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"On top of this, we moved into a new house over the weekend, and I'm 30 weeks pregnant with another daughter whom I'm fearful will also have some kind developmental disorders since these things tend to run in families. "

-

Hi! Just a note of encouragement! We have 4 children. Our 2nd child, 1st dd is the one with autism. The rest of the children are fine.

ElaineF

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I didn't mention that. I gave my youngest 2 hib shots. This is when he

lost skills and started self stimming and prompted me to start the diet with

him. I would recommend no vaccinations also.

Dawn

>

>Reply-To: Autism_in_Girls

>To: <Autism_in_Girls >

>Subject: Re: (unknown)

>Date: Wed, 20 Jun 2001 10:28:25 -0700

>

>Consider not vaccinating your new baby?

>Kathy

> (unknown)

>

>

> > Yesterday my world turned upside down and inside out. My 23-

> > month old daughter was diagnosed with mild to moderate autism. A

> > very good child psychiatrist with the Children's Health Council near

> > Stanford University diagnosed her, so I have little reason to doubt

> > her.

> >

> > The doctor said it's good that we caught it early, and hopefully my

> > daughter, Chloe will have a pretty bright future.

> >

> > On top of this, we moved into a new house over the weekend, and I'm

> > 30 weeks pregnant with another daughter whom I'm fearful will also

> > have some kind developmental disorders since these things tend to run

> > in families.

> >

> > I feel very bad for Chloe since I know that social awkwardness is

> > less tolerated in girls than it is in boys. And since adolescents is

> > always hard on so called normal girls, I can't imagine to think of

> > what it will be with a girl with autism.

> >

> > Is there any information out there on how to deal with females with

> > autism as opposed to just boys?

> >

> > Our doctor recommended the LOVAAS approach for 25 hours a week. And

> > while I agree with trying this therapy, I can't help thinking that

> > this poor kid is barely two, and she already has a job.

> >

> > Thank you for listening to me rant.

> >

> >

> >

> >

> >

> >

> >

> >

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Guest guest

I didn't mention that. I gave my youngest 2 hib shots. This is when he

lost skills and started self stimming and prompted me to start the diet with

him. I would recommend no vaccinations also.

Dawn

>

>Reply-To: Autism_in_Girls

>To: <Autism_in_Girls >

>Subject: Re: (unknown)

>Date: Wed, 20 Jun 2001 10:28:25 -0700

>

>Consider not vaccinating your new baby?

>Kathy

> (unknown)

>

>

> > Yesterday my world turned upside down and inside out. My 23-

> > month old daughter was diagnosed with mild to moderate autism. A

> > very good child psychiatrist with the Children's Health Council near

> > Stanford University diagnosed her, so I have little reason to doubt

> > her.

> >

> > The doctor said it's good that we caught it early, and hopefully my

> > daughter, Chloe will have a pretty bright future.

> >

> > On top of this, we moved into a new house over the weekend, and I'm

> > 30 weeks pregnant with another daughter whom I'm fearful will also

> > have some kind developmental disorders since these things tend to run

> > in families.

> >

> > I feel very bad for Chloe since I know that social awkwardness is

> > less tolerated in girls than it is in boys. And since adolescents is

> > always hard on so called normal girls, I can't imagine to think of

> > what it will be with a girl with autism.

> >

> > Is there any information out there on how to deal with females with

> > autism as opposed to just boys?

> >

> > Our doctor recommended the LOVAAS approach for 25 hours a week. And

> > while I agree with trying this therapy, I can't help thinking that

> > this poor kid is barely two, and she already has a job.

> >

> > Thank you for listening to me rant.

> >

> >

> >

> >

> >

> >

> >

> >

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Guest guest

I didn't mention that. I gave my youngest 2 hib shots. This is when he

lost skills and started self stimming and prompted me to start the diet with

him. I would recommend no vaccinations also.

Dawn

>

>Reply-To: Autism_in_Girls

>To: <Autism_in_Girls >

>Subject: Re: (unknown)

>Date: Wed, 20 Jun 2001 10:28:25 -0700

>

>Consider not vaccinating your new baby?

