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Olivia's almost done pre-school and will be going to Kindergarten

in the fall but we're having a bit of a problem with the school she

goes to now. It's for both " regular " and " special needs " kids,

specializing in special needs and runs classes from toddler (12mths)

to Kindergarten. She's been going there for 2 years now and the

plan up until Thursday was to place her there for kindergarten as

well. We then found out that a little boy in her class now will

also be in the Kindergarten class, he has a severe speech delay and

is not understandable at all 98% of the time. He gets very

frustrated and will take it out physically and spends a lot of time

in time out. He's a good boy other than that and he gets along

great with Olivia (they're cute together as he's just over 55lbs!!!)

I just want to clarify that I have nothing against speech delays

or anything like that ( had horrible speech until she was 6)

but the problem is that his mom is the Kindergarten teacher. I'm

not sure why they're allowing this but on the other hand I know that

he really needs this program while Olivia really doesn't. Other

than her size we have no doubts that she would flourish in a reg.

kindergarten setting. She's tested out of OT --> 50%ile, still

needs PT --> 8%ile, but her speech and cognitave (sp) tested at a

whopping 95%ile for 4-5 yr olds.

We've already contacted the public school here and since she

alread has PUF funding we don't have to re-apply, it will go with

her to any school that she attends. We'll have a one time OT

consult at the school to tour the school and classroom to see what

Olivia will need for independance (size appropriate

desk/table/chair, lowered coat hook, stools at the fountain and

sink, etc, etc)

I'm not sure if I'm making a mountain out of a mole hill or what

but it leaves a heavy feeling in my stomach when I think about it!!

Any input from teachers here (Jodi Z. maybe) or any one else would

be great!!

Leah, mom to Ash 9 and Olivia 4.5, RSS, OI, 19lbs!, 33 " , lactulose,

senokot, zantac, cyproheptadine (periactin)

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Just a moms point of view here.

I would put Olivia in a regular kindergarten class. From what you wrote I do

not see a need for her to be in that class. The speech impaired child will be

taking up alot of the teachers time and Olivia will not be getting what she

needs.

In Lindsey class this year. There is a child the size of a two year,and weight

less. and its just not an issue.. MY child gets the questions because she is

speech impaired(verbal and oral apraxia),fine motor problems,devopmentally

delayed and can be a defiant! In kindergarten she was not understood AT all.,and

she acted out.She's repeated K twice and once again she's in another K with 3

special needs first graders, my child being one of the first graders. The

special needs children are accepted completely.

If Olivia's not cognitively impaired,I would surely put her in a regular

kindergarten class in a regular school.It sounds like her needs will be met with

the adaptations she will receive.

Lindsey is going to a self contained class in the fall,she will be a second

grader.

Good luck,Go with your gut. Moms know best!

Jennie

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Leah

What does the special setting offer that you feel the regular kindergarten

placement would not? I think that would make the difference.

I can see your concerns. My son was always in the " main stream " with the OT

assessments for physcial suitability. One thing to keep in mind, from

experience!, have the OT check any doors that Olivia may be expected to open

and close regularly. One year Adam had a heavy fire door that he had to open

and close to go to the washroom. I didn't want him singled out by having to

take a " buddy " everytime he went out. The OT felt it needed automatic door

openers (she said Adam was jumping down off the last step, running full

speed for the door, using that momentum to open the door and then wail

himself through it.....she said one kid, just one, needs to get in his way

and he'd be " Adam sandwich " as she put it.)

Meanwhile the request went in, but the school board kept delaying until they

had funds. Ended up I requested he be allowed to use the intermediate stair

way (that had the automatic doors already). Just something to consider.

My gut feeling and the recommendation I make as a special ed. teacher is to

mainstream as much as possible. Olivia is very bright from the scores you

mentioned and if the other kids are struggling academically and the teacher

needs to remediate or go at a slower pace for the majority of the kids,

Olivia is going to be bored.

