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Internal CDC Documents Reveal They Manipulated Data To Conceal A Link Between Autism & Vaccines

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A Foolish Faith In Authority Is The Worst Enemy Of The Truth”– Albert Einstein

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By Vera Sharav

Note from the World Mercury Project Team:  Following is Part Six in Vera Sharav’s seven-part exposé of the complex and widespread corruption that exists in the vaccination program, the deceptive practices by officials of “authoritative” international public health institutions and further evidence of the callous disregard for the plight of thousands of children and young adults who suffer irreversible harm. Sharav’s research is a must-read by those in our community.

You can read the previous parts here

This recourse to authority is an attitude reminiscent of the American eugenics movement, when public health officials and academics at elite universities, embraced the pseudo-scientific tenets of eugenics, which were the basis for abhorrent discriminatory policies, including forced sterilization policies that were launched in the USA.[60]

The internal CDC documents reveal that in addition to major methodological flaws and inconsistencies, CDC scientists and Danish scientists collaborated in outright fraud. Thorsen and his co-authors manipulated the results by excluding the largest outpatient clinic in Copenhagen – comprising 20% of autism cases in Denmark – from the pre-1992 cohort – thereby artificially inflating the autism incidence in Denmark after 1992 when thimerosal had been eliminated from children’s vaccines.

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Furthermore, the authors of the Pediatrics (2003) article falsified their findings by omitting the 2001 data from their published report. The published report claims an astoundingly high (implausible) increase in the autism prevalence rate in Denmark after the phase-out and removal of thimerosal between 1990 and 1999.

This case reveals much about the corrupted vaccine literature. Indeed, the research community has not only failed to examine Thorsen / CDC research fraud, journal editors are knowingly facilitating fraudulent research articles to influence vaccination policies that put thousands of children at risk, depriving them of living normal lives.

The publicly accessible, internal CDC correspondence[1] allows anyone to trace the underhanded route that led to the publication of the Madsen/Thorsen/ et al report in the journal Pediatrics – after it was rejected by the Lancet and by JAMA. A written communication between Dr. Thorsen and high ranking CDC official, Coleen Boyle (2003) reveals that when the paper was first submitted to Pediatrics with the 2001 data included; it was criticized by one peer-reviewer:

“The drop of incidence shown for the most recent years is perhaps the most dramatic feature of the figure, and is seen in the oldest age group as well as the youngest.” The reviewer questions the authors’ failure to discuss “the possibility that this decrease might have come about through elimination of [T]himerosal.”

The internal CDC documents further show that CDC brought pressure to bear on journal editors to publish the Danish studies. Dr. Cordero, Assistant Surgeon General, National Center on Birth Defects & Developmental Disabilities used his influence to persuade Dr. Lucey to publish the Madsen / Thorsen study, “Thimerosal and the Occurrence of Autism”

“I am writing in support of an expedited review and consideration of the enclosed manuscript… Specific aspects of vaccinations have been subject to inquiry includ[ing] the MMR vaccine and thimerosal…For thimerosal there are limited data…The Danish study is a powerful epidemiologic study …a key strength of the study is the ability to examine rates of autism prior to and after the discontinuation of vaccines containing thimerosal in Denmark in 1992. Contrary to what would be expected if thimerosal was linked to autism, the authors did not observe a decline in the rate of autism with the removal of thimerosal…

Its findings provide one strong piece of evidence that thimerosal is not causally linked to autism.” [Exhibit V: Cordero letter to Lucey]

How is it that even as thousands of journal papers are retracted from the scientific record – Retraction Watch counted more than 14,000 retractions– some are retracted for spurious reasons, others provide no  explanation – yet, deliberately manipulated, fraudulent reports that were crafted to conceal vaccine safety hazards, have never been removed from the scientific literature. In fact, they continue to influence public health policy inasmuch as they were published in “authoritative”  “high impact” journals.

  • In the case of Pediatrics, a fraudulent study was published despite the fact that its editors knew that the 2001 data was omitted from the final version.
  •  US public health officials not only failed to disavow the fugitive’s research, federal officials have continued to collaborate and to co-author papers with him.
  • Dr. Thorsen continues to collaborate with the Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Research Network.
  • Federal dollars continued to flow to studies in which he was or is involved.
  • Thorsen is the named author of at least 19 reports following his fugitive status – “after his “disappearance”. The journals include: Pediatric Neurology (2016), PLoS One (2015), Pediatric Research (2014), Journal of Autism Development (2013), PLoS One (2013) (NCBI search)
  • Both the HHS and DOJ continue to use his research as grounds to reject vaccine injury claims in the National Vaccine Injury Compensation.
  • No retraction of the articles he was associated with during and subsequent to his 2004 to 2010 alleged criminal activities has occurred.
  • The entire US public health machine acts as if the indictment never occurred.

Public health officials and the news media are using fear and exaggeration about the risks of infectious disease in the U.S., as well as the risks posed by un-vaccinated children, which is pitting neighbor against neighbor and parent against parent. They use the classic divide and conquer strategy.

Dr. Paul Offit, director of the Vaccine Education Center at Children’s Hospital of Philadelphia (CHOP), responded to Thorsen’s indictment stating:

“even if the allegation against Thorsen is true, it does not mean his science is bad… Let’s assume it is true that he embezzled money, the notion that it casts the science into question is false.For these big epidemiological studies, it is hard to believe that one person could effectively change the data.” (Philadelphia Inquirer, March 2010)

Dr. Offit is considered to be a leading authority, an ardent and outspoken vaccine defender/ promoter. This statement encapsulates the low regard that vaccinologists have for the integrity of vaccine science. Of course, like most vaccine promoters, Dr. Offit’s blatant conflicts of interest have enabled him to “vote himself rich”. [61]He is quoted in Newsweek (2008) stating that the millions he made from the rotavirus vaccine patent: “was like winning the lottery.

I believe that even if the allegations of embezzlement are not true, the evidence is indisputable that the studies produced by Poul Thorsen, and published in premier medical journals, are fatally flawed. By altering the inclusion criteria, excluding data that contradicted the authors’ claimed conclusion relegated the study to the ash heap of fraudulent junk science.

