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Millions of children across Africa have been included in meningitis vaccine trials, many without parental consent. VacTruth recently revealed this information, resulting in many agencies desperately trying to cover up this travesty and the sacking of two leading heads of state.

Shortly after VacTruth published the first of three articles covering the MenAfriVac vaccine tragedy in which dozens of children were paralyzed, in Gouro, Chad, in northern Africa, the prime minister of Chad, Emmanuel Nadingar, was relieved of his duties and replaced by the former chief of cabinet, Djimrangar Dadnadji. According to an excellent article by the human rights organization Ecoterra International, this abrupt change in leadership was ordered by Chad’s president Idris Déby, a patron of the anti-meningitis campaign. [1]

BIG NAMES, BIG MISTAKE

On January 13, 2013, VacTruth published the second of the three articles. By this time, Chadian authorities had reported that a total of 38 children who were suffering from adverse reactions to the vaccine had been evacuated to hospitals in N’Djamena, Chad’s capital. [2]

A few weeks later, VacTruth was informed that the health minister of Chad, Mamouth Nahor N’Gawara, had also been relieved of his duties and replaced by Dr. Mahamat Ahmat Djidda. [3]

So, why the sudden changes in leadership? It may have had something to do with the fact that VacTruth had reported the conflicting views from involved organizations on whether or not the MenAfriVac vaccine could be used outside of the usual controlled temperature chain (CTC) of 2 – 8 °C.

The organizations involved with the promotion of the vaccine had stated that MenAfriVac was a vaccine specifically designed to meet the needs of Africa’s meningitis belt, which stretches across sub-Saharan Africa. These organizations stated that the vaccine could be kept in a controlled temperature chain (CTC) at temperatures of up to 40°C for up to four days without the need for ice packs or refrigeration.

The organizations involved in the promotion of this information were the CDC, FDA, BMGF, PATH, MVP, WHO and UNICEF. (For meanings of these acronyms, please refer to key at the end of this article.)

YOU WON’T BELIEVE WHAT HAPPENED NEXT

Of course this information would have been fantastic news for Africa, except for one vital point: at the time we published our articles, Serum Institute of India, the manufacturer of the vaccine, was promoting conflicting information. They had stated on their website:

“MenAfriVac should be stored and transported between 2-8ºC. Protect from light. The diluent should be stored at 25°C. It is recommended to protect the reconstituted vaccine from direct sunlight. Do not exceed the expiry date stated on the external packaging.

Here is a snapshot of the original page.

An archived snapshot of the vaccine manufacturer’s website show they changed information about the storage of the vaccine shortly after the children became paralyzed.

However, when this information was checked for verification last week, the recommendations for vaccine storage had mysteriously changed to the following statements:

“MenAfriVac should be stored and transported between 2-8ºC. Protect from light. The diluent should be stored at 25°C. It is recommended to protect the reconstituted vaccine from direct sunlight. Do not exceed the expiry date stated on the external packaging. Immediately prior to reconstitution the vaccine is stable and can be used when exposed up to 40ºC for period of 4 days provided the vaccine has not reached its expiry date and the vaccine vial monitor has not reached the discard point.” [4]

Why was this information suddenly changed, after the vaccine had already been stored and administered according to the previous guidelines? Was it because we reported that dozens of children were paralyzed and suffering other adverse reactions after receiving MenAfriVac? Was it because we reported that this vaccine was administered to third-world children before it was licensed?

In October 2012, WHO had stated:

“The session began with an introduction by Mr. Michel Zaffran, who highlighted the groundbreaking progress made with MenAfriVac®, which will be the first EPI vaccine licensed for use in a controlled temperature chain (CTC).

… This is the final review of the document by IPAC prior to the planned field testing during the MenAfriVac® campaign in Benin in November 2012, where one district will use the vaccine in a CTC. After the field testing has been conducted, the revised final guidance document will come back to IPAC for endorsement in 2013.”[5]

The reasons why the manufacturer suddenly changed their recommendations for storage and transport remain a mystery. However, this new controversy still does not take away the fact that MenAfriVac was not licensed to travel in a CTC of temperatures of up to 40°C at the time the children of Gouro were vaccinated.

THIS DOESN’T MAKE SENSE!

What exactly is a controlled temperature chain? If these vaccines do not need refrigeration or ice packs for up to four days, how does the word “controlled” come into the process? Surely, without ice packs or refrigeration, there is no controlled temperature chain.

MenAfriVac is an inactivated vaccine (a vaccine which does not use a live virus). Previously, according to the CDC guidelines for vaccine temperature and storage, inactivated vaccines needed refrigerator storage at temperatures between 35°F and 46°F (2°C to 8°C), with a desired average temperature of 40°F (5°C). (Note, that is 40°F not 40°C.) [6]

So, what makes the MenAfriVac vaccine so different from other vaccines, that it does not require refrigeration for up to four days?

Another important point to consider is the fact that temperatures across Africa can exceed 40°C. According to the website Weather Spark, the average weather for N’Djamena, Chad varies between 15°C and 41°C. Their temperatures are rarely below 12°C or above 44°C. This means that outdoor temperatures can reach 44°C in a typical year. [7] In fact, in June 2010, temperatures in Chad reached an all-time high of 47.6°C. [8]

MORE UNANSWERED QUESTIONS

This information leads me to ask the following questions:

If the outdoor temperatures can reach 44°C in a typical year and the MenAfriVac vaccine is traveling inside a vehicle which may not have air-conditioning, in a container without ice packs or refrigeration, then how do the vaccinators know the true temperature the vaccine has reached at any given time?

If the truck carrying the vaccines is traveling across Africa at the time that the outdoor temperatures rise above 40°C, does the team return to base and scrap that particular batch of vaccines?

Can both the vaccine and the diluents be kept at the same temperature?

I ask the third question because it is usual for the vaccine and the diluents to be kept at different temperatures in accordance with recommendations from the manufacturer and the CDC.

ANOTHER SUSPICIOUS TRIAL

Another interesting point to consider is this: at the time the MenAfriVac vaccine was being administered to the children in Gouro, it was being tested to see whether or not it was safe to be administered to children in temperatures of up to 40°C. Therefore, it is odd that the vaccinators chose to vaccinate the children at the time of year when temperatures are usually below 30°C.

The children of Gouro were not the only children being used in clinical trials for the MenAfriVac vaccine. Babies between the ages of 14 –18 weeks were also being used for clinical trials in Ghana.

According to the Meningitis Vaccine Project (MVP), a MenAfriVac phase 2 clinical trial was carried out in Ghana, testing the vaccine for use in the under-one age group. The trial was carried out over a four-year period from November 2008 to November 2012 at the Navrongo Health Research Center, Navrongo, Ghana. A total of 1,200 infants took part in the trial, aged between 14 to 18 weeks on enrollment. MVP stated:

“Study results: Preliminary results show that the vaccine is safe and highly immunogenic. Final results will be presented in a forthcoming scientific publication.” [9]

The MVP News Digest reported the following:

“Research to document an indication for MenAfriVac™ use in infancy (in under 1-year-olds) is progressing well and according to schedule. A database lock for PsA-TT-004 was completed on December 21. PsA-TT-004 is a Phase 2 study that evaluates the safety and immunogenicity of different dosages and schedules of the MenA conjugate vaccine in 1,200 healthy infants when administered concomitantly with EPI vaccines. The study is conducted at the Navrongo Health Research Centre in Ghana and is scheduled for completion in early 2013.” [10]

On February 4, 2013, Spy News Ghana stated that the research findings show that MenAfriVac is safe and can be given to children under one year old, providing long-term protection from Group-A meningococcal meningitis in this age group. [11]

CONCLUSION

Today, the latest news from Gouro is that 40 children remain paralyzed in hospitals in both Chad and Tunisia, and a further 56 remain ill in the village of Gouro. However, news from Ecoterra International on February 9, 2013, said that the new heath minister wants to send them back home to their ill-equipped village. [12]

Until our intervention, there had been no publicity about the serious vaccine injuries in Chad. However, since our articles were published, there has been a flurry of worldwide media attention, including an extremely biased report in the Guardian UK telling the world that MenAfriVac is a wonderful vaccine. Mind you, to be fair, as you will see from the article, The Bill and Melinda Gates Foundation, a well-known supporter of vaccination initiatives, funded this section of the Guardian. [13]

The whole debacle is one coverup after another. The Chadian government has not asked any independent experts to evaluate the safety and efficacy of the MenAfriVac campaign, stirring up anger among the citizens of Chad. They have been left to cope with extremely sick children, many of whom are still reported to be paralyzed and suffering from severe convulsions. The children need appropriate medical care and their parents deserve answers.

Key

CDC – Centers for Disease Control
FDA – Food and Drug Administration
BMGF – The Bill and Melinda Gates Foundation
PATH – Program for Appropriate Technology in Health
MVP – Meningitis Vaccine Project
WHO – World Health Organization
UNICEF – United Nations International Children’s Emergency Funding

 

 

References

1.  http://www.tolerance.ca/Article.aspx?ID=157421&L=en
2.  http://www.sante-tchad.org/Renforcer-les-ressources-humaines-en…
3.  http://vactruth.com/2013/01/13/children-paralyzed-by-vaccine/
4.  http://www.seruminstitute.com/content/products/product_menafrivac.htm
5.  http://www.who.int/immunization_delivery/systems_policy/IPAC_2012_October_report.pdf
6.  http://www.cdc.gov/vaccines/pubs/pinkbook/vac-storage.html#temperatures
7.  http://weatherspark.com/averages/29142/N-Djamena-Chari-Baguirmi-Chad
8.  http://www.treehugger.com/clean-technology/9-countries-have-recorded…
9.  http://www.meningvax.org/clinical-004.php
10. http://www.meningvax.org/files/MVPnewsdigest_2010_Q4_27_EN.pdf
11. http://www.spyghana.com/research-shows-that-new-meningitis-vaccine-is-safe-for-children/
12. http://www.groundreport.com/World/Do-to-them-what-they-are-doing-to-you/2951229
13. http://www.guardian.co.uk/global-development/2013/feb/04/aid-vaccines…

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Multiple vaccine doses have resulted in up to 145,000 child deaths in past 20 years

Thursday, January 24, 2013 by: Jonathan Benson, staff writer

Learn more: http://www.naturalnews.com/038812_vaccines_childhood_deaths_toxic_chemicals.html#ixzz2IuLBfoac

(NaturalNews) The recommended childhood vaccination schedule has changed dramatically over the years, with children now receiving upwards of 30 vaccines, including multiple combination vaccines, before the age of six. And in many cases, doctors and nurses administer half a dozen or more vaccines all at once during a single visit to make sure children get all these shots and to save time. But according to data compiled from the government’s Vaccine Adverse Events Reporting System (VAERS), as many as 145,000 children or more have died throughout the past 20 years as a result of this multiple vaccine dose approach, and few parents are aware of this shocking fact.

In a study recently published in the journal Human & Experimental Toxicology, researchers evaluated the overall number of hospitalizations and deaths associated with vaccines administered between 1990 and 2010, and compared this data to the number of vaccines given at one time to individual children. Hospitalizations and deaths resulting from one vaccine dose were compared to those of two vaccine doses, in other words, and the same all the way up to eight vaccine doses. Researchers also evaluated overall hospitalization and death rates associated with getting one to four combined vaccine doses, five to eight combined vaccine doses, and one to eight combined vaccine doses.

Upon analysis, the team found that the more vaccines a child receives during a single doctor visit, the more likely he or she is to suffer a severe reaction or even die. According to Heidi Stevenson from Gaia Health, for each additional vaccine a child receives, his or her chance of death increases by an astounding 50 percent — and with each additional vaccine dose, chances of having to be hospitalized for severe complications increase two-fold. To sum it all up, the overall size of the vaccine load was found to be directly associated with hospitalization and death risk, illustrating the incredible dangers of administering multiple vaccines at once.

Parents of children who become injured after just one vaccine tend to cease further vaccinations, suggests data

Interestingly, the total number of reported hospitalizations and deaths from getting just one vaccine was higher than the number reported for getting two, three, or even four vaccines. Though the precise reason for this is unknown, it is believed that newborns mostly fall into the one vaccine category, and those that are injured by a single vaccine tend not to get any more vaccines, hence the immediate decrease observed among children who received only two vaccines. Once a child reaches five vaccinations; however, the hospitalization and death rate jumps dramatically, the reason for which was not investigated as part of the study.

“Our findings show a positive correlation between the number of vaccine doses administered and the percentage of hospitalizations and deaths reports to VAERS,” wrote the authors in their conclusion. “In addition, younger infants were significantly more likely than older infants to be hospitalized or die after receiving vaccines. Since vaccines are administered to millions of infants every year, it is imperative that health authorities have scientific data from synergistic toxicity studies on all combinations of vaccines that infants are likely to receive.”

You can view the complete results of the study in their entirety here: http://gaia-health.com

Sources for this article include:

http://gaia-health.com

Learn more: http://www.naturalnews.com/038812_vaccines_childhood_deaths_toxic_chemicals.html#ixzz2IuL6H9Qm

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Polio campaign: was stoppage less dangerous than the vaccine?

Published: January 23, 2013

The writer is a former journalist and currently director of The Green Economic Initiative at Shirkat Gah, a rights and advocacy group najma.sadeque@tribune.com.pk

The Taliban may have hijacked the polio eradication campaign for all the wrong reasons, but that still does not make the programme a desirable one.

The government and other institutions continue with the authoritarian patronage mentality, not feeling it necessary to inform and educate people first so as to enable them to make informed choices. There is an assumption that the powers-that-be always know better, reflecting contempt for the illiterate or less-educated masses — just as government hospital doctors do not bother to explain to patients the nature of their problem, often not even providing the name of the disease they are affected by.

