Natural Solutions Foundation Emergency Health Freedom Action eAlert
The Voice of Global Health Freedom™
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org

February 5, 2010 Permalink: http://www.healthfreedomusa.org/?p=4615

Dear Health Freedom Supporter,

This is an Emergency eBlast concerning the three serious emergencies we are facing right now, today:

Emergency #1. Health Freedom eAlerts Being Blocked!
Emergency #2. McCain Bill, S 3002, Implementing Codex for Supplements, Gutting Health Freedom Must be Stopped!
Emergency #3. GMOs contaminating our Food Supply! This must stop NOW!
Emergency #1:

 This text-only eAlert in an attempt to pierce  the wall of censorship that has become increasingly apparent blocking your Health Freedom Action eAlerts over the past several weeks. Ever since the ground breaking  2010 Health Freedom War Council our blasts are blocked, censored, and blatantly interfered with. We have recently been alerted that AOL, Verizon, Yahoo, Gmail and possibly other email service providers appear to be preventing our urgent messages from getting to you, our subscribers.  This despite the fact that emails are only sent is to supporters who have individually chosen to receive these messages, (”opted in”). Yes, Natural Solutions Foundation blasts are being blocked, in violation of your right to freedom of information!

Why?  Because we are truly the Voice of Global Health Freedom™ and we are very effective! You know you can rely on our information, and so do the Powers That Be, the ones that do not want you to have that information.  It really is that simple.

 When you receive this email, we urge you to send it to everyone you know since our ability to reach our huge email list is being blocked, we believe, intentionally.

This urgent note is from General Bert Stubblebine, the Natural Solutions Foundation President: “Mouse Warriors, we need your ACTION now! Please follow the plan we’ve put forward in this eblast. This is a long message, but we need you to follow it through. Your health and freedom are, quite simply, at stake!”

Emergency #2:

Sen.  John McCain has introduced a horrific bill, S 3002, the “Dietary Supplement Safety [sic] Act of 2010″ (DSSA) designed to end your access to high potency supplements by giving the bloated, corrupt and dangerous FDA MORE power to destroy supplement access.  This bill is  absolutely NOT to be confused with DSHEA, the Dietary Supplements Health and Education Act (1994), which says nutrients are food and, as food, you can have them in any form – and any amount – you like.  If we allow DSSA to pass, we will be living – and dying – under something very much like the European Food Supplements Directive’s anti-supplement restrictions, implementing Codex Alimentarius’ dietary supplements and nutritional restrictions, to the “T” — effective as close to immediately as the Fraud and Death Administration can manage it. Listen to the Dr. Rima Reports as Dr. Rima interviews Sarah Schones, MD, a German Immunologist practicing natural medicine in Germany: .  Food Supplements are going the way of the dodo in the EU.  The US is clearly next unless we act now – in massive numbers, once for each member of your family, at

http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=26714

Your legal right to access supplements and herbs will, quite frankly, be a thing of the past. As we predicted years ago, the end of the first decade of the new millennium was intended to be when we lost our Health Freedom. Will you let that happen?

For several years, the Natural Soluitions Foundation has kept you abeast of the battle for our food, our health, our freedom, indeed, as we documented and discussed in our 2010 Health Freedom War Council last month, our very lives.  We have predicted that the FDA’s Big Pharma Phriendly policies would bring Codex-style restrictions home to us as “safety” when, in fact, they are nothing short of health tyranny.

Once again, the Natural Solutions Foundation brings you the important stories — we warned you, within hours of McCain announcing his intent, that this was happening, http://vitaminlawyerhealthfreedom.blogspot.com/2010/02/mccain-bill-poses-threat-to-dshea-and.html.

We call upon you to act now!  By clicking here, http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=26714, you are joining those who have acted upon this important information and have begun to awaken the public to this threat. It’s time to move to ACTION.

Read more about this dangerous bill here - http://www.healthfreedomusa.org/?p=4608

Here is the Action item which you must take now, once for each member of your family, IF you value your health, your supplements and your freedom.

http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=26714

We are in active contact with our friends in Congress and with key opinion makers, seeking powerful alliances to stop the McCain bill and its companion “Food Safety [sic]” Bill, s510. It would appear that the ploy (you might call it a “conspiracy”) is to combine the two “Food Safety [sick] Bills into one, combining her worst features of each, of course.

We will keep you posted as the story unfolds, but there is literally no time to wait or waste.  This MUST be nipped in the bud so deeply that it never arises again! THIS IS WHERE PUSH BACK TURNS INTO TAKE DOWN!