Furthermore, the following two studies “were conducted and results published without legally–required ethics clearances.”

CDC officials knew that the psychiatric registry records were reviewed without required permissions and they covered it up. In what are completely unethical acts by all involved, the team members went into damage control mode and decided that they likely could obtain permission for ongoing and future studies.

They concluded that it would probably be impossible to get permission for research that was already finalized (and published). It is absurd that experienced federal grants management officials even discussed the idea of seeking a human subject safety review retroactively. These are serious ethical violations. [sic] they shed light on the pervasive culture of corruption at the CDC.[62]

In January 2013, a Congressional hearing on autism[63] convened by the Government Oversight Committee.

Dr. Coleen Boyle (had by then been promoted to) Director of the National Center on Birth Defects and Developmental Disabilities, and Dr. Alan Guttmacher, Director of the Eunice Kennedy Shriver Institute of the National Institute of Child Health & Human Development (NICHD) defended their agencies but provided no substantive information.

Boyle and Guttmacher evaded pertinent questions. When asked about why the number of children with autism has surged, they testified that autism has no known cause or cure; their focus was statistical tracking and detection tools.

  • When asked if CDC had sought constituent input?
  • Are there studies looking at the very aggressive way that we’re over-vaccinating our children”?
  • Are you looking at the impacts of combinations of vaccines”?
  • Boyle responded, “We know that vaccines save lives.”
  • No response was given to the following questions:
  • What steps were taken to ensure the integrity of the studies in which Thorsen was involved?
  • Why did the FDA and HHS take thimerosal out of all children’s vaccines except just the one or two or three, if there was no problem?
    Both Republicans and Democrats were exasperated by the evasive responses.
  • Dr. Boyle finally acknowledged: “We have not studied vaccinated versus unvaccinated [children]”.

Dr. Guttmacher tried to impress the committee with non-specific claims of accomplishments: the NIH $169 million budget allocation for autism in 2011; he claimed “effective interventions…recent advances in networks” but could not give an example of an effective autism treatment resulting from the last 10 yrs in which the NIH had spent $500 million dollars on autism research, Dr. Guttmacher responded that progress had been “elusive” due to lack of funding. He did not wish to respond to the question, why thimerosal was still used in multi-vial vaccinations?

“I’m just sitting here, and I’m listening to all this. There’s something wrong with this picture. There’s something wrong… When you’ve got this combination of shots, and you go from 1 in 10,000 to 1 in 88, it seems to me somebody would say, wait a minute, let’s put the brakes on this, and at least let’s try to figure out whether the multiple-shot situation is causing this —

If I’m giving a baby nine shots in a day whether that—I mean, how much impact that’s having… you said there’s a body of evidence with regard to vaccines…

Mr. Chairman, I don’t know where we go from here… if we’re going to err, let’s err on the side of keeping children safe even if we have to [sic] do a pause and give one shot a day.”

Mark Blaxill, the author of The Age of Autism (2010), which documents that autism did not exist before the introduction of vaccines in the 1930s. Blaxill presented testimony on behalf of Safe Minds:

Autism is a public health crisis of historic proportions. Autism is a public health crisis of historic proportions. Worse than poliomyelitis. It’s devastating a generation of children and their families. We need to face up to the reality Autism is a national emergency. Autism rates didn’t just rise, they multiplied.The old surveys didn’t just miss 99% of children with autism.

It’s horrible but true; reported rates of autism have risen simply because there are more cases of autism. In the midst of this crisis, the federal agencies responsible for the health of our nation’s children have failed in their duty. CDC’s negligence has led the way. Many believe CDC has actively covered up the evidence surrounding autism’s environmental causes.

 NIH has received the lion’s share of Congressional funding, money they have wasted on status quo research and gene studies. It’s absurd to focus on genetic research in this crisis, there’s no such thing as a genetic epidemic. In the financial world, the result of the pressure to manipulate numbers to provide the answers bosses want has a name – securities fraud…what CDC has given us is the medical equivalent of securities fraud. All to avoid the inconvenient reality of the autism epidemic.

In 2006, Congress gave the NIH a mission to “combat autism.” You authorized $850 million for that mission… NIH spent most of that money on the great autism gene hunt while blackballing environmental researchers and defying parent concerns. It’s been a colossal waste of money and time. Not a single case of autism has been prevented. Not a single child received improved treatments. We need to conduct independent research into the great unmentionables, mercury, and vaccines, connections that we’ve documented in the earliest cases.

 We need accountable new leadership. Please root out the failures, the waste, the fraud, the negligence and the abuse of these agencies that aren’t doing their jobs.”  Blaxill’s latest book, co-authored by Dan Olmsted is DENIAL: How Refusing to Face the Facts about Our Autism Epidemic Hurts Children, Families, and Our Future (2017)  

Cong. Bill Posey made an announcement, and submitted new information for the Congressional Record: “I have information that the fugitive doctor had been involved in [sic] 21 of the 24 studies with CDC”.

Another Major Episode of CDC Fraud & Scientific Malfeasance Came to Light

In 2014, Dr. William Thompson, the senior CDC epidemiologist who co-authored the 2004 study published in Pediatrics blew the whistle and revealed that fraud had been committed by CDC authors (himself included) to conceal the higher risk of autism for African American baby boys who were vaccinated prior to 36 months and prior to 24 months of age. Beginning in 2013, in taped conversations with Dr. Brian Hooker, Dr. Thompson revealed how CDC destroyed evidence of the risk for autism. He provided primary documented evidence – a copy of data that had been deleted from the published article in Pediatrics (2004) the journal of the American Academy of Pediatrics.[64]

“We hypothesized that if we found statistically significant effects at either the 18-month or 36-month threshold, we would conclude that vaccinating children early with the MMR vaccine could lead to autism-like characteristics or features.”

When CDC scientists did find a statistically significant causal relationship between MMR and autism in African American boys, according to Dr. Thompson’s eyewitness account, CDC removed 260 black baby boys from the dataset and destroyed the data. The analysis in the published report in Pediatrics misrepresents the risk of having eliminated data from the dataset. That constitutes fraud.

