Anti Vaccine campaign
Robert F. Kennedy Jr. is continuing his personal crusade against Big Pharma and Big Government collusion, authoring a hard-hitting article explaining that the government are withholding information from the public about vaccines – and covering up vaccine deaths – in order to protect pharmaceutical companies.
Vaccine scientists and the public health community cautiously and occasionally will admit that vaccines can cause adverse reactions just like “any other medication or biological product.” Although experts are less willing to openly disclose the fact that adverse reactions can and do include death, one has only to look at reports to the U.S. Vaccine Adverse Event Reporting System (VAERS) to see that mortality is a possible outcome.
From 1990 through 2010, for example, VAERS received 1,881 reports of infant deaths following vaccination, representing 4.8% of the adverse events reported for infants over the 20-year period.
Moreover, analysts acknowledge that VAERS, as a passive surveillance system, is subject to substantial underreporting. A federal government report from 2010 affirms that VAERS captures only about 1% of vaccine adverse reports.
Guided by this tool, public health teams examined temporal criteria and possible alternative explanations to determine whether the relationship of an AEFI to vaccine administration was “very likely/certain,” “probable,” “possible,” “unlikely,” “unrelated,” or “unclassifiable.”
In 2013, the WHO’s Global Advisory Committee on Vaccine Safety discarded the prior tool, ostensibly because users “sometimes [found it] difficult to differentiate between ‘probable,’ ‘possible,’ and ‘unlikely’ categories.” The WHO enlisted vaccine experts to develop a “simpler” algorithm that would be more readily “applicable” to vaccines. The resulting four-category system now invites public health teams to classify an AEFI as either “consistent,” “inconsistent,” or “indeterminate” with a vaccine-related causal association or as “unclassifiable.”
Despite the patina of logic suggested by the use of an algorithm, “the final outcome of the case investigation depends on the personal judgment of the assessor” [emphasis added], especially (according to the tool’s proponents) when the process “yields answers that are both consistent and inconsistent with a causal association to immunization.”
In a 2017 letter in the Indian Journal of Medical Ethics, Drs. Jacob Puliyel (an India-based pediatrician and member of India’s National Technical Advisory Group on Immunization) and Anant Phadke (an executive member of the All India Drug Action Network) raise important questions about the revised tool.
They describe an Orwellian Catch-22 situation wherein it is nearly impossible to categorize post-vaccine deaths as vaccine-related. This is because the revised algorithm does not allow users to classify an AEFI as “consistent with causal association with vaccine” unless there is evidence showing that the vaccine caused a statistically significant increase in deaths during Phase III clinical trials.
By definition, however, any vaccine not found to “retain safety” in Phase III trials cannot proceed to Phase IV (licensure and post-marketing surveillance). The result of the algorithm’s convoluted requirements is that any deaths that occur post-licensure become “coincidental” or “unclassifiable.”
Drs. Puliyel and Phadke describe what happened in India when the country’s National AEFI committee assessed 132 serious AEFI cases reported between 2012 and 2016, including 54 infant deaths that followed administration of a pentavalent all-in-one vaccine intended to protect recipients against diphtheria, tetanus, pertussis, hepatitis B, and Haemophilus influenzae type b infections. For babies who survived hospitalization, the committee classified three-fifths (47/78) of the AEFI as causally related to vaccines (with 47% of the incidents viewed as “product-related” and 13% as “error-related”), but they rated nearly all (52/54) of the deaths as either coincidental (54%) or unclassifiable (43%) despite mounting evidence that pentavalent and hexavalent vaccines are increasing the risk of sudden unexpected death in infants.
…doctors who “naïvely” accept biased reports on vaccine safety “are losing the trust of the public and in the process…endangering public health.”
The absurdity and negligence inherent in the ultimately subjective WHO checklist have not escaped the attention of others in India and beyond. In a series of comments published in the journal Vaccine in response to the 2013 publication of the revised tool, commenters issued the following scathing remarks:
- “Even if a healthy child dies within minutes following vaccination and there is no alternate explanation for the AEFI, even then the powers that be could easily declare that death as coincidental and not due to the vaccine, thanks to the new AEFI. This is dangerous ‘science’.”
