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Wow, great information - as we are still on the waiting list for getting therapy

help from the school district and state, I really want to start something to

help my ds's communication first: he already derived a couple of his own sign

language, and knows to give us a picture cue for what he wants. Guess I will

investigate more on both fields, to help him better.

Thanks for the tips.

Re: newbie here

My dd picked up sign language so easily but had no interest in PECS

(pictures) A really cool idea with learning sign language with kids is

videos we

have _www.signingtime.com_ (http://www.signingtime.com) tapes and my girl

loves em! She uses over 125 signs now! She actually out learned a speech

therapist so we had to get her another. Shes almost 4 1/2 and still not

talking so the signs are important. The teachers in her class play the tapes

for

all the kids to learn and they all love em! Even those that are vocal can

learn this second language! Its not difficult just different. Most make

sense, the signs that is. And remember most of our kids arent exact with

their

hand movements so they sign but not perfectly but its amazing to have a

conversation with ur child and it not being vocal. Like at the stores I can

tell her to stop or no or put that down or something and I dont have to say

it

a hundred time and other parents look at me wondering why I cant control my

child instead they are amazed that she knows sign language and wish want to

teach their kids too!! btw I am in no way connected to signing time or

make

anything from referring peeps there.

The PECS board we made ourselves. We just used a polariod camera and took

pictures of the basics to start and stuck them on a board in the main room

so

she could come pull them off and show me. Guess it just took work for her

to walk over and look thru the pictures to find what she wants.

Good luck!!!!!!

*~*~*~*~*~*~*~*

Lena

*~*~*~*~*~*~*~*

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> You know- a lady that i met recently asked my about yeast when she

saw mason scratching in his diaper area.

This is a common sign of yeast overgrowth

http://www.danasview.net/yeast.htm

> I bought the enzymes this morning.the AFP and no Phenol. i am

hopeful that this is the right path for us. does i start him on a full

dose... work my way up to a dose? what IS the dose i give to a baby?

I would start with 1/4 capsule of ONE of the enzymes. Work up to

maybe 1/2 capsule, then start 1/4 capsule of the other one and work up

to 1/2 capsule.

> you mentioned a die off reaction? how will i know? will he get sick

to his stomach?

Sometimes. It depends on how much enzyme you use, and what foods

cause him problems. No-Fenol can also help with yeast.

> i have removed him from dairy once, but i put him back on.... how

lond does it typically take to see a difference?

About 3 days, provided that he is not eating OTHER foods that also

cause problems. Milk and wheat intolerance are commonly seen together.

>>easy would be to take pictures of everything he may think to ask

for. Write them all down first so you remember each. Take pictures

of everything from his favorite cup to him giving you a hug. That way

he can give you a picture of what he wants. You can glue a magnet to

each and put them on the fridge or just put them somewhere he can get

to them. This is a simplified PECS program that is commonly used with

any kids who are non verbal.

I started with this sort of PECS system. It theoretically works well,

but my son was so low functioning he did not understand that a picture

could be a representation of an object. However, this type of system

works well for most non-verbal kids.

>>I know the P is for picture and the E is for exchange, can't

remember the other two letters though!

Picture exchange communication system.

Dana

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>

> the accupuncturist i see recommended we all be tested for toxicity-

but she never specified any thing.

> about the viral aspect, my oldest child has viral problems. (she has

chronic shingles and took valtrex for a short time) .

The coconut oil mentioned previously can be very helpful for this.

I used olive leaf extract for virus issues for my kids, it took about

a year.

> which tests do you specifically recommend through Great Smokies

Diagnostic Laboratory?

The only lab I know of for viral panels is Immunosciences Lab. But

you might contact Great Smokies and see what panels are available there

http://www.gsdl.com/

Dana

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>Eczema is commonly caused by food intolerance. Sometimes enzymes

>help, sometimes not.

My adopted son has eczema also. It is on his cheeks, arms and legs

(basically any body part that shows when he is wearing shorts and a tank

top. It became more noticable when we started him on the 3 HN enzymes, but

I assumed it was because he was having yeast die-off. He has been on the

enzymes for well over a month now but the eczema isn't getting any better.

Should I wait longer or try something different?

Theresa

" We can do no great things; only small things with great love "

~Mother ~

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I would try removing egg for four days and see if it improves. Also,

cod liver oil (Kirkman's 800-245-8282) helps most children.

Lynn

> >Eczema is commonly caused by food intolerance. Sometimes enzymes

> >help, sometimes not.

