Archive for the ‘Vaccines’ Category

Paul Joseph Watson
Prison Planet.com
September 28, 2009

The testimony of a woman who claimed she was part of a military drill in California centered around setting up roadblocks to check if people had received the H1N1 vaccine has potentially been validated with another report of a swine flu checkpoint near San Diego.

Earlier this month we reported on the You Tube video of a woman who claimed to have taken part in an Army exercise which involved setting up roadblocks and checkpoints so authorities could check who has received the swine flu vaccine. Those who have had the shots will be fitted with an RFID bracelet so they can be tracked. Those who have not taken the shot will be offered it there and then and if they still refuse, will be carted off to an internment camp, according to the woman.

Former Kansas state trooper Greg Evensen spoke of similar checkpoints recently, when he told an audience in West Virginia that preparations to enforce mandated vaccinations were being focused around preventing those who haven’t had the shot from traveling.

“I have been told by state troopers across the country that there are plans ready to be implemented that would include roadblocks and choke points as we call them, major interstate junctions around major cities and so forth where the greatest number of people can be held until they prove their vaccination by papers,” Evenson said, adding that permanent RFID bracelets would then be used to identify those who had taken the shot.

“I have been told that the plans would include buses standing by for people at roadblocks that refuse to take the inoculation,” added Evenson, saying that such refusniks would then be taken to military bases and imprisoned.

“Get your shot or get on the bus, that’s what’s coming,” warned Evenson.

Authorities in Boston have already trialed RFID bracelet technology, with the purpose of creating a “vaccination map” charting which people have taken the vaccine and which have not, or “creating a citywide registry of everyone who has had a flu vaccination,” as a Boston Globe article describes.

Participants were given a bracelet with a unique identifier code, exactly as described in the You Tube clip of the woman’s testimony.

We have now received yet another report of a roadblock staffed by armed military personnel centered around checking whether people have received vaccines.

A reader e mailed us a photo (see top of page) and the testimony of his friend who was traveling from California to Arizona after visiting friends. The man was driving through mountains east of San Diego when he came across a roadblock.

“As I neared the border they had a checkpoint set up but not the usual stateline checkpoint,” he writes.

“As I approached I noticed armed military personnel had most of the cars pulled over and there were a lot of people going in and out of a mobile trailer. The people looked confused and some upset. Seeing what was going on made me really nervous,” the man adds.

He was then approached by a women in military fatigues who asked him where he was driving and “something about a vaccination.”

“I got scared and told her I was a state geologist doing field research and because I was doing so much driving back and forth I had my vaccine on campus. She didn’t say anything for a few seconds and then the car behind me started honking and she got pissed and waved me on. I was so scared!,” he concludes.

The truck with the green stripe seen in the image is undoubtedly a border patrol car, but a blow up of the picture shows men dressed in military cammo, not the usual single color green uniform of border patrol agents. One of the men on the left hand side of the car in front appears to be carrying a large firearm.

Whether this was just another of the sprawling internal checkpoints that are now popping up all over the country is open to debate, but the fact that vaccines were mentioned indicates that this was potentially another drill in preparation for a mass swine flu outbreak. The addition of mobile trailers and unhappy people being forced to leave their cars and undergo some form of involuntary procedure hints that this could have been something even more ominous.

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Jeffry John Aufderheide
VacTRUTH
September 14, 2009

See for yourself the study presented at the end of article. Please spread the word and make this go viral… no pun intended. Kindly reference and link to VacTRUTH!

Trials for the experimental H1N1 Swine flu vaccine commence Tuesday, September 15th in Thornton, Colorado. Novartis, a bio-pharmaceutical company that manufactures the vaccine,  is recommending that children participating in the trial receive two doses of an experimental vaccine which contain ingredients found in spermicides, cleaners, and cosmetics along with thimerosal and squalene (MF59). Everyone should have a sense of concern as the only safety checks for these children are a few blood draws and follow-up phone calls. No neurological testing. No kidding.

Official opinions from federal agencies, such as the CDC, insist that the new vaccine will be safe and effective. Experts say we can trust the new H1N1 experimental vaccine because the technology used to create the vaccine is time tested. Experts argue that the only variable changing from the ‘normal’ flu vaccine and the H1N1 experimental vaccine is the novel A/H1N1 antigen. In other words, the same vaccine ‘technology’ is used but with the new virus.

However, this is the furthest thing from the actual TRUTH. As will be demonstrated, the following information was obtained through enrolling a family member into the study to gain an understanding as to what the ingredients would be.  After finding out the the information I am about to share, enrollment in this trial has been canceled.

SETTING THE STAGE ON SAFETY AND SQUALENE (MF59)

I met with the research coordinator for the study along with Dr. Melamed, an immunologist conducting the study. Dr. Melamed altruistically shared his knowledge answering questions concerning immunology and the technology behind the vaccine while remaining evasive on questions of what was in the vaccine and legal ramifications if harm was done. Dr. Melamed reassured me several times that the experimental H1N1 vaccine was created just like past vaccines and that the technology was well established.

Requests for package inserts for the ingredients of the experimental H1N1 vaccine were denied on the grounds that this was a study and that information is privileged. However, we can still piece together some of the ingredients based upon the parental consent form.

“MF59 is an adjuvant which is used in influenza vaccines licensed for the adults and/or elderlyin many countries worldwide, but it is not contained in any vaccines currently approved in the United States.” (page 2)

Isn’t it interesting that the study states it is licensed for adults and elderly? This study is designed for children between the ages of 3 and 8 and they plan on shooting up newborns and pregnant women with this stuff? Buyer beware.

Here is what the World Association for Vaccine Education had to say about Squalene (MF59):

Squalene:C30H50 an Adjuvant

Too dangerous for human use, Squalene is not licensed for use in the United States.  Oil adjuvants like squalene have been ordinarily used to inflict diseases in animals – for experimentation and study.  According to anthrax vaccine expert Gary Matsumoto and other reliable sources, the US military used an unlicensed, experimental anthrax vaccination laced with squalene, with disastrous consequences, including Gulf War Sydrome. Chemical descriptions:
Unites States National Library of Medicine: PubChem
http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=638072

Toxicity:
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?CMD=search&DB=pubmed&term=%22Squalene%2ftoxicity%22[Mesh%20Terms%3anoexp

Adverse effects:

http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?CMD=search&DB=pubmed&term=%22Squalene%2fadverse%20effects%22[Mesh%20Terms%3anoexpMust read:
Matsumoto, Gary.  Vaccine A; The Covert Government Experiment That’s Killing Our Soldiers – and Why GI’s Are Only the First Victims. Basic Books, 2004.

Present in these vaccines:
Anthrax (experimental, used on military personnel)

Dr. Sherri Tenpenny also elaborates on the deleterious effects of the Squalene Adjuvant in a 2006 article entitled, “FLU SHOTS AND THE NEW ADJUVANTS: BEWARE!” and can be found in its entirety here. An excerpt from Dr. Tenpenny’s article can give a better appreciation and understanding of what squalene is capable of in the body…

“On first blush, squalene seems like a good choice for an adjuvant. Manufactured naturally in the liver, squalene is a precursor for cholesterol. In addition, squalene can be purchased at health food stores in its more commonly known form, “shark liver oil.” However, ingested squalene has a completely different effect on the body than injected squalene. When molecules of squalene enter the body through an injection, even at concentrations as small as 10 to 20 parts per billion, it can lead to self-destructive immune responses, such as autoimmune arthritis and lupus.

