The Devastating Truth About the Obama Health Plan


Jon Rappoport
Insoultions
November 29, 2009

We are at a defining and crucial moment in our history. A machine is in motion that will alter our future. If after you read this article, you agree with its main points, or at least feel they need to be heard, send it on to others. Find ways to make your voice count.

Under the Obama Plan, it will be very convenient to declare new pandemics every few seasons.

It is one thing to read and understand the details of the Obama Health Plan. It is another thing to grasp the kind of power this bill will create, and what that power, in the future, will mean and do.

I realize that many people reading this essay have no interest in alternative medicine. However, that field represents freedom of choice for millions of Americans, and if you want to deny that choice—because you have a mistaken notion about, and a misplaced faith in, how medical science actually operates—the medical facts I describe and cite below should bring about a new appreciation of what freedom looks like, and how important the job of protecting it is.

This might be the most important medical article I’ve ever written, and in 20 years as a reporter, I’ve written many.

As I begin this essay on Thanksgiving morning, I recall that, 15 years ago, I was preparing to challenge Henry Waxman for his seat in the US House, in the 29th District, Los Angeles. At that time, the issue was Health Freedom, the right of every American to choose how to maintain and improve his/her health. And here I am again, with the same issue—only this time, there is a gargantuan White House program in place to destroy that freedom from the top down.

And various alternative-health advocates, having lost their minds, are supporting it. Among them are people who actually believe the small affirmative nods from politicians, in the direction of alternative medicine, are signaling an enlightened age under the Obama Star.

Duped again. One more time.

I have never imagined Democrats or Republicans represented the American people. This time, it is the political Left, with their naïve belief in “science” and “humanitarian work” who are leading the country over a cliff.

In the same way climate-change researchers have recently been exposed as charlatans, manipulators, and elitists, the medical establishment has been laid open and flayed—only the revelations came nine years ago. And of course, the major media refused to chase down that story and shine a light on the criminals.

On July 26, 2000, the Journal of the American Medical Association published a landmark paper by Barbara Starfield (Johns Hopkins School of Public Health), “Is US health really the best in the world?” In it, Starfield revealed what many people inside the medical establishment already knew: every year, like clockwork, the medical system was killing huge numbers of people. This wasn’t a dream. It was too real. By all rights (but who cares about rights?) the game was up. The liars and the PR flacks and the public health agencies were going down. The drug companies were going to take a lethal blow. Hospitals all over America were going to have to confess their many sins. Of course, that never happened.

Each year in the US there are:

12,000 deaths from unnecessary surgeries;

7,000 deaths from medication errors in hospitals;

20,000 deaths from other errors in hospitals;

80,000 deaths from infections acquired in hospitals;

106,000 deaths from FDA-approved correctly prescribed medicines.

The total of medically-caused deaths in the US every year is 225,000.

This makes the medical system the third leading cause of death in America, behind heart disease and cancer.

In the wake of Starfield’s devastating report, other facts came to light: 2.1 million people in America, every year, are hospitalized as a result of reactions to FDA-approved medicines. Annually, 36 million serious adverse reactions to those drugs occur.

So, inclusive health coverage for many more Americans under the Obama Plan—with business as usual—means these horrendous figures will rise.

This is the dirty secret. This is what the political Left in this country, those avid defenders of “medical science,” must pretend isn’t there at all. And the Republicans are in the same position.

Obama and his allies are promoting a medical system that is the third leading cause of death in America. It’s that stark and it’s that simple.

This is where we begin, if we are to understand the Obama Plan.

The Plan involves appointing an “expert panel” to decide what treatments Americans should be given for what diseases, under the new regime.

Only a certified idiot would assume that, over time, alternative non-mainstream therapies would survive such an ongoing vetting. Hope may spring eternal, but common sense makes it easy to grasp the realities on the ground.

Alternative therapies will die out. They will be edged out. Those that remain will be permitted for a narrow range of conditions, or as adjuncts to standard drug treatments and surgery.

Chiropractors and acupuncturists, who are temporarily basking in the notion that Obama “really cares,” are in for a very rude awakening down the line. Their careers and practices will be significantly reduced. Not today, not tomorrow, but it will happen. Perhaps these practitioners only fret about the short-term. Perhaps they’re simply looking for a few scraps from the table as long as the meal lasts.