McCain:  Pharma Tool, Globalist Fool.  But, as foolish as he may be, his bill poses a major threat to you right now! [Question: if pro is the opposite of con, does that mean Congress is the opposite of Progress?]

The only thing they listen to is numbers; we proved that when we Pushed Back with over 2.8 million emails, against the planned, mass, forced “Swine Flu” vaccine — and the threat evaporated. Let’s do it again! Let’s set a goal of 1 million emails to the Senate, 1 million emails to the White House and 1 million emails to HHS Secretray Seibelius, 1 million emails to the Senate “HELP” committe where the dangerous companion to McCain’s bill, S510, the (sic) “Food Safety Bill” has been stalled since our Push Back campaing in December, will be joined shortly by this latest assault on our freedom.

That’s a lot of emails, right?  Well, our email system allows you to send an email to your Senator, Pres. Obama, Sec. Sebelius and HELP committe chair Harkin with one click of your freedom mouse.

We need to innundate the Senate HELP committee, since Tom Harkin said in November, in response to the over 150,000 emails that we generated in one weekend, that  “DSHEA … governs the law here, not Codex standards…” and that the provision in S510 allowing FDA to “make recommendations including whether to harmonize with Codex does not signal any intent to move in a different direction on DSHEA…”

Now it’s time for Senator Tom Harkin to keep that pledge and stop the McCain Anti-DSHEA Bill!

See: http://www.healthfreedomusa.org/?p=4014 for Senator Harkin’s comments.
See: http://www.healthfreedomusa.org/?p=4608 for the dangerous terms of the McCain bill.

http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=26714

Emergency #3:

http://salsa.democracyinaction.org/o/568/p/dia/action/public/?action_KEY=2049

Why should you take the two Action Items above?

Why? Because your freedom depends upon it.  Sen. Mc Cain’s new bill will bring Codex to your supplement shelf – and make sure it is empty!

And here is my Open Letter to Forbes Magazine… about their pro-vaccine stance
Does it suprise you that Forbes named Monsanto as its Company of the Year?
http://www.healthfreedomusa.org/?p=4568

Please make your Tax Exempt recurring donation here, now.
http://www.healthfreedomusa.org/?page_id=189

That’s the full story, in two words.  Here are the other two words to the story: Try Them!

Dr. Rima’s Cognitive Enhancement Packs:
http://www.healthfreedomusa.org/?p=4558

Or our new Dr Rima Recommends Network link, www.DrRima.net

www.NaturalSolutionsMarketPlace.org

TUNE IN Every Week! Wednesday 8-10 PM Eastern

Think vaccine schedules are just for children? Think again!

Natural Solutions Foundation
The Voice of Global Health Freedom™
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org

I re-post in full the February 3rd media release from the Natural Products Association regarding new threats to health freedom.

It was Constitutionalist Dr. Ron Paul (R-Texas) who described the FDA’s behavior as “an abuse of power…” and now failed presidential candidate John McCain lets us know where he stands: on the side of the power abusers and against the Dietary Supplement Health and Education Act of 1994 (DSHEA) which a unanimous Congress adopted to protect our access to high potency nutrients. With the suppression of wholesome, natural nutrition and natural remedies will come the preventable diseases of mal- and under-nutrition, a lower population and profits along the way.

The “Accepted Dietary Ingredient List” in the McCain bill is an especially troubling provision since such a code provision moves us away from our Common Law Right to access the foods we choose to a Civil Law (Codex Alimentarius) regulation of what we may choose. Under the Common Law what is not explicitly forbidden is allowed; under the Code, whatever is not explicitly permitted is forbidden. This “lawyer’s distinction” is of the greatest significance in preserving our Liberty. This provision could outlaw thousands of herbs, minerals and nutrients, just as similar European provisions are limiting dietary ingredient choice under the EU’s implementation of Codex.

Action Item: http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=26714

The terms of this bill further the Globalist Eugenicidal Agenda (of the “Bigs” — Big Agribiz, Big Pharma, Big Finance, Big Govt…) in that they seek to treat dietary supplements, which are foods and therefore ought to be deemed safe if used as directed, as though they were toxins (while, of course, the agency treats the real dangers – GMOs, food additives, dangerous drugs, vaccines and industrial toxins as though they were perfectly safe). If they succeed, our best hope for safe foods and high potency nutrients could be gone.