Dr. Thompson stated that he wrote a letter alerting Dr. Julie Gerberding to the findings and suggested that the Institute of Medicine safety review committee should be informed of the risk, prior to its consequential February 2004 meeting. Dr. Thompson was reprimanded for contacting Dr. Gerberding and was put on administrative leave. He was threatened with being fired.  In his taped conversation with Dr. Hooker – which was central in the film Vaxxed – he expressed shock by his own action:[65]

“Oh my God. I cannot believe we did what we did. But we did.” “It’s the lowest point of my career, when I went along with that paper. I went along with this, and we didn’t report significant findings.”

“I am completely ashamed of what I did. I have great shame now. I was complicit, and I went along with that paper. I have great shame now, when I meet families with kids with autism, because I have been part of the problem.”

Dr. Hooker re-analyzed the complete CDC dataset in 2014, including the data that had been omitted from the published study in Pediatrics (2004). It showed statistically significant adverse effects at both 24 months and 36 months (RR 3.36, 95% CI 1.50-7.51, p = 0.0019).  The higher relative risk of autism for African American infant boys, vaccinated with MMR prior to 36 months, was (330%) compared to other babies. His re-analysis was published online by Translational Neurodegeneration on August 8, 2014:[65]

“The present study provides new epidemiologic evidence showing that African American males receiving the MMR vaccine prior to 24 months of age or 36 months of age are more likely to receive an autism diagnosis.

The results show a strong relationship between child age at the administration of the first MMR and autism incidence exclusively for African American boys which could indicate a role of the vaccine in the etiology of autism within this population group. The particular analysis was not completed in the original Destefano et al (CDC) study… the CDC study limited the total African American cohort to include only those individuals who possessed a valid State of Georgia birth certificate which decreased the statistical power of their analysis.”

However, Dr. Hooker’s article came under attack; pressure from the shadowy cyber enforcement squads,[66] that act as a police force to suppress every independent vaccine study that challenges the mantra: “there is no link to autism… vaccines are safe and effective”.

On August 27, the journal removed Hooker’s article with the statement: “This article has been removed from the public domain because of serious concerns about the validity of its conclusions. The journal and publisher believe that its continued availability may not be in the public interest”. There was no specific fault or mistake cited.[68]

On the same day that Dr. Hooker’s article was removed from the journal’s website, Dr. Thompson acknowledged the following in a statement issued by his lawyer (August 27, 2014):

“I regret that my co-authors and I omitted statistically significant information in our 2004 article published in the journal Pediatrics. The omitted data suggested that African American males who received the MMR vaccine before age 36 months were at increased risk for autism. Decisions were made regarding which findings to report after the data were collected, and I believe that the final study protocol was not followed.”

“My concern has been the decision to omit relevant findings in a particular study for a particular subgroup for a particular vaccine. There have always been recognized risks for vaccination and I believe itis the responsibility of the CDC to properly convey the risks associated with receipt of those vaccines.

I have had many discussions with Dr. Brian Hooker over the last 10 months regarding studies the CDC has carried out regarding vaccines and neurodevelopmental outcomes, including autism spectrum disorders. I share his belief that CDC decision-making and analyses should be transparent.”

Dr. Thompson then forwarded the documents to a U.S. Congressman William Posey who has repeatedly requested a congressional investigation.[69]

“Mr. Speaker, I believe it is our duty to insure that the documents that Dr. Thompson are not ignored. Therefore I will provide them to members of Congress and the House Committees upon request. Considering the nature of the whistleblower’s documents as well as the involvement of the CDC, a hearing and a thorough investigation is warranted.“So I ask, Mr. Speaker, I beg, I implore my colleagues on the appropriations committees to please, please take such action.”

On August 26, 2014, Sharyl Attkisson, an investigative journalist who earned numerous awards as CBS science correspondent (1993-2014), conducted taped telephone interviews with Dr. Frank DeStefano,[70] Director of CDC Immunization Safety, who co-authored the Pediatrics (2004) study.

He confirmed the verity of the confessions of CDC whistleblower, Dr. William Thompson about the omission from the published Pediatrics report, of children in the dataset, for whom there were no birth certificates here.

In a telephone interview, DeStefano defended the study and reiterated the commonly accepted position that there’s no “causal” link between vaccines and autism. But he acknowledged the prospect that vaccines might rarely trigger autism.

“Wouldn’t say it’s a myth, I’d say[sic] all the evidence, thus far, points to that there’s not a causal association between vaccines and autism…It’s a theoretical possibility…It’s hard to predict who those children might be, but certainly, individual cases can be studied to look at those possibilities.”

Attkisson writes, “They’re not even trying. A CDC spokesman told me that:

“the agency is not currently investigating the relation between vaccines and autism spectrum disorders (ASD). Further, CDC does not have any planned research addressing vaccines and autism. CDC believes that this topic has been thoroughly studied and no causal links have been found. Current CDC ASD related research focuses on determining how many people have ASD and understanding [other, not vaccine-related] risk factors and causes for ASD”.[71]

When Dr. Thompson attempted to leave, CDC gave him a $24,000 bonus – a retention fee. Apparently, CDC continues to employ Dr. Thompson, because they feel more secure with him as an agency employee, enabling them to scrutinize his activities.  Clearly, they feared his being outside the agency, which would risk that he might disclose additional CDC secrets.

CDC Continues to Conceal the Authentic 1999 Verstraeten VSD Study Findings.

When a request was filed with CDC to provide Dr. Verstraeten’s original dataset for independent analysis, CDC officials claimed the data were “lost.”  Even after approval was granted, Dr. Mark Geier was blocked from gaining access to CDC’s Vaccine Safety Dataset which is the data CDC relied upon its study published Pediatrics.  CDC continues to disseminate false reassurances in its “Science Summary Fact Sheet” claiming: “The evidence is clear: thimerosal is not a toxin in vaccines… there is no relationship between thimerosal-containing vaccines and autism in children.” As its “evidence,” CDC cites the Danish studies.

In January 2017, the President and Executive Vice President of the American Academy of Pediatrics issued a press release in opposition to a federal vaccine commission on immunizations.