Several mechanisms have been proposed to explain this reaction. Metabolically, squalene stimulates an immune response excessively and nonspecifically. More than two dozen peer-reviewed scientific papers from ten different laboratories throughout the U.S., Europe, Asia, and Australia have been published documenting the development of autoimmune disease in animals subjected to squalene-based adjuvants. A convincing proposal for why this occurs includes the concept of “molecular mimicry” in which an antibody created against the squalene in MF59 can cross react with the body’s squalene on the surface of human cells. The destruction of the body’s own squalene can lead to debilitating autoimmune and central nervous system diseases.”

“Carcinogenicity, we (Dr. Deborah Novicki of Novartis, another pharmaceutical company) have done no testing for the carcinogenicity of MF59 adjuvant or any of our preventive vaccines. We haven’t done it and we don’t plan to.”

This information is found on a workshop on adjuvants and adjuvanted preventative and therapeutic vaccines hosted by the FDA. This gem of a quote is on page 391.

STRANGE BEDFELLOWS: THIMEROSAL AND SPERMICIDES

Further down we see that, while not mentioned explicitly as ingredients, one can deduce they are in the vaccine via an implied allergic reaction.

“If your child has had an allergic reaction in the past to eggs, egg products, neomycin or polymyxin (antibiotics), sodium ethylmercurothiosalicylate or thimerosal (compounds containing mercury that are frequently used as preservatives in vaccines), beta propriolactone (substance that inactivates a virus), or nonoxynol 9 (substance commonly used in cleaners, cosmetics, andspermicides), you must tell the medical staff…” (pg 8) (emphasis mine)

Thimerosal has been thoroughly exposed as a neurological toxin largely in part and much gratitude to Lyn Redwood who obtained the meeting minutes from a secret meeting between government officials and pharmaceutical companies discussing the effects of the mercury additive. The document is called the Simpsonwood document and details exclusively the neurological harm thimerosal causes in children. Dr. Russell Blaylock has a commentary on the document here or read the meeting minutes yourself  here.

“the number of dose related relationships [between mercury and autism] are linear and statistically significant. You can play with this all you want. They are linear. They are statistically significant.” – Dr. William Weil, American Academy of Pediatrics. Simpsonwood, GA, June 7, 2000

“the issue is that it is impossible, unethical to leave kids unimmunized, so you will never, ever resolve that issue [regarding the impact of mercury].” – Dr. Robert Chen, Chief of Vaccine Safety and Development, Centers For Disease Control, Simpsonwood, GA, June 7, 2000

“Forgive this personal comment, but I got called out at eight o’clock for an emergency call and my daughter-in-law delivered a son by c-section. Our first male in the line of the next generation and I do not want that grandson to get a Thimerosal containing vaccine until we know better what is going on. It will probably take a long time. In the meantime, and I know there are probably implications for this internationally, but in the meanwhile I think I want that grandson to only be given Thimerosal-free vaccines.” – Dr. Robert Johnson, Immunologist, University of Colorado, Simpsonwood, GA, June 7, 2000

“But there is now the point at which the research results have to be handled, and even if this committee decides that there is no association and that information gets out, the work has been done and through the freedom of information that will be taken by others and will be used in other ways beyond the control of this group. And I am very concerned about that as I suspect that it is already too late to do anything regardless of any professional body and what they say…My mandate as I sit here in this group is to make sure at the end of the day that 100,000,000 are immunized with DTP, Hepatitis B and if possible Hib, this year, next year and for many years to come, and that will have to be with thimerosal containing vaccines unless a miracle occurs and an alternative is found quickly and is tried and found to be safe.” – Dr. John Clements, World Health Organization, Simpsonwood, GA, June 7, 2000

One can only wonder the harmful effectsnonoxynol 9 could bring.I could find no past flu vaccine that contained this ingredient nor study showing it is safe to inject into humans.

At this point, it must be said. According to the CDC’s vaccine schedule, children now receive 36 vaccines prior to going into kindergarten. This fall season will add 4 additional vaccines to this total for a grand total of 40!? And we’re not even getting warmed up…

POSSIBLE RISKS AND SIDE EFFECTS

By far the most entertaining part of the meeting with Dr. Melamed is when my eyes bugged out on page 6 and 7 of the study. It was explained to me that the side effects I am about to list off are side effects for all vaccines… and that I had nothing to worry about because this vaccine, this vaccine as you recall was made with ‘established technology’. If that is the case, it is the cause for even MORE concern!!!!

Other side effects that have been reported in clinical studies with other influenza vaccines or have been reported by people who received influenza vaccines may include: [VacTRUTH Editor’s Note:Potential Flu Symptoms Highlighted in RED]

Reactions at the site of injection:

• bruising
• itchiness
• rash
• warmth
• lump or irritation at the site where the vaccine was given
• sharp pain in or along nerves or tingling of pins and needles (paresthesia)
• pain limiting movement of the limb where the vaccine was given
• infection
• muscle ache

Other general reactions:

• hot flashes or flushing
• chills or shivering
• dizziness
• generalized weakness
• fainting shortly after vaccination
• nausea
• vomiting
• diarrhea
• loss of appetite
• abdominal pain
• back pain
• lymph node enlargement
• temporary decrease in the number of blood platelets, which may increase the risk of bleeding
• bleeding
• decrease in red blood cells, or anemia, which may make you feel tired.
• high blood pressure (hypertension)
• shortness of breath
• wheezing
• chest tightness
• chest pain
• cough
• sore throat
• runny nose
• “pins and needles” in the skin
• sweating
• skin disorders related to allergic reaction (which can lead to rash and skin loss)
• inflammation of blood vessels (including inflammation of blood vessels that may cause short-term effect on kidneys)
• confusion
• headaches similar to those described as migraine
• seizures associated with fever
• spinal cord or brain inflammation (encephalomyelitis)
• paralysis
• muscle weakness
• infection
• life-threatening and/or debilitating disorders of the nervous system

On IMMUNoE’s website, on page three of  this flier, it states:

“Q: Could the new H1N1 vaccine cause a person to get the flu?

A: Contrary to popular belief, it is not possible to get flu from a flu vaccine. This is true for the seasonal flu vaccine, as well as the investigational(sic) H1N1 vaccine.”

Are the vaccines the same or not the same? Of course, Dr. Melamed at this point tells me about how people with weakened or no immune system can actually get the disease from a vaccine. I asked what measures were being used to understand what the child’s immune response would be (or even if they had an immune response to indicate it was working PRIOR to the vaccine) and Dr. Melamed said, ‘none’. If they don’t measure before and after, how will they know?

“These other general conditions have occurred in people who received influenza vaccines:

• autoimmune disorders (these are disorders in which the body’s tissue are attacked by its own immune system and include liver injury or nerve injury)
• arthritis (joint pain)” (pg 8)

DR ANDREW MOULDEN AND NEUROLOGICAL TESTING

Being a concerned parent one at this point would probably want to know how neurological damage is measured to know if it has occurred in their child. To my surprise, NO NEUROLOGICAL MEASUREMENTS are taken!!! Neurological damage can clearly be seen in past flu vaccines as was the case in the 1975-76 swine flu vaccine.

