Updates from Dr. Carley: Re: the Federal Case admitting that autism was caused by vaccines

[Guest guest]

Awesome. God Bless you Dr. Carley!

, BS.HT

Board Certified Holistic Practitioner

www.SignificantHealing.com

www.ZeoliteExpert.com

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>

> Dear List;

>

> You have not received any updates from me in some time, as the

program which

> allows me to do so was sabotaged, and it took my webmaster all this

time to

> fix it. I thank her for not giving up until she was successful, as

this is

> one of the most important documents I have ever written. She is

the best!

>

> The following is the ammo by which Big Pharma can be brought to its

knees.

> 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 encourage of all 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 US Government concession filed last

November

> in a Court of Federal Claims case brought by a family claiming that

mercury

> containing vaccines were the cause of the child's autism that is

posted on

> Kirby's blog at

> http://www.huffingtonpost.com/david-kirby/the-vaccineautism-court-

_b_88558.h

> tml. Kirby, author of " Evidence of Harm " , is one of the

individuals

> who is distracting the public that it is " all about the

thimerosol " . The

> take home message therefore is that if the mercury were removed,

vaccines

> would be safe. A BIGGER LIE HAS NEVER BEEN TOLD; and my document

> " Inoculations the True Weapons of Mass Destruction " posted on

> www.drcarley.com 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 the germ by the immune system for natural immunity to occur).

>

> I was a guest with 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

> sclerosing panencephalitis caused by demyelination 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 demyelination " 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

> http://www.huffingtonpost.com/david-kirby/government-concedes-

vacci_b_88323.

> html)....but is he discussing the live viruses bypassing secretory

IgA,

> causing vaccine induced encephalitis and subsequent demyelination?

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

admitting that

> there is no such thing as a safe vaccine...and the practice should

be

> abandoned altogether, and attention 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 a

> re being developed to cause disease and cancer. The mad scientists

have to

> be stopped...and this WILL happen once enough people have opened

their eyes.

>

> 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 of VACCINE INDUCED

> ENCEPHALITIS, an inflammation of the brain caused by injection of

LIVE

> VIRUSES (not from mercury).

>

> 2. She also began to arch her back when she cried (a sign of

vaccine induced

> encephalitis, NOT mercury poisoning).

>

> 3. She developed a POST-VARICELLA VACCINATION RASH (which proves

that the

> vaccination GAVE HER THAT DISEASE).

>

> 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 DISORDER later on (go to the CDC

website and

> look for 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 energetics (Note that

vaccines

> are known to cause GENETIC MUTATION due to insertion of plasmids of

DNA from

> the viruses or tissues used to culture them; in fact, this is the

whole

> basis on which DNA vaccines are designed).

>

> 7. You will notice that although the white coat in this case went

as far as

> to do genetic testing in this child, there were NO ANTI MYELIN OR

ANTI

> NEURONAL FILAMENT LEVELS DONE; this IS the test that demonstrates

> demyelination before it is massive enough to show up on MRI's; and

this IS

> the test that proves that autism is actually a non-fatal form of

subacute

> sclerosing panencephalitis (which is why this test is almost never

done).

>

> Here is the decision (but please be sure to also read what I have

written

> after it)...

>

> IN THE UNITED STATES COURT OF FEDERAL CLAIMS

> OFFICE OF SPECIAL MASTERS

>

>

> CHILD, a minor,

>

> by her Parents and Natural Guardians,

>

> Petitioners,

>

> v.

>

> SECRETARY OF HEALTH AND HUMAN SERVICES,

>

> Respondent.

>

> RESPONDENT'S RULE 4© REPORT

>

> In accordance with RCFC, Appendix B, Vaccine Rule 4©, the

Secretary of

> Health and Human Services submits the following response to the

petition for

> compensation filed in this case.

>

> FACTS

>

> CHILD ( " CHILD " ) was born on December --, 1998, and weighed

eight pounds,

> ten 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, land, 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 vaccinations,

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 bouts of otitis media, which doctors treated

with

> multiple antibiotics. Pet. Ex. 2 at 4. On December 3,1999, CHILD

was seen by

> Karl Diehn, M.D., 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 immunizations. Pet. Ex. 2 at

4.

