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I've used the book "We'll Paint the Octopus Red" by Stuve-Bodeen in both a kindergarten and first grade classroom. It is very simple and also provides a question and answer book about DS at the end. Books are great tools to generate questions, which you can then answer in nontechnical terms, and not make it feel like a lecture.

Janice Troy

Down Syndrome Association of San

-----Original Message-----From: Down Syndrome Treatment [mailto:Down Syndrome Treatment ]On Behalf Of GTCand4@...Sent: Wednesday, July 05, 2006 9:11 AMdownsyndrome Cc: down_syndrome ; Down Syndrome Treatment Subject: Dual diagnosis school speech

Hi All,

I have a question for those of you that have a child with a dual diagnosis or even those that don't but can also help.

I am trying to get together things I have to do before school starts in the fall (yes, like I don't have enough to do! :-) and one thing I am trying to do is get a classroom "speech" together.

Now, my problem is ... my daughter (5) has DS and diabetes and I am trying to write a letter to the parents of her classmates as well as get my thoughts written down for a "talk/Q & A" with the children of her class.

How can I include both diagnosis without sounding overwhelming to the children and parents? Since DS and diabetes is kinda involved I am having a hard time getting my point to them and not sounding to clinical.

Have any of you with dual diagnosis ever done this and if so, please help. :-)

I am hoping to get something really awesome written so I can just update as needed throughout her schooling days.

I have a diabetes book geared towards the kindergarten age that I thought I'd read and I am trying to find the right DS book too.

in VA

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When my son was in kindergarten, I used the " My Friend Isabelle " book, read it

to the class, talked about differences and how we are all different but more

alike, than different, etc. Then after the talk, (my son) presented the

copy of the book to his teacher (in front of the class) to keep in the classroom

for her to use that year and in future years.

Hope that helps -

DSANI - Fort Wayne, IN - mom to , 8 (almost 9-yikes!!) Ds and Hannah, 7

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

From: GTCand4@...

Date: Wed Jul 05 09:10:46 CDT 2006

downsyndrome

Cc: down_syndrome , Down Syndrome Treatment

Subject: Dual diagnosis school speech

Hi All, I have a question for those of you that have a child with a dual

diagnosis or even those that don't but can also help. I am trying to get

together things I have to do before school starts in the fall (yes, like I don't

have enough to do! :-) and one thing I am trying to do is get a classroom

" speech " together.Now, my problem is ... my daughter (5) has DS and diabetes and

I am trying to write a letter to the parents of her classmates as well as get my

thoughts written down for a " talk/Q & A " with the children of her class.  How

can I include both diagnosis without sounding overwhelming to the children and

parents?   Since DS and diabetes is kinda involved I am having a hard time

getting my point to them and not sounding to clinical. Have any of you with dual

diagnosis ever done this and if so, please help. :-) I am hoping to get

something really awesome written so I can just update as needed throughout her

schooling days. I have a diabetes book geared towards the kindergarten age that

I thought I'd read and I am trying to find the right DS book too.  in VA

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When I have talked with Faith's class, both K and 1st, the children's questions are pretty basic. Like "Why does she talk different?" I used an example of talking with a mouthful of licorice or marshmallows, they got the idea. "Is she REALLY 8?" Yes, she's just small. And how about "Where was she born?" After I explained DS a couple of times, probably over their heads, a boy asked "But what IS Down Syndrome?"

It will probably be even harder to explain "what" diabetes is, but at least there is the physical (injections, I assume) to show.

I don't really like the children's books I've found, they all seem to have something objectionable to me. So I used a photo album of Faith as a baby, talked about how she was born early, then about her heart surgery. How it takes her longer to do things, like walk, talk, learn to read, and do math. Let them know sometimes she wants help, but sometimes she wants to do it herself, just like they do. I tried to reference how much she is like them, they know the differences already.

Good luck!

ette

mom to Faith (8)DS

-------------- Original message from GTCand4@...: --------------

Hi All,

I have a question for those of you that have a child with a dual diagnosis or even those that don't but can also help.

I am trying to get together things I have to do before school starts in the fall (yes, like I don't have enough to do! :-) and one thing I am trying to do is get a classroom "speech" together.

Now, my problem is ... my daughter (5) has DS and diabetes and I am trying to write a letter to the parents of her classmates as well as get my thoughts written down for a "talk/Q & A" with the children of her class.

How can I include both diagnosis without sounding overwhelming to the children and parents? Since DS and diabetes is kinda involved I am having a hard time getting my point to them and not sounding to clinical.

Have any of you with dual diagnosis ever done this and if so, please help. :-)

I am hoping to get something really awesome written so I can just update as needed throughout her schooling days.

I have a diabetes book geared towards the kindergarten age that I thought I'd read and I am trying to find the right DS book too.

in VA

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Have you seen the book “Pieces of Me” ?

http://piecesofme.741.com/index.html

kathyR

From: Down Syndrome Treatment [mailto:Down Syndrome Treatment ] On Behalf Of GTCand4@...

Sent: Wednesday, July 05, 2006

10:11 AM

downsyndrome

Cc: down_syndrome ;

Down Syndrome Treatment

Subject:

Dual diagnosis school speech

Hi All,

I have a question for those of you that

have a child with a dual diagnosis or even those that don't but can also help.

I am trying to get together things I have

to do before school starts in the fall (yes, like I don't have enough to do!

:-) and one thing I am trying to do is get a classroom " speech "

together.

Now, my problem is ... my daughter

(5) has DS and diabetes and I am trying to write a letter to the

parents of her classmates as well as get my thoughts written down for a

" talk/Q & A " with the children of her class.

How can I include both diagnosis without

sounding overwhelming to the children and parents? Since DS

and diabetes is kinda involved I am having a hard time getting my point to them

and not sounding to clinical.

Have any of you with dual diagnosis ever

done this and if so, please help. :-)

I am hoping to get something really

awesome written so I can just update as needed throughout her schooling days.

I have a diabetes book geared towards the

kindergarten age that I thought I'd read and I am trying to find the right DS

book too.

in VA

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Wow, great book and great sites in the links!

