Doctors are Being Killed for Saving Your Children ~ Most Urgent!!!

 Subject: Vaccines, Dead Doctors, and Depopulation- If You Haven’t Seen This Video, You Should

           Ted Broer The Top 10 Foods Never to Eat (FAIR USE: Educational)

The GcMAF Book
Chapter 9

Nagalase: Friend and Foe?

What is Nagalase?

Nagalase is a protein made by all cancer cells and viruses (HIV, hepatitis B, hepatitis C, influenza, herpes, Epstein-Barr virus, and others). Its formal, official chemical name is alpha-N-acetylgalactosaminidase, but this is such a tongue-twisting mouthful of a moniker that we usually just call it “Nagalase.” (Sometimes, when I want to impress friends with my brilliance, I’ll say the entire word real fast: “alpha-N-acetylgalactosaminidase.” I have found that it’s important to practice beforehand if one doesn’t want to embarrass oneself.)

Why is Nagalase important?

1.    Nagalase causes immunodeficiency. Nagalase blocks production of GcMAF, thus preventing the immune system from doing its job. Without an active immune system, cancer and viral infections can grow unchecked.

2.    As an extremely sensitive marker for all cancers, Nagalase provides a powerful system for early detection.

3.    Serial Nagalase testing provides a reliable and accurate method for tracking the results of any therapeutic regimen for cancer, AIDS, or other chronic viral infection.

Nagalase proves that cancer cells break all the rules

Normal healthy cells cooperate with one another in a concerted effort to further the good of all. Cancer cells refuse to play ball. Their disdainful attitude toward the rest of our cellular community is appalling. For example, these cellular scofflaws ignore clear messages to stop growing and spreading and encroaching on their neighbor’s space. How would you like it if your neighbor moved his fence over into your backyard?

Of all the rules cancer cells break, none is more alarming than the production of Nagalase, the evil enzyme that completely hog-ties the immune system army’s ability to stop cancer cells.

Virus particles also make Nagalase. Their goal is the same as that of the cancer cells: survival by incapacitating their number one enemy: the immune system.

Nagalase precision

Like a stealth bomber, the Nagalase enzyme synthesized in and released from a cancer cell or a virus particle pinpoints the GcMAF production facilities on the surface of your T and B lymphocytes and then wipes them out with an incredibly precise bomb. How precise? Let me put it this way: Nagalase locates and attacks one specific two-electron bond located at, and only at, the 420th amino acid position on a huge protein molecule (DBP), 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 six thousand miles away. More astonishing, if that is possible, Nagalase never misses its target. There is no collateral damage.

As you already know, GcMAF is a cell-signaling glycoprotein that talks to macrophages, enabling them to rapidly find, attack, and kill viruses and cancer cells. By activating macrophages, GcMAF triggers a cascade that activates the entire immune system. Blockage of GcMAF production by Nagalase brings all this wonderful anti-cancer and anti-viral immune activity to a screeching halt, allowing cancer and infections to spread.

What does Nagalase actually do? How does it destroy immune functioning and deactivate macrophages?

Once synthesized and released into nearby tissue or into the bloodstream, Nagalase, like that drill sergeant at boot camp, shouts harsh commands at the vitamin D binding protein (DBP) that is about to be turned into GcMAF. Nagalase demands that DBP not, under any circumstances, attach itself to a specific sugar molecule (galactosamine). If DBP has already grabbed (i.e., connected to, using a two-electron, “covalent” bond) a galactosamine sugar molecule, it is commanded to immediately let go. “Leave galactosamine alone, or you’ll be in big trouble!!!” is the Nagalase sergeant’s command. We’ll probably never know whether or not, on some deeper level, DBP knows that Nagalase’s motives are dastardly—but it doesn’t really matter: DBP will definitely always obey. Like the army private, the DBP literally has no choice. Because of the way hierarchies work in cellular biology, proteins must do the bidding of their enzymes. The enzymes, like Nagalase, are the drill sergeant and the proteins, like DBP, are the privates. That’s just the way it is. Obeying the drill sergeant’s command means DBP can’t do its assigned task, that of becoming GcMAF. It is rendered useless. For DBP, on a molecular level, life no longer has meaning.

Unfortunately for cancer and viral patients, DBP had been on its way to becoming GcMAF until the Nagalase drill sergeant so rudely interrupted. Now GcMAF—the one protein our bodies need in order to activate our immune systems—can’t be made. Immune activity screeches to a halt. The defense system protecting us from cancers and viruses has been snuffed out.

Nagalase, using this astonishingly simple yet cunningly subversive technique, emasculates the GcMAF precursor protein (DBP) by knocking off its three sugar molecules. One quick whack by Nagalase and the DBP protein that would have become a GcMAF molecule now limps off into the sunset, permanently disfigured and disabled. With one simple, swift maneuver, Nagalase has brought the entire immune system to its knees.

Here’s how Dr. Yamamoto put it (for clarity, I’ve replaced some of the technical words):

“Serum vitamin D3-binding protein (DBP) is the precursor for the principal macrophage activating factor (GcMAF). The precursor activity of serum DBP was reduced… These patient sera contained alpha-N-acetylgalactosaminidase (Nagalase) that deglycosylates (removes the sugars from) DBP. Deglycosylated DBP cannot be converted to GcMAF, thus it loses the GcMAF precursor activity, leading to immunosuppression.” (Microbes Infect. 2005 Apr;7(4):674-81. Epub 2005 Mar 22. Pathogenic significance of alpha-N-acetylgalactosaminidase activity found in the hemagglutinin of influenza virus. Yamamoto N, Urade M.)

Nagalase testing: former mass murderer now works for the good guys

It’s easy to be a little schizy about Nagalase. On the one hand, this nasty protein’s behavior toward us has been reprehensible and disastrous. Working in cahoots with cancer and HIV—not shy about getting into bed with our mortal enemies—Nagalase can rightfully claim direct responsibility for billions of human deaths. And it would just as soon add you to the list, so we don’t have to be shy about placing Nagalase in the “genocidal murderer” column.

With the advent of Nagalase testing, however, this bad actor now will be harnessed to a useful purpose. By providing us with precise and reliable advance information about enemy operations, Nagalase blood level testing becomes a “Deep Throat” double agent for cancer. He helps us by giving us an early warning sign.