Further, this bill needs to be seen in the context of the other fake “Safety” bill pending in the Senate, the The FDA Food Safety Modernization Act, S 510, which does “for” family farms and ranches, natural and community food production what the McCain bill does to dietary supplements: create restrictions that the “Bigs” can live with but which will drive ethical, local production out of the market. See: http://www.healthfreedomusa.org/?p=4014 for Sen Tom Harkin’s assurance this past November that DSHEA was not under attack. But now it appears to be under attack and we view McCain’s bill as part of a concerted effort to restrict Health Freedom. – RF

—————–
February 3, 2010: New Legislation Poses Threat to DSHEA

At a press conference held earlier today, Sen. John McCain (R-Ariz.) announced that he would be introducing legislation that would amend the Dietary Supplement Health and Education Act (DSHEA) to give the U.S. Food and Drug Administration (FDA) additional powers over retailers and suppliers in the dietary supplements industry. The Natural Products Association is reviewing McCain’s bill, which is cosponsored by Sen. Byron Dorgan (D-N.D.), and offers this initial analysis regarding the impact of the legislation on the industry.

NPA will work aggressively to address this threat to the industry. The association will continue to keep its members informed and let them know how they can help protect their businesses.

Brief description of the provisions of the Dietary Supplement Safety Act of 2010

New Requirements from Suppliers to Retailers

Suppliers and retailers regardless of size all along the chain of commerce are required to “obtain adequate written evidence” from the seller that the product is registered as required. That evidence must be retained in a file available for inspection.

Adverse Event Reporting (AER)

Requires reporting of all adverse events, not just serious adverse events. In addition, a compilation of non-serious AERs must be submitted annually, and records must be maintained for three years.

“Accepted Dietary Ingredients” List

Mandates creation by the Secretary of a list of “Accepted Dietary Ingredients” to replace the current “in commerce pre-DSHEA” test.

New Dietary Ingredients (NDI)

NDIs are considered adulterated unless there is a history of use or evidence of its safety. Registrants shall maintain a “scientifically reasonable substantiation file” available for inspection by the Secretary of Health and Human Services. Registration required 75 days prior to market.

Recall Authority

Provides immediate recall authority to the Secretary upon determination that a supplement “would cause serious, adverse health consequences or death, or is adulterated or misbranded.” Companies subject to a recall have the right to challenge the order in an “informal hearing” within 10 days. At their own expense, retailers must notify customers of such recalls.

Registration of Dietary Supplement Facilities

Dietary supplement facilities shall register with the Secretary (required information includes name, address of all facilities, trade names, list of supplements, their ingredients, and labels). Registration is annual.

Read the complete bill here:
http://www.npainfo.org/clientuploads/regulatoryLegislative/2010%20Dietary%20Supplement%20Safety%20Bill.pdf

This entry also posted at: http://www.campaignforliberty.com/blog.php?view=32204
And: http://vitaminlawyerhealthfreedom.blogspot.com/2010/02/mccain-bill-poses-threat-to-dshea-and.html

Natural Solutions Foundation
The Voice of Global Health Freedom™
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org

Dr. S Humphries MD is a physician of principle. A doctor who knows the first rule is Do No Harm. In recent months this physician has become sensitized to the risks of vaccination. The doctor was distressed to learn that hospital policy essentially forced patients to have vaccinations without doctor approval and without any meaningful informed consent. The good doctor objected. And the report continues with what happened next:

My dissatisfaction eventually made it to the Chief of Internal Medicine who challenged me to produce peer-reviewed journal articles in support of my objection. There were dozens of case reports of kidney disease or small blood vessel inflammation following influenza vaccination. In fact, one paper cited 16 patients in its written report(1). Under-reporting of adverse vaccine reactions is a known phenomenon. The National Vaccine Information Center estimates that only about two percent of adverse vaccine reactions ever get reported. It would follow that written and published case reports found in medical journals represent a miniscule sampling of the totality of vaccine injury cases. These implications should evoke at least some curiosity on the part of doctors and health care advocates.

The peer-reviewed literature was delivered to the department head. His initial response was to suggest that future vaccination orders be signed off by another physician so I didn’t have to be involved with the process of a nurse giving a “routine” flu shot. But the point had been missed; flu shots should not be given to sick patients.

