"All the World's a Stage We Pass Through" – R. Ayana

Tuesday, 2 February 2016

Another High-profile Global Vaccine Conspiracy Exposed — This Time It’s the HPV Vaccine


Another High-profile Global Vaccine Conspiracy Exposed —
This Time It’s the HPV Vaccine

Vaccine




As a researcher who’s been tracking vaccine issues, including scientific hijinks, since the 1980s, I cannot express what a pleasure it is to report the following unfolding vaccine geo-political drama. This alleged conspiratorial action is about the fourth or fifth one to break into daylight.

Others include: the Simpsonwood Meeting [1] (June 2000); the Danish/CDC-paid vaccine researcher Dr. Poul Thorson who has been indicted for defrauding the U.S. CDC regarding research he produced from 2000 to 2009 [2]; the William Thompson, PhD, CDC epidemiologist who admits that CDC researchers deliberately omitted, and even trashed, incriminating data sets regarding vaccines impact on young black males under 3 years of age [3]; and let’s not forget a whistleblower lawsuit in federal court in Philadelphia, PA wherein two former Merck & Company employees claim Merck falsified efficacy rates for many years for the mumps active in its MMR vaccine [4].

While nothing seemingly has been done either legally or professionally to hold accountable government officials and scientists, plus those who have colluded with them to perpetrate vaccine and scientific frauds on humanity up until now, let’s make certain the alleged conspiracy I’m going to report about is not swept into a convenient memory hole or under a bureaucratic ‘consensus science’ carpet of Big Pharma’s “old boy network.”

What I’m about to report is taken directly from copies of documents I have in my possession. There’s no Photoshop stuff going on here. This is the real McCoy! I have in my possession copies of numerous emails—obtained via FOIA New Zealand—that were sent by, received or copied to the following individuals with regard to the allegations Dr. Sin Hang Lee puts forth in his January 14, 2016 complaint to the Director-General of the World Health Organization, Dr. Margaret Chan:

  • Helen Petousis-Harris (PhD, MRSNZ) Director of Immunisation Research and Vaccinology, University of Auckland (New Zealand)
  • Robert Pless (MD, MSc), Chairperson of GACVS (Public Health Agency of Canada)
  • Dr. Koji Nabae, Deputy Director, Ministry of Health, Labour & Welfare, Government of Japan
  • Patrick Louis F. Zuber, WHO—Global Vaccine Safety Initiative, Dept. of Essential Medicines & Health Products, Geneva, Switzerland
  • Melinda Wharton (MD, MPH) United States CDC/OID/NCIRD
  • Isabelle Sahinovic, Technical Officer, WHO Secretariat to the Global Vaccine Safety Initiative
  • Philipp Lambach, Medical Officer, WHO Secretariat to the Global Vaccine Safety Initiative

 

 

What is the GACVS?

 

It’s the Global Advisory Committee on Vaccine Safety within the World Health Organization.

Who are the members of GACVS? No individual names could be found from online searches I did. However, according to GACVS’s website, it “provides independent, authoritative, scientific advice to WHO [World Health Organization] on vaccine safety issues of global or regional concern with the potential to affect in the short or long term national immunization programmes.”

GACVS purportedly “determines causal relationships between vaccines and/or their components and adverse events attributed to them,” which its members obviously did not respect nor comply with relative to the HPV vaccine Gardasil® testimony alleged advance preparation collusion leading up to the hearing February 26, 2014, held under the auspices of the Japanese Ministry of Health, Labour & Welfare, in Japan.

Allegedly remiss by its actions, GACVS members are alleged to have colluded to NOT “evaluate appropriate methodological and empirical research on any purported association between specific vaccines/vaccine components and adverse event(s)…” [5], which is documented in the 16-page open-letter-complaint to the General Director of WHO, Dr. Margaret Chan, filed by the Director of Milford Molecular Diagnostics Laboratory, Dr. Sin Hang Lee, MD. Furthermore, Dr. Lee was one of the medical researchers who testified on February 26, 2014 at the Ministry of Health hearing [5]. Here’s my blog about that meeting.

Fast forward to uncovering what’s developed in the world of scientific mischief.

 

According to the complaint Dr. Lee filed January 14, 2016, “multiple individuals and organizations deliberately set out to mislead Japanese authorities regarding the safety of the human papillomavirus (HPV) vaccines, Gardasil® and Cervarix®, which were being promoted at that time.” Dr. Lee goes on to say,

Should the information in this letter [16 pages] prove to be accurate, nothing short of an Immediate independent investigation resulting in appropriate disciplinary actions for those involved will be able to restore the public trust. Therefore, I implore you to act quickly and decisively regarding this critical public health issue.

As part of his introduction, Dr. Lee cites the names of individuals involved [Pless, Nabae, Wharton, Petousis-Harrs, including WHO GACVS officials] who “may have been actively involved in a scheme to deliberately mislead the Japanese Expert Inquiry on human papillomavirus (HPV) vaccine safety before, during and after the February 26, 2014 public hearings in Tokyo.”

 

What’s it all about?

 

Dr. Lee believes “the information supplied by this group led directly to the issuance of the GAVCS [sic] statement on the continued safety of HPV vaccination on March 12, 2014 which contains the following paragraph:

Several papers have also been published pertaining to the finding of HPV L1 gene DNA fragments in clinical specimens following HPV vaccination [13, 14]. These papers claimed an association with clinical events of an inflammatory nature, including cerebral vasculitis. While the GACVS has not formally reviewed this work, both the finding of DNA fragments in the HPV vaccine and their postulated relationship to clinical symptoms, have been reviewed by panels of experts. First, the presence of HPV DNA fragments has been addressed by vaccine regulatory authorities who have clearly outlined it as an expected finding given the manufacturing process, and not a safety concern [15]. Second, the case reports [13] of adverse events hypothesized to represent a causal association between the HPV L1 gene DNA fragments and death were flawed in both clinical and laboratory methodology [16]. The paper described 2 fatal cases of sudden death in young women following HPV vaccine, one after 10 days and one after 6 months, with no autopsy findings to support death as result of cerebral vasculitis or an inflammatory syndrome. Thus the hypotheses raised in these papers are not supported by what is understood about the residual DNA fragments left over following vaccine production [17]: given the extremely small quantities of residual HPV DNA in the vaccine, and no evidence of inflammation on autopsy, ascribing a diagnosis of cerebral vasculitis and suggesting it may have caused death is unfounded.” (the references 13-17 quoted were those listed in the GACVS Statement)

 

Is a scientific web of deceit being spun to validate a scientific non sequitur?

