Vaccines as Biological Weapons? Live Avian Flu Virus Vaccine Materials placed in Baxter Sent to 18 Countries

Mike Adams
Natural News
Wednesday, March 4, 2009

There'sa popular medical thriller novel in which a global pandemic is intentionally set off by an evil plot designed to reduce the human population. In the book, a nefarious drug company inserts live avian flu viruses into vaccine materials that are distributed to countries around the world to be Injected into patients as "flu shots." Those patients then become carriers for these highly-virulent strains of avian flu which go on to Infect the world population and cause widespread death.

There's only one problem with this story: It's not fiction. Or, at least, the part about live avian flu viruses being inserted into material vaccine is not fiction. It's happening right now.

Deerfield, Illinois-based pharmaceutical company Baxter International Inc.. Has just been caught shipping live avian flu viruses mixed with vaccine material to medical distributors in 18 countries. The "mistake" (if you can call it that, see below ...) was discovered by the National Microbiology Laboratory in Canada. The World Health Organization was alerted and panic spread throughout the community vaccine as health experts asked the obvious question: How could this have happened?

As published on LifeGen.de (http://www.lifegen.de/newsip/showne ...), serious questions are being raised like this:

"Baxter International Inc.. in Austria 'unintentionally contaminated samples with the bird flu virus that were used in laboratories in 3 neighboring countries, raising concern about the potential spread of the Deadly disease. Austria, Germany, Slowenia and the Czech Republic - these are the countries in which labs were hit with dangerous viruses. Not by bioterrorist commands, but by Baxter. In other words: One of the major global pharmaceutical players seems to have lost control on a virus which is considered by many virologists to be one of the components leading some day to a new pandemic. "

Or, put another way, Baxter is acting a whole lot like a biological terrorism organization these days, sending Deadly viral samples around the world. If you mail an envelope full of anthrax to your Senator, you get arrested as a terrorist. So why is Baxter - which mailed samples of a far more Deadly viral strain to labs around the world - getting away with saying, Essentially, "Oops?"

But There'sa bigger question in all this: How could this company have accidentally mixed LIVE avian flu viruses (both H5N1 and H3N2, the human form) material in this vaccine?
Was the viral contamination intentional?

The shocking answer is that this could not have been an accident. Why? Because Baxter International adheres to something called BSL3 (Biosafety Level 3) - a set of laboratory safety protocols that prevent the cross-contamination of materials.

As explained on Wikipedia (http://en.wikipedia.org/wiki/Biosaf ...):

"Laboratory personnel have specific training in handling pathogenic and potentially lethal agents, and are supervised by competent scientists who are experienced in working with these agents. This is considered a neutral or warm zone. All procedures involving the manipulation of infectious materials are conducted within biological safety cabinets or other physical containment devices, or by personnel wearing appropriate personal protective clothing and equipment. The laboratory has special engineering and design features. "


Another Article (Natural News)

Bird Flu Virus Has Mutated into Form That's Deadly to Humans
Thursday, March 06, 2008 by: David Gutierrez, staff writer
Key concepts: Bird flu, Bird flu virus and H5N1

(Natural News) The avian flu has under gone a critical mutation making it easier for the virus to Infect humans, according to a study conducted by researchers at the University of Wisconsin at Madison and published in the journal Plose Pathogens.

"We have identified a specific change that could make bird flu grow in the upper respiratory tract of humans," lead researcher Yoshihiro Kawaoka said.

The H5N1 strain of influenza, also known as "bird flu," has decimated wild and domestic bird populations across the world since it emerged between 1999 and 2002. This highly virulent variety of the flu has been identified as a public health concern because in the past, varieties of influenza have mutated and crossed the species barrier to humans.

Since 2003, 329 humans have been confirmed infected with H5N1, with 201 fatalities. The vast majority of these worked closely with infected birds, such as in the poultry industry.

One of the primary things that keeps bird flu from humans Infect is that the virus has evolved to reproductions most effectively in the bodies of birds, which have an average body temperature of 106 degrees Fahrenheit. Humans, in contrast, have an average body temperature of 98.6 degrees, with temperatures in the nose and throat even lower (91.4 degrees). This fixed temperature difference makes it very difficult for the bird flu virus to survive and grow in the human body.