>Kathy

> (unknown)

>

>

> > Yesterday my world turned upside down and inside out. My 23-

> > month old daughter was diagnosed with mild to moderate autism. A

> > very good child psychiatrist with the Children's Health Council near

> > Stanford University diagnosed her, so I have little reason to doubt

> > her.

> >

> > The doctor said it's good that we caught it early, and hopefully my

> > daughter, Chloe will have a pretty bright future.

> >

> > On top of this, we moved into a new house over the weekend, and I'm

> > 30 weeks pregnant with another daughter whom I'm fearful will also

> > have some kind developmental disorders since these things tend to run

> > in families.

> >

> > I feel very bad for Chloe since I know that social awkwardness is

> > less tolerated in girls than it is in boys. And since adolescents is

> > always hard on so called normal girls, I can't imagine to think of

> > what it will be with a girl with autism.

> >

> > Is there any information out there on how to deal with females with

> > autism as opposed to just boys?

> >

> > Our doctor recommended the LOVAAS approach for 25 hours a week. And

> > while I agree with trying this therapy, I can't help thinking that

> > this poor kid is barely two, and she already has a job.

> >

> > Thank you for listening to me rant.

> >

> >

> >

> >

> >

> >

> >

> >

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Hi ,

Sorry to hear about the diagnosis. How mild/severe is your daughter? (What

is her name, by the way?) You did catch it early on. You were also lucky

to find a doc who would dx at that age - - mine would not, even at the age

of 2.5, I guess he's rather old school....

By Stanford - - - I take it you are in the Bay Area? I live in Pleasanton.

You are 30 weeks pregnant. Now is hardly the time to worry about the baby

inside you who is as healthy as can be right now. You can do nothing more

than keep her healthy while in you, and love her just like you loved your 2

year old daughter. While this may " tend' to run in families (and I should

know as I have fraternal twin girls, both with some degree of autism), it is

not common to find a family with more than one child with autism, girls at

that. So rest easy for two reasons: 1. chances are, it's not, and 2. only

God knows, and there is NOTHING you can do about it in the meantime, so you

need not heed another moment's thought on that.

It looks like your doctor has put you on the right track. If you are in the

Bay Area, then I also would advise you to call the Regional Center. They

have some outstanding Early Intervention Services that they can provide for

your daughter until she is age three. We didn't get to utilize any of that,

and I am kicking myself for it now. Let me know if you need a name or

number.

I feel for you, and know how you feel right now. Just hang in there. It

doesn't get right side up anytime too soon, but one does get accustomed to

being upside down, and in time - - - the upside down will feel like right

side up, you'll see.

Grace

(unknown)

> Yesterday my world turned upside down and inside out. My 23-

> month old daughter was diagnosed with mild to moderate autism. A

> very good child psychiatrist with the Children's Health Council near

> Stanford University diagnosed her, so I have little reason to doubt

> her.

>

> The doctor said it's good that we caught it early, and hopefully my

> daughter, Chloe will have a pretty bright future.

>

> On top of this, we moved into a new house over the weekend, and I'm

> 30 weeks pregnant with another daughter whom I'm fearful will also

> have some kind developmental disorders since these things tend to run

> in families.

>

> I feel very bad for Chloe since I know that social awkwardness is

> less tolerated in girls than it is in boys. And since adolescents is

> always hard on so called normal girls, I can't imagine to think of

> what it will be with a girl with autism.

>

> Is there any information out there on how to deal with females with

> autism as opposed to just boys?

>

> Our doctor recommended the LOVAAS approach for 25 hours a week. And

> while I agree with trying this therapy, I can't help thinking that

> this poor kid is barely two, and she already has a job.

>

> Thank you for listening to me rant.

>

>

>

>

>

>

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Guest guest

Hi ,

Sorry to hear about the diagnosis. How mild/severe is your daughter? (What

is her name, by the way?) You did catch it early on. You were also lucky

to find a doc who would dx at that age - - mine would not, even at the age

of 2.5, I guess he's rather old school....

By Stanford - - - I take it you are in the Bay Area? I live in Pleasanton.