Early detection (using AMAS or Nagalase) saves lives

You don’t want a cancer to have gotten out of control by the time you find and start treating it. When cancers are still young and small, gentle natural therapies are the most effective. Alternative treatments work best on early small cancers by enhancing immune functioning and removing the source of the inflammation that is causing the cancer in the first place. Cancers that have become large enough to see on imaging pose a much more significant threat, and the big guns now become necessary.

The current method for diagnosing most cancers requires us to wait until a mass shows up on imaging (e.g., a mammogram, chest X-ray, or colonoscopy). This approach wastes valuable time and causes needless deaths. But long before imaging can find it, a positive Nagalase (or AMAS test) can tell us that early stage cancer exists somewhere in the body. By enabling earlier and therefore less invasive treatment options, this information provides a huge head-start.

Normally present at only trace levels, Nagalase shows up in the blood when a cancer or virus appears

The malignant and viral entities that make Nagalase are not normally present, so its appearance is a big deal from a diagnostic perspective. When Nagalase shows up, even in very small amounts, we have the earliest glimpse of a new cancer or viral infection. The old adage, “Where there’s smoke, there’s fire” applies here. A positive Nagalase test notifies us that a cancer (or a nasty virus) lurks within.

Nagalase appears in the blood stream when a nascent cancer is just a minute cluster of abnormal cells, long before conventional diagnostic methods can detect it. Through blood testing, we can find this red flag, even when present at exceedingly low levels. Providing us with this early warning sign might not quite qualify Nagalase for the “Good Samaritan” award, but I could go with “extremely useful.” Like a rehabilitated criminal on parole, the potential for harm is still there. For now, however, he’s staying out of trouble and doing community service. Turn your back and he’s a mass murderer again.

Using Nagalase testing to track cancer treatment

Rising Nagalase levels indicate a cancer or virus is growing and spreading. Conversely, Nagalase levels will decrease if the cancer or infection is being effectively destroyed.

Any treatment that lowers cancer cell (or viral numbers) will lower Nagalase levels. Nagalase will, for example, always drop after surgery (whether or not the entire tumor was removed). Chemotherapy and radiation also reduce Nagalase levels. So does GcMAF. If, after these treatments, the depressed level begins to rise again, this is the warning sign that the cancer was not completely removed, and/or that metastatic disease is hiding out somewhere. With viral infections, increasing Nagalase levels indicate return of the infection.

Consecutive rising Nagalase levels are therefore a red flag, warning us it may be time to entertain new treatment options. Conversely, if levels are going down, stay the course: the cancer or virus is going away.

Flat-earth medicine

Many medical professionals don’t feel comfortable with “nonspecific” tests like Nagalase. It drives them nuts to discover that a cancer is lurking somewhere inside without knowing exactly where it is located. “How,” they ask, “do you expect me to treat a cancer I can’t see? Why, I’m not going to tilt at windmills!” This may be a signal that you need to find a different doctor, perhaps one who works in an alternative cancer clinic. Here you will find highly-trained professionals who understand the concept that cancer is a molecular biological change long before it presents visually (by this I mean becomes viewable on imaging).

When GcMAF becomes available, the answer will be easier: a six month course of weekly 100 ng GcMAF intramuscular injections with monthly Nagalase level tests to follow the Nagalase level as it goes back down to baseline. The cancer can be declared cured, even though it never reached life-threatening proportions. (We have a long way to go before this kind of medical behavior will be commonplace and acceptable. The sooner the better, however.)

Nagalase role “under-appreciated”

Nagalase, arguably our most immunosuppressive protein molecule, poses an enormous threat in terms of cancer perpetuation and viruses’ ability to continually defeat us. Yet cancer researchers have not shown any interest in it. (Maybe I’m being a little too generous here; perhaps “clueless” would be more a more accurate depiction.) Why don’t they get it that blasting cancer cells into oblivion with chemo and radiation is usually not sufficient to stop advanced disease and does nothing to address the cause: immunosuppression. Even if we ignore for the moment the excessive collateral damage caused by chemo drugs and radiation, the patient also needs—requires—a healthy immune system to finish the job. If we don’t revive immune function by disabling Nagalase, the cancers and viruses will just keep roaring back. Restoring immunocompetence by negating the stultifying effect of Nagalase should therefore become a primary research goal.

 

Nov 22, 2015 - Dr. Ted Broer explains why doctors are being killed for what they've ...
 -of-what-they-have-discovered-about-vaccines-killing-our-children.html ...

 

Dr. Ted Broer explains why doctors are being killed for what they’ve discovering about vaccinations and how to cure the effects of the Elite’s genocide.forced on your children and those taking forced vaccinations.
The interview continues:https://www.youtube.com/watch?v=KH06d…
Full interview on Hagmann & Hagmann:https://www.youtube.com/watch?v=8g0NM… 

Via http://www.philosophers-stone.co.uk/

http://beforeitsnews.com/alternative/2015/11/doctors-being-killed-because-of-what-they-have-discovered-about-vaccines-killing-our-children-3246918.html

Dr. Ted Broer The Top 10 Foods Never to Eat (FAIR USE: Educational)

https://www.youtube.com/watch?v=jJwK7waQOF4

Do not touch

1.

2. Margarine

3. Shell fish that may be contaminated

4. Salami that has sodium nitrate in it

5. Sugar is addictive to the brain as cocaine.

 6. Junk food, twinkies, cup cakes…

7.

8. Milk and dairy products are not organic

9. Coffee Products –only occasionally

10. Daily use of alcohol ..occasional use only

11. GMO’s . which re-write4s your DNA in your body… Monsanto are now making allumimum resistant seeds

Chem Trails

2 inch rain water sample

Then has big chem trail spray, the it rained and took a sample

They had so much allumimum in the water it was unsafe to drink

 

5-7% of earth’s crust in alluminmum

But very hard to separate..

Alluminmum will cause dementure and alzheimers disease

 

Dr Ted Broer talks about toxic foods we eat - theDove.us

Published on Feb 6, 2014

 

Dr. Ted Broer, one of America's leading nutritionists and biochemists and author of "Breakthrough Health," talks about toxic foods we eat that eventually eat us.

https://www.youtube.com/watch?v=xmURP-M05Aw

 

 

One of America’s leading nutrients,

Dr. Ted Broer’s book, Break Through Health

 

Nagalase is the substance that cancer cells produce to stop the immune system killing cancer cells

 

Many of these doctors committed suicide or suddenly died.

GC Protein used by macro fages in the body that kill cancer cells.

You have to take vitamin D every single day.