 

Dr. Lee explains in no uncertain scientific terms what the alleged collaborators apparently had trouble with:

‘Several papers have also been published pertaining to the finding of HPV L1 gene DNA fragments in clinical specimens following HPV vaccination [13,14]’ was apparently constructed for dissembling and designed to mislead, referring to the Tomljenovic and Shaw paper “Vaccination: Causal or Coincidental?” Pharmaceut Reg Affairs 2012, S12:001 about HPV L1 VLPs.

Lee declares, “The authors of reference 13 never mentioned HPV L1 gene DNA fragments at all.” [Something is beginning to smell a little scientifically fishy.]

Apparently, Dr. Pless knew the difference between HPV L VLPs and HPV L1 gene DNA fragments because he addressed his concerns to others involved in the snowballing scheme, especially to Dr. Petousis-Harris, when he said “statement regarding alleged role of aluminum biding to DNA fragments and subsequent effects” in his February 18, 2014 email. Lee claims that “One cannot help but conclude that Dr. Pless intentionally put these two unrelated articles together and claimed that both articles studied HPV L1 gene DNA fragments in order to mislead the non-scientific readers and vaccination policy makers.” [Whoa!]

Furthermore, Lee goes on to challenge this:

‘These papers claimed an association with clinical events of an inflammatory nature, including cerebral vasculitis’ is not true because the author in reference 14 (Lee, SH. Detection of human papillomavirus L1 gene DNA fragments in postmortem blood and spleen after Gardasil® vaccination—A case report. Advances in Bioscience and Biotechnology, 2012, 3, 1214-1224) never claimed clinical events of an inflammatory nature, including cerebral vasculitis. Dr. Pless in fact misstates the author’s words in this document apparently to create a target to attack. [Hmmm!]

No Docturds by R. Ayana

 

If the facts don’t fit, how about just changing them?

 

According to Dr. Lee, “The purpose of Dr. Pless intentionally combining two unrelated studies and two unrelated chemicals show up in the following sentence: ‘the finding of DNA fragments in the HPV vaccine and their postulated relationship to clinical symptoms, have been reviewed by panels of experts.’ Who were these panels of experts? Dr. Pless presented none of their names.” [Okay! What don’t I understand here?!]

Furthermore according to Lee, “’Second, the case reports [13] of adverse events hypothesized to present a causal association between the HPV L1 gene DNA fragments and death were flawed in both clinical and laboratory methodology [16],’ is a blatant misrepresentation of the facts. The authors quoted in Reference #13 never presented any data on HPV L1 gene DNA fragments. Reference #16 never reviewed the potential harm of HPV L1 gene DNA fragments in the HPV vaccines when injected into humans.” [Gotcha!]

 

A plea for help—anyone—PLEASE!

 

Now, here’s where Dr. Lee feels that Dr. Pless could not find any scientific reviews on the HPV L1 gene DNA fragments in HPV vaccines, as illustrated in the email Pless sent to Dr. Petousis-Harris on February 18, 2014 along with a plea for help:

We are seeking your advice on someone who may be able to address the more detailed questions around HPV DNA – specifically the hypotheses you have address [sic] in your statement regarding the alleged role of aluminum binding to DNA fragments and subsequent effects. While the issue of whether the fragments constitute ‘contamination’ has been dealt with, your statement was the only one to address the more obscure alleged consequences of the presence of those fragments. The GACVS has not yet had a chance to delve into the DNA question.

Now here’s where the wicket gets even stickier.

 

Lee says, “The FDA declaration confirming HPV DNA fragments in Gardasil® as an expected finding (Ref.15), but providing no safety data on these HPV DNA fragments after being injected into animals or humans, obviously does not represent a review by panels of experts because it does not refer to any animal or human experimental data on ‘aluminum binding to DNA fragments and subsequent effects,’ which was supposed to be Dr. Pless’ major concern.”

So, what happens next is scientific “pie-in-the-sky,” I’d conjecture.

 

Dr. Petousis-Harris apparently had the chutzpah to try to demonstrate to Dr. Pless that she had experience using similar procedures, when in her February 18, 2014 email to him, she said,

To the best of my knowledge the rebuttal on our website is the only attempt to address this particular issue which Shaw and Lee presented at a coronal enquiry here. Placing the rebuttal in the public domain was the only means of providing the information to the crown representatives involved in that process at the 11th hour. [Really!?]

The plot thickens.

 

Under pressure to issue some type of statement before the public hearing in Japan, Dr. Pless had to find a panel of experts to “declare the safety of aluminum bound to DNA fragments after being injected into humans.” Isn’t that like trying to prove the world is square and not a round globe? So what did they rely on?

The only publication remotely related to the subject Pless could use, according to Lee, was Reference #16, a Clinical Immunization Safety Assessment (CISA) Network Technical Report titled “Review of a published report of cerebral vasculitis after vaccination with the Human Papillomavirus (HPV) Vaccine” dated November 9, 2012.

There was a likely technical flaw in that report, though: That CDC report had unnamed authors, which should have disqualified it from being published as a valid scientific paper, in my opinion, but apparently not according to the CDC’s scientific wisdom. That document had a purpose—apparently to question the data on HPV-16 L1 particles, never HPV L1 gene DNA fragments because the Lee paper reporting the finding of HPV L1 gene DNA fragments (Lee, SH. Detection of human papillomavirus L1 gene DNA fragments in postmortem blood and spleen after Gardasil® vaccination—A case report. Advances in Bioscience and Biotechnology, 2012, 3, 1214-1224) – get this – was not published until December 27, 2012, one and a half months after the CISA Network Technical Report was issued.

No peer review credibility—what next to do?

