reducing agent.
aka Kunyit, Yellow-root or Geelwortel.
Worldwide, the use of Turmeric is said to have healing properties for brain related diseases such as Alzheimer and Parkinson ( hardly found in India). The beneficial properties of Turmeric are also being investigated by Cancer Research Institutes.
The Healing Power of Turmeric - and powerful cancer killer
It has been shown before that curcuma/kurkuma or turmeric is good for losing weight and it’s beneficial for your memory. Now it is supposed that curcuma also has the power to kill cancer cells.Scientists of the Cork Cancer Research Center in Ireland have discovered that the Indian yellowroot is capable of breaking down cancer cells.The team under the lead of Sharon McKenna found that cancer cells started to die 24 hours after they had come into contact with curcuma. Furthermore it was shown that cancer cells started to dissolve themselves after this.Previous studies have shown that curcuma reduces the growth of fat cells, making you gain less weight. Other scientific research has shown that curcuma also protects against dementia as well.All studies were laboratory studies. Further research needs to shown if curcuma has the same beneficial effects in humans. However, my personal experience with Kurkuma to treat skincancer are positive. A spot on my back, just between the shoulderblades, over 3 inches in diameter, allmost disappeared within 2 weeks after using the powder....( direct contact by rubbing it on the skin). Almost on a daily base I add kurkuma, cayenne and ginger to my meals for about a month now. My skin seems to be juveniled, little wraths on my hands are gone...
Curcuma, turmeric or Indian yellowroot is a much used spice in the Indian kitchen. It has a yellow color and a slightly bitter taste.
Turmeric is one of nature's most powerful healers. The active ingredient in turmeric is curcumin. Tumeric has been used for over 2500 years in India, where it was most likely first used as a dye. The medicinal properties of this spice have been slowly revealing themselves over the centuries. Long known for its anti-inflammatory properties, recent research has revealed that turmeric is a natural wonder, proving beneficial in the treatment of many different health conditions from cancer to Alzheimer's disease.
1. It is a natural antiseptic and antibacterial agent, useful in disinfecting cuts and burns.
2. When combined with cauliflower, it has shown to prevent prostate cancer and stop the growth of existing prostate cancer.
3. Prevented breast cancer from spreading to the lungs in mice.
4. May prevent melanoma and cause existing melanoma cells to commit suicide.
5. Reduces the risk of childhood leukemia.
6. Is a natural liver detoxifier.
7. Prevent and slow the progression of Alzheimer's disease by removing amyloyd plaque buildup in the brain. Likewise for Dementia. Improves memory.
8. Prevent metastases from occurring in many different forms of cancer.
9. It is a potent natural anti-inflammatory that works as well as many anti-inflammatory drugs but without the side effects.
10. Has shown promise in slowing the progression of multiple sclerosis in mice.
11. Is a natural painkiller and cox-2 inhibitor.
12. Aids in fat metabolism and help in weight management.
13. Has long been used in Chinese medicine as a treatment for depression.
14. Because of its anti-inflammatory properties, it is a natural treatment for arthritis and rheumatoid arthritis.
15. Boosts the effects of chemo drug paclitaxel and reduces its side effects.
16. Promising studies are underway on the effects of turmeric on pancreatic cancer.
17. Studies are ongoing in the positive effects of turmeric on multiple myeloma.
18. Has been shown to stop the growth of new blood vessels in tumors.
19. Speeds up wound healing and assists in remodeling of damaged skin.
20. Helps in the treatment of psoriasis and other inflammatory skin conditions.
21. When the body is poisoned by Cyanide, Lead or Cadmium it will be neutralized.
22. It induces Chemokines to migrate to inflamated spots.
23. Helps to prevent Thrombosis.
24. Prevents and kills Colon-cancer (Crohn).
25.Diabetes patients will benefit from the healing power of Kurkuma.
26. It is a woundhealer, fights pimples, helps against various types of swellings and insect stings,
27. Leprosy,
28. Dropsy click29. Liver cancer, click. Studies have shown that turmeric has anti-tumor, anti-oxidant, anti-arthritic, anti-ischemic, and anti-inflammatory properties. In addition it may be effective in treating malaria, prevention of cervical cancer, and may interfere with the replication of the HIV virus.
Next to the yellow root there's a black variant:
Black Turmeric is a herb with bluish-black rhizome,native to North-East and Central India. The leaves have a deep violet-red patch which runs through the length of the lamina. Usually, the upper side of the leaf is rough, velvety, but this character may vary. Flowering bracts are green with a ferruginous (iron) tinge. Flower petals may be deep pink or red in color. The rhizome is bitter, hot taste with pungent smell. Black Turmeric is used in Tantrik Sadhana. The dried leaves are used as a source for fuel. Northern tribes use Black Turmeric as a talisman to keep the evil spirits away. Presently Black Turmeric is on the verge of extinction due to unfavorable climatic changes, deforestration, soil erosion and bio-piracy
It's benefits?
1. Hemorrhoids,
2. Leprosy,
3. Bronchitis,
4. Asthma,
5. Cancer,
6. HIV/Aids,
7. Epilepsy,
8. Fever,
9. Wounds,
10. Impotency,
11. Fertility,
12. Menstrual disorders,
13. Toothach,
14. Vomiting,
15. Piles
http://bert-firebert.blogspot.com/2010/08/healing-power-of-kurkumaturmerec.html
…
lic believes these vaccines, aside from their specified virus(es), are sterile solutions, free from undesirable contaminants not listed on the manufacturer’s package inserts. When the pediatrician injects a vaccine into the muscle of a child, the public has unquestioning faith that this is the case. In other words, we want to believe that vaccines have been generated under perfect conditions for the safety of children and ourselves.
Our investigation shows that most people do not know what is actually in a vaccine: the active ingredients listed on product labels, inert ingredients, and, most important, the hidden ingredients. Even more remote is taking the time to actually study the subject matter, review the scientific literature and discover the truth for oneself. To our amazement, that truth was easy to find. But it is a truth that will scare the hell out of you.
Similar to eating veal parmesan, what would happen if a video were placed on your table and used as a living reality recipe instead of the actual meal. This video unfolds before your eyes every step in that little creature’s life, from the veal’s birth to the parmesan on your plate. You witness how this veal was starved of its natural nutrients, kept in a tiny stall, grossly malnourished and deformed, filled with drugs—antibiotics—diseased and suffering complete privations until finally slaughtered, sliced, cooked and served on your plate. Would your appetite be the same? Would you still desire the parmesan? Conveniently we rarely ask the questions, where does our food come from? How and where was it grown? What was sprayed on it prior to our consumption? Therefore, we are going to re-record something that even most top health educators and opinion leaders on vaccines are unaware of. That is, what goes into the making of vaccines and what is hidden from you that should give you a moment’s of pause? Then ask yourself, do you want vaccines in your body?
To give us the most in depth, honest, scholarly and objective examination about the methods by which vaccines and their hidden ingredients are prepared we turn to the award-winning British investigative medical journalist, Janine Roberts, who paints an entirely different picture about the darker inferno in vaccines that do not appear on product labels. This is the same Janine Roberts who brought to the world’s attention blood diamonds, genocide in the Congo and the destruction of aboriginal cultures by the Australian government.
Roberts’ account of conversations between high level members from the World Health Organizatioin (WHO), federal health agencies, and expert vaccine scientists, who determine whether or not a certain vaccine will be approved or not, is horrid. Her investigations are based on official meeting documents and her attendance at emergency vaccine meetings, and confirm that our world’s vaccine and health experts agree there is no solution in sight to resolve the potential and uncertain threats posed by these hidden ingredients.(1)
The story begins with the vaccine industrial complex’s attempt to reduce vaccine manufacturing costs by seeking government approval to use cancerous cell lines in the development of vaccines. Vaccine industry’s rationale is that cancerous cells are “immortal.” Current vaccine methodology relies on animal cells, such as fertilized hen embryos and monkey kidneys, that die quickly in culture. Using cancerous cell lines are also much cheaper than relying on the purchase of animals, especially monkeys, that need to be sacrificed for vaccine substrates.
Roberts records two separate meetings—a meeting of the Vaccine and Related Biological Products Advisory Committee on November 9, 1998, and a subsequent gathering of the Evolving Scientific and Regulatory Perspective Workshop less than a year later. The conversations were conducted at a scientific level between top officials and expert scientists from the FDA, Centers for Biologics Evaluation and Research (CBER), the National Institute of Allergies and Infectious Diseases (NIAID), the WHO and others, each providing evidence and/or confirmation that all vaccines are dangerously contaminated.
Conversations focused primarily on the influenza, MMR and yellow fever vaccines, which rely on fertilized chicken eggs for their culturing viruses. Fertilized chicken eggs, while ideally suited for culturing certain viruses for vaccines, such as the influenza and MMR vaccines, are also living incubators for large numbers of known and unknown viruses in the animal kingdom. While these do not transmit from their animal host to humans naturally, they nevertheless are sequential genetic codes, which when injected into the human body, have the potential for any number of unpredictable adverse effects by interfering or merging with the codes of human cells. Vaccine research is at best a primitive science because it is injecting into the blood stream foreign substances, chemical and genetic, that would otherwise not enter the body naturally. When we include into the equation the enormous amount of known and unknown genetic material and foreign proteins that vaccines introduce into the body, and then consider the rapid increase in epidemics raging across the American population—adult diabetes in children, large numbers of various inflammatory and immune deficiency diseases, asthma and new allergies, severe gastro-intestinal disorders (eg., leaky gut syndrome and Crohn’s Disease), chronic fatigue syndrome, and many different neurological disorders (eg., autism, ADD and ADHD, Parkinson’s, Alzheimer’s, etc.)—we must step back and reconsider their causes. We should avoid the kind of faith the vaccine industrial complex has in its determinist, reductionist perspective of genetic materialism to find these answers without taking into account the bombardment of toxic chemicals such as vaccine adjuvants and preservatives, extraneous genetic material, and pathogenic organisms and foreign genetic fragments that we assault our bodies from shortly after birth into old age.
For some time, it was known that the enzyme reverse transcriptase (RT) was present in final vaccine solutions. RT has been used to this day as an indicator that there is a presence of a retrovirus. During the meeting’s proceedings, the WHO decided to withhold public announcement of such genetic contamination, in this case concerning the MMR vaccine, and made the decision to not remove it from the market and, in the meantime, continue safety studies at various laboratories.
Roberts reports that Dr. Arifa Khan from the FDA confirmed:
The RT activity in the vaccine was associated with retrovirus particles from two separate viral strains: Avian Leuokosis Virus (ALV) and Equine Arteritis Virus (EAV). The former was especially disturbing because ALV is a leukemia cancer, and Dr. Khan stated: “There was a theoretical possibility that the virus [ALV] could… infect the [human] cell.” In summary, this means the ALV genetic code could integrate with human DNA, hence causing some kind of cancer.
The FDA’s reassurance that the ALV RT activity was safe is based on laboratory observations that there was no viral-human DNA merger activity for “a full 48 hours’. This kind of assurance is almost nonsensical and flies in the face of scientific reasoning since cancers can take years to develop!
As a side note, reverse transcriptase activity is one of the stalwarts of the HIV/AIDS hypothesis. An article, “Serious Questions Regarding the Safety and Efficacy of the Influenza Vaccine” published by Canada’s Vaccine Risk Awareness Network reports that some studies, and even some vaccine package inserts, “indicate that vaccinations increase HIV viral replication.”(2) This means all vaccines stimulate a strong suppressive effect on the immune system. Under stress conditions, viruses turn hyperactive and increase their ability to replicate.
The other risk stated by the FDA official was the possibility of the ALV sequence merging with the measles virus, hence creating a completely new, mutant and dangerous virus. (This could also apply equally to the H1N1 swine flu and any other flu vaccines). As an aside, the world renown British geneticist Dr. Mae-Wan Ho from the Institute of Science in Society wrote that, “Vaccines themselves can be dangerous, especially live, attenuated viral vaccines or the new recombinant nucleic acid vaccines, they have the potential to generate virulent viruses by recombination and the recombinant nucleic acids could cause autoimmune disease.”(3)
During the meeting, Dr. Andrew Lewis, then head of the DNA Virus Laboratory in the Division of Viral Products confirmed that “All the egg-based vaccines are contaminated…. These fertilized chicken eggs are susceptible to a wide variety of viruses.” The participants also realized that only a very small fraction of these small contaminants have been identified and there are likely hundreds more to be discovered.
