AN OVERVIEW ON THE POLIO VACCINE
by Mary Tocco
January 27, 2008
I get asked regularly about the polio epidemic in the 1900’s and those who ask me feel that the vaccine is responsible for saving thousands of lives. They also believe the vaccine eradicated polio. I share this with you to hopefully give those who grew up in the 1920’s to 1950’s a different point of view. Often, they recall someone who was struck with polio or other infectious illnesses that would leave them paralyzed or permanently ill. Yes, it is true that many were unfortunate and suffered with paralysis but we must not assume that because polio is no longer a threat in this country that the vaccine is the reason for this decline. Let me addresses this topic from a historical view.
First, looking back historically, these infectious illnesses referred to were very prevalent in the mid 1800’s to early 1900’s. Several studies have proven that these infectious diseases were almost completely gone before vaccines were introduced. The death rates were at all time lows through out United States, Great Brittan and countries without vaccines also had decreases. I believe that Americans have been sold a lie. The following quote is from a very reliable source and is one of many that document that death from infectious illnesses was at an all time low before vaccines were introduced.
“According to the World Health Statistics Annual of 1973-1976 said that there had been a steady decline in infectious diseases in most developing countries regardless of vaccines administered. They believe that the diseases disappeared as a result of improved sanitation, improved water supplies improved personal hygiene and better nutrition. In addition, diseases for which there were no vaccines also declined dramatically. From 1850 to 1940, diseases had declined by 90% and were at an all time low, just when vaccines were being introduced.”
Imagine living in the turn of the century where we lived with animals and their by- products, used their fur and feathers in our homes, no refrigeration, no running water, poor food storage infected with rodents and bugs, poor personal hygiene, shallow wells near out houses, ponds and rivers for washing our bodies shared by animals…. It was not a clean environment. As we began to improve all of these things including waste water treatment and sewer systems, better nutrition and clean drinking water, illnesses and death from infectious illness decreased dramatically. Another great study that comes up with the same conclusion, Medical Measures and the Decline of Mortality by , St. Martin’s Press, New York states “It is estimated that at most, 3.5% of the total decline in mortality since 1900 could be ascribed to medical measures introduced for the diseases considered.” Furthermore, medical measures were introduced several decades after marked decline had already set in and having no detectable influences in most instances.”
The American Medical Association and the Center for Disease Control have taken credit for eradicating diseases in the United States when in fact; they were on their way out because of previously stated reasons. Small pox is often referred to as the “great success story” and yet the vaccine had very little to do with eradication. Only 10% of the world’s population received the vaccine. In a June 19-20, 2002 meeting in Atlanta Georgia after 911 when the government was debating to bring back the small pox vaccine, the Advisory Committee on Immunizations Practice said, “Small pox would have died out on its own due to improved sanitation, improved water supply and improved nutrition.”
I have been researching the “risks of vaccinations” for the last 27 years. What I have learned about the polio vaccines used in this country is not only shocking but will affect millions. Consider these facts:
It is known that the live polio vaccine contained SV40, a cancer-producing virus and for the first time a hearing was held in Washington on September 9, 2003 by the Subcommittee on Human Health and Wellness, U.S. Government Reform Committee Chaired by Congressman Burton (R-IN). SV40 is associated with brain, bone and lung tumors found in children and adults today from vaccinations. This vaccine was used until the late 90’s.
Previously in Washington on August 3, 1999 at a Polio Vaccine Hearing by the Committee on Government Reform and Oversight and House of Representatives, the following testimony was not reported in the evening news! I have met Dr. Howard Urnovitz on several occasions when he has presented the results of his research. He has dedicated his life to cancer research and vaccines. Here is a portion of his written testimony: “I am grateful to this committee for allowing me to address the issue of vaccine safety. I am Dr. Howard B. Urnovitz. In 1979, I received my doctorate degree in Microbiology and Immunology from the University of Michigan, where I studied vaccines. I am testifying today as the Scientific Director of the Chronic Illness Research Foundation. For the record, I am also the chief science officer of a biotechnology corporation. On the issue of informed consent: Had my mother and father known that the polio virus vaccines of the 1950s were heavily contaminated with more than 26 monkey viruses, including the cancer virus SV40, I can say with certainty that they would not have allowed their children and themselves to take those vaccines. Both of my parents might not have developed cancers suspected of being vaccine-related, and might even be alive today. Government, industry, and medicine should embrace the ethical principle of informed consent about possible adverse reactions associated with vaccines.”
