Wednesday, 22 May 2019

How To Cure Cancer

Treating cancer is big business in America — in fact, it's a $200 billion a year business. Yet 98% of conventional cancer treatments not only fail miserably, but are also almost guaranteed to make cancer patients sicker.


Pharmaceutical lobbyists have changed the laws in most western countries so that only their product, the poison of chemotherapy, is allowed to be prescribed by doctors.


The entire public is brainwashed to believe there is no cure for cancer, when there are dozens.

They control organisations.

The FDA in the USA has chemotherapy corporation directors on its board. They want $900 million spent over ten years before they will authorize a new drug. That way they ensure no inexpensive, effective treatment ever makes it.

In the 1930’s they closed down nurse Rene Caisse, who had been curing people with Essiac.

The FDA will license a chemo drug provided it is below LD50. That means in its lethal dose, it kills 50% of lab animals.

The FDA standard for drug safety is known as LD 50, LD stands for lethal dose, and the 50 is the percentage threshold of lab animals poisoned to death by the drug tested. As long as the percentage killed is under 50%, FDA will approve it!

In the UK they fund the MHRA, which licenses drugs. Their men sit on the boards of licensing authorities so the drug companies license their own drugs. That’s why they kill so many – around 2 million people a year including chemotherapy.

Cancer Research UK is still fraudulently raising money for cancer research when more than enough cures have already been found. It rubbishes these, to promote chemotherapy.

This all means that the British people (and everyone else for that matter) are denied all the brilliant scientific discoveries in cancer of the last 40 years, including GcMAF, which eradicates even stage 4 cancer without side effects.

Here are the proven naturally occurring methods of reducing and curing cancer symptoms, concealed from you by the cancer industry:

- The Paleo diet. Cancer feeds off sugar only. Carbohydrates become sugar in the body. If you avoid sugar and carbs, eat meat fish and veg, you’ll often stop stage 3 cancer in its tracks, and usually cure stage 2 cancer.

- Exercise, oxygen, vitamin D in at least 10,000iu a day. Cancer cells are killed by oxygen.

- GcMAF – a human protein, more expensive. But 300 scientists behind it. Superb for stage 4, and for terminal pancreatic cancers.

- Bicarbonate of soda mixed 1:1 with molasses, which act as a trojan horse to get the bicarb into cancer cells. Keep your body alkaline.

- Large dose (10grams plus) Vitamin C infusions (IV) – published by the Riordan Clinic. Or liposomal vitamin C.

- Bitter almonds. Now banned by the pharma/US government mafia as too effective. But also in Apricot seeds and apple pips – vitamin B17 or laetrile.

- Essaic – a selection of herbs, including sheep sorrel, which animals eat to cure their cancer. Used with huge success by Rene Caisse of Toronto. Her hospital was closed by the chemo industry as too serious a competitor. Essaic is available on the internet.

- Curcumin – but it has to be taken IV, and it can be bought in the proper form. Liposomal is also available.

- DCA dichloracetate – a research paper by the University of Alberta, in Edmonton. If you overdose you get neuropathy temporarily. Simply reduce the dose.

- Pureed asparagus and Broccoli spears. Avocado. Red peaches cause apoptosis of cancer cells. Weak, but works for perhaps 10% of people.

- Hyperthermia – tumours cannot stand temperatures above 40 degrees C.

- Reservatrol in very small doses. Larger doses inhibit CYP1BI. Better: Salvesterols: phytonutrients activated by cancer’s CYP1B1

- The right trace metals for the cancer: Dr Thomas Tallberg MD here.



Supporting quotations & evidence:


Most telling, according to Ralph Moss in his book "Questioning Chemotherapy", is that in a good number of surveys, chemotherapists have responded that they would neither recommend chemotherapy for their families nor would they use it themselves.

Dr Dan Harper reported about an unpublished cohort study in which it was revealed that only 9% of oncologists took chemotherapy for their own cancers.

Let’s hear from a couple of physicians and doctors who have not yet succumbed to the heavy hand of the cancer industry:
…as a chemist trained to interpret data, it is incomprehensible to me that physicians can ignore the clear evidence that chemotherapy does much, much more harm than good.

– Alan C Nixon, PhD, former president of the American Chemical Society.

Walter Last, writing in The Ecologist, reported recently on Professor at the University of California, Dr Hardin Jones' statement:
“After analysing cancer survival statistics for several decades, Dr Hardin Jones, Professor at the University of California, concluded “…patients are as well, or better off untreated.”

Dr Hardin Jones’ disturbing assessment has never been refuted.

Professor Charles Mathe declared:
“If I contracted cancer, I would never go to a standard cancer treatment centre. Cancer victims who live far from such centres have a chance.”
“Many medical oncologists recommend chemotherapy for virtually any tumor, with a hopefulness undiscouraged by almost invariable failure,”

– Albert Braverman MD 1991 Lancet 1991 337 p901 “Medical Oncology in the 90s.
“Most cancer patients in this country die of chemotherapy. Chemotherapy does not eliminate breast, colon, or lung cancers. This fact has been documented for over a decade, yet doctors still use chemotherapy for these tumors,”

– Allen Levin, MD UCSF The Healing of Cancer.

Additionally, Irwin Bross, a biostatistician for the National Cancer Institute, discovered that many cancers that are benign (though thought to be malignant) and will not metastasize until they are hit with chemotherapy. In other words, he’s found that many people who’ve been diagnosed with metastatic cancer did not have metastatic cancer until they got their chemotherapy.

Patrick Swayze was diagnosed with stage 4 cancer in March 2008. Although there are successful treatments for pancreatic cancer, like GcMAF,  they were concealed from him, the usual practice for oncologists. They gave him chemotherapy and he died in September 2009.




Recommended book: We Lost the War on Cancer – Review of Alternative Cancer Therapies:

At the beginning of the last century, one person in twenty would get cancer. In the 1940s it was one out of every sixteen people. In the 1970s it was one person out of ten. Today one person out of three gets cancer in the course of their life. This is projected to be 1 in 2, this is a humanitarian health crisis.

The cancer industry is possibly the most prosperous business in the United States. In 2014, there will be an estimated 1,665,540 new cancer cases diagnosed and 585,720 cancer deaths in the US. $6 billion of tax-payer funds are cycled through various federal agencies for cancer research, such as the National Cancer Institute (NCI). The NCI states that the medical costs of cancer care are $125 billion, with a projected 39 percent increase to $173 billion by 2020.

