Donald Trump Speaks Out on the Autism – Vaccine Link

 

PHARMA: You Are Fired!  Parents are Holding You Accountable for the Autism Epidemic until Proven Otherwise.

Donald Trump publicly links vaccines to autism

Natural News
by Leslie Carol Botha, Vice President of Public Relations, SANE Vax Inc.
April 6, 2012

 

In a stunning development for the ostracized, often criticized, vaccine safety awareness movement, cause celebre and business mogul, Donald Trump raised concern about vaccinations on Monday, April 2, the anniversary of the fifth annual World Autism Awareness Day. Trump ‘warned’ Fox News viewers he “strongly believes that Autism Spectrum Disorders (ASD) are linked to exposure to vaccines.”1

During the interview, the tycoon revealed that a series of casual observations led him to the conclusion that ‘”monster” vaccinations cause Autism. The remark was probably a bombshell for pro-vaccine advocates including doctors, pharmaceutical companies, the government – and oh yes, Bill Gates. They have all fervently denied that observation -long a tenet of ‘science-based research’ – has anything to do with a medical outcome.

Trump acknowledged that speaking out against vaccines and the vaccine schedule is very controversial. But then he went on to state: “…I couldn’t care less. I’ve seen people where they have a perfectly healthy child, and they go for the vaccinations and a month later the child is no longer healthy.”

Trump’s statement is a victory for parents who have long believed vaccines contributed to the neurological damage their children suffered post -vaccination. Although Trump is not against vaccines, he has spoken out before regarding his concerns about the increasing number of required immunizations in the childhood vaccination schedule.

Autism Rates Rise with Increase in Vaccination Schedule

The Center for Disease Control (CDC) just released a study based on 2008 data revealing Autism rates have risen to an all-time high. Health records for 8 year old children in 14 states were analyzed showing Autism now affects 1 in 88 children; and 1 in 54 boys in the U.S.2.

Between 1960 and 1980 – children were subjected to 24 and 25 doses of vaccines. As of 2010, infants and children are exposed to 70 vaccines in the same time period. To put this in perspective – a child born today will receive more vaccine doses by the time he is six months old than his mother did by the time she went to college. With the addition of vaccinations to the adult schedule; a person will receive close to 167 vaccine doses over their lifetime. It is interesting to note that Alzheimer’s rates are also increasing as more vaccines are administered to senior citizens. Subsequently vaccine manufacturers are now wallowing in a 27 billion dollar a year industry. At what cost to our children; at what financial loss to America’s families?

The CDC data even becomes more compelling when individual state demographic rates are examined. The number of children identified with ASDs ranged from 1 in 210 children in Alabama to 1 in 49 children in New Jersey and 1 in 47 children in Utah. On the other hand the state of Iowa is showing 1 in 718 children are at risk for ASDs.

Four states – four different environments – with wide variations in state-wide levels of environmental toxic exposure. If one only considered the theory of environmental pollution, New Jersey, in comparison to the other three states would be an obvious concern. But, what about Iowa? Toxic chemicals from pesticides have certainly affected the waterways. And yet, their children are the most protected from ASDs. Alabama and Utah on the other hand have high rates of vaccination compliance – very low environmental pollution – and their rates of autism are showing the greatest concern. 3.

ASDs Neurological Disorders Now Showing in the Adolescent Population

With the introduction of HPV vaccines, Gardasil and Cervarix into the adolescent vaccine schedule, symptoms eerily similar to ASDs are now emerging in the 9 to 26 year old male and female population.

SANE Vax has been following the VAERS data over the past 6 months and have been saddened to see the increase in the number of adverse injuries and deaths that have occurred post-vaccination.

It is more than apparent government health authorities, politicians, and the medical industry are going to continue whitewashing the sacred vaccine cash cow until medical consumers are faced with the largest scandal the world has ever witnessed.

Medical consumers can no longer trust the “First do no harm” platitude. The harm has been done. The United States is dealing with a full-fledged Autism epidemic and the global media is reporting it. We cannot stand idly by and watch the pandemic spread throughout the world. Medical consumers must hold those in charge of creating this man-made plague accountable for their actions before it’s too late.

Source:

1. Trump warns Fox News viewers: Autism caused by vaccines http://www.rawstory.com
2. CDC Press Release- http://www.cdc.gov/media/releases/2012/p0329_autism_disorder.html
3. Autism Rates per State Updated http://www.stellamarie.com

 

SaneVax writes open letter to medical journal editor protesting bogus Gardasil study

 

 

 

22 February 2012

Dr. Ulf de Faire
Editor-in-Chief
Journal of Internal Medicine
e-mail: edit.off@jim.se

Open Letter to Journal of Internal Medicine editor

Dear Dr. de Faire:

This letter is to request the Editor to commission an Editorial, a Letter to the Editor or a Consensus Report to be published in the Journal to balance the weight of the conclusion in a highly biased study article entitled “Surveillance of autoimmune conditions following routine use of quadrivalent human papillomavirus vaccine,” by Chao et al., published in the February, 2012 issue of the Journal of Internal Medicine. 1

The Chao safety surveillance study of HPV-4 in routine use among women in the United States of America and in the European Union Member States was constructed as a post-licensure commitment to the FDA, the European Medicines Agency and other regulatory authorities. The study conclusion incorrectly states “No autoimmune safety signal was found in women vaccinated with HPV-4.”1

Chao et al. inappropriately selected Members of the Kaiser Permanente Southern California, Pasadena, CA and Kaiser Permanente Northern California, Oakland, CA as the subjects for the surveillance to extrapolate the result to the entire populations in the USA and the EU where the residents are largely ethnically Caucasian.