Roberts found a 2001 CDC report showing that RT investigative studies for both the ALV and EAV retroviruses were conducted in 100 patients receiving the MMR vaccine. They found undesirable “RT activity in all measles vaccine lots from different manufacturers tested.” Their conclusion is that “this occurrence is not sporadic and that vaccine recipients may be universally exposed to these [chicken] retroviral particles.” In a separate National Institutes of Health transcript of a meeting, Dr. Conroy of the World Health Organization stated that EAV viruses are found in all fertilized chicken eggs. There appears to be little change in the scientific protocol for making the influenza, MMR and yellow fever vaccines. The current release of intramuscular H1N1 vaccines for the global market relies on the use of fertilized chicken embryos. These include each of the approved vaccines by CSL, Medimmune, Novartis and Sanofi-Pasteur, as well as GlaxoSmithKlines if and when it is approved in the US.
A late meeting of the FDA’s Scientific and Regulatory Perspective Workshop, without the press, was convened on September 7, 1999 in Washington DC, and attended by “representatives from all the largest public health institutions in the West.” The following are summaries of key points and statements raised during this meeting as recorded in Janine Roberts invaluable book Fear of the Invisible.
It was reconfirmed that vaccines are “widely contaminated by viral and DNA genetic code fragments, many viruses and proteins. There was expressed concern that these may also contain prions (tiny proteins responsible for incurable diseases and neurological disorders in both humans and animals) and oncogenes (a gene that turns normal cells into cancerous ones). One attendee, Dr. Goldberg, stated, “There are countless thousands of undiscovered viruses, proteins and similar particles. We have only identified a very small part of the microbial world—and we can only test for those we have identified. Thus the vaccine cultures could contain many unknown particles.”
Dr. Andrew Lewis of the FDA said that a brand-new monkey-human mutant virus was created during the course of creating an adenovirus vaccine with adenvovirus-SV40 hybrid viruses. Dr. Lewis also worried that “foreign cellular DNA” common in childhood vaccines could include “viral oncogenes” capable of causing cancer.
The scientists presented a question to themselves as to whether or not an attenuated vaccine strain could revert into a variant virus capable of replicating so fast that it would cause AIDS. They agreed that they were unable to answer this question.
On the question whether or not mutation events could occur in children after vaccination, the answer was that “Recombination among a variety of viruses [contaminant viruses] and cells co-infected in tissue culture is not uncommon.” What this basically means is that because it is “not uncommon” for genetic codes of both contaminant viruses and living cells to recombine and create mutations in laboratory cultures, it can certainly occur in a child’s body after vaccination.
Dr. Hana Golding, Chief of CBER’s Laboratory of Retrovirus Research, raised the fear that although DNA fragment contaminants in vaccines may be thought to be dead, they could remain active and dangerous. This meant that the codes of these contaminants could combine in vaccines and create new mutant strains of pathogens.
Dr. Leonard Hayflick, a virologist at both Stanford and the University of California at San Francisco raised a concern that the common primary culture used for making vaccines with animals and bird embryos has created a situation where it is “apparent that these cells contained many unwanted viruses, some of which were lethal to humans.” This was especially worrisome of those vaccines, such as polio, which still relies on monkey kidney cells that have contributed to widespread death and illness.
One of the UK’s leading vaccine expert, Dr. Phil Minor from the National Institute of Biological Standards and Control, noted that some cases of polio vaccine are polluted with more monkey virus, SV40, than actual poliovirus. Although the uninitiated who are not informed about-closed door vaccine science have been led to assume that SV40 was no longer in polio vaccines at the time of this meeting, the conversations confirmed that it was still in use. This is another example of deception at high levels within the vaccine industrial complex and high government health officials to withhold information that directly impacts the health and well being of citizens.
Dr. Rebecca Sheets from the CBER’s laboratory responsible for monitoring vaccine safety stated the national health organizations had no control over how vaccines were made. In short, they could make recommendations but the vaccine industrial complex was free to act as it choose.
It is impossible to remove DNA contaminants from vaccines. Although weight limits for contaminating DNA were set by the FDA as far back as 1986, vaccine makers have never been able to reach that goal. The CDC decided to limit their weight recommendation to cancerous cell lines and then increase the other DNA contamination allowance one hundred-fold. However, these limits are only “recommendations” and, therefore, the FDA is unable to enforce them. Vaccine manufacturers continue to have the freedom to take scientific measures to reduce contaminants only if they wish.
Remember, this level of contamination (10 nanograms) only applies to a single vaccine. Children today are inoculated with many vaccines before entering school, each with unique DNA and viral contaminants due to the specific cell substrates used for a given vaccine. This toxic genetic soup is what then flows through a vaccinated person’s body.
One government health official stated, “I chaired the committee that licensed the chickenpox vaccine, and it [residual DNA] was actually an issue that we considered at that time. We looked among recipients of the vaccine for evidence of an autoimmune response associated with the DNA included in that vaccine…… Actually, we didn’t look, we asked the company to look and they did not find one.” Well, of course, only such assurances can be convincing if in fact the company conducted the study, for which there was no compulsory reason to. Clearly, what the official is saying is that health authorities do not possess any study documents that such a study actually exists.
Can vaccine DNA contamination cause cancer or autoimmune disease? A meeting participant responded, “when you consider that almost every one of these vaccines is injected right into the tissue… I think you couldn’t do much more to get the DNA expressed [to get contaminating DNA taken up by human cells] than to inject it into a muscle in the way it’s being done.”
Again CBER’s Dr. Rebecca Sheets: “I think that the vast majority of licensed vaccines, US licensed vaccines, have not been tested for residual DNA.”
A more frightening question was raised as to whether it was known if there has been any presence of foamy virus. Foamy virus (HFV in human form and its more widespread parent SFV from monkeys), although not infectious, is a deadly carcinogen. To the participants’ knowledge, they did not know whether any laboratory has ever searched for it in vaccine preparations.
The meeting confirmed that a particular cell, “which under many conditions is neoplastic [tumor causing]” has been licensed for the production of both injectible and oral polio vaccines in the US, Thailand, Belgium and France. Therefore, these vaccines carry the high risk of containing cancer-causing oncogenes.
In order to appreciate the magnitude of the contamination problem in vaccine products, it is important to understand that vaccine filtration needs to allow the targeted virus’s passage to remain for vaccine use. Other particles and pathogens—DNA and RNA fragments from other organisms (and pathogens) in the manufacturing process, cellular substrates, and viral proteins--smaller than the vaccine’s virus will remain in the vaccine.
What the content of these meetings tells us is best expressed by one of the leading attendants at the meeting, Dr. Minor stated, “So even today then you have to bear in mind that a large amount of vaccine that’s made is made on really quite crude materials, from an adventitious agent point of view. It’s not a trivial usage. In fact, when considering what vaccines are actually made on these days, they are quite primitive in some respects.” Janine Roberts summarizes her investigations succinctly,
“In other words, the vaccines we give our children are liquids filled with a host of unknown particles, most of which came from the cells of non-humans: from chickens, monkeys and even from cancer cells. Truly we do not know what we are doing or what are the long-term consequences. All that is known for sure is that vaccines are a very cheap form of public medicine often provided by governments to assure the public that they really do care for the safety of our children.”
The conclusion that can be drawn from these meetings convened by our national and international health officials in vaccine science and safety is that vaccines are virtually genetic experiments, capability of causing mass cellular destruction, being injected into the world’s population, especially children. There remain so many unanswered questions about vaccine science. This includes the forthcoming swine flu vaccines that will include the contaminants mentioned above, if we take any of these meeting attendees’ words to heart.
If we are to express any awe and wonder it should be towards our body’s natural immune system and its ability to defend itself from the onslaught of vaccine brews. It is not vaccination that is a miracle of science, as the vaccine industrial complex, government health authorities and their congregations of believers are too eager to proclaim. In fact, the real miracle is the body’s ability to protect itself, in most cases, from the invasion of vaccines. Yet, even this statement is now turning suspect given the dramatic rise in multiple illnesses and inflammatory conditions across the age spectrum.
As with all living systems, whether it be a natural habitat in the wild, the planet’s climate system to support life, or the body’s immune system, a tipping point is eventually reached. Today, with the majority of the public still buying into the false promises of vaccination’s efficacy and safety, the vaccine industrial complex remains an extraordinarily lucrative business. More and more vaccines are now being developed for a wide variety of diseases and infections— Chlamydia, herpes simplex type 2, West Nile virus, Epstein-Barr virus, and others—that will only add to the overload of vaccines already recommended, especially to children who are officially recommended to receive 36 separate vaccinations by the time they reach 18 months of age. As these new genetic poisons are added to the national health agencies’ recommended vaccination schedule, a tipping point may be reached that will result in a more serious pandemic, a pandemic of Vaccine Disease, manifesting in myriad illnesses dependent upon each vaccinated person’s genetic predisposition and the robustness of the immune system, than any epidemic threat posed by wild infectious pathogens, including the H1N1 swine flu, that could unfold in our so-called developed, hygienic society.
Richard Gale is the Executive Producer of the Progressive Radio Network and a former Senior Research Analyst in the genomic industry. Dr. Gary Null is the host of the nation’s longest running public radio program on nutrition and natural health and a multi-award-winning director of progressive documentary films, including Vaccine Nation and Autism: Made in the USA.
Notes
(1) The following quotes and events were taken from Roberts, Janine. Fear of the Invisible: How Scared Should We Be of Viruses and Vaccines, HIV and AIDS Impact Investigative Media Productions: Bristol UK, 2009; and from an interview with Janine Roberts. The Gary Null Show. The Progressive Radio Network and WNYE-New York on August 19, 2009.
(2) “Serious Questions Regarding the Safety and Efficacy of the Influenza Vaccine” Vaccine Risk Awareness Network. http://vran.org/about-vaccines/specific-vaccines/influenza-vaccine-flu-shot/influenza-nursing-home-deaths/
(3) Ho, Mae-Wan, Cummins, Joe. “The vaccines are far more deadly than the swine flu”. Global Research. August 21, 2009. http://www.google.com/search?hl=en&source=hp&q=mae+wan+ho+global+research&aq=o&oq=&aqi=g10
Sourve: Global Research, September 29, 2009
Global Research Articles by Richard Gale
Global Research Articles by Gary Null…
Added by Anti Oligarch at 2:37pm on October 13, 2009
is research facility to seize a breakthrough cancer treatment called GcMAFMonday, July 27, 2015 by Mike Adams, the Health Ranger
<a href="http://ox-d.beforeitsnews.com/w/1.0/rc?cs=5125e7a33c8bf&cb=INSERT_RANDOM_NUMBER_HERE" ><img src="http://ox-d.beforeitsnews.com/w/1.0/ai?auid=326914&cs=5125e7a33c8bf&cb=INSERT_RANDOM_NUMBER_HERE" border="0" alt=""></a>
(NaturalNews) The history of the suppression of medical science in America is a long one, filled with true accounts of pioneering doctors and clinicians being threatened, intimidated and even assassinated in order to bury emerging cures and keep the “sick care” industry in control. (The American Medical Association, for example, has been found guilty by the U.S. federal courts of a conspiracy to destroy the chiropractic industry, by the way.)
Over the last few days, we’ve learned that before being found shot in the chest and floating in the river, pioneering medical researcher Dr. Bradstreet was working with a little-known molecule that occurs naturally in the human body. Called, “GcMAF”, this molecule has the potential to be a universal cancer cure for many people. It has also been shown to reverse signs of autism in the vast majority of patients receiving the treatment.
While GcMAF is perfectly legal as a treatment in dozens of advanced nations around the world, the U.S. Food and Drug Administration has outlawed it, calling it an “unapproved drug.” It is with this designation — an effort to suppress the forward progress of medical science — that the U.S. government conducted a raid on Dr. Bradstreet’s clinic, specifically seeking to confiscate GcMAF in order to shut down his research and halt his treatment of patients. Meanwhile, Big Pharma gets special permission to unleash untested, experimental drugs on the public as long as those drugs earn sufficient profits.
In this article, I summarize the videos, articles and documents covering GcMAF and the mysterious death of Dr. Bradstreet. An exhaustive investigation needs to be pursued on this matter, possibly involving private investigators. The timing and manner of Dr. Bradstreet’s death seems highly suspicious, especially in light of the many other holistic doctors who have recently been found dead under mysterious circumstances. (Dr. Nicholas Gonzalez died just days ago…)
Is there a motive for the murder of pioneering cancer researchers working on a possible universal cancer cure? Of course there is… it’s the most common motive in the world: MONEY 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. Key to their profitability is the inescapable fact that conventional cancer treatments simply don’t work most of the time, creating a reliable profit stream of repeat business from patients who are never cured (by design).
Would the cancer industry murder doctors to protect its profits? Of course it would. The industry kills patients as a routine part of its business operations! For example, an oncologist named Farid Fata was recently sentenced to 56 years in prison for falsely diagnosing patients with cancer so that he could sell them chemotherapy treatments they didn’t need. See the article Cancer doctors ‘fess up to making false diagnoses just to make more money.