Our government is trying to hide behind “junk science” riddled with conflict of interest. Our Institute of Medicine, Federal Drug Administration and the Center for Disease Control all refuse to acknowledge the injuries caused by vaccination. The time is coming when they will not be able to deny their responsibility in the catastrophic rise in illness due to toxic vaccines. Thank God, we stopped using the live polio virus vaccine in the late 1990’s because it was the cause of almost all of the polio in this country since the 1980’s when they began to track it.
How did we get so programmed? Could it be that a whole generation of Americans has been told a big lie? The reality is that we are the victims of very carefully planned out conditioning that has been going on for many years. According to Dr. Robert Mendelsohn, renowned pediatrician for 30 years and author of several books such as, “The Medical Heretic” and “How to Raise a Healthy Child in Spite of Your Doctor, he writes the following; “The pediatrician serves as the recruiter for the medical profession. He indoctrinates your child from birth into a lifelong dependency on medical intervention. The best way to raise a healthy child is to keep him/her away from the doctors except emergency care. Most doctors ignore the fact that the human body is a wondrous machine with the astonishing capacity to repair itself.” Dr. Mendelsohn goes on to say, “The first stage of the indoctrination is the well baby visit- a cherished ritual of the pediatrician that enhances their income but does nothing constructive for your child. Well baby visits are worthless…” page 24-24. “The purpose of the pediatrician is to vaccinate your child.” In chapter 19 he states, “The greatest threat of childhood disease lies in the dangerous and ineffectual efforts made to prevent them-mass immunizations.” He goes on to call vaccines the “sacred cow” of modern medicine.
Most parents do not know what they are consenting to, just as I believe most doctors who promote vaccines do not know what they were injecting when they vaccinate. After attending my vaccine presentations, most parents will think hard and long before giving any vaccines and most importantly, will make a fully informed decision, understanding all the risks.
I believe in Freedom and Liberty. As a parent, an American and an adult, I do not want my government telling me what I must put into my body or my children’s bodies. I no longer trust those who hold powerful positions in our government because I believe their motive is no longer the well being of the citizens of this country. Vaccines, at this time, are the only mandated drugs and therefore, should be proven safe and effective. There are no long term safety studies and the studies the drug manufactures present are flawed and bias. The Institute of Medicine gets a percent of every vaccine given in this country. There should be no financial ties allowed.
I love this quote!
“When we give the power to government to make medical decisions for us, in essence, the state owns our bodies.”
Dr. Ron Paul M.D. U.S. Representative, 2008 Republican nominee for president.
Parents, it is up to you to make this very important decision. Take the time necessary to investigate all the childhood recommended vaccines before you sign a consent form. We do not live with the same threat of illness as the generations before us did. We have many options other than vaccination that do not carry the level of risk. Because of vaccines, we now have a whole generation of children who suffer with chronic, life long health issues. I believe there is a happy balance where we are active in promoting health. My opinion is that when a healthy child gets normal childhood illnesses, it will help that child develop a strong immune system. Nothing in the body gets strengthened by avoidance, only by over coming challenges.
I have spent thousands of hours investigating the facts and now you can benefit from my 27 years of work. My three hour fully documented DVD; “Are Vaccines Safe?” is now available.
I appreciate your emails and your opinions are welcome.
© 2008 – Mary Tocco – All Rights Reserved
E-Mails are used strictly for NWVs alerts, not for sale
Mary Tocco is currently managing/owner of Vitalityhealth LLC, in Charleston, SC and I work with my daughter, Dr. Renee Tocco, who is a chiropractor and the clinic director. I have been working in the chiropractic field since April of 1981. I have organized workshops outside the office on health topics and have been public speaking on health issues for the last thirteen years. I attend yearly vaccine conferences sponsored by the state of Michigan as well as other conferences on issues pertaining to vaccines.