Thanks for posting,

Kathy

RE: Dual diagnosis school speech

Have you seen the book “Pieces of Me” ?

http://piecesofme.741.com/index.html

kathyR

From: Down Syndrome Treatment [mailto:Down Syndrome Treatment ] On Behalf Of GTCand4@...Sent: Wednesday, July 05, 2006 10:11 AMdownsyndrome Cc: down_syndrome ; Down Syndrome Treatment Subject: Dual diagnosis school speech

Hi All,

I have a question for those of you that have a child with a dual diagnosis or even those that don't but can also help.

I am trying to get together things I have to do before school starts in the fall (yes, like I don't have enough to do! :-) and one thing I am trying to do is get a classroom "speech" together.

Now, my problem is ... my daughter (5) has DS and diabetes and I am trying to write a letter to the parents of her classmates as well as get my thoughts written down for a "talk/Q & A" with the children of her class.

How can I include both diagnosis without sounding overwhelming to the children and parents? Since DS and diabetes is kinda involved I am having a hard time getting my point to them and not sounding to clinical.

Have any of you with dual diagnosis ever done this and if so, please help. :-)

I am hoping to get something really awesome written so I can just update as needed throughout her schooling days.

I have a diabetes book geared towards the kindergarten age that I thought I'd read and I am trying to find the right DS book too.

in VA

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This was so cool! We laughed at the pictures because Evan has those

same expressions on his face a lot!

Priscilla K

--- Kathy Ratkiewicz <Kathy_R@...> wrote:

> Have you seen the book " Pieces of Me " ?

>

> http://piecesofme.741.com/index.html

>

>

>

> kathyR

>

Priscilla Kendrick, married 28 years to Darrel and parents of 9 kids including

Evan, 10, born with Down Syndrome and Spina Bifida

" My strength is made perfect in weakness. "

" My grace is sufficient. " II Corinthians 12:9 KJV

__________________________________________________

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I thought about all this last year when entered kdgr and I decided to do 'nothing'. ;-) Well ,I did loan some of my books on DS to the teacher when she did her unit on differences. Nothing earth shattering, just the ABC book featuring kids with DS, Paint the Octupus Red, and My Brother has DS. She does the same unit each year that covers everything- glasses, deafness, skin color, general disability etc, so my books fit right in and they read them with out much reference to other then the same kinds they made about the different color of people's eyes. I opted out of the speech and bringing a lot of attention to . I wasn't really sure if it 'worked' or not, other then the fact that the school year went really well and no one seemed to think much about her being there... as in- no one questioned her being there. Towards the end of the year on the way home from a

field trip, one of the other moms who spent a lot of time in the room told me at the beginning of the year her dd came home talking about all the time. All this mom knew was couldn't talk as well as the other kids, but it was 'no big deal' to her dd. uses sign language' which kids seem to find fun and enjoy picking it up. The mom said her dd had no idea about DS, or what it meant, or even that there was such an animal. ;-) Therefore, she treated the same as she would any other kid who didn't talk so well, that really seemed to be the most interesting thing about her with the other kids. This mom was shocked ( her words ) when she did come to the class room and found out toad had DS. The reason she was shocked??? Her cousin has DS and I guess he was quite the handfull and not very capable of things. She had lots of 'ideas' about what people with DS could and

could not do. She had no idea from her dd's descriptions that Chrisitne was anything other then deaf. She went on to tell me that had totally changed her mind about people with DS and what they CAN do given the chance and some kid friendly pushing in the right direction. So I was happy I hadn't made a big deal of the DS and just let everyone kind of find their way. was present at all the concerts, so anyone who came ,knew! I DID print and give them lots of things from these two sites as the need arose - http://disabilityisnatural.com/ http://www.normemma.com/index.htm I was very blessed with the teacher who is my idea of a REAL teacher. She just loves teaching and kids in general. Has a real heart for people and just accepted was a kid like the rest and since she had never been around a person with DS,

she really had no idea what to expect and I kinda just let make her own impression on everyone. This is really one of my very favorite articles and one that I made sure everyone dealing with had read http://www.normemma.com/arhellbe.htm I think it really sets the 'tone' I like to use regarding her DS. Carol in IL

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I haven't done much in regards to addressing Mac's differences at school either. I've offered if they need me / want me to do something I will but haven't requested it myself. Actually, speech is the place where most kids notice Mac's differences the most, too. The question that has been asked frequently since he's been in K is "why can't he talk right?". Now they also see his stubborness sneaking in from time to time and I'll hear in the cafeteria or somewhere "Mac wasn 't very good today" or "Mac didn't want to do his math today" or "Mac is having a very good day"--so they know he's "different" but it's not a bad thing or a good thing--it just is and it's no big deal.

I do always put together a booklet for his new teacher each year...an "All About Me" booklet that has pictures of family and friends and of him doing just ordinary things. It also has a page of likes/dislikes, a few pages of "Ways to Help Me Learn" where I list various strategies that I know have worked with him in the past and a page of resources--books, articles, websites, list servs, etc... I usually also give each teacher a book that relates to Ds--in K and 1st I gave "Paint the Octopus Red" and last year "Be Kind to Eddie Lee"--not sure what to give this year, any suggestions? I also give the new teacher a pocket sign language book. I don't tell them to use them or even say anything...just a packet of goodies to use (or not use) as they choose to start the year.

Jill

Mom to Mac & Kit

Re: Dual diagnosis school speech

I thought about all this last year when entered kdgr and I decided to do 'nothing'. ;-) Well ,I did loan some of my books on DS to the teacher when she did her unit on differences. Nothing earth shattering, just the ABC book featuring kids with DS, Paint the Octupus Red, and My Brother has DS. She does the same unit each year that covers everything- glasses, deafness, skin color, general disability etc, so my books fit right in and they read them with out much reference to other then the same kinds they made about the different color of people's eyes.

I opted out of the speech and bringing a lot of attention to . I wasn't really sure if it 'worked' or not, other then the fact that the school year went really well and no one seemed to think much about her being there... as in- no one questioned her being there.

Towards the end of the year on the way h ome from a field trip, one of the other moms who spent a lot of time in the room told me at the beginning of the year her dd came home talking about all the time. All this mom knew was couldn't talk as well as the other kids, but it was 'no big deal' to her dd. uses sign language' which kids seem to find fun and enjoy picking it up. The mom said her dd had no idea about DS, or what it meant, or even that there was such an animal. ;-) Therefore, she treated the same as she would any other kid who didn't talk so well, that really seemed to be the most interesting thing about her with the other kids.

