Showing posts with label vaccinations. Show all posts

Friday, 20 May 2016

HPV Vaccines Toxic: Lead Developer of HPV Vaccines Comes Clean to Warn Parents & Young Girls

HPV Vaccines Toxic

Lead Developer of HPV Vaccines Comes Clean to Warn Parents & Young Girls

Gardasil, the vaccine that supposedly protects young girls from the human papillomavirus and the cervical cancer which it can lead to, has come under intense scrutiny from medical professionals around the world over the past few years. Unfortunately, mainstream media outlets rarely if ever share information related to this scrutiny, despite the many eye-opening revelations which have made their way into the public domain.

This is why I commonly write about the HPV vaccine and continue to push this information; because it’s not really openly discussed, but should be.

One of these revelations comes from Dr. Dianne Harper, one of a select few specialists in OB/GYN (in the world) who helped design and carry out the Phase II and Phase III safety and effectiveness studies to get Gardasil approved. There are only 50 HPV experts in the world, and Dr. Harper is one of them, inarguably making her an expert on the subject.

Since Harper’s involvement in getting Gardasil approved, she has condemned the vaccine, stating that it is neither safe nor effective. She has mentioned that the tested length of the efficacy of the vaccines in preventing HPV infection is not long enough to prevent cervical cancer, which, as she states, can take decades to develop. She has also stated that vaccination will not decrease the number of cervical cancer cases, but a routine of regular pap smears will.

Of all the women who get an HPV infection, approximately 70 percent of those will clear that infection all by themselves in the first year. You don’t even have to detect it or treat it. Within two years, approximately 90 percent of those women will clear it all by themselves. By three years, you will have 10 percent of that original group of women left who still have an HPV infection, and 5 percent of this 10 percent will have progressed into a pre-cancerous lesion. So, “now you have that small group of women who have pre-cancerous lesions and now let’s look at that moving into invasive carcinoma. What we know then is that amongst women with. . . [pre-cancerous] lesions. . . it takes five years for about twenty percent of them to become invasive carcinomas. That’s a pretty slow process. It takes about thirty years for forty percent of them to become invasive cervical carcinomas.” (source)

This begs the question, why do nine-year old girls need vaccinations for symptomless venereal diseases that their immune systems kill anyway?

Harper has told CBS that these vaccines are essentially useless, explaining that “the benefit to public health is nothing, there is no reduction in cervical cancers, they are just postponed, unless the protection lasts for at least 15 years, and over 70% of all sexually active females of all ages are vaccinated.”

She also goes on to caution of their dangers:

Parents and women must know that deaths occurred. Not all deaths that have been reported were represented in Dr. Slade’s work, one-third of the death reports were unavailable to the CDC, leaving the parents of the deceased teenagers in despair that the CDC is ignoring the very rare but real occurrences that need not have happened if parents were given information stating that there are real, but small risks of death surrounding the administration of Gardasil.

“It is a vaccine that’s been highly marketed, the benefits are over-hyped, and the dangers are underestimated.” – Dr. Chris Shaw, Professor at the University of British Columbia, in the department of Neuroscience, Ophthalmology, and Visual Sciences (Taken from the One More Girl documentary)

“When one looks at the independent literature, so studies which are not sponsored by the vaccine manufacturers, so with relation to Gardasil there have been several reports documenting multiple sclerosis and encephalitis, which is brain inflammation, in girls who have received their Gardasil vaccine. So just because a study sponsored by the manufacturers does not identify problems with the vaccine does not necessarily mean that the vaccine is safe. In fact if one looks at the manufacturer studies, they’re often not designed to detect serious adverse events. There was a study done by a group of researchers sponsored by Glaxo Smith and Kline and they were looking at Cervarix, which is another HPV vaccine, and the authors acknowledged that none of the studies that they evaluated have been designed to detect autoimmune diseases. So obviously, you’re not going to find what you’re not looking for. And in spite of these obvious flaws, they concluded that there is no evidence that Cervarix is associated with increased risk for autoimmune diseases, and this is absurd because you haven’t looked for it, the study has not been designed to detect autoimmune diseases.”

– Dr. Lucija Tomljenovic, PhD, Post-doctoral Fellow at the University of British Columbia, where she works in Neurosciences and the Department of Medicine (source)

Brand New Study Outlines Why Many Doctors Don’t Recommend HPV Shots

A brand new study recently published in the journal Pediatrics has found that many paediatricians don’t strongly recommend the HPV vaccine. For those of you who are unaware, the HPV vaccine, also known as the Gardasil vaccine, is designed to protect against four types of human papillomavirus, or HPV. Although the HPV vaccine is banned in multiple countries, like Japan for example, it has been approved for use in Canada and approximately 100 other countries.

Researchers used a national survey asking approximately 600 doctors to outline their stance on the HPV vaccine. Conducted between October 2013 and January 2014, the study found that a large percentage of paediatricians and family doctors — nearly one third of those surveyed — are not strongly recommending the HPV vaccine to parents and preteens, which is why, as illustrated by the study, HPV vaccination rates continue to drop.

The study mentioned that some doctors felt the need for a clearer understanding of reasons to vaccinate preteens, particularly given the fact that most do not become sexually active until later on in life, and that many parents would object to them assuming otherwise.

Prior to this, another study was published in the journal Cancer Epidemiolog in 2015. Written by Melissa B. Gilkey, an assistant professor at Harvard Medical School, the study was designed to assess how physicians recommend the HPV vaccine. The authors were surprised to find that “physicians so often reported recommending HPV vaccination inconsistently, behind schedule, or without urgency. Of the five communication practices we assessed, about half of physicians reported two or more practices that likely discourage timely HPV vaccination.” (source)

This study found that 27 percent of physicians across the United States do not strongly endorse HPV vaccination, and 39 percent reported that they do not give the vaccinations on time as recommended. Approximately 59 percent of physicians recommended it for adolescents.

Physicians questioning vaccine safety seems to be a growing trend, and this is evident and expressed in multiple publications. For example, a fairly recent study published in the journal Human Vaccines & Immunotherapeutics emphasized that “more research is needed to understand why some health professionals, trained in medical sciences, still have doubts regarding the safety and effectiveness of vaccination.” (source)

A new study published in the journal EbioMedicine outlines how more and more physicians, more specifically those in France, do not follow the recommended vaccination schedule and have hesitancy with regards to vaccination for a number of reasons, mainly due to a lack of trust in pharmaceutical grade products, their perception of the utility and risks of vaccines, and their comfort in explaining them to patients. (source)

American College of Pediatricians Links HPV Vaccine (Gardasil) To “Very Rare But Serious Condition.”

“It has recently come to the attention of the College that one of the recommended vaccines could possibly be associated with the very rare but serious condition of premature ovarian failure (POF), also known as premature menopause. There have been two case report series (3 cases each) published since 2013 in which post-menarcheal adolescent girls developed laboratory documented POF within weeks to several years of receiving Gardasil, a four-strain human papillomavirus vaccine (HPV4).”

