Re: THE CAUSE OF AUTISM DISCOVERED

[Guest guest]

Is there an age range for children for this?

Thanks

In a message dated 7/18/2010 9:12:43 A.M. Pacific Daylight Time,

shoemakerlinda@... writes:

A huge lawsuit for personal injuries to the children of autism in America

is

underway now that the cause is determined to be mercury, lead poisoning

and

pesticide residues to the center cortex (behavioral center) by assorted

internationally sold Gerber baby foods and certain infant formulas (see

FDA Food

Analyte Matrix Report for " America's Most Dangeorus Foods " , the two lists

you

need to learn more than 50 assorted foods have mercury, lead poisoning and

pesticide residues contained inside Mei Ling's MERCURY IN BABY FOODS: WHAT

THE

FDA KEPT FROM THE WORLD OF AUTISM. All parties need to send your names

and

addresses to The Houser Country Estate, 1520 Meadowbrook Lane,

Mountainview,

Hickory, North Carolina 28602.)

Anywhere Gerber goes, that's where autism is but you need TWO FDA reports

for

the lawsuit. Get the book wholesale while they last at www.Xlibris.com

under

" Mercury in Baby Foods, " avoiding any infant formula found to be

contaminated by

mercury or radium (the FDA lying about 731 foods contaminated by " iodine, "

determined to be a physical impossibility now).

As there is a current FDA report in the book, now you can use BOTH LISTS

to

avoid all foods (table foods such as a tomato or egg) currently not

FEDERALLY

RECALLED. Your child can get new symptoms if he continues to try to grow

a

reasoning center in his brain (pineal gland) and eat mercury, so that's

what the

mystery is all about with children not getting cured as fast as Mr. Raun

Kaufman

of The Autism Treatment Center of America, see book and movie named

" SonRise:

The Miracle Happens. "

Good luck, replies to all letters by post forthcoming to divert you to a

personal injury attorney to sue THE FDA for failure to recall dangerous

substances causing an epidemic actually known as MINAMATA'S DISEASE, the

symptoms the same as what you call " autism, " see the book mentioned.

________________________________

From: Viswadeepa Das <_viswa_das@..._ (mailto:viswa_das@...) >

_ _

(mailto: )

Sent: Sun, July 18, 2010 11:48:36 AM

Subject: Re: [ ] Re: Chelation question - Seizure & normal

EEG -

Andy please

Hello Andy,

Thank you so much.

We will insist for the meds or find someone else who will since we want to

start

chelation ASAP.

Regards.

Deepa.

From: andrewhallcutler <_AndyCutler@..._ (mailto:AndyCutler@...) >

Subject: [ ] Re: Chelation question - Seizure & normal EEG -

Andy

please

_ _

(mailto: )

Date: Sunday, July 18, 2010, 4:33 AM

The EEG report doesn't look very thorough to me. Generally they recite all

kinds

of stuff they did not see, and describe what they did see in more detail.

They no doubt didn't see a seizure on it, but most of the time they don't

-

especially when they have to sedate the patient and don't have cooperation.

If you can, get the trace and show it to every doc you see in hopes one

knows

how to interpret them and will discuss it with you. It might contain

useful

information.

You might also ask the doc who took it to show you it and a completely

normal

one, e. g. in a textbook, and explain any differences you see.

As it is, you have a kid who had 2 seizures but an uninformative EEG. The

most

common result from an EEG on an epileptic is no seizures are observed.

Most

medical books do suggest a trial of antiepileptic drug (AED) therapy under

these

circumstances of 2 seizures but none seen on EEG.

Also, for non-talkers, the most likely intervention to make them talk is

an AED.

It isn't a high probability, but I have been diligently collecting stories

of

what worked for kids who just don't talk and that is one of the few things

with

any real likelihood of doing so.

Seems to me insisting on a trial of an AED makes some sense. If the doctor

doesn't want to do it, try finding a real doctor instead of an

oppositional

gatekeeper.