I was challenging “routine orders” that had been in place since 2007. The defense for supporting the policy was that no side effects had been reported since the standing order had been instituted. I wondered to myself and then later inquired: How do you know that is true? Is it because nobody filed a formal report? If a patient became more ill after the shot, did you consider his condition to be a side effect of the vaccine, or was it simply called an unfortunate complication to the patient’s current illness? What if the patient was discharged from the hospital but readmitted several weeks later. Was the reason logged simply as a progression of his existing disease…or was the cause an overlooked, delayed side effect of the vaccination? If vaccine reactions are not considered as part of a patient’s differential diagnosis, how do you know? Without taking a vaccine history when considering a timeline of events, how could anybody possibly make the connection between a vaccine and a subsequent illness? How does anyone else know for that matter – that there were no side effects from the “routine” administration of flu shots, ordered by a pharmacist and given by a nurse, without doctor consent? The truth is, there is no real tracking and reporting system in place. And nobody is enthused about trying to start one. What has essentially happened is that the guards have all been told to go home and nobody is thinking to even look for the wolf.

Dr. Humphries continues with the report and with important information you need to consider if you or your loved ones have to interact with an increasingly distant, bureaucratized and uncaring “health care” delivery system, including the following:

Be vigilant and ask questions. Big Pharma has dozed past another barrier and now its reach has expanded past your doctor and right into your hospital room. Propaganda about vaccines and the flu will be posted around the hospital. If ever there was a time to become highly suspicious of the motives in the world of hospitals and pharmaceutical business, it is now. Take these suggestions to heart:

* When somebody other than your doctor enters your hospital room and offers you anything, even if they tell you the doctor ordered it, do not believe that you must accept it without first talking to the doctor in charge of your care. You have a right to know why you are being injected and what the risks are.

* If there is ever a good time to get a vaccine, it is not while you are sick. Please consider both sides of the vaccination debate before agreeing to one. You won’t be given a fact sheet with balanced pros and cons by a conventional medical doctor or by the hospital.

* You have the right to refuse any drug, any shot and any intervention at any time, as long as you are psychologically competent.

You can read the full report at: http://www.medicalvoices.org/vaccination/articles/vaccination-without-doctor-approval-in-a-us-hospital.html

Ralph Fucetola JD
Natural Solutions Trustee
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org

Natural Solutions Foundation
The Voice of Global Health Freedom™
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org

”

To the Editor, Forbes Magazine:

Your recent plea to make sure that everyone lines up for an H1N1 vaccination relies on misinformation, shocking in a publication which prides itself on reliable, research-based articles.

You decry the “pseudoscience” of the “vaccine deniers” and state that failure to get vaccinated was probably the cause of many of the deaths which you uncritically ascribe to a lack of vaccination.

Your breathless endorsement of inaccurate propaganda requires a fact-based response –

First, your assertion that H1N1 has “taken 14,160 lives, 2,328 of them in the U.S. Within the latter group are 248 children” is dramatic, but meaningless and totally inaccurate.

According to the CDC, FDA and WHO, the tests available to determine whether someone has H1N1 are wrong 90% of the time. Allegedly because of the total uselessness of tests, WHO, CDC and FDA advised health systems and nations to STOP TESTING for H1N1 and simply assume that any illness or death related in any way to respiratory difficulties was caused by H1N1.

WHO and CDC advised countries to stop testing for H1N1 on July 10, 2009. CBS released the results of a 3 month investigation on October 29, 2009 which confirmed that laboratory testing was incorrect 90% of the time when a determination of H1N1 infection was made. Thus, there is no clear evidence that anyone has, in fact, either “gotten” or “died from” this virus.

It is accurate to state that case numbers and deaths are ascribed to the H1N1 virus, but there is no evidence to support either. I would hesitate to accuse Forbes of disseminating misinformation, but it certainly is misinformation to present a number of cases and deaths without making clear the fact that these numbers have literally no basis in fact.

You state that many of these [putative] Swine Flu deaths could have been prevented by vaccination. This, too, lacks a single shred of scientific evidence. In fact, the antibody titers assumed to be present following H1N1 vaccination have never been documented to relate to any level of protection. No US or international agency has ever conducted published studies documenting that these antibodies are in any way related to disease protection. All the propaganda detailing the urgent necessity to receive this vaccination stands on the emptiest of pedestals: in fact, the fact that neither safety nor efficacy testing has been done on this vaccine, supposedly required to protect the world against a grim Level 6 pandemic threat, is the reason that the Natural Solutions Foundation, www.HealthFreedomUSA.org and www.GlobalHealthFreedom.org, has initiated legal action against the FDA, CDC, etc., to prevent the deployment of this untested, unnecessary and potentially dangerous vaccine.

Although the virus is presented as “novel”, springing suddenly into existence near the factory swine farms of Mexico, and causing its first alleged death in Mexico City on April 14, 2009, Novartis’ Swine Flu vaccine was recalled in February 2009. Baxter and other pharmaceutical companies applied for patents to manufacture vaccines for a virus which supposedly did not exist starting in 2007.