Mary’s studies have included natural cooking, natural birthing, home births, breast-feeding. I have had four home births and have successfully raised our five children outside the medical model utilizing a vitalistic healthcare approach (no drugs or surgeries). I have researched vaccines/immunizations for the last twenty-seven years and in August of 2006; I released my DVD called, “Are Vaccines Safe?”
Flame Retardants: Dangerous chemical now in breast milk
06 December 2007
Flame retardant chemicals, which are in household furniture, textiles and electronic equipment, have found their way into human breast milk. Scientists aren’t sure how this may affect the developing child, but it’s feared it may cause neurological problems and disrupt thyroid function.
One study has found that the level of the retardant PBDE (polybrominated diphenyl ethers) has increased 200 times in breast milk in women in North America, while another study in Sweden has discovered the level has increased 60 times in a span of 25 years.
PBDEs have regularly been included in a range of household and office items since the 1970s, but scientists have only recently discovered just how dangerous the chemical can be. Regulators across Europe and the US have banned some elements of the chemical, and the brominated mix will be removed under new legislation that comes into force in 2008.
But items of furniture and furnishings that contain the original compound are still in millions of homes. Unlike other pollutants such as PCBs and DDT, the PBDEs particularly affect infants. Scientists have found a direct link between breast milk and household dust, and they estimate that toddlers’ exposure to PBDEs from household dust is 100 times greater than that for adults because of breast milk and more hand-to-mouth contact.
(Source: The Lancet, 2007; 370: 1813-4)
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Detoxification – for Your Health
Stimulating your detoxification systems can be done through a number of nutrients.
phase 1 Stimulation
· Thngeretin (from tangerines)
· Riboflavin and carotenoids (such as beta-carotene, alpha-carotene, lycopene, lutein, and astaxanthin)
Phase 1 stimulation can render some chemicals toxic – the following nutrients protect against this toxicity.
phase 1 Inhibition
· Hesperidin (oranges)
· Naringenin (grapefruit)
· Resveratrol (grape skins)
· Quercetin (onions, teas, apples, and most vegetables)
· Apigenin (celery, parsley, and ginkgo biloba)
· Ferulic acid (fruits)
· Chlorogenic acid (Mackintosh apples, blueberries, eggplant)
phase 2 Stimulation
· Indole-3-carbinol (broccoli, Brussels sprouts and other cruciferous vegetables)
· Isothiocyanates and sulforaphane (broccoli and Brussels sprouts)
· Thurine (an amino acid – available as a supplement)
· Glutathione (supplied by N-acetyl L-cysteine, ellagic acid and alpha-lipoic acid – all
available as supplements)
· Glycine (an amino acid supplement – high intakes can cause excitotoxicity)
· MSM (methylsulfonylmethane – a supplement)
· Quercetin (teas, onions, cranberries, and most vegetables)
Stinlulation for Both Phase 1 and phase 2
· Curcumin (from the spice turmeric, also a supplement)
· Astaxanthin and canthaxanthin (from all vegetables and fruits and also available as a supplement called mixed carotenoids
Six Additional Supplements That Improve Liver Health
Your liver plays a crucial role in your overall health. Here are nutrients that focus on protecting the liver.
· Lecithin (phosphatidylcholine)
· Curcumin also protects the liver from free radical damage and improves bile flow
· Alpha-lipoic acid has been shown to protect the liver from some extremely powerful toxins and from hepatitis C and A damage.
· Silymarin (extracted from the milk thistle plant) protects the liver and brain and stimulates liver regeneration.
· Vitamin C (as magnesium ascorbate) protects the liver from free radical damage
· Magnesium protects the liver from free radicals and inflammation and increases glutathione levels
THE LIVER AND DETOXIFICATION
The liver keeps us clean on the inside and prevents dangerous chemicals from penetrating their way deeper into our bodies. The liver is the gateway to the body and in this day and age has an enormous workload that frequently overloads its detoxification systems. The liver must cope with every toxic chemical in our food chain as well as excessive amounts of unhealthy fats and animal protein that are ubiquitous in fast foods. Let us examine in more detail the mechanisms by which the liver keeps our internal body clean.