You are 30 weeks pregnant. Now is hardly the time to worry about the baby

inside you who is as healthy as can be right now. You can do nothing more

than keep her healthy while in you, and love her just like you loved your 2

year old daughter. While this may " tend' to run in families (and I should

know as I have fraternal twin girls, both with some degree of autism), it is

not common to find a family with more than one child with autism, girls at

that. So rest easy for two reasons: 1. chances are, it's not, and 2. only

God knows, and there is NOTHING you can do about it in the meantime, so you

need not heed another moment's thought on that.

It looks like your doctor has put you on the right track. If you are in the

Bay Area, then I also would advise you to call the Regional Center. They

have some outstanding Early Intervention Services that they can provide for

your daughter until she is age three. We didn't get to utilize any of that,

and I am kicking myself for it now. Let me know if you need a name or

number.

I feel for you, and know how you feel right now. Just hang in there. It

doesn't get right side up anytime too soon, but one does get accustomed to

being upside down, and in time - - - the upside down will feel like right

side up, you'll see.

Grace

(unknown)

> Yesterday my world turned upside down and inside out. My 23-

> month old daughter was diagnosed with mild to moderate autism. A

> very good child psychiatrist with the Children's Health Council near

> Stanford University diagnosed her, so I have little reason to doubt

> her.

>

> The doctor said it's good that we caught it early, and hopefully my

> daughter, Chloe will have a pretty bright future.

>

> On top of this, we moved into a new house over the weekend, and I'm

> 30 weeks pregnant with another daughter whom I'm fearful will also

> have some kind developmental disorders since these things tend to run

> in families.

>

> I feel very bad for Chloe since I know that social awkwardness is

> less tolerated in girls than it is in boys. And since adolescents is

> always hard on so called normal girls, I can't imagine to think of

> what it will be with a girl with autism.

>

> Is there any information out there on how to deal with females with

> autism as opposed to just boys?

>

> Our doctor recommended the LOVAAS approach for 25 hours a week. And

> while I agree with trying this therapy, I can't help thinking that

> this poor kid is barely two, and she already has a job.

>

> Thank you for listening to me rant.

>

>

>

>

>

>

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Guest guest

Hi ,

Sorry to hear about the diagnosis. How mild/severe is your daughter? (What

is her name, by the way?) You did catch it early on. You were also lucky

to find a doc who would dx at that age - - mine would not, even at the age

of 2.5, I guess he's rather old school....

By Stanford - - - I take it you are in the Bay Area? I live in Pleasanton.

You are 30 weeks pregnant. Now is hardly the time to worry about the baby

inside you who is as healthy as can be right now. You can do nothing more

than keep her healthy while in you, and love her just like you loved your 2

year old daughter. While this may " tend' to run in families (and I should

know as I have fraternal twin girls, both with some degree of autism), it is

not common to find a family with more than one child with autism, girls at

that. So rest easy for two reasons: 1. chances are, it's not, and 2. only

God knows, and there is NOTHING you can do about it in the meantime, so you

need not heed another moment's thought on that.

It looks like your doctor has put you on the right track. If you are in the

Bay Area, then I also would advise you to call the Regional Center. They

have some outstanding Early Intervention Services that they can provide for

your daughter until she is age three. We didn't get to utilize any of that,

and I am kicking myself for it now. Let me know if you need a name or

number.

I feel for you, and know how you feel right now. Just hang in there. It

doesn't get right side up anytime too soon, but one does get accustomed to

being upside down, and in time - - - the upside down will feel like right

side up, you'll see.

Grace

(unknown)

> Yesterday my world turned upside down and inside out. My 23-

> month old daughter was diagnosed with mild to moderate autism. A

> very good child psychiatrist with the Children's Health Council near

> Stanford University diagnosed her, so I have little reason to doubt

> her.

>

> The doctor said it's good that we caught it early, and hopefully my

> daughter, Chloe will have a pretty bright future.

>

> On top of this, we moved into a new house over the weekend, and I'm

> 30 weeks pregnant with another daughter whom I'm fearful will also

> have some kind developmental disorders since these things tend to run

> in families.