Veteran health and medical journalist Peter Chowka points out (http://tinyurl.com/gonzalex-obama) that Americans who want to take responsibility for their own health, who don’t want onerous medical insurance, would be drafted into the Plan, and they would pay for it. With no escape possible, their discretionary incomes would shrink, and many of them would no longer be able to buy the healthiest foods and the supplements they use to prevent illness.

This is another avenue along which alternative health would approach a dead-end.

There is also the strong possibility that doctors, under the Plan, will be telling patients they may not take nutritional supplements while in treatment. This will assume the status of an irreversible edict. In certain cases, “while in treatment” means years.

What happens to a person, conscripted into the mandated Plan, who is told by his doctor that he should/must receive a vaccine? Suppose this person says no? What are the consequences? Isn’t his refusal tantamount to saying he wants out from under the Umbrella? Will he then be labeled a defector? What penalties will he suffer?

Does a diagnosis of cancer imply a patient must submit to chemotherapy, radiation, and surgery? Can these treatments be forced upon him?

Perhaps, in the early days of the Plan, nothing untoward will happen. But then, as time passes, and the system assumes tighter and tighter controls, the hand of government will close around the recalcitrant patient’s neck.

Doctors, who are an integral part of the Plan, will surely be punished if they give unapproved (alternative) treatments to patients. Their licenses will be stripped.

And in order to make the Plan operate on a day-to-day basis, the records and bookkeeping data of every health-care practitioner in America will eventually be tracked on government computer networks.

Every person in America will have a traceable medical ID package. There is no way around it. The monitoring apparatus can’t work without it.

Orwellian consequences lie up the road in the field of psychiatric practice. In case you hadn’t noticed, the invention of “disorders” by committee is the preferred method for “discovering” more and more mental illnesses. Fairy-tale figures are thrown about by the American Psychiatric Association: 20% of Americans are clinically depressed; millions of children have ADHD and need a cheap form of speed called Ritalin.

To secure the future of the Global Village, people everywhere must agree that mental illness is no longer a stigma-label. Yet, the science is completely fraudulent. For evidence, consult the many works of psychiatrist Peter Breggin, who has done more than any other person to expose the guts of his own profession. Breggin establishes that mental disorders cannot be authoritatively diagnosed by a chemical or biological test. Conclusive tests do not exist. And worse, in this undefined and arbitrary territory, the drugs that follow diagnoses are killers. For example, 300,000 cases of motor brain damage, as a result of the administration of major tranquilizers.

Under the Obama Plan, you can bet your bottom dollar that psychiatric care will eventually become mandatory. A patient suddenly diagnosed with clinical depression or bipolar disease will be told he must take the drugs—and suffer their adverse effects.

Science will take a back seat to a “share and care” collectivist philosophy, in which the so-called mental health of the individual is said to improve the group, the community, the nation. Under this cover, the attack on the individual personality will expand. Very young children will be given more and more debilitating and dangerous brain drugs.

These are no Luddite predictions. This is about hard fact, and those who shy away from the psychiatric literature and its fraudulent pretensions are whistling in the dark, pretending they are humanitarians of the first order.

Under the Obama Plan, it will be very convenient to declare new pandemics every few seasons, because these phony non-epidemics provide an opportunity to herd the sheep into clinics and remind them who is running the show. The United States will eventually become a Medical State, and lessons will have to be imparted on training wheels: go here, take this vaccine; go there, take that drug; the epidemic is endangering the herd, and you must help your brothers and sisters.

These are the figures on the last several “epidemics.” They are not yearly; they are totals, to date; global totals, except in the case of West Nile (US only):

SARS: 774 deaths.

WEST NILE: 1159 deaths.

BIRD FLU: 262 deaths.

SMALLPOX: (terrorist threat): 0 deaths.

SWINE FLU: 7909 deaths.

To give perspective, 250 thousand to 500 thousand people die of ordinary flu-like illness every year.

Yet this astounding death rate accrues no interest as an epidemic. It is only the “teaching (brainwashing) moments” of the phony epidemics that are promoted by health agencies (e.g., CDC and WHO) and their pharmaceutical allies, who rake in billions by manufacturing new vaccines.

Yes, under the Obama Plan, there will be more declared health emergencies, and they will serve to cement the citizen to his new role as eternal patient in the medical march along bleak streets of the future.

Can you perceive the loss of individual freedom implicit in this universal system of health control, and can you see how the present bill before Congress is the gateway?