It is well known that the ethnic populations in Oaklandand Pasadena, CA, USAare not representative of the USAor EU member states. For example, the census of Oakland, CA shows that non-Hispanic whites constitute only 25.9% of the residents in 2010.2

Chao and co-authors from Kaiser Permanente knew, or should have known, that the prevalence of lupus erythematosus (and other autoimmune disorders) varies in different ethnic populations in California and elsewhere, due to either varied genetic constitution or diverse environmental influences, as reported by Fessel from Kaiser Permanente Medical Center.3

“In the United States, the incidence of systemic lupus erythematosus (SLE) varies by location and ethnicity. Incidence rates among children younger than age 15 years have been reported to be 0.5-0.6 case per 100,000 persons. Prevalence rates of 4-250 cases per 100,000 persons have been reported, with greater prevalence in Native Americans, Asian Americans, Latin Americans, and African Americans. In one study of adults, the incidence of lupus in African American females was estimated at 1 in 500. African American children may represent up to 60% of patients younger than 20 years with lupus.”4

It is astonishing that the incidence of systemic lupus erythematosus cases among unvaccinated women in the Chao study, was estimated to be 10.3 per 100,000 (Table 3), about 20 times the national incidence rate.

The census report also shows that 28.4% of the residents in Oakland, CA, USA were foreign born.2 All new young female immigrants are required to receive Gardasil vaccination before they are allowed to enter into the US.5 Therefore, 28.4% of the “unvaccinated” women in the Chao study, who were immigrants, might in fact have been unknowingly vaccinated with the HPV-4 before they became members of the Kaiser Permanente Health Care. As a result, autoimmune cases occurring after receipt of HPV-4 might have contributed to the high background of autoimmune condition incidence in the “unvaccinated” group, as determined by the imputation method in the Chao study.

Compared with the Caucasians, lupus nephritis is known to be more common in SLE patients of Chinese origin. Whether this is related to genetic or environment factors remains speculative.6 If the Kaiser Permanente membership has a significant number of ethnic Chinese subscribers, some SLE patients whose first presenting symptoms were those of lupus nephritis after Gardasil injections, might not be diagnosed in the follow-up period of 180 days, as stipulated in the Chao study.

It is most disturbing to read:

The multiple imputation approach was not a standard method for estimating background incidence rates. Furthermore, only the reviewed vaccinated cases were used to inform the imputation for new-onset status amongst the unvaccinated potential cases.”

So Chao and coauthors knew that the multiple imputation approach is “not a standard method” and “compared oranges to apples” while conducting their statistical analyses, in order to show the outcome of “no autoimmune safety signal”. This type of behavior borders on scientific fraud.

Of the many possibly relevant autoimmune conditions, only a few cherry picked examples were investigated. The conclusion of the study: “No autoimmune safety signal was found in women vaccinated with HPV4” is therefore inappropriate and grossly misleading.

In the interest of public health and safety, it is the obligation of the Journal Editor to commission an Editorial to balance the conclusion of the Chao article which is now being used as material for Continued Medical Education for physicians.

Any of the following scientists/medical professionals could be approached to provide such a commissioned Editorial: Dr. Christopher Shaw, Dept. of Ophthalmology and Visual Sciences, University of British Columbia (cashawlab@gmail.com), Dr. Lucija Tomljenovic, Dept. of Ophthalmology and Visual Sciences, University of British Columbia (lucijat77@gmail.com), Dr. Toni Bark, Boston University, (where.tonibark@mac.com), Dr. Romain Gherardi, Institut Mondor de Recherche Biomédicale, Univeriste (France.romain.gherardi@hmn.aphp.fr).

Respectfully,

Norma Erickson, President SANE Vax Inc.

 

Signed on behalf of the Board of Directors, SANE Vax, Inc.:
Leslie Carol Botha, Vice President of Public Relations
Janny Stokvis, Vice President of Research
Rosemary Mathis, Vice President, Victim Support
Freda Birrell, Secretary
Linda Thompson, Treasurer

 

References

  1. Chao C, Klein NP, Velicer CM, Sy LS, Slezak JM, Takhar H, Ackerson B, Cheetham TC, Hansen J, Deosaransingh K, Emery M, Liaw KL, Jacobsen SJ. Surveillance of autoimmune conditions following routine use of quadrivalent human papillomavirus vaccine.  J Intern Med. 2012;271:193-203.
  2. http://quickfacts.census.gov/qfd/states/06/0653000.html
  3. Fessel WJ Epidemiology of systemic lupus erythematosus. Rheum Dis Clin North Am. 1988;14:15-23.
  4. http://emedicine.medscape.com/article/1008066-overview
  5. http://online.wsj.com/article/SB122282354408892791.html#articleTabs=article
  6. Mok CC, Lau CS. Lupus in Hong Kong Chinese. Lupus. 2003;12:717-22.

Clinical pathologist wants taxpayers to pay for HPV Gardasil vaccination, but discouraged HPV DNA testing

Natural News

February 22, 2012
By Norma Erickson, President of SANEVAX, INC.

On January 1, 2011, Dr. Philip Castle became the first Executive Director of the American Society of Clinical Pathology (ASCP) Institute. Dr. Philip E. Castle also served on a data safety and monitoring board for human papillomavirus vaccines for Merck and is well known for his proposals directing publicly financed programs or insurers to pay for vaccination of HPV-naive girls (ages 11-12) as a comprehensive strategy for cervical cancer prevention[1].

