Vaccination visual chart

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The state of research in Homeopathy


TETANUS VACCINES, SPONTANEOUS ABORTIONS, & Population Control. ThinkTwice!

 

Were Tetanus Vaccines
Laced with Birth-Control Drugs?

Learn About Tetanus

more on this data http://www.thinktwice.com

During the early 1990s, the World Health Organization (WHO) had been overseeing massive vaccination campaigns against tetanus in a number of countries, among them Nicaragua, Mexico, and the Philippines. In October 1994, HLI received a communication from its Mexican affiliate, the Comite’ Pro Vida de Mexico, regarding that country’s anti-tetanus campaign. Suspicious of the campaign protocols, the Comite’ obtained several vials of the vaccine and had them analyzed by chemists. Some of the vials were found to contain human chorionic gonadotrophin (hCG), a naturally occurring hormone essential for maintaining a pregnancy.
hCG and Anti-hCG Antibodies
In nature the hCG hormone alerts the woman’s body that she is pregnant and causes the release of other hormones to prepare the uterine lining for the implantation of the fertilized egg. The rapid rise in hCG levels after conception makes it an excellent marker for confirmation of pregnancy: when a woman takes a pregnancy test she is not tested for the pregnancy itself, but for the elevated presence of hCG.
However, when introduced into the body coupled with a tetanus toxoid carrier, antibodies will be formed not only against tetanus but also against hCG. In this case the body fails to recognize hCG as a friend and will produce anti-hCG antibodies. The antibodies will attack subsequent pregnancies by killing the hCG which naturally sustains a pregnancy; when a woman has sufficient anti-hCG antibodies in her system, she is rendered incapable of maintaining a pregnancy.(1)
HLI reported the sketchy facts regarding the Mexican tetanus vaccines to its World Council members and affiliates in more than 60 countries.(2) Soon additional reports of vaccines laced with hCG hormones began to drift in from the Philippines, where more than 3.4 million women were recently vaccinated. Similar reports came from Nicaragua, which had conducted its own vaccination campaign in 1993.
The Known Factsblogphoto14
Here are the known facts concerning the tetanus vaccination campaigns in Mexico and the Philippines:
* Only women are vaccinated, and only the women between the ages of 15 and 45. (In Nicaragua the age range was 12-49.) But aren’t men at least as likely as young women to come into contact with tetanus? And what of the children? Why are they excluded?
* Human chorionic gonadotrophin (hCG) hormone has been found in the vaccines. It does not belong there — in the parlance of the O.J. Simpson murder trial, the vaccine has been “contaminated.”
* The vaccination protocols call for multiple injections — three within three months and a total of five altogether. But, since tetanus vaccinations provide protection for ten years or more, why are multiple inoculations called for?(3)
* WHO has been actively involved for more than 20 years in the development of an anti-fertility vaccine utilizing hCG tied to tetanus toxoid as a carrier — the exact same coupling as has been found in the Mexican-Philippine-Nicaragua vaccines.(4)
The Anti-Fertility Gang
Allied with the WHO in the development of an anti-fertility vaccine (AFV) using hCG with tetanus and other carriers have been UNFPA, the UN Development Programme (UNDP), the World Bank, the Population Council, the Rockefeller Foundation, the All India Institute of Medical Sciences, and a number of universities, including Uppsala, Helsinki, and Ohio State.(5) The U.S. National Institute of Child Health and Human Development (part of NIH) was the supplier of the hCG hormone in some of the AFV experiments.(6)
The WHO begain its “Special Programme” in human reproduction in 1972, and by 1993 had spent more than $356 million on “reproductive health” research.(7) It is this “Programme” which has pioneered the development of the abortificant vaccine. Over $90 million of this Programme’s funds were contributed by Sweden; Great Britain donated more than $52 million, while Norway, Denmark and Germany kicked in for $41 million , $27 million, and $12 million, respectively. The U.S., thanks to the cut-off of such funding during the Reagan-Bush administrations, has contributed “only” $5.7 million, including a new payment in 1993 by the Clinton administration of $2.5 million. Other major contibutors to the WHO Programme include UNFPA, $61 million; the World Bank, $15.5 million; the Rockefeller Foundation, $2.5 million; the Ford Foundation, over $1 million; and the IDRC (International Research and Development Centre of Canada), $716.5 thousand.
WHO and Philippine Health Department Excuses
When the first reports surfaced in the Philippines of tetanus toxoid vaccine being laced with hCG hormones, the WHO and the Philippine Department of Health (DOH) immediately denied that the vaccine contained hCG. Confronted with the results of laboratory tests which detected its presence in three of the four vials of tetanus toxoid examined, the WHO and DOH scoffed at the evidence coming from “right-to-life and Catholic” sources. Four new vials of the tetanus vaccine were submitted by DOH to St. Luke’s (Lutheran) Medical Center in Manila — and all four vials tested positive for hCG!
From outright denial the stories now shifted to the allegedly “insignificant” quantity of the hCG present; the volume of hCG present is insufficient to produce anti-hCG antibodies.
But new tests designed to detect the presence of hCG antibodies in the blood sera of women vaccinated with the tetauns toxoid vaccine were undertaken by Philippine pro-life and Catholic groups. Of thirty women tested subsequent to receiving tetanus toxoid vaccine, twenty-six tested positive for high levels of anti-hCG! If there were no hCG in the vaccine, or if it were present in only “insignificant” quantities, why were the vaccinated women found to be harboring anti-hCG antibodies? The WHO and the DOH had no answers.
New arguments surfaced: hCG’s apparent presence in the vaccine was due to “false positives” resulting from the particular substances mixed in the vaccine or in the chemicals testing for hCG. And even if hCG was really there, its presence derived from the manufacturing process.
But the finding of hCG antibodies in the blood sera of vaccinated women obviated the need to get bogged down in such debates. It was no longer necessary to argue about what may or may not have been the cause of the hCG presence, when one now had the effect of the hCG. There is no known way for the vaccinated women to have hCG antibodies in their blood unless hCG had been artificially introduced into their bodies!
Why A Tetanus Toxoid “Carrier”?
Because the human body does not attack its own naturally occurring hormone hCG, the body has to be fooled into treating hCG as an invading enemy in order to develop a successful anti-fertility vaccine utilizing hCG antibodies. A paper delivered at the 4th International Congress of Reproductive Immunology (Kiel, West Germany, 26-29 July 1989) spelled it out: “Linkage to a carrier was done to overcome the immunological tolerance to hCG.”(8)
Vaccine Untested by Drug Bureau
After the vaccine controversy had reached a fever pitch, a new bombshell exploded; none of the three different brands of tetanus vaccine being used had ever been licensed for sale and distribution or registered with the Philippine Bureau of Food and Drugs (BFAD), as required by law. The head of the BFAD lamely explained that the companies distributing these brands “did not apply for registration.”(9) The companies in question are Connaught Laboratories Ltd. and Intervex, both from Canada, and CSL Laboratories from Australia.
It seemed that the BFAD might belatedly require re-testing, but the idea was quickly rejected when the Secretary of Health declared that, since the vaccines had been certified by the WHO — there they are again! — there was assurance enough that the “vaccines come from reputable manufacturers.”(10)
Just how “reputable” one of the manufacturers might be is open to some question. In the mid-`80s Connaught Laboratories was found to be knowingly distributing vials of AIDS-contaminated blood products.(11)
Epilogue
At this juncture, evidence is beginning to appear from Africa.(12) HLI has called for a Congressional investigation of the situation, inasmuch as nearly every agency involved in the development of an anti-fertility vaccine is funded, at least in part, with U.S. monies.

