Guest guest Posted July 27, 2000 Report Share Posted July 27, 2000 At 09:03 AM 07/27/2000 -0400, you wrote: > > >I was also send this phrase. Does it hold any merit. It is the only thing >my friend will vaccinate for: and its the WORST one! > >Hepatitis B (the >only one with an approved vaccination so far) is an untreatable viral liver >disease. There are simply no medicines with which to treat it. > >Diane http://www.909shot.com/newsletterexcerpts.htm Excerpts from " Hepatitis B Vaccine - The Untold Story " THE VACCINE REACTION " When it happens to you or your child, the risks are 100% " Published by the National Vaccine Information Center Barbara Loe Fisher, Editor Excerpts from " HEPATITIS B VACCINE: THE UNTOLD STORY " Hepatitis B Not Highly Contagious - Unlike other infectious diseases for which vaccines have been developed and mandated in the U.S., hepatitis B is not common in childhood and is not highly contagious. Hepatitis B is primarily an adult disease transmitted through infected body fluids, most frequently infected blood, and is prevalent in high risk populations such as needle using drug addicts; sexually promiscuous heterosexual and homosexual adults; residents and staff of custodial institutions such as prisons; health care workers exposed to blood; persons who require repeated blood transfusions and babies born to infected mothers. According to CDC Prevention Guidelines: A Guide to Action (1997), a book written by federal public health officials at the U.S. government Centers for Disease Control (CDC), " the sources of [hepatitis B] infection for most cases include intravenous drug use (28%), heterosexual contact with infected persons or multiple partners (22%) and homosexual activity (9%). " According to on's Principles of Internal Medicine (1994), mother to child transmission of hepatitis B " is uncommon in North America and western Europe. " Although CDC officials have made statements that hepatitis B is easy to catch through sharing toothbrushes or razors, Mast, M.D., Chief of the Surveillance Section, Hepatitis Branch of the CDC, stated in a 1997 public hearing that: " although [the hepatitis B virus] is present in moderate concentrations in saliva, it's not transmitted commonly by casual contact. " Hepatitis B Not A Killer Disease For Most - Symptoms of hepatitis B disease include nausea, vomiting, fatigue, low grade fever, pain and swelling in joints, headache and cough that may occur one to two weeks before the onset of jaundice (yellowing of the skin) and enlargement and tenderness of the liver, which can last for three to four weeks. Fatigue can last up to a year. According to on's, in cases of acute hepatitis B " most patients do not require hospital care " and " 95 percent of patients have a favorable course and recover completely " with the case-fatality ratio being " very low (approximately 0.1 percent). " Those who recover completely from hepatitis B infection acquire life-long immunity. Of those who do not recover completely, fewer than 5 percent become chronic carriers of the virus with just one quarter of these in danger of developing life threatening liver disease later in life, according to Robbins Pathologic Basis of Disease (1994), a medical college textbook. The Guide to Clinical Preventive Services (1996), written under the supervision of the U.S. Department of Health and Human Services (DHHS), states that the risk of developing a chronic hepatitis B infection is higher in infected infants than in infected older children and adults: " Infections during infancy, while estimated to represent only 1-3% of cases, account for 20-30% of chronic infections. " Because infants born to infected mothers are at highest risk for developing chronic hepatitis B infections, routine screening of pregnant women for hepatitis B infection is one of the most important public health measures that can be taken to prevent chronic hepatitis B carriers. The Merck Manual (1992), a major medical reference used by physicians, notes that " postexposure vaccination is recommended for newborn infants of hepatitis B positive mothers. " Hepatitis B Low In U.S. - The U.S. and western Europe have always had among the lowest rates of hepatitis B disease in the world (0.1% to 0.5% of the general population) compared to countries in the Far East and Africa, where the disease affects 5-20% or more of the population. According to Guide to Clinical Preventive Services, in the U.S. " the greatest reported incidence [of hepatitis B] occurs in adults aged 20-39 " and " the number of cases peaked in 1985 and has shown a continuous gradual decline since that time. " Even though hepatitis B