This mom was shocked ( her words ) when she did come to the class room and found out toad had DS. The reason she was shocked???

Her cousin has DS and I guess he was quite the handfull and not very capable of things. She had lots of 'ideas' about what people with DS could and could not do. She had no idea from her dd's descriptions that Chrisitne was anything other then deaf. She went on to tell me that had totally changed her mind about people with DS and what they CAN do given the chance and some kid friendly pushing in the right direction. So I was happy I hadn't made a big deal of the DS and just let everyone kind of find their way.

was present at all the concerts, so anyone who came ,knew!

I DID print and give them lots of things from these two sites as the need arose - http://disabilityisnatural.com/ http://www.normemma.com/index.htm

I was very blessed with the teacher who is my idea of a REAL teacher. She just loves teaching and kids in general. Has a real heart for people and just accepted was a kid like the rest and since she had never been around a person with DS, she really had no idea what to expect and I kinda just let make her own impression on everyone.

This is really one of my very favorite articles and one that I made sure everyone dealing with had read

http://www.normemma.com/arhellbe.htm

I think it really sets the 'tone' I like to use regarding her DS.

Carol in IL

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I have a bag of books that follows each year to the gen. ed class --

includes Teaching Reading, Teaching Math, Classroom Language, Sue People's book

on teaching kids w/ Ds and My Friend Isabelle, NDSS Inclusion booklet - this

year I will add the NDSS Everyone Counts program -- our group has given the same

bag (plus the Gross Motor and Fine Motor books) to all the elementary schools in

our 11 counties so my elementary school has 2 sets but I know that one is always

available to the teacher in 's classroom.

DSANI - Fort Wayne

mom to , 8, Ds and Hannah, 7

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

From: Jill <thrill@...>

Date: Tue Jul 11 12:46:26 CDT 2006

Down Syndrome Treatment

Subject: Re: Dual diagnosis school speech

I haven't done much in regards to addressing Mac's differences at school

either.  I've offered if they need me / want me to do something I will but

haven't requested it myself.   Actually, speech is the place where most kids

notice Mac's differences the most, too.  The question that has been asked

frequently since he's been in K is " why can't he talk right? " .  Now they also

see his stubborness sneaking in from time to time and I'll hear in the cafeteria

or somewhere " Mac wasn 't very good today " or " Mac didn't want to do his math

today " or " Mac is having a very good day " --so they know he's " different " but

it's not a bad thing or a good thing--it just is and it's no big deal.  I do

always put together a booklet for his new teacher each year...an " All About Me "

booklet that has pictures of family and friends and of him doing just ordinary

things.  It also has a page of likes/dislikes, a few pages of " Ways to Help Me

Learn " where I list various strategies that I know have worked with him in the

past and a page of resources--books, articles, websites, list servs, etc...  I

usually also give each teacher a book that relates to Ds--in K and 1st I gave

" Paint the Octopus Red " and last year " Be Kind to Eddie Lee " --not sure what to

give this year, any suggestions?  I also give the new teacher a pocket sign

language book.  I don't tell them to use them or even say anything...just a

packet of goodies to use (or not use) as they choose to start the year. JillMom

to Mac & Kit   Re: Dual diagnosis school speech

I thought about all this last year when entered kdgr and I decided

to do 'nothing'. ;-) Well ,I did loan some of my books on DS to the teacher

when she did her unit on differences. Nothing earth shattering, just the ABC

book featuring kids with DS, Paint the Octupus Red, and My Brother has DS. 

She does the same unit each year that covers everything- glasses, deafness,

skin color, general disability etc, so my books fit right in and they read

them with out much reference to other then the same kinds they made

about the different color of people's eyes.   I opted out of the speech

and bringing a lot of attention to . I wasn't really sure if it

'worked' or not, other then the fact that  the school year went really well

and no one seemed to think much about her being there... as in- no one

questioned her being there.   Towards the end of the year on the way h ome

from a field trip, one of the other moms who spent a lot of time in the room

told me at the beginning of the year her dd came home talking about

all the time. All this mom knew was couldn't talk as well as the

other kids, but it was 'no big deal' to her dd.  uses sign language'

which kids seem to find fun and enjoy picking it up. The mom said her dd  had

no idea about DS, or what it meant, or even that there was such an animal. ;-)

Therefore, she treated the same as she would any other kid who

didn't talk so well, that really seemed to be the most interesting thing about

her with the other kids.   This mom was shocked ( her words ) when she did

come to the class room and found out toad had DS.  The reason she was

shocked??? Her cousin has DS and I guess he was quite the handfull and not very

capable of things. She had lots of 'ideas' about what people with DS could and

could not do. She had no idea from her dd's descriptions that Chrisitne was

anything other then deaf. She went on to tell me that had totally

changed her mind about people with DS and what they CAN do given the chance

and some  kid friendly pushing in the right direction. So I was happy I hadn't

made a big deal of the DS and just let everyone kind of find their way.

was present at all the concerts, so anyone who came ,knew!   I DID

print and give them lots of things from these two sites as the need arose -

http://disabilityisnatural.com/ http://www.normemma.com/index.htm   I was very

blessed with the teacher who is my idea of a REAL teacher. She just loves

teaching and kids in general. Has a real heart for people and just accepted

was a kid like the rest and since she had never been around a person

with DS, she really had no idea what to expect and I kinda just let

make her own impression on everyone.   This is really one of my very favorite

articles and one that I made sure everyone dealing with had read

http://www.normemma.com/arhellbe.htm   I think it really sets the 'tone' I

like to use regarding her DS.   Carol in IL

Talk is cheap. Use Messenger to make PC-to-Phone calls. Great rates

starting at 1¢/min.

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--

Do you know if the NDSS Inclusion booklet is still in print and available? I also have given that every year--I was just going through my "stuff" and I only have two copies left. I heard there may be a new updated one, but haven't seen anything about that.

