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First of all, I'd like to wish everyone a Happy New Year. I may be cheating in

my reply,

but it is easier for me to address multiple people in 1 posting, so I hope this

doesn't

offend anyone!

Congratulations EMILY on your new addition. I too, will be joining you very

soon in

becoming a mom of 3 (although I think you have your hands fuller than me with

young twins & a newborn!)

DANIELLE, my 10 year-old son used to have very significant issue with sensory

integration dysfunction, so muh so that he would either vomit at the sight of

things

that bothered him or turning blue & needing oxygen. You indicated that Coby has

always had small sensory issues that you didn't think were necessary to address.

The

issues of touching grass, sand, rice, etc. may be indicators of sensory

integration

dysfunction & should be addressed either by an OT or you can do some activities

with

Coby yourself to help him with this. There are other things that may indicate a

more

serious sensory problem such as inability to eat or touch certain textures of

food, not

liking to wear certain clothing fabrics or any clothes at all, not liking to be

hugged or

cuddled, not liking to get dirty, unable to adjust to hot or cold temperatures,

not

getting dizzy when most people would, & the list goes on... As much as any of

these

activitites may make him scream, repetition & time does break kids of sensory

disorders. If Coby has difficulty with any of the things I mentioned above, you

can do

some of the following activities with him: brushing his body with a soft bristle

brush

(like the ones they use in hospitals to scrub before entering the operating

room), lots

of spinning and swinging activities on the playground, encouraging him to walk

barefoot in sand and grass, playing with messy things such as finger painting,

shaving cream, play-doh, dirt, glue, etc., having him help you in cooking

activities in

which he has to touch messy or sticky ingredients such as peanut butter, melted

marshmallow (as in rice krispy treats), cookie dough, and playing with rice and

dry

beans. After years of therapy with my son, his sensory issues are minimal if

any now.

My son had years of OT to alleviate this problem among others. He has never had

an

issue with bathing that I can recall, but he still freaks out a little in the

shower when

the water is coming down over his head.

SONIA, you asked about your son reaching certain milestones, being a RSS child.

My

experience was that all gross motor milestones were pretty delayed. I am not

sure if

this is true for all RSS babies, but when my son was a baby, his head appeared

much

bigger than the rest of his body. This made it hard for him to be able to sit

up &

support the weight of his head until he " grew into it " . He also had weak muscle

tone.

He had & still has dimples in his shoulder blades. I am not sure if this has to

do with

muscle tone, strength, etc. but I think it also may have been a factor in upper

body

strength. I like to equate my son's milestones not with his age, but with his

size. He

sat up, rolled over, walked, etc. when he was the height/weight of typical

children

that reach those milestones. For example, he was 28 months when he walked, and

at

that age he was the size of a typical 9-12 month old (the age when most kids

walk).

Try not to get too stressed about any developmental delays may encounter.

If

you are doing therapy with him, you are doing all you can & he will eventually

catch

up to his peers.

MARY, I loved your post about being a parent to a RSS child. What a great

outlook &

sense of humor you have!

I am not sure who originally addressed the nighttime bed wetting. Fortunately I

didn't

encounter this problem with either of my children, although (RSS) potty-

trained a bit later than the norm. However, I just thought I'd share that I was

at the

park last week with a friend of mine & she has an 8 year-old & a six-year-old

boy

who both still wear pull-ups at night. Her oldest son, who is 9, doesn't have

this

problem. Her children are normal & I consider her to be a super mom! Just goes

to

show you that there are lots of other parents out there dealing with the same

issue,

RSS or not. Maybe this isn't just a RSS thing????

Last, but not least, JODIE, my son has ADHD & has taken medication for this off

& on

since he was 7-years-old. This is hard to diagnose in a young child & usually

becomes more of an issue when a child is in grade school. Most of the

medications

used to treat ADHD are stimulants (controlled substances), although there is one

that

has been on the market for about a year or so that is not a stimulant

(Strattera). You

can probably find a website somewhere using a search engine that has a parent

questionnaire you can fill out to see if your child is likely to have ADHD, but

even is

you think he does, the chances of getting him on medication at such a young age

would be slim.

I apologize again for my long post, but I hope my replies were helpful...

Kim (mom to , 10, RSS, , 3, and baby-to-be in February)

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Kim. your theory on the dimples in the shoulders is interesting. I remeber when

Immi was a baby and the docs were looking for a diagnosis (actually they had a

good idea that she was RSS right from the start but didn't feel that I should be

let in on this secret until she was officially diadnosed by a geneticist at

Great Ormand Street....we couldn't get an appointment til she was 9

months......but hey...I'm only her mother!!)Anyway...the docs were very

interested in the dimples in her shoulders but never offered any info into why

they might be there!

I also agree with you about the milestones.....they just have to wait until they

are big and strong enough thats all. Imogen is very small so she didn't walk til

she was 3....when she was 3 she was the size of a 12-15 month old....the average

age for 'normal' kids to walk.

