I posted this in response to the “I Am Adam Lanza’s Mother” article that has been making the Internet rounds. I am not literally the Connecticut shooter’s doctor. That is a metaphor. I have dealt with people like the shooter; I speak with experience. In this time of horrific tragedy, let your voice be heard by decision makers: http://tinyurl.com/PsychDrugsKill. Please share this link with all your circles of influence. REL
I have treated “Adam Lanza” — male and female, young and old, for decades.
I am a Child, Adolescent and Adult Psychiatrist. I did my psychiatric residency at Lincoln Hospital and, along with my child psychology residency, also at St. Luke’s Hospital of Columbia University.
I have worked with Autistic people of all ages, the Asberger’s Syndrome people, Schrizophrenic people, BiPolar people, Multiple Personality Disorder people, OCD, ADD, ADHD, and pretty much every other type of labeled person in my 42+ year career since graduating from the Albert Einstein College of Medicine in New York City.
And I have never written a prescription for a psychiatric drug. Or any other type of drug, for that matter.
I have, while serving as the Acting Director for a Child and Adolescent Psychiatric Ward of a large hospital not very far from Newtown, CT, looked at the drugged, disoriented, drooling and dangerous children in my care ranging from age 4 to 16 and take ALL of them off all psychiatric medication, weaning them carefully, of course, because I simply could not tell what we were dealing with other than drug-damaged brains and bodies of the young and very young kids I had under my care.
The nurses told me I could not do that because they could not contain the children. I asked them how they knew that since the children who were violent, homicidal and suicidal were ALL on drugs known to make them violent, homicidal and suicidal.
They told me that I could not do that and that they would go to the union to prevent me from taking the kids off their meds. I replied that the meds were not the kids’ meds. They were the staff’s meds since they kept the staff comfortable and feeling safe.
They went to the Union. I had my physician’s license in CT, a Union Card that trumped theirs.
The 4 year old on 11 different psychiatric medications who was toe walking (a sign of neurological damage in a 4 year old) and who wanted to die stopped drooling and spinning around in circles when she came off the meds.
I was the first person to ask he why she had plunged a knife into Mommy’s boyfriend’s leg when he was asleep. She told me “He was hurting me down there [pointing to her vagina] every night and Mommy would not stop him”. When the event occurred, she was medicated without a single person taking a moment to ask why the act had taken place.
You see, I am old enough to have learned my craft and art BEFORE the advent of untested, highly profitable, and totally unconscionable psychiatric drugs. I read the literature on these neurological poisons and saw that the long terms studies were absent, that the pediatric studies were absent and that the advertising-supported “impartial” journals were nothing more than paper prostitutes all dressed up in paper dresses and glossy ads.
I watched in horror as younger and younger children were placed on stronger and stronger drugs for less and less indication (although, admittedly, in my mind there is no justification for the use of any psychiatric drug).
I learned orthomolecular medicine and psychiatry. That works. I learned how to listen and move people toward emotional health. That works too. I learned how to employ NeuroBioFeedback to teach the brain how to regulate itself and the body in harmony with its capacity and needs. That works fantastically well. I learned how to use frequency medicine, homeopathy, herbal medicine, intravenous nutrition and a variety of other modalities which actually support healing. They work.
I learned how to use nutrition, diet and detoxification, for which I studied Environmental Medicine. That works.
What does not work is drugging the brain with toxins which create the very symptoms for which the drugs are given in the first place.
I have met and held “Adam Lanza’s” mother in my arms as she wept in fear and exhausted despair. And I have held her in my arms as she wept for the joy of having her child clear eyed and of sound mind not in moments of quick hope, but continually and consistently.
I have held “Adam Lanza’s” mother’s hand in court as we pressured his school to give him the education he needed, not the one that they made money on from destructive State subsidies for the correct diagnosis and another drugged kid.
I have sat with “Adam’s” brothers and sisters helping them to undo the trauma that Adam-on-drugs has brought to their lives.
“Adam Lanza” and I have spent hours together as he climbed out of the pit of his own psychosis, without drugs, confinement or violence, but not necessarily smoothly, either.
And I have attended the funeral of more than 1 “Adam Lanza” whose family pressured his mom, or whose divorced parent pressured the custodial parent through the Court, to put “Adam” on drugs – and then did not even have the good grace or decency to accept responsibility for his death.
We know of absolutely no chemical imbalance to account for mental and emotional illness. We know that genes are disrupted so function is distorted by a host of causes, chief among which are heavy metals like mercury and industrial poisons like formaldehyde, fluoride and foreign DNA and proteins which call forth an auto immune reaction and cause neurological disruption.
This is a type of expression of a larger cause of disability I have called “Genome Disruption Syndrome” or GDS (www.GDS-Therapy.com). It, not a psuedo-science “genetic drift”, accounts for the changes in the human genome which are linked to increased cancer rates, autism, increased diabetes rates and the other chronic, degenerative diseases which were virtually unknown in our grandparents and parents childhoods. The genome is the same. The genomic disruption is by no means the same.
Adam was, according to his uncle, being “treated” with Fantapt, a novel, and highly dangerous anti-psychotic previously rejected by the FDA for its high side effect profile, including aggression and psychosis.*
But he was also vaccinated. So this Adam Lanza was toxic with thimerosol (49.6% mercury by weight), formaldehyde, fluoride, MSG, foreign DNA, diploid cells, foreign protein, Polysorbate 80 (or “TWEEN”) and other systemic toxins injected into his body regardless of their toxicity and regardless of his ability to remove them from his body.
So this Adam was neurotoxic — a victim of Genome Disruption.
His mother, I must also presume, had no intent to harm him when she allowed his genome to be repeatedly overwhelmed with unnecessary and dangerous vaccines and then, similarly, with dangerous and unnecessary psychiatric medications. No, I am sure that she followed the perhaps-well-intentioned advice of experts who themselves have suspended their capacity to evaluate data and instead rely on the herd’s belief that since it is said so often, the safety and efficacy of the drugs and vaccines purveyed so beautifully in the journals and ads, seminars and trainings (complete with pizza and salad during a busy lunch in a windowless conference room in the clinic or hospital) must be safe and effective.
They are neither and the “Adam Lanza’s” and their mothers, sisters, brothers, fathers, neighbors and, today, his grieving neighbors in Newton, CT. can testify to that.
There is a time to say NO. That time has arrived. No to psychiatric drugs. There is ALWAYS a better way. More than half of the people who kill themselves are on psychiatric drugs.
No to vaccines. There could not be a worse way. Virtually every modern outbreak and epidemic takes place in the fully vaccinated, to which the vaccine pusher’s retort is, “Well, give people more vaccine doses since 2 (or 3, or 4 or more) did not work. Call them boosters!” I call them Genome Disruption.
No to GMOs which are likewise altering our very genome.
Psychiatric drugs kill both those who take them and those they turn on.
They are unnecessary and dangerous, but oh, so profitable.
All of our children are Adam Lanzas; all of them are his victims.
Yours in health and freedom, Dr. Rima
Rima E. Laibow, MD
Natural Solutions Foundation
PS: This is what General Bert Stubblebine (US Army ret.), my husband and the President of our Foundation, had to say:
“Our hearts reach out to all those who suffer at the hands of senseless violence, around the world. It must stop! It is urgent that you share this message with your entire circle of influence. Send them to Dr. Rima’s powerful message about Genome Disruption and the mass killing tragedies that mar our claim to civilized status. Dr. Rima Truth Reports bring you the immediate information you need to meet the challenges of the crises of crony corporatism, to protect yourself and family. Send all your circles of influence to Dr. Rima’s powerful message about Genome Disruption and the mass killing tragedies that mar our claim to civilized status. Send them here: http://tinyurl.com/PsychDrugsKill.” General Bert
Note: These videos and essay were written in direct response to the brave woman who authored “I am Adam Lanza’s Mother” about her experience with a similar child. Just as she is not literally Adam Lanza’s mother, so I am not claiming to be the physician who treated Adam Lanza. Readers are invited to understand that as a Child, Adolescent and Adult Psychiatrist I have treated many patients like Adam Lanza but never met him before the tragic deaths.
Natural Solutions Foundation
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THE END OF THE VACCINE MYTH
What I prefer to refer to as the “Advanced Health Care Physicians” — the doctors who went beyond their medical school indoctrination and found their way to become real healers — have warned people about the dangers of vaccination literally since the founding of that branch of pseudo-science.
For too long the voices of the good doctors have been drowned out by the persistent pro-vax propaganda from the drug-pushers and their crony cohorts in the CDC and the rest of the medical mega-biz establishment. Any doctors who courageously told the truth about the foreseeable harm to children from the uninsurable risk of vaccination have been viciously attacked by paid hacks for the biggest of the big biz: the Illness Control Industry.
Before I show you how the Vaccine Myth is now exposed as the bad science it is, you need to understand how desperate the medical establishment has become, when it comes to protecting the cash-cow that vaccine has become, since the days of con-man Jenner and his “Cow Pox” lies.
Witness the persecution of Dr. Andrew Wakefield, a well-respected British physician with impeccable credentials. In 1998 he wrote a careful article for the Lancet, the British Medical Association journal, which showed the curious connection between vaccination injury and gastrointestinal disease.
Ten years after publication, Dr. Wakefield was targeted by the illness control system and his career was systematically destroyed. The medial establishment went so far as to withdraw his peer-reviewed, published paper claiming fraud on his part. He lost his license and fled to America, where he found friends to defend him.
I was with Dr. Wakefield at the Health Freedom Expo in Long Beach California at the beginning of March, 2012 and heard the news that the persecution is unraveling. It turns out that powerful media interests, with close “board room” links to Big Pharma, concocted the story of “fraud” in Dr. Wakefield’s original paper and it appears that the paid hack who broke the story of the alleged “fraud” himself falsified the records to persecute Dr. Wakefield. The Lancet cooperated in the persecution and now both the Murdock media interests and the Lancet are being sued for libel. The facts are clear: Dr. Wakefield’s name will be cleared and his reputation and license restored.