I also give the Sue People's book. One thing that disturbs me, not about the book, but about a presentation I went to this spring by Sue was that she made a statement, actually in her words she said she was quoting an NDSS study about inclusion and that the study showed that children with Ds learn academics best in 1:1/small group settings, not in large group settings--to me and to my son's teachers who went and are anti-inclusion this meant general ed classrooms are not an appropriate placement for him. My heart sunk when I heard and read that in her handouts and I was the one that really encouraged the special educators who work with my son to attend this conference and that was one of the main things they got from it--fuel for THEIR fire--her comments were quoted several times in his MFE and in his IEP. I was so disappointed. I did find the "study" and in reality it is not a study at all, but a survey of a limited number of people and their opinions about inclusion. It was NOT a study that really looked at inclusion or how children learn--probably most any child (disability or not) learns best 1:1 or in a small group setting, but typical classrooms (where I want my son to be) are not usually considered small group. This was just a vent I felt like sharing when you reminded me of the People's book--which I do think is excellent.

Jill

Mom to Mac (8 yrs, 3rd grade, Ds) and Kit (almost 5, preschool, Ds)

Re: Dual diagnosis school speech I thought about all this last year when entered kdgr and I decided to do 'nothing'. ;-) Well ,I did loan some of my books on DS to the teacher when she did her unit on differences. Nothing earth shattering, just the ABC book featuring kids with DS, Paint the Octupus Red, and My Brother has DS. She does the same unit each year that covers everything- glasses, deafness, skin color, general disability etc, so my books fit right in and they read them with out much reference to other then the same kinds they made about the different color of people's eyes. I opted out of the speech and bringing a lot of attention to . I wasn't really sure if it 'worked' or not, other then the fact that the school year went really well and no one seemed to think much about her being there... as in- no one questioned her being there. Towards the end of the year on the way h ome from a field trip, one of the other moms who spent a lot of time in the room told me at the beginning of the year her dd came home talking about all the time. All this mom knew was couldn't talk as well as the other kids, but it was 'no big deal' to her dd. uses sign language' which kids seem to find fun and enjoy picking it up. The mom said her dd had no idea about DS, or what it meant, or even that there was such an animal. ;-) Therefore, she treated the same as she would any other kid who didn't talk so well, that really seemed to be the most interesting thing about her with the other kids. This mom was shocked ( her words ) when she did come to the class room and found out toad had DS. The reason she was shocked??? Her cousin has DS and I guess he was quite the handfull and not very capable of things. She had lots of 'ideas' about what people with DS could and could not do. She had no idea from her dd's descriptions that Chrisitne was anything other then deaf. She went on to tell me that had totally changed her mind about people with DS and what they CAN do given the chance and some kid friendly pushing in the right direction. So I was happy I hadn't made a big deal of the DS and just let everyone kind of find their way. was present at all the concerts, so anyone who came ,knew! I DID print and give them lots of things from these two sites as the need arose - http://disabilityisnatural.com/ http://www.normemma.com/index.htm I was very blessed with the teacher who is my idea of a REAL teacher. She just loves teaching and kids in general. Has a real heart for people and just accepted was a kid like the rest and since she had never been around a person with DS, she really had no idea what to expect and I kinda just let make her own impression on everyone. This is really one of my very favorite articles and one that I made sure everyone dealing with had read http://www.normemma.com/arhellbe.htm I think it really sets the 'tone' I like to use regarding her DS. Carol in IL Talk is cheap. Use Messenger to make PC-to-Phone calls. Great rates starting at 1¢/min.

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Jill --

I have not heard Sue say that but will listen for it the next time I talk to her

and I haven't sat in on a presentation for a couple of years -- she is actually

a member of our group and her son attends the same school district mine does. I

know she has been working on some new techniques to teach our kiddos but in our

last (lengthy) conversation she didn't mention this study.

Last I checked the NDSS Inclusion brochure was still available.

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

From: Jill <thrill@...>

Date: Tue Jul 11 20:38:38 CDT 2006

Down Syndrome Treatment

Subject: Re: Re: Dual diagnosis school speech

--  Do you know if the NDSS Inclusion booklet is still in print and

available?  I also have given that every year--I was just going through my

" stuff " and I only have two copies left.  I heard there may be a new  updated

one, but haven't seen anything about that.    I also give the Sue People's

book.  One thing that disturbs me, not about the book, but about a presentation

I went to this spring by Sue was that she made a statement, actually in her

words she said she was quoting an NDSS study about inclusion and that the study

showed that children with Ds learn academics best in 1:1/small group settings,

not in large group settings--to me and to my son's teachers who went and are

anti-inclusion this meant general ed classrooms are not  an appropriate

placement for him.  My heart sunk when I heard and read that in her handouts and

I was the one that really encouraged the special educators who work with my son

to attend this conference and that was one of the main things they got from

it--fuel for THEIR fire--her comments were quoted several times in his MFE and

in his IEP.  I was so disappointed.  I did find the " study " and in reality it is

not a study at all, but a survey of a limited number of people and their

opinions about inclusion.  It was NOT a study that really looked at inclusion or

how children learn--probably most any child (disability or not) learns best 1:1

or in a small group setting, but typical classrooms (where I want my son to be)

are not usually considered small group.  This was just a vent I felt like

sharing when you reminded me of the People's book--which I do think is

excellent. JillMom to Mac (8 yrs, 3rd grade, Ds) and Kit (almost 5, preschool,

Ds)  Re: Dual diagnosis school speech

I thought about all this last year when entered kdgr and I decided

to do 'nothing'. ;-) Well ,I did loan some of my books on DS to the teacher

when she did her unit on differences. Nothing earth shattering, just the ABC

book featuring kids with DS, Paint the Octupus Red, and My Brother has DS. 

