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My husband had a very pronounced Lewy Lean at times -

he leaned to the left on chairs, and if I wasn't

looking, he sometimes leaned so far he fell off. It

sometimes was quite a job to get him back up. He also

did this when walking, especially if it was very far.

One time when we were shopping, he was leaning so far

to the left, I thought he was going to fall over, and

I had to virtually hold him up until we got him to a

seat. I didn't know then what it was, but found that

out on the site later. Wished I would have known

before.

He also was very cold at home this past winter. Wore

a t-shirt, long-sleeved shirt, sat with a blanket

around his shoulders and sometimes whole body, by an

electric heater and still complained about being cold.

He is the NH now, and today it was 94 here. When I

got there late p.m. to be with him during dinner, he

had a coat on and said he was cold. AC was not that

cold either. So, both are obviously LBD symptoms.

Also runny nose for him. I have been reading today

that Aricept might be the cause of it and may ask them

to discontinue it to see if that might be the cause.

--- sissyp1102 wrote:

> i have noticed that my husband (diagonised with

> parkinsons and LBD)

> skin is always cool to the touch i ask him if he is

> cold sometimes he

> says yes sometimes he says no, also he is leaning to

> the right side i

> have tried to get him to set up straight but he says

> he cant, has

> anyone else come across this problem. thanks for

> your help, sissy

> lewis

>

>

>

>

>

>

>

>

__________________________________________________

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  • 1 year later...

Honestly....I don't think the doctor had ANY right to tell you who you

should tell, or not tell..........that's none of his/her business, and very OLD

SCHOOL thinking if you ask me!! I think I'd be irate. Maybe I am now..ahaha!

It's your decision as parents to tell who you want to tell..... rent a blimp

and have it streaming across the skies if you want to! I personally am for

telling............ first and foremost, it EDUCATES others. Also, you never

know how your daughter will do in the future...she may need say, speech

therapy, and if you've kept her diagnosis a secret from the schools,

etc............how will she get those services??

my 2 cents...

~~Angel~~

Mom to 14 mosaic Down syndrome/Hirschsprung's Disease

Lance 19, Tyler 15, 12

Jaeda 11 & Shayne 5

************************************** See what's new at http://www.aol.com

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Hi Sue

You are not alone in this! This seems to be the main question that comes up at

IMDSA! The doctor probably didn't mean " behaviors " as in " she is going to act

bad " . More than likely the doctor meant that if she acted " differently " or had

trouble with certain things, then you would have to explain the problem to

people (mainly teachers)

When Tim was younger, I did not tell anyone about his MDS. I wanted them to

know him for who he was, not what he had. I wanted them to not limit him because

I had seen times where people who knew about his dx automatically expected less

from him. When I did tell people, I first waited several weeks for them to get

to know him. That way, they expected him to act like everyone else and learn

like everyone else. Then, I would tell them about his MDS (especially teachers)

and I would tell them what I expected from him and what I expected from the

teachers. There were times that I did not tell the teachers at all. These times,

I can see where it was beneficial in one way (they expected the same from him as

they did everyone else) and hurtful in other ways (if he acted differently or

had trouble with his work they treated him too harshly for something he was

completely incapable of helping)

So, It is a preference for each family to decide and no solution is the

" wrong " solution! You do what is best for you and your family!

Tim and I talked about this situation (about not telling) with one of our

members, Sosnoski on National Public Radio's This American Life. If you

are interested in hearing our story, you can go to

http://www.thislife.org/Radio_Episode.aspx?sched=1128

and click the orange speaker button. (our story is right after the

introduction on " mouse traps " .

I hope it helps.