Now he is also known for accusing physicians of abusing HPV DNA testing in fairly large numbers[2].

But one gynecologist is firing back as Dr. Castle does not even have a license to practice medicine and has never handled a clinical problem facing a patient. Read her article herehttp://gynogab.blogspot.com.

It is incomprehensible to not test the HPV infections after mass vaccination of young girls. Is HPV DNA testing the way to find out if the vaccine really works?

How can a pathologist like Dr. Castle direct the activities of the American Society for Clinical Pathology Institute?

Are American clinical pathologists interested in medical science? Or are they only concerned with promoting HPV vaccines with publicly funded programs?

References

1.Castle PE, Zhao FH. Population effectiveness, not efficacy, should decide who gets vaccinated against human papillomavirus via publicly funded programs. J Infect Dis 2011; 204: 335-7.http://jid.oxfordjournals.org/content/204/3/335.full.pdf+html

2.Castle PE. Abuses in human papillomavirus DNA testing. Obstet Gynecol 2011;118:1-3.http://www.ncbi.nlm.nih.gov/pubmed/21691156

Read the entire article here.

Dr. Hanan Polansky on the Radio, Explains How Foreign DNA Fragments in Vaccines Can Cause Disease

Yahoo

PRWeb

Dr. Hanan Polansky from the CBCD, used his discovery of microcompetition to explain the biological mechanism underlying the serious adverse events of Gardasil.

Rochester, New York (PRWEB) February 14, 2012

In a recent radio interview, Dr. Hanan Polansky from the Center for the Biology of Chronic Disease (CBCD) used his discovery of microcompetition to explain the biological mechanism underlying the serious adverse events of Gardasil, the HPV vaccine. The broadcast also featured Norma Erickson, President of SANE Vax Inc. and was hosted by Leslie Carol Botha.

A recording of the interview is available on the CBCD website at http://www.cbcd.net.

Dr. Hanan Polansky discovered that foreign DNA fragments called N-boxes can cause disease. When these foreign DNA fragments enter the body (naturally, or artificially, like through an injection of a vaccine or other treatments), they end up in the cell’s nucleus, where they attract scarce genetic resources. The “microcompetition” between the foreign N-boxes and the human N-boxes cause the human genes to malfunction, which, in turn, can lead to disease.

Dr. Hanan Polansky’s discovery has important implications. It suggests that by stopping or preventing microcompetition we can cure and prevent major diseases, such as cancer, heart disease, diabetes, autoimmune diseases, and even obesity.

Dr. Hanan Polansky is the author of the highly acclaimed “Purple” book, entitled “Microcompetition with Foreign DNA and the Origin of Chronic Disease.” In his book he explains how foreign DNA fragments can cause many major diseases without damaging (mutating) the human DNA. The book has been read by more than 5,000 scientists around the world, and has been reviewed in more than 20 leading scientific journals.

Ramji L. Khandelwal, PhD – Professor, Department of Biochemistry, University of Saskatchewan, Canada, said on the book: “This is an excellent book that provides published data from a very different perspective to formulate a generalized theory in terms of stable good health … I am confident that this theory will be validated with future work. It has already provided stimulus to my thinking, and so far, I agree with the basic concepts outlined in this book.”

The CBCD encourages biologists, virologists, geneticists and scientists and the general public to obtain a copy of Dr. Hanan Polansky’s book and read it. The book is available as a free download from the CBCD website.

The CBCD endorses Dr. Polansky’s theory, and invites the media, scientists, and the general public to contact us on this issue.

For more information on the Center for the Biology of Chronic Disease, or to schedule an interview with Dr. Polansky, please visit http://www.cbcd.net or call 585-250-9999.

The Center for the Biology of Chronic Disease (CBCD, http://www.cbcd.net) is a research center recognized by the IRS as a 501(c)(3) non-for-profit organization. The mission of the CBCD is to advance the research on the biology of chronic diseases, and to accelerate the discovery of treatments for these diseases.

The CBCD published the “Purple” book entitled “Microcompetition with Foreign DNA and the Origin of Chronic Disease” written by Dr. Hanan Polansky. The book presents Dr. Polansky’s highly acclaimed scientific theory on the relationship between the DNA of latent (chronic) viruses and the onset of chronic diseases. Dr. Polansky’s book is available as a free download from the CBCD website.

We invite biologists, virologists, and scientists everywhere to download Dr. Polansky’s book.

###

John S. Boyd, PhD
CENTER FOR THE BIOLOGY OF CHRONIC DISEASE
(585) 250-9999
Email Information

 

Read More…

Gone After Gardasil: Acceptable Collateral Damage? SaneVax Asks: How much damage is acceptable?

By Freda Birrell and Norma Erickson, SaneVax Inc.

According to government health authorities, medical ‘experts,’ and the pharmaceutical industry adverse events after vaccinations are extremely rare. The attitude of these organizations toward individuals who do experience an adverse reaction to vaccines was recently summed up quite clearly in an article titled, The Value of Life, Statistically Speaking by Rick Jones, CFO magazine which stated:

“Inoculating children to prevent infectious disease transmission is good for society from both health and financial perspectives, but some initially healthy children may suffer adverse reactions, injury, or even death. For vaccines, the enormous societal benefits trump the tragedies of the few.”

In other words, those who suffer adverse reactions, injury and even death are viewed as acceptable collateral damage, nothing more than statistics.