She does the same unit each year that covers everything- glasses, deafness,

skin color, general disability etc, so my books fit right in and they read

them with out much reference to other then the same kinds they made

about the different color of people's eyes.   I opted out of the speech

and bringing a lot of attention to . I wasn't really sure if it

'worked' or not, other then the fact that  the school year went really well

and no one seemed to think much about her being there... as in- no one

questioned her being there.   Towards the end of the year on the way h ome

from a field trip, one of the other moms who spent a lot of time in the room

told me at the beginning of the year her dd came home talking about

all the time. All this mom knew was couldn't talk as well as the

other kids, but it was 'no big deal' to her dd.  uses sign language'

which kids seem to find fun and enjoy picking it up. The mom said her dd  had

no idea about DS, or what it meant, or even that there was such an animal. ;-)

Therefore, she treated the same as she would any other kid who

didn't talk so well, that really seemed to be the most interesting thing about

her with the other kids.   This mom was shocked ( her words ) when she did

come to the class room and found out toad had DS.  The reason she was

shocked??? Her cousin has DS and I guess he was quite the handfull and not

very capable of things. She had lots of 'ideas' about what people with DS

could and could not do. She had no idea from her dd's

descriptions that Chrisitne was anything other then deaf. She went on to tell

me that had totally changed her mind about people with DS and what

they CAN do given the chance and some  kid friendly pushing in the right

direction. So I was happy I hadn't made a big deal of the DS and just let

everyone kind of find their way. was present at all the concerts, so

anyone who came ,knew!   I DID print and give them lots of things from these

two sites as the need arose - http://disabilityisnatural.com/

http://www.normemma.com/index.htm   I was very blessed with the teacher who is

my idea of a REAL teacher. She just loves teaching and kids in general. Has a

real heart for people and just accepted was a kid like the rest and

since she had never been around a person with DS, she really had no idea what

to expect and I kinda just let make her own impression on everyone.

  This is really one of my very favorite articles and one that I made sure

everyone dealing with had read http://www.normemma.com/arhellbe.htm

  I think it really sets the 'tone' I like to use regarding her DS.   Carol in

IL

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I have loaned school the reading and math books as well. I love the People's book and wanted everyone to read it and some have. I spose they will be using it against us then too??? I know she says to keep everything plain in the room, but honestly, I don't think that works with at all. She seems to love lots of things to look at after a while, they blend into the background untill they are changed. As for one on one, I know it helps for things she needs extra help with, otherwise, the gen ed room with it's 'buzz' of learning going on, seems to be the best place for learning. I am so amazed at what she picks up in there. I have always tended to 'flood' with info and she seems to suck it all in. Just goes to show that all kids are different. Did you happen to find this study on line and if so do you still have the url for it? I have a

feeling I may be needing it. ;-) Carol in IL Jill <thrill@...> wrote: -- Do you know if the NDSS Inclusion booklet is still in print and available? I also have given that every year--I was just going through my "stuff" and I only have two copies left. I heard there may be a new updated one, but haven't seen anything about that. I also give the Sue People's book.

One thing that disturbs me, not about the book, but about a presentation I went to this spring by Sue was that she made a statement, actually in her words she said she was quoting an NDSS study about inclusion and that the study showed that children with Ds learn academics best in 1:1/small group settings, not in large group settings--to me and to my son's teachers who went and are anti-inclusion this meant general ed classrooms are not an appropriate placement for him. My heart sunk when I heard and read that in her handouts and I was the one that really encouraged the special educators who work with my son to attend this conference and that was one of the main things they got from it--fuel for THEIR fire--her comments were quoted several times in his MFE and in his IEP. I was so disappointed. I did find the "study" and in reality it is not a study at all, but a survey of a limited number of people and their opinions about

inclusion. It was NOT a study that really looked at inclusion or how children learn--probably most any child (disability or not) learns best 1:1 or in a small group setting, but typical classrooms (where I want my son to be) are not usually considered small group. This was just a vent I felt like sharing when you reminded me of the People's book--which I do think is excellent. Jill Mom to Mac (8 yrs, 3rd grade, Ds) and Kit (almost 5, preschool, Ds) Re: Dual diagnosis school speech I thought about all this last year when entered kdgr and I decided to do 'nothing'. ;-) Well ,I did loan some of my books on DS to the teacher when she did her unit on differences. Nothing earth shattering, just the ABC book featuring kids with DS, Paint the Octupus Red, and My Brother has DS. She does the same unit each year that covers everything- glasses, deafness, skin color, general disability etc, so my books fit right in and they read them with out much reference to other then the same kinds they made about the different color of people's eyes. I opted out of the speech and bringing a lot of attention to . I wasn't really sure if it 'worked' or not, other then the fact that the

school year went really well and no one seemed to think much about her being there... as in- no one questioned her being there. Towards the end of the year on the way h ome from a field trip, one of the other moms who spent a lot of time in the room told me at the beginning of the year her dd came home talking about all the time. All this mom knew was couldn't talk as well as the other kids, but it was 'no big deal' to her dd. uses sign language' which kids seem to find fun and enjoy picking it up. The mom said her dd had no idea about DS, or what it meant, or even that there was such an animal. ;-) Therefore, she treated the same as she would any other kid who didn't talk so well, that really seemed to be the most interesting thing about her with the other kids. This mom was shocked ( her words ) when she did come to the class room and found out toad had DS. The reason she was shocked???

Her cousin has DS and I guess he was quite the handfull and not very capable of things. She had lots of 'ideas' about what people with DS could and could not do. She had no idea from her dd's descriptions that Chrisitne was anything other then deaf. She went on to tell me that had totally changed her mind about people with DS and what they CAN do given the chance and some kid friendly pushing in the right direction. So I was happy I hadn't made a big deal of the DS and just let everyone kind of find their way. was present at all the concerts, so anyone who came ,knew! I DID print and give them lots of things from these two sites as the need arose - http://disabilityisnatural.com/ http://www.normemma.com/index.htm I was very blessed with the teacher who is my idea of a REAL teacher. She just loves teaching

and kids in general. Has a real heart for people and just accepted was a kid like the rest and since she had never been around a person with DS, she really had no idea what to expect and I kinda just let make her own impression on everyone. This is really one of my very favorite articles and one that I made sure everyone dealing with had read http://www.normemma.com/arhellbe.htm I think it really sets the 'tone' I like to use regarding her DS. Carol in IL Talk is cheap. Use Messenger to make PC-to-Phone calls. Great rates starting at 1¢/min.

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Yes, she had it on an overhead, in her handout and said it. I got the impression (from this presentation) that her son is not included for academics--at least not core academics like Language Arts and Math. I will look again for the "study" and forward it on so you know what I'm talking about. Several people have told me I should contact Sue and/or NDSS and let them know how this is being presented. I think it's okay to share it as long as she states that is is a SURVEY not a STUDY--there is a difference and, like I said, school personnel who are anti-inclusion are going to use this to their advantage as if it were a tried, true and tested study.

I went to a conference your group put on in either 2003 or 2004--it was wonderful!! Chock full of information and sessions in one day and very affordable. Are you guys planning anything else in the near or distant future?