The government has either not kept up with developments surrounding the polio vaccine, or it has chosen not to divulge inconvenient information to the public. Should it not have told us that the oral polio vaccine itself, for example, has also become a carrier of polio? Should we not have been told which vaccine is being used in Pakistan? Is it the newer, ‘inactivated’ risk-free vaccine, which the US and other industrialised countries started using after abandoning the previous one? Or is it based on the original vaccine made from a live poliovirus which carries the risk of transmitting polio — but is still used in Third World countries because it is much cheaper, even though there continue to be outbreaks?

It was the late Dr Maurice Hilleman, developer of Merck’s vaccine programme, who discovered that the new virus had come about via the polio vaccine he had developed. Given that this vaccine is now the leading cause of polio paralysis, it makes one wonder about the real reason this campaign is being thrust on us, complete with threats of not allowing Pakistanis to travel abroad — or even blockade us — if we fail to carry out the programme.

This is certainly a matter for the professionals, and yet, the medical community continues to be inexplicably quiet on the issue. The electronic media needs to look beyond the senselesskillings into the vaccine itself.

A dangerously erroneous impression that prevails is that the oral vaccine alone prevents polio, mainly because the government disseminates little of relevance and would be caught out in its neglect of health infrastructure if it preceded polio campaigns with an information blitz about how polio is caused.

It is important to drive home the message clearly and unambiguously that polio arises from unhygienic conditions. There is only one cause to polio and that is infection through the poliovirus, which infects humans and humans alone. It is extremely contagious and spreads easily from person to person. Specifically, it mostly spreads through contact with the faeces of the infected person, which can be through unwashed hands or inadequately cleaned utensils or clothing or other surfaces touched.

To a lesser extent, it can also spread through infected saliva or respiratory secretions. It is not restricted to any season and in Pakistan’s warm climate and widespread unsanitary conditions, thrives more easily. Infected persons can, therefore, also infect outsiders as they come into contact with them, who otherwise practise very hygienic habits.

It is important to be aware that the live poliovirus enters the intestinal tract and mucus in the nose and throat of infected persons for one to two weeks, or in the faeces for up to two months, according to the Global Vaccine Institute. This makes the rest of the household extremely susceptible, children and adults alike.

If Pakistan really wants to be polio-free, it is more important for governments to spend much, much more on clean water supply and household sanitation, specifically on toilets that are easy to maintain — at least two in every home; one for the men, and the other for women and children. In the bargain, this would help eradicate a whole lot of other water-borne diseases that also affect us.

Without cleanliness, the oral polio vaccine can do very little good. In fact, in a previous round, 78 per cent of Pakistani children, who contracted polio, turned out to be the very ones who had been vaccinated earlier. The Centres for Disease Control (CDC) confirms that it is possible for children to develop polio from the vaccine itself. According to the World Health Organisation (WHO), despite the large percentage of prescribed vaccinations carried out, Pakistan had the highest number of polio cases in a decade.

What is worse, the virus in the vaccine can mutate into deadlier versions. Seemingly, the wild virus is being replaced by the vaccine-derived one, which causes paralysis. Earlier this year, an international meeting was organised by WHO in collaboration with the US Centres for Disease Control and Prevention (CDCP) and the Japanese ministry of health on this matter. Why haven’t we heard the outcome of this?

Meanwhile, those who want to be kept informed and updated for their own protection could sign up with the free online advocacy portal of the National Vaccine Information Centre(NVIC), USA, the world’s leading source on vaccines and infectious diseases. The founder of the NVIC had long ago said that “with mounting evidence that cross-species transfer of viruses can occur, the United States should no longer be using animal tissues to produce vaccines”. Incidentally, NVIC has throughout advocated for informed consent to vaccination, something that our own government or international backers seem to feel differently about.

The fact remains that vaccines don’t work for everyone invariably; they may work for some, but also fail others disastrously. And yet, the authorities were ready to penalise parents in some way or the other if they refused to let their children be vaccinated. Now, they can divert attention and blame it on the Taliban instead. Vaccines by the millions make a lot of money for pharmaceutical companies producing them, but polio is too high an individual or national price to pay for profits.

Published in The Express Tribune, January 24th, 2013.

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Dec 16th, 2012 | By Christina England

A confidential GlaxoSmithKline document recently leaked to the press exposed that within a two-year period, a total of 36 infants died after receiving the 6-in-1 vaccine, Infanrix Hexa. [1] According to the website Initiative Citoyenne [2] who reported the news, the 1271 page document revealed that GlaxoSmithKline received a total of 1,742 reports of adverse reactions between October 23, 2009, and October 22, 2011, including 503 serious adverse reactions and 36 deaths. Initiative Citoyenne stated:

“It’s not that 14 deaths were recorded by GSK between October 2009 and end in October 2011 as we had originally calculated but 36 (14 from 2010 to 2011 and 22 from 2009 to 2010). In addition to these 36 deaths at least 37 other deaths (sudden death mainly), bringing the total to at least 73 deaths since the launch of the vaccine in 2000, and again, this concerns only the death by sudden death, no further recovery of under-reporting.”

Using the figure of 36 deaths over a two-year period, this averages 1.5 deaths per month, which by anyone’s standard is extremely high. Note that only 1 to 10% of adverse reactions to vaccines are actually reported. Therefore, in reality, the problem could potentially be far more serious and the actual number of fatalities much higher.

THE DEADLY CHEMICAL COCKTAIL

The charts show that many of the babies who died passed away within the first few days of receiving the vaccine. [3] A total of three infants were reported to have died within hours of receiving the vaccine. This tragedy is hardly surprising given the vaccine’s ingredients listed on the GSK Infanrix Hexa product information leaflet, which parents are rarely given the chance to read prior to vaccination, including non-infectious substances from tetanus, diphtheria bacteria, purified proteins of pertussis bacteria, the surface protein of the hepatitis B virus (HBsAg, derived from genetically engineered yeast cells) and inactivated poliovirus. [4] Each 0.5mL dose contains:

diphtheria toxoid
tetanus toxoid
pertussis toxoid
filamentous haemagglutinin
pertactin
recombinant HBsAg protein
poliovirus Type 1
poliovirus Type 2
poliovirus Type 3
purified capsular polysaccharide of Hib covalently bound to tetanus toxoid
aluminium hydroxide
aluminium phosphate
2-phenoxyethanol, lactose
Medium 199
neomycin
polymyxin
polysorbate 80
polysorbate 20
sodium chloride
water
TOXIC DOSES OF TOXIC CHEMICALS

In an interesting article by Dr. Harold Buttram titled “The Ultimate Gamble: Do Childhood Vaccines Result in Genetic Hybridization from Alien Human and Animal DNA Contents?” he highlighted the problems associated with just two of these ingredients, including aluminum, which is a neurotoxin associated with Alzheimer’s disease and seizures, and formaldehyde, which is a known cancer-causing agent commonly used to embalm corpses. [5]

Dr. Harold Buttram also stated:

“It is universally recognized among toxicologists that combinations of toxic chemicals may bring exponential increases in toxicity; that is, two toxic chemicals in combination will bring a ten-fold or even a hundred-fold increase in toxicity.

A classical example of this principle was the Schubert study [21] in which it was found that the amount of lead and the amount of mercury, when each was given separately, would be lethal for one percent of rats tested, would become lethal for one hundred percent of rats tested when combined.

In vaccines this principle would apply at least to mercury and aluminum, both of which are potent neurotoxins.”

CONCLUSION

Considering this information, is it any wonder that babies are dying after receiving vaccinations containing these ingredients? GlaxoSmithKline may try and hide the facts from us but they cannot hide them forever. Infanrix Hexa should be removed from the market immediately.

References
Confidential To Regulatory Authorities – Biological Clinical Safety and Pharmacovgilance – GlaxoSmithKline Research and Development Avenue Fleming 20 1300 Wavre Belgium http://ddata.over-blog.com/xxxyyy/3/27/09/71/2012-2013/confid.pdf
Initiative Citoyenne http://ddata.over-blog.com/xxxyyy/3/27/09/71/2012-2013/Communique-de-presse-d-IC-du-6-dec.-2012-_doc-confidentie.pdf
Initiative Citoyenne Charts http://www.initiativecitoyenne.be/article-infanrix-hexa-le-document-confidentiel-accablant-113251207.html
Infanrix Hexa product information leaflet http://www.betterhealth.vic.gov.au/bhcv2/bhcmed.nsf/pages/gwcinfih/$File/gwcinfih.pdf
Dr Harold Buttram The Ultimate Gamble: Do Childhood Vaccines Result in Genetic Hybridization from Alien Human and Animal DNA Contents?” http://vactruth.com/2012/03/13/vaccines-human-animal-dna/

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Study Shows This Amazingly Simple Act Reduces 2 Leading Childhood Diseases by 50% or More!

Dec 29th, 2012 | By Jeffry John Aufderheide | Category: Jeffry John Aufderheide,

Garbage collects outside of a school in Karachi, Pakistan.
It’s not black magic or some out-of-date belief—just good old-fashioned common sense.

Better hygiene, sanitation, and organic food are the foundations for good health. But to what degree could one of those elements (hygiene, for example) have an effect on decreasing a disease? I think finding the answer to this question and considering the evidence is valuable for parents who are considering vaccinating their children.

Why?

Mainstream health officials at the Centers for Disease Control and other such agencies in the United States use emotionally charged language to declare that vaccines—not better sanitation or hygiene— saved the world from deadly diseases.

It is for this reason that I must warn you: Those who push vaccines often trivialize or underestimate the information I am going to share with you. It completely destroys what they have been told for many years.

If you’re interested in learning more, read on.

The Gold Standard

The big secret vaccine peddlers avoid like the plague is, one amazingly simple act reduced two diseases by 50% or more. The most vital point to remember: The decrease in morbidity of—or the rate of incidence of a disease—those affected by the diseases had nothing to do with vaccines!

To get our answer, we turn to Karachi, Pakistan.

In 2002, a randomized controlled trial (a gold standard of scientific research) was performed by Dr. Stephen P. Luby in Karachi, Pakistan. The goal of the study was to assess the impact of hand washing and bathing with soap in settings where infectious diseases are leading causes of childhood disease and death. [1–3]

It is known as the Karachi Health Soap Study.

It’s noteworthy to keep in mind that the variable studied was hand washing—not improved sanitation (waste water treatment), clean drinking water, better food or storage, or even vaccines. In Karachi, sewage contaminates the drinking water and feces contaminates the environment. This is what makes the study so radically powerful!

If you want to see an overview of what was done, read on.

The Power of Simplicity and Education

Here are the some relevant facts you should know about the Karachi Health Soap Study[3]:

25 neighborhoods were either given an antibacterial soap (containing 1.2% triclocarban) or plain soap.
11 neighborhoods were the control. In other words, no hygiene promotion occurred, and no soap was dispensed in these neighborhoods.
Both the antibacterial soap and plain soap looked and smelled identical.
Both types of soap were packaged identically in generic white wrappers. Neither the fieldworkers nor the families knew whether the soaps were antibacterial or plain.
Fieldworkers reviewed with the families the health problems that resulted from contaminated hands and provided them with specific hand-washing instructions.
Fieldworkers encouraged households to wash their hands after defecation, after cleaning an infant who had defecated, before preparing food, before eating, and before feeding infants.
Fieldworkers encouraged participants to bathe once a day with soap and water.
Here’s what happened next…

Dramatic Decrease in Diseases

karachi-statistics

Remember my warning in the beginning of the article about the information being dismissed? As you will see, the results are very dramatic.

As noted by the study, in the first 6 months not much change or variation (only 6%) was noted between the different groups. In the graph below, the biggest change came in the second half of the year.

Source: Karachi Health Soap Study [3]

The results of the study were analyzed after 51 weeks.

Primary diarrhea outcomes in children younger than 15 years by intervention group
Antibacterial soap: 47% fewer incidences of diarrhea than control group
Plain soap: 52% fewer incidences of diarrhea than control group
Primary respiratory outcomes in children younger than 15 years by intervention group
Antibacterial soap: 45% fewer incidences of pneumonia than control group
Plain soap: 50% fewer incidences of pneumonia than control group
It is essential to reemphasize, the World Health Organization lists pneumonia (lower-respiratory infection) and diarrhea as the number 1 and number 2 diseases, which kill more than 3.5 million children worldwide each year. [3–5]

This seems to be in harmony with the principle that Antoine Bechamp—and even Weston Price—wrote about many years ago: The health of the host is everything. The disease is nothing. [6]

Considering that the people in the Karachi study drank the same water, ate the same foods, had the same indoor plumbing (or lack thereof), etc., a significant question has to be asked. If simple hand washing can decrease the morbidity of diarrhea and pneumonia by 50% or more, what happens when better sanitation facilities, food storage, and quality of food are introduced?

Even more important, I’d think there would be comparative data on the effectiveness of hand washing and vaccines. But if that were to happen—given the safety track record of soap versus vaccines—the entire vaccine program would receive a severe death blow.

What we know is when the standard of living increases, mortality and morbidity rates fall.

As an example, mortality rates (not morbidity) in the United States decreased prior to the introduction of vaccines (notice there was not a vaccine for scarlet fever).

What could cause such an intense drop in mortality rates? It obviously wasn’t the vaccines. If vaccines caused a 50% drop in morbidity or mortality rate of a disease within a 6-month period, the media would broadcast it all over the news, singing the praises and benefits of getting injected.

The irony of this study is that the Centers for Disease Control provided some funding and reviewed the data. Here’s an excerpt from the study:

The balance of the funding was provided by the Centers for Disease Control and Prevention. Inclusion of soap trade names is for identification only and does not imply endorsement by CDC or the Department of Health and Human Services. These data were presented in part at the International Conference on Emerging Infectious Diseases, Atlanta, GA, USA, in February, 2004. [3]

So, now you know that some people at the Centers for Disease Control know. But here’s the clincher.