In the current study, researchers found that a strain of H5N1 has developed a mutation that allows it to thrive in these lower temperatures.

"The viruses that are circulating in Africa and Europe are the ones closest to becoming a human virus," Kawaoka said. But he pointed out that one mutation is not sufficient to turn H5N1 into a major threat to humans.

"Clearly there are more mutations that are needed. We do not know how many mutations are needed for them to become pandemic strains."

"We are rolling the dice with modern poultry farming practices," warned consumer health advocate Mike Adams, author of the book How to Beat the Bird Flu. "By raising chickens in enclosed spaces, treating them with antibiotics, and Denying them access to fresh air, clean water and natural sunlight, we are creating optimal conditions for the breeding of highly infectious diseases that can quickly Mutat into human Pandemics," Adams said . "Given current poultry farming practices, it is only a matter of time before a highly virulent strain crosses the species barrier."
Buzz up!


Original Article : RECENT
DECISION IN CASE Autism proves DR. Carley RIGHT

The following is the ammo by which Big Pharma can be brought to its knees, and the Holocaust or autoimmune diseases and cancer in people and in pets stopped at last. I ask you to circulate it widely. It is time for you to DEMAND that those promoting mercury as the cause of autism respond to what I have written below. If the true intention of these people is to stop this epidemic in our children, then they should let go of their Egos and ADMIT that I have figured out the true cause. Let me first of all encourage you to go to http://www.drcarley.com/the_big_picture.jpg, you will see that I have ALWAYS said it is the BIG PICTURE of assaults to our immune systems (and mercury is there) which combine to cause disease, including autism. But it is the corruption of the immune system caused by the inoculation of viruses which is the root cause of all autoimmune diseases and cancer ... and once this information is in the hands of a critical mass of the people, we will put a stop to the biggest epidemic the world has ever known ... VIDS (Vaccine Induced Diseases). And the individuals who continue to promote mercury as the root cause in the face of this information will be exposed for being intentional disinformers.

Below is a verbatim copy of the U.S. Government concession filed in November of 2007 in a Court of Federal Claims case brought by neurologist Dr. Polarity Jon and his wife claiming that vaccines were the cause of their daughter Hannah's autism. This decision is posted on David Kirby's blog at David Kirby: The Vaccine-Autism Court Document Every American Should Read. David Kirby, author of "Evidence of Harm" is one of the individuals who are distracting the public that autism is "all about the thimerosol. The take home message therefore is that if the mercury is removed, vaccines will be safe. A Bigger LIE HAS NEVER BEEN Told, and my document "Inoculations the True Weapons of Mass Destruction" posted on
[video=google;1803137818942286763]http://video.google.com/videoplay?docid=1803137818942286763[/video] describes the corruption of the immune system caused by the injection of viruses directly into the body, bypassing secretory IgA (an antibody in the upper GI and respiratory Tracts critical for the processing of germ by the immune system for natural immunity to occur).

I was a guest with David Kirby on a radio show which is posted on my website at http://www.drcarley.com/kirby_vs_carley_autism.mp3, on which I confronted him with the fact that autism is actually a non-fatal case of subacute sclerosis panencephalitis caused by Demy Elina tion following vaccine induced encephalitis, and that the name of the condition was changed to autism to hide this self evident fact. I have sent Mr. Kirby copies of the documents on my website, and asked him multiple times to be a guest on one of my internet shows to discuss the "mercury vs Demy Elina based" theories of autism. He will not do so.

What is truly amazing is that he is now mentioning live viruses amongst a Plethora of other potential problems (see # 6 at David Kirby: Government Concedes Vaccine-Autism Case in Federal Court - Now What?). But is he discussing the live viruses bypassing secretory IgA, causing vaccine induced encephalitis and subsequent Demy Elina tion? NO ... he is mentioning live viruses as a cause of mitochondrial damage. So once again, we will now be distracted with this genetic mitochondrial defect ... perhaps develop a test to find the children with this problem before they are vaccinated, when in fact genetic defects can also be caused by vaccines. More confusion and Distraction ... rather than ADMIT that there is no such thing as a safe vaccine ... and the practice should be abandoned altogether, with attention instead placed on strengthening the immune system. Of course, since population reduction is the true agenda of the powers that be, not only will the vaccine push continue ... but viruses are being developed to cause cancer under the Special Virus Cancer Program. The mad scientists have to be stopped ... and this WILL happen once enough people have opened their eyes to the true purpose of vaccines.

