I know a few people who have this but bet they will still not listen to alternative News or idea’s and remain sick or die in pain. Iv seen this happen before why are people so brainwashed by the system that lies all the time? Wake up people and be free from death and pain.
The disease of the digestive tract afflicts 400,000 – 600,000 people in North America alone causing abdominal pain, diarrhea (which can be bloody), severe vomiting, weight loss, as well as secondary skin rashes, arthritis, inflammation of the eye, tiredness, and lack of concentration.
Smoking pot caused a “complete remission” of Crohn’s disease compared to placebo in half the patients who lit up for eight weeks, according to clinical trial data to be published the journal Clinical Gastroenterology and Hepatology.
Researchers at Israel’s Meir Medical Center took 21 people with intractable, severe Crohn’s disease and gave 11 of them two joints a day for eight weeks. “The standardized cannabis cigarettes” contained 23 percent THC and 0.5 percent CBD (cannabidiol). (Such marijuana is available on dispensary shelves in San Francisco, Oakland, and other cities that have regulated access to the drug.) The other ten subjects smoked placebo cigarettes containing no active cannabinoids.
Investigators reported that smoking weed caused a “complete remission” of Crohn’s Disease in five of the 11 subjects. Another five of the eleven test subjects saw their Crohn’s Disease symptoms cut in half. Furthermore, “subjects receiving cannabis reported improved appetite and sleep, with no significant side effects.”
The study is the first placebo-controlled clinical trial to assess the consumption of cannabis for the treatment of Crohn’s, notes NORML. All of the patients had intractable forms of the disease and did not respond to conventional treatments. Still, the United States government claims that marijuana is as dangerous as heroin and has no medical use. U.S. Attorney Melinda Haag is waging a war on safe access to medical cannabis in the Bay Area.
One group after another is denouncing the genetically modified poison on grocery store shelves, adding to the chorus of voices demanding real untainted food.
“NFC was very proud to introduce the first “Natural Only” kosher supervision,” said NFC Director Rabbi Reuven Flamer. “It’s a logical application of our principle, ‘Start Naturally. Stay that Way.’ Therefore, the Natural Apple K cannot be placed on a product that contains GMOs,” Flamer explained.
“While according to the strict letter of Kosher food law a GMO food ingredient is not prohibited, in our view it is not natural. Additionally, there is a Torah (religious)-based law to ‘guard your health’. GMOs are the number-one growing concern among health-conscious consumers and for businesses in the natural and organic food market, as well as in the conventional food industry,” said Rabbi Flamer.
“Recent studies show that GMOs may cause various kinds of health problems from digestive disturbances to food allergies, and that GMOs require more herbicides, which is really the opposite reason why GMOs were touted to be so environmentally helpful in the first place,” Rabbi Flamer added. “For all of the many reasons that GMOs raise a red flag, consumers simply don’t want them in their foods, and our clients want to accommodate their customers.”
Over the next 12 months, the company will phase out the certification of any product that contains GMO ingredients, and will no longer accept applications for certification of products that contain GMOs.
NFC has numerous natural food certification programs, including USDA Organic certification, Kosher certification (under the “Apple K” label), Vegan certification, and Gluten Guard, a gluten-free assurance program.
Each product submitted by a manufacturer for approval is carefully analyzed. The press release explains the process for all of the certification categories. ”The process may include, but is not limited to, a request and review of the ingredient deck including country of origin andcertificate of analysis, product testing, as well as inspection of manufacturing facilities.”
Whether or not your faith requires you to follow the Kosher food laws, this news should be celebrated by anyone who hopes to see the demise of Monsanto and the products created by their mad scientists. While countries across the world are banning GMOs, the wheels are moving slowly in North America to even have GMOs labeled so that consumers can make an informed decision. To have a large demographic refuse to allow genetically modified material in their food is yet another volley against the corruption that is evident in the unholy alliance of the FDA and Monsanto.
The Kombucha recipe for mushroom tea is fun and easy. Kombucha tea is said to be a powerful aid to the body’s natural cleansing process.
The Kombucha mushroom tea is a boost to the immune system and a proven prophylactic against cancer and other degenerative diseases because of the glucuronic acid of the Kombucha tea.
The Kombucha “mushroom” (which is actually a symbiotic colony of yeast and bacteria) acts on sugar and tea to produce not only acetic and lactic acid but also small amounts of a potent detoxifying substance, glucuronic acid.
Normally this organic acid is produced by the liver in sufficient quantities to neutralize toxins in the body. These toxins are either naturally produced toxins or poisons ingested in food and water.
When the body must deal with a super abundance of toxins from the environment the liver functions become overloaded. This is certainly the case with most of us today.
Additional glucuronic acid taken in the form of Kombucha Tea is said to be a powerful aid to the body’s natural cleansing process, a boost to the immune system and a proven prophylactic against cancer and other degenerative diseases.
1. Bring to a Boil 3+ quarts good water. (Filtered water) (2.84 Liters)
2. Add Sugar 1 – 3 cups Sugar (I usually use 2 cups)
3. Bring to boil and boil 5 minutes
4. Turn the heat off
5. Add 2-Green Tea bags plus 4-5 black tea bags for a total of 5-7 tea bags, or 2-3 tsp. loose tea usually 15 grams
6. Steep 10 minutes.
7. Remove tea bags
8. Allow to cool to room temperature
9. Keep covered and careful of contamination at this stage as the brew is a highly Sweet and Appetizing
10. Be sure everything is at the same temperature
11. Pour cooled, room temperature liquid into fermenting container
(gallon jar with wide mouth).
12. Add 2 cups Previously Fermented Kombucha Brew as a Starter.
13. Add Kombucha Mushroom (which is also at room temperature)
14. Cover with a clean cloth, paper towel or coffee filter. Set the jar of Kombucha aside in a quiet undisturbed spot. Every time the liquid is disturbed the mushroom will begin to start forming over again and not form properly. However the kombucha tea may still be good.
15. Ferment. 6 – 8 days (normal brew cycle) at 80F constant temperature, (8-14 days in the 70’s). Below 65F is not recommended. First time may take longer. Temperature Range: 68-83 degrees Fahrenheit. (20 – 26 degrees Centigrade)
Kombucha Tea should be sparkling, semi-sweet, cidery taste. The pH 2.7 to 3.2.
IMPORTANT! Save (Decanter) 1-2 cups (8-16 oz/240-500 ml) to begin another batch.
Each batch should produce another mushroom.
Save one mushroom, covered with Kombucha Tea and safely stored in the refrigerator, in the event of some disaster. Use either mushroom to start another batch. You may also give a mushroom to friends and introduce them to a great healthy drink.
Have fun.
I drink a ½ glass of Kombucha tea in the morning and sometimes in the late afternoon. My appetite is curbed and I feel energized.
Kombucha is a refreshing drink that removes the toxins from my liver. Kombucha is easy to make in the home and aids in treating cancer alternatively.
The medical science is strongly in favor of THC laden hemp oil as a primary cancer therapy, not just in a supportive role to control the side effects of chemotherapy.
The International Medical Veritas Association (IMVA) is putting hemp oil on its cancer protocol. It is a prioritized protocol list whose top five items are magnesium chloride, iodine, selenium,Alpha Lipoic Acid and sodium bicarbonate. It makes perfect sense to drop hemp oil right into the middle of this nutritional crossfire of anti cancer medicines, which are all available without prescription.
Hemp oil has long been recognised as one of the most versatile and beneficial substances known to man. Derived from hemp seeds (a member of the achene family of fruits) it has been regarded as a superfood due to its high essential fatty acid content and the unique ratio of omega3 to omega6 and gamma linolenic acid (GLA) – 2:5:1. Hemp oil, is known to contain up to 5% of pure GLA, a much higher concentration than any other plant, even higher than spirulina. For thousands of years, the hemp plant has been used in elixirs and medicinal teas because of its healing properties and now medical science is zeroing in on the properties of its active substances.
Both the commercial legal type of hemp oil and the illegal THC laden hemp oil are one of the most power-packed protein sources available in the plant kingdom. Its oil can be used in many nutritional and transdermal applications. In other chapters in my Winning the War on Cancer book we will discuss in-depth about GLA and cancer and also the interesting work of Dr. Johanna Budwig. She uses flax seed oil instead of hemp oil to cure cancer – through effecting changes in cell walls – using these omega3 and omega6 laden medicinal oils.