THE LIVER FILTER
If we examine the liver under a microscope we see rows of liver cells separated by spaces called sinusoids. Sinusoids are structured like a filter or sieve through which the blood stream is filtered. During this process the filter removes unwanted particulate matter, microorganisms and metabolic waste products. These noxious thing are ingested by specialized cells in the sinusoids called “Kupffer cells” which break down and destroy these things, rendering them harmless. The sinusoids and Kuffer cells are like a “garbage disposal unit” inside the liver. Thus you can see that the liver is the filter and cleanses the blood stream which is of vital importance.
Inside the liver cells (hepatocytes) we find sophisticated enzyme pathways or chemical pathways that have evolved over millions of years, to breakdown toxic substances. Every drug, artificial chemical, pesticide and hormone is broken down or metabolized by these pathways inside the liver cells. Basically there are two major detoxification pathways inside the liver cells which are called the Phase One and Phase Two pathways.
This is called the cytochrome P450 enzyme system where a liver cell takes a toxic chemical and through a process of oxidation, reduction, hydrolysis or hydroxylation turns it into a less harmful substance. During this process oxygen free radicals are generated, so there is a need for antioxidants, especially Vitamin C, to prevent cellular damage. For efficient phase one detoxification to occur the liver requires adequate amounts of the nutrients selenium, folic acid, vitamins B2, B3, B6, phophatidyl choline and bioflavonoids. If these nutrients are lacking, toxic chemicals will become far more dangerous. Fast foods and processed foods are deficient in these vital liver nutrients. Thus although many people are over-eating they are still suffering with malnutrition which exacerbates toxic overload. Dr. Sandra Cabot’s Liver Cleansing Diet reduces the toxic load on the liver and also provides the vital nutrients required by the liver for detoxification.
This is called the conjugation pathway whereby the liver cells add either a glycine or sulphate molecule to a chemical to make it water soluble. It can then be excreted from the body via fluids such as urine or bile. Through conjugation the liver is able to turn drugs (xenobiotics and hormones), neurotransmitters and phenolic compounds into excretable substances. For efficient phase two detoxification the liver requires Vitamin E, carotene, sulphur containing amino acids (taurine, methionine, cysteine), glycine, glutamine, choline and inositol. Cruciferous vegetables (cabbage, cauliflower, broccoli, brussel sprouts) are a good source of natural sulphur compounds for the liver. These things can spike up and support the phase two detoxification system. The liver cleansing diet has been designed to support and enhance the phase one and two liver detoxification systems. If the phase one and two detoxification pathways become overloaded, there will be a build up of toxins in the body. Many of these toxins are fat soluble and incorporate their way into the fatty cell membranes where they may stay for years, if not a lifetime. Some of these toxins, such as pesticides, petrochemicals and aspartame are highly toxic to the nervous system and endocrine glands producing chronic neurological and hormonal dysfunction. They are also carcinogenic and have been implicated in the rising incidence of breast, prostrate and brain cancer. If the filtering and/or detoxification system in the liver are inefficient this will cause harmful substances and micro-organisms to build up in the blood stream. This will increase the workload of the immune system, which may then become overloaded and hyperstimulated. This often is so in symptoms of immune dysfunction such as allergies, inflammatory states, recurrent infections, swollen glands, chronic fatigue or auto-immune disease. These disorders are very common today and usually get treated on a symptomatic basis with drugs. Unfortunately thousands of people visit doctors everyday complaining of these symptoms and rarely does anyone think of the liver. The simplest and most effective way to take the load off the immune system, is to improve liver function. Dr. Sandra Cabot has been able to help many people with chronic immune and liver dysfunction through her LIVER CLEANSING DIET BOOK. In this book she fully explains that you cannot have a healthy immune system if your liver is dysfunctional. This is a revelation for millions of people struggling with poor health. Should the reader be interested, Dr. Cabots book may be ordered by calling 1-888-782-7014.
The Liver Doctor
Calcium-D-glucarate is the calcium salt of D-glucaric acid, a substance produced naturally in small amounts by mammals, including humans. Glucaric acid is also found in many fruits and vegetables with the highest concentrations to be found in oranges, apples, grapefruit, and cruciferous vegetables. (1) Oral supplementation of calcium-D-glucarate has been shown to inhibit beta-glucuronidase, an enzyme produced by colonic microflora and involved in Phase II liver detoxification. Elevated beta-glucuronidase activity is associated wire an increased risk for various cancers, particularly hormone-dependent cancers such as breast, prostate, and colon cancers. (2) Other potential clinical applications of oral calcium-D-glucarate include regulation of estrogen metabolism and as a lipid-lowering agent.