Kristy

Sue wrote:

Hi Everyone,

I have a bit of a dilemma. We were at the doctors last week.. We went to a

genetic specialist and to the ds clinic. On doctor suggested we do not tell

anyone that Isabella has mds and xxx, so it would not label her. The other

doctor said we would always have to be explaining her behavior. Isabella does

not have the physical characteristics of ds so I guess the one doctor figured

nobody would know. I am not ashamed she has mds or xxx, this was out of our

control and we love her just the same, maybe more if that is possible. I am

still trying to figure out what the other doctor meant by explaining her

behavior when she get older. Just what does she think she will act like or do? I

have told my family and close friends its not some dirty little secret, yet now

I am afraid it will label her. Any suggestions on what all of you have done in

this situation.

Sue

__________________________________________________

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  • 3 weeks later...

Here is a link to www.snopes.com regarding a similar story floating

around about the re-use of plastic water bottles. Apparently, it's just

another one of those urban legends.

http://www.snopes.com/medical/toxins/petbottles.asp

A.

Special Educator

Simon Kenton High School

(859)960-0348

cynthia.jones@...

" Deaf People Can Do Anything Except Hear! " (I. King Jordan)

Confidentiality Notice - This email is intended only for the person to

whom it is addressed and may contain confidential information. Any

unauthorized review is prohibited. If you are not the intended

recipient, kindly contact the sender by reply email and destroy all

copies of the original message. If you are the intended recipient, but

do not wish to receive communication through this medium, please advise

the sender immediately.

(unknown)

I know everyday they are recalling different things. This is not a

recall but is scared me enough to change to glass bottles. I just

wanted to pass this along to those of you that have babies.

Products marketed for infants and children are not always completely

safe for their use. Many contain toxic chemicals that may have

detrimental health impacts for children exposed during critical stages

of development. In this report, we analyze the extent to which five

popular brands of baby bottles leach bisphenol A, a developmental,

neural, and reproductive toxicant, into liquids coming into contact with

them. We found that all five brands leach bisphenol A at dangerous

levels found to cause harm in numerous laboratory animal studies.

California and the U.S. should reform chemical policy to ensure that all

products on the market are safe for children.

Bisphenol A is a Developmental, Neural, and Reproductive Toxicant

Scientists have linked very low doses of bisphenol A exposure to

cancers, impaired immune function, early onset of puberty, obesity,

diabetes, and hyperactivity, among other problems.

For example, in one recent study, a single, low dose of bisphenol A

administered to a newborn rat resulted in hyperactive behavior.

Exposure to Bisphenol A is Widespread

Bisphenol A is most commonly used to make clear polycarbonate plastic

for consumer products, such as baby bottles. Through use, this plastic

breaks down and leaches bisphenol A into liquids and food to which it

comes into contact.

The U.S. Centers for Disease Control and Prevention found bisphenol A in

the urine of over 95% of people they tested.

Alarmingly, the median level of bisphenol A in humans is higher than the

level that causes adverse effects in animal studies.

Popular Baby Bottles Sold in California Leach Bisphenol A at Harmful

Levels

Based on a consumer survey of the most popular baby bottle brands on the

market, we selected five bottle types to determine the amount of

leaching from each bottle. We found that the bottles tested from all

five brands leached bisphenol A at levels found to cause harm in

numerous laboratory studies, including:

* Avent

* Dr. Brown's

* Evenflo

* Gerber

* Playtex

Recommendations for Parents

Parents have the right to know about chemicals in the products they

purchase for their children. In the absence of good government

regulations, but armed with the knowledge that some chemicals are a

cause for concern, parents can take a few simple actions to limit their

child's exposure to these and other toxic chemicals.

At the store, parents should select baby bottles that are made from

glass or a safer non-polycarbonate plastic. At home, parents should

avoid washing plastic dishware with harsh dishwashing soap and hot

water, which may allow chemicals to leach out of the plastic. For a

useful tip sheet, parents should visit our toy safety page.