>

> My adopted son has eczema also. It is on his cheeks, arms and legs

> (basically any body part that shows when he is wearing shorts and a

tank

> top. It became more noticable when we started him on the 3 HN

enzymes, but

> I assumed it was because he was having yeast die-off. He has been

on the

> enzymes for well over a month now but the eczema isn't getting any

better.

> Should I wait longer or try something different?

>

> Theresa

>

> " We can do no great things; only small things with great love "

> ~Mother ~

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>>It became more noticable when we started him on the 3 HN enzymes,

This can be for 3 reasons:

1. Enzyme adjustment period, typically 3 weeks.

2. Does not tolerate one or more of the enzymes. Check the labels

for papain and/or bromelain, they are the ingredients that are

commonly not tolerated.

3. Still eating foods not tolerated, that the enzymes don't address.

Dana

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>I would try removing egg for four days and see if it improves. Also,

>cod liver oil (Kirkman's 800-245-8282) helps most children.

He is tube fed so gets exactly the same food day-in and day-out. He has

always had eczema, could this mean he has always had an intolerance for

something in Pediasure? The eczema was hardly noticeable until we started

the HN enzymes. It still isn't real bad, but is more noticible visually

only. He doesn't scratch or anything at it.

I could try the cod liver oil to see if that will help.

Thanks!

Theresa

" We can do no great things; only small things with great love "

~Mother ~

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> He is tube fed so gets exactly the same food day-in and day-out. He

has

> always had eczema, could this mean he has always had an intolerance for

> something in Pediasure?

Yes.

Dana

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  • 4 months later...

Hi Carolyn,

Welcome to the group! Thanks for the intro. :-) How is PJ adjusting

to his new band? Has your son ever been checked for torticollis?

Torticollis is a tight neck muscle, you can learn more about it here:

http://www.pedisurg.com/PtEduc/Torticollis.htm

http://www.drhull.com/EncyMaster/T/torticollis.html

I ask that b/c you say he favors one side, that's one indication of

tort. Plagio and tort go hand in hand.

I hope you'll post pics of your little cutie. Keep us posted on his

progress.

--- In Plagiocephaly , " Carolyn " <ginasmomma@y...>

wrote:

>

> Hi Everyone,

> My name is Carolyn and we are from New Jersey. I have just

> had my 9 month old son PJ fitted for the band at CT in Paramus. He

> gets the band on TMonday. After many months of debate we have

> decided to go ahead with it. I know some think us crazy b/c he is

> not really severe and he had a head of hair that covers alot of

it.

> In nine months he has had 4 haircuts. Others may not notice but i

> do and figured that if i am going to do i had better do it now. I

> would hate to not do it and regret it later in life.

> My son had dermititis so we had to keep him on his back b/c it

would

> irritate his face if he was on his stomach so he tended and tends

to

> favor one side. He also had a fractured collar bone caused at

birth

> and found out months later.

> Well of course our insurance company (USFHP) for military

families,

> is the worst insurance company i have ever had, has denied the

claim

> saying its cosmetic. I have appealed and it is wherever it is

being

> decided. No doubt the cheap sons of guns will deny it and i will

> have to go further but i will do what i have to do.

> How is that for a long introduction. Hope to talk to some of you

> guys soon.

> Carolyn

>

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Wlcome Carolyn. I'm also from NJ. I live in Robbinsville in Mercer

County not far from you. Good luck with the band. You are in good

hands on this board. Debbie and Brielle

-- In Plagiocephaly , " Carolyn " <ginasmomma@y...>

wrote:

>

> Hi Everyone,

> My name is Carolyn and we are from New Jersey. I have just

> had my 9 month old son PJ fitted for the band at CT in Paramus. He

> gets the band on TMonday. After many months of debate we have

> decided to go ahead with it. I know some think us crazy b/c he is

> not really severe and he had a head of hair that covers alot of

it.

> In nine months he has had 4 haircuts. Others may not notice but i

> do and figured that if i am going to do i had better do it now. I

> would hate to not do it and regret it later in life.

> My son had dermititis so we had to keep him on his back b/c it

would

> irritate his face if he was on his stomach so he tended and tends

to

> favor one side. He also had a fractured collar bone caused at

birth

> and found out months later.

> Well of course our insurance company (USFHP) for military

families,

> is the worst insurance company i have ever had, has denied the

claim

> saying its cosmetic. I have appealed and it is wherever it is

being

> decided. No doubt the cheap sons of guns will deny it and i will

> have to go further but i will do what i have to do.