The press release goes on to state that adverse reactions are not commonly caused by the vaccine, and that there has not been a noticeable rise in POF cases in the last 9 years that the vaccine has been widely used. This is not the first time a statement from a government medical agency has contradicted the evidence of various scientists and doctors around the world. Nevertheless, it’s great to see them at least acknowledge these potentials, stating that there are “legitimate concerns that should be addressed.” These concerns, according to them, are as follows:

Long term ovarian function was not assessed in either the original rat safety studies, or in the human vaccine trial
Most primary care physicians are probably unaware of a possible association between HPV4 and POF and may not consider reporting POF cases or prolonged missing menstrual periods to the Vaccine Adverse Event Reporting System (VAERS)
Potential mechanisms of action have been postulated based on autoimmune associations with the aluminum adjuvant used and previously documented ovarian toxicity in rats from another component, polysorbate 80
Since licensure of Gardasil in 2006, there have been about 213 VAERS reports involving amenorrhea, POF or premature menopause, 88 percent of which have been associated with Gardasil

“The overwhelming majority (76%) of VAERS reports since 2006 with ovarian failure, premature menopause, and/or amenorrhea are associated solely with Gardasil. . . . A Vaccine Safety Datalink POF study is planned to address an association between these vaccines and POF, but it may be years before results will be determined. Plus, POF within a few years of vaccination could be the tip of the iceberg since ovarian dysfunction manifested by months of amenorrhea may later progress to POF.”

It’s also worth mentioning that more than a dozen girls recently came forward in Europe claiming that they are suffering from acute physical side effects from the HPV vaccine. You can read more about that here.

Concordia Professor Criticizes HPV Vaccine After Winning A Federal Grant To Study It

Dr. Genevieve Rail, Professor of Critical Studies of Health at Concordia University, recently received a grant of $270,000 from the Canadian Institute for Health Research (CIHR) to study the Human Papillomavirus (HPV). She concluded that there is absolutely no proof that the human papillomavirus directly causes cervical cancer.

“I’m sort of raising a red flag, out of respect for what I’ve found in my own study, and for the despair of parents who had totally perfect 12-year-olds who are now in their beds, too tired to go to school,” she said. “Yes, we’re going against the grain, and we are going against those who are believed, i.e. doctors and nurses and people in public health.” (source)

She feels there are “serious concerns” about the vaccine, yet no research on how young people “experience” the vaccine. (source)

You can read more about this story here.

Merck’s Former Doctor Predicts Gardasil To Become The Greatest Medical Scandal of All Time

Dr. Bernard Dalbergue is a former pharmaceutical industry physician with Gardasil manufacturer Merck who has started to raise his voice against the HPV vaccine, and against the pharmaceutical industry as a whole. He joins a long list of experts from within the industry who have slammed the rampant manipulation and control of clinical research done by the pharmaceutical industry.

This quote is taken from an interview that happened in April of 2014, from an issue of the French magazine Principes de Santé (Health Principles):

The full extent of the Gardasil scandal needs to be assessed: everyone knew when this vaccine was released on the American market that it would prove to be worthless. Diane Harper, a major opinion leader in the United States, was one of the first to blow the whistle, pointing out the fraud and scam of it all.I predict that Gardasil will become the greatest medical scandal of all time because at some point in time, the evidence will add up to prove that this vaccine, technical and scientific feat that it may be, has absolutely no effect on cervical cancer and that all the very many adverse effects which destroy lives and even kill, serve no other purpose than to generate profit for the manufacturers. Gardasil is useless and costs a fortune! In addition, decision-makers at all levels are aware of it! Cases of Guillain-Barré syndrome, paralysis of the lower limbs, vaccine-induced MS and vaccine-induced encephalitis can be found, whatever the vaccine. (source)

Dr. Dalbergue has also recently released a book titled Omerta dans les labos pharmaceutiques: Confessions d’un medicine which goes into more detail about corruption in the medical/pharmaceutical industry. He also recently made an appearance on a popular radio show in France which you can watch here. Althought it’s in French, it’s nice to put a face to the name so that you can see he is real.

Gardasil Contains More Than Double The Amount Of Aluminum Than It Previously Had

Gardasil, like several other vaccines, contains aluminum. Health authorities will tell you that using aluminum as an adjuvant in vaccines is completely safe, but what they won’t tell you is that there are no safety assessments (toxicity studies) for vaccine ingredients. This can be quite eye-opening for those who were not already aware of this, especially considering the fact that aluminum has been being added to vaccines for approximately 90 years. Yet the Food and Drug Administration, or any other government agency for that matter, has not conducted or included appropriate toxicity studies/testing proving the safety of aluminum. Why is this? One reason could be that vaccines have traditionally (over the years) been viewed as non-toxic substances, therefore not warranting such research. (source)

“I have a document from 2002 from the US Food and Drug Administration (FDA)… discussing the assessment of vaccine ingredients… and testing specifically in animal models. Back then, the FDA stated that the routine toxicity studies in animals with vaccine ingredients have not been conducted because it was assumed that these ingredients are safe. When I read that I was kind of pulling my hairs out [thinking] ‘So, this is your indisputable evidence of safety?’ These documents never made it to mainstream media. It’s just a lie perpetuated over and over again; that we’ve been using these things for over nine decades and it’s been proven safe. No, it’s been assumed safe.”

– Dr. Lucija Tomljenovic (source)

Even if we look at the FDA’s current website/guidelines, this is not a secret. The statement above was made in response to their 2002 guidelines, which is a fairly recent document. More than 10 years later, however, despite all of the studies demonstrating clear cause for concern, not much has changed.

“Until recently, few licensed vaccines have been tested for developmental toxicity in animals prior to their use in humans.” (source)

Studies also continue to emerge every single year stressing the need to actually test vaccine ingredients for safety. You’d think this would be a no-brainer, wouldn’t you?

Here is a study published in 2015 that stresses how important it is for us to further examine the inclusion of mercury and aluminum in vaccines, arguing that “the safety levels of these substances have never been determined, either for animals or for adult humans—much less for fetuses, newborns, infants, and children.” (source)

A growing number of studies have linked the use of aluminum adjuvants to serious autoimmune outcomes in humans. (source)(source)(source)(source)

Below is an excerpt from a paper that was published in 2015 in the journal Frontiers In Neurology which emphasizes various concerns about aluminum in vaccines:

The conceptual link between long-term persistence of alum particles within macrophages at the site of previous immunization, and the occurrence of adverse systemic events, in particular neurological ones, has long remained an unsolved question. Aluminum has long been identified as a neurotoxic metal, affecting memory, cognition and psychomotor control, altering neurotransmission and synaptic activity, damaging the blood–brain barrier (BBB), exerting pro-oxidant effects, activating microglia and neuroinflammation, depressing the cerebral glucose metabolism and mitochondrial functions, interfering with transcriptional activity, and promoting beta-amyloid and neurofilament aggregation (56). In addition, alum particles impact the immune system through their adjuvant effect and by many other means. They adsorb vaccine antigens on their surface, which protect them from proteolysis thus forming a persistently immunogenic pseudo-pathogen (57). Alum particles may also bind undesirable residual products inherent to vaccine production procedures, as shown for HPV DNA sequences (58) or yeast proteins (59) that may be potentially hazardous (60). Finally, alum particles can directly induce allergy (61, 62) as other metals (63) Concerns about long-term biopersistence of alum largely depend on the ability of alum particles to reach and exert toxicity in remote organs. This ability has been suggested by several studies.