 

Dr. Lee offers that the CISA report (Reference #16) with unnamed authors began with the following paragraph:

Recently there was discussion on a federally-sponsored vaccine safety listserv of a report in the literature of cerebral vasculitis after vaccination with the Human Papillomavirus Vaccine (HPV) (Tomljenovic L, Shaw CA. Death after Quadrivalent Human Papillomavirus (HPV) Vaccination: Causal or Coincidental? Pharmaceutical Regulatory Affairs: Open Access 2012,S12:001). To address questions about the findings and conclusions reported in this manuscript, CDC convened a CDC-Clinical Immunization Safety Assessment (CISA) working group. Researchers from Vanderbilt Medical Center, Johns Hopkins University, Columbia University, Duke Clinical Research Institute (Duke University), CDC and FDA participated in the call.

That report was the only Technical Report issued in the last 12 years, according to Lee, that has NEVER been published in peer-review journals. Why? Did they know they couldn’t deal with the scientific challenges it would offer? The Disclaimer at the end of that report, I think, says it all:

The information and conclusions in this report are those of the work group participants addressing this issue and do not necessarily represent the official position of CDC.

You have to give credit when credit is due: CDC realized it was in a “check-mate” position. It apparently was a sham report and, as Dr. Lee offers, was written by unnamed ghost writers based on phone conversations. Is that the way science is done? That apparently beats computer modeling.

Dr. Pless was up a scientific tree, out on a limb and had no choice but to misbrand two unrelated articles and two unrelated chemicals in the vaccine Gardasil® in order for his ability to use the CISA Network Technical Repot on HPV-16 L1 particles to support his declaration of safety of HPV L1 gene DNA fragments after injection into humans. However, Dr. Lee offers that Pless had to make policy makers believe that “HPV-16 L1 particles” were synonymous to “HPV L1 gene DNA fragments” in chemistry. Lee says that once that was done, Pless apparently thought he could use the opinion on HPV-16 L1 particles to uphold the safety of HPV L1 gene DNA fragments bound to aluminum adjuvant.

Unable to find a scientific report in published peer review journals, Dr. Pless shrewdly had to MISQUOTE the CISA report on HPV-16 L1 particles as evidence to support Dr. Petousis-Harris’ blog published on SOCIAL MEDIA as he wrote in the GACVS statement:

Thus the hypotheses raised in these papers are not supported by what is understood about the residual DNA fragments left over following vaccine production [17].

And why did Dr. Pless say that?

 

Dr. Petousis-Harris was the author of Reference 17. She was the only writer brave enough to claim publicly “extremely small quantities of residual HPV DNA in the vaccine” to be harmless without any supportive data, according to Dr. Lee. Dr. Pless questions Petousis-Harris in his February 18, 2014 email saying,

A meeting has recently been organized in Tokyo for February 26th, where Dr. Lee will present his findings…

…We are seeking your advice on someone who may be able to address the more detailed questions around HPV DNA – specifically the hypotheses you have address [sic] in your statement regarding the alleged role of aluminum binding to DNA fragments and subsequent effects. While the issue of whether the fragments constitute “contamination” has been dealt with, your statement was the only one to address the more obscure alleged consequences of the presence of those fragments. The GACVS has not yet had a chance to delve into the DNA question.

Dr. Petousis-Harris accepted the role and assignment of presenting at the Tokyo hearing. On February 18, 2014, after receiving Pless’s email, she wrote back and copied several others too. Take note of who they are.

From: Helen Petousis-Harris [mailto:h.petousis-harris@auckland.ac.nz] Sent: Tuesday, February 18, 2014 5:19 AM To: ‘Robert Pless’ Cc: Robert Pless (Robert.Pless@phac-aspc.gc.ca); 難波江 功二(nabae-koji); ZUBER, Patrick Louis F.; Wharton, Melinda (CDC/OID/NCIRD) Subject: RE: URGENT: Regarding the posted commentary on the coronial inquiry expert witness testimony

“Dear Rob Oh dear! I am so saddened to hear how extensive the impact of Lee, Shaw and Tomljenovic’s activities has become. I will certainly do anything I can to assist. [Is this a conspiracy/collusion confirmed in writing?] To the best of my knowledge the rebuttal on our website is the only attempt to address this particular issue which Shaw and Lee presented at a coronal enquiry here. Placing the rebuttal in the public domain was the only means of providing the information to the crown representatives involved in that process at the 11th hour. Prof David Gorsky has written prolifically on some of the experiments in his science blog over the past few years so I assume he has also given the material some thought.

“I do not know if I am expert on this but certainly have some experience in considering aluminium in vaccines and its role in inflammatory responses and local AEFI as part of my PhD some years ago. I assume you are referring to the VLP tightly bound to the adjuvant and the Shaw and Tomljenovic ‘hypothesis’ that it somehow finds its way to the brain carried by macrophage?” [CJF emphasis added]

 

When an expert witness isn’t an expert witness.

 

Dr. Petousis-Harris’s email above obviously indicates that she’s out of her realm of expertise and that she had absolutely no idea or clue as to what Pless wanted her to address at the February 26, 2014 public hearing in Japan. [OMG!] Dr. Lee points out that she apparently and mistakenly assumed she was being asked to comment on “the VLP tightly bound to the adjuvant.” Now here’s an expert witness’s conundrum: Petousis-Harris did not know that VLP is a protein, which cannot be tightly bound to the aluminum adjuvant as the DNA molecules can—so says Dr. Lee.

Holy moly! What an expert witness—but that’s the way consensus science apparently is done, folks!

Furthermore, Petousis-Harris’s qualification was that she had written a social media blog much like Professor David Gorski had done. He’s an apparent well-known online “character assassin” masquerading as a science defender according to Dr. Lee’s complaint letter to Dr. Chan. But Petousis-Harris lauds his work with this,

Prof David Gorsky has written prolifically on some of the experiments in his science blog over the past few years so I assume he has also given the material some thought.