Upon ingestion and exposure to the acidic environment of the stomach, calcium-D-glucarate is metabolized to form D-glucaric acid. D-glucaric acid is further metabolized in the gastrointestinal tract into three compounds existing in equilibrium and comprised of approximately 40-percent D-glucaric acid, 30-percent D-glucaro-1,4-lactone, and 30-percent D-glucaro-6,3-lactone. These compounds are then transported to the blood and various internal organs, and are subsequently excreted in the urine and bile. Although D-glucaro-1,4-lactone seems to be the most pharmacologically active of the three, it is not commercially available. Also, calcium-D-glucarate administration results in longer inhibition of beta-glucuronidase (five hours versus one hour) than does D-glucaro-1,4-lactone, so it is the compound used. (3)
Mechanism of Action
Calcium-D-glucarate’s detoxifying and anticarcinogenic properties are attributed to its ability to increase glucuronidation and excretion of potentially toxic compounds. During Phase II detoxification, chemical carcinogens, steroid hormones, and other lipid-soluble toxins are conjugated with glucuronic acid in the liver (glucuronidation), and excreted through the biliary tract. Beta-glucuronidase is capable of deconjugating these potential toxins, making it possible for them to be reabsorbed rather than excreted. D-glucaro-1,4-lactone is the metabolite that has been shown to inhibit beta-glucuronidase activity, increasing excretion of conjugated xenobiotic compounds and decreasing activity of harmful substances that are most active in their deconjugated state. (4,5) Inhibition of beta-glucuronidase ultimately results in potentially decreasing the risk of carcinogenesis. (6) In addition, by reducing the beta-glucuronidase viability and activity of intestinal bacteria, salts of D-glucaric acid have been shown to enhance enterohepatic circulation and reduce steady state levels of cholesterol synthesis, resulting in decreased serum lipid levels. (7)
Calcium-D-glucarate is not an essential nutrient so, technically, no deficiency state exists. However, since it is only produced in small amounts by humans, it is important that dietary intake be adequate. Diets low in fruits (particularly oranges, apples, and grapefruit) and cruciferous vegetables (broccoli, cabbage, and brussel sprouts) may result in a relative deficiency of calcium-D-glucarate and its metabolites. Research has shown a low level of D-glucaric acid correlates with a higher level of beta-glucuronidase, which in turn is associated with an increased risk for various cancers. (2)
The anticarcinogenic properties of D-glucaric acid and its salts have been studied in various animal tumor models, including colon, (8,9) prostate, (2) lung, (10) liver, (11,12) skin, (13) and breast (14-18) cancer, with the mechanism of action for tumor inhibition being very similar in each. These studies demonstrated decreases in beta-glucuronidase activity, carcinogen levels, and tumorigenesis. The preponderance of research, however, has been conducted on mammary tumors in the rat, the animal model most frequently used for breast cancer research.
A number of studies have shown calcium-D-glucarate alone, and in combination with retinoids, inhibits mammary carcinogenesis in rats by as much as 70 percent. (3) Natural retinoids have been shown to be effective chemopreventive agents at high doses, but unfortunately the cumulative toxic effects of high doses have restricted their prolonged use. Several studies have demonstrated low-dose retinoids in combination with calcium glucarate interact synergistically to inhibit mammary tumor growth in both animal models and human cell lines. (14-18) The mechanisms responsible for the chemopreventive effects of these two agents may be similar. Both retinoids and calcium-D-glucarate inhibit carcinogenesis during the promotion and initiation phases. Calcium-D-glucarate inhibits protein tyrosine kinase-C activity and induces transformation growth factor beta, possibly resulting in an increase in cellular differentiation and slower progression through the cell cycle. (15) Retinoids induce many of these same biochemical effects. (19) Additionally, calcium-D-glucarate enhances glucuronidation and subsequent excretion of carcinogens and other cancer-promoting agents.
