Re: Can someone get these links to McCarthy-- this kid is dying

[Guest guest]

Please someone help!!I don't know if the following

info willhelp,but at the very least they should NOT

have to pay an attorney!!!!

Disability Rights Education and Defense Fund Inc.

Primary Address: 2212 6th St

City: Berkeley

State: CA

Zipcode: 94710-2219

General Phone: 510-644-2555

Fax: 510-841-8645

Counties Served: Nationwide

Case Types: Education, Individual Rights

Other Case Types: Civil Rights, Disability

Web Site: http://www.dredf.org

--- anacat_11 <anacat_11@...> wrote:

> Can Horton hear a Who?

>

> The time to take action on this is running out. The

> family is in

> Orange County. Maybe someone in California will care

> enough to help.

> The family's lawyer, whom they can scarcely afford,

> is not making

> headway and they cannot even get a specialist onto

> the Fairview

> institution grounds to check the boy's condition.

> The boy was sent to

> the stroke unit in ER some weeks ago because the

> drugs the

> institution is forcing on him are killing him. The

> institution

> snatched him right back out of trauma unit and then

> increased all his

> doses to the maximum. The description of Nate's

> condition by his

> father in the post below is hard to read, but bear

> in mind that the

> situation has gotten worse.

>

>

> http://www.getnatehome.com/in_the_media

> http://www.getnatehome.com

>

> Dear friends. We received very bad news for Nate and

> our family from

> the Fairview administration and the doctor today.

> These people are

> enforcing our son on Geodon - psychotropic drug

> which is extremely

> harmful and poisonous for our son. They are starting

> this drug from

> today evening. They took our son from home

> completely physically

> healthy and since they started him on different

> psychotropic drugs

> against his will and his family he developed Grand

> Mal seizures -

> epilepsy. These drugs don't have any medical merit.

> They are used as

> chemical restrains which are additional to physical

> restrains used on

> him often.It is against medical advice from a number

> of the doctors

> including medical experts in neurology. It is not

> ethical practice of

> medicine. It is not necessary. Our son who was very

> energetic before

> is spending all his days in the bed as the result of

> the harmful

> drugs they impose on him earlier. From the

> psychotropic drugs our son

> was delivered in critical condition numbers of time

> to the emergency

> room of the different hospital. Last time he was

> admitted to

> the Hoag Hospital emergency room with epileptic

> seizures after he was

> enforced to psychotropic drug as the punishment and

> chemical

> restrains to the behaviors which our son doesn't

> have control because

> of his sensory issue and his response to his

> isolation, harmful

> drugs, and the environment since he removed from his

> family. We sow

> in the hospital his reactions on this poisonous

> drugs which his

> body do not accept. He was having terrible pains,

> his body was all

> red, his breathing was stopping and his heart rate

> was high when his

> blood pressure was low. We days and nights were

> sitting at his bed in

> the stroke unit of the hospital. Since this day

> January 21, 2008 our

> son is different. He looks like he suffered stroke

> or brain damage

> because his speech is blurred, his coordination is

> unstable, his

> memory and eyes visions is effected. We came to this

> country to

> live dissent life, free of the suppression.

>

>

>

>

________________________________________________________________________________\

____

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know-it-all with Mobile. Try it now.

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[Guest guest]

Anacat, myself, and others on this list have been trying to get help for this

family for

weeks. They are having trouble getting a donation link/site up and running for

Nate. I

have an attorney who contacted me today from COPAA (A California organization of

parents, advocates, and attorneys) interested in taking Nate's case, and no one

has

contacted me. I have spoken to his mother who is pleading for help and the

situation with

Nate's meds and I am doing all I can ( I have two kids that are injured). I have

contacted all

of my representatives and their staff that I know, and found that they have to

go through

" casework " , which apparently is not an option.

This is a horrible situation, and I am a little disappointed with other CA orgs

that I have

contacted and have not responded.

King

>

> > Can Horton hear a Who?

> >

> > The time to take action on this is running out. The

> > family is in

> > Orange County. Maybe someone in California will care

> > enough to help.