I would strongly suggest that your publication run a story on the psychics employed by Big Pharma to guide their industrial decisions.
You repeat the story that the vaccine grew slower than expected and account for the “shortage” of doses in this way. Logically speaking, if Novartis’ Swine Flu vaccine was subjected to a recall in February, 2009, then at least those doses hot recalled would have been available and, although they are untested, as all other H1N1 (and, indeed, all influenza) vaccines are, they were available.

In fact, widely available data show convincingly that the shortage of vaccine doses was nothing more than a marketing ploy to spur vaccine sales, acknowledged in a tape recorded, and widely disseminated, Council on Foreign Relations meeting on October 26, 2009.
This widely trumpeted “shortage” was propagated by constant media coverage. Perhaps your investigations into purported vaccine shortage might have revealed another widely known data bit: Rupert Murdoch’s son, and heir apparent, James, is the Chairman and Chief Executive of News Corporation for Europe and Asia. James is an overseer of GlaxoSmithKline’s Board of Directors. Not only is GSK a major H1N1 vaccine manufacturer, its vaccine was withdrawn because the death rate from its use in Canada was twice the expected rate.

Expected vaccine death rate? Again, your research might have provided your readers with the FDA’s estimates of anticipated best-case adverse reactions. Published on their website, they declared that the anticipated number of deaths following H1N1 vaccine administration was likely to be 1 in 100,000. With a US population of roughly 310 Million, that calculates to a best case scenario of 31,000 needless deaths in the US alone from the untested, unnecessary and uninsurable H1N1 vaccine, assuming universal vaccination, as HHS and DHS announced was their goal on July 24 and 25, 2008, respectively, in identically worded Advisories. These Advisories, considering the weaponized, laboratory-created Avian Flu, stated that it was the goal of the United States to vaccinate “every man, woman and child in the United States, starting with those who want it first.”

The evidence that the Avian Flu and H1N1 viruses are man-made is overwhelming. A single piece of data will suffice for this communication: the genetic sequence of the 1918 “Spanish Flu” was nowhere to be found on earth until Dr. Jeffery Taubenberger succeeded after a 6 year effort, funded by the National Institutes of Health, in decoding that sequence from viruses isolated from the frozen lungs of an Inuit Eskimo victim.

Thus, the fact that the pathogenic (disease causing) genetic sequence now exists in both the H5N1 Avian Flu virus and the H1N1 Swine Flu virus is, to any rational mind, highly probative that both of these viruses are, in fact, weaponized agents.

Agents of what? Well, perhaps of greed.

The United States took the unprecedented steps of -

1. Purchasing nearly 1/2 Billion dollars of injectible squalene in preparation for injection of this deadly substance, known to create incapacitating autoimmune destruction of mammals in even tiny doses and never approved for injection PRIOR to the approval of any H1N1 vaccines

2. Purchasing the entire stock of 5 different H1N1 vaccines intended for injection in the US PRIOR to the approval of any H1N1 vaccines

3. Announcing its plans to vaccinate every child and pregnant women in the United States PRIOR to any safety testing or efficacy testing of any of its purchased vaccines (to the tune of about $7 Billion)

4. Announcing its approval of 5 vaccines which it had purchased for use at 90,000 administration sites

5. Declaring that these vaccines were merely “change of strain” vaccines despite the fact that -

a. They were made by novel means against a novel virus with characteristics unlike any every seen before, according to FDA, CDC and WHO

b. They were designed to combat a virus whose origins reputable scientists were declaring to be from intentional laboratory manipulation

c. There was no evidence that the influenza vaccines, from which the H1N1 vaccine was a mere change of strain variant, were either safe or effective, given that numerous peer reviewed articles in major medical journals like the New England Journal of Medicine documented that children who receive flu vaccines are many times more likely to be hospitalized for all causes, be on medication for asthma, eczema and other immune problems and suffer other serious medical problems for their entire life spans

d. mercury free doses were not widely available so that children receiving the recommended number of flu shots and H1N1 shots would be receiving hundreds of times the [already horrifyingly inflated] “maximum safe dose” of mercury.

Furthermore, the FDA granted vaccine manufacturers total immunity from any proximate or long term damage caused by their products unless they were guilty of “willful negligence”.

One might suspect, of course, that the irrational rush to deploy these untested vaccines might be due to a wish by the financially compromised, linked, share holding and otherwise conflict-of-interest-rich regulators to protect vaccine manufacturers from anything that could pierce that veil since only after safety testing was completed (scheduled for July, 2010), could willful negligence be charged if dangerous vaccines were deployed.

