Category Archives: RESEARCH, STUDIES, DOCUMENTATION

GcMAF – Curing stage 4 cancer

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Cancer lives exclusively on sugar. If you are fighting cancer you must also not each carbohydrates.
With the diet and protocol if you haven’t had too much chemotherapy you can cure terminal Stage four cancer within a year.

The answer may lie in an understanding of nagalese, a protein made by cancer cells and viruses. Nagalese is a primary cause of immunodeficiency given its ability to block the body’s production of GcMAF, otherwise known as “Vitamin D binding microphage activating factor,” a naturally-produced immune regulating compound that aids in fighting what are traditionally considered terminal diseases. Some researchers suggest that nagalese is one of many toxic components found in the immunizations commonly administered to children, including the Measles-Mumps-Rubella vaccine.

Some independently-minded medical practitioners are beginning to acknowledge not only the nagalese-vaccination link, but also that GcMAF possesses great potential for the treatment of cancer and a variety of other illnesses, including autism, inflammation, and viral and bacterial disease.

The most prominent of the seven doctors who’ve been murdered or died under suspicious circumstances is James Jeffrey Bradstreet. As the contents of his blog drbradstreet.org suggest, Dr. Bradstreet has conducted extensive research into the causes of autism. His body was found on June 19 floating in a North Carolina river with a gunshot wound to his chest. Perhaps uncoincidentally, Bradstreet was a strong advocate of GcMAF and had treated over 2,000 autistic children with the substance; 85% exhibited marked improvement under his care.

Mike Adams article

NEW Study: Vaccines, Adjuvants (ie. Squalene, aluminum) cause adverse reactions

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ADJUVANTS and DISEASE  (READ STUDY)

EXCERPTS

Adjuvants are compounds incorporated into vaccines to enhance immunogenicity and the development of these molecules has become an expanding field of research in the last decades. Adding an adjuvant to a vaccine antigen leads to several advantages, including dose sparing and the induction of a more rapid, broader and strong immune response. Several of thesemolecules have been approved, including aluminiumsalts, oil-in-water emulsions(MF59, AS03 and AF03), virosomes and AS04.

Adjuvants have recently been implicated in the new syndrome named “ASIA—Autoimmune/inflammatory Syndrome Induced by Adjuvants”, which describes an umbrella of clinical conditions including postvaccination adverse reactions.

Recent studies implicate aweb ofmechanisms in the development of vaccine adjuvant induced autoimmune diseases, in particular, in those associated with aluminium-based compounds.The idea that the adjuvant component of vaccines could enhance or trigger autoimmunity or autoimmne diseases represents an intriguing observation that may explain a number of adverse reactions observed after vaccination.

271 New Vaccines in Big Pharma’s Pipeline

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BLACK baby NO TEXT

Duty to Warn

Roll Up Your Sleeves Folks, There are 271 New Vaccines in Big Pharma’s Pipeline. Into Whose Bodies Will They be Injected?

By Gary G. Kohls, MD  Vacine Developmental Pipeline as of 2010

In the article is a list of 146 new vaccines that were in the pipeline as of 2010. The list, PhRMA proudly tells us, is now up to 271 new vaccines as of 2013. For a full listing of these vaccine trials, go to: http://phrma.org/sites/default/files/pdf/infectiousdiseases2010%20%281%29.pdf

Editor-in-Chief of LANCET: (6/19/15) “Half of science literature may be untrue”

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Dr. Richard Horton, Editor-in-chief of the Lancet recently published a statement declaring that a shocking amount of published research is unreliable at best, if not completely false, as in, fraudulent.

Richard Horton_The Lancet_USA_NEO_JUn 2015Horton declared, “Much of the scientific literature, perhaps half, may simply be untrue. Afflicted by studies with small sample sizes, tiny effects, invalid exploratory analyses, and flagrant conflicts of interest, together with an obsession for pursuing fashionable trends of dubious importance, science has taken a turn towards darkness.”  READ MORE…

LANCET JOURNAL: Preparation for Global Polio vaccine

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thelancet

Findings

Of the 41 792 adverse event reports submitted, 39 568 (95%) were for children younger than 7 years. 38 381 of the reports for children in this age group (97%) were for simultaneous vaccination with IPV and other vaccines (most commonly pneumococcal and acellular pertussis vaccines), whereas standalone IPV vaccines accounted for 0·5% of all reports.

It must be noted that these authors, Pedro Moro and Dr. Shimabakuru work for the CDC.

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Pedro Moro, MD is the author that covered up and truncated his data on the 2009/10 H1N1 Pandemic vaccine for pregnant women failing to extend his range of study to the 2009/10 year, stopping the range at the 2008/9 season giving the impression that the flu safe was safe for pregnant women.  His title for the H1N1 pandemic study indicated it covered 2009 in the title leading OB/Gyns to believe it covered the 2009 pandemic which it did not.  Because he stopped short of reporting on the 2009/10 (the actual year of the faux pandemic), he led the nation’s ob/gyn’s to believe the flu shot was safe for pregnant women.

