War on Health: Profits Before Patient Safety

Keep in mind, according to CDC statistics, no one has died from the use of food or dietary supplements, yet now, thanks to the FDA, you’ve got 3x as much regulation for food and dietary supplements as you have for pharmaceutical drugs, despite the fact that pharmaceutical drugs have proved to be one of the top killers of American citizens.

The relationship between physicians and the drug industry doesn’t begin once you have your MD or once you own your private practice; it begins the day you hit medical school. Big Pharma often give medical students gifts on their very first day. These gifts are always “Big Pharma” propaganda disguised as education, or something medical industry related that leaves the hard pressed medical student feeling like, at least someone cares, because we all know how tough medical school is.

But why is it so tough? Why are there intern boot camps?  Why must medical students and residents go through Why is "the private group that oversees physician training in the United States proposed rolling back rules so that young doctors just out of medical school can work shifts as long as 28 hours"? I mean, who wants an exhausted medical student/intern/resident practicing their craft on you when you are at your most vulnerable? Well one answer is that "medical school functions as a highly efficient system of inDOCtrination to ensure that physicians are less likely to question or confront the systems of power."

“Professors who have already been indoctrinated to think a particular way ensure discussions are kept "on topic," or within the traditional bounds of acceptable debate that do not challenge power. I personally have lost track of the number of times I have heard a professor say, "That is interesting, but it is just outside of the scope of the discussion we are trying to have." This is a highly efficient and subtle way of controlling thought.

It makes more sense when you consider modern medicine was founded by a robber barons and an oil tycoon in particular, John D. Rockefeller. The conspiracy to limit and eliminate competition from non-drug therapies began with the Abraham Flexner Rockefeller Report on Medical Education of 1910. Abraham Flexner was engaged by John D. Rockefeller to  “evaluate” the effectiveness of therapies taught in medical schools and other institutions of the healing arts. The Flexner report unequivocally recommended the closure of all the homeopathic and naturopathic medical schools, in other words, anyone or any institution who use natural medicines to heal.

Subsequently, federal alphabet agencies--FDA, CDC, etc.-- were created to enforce the allopathic model under the guise of "protecting" the American food and drug supply.   In actuality, these agencies serve the medical industrial complex, not American citizens as you will see in the following documentaries.  The reason is obvious: alternative, mostly inexpensive non-toxic therapies represent a potential loss of billions, if not trillions of dollars to allopathic (drug) medicine and drug companies, not to mention, there is nothing more threatening to elite power than a healthy, robust public.







Links:

Overdosed America: The Broken Promise of American Medicine by John Abramson, M.D.

AIDS, Opium, Diamonds, and Empire: The Deadly Virus of International Greed. by Nancy Turner Banks, M.D.

Treaties and International Agreements

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Mycoplasma, AIDS, Degenerative Diseases: What You Don't Know Can Kill You.

John D. Rockefeller  Sr.'s merger with pharmaceutical and chemical giant, I.G. Farben (Auschwitz was a 100% subsidiary of IG Farben) in 1928 "created the largest and most powerful cartel the world has ever known. Not only has that cartel survived through the years, it has grown and prospered. Today it plays a major role in both the science and politics of cancer therapy."

It's important to know Big Pharma's "crimes against humanity" history, because that history fostered the chemical-based drug treatment basis for our "orthodox" healthcare system today. The industry claims that their aim is finding medical truth, and that may be true; nevertheless, publicizing that truth, once found, if that truth entails inexpensive solutions or remedies, will not happen for obvious reasons. There is nothing Big Pharma likes more than chronic illness, for which they can produce chronic palliative costly treatments that make the patient chronically dependent on them.

Which brings me to the seldom, if ever, publicized human pathogen: mycoplasmas. They are the smallest free-living bacteria that can assume multiple shapes including round, pear shaped and even filamentous forms because they lack a cell wall. This makes it possible for them to pass through  filters used to remove bacteria; and hide inside the cell from our immune system, as well as from common antibiotics, all the while interfering with the cell machinery. Because mycoplasmas have lost most of their genetic material; a strict dependence on the host for nutrients and refuge determines its ability to survive and grow.

