Hello Everyone

[Guest guest]

Wow, that must depend where you live. My internet has never gone out

in the 5 years I have lived here.

> >

> > > Internet does not go out in the rain...whether phone or dsl...? I

> > >

> > Satalite-based internet might...

> >

> > Jim

> >

> >

>

[Guest guest]

Do you have satellite? If you don't then it doesn't affect you.

Satellite internet goes out. It has nothing to do with cable or dsl or

modem internet. Another animal. If you do have satellite, you must have

a great angle on it.

Jada wrote:

>

> Wow, that must depend where you live. My internet has never gone out

> in the 5 years I have lived here.

>

>

> > >

> > > > Internet does not go out in the rain...whether phone or dsl...? I

> > > >

> > > Satalite-based internet might...

> > >

> > > Jim

> > >

> > >

> >

>

>

[Guest guest]

You can post a picture of her and let us take a look.

In some case, it is true that it will round up a

little in mild case.

--- edandambere <edandambere@...> wrote:

> I was wondering if anyone here had a child with the

> mild Plagiocephaly?

> I went to 3 Peds and now my daughter is 13 months

> and they want do

> nothing to help her. I even went to the extreme and

> took her to a

> Craniologist and the basically laughed at me and

> said that her's was so

> mild that her hair would cover it up in time but, to

> me I notice every

> time I look at her but, it's only on the back of her

> head and she does

> have alot of hair but, they said that it might round

> out more has

> anyone had this happen to them and if so what was

> the outcome of it?

> Thanks everyone just really upset:(

>

>

________________________________________________________________________________\

____

Never miss a thing. Make your home page.

http://www./r/hs

[Guest guest]

Hello

Any chance this sort of post could be refused please? its off topic

and the person should be redirected to a more suitable forum such as

aspievillage.

Before i reply to this person, is this a scam?

--

is

[Guest guest]

This message appears here every month or so. The individual does not reply to

e-mail either posted on this list or sent individually. I don't know whether

it's a scam or not, but it does seem to be a waste of time.

S S

Re: Hello Everyone

Posted by: " is " alexis.atrekkie22@... atrekkie22

Sat May 3, 2008 2:35 pm (PDT)

Hello

Any chance this sort of post could be refused please? its off topic

and the person should be redirected to a more suitable forum such as

aspievillage.

Before i reply to this person, is this a scam?

--

is

_______________________________________________

Join Excite! - http://www.excite.com

The most personalized portal on the Web!

[Guest guest]

I just did mine for the 2nd time......i actually hadda perdy good time this time

as everyone was really cool. We all just chit chatted the whole time which made

it alot faster and easier.....sometimes my black cloud backs off, lol

Tim

Rock Hard Rock Forever!

[Guest guest]

,

Welcome to the group. I am sorry that your Caleb is going through so much.

I hope you find much support and strength to help him through all of his

struggles., and yours.

I would suggest either signing or a picture book to help him with

communicating.

Kayce

On Mon, Oct 27, 2008 at 5:45 PM, <mlwg81@...> wrote:

> Hello Everyone!

>

> My name is and I am the mother to Caleb. Caleb is 3 years old

> and diagnosed with Wolf Hirschhorn Syndrome which is a deletion of

> chromesome # 4. He was recently said to have Apraxia and we've started

> him on Fish Oil vitamins. I am totally at a loss for all of this simply

> because it is so frustrating. He knows what he wants to tell me but I

> just can't figure it out which intels him getting frustrated and myself

> as well.

>

> Anyone have any tips since all of this is new to me?

>

> Thanks and I look forward to talking with you all!

>

> Gainey

>

>

>

[Guest guest]

Kayce,

Thanks for responding. Caleb is my world and it hurts me tremendously

to see him go through so much in just his 3 short years thus far. His

speech therapist has suggessted getting him the Go Talk communication

board. Have you heard of it? Do you have any experience with it? Or

does anyone for that matter. I am starting to see a minor difference

with using the vitamins but not a major one yet. We have tried sign

language but he has only really picked up 3 of the signs, which have

been more, please, and finished. Other than that it's the guessing

game with him if he doesn't know how to say it.

Thanks again and I look forward to talking with you again!!

>

> > Hello Everyone!