>

> I feel very bad for Chloe since I know that social awkwardness is

> less tolerated in girls than it is in boys. And since adolescents is

> always hard on so called normal girls, I can't imagine to think of

> what it will be with a girl with autism.

>

> Is there any information out there on how to deal with females with

> autism as opposed to just boys?

>

> Our doctor recommended the LOVAAS approach for 25 hours a week. And

> while I agree with trying this therapy, I can't help thinking that

> this poor kid is barely two, and she already has a job.

>

> Thank you for listening to me rant.

>

>

>

>

>

>

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Guest guest

--Forgive me, this is a bit off the subject, but when i asked

some medically specific ?'s about the immune system's interaction with a

pregnancy, specifically in my miscarriages, the reproductive

endocrinologist raised his eyebrows and went into a long explanation,

intentionally way above my head, about immune dysfunctions that have long

since been disproven, totally unrelated to my ?'s. I find it hard to

believe he was threatened by my knowlege, i certainly wasn't being

arrogant...Wow, glad i'll only have to deal with this guy for a short

time! Makes me appreciate my reg. dr's even more!! Maurita, mom to

Wesley, Iga def, , and

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  • 9 months later...
Guest guest

Hello , my name is Marilyn and I have been with this support group for

approximately 3 three years. I know you will find this site extremely

informative and supportive. Hope you find it a warm and friendly place. Please

feel free to ask any questions as I know there are many people here that would

love to help you.

Take care,

Marilyn

mhogg69@...

(unknown)

Hello, My name is , I'm 26, and was just diagnosed with Stills Disease.

My story is very similar to most of yours. I don't know to much about the

disease yet, just what i have read here. I go for my first follow up exam on

the 30th. I'm hopeing the Dr will be able to offer a lil more information

than what he has already, which has been nothing. This site has been very

helpful not only for me but for my family, in understanding what I am going

through. In reading a lot of your stories i just sat and cried. I would

really love to just talk to someone, so if anyone has time my aol screenname

is Bla5861480, feel free to IM me.

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Guest guest

Hello , my name is Marilyn and I have been with this support group for

approximately 3 three years. I know you will find this site extremely

informative and supportive. Hope you find it a warm and friendly place. Please

feel free to ask any questions as I know there are many people here that would

love to help you.

Take care,

Marilyn

mhogg69@...

(unknown)

Hello, My name is , I'm 26, and was just diagnosed with Stills Disease.

My story is very similar to most of yours. I don't know to much about the

disease yet, just what i have read here. I go for my first follow up exam on

the 30th. I'm hopeing the Dr will be able to offer a lil more information

than what he has already, which has been nothing. This site has been very

helpful not only for me but for my family, in understanding what I am going

through. In reading a lot of your stories i just sat and cried. I would

really love to just talk to someone, so if anyone has time my aol screenname

is Bla5861480, feel free to IM me.

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Guest guest

Dear ,

Welcome to Stilligans Island. It is very nice to meet you. My name is ,

but I am known here as Sue #2. I know that you will find so much helpful

information here , and yes...your family will too. My mother has often read

messages typed by my friends, because she longs to know more about this disease.

My family is very supportive of me. , there are so many people here

experiencing the same pain as you and all the questions. It really helps to

have so many people going through all that you are going through as well. We

have bad days yes....but there are good days too and that is what this group is

all about..support, understanding, trust, knowledge & friendship. If you are

having a bad day, talk to us. There is usually someone always around since we

are all from different time zones. It is very comforting to know that you can

talk to friends at any hour of the day. We love to hear about your good days as

well. It keeps the " hope " here and keeps the energy moving. I am a single mom

of 35 years old with two boys, and trying to manage this disease, work and be

their mom can have its days, but leaning on my friends here helps a lot. They

really understand because they are going through it too. It is a wonderful

support group. I don't know what I would of done without them. I look forward

to talking with you more and update us with your next doctors appointment

if possible.