- “Amongst the 20 items of their checklist, no less than 15 (75%) are devoted to refute a vaccine-induced causality [emphasis in original]…. After all and as the authors confess with an astonishing ingenuousness, the main point is to ‘maintain public confidence in immunization programs.’”
- “People understand that there are no true coincidences—only events that have been made to appear to be coincidental by either a genuine lack of understand[ing] of the overall facts leading to the ‘coincidence’ reported or by the deliberate suppression of the facts, including when…AEFIs that result in death are made to ‘disappear.’”
- “It seems that huge business in [the] vaccine industry is affecting [the] science of vaccines and we are developing various ways to promote the business at the cost of human lives. …Going for a less sensitive tool for safety concerns is not only illogical but risky for the children of the world.”
Unfortunately, many vaccine proponents appear to be more concerned with forestalling “misconceptions” and “erroneous conclusions about cause and effect” than they are about preventing and identifying adverse events following vaccination. The result, as Dr. Puliyel argues, is that doctors who “naïvely” accept biased reports on vaccine safety “are losing the trust of the public and in the process…endangering public health.”
The chemicals once seemed near magical, able to repel water, oil and stains.
By the 1970s, DuPont and 3M had used them to develop Teflon and Scotchgard, and they slipped into an array of everyday products, from gum wrappers to sofas to frying pans to carpets. Known as perfluoroalkyl substances, or PFAS, they were a boon to the military, too, which used them in foam that snuffed out explosive oil and fuel fires.
It’s long been known that, in certain concentrations, the compounds could be dangerous if they got into water or if people breathed dust or ate food that contained them. Tests showed they accumulated in the blood of chemical factory workers and residents living nearby, and studies linked some of the chemicals to cancers and birth defects.
More from ProPublica:
Now two new analyses of drinking water data and the science used to analyze it make clear the Environmental Protection Agency and the Department of Defense have downplayed the public threat posed by these chemicals. Far more people have likely been exposed to dangerous levels of them than has previously been reported because contamination from them is more widespread than has ever been officially acknowledged.
Moreover, ProPublica has found, the government’s understatement of the threat appears to be no accident.
The EPA and the Department of Defense calibrated water tests to exclude some harmful levels of contamination and only register especially high concentrations of chemicals, according to the vice president of one testing company. Several prominent scientists told ProPublica the DOD chose to use tests that would identify only a handful of chemicals rather than more advanced tests that the agencies’ own scientists had helped develop which could potentially identify the presence of hundreds of additional compounds.
The first analysis, contained in an EPA contractor’s PowerPoint presentation, shows that one chemical — the PFAS most understood to cause harm — is 24 times more prevalent in public drinking water than the EPA has reported. Based on this, the Environmental Working Group, an advocacy organization whose scientists have studied PFAS pollution, has estimated that as many as 110 million Americans are now at risk of being exposed to PFAS chemicals.
In the second analysis, ProPublica compared how the military checks for and measures PFAS-related contamination to what’s identified by more advanced tests. We found that the military relied on tests which are not capable of detecting all the PFAS chemicals it believed to be present. Even then, it underreported its results, sharing only a small part if its data. We also found that the military’s own research programs had retested several of those defense sites using more advanced testing technology and identified significantly more pollution than what the military reported to Congress.
Even before the troubling new information about PFAS chemicals emerged, the government had acknowledged problems relating to them were spreading. Past EPA water testing, however incomplete, identified drinking water contamination across 33 states that Harvard researchers estimated affected some 6 million people. The military suspected drinking water at more than 660 U.S. defense sites where firefighting foam was used could be contaminated; earlier this year, it announced it had confirmed contamination in 36 drinking water systems and in 90 groundwater sites on or near its facilities.
The new analyses suggest these findings likely represent just a fraction of the true number of people and drinking water systems affected.