Dr. Andrew Moulden gives laypersons clinical skills to detect neurological damage occurring after a child or adult is vaccinated. I highly recommend his DVD – Tolerance Lost that is found on hisBrainguard website or reading several articles posted exclusively on VacTRUTH which will give you these skills. They are respectively entitled, “Dr. Andrew Moulden (Interview): What You Were Never Told About Vaccines” and “Vaccinations are causing impaired blood flow (Ischemia), Chronic Illness, Disease and Death for us all“. The second article has photographs showing you precisely what is occurring.

In a separate interview with Dr. Moulden, he succinctly states that if neurological measures are never taken, the industry can say that vaccines are safe.

The only measurements taken will be a brief physical exam, measurement of vital signs and body temperature, blood samples to check for immune response, reviewing diaries with staff, and follow up phone calls. (pg4) Monitoring for safety is occurring for 13 months. How can, then, the vaccines be declared for public use with any certainty of safety in less than 2 months?

“It is also of the understanding that eight investigational (sic) vaccine formulations with different amounts of A/H1N1 antigens and with or without adjuvant will be tested for this study.” (pg 2)

OVERVIEW

Let us recap.
1. The vaccine contains squalene (MF59) which has not been tested for causing cancer.
2. The vaccine contains thimerosal, a known culprit in causing autism and neurological deficits.
3. The vaccine curiously contains nonoxynol-9 used in spermicides.
4. The vaccine will likely cause (and spread) the flu.
5. No neurological testing will be done to ensure the vaccine is safe from harmful neurological side effects.
6. Monitoring for safety will last 13 months, well beyond the flu season.

As to my knowledge, this information is the first of its kind validating the ingredients and the intent to use them on the population. Buyer beware of this vaccine as we are likely to see an onslaught of damaged men, women, and children if there are forced vaccines. The ‘new’ experimental vaccine is certainly unlike any other that we, as Americans, have been exposed to in the past.

Vaccine Trial Paperwork

VacTRUTH Editor’s Note:

1. Check out Jonathan Elinoff’s new website http://vaccinationeducation.com.

2. Dr. Sherri Tenpenny has a great site to educate yourself on the upcoming flu season athttp://pandemicfluonline.com.

3. Dr. Mayer Eisenstein has a free webinar series talking about various topics in vaccinology. Visit his website at http://homefirst.com.

4. Read how pharmaceutical companies plan on superseding parental consent laws to force mass vaccinations here.

5. Visit InTheory.tv for interviews I have done concerning vaccines with Chris Yankowski.

Brian Scott
KIMT 3
September 1, 2009

DES MOINES, IA – Health leaders in Iowa are reassuring people that there are no H1N1 related quarantines being ordered.

Rumors started swirling after a quarantine form was found by someone on the internet.

Polly Carver-Kimm from the state health department says that it’s simply a template that was made months ago.

She says folks shouldn’t expect to see it used anytime soon.

“I can tell you that there are no plans to issue any quarantine or isolation orders this fall for H1N1,” said Carver-Kimm. “We do expect to see lots of cases of that in Iowa, but we also expect to see a large number of seasonal influenza cases.”

The Iowa Department of Public Health recommends folks get flu shots when they become available.

Carver-Kimm also recommends taking simple steps like washing your hands and covering your mouth when coughing.

*Iowa Forced Quarantine Order

Mike Adams
NaturalNews.com
August 28, 2009

The United States of America is devolving into medical fascism and Massachusetts is leading the way with the passage of a new bill, the “Pandemic Response Bill” 2028, reportedly just passed by the MA state Senate and now awaiting approval in the House. This bill suspends virtually all Constitutional rights of Massachusetts citizens and forces anyone “suspected” of being infected to submit to interrogations, “decontaminations” and vaccines.

It’s also sets fines up to $1,000 per day for anyone who refuses to submit to quarantines, vaccinations, decontamination efforts or to follow any other verbal order by virtually any state-licensed law enforcement or medical personnel. You can read the text yourself here:http://www.mass.gov/legis/bills/sen…

Here’s some of the language contained in the bill:

(Violation of 4th Amendment: Illegal search and seizure)

During either type of declared emergency, a local public health authority… may exercise authority… to require the owner or occupier of premises to permit entry into and investigation of the premises; to close, direct, and compel the evacuation of, or to decontaminate or cause to be
decontaminated any building or facility; to destroy any material; to restrict or prohibit assemblages of persons;

(Violation of 14th Amendment; illegal arrest without a warrant)

…an officer authorized to serve criminal process may arrest without a warrant any person whom the officer has probable cause to believe has violated an order given to effectuate the purposes of this subsection and shall use reasonable diligence to enforce such order. [Gunpoint]

(Government price controls)

The attorney general, in consultation with the office of consumer affairs and business regulation, and upon the declaration by the governor that a supply emergency exists, shall take appropriate action to ensure that no person shall sell a product or service that is at a price that unreasonably exceeds the price charged before the emergency.

“Involuntary Transportation” (also known as kidnapping)

Law enforcement authorities, upon order of the commissioner or his agent or at the request of a local public health authority pursuant to such order, shall assist emergency medical technicians or other appropriate medical personnel in the involuntary transportation of such person to the tuberculosis treatment center.

$1,000 / day in fines

Any person who knowingly violates an order, as to which noncompliance
poses a serious danger to public health as determined by the commissioner or the local public health authority, shall be punished by imprisonment for not more than 30 days or a fine of not more than one thousand dollars per day that the violation continues, or both.

Forced vaccinations

Furthermore, when the commissioner or a local public health authority within its jurisdiction determines that either or both of the following measures are necessary to prevent a serious danger to the public health the commissioner or local public health authority may exercise the following authority: (1) to vaccinate or provide precautionary prophylaxis to individuals as protection against communicable disease…

Forced quarantine for those who refuse (illegal imprisonment without charge)

An individual who is unable or unwilling to submit to vaccination or treatment shall not be required to submit to such procedures but may be isolated or quarantined pursuant to section 96 of chapter 111 if his or her refusal poses a serious danger to public health or results in uncertainty whether he or she has been exposed to or is infected with a disease or condition that poses a serious danger to public health, as determined by the commissioner, or a local public health authority operating within its jurisdiction.

Russia Today
August 28, 2009

Herb Newborg
YourSpine
August 5, 2009

The U. S. government has paid pharmaceutical companies $7.9 billion* since 2004 to develop the capacity to mass vaccine the entire U.S. population by 2011. Under the perceived threat of H1N1, these plans have been accelerated to include the use of a non FDA approved chemical adjuvant suspected of causing Gulf War Syndrome, circumventing the FDA approval process for this potentially life threatening chemical.

In 2005, the Department of Health and Human Services (HHS)  published a plan with two specific goals that relate to vaccines. The first goal was to have in place by 2011 domestic production capacity sufficient to supply vaccine to the entire U.S. population within six months of the onset of a pandemic. The second goal was to stockpile enough doses of vaccine to inoculate 20 million people as soon as possible after the onset of a pandemic.