If the foreseeable harm that the toxic brew of which vaccines consist was not enough to warn everyone about the risks of vaccination; if the history of thousands of children maimed and killed was not enough to remind us of the first Rule of humane medicine — DO NO HARM! — the scientific evidence is now available that shows the “antibody immunity response” claimed for vaccines cannot be verified by science and the opposite is true: recent studies show “antibodies” have little, if anything, to do with immunity!
This just in from Ethan A. Huff, staff writer for Natural News –
“March 27, 2012 (NaturalNews) Bedrock of vaccination theory crumbles as science reveals antibodies not necessary to fight viruses
While the medical, pharmaceutical, and vaccine industries are busy pushing new vaccines for practically every condition under the sun, a new study published in the journal Immunity completely deconstructs the entire vaccination theory. It turns out that the body’s natural immune systems, comprised of both innate and adaptive components, work together to ward off disease without the need for antibody-producing vaccines.
The theory behind vaccines is that they mimic infection by spurring B cells, one of the two major types of white blood cells in the immune system, to produce antibodies as part of the adaptive immune system. It is widely believed that these vaccine-induced antibodies, which are part of the more specific adaptive immune system, teach the immune system how to directly respond to an infection before the body becomes exposed to it.
But the new research highlights the fact that innate immunity plays a significant role in fighting infections, and is perhaps more important than adaptive immunity at preventing or fighting infections. In tests, adaptive immune system antibodies were shown unable to fight infection by themselves, which in essence debunks the theory that vaccine-induced antibodies serve any legitimate function in preventing or fighting off infection.
“Our findings contradict the current view that antibodies are absolutely required to survive infection with viruses like VSV (vesicular stomatitis virus), and establish an unexpected function for B cells as custodians of macrophages in antiviral immunity,” said Dr. Uldrich H. von Andrian from Harvard Medical School. “It will be important to further dissect the role of antibodies and interferons in immunity against similar viruses that attack the nervous system, such as rabies, West Nile virus, and Encephalitis.” … as explained by Dr. Russell Blaylock in a recent interview with Mike Adams…”
What does this mean? it means the Myth is Busted!
There is no longer any scientific justification for further use of vaccines. Vaccination has been exposed as voodoo-science. From now on, there is no excuse for any physician who continues to push vaccines.
There is a better medicine than Big Biz Illness Control. There is a medicine that seeks Natural Solutions and that acts humanely, harmlessly. It is this medicine which is the future. The Illness Control system that has heretofore based its false promises on vaccination, on toxic drugs, on invasive techniques, is the pseudo-medicine of the crony coropratists and is now fully exposed for the lie it is.
I call upon all physicians, nurses, all health care practitioners, to take a stand today, against the deadly “medicine” pushed by the big lie of vaccination, I urge you to sign the Health Keepers Oath, swearing that your healing talents will never be used to harm the people who trust you with their health! Sign here: www.HealthKeepersOath.org.
For health & food freedom & justice, Dr. Rima www.HealMeDrRima.com
[Watch for live site; coming soon…]
PS – The medicine of the future is based on wholesome food, healthy lifestyles and potent nutritional supplementation. You can find very good sources of wholesome food and good nutrients at the beta site of our new International CSA, Consumer Supported Agriculture, www.FriendlyFoodCoOp.org.
Please Donate $9.99 Here and We will Send You the 2012 War Council Highlights
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The Initial Estimate of Situation Video “Revealed at the War Council: You are already being chipped…” – Dr. Rima http://youtu.be/3LHAwgq8Hwk
January 8, 2012 is Too Important to Miss!
Genomicide is Too Big to Succeed!
Stopping It is UP TO US!
Tiny URL for this page: http://tinyurl.com/2012WarCouncil ARCHIVE & Estimate of Situation (EoS)
ARCHIVE TO BE POSTED HERE
Link to General Bert’s written Estimate of Situation here: http://drrimatruthreports.com/?p=11666
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War Has Been Declared Against You, Your Family and Your Future. Genomicide is the Murder of Your Genetic Future. Join us for the 3rd Annual War Counsel as we say, “Stop Genomicide Now!”
Dr. Rima Raps – Making Genocide Audible
3rd Annual War Council
General Bert says, “Our Health, Our Food, Our Freedom and Justice are at stake. So are our lives. By the way, it is that important. Be there.”
Hildegard Stanninger, PhD: Global Brain Chip and Mesogens: Nano Machines for Ultimate Control of False Memories Foster Gamble: Making Sure “THRIVE” Is Not Just a Movie! Tim Bolen: Loosing a Generation: Thank you, CDC, the Center for Deadly Corruption Luba Diangar, MD: FDA Suppresses Radiation Free Mammography, Killing Women, Protecting Industry Sharry Edwards, MEd Making Truth Audible: Free BioAcoustics programs for Health & Food Freedom & Justice advocates…
Plus Dr. Rima, General Bert and Counsel Ralph.
As you decide how you are going to attend the 3rd Annual Natural Solutions Foundation War Council,I wanted to share his note I wrote to Dr. Stanninger, a featured speaker at the T3 Annual War Council, and a valued guest on our Internet radio program, heard live (and via archives) every Sunday from 10 AM to noon, Eastern, www.HealthFreedomPortal.org .
Dear Dr. Stanninger,
War has been declared against the people of Earth. But we are not ready to be the Every year for the past few years, Natural Solutions Foundation has brought people together at the beginning of the year for a War Council, to discuss where we have been and where we will be.
It was our pleasure to have you as one of our distinguished presenters at the First Annual War Council in 2010. I know that no one who heard you speak has forgotten your presentation!
This year, the 3rd Annual War Council will take place on January 8, 2012: People can attend live, via Webinar or Internet Radio. We would be honored to have you as one of our guests.
Our Mission is, in sum, “…to discover, develop, document, demonstrate and disseminate natural solutions to the impediment surrounding health and food coupled with achieving and maintaining a healthy self, community and world.”
But first, a bit of history: Gen. Bert (Maj. Gen. Albert N. Stubblebine III [US Army, Ret.]), our Foundation President and I had been growing increasingly distressed and concerned over the loss of our health freedom, briefly defined as our ability to exercise sovereign control over our own bodies through access to clean, unadulterated food, natural health options, the right to refuse coercive medial or other treatment and the free flow of information about health options.
We saw that the clearly articulated population reduction intentions of the globalists were being expressed through deadly and infertility-inducing drugs and vaccines (e.g., FDA, CDC, WHO, etc.), a degraded world food supply (e.g., USDA, Codex Alimentarius,WTO, WHO, FAO, ETC.), suppression of nutrients and related information (e.g., EFSD, FDA) and other genocidal tools deployed globally at an ever-accelerating pace.
We became so concerned, in fact, by the escalating developments and the fact that the people “on our side” appeared to be incapable of strategic analysis coupled with tactical deployment BEFORE the fact that we decided to close our highly successful medical practice (I was graduated from the Albert Einstein College of Medicine in 1970 and have practiced totally drug free medicine and psychiatry since then), create the Natural Solutions Foundation in late 2004 and, quite literally, marshal the forces and resources necessary to derail the genocidal globalist agenda.*
Codex Alimentarius, by the way, was created as an intentionally genocidal tool by the newly-released German genocidalist heads of IG Farben, the gigantic German civilian war machine. See my video, Nutricide, and my detailed article examining its development, The Killing Fields of Codex.
Since I had been watching the steady, and deadly, progress of Codex Alimentarius for more than a decade, and since the wildly destructive Codex Vitamin and Mineral Guideline was due for ratification on July 4, 2005, a mere half year away, one of the first things we did was approach Counsel Ralph Fucetola, JD, and ask him to solve the Codex Alimentarius problem at the legal level, creating a solution which any nation in the world, including the most nutritionally and economically fragile, could apply without engendering WTO trade sanctions.
He agreed and, with the able participation of Jim Turner, JD, these remarkable gentlemen put together the Codex Two Step Process. I turned it into a book, The Codex Book, which serves as a step by step guide and case study for the development of WTO Trade Sanction-Proof deviation from any of the Codex Standards and Guidelines for every nation which chooses this path for itself. You can download it Here.
The Foundation also produced a video of instruction on this tactic for Codex Delegates, which you can watch for free.
Once the book was complete and the legal strategy was perfected (and nations which have followed our Codex Two Step Process have, indeed, prevailed at the WTO dispute resolution level), Gen. Bert and I took to the road, visiting those countries which had not yet become the practical property of the Uber Cartel: Big Pharma and Big Medica which are Big Agribiz, which is Big Chema, which is Big BioTech, which is Big Pharma and Bigt Medica. We selected those countries which we felt still had a capacity to make their own food autonomy and sovereignty decisions.
We traveled widely in Africa and Asia meeting with heads of State, Ministers of Agriculture, Education and Health. When in India, for example, we had a private meeting with then-president Dr. A. P. J. Abdul Kalaam through the good offices of our dear friend, Dr. Monapa Hegde, MD in which we informed Dr. Kalaam about the problem, the WTO trade sanctions, etc. In fact, we were invited to help develop the regulations for the new Food Bill passed within a few weeks of our visit.
While traveling, I might add) in those countries which we felt could break away from the stranglehold of Codex and its industrially degraded food supply we realized that the Natural Solutions Foundation needed to create an Eco Demonstration Project which we could use as a school and training center for the BeyondOrganic BioDynamic Zero Emissions™ system of agriculture which can literally feed the world’s population without the use of chemicals, increasing crop yield, decreasing water use, increasing storage life, producing positive energy flow by generating more power than used from inexpensive, safe, intuitive, totally non-contaminating technologies and accomplish two things:
1. create a local inexpensive clean food supply at the highest standards and
2. create an international market for those clean foods at a premium market.
We have been gifted by a supportive universe, it would seem, with a number of technologies with which to do exactly that and they are available for deployment at minimal cost, requiring no education, no special machinery, no replacement, but requiring attention to restoration of the fertility and diversity of the microcosm of the soil. Fortunately, we have technologies for that as well to rapidly and safely clean the soil of petrochemical residues and restore high level fertility to it.