disease is uncommon in the general population in the U.S., it continues to be high among those engaged in high-risk behaviors, especially IV drug use. Guide to Clinical Preventive Services states that " In recent years, a growing number of injection drug users have become infected; currently, between 60% and 80% of persons who use illicit drugs parenterally (through the skin such as with a needle stick) have serologic evidence of [hepatitis B] infection. " In 1991, there were 18,003 cases of hepatitis B reported in the U.S. out of a total U.S. population of 248 million. According to the October 31, 1997 Morbidity and Mortality Weekly Report published by the CDC, in 1996 there were 10,637 cases of hepatitis B reported in the U.S. with 279 cases reported in children under the age of 14 and the CDC stated that " Hepatitis B continues to decline in most states, primarily because of a decrease in the number of cases among injecting drug users and, to a lesser extent, among both homosexuals and heterosexuals of both sexes. " CDC Recommends All Infants Get Hep B Vaccine - Even though hepatitis B is an adult disease, is not highly contagious, is not deadly for most who contract it, and is not in epidemic form in the U.S. (except among high risk groups such as IV drug addicts), in 1991 the Advisory Committee on Immunization Practices (ACIP) of the Centers for Disease Control (CDC) recommended that all infants be injected with the first dose of hepatitis B vaccine at birth before being discharged from the hospital newborn nursery. A similar recommendation was also made by the Committee on Infectious Diseases of the American Academy of Pediatrics (AAP). This, despite the fact almost nothing is known about the health and integrity of an individual baby's immune and neurological systems at birth. In 1991, media reports generated by the CDC used hepatitis B disease statistics that were not anchored in documented fact but are still used today to promote mass hepatitis B vaccination. Most of the inflated disease statistics originate with statements generated by the Centers for Disease Control. In the 1991 ACIP Recommendations calling for mass vaccination with hepatitis B vaccine published in the Morbidity and Mortality Weekly Report, the CDC states that there are an " estimated 1 million-1.25 million persons with chronic hepatitis B infection in the United States " and that " each year approximately 4,000-5,000 of these persons die from chronic liver disease " and that " an estimated 200,000-300,000 new [hepatitis B] infections occurred annually during the period 1980-1991. " The CDC gives no scientific reference for this data other than the CDC. Just one year before the government's call for mass vaccination, hepatitis B vaccine maker Kline Beecham in their 1990 hepatitis B vaccine product insert stated, " The CDC estimates that there are approximately 0.5 to 1.0 million chronic carriers of hepatitis B virus in the U.S. and that this pool of carriers grows by 2% to 3% (12,000 to 20,000 individuals) annually. " Hep B Vaccine Licensed By FDA Without Adequate Proof of Long Term Safety - In 1986, the FDA gave Merck & Co. a license to market the first recombinant DNA hepatitis B vaccine, which replaced the old hepatitis B vaccines made from blood taken from human chronic hepatitis B virus carriers. In awarding Merck & Co. and, later, Kline Beecham Pharmaceuticals, licenses to market their genetically engineered hepatitis B vaccines in the U.S., the FDA allowed both drug companies to use " safety " studies which only included a few thousand children monitored for only four or five days after vaccination to check for reactions. As " proof " their hepatitis B vaccine is safe to be used in children, Merck & Co. stated in their 1993 product insert that " In a group of studies, 1636 doses of RECOMBIVAX HB were administered to 653 healthy infants and children (up to 10 years of age) who were monitored for 5 days after each dose. " Merck & Co. found that injection site and systemic complaints, such as fatigue and weakness, fever, headache and arthralgia (joint pain), were reported following up to 17 percent of all hepatitis B injections. Because the FDA did not require drug companies to provide scientific evidence that hepatitis B vaccine does not compromise the immune and neurological systems of children and adults over weeks, months or years post-vaccination, Merck & Co. warns in the 1996 product insert that " As with any vaccine, there is the possibility that broad use of the vaccine could reveal adverse reactions not observed in clinical trials " and Kline Beecham (1993) has a similar warning that " it is possible