GCMAF protein

Vitamin D binding protein

Single most effective thing in the immune system that can kill cancer cells

Nogales Protein compound has been introduced into the body and being added through the immunisation being given nagalase molecules and/or through viruses

GC protein cannot attach itself to the Vitamin D because of the Nogales…

This Nogales was not in these children at child birth and has been introduced into the body and being added through the immunisation being given nagalases molecule and/or through viruses

 

https://news.google.com/newspapers?nid=1798&dat=19730502&id=5_YeAAAAIBAJ&sjid=JY0EAAAAIBAJ&pg=7237,545317&hl=en

 

 

 

 

 

 

How Cancer Cells Spread : New York-

Sarasota Journal Wednesday, May 2, 1973- Page 4-B.

 

“…. most, if not all, cancer tissues contain the foreign substances called tumor-specific antigens. These are not found in normal, non-cancerous tissues in a person’s body….”

 

The blood serum of about 80 per cent of black people contains a substance which may help stop the growth of cancer in white patients when it is injected, according to a husband and wife team of cancer fighters in Seattle, Wash.

The “black factor” appears to unblock a mechanism in cancer patients which previously prevented the individual’s body from fighting off the invading cancer cells.

This theory stems from the work of Drs. Ingegerd and Karl Hellstorm over the past several years in which they have found clues to fighting cancer – the same system which rejects  a transplanted heart or other organ because the tissue is “foreign”.

Work of the two physician-researchers, originally from Sweden’s famed Caroline Institute is based on their findings – now confirmed by others – that most, if not all, cancer tissues contain the foreign substances called tumor-specific antigens. These are not found in normal, non-cancerous tissues in a person’s body.

Usually these foreign substances would cause a person’s system to produce antibodies, including certain types of white blood cells called lymphocytes, to fight them. But the mystery has been in the body’s apparent lack of ability to knock out a cancerous growth in this way. The Hellstroms have found that the blood of laboratory animals and many cancer patients does contain antibodies that are capable of killing off the cancer which their bodies harbour. And these antibodies do kill cancer cells in test tubes in the laboratory – but not in the patient’s body.

This is due to a substance called “blocking anti-body,” which the Hellstroms have discovered. It appears to protect a cancerous tumor from attack by the body’s lymphocytes.

It is this blocking anti-body which the black factor seems to destroy. In studies, the Helstroms repeatedly found that serum from certain donors seemed to unblock the blocking antibody in tumor cells taken from more than 100 patients with a relatively rare type of cancer called melanoma. In other words, serum containing the “black factor” enabled the bodies of melanoma victims to more effectively fight off their cancers on their own.

“We soon noticed that we started to recognize some of the names of the serum donors. They were black people who were working with us, or students and technicians,” explained Dr. Karl Hellstrom in a recent interview in Nogales, Ariz., where the American Cancer Society held its annual seminar for science journalists.

“We then did a systematic study of blacks and whites and found that whites react immunologically to melanomas about five per cent of the time, but blacks reacted at about the frequency of 80 per cent.”

As one would therefore expect, melanomas are exceedingly rare in the black population. And when they do occur they are usually on the palms of the hands or the soles of the feet – areas where there is much less skin pigmentation.

The Hellstroms stress that their studies are strictly at an experimental stage. They are currently conducting a project with six melanoma patients who have failed to respond to conventional methods. This study will be broadened to 60 patients in the next two years. These patients will receive transfusions of blood from healthy black donors in an attempt to determine scientifically whether they can recover better than patients receiving plasma from while donors.

The researchers said they “felt encouraged” about their work, and added that if their experiments do indeed indicate that serum from blacks does help certain cancer patients, it would be possible to treat both potential and actual victims.

“Potential” victims of this and other types of cancers may be detected while the tumors are exceedingly small, and thus much easier to treat, if another part of the Hellstroms’ research develops.

Basically, they have discovered that the “blocking antibodies” can be found in a patient’s blood serum before a tumor can be detected by any other means. At this time, however, such tests are extremely complicated. “Before anything else, the strategy should be to simplify the very complicated techniques which we are using,” DR. Karl Hellstrom said.

Although the Hellstroms believe that this type of test looks promising, they note that their studies thus fat have been small and much broader studies are needed to think about mass screenings of the public.

The Hellstroms’s findings suggest that if physicians can improve a patient’s anti-tumor reactions without increasing the blocking antibodies, or if the blocking antibodies, or if the blocking antibody’s effect can be decreased without affecting anti-tumor activity, there will be therapeutic benefits for many patients.

 

“BLACK FACTOR”  - Drs Karl and Ingegerd Hellstrom have discovered a “black factor” which comes from the serum of black persons and may help cure some forms of cancer in whites.

 

 

 

How Cancer Cells Spread .

news.google.com/newspapers?nid=1798&dat=19730502&id...

... which they have found clues to fighting cancer in the body's immune system the ... Usually these foreign substances would cause a person's system to produce ... And these antibodies do kill cancer, cells in test tubes in the laboratory— but ... a recent interview in Nogales, Ariz., he American Cancer Society held its annual ...

 

Dr Tim Smith MD

Naglase is like a stealth bomber

Locates and attacks in a very selective and precise way…

Like taking out a park bench in Central Park with co collateral damage..

Children has very high levels of

GCMAF

Vitamin D binding macro fages

Chronic fatigue, autism, parkinson, alzheimer disease had an  85% positive response rate as result of treatment with GCMAF

 

And 15% complete cure of

Strong anti-cancer effects

Of kidney, prostrate etc cancers

 

Autism has now skyrocketed to ONE IN 45 in this country. That means if you walked down your street right now, it’s highly likely you wouldn’t even have to go a full block before you will have passed a home with at least one autistic child living in it. What you are about to hear may be why.

When the CDC Whistleblower story broke in the fall of 2014, the Establishment quickly went to work to black it out and cover it up. Regardless, it’s on record that a government epidemiologist admitted he and his cohorts massaged and omitted data in a study to hide a huge increase in autism following MMR vaccination. He then promptly lawyered up with one of the most high profile whistleblower attorneys money can buy in this country and issued a statement. Then the whole thing got swept under the rug in what appears to be a purposefully overblown ebola scare and forgotten by many.