Recommendations for Policymakers

Parents cannot deal with these issues alone. The government must ensure

the safety of all products on the market for children. California and

the U.S. should:

Phase Out Hazardous Chemicals

Based on the weight of the scientific evidence showing the harm caused

by exposure to bisphenol A, the government should act now. Given that

data from the U.S. Centers for Disease Control and Prevention show that

bisphenol A is present in humans at levels found to be harmful in

laboratory studies, California and the U.S. should phase out the use of

bisphenol A, especially in products used by children.

Inform Consumers about the Presence of Dangerous Chemicals

Parents currently have little information to inform their decisions when

purchasing products for their family. Manufacturers should be required

to label children's products with the name of any potentially dangerous

chemical and the specific health risks associated with the chemical.

Reform Chemicals Policy

Currently, manufacturers can put chemicals on the market without proving

they are safe. Chemical manufacturers should be required to provide all

hazard and health-effects information to the government so agencies can

begin to assess the thousands of chemicals currently on the market for

which little or inadequate data are available. Next, pre-market hazard

and health-effects testing should be required for all new chemicals

before they are introduced into commerce. Finally, the California

Environmental Protection Agency must have the authority to protect

public health by banning or restricting the use of a chemical if

evidence shows that it can harm human health.

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Sue

I totally agree with you. The misuse of this word is heartbreaking. IMDSA

focused on the misuse of the word retarded in our latest issue of MOSAIC WORLD.

Were you able to read that along with the Parent's Perspective that did?

(I can't remember if you receive our newsletter or not) If you did read it, what

did you think about the article?

Kristy

dewardjohnson@... wrote:

Just yesterday I posted a note about the word " retard " being used.

Don't you know that today I found it being used in a very derogatory way in the

" heading " of a posting in a group in CafeMom. Needless to say I blasted the

person for using this terminology and posted a note in my other DS groups. I

also sent a note to the group leader where this word was posted. They block or

lock any other terminology that would be offensive to any other group, but not

this? Why do we just stand by and let this phrase be used without causing a

stir. I have never liked that word. I watched my best friend have to defend her

brother (brain damaged) her whole life and what a struggle it was for her and

her brother. She is now 41 and her childhood and that word still haunts her! I

for one do not want my daughter growing up in a society that feels this word is

okay to use.

I am sorry for ranting again, it is just that my blood is boiling.

Sue

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No unfortunately I have not been able to join the IMDSA group yet. Hopefully

after Christmas I will.

I am so glad you agree with me though.

Sue

-------------- Original message --------------

Sue

I totally agree with you. The misuse of this word is heartbreaking. IMDSA

focused on the misuse of the word retarded in our latest issue of MOSAIC WORLD.

Were you able to read that along with the Parent's Perspective that did?

(I can't remember if you receive our newsletter or not) If you did read it, what

did you think about the article?

Kristy

dewardjohnson@... wrote:

Just yesterday I posted a note about the word " retard " being used. Don't you

know that today I found it being used in a very derogatory way in the

" heading " of a posting in a group in CafeMom. Needless to say I blasted the

person for using this terminology and posted a note in my other DS groups. I

also sent a note to the group leader where this word was posted. They block or

lock any other terminology that would be offensive to any other group, but not

this? Why do we just stand by and let this phrase be used without causing a

stir. I have never liked that word. I watched my best friend have to defend her

brother (brain damaged) her whole life and what a struggle it was for her and

her brother. She is now 41 and her childhood and that word still haunts her! I

for one do not want my daughter growing up in a society that feels this word is

okay to use.

I am sorry for ranting again, it is just that my blood is boiling.

Sue

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You are so right!

From: MosaicDS [mailto:MosaicDS ] On Behalf

Of dewardjohnson@...