> > The family's lawyer, whom they can scarcely afford,

> > is not making

> > headway and they cannot even get a specialist onto

> > the Fairview

> > institution grounds to check the boy's condition.

> > The boy was sent to

> > the stroke unit in ER some weeks ago because the

> > drugs the

> > institution is forcing on him are killing him. The

> > institution

> > snatched him right back out of trauma unit and then

> > increased all his

> > doses to the maximum. The description of Nate's

> > condition by his

> > father in the post below is hard to read, but bear

> > in mind that the

> > situation has gotten worse.

> >

> >

> > http://www.getnatehome.com/in_the_media

> > http://www.getnatehome.com

> >

> > Dear friends. We received very bad news for Nate and

> > our family from

> > the Fairview administration and the doctor today.

> > These people are

> > enforcing our son on Geodon - psychotropic drug

> > which is extremely

> > harmful and poisonous for our son. They are starting

> > this drug from

> > today evening. They took our son from home

> > completely physically

> > healthy and since they started him on different

> > psychotropic drugs

> > against his will and his family he developed Grand

> > Mal seizures -

> > epilepsy. These drugs don't have any medical merit.

> > They are used as

> > chemical restrains which are additional to physical

> > restrains used on

> > him often.It is against medical advice from a number

> > of the doctors

> > including medical experts in neurology. It is not

> > ethical practice of

> > medicine. It is not necessary. Our son who was very

> > energetic before

> > is spending all his days in the bed as the result of

> > the harmful

> > drugs they impose on him earlier. From the

> > psychotropic drugs our son

> > was delivered in critical condition numbers of time

> > to the emergency

> > room of the different hospital. Last time he was

> > admitted to

> > the Hoag Hospital emergency room with epileptic

> > seizures after he was

> > enforced to psychotropic drug as the punishment and

> > chemical

> > restrains to the behaviors which our son doesn't

> > have control because

> > of his sensory issue and his response to his

> > isolation, harmful

> > drugs, and the environment since he removed from his

> > family. We sow

> > in the hospital his reactions on this poisonous

> > drugs which his

> > body do not accept. He was having terrible pains,

> > his body was all

> > red, his breathing was stopping and his heart rate

> > was high when his

> > blood pressure was low. We days and nights were

> > sitting at his bed in

> > the stroke unit of the hospital. Since this day

> > January 21, 2008 our

> > son is different. He looks like he suffered stroke

> > or brain damage

> > because his speech is blurred, his coordination is

> > unstable, his

> > memory and eyes visions is effected. We came to this

> > country to

> > live dissent life, free of the suppression.

> >

> >

> >

> >

>

>

>

>

________________________________________________________________________________\

____

> Be a better friend, newshound, and

> know-it-all with Mobile. Try it now.

http://mobile./;_ylt=Ahu06i62sR8HDtDypao8Wcj9tAcJ

>

[Guest guest]

I'll try some CA orgs tomorrow.

--- King <medfordkings1@...> wrote:

> Anacat, myself, and others on this list have been

> trying to get help for this family for

> weeks. They are having trouble getting a donation

> link/site up and running for Nate. I

> have an attorney who contacted me today from COPAA

> (A California organization of

> parents, advocates, and attorneys) interested in

> taking Nate's case, and no one has

> contacted me. I have spoken to his mother who is

> pleading for help and the situation with

> Nate's meds and I am doing all I can ( I have two

> kids that are injured). I have contacted all

> of my representatives and their staff that I know,

> and found that they have to go through

> " casework " , which apparently is not an option.

>

> This is a horrible situation, and I am a little

> disappointed with other CA orgs that I have

> contacted and have not responded.

>

> King

>

>

> >

> > > Can Horton hear a Who?

> > >

> > > The time to take action on this is running out.

> The

> > > family is in

> > > Orange County. Maybe someone in California will

> care

> > > enough to help.

> > > The family's lawyer, whom they can scarcely

> afford,

> > > is not making

> > > headway and they cannot even get a specialist

> onto

> > > the Fairview

> > > institution grounds to check the boy's

> condition.

