Guest guest Posted August 15, 1999 Report Share Posted August 15, 1999 > August 12th, 1999 > > Congressman Dan Burton > Chairman > Government Reform Committee > US House of Representatives > 2157 Rayburn House Office Building > Washington, DC 20515 > > Dear Congressman Burton, > > This letter is in support of your Government Reform Committee on Vaccines; > Finding the Balance Between Public Safety and Personal Choice. After > speaking with your staff member, Mrs. Beth Clay, I had to forward you the > appalling story regarding the death of our son, . I have also > included some of the facts that my husband and I have uncovered since our > son's death that link vaccination with brain cancer. > > On August 10th, 1998 our only child, , was diagnosed with the most > common pediatric brain cancer, medulloblastoma. He was two years old. Our > lives were shattered. The next six months became a race against time to try > to understand the disease, find the appropriate treatment, and save . > > After two brain operations recovered quickly. We wanted to give our > son the most effective cancer therapy possible. After weeks of research, > many conversations with parents who had children with brain cancer, and > conversations with doctors from all over the world, we selected the Burzynski > Clinic in Houston, Texas. We arrived there and incredibly we were turned > away. Dr. Burzynski said he was not allowed to accept . I'll never > forget it. We sat in an examining room. was smiling at the doctor. > > " Why can't you take ? " I asked Burzynski. > > " The FDA dictates who I can and can't accept, " Burzynski said. > > Burzynski explained to us that the FDA would only allow him to accept > children who had suffered through chemotherapy and/or radiation and still had > " measurable tumor " left in their brains. hadn't had either of > these " world class treatments " but already endured two brain operations (16 > hours of surgery in total) and was tumor free for the moment. He had paid a > dear price to be tumor free. His optic nerves had been injured so that his > big brown eyes were stuck pointing in opposite directions, he lost the > ability to cry and laugh and he temporarily lost the ability to walk. > > " Please accept my son. He's only two years old. His whole life is in front > of him. I know your treatment works. I've spoken to several parents whose > children are here. They had malignant brain tumors like but now > they're alive and well. You have to treat my son, " I begged. > > Dr. Burzynski said simply, " I am sorry but I can't. " Burzynski was saddened but he > was powerless. The FDA had made him turn away many children just like . > Chemotherapy was started soon after and died in my arms three months later. > > Because of the FDA, Dr. Burzynski has to turn away over 90% of the cancer > victims who come to him, many of them children. Burzynski's cancer therapy > is non-poisonous to the body and light years ahead of the crude poisonous > treatments - chemotherapy or radiation - offered by conventional medicine. > If Burzynski could accept and other children like him his cure rate > would increase. It's a clever ploy on the part of the FDA to only allow Dr. > Burzynski to accept children who have already had chemotherapy and/or > radiation and whose cancer has returned. Then nothing can save those > children. When 's cancer returned while he was on chemotherapy, he > died within two weeks. > > Who is the FDA really protecting? Why would the FDA not want Dr. Burzynski > to have a high cure rate? Dr. Burzynski's therapy is a better product - it > is not toxic to the body and it is much more effective against cancer. But > every year, chemotherapy and radiation gross tens of billions of dollars for > the drug companies and the medical establishment. If Dr. Burzynski's > treatment was allowed to be accessible, imagine the market share it would > take from chemo and radiation. Imagine the money it would cost the drug > companies and the cancer doctors. It could literally cost them billions. > > Lederle, the same company that produces vaccinations, manufacturers the > chemotherapy that killed ! was originally diagnosed with > medulloblastoma. The cancer that took his life was called leptomeningeal > sarcoma. How did one cancer turn into another? By the carcinogenic (by > definition the " DNA changing " ) effects of chemotherapy. In fact, nearly all > chemotherapy drugs