Mycoplasma is the co-factor that alters the human immune system and opens the door for the autoimmune degenerative diseases such as AIDS, malignant transformation, chromosomal aberrations, Chronic Fatigue Syndrome, Gulf War Syndrome (military vaccine), Amyotrophic lateral sclerosis (ALS), often referred to as Lou Gehrig\'s Disease (every single patient shows mycoplasmal infection), Alzheimer’s, Crohns Disease, Parkinson’s, Huntington’s, Lupus, Lyme disease, Fibromyalgia, Rheumatoid Arthritis, Multiple Sclerosis, Type One Diabetes, Autistic Spectrum Disorder, and cancer.  Yet, these pathogenic organisms show up in vaccines.

“Because certain species of the mycoplasma have an absolute growth requirement for the up-take of pre-formed sterols, including cholesterol they can cause the ‘spontaneous degeneration’ of the cells that they invade. If they do not cause sufficient damage to kill the cell, they at least compromise its capacity to defend itself from other disease agents, such as those which present as Kaposi’s sarcoma, pneumoniae carinii pneumonia, lymphadenopathy, and so on.” Donald W. Scott and William L.C. Scott,

“From its inception, the biowarfare program was characterized by continuing in-depth review and participation by the most eminent scientists, medical consultants, industrial experts and government officials, and it was classified Top Secret. The US Public Health Service also closely followed the progress of biological warfare research and development from the very start of the program, and the Centers for Disease Control (CDC) and the National Institutes of Health (NIH) in the United States were working with the military in weaponising these diseases. These are diseases that have existed for thousands of years, but they have been weaponized—which means they’ve been made more contagious and more effective. And they are spreading.” Donald W. Scott

Currently, Dr. Alan Cantwell is one of the most well-known popular proponents of the link between cancer and bacteria. He has written numerous articles and books on the subject after he isolated and reported cell wall deficient bacteria in breast cancer, Kaposi’s sarcoma and Hodgkin’s disease. He states,

”If a disease like cancer is indeed caused by microscopic bacteria, it would indicate physicians have been unable to see what was quite plain for some nineteenth and twentieth century scientists to observe using simple light microscopy."

Eventually, constantly under intense criticism, Cantwell was ostracized by many in the medical profession.

Females are four times more likely to be infected with Mycoplasmas than males. The same ratio of males to females applies to Rheumatoid Arthritis, Fibromyalgia, Chronic Fatigue and other related auto-immune disorders. Men, pound for pound, have 25% more blood; hence, hemoglobin - the protein molecule in red blood cells that carries oxygen from the lungs to the body's tissues - than females.

AIDS and Mycoplasma: The Crime Beyond Belief

Donald W. Scott, editor of The Journal of Degenerative Diseases (pictured above) and co-founder of the Common Cause Medical Research Foundation, reveals the true and hidden story of weaponized mycoplasma and the protracted creation of AIDS by governments and private corporations. part 1 of a series drawn from the 90 min. talk given at the 9th annual conference, Sudbury, Ontario (Aug 29-31, 2008).  JODD (Journal of Degenerative Disease); Box 133 Station B; Sudbury Ontario; Canada P3E4N5  $25/year





Links:

Fluid Mosaic Model Membrane

The Linking Pathogen in Neurosystemic Diseases

Mycoplasmas Stealth Pathogens

Campaign for Truth in Medicine

Mycoplasma Protocol

Institute for Molecular Medicine

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Prescription Drugs Kill More than Cocaine and Heroin Combined!

A recent study out of Brandeis University reveals that prescription drugs kill more people than most of the street drugs combined.  Meanwhile, our government--such as people like Dick Durbin and Dick Blumenthal-- are trying to ban vitamins and supplements under the guise of safety when they haven't killed anyone.

For instance,  banning vitamin B6, which is "naturally present in a variety of foods, and that is necessary for proper nerve function, protein synthesis, regulating blood sugar, and producing antibodies and hemoglobin.  But, while many people get their B6 through supplements, the U.S. Food and Drug Administration is looking to make things a lot more difficult—by slowly taking all forms of B6 supplements off the market so Big Pharma can make millions off of prescriptions instead.

According to the Alliance for Natural Health (ANH), the FDA has already begun their crusade. They removed Pyridoxamine (a natural form of B6) supplements from the market at the request of BioStratum, a pharmaceutical company.

