Re: Cause Of Autism Discovered......And It's Not The Mercury!

[Guest guest]

So, if Dr Carley is accurate, do we forget about chelation? What

else do we need to do to help our kids. Does Dr Carley have the

answer?

>

> We thank Dr. Carley for being consistant on speaking the full

truth, that vaccines belong in the garbage can! She explains in

detail how vaccines destroy the immune system and I encourage you to

spread the word to everyone you know. The truth is coming out and

together we WILL make a difference, April

>

> By: Dr. Carley

> Source: http://www.drcarley.com

> March 8, 2008

> http://www.healthtruthrevealed.com/full-page.php?

id=1500256603 & & page=article

>

> VIC (Vaccine Injuried Children)

> Autism is 1 in 150 children today and it's impossible to have a

genetic epidemic!

> Please learn from our mistake and educate BEFORE you vaccinate!

> For more information visit www.vacinfo.org or call 800-939-8227

>

[Guest guest]

I've listened to quite a few online recordings with Dr. Carley and

respect her knowledge but all people, not just autistic ones are toxic

these days and everyone, those who are not healthy and those who

appear to be should be getting metals out of their body.

Our family did homeopathy for years and while we had some limited

results, we kept reverting back to bad health. Only when the mercury

was out did we see REAL and lasting improvements. One and half years

and no reversals in symptoms have occurred.

Toxins are not the only problem with autism but they do play a huge

role as I'm sure we're all aware of. I would do both homeopathy and

chelation for autism. Dr. Carley does consultations. You can't get

the type of remedies/nosodes she recommends from the health food store

so a consult is imperative. This is not a do-it-yourself scenario.

Sharon Hoehner

> >

> > We thank Dr. Carley for being consistant on speaking the full

> truth, that vaccines belong in the garbage can! She explains in

> detail how vaccines destroy the immune system and I encourage you to

> spread the word to everyone you know. The truth is coming out and

> together we WILL make a difference, April

> >

> > By: Dr. Carley

> > Source: http://www.drcarley.com

> > March 8, 2008

> > http://www.healthtruthrevealed.com/full-page.php?

> id=1500256603 & & page=article

> >

> > VIC (Vaccine Injuried Children)

> > Autism is 1 in 150 children today and it's impossible to have a

> genetic epidemic!

> > Please learn from our mistake and educate BEFORE you vaccinate!

> > For more information visit www.vacinfo.org or call 800-939-8227

> >

>

[Guest guest]

If you read her website, you will see that she believes autism is from

the virus in the vaccine and that mercury is very bad and causes other

problems and must be detoxed also.

She just wants the word out that vaccines are not safe if the mercury

is removed. barb

-- In , " VIC " <VIC@...> wrote:

>

> We thank Dr. Carley for being consistant on speaking the full truth,

that vaccines belong in the garbage can! She explains in detail how

vaccines destroy the immune system and I encourage you to spread the

word to everyone you know. The truth is coming out and together we

WILL make a difference, April

>

> By: Dr. Carley

> Source: http://www.drcarley.com

> March 8, 2008

>

http://www.healthtruthrevealed.com/full-page.php?id=1500256603 & & page=article

>

> VIC (Vaccine Injuried Children)

> Autism is 1 in 150 children today and it's impossible to have a

genetic epidemic!

> Please learn from our mistake and educate BEFORE you vaccinate!

> For more information visit www.vacinfo.org or call 800-939-8227

>

[Guest guest]

I agree with you Sharon! It's just that our kids got the worse of it,

but there are a lot of people ill because of all the toxins they are

exposed to.

Zurama

> > >

> > > We thank Dr. Carley for being consistant on speaking the full

> > truth, that vaccines belong in the garbage can! She explains in

> > detail how vaccines destroy the immune system and I encourage you to

> > spread the word to everyone you know. The truth is coming out and

> > together we WILL make a difference, April

> > >

> > > By: Dr. Carley

> > > Source: http://www.drcarley.com

> > > March 8, 2008

> > > http://www.healthtruthrevealed.com/full-page.php?

> > id=1500256603 & & page=article

> > >

> > > VIC (Vaccine Injuried Children)

> > > Autism is 1 in 150 children today and it's impossible to have a

> > genetic epidemic!