Click here to search for “cancer false diagnosis” at GoodGopher.com, the search engine for truth seekers.
INVESTIGATION: Here’s what we know so farMultiple hat tips to all the outstanding citizen journalists, video creators and bloggers who have created the items cited below:
U.S. govt. search warrant document served against Dr. Jeffrey Bradstreet to confiscate GcMAF from his research facility.
Video that connects the dots between Dr. Bradstreet, GcMAF, cancer cures and the suppression of medical science by the U.S. government.
Video detailing the Dr. Bradstreet search warrant, served June 30, during which the U.S. government seized GcMAF from Dr. Bradstreet’s research clinic:
EzekielDiet.com story that covers the apparent series of murders of holistic doctors, many of whom are working on advanced treatment protocols that render high-profit sectors of conventional medicine OBSOLETE:Yet another doctor was just found murdered inside his home here on the East Coast of Florida. This makes six doctors to be found dead in the last month just from this region of the country alone. Four out of the six were found dead here in Florida. We lost the holistic Dr. Teresa Sievers, MD, who was found murdered in her Florida home just weeks ago. We’ve also lost the alternative Dr. Jeff Bradstreet, MD, who was found in a river with a gunshot to his chest. He’d recently moved to Georgia from Florida. We’ve also lost the Osteopath. Dr. Riley, who was found in Georgia at her home; just a few hours from the Florida border. She was found with a gunshot wound to her head. Now we’ve lost Dr. Schwartz MD, who was found murdered in his home, on Sunday, July 19th, 2015. This was four weeks to the day after the death of the first physician: (Dr. Bradstreet MD) who I broke the story on a month ago. His family is still seeking answers as to what happened to him and they’re some of the kindest people I know. The latest MD, Dr. Schwartz, in the picture above, lived just north of the fit, healthy, holistic Dr. Hedendal; who was the second doctor to be found dead this past Father’s Day, in Boca Raton. This was the same day that Dr. Holt died at the age of 33. Both were fathers; and again, both men died here in Florida on June 21st, 2015.
SCIENCE.NaturalNews.com entry describing the extraordinary benefits of GcMAF in a published study:
Stepwise incubation of purified Gc protein with immobilized beta-galactosidase and sialidase generated probably the most potent macrophage activating factor (termed GcMAF) ever discovered, which produces no adverse effect in humans…
After about 16-22 administrations (approximately 3.5-5 months) of GcMAF, these patients had insignificantly low serum enzyme levels equivalent to healthy control enzyme levels, ranging from 0.38 to 0.63 nmole/min/mg protein, indicating eradication of the tumors. This therapeutic procedure resulted in no recurrence for more than 4 years.
In other words, the administration of GcMAF eradicated tumors and left patients cancer-free for 4+ years with no additional treatment!
BOTH USA AND UK ‘GOVERNMENTS’ DESPERATELY SEIZING ALL SUPPLY, SHUTTING DOWN CLINICS, EVEN AS MILLIONS DIE FROM CANCER EVERY DECADE….
UK govt. admission that GcMAF was on track to being commercialized as a pioneering cancer treatment, so they had to confiscate it!
GcMAF (Globulin component Macrophage Activating Factor), a blood product, claims to treat a range of conditions including cancer, HIV and autism…
More than 10,000 vials were seized at this site and production of this unlicensed medicine has now ceased. These products were sold through various European websites and UK patients may have bought it from one of these websites. We are working with colleagues in other countries to alert them to the potential risks. Our investigations are ongoing and we have received no reports to date of side effects caused by this product.
That same page lists some of the websites where GcMAF had been available for purchase:
www.GcMAF.eu www.immunobiotech.eu www.immunocentre.eu www.petgcmaf.com www.firstimmune.fr www.firstimmune.de www.firstimmune.it www.gcmaf.gr www.gcmaf.se www.gcmaf.es www.gcmaf.ru www.gcmaf.pl
GcMAF is readily available as a medical treatment in Japan. This site explains:
GcMAF (Gc Protein derived Macrophage Activating Factor) – Gc MAF treatment is a highly effective macrophage activating therapy, used to stimulate the immune system and activate macrophages so that they can destroy cancer cells and other abnormal cells in the body.
From the FAQ page of the treatment clinic:
What exactly is Second Generation GcMAF? High Dose Second Generation Gc-MAF is produced using our new Patent Pending process which was developed here in Japan by Saisei Mirai in collaboration with Dr Hitoshi Hori and Dr Yoshihiro Uto at the University of Tokushima who have been studying GcMAF for over 20 years. Studies on GcMAF began at the University of Tokushima in 1992, after they were introduced to Dr Nobuto Yamamoto’s work and a collaboration began…
Second Generation GcMAF is made using a new and improved 2nd generation method of Gc-MAF production which is 10-20 times more concentrated and is more active and stable than other GcMAF that is currently available. Importantly, this much higher concentration GcMAF has been clinically demonstrated to be largely free of any side effects in the great majority of patients and is much more stable because it is resistant to oxidation.
That same site describes Oral GcMAF as follows: “Oral GcMAF is a form of GcMAF produced from bovine colostrum by Saisei Mirai which was developed in collaboration with Tokushima University.”
It also lists the following health conditions as being treatable with GcMAF, potentially a “universal cancer cure” substance:
Gc-MAF and/or oral Colostrum MAF macrophage activation therapy is indicated in the treatment of any diseases where there is immune dysfunction or where the immune system is compromised, such as:
Cancer Autoimmune diseases Epstein-Barr Virus (EBV) Hepatitis B virus (HBV) Herpes Simplex virus (HSV) Cystitis Hepatitis C virus (HCV) Multiple sclerosis (MS) Urinary tract infection (UTI) Autism Spectrum Disorders (ASD) Rheumatoid arthritis (RA) Endometriosis Chronic Fatigue Syndrome (CFS) Lyme disease (Lyme borreliosis) IgA deficiency disorder Myalgic Encephalomyelitis (ME) Mycobacteria infections Parkinson’s disease Tuberculosis Fibromyalgia Human papillomavirus (HPV) Lupus (Systemic lupus erythematosus, SLE) HIV AIDS Dengue fever Pneumonia infection Warts caused by viral infection Norovirus Malaria Influenza virus (flu) Herpes simplex virus (HSV) Q fever (Coxiella burnetii) Polycystic ovary syndrome (PCOS) Chicken pox (varicella zoster virus) Psoriasis Respiratory tract infections Ulcerative colitis, Crohn’s disease Type 1 diabetes (T1DM), insulin-dependent diabetes (IDDM) Type 1.5 diabetes, Latent autoimmune diabetes of adults (LADA)
Do you see yet why the medical establishment must SUPPRESS GcMAF and destroy all knowledge of its clinical applications? This one substance holds the potential to render numerous vaccines and pharmaceuticals utterly obsolete.
GcMAF protein described at NaturalHealth365.com:
Researchers and practitioners have demonstrated that GcMAF can reverse diseases that attack the immune system such as: chronic inflammation, bacterial and viral infections, chronic herpes, chronic acne, Lyme disease, fibromyalgia osteoporosis, Hodgkin’s, Lupus, MS, Parkinson’s and remarkably – autism.
A clinical study out of Italy on 94 children with autism showed that 83 of them made considerable progress while on GcMAF. The most common reported improvements involve:
• Cognitive abilities including attention and focus, learning and understanding, receptiveness and awareness of the environment and both receptive and expressive language gains.
• Social Skills including willingness to interact and communicate with peers.
• Behavior including less hyperactivity, less stereotypical behaviors and improved cooperation and compliance.
In another study of 1500 children with autism, 85% had high levels of viruses and a compromised immune system. All 1500 received weekly GcMAF injections and 70% of the children responded to the treatment with reduced symptoms and another 15% made full recoveries. The other 15% did not respond.
It was stated that the reduction of autistic symptoms is permanent provided that GcMAF has been taken long enough for the body to produce its own GcMAF which typically takes 24 weeks.
THE SYSTEMATIC SUPPRESSION OF MEDICAL SCIENCE TO PROTECT THE LUCRATIVE CANCER TREATMENT INDUSTRY (chemotherapy, oncology, radiotherapy, etc.)ANH-EUROPE.org covers the systematic suppression of advanced cancer treatments and cures:
Back in 1993, Nobuto Yamamoto, then working at Temple University School of Medicine in Philadelphia, PA, USA, first described a remarkable molecule. His paper reported the conversion of vitamin D3 binding protein (DBP, known in humans as Gc) into a potent macrophage-activating factor (MAF), known as Gc-MAF. Macrophages are a key part of the human immune system with two roles: to engulf and destroy pathogens and cellular debris, and to recruit other immune cells to respond to the pathogen.
Gc-MAF hasn’t had the benefit of a single patent owner – as a natural molecule, it cannot be patented without being modified – with the will and resources to push it under the noses of the public and health authorities. Dr Yamamoto has run small human trials in breast, prostate and colorectal cancers, with promising results.
David Noakes might just be the person to bring Gc-MAF into the mainstream. He’s the CEO of Immuno Biotech Ltd. and spokesperson for First Immune Gc-MAF, a project he describes as, “PhD and BSc biochemists and biomedical scientists… with external doctors, oncologists and scientists who kindly provide advice, committed to bringing some of the increasing number of published but relatively unused medical cures to as many people as we can.” At the moment, Noakes and his colleagues are supplying Gc-MAF to 30 countries where it is legal, via a network of “around 300″ doctors. Their Gc-MAF is made to extremely high standards, and is being used in ongoing clinical research by Noakes’ collaborators and others. Their ultimate goal is to, “Build the case that GcMAF is effective for various illnesses, which will help to make it available to the public”. GcMAF suppliers fighting for survival against a global medical monopoly that profits from disease
MUST-SEE website: http://gcmaf.se/
From the site:
The medical laws have been changed over the last 40 years so that all the brilliant breakthroughs in cancer are denied to the British public. Lord Maurice Saatchi had to watch his wife die, while his doctor told him the only thing he was allowed to prescribe her was chemotherapy, which would shorten her life. He hopes to bring the Medical Innovation Bill to Parliament, so instead of obeying a destructive government law, a doctor will be able to prescribe whatever treatment is best for the patient…
Bad law kills, and Britain has the worst medical laws in Europe. The 1939 Cancer Act makes it illegal to discuss the possibility cancer can be cured, which is partly why 160,000 people die unnecessarily of cancer in Britain every year. Science and treatments are decades ahead of where the medical industry is today. The MHRA’s job is to get life saving treatments like GcMAF out to people as quickly as possible. Instead they block them to protect billion dollar Big Pharma monopolies, who also fund the MHRA. Over a hundred thousand lives could be saved every year if the 1939 Cancer Act were repealed, and the MHRA were closed down.
There are 142 eminent scientists who have published GcMAF research papers on the US National Library of Medicine alone.
From the how GcMAF works page:
Your GcMAF empowers your body to cure itself. In a healthy person your own GcMAF has 11 actions discovered so far, including two on cells, three excellent effects on the brain, and 6 on cancer. Amongst these it acts as a “director” of your immune system. But viruses and malignant cells like cancer send out an enzyme called Nagalase that prevents production of your GcMAF: that stops its 11 beneficial effects, and neutralises your immune system. So diseases become chronic, and cancer cells grow unchecked.
Minutes after a receiving a dose, 10 of the body’s actions restart. In three weeks of two GcMAF 0.25ml doses a week, your immune system is rebuilt to above normal strength. You need two doses a week for typically 24 weeks for many diseases and early cancers, up to seven one ml doses a week and a year for stage 4 cancers. Your body then takes the disease down without side effects, and successfully in 80% of cases -depending upon how well you follow the protocol under “Treatment Protocol” on this website.
What is GcMAF? It is a human protein. One week’s GcMAF looks like a small raindrop. If properly produced it is perfectly sterile, and a most ethical course for doctors.
GcMAF is therefore a replacement therapy for those who can’t make their own. Taking GcMAF replaces the missing part of the immune system, and also acts as the body’s own internal medicine.
GcMAF is extracted and isolated; its a 24 step process, and at the end it must have tests to prove its sterility and activity. (If it does not come with published tests, its probably not GcMAF.) One GcMAF has been tested in universities, laboratories and clinics, where, as a result of the testing, consistent activity and sterility have always been found, and been the subject of 40 scientific research papers.
What does GcMAF do? The GcMAF Conference 2013 showed GcMAF is a far more powerful molecule than thought, both in terms of the science, and doctors’ results. In stage 4 cancer, some doctors who use the full protocol, listed on “Treatment Strategies,” are saving every patient (if they have not had chemotherapy.) Success can be achieved with all tumour cancers including breast, lung, prostate, pancreatic and melanoma.