Vaccine Pushers

The Centers for Disease Control recommend the following vaccines in the United States to prevent the very same diseases discussed above.

For diarrhea: RotaTeq® (RV5) and Rotarix® (RV1). [7]

For pneumonia: Pneumococcal, haemophilus influenzae type b (Hib), pertussis (whooping cough), varicella (chickenpox), measles, and influenza (flu) vaccine. [8]

Does the Centers for Disease Control mention washing hands as a means of prevention? Sure—in passing.

They say something to the effect that good hygiene is important, but is not enough to control the spread of the disease. They recommend vaccines.

Then again, you might want to consider why the CDC is so adamant about recommending vaccines. For example, this is from an article on Mercola.com:

Dr. Paul Offit of the Children’s Hospital of Philadelphia earned millions of dollars as part of a $182-million sale by the hospital of its worldwide royalty interest in the Merck Rotateq vaccine … The high price placed on the patents raises concerns over Offit’s use of his former position on the CDC’s Advisory Committee on Immunization Practices (ACIP) to help create the market for rotavirus vaccine— effectively, to vote himself rich. [9]

Could the deep ties to the pharmaceutical companies be the reason the CDC puts more emphasis on vaccines? Considering the evidence presented in the Karachi Health Soap Study, which would you choose—better hygiene or a vaccine?

Conclusion

What’s the moral of the story?

The data revealed by Stephen P. Luby in the Karachi Health Soap Study is nothing short of spectacular. Children who washed their hands and skin with plain soap had 52% less diarrhea and 50% less pneumonia. Good hygiene has a significant impact on decreasing disease, and I think it is something we take for granted in the United States.

Please remember this point: If better nutrition and sanitation were added as components of this or a future study, I suspect that Karachi, Pakistan, would see a more dramatic drop in diseases, much like in the United States—and I would highly encourage such efforts.

Just imagine the implications of a comparative study being performed between hygiene practices and vaccines for decreasing disease. What do you think the outcome would be? My money would be on hygiene practices being the clear winner.

Here’s the shocking reality.

You hold in your hands the real power and master key to good health. It doesn’t come through the tip of a needle.

References

http://en.wikipedia.org/wiki/Randomized_controlled_trial

http://en.wikipedia.org/wiki/Levels_of_evidence

Luby, Stephen P., Mubina Agboatwalla, Daniel R. Feikin, John Painter, Ward Billhimer, Arshad Altaf, and Robert M. Hoekstra.“Effect of Handwashing on Child Health: A Randomised Controlled Trial.” The Lancet 366, no. 9481 (July 16, 2005): 225–233. doi:10.1016/S0140-6736(05)66912-7. http://www.ncbi.nlm.nih.gov/pubmed/16023513
WHO Pneumonia Fact Sheet: http://www.who.int/mediacentre/factsheets/fs331/en/
WHO Diarrhoeal Fact Sheet: http://www.who.int/mediacentre/factsheets/fs330/en/

http://www.naturalnews.com/030384_Louis_Pasteur_disease.html

http://www.cdc.gov/rotavirus/about/prevention.html

http://www.cdc.gov/Features/Pneumonia/

http://articles.mercola.com/sites/articles/archive/2009/06/25/vaccine-doctor-given-at-least-30-million-dollars-to-push-vaccines.aspx

Read Full Post »

Dec 27th, 2012 | By Christina England | Category: Christina England, Recent Articles, Top Stories
1696

Last week, VacTruth reported details of the 1,271 page confidential GlaxoSmithKline document, regarding their six-in-one vaccine. More confidential papers have recently been leaked to the press. The Belgian website Initiative Citoyeene reported both leaked documents.

The latest confidential document concerns the Prevenar 13 vaccine, a pneumococcal vaccine manufactured by Pfizer (now merged with Wyeth). [1] This vaccine replaced the original 2010 vaccine Prevenar, which, as reported by the manufacturer, has actually increased, rather than decreased, serious infections.

The Prevenar 13 protects infants against Streptococcus pneumoniae bacteria which can lead to cases of meningitis, bacteraemia (an infection of the blood), pneumonia and ear infections. [2] It is usual for the six-in-one vaccination Infanrix Hexa and the Prevenar 13 vaccine to be administered to small babies at the same time.

According to the leaked confidential Wyeth (Pfizer) documents and a reply from the European Medicines Agency (EMA), both the manufacturer and the agency are aware of a significantly higher number of adverse neurological events in children vaccinated with both Prevenar 13 AND Infanrix Hexa, as per the Belgian vaccination schedule at ages two months and four months.

THE FIRST SET OF LEAKED DOCUMENTS

First, let’s revisit the leaked confidential document regarding the Infanrix Hexa vaccine information, which I revealed just days ago on VacTruth. I exposed a hidden GlaxoSmithKline document that had been leaked to the press, revealing 36 infant deaths. [3]

The document, titled Confidential To Regulatory Authorities Infanrix Hexa Summary Bridging Report [4] stated that between October 23, 2009, and October 22, 2011, GlaxoSmithKline received a total of 1,742 reports of adverse events, including 503 serious adverse events, after children had received the 6 in 1 vaccine, Infanrix Hexa.

(Infanrix Hexa is a 6-in-1 vaccination, which combines the Combined Diphtheria, Tetanus and Acellular Pertussis, Hepatitis B enhanced Inactivated Poliomyelitis and the Haemophilus influenzae type B vaccine. It is used in 92 countries worldwide.)

The GlaxoSmithKline confidential document detailed each and every one of the 1,742 adverse events. The list was so long, it required a full twenty pages. Here are some of the adverse events detailed on charts between pages 11 and 31 of their document:

106 cases of cyanosis

69 cases of loss of consciousness

165 cases of hypotonia

102 cases of hypotonic-hyporesponsive episodes

107 cases of convulsions

20 cases of epilepsy

98 cases of febrile convulsions

33 cases of grand mal convulsions

47 apnea attacks

108 cases of vomiting

43 cases of Gaze Palsy

12 cases of anemia

1 case of bone marrow failure

6 cases of cardiac arrests

53 cases of diarrhea

593 cases of pyrexia (high temperature)

22 cases of gait disturbance

6 cases of anaphylaxis

62 cases of pertussis (whooping cough)

2 cases of meningitis pneumococcal

3 cases of arthritis

16 cases of muscle twitching

22 cases of tremors

264 cases of crying (does not indicate the severity)

2 cases of Guillain-Barre syndrome

10 cases of respiratory arrest

7 cases of Kawasaki’s disease

All of these adverse events occurred after the child received the Infanrix Hexa vaccination, some just hours after being vaccinated. I am sure you will agree that these documented facts make extremely uncomfortable reading.

However, if this information is not disturbing enough, in the document, GlaxoSmithKline revealed on page twenty a total of 68 cases of vaccination failure! This fact proves that, not only does their vaccine appear to cause death, injury and illness in multiple children, but that this vaccine failed to give any “protection” at all to at least 68 children.

The document was signed by Safety Scientist Vanessa Corman and Vice President, Lead Biological Clinical Safety and Pharmacovigilance Dr. Felix Arellano, M.D., from GlaxoSmithKline Biologicals.

THE SECOND SET OF LEAKED DOCUMENTS

Now, let’s continue with the shocking new papers that the Belgian website Initiative Citoyeene have revealed. They stated:

“On the 4th of January this year, at the end of the required 6-week period, two Pfizer Group Regulatory Affairs Directors, Mary Allin and Helen Edwards, sent a response to Dr. S. Spinosa of the European Medicine Agency on the topic of ‘higher number of neurologic events reported in Italy following the coadministration of Pevenar 13 and hexavalent vaccines.’ The two directors specified at the end of this letter that based on data supplied, they did not feel there was any need to modify the vaccine’s reference safety information (RSI), in other words, its package insert.”

So, let’s take a closer look at one of the confidential reports that Initiative Citoyenne has been quoting. This confidential document reveals that over a two-year period, 22 deaths were reported, representing 2.6% of the total number of cases and a total of 51 reported cases of lack of efficacy, or vaccination failure! [4]

BRAIN DAMAGE AND DEATH

The next section relates to reports of neurological events.

The Master of Health Administration (MAH), was asked by the Committee for Medicinal Products for Human Use (CHMP), to provide a cumulative review of neurological reactions in those cases, which were reported to have received Prevenar 13 concomitantly (at the same time) with hexavalent (6-in-1) vaccine.

The MAH reported that during the two-year period between July 10, 2009, and July 9, 2011, a total of 1,691 cases of adverse events were reported after the Prevenar 13 vaccine. Of those adverse events, 312 cases (18%) were indicative of neurological reactions. [5] The 1,691 cases were then divided in three different datasets. The Initiative Citoyenne website explained the findings:

“An important fact is that Pfizer assessed the respective frequency of neurologic accidents in three different groups of children: those who had all received only the Prevenar 13 on the same day, those who had received both the Prevenar 13and other vaccines on the same day and those who had received both the Prevenar 13 and a hexavalent vaccine on the same day.

Of the 934 children who had only received the Prevenar 13 and experienced adverse effects, 87 displayed neurologic events (87/934 = 9%).

Of the 287 children who had received the Prevenar 13 plus other vaccines on the same day, and experienced adverse effects, 62 had had neurologic episodes (62/287 = 21%).

Of the 470 children who received the Prevenar 13 plus a hexavalent vaccine, on the same day, and reported adverse effects, 163 had experienced neurologic reactions (163/470 = 34%!!). It is therefore clear that the concomitant administration of several vaccines, particularly those recommended in the Belgian vaccine schedule (Prevenar 13 alongside Infanrix Hexa), multiplies the risk of neurologic reactions including serious and potentially irreversible adverse events!”

To describe the enormity of the situation, they further stated, in easy-to-understand terms:

“To grasp the extent of the problem, just remember that the Belgian annual birth rate is approximately 128,000, a very large majority of whom receive BOTH the Prevenar and the Infanrix Hexa. A simple calculation reveals therefore that the annual number of serious adverse effects, taking ONLY this vaccine into account, could be 3% x 128,000 births = 3,840 children!”

MORE REASONS TO AVOID THIS SIX-IN-ONE VACCINE

Interestingly, the Prevenar 13 leaflet mentioned earlier states reasons why your child should not be given Prevenar 13:

“Your child should not have Prevenar 13 if he or she has ever had an allergic reaction to pneumococcal or DIPTHERIA VACCINES, or any of the ingredients listed at the end of this leaflet.”

Despite this warning, the Prevenar 13 vaccine is often given at the same time the Infanrix Hexa vaccine, which includes a diptheria component! These vaccines are recommended from as early as six weeks of age, according to the leaflet, at which time a parent would not know whether their child was allergic to the diptheria component or not.

One Belgian child who lost her life as a consequence of being given several vaccinations in one visit, which included the Infanrix Hexa vaccine together with Prevenar, was Stacy Sirjacobs. Stacy was an eight week-old premature twin who died in December 2011. [6]

These vaccines were given to Stacy despite advice given by the European Medicines Agency in their ANNEX I SUMMARY OF PRODUCT CHARACTERISTICS for Infanrix Hexa report which stated:

“When Infanrix Hexa is co-administered with Prevenar (pneumococcal saccharide conjugated vaccine, adsorbed), the physician should be aware that data from clinical studies indicate that the rate of febrile reactions was higher compared to that occurring following the administration of Infanrix Hexa alone.”
[7]

Furthermore, the document contained information about administering the vaccine to premature infants:

“Limited data in 169 premature infants indicate that Infanrix Hexa can be given to premature children. However, a lower immune response may be observed and the level of clinical protection remains unknown.

The potential risk of apnea and the need for respiratory monitoring for 48-72h should be considered when administering the primary immunisation series to very premature infants (born ≤ 28 weeks of gestation) and particularly for those with a previous history of respiratory immaturity.”

TROUBLING QUESTIONS

The European Medicines Agency offered warnings about administering the vaccine concomitantly with another vaccine and cautioned health care providers to consider the additional risks of vaccinating premature infants. Then why was little Stacy, a baby born one month prematurely, delivered by Caesarean section, resuscitated at birth, who spent the next four days in an incubator, given these vaccinations and then sent home without any extra advice?

Her death was a tragedy, yet babies are still dying and being neurologically damaged on a regular basis. The proof is in the manufacturer’s report in black and white. The drug companies know, the regulatory agencies know and worse still, our governments know.

Slowly, day-by-day, the depth of their corruption is being uncovered. Parents are not being told the truth, they are being deceived and lied to and the price they pay is extremely high.

CONCLUSION

These adverse events were being reported as far back as 2009. So, why are these two vaccines still being recommended for babies as young as 6 weeks old? Surely, the most sensible and responsible action would be for the manufacturers GlaxoSmithKline and Pfizer to suspend the use of these vaccines until their use can be shown to be reliable, effective, and safe. Instead, this information is being hidden from the public.

Furthermore, the mainstream media is so quiet you could hear a pin drop. Dr. Rebecca Carley, an expert specializing vaccine-induced diseases syndromes, has often stated on her radio shows that vaccinations are the ‘True Weapons of Mass Destruction,” and the evidence contained in these leaked, confidential documents shows she could be right.

Acknowledgements

The author would like to thank the website Initiative Citoyenne for bravely revealing the truth.

The staff at VacTruth wishes to express their heartfelt condolences to the family of Stacy Sirjacobs and other families whose children have suffered injuries or death following vaccination.