Published human studies on calcium-D-glucarate and breast cancer are few but, due to the encouraging results of the animal studies, the National Cancer Institute has initiated a Phase I trial in patients at high risk for breast cancer at Memorial Sloan Kettering Cancer Center. This trial is examining the use of calcium-D-glucarate as an alternative to tamoxifen’s blocking of estrogen receptors. Preliminary results are quite encouraging and due to calcium-D-glucarate’s excellent safety profile, it may be a more effective option than tamoxifen, which has numerous side effects. (3) Other human trials are being conducted at M.D. Anderson Cancer Center in Houston, Texas and AMC Cancer Research Center in Denver, Colorado.
Studies in rats have shown D-glucarate salts to inhibit colon carcinogenesis alone and in combination with 5-fluorouracil (5-FU). In one study, D-glucarate markedly inhibited azoxymethane-induced colon carcinogenesis as evidenced by a 60-percent reduction in both tumor incidence and multiplicity. It was hypothesized that malignant cell proliferation was suppressed by inhibition of beta-glucuronidase. Another possible mechanism may involve alterations in cholesterol synthesis or its conversion to bile acids. (8) The second study demonstrated that salts of D-glucarate, in combination with 5-FU in rat colon tumor explants, resulted in a potentiation of 5-FU’s antitumor activity. D-glucarate alone also showed antitumor activity. (9)
Hepatocarcinogenesis is thought to be preceded by premalignant hepatic foci that are subsequently transformed to malignant cells. Two separate rat studies by a group of researchers at Ohio State University have demonstrated calcium-D-glucarate delays the appearance of altered hepatic foci and significantly inhibits hepatocarcinogenesis, if given during both the initiation and promotion phases. Maximal inhibition was obtained when calcium-D-glucarate was administered by gavage prior to the carcinogenic agent, diethylnitrosamine. (11,12)
A study conducted on mice demonstrated calcium-D-glucarate inhibits benzo[a]pyrene’s ability to bind DNA and induce pulmonary adenomas. (10) Another unpublished phase I clinical trial of 62 patients found D-glucaric acid levels were approximately 29-percent lower in smokers than non-smokers. Regardless of gender, K-ras (an oncogene linked to lung cancer) mutations were found to be present in 38 percent of subjects who smoked, while no K-ras mutations were found in the non-smoking control subjects. It was hypothesized that D-glucaric acid deficiency correlates with K-ras mutations and might be indicative of a higher risk for developing lung cancer. (20)
The efficacy of dietary calcium-D-glucarate as a chemopreventative agent has also been studied in the mouse skin tumorigenesis system. Mice were given 7,12-dimethylbenz[a]anthracene (DMBA) to induce skin tumorigenesis and were fed either a regular chow diet or a chow diet fortified with calcium-D-glucarate. When fed the calcium-D-glucarate chow through both the initiation and promotion phases, papilloma formation was inhibited by over 30 percent. The data indicate that supplementation of calcium-D-glucarate results in a marked alteration in the retention, activity, and metabolism of carcinogenic substances. (13)
Calcium-D-glucarate’s inhibition of beta-glucuronidase activity allows the body to excrete hormones such as estrogen before they can become reabsorbed. Oral administration of large doses of calcium-D-glucarate have been shown to lower serum estrogen levels in rats by 23 percent. (21) Because many breast cancers are estrogen-dependent, calcium-D-glucarate’s ability to affect estrogen and other hormone levels has led to Phase I clinical trials at several major cancer centers in the United States. Results of these studies are pending.
Side effects of currently available hypolipidemic agents present a need for safe and effective lipid-lowering agents. D-glucarates have been shown to significantly reduce total serum cholesterol in rats by as much as 12-15 percent and LDL-cholesterol by 30-35 percent. Preliminary results in humans show D-glucarate reduced total serum cholesterol up to 12 percent, LDL-cholesterol up to 28 percent, and triglycerides up to 43 percent. The lipid-lowering effect of calcium-D-glucarate may be attributed to improved enterohepatic circulation, resulting in increased excretion of bile acids and a reduction in steady state levels of cholesterol biosynthesis. (7)
There are no known drug interactions with calcium-D-glucarate, but many drugs and hormones are metabolized in the liver via glucuronidation. Therefore, taking calcium-D-glucarate may increase elimination of these substances, possibly reducing their effectiveness.
