syndrome is a catastrophic illness that attacks the nervous system which can and often does result in paralysis. Ironically, Gardasil is being developed against only four types of HPV. However, there is over 100 strains of HPV, 30 of which are transmitted sexually. Just what could have Governor Brown and Atkins been thinking?

Do you not think that this is the first time that this kind of dangerous medical fraud has been and will be visited upon your children for profit and political career advancement? Think again! The American Academy of Pediatrics recommends that boys of the age of 11 to 12 years should be vaccinated with the vaccine against HPV with the Gardasil vaccination.

Even my doctors are serving the Big Pharma agenda, as evidenced by the fact that my son’s former pediatrician relentlessly tried to give my then 11 year old son the Gardasil injection. When I presented the good doctor with some of the data contained in this report, he replied “your ideas are not contained within the mainstream of medicine.” Since when is scientific research required to reflect the mainstream of the Big Pharma agenda? The moral of this story is to fire your doctor and find a health care provider who is committed to the welfare of their patients.

CEO Who Oversaw Mass Vioxx Deaths Now Teaching at Harvard and on Microsoft Board of Directors

AllGov

Raymond Gilmartin’s landing was a soft one after leaving behind an embattled Merck. The one-time top executive of the leading pharmaceutical company, which was engulfed in the Vioxx controversy last decade, splits his time these days between teaching part-time at Harvard and serving on the boards of major corporations.

Gilmartin served as Merck’s president and CEO for 12 years (1994-2006) during troubles that stemmed from the company’s anti-arthritis medicine Vioxx. Despite knowing that Vioxx was potentially lethal, Merck put it on the market in 1999. Although a Food and Drug Administration study showed that perhaps 55,000 Americans died from heart attacks and strokes after using Vioxx, other sources indicated that upwards of 500,000 people—almost all of them older adults—may have died from the drug, which produced lawsuit after lawsuit against Merck. The company wound up settling for $4.85 billion.

Before it was pulled from the market in 2004, the drug was very profitable for Merck, earning about $2 billion per year in revenue at its peak. It also paid handsomely for Gilmartin, who reportedly made $50 million in just five of his years at the corporate helm.

After retiring from his post, Gilmartin joined the faculty of Harvard Business School, where, according to the school’s Web site, he still serves as an adjunct professor, teaching second-year MBA candidates to run businesses just like he did in a course called Building and Sustaining Successful Enterprises.

Gilmartin also serves on the boards of General Mills, Inc., and the Microsoft Corporation.

When Half a Million Americans Died and Nobody Noticed

OpEdNews

Was the US drug Vioxx responsible for far more deaths than has been acknowledged so far?

RE American lives cheaper than those of the Chinese? It’s a question raised by Ron Unz, publisher of The American Conservative, who has produced a compelling comparison between the way the Chinese dealt with one of their drug scandals – melamine in baby formula – and how the US handled the Vioxx aspirin-substitute disaster.

The Chinese scandal surfaced in 2008, shortly before the Beijing Olympics. Crooked dairymen diluted their milk products, then added a plastic chemical compound called melamine to raise the apparent protein content back to normal levels. Nearly 300,000 babies across China suffered urinary problems, with many hundreds requiring lengthy hospitalisation for kidney stones. Six died.

Long prison sentences were handed down and a couple of the guiltiest culprits were tried and executed for their role. Throughout these events, American media coverage was extensive, with appropriate sneering about the Chinese leadership’s indifference to human life.

Four years earlier, in September 2004, Merck, one of America’s largest pharmaceutical companies, issued a sudden recall of Vioxx, its anti-pain medication widely used to treat arthritis-related ailments.

The recall came just days after Merck discovered that a top medical journal was about to publish a study by an FDA (Food and Drug Administration) investigator indicating that the drug in question greatly increased the risk of fatal heart attacks and strokes and had probably been responsible for at least 55,000 American deaths during the five years it had been on the market.

It soon turned out Merck had known of potential lethal side effects even before launching Vioxx in 1999, but had brushed all such disturbing tests under the rug.

With a TV ad budget averaging a hundred million dollars per year, Vioxx swiftly became one of Merck’s bestsellers, generating over $2 billion in yearly revenue. Twenty-five million Americans were eventually prescribed Vioxx as an aspirin-substitute thought to produce fewer complications.

There was a fair amount of news coverage after the recall, but pretty slim considering the alleged 55,000 death toll. A class-action lawsuit dragged its way through the courts for years, eventually being settled for $4.85 billion in 2007.