As of September 15, 2008, HHS had yet to determine how best to build and develop the capacity to create the hundreds of millions of doses necessary for such an ambitious undertaking. Three options were identified which could possibly achieve the stated goal by 2011:

Continue to fund and expand funding for the egg-based vaccine antigen production currently utilized in the production of seasonal flu vaccine (viruses are grown in hens’ eggs). Toward this end, HHS has budgeted $600 million to offer capital subsidies to manufacturers to build egg-based production facilities in addition to $176 million already awarded.

Continue to fund and expand funding for cell-based vaccine antigen production (for example, viruses grown in the kidneys of dogs) widely used to manufacture vaccine against polio, chicken pox, measles, mumps, and rubella. To date, HHS has obligated $1.3 billion to promote the development of new cell-based influenza vaccines.

Fund next generation vaccine manufacturing, based on the use of recombinant-DNA technology. Recombinant vaccines are made by splicing antigen producing genes into the DNA of another organism (pigs, monkeys, birds, insects, etc.) The modified organisms then reproduce to provide bulk quantities of antigen. Recombinant techniques are already in use to make vaccines against hepatitis B and human papillomavirus.

All three scenarios had major drawbacks.

Using egg-based vaccine antigen to provide the quantities necessary to vaccinate all 300 million Americans with 2 doses each would require massive infrastructure build up. Despite the $176 million already awarded to manufactures, additional funds would be needed and FDA approvals (not expected until 2011) are necessary in order to even begin to approach the desired number of vaccine doses. It is estimated that the two companies awarded egg-based funding combined could produce only 125 million doses, even after the infrastructure upgrades, and not until 2011.

Using cell-based antigen to provide the quantities necessary to vaccinate all 300 million Americans with 2 doses each would also require massive infrastructure build up. A plant could produce 25 million pandemic-influenza doses at 90 micrograms per dose. It would take about nineteen plants with that capacity to produce 475 million doses. If the cost of construction, bringing the plant online, and obtaining the FDA’s approval averaged $400 million per plant, the total cost of the expanded capacity would be $7.6 billion. If each plant cost $600 million, the total would be $11.4 billion. This capacity would not be available until 2011-2012.

Next generation or recombinant-DNA is not an attractive option, as most recombinant influenza vaccines have not yet advanced past early-stage clinical trials. These vaccines could be 10 years or more away from the market. HHS has yet to fund their development for use against influenza, in part because it has chosen to build on the decades of experience in using cell culture to produce other vaccines. However, HHS plans to award contracts worth $155 million for the development of next-generation vaccines in the near future.

So where does the capacity to mass vaccinate the entire population stand after our $7.9 billion investment?

We currently have a stockpile of 22.5 million doses of the H5N1 antigen for the feared Avian flu pandemic that never materialized. The cost to maintain this stockpile for just two circulating strains of H5N1 is about $2.2 billion annually. Influenza vaccine typically expires after two years; 15 million doses have expired or will expire soon.

In addition, we have stockpiled 268 million doses of what appears to be the wildcard in the whole equation. This is what is known as an adjuvant. An adjuvant is a chemical that can be added to vaccines to reduce the amount of active ingredient (antigen) needed per dose of vaccine by “turbo-charging” the immune system response in the recipient. This could potentially stretch the supply, providing six times as many doses from the same quantity of antigen.

This would solve many, if not all of the issues regarding capacity to mass vaccinate the entire population. Instead of investing in building additional plants and hiring workers to produce antigen, the funds could be used to purchase proprietary, patented chemical adjuvants.

The only problem is: these chemicals are not FDA approved. They have not been FDA safety tested. We have no idea if they are safe and in fact have every reason to suspect that they are not.

Despite this fact, the  U.S. has already purchased at least 312 million doses of two proprietary, patented adjuvants: MF59 from Novartis and ASO3 from GSK. These purchases took place despite the fact that neither chemical has been FDA approved for use in a vaccine. The manufacturers have not yet even obtained FDA approval for Phase I clinical trials in the U.S., the first step toward approval of any new drug, vaccine or adjuvant.

On average, it takes a little over a decade for a drug to move from preclinical development to the marketplace. Before a vaccine enters human testing, the developer conducts laboratory (in vitro) and laboratory animal (in vivo) testing to determine whether the product will be safe enough for researchers to proceed to clinical trials.

The developer must obtain the FDA’s approval to begin clinical trials through the submission of an investigational new drug, or IND, application. Clinical trials typically have three phases. Phase I focuses on the vaccine’s safety and generally involves fewer than 100 human subjects. The purpose of Phase II, which typically involves several hundred subjects, is to expand Phase I safety data and identify whether and at what dose the vaccine elicits a protective immune response. Phase III typically involves thousands of people and is used to document effectiveness and develop additional safety data (notably concerning the incidence and severity of side effects) required for licensing. Clinical trials generally last five to seven years. If all three phases of the clinical development are successful, the developer may submit a biologics license application, or BLA, to the FDA for review. If the FDA approves the application, the developer launches the new vaccine, a process that includes training its sales force and increasing production capabilities to meet the anticipated demand.

It appears that the U.S. is prepared to skip all of the normally required safety and efficacy procedures and allow for the massive testing of this novel adjuvant on at least 25% of the 12,000 Americans serving as paid clinical trial participants in tests of the new H1N1 vaccine, despite documented U.S. government warnings that adjuvanted vaccines can induce more pronounced side effects than ordinary vaccines, a definite downside because vaccines, unlike most other pharmaceuticals, are given to healthy people.

To date, the Food and Drug Administration has never approved an adjuvanted vaccine for influenza. Other adjuvanted vaccines currently licensed for use in the United States—against diphtheria, tetanus, hepatitis A, and hepatitis B—are made with aluminum. But aluminum adjuvants do not reduce the amount of antigen needed by enough to substantially increase the amount of vaccine that would be available during a pandemic.

The FDA has not approved a human vaccine containing a new type of adjuvant in many years, as all other types of adjuvants have thus far produced too many side effects to meet the FDA’s standards.

The reason introducing this chemical without the required safety and efficacy testing is so objectionable is that both of these proprietary adjuvants contain squalene.

Oil-based vaccination adjuvants like squalene have been proved to generate concentrated, unremitting immune responses over long periods of time according to a 2000 article in The American Journal of Pathology.

A 2000 study published in the American Journal of Pathology demonstrated a single injection of the adjuvant squalene into rats triggered “chronic, immune-mediated joint-specific inflammation,” also known as rheumatoid arthritis. The researchers concluded the study raised questions about the role of adjuvants in chronic inflammatory diseases.

What happens when Squalene is injected into humans?

Your immune system recognizes squalene as an oil molecule native to your body. It is found throughout your nervous system and brain. In fact, you can consume squalene in olive oil and not only will your immune system recognize it, you will also reap the benefits of its antioxidant properties.

The difference between “good” and “bad” squalene is the route by which it enters your body. Injection is an abnormal route of entry which incites your immune system to attack all the squalene in your body, not just the vaccine adjuvant.

Your immune system will attempt to destroy the molecule wherever it finds it, including in places where it occurs naturally, and where it is vital to the health of your nervous system, according to award-winning investigative journalist Gary Matsumoto, who explains there is a “close match between the squalene-induced diseases in animals and those observed in humans injected with this oil: rheumatoid arthritis, multiple sclerosis and systemic lupus erythematosus.”