In written responses to questions, the EPA did not directly address whether it had understated contamination from PFAS chemicals. The agency said it had confidence in its current testing procedures and had set detection limits at appropriate levels. It also stated that it is taking steps towards regulating some PFAS compounds and registering them as “hazardous substances,” a classification that triggers additional oversight under waste and pollution laws.
The agency will “take concrete actions to ensure PFAS is thoroughly addressed and all Americans have access to clean and safe drinking water,” then-EPA Administrator Scott Pruitt, who recently resigned, said in the written statement to ProPublica in May.
The Department of Defense also responded to questions in writing, defending its testing methods as the best available and calling it difficult to fully assess risks from PFAS because the EPA has not regulated these chemicals. A DOD spokeswoman said the Pentagon’s research group has a program underway aimed at enhancing the test methods and detecting more PFAS compounds, but suggested that no alternatives were ready for use. She did not answer questions about why the agency reported contamination levels for only two chemicals to Congress when it would have had data on many more, stating only that the Pentagon “is committed to protecting human health and the environment.”
Environmental experts aren’t convinced.
“Widespread contamination may be harming the health of millions or even tens of millions of Americans and the government is intentionally covering up some of the evidence,” said Erik Olson, a senior director for health, food and agriculture initiatives at the Natural Resources Defense Council, in an interview. The EPA and Defense Department “have done all they can to sort of drag their feet and avoid meaningful regulatory action in making significant investment in cleanups.”
In May, a Politico report revealed that the EPA and the White House, along with the Defense Department, had pressured a division of the Centers for Disease Control and Prevention to withhold a health study expected to warn that people exposed to PFAS chemicals face greater health risks than were previously understood. That report was quietly released in mid-June and, indeed, estimated safe levels of exposure are seven to 10 times smaller than what the EPA has said.
Such a determination could spur stricter limits on exposure than the EPA appears to have considered. Paired with an emerging realization that testing by the EPA and DOD hasn’t captured the true extent of contamination, the government could be forced to reconceive its approach to these compounds, said David Sedlak, the director of the Institute for Environmental Science and Engineering at the University of California, Berkeley, who helped develop one of the most advanced commercial tests for PFAS substances.
“Not talking about it isn’t going to make the problem go away,” Sedlak said. “And because these compounds are forever — they aren’t going to degrade on their own — eventually there is going to be a day of reckoning.”
Click Here for more of this detailed report by
The owner of the Radhakrishna restaurant and Golden Chariot restaurant opposite to Stopper Shop, S.V. Road, Andheri (West), Mumbai….Mr. Harish Shetty had diabetes, High Blood pressure and Uric acid problem. He changed his diet and got healthy without taking medicines. Inspired by his healthy eating which relieved him of his ailments, he started a restaurant called “Aharveda”
Address – Viral Apartments, Opposite Shoppers Stop, S. V. Road, Andheri West, Mumbai , Tel – 40722211/40722212 Time – 12 pm to 8 pm. No food served after 8 pm
Website – https://aharveda.com/
They also have lunch and dinner delivered at door step services Monday to Saturday.
What’s special about Aharveda?
An Aharveda diet does not use oil, ghee, dairy products or sugar, yet it isn’t about eating boiled vegetables for lunch and dinner.
In fact, you could be tucking into a mouth-watering avial or vegetable makhanwala, and gajar halwa. Surprised?
Enjoy a raita made out of peanut curd instead of dairy yoghurt, aloo parathas with gluten-free rajgira flour instead of wheat, and pulao with wari. And no more saying ‘no’ to shrikhand or payasam.
Palm jaggery, dates and figs make your desserts guilt-free.
Harish Shetty in conversation with Deepti Bhatnagar at Aharveda.
And,,, and interview with the inimitable Cyrus Broacha
Charitybeds.com is an initiative by a group of young individuals who are disturbed by the discrimination faced by the under privileged at private hospitals in the city. We are a team of young professionals across various industries who feel there is a lack of accurate information and awareness about what the law stipulates and the ground reality. Our aim is to also provide information to other charitable institutions and organisations working with the underprivileged, on where they can go for free medical care.
