Following the Moves and Counter-Moves On the GeoStrategic Chess Board

Mass Killing of the Bradstreet Medical Research Team To Block New Cures For Cancer, Autism, and other Diseases

Preface:

The crimes against humanity of the concealed clique of foreign banking families in the City of London has reached a new high with its orchestrated elimination of the medical research team headed by Dr. James Bradstreet and the clique’s effort to hold back and block medical advances to benefit our species.

When the clique’s major profit centers are threatened, their playbook calls for a gradation of measures beginning with massive bribery, then blackmail, and then, if necessary, deadly violence.  In this case, the threat was to the clique’s golden goose, its burgeoning cancer treatment industry, including, of course, its monopoly control of the pharmaceutical industry.   Cancer is the number two cause of death in America and is projected to increase 75% by 2030, just 15 years away.

(http://health.usnews.com/health-news/news/articles/2012/06/01/worldwide-cancer-incidence-predicted-to-rise-75-by-2030). 

This incredible and intolerable situation is a broad clue that the clique’s concealed depopulation schemes are in full operation and dots immediately start to connect: the surge in cancer disease is being propelled by a clique scheme, already underway to push glyphosate levels up, as described by the article enclosed below: 

The EPA is set to raise “safe” glyphosate contamination levels. Notwithstanding several documented reports of the current dangers of glyphosate exposure, including one from international plant pathologist, Dr. Don Huber, the EPA sets out to dupe the public once again and declare that the current set levels for “safe” consumption of glyphosate should be raised. Expect this figure to rise periodically as levels of  contamination rise in proportion to the expansion of genetically engineered crops and their herbicide-resistant counterparts around the world.

Below is the video with Dr. Don Huber describing the machinations underway that are, in all likelihood, a key part of the clique’s effort to protect its medical treatment/pharma profit center and to carry on its scheme to reduce the world’s population by approximately 90%.  Pull up:  http://farmwars.info/?p=10945  and scroll down to the video.

The following material seeks to accomplish three purposes: 

(i) To lay out the deadly battle going on between independent medical researchers vs. the established medical/pharma cabal over the criminal supression of  breakthroughs in medical science and particularly gaining control over the eradication of cancer, the second largest cause of death in the U.S.;

(ii) To bring home the grim reality that the concealed clique exists, and a major part of its agenda, beyond forcing a one-world government on us, is its criminal psychopathic efforts, which are well underway, to exterminate 90% of the world’s population; and

(iii)  To kick the American and global public in their behinds until they wise up to the fact that the concealed clique EXISTS and is UNSTOPPABLE unless we immediately DEMOLISH their well-coordinated psychological warfare/propaganda apparatus that surrounds us with constant lies, deceptions, distractions, and disinformation. 

In other words, the concealed clique has A SECRET WEAPON that most of us don’t recognize.  We’ll call it a  PROPAGANDA/PSYOPS CANNON and in our imagination, let’s say that it looks like the image below.

____________________________________________________

This essential parts of this imaginary cannon are:

(i) the established, clique-owned media (newspapers and TV news);

(ii) the established, clique-owned entertainment industry;

(iii) the established, clique-owned system of “American Education;”

These three sources control nearly all of the information we receive and these three sources all follow the clique agenda exactly because they are all staffed with clique minions.  Accordingly, to get our American free press back in action, we have to demolish this cannon and send those who operated it to trial and life incarceration.

If we don’t, we won’t be able to find and maintain the truth about what is actually going on around us.

AND IF WE DON’T, THE CONCEALED CLIQUE WILL KEEP ALL OF US IN THE DARK UNTIL WE FINALLY FIND OURSELVES TRAPPED IN THEIR ONE-WORLD GOVERNMENT AS THEIR SERFS (or we will already have become a depopulation statistic).

Now, with that as a preface, you will understand why you will find some examples of the PROPAGANDA/PSYOPS CANNON firing away with constant lies, deceptions, distractions, and disinformation in the form of a number of Washington Post newspaper articles; the Washington Post being the most duplicitious, treasonous organization among its many established peers that make up what is called the mainstream media, which is currently an integral part of the clique’s global operation.

By 2014, the confidence level of the American public fell to 22% for newspaper sources, and fell to 18% for television news, which indicates a perceived untrustworthiness of the mainstream media. 

And there is just one American institution that is considered more untrustworthy than the mainstream media (establishment newspapers and TV news) and that is the members of the U.S. Congress, which has a public confidence level of only 7%.

REVEALED: Cancer industry profits ‘locked in’ by nagalase molecule injected into humans via vaccines… spurs tumor growth… explains aggressive vaccine push.

July 27, 2015

by Julie Wilson, staff writer

(NaturalNews) One of the world’s most lucrative industries, spending on cancer drugs reached an all-time high last year, as it was valued at more than $100 billion. Spending on cancer drugs increased 6.5 percent annually over the past five years and is expected to continue growing at a rate of 8 percent each year through 2018, according to figures provided by the IMS Institute for Healthcare Informatics.

That spending is highly concentrated, as the US and five of Europe’s largest countries account for nearly two-thirds of the entire market.

This means that billions and billions of dollars are secured by Americans being diagnosed with cancer.

That’s one profitable industry; however, it could all be completely dismantled by one thing: a cure.

As Mike Adams recently reported, “A universal cancer cure would destroy the profitability of the highly lucrative cancer industry and collapse the American Cancer Society, hospitals, oncology clinics and pharmaceutical companies that depend on chemotherapy revenues to stay profitable.”

This means that anyone moving closer to developing a cure for cancer would be considered an extreme threat to the medical establishment and likely stopped at any cost.

With that in mind, the mysterious deaths and disappearances of several natural health doctors throughout Florida is as suspicious as it is concerning.

If anyone was close to finding a universal cure for cancer and would ensure the public had access to it, it would likely be natural health doctors, or naturopaths, as they’re less likely to prescribe drugs and more likely to try and heal the body naturally using holistic medicine and nontoxic approaches.

Breakthroughs using this type of medicine are extremely “controversial,” as they threaten everything that the medical-industrial complex stands for, i.e. costly chemotherapy treatments and cancer drugs.

Doctors leading this type of research are routinely raided and shut down by the U.S. Food and Drug Administration (FDA), after which they’re treated like criminals and their reputations smeared.

This is typically orchestrated against doctors who are considered a threat by the medical establishment.

Renown holistic doctor found dead one week after FDA raids clinic

This seems to be the case with Dr. James Jeffrey Bradstreet, who was recently found dead after his body was discovered floating in a North Carolina river with a single gunshot wound to the chest. Bradstreet, a renowned physician known for his skepticism of immunizations (particularly the MMR vaccine), and his progressive autism research, was raided by the FDA one week before his mysterious death. The details of the raid remain largely unknown.

Personally affected by autism, as both his son and stepson were diagnosed with the condition, a significant portion of Dr. Bradstreet’s work was dedicated to this cause. He even testified twice before the U.S House of Representatives about the link between vaccines and autism.

As Natural News reported, leading up to his death, Dr. Bradstreet was working with a little-known molecule that occurs naturally in the human body. GcMAF (Globulin component Macrophage Activating Factor), which is the GC protein after it combines with vitamin D in the body, has the potential to be a universal cure for cancer.

It’s also believed to be capable of treating and reversing autism, HIV, liver/kidney disease and diabetes.

Dr. Bradstreet was working with a naturally occurring compound that may be the single most effective thing in the immune system for killing cancer cells

In an interview on the Hagmann and Hagmann Report, Dr. Ted Broer, an internationally recognized health and nutrition expert also based in Florida, describes how cutting edge Dr. Bradstreet’s work was, as well as a discovery he made that very well may have placed him in great danger and could have been the motive for his suspected murder.

The alternative doctors who went missing and/or were killed, were reportedly “interlocked” through Dr. Bradstreet and Dr. Gonzalez’s extensive research on autism, and what’s causing autism, according to Dr. Broer.

Dr. Gonzalez, a renown holistic cancer treatment pioneer who helped thousands overcome the disease through alternative medicine, died of an apparent heart attack just one month after Dr. Bradstreet’s body was discovered floating in a river.

Internationally recognized health and nutrition doctor reveals possible motive for Bradstreet’s death.

Dr. Broer stated in the interview:

This information I’m about to give you right now is extremely controversial and a bunch of people have exited the planet who were working with it.

This information has been around for awhile. They knew the information they were working with and they were basically being very, very careful, supposedly. And some of them were being accused of using GcMAF, and the FDA apparently raided several of their offices several weeks before they committed suicide or suddenly died.

It’s going to sound complicated, but I’m going to break this down for everybody super, super easy tonight. When you first hear these terms they’re going to sound weird to you.

GC protein is a protein in the body that’s used by macrophages in the body. What it does is, macrophages in the body are the ones that kill cancer cells, they stop cytokines storms and can be involved in cytokines storms, we’ll explain all these terms in a few minutes.

After defining GcMAF and how it’s formulated, Dr. Broer reiterates that it’s “probably the single most effective thing in the immune system to kill cancer cells.”

However, what Dr. Bradstreet and his colleagues discovered is that the immune system is being compromised by a compound called “nagalase.”

Nagalase is an enzyme/protein that’s made by cancer cells and viruses causing immunodeficiency syndromes and has also been linked to autism as well as a “host of other problems,” Dr. Broer explains.

Doctors found dead and/or went missing felt that nagalase was being introduced to the body through vaccines.

“What ends up happening is when the GC protein cannot be converted to McGAF, the entire immune system is compromised.”

Some of the doctors who wound up dead or missing believed that the nagalase protein/enzyme was being introduced intentionally into the body either virally or directly through vaccines.

“This is such incredibly damning information to the entire medical profession and the immunological profession and those folks that [sic] are producing immunizations, that apparently they didn’t want these guys around,” Dr. Broer said.

“I’m not saying what happened to these guys, I’m just saying they’re not on this planet anymore.”

Doctor compares cancer-causing nagalase to stealth bomber.