I urge all of you to carefully read this decision dated 11/9/07, in which this young girl won her case claiming vaccines caused her autism. Note these important points:

1. 2 days after multiple vaccines (which included the MMR, which has NEVER had mercury), she developed a high fever, high pitched screaming, and was lethargic and irritable. These are symptoms or vaccine induced encephalitis, an inflammation of the brain caused by injection Viruses or LIVE (not from mercury).

2. She also began to arch her back when she Cried (a sign or vaccine induced encephalitis, NOT mercury poisoning).

3. She developed a post-VARI Cella Vaccination RASH (which proves that the vaccination GAVE HER THAT DISEASE). As explained in the quotes from Harrison's Principles of Medicine, 6th edition, p. 943 posted in my response to the CDC on
, "rarely IS PREVENTION OF INFECTIONS PER SE Considered TO BE AN IMPORTANT GOAL OF Vaccination. In fact, asymptomatic infection after vaccination can serve to enhance and prolong the immune response."

4. She was diagnosed with vaccine induced Encephalopathy (degenerative disease of the brain) ... as you will see below, mercury is involved in causing the degenerative disease Alzheimer's, NOT autism).

5. She developed a SEIZURE DISORDERS later on (go to the CDC website at http://www.cdc.gov/vaccines/pubs/vis/downloads/vis-mmr.pdf) and read the vaccine information statement on the MMR vaccine (which has never had mercury), and you will see that one of the side effects is LONG TERM seizures.

6. You will also note that they did genetic testing of the child and found that she has a genetic defect in her cellular energetic (note that vaccines are known to cause GENETIC Mutation due to insertion of plasmid or DNA from the viruses or tissues used to culture them In fact, this is the whole basis on which DNA vaccines are designed). You can read how DNA vaccines cause genetic mutations at Scientific American Digital: Digital archive of all issues from 1993 to present. (you will have to pay $ 7.95 to access this 1999 article from Scientific American, put "genetic vaccines" in the search engine at that site to find the article, and especially see p. 52 of the article). Of course, they are purporting that this is a GOOD thing ... and do not reveal that "regular" vaccines can do the same thing. Vaccines ARE THE SOURCE OF GENETIC Mutation MOST IN PEOPLE AND PETS IN, and once these mutations have occurred, they are then passed on to future generations. Thus, this insane practice has the potential of causing the extinction of humanity itself.

7. You will notice that although the white coat treating Hannah polarity went as far as to do genetic testing in this child, there were NO Anti-myelin OR ANTI-Neuronal FILAMENTS LEVELS DONE, this IS the test that demonstrates Demy Elina tion before it is massive enough to show up on MRI's, and this IS the test that would prove that autism is actually a non-fatal form of subacute sclerosis panencephalitis (which is why this test is almost never done). However, it is a known fact that the measles virus has proteins similar to myelin basic protein, and thus through molecular mimicry, the anti-measles antibody itself can cause Demy Elina tion, and, as quoted from Harrison's above, this production of anti-measles (and possibly anti-myelin and anti-Neuronal filament antibodies formed by injection of tissue culture on which the viruses are grown) is Prolonged because a chronic infection results.

Here is the decision (but please be sure to also read what I have written after it) ...


CHILD [Hannah polarity], a minor,

by her Parents and Natural Guardians [Dr. & Mrs. Jon polarity]






In accordance with RCFC, Appendix B, Vaccine Rule 4 (c), the Secretary of Health and Human Services submit the following response to the petition for compensation filed in this case.


CHILD ( "CHILD") was born on December -, 1998, and weighed eight pounds, in ounces. Petitioners' Exhibit ( "Pet. Ex.") 54 at 13. The pregnancy was complicated by Gestational diabetes. Id. at 13. CHILD received her first Hepatitis B Immunization on December 27, 1998. Pet. Ex. 31 at 2.