Of course, another intention might be to create a continuing market share since vaccinated persons are the ideal customers for the pharmaceutical industry: they have life-long chronic diseases, including cancers, autism, diabetes and other immune system and neurological illnesses, in far greater numbers than non-vaccinated persons, study after study shows.

Pandemic prediction has become an exact science according to epidemiologists: merely examine the patterns of vaccination programs.

Whatever disease, in whatever population, is vaccinated “against” develops into an outbreak, epidemic or pandemic.

Considering the history of vaccination, probably the greatest medical scam in history, that is not really surprising.

Jenner, the artificially revered “father of immunization” was, in fact, a mountebank who purchased his medical degree for 25 lbs from the University of Edinburgh without ever having attended a single medical class.

He “published” the results of his inoculations of healthy people with the pus from open “cowpox” lesions from the hands of milkmaids despite the fact that re-vaccination led to multiple fatalities from what we now would call “anaphylactic shock”.

Those reactions were in the fortunate few, however. The unfortunate many developed syphilis since there is no such thing as “cowpox” – Jenner was making a direct inoculation into his victims of live, infective syphilitic spirochetes.

After the British Parliament had made small pox vaccination mandatory for infants, an epidemic of normal infants dying of syphilis provoked a full scale investigation into Jenner and his techniques. At that time, Jenner was receiving a life stipend of 10,000 pounds per year.

The Parliament was faced with a serious problem: either reveal that it had been duped and had, inadvertently, caused the incurable illness and deaths of huge numbers of British Citizens or construct a cover-up.

The latter course of events seemed preferable and Jenner’s stipend was doubled to 20,000 pounds per year.

The vaccination mandate was continued in the British Empire.

In the tropics, however, where the medical influence of the Empire was making itself felt, there were no cowpox lesions to be had.

Instead, it was decided that the open sores of lepers would provide the materials necessary to “protect” babies, children and adults against smallpox. This decision, like the original decision to mandate vaccination, was made in the total absence of any scientific evaluation.

The result was a horrifying epidemic of iatrogenic leprosy in the tropical portions of the British Empire.

Thus, an industry, and a deception, was born.

Your discussion of the “complex regulatory hurdles” set by the FDA against the use of adjuvants is similarly incorrect.

In fact, the nasal vaccine, produced by Medimmune™, does not have adjuvants. All other H1N1 vaccines approved by the FDA have them: aluminum, for example, which is designed, like all adjuvants, to save the manufacturers money since the antigen is the expensive part of a vaccine. Using an immune system irritant [i.e, an adjuvant] means that higher antibody titers can be obtained with less antigen per dose.

All adjuvants are toxic to the nervous system and the immune system. Aluminum, for example, is a heavy metal with known significant neurotoxicity.

The adjuvant which was not approved for use is squalene, also known as “Freund’s Complete Adjuvant”, used in laboratory settings to destroy the immune protection in an animal that keeps the immune system from destroying itself and its “host”. Squalene is a normal component fatty molecule of the nervous system. It is also a compound used safely in cosmetics, fragrances and foods. Only when it is delivered to the body in an injected form is it dangerous. And then it is very, very dangerous since it causes the body to “break tolerance” or recognize itself as not to be attacked. Once tolerance is broken, any and all auto immune phenomena can take place with every tissue being attacked by its own immune system.

Injections of tiny amounts of squalene in the notorious “Vaccine A”, to which military members in Gulf War I were exposed, supposedly to protect them against anthrax, led to the devastating and frequently fatal “Gulf War Syndrome” which afflicted nearly 700,000 US troops.
Squalene has been turned down by the FDA for testing in its injectible form several years before the H1N1 vaccines. The letter notifying the drug company of the refusal to allow it to be tested made it clear that it was “too dangerous to be accepted for testing in the United States at this time”.

Two patents filed in 1998, however, make it clear that injected doses of squalene approximately 1 million times larger than that injected in Vaccine A recipients would cause an immune-mediated infertility which could never be reversed.

Why would that be attractive to vaccine proponents?

WHO declared a Level 6 Pandemic on June 11, 2009. In order to do so, it had to change the definition of a Pandemic . Instead of a novel organism which could spread easily and cause significant disease and widespread death to which people did not have general immunity, now any organism could be designated a Pandemic organism and rapid escalation from Level 4 (which still required significant disease and death capabilities) to Level 5 and then Level 6 followed once that change was made.