Nagalese blocks the GC protein from attaching itself to vitamin D, thus preventing the immune system from doing its job and therefore causing cancer and other serious diseases. Without an active immune system, cancer and viral infections can spread rapidly.

Remarkably, there’s a significant amount of research available on nagalase and the GcMAF protein. Citing a chapter from The GcMAF Book by Dr. Tim Smith, MD, Dr. Broer said:

Nagalase is like a stealth bomber, the nagalase enzyme synthesized in or released from cancer cells or a virus particle pinpoints the GcMAF protein facilities on the surface of your T and B lymphocytes and simply wipes them out with an incredibly precise bomb.

How precise? Nagalase locates and attacks one specific two-electron bond located only at the 420th amino acid position on a huge protein molecule, one of tens of thousands of proteins, each containing millions of electrons.

This is like selectively taking out a park bench in a major city from 6,000 miles away. More astonishingly, if that is possible, nagalase never misses its target, so there is no collateral damage.

Nagalase is being found in super high concentrations in autistic children.

Dr. Bradstreet and his colleagues also learned that the nagalase protein was not present in children at birth but was somehow introduced into autistic children, they felt, during the immunization process.

Before his death, Dr. Bradstreet treated 1,100 patients with GcMAF with an 85 percent response rate – something that was deemed impossible by the medical community.

After reintroducing GcMAF (which had been blocked by nagalase), 15 percent of Bradstreet’s autistic patients were no longer autistic, as all of their symptoms were completely eradicated.

Since 1990, 59 research papers have been published on the healing effects of GcMAF, 20 of which pertain to the treatment of cancer. Research suggests that GcMAF can also cure or effectively treat Parkinson’s and Alzheimer’s disease and rheumatoid arthritis, as well as reduce cancerous breast, prostrate and kidney tumors.

Commentary:  The clique has control of most of the sources of information available to the American and global public, which it uses to maintain a high wall of false reality that consists of lies, distortion, fabrication, disinformation, and psychological warfare directed at the public all for the purpose of creating an atmosphere of fear, uncertainty, doubt and mental disorientation.  To try to display this phenomenon, we will include the coverage of some if these incidents by The Washington Post, showing the two key sources of the articles, the executive editor and the reporter of the newspaper.

These three videos connects the dots between Dr. Bradstreet, GcMAF, cancer cures and the suppression of medical science by the U.S. government:

INVESTIGATION: Three days before Dr. Bradstreet was found dead in a river, U.S. govt. agents raided his research facility to seize a breakthrough cancer treatment called GcMAF

Monday, July 27, 2015

by Mike Adams

(NaturalNews) The history of the suppression of medical science in America is a long one, filled with true accounts of pioneering doctors and clinicians being threatened, intimidated and even assassinated in order to bury emerging cures and keep the “sick care” industry in control. (The American Medical Association, for example, has been found guilty by the U.S. federal courts of a conspiracy to destroy the chiropractic industry, by the way.)

Over the last few days, we’ve learned that before being found shot in the chest and floating in the river, pioneering medical researcher Dr. Bradstreet was working with a little-known molecule that occurs naturally in the human body. Called, “GcMAF”, this molecule has the potential to be a universal cancer cure for many people. It has also been shown to reverse signs of autism in the vast majority of patients receiving the treatment.

While GcMAF is perfectly legal as a treatment in dozens of advanced nations around the world, the U.S. Food and Drug Administration has outlawed it, calling it an “unapproved drug.” It is with this designation — an effort to suppress the forward progress of medical science — that the U.S. government conducted a raid on Dr. Bradstreet’s clinic, specifically seeking to confiscate GcMAF in order to shut down his research and halt his treatment of patients. Meanwhile, Big Pharma gets special permission to unleash untested, experimental drugs on the public as long as those drugs earn sufficient profits.

In this article, I summarize the videos, articles and documents covering GcMAF and the mysterious death of Dr. Bradstreet. An exhaustive investigation needs to be pursued on this matter, possibly involving private investigators. The timing and manner of Dr. Bradstreet’s death seems highly suspicious, especially in light of the many other holistic doctors who have recently been found dead under mysterious circumstances. (Dr. Nicholas Gonzalez died just days ago…)

Motive to murder medical researchers and suppress a promising cancer treatment breakthrough

Is there a motive for the murder of pioneering cancer researchers working on a possible universal cancer cure? Of course there is… it’s the most common motive in the world: MONEY.

A universal cancer cure would destroy the profitability of the highly lucrative cancer industry and collapse the American Cancer Society, hospitals, oncology clinics and pharmaceutical companies that depend on chemotherapy revenues to stay profitable. Key to their profitability is the inescapable fact that conventional cancer treatments simply don’t work most of the time, creating a reliable profit stream of repeat business from patients who are never cured (by design).

Would the cancer industry murder doctors to protect its profits? Of course it would. The industry kills patients as a routine part of its business operations! For example, an oncologist named Farid Fata was recently sentenced to 56 years in prison for falsely diagnosing patients with cancer so that he could sell them chemotherapy treatments they didn’t need. See the article Cancer doctors ‘fess up to making false diagnoses just to make more money.

Click here to search for “cancer false diagnosis” at GoodGopher.com, the search engine for truth seekers.

INVESTIGATION: Here’s what we know so far

Multiple hat tips to all the outstanding citizen journalists, video creators and bloggers who have created the items cited below:

U.S. govt. search warrant document served against Dr. Jeffrey Bradstreet to confiscate GcMAF from his research facility.

HealthNutNews story that covers the apparent series of murders of holistic doctors, many of whom are working on advanced treatment protocols that render high-profit sectors of conventional medicine OBSOLETE:

Yet another doctor was just found murdered inside his home here on the East Coast of Florida. This makes six doctors to be found dead in the last month just from this region of the country alone. Four out of the six were found dead here in Florida. We lost the holistic Dr. Teresa Sievers, MD, who was found murdered in her Florida home just weeks ago. We’ve also lost the alternative Dr. Jeff Bradstreet, MD, who was found in a river with a gunshot to his chest. He’d recently moved to Georgia from Florida. We’ve also lost the Osteopath. Dr. Riley, who was found in Georgia at her home; just a few hours from the Florida border. She was found with a gunshot wound to her head.

Now we’ve lost Dr. Schwartz MD, who was found murdered in his home, on Sunday, July 19th, 2015. This was four weeks to the day after the death of the first physician: (Dr. Bradstreet MD) who I broke the story on a month ago. His family is still seeking answers as to what happened to him and they’re some of the kindest people I know. The latest MD, Dr. Schwartz, in the picture above, lived just north of the fit, healthy, holistic Dr. Hedendal; who was the second doctor to be found dead this past Father’s Day, in Boca Raton. This was the same day that Dr. Holt died at the age of 33. Both were fathers; and again, both men died here in Florida on June 21st, 2015.

SCIENCE.NaturalNews.com entry describing the extraordinary benefits of GcMAF in a published study:

Stepwise incubation of purified Gc protein with immobilized beta-galactosidase and sialidase generated probably the most potent macrophage activating factor (termed GcMAF) ever discovered, which produces no adverse effect in humans…

After about 16-22 administrations (approximately 3.5-5 months) of GcMAF, these patients had insignificantly low serum enzyme levels equivalent to healthy control enzyme levels, ranging from 0.38 to 0.63 nmole/min/mg protein, indicating eradication of the tumors. This therapeutic procedure resulted in no recurrence for more than 4 years.

In other words, the administration of GcMAF eradicated tumors and left patients cancer-free for 4+ years with no additional treatment!

Both U.S. and UK governments desperately seizing all supply, shutting down clinics, even as millions die from cancer every decade…

UK govt. admission that GcMAF was on track to being commercialized as a pioneering cancer treatment, so they had to confiscate it!

GcMAF (Globulin component Macrophage Activating Factor), a blood product, claims to treat a range of conditions including cancer, HIV and autism…

More than 10,000 vials were seized at this site and production of this unlicensed medicine has now ceased. These products were sold through various European websites and UK patients may have bought it from one of these websites. We are working with colleagues in other countries to alert them to the potential risks. Our investigations are ongoing and we have received no reports to date of side effects caused by this product.

That same page lists some of the websites where GcMAF had been available for purchase:

http://www.GcMAF.eu
http://www.immunobiotech.eu
http://www.immunocentre.eu
http://www.petgcmaf.com
http://www.firstimmune.fr
http://www.firstimmune.de
http://www.firstimmune.it
http://www.gcmaf.gr
http://www.gcmaf.se
http://www.gcmaf.es
http://www.gcmaf.ru
http://www.gcmaf.pl

GcMAF is readily available as a medical treatment in Japan. This site explains:

GcMAF (Gc Protein derived Macrophage Activating Factor) – Gc MAF treatment is a highly effective macrophage activating therapy, used to stimulate the immune system and activate macrophages so that they can destroy cancer cells and other abnormal cells in the body.

From the FAQ page of the treatment clinic:

What exactly is Second Generation GcMAF?
High Dose Second Generation Gc-MAF is produced using our new Patent Pending process which was developed here in Japan by Saisei Mirai in collaboration with Dr Hitoshi Hori and Dr Yoshihiro Uto at the University of Tokushima who have been studying GcMAF for over 20 years. Studies on GcMAF began at the University of Tokushima in 1992, after they were introduced to Dr Nobuto Yamamoto’s work and a collaboration began…

Second Generation GcMAF is made using a new and improved 2nd generation method of Gc-MAF production which is 10-20 times more concentrated and is more active and stable than other GcMAF that is currently available. Importantly, this much higher concentration GcMAF has been clinically demonstrated to be largely free of any side effects in the great majority of patients and is much more stable because it is resistant to oxidation.

That same site describes Oral GcMAF as follows: “Oral GcMAF is a form of GcMAF produced from bovine colostrum by Saisei Mirai which was developed in collaboration with Tokushima University.”

