The weaponization of this world continues as the globalist elite continue their campaign to “cull” the human population through the genome-destroying technologies of nuke power, GMOs and the toxins found in environment, drugs and especially vaccines. Here Dr. Rima discusses some of the latest vaccine atrocities.
Dr. Rima’s Dispatches from the Vaccine Wars:
Vaxocrats know the deal: Vaccines are neither safe nor effective, as they must be under the laws governing them in the US. That makes, according to my understanding, EVERY vaccine used in the US an illegal, improperly registered and approved drug. What’s new here is that the unreliability of the DPT vaccine has been confirmed by the CDC itself. … read the whole article below.
CDC Vaxocrats Know DPT Cannot Be Trusted! Now You Know It, Too!
Not Safe, Not Effective and CDC Knows It!
Dr. Rima’s Dispatches from the Vaccine Wars:
Vaxocrats know the deal: Vaccines are neither safe nor effective, as they must be under the laws governing them in the US. That makes, according to my understanding, EVERY vaccine used in the US an illegal, improperly registered and approved drug. What’s new here is that the unreliability of the DPT vaccine has been confirmed by the CDC itself. The good news is that this is important data to help us spread the wisdom of refusing ALL vaccines. The bad news is that I predict that it will be used to mandate useless and dangerous DPT vaccines in an every-three-year-booster schedule. No: don’t trust the Vacocrats!
No: don’t accept vaccines, an uninsurably risky behavior!
No: don’t accept vaccine mandates!
Yes, Take Action Here: http://salsa.democracyinaction.org/o/568/p/dia/action/public/?action_KEY=5708m (http://tinyurl.com/noforcedvax) and forward this link to everyone you know so they can do the same!
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I post here my Certification in support of a petition for Habeas Corpus on behalf of one of the prisoners of conscience in the United States, Jim Folsom of the San Diego area. Jim’s “crime?” Providing frequency devices to consenting adults, none of whom ever complained about the devices they bought! More about his story below.
I find myself bemused by what I was about to type describing his trial and conviction by a “Jury of his Peers.” I was about to describe the trial as an “economics-crime political show-trial” when I realized that a couple decades ago I would have (and did) describe the judicial process in the old Soviet Union that way, as the party-in-power sought to retain power at all costs, as its society collapsed under the weight of central economic planning. Here in the USA the central planners already control the finance system and are working overtime seeking to control health and food (hence, we seek Health and Food Freedom!).
It is a very sad commentary on America that the parallels to the now-happily-gone USSR and the overbearing central authorities of the USA become unavoidable… and, I believe, symptomatic of the last gasp of a dying tyranny. But along the way, decent people like Jim and his wife Sata suffer. This leads me to recommit to the struggle for Liberty. Without Freedom, we will be nothing but ciphers in a deadening world…
The Writ of Habeas Corpus (Latin for “Bring me the Person”) is practically the last remaining of the Common Law Writs (near all others having been “superseded” by the Civil Action form). The Great Writ, as it is called, remains because it is protected by a clause in the Constitution. It provides a way to challenge incarceration on the grounds that the conviction or continued holding of the Person violates fundamental rights. – Ralph Fucetola JD
Here is the draft of the Certification in Support of Habeas Corpus
Ralph Fucetola JD declares under penalty of perjury pursuant to 28 U.S.C. 1746 that the following information is true to best of my knowledge and belief and that if called to testify in this matter I could testify competently to these facts and opinions. This Certification is made to support the issuance of a Writ of Habeas Corpus under 28 U.S.C. 2241(a) in that the Petitioner has been convicted and confined in violation of the Constitution and Laws of the United States.
1. I practiced law from 1971 through 2006 in the State of New Jersey; thereafter I have provided professional legal consultation services to the natural products and nonmedical devices industries. I am a Notary Public of the State of New Jersey, Notary No. 2398815.
2. In the course of my practice and consultancy I had occasion to meet James Folsom and to counsel and consult with him regarding the nonmedical device he offered. I provided consulting services and written opinions for the Defendant, and when he was indicted, I provided an expert opinion pre-trial report. I was not called upon to testify at the trial although I was prepared to do so and expected to do so.