We understand, as I know you do, that the health of a populace is directly related to the life sustaining capability and capacities of its food supply, which includes its herbs and nutrients.
We anticipate that not only will the widespread application of this program increase the effective wealth of the society, starting with its farmers, enabling them to stay on the land and earn a decent wage (thus thwarting one of the major thrusts of the globalist genocidal agenda: the industrialization of food and food production) because of the decrease in the cost of seed and supplies, but the actual wealth of the society will be increased by the decline in health care costs and the sale of affordable food on the domestic market and premium food on the international market.
Additionally, through the support of market strategies which provide a ready, and fairly priced, market system for the farmers, and a connection to their customers, the social fabric of the local and larger communities will be strengthened.
And we believe, based on our investigation of the most promising food production regions of the planet, that one of the two most important potential food production areas in the world is the Indus-Ganges Basin, despite the considerable challenges which its sustainable, responsible, clean and socially responsible exploitation presents.
Fine theory, of course, but useless unless put into action. When we established our Valley of the Moon Eco Demonstration Project in Volcan, Chiriqui, Panama, we decided to incorporate clean food technologies and techniques, natural health technologies and techniques and social structure support (including farmer education, market strategies, land reclamation, etc.
Since premium Panamanian coffee is a critically important cash crop, heavily sprayed and contaminated to prevent crop loss (and resulting in horrific health problems for workers and consumers alike, to say nothing of the ecological devastation caused by conventional coffee growing techniques), we purchased an abandoned, derelict coffee “finca”or farm and reclaimed it according to our principles, sharing then freely with all interested parties.
Although we did not expect to have a decent crop for 3 years, our first year of harvest of Valley of the Moon™ Friendly Food Certified Coffee (Friendly to the Earth, to the Worker and to the Consumer) was outstanding. www.ValleyoftheMoonCoffee.com
Using more of same as our sole input, we have created a stunningly good coffee. We are now expanding our production to more derelict farms in the area (farmers here cannot afford the chemical sprays so increasing numbers are simply forced to abandon their fields, a situation not unlike many world-wide). Our coffee is seriously under-priced, according to the experts. Our crop has doubled each of the 4 years we have harvested and roasted our coffee.
The possibilities for other food production, animal and plant based, in Panama and around the world, is virtually limitless.
We envision a series of linked classrooms, market structures, health systems and educational inputs which are, literally, globe- and game-changing — and we look forward to discussing all this with you.
Meanwhile, perhaps you would find my new video, Making Genocide Audible, to be of interest.This video, like so much of our work at the Natural Solutions Foundation, is to help people face the unbearable squarely, with clear minded determination born of understanding, to have the information and strength to avert that unbearable reality.
Weaponized Pathogens —
— like the fake avian & swine flu “pandemics” or the new super-e. coli, plague DNA inserted; Weaponized “Phude” —
— fake food — dangerous GMOs & degraded organic standards; the “fruit” of Codex Alimentarius; Weaponized Vaccines (& Other Drugs) —
— with their childhood-destroying toxins, and Weaponized Environment;
— radioactive & toxic, in a vile synergistic mix.
All of this leading to Genocide via Genomicide…
I look forward, as do my fellow Trustees, Gen. Bert and Ralph Fucetola, JD, to your input, planning and of understanding depth to spread the reality, and halt the genocidal march…
For Health & Food Freedom & Justice, Dr. Rima
Rima E. Laibow, MD
Natural Solutions Foundation
Natural Solutions Foundation
Your Voice of Global Health & Food Freedom™
Dr. Rima reports: Sunday Mornings 10 to 1 EDT:
Special Announcement to Our Advanced Health Care Practitioners and All Friends of Food and Health Freedom
You know the importance of Compounding Pharmacies for your Practice. You know what the FDA is doing right now to that source of natural remedies.
We have an opportunity to acquire a state-of-the-art Compounding Pharmacy. If you are interested, contact our counsel, email@example.com.
Time is of the essence.
The FDA was the only Non Security US Govt Agency increasing budget… but this is, in fact, a military move: weaponized, industrialized food is a weapon of the war on us. It is part of the weaponized world – http://drrimatruthreports.com/?p=9617
We need to engage on OUR territory and the purchase of an off shore, fully triple-licensed compounding pharmacy brings the battle to our territory, our way, on our terms.
The Fund for Natural Solutions, www.FundforNaturalSolutions.org, is ready to purchase a fully licensed, clean-room equipped Compounding Pharmacy in which we can
1. Make, sell and export the now-banned bio-identical hormones which the FDA has attacked in the US
2. Make, sell and export the now-banned and increasingly criminalized nutrients, supplements and herbals which the FDA and European Food Supplements Directives have attacked in the US and Europe
3. Make, sell and export intravenous, transdermal, oral and suppository nutrients and wellness compounds which the FDA and European Union are increasingly attacking and banning in the US and Europe
What does it take to protect wellness, and YOUR access to wellness products? We need your investment in the newly renamed Fund for Natural Solutions. And time is short.
A pharmaceutical company is about to close the deal on the only certified clean room, GMP Compounding Pharmacy we know of which available to us, the Wellness Team.
We have every reason to believe that the Compounding Pharmacy will be a significant profit center and every reason to believe that the government in which this company is located will never again license another such Compounding Pharmacy: they told us so!
Investing in the Compounding Pharmacy Project of the Fund for Natural Solutions makes sense: our side needs the money to carry out profitable, important projects like this.
Ready to help?
Ready to get involved?
Ready to put your money exactly where your beliefs are and get it offshore at the same time?
IRAs, 401 funds, conventional funds, trust and church funds, etc., make it possible for our side to take effective, and we believe, profitable, steps.
The minimum investment for the Fund for Natural Solutions is $10,000. The minimum investment for the Compounding Pharmacy Project is $100,000. We have a few days to secure this company.
Support the Natural Solutions Foundation’s “Stop the Shot” Federal Lawsuit to prevent the use of any influenza vaccine. Set up a recurring donation now:http://drrimatruthreports.com/?page_id=189
This long, detailed and immensely important article makes it crystal clear where the lies and distortions are about vaccines, whether they work, whether they cause chronic illnesses and whether they are safe.
Before you allow yourself or your wards, children, family, elders or others to take another vaccination, read this article. Listen to Dr. King discuss this article on the Dr. Rima Reports live (www.HealthFreedomPortal.org to join the chat and listen to the show or at www.OracleBroadcasting.com to listen to the show or in the archives at www.OracleBroadcasting.com following the broadcast on Sunday, October 3, 2010, 10 AM to 1 PM Eastern time.
Dr. King knows full well that vaccines are intentionally used to create disease and profit while they do nothing to prevent disease. Listen to him, read the article below and share this article as widely as possible.
Thanks for your activism. Yours in health and freedom,
Vaccines, Vaccination Programs and Knowing1 Misrepresentations
Paul G. King, PhD
Facility Automation Management Engineering (FAME) Systems
33A Hoffman Avenue, Lake Hiawatha, NJ 07034-1922
Before discussing the subjects in the title of this article, this commenter would be remiss if
he did not first set forth his biases and conflicts concerning the issues discussed in the sections and
paragraphs that follow this introduction.
As a scientist who understands that:
? Terms must be clearly defined,
? Statements must be supported by factual evidence and, where that evidence is not
readily available, appropriate citations thereto,
? Much of the information on vaccines and vaccination programs available in the
mainstream media and publications backed by the Establishment and its minions is
more propaganda, cant and Orwellian newspeak than sound science, and
? Vaccines or vaccination programs where the vaccine is reasonably safe and the
protection provided is either life saving (e.g., the rabies vaccines) or the prophylactic
vaccine is reasonably safe and effective in protecting almost all (i.e., >90 %) of those
vaccinated, long-lasting (i.e., protects that not less than 90 % of those vaccinated for
a period of not less than 50 years), and medically cost-effective, for example, the
measles only vaccine and vaccination program) should be supported,
this commenter must stand against: a) the misrepresentation of vaccines and vaccination programs
in any manner, and b) vaccination programs in which: i) those inoculated with the vaccine are not
protected or ii) more who are vaccinated suffer serious adverse injury from the vaccine than there
are disease cases in the population segments that are being vaccinated (e.g., the early childhood
hepatitis B vaccination program).
In addition, since the Establishment continually spews out a never-ending stream of near-
religious vaccine and vaccination apologia, this author sees no need to spend any time discussing
the inflated and often deceptive presentation of vaccines and vaccination programs as the
“salvation” of mankind – because such discussions belong in the realm of religion and not science.
With the preceding in mind, this author will now begin to address fundamental vaccine and
vaccination-program misrepresentations that stand in the way of our right to choose or decline any
prophylactic medical treatment, including any prophylactic inoculation with any vaccine or serum
as we, and not society, sees fit for ourselves and the minors and non-competent persons in our care.
1. “Vaccines Are Safe”
The first misrepresentation about vaccines and by far the worst is that, as a group (or
individually), “vaccines are the safest of medicines” or, more simplistically, “vaccines are safe”.
The factual evidence and the legislation protecting the vaccine makers, vaccine providers
Where the term “knowing” is used in the “knowingly” or “knew” sense that is defined in 21 U.S.C. § 321(bb) “The
term “knowingly” or “knew” means that a person, with respect to information – (1) has actual knowledge of the
information, or (2) acts in deliberate ignorance or reckless disregard of the truth or falsity of the information”.
and the healthcare establishment clearly exposes a different reality, which, in its most telling form,
can be found in the National Vaccine Injury Compensation Program (NVICP2; Title 42 of the
United States Code in Sections 300aa-10 through 300aa-34 [42 U.S.C. § 300aa-10 – 300aa-34]) in §
300aa-22(b)(1) which, under: a) the umbrella of “Standards of Responsibility” (§ 300aa-22.) and b)
the heading at § 300aa-22(b), “Unavoidable adverse side effects; warnings”, states:
“No vaccine manufacturer shall be liable in a civil action for damages arising from a
vaccine-related injury or death associated with the administration of a vaccine after
October 1, 1988, if the injury or death resulted from side effects that were unavoidable even
though the vaccine was properly prepared and was accompanied by proper directions and
warnings”. [Emphasis added]
If vaccines were truly safe, then there would be no need for: a) any NVICP legislation to
protect the vaccine makers or the healthcare providers from civil lawsuits for damages, or b) any “if
the injury or death resulted from side effects that were unavoidable” language to absolve vaccine
manufacturers from damages that include “vaccine-related injury or death”.