> >

> > My name is and I am the mother to Caleb. Caleb is 3

years old

> > and diagnosed with Wolf Hirschhorn Syndrome which is a deletion of

> > chromesome # 4. He was recently said to have Apraxia and we've

started

> > him on Fish Oil vitamins. I am totally at a loss for all of this

simply

> > because it is so frustrating. He knows what he wants to tell me

but I

> > just can't figure it out which intels him getting frustrated and

myself

> > as well.

> >

> > Anyone have any tips since all of this is new to me?

> >

> > Thanks and I look forward to talking with you all!

> >

> > Gainey

> >

> >

> >

>

>

>

[Guest guest]

I've seen it, haven't personally used it. Cody's SLP has just used board

maker to basically make a picture book. Simple, not complicated, pictures

are always added (for example, halloween things--candy, costume, etc). Have

you tried signing time dvds?

I haven't had any luck with vitamins. I guess it works for some, but not

for all.

Caleb is very lucky to have a strong & determined mother. Be proud of

yourself.

On Tue, Oct 28, 2008 at 7:10 AM, <mlwg81@...> wrote:

> Kayce,

>

> Thanks for responding. Caleb is my world and it hurts me tremendously

> to see him go through so much in just his 3 short years thus far. His

> speech therapist has suggessted getting him the Go Talk communication

> board. Have you heard of it? Do you have any experience with it? Or

> does anyone for that matter. I am starting to see a minor difference

> with using the vitamins but not a major one yet. We have tried sign

> language but he has only really picked up 3 of the signs, which have

> been more, please, and finished. Other than that it's the guessing

> game with him if he doesn't know how to say it.

>

> Thanks again and I look forward to talking with you again!!

>

>

>

>

> >

> > > Hello Everyone!

> > >

> > > My name is and I am the mother to Caleb. Caleb is 3

> years old

> > > and diagnosed with Wolf Hirschhorn Syndrome which is a deletion of

> > > chromesome # 4. He was recently said to have Apraxia and we've

> started

> > > him on Fish Oil vitamins. I am totally at a loss for all of this

> simply

> > > because it is so frustrating. He knows what he wants to tell me

> but I

> > > just can't figure it out which intels him getting frustrated and

> myself

> > > as well.

> > >

> > > Anyone have any tips since all of this is new to me?

> > >

> > > Thanks and I look forward to talking with you all!

> > >

> > > Gainey

> > >

> > >

> > >

> >

> >

> >

[Guest guest]

Hi ,

It is heartbreaking to watch your preschooler have thoughts, ideas, needs,

and be unable to share them. One thing that helped us is signing. Signing

Time dvds is a series, available from www.signingtime.com, or Amazon, or

your local library. They are fun, entertaining dvds that teach signing.

I have made extensive use of our library network, they have a site for the

state, whereby I can access all the libraries in Massachusetts, order the

dvd/book/cd I want, and it gets sent to my local library. We are also in the

process of trying to get our son moved to a preschool for the deaf and hard

of hearing, out of district, where my son would be in an immersive signing

environment. The idea is that signing would provide a reliable back up means

of communication, until he can speak more fluently.

Hope that helps!

Nadine

On Mon, Oct 27, 2008 at 7:29 PM, Kayce Spader <kaycespader@...> wrote:

> ,

> Welcome to the group. I am sorry that your Caleb is going through so much.

> I hope you find much support and strength to help him through all of his

> struggles., and yours.

> I would suggest either signing or a picture book to help him with

> communicating.

>

> Kayce

>

> On Mon, Oct 27, 2008 at 5:45 PM,

<mlwg81@...<mlwg81%40>>

> wrote:

>

> > Hello Everyone!

> >

> > My name is and I am the mother to Caleb. Caleb is 3 years old

> > and diagnosed with Wolf Hirschhorn Syndrome which is a deletion of

> > chromesome # 4. He was recently said to have Apraxia and we've started

> > him on Fish Oil vitamins. I am totally at a loss for all of this simply

> > because it is so frustrating. He knows what he wants to tell me but I

> > just can't figure it out which intels him getting frustrated and myself

> > as well.

> >

> > Anyone have any tips since all of this is new to me?

> >

> > Thanks and I look forward to talking with you all!