3. Upon information and belief, at the time Defendant began to provide the device an Operations Manual that he had not written was available. This was the Manual that had been prepared as part of an Investigative New Device application. I was asked to advise regarding changes needed to update the Manual and make sure that it did not communicate in such a way as to suggest that the device was a medical device.
4. I also provided my opinion that under section 360(c) of the Statute the device, when properly presented with claims that did not include claims to diagnose, prescribe for, treat or cure medical conditions, did not require registration under the Statute. Although in general devices “intended for human use…” were subject to registration, the law and regulations provides exceptions that applied to the device.
5. In addition to that opinion, it was also my opinion that it is possible to qualify devices for “significantly equivalent frequency device” status under the “grandfather clause” of the May 28, 1976 Cosmetic, Food and Drug (Devices) Act (1976 CCFD Act).
6. From my review of the trial information, it appears that the primary FDA Agent testifying for the Government’s case during the trial denied that such a device exists. Interestingly, while this denial was/is going on, and as a corner-stone of the Prosecution’s “closing rebuttal” was trial photo Exhibit # 600 revealing just such a predicate – 1976 ‘grandfather clause’ device. The Prosecutor certainly did not know what was revealed in that photo, a photo that appears to have been taken April 2, 2003 showing the interior of Folsom’s storage unit with all the property and devices, including the “predicate” one, that were seized during the FDA raid against his business and property. That predicate device is now apparently located at the FDA’s Headquarters evidence room, San Clemente, California. And, significantly the FDA clearly implies no such device exists, although it does, or at least did exist.
7. The record shows the Prosecution, under Court Order, in 2008, as part of “pre-trial discovery,” to allow Folsom and his attorney (at the time) complete access to all evidence, and very specifically that evidence held at FDA Headquarters, San Clemente. “Partial” access and discovery was made in the summer of 2008, however, no discovery access to the devices, device components, accessories, manuals, documents, etc., that were shown in the trial photo Exhibit # 600 was made available by the Government/FDA at this evidence room. This access and discovery was denied, even after “court admonishments” toward the Prosecutor because of the intentional “delays and obstructions” that blocked partial and complete discovery. This appears from the record.
8. I am further aware that frequency programs and device technology (offered by another), was “grandfather clause” FDA 510 (k) accepted in June 2007, as a TENS device for “pain and muscular relaxation.” The Scanar device, developed from the Russian space program and the Scio devices, both providing frequencies, were FDA 510 (k) approved/accepted as “bio feedback devices. Restrictions do apply (similar to those experienced by the Food Supplement industry) in the marketing of these devices and what can be stated to the customer as regards frequencies as they relate to specific conditions and body functions. What is essential is a Disclaimer that there is no intent to “treat disease” but rather that the devices may offer therapies that may benefit. This is the advice I gave the Defendant and he forthwith directed that all suggested changes be made to the Operations Manual to include appropriate Disclaimers.
9. Such devices, in general, including the device herein, do not require 510(k) approval. Generally, devices “intended for human use…” must be registered, with certain exceptions, stated in the statute:
(l) Exemption from reporting requirements – A report under subsection (k) of this section is not required for a device intended for human use that is exempted from the requirements of this subsection under subsection (m) of this section or is within a type that has been classified into class I under section 360c of this title. The exception established in the preceding sentence does not apply to any class I device that is intended for a use which is of substantial importance in preventing impairment of human health, or to any class I device that presents a potential unreasonable risk of illness or injury.
Furthermore, the statute provides a definition of Class I devices:
(A) Class I, General Controls… (I) is not purported or represented to be for a use in supporting or sustaining human life or for a use which is of substantial importance in preventing impairment of human health, and (II) does not present a potential unreasonable risk of illness or injury…
10. It is my understanding that the device herein is not “for a use in supporting or sustaining human life or for a use which is of substantial importance in preventing impairment of human health, and… does not present a potential unreasonable risk of illness or injury…” The intent of the device is provision of pre-diagnostic evaluation for self-education and research purposes, to achieve and maintain a status of wellness, not to prevent impairment of human health, nor does such a device present any potential risk of illness or injury; it is the equivalent of a battery-powered, micro-amp device. It is not intended to “treat” disease but rather to provide the body with biologically compatible energy or to provide a therapy that may benefit.