Fast forward to last summer, when a bunch of doctors began turning up dead around the country under mysterious circumstances. Some twelve doctors died within three months and many were found under suspicious circumstances (such as randomly out in the woods or suffering sudden heart attacks even though they were young and in otherwise great health). Authorities quickly ruled some of the deaths suicides seemingly without even really investigating the circumstances surrounding the death. Some of the doctors were linked to each other through their research. These dead doctors all seem to have one thing in common: they were studying the effects of GcMAF and/or nagalase in regards to cancer patients or links in children with autism. We’ll get to what exactly those two things are in a moment.

One of the more high profile murders was that of Dr. James Bradstreet, whose body was discovered floating in a North Carolina river, a single gunshot wound to his chest (via Natural News):

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.

As we all know, cancer is big business in this country. We’re talking about a 124 billion dollar industry. A number that big is naturally a matter of “national security”. One of our countries biggest products is cancer, so why anyone believes the system would ever allow a cure is beyond me.

As such, it should come as no surprise information about groundbreaking research on GcMAF’s cancer-fighting ability has not been widely distributed. In fact, we didn’t learn about it at all until doctors started dying for researching it. While those who worked with it claimed it has reversed autism and cured cancer in studies (studies which had to be kept on the low down), consider this on the flip side: if the body is somehow inhibited in any way from producing GcMAF, the person’s immune system is utterly compromised, allowing for all manner of diseases. This compound (or lack thereof) is linked to autism, cancer, diabetes, you name it. Without the body’s ability to produce GcMAF, a person is set up to get sick and eventually die.

An enzyme called nagalase excreted by cancer cells (and which is also a component in the envelope protein of viruses like HIV and influenza) is known to inhibit the body’s production of GcMAF.

Dr. Bradstreet et al. had all discovered in one way or another that nagalase is compromising the immune systems of people with autism and cancer etc. by inhibiting their bodies from producing GcMAF, but…

Here’s the bombshell: many of these dead doctors believed nagalase was being PURPOSEFULLY ADDED to the vaccines.

Why? Population control.

If you haven’t heard about this, you have to listen to this 19 minutes of an interview with Dr. Ted Broer on Hagmann & Hagmann.

The full interview can be found here. The interview didn’t even happen for the first hour because the site kept having mysterious technical difficulties while the show was on and the doctor kept getting disconnected. He begins by letting the audience know he is not suicidal. Via Dr. Broer in this 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 a while. 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 Food and Drug Administration 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 is 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.

…Macrophages in the body are the ones that kill cancer cells. They stop cytokine storms… the GC protein in the body adds vitamin D to it… How many times have I told the listeners you have to take vitamin D every day? That’s super important. Remember GC protein gets vitamin D added to it and the GC protein becomes what’s called GcMAF (Gc protein-derived macrophage activating factor)… This GcMAF protein is human immune system enzyme protein also known as vitamin d binding protein…

This GcMAF is probably the single most effective thing in the immune system to kill cancer cells

…and what’s happening is, the immune system is being compromised by a product called nagalase.

Again, when GcMAF is inhibited, it compromises a person’s entire immune system. Period.

What these doctors found was this… that this nagalase protein enzyme they felt was being introduced into the body either virally or directly through immunizations. This is the enzyme protein that destroys the immune system.

I’m going to repeat this. Apparently since these guys are dead and I can’t talk to them. They have found that the nagalase enzyme protein that was made by cancer cells and viruses which causes immunodeficiency is being added through the immunizations either through viruses or through the immunization itself being given nagalase.

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.

I’m not saying what happened to these guys, I’m just saying they’re not on this planet anymore. (Read more on this story at Natural News here and here.)

Nagalase was, surprise surprise, being found in very high concentrations in children with autism. Nagalase testing is also done for cancer, AIDS, and other chronic infections.

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.

Dr. Broer goes on to talk about how GcMAF given to autistic children has completely erased their symptoms. That it has cured cancer. Alzheimer’s. The list goes on and on.

So, to sum it up, nagalase inhibits GcMAF, a lack of which compromises the immune system, and nagalase is linked to autism, cancer, and all manner of diseases, and the dead doctors had reportedly all figured out in one way or another that  nagalase molecules was purposefully being added to our vaccines as slow kill.

That’s the theory. Think about that for a second. Let it sink in.

And we’re told we’re horrible monsters if we don’t shoot our kids up with massive doses of vaccines because they might get measles.

 

 

The United States has the most aggressive vaccination schedule on the planet, and yet, we have one of the highest rates of infant mortality, autism is skyrocketing year after year, cancer is one in three for women and one in two for men, and pretty much every disease you can think of is on the rise here. While the vaccine link to autism has been widely discussed in alternative circles as the incidences of autism have risen sharply over the past decade, many know there’s a connection but are unsure of just precisely how it works. Is it the heavy metals? The genetically engineered DNA? The barrage of chemicals, including polysorbate which acts as a detergent to help the chemicals in vaccines cross the blood-brain barrier more easily?

Or… is the answer much, much simpler?

Is it the addition of a known immune-system inhibiting enzyme that leaves all of us and our children immune compromised from birth and essentially set up to get sick and die?

Depopulation 101… add poison to vaccines… make it law that all children must be injected to attend school. Slow kill methods. They think they’re being fair w/ their “survival of the fittest” type mentality. Only the best genes survive? These people have no souls. (source)

We could ask a dozen doctors what they think about that theory, but… they’re all dead.

In the meantime, Dr. Broer suggests everyone take Vitamin D3 every day.

Man this world is so beyond screwed up.

And look, here’s a vaccination commercial now!

 

Melissa Dykes (formerly Melton) is a co-founder of TruthstreamMedia.com where this article first appeared (used with permission). She is an experienced researcher, graphic artist and investigative journalist with a passion for liberty and a dedication to truth. Her aim is to expose the New World Order for what it is — a prison for the human soul from which we must break free.

 

Doctors are being killed for killing our children

several alternative doctors have died in Florida

who were interlocked to Dr James Bradstreet and other doctors

who were doing important  research relating to the use of GCMAF on curing autism, cancer, diabeties

see short video

https://youtu.be/XYvLPCze_So

 

To see the full interview

https://www.youtube.com/watch?v=8g0NMH4RXZ4

 

GC Protein, used by macro fages in the body and kill cancer cells

GC protein adds vitamin D to the body

we must take Vitamin D 

GCMAF

Vitamin D

 

Vitamin D in the body is being compromised  by nagalase molecules

Apparently these dead Drs found that the N Enzyme protein is being added through the immunisations 

The nagalase molecules in viral protein causes the cancer

 

Nagalase causes immunodeficiency and prevents the immune system from doing its job

 

Dr Kim Smith MD wrote a book on this

Nagalase attacks proteins in the body

Nagalase  never misses its target

GCMAF

Children had very high Nagalase  after the immunisation

 

CFMAF

treatment of cancer and viral disease

can buy on line

CFMAF is a vital part of the immune system

 

Dr James Bradstreet

treated 1,100 autistic patients with CFMAF 

had 85% positive results and  15% were completely cured from autism.