> > > Please learn from our mistake and educate BEFORE you vaccinate!

> > > For more information visit www.vacinfo.org or call 800-939-8227

> > >

> >

>

[Guest guest]

No we don't necessarily forget about chelation. It is not that simple.

If you go to Dr. Carley's website and look at her four flowcharts and

her overview of what is causing the modern epidemic of disease,

mercury is a factor but it is not the whole story.

This coincides exactly with my experiences. I am still chelating

(myself, adult), but I now know that there is another component, not

just the metals. It is viral. It is immune dysfunction. And I believe

Dr. Carley is right on the money with her theory that the vaccinations

corrupt the immune system.

BTW I am a long time member but rarely post anymore. I have two

children with autism-like syndromes and other allergic/autoimmune

problems. I will try to post again here and there to let you know how

I do with Dr. Carley's protocol as I will begin it soon.

Arlene

> >

> > We thank Dr. Carley for being consistant on speaking the full

> truth, that vaccines belong in the garbage can! She explains in

> detail how vaccines destroy the immune system and I encourage you to

> spread the word to everyone you know. The truth is coming out and

> together we WILL make a difference, April

> >

> > By: Dr. Carley

> > Source: http://www.drcarley.com

> > March 8, 2008

> > http://www.healthtruthrevealed.com/full-page.php?

> id=1500256603 & & page=article

> >

> > VIC (Vaccine Injuried Children)

> > Autism is 1 in 150 children today and it's impossible to have a

> genetic epidemic!

> > Please learn from our mistake and educate BEFORE you vaccinate!

> > For more information visit www.vacinfo.org or call 800-939-8227

> >

>

[Guest guest]

I think thimerosal trips the immune system and the live viruses slip

by. Most kids are affected by mercury, but for a variety of factors

not all get rid of it right away. It gets into the brain and won't

come out.

I don't know of Dr. Carley, but she certainly doesn't approve of

mercury.

> >

> > We thank Dr. Carley for being consistant on speaking the full

> truth, that vaccines belong in the garbage can! She explains in

> detail how vaccines destroy the immune system and I encourage you

to

> spread the word to everyone you know. The truth is coming out and

> together we WILL make a difference, April

> >

> > By: Dr. Carley

> > Source: http://www.drcarley.com

> > March 8, 2008

> > http://www.healthtruthrevealed.com/full-page.php?

> id=1500256603 & & page=article

> >

> > VIC (Vaccine Injuried Children)

> > Autism is 1 in 150 children today and it's impossible to have a

> genetic epidemic!

> > Please learn from our mistake and educate BEFORE you vaccinate!

> > For more information visit www.vacinfo.org or call 800-939-8227

> >

>

[Guest guest]

Can this be forwarded?

-

VIC <VIC@...> wrote:

Please accept my apology if you have already received this, but there was an

error in the email program and many did not receive this very important message.

We thank Dr. Carley for being consistant on speaking the full truth, that

vaccines belong in the garbage can! She explains in detail how vaccines destroy

the immune system and I encourage you to spread the word to everyone you know.

The truth is coming out and together we WILL make a difference, April

SPECIAL REPORT!

Cause Of Autism Discovered......

And It's Not The Mercury!

By: Dr. Carley

Source: http://www.drcarley.com

March 8, 2008

This is the update that has gone out to the thousands of people on my list. I

await the response of 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

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.html.

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 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 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

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 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

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 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=36 & ye\

ar=8 & month=3 & backURL=index.php%253Fcmd%253Darchives.getyear%2526ProgramID%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. Let's roll....

Namaste,

Dr Carley

VIC (Vaccine Injuried Children)

Autism is 1 in 150 children today and it's impossible to have a genetic

epidemic!

Please learn from our mistake and educate BEFORE you vaccinate!

For more information visit www.vacinfo.org or call 800-939-8227

" The fool says in his heart, 'There is no God'. " [Psalm 14:1]

_._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._.