In fact, although the first alleged death in Mexico occurred on April 14, 2009, and not one confirmed death had occurred in the US from H1N1, a US “Health Emergency” was declared on April 25, 2009, a mere 11 days later. That is awfully quick to isolate a novel virus and determine its ability to create a pandemic.

The US, you recall, purchased nearly $500,000,000 worth of squalene for admixture into H1N1 vaccines, but even their own scientists would not sign off on its use, according to the Congressional testimony of HHS Secretary Sebelius in her September 15, 2009 testimony before the US Senate.

Instead, she informed them, through an Emergency Use Authorization, that store of squalene would be admixed at 90,000 injection sites around the country where people were expected to obediently follow your advice and “just get vaccinated”.

Interestingly, the immune-mediated permanent infertility turns out to be of enormous potential interest to the WHO since they espouse:

1. A sustainable planet

2. A necessary reduction of the population of the planet to 10% of its current level (yes, you read that correctly)

3. The use of vaccines, like the ones they have been researching and deploying, according to their own literature and documents, since they began their Special Commission on Infertility Vaccines in 1974.

WHO was convicted by the Philippine High Court of sterilizing more than 3 million Philippine women involuntarily in their “tetanus” vaccination campaign there.

WHO announced in its own documents that the purpose of the supposed smallpox eradication campaign in Africa was “to eliminate 150 million excess Sub-Saharan Africans.”

WHO’s population reduction agenda matches precisely the explicitly stated and formally adopted one of the United States. Henry Kissinger, then Secretary of State, authored National Security Memorandum 200 for then-President Richard Nixon. In that now-declassified document he asserted that “Population reduction must be the primary goal of US Foreign Policy.”

WHO, like the Federal Reserve Board, is a private corporation duty bound to meet the needs of its shareholders and funders.

Although WHO was, at its founding, to have been funded by the member states it was to serve, it receives more than 2/3 of its funding directly from pharmaceutical companies.

Those funders are the beneficiaries of WHOs insistence upon the use of vaccines, which are hugely profitable when used in great numbers, but not profitable at all when their use is minimal.

You state that the FDA regulators are timid.

This does not conform to any data of which I am aware. Regulators approved the needless and wildly dangerous Rotovac injection despite documented connections between vaccination and the development of epilepsy and death from pneumonia. Regulators accept stock, stock options, grant money and other benefits and make decisions that imperil the public at large on a daily basis.

The problem is so bad that scientists who work for the FDA and make recommendations which the regulators routinely boldly ignore in deference to their own self interest (and a conflicted interest it is!) wrote to President Obama upon his election pleading with him to rein in the deadly FDA regulators.

No such reigning has taken place.

The very definition of “conflict of interest” has been vitiated so that there is, in essence, no such thing any longer.

It would be helpful if FDA regulators WERE timid.

There is good reason that aspirin (which kills 1500+ people every year) would not qualify for approval today. It may be commonly available, but it is a dangerous compound, causing hearing loss, kidney damage and bleeding in huge numbers of people. Tylenol is responsible for approximately 800 cases of Acute Liver Failure and at least 450 deaths per year and polio vaccine, like every other vaccine, has yet to be proven either safe or effective by a placebo controlled, double blind study. In fact, the CDC lists the administration of polio vaccine as a significant cause of polio, a disease whose causative agent has never been isolated according to Koch’s postulate and which, despite the best propaganda efforts of the vaccine industry, appears to be a chronic environmental toxicity, not a viral disorder at all.

Your final ’scariest’ reason for the apparent, although not real, shortage of H1N1 vaccine is that people insisted on single dose vials which, unlike the multiple dose ones, contain no thimerosal, a compound which contains 49.6% mercury by weight.

Perhaps a brief review of the history of mercury in vaccines would be useful to you.

What is scary is that the FDA has ever permitted mercury in vaccines.

Shortly after the FDA was created, when it was in the process of compiling its GRAS, or Generally Regarded as Safe, list, Eli Lilly applied for approval of Thimerosal on that list.

There had already been a number of products which contained mercury whose ingestion had been shown to be deadly or, if not immediately deadly, then damaging to the nervous system of the ingestor. Baby teething products containing mercury and mercurochrome, for example, were well known to be tremendously toxic. But the “preservative” thimerosal was profitable for Eli Lilly so they were willing to fight for it.

Eleven patients with meningitis who were already in coma were given injections of thimerosal. All of the patients died. Eli Lilly reported out the test as indicating that the substance was safe since all 11 “would have died of other causes anyway”.

