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Awareness The CDC’s Influenza Math Doesn’t Add Up: Exaggerating the Death Toll to Sell Flu Shots

By Robert F. Kennedy Jr. | Collective Evolution | October 10, 2018

Every year at about this time, public health officials and their media megaphones start up the drumbeat to encourage everyone (including half-year-old infants, pregnant women and the invalid elderly) to get a flu shot. Never mind that more often than not the vaccines don’t work, and sometimes even increase the risk of getting sick.

To buttress their alarmist message for 2018-2019, representatives from the Centers for Disease Control and Prevention (CDC) and other health agencies held a press conference and issued a press release on September 27, citing a particularly “record-breaking” (though unsubstantiated) 80,000 flu deaths last year. Having “medical experts and public health authorities publicly… state concern and alarm (and predict dire outcomes)” is part and parcel of the CDC’s documented playbook for “fostering public interest and high… demand” for flu shots. CDC’s media relations experts frankly admit that “framing” the current flu season as “more severe than last or past years” or more “deadly” is a highly effective strategy for garnering strong interest and attention from both the media and the public.

Peter Doshi (associate editor at The BMJ and a MIT graduate) has criticized the CDC’s “aggressive” promotion of flu shots, noting that although the annual public health campaigns deliver a “who-in-their-right-mind-could-possibly-disagree message,” the “rhetoric of science” trotted out each year by public health officials has a “shaky scientific basis.” Viewed within the context of Doshi’s remarks, the CDC’s high-flying flu numbers for 2017-2018 raise a number of questions. If accurate, 80,000 deaths would represent an enormous (and mystifying) one-year jump—tens of thousands more flu deaths compared to the already inflated numbers presented for 2016 (and every prior year). Moreover, assuming a roughly six-month season for peak flu activity, the 80,000 figure would translate to an average of over 13,300 deaths per month—something that no newspaper last year came close to reporting.

The CDC’s statistics are impervious to independent verification because they remain, thus far, unpublished—despite the agency’s pledge on its website to base its public health pronouncements on high-quality data derived openly and objectively. Could the CDC’s disappointment with influenza vaccination coverage—which lags far behind the agency’s target of 80%—have anything to do with the opacity of the flu data being used to peddle the unpopular and ineffective vaccines?

Fudging facts

There are a variety of reasons to question the precision with which the CDC likes to imbue its flu statistics. First, although the CDC states that it conducts influenza mortality surveillance with its partner agencies, there is no actual requirement for U.S. states to report adult flu deaths to the CDC. (In public health parlance, adult influenza deaths are not “reportable” or “nationally notifiable.”) In fact, the only “flu-associated deaths” that the CDC requires states and other jurisdictions to report are deaths in children—180 last year.

How did the CDC reach its as-yet-unpublished conclusion—widely shared with the media—that 79,820 American adults in addition to 180 children died from the flu in 2017-2018? The agency states that it relies on death certificate data. However, members of the Cochrane research community have observed that “when actual death certificates are tallied, influenza deaths on average are little more than 1,000 yearly.”

Other knowledgeable individuals have also noted that the death records system in the U.S. is subjective, incomplete and politicized, and have suggested that citizens should adopt a “healthy skepticism about even the most accepted, mainstream, nationally reported CDC or other ‘scientific’ statistics.” This skepticism may be especially warranted for the influenza stats, which are so inextricably intertwined with the CDC’s vaccination agenda that the statistical techniques and assumptions that the agency uses focus specifically on “project[ing] the burden of influenza that would have occurred in the absence of vaccination.”

Notwithstanding its incessant use of influenza statistics to justify its flu vaccine policies, the CDC tries to have it both ways, cautioning that because “influenza activity reporting… is voluntary,” influenza surveillance in the U.S. “cannot be used to ascertain how many people have become ill with influenza during the influenza season.” A larger problem is that the vital statistics that form the basis of the CDC’s surveillance data conflate deaths from pneumonia and influenza (P&I). The CDC concedes that this conflation complicates the challenge of specifically estimating flu deaths:

The system “tracks the proportion of death certificates processed that list pneumonia or influenza as the underlying or contributing cause of death. This system… does not provide an exact number of how many people died from flu” [emphasis added].

Curiously, the CDC presented its cause-of-death data slightly differently prior to 2015. Through 2014, the agency’s annual National Vital Statistics Reports included tables showing influenza deaths and pneumonia deaths as separate line items. Those reports made it abundantly clear that pneumonia deaths (at least as transmitted by death certificates) consistently and dramatically outstripped influenza deaths. The table below illustrates this pattern for 2012-2014.

Starting in 2015, the annual vital statistics reports began displaying P&I together and eliminated the distinct line items. At present, only one tool remains to examine mortality associated with influenza as distinct from pneumonia—the CDC’s interactive FluView dashboard—which provides weekly national breakdowns. The dashboard shows the same general pattern as in the annual reports—that is, lower numbers of influenza deaths and much higher numbers of pneumonia deaths. Bearing in mind all the shortcomings and potential biases of death certificate data, dashboard reports for the first week of March (week 9) for the past three years show 257 influenza deaths versus 4,250 pneumonia deaths in 2016, and 534 and 736 flu deaths (versus over 4,000 annual pneumonia deaths) in 2017 and 2018, respectively.

Semantic shenanigans

Semantics also play a key role in the CDC’s slippery communications about “flu.” For example, CDC’s outpatient surveillance focuses on the broad category of “influenza-like illness” (ILI)—an almost meaningless term describing general symptoms (fever, cough and/or sore throat) that any number of non-influenza viruses are equally capable of triggering. Cochrane lists several problems with the reliance on ILI to make inferences about influenza:

  • There is “no reliable system to monitor and quantify the epidemiology and impact of ILI” and no way of knowing what proportion of ILI is caused by influenza.
  • There are almost no reliable data on the number of ILI-related physician contacts or hospitalizations—and no one knows what proportion of ILI doctor visits and hospitalizations are due to influenza.

“Pneumonia,” too, is a catch-all diagnosis covering lung infections caused by a variety of different agents: viruses (non-influenza as well as influenza), bacteria, fungi, air pollutants and many others. Interestingly, hospitalization is a common route of exposure to pneumonia-causing pathogens, and mortality from hospital-acquired pneumonia exceeds 60%. In a plausible scenario, an adult hospitalized for suspected (but unconfirmed) “flu” could acquire a lethal pneumonia bug in the hospital, and their death might be chalked up to “flu” regardless of the actual facts, particularly because clinicians do not necessarily order influenza testing. When clinicians in outpatient settings do order testing, relatively few of the “flu” specimens—sometimes as low as 1%—actually test positive for influenza. Over the past couple of decades, the proportion of specimens testing positive has averaged around 15%—meaning that about 85% of suspected “flu” specimens are not, in fact, influenza.

Propaganda with a purpose

It takes little subtlety to recognize that the principal reason for flu hyperbole is to sell more vaccines. However, more and more people—even infectious disease specialists—are realizing that flu shots are fraught with problems. Roughly four-fifths of the vaccine injury and death cases settled through the National Vaccine Injury Compensation Program are flu-vaccine-related. A University of Toronto-based expert recently stated, “We have kind of hyped this vaccine so much for so long we are starting to believe our own hype.”

Pro-flu-vaccination studies—through their skillful placement in prestigious journals—tend to drown out other influenza studies that should be ringing warning bells. Published peer-reviewed studies show that:

  • Previous influenza vaccination, particularly in those who get a flu shot every year, diminishes or “blunts” the already low effectiveness of flu shots.
  • Getting vaccinated against influenza increases susceptibility to other severe respiratory viruses and also to other strains of influenza.
  • Mothers who receive influenza vaccines during pregnancy face an increased risk of miscarriages and their offspring face elevated risks of birth defects and autism.