Tom Shimabakuru, MD presented his finding (CDC) to a public group in Atlanta, Georgia in 2012.  He presented the VAERS data for the 2009/10 H1N1 PANDEMIC season.  He did not present the data on pregnant women until questioned by a member of the public.  He then pulled out a separate slide that indicated that there was indeed a 4,250% increase in miscarraiges and stillbirths associated with the flu shots given to pregnant women.  One wonders the pregnancy data of 4,250% increase in spontaneous abortions was hidden from the public while Guillian Barre and other adverse reactions that amounted to a 3% increase in incidents  were presented.

See documentation of the cover up by Dr. Pedro Moro

 

Vaccines deliver 4,925 mcg of aluminum by 18 months, safe limit is 25 mcg

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baby-crying-1

READ What a father wrote to his pediatrician

EXCERPT

So doing some math — the following are examples of weight with their corresponding maximum levels of aluminum, per the FDA:

8 pound, healthy baby: 18.16 mcg of aluminum

15 pound, healthy baby: 34.05 mcg of aluminum

30 pound, healthy toddler: 68.1 mcg of aluminum

50 pound, healthy child:113 mcg of aluminum

150 pound adult: 340.5 mcg of aluminum

350 pound adult: 794.5 mcg of aluminum

So how much aluminum is in the vaccines that are routinely given to children?

Hib (PedVaxHib brand only) – 225 mcg per shot

Hepatitis B – 250 mcg DTaP – depending on the manufacturer, ranges from 170 to 625 mcg

Pneumococcus – 125 mcg

Hepatitis A – 250 mcg

HPV – 225 mcg – Pentacel (DTaP-HIB and Polio combo vaccine)

Pediarix-330 mcg – (DTaP, Hep B and Polio combo vaccine)

850 mcg The HEP-B shot alone is almost 14 TIMES THE AMOUNT OF ALUMINUM THAT IS FDA-APPROVED.

Vaccines deliver 4,925 mcg of aluminum by 18 months, safe limit is 25 mcg  Read more…

Chicken Pox and Shingles Conundrum: New Study

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Shingles-2

Introduction

The varicella-zoster virus (VZV) causes two distinct diseases:varicella (i.e. “chickenpox”) and herpes zoster (i.e. “shingles”) [1].Chickenpox, which primarily occurs during childhood, causes anitchy rash for about a week. Complications from chickenpox are relatively infrequent and include pneumonia, bacterial surinfection and encephalitis. Shingles predominantly occurs at older age. It isthe result of a reactivation of VZV, which after chickenpox remains latently present in neural ganglia. This reemergence of the viruscan be assumed to be a consequence of waning cellular immunity.Shingles is characterized by a painful rash on the body and causes on average a more severe and longer-lasting loss of quality of lifethan chickenpox.

 Conclusion

Evidence increasingly suggests that chickenpox vaccination of children risks redistributing health risks toward older generations.  Varicella-ShinglesStudy

Dr. Gary Goldman:  The reason why we are getting SHINGLES

The only reason that “children who get the chickenpox vaccine APPEAR to have a much lower risk of shingles” is that the live vaccine has provided these children with a recent boost to their immunity. However, the vaccine-strain of varicella zoster virus (VZV)–also known as the Oka strain–is genetically different from the wild-type U.S. strain. When a vaccinated child is exposed to an adult with shingles or a child with wild-type varicella, if the strains are sufficiently heterologous, the vaccinated child will break out in chickenpox. It is also possible for the weakened vaccine-strain to revert to a more virulent strain that manifests wild-type pathology. This means when children are exposed to the wild-type strain, even though they may not have a breakthrough infection with chickenpox, they now harbor two heterologous (genetically different) strains of VZV–both of which are at a later time subject to reactivation as shingles. Thus, as they age, they will be even more likely to reactivate with shingles (unless periodically administered booster vaccine doses for life in order to maintain the immunity)–especially if they do not receive exogenous (outside) boosts to their cell-mediated immunity which, in the pre-vaccine era, came from expostures to other children infected with wild-type varicella which provided the adult with a subclinical boost that helped to suppress or postpone reactivattion of shingles.

I would also like to clear up the point that shingles has always been increasing–even prior to the licensing of the varicella vaccine. This statement is true; however, the increases were on the order of 2 to 4% per year (which were likely due to an aging population, or greater access to healthcare). Once a community had widespread distribution of varicella vaccine, increases in herpes zoster were on the order of 20% per year. For example, this source [Yih WK, Brooks DR, Lett SM, et al. The incidence of varicella and herpes zoster in Massachusetts as measured by the Behavioral Risk Factor Surveillance System (BRFSS) during a period of increasing varicella vaccine coverage, 1998-2003. BMC Public Health 2005; 5:68.
32. Schmid DS, Jumaan AO. Impact of varicella vaccine on varicella-zoster virus dynamics. Clin Microbiol Rev 2010; 23(1):202–217] found a 90% increase in shingles over 5 years (1999-2003).