Sent: Saturday, November 17, 2007 9:50 AM

To: Mosaic DS Group

Subject: (unknown)

Just yesterday I posted a note about the word " retard " being used. Don't you

know that today I found it being used in a very derogatory way in the

" heading " of a posting in a group in CafeMom. Needless to say I blasted the

person for using this terminology and posted a note in my other DS groups. I

also sent a note to the group leader where this word was posted. They block

or lock any other terminology that would be offensive to any other group,

but not this? Why do we just stand by and let this phrase be used without

causing a stir. I have never liked that word. I watched my best friend have

to defend her brother (brain damaged) her whole life and what a struggle it

was for her and her brother. She is now 41 and her childhood and that word

still haunts her! I for one do not want my daughter growing up in a society

that feels this word is okay to use.

I am sorry for ranting again, it is just that my blood is boiling.

Sue

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  • 2 weeks later...

Bet they wouldn't be throwing the " N " word around like that now would they??

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

Be a better sports nut! Let your teams follow you with Yahoo Mobile. Try it now.

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Yea for Isabella! You may never see any delays! Remember, there are many people

out there who have MDS and don't even know it!

Kristy

dewardjohnson@... wrote:

Hi all just got back from a well visit with Isabella pediatrician.

They were so pleased at her progress but also dumbfounded. The doctor said that

she has been in touch with the DS clinic and the genetic doctor and they are all

scratching their heads. All of the reports they get on her shows she has mds and

xxx yet they have found no delays so far. I am taking that for all it is worth

and I am very happy with the news. I know that we do not know what the future

hold but she seems to be off to such a great start.

Sue

Isabella 11 months

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My daughter just got done with her PT. Her therapist brought up the MDS again

because of what all she is doing. I got a laugh when the therapist said in

January we would be working on getting her to climb stairs. I started laughing

and told her that she taught herself during the past month. So now we have to

find something else to challenge her to do. Maybe one day I can get her retested

for MDS.

Re: (unknown)

Yea for Isabella! You may never see any delays! Remember, there are many

people out there who have MDS and don't even know it!

Kristy

dewardjohnson@... wrote:

Hi all just got back from a well visit with Isabella pediatrician. They were

so pleased at her progress but also dumbfounded. The doctor said that she has

been in touch with the DS clinic and the genetic doctor and they are all

scratching their heads. All of the reports they get on her shows she has mds and

xxx yet they have found no delays so far. I am taking that for all it is worth

and I am very happy with the news. I know that we do not know what the future

hold but she seems to be off to such a great start.

Sue

Isabella 11 months

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I actually belong to the DS group this woman belongs to and it's legit.

God Bless,

Rowe

www.myspace.com/beckyrowe5150

(unknown)

I just read this in cafemom and found it interesting. I thought maybe Kristy or

someone with a lot of knowledge about MDS would be interested in contacting this

show, to educate people on mds. I have copyed the letter from cafemom below

Sue (Isabella 11 months)

HYH Radio is an inspiration and information online talk show that is due to

launch January 6, 2008 and will air every Sunday. A 30-Minute show dedicated to

empowering women and discussing informative and inspirational topics for parents

of Special Needs Children.

If you would like to be a guest on the show, please visit www.hyhradio. com for

more information and click on the " Suggest a Guest " button. You can Also contact

Ms. Teri Kendle " Broadcast Assistant " directly at Imani4290yahoo (DOT) com.

Please Add: HYH Radio to your Myspace Page : www.myspace. com/hyhradio and

www.myspace. com/imaniinsac

Thank You

Ms. Teri Kendle

Broadcast Assistant

Pierre

Host/ Executive Director/ Producer

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and I are friends and I will speak with her concerning doing a radio

program. I am just too busy right now to even try to schedule anything.

Kristy

Becky Rowe wrote:

I actually belong to the DS group this woman belongs to and it's

legit.

God Bless,

Rowe

www.myspace.com/beckyrowe5150

(unknown)

I just read this in cafemom and found it interesting. I thought maybe Kristy or

someone with a lot of knowledge about MDS would be interested in contacting this

show, to educate people on mds. I have copyed the letter from cafemom below

Sue (Isabella 11 months)

HYH Radio is an inspiration and information online talk show that is due to

launch January 6, 2008 and will air every Sunday. A 30-Minute show dedicated to

empowering women and discussing informative and inspirational topics for parents

of Special Needs Children.