> How is that for a long introduction. Hope to talk to some of you

> guys soon.

> Carolyn

>

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Hi Carolyn,

Welcome to the group! I hope that your insurance comes through for

you, the bands have been covered for some military families, fight

the good fight! We look forward to hearing from you.

Natasha

Atlanta, GA

--- In Plagiocephaly , " Carolyn " <ginasmomma@y...>

wrote:

>

> Hi Everyone,

> My name is Carolyn and we are from New Jersey. I have

just

> had my 9 month old son PJ fitted for the band at CT in Paramus.

He

> gets the band on TMonday. After many months of debate we have

> decided to go ahead with it. I know some think us crazy b/c he is

> not really severe and he had a head of hair that covers alot of

it.

> In nine months he has had 4 haircuts. Others may not notice but i

> do and figured that if i am going to do i had better do it now. I

> would hate to not do it and regret it later in life.

> My son had dermititis so we had to keep him on his back b/c it

would

> irritate his face if he was on his stomach so he tended and tends

to

> favor one side. He also had a fractured collar bone caused at

birth

> and found out months later.

> Well of course our insurance company (USFHP) for military

families,

> is the worst insurance company i have ever had, has denied the

claim

> saying its cosmetic. I have appealed and it is wherever it is

being

> decided. No doubt the cheap sons of guns will deny it and i will

> have to go further but i will do what i have to do.

> How is that for a long introduction. Hope to talk to some of you

> guys soon.

> Carolyn

>

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Hi Carolyn,

Welcome to the group! I hope that your insurance comes through for

you, the bands have been covered for some military families, fight

the good fight! We look forward to hearing from you.

Natasha

Atlanta, GA

--- In Plagiocephaly , " Carolyn " <ginasmomma@y...>

wrote:

>

> Hi Everyone,

> My name is Carolyn and we are from New Jersey. I have

just

> had my 9 month old son PJ fitted for the band at CT in Paramus.

He

> gets the band on TMonday. After many months of debate we have

> decided to go ahead with it. I know some think us crazy b/c he is

> not really severe and he had a head of hair that covers alot of

it.

> In nine months he has had 4 haircuts. Others may not notice but i

> do and figured that if i am going to do i had better do it now. I

> would hate to not do it and regret it later in life.

> My son had dermititis so we had to keep him on his back b/c it

would

> irritate his face if he was on his stomach so he tended and tends

to

> favor one side. He also had a fractured collar bone caused at

birth

> and found out months later.

> Well of course our insurance company (USFHP) for military

families,

> is the worst insurance company i have ever had, has denied the

claim

> saying its cosmetic. I have appealed and it is wherever it is

being

> decided. No doubt the cheap sons of guns will deny it and i will

> have to go further but i will do what i have to do.

> How is that for a long introduction. Hope to talk to some of you

> guys soon.

> Carolyn

>

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Carolyn,

Welcome. We also used CT(Va.) and had wonderful results. You can see

my Dominicks progress pics on his website

www.mybandedbaby.typepad.com for inspiration,lol. They performed

miracles for us. Keep us posted on how things go with PJ.

CAROLG

--- In Plagiocephaly , " Carolyn " <ginasmomma@y...>

wrote:

>

> Hi Everyone,

> My name is Carolyn and we are from New Jersey. I have just

> had my 9 month old son PJ fitted for the band at CT in Paramus. He

> gets the band on TMonday. After many months of debate we have

> decided to go ahead with it. I know some think us crazy b/c he is

> not really severe and he had a head of hair that covers alot of

it.

> In nine months he has had 4 haircuts. Others may not notice but i

> do and figured that if i am going to do i had better do it now. I

> would hate to not do it and regret it later in life.

> My son had dermititis so we had to keep him on his back b/c it

would

> irritate his face if he was on his stomach so he tended and tends

to

> favor one side. He also had a fractured collar bone caused at

birth

> and found out months later.

> Well of course our insurance company (USFHP) for military

families,

> is the worst insurance company i have ever had, has denied the

claim

> saying its cosmetic. I have appealed and it is wherever it is

being

> decided. No doubt the cheap sons of guns will deny it and i will

> have to go further but i will do what i have to do.

> How is that for a long introduction. Hope to talk to some of you

> guys soon.

> Carolyn

>

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Carolyn,

Welcome. We also used CT(Va.) and had wonderful results. You can see

my Dominicks progress pics on his website

www.mybandedbaby.typepad.com for inspiration,lol. They performed

miracles for us. Keep us posted on how things go with PJ.