 

NOTES:
(1) “Abortifacient vaccines loom as new threat,” HLI Reports, November 1993, pp. 1-2.
(2) World Council Reports, 28 November 1994, pp. 4-5.
(3) A call placed by this writer on 5 May 1995 to the Montgomery County (Maryland) Health Department, Epidemology Division — Infectious Diseases — Adult Immunizations, elicited the following information:
Q. For how long a time does the tetanus vaccination offer protection?
A. 10 years.
Q. Have you ever heard of any adult requiring three tetanus vaccinations within a 3 or 4 month time period, and a total of 5 vaccinations in all within a year or so?
A. Whaaaat! Never. No way!
Reports from the Philippines appear to confirm the 10-year immunity afforded by tetanus toxoid vaccinations: prior to the campaigns begun in 1993, the so-called booster shots were given only every 10 years.
(4) More than a score of articles, many written by WHO researchers, document WHO’s attempts to create an anti-fertility vaccine utilizing tetanus toxoid as a carrier. Some leading articles include:
“Clinical profile and Toxicology Studies on Four Women Immunized with Pr-B-hCG-TT,” Contraception, February, 1976, pp. 253-268.
“Observations on the antigenicity and clinical effects of a candidate antipregnancy vaccine: B-subunit of human chorionic gonadotropin linked to tetanus toxoid,” Fertility and Sterility, October 1980, pp. 328-335.
“Phase 1 Clinical Trials of a World Health Organisation Birth Control Vaccine,” The Lancet, 11 June 1988, pp. 1295-1298. “Vaccines for Fertility Regulation,” Chapter 11, pp. 177-198, Research in Human Reproduction, Biennial Report (1986-1987), WHO Special Programme of Research, Development and Research Training in Human Reproduction (WHO, Geneva 1988).
“Anti-hCG Vaccines are in Clinical Trials,” Scandinavian Journal of Immunology, Vol. 36, 1992, pp. 123-126.
(5) These institutional names are garnered from the journal articles cited in the previous footnote.
(6) Lancet, 11 June 1988, p. 1296.
(7) Challenges in Reproductive Health Research, Biennial Report 1992-1993, World Health Organization, Geneva, 1994, p. 186.
(8) G.P. Talwar, et al, “Prospects of an anti-hCG vaccine inducing antibodies of high affinity…(etc),” Reproductive Technology 1989, Elsevier Science Publishers, 1990, Amsterdam, New York, p. 231.
(9) “3 DOH vaccines untested by BFAD,” The Philippine Star, 4 April 1995, pp. 1, 12.
(10) “BFAD junks re-testing of controversial shot,” Manila Standard, 7 April 1995; “DOH: Toxoid vaccines are safe,” The Philippine Star, 7 April 1995.
(11) “Ottawa got blood tainted by HIV.” Ottawa Citizen, 4 April 1995.
(12) A nearly two-year old communique from Tanzania tells a familiar story: tetanus toxoid vaccinations, five in all, given only to women aged 15-45. Nigeria, too, may have been victimized; see The Lancet, 4 June 1988, p. 1273.
Credit: Copyright June/July 1995 by James A. Miller, special correspondent for Human Life International. This article was originally published in HLI Reports, Human Life International, Gaithersburg, Maryland; June/July 1995, Volume 13, Number 8. Permission to reprint granted to Thinktwice/New Atlantean Press.


DEADLY Immunity- Gov cover-up (mercury+Autism in vacc)

Deadly Immunity – Government Cover-up of a Mercury/Autism Scandal

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KEEPING UP THE PRESSURE – RFK, Jr. addressing the media during a February 15 press conference in Washington, DC on the ongoing vaccine science corruption within our government agencies. In the 12 years since the publication of “Deadly Immunity,” Mr. Kennedy has remained steadfast in his insistence that when it comes to vaccine safety and protecting the health of our children, we must do better.