Debby

School Decision - long

>

>

> Olivia's almost done pre-school and will be going to Kindergarten

> in the fall but we're having a bit of a problem with the school she

> goes to now. It's for both " regular " and " special needs " kids,

> specializing in special needs and runs classes from toddler (12mths)

> to Kindergarten. She's been going there for 2 years now and the

> plan up until Thursday was to place her there for kindergarten as

> well. We then found out that a little boy in her class now will

> also be in the Kindergarten class, he has a severe speech delay and

> is not understandable at all 98% of the time. He gets very

> frustrated and will take it out physically and spends a lot of time

> in time out. He's a good boy other than that and he gets along

> great with Olivia (they're cute together as he's just over 55lbs!!!)

>

>

> I just want to clarify that I have nothing against speech delays

> or anything like that ( had horrible speech until she was 6)

> but the problem is that his mom is the Kindergarten teacher. I'm

> not sure why they're allowing this but on the other hand I know that

> he really needs this program while Olivia really doesn't. Other

> than her size we have no doubts that she would flourish in a reg.

> kindergarten setting. She's tested out of OT --> 50%ile, still

> needs PT --> 8%ile, but her speech and cognitave (sp) tested at a

> whopping 95%ile for 4-5 yr olds.

>

>

> We've already contacted the public school here and since she

> alread has PUF funding we don't have to re-apply, it will go with

> her to any school that she attends. We'll have a one time OT

> consult at the school to tour the school and classroom to see what

> Olivia will need for independance (size appropriate

> desk/table/chair, lowered coat hook, stools at the fountain and

> sink, etc, etc)

>

> I'm not sure if I'm making a mountain out of a mole hill or what

> but it leaves a heavy feeling in my stomach when I think about it!!

> Any input from teachers here (Jodi Z. maybe) or any one else would

> be great!!

>

> Leah, mom to Ash 9 and Olivia 4.5, RSS, OI, 19lbs!, 33 " , lactulose,

> senokot, zantac, cyproheptadine (periactin)

>

>

>

>

>

>

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Leah,

Even if Olivia were not facing going to school with the boy with the

behavior problems (forget the speech, that is the least of it), I

would recommend that you place her in a mainstreamed Kindergarten

class. It sounds like she is ready for it and, unless she has any

special learning concerns - which she does not from what you have

written - a mainstreamed class is best for her.

I am surprised that the boy is allowed to be in the same class as

his mom. That is really not professional or ethical, in my

opinion. But that is not your problem to deal with.

I hope that Olivia has a great year in kindergarten. It sure sounds

like she is ready!

Jodi Z.

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Leah,

I suggest you try the regular kindergarten class for Olivia. As far as the

adaptation to the

desk, chair, etc. - that is easy to get done. However, after kindergarten you

may need to

stay on top of the school to keep providing accommodations. I am not sure what

your

school system is like as far as getting services, but in many school systems it

can be

tricky to get what you want/need. I am an ESE teacher for severely emotionally

disturbed

students. When my son started kindergarten, he was " medically fragile " and the

health

department for the school system suggested that he go to a school where there

was a

nurse. At the time, the only schools in my district which had nurses were

centers, and

the ones with medically fragile students were mentally handicapped centers.

Obviously,

this did not fit the bill for , as he has normal intelligence.

With a lot of struggling, the school board provided a nurse at his school to

take care of

his g-tube feedings and other medical needs. He had a nurse in some capacity

until the

middle of 3rd grade. He is just finishing 4th grade now, and has always been in

regular

classes. He also has had a unique aide since kindergarten, and I would suggest

you look

into this for Olivia. They may call it something else in your school system,

but basically

this is a paraprofessional or teacher's aide who can assist Olivia with her

needs that are

different from the other students in the class. This person can be assigned to

her full-

time or only during activities where she is needed. I don't want to scare you,

but

depending on the level of Olivia's needs, you may go through some struggles to

get what

is best for her. This has been somethng I have dealt with for many years with

my son,

and for most of his schooling, I was an ESE Specialist, who facilitates ESE

meetings and

places referrals for testing. The one thing I still struggle with is that I am

sure my son

has a learning disability, and his school refuses to test him for this. One

would think

that because of my position with the school sysytem that they would humor me

even if

they felt I was wrong (though I am sure that I am not), but it still hasn't

happened yet. I

will admit though that they are providing the services he needs in relation to

this, but I

would like the testing to be done to hopefully get some answers on his

processing

problems.