A systematic review of influenza vaccine trials by Cochrane in 2010 urges the utmost caution. Noting that “studies funded from public sources [have been] significantly less likely [than industry-funded studies] to report conclusions favorable to the vaccines,” and citing evidence of “widespread manipulation of conclusions,” the Cochrane reviewers’ bottom line is that “reliable evidence on influenza vaccines is thin.” We should all keep those words in mind the next time the CDC and the media try to mischaracterize flu facts and science.

CHD is planning many strategies, including legal, in an effort to defend the health of our children and obtain justice for those already injured.  Your support is essential to CHD’s successful mission. Please visit our crowdfunding page.

October 11, 2018 Posted by | Deception, Science and Pseudo-Science | , | Leave a comment

Universal Vaccinations for Children will be Overseen by Committee which Accepts Vaccine Manufacturer Monies

By Janet Phelan – New Eastern Outlook – 10.12.2015

A House of Representatives Bill, short titled “Vaccinate All Children Act of 2015,” has been referred to the Subcommittee on Health and is awaiting committee action.

HR  2232 was introduced by Frederica Wilson, Democrat from Florida and is largely modeled on the California student vaccination act, which was signed into law by Governor Jerry Brown in June of this year.

Like the California Act, HR 2232 removes all previous exemptions from vaccination, other than a medical exemption, supported by a medical doctor’s statement that a particular vaccination would be hazardous to a specific child’s well- being. Gone are the religious exemptions and philosophical exemptions.

Previously, forty-eight states had laws on the books honoring religious exemptions and nineteen states allowed philosophical exemptions.

This Act would override any state law governing vaccine exemptions, making it mandatory for all students at public elementary and secondary schools to be vaccinated. The bill would amend the Public Health Services Act to require students “to be vaccinated in accordance with the recommendations of the Advisory Committee on Immunization Practices.” (ACIP)

The bill does not, however, reveal which vaccinations would be mandatory nor does it place a cap on vaccinations.

The above cited Advisory Committee, which will be making the decisions concerning which shots are mandatory, is stacked with pro-vaccination heavyweights. Notable committee members include a Dr. Kelly Moore, Director, Tennessee Immunization Program, Dr. Edward Belongia, Director, Center for Clinical Epidemiology & Population Health at the Marshfield Clinic Research Foundation  and Dr. Kathleen Harriman, Chief, Vaccine Preventable Disease Epidemiology Section with the California Department of Public Health, to name a few. Also sitting on the Committee as Ex Officio members are Department of Defense (DoD) officials as well as FDA officials and members of the Department of Veterans Affairs, among representatives from other federal agencies.

Dollars for Docs

A close scrutiny of this Advisory Committee reveals that quite a number of its members are enriching themselves through vaccine industry “donations” or grants.

For example, some of these individuals have a history which includes industry sponsorship or employment. An example is Dr. Belongia, who has been listed as Co-Principal Investigator for an industry sponsored study of effectiveness of quadrivalent influenza vaccine in children.

According to Propublica, a number of these vaccine experts on the Advisory Committee are accepting large sums of vaccine company money. Dr. Gregory Poland, who is with the American College of Physicians and also the Mayo Clinic, has received a total of $17,351.00 from vaccine manufacturers Novartis Vaccines and Sanofi Pasteur. The money changed hands, according to Propublica, for activities by Dr. Poland listed as promotional speaking, consulting and travel and food expenses from November 2013 through December 2014.

Dr. Stanley Grogg, a “Liaison Member” of the Committee and with American Osteopathic Association (AOA), was rewarded for his “promotional speaking” activities, as well as “consulting,” “travel and lodging” and of course the ubiquitous “food and beverage” — to the tune of  $60,391.00. These payments were made during the period of August 2013 through December 2014 and came from a buffet of pharmaceutical companies, including Pfizer, Sanofi, Novartis Vaccines and GlaxoSmithKline, among others.

Dr. Kenneth Schmader is listed as a “Liaison Member” of the ACIP, due to his position with the American Geriatrics Society (AGS). He is a Professor of Medicine-Geriatrics and Geriatrics Division Chief at Duke University and Durham VA Medical Centers in Durham, NC. Dr. Schmader received $75,913.79 for research, paid by Merck, Sharp and Dohme Corporation during the program year 2014.

Dr. Carol Baker, a “Liaison member” and with Infectious Diseases Society of America (IDSA) , also works as a Professor of Pediatrics with the Baylor College of Medicine in Houston, Texas. Dr. Baker was also found to have received $37,514.00 from August 2013-December 2014 for speaking, consulting, lodging and eating. The usual suspects pop up as the vaccine manufacturers who contributed to Dr. Baker—Novartis and Pfizer making the majority of the contributions.

Not to be left in the dust, Dr. William Schaffner, a “Liaison Member” from the National Foundation for Infectious Diseases (NFID) and the Chairman, Department of Preventive Medicine, Vanderbilt University School of Medicine, received a total payment of $26,208 in the two year period from Pfizer and Sanofi Pasteur. The total paid Dr. Schaffner for travel and lodging came to $13,653.00.

Committee member Dr. Ruth Karron, who is listed as  Professor and Director at the Center for Immunization Research, Department of International Health at Johns Hopkins Bloomberg School of Public Health in Baltimore, received $ $7,173 from GlaxoSmithKline for consulting from April-December, 2009, while Dr. Lee Harrison of Pittsburgh was paid a total of $27,663.00 by Glaxo and Pfizer, from 2009-2012.

Besides direct payments to pro- vaccine committee members from the pharmaceutical companies, there are other revenue streams gracing ACIP committee members. While this reporter did not find evidence that Advisory Committee member Dr. Arthur Reingold had received the above types of monies from Big Pharma, his name surfaced in connection with an effort to shut down a Professor whose work challenged the conventional wisdom that AIDS was mortally impacting large numbers of Africans. Reingold was assigned to “investigate” professor Peter Duesberg for “misconduct,” surrounding Duesberg’s findings that figures on AIDS deaths in Africa had been deliberately inflated.

As it turned out, Dr. Arthur Reingold had received over $37 million for AIDS research since 1988. Professor Duesberg was subsequently exonerated of the charges.

Dr. David Stephens, a voting member of the Committee, also did not show up on the Propublica list of doctors who took money from pharmaceutical companies. Stephens, whose bio states he has “led research initiatives in the School of Medicine” (at Emory University), is responsible for Emory researchers receiving “$521.8 million from eternal funding agencies in fiscal year 2014.” 

Stephens also hobnobs with the Vaccine Dinner Club, which exists to “advance the practice of vaccine science by stimulating the intellectual potential and research productivity of the vaccine research community in the Southeast…”

Dinners and membership in the club are free, sponsored by Emory University and other organizations. I guess with a half billion dollars knocking around in your pocket, a free lunch for your fellow scientists wouldn’t be much of an issue.

Stephens also sits on the Board of Directors for Georgia Bio, a non-profit organization dedicated to advancing the growth of Georgia’s life sciences industry. Also represented on the Georgia Bio Board are vaccine manufacturers and pharmaceutical companies: Johnson and Johnson, Geovax, Arbor Pharmaceuticals, Immucor, Osmotica Pharmaceutical Company and Femasys.

Georgia Bio was contacted by this reporter, who wished to query what, if any, compensation Stephens received for his service on the Board. Jennifer Kauffman, Development Director, promptly hung up rather than answer.

Should HR 2232 be approved by the US Congress, it is this Advisory Committee which will decide which vaccinations American children must receive. The clear conflict of interest inherent in Committee members padding their wallets with money from the pharmaceutical industry realistically should disqualify the members from making these critical decisions.