by Robert F. Kennedy Jr.
World Mercury Project note: With the ongoing mainstream media blackout on questions regarding vaccine safety, we want to remind our followers of the publication–and subsequent retraction–of Robert F. Kennedy, Jr.’s 2005 article “Deadly Immunity” in Salon. The history of repression of crucial vaccine safety data runs deep. The article laid out the scientific link between thimerosal and childhood neurological disorders and published explosive excerpts from the transcripts from the CDC’s secretive June 2000 Simpsonwood conference which brought together government public health officials, vaccine manufacturers and professional medical associations. The article was groundbreaking at the time and received lots of media attention for uncovering the cozy relationship between government and industry at the expense of children’s health. Even though a dozen years have passed, the article’s facts have stood the test of time. An important read for people new to the movement and long-time advocates alike.
In June 2000, a group of top government scientists and health officials gathered for a meeting at the isolated Simpsonwood conference center in Norcross, Georgia. Convened by the Centers for Disease Control and Prevention, the meeting was held at this Methodist retreat center, nestled in wooded farmland next to the Chattahoochee River, to ensure complete secrecy. The agency had issued no public announcement of the session — only private invitations to fifty-two attendees. There were high-level officials from the CDC and the Food and Drug Administration, the top vaccine specialist from the World Health Organization in Geneva and representatives of every major vaccine manufacturer, including GlaxoSmithKline, Merck, Wyeth and Aventis Pasteur. All of the scientific data under discussion, CDC officials repeatedly reminded the participants, was strictly “embargoed.” There would be no making photocopies of documents, no taking papers with them when they left.
“I was actually stunned by what I saw,” Verstraeten told those assembled at Simpsonwood, citing the staggering number of earlier studies that indicate a link between thimerosal and speech delays, attention-deficit disorder, hyperactivity and autism.”
The federal officials and industry representatives had assembled to discuss a disturbing new study that raised alarming questions about the safety of a host of common childhood vaccines administered to infants and young children. According to a CDC epidemiologist named Tom Verstraeten, who had analyzed the agency’s massive database containing the medical records of 100,000 children, a mercury-based preservative in the vaccines — thimerosal — appeared to be responsible for a dramatic increase in autism and a host of other neurological disorders among children. “I was actually stunned by what I saw,” Verstraeten told those assembled at Simpsonwood, citing the staggering number of earlier studies that indicate a link between thimerosal and speech delays, attention-deficit disorder, hyperactivity and autism. Since 1991, when the CDC and the FDA had recommended that three additional vaccines laced with the preservative be given to extremely young infants — in one case, within hours of birth — the estimated number of cases of autism had increased fifteenfold, from one in every 2,500 children to one in 166 children.
Even for scientists and doctors accustomed to confronting issues of life and death, the findings were frightening. “You can play with this all you want,” Dr. Bill Weil, a consultant for the American Academy of Pediatrics, told the group. The results “are statistically significant.” Dr. Richard Johnston, an immunologist and pediatrician from the University of Colorado whose grandson had been born early on the morning of the meeting’s first day, was even more alarmed. “My gut feeling?” he said. “Forgive this personal comment — I do not want my grandson to get a thimerosal-containing vaccine until we know better what is going on.”
But instead of taking immediate steps to alert the public and rid the vaccine supply of thimerosal, the officials and executives at Simpsonwood spent most of the next two days discussing how to cover up the damaging data. According to transcripts obtained under the Freedom of Information Act, many at the meeting were concerned about how the damaging revelations about thimerosal would affect the vaccine industry’s bottom line. “We are in a bad position from the standpoint of defending any lawsuits,” said Dr. Robert Brent, a pediatrician at the Alfred I. duPont Hospital for Children in Delaware. “This will be a resource to our very busy plaintiff attorneys in this country.” Dr. Bob Chen, head of vaccine safety for the CDC, expressed relief that “given the sensitivity of the information, we have been able to keep it out of the hands of, let’s say, less responsible hands.” Dr. John Clements, vaccines advisor at the World Health Organization, declared that “perhaps this study should not have been done at all.” He added that “the research results have to be handled,” warning that the study “will be taken by others and will be used in other ways beyond the control of this group.”
…instead of taking immediate steps to alert the public and rid the vaccine supply of thimerosal, the officials and executives at Simpsonwood spent most of the next two days discussing how to cover up the damaging data.
In fact, the government has proved to be far more adept at handling the damage than at protecting children’s health. The CDC paid the Institute of Medicine to conduct a new study to whitewash the risks of thimerosal, ordering researchers to “rule out” the chemical’s link to autism. It withheld Verstraeten’s findings, even though they had been slated for immediate publication, and told other scientists that his original data had been “lost” and could not be replicated. And to thwart the Freedom of Information Act, it handed its giant database of vaccine records over to a private company, declaring it off-limits to researchers. By the time Verstraeten finally published his study in 2003, he had gone to work for GlaxoSmithKline and reworked his data to bury the link between thimerosal and autism.
Vaccine manufacturers had already begun to phase thimerosal out of injections given to American infants — but they continued to sell off their mercury-based supplies of vaccines until last year. The CDC and FDA gave them a hand, buying up the tainted vaccines for export to developing countries and allowing drug companies to continue using the preservative in some American vaccines — including several pediatric flu shots as well as tetanus boosters routinely given to eleven-year-olds.
The drug companies are also getting help from powerful lawmakers in Washington. Senate Majority Leader Bill Frist, who has received $873,000 in contributions from the pharmaceutical industry, has been working to immunize vaccine makers from liability in 4,200 lawsuits that have been filed by the parents of injured children. On five separate occasions, Frist has tried to seal all of the government’s vaccine-related documents — including the Simpsonwood transcripts — and shield Eli Lilly, the developer of thimerosal, from subpoenas. In 2002, the day after Frist quietly slipped a rider known as the “Eli Lilly Protection Act” into a homeland security bill, the company contributed $10,000 to his campaign and bought 5,000 copies of his book on bioterrorism. The measure was repealed by Congress in 2003 — but earlier this year, Frist slipped another provision into an anti-terrorism bill that would deny compensation to children suffering from vaccine-related brain disorders. “The lawsuits are of such magnitude that they could put vaccine producers out of business and limit our capacity to deal with a biological attack by terrorists,” says Dean Rosen, health policy adviser to Frist.
Even many conservatives are shocked by the government’s effort to cover up the dangers of thimerosal. Rep. Dan Burton, a Republican from Indiana, oversaw a three-year investigation of thimerosal after his grandson was diagnosed with autism. “Thimerosal used as a preservative in vaccines is directly related to the autism epidemic,” his House Government Reform Committee concluded in its final report. “This epidemic in all probability may have been prevented or curtailed had the FDA not been asleep at the switch regarding a lack of safety data regarding injected thimerosal, a known neurotoxin.” The FDA and other public-health agencies failed to act, the committee added, out of “institutional malfeasance for self protection” and “misplaced protectionism of the pharmaceutical industry.”
The story of how government health agencies colluded with Big Pharma to hide the risks of thimerosal from the public is a chilling case study of institutional arrogance, power and greed. I was drawn into the controversy only reluctantly. As an attorney and environmentalist who has spent years working on issues of mercury toxicity, I frequently met mothers of autistic children who were absolutely convinced that their kids had been injured by vaccines. Privately, I was skeptical.
I doubted that autism could be blamed on a single source, and I certainly understood the government’s need to reassure parents that vaccinations are safe; the eradication of deadly childhood diseases depends on it. I tended to agree with skeptics like Rep. Henry Waxman, a Democrat from California, who criticized his colleagues on the House Government Reform Committee for leaping to conclusions about autism and vaccinations. “Why should we scare people about immunization,” Waxman pointed out at one hearing, “until we know the facts?”
It was only after reading the Simpsonwood transcripts, studying the leading scientific research and talking with many of the nation’s pre-eminent authorities on mercury that I became convinced that the link between thimerosal and the epidemic of childhood neurological disorders is real. Five of my own children are members of the Thimerosal Generation — those born between 1989 and 2003 — who received heavy doses of mercury from vaccines. “The elementary grades are overwhelmed with children who have symptoms of neurological or immune-system damage,” Patti White, a school nurse, told the House Government Reform Committee in 1999. “Vaccines are supposed to be making us healthier; however, in twenty-five years of nursing I have never seen so many damaged, sick kids. Something very, very wrong is happening to our children.”
“Vaccines are supposed to be making us healthier; however, in twenty-five years of nursing I have never seen so many damaged, sick kids. Something very, very wrong is happening to our children.”