It also lists the following health conditions as being treatable with GcMAF, potentially a “universal cancer cure” substance:

Gc-MAF and/or oral Colostrum MAF macrophage activation therapy is indicated in the treatment of any diseases where there is immune dysfunction or where the immune system is compromised, such as:

Cancer
Autoimmune diseases
Epstein-Barr Virus (EBV)
Hepatitis B virus (HBV)
Herpes Simplex virus (HSV)
Cystitis
Hepatitis C virus (HCV)
Multiple sclerosis (MS)
Urinary tract infection (UTI)
Autism Spectrum Disorders (ASD)
Rheumatoid arthritis (RA)
Endometriosis
Chronic Fatigue Syndrome (CFS)
Lyme disease (Lyme borreliosis)
IgA deficiency disorder
Myalgic Encephalomyelitis (ME)
Mycobacteria infections
Parkinson’s disease
Tuberculosis
Fibromyalgia
Human papillomavirus (HPV)
Lupus (Systemic lupus erythematosus, SLE)
HIV AIDS
Dengue fever
Pneumonia infection
Warts caused by viral infection
Norovirus
Malaria Influenza virus (flu)
Herpes simplex virus (HSV)
Q fever (Coxiella burnetii)
Polycystic ovary syndrome (PCOS)
Chicken pox (varicella zoster virus)
Psoriasis
Respiratory tract infections
Ulcerative colitis, Crohn’s disease
Type 1 diabetes (T1DM), insulin-dependent diabetes (IDDM)
Type 1.5 diabetes, Latent autoimmune diabetes of adults (LADA)

Do you see yet why the medical establishment must SUPPRESS GcMAF and destroy all knowledge of its clinical applications? This one substance holds the potential to render numerous vaccines and pharmaceuticals utterly obsolete.

GcMAF protein described at NaturalHealth365.com:

Researchers and practitioners have demonstrated that GcMAF can reverse diseases that attack the immune system such as: chronic inflammation, bacterial and viral infections, chronic herpes, chronic acne, Lyme disease, fibromyalgia osteoporosis, Hodgkin’s, Lupus, MS, Parkinson’s and remarkably – autism.

A clinical study out of Italy on 94 children with autism showed that 83 of them made considerable progress while on GcMAF. The most common reported improvements involve:

• Cognitive abilities including attention and focus, learning and understanding, receptiveness and awareness of the environment and both receptive and expressive language gains.

• Social Skills including willingness to interact and communicate with peers.

• Behavior including less hyperactivity, less stereotypical behaviors and improved cooperation and compliance.

In another study of 1500 children with autism, 85% had high levels of viruses and a compromised immune system. All 1500 received weekly GcMAF injections and 70% of the children responded to the treatment with reduced symptoms and another 15% made full recoveries. The other 15% did not respond.

It was stated that the reduction of autistic symptoms is permanent provided that GcMAF has been taken long enough for the body to produce its own GcMAF which typically takes 24 weeks.

The systematic suppression of medical science to protect the lucrative cancer treatment industry (chemotherapy, oncology, radiotherapy, etc.)

ANH-EUROPE.org covers the systematic suppression of advanced cancer treatments and cures:

Back in 1993, Nobuto Yamamoto, then working at Temple University School of Medicine in Philadelphia, PA, USA, first described a remarkable molecule. His paper reported the conversion of vitamin D3 binding protein (DBP, known in humans as Gc) into a potent macrophage-activating factor (MAF), known as Gc-MAF. Macrophages are a key part of the human immune system with two roles: to engulf and destroy pathogens and cellular debris, and to recruit other immune cells to respond to the pathogen.

Gc-MAF hasn’t had the benefit of a single patent owner – as a natural molecule, it cannot be patented without being modified – with the will and resources to push it under the noses of the public and health authorities. Dr Yamamoto has run small human trials in breast, prostate and colorectal cancers, with promising results.

David Noakes might just be the person to bring Gc-MAF into the mainstream. He’s the CEO of Immuno Biotech Ltd. and spokesperson for First Immune Gc-MAF, a project he describes as, “PhD and BSc biochemists and biomedical scientists… with external doctors, oncologists and scientists who kindly provide advice, committed to bringing some of the increasing number of published but relatively unused medical cures to as many people as we can.” At the moment, Noakes and his colleagues are supplying Gc-MAF to 30 countries where it is legal, via a network of “around 300” doctors. Their Gc-MAF is made to extremely high standards, and is being used in ongoing clinical research by Noakes’ collaborators and others. Their ultimate goal is to, “Build the case that GcMAF is effective for various illnesses, which will help to make it available to the public”.

GcMAF suppliers fighting for survival against a global medical monopoly that profits from disease

MUST-SEE website: http://gcmaf.se/

From the site:

The medical laws have been changed over the last 40 years so that all the brilliant breakthroughs in cancer are denied to the British public. Lord Maurice Saatchi had to watch his wife die, while his doctor told him the only thing he was allowed to prescribe her was chemotherapy, which would shorten her life. He hopes to bring the Medical Innovation Bill to Parliament, so instead of obeying a destructive government law, a doctor will be able to prescribe whatever treatment is best for the patient…

Bad law kills, and Britain has the worst medical laws in Europe. The 1939 Cancer Act makes it illegal to discuss the possibility cancer can be cured, which is partly why 160,000 people die unnecessarily of cancer in Britain every year. Science and treatments are decades ahead of where the medical industry is today. The MHRA’s job is to get life saving treatments like GcMAF out to people as quickly as possible. Instead they block them to protect billion dollar Big Pharma monopolies, who also fund the MHRA. Over a hundred thousand lives could be saved every year if the 1939 Cancer Act were repealed, and the MHRA were closed down.

There are 142 eminent scientists who have published GcMAF research papers on the US National Library of Medicine alone.

From the how GcMAF works page:

Your GcMAF empowers your body to cure itself. In a healthy person your own GcMAF has 11 actions discovered so far, including two on cells, three excellent effects on the brain, and 6 on cancer. Amongst these it acts as a “director” of your immune system. But viruses and malignant cells like cancer send out an enzyme called Nagalase that prevents production of your GcMAF: that stops its 11 beneficial effects, and neutralises your immune system. So diseases become chronic, and cancer cells grow unchecked.

Minutes after a receiving a dose, 10 of the body’s actions restart. In three weeks of two GcMAF 0.25ml doses a week, your immune system is rebuilt to above normal strength. You need two doses a week for typically 24 weeks for many diseases and early cancers, up to seven one ml doses a week and a year for stage 4 cancers. Your body then takes the disease down without side effects, and successfully in 80% of cases -depending upon how well you follow the protocol under “Treatment Protocol” on this website.

What is GcMAF?
It is a human protein. One week’s GcMAF looks like a small raindrop. If properly produced it is perfectly sterile, and a most ethical course for doctors.

GcMAF is therefore a replacement therapy for those who can’t make their own. Taking GcMAF replaces the missing part of the immune system, and also acts as the body’s own internal medicine.

GcMAF is extracted and isolated; its a 24 step process, and at the end it must have tests to prove its sterility and activity. (If it does not come with published tests, its probably not GcMAF.) One GcMAF has been tested in universities, laboratories and clinics, where, as a result of the testing, consistent activity and sterility have always been found, and been the subject of 40 scientific research papers.

What does GcMAF do?
The GcMAF Conference 2013 showed GcMAF is a far more powerful molecule than thought, both in terms of the science, and doctors’ results. In stage 4 cancer, some doctors who use the full protocol, listed on “Treatment Strategies,” are saving every patient (if they have not had chemotherapy.) Success can be achieved with all tumour cancers including breast, lung, prostate, pancreatic and melanoma.

GcMAF can eradicate chronic inflammation and viral infections. It is better than antibiotics in many areas, and 25% successful with Autism, 50% or more with Chronic Herpes, Chronic Acne, Chronic cirrhosis of the liver, Chronic kidney disease, Chronic depression, Colitis, Crohn’s, Fibromyalgia, Hepatitis, Herpes, LMBBS, ME/CFS, Osteoporosis, Periodontal disease, Psoriasis and various types of Immune dysfunction including allergies. Research shows GcMAF can halt deterioration in Parkinsons, multiple sclerosis (MS), dementia and ALS, and in its role of immune system regulator, can reverse diseases that attack the immune system like Lupus and Arthritis. And is effective with wound healing. Its successful with tumour cancers, and some others.

In addition to rebuilding a depressed immune system, GcMAF:
Inhibits angiogenesis – stops blood supply to tumours
Activates macrophages – phagocytosis and destruction of cancer cells
Apoptosis – suicide of cancer cells
Reverts the cancer cell phenotype to normal (Turns cancer cells into healthy cells)
Reduces the metastatic potential of human cancer cells in culture.
Increases energy production at the mitochondrial level – ME/CFS
Improves human neuronal metabolic activity through cAMP signaling – autism, ME/CFS, MS, ALS
Counters toxic effects including cadmium – ME/CFS

It abolishes neuropathic pain due to neuro-oxidative stress (stress due to the anti-cancer drug oxaliplatin) in the lab. (neurodegenerative diseases and autism that have oxidative stress as a pathogenetic mechanism)
It increases neuronal connectivity by promoting differentiation and the formation of dendrites and neuritis (autism and ME/CFS, where there is a lack of connectivity between neurons).

See the 31 research papers published, particularly Brescia, and the 60 published by others listed under “The science”.

80% of terminal stage four tumour cancers cases can be saved (40% if they’ve had chemo), but usually when they are closely monitored, which is why residential Treatment Centres are being run in Switzerland. If they have three months to live and have not had chemo, almost no one needs to be lost.

The 180 scientists who have published papers on trials of GcMAF selected those in the early stages of cancer and HIV, and reported nearly 100 percent success, with no recurrence after many years. They did not attempt trials on people with large tumours.

Our trials are quite different: many people are over 50, some over 80, with advanced or terminal cancers, with significant tumour mass. Most come to us when their doctors tell them they can do no more.