In any event, I wish you luck in your decision & good luck to to Olivia for

kindergarten!

Kim C.

>

>

> Olivia's almost done pre-school and will be going to Kindergarten

> in the fall but we're having a bit of a problem with the school she

> goes to now. It's for both " regular " and " special needs " kids,

> specializing in special needs and runs classes from toddler (12mths)

> to Kindergarten. She's been going there for 2 years now and the

> plan up until Thursday was to place her there for kindergarten as

> well. We then found out that a little boy in her class now will

> also be in the Kindergarten class, he has a severe speech delay and

> is not understandable at all 98% of the time. He gets very

> frustrated and will take it out physically and spends a lot of time

> in time out. He's a good boy other than that and he gets along

> great with Olivia (they're cute together as he's just over 55lbs!!!)

>

>

> I just want to clarify that I have nothing against speech delays

> or anything like that ( had horrible speech until she was 6)

> but the problem is that his mom is the Kindergarten teacher. I'm

> not sure why they're allowing this but on the other hand I know that

> he really needs this program while Olivia really doesn't. Other

> than her size we have no doubts that she would flourish in a reg.

> kindergarten setting. She's tested out of OT --> 50%ile, still

> needs PT --> 8%ile, but her speech and cognitave (sp) tested at a

> whopping 95%ile for 4-5 yr olds.

>

>

> We've already contacted the public school here and since she

> alread has PUF funding we don't have to re-apply, it will go with

> her to any school that she attends. We'll have a one time OT

> consult at the school to tour the school and classroom to see what

> Olivia will need for independance (size appropriate

> desk/table/chair, lowered coat hook, stools at the fountain and

> sink, etc, etc)

>

> I'm not sure if I'm making a mountain out of a mole hill or what

> but it leaves a heavy feeling in my stomach when I think about it!!

> Any input from teachers here (Jodi Z. maybe) or any one else would

> be great!!

>

> Leah, mom to Ash 9 and Olivia 4.5, RSS, OI, 19lbs!, 33 " , lactulose,

> senokot, zantac, cyproheptadine (periactin)

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Kim,

What type of Problems do you believe your son has? I ask only because we

have been through it to. Jed my 11 year old I KNOW has a LD and the school

just says in their own way that he is just stupid.. Well we had him tested

and he has CAPD but of course they will not accept that diagnose, becuae in

Orange county it is not considered a disability (but 2 towns over in

seminloe conty) it is!!!!

So I have BTDT many times and know what you are going through.....

But you would think that since you are an ESE teacher they would listen to

you....

Mom to Liam (3 1/2 years old 34 3/4 " 27 lbs

SGA, Hypothyriod, Epilepsy.) Started GHT 5/18/04

and Jed (11 years old)

SW Orlando FL

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,

I cannot believe that CAPD is not considered a learning disability!

Your son should have accommodations, including a (oh, damn, I forgot

the name of it and I used to use one in my classroom for this

purpose!!!!!) - it's like a personal microphone and hearing system.

The teacher wears the microphone and your son wears headphones so

that the teacher's voice is louder and clearer for him. It also

blocks out background noise. I can't believe I can't think of the

name! I so support the use of these in the classroom. I'll think

of it eventually.

What has probably happened is that they tested your son and he is

within the average range, even if it is low average. Because of the

new trend of trying to keep kids in the mainstream and not

individualize too much, they are taking the theory that someone has

to be in the middle or low range, and your son is one of them.

Forget that you see more potential. Forget that you KNOW if he had

some specific things done to make things easier for him he would do

much better. It is so sad to see. It is frustrating for me, as a

special ed teacher. I try to hard to individualize where I can, but

keeping the kids working together at the same time. It is doable,

but difficult and the regular classroom teacher is not trained to do

this and most of the time just does not have the resources to do

it.