Actually there is another way to use medical marijuana without smoking the leaf. According to Dr. Tod H. Mikuriya, “The usual irritating and toxic breakdown products of burning utilized with smoking are totally avoided with vaporization. Extraction and inhaling cannabinoid essential oils below ignition temperature of both crude and refined cannabis products affords significant mitigation of irritation to the oral cavity, and tracheobronchial tree from pyrollytic breakdown products.[iii]
Rick Simpson, the man in the documentary below, has been making hemp oil and sharing it with friends and neighbors without charging for it. In small doses, he says, it makes you well without getting you high. “Well you can’t deny your own eyes can you?” Simpson asks. “Here’s someone dying of cancer and they’re not dying anymore. I don’t care if the medicine comes from a tomato plant, potato plant or a hemp plant, if the medicine is safe and helps and works, why not use it?” he asks.
When a person has cancer and is dying this question reaches a critical point. The bravery of Rick Simpson from Canada in showing us how to make hemp oil for ourselves offers many people a hope that should be increasingly appreciated as money dries up for expensive cancer treatments. We are going to need inexpensive medicines in the future and there is nothing better than the ones we can make reasonably cheaply ourselves.
For most people in the world it is illegal so the choice could come down to breaking the law or dying. There is no research to indicate what advantages oral use of hemp oil vs. vaporization but we can assume that advantage would be nutritional with oral intake. Dr. Budwig Below work would sustain this point of view especially for cancer patients.
The Science
According to Dr. Robert Ramer and Dr. Burkhard Hinz of the University of Rostock in Germany medical marijuana can be an effective treatment for cancer.[v] Their research was published in the Journal of the National Cancer Institute Advance Access on December 25th of 2007 in a paper entitled Inhibition of Cancer Cell Invasion by Cannabinoids via Increased Expression of Tissue Inhibitor of Matrix Metalloproteinases-1.
The biggest contribution of this breakthrough discovery, is that the expression of TIMP-1 was shown to be stimulated by cannabinoid receptor activation and to mediate the anti-invasive effect of cannabinoids. Prior to now the cellular mechanisms underlying this effect were unclear and the relevance of the findings to the behavior of tumor cells in vivo remains to be determined.
Marijuana cuts lung cancer tumor growth in half, a 2007 Harvard Medical School study shows.[vi] The active ingredient in marijuana cuts tumor growth in lung cancer in half and significantly reduces the ability of the cancer to spread, say researchers at Harvard University who tested the chemical in both lab and mouse studies.
This is the first set of experiments to show that the compound, Delta-tetrahydrocannabinol (THC), inhibits EGF-induced growth and migration in epidermal growth factor receptor (EGFR) expressing non-small cell lung cancer cell lines. Lung cancers that over-express EGFR are usually highly aggressive and resistant to chemotherapy. THC that targets cannabinoid receptors CB1 and CB2 is similar in function to endocannabinoids, which are cannabinoids that are naturally produced in the body and activate these receptors.
“The beauty of this study is that we are showing that a substance of abuse, if used prudently, may offer a new road to therapy against lung cancer,” said Anju Preet, Ph.D., a researcher in the Division of Experimental Medicine. Acting through cannabinoid receptors CB1 and CB2, endocannabinoids (as well as THC) are thought to play a role in variety of biological functions, including pain and anxiety control, and inflammation.
Researchers reported in the August 15, 2004 issue of Cancer Research, the journal of the American Association for Cancer Research, that marijuana’s constituents inhibited the spread of brain cancer in human tumor biopsies.[vii] In a related development, a research team from the University of South Florida further noted that THC can also selectively inhibit the activation and replication of gamma herpes viruses. The viruses, which can lie dormant for years within white blood cells before becoming active and spreading to other cells, are thought to increase one’s chances of developing cancers such as Kaposi’s Sarcoma, Burkitt’s lymphoma and Hodgkin’s disease.[viii]
In 1998, a research team at Madrid’s Complutense University discovered that THC can selectively induce programmed cell death in brain tumor cells without negatively impacting surrounding healthy cells. Then in 2000, they reported in the journal Nature Medicine that injections of synthetic THC eradicated malignant gliomas (brain tumors) in one-third of treated rats, and prolonged life in another third by six weeks.[ix]
Led by Dr. Manuel Guzman the Spanish team announced they had destroyed incurable brain cancer tumors in rats by injecting them with THC. They reported in the March 2002 issue of “Nature Medicine” that they injected the brains of 45 rats with cancer cells, producing tumors whose presence they confirmed through magnetic resonance imaging (MRI). On the 12th day they injected 15 of the rats with THC and 15 with Win-55,212-2 a synthetic compound similar to THC.[x]
Researchers at the University of Milan in Naples, Italy, reported in the Journal of Pharmacology and Experimental Therapeutics that non-psychoactive compounds in marijuana inhibited the growth of glioma cells in a dose-dependent manner, and selectively targeted and killed malignant cells through apoptosis. “Non-psychoactive CBD produce[s] a significant anti-tumor activity both in vitro and in vivo, thus suggesting a possible application of CBD as an antineoplastic agent.”[xi]
The first experiment documenting pot’s anti-tumor effects took place in 1974 at the Medical College of Virginia at the behest of the U.S. government. The results of that study, reported in an Aug. 18, 1974, Washington Post newspaper feature, were that marijuana’s psychoactive component, THC, “slowed the growth of lung cancers, breast cancers and a virus-induced leukemia in laboratory mice, and prolonged their lives by as much as 36 percent.”[xii]
Funded by the National Institute of Health to find evidence that marijuana damages the immune system, found instead that THC slowed the growth of three kinds of cancer in mice — lung and breast cancer, and a virus-induced leukemia. The DEA quickly shut down the Virginia study and all further cannabis/tumor research even though the researchers “found that THC slowed the growth of lung cancers, breast cancers and a virus-induced leukemia in laboratory mice, and prolonged their lives by as much as 36 percent.”
“Antineoplastic Activity of Cannabinoids,” an article in a 1975 Journal of the National Cancer Institute reports, “Lewis lung adenocarcinoma growth was retarded by the oral administration of tetrahydrocannabinol (THC) and cannabinol (CBN)” — two types of cannabinoids, a family of active components in marijuana. “Mice treated for 20 consecutive days with THC and CBN had reduced primary tumor size.”
Marijuana relieves pain that narcotics like morphine and OxyContin
have hardly any effect on, and could help ease suffering from
illnesses such as multiple sclerosis, diabetes and cancer.[xiii]
According to Devra Davis in her book Secret History of the War on Cancer, 1.5 million lives have been lost because Americans failed to act on existing knowledge about the environmental causes of cancer. It is impossible to calculate the added deaths from suppressed ‘cancer cures’ but we do know of the terrible suffering of hundreds of thousands of people who have been jailed for marijuana use.
Hemp oil with THC included has the making of a primary cancer treatment, which even alone seems to have a great chance of turning the tide against cancer tumors. It has the added advantage of safety, ease of use, lack of side effects and low cost if one makes it oneself. Surrounded by other medicinal anti-cancer substances in a full protocol it’s hard to imagine anyone failing and falling in their war on cancer.
THC should be included in every cancer protocol.
Sodium bicarbonate is another excellent anti tumor substance that reduces tumors but is much more difficult to administer than THC hemp oil. Cannabinoids are able to pass through all barriers in the body like Alpha Lipoic Acid so simple oral intake is sufficient. With bicarbonate we need intravenous applications and often even this is not sufficient, often we have to use catheters and few doctors in the world are willing to administer this way.
In the end all cancer treatments that are not promoted by mainstream oncology are illegal. No licensed doctor is going to claim that are curing cancer with sodium bicarbonate though they will treat people with cancer explaining they are balancing pH or some other metabolic profile with this common emergency room medicine found also most kitchens of the world. More than several states have passed laws making medical marijuana legal but the federal government will not relax and let people be free to choose their treatments even if their lives depend on it.
Davis notes that the cowardice of research scientists, who publish thoroughly referenced reports but pull their punches at the end, by claiming that more research needs to be done before action can be taken. Statements like these are exploited by industry that buys time to make much more money. It is a deliberate attempt that creates wholesale public doubt from small data gaps and remaining scientific uncertainties.
They have done that with everything right up to and including sunlight. Everything is thought to be dangerous except the pharmaceutical drugs which are the most dangerous substances of all. Stomach wrenching chemotherapy and the death principle of radiation are legal yet safe THC laden hemp oil is not.