The life of GcMAF is only six days – you have to keep taking it until your disease has gone (ie your nagalase is under 0.65 nmol/min/mg) then a further 8 weeks, or the immune system gets shut down again.

How long should you take GcMAF for?
8 weeks for chronic herpes/acne, fibromyalgia, inflammation.
Allow 24 weeks plus of GcMAF for: Autism (85% improve, 25% eradication), CFS (70% eradication), HIV, Lyme (8% respond, most appear to have the VDR gene blocked and the viruses conceal themselves with biofilms) and stage 1 to 2 cancer, (80% respond).
Late stage cancer, if you follow “Treatment Protocol” again has 80% responders, but it takes a year to 18 months to become cancer free.
Cirrhosis of the liver: 16 months

Remember everyone responds differently. We can’t say how you will respond.

The more minor the disease, the easier it is for GcMAF to eradicate. GcMAF needs normal levels of vitamin D to function strongly (take 10,000iu a day). in low responders, larger doses are required.

We have probably proved GcMAF can work for people up to age 90, and can destroy large tumour mass. See “Participants experiences”.

If you have your blood taken for monocyte counts, relevant markers and vitamin D levels, and again for a nagalase test at the beginning, you should see on your next test after three weeks that your immune system is back to full strength, and after 8 weeks significantly falling nagalase will indicate the disease is losing its grip. Don’t stop the GcMAF until your nagalase gets below 0.65 nmol/min/mg, when it loses the ability to prevent your body producing your own GcMAF, and then you no longer need ours. Even better, get scans.

Autism children can improve at five weeks with substantial improvements at 8 weeks. See “Participants experiences.” But everyone is different.

The beauty of using your own immune system to attack disease or cancer is that it remembers how to defeat it for the rest of your life: it doesn’t come back. And unlike chemotherapy, the side effects are trivial.

The only way you can tell if GcMAF is genuine and active is to test with living cells in a laboratory. See “Quality and Tests of our GcMAF.” To recap:

We put live macrophages cells and MCF7 breast cancer cells together; nothing happens. Then we add GcMAF; in 72 hours the macrophages eat all the MCF7 cancer cells. We then put only GcMAF and MCF7 together, and the GcMAF turns the cancer cells back into healthy cells.

We have GcMAF available for preclinical trials. See “Buy GcMAF”.

You must read at least all of “Buy GcMAF” and “Treatment strategies” on the left if you want to take this further. And you must be prepared to give us feedback.

Patent document on GcMAF

See the Yamamoto patent involving GcMAF:

Cancerous cells and HIV-infected cells secrete -N-acetylgalactosaminidase into the blood stream, resulting in deglycosylation of serum Gc protein. This inactivates the MAF precursor activity of Gc protein, leading to immunosuppression… When peripheral blood monocytes/macrophages of 175 cancer patients bearing various types of cancer were treated in vitro with 100 pg GcMAF/ml, monocytes/macrophages (phagocytes) of all cancer patients were activated for phagocytic and superoxide generating capacity. This observation indicates that patient phagocytes are capable of being activated…

Also see BetterHealthGuy.com coverage on GcMAF:

first heard about GcMAF almost a year ago. At the same time, I had first learned about “nagalase”, a blood test that is used to in part determine whether or not one might be a candidate for GcMAF therapy. Nagalase is an enzyme that prevents Vitamin D receptors (VDR) from being activated on the surface of the macrophage. As a result, macrophages are not “activated” and our immune systems are not able to properly respond to invaders.

Here are some points that I have learned thus far on GcMAF:

– GcMAF has reportedly been tested more for safety, purity, etc. than other human blood products.
– Macrophages are cultured, destroyed, and the GcMAF receptors are purified.
– Treatment is via injection 1x/week for 8-20 weeks. Dose is titrated initially to avoid exacerbation or Herx responses as much as possible.
– A commonly used dose is .25ml once weekly (a 2.2 ml vial should last 8 injections).
– The primary test used in looking at whether or not GcMAF may be a reasonable intervention is nagalase.
– Nagalase inactivates macrophages.
– I personally would NEVER consider this option without having a baseline nagalase test. Normal is < 0.95. Mine was 2.9.

The practitioner I worked with suggested that 2.9 was in the range of someone with HIV or cancer in terms of the impact on the immune system. I’d like to hear from others in the Lyme community as you get test results as well to see if there is a pattern of elevated nagalase in those with Lyme disease. Whether or not Lyme itself has anything to do with nagalase elevation is something I have not been able to find anything on. We certainly all have underlying viral co-factors that are likely in play as well, but I suspect that Borrelia may also play a role in nagalase elevation.

– In healthy college students, a nagalase 0.4 is not uncommon (the lower the better).

– At 2.9, my practitioner was surprised that I did not have more cognitive deficits such as memory loss and other cognitive issues.

– It has been suggested that ongoing antimicrobial therapy without a working immune system is like leaving the house with the door wide open inviting burglars in. By using GcMAF to activate macrophages, nagalase drops, and one may regain a functional immune system. The door is then closed to further invaders and we may no longer serve as a microbe hotel.

– Maintenance therapy should not be needed once the immune system is once again properly functioning.

– Activated macrophages only remain active for 7 days so any negative responses are generally short-lived. That said, some people do have strong inflammatory responses that are not believed to be typical die-off reactions.

– It has been indicated that in some cases, other medications may be needed in order to manage the inflammatory response. This is another reason that one needs to be working closely with a knowledgeable practitioner before considering GcMAF in my opinion. In the CFS and GcMAF world, this more severe form of a die-off reaction is called IRIS.

– VDR genetics do not seem to play a role in predicting response as earlier thought according to one practitioner that I have spoken with. That said, Vitamin D levels do correlate with the positive response rate of GcMAF. Thus, Vitamin D supplementation may be required in order to optimize outcome.

– Other than die-off reactions or activation of symptoms (inflammation), no other side effects are generally expected.

– Nagalase should be monitored every 1-2 months while on treatment to determine the required duration of the therapy. Target nagalase after treatment would be 0.4 to 0.6.

– Elevated nagalase has a profound detrimental effect on the immune system. Elevated nagalase is often presumed to be related to microbes of viral origin or cancer. Viruses that are nagalase producers open the door to chronic infections.

– Hemagglutinin contains nagalase and is also found in flagella of some bacteria so it could also be the case that some bacteria may produce nagalase.

– Parents with ASD children also often have elevated nagalase.

– A practitioner I spoke with likened Lyme disease to a “peat moss fire” burning below the surface. Activating macrophages should help to deal with the fire.

– GcMAF should be helpful in dealing with other infections that are not of viral origin; for example, Borrelia, Bartonella, and other infections commonly associated with Tick-Borne Infections (TBIs). GcMAF is active against many cancers and many different kinds of microbes.

– Neopterin is another test that is sometimes used as an indicator of immune suppression. As macrophages become activated, neopterin may rise and later fall. If one is in the normal range for neopterin and has an immune-related illness, this could be an indication that the immune system is suppressed and not responding appropriately.

– People with autoimmune conditions can generally use GcMAF. However, GcMAF may be contraindicated in people with Multiple Sclerosis.

– Reduction in nagalase is generally seen early in the course of treatment; within the first 3-6 weeks. In some studies, nagalase dropped by over 50% in less than six weeks.

– Cancer patients may initially feel as bad on GcMAF as they do on chemotherapy, but often feel much better after the first month.

– Anti-inflammatories may limited the effect of GcMAF.

– Enzymes and biofilm-reducing supplements may have a negative impact on GcMAF therapy and may be best avoided. It is still too early to know what the impact may be, but one practitioner I spoke with feels that it is best to avoid these.

– One should not be on any immune-suppressing agents while on GcMAF as the immune system must be partially functional in order to respond appropriately to the treatment.

– A common pattern is to see elevated lymphocytes, high nagalase, and low NK cells. Once nagalase drops, it may be the case that NK cell function could be positively impacted. CD57 is a type of NK cell. It is too early to know if this proves to be true, but it is one of the things I’m quite interested in.

Watch this video presentation on GcMAF therapy to learn more.

Read about GcMAF from Alternative-Health-Group.org.

Read The GcMAF Book at this link.

Open the “Stop Fighting Cancer” PDF document and search it for “GcMAF” to read some intriguing passages:

Researchers testing GcMAF stated it, “works 100% of the time to eradicate cancer completely, and cancer does not recur even years later.” (This was stated based on the tested group of patients -nothing works 100% for everyone) The weekly injection GcMAF, a harmless glyco-protein activates the human immune system which then can kill the growing cancer. Studies among breast cancer and colon cancer patients produced complete remissions lasting 4 and 7 years respectively. This glyco-protein ‘cure’ is totally without side effect but currently goes unused and completely ignored by cancer doctors. Why? Maybe it is because there is little money to be made in selling it. For less than $2000USD a cancer patient can obtain an adequate amount of GcMAC.

See the National Library of Medicine page Immunotherapy for Prostate Cancer with Gc Protein-Derived Macrophage-Activating Factor, GcMAF:

When human macrophages were treated in vitro with 100 pg GcMAF/ml for 3 hours and a prostate cancer cell line LNCaP was added with an effector/target ratio of 1.5, approximately 51% and 82% of LNCaP cells were killed by 4 and 18 hours of incubation, respectively [14,15]. This in vitro tumoricidal capacity of macrophages activated by GcMAF led us to investigate the therapeutic efficacy of GcMAF for prostate cancer. GcMAF therapy as a single remedy modality can eradicate metastatic breast and colorectal cancers most effectively…

Click here to search for “GcMAF” on GoodGopher.com, the new search engine for truth seekers.