“There are now data in more than two dozen peer-reviewed scientific papers, from ten different laboratories in the US, Europe, Asia and Australia, documenting that squalene-based adjuvants can induce autoimmune diseases in animals…observed in mice, rats, guinea pigs and rabbits. Sweden’s Karolinska Institute has demonstrated that squalene alone can induce the animal version of rheumatoid arthritis. The Polish Academy of Sciences has shown that in animals, squalene alone can produce catastrophic injury to the nervous system and the brain. The University of Florida Medical School has shown that in animals, squalene alone can induce production of antibodies specifically associated with systemic lupus erythematosus,” writes Matsumoto.

We got our first hint at the dangers of these proprietary adjuvants when they were secretly tested on soldiers during the Gulf War.

Gulf War veterans with Gulf War Syndrome (GWS) received anthrax vaccines which contained squalene. MF59 (the Novartis squalene adjuvant) was an unapproved ingredient in experimental anthrax vaccines and has since been linked to the devastating autoimmune diseases suffered by countless Gulf War vets according to data published in the February 2000 and August 2002 issues of Experimental and Molecular Pathology.

The Department of Defense made every attempt to deny that squalene was indeed an added contaminant in the anthrax vaccine administered to Persian Gulf war military personnel – deployed and non-deployed – as well as participants in the more recent Anthrax Vaccine Immunization Program (AVIP).

However, the FDA discovered the presence of squalene in certain lots of AVIP product. A test was developed to detect anti-squalene antibodies in GWS patients, and a clear link was established between the contaminated product and all the GWS sufferers who had been injected with the vaccine containing squalene.

The Pentagon never told Congress about the more than 20,000 hospitalizations involving troops who took the anthrax vaccine from 1998 through 2000, despite repeated promises that such cases would be publicly disclosed. Instead, generals and Defense Department officials claimed that fewer than 100 people were hospitalized or became seriously ill after receiving the shot, according to an investigation by the Daily Press of Newport News.

A study conducted at Tulane Medical School and published in the February 2000 issue of Experimental Molecular Pathology included these stunning statistics:

“ … the substantial majority (95%) of overtly ill deployed GWS patients had antibodies to squalene. All (100%) GWS patients immunized for service in Desert Shield/Desert Storm who did not deploy, but had the same signs and symptoms as those who did deploy, had antibodies to squalene.

In contrast, none (0%) of the deployed Persian Gulf veterans not showing signs and symptoms of GWS have antibodies to squalene. Neither patients with idiopathic autoimmune disease nor healthy controls had detectable serum antibodies to squalene. The majority of symptomatic GWS patients had serum antibodies to squalene.”

According to Dr. Viera Scheibner, Ph.D., a former principle research scientist for the government of Australia:

“… this adjuvant [squalene] contributed to the cascade of reactions called “Gulf War Syndrome,” documented in the soldiers involved in the Gulf War.

The symptoms they developed included arthritis, fibromyalgia, lymphadenopathy, rashes, photosensitive rashes, malar rashes, chronic fatigue, chronic headaches, abnormal body hair loss, non-healing skin lesions, aphthous ulcers, dizziness, weakness, memory loss, seizures, mood changes, neuropsychiatric problems, anti-thyroid effects, anaemia, elevated ESR (erythrocyte sedimentation rate), systemic lupus erythematosus, multiple sclerosis, ALS (amyotrophic lateral sclerosis), Raynaud’s phenomenon, Sjorgren’s syndrome, chronic diarrhoea, night sweats and low-grade fevers.”

Clearly bypassing the FDA requirements for safety testing of these new adjuvants and the vaccines which contain them puts the entire population at risk for serious, possibly life threatening side effects, particularly any of the 12,000 trial paid trial participants (6,000 children) who are unfortunate enough to be randomized into the adjuvant containing groups.

Still, on July 23, 2009, the FDA announced, “Currently, no U.S. licensed vaccine contains the adjuvants MF-59 or ASO3. It is expected that a novel influenza A (H1N1) vaccine manufactured using the same process as U.S. licensed seasonal inactivated influenza vaccine but administered with MF-59 or ASO3 will be authorized for emergency use only.”

And that, “Two of the manufacturers (Novartis and GSK) have proprietary oil-in-water adjuvants (MF-59 and ASO3, respectively) which have been evaluated in a number of clinical studies including studies with influenza vaccines. These manufacturers will include an evaluation of the utility of the adjuvant for dose sparing and enhanced immunogenicity in their clinical studies. While there may be exceptions, in general, studies which include an adjuvanted arm(s) to evaluate dose sparing and enhanced immunogenicity may be conducted concurrently in the adult and pediatric age groups in order to have timely immunogenicity results to guide pediatric dose recommendations.”

The same document indicates that vaccines containing the un-approved adjuvants will be given to 100 children 6 months to 3 years old, 100 children 3 years old to 8 years, 100 individuals 18 to 64 years old and 100 individuals 65 and older in each of the multiple clinical trials. In addition, 700 individuals in each trial will be given non-adjuvanted vaccine.

Since the government has recruited 12,000 paid “volunteers” for the trials, it would be possible that as many as 10 trials could be conducted simultaneously.

Oddly, 60% of the world’s confirmed cases have occurred in people age 18 or younger, yet this age group (between 8 and 18) have been excluded from the clinical trials, with the results for this age group to be extrapolated from the other study data.

Given the fact the U.S. currently owns  268 million doses of the non-approved, non FDA tested adjuvant, the vaccines that contain this novel chemical will likely be found to be completely safe in these industry run trials. Unfortunately, the effects on the soldiers that experienced injury sometimes appeared long after the planned duration of the current trials.

*$5.6 billion in funding occurred in 2006 alone. The $5.6 billion spent for vaccine development in 2006 is 100 times the $515 million the FDA spent in 2006 for all FDA activity related to drug safety and efficacy for the entire drug industry including: pre and post approval testing, approval and regulation of over-the-counter and prescription drugs, biological therapeutics and generic drugs and personal care products such as fluoride toothpaste, antiperspirants, dandruff shampoos and sunscreens, monitor the more than 10,000 drugs on the market to be sure they continue to meet the highest standards, monitor TV, radio, and print drug ads to ensure they are truthful and balanced and provide health professionals and consumers information to use drugs appropriately and safely.

Stephen Lendman
Global Research
August 3, 2009

Alan G. Philips is an attorney with the following credentials:

– he’s one of the few American lawyers whose practice includes vaccine exemption and waiver issues;

– he advises other attorneys seeking help for their own clients on vaccine exemptions;

– he co-founded Citizens for Healthcare Freedom (CHF) as “a grassroots, nonprofit organization supporting an exciting new Consumer Health Freedom Act in North Carolina” where he lives and practices law;

– he “may be the only attorney in the US with a website dedicated to vaccine exemptions” – vaccinerights.com;

– he authored “The Authoritative Guide to Vaccine Legal Exemptions;” and

– he’s written numerous articles and publications on vaccinations and immunizations, including “Dispelling Vaccination Myths: An Introduction to the Contradictions Between Medical Science and Immunization Policy,” published in 1996 and most recently updated in 2007.