> > > The boy was sent to

> > > the stroke unit in ER some weeks ago because the

> > > drugs the

> > > institution is forcing on him are killing him.

> The

> > > institution

> > > snatched him right back out of trauma unit and

> then

> > > increased all his

> > > doses to the maximum. The description of Nate's

> > > condition by his

> > > father in the post below is hard to read, but

> bear

> > > in mind that the

> > > situation has gotten worse.

> > >

> > >

> > > http://www.getnatehome.com/in_the_media

> > > http://www.getnatehome.com

> > >

> > > Dear friends. We received very bad news for Nate

> and

> > > our family from

> > > the Fairview administration and the doctor

> today.

> > > These people are

> > > enforcing our son on Geodon - psychotropic drug

> > > which is extremely

> > > harmful and poisonous for our son. They are

> starting

> > > this drug from

> > > today evening. They took our son from home

> > > completely physically

> > > healthy and since they started him on different

> > > psychotropic drugs

> > > against his will and his family he developed

> Grand

> > > Mal seizures -

> > > epilepsy. These drugs don't have any medical

> merit.

> > > They are used as

> > > chemical restrains which are additional to

> physical

> > > restrains used on

> > > him often.It is against medical advice from a

> number

> > > of the doctors

> > > including medical experts in neurology. It is

> not

> > > ethical practice of

> > > medicine. It is not necessary. Our son who was

> very

> > > energetic before

> > > is spending all his days in the bed as the

> result of

> > > the harmful

> > > drugs they impose on him earlier. From the

> > > psychotropic drugs our son

> > > was delivered in critical condition numbers of

> time

> > > to the emergency

> > > room of the different hospital. Last time he was

> > > admitted to

> > > the Hoag Hospital emergency room with epileptic

> > > seizures after he was

> > > enforced to psychotropic drug as the punishment

> and

> > > chemical

> > > restrains to the behaviors which our son doesn't

> > > have control because

> > > of his sensory issue and his response to his

> > > isolation, harmful

> > > drugs, and the environment since he removed from

> his

> > > family. We sow

> > > in the hospital his reactions on this poisonous

> > > drugs which his

> > > body do not accept. He was having terrible

> pains,

> > > his body was all

> > > red, his breathing was stopping and his heart

> rate

> > > was high when his

> > > blood pressure was low. We days and nights were

> > > sitting at his bed in

> > > the stroke unit of the hospital. Since this day

> > > January 21, 2008 our

> > > son is different. He looks like he suffered

> stroke

> > > or brain damage

> > > because his speech is blurred, his coordination

> is

> > > unstable, his

> > > memory and eyes visions is effected. We came to

> this

> > > country to

> > > live dissent life, free of the suppression.

> > >

> > >

> > >

> > >

> >

> >

> >

> >

>

________________________________________________________________________________\

____

> > Be a better friend, newshound, and

> > know-it-all with Mobile. Try it now.

>

http://mobile./;_ylt=Ahu06i62sR8HDtDypao8Wcj9tAcJ

> >

>

>

>

>

________________________________________________________________________________\

____

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[Guest guest]

Well, TACA responded immediately with referrals and a supportive

email, and some professionals have made contact with the Tseglins.

But more is needed to fight the racket that Fairview has going. It's

like they're on a quest to kill the child.

So I know what you mean. I don't get why there hasn't been more

response. The family has had to borrow money to hire the attorney

they have and are in dire straits to hire a qualified neurologist or

reform psychiatrist to see Nate. The instituation won't let the

family's choice of doctor in to see Nate anyway and their current

attorney doesn't seem to have an answer for this, though I don't know

what happened to today or what will happen tomorrow. I wonder if what

the family needs is press, press, press and someone with serious

clout and visibility to take up the cause. The institution holding

the boy is pure evil.

>

> Anacat, myself, and others on this list have been trying to get

help for this family for

> weeks. They are having trouble getting a donation link/site up and

running for Nate. I

> have an attorney who contacted me today from COPAA (A California

organization of

> parents, advocates, and attorneys) interested in taking Nate's

case, and no one has

> contacted me. I have spoken to his mother who is pleading for help

and the situation with

> Nate's meds and I am doing all I can ( I have two kids that are

injured). I have contacted all

> of my representatives and their staff that I know, and found that

they have to go through

> " casework " , which apparently is not an option.