Clearly, unbiased scientists, the federal lawmakers, and the informed public know that, as a
group or, in most instances, individually, vaccines are not the safest medicines.
2. “Vaccines Are Effective”
If vaccines were truly effective, then there would be:
a. No need for any State to mandate any vaccination program for any vaccine –
everyone would be demanding inoculations for themselves and their loved ones,
b. No need for any mention of the unproven theory of “herd immunity”, which, in
reality, can only be a theory of “herd protection” because vaccines do not provide
blanket immunity (defined as lifetime [>50 year] protection from disease) to even
those who have been inoculated with the recommended vaccines from 2 to 6 or more
times, depending upon the vaccine, and
c. No need to license vaccines based on their manufacturers’ claimed levels of
“efficacy” as measured by some minimum-antibody-level surrogate for
Given the preceding factual realities, it is clear to any rational person that unqualified
phrases, like “vaccines are safe” and “vaccination programs are effective”, are simply propaganda
slogans that vaccine makers, the healthcare establishment, pro-vaccine academics, pro-vaccine US
governmental agencies (e.g., Department of Health and Human Services [DHHS], the Centers for
Disease Control and Prevention [CDC], the Food and Drug Administration [FDA], the National
Institutes of Health [NIH] and the Public Health Service [PHS], to name a few) and other vaccine
apologists continually use in their efforts to both brainwash and coerce the public into accepting
whatever vaccines and vaccination programs that “these groups” have decided, at a given point in
time, are “good” for the public as a whole with little or no regard for the fiscal or physical health of
The full title of the NVICP in the United States Code is: TITLE 42 – THE PUBLIC HEALTH AND
WELFARE, CHAPTER 6A – PUBLIC HEALTH SERVICE, SUBCHAPTER XIX – VACCINES, Part 2 –
National Vaccine Injury Compensation Program.
any individual or individuals that such vaccination programs may harm, maim or kill or, for that
matter, the fiscal and physical health of the people of the United States Of America (USA).
3. “Vaccine Panacea: The More Vaccines We Get, The Healthier We Will Be”
a. The Legacy (Pre-NVICP) Vaccination Programs
Reviewing the history of vaccines and vaccination programs in the USA, up until the early
1900s, the only widely used human prophylactic (disease-preventive) vaccine was the live-virus
cowpox vaccine, vaccina; the only other general human-use vaccine was the attenuated rabies
vaccine used to treat people who had been bitten by a rabid animal; and the only large-scale mass
“vaccination” program was the “smallpox” inoculation program.
In the 1920s, a diphtheria vaccine was introduced and its use spread; in the 1950s, the use of
pertussis vaccines became widespread but these morphed into the first combination the DTP
vaccine, which was to become the first Thimerosal-preserved combination vaccine to be used in a
mass vaccination program.
In the 1950s, the Salk inactivated-polio vaccines were introduced for mass use without
adequate testing and purity leading to: a) an initial increase in paralytic polio cases until the clinical
definition of paralytic polio was changed and b) the introduction of SV-40 and other animal viruses
which were, to varying degrees and levels, contaminants of all the polio vaccines produced for the
next three decades; and, a few years later in the early 1960s, the live-virus Sabin oral polio vaccines
displaced the Salk inactivated-polio vaccines – the Sabin oral polio vaccines were used in the USA
until 2000 when, because all paralytic polio cases were cases caused by exposure to the vaccine-
strains of the live vaccine, the US switched back to a Salk-type inactivated-virus polio vaccines,
which is still in use today.
In 1963, a live-virus measles vaccine was introduced and put into mass use shortly after its
introduction; the measles-only vaccine was followed by a measles-rubella (Merck’s measles-rubella
vaccines, MR® and MR® II, that have been discontinued); then a measles-mumps-rubella vaccine
(Merck’s MMR® vaccine); and finally an improved measles-mumps-rubella vaccine (Merck’s
MMR® II vaccine)3.
In the early 1980s, though some other vaccines were being licensed, they were not being
recommended for mass use in childhood vaccination programs because of the increasing number of
lawsuits where the parents of vaccine-injured children, principally by the DTP vaccines and the
Polio vaccines but also by the measles and MMR vaccines, were winning ever larger monetary
judgments against the vaccine companies.
Faced with decreasing profit from the lawsuits, the major vaccine makers threatened to stop
making vaccines unless the government passed legislation that protected them from most all direct
civil legal actions for the harm their vaccines caused in some of the children who were being
inoculated with these vaccines.
In addition to the combination measles-mumps-rubella vaccines (MMR® and then MMR® II), Merck continued to
make the individual component vaccines, Attenuvax®, Mumpsvac®, and Meruvax® II until the mid-2000s. In 2010,
Merck announced that, in spite of customer demand for the individual vaccines, Merck would not resume
producing these vaccines.
from the pen of Paul G. King, PhD
In late 1986, comprehensive legislation was enacted that included the National Vaccine
Injury Compensation Program (NVICP) that was codified in 42 U.S.C. §§ 300aa-10 through 300aa-
34 and, in stages, became effective in 1987 and 1988.
This legislation was originally supposed to: a) provide a speedy, “no fault”, non-litigious,
fair compensation program for vaccine-injured children and their families, which, after initial
appropriations to start the program, was to be paid for by a tax on each disease component in each
dose of vaccine administered, and b) shield the vaccine makers from being easily sued.
In return for this protection, the vaccine manufacturers were supposed to make ever-safer
vaccines that caused less adverse reactions under strict governmental oversight that would not only
compel vaccine makers to make safer vaccines but punish them when they did not make vaccines as
safe as possible and reduce the risk of adverse reactions.
In actuality, all that the NVICP has done is shield the vaccine makers from being sued and,
through an increasingly slow, litigious, convoluted, and unfairly administered “compensation
program”, its administrative hearings have only compensated a very small percentage of those who
are damaged by adverse reactions to vaccines even though the program has been expanded to
include adults in many instances.
In 1987, Congress took the first action to decrease the fairness of the program and reduce the
financial burden on the federal government and the vaccine makers for any violation by repealing §
300aa-18, which indexed the compensation for both vaccine-related death and the vaccine
manufacturers’ fines to the rate of inflation.
Next, the NVICP program administrators started making it harder for children’s families to
collect for vaccine injuries by, in the 1990s, removing many of the indications from the “Vaccine
Injury Table” (see: Sec. 300aa-14. Vaccine Injury Table) without any independent scientifically
sound justification for removing them, which forced many more cases to be heard in a proceeding
that has become increasingly litigious and unfair4.
In the late 1980s, though it was clear that the diphtheria, tetanus, acellular pertussis (DTaP)
vaccines produced a lower rate of adverse reactions in children given them than the corresponding
diphtheria, tetanus, whole-cell pertussis (DTwP) vaccine, based on the data from Japan, which
introduced the DTaP vaccine in 1981 and saw a sharp decline in both diphtheria-tetanus-pertussis-
vaccine-related adverse reactions and vaccine-related deaths, the DTwP vaccines were still licensed
and being given in the USA until 1997, when the vaccine makers finally switched to making the
This continual indication reduction process has gone beyond the absurd, removing the rotavirus vaccine indication
for intussusception even though all of the rotaviruses have been shown to cause intussusception in some vaccinated
children and two new rotaviruses (a 5-component bovine-human hybrid rotavirus vaccine [RotaTeq®] and an
attenuated human rotavirus vaccine [Rotarix®]) have been licensed and approved for mass use instead of amending
the table entry for the withdrawn RotaShield ® rhesus-monkey/human hybrid rotavirus vaccine and, most recently,
proposing to further alter the allowable time windows for the few remaining indications in the Vaccine Injury Table
(see: Federal Register / Vol. 75, No. 176 / Monday, September 13, 2010 / Proposed Rules / 55503 – 55507).
As one article correctly reports, “4) The old whole-cell version of DPT, given until about 1997 in the US, was bad. It
had a high rate of serious reactions, and these researchers calculated its effectiveness at only around 48%. But for the
previous 20 years, parents in the US were being told their children must have this vaccine. The real truth about a
After all, after 1986, the vaccine maker’s principal goad to make safer vaccines, the
monetary awards to successful plaintiffs in civil court cases seeking compensation for the injuries
caused by their vaccines, had been removed.
By comparison, the legal replacement for this goad was a weak and obviously ineffectual
federal governmental bureaucracy over which the vaccine makers obviously had significant
influence, and, given Merck’s Gardasil HPV vaccines’ problems and the federal government’s
failure to take any substantial action against the vaccine or the vaccine maker, currently have even
b. The NVICP and Post-NVICP Vaccination Programs
With the passage of the NVICP legislation, the stream of vaccines from a growing number
of vaccine makers and/or their subsidiaries has increased to a veritable river.
Discarding any semblance of a need for cost-effectiveness in any mass vaccination program,
the Establishment has moved to not only add more doses of vaccines that were already marginally
cost-effective or not even cost effective but also to propagandize vaccination programs where the
underlying vaccine is not even truly effective or, in some cases, not even reasonably safe.
In addition, the Establishment, using a hired Institute of Medicine (IOM) committee as its
surrogate, redefined the allowable “placebo” in a vaccine clinical safety trial from only a pH-
buffered sterile isotonic saline solution to include: a) the entire vaccine formulation without the
active antigens, b) some other experimental vaccine or c) some other licensed vaccine, and
convinced the regulators to look at relative incidence of adverse events instead of their absolute
incidence in determining that a given vaccine is “reasonably safe”.
Together, these changes altered the basis for “safety” in phase 3 clinical trials and, by
increasing the adverse reactions in the “placebo” group, reduced the relative level of each adverse
reaction in the candidate vaccine compared to that adverse reaction in the “placebo” group.