11. Government acknowledgement of the existence of a “predicate” device allows FDA “acceptance” under Sec. 360 of the 1976 CCFD Act -“grandfather” clause (for “medical device” or complete “exemption”). Meaning for a device to receive FDA acceptance under the 1976 CCFD Act “grandfather” clause there would be no requirement for the multi-million dollar expenses and time consumption for “double-blind” studies, etc., only the pharmaceutical companies can afford. This cost is only one of the many impediments and restrictions preventing pharmaceutical industry competition. This is the reason also no manufacturer within the device industry can afford or comply with the normal FDA 510 (k) requirements – it is impossible and therefore the “underground” element to get a low cost alternative health care modality out to the American people. There is no “level playing field” in existence between “Complementary and Alternative Therapies,” vs. “Allopathic/ Pharmaceutical Medicine.” It simply does not exist.
12. Currently, without use of the 1976 CCFD Act “grandfather” clause, all manufacturers within the device industry, would be required for FDA 510 (k) acceptance, to apply over and over again for each applicable body “health and wellness” or “medical” condition (for hundreds, if not thousands of conditions if each were applied) for man or animal. The costs and processes would be prohibitive. However, if it can be officially acknowledged and accepted that there exists a 1976 “predicate” device, then the path to regulatory acceptance would be open. A major efficacious low cost “health and wellness” frequency modality would then readily be made – “out in the open and not underground anymore” available to the American people.
13. Besides the device industry, past discrediting took place against other “alternative healing modalities.” The Chiropractic industry experienced the same until winning a major court case in 1991. The “food supplement” industry was fending off the unwanted encroachments of the FDA until the supplemental DSHEA Act was brought about as a compromise – sponsored by Senator Orin Hatch in 1994. Acupuncture, recognized in the Orient for thousands of years, was finally accepted by main stream medicine as one of the “healing arts” here in the U.S. in 2001 as a result of a leading Federal Court case arising in Texas.
14. There is a regulatory category of product or service in which these various modalities, including device technology, clearly fit that excludes them from the practice of medicine and thus from being medical devices or services. That category is what may be termed “therapies that may benefit” as opposed to “treatment of disease.”
15. The Code of Medical Ethics of the American Medical Association has also begun to acknowledge an independent use of the term “therapy” to describe non-medical health care services.
16. While “treatment which has no scientific basis” remains condemned (Opinion 3.01), under Opinion 3.04, physicians are free to “refer” a patient “for therapeutic or diagnostic services to another physician, limited practitioner or any other provider of health care services permitted by law to furnish such services, whenever he or she believes that this may benefit the patient.” Thus, unscientific “treatment” is distinguished from “health care services permitted by law.” “Treatment” — which means the use of standard medicine and surgery to “cure” disease — is distinguished from other health care services (therapies) which need only meet the lesser “may benefit” standard.
17. While physicians “prescribe” treatments for disease, therapies that may benefit may be subject to “referral” thereby further indicating the distinction. Thus, for example, energetic devices that support normal structure and function, even to support therapeutic outcomes, can be seen to complement licensed medicine, but not to be part of it, or held to its strictures, nor limited in its practice to licensed physicians. This is the essence of the case of Andrews v Ballard (USDC, TX, 498 F Supp 1038, 1980) is cited as a leading authority for the propositions that (1) a decision to obtain (in this case) acupuncture needle therapies from one not licensed as a medical doctor is a constitutional right encompassed by the right of privacy (p.1048) and (2) the provisions of the medical practices act, insofar as they limit the use of acupuncture needles to licensed physicians, are unconstitutional (p.1051, et seq.). This and other cases recognized a Federally protected right to access information about unlicensed products and services.
18. In the case involving this Defendant, an old Operations Manual that he did not author was shown to the jury but the revised Manual that he authorized was not, thereby depriving the Public of access to information about unlicensed products and services.