Opaque Government

These conflicts of interest are not new for the ACIP. As reported over fifteen years ago by the National Vaccine Information Center,  previous conflicts of interest ranged from  the ACIP chairman owning stock in vaccine giant Merck, to other financial ties between committee members and  vaccine companies. In addition, the National Vaccine Information Center reported that the mandated financial disclosures filed by committee members were incomplete, rendering a full accounting of their financial relationships with pharmaceutical companies difficult, if not impossible.

Regarding the compensation paid by the CDC to ACIP members, CDC reports that;“Appointments are not remunerated. However, members are compensated for expenses incurred by attendance at meetings. Such compensation, which includes the issuance of airline tickets, per diem to cover lodging, meals and incidental expenses will be in accordance with DHHS/CDC travel rules. An optional honorarium of $250/day for each day that a member attends an ACIP meeting is offered to voting members, who are designated as Special Government Employees during their tenure on the Committee.” 

Radio show host (Wise Women Media) Anita Stewart contributed research to this report. This reporter requested that Stewart contact the CDC to query what sort of compensation the ACIP members received, as the CDC will no longer respond to public records or media requests from this reporter. This blacklisting took place following the publication of an article in Activist Post, indicating that the CDC was deflating the numbers of biological weapons labs.

Stewart, who located the above information on ACIP compensation online, was questioned by CDC media officer Sonny Dill, who kept insisting that Stewart was I. Dill also wanted to know who Stewart worked for, stating this information was necessary before answering any questions. Stewart, who was forthcoming in response, reports that Dill declined to supply the information requested.

December 10, 2015 Posted by | Civil Liberties, Corruption, Deception, Science and Pseudo-Science | , , , , , , , , | Leave a comment

25 Facts About the Pharmaceutical Industry, Vaccines and “Anti-Vaxers”

By Julie Lévesque | Global Research | February 25, 2015

During the recent measles outbreak, the mainstream media blamed the epidemic solely on non vaccinated children, even though people who were vaccinated caught the disease and some vaccines have proven to be inefficient in the past. Without the slightest nuance, the mainstream media constantly portrays people reluctant to accept just any vaccine as “anti-vaxers”, irresponsible and misinformed people, relying on irrational fears and the one and only “fraudulent” Andrew Wakefield study linking autism to vaccines. (Watch Lina B. Moreco’s documentary Shots in the Dark, which features Dr. Wakefield and thankful parents of his young patients with autism.)

In reality, many so-called “anti-vaxers” are not ALL totally against vaccines. While some people may be totally against any kind of vaccination, many, including doctors and health specialists, question certain vaccines, ingredients in the vaccines and/or the vaccination schedule. This is not based on a survey but on my own perception resulting from the fair amount of articles on vaccines and the pharmaceutical industry that I’ve read over the last five years as a journalist. There are a large number of doctors and health specialists who have done truly independent research and who criticize vaccination based on scientific studies and solid evidence.

Why is the media so keen on portraying Big Pharma critics as crazy, uneducated, unscientific and irresponsible people?

Dr Marcia Angell worked for over two decades as editor of The New England Journal of Medicine.  She was fired after criticizing the pharmaceutical industry, which had exerted an overriding and negative influence on the scientific literature. She said:

“It is simply no longer possible to believe much of the clinical research that is published.”

Numerous journalists say the same goes for the mainstream media.

We bring to the attention of our readers 25 facts which constitute only part of a larger body of independent scientific research and articles on vaccines and the pharmaceutical industry. Some mainstream articles have been included as well to show how the media overlooks stories it has published in the past because they don’t fit with their “anti-vaxer” portrait.

The objective of this list is to provide independent research and sources of information on vaccination and Big Pharma, which is what the mainstream media fails to do and instead blindly promotes the narrative and agenda of Big Pharma.

(All emphasis added. Most titles are quotes from the articles they are linked to.)

25 Facts About the Pharmaceutical Industry, Vaccines and “Anti-Vaxers”

1- China has measles outbreaks but 99% are vaccinated

A recent study published in PLoS titled, “Difficulties in eliminating measles and controlling rubella and mumps: a cross-sectional study of a first measles and rubella vaccination and a second measles, mumps, and rubella vaccination,” has brought to light the glaring ineffectiveness of two measles vaccines (measles–rubella (MR) or measles–mumps–rubella(MMR) ) in fulfilling their widely claimed promise of preventing outbreaks in highly vaccine compliant populations. (Sayer Ji, Why Is China Having Measles Outbreaks When 99% Are Vaccinated?, GreenMedInfo 20 September 2014)

2- Mandatory Chickenpox Vaccination Increases Disease Rates, Study Shows

Varicella, or the chicken pox vaccination, has been mandated in South Korea since 2005. Infants from 12 to 15 months are required by law to receive a vaccination. By 2011, the country reached a near universal compliance rate, however, varicella patients did not decrease; they have increased since reaching this mandated level of vaccination.

The number of chicken pox patients reported to the Korea Centers for Disease Control and Prevention (KCDC) has increased from 22.6 cases per 100,000 in 2006 to 71.6 cases per 100,000 in 2011.  That’s a huge difference and ample proof that the vaccination program isn’t working to control the spread of the disease. (Christina Sarich, With 97% Compliance Chicken Pox Vaccine Still Causes Outbreaks, Natural Society, January 08, 2015)

3- In a 2012 measles outbreak in Quebec (Canada) over half of the cases were in vaccinated teenagers

An investigation into an outbreak in a high school in a town that was heavily hit by the virus found that about half of the cases were in teens who had received the recommended two doses of vaccine in childhood — in other words, teens whom authorities would have expected to have been protected from the measles virus.

It’s generally assumed that the measles vaccine, when given in a two-dose schedule in early childhood, should protect against measles infection about 99 per cent of the time. So the discovery that 52 of the 98 teens who caught measles were fully vaccinated came as a shock to the researchers who conducted the investigation. (The Canadian Press, Measles among vaccinated Quebec kids questioned, CBC, October 20, 2011)

4- In 1987 a measles outbreak was documented among a fully immunized group of children

In 1987, for example, a study published in the New England Journal of Medicine (NEJM) documented a measles outbreak that occurred in Corpus Christi, Texas, in the spring of 1985. Fourteen adolescent-age students, all of whom had been vaccinated for measles, contracted the disease despite having been injected with the MMR vaccine. Researchers noted that more than 99 percent of students at the school — basically all of them — had also been vaccinated, with more than 95 percent of them showing detectable antibodies to measles. (Ethan A. Huff, Measles Outbreak Documented Among Fully Immunized Group of Children, Natural News 15 February 2015)

5- Centers for Disease Control’s (CDC) Own Data Shows Links Between Vaccines and Sudden Infant Death Syndrome (SIDS)

What happens when the actual evidence from the scientific and clinical literature produced by these very agencies contradicts their own vaccine policies?

This is exactly what has happened with the publication of a new study in the Journal of Pediatrics titled ,”Adverse Events following Haemophilus influenzae Type b Vaccines in the Vaccine Adverse Event ReportingSystem, 1990-2013,” wherein CDC and FDA researchers identify 749 deaths linked to the administration of the Hib vaccine, 51% of which were sudden infant death linked to the administration of Hib vaccine. (Sayer Ji, Centers for Disease Control’s (CDC) Own Data Shows Links Between Vaccines and Sudden Infant Death Syndrome (SIDS), GreenMedInfo 23 January 2015)

6- Japan banned the MMR vaccine in 1993 “after 1.8 million children had been given two types of MMR and a record number developed non-viral meningitis and other adverse reactions.”

The Japanese government realised there was a problem with MMR soon after its introduction in April 1989 when vaccination was compulsory. Parents who refused had to pay a small fine.

An analysis of vaccinations over a three-month period showed one in every 900 children was experiencing problems. This was over 2,000 times higher than the expected rate of one child in every 100,000 to 200,000. (Jenny Hope, Why Japan banned MMR vaccine, Daily Mail)

7- A study concluded nations that require more vaccine doses tend to have higher infant mortality rates.