>

> According to the medical records, CHILD consistently met 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 mimicking 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

vaccinations -

> 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 immunizations 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 immunizations. Id. According to CHILD's mother, this behavior

> continued over the next ten 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-

varicella

> 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

because her

> diarrhea continued, 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 of 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 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 an

> obstruction 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. 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 immunizations of July 19, 2000, an " encephalopathy

progressed to

> persistent loss of previously acquired language, eye contact, and

> relatedness. " Id. He noted a disruption 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 ( " EEG " ). 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 Merenstein, 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 EEG, 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 neurogenetics consultation to

> evaluate her abnormal metabolic test results. Pet. Ex. 25 at 8.

CHILD met

> with Dr. Kelley, a specialist in neurogenetics, 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 regress. Id.

Dr. Kelley

> described this condition as " mitochondrial PPD. " Id.

>

> On October 4, 2001, Dr. Schoffner, at Horizon Molecular

Medicine in

> Norcross, Georgia, examined CHILD to assess whether her clinical

> manifestations were related to a defect in cellular energetics.

Pet. Ex. 16

> at 26. After reviewing her history, Dr. Schoffner agreed that the

previous

> metabolic testing was " suggestive of a defect in cellular

energetics. " 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. A muscle biopsy 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 EEG

> showed diffuse slowing. Id. At 40. She was diagnosed with having

experienced

> a prolonged complex partial seizure and transferred to ish Rite

> Hospital. Id. at 39, 44. She experienced no more seizures while at

ish

> 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 EEG, 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.

>

> ANALYSIS

>

> 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

affidavits.

> 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 vaccinations 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 regressive encephalopathy with features of

autism

> spectrum disorder. Therefore, respondent recommends that

compensation be

> awarded to petitioners in accordance with 42 U.S.C. § 300aa-11©(1)

©(ii).

>

> DVIC has concluded that CHILD's complex partial seizure

disorder, with

> an onset of almost six years after her July 19, 2000 vaccinations,

is not

> related to a vaccine-injury.

>

> Respectfully submitted,

>

> PETER D. KEISLER

> Assistant Attorney General

>

> TIMOTHY P. GARREN

> Director

> Torts Branch, Civil Division

>

> MARK W. ROGERS

> Deputy Director

> Torts Branch, Civil Division

>

> VINCENT J. MATANOSKI

> Assistant Director

> Torts Branch, Civil Division

>

> s/ S. Renzi by s/ Lynn E. Ricciardella

> LINDA S. RENZI

> Senior Trial Counsel

> Torts Branch, Civil Division

> U.S. Department of Justice

> P.O. Box 146

> lin Station

> Washington, D.C. 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

taxpayers 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 begin

until six

> years after the date of vaccination, yet the government

acknowledges they

> were, indeed, linked to the immunizations of July, 2000, -

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 http://healthtruthrevealed.com/audio-interviews.php,

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

> mention research done at the University of Calgary 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 ,

a

> researcher in the dangers of mercury who himself was severely

injured by

> mercury poisoning due to multiple amalgam fillings. His interview

is posted

> at http://healthtruthrevealed.com/full-page.php?id=39 & & page=news.

You will

> read on page 16 that Mr. states that the research done at the

> University of 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 of Calgary which Mr. refers to. Mercury

causes DEATH

> of the nerve's axon, as the actin & 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 DIAGNOSTIC FEATURE SEEN IN ALZHEIMER'S DISEASE; NOT

AUTISM!

> You will also notice that these neurons in a culture dish do not

have myelin

> on then; in fact, THE MYELIN SHEATH IS NOT EVEN MENTIONED 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

> http://video.google.com/videoplay?docid=1803137818942286763, 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. As

explained in

> my document " Inoculation the true weapons of mass destruction " at

> www.drcarley.com, the injection of vaccines corrupts the immune

system and

> prevents 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 Wakefield, whose medical

license

> was attacked because he demonstrated measles virus in the lymphoid

patches

> in the guts of autistic children. DR. BOYD ADMITS HE DID NOT EVEN

STUDY THE

> MEASLES VIRUS. 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

> attackes the myelin sheath (causing demyelination), he was attacked

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 proves there 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 accelerate the

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 viruses; as quoted from on's

principles

> of medicine in my response to the CDC (also on my website), " RARELY

IS

> PREVENTION OF INFECTION 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 prolonged

immune

> response IS prolonged production of anti-measles antibody which then

> continue to attack the myelin sheath, causing demyelination). As I

also

> quote from on's in my CDC response the symptoms of subacute

sclerosing

> panencephalitis (SSPE), 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 fo

> llowing their MMR shot is by saying that the children received OTHER

> 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 & RNA. However, no mention is made of

the

> genetic mutations caused by injection of plasmids of 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. Where this defect originated is not

discussed...injection of

> foreign DNA in prior vaccines (You will note in the court decision

that the

> parents were not tested for this defect, as that would have proven

that this

> is NOT an inherited genetic defect, but rather a mutation that

occurred in

> this child de novo).