> >

> > Gainey

> >

> >

> >

>

>

[Guest guest]

Hi ,

Will (my son) tried the Go Talk, and then a more sophisticated version, that

was a computer with lots of depth, but in the end our SLP recommended we

choose one form of " back up communication " . She felt that it would not have

as much impact to use various forms of augmentative communication, and in

the end, we agreed that focusing on just one seemed to make more sense for

to us.

With Will, he figured out the Go Talk (and computer) quite handily, but we

found it wasn't as organic a form of communication as signing. To have to

go, and get this computer, and the Go Talk only had something like 16

options on it, in the midst of play (he has two older siblings) seemed more

cumbersome than to use his hands. The whole family, though, had to get with

the program, and sign, to encourage his signing. I have to admit, now that

he's saying more, we're being less vigilant on the signing side of things,

and more reliant on the speech. He will be 4 in November.

Obviously, every kid is different, as is every family, but it's great that

there are now options for augmentative communication.

Nadine

On Tue, Oct 28, 2008 at 7:46 AM, Kayce Spader <kaycespader@...> wrote:

> I've seen it, haven't personally used it. Cody's SLP has just used board

> maker to basically make a picture book. Simple, not complicated, pictures

> are always added (for example, halloween things--candy, costume, etc). Have

> you tried signing time dvds?

> I haven't had any luck with vitamins. I guess it works for some, but not

> for all.

> Caleb is very lucky to have a strong & determined mother. Be proud of

> yourself.

>

>

> On Tue, Oct 28, 2008 at 7:10 AM,

<mlwg81@...<mlwg81%40>>

> wrote:

>

> > Kayce,

> >

> > Thanks for responding. Caleb is my world and it hurts me tremendously

> > to see him go through so much in just his 3 short years thus far. His

> > speech therapist has suggessted getting him the Go Talk communication

> > board. Have you heard of it? Do you have any experience with it? Or

> > does anyone for that matter. I am starting to see a minor difference

> > with using the vitamins but not a major one yet. We have tried sign

> > language but he has only really picked up 3 of the signs, which have

> > been more, please, and finished. Other than that it's the guessing

> > game with him if he doesn't know how to say it.

> >

> > Thanks again and I look forward to talking with you again!!

> >

> >

> >

> >

> > >

> > > > Hello Everyone!

> > > >

> > > > My name is and I am the mother to Caleb. Caleb is 3

> > years old

> > > > and diagnosed with Wolf Hirschhorn Syndrome which is a deletion of

> > > > chromesome # 4. He was recently said to have Apraxia and we've

> > started

> > > > him on Fish Oil vitamins. I am totally at a loss for all of this

> > simply

> > > > because it is so frustrating. He knows what he wants to tell me

> > but I

> > > > just can't figure it out which intels him getting frustrated and

> > myself

> > > > as well.

> > > >

> > > > Anyone have any tips since all of this is new to me?

> > > >

> > > > Thanks and I look forward to talking with you all!

> > > >

> > > > Gainey

> > > >

> > > >

> > > >

> > >

> > >

> > >

[Guest guest]

My two year old is the same way, he has global developmental delays, especially

in speech and vocab. I think that my son also knows what he wants to say, but it

doesn't sound the same when he tries to say it. He gets frustrated easily and

that leads to fits and tantrums. We have started making up words for common

items, using sounds that he can easily make. He uses his words to tell us what

he wants and we use our words to tell him what it is when we give it to him. So

far, he has learned the words " juice " " doggie " " eat " and " bye " this way. He is

in the process of learning his brothers name now. He still says gun instead of

Cullen, but we're getting there.

Practice random acts of kindness...

From: <mlwg81@...>

Subject: [ ] Hello Everyone

Date: Monday, October 27, 2008, 5:45 PM

Hello Everyone!

My name is and I am the mother to Caleb. Caleb is 3 years old

and diagnosed with Wolf Hirschhorn Syndrome which is a deletion of

chromesome # 4. He was recently said to have Apraxia and we've started

him on Fish Oil vitamins. I am totally at a loss for all of this simply

because it is so frustrating. He knows what he wants to tell me but I

just can't figure it out which intels him getting frustrated and myself

as well.

Anyone have any tips since all of this is new to me?