The US childhood immunization schedule requires 26 vaccine doses for infants aged less than 1 year, the most in the world, yet 33 nations have better IMRs [Infant Mortality Rates]

Some countries have IMRs that are less than half the US rate: Singapore, Sweden, and Japan are below 2.80. According to the Centers for Disease Control and Prevention (CDC), “The relative position of the United States in comparison to countries with the lowest infant mortality rates appears to be worsening.”

These findings demonstrate a counter-intuitive relationship: nations that require more vaccine doses tend to have higher infant mortality rates. (Neil Z Miller and Gary S Goldman, Infant mortality rates regressed against number of vaccine doses routinely given: Is there a biochemical or synergistic toxicity?,  U.S. National Library of Medicine, September 2011)

8- The U.S. has a vaccine court apparently designed to “Shield Manufacturers from Liability”

For years, the corporate media was reluctant to admit that it even existed. But the special court system designed to handle vaccine injury cases — and ultimately sweep them under the rug as quickly as possible — has hit the mainstream news for its failure to adequately and propitiously compensate families of vaccine-injured children. (Ethan A. Huff, Secretive Vaccine Court Exposed: Designed to Shield Manufacturers from Liability, Natural News, November 19, 2014)

9- Beyond admitting to fraud in a 2004 Centers for Disease Control (CDC) study that exonerated the MMR vaccine, Dr. William Thompson, a CDC scientist, asserts there is a connection between mercury (thimerosal) in vaccines and autism. (Jon Rappoport, U.S. Centers for Disease Control Whistleblower: Mercury (Thimerosal) in Vaccines Causes Autism, No More Fake News, September 05, 2014)

10- Back in 2002, William Thompson was already aware of study results linking the MMR vaccine to a very large increase in autism risk among African-American children. See Brian Hooker’s published paper here, with a full analysis of the CDC’s own data revealing a 340% increased risk of autism in African-American children following the MMR vaccine. (Mike Adams, Autism Links to Vaccines: Whistleblower Reveals Evidence of Criminal Coverup by the Centers for Disease Control (CDC), Natural News August 26, 2014

11- According to a CDC epidemiologist named Tom Verstraeten, who had analyzed the agency’s massive database containing the medical records of 100,000 children, a mercury-based preservative in the vaccines — thimerosal — appeared to be responsible for a dramatic increase in autism and a host of other neurological disorders among children. (Robert F. Kennedy Jr, Vaccinations: Deadly Immunity. Government Cover-up of a Mercury / Autism Scandal Rollingstone.com, 20 July 2005)

12- Instead of taking immediate steps to alert the public and rid the vaccine supply of thimerosal, the officials and executives [discussed] how to cover up the damaging data. (Ibid.)

The CDC paid the Institute of Medicine to conduct a new study to whitewash the risks of thimerosal, ordering researchers to “rule out” the chemical’s link to autism.

It withheld Verstraeten’s findings, even though they had been slated for immediate publication, and told other scientists that his original data had been “lost” and could not be replicated. And to thwart the Freedom of Information Act, it handed its giant database of vaccine records over to a private company, declaring it off-limits to researchers. By the time Verstraeten finally published his study in 2003, he had gone to work for GlaxoSmithKline and reworked his data to bury the link between thimerosal and autism.

11- Since 1991, when the CDC and the FDA had recommended that three additional vaccines laced with the preservative be given to extremely young infants […] the estimated number of cases of autism had increased fifteenfold [in 2005], from one in every 2,500 children to one in 166 children.(Ibid.)

Here is the CDC chart available today on its website:

An MIT researcher has linked autism to glyphosate, the chemical herbicide used in Monsanto Roundup.

12- Vaccine manufacturers […] continued to sell off their mercury-based supplies of vaccines until last year [2004].

The CDC and FDA [bought] up the tainted vaccines for export to developing countries and allowed drug companies to continue using the preservative in some American vaccines — including several pediatric flu shots as well as tetanus boosters routinely given to eleven-year-olds. (Ibid.)

13- Senate Majority Leader Bill Frist, who has received $873,000 in contributions from the pharmaceutical industry, has been working to immunize vaccine makers from liability in 4,200 lawsuits that have been filed by the parents of injured children. (Ibid.)

14- Seasonal Flu Shots still contain thimerosal.

Look at the monographs. For example the one from Vaxigrip from Sanofi Pasteur states on page 4 the mercury-based preservative is in its multidose vial:

“Clinically Relevant Non-medicinal Ingredients: thimerosal* , formaldehyde, Triton® X-100†, neomycin”

15- Dr. Scott Reuben former member of Pfizer’s speakers’ bureau published dozens of fake study in medical journals

Dr. Reuben accepted a $75,000 grant from Pfizer to study Celebrex in 2005… His research, which was published in a medical journal, has since been quoted by hundreds of other doctors and researchers as “proof” that Celebrex helped reduce pain during post-surgical recovery. .. No patients were ever enrolled in the study!

He also faked study data on Bextra and Vioxx drugs… [T]he peer-reviewed medical journal Anesthesia & Analgesia was forced to retract 10 “scientific” papers authored by Reuben… 21 articles written by Dr. Reuben that appear in medical journals have apparently been fabricated, too, and must be retracted. (Big Pharma researcher admits to faking dozens of research studies for Pfizer, Merck (opinion), Mike Adams,  NaturalNews.com, February 18, 2010)

16- To this day thimerosal is still used in flu vaccines

For example, in the Vaxigrip monograph says: “The multidose vial of this vaccine contains thimerosal as a preservative. Thimerosal has been associated with allergic reactions.”

17- There are at least 97 studies showing links between vaccines and autism.

18- The CDC claims “there is no convincing evidence of harm caused by the low doses of thimerosal in vaccines”, but that health authorities “agreed that thimerosal should be reduced or eliminated in vaccines as a precautionary measure.”

On thimerosal, the CDC website states:

“Since 2001, with the exception of some influenza (flu) vaccines, thimerosal is not used as a preservative in routinely recommended childhood vaccines. Thimerosal is a mercury-containing preservative used in some vaccines and other products since the 1930′s. except for minor reactions like redness and swelling at the injection site. However, in July 1999, the Public Health Service agencies, the American Academy of Pediatrics, and vaccine manufacturers agreed that thimerosal should be reduced or eliminated in vaccines as a precautionary measure.“

19- Industry-sponsored trials published in medical journals consistently favor sponsors 

In view of this control and the conflicts of interest that permeate the enterprise, it is not surprising that industry-sponsored trials published in medical journals consistently favor sponsors —largely because negative results are not published, positive results are repeatedly published in slightly different forms, and a positive spin is put on even negative results. A review of seventy-four clinical trials of antidepressants, for example, found that thirty-seven of thirty-eight positive studies were published. But of the thirty-six negative studies, thirty-three were either not published or published in a form that conveyed a positive outcome.” – Marcia Angell, MD (Dr. Gary G. Kohls, Beware the Drug Companies, How they Deceive Us: “Criticizing Big Pharma” Global Research, February 16, 2015)

20- Nearly half of published articles in scientific journals contain findings that are false. (Dr. Gary G. Kohls, Beware the Drug Companies, How they Deceive Us: “Criticizing Big Pharma”Global Research, February 16, 2015)

“Six years ago, John Ioannidis, a professor of epidemiology at the University of Ioannina School of Medicine in Greece, found that nearly half of published articles in scientific journals contained findings that were false, in the sense that independent researchers couldn’t replicate them. The problem is particularly widespread in medical research, where peer-reviewed articles in medical journals can be crucial in influencing multimillion- and sometimes multibillion-dollar spending decisions. It would be surprising if conflicts of interest did not sometimes compromise editorial neutrality, and in the case of medical research, the sources of bias are obvious.