Allow us to introduce you to a small sample of the statistically ‘rare’ adverse events after receiving the HPV vaccine, Gardasil:

Jessica Ericzon

Jessie Ericzon:  Jessie was one of those rare individuals who truly had a zest for life. In her universe everyone deserved a fair chance and she made it her personal mission to make sure everyone around her had one. She excelled at everything she tried; truly an individual who had the world by the tail.

All of her hopes and dreams came to an abrupt end on February 22, 2008. That is the day her parents discovered her dead on the bathroom floor a mere 40 hours after her third injection of Gardasil.

Jessie’s parents are left to deal with the fact that their precious daughter is indeed ‘One Less’ woman who will have to deal with cervical cancer.’

Chris Tarsell

Chris Tarsell:  Chris was discovered dead in her college dorm room bed 18 days after her third dose of Gardasil. Her abrupt departure from this world has left a multitude of people wondering what happened to this sweet, spirited, generous and caring individual who had been such a credit to the human race.

Chris’s coroner could not identify a cause of death in this previously healthy girl. Are those left behind supposed to believe some strange, ‘coincidental’ force of nature took her life as alleged by the CDC?

Chris’s death was not thoroughly investigated by the CDC/FDA. One would think they would at least talk with the family to gather information regarding pre- and post-injection symptoms? Shouldn’t they do a statistical analysis of post injection deaths to determine the probability of these deaths being “coincidences”?

Such an analysis was done by Dr. James Garrett in a report posted at www.gardasil-and-unexplained-deaths.com . This report concluded it is statistically untenable to claim that none of the reported deaths was related to Gardasil. Where are the government health agencies charged with protecting the health and safety of the people who pay their wages? Why are they using inadequate data provided largely by the manufacturer to track vaccine safety? Why is the fox guarding the hen house?

Annabelle
Annebelle Morin

Annabelle Morin: Annabelle ended up in the hospital with aphasia (the inability to understand spoken or written words) and great difficulty standing 16 days after her first dose of Gardasil. None of her family knew Gardasil had been administered, so no connection was made between her symptoms and the vaccine. 15 days after her second injection, this 14-year-old, French Canadian girl came home from school, had her dinner and went to take a bath and read a book. Half an hour later, with no warning, she was gone.

Once again, the coroner could not identify a cause of death. Did this spur a complete investigation to find out what may have caused her death? No! Canadian health authorities seem no more concerned than their counterparts in the United States.

One more precious life cut short leaving family, friends and neighbors wondering why no one seems to care what happened. Why is more investigation done for an accidental death than one that no one, including the coroner, can explain?

Jasmine Renata: Jasmine received her first injection of Gardasil in September 2008. One month later, she developed

Jasmine Renata

warts on her hand and very dry skin. The warts were taken care of, but shortly after the second shot, they returned along with bouts of dizziness, numbness and tingling in her hands, abdominal pain and memory losses.

On March 17, 2009, Jasmine got her third and final dose of Gardasil. Her condition quickly deteriorated. She became more agitated, continuing to complain of tingling in her hands and feet, along with various other new symptoms. Her memory losses were so severe she could not remember simple things like how to grate carrots. Shortly after, she began to experience chest pains and rapid heartbeat.

Just a little over 6 months after her third injection of Gardasil, this once healthy, hard-working 18 year-old girl died in her sleep. The 22 of September 2009 was the last day of her life.

Jasmine’s coroner ruled out drug and alcohol abuse as potential causes of her death. But, much like the other girls, no cause of death could be established. How do the health authorities in New Zealand respond when a young woman dies suddenly with no apparent cause? Unfortunately for the Renata family, they responded much like those in the United States and Canada. They do not appear to be concerned – just another coincidence, apparently.

Megan Hild

Megan Hild: At 20 years old, Megan was happy and healthy. She was studying radiology in college and looking forward to her planned marriage after graduation. She held life in the palm of her hand.

Megan was living away from home while attending college, so her mother was not totally aware of the health problems she experienced after taking Gardasil. Megan’s new medical conditions included unexplained rashes, severe stomach pains, migraines, extreme fatigue and vaginal bleeding. Imagine the shock when shortly after speaking with Megan on the phone her precious daughter was found on her knees in the shower of her college apartment – dead. Only after her sudden death would mom discover the new medical conditions Megan had after her Gardasil shots.

Megan’s mother will not have the opportunity to watch her daughter’s dreams come true. She, her family and Megan’s fiancé are left with nothing to hold onto but a piece of paper that reads, “Cause of death, unknown.”

Megan’s mother is still trying to grapple with the belief that a vaccine meant to protect her daughter’s future health may have taken her life. She does not understand why no one in a position to investigate seems to care. She does not understand why health officials appear quite content to allow the cause of Megan’s death to remain ‘undetermined.’

These young women represent a small fraction of those who paid the ultimate price following Gardasil vaccination. It is common knowledge that only 1 to 10% of adverse reactions are actually reported to the Vaccine Adverse Event Reporting System (VAERS). Are these young women representative of 50 other devastated families or, 500 others? No one knows.

Try explaining to those left behind that their loss is acceptable for society’s benefit when the only benefit Gardasil is clinically proven to provide is a 0.6% reduction in HPV 16 infections, and a 1.1% reduction in HPV 18 infections in vaccinated women versus unvaccinated women, providing they were not previously exposed to these two types of HPV prior to being vaccinated. (ATHENA study referenced below)

What about the 108 death reports filed with VAERS after HPV vaccine administration? How many others world-wide do they represent? 1,080? 10,800? Once again, no one knows. At what point does the collateral damage become unacceptable?