Is HBOT at your hospital?

http://apps.nlm.nih.gov/medlineplus/directories/index.cfm

EPSDT decisions http://healthlaw.org/pubs/200308.epsdtdocket.html

Unrestricted downloads of 50+ pdf files on HBOT efficacy

medicaid/files/ ,

2/files/ and

http://www.drneubauerhbo.com/papers.htm

Download your state EPSDT program http://www.hcfa.gov/medicaid/stateplan/Map.asp

by doing a search on the word " ameliorate " . State Medicaid websites

http://www.medi-cal.ca.gov/RelSites_Oth_States.asp . Medicaid waiver programs:

http://www.geocities.com/HotSprings/Villa/1029/medicaid.html

Find a hyperbaric clinic http://www.netnet.net/mums/hbolistAK-FL.htm,

http://www.netnet.net/mums/hbolistGA-NC.htm,

http://www.netnet.net/mums/hbolistOH-WI.htm

HBOT can save billions of dollars and millions of heartaches.

http://www. .com

[Guest guest]

I've done about 70 rounds of chelation with Andy's protocol over 3+

years and have much improvement but still no speech. My son was more

or less a vegetable before we started chelating and he's a lot better

but still very much autistic.

Can anyone briefly describe how Dr Carly's ideas might help.

> > >

> > > We thank Dr. Carley for being consistant on speaking the full

> > truth, that vaccines belong in the garbage can! She explains in

> > detail how vaccines destroy the immune system and I encourage you

to

> > spread the word to everyone you know. The truth is coming out

and

> > together we WILL make a difference, April

> > >

> > > By: Dr. Carley

> > > Source: http://www.drcarley.com

> > > March 8, 2008

> > > http://www.healthtruthrevealed.com/full-page.php?

> > id=1500256603 & & page=article

> > >

> > > VIC (Vaccine Injuried Children)

> > > Autism is 1 in 150 children today and it's impossible to have a

> > genetic epidemic!

> > > Please learn from our mistake and educate BEFORE you vaccinate!

> > > For more information visit www.vacinfo.org or call 800-939-8227

> > >

> >

>

[Guest guest]

Have you done any anti-viral therapy?

Best Jr <bettwice33@...> wrote: I've done about 70 rounds of

chelation with Andy's protocol over 3+

years and have much improvement but still no speech. My son was more

or less a vegetable before we started chelating and he's a lot better

but still very much autistic.

Can anyone briefly describe how Dr Carly's ideas might help.

> > >

> > > We thank Dr. Carley for being consistant on speaking the full

> > truth, that vaccines belong in the garbage can! She explains in

> > detail how vaccines destroy the immune system and I encourage you

to

> > spread the word to everyone you know. The truth is coming out

and

> > together we WILL make a difference, April

> > >

> > > By: Dr. Carley

> > > Source: http://www.drcarley.com

> > > March 8, 2008

> > > http://www.healthtruthrevealed.com/full-page.php?

> > id=1500256603 & & page=article

> > >

> > > VIC (Vaccine Injuried Children)

> > > Autism is 1 in 150 children today and it's impossible to have a

> > genetic epidemic!

> > > Please learn from our mistake and educate BEFORE you vaccinate!

> > > For more information visit www.vacinfo.org or call 800-939-8227

> > >

> >

>

=======================================================

[Guest guest]

Well, first I will say I have yet to begin her protocol. However, I

understand it to work by systematically removing the toxins that

corrupt the immune system. She focuses on those introduced via

vaccinations, and says that the media used to culture the viruses must

also be detoxed out because you can never separate the media (i.e. the

monkey kidney and rabit spinal column, etc..) from the rest of the

stuff in the vaccination. And this is in part what causees the

autoimmunity---the viral stimulus and the other toxins are introduced

along with these tissues and the immune system is essentially taught

to recognize these tissues as foreign. She also uses supplements to

support the immune system and she deals with other toxins besides thos

e in vaccines. The detox is done with homeopathic nosodes. This is

basically it in a nutshell, as I understand it. I like you have seen

tremendous progress with chelation but I now must face it that I will

never get to the finish-line with chelation alone. This protocol makes

logical and scientific sense; so I am prepared to give it a shot. Oh,

also, chelation can supposedly be done homeopathically. I have heard

that before but never really thought it could download the amount of

metals I was dealing with, but now my metals load is low, and we shall

see.