The simple fact is that the cancer industry employs too many people and produces too much income to allow a cure to be found. All of the current research on cancer drugs is based on the premise that the cancer market will grow, not shrink.

John Thomas explains to us why the current cancer industry prospers while treating cancer, but cannot afford to cure it in Part I. In Part II, he surveys the various alternative cancer therapies that have been proven effective, but that are not approved by the FDA.

Cancer and Autism: Mysterious Deaths of Alternative Health Doctors Who Have Real Cures Not Approved by the FDA

By John P. Thomas of Health Impact News.

This article was originally published on July 31, 2015.

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.

Dr. Jeffrey Bradstreet, MD, an alternative autism specialist, and Dr. Nicholas Gonzalez, MD, an alternative cancer specialist, saw the truth and were willing to step outside of the standard allopathic medical model for treating cancer and autism. They were pioneers in their respective fields and both recently died or perhaps were killed because of their successful treatments of sick, suffering and dying patients.

The Death of Dr. Bradstreet

On June 19, 2015, Dr. Bradstreet reportedly shot himself in the chest after his offices were raided by U.S. FDA agents and State of Georgia law enforcement agents. Three days before his death, agents exercised a search warrant to gather information about the use of GcMAF with autistic patients in his clinic. [1]

Human GcMAF holds great promise in the treatment of various illnesses including cancer, autism, chronic fatigue and possibly Parkinson’s. Since 1990, 59 research papers have been published on GcMAF, 20 of these pertaining to the treatment of cancer. [2] 46 of these papers can be accessed through the GcMAF website. [3]

[caption id="attachment_17652" align="aligncenter" width="544"]bradstreet Dr. Jeffrey Bradstreet talking at an AutismOne conference.[/caption]

They were to collect all records, in whatever form, associated with the use of GcMAF. This included patient records.When agents from the USFDA and local state of Georgia law enforcement raided Dr. Bradstreet’s clinic, they had a very specific agenda – they were after everything they could find pertaining to GcMAF. The search warrant stated in part that agents were to gather all Globulin component Macrophage Activating Factor (GcMAF), GCGlobulin, and/or any other products or component substances thereof that constitute misbranded drugs under the Federal Food, Drug, and Cosmetic Act.

GcMAF is a Substance Produced in the Human Body

GcMAF is not a drug, but a natural substance produced in the human body. GcMAF was being produced in Europe and Dr. Bradstreet was using it with his patients. He was conducting clinical experiments the results of which were published in scientific medical journals. [4]

Scientific medical research is also being done on GcMAF for the treatment of terminal cancer. The results are very promising. [5]

Death of Dr. Gonzalez

On July 21, 2015 Dr. Nicholas Gonzalez died. The cause of death was indicated as a heart attack. At the time of this writing, results from an autopsy have yet to be published. He was reported to be in good health. [6, 7]

[caption id="attachment_17653" align="aligncenter" width="560"]Dr-Nicholas-Gonzalez-Smile Dr. Nicholas Gonzalez.[/caption]

Would a healthy man who understood how diet could be used to prevent, reverse and cure disease be someone who was likely to have a heart attack? Was his heart attack just a natural occurrence, or could it have been caused by an external intervention?

In 1975, testimony before the U.S. Congress indicated that a weapon had been developed to shoot a projectile into a victim without the victim’s knowledge, which would introduce a nearly undetectable substance into the body that would cause a heart attack. The victim would be killed without the telltale evidence of normal bloody assignation. [8] How much more sophisticated weaponry has been developed in the last 40 years since that testimony? Are there new ways to permanently silence doctors who stand alone on the outside of conventional medicine and who will not be quiet about the truth they see?

Are the causes of death for these two very well-known alternative medicine doctors coincidental? Are we being told the truth? Is there a connection between their research and their deaths? Was there research about to cut a large hole in the cancer treatment business and the vaccine business? Let’s take a closer look at GcMAF.

The Power of GcMAF to Cure Modern Diseases

What if there was a simple treatment that could reverse all forms of cancer without radiation, chemotherapy, or surgery? What if it was an unpatentable natural substance produced by the human body and could be given to boost the human immune system to such a degree that it could eradicate cancer from the body without side effects? What if that same substance could be given to autistic children and 85% of them would experience improvement in their autism and many would be completely cured? Wouldn’t that be wonderful!

Most people would think so, but there are many major corporations who would see such a substance as a major threat to their financial prosperity. It would be a major threat to the cancer treatment industry, the cancer drug manufacturing industry, and the vaccine manufacturing industry.

Many believe that substance exists and is called GcMAF. Its technical names are “group specific component macrophage activating factor” or “Vitamin D binding protein macrophage activating factor.” It is not a miracle drug – it is simply part of the human immune system. GcMAF reportedly activates special cells called macrophages in the human body that have the ability to destroy cancer cells and viruses. GcMAF reportedly also has the ability to treat and often completely cure autism. The connection between cancer and autism is GcMAF.

Nagalase Inhibits the Power of GcMAF to fight Cancer and Autism

The ability of GcMAF to do its normal job can be inhibited by the presence of a protein called alpha-N-acetylgalactosaminidase or nagalase for short. Nagalase is made by all cancer cells and viruses (HIV, hepatitis B, hepatitis C, influenza, herpes, Epstein-Barr virus, and others). [9]

When a person has cancer or a viral infection, the levels of nagalase increase and can be measured to assess the level of cancer or viral activity in the body. [10]

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. [11]

Nagalase and Autism

We also know that the levels of nagalase are elevated in children with autism. What is interesting here is that these children do not have cancer or life-threatening viral infections. In their case, the level of nagalase is elevated and is directly linked to symptoms of the autism spectrum. The result of the immune suppression caused by nagalase is seen in digestive disorders, sensory overload, and numerous types of processing dysfunction in the brain. Higher levels of nagalase are associated with higher levels of autistic symptoms.

Some autistic children do have high viral loads in their digestive system, which would explain the elevated nagalase. However, this is not always the case. 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?

Is Nagalase an Ingredient in Vaccines?

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, and 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. [12]

Were These Doctors about to Reveal the Truth about GcMAF and Nagalase?

Were Dr. Bradstreet and Dr Gonzalez about to explain to the public that one of the key causes of cancer and autism is nagalase, which is being injected into the body as a part of vaccines? [13] Is it possible that those who claim that they are preventing communicable diseases are actually creating cancer and autism? We will likely never know about their plans for disclosure – we can only wonder!