are listed as " Class I - Known Human Carcinogens " with the > FDA. Yet every day hundreds of children are injected with these deadly > chemicals. > > 's immune system was completely destroyed by the chemo and he had no > strength to fight the new cancer. > > Whether we are talking about childhood vaccinations, therapy for cancer, > treatments for cardiovascular diseases or any of the other big money makers, > the interests, motives and actions of the federal government are completely > inseparable with the motives and goals of the drug producers and the AMA > leadership. After all, we are talking about the exact same people. The same > doctors who work for the major drug companies and own stock in those > corporations take a rotation through the FDA. They will work at this > governmental " regulatory " body for a few years, make decisions that protect > their investments and careers, and then return to the drug companies for > reportedly bigger salaries and stock options. Over the last twenty years, > the most powerful people at the FDA have been employees, grant recipients, > board members or research " affiliates " of the major pharmaceutical > corporations. > > WHY DID ALEXANDER GET CANCER? > THE VACCINE-RELATED SYMPTOMS > Why did our strong two-year-old boy have a brain tumor? There is no cancer > on either side of our families going back three generations. Both of our > paternal grandmothers lived to almost 90! Two of 's > great-grandparents are still alive today. > > My husband and I started to review everything we knew about 's > health. never had been a good sleeper. At four months old, when > most babies start to sleep through the night, actually got worse. > He used to wake us up at least four times a night and yell. We also recalled > an evening when was about seven months old. It was a couple of > weeks after he had received his latest round of vaccinations shots. He > started crying very loud and long and he suddenly had convulsions that lasted > about five minutes. I held him in my arms. He calmed down but it had made > him very tired. The next day I called his pediatrician. I was told that > little children sometimes get excited and can have spasms. It was nothing I > should worry about. A couple months later, would have another > episode of " spasms. " > > After the age of one, began to have eczema outbreaks that would > cover the back of his legs. I went to the pediatrician. He said that lots > of little children have food allergies and he gave me cortisone cream. The > cream didn't help very much. I used vitamin E and almond oil, which seemed > to help a little. > > But why would get cancer? He always had been a good eater. He was > very strong and tall for his age- in the top 95 percentile in weight and > height compared to other children. We didn't live near a nuclear plant, I > didn't work near pesticides. My husband worked in an office. Since 1992, we > had lived in Marina del Rey, a suburb by the beach in Los Angeles. Of > course, Los Angeles is not known for its fresh air, but none of his little > friends had cancer. > > We started to do research on medulloblastoma - the brain tumor that > was originally diagnosed with. The tumor had been identified in the 1920's > by two of the first neurosurgeons, Drs. Percival and Harvey Cushing. > They removed medulloblastomas and other brain tumors at the Surgical Clinic > of the Bent Brigham Hospital in Boston. We read their articles and > books and studied their graphs on the survival rates of children with > medulloblastoma. We learned that after " 100% " of the tumor had been > surgically removed it would grow back within six to twelve months (assuming > no additional therapy was attempted). This suggested to us that the original > tumor took approximately that same amount of time to grow. > > had been very irritable and threw up a lot in November 1997. The > pediatrician told me it was a viral infection, a stomach flu. > often had ear infections around this time. Then in March 1998, > threw up again and told me he had pain in his tummy. I thought he had > swallowed a button or little toy. That night, the pediatrician on call told > us to go to the emergency room. There, threw up more. The ER > doctor told us that had a viral infection. The next day, his > pediatrician told me the same thing. This was five months before he would > be diagnosed with a three-inch malignant tumor growing in