> > > >

> > > > We thank Dr. Carley for being consistant on speaking the full

> > > truth, that vaccines belong in the garbage can! She explains in

> > > detail how vaccines destroy the immune system and I encourage you

> to

> > > spread the word to everyone you know. The truth is coming out

> and

> > > together we WILL make a difference, April

> > > >

> > > > By: Dr. Carley

> > > > Source: http://www.drcarley.com

> > > > March 8, 2008

> > > > http://www.healthtruthrevealed.com/full-page.php?

> > > id=1500256603 & & page=article

> > > >

> > > > VIC (Vaccine Injuried Children)

> > > > Autism is 1 in 150 children today and it's impossible to have a

> > > genetic epidemic!

> > > > Please learn from our mistake and educate BEFORE you vaccinate!

> > > > For more information visit www.vacinfo.org or call 800-939-8227

> > > >

> > >

> >

>

[Guest guest]

No, no anti-virals. I don't know what it is. What drugs are

involved?

> > > >

> > > > We thank Dr. Carley for being consistant on speaking the full

> > > truth, that vaccines belong in the garbage can! She explains in

> > > detail how vaccines destroy the immune system and I encourage

you

> to

> > > spread the word to everyone you know. The truth is coming out

> and

> > > together we WILL make a difference, April

> > > >

> > > > By: Dr. Carley

> > > > Source: http://www.drcarley.com

> > > > March 8, 2008

> > > > http://www.healthtruthrevealed.com/full-page.php?

> > > id=1500256603 & & page=article

> > > >

> > > > VIC (Vaccine Injuried Children)

> > > > Autism is 1 in 150 children today and it's impossible to have

a

> > > genetic epidemic!

> > > > Please learn from our mistake and educate BEFORE you

vaccinate!

> > > > For more information visit www.vacinfo.org or call 800-939-

8227

> > > >

> > >

> >

>

>

>

>

> =======================================================

>

[Guest guest]

You do not have to use drugs neccessarily. I myself plan on using Dana's method

of Olive Leaf Extract, Virastop, lyseine, vitamin C and vitamin A. All of these

are natural antivirals that can be found at a health food store. The OLE and

virastop are supposed to be pretty powerful products. My son has only completed

4 full rounds of chelation so I probably will wait a while before adding the

viral protocol in. Since you have already done so many rounds I think you should

give it a shot. Some kids need the anti-viral therapy for speech.

This is a link to Dana's website about what helped her kids with speech. I

find she's usually right on the money when it comes to treating autism.

http://www.danasview.net/issues.htm

By the way, DAN docs use Valtrex to control the viruses as well as other Rx

medications, so you could go that route too.

Best Wishes,

Maggie

Best Jr <bettwice33@...> wrote:

No, no anti-virals. I don't know what it is. What drugs are

involved?

> > > >

> > > > We thank Dr. Carley for being consistant on speaking the full

> > > truth, that vaccines belong in the garbage can! She explains in

> > > detail how vaccines destroy the immune system and I encourage

you

> to

> > > spread the word to everyone you know. The truth is coming out

> and

> > > together we WILL make a difference, April

> > > >

> > > > By: Dr. Carley

> > > > Source: http://www.drcarley.com

> > > > March 8, 2008

> > > > http://www.healthtruthrevealed.com/full-page.php?

> > > id=1500256603 & & page=article

> > > >

> > > > VIC (Vaccine Injuried Children)

> > > > Autism is 1 in 150 children today and it's impossible to have

a

> > > genetic epidemic!

> > > > Please learn from our mistake and educate BEFORE you

vaccinate!

> > > > For more information visit www.vacinfo.org or call 800-939-

8227

> > > >

> > >

> >

>

>

>

>

> =======================================================

>

[Guest guest]

Some have also used Virastop and others have used Valtrex to deal

with viruses. Check the archives and information here and at these

.

Enzymes and Autism

http://tinyurl.com/3x6ouo

MB12 Valtrex

http://tinyurl.com/3atkpx

> >

> > Have you done any anti-viral therapy?