Was Dr. Bradstreet simply so upset over what the United States government did to his clinic that he just got depressed and took his own life? Was he just a quack who was out to fleece the parents of autistic children as the mainstream media suggest? Did he really kill children as some allege? [14]

Dr. Bradstreet was Planning to Make an Announcement about GcMAF

Dr. Bradstreet spoke at the 2015 AutismOne Conference in May of this year. He spoke about GcMAF toward the end of his hour long presentation. He made note of the fact that he had certain important announcements about this therapy that would be released in the near future. Whatever they were, he apparently didn’t live long enough to make them.

During his presentation, Dr. Bradstreet provided an introduction to the therapies that were provided by his clinic, and provided an explanation of how they help restore normal health to autistic children.

He specifically stated:
GcMAF products influence the endocannabinoid pathway. GcMAF has been one of the most powerful tools that I have ever used for autism. How many of you were GcMAF responders and thought it was amazing? How many of you are really pissed off that it is no longer available? I have a little announcement about that coming too. [15]

You may wish to listen to Dr. Bradstreet describe his clinical activities. This lecture was recorded a month before his death. Does this sound like a man who would crumble under pressure from the FDA?

[youtube https://www.youtube.com/watch?v=6I2Wr9ihvV0?feature=oembed]

What about the Other Suspicious Deaths of Doctors?

Various reports from Florida and other U.S. locations reveal that a number of alternative health doctors have been found dead or have gone missing without a trace. These events have occurred during the month that separated the deaths of Dr. Bradstreet and Dr. Gonzalez — June 19th through July 21st. [16]

Disinformation websites have already popped up and have begun to paint pictures in the mind of readers that all this is coincidence and the deaths of these nine doctors had nothing to do with their work. They insist that these events are all unrelated.

The available information about the other deaths is limited. It is hard to judge those situations, because the information about the work of these doctors and their deaths or disappearances is sketchy.

One thing, however, is true – these events create an image in the minds of alternative healthcare providers and their patients that we are entering into a new era of concern, where death may be a real consequence for those who dare to speak out in opposition to big pharma, the dominant conventional healthcare system, and the U.S. regulatory system that is controlled by international mega corporations.

Conventional Media Sources Specialize in Cursing Dead Doctors They Brand as “Quacks”

Conventional media reports of Dr. Bradstreet’s death paint a picture of quackery. They quickly apply the label “paranoid” to anyone who raises questions about the possibility of murder and conspiracy concerning his death and the growing list of dead doctors.

There is clear reason to be concerned. We are now living in an time when the pharmaceutical industry has just about taken total control over the healthcare system, just as the chemical industry has just about seized control over the food supply. How long will it be until the most vocal opponents to corporate domination of healthcare are simply driven out of the United States, or simply silenced under mysterious circumstances? It is a time for alternative minded doctors to become more vocal, and not to be silenced out of fear. It is a time for patients and their doctors to speak the truth about how our conventional healthcare system is killing far more people than it is helping.

A New Day for Health and Healing

There are some people who may not be affected by the nagalase in vaccines. However, for the majority, this substance is suppressing their immune system each time they receive a vaccine. [17] Some infants and children develop autism spectrum disorders as a result, and other children and adults develop cancer.

What would it mean for the call for mandatory universal vaccination of all children if it was understood that vaccinations cause autism spectrum disorder and cancer, and the prevention and treatment of these problems is to stop vaccinating damaged children and to administer weekly doses of GcMAF until they become healthy again? [18]




Notes

[1] “Controversial autism researcher, Jeff Bradstreet, commits suicide after FDA raid in Buford, authorities say,” Joshua Sharpe, Gwinnett Daily Post, 7/26/2015. http://www.gwinnettdailypost.com/news/2015/jun/25/controversial-autism-researcher-jeff-bradstreet/

[2] “GcMAF for the treatment of cancer, autism, inflammation, viral and bacterial disease,” David Noakes, Foundation for Alternative and Integrative Medicine, Retrieved 7/27/2015. http://www.faim.org/autism/gcmaf-treatment-cancer-autism-inflammation-viral-bacterial-disease.html

[3] GcMAF. https://gcmaf.se/

[4] Siniscalco D1, Bradstreet JJ, Cirillo A, Antonucci N.; “The in vitro GcMAF effects on endocannabinoid system transcriptionomics, receptor formation, and cell activity of autism-derived macrophages,” J Neuroinflammation. 2014 April, PMID: 24739187.

[5] Thyer L1, Ward E, Smith R, Branca JJ, Morucci G, Gulisano M, Noakes D, Eslinger R, Pacini S.; “GC protein-derived macrophage-activating factor decreases α-N-acetylgalactosaminidase levels in advanced cancer patients,” Oncoimmunology. 2013 August 1, PMID: 24179708.

[6] “Dr. Gonzalez – Individualized Nutritional Protocols – Enzyme Therapy,” Death Announcement on the website for his clinic. Retrieved 7/23/2015. http://www.dr-gonzalez.com/index.htm 

[7] Suzanne Somers testimony regarding the Death of Dr. Gonzalez, Retrieved 7/27/2015. https://www.facebook.com/suzannesomers/photos/a.10153072450038191.1073741829.55720163190/10153148183048191/?type=1 

[8] “The CIA’s Secret Heart Attack Gun,” Military.com, Retrieved 7/27/2015. http://www.military.com/video/guns/pistols/cias-secret-heart-attack-gun/2555371072001/

[9] “Chapter 9: Nagalase: Friend and Foe?” The GcMAF Book, Timothy J. Smith, MD. http://gcmaf.timsmithmd.com/book/chapter/52/

[10] IBID.

[11] IBID.

[12] Explosive: The real reason Holistic Doctors are being killed and vanishing! https://www.youtube.com/watch?v=cALgIHETMDU

[13] IBID.