Thus, when “three” children in the test group for Merck’s RotaTeq® vaccine in as clinical
trial (conducted in an overall population where sanitation is poor) developed intussusception and
“one” child in the control group developed intussusception, the RotaTeq vaccine was still
approvable and approved because the rate of intussusception was not significantly higher (on a
statistical basis) than the rate in the controls because of the small size of the groups in phase 3 trial
that Merck had conducted.
On this basis, the FDA licensed Merck’s genetically engineered, bovine-human-hybridized,
pentavalent, oral, live-virus rotavirus vaccine, RotaTeq, even though this vaccine’s actual rate of
intussusception was 3 times that found in the control group.
Of course, after its approval in February of 2006, the pediatricians were told that, unlike the
previous “intussusception prone” rotavirus vaccine, Wyeth’s RotaShield®, which was withdrawn
shortly after its introduction in 1998, RotaTeq’s on-label use would not cause intussusception.
Even after being told that RotaTeq does not cause intussusception, the RotaTeq-related
intussusception signal in the voluntary Vaccine Adverse-Event Reporting System (VAERS) [where
particular vaccine being kind of dangerous and ineffective doesn’t come out until the pharmaceuticals decide they
have something better” (emphasis added). [See: http://www.exploringvaccines.com/?p=686]
typically less than 10% of actual adverse events for a given vaccine are reported] was even larger
after RotaTeq began to be used than the signal seen from the previous, now-withdrawn
“intussusception prone” RotaShield rotavirus vaccine and, in addition, RotaTeq-related cases of
Kawasaki’s disease were also reported6.
Additionally, after the NVICP was enacted, several patently unsafe or problematic vaccines
were licensed (e.g., LymeRX™ for Lyme disease and RotaShield® for rotavirus) and, after causing
horrendous or significant harm to those vaccinated with them from which the Establishment
profited, simply withdrawn from the market.
Thus, in addition to the pre-NVICP childhood vaccination programs for DTP, MMR and
Polio, we now have ineffective and/or less-than-effective vaccines and less-than-effective and/or
non-cost-effective mass vaccination programs for: a) late-childhood/adult diphtheria-pertussis-
tetanus (Tdap), b) childhood Haemophilus influenzae, type B (Hib), c) early childhood/adult
Hepatitis B (Hep B), d) childhood chickenpox, e) childhood/adult Hepatitis A (Hep A), f)
childhood/adult meningococcal meningitis (Sanofi Pasteur’s Menomune® and Menactra® vaccines),
g) Streptococcus pneumoniae (Wyeth’s Prevnar® and Prevnar ® 13[childhood] and Merck’s 23-
valent Pneumovax® [adult]), h) childhood rotavirus (Merck’s RotaTeq® and GlaxoSmithKline’s
(GSK’s Rotarix®), i) adult Shingles, and j) mid-childhood/young-adult human papilloma virus
(HPV; Merck’s Gardasil® and GSK’s Cevarix®) as well as k) ineffective annual vaccines and
annual vaccination programs for viral influenza in children and adults with “11” different vaccine
formulations currently being produced in “eight” manufacturing sites.
Moreover, not only does this require more and more vaccines to be given during childhood
but also, further unmasking the reality that vaccination is not immunization, to increase “coverage”
(in reality, market size and market penetration), adults are increasingly recommended to: a) get
“boosters” doses or “booster” vaccines, b) get periodic Tdap boosters in lieu of tetanus boosters,
and c) accept additional vaccine doses whenever there is a disease outbreak of a “vaccine
preventable” disease in their community regardless of their disease status.
In addition, no meaningful action has been taken against the vaccine makers for their failure
to expeditiously safen US vaccines by removing all preservatives and reducing the level of
adjuvants used or, where possible, eliminating the use of adjuvants altogether.
Instead, though there currently is a limit on the permitted level of aluminum adjuvant in
each vaccine7, the total level of aluminum adjuvants administered is being allowed to increase
without limit and the vaccine makers are increasingly demanding that they be permitted to use so-
called “oil-in-water” adjuvant systems even though, based on animal usage, these are known to be
more serious immune-system disruptors than the current long-used aluminum adjuvants whose
long-term safety for use in human vaccines has not been proven individually much less collectively.
Geier DA, King PG, Sykes LK, Geier MR RotaTeq vaccine adverse events and policy considerations. Med Sci
Monit. 2008 Mar; 14(3): PH9-PH16.
If the FDA’s proposed changes to 21 CFR § 610.15. Requirements for constituent material as published in the
Federal Register (see: Federal Register 2010 March 30; 75(60): 15639-15642) are adopted by the FDA, the FDA
will be able to waive all of the current limits, including those for preservatives and adjuvants as it sees fit even
though doing so is a subversion of the foundation upon which the regulation o all drugs is based – the applicable
regulations as set forth in 21 CFR Parts 600-680 are current good manufacturing practice (CGMP) minimums,
which every covered biological drug product must meet.
Finally, in spite of being sued for the failure of the Secretary of the Department of Health
and Human Services (hereinafter, the Secretary) to make vaccines safer and reduce the risk of
adverse reactions, as required by 42 U.S.C. § 300aa-27(a), by removing Thimerosal (49.55 %
mercury by weight) from the list of approved chemicals that can be used to manufacture vaccine,
the federal government has yet to ban the use of Thimerosal, a chemical that is known to induce
anaphylactic shock in some and mercury poison susceptible developing children, in the manufacture
c. The Number of Vaccine ‘Doses’ Reality
Increasingly the public is being told that they must submit to ever-expanding vaccination
programs for themselves and their children without regard for the risks to their own health or the
health of their children because complying is for the “greater good”.
For children up to 6 years of age, the recommended vaccination program reached a new high
in 2009 when, in addition to all of the 38 vaccines in the 2007 and 2008 vaccination programs, three
more doses of an 2009-A-H1N1 influenza vaccine was added for a nominal total of 41 doses of
Relative to 1983, the maximum relative level of mercury from possibly Thimerosal-
preserved vaccines (marked in red in Table 1 on the next page) was 1.6 times the nominal level of
exposure in 1983 and, roughly correcting for 10-or-more-times-larger effect of the prenatal
mercury dose, effectively up to 5-plus times the level of adverse impact relative to the vaccine
exposure to injected Thimerosal (49.55% mercury by weight) in 1983.
d. The Continuing Use of Mercury (Thimerosal, 49.55% Mercury by Weight) Reality
When it comes to the issues surrounding the serious adverse health impacts of Thimerosal
(49.55% mercury by weight) on those vaccinated with vaccines containing it, the public is
continually propagandized with one of two misleading and inaccurate slogans:
1. “Mercury has been removed from all childhood vaccines” or
2. “All vaccines given to children, except some flu vaccines, no longer contain any added
The reality is that the Establishment, faced with a growing public outcry against the use of
Thimerosal as a preservative in childhood vaccines, did gradually reduce the level of Thimerosal in
the previously Thimerosal-preserved vaccines from nominally 25 micrograms of mercury per 0.5-
mL dose to about 1 mcg of mercury per 0.5-mL dose (a reduced-Thimerosal or “trace”-Thimerosal
vaccine formulation) in the period from 2001 to 2005 and then starting in 2004, phased out the use
of Thimerosal in childhood vaccines.
However, to offset this reduction in mercury exposure from childhood vaccines (and the
serum Rho(D) products), the Establishment-controlled CDC began publishing recommendations in
April of 2002 that, during the annual flu season: a) pregnant women who would be in their second
and third trimesters and b) children 6 months to 23 months of age should get a flu shot (see
Prevention and Control of Influenza Recommendations of the Advisory Committee on
Immunization Practices [ACIP]. MMWR 2002 April 12; 51(RR03): 1-31) at a time when all FDA-
approved influenza vaccines were Thimerosal-preserved vaccines.
Table 1: The CDC-Recommended Vaccine Schedule Comparison in Children
from Conception to 6 Years of Age, By Year (Recommended Month)
Year USA 1983 USA 2007 USA 2009
Before Birth — Influenza shot
Seasonal influenza &
Birth through 1 Year DTP (2) Hep B (birth) Hep B (birth)
OPV (2) Hep B (1) Hep B (1)
DTP (4) DTaP (2) DTaP (2)
OPV (4) Hib (2) Hib (2)
DTP (6) IPV (2) IPV (2)
[5 total] PCV (2) PCV (2)
[75 mcg Hg] Rotavirus (2) Rotavirus (2)
Hep B (4) Hep B (4)
DTaP (4) DTaP (4)
Hib (4) Hib (4)
IPV (4) IPV (4)
PCV (4) PCV (4)
Rotavirus (4) Rotavirus (4)
Hep B (6) Hep B (6)
DTaP (6) DTaP (6)
Hib (6) Hib (6)
IPV (6) IPV (6)
PCV (6) PCV (6)
Influenza (6) Seasonal Influenza (6)
Rotavirus (6) 2009-A-H1N1 (6)
Influenza (7) Rotavirus (6)
 Seasonal Influenza (7)
[25; 50 mcg Hg] 2009-A-H1N1 (7)
[50; 100 mcg Hg]
1 through 2 years MMR (15) Hib (12) Hib (12)
DTP (18) MMR (12) MMR (12)
OPV (18) Varicella (12) Varicella (12)
[3; 8] PCV (12) PCV (12)
[25; 100 mcg Hg] Hep A (12) Hep A (12)
DTaP (15) DTaP (15)
Hep A (18) Hep A (18)
Influenza (18) Influenza (18)
[8; 30] [8; 33]
[12.5; 62.5 Hg] [12.5; 112.5 Hg]
2 through 3 years Influenza (30 Influenza (30
Influenza (42) Influenza (42)
[2; 32] [2; 35]
[37.5; 100 mcg Hg] [37.5; 150 mcg Hg]
4 through 6 years DTP (48) MMR (48) MMR (48)
OPV (48) DTaP (48) DTaP (48)
[2; 10] IPV (48) IPV (48)
Varicella (48-60) Varicella (48-60)
[25; 125 mcg Hg] Influenza (54) Influenza (54)
Influenza (66) Influenza (66)
[6; 38] [6; 41]
[50; 150 mcg Hg] [50; 200 mcg Hg]
Vaccines and values in a red font are for vaccines that were, in 1983, or, in the 2000s, may still
The CDC made these recommendations in spite of the fact that the flu vaccines were
“Pregnancy Category C” vaccines with no proof:
a. Of non-teratogenicity for the fetus or reproductive safety for the pregnant women;
b. That the flu vaccines were not mutagenic or carcinogenic; or
c. That the flu vaccines were in-use effective in preventing those vaccinated from
There was, as is the case today, also no proof that flu vaccines, of any kind, are more in-use
effective than a placebo injection in preventing those children under 2 years of age who are
inoculated with a flu vaccine from contracting influenza.