Here is another paper, published in 2013 in the journal Immunome Research, which provides further evidence of the dangers associated with aluminum in vaccines.

A study published in the journal Current Medical Chemistry in 2011 does the same:

Aluminum is an experimentally demonstrated neurotoxin and the most commonly used vaccine adjuvant. Despite almost 90 years of widespread use of aluminum adjuvants, medical science’s understanding about their mechanisms of action is still remarkably poor. There is also a concerning scarcity of data on toxicology and pharmacokinetics of these compounds. In spite of this, the notion that aluminum in vaccines is safe appears to be widely accepted. Experimental research, however, clearly shows that aluminum adjuvants have a potential to induce serious immunological disorders in humans. In particular, aluminum in adjuvant form carries a risk for autoimmunity, long-term brain inflammation and associated neurological complications and may thus have profound and widespread adverse health consequences.

Another one published in the Journal of Inorganic Biochemistry shared the following conclusions:

We show that Al-adjuvanted vaccines may be a significant etiological factor in the rising prevalence of ASD. We also show that children from countries with the highest ASD prevalence appear to have a much higher exposure to Al from vaccines, particularly at 2 months of age. . . . According to the FDA, vaccines represent a special category of drugs as they are generally given to healthy individuals [15]. Further according to the FDA, ‘this places significant emphasis on their [vaccine] safety’ [15]. While the FDA does set an upper limit for Al in vaccines at no more than 850 μg/dose [89], it is important to note that this amount was selected empirically from data showing that Al in such amounts enhanced the antigenicity of the vaccine, rather than from existing safety data or from the basis of toxicological considerations [89]. . . . Nonetheless, given that the scientific evidence appears to indicate that vaccine safety is not as firmly established as often believed, it would seem ill advised to exclude pediatric vaccinations as a possible cause of adverse long-term neurodevelopmental outcomes, including those associated with autism.

The list regarding the concerns about aluminum goes on and on. Below is a video from Dr. Christopher Shaw, a professor at the University of British Columbia in the department of Neuroscience, Ophthalmology, and Visual Sciences.

Again, a growing number of studies have clearly demonstrated aluminum adjuvants in vaccines could be a factor in the development of serious autoimmune outcomes in humans. (source)(source)(source)(source)

Moreover, we know, from the work of Richard Flarend, that aluminum is commonly absorbed into the body — into areas it shouldn’t be — and has been found in various urine samples from multiple studies examining this topic… and that’s not just for aluminum in vaccines.

“We increasingly have this compound that was not part of any biochemical process on Earth, that can now only go and do havoc, which is exactly what it does. It causes all kinds of unusual biochemical reactions.” – Dr. Chris Shaw, a neuroscientist and professor at the University of British Columbia

Here is a great video by Dr. Christopher Exley, Professor of Bioinorganic Chemistry at Keele University and Honorary Professor at UHI Millennium Institute. He is known as one of the world’s leading experts on aluminum toxicity.

From Collective Evolution @ http://www.collective-evolution.com/2016/04/12/lead-developer-of-hpv-vaccines-comes-clean-to-warn-parents-young-girls/

For more information about toxic vaccines see http://nexusilluminati.blogspot.com/search/label/vaccination

For more information about Gardasil see http://nexusilluminati.blogspot.com/search/label/gardasil
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Tuesday, 4 August 2015

Herd Immunity: Flawed Science and Mass Vaccination Failures

By Suzanne Humphries, MD

The oft-parroted sound bite – "we need herd immunity"- implies that if ninety five percent of the population can become "immune" to a disease via vaccination, target immunity levels will be met and diseases will either be eradicated or controlled. This sound bite is the most commonly pulled weapon used by the vaccinators, only second to "smallpox and polio were eradicated by vaccination." "Herd immunity" is the trump card for the defense of vaccination on TV, Internet, medical journals and newspapers as to why we should be vaccinated over and over throughout our lives, with an ever-increasing number of vaccines.

Paul Offit smiled and PLAYED THE CARD while peddling his book on the comedy central channel as Steven Colbert jokingly said, "if the vaccines work so good for you, why do I need one?" Dr. Mark Segal PULLED IT on fox news as Mary Holland, JD eloquently described the issue of vaccine injury and loss of legal recourse in an era of forced and mandated vaccines. In addition to flaunting several false allegations and sound bites, Dr. Segal's well-rehearsed rant brushed right over the issue at hand, the fact that victims of vaccine injury have no legal right to sue – and instead launched into his agenda of scaring the listeners by parroting the "herd immunity" dogma.

The hype about herd immunity unfortunately creates a wall of hostility between those who vaccinate and those who delay some vaccines, avoid certain vaccines, or quit vaccinating altogether.

Since the beginning of vaccination, there is little proof that vaccines are responsible for eradicating disease even when herd immunity vaccination levels have been reached. Yet celebrity doctors rattle on about your unvaccinated neighbor being the biggest threat to your child – as if vaccination was the only way to avoid an illness or stay healthy.

To make matters worse, this intimidation to vaccinate is played out in an environment where WHO and vaccine manufacturers have been accused of scandalous misrepresentations of disease risk or vaccine safety and effectiveness. If the allegations against these entities are true, which I believe they are, we are being systematically altered, sickened and manipulated by powerful governing bodies that either don't understand the risks of vaccination, or don't care. We are told that the health of the herd is more important than any single life, and you now have no conventional legal recourse when your little sheep is wounded by any type of vaccine, no matter how it happened.

The Money Factor

The population of the world is expanding over the past 200 years where vaccines have been used, and this makes obtaining herd immunity even more expensive and impossible today than ever. How many billions of people would need to be vaccinated how many times to eradicate just one illness based on the theory of vaccine herd immunity? How much would that cost? Consider the cost of vaccines, refrigeration, vaccinators, and hazardous waste removal. Just look at chicken pox vaccine at $7.25 per dose for the CDC discounted price. Each child gets 2 doses.

The US census shows 25.7 million children between 0-5 years. Just the cost of the vaccines to vaccinate each of those children, not including the lifetime of boosters, refrigeration, administration and waste, costs the government over 372 million dollars. Chicken pox vaccines are now being exposed for the failure they are, but vaccine profits are still climbing. After the members of the herd stopped transmitting natural immunity to each other because of the vaccine effect, shingles increased. The response- more doses of vaccine for children and a shingles vaccine to adults. There is a recent journal abstract describing the failure of herd protection by varicella vaccines. In a SEPARATE DOCUMENT, Dr. Goldman says:

"Prior to the universal varicella vaccination program, 95% of adults experienced natural chickenpox (usually as school aged children)—these cases were usually benign and resulted in long term immunity. This high percentage of individuals having long term immunity has been compromised by mass vaccination of children which provides at best 70 to 90% immunity that is temporary and of unknown duration—shifting chickenpox to a more vulnerable adult population where chickenpox carries 20 times more risk of death and 15 times more risk of hospitalization compared to children.