Given the possibility of universally mandated untested, experimental, toxic, and extremely dangerous Swine Flu vaccinations this fall, Philips’ work is especially relevant and vital.

In its entirety, it can be accessed at www.vaccinerights.com. A brief account follows below, focusing on 10 myths and truths, which he explains plus some additional information. More than ever, information is vital for protection against vaccines that can cause annoying to life-threatening autoimmune diseases, even the illnesses they’re designed to prevent.

Of special concern is their effect on children. In America and elsewhere, they’re over-immunized enough to destroy their immune systems, leaving them vulnerable to a lifetime of serious health disorders.

No one should voluntarily or otherwise take any vaccine, let alone one as untested and dangerous as for H1N1. But make no mistake. The dominant global media are readying a high intensity fear-mongering campaign to convince the unwary to jeopardize their health and well-being by doing it. Just say NO!!

In America, laws in place empower the Health and Human Services and/or Defense secretaries to declare a national emergency and order mass vaccinations. Legally, individual states can resist, but not likely when enough pressure is applied.

Under the proposed, but not enacted, October 2001 Model State Emergency Health Powers Act (MSEHPA), states are advised on how to exercise extraordinary emergency powers without regard to civil liberties issues. Individual ones have adopted some of its provisions and may add more later given the power of Washington and the media to force them.

The WHO is also empowered under the 2005 International Health Regulations (IHR) to address but not mandate global vaccinations. But it has enough influence to compel nations to go along in case of a “declared” pandemic threat, even without evidence to prove one.

Suspicious H1N1’s Origins

On April 24, AP reported that

“Health officials are investigating a never-before-seen form of the flu that combines pig, bird and human viruses…. (It’s) a growing medical mystery because it’s unclear how (affected people) caught the virus. None (of seven cited had) contact with pigs.” Nor had others reportedly affected in other US cities.

The “intercontinental” mixture included North American Swine Flu, North American Avian Flu, human H1N1 flu, and a fourth H3N2 strain found in Asia and Europe.

Suspicions about a synthetic laboratory-made virus have surfaced. Writing in NewsMax.com, Dr. Russell Blaylock quoted an unnamed viroligist saying: “Where the hell it got all these genes we don’t know.” According to Blalock: “Debate continues over the possibility that swine flu is a genetically engineered virus.”

Dallas County Medical Director Dr. John Carlo voiced concern about the possibility that:

“This strain of swine influenza (may have been) cultured in a laboratory….something that’s not been seen anywhere actually in the United States and the world….”

Recently interviewed on Russia Today TV, investigative journalist Wayne Madsen cited a University of Wisconsin lab conducting joint influenza vaccine research with drug company FluGen. On March 24, Reuters reported that:

“FluGen, Inc., an emerging leader in the development, production and delivery of influenza vaccines and related products, today announced it has secured exclusive rights to a novel, patent-protected vaccine-delivery technology (that) painlessly delivers seasonal and pandemic influenza vaccines.”

Madsen believes “the Swine Flu virus began in a lab,” the objective being profits for vaccine makers with products “that may not actually be safe.” Many noted experts share that view about all vaccines.

NutriMedical founder Dr. William Deagle reported that 6-8% of Swine Flu DNA matches no virus on record. He believes more lethal strains may appear in the fall.

Project Camelot “provide(s) a vehicle for researchers and whistleblowers to get their stories out.” Interviewed on its Whistleblower Radio show, Burk Elder Hale claimed that a senior drug company biochemist (unnamed to protect him) told him:

“….an aerosoled precursor has been put into the air and almost everyone has breathed it into their lungs. (When Swine Flu) vaccines (are) administered in the fall, (they’ll) be activated when (their) constituents come into contact with the aerosoled precursor in the body and will cause a rapid spread of the H1N1 influenza A virus. The biochemist is very upset about the matter….and is a very reliable source that needs our utmost protection.”

Catherine Austin Fitts is a former high-level US government official and Wall Street insider. She’s now the editor of Solari.com and runs Solari, Inc. as an “online media company focusing on ethical investment and preserving family wealth.”

Admitting she’s no expert, she wrote this about Swine Flu on July 22:

“I believe one of the goals of the swine flu vaccine is depopulation. Perhaps it is the goal of a swine flu epidemic as well, whether bio-warfare or hype around a flu season….Lowering immune systems and increasing toxicity levels combined with poor food, water and terrorizing stress will help do the trick….a plague can so frighten and help control people that they will accept the end of their current benefits….without objection. And a plague with proper planning can be highly profitable. Whatever the truth (about) swine flu and related vaccines….it can be used (to) control (a) situation that is quickly shifting out of control.”

“In short, an epidemic can be used to offset the inflation of capital with increasing deflation of the value and income of labor and continual demand destruction. (What’s coming next is the) meaner face of ‘the establishment against the rest of society.’ ”

The possibility of a diabolical depopulation scheme can’t be dismissed. The idea’s been around for decades, including from the 1974 Henry Kissinger project – National Security Study Memorandum 200 (NSSM 200). It was backed by powerful economic interests to cull the world population of useless feeders so corporate giants could exploit world resources unimpeded.

Kissinger’s scheme was to make birth control a prerequisite for US aid. He wanted the annual death rate doubled and for a population decline in the hundreds of millions by 2000. Poor third world women in countries like Brazil were involuntarily sterilized. Millions were harmed then. Perhaps today’s toll from mandatory global Swine Flu vaccinations will be billions.

Yet US laws were passed to prevent it. In 1986, the National Childhood Vaccine Injury Act (NCVIA) required:

– giving parents written information on vaccine benefits and risks so they could decide on what was safe for their children;

– maintaining a permanent record of all vaccines given children, including producer names and lot numbers;

– keeping up to date medical records of all vaccinations given children; and

– recording all serious health problems after vaccinations were administered and notifying the federal Vaccine Adverse Event Reporting System (VAERS) immediately.

At issue is whether federal laws and constitutional and Nuremberg protections will help. Nuremberg requires voluntary consent with full disclosure of known risks and avoidance of experimental treatments if there’s any reason to believe harm may result. The Fifth Amendment protects against abusive government authority in stating that “No person shall….be deprived of life, liberty or property, without due process of law….” The Eighth Amendment prohibits “cruel and unusual punishments.” Harming human health is cruel and abusive. Mandating suspect drugs violates Nuremberg, the US Constitution, and other protective laws. Whether they’ll be enforced is another matter.

Dispelling Vaccination Myths with Truths

Myth No. 1: Vaccines are safe

Under the 1986 National Childhood Vaccine Injury Act, VAERS (Vaccine Adverse Reporting System) was established. Annually, it reports about 11,000 serious vaccine reactions, including up to 200 deaths and many more permanent disabilities.