It is legal for doctors to attack people with their poisons but you can go to jail for trying to save yourself or a loved one from cancer with the oil of a simple garden weed. Our civilization has put up with this insanity but there is a great price being paid. In a mad medical world people die that need not and this is a terrible sadness that has destroyed the integrity and ethics of modern medicine.
The science for the use of hemp oil is credible, specific fact-based, and is documented in detail.[xiv] There is absolutely no reason to not legalize medical marijuana and create an immediate production and distribution of THC hemp oil to cancer patients. Unfortunately we live in a world populated with governments and medical henchmen who would rather see people die cruel deaths then have access to a safe and effect cancer drug.
Meanwhile the Food and Drug Administration approved Genentech’s best-selling drug, Avastin, as a treatment for breast cancer, in a decision, according to the New York Times, “that appeared to lower the threshold somewhat for approval of certain cancer drugs. The big question was whether it was enough for a drug temporarily to stop cancer from worsening — as Avastin had done in a clinical trial — or was it necessary for a drug to enable patients to live longer, which Avastin had failed to do. Oncologists and patient advocates were divided, in part because of the drug’s sometimes severe side effects.”[xv]
The differences between Avastin and hemp oil are huge. First Avastin will earn Genentech hundreds of millions where THC hemp oil will earn no one anything. Second there are no severe or even mild side effects to taking hemp oil and lastly it is not a temporary answer but a real solution. Certainly hemp oil will ensure a longer life.
The chemistry of dichloroacetic acid is typical for halogenatedorganic acids. It is a member of the chloroacetic acids family. The dichloroacetate ion is produced when the acid is mixed with water. As an acid with a pKa of 1.35,[1] pure dichloroacetic acid is verycorrosive and extremely destructive to tissues of the mucous membranes and upper respiratory tract.[2]
Owing to the highly corrosive action of the acid, only the salts of dichloroacetic acid are used therapeutically, including its sodium and potassium salts, sodium dichloroacetate and potassium dichloroacetate.
A randomized controlled trial in children with congenital lactic acidosis found that while DCA was well tolerated, it was ineffective in improving clinical outcomes.[6] A separate trial of DCA in children with MELAS (a syndrome of inadequate mitochondrial function, leading to lactic acidosis) was halted early, as all 15 of the children receiving DCA experienced significant nerve toxicity without any evidence of benefit from the medication.[7] A randomized controlled trial of DCA in adults with lactic acidosis found that while DCA lowered blood lactate levels, it had no clinical benefit and did not improve hemodynamicsor survival.[8]
Thus, while early case reports and pre-clinical data suggested that DCA might be effective for lactic acidosis, subsequent controlled trials have found no clinical benefit of DCA in this setting. In addition, clinical trial subjects were incapable of continuing on DCA as a study medication owing to progressive toxicities.
Cancer cells generally express increased glycolysis, because they rely on anaerobic respiration that occurs in the cytosol (lactic acid fermentation) rather than oxidative phosphorylation in the mitochondria for energy (the Warburg effect), as a result of hypoxia that exists in tumors and malfunctioning mitochondria.[9][10] Usually dangerously damaged cells kill themselves via apoptosis, a mechanism of self-destruction that involves mitochondria, but this mechanism fails in cancer cells.
A phase I study published in January 2007 by researchers at the University of Alberta, who had tested DCA on human[11] cancer cells grown in mice, found that DCA restored mitochondrial function, thus restoring apoptosis, allowing cancer cells to self-destruct and shrink the tumor.[12]
These results received extensive media attention, beginning with an article in New Scientist titled “Cheap, ‘safe’ drug kills most cancers”.[11] Subsequently, the American Cancer Society and other medical organizations have received a large volume of public interest and questions regarding DCA.[13]Clinical trials in humans with cancer have not been conducted in the USA and are not yet final in Canada, emphasizing the need for caution in interpreting the preliminary results.[13][14]
In in vitro studies, Evangelos Michelakis of University of Alberta found that in tissue samples from 49 patients, DCA caused depolarization of mitochondria in GBM tissue but not in healthy brain tissue.[15]
Five palliative patients with primary GBM were entered into a phase II trial. Three had not responded to several chemotherapies; two were newly diagnosed. After surgical removal of tumor mass, they were treated with DCA and chemotherapy.[15]
Of the five patients tested, one died after three months. The surviving four were followed for 15 months. Their Karnofsky scores were unchanged in two cases, and decreased by 10 points in two patients.[15]
DCA was associated with tumor regression and had a good safety profile. DCA side effects were minimal.[15]
Michelakis is proceeding with phase three human studies with private funding from philanthropic groups and individuals. DCA’s legal status as a discovery is public domain because it was made or discovered as far back as 1864[16] and has been used in the treatment of canine and human lactic acidosis, some who presented at the beginning of treatment with cancer.
Following its initial publication, The New Scientist later editorialized, “The drug may yet live up to its promise as an anti-cancer agent – clinical trials are expected to start soon. It may even spawn an entirely new class of anti-cancer drugs. For now, however, it remains experimental, never yet properly tested in a person with cancer. People who self-administer the drug are taking a very long shot and, unlikely as it may sound, could even make their health worse.”[17]
In 2010, it was found that for human colorectal tumours grown in mice, under hypoxic conditions, DCA decreased rather than increased apoptosis, resulting in enhanced growth of the tumours.[18] These findings suggest that at least in some cancer types DCA treatment could be detrimental to patient health, highlighting the need for further testing before it can be considered a safe and effective cancer treatment.[18]
DCA is non-patentable as a compound, though a patent has been filed for its use in cancer treatment.[19] Research by Evangelos Michelakis has received no support from the pharmaceutical industry.[20] Concerns have been raised that without strong intellectual property protection, the financial incentive for drug development is reduced, and therefore obtaining sufficient funds to conduct clinical trials presents difficulty.[11][13][14][21] However, other sources of funding exist; previous studies of DCA have been funded by government organizations such as the National Institutes of Health, the Food and Drug Administration, the Canadian Institutes of Health Researchand by private charities (e.g. the Muscular Dystrophy Association). Recognizing anticipated funding challenges, Michelakis’s lab took the unorthodox step of directly soliciting online donations to fund the research.[22] After 6 months, his lab had raised over $800,000, enough to fund a small Clinical Phase 2 study. Michelakis and Archer have applied for a patent on the use of DCA in the treatment of cancer.[19][23]
On 24 September 2007, the Department of Medicine of Alberta University reported that after the trial funding was secured, both the Alberta local ethics committee and Health Canada approved the first DCA clinical trial for cancer.[24] This initial trial was relatively small with enrollment of up to 50 patients. The trial was completed in August 2009.[25] In May 2010 the team published a press release[26]stating no conclusions could be drawn as a result of the trial. A paper describing the results was published[27] but not linked from the press release. Only five patients had been treated with the drug during the trial.
In May 2011, online reports[28] suggested that the Alberta group had released new data which the media “had not reported”. However, this appeared to be caused by confusion between dates (the previous update was May 2010[29]) and cancer charities moved quickly to counter these rumours,[30][31] which were subsequently covered in New Scientist magazine.[32]
The use of this compound as an anti-cancer agent has been patented.[33]
Reports in the lay press after the 2007 University of Alberta announcement claim that dichloroacetate “has actually been used safely in humans for decades”,[34] DCA is generally well tolerated, even in children.[35] Short-term, infused, bolus doses of DCA at 50 mg/kg/day have been well tolerated.[36]
A clinical trial where DCA was given to patients of MELAS (a form of genetically inherited lactic acidosis) at 25 mg/kg/day was ended prematurely due to excessive peripheral nerve toxicity.[38] Dichloroacetate can also have anxiolytic or sedative effects.[3]
Animal studies suggest that the neuropathy and neurotoxicity during chronic dichloroacetate treatment may be partly due to depletion of thiamine, and thiamine supplementation in rats reduced these effects.[39] However, more recent studies in humans suggest that peripheral neuropathy is a common side effect during chronic DCA treatment, even with coadministration of oral thiamine.[40][41] An additional study reported that 50 mg/kg/day DCA treatment resulted in unsteady gait and lethargy in two patients, with symptoms occurring after one month for one patient and two months for the second. Gait disturbance and consciousness were recovered with cessation of DCA, however sensory nerveaction potentials did not recover in one month.[42]
It has been reported that animals and patients treated with DCA have elevated levels of delta-aminolevulinic acid (delta-ALA) in the urine. A study published in 2008 suggests that this product may be the cause of the neurotoxic side effect of DCA by blocking peripheralmyelin formation.[43]
Long term use (three years or more) of high doses (> 77 mg/kg/day) of DCA has been shown to increase risk of liver cancer in mice.[37]Studies of the trichloroethylene (TCE) metabolites dichloroacetic acid (DCA), trichloroacetic acid (TCA), and chloral hydrate suggest that both DCA and TCA are involved in TCE-induced liver tumorigenesis and that many DCA effects are consistent with conditions that increase the risk of liver cancer in humans.[44] It should be noted here that the maximum recommended dose for cancer treatment is 20mg/kg/day (less than 1/3rd of the 77mg/kg/day shown to increase liver cancer risk in mice).