More than 500,000 kids currently suffer from autism, and pediatricians diagnose more than 40,000 new cases every year. The disease was unknown until 1943, when it was identified and diagnosed among eleven children born in the months after thimerosal was first added to baby vaccines in 1931.
Some skeptics dispute that the rise in autism is caused by thimerosal-tainted vaccinations. They argue that the increase is a result of better diagnosis — a theory that seems questionable at best, given that most of the new cases of autism are clustered within a single generation of children. “If the epidemic is truly an artifact of poor diagnosis,” scoffs Dr. Boyd Haley, one of the world’s authorities on mercury toxicity, “then where are all the twenty-year-old autistics?” Other researchers point out that Americans are exposed to a greater cumulative “load” of mercury than ever before, from contaminated fish to dental fillings, and suggest that thimerosal in vaccines may be only part of a much larger problem. It’s a concern that certainly deserves far more attention than it has received — but it overlooks the fact that the mercury concentrations in vaccines dwarf other sources of exposure to our children.
What is most striking is the lengths to which many of the leading detectives have gone to ignore — and cover up — the evidence against thimerosal. From the very beginning, the scientific case against the mercury additive has been overwhelming. The preservative, which is used to stem fungi and bacterial growth in vaccines, contains ethylmercury, a potent neurotoxin. Truckloads of studies have shown that mercury tends to accumulate in the brains of primates and other animals after they are injected with vaccines — and that the developing brains of infants are particularly susceptible. In 1977, a Russian study found that adults exposed to much lower concentrations of ethylmercury than those given to American children still suffered brain damage years later. Russia banned thimerosal from children’s vaccines twenty years ago, and Denmark, Austria, Japan, Great Britain and all the Scandinavian countries have since followed suit.
You couldn’t even construct a study that shows thimerosal is safe,” says Haley, who heads the chemistry department at the University of Kentucky. “It’s just too darn toxic. If you inject thimerosal into an animal, its brain will sicken. If you apply it to living tissue, the cells die. If you put it in a petri dish, the culture dies. Knowing these things, it would be shocking if one could inject it into an infant without causing damage.”
Internal documents reveal that Eli Lilly, which first developed thimerosal, knew from the start that its product could cause damage — and even death — in both animals and humans. In 1930, the company tested thimerosal by administering it to twenty-two patients with terminal meningitis, all of whom died within weeks of being injected — a fact Lilly didn’t bother to report in its study declaring thimerosal safe. In 1935, researchers at another vaccine manufacturer, Pittman-Moore, warned Lilly that its claims about thimerosal’s safety “did not check with ours.” Half the dogs Pittman injected with thimerosal-based vaccines became sick, leading researchers there to declare the preservative “unsatisfactory as a serum intended for use on dogs.”
In the decades that followed, the evidence against thimerosal continued to mount. During the Second World War, when the Department of Defense used the preservative in vaccines on soldiers, it required Lilly to label it “poison.” In 1967, a study in Applied Microbiology found that thimerosal killed mice when added to injected vaccines. Four years later, Lilly’s own studies discerned that thimerosal was “toxic to tissue cells” in concentrations as low as one part per million — 100 times weaker than the concentration in a typical vaccine. Even so, the company continued to promote thimerosal as “nontoxic” and also incorporated it into topical disinfectants. In 1977, ten babies at a Toronto hospital died when an antiseptic preserved with thimerosal was dabbed onto their umbilical cords.
Internal documents reveal that Eli Lilly, which first developed thimerosal, knew from the start that its product could cause damage — and even death — in both animals and humans.
In 1982, the FDA proposed a ban on over-the-counter products that contained thimerosal, and in 1991 the agency considered banning it from animal vaccines. But tragically, that same year, the CDC recommended that infants be injected with a series of mercury-laced vaccines. Newborns would be vaccinated for hepatitis B within twenty-four hours of birth, and two-month-old infants would be immunized for haemophilus influenzae B and diphtheria-tetanus-pertussis.
The drug industry knew the additional vaccines posed a danger. The same year that the CDC approved the new vaccines, Dr. Maurice Hilleman, one of the fathers of Merck’s vaccine programs, warned the company that six-month-olds who were administered the shots would suffer dangerous exposure to mercury. He recommended that thimerosal be discontinued, “especially when used on infants and children,” noting that the industry knew of nontoxic alternatives. “The best way to go,” he added, “is to switch to dispensing the actual vaccines without adding preservatives.”
For Merck and other drug companies, however, the obstacle was money. Thimerosal enables the pharmaceutical industry to package vaccines in vials that contain multiple doses, which require additional protection because they are more easily contaminated by multiple needle entries. The larger vials cost half as much to produce as smaller, single-dose vials, making it cheaper for international agencies to distribute them to impoverished regions at risk of epidemics. Faced with this “cost consideration,” Merck ignored Hilleman’s warnings, and government officials continued to push more and more thimerosal-based vaccines for children. Before 1989, American preschoolers received eleven vaccinations — for polio, diphtheria-tetanus-pertussis and measles-mumps-rubella. A decade later, thanks to federal recommendations, children were receiving a total of twenty-two immunizations by the time they reached first grade.
As the number of vaccines increased, the rate of autism among children exploded. During the 1990s, 40 million children were injected with thimerosal-based vaccines, receiving unprecedented levels of mercury during a period critical for brain development. Despite the well-documented dangers of thimerosal, it appears that no one bothered to add up the cumulative dose of mercury that children would receive from the mandated vaccines. “What took the FDA so long to do the calculations?” Peter Patriarca, director of viral products for the agency, asked in an e-mail to the CDC in 1999. “Why didn’t CDC and the advisory bodies do these calculations when they rapidly expanded the childhood immunization schedule?”
But by that time, the damage was done. At two months, when the infant brain is still at a critical stage of development, infants routinely received three inoculations that contained a total of 62.5 micrograms of ethylmercury — a level 99 times greater than the EPA’s limit for daily exposure to methylmercury, a related neurotoxin. Although the vaccine industry insists that ethylmercury poses little danger because it breaks down rapidly and is removed by the body, several studies — including one published in April by the National Institutes of Health — suggest that ethylmercury is actually more toxic to developing brains and stays in the brain longer than methylmercury.
Officials responsible for childhood immunizations insist that the additional vaccines were necessary to protect infants from disease and that thimerosal is still essential in developing nations, which, they often claim, cannot afford the single-dose vials that don’t require a preservative. Dr. Paul Offit, one of CDC’s top vaccine advisers, told me, “I think if we really have an influenza pandemic — and certainly we will in the next twenty years, because we always do — there’s no way on God’s earth that we immunize 280 million people with single-dose vials. There has to be multidose vials.”
But while public-health officials may have been well-intentioned, many of those on the CDC advisory committee who backed the additional vaccines had close ties to the industry. Dr. Sam Katz, the committee’s chair, was a paid consultant for most of the major vaccine makers and was part of a team that developed the measles vaccine and brought it to licensure in 1963. Dr. Neal Halsey, another committee member, worked as a researcher for the vaccine companies and received honoraria from Abbott Labs for his research on the hepatitis B vaccine.
Indeed, in the tight circle of scientists who work on vaccines, such conflicts of interest are common. Rep. Burton says that the CDC “routinely allows scientists with blatant conflicts of interest to serve on intellectual advisory committees that make recommendations on new vaccines,” even though they have “interests in the products and companies for which they are supposed to be providing unbiased oversight.” The House Government Reform Committee discovered that four of the eight CDC advisers who approved guidelines for a rotavirus vaccine “had financial ties to the pharmaceutical companies that were developing different versions of the vaccine.”
Offit, who shares a patent on one of the vaccines, acknowledged to me that he “would make money” if his vote eventually leads to a marketable product. But he dismissed my suggestion that a scientist’s direct financial stake in CDC approval might bias his judgment. “It provides no conflict for me,” he insists. “I have simply been informed by the process, not corrupted by it. When I sat around that table, my sole intent was trying to make recommendations that best benefited the children in this country. It’s offensive to say that physicians and public-health people are in the pocket of industry and thus are making decisions that they know are unsafe for children. It’s just not the way it works.”
Other vaccine scientists and regulators gave me similar assurances. Like Offit, they view themselves as enlightened guardians of children’s health, proud of their “partnerships” with pharmaceutical companies, immune to the seductions of personal profit, besieged by irrational activists whose anti-vaccine campaigns are endangering children’s health. They are often resentful of questioning. “Science,” says Offit, “is best left to scientists.”