[Guest guest]

As someone who has been observing this dialogue about 'its not the

mercury' I'd like to remind the readers of this discussion that those

in the community from Safeminds to Kirby have never said that

it was ONLY the mercury. In fact, it is only a part of the

discussion, but it is an important part of the discussion because of

the harmful nature of mercury. Three prevailing topics in the

Congressional investigation looking at vaccine injury leading to

autism came up - (1) that MMR as a live virus vaccine lead to measles

encephalopathy and/or to a low level measles infection that remained

in the body (2) that mercury as a preservative and an ingredient used

in the development of vaccines caused direct injury and/or disrupted

the body's immune function or exacerbated other underlying conditions

(there seemed to be some similarities in the family medical

histories - such as auto-immune disorders such as rhematoid

arthritis, lupus; a history of frequent ear infections and heavy use

of antibiotics) the child often had bowel conditions, frquent yeast

outbreaks and viruses. A third an underlying discussion that is

related not only to autism is that more children that medical

professionals recognize have adverse events and that the incidents

are often not documented or acknowledged. The arched back, incessant

screaming, and lack of focus after immunization was not widely

discussed before the Congressional investigation (and the work of the

NVIC) brought it forward. What the mercury/autism communtiy has done

is continue to fight for the removal of a neurotoxin that we know

adversely affects mitochondria and can lead to brain injury, they

have also worked hard to remind the world that there is a lot we

don't know about vaccination. For those who think for instance that

Kirby ONLY discusses mercury, then please go to his website and

review his slide show and listen to one of his public speeches....he

actually does a very good job of discussing a lot of other issues.

Mercury, whether in a vaccine, a lightbulb, paint, fish, or household

cleaner, has no place in our homes. The risks outweigh the benefit

and care needs to be taken to assure that those who are most

vulnerable are protected.

> > >

> > > Have you done any anti-viral therapy?

>

[Guest guest]

>

> I've done about 70 rounds of chelation with Andy's protocol over 3+

> years and have much improvement but still no speech.

Chelation allowed my son to tolerate supplements, it was the

supplements that caused speech. I wrote here what my son needed

http://www.danasview.net/supps.htm

The most important supps for speech were anti-virals [OLE, Virastop,

vitamin C, lysine, and I also did high dose vitamin A for measles

virus], mB12/TMG/folic/carnitine, mito cocktail and EFAs, and biotin

and GSE to control yeast.

>> My son was more

> or less a vegetable before we started chelating and he's a lot better

> but still very much autistic.

This is a good description of my son. The only real benefit of

chelation [i used ALA] that was obvious, is that it allowed him to

tolerate foods and supps. It was the supps that caused him to lose

his dx.

Dana

[Guest guest]

accummulative contributing factors. My acquired newest " catch phrase "

for the mess of all of this " stuff. " It all totally bites, imho. And

it feels like it is all connected. " all " of it. " any " of it.

just adding two cents to the mix Aarrghh Land - me, just gonna

plant my butt there. every time I think my " visit " is done, an info

slam will send me right back. and I think that that is just crazy. a

topsy turvy world going on and I am not liking that at all. (where else

am I gonna live??? yk?)

wishing all the very best answers

elizabeth

[Guest guest]

Dana and all, Thanks, I'll try the sup's.

> >

> > I've done about 70 rounds of chelation with Andy's protocol over

3+

> > years and have much improvement but still no speech.

>

>

> Chelation allowed my son to tolerate supplements, it was the

> supplements that caused speech. I wrote here what my son needed

>

> http://www.danasview.net/supps.htm

>

> The most important supps for speech were anti-virals [OLE, Virastop,

> vitamin C, lysine, and I also did high dose vitamin A for measles

> virus], mB12/TMG/folic/carnitine, mito cocktail and EFAs, and biotin

> and GSE to control yeast.

>

>

> >> My son was more

> > or less a vegetable before we started chelating and he's a lot

better

> > but still very much autistic.

>

>

> This is a good description of my son. The only real benefit of

> chelation [i used ALA] that was obvious, is that it allowed him to

> tolerate foods and supps. It was the supps that caused him to lose

> his dx.

>

> Dana

>

[Guest guest]

If its not the mercury, why is chelation working so well for my child?

Best Jr wrote:

>

> So, if Dr Carley is accurate, do we forget about chelation? What

> else do we need to do to help our kids. Does Dr Carley have the

> answer?

