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

March 6, 2008

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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March 6, 2008