Fernando Stein, MD, FAAP and Karen Remkey, MD, MBA, MPH, FAAP stated: since we already know that: “vaccines are safe. Vaccines are effective. Vaccines save lives.” AAP declared that there is no need for further examination pf vaccine safety:

  • Vaccines prevent forms of cancer.
  • Claims that vaccines are linked to autism have been disproven by a robust body of medical literature.
  • Claims that vaccines are unsafe when administered according to the [CDC’s] recommended schedule have likewise been disproven by a robust body of medical literature”.

However, when asked to provide citations to any peer-reviewed study that supports AAP’s claim that “vaccines prevent forms of cancer” or to cite the “robust body of medical literature” that supports its claims, the AAP declined, with a “no comment” response. (Immunization News, 2017)

WMP NOTE:  This concludes Part Six. The final segment of this series will be entitled:  Multiple Industry-Saturated Collaborating Partners Set the Agenda for Vaccination Policies.

Previously published articles: Sharav’s Introduction to the full article,  L’affaire Wakefield: Shades of Dreyfus & BMJ’s Descent into Tabloid Science, outlines her well-researched and documented belief that, “Public health officials and the medical profession have abrogated their professional, public, and human responsibility, by failing to honestly examine the iatrogenic harm caused by expansive, indiscriminate, and increasingly aggressive vaccination policies.” Part One focuses on how the Centers for Disease Control and Prevention (CDC) and the vaccine industry control vaccine safety assessments, control the science of vaccines and control the scientific and mass channels of information about vaccines. In Part Two Ms. Sharav interprets the complex web of internal CDC documents, revealing how key CDC studies and CDC-commissioned studies were shaped by use of illegitimate methods. Part Three takes a closer look at the Brighton Collaboration and the extraordinary influence these stakeholders have in the business of vaccines and their power to control the science and research and manipulate reports to further their own interests. Focusing on the HPV vaccine, in Part FourMs. Sharav explores how a global network of government/academic and industry stakeholders can suppress information about genuine scientific findings and, when needed, engage in corrupt practices to thwart the airing of information about vaccine safety issues. CDC’s childhood vaccination policy rests on the denial of safety hazards posed by vaccines and CDC officials are intent on shielding the policy and vaccination schedule at any cost. Part Fiveexamines documentation and internal correspondence that reveals how CDC used its influence and subsequently rejected scientific studies that contradicted the sacrosanct vaccine safety mantra.

More about the author: Vera Sharav is a Holocaust survivor and a fierce critic of the medical establishment. This article was originally published at www.ahrp.org. Stat news recently published an article about her and her work. 

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Awareness

Studies Show We Can Heal With Sound, Frequency & Vibration

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In Brief

  • The Facts:

    Multiple studies and examples have shown how sound, frequency and vibration can literally alter physical material matter. Research has also shown that sound, frequencies and vibration can be used as a significant healing method for various ailments.

  • Reflect On:

    How plausible would it be for these interventions to become a regular part of therapy, just as much as pharmaceutical drugs are now?

Cymatics is a very interesting topic. It illustrates how sound frequencies move through a particular medium such as water, air, or sand and as a result directly alter physical matter. There are a number of pictures all over the internet as well as youtube videos that demonstrate how matter (particles) adjust to different sounds and different frequencies of sound.

When it comes to ancient knowledge, sound, frequency and vibration have always been perceived as powerful forces that can influence and alter life all the way down to the cellular level. Sound healing methods are often used by Shamans, who employ drums and singing to access trance states. Research has even demonstrated that drumming and singing can can be used to slow fatal brain disease, and it can generate a sense of oneness with the universe . Sound therapy is getting more popular, and it can have many medical applications, especially within the psychological and mental health realms.

Sound, frequency and vibration are used all throughout the animal kingdom, and there are many examples. If we look at the wasp, they use antennal drumming to alter the caste development or phenotype of their larvae. Conventional thinking has held for quite some time that differential nutrition alone can explain why one larvae develops into a non-reproductive worker and one into a reproductive female (gyne).  However, this is not the case, according to a 2011 study:

“But nutrition level alone cannot explain how the first few females to be produced in a colony develop rapidly yet have small body sizes and worker phenotypes. Here, we provide evidence that a mechanical signal biases caste toward a worker phenotype. In Polistes fuscatus, the signal takes the form of antennal drumming (AD), wherein a female trills her antennae synchronously on the rims of nest cells while feeding prey-liquid to larvae. The frequency of AD occurrence is high early in the colony cycle, when larvae destined to become workers are being reared, and low late in the cycle, when gynes are being reared. Subjecting gyne-destined brood to simulated AD-frequency vibrations caused them to emerge as adults with reduced fat stores, a worker trait. This suggests that AD influences the larval developmental trajectory by inhibiting a physiological element that is necessary to trigger diapause, a gyne trait.”

This finding indicates that the acoustic signals produced through drumming within certain species carry biologically meaningful information (literally: ‘to put form into’) that operate epigenetically (i.e. working outside or above the genome to affect gene expression).

Pretty fascinating, isn’t it? Like many other ancient lines of thought, this has been backed by modern day scientific research.

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Cancer 

Another example comes from cancer research. In his Tedx talk, “Shattering Cancer with Resonant Frequencies,” Associate Professor and Director of Music at Skidmore College, Anthony Holland, tells the audience that he has a dream. That dream is to see a future where children no longer have to suffer from the effects of toxic cancer drugs or radiation treatment, and today he and his team believe they have found the answer, and that answer is sound. Holland and his team wondered if they could affect a cell by sending a specific electric signal, much like we do with LCD technology. After searching the patent database for a device that could accomplish this, they came across a therapeutic device invented by New Mexico physician Dr. James Bare. The device uses a plasma antenna that pulses on and off, which, as Holland explains, is important because a constant pulse of electricity would produce too much heat and therefore destroy the cell. For the next 15 months, Holland and his team searched for the exact frequency that would directly shatter a living microorganism. The magic number finally came in the form of two inputs, one high frequency and one low. The high frequency had to be exactly eleven times higher than the low, which in music is known as the 11th harmonic. At the 11th harmonic, micro organisms begin to shatter like crystal glass.