Still, some government officials were alarmed by the apparent conflicts of interest. In his e-mail to CDC administrators in 1999, Paul Patriarca of the FDA blasted federal regulators for failing to adequately scrutinize the danger posed by the added baby vaccines. “I’m not sure there will be an easy way out of the potential perception that the FDA, CDC and immunization-policy bodies may have been asleep at the switch re: thimerosal until now,” Patriarca wrote. The close ties between regulatory officials and the pharmaceutical industry, he added, “will also raise questions about various advisory bodies regarding aggressive recommendations for use” of thimerosal in child vaccines.
If federal regulators and government scientists failed to grasp the potential risks of thimerosal over the years, no one could claim ignorance after the secret meeting at Simpsonwood. But rather than conduct more studies to test the link to autism and other forms of brain damage, the CDC placed politics over science. The agency turned its database on childhood vaccines — which had been developed largely at taxpayer expense — over to a private agency, America’s Health Insurance Plans, ensuring that it could not be used for additional research. It also instructed the Institute of Medicine, an advisory organization that is part of the National Academy of Sciences, to produce a study debunking the link between thimerosal and brain disorders. The CDC “wants us to declare, well, that these things are pretty safe,” Dr. Marie McCormick, who chaired the IOM’s Immunization Safety Review Committee, told her fellow researchers when they first met in January 2001. “We are not ever going to come down that [autism] is a true side effect” of thimerosal exposure. According to transcripts of the meeting, the committee’s chief staffer, Kathleen Stratton, predicted that the IOM would conclude that the evidence was “inadequate to accept or reject a causal relation” between thimerosal and autism. That, she added, was the result “Walt wants” — a reference to Dr. Walter Orenstein, director of the National Immunization Program for the CDC.
For those who had devoted their lives to promoting vaccination, the revelations about thimerosal threatened to undermine everything they had worked for. “We’ve got a dragon by the tail here,” said Dr. Michael Kaback, another committee member. “The more negative that [our] presentation is, the less likely people are to use vaccination, immunization — and we know what the results of that will be. We are kind of caught in a trap. How we work our way out of the trap, I think is the charge.”
Even in public, federal officials made it clear that their primary goal in studying thimerosal was to dispel doubts about vaccines. “Four current studies are taking place to rule out the proposed link between autism and thimerosal,” Dr. Gordon Douglas, then-director of strategic planning for vaccine research at the National Institutes of Health, assured a Princeton University gathering in May 2001. “In order to undo the harmful effects of research claiming to link the [measles] vaccine to an elevated risk of autism, we need to conduct and publicize additional studies to assure parents of safety.” Douglas formerly served as president of vaccinations for Merck, where he ignored warnings about thimerosal’s risks.
In May of last year (2004), the Institute of Medicine issued its final report. Its conclusion: There is no proven link between autism and thimerosal in vaccines. Rather than reviewing the large body of literature describing the toxicity of thimerosal, the report relied on four disastrously flawed epidemiological studies examining European countries, where children received much smaller doses of thimerosal than American kids. It also cited a new version of the Verstraeten study, published in the journal Pediatrics, that had been reworked to reduce the link between thimerosal and autism. The new study included children too young to have been diagnosed with autism and overlooked others who showed signs of the disease. The IOM declared the case closed and — in a startling position for a scientific body — recommended that no further research be conducted.
The report may have satisfied the CDC, but it convinced no one. Rep. David Weldon, a Republican physician from Florida who serves on the House Government Reform Committee, attacked the Institute of Medicine, saying it relied on a handful of studies that were “fatally flawed” by “poor design” and failed to represent “all the available scientific and medical research.” CDC officials are not interested in an honest search for the truth, Weldon told me, because “an association between vaccines and autism would force them to admit that their policies irreparably damaged thousands of children. Who would want to make that conclusion about themselves?”
Under pressure from Congress and parents, the Institute of Medicine convened another panel to address continuing concerns about the Vaccine Safety Datalink Data Sharing program. In February, the new panel, composed of different scientists, criticized the way the VSD had been used in the Verstraeten study, and urged the CDC to make its vaccine database available to the public.
So far, though, only two scientists have managed to gain access. Dr. Mark Geier, president of the Genetics Center of America, and his son, David, spent a year battling to obtain the medical records from the CDC. Since August 2002, when members of Congress pressured the agency to turn over the data, the Geiers have completed six studies that demonstrate a powerful correlation between thimerosal and neurological damage in children. One study, which compares the cumulative dose of mercury received by children born between 1981 and 1985 with those born between 1990 and 1996, found a “very significant relationship” between autism and vaccines. Another study of educational performance found that kids who received higher doses of thimerosal in vaccines were nearly three times as likely to be diagnosed with autism and more than three times as likely to suffer from speech disorders and mental retardation. Another soon-to-be published study shows that autism rates are in decline following the recent elimination of thimerosal from most vaccines.
As the federal government worked to prevent scientists from studying vaccines, others have stepped in to study the link to autism. In April, reporter Dan Olmsted of UPI undertook one of the more interesting studies himself. Searching for children who had not been exposed to mercury in vaccines — the kind of population that scientists typically use as a “control” in experiments — Olmsted scoured the Amish of Lancaster County, Pennsylvania, who refuse to immunize their infants. Given the national rate of autism, Olmsted calculated that there should be 130 autistics among the Amish. He found only four. One had been exposed to high levels of mercury from a power plant. The other three — including one child adopted from outside the Amish community — had received their vaccines.
At the state level, many officials have also conducted in-depth reviews of thimerosal. While the Institute of Medicine was busy whitewashing the risks, the Iowa legislature was carefully combing through all of the available scientific and biological data. “After three years of review, I became convinced there was sufficient credible research to show a link between mercury and the increased incidences in autism,” says state Sen. Ken Veenstra, a Republican who oversaw the investigation. “The fact that Iowa’s 700 percent increase in autism began in the 1990s, right after more and more vaccines were added to the children’s vaccine schedules, is solid evidence alone.” Last year, Iowa became the first state to ban mercury in vaccines, followed by California. Similar bans are now under consideration in thirty-two other states.
But instead of following suit, the FDA continues to allow manufacturers to include thimerosal in scores of over-the-counter medications as well as steroids and injected collagen. Even more alarming, the government continues to ship vaccines preserved with thimerosal to developing countries — some of which are now experiencing a sudden explosion in autism rates. In China, where the disease was virtually unknown prior to the introduction of thimerosal by U.S. drug manufacturers in 1999, news reports indicate that there are now more than 1.8 million autistics. Although reliable numbers are hard to come by, autistic disorders also appear to be soaring in India, Argentina, Nicaragua and other developing countries that are now using thimerosal-laced vaccines. The World Health Organization continues to insist thimerosal is safe, but it promises to keep the possibility that it is linked to neurological disorders “under review.”
I devoted time to study this issue because I believe that this is a moral crisis that must be addressed. If, as the evidence suggests, our public-health authorities knowingly allowed the pharmaceutical industry to poison an entire generation of American children, their actions arguably constitute one of the biggest scandals in the annals of American medicine. “The CDC is guilty of incompetence and gross negligence,” says Mark Blaxill, vice president of Safe Minds, a nonprofit organization concerned about the role of mercury in medicines. “The damage caused by vaccine exposure is massive. It’s bigger than asbestos, bigger than tobacco, bigger than anything you’ve ever seen.”
It’s hard to calculate the damage to our country — and to the international efforts to eradicate epidemic diseases — if Third World nations come to believe that America’s most heralded foreign-aid initiative is poisoning their children. It’s not difficult to predict how this scenario will be interpreted by America’s enemies abroad. The scientists and researchers — many of them sincere, even idealistic — who are participating in efforts to hide the science on thimerosal claim that they are trying to advance the lofty goal of protecting children in developing nations from disease pandemics. They are badly misguided. Their failure to come clean on thimerosal will come back horribly to haunt our country and the world’s poorest populations.
If, as the evidence suggests, our public-health authorities knowingly allowed the pharmaceutical industry to poison an entire generation of American children, their actions arguably constitute one of the biggest scandals in the annals of American medicine.
###
After several revisions to the article and nearly 6 years after the original publication date, Salon.com retracted the article from its website archives without consideration or opportunity for rebuttal. For the reasons behind why Salon.com pulled the article, click here.
“Deadly Immunity” was simultaneously published in Rolling Stone Magazine (www.RollingStone.com) on July 14, 2005 and can be read on their website with a Rolling Stone Magazine subscription.
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Addiction to pain meds responded well to homeopathic Morphinum

