Cause of Autism Discovered…and it’s Not the Mercury !!!

Cause Of Autism Discovered……And It’s Not The Mercury!

Posted by: “Eric WhoRU”


Mon Mar 10, 2008 7:31 pm (PDT)

Cause Of Autism Discovered……
And It’s Not The Mercury!
By: Dr. Rebecca CarleySource: http://www.drcarley.comMarch 8, 2008

This is the update that has gone out to the thousands of people on my
list. I await the response of David Kirby and Dr Boyd Haley, who are
receiving this e-mail as well.

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 all of you to go to 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

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 David Kirby’s blog at
_b_88558.html. David 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 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 David Kirby on a radio show which is posted on my
website at, 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
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 are 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

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

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
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)…


CHILD, a minor,

by her Parents and Natural Guardians,






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


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, Maryland, for well-child
examinations and minor complaints, including fever and eczema. Pet.
Ex. 31 at 5-10, 19. During this time period, she received the
following pediatric 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 Howard County Infants and Toddlers
Program, on November 17, 2000, and November 28, 2000, due to concerns
about her language development. Pet. Ex. 19 at 2, 7. The assessment
team observed deficits in CHILD’s communication and social
development. Id. at 6. CHILD’s mother reported that CHILD had become
less responsive to verbal direction in the previous four months and
had lost some language skills. Id. At 2.

On December 21, 2000, CHILD returned to ENT Associates because of 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. Andrew Zimmerman, a pediatric neurologist, evaluated CHILD at the
Kennedy Krieger Children’s Hospital Neurology Clinic (“Krieger
Institute”), on February 8, 2001. Pet. Ex. 25 at 1. Dr. Zimmerman
reported that after CHILD’s 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. Richard 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. John 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 occasional 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 Scottish Rite Hospital. Id. at 39, 44. She experienced
no more seizures while at Scottish Rite Hospital and was discharged
on the medications Trileptal and Diastal. Id. at 44. A follow-up MRI
of the brain, on June 16, 2006, was normal with evidence of a left
mastoiditis manifested by distortion of the air cells. Id. at 36. An
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.


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(c)(1)(C)(ii).

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

Respectfully submitted,

Assistant Attorney General

Torts Branch, Civil Division

Deputy Director
Torts Branch, Civil Division

Assistant Director
Torts Branch, Civil Division

s/ Linda S. Renzi by s/ Lynn E. Ricciardella
Senior Trial Counsel
Torts Branch, Civil Division
U.S. Department of Justice
P.O. Box 146
Benjamin Franklin 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, – David Kirby

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

Please go to,
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 John Moore, 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 You
will read on page 16 that Mr. Moore 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. Moore
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
also notice that these neurons in a culture dish do not have myelin
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
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, 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 Andrew Wakefield, whose medical
license was attacked because he demonstrated measles virus in the
lymphoid patches in the guts of autistic children. DR. BOYD ADMITS
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 Harrison’s principles of medicine in my response to the
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 Harrison’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
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.
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
would stop vaccine production altogether, which would stop the
creation of all autoimmune diseases and cancer, which would shut down
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 gohere
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
(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
VIDS. Let’s roll….

Dr Carley


1 Comment (+add yours?)

  1. Miller
    Mar 12, 2008 @ 11:10:24

    Isn’t it true that both you and Kirby have some key points to argue about our children being infected. Why is it a MUST that our children be vaccinated?

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