Nagalase: The Cause of Autism

Revolutionary suppressed treatment, GcMAF, has the potential to reverse cancer, autism, HIV, liver/kidney disease and diabetes as well as promote proper immunity function.

I have written previous articles observing heavy metals’ and more specifically mercury’s role in the onset of autism spectrum disorders, but another huge factor is at play too; that factor is nagalase which works with heavy metals to cause lasting damages. Nagalase is a dangerous protein generated by viruses, bacteria and cancers; our bodies should be dealing with this autonomously through macrophages, which play an important anti-inflammatory role, but vaccines are becoming the roadblocks to the success of this natural defence mechanism, read on to find out why:

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.

Gc-Protein is a “Macrophage-Activating Factor”, abbreviated as “MAF”

Macrophages, or ‘big-eaters’ from their Greek derived name, are large white blood cells from monocytes, and are crucial to an overall robust immunity. Macrophages release cytokines which deal with infection, immune responses, inflammation, trauma, sepsis, cancer via tumour necrosis factor, and reproduction; mass inflammation being a hallmark of autism. They are also constantly eliminating pathogens and toxins around the body.

Nagalase inactivates these crucial macrophages (you can watch a video of this here).

Autism is a relatively new condition, as is cancer – and there is a cause of this emergence; vaccine ingredients, including the nagalase protein introduced on a widespread level over the past few decades, blocks the immune system from adequately functioning. The result of this is massive, entire-body inflammation, and because of this, a body that ‘attacks’ itself in perpetual defense-mode hysteria, a factor common in autoimmune diseases.

Nagalase has immune-suppression properties which makes sense why those with cancer or children with ASD have elevated levels.

In the opinion of First Immune Biotech, Autism tends to be caused by the MMR and other vaccines putting viruses and mercury into children. A shortage of lipids may contribute. Another Italian court has awarded €178,000 against the government to a family who’s child contracted autism from MMR.

These viruses sabotage the immune system by sending out nagalase to prevent the production of the child’s GcMAF, and therefore become chronic.

Autism is usually a viral disease to a greater or lesser extent, with viruses in the brain and the stomach. In 15% of children viruses are negligible, and GcMAF probably will not help. In 85% viruses are involved, and they will respond to GcMAF. In 15% of children autism is mainly a viral disease, and these children make full recoveries.

GcMAF has three excellent effects in the brain and rebuilds the immune system, which then attacks the viruses that cause autism. Improvements in the child are often seen as early as five weeks – about the same time it often takes to permanently eradicate the herpes virus.   We recommend a child starts at 0.03ml, with a second 0.03 dose in three days, to build up to a twice weekly 0.1ml dose as soon as possible. Make sure he eats plenty of lipids.

Children with autism often have very high levels of vitamin D3, occasionally toxic levels (and low levels of D2) which may be produced by gut bacteria. We do not recommend any change to vitamin D3 (which may result in severe hyperactivity) or any change to anything else, until you are four weeks in with the GcMAF. Even then, not unless the child has had a vitamin D level test. So change nothing else at the time you start GcMAF, or preferably Goleic.

“A universal cancer cure (like GcMAF) 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.” — Mike Adams, Natural News

It is no surprise then, that knowing the body expresses its inner-self through its outer-self, that autism sufferers often hit themselves in a blatant expression of the inner turmoil their body is encountering, due to inflammation – have you ever heard the term ‘pulling my hair out’ — this is an external manifestation of our internal chemistry.

Activated macrophages via GcMAF are the solution to our greatest illnesses.
Nagalase snatches all three sugars, thus inactivating GcMAF. A worthless “deglycosylated” DBP molecule.

Nagalase is remarkably efficient

Because it is an enzyme—a catalyst—Nagalase performs this malicious ritual over and over and over again, and each time it comes away unscathed and unchanged. One Nagalase molecule can thus destroy a huge quantity of GcMAF precursor molecules.

To appreciate how precisely Nagalase (Alpha-N-acetylglucosaminidase) targets GcMAF production, imagine a Stinger heat-seeking ground-to-air missile tracking a fighter jet. Evasive maneuvers—even by the best pilots—won’t outsmart the Stinger, which rapidly adjusts its course to track the plane down and blow it up. Nagalase works the same way: it tracks down and then pulverizes the (DBP) precursors of GcMAF molecules.

Nagalase has no natural enemies. No bodily process, no drug, no treatment could outsmart this diabolical killer. Sure, high-powered drugs and radiation will take out many of the cancer cells and in some cases produce a cure, but until Dr. Nobuto Yamamoto came along and outed Nagalase, we had no idea as to the actual cause of the immune shutdown that let cancers and viruses go wild.


Dr. Jeffrey Bradstreet claimed to have tested approximately 400 children with autism for the viral marker, nagalese, and found that nearly 80% have significantly elevated levels.

The normal levels of nagalese at any one time in the human body should be at baseline levels of < 0.95. A healthy college student with a nagalase level of 0.4 is not uncommon.

Many autism and cancer patients have levels much, much higher than this.

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.

In 15% GcMAF makes no difference. 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.

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.

Nagalase inactivates GcMAF?

The enzyme “Nagalase” completely eliminates the sugar side chain of the Gc protein: the thus-modified Gc protein can no longer be converted to Gc MAF, its immune-stimulatory effect is no longer available. In other words, the effect of Nagalase on Gc Protein prevents the formation Gc -MAF. Insofar, tumor-derived Nagalase may have immune-suppressible properties.