Add to this the adverse effects of both the chickenpox and shingles vaccines as well as the potential for increased risk of shingles for an estimated 30 to 50 years among adults. The Universal Varicella (Chickenpox) Vaccination Program now requires booster vaccines; however, these are less effective than the natural immunity that existed in communities prior to licensure of the varicella vaccine."

In India, doctors are concerned about profit margins being protected before human lives, with recommendations to vaccinate every child with more expensive, newer vaccines. Dr Jacob Puliyel describes the problems he sees..

"An analysis in the Lancet showed how the Pneumococcal vaccine reduces only 4 cases of pneumonia per 1000 children. The cost for vaccinating 1000 children comes to $ 12,750. Treating the 4 cases of pneumonia in India using WHO protocol, would cost $ 1. The pneumococcus strains prevalent in India are nearly all sensitive to inexpensive antibiotics like penicillin. In the US which has been using the pneumococcal vaccine for some years now, there has been a strain shift – strains covered in the vaccine are being replaced by other strains. Ominously the new strains are more antibiotic resistant. Vaccine has simply made the problem of pneumococcal disease worse. Yet this vaccine is being pushed in Africa and Asia....It is not about lives lost in poor countries – it is all about the cash register. These organizations and their sponsors have profit margins to protect. Ethics is not a major issue with them."

The profits to vaccine manufacturers and the government must be enormous.

The CDC is in the vaccine business. Members of the CDC's Vaccine Advisory Committee accept payment from vaccine manufacturers. Sanofi-Pasteur, Merck and others specifically seek to employ CDC staff once their contracts have run out. Relationships have included sharing a vaccine patent, owning stock in a vaccine company, payments for research, payment to monitor manufacturer vaccine tests, and funding academic departments. Thanks to a 1980 law, the CDC currently holds dozens of licensing agreements. It also has numerous ongoing projects to collaborate on new vaccines.

The science?

What science is there behind the belief that the herd can be protected by vaccinating enough of the sheep? Or that any disease has been eradicated from the planet thanks to a vaccine?

Recently, I was told by a vaccinator that "herd immunity is just a definition and so it can't actually be wrong. " But the assumption of a 95% vaccination rate giving the herd a chance at eradication or higher levels of health – can be wrong. Let us go back in time and see just where the idea behind this definition probably comes from. Dr A.W. Hedrich in 1929, studied the natural occurrence of measles.

"On the basis of field surveys of various workers, it is inferred that approximately 95% of the children in cities suffer measles attacks by the fifteenth birthday. " [1]

Before vaccines, outbreaks of measles were observed in 2 to 3 year cycles, and 95% of the population developed immunity by the age of fifteen.

The original idea that vaccination could strengthen the herd's immunity, assumed that there was only one clinical event, and that one natural exposure equated life-long immunity. But this was not the case back when the diseases circulated freely. Vaccinators miss the point that the body defends most efficiently as a result of ongoing re-exposure.

They try to mimic this with boosters. But the vaccination plan leaves the elderly(due to vaccine-induced immunity being short-lived and antigens taken out of circulation) and the very young(due to lack of transferrable maternal immunity) more vulnerable to several diseases that were not a threat to them before vaccination. In the case of chicken pox, vaccination renders the elderly more apt to shingles infections, because the herd has now lost the continued and benign re-exposures to children with chicken pox.

Instead of figuring out why a very small number develop dangerous invasive conditions, vaccine enthusiasts recommend vaccinating as often as possible in order to protect against something that would never be a danger to the vast majority of those vaccinated. If you constantly swab throats of healthy people most would be carrying and circulating supposed pathogens, as commensals.[2] At any one time in any society, neisseriae(the bacteria isolated in some cases of meningitis) are being circulated, yet most of the time, nothing happens, other than the body notes it, defends against it, and the host has no idea that they even carried it.[3] But now that vaccines for as many types as possible have been developed, the vaccine is the answer to the problem. This is typical for diseases today.

Measles

It is well documented that prior to vaccination, cycles of natural infection added to the herd's immunity.

"The formal demonstration that both maternal antibodies and early exposure to infection are required for long-term protection illustrated that constant re-infection cycles have an essential role in building a stable herd immunity.

In a population that is not constantly exposed to the infection during early infancy under the immunologic umbrella of maternal antibodies or vaccinated thoroughly a serious risk of re-emerging infections may arise. " [4]

Vaccination creates a "quasi-sterile" environment that opens up the possibility of disease outbreaks.

"Attempts to eradicate measles virus or poliovirus eliminates antigen exposure of infants to these pathogens. Such quasi-sterile epidemiological situations may actually increase the risk of outbreaks." [5]

We know this is possible because there have been eruptions of measles in the USA in populations that were 100 percent vaccinated.

"The affected high school had 276 students and was in the same building as a junior high school with 135 students. A review of health records in the high school showed that all 411 students had documentation of measles vaccination on or after the first birthday, in accordance with Illinois law." [6]

Within the scope of vaccination, when a quasi-sterile situation is created, and measles breaks out in the midst, the only solution within that paradigm is to vaccinate more people, more often. This is a backwards solution to the problem when considering who remains susceptible even in the face of full compliance: infants and non-immune adults. Susceptible age groups have essentially traded places since vaccinating.

What used to happen with measles is that infants were protected by maternal antibodies, adults were protected by continued exposure, and infected children handled the disease normally and became immune for long periods of time. So, while measles vaccines have decreased the expression of measles infections, it has not necessarily improved the bigger picture. And certainly there are numerous troubles with the side effects of the vaccine.

Prior to vaccination, mothers were naturally immune to measles and passed that immunity to their infants via placenta and breast milk. Vaccinated mothers may have vaccine immunity, which is not the same immunologically, as natural immunity. One of the major differences in the vaccine-induced immunity is that it cannot be passed from mother to infant.

Since most vaccines are delivered by injection, the mucous membranes are bypassed and thus blood antibodies are produced but not mucosal antibodies. Mucosal exposure is what contributes to the production of antibodies in the mammary gland. A child's exposure to the virus while being breastfed by a naturally immune mother would lead to an asymptomatic infection that results in long-term immunity to that virus. Vaccinated mothers have lower levels of virus-specific antibodies in the serum and milk compared to naturally immune mothers and thus their infants are unprotected.

"Infants whose mothers were born after 1963 had a measles attack rate of 33%, compared to 12% for infants of older mothers." Infants whose mothers were born after 1963 are more susceptible to measles than are infants of older mothers. An increasing proportion of infants born in the United States may be susceptible to measles." [7]

For the disease of measles, we see that while the clinical case rate may have declined with vaccination, the most sensitive members of the herd are at an increased risk- as a result of vaccination.