If you would like to be a guest on the show, please visit www.hyhradio. com for

more information and click on the " Suggest a Guest " button. You can Also contact

Ms. Teri Kendle " Broadcast Assistant " directly at Imani4290yahoo (DOT) com.

Please Add: HYH Radio to your Myspace Page : www.myspace. com/hyhradio and

www.myspace. com/imaniinsac

Thank You

Ms. Teri Kendle

Broadcast Assistant

Pierre

Host/ Executive Director/ Producer

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Hi ,

I am probably not the best to answer that question because I only found out

recently also about my daughter. I can tell you what testing they have done so

far. The first place we were sent after the geneticist was the Down Syndrome

Clinic. We were then sent to the cardiologist go make sure Isabella heart was

okay and it was fine. There was an eye problem but that is how we found out

about mds in the first place. My daughter is farsighted. We had to go for

routine blood work which included a check on her thyroid. This week we were

scheduled for hearing test. Although with her not feeling well I think I will

put that off until January. Isabella tested fine in every area except for one

eye. I like you was asking what more can I do. The answer I got from everyone

was just love you child the same. I don't love her the same anymore, I Love her

MORE!

Merry Christmas

Sue (Isabella almost 1)

-------------- Original message --------------

Howdy all. I've been following along with some of the discussion although I

haven't participated much. I just wanted to ask all of you that have been

dealing with this longer than we have. What more should we be doing?

is 5 1/2 and was diagnosed just before Thanksgiving. He is currently in

speach therapy and in the special needs program in his kindergarten. We have an

appointment with a genetecist in January. What else should we be doing for him?

Thanks for all your help!

(5-mds) Nick and Sam (3)

__________________________________________________________

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The testing sounds about right -- x-rays, blood tests,

eyes.... Olivia is 9 (she needs to go in for more

testing recommmended by her pediatrician, as the dr

thinks she may be going through puberty SUPER ealry --

which, from what I've been told isn't unusual. Then

there's the trips to the dentist -- the bottom teeth

don't line up with the top teeth ... I'm still

researching why this happened, but I know people can

have bad teeth.... braces are going to be

interesting....

but yes,

the love part definitely goes without saying.

The academics part though is tough. Finding the

" right " place is truly challenging. She's smart

enough to be educated in a " typical " classroom. Even

though all kinds of educated specialists can be found

at a " special classrom " the facility itself is, well,

not exactly what I want for my kid.

Public schools are too overcrowded & poorly equiped to

" deal with " children with special needs -- or so I

have been told by " people " in the administration.

Yes, it's a violation of my child's rights to even be

told that, but it seems the more you fight for your

kid and even though you " get " what you fight for,

following through is even tougher -- working with

people who aren't properly educated/trained, or who

are way too overwhelmed trying to accomodate everyone

.... well, yeah, it is incredibly frustrating.

Being a single mom, I'm lucky that I have great

employers who are " cool " with me taking time off to

investigate schools, having IEPS (loved that Dr. Seuss

poem that was circulated not too long ago), going to

speech sessions, etc.

You have to do it. The road doesn't seem to get

easier. I don't know if it's supposed to. I figure

the ultimate goal is to have Olivia be

self-sufficient, confident, secure, and willing to be

part of society. She takes dance, swimming,

singing.... constantly keeping her busy, involved &

active.... there will always be a lot to do, a lot to

look forward to...

having a lot of patience & a lot of love

helps a lot

too

and of course all those wonderful hugs & kisses that

make everything seem a-ok.