19. See also, Thompson v. Western States Medical Center – 01-344, decided on April 29, 2002 – 535 U.S. 357 where the Court said,
“If the First Amendment means anything, it means that regulating speech must be a last – not first – resort… We have previously rejected the notion that the Government has an interest in preventing the dissemination of truthful commercial information in order to prevent members of the public from making bad decisions with the information… Even if the Government did argue that it had an interest in preventing misleading advertisements, this interest could be satisfied by the far less restrictive alternative of requiring … a warning that the [product] had not undergone FDA testing and that its risks were unknown.”
20. Thus, since such therapies are not prescription services, members of the public may choose such services without the permission of their physician and as of right. That right is beyond FDA authority to prohibit, based on First Amendment Expressive Association interests.
21. In the case of State v Biggs (46 SE Reporter 401, 1903) the North Carolina Supreme Court dealt with a person who was advising people as to diet, and administering massage, baths and physical culture. In the Biggs case, the defendant actually “advertised himself as a ‘nonmedical physician’…[and] held himself out to the public to cure disease by ‘a system of drugless healing’…” p.401. That Court held that there could be no “state system of healing” p.402 and while
“Those who wish to be treated by practitioners of medicine and surgery had the guaranty that such practitioners had been duly examined…those who had faith in treatment by methods not included in the ‘practice of medicine and surgery’ as usually understood, had reserved to them the right to practice their faith and be treated, if they chose, by those who openly and avowedly did not use either surgery or drugs in the treatment of diseases…” p.402.
Biggs was acquitted.
22. In this Defendant’s case, the Jury was not given the opportunity to understand the distinction between the “treatment of disease” which is a predicate for a device to be a “medical device” and “therapies that may benefit” which include such well-known modalities as acupuncture and biofeedback and some lesser known modalities such as energetic devices.
23. Under these circumstances, Justice would be best served by considering Jim Folsom’s age and returning him to his home, under such restrictions as might be deemed to protect the public, but not to restrict his private expressive association activities which are beyond the lawful purview of the Federal government. Defendant should be released forthwith as he is being punished for acts which could not be criminal under any reasonable interpretation of law. This matter is an exceptional case where the prisoner can show that his remedy is “inadequate or ineffective” and either the conviction should be voided, or he should therefore be permitted to be resentenced and released.
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OCTOBER 14, 2010 Mark Your Calendars! Dr. Rima Reports – Sunday Mornings!
Join us for your morning lift… on Dr. Rima’s Coffee Clatch This week: Mark Lerner – Stop Real ID Coalition http://stoprealidcoalition.com/
First, A Word From Our Sponsor:
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WE ARE BEING SERIOUSLY HACKED AND ATTACKED – AGAIN!
WHY? BECAUSE OUR PUSHBACK IS WORKING AND THE POWERS THAT BE ARE NOT AMUSED! “We are NOT Amused!”
This is the second time I have written this blast tonight. When I pushed “Save” a few moments ago, the whole blast disappeared. Is that an attack? I don’t know, but keep reading to find out what the indisputable attacks look like today alone:
Here’s what Patrick, our computer guy, wrote to me in today’s report about why our links are not working and we can’t log in to our sites – and, often, neither can you:
“1. Fake donations are logged into the site which we have to spend time and effort sorting out from the real ones, and which we have to pay for as bad charges. Two years ago, this cost us over $10,000 when our bank account was invaded and the “charges” taken from from our account.
2. We have several problems with our sites ‘going missing’, meaning that one day we have the site and the links work correctly but the next day we don’t. See below to understand more of how that is happening.
3. Our Site Hosting was changed against our will and without our knowledge or permission
4. All Security Logs and Access Records were cleaned out, as in ‘the archives were wiped out’. These archive are our security records of who has accessed the site, which means that all of the records of who went into what file and did what to it – are now gone.
5. The Password to our main hosting and domain service was changed without our knowledge or wish
6. Someone changed all our name servers so that the site would not display properly.
While it is possible that this was merely the result of a poor setup, I don’t think this was an accident. We use the services of several different companies and all of them have been attacked in the ways I am describing. The items that were changed would have to have been done by someone with access to our systems, and with knowledge of who else we had web services through.” [Note from General Stubblebine: not necessarily: if the incursion is at a high level, there is no need to assume that someone knows our passwords and therefore can do this sort of damage. In fact, if NSA or high-level corporate espionage is involved, this type of incursion would be very, very easy for them.]
