LONG NEWS/INFO POST! Dr Carley critiques the Fed Ct decision admi...

[Guest guest]

PERMISSION BY DR. CARLEY TO REPOST FREELY:

Dr Carley critiques the Fed Ct decision admitting vaccine caused autism

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

and the holocaust of 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 encourage of all you to go to

_http://www.drcarleyhttp://wwhttp://www.dhtt_

(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 in November

of 2007 in a Court of Federal Claims case brought by neurologist Dr. Jon

Poling and his wife claiming that vaccines were the cause of their daughter

Hannah's autism. This decision is posted on Kirby's blog at

_http://www.huffingthttp://www.http://www.hhttp://www.huffihttp://wwhttp://www.h\

_

(http://www.huffingtonpost.com/david-kirby/the-vaccineautism-court-_b_88558.html\

) .

Kirby, author of " Evidence of Harm " , is one of the individuals who is

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 _www.drcarley.www_

(http://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 germs 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.drcarleyhttp://www.http://wwwhttp://www_

(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.huffingthttp://www.http://www.hhttp://www.http://wwhttp://www.hufhtt\

p_

(http://www.huffingtonpost.com/david-kirby/government-concedes-vacci_b_88323.htm\

l) ). 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. More

confusion and distraction.<WBR>..rather than admitting that there is no such

thing as a safe vaccine...and the practice should be abandoned altogether,

with attention instead pla 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 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). As explained in the quotes from

on's Principles of Medicine, 6th edition, p. 943 posted in my response to

the

CDC on _www.drcarley.www_ (http://www.drcarley.com/) , " 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. "

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 at

_http://www.cdc.http://www.cdhttp://wwhttp://wwwhttp://www._

(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 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). You can read how DNA vaccines cause

genetic mutations at

_http://sciamdigitalhttp://sciahttp://sciamdihttp://sciamdigihttp://scia_

(http://sciamdigital.com/index.cfm?fa=Search.ViewSearchForItemResultList) (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 MOST GENETIC

MUTATIONS IN PEOPLE AND IN PETS; 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 Poling 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 would prove that autism is actually a non-fatal form of subacute

sclerosing panencephalitis (which is why this test is almost never done).

However,

it is a known fact that the measles virus has similar proteins to myelin

basic protein, and thus through molecular mimicry, the anti-measles antibody

itself can cause demyelination; and, as quoted from on'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)...

IN THE UNITED STATES COURT OF FEDERAL CLAIMS

OFFICE OF SPECIAL MASTERS

CHILD [Hannah Poling], a minor,

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

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 " ) 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

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 i

rritable 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. reported

that after CHILD's immunizations of July 19, 2000, an " encephalopathy

progressed

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

relatedness.<WBR> " Id. He noted a disruption in CHILD's sleep patterns,

persistent

screaming an

would not make eye contact. Id. He diagnosed CHILD with " regressive

encephalopathy with features consistent with an autistic spectrum disorder,

following

normal development. would not make eye contact. Id. He diagnosed CHILD with

" regressive encephalopathy with features consistent with an a would not make

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 accord

ance with 42 U.S.C. § 300aa-11©( In sum

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://healthtruthrhttp://healthttp://healthtruhttp_

(http://healthtruthrevealed.com/audio-interviews.php) , click on " inoculations

the

true weapons of mass destruction " , click on " inoculations the true weapons of

mass destruction " <WBR> You will hear interviewer Greg Ciola mention research

done at the University of 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 , 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://healthtruthrhttp://healthttp://heahttp://he & & page=news_

(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 _http://www.youtube.http://wwwhttp://www.yo_

(http://www.youtube.com/watch?v=85tgwh3HpsM) ; 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 them; 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.http://videhttp://vidhttp://video.<WBhttp://vi_

(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. (In

fact, this

pathogenic mycoplasma has actually been PATENTED by Dr. Shyn Ching Lo of the

American Registry of Pathology in Washington, DC, patent # 5,242,820). As

explained in my document " Inoculation the True Weapons of Mass Destruction " at

_www.drcarley.www_ (http://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 attacks the

myelin sheath (causing demyelination) Although Dr Wakefield did not realize

that

these viruses' significance as a chronic infection is that this leads to a

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 bacteria & 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) I also quote from on's in my CDC

response the symptoms of subacute sclerosing 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 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, and states that the

child has " a regressive encephalopathy with features of autism spectrum

disorder " . Where this mitochondrial defect originated is not discussed...