Private hospitals in Delhi have been allotted prime land for Rs 1 an acre as against a market value of 20 – 80 crores an acre, in return for this, the government made it compulsory for them to offer 10 % beds with ALL MEDICINES & TESTS INCLUDED and 25% of all OPD- consultation with doctors to be free. Charitybeds, helps all under privileged people achieve healthcare even when they have no money. A lot of private hospitals have joined hands with us and are actually working with us to fulfil their social responsibility. We do not charge anything, our only role is to facilitate and save lives, wherever we can.
We help patients when someone calls us, we go to government hospitals and pick up patients from there, we help people reaching private hospitals directly. We help people who have BPL ( Below the poverty line) cards and people who do not have any card as they are not aware because they are so poor.
Charitybeds.com works along with Ritinjali, a volunteer-based organization that is firmly rooted in its philosophy of providing a helping hand wherever needed, to anticipate social and community issues and to promote responsible citizenship. Mr. Arun Kapur, Founder,Ritinjali, is a key partner with Charitybeds.com. His team includes Mr. Naveen Pabla and Mr. Ashish Alex have supported us in creating Charitybeds.com. Charitybeds.com was born out of the vision of Mr Kapil Chopra, President,The Oberoi Group. His leadership has brought the initiative together and it is his passion and commitment to the cause that is the key driving force behind this initiative.
Mr. Lalit Bhatia one of the key people heading the initiative has been a social worker for over 25 years and offers his expertise and knowledge in multiple social welfare domains.He works closely with senior citizen welfare schemes and works full time with Charitybeds.com. They visit hospitals daily, creating awareness and till date have distributed over 30,000 flyers and run a poster campaign along with awareness camps in every major hospitals. Gagan works along with Mr Bhatia to ensure that we can even help more people, Gagan is an aspiring filmmaker and a photographer who is passionate about social causes and you can also check out his patient testimonial videos on the website. In addition to this,we have volunteers who come and work with us on a daily basis.You will find our people in all hospitals across Delhi everyday from 10 AM to 5 PM.
We need your help,call us and volunteer a day with us, spread the word, tell friends, tell journalists, post on Facebook, let us get the message out. Everyday, inspite of all our efforts, only 400 out of 653 free beds get utilised, everyday,someone dies because they did not have money to buy medicines or get medical care. We are racing against time, help us to reach more people. It is the least we can do for this country. As of now, we operate only in Delhi but patients can come for any part of India and seek our assistance. We soon plan to be in Mumbai where most of the trusts which run hospitals actually do not support any free healthcare inspire of sitting on government land worth crores.
If you would like to contribute for the cause, please call Lalit Bhatia 99990 71842 or Gagan Bharti 7838348237 we need posters and flyers all the time.
This video is a talk by Ms. Zenobia Khodaiji 13 Feb 2016. Topic “Body & Cell Regeneration- Removing Negativity From Life”. This is part of the HELP Talk series at HELP,Health Education Library for People, the worlds largest free patient education library www.healthlibrary.com
“The desire to take medicine is perhaps the greatest feature which distinguishes man from animals.” –– Sir William Osler
“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…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” — 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 20th century.
“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 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 Big Pharma’s drugs, especially its psycho-pharmaceutical drugs. Big Pharma has found that the promotion and de-stigmatization of so-called “mental illnesses of unknown etiology” is a great tool for marketing their drugs.
Recently Alzheimer’s support groups all around the nation have been marketing a documentary about country singer Glen Campbell who has recently been diagnosed 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, addictive, and very neurotoxic drugs like cocaine and alcohol. And, just like so many other hard-living celebrities like the (now cured) dementia victim Kris Kristofferson and the suicidal and early dementia victim Robin Williams. All three celebrities were known to have received prescriptions for legal neurotoxic brain-altering drugs, adding to the burdens that their failing brains, livers and psyches had to endure. It is highly likely that all three of them were also on statins and were up-to-date on their mercury and aluminum-containing vaccinations.