Patrick goes on to say, “Note: By ‘Web Services’ I mean Hosting, Domain Names, File Storage, Email, and the like.
7. The Healthfreedomusa.org site, on which I have been working, was hacked OR Cracked. There was no major damage done, that I can tell, but there was damage. Several files were deleted, some pictures, and some links were messed up making it harder for us to get products to the people who order them and to help people navigate to our other pages. These incursions are nothing that can’t be fixed, but are a definite time, money, and energy drain.”
Why is this happening? Because we are winning and the other side is running scared. That’s why our nearly 800,000 emails on S. 510, S. 3767 and GMOs to the Senate are so important.
Clean Phude? Phude Safety? Give the FDA more power so they can “protect” us? Take a look at what they are doing with the power they already have and ask yourself if giving an agency that says IN COURT that you do NOT have a right to eat food you want MORE power is OK. If not, then taking action against S. 510 and S. 3767 are imperatives for you.
“In the thirty years of Morningland Dairy operations NO ONE has become ill from consuming their products. Yet they have been ordered by the Missouri Milk Board to destroy ALL of their cheese without actual tests being performed on the cheese stock. This is nearly 50,000 pounds of cheese, or approximately $250,000.
Since the Milk Board and the FDA showed up at Morningland on August 26th, they have been “embargoed” from shipping or making any product. They dumped their milk for nearly six weeks before being approved to send it into homogenized, pasteurized distribution. All the while, they have had to pay the bill to keep the dairy and cheese plant operational….”
That’s why our visits to their offices when we come in groups, armed with the talking points, are so very important. That’s why viralizing the Action Items (see above) and the Talking Points (see below) is so very, very, important.
OF COURSE they are attacking us! If you were the Uber Cartel and the other side were this successful, wouldn’t you attack them this way if you had no scruples and no desire to see anything like freedom for anyone but yourself?
We can only take this level of attack as a powerful confirmation that we, you and the Natural Solutions Foundation, are exerting a meaningful force against globalization, genocide and the contamination of our food! And that is why we cannot let up!
Yesterday I was a guest for 3 hours on the Mike Chambers Show. Literally every time I began to speak in-dept about the intentional contamination of the US food supply and the genocidal underbelly of this plan, or about vaccinations and their part in the genocide, the connection was lost and Mike was on the show by himself. Listen here, http://www.oraclebroadcasting.com/archives.php?stream=/midnightrider/midnightrider.2010-10-13_16k.mp3, to decide for yourself if it was random or regulated. Much the same thing happens in our Dr. Rima Reports show every Sunday morning from 10 Eastern Time to 1 PM at www.OracleBroadcasting.com or to listen with live chat, www.HealthFreedomPortal.org.
When we talk with Mark Lerner, a leading advocate against the Real ID biometric version of state intrusion this Sunday, October 17, we’ll see if the same thing happens!
Frankly, Let’s Be Clear About Something:
The Natural Solutions Foundation cannot operate without your support. Right now, half way through the month of October we do not have enough funds to go to the Codex Committee on Nutrition and Foods for Special Dietary Uses meeting in Chile early in November. What that means is that you will be, where Codex is concerned, blind and deaf. Your eyes and your ears, Gen. Bert and I, will not be there bringing you the real scoop, not some watered down, balsaamic happy nonsense. But to get there, we need your support. Now.
We need your recurring donations and coffee orders now
Free Introductory Webinar: Healthy Lungs the Chinese Way with Angela Malek
Experience Angela on line. She’ll be your Seminar Leader for the extraordinary Five Elements Week at the Valley of the Moon’s Natural Solutions Center Jan. 9-15, 2011 in Panama!
To invite others to join this free introductory webinar, copy and paste everything below into your invitation.