Thanks and I look forward to talking with you all!

Gainey

[Guest guest]

Joy and ,

I went for the long awaited appointment with the pediatric neurologist today.

I'm too tired to post what happened (I'll save it for tomorrow) but on the way

to Tulsa I had a few hours to spend with Shyann (she's 8.11 yrs.) just talking

heart to heart, mother to daughter. Shyann's speech is so bad right now and I

can't wait to put her back on oils. She was speaking so much clearer and we

discussed this at length. She told me that when she plans on saying something

she thinks it in her head and it sounds right, then she says it and it comes out

all garbled. She said fish oils helped not only her speech but all aspects of

her thinking. Anyhow, she said that without the oils she went back to how it

always was; think it clear and speak it wrong. I always wondered when she was

three and non-verbal if she thought the right words. But her whole vocabulary

was " guy guy guy " .  So when I read your posts I thought I'd share this with you.

Joy, your two year old

son and , your son Caleb are thinking those words they want to say!

They are bright children who know what they want to express, but are just having

their apraxic moments. But they will learn to talk! I think Shyann's words

answered what you already know; think clear, speak apraxic. Just be patient with

your precious ones because it is so frustrating for them. All I can do is give

you hope that they will soon be able to express their selves, and to validate

(through Shyann) that you are right! (Mothers' usually are!). All the best to

both of you..

Joy and Shyann 

________________________________

From: Joy <tmdj06@...>

Sent: Tuesday, October 28, 2008 1:11:55 PM

Subject: Re: [ ] Hello Everyone

My two year old is the same way, he has global developmental delays, especially

in speech and vocab. I think that my son also knows what he wants to say, but it

doesn't sound the same when he tries to say it. He gets frustrated easily and

that leads to fits and tantrums. We have started making up words for common

items, using sounds that he can easily make. He uses his words to tell us what

he wants and we use our words to tell him what it is when we give it to him. So

far, he has learned the words " juice " " doggie " " eat " and " bye " this way. He is

in the process of learning his brothers name now. He still says gun instead of

Cullen, but we're getting there.

Practice random acts of kindness...

From: <mlwg81 (DOT) com>

Subject: [childrensapraxiane t] Hello Everyone

@groups. com

Date: Monday, October 27, 2008, 5:45 PM

Hello Everyone!

My name is and I am the mother to Caleb. Caleb is 3 years old

and diagnosed with Wolf Hirschhorn Syndrome which is a deletion of

chromesome # 4. He was recently said to have Apraxia and we've started

him on Fish Oil vitamins. I am totally at a loss for all of this simply

because it is so frustrating. He knows what he wants to tell me but I

just can't figure it out which intels him getting frustrated and myself

as well.

Anyone have any tips since all of this is new to me?

Thanks and I look forward to talking with you all!

Gainey

[Guest guest]

Hi! Welcome to our group! I hope you find lots of support and useful

information.

 

I also have spondylolethesis and herniated discs at L4 L5 and S1.

 

My pain is generally in my right calf and not in my back. I look forward to

talking with you more, I can't really type a long one because I am watching

American Idol. I will respond more tomorrow.

Dawn E.

I would rather be hated for who I am

than to be like for who I am not ~Author Unknown

From: mybryanagirl <mybryanagirl@...>

Subject: hello everyone

spinal problems

Date: Tuesday, January 27, 2009, 7:41 PM

I am new to this support group and have read plenty of the emails. Let

me give you a little history on me so that I can catch up.

I am a 40 year old mother of a 22 year old, 21 year old, and 4 year

old and I have a 1 year old grandson. When I was young I was into

sports, horses, dancing, all kinds of things that can really mess your

back up. Anyway, from the time that I was about 13 I started having

lower back pains. I remember being in so much pain and my lower back

having a big swell on it and my mom taking me to the Dr who said to

just have her rest. So years go by and my back still bothered me from

time to time but each doctor would just give me a shot or a

prescription of ibuprofen and send me on my way. It wasn't until I met

my doctor now who said that she would like to know why my back hurt (

imagine that, a doctor who cared) so she sent me in for x-rays then a

mri and found that I had Spondylolethesis. so sure enough I had to

have a fusion with laminectomy in April of 2008. I went back to work a

month and half later and did 1 month of pt. My surgeon has me coming

back this April to see if I am fully fused yet.