It is an established fact that Alzheimer’s disease can only be definitively diagnosed at a post-mortem examination of the cerebral cortex, something that dementia patients are almost never subjected to. Because of the rarity of coroners doing autopsies on dementia patients, we have to question the accuracy of the diagnoses of, for example, the still living Glen Campbell, Kris Kristofferson and our own memory-impaired spouses, aunts, uncles, grandmas and grandpas, especially since so many of them have been on neurotoxic substances such as those mentioned in this article.
And we also have to question the motivations of the Big Pharma corporations that financially underwrite patient support groups like the Alzheimer’s Association. AND, equally importantly, given the total lack of recognition of the reality of drug-induced dementia, we have to question to oft-cited assertion that 2/3 of all dementia cases are because of Alzheimer’s disease (of unknown cause).
Are the Alzheimer’s, Autism and Autoimmune Epidemics Actually Iatrogenic, Drug-Induced Epidemics?
Synchronous with the recent large increases in 1) childhood and adult neurotoxic aluminum-adjuvanted vaccinations, 2) the use of neurotoxic psychotropic drugs, 3) the use of statin drugs (cholesterol-lowering drugs) known to cause memory-impairment, and 4) the ingestion of a variety of neurotoxic food additives, there has been a large parallel increase in A) the incidence of chronic autoimmune disorders, especially in childhood, B)the incidence of autistic spectrum disorders, C) “mental illnesses of unknown origin” and D) dementia.
Each of those 4 root causes and the 4 neurological disorders that are closely correlated with them are admittedly multifactorial realities. But the important lesson is that they are also preventable. However, due to clever marketing by Big Pharma and the studied ignorance of Big Medicine and the refusal of Big Media to allow scholars to talk about the connections, “walks for the cure” and drug treatment is what is emphasized rather that prevention.
So what we need to ask – and then demand – is 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 the equally over-prescribed immunotoxic and neurotoxic vaccines (that often contain either of the heavy metals aluminum and mercury) and some of the neurodegenerative disorders that supposedly “have no known cause”? Could the disabling American epidemic of autoimmune disorders, psychiatric disorders, autism spectrum disorders, etc (all supposedly of unknown origin) be found to have recognizable iatrogenic root causes and therefore be preventable? Psychiatrist and scholar Grace E. Jackson has the answers in her seminal (and black-listed) book
“Drug-Induced Dementia: A Perfect Crime”.
These are extremely important issues, especially in the case of the dementia epidemic, because the Alzheimer’s patient support groups seem to be unaware of the fact that many psychiatric drugs are known to irreversibly damage brain cells (partly by poisoning their mitochondria, the microscopic hearts and lungs of every cell) and therefore would be expected to cause a variety of other neurological and mental health disorders. (See more info on drugs and mitochondria below.
One of the big problems in America’s corporate-controlled culture, corporate-controlled government, corporate-controlled medical industries and corporate-controlled media is that the giant multinational (especially Big Pharma) corporations are in the business of developing and marketing known mitochondrial toxins with no oversight from regulatory agencies. These businesses obscure the fact that there ARE known causes for the disorders and that they are preventable. The unproven claims expressed in the TV commercials and medical journals advertising the newest drug-of-the-month are often later exposed as plain snake oil propaganda.
It should be a concern for everyone that some Alzheimer’s support groups are actually front groups for the pharmaceutical industry that profit handsomely from the handful of virtually useless drugs such as Aricept, Exelon, Namenda, Hexalon, and Razadyne.
Prescription Drug-Induced and Vaccine-Induced Mitochondrial Disorders
Acquired mitochondrial disorders (as opposed to the rare primary mitochondrial disorders like muscular dystrophy) can be caused by commonly prescribed drugs. They are difficult to diagnose and are generally poorly understood by most healthcare practitioners. When I went to medical school, none of my professors knew anything about the lethal effects that many synthetic drugs and vaccines do to the mitochondria of average brain or body cells. The science of the mitochondria was in its infancy.
A lot of mitochondrial research has been done since then, especially starting in the 1990s,and that research 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 whose drug are the culprits. Big Pharma has tremendous control over the medical education of most health care providers, and they spoon-feed pro-drug and pro-vaccine propaganda to undiscerning “healthcare” journalists, which is where many physicians and patients get their health information.