After consistently practicing until they became efficient at the procedure, Holland began working with a team of cancer researchers in an attempt to destroy targeted cancer cells. First they looked at pancreatic cancer cells, eventually discovering these cells were specifically vulnerable between 100,000 – 300,000 Hz.

Next they moved onto leukemia cells, and they were able to shatter the leukemia cells before they could divide. But, as Holland explains in his talk, he needed bigger stats in order to make the treatment a viable option for cancer patients.

In repeated and controlled experiments, the frequencies, known as oscillating pulsed electric field (OPEF) technology, killed an average of 25% to 40% of leukemia cells, going as high as 60% in some cases. Furthermore, the intervention even slowed cancer cell growth rates up to 65%.

You can read more about the story, find sources, and watch that TEDx talk here.

Another example occurred in  1981, when biologist Helene Grimal partnered with composer Fabien Maman to study the relationship of sound waves to living cells. For 18 months, the pair worked with the effects of 30-40 decibel sounds on human cells. With a camera mounted on a microscope, the researchers observed uterine cancer cells exposed to different acoustic instruments (guitar, gong, xylophone) as well as the human voice for 20-minute sessions.

They discovered that, when exposed to sound, cancer cells lost structural integrity until they exploded at the 14-minute mark. Far more dramatic was the sound of a human voice — the cells were destroyed at the nine-minute mark.

After this, they decided to work with two women with breast cancer. For one month, both of the women gave three-and-a-half-hours a day to “toning” or singing the scale. Apparently, the woman’s tumor became undetectable, and the other woman underwent surgery. Her surgeon reported that her tumor had shrunk dramatically and “dried up.” It was removed and the woman had a complete recovery and remission.

These are only a few out of multiple examples that are floating around out there.

Let’s not forget about when Royal Rife first identified the human cancer virus using the world’s most powerful microscope. After identifying and isolating the virus, he decided to culture it on salted pork. At the time this was a very good method for culturing a virus. He then took the culture and injected it into 400 rats, which, as you might expect, created cancer in all 400 rats very quickly. The next step for Rife was where things took an interesting turn. He later found a frequency of electromagnetic energy that would cause the cancer virus to diminish completely when entered into the energy field.  You can read more about that story here.

More Research

A 2014 study published in the Journal of Huntington’s Disease found that two months of drumming intervention in Huntington’s patients (considered an irreversible, lethal neurodegenerative disease) resulted in “improvements in executive function and changes in white matter microstructure, notably in the genu of the corpus callosum that connects prefrontal cortices of both hemispheres.” The study authors concluded that the pilot study provided novel preliminary evidence that drumming (or related targeted behavioral stimulation) may result in “cognitive enhancement and improvements in callosal white matter microstructure.”

A 2011 Finnish study observed that stroke patients who were given access to music as cognitive therapy had improved recovery. Other research has shown that patients suffering from loss of speech due to brain injury or stroke regain it more quickly by learning to sing before trying to speak. The phenomenon of music facilitating healing in the brain after a stroke is called the “Kenny Rogers Effect.”

A 2012 study published in Evolutionary Psychology found that active performance of music (singing, dancing and drumming) triggered endorphin release (measured by post-activity increases in pain tolerance), whereas merely listening to music did not. The researchers hypothesized that this may contribute to community bonding in activities involving dance and music-making.

According to a study published by the National Institute of Health, “Music effectively reduces anxiety for medical and surgical patients and often reduces surgical and chronic pain. [Also,] Providing music to caregivers may be a strategy to improve empathy, compassion, and care.” In other words, music is not only good for patients, it’s good for those who care for them as well.

Below is an interesting interview with Dr. Bruce Lipton. You can view his curriculum vitae here.

The Takeaway

The information presented in this article isn’t even the tip of the iceberg when it comes the the medical applications of sound, frequency and vibration, which are all obviously correlated. One thing is clear, however, which is that there are many more methods out there, like the ones discussed in this article, that should be taken more seriously and given more attention from the medical establishment. It seems all mainstream medicine is concerned about is making money and developing medications that don’t seem to be representative of our fullest potential to heal. “Alternative” therapies shouldn’t be labelled as alternative, they should be incorporated into the norm.

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Awareness

Mental Health Problems—The Sad “New Normal” on College Campuses

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College campuses are witnessing record levels of student mental health problems, ranging from depression and anxiety disorders to self-injurious behaviors and worse. A clinician writing a few years ago in Psychology Today proclaimed it neither “exaggeration” nor “alarmist” to acknowledge that young Americans are experiencing “greater levels of stress and psychopathology than any time in the nation’s history”—with ramifications that are “difficult to overstate.”

The problems on college campuses are manifestations of challenges that begin sapping American children’s health at younger ages. For example, many students enter college with a crushing burden of chronic illness or a teen-onset mental health diagnosis that has made them dependent on psychotropic or other medications. The childhood prevalence of different forms of cognitive impairment has also increased and is associated with subsequent mental health difficulties. In addition, a majority of American students are now unprepared academically for their college careers, as evidenced by historically low levels of achievement on standardized tests. Once in college, large proportions of students—increasingly characterized as emotionally fragile—blame mental health challenges for significantly interfering with their ability to perform. The outcomes of these trends—including rising suicide rates among students and declining college completion rates—bode poorly for young people’s and our nation’s future.

… more than three in five (63%) respondents reported experiencing overwhelming anxiety in the past year, while two in five (42%) reported feeling so depressed that it was difficult to function.

Crippling anxiety and depression

A 2018 survey at 140 educational institutions asked almost 90,000 college students about their health over the past 12 months. The survey found that more than three in five (63%) respondents reported experiencing “overwhelming anxiety” in the past year, while two in five (42%) reported feeling “so depressed that it was difficult to function.” Students also reported that anxiety (27%), sleep difficulties (22%) and depression (19%) had adversely affected their academic performance.