So that is my story. Of course I kept out all the pains and things

that I went through.

[Guest guest]

This email is a hoax, it shows up on just about every autism board I have been

too, and some non autism groups. This email address should be banned. Do not

reply to this person, it's probably fishing for email addresses.

>

> I am a female that has Autism the Aspergers kind. I am not feeling good My Job

changed my status to PRN As Needed status. Because of this I am in need of a new

Job and because of my current job my Job coach, group home , Voc Rehab and my

case manager will not help me about getting a new job. I have some questions my

questions are:

> 1. I am in need of a new job because my job status is at PRN As Needed How can

I look for a Job I do not drive or have transportation and need help with

looking for a job?

> 2. Is there anyone that can work with me on looking for a Job

> 3. Is there anyone that can help me with finding some volunteer work?

> 4. I am suppose to be out of my group home between 9:00am-2:00pm either

working or volunteering somewhere every single day is there an agency that can

help me find some volunteer work

> 5. Is there an agency that can help me with looking for a Job because if I go

to Goodwill etc... they tell me to go to Voc Rehab.

>

> If you know the answers please e-mail me at

>

> CHANNING28105@...

> CHANNING28270@...

> CHANCHAN79@...

>

> Channing

>

[Guest guest]

>This email is a hoax, it shows up on just about every autism board I

>have been too, and some non autism groups. This email address should

>be banned. Do not reply to this person, it's probably fishing for

>email addresses.

Actually, despite being the first one to suspect hoaxes with pretty

much everything, I think this one looks legit.

Look here:

http://aspergers.meetup.com/81/members/8245543/

>

>

>>

>> I am a female that has Autism the Aspergers kind. I am not feeling

>>good My Job changed my status to PRN As Needed status. Because of

>>this I am in need of a new Job and because of my current job my Job

>>coach, group home , Voc Rehab and my case manager will not help me

>>about getting a new job. I have some questions my questions are:

>> 1. I am in need of a new job because my job status is at PRN As

>>Needed How can I look for a Job I do not drive or have

>>transportation and need help with looking for a job?

>> 2. Is there anyone that can work with me on looking for a Job

>> 3. Is there anyone that can help me with finding some volunteer work?

>> 4. I am suppose to be out of my group home between 9:00am-2:00pm

>>either working or volunteering somewhere every single day is there

>>an agency that can help me find some volunteer work

>> 5. Is there an agency that can help me with looking for a Job

>>because if I go to Goodwill etc... they tell me to go to Voc Rehab.

>>

>> If you know the answers please e-mail me at

>>

>> CHANNING28105@...

>> CHANNING28270@...

>> CHANCHAN79@...

>>

>> Channing

>>

>

>

>

--

Ralph Nader on the need for moral courage:

[Guest guest]

Channing Ashbaugh wrote:

> How can my Rash that is on the skin under my tummy near my legs which reoccurs

cause me to have a yeast infection that shows up in any urine specimen because I

have been told by doctors that the rash under my tummy is both fungus and Yeast.

Does anyone have this that can relate to me with this?

>

I have no help to offer, but I have had such a rash, only on one side of

my stomach, at the top of my leg. Very weird, and nothing I put on it

seemed to help much, but 1% hydrocortisone cream helped better than

other things I tried. At the time I thought it was a flare of chronic

dermatitis, but it was not itching, nor did it blister like eczema, nor

was it bumpy like hives. Eventually it went away after many weeks, and I

never had it looked at.

sol

[Guest guest]

Yeast can be systemic (that is what candidiasis is, systemic yeast. The rash is

a symptom of yeast in your system, it's not CAUSING the yeast showing up in your

urine. A lot of yeast is often in the intestine but it can be in other places

too.

Vicky

> > How can my Rash that is on the skin under my tummy near my legs which

reoccurs cause me to have a yeast infection that shows up in any urine specimen

because I have been told by doctors that the rash under my tummy is both fungus

and Yeast. Does anyone have this that can relate to me with this?