Dr Peter Aaby has produced volumes of research on measles in Africa. Initially there was a belief that measles infection was associated with immune suppression and higher long-term mortality, but that belief came from vaccine research, not natural measles research.

"The belief in persistent immune suppression was stimulated by increased mortality after high-titre measles vaccination." [8]

https://coto2.files.wordpress.com/2010/08/dees_vaccine8_med.jpg

Once natural measles was monitored long-term the knowledge changed. According to Aaby,

"When measles infection is mild, clinical measles has no long-term excess mortality and may be associated with better overall survival than no clinical measles infection. Sub-clinical measles is common among immunised children and is not associated with excess mortality." [9]

Measles is mildest when the infected person is replete with vitamins C and A. The devastation and mortality you hear about with measles comes from starving populations.

Do you know that 30% of cases of measles in unvaccinated are missed because they are so mild?[10] Subclinical measles is an entity that most doctors today are unaware of. If they are missed in unvaccinated, and there are known outbreaks of measles in 100 percent vaccinated populations, are cases missed in vaccinated populations too? Is measles still alive and well but going unnoticed in vaccinated countries, until a well-publicized outbreak occurs, as vaccine necessity is being trumpeted? What doctor would know or is even looking for atypical measles?

Talk to your grandmother about measles. Ask her if she saw death and destruction from the disease. It was not a disease that needed eradication. The high death rates were in countries where children were undernourished and lacked vitamins necessary to process the virus. Alexander Langmuir, MD is known today as "the father of infectious disease epidemiology." In 1949 he created the epidemiology section of what is now known as the CDC. He also headed the Polio Surveillance Unit that was started in 1955 after the polio vaccine misadventures. Dr Langmuir knew that measles was not a disease that needed eradication when he said:

"To those who ask me, 'Why do you wish to eradicate measles?,' I reply with the same answer that Hillary used when asked why he wished to climb Mt. Everest. He said, 'Because it is there.' To this may be added, ". . and it can be done." [11]

Langmuir also knew that by the time vaccination was developed, measles mortality in the USA had already declined to minimal levels when he described measles as a

"... self-limiting infection of short duration, moderate severity, and low fatality..." [12]

The vaccine was created because it could be done, not because we needed it. Measles is not eradicated. Outbreaks happen all over the world, and will continue. And now infants will be unprotected because of the absence of maternal antibodies in their vaccinated mother's milk. So much for protecting the most vulnerable in the herd.

Smallpox

"We were fortunate enough to address their own medical (and) health officials where we reminded them of the incidence of smallpox in formerly "immunized" Filipinos. We invited them to consult their own medical records and asked them to correct us if our own facts and figures disagreed. No such correction has been forthcoming, and we can only conclude that between 1918-1919 there were 112,549 cases of smallpox notified, with 60,855 deaths. Systematic (mass) vaccination started in 1905, and since its introduction case mortality increased alarmingly. Their own records comment that "The mortality is hardly explainable."—Dr. Archie Kalokerinos from Second Thoughts on Disease

Orthopox is a member of the family of Poxviridae. The ancestor of the poxviruses is not known but structural studies suggest it may have been an adenovirus or a species related to both the poxviruses and the adenoviruses. Orthopox viruses include cowpox(vaccinia), smallpox(variola), and monkeypox. Mutations do occur in these viruses, but at a very slow rate.

Between October 1970 and May 1971 a poxvirus was isolated from some symptomatic patients in West Africa. That virus is now known as "human monkeypox." Monkeypox got its name because monkeys were the first animals known to have harbored the monkeypox virus. Scientists now say that the primary reservoirs for monkeypox virus are not monkeys but probably squirrels. WHO officials in 1976 had no idea what the true reservoir of infection was.[13] Today, according to CDC, it remains uncertain.

Smallpox was declared eradicated worldwide by the World Health Assembly on May 8,th 1980. Vaccination was stopped in the USA in 1972. However, poxviruses that were indistinguishable from smallpox continued to cause human disease.

Monkeys in surrounding areas where monkeypox outbreaks occur usually test negative for monkeypox. But prairie dogs, exotic rodents, Gambian rats, dormice, rope squirrels and other animals have tested positive. Nobody really knows when or where monkeypox viruses originated, but they seem to be close relatives of cowpox and smallpox. All three viruses have rodent reservoirs, which is important when considering the history and current transmission of smallpox and monkeypox. Today, monkeypox outbreaks are blamed on rodents or exotic pet imports, not person-to -person transmission even though human transmission does occur. Historically, smallpox reservoirs were also rodents – during a time when rodents were eaten as food and when infestations were commonplace. Yet in the discussion of smallpox outbreaks this is rarely mentioned. What we hear is how the vaccine eradicated the disease.

THIS ARTICLE states that monkeypox was first recorded in 1970 after the eradication of smallpox in the Democratic Republic of Congo. University of California, School of Public Health epidemiologist Dr Anne Rimoin states that monkeypox first arrived in humans after smallpox eradication, even though it has been on the earth for millennia.

"Monkeypox has probably occurred for millennia in central Africa, but it's only since the eradication of smallpox that it's been a disease that actually happens in humans," Rimoin says. "

There is absolutely zero certainty as to when monkeypox first colonized humans. It is more accurate to say that monkeypox was first detected in humans around the time that smallpox was being declared eradicated, not that it arrived in humans at that time. Differentiation tests were not carried out on most cases of pox in the past 200 years.

Laboratory diagnostic assays for monkeypox include virus isolation and electron microscopy, ELISA, immunofluorescent antibody assay, histopathologic analysis, and Polymerase Chain Reaction (PCR). Unfortunately, most of these methods are relatively nonspecific and are unable to differentiate monkeypox viral infection from infection with other poxviruses.[14] All but PCR are fraught with false positives, false negatives, and cross reactivity.

In the 1970s and 1980s, biochemical tests were unreliable in differentiating between monkeypox and smallpox. Animal challenge tests were historically used to determine the difference between monkeypox and smallpox. The technique involved inoculating rabbits and watching the characteristics of the pox. Initially the two kinds of pox appear similar in the rabbit, but after a few days, monkeypox distinguishes itself as it becomes hemorrhagic. LINK TO DOC HERE.

The problem with such means for distinction is that there has always been a hemorrhagic form of smallpox.

"There are four types of variola major smallpox: ordinary; modified; flat; and hemorrhagic.... Hemorrhagic smallpox has a much shorter incubation period and is likely not to be initially recognized as smallpox when presenting to medical care. Smallpox vaccination also does not provide much protection, if any, against hemorrhagic smallpox." [15]

ELISA is not much of a gold standard test as it casts a very wide net, and is fraught with false positive and false negative results.[16] ELISA TUTORIAL HERE.

The genomes of these three orthopox viruses are extremely conserved and require a technology that can detect the minute differences. Polymerase Chain Reaction (PCR) is a newer test that came on the scene in the 1980s. This test is different in that it can potentially find pieces of DNA from a virus. The genetic sequence of a virus has to first be mapped prior to designing a PCR test. So before smallpox, cowpox, or monkeypox viruses were characterized genetically, PCR could not be applied to distinguish between them.