The promise of DCA as a cheap, effective and safe treatment for cancer generated a great deal of public interest. Many people turned to self-medication.[45][46]
Doctors warned of potential problems if people attempt to try DCA outside a controlled clinical trial. “If it starts going badly, who is following you before it gets out of control? By the time you realize your liver is failing, you’re in big trouble”, said Laura Shanner, Associate Professor of Health Ethics at the University of Alberta.[47]
^ Stacpoole P, Lorenz A, Thomas R, Harman E (1988). “Dichloroacetate in the treatment of lactic acidosis”. Ann Intern Med108 (1): 58–63. PMID3337517.
^ ab Stacpoole P, Kerr D, Barnes C, Bunch S, Carney P, Fennell E, Felitsyn N, Gilmore R, Greer M, Henderson G, Hutson A, Neiberger R, O’Brien R, Perkins L, Quisling R, Shroads A, Shuster J, Silverstein J, Theriaque D, Valenstein E (2006). “Controlled clinical trial of dichloroacetate for treatment of congenital lactic acidosis in children”. Pediatrics117 (5): 1519–1531. doi:10.1542/peds.2005-1226 . PMID16651305.
^ ab Kaufmann P, Engelstad K, Wei Y, Jhung S, Sano M, Shungu D, Millar W, Hong X, Gooch C, Mao X, Pascual J, Hirano M, Stacpoole P, DiMauro S, De Vivo D (2006). “Dichloroacetate causes toxic neuropathy in MELAS: a randomized, controlled clinical trial”. Neurology66 (3): 324–330.doi:10.1212/01.wnl.0000196641.05913.27 .PMID16476929.
^ ab Stacpoole P, Wright E, Baumgartner T, Bersin R, Buchalter S, Curry S, Duncan C, Harman E, Henderson G, Jenkinson S (1992). “A controlled clinical trial of dichloroacetate for treatment of lactic acidosis in adults. The Dichloroacetate-Lactic Acidosis Study Group”. N Engl J Med327 (22): 1564–1569.doi:10.1056/NEJM199211263272204 . PMID1435883.
^ Xu R, Pelicano H, Zhou Y, Carew J, Feng L, Bhalla K, Keating M, Huang P (2005). “Inhibition of glycolysis in cancer cells: a novel strategy to overcome drug resistance associated with mitochondrial respiratory defect and hypoxia”. Cancer Res65(2): 613–21. PMID15695406.
^ Bonnet, Sébastien; Archer, Stephen L.; Allalunis-Turner, Joan; Haromy, Alois; Beaulieu, Christian; Thompson, Richard; Lee, Christopher T.; Lopaschuk, Gary D. et al. (2007). “A Mitochondria-K+ Channel Axis Is Suppressed in Cancer and Its Normalization Promotes Apoptosis and Inhibits Cancer Growth”. Cancer Cell11 (1): 37–51.doi:10.1016/j.ccr.2006.10.020 . PMID17222789.
^US 8071645 , Newell, M. Karen; Newell, Evan & Villalobos-Menuey, Elizabeth, “Systems and methods for treating human inflammatory and proliferative diseases and wounds, with fatty acid metabolism inhibitors and/or glycolytic inhibitors”
^ Pearson H; Kurtz, TL; Han, Z; Langaee, T (2008). “Role of dichloroacetate in the treatment of genetic mitochondrial diseases”. Adv Drug Deliv Rev.60 (13,14): 1478–1487.doi:10.1016/j.addr.2008.02.014 . PMID18647626.
^ Agbenyega T, Planche T, Bedu-Addo G, Ansong D, Owusu-Ofori A, Bhattaram VA, Nagaraja NV, Shroads AL, Henderson GN, Hutson AD, Derendorf H, Krishna S, Stacpoole PW (2003). “Population kinetics, efficacy, and safety of dichloroacetate for lactic acidosis due to severe malaria in children”. J Clin Pharmacol.43 (4): 386–396.doi:10.1177/0091270003251392 . PMID12723459.
^ ab DeAngelo AB, Daniel FB, Stober JA, Olson GR (1991). “The carcinogenicity of dichloroacetic acid in the male B6C3F1 mouse”. Fundam Appl Toxicol.16 (2): 337–347.doi:10.1016/0272-0590(91)90118-N . PMID2055364.
^ Kaufmann P, Engelstad K, Wei Y et al. (2006). “Dichloroacetate causes toxic neuropathy in MELAS: a randomized, controlled clinical trial”. Neurology66 (3): 324–330. doi:10.1212/01.wnl.0000196641.05913.27 .PMID16476929.
^ Stacpoole P, Harwood H, Cameron D, Curry S, Samuelson D, Cornwell P, Sauberlich H (1990). “Chronic toxicity of dichloroacetate: possible relation to thiamine deficiency in rats”.Fundam Appl Toxicol14 (2): 327–37. doi:10.1016/0272-0590(90)90212-3 . PMID2318357.
^ Kurlemann G, Paetzke I, Moller H, Masur H, Schuierer G, Weglage J, Koch HG (1995). “Therapy of complex I deficiency: peripheral neuropathy during dichloroacetate therapy”. Eur J Pediatr154 (11): 928–32. doi:10.1007/BF01957508 .PMID8582409.
^ Spruijt L, Naviaux RK, McGowan KA, Nyhan WL, Sheean G, Haas RH, Barshop BA (2001). “Nerve conduction changes in patients with mitochondrial diseases treated with dichloroacetate”. Muscle Nerve24 (7): 916–24.doi:10.1002/mus.1089 . PMID11410919.
^ Oishi K, Yoshioka M, Ozawa R, Yamamoto T, Oya Y, Ogawa M, Kawai M (2003). “Dichloroacetate treatment for adult patients with mitochondrial disease”. Rinsho Shinkeigaku43 (4): 154–61. PMID12892050.
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Recent Medical Research at a Canadian University has confirmed that scientists do understand the cause of cancer. The dying off of old cells to be replaced by new cells is a normal part of our cellular lifecycle and keeps us well. It seems that in cancerous cells, our body has forgotten how to tell the aged cells how to die off and be replaced by healthy new cells. This process is governed by the mitochondria and is known as “cell death” or “apoptosis”. In a cancer cell, the mitochondria has lost the ability to direct the cell to die off – the sick cell becomes “immortal”, spreading and making the person increasingly unwell. Recent Medical trials using Pure DCA have proven this compound can reactivate the mitochondria restoring the cell’s original function of “apoptosis” enabling shrinkage in tumor size and mass. Testimonials have shown reversal in illness, remission, clean health tests, increased health and vitality. Favourable results (scientifically measurable) have been accomplished within days (less than a week) of starting treatment with Pure DCA.
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Below you can find a description of the main sections of this website.
Dichloroacetate has been used in recent human trials and was found to shrink tumors. These trials were done by a university and their results have been published for anyone to read about the dichloroacetate cancer connection. The link to the universities dichloroacetate study.
After reviewing just the basic programs that you need to operate a smart phone…when you go to applications, for example and look at google mail..it states they have right to go into your mail, look at your documents and alter (even if it is confidential) , change your contacts or even delete contacts, have access to your text message and pictures, they can even use your text and phone to call and send messages. So with that said…they have access to your mail by default because you have to use that program on your phone to be activated for most functions on your phone to work properly.
If you go through all the programs you have on your phone before adding more apps, they all say pretty much the same thing. But look at the big picture…where are these phone made (China, Japan, Korea)! Government employees are using these phones just as much as anyone else..what can be worse then countries that are making these phones have access to sensitive material including personal information that can be of use in sensitive ways including…where they are, their pictures, their contacts and their email documents.