[14] “Anti-vaccine doctor behind ‘dangerous’ autism therapy found dead. Family cries foul,” Michael E. Miller, The Washington Post, June 29 2015, Retrieved 7/28/2015. http://www.washingtonpost.com/news/morning-mix/wp/2015/06/29/anti-vaccine-doctor-behind-dangerous-autism-therapy-found-dead-family-cries-foul/ 

[15] “The Bradstreet Essence Protocal,” Dr. James Bradstreet, MD, Presentation from AutismOne Conference, Dated 5/22/2015. https://www.youtube.com/watch?v=6I2Wr9ihvV0 

[16] “2 more MD’s (1 prominent holistic, & one of missing docs) found dead, bringing the total to 8,” Erin Elizabeth, Health Nut News, 7/23/2015. http://www.healthnutnews.com/2-more-mds-1-prominent-holistic-one-of-missing-docs-have-been-found-dead-bringing-the-total-to-8/ 

[17] “Explosive: The real reason Holistic Doctors are being killed and vanishing!” https://www.youtube.com/watch?v=cALgIHETMDU

[18] “Introduction: Routine Nagalase testing finds cancer early and GcMAF cures it” The GcMAF Book, Timothy J. Smith, MD. http://gcmaf.timsmithmd.com/book/chapter/43/

GcMAF & The MHRA: The Persecution of David Noakes and Lyn Thyer

David Noakes is a Guernsey-based British computer consultant, businessman and politician, who founded Immuno Biotech Ltd. to promote Globulin component Macrophage Activating Factor or GcMAF, a revolutionary immunotherapy treatment to remedy conditions like cancer, HIV and autism in direct competition with the globalist-affiliated corporate pharmaceutical industry that wants to sell synthetic "cures" rather than unsaleable natural ones that aren't subject to lucrative patents.

200 scientists have since written over 100 scientific research papers on GcMAF, and Immuno Biotech Ltd have supplied 10,000 people, and achieved fabulous results before the Medicines and Healthcare products Regulatory Agency (MHRA) closed their laboratory down.

20180712-08.jpg

Corruption: These giant pharmaceutical lobbyists influence the legislation of many major Western governments in exchange for generous donations to their sponsored political parties. In return, they are granted various exemptions and legal loopholes that empower their racket at the expense of public health and valuable scientific breakthroughs.

A deadly conflict of interest: MHRA directors Ian Hudson and Gerald Heddell are from Glaxo Smith Kline — the world’s second largest pharmaceutical company. The MHRA protects the monopolies of the multi-billion dollar pharmaceuticals (who can charge around £40,000 for a round of chemotherapy poison) and ruthlessly close down inexpensive, effective treatments wherever it can. Ten public bodies state they are corrupt.

  • For example, Andrew Miller, the chairman of a parliamentary select committee, has said that a “trail of deception” has been exposed in the system.

  • House of Commons Health Select Committee Report of 2005: “In view of the failings of the MHRA, we recommend a fundamental review.”

  • MHRA conceals Seroxat causes suicide: “The MHRA had information in its possession for more than a decade that high doses of the anti-depressant Seroxat (Paroxetine) can lead to aggression and thoughts of suicide. But instead of revealing the truth to the 17,000 people taking high doses and the other half-million Britons on a safer dose, the MHRA sat on its findings. Astonishingly, I was actually threatened with legal action by Professor Kent Woods, chief executive of the MHRA, if I revealed this.”

  • MHRA shreds all its data: Doctor Ben Goldacre, in his book Bad Pharma – Page 80: The MHRA had shredded all its data on the SSRI antidepressants Fluoxetine and Paroxetine (which cause depression and suicide) even though they had seen many scandals with hidden data. Paroxetine was the largest investigation the MHRA had ever conducted; after 4 years criminal charges were considered against its manufacturer, GSK. But MHRA directors Ian Hudson and Gerald Heddell are both from GSK; the criminal charges never happened.

  • The MHRA is GlaxoSmithKline, Aventis Pasteur, Merck, Sharpe and Dohme: A Sunday Express investigation found that nearly a third of the 181 experts who sit on the Medicines Control Agency (MCA, now the MHRA) committees are linked to Glaxo Smith Kline, Aventis Pasteur or Merck, Sharpe and Dohme. The MCA has continued to endorse the triple measles, mumps and rubella (MMR) jab despite concerns linking it to autism and stomach disorders. But the extent of the MCA members’ financial ties to MMR manufacturers raises questions about potential conflicts of interest.

  • Even the courts know the MHRA is corrupt: The MHRA has never successfully prosecuted a company since it was established nearly 10 years ago. (It seems judges won’t accept evidence from so corrupt a source.)

  • The MHRA is infltrated by Big Pharma: “By infiltration, the pharmaceutical companies have taken over completely the regulation of pharmaceutical medicines in the UK. The most powerful of the groups involved is the Medicines and Healthcare Regulatory Agency, (MHRA), like the CDC, the agency responsible for licensing.” Martin Walker, author, Dirty Medicine.

  • The MHRA, the UK Drug Safety Agency, Falsified Vaccine Safety Data – Millions of Children At Serious Risk: Glaxo Smith Kline’s (GSK) Cervarix HPV vaccines for cervical cancer: The MHRA systematically tampered with 6000 reports of adverse reactions to declare the vaccine safe. The MHRA’s Director Gerald Heddell and CEO Ian Hudson are both ex-GSK.


Pharma Protection Racketeering: The MHRA's crime is a £9 billion drug fraud; conspiring to defraud the NHS and the British government of £9 billion, while concealing inexpensive treatments that work, causing 200,000 deaths as a result, the worst kind of fraud.

It's murder for profit. To kill without conscience or remorse requires a psychopathic mentality.



GcMAF has been associated with the successful treatment of 90% of cancers and 50 other diseases, with a reported improved immune response from activated macrophages, lymphocyte availability, and an increased red blood cell and platelet count:




  • All tumorous cancers, which is 90% of all cancers. GcMAF has potent antitumorigenic properties. Treatable cancers include: cancers relating to the neck and head, bladder cancer, colorectal cancer, ovarian cancer, and follicular lymphoma, among others.

  • Autistic spectrum disorders at all ages at an 85% response rate (remedying viruses in the brain and immunological problems that allow them to take hold). Other complications from heavy metals may incur remnant effects that GcMAF does not specifically address. Treating autistic children with GcMAF reportedly diminishes autistic symptoms and improves the endocannabinoid system. Factors required to stimulate macrophage activity are improved in autistic individuals when treated with GcMAF. This treatment has led to improved receptor activity and gene expression.

  • HIV (human immunodeficiency virus). GcMAF's strong suit is in dealing with immunological problems and their offshoot illnesses, HIV is at its root an immunological disease.