his brain. > > We now understand that sometime between November 1997 and March 1998 the > tumor began to grow. What had happened to at or before that time which > > could have led to cancer? I opened 's " medical file " and suddenly saw all > > the vaccines he received within weeks or months of these symptoms. My husband > and I focused on the DPT, the IPV and OPV and Hepatitis B vaccine. What were > these vaccines all about? What was in them? And more importantly what were > the side effects on an infant's brain? > > THE VACCINE CANCER CONNECTION > After extensively researching the medical literature, we have identified six > ways that vaccination may cause cancer, either directly or indirectly. After > reading this you may wonder why aren't these subjects being actively pursued? > Childhood cancer is on the rise, why aren't the " authorities " conducting > objective research to determine the risks? The answer is simple - money. > Nearly all the medical research in this country is funded by drug companies > or the U.S. government (viz. taxpayer's money). Both parties have an > inherent interest in, at a minimum, maintaining the status quo. What would > motivate a drug company to pay for a study that demonstrates that their > products cause cancer? Do they want to commit fiscal suicide? Why would the > federal government pay for research that presents the dangers of a program > that they have ostensibly mandated? > > ORTHODOX MEDICINE HAS NO IDEA IF VACCINES ARE CARCINOGENIC > We will begin with a very basic question - are vaccines carcinogenic? And > the answer is that nobody knows because no studies have ever been done. The > inserts that the vaccine manufacturers must place with each and every vial of > vaccine state this fact. Here's a summary of what the vaccine manufacturers > publish about their products for the eyes of physicians. This information is > taken directly from their inserts as it is published in the Physicians' Desk > Reference (PDR, 51st edition, Medical Economics Co. Inc., 1997). The last > column is of most interest. > > VACCINE - MANUFACTURER - BRAND NAME - AGES - STUDIES ON CARCINOGENIC > POTENTIAL ACCORDING TO MANUFACTURER > Chickenpox (Varicella) Merck Varivax 12 months and older No > studies conducted > > DTP Lederle Tetramune 2 months to 5 years " Tetramune has > not been evaluated for its carcinogenic or mutagenic potential. " > > DTP Lederle Tri-Immunol 2 months to 7 years No studies > conducted > > DTP Connaught (subsidiary of Pasteur Merieux) Tripedia 15 months to 7 > years " Tripedia has not been evaluated for its carcinogenic or mutagenic > potential. " > > DTP Lederle Acel-Immune 17 months to 7 years " Acel-Immune has not been > evaluated for its carcinogenic or mutagenic potential " > > DTP(whole cell pertussis) Kline Beecham 6 weeks to 7 years " Animal > and human studies concerning possible carcinogenic or teratogenic effects > have not been done. " > > Hepatitis A Kline Beecham > (subsidiary of Pasteur Merieux) Havrix Over two years old " Havrix has not > been evaluated for its carcinogenic or mutagenic potential. " > > Hepatitis B Merck Recombivax " infants " No studies > conducted > > Influenzae type b Haemophilus b conjugate with diphtheria protein Lederle > HibTITER 2-71 months " HibTITER has not been evaluated for its carcinogenic > or mutagenic potential. " > > Influenzae type b Haemphilus b conjugate with tetatus toxoid conjugate > Connaught (subsidiary of Pasteur Merieux)ActHIB 2 months to 5 years > No studies conducted > > Japanese encephalitis virus Connaught (subsidiary of Pasteur Merieux) > JE-VAX One year and older " No studies have been performed to evaluate > carcinogenicity or mutagenic potential. " > > Measles live Merck Attenuvax 15 months and older No studies > conducted > > Measles, Mumps, Rubella live Merck M-M-R 15 months and older No > studies conducted > > Measles, Rubella (live) Merck M-R-Vax 15 months and older No studies > conducted > > Mumps (live) Merck Mumpsvax 12 months and older No studies > conducted > > Polio (live) Lederle Orimune 6 weeks to 18 years No studies conducted > > Poliovirus (inactivated) Connaught (subsidiary of Pasteur Merieux) IPOL > " infants, children and adolescents " " Studies in animals to evaluate > carcinogenic potential have not been conducted. " > > Rubella and mumps (live) Merck Biavax II 12 months and older No > studies conducted > > Rubella (live) Merck Meruvax 