Heads-Up:  While there is a great deal of startling information to absorb, one early realization is the possibility that the cancer disease is a planned epidemic that is scheduled to increase in intensity.  Think about it:  Cancer is the second largest cause of death in America and it is projected to increase by 75% by 2030—-that is just 15 years from now.  That leads to the notion that cancer may, in fact, has been and may continue to be a central part of the clique’s depopulation master plan.  And with that level of importance to the clique, any cure to cancer must be immediately be erased along with the people who are involved.  In other words, the swift disposal/disappearance of Dr. Bradstreet’s medical group can be much better understood if we consider that the intentionally induced rise of cancer has been earmarked by the clique as a core weapon in their depopulation schemes and the clique has extraordinarily high profit expectations by holding the world medical system hostage to current and largely ineffective cancer therapies, consisting of pharmaceutical products, chemotherapy, and surgery. 

Improved living standards in countries with a lower HDI may lead to a decrease in some infection-related cancers, but these countries may see a sharp increase in the types of cancer currently seen in higher-development countries, the researchers pointed out in a journal news release.

Cancer incidence rates could increase by 93 percent in low HDI countries by 2030, and by 78 percent in medium HDI countries (such as South Africa, China and India) over the same period, according to study leader Dr. Freddie Bray, of IARC, and colleagues.

The investigators also found that rates of prostate cancer and female breast cancer appear to be rising in most countries with medium, high or very high levels of development, and that rates of stomach cancer and cervical cancer are generally decreasing in countries with medium, high or very high levels of HDI.

Lung cancer is currently not a leading type of cancer in low HDI countries, but that will change unless smoking is effectively controlled in these countries, the study authors noted in the news release.

The researchers also found that 40 percent of worldwide cancer cases in 2008 occurred in countries with very high HDI levels, even though they had just 15 percent of the global population.

We now move to how the concealed clique uses its psyops/propaganda weapon, i.e., its control of media, entertainment, and educational systems, to keep the public in the dark about any issue then clique wants to remain concealed.   You can now assess the journalistic standards of The Washington Post, a cornerstone of the establishment media, by studying the following two articles pertaining to Dr. Bradstreet’s work.

Anti-vaccine doctor behind ‘dangerous’ autism therapy found dead, Family cries foul.

June 29, 2015

____________________________________________

By Michael E. Miller    Martin Baron, Executive Editor

James Jeffrey Bradstreet’s life was full of controversy.  To thousands of supporters, he was a savior: a physician who claimed vaccines caused autism and promoted radical procedures to treat those afflicted, including his own son.

To many others, however, he was a crackpot: a man who, despite his medical license, ignored science and championed dangerous, discredited and occasionally deadly treatments.

It’s no surprise, therefore, that Bradstreet’s death is proving equally divisive.

On the afternoon of June 19, a fisherman spotted Bradstreet’s lifeless body lying in the Broad River in the tiny town of Chimney Rock, N.C. He had a gunshot wound to his chest, authorities said. A gun was found in the water nearby.

That’s about all that everyone can agree on.

Like his research, Bradstreet’s death has become a Rorschach test in which his supporters see a conspiracy, while most everyone else — including law enforcement — sees a slow downward slide towards suicide.

The Rutherford County Sheriff’s Office said it is investigating Bradstreet’s death, but that the wound appears to have been self-inflicted.

Bradstreet’s family, however, has set up an online account to raise funds for “an exhaustive investigation into the possibility of foul play.”

“Jeff dedicated his life’s work to finding answers, always pushing the envelope, and never giving up, even at the risk of being perceived as controversial,” wrote his niece, Cali Bradstreet Howell, on the gofundme Web site. “Now, in this moment, we find ourselves in a position, where we too are in search for answers … and we intend on finding them.”

[Disneyland measles outbreak strikes in anti-vaccination hotbed of California]

Bradstreet had been a leading voice in the anti-vaccine, or “anti-vaxxer,” movement for nearly two decades.

He was a former preacher who traded the pulpit for a physician’s gown, according to the Gwinnett Daily Post. Bradstreet received his medical degree from the University of South Florida and completed his residency at the Wilford Hall USAF Medical Center in Texas, according to a paper he wrote.

His interest in autism was as much personal as professional. He made no secret about the fact that family had been touched by the disorder. “Both [my] son and stepson have autism spectrum disorders and have experienced significant recovery as a result of intensive biomedical interventions,” he claimed.

On his blog, Bradstreet detailed the painful story of how his own son’s struggles had pushed him to study autism — and increasingly controversial therapies.

“It takes a lot of courage to face the world with autism,” he wrote in a 2012 birthday letter to his autistic son:

From an easy pregnancy and simple delivery you progressed as a sweet and happy baby boy right up until 8 months when that first ear infection struck. It didn’t want to go away easily and ultimately you needed tubes to drain the infection. Prior to that we tried a lot of antibiotics and none worked. We didn’t realize back then that you had a primary immune deficiency and couldn’t make enough IgM to defend your body.

I can’t even talk about the next year and all the things that happened. But your mother and I had to watch our precious boy change without understanding what was happening. The first time you pulled the pans out of the kitchen cabinets and banged on them it was cute. The next 20 times it was obvious something was wrong. And then you just didn’t seem to cry when you fell and hurt yourself. I had never seen that before.

The worst part of those early years was the horrific diarrhea that would actually burn your bottom within seconds. That was so sad and so hard to treat. Back in those days we understood so little about the gut connection to autism.

Ultimately, secretin ( a simple hormone) give IV made a huge difference in that problem. It was an immediate change and even got you the attention of Bernie Rimland and the National Enquirer. Your response to secretin made you an immediate hit with about 10 million readers of the Enquirer and neither your nor my life has been the same since.

But as the National Enquirer coverage suggests, some of these treatments were salacious but scientifically iffy. (A 2012 study, for instance, found “no evidence that single or multiple dose intravenous secretin is effective” for treating autism.) Bradstreet also wrote about including his son in an intravenous immunogloblin (IVIG) trial that “made a huge difference.” But another study found IVIG only helped 10 percent of patients and “should be undertaken only with great caution.”

Nonetheless, his son’s case helped convince Bradstreet that vaccines caused autism. He took his message to the highest levels of government. Twice he testified about the supposed link between vaccines and autism before the U.S. House of Representatives.

“He was a very happy, well connected child prior to his MMR at approximately 12 months of age,” Bradstreet told representatives in 2002, presenting copies of his son’s various tests. “Matthew completely lost about 2 months after his MMR vaccine.”

From his clinic in Buford, Ga., Bradstreet treated patients from around the world, many who sought him out online. Desperate parents seeking answers for their children’s maladies would write to him on his blog, begging him for help.

But leading autism experts say Bradstreet was simply wrong, and that the autism therapies he espoused were “dangerous.”

“There is no evidence that vaccines cause autism,” Peter Jay Hotez, dean for the National School of Tropical Medicine at Baylor College of Medicine, told The Washington Post. “It is pseudoscience based on a misunderstanding of the whole neurobiology of autism.

“But there are a lot of worrying conspiracy theorists that keep on making up allegations about vaccines,” he said. “Every five years, the main variables change. I’ve seen about six iterations of this. As soon as one pseudoscience theory is debunked, someone comes up with something new.”

Hotez, who also has a child with autism, said it was understandable that Bradstreet and others sought answers to the still somewhat mysterious disorder.

“If you Google something on the Web, you can get a quick and easy fix,” he said. “Unfortunately that’s what a lot of parents do, and there is a lot of garbage on the Internet.”

Bradstreet’s beliefs were doubly dangerous, Hotez said. Not only did they scare people off of vaccines — something that has led to a resurgence of measles in the U.S. — but the treatments themselves can also be deadly.

[The devastating impact of vaccine deniers, in one measles chart]

“Bradstreet was promoting chelation therapy, which is dangerous and without any benefit,” Hotez said. Chelation involves the use of chemicals to remove metals from a patient’s blood.

The U.S. Food and Drug Administration says chelation can be used in cases of acute poisoning, but Bradstreet believed the procedure could treat autism by removing mercury — supposedly introduced by vaccines — from an autistic person’s blood.

The FDA, however, has warned against such “chelation therapies” for autism: “Chelating important minerals needed by the body can lead to serious and life-threatening outcomes.”

“Chelation therapy never made any sense from a scientific standpoint,” Hotez added. “So in the zeal to chelate mercury, which, again, there is no basis showing [it is the problem], Bradstreet would also chelate the calcium, and that would cause a very toxic reaction.”

“Chelation is certainly not appropriate” for treating autism, Michael Katz, a senior adviser to the March of Dimes and professor emeritus at Columbia University, told The Washington Post. He added that numerous studies have debunked the link between mercury in vaccines and autism, rendering chelation pointless.

Bradstreet was also a believer in hyperbaric oxygen chambers and stem cell therapy for the autistic.

It is unclear what role Bradstreet’s controversial research and therapeutic techniques might have played in his death. According to the Gwinnett Daily Post, the FDA and Georgia’s Drugs and Narcotics Agency raided his Buford clinic in the days before his death.

“Multiple law enforcement officials said the U.S. Food and Drug Administration searched Bradstreet Wellness Center last week,” the newspaper reported on June 26. “On Monday, [June 22] plastic sheets covered the windows of the two suites the office takes up in a complex off Commerce Drive, and the doors were locked. ”

It’s still unclear why the raid was carried out. For many, however, the timing seemed to fit with the official explanation of a suicide. Bradstreet’s body was found near where he and his wife vacation, the Daily Post reported. And, although less frequent than bullets to the head, suicide shots to the chest are not uncommon.

But Bradstreet’s family and broad network of supporters see a nefarious scheme in the series of events leading to his death.

“He was a fighter and would never just quit,” Bradstreet’s former wife, Lori, wrote on the gofundme Web site. “What we were told happened really does defy all reason. Thank you for all your help to find the truth.”

The Bradstreet family did not respond to multiple requests for comment.

“I can not accept the notion that Jeff would take his own life,” wrote former colleague, John Reinhold Sr. “His research was a threat to many representing huge financial losses in the hundreds of billions, if the direction his research was validating came to be accepted as ‘fact.’ We discussed this many times when he was in the earliest stages of his work. The public is unaware of how easy it is for someone knowledgeable whose financial interests are threatened to make a phone call and simply state, ‘He’s an annoyance we don’t need right now,’ and that simple statement putting plans in motion. If Jeff’s strong suspicions are right regarding cause and causes of autism, legal actions against those corporations implicated would be staggering and possibly unprecedented in the history of world finance. Jeff was brilliant and had every reason to live. Although we’ve not been in touch in recent years I can not fathom that he checked himself out.”