 

  CFMAF cures breast prostate and kidney cancers

stimulates mico fages

CFMAF cures autism, chronic fatigue, alzheimer disease

 

Vitamin D and Type 2 diabeties

low level of vitamin D levels

to  Type 2 diabeties

when fats cells get too large they die

people with diabeties

macrofages at work cause cytokine storm

type 2 diabeties

killed every one of the Spanish flue in 1819

 

 

One of the conditions just after an immune shot

causes the brain to swell, and the brain is pressing against the skull

causing children to scream for at least a day

GCMAF

 

https://youtu.be/XYvLPCze_So

A cytokine storm, also known as cytokine cascade and hypercytokinemia, is a potentially fatal immune reaction consisting of a positive feedback loop between cytokines and white blood cells, with highly elevated levels of various cytokines.

causing scitzophrenia, alsymers etc

 

Cytokine storm - Wikipedia, the free encyclopedia

https://en.wikipedia.org/wiki/Cytokine_storm

•  

A cytokine storm, also known as cytokine cascade and hypercytokinemia, is a potentially fatal immune reaction consisting of a positive feedback loop betweencytokines and white blood cells, with highly elevated levels of various cytokines.

‎Symptoms - ‎Cause - ‎Role in pandemic deaths - ‎Treatment

The advent of the cytokine storm

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by IA Clark - ‎2007 - ‎Cited by 57 - ‎Related articles

The term 'cytokine storm' is now used in popular culture as an explanation for the distinctly unpleasant feeling we all sense at the onset of flu. The expression ...

Into the Eye of the Cytokine Storm

www.ncbi.nlm.nih.gov › NCBI › Literature › PubMed Central (PMC)

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by JR Tisoncik - ‎2012 - ‎Cited by 170 - ‎Related articles

Summary: The cytokine storm has captured the attention of the public and the scientific community alike, and while the general notion of an excessive or ...

Cytokine Storm and the H5N1 Influenza Pandemic: The Bird ...

www.cytokinestorm.com/

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A cytokine storm is the systemic expression of a healthy and vigorous immune system resulting in the release of more than 150 inflammatory mediators (cytokines, oxygen free radicals, and coagulation factors).

What is a "cytokine storm," and what are the diseases that ...

https://www.quora.com/What-is-a-cytokine-storm-and-what-are-the-disease...

Jul 28, 2014 - Cytokine storms are thought to be at the heart of the 1918 influenza pandemic [5] and the 2003 SARS epidemic [6], which affected ...

What is the Cytokine Storm? (with pictures) - wiseGEEK

www.wisegeek.org/what-is-the-cytokine-storm.htm

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Jan 26, 2016 - A cytokine storm is an over-protective immune response that can actually be fatal. Cytokine storms occur when the body sends too...

Cytokine Storm / Cytokine Storms - Sino Biological Inc.

www.sinobiological.com/Cytokine-Storm-Cytokine-Storms-a-5800.html

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The cytokine storm has captured the attention of the public and the scientific community alike, and while the general notion of an excessive or uncontrolled ...

Cytokine storms - Why they are dangerous and can kill ...

https://sites.google.com/.../cytokin-storms---why-they-are-dangerous-and...

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The most serious complication in relation to serious influenza illness is the virus' ability to spark a cytokine storm after the infection has subsided - especially in ...

'Storm' Caused by Emergent Flu Infections - The Scripps ...

https://www.scripps.edu/news/press/2014/20140227oldstonerosen.html

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Feb 27, 2014 - “This study provides insights into mechanisms that are chemically tractable and can modulate these cytokine storms,” said Hugh Rosen, ...

Cytokine storm | definition of cytokine storm by Medical ...

medical-dictionary.thefreedictionary.com/cytokine+storm

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A potentially fatal hyperrelease of inflammatory mediators in response to stimulation of T cells and macrophages by pathogens and immune insults. Triggers ...

 

http://www.nature.com/icb/journal/v85/n4/full/7100062a.html

 

Immunology and Cell Biology (2007) 85, 271–273; doi:10.1038/sj.icb.7100062

The advent of the cytokine storm

Ian A Clark

Correspondence: , School of Biochemistry and Molecular Biology, Australian National University, Canberra, ACT 0200, Australia. E-mail: ian.clark@anu.edu.au

The term 'cytokine storm' is now used in popular culture as an explanation for the distinctly unpleasant feeling we all sense at the onset of flu. The expression certainly has common currency, with 21 000 Google hits 12 months ago and 55 000 at the time of writing this article. The two-part Special Feature in the January and February issues of Immunology and Cell Biology acknowledges that the sense of this term, with the added complexity of knowing that the mediators involved are also necessary, at lower concentrations, for innate immunity to function, has finally come of age. While the articles on HIV, hepatitis, flaviviruses, tuberculosis, toxoplasmosis, shigellosis, schistosomiasis and visceral leishmaniasis essentially concern local pathological events from these cytokines, those on poxviruses, dengue, influenza and malaria describe variants of the consequences of a systemic response. Salmonella, because of its range of serovars, has a foot in each camp. The interesting omission is sepsis. Research into this condition has never managed to gain a foothold in some countries, despite it being the major cause of death in intensive care units in all first world countries and a part of the cytokine storm literature since 1981.

In 1993 a group in Boston,¹ perhaps mindful of the recent Desert Storm war, coined 'cytokine storm' to describe their observations in graft-versus-host disease (GVHD). As we have reviewed,² the notion that excessive release of pro-inflammatory cytokines causes GVHD pathology already existed. For instance, in 1987, a polyclonal anti-tumour necrosis factor (anti-TNF) antibody was shown to reduce mortality in a mouse model of this condition.³ The term next appeared in 2002 as a description of the disease mechanism in pancreatitis.⁴ As with GVHD, the idea was older than the aptly descriptive term, with a pro- and an anti-inflammatory cytokine being incriminated in this condition in 1992⁵ and 1997,⁶respectively. The role of excessive release of such cytokines in pancreatitis, along with other examples of tissue injury (trauma, burns) causing disease by excessively activating systemic inflammation, is also covered in the review mentioned above.²

The first use of cytokine storm to describe the mechanism of an infectious disease was probably observed a year later, in 2003, in influenza encephalopathy.⁷ Subsequently, it was applied to variola virus⁸ and H5N1 influenza.⁹ Thus, people new to the concept can be forgiven for assuming it began in non-infectious examples of systemic inflammatory disease and was then also seen to apply to diseases caused by infectious agents. In fact it began in infectious disease in 1981, malaria in particular, although it has been argued from the beginning to be also relevant to systemic Gram-negative bacterial infections and its iatrogenic twin, the Jarisch–Herxheimer syndrome.