  • Improves the Endocannabinoid System. An individual’s health is greatly influenced by the endocannabinoid system and its interaction with the immune system. The endocannabinoid system helps regulate homeostatic processes and is found in organs, glands, and immune cells located everywhere in the body. Individuals with autism have been reported to have altered endocannabinoid pathways and disrupted macrophage defenses. This problem leads to altered immune functioning. These diseases are also associated with improper functioning of the endocannabinoid system: osteoporosis, obesity, multiple sclerosis, Parkinson’s disease, Huntington’s disease, and stroke.

  • Combating the deadly nagalase enzyme. Alpha-N-acetylgalactosaminidase or nagalase is an enzyme found in increased levels in people with autoimmune-related complications (it is also present in mainstream vaccines). Elevated levels of nagalase is associated with an increased risk for lupus, autism spectrum disorders, vital infections such as HIV and AIDS, and many types of cancer. In fact, nagalase has been shown to accumulate in the blood of cancer patients. Its activity shows a strong correlation with the total mass of tumor tissue present in a patient (known as “tumor burden”), as well as how aggressive the cancer is and how quickly it spreads. Interestingly, cancer cells possibly activate nagalase which in turn blocks GcMAF production. Researchers and physicians alike assess the severity of tumors in patients by measuring levels of the nagalase enzyme. Activation of macrophages (the white blood cells that destroy non-healthy cells) is inhibited by nagalase. Nagalase reduces GcMAF through immunosuppression pathways; as a result, the availability of active macrophages is decreased.


[caption id="attachment_17645" align="aligncenter" width="363"]GcMAF-small Nagalese produced by viruses, cancer cells, and bacteria can inhibit natural production of GcMAF, but not GcMAF injected into the body.[/caption]
"Gc-MAF is a promising, new, unapproved medication as a macrophage activating factor (MAF) to treat cancer. There is solid evidence of its efficacy in cancer patients, but a number of researchers remain in doubt. The current study investigated articles containing credible scientific bases to help arrive at a proper conclusion about this product."

Study: Promising role for Gc-MAF in cancer immunotherapy: from bench to bedside.

Yamamoto et al. showed that the administration of Gc-MAF to 16 patients with prostate cancer led to improvements in all patients without recurrence (). Inui et al. reported that a 74-year-old man diagnosed with prostate cancer with multiple bone metastases was in complete remission nine months after initiation of GcMAF therapy simultaneously with hyper T/NK cell, high-dose vitamin C and alpha lipoic acid therapy (). Thyer et al. reported that three men with prostate cancer showed increased nagalase serum levels. About one year after the onset of treatment with GcMAF, they showed a significant decrease in serum nagalase activity (). One study evaluated a decrease in Gc-MAF precursor activity in oral cancer patients with squamous cell carcinoma (SCC) and patients with pancreatic cancer and showed an enhancement of the immune system (). Inui et al. studied cancer immunotherapy with second-generation Gc-MAF (). In addition to Gc-MAF, they administered immune cells, alpha lipoic acid, vitamin C and vitamin D3 alternatively (). Gc-MAF has been verified for use in colon, thyroid (), lung (), liver, thymus (), pancreatic (), bladder and ovarian cancer and tongue squamous carcinoma (). It has also been approved for non-neoplastic diseases such as autism (), multiple sclerosis (), chronic fatigue syndrome (CFS) (), juvenile osteoporosis () and systemic lupus erythematous ().




[caption id="attachment_17644" align="aligncenter" width="491"]hqdefault Pictured from left to right: Lyn Thyer, Ian R Crane and David Noakes.[/caption]

Noakes was imprisoned for 15 months in late 2018 following his guilty plea over four charges of manufacturing, selling, and supplying an unlicensed medicine (GcMAF), as well as one count of money laundering.

The unlicensed medicine, Globulin component Macrophage Activating Factor (GcMAF), is a product manufactured from human blood that was advertised as a cure for conditions, such as cancer, HIV, and autism. The mainstream scientific narrative is that there is no scientific basis for its effectiveness.

Between the years of 2012 and 2015, it has been estimated that Noakes made approximately £7.6 million through sales of GcMAF. It was sold online, through websites across Europe. Around 25% of the produce was given away free of charge to terminal patients, a lot of the remaining income went towards laboratory costs, staff salaries, and travel costs.

Concerns were initially raised in 2015 by the Guernsey medicines regulator, which then led to the Medicines and Healthcare products Regulatory Agency (MHRA) performing an unannounced inspection of the Immuno Biotech’s production site in Milton, Cambridgeshire, UK, where the product was manufactured. During this inspection, it was found that unlicensed manufacturing of GcMAF was taking place; the site, according to the agency, "did not meet good manufacturing practice standards" and the blood plasma raw material being used was "not suitable" for human use.

Please refer to: MHRA Corrupt website.


The MHRA seized more than 10,000 vials of product during the inspection and released a warning for people to not purchase the product, GcMAF; the agency also issued a wanted notice on Noakes. By this time, however, Noakes had already relocated the business to France. In 2017, thanks to a tip off, Dorset police arrested Noakes when he flew into Bournemouth Airport.
“Our investigation team worked relentlessly to bring David Noakes and his associates to justice, for putting public health at risk through the unlicensed manufacturing and sale of GcMAF products. The product was manufactured using blood plasma that was clearly marked as not to be administered to humans or used in any drug products. We strongly advise people not to use unlicensed products such as GcMAF, which may pose a significant risk to health.”

MHRA head of enforcement, Alastair Jeffrey in a Nov. 27, 2018 press statement.

Despite the MHRA's concerns, David Noakes has made it clear that nobody is known to have died due to the use of GcMAF. In fact, GcMAF has saved countless people from the brink of death.



David Noakes' own view on the effectiveness of GcMAF on autism.


Noakes supplied the now dubiously deceased Dr Jeffrey Bradstreet who was involved in using GcMAF to a supposed 85% varying response rate. Bradstreet was found dead three days after his clinic was raided by the FDA having allegedly "shot himself in the chest" on June 19, 2015.

Q: So you're saying there's an 85% response rate for autistic children treated with GcMAF?