Others expressed their thanks for the miracles that Bradstreet had allegedly worked upon their autistic children, while quickly decrying his “murder.”

“I will always remember how helpful his office in Melbourne Fl. was to my very ill autistic child,” Marla Peters wrote. “My daughter is now 19, she was 5 when we first went to his office. No one would help her with her gut pain but this group of Dr.s helped her and myself. Forever grateful and sad because his work was not done! May God have vengeance quickly on the evil doers who murdered him!”

“One of the best doctors my son had in 21 years,” echoed Andrea Parker. “He did not kill himself! I simply don’t believe it at all. He was super religious and had an Autistic son himself. This looks really dirty to me.”

Hotez said passions run high in the autism debate. He and his family have received angry messages and e-mails but never death threats, he said.

And while he couldn’t comment about Bradstreet’s death, Hotez wondered if the homicide theories were, like vaccine conspiracies, half baked.

“There is a deep seated paranoia” in the anti-vaccine movement, he said. “There is a deep seated feeling that there must be something bad out there.

Commentary:  This Washington Post article is not journalism.  It is transparent where the writer is taking the reader and the story is filled with the words and phrases that do the job, namely, “dangerous,” “radical, ” “crackpot,” “ignored science,” “championed dangerous, discredited and occasionally deadly treatments,” “sees a slow downward slide towards suicide,” “the wound appears to have been self-inflicted,” “pushed him to study autism — and increasingly controversial therapies,” “scientifically iffy,” “although less frequent than bullets to the head, suicide shots to the chest are not uncommon,” “Hotez wondered if the homicide theories were, like vaccine conspiracies, half baked,” “There is a deep seated paranoia” in the anti-vaccine movement, he said.”  Accordingly, at the beginning and the end of the article, the bias embedded.  And the writer had found what sounds to be a ringer.  But if the article was absent recognizable journalistic standards, Michael Miller’s follow-up article was what the clique surely ordered, namely, the attempted coup de grace.  Please take the time to read the follow-up article and notice the very different style of writing, starting with inserting bias in the title of the story.  And, of course, the elephant in the room is that in both articles, there is no mention of the rising death count and disappearances of Dr. Bradstreet’s medical associates who were working with him.

The mysterious death of a doctor who peddled autism ‘cures’ to thousands

July 16, 2015

___________________________________________

By Michael E. Miller    Martin Baron, Executive Editor

James Jeffrey Bradstreet was one of the world’s most famous — or infamous — physicians. He believed vaccines caused autism. He even testified so before Congress. Twice.

But he didn’t just rail against Big Pharma. He also tried to beat it.

Bradstreet offered thousands of autism patients around the globe controversial treatments. He claimed he could effectively cure kids of their autism, cancer and other maladies simply by injecting them with protein shots.

When Bradstreet’s body was found last month in the Rocky Broad River in mountainous North Carolina with a bullet wound to the chest, therefore, friends, family members and patients pointed fingers at drug corporations. The FDA. Anyone but Bradstreet.

“He did not kill himself!” one patient’s parent wrote online.

“May God have vengeance quickly on the evil doers who murdered him!” wrote another.

Although the local sheriff said it was suicide, Bradstreet’s relatives quickly raised $33,000 online for “an exhaustive investigation into the possibility of foul play.” And on Tuesday, the family’s attorney announced that the money had been used to hire multiple private detectives who would investigate whether Bradstreet had, in fact, been murdered.

[Anti-vaccine doctor behind ‘dangerous’ autism therapy found dead. Family cries foul.]

Since his death, however, the conspiracy theories have begun to crumble as evidence has emerged linking Bradstreet to a shadowy online industry in unapproved medicine.

Bradstreet’s Internet postings tie him to an unlicensed medical factory that was recently shut down for producing potentially contaminated vials of a supposed wonder “cure” called GcMAF.

The day before his death, Bradstreet’s own clinic was raided by federal and state authorities searching for the same untested and unapproved “cure.”

And on the very day of his death, Swiss media reported that a clinic linked to Bradstreet had also been raided after five patients receiving GcMAF died.

As this international medical gray market began to unravel, so, too, did Bradstreet’s life.

Everything you need to know about the vaccine debate(1:34)

Here are some of the most common arguments for and against vaccination. (The Washington Post)

If any doubt remains about whether Bradstreet committed suicide, one thing is now abundantly clear: The controversial doctor’s questionable treatments had finally caught up with him.

A doctor’s ties to the online international gray market of unapproved drugs

Bradstreet was both beloved and belittled.

To his patients, he was a savior willing to try out treatments few others would touch. But to critics — including other doctors and autism advocates — he was a crackpot whose supposed cures could be more dangerous than the disorders themselves.

Despite scientific consensus to the contrary, Bradstreet believed vaccines could cause autism. And he recommended unorthodox and often unapproved autism treatments including hyperbaric oxygen chambers; hormone injections; stem cell therapy and chelation, a risky chemical procedure Bradstreet believed could remove the mercury supposedly introduced by vaccines.

But perhaps Bradstreet’s most controversial treatment was something called Globulin component Macrophage Activating Factor, or GcMAF. A protein that naturally occurs in healthy human blood, GcMAF can be removed, concentrated and injected into a sick patient.

During the past decade, a handful of doctors have claimed that GcMAF can cure anything from cancer to autism by boosting the human immune system.

Bradstreet was an avid believer. In posts on his blog — deleted but still cached online — he shared his GcMAF patients’ anecdotes. And in 2012, he gave a presentation in England in which he described giving GcMAF injections to 40 autistic patients ranging from 16 months to 21 years in age.

“It’s extremely potent in terms of its ability to work for children,” he announced. “Many from this [experiment] have gone on to basically lose the label of autism. They don’t have autistic distinctions any more after sometimes as little as 20 weeks of therapy.”

It was an incredible claim: a cure for one of the world’s most vexing disorders after just five months of injections.

During his speech, Bradstreet cited doctors studying GcMAF in Japan and Italy. He said that a paper on his experiment was being peer reviewed. And he name-dropped David Noakes, the head of Immuno Biotech, a company manufacturing GcMAF.

(He also announced a 25 percent discount on GcMAF for those in attendance.)

What he did not disclose, however, was that much of the research he cited had already been discredited and retracted; the journal considering Bradstreet’s paper was the scientific equivalent of self-publishing, and Bradstreet had close ties to Noakes and Immuno Biotech.

During the same U.K. trip, Bradstreet and Noakes made what was essentially a promotional video for Immuno Biotech and its brand of GcMAF, called First Immune.

“I’m here with Dr. Jeffrey Bradstreet from the U.S.A., the autism expert in the First Immune GcMAF laboratories,” Noakes said on camera. “Dr. Bradstreet has been using our GcMAF for 18 months and we’d like to thank you for, I think you’ve treated 900 children now?”

“Not just children,” Bradstreet boasted. “So the spectrum of my patients with autism ranges from somewhere around 18 months to goodness, somewhere around close to 40. So we’ve treated many adults with autism as well as chronic fatigue patients, cancer patients. So we’ve found application for a fairly broad number of disorders for the product.”

The two traded compliments for four minutes straight.

“We have been astounded in the time you have been here just how much biomedical science you know,” Noakes told Bradstreet. “We have never met a doctor with such an understanding at the microbiological level of how autism and cancer and other diseases work, and we are absolutely delighted to have you with us. And we look forward to what we know are going to be further breakthroughs in autism in the future.”

Bradstreet responded by saying Noakes had “state of the art equipment.”

“I think you have a fabulous team of good scientists who are doing some incredible work here to produce the highest quality of both effective activity as well as purity and sterility of product,” the doctor said. “It’s something I’ve been able to rely on now for close to two years. And it’s really wonderful to be able to a part of it.”

Then he made a pitch for why GcMAF was the perfect autism treatment.

“The wonderful thing about your product is that it’s really not me treating you,” he said. “It’s not like you come to my office and I have to dose you up with this medicine because this is something that parents can do in their home.

“It’s accessible to anybody around the world. Through your Internet sites you’ve made it available very broadly. We’ve used it in South Africa, China, India, Eastern Europe, South America and all over. So that’s been a wonderful experience to see parents have access to a therapy.

“… We are seeing some extraordinary results.”

For desperate parents: Google, order and inject

The U.S. Food and Drug Administration is clear: GcMAF is not a recognized treatment for autism.

“GcMAF treatments are considered investigational, and none are approved or licensed for use by the FDA in the U.S.,” the agency said in a statement sent to The Washington Post.

Nearly all doctors agree.

“Given there is no evidence that modulating the immune system would have any benefit for children with autism spectrum disorder – especially given ASD’s genetic or epigenetic basis – I am not sure why Dr. Bradstreet would want to use this for ASD,” Peter Jay Hotez, dean of Baylor’s National School of Tropical Medicine, told The Post in an e-mail.

It’s not even clear if GcMAF injections are safe. An initial “safety study” — the first of its kind — is still trying to recruit participants.

So why are thousands of people around the world ordering it online and injecting their kids with it?

Part of the answer lies in Bradstreet and Noakes’s incredible promises.

“Dr. Jeffrey Bradstreet has now treated over 2,000 autistic children with GcMAF and the results are well established,” according to one of Noakes’s Web sites. “85% improve, if only a little, and of them 15% have their autism eradicated. In all 3,000 children have been treated with GcMAF with similar results.”

Internet chatrooms reveal how desperate parents were drawn to these promises like moths to a flame.

The discussion forum on Autism Web shows hundreds of parents of autistic children seeking out alternative methods of treating, or even “curing,” their kids.