We have been through this with our daughter. She was in the high

end of average, according to the private testing we had done, but

the school would not do anything to help address her diagnosed

learning disability. They point blank told us that theory I told

you in the above. She struggled through school and it was sometimes

frustrating for us all. She had the potential to be an A student,

but barely graduated with a 2.9 average.

Then Jenna went on to college. She was able to choose her own

courses and focus on what interested her. I am happy to say that

she just completed her freshman year with a 3.8!!! I'm not bragging

here. I just want to let you know that you probably will have a

struggle, but do not give up. When he is able to focus on what

interests him, he will do better. You just have to help him through

and support him as best you can. Sometimes I hate our educational

system.

Jodi Z.

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Jodie,

Jed scored WAY Below on the CAPD tests... But the district does not consider

it a learning disability here... some districts do, ours does not....

When the school did their tests he came up with a low IQ.. So they basicly

told us in a round about way ( before we had him tested on our own for CAPD)

that he was just stupid. and couldn't be helped.... My hubby pointed out to

them, that if you look closely at his scores.. Where he did have help

(reading tutoring) the scores were higher... If he was turely stupid the

scores would not have changed with tutoring.. Therefore it shows an LD not a

lack of intellegiance... the GC just got up and left!!!!

L\ Mom to Liam (3 1/2 years old 34 3/4 " 27 lbs

SGA, Hypothyriod, Epilepsy.) Started GHT 5/18/04

and Jed (11 years old)

SW Orlando FL

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Can't you challenge this? Isn't there a supervisor of special

services that you can go to? This just does not seem right or

ethical.

Jodi Z.

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Dear Kim,

I don't know where you are, but one possible answer to the need for

comprehensive testing might be to go to a Shriner's Hospital. They

do the kind of testing that you need. And there is no cost to you.

They run strictly on donations and fundraising and patients do not

pay. I am not sure of the method to sign up or whatever and there

may be a wait of a few weeks to get in.

Conny, 's great-aunt

> >

> >

> > Olivia's almost done pre-school and will be going to

Kindergarten

> > in the fall but we're having a bit of a problem with the school

she

> > goes to now. It's for both " regular " and " special needs " kids,

> > specializing in special needs and runs classes from toddler

(12mths)

> > to Kindergarten. She's been going there for 2 years now and the

> > plan up until Thursday was to place her there for kindergarten as

> > well. We then found out that a little boy in her class now will

> > also be in the Kindergarten class, he has a severe speech delay

and

> > is not understandable at all 98% of the time. He gets very

> > frustrated and will take it out physically and spends a lot of

time

> > in time out. He's a good boy other than that and he gets along

> > great with Olivia (they're cute together as he's just over

55lbs!!!)

> >

> >

> > I just want to clarify that I have nothing against speech

delays

> > or anything like that ( had horrible speech until she was

6)

> > but the problem is that his mom is the Kindergarten teacher. I'm

> > not sure why they're allowing this but on the other hand I know

that

> > he really needs this program while Olivia really doesn't. Other

> > than her size we have no doubts that she would flourish in a reg.

> > kindergarten setting. She's tested out of OT --> 50%ile, still

> > needs PT --> 8%ile, but her speech and cognitave (sp) tested at a

> > whopping 95%ile for 4-5 yr olds.

> >

> >

> > We've already contacted the public school here and since she

> > alread has PUF funding we don't have to re-apply, it will go with

> > her to any school that she attends. We'll have a one time OT

> > consult at the school to tour the school and classroom to see

what

> > Olivia will need for independance (size appropriate

> > desk/table/chair, lowered coat hook, stools at the fountain and

> > sink, etc, etc)

> >

> > I'm not sure if I'm making a mountain out of a mole hill or

what

> > but it leaves a heavy feeling in my stomach when I think about

it!!

> > Any input from teachers here (Jodi Z. maybe) or any one else

would

> > be great!!