In the same survey, 12% of college students reported having “seriously considered suicide.” Another study, which looked at college students with depression, anxiety and attention-deficit/hyperactivity disorder (ADHD) who had been referred by college counseling centers for psychopharmacological evaluation, found that the same proportion—12%—had actually made at least one suicide attempt. Half of the students in the latter study had previously received a prescription for medication, most often antidepressants.

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Colleges are feeling the squeeze, with demand growing nationally for campus mental health services. A study by Penn State’s Center for Collegiate Mental Health reported an average 30% to 40% increase in students’ use of counseling centers between 2009 and 2015 at a time when enrollment grew by just 5%. According to Penn State’s report, the “increase in demand is primarily characterized by a growing frequency of students with a lifetime prevalence of threat-to-self indicators.”

College vaccines

Most colleges expect new students to have had the full complement of CDC-recommended childhood vaccines and to top up before college matriculation with any vaccines or doses that they may have previously missed. In particular, universities are likely to emphasize tetanus-diphtheria-pertussis (Tdap) and measles-mumps-rubella (MMR) boosters; the human papillomavirus (HPV) vaccine; meningococcal vaccination; and annual flu shots.

… found particularly strong associations for three disorders common on college campuses—anorexia nervosa, obsessive-compulsive disorder and anxiety disorders—and observed a surge in diagnosed disorders after influenza vaccination (one of the vaccines that college students are most likely to get).

It is unlikely that clinics are issuing warnings to freshly vaccinated college students about potential adverse consequences to watch out for, yet two universities (Penn State and Yale) made news in 2017 when their researchers published a study showing a temporal relationship between newly diagnosed neuropsychiatric disorders and vaccines received in the previous three to twelve months. Although the researchers analyzed health records for 6- to 15-year-old children, not college students, they found particularly strong associations for three disorders common on college campuses—anorexia nervosa, obsessive-compulsive disorder and anxiety disorders—and observed a surge in diagnosed disorders after influenza vaccination (one of the vaccines that college students are most likely to get). They also detected significant temporal associations linking meningitis vaccination to both anorexia and chronic tic disorders.

To distance themselves from too strongly implicating vaccines, these researchers later proposed several less controversial mechanisms to explain their findings, including the presence of predisposing inflammatory or genetic factors. One of the researchers even suggested that the “trauma” of getting “stuck with needles” might be triggering the adverse neuropsychiatric outcomes.

This absurd sidestepping ignores considerable experimental evidence from both animals and humans linking the immune responses produced by vaccines (and vaccine adjuvants) to adverse mental health symptoms. In fact, some researchers vaccinate healthy animals or people on purpose just to study this phenomenon. For example:

  • A study intentionally injected mice with the vaccine used against tuberculosis (BCG vaccine) to induce “depression-like behavior,” finding that the vaccine-induced depression was resistant to treatment with standard antidepressants.
  • Another study in mice found that both the antigens and the aluminum adjuvant in the Gardasil HPV vaccine produced significantly more behavioral abnormalities, including depression, in the exposed mice compared to unexposed mice.
  • University of California researchers followed healthy undergraduates for one week before and one week after influenza vaccination; in the absence of any physical symptoms, they detected increased post-vaccination inflammation that was associated with more mood disturbances—especially “depressed mood and cognitive symptoms.”
  • Another study of influenza vaccination compared vaccine recipients who had preexisting depression and anxiety to “mentally healthy” recipients, finding that both groups had “decreased positive affect” following vaccination; however, the vaccine’s impact on mood was “more pronounced for those with anxiety or depression.”
  • Neuroscientists at Oxford injected healthy young adults with typhoid vaccine to explore “the link between inflammation, sleep and depression,” finding that the vaccine “produced significant impairment in several measures of sleep continuity” in the vaccine group compared to placebo; the researchers noted in their conclusions that impaired sleep is both a “hallmark” and “predictor” of major depression.
  • Another group of UK researchers who likewise injected healthy young adult males with the typhoid vaccine found that, within hours, the vaccine had produced measurable social-cognitive deficits.

Interestingly, a study conducted in 2014 found that vaccine-mental health effects may cut both ways. Researchers who assessed self-reported depression and anxiety (and other measures) in 11-year-olds before and up to six months after routine vaccination found that children who reported more initial depressive and anxious symptoms had a stronger vaccine response(defined by “elevated and persistently higher antibody responses”) and that this association remained even after controlling for confounders. Given that this type of overactive vaccine response can be a harbinger of autoimmunity, some researchers have urged more attention to these “bidirectional” effects.

… we are kidding ourselves if we ignore the possible contribution of a cumulative vaccine load that has children receiving dozens of doses by age 18 …

afe spaces or safe vaccines?

As “safe spaces” multiply on college campuses, and elite private institutions offer dumbed-down for-credit courses like “The Sociology of Miley Cyrus” or “Beginning Dungeons and Dragons,” it is time to take stock of the health challenges—both mental and physical—that are sabotaging college students’ chances of success. Researchers already have noted a disturbing mismatchbetween available cognitive abilities and the types of “non-routine analytical-cognitive” skills that our nation will increasingly need in the future. While variables such as student debt certainly factor into college students’ stress equation, we are kidding ourselves if we ignore the possible contribution of a cumulative vaccine load that has children receiving dozens of doses by age 18—and piles on even more when kids go off to college.


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Awareness

Vaccine Rhetoric vs. Reality—Keeping Vaccination’s Unflattering Track Record Secret

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Note: This is Part VI in a series of articles adapted from the second Children’s Health Defense eBook: Conflicts of Interest Undermine Children’s Health. The first eBook, The Sickest Generation: The Facts Behind the Children’s Health Crisis and Why It Needs to End, described how children’s health began to worsen dramatically in the late 1980s following fateful changes in the childhood vaccine schedule.]

A concerted and “heavy-handed” effort is under way to censor information that contradicts the oversimplified sound bites put forth by public health agencies and the media about vaccines. However, while brazen, in-your-face censorship—and attacks on health freedom—have ratcheted up to an unprecedented degree,  officialdom’s wish to keep vaccination’s unflattering track record out of the public eye is nothing new.