As: 1) the level in the childhood vaccines continued to declined, 2) some doses of “trace”-
Thimerosal flu vaccines became available, and c) a live-virus flu vaccine was introduced, the CDC
recommendations continued to try to maintain the adverse effects of the average level of mercury
exposure to Thimerosal by: a) removing the restriction as to when, during pregnancy in the flu
season, flu shots could be given; b) increasing the upper limit on children to first 35 months, then to
59 months, then to 107 months, and, finally, to 18 years of age; and c) requiring children to get two
flu shots (a month apart) the first time they were vaccinated.
In 2009, the maximum level of Thimerosal exposure was doubled in utero and at 6 months
and 7 months when the CDC: a) added the “pandemic”, “swine flu”, 2009-A-H1N1 influenza to the
vaccines recommended to be given once to pregnant women and twice to children under 9 years of
age, and b) also designated pregnant women and young children as targeted “high risk” groups.
? Most of the doses of available influenza vaccines are Thimerosal-preserved doses,
? The CDC steadfastly refuses to even express a preference for pregnant women and
young children to get “no Thimerosal” influenza vaccine doses and
? The FDA continues to illegally license Thimerosal-preserved vaccines for which the
vaccine manufacturer has never proven that the level of Thimerosal used as a
preservative in said inactivated-influenza vaccines is “sufficiently nontoxic …” as
required by the applicable portion of the current good manufacturing practice
(CGMP) safety regulations set forth in 21 CFR § 610.15(a),
pregnant women and children are continuing to be injected with toxic levels of mercury from
these adulterated drugs8
Moreover, given the CDC’s decision to increase the upper age limit for children to 18 years
and recommend that all adults be vaccinated annually, if Thimerosal-preserved flu shots continue to
be administered and some children and their mothers during pregnancy only get Thimerosal-
preserved flu shots, clearly the total dose of mercury exposure will continue to exceed the
maximum level that children born in the 1990s would have received from the three Thimerosal-
preserved childhood vaccines, DTaP, Hib, and Hep B, given to all children before 2001 and to some
Thimerosal-preserved vaccines for which the manufacturer has failed to meet the applicable clear CGMP minimum
“sufficiently nontoxic …” requirement for the vaccine dose set forth in 21 CFR § 610.15(a) are adulterated drugs
under 21 U.S.C. § 351(a)(2)(B).
from the pen of Paul G. King, PhD
children into the 2004 – 2005 timeframe, if no changes had been made to the Thimerosal-preserved
childhood vaccines or in the recommendations for the use of Thimerosal-preserved inactivated-
influenza vaccine formulations to inoculate pregnant women and developing children.
As long as the preceding realities continue to exist, any claim that there can be no link
between: a) the level of mercury exposure and b) the risk of neurodevelopmental disorders, chronic
illnesses and abnormal behaviors is obviously a specious claim because the maximum level of
mercury has not dropped from the 2000 level but rather the maximum exposure level has increased.
At the same time, the levels of neurodevelopmental disorders, chronic medical conditions,
and abnormal behaviors have not dropped but rather these levels have also collectively increased.
Based on the preceding and other key facts (e.g., the several-fold excess level of males as
compared to females in the neurodevelopmental disorders and the fact that increases in these
disorders were noticed a couple of years after the 3-dose regimens for Thimerosal-preserved Hep B
and for Hib were implemented in the late 1980s in the USA and in the 2000s after similar program
changes were implemented in New Delhi, India9), this author knows that mercury exposure from
Thimerosal in vaccines and other drugs is the major causative factor in many, if not all, of the
epidemic-level increases in neurodevelopmental disorders, chronic medical conditions, and
4. “The Benefits Outweigh The Risks”
Pointing to our current increased life expectancies and ignoring their projected future
decline, the Establishment continually tells Americans that the benefits of each new vaccination
program outweigh the risks.
Unfortunately, there has been epidemic increases in many chronic diseases (e.g., asthma in
children from < 1 in 1,000 children in the 1970s to > 1 in 10 children in the 2000s) and the
morphing of previous chronic diseases only seen in adults (e.g., type 2 diabetes) into chronic
diseases seen in children to the point that, in 2006, more than 26 % of American children have one
or more chronic diseases (up from 12.8 % in 1994)10 that they most probably will have over their
Thus, the “greater good” for whom each of us is supposed to sacrifice ourselves and our
loved ones is, in actuality, the “greater good” for one or more segments of an Establishment that
feeds on us and grows ever stronger as more of us weaken and become chronically ill and/or
financially and physically drained trying to care for our chronically ill loved ones.
Worse, there is increasing evidence that those who are effectively in control of this
Establishment decided have, unconsciously or consciously, that they need to:
The reality of this linkage was recently strongly reinforced by the emergence of a similar pattern’s being observed
in a New Delhi, India nursery school after the New Delhi pediatricians began recommending the addition of 3-
doses each Thimerosal-preserved Hib and Hep B vaccination programs to the Indian government’s recommended
Thimerosal-preserved DTP vaccination program in 2000 and the worsening of the outcomes when these programs,
originally designed to finish the 9-shot vaccination series by the time the children are 6 months of age, were
shortened to be completed by 4.5 months of age and the incidence of neurodevelopmental dysfunction doubled.
Van Cleave J, Gortmaker SL, Perrin JM. Dynamics of Obesity and Chronic Health Conditions Among Children
and Youth. JAMA 2010 February 17; 303(7): 623-630.
? Increase the harm,
? Further drain our fiscal and physical strength, and
? Reduce our numbers and our life expectancy, while feeding on our fiscal and physical
To that end, increasingly expensive vaccines (e.g., Merck’s Gardasil and GSK’s Cervarix,
where the private-sector list price for each dose is than US $125.0011) that: a) are less-and-less
curative and/or effective and b) seem to be more-and-more harmful are being approved and
delivered to the public as preventives for conditions whose incidence, in many instances, may have
been caused or aggravated by other vaccines, drugs, processed and genetically altered foods, and
chemicals that the Establishment markets to the public as “safe” without any real proofs of the
short-term and, more importantly, true long-term safety for any of these Establishment products.
To sell these less-than-effective, less-than-proven-safe, and much-more-expensive vaccines,
the Establishment continually reminds the public of the horrors of the deaths from “vaccine-
preventable disease” for certain highly contagious and lethal diseases from the era before vaccines
(e.g., smallpox, polio and measles), diseases that have disappeared (e.g., smallpox) or only occur at
low levels (e.g., measles) in the USA today, while ignoring or minimizing the following critical
? Clean water, sanitation, basic food safety, improved housing, and antibiotics did
more to reduce the level of the disease-related injuries and fatalities from the highly
contagious and lethal diseases than the vaccines for them have done,
? Without any vaccine, scarlet fever, a highly contagious and lethal disease, has
? Many of today’s vaccines are for diseases that: a) are not highly contagious (e.g.,
influenza and hepatitis B) or b) do not have any significant mortality levels (e.g.,
chickenpox, mumps, rubella, and tetanus).
? The obviously vaccine-related increases in chronic diseases, especially chronic
diseases that have a significant autoimmune component, like asthma, multiple
sclerosis, chronic fatigue syndrome, lupus, and diabetes, to name a few, as well as
epidemic increases in abnormal childhood neurodevelopment, abnormal behaviors,
other developmental abnormalities and bowel disorders.
In addition, when we were first being sold on mass vaccination programs as a means to
protect the health of the public, we were told that a mass vaccination program for any vaccine
depended on the vaccine’s being effective and the mass vaccination program’s being cost effective.
Consider the “chickenpox” vaccination program where the vaccine, Merck’s Varivax®, is a
live-virus vaccine that infects every one inoculated with it with a certain strain, the Oka/Merck
strain, of herpes varicella zoster (HVZ) – a vaccine strain that is not effective in preventing
CDC Vaccine Price List (Prices last reviewed/updated: September 24, 2010): Merck’s HPV-Quadrivalent (Types 6,
11, 16 and 18) Recombinant Vaccine, Gardasil, US$ 130.27/dose; GSK’s HPV-Bivalent (Types 16 and 18)
Recombinant Vaccine, Cervarix, $ 128.75/dose, where both process include a US$ 0.75 excise tax nominally
collected for the NVICP in 10-dose vials: $1302.70 plus shipping and handling for each Gardasil vial and $1287.50
vial. The commercial list price costs of the two 3-dose series are US$ 390.81 and US$ 386.25, respectively.
from the pen of Paul G. King, PhD
everyone vaccinated, or even all of those with a “sufficient” vaccine-strain antibody titer level, from
also being infected by the “native”/“wild” strains of HVZ circulating in the USA.
When the initial licensing for this vaccine was sought in the 1990s, the justification for
licensing a chickenpox vaccine for a normally mild and innocuous childhood disease was that
vaccination was marginally cost-effectiveness on a societal productivity-loss basis under the
presumptions that: a) one dose of vaccine would provide lifetime protection for most young
children inoculated with the vaccine and b) there would be no serious adverse reactions to being
inoculated with the vaccine.
Yet, today, two doses of Varivax® are the minimum recommended for all children, and older
adults are being recommended to receive a dose of Merck’s Zostavax®, a higher-concentration Oka-
strain HVZ vaccine to “prevent” a recurrence of the HVZ (native or vaccine-strain) with which they
have been infected.