Now your family members are adding app after app with location settings needing to be active on the devices for them to be of service. With that said there is apps and even programs that someone can see all cell phones in that area so a possible predator can single out possible victims. What about some family members who take pictures of their drivers license, SSN and other highly personal information for identity theft to be easy..not alone..logging into bank accounts..in which you are allowing the manufacture to have access to with your passwords and all. Also think about this, these apps also are being allowed to turn on your video camand recorder on your cell at any given time to listen and look at your surroundings. They do not have to inform you when they do, what they alter or delete or whom they give your information to. Also keep in mind that a lot of the apps are created by criminals that are making it legal to commit crimes against you by just getting their free app.So the matter of this news story, if we buy these cell phones from a company ..just say Sprint, shouldn’t they be liability for use licensing with the apps for the purpose of the basic operation of the phone and not carried over to us making ourselves liable for any misuse of our privacy in which will will not know? Should the consumer buying the cell phone have licensing right to know when an invasion by the app provider went into the phone and made changes?
For another quick check of what your allowing your cell phone maker to do to you…go to settings, then look at what system your phone uses..Android system for example, click that and read of the privacy you no longer have!
Let me not to forget to mention the negative heath effects Cell phones can have on your body because of the radiation-emitting device inside of cell phones that allow it to transmit the communication signals
If you’re an avid cell phone user who refuses to believe that holding this radiation-emitting device next to your head poses a potential health risk, take note…
Italy‘s supreme court has ruled that a man’s brain tumor is, in fact, linked to his heavy cell phone use.
The court’s assessment included studies by Professor Lennart Hardell of Sweden, stating they had more cases, involved long-term use and were independent (as opposed to Interphone’s industry funding). Hardell has found that those who begin using cell phones heavily as teenagers have 4 to 5 times more brain cancer as young adults!
Just 50 Minutes of Cell Phone Use Alters Your Brain
Even if you don’t use a cell phone for hours each day, research by leading brain imaging researcher Nora D. Volkow, MD of the National Institutes of Health, revealed that after just 50 minutes of cell phone exposure, the emitted radiation increases brain cell activity in the region closest to the cell phone antenna.1 The exact health effects of that increased brain activity are as of yet unknown, but the study effectively debunked the myth in U.S. government research circles that cell phone radiation at non-thermal levels is incapable of causing biological change.
So keep using your cell phone if you don’t give a crap about your health and the Antichrist NWO Global Government spying on you. And when your sitting in a NDDA Death Camp don’t call me to get you out and fix your brain. I tried to tell you but you didn’t listen you brainwashed boot licking Zombie’s
Could it be that the current bed bug infestation is a sign of the End Times? Perhaps a prelude to 2012? Maybe it’s just another thing we can blame Bush or Obama about? Oddly enough, the White House has developed a serious problem of insect infestation ever since Obama moved in.
A good conspiracy theory focuses us Plum Island, New York. A facility there allegedly run by the Department of Agriculture researches animal diseases. However, many believe that it was the site of a Cold War era biological weapon laboratory. Oddly enough, the Army transferred control of Plum Island to the DoA in the early 1950s following an outbreak of foot-and-mouth disease amongst cattle. Since then, some conspiracy experts point to outbreaks of Lyme disease and other bizarre experiments. In the film, “Silence of the Lambs”, the evil Hannibal Lecter called Plum Island “Anthrax Island”.
In 2002, the facility was curiously turned over to control under the Department of Homeland Security. Plum Island was even linked to a potential Al Qaeda terror plot when Aafia Siddiqui, a Pakistani scientist, was arrested in 2008. She was found to have a list of “mass casualty attack” targets, with Plum Island as one of the locations.
Perhaps even more strange is the weird story of the Montauk Monster, started when the carcass of an unidentified creature washed up on shore. Later, the body of a possible human also washed up on shore. The deformed humanoid was said to have a series of five holes drilled into it’s skull, as if part of an experiment. Montauk has also been associated with other conspiracies, ranging from government psychic research to time travel and even inter-dimensional beings. The infamous ‘Montauk Chair’ is said to be part of a U.S. government experiment with alien technology from crashed UFOs.
So what does this have to do with the bed bugs concern? With the current bed bugs infest of homes, apartments, officebuildings and historic hotels like the Waldorf-Astoria? Bed bugs may be part of another experiment gone awry from Plum Island. Perhaps even part of the alleged New World Order plan to reduce the human population to below 500 million people, as depicted on the strange and infamous America’s ‘Stonehenge’, more commonly known as the ‘Georgia Guidestones’. A granite monument which calls for a one-world government and depopulation of the planet of humanity. Are bed bugs, stink bugs and other infestations this year part of such a plan? Who can say?
If you have bed bugs, you can be eaten alive from head to toe. Besides this, there are many psychological effects. Many people are repulsed by people who have bed bugs. This can be extremely humiliating and can subject you to social stigma. Friends can stop visiting and also inviting you to parties. You can be left alone and completely ashamed. It can turn your life completely upside down.
Even in a nice hotel like Vegas, you can be subjected to bed bug bites. This is an infestation problem in the United States, and it can make people feel extremely ashamed. It is similar to the mental disease that can make someone turn into a recluse and a hoarder. It is possible that you simply shouldn’t tell anyone, unless you have the problem taken care of. Honesty may be the best policy, but that will come with a tremendous social cost. Even people at your work will want to stay away from you because they will not want to come near you.
If you stay in a hotel, you should avoid placing your luggage on the bed.
(NaturalNews) Astragalus is a traditional Chinese medicinal herb that has been around for over 4,000 years. Astragalus is an adaptogenic, nontoxic herb and plant extract that helps the body resist the damaging effects of stress while restoring normal physiological function. Astragalus aids adrenal function, digestion, metabolism, combats fatigue and increases stamina. Astragalus is very effective in helping people with AIDS and has even proven to have an anti-tumor effect and can increase the efficacy of chemotherapy.
A native plant of China, astragalus is officially known as astragalus membranaceus: AKA Milk Vetch Root and Huang Qi. Astragalus is a perennial plant that grows up to 4 feet tall. The root of the plant has a sweet taste and contains choline, flavonoids, amino acids-gamma aminobutyric acid, canavanine, beta-sitosterol, saponins (astragalosides) and oil. The primary actions of astragalus are adaptogenic and immunomodulating. The secondary actions are anti-inflammatory, anti-viral, cardiotonic, diuretic and hepatoprotective.
Medicinal Use
Astragalus is an herb that has actions in nearly all of the body systems. It is used to treat chronic colds, Epstein Barr Virus, HIV and candida by preventing infection recurrence. Astragalus stimulates bone marrow blood cells while enhancing deep immune strength. Studies show that the polysaccharides in astragalus increase phagocytosis (the engulfing of microorganism invaders by the immune system), increase production of immunoglobulins and macrophages and modulate the pituitary-adrenal cortical activity. Astragalus protects the kidneys and lungs from damage from autoantibody complexes, regulates sweating, decreases fatigue and increases tolerance to stress.
Astragalus protects against oxidative damage by increasing mitochondrial function without increasing the mitochondrial oxygen consumption. In the liver, astragalus is a mild choleretic and also increases repairs in chronic viral hepatitis while reducing inflammation and othersymptoms. Astragalus also lengthens telomeres for longevity(TA 65 is a very pricey extract made from Astragalus that is touted to reduce all the effects of aging and mimics pretty much all the benefits of the inexpensive herb form of astragalus). Astragalus even increases motility of human sperm.
Astragalus is considered to be a cardiac tonic.In the cardiovascular system, the saponins in astragalus inhibit lipid peroxidation in the myocardium and one study using patients with angina revealed that cardiac output increased after two weeks of treatment. Astragalus strengthens left ventricular function and reduces free radical damage in patients after a heart attack and increases super oxide dismutase activity in cardiac muscle.
Astragalus: the unsung cancer fighter
Studies at the University of Houston have shown that astragalus can improve immune function in cancer patients by increasing T-cell counts. Astragalus increases the ability of NK cells and T-cells to kill cancer cells while switching on the anti-tumor activity of Interleukin-2. Inchemotherapy treatmentsastragalus provides anti-neoplastic activity anddecreasesimmunosupression. Astragalus reduces the consequences with both chemo and radiation of fatigue,weight loss, anemia, nausea and loss of strength while increasing WBC production for leucopenia (a common side effect of immunosuppressive therapy), thereby decreasing life-threatening infections.