There is a chasm between vaccine rhetoric and reality for most if not all vaccines, but four vaccines—varicella (chickenpox), rotavirus, human papillomavirus (HPV) and pertussis-containing vaccines—offer especially instructive before-and-after case studies. Analysis of the U.S. experience with these vaccines raises important questions. First, why did the Food and Drug Administration (FDA) race to approve—and why does the Centers for Disease Control and Prevention (CDC) heavily promote—vaccines such as varicella and rotavirus when there is little public health justification for them? Second, why are federal agencies ignoring the many serious risks that have surfaced in the vaccines’ wake—problems unheard of before the vaccines’ introduction?

With the rollout of mass varicella vaccination, shingles started cropping up to an unprecedented extent in both children and adults, eliminating boosting for adults and shifting downward the average age at which shingles occurs.

Varicella and rotavirus vaccines

The rationale for the varicella and rotavirus vaccines was dubious from the start. In the U.S. and other wealthy countries, varicella and rotavirus were nearly universal and mostly benign childhood infections; in those settings, the pre-vaccine impact of the two conditions was largely measured in terms of “healthcare costs, missed daycare, and loss of time from work for parents/guardians” rather than in terms of serious illness or mortality.

Childhood chickenpox infections served an important purpose for all, conferring lifelong immunity to infected children while boosting adult immunity to the related shingles (herpes zoster) virus. With the rollout of mass varicella vaccination, shingles started cropping up to an unprecedented extent in both children and adults, eliminating boosting for adults and shifting downward the average age at which shingles occurs. Vaccine waning also began increasing young adults’ risk for varicella outbreaks and complications later in life, presenting “perverse public health implications.” Meanwhile, the CDC and its local public health partners worked hard to conceal these unwanted chickenpox vaccine outcomes from the public.

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Rotavirus vaccines have had a similarly checkered history. Soon after their introduction in the U.S., reports emerged of a substantially increased risk in infants of an otherwise rare bowel complication called intussusception. The FDA knew about the problem during the prelicensing regulatory review process but ignored it. Although the agency subsequently withdrew its approval for one of the problematic rotavirus vaccines, it was not until after an estimated 500,000 children received at least one million doses. The FDA never explained the “precise mechanism” by which the discontinued vaccine caused intussusception.

Two rotavirus vaccines that display the same intussusception risks are still on the U.S. market. Both are contaminated with foreign DNA from porcine viruses capable of causing severe immunodeficiency in pigs. Had the presence of these “adventitious agents” been discovered prior to vaccine licensure, the FDA probably would have been forced to shelve the vaccines, yet they remain on the vaccine schedule to this day.

The speed with which the FDA gave them [HPV vaccines Gardasil and Gardasil-9] the go-ahead—despite obvious red flags regarding their safety—illustrates the insincerity of the agency’s assertions that its vaccine approval process is committed to minimizing risks.

HPV vaccines

The HPV vaccines Gardasil and Gardasil-9 (manufactured by Merck) represent perhaps an even more compelling case study of risk-laden vaccines that should have attracted strong up-front regulatory scrutiny—but didn’t. The speed with which the FDA gave them the go-ahead—despite obvious red flags regarding their safety—illustrates the insincerity of the agency’s assertions that its vaccine approval process is committed to minimizing risks.

The FDA not only gave the quadrivalent Gardasil a free pass but has repeatedly reapproved it and the nine-valent Gardasil-9 for wider use. (Gardasil-9 is a newer formulation that contains more than twice the amount of neurotoxic aluminum adjuvant as Gardasil.) In 2009, the FDA also okayed GlaxoSmithKline’s HPV vaccine, Cervarix, but Merck’s FDA-facilitated stranglehold on the market prompted the company to withdraw Cervarix from the U.S. in 2016. Merck is now aggressively expanding its Gardasil “franchise” into other countries, generating unprecedentedworldwide demand, while continuing to “rev up” U.S. sales.

Since 2006, the FDA’s Gardasil-related decisions have included:

  • 2006: Granting fast-tracked approval for the original quadrivalent Gardasil vaccine (girls and women aged 9 to 26 years)
  • 2009: Approving Gardasil’s use in boys and men (ages 9-26)
  • 2014: Approving Gardasil-9 (girls ages 9-26, boys ages 9-15)
  • 2015: Approving Gardasil-9 for boys ages 16-26
  • 2018: Approving Gardasil-9 for older women and men (ages 27-45)

An eight-month investigation by Slate identified numerous troubling aspects of the clinical trials that encouraged U.S. and European regulators to approve Gardasil. The Slate reporter also criticized regulators for allowing “unreliable methods to be used to test the vaccine’s safety.” These included Merck’s use of “a convoluted method” that made it difficult to objectively evaluate and report side effects; its failure to document “symptom severity, duration, outcome, or overall seriousness”; restriction of adverse event reporting to just 14 days following each injection; and reliance on the subjective opinion of clinical trial investigators regarding “whether or not to report any medical problem as an adverse event.” Not infrequently, clinical trial participants who shared complaints of debilitating symptoms with trial investigators were dismissed with the response, “This is not the kind of side effects we see with this vaccine.”

The author of the Slate investigation reported:

Experts I talked to were baffled by the way Merck handled safety data in its trials. According to…a professor…who studies side effects, letting investigators judge whether adverse events should be reported is “not a very safe method of doing things, because it allows bias to creep in.” …Of the short follow-up…,“It’s not going to pick up serious long-term issues, which is a pity. Presumably, the regulators believe that the vaccine is so safe that they don’t need to worry beyond 14 days.”

Two years after Gardasil’s initial approval, Judicial Watch pronounced it a “large-scale public health experiment.” Post-licensure studies carried out since then confirm that HPV vaccines have grave risks, including impaired fertilitydemyelinating diseasechronic limb paincirculatory abnormalities and autoimmune illness, to name just some of the disabilities reported in the aftermath of HPV vaccines’ introduction. Overall, the “rate of reported serious adverse reactions (including deaths) from HPV vaccination” is many times higher than the cervical cancer mortality rate.

Recent data suggest that HPV vaccines may be increasing cervical cancer risks.