> >

> > Leah, mom to Ash 9 and Olivia 4.5, RSS, OI, 19lbs!, 33 " ,

lactulose,

> > senokot, zantac, cyproheptadine (periactin)

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,

As far as the possible LD goes, I think he definitely has a processing problem,

though

maybe not the same as your son with CAPD. Every child requires repetition to

learn

things, but I swear with , you can reapeat the same type of math problem

100

times in a row, and he acts like he has never seen that type of math problem

before each

time it it presented. His reading comprehension is also very poor, though his

decoding

& spelling skills are high. When I first asked about getting him tested, he was

a 1st

grader. The ESE Specialist at his school told me he wasn't 2 years below grade

level, so

he couldn't have a learning disability. I told her that was not the definition

of a learning

diability, and we argued back and forth for a long time. I was also an ESE

Specialist at

the time, but with not as much experience as the one at his school. She didn't

like to be

told she was wrong in front of a large group of people, especially by someone

her junior.

After several requests, they finally brought a psychologist in to speak with me,

and she

said his test scores weren't reflective of needing an evaluation. I think this

was after a

prediscussi9on though with the ESE Specialist at his school which did not

include me. At

the time he had a big discrepancy between his math and reading scores on the

SAT, and

his classroom grades were marginal. I have had other issues in the past due to

his

medical needs, and I really didn't want to rock the boat, so to speak, as her

boss was

also my boss, which put me in a small predicament. Now I am a

reading/curriculum

specialist for ESE students, and his school still won't listen to me. I do make

sure that

they put it in writing though that I had a concern each time we meet. That way,

if

anything surfaces later, I will be able to catch the school district in their

mistake. He has

one more year of elementary school, and then I will be dealing with another ESE

Specialist for middle school, so we will see how that goes....

I am also shocked to find out that Jed is not getting the services he needs.

They might

not consider that a disability so to speak, but he should at least fit into the

category

other health impaired (this is the category that ADHD kids fit into). That way,

he could

still get services, and the school would have to consider his doctor's notes to

make the

eligibility consideration. You may want to check more into this.

Kim

> Kim,

>

> What type of Problems do you believe your son has? I ask only because we

> have been through it to. Jed my 11 year old I KNOW has a LD and the school

> just says in their own way that he is just stupid.. Well we had him tested

> and he has CAPD but of course they will not accept that diagnose, becuae in

> Orange county it is not considered a disability (but 2 towns over in

> seminloe conty) it is!!!!

>

> So I have BTDT many times and know what you are going through.....

>

> But you would think that since you are an ESE teacher they would listen to

> you....

>

> Mom to Liam (3 1/2 years old 34 3/4 " 27 lbs

> SGA, Hypothyriod, Epilepsy.) Started GHT 5/18/04

> and Jed (11 years old)

> SW Orlando FL

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Poor , That is exactly how learning Algebra felt to me. I

used to tell the teacher that I was mathematically retarded. He

would teach me how the work the problems on Monday and I would be

humming along and by Wednesday, I had no clue what was going on

again! It was as though I had never seen them before. Conny,

's great-aunt

> > Kim,

> >

> > What type of Problems do you believe your son has? I ask only

because we

> > have been through it to. Jed my 11 year old I KNOW has a LD and

the school

> > just says in their own way that he is just stupid.. Well we had

him tested

> > and he has CAPD but of course they will not accept that diagnose,

becuae in

> > Orange county it is not considered a disability (but 2 towns over

in

> > seminloe conty) it is!!!!

> >

> > So I have BTDT many times and know what you are going through.....

> >

> > But you would think that since you are an ESE teacher they would

listen to

> > you....

> >

> > Mom to Liam (3 1/2 years old 34 3/4 " 27 lbs

> > SGA, Hypothyriod, Epilepsy.) Started GHT 5/18/04

> > and Jed (11 years old)

> > SW Orlando FL

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<

>

We did and it dosen't seem to help anyway.... they still want their own

tests....it may just push them to test him them selves....

Mom to Liam (3 1/2 years old 34 3/4 " 27 lbs

SGA, Hypothyriod, Epilepsy.) Started GHT 5/18/04

and Jed (11 years old)

SW Orlando FL

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