References
Initiative Citoyenne Press Release http://ddata.over-blog.com/3/27/09/71/2012-2013…
Prevenar 13 leaflet Consumer Medical Information http://www.nps.org.au/__data/assets…

http://vactruth.com/2012/12/16/36-infants-dead-after-vaccine/

Confidential To Regulatory Authorities Infanrix TM hexa Summary Bridging Reporthttp://ddata.over-blog.com/3/27/09/71/2012-2013/confid.pdf
Prevenar 13 PSUR 04 – Response to RSI Neurological Events PFIZER CONFIDENTIAL Page 1 Prevenar 13 Pneumococcal saccharide conjugated vaccine, 13 valent adsorbed PSUR 04 – Response to Question on Neurological events http://ddata.over-blog.com/xxxyyy/3/27/09/71/2012-2013/emea-responses–Prevenar-13-Pfizer-Confidential.pdf

http://vactruth.com/2012/01/19/baby-dies-after-first-shots/

European Medicines Agency ANNEX I SUMMARY OF PRODUCT CHARACTERISTICS for Infranrix Hexa http://www.ema.europa.eu/docs/en_GB/document_library…

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To: “admin@thejamiat.co.za” , Kerstin Sami , Laila Brence , “m \”mughiss\”" , Maryam Asif , “muftis@themajlis.net” , saifuddin1979 , samun , “samuslims@samuslims.co.za” , “The Mujlisul Ulama of South Africa M.U.S.A” , “The Mujlisul Ulama of South Africa M.U.S.A” , wajiha_ahmad , Zahida Oumadam , mhd_ahmad@yahoo.com, ayesha malik , Hassan Sulaiman , muhammad_taqi@cyber.net.pk, darulifta@gmail.com, darulolumkhi@hotmail.com, darulolumkhi@wtmeca.net, binoria@binoria.org, Abd Muhtaj
Cc:
Date: Fri, 11 Jan 2013 17:07:33 +0500
Subject: 1,742 Reports of Adverse Events After Children Received This Vaccine
1,742 Reports of Adverse Events After Children Received This Vaccine

Dec 27th, 2012 | By Christina England | Category: Christina England, Recent Articles, Top Stories
1696

3
inShare
Last week, VacTruth reported details of the 1,271 page confidential GlaxoSmithKline document, regarding their six-in-one vaccine. More confidential papers have recently been leaked to the press. The Belgian website Initiative Citoyeene reported both leaked documents.

The latest confidential document concerns the Prevenar 13 vaccine, a pneumococcal vaccine manufactured by Pfizer (now merged with Wyeth). [1] This vaccine replaced the original 2010 vaccine Prevenar, which, as reported by the manufacturer, has actually increased, rather than decreased, serious infections.

The Prevenar 13 protects infants against Streptococcus pneumoniae bacteria which can lead to cases of meningitis, bacteraemia (an infection of the blood), pneumonia and ear infections. [2] It is usual for the six-in-one vaccination Infanrix Hexa and the Prevenar 13 vaccine to be administered to small babies at the same time.

According to the leaked confidential Wyeth (Pfizer) documents and a reply from the European Medicines Agency (EMA), both the manufacturer and the agency are aware of a significantly higher number of adverse neurological events in children vaccinated with both Prevenar 13 AND Infanrix Hexa, as per the Belgian vaccination schedule at ages two months and four months.

THE FIRST SET OF LEAKED DOCUMENTS

First, let’s revisit the leaked confidential document regarding the Infanrix Hexa vaccine information, which I revealed just days ago on VacTruth. I exposed a hidden GlaxoSmithKline document that had been leaked to the press, revealing 36 infant deaths. [3]

The document, titled Confidential To Regulatory Authorities Infanrix Hexa Summary Bridging Report [4] stated that between October 23, 2009, and October 22, 2011, GlaxoSmithKline received a total of 1,742 reports of adverse events, including 503 serious adverse events, after children had received the 6 in 1 vaccine, Infanrix Hexa.

(Infanrix Hexa is a 6-in-1 vaccination, which combines the Combined Diphtheria, Tetanus and Acellular Pertussis, Hepatitis B enhanced Inactivated Poliomyelitis and the Haemophilus influenzae type B vaccine. It is used in 92 countries worldwide.)

The GlaxoSmithKline confidential document detailed each and every one of the 1,742 adverse events. The list was so long, it required a full twenty pages. Here are some of the adverse events detailed on charts between pages 11 and 31 of their document:

106 cases of cyanosis

69 cases of loss of consciousness

165 cases of hypotonia

102 cases of hypotonic-hyporesponsive episodes

107 cases of convulsions

20 cases of epilepsy

98 cases of febrile convulsions

33 cases of grand mal convulsions

47 apnea attacks

108 cases of vomiting

43 cases of Gaze Palsy

12 cases of anemia

1 case of bone marrow failure

6 cases of cardiac arrests

53 cases of diarrhea

593 cases of pyrexia (high temperature)

22 cases of gait disturbance

6 cases of anaphylaxis

62 cases of pertussis (whooping cough)

2 cases of meningitis pneumococcal

3 cases of arthritis

16 cases of muscle twitching

22 cases of tremors

264 cases of crying (does not indicate the severity)

2 cases of Guillain-Barre syndrome

10 cases of respiratory arrest

7 cases of Kawasaki’s disease

All of these adverse events occurred after the child received the Infanrix Hexa vaccination, some just hours after being vaccinated. I am sure you will agree that these documented facts make extremely uncomfortable reading.

However, if this information is not disturbing enough, in the document, GlaxoSmithKline revealed on page twenty a total of 68 cases of vaccination failure! This fact proves that, not only does their vaccine appear to cause death, injury and illness in multiple children, but that this vaccine failed to give any “protection” at all to at least 68 children.

The document was signed by Safety Scientist Vanessa Corman and Vice President, Lead Biological Clinical Safety and Pharmacovigilance Dr. Felix Arellano, M.D., from GlaxoSmithKline Biologicals.

THE SECOND SET OF LEAKED DOCUMENTS

Now, let’s continue with the shocking new papers that the Belgian website Initiative Citoyeene have revealed. They stated:

“On the 4th of January this year, at the end of the required 6-week period, two Pfizer Group Regulatory Affairs Directors, Mary Allin and Helen Edwards, sent a response to Dr. S. Spinosa of the European Medicine Agency on the topic of ‘higher number of neurologic events reported in Italy following the coadministration of Pevenar 13 and hexavalent vaccines.’ The two directors specified at the end of this letter that based on data supplied, they did not feel there was any need to modify the vaccine’s reference safety information (RSI), in other words, its package insert.”

So, let’s take a closer look at one of the confidential reports that Initiative Citoyenne has been quoting. This confidential document reveals that over a two-year period, 22 deaths were reported, representing 2.6% of the total number of cases and a total of 51 reported cases of lack of efficacy, or vaccination failure! [4]

BRAIN DAMAGE AND DEATH

The next section relates to reports of neurological events.

The Master of Health Administration (MAH), was asked by the Committee for Medicinal Products for Human Use (CHMP), to provide a cumulative review of neurological reactions in those cases, which were reported to have received Prevenar 13 concomitantly (at the same time) with hexavalent (6-in-1) vaccine.

The MAH reported that during the two-year period between July 10, 2009, and July 9, 2011, a total of 1,691 cases of adverse events were reported after the Prevenar 13 vaccine. Of those adverse events, 312 cases (18%) were indicative of neurological reactions. [5] The 1,691 cases were then divided in three different datasets. The Initiative Citoyenne website explained the findings:

“An important fact is that Pfizer assessed the respective frequency of neurologic accidents in three different groups of children: those who had all received only the Prevenar 13 on the same day, those who had received both the Prevenar 13and other vaccines on the same day and those who had received both the Prevenar 13 and a hexavalent vaccine on the same day.

Of the 934 children who had only received the Prevenar 13 and experienced adverse effects, 87 displayed neurologic events (87/934 = 9%).

Of the 287 children who had received the Prevenar 13 plus other vaccines on the same day, and experienced adverse effects, 62 had had neurologic episodes (62/287 = 21%).

Of the 470 children who received the Prevenar 13 plus a hexavalent vaccine, on the same day, and reported adverse effects, 163 had experienced neurologic reactions (163/470 = 34%!!). It is therefore clear that the concomitant administration of several vaccines, particularly those recommended in the Belgian vaccine schedule (Prevenar 13 alongside Infanrix Hexa), multiplies the risk of neurologic reactions including serious and potentially irreversible adverse events!”

To describe the enormity of the situation, they further stated, in easy-to-understand terms:

“To grasp the extent of the problem, just remember that the Belgian annual birth rate is approximately 128,000, a very large majority of whom receive BOTH the Prevenar and the Infanrix Hexa. A simple calculation reveals therefore that the annual number of serious adverse effects, taking ONLY this vaccine into account, could be 3% x 128,000 births = 3,840 children!”

MORE REASONS TO AVOID THIS SIX-IN-ONE VACCINE

Interestingly, the Prevenar 13 leaflet mentioned earlier states reasons why your child should not be given Prevenar 13:

“Your child should not have Prevenar 13 if he or she has ever had an allergic reaction to pneumococcal or DIPTHERIA VACCINES, or any of the ingredients listed at the end of this leaflet.”

Despite this warning, the Prevenar 13 vaccine is often given at the same time the Infanrix Hexa vaccine, which includes a diptheria component! These vaccines are recommended from as early as six weeks of age, according to the leaflet, at which time a parent would not know whether their child was allergic to the diptheria component or not.

One Belgian child who lost her life as a consequence of being given several vaccinations in one visit, which included the Infanrix Hexa vaccine together with Prevenar, was Stacy Sirjacobs. Stacy was an eight week-old premature twin who died in December 2011. [6]

These vaccines were given to Stacy despite advice given by the European Medicines Agency in their ANNEX I SUMMARY OF PRODUCT CHARACTERISTICS for Infanrix Hexa report which stated:

“When Infanrix Hexa is co-administered with Prevenar (pneumococcal saccharide conjugated vaccine, adsorbed), the physician should be aware that data from clinical studies indicate that the rate of febrile reactions was higher compared to that occurring following the administration of Infanrix Hexa alone.”
[7]

Furthermore, the document contained information about administering the vaccine to premature infants:

“Limited data in 169 premature infants indicate that Infanrix Hexa can be given to premature children. However, a lower immune response may be observed and the level of clinical protection remains unknown.

The potential risk of apnea and the need for respiratory monitoring for 48-72h should be considered when administering the primary immunisation series to very premature infants (born ≤ 28 weeks of gestation) and particularly for those with a previous history of respiratory immaturity.”

TROUBLING QUESTIONS

The European Medicines Agency offered warnings about administering the vaccine concomitantly with another vaccine and cautioned health care providers to consider the additional risks of vaccinating premature infants. Then why was little Stacy, a baby born one month prematurely, delivered by Caesarean section, resuscitated at birth, who spent the next four days in an incubator, given these vaccinations and then sent home without any extra advice?

Her death was a tragedy, yet babies are still dying and being neurologically damaged on a regular basis. The proof is in the manufacturer’s report in black and white. The drug companies know, the regulatory agencies know and worse still, our governments know.

Slowly, day-by-day, the depth of their corruption is being uncovered. Parents are not being told the truth, they are being deceived and lied to and the price they pay is extremely high.

CONCLUSION

These adverse events were being reported as far back as 2009. So, why are these two vaccines still being recommended for babies as young as 6 weeks old? Surely, the most sensible and responsible action would be for the manufacturers GlaxoSmithKline and Pfizer to suspend the use of these vaccines until their use can be shown to be reliable, effective, and safe. Instead, this information is being hidden from the public.

Furthermore, the mainstream media is so quiet you could hear a pin drop. Dr. Rebecca Carley, an expert specializing vaccine-induced diseases syndromes, has often stated on her radio shows that vaccinations are the ‘True Weapons of Mass Destruction,” and the evidence contained in these leaked, confidential documents shows she could be right.

Acknowledgements

The author would like to thank the website Initiative Citoyenne for bravely revealing the truth.

The staff at VacTruth wishes to express their heartfelt condolences to the family of Stacy Sirjacobs and other families whose children have suffered injuries or death following vaccination.

References
Initiative Citoyenne Press Release http://ddata.over-blog.com/3/27/09/71/2012-2013…
Prevenar 13 leaflet Consumer Medical Information http://www.nps.org.au/__data/assets…

http://vactruth.com/2012/12/16/36-infants-dead-after-vaccine/

Confidential To Regulatory Authorities Infanrix TM hexa Summary Bridging Reporthttp://ddata.over-blog.com/3/27/09/71/2012-2013/confid.pdf
Prevenar 13 PSUR 04 – Response to RSI Neurological Events PFIZER CONFIDENTIAL Page 1 Prevenar 13 Pneumococcal saccharide conjugated vaccine, 13 valent adsorbed PSUR 04 – Response to Question on Neurological events http://ddata.over-blog.com/xxxyyy/3/27/09/71/2012-2013/emea-responses–Prevenar-13-Pfizer-Confidential.pdf

http://vactruth.com/2012/01/19/baby-dies-after-first-shots/

European Medicines Agency ANNEX I SUMMARY OF PRODUCT CHARACTERISTICS for Infranrix Hexa http://www.ema.europa.eu/docs/en_GB/document_library…

Read Full Post »

Secret government documents reveal vaccines to be a total hoax

Tuesday, January 08, 2013 by: Ethan A. Huff, staff writer

(NaturalNews) If you have children, you are more than likely already aware of the official U.S. Centers for Disease Control and Prevention (CDC) “Immunization Schedules,” which today recommend an astounding 29 vaccines be given between birth and six years of age, including yearly flu shots, as well as another five to 16 vaccines between ages seven and 18 (http://www.cdc.gov/vaccines/schedules/). But a recent investigative report compiled by Dr. Lucija Tomljenovic, Ph.D., uncovers more than 30 years of hidden government documents exposing these vaccine schedules as a complete hoax, not to mention the fraud of the vaccines themselves to provide any real protection against disease.