Sincerely, Sue #2

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Guest guest

Dear ,

Welcome to Stilligans Island. It is very nice to meet you. My name is ,

but I am known here as Sue #2. I know that you will find so much helpful

information here , and yes...your family will too. My mother has often read

messages typed by my friends, because she longs to know more about this disease.

My family is very supportive of me. , there are so many people here

experiencing the same pain as you and all the questions. It really helps to

have so many people going through all that you are going through as well. We

have bad days yes....but there are good days too and that is what this group is

all about..support, understanding, trust, knowledge & friendship. If you are

having a bad day, talk to us. There is usually someone always around since we

are all from different time zones. It is very comforting to know that you can

talk to friends at any hour of the day. We love to hear about your good days as

well. It keeps the " hope " here and keeps the energy moving. I am a single mom

of 35 years old with two boys, and trying to manage this disease, work and be

their mom can have its days, but leaning on my friends here helps a lot. They

really understand because they are going through it too. It is a wonderful

support group. I don't know what I would of done without them. I look forward

to talking with you more and update us with your next doctors appointment

if possible.

Sincerely, Sue #2

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Guest guest

I'm not sure if this is going to go to everyone or just to Marilyn, but i

wanted to thank you for the warm welcome. I'm new to these mass mailings.

So i'm going to send this and see if it goes to everyone or just you..Thanks

again though for making me feel so welcome. These past few weeks have been

rough ones for me and so far the group has really helped out.

>From: mhogg69@...

>Reply-To: Stillsdisease

>To: <Stillsdisease >

>Subject: Re: (unknown)

>Date: Sat, 20 Apr 2002 19:14:30 -0400

>

>Hello , my name is Marilyn and I have been with this support group for

>approximately 3 three years. I know you will find this site extremely

>informative and supportive. Hope you find it a warm and friendly place.

>Please feel free to ask any questions as I know there are many people here

>that would love to help you.

>

>Take care,

>

>Marilyn

>mhogg69@...

> (unknown)

>

>

>

>

> Hello, My name is , I'm 26, and was just diagnosed with Stills

>Disease.

> My story is very similar to most of yours. I don't know to much about

>the

> disease yet, just what i have read here. I go for my first follow up

>exam on

> the 30th. I'm hopeing the Dr will be able to offer a lil more

>information

> than what he has already, which has been nothing. This site has been

>very

> helpful not only for me but for my family, in understanding what I am

>going

> through. In reading a lot of your stories i just sat and cried. I would

> really love to just talk to someone, so if anyone has time my aol

>screenname

> is Bla5861480, feel free to IM me.

>

>

>

>

>

>

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Guest guest

I'm not sure if this is going to go to everyone or just to Marilyn, but i

wanted to thank you for the warm welcome. I'm new to these mass mailings.

So i'm going to send this and see if it goes to everyone or just you..Thanks

again though for making me feel so welcome. These past few weeks have been

rough ones for me and so far the group has really helped out.

>From: mhogg69@...

>Reply-To: Stillsdisease

>To: <Stillsdisease >

>Subject: Re: (unknown)

>Date: Sat, 20 Apr 2002 19:14:30 -0400

>

>Hello , my name is Marilyn and I have been with this support group for

>approximately 3 three years. I know you will find this site extremely

>informative and supportive. Hope you find it a warm and friendly place.

>Please feel free to ask any questions as I know there are many people here

>that would love to help you.

>

>Take care,

>

>Marilyn

>mhogg69@...

> (unknown)

>

>

>

>

> Hello, My name is , I'm 26, and was just diagnosed with Stills

>Disease.

> My story is very similar to most of yours. I don't know to much about

>the

> disease yet, just what i have read here. I go for my first follow up

>exam on

> the 30th. I'm hopeing the Dr will be able to offer a lil more

>information

> than what he has already, which has been nothing. This site has been

>very

> helpful not only for me but for my family, in understanding what I am

>going

> through. In reading a lot of your stories i just sat and cried. I would

> really love to just talk to someone, so if anyone has time my aol

>screenname

> is Bla5861480, feel free to IM me.

>

>

>

>

>

>

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Guest guest

Hello this eve. ; forgive me for not welcoming you sooner. My name is

Patty also Melt :0) I have been busy this weekend but would be pleased to

know you further.