Topic: Healthy Lungs the Chinese Way
Date: Friday, October 15, 2010
Time: 9:00 pm, Eastern Daylight Time (New York, GMT-04:00)
Meeting Number: 730-911-781
Meeting Password: lungs
To start or join the online meeting go to https://naturalsolutionsfoundation.webex.com/naturalsolutionsfoundation/j.php?ED=138661352&UID=489018037&PW=NMmZkYWZmMDli&RT=MiMxMQ%3D%3D
Photo of a ginger flower at the Valley of the Moon™Restaurant
There are a number of reasons, all of them good ones, that I can think of.
Here are some of them, in no particular rank order:
1. You are interested in finding out more about the Natural Solutions Foundation’s Valley of the Moon™Eco Demonstration Project and how it might fit your needs. You have visited www.NaturalSolutionsFoundation.org and www.MyValleyoftheMoon.org and you are intrigued. Of course, you are welcome at any time but you might want to join Trustee Ralph Fucetola and a group of people for their next visit here (tentative dates: January 19 – 27, 2011). Contact us at firstname.lastname@example.org, subject PANAMA, for more information.
2. You know that the US is in the process of seizing both IRAs and 401s and “guaranteeing” them with the “strength” of the US Dollar to provide you with an “annuity” of 3% interest and you are not at all happy with this option. You know that you can still place your retirement funds offshore and are seriously considering this option.
3. You want to live in a community of like-minded people with a secure, BeyondOrganic food supply, natural medical center and other services and you want to do it outside the US.
4. You want to help to reclaim the production of clean, unadulterated food around the world through your support of, and connection with, the Valley of the Moon Eco Demonstration Project in Volcan, Panama. You don’t have to be a farmer to do so!
5. You want to attend our outstanding seminars and workshops, like Angela Malek’s “Living, Eating and Healing with the 5 Element Theory” Workshop from January 9 – 15, 2011. Watch a short video with Angela here: http://www.youtube.com/watch?v=RKmOB6VdctQ to get the “flavor”. Interested? Contact us at email@example.com with “5 Elements” as your subject line. More information: http://drrimatruthreports.com/?p=7035 — Space is strictly limited!
6. You love good food and the idea of reclaiming its production. You love eating it, too, and you can’t wait to eat at our gourmet organic restaurant!
7. You want to volunteer your time and talents at the Valley of the Moon! Again, use our firstname.lastname@example.org address with “Volunteer” in the subject line.
The Supreme Court is grappling with the question of how much protection the 1986 National Childhood Vaccine Injury Act was meant to provide vaccine manufacturers against lawsuits. The case involves Hannah Bruesewitz, whose parents claim that a Wyeth-manufactured D.T.P. vaccine she received as an infant in 1992 led to developmental problems. At issue is whether Bruesewitz’s parents should be allowed to sue Wyeth on the premise that the drug maker could have offered a safer vaccine but opted not to do so. The case has moved from the “vaccine court” to the Pennsylvania state court to federal court; Wyeth has thus far prevailed.
Actelion Pharma Failed To Report 3,500 Deaths
The same FDA which has chosen to believe that more than 3500 in utero deaths following H1N1 vaccination, up from 7 potentially flu-related spontaneous abortions in an average year, is insignificant and therefore does not constitute a significant increase worthy of safety responses, says that 3500 unreported deaths by Actelion Pharma IS significant. Noting that doctors under report drug and vaccine reactions by about 97%, the agency says “we do not agree that a determination of a relationship between Traceable use and death by 3 percent of healthcare providers who did respond to Actelion is insignificant. And the agency adds that there is no suggestion that healthcare providers “who did not respond to Actelion did not also believe there was…a relationship” between death in individual cases.
Findings Damaging to Drugs Suppressed, Drug Ineffective
October 14, 2010 — Data from industry-sponsored trials published in peer review journals are misleading the public about the safety and efficacy of their drugs, according to 2 reports published online October 13 in the British Medical Journal (BMJ).
In a meta-analysis that looked at all of the published and unpublished data on the antidepressant reboxetine (Pfizer) for the short-term treatment of major depression, investigators concluded that the drug was not only ineffective but also potentially harmful.
They also report that 74% of the data on patients who took part in the trials of reboxetine were not published because the findings were negative and that the data that were published about reboxetine overestimated its benefits and underestimated its harm.