CAROLG

--- In Plagiocephaly , " Carolyn " <ginasmomma@y...>

wrote:

>

> Hi Everyone,

> My name is Carolyn and we are from New Jersey. I have just

> had my 9 month old son PJ fitted for the band at CT in Paramus. He

> gets the band on TMonday. After many months of debate we have

> decided to go ahead with it. I know some think us crazy b/c he is

> not really severe and he had a head of hair that covers alot of

it.

> In nine months he has had 4 haircuts. Others may not notice but i

> do and figured that if i am going to do i had better do it now. I

> would hate to not do it and regret it later in life.

> My son had dermititis so we had to keep him on his back b/c it

would

> irritate his face if he was on his stomach so he tended and tends

to

> favor one side. He also had a fractured collar bone caused at

birth

> and found out months later.

> Well of course our insurance company (USFHP) for military

families,

> is the worst insurance company i have ever had, has denied the

claim

> saying its cosmetic. I have appealed and it is wherever it is

being

> decided. No doubt the cheap sons of guns will deny it and i will

> have to go further but i will do what i have to do.

> How is that for a long introduction. Hope to talk to some of you

> guys soon.

> Carolyn

>

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Hi Carolyn,

I just wanted to post to welcome you to the group! We seem to have

several new members from the New Jersey area here recently, so

that's wonderful... it's always helpful to have others around from

your general area who can give feedback on facilities or suggestions

about travel and so forth.

Would you keep us posted on how PJ's initial fitting goes? I hope

you all have a great visit!

Take care,

Christie (Mom to Repo'd Remy)

--- In Plagiocephaly , " Carolyn " <ginasmomma@y...>

wrote:

>

> Hi Everyone,

> My name is Carolyn and we are from New Jersey. I have

just

> had my 9 month old son PJ fitted for the band at CT in Paramus.

He

> gets the band on TMonday. After many months of debate we have

> decided to go ahead with it. I know some think us crazy b/c he is

> not really severe and he had a head of hair that covers alot of

it.

> In nine months he has had 4 haircuts. Others may not notice but i

> do and figured that if i am going to do i had better do it now. I

> would hate to not do it and regret it later in life.

> My son had dermititis so we had to keep him on his back b/c it

would

> irritate his face if he was on his stomach so he tended and tends

to

> favor one side. He also had a fractured collar bone caused at

birth

> and found out months later.

> Well of course our insurance company (USFHP) for military

families,

> is the worst insurance company i have ever had, has denied the

claim

> saying its cosmetic. I have appealed and it is wherever it is

being

> decided. No doubt the cheap sons of guns will deny it and i will

> have to go further but i will do what i have to do.

> How is that for a long introduction. Hope to talk to some of you

> guys soon.

> Carolyn

>

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Hi Carolyn,

I just wanted to post to welcome you to the group! We seem to have

several new members from the New Jersey area here recently, so

that's wonderful... it's always helpful to have others around from

your general area who can give feedback on facilities or suggestions

about travel and so forth.

Would you keep us posted on how PJ's initial fitting goes? I hope

you all have a great visit!

Take care,

Christie (Mom to Repo'd Remy)

--- In Plagiocephaly , " Carolyn " <ginasmomma@y...>

wrote:

>

> Hi Everyone,

> My name is Carolyn and we are from New Jersey. I have

just

> had my 9 month old son PJ fitted for the band at CT in Paramus.

He

> gets the band on TMonday. After many months of debate we have

> decided to go ahead with it. I know some think us crazy b/c he is

> not really severe and he had a head of hair that covers alot of

it.

> In nine months he has had 4 haircuts. Others may not notice but i

> do and figured that if i am going to do i had better do it now. I

> would hate to not do it and regret it later in life.

> My son had dermititis so we had to keep him on his back b/c it

would

> irritate his face if he was on his stomach so he tended and tends

to

> favor one side. He also had a fractured collar bone caused at

birth

> and found out months later.

> Well of course our insurance company (USFHP) for military

families,

> is the worst insurance company i have ever had, has denied the

claim

> saying its cosmetic. I have appealed and it is wherever it is

being

> decided. No doubt the cheap sons of guns will deny it and i will

> have to go further but i will do what i have to do.

> How is that for a long introduction. Hope to talk to some of you

> guys soon.

> Carolyn

>

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Carolyn,

Good luck tomorrow!

You won't regret the decision. Our 4 year old son was banded from 5-

8 months of age. He was on the severe side but got amazing

correction. Our new pediatrician doesn't believe he had anything

wrong with him since he looks so great!