Why? Because BioStratum thinks it might be nice to use Pyrdoxamine in a prescription drug. They haven’t developed the drug, we don’t know what it is, and who knows when it will come to fruition, but the FDA honored a request from the big corporation to protect the company’s interest. Now, the FDA is poised to pull another B6 product: P5P. You see, the human body must convert B6 to P5P to make it usable within the body. Fortunately, some supplement companies have created P5P and it is currently available as a natural supplement. But, another pharmaceutical giant has petitioned the FDA to “protect its interests."

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Watch How the FDA Suppresses a Cure For Cancer.

The following documentary is a MUST-SEE for everyone! I have yet to see anything so fully documented that exposes the extraordinary measures that the FDA will resort to in order to ensure that cancer remains the killer that it is, and  that Chemotherapy remains the torture-chamberous non-curing treatment that it is. Not to mention, this film, in addition to detailing the FDA's 14 year campaign to remove Dr. Stanislaus Burzynski, who found a cure for cancer, from society, also reveals the battle Dr. Burzynski had with the National Cancer Institute, who is just as bad.

"Our bodies contain two categories of genes that allow cancer to flourish: oncogenes, and tumor suppressor genes. When someone has cancer, they have a higher level of oncogenes switched on, with a higher level tumor suppressor genes switched off.

The goal is to tell the body to both switch back on the tumor suppressor genes, and turn off as many oncogenes as possible."

It comes to no surprise to most of us that the median annual American pharmaceutical company profits triples the median annual profits of all of the Fortune 500 companies. But, how does Big Pharma maintain these astounding profits? Well, through its gatekeeper: the FDA, and the National Cancer Institute.

"Big Phama" didn't manifest overnight. It was an ongoing process that started in the 1970s and 1980s.  At the time,  profitability of the pharmaceutical industry was two times greater than the median of all industries in the Fortune 500. In the 1990s, when the Prescription Drug User Fee Act (PDUFA)- which authorizes drug companies to pay "user-fees" to the FDA for each brand-name drug considered for approval, greatly speeding up the approval process - kicked in, the drug industry's profitability grew to almost four times greater than the median for all industries in the Fortune 500.

After the PDUFA was enacted, the part of the FDA that reviews new drugs received more than half its money from user fees and it grew by leaps and bounds.  Meanwhile, the part of the FDA that monitors safety, ensures manufacturing standards, and checks ads for accuracy deteriorated. Not only that, the approval process for brand-name drugs shortened to 3 months, from its previous 21 months. Yet, here it is 2011, and Antineoplaston Therapy has been waiting approval since 1977.

On June 21, 1977, Dr. Burzynski's attorney's investigated both state and federal law to find out if it was legal for him to start his own biomedical research company to make the Antineoplastons (non toxic cancer treatment) and administer them to patients within his private practice.  He found out it was legal as long as he avoided interstate commerce.

However, it was not soon after that Burzynski's patients found themselves harassed by the Texas State Board of Medical Examiners(TMB) to file charges against their doctor, and the FDA started its witch hunt.

In 1983, the FDA obtained an injunction from a federal district court prohibiting Dr. Burzynski and the Burzynski Research Institute from shipping antineoplastons in interstate commerce without first obtaining the approval of the FDA. The injunction, however, did not preclude intrastate distribution of the antineoplastons.

On July 28, 1986, the TMB began investigating Dr. Burzynski, even though no formal complaint had been filed, and on November 18, 1986, a notarized agreement between Burzynski and the TMB was created requiring the doctor resent a list of 40 successful cases.  He submitted double that number. He never heard back.

On September 6, 1988, the TMB convened a hearing to decide whether or not to revoke Burzynski's medical license. Texas State Board of Medical Examiners vs. S. Burzynski

Dr. Burzynski faced numerous battles with the federal government over the years. Between 1986 and 1994, he was subjected to three federal grand jury investigations. No indictments were ever handed down. However, during that time federal officials raided his research clinic and confiscated his patients' medical records.

Then in March 1995, Dr. Burzynski appeared on the CBS TV show "This Morning," accompanied by three of his patients. That very afternoon, the FDA raided his clinic again. A fourth federal grand jury investigation got underway, and by November 1995, charged Dr. Burzynski with 40 counts of distributing a non-FDA approved drug in interstate commerce, 34 counts of mail fraud, and one count of contempt of court for violating the order against interstate delivery of Antineoplastons. Rep. Joe Barton (R-TX) noted that a grand jury's failure to indict someone after three attempts is "virtually unprecedented."