I have had Still's for 25 years and am now going on 44. I am so glad you

found this group and we are willing to share and help in any way we can.

Till soon, Pattymelt

(unknown)

> >

> >

> >

> >

> > Hello, My name is , I'm 26, and was just diagnosed with Stills

> >Disease.

> > My story is very similar to most of yours. I don't know to much about

> >the

> > disease yet, just what i have read here. I go for my first follow up

> >exam on

> > the 30th. I'm hopeing the Dr will be able to offer a lil more

> >information

> > than what he has already, which has been nothing. This site has been

> >very

> > helpful not only for me but for my family, in understanding what I am

> >going

> > through. In reading a lot of your stories i just sat and cried. I

would

> > really love to just talk to someone, so if anyone has time my aol

> >screenname

> > is Bla5861480, feel free to IM me.

> >

> >

> >

> >

> >

> >

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  • 2 months later...
Guest guest

Great letter--thanks so much.

Peacefully,

Jeff Sell

Hitt * * Sell

4309 Yoakum Blvd.

Suite 2000

Houston, TX 77006

www.HittSell.com

(fax)

JZSell@... (office)

(cell/v-mail)

jzsell@... (home)

(unknown)

HERE IS THE COPY OF THE LETTER I

SENT TO MY REPRESENTATIVE IN THE HOUSE.

I am a special educator for 12 years.

I have taught children with a wide range

of abilities and disabilities. One of

the most difficult obstacles special and

regular teachers face today is how to

gain the knowledge and support we need

to teach students with Autism. The number

is increasing dramatically, as you may

know and the schools are inundated with

young children needing extremely specific

skills. Your average teacher is in need

of support.

Some districts are hiring Autism Specialists

to help out but they will need funding.

HR 4728 will enable districts to support these

children families and teachers. If this does

not pass, it will send a very cold hearted

message to those committed to helping teach

children on this very difficult road to a life

worth living.

If IDEA is to remain under-funded,

conscience would dictate that help should come

from another source....the passage of HR 4728.

I will look for your vote on this and for any

additional support you may be able to give.

Thank you, sincerely.

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Guest guest

Dear ,

I strongly empathise with your emotions in your letter and would like to know

more about you.

You can find out more about me at http://hope-tlc.autistics.org.

Being from UK I am not familiar with what IDEA stands for - although I just read

some bits about it on the net. In principle it sounds good. How will that be put

into practice ...I do not know.

Take great care and good luck in your quest

Kind Regards

Florica

---------------------------------

Relive the FIFA World Cup goals with exclusive video highlights!

http://fifaworldcup.yahoo.com/fc/en

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  • 7 months later...

In a message dated 2/10/2003 1:23:52 PM Central Standard Time,

joeycmiller@... writes:

> I just heard today that my daughter's school & they will not evaluate

> her for Autism since she has already been diagnosed with a primary of

> epilepsy. I don't get this. Last summer they reevaluated her because

> she regressed so terribly and gave her the MR diagnosis. Her teacher

> said that she wouldn't get any additional services anyway even if

> they did evaluate her for Autism. She also admitted that Mallorie has

> many autistic characteristics but so do other conditions. Her neruo

> said she was autistic too.

> Is this worth getting into if they will not do anything else to help

> her? She gets some speech, ot, pt and music therapy at school. My son

> has just been diagnosed with Autism and will be starting next month

> when he turns 3. He will probably get some in home therapy but I

> don't know yet, we are waiting to have an ARD to request OT, autism

> evaluation, etc...... Why aren't there any services or organizations

> in place to help children like mine? We don't qualify for anything

> because we are middle class. Any suggestions or do we just go on

> alone and as one person do what I can?

>

> Thanks,

>

>

HI ,

There is help these folks can whip out answers like crazy.

I am experiencing the exact same thing with Angel except I am very poor.

Tammy

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  • 2 weeks later...

Welcome Amy! Wow! It is great to hear from someone who has actually entered

public school AFTER receiving their certification in ABA. That is usually

the point where most LEAVE public schools to go into private practice. Glad

you have decided to work in public school and join this list!