Even though this incredible herb is listed on the Botanical Herbs Board Exams and in theCompendium of Pharmacological Actions of Medicinal Plants and Their Constituents, naming the benefits of astragalus can bring a warning letter from both the FDA and FTC, as Dr. Andrew Weil found out when he listed the benefits of taking astragalus to prevent the swine flu. So don’t expect to see any of this information on a vitamin or herb label. Despite what modern medicine and the FDA says, healing did occur long before pharmaceuticals were invented. True health comes by good foods, minerals, herbs, fasting and cleansing. Astragalus is a good guy for natural health!
Sources:
Compendium of Pharmacological Actions of Medicinal Plants and Their Constituents, Compiled and copyrighted by Eric Yarnell, ND Actions of Medicinal Plants 2007 Eric Yarnell, ND
Zhang CZ, Wang SX, Zhang Y, Chen JP, Liang XM. “In vitro estrogenic activities of Chinese medicinal plants traditionally used for the management of menopausal symptoms.” J Ethnopharmacol 2005;98(3):295-300.
Nutrition 740 notes Spring 2006, Dr. Mona Morstein, SCNM
About the author:
Craig Stellpflug is a Cancer Nutrition Specialist, Lifestyle Coach and Neuro Development Consultant at Healing Pathways Medical Clinic, Scottsdale, AZ. With 17 years of clinical experience working with both brain disorders and cancer, Craig has seen first-hand the devastating effects of vaccines and pharmaceuticals on the human body and has come to the conclusion that a natural lifestyle and natural remedies are the true answers to health and vibrant living. You can find his daily health blog atwww.blog.realhealthtalk.comand his articles and radio show archives atwww.realhealthtalk.com
For the last few days the Health Care Bill has been being debated before the Supreme Court, what the main stream media has not talked about Micro chip tracking a national medical device registry of all American People. If the Health Care passes it will be mandatory by March 28th 2013! Can you say Mark of the beast system being set up 666?
Correction of the facts: Credit belongs to Ed Darrell for pointing out our mistake thanks again Ed Darrell for keeping us on the Straight and narrow and on point with truth! Mark of the Beast 666 Micro chipping of all the American People if the Health Care passes a (((National Medical Device Registry))) will be mandatory by March 28th 2013!
OK Ed Darrell as to your question about the health care bill and the chip being mandatory. You are correct it will not be mandatory for people to have it implanted at this point in time. ” If the Health Care passes it will be mandatory by March 28th 2013! Can you say Mark of the beast system being set up 666?” Daniel J Leach OK Yes the Health care bill does make a system for tracking Micro chip’s in a national medical device registry for all American People MANDATORY
A teacher of law, economics, history, AP government, psychology and science. Former speechwriter, press guy and legislative aide in U.S. Senate. Former Department of Education. My blog, Millard Fillmore’s Bathtub, is a continuing experiment to test how to use blogs to improve and speed up learning processes for students, perhaps by making some of the courses actually interesting. It is a blog for teachers, to see if we can use blogs. It is for people interested in social studies and social studies education, to see if we can learn to get it right. It’s a blog for science fans, to promote good science and good science policy. It’s a blog for people interested in good government and how to achieve it.
The company that manufactured medical information RFID chips stopped in 2010. No market. There is no company making such chips now, so were there a provision in the law, it could not be met.
So would you like to go and buy some chips and how many? Embedded Solutions » Engineering Tools » RF / Wireless Development Tools » RFID Transponder’s. So tell me again Mr
Ed Darrell how that no company’s making or stopped making the chips and technologies or tools for the RFID chips. Sorry government troll you lose this battle. People just do a Google search on the subject and you will find lots of chips. http://www.mouser.com/Search/Refine.aspx?cm_mmc=google-_-ppc-_-americas-_-EmbeddedSolutions&gclid=CJ7umc7hzrMCFUOK4AodhBoATg&N=15148064
I did a search for “Sub Title C-11 Sec:2521” on Google, and found many posts essentially saying the same thing. I also found the text of both the House bill and the Senate bill, and there is no “Sub Title C-11 Sec:2521.”
There is, however, a section on a national medical device registry (Sub Title C, Section 2561), which reads: “The Secretary shall establish a national medical device registry (in this subsection referred to as the ‘registry’) to facilitate analysis of postmarket safety and outcomes data on each device that (a) is or has been used in or on a patient; and (b) is…a device that is implantable, life supporting or life-sustaining.”
So basically, the bill put forth by the U.S. House of Representatives wants to track the results of these devices and link them to a registry so a doctor looking to implant a device in a patient can check whether it actually worked in previous patients who received the device. There is no mention of RFID, and no mention of tracking individuals who receive the device.
Mark Roberti is the founder and editor of RFID Journal. If you would like to comment on this article, click on the link below. To read more of Mark’s opinions, visit the RFID Journal Blog or click here
“Buried deep within the over 1,000 pages of the massive US Health Care Bill (PDF) in a “non-discussed” section titled: Subtitle C-11 Sec. 2521— National Medical Device Registry, and which states its purpose as:
“The Secretary shall establish a national medical device registry (in this subsection referred to as the ‘registry’) to facilitate analysis of postmarket safety and outcomes data on each device that—‘‘(A) is or has been used in or on a patient; and ‘‘(B) is a class III device; or ‘‘(ii) a class II device that is implantable.”
In “real world speak”, according to this report, this new law, when fully implemented, provides the framework for making the United States the first Nation in the World to require each and every one of its citizens to have implanted in them a radio-frequency identification (RFID) microchip for the purpose of controlling who is, or isn’t, allowed medical care in their country.
Can we say that Satan has found a new way to keep track of Gods people?
I think so.
Revelation 13
1And I stood upon the sand of the sea, and saw a beast rise up out of the sea, having seven heads and ten horns, and upon his horns ten crowns, and upon his heads the name of blasphemy.
2And the beast which I saw was like unto a leopard, and his feet were as the feet of a bear, and his mouth as the mouth of a lion: and the dragon gave him his power, and his seat, and great authority.
3And I saw one of his heads as it were wounded to death; and his deadly wound was healed: and all the world wondered after the beast.
4And they worshipped the dragon which gave power unto the beast: and they worshipped the beast, saying, Who is like unto the beast? who is able to make war with him?
5And there was given unto him a mouth speaking great things and blasphemies; and power was given unto him to continue forty and two months.
6And he opened his mouth in blasphemy against God, to blaspheme his name, and his tabernacle, and them that dwell in heaven.
7And it was given unto him to make war with the saints, and to overcome them: and power was given him over all kindreds, and tongues, and nations.
8And all that dwell upon the earth shall worship him, whose names are not written in the book of life of the Lamb slain from the foundation of the world.
9If any man have an ear, let him hear.
10He that leadeth into captivity shall go into captivity: he that killeth with the sword must be killed with the sword. Here is the patience and the faith of the saints.
11And I beheld another beast coming up out of the earth; and he had two horns like a lamb, and he spake as a dragon.
12And he exerciseth all the power of the first beast before him, and causeth the earth and them which dwell therein to worship the first beast, whose deadly wound was healed.
13And he doeth great wonders, so that he maketh fire come down from heaven on the earth in the sight of men,
14And deceiveth them that dwell on the earth by the means of those miracles which he had power to do in the sight of the beast; saying to them that dwell on the earth, that they should make an image to the beast, which had the wound by a sword, and did live.
15And he had power to give life unto the image of the beast, that the image of the beast should both speak, and cause that as many as would not worship the image of the beast should be killed.
16And he causeth all, both small and great, rich and poor, free and bond, to receive a mark in their right hand, or in their foreheads:
17And that no man might buy or sell, save he that had the mark, or the name of the beast, or the number of his name.
18Here is wisdom. Let him that hath understanding count the number of the beast: for it is the number of a man; and his number is Six hundred threescore and six. This = 666
Yes Ill say it! Cancer Cures that the NWO Government doesn’t want you to know about! We all know of someone who has had cancer or has died of cancer. Wouldn’t it be great if Cancer was not a death sentence but instead it was just like the common cold. Some people believe that to be the case. I myself am a believer in the Great Cancer Cover up.
This is why! When I was a younger man in my early twenty’s I was part of a live AM Radio Broadcast show. Myself and a bunch of Anti NWO Patriots from the Rochester NY area started a live Radio show Thursday nights at 7pm broadcast from 1310 AM WASB a small Radio Station that ran Programs out of Brockport NY http://sonshinenetwork.com/ While doing a broadcast I had the opportunity to listen in on a life changing conversation with Charles Pixley http://www.whale.to/m/pixley.html
Charles Pixley and 714x
Charles Pixley was convicted in Rochester NY and released from a federal prison outside of Harrisburg, Pennsylvania.