Side Effects and Toxicity
No adverse effects have been observed after prolonged feeding to rats or mice at concentrations of 70, 140, or even 350 mmol/kg. (6) Preliminary results of clinical trials in humans have shown calcium-D-glucarate is without adverse effects.
The recommended oral dosage of calcium-D-glucarate is generally in the range of 1500-3000 mg daily. Until human trials have been completed the optimal dosage remains elusive.
(1.) Dwivedi C, Heck WJ, Downie AA, et al. Effect of calcium glucarate on beta-glucuronidase activity and glucarate content of certain vegetables and fruits. Biochem Med Metab Biol 1990;43:83-92.
(2.) Walaszek Z, Szemraj J, Narog M, et al. Metabolism, uptake, and excretion of a D-glucaric acid salt and its potential use in cancer prevention. Cancer Detect Prev 1997;21:178-190.
(3.) Heerdt, AS, Young CW, Borgen PI. Calcium glucarate as a chemopreventive agent in breast cancer, Isr J Med Sci 1995;31:101-105.
(4.) Horton D, Walaszek Z. Conformations of the D-glucarolactones and D-glucaric acid in solution. Carbohydr Res 1982;105:95-109.
(5.) Walaszek Z, Hanausek-Walaszek M. D-glucaro-1,4-lactone: its excretion in the bile and urine and effect on biliary excretion of beta-glucuronidase after oral administration in rats. Hepatology 1988;9:552-556.
(6.) Selkirk JK, Cohen GM, MacLeod MC. Glucuronic acid conjugation in the metabolism of chemical carcinogens by rodent cells. Arch Toxicol 1980;139:S171-S178.
(7.) Walaszek Z, Hanausek-Walaszek M, Adams AK, Sherman U. Cholesterol lowering effects of dietary D-glucarate. FASEB 1991;5:A930.
(8.) Yoshimi N, Walaszek Z, Moil H, et al. Inhibition of azoxymethane-induced rat colon carcinogenesis by potassium hydrogen D-glucarate. Int J Oncol 2000;16:43-48.
(9.) Schmittgen TD, Koolemans-Beynen A, Webb TE, et al. Effects of 5-fluorouracil, leucovorin, and glucarate in rat colon-tumor explants. Cancer Chemother Pharmacol 1992;30:25-30.
(10.) Walaszek Z, Hanausek-Walaszek M, Webb TE. Dietary glucarate-mediated reduction of sensitivity of murine strains to chemical carcinogenesis. Cancer Lett 1986;33:25-32.
(11.) Oredipe OA, Barth RF, Hanausek-Walaszek M, et al. Effects of an inhibitor of beta-glucuronidase on hepatocarcinogenesis. Proc Am Assoc Cancer Res 1987;28:156.
(12.) Oredipe OA, Barth RF, Hanausek-Walaszek M, et al Effects of calcium glucarate on the promotion of diethylnitrosamine-initiated altered hepatic loci in rats. Cancer Lett 1987;38:95-99.
(13.) Dwivedi C, Downie AA, Webb TE. Modulation of chemically initiated and promoted skin tumorigenesis in CD-1 mice by dietary glucarate. J Environ Path Toxicol Oncol 1989;9:253-259.
(14.) Abou-Issa H, Koolemans-Beynen A, Meredith TA, Webb TE. Antitumour synergism between non-toxic dietary combinations of isotretinoin and glucarate. Eur J Cancer 1992;28:784-788.
(15.) Webb TE, Abou-Issa H, Stromberg PC, et al. Mechanism of growth inhibition of mammary carcinomas by glucarate and the glucarate:retinoid combination. Anticancer Res 1993; 13:2095-2100.
(16.) Bhatnagar R, Abou-Issa H, Curley RW, et al. Growth suppression of human breast carcinoma cells in culture by N-(4-hydroxyphenyl) retinamide and its glucuronide and through synergism with glucarate. Biochem Pharmacol 1991 ;41:1471-1477.
(17.) Curley RW, Humpries KA, Koolemans -Beynan A, et al. Activity of d-glucarate analogues: synergistic antiproliferative effect in cultured human mammary tumor cells appear to specifically require the d-glucarate structure. Life Sci 1994;54:1299-1303.