21- Most medical journals receive half or more of their income from pharmaceutical company advertising and reprint orders, and dozens of others [journals] are owned by companies like Wolters Kluwer, a medical publisher that also provides marketing services to the pharmaceutical industry.” — Helen Epstein, author of “Flu Warning: Beware the Drug Companies” (http://aaci-india.org/COI/Flu_web_final.pdf) (Dr. Gary G. Kohls, Beware the Drug Companies, How they Deceive Us: “Criticizing Big Pharma” Global Research, February 16, 2015)

22- The FDA’s own web page admits that the drugs it certifies as safe contribute to over 100,000 deaths per year. (Constitutional Attorney on US Federal Drug Administration (FDA) Corruption, Disinformation and Cover Up of Health Dangers, Activist Post,  8 February 2015)

23- The FDA routinely approves drugs over objections from its own medical reviewers. (Ibid.)

24- The FDA does zero independent medical testing of its own.

It is a system built upon conflicts of interest that leaves consumers completely in the dark about the true consequences of taking Big Pharma products. (Ibid.)

25- In 2012 GlaxoSmithKline Pleaded Guilty and Paid “$3 Billion to Resolve Fraud Allegations and Failure to Report Safety Data”

According to the US Justice Department:

The resolution is the largest health care fraud settlement in U.S. history and the largest payment ever by a drug company. …

GSK agreed to plead guilty to a three-count criminal information, including two counts of introducing misbranded drugs, Paxil and Wellbutrin, into interstate commerce and one count of failing to report safety data about the drug Avandia to the Food and Drug Administration (FDA).

March 29, 2015 Posted by | Mainstream Media, Warmongering, Science and Pseudo-Science | , | Leave a comment

Drug-Induced Dementia isn’t Alzheimer’s

By Dr. Gary G. Kohls | Global Research | February 26, 2015

“More than 50 conditions can cause or mimic the symptoms of dementia.” and “Alzheimer’s (can only be) distinguished from other dementias at autopsy.” – from a Harvard University Health Publication entitled What’s Causing Your Memory Loss? It Isn’t Necessarily Alzheimer’s

“Medications have now emerged as a major cause of mitochondrial damage, which may explain many adverse effects. All classes of psychotropic drugs have been documented to damage mitochondria, as have statin medications, analgesics such as acetaminophen, and many others.” – Neustadt and  Pieczenik, authors of Medication-induced Mitochondrial Damage and Disease

“Establishing mitochondrial toxicity is not an FDA requirement for drug approval, so there is no real way of knowing which agents are truly toxic.”  – Dr. Katherine Sims, Mass General Hospital –http://www.mitoaction.org

“It is difficult to get a man to understand  something, when his salary depends upon his not understanding it!” – Upton Sinclair, anti-fascist, anti-imperialist American author who wrote in the early 20thcentury

“No vaccine manufacturer shall be liable… for damages arising from a vaccine-related injury or death.” – President Ronald Reagan, as he signed The National Childhood Vaccine Injury Act (NCVIA) of 1986, absolving drug companies from all medico-legal liability when children die or are disabled from vaccine injuries.

Over the past several decades there have been a number of well-financed campaigns, promoted by well-meaning laypersons, to raise public awareness to the plight of patients with dementia. Suspiciously, most of these campaigns that come from “patient support” groups lead the public to believe that every dementia patient has Alzheimer’s dementia (AD).

Not so curiously, it turns out that many – perhaps all – of these campaigns have been funded – usually secretly – by the very pharmaceutical companies that benefit economically by indirectly promoting the sale of so-called Alzheimer’s drugs. Such corporate-generated public relations “campaigns” are standard operating procedure for all of BigPharma drugs, especially its psychopharmaceutical drugs. BigPharma has found that the promotion and de-stigmatization of so-called “mental illnesses” (for which there are FDA-approved drugs) is a great tool for marketing their drugs.

Recently Alzheimer’s support groups all around the nation have been sponsoring the documentary about country singer Glen Campbell who has recently been diagnosed by his physicians with Alzheimer’s disease (of unknown etiology) despite the obvious fact that Campbell was infamous for his chronic heavy use of brain-damaging, dementia-inducing, addicting, and very neurotoxic drugs like cocaine and alcohol. And, just like so many other hard-living celebrities like the recently suicidal Robin Williams, Campbell was known to have received prescriptions of legal drugs from their prescribing boutique psychiatrists and physicians, just adding to the burden that their failing livers, brains and psyches had to endure.

Since it is known that Alzheimer’s disease can only be truly diagnosed by a microscopic examination of the cerebral cortex (at autopsy), we have to question the very alive Glen Campbell’s diagnosis. And we also have to question the veracity and motivations of the sponsoring patient support groups and their BigPharma sponsors.

Is the Alzheimer’s Epidemic Actually a Drug-Induced Dementia Epidemic?

Synchronous with the huge increases (over the past generation or so) in

1) the incidence of childhood and adult vaccinations,

2) the widespread use of psychotropic and statin (cholesterol-lowering) drug use, and

3) the increased ingestion of a variety of neurotoxic substances – including food additives, there has been a large parallel increase in the incidence of

a) chronic illnesses of childhood, including autistic spectrum disorders,

b) “mental illnesses of unknown origin”, and also

c) dementia, a multifactorial reality which, via clever marketing and the studied ignorance of what is scientifically known about the actual causes – and diagnosis – of dementia, which has been primarily – and mistakenly – referred to as Alzheimer’s disease (of unknown etiology).

It is important to ask and then demand an honest answer to the question “could there be a connection between America’s increasingly common over-prescribing of immunotoxic, neurotoxic, synthetic prescription drugs and vaccines and some of the neurodegenerative disorders that supposedly “have no known cause”?

Could the economically disabling American epidemic of autoimmune disorders, psychiatric disorders, autism spectrum disorders, etc (all supposedly of unknown origin) that have erupted over the past several decades be found to have recognizable root causes and therefore be treatable and, most importantly, preventable?

These are extremely important questions, especially in the case of the current dementia epidemic, because the so-called Alzheimer’s patient support groups seem to be totally unaware of the powerful evidence that prescription drugs known to damage brain cells (especially by poisoning their mitochondria) would be expected to cause a variety of neurological and psychological disorders because of the brain cell death that eventually happens when enough of the mitochondria (the microscopic hearts and lungs of every cell) have been wounded irretrievably or killed off. (See more info on drugs and mitochondria below.)

One of the big problems in America’s corporate-controlled culture, corporate-controlled media and corporate-controlled medical industries is that the giant pharmaceutical corporations, who are in the business of developing, marketing and selling known mitochondrial toxins (in the form of their drugs and vaccine ingredients) have a special interest in pretending that there is no known cause for the disorders that their synthetic chemicals are causing (or they use the unprovable “it’s probably genetic” subterfuge).

It should be a concern of everybody who knows a demented patient, that some AD patient support groups are known to be front groups for the pharmaceutical companies that profit from the marketing to patients and their doctors the disappointingly ineffective drugs for Alzheimer’s like Aricept, Exelon, Namenda, Hexalon, and Razadyne.

Prescription Drug-Induced – and Vaccine-Induced – Mitochondrial Disorders

Acquired mitochondrial disorders (as opposed to the relatively rare primary mitochondrial disorders like muscular dystrophy) that can be caused by commonly prescribed drugs are difficult to diagnose and are generally poorly understood by most practitioners. When I went to med school, nobody knew anything about what synthetic drugs or vaccines did to the mitochondria.

A lot of mitochondrial research, especially since the 1990s, has proven the connections between a variety of commonly prescribed medications and mitochondrial disorders. That evidence seems to have been cunningly covered-up by the for-profit pharma groups (who control medical education and much of the media) and various other powers-that-be because of the serious economic consequences if the information was allowed in the popular press. The stake-holders in the pharmaceutical and medical industries, most of whom profit mightily from the routine and increasing usage of neurotoxic drugs and vaccines, supposedly operating in the name of Hippocrates, would be very displeased if this information got out. I submit that BigPharma’s cover-up of the connections is totally unethical and, in the opinion of many other whistleblowers, criminal.