>

>

> >

> > We thank Dr. Carley for being consistant on speaking the full

> truth, that vaccines belong in the garbage can! She explains in

> detail how vaccines destroy the immune system and I encourage you to

> spread the word to everyone you know. The truth is coming out and

> together we WILL make a difference, April

> >

> > By: Dr. Carley

> > Source: http://www.drcarley.com <http://www.drcarley.com>

> > March 8, 2008

> > http://www.healthtruthrevealed.com/full-page.php?

> <http://www.healthtruthrevealed.com/full-page.php?>

> id=1500256603 & & page=article

> >

> > VIC (Vaccine Injuried Children)

> > Autism is 1 in 150 children today and it's impossible to have a

> genetic epidemic!

> > Please learn from our mistake and educate BEFORE you vaccinate!

> > For more information visit www.vacinfo.org or call 800-939-8227

> >

>

>

[Guest guest]

ps to my post...I do believe, and this is pure opinion on my part, that

mercury is the biggest contributing factor, for us. In info slams, I

find the " other " contributing factors, that these are what explain

the " why's. " Why the effect on one child, is more vestibular, and in

another, I see the peeling skin, and the other one tends to lethargy,

while these two over here can't sleep, the one who bounces off all the

walls, and the other two who will not leave their rooms, the two who

are prone to obsessions, the one who cannot stray from his " set "

schedule, and the one who is chaos revisited....I can link our

exposures to mercury, whether it is fillings, shots, pesticides - to

the " worst " years and all the concurrent " worst " symptoms - concurrent

for all - that is what is most striking to me, while I attempt to piece

together all these puzzle pieces of " crap & yet more crap " (big sigh,

apologies - can't come up with ANY acceptable words for that

one)....and the myriad symptoms, that can ALL be explained by the

effects of mercury - these combined with each person's individual

previous/concurrent exposures to other toxins, especially during baby

and toddler years & their own individual responses...the mercury

connections, this makes it all make much more sense. Mercury is not the

only contributing factor...but it is a biggee, no doubts about it, in

my mind.

fwiw

wishing all the very best answers

elizabeth

>

> accummulative contributing factors. My acquired newest " catch phrase "

> for the mess of all of this " stuff. " It all totally bites, imho. And

> it feels like it is all connected. " all " of it. " any " of it.

>

> just adding two cents to the mix Aarrghh Land - me, just gonna

> plant my butt there. every time I think my " visit " is done, an info

> slam will send me right back. and I think that that is just crazy. a

> topsy turvy world going on and I am not liking that at all. (where

else

> am I gonna live??? yk?)

>

> wishing all the very best answers

> elizabeth

>

[Guest guest]

What I can't understand is the strong upheld belief that it is either - or.

Everybody who researches vaccines will come across information on the

devastating effect to them in general. Even without a single atom of mercury

they would still do harm. Dr Carley is right in this respect, but to dismiss

the role of mercury all together is simply not scientific (i.e.seeking for

the truth). The neurotoxic effects of mercury are almost identical to

symptoms in autism.

My own interest in autism started when I had a loading with a mercury

compound that caused symptoms, many of which had striking similarities to

those in autism.

Dorothee

On Sun, Mar 9, 2008 at 10:19 PM, VIC <VIC@...> wrote:

> Please accept my apology if you have already received this, but there was

> an error in the email program and many did not receive this very important

> message.

>

> We thank Dr. Carley for being consistant on speaking the full truth, that

> vaccines belong in the garbage can! She explains in detail how vaccines

> destroy the immune system and I encourage you to spread the word to everyone

> you know. The truth is coming out and together we WILL make a difference,

> April

>

> SPECIAL REPORT!

> Cause Of Autism Discovered......

> And It's Not The Mercury!

> By: Dr. Carley

> Source: http://www.drcarley.com

> March 8, 2008

>

> This is the update that has gone out to the thousands of people on my

> list. I await the response of 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

> 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.html.

> 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<http://www.huffingtonpost.com/david-kirby/government-concedes-vacci_b_8\

8323.html%29....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 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 102.3degrees

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 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 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 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 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=36 & ye\

ar=8 & month=3 & backURL=index.php%253Fcmd%253Darchives.getyear%2526ProgramID%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. Let's roll....