On February 9, 1996, US District Court Judge Sim Lake ruled that Dr. Burzynski cannot treat patients outside of clinical trials. In other words, he issued a death sentence for hundreds of Dr. Burzynski's patients.

This prosecution marked the first time the FDA had tried to jail a scientist for using a drug on which he was conducting FDA authorized clinical trials. This trial alone, which was not even based on whether or not antineoplastons work or not cost the American taxpayer $60 million, while costing Dr. Burzynski over $2.2 million!

On March 4, 1997, due to a dead-locked jury, a mistrial was declared.

The FDA still did not back down. A second federal trial got underway May 19, 1997 to try Dr. Burzynski on the contempt of court charge. A federal jury acquitted Dr. Burzynski on May 27, 1997.

At the same time, Dr. Burzynski was fighting the Texas Medical Examiner's Board and the FDA, the National Cancer Institute, under Dr. Michael Friedman, tried to co-opt his discovery and render it ineffective.

A former employee of Dr. Burzynski, Dvorit Samid, betrayed him when she partnered with Elan Pharmaceutical through her employment with the National Cancer Institute and tried to hijack Burzynski's discovery. The problem was that she used only one component of the antineoplaston, phenylacetate, which when isolated, has very little clinical effect.

When that didn't work, the National Cancer Institute said they would accept Dr. Burzynski's antineoplastons; however, only if they could revise the protocol that Dr. Burzynski had perfected. Burzynski refused. The NIC threatened with patent infringement. Finally, they came to an agreement. Yet, within a very short time, in March 1995, the NIC tried to drastically alter Burzynski's protocol to make his treatment less effective!!

Four years after the NCI trials were closed and two years after Burzynski defeated the FDA, winning his freedom, the NCI, in February of 1999, decided to vindictively publish the scientifically invalid Antineoplaston trials in peer-reviewed medical literature. However, whoever published the invalid trials forgot to leave out the dosage, which in some patients was 2.7 times lower than the protocol demanded, and in other patients, 36 times lower, and, in even other patients, 170 times lower!

Li-Chuan Chen, PhD, who worked as a scientist for the National Cancer Institute from 1991-1997, said that when the NCI or assigned entities conducted trials on alternative cancer therapies they always altered the protocol and let it fail in order to discredit the therapy. He went on to say, "Scientists never look at it carefully, because as he says, Popeye is telling you something and you don't question him...under the capitalist sun, there is nothing sacred."

Here's the kicker. On October 21. 1991, the United States of America as represented by the Department of Health and Human Services, along with "Inventor": Dvorit Samid filed a patent for Antineoplastons. On October 12. 1993, the US and Dvorit Samid file for a second patent on Antineoplastons. And on March 7, 1994, the US and Dvorit Samid file its most comprehensive patent spanning 111 pages. Seven months later they file a fourth one. On 6/6/1995, the US files its 5th, 6th, 7th, and 8th extended patent. The next day, the US files its 9th, 10th, and 11th patent. A few months later, Dr. Michael Friedman leaves his position at the NCI and becomes Deputy Commissioner of Operations for the FDA, working directly under Dr. David Kessler.

In the three years (1997-2000) after Dr. Burzynski was indicted, all of the US patents for Antineoplastons were approved. However, one paragraph within these patents, in particular, is quite revealing:

Since 2009, the  only obstacle in the way of Antineoplasmons is the $300 million pricetag on the final phase of FDA clinical testing...and the FDA's requirement that children with inoperable brainstem glioma to also under go radiation treatment in these Phase 3 trials, claiming it would be unethical to do otherwise. 



Links:

Big Pharma Deals to Preserve High Drug Prices Skyrockedted in FYI 2010

The Truth About Drug Companies by Marcia Angell

Pay-For-Delay: How Drug Company Pay-Offs Cost Consumers Billions


Families USA

Bush Administration Back Pharmaceutical Industies Over the Needs of Millions of Senior Citizens

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If Technology is Advancing Exponentially, Why Does Oncology Remain in the Dark Ages?

Cancer's been around forever, it seems, yet very little progress has occured in its treatement. In fact, more people than ever are getting cancer, and, very often, the prescribed treatment: chemotherapy, is more lethal than the disease. Not to mention, the mental anguish, physical suffering, and poor quality of life cancer patients are encouraged to endure by almost every doctor who talk or scare them into undergoing chemotherapy.