An Honest Patient Guide for Dementia Patients from Harvard!

So I was pleasantly surprised to find a reasonably honest guide for dementia patients on a Harvard University website.

(The entire guide can be accessed at http://www.helpguide.org/harvard/whats-causing-your-memory-loss.htm#top.)

The information at that website stated that there were over 50 conditions that could cause or mimic early dementia symptoms. I hadn’t been taught anything about that reality when I went to med school, and I doubt that many of my physician colleagues were either. And besides, what medical practitioner in our double-booked clinic environment, even if he or she was aware, has the time to thoroughly rule out the 50 conditions when confronted with a patient with memory loss?

I have often said to my patients and my seminar participants: “it takes only 2 minutes to write a prescription, but it takes 20 minutes to not write a prescription”. And in the current for-profit clinic culture, time is money and few physicians are given the “luxury” of spending adequate time with their patients. (In defense of the physicians that I know, they are not happy about that reality but don’t know what to do about it.)

It is so tempting to use the popularized, but rather squishy label of AD (of unknown etiology) rather than to educate ourselves about the possibility of drug- or vaccine-induced dementia. But what is so important is that many of the 50+ conditions are preventable or reversible, which will be therapeutic only if the conditions are identified before permanent brain damage occurs.

The Harvard guide actually said that “medications are common culprits in mental decline. With aging, the liver becomes less efficient at metabolizing drugs, and the kidneys eliminate them from the body more slowly. As a result, drugs tend to accumulate in the body. Elderly people in poor health and those taking several different medications are especially vulnerable.”

The guide continued with a list of the possible classes of prescription drugs that number in the hundreds:

 “The list of drugs that can cause dementia-like symptoms is long. It includes antidepressants, antihistamines, anti-Parkinson drugs, anti-anxiety medications, cardiovascular drugs, anticonvulsants, corticosteroids, narcotics, sedatives.”

The Harvard guide went on to emphasize that Alzheimer’s can only be accurately diagnosed on a post-mortem examination. The guide states that “Alzheimer’s is distinguished from other dementias at autopsy by the presence of sticky beta-amyloid plaques outside brain cells (neurons) and fibrillary tangles within neurons (all indicative of cellular death). Although such lesions may be present in any aging brain, in people with Alzheimer’s these lesions tend to be more numerous and accumulate in areas of the brain involved in learning and memory.”

“The leading theory is that the damage to the brain results from inflammation and other biological changes that cause synaptic loss and malfunction, disrupting communication between brain cells. Eventually the brain cells die, causing tissue loss In imaging scans, brain shrinkage is usually first noticeable in the hippocampus, which plays a central role in memory function.”

But even the Harvard guide inexplicably failed to mention known mitochondrial toxins such as statin drugs, metformin, Depakote, general anesthetics, fluoroquinolone antibiotics, fluorinated psychotropic drugs, NutraSweet (every molecule of aspartame, when it reaches 86 degrees F, releases one molecule of the excitotoxin aspartic acid and one molecule of methanol [wood alcohol] which metabolizes into the known mitochondrial poison formaldehyde [embalming fluid]), pesticides (including the chlorinated artificial sweetener Splenda, which was initially developed as a pesticide) or the mercury (thimerosal), aluminum and formaldehyde which are common ingredients in vaccines. These are only some of the synthetic drugs that are capable of causing mitochondrial damage in brain cells – with memory loss, confusion and cognitive dysfunction, all early symptoms of dementia.

It is tragic, but all–too-common, for reversible and preventable drug-induced dementias (therefore of known cause and thus not Alzheimer’s) to be mis-diagnosed as Alzheimer’s disease “of unknown etiology” and to then be prescribed costly, essentially ineffective and potentially toxic drugs – whose mitochondrial toxicities have not been tested for.

(The pharmaceutical industry, it should be noted, is not required by the FDA to test its drugs for mitochondrial toxicity when it is doing its studies for marketing approval, again exhibiting the total disdain for the Precautionary Principle by both industry and the regulatory agencies such as the FDA, the CDC and WHO.)

There is much more in the basic neuroscience literature proving the connections, at least from authors who do not have conflicts of interest with BigPharma and BigMedicine. The authors of these articles have raised the questions and have published the proof that concerned families of patients and their physicians desperately need to know.

Don’t expect BigPharma to respond or to offer apologies or mea culpas. Do expect denials, dismissals, distractions, discrediting and then the delaying of real legitimate explorations of the real scientific evidence that exposes its subterfuge in the name of maintaining large profits for their stakeholders.

Here are the abstracts from just two of the many peer-reviewed articles from various science journals that support the thesis of this column.

Medication-induced mitochondrial damage and disease

Published in the Molecular Nutrition and Food Research journal ; 2008 Jul;52(7):780-8.

Authors: Neustadt, J,  Pieczenik SR.

Abstract

Since the first mitochondrial dysfunction was described in the 1960s, the medicine has advanced in its understanding the role mitochondria play in health and disease. Damage to mitochondria is now understood to play a role in the pathogenesis of a wide range of seemingly unrelated disorders such as schizophrenia, bipolar disease, dementia, Alzheimer’s disease, epilepsy, migraine headaches, strokes, neuropathic pain, Parkinson’s disease, ataxia, transient ischemic attack, cardiomyopathy, coronary artery disease, chronic fatigue syndrome, fibromyalgia, retinitis pigmentosa, diabetes, hepatitis C, and primary biliary cirrhosis. Medications have now emerged as a major cause of mitochondrial damage, which may explain many adverse effects. All classes of psychotropic drugs have been documented to damage mitochondria, as have statin medications, analgesics such as acetaminophen, and many others. While targeted nutrient therapies using antioxidants or their precursors (e. g., N-acetylcysteine) hold promise for improving mitochondrial function, there are large gaps in our knowledge. The most rational approach is to understand the mechanisms underlying mitochondrial damage for specific medications and attempt to counteract their deleterious effects with nutritional therapies. This article reviews our basic understanding of how mitochondria function and how medications damage mitochondria to create their occasionally fatal adverse effects.

Mitochondrial Dysfunction and Psychiatric Disorders

From: The Journal of Neurochemical Research 2009 Jun;34(6):1021-9.

Abstract

Mitochondrial oxidative phosphorylation is the major ATP-producing pathway, which supplies more than 95% of the total energy requirement in the cells. Damage to the mitochondrial electron transport chain has been suggested to be an important factor in the pathogenesis of a range of psychiatric disorders. Tissues with high energy demands, such as the brain, contain a large number of mitochondria, being therefore more susceptible to reduction of the aerobic metabolism. Mitochondrial dysfunction results from alterations in biochemical cascade and the damage to the mitochondrial electron transport chain has been suggested to be an important factor in the pathogenesis of a range of (so-called) neuropsychiatric disorders, such as (psychotropic drug-treated) bipolar disorder, depression and schizophrenia….Alterations of mitochondrial oxidative phosphorylation in (anti-psychotic drug-treated) schizophrenia have been reported in several brain regions and also in platelets. Abnormal mitochondrial morphology, size and density have all been reported in the brains of (anti-psychotic drug-treated) schizophrenic individuals. Considering that several studies link energy impairment to neuronal death, neurodegeneration and disease, this review article discusses energy impairment as a mechanism underlying the pathophysiology of some psychiatric disorders, like (psychotropic drug-treated) bipolar disorder, depression and schizophrenia.