> >

>

[Guest guest]

Have you tried any sensory strategies or sensory diet? Some examples below...please seek the advise of a certifed occupational therapist before instituting a therapeutic sensory diet. Pam

Heavy Work Activities

In a message dated 4/27/2009 6:36:18 P.M. Eastern Daylight Time, betsymaye36@... writes:

Hi I am new to the group, I have a 8yrd daughter .She was diagnosed with PDD in kindergarten . I was able to get her in a good program and a IEP for school. I just have a question is their any soultions to hyperness ,by ways of no meds . She is on adderall now . It seems to work for school but it dose not carry her through after scholl and evening . Their solution is to give her more medication. Is there any suggestions as to waht I could try with her after school?????

Access 350+ FREE radio stations anytime from anywhere on the web. Get the Radio Toolbar!

[Guest guest]

Great suggestion. Sensory diets can help a bunch!

"Over-optimism is waiting for you ship to come in when you haven't sent one out."

From: "ppanda65@..." <ppanda65@...> Sent: Monday, April 27, 2009 6:31:17 PMSubject: Re: ( ) Hello everyone

Have you tried any sensory strategies or sensory diet? Some examples below...please seek the advise of a certifed occupational therapist before instituting a therapeutic sensory diet. Pam

Heavy Work Activities

In a message dated 4/27/2009 6:36:18 P.M. Eastern Daylight Time, betsymaye36 writes:

Hi I am new to the group, I have a 8yrd daughter .She was diagnosed with PDD in kindergarten . I was able to get her in a good program and a IEP for school. I just have a question is their any soultions to hyperness ,by ways of no meds . She is on adderall now . It seems to work for school but it dose not carry her through after scholl and evening . Their solution is to give her more medication. Is there any suggestions as to waht I could try with her after school?????

Access 350+ FREE radio stations anytime from anywhere on the web. Get the Radio Toolbar!

[Guest guest]

Hi Charlotte--Here is the name of an advocacy who helped me get services and

better treatment for my son--It's free of charge--see if they can help

you--Missouri Protection & Advocacy--ask for Byron Koster,Senior Advocate, He

greatly helped out my family.

From: Channing Ashbaugh <channing28270@...>

Subject: [ ] Hello Everyone

Date: Thursday, April 30, 2009, 7:10 AM

I am a female with Autism- The Aspergers kind. I live in a group home in

Charlotte, North Carolina. I am not getting any money at all to get haircuts at

all .I cut my own hair recently because I do not get any money for haircuts and

the group home staff yelled at me . I want to get my hair straightened out and

the group home will not let me get a Haircut At All.The Group home is neglecting

the fact I still need haircuts. My Parents also yelled at me because I cut my

hair and is neglecting the fact I still need haircuts. What Can I do? My Job

which is an on Call only Job is not calling me in up to where I am not getting a

Paycheck at all. Any money that I get from the Social Security Administration

and Special Assistance all goes to pay for my Rent up to where I do not get any

money for haircuts. Other Than not getting any money for haircuts I am not

getting any money to get things like:

1.Postage Stamps

2.toiletrys like: Shampoo, Bar Soap, Baby Powder, Mouthwash, Toothpaste

3.Typeing paper

4.envelopes

5.Pens

6.Pencils

7.Clothes

8.CD-R Discs

9.Notebook Paper

10.ETC...

What Can I Do? I Need Help.

Questions I have:

1.Can someone help me have some money so I can have haircuts?

2.Can someone please send me some postage Stamps I am needing some Stamps?

3.Can someone please Send me a gift Card to Walmart so I can have things like

toiletrys, typeing paper, envelopes, Pens, Pencils, etc.. that I need

If you know the answers please e-mail me at :

CHANNING28105@ LYCOS.COM

CHANNING28270@ GMAIL.COM

CHANCHAN79@KITTYMAI L.COM

Channing

[Guest guest]

Speaking of Hoaxs

>

> I am a female with Autism- The Aspergers kind. I live in a group home in

Charlotte, North Carolina. I am not getting any money at all to get haircuts at

all .I cut my own hair recently because I do not get any money for haircuts and

the group home staff yelled at me . I want to get my hair straightened out and

the group home will not let me get a Haircut At All.The Group home is neglecting

the fact I still need haircuts. My Parents also yelled at me because I cut my

hair and is neglecting the fact I still need haircuts. What Can I do? My Job

which is an on Call only Job is not calling me in up to where I am not getting a

Paycheck at all. Any money that I get from the Social Security Administration

and Special Assistance all goes to pay for my Rent up to where I do not get any

money for haircuts. Other Than not getting any money for haircuts I am not

getting any money to get things like:

> 1.Postage Stamps

> 2.toiletrys like: Shampoo, Bar Soap, Baby Powder, Mouthwash, Toothpaste

> 3.Typeing paper

> 4.envelopes

> 5.Pens

> 6.Pencils

> 7.Clothes

> 8.CD-R Discs

> 9.Notebook Paper

> 10.ETC...