Though her paper focuses primarily on the British health system’s elaborate cover-up of the dirty truth about its own national vaccination program, the tenets of the study’s findings still apply to vaccination schedules in general, which are typically designed for the purpose of serving corporate interests rather than public health. Government authorities, it turns out, in an ongoing bid to satisfy the private goals of the vaccine industry, have deliberately covered up pertinent information about the dangers and ineffectiveness of vaccines from parents in order to maintain a high rate of vaccination compliance. And in the process, they have put countless millions of children at risk of serious side effects and death.

You can access Dr. Tomljenovic’s full paper here:

http://www.ecomed.org.uk/wp-content/uploads/2011/09/3-tomljenovic.pdf

Hiding the truth and covering up data to encourage vaccine compliance

Through several Freedom of Information Act (FOIA) requests, Dr. Tomljenovic was able to obtain transcripts of private meetings that were held between the Joint Committee on Vaccination and Immunization (JCVI), a so-called “independent expert advisory committee” that makes recommendations to the government about vaccine policy, and various British health ministers over the years. And after poring through this plethora of information, which had previously been veiled from public view, Dr. Tomljenovic made some disturbing discoveries.

“[T]he JCVI (Joint Committee on Vaccination and Immunization) made continuous efforts to withhold critical data on severe adverse reactions and contraindications to vaccinations to both parents and health practitioners in order to reach overall vaccination rates which they deemed were necessary for ‘herd immunity,’ a concept which … does not rest on solid scientific evidence,” explains Dr. Tomljenovic in the introduction to her paper.

“Official documents obtained from the U.K. Department of Health (DH) and the JCVI reveal that the British health authorities have been engaging in such practice for the last 30 years, apparently for the sole purpose of protecting the national vaccination program.”

These are some strong accusations, but the information Dr. Tomljenovic gathered speaks for itself. Not only did the JCVI routinely ignore questions of safety as they came up with regards to the ever-expanding vaccination schedule, but the group actively censored unfavorable data that shed a “negative” light on vaccines in order to maintain the illusion that vaccines are safe and effective. Beyond this, the JCVI regularly lied to both the public and government authorities about vaccine safety in order to ensure that people continued to vaccinate their kids.

You can access Dr. Tomljenovic’s full paper here:

http://www.ecomed.org.uk/wp-content/uploads/2011/09/3-tomljenovic.pdf

JCVI was fully aware of MMR vaccine dangers as early as 1989, but covered them up

Beginning on page three of her report, Dr. Tomljenovic begins outlining the sordid details of meetings held as early as 1981 where the JCVI clearly engaged in fraud, cover-up, and lies about vaccines to protect the vaccine industry, not children, from harm. Minutes from these meetings reveal that the JCVI actively tried to cover up severe side effects associated with common vaccines like measles and whooping cough (pertussis), both of which were clearly linked at the time to causing severe brain damage in a substantial percentage of the children that received them.

Of particular concern was how the JCVI handled unfavorable data on the controversial MMR vaccine for measles, mumps, and rubella. 10 years before Dr. Andrew Wakefield published his study on MMR inThe Lancet, JCVI was already fully aware that the National Institute for Biological Standards and Control (NIBSC) had identified a clear link between MMR and vaccine-induced meningitis and encephalitis. But rather than come forward with this information and call for further safety assessments on the vaccine, the JCVI instead censored this critical information from the public, and blatantly lied about the safety of MMR for years.

“The extent of the JCVI’s concerns with the implications of scientific assessment of vaccine safety on vaccine policy explains why they were opposed to any long-term surveillance for severe neurological disorders following vaccination,” writes Dr. Tomljenovic. “[I]nstead of re-evaluating the vaccination policy, at least until safety concerns were fully evaluated, the JCVI chose to support the existing policy based on incomplete evidence that was available at that time.”

In other words, the JCVI was more concerned with protecting the reputation of the dangerous MMR vaccine, as well as many other questionable vaccines, than with protecting children from sustaining serious injuries as a result of getting the jabs. As far as the MMR vaccine is concerned, this critical piece of information not only reinforces the legitimacy of Dr. Wakefield’s findings from 10 years later, which were illegitimately declared to be fraudulent by the establishment, but also illustrates just how painfully long this scam has been taking place.

Vaccine companies urged to manipulate data sheets, skew safety studies to promote vaccines

If this is not bad enough, Dr. Tomljenovic also drudged up copious amounts of information on the JCVI’s longtime habit of encouraging vaccine companies to deliberately alter their data sheets in order to make dangerous and ineffective vaccines appear safe and effective, in accordance with their recommendations. When the JCVI’s guidance contraindications for MMR, for instance, did not match those of the vaccine’s manufacturer, JCVI apparently instructed the manufacturer to alter its data sheets to avoid “legal problems.”

Similarly, the JCVI’s official policy was to cherry-pick unreliable studies to support its own opinions on vaccines rather than rely on independent, scientifically-sound studies to make vaccine policy recommendations. Once again, the JCVI’s position on the safety and effectiveness of MMR is an excellent example of this, as the group flat out ignored legitimate MMR studies in favor of industry-backed junk studies like the infamous 2005 Cochrane Review, which technically proves nothing about the alleged safety of MMR because the 31 studies it evaluated did not even meet the group’s basic methodological criteria.

“Over the years, the JCVI has consistently promoted the MMR vaccine as safe, based on studies that have been proven to be either irrelevant, inconclusive, or methodologically questionable,” explains Dr. Tomljenovic, adding that the JCVI routinely chose to rely on flawed epidemiological studies that only identified “association” rather than “causation,” a rather ironic inaccuracy in light of how scrutinizing the establishment typically is of studies that contradict its own positions.

The eye-opening, 45-page paper goes on to explain how vaccine schedules were established through the calculated downplaying of vaccine safety concerns and the over-inflating of vaccine benefits; the promotion of dangerous new vaccines into the pediatric schedule through deception; the discouraging of vaccine safety follow-up studies; and the widespread brainwashing of the public through manipulation and scientific sleight-of-hand tricks.

Be sure to check out the complete study for yourself:

http://www.ecomed.org.uk/wp-content/uploads/2011/09/3-tomljenovic.pdf

Sources for this article include:

http://childhealthsafety.wordpress.com

http://foodfreedomgroup.com

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Assalaamu alaykum.

Below is a booklet for free to show the Stance of the Ulema e Haqq reagarding the Permissebility of Vaccination! Please read it and forward it.

Wa salaam

Vaccination Devils Medicine BookletERead

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From AbundantHope.net
HEALTH AND NUTRITION
The Vaccine Hoax is Over – Secret Documents Reveal Shocking Truth
By endalldisease.com
Dec 12, 2012 – 2:07:49 AM

The Vaccine Hoax is Over – Secret Documents Reveal Shocking Truth

Freedom of Information Act in the UK filed by a doctor there has revealed 30 years of secret official documents showing that government experts have

1. Known the vaccines don’t work
2. Known they cause the diseases they are supposed to prevent
3. Known they are a hazard to children
4. Colluded to lie to the public
5. Worked to prevent safety studies

Those are the same vaccines that are mandated to children in the US.

Educated parents can either get their children out of harm’s way or continue living inside one of the largest most evil lies in history, that vaccines – full of heavy metals, viral diseases, mycoplasma, fecal material, DNA fragments from other species, formaldehyde, polysorbate 80 (a sterilizing agent) – are a miracle of modern medicine.

Freedom of Information Act filed in the US with the CDC by a doctor with an autistic son, seeking information on what the CDC knows about the dangers of vaccines, had by law to be responded to in 20 days. Nearly 7 years later, the doctor went to court and the CDC argued it does not have to turn over documents. A judge ordered the CDC to turn over the documents on September 30th, 2011.

On October 26, 2011, a Denver Post editorial expressed shock that the Obama administration, after promising to be especially transparent, was proposing changes to the Freedom of Information Act that would allow it to go beyond declaring some documents secret and to actually allow government agencies (such as the CDC) to declare some document “non-existent.”

Simultaneous to this on-going massive CDC cover up involving its primary “health” not recommendation but MANDATE for American children, the CDC is in deep trouble over its decades of covering up the damaging effects of fluoride and affecting the lives of all Americans, especially children and the immune compromised. Lawsuits are being prepared.  Children are ingesting 3-4 times more fluoride by body weight as adults and “[t]he sheer number of potentially harmed citizens — persons with dental fluorosis, kidney patients tipped into needing dialysis, diabetics, thyroid patients, etc — numbers in the millions.”

The CDC is obviously acting against the health of the American people. But the threat to the lives of the American people posed by the CDC’s behavior does not stop there. It participated in designed pandemic laws that are on the books in every state in the US, which arrange for the government to use military to force unknown, untested vaccines, drugs, chemicals, and “medical” treatments on the entire country if it declares a pandemic emergency.

The CDC’s credibility in declaring such a pandemic emergency is non-existent, again based on Freedom of Information Act. For in 2009, after the CDC had declared the H1N1 “pandemic,” the CDC refused to respond to Freedom of Information Act filed by CBS News and the CDC also attempted to block their investigation.  What the CDC was hiding was its part in one of the largest medical scandals in history, putting out wildly exaggerated data on what it claimed were H1N1 cases, and by doing so, created the false impression of a “pandemic” in the US.

The CDC was also covering up e financial scandal to rival the bailout since the vaccines for the false pandemic cost the US billions. And worse, the CDC put pregnant women first in line for an untested vaccine with a sterilizing agent, polysorbate 80, in it. Thanks to the CDC,  “the number of vaccine-related “fetal demise” reports increased by 2,440 percent in 2009 compared to previous years, which is even more shocking than the miscarriage statistic [700% increase].

The exposure of the vaccine hoax is running neck and neck with the much older hoax of a deadly 1918-19 flu. It was aspirin  that killed people in 1918-19, not a pandemic flu. It was the greatest industrial catastrophe in human history with 20-50 million people dying but it was blamed on a flu. The beginning of the drug industry began with that success (and Monsanto was part of it). The flu myth was used by George Bush to threaten the world with “another pandemic flu that could kill millions” – a terror tactic to get pandemic laws on the books in every state and worldwide. Then the CDC used hoax of the pandemic hoax to create terror over H1N1 and to push deadly vaccines on the public, killing thousands of unborn children and others.  (CDC will not release the data and continues to push the same vaccine.)

The hoax of the vaccine schedule is over, exposed by FOIAs in the UK.

The hoax of the CDC’s interest in children’s lives has been exposed by its refusal to respond to a doctor’s FOIAs around its knowledge of vaccine dangers.

The 1918-19 pandemic hoax has been exposed by Dr. Karen Starko’s work on aspirin’s role in killing people.

And despite refusing to respond to FOIAS, the CDC’s scandalous hoax of a 2009 flu pandemic and its part in creating it, was exposed by CBS NEWS.

And the Obama administration, in attempting to salvage the last vestige of secrecy around what is really happening with vaccines, by declaring agency documents non-existent, has made its claim of transparency, non-existent.

But pandemic laws arranging for unknown vaccines to be forced on the entire country are still in place with HHS creating a vaccine mixture that should never be used on anyone and all liability for vaccines having been removed. Meanwhile, a Canadian study has just proven that the flu vaccine containing the H1N1 vaccine which kills babies in utero, actually increases the risk of serious pandemic flu.

Americans who have been duped into submitting their children to the CDC’s deadly vaccines, have a means to respond now. People from every walk of life and every organization, must:

1. take the information from the UK FOIAs exposing 30 years of vaccine lies, the refusal of the CDC to provide any information on what it knows about those lies, and the Obama Administration’s efforts to hide the CDC’s awareness of those lies, and go to their state legislatures, demand the immediate nullification of the CDC vaccine schedule and the pandemic laws.

2. inform every vet. active duty military person, law enforcement people, DHS agents and medical personnel they know, of the vaccine hoax, for their families are deeply threatened, too, but they may not be aware of it or that they have been folded into agency structures by the pharmaceutical industry (indistinguishable from the bankers and oil companies) that would make them agents of death for their country with the declaration of a “pandemic” emergency or “bio-terrorist” attack. It is completely clear now that the terrorism/bioterrorism structures are scams so that any actions taken to “protect” this country using those laws would in fact be what threatens the existence of Americans.

It was aspirin that killed millions in 1918-19.  Now it is mandated and unknown, untested vaccines with banned adjuvants in them that threaten the country with millions of deaths.  At the same time, the CDC is holding 500,000 mega-coffins, built to be incinerated, on its property outside Atlanta.  Not to put to fine a point on this, but it’s clear now that the CDC should not be involved in any way with public health.

Thanks to the Freedom of Information Act (FOIA), we know that vaccines are not a miracle of modern medicine.  Any medical or government authority which insists vaccines prevent diseases is either ignorant of government documents (and endless studies) revealing the exact opposite or of the CDC’s attempts to hide the truth about vaccines from the public, or means harm to the public.

Thanks to the Freedom of Information Act (FOIA), we know the vaccine schedule is a hoax.
The health danger to American children and adults are vaccines.