Far more alarming is the following;

– the FDA estimates that only 1% of serious adverse reactions are reported;

– CDC says it’s 10%;

– medical school students testified before Congress that they’re told not to report these incidents;

– according to the National Vaccine Information Center (NVIC), only one in 40 New York doctors reported adverse vaccine reactions or deaths;

– international studies show vaccines cause up to 10,000 US SIDS (Sudden Infant Death Syndrome) deaths annually, and at least half of them are from vaccines;

– another study determined that 3000 US children die annually from vaccines;

– poor reporting in America suggests that annual adverse vaccine reactions, in fact, number from 100,000 – one million;

– since 1988, the government’s National Vaccine Injury Compensation Program (NVICP) paid families of affected children $1.2 billion in damages;

– as authorized by the 2006 Public Readiness and Emergency Preparedness (PREP) Act, HHS Secretary Sebelius, granted drug companies legal immunity (except for impossible to prove willful misconduct) to proliferate dangerous, untested Swine Flu vaccines globally;

– vaccines are legally mandated in all 50 US states, though legally avoidable in most (under normal circumstances) as explained below;

– in settling vaccine damage suits, drug companies impose gag orders to keep vital information from the public; and

– insurers refuse to cover adverse vaccine reactions because of the high potential liability they’d face.

Truth No. 1

Vaccinations cause high numbers of severe reactions, permanent disabilities, and deaths as well as an enormous personal and public cost. Virtually none of this gets reported.

Myth No. 2: Vaccines are very effective

Medical literature documents significant numbers of vaccine failures for measles, mumps, small pox, pertussis, polio and Hib-causing bacterial meningitis and pneumonia. In 1989, Oman experienced a widespread polio outbreak six months after completing a population-wide immunization program. In Kansas (in 1986), 90% of 1300 reported pertussis cases were “adequately vaccinated,” and 72% of Chicago pertussis incidents in 1993 had been as well.

Truth No. 2

Evidence shows that vaccinations are an unreliable and dangerous way to prevent illness and disease.

Myth No. 3: Low US disease rates are attributable to vaccines

From 1850 – 1940, well before mandatory vaccination programs, the British Association for the Advancement of Science reported a 90% decrease in childhood diseases due to improved sanitation and hygiene practices. By 1945, US medical authorities noted a 95% drop in deaths from the leading childhood infectious diseases (diphtheria, pertussis, scarlet fever and measles), well before mass-immunizations began.

A recent WHO report found that third world disease and mortality rates had no direct correlation with immunization programs, but closely relate to hygiene and diet standards.

Truth No. 3

No evidence links vaccines with infectious disease declines. Proper hygiene and diet practices may be far more effective.

Myth No. 4: Sound immunization theory and practice prove the effectiveness of vaccines

Although vaccines stimulate antibody production, no evidence suggests that alone assures immunity. A 1950 British Medical Council-published study found no relationship between antibody count and disease incidence. Natural immunization involves many bodily organs and systems. Artificially producing antibodies can’t achieve it.

Research also shows how squalene adjuvants harm the human immune system, making it susceptible to numerous illnesses and diseases ranging from very annoying to life threatening. In addition, the “herd immunity” notion of mass-immunizations effectiveness is largely discredited. Just the opposite is true as evidence shows that fully vaccinated populations have experienced epidemics numerous times in the past.

Further, vaccine effectiveness “remains scientifically unproven” because no double blind studies have been conducted to do it. Significantly, recent disease outbreaks have affected more vaccinated children than unvaccinated ones. And the common practice of “one size fits all” is troublesome. It lets tiny new-borns get the same dosage as a five year old. It tolerates dubious quality control practices producing what’s known as “Hot Lots” – ones associated with disproportionately high death and disability rates.

Shockingly, the FDA refuses to act preventatively against them. In fact, individual vaccine lots have almost never been recalled even when associated with severe adverse reactions. Instead, they’re administered under the assumption that all recipients respond the same, regardless of race, ethnicity, genetic makeup, or other characteristics.

A recent New England Journal of Medicine-reported study found that a significant number of Romanian children receiving polio vaccine contracted the disease. Evidence linked antibiotic injections to it. One innoculation raised the polio risk eight-fold; two – nine shots, 27-fold, and 10 or more 182-fold.

New research may reveal other unknown hazards, but public safety won’t be addressed until government health officials act responsibly, report accurately, and adequately protect their populations from vaccines they never should allow.

Truth No. 4

Many supposed vaccine truths have, in fact, been proved false.

Myth No. 5: Childhood diseases are extremely dangerous

False. Even CDC data show a 99.8% pertussis recovery rate during the 1992-94 period. One Cincinnati Children’s Hospital infectious diseases expert said at the time: “The disease was very mild, no one died, and no one went to the intensive care unit.”

Nearly always, childhood infectious diseases “are benign and self-limiting. They usually impart lifelong immunity, whereas vaccine-induced immunization (when achieved) is only temporary.” In fact, it can increase vulnerability later on by postponing better tolerated childhood illnesses until adulthood when death rates (though still low) are far higher.

Most important is that nearly all common infectious diseases are rarely dangerous, and, in fact, can develop strong, healthy adult immune systems when they’re most needed. In addition, few people know that children who didn’t contract measles have a higher incidence of skin diseases, degenerative bone and cartilage ones, and tumors while ovarian cancer is higher among mumps-free adult women. The human immune system benefits from common childhood infectious diseases. Freedom from them may be harmful later on.

Truth No. 5

Childhood disease dangers are greatly exaggerated to scare parents into getting their children vaccinated with unsafe drugs.

Myth No. 6: Polio vaccinations were very successful

False again. In 1955, when the Salk vaccine was introduced, polio was considered the most serious post-war public health problem. A year later, six New England states reported sharp rises ranging from more than double in Vermont to a 642% increase in Massachusetts. Other states also were badly impacted enough for Idaho and Utah to halt immunizations due to increased incidence and death rates.

In his 1962 congressional testimony, Dr. Bernard Greenberg, Biostatistics Department head at the University of North Carolina, reported sharp polio increases from 1957 to 1959 and a Public Health Service whitewash that suppressed it. In 1985, the CDC reported that 87% of US cases between 1973 and 1983 were caused by the vaccine. Later it added that it caused nearly all imported cases, and most of the victims were fully vaccinated.

Further, misdiagnosing, poor reporting, and cover-ups suggest that the actual number of vaccine-associated paralytic polio (VAPP) cases “may be 10 to 100 times higher than that cited by the CDC.”

In 1977, even Jonas Salk admitted that mass inoculations caused most polio cases since 1961.

Truth No. 6

The Salk vaccine proved highly dangerous. Information about it was suppressed, and declines in the disease were well underway when mass-immunizations were begun. In Europe, they occurred in countries that used, then rejected the vaccine proving it was never needed in the first place. Showing also that the same is true for other diseases, including Swine Flu with the WHO and CDC admitting that most cases are mild, unthreatening, and generally pass without treatment, let alone risking dangerous unneeded vaccines.

Myth No. 7: Lack of an initial adverse reaction proves vaccines are safe

Documented long-term health problems include arthritis, chronic headaches, rashes indicative of disease, non-healing skin lesions, seizures, autism, anemia, multiple sclerosis, ALS, cancer, and many others. Ingredients common to all vaccines are at issue. Squalene adjuvants are a biological time bomb that can harm or destroy the human immune system.

Other ingredients are known toxicants and carcinogens, including thimersol (a mercury derivative), aluminum phosphate, formaldehyde, phenoxyethanol, and numerous gastrointestnal toxicants like liver toxicants, cardiovascular and blood toxicants, and reproductive toxicants. “Chemical ranking systems rate many vaccine ingredients among the most hazardous substances” known, even in microscopic doses.