Jill

Re: Dual diagnosis school speech I thought about all this last year when entered kdgr and I decided to do 'nothing'. ;-) Well ,I did loan some of my books on DS to the teacher when she did her unit on differences. Nothing earth shattering, just the ABC book featuring kids with DS, Paint the Octupus Red, and My Brother has DS. She does the same unit each year that covers everything- glasses, deafness, skin color, general disability etc, so my books fit right in and they read them with out much reference to other then the same kinds they made about the different color of people's eyes. I opted out of the speech and bringing a lot of attention to . I wasn't really sure if it 'worked' or not, other then the fact that the school year went really well and no one seemed to think much about her being there... as in- no one questioned her being there. Towards the end of the year on the way h ome from a field trip, one of the other moms who spent a lot of time in the room told me at the beginning of the year her dd came home talking about all the time. All this mom knew was couldn't talk as well as the other kids, but it was 'no big deal' to her dd. uses sign language' which kids seem to find fun and enjoy picking it up. The mom said her dd had no idea about DS, or what it meant, or even that there was such an animal. ;-) Therefore, she treated the same as she would any other kid who didn't talk so well, that really seemed to be the most interesting thing about her with the other kids. This mom was shocked ( her words ) when she did come to the class room and found out toad had DS. The reason she was shocked??? Her cousin has DS and I guess he was quite the handfull and not very capable of things. She had lots of 'ideas' about what people with DS could and could not do. She had no idea from her dd's descriptions that Chrisitne was anything other then deaf. She went on to tell me that had totally changed her mind about people with DS and what they CAN do given the chance and some kid friendly pushing in the right direction. So I was happy I hadn't made a big deal of the DS and just let everyone kind of find their way. was present at all the concerts, so anyone who came ,knew! I DID print and give them lots of things from these two sites as the need arose - http://disabilityisnatural.com/ http://www.normemma.com/index.htm I was very blessed with the teacher who is my idea of a REAL teacher. She just loves teaching and kids in general. Has a real heart for people and just accepted was a kid like the rest and since she had never been around a person with DS, she really had no idea what to expect and I kinda just let make her own impression on everyone. This is really one of my very favorite articles and one that I made sure everyone dealing with had read http://www.normemma.com/arhellbe.htm I think it really sets the 'tone' I like to use regarding her DS. Carol in IL Talk is cheap. Use Messenger to make PC-to-Phone calls. Great rates starting at 1¢/min.

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I, too, think the book is REALLY good. I was just surprised when she presented this "study" and seemed so anti-inclusion for academics. I heard her 3-4 years ago and didn't get that impression at all. I also agree small group is probably great for most any kid, but some kids (maybe many) with disabilities can also learn and benefit from whole class instruction--like , like Mac and others--and whole group/large group instruction is the norm in most schools.

I'm going to look for the study/survey and forward it on. It may have been on the Riverbend site.

Jill

Re: Dual diagnosis school speech I thought about all this last year when entered kdgr and I decided to do 'nothing'. ;-) Well ,I did loan some of my books on DS to the teacher when she did her unit on differences. Nothing earth shattering, just the ABC book featuring kids with DS, Paint the Octupus Red, and My Brother has DS. She does the same unit each year that covers everything- glasses, deafness, skin color, general disability etc, so my books fit right in and they read them with out much reference to other then the same kinds they made about the different color of people's eyes. I opted out of the speech and bringing a lot of attention to . I wasn't really sure if it 'worked' or not, other then the fact that the school year went really well and no one seemed to think much about her being there... as in- no one questioned her being there. Towards the end of the year on the way h ome from a field trip, one of the other moms who spent a lot of time in the room told me at the beginning of the year her dd came home talking about all the time. All this mom knew was couldn't talk as well as the other kids, but it was 'no big deal' to her dd. uses sign language' which kids seem to find fun and enjoy picking it up. The mom said her dd had no idea about DS, or what it meant, or even that there was such an animal. ;-) Therefore, she treated the same as she would any other kid who didn't talk so well, that really seemed to be the most interesting thing about her with the other kids. This mom was shocked ( her words ) when she did come to the class room and found out toad had DS. The reason she was shocked??? Her cousin has DS and I guess he was quite the handfull and not very capable of things. She had lots of 'ideas' about what people with DS could and could not do. She had no idea from her dd's descriptions that Chrisitne was anything other then deaf. She went on to tell me that had totally changed her mind about people with DS and what they CAN do given the chance and some kid friendly pushing in the right direction. So I was happy I hadn't made a big deal of the DS and just let everyone kind of find their way. was present at all the concerts, so anyone who came ,knew! I DID print and give them lots of things from these two sites as the need arose - http://disabilityisnatural.com/ http://www.normemma.com/index.htm I was very blessed with the teacher who is my idea of a REAL teacher. She just loves teaching and kids in general. Has a real heart for people and just accepted was a kid like the rest and since she had never been around a person with DS, she really had no idea what to expect and I kinda just let make her own impression on everyone. This is really one of my very favorite articles and one that I made sure everyone dealing with had read http://www.normemma.com/arhellbe.htm I think it really sets the 'tone' I like to use regarding her DS. Carol in IL Talk is cheap. Use Messenger to make PC-to-Phone calls. Great rates starting at 1¢/min.

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Do you get the books back each year? I've given the books to teachers but rarely gotten anything back unless I went and got it! I don't really mind because the information gets out more, but it does get expensive!

ette

--------- Re: Dual diagnosis school speech I thought about all this last year when entered kdgr and I decided to do 'nothing'. ;-) Well ,I did loan some of my books on DS to the teacher when she did her unit on differences. Nothing earth shattering, just the ABC book featuring kids with DS