Dr Kohls is a retired physician who practiced holistic mental health care for the last decade of his career, and took seriously the Hippocratic Oath that he swore when he received his medical degree. He is also a peace and justice advocate and writes a weekly column for the Reader Weekly, an alternative newsweekly published in Duluth, Minnesota, USA. The last three years of Dr Kohls’ columns are archived at http://duluthreader.com/articles/categories/200_Duty_to_Warn.

February 26, 2015 Posted by | Deception, Science and Pseudo-Science | , , , , , , , , , , , , , | Leave a comment

Why Does the American Academy of Pediatrics Put Corporate Profits Ahead of Children’s Health?

By GARY NULL AND RICHARD GALE | CounterPunch | December 22, 2012

The United Nations recently announced that its Fifth Intergovernmental Negotiating Committee session, scheduled for January 2013, would propose a binding treaty to ban ethylmercury (commonly known as thimerosal) from all medications and vaccines worldwide. That is welcome news. But it has laid bare the battle lines between those government health departments and professional medical organizations who value the health of children and those who favor drug profiteering.

It is no surprise that the pharmaceutical industry and its special interest groups are moving aggressively to oppose a UN treaty ban on mercury. After all, one of Big Pharma’s prime directives is to resist any legislation, domestic or international, that threatens its sales and revenues.  But it is a big surprise, indeed, that the American Academy of Pediatrics (AAP)—once a leader in advocating the removal of mercury from all medical products and vaccines—would now suddenly hold hands with Big Pharma to oppose the UN’s proposal.

Why would the AAP join with Big Pharma to oppose the UN mercury ban?  Why would it back-pedal away from its earlier confirmation that vaccine mercury is toxic and poses serious health risks? A look at the history of the AAP’s position on mercury will show us why. In its July 2001 issue of Pediatrics, the AAP released its official position on mercury: “Mercury in all its forms is toxic to the fetus and children, and efforts should be made to reduce exposure to the extent possible to pregnant women and children as well as the general population.”[1]  Yet in the recent December 17 2012 issue of Pediatrics, former AAP president Louis Cooper writes, “Science clearly documented that we can’t find hazards from thimerosal in vaccines… The preservative plays a critical role in distribution of vaccine to the global community. It was a no-brainer what our position needed to be.”[2]

The AAP’s original warning against thimerosal arrived a year following the illegal secret meeting convened by the CDC at the Simpsonwood retreat center near the CDC’s headquarters in Atlanta. At that meeting, federal and international health officials, executives from the vaccine industry, and members of professional medical associations, including the AAP, were informed about the CDC’s analysis of vaccine injury reports in its Vaccine Safety Database (VSD). The study, known as the Verstraeten study after the name of its chief investigator, concluded that there was a direct link between vaccine mercury and the rise in autism. In a letter published in the journal Pediatrics, Dr. Eric Coleman at the FDA wrote, “the fact is, no preclinical or clinical studies were ever conducted to specifically examine the safety of thimerosal at the doses found when used in multiple infant and childhood vaccines. Thus, there is no conclusive evidence because there were no studies.”[3]

The Verstraeten study also led to Congressional hearings. The CDC was reprimanded for negligence, careless scientific oversight, conflicts of interest with the pharmaceutical industry and administrative incompetence regarding decisions to protect children’s health.  Eventually policies were enforced to remove thimerosal from vaccines given in the US; although this mandate was never carried out thoroughly to this day.

However, thimerosal reduction and removal only applied to vaccines distributed in the US. Vaccine makers continued to manufacture vaccines containing thimerosal to other countries, particularly in the developing world. American stockpiles of mercury containing vaccines were simply sold and exported overseas.

During a period of several years the CDC further manipulated, massaged, and distorted the original Verstraeten research to hide any data that would suggest possible causality between mercury and autistic disorders. On five separate occasions Dr. Verstraeten slanted data. For example, 25% of reported vaccine injuries were cherry picked and removed to generate statistical confusion. The CDC’s final paper was published in the AAP’s Pediatrics journal and declared vaccine thimerosal safe and does not contribute to neurological damage in infants and children. As a side note, Dr. Verstraeten had already slipped out of the CDC to work for GlaxoSmithKline’s vaccine division when his paper was published.

The CDC’s publication in Pediatrics completely altered how vaccines would be manufactured for American children and resurrected the thimerosal-autism debate. But more important it is among the greatest scientific perversions in the history of medical literature.  The AAP was complicit in the fraud for having failed to conduct due diligence and proper peer-review before approving it for publication. Instead the Academy sided with Big Pharma’s favorite lobbying group—the CDC.

The story of the secret Simpsonwood meeting, the CDC’s subsequent fraudulent studies, Congressional investigations and the National Institute of Environmental Health Science’s analysis of the CDD’s research is well documented. However, what is less known is the CDC’s attempts to avoid answering many NIEHS and Congress’s complaints.  In a letter to Pediatrics, Dr. Ken Stoller, a UCLA pediatrician and a former fellow of the AAP, noted how then CDC Director Dr. Julie Geberding in the final moments under pressure to give account for the CDC’s wide range of errors in its study stated, “CDC concurs that conducting ecologic analysis using VSD administrative data to address potential associations between thimerosal exposure and the risk of autism spectrum disorder is not useful.”[4]

And here is the rub. Every study the pro-vaccine community quotes to discredit a thimerosal-autism association is either an ecologic study (investigating and comparing statistics between one or more populations) or cohort study (looking at risks or illness in the history of a group or population). Both types of studies are inferior to controlled studies looking at medical conditions in vitro or in vivo. Neither do they follow sound scientific protocol in order to draw definitive conclusions.  Moreover, the most frequent criticism of ecologic and cohort research is the wide scope of deceptive data manipulation such studies lend themselves to in order to arrive at the researcher’s desired result.  For example, in CDC studies, the agency has never compared autism rates in vaccinated children with a population of children who were unvaccinated or had not received mercury laced vaccines.  The lack of such a study should have been a no-brainer for the AAP.

Therefore, if the CDC ecologic study was ruled bogus by its own head of the agency, then why should any credibility be given to other ecologic and cohort studies performed, supported by and/or funded by the CDC.  And it is only such studies that are repeatedly quoted and referred to by thimerosal-autism deniers.

Not a single study in the vaccine industry’s arsenal is biologic. The federal health agencies refuse to conduct convincing biologic studies to bring the thimerosal-autism debate to closure. The reason is simple: there is not an ounce of evidence that such studies would conclude in their favor, otherwise such research would have been performed during this decades long argument.

Nevertheless, independent biologic studies have shown repeatedly that thimerosal is linked to neurological degeneration, including autism, Asperger’s, ADD and ADHD, tics and seizures, etc.  A recent review of all thimerosal research recorded in the National Institutes of Health publication database, PubMed, by the Faculty of Health Sciences at the Universidade de Brasilia in Brazil determined that the biologic data reveals 1) low doses of thimerosal against isolated human and animal brain cells found in all studies characteristic mercury neurotoxicity, 2) there has yet to be studies showing the neurotoxic effects when thimersosal is combined with aluminum, another neurotoxic chemical and common vaccine ingredient, and 3) animal studies show that thimerosal exposure leads to the accumulation of inorganic mercury in the brain.[5]

Dr. Stoller concludes that we now “have a generation of pediatricians, who face perhaps the greatest iatrogenic accident in the history of pediatrics, who actually need to be deprogrammed to understand what the true nature of all neuro-behavioral problems are that they confront without any understanding of etiology or potential interventions.”[6] And the organization mandated to assure America’s pediatricians remain ignorant about the dangers of thimerosal-containing vaccines is the AAP.

A favorite rationale voiced frequently by professional medical associations, such as the AAP and AMA, is since we don’t have conclusive proof to confirm the health risks of a particular vaccine, or chemical found in every day foods and products, or a GM frankenfood, then it is best to side with private industry rather than adopt preventative cautionary measures until such proof is determined.  Common sense unveils this distorted logic, which exonerates the drug, food and chemical industries from having to prove their product is safe before entering the market.