Although cytokine storm can be a useful lay term, we must expect clinical and pathological dissimilarities in systemic diseases that have this common fundamental origin. Different triggers for cytokines (lipopolysaccharide (LPS), Gram-positive toxins, fungal toxins, glycosylphosphatidylinositol (GPI) or modulation of RIG-1 gene expression) can be expected to generate different ranges, profiles, concentrations and kinetics of cytokine and chemokine generation and release. Different sites (for example, restricted to one or more tissues, or circulating) of release are obvious additional causes for these differences.

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Origins of the concept, in malaria

Like most observations that beget paradigm changes, this one was not being sought when found. As has been reviewed a number of times over the past few decades,^10, 11 our group was trying to understand how pretreatment with the Bacillus Calmette-Guérin (BCG) strain of Mycobacterium tuberculosis controlled a subsequent infection with several strains of haemoprotozoa in mice. No antibody was induced, yet parasites were dying in circulating red cells, not after phagocytosis, as BCG protection might predict. The timely publication of the first paper on tumour necrosis factor (TNF),¹² allowed us, in collaboration with these New York tumour researchers, to propose, in 1981, the dual roles of TNF and other cytokines in immunity and disease pathogenesis in malaria and sepsis.^13,14 Some 40 key background papers that demonstrate the development of the idea of TNF being much more than a tumour killer are shown in Table 1 of a 2003 review.¹¹ While this was years before access to the tools was made possible by rTNF, the key predictions of the model stood the test of time once they became available.^{15, 16, 17, 18} The too rapid appearance and clearance of TNF in acute illness is presumably what prevented neutralizing antibody from being clinically useful, since it prevented illness when given before antibiotic treatment in the Jarisch–Herxheimer syndrome.¹⁹

Nowadays, when a TNF superfamily of at least 19 members signalling through 29 receptors has been described,²⁰ it warrants recalling that in the 1980s this complexity was not countenanced. Moreover, rTNF was then freely available for laboratory studies from large batches, manufactured in anticipation of its use in treating tumour patients, that proved to be too toxic because of influenza/malaria-like side effects.^21, 22 For a while, this gave TNF an artificial prominence in the literature over other similar cytokines, and it was not until 1992 that we were able to acquire recombinant lymphotoxin (courtesy of Bharat Aggarwal) in quantities that allowed studies parallel to those of TNF.²³

Viral diseases

Our group's interest in understanding why malaria and influenza are so clinically similar led us, in 1989, to propose that influenza and other viral diseases (we argued the case for hepatitis B, influenza, dengue and yellow fever), like malaria, have an inflammatory cytokine origin.²⁴ In 1993, the main CDC filovirus group²⁵ was still promoting the idea that increased endothelial cell permeability in filovirus infections was caused directly by viral invasion of these cells and multiplication within them, but, within a few years, they had espoused inflammatory cytokines by demonstrating that the observed increased permeability was instead the consequence of virally-induced TNF from monocytes and macrophages.²⁶ Since then, the literature on the pathogenesis of serious viral infections, including those caused by a hantavirus, Marburg and Ebola viruses, Lassa and Junin viruses, dengue viruses and influenza virus, has become focused almost exclusively on arguments favouring a central role for inflammatory cytokines.

As noted above, the idea also took root for influenza,²⁷ particularly for the more pathogenic strains. For example, good evidence now exists that influenza A virus stimulates the release of TNF from macrophages^28, 29 and that the avian influenza virus, H5N1, which is particularly virulent in humans, generates more TNF in human macrophages than do a range of less virulent strains of human influenza.³⁰ The same is true of the ability of H5N1 to induce inflammatory cytokine responses in primary cultures of human alveolar and bronchial epithelial cells.³¹ In addition, TNF-related apoptosis-inducing ligand (TRAIL) and TNF mRNA are upregulated in human monocyte-derived macrophages infected with H5N1/97 virus,³² and higher levels of inflammatory cytokines and chemokines are associated with a fatal outcome.³³ Moreover, a reconstructed version of the strain of influenza virus responsible for massive human mortality in 1918–1919, but not non-virulent constructs or strains, has recently been reported to induce a strong and prolonged pro-inflammatory cytokine response during the fatal infections it causes in mice³⁴ and macaque monkeys.³⁵

The ICB Special Feature contribution on influenza³⁶ has brought our attention to the possibility of any treatment directed against the systemic inflammation that causes illness in this disease also inhibiting the innate response against the virus. This is a valid possibility, as TNF has been shown to exert a powerful in vitroeffect against influenza virus in human epithelial cells.³⁷ It is curious, however, that with close to a million patients having received long-term TNF-neutralizing drugs for rheumatoid arthritis or Crohn's disease by 2004,³⁸ and a call being made in that year for alertness to the possibility of hepatitis or HIV exacerbation,³⁹ there seems to be no reports of enhancement of viral diseases as yet, including influenza. In contrast, reports of exacerbation of tuberculosis, and various bacteria (Pneumococcus, Listeria, Salmonella and Staphylococcus) are not uncommon.

How Cancer Cells Spread .

news.google.com/newspapers?nid=1798&dat=19730502&id...

... which they have found clues to fighting cancer in the body's immune system the ... Usually these foreign substances would cause a person's system to produce ... And these antibodies do kill cancer, cells in test tubes in the laboratory— but ... a recent inte view in Nogales, Ariz., he American Cancer Societ held its annual ...

REVEALED: Cancer industry profits 'locked in' by nagalase ...

www.naturalnews.com/050582_nagalase_GcMAF_

Ted Broer & Sheila Zilinsky-The Coming Global Meltdown and the Dot That Nobody's Connecting

Published on Dec 19, 2015

Bilderberg, the TPP, Geoengineering, Wireless Radiation, Transhumanism, Nanotech, Artificial Intelligence, CERN and the common thread of all of it.