> What Can I Do? I Need Help.

> Questions I have:

> 1.Can someone help me have some money so I can have haircuts?

> 2.Can someone please send me some postage Stamps I am needing some Stamps?

> 3.Can someone please Send me a gift Card to Walmart so I can have things like

toiletrys, typeing paper, envelopes, Pens, Pencils, etc.. that I need

>

>

> If you know the answers please e-mail me at :

>

> CHANNING28105@...

> CHANNING28270@...

> CHANCHAN79@...

>

> Channing

>

[Guest guest]

It looks like one can try these applications from here --though I did not try

them, I'm not the happy owner of an iPhone a/o iTouch Hope it helps:

iPrompts:

http://appulo.us/appdb/?page=viewapp & id=8899

StepStones:

http://appulo.us/appdb/?page=viewapp & id=8603

Picture Scheduler:

http://appulo.us/appdb/?page=viewapp & id=8562

Text2Speech:

http://appulo.us/appdb/?page=viewapp & id=9122

ABC Sign:

http://appulo.us/appdb/?page=viewapp & id=3237

Regards from Argentina! (sorry for my English),

María Cecilia

[ ] Hello everyone

My name is Laurie and I have a 9yr old downsyndrome/autism child named Mic

and have not posted here in eons,Mic is non-verbal and is severely apraxic, I am

wondering I have seen reports that the Itouch is using applications for

communication devices, Im very interested, Mic does have a dynavox its old

outdated and heavy and Im just wondering if anyone here might have some info on

these. My understanding is the application is from itunes I am clueless after

that.And what is the app called? Thanks all, Laurie Drago

[Guest guest]

thank you Laurie

From: Madeline_wolfe@...

Date: Wed, 7 Oct 2009 13:18:13 -0300

Subject: Re: [ ] Hello everyone

It looks like one can try these applications from here --though I did not try

them, I'm not the happy owner of an iPhone a/o iTouch Hope it helps:

iPrompts:

http://appulo.us/appdb/?page=viewapp & id=8899

StepStones:

http://appulo.us/appdb/?page=viewapp & id=8603

Picture Scheduler:

http://appulo.us/appdb/?page=viewapp & id=8562

Text2Speech:

http://appulo.us/appdb/?page=viewapp & id=9122

ABC Sign:

http://appulo.us/appdb/?page=viewapp & id=3237

Regards from Argentina! (sorry for my English),

María Cecilia

[ ] Hello everyone

My name is Laurie and I have a 9yr old downsyndrome/autism child named Mic and

have not posted here in eons,Mic is non-verbal and is severely apraxic, I am

wondering I have seen reports that the Itouch is using applications for

communication devices, Im very interested, Mic does have a dynavox its old

outdated and heavy and Im just wondering if anyone here might have some info on

these. My understanding is the application is from itunes I am clueless after

that.And what is the app called? Thanks all, Laurie Drago

[Guest guest]

hi,  the ipod touch has an app called proloquo2go, i think it has 6 or 7,000

words on it

________________________________

From: h <mick8_7@...>

Sent: Wed, October 7, 2009 9:54:19 AM

Subject: [ ] Hello everyone

 

My name is Laurie and I have a 9yr old downsyndrome/ autism child named Mic and

have not posted here in eons,Mic is non-verbal and is severely apraxic, I am

wondering I have seen reports that the Itouch is using applications for

communication devices, Im very interested, Mic does have a dynavox its old

outdated and heavy and Im just wondering if anyone here might have some info on

these. My understanding is the application is from itunes I am clueless after

that.And what is the app called? Thanks all, Laurie Drago

__________________________________________________________________

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