Without even considering the costs to treat those who have severe adverse reactions to the
Varivax or Zostavax vaccines, a conservative 2009 cost analysis placed the US excess shingles’
cases’ costs, caused by the US childhood chickenpox vaccination program, at US$ 700 million
Clearly, the Establishment has discarded the requirements for vaccine effectiveness and
In their place, Establishment profitability seems to have: a) overruled the federal
government’s concern for public’s fiscal and physical health and b) trumped the significant costs
from the collective long-term vaccination-induced physical harm, including maiming and death,
that some of those who are vaccinated suffer12 when the serious adverse effects caused by the initial
vaccine, Varivax® (which was claimed to cause no serious adverse effects in the FDA-
licensing/approval process), Merck’s MMR-Varicella vaccine, ProQuad® (which has a significantly
higher risk of serious adverse effects), and Merck’s shingles HVZ vaccine, Zostavax®, are factored
Currently, the Establishment is engaged in introducing vaccines, like Merck’s Gardasil® and
GlaxoSmithKline’s Cervarix®, with no proof of long-term effectiveness and self-generated, self-
serving “cost effectiveness”, which clearly ignore the costs to those who have had, are having and
will have serious adverse reactions
Furthermore, after their approval, the CDC immediately recommended mass vaccination
programs for these vaccines with almost no in-use proof of safety and no in-use proof of
effectiveness in preventing cervical cancer.
Worse, both the CDC and the FDA seem almost total indifferent to the hundreds of reported
vaccine-induced injuries as well as the tens of vaccine-linked deaths, which, quite predictably, the
Establishment attributes to mere coincidence.
In addition, the Establishment has introduced vaccines, like the current rotavirus vaccines,
that have clearly negative US cost-effectiveness (where the cost of the vaccination program far
Tellingly, before Merck’s Gardasil® HPV vaccine was introduced, Varivax consistently had the highest incidence
of adverse-event reports in the VAERS database in the 1990s and early 2000s.
exceeds the costs of the background level of rotavirus in the USA) and, for Merck’s genetically
engineered RotaTeq®, have clearly increased US rotavirus disease risk in those children and adults
who were previously “immune” to the native human rotavirus strains to which they have been
exposed during their childhood but are not protected from being infected by the genetically
engineered bovine-human hybridized viruses in Rotateq.
Moreover, the standards for licensing a vaccine in the USA have been reduced from the
vaccine: a) must be truly effective in preventing the disease in most of those who have been
vaccinated and b) must reduce the harm from the disease in those who are vaccinated and still
contract the disease as well as c) reduce the transmission of the disease to:
? In the case of the rotavirus vaccines, for the limited and biased clinical trials
conducted, the vaccines were approved based on a finding that the risk of the serious
harm caused by the vaccines is not statistically higher than the risk of harm caused
by the natural disease in the control population used in the phase-3 clinical trials.
? In the case of the human papilloma virus (HPV) vaccines, the vaccines were
approved based on claims that the vaccines may, in this instance, prevent some
vaccine-associated cervical cancers in some of the vaccinated women three to five
decades after they complete the initial 3-dose vaccination schedule, even though:
a. There is no proof that HPV infection causes cervical cancer — only proof that
HPV infection levels are associated with cervical cancer,
b. The “efficacy” data indicates a post-vaccination loss of efficacy in less than a
c. The strains of HPV in either vaccine (HPV types 6, 11, 16, and 18 in Gardasil
and types 16 and 18) are not even the major strains of the disease prevalent in
the USA – in fact the type 11 strain is almost non-existent (“0.1%”) in the US
d. The approvals are not questioned when the levels of adverse-event reports,
including serious maiming and death, currently far exceeds the level of the
other vaccines even though only a small percentage of the eligible population is
being vaccinated with these vaccines while the level of vaccination in most of
Dunne EF, Unger ER, Sternberg M, McQuillan G, Swan DC, Patel SS, Markowitz LE. Prevalence of HPV
Infection Among Females in the United States. JAMA. 2007 February 28; 297(8): 813-819.
The most common HPV types detected were HPV-62 (3.3%; 95% CI, 2.2%-5.1%) and HPV-84 (3.3%; 95% CI, 2.2%-
5.1%), HPV-53 (2.8%; 95% CI, 2.1%-3.7%), and HPV-89 (2.4%; 95% CI, 1.4%-4.3%) and HPV-61 (2.4%; 95% CI,
1.6%-3.8%) (FIGURE 2). HPV-16 was detected in 1.5% (95% CI, 0.9%-2.6%) of females aged 14 to 59 years. There
was no statistically significant difference in the prevalence of HPV-16 and the 13 more commonly detected types, except
for HPV-84 and HPV-62. HPV-6 was detected in 1.3% (95% CI, 0.8%-2.3%), HPV-11 in 0.1% (95% CI, 0.0 %-0.3%;
relative SE_30%), and HPV-18 in 0.8% (95% CI, 0.4%-1.5%) of female participants. Most participants infected with
HPV (60.1%) had only 1 HPV type detected (95% CI, 53.2%-67.9%); however, 23.9% had 2 types (95% CI, 18.3%-
31.3%) and 16% had 3 or more types detected (95% CI, 12.0%-21.2%). Overall, HPV types 6, 11, 16, or 18 were
detected in 3.4% of the study participants, corresponding with 3.1 million females with prevalent infection with HPV
types included in the quadrivalent HPV vaccine. Few participants (0.10%) had both HPV types 16 and 18 and none had
all 4 HPV vaccine types. At least 1 of these 4 HPV types was detected in 6.2% (95% CI, 3.8%-10.3%) of females aged
14 to 19 years.”
… Our data indicate that the burden of prevalent HPV infection among women was higher than previous estimates.
However, the prevalence of HPV vaccine types was relatively low”. [Emphasis added.]
the other vaccine programs that generate significant levels of serious adverse
events generally exceed 75 % of the population segments covered by the
5. “The Establishment’s Efforts To Increase Their Protection From Civil Lawsuits Are
Furthermore, through an appeal in Bruesewitz v. Wyeth being heard by the US Supreme
Court this Fall, the vaccine makers and the rest of the Establishment are essentially attempting to
have the Supreme Court rule that the 7th Amendment14 of the Constitution of the United States of
America, an integral part of the “Bill of Rights” reserved to the people of the United States of
America, does not apply to those who have suffered, or are the guardians of those who have
suffered, a vaccine-induced injury.
The artifice being used to carry this argument is that 42 U.S.C. § 300aa-22. Standards of
responsibility is an issue that can be decided once, and for all, by the judiciary, outside of a civil
trial by jury on the facts of each case.
This argument is being advanced even though, under the NVICP, the vaccine maker’s lack
of liability under § 300aa-22 is supposed to be the issue decided in the first phase of any vaccine-
related civil jury trial.
That such liability decisions belong to the trial jury is clearly set forth in § 300aa-23. Trial,
which at § 300aa-23(b), states:
The first stage of such a civil action shall be held to determine if a vaccine
manufacturer is liable under section 300aa-22 of this title”. [Emphasis added.]
Moreover, the Establishment’s arguments knowingly ignore § 300aa-22(b) with respect
“warnings”, in general, and § 300aa-22(b)(2), which states:
“For purposes of paragraph (1), a vaccine shall be presumed to be accompanied by proper
directions and warnings if the vaccine manufacturer shows that it complied in all
material respects with all requirements under the Federal Food, Drug, and Cosmetic
Act [21 U.S.C. 301 et seq.] and section 262 of this title (including regulations issued
under such provisions) applicable to the vaccine and related to vaccine-related injury
or death for which the civil action was brought unless the plaintiff shows – …”
? As the putative causative DTP vaccine in question is a Thimerosal-preserved vaccine
given to the child and
? The vaccine manufacturers have admitted knowingly failing to comply with Title 21
of the Code of Federal Regulations (21 CFR) as set forth in section 610.15(a) (21
CFR § 610.15(a)), which requires the level of preservative must be proven to be
“In Suits at common law, where the value in controversy shall exceed twenty dollars, the right of trial by jury shall
be preserved, and no fact tried by a jury, shall be otherwise re-examined in any Court of the United States, than
according to the rules of the common law”.
“sufficiently nontoxic so that the amount present in the recommended dose of the
product will not be toxic to the recipient”, in testimony given before a Congressional
committee which investigated the vaccine makers and the US Food and Drug
Administration’ actions from 1999 and which subsequently published a formal
Congressional report, “Mercury in Medicine – Taking Unnecessary Risks” in 200315
and the requirement in question is a material requirement under the Federal Food,
Drug, and Cosmetic Act [21 U.S.C. 301 et seq.] as well as a safety regulation issued
under the provisions in “section 262 of this title”16 [emphasis added],
the Wyeth defendant is clearly guilty of failing to comply “in all material respects with all
requirements under the Federal Food, Drug, and Cosmetic Act [21 U.S.C. 301 et seq.] and section
262 of this title (including regulations issued under such provisions) applicable to the vaccine and
related to vaccine-related injury or death for which the civil action was brought”.
Moreover, recognizing defendant Wyeth’s knowing and intentional failure to comply with
the black letter law, the US Supreme Court should, when it hears the case this Fall: a) find for the
Bruesewitz plaintiffs and b) take whatever actions needed to ensure that the Bruesewitz plaintiffs
are awarded appropriate punitive damages for defendant Wyeth’s knowing and willful failure to
comply with 21 CFR § 610.15(a) for the preservative Thimerosal in the vaccine that caused the
harm to the Bruesewitz child.
However, given the Establishment’s denial of reality of vaccine-induced mercury toxicity in
susceptible children, like the Bruesewitz child, who were, and are still being, given vaccines
preserved with Thimerosal (49.55% mercury by weight) and the power that the Establishment
wields, the people will be lucky if the US Supreme Court finds for the Bruesewitz plaintiffs.
Finally, should the US Supreme Court find for Wyeth, then, the people will most assuredly
know that both the Establishment and the US Supreme Court are knowingly severing those who
bring vaccine cases against the vaccine manufacturers in the legal manner provided by NVICP from
the right to a civil jury trial for damages that is supposedly guaranteed by the 7th Amendment to the
Constitution of the USA.