“We are doing GcMAF injections through Bradstreet,” began one thread in August of 2011. “It has been 5 weeks. Each shot is $90 so I’m hoping we will see something big soon. I would love to hear from anyone else that has been doing the treatment for longer than us.”

Dozens responded. The replies varied from wary to ecstatic.

“I’ve been reading about GcMAF on other boards but hadn’t realized that this treatment was already available,” one person wrote. “Have you seen any benefits/negatives yet?”

“I am skeptical about it as it is a pretty new treatment,” wrote another. “Have there been any long-term follow up patients who used it? … Is it okay to start it? What areas have improved in your kid? What is the source of the GcMAF? Is it human?”

A few had concerns specifically about Bradstreet.

“Dr. Bradstreet is going to Kiev, Ukraine?” one person wrote in response to a blog by Bradstreet promoting a trip to see “experienced experts” in the Eastern European country. “The clinic there looks like it should be in a horror movie, I would never go there!!!”

But if a few parents worried about exposing their kids to GcMAF, many more jumped at the opportunity to try out the supposedly wondrous protein on their struggling children.

Some seemed well aware that GcMAF was not an approved medicine.

“Getting homeopathic practitioner to put her name to the request for the test £20 (don’t think GP [general practitioner] would do this,” one wrote.

“I did go to my GP today and she had no idea what [the GcMAF test] was, but said they wouldn’t do it,” another wrote. “So looks like I now need to find someone just to help me get the test done, very frustrating.”

“Have you considered trying to get your child in to see Dr. Bradstreet?” someone suggested.

Many commenters credited Bradstreet and his First Immune GcMAF injections with perceived improvements in their kids’ health. They ranged from “small positives” to allegedly major breakthroughs.

“I was crying tears of joy last night as we put him to bed because he was talking more than ever before,” one wrote.

“Oooh! Autism schmautism!!!” a Bradstreet customer in South Africa victoriously announced after supposedly seeing their child’s symptoms melt away.

In contrast, however, several commenters described giving their kids months of expensive shots only to end up disillusioned with both Bradstreet and GcMAF.

“We have completed 20 shots of GcMAF so far. I am still waiting for the wow that everyone talks about,” one person wrote. Even worse, they described side effects including “crying and pains in his chest and stomach at least for first 3 days after the shot.”

“We are doing GcMAF injections. I have not seen any gains at all,” another person wrote. “I have seen the worse behaviors and tantrums. So after spending $1,300 for no gains and living in hell I am done with this.”

Others described nasty viral or bacterial infections which flared up after starting their kids on GcMAF.

“It came to a point where we couldn’t tolerate it any more,” an angry parent wrote.

Hotez, who has a child with autism, told The Post that because autism doesn’t have a known cure, many parents are driven to extremes to help their kids.

“If you Google something on the Web, you can get a quick and easy fix,” he said. “Unfortunately that’s what a lot of parents do, and there is a lot of garbage on the Internet.”

In the case of GcMAF, that garbage would ultimately prove dangerous for both patients and provider.

Five deaths, three raids and a suicide

Fiona O’Leary is a far cry from a fearsome detective. She is a thin, pale Irish woman with dyed crimson hair and Asperger’s.

But she also has two sons with autism.

So like Bradstreet’s patients, O’Leary began scouring the Internet for ways to help her kids. Instead, she found GcMAF, which she calls a “dangerous and unethical scam.”

“GcMAF is another dangerous unauthorized, unproven and very expensive treatment being used in the Autism field,” O’Leary told The Post in an e-mail. She is the founder of Autistic Rights Together, an organization that exposes bogus autism magic bullets. “Those offering this treatment are untrained and not medical Doctors,” she said of GcMAF. (Bradstreet, it should be noted, was licensed to practice medicine in Georgia at the time of his death.)

O’Leary began investigating Bradstreet, Noakes, Immuno Biotech and their GcMAF solution, First Immune, in 2014. She began with First Immune’s headquarters in Guernsey, one of the Channel Islands.

Her complaints led regulators on the island to raise concerns in December with the Medicine and Healthcare Products Regulatory Agency (MHRA), the United Kingdom’s version of the FDA.

In early February of this year, the MHRA launched a raid of the First Immune GcMAF production facility near Cambridge — the same lab where Bradstreet had obtained his injections and had filmed promotional videos.

But where Bradstreet had seen a “sterile” and “state of the art” laboratory, the British government saw a nightmare.

MHRA investigators announced that they were shutting down the “unregistered” and “unlicensed” pharmacy after finding that the GcMAF was being made with blood plasma labeled “Not to be administered to humans or used in any drug products.”

“The production site does not meet Good Manufacturing Practice (GMP) standards and there are concerns over the sterility of the medicine being produced and the equipment being used,” MHRA said in a statement. “There are concerns that the product may be contaminated.”

“These products may pose a significant risk to people’s health. Not only were the manufacturing conditions unacceptable but the originating material was not suitable for human use,” said MHRA Director of Inspection Gerald Heddell. “GcMAF products labelled as ‘First Immune’ are not licensed medicines and have not been tested for quality, safety or effectiveness. People should not start treatment with these specific products. It is important that patients currently taking these products seek their doctor’s advice as soon as possible.

“The advice is, do not buy medicines online from an unregistered pharmacy as you don’t know what you are getting, where it came from or if it’s safe to take,” he said.

But the GcMAF saga didn’t end there. O’Leary was hounding American officials as well. After spotting Bradstreet’s videos and blog posts mentioning his connections to Noakes and First Immune, O’Leary complained to the FDA about the American doctor.

Four months after First Immune was shut down, the feds came knocking on Bradstreet’s Buford, Ga., clinic.

A search warrant dated June 16 and obtained by The Washington Post shows that authorities were explicitly looking for GcMAF, as well as other “misbranded drugs.”

The raid took place on June 18, the day before Bradstreet died, Noakes told The Post in a phone interview. Agents from the FDA and the Georgia Drugs and Narcotics Agency confiscated vials of GcMAF, medical records, lists of clients and associated companies, computers and financial records, according to the search warrant.

Had he been indicted, Bradstreet would have faced up to 20 years in prison, according to Forbes, which first obtained the search warrant.

The doctor left town. He packed his suitcases and drove three hours northeast across state lines to North Carolina.

But as he checked into a hotel near Lake Lure, N.C., the next day, more bad news was breaking for Bradstreet.

In Switzerland, three newspapers reported that very morning that a First Immune clinic run by Noakes had been shut down. Five patients being treated with GcMAF had died, the papers reported. Some had been spending up to 6,000 euros (about $6,500) a week for their treatment.

“Private clinic under criminal investigation after five deaths,” ran the headline in newspaper 24 Heures.

“We have reported the deaths of patients treated at the University Hospital in Bussigny,” said Darcy Christen, a spokesman for the local hospital. “We did it after discovering a body of consistent evidence that show questionable practices.”

“We found these situations serious enough to try to understand what was happening in Bussigny because the First Immune clinic is not officially registered in Switzerland,” said Karim Boubaker, a local government health official. “For us, it therefore does not exist and we were not sure what was happening. In addition, GcMAF is not allowed in Switzerland.”

Calling the clinic “an illegal practice of medicine,” Swiss officials launched an investigation into First Immune. (It’s still unclear if the deaths had anything to do with GcMAF or if the injections simply failed to help terminal patients.)

It’s impossible to know how the bad news affected Bradstreet, but it definitely came just hours before his death. When he arrived to his hotel in North Carolina on June 19, the room wasn’t ready, according to the Atlanta-Journal Constitution. Instead of waiting, he left — never to return.

Bradstreet’s body was found by a fisherman that afternoon. The gun that was used to kill him was found nearby in the water, according to authorities.

The Rutherford County Sheriff’s Office wasted no time in ruling the death a suicide.

“Everything is what it appears to be,” Lt. Jamie Keever, the lead detective on the case, told the Atlanta Journal-Constitution. “It’s a self-inflicted gunshot wound to the chest.”

Authorities are still waiting on an autopsy but the forensics and circumstantial evidence both suggest suicide. After all: The feds were onto him. His GcMAF supplier had been shut down. The wonder “cure” had been linked to five deaths in lurid headlines. Bradstreet’s life and profession were falling apart.

The shadowy international trade in unapproved medicine that had provided Bradstreet with so much business was finally coming to light.

But Bradstreet’s friends, family and patients have refused to believe the doctor killed himself. None is more skeptical that David Noakes.

“I know it was murder,” the Immuno Biotech CEO said. “Dr. Bradstreet stated what we all know: that the MMR vaccine causes autism,” repeating a claim often wielded by anti-vaccine activists that’s been totally debunked. “And he was an expert witness in many court cases in the U.S.A. providing testimony to that effect. MMR is a multibillion dollar vaccine and this [GcMFA] hurts the profits of the MMR drug companies and that is why he was killed.”

In a half-hour phone interview, Noakes told The Post that he was convinced a vaccine company killed Bradstreet to protect its profits from the wonder “cure” that is GcMFA.

“He was raided by the FDA the day before his murder so the murder is now dressed up to look like suicide,” Noakes claimed.

“Why would a doctor use a gun?” he continued. “A doctor wouldn’t use a gun at all. He’d use barbiturates or a cocktail of drugs which are easily available to him and take no effort.”

Noakes went on to defend his friend, who he admitted he had supplied with GcMAF.

“Before he was killed, he was recovering 60 percent of autistic children using GcMAF,” Noakes said of Bradstreet. “That is the highest recovery rate in autism in the world by far.”

Noakes went on to claim that both the MHRA and FDA were in cahoots with vaccine companies to bury GcMAF and the men providing it. He accused MHRA of “absurd lies,” “pure fraud” and “corruption” in shutting down his U.K. facility.

And although he admitted that a rash of GcMAF patients had died at his Swiss clinic before it, too, was shut down, Noakes said that the media had buried the real story: the clinic’s success.

“We had 76 terminal stage four cancer patients,” he said. “We saved 70 percent of them. They went home improving. The other 30 percent of them died but all 100 percent of them were expected to die.”