Although AAP has taken positive social stands to improve child welfare, it has failed to protect children from their greatest enemy — the pharmaceutical and chemical industrial complex.  To its credit the Academy has opposed budget reductions affecting the health and welfare of children in poverty; it supports funding that would increase consumption of fruits and vegetables  in school programs, and has supported the removal of school soda vending machines in its fight against obesity. But when addressing the prevention of diseases that directly affect the medical industry, the AAP’s record is dismal.  Among its official recommendations favoring corporate profit rather than promoting pediatric health are the following:

Routine HPV Vaccine.  AAP officially supports the CDC’s recommendation that all males, starting at age 11, be routinely vaccinated with Merck’s quadrivalent human papillomavirus vaccine (Gardasil). Earlier the Academy gave its full approval for routine vaccination of all school aged girls. Since then, Drs. Christopher Shaw and Lucija Tomljenovic at the University of British Columbia have published a peer-review study of their investigation into brain tissues from two New Zealand teenagers who died after Gardasil vaccinations. In both cases, DNA from the vaccine’s HPV virus was found embedded in the girl’s brain cells, which resulted in the likely cause of death. [7]

Psychiatric Drugs for Four-Year Olds.  In 2011, AAP changed their recommendations for prescribing mood-altering psychiatric and psychotropic medications to children.  The Academy reduced the age for diagnosing ADHD to 4 years from its prior threshold of 6 years.  Its recommendations are that behavioral therapy precede administering drugs, in particular Ritalin. Yet this recommendation will unlikely be followed.  Today, less than 20 percent of practicing psychiatrists perform behavioral therapy and prescribing drugs is now the ruling paradigm regardless of age. Ritalin is classified in the same category with cocaine, morphine and opium. Its adverse effects include hallucinations, mania, heart problems and death.  But the AAP seems to be fine with that for pre-schoolers. Then again, the AAP’s chairman for ADHD guidelines, Dr. Mark Wolraich, is a consultant for psychotropic drug companies including Shire Pharmaceutical, Eli Lilly, Shinogi and Next Wave Pharmaceuticals.[8]

Statin Drugs for Children. The Citizens Commission on Human Rights (CCHR) has investigated AAP’s financial ties to the pharmaceutical industry. At the time AAP officially recommended prescribing statin drugs to lower cholesterol for children, it had received over $1.4 million in contributions from major statin makers, including Merck, Abbott and Bristol Myers Squibb.[9]  The Academy also had lowered the minimum age for children to take statins from 10 years to 8 years. Among the statins being prescribed, the FDA expanded warning list of adverse effects to include liver injury, memory loss, increased diabetes risk, and muscle damage.[10]

Genetically Modified Food.  During the autumn 2012 battle in California to mandate labeling of genetically modified foods, AAP fell on the side of Monsanto, DuPont and other agro-chemical corporations. In the Academy’s official report on its position regarding GM produce, it agrees with the seed industry that GM and organic products are nutritionally equivalent.  “Current evidence,’ the report reads, ‘does not support any meaningful nutritional benefits or deficits from eating organic compared to conventionally grown foods, and there are no well-powered human studies that directly demonstrate health benefits or disease protection as a result of consuming an organic diet.”[11]  Neither has the Academy come out publicly to favor the urgent need for safety trials to be conducted on GM foods before entering the food supply.

Milk and Dairy.  In its GMO statement, the AAP claims there are no significant health benefits from organic milk and downplayed the risks posed from growth hormone and estrogen given to dairy cattle. The reports states, “Ingestion of milk from estrogen-treated cows appears to be safe for children.”[12] Apparently the AAP had a moment of unconsciousness during the time studies flooded journals showing that genetically modified bovine growth factor (rBGH) increased IGF-1, which contribute to prostate, breast, colorectum, gastrointestinal and lung cancers.[13]

Pesticides.  The AAP is ambiguous regarding the dangers and health risks of pesticides, although all independent research shows chemical pesticides contribute to serious diseases that are appearing increasing among American children. The Academy’s policy report on GMOs states, “Although chronic pesticide exposure and measurable pesticide metabolites seem undesirable and potentially unhealthy, no studies to date have experimentally examined the causal relationship between exposure to pesticides directly from conventionally grown foods and adverse neurodevelopmental outcomes.”

Water Fluoridation. AAP continues to support the Department of Health and Human Services’ and the Environmental Protection Agency’s commitment to water fluoridation. In 2005, EPA employee unions called for a moratorium on fluoridation programs after a cover-up at Harvard’s School of Dental Medicine leaked and revealed elevated risk of fatal bone cancer in young boys consuming fluoride.  However, the US remains one of the few developed countries that continue the barbaric practice of water fluoridation. Throughout most of Europe, 97% of nation populations drink fluoride-free water. The Swedish government health authorities officially state that there is no credible safety data available to support fluoride; Japan’s official policy is that water fluoridation “may cause health problems.” As early as 1977, Germany’s association of water experts rejected fluoridation” because “the so-called optimal fluoride concentration of 1 mg per liter is close to the dose at which long-term damage to the human body is to be expected.”

* * *

We believe there should be an independent Congressional investigation overseen by experts in immunology and public health science to review all existing studies that have been used as a basis for determining the safety and efficacy of schedules for all vaccines. We propose a long-term human study comparing one group of vaccinated people following existing protocols and another group given no vaccines, followed on a three month basis for five years, to determine which group is provided with a statistically significant benefit. However, no one affiliated with the study should have any direct or indirect financial ties to any vaccine industry or pharmaceutical interest nor should anyone be selected who has shown previous bias on the topic.

Richard Gale is the Executive Producer of the Progressive Radio Network and a former Senior Research Analyst in the genomic industry. Dr. Gary Null is the host of the nation’s longest running public radio program on nutrition and natural health and a multi-award-winning director of progressive documentary films, including Vaccine Nation and Autism: Made in the USA.

Notes

[1]  Levin, Myron “Battle Lines Drawn Over Mercury in Shots” Los Angeles Times, April 10, 2006)

[2]  Tavernise, S  “Vaccine Rule is Said to Hurt Health Efforts”  New York Times, December 17, 2012

[3]  Stoller, K  http://adventuresinautism.blogspot.com/2008/06/ken-stollers-letter-to-pediatrics-on.html

[4]  Ibid.

[5]  Dorea JG. “Integrating Experimental (In Vitro and In Vivo) Neurotoxicity Studies of Low-dose Thimerosal Relevant to Vaccines” Neurochem Res. 2011 Feb 25.

[6] Stoller, K  op cit.

[7]  Tomljenovic L, Shaw C. “Death after Quadrivalent Human Papillomavirus (HPV) Vaccination: Causal or Coincidental?” Pharmaceutical Regulatory  Affairs, doi.org/10.4172/2167-7689.S12-001

[8]  Citizens Commission on Human Rights “American Academy of Pediatrics Promotes Big Pharma Agenda Drugging 4-year-olds” October 17, 2011  http://www.cchrint.org

[9]  Ibid

[10]  “FDA Expands Advice on Statin Risks”  http://www.fda.gov/ForConsumers/ConsumerUpdates/ucm293330.htm

[11]  Forman J, Silverstein J, “Organic Foods: Health and Environmental Advantages and Disadvantages” http://pediatrics.aappublications.org/content/early/2012/10/15/peds.2012-2579

[12]  Petersen A, “Report Supports Organic Produce but Not Milk” Wall Street Journal, October 22, 2012

[13]  Food and Water Watch, “rBGH: What the Research Shows” http://www.foodandwaterwatch.org/factsheet/what-research-shows/

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December 22, 2012 Posted by | Deception, Science and Pseudo-Science, Timeless or most popular | , , , , , , | Leave a comment

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