Doctors are Being Killed for Saving Your Children

So apparently the holistic doctors who were all being killed in Florida had found out via their research that the nagalase enzyme protein is INTENTIONALLY being added to the population via immunizations. Nagalase STOPS vitamin D from binding to the Gc protein. This completely strips a human being’s body of it’s natural ability to kill cancer cells. Nagalase is a protein that’s also created by all cancer cells. This protein is also found in very high concentrations in autistic children. And they’re PUTTING it in our vaccines!! This prevents the body from utilizing the Vitamin D necessary to fight cancer and prevent autism. Nagalese disables the immune system. It’s also known to cause Type 2 Diabetes. So basically…they weren’t  killing these doctors because they had found the cure to cancer or were successfully treating autism… they’re killing them because these Dr’s had been researching and had the evidence that the vaccines they’re injecting our precious children with are CAUSING our current cancer and autism crisis!! And that it’s obviously being done knowingly and on purpose! The doctors they killed in Florida had been collaborating and were getting ready to go public with the information.

Depopulation 101..add poison to vaccines…make it law that all children must be injected to attend school. Slow kill methods. They think they’re being fair w/ their “survival of the fittest” method . Only the best genes survive? These ppl have no souls.

Dr Ted Broer breaks the above info (about the nagalese) in this clip. He explains it much better than I do. The clip is short (from his July 25th Hagmann & Hagmann interview) but it’s a MUST listen. Dr Ted Broer broke it on The Hagmann & Hagmann Report and it took them a whole hour just to get him on air b/c their 3 hour show was brought down and every line they tried to use kept disconnecting..and then their servers were brought down. They asked a bunch of ppl to pray against the attack and then finally got him on a secured line..and so a full hour into the show they were finally back on the air and connected to Dr Broer and the first thing he said was “I am in no way suicidal.” He was super nervous holding onto this info…afraid he’d be taken out Hastings style before he got a chance to say it publicly. So listen to this short clip of him breaking the story. It’s a 19 min clip but the most important info is heard within the first 10 min. It is def some of the most important news I’ve ever heard. And it needs to go viral. PLEASE LISTEN TO THIS SHORT CLIP!!

Source: http://therebel.is/en/?option=com_content&view=article&id=850353:murdered-holistic-doctors-had-discovered-autism-cancer-causing-enzyme-intentionally-being-added-to-all-vaccines&catid=218:guest&Itemid=5582#discuss-850353

MIT Researcher’s New Warning: At Today’s rate, Half of All U.S. Children Will Be Autistic by 2015

Graph of Monsanto’s Roundup Use Vs Children with Autism

 

MIT Researcher’s New Warning: At Today’s Rate, Half of All U.S. Children Will Be Autistic (by 2025)

Stephanie Seneff is a Senior Research Scientist at the MIT Computer Science and Artificial Intelligence Laboratory. She received the B.S. degree in Biophysics in 1968, the M.S. and E.E. degrees in Electrical Engineering in 1980, and the Ph.D degree in Electrical Engineering and Computer Science in 1985, all from MIT. For over three decades, her research interests have always been at the intersection of biology and computation: developing a computational model for the human auditory system, understanding human language so as to develop algorithms and systems for human computer interactions, as well as applying natural language processing (NLP) techniques to gene predictions. She has published over 170 refereed articles on these subjects, and has been invited to give keynote speeches at several international conferences. She has also supervised numerous Master’s and PhD theses at MIT. In 2012, Dr. Seneff was elected Fellow of the International Speech and Communication Association (ISCA).  http://people.csail.mit.edu/seneff/

http://people.csail.mit.edu/seneff/California_glyphosate.pdf

 

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

Monday, July 27, 2015 by: Julie Wilson staff writer
Tags: nagalase, GcMAF, cancer industry profits

(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.

Stay tuned as Natural News continues to uncover more on this investigation.

Sources:

http://www.blogtalkradio.com

http://fortune.com

http://www.naturalnews.com

http://www.naturalnews.com

http://www.washingtonpost.com

http://www.vaccinetruth.org

http://www.naturalnews.com

http://thefreethoughtproject.com

http://www.timsmithmd.com

more: http://www.naturalnews.com/050582_nagalase_GcMAF_cancer_industry_profits.html#ixzz415doQbDX

http://www.naturalnews.com/050582_nagalase_GcMAF_cancer_industry_profits.html

Learn more: http://www.naturalnews.com/050582_nagalase_GcMAF_cancer_industry_profits.html#ixzz415dTAcKB

 

                                                              http://firstamendmentradio.net/

                                            What is the Cytokine Storm?

 Cytokine storm is the body's over-reaction to infection.

The most serious complication in relation to serious influenza illness is the virus' ability to spark a cytokine storm after the infection has subsided 

                                                                                                       http://www.wisegeek.org/what-is-the-cytokine-storm.htm

People often think of external microbes as their worst enemy during an outbreak ofinfluenza or bronchitis, but the body's own immune system is potentially more lethal.
When the body detects foreign microorganisms indicating an infection, it might respond by over-protecting the site of infection. It may race so manyantibodies 
to the infection site that they collect in a cytokine storm. When the infection is in the lungs, for example, this response can potentially block airways and result in suffocation.
Medical researchers have identified the causes and stages of the reaction and are working on treatments to weaken an overactive immune response.

At all times, white blood cells circulate in the bloodstream and are the first to sense if a virus or bacteria has infiltrated the body. Immediately,
other immune cells, including T-cells and macrophages, are sent to attack the infection. During this stage, a person's immunity functions properly,
and immune cells attack the microbes so they do not get too strong a foothold.

For reasons that are not completely understood, too many immune cells can be sent to the infection site.
This happens when a particular type of molecule in the body, known as cytokines, activate the immune cells at the infection site and
cause more immune cells to flood the site of infection. This propagates what is referred to as a cytokine storm,
where far too many immune cells are caught in an endless loop of calling more and more immune cells to fight the infection.
The reaction ends up inflaming the tissue surrounding the infection.

When the infection is in the lungs, this severe inflammation can cause permanent damage. A prolonged cytokine storm
will eventually shut down breathing completely. The airways get clogged, and cells no longer properly absorb oxygen.
This is what makes the reaction so deadly in certain epidemic strains, such as bird flu. Even bronchitis, other varieties of influenza, pneumonia, sepsis, and possibly rheumatoidarthritis are susceptible to triggering a cytokine storm.