Noakes: Well, it all came as a bit of a shock to us as we hadn't realized that autism was simply viruses in the brain and viruses in the stomach. Dr. Jeffrey Bradstreet contacted us asking to use GcMAF to treat autism, and we weren't convinced that it would help, but nonetheless, as it's a free world, we shipped it out to him. 16 weeks later, he called again to say he'd had full recoveries and has now treated over 700 children with First Immune GcMAF. We now have a total of four clinics that have used our GcMAF to treat just about 1000 autistic children now. We get wonderful emails from the parents of these children saying 'thank you so much for giving my child back to me'. It's wonderful to have something which is 85% successful because you don't often get a response rate in medicine that high.

Q: What improvements are you seeing with these children, when they're treated with GcMAF?


Noakes: Well, it's cognitive abilities; it's the recognition of shapes and colours — it's the ability to speak fluently. These children are getting from a point where they are virtually unable to communicate and can treat their parents terribly badly, to becoming normal friendly children who love their parents. 

Q: Has GcMAF been trialed in young adults with autism?


Noakes: Well, we have a 21-year-old who used to awaken with violent screaming and aggression — and over a period of twelve weeks (of GcMAF) that completely disappeared, and he's leading a much more normal life. There are approaching a thousand children that have been helped by GcMAF, but there are too many cases to go through all of them.

Q: Will this mean fewer autistic children will be institutionalized?


Noakes: Well, this is the beginning of the end of the autism disease. Forever. We know it's the immune system that can eradicate it. We know how to rebuild the immune system. With an 85% response rate, we are very close indeed to giving huge numbers of parents and their children a completely new lease of life and happiness.




Where to Find GcMAF ImmunoTherapy

As expected, GcMAF immunotherapy is not available commercially in the U.S. and the FDA considers it an unapproved drug. This is one of the major reasons why Dr. Bradstreet’s clinic was raided by the FDA.

There are still some clinics that offer GcMAF immunotherapy, but due to obvious concerns, most don’t advertise this. A medical organization in Japan, called Saisei Mirai, has manufactured and tested both a serum form of GcMAF that is injected into the patient, along with an oral bovine colostrum form. Products can be purchased from their website.

Colostrum and GcMAF

Colostrum is a form of first milk produced in mammals (including humans) that contains high levels of immunoglobulins designed to help build the newborn immune system. Specific types of bovine colostrum derivatives have been shown to be GcMAF activators. Colostrum has been shown in studies to activate GcMAF in individuals with serious infections and fatigue.

High quality colostrum is obtained from grass-fed cows or goats and comes in a capsule or powder form. It does contain small amounts of dairy proteins such as casein and whey, but due to the immunoglobulin matrix it is most often well-tolerated by people who are sensitive to dairy products.

It is best to consume colostrum away from meals to allow for quicker passage through the stomach to the gut. Swallowing pills may be the easiest approach, but the most effective may be swishing the powder in your mouth. In the mouth and throat there is specific immunological lymphoid tissue which is typically rich in macrophages. You can take a colostrum powder with water and put it in your mouth for 15-20 minutes to help activate these macrophages and absorb immunoglobulins sublingually.

After 15-20 minutes, swallow the mixture. This is one of the most effective ways to boost macrophage activity and is a recommended method for individuals who suffer with immunoglobulin deficiency syndromes.

Bravo Yogurt and GcMAF

Bravo yogurt is not available in stores. The starter culture must be ordered online and prepared at home.

Dr. John Gray has this to say about Bravo Yogurt on his website: “Bravo Yogurt has proven to produce GcMAF in a completely natural way. This GcMAF Probiotic Bravo Yogurt Kit contains 42 essential probiotics to restore healthy gut function and digestion. These 42 strains of probiotic bacteria have proven to produce the essential protein, GcMAF.” 

One special type of yogurt is now being marketed for its benefits on activating GcMAF. This yogurt is called Bravo Super Probiotic Yogurt and it’s not available in grocery stores so it must be ordered online and prepared at home.

The typical daily recommendation goes like this: Take a half cup of the special Bravo yogurt in the morning or at the end of a fiber-rich meal. After consuming the yogurt, don’t eat or drink anything for an hour to make sure the probiotics and immunoglobulins avoid increased digestive activity and are able to get into the system.

With every spoonful it is recommended to swish it in your mouth for 30-60 seconds and then gargle it before swallowing. This helps to get the immunoglobulin compounds into the lymphoid tissue in the mouth and throat.

How to Boost Your GcMAF Levels

Healthy individuals are believed to produce approximately 10,000 cancer cells each day. GcMAF aims to destroy these cancer cells. Therefore, it is critical for you to maintain GcMAF concentration levels in your body in order to promote health and optimize the full healing capabilities your body has to offer.

Olive oil and avocados are good sources of oleic acid.

Individuals taking GcMAF are encouraged to use oleic acid in the form of olive oil and avocados along with supplementing with high doses of vitamin D3. Drinking a minimum of 2 liters of water and herbal teas each day is also recommended. You should also consume a low carbohydrate, ketogenic style diet high in good fats and key proteins shown to slow the development of cancer.

If you consider yourself a relatively healthy person already, minimize your risk of developing chronic disease or cancer by choosing a healthy lifestyle.

Lifestyle Recommendations to Reduce Your Risk of Cancer

There are specific things you can do to support your body’s natural abilities to increase GcMAF production and optimize your health. Build a strong immune system by using the following recommendations as a guideline:

  1. Limit your sugar consumption. Physicians are increasingly becoming aware of the health threats which sugar promotes. Not only should you avoid simple sugars such as sweets, but also complex sugars which are broken down from starches and grains. Both types of sugars feed cancer cells and need to be limited in your diet (and preferably eliminated).

  2. Receiving adequate amounts of vitamin D3 daily is required for optimal health. One of the leading causes of autoimmune complications is vitamin D deficiency and may lead to a variety of concerns such as autism and cancer.

  3. Avoid soy milk which may limit the absorption of trace minerals.

  4. Eliminate all forms of wheat from your diet along with cancer causing agents such as lectins.

  5. Carrageenan is an additive found in a variety of foods which should be avoided at all costs. Carrageenan is used as a thickening agent and has also been found to block GcMAF activity. You may find it useful to think of the effects of carrageenan as similar to the nagalase enzyme which ultimately is responsible for weakening immune defenses.

  6. Avoid the need for a root canal and when possible, choose a tooth extraction. Root canals are associated with the destruction of the immune system.

  7. Avoid any substance which suppresses the immune system including cortisone, steroids, and anti-inflammatory drugs. This advice is from a specific treatment plan offered by the Immunocentre of Europe* for naturally stimulating GcMAF production. Their treatment protocol also recommends the avoidance of radiation therapy and all experimental drugs which may cause adverse health effects and unknown reactions. [*Editor’s note: since this article was written, the Medicines and Healthcare products Regulatory Agency (MHRA) in Britain has closed down this company.]