The first PCR test for monkeypox was used in 1997, but highly sensitive real-time PCR was not in use until 2006.[17] Different biotech companies have developed different tests that use different primers. PCR, while highly sensitive and specific at about 98%, still has drawbacks, contamination being the biggest one. No test is foolproof. Nonetheless it is probably the best assay available for detection and distinction today.

It should now be obvious that during the two centuries of smallpox vaccination and up until the 1990s there was no certain way of testing for distinct orthopox viruses. During the two centuries of vaccination, the viruses were likely to mutate, and certain strains could have been selected out as a result of vaccination.

Therefore, does anyone know how much 'smallpox' disease was actually monkeypox or vaccinia? Given that monkeypox is thought to be an ancient virus, where was it during the smallpox epidemics? Was it called hemorrhagic smallpox?

In 1972, scientists were asking similar questions when they said:

"Is it possible that there is an animal reservoir for smallpox infection? Could monkeypox be a source of new outbreaks of true variola? Or, can the monkeypox virus undergo certain mutations and become identical in its pathogenicity and infectiveness to the variola virus?" [18]

ACCORDING TO SCIENTIFIC AMERICAN, monkeypox is not that rare. Seven hundred and sixty cases of monkeypox were counted in the Congo between 2006 and 2007.

Before and during the time of eradication declaration, PCR was unavailable, and the different poxviruses couldn't be distinguished by their DNA, but by a skin test on rabbits, chick embryo membranes, and blood tests that were fraught with uncertainty. It seems to me that what was once called smallpox was likely a very non-uniform disease that could have been anything from cowpox to two forms of smallpox to chickenpox to monkeypox.

"Monkeypox virus is closely related to some other orthopoxviruses such as variola (smallpox) virus, and it cannot be distinguished from these viruses in some laboratory tests....In 1996-1997, an outbreak [of monkeypox] in the DRC continued for more than a year, with a person–to–person transmission rate estimated at 78%. However, epidemiological evidence suggests that many of the cases in this outbreak may have been chickenpox (varicella); the number of monkeypox cases and the transmission rate might have been overestimated due to self-reporting and the unavailability of laboratory testing." [19]

When vaccination stopped, monkeypox was suddenly diagnosed in humans. Diagnostic methods were absent during the great vaccine campaigns and everything pox-like was considered smallpox and counted as smallpox. Differentiating was not a priority.

Variola, the smallpox virus, is not in the smallpox vaccine. Instead, a cultured form of cowpox, called vaccinia, is the virus used to prevent smallpox. That same vaccine also covers monkeypox, according to the CDC:

Smallpox vaccine is effective at protecting people against monkeypox when it is given before they are exposed to monkeypox. (Exposure includes very close contact with a person or animal that has monkeypox.) Experts believe that vaccination after exposure to monkeypox may help prevent the disease or make it less severe." [20]

"Because the monkeypox virus is related to the virus that causes smallpox, the smallpox vaccine can protect people from getting monkeypox as well as smallpox.

Even though PCR can distinguish between the three viruses, clinically and immunologically the viruses are so similar, that one virus in the vaccine is thought to immunize against the two other viruses. During outbreaks they all look the same.

After the world trade center collapses in New York there were concerns over potential bioterrorism. Forty thousand health care workers and first responders and 450 thousand military were vaccinated in 2003. They were all contagious for the nineteen-day post-vaccine shedding period. Some doctors were asked to receive the vaccine in order to care for those who took the vaccine and developed vaccinia, or to care for those who became infected upon contact with a recently vaccinated person.

Multi-state outbreaks of monkeypox were reported in the same year.[21] Most cases are presumed to have come from contact with prairie dogs exposed to rodents per CDC. However all cases were not exposed to animals. ACCORDING TO A 2005 REPORT, of 72 cases only 37 cases were laboratory confirmed. Eleven original cases were thrown out of the database when they met exclusion criteria. EXCLUSION CRITERIA. There is mention of human to human infection, though in some reports this is denied.

This is a very strange coincidence; vaccination and concomitant pox outbreaks in the same year. Supposedly, monkeypox is not easily transmissible between humans, but there is a report in the literature of a 5 chain human-to -human transmission, and human-to-human monkeypox transmission is well documented.[22] A NEW ENGLAND JOURNAL OF MEDICINE REPORT vaguely stated that "There was 'limited or no' spread of monkeypox virus through human contact during this outbreak."

In 2003, the year that half a million people were vaccinated in the USA – AND the only year of monkeypox outbreaks in the USA, a multistate (Illinois, Indiana, Kansas, Missouri, Ohio, and Wisconsin) outbreak, was the source of the outbreak definitely prairie dogs? CDC doesn't state how many pox cases were exposed to prairie dogs, just "the majority of them had direct or close contact." The vagueness of CDC's reports gives rise to doubts. Only 37 of 72 cases were confirmed with PCR tests, and eleven of the original total were excluded from analysis. Excluding numerous cases on frivolous grounds is one way to dampen a negative outcome after a vaccine accident.

Considering the link with vaccination is not far-fetched especially given that CDC reports say that only roughly half of cases were PCR confirmed. Vaccination has long been a relatively common means of transmitting pox outbreaks. According to Arita and Gromyko's WHO bulletin in 1982, vaccination was a major fly in the eradication ointment...

"During the last 24 months, for example, surveillance reports from Canada and the United Kingdom have included 6 and 9 cases, respectively, of vaccine complications. At least 8 cases, however, were in persons who, while not vaccinated themselves, had been infected with vaccinia virus after being in contact with persons recently vaccinated. In some countries vaccination of recruits to the armed services has continued; these recruits will occasionally transmit vaccinia infection to unvaccinated persons, and inevitably some of the complications will be fatal. In the United Kingdom and Finland, smallpox vaccination of army recruits was discontinued in 1981." [23]

Without discontinuing vaccination, it would have been impossible to stop the flow of smallpox. Doesn't that lead you to wonder how much smallpox was the result of the vaccine rather than natural smallpox? We know that in places like Leicester UK, when vaccination ceased, so did smallpox. And there are numerous accounts of smallpox disease not only being much more severe and deadly among vaccinated populations, but also more prevalent.

Isn't it interesting that smallpox vaccine defies everything we know about specificity in immunity and that one vaccine covers all sorts of pox, except chicken pox? Can you imagine, nowadays, if a vaccine researcher suggested that an illness could be prevented by using a slightly related virus? Today's vaccines contain numerous strains and types of the same organism. Polio vaccine has 3 types of poliovirus, influenza 2 strains of type A and one strain of type B. But smallpox vaccine today contains one of many possible strains of a related virus, not even the smallpox(variola) virus at all. In Jenner's time, it is anyone's guess which viruses ended up in the vaccines since the technique was so primitive and typing methods were not available. Still, these vaccinia vaccines are thought to have eradicated smallpox, and serve as the foundation for vaccine faith.