Where this

mitochondrial defect originated is not discussed...<WBR>injection of foreign

DNA in prior vaccines i (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

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.republichttp://www.rehttp://wwwhttp://www.repubhttp:/ & ProgramID=36 & y\

ear=8 & month=3 & backURL=index.backURL=indebackURL=index

backURL=index.<WbackURL=indexbackURL=indbackURL=inbackURL=indebackURL=index.<W

back_

(http://www.republicbroadcasting.org/index.php?cmd=archives.month & ProgramID=36 & y\

ear=8 & month=3 & backURL=index.php%3Fcmd%3Darchives.getyear%26ProgramID%3

D36 & year=8 & backURL=index.php%3Fcmd%3Darchives)

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 by Jesuit Del Rio, 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 document to Dr. Boyd Haley (_behaley@..._ (mailto:behaley@...) )

and Kirby (_brook200@..._ (mailto:brook200@...) );

please do so yourselves.

Let's roll....

Namaste,

Dr Carley

--

_www.drcarley.www_ (http://www.drcarley.com/)

Listen to " What's Ailing America? " every Thursday night at 8:00 PM EST on

_www.bbsradio.www_ (http://www.bbsradio.com/) and also on

_www.republicbroadcawww.repub_ (http://www.republicbroadcasting.org/) at 12

noon EST every

Wednesday

" Inoculations are the true weapons of mass destruction, causing an epidemic

of genocide "

Carley, MD

Court Qualified Expert in vaccine Induced Diseases

" The individual is handicapped by coming face to face with a conspiracy so

monstrous that he cannot believe it exists "

J Edgar Hoover

FBI Director

All TRUTH passes through 3 stages:

1st - it is ridiculed

2nd - it is violently opposed

3rd - it is accepted as SELF EVIDENT

Arthur Schopenhauer

In a time of universal deceit, telling the TRUTH is a revolutionary act.

1984, Orwell

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[Guest guest]

Thanks for this post.

>

>

>

> PERMISSION BY DR. CARLEY TO REPOST FREELY:

>

> Dr Carley critiques the Fed Ct decision admitting vaccine caused

autism

>

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

knees,

> and the holocaust of 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 encourage of all you to

go to

> _http://www.drcarleyhttp://wwhttp://www.dhtt_

> (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 in

November

> of 2007 in a Court of Federal Claims case brought by neurologist

Dr. Jon

> Poling and his wife claiming that vaccines were the cause of

their daughter

> Hannah's autism. This decision is posted on Kirby's blog at

>

_http://www.huffingthttp://www.http://www.hhttp://www.huffihttp://wwht

tp://www.h_

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

_b_88558.html) .

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

individuals who is

> 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 _www.drcarley.www_

> (http://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

germs 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.drcarleyhttp://www.http://wwwhttp://www_

> (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.huffingthttp://www.http://www.hhttp://www.http://wwhttp://

www.hufhttp_

> (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. More

> confusion and distraction.<WBR>..rather than admitting that there

is no such

> thing as a safe vaccine...and the practice should be abandoned

altogether,

> with attention instead pla 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 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). As explained in the quotes

from

> on's Principles of Medicine, 6th edition, p. 943 posted in

my response to the

> CDC on _www.drcarley.www_ (http://www.drcarley.com/) , " 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. "