>

> Lastly, Dr. also states that oral vaccines would be safer, but does

not say

> this is because of the secretory IgA causing proper handling of the

antigen

> (as also explained in my inoculation paper), leading to life long

NATURAL

> immunity. Of course, if all vaccines were made into oral forms,

people may

> then ask the hard question...SO WHY ISN'T 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.

>

> Can you handle knowing the fact that all this is being done to the

children

> ON PURPOSE? Then go to

> http://www.republicbroadcasting.org/index.php?

cmd=archives.month & ProgramID=3

> 6 & year=8 & month=3 & backURL=index.php%253Fcmd%253Darchives.getyear%

2526ProgramI

> D%253D36%26year%3D8%26backURL%3Dindex.php%253Fcmd%253Darchives

> and listen to the 2nd hour of my interview on 3/5/08 with Dr. True

Ott,

> where he discusses how the history of MediSIN goes back to the

1600's as

> detailed in the Magnum Opus, with the creation of amulets by

sacrificing

> animals and mixing their blood with mercurial compounds TO CAST A

SPELL AND

> CONTROL THE MINDS OF THE POPULATIONS (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 vaccination holocaust

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 HONORABLE INTENTIONS TO JOIN WITH ME TO STOP THIS EPIDEMIC OF

VIDS. I

> have already sent this to Dr. Boyd Haley (behaley@...) and

Kirby

> (brook200@...); please do so yourselves.

>

> Let's roll....

>

> Namaste,

> Dr Carley

>

> --

> Dr. Carley

> http://www.drcarley.com

>

> *** Dr. Carley's information is not intended to diagnose, treat or

cure any

> diseases. Rather, it is for educational purposes only. ***

>

>

> No virus found in this outgoing message.

> Checked by AVG Free Edition.

> Version: 7.5.516 / Virus Database: 269.21.4/1312 - Release Date:

03/04/2008

> 21:46

>

[Guest guest]

Awesome. God Bless you Dr. Carley!

, BS.HT

Board Certified Holistic Practitioner

www.SignificantHealing.com

www.ZeoliteExpert.com

>

>

>

>

>

>

>

>

>

> Dear List;

>

> You have not received any updates from me in some time, as the

program which

> allows me to do so was sabotaged, and it took my webmaster all this

time to

> fix it. I thank her for not giving up until she was successful, as

this is

> one of the most important documents I have ever written. She is

the best!

>

> The following is the ammo by which Big Pharma can be brought to its

knees.

> 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 encourage of all 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 US Government concession filed last

November

> in a Court of Federal Claims case brought by a family claiming that

mercury

> containing vaccines were the cause of the child's autism that is

posted on

> Kirby's blog at

> http://www.huffingtonpost.com/david-kirby/the-vaccineautism-court-

_b_88558.h

> tml. Kirby, author of " Evidence of Harm " , is one of the

individuals

> who is distracting the public that it is " all about the

thimerosol " . The

> take home message therefore is that if the mercury were removed,

vaccines

> would be safe. A BIGGER LIE HAS NEVER BEEN TOLD; and my document

> " Inoculations the True Weapons of Mass Destruction " posted on

> www.drcarley.com 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 the germ by the immune system for natural immunity to occur).

>

> I was a guest with 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

> sclerosing panencephalitis caused by demyelination 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 demyelination " 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

> http://www.huffingtonpost.com/david-kirby/government-concedes-

vacci_b_88323.

> html)....but is he discussing the live viruses bypassing secretory

IgA,

> causing vaccine induced encephalitis and subsequent demyelination?

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

admitting that

> there is no such thing as a safe vaccine...and the practice should

be

> abandoned altogether, and attention 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 a

> re being developed to cause disease and cancer. The mad scientists

have to

> be stopped...and this WILL happen once enough people have opened

their eyes.

>

> 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 of VACCINE INDUCED

> ENCEPHALITIS, an inflammation of the brain caused by injection of

LIVE

> VIRUSES (not from mercury).