- Sophia

--- dewardjohnson@... wrote:

> Hi ,

> I am probably not the best to answer that question

> because I only found out recently also about my

> daughter. I can tell you what testing they have

> done so far. The first place we were sent after the

> geneticist was the Down Syndrome Clinic. We were

> then sent to the cardiologist go make sure Isabella

> heart was okay and it was fine. There was an eye

> problem but that is how we found out about mds in

> the first place. My daughter is farsighted. We had

> to go for routine blood work which included a check

> on her thyroid. This week we were scheduled for

> hearing test. Although with her not feeling well I

> think I will put that off until January. Isabella

> tested fine in every area except for one eye. I

> like you was asking what more can I do. The answer

> I got from everyone was just love you child the

> same. I don't love her the same anymore, I Love her

> MORE!

> Merry Christmas

> Sue (Isabella almost 1)

>

> -------------- Original message --------------

>

> Howdy all. I've been following along with some of

> the discussion although I haven't participated much.

> I just wanted to ask all of you that have been

> dealing with this longer than we have. What more

> should we be doing?

>

> is 5 1/2 and was diagnosed just before

> Thanksgiving. He is currently in speach therapy and

> in the special needs program in his kindergarten. We

> have an appointment with a genetecist in January.

> What else should we be doing for him?

>

> Thanks for all your help!

>

>

>

> (5-mds) Nick and Sam (3)

>

>

__________________________________________________________

> Be a better friend, newshound, and

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

>

http://mobile.yahoo.com/;_ylt=Ahu06i62sR8HDtDypao8Wcj9tAcJ

>

>

> [Non-text portions of this message have been

> removed]

>

>

>

>

> [Non-text portions of this message have been

> removed]

>

>

>

> Become a member of IMDSA today at

> http://www.imdsa.com

>

*******************************************************

> Purchase your MDS awareness bracelet today!

> http://www.imdsa.com/bracelets

>

**************************************************************************

> Contact IMDSA Today at:

> IMDSA~PO Box

>

1052~lin,TX~77856~USA~1-~1-888-MDS-LINK

>

*********************************************************************

> Share your story today!

> http://www.mosaicdownsyndrome.com

>

*********************************************************

>

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I just noticed that we have several 5 year old boys who's names start with " A " .

Our Adam is also 5 1/2 and in kindergarten. Sounds like you are doing fine. My

advice to you is to stay on top of his school program. I know we have to push

for Adam because he has a big speech delay, so teachers tend to act like he

doesn't know anything. Since I work in an elementary school, I was able to get

my hands on the kindergarten materials and we do some of this with him at home.

He is able to read some words and is very good with letters and numbers, but

when he can't tell the teacher, they just put it on the back burner. Just don't

expect them to teach him everything he needs to know.

Donna - gram to Adam 5 mds, Skylar 5 and Mia 1

Membership Chairperson

Hailey wrote:

Howdy all. I've been following along with some of the discussion

although I haven't participated much. I just wanted to ask all of you that have

been dealing with this longer than we have. What more should we be doing?

is 5 1/2 and was diagnosed just before Thanksgiving. He is currently in

speach therapy and in the special needs program in his kindergarten. We have an

appointment with a genetecist in January. What else should we be doing for him?

Thanks for all your help!

(5-mds) Nick and Sam (3)

__________________________________________________________

Be a better friend, newshound, and

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

http://mobile.yahoo.com/;_ylt=Ahu06i62sR8HDtDypao8Wcj9tAcJ

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,

Mahrya is in 5th grade and is 11 years old. We made sure we did what the

therepists suggested, then we treated her just like any one of our other kids.

We always felt it was important to give her all the different kinds of

expiriences that we could, which wasn't hard with her being the youngest of 6.

She went to basketball games, the beach, amusement parks, the zoo ect.. All

these different things have " learning moments " that don't seem like learning.

She is now a very outgoing girl, who has a wonderful snese of adventure. She

does not see herself as different from other children at all. I don't think she

realizes that she has real academic delays, she is just one of the kids.

Luanne mom to Mahrya 11 mds, Ben 12, Alan 19, Sandy 21, Steve 23, Dan 24 and

grandma to 3, 11 mo, and Elaina Rose born just yesterday!!