12 months to puberty No studies conducted > > None of the vaccines injected into children have ever been tested for their > carcinogenic (cancer causing), mutagenic (mutation causing), or teratogenic > (developmental malformation causing) potential. Not a single one. Can these > chemicals that are injected into healthy children cause cancer? The people > manufacturing the vaccines (the drug companies) and the bureaucrats mandating > the drugs can't say because no studies have ever been conducted. > > In summary, federal and state governments are mandating that infants and > children swallow and be injected with substances that have never been tested > for their ability to cause cancer, mutations or developmental malformations. > In the meantime, the drug companies are grossing billions of dollars on sales > of these potentially carcinogenic products. > > HOW VACCINATION CAN CAUSE OR CONTRIBUTE TO CANCER > > VACCINES CONTAIN KNOWN CARCINOGENS > > If you call the American Association of Pediatrics and ask them what is the > safe dosage of mercury derivatives, aluminum and formaldehyde to be injected > into an infant, they may suspect child abuse. After they have calmed down, > they will explain that there is no safe dosage because these are all > potentially carcinogenic substances. But mercury derivatives, aluminum and > formaldehyde are ingredients in most vaccines. How is it possible that > they're safe? The answers depends on who is injecting them. If you or I > inject our child with mercury or formaldehyde we are going to jail. But if a > drug company and a doctor inject the same chemicals then they are perfectly > safe. > > VIRUSES CAN BE CARCINOGENIC > Vaccines are comprised of viruses and viruses can be carcinogenic. According > to mainstream science a number of viruses with oncogenic (cancer causing) > properties have been identified over the last twenty years. The information > below comes from the chapter entitled " Etiology of Cancer: Viruses " from the > 5th edition of the book - Cancer: Principles & Practice of Oncology. (One of > the book's editors is Dr. De Vita, Jr., former director of the > National Cancer Institute.) This chapter lists various viruses and the > cancers associated with them: > > Virus And the Human Cancer associated with them: > Hepatitis B Hepatocellular carcinoma > Hepatitis C Hepatocellular carcinoma > Epstein-Barr Burkitt's lymphoma > Epstein-Barr Hodgkins disease > Epstein-Barr Immunoblastic lymphoma > HPV-16, HPV-18, 33, 39 Anogenital cancers and some upper airway cancers > HPV-5, HPV-8, HPV-17 Skin cancer > BK, JC Brain tumors (possible), Mesotheliomas (possible) > HTLV-I, Adult T-cell leukemia/lymphoma > HTLV-II Hairy cell leukemia > > Murnane Poeschla E, Wong-Staal F. Etiology of Cancer: Viruses, p.169, Cancer: > Principles & Practice of Oncology; Fifth Edition, edited by V. T. DeVita Jr., > S. Hellman, S. A. Rosenberg. Lippincott-Raven Publishers, Philadelphia, 1997. > > The association between some viruses and some cancers is a well-accepted > medical fact. Are there other viruses that may cause or lead to other > cancers? Of course. There are literally tens of thousands of viruses, but > only a small percentage has been tested for their ability to cause cancer. > In fact, some viruses use a " team approach. " One virus by itself may be > relatively benign but when it is combined with other viruses it " helps " the > first one cause cancer. These viruses are literally called " helper viruses. " > How many various combinations of different viruses can lead to cancer, no > one knows. But when you consider that: > > Ø Children are injected with bacteria (that contain viruses) > Ø Children are injected with viruses themselves as per the vaccine > Ø The bacteria and virus vaccines are grown on animal tissue (i.e. monkeys, > eggs, etc.) that also contain their own population of viruses > > There is no way of knowing what viral combinations have formed and what is in > the final " soup " that will be injected into a healthy infant. The toxicity > test that vaccine manufacturers use is as crude as can be imagined. They > inject mice with the vaccines and if a given percentage still eat and put on > weight than the vaccine is pronounced safe for children. Unbelievable! > > VACCINES, BRAIN INJURY AND BRAIN CANCER > Oncologists and neurosurgeons at Children's Hospital Los Angeles, St. Jude > Children's Research Hospital