  8. Remove all artificial sweeteners from your diet. Sugar substitutes such as aspartame suppress the immune system. Opt for plant-based sweeteners such as Stevia or Xylitol made from hardwood (not corn).

  9. Reduce your stress. People who have been diagnosed with cancer or a chronic disease might readily recall a recent life-changing occurrence which resulted in a severe shock to their bodies. Reducing stress levels is absolutely necessary to building a strong immune defense. Stress has the ability to puncture holes into your titanium-armored immune defenses and consequentially allows disease a chance to take hold.

  10. Consume a diet rich in fish, pastured, grass-fed meat, and a variety of vegetables to optimize nutrient intake. Diets lacking essential amino acids and trace minerals result from poor nutrition and can lead to the degradation of your health and reduced GcMAF concentration. Consuming an optimal diet of organic vegetables and pastured, grass-fed meat and wild fish will help keep GcMAF levels high.

  11. Move your body. Lack of oxygen and exercise are two of the most important factors associated with the development of cancer. The circulation of oxygen and exercise does more than benefit a healthy figure. Cells rely on a steady supply of oxygen to function properly.


Exercise optimizes health by promoting factors which reduce your risk of cancer. For instance, exercise limits the flow of cortisol through your body which causes stress and anxiety. Specifically, increased cortisol levels in men are associated with a decline in testosterone levels and are a risk factor for heart complications.

  1. Avoiding environmental contaminants is recommended to reduce the toxicity of your immune system. Eliminate all toxic habits such as smoking which lead to carcinogenic mutations and put you at an increased risk for chronic ailments.






Are Benefits of GcMAF Purposely Being Hidden from the American Public?

GcMAF has shown incredible promise in the treatment of cancer, autism, and many other chronic diseases. Unfortunately, the FDA appears to be acting to suppress this information and terrorized one ofthe leading experts in Dr. Jeff Bradstreet. Could Dr. Bradstreet even have been killed over his use and expertise in GcMAF? Or was it really a case of suicide, likely brought on by the stress he must have endured from the threat of arrest and imprisonment for promoting an alternative treatment?

We will have to wait until all investigations are final, and of course, we may never know the truth. In the meantime, you can begin receiving some of the benefits of GcMAF therapy by using a high quality bovine colostrum supplement and vitamin D3, along with a low-carb, ketogenic style diet, and an active, healthy lifestyle.

Wednesday, 15 May 2019

How to Save Your Toxic Brain

From Myers Detox.

41 million IQ points.

That’s what Harvard Medical School professor, Dr. David Bellinger, estimates Americans have collectively lost because of exposure to lead, mercury, and organophosphates, the most common pesticides used in agriculture.

Today I want to talk to you about how to save your toxic brain.

When toxins are allowed to enter the brain and central nervous system, they can cause a whole host of symptoms.

Many of you suffer from brain fog, brain fatigue, trouble staying focused, forgetfulness, mood swings, or you fear dementia as you age.

  • Anxiety

  • Slow processing of new ideas

  • Sadness

  • Impatience

  • Irritability

  • Lack of motivation

  • Cognitive decline


I guarantee many problems incorrectly attributed to a host of other things are in most cases actually caused by body burden toxicity.

I want to explain the exact mechanisms of how toxins enter the brain.

The blood-brain barrier tries to protect our central nervous system from exposures to compounds that may be inflammatory and interfere with homeostatic mechanisms that maintain neurotransmitter balance and nervous system functioning.

But when we are chronically exposed to toxins and contaminants, like we are in today’s modern world, the usually tight and very selective blood-brain-barrier begins to warp under the pressure of these inflammatory compounds and becomes a bit “leaky” so that it allows molecules through that would have otherwise been prevented from entering the compartment that encases our brain.

This is what’s called Leaky Brain.

Metals that poison our mitochondria are also contributing to leaky brain.

Our brain uses 20% of the energy produced by our bodies.

In fact, another Harvard professor, Dr. Philippe Grandjean, warns of a “silent pandemic” of neurotoxins destroying our brains.

Your brain may be polluted with mercury, arsenic, chlorpyrifos, PCBs, ethanol, and other neurotoxins that stop it from performing at its best.

Mercury 

  •  Deposits in the pituitary – the master gland controlling all your hormones

  •  Inhibits nerve cell formation

  •  Block melatonin receptors needed to have a good night’s sleep

  •  Contributes to dementia like Alzheimer’s and developmental disorders like Autism


Lead

  • Impairs learning and memory

  • Associated with chronic fatigue, depression and cognitive impairment

  • Destroys energy production, needed for brain function


Aluminum

  • Kills brain cells

  • Causes brain inflammation


These neurotoxins and thousands more are poisoning our brains.

They’re lowering our IQs.

They’re causing an explosion in ADHD and autism spectrum disorders in our children.

And because of widespread environmental toxins we’re ALL at risk.

My life’s work is dedicated to helping people remove toxins from their body.

I developed a powerful new way to detox your brain, bones, fat, and central nervous system. Click here to learn more.

dsada




Further notes:

  • Alternatively, I would recommend the Andy Cutler Chelation Protocol for mercury, once the mercury is removed, aluminium tends to leave the body too. The ACC protocol accounts for the dangers of heavy metal redistribution in tissues during the excretion process.

  • I'd also recommend high silica water to help remove aluminium during the ACC protocol.

  • Carbon 60 (C60) is also a viable option for safely removing metals from the body and brain.

Tuesday, 14 May 2019

Have The British Royal Family Interbred With Jews?

From Inspire Change World & Alma.

For the last few years, I have been telling people that the British “Royal Family” are absolutely not as they seem. […] I have said that these people are absolutely not British in any aspect, but are criminals, frauds, and have absolutely no rights to the British throne at all..

Now, I want to reveal through an article from my friend, Whitewraithe, who writes the blog: Pragmatic Witness, that amazing article, entitled: “Britain’s Jewish Royal Family” right here for everyone to see for themselves, and I do, of course, have some additional thoughts and comments to follow:

Britain’s Jewish Royal Family


What we have been sold is no less than the groundwork for the imposition of a future Jewish Monarchy in Great Britain. And engineered by the House of Rothschild, whose relations and puppets on Wall Street and in the City of London are responsible for a deliberately created international financial crisis aimed at creating a one world currency system, a one world bank and a New World Order, one world government.