Original article found at http://www.Hpathy.com
Homeopath Katharina Riedener presents a case of addiction to painkillers that responded to Morphinum.

Visit Jan. 11.2011
Male 47,homeopathics6
Oct. 09 was admitted to hospital with severe abdominal cramps, 3 feet of his small intestines had died off because of a congested vein and were removed.
Colostomy until April 2010, Total Parenteral Nutrition.
Removal of gallstones June 2010 (side effect of TPN), gall bladder is fine.
Between Jan. and March 2010 had 2 bouts of Septicemia and Hematoma on upper thighs, which required hospitalization.
Current meds: Warfarin, Pepsin and Acidopholus to aid digestion.
Since release from hospital after intestine was removed patient has been on Fentanyl patch:
Fentanyl is approximately 100 times more potent than Morphine with 100 micrograms of fentanyl approximately equivalent to 10 mg of morphine and 75 mg of Pethidine (meperidine) in analgesic activity.
Current dosage 12 mcg/h –  lowest dosage available
Patient:
One patch is supposed to last 72 hours but after 48 hours I have severe withdrawal symptoms and need another patch. Even though I use it after 48 hours it means a sleepless night in agony. Patient describes himself as being an introverted hard working person. He has been healthy all of his life, is happily married with 2 boys. I never tried drugs in my life! There was no reason for the blood clot that could be found. I felt healthy until shortly before, then I had some abdominal complaints, kind of flu like. I haven’t had any pain since June 2010 and only use the patch because I am addicted to it. I tried to get off the patch, they gave large amounts of Oxycondone, when the withdrawal symptoms come I take them but they don’t really work. They continue to prescribe the Fentanyl patch because of my addiction.  One time I lost a patch at lunch time. At night I couldn’t handle it anymore, went to the hospital and they gave me a Morphine injection.
Presenting symptoms:Featured Image -- 2252
Cannot relax, lower legs are constantly moving, trembling. Feel like I want to throw my arms around, extremely restless, cannot concentrate on reading or anything. I take everything very personally, things that normally don’t bother me, I become obsessed with. I will say things that I regret minutes later, very impulsive, up and down all the time.  A simple thing I cannot let go, worry about everything for hours, even if it is the most common task. I feel like I am in a constant defensive attack. It is impossible to sleep, and if I do sleep it is very restless with terrible dreams. In the dreams, everything is dirty and disgusting, dog shit everywhere and I step into it. I am not actually active in the dream it is the surroundings that are very disgusting,  I had these dreams when I was on high doses of Morphine in the hospital.
I have memory gaps, for days sometimes I don’t remember what I did. The day I lost the patch had hallucinations of a road worker with a shovel he was in front of the car. My eyes are very sore when on withdrawal, strange sensation almost like a headache. Temperature fluctuations: I feel hot and cold with shivering and perspiration when hot. I can manage a day at work, then I am done, I cannot do anything else. My bowels work normal.  I am sensitive to onions, garlic and cabbage now, which I never used to before. I snore extremely since on the patch.
Neither Fentanil nor Oxycondone are available as homeopathic remedies. The closest homeopathic remedy available is Morphinum. The patient feels like a drug addict, the effect of the drugs and the addiction is what needs to be treated in this case. I looked at this as an acute situation rather than trying to find a constitutional remedy.
Rubrics:
Generalities: CRAMPS: MUSCLES: CONVULSIVE, SPASMODIC, INTERRUPTING SLEEP
Irritability: physical, excessive
Heat: flushes of: alternating with: chills
Mind:
Excitement, excitable: trifles, over
irritability: general.
Morose, sulky, cross, fretful, ill-humor, peevish.
Sensitive, oversensitive: general
Suspiciousness, mistrustfulness
Anger, irascibility: trifles, at
Hallucinations for many days (Allen)
Memory, weakness, loss of
Eyes:
Fullness
Sleep:
Very restless, no sleep all night (Allen)
Feb. 8.11:
Presc. Morphinum LM 5, 4 drops daily, 10 succ. Repeat 2 -3 x if withdrawal symptoms kick in.
Feb.15.11: ( 1 week)
Still have about 75 % of the withdrawal symptoms, sleeping a bit better, now go to sleep about midnight; before it was 3 a.m.
My moods are not quite as aggressive.
Eye pressure is gone
More tired in general
Still on patch every 2. Day
Morph. LM 5, 6 drops 15 succ. Regular days, 8 drops 15 succ. Withdrawal days.
Feb. 24.11:
Still problems with sleeping when the patch is changing, not as extreme as before, manage to stay in bed, doesn’t drive me up the walls anymore. Moods the same, but I do feel better inside, don’t have such obsessive thoughts anymore. I feel very positive there has been a definite change in 2 weeks.  No more temperature fluctuations. Eyes are fine
LM 5 10/12 drops 15 succ.
March 15 11:
A lot less withdrawal symptoms, sleeping a lot more now. Restless legs are much better. I had my last patch 5 days ago, Oxycontin 20 mg. Every 12 hours instead.
(Patient decided to cut them in half and only every 24 hrs). After 3 days the withdrawal symptoms (restless legs only) started to come back, I took 12 drops of the remedy and had no problems after that, then took nothing again for 24 hrs. I am very happy and excited about this progress; it has been absolutely amazing for me. I am in the best shape since a long time.
LM 5 10/12 drops 20 succ.
March 24.11:
(GP prescribed Oxycontin 10 mg, patient cuts them in half. 2 x a day)
Still progressing well, sleeping well. I am really happy to have a life again, after work enjoy my relaxing time. Feel better overall less tired. Moods are better, nicer again, family says there is huge improvement. Few obsessive thoughts still but much less. No more weird dreams
LM 8, 5 drops, 10 succ.
April 12.11:
Oxyc. 5 mg now, cut in half, 2 x a day, LM 8, 8 drops, 15 succ.
April 28.11:
Had a couple of days with withdrawal after switching to 5 mg. But now back to feeling good.
May 12.11:
Oxyc. 2.5 mg 2 x a day
LM 9, 5 drops 10 succ.
June 15.11:
Some withdrawals symptoms after cutting Oxyc. In half
LM 9, 8 drops, 10 succ. Feeling good overall, energy levels about 70 % from before surgery
July 8.11:
Hospitalized with kidney colic from kidney stones.
Unfortunately patient didn’t not get in touch with me. They gave me pain killers. They didn’t work so they put me on Morphine for 3 days! Home after 4 days still sever pains, needed more Morphine, patient is discouraged because of returning withdrawal symptoms.
Back on Oxycontin 5 mg twice a day
Morph. LM 9 8 drops 10 succ. Twice a day
Aug. 11.11:
I haven’t been able to reduce Oxycontin, still sleeping well but bad moods and some restlessness have come back.
LM 9 10 drops, 15 succ.
Oct. 11.11:
Had 2 bouts of kidney stones and gall stones again too, bladder infection and prostate infection. Anti-biotic treatment and also Morphine again in the hospital 5 mg a day.
LM 10, 5 drops 10 succ. 2 – 3 a day
Oct. 17.11:
Kidney/ Bladder colic’s are back, this time patient does not go to the hospital and instead contacts me.
Presenting Symtpoms:
Kidney, pain extending, testes to
Kidney, pain extending, thighs to
Kidney, pain, colic left
Kidney, pain urination, agg. Before
Kidney, pain, region of
Bladder, pain burning
Bladder, urging to urinate, morbid desire
Bladder, pain, urinating before
Urethra, pain, urination before
Presc. Berberis 200 C
Oct. 18.11:
Pain in kidney and bladder almost all gone. Patient decides to stop taking Warfarin,
Berberis 6 CH daily.
Nov. 8.11:
No more kidney/bladder problems
Oxycontin 5 mg a day
Morph. LM 10, 10 drops, 10 succ.
Dec. 13.11:
Feeling quite well. Will try and reduce Oxycontin again
Morph LM 11, 5 drops 10 succ.
Feb. 14.12:
Jan. 19.12 I stopped taking the Oxycontin, continued the remedy for another 7 days and then stopped that too. Had a couple of nights where I felt funny but then I was fine. Occasionally I have a few seconds where I feel like I am on withdrawal but it passes quickly. No more kidney or bladder problems.  Feeling very good emotionally as well as physically still get tired sometimes. Food sensitivities are much better too.
Plan: wait and look at a constitutional remedy in about 2 months.