GcMAF can eradicate chronic inflammation and viral infections. It is better than antibiotics in many areas, and 25% successful with Autism, 50% or more with Chronic Herpes, Chronic Acne, Chronic cirrhosis of the liver, Chronic kidney disease, Chronic depression, Colitis, Crohn’s, Fibromyalgia, Hepatitis, Herpes, LMBBS, ME/CFS, Osteoporosis, Periodontal disease, Psoriasis and various types of Immune dysfunction including allergies. Research shows GcMAF can halt deterioration in Parkinsons, multiple sclerosis (MS), dementia and ALS, and in its role of immune system regulator, can reverse diseases that attack the immune system like Lupus and Arthritis. And is effective with wound healing. Its successful with tumour cancers, and some others.
In addition to rebuilding a depressed immune system, GcMAF: Inhibits angiogenesis – stops blood supply to tumours Activates macrophages – phagocytosis and destruction of cancer cells Apoptosis – suicide of cancer cells Reverts the cancer cell phenotype to normal (Turns cancer cells into healthy cells) Reduces the metastatic potential of human cancer cells in culture. Increases energy production at the mitochondrial level – ME/CFS Improves human neuronal metabolic activity through cAMP signaling – autism, ME/CFS, MS, ALS Counters toxic effects including cadmium – ME/CFS
It abolishes neuropathic pain due to neuro-oxidative stress (stress due to the anti-cancer drug oxaliplatin) in the lab. (neurodegenerative diseases and autism that have oxidative stress as a pathogenetic mechanism) It increases neuronal connectivity by promoting differentiation and the formation of dendrites and neuritis (autism and ME/CFS, where there is a lack of connectivity between neurons).
See the 31 research papers published, particularly Brescia, and the 60 published by others listed under “The science”.
80% of terminal stage four tumour cancers cases can be saved (40% if they’ve had chemo), but usually when they are closely monitored, which is why residential Treatment Centres are being run in Switzerland. If they have three months to live and have not had chemo, almost no one needs to be lost.
The 180 scientists who have published papers on trials of GcMAF selected those in the early stages of cancer and HIV, and reported nearly 100 percent success, with no recurrence after many years. They did not attempt trials on people with large tumours.
Our trials are quite different: many people are over 50, some over 80, with advanced or terminal cancers, with significant tumour mass. Most come to us when their doctors tell them they can do no more.
The life of GcMAF is only six days – you have to keep taking it until your disease has gone (ie your nagalase is under 0.65 nmol/min/mg) then a further 8 weeks, or the immune system gets shut down again.
How long should you take GcMAF for? 8 weeks for chronic herpes/acne, fibromyalgia, inflammation. Allow 24 weeks plus of GcMAF for: Autism (85% improve, 25% eradication), CFS (70% eradication), HIV, Lyme (8% respond, most appear to have the VDR gene blocked and the viruses conceal themselves with biofilms) and stage 1 to 2 cancer, (80% respond). Late stage cancer, if you follow “Treatment Protocol” again has 80% responders, but it takes a year to 18 months to become cancer free. Cirrhosis of the liver: 16 months
Remember everyone responds differently. We can’t say how you will respond.
The more minor the disease, the easier it is for GcMAF to eradicate. GcMAF needs normal levels of vitamin D to function strongly (take 10,000iu a day). in low responders, larger doses are required.
We have probably proved GcMAF can work for people up to age 90, and can destroy large tumour mass. See “Participants experiences”.
If you have your blood taken for monocyte counts, relevant markers and vitamin D levels, and again for a nagalase test at the beginning, you should see on your next test after three weeks that your immune system is back to full strength, and after 8 weeks significantly falling nagalase will indicate the disease is losing its grip. Don’t stop the GcMAF until your nagalase gets below 0.65 nmol/min/mg, when it loses the ability to prevent your body producing your own GcMAF, and then you no longer need ours. Even better, get scans.
Autism children can improve at five weeks with substantial improvements at 8 weeks. See “Participants experiences.” But everyone is different.
The beauty of using your own immune system to attack disease or cancer is that it remembers how to defeat it for the rest of your life: it doesn’t come back. And unlike chemotherapy, the side effects are trivial.
The only way you can tell if GcMAF is genuine and active is to test with living cells in a laboratory. See “Quality and Tests of our GcMAF.” To recap:
We put live macrophages cells and MCF7 breast cancer cells together; nothing happens. Then we add GcMAF; in 72 hours the macrophages eat all the MCF7 cancer cells. We then put only GcMAF and MCF7 together, and the GcMAF turns the cancer cells back into healthy cells.
We have GcMAF available for preclinical trials. See “Buy GcMAF”.
You must read at least all of “Buy GcMAF” and “Treatment strategies” on the left if you want to take this further. And you must be prepared to give us feedback. Patent document on GcMAFSee the Yamamoto patent involving GcMAF:
Cancerous cells and HIV-infected cells secrete -N-acetylgalactosaminidase into the blood stream, resulting in deglycosylation of serum Gc protein. This inactivates the MAF precursor activity of Gc protein, leading to immunosuppression… When peripheral blood monocytes/macrophages of 175 cancer patients bearing various types of cancer were treated in vitro with 100 pg GcMAF/ml, monocytes/macrophages (phagocytes) of all cancer patients were activated for phagocytic and superoxide generating capacity. This observation indicates that patient phagocytes are capable of being activated…
Also see BetterHealthGuy.com coverage on GcMAF:
first heard about GcMAF almost a year ago. At the same time, I had first learned about “nagalase”, a blood test that is used to in part determine whether or not one might be a candidate for GcMAF therapy. Nagalase is an enzyme that prevents Vitamin D receptors (VDR) from being activated on the surface of the macrophage. As a result, macrophages are not “activated” and our immune systems are not able to properly respond to invaders.
Here are some points that I have learned thus far on GcMAF:
- GcMAF has reportedly been tested more for safety, purity, etc. than other human blood products. - Macrophages are cultured, destroyed, and the GcMAF receptors are purified. - Treatment is via injection 1x/week for 8-20 weeks. Dose is titrated initially to avoid exacerbation or Herx responses as much as possible. - A commonly used dose is .25ml once weekly (a 2.2 ml vial should last 8 injections). - The primary test used in looking at whether or not GcMAF may be a reasonable intervention is nagalase. - Nagalase inactivates macrophages. - I personally would NEVER consider this option without having a baseline nagalase test. Normal is < 0.95. Mine was 2.9.
The practitioner I worked with suggested that 2.9 was in the range of someone with HIV or cancer in terms of the impact on the immune system. I’d like to hear from others in the Lyme community as you get test results as well to see if there is a pattern of elevated nagalase in those with Lyme disease. Whether or not Lyme itself has anything to do with nagalase elevation is something I have not been able to find anything on. We certainly all have underlying viral co-factors that are likely in play as well, but I suspect that Borrelia may also play a role in nagalase elevation.
- In healthy college students, a nagalase 0.4 is not uncommon (the lower the better).
- At 2.9, my practitioner was surprised that I did not have more cognitive deficits such as memory loss and other cognitive issues.
- It has been suggested that ongoing antimicrobial therapy without a working immune system is like leaving the house with the door wide open inviting burglars in. By using GcMAF to activate macrophages, nagalase drops, and one may regain a functional immune system. The door is then closed to further invaders and we may no longer serve as a microbe hotel.
- Maintenance therapy should not be needed once the immune system is once again properly functioning.
- Activated macrophages only remain active for 7 days so any negative responses are generally short-lived. That said, some people do have strong inflammatory responses that are not believed to be typical die-off reactions.
- It has been indicated that in some cases, other medications may be needed in order to manage the inflammatory response. This is another reason that one needs to be working closely with a knowledgeable practitioner before considering GcMAF in my opinion. In the CFS and GcMAF world, this more severe form of a die-off reaction is called IRIS.
- VDR genetics do not seem to play a role in predicting response as earlier thought according to one practitioner that I have spoken with. That said, Vitamin D levels do correlate with the positive response rate of GcMAF. Thus, Vitamin D supplementation may be required in order to optimize outcome.
- Other than die-off reactions or activation of symptoms (inflammation), no other side effects are generally expected.
- Nagalase should be monitored every 1-2 months while on treatment to determine the required duration of the therapy. Target nagalase after treatment would be 0.4 to 0.6.
- Elevated nagalase has a profound detrimental effect on the immune system. Elevated nagalase is often presumed to be related to microbes of viral origin or cancer. Viruses that are nagalase producers open the door to chronic infections.
- Hemagglutinin contains nagalase and is also found in flagella of some bacteria so it could also be the case that some bacteria may produce nagalase.
- Parents with ASD children also often have elevated nagalase.
- A practitioner I spoke with likened Lyme disease to a “peat moss fire” burning below the surface. Activating macrophages should help to deal with the fire.
- GcMAF should be helpful in dealing with other infections that are not of viral origin; for example, Borrelia, Bartonella, and other infections commonly associated with Tick-Borne Infections (TBIs). GcMAF is active against many cancers and many different kinds of microbes.
- Neopterin is another test that is sometimes used as an indicator of immune suppression. As macrophages become activated, neopterin may rise and later fall. If one is in the normal range for neopterin and has an immune-related illness, this could be an indication that the immune system is suppressed and not responding appropriately.
- People with autoimmune conditions can generally use GcMAF. However, GcMAF may be contraindicated in people with Multiple Sclerosis.
- Reduction in nagalase is generally seen early in the course of treatment; within the first 3-6 weeks. In some studies, nagalase dropped by over 50% in less than six weeks.
- Cancer patients may initially feel as bad on GcMAF as they do on chemotherapy, but often feel much better after the first month.
- Anti-inflammatories may limited the effect of GcMAF.
- Enzymes and biofilm-reducing supplements may have a negative impact on GcMAF therapy and may be best avoided. It is still too early to know what the impact may be, but one practitioner I spoke with feels that it is best to avoid these.
- One should not be on any immune-suppressing agents while on GcMAF as the immune system must be partially functional in order to respond appropriately to the treatment.
- A common pattern is to see elevated lymphocytes, high nagalase, and low NK cells. Once nagalase drops, it may be the case that NK cell function could be positively impacted. CD57 is a type of NK cell. It is too early to know if this proves to be true, but it is one of the things I’m quite interested in.
Watch this video presentation on GcMAF therapy to learn more.
Read about GcMAF from Alternative-Health-Group.org.
Read The GcMAF Book at this link.
Open the “Stop Fighting Cancer” PDF document and search it for “GcMAF” to read some intriguing passages:
Researchers testing GcMAF stated it, “works 100% of the time to eradicate cancer completely, and cancer does not recur even years later.” (This was stated based on the tested group of patients -nothing works 100% for everyone) The weekly injection GcMAF, a harmless glyco-protein activates the human immune system which then can kill the growing cancer. Studies among breast cancer and colon cancer patients produced complete remissions lasting 4 and 7 years respectively. This glyco-protein ‘cure’ is totally without side effect but currently goes unused and completely ignored by cancer doctors. Why? Maybe it is because there is little money to be made in selling it. For less than $2000USD a cancer patient can obtain an adequate amount of GcMAC.
See the National Library of Medicine page Immunotherapy for Prostate Cancer with Gc Protein-Derived Macrophage-Activating Factor, GcMAF:
When human macrophages were treated in vitro with 100 pg GcMAF/ml for 3 hours and a prostate cancer cell line LNCaP was added with an effector/target ratio of 1.5, approximately 51% and 82% of LNCaP cells were killed by 4 and 18 hours of incubation, respectively [14,15]. This in vitro tumoricidal capacity of macrophages activated by GcMAF led us to investigate the therapeutic efficacy of GcMAF for prostate cancer. GcMAF therapy as a single remedy modality can eradicate metastatic breast and colorectal cancers most effectively…
Click here to search for “GcMAF” on GoodGopher.com, the new search engine for truth seekers.
Read this article from The Telegraph on how scientists are being assassinated because of what they know.
Learn more: http://www.naturalnews.com/050553_Dr_Bradstreet_GcMAF_cancer_therapy.html#ixzz3h8gtv92E
More news on Dr. Bradstreet
Learn these simple tips for preventing cancer naturally
Monsanto: The world’s poster child for corporate manipulation and deceit
Extreme bias at Wikipedia on homeopathic medicine
Guatemalan STD medical experiments were just one crime in a long history of medical-government collusion to use humans as guinea pigs
Vicious vaccine culture war now being waged against informed, intelligent Americans who seek to protect their children from deadly side effects
131 Ways for an Infant to Die: Vaccines and Sudden Death
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http://www.naturalnews.com/050553_Dr_Bradstreet_GcMAF_cancer_therapy.html
NESARA- Restore America – Galactic News
Source: http://nesaranews.blogspot.com/2015/07/breakthrough-cancer-treatment-called.html…
laces copper in the blood and tissue proteins, accumulating in multiple locations of the body, causing destruction, accelerating aging & death. All symptoms, disease & conditions are indications of iron poisoning & bio-available copper deficiency in the iron poisoned population.