The Charles Pixley Story is about a man who was using Natural Cures for Cancer treatment and was sent to prison for using 714x inside the United States of America. Charles Pixley was not convicted for killing people with 714x but for transporting it across the USA border from Canada. I personally had a chance to ask Charles Pixley many questions about his practice and what he was doing with 714x and how it worked to cure people of cancer. This is what Charles Pixley had to say!
“Dear Beloved of the Eternal:
Let me start by saying: “You cannot poison a sick person well.”
The war on cancer is like any other, it has its casualties and its cause.
Its casualties are the same as any other war, those who are meek and those who fight against the tyranny which perpetuates it.
Its cause is also the same; money and ignorance.
It always saddens me to the marrow to hear the horror story of each and every therapeutic failure posing as legitimate therapies,
which are protected by the Pharma Cartel through the auspices of the FDA and various other agencies they employ to apply pressure and force suppression through insurmountable pressures.
If chemo-therapy and radiation has been a known failure for 50 years, so what makes anyone think it ever will work?
Over 50,000,000 Americans have succumbed to this form of brutal perfected form of genocide and tyranny over the last 20 years alone.
It comes with a hefty price tag costing the taxpayer or insurance premium payee around $4 TRILLION dollars per year.
These funds are pour unabated into the hands of the Pharma/AMA/HMO medical cartels.
What matters is what you want and what your heart tells you make your own decisions, based upon Knowledge not pressure of allopathic mortality charts, the game is fixed!
Are you in touch with our Creator?
The Body, Mind and Spirit are not separate things. They are all part of the divine creation of the Faculty of THE IMMORTAL Mental Being.
The damage done by chemo and radiation has the potential of being reversed. Life is easily restorable, because it is born of HIS Divine Knowledge and are VIBRATIONS OF LIGHT, remember and tap into IT!!!
Dis-Ease is lack of Ease.
Therapeutic successes come about with a combination of prayer, Will, letting go of the fear and embracing LOVE, determination, commitment, elimination of toxic overload, physical immune enhancing enzymes, change in diet, change in attitude and cleansing the mind uprooting the cancerous thought processes, oxygenation and exercise.
Unfortunately and potentially fortunately there is the distinct possibility you never HAD cancer to begin with.
The testing methods used are not very accurate industry wide they have a 40% to 70% false positive/negative rate.
What can you do if you need medical consultation?
Suggest reading the following introductory letter and press release and then call for a consultation. There is a fee: Dietmar Schildwaechter, Ph.D.., MD, 703 430 7789
Dr. Schildwaechter is a Paracelcius Award winning Laureate and one of the most brilliant world leading oncologists. Has crossed the abyss from orthodox to “holistic,” has a clinic in Germany and is most capable of helping you out of this maze.
ALL are ignorant of the Absolute Knowledge and Power of the ONE and ONLY healer in Truth and Faith call upon Him now! In the name of the HOLY ABSOLUTE ONE, remember and be healed. This now manifests, AMEN!
As a nation, we are synthesizing the realities of genuine health care, scientific blindness, socio-political force and restraint disguised as health care reform. In my view we have arrived at the dawning of an evolutionary cycle and energy medicine is the future of medicine here and worldwide.
Our great medical colleges are being forced by consumer demands to return to their foundational roots of traditional medicine. The legal facade is crumbling see enclosure and “unscientific” accusation is dead.
On March 15 it was revealed: “Thanks to research by California Institute of Technology chemistry professor Shui Yin Lo, who was performing experiments on how to improve car engine efficiency. Lo found that water molecules, which are random in their normal state, begin to form a cluster when a substance is added to water and the water is vigorously shaken — the exact process homeopaths use to create their medicine. Lo said every substance exerts its own unique influence on the water, so each cluster shape and configuration is unique to the substance added. With each dilution and shaking, the clusters grow bigger and stronger. This water, which homeopaths call “potentized,” is considered “structured water,” because the water molecules have taken on a shape influenced by the original substance. Wired News: “Homeopathy — Dilute And Heal” by Andy Patrizio.
Present day systemic tedium of illusory falsehood creating division, disease maintenance, destruction and death are relegated to the past. Mass exodus from allopathic failure is in progress.
Knowledge is indivisible and ONE. Re-membering the branches of knowledge, our birth Right of health, happiness and life extension defines the natural paradigm.
How can you help me?
A protagonist by nature I have the spiritual commitment, vision, experience, enthusiasm, and contacts to assist. I am prepared to define, educate, guide, perform, promote and redirect cash flow to accelerate change.
Hard cash savings accrued on the corporate balance sheets and human resource benefits will far out weigh and thus enable the enormous profits this creative endeavor will yield.
I am grateful for any type of assistance, or referral to a potential employer.Peace, ”
Charles Pixley
National Executive Director,
Association of Eclectic Physicians
(716) 544 2288
Charles Pixley was recently released from a federal prison camp outside of Harrisburg, Pennsylvania. His crime? He had made available to the American public knowledge of and access to 714X, a homeopathic camphor compound which is available to the Canadian public and is regarded as a highly successful therapy against cancer. After a lengthy court battle, which left him financially ruined, Pixley was sentenced to nineteen years in federal prison.
Even though he is a medical layman, Pixley’s story is similar to that of other scientists and physicians who sought to defeat disease outside the accepted conventions of orthodox medicine. The faces and names change, but the story is the same. A physician, scientist or researcher seeks to develop or make available a treatment for cancer or some other deadly disease. These are sought out by patients who are in the advanced stages of their disease, whose bank accounts have been drained by the medical establishment, and who despair of finding a cure in those realms. As alternatives to the established therapies are presented to them, the U.S. Food and Drug Administration (FDA) sweeps in, seizing research materials, patient lists and all assets in a fit of Gestapo-like fury. Professional and financial ruin and sometimes incarceration are all that is left for those who make treatment alternatives available to the ill.
This was the experience of Charles Pixley. In 1989 microbiologist Gaston Naessens was acquitted of charges in Canada that he contributed to the death of a terminal cancer patient he had introduced to 714X. After that momentous three-year court battle, Naessens’ camphor-based compound was made available for legal prescription by the Canadian Department of Health and Welfare. According to Pixley, it has since been used with varying but significant degrees of success by over 100,000 terminal cancer patients without one instance of side effect. It is also inexpensive.
THE STORY BEGINS
In 1990 Pixley, his wife and an associate started Writers and Research, Inc. in Rochester, N.Y. for the purpose of promoting specific works they considered to be of immediate and practical benefit to the public in regards to the fields of business, environment, health and socio-politics. As they began to study the fields of health and medicine they were excited to learn that successful therapies for cancer actually existed, but were being withheld from the public. They then formed the Institutional Review Board (IRB) for the exclusive promotion of the research and discoveries of Gaston Naessens and 714X, the homeopathic compound he formulated.
Pixley told The WINDS, “One-hundred percent of the people we were working with were final stage terminal according to the standard oncologist. They had already completed their chemotherapy and radiation and now were in a state where there was no more money for them. They were at death’s door as a result of the [orthodox] therapy.”
Pixley states that from the inception of the IRB in April of 1992, they were visited regularly by the FDA who “requested and received copies of all available research, toxicology studies, spectrographic chemical evaluations, rat studies, patient histories, books, tapes, and samples of the 714X.” Even though they cooperated fully with the FDA, in 1995 their office was raided. Computers, books, tapes, business records and patients’ personal medical records were seized.
After several attempts, the U.S. Attorney succeeded in having a Grand Jury indict him and his corporation as co-conspirators for “conspiring to defraud the United States by importation of an unapproved new drug,” a felony under Title 18 U.S.C. 321. Pixley later determined through the Freedom of Information Act that this FDA regulation had never been published in the Federal Register and, therefore, was not promulgated according to the law. This did not seem to matter. Pixley was ordered into Federal Court in April of 1996.