>

> 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 at

> _http://www.cdc.http://www.cdhttp://wwhttp://wwwhttp://www._

> (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 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). You can read how DNA

vaccines cause

> genetic mutations at

>

_http://sciamdigitalhttp://sciahttp://sciamdihttp://sciamdigihttp://sc

ia_

> (http://sciamdigital.com/index.cfm?

fa=Search.ViewSearchForItemResultList) (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 MOST

GENETIC

> MUTATIONS IN PEOPLE AND IN PETS; 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

Poling 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 would prove that autism is actually a non-fatal form of

subacute

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

done). However,

> it is a known fact that the measles virus has similar proteins to

myelin

> basic protein, and thus through molecular mimicry, the anti-

measles antibody

> itself can cause demyelination; and, as quoted from on'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)...

>

> IN THE UNITED STATES COURT OF FEDERAL CLAIMS

> OFFICE OF SPECIAL MASTERS

>

>

> CHILD [Hannah Poling], a minor,

>

> by her Parents and Natural Guardians [Dr. & Mrs. Jon Poling],

>

> 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 " ) 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

>

> 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 i

> rritable 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.

reported

> that after CHILD's immunizations of July 19, 2000,

an " encephalopathy progressed

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

and

> relatedness.<WBR> " Id. He noted a disruption in CHILD's sleep

patterns, persistent

> screaming an

>

> would not make eye contact. Id. He diagnosed CHILD

with " regressive

> encephalopathy with features consistent with an autistic spectrum

disorder, following

> normal development. would not make eye contact. Id. He diagnosed

CHILD with

> " regressive encephalopathy with features consistent with an a

would not make

>

> 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 accord

> ance with 42 U.S.C. § 300aa-11©( In sum

>

> 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://healthtruthrhttp://healthttp://healthtruhttp_

> (http://healthtruthrevealed.com/audio-interviews.php) , click

on " inoculations the

> true weapons of mass destruction " , click on " inoculations the true

weapons of

> mass destruction " <WBR> You will hear interviewer Greg Ciola

mention research

> done at the University of 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 , 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://healthtruthrhttp://healthttp://heahttp://he & & page=news_

> (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 _http://www.youtube.http://wwwhttp://www.yo_

> (http://www.youtube.com/watch?v=85tgwh3HpsM) ; 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 them; 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.http://videhttp://vidhttp://video.<WBhttp://vi_

(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. (In fact, this

> pathogenic mycoplasma has actually been PATENTED by Dr. Shyn Ching

Lo of the

> American Registry of Pathology in Washington, DC, patent #

5,242,820). As

> explained in my document " Inoculation the True Weapons of Mass

Destruction " at

> _www.drcarley.www_ (http://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

attacks the

> myelin sheath (causing demyelination) Although Dr Wakefield did not

realize that

> these viruses' significance as a chronic infection is that this

leads to a

> 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 bacteria & 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) I also quote from

on's in my CDC

> response the symptoms of subacute sclerosing 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 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, and states

that the

> child has " a regressive encephalopathy with features of autism

spectrum

> disorder " . Where this mitochondrial defect originated is not

discussed... Where this

> mitochondrial defect originated is not discussed...<WBR>injection

of foreign

> DNA in prior vaccines i (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

> 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.republichttp://www.rehttp://wwwhttp://www.repubhttp:/ & Prog

ramID=36 & year=8 & month=3 & backURL=index.backURL=indebackURL=index

>

backURL=index.<WbackURL=indexbackURL=indbackURL=inbackURL=indebackURL=

index.<W

> back_

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

cmd=archives.month & ProgramID=36 & year=8 & month=3 & backURL=index.php%

3Fcmd%3Darchives.getyear%26ProgramID%3

> D36 & year=8 & backURL=index.php%3Fcmd%3Darchives)

> 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 by Jesuit Del Rio, 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 document to Dr. Boyd Haley (_behaley@..._

(mailto:behaley@...) )

> and Kirby (_brook200@..._ (mailto:brook200@...) );

> please do so yourselves.

>

> Let's roll....