Explain to these families why they are left to their own devices if they want to know what caused their child’s death. Had these deaths occurred after the use of any product other than a vaccine, the offending product would have been promptly removed from the market pending the outcome of investigations to determine the cause of the problem.

There is no valid excuse for the situation to be different with vaccines. It is high time for the FDA/CDC and every other government health agency worldwide to man-up and actually do the job they are paid to do – protect public health and safety. Investigate each and every death thoroughly. Determine the causes.

It should not be up to the survivors to prove a causal relationship; it should be up to the manufacturer to show that none exists.

References:

  • http://www.ncbi.nlm.nih.gov/pubmed/21944226 (see table 3, The ATHENA human papillomavirus study: design, methods, and baseline results)
  • Data From Table 3, The ATHENA human papillomavirus study: design, methods, and baseline results

HPV Vaccine Victim’s Advocacy Group Sends Open Letter to HHS Secretary Kathleen Sebelius

InfoWars.com

Curt Linderman Sr.
Infowars.com
February 3, 2012

As of Dec. 2011, there have been 24,610 documented adverse reactions associated with the HPV vaccines, 3,269 have been serious. Given the fact that data from the VAERS (Vaccine Adverse Event Reporting System) database and the National Vaccine Information Center claim that less than 10% of adverse reactions are actually reported, these numbers could be far more frightening.

Sane Vax, an HPV vaccine victim’s advocacy group (www.sanevax.org) recently sent an open letter to HHS Secretary Kathleen Sebelius (1). In this letter and subsequent articles pertaining to HPV Vaccine injuries, it is explained that all drugs given a “fast track” or accelerated approval process through the Food and Drug Administration, are required to verify and prove the fast tracked drug is actually effective and safe through post marketing studies (2). Gardacil was one of those “fast tracked” drugs, despite the fact that I can’t seem to remember the epidemic of young women dropping in the streets, succumbing to cervical cancer. There was no reason to fast track such a vaccine. This kind of tactic should only be available for epidemic and pandemic viruses.

A recently published, and industry sponsored, study (3) conducted on 12,852 young women seems to prove, beyond a reasonable doubt, that HPV vaccines are not working and even seem to be causing cancers! Gardacil and Cervarix, the two HPV vaccines manufactured at this time, only vaccinate for a small number of the human papillomavirus strains and in this study, suggest that HPV vaccination was found to reduce HPV-16 infections by a mere 0.6% in vaccinated vs. unvaccinated women.

Sane Vax states that, in the very same study, 2.6% to 6.2% more HPV vaccinated young women experienced other high risk (carcinogenic) HPV infections than unvaccinated women! When one considers the drastic numbers of adverse reactions, the lack of proof that any post marketing studies are showing success for the vaccines and the outcry from parents regarding draconian measures from governments to force girls (and now boys) to get vaccinated, Secretary Sebellius, the HHS and the FDA should immediately stop the HPV vaccine recommendations and forcibly remove the product from the market.

Why on earth would they continue to mandate these vaccines to our young girls and boys, given the facts that you, the reader, have available now? Given the PAP smears and other gynecological efforts made available to girls around the western world, this vaccine will end up being a nightmare. These girls, believing that the FDA and Secretary Sebellius have done their homework and the vaccine is both safe and effective, will believe they are protected and be less likely to go to the doctor for their checkups. This alone will cost numerous lives. Add to this, the evidence from this most recent study that vaccinated girls are getting more cancers, and you have a recipe for disaster.

Read Full Article…

Gardasil: Dr. Hanan Polansky Explains How the Foreign DNA Fragments Found in the Vaccine can Cause Disease

The FDA asserts that the foreign DNA fragments found in Gardasil pose no risk. In contrast, Dr. Hanan Polansky, from the Center for the Biology of Chronic Disease, uses his highly acclaimed discovery of Microcompetition to explain how these DNA fragments can cause major diseases.

PRWeb

Rochester, New York (PRWEB) February 04, 2012

Gardasil is the FDA approved HPV vaccine. As of September 15, 2011, the Centers for Disease Control (CDC) received a total of 20,096 reports of adverse events in relation to Gardasil vaccination. Dr. Hanan Polansky, Director of the Center for the Biology of Chronic Disease, will discuss his discovery of Microcompetition with Norma Erickson, President of SANE Vax Inc. Dr. Polansky will use Microcompetition to explain the biological mechanism underlying the Gardasil adverse events. Leslie Carol Botha will host the event on the Holy Hormones Radio Show. The show will be broadcast on the community radio station KRFC FM in Fort Collins, CO, Monday, February 6, from 6 to 7pm MST.

Dr. Hanan Polansky is the author of the highly acclaimed “Purple” book, entitled Microcompetition with Foreign DNA and the Origin of Chronic Disease. In his book he explains how foreign DNA fragments can cause many major diseases without damaging (mutating) the human DNA. The book has been read by more than 5,000 scientists around the world, and has been reviewed in more than 20 leading scientific journals.

“Even if only a portion of the author’s (Dr. Hanan Polansky’s) thesis is correct, it would establish wholly new insights into the pathogenesis of chronic disease states, and would have significant implications for treatment and/or prevention.” – Kim E. Barrett, PhD – Professor of Medicine and Vice-Chair for Research, Department of Medicine, University of California, San Diego, School of Medicine.

The FDA says on its website that “Since the early development of Gardasil, FDA and the manufacturer (Merck and Co., Inc.) have known that after purification of the vaccine, small quantities of residual recombinant HPV L1-specific DNA fragments remain in the vaccine.” … “The presence of DNA fragments is expected in Gardasil … these are not contaminants …. The presence of these DNA fragments is expected, is not a risk to vaccine recipients, and is not a safety factor.”