Dr. Pless obviously found himself between a scientific rock and a legal hard place. He knew that the CISA Network Technical Report of November 2012 did not address the presence of HPV L1 gene DNA fragments in the vaccine Gardasil® so he wrote this to Dr. Petousis-Harris,

…We are seeking your advice on someone who may be able to address the more detailed questions around HPV DNA – specifically the hypotheses you have address [sic] in your statement regarding the alleged role of aluminum binding to DNA fragments and subsequent effects. While the issue of whether the fragments constitute “contamination” has been dealt with, your statement was the only one to address the more obscure alleged consequences of the presence of those fragments. … [CJF emphasis added]

It would seem that Petousis-Harris is now in the same position as the “dog that caught the bus.” What do I do now, since my expertise regarding HPV L1 gene DNA fragments is writing on social media blogs and not in peer-review journals?

 

What is “Plan B”?

 

Numerous emails traveled among those involved in this apparent collusion until finally Dr. Koji Nabae of the Japanese government wrote to those listed at the very beginning of this article, the following:

I talked to my boss and we agree that it is better not to have WHO GACVS presence during the public hearing session [numerous words redacted, i.e., blacked out and unreadable] and there is no need to hurry for a statement. We are hoping the statement to come out a week or two weeks later so that our expert committee can refer to it when they finalize the report in March (or a bit later) (if things go smoothely [sic]) [CJF emphasis added]

Was Dr. Nabae, a Japanese government official who presided at the February 26, 2014 public hearing, also colluding with potential witnesses at WHO GACVS in order to avoid cross-examination and scrutiny at the forthcoming hearing?

Dr. Lee, in his complaint, makes this most incriminating of comments, I think:

I believe this maneuver was orchestrated by the Chairperson of the WHO GACVS and others as nothing more than a very cunning means of avoiding having to supply scientific evidence to decision makers. Actions like this corrupt the entire concept of science-based medicine.

Unbelievable at it may sound, Dr. Helen Petousis-Harris was selected as the spokesperson for the Tokyo public hearing. However, someone attached a ‘leash’ on to her PowerPoint presentation, which had to be reviewed by the group before the hearing to ensure she presented the proper message. However, not everyone was satisfied.

Dr. Nabae was concerned about one of the PP slides which stated “immune activation on uptake of HPV vaccine does not include an increase of inflammatory factors (incl TNF) even in vaccinees with large injection site reactions at time of local inflammation” because such claim contradicted the data presented by another expert at their previous meeting which in fact confirmed that cytokines following vaccines increased particularly at injection site after Cervarix® compared to other vaccines (including tumor necrosis factor –TNF), per Dr. Lee! Dr. Nabae also deleted some questionable “Japanese Wildcard” data from the PowerPoint slides to be presented at the hearing. What are Japanese Wildcard data? Does the U.S. CDC/FDA also have wildcard data? How about Big Pharma? I guess they probably may have some Jokercard data too.

 

Petousis-Harris PowerPoint Presentation

 

This is a direct quote from Dr. Lee’s complaint letter:

The Powerpoint slides Dr. Helen Petousis-Harris presented at the public hearing claimed Dr Lee’s case report had no controls to prove that unvaccinated New Zealand teenage girls do not have HPV DNA in non-B conformations in their blood, therefore the findings are not scientifically valid. She said, ‘There are no controls used (unvaccinated). This is a vital part of the scientific process.’ [original emphasis.]

Dr. Helen Petousis-Harris evidently does not understand the difference between a case report and a clinical trial; nor does she seem to know how hard it is for pathologists to find any HPV DNA in blood samples of patients, even those known to have HPV infections, let alone HPV DNA in non-B conformations. This shows how little, if any, experience she has in laboratory medicine.

I find Dr Petousis-Harris blog [6] which was quoted as Ref. 17 by Dr Pless in the GACVS statement in support of the declaration of HPV vaccination safety, to be more concerned with character assassination than in disputing the science of HPV L1 gene DNA fragments in Gardasil® or in postmortem materials.

So much for expert witnesses and science-based medical research, especially when it comes to vaccines!

Dr. Lee asserts that Dr. Petousis-Harris used her PhD thesis as the authoritative research to support her theory of “No elevation of any cytokine associated with reactogenicity.” Is that how consensus, science-based-medicine is pushed in journals and on to healthcare consumers regarding vaccinology?

The emails – and there are close to 236 pages of them, many with lots of redactions – confirm the ongoing collusion among various individuals at WHO, GACVS, and vaccine researchers in other countries’ health agencies. I always have to wonder what’s been redacted and why they wouldn’t want anyone to see redactions. Good question?

Dr. Lee, in summarizing his opinions in his complaint letter, talks about those emails. He says,

[T]his group of WHO officials and government employees charged with the responsibility to advise the expert committee of the Japanese government on HPV vaccination safety knew before the February 26, 2014 Tokyo public hearing that one of their own experts showed scientific evidence that HPV vaccination does increase cytokines, including tumor necrosis factor (TNF), particularly at the injection site compared to other vaccines. Yet, they chose to suppress this information at the public hearing.

It is my contention these people have not only violated the Terms of Reference of the WHO Global Advisory Committee on Vaccine Safety (GACVS); they have violated the public trust. Immediate, independent and thorough investigations into their actions with appropriate disciplinary action is the only option available that might restore the public’s confidence in worldwide health authorities.




The above is as patently obvious as it can be, as to what goes on regarding vaccine science that ‘validates’ toxic vaccines ‘safety’, which are mandated to be given to neonates, infants, toddlers, teens, adults and senior citizens.

Vaccines harm and even kill [7,8], especially the HPV vaccines given to pre-teenage boys and girls [9]. Healthcare consumers need to become “proactive,” as the saying goes.

May I suggest that readers send this information to your members of the U.S. Congress; your individual states legislators in your state capitols; your public health agency department head for your state; your local media—radio, TV, and newspapers; and demand prosecution for scientific/medical fraud crimes committed against children, in particular, in the name of sham vaccine science. You can use this information and the reference links below as documentable proof of what’s going on that no one is questioning and holding accountable.