From January 26, 1999 through June 28, 1999, CHILD visited the Pediatric Center In Catonsville , Maryland , For well-child examinations and minor complaints, including fever and eczema. Pet. Ex. 31 at 5-10, 19. During this time period, she received the following pediatric vaccination, without incident:

Vaccine Dates administered

Hep B 12/27/98; 1/26/99

IPV 3/12/99, 4/27/99

Hib 3/12/99, 4/27/99, 6/28/99

DTaP 3/12/99, 4/27/99, 6/28/99

Id. at 2.

At seven months of age, CHILD was diagnosed with bilateral otitis media. Pet. Ex. 31 at 20. In the subsequent months between July 1999 and January 2000, she had frequent bolts or otitis media, which doctors treated with multiple antibiotics. Pet. Ex. 2 at 4. On December 3.1999, CHILD was seen by Karl Diehn, MD, at Ear, Nose, and Throat Associates of the Greater Baltimore Medical Center ( "ENT Associates"). Pet. Ex. 31 at 44. Dr. Diehn recommend that CHILD receive PE tubes for her "recurrent otitis media and serious otitis." Id. CHILD received PE tubes in January 2000. Pet. Ex. 24 at 7. Due to CHILD's otitis media, her mother did not allow CHILD to receive the standard 12 and 15 month childhood Immunization. Pet. Ex. 2 at 4.

According to the medical records, CHILD consistently with her developmental milestones during the first eighteen months of her life. The record of an October 5, 1999 visit to the Pediatric Center notes that CHILD was cking mimic sounds, crawling, and sitting. Pet. Ex. 31 at 9. The record of her 12-month pediatric examination notes that she was using the words "Mom" and "Dad," pulling herself up, and cruising. Id. at 10.

At a July 19, 2000 pediatric visit, the pediatrician observed that CHILD "spoke well" and was "alert and active." Pet. Ex. 31 at 11. CHILD's mother reported that CHILD had regular bowel movements and slept through the night. Id. At the July 19, 2000 examination, CHILD received five vaccination - DTaP, Hib, MMR, Varivax, and IPV. Id. at 2, 11.

According to her mother's affidavit, CHILD developed a fever of 102.3 degrees two days after her Immunization and was lethargic, irritable, and Cried for long periods of time. Pet. Ex. 2 at 6. She exhibited intermittent, high-pitched screaming and a decreased response to stimuli. Id. MOM spoke with the pediatrician, who told her that CHILD was having a normal reaction to her Immunization. Id. According to CHILD's mother, this behavior continued over the next for days, and CHILD also began to arch her back when she Cried. Id.

On July 31, 2000, CHILD presented to the Pediatric Center with a 101-102 degree temperature, a diminished appetite, and small red dots on her chest. Pet. Ex. 31 at 28. The nurse practitioner recorded that CHILD was extremely irritable and inconsolable. Id. She was diagnosed with a post-ranged cella vaccination rash. Id. at 29.

Two months later, on September 26, 2000, CHILD returned to the Pediatric Center with a temperature of 102 degrees, Diarrhea, nasal discharge, a reduced appetite, and pulling at her left ear. Id. at 29. Two days later, on September 28, 2000, CHILD was again seen at the Pediatric Center Diarrhea continued her because, she was Congested, and her mother reported that CHILD was crying during Urination. Id. at 32. On November 1, 2000, CHILD received bilateral PE tubes. Id. at 38. On November 13, 2000, a physician at ENT Associates noted that CHILD was "obviously hearing better" and her audiogram was normal. Id. at 38. On November 27, 2000, CHILD was seen at the Pediatric Center with complaints or Diarrhea, vomiting, diminished energy, fever, and a rash on her cheek. Id. at 33. At a follow-up visit, on December 14, 2000, the doctor noted that CHILD had a possible speech delay. Id.

CHILD was evaluated at the Howard County Infants and Toddlers Program, on November 17, 2000, and November 28, 2000, due to concerns about her language development. Pet. Ex. 19 at 2, 7. The assessment team observed deficits in CHILD's communication and social development. Id. at 6. CHILD's mother reported that CHILD had become less responsive to verbal direction in the previous four months and had lost some language skills. Id. At 2.