So, if technology is advancing exponentially, why does oncology remain in the "dark ages"? Could it be the economics behind chemotherapy? In other words, cancer is big business, and healthy individuals interfere with the profit mechanism that depends on the proliferation of cancer patients. Something as simple and cheap as baking soda and sunshine is a complete anathema to the cancer industry. Promoting baking soda as an alternative treatment for cancer plunders the profits of the parasitic industries who sell themselves as our friends.

On the other hand, what do you have to lose from considering alternatives to this extraordinary costly, and barbaric form of cancer treatment that oncologists push today? Nothing, especially if you consider it before the "industry" gets a chance to wrap its parasitic tentacles around you.

When in doubt, ask yourself, cui bono ("To whose benefit?"). The answer is simple. The unscrupulous powers that work to maintain the status quo of the medical and pharmaceutical industry at any cost, including the lives of millions of people.

Dr. Tullio Simoncini scrapped the current cancer paradigm and started from scratch. His findings show cancer is caused by the progression of a fungus called Candida Albicans. Based on this hypothesis, Dr. Simoncini treats cancer with sodium bicarbonate, the most potent enemy of fungi, and his rate of success is encouraging.







And finally, a man named Vito Johnston, who claimed to have cured stage 4 prostate cancer with Baking Soda Molasses Cancer Protocol Solutions.

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Brain Eating Vaccine?

A chemically lobotomized, subservient public?

Some would say this has already occurred. However, up to this point, chemicals have not been necessary. We, the plugged-in masses, have succumbed to the brainwashing and propaganda channeled through the mainstream media, in an all out effort to distract us from the truth and ensure we remain ignorant, passive, insatiable consumers of everything, rather than interfering engaged, proactive citizens.  So far, chemical-free, systematic manipulation has worked wonders.

Then, the Internet came along. All of a sudden we, the people have a platform to fight the mainstream denial of real news and information, making it harder for the corporate media to whitewash reality with trivial nonsense like celebrity drama, reality TV and all of the other manufactured mind-numbing distractions. This new threat (Internet) to the power elite's over 30-year old "class piracy" assault on the well-being of average Americans may set  "Big Nurse" and her lobotomizing pharmaceuticals in motion.

“There will be, in the next generation or so, a pharmacological method of making people love their servitude, and producing dictatorship without tears, so to speak, producing a kind of painless concentration camp for entire societies, so that people will in fact have their liberties taken away from them, but will rather enjoy it, because they will be distracted from any desire to rebel by propaganda or brainwashing, or brainwashing enhanced by pharmacological methods. And this seems to be the final revolution.” - Aldous Huxley

So, brain-eating vaccines? Or inoculation for chronic stress?

Well, considering President Obama's science czar, John Holdren, co-authored a 1977 book that called for “planetary regime” to enforce totalitarian population control measures, the first option to seems the safest.

After 30 years of research into cures for stress, Dr Robert Sapolsky, professor of neuroscience at Stanford University in California, believes it is possible to alter brain chemistry to create a state of 'focused calm'.
...
In humans this engineered virus would short-circuit the neural feedback caused by stress, that lingering feeling of tension after a crisis has passed.
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'This could change society. It would leave you fresher and ready to deal with another threat, so you can maintain your drive, but with more focused calm rather than bad temper and digestion."
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After early setbacks, the Stanford team has adapted a herpes virus to carry engineered 'neuroprotective' genes deep into the brain to neutralise the rogue hormones before they can cause damage. The virus is now shown to work on rats.

Links:

Flouride and the Future: Population Level Cognitive Enhancement

The Corrupt World of Global Vaccine Politics

Repressed 60 Minutes episode on CDC/FDA/ADA Mercury Coverup

RFK, Jr on the vaccine autism cover-up.

Secret CDC Study/Report On Thimerosal

Thimerosal in Childhood Vaccines, Neurodevelopment Disorders, and Heart Disease in the United States

Toxic effects of mercury to excerabation of the medical condition classified as Alzeimer's Disease

Synergistic toxicity

Protocol for Mercury/Silver Filling Removal

Mercury in Medicine – Taking Unnecessary Risks

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