When the scandal first broke, Merck’s stock price collapsed, and many believed that the company could not possibly survive, especially after evidence of a deliberate corporate conspiracy surfaced. Instead, Merck’s stock price eventually reached new heights in 2008 and today it is just 15 per cent below where it stood before the disaster.

The year after the scandal unfolded, Merck’s long-time CEO resigned and was replaced by one of his top lieutenants. But he retained the $50 million in financial compensation he had received over the previous five years. Neither he nor any other Merck executives was charged with corporate malfeasance.

Senior FDA officials apologised for their lack of effective oversight and promised to do better in the future. The Vioxx scandal began to sink into the vast marsh of semi-forgotten international pharmaceutical scandals.

Then in 2005, as he now remembers it, Ron Unz “was reading my morning newspapers, as I always do, and noticed tiny items about an unprecedented drop in the American death rate. Hmm I said, I wonder if that might have anything to do with all those other stories about that deadly drug recently taken off the market and all the resulting lawsuits.”

The year after Vioxx was pulled from the market, the New York Times and other media outlets were running minor news items, usually down-column, noting that American death rates had undergone a striking and completely unexpected decline. These were what Unz, a dedicated news browser, was reading.

Typical was the headline on a short article that ran in the 19 April 2005 edition of USA Today: ‘USA Records Largest Drop in Annual Deaths in at Least 60 Years.’ During that one year, American deaths fell by 50,000 despite the growth in both the size and the age of the nation’s population. Government health experts were quoted as being greatly “surprised” and “scratching [their] heads” over this strange anomaly, which was led by a sharp drop in fatal heart attacks.

For his Chinese melamine/Vioxx comparison, Unz went back to those 2005 stories. Quick scrutiny of the most recent 15 years worth of national mortality data provided on the US Government’s Centers for Disease Control and Prevention website offered Unz some useful clues.

“We find the largest rise in American mortality rates occurred in 1999, the year Vioxx was introduced, while the largest drop occurred in 2004, the year it was withdrawn,” says Unz. “Vioxx was almost entirely marketed to the elderly, and these substantial changes in the national death-rate were completely concentrated within the 65-plus population.

“The FDA studies had proven that use of Vioxx led to deaths from cardiovascular diseases such as heart attacks and strokes, and these were exactly the factors driving the changes in national mortality rates.”

The impact of these shifts, Unz points out, was not small. After a decade of remaining roughly constant, the overall American death rate began a substantial decline in 2004, soon falling by approximately five per cent, despite the continued ageing of the population. This drop corresponds to roughly 100,000 fewer deaths per year. The age-adjusted decline in death rates was considerably greater.

“Patterns of cause and effect cannot easily be proven,” Unz continues. “But if we hypothesise a direct connection between the recall of a class of very popular drugs proven to cause fatal heart attacks and other deadly illnesses with an immediate drop in the national rate of fatal heart attacks and other deadly illnesses, then the statistical implications are quite serious.”

Unz makes the point that the users of Vioxx were almost all elderly, and it was not possible to determine whether a particular victim’s heart attack had been caused by Vioxx or other factors. But he concludes: “Perhaps 500,000 or more premature American deaths may have resulted from Vioxx [my italics], a figure substantially larger than the 3,468 deaths of named individuals acknowledged by Merck during the settlement of its lawsuit. And almost no one among our political or media elites seems to know or care about this possibility.”

I remarked to Unz that it seemed truly incredible that a greater than expected death rate of this dimension should scarcely have caused a ripple.

“I’m just as astonished,” he said. “From 2004 onwards, huge numbers of America’s toughest trial lawyers were suing Merck for billions based on Vioxx casualties – didn’t they notice the dramatic drop in the national death rate?

“The inescapable conclusion is that in today’s world and in the opinion of our own media, American lives are quite cheap, unlike those in China.

“Besides,” says Unz laughing, “it shows the stupidity of our political leaders that they didn’t seize upon this great opportunity. They should have just renamed Vioxx the ‘Save Social Security Drug,’ and distributed it free in very large doses to everyone, starting on their 65th birthday. Maybe they should have even made it mandatory, three times per day. At sufficiently large levels of national consumption, Vioxx could have almost singlehandedly eliminated all our serious budget deficit problems. ‘Vioxx – The Miracle Anti-Deficit Drug’.”