, Paint the Octupus Red, and My Brother has DS. She does the same unit each year that covers everything- glasses, deafness, skin color, general disability etc, so my books fit right in and they read them with out much reference to other then the same kinds they made about the different color of people's eyes. I opted out of the speech and bringing a lot of attention to . I wasn't really sure if it 'worked' or not, other then the fact that the school year went really well and no one seemed to think much about her being there... as in- no one questioned her being there. Towards the end of the year on the way h ome from a field trip, one of the other moms who spent a lot of time in the room told me at the beginning of the year her dd came home talking about all the time. All this mom knew was couldn't talk as well as the other kids, but it was 'no big deal' to her dd. uses sign language' which kids seem to find fun and enjoy picking it up. The mom said her dd had no idea about DS, or what it meant, or even that there was such an animal. ;-) Therefore, she treated the same as she would any other kid who didn't talk so well, that really seemed to be the most interesting thing about her with the other kids. This mom was shocked ( her words ) when she did come to the class room and found out toad had DS. The reason she was shocked??? Her cousin has DS and I guess he was quite the handfull and not very capable of things. She had lots of 'ideas' about what people with DS could and could not do. She had no idea from her dd's descriptions that Chrisitne was anything other then deaf. She went on to tell me that had totally changed her mind about people with DS and what they CAN do given the chance and some kid friendly pushing in the right direction. So I was happy I hadn't made a big deal of the DS and just let everyone kind of find their way. was present at all the concerts, so anyone who came ,knew! I DID print and give them lots of things from these two sites as the need arose - http://disabilityisnatural.com/ http://www.normemma.com/index.htm I was very blessed with the teacher who is my idea of a REAL teacher. She just loves teaching and kids in general. Has a real heart for people and just accepted was a kid like the rest and since she had never been around a person with DS, she really had no idea what to expect and I kinda just let make her own impression on everyone. This is really one of my very favorite articles and one that I made sure everyone dealing with had read http://www.normemma.com/arhellbe.htm I think it really sets the 'tone' I like to use regarding her DS. Carol in IL Talk is cheap. Use Messenger to make PC-to-Phone calls. Great rates

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I believe this is the link to the study...I just did some searching and found two "quotes" from this "study" (and yes it is considered a study, altho I don't agree) in my handout from the presentation, so I think it is it. I didn't save it when I searched it out last time.

http://www.altonweb.com/cs/downsyndrome/index.htm?page=wolpert.html

Below are the remarks that Peoples shared during her workshop. Again, I wouldn't have a problem with this being reported if she would have given more background information, such as this was a study done via a questionnaire of a small number of parents and teachers (who returned their questionnaire) and their thoughts about inclusion.

Large groups and the whole class were reported not effective at all for students with Down syndrome.

individualized instruction and small groups being the most effective.

Re: Dual diagnosis school speech I thought about all this last year when entered kdgr and I decided to do 'nothing'. ;-) Well ,I did loan some of my books on DS to the teacher when she did her unit on differences. Nothing earth shattering, just the ABC book featuring kids with DS, Paint the Octupus Red, and My Brother has DS. She does the same unit each year that covers everything- glasses, deafness, skin color, general disability etc, so my books fit right in and they read them with out much reference to other then the same kinds they made about the different color of people's eyes. I opted out of the speech and bringing a lot of attention to . I wasn't really sure if it 'worked' or not, other then the fact that the school year went really well and no one seemed to think much about her being there... as in- no one questioned her being there. Towards the end of the year on the way h ome from a field trip, one of the other moms who spent a lot of time in the room told me at the beginning of the year her dd came home talking about all the time. All this mom knew was couldn't talk as well as the other kids, but it was 'no big deal' to her dd. uses sign language' which kids seem to find fun and enjoy picking it up. The mom said her dd had no idea about DS, or what it meant, or even that there was such an animal. ;-) Therefore, she treated the same as she would any other kid who didn't talk so well, that really seemed to be the most interesting thing about her with the other kids. This mom was shocked ( her words ) when she did come to the class room and found out toad had DS. The reason she was shocked??? Her cousin has DS and I guess he was quite the handfull and not very capable of things. She had lots of 'ideas' about what people with DS could and could not do. She had no idea from her dd's descriptions that Chrisitne was anything other then deaf. She went on to tell me that had totally changed her mind about people with DS and what they CAN do given the chance and some kid friendly pushing in the right direction. So I was happy I hadn't made a big deal of the DS and just let everyone kind of find their way. was present at all the concerts, so anyone who came ,knew! I DID print and give them lots of things from these two sites as the need arose - http://disabilityisnatural.com/ http://www.normemma.com/index.htm I was very blessed with the teacher who is my idea of a REAL teacher. She just loves teaching and kids in general. Has a real heart for people and just accepted was a kid like the rest and since she had never been around a person with DS, she really had no idea what to expect and I kinda just let make her own impression on everyone. This is really one of my very favorite articles and one that I made sure everyone dealing with had read http://www.normemma.com/arhellbe.htm I think it really sets the 'tone' I like to use regarding her DS. Carol in IL Talk is cheap. Use Messenger to make PC-to-Phone calls. Great rates starting at 1¢/min.

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Hi,

I also attended one of her workshops recently & was also very disappointed she

advocated

for parents to fight for time for their children in the special ed class rooms.

I strongly

support inclusion, so I was devastated that that is still being advocated from

within our

community so generalized to all children w/DS.

The Down Syndrome Educational Trust, located in the UK (downsed.org), is a great

resource for info on DS. They publish Down Syndrome Research & Practice, which

is a

" multidisciplinary peer-reviewed journal that publishes original research

papers, review

articles, abstracts and news to assist the international scientific research

community and

to inform professionals and parents involved in the care of individuals with

Down

syndrome of the latest scientific knowledge and its implications for good

practice. " That

being said, it is reliable information.

They have been doing research & have found that inclusive education benefits

children w/

DS, You can find a summary of the research here:

http://www.downsed.org/research/

projects/reports/2000/education/

I hope that helps!

>

> I believe this is the link to the study...I just did some searching and found

two " quotes "

from this " study " (and yes it is considered a study, altho I don't agree) in my

handout from

the presentation, so I think it is it. I didn't save it when I searched it out

last time.

>

> http://www.altonweb.com/cs/downsyndrome/index.htm?page=wolpert.html

>

> Below are the remarks that Peoples shared during her workshop. Again, I

wouldn't have a problem with this being reported if she would have given more

background information, such as this was a study done via a questionnaire of a

small

number of parents and teachers (who returned their questionnaire) and their

thoughts

about inclusion.

>

> Large groups and the whole class were reported not effective at all for

students with

Down syndrome.

>

> individualized instruction and small groups being the most effective.

>

>

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Thanks -- I will have to print this out read it.