The only sensory problem Imogen has is a dislike of loud noise(fireworks,cinema

ads,groups of children shouting excitedly) we have to brief her thoroughly

before we go anywhere 'loud' or she freaks. Is this just an Immism??

Happy New Year

Eileen

Kacey171 capuano_k@...> wrote:

First of all, I'd like to wish everyone a Happy New Year. I may be cheating in

my reply,

but it is easier for me to address multiple people in 1 posting, so I hope this

doesn't

offend anyone!

Congratulations EMILY on your new addition. I too, will be joining you very

soon in

becoming a mom of 3 (although I think you have your hands fuller than me with

young twins & a newborn!)

DANIELLE, my 10 year-old son used to have very significant issue with sensory

integration dysfunction, so muh so that he would either vomit at the sight of

things

that bothered him or turning blue & needing oxygen. You indicated that Coby has

always had small sensory issues that you didn't think were necessary to address.

The

issues of touching grass, sand, rice, etc. may be indicators of sensory

integration

dysfunction & should be addressed either by an OT or you can do some activities

with

Coby yourself to help him with this. There are other things that may indicate a

more

serious sensory problem such as inability to eat or touch certain textures of

food, not

liking to wear certain clothing fabrics or any clothes at all, not liking to be

hugged or

cuddled, not liking to get dirty, unable to adjust to hot or cold temperatures,

not

getting dizzy when most people would, & the list goes on... As much as any of

these

activitites may make him scream, repetition & time does break kids of sensory

disorders. If Coby has difficulty with any of the things I mentioned above, you

can do

some of the following activities with him: brushing his body with a soft bristle

brush

(like the ones they use in hospitals to scrub before entering the operating

room), lots

of spinning and swinging activities on the playground, encouraging him to walk

barefoot in sand and grass, playing with messy things such as finger painting,

shaving cream, play-doh, dirt, glue, etc., having him help you in cooking

activities in

which he has to touch messy or sticky ingredients such as peanut butter, melted

marshmallow (as in rice krispy treats), cookie dough, and playing with rice and

dry

beans. After years of therapy with my son, his sensory issues are minimal if

any now.

My son had years of OT to alleviate this problem among others. He has never had

an

issue with bathing that I can recall, but he still freaks out a little in the

shower when

the water is coming down over his head.

SONIA, you asked about your son reaching certain milestones, being a RSS child.

My

experience was that all gross motor milestones were pretty delayed. I am not

sure if

this is true for all RSS babies, but when my son was a baby, his head appeared

much

bigger than the rest of his body. This made it hard for him to be able to sit

up &

support the weight of his head until he " grew into it " . He also had weak muscle

tone.

He had & still has dimples in his shoulder blades. I am not sure if this has to

do with

muscle tone, strength, etc. but I think it also may have been a factor in upper

body

strength. I like to equate my son's milestones not with his age, but with his

size. He

sat up, rolled over, walked, etc. when he was the height/weight of typical

children

that reach those milestones. For example, he was 28 months when he walked, and

at

that age he was the size of a typical 9-12 month old (the age when most kids

walk).

Try not to get too stressed about any developmental delays may encounter.

If

you are doing therapy with him, you are doing all you can & he will eventually

catch

up to his peers.

MARY, I loved your post about being a parent to a RSS child. What a great

outlook &

sense of humor you have!

I am not sure who originally addressed the nighttime bed wetting. Fortunately I

didn't

encounter this problem with either of my children, although (RSS) potty-

trained a bit later than the norm. However, I just thought I'd share that I was

at the

park last week with a friend of mine & she has an 8 year-old & a six-year-old

boy

who both still wear pull-ups at night. Her oldest son, who is 9, doesn't have

this

problem. Her children are normal & I consider her to be a super mom! Just goes

to

show you that there are lots of other parents out there dealing with the same

issue,

RSS or not. Maybe this isn't just a RSS thing????

Last, but not least, JODIE, my son has ADHD & has taken medication for this off

& on

since he was 7-years-old. This is hard to diagnose in a young child & usually

becomes more of an issue when a child is in grade school. Most of the

medications

used to treat ADHD are stimulants (controlled substances), although there is one

that

has been on the market for about a year or so that is not a stimulant

(Strattera). You

can probably find a website somewhere using a search engine that has a parent

questionnaire you can fill out to see if your child is likely to have ADHD, but

even is

you think he does, the chances of getting him on medication at such a young age

would be slim.

I apologize again for my long post, but I hope my replies were helpful...

Kim (mom to , 10, RSS, , 3, and baby-to-be in February)

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

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hi kim!

thanks for the reply on the ADDH. i would rather not medicate him

anyway unless it becomes a real problem with his schooling later on.

but i'll look up that web site. i have an iep meeting this week with

our elementry school. we are going to put him in their preschool

program 3x a week and other 2 days he is already in a program but he

needs the structure and routine of everyday i believe and so does

his ped. dr and the child study team coordinator. hopefully this

will help him. it is 2 1/2 hrs a day. thanks again.

jodie

(nicholas-5 nonrss, christopher-3 rss 22lbs 33 " , johnathon-6 m

nonrss)

ps- congrates ahead of time on baby #3, and from one busy mom of

three to another to be-make sure to some how have a 10 min break to

your self!!