Symptoms, disease and conditions correlate to the locations of greater proportions of iron deposits and the effect on organs: CANCER, DEMENTIA, HEART/CARDIOVASCULAR DISEASE, DIABETES, LUNG DISEASE (C.O.P.D.), GASTRO-INTESTINAL DISEASE, BLOOD DISORDERS; to mention a few of the major problem areas. Bio-available copper must be replenished to mobilize iron out of the body, restore health and longevity, and repair the DNA damage.
January-2014: Death Rate - 15, Birth Rate - 7, population decreased by 1.6-1.7 million in 2013 (United States) The abomination that causes desolation (depopulation) spoken of through the prophet Daniel;
The number of the mounted troops is 200 million: Population Countdown
Blood Types & Disease, Symptoms, Conditions Indicate Iron Poisoning: Nearly 95% of the population, who have alkaline blood type A and O and the acidic blood type B, have iron poisoning and copper deficiency. Iron has accumulated due to iron, iron uptake facilitators and copper depleters that have been added to the food and water supply. ( USDA Food Supply Nutrient (1909-2005) Schedules) Blood type distribution correlates to iron poisoning prevalence in a population: types A, B & O over A, B & O plus AB (AB is not poisoned, 7.00 neutral pH.) Iron poisoned blood types are alkaline or acidic; dependent on the proportion and locations of iron deposits and the affects on organs & their functions. The majority of the population are alkaline blood type A & O and correlate to the most prevalent pH of 7.40 (now 7.54 +), acidic blood type B correlates to pH of about 6.8. In addition to iron are radiation and vaccine poisons. Radiation shakes or vibrates blood proteins, breaking off the loosely bound iron and accelerating iron deposition. Vaccines contain nano-particle size parasites, termed “viruses” that thrive and replicate in the presence of iron deposits, and adjuvant to deplete copper status. Genetically damaged (GMO foods) increase iron availability and decrease copper availability. These chemical, biological and radiation poisons work together to decrease lifespan and birth rate. The iron poisoned population had a lifespan 45 years less than the healthy segment; that gap has now widened to over 50 years. Current lifespan is estimated at 65-70 years for the poisoned population. Many are now dying in their 60s, 50s, 40s (and younger); because the baby boomers were the first to be implanted by parasites via mass vaccination. The population is undergoing the final stage of extermination. USDA Food Supply Nutrients Schedule Correlates To Population Reduction Schedule: Compare the Population Extermination, Death Statistics (1900-2009), and USDA Food Supply Nutrient (1909-2005) Schedules. There is an apparent correlation between nutrient additions, the increase of nutrients, decrease in births & birth rate, increasing death rate, increasing disease prevalence. Note that mercury is not specifically listed in the USDA Food Supply Nutrient schedules, but was added to the food/water supply and other sources in greater quantities starting in 1996.
Chemical, biological and radiological poisons work together to generate toxic malformations (proteins) and inflammation, and destroy the vascular system/blood supply, thereby shortening lifespan & killing the host. These poisons have altered and damaged the proteins/DNA of the blood, vascular system and other tissues of the body, with the damage, copper deficiency and iron poisoning passing down through the generations. Starting in 1996, the copper depletion rate was significantly increased and coincides with the onslaught of increased amounts of copper depleted GMO foods (genetically damaged foods),, wireless technology, increasing prevalence of diseases and debilitating symptoms/conditions, weakened immune system, decreasing birth rate, increasing death rate, accelerated aging, and decreasing lifespan.
Vaccines were designed to implant nanoparticle-size parasites, (termed “viruses” – mainly measles), and adjuvant to deplete liver copper. The parasites settle, thrive & replicate in the presence of iron deposits and copper deficiency, and accelerate the destruction process by increasing the synthesis rate of abnormal toxic proteins; the consequences being an increasingly damaged vascular system, defective blood supply, inflammation, secondary bacterial infections, lesions, degeneration, fibrosis, tumors, and CANCER. The purpose of depleting liver copper with vaccine adjuvant: When the body is invaded by pathogens/viruses, copper is mobilized from the liver in order to neutralize/destroy them. Bacteria and viruses transition from the dormant state (time of injection) to the active state of thriving and replicating as iron stores increase and copper status depletes. The measles vaccine pathogen has been found in diseased colons of patients -- iron is taken into the body via ingestion and the gastrointestinal tract, and thus is a location for a greater proportion of iron accumulation. Measles settles in the mucosal linings of tissues/organs and other locations of iron deposits; where loosely bound iron breaks from blood proteins and settles. The parasite (“virus”) implanted by the vaccines coupled with the iron deposits accelerates the synthesis rate of abnormal toxic proteins; the consequences being inflammation, secondary bacterial infections, lesions, degeneration, tumors and cancer. The synthesis rate of toxic proteins increases as copper status depletes and iron stores increase, overwhelming the immune system and inevitably causing the demise of the host. Note: The MMR Measles vaccine was initially forced on the population beginning with the baby boomers, those born between 1946 and 1964, and subsequent age groups.
Radiation destroys the body through electrical oscillations that shake or vibrate cells and organisms (particularly the blood)– that is breaking up proteins into nonviable fragments, accelerating iron deposition, resulting in a significantly increased copper requirement. This destruction is apparent in an increasingly defective blood supply & damaged vascular system. (Optimal levels of copper are vital for normal healthy protein synthesis -- for building and repairing proteins.) This in turn accelerates the growth of nanoparticle parasites and cell destruction. Bisphenol-A does chemically what radiation does; that is, it breaks apart the blood proteins into nonviable fragments. Ninety-three percent of Americans test positive for bisphenol-A. More accurately, it is 93.34 %. (About 6.66% of the real population numbers do not carry the poison in their blood.)
Blood pH, Blood Types & Population Reduction: Sufficient Copper Intake Maintains Neutral Blood pH of 7.00: Copper is essential in the formation of normal healthy proteins, that is, normal amino acid sequences, as it provides a balanced pH state for the blood and tissues, maintaining the proper concentration of hydrogen for forming the bonds in normal protein synthesis. A balanced pH of 7.00 is present in blood type AB, which is the only normal blood type. The average pH of the alkaline blood types (A/O) was set up to 7.54 in 2005/06 while the pH of the acidic blood type B was set up to about 6.8. Alkaline and acidic blood types are caused by iron, and are dependent on the locations and levels of iron deposits in the body: liver, spleen, brain, glands, bone marrow, kidneys, lungs, colon, heart, etc. As copper depletes, and blood pH deviates further from neutral 7.00 pH level, iron accumulation accelerates and lifespan decreases. According to documentation on metabolic alkalosis, mortality rates have been reported as 45% in patients with an arterial blood pH of 7.55 and 80% when the pH was greater than 7.65. Mortality rates increase in the acidic blood type as well, with significant increases as the pH approaches 6.8.
The desired MASS KILL RATE aka "population reduction" rate was set up by increasing the pH level of the alkaline blood types to 7.54, while decreasing the pH of the acidic blood type.
The Rhesus Factor (D-protein) is a probable malformed or variant protein, resulting from insufficient copper levels. Moreover, we were not created with blood incompatibilities that would harm us and our unborn children, as known to occur with an rH negative mother and rH positive fetus, and with blood transfusions. The blood type AB is balanced and therefore does not carry the malformed Rhesus Factor protein as found in the other blood types, thus, only AB negative blood is possible.
Current Blood Type/Group Distribution in the U.S.: The previous blood type distribution, disclosed in about 1960 was AB 4%, B 10%, A/O 86%. Now with the copper depletion rate accelerating, the blood type distribution may approximate as follows: *AB 6.66%, B 30%, A/O 63%. Blood type B prevalence has increased significantly from 1960 until now, and can be observed in diabetes prevalence, which has a high correlation with type B blood. Type AB is the healthy unpoisoned blood type and their numbers can be calculated as follows: * When the poisoned blood types reach 200,000,000 blood type AB will be 6.66 % of the population – 14.27 million. Currently, close to 200 million of the 214 million in the population have iron poisoned blood types of A/B/O. This is written to explain what is spoken through His servant John, "The number of the mounted troops was 200 million, I heard their number." “Calculate their number, for it is 6-6-6”, that is 6.66 % of the real population numbers of the U.S.
Blood Type B Prevalence Indicates World Population Closer to 4 Billion: Researching the world blood types distribution, it is apparent from the high prevalence of type B blood (from 1959), that most of the rest of the world, excluding the western nations, has been in the final extermination phase for decades now, and thus, their numbers have been negative population growth. (Prevalence of type B blood increases as the population decreases due to extermination.)
United States Population Closer to 200 Million (as spoken through His servant John)
Use the following time table to refer to the pH Management/Iron Poisoning schedule (national average): Year pH Avg Daily Iron(mg)* Benchmark pre – 1900 7.38-7.40 *** 1900-1976 7.40 12.5 – 17* starting in 1900 coronary heart disease has accounted for more deaths
than any other cause or group of causes of death in the United States
1976-1980 7.43 16.8 – 17.1 set up to 7.43 over five year period; increasing deaths & declining births;
major cardiovascular deaths start slow decline due to initial stage of population reduction
1980-1995 7.43-7.45** 17.0 – 22.6 steady increase of deaths; steady decrease of births; population numbers peaked ~1980-81
1996-2006 7.54 22.9 – 23.4 target pH set up by 2006; exploding disease prevalence; steady increase in deaths; steady decrease in births * Daily iron available on USDA web site from 1909 to 2006. The years 2007 to 2014 are not accessible. ** Average is estimated. *** Mass iron poisoning began about 200 years ago in the 1800s, evidenced by world population increasing exponentially in the 1800s. This was due to substantial increase in birth rate/decrease in gestational period. Lifespan and gestational period decrease due to iron poisoning.
The average blood pH in the late 1800’s ranged from 7.38-7.40 (19). Approximately during the turn of the 20th century in 1900, there appears to have been a blood pH increase, and may be when the pH was initially increased to 7.40. According to the American Heart Association, since 1900, "coronary heart disease has accounted for more deaths than any other cause or group of causes of death in the United States". About in 1980 the average alkaline blood pH was set up to 7.43, and is the marker for peak U.S. population numbers due to the initial stage of population reduction, (Population Reduction Chart). The set-up to critical 7.43 would have been initiated in about 1976. The 7.43 pH level is adjacent to 7.45, the next life critical level, and would explain the steady increase in total number of deaths and declining births beginning in 1980. (Note: the year 1980 marks the peak population for the national numbers. The final extermination phase was initiated in 1996 and set up by 2006 at the pH level of 7.54, adjacent to the next life-critical level of 7.55 pH. This final phase of extermination marked the beginning of exploding disease prevalence, and can be researched from national health statistics data. (Critical blood pH levels: "Metabolic Alkalosis" -- life critical pH levels)
The Population Reduction Chart data estimates a period of 26 years was used to set up the blood pH to 7.54; a gradual increase that would go undetected by the population.
By 2013, the annual population reduction rate was about .72%, with death rate of 14-15. The official population numbers conceal the real numbers, starting in 1980-81, by inflating births. Calculate the actual population numbers by decreasing 1% each year: 68% of the official 2013 numbers, 69% of 2012 numbers, etc.
The U.S. population peaked at about 230 million in 1980-81, and is close to 214 million in February 2014, a decrease of 7.0%. Death Rate: The reported total death numbers appear to be valid up until 2006, when the alkaline blood pH was set to 7.54. The official death numbers for 2006 and later are understated.
The death estimates for these years were calculated by using a state with an earlier extermination schedule as reference, by aligning the state and national schedules, and Census 2010 adjustments.
The death rate as of December 2013 was estimated at 14-15, not the estimated official rate of 7.8. The number of deaths by age group is fraudulent starting in about 2005; the older age group deaths peaked in 2003, and began phasing out in 2004.
The official CDC death numbers for these age groups continue to rise and as of 2013 are at/exceed 800,000 for the 85+ group. This is done to conceal the increase in deaths of the under-75 year age groups; and to make it appear lifespan is increasing.
Diabetes and Type B Blood Prevalence Increase as Population Decreases: Diabetes correlates to type B blood: Diabetes was chosen for the purpose of this writing because it correlates to blood type B, thereby making it easier to isolate the type B blood from the alkaline blood types in disease. The diabetic linked blood is the acidic of the blood types; and is known to have an elevated acidity level due to higher iron content.