Furthermore, email a letter about how you feel regarding mandatory vaccines to the people Dr. Sin Hang Lee emailed his 16-page complaint:



References:



Resources:

The Public Hearing on Adverse Events following HPV vaccine in Japan
http://www.mhlw.go.jp/stf/shingi/0000048229.html


Allegations of Scientific Misconduct by GACVS (16-page PDF)

HPV Vaccine Safety Illusion 01.2016 (2 – page PDF)

Catherine J Frompovich (website) is a retired natural nutritionist who earned advanced degrees in Nutrition and Holistic Health Sciences, Certification in Orthomolecular Theory and Practice plus Paralegal Studies. Her work has been published in national and airline magazines since the early 1980s. Catherine authored numerous books on health issues along with co-authoring papers and monographs with physicians, nurses, and holistic healthcare professionals. She has been a consumer healthcare researcher 35 years and counting.
Catherine’s latest book, published October 4, 2013, is Vaccination Voodoo, What YOU Don’t Know About Vaccines, available on Amazon.com.
Her 2012 book A Cancer Answer, Holistic BREAST Cancer Management, A Guide to Effective & Non-Toxic Treatments, is available on Amazon.com and as a Kindle eBook.
Two of Catherine’s more recent books on Amazon.com are Our Chemical Lives And The Hijacking Of Our DNA, A Probe Into What’s Probably Making Us Sick (2009) and Lord, How Can I Make It Through Grieving My Loss, An Inspirational Guide Through the Grieving Process (2008)




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Monday, 1 February 2016

What’s the Truth About the Zika Virus?


What’s the Truth About the Zika Virus?

Zika Outbreak Epicenter in Same Area Where GM Mosquitoes Were Released in 2015

 

http://cdn.theantimedia.org/wp-content/uploads/2016/01/zika-virus-21.jpg




The World Health Organization announced it will convene an Emergency Committee under International Health Regulations on Monday, February 1, concerning the Zika virus ‘explosive’ spread throughout the Americas. The virus reportedly has the potential to reach pandemic proportions — possibly around the globe. But understandingwhy this outbreak happened is vital to curbing it. As the WHO statement said:

“A causal relationship between Zika virus infection and birth malformations and neurological syndromes … is strongly suspected. [These links] have rapidly changed the risk profile of Zika, from a mild threat to one of alarming proportions.

“WHO is deeply concerned about this rapidly evolving situation for 4 main reasons: the possible association of infection with birth malformations and neurological syndromes; the potential for further international spread given the wide geographical distribution of the mosquito vector; the lack of population immunity in newly affected areas; and the absence of vaccines, specific treatments, and rapid diagnostic tests […]

“The level of concern is high, as is the level of uncertainty.”

Zika seemingly exploded out of nowhere. Though it was first discovered in 1947, cases only sporadically occurred throughout Africa and southern Asia. In 2007, the first case was reported in the Pacific. In 2013, a smattering of small outbreaks and individual cases were officially documented in Africa and the western Pacific. They also began showing up in the Americas. In May 2015, Brazil reported its first case of Zika virus — and the situation changed dramatically.

Brazil is now considered the epicenter of the Zika outbreak, which coincides with at least 4,000 reports of babies born with microcephaly just since October.


zika-microcephaly 

When examining a rapidly expanding potential pandemic, it’s necessary to leave no stone unturned so possible solutions, as well as future prevention, will be as effective as possible. In that vein, there was another significant development in 2015.

Oxitec first unveiled its large-scale, genetically-modified mosquito farm in Brazil in July 2012, with the goal of reducing “the incidence of dengue fever,” as The Disease Daily reported. Dengue fever is spread by the same Aedes mosquitoes which spread the Zika virus — and though they “cannot fly more than 400 meters,” WHO stated, “it may inadvertently be transported by humans from one place to another.” By July 2015, shortly after the GM mosquitoes were first released into the wild in Juazeiro, Brazil, Oxitec proudly announced they had “successfully controlled the Aedes aegypti mosquito that spreads dengue fever, chikungunya and zika virus, by reducing the target population by more than 90%.”

Though that might sound like an astounding success — and, arguably, it was — there is an alarming possibility to consider.

Nature, as one Redditor keenly pointed out, finds a way — and the effort to control dengue, zika, and other viruses, appears to have backfired dramatically.


zika
Juazeiro, Brazil — the location where genetically-modified mosquitoes were first released into the wild.

zika
Map showing the concentration of suspected Zika-related cases of microcephaly in Brazil.


The particular strain of Oxitec GM mosquitoes, OX513A, are genetically altered so the vast majority of their offspring will die before they mature — though Dr. Ricarda Steinbrecher published concerns in a report in September 2010 that a known survival rate of 3-4 percent warranted further study before the release of the GM insects. Her concerns, which were echoed by several other scientists both at the time and since, appear to have been ignored — though they should not have been.

Those genetically-modified mosquitoes work to control wild, potentially disease-carrying populations in a very specific manner. Only the male modified Aedes mosquitoes are supposed to be released into the wild — as they will mate with their unaltered female counterparts. Once offspring are produced, the modified, scientific facet is supposed to ‘kick in’ and kill that larvae before it reaches breeding age — if tetracycline is not present during its development. But there is a problem.


zika-mosquito
Aedes aegypti mosquito. Image credit: Muhammad Mahdi Karim


According to an unclassified document from the Trade and Agriculture Directorate Committee for Agriculture dated February 2015, Brazil is the third largest in “global antimicrobial consumption in food animal production” — meaning, Brazil is third in the world for its use of tetracycline in its food animals. As a study by the American Society of Agronomy, et. al., explained, “It is estimated that approximately 75% of antibiotics are not absorbed by animals and are excreted in waste.” One of the antibiotics (or antimicrobials) specifically named in that report for its environmental persistence is tetracycline.

In fact, as a confidential internal Oxitec document divulged in 2012, that survival rate could be as high as 15% — even with low levels of tetracycline present. “Even small amounts of tetracycline can repress” the engineered lethality. Indeed, that 15% survival rate was described by Oxitec:

“After a lot of testing and comparing experimental design, it was found that [researchers] had used a cat food to feed the [OX513A] larvae and this cat food contained chicken. It is known that tetracycline is routinely used to prevent infections in chickens, especially in the cheap, mass produced, chicken used for animal food. The chicken is heat-treated before being used, but this does not remove all the tetracycline. This meant that a small amount of tetracycline was being added from the food to the larvae and repressing the [designed] lethal system.”