  • Nagalase is an endogenous enzyme in sugar metabolism
  • Tumor cells can produce Nagalase; sources can be a retrovirus, herpes viruses, influenza, intestinal bacteria, HERVs.
  • Altered intestinal flora and changes in gut permeability may be a major factor in this entire clinical picture
  • Gc MAF is a macrophage-activating factor , which is produced from Gc-Protein
  • Nagalase produced by tumors can prevet the formation of Gc-MAF from Gc-Protein.
  • Artificially produced Gc-MAF is used as an immune-stimulatory compound
  • The amount of detectable serum Nagalase is measured to check whether a Gc-MAF therapy should be considered (therapy indication) and to monitor the effect of Gc-MAF therapy ( “therapy monitoring”)
  • Additional laboratory parameters are thought to be of importance for Gc -MAF therapy: Vitamin D and calcium levels in blood, the genetic variants of the vitamin D receptor, and the serum levels of soluble uPA receptor.

The Real Reason Holistic Doctors Are Being Murdered and Vanishing is as follows:

  • The introduction of the Nagalase protein in the vaccine provably causes autism and other chronic negative health conditions. When Nagalase is introduced in the human body via vaccines, it blocks the natural occurrence of GcMAF in the human body, this sends the biological balance of the human body out of sync — the result is Autism.
  • 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.
  • GcMAF treatment can reverse autism conditions by up to 85%, according to GcMAF.se.
  • GcMAF can also reverse, deplete and eliminate cancers.
  • Nagalase is present in higher amounts in the bodies of autism sufferers than non-sufferers.
  • Dr. Bradstreet was killed for revealing and disseminating this truth.

Why the Medicines and Healthcare Regulatory Agency (MHRA) is corrupt:

Taken from GcMAF.se please refer to this website to purchase GcMAF for self-treatment.

  • The MHRA banned GcMAF, the body’s way of curing cancer with no side effects.
  • 10 public bodies state the MHRA is corrupt.
  • 13,000 have petitioned to disband the MHRA.
  • It licenses drugs that kill, and provably cause illness, incl. Chemotherapy, vaccinations etc.
  • The MHRA helped conceal GcMAF for 26 years.
  • They destroyed Britain’s GcMAF Co., Immuno Biotech Ltd.
  • Got Immuno Biotech’s scientists and doctors fired.
  • Got its CEO, David Noakes, arrested.

The following video adds more detail to the summarising contents of this article:

If you are considering GcMAF treatment, I would strongly suggest reading this free book that details the process in-detail necessary for successful injected or cream-applied GcMAF.

You can access that by clicking here.

Nagalase, a ‘stealth’ bomber (from Natural News):

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. Perfect for someone with an agenda that wants specific results.

Other relevant articles include:

Nagalese ‘locks-in’ $100 billion cancer profiteering from big-pharmaceutical industry. Explaining the widespread push for vaccines.

Strange disappearances/deaths of holistic health doctors, including key GcMAF progenitor, Jeffrey Bradstreet.

Immunotherapy in chronic diseases

Thyer, Lynda, et al. “THERAPEUTIC EFFECTS OF HIGHLY PURIFIED DE-GLYCOSYLATED GCMAF IN THE IMMUNOTHERAPY OF PATIENTS WITH CHRONIC DISEASES.” American Journal of Immunology 9.3 (2013): 78.

Immunotherapy  in Autism

Hoxhaj, Geranda. “The Combination of the Psycho-Pedagogical Treatment with the Neuro Biochemical Intervention in Children with Autism Spectrum Disorders.” Academic Journal of Interdisciplinary Studies 2.9 (2013): 526.

Immunotherapy in HIV-infected cells

Yamamoto, N., Ushijima, N. and Koga, Y. (2009), Immunotherapy of HIV-infected patients with Gc protein-derived macrophage activating factor (GcMAF). J. Med. Virol., 81: 16–26. doi: 10.1002/jmv.21376.

Effects of GcMAF in patients with cancer, autism, chronic fatigue syndrome, Lyme disease, multiple sclerosis, amyotrophic lateral sclerosis. 

Therapeutic effects of highly purified de-glycosylated GcMAF in the immunotherapy of patients with chronic diseases.
Lynda Thyer, Emma Ward, Rodney Smith, Jacopo J.V. Branca, Gabriele Morucci, Massimo Gulisano, David Noakes and Stefania Pacini. DOI : 10.3844/ajisp.2013.78.84. American Journal of Immunology. Volume 9, Issue 3. Pages 78-84.

Therapeutic effects of GcMAF in autism About 85% of subjects show improvement following GcMAF treatment.

Initial Observations of elevated Alpha-n-Acetylgalactosaminidase Activity Associated with Autism and Observed Reductions from GC Protein—Macrophage Activating Factor Injections. James Jeffrey Bradstreet, emar Vogelaar and Lynda Thyer. Autism Insights 2012:4 31–38. doi: 10.4137/AUI.S10485.

Effects of GcMAF on human neurons explain its therapeutic effects in autism, chronic fatigue syndrome, multiple sclerosis and amyotrophic lateral sclerosis.

Vitamin D binding protein-derived macrophage activating factor stimulates proliferation and signalling in a human neuronal cell line.
Morucci G, Fiore MG, Magherini S, Branca JJV, Gulisano M, Thyer L, Ruggiero M and Pacini S. Italian Journal of Anatomy and Embryology (2013) 118 (Suppl. 2): S143 (P28).

GcMAF has a neuro-protective effect against heavy metal-induced neuronal damage. Implications for autism and chronic fatigue syndrome treatment.

Treatment and Prevention of Cadmium-induced alterations on human neurons. Morucci G, Branca JJV, Ruggiero M, Gulisano M and Pacini S. (P29). Italian Journal of Anatomy and Embryology (2013) 118 (Suppl. 2): S144.

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