that expanded commercial use of the vaccine could reveal rare adverse reactions. Another warning in the Merck 1996 product insert is " it is also not known whether the vaccine can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity " and " it is not known whether the vaccine is excreted in human milk. Because many drugs are secreted in human milk, caution should be exercised when the vaccine is administered to a nursing woman. " And, although doctors routinely inject hepatitis B vaccine into children along with many other vaccines such as DPT, HIB, MMR and chicken pox vaccine, Merck & Co. state in the 1996 product insert: " Specific data are not yet available for the simultaneous administration of RECOMBIVAX HB with other vaccines. " Hep B Vaccine Efficacy Also Questioned - All vaccines stimulate only an artificial, temporary immunity, and the length of immunity conferred by the hepatitis B vaccine and the future need for more " booster " doses later in life is still not clear. Merck & Co state in their 1996 hepatitis B vaccine product insert that " the duration of the protective effect of RECOMBIVAX HB in healthy vaccinees is unknown at present and the need for booster doses is not yet defined. " In the CDC Prevention Guidelines: A Guide to Action (1997), the CDC states " The duration of protection [of hepatitis B vaccine] and need for booster doses are not yet fully defined. Between 30% and 50% of persons who develop adequate antibody after three doses of vaccine will lose detectable antibody within 7 years but protection against viremic infection and clinical disease appears to persist. " If immunity only lasts 7 years, babies vaccinated with hepatitis B vaccine may be candidates for more shots at age seven. IOM Report Reveals Lack Of Adequate Scientific Studies - In Adverse Events Associated with Childhood Vaccines published in 1994 by the Institute of Medicine, National Academy of Sciences, observations about the limitations of hepatitis B vaccine studies included the statements that " it is important to note that individual trials usually involved a few hundred subjects for study...when larger vaccination programs were monitored, observations of adverse events were necessarily less detailed and less accurately reported " and " the studies were not designed to assess serious, rare adverse events; the total number of recipients is too small and the follow-up generally too short to detect rare or delayed serious adverse reactions. " The IOM report also noted that no controlled observational studies or controlled clinical trials have ever been held to evaluate repeated reports that hepatitis B vaccine can cause Guillain-Barre syndrome; arthritis; transverse myelitis, optic neuritis, multiple sclerosis and other central demyelinating diseases of the nervous system (degeneration of the myelin sheath of the brain that helps transmit nerve impulses); or sudden infant death syndrome (SIDS). A major conclusion of the Institute of Medicine report was that almost no basic science research has been undertaken to define at the cellular and molecular level the biological mechanism of vaccine-induced injury and death. The report concluded that " The lack of adequate data regarding many of the adverse events under study was of major concern to the committee...the committee encountered many gaps and limitations in knowledge bearing directly or indirectly on the safety of vaccines. These include inadequate understanding of the biologic mechanisms underlying adverse events following natural infection or immunization, insufficient or inconsistent information from case reports and case series...and inadequate size or length of follow-up of many population-based epidemiologic studies…. " Medical Literature Cites Immune System/Brain Damage - During the past decade, there have been many reports in the medical literature (primarily in international medical journals rather than U.S. medical journals) that hepatitis B vaccination is causing chronic immune and neurological disease in children and adults, including lupus: Tudela & Bonal (1992); Mamoux & Dumont (1994); Guiserix (1996); arthritis, including polyarthritis and rheumatoid arthritis: Christan & Helin (1987); Hachulla et al (1990); on & Nye (1990); Biasi et al (1993),(1994); Vautier & Carty (1994); Hassan & Oldham (1994); Rheumatic Review (1994); Gross et al (1995); Pope et al (1995); Cathebras et al (1996); Soubrier et al (1997); Guillain Barre Syndrome GBS): Shaw et al (1988), Tuohy (1989); demyelinating disorders such as optic neuritis, Bell's Palsy, demyelinating neuropathy, transverse myelitis and multiple sclerosis: Shaw et al (1988); WHO (1990); Reutens et al (1990); Herroelen et al (1991); Nadler (1993); Brezin et al (1993); Mahassin et al (1993); Kaplanski et al (1995); Baglivo et al (1996); Marsaudon & Barrault (1996); Berkman et al (1996); Waisbren (1997); diabetes mellitus: Poutasi (1996); Classen (1996); chronic fatigue: Salit (1993); Delage et al (1993); vascular disorders: Fried et al (1987); Goolsby (1989); Cockwell et al (1990); Poullin & (1994); Mathieu et al (1996); Graniel et al (1997); and others. In 1996, Burton A. Waisbren, M.D., a cell biologist and infectious disease specialist, who is a founding member of the Infectious Disease Society of America and past President of the Infectious Disease Society of Milwaukee, pointed out in the Wisconsin Medical Journal that " there is an increasing number of reports in the refereed medical literature about demyelinizing diseases occurring after an individual has received the hepatitis B vaccination...since the hepatitis B virus itself has been reported to cause autoimmune problems, should we not be wary of giving antigens that seem to have triggered these problems? " Waisbren, in a presentation before a 1996 Institute of Medicine Vaccine Safety Forum, warned that genetically engineered hepatitis B vaccines contain polypeptide sequences that are present in human neurologic tissues such as myelin and that, by a mechanism called molecular mimicry, these polypeptides can act as autoantigens which can induce autoimmune demyelinating diseases of the brain such as multiple sclerosis. In that same year, Montinari et al published a study in Italy evaluating 30 children and adults, the majority aged 3 to 9 months, who suffered central nervous system disorders, such as seizures and autism, following hepatitis B vaccination. The purpose of the study was to investigate whether there is an immunogenetic basis (autoimmune type) responsible for the demyelination process in the brain that can occur following recombinant hepatitis B vaccination. The authors concluded " autoimmune diseases are more frequent in nations where vaccines are widely used, the so called " clear " communities " and they identified several potential genetic markers that " may visualize risk patients for autoimmune diseases following hepatitis B vaccination. Montinari's work to identify genetic factors for predisposition to hepatitis B vaccine reactions is important in light of the study in 1989 by Alper et al to identify genetic factors for those who do not respond to hepatitis B vaccination. In that study, the authors concluded that there was genetic predisposition to failure to respond to the vaccine. They stated: " These results support our hypothesis that the production of anti-HBsAg [vaccine-induced antibodies] is a dominant trait and that the inability to produce high titers of anti-HBsAG after adequate immunization is a recessive trait... " The authors concluded that the genetic markers they identified are most prevalent in caucasians of European descent " and is associated with a wide variety of diseases with autoimmune features in this population, including Type 1 diabetes mellitus... " In 1996, Barthelow Classen, M.D., CEO of Classen Immunotherapies Inc., published an epidemiologic study in the New Zealand Medical Journal and reported that there was a 60 percent increase in Type 1 diabetes (juvenile diabetes) following a massive campaign in New Zealand from 1988 to 1991 to vaccinate babies six weeks of age or older with hepatitis B vaccine. His analysis of a group of 100,000 New Zealand children prospectively followed since 1982 showed that the incidence of diabetes before the hepatitis B vaccination program began in 1988 was 11.2 cases per 100,000 children per year while the incidence of diabetes following the hepatitis B vaccination campaign was 18.2 cases per 100,000 children per year. [image] NVIC Home ©Copyright 1996-98 National Vaccine Information Center 512 W. Maple Ave., Suite 206, Vienna, VA 22180 (703) 938-DPT3 FAX: 938-5768 1-800-909-SHOT email: info@... ---------------------------------------------------------------------------- -------------------------------------------------------- Sheri Nakken, R.N., MA Vaccination Information & Choice Network, Nevada City CA http://www.nccn.net/~wwithin/vaccine.htm ANY INFO OBTAINED HERE NOT TO BE CONSTRUED AS MEDICAL OR LEGAL ADVICE. THE DECISION TO VACCINATE IS YOURS AND YOURS ALONE. Well Within's Earth Mysteries & Sacred Site Tours http://www.nccn.net/~wwithin International Tours, Homestudy Courses, ANTHRAX & OTHER Vaccine Dangers Education, Homeopathic Education KVMR Broadcaster/Programmer/Investigative Reporter, Nevada City CA CEU's for