On December 21, 2000, CHILD returned to ENT Associates because of other obstructions in her right ear and fussiness. Pet. Ex. 31 at 39. Dr. Grace Matesic identified a middle ear effusion and recorded that CHILD was having some balance issues and not progressing with her speech. Id. On December 27, 2000, CHILD visited ENT Associates, where Dr. Grace Matesic observed that CHILD's left PE tube was obstructed with crust. Pet. Ex. 14 at 6. The tube was replaced on January 17, 2001. Id.

Dr. Andrew Zimmerman, a pediatric neurologist, evaluated CHILD at the Kennedy Krieger Children's Hospital Neurology Clinic ( "Krieger Institute") on February 8, 2001. Pet. Ex. 25 at 1. Dr. Zimmerman reported that after CHILD's Immunization of July 19, 2000, an "Encephalopathy progressed to persistent loss of previously acquired language, eye contact, and related business." Id. He noted a disruptions in CHILD's sleep patterns, persistent screaming and arching, the development of pica to foreign objects, and loose Stools. Id. Dr. Zimmerman observed that CHILD watched the fluorescent lights repeatedly during the examination and

would not make eye contact. Id. He diagnosed CHILD with "regressive Encephalopathy with features consistent with an Autistic spectrum disorder, following normal development." Id. At 2. Dr. Zimmerman ordered genetic testing, a magnetic resonance imaging test (MRI), and an electroencephalogram (EEC). Id.

Dr. Zimmerman referred CHILD to the Krieger Institute's Occupational Therapy Clinic and the Center for Autism and Related Disorders ( "CARDS"). Pet. Ex. 25 at 40. She was evaluated at the Occupational Therapy Clinic by Stacey Lakes Stein, OTR / L, on February 23, 2001. Id. The evaluation report summarized that CHILD had deficits in "many areas of sensory processing which decrease [d] her ability to interpret sensory input and influence [d] her motor performance as a result." Id. at 45. CHILD was evaluated by Alice Kau and Kelley Duff, on May 16, 2001, at CARDS. Pet. Ex. 25 at 17. The clinicians concluded that CHILD was developmentally delayed and demonstrated features of Autistic disorder. Id. at 22.

CHILD returned to Dr.. Zimmerman, on May 17, 2001, for a follow-up consultation. Pet. Ex. 25 at 4. An overnight EEC, performed on April 6, 2001, showed no seizure discharges. Id. at 16. An MRI, performed on March 14, 2001, was normal. Pet. Ex. 24 at 16. A G-band test revealed a normal karyotype. Pet. Ex. 25 at 16. Laboratory studies, however, strongly indicated an underlying mitochondrial disorder. Id. at 4.

Dr. Zimmerman referred CHILD for a neuro-genetics consultation to evaluate her abnormal metabolic test results. Pet. Ex. 25 at 8. CHILD with with Dr. Richard Kelley, a specialist in neuro-genetics, on May 22, 2001, at the Krieger Institute. Id. In his assessment, Dr. Kelley Affirmed that CHILD's history and lab results were consistent with "an etiologically unexplained metabolic disorder that appear [ed] to be a common cause of developmental regression." Id. at 7. He continued to note that children with biochemical profiles similar to CHILD's develop normally until sometime between the first and second year of life when their metabolic pattern becomes apparent, at which time they developmentally recourse. Id. Dr. Kelley described this condition as "mitochondrial PPD." Id.

On October 4, 2001, Dr. John Schoffner, at Horizon Molecular Medicine in Norcross , Georgia , CHILD examined to assess whether her clinical manifestations were related to a defect in cellular energetic. Pet. Ex. 16 at 26. After reviewing her history, Dr. Schoffner agreed that the previous metabolic testing was "suggestive of a defect in cellular energetic." Id. Dr. Schoffner recommended a muscle Biopsy, genetic testing, metabolic testing, and cell culture based testing. Id. at 36. A CSF organic acids test, on January 8, 2002, displayed an increased Lactate to pyruvate ratio of 28.1 which can be seen in disorders of mitochondrial oxidative phosphorylation. Id. at 22. Biopsy A muscle test for oxidative phosphorylation disease revealed abnormal results for Type One and Three. Id. at 3. The most prominent findings were scattered atrophic myofibers that were mostly type one oxidative phosphorylation dependent myofibers, mild increase in lipid in selected myofibers, and occasio
nal myofiber with reduced cytochrome c oxidase activity. Id. at 7. After reviewing these laboratory results, Dr. Schoffner diagnosed CHILD with oxidative phosphorylation disease. Id. at 3. In February 2004, a mitochondrial DNA (mtDNA) point mutation analysis revealed a single nucleotide change in the 16S ribosomal RNA gene (T2387C). Id. at 11.