“This meta-analysis provides a striking example of publication bias, in which the previously favourable risk-benefit profile of reboxetine shown in published trials is reversed by the addition of unpublished data,” Beate Wieseler, MD, deputy head of the Department of Drug Assessment at the Institute for Quality and Efficiency in Health Care, Cologne, Germany, told Medscape Medical News.
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Every Sunday 10 AM to 1 PM Eastern Time
We’re getting ready to return to Federal Court for the next round of the Stop the Shot Case. Last year your Push Back stopped mandated vaccines and the planned Swine Flu pandemic; your support let us go to Federal Court to challenge the FDA’s approval of the “novel” virus, but unsafety-tested, vaccine and the states that were mandating the vaccines backed off.
This year the Swine Flu virus has been added to the seasonal flu vaccine and we’re heading back to court. This year’s Complaint is stronger than last year and challenges ALL influenza vaccines. But to make it to court we must raise substantially more funding.
To donate, please go to http://drrimatruthreports.com/?page_id=189#StS
Please don’t forget the universal remedy, Nano Silver, www.Nutronix.com/naturalsolutions
And supplementing with Cognitive Enhancement Nutrients to keep your brain healthy and focused… this message from our friends at Biologics Nutraceuticals, providers of the Cognitive Enhancement Nutrition:
“Please let Health Freedom supporters know they can take advantage of our Double Dip Sale with $4.99 Economy Shipping to the entire US! All of the Dr. Rima Packs are discounted 10% with the additional option to buy 2 and get another pack of the same type added to your cart at checkout for free! You may also buy three of the same type individual bottles and receive a free bottle of the same type in your cart at checkout!”
Yours in health and freedom,
The Trustees of the Natural Solutions Foundation
Maj. Gen. Albert N. Stubblebine III (US Army, Ret.)
President – www.FoodFreedomeJournal.org
Rima E. Laibow, MD
Medical Director – www.DrRima.net
Ralph Fucetola, JD
Counsel and Trustee – www.NaturalSolutionsFoundation.org
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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 email@example.com 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/.
PUSH BACK! THEY TELL US IT CAN’T BE DONE. THEY ARE WRONG!
Save Food and Keep It Safe NOW! Take Action here to protect food from the dangerous fake “Food Safety Bill”, S. 510 which could be passed in the Special Session of Congress or in September. This is an urgent danger and we need your help. This is a new Action Item so even if you have registered your opposition to this bill before, please do so now by clicking here: http://drrimatruthreports.com/?p=6269. Now send this to all of your contacts asking them to take action and send it along for similar push back.
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PUSH BACK! LET’S HEAR IT FOR PUSH BACK! AND THEN, LET’S HAVE A WHOLE LOT MORE OF SAME.
Using the Courts, the Court of Public Opinion, Political Pressure, Radio and TV, Video Action Items in the Health Freedom Action eAlerts and similar publications, We, The People, are, in fact, exerting our power. We do not win every battle, but we win and win and win when we push together. This time, the victory is the reversal of a clearance for a dangerous GMO to be grown without restraint or supervision.
Children are among the major consumers of sugar. Sugar beets are among the major sources of sugar. Genetically modified sugar beets are adapted to survive the use of deadly chemicals. That is, in fact, despite the propaganda and hype, the only reason that most GMOs are created: to create an after market for deadly chemicals. Of course, the sales of GMO seed help the bottom line along for the Uber Cartel but the real money is in the increased use of, and subsequent sale of, the profitable chemicals which the same companies make. Oh, yes, of course they are also drug companies so they get you coming into the food cycle and the hospital when they sell you drugs for the conditions and diseases which their chemicals and dangerous GMO “foods” cause you to develop.
And, then there is the lack of safety information on consuming GMOs. All independent science makes it clear that there is no reason to believe that GMO foods are safe since their consequences are to damage the DNA OF EVERY CELL IN THE BODY, including the cells of children still unborn. All this, of course, without oversight by the FDA or USDA.