>

> This is a horrible situation, and I am a little disappointed with

other CA orgs that I have

> contacted and have not responded.

>

> King

>

>

[Guest guest]

Thank you, , you're a doll!

>

[Guest guest]

I am glad to hear that TACA responded. We do need press coverage on this. I have

contacted all of my press contacts and more (I am in Northern California), but

no one

wants to cover this. I have spoke to people with the SacBee, local news

stations, the Contra

Costa Times, etc.. No one will cover this. This family really needs an advocate

versed in the

type of chemical abuse that Nate is going through, but I don't know if it's

going to happen.

> >

> > Anacat, myself, and others on this list have been trying to get

> help for this family for

> > weeks. They are having trouble getting a donation link/site up and

> running for Nate. I

> > have an attorney who contacted me today from COPAA (A California

> organization of

> > parents, advocates, and attorneys) interested in taking Nate's

> case, and no one has

> > contacted me. I have spoken to his mother who is pleading for help

> and the situation with

> > Nate's meds and I am doing all I can ( I have two kids that are

> injured). I have contacted all

> > of my representatives and their staff that I know, and found that

> they have to go through

> > " casework " , which apparently is not an option.

> >

> > This is a horrible situation, and I am a little disappointed with

> other CA orgs that I have

> > contacted and have not responded.

> >

> > King

> >

> >

>

[Guest guest]

How can publications not cover this?

In this correspondence I had with a psychopharmaceutical expert, she

wrote the creepiest thing about her experience as a plaintiff expert

witness against Eli Lilly for a drug injury or death suit. I don't

think she's normally prone to dramatic language or religious

reference. She was deposed five times, for eight hours at a stretch

by Lilly attorneys and wrote,

" They are evil. I mean it.

They are the Devil. "

Well, maybe the Devil's gotten into the press.

> > >

> > > Anacat, myself, and others on this list have been trying to get

> > help for this family for

> > > weeks. They are having trouble getting a donation link/site up

and

> > running for Nate. I

> > > have an attorney who contacted me today from COPAA (A

California

> > organization of

> > > parents, advocates, and attorneys) interested in taking Nate's

> > case, and no one has

> > > contacted me. I have spoken to his mother who is pleading for

help

> > and the situation with

> > > Nate's meds and I am doing all I can ( I have two kids that are

> > injured). I have contacted all

> > > of my representatives and their staff that I know, and found

that

> > they have to go through

> > > " casework " , which apparently is not an option.

> > >

> > > This is a horrible situation, and I am a little disappointed

with

> > other CA orgs that I have

> > > contacted and have not responded.

> > >

> > > King

> > >

> > >

> >

>

[Guest guest]

I agree. It might have something to do with me hammering them with the Poling

case, but

I doubt it, as this preempted my request for them to cover the Tsegins. In both

cases, I

either got, " I am stacked up with work, I just don't have the time " , or " This is

100 miles out

of our viewer demographic-my editors would never let me run the story " .

> > > >

> > > > Anacat, myself, and others on this list have been trying to get

> > > help for this family for

> > > > weeks. They are having trouble getting a donation link/site up

> and

> > > running for Nate. I

> > > > have an attorney who contacted me today from COPAA (A

> California

> > > organization of

> > > > parents, advocates, and attorneys) interested in taking Nate's

> > > case, and no one has

> > > > contacted me. I have spoken to his mother who is pleading for

> help

> > > and the situation with

> > > > Nate's meds and I am doing all I can ( I have two kids that are

> > > injured). I have contacted all

> > > > of my representatives and their staff that I know, and found

> that

> > > they have to go through

> > > > " casework " , which apparently is not an option.

> > > >

> > > > This is a horrible situation, and I am a little disappointed

> with

> > > other CA orgs that I have

> > > > contacted and have not responded.

> > > >

> > > > King

> > > >

> > > >

> > >

> >

>