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Dead Doctors and the GcMAF Connection

See New Study: Diseases Declined Long Before Related Vaccines Implemented

14 doctors now dead or missing in the past 6 weeks. What is the connection? This information impacts you because the information being covered up is critical for your health and personal safety! Please share this video with everyone you know.

"4 days after GcMAF-primed immunization of mice with heat-killed Ehrlich ascites tumour cells, the ascites tumour was no longer transplantable in these mice."

Vital Links
Do vaccines prevent disease?
What Vaccines Do To The Body




All About GcMAF


GcMAf is something your body makes and you are born with.

In the past months Dr. Bradstreet has become interested in nagalese, which he describes as an enzyme "produced by cancer cells and viruses" This is the connection between an enzyme ONLY MADE BY CANCER CELLS and vaccines.

There is a connection between NAGALASE and AUTISM. AUTISTIC CHILDREN WERE BORN WITHOUT CANCER - previously disease free - therefore the BIG question is:

How does a CANCER AND VIRUS ENZYME get into the blood of all Autistic - formerly healthy - kids?

It's unlikely that children with autism have undiagnosed cancers, and thus suspicion falls on a viral etiology.

Related: http://www.ageofautism.com/2011/10/dr-bradstreet-nagalase-and-the-viral-issue-in-autism.html

We know flouride is in many baby formulas and that it kicks opens the body's protective BLOOD BRAIN BARRIER which protects the brain from heavy metal toxicity and environmental poisoning such as Chemtrail toxins. There have also been reports about flouride showing up in tests done from soil and water samples due to aerosol spraying programs. Note also that many over-the-counter products also contain fluoride as do many pharmaceuticals

How do viral enzymes that attach and cloak viruses and cancer and are actually only made by viruses

What is in vaccines? Tenuated living and dead viruses.

How are autism and cancer related?

Two internationally known doctors may have lost their lives because they knew about the connection between these two diseases.

Nagalase blocks production of GcMAF, thus preventing the immune system from doing its job. The macrophages are still present in the body, but the nagalase prevents them from waking up and becoming active. This means that cancer and viral infections can grow unchecked while macrophages sleep.

If autistic children don’t have cancer or viral infections, then what is the source of their elevated nagalase levels? If nagalase wasn’t made in their bodies by cancer cells or viruses, then how did it get into the bodies of infants and young children?

According to an informant who wishes to remain anonymous for reasons of personal safety, Dr. Bradstreet and other alternative medical researchers came to understand that nagalase is being introduced into the bodies of people who receive vaccinations. Dr. Bradstreet understood that people have different reactions to nagalase. In fact, a small percentage of people do not experience suppression of their immune systems. However, for the majority, there is dangerous immune system suppression, which opens the door to cancer and autism.

The Gc of GcMAF IS A VITAMIN D BINDING FACTOR

Chemtrails ARE BLOCKING OUR SUNSHINE WHICH MAKES VITAMIN D 3 in our skin. Without the MAF BEING ACTIVE, VITAMIN D MAY BE INGESTED BUT NOT TAKEN INTO THE MACROPHAGE CELLS IN ORDER TO ACTIVATE THEM.

So can we actually connect the CHEMICAL SPRAYING OF TOXINS TO BLOT OUT SUN AS ANOTHER WAY TO INSURE WE WILL ALL BE DEFICIENT IN VITAMIN D AND EVEN IF WE ARE NOT,
OUR DOWNED inactivated GcMAF will not BIND IT to activate the macrophases and boot up our own GcMAF protien.

This is why RAW MILK HAS BEEN MADE ILLEGAL AND WHY PASTURIZED MILK IS IRRADIATED. Pasteurisation destroys Vitamin D in milk and VITAMIN D IS WHAT MAKES OUR IMMUNE SYSTEM ACTIVE. Furthermore, the sun has been DEMONIZED despite that fact that it is a primary source of vitamin D.

We are born with ACTIVE IMMUNE SYSTEMS AND GCMAF

From birth, we are assaulted with VACCINES. ALLOPATHIC MEDICINE SAYS WE MUST HAVE THEIR HELP to stay "disease free". If our immune systems were assaulted in this way with vaccines, we would likely live relatively disease free.

Now we have governments attempting to FORCE-VACCINATE the public OR WITHOLD SCHOOL AND EMPLOYMENT and likely government benefits or professional licences to those who reject vaccines. It is nothing short of medical-genocide being forced on the public while anything natural and FREE IS BEING TAKEN OVER, CONTROLLED, and outlawed.

Part of ALL VIRUS ENVELOPES

VACCINES CONTAIN ATTENUATED AND RECOMBINANT VIRUSES. So logic and common sense cannot deny it is in vaccines. Further, it is THE ONLY WAY NAGALASE CAN ENTER HUMAN BLOODSTREAMS unless bitten by virus containing vector such as mosquitoes. But in this case, your own GcMAF and skin-produced vitamin D macrophage-activated cells would erradicate the virus.

They vaccinate the public from cradle to grave for the purpose of maintaining our dependence on the medical and pharmaceutical industries. Agencies like FDA and EPA shut down all cures that they cannot profit from.

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Structurally well-defined macrophage activating factor derived from vitamin D3-binding protein has a potent adjuvant activity for immunization.
Yamamoto N1, Naraparaju VR.

Author information

1Laboratory of Cancer Immunology and Molecular Biology, Albert Einstein Cancer Center, Philadelphia, Pennsylvania 19141, USA.

Abstract

Freund's adjuvant produced severe inflammation that augments development of antibodies. Thus, mixed administration of antigens with adjuvant was not required as long as inflammation was induced in the hosts. Since macrophage activation for phagocytosis and antigen processing is the first step of antibody development, inflammation-primed macrophage activation plays a major role in immune development. Therefore, macrophage activating factor should act as an adjuvant for immunization. The inflammation-primed macrophage activation process is the major macrophage activating cascade that requires participation of serum vitamin D3-binding protein (DBP; human DBP is known as Gc protein) and glycosidases of B and T lymphocytes. Stepwise incubation of Gc protein with immobilized beta-galactosidase and sialidase efficiently generated the most potent macrophage activating factor (designated GcMAF) we have ever encountered. Administration of GcMAF (20 or 100 pg/mouse) resulted in stimulation of the progenitor cells for extensive mitogenesis and activation of macrophages. Administration of GcMAF (100 pg/mouse) along with immunization of mice with sheep red blood cells (SRBC) produced a large number of anti-SRBC antibody secreting splenic cells in 2-4 days. Thus, GcMAF has a potent adjuvant activity for immunization. Although malignant tumours are poorly immunogenic, 4 days after GcMAF-primed immunization of mice with heat-killed Ehrlich ascites tumour cells, the ascites tumour was no longer transplantable in these mice.

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No vaccine adjuvant is necessary (an adjuvant is part of vaccine containing toxic heavy metals to irritate and inflame an area so cells respond), but GcMAF only requires inflammation to work, so GCMAF is body's own natural vaccine against all inflammation which is disease precursor.

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