Do you know what happens when people eat genetically modified sugar? No? Neither do I. But when mammals eat GMO soy, their offspring die, or are born stunted. Their fertility is impaired, their GI tracts and kidneys and immune systems are impaired, too. So is just about every other part of their bodies. It stands to reason, of course, since the DNA and its dangerous products have never existed before and we simply lack the mechanisms to get rid of them once they are in our bodies.
Then there are super weeds and super pests and genetic contamination and…. well, it sort of makes sense to feed them to children if you are a genocidalist AND a drug company owner, don’t you think?
We rejoice that approval for GMO sugar beets was vacated (e.g., canceled) pending an environmental impact statement. But it was not vacated on the grounds that these products, once genetically modified, are unstudied, unsafe, unnecessary and must be stopped before they literally contaminate every plant and animal on earth in what is heading toward the greatest cataclysm in the history of life on this planet.
VICTORY! FEDERAL COURT RESCINDS USDA APPROVAL OF GENETICALLY ENGINEERED SUGAR BEETS
ORDER BANS PLANTING OR SALE OF CONTROVERSIAL CROP. COURT DENIES MONSANTO REQUEST TO ALLOW CONTINUED PLANTING
Today Judge Jeffrey White, federal district judge for the Northern District of California, issued a ruling granting the request of plaintiffs Center for Food Safety, Organic Seed Alliance, High Mowing Organic Seeds, and the Sierra Club to rescind the United States Department of Agriculture’s (USDA’s) approval of genetically engineered “Roundup Ready” sugar beets (Center for Food Safety v. Vilsack, No. C08-00484 JSW [N.D. Cal. 2010]). In September 2009, the Court had found that the USDA had violated the National Environmental Policy Act (NEPA) by approving the Monsanto-engineered biotech crop without first preparing an Environmental Impact Statement. The crop was engineered to resist the effects of Monsanto’s Roundup herbicide, which it sells to farmers together with the patented seed. Similar Roundup Ready crops have led to increased use of herbicides, proliferation of herbicide resistant weeds, and contamination of conventional and organic crops.
In today’s ruling the Court officially “vacated” the USDA “deregulation” of Monsanto’s biotech sugar beets and prohibited any future planting and sale pending the agency’s compliance with NEPA and all other relevant laws. USDA has estimated that an EIS may be ready by 2012.
Andrew Kimbrell, Executive Director of plaintiff and co-counsel the Center for Food Safety, stated, “This is a major victory for farmers, consumers and the rule of law. USDA has once again acted illegally and had its approval of a biotech crop rescinded. Hopefully the agency will learn that their mandate is to protect farmers, consumers and the environment and not the bottom line of corporations such as Monsanto.”
Paul Achitoff of Earthjustice, lead counsel for the plaintiffs, commented: “Time and again, USDA has ignored the law and abdicated its duty to protect the environment and American agriculture from genetically engineered crops designed to sell toxic chemicals. Time and again, citizens speaking truth to power have taken USDA to court and won.”
In his order, Judge White noted that USDA’s “errors are not minor or insignificant, and his “concern that Defendants are not taking this process seriously.” He also pointed out that “despite the fact that the statutes at issue are designed to protect the environment,” USDA and the sugar beet industry focused on the economic consequences to themselves, yet “failed to demonstrate that serious economic harm would be incurred pending a full economic review….”
The Court held in part:
…the Court GRANTS Plaintiffs’ request to vacate APHIS’s decision to deregulate genetically engineered sugar beets and remands this matter to APHIS. Based on this vacatur, genetically engineered sugar beets are once again regulated articles pursuant to the Plant Protection Act. This vacatur applies to all future plantings…
This is the second time a Court has rescinded USDA’s approval of a biotech crop. The first such crop, Roundup Ready alfalfa, is also illegal to plant, based on the vacating of its deregulation in 2007 pending preparation of an EIS. Although Monsanto took that case all the way to the Supreme Court and the High Court set aside part of the relief granted, the full prohibition on its planting – based on the same remedy granted here, the vacatur – remains in place. In the past several years federal courts have also held illegal USDA’s approval of biotech crop field trials, including the testing of biotech grasses in Oregon and the testing of engineered, pharmaceutical-producing crops in Hawai’i.