“The greatest lie ever told is that vaccines are safe and effective”
-Dr. Len Horowitz

Source

http://www.endalldisease.com/the-vaccine-hoax-is-over-secret-documents-reveal-shocking-truth/

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Evidence emerges that seasonal flu vaccine increases risk of H1N1 swine flu. See:http://abundanthope.net/pages/Health_and_Nutrition_37/Evidence_emerges_that_seasonal_flu_vaccine_increas_3713.shtml

H1N1 Vaccine Patent Filed (2007) Long Before the Swine Flue Virus Was Spread! See:http://abundanthope.net/pages/True_US_History_108/H1N1_Vaccine_Patent_Filed_2007_Long_Before_the_Swi_3544.shtml

INOCULATIONS: THE TRUE WEAPONS OF MASS DESTRUCTION CAUSING VIDS (VACCINE INDUCED DISEASES) (AN EPIDEMIC OF GENOCIDE) See:http://abundanthope.net/pages/True_US_History_108/INOCULATIONS_THE_TRUE_WEAPONS_OF_MASS_DESTRUCTION__3264.shtml

Refusing vaccination labels you a “criminal”, so says WHO. See:http://abundanthope.net/pages/Political_Information_43/Refusing_vaccination_labels_you_a_criminal_so_says_3428.shtml

Aspirin kills 400% more people than H1N1 swine flu. See: http://abundanthope.net/pages/Health_and_Nutrition_37/Aspirin_kills_400_more_people_than_H1N1_swine_flu_4030.shtml

Len Horowitz files pandemic charges against Rockefeller. See: http://abundanthope.net/pages/True_US_History_108/Len_Horowitz_files_pandemic_charges_against_Rockef_3684.shtml

Toddlers will have jabs for SIX diseases at once. See: http://abundanthope.net/pages/Health_and_Nutrition_37/Toddlers-will-have-jabs-for-SIX-diseases-at-once.shtml

78 percent of Pakistani children with polio were given polio vaccines. See: http://abundanthope.net/pages/Health_and_Nutrition_37/78-percent-of-Pakistani-children-with-polio-were-given-polio-vaccines.shtml

Vaccine-Induced Disease Epidemic Outbreaks. See:http://abundanthope.net/pages/Health_and_Nutrition_37/Vaccine-Induced_Disease_Epidemic_Outbreaks_3555.shtml

PJ #48 ” TANGLED WEBS VOL. V “, chapter 9 & 10.See: http://abundanthope.net/pages/Phoenix_Journals_61/PJ-48-TANGLED-WEBS-VOL-V-chapter-9-10.shtml

How to Fabricate a “Deadly Pandemic” Out of Thin Air! See:http://abundanthope.net/pages/Political_Information_43/How_to_Fabricate_a_Deadly_Pandemic_Out_of_Thin_Air_3171.shtml

A Blast From the Past: Swine Flu Redux. See: http://abundanthope.net/pages/True_US_History_108/A_Blast_From_the_Past_Swine_Flu_Redux_3170.shtml

The Caduceus Decoded: Secret Symbols Reveal Dark Agenda of Western Medicine. See:http://abundanthope.net/pages/Health_and_Nutrition_37/The_Caduceus_Decoded_Secret_Symbols_Reveal_Dark_Ag_3249.shtml

PJ #8 AIDS, Last Great Plague Chapters 6 & 7. See: http://abundanthope.net/pages/Phoenix_Journals_61/PJ_8_AIDS_Last_Great_Plague_Chapters_6_amp_7_2921.shtml

PJ #8 AIDS, the Last Great Plague Intro and Chapter 1. See: http://abundanthope.net/pages/Phoenix_Journals_61/PJ_8_AIDS_the_Last_Great_Plague_Intro_and_Chapter__2918.shtml

Interview with Dr Lorraine Day on Vaccines, anti-biotics and the North American Union. See:http://abundanthope.net/pages/True_US_History_108/Interview_with_Dr_Lorraine_Day_on_Vaccines_anti-bi_2887.shtml

‘Accidental’ Contamination Of Vaccine With Live Avian Flu Virus Virtually Impossible. See:http://abundanthope.net/pages/True_US_History_108/Accidental_Contamination_Of_Vaccine_With_Live_Avia_2854.shtml

Universal Vaccine for the Flu? Look No Further Than Vitamin C and Zinc. See:http://abundanthope.net/pages/Health_and_Nutrition_37/Universal_Vaccine_for_the_Flu_Look_No_Further_Than_2715.shtml

The new eugenics: Life in our vast chemical vats. See: http://abundanthope.net/pages/Health_and_Nutrition_37/The-new-eugenics-Life-in-our-vast-chemical-vats.shtml

Vaccines-found-to-activate-moron-genes-that-cause-further-belief-in-vaccines-satire. See: http://abundanthope.net/pages/Health_and_Nutrition_37/Vaccines-found-to-activate-moron-genes-that-cause-further-belief-in-vaccines-satire.shtml

Vaccines for Deadly Malaria Create Even More Virulent Malaria: PLoS Study. see: http://abundanthope.net/pages/Health_and_Nutrition_37/Vaccines-for-Deadly-Malaria-Create-Even-More-Virulent-Malaria-PLoS-Study.shtml

CDC Pushes Flu Vaccine for Children in New Fear-Mongering Campaign. See: http://abundanthope.net/pages/Health_and_Nutrition_37/CDC-Pushes-Flu-Vaccine-for-Children-in-New-Fear-Mongering-Campaign.shtml

Hundreds of children at risk after bungling doctor gives incorrect vaccines. See: http://abundanthope.net/pages/Health_and_Nutrition_37/Hundreds-of-children-at-risk-after-bungling-doctor-gives-incorrect-vaccines.shtml

naturalnews.com printable article

Originally published March 2 2011

Dr. Jonas Salk, inventor of polio vaccine, exposed as criminal-minded scientist who conducted illicit medical experiments on mental patients

by Mike Adams, the Health Ranger, NaturalNews Editor

(NaturalNews) Dr. Jonas Salk, one of the “gods” in the cult of pharmacology — a man who is credited with inventing the polio vaccine – has now been exposed as a medical criminal who conducted illegal medical experiments on mental patients. This fact has come to light courtesy of the Associated Press, believe it or not, which has been investigating the history of medical experiments as part of a press effort leading up to scheduledbioethics meetings in Washington.

According to the Associated Press, Dr. Jonas Salk co-authored a clinical trial that “injected experimental flu vaccine in male patients at a state insane asylum in Ypsilanti, Mich., then exposed them to flu several months later.” The victims of this medical experiment were described as “senile and debilitated,” meaning that obtaining their rational consent to participate in such experiments would have been impossible. And that means Dr. Jonas Salk — one of the most highly-worshipped figures throughout modern medicine — was conducting this trial in violation of medical ethicsand in violation of the law.

Isn’t it interesting how the vaccine industry and its medical journal propaganda mouthpieces always hurl accusations at people like Dr. Andrew Wakefield, claiming he violated medical ethics for taking blood samples with consent, but when one of their own heroes gets caught engaging incriminal medical experiments involving the injection of insane mental patients without consent, they have nothing to say about it?

In the pro-vaccine cult of pharmacology, any researcher who concludes that vaccines are good for you is considered “right” no matter what laws they violate, what victims they kill or what kind of evils they have to commit in order to achieve their fabricated results. The vaccine industry, as we see throughout history, has openly allowed criminal scientists to operate its clinical trials — even when human victims were maimed or killed in the process. (And not much has changed since, it seems…)

 

The Big Lie about the polio vaccine

This trial involving Dr. Jonas Salk was, not surprisingly, federally funded. And it’s just the beginning of the lies and deceptions about Dr Jonas Salkand the polio vaccine. For starters, the polio vaccine was a failure and didn’t eradicate polio at all, but we’ll save that discussion for another story. Today’s topic is illegal medical experiments conducted by mad scientists working for the vaccine and pharmaceutical industries.

And on that topic, the true history of the criminal medical experiments that have been done in order to boost the profits of Big Pharma will absolutely shock you. As the AP reports:

“The late 1940s and 1950s saw huge growth in the U.S. pharmaceutical and health care industries, accompanied by a boom in prisoner experiments funded by both the government and corporations. By the 1960s, at least half the states allowed prisoners to be used as medicalguinea pigs.”

This is the result of Big Pharma leaning on state authorities, of course. Where profits are to be made, human rights have never gotten in the way. In fact, as the historical record clearly shows, the U.S. government has repeatedly conspired with the drug industry to use innocent human beings as unwitting guinea pigs in dangerous, deadly medical experiments.

The history of vaccines, you see, is a history filled with criminal misconduct on the part of medical researchers such as Dr. Jonas Salk (and many others). These were not heroes of science; they were pharma-funded criminal minds who routinely violated the foundations of medical ethics in order to trick prisoners, mental patients and the elderly into serving as their medical guinea pigs.

 

The criminal history of vaccines

Vaccines are founded on a history of deception and criminality, and now even the Associated Press has realized it, too.

AP reports that in 1963, for example, “Researchers injected cancer cells into 19 old and debilitated patients at a Jewish Chronic Disease Hospital in the New York borough of Brooklyn to see if their bodies would reject them.” This was a pharma-funded experiment, of course, conducted by yet another criminal-minded researcher claiming to be carrying out “science.”

That’s the other angle in all this, of course: All these criminal, inhumane medical experiments were carried out in the name of “science.”Whether they were infecting blacks, injecting prisoners, or hiring prostitutes to spread sexually-transmitted disease (another true experiment funded in part by the NIH), all these criminal activities were carried out under the label of “science.”

The AP goes on to report:

“In widely covered congressional hearings in 1973, pharmaceutical industry officials acknowledged they were using prisoners for testing because they were cheaper than chimpanzees.”

Yes! Cheaper than chimpanzees! Gotta love Big Pharma for their cost-saving efforts, eh? This is yet another example of the mindset of Big Pharma and “scientific” researchers who put humans lower than animals on the value scale.

 

Now Big Pharma is conducting medical experiments on victims in developing nations

Several of the worst medical experiments yet known are described in great detail by the AP report, including this one:

“Holmesburg Prison in Philadelphia made extensive use of inmates for medical experiments. Some of the victims are still around to talk about it. Edward ‘Yusef’ Anthony, featured in a book about the studies, says he agreed to have a layer of skin peeled off his back, which was coated with searing chemicals to test a drug. He did that for money to buy cigarettes in prison.”

“I said ‘Oh my God, my back is on fire! Take this … off me!’” Anthony said in an interview with The Associated Press, as he recalled the beginning of weeks of intense itching and agonizing pain. (http://www.aolnews.com/2011/02/27/horrific-us-medical-experiments-com…)

Of course, as many of these gross criminal activities came to light, the U.S. government was finally forced to put a stop to it due to public outcry. So the drug companies simply moved their criminal operations offshore where they now engage in routine medical experimentation on children in developing nations, usually by paying off top government officials in those countries to look the other way while their scientists and researchers unleash “pharma crimes” upon the people there.

This is how the experiments in Guatemala came about (http://www.naturalnews.com/029924_medical_experiments_Guatemala.html).

 

The long but true history of Big Pharma’s medical experiments in the name of “science”

NaturalNews, of course, began reporting on these medical experiments in 2006 when we featured a timeline of human medical experimentation in the United States (http://www.naturalnews.com/019189.html).

Here’s part two of that timeline: http://www.naturalnews.com/019187.html

In the last five years, the mainstream media was all but silent on this issue, failing to report much of anything on the pharma / government medical experimentation conspiracy until the Guatemala experiments were thrust onto the national spotlight in 2010. At that time, most people who learned about the criminal medical experiments carried out by the NIH and funded by the U.S. government were absolutely shocked… even stunned by the idea that this could have been done by the pharmaceutical industry or their own government.

And yet the Guatemala incident barely scratches the surface of what has really gone on behind the scenes, under the name of “science” and through the “conspiracy of profit” that has been operated by Big Pharma and the U.S. government for generations.

Dr. Jonas Salk was part of that criminal conspiracy, of course. Not only is he now implicated in these criminal medical experiments, but as you will see here on NaturalNews in upcoming articles, the credit given to Dr. Salk for ending polio is based on a fraudulent misrepresentation of the historical data – something that was intentionally done by the vaccine industry in order to convince people that vaccines ended polio!

The truth is far different. The “success” of the polio vaccine has been a 60-year lie. A the “heroic” stature of Dr. Jonas Salk has been a 70-year lie. This man was a Big Pharma criminal. And the truth about him — and his deadly vaccines — is finally coming out.

Watch for more reporting here on NaturalNews that exposes the 60-year lie about the polio vaccine and the supposed “heroes of medicine” who were actually criminal-minded scientists working for the drug companies and exploiting human lives to test their deadly chemicals and vaccines.

The truth about the history of Big Pharma and vaccines is finally coming out, folks. And they can’t claim it’s just a bunch of “conspiracy theories” anymore: This information is now being published in the mainstream media. And there’s a lot more to come.

Sources for this story include:
http://www.aolnews.com/2011/02/27/horrific-us-medical-experiments-com…

http://www.washingtonpost.com/wp-dyn/content/article/2011/02/27/AR201…

http://news.yahoo.com/s/ac/20110302/us_ac/7959022_us_government_medic…

 

Read Full Post »

assalaamu alaykum .

Below is an shocking article of false propagation in Pakistan regarding the anti polio vaccine ingredients,

Pakistan’s media and governments are well controlling the let out of truthful information regarding the death, injury and ingredients of polio vaccines.

The statements in this ridiculous article are a absolute blatant lie!

Any look at just any leaflet of a anti polio vaccine will show all the haraam and anti Islamic ingredients.

The public has to made aware of the sickening and toxic and haraam ingredients.

please look at the end of the article whereby i posted the ingredients of polio vaccines and its side effects.

wa salaam

No anti-Islam ingredients in polio vaccine, says top cleric

* CDGL launches campaign in city with focus on Afghans

Staff Report

LAHORE: There are no anti-Islam or anti-religion ingredients in the polio vaccine being used to eradicate the disease, a top religious scholar said on Saturday. Maulana Abdul Khabir Azad also took part in the inaugural session of a fresh campaign launched by the City District Government Lahore, which targets the city’s thickly populated areas inhabited by the Afghans.

Earlier in the day, the CDGL launched its three-day polio vaccination campaign from the Delhi Gate’s Shahi Hamam area. District Coordination Officer Noorul Amin Mengal, CM’s Health Adviser Khwaja Salman Rafiq, Islamic scholar Maulana Abdul Khabir Azad, EDO Health, EDO Education and other concerned officers were present on the occasion.