Our newest addition, Cecelia, started getting flat this summer.

Instead of getting better it was getting worse as she aged. She so

also got a DOC Band two weeks ago. Just like PJ she's 9 months

old!

Her plagio is not nearly as bad a Dane's was but we felt that we had

to take it seriously. Having been down this path before we knew the

DOC Band wouldn't bother her and could only help her. At her age we

figured we could only regret not banding her.

She had her first adjustment on Friday. I was a little worried she

wouldn't get the awesome correction Dane got because she is older

but I'm happy to say that she is looking much rounder already.

I'm so sorry to hear about your insurance. This is not uncommon

even for civilian families. Fight like hell. You deserve every

cent.

Mom to Dane 4 yo (DOC Grad) and Cecelia 9 months (DOC Band 09/05)

--- In Plagiocephaly , " Carolyn " <ginasmomma@y...>

wrote:

>

> Hi Everyone,

> My name is Carolyn and we are from New Jersey. I have

just

> had my 9 month old son PJ fitted for the band at CT in Paramus.

He

> gets the band on TMonday. After many months of debate we have

> decided to go ahead with it. I know some think us crazy b/c he is

> not really severe and he had a head of hair that covers alot of

it.

> In nine months he has had 4 haircuts. Others may not notice but i

> do and figured that if i am going to do i had better do it now. I

> would hate to not do it and regret it later in life.

> My son had dermititis so we had to keep him on his back b/c it

would

> irritate his face if he was on his stomach so he tended and tends

to

> favor one side. He also had a fractured collar bone caused at

birth

> and found out months later.

> Well of course our insurance company (USFHP) for military

families,

> is the worst insurance company i have ever had, has denied the

claim

> saying its cosmetic. I have appealed and it is wherever it is

being

> decided. No doubt the cheap sons of guns will deny it and i will

> have to go further but i will do what i have to do.

> How is that for a long introduction. Hope to talk to some of you

> guys soon.

> Carolyn

>

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Carolyn,

Good luck tomorrow!

You won't regret the decision. Our 4 year old son was banded from 5-

8 months of age. He was on the severe side but got amazing

correction. Our new pediatrician doesn't believe he had anything

wrong with him since he looks so great!

Our newest addition, Cecelia, started getting flat this summer.

Instead of getting better it was getting worse as she aged. She so

also got a DOC Band two weeks ago. Just like PJ she's 9 months

old!

Her plagio is not nearly as bad a Dane's was but we felt that we had

to take it seriously. Having been down this path before we knew the

DOC Band wouldn't bother her and could only help her. At her age we

figured we could only regret not banding her.

She had her first adjustment on Friday. I was a little worried she

wouldn't get the awesome correction Dane got because she is older

but I'm happy to say that she is looking much rounder already.

I'm so sorry to hear about your insurance. This is not uncommon

even for civilian families. Fight like hell. You deserve every

cent.

Mom to Dane 4 yo (DOC Grad) and Cecelia 9 months (DOC Band 09/05)

--- In Plagiocephaly , " Carolyn " <ginasmomma@y...>

wrote:

>

> Hi Everyone,

> My name is Carolyn and we are from New Jersey. I have

just

> had my 9 month old son PJ fitted for the band at CT in Paramus.

He

> gets the band on TMonday. After many months of debate we have

> decided to go ahead with it. I know some think us crazy b/c he is

> not really severe and he had a head of hair that covers alot of

it.

> In nine months he has had 4 haircuts. Others may not notice but i

> do and figured that if i am going to do i had better do it now. I

> would hate to not do it and regret it later in life.

> My son had dermititis so we had to keep him on his back b/c it

would

> irritate his face if he was on his stomach so he tended and tends

to

> favor one side. He also had a fractured collar bone caused at

birth

> and found out months later.

> Well of course our insurance company (USFHP) for military

families,

> is the worst insurance company i have ever had, has denied the

claim

> saying its cosmetic. I have appealed and it is wherever it is

being

> decided. No doubt the cheap sons of guns will deny it and i will

> have to go further but i will do what i have to do.

> How is that for a long introduction. Hope to talk to some of you

> guys soon.