As one Royal insider commented “An insecure immigrant Royal family who have never felt at ease with the British people, and always more secure with immigrants and outsiders, and an alliance with the richest Jewish family in the world, heads of what is increasingly being re-Christened “The Jew World Order, who also seek to raise their status, is perceived by the Queen and the Duke of Edinburgh as the best guarantor of their family’s future and safety. In short, we will one day see a Rothschild Royal family.”

Many people still cannot get Kate Middleton or why she, a supposed ‘commoner’ would marry Prince William. But hidden right under our noses is the truth the controlled mainstream media is hiding. Kate Middleton is a Jew from a maternal line of non-practicing, assimilated and poor Sephardic Jews aligned to the Church of England. Her mother whose maiden name is Goldsmith, practicing or not, is Jewish and under Jewish law if the mother is Jewish then the children are Jewish, therefore the children of Prince William will be legally Jewish….especially as William, under Judaic law, is also a Jew!
Under Jewish law if William and Kate have children their children will be Jews!

Princess Diana was a Jew because her mother was a Jew therefore Princes William and Harry:  See also: Huffington Post — A Jewish King And Queen Of England? It’s Possible

PRINCESS DIANA’S PARENTAL JEWISH LINEAGE:


In Tina Brown’s book ‘The Diana Chronicles’, the author claims that Princess Diana’s Jewish mother Frances Shand Kydd had a long-running affair with Sir James Goldsmith during her marriage to Earl Spencer. She suggests that Diana, who was born in 1961, was Goldsmith’s love child and not Spencer’s daughter. Even so the father’s line is irrelevant as Jewishness travels down the matriarchal line and Diana’s mother was a Jew. See also:  The Times of Israel —  Will the Future King of England Be Jewish?

The Goldschmidts, like their neighbors and relatives, the Rothschilds, had been prosperous merchant bankers in Frankfurt, Germany since the 16th century.(Wikipedia). In 1773, Mayer Rothschild invited Goldschmidt, (Goldsmith), Schiff, Oppenheimer, Warburg and eight other ambitious Jewish businessmen to his goldsmith shop. Together they formulated a long term plan […].

PRINCESS DIANA’S JEWISH SON AND FUTURE KING WILLIAM.

The original and current Jewish definition of a “born Jew” is a person whose mother is Jewish. Judaism is passed down in a matriarchal lineage. Prince William’s mother, Princess Diana, had a Jewish mother (Frances Ruth Burke Roche; a Rothschild) and she likely had a Jewish father (though his lineage would be irrelevant under Jewish law). That would make William – Jewish.

PRINCESS DIANA’S JEWISH HALF-BROTHERS


Diana shares a striking physical resemblance to the children of Sir James Goldsmith – Zak Goldsmith, Ben Goldsmith and Jemima Goldsmith. They are allegedly Diana’s half brothers and sister.

Following the Rothschild protocol of interbreeding to keep the power and wealth all-in-the-family, Diana’s alleged half brother Ben Goldsmith wed Kate Rothschild in 2003.

Princess Diana’s other alleged half brother, Zac Goldsmith, divorced his wife after he was elected British MP. He is now living with Alice Rothschild. This Rothschild-Goldsmith couple is also expected to marry.

Many people were perplexed why parliament should — recently, during one of it’s most busy sessions since the war –, have enacted a law allowing Catholics to ascend to the throne. What perplexed them was that the issue was not even on the horizon and there was simply no justification at that stage to use valuable parliamentary time dealing with it. In the light of this theory we can better speculate what was going on.  This was an ‘en Passant’ means of allowing Jews to take the throne on the basis of the ‘equality’ and ‘diversity’ our cultural Marxist Queen so greatly cherishes.

People have also always been mystified why Charles married Diana in the first place given that he was deeply in love with and had a long-standing relationship with Camilla Parker-Bowles. But that marriage made perfect sense if the family simply wanted Jewish children for a future Jewish monarchy. Whether the relationship lasted or not was of little importance once the the children were born and how convenient that Diana went the way of a wife of Henry the Eighth.

But the Kate-William marriage also perhaps explains Prince Charles’s dictum that, should he be ruler, he would seek a constitutional change that would remove him from sole governance of the Church of England to become the leader “Of all faiths.” Such a constitutional move would give Judaism parity with Christianity allowing a Jewish member of the Royal Family, for example, even if it were a woman, to ascend to the throne […].

And so the Rothschilds attended the royal wedding in more ways than one!

THE PLAN WAS THERE ALL ALONG, IN FRONT OF OUR UNCRITICAL, BRAINWASHED EYES

COMING OF THE MESSIAH.


However, the Talmud states that the leader of the world Jewish takeover would be a King, meaning that, should a male Jew ascend to the throne, such a King would then himself not only be the senior Elder of Zion but also the long awaited Messiah; The King of the Jews. As there are no remnants of the ancient Jewish royalty, and in order to fulfill the prophesy, Jewish royalty must be re-established, and it appears from this evidence that the current British Royal family has become the vehicle of choice.

At last, we come to understand the old Masonic claim that “Jerusalem will be rebuilded here, in England’s green and pleasant land.” The King of the Jews will rule the world from London where the ‘square mile’ of London City no longer belongs to the English people but was long ago sold to the Jews. His castle may well sit on the site of the last Olympic games; an area stolen by the state from the East Londoners who lived and worked there, perhaps in the long term for this very purpose.

Could the New Jerusalem be built in the ‘square-mile’ or could it be built on the Olympic site which was surrounded during the event by the Jewish and Masonic symbol of triangular, pyramid floodlights? Could the arena of the Olympic stadium become the site for the rebuilding of the temple? […]

On a related point, Royal rumour has it that Prince Harry was under great pressure, especially from the Queen, to marry Meghan Markle to help promote the racial genocide of the indigenous British people through mass immigration, cultural Marxism and Zioncorp promoted miscegenation.

A series of Jewish and far-left MPs such as Margaret Hodge, using mass third world immigration and fixed housing lists in the East End, have already succeeded in almost wiping out the Cockneys in this effort.

The Queen famously threatened in her 2010 Christmas Speech “The future face of Britain is the face of the Commonwealth.”

i.e.: The end of the white race in the United Kingdom!