We are glad you are here!

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In a message dated 2/19/2003 1:45:28 PM Central Standard Time,

amykj@... writes:

> Hello Fellow Lister's,

> I am new on this list and I just wanted to introduce myself to everyone.

> My name is Amy . I am living in Austin, Texas. I am a certified

> Associate Behavior Analyst (BCaBA) and a Assistant Speech Pathologist

> (SLP-A). I am currently working at Round Rock ISD as a speech and behavior

>

> therapist. I am also consulting with some in home programs both privately

> and through the school district. I have been working with autistic

> children

> for seven and a half years and I worked in the Horizon program at Capitol

> School of Austin for two years before I accepted this position at RRISD.

> At

> Horizon, we were mentored by Kelle Wood BCBA, an associate of Dr. Vince

> Carbone, and we also had the wonderful experience of working directly with

> Dr. Carbone during the school year. I have also attended Dr. Carbone's

> level one and three workshops.

> I love these kids and really enjoy working with them!

> Thanks for letting me introduce myself and I am excited to be a part of

> your list.

>

> Thanks again,

> Amy K.

You sound awesome I wish that I were rich and could just hire you in my home

lol for

my child lol. I need behavioral management for my child for autism she gets

speech therapy she is blind also :)

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Amy:

Bless your heart--we are excited to have you!!!!!!!!!

Peacefully,

Jeff Sell

Autism Society of America--1st Vice President

Chairman--ASA's Gov't Relations Committee

www.autism-society.org

(Houston Office)

(cell/v-mail)

www.HittSell.com

JZSell@...

(unknown)

Hello Fellow Lister's,

I am new on this list and I just wanted to introduce myself to everyone.

My name is Amy . I am living in Austin, Texas. I am a certified

Associate Behavior Analyst (BCaBA) and a Assistant Speech Pathologist

(SLP-A). I am currently working at Round Rock ISD as a speech and behavior

therapist. I am also consulting with some in home programs both privately

and through the school district. I have been working with autistic children

for seven and a half years and I worked in the Horizon program at Capitol

School of Austin for two years before I accepted this position at RRISD. At

Horizon, we were mentored by Kelle Wood BCBA, an associate of Dr. Vince

Carbone, and we also had the wonderful experience of working directly with

Dr. Carbone during the school year. I have also attended Dr. Carbone's

level one and three workshops.

I love these kids and really enjoy working with them!

Thanks for letting me introduce myself and I am excited to be a part of

your list.

Thanks again,

Amy K.

_________________________________________________________________

The new MSN 8: smart spam protection and 2 months FREE*

http://join.msn.com/?page=features/junkmail

<http://join.msn.com/?page=features/junkmail>

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In a message dated 2/20/2003 10:59:54 AM Central Standard Time,

purecntry@... writes:

>

> Your local ESC should have a low vision specialist. Ours in Lubbock did.

> Tonya

>

oh yes she gets lots of help for her blindness. She has a vision service

teacher a vision service aid and then lots of drs as well. She is totally

blind she has had 9 eye surgeries.

Tammy

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You sound awesome I wish that I were rich and could just hire you in my home

lol for my child lol. I need behavioral management for my child for autism

she gets speech therapy she is blind also :)

Your local ESC should have a low vision specialist. Ours in Lubbock did.

Tonya

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Welcome! We look forward to your input.

Tonya Hettler

West Texas

In a message dated 2/19/2003 1:45:28 PM Central Standard Time,

amykj@... writes:

> Hello Fellow Lister's,

> I am new on this list and I just wanted to introduce myself to everyone.

> My name is Amy . I am living in Austin, Texas. I am a certified

> Associate Behavior Analyst (BCaBA) and a Assistant Speech Pathologist

> (SLP-A). I am currently working at Round Rock ISD as a speech and

behavior

>

> therapist. I am also consulting with some in home programs both privately

> and through the school district. I have been working with autistic

> children

> for seven and a half years and I worked in the Horizon program at Capitol

> School of Austin for two years before I accepted this position at RRISD.

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