nurses, Books & Multi-Pure Water Filters Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 27, 2000 Report Share Posted July 27, 2000 " Viral hepatitis of all types is one of the easiest diseases for ascorbic acid to cure. " ---Dr Cathcart, M.D. http://www.seanet.com/~alexs/ascorbate/ Hep B Question > > > I was also send this phrase. Does it hold any merit. It is the only thing > my friend will vaccinate for: > > Hepatitis B (the > only one with an approved vaccination so far) is an untreatable viral liver > disease. There are simply no medicines with which to treat it. > > Diane > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 28, 2000 Report Share Posted July 28, 2000 I was reading that statement by Barbara Fisher( ithink) and it sums up exactly why i chose not to vaccinate. It may be 1 in however many thousands that suffer from a " severe " reaction, but i have only one Zakharia and one Elia. When i explained this to a few peds, all i got back was blank stares. Even one reaction is one too many!!! Christin Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 28, 2000 Report Share Posted July 28, 2000 At 04:36 PM 07/28/2000 EDT, you wrote: >I was reading that statement by Barbara Fisher( ithink) and it sums up >exactly why i chose not to vaccinate. It may be 1 in however many thousands >that suffer from a " severe " reaction, but i have only one Zakharia and one >Elia. When i explained this to a few peds, all i got back was blank stares. >Even one reaction is one too many!!! >Christin Read Mendelsohn's Confession of a Medical Heretic and you'll see why they give you blank stares. Disgusting! Sheri -------------------------------------------------------- Sheri Nakken, R.N., MA Vaccination Information & Choice Network, Nevada City CA http://www.nccn.net/~wwithin/vaccine.htm ANY INFO OBTAINED HERE NOT TO BE CONSTRUED AS MEDICAL OR LEGAL ADVICE. THE DECISION TO VACCINATE IS YOURS AND YOURS ALONE. Well Within's Earth Mysteries & Sacred Site Tours http://www.nccn.net/~wwithin International Tours, Homestudy Courses, ANTHRAX & OTHER Vaccine Dangers Education, Homeopathic Education KVMR Broadcaster/Programmer/Investigative Reporter, Nevada City CA CEU's for nurses, Books & Multi-Pure Water Filters Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2001 Report Share Posted May 8, 2001 Has anyone done really intensive research on the Hep B vaccine? I'd love to get some good references on it.I have a question, here's something I pulled from an article written in JAMA.. " Public health professionals counter by saying that up to 40% of hepatitis B infections come from unknown sources and that children under age 5, although a small minority of those with hepatitis B, have the greatest chance of getting chronic hepatitis B and becoming at high risk of death from cirrhosis and liver cancer. " JAMA, The Journal of the American Medical Association, July 7, 1999 v282 i1 p15 Debate Revived on Hepatitis B Vaccine Value. (Medical News & Perspectives) Marwick; Mike Mitka. I've seen this statistic before and what I want to know is HOW these children are getting Hepatitis B? Does anyone know if these is even traceable?Thanks, a, Aspiring Doula Mom to Dryden (July 17, 1997)and Niall (April 28, 2001) Wife to Randy (March 17, 2000) Learning to cloth diaper, totally breastfeeding, family bedding, researching vaccines Pacific Northwest mama. --------------------------------- Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 14, 2008 Report Share Posted April 14, 2008 France does not exist as far as the US is concerned. Nothing outside the US means anything anyway to them. They know no one can sue here, so why should they care? Sheri At 02:43 AM 4/14/2008, you wrote: I'm astounded ('tho I probably shouldn't be) that there's no discussion of changing this practice now that hep b vax manufacturers are charged with manslaughter in France for not disclosing the dangers, plus numerous civil cases. France ceased its universal hep b vax program after so many citizens became seriously ill with a variety of conditions, including MS. > > Not too cynical at all. I was told this explicitly by hospital staff when I asked this question after my last birth eight years ago. Mom's Hep B status is irrelevant unless she is planning on sharing a needle or having sex with her newborn. I refused the shot (it wasn't being offered in the years I had my first two) and in response to the quizzical look from the nurse said, " if he picks anyone up on the way home, I'll be sure he uses a condom. " > > Jake Marcus, J.D. Quote Link to comment Share on other sites More sharing options...
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