CHILD returned to the Krieger Institute, on July 7, 2004, for a follow-up evaluation with Dr. Zimmerman. Pet. Ex. 57 at 9. He reported CHILD "had done very well" with treatment for a mitochondrial dysfunction. Dr. Zimmerman concluded that CHILD would continue to require services in speech, occupational, physical, and behavioral therapy. Id.

On April 14, 2006, CHILD was brought by ambulance to Athens Regional Hospital and developed a tonic seizure en route. Pet. Ex. 10 at 38. An EEC showed diffuse slowing. Id. At 40. She was diagnosed with having experienced a Prolonged complex partial seizure and transferred to Scottish Rite Hospital . Id. at 39, 44. She experienced no more seizures while at Scottish Rite Hospital and was discharged on the medications Trileptal and Diastal. Id. at 44. A follow-up MRI of the brain, on June 16, 2006, was normal with evidence of a left mastoiditis manifested by distortion of the air cells. Id. at 36. An EEC, performed on August 15, 2006,

showed "Rhythmic epileptiform discharges in the right temporal region and then focal slowing during a witnessed clinical seizure." Id. At 37. CHILD continues to suffer from a seizure disorder.


Medical personnel at the Division of Vaccine Injury Compensation, Department of Health and Human Services (DVIC) have reviewed the facts of this case, as presented by the petition, medical records, and affidavit. After a thorough review, DVIC has concluded that compensation is appropriate in this case.

In sum, DVIC has concluded that the facts of this case meet the statutory criteria for demonstrating that the vaccination CHILD received on July 19, 2000, significantly aggravated an underlying mitochondrial disorder, which predisposed her to deficits in cellular energy metabolism, and manifested as a Encephalopathy with regressive features of autism spectrum disorder. Therefore, respondent recommends that compensation be awarded to petitioners in accordance with 42 USC § 300aa-11 (c) (1) (C) (ii).

DVIC has concluded that CHILD's complex partial seizure disorder, with an onset of almost six years after her July 19, 2000 vaccination is not related to a vaccine-injury.

Respect fully submitted,

Assistant Attorney General

Torts Branch, Civil Division

Deputy Director
Torts Branch, Civil Division

Assistant Director
Torts Branch, Civil Division

s / Linda S. Renzi by s / Lynn E. Ricci Ardella
LINDA S. Renzi
Senior Trial Counsel
Torts Branch, Civil Division
U.S. Department of Justice
PO Box 146
Benjamin Franklin Station
Washington, DC 20044
(202) 616-4133

DATE: November 9, 2007

PS: On Friday, February 22, HHS conceded that this child's complex partial seizure disorder was also caused by her vaccines. Now we the taxpayer will award this family compensation to finance her seizure medication. Surely ALL decent people can agree that is a good thing.

By the way, it''s worth noting that her seizures did not start until six years after the date of vaccination, yet the government acknowledges they were, indeed, linked to the Immunization of July, 2000 - David Kirby

Now I am going to prove to you, BEYOND A SHADOW OF A Doubt, that mercury is a Distraction in the case of autism:

Please go to Alternative Health News Health Products at Health Truth Revealed, click on "inoculations the true weapons of mass destruction", and listen to the interview I did on this very subject on 3/4/08. You will hear Greg Ciola interviewer mention research done at the University or Calgary in Canada regarding mercury's effect on brain neurons, and I thank him for sending me a link to this information. He also mentions an interview he did with John Moore, a researcher in the dangers of mercury who himself was severely injured by mercury poisoning due to multiple amalgam filling. His interview is posted at Alternative Health News Health Products at Health Truth Revealed. You will read on page 16 that Mr.. Moore states that the research done at the University or Calgary shows "the myelin sheathing simply stripped away from the nerve.