“Millions of children (and adults) are partaking in an enormous crude experiment, and no sincere, organized effort is being made to track the negative side effects or to determine the long-term consequences.”

Dr. Bart Classen’s epidemiological research found vaccines as the cause of 79% of insulin type I diabetes cases in children under 10. The sharp rise in numerous other diseases may also be linked with mass-immunizations. California’s autism rate skyrocketed 1000% in the last 20 years. In the 1990s, MMR vaccine usage in Britain (for measles, mumps and rubella) occurred at the same time autism rose sharply. The January 2000 Journal of Adverse Drug Reactions reported that no adequate testing was done, so the vaccine never should have been licensed.

The Autism Society says: “Autism is a complex developmental disability that typically appears during the first three years of life and is the result of a neurological disorder that affects the normal functioning of the brain….”

According to the CDC and National Vaccine Information Center, one in every 150 US children develop the disease. Tens of millions are affected worldwide, making it more common than pediatric cancer, incurable type 1 (juvenile-onset) diabetes and AIDS combined. In the early 1940s, prior to mass immunizations, autism was so rare that few doctors ever encountered it. Today it’s a global pandemic.

Truth No. 7

Long-term vaccination reactions have been suppressed and ignored in spite of the alarming correlation between their use and the rise of autoimmune and other diseases. Vaccines aren’t for protection. They’re for profit and other nefarious purposes. Avoiding them is essential to protecting human health and well-being.

Myth No. 8: Vaccines are the only available disease prevention option

“Historically, homeopathy has proven many times…more effective than allopathic (conventional) medicine in the treatment and prevention of disease.” During the 1849 US cholera outbreak, homeopathic hospitals documented a 3% death rate compared to 48 – 60% in conventional ones. It’s as true today, and recent epidemiological studies show homeopathic remedies far superior to vaccines in preventing diseases. They’re safe, effective, and toxin and side effect-free, yet most insurers won’t cover them.

Truth No. 8

Alternative treatments and remedies have been safe and effective for generations, yet the medical establishment and governments attack and spurn them.

Myth No. 9: “Vaccinations are legally mandated and unavoidable…”

All states require them. However, laws vary by state, legal exemptions exist, and all states offer one or more of the following:

– all states allow medical exemptions for persons susceptible to adverse reactions; parents can cite this for their children based on family history;

– 48 states offer religious exemptions but may require membership in an established religious organization; “according to federal precedent, personal religious beliefs may be sufficient for a religious exemption regardless of which religious organization you belong to, or whether or not you belong to an organized religion at all;” in addition, the Supreme Court defined religion broadly for legal purposes; and

– 17 states allow philosophical or personal exemptions.

All public and private schools must comply with federal and state vaccination laws and permit legal exemptions.

Truth No. 9

Some vaccines are mandated, but most, perhaps all, US citizens may use legal exemptions to avoid them. In a recent article, however, Phillips states:

“All non-medical exemptions in the US are ultimately provided conditionally. That is, states have the right to require immunization for everyone, legally exempt or not, during an (emergency) outbreak, other than (for) those” with medical exemptions.

Myth No. 10: Governments place public health concerns above all others

Vaccination history shows “documented instances of deceit portraying vaccines as mighty disease conquerors, when in fact vaccines have had little or no discernible impact – or have even delayed or reversed – pre-existing disease declines….Conflicts of interest are the norm in the vaccine industry.” Government agencies like the FDA and CDC are stacked with corporate officials who return to high-paying industry jobs provided they place profit considerations over public health and safety.

In November 2000, concern over this and adverse reactions got the American Association of Physicians and Surgeons (AAPS) to pass a unanimous resolution at its 57th meeting calling for a moratorium on mandatory childhood vaccinations and for doctors to insist on “truly informed consent for (their) use….”

In October 1999, Dr. Bart Classen, founder and CEO of Classen Immunotherapies, told Congress:

“It is clear….that the government’s immunization policies are driven by politics and not by science. I can give numerous examples where employees of the US Public Health Service….appear to be furthering their careers by acting as propaganda officers to support political agendas. In one case….employees of a foreign government, who were funded and working closely with the US Public Health Service, submitted false data to a major medical journal. The true data indicated the vaccine was dangerous; however, the false data” indicated no risk.

In addition, “four letters from the FDA/Public Health Service….clearly reveal(ed) that the anthrax vaccine” approved for US military personnel was done “without the manufacturer performing a single controlled clinical trial.” They’re essential to determine safety and effectiveness. Failure to conduct them proved devastating to the health and well-being of recipients and still does today. Besides, all vaccines are unsafe and some are extremely dangerous.

US military forces receive many or all of the following vaccinations:

– three shots for hepatitis B;

– two for hepatitis A;

– annually for influenza so all military personnel will get Swine Flu shots;

– all military personnel must have documented proof of receiving MMR vaccines for measles, mumps and rubella; those without them them get single doses;

– two varicella (chicken pox) shots;

– smallpox doses every ten years;

– three for polio for adults never vaccinated; those fully vaccinated get a booster shot;

– tetanus-diphtheria and pertussis vaccinations for personnel who haven’t have them in the past 10 years;

– tetanus every 10 years;

– typhoid vaccinations in either oral or injectable forms;

– a multiple dose series for anthrax;

– yellow fever every 10 years in some cases;

– three for rabies and later boosters;

– tuberculosis screening and shots;

– single pneumococcal doses;

– meningococcal vaccinations every five years before deployment to certain regions; and

– three Japanese encephalitis doses in some cases.

Multiple vaccinations for all US military personnel practically assures damage to their immune systems and severe health problems later on.

Truth No. 10

Public health officials approve dangerous vaccines on unsuspecting recipients and profit handsomely for their efforts.

Final Comments

All vaccines are biological weapons that weaken or destroy the human immune system. They often fail to protect against diseases they’re designed to prevent and often cause them. The H1N1 vaccine is experimental, untested, toxic, extremely dangerous, and essential to avoid even if mandated.

In a December 1994 Medical Post article, Dr. Guylaine Lanctot said:

“The medical authorities keep lying. Vaccination has been a disaster on the immune system. It actually causes a lot of illnesses. We are actually changing our genetic code through vaccination….100 years from now we will know that the biggest crime against humanity was vaccines.”

Dr. Viera Scheibner is internationally known as perhaps the leading expert on adverse vaccine reactions. Her analysis concluded that “there is no evidence whatsoever of the ability of vaccines to prevent any diseases. To the contrary, there is a great wealth of evidence that they cause serious side effects.”

Nonetheless, immunization programs proliferate because the profit potential is enormous despite growing numbers of reputable scientific figures citing concerns.

Currently, over 200 new vaccines are being developed “for everything from birth control to (curbing) cocaine addiction.” Around half of them are in clinical trials using human guinea pigs putting their health and safety on the line unwittingly.

New delivery systems are also being developed that include nasal sprays, mosquitoes, and genetically engineered fruits containing vaccine viruses. With every country in the world a potential buyer, health and safety considerations are suppressed for the sake of profits. Unless somehow this madness is stopped, the harm to our children and society will be catastrophic.