>

> Namaste,

> Dr Carley

>

>

>

> VIC (Vaccine Injuried Children)

> Autism is 1 in 150 children today and it's impossible to have a genetic

> epidemic!

> Please learn from our mistake and educate BEFORE you vaccinate!

> For more information visit www.vacinfo.org or call 800-939-8227

>

>

>

>

> =======================================================

>

[Guest guest]

Helllo

On 23/03/2008, Dorothee Krien <dorotheekrien@...> wrote:

> What I can't understand is the strong upheld belief that it is either - or.

Same here i can be a number of things. Personally i think people

predisposed to autism have leaky guts that allow mercury and live

vaccines to enter and posion the brain and other organs. The

bloodstream links many organs together which is how the mercury and

live vaccines are transmitted.

>

> Everybody who researches vaccines will come across information on the

> devastating effect to them in general. Even without a single atom of mercury

> they would still do harm. Dr Carley is right in this respect, but to dismiss

> the role of mercury all together is simply not scientific (i.e.seeking for

> the truth).

Agreed, even dismissing the leaky gut theory of autism is wrong. Im

annoyed at the BBC for publishing such an article. Gluten and milk

free diets helped me because im addicted to the opiate effects of

them. Even lactose can affect me.

> The neurotoxic effects of mercury are almost identical to symptoms in autism.

Its very interesting that you mention that as some autistic people

claim chelation only works (they havent tried it) because the people

were mercury poisoned not because they had autism.

>

> My own interest in autism started when I had a loading with a mercury

> compound that caused symptoms, many of which had striking similarities to

> those in autism.

>

> Dorothee

>

--

is

[Guest guest]

Hi Dorothee,

In my experience, people generally want to simplify things and

frequently look for " the smoking gun " -- i.e. some singular cause to

blame.

Something I wrote on this list previously that you might like/agree

with: http://onibasu.com/archives/am/177172.html

Michele

www.HealthGazelle.org

www.KidsLikeMine.org

>

> What I can't understand is the strong upheld belief that it is

either - or.

>

> Everybody who researches vaccines will come across information on

the

> devastating effect to them in general. Even without a single atom

of mercury

> they would still do harm. Dr Carley is right in this respect, but

to dismiss

> the role of mercury all together is simply not scientific

(i.e.seeking for

> the truth). The neurotoxic effects of mercury are almost identical

to

> symptoms in autism.

>

> My own interest in autism started when I had a loading with a

mercury

> compound that caused symptoms, many of which had striking

similarities to

> those in autism.

>

> Dorothee

>

>

[Guest guest]

Hello

On 23/03/2008, Michele <talithamichele@...> wrote:

> Hi Dorothee,

> In my experience, people generally want to simplify things and

> frequently look for " the smoking gun " -- i.e. some singular cause to

> blame.

> Something I wrote on this list previously that you might like/agree

> with: http://onibasu.com/archives/am/177172.html

i enjoyed your comments especially the encouraging advice about

tolerating certain foods/supplements. i hope to go back on milk (even

goats milk) in a few years time

post chelation.

>

> Michele

> www.HealthGazelle.org

> www.KidsLikeMine.org

>

> --- In , " Dorothee Krien "

>

is

[Guest guest]

I think autism is multi causal in that we have more environmental

toxins, nutrition in food has deteriorated, vaccines increased, and

people's bodies to detoxify dwindled. I also think my family had the

extra cause of being predispositioned to " autoimmune disease " such as

allergies and asthma.

This is the theory I believe in and I got it from a book by Dr Bock

that specializes with autism, asthma, allergies, and adhd.

Kay

[Guest guest]

Hello

On 23/03/2008, Kay <knorgren@...> wrote:

> I think autism is multi causal in that we have more environmental

> toxins, nutrition in food has deteriorated, vaccines increased, and

> people's bodies to detoxify dwindled. I also think my family had the

> extra cause of being predispositioned to " autoimmune disease " such as

> allergies and asthma.

>

> This is the theory I believe in and I got it from a book by Dr Bock

> that specializes with autism, asthma, allergies, and adhd.

Can you send me the link please? i could hire the book from the library, cheers

is

>

>

> Kay