Joint pain and homeopathy

Cranky, achy joints are a common complaint in America. In fact, according to the Centers for Disease Control, 50% of all adults will complain of things like a sore knee or sore hip by age 85.
What do we mean by joint pain or simple arthritic pain? The typical symptoms include pain of various descriptions that is often accompanied by stiffness and possibly a bit of swelling around the sore joint.
If you are someone who suffers with simple arthritic pain, it may be comforting to know that homeopathy can help. In fact, here are a few of the remedies often used for acute episodes of discomfort:
Arsenicum album: Someone needing this remedy would find their pain much worse after midnight and from 1-2:00AM. This peculiar characteristic is one of the keys to choosing Arsenicum for almost any ailment. An Arsenicum patient is also intensely restless (both mentally and physically), anxious and often feels exhausted.

Bryonia: A person needing this homeopathic remedy is fairly easy to spot. For almost any ailment, a Bryonia patient is worse from the slightest movement and feels better when they keep perfectly still. They tend to be worse from cold, dry weather and they also tend to be irritable and desire solitude with their complaint. The pains tend to be of a stitching nature. The joints affected can also feel a bit warm to the touch. These folks tend to be thirsty for large quantities of fluid at intervals and can suffer with constipation that includes hard, burnt looking stools. They may also be a bit better from perspiration.

Ledum: A person needing this homeopathic remedy will find the joint that is sore is cold to the touch but feels better from cold applications rather than warm ones. Despite being generally chilly by nature, they are also generally worse from warmth – including the warmth of the bed. Motion of any kind makes the joint pain worse – and jarring the joint can cause great pain. A Ledum joint is often a bit bloated and discolored.

Pulsatilla: Someone needing this homeopathic remedy is again a bit easy to spot. With simple arthritic pain – the pain seems to shift rapidly from part to part and can be intense one minute and mild the next. The symptoms are very changeable. The joints can be a bit red and swollen as well. The pains can be of a tearing or drawing nature that are a bit better from motion and after motion. The pains are typically worse in a warm room and better from cold applications. A sense of chilliness increases with the pain and yet, as I mentioned above, they are worse from heat of any kind – particularly at night in bed. They often feel better uncovering, from cool open air and in some cases from cold drinks. They are also sensitive to being jostled or jarred and to touch or pressure. Another key indication for Pulsatilla – the patient cannot talk about their symptoms without weeping – and in general – they tend to be thirstless.

Rhus toxicodendron: The person needing this homeopathic remedy presents with fairly clear characteristic symptoms. They tend to have pain that is aggravated on beginning to move – the pain gets better during motion. They are also better from warmth and aggravated during change of position though changing position gives temporary relief. These folks are very definitely aggravated by cold, wet weather and worse from cold air and cold applications. The pains tend to be drawing, pulling, contractive, sore – at times the pain causes the patient to feel weakness in the joint. Joints may even feel a bit sprained. Rhus tox patients tends to be a bit sad and anxious – somewhat like Arsenicum, also a chilly remedy. Symptoms tend to be worse late at night and towards morning. What is the absolutely critical symptom of Rhus tox?? The Rhus tox patient has to be affected by weather… if you or your patient are not affected by the weather – you probably need to seek a different remedy.