Now, go to:

, this is CRITICAL. You will hear and see the effect of mercury on brain neurons demonstrated by the University or Calgary which Mr. Moore refers to. Mercury causes death of the nerve's axon, as the actin and tubulin which make up the neurofibrils are destroyed when mercury binds to the tubulin molecules, causing the neurofibril to collapse, and some neurofibrils form aggregates or tangles. THIS IS THE KEY FEATURE SEEN IN DIAGNOSTIC Alzheimer's Disease, Autism NOT! You will also notice that these neurons in a culture dish do not have myelin on them, in fact, THE myelin Sheath mentioned IS NOT EVEN IN THIS VIDEO. (Side note - when the brains of Alzheimer's patients are studied microscopically, ALUMINUM is found in the middle of these neurofibrillary tangles).

I also encourage you to go to:
, and hear Dr. Boyd Haley discuss autism & thimerosol (be sure to watch all 4 videos in this series). Dr Haley blames thimerosol for Gulf War Syndrome (GWS) as well as autism. I have done many shows on GWS, which has many factors; Gulf War Plague (the infectious component of the syndrome) is due to mycoplasma incognitas which was in the vaccines given to the soldiers. (In fact, this pathogenic mycoplasma has actually been patented by Dr. Shyn Ching Lo of the American Registry of Pathology in Washington , DC , Patent # 5242820). As explained in my paper "Inoculation the True Weapons of Mass Destruction" at
, the injection of vaccines corrupt the immune system and prevent any infective agent from being eliminated from the body. GWS has many other aspects to it, depleted uranium, pyridostigmine pills given to the soldiers, aspartame in their beverages, etc. To blame thimerosol solely for GWS is disinformation in its highest form.

Dr. Haley brings up the work of Dr Andrew Wakefield, whose medical license was Attacked because he demonstrated measles virus in the lymphoid patches in the gouge or Autistic children. DR. BOYD ADMIT HE DID NOT EVEN STUDY THE VIRUS measles. Although Dr Wakefield did not realize that these viruses' significance as a chronic infection is that this leads to a constant production of anti-measles antibody which, through molecular mimicry, then attacks the myelin sheath (causing Demy Elina tion), Dr. Wakefield is being persecuted because his work supports my work, especially since the MMR has NEVER HAD MERCURY. Dr. Haley's work reinforces the notion that if you take mercury out of vaccines, they will be safe. My work there proves is NO SUCH THING as a safe vaccine, due to the corruption of the immune system caused by injection of live viruses.

Dr. Haley also discusses how antibiotics further accelerating the rate damage in these children. The question he does not address is why are the vaccinated children on antibiotics? Answer ... because they have chronic infection caused by inoculation of live bacteria and viruses, as quoted from Harrison's principles of medicine in my response to the CDC (also on my website), "rarely IS PREVENTION OF INFECTIONS PER SE Considered TO BE AN IMPORTANT GOAL OF Vaccination. In fact, asymptomatic infection after vaccination can serve to enhance and prolong the immune response. "(And this immune response is Prolonged Prolonged production of anti-measles antibody which then continue to attack the myelin sheath, causing Demy Elina tion). I also quote from Harrison 's in my CDC response the symptoms or subacute sclerosis panencephalitis (SSPE), and you will see that autism is a non-fatal form of SSPE. The way Dr. Haley gets around the fact that almost every parent reports their child descended into autism following their MMR shot is by saying that the OTHER children received vaccines containing mercury at the same time as they received the MMR.

Dr. Haley also discusses how mercury is more toxic in children with immune disorders. Where did these immune disorders come from? From the corruption of the immune system caused by the inoculation of live viruses. He also discusses that mercury can cause toxicity which affects genetics by decreased methylation of DNA and RNA. However, no mention is made of the genetic mutations caused by injection of plasmid or DNA from the organisms themselves and the tissues that the viruses are cultured on, which is the whole basis of DNA vaccines. That is why this court case focuses on the fact that the child had a genetic defect which caused mitochondrial dysfunction, and states that the child has "a regressive Encephalopathy with features of autism spectrum disorder." Where this mitochondrial defect originated is not discussed ... injection of foreign DNA in prior vaccines in either Hannah or one of her parents, if this defect was inherited. (However, if one of Hannah's parents has this mitochondrial defect, then why don ' t they have autism?)