and UCLA Medical Center told us that pediatric > brain cancer is on the rise? Why? Why are more and more children getting > cancer in their brains? Could it be due to the various types of brain > injuries caused by vaccines? > > The fact that vaccines can cause temporary or permanent brain damage is an > established fact. Even the manufacturers admit it. For example, the > manufacturer of one of the DTP vaccines (Lederle), warns pediatricians on > their insert that their vaccine can cause " neurological complications such as > convulsions, encephalopathy, and various mono and polyneuropathies including > Guillian-Barre Syndrome.Permanent neurological disability and death have been > reported. " > > - Physicians' Desk Reference, 51st edition, Medical Economics Co. Inc., 1997 > > There is an abundance of medical literature going back one hundred years that > suggests a connection between cancer and chronic injury caused by viruses or > bacteria. It appears that cancers have a tendency to form in organs that are > injured or irritated by viral or bacterial infections. For example, it is > well known that people who have various forms of hepatitis (viruses that > infect the liver) are at a much higher risk for liver cancer. This fact was > presented in a recent article published in the European Journal of Cancer > Prevention. The authors wrote, " Chronic disease conditions.are well > established as risk factors for cancer development. These may be due to > viruses (for example, in the case of hepatitis and liver cancer), bacterial > infections, parasite infestation or physical trauma. " > > - , MA, Tsuda H, Chronically elevated proliferation as a risk factor for > neoplasia. European Journal of cancer Prevention 1988 October; 7(5): 353-385. > > The same line of reasoning suggests that a viral infection of the brain > (which vaccines are known to cause) can lead to cancer of the brain. It's a > rational conclusion and a reasonable question to ask, but no one from the > drug companies or the federal government is asking it. > > SIMIAN VIRUS 40 > In the 1950's and 1960's the polio vaccine injected into millions of children > contained an unexpected guest - another virus that was growing on the same > monkey kidney cells in which the vaccine was being grown. This virus was > named Simian Virus 40 (SV40) because it was the 40th simian or monkey virus > found. Unfortunately, this virus was also found to cause cancer. The > vaccine manufacturers changed their monkeys (African green monkeys) but this > wasn't enough. Today SV40 is found in many human cancers including many > pediatric brain cancers. Coincidence? I don't think so. It turns out that > SV40 can be passed horizontally (i.e. between father and mother) and > vertically (i.e. between mother and child). In fact, SV40 is often > associated with medulloblastoma, the most prevalent pediatric brain tumor. > When scientists injected young hamsters with Simian Virus 40 over 80% > developed brain cancers - all of which were medulloblastomas. Here are a few > of the studies that have looked at SV40 and human cancers: > > Ø In 1979, Drs. Jaqueline Farwell, Dohrmann, Lorraine Marrett and J. > Wister Meigs wrote a paper entitled: Effect of SV40 Virus-Contaminated Polio > Vaccine on the Incidence and Type of CNS Neoplasms in Children: A > Population-Based Study, in which they found a substantial increase in > childhood brain tumors, especially medulloblastoma, when the mothers had been > inoculated with vaccines containing SV40. They wrote: > > " In the late 1950's and early 1960's, an increase occurred in the number of > central nervous system tumors diagnosed in children as recorded in the > Connecticut Tumor Registry. From 1955 to 1961, polio vaccine was used in > Connecticut, which subsequently was found to contain the virus SV40. In > animal models SV40 has produced central nervous system tumors. particularly > striking rises in gliomas (astrocytoma, spongiblastoma, and glioblastoma > multiforme) and medulloblastomas were noted in children born during > 1956-1962.Among medulloblastoma patients, 10 of 15 were exposed to SV40. > This rate of exposure is high and significantly greater than among controls > (children without brain tumors).SV40 may selectively induce malignant > tumors.In summary we demonstrate a strong association between exposure to > SV40 and the development of medulloblastoma.