(Diabetes is the only officially recognized disease linked to iron poisoning – “iron overload”.) According to documentation, diabetes is associated to a blood pH of approximately 6.8; the alkaline blood types A&O correspond with the vast majority of the population and a blood pH of 7.4 (currently7.54+). (TRUE diabetes correlates to type B blood; artificially "raised blood glucose levels" can be induced by medications.)
Diabetic Keto-Acidosis (DKA) occurs when the blood becomes dangerously high in acidity, and is treated with alkaline chemicals. Additionally, references indicate that about 20% of African Americans and 10% of Caucasians carry the type B blood in the US, which is why African Americans are at twice the risk of developing diabetes than Caucasians.
Dated documentation indicated two thirds of diabetes cases were diagnosed, and therefore comprised approximately two thirds of the type B blood prevalence when the population was still increasing. However, current reporting indicates diagnosed diabetes correlates to one third of type B blood prevalence; two thirds are undiagnosed -- termed “pre-diabetic”. This is due to a rapidly increasing death rate and decreasing birth rate. Diabetes prevalence increases with a corresponding increase in type B blood; due to the alkaline blood types of A/O dying off at a higher rate than blood type B. Type B blood appears to have increased from 10% in the 1959 to about 30% in 2013 based on the current diabetes and pre-diabetes prevalence of the population. The accelerated deaths of the alkaline blood types are followed closely by blood type B which is also at an accelerated death rate, all due to iron poisoning and fatal copper deficiency status.
Blood type AB is normal, healthy: Only the death rate of blood type AB is normal with a healthy average lifespan of 120 years. As of 2014, they live over 50 years longer than the poisoned population. They have concealed this by moving multiple times during their lifespan, changing name and date of birth when they move, changing place of birth, adoptions, spelling variations & order of names, multiple marriages, identity switching, changing their appearance, and falsifying documents/records. Because they age very slowly, they hide or blur their identity and whereabouts in the beginning decades of their lifespan. They age slowly because they do not have oxidative damage from iron poisoning.
Diabetes Prevalence Graph, Interpretation & Analysis Comments: In 1996 a steady significant increase started in the 45-64 yrs age group, concurrently with 65+ yrs age groups. Prevalence of Diagnosed Diabetes by Age, United States, 1980-2009. The graph is misleading in that the institutionalized population is no longer included in the graph as of 2006*, when the final blood pH/extermination phase was set up for the general population. So, assume diabetes prevalence is significantly higher at least in the 65+ age groups in the years 2006 and later, as they would comprise a sizeable portion of the institutionalized population. Even without the institutionalized population, the graph clearly indicates that diabetes prevalence is much greater in the top tier age groups indicating that type B blood has a greater prevalence in these age groups than in the overall population. This does not mean that individuals with the alkaline blood types A and O are changing over to the acidic blood type B, but that many with the alkaline blood types are now dying in their 40s, 50s, and 60’s. Although a shortened lifespan, individuals with type B blood have a longer life expectancy on average, than the alkaline blood types. Note that Alzheimer's, kidney disease, liver disease, heart disease, strokes, and amputations are all linked to diabetes, all of which greatly affect quality of life. Lastly, the decreasing lifespan in the alkaline blood types will cause a corresponding increase in the percentage of individuals with type B blood in the overall population, as well as an increase in the percentage of individuals with type AB blood. (*In October 2008 when CDC added in the year 2006 to the graph, a notice appeared on the web site indicating the institutionalized population is not included.)
The year 1996 is when the copper depletion rate increased, indicated by increases in diabetes and other disease prevalence, in addition to reduced birth numbers. The year 1996 coincides with the onslaught of GMO - High Fructose Corn Syrup which is known to contain mercury, a powerful poison that obliterates copper stores. Mercury is also known to reduce birth numbers, spontaneous abortions, stillbirths, congenital malformations, infertility, and inhibition of ovulation.
The American Diabetes Association reported in 2011, an estimated 30% Americans had pre-diabetes or have been diagnosed with diabetes. This may indicate the percentage of type B blood in the overall population has risen from 10% in 1959 to approximately 30%, with much of the increase occurring from 1996 to present. Also, according to the source, American Indian, African American and Hispanic/Latino have an increased risk of developing diabetes. This is because these groups started out with a greater degree of copper deficiency & iron poisoning and thus, a greater percentage of type B blood than Caucasians. -- Note this is why these groups had a higher death rate and/or shorter lifespan than Caucasians. However, Caucasians have now caught up to the other groups, starting in 2006, when the pH level of the alkaline blood types reached 7.54, thus accelerating iron accumulation. (see: pH chart) Of all the groups in the U.S., American Indians appear to be the most decimated, as evidenced by the high rate of diabetes and short lifespan among some tribes, such as the Lakotah Nation. <!--[if !supportLineBreakNewLine]--> <!--[endif]-->
Evidence of Lower Than Reported Birth Numbers: According to reports released in February 2007 and April 2009 , fetal deaths number about 1 million per year in the United States. The number of fetal and infant deaths to the number of actual births plus fetal deaths, reveal 40% of children die within the womb or outside the womb within a year after birth. This is strong evidence that births are in decline; the official birth numbers are inflated to conceal this. National sources report fetal deaths of 20 weeks or more of gestation which account for only about 25,000 of the 1 million fetal deaths. Birth estimates by year can be found here: This chart approximates the population reduction schedule and estimates birth numbers based on death numbers and yearly population decreases. Decreasing Gestational Age at Birth: Gestational age has decreased significantly between 1990 and 2005, Births By Gestational Age in the United States. A significant decrease is indicated from 40+ weeks and a significant increase is seen in the 37-39 weeks of gestation. The gestational period is decreasing due to increased amounts of iron and an increasingly severe copper deficiency being passed on to the fetus. A shorter gestational life does NOT indicate a normal healthy birth rate, and is an additional indicator that births are decreasing. A normal healthy gestational period in humans without iron poisoning and copper deficiency is estimated to be about 52 weeks -- one year. (Note that reported gestational period is calculated based on "first day of Last Menstrual Period", so actual gestational period is 1 to 2 weeks less than reported.) The healthy blood type AB has the longest gestational period, therefore the lowest birth rate, when the rest of the population is still increasing.
Age Distribution: The inflated birth numbers obfuscate birth decline, decreasing lifespan, increasing death rate, negative population growth. The low birth numbers shift the age distribution by decreasing the percentage of the lower age groups. As of 2014, approximately 12.5 % are <15 years of age; while the 65+ year age groups comprise about 12% of the real population numbers. In 1980 the <15 year age group was 24% which was twice the 65+ year group of about 11 % of the population. Now, in 2014, the <15 year and 65+ year age groups are approximately equal. When there are as many elderly people living as there are young people, it creates the illusion that a population is living longer, when in fact lifespan is decreasing. Note, just as gestational life decreases, so does lifespan outside the womb. Additionally, disease prevalence indicates a significant and steady increase, particularly since 1996, when the copper depletion rate was accelerated. Exploding disease prevalence is not indicative of a healthier longer living population, but of a population going into extinction – methodical extermination. The manipulated age distribution and inflated birth and population numbers are masking the true status of the health of the nation. The U.S. Government implemented the Immigration Act of 1996, coinciding with the year of accelerated copper depletion, and ahead of anticipated greater birth declines caused by the increase of mercury and iron. A primary intent of this legislation apparently is to prop up student enrollment numbers using external populations to obfuscate the true numbers. Although, these populations are not counted as the total number of the resident population, their numbers are used to artificially inflate the under-18 year age groups. Additionally, apparently to fill in where "enrollment has declined", three and four year olds are now attending school and are counted in total enrollment. <!--[if !supportLineBreakNewLine]--> <!--[endif]-->
Historical World Population Growth Rate Correlates to Initiation of Mass Poisoning: World population increased exponentially starting in the 1500's, and is a good indicator of the birth rate increasing significantly due to a decrease in gestational period. Thus, it was about in the 1500's that mass iron poisoning began.
Decreasing Lifespan/Increasing Death Rate: The 85+ year age group numbers peaked in 2003 and began phasing out in 2004, and many are now dying in their 60s, 50s & 40s. The official numbers show the 85+ numbers increasing significantly starting in 2005, to conceal the phasing out of this age group and to make it appear lifespan is increasing. The lower age group deaths are now increasing significantly, although the official numbers show little change.
The illusion of increasing lifespan: As death rate increases, the 85+ age group deaths increase, thereby increasing the average age at death*; making it appear lifespan is increasing,
but only temporarily until phasing out significantly.
Death trends by age groups can be observed in the death statistics for Blacks and American Indians, who are further along in the extermination schedule, and may have reached the life-critical iron levels & copper status before the 1980's. This explains why American Indians and Blacks had historically a shorter average lifespan. All groups are now undergoing the final phase of extermination, with the average lifespan estimated (conservative) at 70 years, a decrease of 5 years in approximately 9-10 years time.
As mentioned previously, the lower age groups of particularly the 40-64 years have increased significantly in the current stage of extermination: Reporting by national sources in October 2008, Baby Boomer Deaths Could Fuel Funeral Industry, indicated that many of the baby boomers, born between the years 1946 - 1964, are scheduled for extermination in the decade, 2009 - 2018. (Note that MMR Measles vaccine parasite implantation began with this age group.) The article also indicates the overall average national death rate is expected to increase from 8.1 to 10.9. Since the report is using understated death rates, the actual death rate could be expected to reach well beyond 15. The death rate appears to have steadily increased since 1980 and as of December 2013, is estimated to be 15. -- data in this chart are estimations only. These are indicators that not only is the population not increasing in numbers as we have been led to believe, but is in fact decreasing. (Note: death rates, total death numbers, death numbers by age group for 2005 and later are fraudulent.) *The 45+ age group is used in calculating the average age at death due to chronic iron poisoning: to exclude infant deaths, most external causes of death that typically occur under the age of 45, and deaths due to acute virulent disease. (Note that official reported total death numbers & numbers by age group starting in 2005 are invalid -- fraudulent.) Death numbers for the 0-44 yr age groups are high in the first and mid part of the 20th century due to a much higher birth rate & infant mortality rate, and acute virulent disease; resulting in a much higher death rate for the overall population. Although inhalation and body fluids may account for some transmission, it is likely disease causing parasites (“viruses”) were propagated through the food and water supply. Just as the chemical poisons have been carefully managed, so have the biological poisons. Disease manifested in the population on a mass scale ahead of and in preparation for the vaccine fraud. Although infant deaths were much higher in earlier years, as of February 2007 reporting, the fetal deaths number about 1 million per year. Note that 2006 was the year the final phase of extermination was set-up.
Factors for deaths across a wide spectrum of age groups (excluding external causes): variable individual copper depletion and iron accumulation rate, immunizations, copper status of ancestors upon settlement in the U.S. traced to area and country of origin, and different population reduction (poisoning) schedules by area and state in the U.S.. The initial poisoning apparently started before colonization began (and "evolution theory" fraud evolved) and traces back to the country or area of origin.
The Global Warming/Climate Change Fraud: When copper deficient, the body attempts to counter the rising blood oxygen levels that iron attracts; by retention of carbon dioxide (CO2). It is not the Global Warming fraud, an increase of carbon dioxide in the environment that is causing humans to die off. The fraudulent global warming science or climate change science explains that the elevated CO2 level in blood is caused by increasing CO2 levels in the atmosphere/environment particularly in the last 50 years. This is used for evidence the carbon cycle is causing the alkaline blood types O and A to go into extinction first, followed by blood type B.
The last disclosure of blood type distribution was about 50 years ago, when the alkaline blood types were at a higher prevalence and the acidic blood type B was at a lower prevalence in populations. The upcoming disclosure of blood type distribution reveals decreasing blood types A/O prevalence and increasing type B prevalence will prove that CO2 levels are rising. (See above section on current blood type distribution in the United States.) In truth this is evidence populations are dying off, have been in negative population growth, with much of the world in the final extermination phase for decades now. The last remaining nations, the Western nations, were set up in the final extermination phase in 2006. Like the United States, these western nations populations peaked in about 1979-1980. (Nations populations may have peaked a few years earlier or a few years later than 1980-81, and is dependent on current death rate and type B blood prevalence.) The remaining blood type AB, the only normal healthy blood, will be the ones to survive; hence -- survival of the fittest. <!--[if !supportLineBreakNewLine]--> <!--[endif]-->
Blood Type History & Theory of Evolution Frauds: In 1900, it was noted that the sera of some individuals led to the discovery of ABO blood types. (1) Essentially, noted a distinct difference in viscosity/pH level or the clotting factors of blood. Later on the blood type AB was "discovered". Subsequently, in 1940, the “Rhesus Factor” (D-Protein) was detected. In truth, there is only one blood type among humans, and that is type AB. Anything else is a mutation due to copper deficiency and iron poisoning.