>

> 2. She also began to arch her back when she cried (a sign of

vaccine induced

> encephalitis, NOT mercury poisoning).

>

> 3. She developed a POST-VARICELLA VACCINATION RASH (which proves

that the

> vaccination GAVE HER THAT DISEASE).

>

> 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 DISORDER later on (go to the CDC

website and

> look for 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 energetics (Note that

vaccines

> are known to cause GENETIC MUTATION due to insertion of plasmids of

DNA from

> the viruses or tissues used to culture them; in fact, this is the

whole

> basis on which DNA vaccines are designed).

>

> 7. You will notice that although the white coat in this case went

as far as

> to do genetic testing in this child, there were NO ANTI MYELIN OR

ANTI

> NEURONAL FILAMENT LEVELS DONE; this IS the test that demonstrates

> demyelination before it is massive enough to show up on MRI's; and

this IS

> the test that proves that autism is actually a non-fatal form of

subacute

> sclerosing panencephalitis (which is why this test is almost never

done).

>

> Here is the decision (but please be sure to also read what I have

written

> after it)...

>

> IN THE UNITED STATES COURT OF FEDERAL CLAIMS

> OFFICE OF SPECIAL MASTERS

>

>

> CHILD, a minor,

>

> by her Parents and Natural Guardians,

>

> Petitioners,

>

> v.

>

> SECRETARY OF HEALTH AND HUMAN SERVICES,

>

> Respondent.

>

> RESPONDENT'S RULE 4© REPORT

>

> In accordance with RCFC, Appendix B, Vaccine Rule 4©, the

Secretary of

> Health and Human Services submits the following response to the

petition for

> compensation filed in this case.

>

> FACTS

>

> CHILD ( " CHILD " ) was born on December --, 1998, and weighed

eight pounds,

> ten 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, land, 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 vaccinations,

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 bouts of otitis media, which doctors treated

with

> multiple antibiotics. Pet. Ex. 2 at 4. On December 3,1999, CHILD

was seen by

> Karl Diehn, M.D., 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 immunizations. Pet. Ex. 2 at

4.

>

> According to the medical records, CHILD consistently met 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 mimicking 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

vaccinations -

> 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 immunizations 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 immunizations. Id. According to CHILD's mother, this behavior

> continued over the next ten 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-

varicella

> 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

because her

> diarrhea continued, 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 of 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 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 an

> obstruction 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. 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 immunizations of July 19, 2000, an " encephalopathy

progressed to

> persistent loss of previously acquired language, eye contact, and

> relatedness. " Id. He noted a disruption 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 ( " EEG " ). 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 Merenstein, 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 EEG, 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 neurogenetics consultation to

> evaluate her abnormal metabolic test results. Pet. Ex. 25 at 8.

CHILD met

> with Dr. Kelley, a specialist in neurogenetics, 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 regress. Id.

Dr. Kelley

> described this condition as " mitochondrial PPD. " Id.

>

> On October 4, 2001, Dr. Schoffner, at Horizon Molecular

Medicine in

> Norcross, Georgia, examined CHILD to assess whether her clinical

> manifestations were related to a defect in cellular energetics.

Pet. Ex. 16

> at 26. After reviewing her history, Dr. Schoffner agreed that the

previous

> metabolic testing was " suggestive of a defect in cellular

energetics. " 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. A muscle biopsy 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 EEG

> showed diffuse slowing. Id. At 40. She was diagnosed with having

experienced

> a prolonged complex partial seizure and transferred to ish Rite

> Hospital. Id. at 39, 44. She experienced no more seizures while at

ish

> 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 EEG, 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.

>

> ANALYSIS

>

> 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

affidavits.

> 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 vaccinations 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 regressive encephalopathy with features of

autism

> spectrum disorder. Therefore, respondent recommends that

compensation be

> awarded to petitioners in accordance with 42 U.S.C. § 300aa-11©(1)

©(ii).

>

> DVIC has concluded that CHILD's complex partial seizure

disorder, with

> an onset of almost six years after her July 19, 2000 vaccinations,

is not

> related to a vaccine-injury.