An Honest Patient Guide for Dementia Patients (from Harvard)
I was pleasantly surprised recently to find a reasonably honest guide for dementia patients on a Harvard University website.
The entire guide can be accessed at
The information at that site stated that there were over 50 conditions that could cause or mimic early dementia symptoms. What medical practitioner in our double-booked clinic environment has the time to thoroughly rule out the 50 root causes of dementia symptoms when confronted with a patient with memory loss? It’s simpler to just diagnose every case of dementia as another case of Alzheimers! Who will ever dispute such an authoritative-sounding diagnosis? Certainly not those who want to keep dementia from being recognized as a potentially iatrogenic disorder (doctor or treatment-caused disorder).
I have often said to my patients and seminar participants: “it takes only 2 minutes to write a prescription, but it takes 20 minutes to not write a prescription”. In the current for-profit clinic culture, time is money and very few physicians are ever given the “luxury” of spending sufficient time listening carefully to their patients. (In defense of the physicians that I know, they are not happy about these realities but feel powerless to do anything about it.)
It is so tempting for us physicians to use the popularized, but rather squishy label of Alzheimer’s dementia rather than to educate ourselves about the possibility of drug-induced, vaccine-induced or malnutrition-related dementia. But what is so important is that many of the 50+ conditions are preventable or reversible, which will be therapeutic only if the real root causes are identified before permanent brain damage occurs. Just one example was the subject of the book “Lipitor: Thief of Memory” written by former astronaut and flight surgeon Duane Graveline, M.D., M.P.H
(for more information go to https://www.spacedoc.com/articles/lipitor-thief-of-memory.)
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 and cell carcasses or scars. In imaging scans, brain shrinkage is usually first noticeable in the hippocampus, which plays a central role in memory function.”
The FDA Does Not Require Big Pharma to Test its New Drugs or Vaccines for Mitochondrial Toxicity
But even the Harvard guide inexplicably fails to mention known mitochondrial toxins such as statins, metformin, Depakote, general anesthetics, fluoroquinolone antibiotics (like Cipro), fluorinated psychotropic drugs (like many of the SSRIs and the so-called antipsychotics).
And Big Food corporations are guilty of feeding us neurotoxins also.
For example, when the ubiquitous synthetic food, soft drink and chewing gum sweetener NutraSweet (aspartame) reaches 86 degrees (whether in our 98.6 degree bodies or in some MidEast desert (as was true for many American soldiers who developed Gulf War Syndrome) every molecule releases a molecule of the excitotoxic amino acids phenylalanine and aspartic acid and one molecule of the cellular toxin methanol (wood alcohol). Methanol then rapidly metabolizes into the known mitochondrial poison formaldehyde (embalming fluid), which is a serious cellular and mitochondrial toxin.
The chlorinated artificial sweetener Splenda, which was initially developed as a neurotoxic pesticide, is in an uncountable variety of foods as well.
These examples are only some of the synthetic chemicals in medicines, vaccines and processed foods that are capable of causing mitochondrial damage in brain and body cells – with memory loss, confusion and cognitive dysfunction, all early symptoms of dementia.
It is a tragedy for reversible and preventable drug- or vaccine-induced dementias (or any of the many neurodegenerative disorders) to be mis-diagnosed as Alzheimer’s disease (or neurological disorder) “of unknown cause” because if the root causes are not recognized preventive care will not be offered. And then, what may be worse, those patients might be placed on costly, potentially toxic and often useless medications that have not been tested for their own potential mitochondrial toxicities. (Tragically, the American pharmaceutical industry is not required by the FDA to test its drugs for mitochondrial toxicity, thus leaving physicians and their drug-consuming patients in the dark as far as safety of those medications is concerned.)
There is much more in the basic neuroscience literature proving the connections between drugs and vaccines and neurodevelopmental disorders. Those basic neuroscience researchers that do not have conflicts of interest with Big Pharma and Big Medicine should be listened to. Those authors with monetary or professional conflicts of interest should be regarded with suspicion.