[efoods]Do what you can to defeat the bill, and damn the torpedoes and syringes.

If you believe the US medical system is a beautiful thing in all its parts, and you want in, consider that other human beings don’t. You can have your wish, and you can help guarantee that your fellow citizens, who decline, can have theirs, too.

This country tends to run on slogans, and “healthcare for all” is the punch line being used to spread the word of a new era. But slogans don’t inform, they persuade. We’re at a moment when we need to see through the lie. The consequences are dire. The fake saints and prophets and their followers are preaching a message that contains a bomb.

Vast public ignorance about the US medical cartel and its true human effects is the delivery system for that bomb.

_________________________________

Sources and comments: I’m fully aware that people reading the facts in this essay will be shocked, and they will have doubts. Here are the sources for those facts. Things are not what they seem.

Barbara Starfield, “Is US health really the best in the world?” JAMA, July 26, 2000. Contains statistics on medically-caused deaths in the US.

On January 8, 2001, the LA Times ran a piece by Linda Marsa on the effects of medical drugs in the US. Predictably, the story sank like a stone. It provoked no Congressional hearings, no arrests.

The article described, in a few key paragraphs, a world of trouble. Adverse medical events. From med drugs.

“A 1998 University of Toronto study found that roughly 100,000 Americans die of adverse [medical-drug] reactions each year, and 2.1 million more are hospitalized.”

Marsa offered, in her Times article, a quote from an associate professor of medicine at Harvard, Dr. David Bates, an author of a 2000 study on drug effects. The study found that “18 percent of patients complained of drug-related complications…” Marsa wrote.

Here is the quote from Dr. Bates: “People often have [drug-caused] symptoms for months, but they’re either reluctant to let their doctor know or they weren’t sure if they just felt lousy…But these numbers translate to 36 million adverse drug events per year.”

Marsa dug out an explanation offered for this horrendous stat by the then-commissioner of the FDA, David Kessler.

Here’s Kessler’s quote from the Times article: “‘If an adverse event occurs in perhaps one in 5,000 or even one in 1,000 users, it could be missed in a clinical trial but pose a serious safety problem when released in the market,’ noted former FDA Commissioner David A Kessler in a 1993 JAMA article.”

Kessler was trying to explain (away) 100,000 deaths and 2.1 million hospitalizations and 36 million adverse reactions PER YEAR from FDA APPROVED DRUGS. He failed dismally. He seemed to be saying, “We can’t do any better.” If true, then Kessler and his colleagues should have abandoned the Agency and sought work elsewhere.

To add up the death totals from recent phony epidemics:

SARS—See WHO “Summary of probable SARS cases with onset of illness from 1 November 2002 to 31 July 2003” (based on data as of Dec.31, 2003).

BIRD FLU—See WHO “Confirmed Human Cases of Avian Influenza A (H5N1)” (24 September 2009)

WEST NILE—See CDC, West Nile Virus, Statistics, Surveillance, and Control. Years are reported separately, 1999-2009. I included only US cases because I couldn’t find a good source for global cases.

To confirm that every year, between 250,000 and 500,000 people die from ordinary flu, see WHO Fact Sheet No.211, Influenza (Seasonal).

Read Dr. Peter Breggin’s classic, Toxic Psychiatry, St. Martin’s Press, 1991. Follow Breggin’s argument, through several chapters, that labeled mental disorders are not based on factual biological evidence, and see p.89-91 for evidence that at least 300,000 people are suffering from brain damage (tardive dyskinesia) as a result of being administered major tranquilizers.

Under the centralized Obama Plan, control of the US medical system will fall into the hands of several powerful groups. The FDA, for decades a foe of alternative medicine, will increase its stranglehold on the nutritional-supplement market. Over time, it will enact tighter rules concerning what supplements may be sold to consumers and under what conditions. It will close down more alternative clinics. The Department of Health and Human Services will assume greater power over the states, and those states which now allow wide latitude to alternative health practitioners will be squeezed. The pharmaceutical industry, through its vast political connections, will accelerate its strategies to impoverish, bankrupt, and take over nutritional-supplement companies and gain control of that multi-billion-dollar market.

These trends will not necessarily be reflected in the laws governing the US medical-insurance plan, but those laws will create greater centralization, which translates into a pipeline of force for the major players.