Hailey wrote:

Howdy all. I've been following along with some of the discussion

although I haven't participated much. I just wanted to ask all of you that have

been dealing with this longer than we have. What more should we be doing?

is 5 1/2 and was diagnosed just before Thanksgiving. He is currently in

speach therapy and in the special needs program in his kindergarten. We have an

appointment with a genetecist in January. What else should we be doing for him?

Thanks for all your help!

(5-mds) Nick and Sam (3)

__________________________________________________________

Be a better friend, newshound, and

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

http://mobile.yahoo.com/;_ylt=Ahu06i62sR8HDtDypao8Wcj9tAcJ

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Happy Birthday Isabella! mom to Adde

dewardjohnson@... wrote: Well today is the big day. It is

Isabella 1st birthday. I can not believe a whole year has gone by. I look back

at videos from last year and oh my how she has grown. She is becoming so

independent and wanting to explore so much on her own. Last night she refused to

eat unless she could feed herself with a spoon. She actually did pretty well, of

course I had to change her clothes when she was done but most of it hit her

mouth. She no longer wants a bottle unless it is first thing in the morning. I

miss holding my baby and giving her the bottle but I guess it is her way of

saying she is becoming a big girl and I better get use to it. We have a very

special day planned. We are going to get her all dressed up and go see Santa and

have her picture taken. Not to sure how that will go because she has decided in

the last 2 weeks she does not like strangers to pick her up. Then tonight we are

going to have the party that was planned for last

week. Well I have to go for now, if

I do not have a chance before Christmas I just wanted to wish everyone a Merry

Christmas, Happy Holidays and Happy New Year. I hope all of your dreams come

true.

Sue

Isabella 1 year old

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Sue,

Just so you know, we expect to see pictures of " our " big girl with Santa later

LOL!

Merry Christmas and Happy New Year Everyone! I'm off to Austin's first school

Christmas Party.....Santa will be arriving sometime during the party! I will be

taking pictures (and I'll post them too!)

God Bless,

Rowe

www.myspace.com/beckyrowe5150

(unknown)

Well today is the big day. It is Isabella 1st birthday. I can not believe a

whole year has gone by. I look back at videos from last year and oh my how she

has grown. She is becoming so independent and wanting to explore so much on her

own. Last night she refused to eat unless she could feed herself with a spoon.

She actually did pretty well, of course I had to change her clothes when she was

done but most of it hit her mouth. She no longer wants a bottle unless it is

first thing in the morning. I miss holding my baby and giving her the bottle but

I guess it is her way of saying she is becoming a big girl and I better get use

to it. We have a very special day planned. We are going to get her all dressed

up and go see Santa and have her picture taken. Not to sure how that will go

because she has decided in the last 2 weeks she does not like strangers to pick

her up. Then tonight we are going to have the party that was planned for last

week. Well I have to

go for now, if

I do not have a chance before Christmas I just wanted to wish everyone a Merry

Christmas, Happy Holidays and Happy New Year. I hope all of your dreams come

true.

Sue

Isabella 1 year old

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Oh a Christmas party, how fun. I hope you and Autin have a wonderful day.

Sue

--------- (unknown)

Well today is the big day. It is Isabella 1st birthday. I can not believe a

whole year has gone by. I look back at videos from last year and oh my how she

has grown. She is becoming so independent and wanting to explore so much on her

own. Last night she refused to eat unless she could feed herself with a spoon.

She actually did pretty well, of course I had to change her clothes when she was

done but most of it hit her mouth. She no longer wants a bottle unless it is

first thing in the morning. I miss holding my baby and giving her the bottle but

I guess it is her way of saying she is becoming a big girl and I better get use

to it. We have a very special day planned. We are going to get her all dressed

up and go see Santa and have her picture taken. Not to sure how that will go

because she has decided in the last 2 weeks she does not like strangers to pick

her up. Then tonight we are going to have the party that was planned for last

week. Well I have to

go for now, if

I do not have a chance before Christmas I just wanted to wish everyone a Merry

Christmas, Happy Holidays and Happy New Year. I hope all of your dreams come

true.