Addressing the ceremony, the DCO said that parents should administer polio drops to their children below five years age so that the new generation could be saved from this fatal disease. He said that it was the responsibility of parents to administer polio drops to their children for their save future. Mengal stated the CDGL was utilising all resources for eradication of polio from the Pakhtoon, Baloch and Afgan residential areas in the city. Advisor to CM Khwaja Salman Rafiq said that Punjab Government is trying to eradicate polio from Punjab and we shall eradicate this fatal disease.

http://www.dailytimes.com.pk/default.asp?page=2012%5C12%5C16%5Cstory_16-12-2012_pg13_6

Vaccine Ingredients – A Shocking List!

Vaccine Ingredients
Below is a list of ingredients in vaccines. (It is not exhaustive – there are other chemicals not in the list.)
If you are tempted to assume that these poisons would only be in harmless quantities in vaccines, note:
1) There is no safe level for some of these poisons, such as formaldehyde and mercury, even if one of them was consumed or injected on its own.
2) Even if the quantity of any given ingredient was within a safe level, remember that a large number of these are being taken in all at once, which can lead to the accumulative toxicity being much higher.
3) Poisons such as formaldehyde and mercury are well known to have a sensitising effect on the body, i.e. they cause increased susceptibility to any foreign substance that it might encounter at the same time or in the future.
4) Even the manufacturers admit to a large list of adverse effects of vaccines, including even death.
The resultant damage, including brain damage, from these toxins can vary from mild enough not to be apparent, through to severe, in some cases death. You cannot inject a living being with these poisons and expect there to be no adverse effect at all. What varies, and varies greatly, is merely the degree of damage. The reason for the large variation in this degree of damage include:
  • great genetic variations in recipients, affecting susceptibility in general and susceptibility to specific vaccines
  • variations within one recipient from one time to another (due to biorhythms, other work the immune system is doing already fighting other infections, how many vaccines have already been given, etc), and
  • variations between vaccine batches – there is an acknowledged weakness in the area of controlling the levels of toxins in vaccines, resulting in some batches being labelled “hot lots”. (Sadly even this identification does not necessarily result in recalls, but rather in distributing the “hot lot” as broadly as possible, as revealed in a leaked letter from a pharmaceutical company.)
Post mortems on cot death babies indicate asphyxia, which can be due to the level of poisons being just that little bit too high for these individuals’ immature immune systems to mount a defence of the strength and sustained period of time required to deal with them. Adding to the difficulty in dealing with the large load of poisons is the fact that these poisons interfere with the activities of the immune system itself, and thus weaken its ability to eliminate any poisons. In the younger babies the battle is more often lost within hours or a few days from the injection. In the older babies they more often hold out longer and only lose the battle after a few weeks or longer (J Pediatrics 1982).
For chemical profiles and definitions, visit http://www.scorecard.org/.
Sources: EDF (Environmental Defense Fund) & MME (Mosby’s Medical Encyclopaedia)
Formaldehyde:
(Used in vaccines as a tissue fixative)
Aust. National Research Council: Fewer than 20% but perhaps more than 10% of the general population may be susceptible to formaldehyde and may react acutely at any exposure level. More hazardous than most chemicals in 5 out of 12 ranking systems, on at least 8 federal regulatory lists, ranked as one of the most hazardous compounds (worst 10%) to ecosystems and human health (Environmental Defense Fund).
It is not safe at ANY level.
National Academy of Science:
There is no population threshold for irritation effects.
National Research Council:
Fewer than 20% but perhaps more than 10% of the general population may be susceptible to formaldehyde and may react acutely at any exposure level.
Formaldehyde is oxidised to formic acid which leads to acidosis and nerve damage. Acidosis can be described as a condition in which the acidity of the body tissues and fluids is abnormally high. The liver and the kidneys may also be damaged.
Other effects:
Eye; nasal; throat and pulmonary irritation; acute sense of smell; alters tissue proteins; anaemia; antibodies formation; apathy; blindness; blood in urine; blurred vision; body aches; bronchial spasms; bronchitis; burns nasal and throat; cardiac impairment; palpitations and arrhythmias; central nervous system depression; changes in higher cognitive functions; chemical sensitivity; chest pains and tightness; chronic vaginitis; colds; coma; conjunctivitis; constipation; convulsions; corneal erosion; cough; death; destruction of red blood cells; depression; dermatitis; diarrhoea; difficulty concentrating; disorientation; dizziness; ear aches; eczema; emotional upsets; ethmoid polyps; fatigue; fecula bleeding; foetal asphyxiation (and they don’t know what could cause SIDS?); flu-like or cold like illness; frequent urination with pain; gastritis; gastrointestinal inflammation; headaches; haemolytic anaemia; haemolytic haematuria; hoarseness; hyperactive airway disease; hyperactivity; hypomenstrual syndrome; immune system sensitiser; impaired (short) attention span; impaired capacity to attain attention; inability or difficulty swallowing; inability to recall words and names; inconsistent IQ profiles; inflammatory diseases of the reproductive organs; intestinal pain; intrinsic asthma; irritability; jaundice; joint pain; aches and swelling; kidney pain; laryngeal spasm; loss of memory; loss of sense of smell; loss of taste; malaise; menstrual and testicular pain; menstrual irregularities; metallic taste; muscle spasms and cramps; nasal congestions; crusting and mucosae inflammation; nausea; nosebleeds; numbness and tingling of the forearms and finger tips; pale, clammy skin; partial laryngeal paralysis; pneumonia; post nasal drip; pulmonary oedema; reduced body temperature; retarded speech pattern; ringing or tingling in the ear; schizophrenic-type symptoms; sensitivity to sound; shock; short term memory loss; shortness of breath; skin lesions; sneezing; sore throat; spacey feeling; speaking difficulty; sterility; swollen glands; tearing; thirst; tracheitis; tracheobronchitis; vertigo; vomiting blood; vomiting; wheezing.
References; C. Wilson; Chronic Exposure and Human Health (1993), McFarland & Company taken from Our Toxic Times Feb 1997 pgs 18 & 19.
Mercury:
(Used in vaccines as a preservative.)
Before you say, “But haven’t they removed mercury from the vaccines on the childhood vaccination schedule?” read this:Vaccines Are Not Mercury Free
See this video filmed by the University of Calgary of an actual brain neuron – watch what happens to it when it is exposed to (a low amount of) mercury: http://commons.ucalgary.ca/mercury/ The following is a written article about this video:http://unisci.com/stories/20011/0327013.htm
Mercury is the second most poisonous element known to man (next to uranium and its derivatives). As illustrated in the above video, neurons are observed to disintegrate in its presence. It has also been found to cause changes to chromosomes.
The U.S. has known about the potential problems of thimerosal (compound in vaccines that contains mercury) for many years. The World Health Organization voiced concerns as far back as 1990. Mercury is a highly toxic element which does not easily leave the body. Once ingested, injected, or inhaled, it stays and accumulates. An infant can receive in one day’s doses of vaccines as much as the absolute maximum set by the W.H.O. for 3 months of exposure, but it is not safe at ANY level.
Thimerosal is listed as a recognized developmental toxicant as well as a suspected skin or sense organ toxicant by the Environmental Defense Fund1. The following was taken from a website affiliated with the National Institutes for Health2:
“Symptoms of exposure to this class of compounds includes aphthous, stomatitis, catarrhal gingivitis, nausea, liquid stools, pain, liver disorder, injury to the cardiovascular system and hematopoietic system, deafness and ataxia. Exposure may be fatal. Headache, paresthesia of the tongue, lips, fingers and toes, other non-specific dysfunctions, metallic taste, slight gastrointestinal disturbances, excessive flatus and diarrhea may occur. Acute poisoning may cause gastrointestinal irritation and renal failure. Early signs of severe poisoning include fine tremors of extended hands, loss of side vision, slight loss of coordination in the eyes, speech, writing and gait, inability to stand or carry out voluntary movements, occasional muscle atrophy and flexure contractures, generalized myoclonic movements, difficulty understanding ordinary speech, irritability and bad temper progressing to mania, stupor, coma, mental retardation in children, skin irritation, blisters and dermatitis. Other symptoms include chorea, athetosis, tremors, convulsions, pain and numbness in the extremities, nephritis, salivation, loosening of the teeth, blue line on the gums, anxiety, mental depression, insomnia, hallucinations and central nervous system effects. Exposure may also cause irritation of the eyes, mucous membranes and upper respiratory tract.”
References:
1.) Environmental Defense Fund - http://www.scorecard.com/
2.) National Institutes for Health -
http://ntp-db.niehs.nih.gov/NTP_Reports/NTP_Chem_H&S/NTP_Chem5/Radian54-64-8.txt
Here is an excerpt from “The Vaccine Guide: Making an Informed Choice” (Randall Neustaedter, North Atlantic Books, 1996):
“Sensitivities to thimerosal in vaccines apparently develop as a result of previous vaccinations (Förström et al., 1980). Even the minute amount of thimerosal used in vaccines (.1 to .01%) can specifically stimulate the immune system and cause sensitization (Aberer, 1991). Mercury is a violent poison with many toxic effects. The toxicity of mercury varies depending on the form in which the element appears. Metallic mercury has different effects than inorganic or organic mercury compounds. However, major differences in toxicity are not expected among the different compounds within the inorganic group of mercury salts (Clement, 1992)…
…The neurologic toxicity symptoms caused by mercury compounds have a delayed onset after exposure (Bakir et al, 1973), which may have significance for the suspected long-term neurologic symptoms of learning disabilities and behaviour disorders associated with vaccines. (For full references, refer to book.)”
Antifreeze:
(This is in the polio vaccine.) Classed as “Very Toxic Material”. May lead to kidney, liver, blood and central nervous system (CNS) disorders. Harmful or fatal if swallowed. Effects include behavioural disorders, drowsiness, vomiting, diarrhoea, visual disturbances, thirst, convulsions, cyanosis, and rapid heart rate, CNS stimulation, depression, cardiopulmonary effects, kidney disorders. May also lead to liver and blood disorders. Produces reproductive and developmental effects in experimental animals.
Aluminium:
EDF Suspected – cardiovascular or blood toxicant, neurotoxicant, respiratory toxicant. Implicated as a cause of brain damage; suspected factor in Alzheimer’s Disease, dementia, convulsions and comas. More hazardous than most chemicals in 2 out of 6 ranking systems. On at least 2 federal regulatory lists. (This element is not toxic when only in trace amounts, indeed at such levels is even beneficial to the body, however a trace amount is extremely minute – the level in vaccines is enormously higher, at around 0.5%)
2-Phenoxyethanol:
EDF Suspected – developmental toxicant, reproductive toxicant. Metabolic poison (i.e. interferes with the metabolism in all cells). Capable of disabling the immune system’s primary response. Contains phenol (see below).
Phenol:
EDF Suspected – cardiovascular or blood toxicant aka Carbolic Acid, developmental toxicant, gastrointestinal or liver toxicant, kidney toxicant, neurotoxicant, respiratory toxicant, skin or sense organ toxicant. More hazardous than most chemicals in 3 out of 10 ranking systems. On at least 8 federal regulatory lists
Methanol:
Described as a volatile, flammable and poisonous liquid alcohol. In industry, it is used as a solvent and an antifreeze compound in fuel. In the body it is metabolised to formaldehyde (see above). Whilst it can be found naturally in the pectin that is present in some common fruits, it is only in very small quantities in fruit and does not pose a danger to the body in that form.
Borax
(sodium tetraborate decahydrate):
Traditionally used as a pesticide, including ant killer. Suspected cardiovascular or blood toxicant, endocrine toxicant, gastrointestinal or liver toxicant and neurological toxicant. Found to cause reproductive damage and reduced fertility in a study on rats.
Glutaraldehyde:
Poisonous if ingested (would be worse if injected). Causes birth defects in experimental animals.
MSG
(monosodium glutamate):
In a 1995 report by the Federation of American Societies for Experimental Biology (FASEB) two groups of people were defined as intolerant of MSG – those who eat large quantities of MSG (which is in many processed foods as a flavour enhancer – # 621) and those with “severe, poorly controlled asthma”. (Can you guess now why sensitivity to MSG is so common?) According to this report which was contracted by the FDA the following are symptoms that they found in reaction to MSG.
A. Burning sensation in the back of the neck, forearms and chest
B. Numbness in the back of the neck, radiating to the arms and back
C. Tingling, warmth, and weakness in the face, temples, upper back, neck and arms
D. Facial pressure or tightness
E. Chest pain
F. Headache
G. Nausea
I. Rapid heartbeat
J. Bronchospasm (difficulty breathing) in MSG-intolerant people with asthma
K. Drowsiness
L. Weakness
An FDA web page called “FDA and Monosodium Glutamate (MSG)” states “Injections of glutamate in laboratory animals have resulted in damage to nerve cells in the brain.”
In 1978 MSG was removed from baby food and other baby products for infants less than one year of age because the American Academy of Pediatrics and the National Academy of Sciences expressed concerns.
Sulfate and phosphate compounds
(to one or more of which your child may have already developed a severe allergy from past vaccinations.)
Ammonium Sulfate:
EDF Suspected – gastrointestinal or liver toxicant, neurotoxicant, respiratory toxicant.
Gentamicin Sulfate:
an antibiotic.
Neomycin Sulfate:
an antibiotic. Interferes with Vitamin B6 absorption. An error in the uptake of B6 can cause a rare form of epilepsy and mental retardation.
Tri(n)butylphosphate:
EDF Suspected – kidney toxicant, neurotoxicant. More hazardous than most chemicals in 2 out of 3 ranking systems. On at least 1 federal regulatory list.
Polymyxin B:
another antibiotic
Polysorbate 20 / 80:
EDF Suspected – skin or sense organ toxicant. Known to cause cancer in animals.
Sorbitol:
EDF Suspected – gastrointestinal or liver toxicant. Less hazardous than most chemicals in 1 ranking system.
Polyribosylribitol:
a component of the Hib bacterium.
Beta-Propiolactone:
EDF Recognized – carcinogen, EDF Suspected – gastrointestinal or liver toxicant, respiratory toxicant, skin or sense organ toxicant. More hazardous than most chemicals in 3 out of 3 ranking systems. On at least 5 federal regulatory lists. Ranked as one of the most hazardous compounds (worst 10%) to humans.
Amphotericin B:
MME definition – “a drug used to treat fungus infections. Known allergy to this drug prohibits use. Side effects include blood clots, blood defects, kidney problems, nausea and fever. When used on the skin, allergic reactions can occur.”
Animal organ tissueand blood:
Animal cell lines need to be used to culture the viruses in vaccines, so this material is included in the formulation that is injected. Other than when this protein material is digested (i.e. consumed and broken down into its component amino acids, etc, before absorption), it is unusable and toxic to the body. It can also contain many animal viruses (see Animal Viruses).
Animals used include monkey (kidney), cow (heart), calf (serum), chicken (embryo and egg), duck (egg), pig (blood), sheep (blood), dog (kidney), horse (blood), rabbit (brain), guinea pig, etc.
Aborted human foetal tissue and human albumin:
This is something you might like to consider if you are against abortion. Also from a health point of view tissue from another human (not just animals) is still foreign and therefore toxic to the body.
Large foreign proteins:
In addition to the above accompanying (protein) material, there are large proteins that are deliberately included, used for such purposes as adjuvants (i.e. to help get an immune “response”). Egg album and gelatin (or gelatine, obtained from selected pieces of calf and cattle skins, de-mineralized cattle bones and pork skin) are in several vaccines. Casein (milk protein) is in the triple antigen, i.e. DPT vaccine. As explained above, when injected, proteins are toxic to the body. Hence the immune system “response” – it is stressed by this invasion, which results in sensitisation – it becomes sensitive to these substances, not immune to them.
Is it any wonder, then, that allergies to these substances are now so common (in the case of milk, resulting in the relatively recent emergence of milk alternatives such as soy and rice “milk”s)?
Latex:
This is in the hepatitis B vaccine which is given routinely to health workers. Have you heard about the problem of the high occurrence of latex allergy among nurses? How do you think they became sensitised to latex? Allergic reactions can be life-threatening. Hepatitis B vaccine is now routinely given to newborn babies in many countries, including Australia and the US.
Animal Viruses:
Some of these can be particularly alien to the human body. The most frequently documented and publicised example is the monkey virus SV40. This is harmless in monkeys, but inject it into a human and it can cause cancer – in the brain (tumours), bone (e.g. multiple myeloma), lungs (mesothelioma) and lymphoid tissue (lymphoma). It has appeared in people born in the last 20 years (The Journal of Infectious Diseases, Sep 1999;180:884-887), long after the manufacturer claimed to have “cleaned up” the polio vaccine in which it was found. Such cases include the late Alexander Horwin, both of whose parents tested negative for SV40, therefore recent cases cannot just be blamed on inheritance from parents who received the vaccine (see www.ouralexander.org).
Human Viruses:
The viruses against which the vaccine is supposed to protect are frequently said to be “killed”, “inactivated” or “attenuated”. This is a myth. The main method used to inactivate viruses is treatment with formaldehyde, whose effectiveness is only limited, and even then only temporary – once the brew is injected into the body and disperses, it is documented in orthodox medical literature that these “killed” viruses can revert to their former virulence.(References for this are available.)
Please note also that whilst the included viruses, bacteria etc against which the vaccine is supposed to protect are claimed to be in “very small doses”, the  quantities are quite high enough for the diseases to occur, as they can do quite severely, occasionally even leading to death (e.g. deaths reported recently in the Lancet from yellow fever contracted from that vaccine). Indeed a susceptible person can succumb to infection when exposed to only a minute dose (particularly when directly injected), while a sufficiently healthy person will not succumb even when exposed, naturally that is, to an enormous dose. It is not the pathogen, but the interaction between pathogen and host that causes disease to appear (Intervirology 1993).
If the symptoms of a disease do not occur after a vaccine, it cannot be assumed that the person is not or will not be harmed by that pathogen. Most disease symptoms are actually the visible signs of the body’s effort to defend itself against the pathogen, and with injections, important defences are bypassed.
Bacteria and the toxins they produce:
The human blood is supposed to be, and traditionally was, sterile – no bacteria (or other organisms) present in it. That is not the case any more. Naturally this has a weakening effect on the immune system, apart from sometimes leading to severe bacterial infections.
Mycoplasma:
These are microscopic organisms lacking rigid cell walls and considered to be the smallest free-living organisms. Many are pathogenic and one species is a cause of mycoplasma pneumonia which interestingly is noted to occur “in children and young adults” (Mosby’s Medical Dictionary). So, are these only in vaccines by mistake as contaminants? No, believe it or not, they aredeliberately included as adjuvants, i.e. to increase the immune system’s “response” to the vaccine.
Genetically modified yeast:
This is in the hepatitis B vaccine. Given the controversy over the ingestion of genetically modified foods, how much less safe, do you think, is theinjection of them, particularly considering what follows below?
Foreign DNA:
This DNA is from such organisms as various animals, animal/human viruses, fungi and bacteria. It has been documented that the injecting foreign DNA can cause it or some of it to be incorporated into the recipient’s DNA (see‘Immunisation’ Against Diseases for Children). Remember, nature has not experienced such a direct invasion as this before, so can you be sure that it would have developed a way to protect your body against it?