Even absent this tetracycline, as Steinbrecher explained, a “sub-population” of genetically-modified Aedes mosquitoes could theoretically develop and thrive, in theory, “capable of surviving and flourishing despite any further” releases of ‘pure’ GM mosquitoes which still have that gene intact. She added, “the effectiveness of the system also depends on the [genetically-designed] late onset of the lethality. If the time of onset is altered due to environmental conditions … then a 3-4% [survival rate] represents a much bigger problem…”

As the WHO stated in its press release, “conditions associated with this year’s El Nino weather pattern are expected to increase mosquito populations greatly in many areas.”

Incidentally, President Obama called for a massive research effort to develop a vaccine for the Zika virus, as one does not currently exist. Brazil has now called in 200,000 soldiers to somehow help combat the virus’ spread. Aedes mosquitoes have reportedly been spotted in the U.K. But perhaps the most ironic — or not — proposition was proffered on January 19, by the MIT Technology Review:

“An outbreak in the Western Hemisphere could give countries including the United States new reasons to try wiping out mosquitoes with genetic engineering.

“Yesterday, the Brazilian city of Piracicaba said it would expand the use of genetically modified mosquitoes …

“The GM mosquitoes were created by Oxitec, a British company recently purchased by Intrexon, a synthetic biology company based in Maryland. The company said it has released bugs in parts of Brazil and the Cayman Islands to battle dengue fever.”




Zika Freakout: The Hoax and the Covert Op Continue

 

Mosquito-Bite-Zika-Virus



If you want to hide anything on this planet, twist it into a (fake) story about a virus. You’re home free.

This is my second article on the Zika-virus scam (article archive here). I’ve been to these rodeos before: HIV, West Nile, Swine Flu, SARS, Ebola. In each case, a virus is blamed for illness and death that actually arises from other causes.

The Zika virus, now being blamed for the birth of babies with very small heads and impaired brains, has been around for a long time—late 1940s, early 1950s—and suddenly, without warning or reason, after inducing, at best, mild illness, it’s producing horrendous damage? This is called a clue. A clue that scientific liars are lying. Furthermore, many of the women who are giving birth to deformed babies test negative for the presence of the Zika Virus.

So, what is causing babies to be born with very small heads and brain damage? While researching my first book in 1987-8, AIDS INC., I concluded: don’t assume there is only one cause for illness. That can be very misleading. Various factors can combine to produce disease and death.

For example, in the case of this “Zika” phenomenon:

One: Pesticide use in Brazil:

 

Brazil, the center of the “Zika” crisis, uses more pesticides than any nation in the world. Some of these are banned in 22 other countries. And as for babies born with smaller heads, here is a study from Environmental Health Perspectives (July 1, 2011), “Urinary Biomarkers of Prenatal Atrazine Exposure…”:

“The presence versus absence of quantifiable levels of [the pesticide] atrazine or a specific atrazine metabolite was associated with fetal growth restriction… and small head circumference… Head circumference was also inversely associated with the presence of the herbicide metolachlor.” (emphasis added)

Atrazine and metolachlor are both used in Brazil.

Two: The TdaP vaccine:

 

This is a case of suspicious correlation. A study posted in the US National Library of Medicine, “Pertussis in young infants: a severe vaccine-preventable disease,” spells it out:

“…in late 2014, the [Brazilian] Ministry of Health announced the introduction of the Tdap vaccine for all pregnant women in Brazil.”

Obviously, pregnant women are the target group; they are giving birth to babies with smaller heads and brain damage, and the recommendation for them to take the vaccine was recent; 2014.

Barbara Loe Fisher, of the National Vaccine Information Center, writes:

“Drug companies did not test the safety and effectiveness of giving influenza or Tdap vaccine to pregnant women before the vaccines were licensed in the U.S and there is almost no data on inflammatory or other biological responses to these vaccines that could affect pregnancy and birth outcomes…The Food and Drug Administration (FDA) lists influenza and Tdap vaccines as either Pregnancy Category B or C biologicals which means that adequate testing has not been done in humans to demonstrate safety for pregnant women and it is not known whether the vaccines can cause fetal harm or affect reproduction capacity. The manufacturers of influenza and Tdap vaccines state that human toxicity and fertility studies are inadequate and warn that the influenza and Tdap vaccines should ‘be given to a pregnant woman only if clearly needed.’” (emphasis added)

Three: Genetically engineered mosquitoes that have already been released in Brazil to “combat” dengue fever—a project implemented by Oxitec, a company supplied with grant money from Bill Gates:

 

A town in Brazil has reported continuing elevated levels of dengue fever since the GE (genetically engineered) mosquitoes have been introduced to combat that disease.

The scientific hypothesis is: the trickster GE bugs (males) will impregnate natural females, but no actual next generation will occur beyond the larval stage. However, this plummeting birth rate in mosquitoes is the only “proof” that the grand experiment is safe. No long-term health studies have been done—this is a mirror of what happened when GMO crops were introduced: no science, just bland assurances.

Needless to say, without extensive lab testing, there is no way to tell what toxic elements these GE mosquitoes may actually be harboring, in addition to what researchers claim. That’s a major red flag.

Wherever these GE mosquitoes have been introduced, or are about to be introduced, the human populations have not been consulted for their permission. It’s all being done by government and corporate edict. It’s human experimentation on a grand scale.

Four: Pesticide manufacturing in Brazil:

 

Reuters, May 19, 2015, “Brazil prosecutors seek $16 million from pesticide makers”:

 “Brazilian prosecutors said on Monday they would seek at least 50 million reais ($16.6 million) from multinational pesticide manufacturers for alleged safety violations at a collection facility for used pesticide containers… Those manufacturers, prosecutors said, include the Brazilian units of BASF, DuPont, Monsanto, Nufarm, Syngenta, Adama, FMC and Nortox… The charges come as scientists, regulators, public health officials and consumers increasingly complain that Brazil’s ascent as an agricultural powerhouse has led to unsafe and excessive use of pesticides. Reuters reported in April that at least four foreign manufacturers sell pesticides in Brazil that they are not allowed to sell in their home markets.” (emphasis added)

How convenient for these corporate giants to evade blame for horrific birth effects—out of nowhere a virus is touted as the cause.