Don’t expect Big Pharma to respond to such unwelcome revelations as mentioned above. Don’t expect Big Medicine to acknowledge the existence of iatrogenic illnesses or to offer apologies.
Do, however, expect denials, dismissals, distractions, delays and ad hominem attacks against the whistle-blowers rather than honest mea culpas.
So it must be up to the consumers of potentially toxic substances to do the research themselves, for those substances may not show symptoms until a tipping point is reached when their livers can no longer detoxify the cocktail of poisons that are presented to it).
Professor of Medicine Oliver Wendell Holmes once said: “If all the medicine in the world were thrown into the sea, it would be bad for the fish, but good for humanity.”
Dr Kohls has spent many years researching the powerful, obscenely profitable and therefore easily corrupted pharmaceutical industry and the many false claims that their lobbyists, think tanks and co-opted opinion leaders in the media have been making. He knows many families whose lives have been devastated by psychiatric drug and vaccine injuries, including the post-vaccination regressive autism that unequivocally began following routine well-baby or well-child vaccinations. He takes seriously the precepts of the Hippocratic Oath that he took when he received his medical degree. That oath says that physicians should above all do no harm to their patients and thus, when there is evidence of potential harm from a prescription drug, vaccine or procedure, physicians should hesitate in doing that harmful treatment until a thorough, unbiased re-evaluation is done.
Tragically, there has been a proliferation of big medical corporations (for-profit health insurance companies, for-profit clinics, for-profit hospitals, etc) and the secretive, often above-the-law multinational pharmaceutical corporations that regularly use corrupted science to “prove” the safety and efficacy of their obscenely profitable drugs. They employ thousands of workers but mainly work for the economic benefit of their shareholders and not vulnerable patients.
Dr Kohls practiced holistic mental health care for the last decade of his family practice career. He now writes a weekly column for the Reader Weekly, an alternative newsweekly published in Duluth, Minnesota, USA. Many of his Duty to Warn columns have been archived at
AIR WICK ESSENTIAL OILS
But how is this scent really achieved?
A TINA.org reader wrote in:
It is very unlikely that there is any real lavender in this product, as they have supposed customers choose between its scent and “real lavender.” Even if it did contain real lavender, it is highly doubtful that they would be counting the number of flowers in every bottle.
TINA.org asked Air Wick how it arrived at over 80 lavender flowers per bottle. We have yet to get a response.
But what we found when we looked up a lavender-scented essential oil on Air Wick’s website is that the first ingredient in the product (and thus the most predominant) is not “over 80 lavender flowers” but fragrance. The Environmental Working Group, a nonprofit that examines ingredients in consumer goods, has referred to the ingredient fragrance as “a black box for hundreds of chemicals in thousands of everyday products.” This is because fragrance is one of two ingredients on a product label that itself can be comprised of hundreds of natural and synthetic ingredients. The other is “flavor.” Under U.S. regulations, companies are allowed to simply list “fragrance” or “flavor” to protect trade secrets.
But we did some digging and, according to a “safety data sheet” for the lavender-scented essential oil, here’s some of what appears to go into Air Wick’s fragrance formula (in descending order of predominance):
- Dipropylene glycol monomethyl ether (aka dipropylene glycol methyl ether), a chemical that a federal database describes as “a colorless liquid with a weak odor.” (Perfect for an air freshener, right?)
- Linalyl acetate, which the database says is “isolated from numerous plants and essential oils, e.g. clary sage, lavender, lemon etc.” (Apparently, this is where Air Wick’s product gets its lavender smell.)
- 1,1-Dimethyl-2-phenylethyl acetate
- Hexyl salicylate
Perhaps not what you would expect from a product advertised in the commercial as “infused with 100% natural essential oils.”
Essential oils are appealing to consumers because the source is natural. However, the FDA warns:
Sometimes people think that if an “essential oil” or other ingredient comes from a plant, it must be safe. But many plants contain materials that are toxic, irritating, or likely to cause allergic reactions when applied to the skin.
Find more of our coverage on essential oils, which are prevalent in the MLM industry, here.