 

Animal Ingredients in Vaccines
Should you vaccinate or shouldn’t you??
This is a topic that is much debated, especially by those who are Pro-Life and/or Vegan, as there is so much to consider when determining whether to immunize your child or not. I myself was astounded when I discovered the many dangerous and unethical ingredients in vaccines. Most of the ingredients in vaccines are extremely hazardous and toxic to our bodies, even in small quantities. Many contain live viruses! Trace amounts of the mediums in which vaccines are cultured can be found in them as well, such as chicken eggs, monkey kidney cells and aborted human fetal tissue (yes, can you believe this?!).Other ingredients include Ammonium Sulfate, Formalin (30% formaldehyde), Aluminum, Thimerosal (50% Mercury), Phenoxyethanol (Antifreeze).

Common ingredients in vaccines are animal byproducts, such as gelatin (a known allergen), serums, guinea pig embryo cells, or residual proteins, chicken embryo and embryonic fluid and human diploid cells from aborted fetal tissue, antibiotics such as Polymixin, Neomycin, Neomycin Sulfate, Gentamicin sulfate, Amphotericin B and Streptomycin.

With every child and adult on the planet a potential recipient of vaccines administered periodically throughout their lives, and every healthcare system and government being a potential buyer, it is little wonder that countless millions of dollars are being spent nurturing the growing multi-billion dollar vaccine industry.

Some experts have the opinion that the dangers of childhood diseases are greatly exaggerated in order to scare parents into compliance with a questionable but highly profitable vaccinations. In their opinion, the government and its mandatory regulations, are under the thumb of a traditional medical system grown fat on extreme drug profits.

Legal Exemptions to Vaccinations: Medical, Religious, and Philosophical exemptions are worded differently for each state. To use an exemption for your child, you must know specifically what the law says in your state.

  • Medical Exemptions: Medical Exemptions: All 50 states allow medical exemption to vaccination. Proof of medical exemption must take the form of a signed statement by a Medical Doctor (M.D.) or a Doctor of Osteopathy (D.O.) that the administering of one or more vaccines would be detrimental to the health of an individual. Most doctors follow the CDC and AAP guidelines. Some states will accept a private physician’s written exemption without question. Other states allow the state health department to review the doctor’s exemption and revoke it if health department officials don’t think the exemption is justified.
  • Religious Exemptions: Religious Exemption: All states allow a religious exemption to vaccination except Arkansas, Mississippi and West Virginia. The religious exemption is intended for people who possess a sincere religious belief against vaccination to the extent that if the state forced vaccination, it would be an infringement on their right to exercise their religious beliefs.
  • Philosophical Exemption: The following 17 states allow exemption to vaccination based on philosophical beliefs: Arizona, California, Colorado, Idaho, Louisiana, Maine, Michigan, Minnesota, New Mexico, North Dakota, Ohio, Oklahoma, Rhode Island, Utah, Vermont, Washington and Wisconsin. In many of these states, in order to use the philosophical objection or personal conviction exemption, individuals must object to all vaccines, not just a particular vaccine.

Vaccines and Their Ingredients

    • Polio – DPT contains: DPT – Diptheria and Tetanus Toxoids and Pertussis Vaccine Adsorbed SmithKline Beecham Pharmeceuticals Produced using aluminum phosphate, formaldehyde, ammonium sulfate, washed sheep red blood cells, glycerol, sodium chloride, thimerosal medium: porcine (PIG) pancreatic hydrolsate of casein.
    • Acel-Immune DTaP Diptheria and Tetanus Toxoids Acellular Pertussis Vaccine adsorbed Lederle Laboratories Produced using formaldehyde, thimerosal, aluminum hydroxide, aluminum phosphate, polysorbate 80, gelatin.
    • Act HIB Heamophilus Influenzae Type B (HIB) Tetanus Toxoid Conjugate Connaught Laboratories Produced using ammonium sulfate, formalin, sucrose, thimerosal Medium: semi-synthetic.
    • Attenuvax Measles Virus Vaccine Live Merck & Co, Inc. Produced using neomycin, sorbitol, hydrolized gelatin Medium: chick embryo.
    • DPT Diptheria and Tetanus Toxoids and Pertussis Vaccine Adsorbed SmithKline Beecham Pharmeceuticals Produced using aluminum phosphate, formaldehyde, ammonium sulfate, washed sheep red blood cells, glycerol, sodium chloride, thimerosal. Medium: porcine (pig) pancreatic hydrolsate of casein.
    • Hepatitis B SmithKline Beecham Pharmaceuticals Produced using aluminum hydroxide, thimerosal. Medium: yeast
    • IPOL Inactivated Polio Vaccine Connought Laboratories Produced using 3 types of polio virus, formaldehyde, phenoxyethanol (antifreeze), neomycin, streptomycin, polymixin B. Medium: VERO cells, a continuous line of Monkey kidney cells.
    • MMR Measles Mumps Rubella Live Viruse Vaccine Merck & Co., Inc. Produced using sorbitol, neomycin, hydrolized gelatin. Mediums: M&M – chick embryo. Rubella – Human diploid cells (originating from human aborted fetal tissue).
    • Orimune Poliovirus Vaccine Live Oral Trivalent Lederle Laboratories Produced using 3 types of attenuated polioviruses, streptomycin, neomycin, calf serum, sorbitol. Meduim: monkey kidney cell culture,
    • Varivax Varicella Virus Vaccine Live (chicken pox Vaccine) Merck & Co., Inc. Produced using sucrose, phosphate, glutamate, proceessed gelatin medium: Human Diploid Cells (originating from human aborted fetal tissue).
    • Vaccines Grown In Aborted Fetal Cell Cultures

:

    • Chickenpox, VARIVAX: Merck
    • Hepatitis A, VAQTA: Merck
    • Polio (oral), Poliovac, Canada: Connaught
    • Polio, IMOVAX: Connaught
    • Rabies, Imovax: Pasteur Merieux
    • Rubella, MERUVAX: Merck
    • Vaccines With Live Virus

:

    • Chickenpox, VARIVAX: Merck
    • Measles, ATTENUVAX: Merck
    • Measles and Mumps, M-M-Vax: Merck
    • Measles, Mumps and Rubella, M-M-RII: Merck
    • Measles and Rubella, M-R-VaxII: Merck
    • Mumps, MUMPSVAX: Merck
    • Rubella, MERUVAX: Merck
    • Rubella and Mumps: BIAVAX
    • Vaccines – Genetically-Engineered

:

    • Hepatitis B: Merck
    • Hepatitis B: SmithKline Beecham
    • Lyme, LYMERIX: SmithKline Beecham
    • RSV, Synapis: MedIMMUNE (vaccine or preventive treatment)
    • Vaccines With Animal And Cattle Parts

:

    • Chickenpox, VARIVAX — fetal bovine serum: Merck
    • Diphtheria, Tetanus, accelular Pertusssis, Acel-Immune — beef heart infusion: Lederle
    • Infanrix — bovine extract: SmithKline Beecham
    • Flu, FLUSHIELD — chick embryos: Wyeth: Fluzone — chicken embryos: Connaught
    • Measles, ATTENUVAX — hydrolyzed gelatin: Merck
    • Measles, Mumps and Rubella, M-M-RII — hydrolyzed gelatin: Merck
    • Mumps, MuMPSVAX — hydrolyzed gelatin: Merck
    • Polio, IPOL — calf serum, monkey kidney cells: Pasteur Merieux
    • Polio (oral), ORIMUNE — kidney cells, calf serum: Lederle
    • Rub

ella, MERUVAX — hydrolyzed gelatin: Merck

    • Rubella and Mumps, BIAVAX — hydrolyzed gelatin: Merck
    • Vaccines Using Cattle Material – (blood, fetal calf serum, meat broth–from countries U.S. government states have a RISK OF MAD COW DISEASES.)

:

    • Anthrax: *BioPort DPT Certiva, Anthrax: *BioPort DPT Certiva, , diptheria, pertussis, tetanus: North American/Baxter International
    • DPT: Infanrix, diptheria, pertussis, tetanus: GlaxoSmithKline Beecham
    • Hep A: *Havrix, hepatitis A: GlaxoSmithKline Beecham
    • Hib *ActHIB, haemophilus influenza Type B: Aventis Pasteur
    • Hib: *OmniHIB: haemophilus influenza Type B: GlaxoSmithKline Beecham

,li>Pneumonia, *PNU-IMUNE 23: Lederle/American Home Products

  • Polio IPOL: Aventis Pasteur

(source: Illiniois Vaccine Awareness Coalition (IVAC)

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