Five: Severe and endemic malnutrition, lack of basic sanitation, and grinding poverty:

 

These are major factors in all illness and death, in the areas where they are prevalent (e.g., major parts of Brazil). Suppression of the immune system is the result, and anything that then comes down the pipeline, germs or manmade toxic substances, become catastrophic to the body.

Six: anti-mosquito sprays:

 

The Guardian, January 26, 2015, “Brazil is ‘badly losing’ the battle against Zika virus, says health minister”:

Sprays are now being given out to 400,000 pregnant women in Brazil. Naturally, the sprays are toxic. What better way to multiply the attack on mothers and their unborn children? For example, widely used organophosphates in sprays can be highly disruptive to the nervous system.

Some or all of these six elements I’ve listed, in combination, form a sustained attack on human life.

And as I keep stressing, the virus becomes the formidable cover story that conceals the truth.

And don’t forget the Rio Olympic Games, coming up in August. There are multiple scenarios which could play out in front of a global television audience. Will Zika be pushed as some sort of worldwide pandemic? Will a Zika vaccine be magically “discovered” and rushed into production, in time to show (as an advertisement) lines of people dutifully trudging up to receive shots?

Every fake epidemic is, in part, designed to create fear and induce blind compliance to medical and government dictates. The germ is positioned as the “tiny terrorist” in this stage play.

In my first book, AIDS INC.(1988), I indicated that covert medical ops are the most dangerous, because they appear to be politically neutral, they fly under no flag, and they claim to forward only humanitarian aims. But in fact, modern “Rockefeller Medicine” is built as a vast partner in the Globalization of the planet. Its vision is a universal in-utero-to-cradle-to-grave system for the human race: every human walks a bleak lifelong path of disease-diagnosis after diagnosis, receiving toxic drugs and vaccines at every turn, which weaken his body and mind, and make him unable to consider what is happening outside his perimeter of suffering or resist political totalitarianism.

Medical freedom means: the freedom to refuse medical care, and it’s based on knowledge of destructive effects. This freedom must win, against any odds.

“Official science” is a contradiction in terms, and a grand illusion.


Thanks to reporters and researchers Jim Stone, Kathy Ford, the fullerton informer, Jim West, Martin Maloney, and Claus Jensen, who have moved this story forward and exposed the scam.

(To read about Jon’s mega-collection, Power Outside The Matrix, click here.) The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free NoMoreFakeNews emails here or his free OutsideTheRealityMachine emails here.





Zika and the New Climate Dystopia — Human Hothouse as Disease Multiplier

 

As of today, authorities in Brazil, Colombia, Jamaica, El Salvador and Venezuela were urging women to avoid getting pregnant… It is unthinkable. Or rather, it is something out of a science fiction story, the absolute core of a dystopian future.


There are a plethora of diseases out there. Diseases we don’t know about. Diseases locked away in far-off, rarefied corners of the world. Diseases that operate in small niche jungle environments. Diseases that live in only cave systems or within a single species. Diseases that were locked away millions of years ago in the now-thawing ice. Diseases that, if given a vector — or a means to travel outside of their little rarefied organic or environmental niches — can wreak untold harm across wide spans of the globe.


Countries with Reported Active Zika Transmission
(Countries with reported active Zika transmission. Until recently, Zika flare-ups had been isolated to Central Africa and French Polynesia. Now the virus is a global pandemic with World Health Organizations authorities concerned infections could top 4 million. Image source: The CDC.)


Such was the case with the once humble Zika virus. Discovered in 1947 in Central Africa, the disease first only existed in monkeys. The virus took 7 years to make the leap into humans in 1954. But, at first, symptoms were only mild and for most of the history of this disease it was considered to be a less harmful form of the Dengue Fever Virus — to which it is closely related. The virus, at first, appeared only to result in fever, headaches, rash and back pain — if any symptoms appeared at all. It would take much longer for the devastating and horrific after-effects of an, at first, seemingly harmless virus to begin to show up.

Until 2007, when the virus began to grow to its current pandemic levels, it was mostly isolated to Central Africa and a region of French Polynesia in the Pacific. Both areas are among the warmest and wettest in the world. Both featuring very large and persistent populations of the kinds of mosquitoes most suited for the transmission of this, now widely-feared, illness.


An Issue of The Expanding Range of Disease Vectors

In epidemiology parlance, a vector is a disease carrier. In the case of Zika, the primary carrier is the mosquito. In total, seven species of the Aedes variety of mosquitoes are known to carry Zika.

Under normal climate conditions, the ranges of these disease-bearing insects would tend to remain rather stable. But that’s not the case in the current world. Since 1880, the world has been warming and the extents of disease vector mosquitoes has been expanding. Under the current regime of 1 C temperature increase over the past 136 years, Aedes aegypti — one of the chief transporters of the Zika virus — has expanded its range on out of the tropics and into increasingly higher Latitudes.


Global_Aedes_aegypti_distribution
(Global Aedes aegypti distribution in 2015 — red indicates highest frequency, blue indicates zero frequency. Aedes aegypti is a disease vector for viruses like Dengue and Zika. As the globe has warmed, their range has been expanding into ever higher Latitudes. Image source: Aedes aegypti Distribution.)


But not only is the global extent of these disease carriers expanding — so is their persistence in the regions into which they’d previously occupied. Regions that may have seen only one or two weeks out of the year in which female, Zika infected, mosquitoes were active may now experience a month or two of exposure. And regions in which the mosquito was active for only a few months may now see active, disease-bearing populations for half of the year or more.

It is this increasing duration and expansiveness of disease vector exposure that is one of the most dangerous epidemiological impacts of climate change. Not only does climate change enable the movement of diseases out of previous isolation in remote reservoirs. It also enables an ever-broadening range of transport as the areas in which disease-carrying species are adapted to live dramatically expands both in terms of space and in terms of time of exposure.