Once you have chosen a remedy that appears to match your symptoms (remember – homeopathy is individualized medicine – the remedy you need must match your symptom profile) dose with either a 30C or 200C potency to start – placing one pellet under the tongue or one pellet in water, stirring vigorously and taking teaspoon doses as needed. Always cease dosing when relief begins and only redose if symptoms again worsen. As with any medical condition, consult with your physician if you have any concerns about the severity of your problem as it may first require medical diagnosis and/or intervention and monitoring. Article by dr. Lisa Samet ND


Homeopathy for Sweating

Posted by Amit Karkare

 

image
Radhika came to my clinic for the complaints of excessive sweating of palms and soles. She almost used to have cold clammy palms throughout the day, more pronounced while she studied for her exams. She had stopped using an ink-pen since the sweating used to bloat the writing. She had hyperhydrosis. It is a condition that leads to excessive sweating – either on the entire body or on specific parts.
It was very embarrassing for her to shake hands with anybody since the immediate reaction from the opposite person used to be removing the hand as early as possible and wiping it. She had marked chilly response to the environment, fanning and would need more woolen garments than her friends. She was prescribed Silica in infrequent doses [weekly one dose]. Within two months, her perspiration reduced significantly and she could perform her daily chores without any discomfort.
Homeopathy has always proved itself as the best therapy for hyperhydrosis. Modern medicine does not have anything to offer to these patients. Homeopathy treats this complaint as a dispositional derangement. Thus assessing the emotional – intellectual – physical composition of the individual to select a suitable constitutional remedy is the key to success.
To aid this, here are the indications of few prominent remedies that cover excessive sweating as a symptom. To help locating an individual remedy I have italicized their names:
The patient of calcarea carb constitution sweats profusely while sleeping – almost wetting the pillow, like the patients of silica or sanicula. There is also perspiration on the back of the head, neck and chest. Mostly sweats in the upper part of the body. The sweat has a sour smell and the sweating is more during sleep. Conium also sweats more during sleep; almost as soon as one sleeps or even when closes eyes to sleep. Exactly opposite is seen in Sambucus – where there is a profuse sweat over the entire body during waking hours, while on going to sleep, the dry heat returns.
If calcarea sweat smells sour, the sweating of Bovista smells like an onion. Offensive sweating is a characteristic of many remedies including Alumina, Graphites, Psorinum, Phosporus, Sanicula, Thuja and their leader Silica. Among these, phosphorus sweat has the odor of sulphur fumes, while thuja smells like honey. Most of these also show a tendency to sweat more on palms and soles.
If we are discussing the smell of the perspiration, the taste should not be left un-noted. The remedy Caladium has a unique quality – the sweating of this remedy is sweet in taste, so much that it can even attract flies. It has got yet another characteristic – the patient of caladium sweats profusely after any acute diseases, so distinctly that we can even say that the profuse sweat relieves all sufferings in caladium [also in Natrum mur].
Thuja shows sweating only on uncovered parts, or all over except the head. These patients also sweat a lot of sour smelling or fetid sweat during sleep.
The prominent remedy for cholera, Veratrum album has cold perspiration on the forehead with nearly all complaints. Tabacum has it all over the body.
Isn’t it interesting to know the various characteristic features that a remedy can throw just in the pattern of sweating? Knowing all this will not only improve our remedy selection but also our case-taking. We would only ask those questions, whose probable answers we expect already.


Nerves/Anxiety and Homeopathics

EXAM NERVES HOMEOPATHIC REMEDIES blogphoto2

All these remedies have ‘anticipatory anxiety’

Aconite: Acute waves of fear or panic, coming suddenly. Agitation, restlessness and fear, may even think they are about to die (a common feeling in panic attacks so use a brown paper bag or Buteyko breathing to balance your CO2 ).
Other symptoms may include: dry skin and mouth; thirst; pounding heart. Aconite can also treat ongoing anxiety caused by a past traumatic event.

Aethusia cynapium: brain fatigue from over-study. Foggy head and inability to think and to fix attention. Examination fears.

Ambra grisea: forgetful, confused, hopeless, no confidence. Shy and easily embarrassed. Dread performing in front of others.

Anacardium: Nervous exhaustion from over-study. Fear of examinations with lack of confidence. Great difficulty remembering what they have revised, and completely lose their confidence. So great is their psycological disturbance due to the stress of possible failure, that they may feel suicidal.

Argentum nitricum: Arg nit can appear like a headless chicken! Agitated, impulsive, talkative, speedy. Worrying ‘what if?’, worrying about missing deadlines, being late, appearing in public, failure.
Other symptoms may include: craving sweets but feel worse after eating them. Vomiting or diarrhoea and trembling, feel hot.

Arsenicum: anxious, panicky, restless, full of dread, cannot bear to be alone. Perfectionists or high achievers who want everything ‘just so’. Worse at night, worse after midnight.
is good for people who feel very anxious, especially after midnight. They may panic and not be able to settle because they feel restless. An upset tummy before the exam often accompanies the symptoms.
Other symptoms may include: an upset tummy or diarrhoea, thirsty, cold.

Gelsemium: Unlike Arsen-alb or arg-nit which are agitated, Gelsemium patients feel paralysed by their anxiety. They feel dull, heavy, weary, their mind goes blank, they can’t think. Anxiety about performance, fear of failure. Avoid people, want to hide.
Other symptoms may include: headaches, weak muscles and shaky legs, trembling hands. ‘Flu’ symptoms, heavy, droopy eyes, painless diarrhoea. Constantly want to wee. Drowsy, but sleep is restless.

Kali Phos: supports the nervous system during prolonged excitement, overwork or worry. Headache, weakness and exhaustion in burnt-out students. Oversensitive, delicate, overwhelmed, afraid of a breakdown. Worry about their family.
Tissue salts or other low potency can be used frequently.
Other symptoms may include: buzzing in the ears. Weak eyesight.

Lycopodium: Sometimes boastful, bossy, super-confident or overbearing, but underneath, they lack confidence. They fear failure but hide it well.
Despite all the worrying they tend to do fine in the actual exam, once they get started.
They can be irritable, especially at home with the family. Very hard working and tend to over-prepare. May miss letters and words when reading or speaking.
Physically the anxiety shows in.
Worst around tea time – between 4pm and 8pm – or if they have missed a meal.
Other symptoms may include: digestive symptoms, including gurgling, bloating and wind. Headaches. Crave sweets.

Nux vomica: very competitive, high achievers, perfectionists, intolerant of others. Irritable and bad tempered, active, burn the candle at both ends, use drugs and alcohol, over eat, then get an upset tummy, heartburn, constipation or a headache.

Phosphorus: Many fears and anxieties, especially of being alone, the dark, ghosts, and thunderstorms. Fears and anxieties always relieved in company. Sensitive, sociable and friendly people, sympathetic, imaginative, startle easily.
Other symptoms may include: crave sweets, ice cold drinks, ice cream, spicy food. Sensitive to smell and sound.

Silica: timid, lack confidence, may give up and not try. Indecisive, exhausted. May over-prepare. Self conscious, anxiety in public, hate public speaking, startle easily. May also be very stubborn.
Other symptoms may include: teenagers who have grown very rapidly. Sweaty heads, smelly feet. Acne.

Bach Flower-Rescue Remedy: Use liberally for nervousness before and during exams. If you are allowed to take in a water bottle, you can add a few drops of ‘Rescue Remedy’.

 


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