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

From: Jill <thrill@...>

Date: Wed Jul 12 08:59:56 CDT 2006

Down Syndrome Treatment

Subject: Re: Re: Dual diagnosis school speech

I believe this is the link to the study...I just did some searching and found

two " quotes " from this " study " (and yes it is considered a study, altho I don't

agree) in my handout from the presentation, so I think it is it.  I didn't save

it when I searched it out last time. 

 http://www.altonweb.com/cs/downsyndrome/index.htm?page=wolpert.html Below are

the remarks that Peoples shared during her workshop.  Again, I wouldn't

have a problem with this being reported if she would have given more background

information, such as this was a study done via a questionnaire of a small number

of parents and teachers (who returned their questionnaire) and their thoughts

about inclusion. Large groups and the whole class were reported not effective at

all for students with Down syndrome. individualized instruction and small groups

being the most effective.    Re:

Dual diagnosis school speech

I thought about all this last year when entered kdgr and I

decided to do 'nothing'. ;-) Well ,I did loan some of my books on DS to

the teacher when she did her unit on differences. Nothing earth

shattering, just the ABC book featuring kids with DS, Paint the Octupus

Red, and My Brother has DS.  She does the same unit each year that covers

everything- glasses, deafness, skin color, general disability etc, so my

books fit right in and they read them with out much reference to

other then the same kinds they made about the different color of people's

eyes.   I opted out of the speech and bringing a lot of attention to

. I wasn't really sure if it 'worked' or not, other then the fact

that  the school year went really well and no one seemed to think much

about her being there... as in- no one questioned her being there.  

Towards the end of the year on the way h ome from a field trip, one of the

other moms who spent a lot of time in the room told me at the beginning of

the year her dd came home talking about all the time. All this

mom knew was couldn't talk as well as the other kids, but it was

'no big deal' to her dd.  uses sign language' which kids seem to

find fun and enjoy picking it up. The mom said her dd  had no idea about

DS, or what it meant, or even that there was such an animal. ;-)

Therefore, she treated the same as she would any other kid who

didn't talk so well, that really seemed to be the most interesting thing

about her with the other kids.   This mom was shocked ( her words ) when

she did come to the class room and found out toad had DS.  The reason she

was shocked??? Her cousin has DS and I guess he was quite the handfull and

not very capable of things. She had lots of 'ideas' about what people with

DS could and could not do. She had no idea from her dd's

descriptions that Chrisitne was anything other then deaf. She went on to

tell me that had totally changed her mind about people with DS

and what they CAN do given the chance and some  kid friendly pushing in

the right direction. So I was happy I hadn't made a big deal of the DS and

just let everyone kind of find their way. was present at all the

concerts, so anyone who came ,knew!   I DID print and give them lots of

things from these two sites as the need arose -

http://disabilityisnatural.com/ http://www.normemma.com/index.htm   I

was very blessed with the teacher who is my idea of a REAL teacher. She

just loves teaching and kids in general. Has a real heart for people and

just accepted was a kid like the rest and since she had never

been around a person with DS, she really had no idea what to expect and I

kinda just let make her own impression on everyone.   This is

really one of my very favorite articles and one that I made sure everyone

dealing with had read http://www.normemma.com/arhellbe.htm   I

think it really sets the 'tone' I like to use regarding her DS.   Carol in

IL

Talk is cheap. Use Messenger to make PC-to-Phone calls. Great rates

starting at 1¢/min.

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no the bag gets passed on to the gen ed teacher for the next year -- my TOR

(special needs teacher) helps make sure this happens at the end of the school

year -- we find out on the last day what the classroom assignments are for the

next year.

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

From: pbeurrier@...

Date: Wed Jul 12 07:59:46 CDT 2006

Down Syndrome Treatment

Subject: Re: Re: Dual diagnosis school speech

Do you get the books back each year? I've given the books to teachers but rarely

gotten anything back unless I went and got it! I don't really mind because the

information gets out more, but it does get expensive!

ette

---------

Re: [DownSyndromeInfoEx<WBR>change] Dual diagnosis school speech <BR><BR>I

thought about all this last year when entered kdgr and I decided to do

'nothing'. ;-) Well ,I did loan some of my books on DS to the teacher when she

did her unit on differences. Nothing earth shattering, just the ABC book

featuring kids with DS, Paint the Octupus Red, and My Brother has DS. She does

the same unit each year that covers everything- glasses, deafness, skin color,

general disability etc, so my books fit right in and they read them with out

much reference to other then the same kinds they made about the

different color of people's eyes. I opted out of the speech and bringing a lot

of attention to . I wasn't really sure if it 'worked' or not, other

then the fact that the school year went really well and no one seemed to think

much about her being there... as in- no one questioned her being there. Towards

the end of the year on the way h ome from a field trip, one of the other moms

who spent a lot of time in the room told me at the beginning of the year her dd

came home talking about all the time. All this mom knew was

couldn't talk as well as the other kids, but it was 'no big deal' to her dd.

uses sign language' which kids seem to find fun and enjoy picking it

up. The mom said her dd had no idea about DS, or what it meant, or even that

there was such an animal. ;-) Therefore, she treated the same as she

would any other kid who didn't talk so well, that really seemed to be the most

interesting thing about her with the other kids. This mom was shocked ( her

words ) when she did come to the class room and found out toad had DS. The

reason she was shocked??? Her cousin has DS and I guess he was quite the

handfull and not very capable of things. She had lots of 'ideas' about what

people with DS could and could not do. She had no idea from her dd's

descriptions that Chrisitne was anything other then deaf. She went on to tell me

that had totally changed her mind about people with DS and what they

CAN do given the chance and some kid friendly pushing in the right direction. So

I was happy I hadn't made a big deal of the DS and just let everyone kind of

find their way. was present at all the concerts, so anyone who came

,knew! I DID print and give them lots of things from these two sites as the need

arose - http://disabilityisnatural.com/ http://www.normemma.com/index.htm I was

very blessed with the teacher who is my idea of a REAL teacher. She just loves

teaching and kids in general. Has a real heart for people and just accepted

was a kid like the rest and since she had never been around a person

with DS, she really had no idea what to expect and I kinda just let

make her own impression on everyone. This is really one of my very favorite

articles and one that I made sure everyone dealing with had read

http://www.normemma.com/arhellbe.htm I think it really sets the 'tone' I like to

use regarding her DS. Carol in IL

Talk is cheap. Use Messenger to make PC-to-Phone calls. Great rates

starting at 1¢/min.

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