(and) the occurrence of gliomas. " > > Ø In 1987, Drs. Roush, Theodore Holford, Schymura and Colin > White of the Yale University School of Medicine published a book on cancer > risks. In it they wrote: > > " Infectious agents have been strongly associated with childhood brain tumors. > An excess of central nervous system malignancies occurred in a cohort (a > group) of offspring (children) whose mothers were inadvertently exposed to > polio vaccine contaminated by Simian Virus 40 (SV40). Medulloblastomas bore > the strongest relationship to the contaminated vaccine. " > > - Roush G, Holford TR, Schymura MJ, White C, Cancer Risk and Incidence > Trends: The Connecticut Perspective, Brain, Cerebral Meninges, and Cranial > Nerves, Ages 0-19, Department of Epidemiology and Public Health Yale > University School of Medicine; The Hemisphere Publishing Company, 1987. > > Ø In this 1995 study published in the Journal of the National Cancer > Institute, SV40 was again found in various human brain tumors but not in any > healthy brain tissue. The researchers wrote: > > " .we found SV40 DNA sequences in five of six choroid plexus papillomas, eight > of eleven ependymomas, three of seven astrocytomas.None of the 13 normal > brain tissues were positive for SV40 DNA. " > > - i F, et. al., Human Brain Tumors and Simian Virus 40, Journal of the > National Cancer Institute, September 6, Volume 87, 1995 > > Ø In 1997, when researchers looked for SV40 in other human cancers such as > mesotheliomas (a kind of lung cancer), and osteosarcomas (a kind of bone > cancer that kills children and adults), they found them. The doctors wrote: > > " We decided to test human mesotheliomas and osteosarcomas for SV40 based > on.the enormous increase in the incidence of mesotheliomas in the second half > of this century which coincided with the inadvertent inoculation of millions > of people with SV40 contaminated polio vaccines. SV40 or closely related DNA > sequences are present in specific types of human tumors. " > > - Rozzo P, et. al, Evidence for and implications of SV40-like sequences in > human mesotheliomas and osteosarcomas; Conference: SV40 a Possible Human > Polyomavirus National Institute of Health January 27 and 28, 1997 > > Ø This paper, like the previous one, was presented at an SV40 seminar at the > National Institute of Health in 1997. In it the authors state that SV40 is > found in most brain cancers and that it can spread from one generation to the > next. They also mention that more people who are vaccinated have brain > tumors versus those who have not been vaccinated. They wrote: > > " SV40 amplification products were detected at high prevalence in primary > human brain tumors: 83% of choroid plexus papillomas, 75% ependymomas, 47% > astrocytomas, and 37% glioblastomas.35% osteosarcomas, and Ewing's > tumors.These results indicate that SV40 is associated with human brain and > bone neoplasms (cancers).SV40 infection (may be spread) by blood transfusion > and sexual transmission in the human population. > > " .a viral co-factor should be taken into consideration as a possible cause > of. human brain and bone tumors.a higher incidence of brain neoplasms (brain > cancers) was noted in cohorts (groups) of vaccinated persons. In this as > well as in other studies, a high prevalence of SV40 was detected in brain and > bone tumors that affect early childhood. " > > - i F, et. al, Simian Virus footprints in normal human tissues, brain > and bone tumors of different histotypes; Conference: SV40 a Possible Human > Polyomavirus - National Institute of Health January 27 and 28, 1997 > > Ø And in this most recent study published in January of this year, > researchers found SV40 in all the brain tumors they examined. They wrote: > > " We found SV40.sequences in all brain tumor types investigated. High > frequencies were found in low-grade astrocytomas, anaplastic astrocytomas and > secondary glioblastomas (59%).Presence of viral DNA was also found in > pediatric brain tumors. " > > - Huang H, et al, Identification in human brain tumors of DNA sequences > specific for SV40 large T antigen, Brain Pathology, January 9, 1999 > > So here's the obvious question - Is the SV40 from the 1950's and 1960's back > to haunt us? Are parents passing cancer on to their children? > > (Continued on Part II) Quote Link to comment Share on other sites More sharing options...
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