The FDA and Merck admit that Gardasil contains foreign DNA fragments. However, the FDA asserts that these foreign DNA fragments pose no risk. In contrast, Dr. Hanan Polansky, in his highly acclaimed “Purple” book explains how certain foreign DNA fragments, at high concentrations, cause major diseases, such as, cancer, heart disease, diabetes, autoimmune diseases, and even obesity even when the DNA is broken and not functioning.

Read the entire article here.

SaneVax Writes Open Letter to Kathleen Sebelius, Secretary of Health: Rescind approval of Gardasil® due to lack of efficacy during post-licensure monitoring

 

 

 

By Norma Erickson, President.

According to a recently published, industry-sponsored study conducted on 12,852 young women, HPV vaccination was found to reduce HPV-16 infections a mere 0.6% in vaccinated women versus unvaccinated women. At the same time, other high-risk (carcinogenic) HPV infections were diagnosed in vaccinated women 2.6% to 6.2% more frequently than in the unvaccinated women. The increased rate of infections caused by carcinogenic HPV types other than those targeted by Gardasil® in vaccinated women is 4 to 10 times higher than the reduction in HPV 16/18 infections.[1]

These statistics are not exactly encouraging when it comes to demonstrating efficacy for Gardasil®. In fact, quite the opposite – these figures seem to indicate that women who receive Gardasil® may indeed increase their risk of developing cervical cancer from high-risk HPV types that are not targeted by the vaccine.

Medical consumers cannot afford to take the chance of increasing their risk of contracting a disease that has been virtually eradicated by good gynecological care in the United States (cervical cancer) by taking a series of HPV vaccines and hoping they will find out decades later the vaccine worked. It is certainly not a risk children should have to take.

Armed with the knowledge that any drug approved under the FDA’s accelerated approval process using a surrogate endpoint, such as Gardasil®, requires post-marketing studies “to verify and describe the drugs clinical benefit and to resolve remaining uncertainty as to the relation of the surrogate endpoint upon which approval was based to clinical benefit…[2],” the SaneVax Team felt compelled to appeal to the person in charge of FDA/CDC oversight, Kathleen Sebelius, Secretary of Health and Human Services.

On 31 January 2012, SaneVax Inc. sent an open letter to Ms Sebelius[3] asking her to rescind approval for Gardasil® based on the lack of efficacy demonstrated in the ATHENA study referenced above.

If the Department of Health and Human Services is truly interested in public health and safety, they will do the right thing and rescind Gardasil® approval until the manufacturer can provide scientifically sound data proving this new drug is actually effective.

In the meantime, medical consumers around the globe have a choice. Is poke and hope good enough for you and your children? Or, are you going to demand scientific proof of efficacy before submitting to HPV vaccination?

SaneVax open letter to educators worldwide: Watch for side effects of HPV vaccines

Natural News

Tuesday, January 31, 2012 by: Rosemary Mathis, Vice President of Victim Support, SANE VAX, INC.

No one can disagree with the fact that children are the future of the world. Without children, there would be no future. As educators you are responsible for not only teaching young minds, but also for the children’s physical health and well-being for several hours each day.

The SaneVax team knows you take your position seriously. Since the adverse events to be expected after HPV vaccine administration, (GardasilR, CervarixR, or Silgard) are not widely published, we would like to provide you with a list of potential health problems your students may experience after administration of HPV vaccines.

Although the manufacturers say these adverse events are rare, in one clinical trial 73.3% of the trial participants experienced new medical conditions after vaccination. Many of them were quite serious. Any new medical condition experienced after vaccination should be considered a potential adverse effect until proven otherwise.

These conditions are quite frequently attributed to causes other than vaccination; hence delaying necessary medical care. This is particularly true of HPV vaccinations, because the side effects may not show up for months.

The most common side effects of HPV vaccines are pain, swelling, itching, bruising and redness at the injection site, headache, fever, nausea, dizziness, vomiting and fainting.

The following side effects are less common, but more dangerous:

*Difficulty breathing, shortness of breath or wheezing (bronco spasm)
*Hives and/or rash
*Swollen glands (neck, armpit, or groin)
*Joint, leg, or chest pain
*Unusual tiredness, weakness, lethargy, brain fog, or confusion
*Chills
*Generally feeling unwell
*Aching muscles and/or muscle weakness
*Difficulty keeping food down, vomiting or stomach ache
*Seizures
*Shortness of breath
*Chest pain
*Bad stomach pain
*Skin infection
*Bleeding or bruising more easily than normal

This list is by no means comprehensive; it is taken directly from HPV patient Product Information inserts. Many young girls from around the world have experienced many more severe events after HPV vaccination. For the health and safety of the children in your care, please be alert to any changes in your student’s health and behavior post-vaccination.

Should a student experience any of the less common side effect symptoms even months after vaccination, please alert their parents to the possibility that the student may be exhibiting a vaccine reaction, so they can consult their physician for proper medical care.

The SaneVax team would like to thank you for taking care of and watching out for the health and well-being of the students throughout the world.