>

> Respectfully submitted,

>

> PETER D. KEISLER

> Assistant Attorney General

>

> TIMOTHY P. GARREN

> Director

> Torts Branch, Civil Division

>

> MARK W. ROGERS

> Deputy Director

> Torts Branch, Civil Division

>

> VINCENT J. MATANOSKI

> Assistant Director

> Torts Branch, Civil Division

>

> s/ S. Renzi by s/ Lynn E. Ricciardella

> LINDA S. RENZI

> Senior Trial Counsel

> Torts Branch, Civil Division

> U.S. Department of Justice

> P.O. Box 146

> lin Station

> Washington, D.C. 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

taxpayers 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 begin

until six

> years after the date of vaccination, yet the government

acknowledges they

> were, indeed, linked to the immunizations of July, 2000, -

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 http://healthtruthrevealed.com/audio-interviews.php,

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

> mention research done at the University of Calgary 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 ,

a

> researcher in the dangers of mercury who himself was severely

injured by

> mercury poisoning due to multiple amalgam fillings. His interview

is posted

> at http://healthtruthrevealed.com/full-page.php?id=39 & & page=news.

You will

> read on page 16 that Mr. states that the research done at the

> University of 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 of Calgary which Mr. refers to. Mercury

causes DEATH

> of the nerve's axon, as the actin & 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 DIAGNOSTIC FEATURE SEEN IN ALZHEIMER'S DISEASE; NOT

AUTISM!

> You will also notice that these neurons in a culture dish do not

have myelin

> on then; in fact, THE MYELIN SHEATH IS NOT EVEN MENTIONED 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

> http://video.google.com/videoplay?docid=1803137818942286763, 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. As

explained in

> my document " Inoculation the true weapons of mass destruction " at

> www.drcarley.com, the injection of vaccines corrupts the immune

system and

> prevents 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 Wakefield, whose medical

license

> was attacked because he demonstrated measles virus in the lymphoid

patches

> in the guts of autistic children. DR. BOYD ADMITS HE DID NOT EVEN

STUDY THE

> MEASLES VIRUS. 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

> attackes the myelin sheath (causing demyelination), he was attacked

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 proves there 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 accelerate the

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 viruses; as quoted from on's

principles

> of medicine in my response to the CDC (also on my website), " RARELY

IS

> PREVENTION OF INFECTION 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 prolonged

immune

> response IS prolonged production of anti-measles antibody which then

> continue to attack the myelin sheath, causing demyelination). As I

also

> quote from on's in my CDC response the symptoms of subacute

sclerosing

> panencephalitis (SSPE), 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 fo

> llowing their MMR shot is by saying that the children received OTHER

> 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 & RNA. However, no mention is made of

the

> genetic mutations caused by injection of plasmids of 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. Where this defect originated is not

discussed...injection of

> foreign DNA in prior vaccines (You will note in the court decision

that the

> parents were not tested for this defect, as that would have proven

that this

> is NOT an inherited genetic defect, but rather a mutation that

occurred in

> this child de novo).

>

> Lastly, Dr. also states that oral vaccines would be safer, but does

not say

> this is because of the secretory IgA causing proper handling of the

antigen

> (as also explained in my inoculation paper), leading to life long

NATURAL

> immunity. Of course, if all vaccines were made into oral forms,

people may

> then ask the hard question...SO WHY ISN'T 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.

>

> Can you handle knowing the fact that all this is being done to the

children

> ON PURPOSE? Then go to

> http://www.republicbroadcasting.org/index.php?

cmd=archives.month & ProgramID=3

> 6 & year=8 & month=3 & backURL=index.php%253Fcmd%253Darchives.getyear%

2526ProgramI

> D%253D36%26year%3D8%26backURL%3Dindex.php%253Fcmd%253Darchives

> and listen to the 2nd hour of my interview on 3/5/08 with Dr. True

Ott,

> where he discusses how the history of MediSIN goes back to the

1600's as

> detailed in the Magnum Opus, with the creation of amulets by

sacrificing

> animals and mixing their blood with mercurial compounds TO CAST A

SPELL AND

> CONTROL THE MINDS OF THE POPULATIONS (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 vaccination holocaust

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 HONORABLE INTENTIONS TO JOIN WITH ME TO STOP THIS EPIDEMIC OF

VIDS. I

> have already sent this to Dr. Boyd Haley (behaley@...) and

Kirby

> (brook200@...); please do so yourselves.

>

> Let's roll....

>

> Namaste,

> Dr Carley

>

> --

> Dr. Carley

> http://www.drcarley.com

>

> *** Dr. Carley's information is not intended to diagnose, treat or

cure any

> diseases. Rather, it is for educational purposes only. ***

>

>

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03/04/2008

> 21:46

>