(18.) Abou-Issa H, Moeschberger M, Masry EI, et al. Relative efficacy of glucarate on the initiation and promotion phases of rat mammary carcinogenesis. Cancer Res 1995;15:805-810.
(19.) DeLuca LM. Retinoids and their receptors in differentiation, embryogenesis and neoplasia. FASEB J 1991;5:2924-2933.
(20.) Walaszek Z, Raich PC, Hanausek M, et al. Role of D-glucaric acid in lung cancer prevention. Unpublished research. AMC Cancer Research Center, Denver, CO.
(21.) Walaszek Z, Hanausek-Walaszek M, Minto JP, Webb TE. Dietary glucarate as anti-promoter of 7,12-dimethylbenz[a]anthracene-induced mammary tumorigenesis. Carcinogenesis 1986;7:1463-1466.
COPYRIGHT 2002 Thorne Research Inc.
Merck admits injecting cancer viruses (SV40 and others) in millions
Folks, you had better sit down, take a very deep breath. Merck drug company vaccines admits injecting cancer viruses into their vaccines and we have the proof on video for you to watch.
This censored interview conducted by medical historian Edward Shorter for WGBH public television (Boston) and Blackwell Science was cut from The Health Century due to its liability–the admission that Merck drug company vaccines have traditionally been injecting cancer viruses (SV40 and others) in people worldwide.
This segment of In Lies We Trust: The CIA, Hollywood & Terrorism, produced and freely contributed by consumer protector and public health expert, Dr. Leonard Horowitz, features the world’s leading vaccine expert, Dr. Maurice Hilleman, who explains why Merck’s vaccines have spread AIDS, leukemia, and other horrific plagues worldwide.
Dr. Hilleman, who developed the Mumps, Rubella and Measles vaccines, said: “Vaccines are the bargain basement technology of the 20th century.”
In the taped interview (with about 6 Merck executives in the room, their nervous laughter audible in the tape) Dr. Hilleman explains how in his search for uninfected monkeys, Merck imported green monkeys from Africa. Those monkeys, it turned out, were carrying the AIDS virus: “I didn’t know we were importing AIDS.”
Dr. Hilleman also acknowledged that he discovered that the Sabine polio vaccine (manufactured by Merck) was infected with the SV-40 cancer virus. In the process of developing vaccines Merck scientists are shown to blithely disregarded public safety as they conducted massive tests exposing millions of unsuspecting people to wild viruses. Dr. Hilleman acknowledged that the cancer infected polio vaccine had been tested in massive field trials in Russia, then in the U.S.
The issues raised in this candid interview raise serious doubts about the propaganda the public has been fed about the safety of vaccines. Vaccines that have been promoted as “safe and effective” miraculous cures have been infecting (possibly) millions of people with cancer, leukemia, and AIDS.
The interview was conducted by Dr. Edward Shorter, Professor of the History of Medicine and Professor of Psychiatry, University of Toronto. I checked the authenticity of the tape with Dr. Shorter who informed me that he did it when preparing a PBS series called “The Health Century.” Doubleday published a companion volume of the same title in 1987.
Dr. Shorter deposited the entire tape of the interview, including portions omitted from the book, along with other interviews in the National Library of Medicine.
The uncovered facts should prompt a re-examination of the advisability of US mandatory vaccine policies–
The person who posted this censored portion of the interview on Youtube is Dr. Leonard Horowitz, a controversial and prolific healthcare expert with multiple academic degrees–including 3 doctorates.
In his forthcoming documentary film, “In Lies We Trust: The CIA, Hollywood & Bioterrorism,” Dr. Horowitz examines official directives for national preparedness against outbreaks, nuclear explosions, and other disasters. A critical examination of what officials are saying and not telling that impacts the future of public health and urgent life-saving decisions every American is currently being encouraged to make.
In short you have been deliberately poisoned.
Others see a link between vaccinations and satanic rituals or witchcraft, where animals are sacrificed and their organs brewed in a hellish concoction of horrid substances: voodoo medicine by 21st century mad scientists. Sadly, our children are their unwilling subjects as society is slowly devoured by their insatiable appetite for human experimentation.
Please forward this clip (link) to everyone you know who thinks vaccines are “safe and effective.”