Norma Erickson, President of SaneVax Inc.
Rosemary Mathis, Vice President, Victim Support
Freda Birrell, Secretary
Leslie Carol Botha, Vice President of Public Relations
Janny Stokvis, Vice President of Research
Linda Thompson, Treasurer

Please visit our site at http://sanevax.org/

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Facts known to vaccinators are not communicated to the consumer

 

January 24, 2012

Letter to the Editor

In October, 2011 “Mercy” has published article by Dr. Joseph Mercola on Gardasil HPV vaccine from Merck produced by the company. A detailed analysis of the history of vaccines, clinical trials, promoting it on the market of pharmaceutical services, data on complications leads to the conclusion that the clinical efficacy of the vaccine and its safety are not only not proven facts, but also cause great doubt. Not to vaccinate their children against HPV, it can destroy the lives of your family – that is the inspiration of Dr. Mercola article. It seems to be told. What made ​​me come back to this topic?

Tracking materials on immunization, I always see pictures of girls, for whom the consequences of vaccination or Gardasilom Cervarix (human papillomavirus vaccine from GlaxoSmithKline company) have severe disability or death. Openly and trustfully look at it this world, a world so familiar and comfortable, because it designed to protect the lives of their adult: mom, dad, school teachers, college professors, the attending physician. The faithful, reliable, armed with professional knowledge, experience wise. They can feel safe. It’s unbearable to think that the adult world so cruelly summed up their children. Seeing the time, you can not forget the gentle face, accept the fact that the photographer captured moments when “still alive”, not to return.

22-year-old graduate of the College of Art in New York, a great athlete, a volunteer charitable programs of the local church, a member of the international organization “Amnesty” Christina Tarsell died in June 2008, 18 days after the third injection Gardasil. In February 2008, at the age of 18 years left cheerful and active Jessica Erickson of New York. It happened 2 days after the third dose of the same vaccine. 20-year-old student Shella Roberts of North Carolina, died in April 2008 after vaccination Gardasilom. At the age of 19 years died of pulmonary embolism on the 14th day after the first injection of Gardasil Brook Petkevitsius of Flordy. Alas, the list of women whose life was tragically cut short due to complications from vaccine injections can be continued. Another long list of those whose early years, and maybe even the whole of life, destroyed severe disabilities following the vaccination Gardasilom or Cervarix.

A nationwide vaccination program began Cervarix in the UK in September 2008. Already in the first year of the program more than 2,000 girls were complications of varying severity. In May 2009 the Sunday Express newspaper reported on 13-year-old Rebecca Ramadzh (Reigate, Surrey), who could not walk for 6 months because of inflammation in the joints. Her doctor had no doubt that the disease was the result of vaccination Cervarix .

A nationwide vaccination program began Cervarix in the UK in September 2008. Already in the first year of the program more than 2,000 girls were complications of varying severity. In May 2009 the Sunday Express newspaper reported on 13-year-old Rebecca Ramadzh (Reigate, Surrey), who could not walk for 6 months because of inflammation in the joints. Her doctor had no doubt that the disease was the result of vaccination Cervarix .

Lucy’s parents thirteen Hincks from Cumbria have heard of cases of complications after vaccination for girls from HPV, but they still decided in favor of vaccination. “I’m worried, because Lucy is very difficult underwent a triple vaccine against measles, rubella and mumps, but the nurse reassured me, assuring that the risk of complications is extremely low – says Pauline Hincks, his mother Lucy – we feel betrayed, because, as most parents, we believed that we can trust our official medicine in matters of life and health of our children. ” After vaccination, Lucy gradually lost the ability to move about the studies we have not discussed, although vaccination was the best girl student of class and won in competitions in mathematics. Lucy is constantly losing weight, sleeping 23 hours a day , and when waking up, then barely whispered a few words “pain in the toilet, tablet, water” and most of all – “Mom”.

Doctors protest, officials do not see a problem

Doctors in different countries look to their committees for vaccination to reconsider a decision to introduce vaccination against HPV immunization program in schools. A number of scientists believe that the alleged 70% protection against cervical cancer is a great exaggeration, and not based on any scientific data. In fact, this manipulation of parents who are trying all means to convince that this vaccination is necessary to their daughters.

In Germany, 13 professors of medicine with an impeccable reputation accused the vaccine manufacturers that they give false information. In particular, Professor Martin Doran (Charity Hospital, Berlin) announces: “Our concern is that the manufacturers of the vaccine manipulated the facts. They claim that the vaccine protects against many strains of the virus that causes cancer, but says nothing about the fact that there is a sufficient number of strains of the same virus from which it does not protect. ” Professor Doran said that the balance of benefits and risks from the vaccine manufacturers is distorted, and special concern is the fact that clinical trials of Cervarix were only in the age group 15 to 26 years. “Vaccinate girls 12-13 years in the absence of data on the safety of the vaccine for this age group is not only wrong from a medical standpoint, but also unethical.”

In the Netherlands, 6 girls were hospitalized after the injection of Cervarix, more than 500 were complications of varying severity. As a result of mass vaccination of resistance caused by its reactogenicity, only 49% of Dutch women made the first of three injections.

In February 2010, 80 000 doses of Cervarix has been withdrawn from hospitals in Valencia and the Balearic Islands after three girls were hospitalized with convulsions and loss of consciousness after a few hours after inoculation.

Unfortunately, neither the health authorities in Spain, nor the officials of Germany did not support the initiatives of their doctors and continue to recommend Cervarix for girls and vaccination of schoolgirls.

In October 2011, three Parisian doctor turned to the National Assembly of France with a call to delete from the list of Gardasil approved for use of drugs and to suspend the certification of the vaccine in Europe, as there are serious doubts about its safety and effectiveness. Gynecologist, Jean-Pierre Spinoza, author of “Why do we vaccinate girls against cervical cancer?” Says Aluminium, contained as an adjuvant in the vaccine Gardasil, is a known neurotoxin, and therefore should not be part of the vaccine. Doctors also find unacceptable the practice of certification of medical products if the administrative authorities of the European Union follow the recommendations of the Administration for quality control and Drug Administration USA (FDA), without conducting its own tests.