> Carolyn

>

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Hi Jen...I was in my late 20's when I was dx'd with sero-negative lupus and

mixed connective tissue disease. In my thirties I was dx'd with chronic fatigue

syndrome, then fibromyalgia. In my forties I was dx'd with rheumatoid

arthritis, psoriatic arthritis and sjogren's syndrome. I, too, am not sure

" what " exactly I have...I call it " autoimmune potpourri " though my doctors are

settled on Ra, PsA, FMS and Sjogren's. My children were very small when I was

first dx'd. All this to say I do understand your situation, and I am glad you

are here to receive all the good blessings from this great groups of fellow

survivors.

Hugs...

Tess in Oregon

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Hi Tess,

Thanks for the welcome! My PM doctor suggested that maybe I have some

sort of mixed connective tissue disorder, but when I read about it, I

really don't have any of the diseases that meet that criteria. It's

just kinda frustrating going ahead into the unknown....which I'm sure

you know well. My girls were older, 9 and 11, when I started getting

sick, so they unfortunately got to see me change right before their

eyes. That was hard. I'm glad I'm here too...this feels like a very

good group!

Jen

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  • 10 months later...

Just curious. How is she socially?

As a young girl, I played with my neighbors (as long as it was star

wars, and I guess played by my rules) and Didn't have friends at

school in elementary.

How about routine or structure?

Does she socialize with kids her age, adults, younger kids?

Does she collect something at all or talk a lot about certain subjects

she likes?

Just curious. These are just a sample of things that an Aspie " could "

do, and I wonder if she does any of that.

*smiles*

b

>

> Some people are questioning whether my daughter has AS. She has not

> even been looked at and I do not know if this is a route I should

> take. About 1.5 yrs ago she was diagnosed ADHD & CAPD. I have always

> thought we still were missing something. She is doing lots better in

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Yes, now she even sounds more like me when I was little.

veeerrryy interesting, and worthwhile, in my opinion to work with

her and help her like she actually got the diagnosis.

Dad, well, for some dads, they are a whole other story.

I think she is fine too, just perhaps 'differen't' on some things.

(and that justs might be Asperger Syndrome!!)

*smiles*

lisa b

>

> She has a rock collection that she also collects at school. Says

she does not really play with anyone at school, just roams around by

herself. My girlfriends daughter her age (9) says she is crazy and

gets aggitated with her. At school things are pretty routine at home

I would say somewhat routine, but she still has to be reminded

everyday about her list of things to be done. Like brush teeth,

hair, dry hair etc...

> She seems to associate with younger kids like they are more her

speed sometimes.

>

> My husband thinks everything is just fine.

>

>

>

>

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Well, you should probably investigate why she is having these problems. They

all seem related to sensory problems.

Roxanna

( ) Newbie Here

Some people are questioning whether my daughter has AS. She has not

even been looked at and I do not know if this is a route I should

take. About 1.5 yrs ago she was diagnosed ADHD & CAPD. I have always

thought we still were missing something. She is doing lots better in

school with Concerta and being at a new school. They have a smaller

class size and she is in an inclusive class. She is in 4th grade. She

has not even gone to SPED this year because her teacher feels she is

staying on tract quite well. Her issues that these people are looking

at are:

She can not stand being at the peprally, they do not have a band just

a lot of screaming kids and loud music on the PA.

She has issues with being on the bus due to the loud noise

She has issues with her socks they have to be put on 100% right (the

line over the toes)

She will not wear tight fitting shirts (around the arms)

She is real sensitive to light, like going to the eye doc or a really

suny day (she has fair skin, blond hair, blue eyes)

Tasks have to be given to her 1-2 at a time, I can not roll out a

list unless it is written

She has even told her teacher that she might need to be moved to

another class because it is too loud in there.

She is exceptionally wonderful in art!

This is just a small run down

Any thoughts appreciated

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  • 6 months later...
Guest guest

Hi, welcome!

jacklyn <sunkissable36@...> wrote:

hello everyone,im glad i found this group!i'm a single mother of an

almost 3 year old boy.he's also a late talker/ speech delay.and i look

forward to meeting new people that are going thru the same,because i

know how frustrating it can be at times and talking to others going

thru the same thing would be so nice...thanks

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Guest guest

> hello everyone,im glad i found this group!i'm a single

mother of an

> almost 3 year old boy.he's also a late talker/ speech delay.and i

look

> forward to meeting new people that are going thru the same,because

i

> know how frustrating it can be at times and talking to others

going

> thru the same thing would be so nice...thanks

>

> -------------------------------------------------------------------

hello and welcome jacklyn,

I too have a lil boy with speech delay. My son was diagnosed

with verbal apraxia about a year ago. I can truely relate to your

frustrations.

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

>

>

>

>

>

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