It’s as if we decided to load up trillions of mosquitoes with what amounts to biological live rounds and then gave them the ability to unload that deadly ammunition over broader and broader expanses of the globe. That’s basically what you get when you warm the world. An expansion and global invasion of hitherto unknown illnesses spread throughout the world by vectors like the mosquito.


Zika’s Viral Explosion Occurs During Hottest Year on Record

Returning to our tale of the Zika virus’s expansion during 2007 through 2016, we find that Zika during this time-frame had leapt out of its traditional 20th Century range and expanded coincident with the spread of Aedes variety mosquitoes along the warming and moistening climate bands. In 2007, the first leap outside of Central Africa and French Polynesia occurred in Yap — a part of the Federated States of Micronesia.

The epidemic range then again expanded through 2014 into Easter Island, broader Polynesia, the Cook Islands, and New Caledonia. The geographic expansion of this illness along the Pacific Island chains indicates that Zika’s increased virility likely sparked from the French Polynesian strain and not from the strain in Africa.

Then, in 2015, coordinate with the hottest global temperatures on record, Zika leapt out of its Pacific Island basin environmental confines and spread into Brazil and the Caribbean. The virus subsequently spread through a broad section of Central and South America. As of yesterday, travel warnings of possible exposure to the Zika virus included this list of 22 countries:

Barbados, Bolivia, Brazil, Cape Verde, Colombia, Ecuador, El Salvador, French Guiana, Guadeloupe, Guatemala, Guyana, Haiti, Honduras, Martinique, Mexico, Panama, Paraguay, Puerto Rico, Saint Martin, Samoa, Suriname, and Venezuela.

By today,  the World Health Organization was issuing warnings that as many as 4 million people may end up being infected before the most recent outbreak is finished.


The New Climate Dystopia — We are Now Telling Women Not to Have Children

Like many viral fevers, Zika attacks the nervous systems of those it infects. And though initial onset symptoms may seem mild, with up to 80 percent of those infected showing no symptoms at all, the virus may cause severe longer-term damage to both the unborn and to vulnerable individuals. For as infection rates for the virus increased what were suspected to be related instances of a kind of temporary paralysis called Guillian Barre Syndrome and a terrifying shrinking of the heads of unborn infants called microcephaly also spiked.


Microcephaly 


(A spike in microcephaly rates — a tragic shrinking of the heads of unborn children as a result of viral damage to the nervous system — among infants in regions of Zika virus outbreak has raised global concerns about the virus’s ongoing impact. Most particularly, women in an expanding number of countries are now being asked to refrain from having children for months or even years. Image source: The CDC.)


From BBC today:

The virus, which has no symptoms 80% of the time, is blamed for causing stunted brain development in babies. About 3,500 cases of microcephaly have been identified in Brazil so far. And medical staff in Recife, a state capital in north-east Brazil, say they are struggling to cope with at least 240 cases of microcephaly in children.The city’s Health Secretary, Jailson Correia, a specialist in tropical diseases, told the BBC he and others needed “to fight very hard”.

These are profoundly terrible impacts. Ones that were not initially expected from a virus that at first seemed so innocuous. And it’s this threat of Zika-spawned microcephaly among infants that is spurring everything from travel warnings to the hitherto unprecedented measure of some countries requesting that their human populations take the extreme step of avoiding pregnancy.

As of Monday authorities in Brazil, Colombia, Jamaica, El Salvador and Venezuela were urging women not to get pregnant. The pregnancy moratorium — which is voluntary — ranges in duration from a few months to two years in the case of El Salvador. And the reason for the requested moratorium is sadly practical. Authorities in these countries are now forced to choose between asking women to avoid pregnancy or having their healthcare systems overwhelmed by infants suffering from microcephaly.

With a vaccine likely 10-12 years away for Zika, with 4 million cases expected in the current outbreak, and with the range of Aedes type mosquitoes who carry the virus continuing to expand on the back of a human-forced warming of the globe, we are sadly just at the beginning of this particular tragedy. An event that, as Bill McKibben noted in The Guardian earlier this week, has leapt fully into the realm of dystopia.


A Profound Dislocation For Humankind

Microcephaly among infants is both tragic and terrifying. Its impact strikes at the very heart of what it means to be a human being. If a virus, driven to far-flung regions by the heating of the world through fossil fuel burning, is able to cripple our children while still in the womb, our sense of security is shattered as we witness heart-breaking brutality. It’s the kind of thing so terrible it couldn’t come from the human imagination. Which is why, when we witness it, we experience a strange sense of dislocation. A surreal sense that all is not right. Like the moment after the car hit the telephone pole, the moment you’re still flying through the air flung free of the vehicle. The moment just before the inevitable impact with the pavement.

But the impact, sadly, does come. Not only are we turning many of the species of this world into climate orphans. Into creatures without a safe space in which to live and thrive, we are also doing it to ourselves. For the children of Zika are climate orphans too. The tragic victims of an expanding range of environmental conditions that are hazardous to human life. And Zika is but one example of the deadly diseases, extreme weather, sea level rise, glacial collapse, ocean death, and crop disruption we are now forcing upon the human habitat. A habitat we are rendering less livable for ourselves and pretty much everything else.

That’s what terminal dislocation means — to be forceably ejected. To be suddenly introduced into a very hostile environment in which survival, and in this case reproduction, is suddenly a crap shoot. For human beings, this is a profound dislocation. One that makes the world we’re living in now seem all-too-alien. For we’re not living in the world we are used to. And the one we’re making is both terrible and tragic. And, in all honesty, we desperately need to stop the damage before some other very big, or terrible, or essential thing breaks free.


Links:

The Zika Virus Foreshadows Our Climate Dystopian Future
About Climate Change and Vector-Borne Diseases
The CDC
The Zika Virus
Mosquito Borne Zika Virus Spreading Explosively
Aedes Aegypti
UCAR: Climate Change and Vector-Borne Disease
Brazilian City Sees Spike in Microcephaly Cases
Facts about Microcephaly
2 C Warming Increases Mosquito Population by 50 Percent




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