As a defense Pixley planned to expose the evident policy of the FDA to suppress life-saving therapies, both to protect the profits of the medical/pharmaceutical cartels and to carry out a larger agenda of population reduction. The prosecution “filed a ‘motion in limine’, which was designed to prevent me from saying anything or putting up any defense whatsoever,” Pixley told The WINDS. “Even though they didn’t know what my defense was going to be, they had an inkling that I was going to start accusing the government of genocide” before the jury. “Their goal was to put me away no matter what.” Pixley was found guilty and sentenced to nineteen years in prison. His sentence was later reduced on appeal to a year and a month, partly, he feels, because he was allowed to present arguments detailing the government’s suppression of non-orthodox therapies.
During his interview with The WINDS, Pixley did not dwell on his trial and imprisonment or even his financial devastation and lifetime status of “convicted felon.” He speaks and writes mainly of the medical monopoly and its protectors at the FDA, as well as the thousands of cancer patients that are denied alternatives. “In my view,” he writes, “the ones who are being punished are the American people who are denied access to life-saving therapies.”
THE MEDICINE WAR
Pixley states that until early this century homeopathy, eclectic medicine and native herbalism (naturopathic medicine) were the dominant therapies in the United States. Up to 65 percent of the population received treatments from these sources. Homeopathic medicine is perhaps the best known of these alternatives today. Homeopathy, which essentially supports the body’s natural healing processes, was developed by Dr. Christian Friedrich Samuel Hahnemann in the late 1750’s. This doctor also coined the term “allopathy”, which describes the established orthodox medicine today.
According to Pixley, allopathy focuses on disease as an external invader to be attacked with drugs, radiation and invasive procedures. The disease is the focus rather than the imbalances in the patient’s body. Allopathic prescription drugs are developed from active agents found in animals or plants (recognized by homeopaths as beneficial in their natural state), extracted from their natural source, and then synthesized and chemically altered to increase potency. In their unnatural state these drugs become poisonous, producing “side effects” and weakening the body’s natural healing mechanisms. Naessens’ 714X is formulated to bolster the body’s defenses as opposed to conventional drugs, radiation and chemotherapy which weaken them.
Pixley told The WINDS that in the early 20’s the giant Rockefeller trust took over the American Medical Association (AMA) which then issued a report attacking homeopathic medicine. The AMA, along with insurance and pharmaceutical companies, promoted allopathic medicine because its scientific nature is easier to dominate and profit from. Medical insurance became exclusively devoted to allopathy and political lobbies brought government support. Over time the alternatives lost significant income and public recognition.
The resulting monolith that has evolved during the rest of this century astounds Pixley and others like him. The FDA, an agency with federal police powers, is dominated by the massive allopathic drug and medical complex which uses those police powers to enforce their orthodoxy on the rest of the country. Said Pixley, “Regarding the FDA, you’re dealing with an agency that is out of control. You’re dealing with a paradigm mentality. You’re dealing with billions and billions of dollars that are sunk into the research mill. You’re dealing with companies that take the results of their drug testing — phase one, phase two and phase three trials — to the FDA, and the panels that review that paperwork are chaired by members of the board [of the submitting drug companies]. The official at the FDA many times is from the [drug] company, who is now at the FDA, so there is a revolving door policy.”
LEGAL QUACKERY AND THE POISON CURE
Since President Nixon declared “war on cancer” in 1971, the United States has spent tens of billions of taxpayer dollars on cancer research, and is it any wonder that some people have become outraged at allopathy’s abysmal failure to find a cure? After twenty-seven years the only treatments offered are radiation, chemotherapy and surgery, two which are cancer causing and all of which are devastating to the body’s efforts to heal itself. The long-standing survival rate of cancer patients using orthodox therapies remains at 3%, yet, efforts to find alternatives still excite the rage of the FDA Gestapo.
The abysmal failure of cancer research may be found in the amount of money spent on cancer. Pixley quotes Health United States, a government publication which reports that 2,500,000 people in the U.S. die every year from cancer, a number that is on the rise. Another writer claims that the number of people dying from cancer every year is exceeded by those making a comfortable living, mostly at taxpayer expense, in the cancer research industry.
In addition to the pain, suffering and loss of productivity inflicted by each case of cancer, there is also a lot of money involved. Considering that treatment costs $80,000 to $160,000 per person over the past twenty years, the cost adds up to $200,000,000 to $370,000,000 per year and 50,000,000 lives, or a total of $4 trillion to $7.5 trillion. The entire medical industry represents one-seventh of the total American GNP at one trillion dollars per year with revenues for all parties involved with cancer at $400 billion annually.
Pixley pointed out that allopathy accuses healing alternatives such as homeopathy of offering a false hope to cancer patients, but all allopathy offers is the same old radiation, chemo and surgery treatments that produce the same dismal results. If a drug produced by a major drug company causes death or major side effects (this has happened many times), you will never see a company officer, research assistant or testing lab subjected to a raid, indictment or jail term. This treatment is reserved for the competition which may offer a much better therapy but threatens the profits of the cancer industry.
THE QUESTION OF MOTIVATION
“Informed consent” laws require physicians to advise their patients of the available therapies so they may make an informed choice. Without a doubt, there is a conspiracy to exclude non-allopathic therapies from the selection. Like many other diseases, cancer is too profitable for a cure to be permitted. Arms manufacturers in the United States increase their wealth and power by influencing a policy of war in the name of peace. It seems evident that the “war on drugs” is perpetuated not to eliminate the drug problem, but to enhance the prison industrial complex, steal private property and incarcerate and enslave the surplus population.
It appears that the drug/medical aegis pursues the same cynical course in the “war on cancer”, the apparent goal not being a cure or effective treatment but a perpetuation of disease for profit. It has been alleged that the social policy of the brave new world order requires a reduction of population. The tremendous volume of wealth flowing into the medical/pharmaceutical research cartel has created a massive health care complex that possesses, like some great beast, a keen instinct for survival. Both social policy and hunger for corporate profit have combined to create a system that loots the public, either directly or through tax subsidy, and often creates a “final solution” as its final product.
With a sense of irony, Pixley noted that synchronously to the day of his trial the Second and Ninth Circuit Courts of Appeal ruled that “doctor assisted suicide” is within our constitutional right. As this story was bring prepared, Paul Harvey announced that a study published in the New England Journal of Medicine last April reports that six percent of physicians surveyed assisted patients in committing suicide, either in administering a lethal injection or in writing a prescription that would do it. (Paul Harvey, ABC News, 8-12-98). The trends in medically-induced death are accelerating at an astonishing pace.
The FDA and the pharmaceutical funded “anti-quackery” groups claim to be protecting the public from charlatans and snake oil salesmen. While it may seem reasonable to do this, what the government has really done is remove all freedom from the individual to study the alternatives and then choose the therapy he/she deems best for his/her own body. Both information and access to alternatives are blocked by the police powers of the FDA, leaving most people the choice between allopathic medicine or traveling abroad for treatment.
While it is true there are alternatives that may not be effective and even harmful, and that “snake oil salesmen” undoubtedly exist, no real or alleged threat justifies removing the freedom of the individual to choose for him/herself, putting everyone’s health under the control of a group of self-appointed medical oligarchs. This group of profit-mongers are the real snake oil salesmen.
WHAT IS 714X ?
Pixley stated that 714X is not a panacea. It is merely a part of a “holistic therapy” which may include “specific proteolytic enzymes with a detoxifying diet, vitamin-mineral supplements and a strict avoidance of deadly therapies.” He emphasizes that people cannot be standardized and must inform themselves as to what is best for them.
Even though many patients who turned to 714X were in the terminal stages of cancer, there were a significant number who experienced reversals in their disease. “At that stage the conservative estimate is twelve percent long-term survival, but realistically it’s more like fifty percent,” Pixley said.
Near the end of his interview with The WINDS Pixley gave a definitive overview of FDA policy. He said:
“Here is something [714X] that is proven and known for twenty years to reverse cancer. Sometimes terminal cancer is eliminated in ninety days. Rather than showing me how to get this approved [by the FDA] because it is such a wonderful thing, they make it so difficult. They first threaten you. If you don’t obey, they send the FDA police and then if you don’t comply, they indict you.
“The FDA should be proactive. If there is a cure, they should do everything in their power to make sure the American public has it. When the FDA covers it up or blocks it, that’s genocide.”
In addition to interviewing Pixley, The WINDS staff referred to the following source material for this story:
1. YOGA FOR THE 21st CENTURY, an article by Charles Pixley, 6-21-98.
2. An open letter by Charles Pixley reviewing standard medical practices and the alternatives.
3. An open letter from William H. Moore [Pixley’s attorney] to Congressman Jack Kingston, 3-22-95.
Written 08/17/98
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