Of course, flu vaccines are usually effective at preventing the flu during its peak season, but they are no guarantee,
especially when flu strains mutate after the vaccine has been manufactured. Therefore, researchers are pursuing other methods
of preventing this extreme immune response by bioengineering a drug that could slow the snowball effect of antibodies.
They hope to force the cytokines to recirculate in the bloodstream, rather than pool in the area of the infection.
Experts predict that a major influenza pandemic could kill millions of people worldwide, as it has done in centuries past.

http://topics.wisegeek.org/topics.htm?cytokines-storm#

Cytokines Storm on wiseGEEK:

• A phenomenon involving the function of inflammatory cytokines is sometimes known as a cytokine storm. Essentially, this is a situation where the balance of communication between immune cells and the cytokines present is interrupted.
  
  
• Genes of those sometimes contain codes for enzymes involved in platelet activation and production of nitric oxide. Proinflammatory cytokinesalso include chemokines that can let immune cells called leukocytes get from the blood into infected tissues.

http://topics.wisegeek.org/topics.htm?cytokines

Cytokines

Cytokines on wiseGEEK:

• Genes of those sometimes contain codes for enzymes involved in platelet activation and production of nitric oxide. 
• Proinflammatory cytokinesalso include chemokines that can let immune cells called leukocytes get from the blood into infected tissues.
  
  
• The primary role of cytokines includes regulation and communication. 
• Cytokines are often produced by the body in reaction to conditions of imbalance, including illness and physical trauma, 
• and is an attempt to marshal other parts of the body to help restore proper balance.

http://topics.wisegeek.org/topics.htm?cytokine-assay

Cytokine Assay on wiseGEEK:

• There are several common types of a cytokine assay, many of which are variations on the enzyme-linked immunosorbent assay (ELISA), 
• which works by fixing the receptor for the cytokine is fixed to a surface.
  
  
• Researchers studying mice can use a cytokine assay to see which cytokines are present in their research subjects, and in what concentrations.

Robby the Robot /// IMAGE CREDIT: Photojunkie [Public domain], via Wikimedia Commons

There’s a 50% Chance a Robot Will Take Your Job in the Next 20 Years 

 

Job loss is blamed on many factors. Illegal immigration (though this argument is dubious at best), outsourcing, regulatory overreach, and automation are the most common culprits. Of these, automation — specifically the rise of a robotics-based labor force coupled with artificial intelligence (AI) — poses the greatest threat to the average job. Advances in robotics and AI may soon endanger the employment status of everyone from drivers and personal assistants to sex workers and writers. According to a CNN report, the Bank of England is preparing for automation to shed 80 million American jobs and 15 million British jobs within the next 10 to 20 years. This is approximately 50% of the U.S. and British workforce. Forbes has put the number at 45%.
The workers who will be replaced first are toll booth operators, cashiers, marketers, customer service reps, factory workers, financial middlemen, journalists, lawyers, and phone workers. These jobs will soon be supplanted by automated services made possible by AI, 3D printing, robotics, nanotechnology, and even biotechnology.
Sourcing a study from Oxford University, Yahoo Tech adds even more jobs to the endangered list, including paralegals, loan officers, receptionists, salespeople, security guards, fast food cooks, and even bartenders.
“We are approaching the time when machines will be able to outperform humans at almost any task,” says Moshe Vardi, a computer science professor at Rice University in Texas. “Society needs to confront this question before it is upon us: if machines are capable of doing almost any work humans can do, what will humans do?”
The transformation is already underway, and the World Economic Forum (WEF) believes five million jobs will be gone by 2020, irrevocably terminated by what they call the “Fourth Industrial Revolution.” The jobs most at risk in the immediate present, the WEF says, are “administrative and routine white-collar office functions,” though eventually advances in AI will provide corporations with the option of outsourcing virtually any job to automated services and entities.
What can humans do? The WEF recommends “upskilling.”
At least one analyst is more optimistic on the issue. J.P. Gownder of Forrester, a Boston-based tech research firm, says robots will replace some jobs, but will also create new ones. The new jobs, Gownder believes, will be training the robots.

This article (There’s a 50% Chance a Robot Will Take Your Job in the Next 20 Years) is free and open source. You have permission to republish this article under a Creative Commons license with attribution to Jake Anderson and theAntiMedia.org. Anti-Media Radio airs weeknights at 11pm Eastern/8pm Pacific. -

http://governamerica.com/issues/global-issues/mind-control-propaganda/transhumanism/21735-there-s-a-50-chance-a-robot-will-take-your-job-in-the-next-20-years

Police Shoot Suicidal Dad 11 Times… While He Lay in Bed Crying

Category: Police State

Published on Thursday, 18 February 2016 17:18

Piper McGowin

The Daily Sheeple
February 16, 2016

 

We’ve reported before on how calling the police for help these days in the modern American police state usually ends in less help and more death, pets included.
This time the woman was actually calling for an ambulance and not the cops, but since all first response tech is now integrated, the cops were sent anyway.
The Charleston Gazette-Mail reports:

Donna Spry called her husband’s doctor, crying. Curly Spry was refusing to go to his appointment. He was suicidal, off his medication and had a gun, his wife said.
Call 911, the doctor’s staff instructed her.
Less than an hour later, Curly Spry was dead. He had been shot 11 times by troopers with the West Virginia State Police, according to a lawsuit filed by Donna Spry last month in Kanawha County Circuit Court.
The family is suing for $11 million—their attorney told the Gazette-Mail that the agency’s insurance covers $1 million per incident. Suicidal Curly Spry was delusional and crying and laying in bed. His wife and 17-year-old daughter were reportedly standing by his bedside when state police shot him 11 times.
Eleven.

The Sprys allege the troopers came into their house without permission. They wore full tactical gear and had weapons in hand when they entered, according to the complaint.

Spry’s wife claims she was on the phone with 911 when they killed her husband, and a trooper made her hang up afterwards. Of course, the police said the man pointed a gun at them (while he was laying in bed crying and they were wearing full tactical gear including bullet proof body armor)… so they just had to shoot a weeping suicidal man 11 times while he was lying in bed.

Guess Mr. Spry doesn’t have to worry about being suicidal anymore.

http://governamerica.com/issues/domestic-issues/homeland-security/police-state/21738-police-shoot-suicidal-dad-11-times-while-he-lay-in-bed-crying