Since the EEG wasn't reported as having any information at all, and you

didn't

get any discussion from the doctor of what sort of thing it might be, you

don't

have much to go on for what sort of AED might work. Depakote is probably

the

most broad spectrum, and has a very substantial side effect and risk

profile,

but at least it is old enough that the risks are well known. Neurontin is

very

low risk but least likely to work. Lamictal is newer and supposedly less

risk

but it does have substantial risks and they're less well understood.

The one thing you can be sure of - if you don't use an AED, and also don't

chelate him, nothing is going to get better.

Andy

_http://www.noamalgam.com/index.html_ (http://www.noamalgam.com/index.html)

Amalgam Illness: Diagnosis and Treatment

_http://www.noamalgam.com/hairtestbook.html_

(http://www.noamalgam.com/hairtestbook.html)

Hair Test Interpretation: Finding Hidden Toxicities

_http://www.noamalgam.com/nourishinghope.html_

(http://www.noamalgam.com/nourishinghope.html)

Nourishing Hope for Autism: Nutrition Intervention for Healing Our Children

_http://www.noamalgam.com/biologicaltreatments.html_

(http://www.noamalgam.com/biologicaltreatments.html)

Biological Treatments for Autism and PDD

>

> We started AC chelation for our 13.5 yr old, 98 lbs, non-verbal,

diagnosed

>severely autistic son with 12.5mg ALA and DMSA in May.

>

>

> During the first round after the 2nd dose, he had a grand mal seizure

for the

>first time in his life and we stopped the round. Subsequently he had

another

>similar seizure after 3 weeks.

>

> We saw a Pediatric Neurologist and an EEG was done. The EEG report came

>'normal'. The report can be viewed here.

>

> _http://www.scribd.com/doc/34474553/Rik-EEG-Jun-2010_

(http://www.scribd.com/doc/34474553/Rik-EEG-Jun-2010)

>

> Since the EEG came clean, the doctor does not want to start any seizure

>medication. And as I understand from Andy's book, older posts and other

>experienced parents, it is not advisable to start chelating without

seizure meds

>in place.

>

> We are scheduled to see the doctor for a follow-up on the 21st. What

should we

>do ?

>

> Will be extremely grateful for your advice. Kindly respond.

> Regards,

>

> Deepa.

>

>

>

>

>

>

>

> [Non-text portions of this message have been removed]

>

[Non-text portions of this message have been removed]

[Non-text portions of this message have been removed]

[Guest guest]

A huge lawsuit for personal injuries to the children of autism in America is

underway now that the cause is determined to be mercury, lead poisoning and

pesticide residues to the center cortex (behavioral center) by assorted

internationally sold Gerber baby foods and certain infant formulas (see FDA Food

Analyte Matrix Report for " America's Most Dangeorus Foods " , the two lists you

need to learn more than 50 assorted foods have mercury, lead poisoning and

pesticide residues contained inside Mei Ling's MERCURY IN BABY FOODS: WHAT THE

FDA KEPT FROM THE WORLD OF AUTISM.  All parties need to send your names and

addresses to The Houser Country Estate, 1520 Meadowbrook Lane, Mountainview,

Hickory, North Carolina 28602.)

Anywhere Gerber goes, that's where autism is but you need TWO FDA reports for

the lawsuit.  Get the book wholesale while they last at www.Xlibris.com under

" Mercury in Baby Foods, " avoiding any infant formula found to be contaminated by

mercury or radium (the FDA lying about 731 foods contaminated by " iodine, "

determined to be a physical impossibility now).

As there is a current FDA report in the book, now you can use BOTH LISTS to

avoid all foods (table foods such as a tomato or egg) currently not FEDERALLY

RECALLED.  Your child can get new symptoms if he continues to try to grow a

reasoning center in his brain (pineal gland) and eat mercury, so that's what the

mystery is all about with children not getting cured as fast as Mr. Raun Kaufman

of The Autism Treatment Center of America, see book and movie named " SonRise:

The Miracle Happens. "

Good luck, replies to all letters by post forthcoming to divert you to a

personal injury attorney to sue THE FDA for failure to recall dangerous

substances causing an epidemic actually known as MINAMATA'S DISEASE, the

symptoms the same as what you call " autism, " see the book mentioned.