6. “The ‘Life Saving’ Annual Influenza Vaccination Program”
Factually, there is no scientific proof that the influenza vaccine prevents even most (> 50%)
of those who are “vaccinated” with an influenza vaccine from contracting and spreading influenza
during the “flu season” – none whatsoever (see, for example, Geier DA, King PG, Geier MR.
Influenza Vaccine: Review of Effectiveness of the U.S. Immunization Program, and Policy
Considerations. J. Am. Physicians and Surgeons 2006 Fall; 11: 69-74 [the only US-population-
See Finding 3, “3. Manufacturers of vaccines and thimerosal, (an ethylmercury compound used in vaccines), have never
conducted adequate testing on the safety of thimerosal. The FDA has never required manufacturers to conduct adequate safety
testing on thimerosal and ethylmercury compounds” (page 6), in May 2003, Subcommittee on Human Rights &
Wellness of the Government Reform Committee, US House of Representatives (Chairman Dan Burton – following
a 3 year congressional investigation), “Mercury in Medicine – Taking Unnecessary Risks” pgs 1-80 and, in
abbreviated form, published in the Extended Congressional Record: Subcommittee on Human Rights and Wellness,
Committee on Government Reform of the House of Representatives, “Mercury in Medicine Report,” Washington,
DC, as published in the Congressional Record, pgs. E1011-E1030, May 21, 2003
Here, “this title” is “TITLE 42 – THE PUBLIC HEALTH AND WELFARE” of the United States Code.
wide retrospective of in-use effectiveness evaluation – not model – for the influenza vaccination
programs in the USA for the years 1979 through 2001]); and other unbiased independent studies as
well as the independent reviews of the published studies (see, for example: Jefferson T, Di
Pietrantonj C, Rivetti A, Bawazeer GA, Al-Ansary LA, Ferroni E. Vaccines for preventing
influenza in healthy adults. Cochrane Database of Systematic Reviews 2010, Issue 7. Art. No.:
CD001269), which clearly show that the inoculation of populations with influenza vaccines, both
inactivated- and, more recently, live-virus, is not effective in preventing those who are inoculated
from getting “influenza” during the “flu season”.
Furthermore, there is some evidence that getting an influenza inoculation in one year may
increase the inoculated individual’s risk of contracting an influenza infection in a subsequent year
Additionally, a recent double-blind clinical trial study found that supplementation with
vitamin D-3 was much more effective in preventing influenza-type-A infections than influenza
vaccination (see: Urashima M, Segawa T, Okazaki M, Kurihara M, Wada Y, Ida H. Randomized
trial of vitamin D supplementation to prevent seasonal influenza A in schoolchildren. Am J Clin
Nutr. 2010 May; 91(5): 1255-1260. Epub 2010 Mar 10. PMID: 20219962).
Finally, as is usually the case, Establishment’s fear mongering and propagandizing carefully
hides the fact that influenza is not a highly contagious disease (see: Cannell JJ, Zasloff M, Garland
CF, Scragg R, Giovannucci E. On the epidemiology of influenza. Virol J. 2008 Feb 25; 5: 29 [Note:
Among the issues this electronically published review article addresses is the absence of any valid value for the sick-to-well infectivity for human influenza in spite of numerous attempts to determine even a valid estimate, which clearly establishes that influenza is not highly infective.]).
Thus, the Establishment is recommending mandates for various groups of people, and the
State of New Jersey is currently mandating, a non-effective vaccination program for a disease that is
not highly contagious on the grounds that, to say the least, this less-than-scientifically-sound, non-
effective prophylactic treatment, influenza vaccination, will somehow protect those who submit to it
from spreading a disease that it does not prevent them from contracting, and, when those inoculated
get the live-virus vaccine, a disease with which those receiving it not only are directly infected by
three strains of live viral influenza but have also been shown to shed the live virus for at least 21
days after being inoculated with said live-virus vaccine.
Furthermore, in spite of an ever-increasing body of evidence that vitamin D-3
supplementation is a more effective preventive for type “A” influenza than any influenza vaccine,
this Establishment continues to ignoring this proven and highly effective prophylactic use of
vitamin D-3, which protects all against contracting all strains of type “A” human influenza, instead
of suboptimal protection from getting the two (2) type A strains of flu in the flu vaccine.
Obviously, the Establishment’s recommendations and actions are not grounded in sound
science nor based on public health concerns; they are clearly driven by other imperatives.
7. “Medical Mandates Are Required For The ‘Greater Good’”
Whenever this author hears any group or zealot, including any vaccine apologist,
recommending that any person should surrender his or her right to make his or her own informed
medical decisions to some “higher authority” (be it employer, state or nation) “for the greater
good”, this commenter knows that the group or person advocating for such is a medical fascist17
who is seeking to take away our personal freedom to make medical choices for ourselves and those
for whom we are responsible and who is advocating for a “religious cult”, the cult of the “public
health” vaccinationists, who seek to mandate that all must sacrifice or risk sacrificing some aspect
of their own or their children’s health on the vaccine altar “for the greater good” – the good of the
Establishment – of which the group or individual demanding the surrender of the rights to informed
choice and consent is a well-paid member, who depends on promoting these sacrifices for his or her
status, position, and/or livelihood.
8. “Vaccines, the Safest of Prophylactic Healthcare Measures”
We are repeatedly sold the myth that “vaccines are the safest disease-preventive medicines”,
when the truth is that, as a group, they are the least safe of disease-preventive medicines (see: Neil
Z. Miller’s Vaccine Safety Manual For Concerned Families and Health Practitioners, 2nd
edition (2010), ISBN 978-188121737-4) and the only class of prophylactic medicines for which
there are no long-term safety studies and, increasingly, not true-placebo-controlled short-term large-
scale safety studies (in a vaccinated versus totally unvaccinated [using sterile isotonic pH-balanced
saline for the controls] with > 50,000 in each arm of the study).
In addition, instead of proof of effectiveness and long-term (lifetime [> 50-year protection])
effectiveness, we are given antibody-titer-based measures of claimed efficacy of limited duration
(typically, 10 years or less) for “most vaccines” after typically 2 to 5 inoculations for most
(typically, > 60%) of those who are initially inoculated multiple times, with a carefully concealed
reality that each such inoculation campaign kills a few18 who are inoculated and harms some
additional multiple of that number each year to varying degrees.
9. “Vaccines Do Not Cause Autism Or Any Other Chronic Medical Condition”
How much longer will Americans tolerate the increasingly obvious lie that the
Establishment’s vaccination programs are not a causal factor in ‘Autism’ and other chronic
childhood medical conditions that once were rare (< 1 to 2 instances in every 10,000 children) but
are now at epidemic levels (> 1 instance in every 10 to 1,000 children)?
How much longer will the American public continue to tolerate the epidemics of chronic
diseases; and epidemic rates of chronic disease that, for asthma, now exceed 10 % of our children
and, in the aggregate, have brought us to a nation where, in 2006, more than 25%19 of our children
have at least one chronic lifetime medical condition so that the Establishment may continue to grow
Defined here as any member of medical community who favors dictatorial medicine where all medical decisions
are under the control of the “medical police” and “medical courts”; and the individual has no rights to make his or
her own informed medical decisions without fear of any retribution, ostracism or oppression.
Based on the reality that vaccination accounts for most of our excess infant mortality rate over that infant mortality
rate in Japan in the first year of life, this “few” deaths per vaccination collectively translates to about 2 per 1,000
live births or about 8,000 – 9,000 newborn babies in the USA each year.
“The rate of chronic health conditions among children in the United States increased from 12.8% in 1994 to 26.6%
in 2006”. [http://www.medscape.com/viewarticle/717030?sssdmh=dm1.591574&src=nldne&uac=140083MY] [Note: 26.8/12.8 is about a
factor of 2.1 – without considering the increase in population of children by about 50% – making the population
percentage increase not 210 % but rather 300+ %.]
and profit at the expense of the increasing damage to the fiscal and physical health of ourselves and
How much longer will the American public be blinded by the propaganda spewed forth
daily by these servants of greed who have been and are knowingly sacrificing our health and
prosperity so that the Establishment they serve may continue to grow in size and profit while our
fiscal and physical health is stolen from us?
Even though this commenter cannot answer for those who read these questions, his past and
on-going efforts clearly point out the reality that he has lost his tolerance for the status quo and, with
eyes wide open, he is seeking to open the eyes of the public to the preceding realities and to march
with that informed and enlightened public to change the USA, not for the “greater good”, but rather
for a return to a system of laws in which the rights of every competent citizen are respected and
everyone has the freedom to freely choose, or reject, all prophylactic vaccination programs without
any penalty, stigma, or recriminations from those who do not share the same views.
In addition, this commenter is: 1) seeking to change the laws protecting the Establishment’s
vaccine purveyors from being held directly accountable for the harm their vaccine products cause
and the lack of safety and/or appropriate effectiveness of many of their vaccine products and 2)
hoping that, after reading this commentary, those who ‘get it’ will join with this commenter in
demanding: a) direct vaccine purveyor accountability and b) the absolute right to choose which, if
any, vaccination programs and when, if ever, the vaccines chosen should be administered – or,
simply, “opt in” vaccination laws in every State, which would repeal the current mandates and
eliminate any and all need for an exemption of any type from any prophylactic or other vaccination
About Paul G. King, PhD
Paul G. King, PhD Analytical Chemist, is a scientist who has studied both vaccines and
vaccination programs intensively for more than a decade and has sorted out the underlying science
to the extent that he could find such from all of the published information available from those with
differing views about vaccination and vaccination programs.
If any, after reading this article, any reader finds any significant error for which there is
unbiased science that clearly supports your alternative views, then, by all means, send your
alternative view or views and their supporting documentation to me through firstname.lastname@example.org and, if
your studies are truly unbiased, this author will be glad to: a) modify his views accordingly and b)
publish an updated article. If you find areas where the text has grammatical, spelling or word-
usage errors, please let the author know so that he may appropriately correct them and published a
revised version of this article.
For additional information about Dr. King and his interests, the reader can visit his
personal web site, http://www.dr-king.com/.