The conflict between the policy of silence and evidence-based medicine

December 22, 2011 in the “Annals of Medicine” appeared Tomlenovich article Lucy and Christopher Shaw , scientists from the University of British Columbia (Vancouver, Canada), “Human papillomavirus: the conflict between the policy of vaccination and evidence-based medicine?” That’s what Canadian experts wrote: “Methods of promotion HPV vaccine shows that are not always facts known vaccinators will be communicated to the consumer. For example, the world’s leading medical organizations claim that a vaccine against HPV is an important tool to prevent cervical cancer, while there were no such clinical trials that would demonstrate that the vaccine actually protects against cancer. Further, in contrast to the assertion that cervical cancer is the second most common type of cancer among women worldwide, real-world data suggest that this is true only for developing countries. In the Western world, cervical cancer is a rare disease with mortality rates several times lower than the level registered in the system of notification of serious complications (including fatal cases) from those considered vaccines. Future vaccination strategies should be firmly rooted in evidence-based medicine and the ethical principle of informed consent. “

In his article, Dr. Mercola gives the list of complications after vaccination Gardasilom. The list is not complete, but, nonetheless, impressive. And here is a new and absolutely astonishing fact : the American system of warning about the complications of vaccination (VAERS) from August to December 2011 among 24 601 Complications of Gardasil registered 471 cases of deviation from the norm in the analysis for HPV, 181 cases of cervical dysplasia (precancerous state) and 47 cases of cervical cancer! That is, complications from vaccination are those very diseases from which she, according to the manufacturers and public health agencies, provides reliable protection.

Health activists from the organization Sane Vax, Inc. (“For a reasonable vaccination”) decided to conduct its own investigation . They took 13 vials of Gardasilom from different parties, to be sold in the United States, Australia, New Zealand, Spain, France and Poland. Laboratory analysis showed that all 13 doses of recombinant DNA of HPV. In September 2011 Norma Erickson, president of Sane Vax, sent a letter to the U.S. Administration for Quality Control of Food and Drug Administration (FDA) c to draw their attention to this fact as a possible cause of serious complications after vaccination Gardasilom, such as leukemia, lymphoma, rheumatoid arthritis, human papillomavirus infection as such, a cancer of the cervix. “The 13-year-old girl, sexually innocent, 24 hours after the third injection Gardasil developed symptoms of rheumatoid arthritis, and two years later when the blood test it was discovered papillomavirus – wrote Erickson – because 100% of the samples contained HPV DNA, Sane Vax, Inc. asked the Administration for Quality Control of Food and Drug Administration to investigate the extent of infection already on the market, lots of vaccine Gardasil and take measures to ensure the security of future supplies of vaccine. ”

In his reply to Norma Erickson on September 23, 2011 Head of Relations with consumers Walter Gardner reported that the presence of recombinant DNA of HPV in the vaccine Gardasil is to be expected and not harmful to the recipients. Also, the FDA had not heard, not seen and do not know anything about the connection of child rheumatoid arthritis vaccine against HPV.

Most of all, the answer affects the calculation that the policy of double default in some way can transform a lie into the truth and thus convince the recipient. But if you believe that recombinant DNA is not a risk factor, then why in the documents to the FDA and the manufacturer’s information leaflet (Norm Erikson cites official documents of the number 8) states that Gardasil “does not contain the DNA of the virus?” If we are talking exclusively about the natural DNA, not recombinant, then why in the information leaflet for the vaccine does not indicate that Gardasil, among others, contains the components of the recombinant DNA of HPV? And how about the fact that in the patent US № 6,602,697, issued to Merck on Gardasil, it is argued that the vaccine free of biomolecules, including the DNA, lipids and proteins? Why is it that the FDA, according to the text message of Mr. Gardner, do not know about that as a result of clinical trials of Gardasil found that vaccinated patients fell ill with rheumatoid arthritis is 3 times more likely than patients of the control group? But this is data from the manufacturer, not from the registration system complications. After that, not surprisingly, that health officials are not familiar with the research, describing “the mechanism of virus free delivery of the gene” , which is triggered by ingestion of human recombinant DNA. Enough integration of a single functional unit of the foreign DNA into the cellular genome of the recipient in order to began the transformation of cells. But apparently, the officials did not read the medical literature and believe (or pretend to believe) that the recombinant DNA of the virus does not pose a risk to those they will be introduced in the vaccine.

And what about us?

And we have – best of all. The value of pi in our country comes up to 4, the number of voters at polling stations – up to 146%, and the effectiveness of Gardasil, according to the information of medical centers offering vaccination against human papillomavirus, is practically equal to 100%.

As mentioned above, scientists believe that 70 percent efficiency, according to the manufacturer , is a great exaggeration. But no, we have 100%.

Vaccination against HPV is not included in the RF schedule immunizations for school children, and besides, she is paid to patients. Because of this coincidence, Gardasil and Cervarix have not so far that no binding, nor popular. No exact statistics, but apparently, the percentage of grafted these vaccines in Russia has been slow. But things can change very quickly: first, Cervarix will soon begin to produce in Russia outside Moscow at the facilities of CJSC “Binnofarm” , and secondly, the intention is to high health officials to introduce this vaccine in the childhood vaccination schedule.

I am very anxious for our children.

 

Marina Solodovniko

Original Article Here…. http://miloserdie.ru/index.php?ss=1&s=8&id=16583

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