________________________________

From: Viswadeepa Das <viswa_das@...>

Sent: Sun, July 18, 2010 11:48:36 AM

Subject: Re: [ ] Re: Chelation question - Seizure & normal EEG -

Andy please

 

Hello Andy,

 

Thank you so much.

 

We will insist for the meds or find someone else who will since we want to start

chelation ASAP.

 

Regards.

 

Deepa.

From: andrewhallcutler <AndyCutler@...>

Subject: [ ] Re: Chelation question - Seizure & normal EEG - Andy

please

Date: Sunday, July 18, 2010, 4:33 AM

 

The EEG report doesn't look very thorough to me. Generally they recite all kinds

of stuff they did not see, and describe what they did see in more detail.

They no doubt didn't see a seizure on it, but most of the time they don't -

especially when they have to sedate the patient and don't have cooperation.

If you can, get the trace and show it to every doc you see in hopes one knows

how to interpret them and will discuss it with you. It might contain useful

information.

You might also ask the doc who took it to show you it and a completely normal

one, e. g. in a textbook, and explain any differences you see.

As it is, you have a kid who had 2 seizures but an uninformative EEG. The most

common result from an EEG on an epileptic is no seizures are observed. Most

medical books do suggest a trial of antiepileptic drug (AED) therapy under these

circumstances of 2 seizures but none seen on EEG.

Also, for non-talkers, the most likely intervention to make them talk is an AED.

It isn't a high probability, but I have been diligently collecting stories of

what worked for kids who just don't talk and that is one of the few things with

any real likelihood of doing so.

Seems to me insisting on a trial of an AED makes some sense. If the doctor

doesn't want to do it, try finding a real doctor instead of an oppositional

gatekeeper.

Since the EEG wasn't reported as having any information at all, and you didn't

get any discussion from the doctor of what sort of thing it might be, you don't

have much to go on for what sort of AED might work. Depakote is probably the

most broad spectrum, and has a very substantial side effect and risk profile,

but at least it is old enough that the risks are well known. Neurontin is very

low risk but least likely to work. Lamictal is newer and supposedly less risk

but it does have substantial risks and they're less well understood.

The one thing you can be sure of - if you don't use an AED, and also don't

chelate him, nothing is going to get better.

Andy

http://www.noamalgam.com/index.html

Amalgam Illness: Diagnosis and Treatment

http://www.noamalgam.com/hairtestbook.html

Hair Test Interpretation: Finding Hidden Toxicities

http://www.noamalgam.com/nourishinghope.html

Nourishing Hope for Autism: Nutrition Intervention for Healing Our Children

http://www.noamalgam.com/biologicaltreatments.html

Biological Treatments for Autism and PDD

>

> We started AC chelation for our 13.5 yr old, 98 lbs, non-verbal, diagnosed

>severely autistic son with 12.5mg ALA and DMSA in May.

>

>

> During the first round after the 2nd dose, he had a grand mal seizure for the

>first time in his life and we stopped the round. Subsequently he had another

>similar seizure after 3 weeks.

>

> We saw a Pediatric Neurologist and an EEG was done. The EEG report came

>'normal'. The report can be viewed here.

>

> http://www.scribd.com/doc/34474553/Rik-EEG-Jun-2010

>

> Since the EEG came clean, the doctor does not want to start any seizure

>medication. And as I understand from Andy's book, older posts and other

>experienced parents, it is not advisable to start chelating without seizure

meds

>in place.

>

> We are scheduled to see the doctor for a follow-up on the 21st. What should we

>do ?

>

> Will be extremely grateful for your advice. Kindly respond.

> Regards,

>

> Deepa.

>

>

>

>

>

>

>

>