In a February 2019 letter to the CDC, Children’s Health Defense Chairman Robert F. Kennedy, Jr. noted, “During Gardasil’s clinical trials, an extraordinary 49.5% of the subjects receiving Gardasil reported serious medical conditions within seven months of the start of the clinical trials. Because Merck did not use a true placebo in its clinical trials, its researchers were able to dismiss these injuries as sad coincidences.” A current civil case brought on behalf of a 24-year-old who has suffered from systemic autoimmune dysregulation since receiving her third Gardasil vaccine at age 16 alleges that Merck “committed fraud during its clinical trials and then failed to warn [vaccine recipients] about the high risks and meager benefits of the vaccine.” The trial’s legal team is benefiting from the support of an “A-team” of plaintiffs’ law firms and attorneys, including Kennedy, Jr.

Recent data suggest that HPV vaccines may be increasing cervical cancer risks. A 2017 study out of Australia—which has heavily promoted routine HPV vaccination since 2007—reported an increased risk of difficult-to-detect malignant cervical lesions among the HPV-vaccinated. In all countries where HPV vaccination coverage is high, including Australia, official cancer registries show “an increase in the incidence of invasive cervical cancer” in the vaccinated age groups. In England, “2016 national statistics showed a worrying and substantial increase in the rate of cervical cancer…at ages 20-24”—the first HPV-vaccinated cohort.

The proper decision would be to take HPV vaccines off the market, but the FDA and CDC continue to look the other way. Both agencies’ unwavering support for Gardasil has clearly helped Merck’s commercial bottom line, so much so that the CDC director at the time of Gardasil’s approval (Julie Gerberding) went on to be appointed president of Merck’s profitable vaccine division (worth $5 billion globally) in 2009. The agencies’ willingness to aggressively promote HPV vaccination despite its readily apparent dangers illustrates a “public health flimflam” of the first order. Before the U.S. introduction of HPV vaccination, a decades-long pattern of declining cervical cancer rates was already well underway, thanks to routine cervical cancer screening. HPV vaccines have never even been proven to prevent cervical cancer. In 2016, researchers admitted that they would be unable to ascertain HPV vaccines’ long-term efficacy for “at least another 15-20 years.”

Officials also seem to have little interest in modern evidence documenting many vaccines’ inability to provide the promised protection, even when vaccine coverage is widespread.

Pertussis-containing vaccines

Alongside their many misplaced claims about various vaccines’ rationale and safety record, the FDA and CDC—as echo chambers for the vaccine industry—also have misinformed the public about vaccine effectiveness. Back in 1899, doctor William Bailey (vaccination enthusiast and member of the State Board of Health in Louisville, Kentucky) was more honest, cautioning that “nothing is gained by claiming too much” about vaccine-induced immunity and stating that “the degree of immunity may vary with time and circumstance”—presaging the troublesome modern phenomena of vaccine failure and waning immunity. In the present day, officials are only too willing to “claim too much,” conveniently ignoring historical evidence that reductions in infectious disease had little to do with vaccines and far more to do with improvements in sanitation and nutrition. Officials also seem to have little interest in modern evidence documenting many vaccines’ inability to provide the promised protection, even when vaccine coverage is widespread.

The acellular version of pertussis (whooping cough)—a component of U.S. vaccines such as DTaP and Tdap—is one of the vaccines noted for its abysmal effectiveness. The vaccine is supposed to protect against the respiratory infection caused by Bordetella pertussis. Instead, according to recent studies, pertussis is making a “surprising” comeback; between 1990 and 2005, pertussis epidemics increased in the U.S. “in both size and frequency,” and over half of all cases occurred in highly vaccinated adolescents aged 10 to 20 years old. In fact, not only is pertussis at its highest level since the mid-1950s, but, according to CDC researchers, it is showing signs of being vaccine-resistant. The CDC researchers also note “substantial heterogeneity among vaccine recipients in terms of the durability of the protection they receive.”

… the researchers concluded in 2017 that all currently available evidence suggests that DTP vaccine may kill more children from other causes than it saves from diphtheria, tetanus or pertussis …

West Africa has used the DTP vaccine since the 1980s—formulated with a whole-cell pertussis component instead of acellular pertussis—and it has an even more horrifying safety and effectiveness record than its acellular counterparts. Research published in 2017 by a prestigious team of international scientists and led by vaccinology expert Dr. Peter Aaby found that DTP vaccination had a negative effect on child survival, with fivefold higher mortality in young DTP-vaccinated infants (ages three to five months) compared to as-yet-unvaccinated infants. When the researchers published results in 2018 for slightly older DTP-vaccinated children (ages six months to three years), they continued to observe more than double the risk of death as similarly situated unvaccinated children. Explaining that vaccines can increase susceptibility to other infections, the researchers concluded in 2017 that “all currently available evidence suggests that DTP vaccine may kill more children from other causes than it saves from diphtheria, tetanus or pertussis” and added in 2018 that “all studies of the introduction of DTP have found increased overall mortality.”

Learning from history

Efforts to counter the official vaccine narrative with evidence about negative consequences date back to the days of smallpox. A doctor practicing in the 1870s observed that smallpox mortality doubled (from roughly 7% to 15%) after adoption of smallpox vaccination. During an outbreak in 1871 and 1872, this doctor stated, faith in vaccination received a “rude…shock” when “[e]very country in Europe was invaded with a severity greater than had ever been witnessed during the three preceding centuries.” The doctor also noted that “many vaccinated persons in almost every place were attacked by small-pox before any unvaccinated persons took the disease.” In this individual’s estimation, these facts were “sufficient to overthrow the entire theory of the protective efficacy of vaccination.”

In the present era, federal agencies continue to tout difficult-to-justify but money-spinning vaccines as beneficial, even in the face of substantial evidence to the contrary. Now, more than ever, it is important to illuminate the risks and downsides that public health agencies do not want us to know about.

Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. 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.

Help Support Collective Evolution

The demand for Collective Evolution's content is bigger than ever, except ad agencies and social media keep cutting our revenues. This is making it hard for us to continue.

In order to stay truly independent, we need your help. We are not going to put up paywalls on this website, as we want to get our info out far and wide. For as little as $3 a month, you can help keep CE alive!

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