---

In RSS-Support , " Kacey171 " wrote:

> First of all, I'd like to wish everyone a Happy New Year. I may

be cheating in my reply,

> but it is easier for me to address multiple people in 1 posting,

so I hope this doesn't

> offend anyone!

>

> Congratulations EMILY on your new addition. I too, will be

joining you very soon in

> becoming a mom of 3 (although I think you have your hands fuller

than me with

> young twins & a newborn!)

>

> DANIELLE, my 10 year-old son used to have very significant issue

with sensory

> integration dysfunction, so muh so that he would either vomit at

the sight of things

> that bothered him or turning blue & needing oxygen. You indicated

that Coby has

> always had small sensory issues that you didn't think were

necessary to address. The

> issues of touching grass, sand, rice, etc. may be indicators of

sensory integration

> dysfunction & should be addressed either by an OT or you can do

some activities with

> Coby yourself to help him with this. There are other things that

may indicate a more

> serious sensory problem such as inability to eat or touch certain

textures of food, not

> liking to wear certain clothing fabrics or any clothes at all, not

liking to be hugged or

> cuddled, not liking to get dirty, unable to adjust to hot or cold

temperatures, not

> getting dizzy when most people would, & the list goes on... As

much as any of these

> activitites may make him scream, repetition & time does break kids

of sensory

> disorders. If Coby has difficulty with any of the things I

mentioned above, you can do

> some of the following activities with him: brushing his body with

a soft bristle brush

> (like the ones they use in hospitals to scrub before entering the

operating room), lots

> of spinning and swinging activities on the playground, encouraging

him to walk

> barefoot in sand and grass, playing with messy things such as

finger painting,

> shaving cream, play-doh, dirt, glue, etc., having him help you in

cooking activities in

> which he has to touch messy or sticky ingredients such as peanut

butter, melted

> marshmallow (as in rice krispy treats), cookie dough, and playing

with rice and dry

> beans. After years of therapy with my son, his sensory issues are

minimal if any now.

> My son had years of OT to alleviate this problem among others. He

has never had an

> issue with bathing that I can recall, but he still freaks out a

little in the shower when

> the water is coming down over his head.

>

> SONIA, you asked about your son reaching certain milestones, being

a RSS child. My

> experience was that all gross motor milestones were pretty

delayed. I am not sure if

> this is true for all RSS babies, but when my son was a baby, his

head appeared much

> bigger than the rest of his body. This made it hard for him to be

able to sit up &

> support the weight of his head until he " grew into it " . He also

had weak muscle tone.

> He had & still has dimples in his shoulder blades. I am not sure

if this has to do with

> muscle tone, strength, etc. but I think it also may have been a

factor in upper body

> strength. I like to equate my son's milestones not with his age,

but with his size. He

> sat up, rolled over, walked, etc. when he was the height/weight

of typical children

> that reach those milestones. For example, he was 28 months when

he walked, and at

> that age he was the size of a typical 9-12 month old (the age when

most kids walk).

> Try not to get too stressed about any developmental delays

may encounter. If

> you are doing therapy with him, you are doing all you can & he

will eventually catch

> up to his peers.

>

> MARY, I loved your post about being a parent to a RSS child. What

a great outlook &

> sense of humor you have!

>

> I am not sure who originally addressed the nighttime bed wetting.

Fortunately I didn't

> encounter this problem with either of my children, although

(RSS) potty-

> trained a bit later than the norm. However, I just thought I'd

share that I was at the

> park last week with a friend of mine & she has an 8 year-old & a

six-year-old boy

> who both still wear pull-ups at night. Her oldest son, who is 9,

doesn't have this

> problem. Her children are normal & I consider her to be a super

mom! Just goes to

> show you that there are lots of other parents out there dealing

with the same issue,

> RSS or not. Maybe this isn't just a RSS thing????

>

> Last, but not least, JODIE, my son has ADHD & has taken medication

for this off & on

> since he was 7-years-old. This is hard to diagnose in a young

child & usually

> becomes more of an issue when a child is in grade school. Most of

the medications

> used to treat ADHD are stimulants (controlled substances),

although there is one that

> has been on the market for about a year or so that is not a

stimulant (Strattera). You

> can probably find a website somewhere using a search engine that

has a parent

> questionnaire you can fill out to see if your child is likely to

have ADHD, but even is

> you think he does, the chances of getting him on medication at

such a young age

> would be slim.

>

> I apologize again for my long post, but I hope my replies were

helpful...

>

> Kim (mom to , 10, RSS, , 3, and baby-to-be in

February)

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