Even a casual observer of the psychiatric landscape realizes that diagnoses of mental disorders are on the full upswing. The American Psychiatric Association, a wholly owned subsidiary of the pharmaceutical industry, will continue to exploit the mental-health market and enable the labeling of the majority of Americans with at least one mental disorder. That would be a target goal for Big Pharma. Again, this is not about credible science. It’s about business.

Founded in 1992, the National Center for Complementary and Alternative Medicine (NCCAM), a minor bureau of the National Institutes of Health (a federal agency), has managed to derail, stall, and divert the progress of real alternative medicine. It has forwarded no breakthroughs. It has bogged itself down in conferences, reports, and committee deliberations. It has fooled a number of so-called alternative-health advocates into believing that the federal government supports non-mainstream health strategies.

Imagine what will happen when healthcare in this country becomes centralized to a much greater degree under the Obama Plan. If this one tiny agency, NCCAM, can now befuddle the alternative field with a collection of inept and self-seeking bureaucrats, gargantuan power held at the top of the federal government will make that diversion look like a raindrop in a hurricane.

The modern medical system has always utilized PR to make its case to the public. Such efforts, under a federally run health system, will intensify by a factor of a hundred, a thousand. Its themes will run the gamut: toxic chemotherapy, radiation, and surgery for all cancers, even when the science confesses these treatments are useless and life-destroying; more vaccines for childhood illnesses, even though unvaccinated children experience these illnesses and emerge with natural immunity to them; unnecessary and damaging hysterectomies; frequent mammograms that lead to unneeded biopsies and mastectomies; “discoveries” about mental disorders that indicate the (false) need for debilitating drugs over the course of many years, for adults and children…

It’s important to realize that, at the heart of medical PR, success in applying dramatic treatments for emergency-crisis-trauma patients has been exploited, to make it seem that the same degree of success applies over the full range of medical intervention. Nothing could be further from the truth.

The history of the decline of infectious disease is a history of improved sanitation, an alleviation of overcrowding, the rise of the middle class, and above all, the betterment of nutrition. This decline in disease occurred before the introduction of antibiotics and widespread vaccination. Under massively centralized medical care, in an environment where chemically saturated agri-business grows our food in depleted topsoil, there is a greater and greater need for nutritional supplements. But this vital avenue will be narrowed and blocked in the ways I have indicated above.

In my 20 years as a medical reporter, I’ve documented instances in which germs were used as cover stories to explain away illness actually caused by horrendous environmental conditions. This inhuman operation is easy to understand once you realize that some of the leading pharmaceutical firms (which make billions by drugging germs) are also chemical companies (which sell enormous amounts of toxic pesticides) and are also genetic-engineering companies (which develop food seeds that yield crops with lower nutritional values, crops that demand more toxic pesticides to survive, crops whose adverse health effects remain untested).

Under a national medical plan, these companies would be able to assert even more power than they do now. The ease with which environmentally/chemically caused illness could be explained away “as a virus” would be child’s play, because the same people would hold the medical and chemical strings.

Last but not least, medical-research fraud continues unabated, an out-of-control rampant crime. Occasional confessions published in medical journals do not stop the fraud, whose major source is illegitimate pharmaceutical influence. Under a centralized government-run medical monolith, these offenses will become harder to spot and correct, and easier to portray as real science.

See, for example, “20 Percent Of Cancer Studies Report Conflict of Interest,” ScienceDaily (May 13, 2009): “Nearly one-third of cancer research published in high-impact journals disclosed a conflict of interest, according to a new study from researchers at the University of Michigan Comprehensive Cancer Center. The most frequent type of conflict was [pharmaceutical] industry funding of the study, which was seen in 17 percent of papers. Twelve percent of papers had a study author who was an industry employee. Randomized trials with reported conflicts of interest were more likely to have positive findings…”

Also, from the Boston Globe (Boston.com), “Flaws are found in validating medical studies; many see need to overhaul standards for peer review” (August 15, 2005):

“…after a study that sent reverberations through the medical profession by finding that almost one-third of top research articles have been either contradicted or seriously questioned, some specialists are calling for radical changes in the system…almost one-third of the top papers that appeared in top journals over a 13-year period from 1990 to 2003, had been either contradicted or found to have potentially exaggerated results. All the articles had [prior to publication] undergone vigorous peer review, leading to questions about whether problems should have been caught by reviewers…”


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