Scientists back in the 1800s and early to mid 1900s had no way to differentiate smallpox, cowpox, monkeypox or most other pox diseases in humans. Nor was there any effort to differentiate, until the disease was declared eradicated – just like when polio was eradicated. Anything that looked like polio, but not caused by a polio virus, was called acute flaccid paralysis.

Monkeypox and smallpox look identical on physical examination. Have a look at these two photos:

You probably can't tell the difference between the two diseases, and neither can most doctors. Edward Jenner and the doctors of the 1800s and 1900s were also unable to distinguish smallpox – major and minor, monkeypox, or cowpox, or even chickenpox.

"When [monkeypox]infection in human beings does occur, it can be clinically indistinguishable from smallpox, chickenpox, and other causes of a vesiculopustular rash." [23A]

It is now known that many cases of smallpox were mild. These are termed variola minor. Variola major and variola minor are indistinguishable using the sensitive PCR test,[24] and thus represent the same infectious organism.

Do you think your doctor would know a case of variola minor if he/she saw it? Or would it just be called chicken pox? Do you think your doctor would even think that it could be smallpox, given that smallpox is thought to be eradicated? There are clinical means to distinguish the difference, but few doctors think of it, and in the minor forms of smallpox it wouldn't matter anyway.

Many believe that smallpox was eradicated from the planet because of vaccination. I once believed this idea that was taught to me in medical school, and that all conventional doctors parrot as if they understood the history. With just a little research it becomes evident that even though smallpox seems to have disappeared, this was not the result of mass vaccination.

It is obvious that the vaccines of 1796-1900s were not purified or uniform, yet they serve as the foundation for successful vaccination. They were made on farms from scrapings of infected cow bellies, coarsely filtered, and mixed in glycerine. While today's vaccine product may be more meticulously manufactured, the CDC admits that the science behind even modern smallpox recommendations has been little more than a guess.

"...data on duration of protection and recommendations on periodicity of vaccinations are limited and based to a large extent on historic precedent and expert opinion used to develop previous ACIP recommendations for smallpox vaccination for laboratory workers using orthopoxviruses." [25]

And CDC has no idea what antibody titer is protective.

"The levels of antibody reported by these tests indicate only exposure, and the protective antibody titer against smallpox infection is unknown." [26]

They surmise that the vaccine provides high-level immunity for 3-5 years.

Here is a graph of smallpox vaccination deaths and smallpox disease deaths, from England spanning the years of 1906-1922.

The vaccine-associated deaths are conspicuously high, at about half the rate of smallpox deaths.

Dr. Charles T. Pearce in his 1868 essay on vaccination wrote:

"It is a remarkable fact that Jenner's[the inventor of smallpox vaccine] first child, his eldest son, on whom he experimented, died subsequently of consumption[tuberculosis]. Another of his subjects, the man Phipps, whom Jenner vaccinated, also died of consumption."

Those who were vaccinated for smallpox were noted to be more severely affected by smallpox and tuberculosis. Many were exposed to tuberculosis from tuberculous animals that were used to make vaccines. CLICK HERE TO LINK TO "SMALLPOX AND THE FIRST VACCINE" CHAPTER FROM OUR UPCOMING BOOK.

Smallpox manifested in several different forms(ordinary, modified, malignant, hemorrhagic). Genetically the minor and major forms of variola are related and indistinguishable by PCR. Individual susceptibility, rather than the virus probably made the biggest difference. Susceptibility would have certainly increased after injection of filthy vaccines that contained myriad bacteria and viruses.

What is most likely is that the appearance and disappearance of epidemics had much to do with the constitution and care of the population of the times. Scurvy was common in areas with hemorrhagic smallpox. This is no surprise to anyone who understands the full spectrum of ascorbic acid's function in the body, especially on blood vessels.

Pox epidemics declined as a result of sanitation and improved nutrition. During the era of smallpox most people were living in squalor, eating no fresh food, but rotten milk and rotten meat, drinking sewer water, living among filthy rodents, and working long hours for little pay. Pox viruses are ancient, but smallpox evolved as a deadly killer as humanity devolved to overcrowded city dwellers living with filth, squalor, and desperation.

Historical evidence points to the fact that the vaccinated were amongst the sickest in times of smallpox vaccines. Protests against the vaccinators and smallpox vaccination were massive.[27] Parents commonly chose jail rather than permit their newborn babies to be vaccinated. Entire towns and districts revolted before the disease was finally declared eradicated, and the vaccine madness ended.

Smallpox vaccination ended in the 1980s because smallpox had declined and because there was so much trouble with the old unsafe vaccine. That same trouble with the newer supposedly more safe smallpox vaccines is why smallpox vaccination ended after the 2003 first responder effort. Which makes you wonder just how much more trouble there was with the old smallpox vaccine which had a very long list of known bacterial and other "contaminants" because of its method of production. After the 2003 vaccines, reports of generalized vaccinia, autoinoculation, erythema multiforme, myopericarditis, ocular vaccinia, and postvaccinial encephalitis were reported.

Smallpox was declared eradicated before clear distinctions between different poxviruses were made using DNA analysis. Symptoms alone are what were counted for smallpox during smallpox epidemics. Vaccination was a major source of smallpox outbreaks, and only a small portion of the earth's entire herd was ever even vaccinated. Considering all of this, how can anyone believe that smallpox was eradicated with a vaccine?
_____
With every vaccine suppressible disease, the general hysteria level usually depends on the availability of a vaccine. Once a vaccine was available, the disease was suddenly made out to be more problematic. Look how dangerous chicken pox became after the vaccine was developed.
_______
Pertussis is now hot news and the unvaccinated interrupting herd immunity is raised over and over, despite the science that shows the vaccinated are by far and away the most affected by whooping cough.

"Our unvaccinated and under-vaccinated population did not appear to contribute significantly to the increased rate of clinical pertussis. Surprisingly, the highest incidence of disease was among previously vaccinated children in the eight to twelve year age group." [28]

This is the most recent, but not the first study to demonstrate 86% of cases of proven whooping cough are in the vaccinated. How can getting even 100% vaccination uptake create an immune herd with such vaccines?

Mumps vaccine was known to be ineffective after two major outbreaks in vaccinated populations in the USA. Yet the solution was to double the boosters in children with a vaccine that is now ALLEGED by two former Merck scientists, to have been known to be ineffective by Merck's executives.

Jenner's initial promise was "We have a vaccine that will protect you for life with one injection." But even he was revaccinating his patients yearly, within 5 years of making that statement. And when that doesn't pan out with whooping cough, measles, mumps and whatever, the authorities say,, "We have a highly effective vaccine if it is given on time with boosters," then "This is an excellent vaccine when 3 or 4 boosters are given, and adults are revaccinated." Or in the case of whooping cough, introducing an all-together new vaccine. There is a new nasal vaccine in the pipeline for newborns, which will be given alongside the already ineffective whooping cough vaccine series in childhood. This will no doubt be touted as a wonderful combination.