As each generation has been iron poisoned and deprived of copper, the mutated genes/proteins have become weaker. These mutations of the blood and other structures that have manifested over the generations, is used as supporting evidence for the fraudulent Evolution Theory. The mutated blood types of A, B, and O and the presence of the Rhesus Factor are used to establish a lineage/correlation of the vast majority of the human population to the man-apes. This correlation does not exist, since humans are created solely with blood type AB, and the man-apes do not carry this blood type.
Blood types and DNA are used to establish fraudulent migratory patterns of different populations around the world. The higher the percentage of type B blood in a given population correlates to a more severe copper deficiency in that population. This is because the type B blood has a longer lifespan on average than the alkaline blood types of A and O. In other words the alkaline blood types are dying off much more quickly than the blood type B, and in fact are in the process of moving toward extinction, followed closely by blood type B, all because of copper deficiency & iron poisoning. It should be mentioned here that according to (2), in 1959 20% of Black Americans had type B blood and Caucasians had 10% type B, different severity levels of copper deficiency & iron poisoning, indicating that Blacks were copper deficient & iron poisoned before being brought over on slave ships. (One last note is, there were a small number of populations that contain only alkaline blood types, but these populations may have been manipulated by intentional extraction of the type B blood to fit the fraudulent theory.)
We were all created with type AB blood, with normal viscosity/balanced pH level with normal protein structures. Through a misinformation campaign the official history is that blood type AB is the newest and rarest, emerging 500-1000 years ago, while blood type O is the oldest. It is interesting to note that the Shroud of Turin, the suspected burial cloth of Jesus, has blood type AB. The cloth has been dated to about the first century AD, and as of yet has not been disproved. The truth is, blood type AB has always existed. The other mutated blood types appeared on a mass scale about 500 years ago when the poisoning began. <!--[if !supportLineBreakNewLine]--> <!--[endif]-->
Vaccination Fraud: vaccines were developed under the cover (lie) they will protect from harmful viruses and bacteria, and were never needed and are another fraud perpetrated on the people. (Read "Principles of Vaccination" and learn how the fraud evolved.) Harmful viruses and bacteria thrive and replicate in the blood types A, B & O, which have blood pH that has deviated away from a neutral pH of 7.00. An unbalanced blood pH inhibits normal activation and function of the enzymes required to fight off harmful viruses and bacteria. Enzymes are made up of proteins and if any are missing or malformed due to copper deficiency, they do not activate and function at normal levels. A neutral blood pH of 7.00 destroys/removes (neutralizes) harmful bacteria and viruses because the enzymes activate and function at normal healthy levels due to sufficient levels of copper, providing proper concentration of hydrogen to form the protein bonds. Thus, the blood type AB is the normal healthy blood type with a neutral pH of 7.00 and has healthy immune function, and normal DNA. (Note: The blood types of A, B & O have plenty of iron; THE nutrient for ALL pathogens.)
Vaccination is in fact the most effective and efficient method to transport poisons more directly into the liver, to displace and deplete copper from that location. The liver is where many of the proteins are synthesized and is where the greatest percentage of copper is stored. Copper is vital in protein synthesis. Mercury, contained in most vaccines, settles and accumulates in the liver and obliterates this vital store of copper. Consequently, severe disruption/impairment of protein synthesis follows, resulting in increasingly severe DNA damage, and symptoms and conditions. <!--[if !supportLineBreakNewLine]--> <!--[endif]-->
COPPER INFORMATION
Copper Functions as the Primary Antioxidant: Copper maintains mineral balance, thus a balanced pH with normal blood viscosity, by functioning as the primary antioxidant in the body. (Copper mobilizes the oxidant IRON out of the body.) When the blood is of normal viscosity with optimal blood flow, the blood is able to rid the body of toxic metals -- iron, chemicals, and any overload of other minerals, (and harmful bacteria and viruses), thereby retaining and balancing out the nutrient minerals. It has been documented that a "decrease in antioxidant protection caused by copper deficiency goes beyond a decrease in the activity of copper-dependent enzymes by inducing a wide range of disturbances in the other enzyme systems. (4)" This is because copper provides a balanced neutral pH of 7.00 that is required by these enzyme systems in order to activate and function at normal levels. Enzymes are made up of proteins and if any are missing or malformed due to copper deficiency, they do not activate and function at normal levels. These other enzyme systems are involved in the formation of bone and connective tissue, immune system, cardiovascular and heart, brain, liver, blood vessels, pigmentation, collagen and elastin, blood clotting factors, all the glandular systems, and many others. (4) Thus, it can be stated with certainty that copper is the single most important nutrient in the body. This is why copper is the target for deprivation and depletion.
"The ability of copper to easily accept and donate electrons explains its important role in oxidation-reduction (redox) reactions and the scavenging of free radicals." (copper info site)
Restated, copper deficiency causes a complete breakdown of the blood's ability to eliminate iron from the body. Loosely bound iron breaks off from the blood proteins and accumulates in various locations of the body, which then acidify those locations causing serious life threatening disease states such as cancer, cardiovascular disease, diabetes, obesity, inflammation, immune deficiencies, neurological dysfunction, tissue and organ destruction, and many other diseases and symptoms, and an early death.
IRON INFORMATION
Iron is the PRIMARY poison: Iron accumulation coupled with parasites is particularly destructive and symptoms/conditions include but are not limited to: inflammation, Crohn's, colon and other cancers, diabetes, destruction of the pancreas, liver disease/destruction thereof, cirrhosis, heart failure/disease, destruction of the heart muscle, arrhythmias, palpitation, pulmonary diseases, anemias, fibrosis, skin pigmentation abnormalities, stomach, endocrine glands, adrenal insufficiency, physical weakness, "feminization" of males, and always -- an early death.
"Iron is essential for oxygen transport in the blood": Iron attracts oxygen, thereby causing free radicals, and facilitating the growth of parasites; subsequently stimulating the growth of tumors, cancers and bacteria.
"Iron Deficiency Anemia (IDA)": IDA is characterized as abnormal size/count of blood cells, accompanied by low blood iron levels. IDA is often described as being secondary to copper deficiency as well as to another concurrent disease or condition. Documentation also indicates that copper is needed to mobilize iron from deposit ("storage") sites into the blood. (This is where the copper deficiency comes in.) So, sub-optimal levels of copper will mobilize some iron from deposit locations into the blood; however, will not be enough to excrete the iron. If optimal healthy levels of copper are taken in and maintained in the diet, ALL the iron would be mobilized out of deposits, neutralized and excreted from the body. At the same time copper would replace the iron in the blood and tissue proteins, build normal blood cells to healthy levels, and neutralize the blood pH to 7.00.
The symptoms associated to IDA are indications of copper deficiency. Iron deposits in the bone marrow and liver interfere with protein synthesis – missing and malformed proteins are a sign of copper deficiency.
All the iron has been made bio-available, so there is no iron deficiency; the problem is iron metabolism because it is not required by the body. All pathogens do require iron to thrive and replicate; that is why diabetes, cancer and virtually ALL other disease prevalence is soaring. <!--[if !supportLineBreakNewLine]--> <!--[endif]-->
Women live longer on average than men due to some iron excretion: Males accumulate iron more rapidly than females due to the slightly more excretion of iron by females through menstruation and child bearing (Average: 25mg and 500mg, respectively). This explains why males have a shorter lifespan on average than females, and why females develop more severe symptoms after menopause. The total iron excretion due to menstruation and childbearing during a lifetime is estimated to be about 15 grams. Thus, men of the same age as postmenopausal women have on average five years less of lifespan due to an estimated additional 15 grams of iron accumulation. (Note that this is just a small fraction of the total lifetime accumulation of iron.)
Bound & Unbound Iron: When iron is in abundance and copper is deficient, iron is present as bound or unbound form. Loosely bound iron has taken the place of copper in the blood proteins and in accumulation of tissue & organs. The accumulation of iron in organs and tissues is referred to as hemosiderin, and is explained as “storage iron”. Strongly bound iron is found in abnormal toxic proteins such as bacteria, cancers & tumors; iron facilitates the growth of tissue and organ destroying proteins. Due to decreased levels of copper antioxidant activity, only extremely small amounts of bound/unbound iron can be mobilized from “storage” and blood, and subsequently neutralized/excreted from the body. Thus, iron CANNOT be removed from the body with concurrent copper deficiency. Copper must be replenished to replace the iron, retain & balance the NUTRIENT minerals, and restore health and longevity.
Destructive metals accumulate due to an unbalanced blood pH, severely diminished anti-oxidant protection caused by copper deficiency, and the intentional addition of iron and other toxic metals, and iron absorption facilitators, to the entire food and water supply. It appears the agenda was to deplete copper down to predetermined levels at specified periods in time. Subsequently, the final (accelerated) copper depletion schedule occurred from 1996 to 2006, resulting in an extremely severe, fatal level of copper deficiency. The current levels of copper obliterate the body's mechanism for healing, building, and repairing DNA damage -- that is normalizing body tissues, blood, organs, etc, to a healthy status. Now iron and other toxic metals are accumulating at an accelerated rate, thus expediting the extermination of the population.
Note: contrary to reports, alkalizing the blood and body will not cure the problem, and will only deplete more copper and move the pH further away from 7.00. The solution is neutralizing the pH (7.00) by balancing the nutrient minerals. The mineral that provides this function is copper. Thus, the solution is to replenish copper and remove copper depleting poisons and iron from the food and water supply, cease vaccines, and eliminate or isolate other man-made environmental poisons such as radiation. <!--[if !supportLineBreakNewLine]--> <!--[endif]-->
The Myth of Disease: (4,5) In their multitudes of scholarly medical works there is virtually always mention of missing and variant proteins in regards to different diseases. Parasites coupled with copper deficiency and iron poisoning cause variant malformed, missing, damaged DNA/proteins, and are responsible for virtually EVERY "disease" and symptom manifesting now, accelerating aging and death. Parkinson's, Alzheimer's, MS, mental depression, diabetes, autism, other neurological diseases, ADD, ADHD, pancreatic & digestive problems, inflammation, inflammatory diseases, obesity, bleeding disorders, anemia, low hormone production, levels of bad (malformed) hormones/proteins, bad (malformed) cholesterol, hypothyroidism, hyperthyroidism, hypo-adrenalism, hyper-adrenalism, cystic fibrosis, many other birth defects, congenital malformations, infant and fetal deaths, cancer, bone & muscle degenerative conditions, shortened lifespan, heart/cardiovascular disease, heart attack, stroke, allergies, respiratory illness, C.O.P.D., bronchitis, asthma, emphysema, kidney disease, liver disease, hearing and visual problems, and the list goes on. These things happen gradually over time, so we do not suspect we are slowly being poisoned. (10 for neurological diseases being caused by copper deficiency – brain destroying parasites.) <!--[if !supportLineBreakNewLine]--> <!--[endif]-->
"Man's days will be 120 years."
"Never again will an infant live but a few days."
Meanwhile, many people are dying and suffering needlessly, because they are copper deficient and iron poisoned. Amputations, disembowelments, open-heart surgery, radiation & chemo "therapies", and countless other unnecessary procedures and medications are being administered. Families, loved ones, and friends are dying and suffering all around us, and our ancestors were killed in the same manner.
"How long, Sovereign Lord, holy and true, until you judge the inhabitants of the earth and avenge our blood? ..They were told to wait a little longer, until the number of their fellow servants and brothers who were to be killed as they had been was completed.- - 200 million is reached"
Blood type is nothing more than the prevalence of iron poisoning & copper deficiency in the vast majority of the population. The blood type AB have survived through this, indicating that some areas of the world and/or some groups have been excluded from the poisons or have the remedy -- the poisoners themselves.
"Survival of the Fittest" = Survival of the Unpoisoned <!--[if !supportLineBreakNewLine]--> <!--[endif]-->
COPPER MISINFORMATION Copper toxicity caused by copper overload: The copper overload disease or "copper toxicity syndrome" is caused by copper deficiency. This phenomenon is characterized by the presence of bio-unavailable copper accompanied by a lack of circulating ceruloplasmin, a copper transport protein. Due to the bio-unavailability of much of the copper, the body cannot accomplish the tasks of building, repairing, and healing to normal levels, resulting in symptoms and disease states. This phenomenon further emphasizes the importance of copper's function in the body. However, based on the bio-unavailable copper, this phenomenon is routinely erroneously described as the presence of toxic levels of copper, when in fact it should be described as diminished levels of ceruloplasmin due to bio-available copper deficiency. Copper in its natural, untampered with, bio-available form is essentially non-toxic and any excess is readily excreted from the body.