The FDA accepted this shameful excuse for science and began a cover-up of nearly 80 years duration to pretend that mercury is a safe substance.

In order to meet the FDA’s guidelines for a safe daily exposure, an infant getting flu shots would have to weigh 650 lbs. To meet OSHAs’ requirement, it would have to weigh 6500 lbs. Most infants fail to meet those safety requirements.

Vaccinations have increased more than exponentially. When I was in medical school, from which I graduated in 1970, using the same diagnostic criteria, the rate of autism was between 1 and 4 children per 10,000. Today the rate is between 1 child in 69 (New Jersey, the most heavily vaccinated state in the US) and 1 child in 100.

Genetics are to blame for the increase, we are told. Genetics degrading by 100 fold in 40 years? Hardly. “Ah”, some say, “But when mercury is removed from vaccines, as in Denmark and Japan, the rate of autism continues to rise.”

“Ah”, we answer, “The amount of mercury retained when bottles are washed with Thimerosal in order to “prevent mold” is still significant. And it is clear that mercury is the heavy metal neurotoxin most related to the biggest number of cases of autism, but it is hardly the only toxin the brain encounters in vaccines.”

No, the only way to eliminate these devastating neurological disorders is to eliminate vaccines. Will we miss them? Well, Big Pharma will. But people who do not make money from illness will not.

After a broad-brush ad hominim attack trashing anyone who does not adhere to the vaccine mantra, despite its total lack of scientific validation (making it, in fact, pseudoscience) the author pulls out the final stick in his bundle: herd immunity.

There is, scientifically speaking, absolutely no such thing. As a candidate for pseudoscience, “herd immunity” is a real comer.

Vaccinations are alleged to protect the immune system of an individual by inducing antibody preparedness and “training” the immune system to produce antibodies rapidly if it meets the injected antigen again. If those antibodies were the same as naturally occurring ones (and, of course, if the very process of immunization did not damage the immune and neurological systems of the vaccinated person), the effect would be personal. Keeping the infecting organism out of the group/herd environment, as herd immunity is supposed to do, is irrelevant to antibody production. If vaccines work, they work on an individual basis.

The US vaccination rate is far higher than the requisite 90% which experts tout as necessary for this effect to take hold. But we still have outbreaks of diseases against which people have been vaccinated. Why?

If herd immunity were a reality, the slope of the decline in diseases like hepatitis B and small pox would not have begun to decline before the introduction of the vaccine and would certainly not have continued to decline at precisely the same slope after the introduction of the vaccines for that disease, nor continued, again, at precisely the same slope, after the achievement of herd immunity levels of “protection”.

Texas recorded a 41% increase in chicken pox cases in children between 2005 and 2006 despite the fact that every child entering kindergarten was vaccinated against chicken pox.

What herd? What immunity?

College campuses with 97% of students having received 2 mumps vaccine injections were among those whose students were part of a 2006 mumps outbreak. Of a total of 6584 confirmed and probable cases of mumps reported to the CDC in that outbreak, the bulk occurred on college campuses in 9 Midwestern states with near total immunization.

What herd? What immunity?

In the Czech Republic, children receive 2 doses of MMR. A 2005 outbreak showed the highest incidence among those who had received both shots.

In 1986, 90% of 1300 Pertussis (Whooping Cough) cases in a Kansas outbreak were in appropriately vaccinated persons.

In Norway and Denmark in 1998, an epidemic of Whooping Cough occurred in a population with a nearly 96% vaccination rate.
Of 479 Whooping Cough cases in the United States during a 1982 outbreak, 60% of the recipients had one or two doses of the DPT vaccine, while the other 40% had been fully vaccinated.

What herd? What immunity?

There are those parents of autistic children, like the author of your piece, who continue to believe in vaccination. That is their right.
They may respond rationally or irrationally when their belief is challenged. That is their right.

But a publication of the stature and seriousness of Forbes Magazine needs to exercise more restraint and probity.

While the holy dogma of vaccine effectiveness serves the Church of Pharmaceutical Medicine, it is, like all dogma, merely a matter of faith, one might say, of pseudoscience, because there is no real science behind it. None. There is real money and real propaganda, but there is no science behind it.

The contempt of your author may be understandable as the wail of a parent in pain who has not yet found the cure for his child’s autism, but it has no place in your magazine. Unless, of course, your shareholders are served by pharmaceutical success on the broken bodies and brains of our young, who will never be your readers because the vaccines you tout have destroyed their nervous systems.

Yours in health and freedom,
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org

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