>

> Namaste,

> Dr Carley

>

> --

> _www.drcarley.www_ (http://www.drcarley.com/)

>

> Listen to " What's Ailing America? " every Thursday night at 8:00 PM

EST on

> _www.bbsradio.www_ (http://www.bbsradio.com/) and also on

> _www.republicbroadcawww.repub_

(http://www.republicbroadcasting.org/) at 12 noon EST every

> Wednesday

>

> " Inoculations are the true weapons of mass destruction, causing an

epidemic

> of genocide "

> Carley, MD

> Court Qualified Expert in vaccine Induced Diseases

>

> " The individual is handicapped by coming face to face with a

conspiracy so

> monstrous that he cannot believe it exists "

> J Edgar Hoover

> FBI Director

>

> All TRUTH passes through 3 stages:

> 1st - it is ridiculed

> 2nd - it is violently opposed

> 3rd - it is accepted as SELF EVIDENT

> Arthur Schopenhauer

>

> In a time of universal deceit, telling the TRUTH is a

revolutionary act.

> 1984, Orwell

>

> WARNING

> Any attempts to intercept this message are in violation of Title

18 U.S.C.

> 2511(1) of the

> Electronic Communications Privacy Act (ECPA). All violators are

> subject to fines, imprisonment or civil damages, or both.

>

>

>

>

>

> " Medical research has made such progress, that there are

practically no

> healthy people any more. " †" Aldous Huxley

>

> " ....Perfume to you, to me is excrement. " - Pope

>

>

> I will not have my life narrowed down

> . I will not bow down to somebody else's whim or to someone

else's

> ignorance. -bell hooks

>

>

>

> **************It's Tax Time! Get tips, forms, and advice on AOL

Money &

> Finance. (http://money.aol.com/tax?NCID=aolprf00030000000001)

>

>

>

[Guest guest]

This is a lot of information but worth reading. The problem I have

with the Kirby vs. Dr. Carley issue is that they are both

fighting for the same side yet bickering about the exact cause or

wording of autism (mercury vs. the actual vaccination as being the

actual cause) and other specific illnesses but what if they are both

right and mercury plus the vaccination are both the cause of autism?

The bottom line is that the mercury is a toxin (poison) that I have

no doubt helps contribute to the breakdown of cells which causes all

kind of health issues and the vaccination itself is clearly equally

as bad for our immunity, etc. Instead of people and doctors who are

on the same side battling it out over which specifically caused the

autism (whether it is the actual vaccination or the mercury or both)

maybe they should be coming together to educate the parents and the

public that about all vaccinations, flu shots, etc. destroy your

health and can cause not just autism but many other illnesses as well.

For me as a parent and someone who is ill from mercury poisoning as

well as mold poisoning and many other toxins, including lead, I just

want people to be educated about how deceitful our government is. And

our government somehow needs to be stopped!

Hopefully this makes sense and I got my point across..

Dana

>

>

>

> PERMISSION BY DR. CARLEY TO REPOST FREELY:

>

> Dr Carley critiques the Fed Ct decision admitting vaccine caused

autism

>

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

knees,

> and the holocaust of 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 encourage of all you to

go to

> _http://www.drcarleyhttp://wwhttp://www.dhtt_

> (http://www.drcarley.com/the_big_picture.jpg) ; you will see that

[Guest guest]

I agree Dana. Why all the lies from the government? They are

protecting the pharmaceutical companies for sure. They need to let the

truth come out. One of the parents of this child was a neurologist but

the neurologist I saw didn't want to have a clue. He diagnosed me with

migraine headaches even though it was accompanied with nausea,

dizziness, loss of memory and flu like symptoms.

For me as a parent and someone who is ill from mercury poisoning as

> well as mold poisoning and many other toxins, including lead, I just

> want people to be educated about how deceitful our government is. And

> our government somehow needs to be stopped!

>

> Hopefully this makes sense and I got my point across..

>

> Dana