“They were prosecuting us for manslaughter to start out off with. They have now given that up because they realized how ridiculous that is in a terminal stage four cancer clinic,” he said, adding that his clinic was instead currently facing fraud charges.

Noakes admitted to using substances “not to be administered to humans” in his GcMAF but insisted that was common practice and that his product was safe and sterile. He also boasted to sending his vials to 9,000 patients in 80 nations.

Ensuring that his company’s medicines abide by international law wasn’t his concern, he said. “If the regulators have so much time on their hands, let them do it,” he said smugly.

“We are residents in Guernsey. We only have to follow Guernsey law,” he added. “We can’t possibly be expected to know the law in every country. It’s up to the person who is purchasing it.”

“So I don’t think it’s us you need to be pointing fingers at,” he concluded. “It’s utterly corrupt regulators you need to be pointing at.”

Outlining a vast, global conspiracy to suppress GcMAF and discredit or even kill its proponents, Noakes said Bradstreet had paid for his beliefs with his life.

“He was an extremely confident man despite 10 years of threats,” he said. “Dr. Bradstreet was never embarrassed. He never had any doubts.”

Commentary:  This is exactly how the clique tries to maintain the high wall of false reality that surrounds us all.  But the clique is notorious for its lack of subtly and therefore, with any experience with “hit” pieces, the reader immediately knows what’s going on.  It remains to be seen if the clique can put the genie can be put back in the bottle.  In the meantime, here is a critique of the Washington Post’s editorial board’s transparent criminality from a well-respected source, Natural News.

Washington Post editorial board functions as quack science Monsanto operatives… key articles essentially ‘written’ by Monsanto… eat more GMO!

May 29 2015

Hold your laughter on this when you read the Washington Post’s explanation of why GMOs are safe. (It would earn them an “F” in high school science!) Their article claims “Men and women have been cross-breeding — genetically modifying — plants and animals since the dawn of agriculture.”

This hilariously ignorant science explanation is ripped from page one of Monsanto’s quack science trolling playbook. It intentionally conflates selective breeding with genetic engineering, deceitfully implying that they are biologically equivalent.

Selective breeding, of course, is a natural process where plants with the most desirable traits are chosen to pollinate the next generation of plants. This is how modern corn was developed over thousands of generations of breeding that began with grasses.

Any high school science student would earn an “F” if they answered the test question, “Explain genetic engineering” with the ludicrous answer offered by the Washington Post: It’s basically the same as selective breeding. The Washington Post’s editorial board, it seems, flunked out of basic science, and that unfortunate state of cognitive incompetency weaves its way through the paper’s science scribblings on a daily basis.

As any educated scientist knows, genetic engineering is the artificial alteration of the genetic code of a plant by inserting genes which often come from soil microbes, insects, or other life forms “alien” to that plant. Genetic engineering is artificial and fraught with potential danger because it is a self-replicating technology with unknown long-term consequences to the biosphere. GMOs are therefore a potential source of genetic pollution in addition to all the other risks they pose to consumers and the environment. Beyond that, GM crops are also giving rise to herbicide-resistant superweeds in exactly the same way that modern medicine’s abuse of antibiotics has given rise to superbugs.

None of these issues seems to bother the Washington Post. Its editorial board hilariously pretends none of these risks exist at all. What? Me worry? Heck, there are advertisers to please, even if it means the Post has to neuter its own journalistic integrity and trade credibility for cash. (C’mon, Bezos, fire those dolts already! Surely you can turn this paper around and restore it to something resembling honest news…)

Washington Post now 100% aligned with Monsanto’s agenda of widespread poison and deception

The Washington Post’s intentional conflating of selective breeding vs. genetic engineering is practically an open admission that their editorial board is blindly obedient to the agenda of Monsanto. The Post is the puppet, and Monsanto is the puppet master who tells them what to say. That’s how you end up with the Washington Post uttering hilarious biotech industry lies such as, “The promise of GMOs, already widely used in the United States, is that farmers in the developing world can use them, too, and thus feed their hungry populations at far lower cost than ever before.”

This explanation is, of course, another biotech industry talking point that no informed person who isn’t on Monsanto’s payroll really believes. In truth, GMO crops are failing like never before, and the promise that GMO agriculture would require less application of pesticides turned out to be completely false as well. Glyphosate, in particular, is now globally recognized by the World Health Organization as being linked to cancer, and more and more nations around the world are banning it outright.

Glyphosate is so toxic and dangerous to consumers that the German retailer REWE just banned glyphosate from all its stores. Similarly, the entire Dutch Parliament recently voted to ban glyphosate sales to individuals across the entire country.

GMOs and glyphosate go hand in hand, of course: You can’t have one without the other. The Washington Post, like every other group of biotech-corrupted trolls who pretend to be journalists, hilariously implies that glyphosate is safe — largely because Monsanto told them so! Who needs REAL science when you’ve got paid “corporate science” instead?

When the Post’s arguments begin to resemble the same talking points of people like Jon Entine — a paid biotech troll and character assassin who was exhaustively exposed by Natural News — you know the Post’s credibility has been totally abandoned.

Jon Entine, who was fired by Forbes.com after being exposed by Natural News, is a violent wife abuser, according to these court documents, who routinely fabricated false “facts” and got them printed on Forbes.com. (Forbes was later forced to retract at least one article that was filled was utterly fabricated accusations against Natural News. Heck, even Forbes, which is also beholden to Monsanto, couldn’t stomach the repeated lies of this guy who remains a research fellow at the American Enterprise Institute. Maybe Entine can get a new job writing GMO lies for the Washington Post!)

The media strategy behind all this is to try to intimidate restaurant chains into keeping GMOs on their menu (and thereby poisoning their own customers while enriching Monsanto). As ANH-USA writes:

Rather than adding anything meaningful to the debate, the major media outlets are sending a clear message to the restaurant industry: “If you follow in Chipotle’s footsteps, we will make an example of you.” It seems clear to us that such a frontal attack by major news outlets must have been instigated by the biotech industry’s PR departments.

Trust in mainstream media collapsing by the day

Then again, all this probably doesn’t come as a surprise to anyone. We live in an era when the mainstream media is almost universally perceived as an institution of corporate-funded professional liars. That’s why public trust in the lying mainstream media is plummeting by the day. Thanks to revelations about Brian Williams (NBC’s liar-in-chief) and George Stephanopoulos (ABC’s liar-in-chief), everybody now knows that all the big mainstream media outlets are run by compromised liars and political operatives who twist the news to appease their egos, their advertisers, or their political controllers.

The Washington Post is the classic example of this. Its science editors are so incredibly compromised by industry influence that they can’t get their heads around this logic conundrum: If vaccines confer immunity, then vaccinated children have nothing to fear from unvaccinated children. Therefore, unvaccinated children pose no risk to vaccinated children… unless we’ve been lied to about how well vaccines work, of course.

You won’t find a single Washington Post science editor who can exercise anything resembling real logic on issues like GMOs and vaccines. Instead, they express what can only be called “zombie logic” — the mindless obedience to official sources while invoking ridiculous twisted justifications for the continued mass poisoning of the people with glyphosate and mercury in vaccines. See my article Irrefutable proof that influenza vaccines routinely given to pregnant women still contain mercury.

All this makes me wonder: Has the Washington Post ever met a toxic chemical it didn’t like? The paper is pro-fluoride, pro-mercury in vaccines, pro-glyphosate, pro-GMOs, pro-chemotherapy, pro-pesticide, pro-herbicide and pro-Big Government. Maybe instead of “Washington Post,” the paper should rename itself the “Corporate Greenwashington Post.”

Looking for REAL, independent science? See the Natural News labs

If you’re looking for real, independent science on food safety, look no further than the site you’re reading right now, Natural News. Here, we operate the only ICP-MS food science lab in the world that’s owned by a media organization. As the science lab director, here’s some of what I’ve managed to accomplish in just the last 18 months as an independent science researcher with zero financial ties to Monsanto:

* Running an ICP-MS science lab, with ISO 17025 accreditation pending.

* Was the first scientist in the world to document tungsten contamination of brown rice protein.

* Was the first scientist in the world to document the lead and cadmium contamination of brown rice protein and achieve the world’s first industry agreement to reduce those contaminants.

* Invented and patented (pending) the world’s first cesium-binding dietary supplement that can protect lives during nuclear disasters by blocking the body’s absorption of radioactive isotopes of cesium-137.

* Developed and documented a Heavy Metals Defense supplement that binds with toxic heavy metals using ion exchange technology in a safe dietary ingredient.

* Developed the Food Rising Mini-Farm Grow Box and gave away 250 of these units to schools all across America to teach children how to grow their own food. (See some photos here.) Personally invented the 3D-printable parts for this revolutionary home food production system and gave them away to the world for free. Click here for the downloadable, 3D-printable parts I developed and released to the world for free.)

* Have invented the world’s first 3D-printable device that removes arsenic from contaminated well water. I’ll be giving away this invention to the entire world for free, via FoodRising.org.

* Independently tested and verified the heavy metals removal capabilities of off-the-shelf water filters. Results are published now at www.WaterFilterLabs.com

If the Washington Post had any interest at all in independent food science, they would be contacting me for laboratory assistance, not attacking Chipotle and its fans. But as we’ve already established, the Post isn’t interested in real science. It’s far more important for the paper to protect the financial interests of its corporate advertisers.

The sad thing is that I don’t believe the Washington Post’s obedience to Monsanto really reflects the intentions of Jeff Bezos, the new owner of the Post. Maybe it’s time for Bezos to knock some heads around and clean a little house. The Post, after all, could gradually restore its trust and credibility by apologizing to its readers, firing its scientifically illiterate editorial board, and reporting the truth about glyphosate, genetic pollution, seed monopolies and Monsanto’s nefarious and deceitful tactics.

I’m not holding my breath waiting around for that. Neither is anybody else, which is why they’re all rushing to the New Media / Independent Media to get their news these days.

Action item: Thank Chipotle for going non-GMO!