Copper pennies, water pipes & bracelets replace copper: Man-made alloys such as copper pennies, water pipes & bracelets do not contain bio-available copper and therefore do NOT replenish copper. The idea of using copper water pipes/lines was concocted to provide a link or explanation for the "copper toxicity syndrome" fraud. This is apparent in fraudulent documentation that routinely mentions copper water pipes/lines in conjunction with "copper toxicity syndrome". Hair analysis shows copper toxicity: Hair analysis results have been used to erroneously identify "copper toxicity". Hair analysis reveals what is being excreted out of the body. The copper in hair analysis can show varying levels of copper output depending on an individual's release of copper (individual biological response to disease states) and the types and amounts of copper depleting poisons that are being taken into the body. Regardless of the copper level output in a hair analysis, a presence of mineral imbalance indicates copper deficiency. Sufficient copper levels are essential in neutralizing the blood pH, by removing iron and retaining and balancing the nutrient minerals.
"Copper Rich" foods are plentiful & "Copper deficiency is rare": Though they claim the populace gets plenty of "copper rich" foods, these same foods are known to be rich in sulfur and iron, (Foods Rich in Sulfur). Sulfur binds with copper and removes it from the body, thereby depleting copper status. Note: with the huge selection of foods out there one should consider and question if we have been deceived/programmed into consuming things that were never intended for human consumption -- things that are and always have been toxic to humans. <!--[if !supportLineBreakNewLine]--> <!--[endif]-->
Recommended Daily Allowance (RDA): the RDA for iron is ZERO, while copper has been grossly understated. All the emphasis has been on how vital iron is and how toxic copper is to the body.
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Copper Depleting Poisons: If the food and water supply was untainted, we would not be copper deficient. The main toxin/metal that competes with copper in the body is iron. ALL the food now contains an abundance of iron and iron uptake facilitators that deplete copper status, thereby, replacing copper in the blood and tissues/organs. When copper is not restored during a lifetime, the iron poisoning and accompanying copper deficiency passes down through the generations. The Recommended Daily Allowance (RDA) and Food Pyramid schemes are fraudulent. The requirement for iron is zero while the requirement for copper is grossly understated.
Mercury: A popular ingredient added to MANY foods and beverages is corn syrup, which contains mercury, and is specifically known to deplete copper from the body, and has been positively associated to diabetes prevalence and heart failure, as well as reducing births. (13 & 14)
Supplements: Even "nutritional" supplements are loaded with copper depleting poisons. Note that some are stacked with vitamins, which are not required for supplementation, since the body produces its own. Vitamins deplete copper by facilitating the uptake of iron. One cannot get a copper supplement to boost levels of copper; they have ALL been prepared with other chemicals that negate the copper, or bind the copper to another chemical thereby making it bio-unavailable.
Genetically Damaged ("genetically modified") foods: GMO foods have been around for centuries, referred to as selective breeding, horticulture, and other names. The intent of GMO is to shorten our lifespan by depriving and depleting us of the mineral copper while facilitating and accelerating iron accumulation. Genetically damaged beef: the "Mad Cow" disease that is widespread is from copper deficiency, (10), and illustrates how the entire food chain has been tampered with and depleted of copper. Genetically damaged plant based foods have been modified to increase the iron content or to remove/deactivate the iron uptake inhibitors that were naturally found in the food. Poisoned soils negate/decrease copper availability/uptake, inducing genetic damage to the plant. Plant foods that do not get sufficient copper uptake are genetically damaged. See this page for links regarding genetically damaged foods and iron content. The iron poisoning and accompanied copper deficiency has been ongoing for centuries, starting before colonization began, traced by blood type distribution to country and area of origin, the advent of GMO foods, and significant birth rate increase in the 1500's. (Gestational period decreases as iron poisoning and copper deficiency passes on to the fetus, thereby increasing birth rate.)
Vaccines are loaded with toxins, particularly mercury, that depletes copper from the body, and pathogens that require iron. The mercury specifically targets the liver, where the greatest percentage (~10%) of the body's copper is stored and much of the protein synthesis takes place. Mercury is contained in many if not most vaccines, in addition to food and food chain. The primary accumulation points in the body for mercury are the brain and liver, displacing and depleting copper in those locations, causing massive DNA damage, by disrupting normal protein synthesis. Mercury is very effective and fast-acting in depleting copper, and is apparently a predominant poison in use, as it is contained in a wide variety of sources. The sources include but are not limited to: food, food chain, soft drinks, cereals, cereal bars, teas, soups, sauces, juices, fish, milk/milk products, creams/lotions, toys, jewelry, water, nasal sprays, make-up, lighting, television, computer screens, cell phones, iPods, vaccines, thermometers, batteries, etc. The electronic devices emit toxic mercury vapors, with at least 80% absorption into the blood stream when inhaled. Vaccines were developed to ensure maximum absorption of mercury by transporting directly into the blood stream, thereby by-passing the gut (gastrointestinal tract) where very little is absorbed. Squalene, another vaccine ingredient, comes from the liver of sharks. Sharks are at the top of the fish food chain and contain the highest levels of mercury. (17) Pathogens in vaccines are "dormant" when they are initially planted in the body, but thrive and replicate when the body stores of copper deplete and iron stores increase. This explains the delayed effects or symptoms from vaccines.
The Anthrax Vaccine that has been mandated on military members contains the Anthrax pathogen, which attacks virtually EVERY organ & tissue of the body. The affected organs/areas of the body correlate to the amounts and locations of iron deposits, and copper status. The Anthrax pathogen is deadly, as it apparently has a high survivability and replication rate in the presence of sufficient iron stores and copper deficiency. When they inject the pathogen, they claim it is dead, but it is only dormant at the time of injection. The adjuvant that is added to the vaccine is to deplete liver copper. Squalene adjuvant comes from the liver of sharks, and sharks are at the top of the fish food chain and contain the highest levels of mercury. Mercury quickly and effectively depletes copper from the body, particularly the liver, where much of copper is stored. When the body is invaded by foreign proteins or parasites (“viruses”), copper is quickly mobilized from the liver in order to neutralize, destroy and remove them. The quick depletion of copper from the liver concurrent with parasite/pathogen planting, which is intended by the vaccine, triggers accelerated iron mobilization & accumulation, resulting in immediate or delayed symptoms and ultimately death. Anthrax thrives and replicates very quickly when there are increased iron stores and iron mobilization, and depleted liver copper stores -- the Anthrax pathogen has an affinity for iron.
What is said about the Anthrax vaccine is the same for the other vaccines. They contain pathogens and mercury or another potent copper depleting chemical. Restated, they contain harmful parasites or proteins and an "adjuvant" to expedite copper depletion from the liver. When liver copper is depleted, so is the body's defense mechanism against pathogens.
Radiation is a potent accelerator of iron accumulation and expedites the growth of toxic proteins and viruses, particularly those implanted by the vaccines. Radiation is extremely damaging to the body because it breaks apart the blood proteins, causing vascular damage & accelerating iron deposition. This is how radiation, in addition to other poisons, compromises the blood-brain barrier, by inducing injury to the cerebrovascular system. Copper maintains a balanced pH of 7.00, providing the proper concentration of hydrogen for protein bonds and neutralizing/removing iron. Therefore, since 95% of the population is already severely deficient in copper and iron poisoned, this radiation will quickly deplete what copper is remaining resulting in severe symptoms and subsequent death. In other words, radiation expedites the onset of all the "diseases" and symptoms mentioned previously. Some additional more subtle signs of radiation poisoning (expedited iron deposition): headaches, dizziness, heart palpitations, (any abnormal heart beat), nausea, digestive disturbances, bowel problems, inability to stay asleep, hair loss, loss of pigmentation in hair, any signs of increased or accelerated aging, joint pains, vision and hearing problems, ringing in the ears, irritability, reduced ability to concentrate, short term memory loss, tingling/tightening of the scalp and other parts of the body, dry or brittle skin/hair, increased severity of pre-existing symptoms or disease.
Sources of radiation: Nuclear reactors (positioned in densely populated areas), WI-FI (wireless internet), computers, home security systems, printers, wireless CPU cards, wireless USB modems, wireless routers, airport scanners, television, high power lines, depleted uranium, cell phones, cell towers, mammograms, and other sources of man-made radiation. Cell tower coverage now extends to virtually the entire land mass of the U.S., and other countries. Additionally, WI-FI is installed everywhere now, fast food restaurants,campgrounds, schools, businesses, nursing homes/assisted living centers, overnight accommodations, libraries, universities, airports, flights, and many other places. Tenants unaware of the radiation dangers install wireless devices in most if not all apartment complexes, and if only one tenant gets wireless (WI-FI), everyone else in the building is getting exposed, because the waves travel up to 300 feet (and greater depending on equipment) in all directions. The frequency range for WI-FI encompasses the frequency used by microwave ovens.
The wireless industry is not providing warnings on the dangers of radiation exposure and claim to have no knowledge of these dangers, although there is vast evidence and information to the contrary. Radiation Poisoning of America, RF heating of body tissues and possible DNA alteration (mutation) happens to 100% of the people exposed to RF <!--[if !supportLineBreakNewLine]--> <!--[endif]-->
The Poisoners & Population Reduction: How did they manage to pull off such a successful, massive poisoning campaign, and deceive everyone on the different blood types and diseases They are one entity coordinating & cooperating with many, they possess great wealth, and they have many fronts. They own/control the entire food & water supply, everything that manufactures poisons, and they have a monopoly on the pharmaceutical and wireless industry, and in writing the science and text books. By stealth they successfully add the poisons into the food and water supply, because they control every level and function of our government every agency, organization, the administration, congress, house, all the political parties, FDA, AMA, CDC, USDA, FCC, "naturopathic" and "alternative" health care community, research institutions and foundations, and the list goes on. They have agents and fronts to control us and control what goes into our food and food chain. It's all about control, greed, keeping our minds weak, and decreasing our lifespan. This is how they have been accomplishing their goal of population reduction. It’s about secretly decreasing the population below 200 million – they think by doing so they can change the set times and beat their MAKER.
This is the abomination that causes desolation (depopulation) spoken of through the prophet Daniel.
Their fronts, agencies, and corporations benefit and profit greatly from what they do. Yes, they are all connected that is why they are successful in what they do. Through taxation we pay these people who allegedly represent us, and who give their authority to all these fronts to approve the poisons, without the consent or knowledge of the people. The Constitution does not give authority to our government representatives to lie to us and deceive us, nor does it give authority to the government to act without the consent of the people. The government is supposed to be looking out for the best interests of the people it represents. When this is no longer the case, as we now know, the government ceases to be the rightful, legitimate government, and as such it is time to abolish the entire government.
The poisoners are playing God. They rebel against God and everything that is God and truth. They hate God and they hate the Christ. They are of that line that we've been warned against time and time again, they are of the line that was disinherited 2000 years ago. They do not worship the One and Only True God, our Father in Heaven. They worship that which is evil -- demons, idols, and earthly material things. They are anti-Christ they are many. They are not of the line that authored the books of the Bible. If they were of this line they would adhere to and live by the laws and writings of His servants and the prophets, and would be Christian Jews today. But these Jews are not Christian Jews because they had no hand in writing the Word. (Though, they have tampered with some of the books in order to fulfill their agenda.) In defiance of God they authored their own self fulfilling laws and rituals as found in their books of Talmud and Kabala, those books that go back to an ancient place and time to Babylon. Today they are known as Illuminati, Elite, proponents of their New World Order, and other secret sects and secret societies. These secret groups derive their workings, rituals, symbolism, and traditions from the Talmud and Kabala. They work in secrecy, for the people will be repulsed and angry at what they do. They are liars, murderers, thieves, deceivers, and they destroy the earth and mankind.
They Proclaim To Be God: Remember what you have been told in generations past, for the time has come and the lawless ones have now been revealed. They exalt themselves over everything that is called God or is worshiped, and they set themselves up in God's temple proclaiming to be God, by claiming to be direct descendents of God through the blood --- the blood of Jesus Christ. The blood type found on the Shroud of Turin, the suspected burial cloth of Jesus, is blood type AB, which "matches" the poisoners blood type, and thus, their DNA. Everyone else with blood types of A, B, and O have damaged DNA/proteins . (We were ALL created with blood type AB negative with normal healthy protein/DNA properties; their poisons have mutated us into the other "blood types".) This is how they proclaim to be God, the "Chosen Ones" and the 144,000, by their blood type/DNA matching that found on the Shroud of Turin. They try to change the set times in their favor. Through their secret groups, they perpetuate the blasphemous story of the bloodline of Christ. Their claim is that Jesus fathered a child/children and their ancestors became royalty in Europe and the bloodline now has many descendants. They also claim that everyone else who does not have blood type AB evolved from man-apes ("prehistoric man"), and were not created by God, since the man-apes only have the other major blood types of A, B, and O. This is to glorify themselves and exalt themselves above God and all of creation.
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Added by space wabbit at 8:45am on October 5, 2014
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