Lastly, Dr. Haley also states that oral vaccines would be safer, but does not say this is because of the secretory IgA causing proper handling of the germ and its subsequent elimination from the body (as also explained in my paper inoculation), leading to lifelong immunity NATURAL . Of course, if all vaccines were made into oral forms, people may then ask the hard question ... SO WHY IS NOT NATURAL EXPOSURE TO THESE Viruses THE BEST WAY TO GO? This question would stop vaccine production altogether, which would stop the creation of all autoimmune diseases and cancer, which would shut down Big Pharma. THAT IS THE POTENTIAL OF MY INFORMATION, which is why the medical mafia has gone as far as taking my only child, not just my medical license as they tried with Dr. Wakefield in an attempt to shut me down.

I also sent this document to Dr. Paul Offit at offit@email.chop.edu. Dr. Offit has a huge conflict of interest in promoting vaccines, as he developed the rotavirus vaccine which had to be taken off the market as it sent so many children into the operating room with the life threatening condition called intussussception, where the bowel telescopes in on itself . This is what I stated to Dr. Offit: "I am anxious to hear you present your evidence that autism is not a non fatal form of subacute sclerosis panencephalitis, since the only evidence you presented in your recent book vaccinated praising Maurice Hilleman was that SSPE is always fatal." No response from Dr. Offit, who has also publicly made the insane statement that "children can handle 10,000 vaccines at one time."

If you want to learn how the post-encephalitic syndrome caused by vaccines causes changes in the brain that lead to violence and criminal behavior, please go to
and order the highly referenced book Vaccination, Social Violence and Criminality by Harris Coulter, PhD. Do you now see how vaccines contribute to the ever increasing violence being seen in our young people, not to mention how many children are subsequently put on psychiatric drugs after sustaining neurological vaccine damage leading to ADD, ADHD, etc. As Big Pharma has just started to ADMIT, these drugs have a side effect of homicide and suicide.

Are you beginning to realize how important it is to stop this insane practice of inoculating our children with disease, and instead give them natural supplements to boost their natural immunity?

Can you handle knowing the fact that all this is being done to the children ON PURPOSE? Then go to Republic Broadcasting Network 8 253Fcmd% 253Darchives.getyear% 2526ProgramID% 253D36% 26year% 3D8% 26backURL% 3Dindex . 253Fcmd php%% 253Darchives
and listen to the 2nd hour of my interview with Dr on 3/5/08. True Ott, where he discusses how the history of MediSIN goes back to the 1600's as detailed in the Magnum Opus by Jesuit Del Rio, with the creation or amulet by sacrifice animals and mixing their blood with mercuriale compounds TO CAST A GAMES AND CONTROL THE MIND OF THE POPULATION (Dr Ott discusses this starting at 13 minutes of the 2nd hour of our interview). He explains how the origins of the word "pharmaceutical" in Latin is "pharmakia", which translates to "SORCERY". Yes, folks ... you have now entered the rabbit hole ... because nothing has changed since the 1600's.

I have been trying for 10 years to stop the Holocaust vaccination on people and pets. I have proven, with the quoted studies and works of the "mercury causes autism" disinformers themselves, that it is NOT MERCURY WHICH causes autism. I leave it up to you to forward this e-mail to all the individuals and groups which promote mercury as the cause of autism, so you will see for yourselves who is intentionally misleading you, vs. who was misguided. You will know which is the case by whether or not they respond. Silence is consent that I am right, and if they do not join with me to stop this holocaust altogether, you must then ask yourself WHY. IT IS TIME FOR THOSE WITH HONOR Intentions ABLE TO JOIN WITH ME TO STOP THIS OR VIDS Epidemic. I have already sent this document to Dr. Boyd Haley (behaley@uky.edu) and David Kirby (brook200@hotmail.com), please do so yourselves.

Let's roll ....

Dr Carley