Sue

Isabella 1 year old

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  • 3 years later...
Guest guest

I would send my child to spite them...

Carolyn

To: Texas-Autism-Advocacy Sent: Saturday, April 16, 2011 8:28 AMSubject: Re: (unknown)

I assume he would not be taking the TAKS?? Don't they have a gym or cafeteria where those who are not taking TAKS can be with some supervised activities? I don't see how they can deny him access?>> Whst would you all do if your child's teacher said he needs to stay home on taks day because he may be loud and a distraction for the nearby 5th grade class. Are they allowed to do this?> > Sent from my iPad>

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Guest guest

No he will not be taking the TAKS. They fear he will make noise from his classroom which is close to the 5th graders. Sent from my iPad

I assume he would not be taking the TAKS?? Don't they have a gym or cafeteria where those who are not taking TAKS can be with some supervised activities? I don't see how they can deny him access?

>

> Whst would you all do if your child's teacher said he needs to stay home on taks day because he may be loud and a distraction for the nearby 5th grade class. Are they allowed to do this?

>

> Sent from my iPad

>

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Guest guest

I was going to say the same thing did. I also think the child has a right to be at school, but I would also consider where they would be putting my child and with whom so that it was in my child's best interest to be there. I hate the idea of a desk in a busy office or a quiet room where they were not being monitored or engaged. My feeling is that it should be as regular a day at school as possible unless they have it in the IEP that the child stays at home on testing days-not likely! Telling you to keep your child home raises all of our eyebrows. I wonder what the district or the media would think of this policy. Smells bad.Fran

I would send my child to spite them...

Carolyn

To: Texas-Autism-Advocacy Sent: Saturday, April 16, 2011 8:28 AMSubject: Re: (unknown)

I assume he would not be taking the TAKS?? Don't they have a gym or cafeteria where those who are not taking TAKS can be with some supervised activities? I don't see how they can deny him access?>> Whst would you all do if your child's teacher said he needs to stay home on taks day because he may be loud and a distraction for the nearby 5th grade class. Are they allowed to do this?> > Sent from my iPad>

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  • 2 weeks later...
Guest guest

I agree I would talk to Noy. I doubt she aware this is going on.

 

 

My ASD son is in life skills (FAC) in Round Rock, and all the (often disruptive) kids in his class, including him, are all attending school as usual this week during TAKS testing. Is your son in general ed? At my son's school, the special ed kids who spend most of their time in general ed and/or resource still come to school on TAKS testing days - no one would ever dream of asking them to stay home. I think they end up spending the day 100% in resource rather than in the general ed classroom where the testing is going on (it is true that if there is a disruption in the classroom where testing is going on, TEA requires that a special form be filled out explaining why the testing environment was " contaminated " - those are their words - and the tests of the students in that classroom are, indeed, null and void). However, most (good) schools make accommodations for this possibility by assigning staff to be one-on-one with students who need that to either take the test or keep from disrupting others who are taking the test. For sure they don't ask that they stay home.

It sounds like your school doesn't have a very good plan for dealing with special ed students on TAKS testing days. I just wanted to let you know that not all RRISD schools are like that! I would definitely complain to the head of RRISD special ed ( Noy). I am nearly positive that they are not allowed to ask you to keep your son home.

-

> > > > >   > > > > > > which school district??????>

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Guest guest

I asked my son's FAC teacher today, and no RRISD teachers are allowed to ask

students to stay home on TAKS testing days. If they are thought to be

potentially disruptive, it is up to the teacher / school to make accommodations

for him on those days (e.g. assign a one-on-one aide and have him tested and/or

taught separately from the rest of the class that is testing).

-

>

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>

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> which school district??????

>

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