Eradication target dates are constantly moved forward, and the unvaccinated or the vaccine refusers are blamed for all outbreaks. Or in the case of Pakistan, they are branded TERRORISTS or RELIGIOUS FANATICS for not wanting their children to have 30 oral polio vaccines by age 5. I have outlined in a PREVIOUS BLOG, just what is really going on in India and how her people are being terrorized by WHO and CDC as the rate of paralysis continues to skyrocket.

I believe that when diseases disappear from sight, the disappearance is never solely by virtue of the vaccine. Yet the vaccine always gets the credit, because the blind faith in vaccines is prioritized over the scientific evidence. Evidence to the contrary of the value of vaccination is consistently snuffed out and kept away from the mainstream media, so that the herd never hears a peep of the truth. Instead, they get the "herd immunity" sound bite, which gives undeserved credit to the risk-benefit ratio of vaccination. Inside the web of half-truths and misinformation, the vaccine religion somehow justifies the public display of resentment and fear of the unvaccinated.

A special thank you to "O" from "INSIDE VACCINES" for assistance in editing this document.

BIBLIOGRAPHY

1. Hedrich AW. 1930. The corrected average attack rate of measles among city children. Am. J. Epidemiol. 11 (3): 576-600.
2. Hjuler IM. 1995. Bacterial colonization of the larynx and trachea in healthy children. Acta Paediatr. 1995 May;84(5):566-8. PMID:7633155
3.Caugant DA. 2009. Meningococcal carriage and disease—population biology and evolution. Vaccine. 2009 Jun 24;27 Suppl 2:B64-70. PMID: 19464092
4. Navarini AA et al. 2010. Long-lasting immunity by early infection of maternal-antibody-protected infants. Eur J Immunol. Jan;40(1):113-6. PMID: 19877011
5. ibid. Navarini.
6. Measles Outbreak among Vaccinated High School Students – Illinois. MMWR. June 22, 1984 / 33(24);349-51 http://www.cdc.gov/mmwr/preview/mmwrhtml/00000359.htm
7. Papania M. et al. 1999. Increased susceptibility to measles in infants in the United States. Pediatrics. Nov;1045(5):e59 pp 1-6. PMID 19545585.
8. Aaby P. et al. 2002. Low mortality after mild measles infection compared to
uninfected children in rural west Africa. Vaccine. Nov 22;21(1-2):120-6. PMID:12443670
9. ibid Aaby.
10. Kandapal SD. 2003. MEASLES ANTIBODY STATUS AMONGST NINE MONTHS FIVE YEARS UNVACCINATED CHILDREN. Indian J Prev Soc Med. Vol 34 (1) pp 8-16.
11. Langmuir A.1962 .The importance of measles as a health problem. AJPH vol 52 no 2 pp1-4.
12. Ibid Langmuir.
13. Arita and Henderson. 1976. Monkeypox and whitepox viruses in West and Central Africa. Bull World Health Organ. 1976; 53(4): 347–353. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2366520/
14. Weinstein Robert. 2005. Reemergence of Monkeypox: Prevalence, Diagnostics, and Countermeasures. Clin Infect Dis. 41 (12): 1765-1771.
15.US FDA. Vaccines, blood and biologics. Smallpox. http://www.fda.gov/BiologicsBloodVaccines/Vaccines/QuestionsaboutVaccines/ucm070429.htm
16. Human anti-mouse antibodies (HAMA) are a common cause of false positive ELIZA. A person can develop HAMA for different reasons. The clinical use of monoclonal mouse antibodies (e.g., for radioimaging, in the treatment of some cancers) often produces HAMA. HAMA may also arise because of incidental or occupational exposure to foreign proteins (e.g. veterinarians, farm workers, food preparers) or due to the presence of domestic animals in the home environment. Blood transfusion and dialysis are among other sources of heterophilic antibodies.
17. http://ci.vbi.vt.edu/pathinfo/pathogens/MPV.html
18. Is monkeypox a reservoir of smallpox? December 25, 1972. JAMA. 1972;222(13):1645-1646. http://jama.jamanetwork.com/article.aspx?articleid=346137
19. Monkeypox. 2009. Center for food security and public health. Iowa state university. Pg 1-9. www.cfsph.iastate.edu/Factsheets/pdfs/monkeypox.pdf
20. CDC Fact Sheet. Smallpox vaccine and monkeypox. http://www.cdc.gov/ncidod/monkeypox/smallpoxvaccine_mpox.htm.
21. US CDC. MMWR. July 11, 2003 / 52(27);642-646. Update: Multistate Outbreak of Monkeypox — Illinois, Indiana, Kansas, Missouri, Ohio, and Wisconsin, 2003. http://www.cdc.gov/mmwr/preview/mmwrhtml/mm5227a5.htm
22. Fenner et al. 1989. Smallpox and its eradication. Page 1306.ISBN-10: 9241561106
23. Arita and Gromyko. Surveillance of orthopoxvirus infections, and associated research, in the period after smallpox. Bull World Health Organ. 1982; 60(3): 367–375. PMCID: PMC2536002 eradication
23A. Lancet Review. Jan 2004. Monkeypox. vol 4. pp 21-25.
24. Loveless BM. 2009. Differentiation of Variola major and Variola minor variants by MGB-Eclipse probe melt curves and genotyping analysis. Mol Cell Probes. 2009 Jun-Aug;23(3-4):166-70. Epub 2009 Apr 5. http://www.ncbi.nlm.nih.gov/pubmed/19345728
25. US CDC Emergency preparedness and response. CDC Interim Guidance for Revaccination of Eligible Persons who Participated in the US Civilian Smallpox Preparedness and Response Program. http://www.bt.cdc.gov/agent/smallpox/revaxmemo.asp
26. US CDC. Emergency preparedness and response. Questions and Answers About Post-event SmallpoxVaccination http://www.bt.cdc.gov/agent/smallpox/faq/post_event.asp
27. Durbach, Nadja. 2004. Bodily Matters: The Anti-Vaccination Movement in England, 1853–1907. ISBN-10: 0822334127
28. Witt M et al. 2012. Unexpectedly Limited Durability of Immunity Following Acellular Pertussis Vaccination in Pre-Adolescents in a North American Outbreak. Clin Infect Dis. Clin Infect Dis. 2012 Jun;54(12):1730-5. PMID:22423127

Dr. Suzanne Humphries is a conventionally educated medical doctor who has taken the walk into, around, and out of the allopathic paradigm. She fully and successfully participated in the conventional system for 19 years, witnessing first-hand how that approach fails patients and creates new disease time and again. Prior to medical school, she earned a bachelor’s degree in physics from Rutgers University.

Dr. Humphries is on the board of directors of the International Medical Council on Vaccination. She lives in Maine, USA.

Visit her website is drsuzanne.net

From Green Med Info @ http://www.greenmedinfo.com/blog/herd-immunity-flawed-science-and-mass-vaccination-failures

For more information about vaccination see http://nexusilluminati.blogspot.com/search/label/vaccination

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