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BFL Women - remember to vote for 's Blog - it jumped WAY ahead when we

all first found out about it so let's keep voting so she'll win! Vote Skwigg

Blog!

http://www.blogmechanics.com/bob/vote.php?pollID=12

<http://www.blogmechanics.com/bob/vote.php?pollID=12 & PHPSESSID=f6116c812b48e

dff5babeed0eaf70395> & PHPSESSID=f6116c812b48edff5babeed0eaf70395

_____

From: joys93gt@... [mailto:joys93gt@...]

Sent: Friday, 07 January, 2005 9:33 AM

Subject: 's blog

HAHAHAHHAAAA!! I just read 's blog- the part about VH1's making over

Vince Neil! What a riot!! I saw it too and loved your take on it : )

Sorry, this was a bit off topic, but so funny. (Oh, and I voted again while

I was there)

Joy

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My husband was telling me about that VH1 show last night. It just so

happens that Motley Crue will be touring and will be in Moline, IL so

we'll be going to see them! Whohoo! I love Motley Crue, bring back

the 80s!! My husband, being a drummer, is in love w/Tommy Lee.

> HAHAHAHHAAAA!! I just read 's blog- the part about VH1's

making over Vince Neil! What a riot!! I saw it too and loved your

take on it : ) Sorry, this was a bit off topic, but so funny.

(Oh, and I voted again while I was there)

>

> Joy

>

>

>

>

>

>

>

>

>

>

>

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I, too, love the Crue...the problem is it is the same with Van Halen....they

just aren't the same without all the original guys making music together! Lucky

you getting to see them in concert!

Yeah, and I love Tommy too, but it aint cuz he's a drummer-----whoooo naughty :

)

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I am also in love with Tommy Lee...but for completely different

reasons. Rowr!

> > HAHAHAHHAAAA!! I just read 's blog- the part about VH1's

> making over Vince Neil! What a riot!! I saw it too and loved

your

> take on it : ) Sorry, this was a bit off topic, but so funny.

> (Oh, and I voted again while I was there)

> >

> > Joy

> >

> >

> >

> >

> >

> >

> >

> >

> >

> >

> >

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I am also in love with Tommy Lee...but for completely different

reasons. Rowr!

> > HAHAHAHHAAAA!! I just read 's blog- the part about VH1's

> making over Vince Neil! What a riot!! I saw it too and loved

your

> take on it : ) Sorry, this was a bit off topic, but so funny.

> (Oh, and I voted again while I was there)

> >

> > Joy

> >

> >

> >

> >

> >

> >

> >

> >

> >

> >

> >

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Well, I am shocked and appalled! No I'm not!!!! LOL at you and

Ruth, you 2 naughty girls!!!

> I, too, love the Crue...the problem is it is the same with Van

Halen....they just aren't the same without all the original guys

making music together! Lucky you getting to see them in concert!

>

> Yeah, and I love Tommy too, but it aint cuz he's a drummer-----

whoooo naughty : )

>

>

>

>

>

>

>

>

>

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  • 8 months later...

Seeeeee!! I'm not crazy. Well.... mostly not crazy. LOL

On 9/29/05, Pamela <angelwolf00@...> wrote:

> I was reading your blog yesterday and thought how strange about the

> Sudafed. Well, I go to get my tires serviced this morning, and decide to

> stop by Walgreen's to get some Benadryl Head and Sinus. I find out I have

> to take a little card to the register where they go and pull the

> medication, they no longer keep it on the shelf. I had to show my license

> and sign for the stuff. The pharmacy tech said it is a new law. Certain

> medications with certain ingredients are not allowed on the shelf anymore.

> They did have the Benadryl Allergy medication still on the shelf, this

> medication doesn't the same ingredients.

>

> Pam

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Skwigg wrote:

> Seeeeee!! I'm not crazy. Well.... mostly not crazy. LOL

>

>

Here in georgia it's the same way. They've done some major busts here.

--

|Demoness Abigor|net.goth|The Pinkest Deceptagon in da world!

|AIM|AbigorBot|

|Josh: you mentioned Transformers! and didn't use the words " are lame " in the

same sentence! you

are my dream girl!

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I think it's the pseudoephedrine... the druggies use it to make

crystal meth.

Deb

> > Seeeeee!! I'm not crazy. Well.... mostly not crazy. LOL

> >

> >

>

> Here in georgia it's the same way. They've done some major busts

here.

> --

> |Demoness Abigor|net.goth|The Pinkest Deceptagon in da world!

> |AIM|AbigorBot|

> |Josh: you mentioned Transformers! and didn't use the words " are

lame " in the same sentence! you

> are my dream girl!

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> I think it's the pseudoephedrine... the druggies use it to make

> crystal meth.

Its one of those stupid laws that just basically infringes on your

rights to over the counter medications. Drug addicts by wholesale from

peope who deal in LARGE quantities bought underground from

pharmaceutical companies etc, NOT emptying thousands of teeny capsules

they buy from drugstores .. Good thing its not rampant yet here in

California where people can still buy cold meds without showing their

drivers license.. geesh ..

joni

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

*It's often said that life is strange. But compared to what?*

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> .. Good thing its not rampant yet here in

> California where people can still buy cold meds without showing their

> drivers license.. geesh ..

>

But I notice that Walmart does limit how much allergy/cold meds I can

get at one time. :(

Colleen

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So does Costco - one time I was trying to get three different medicines,

cough syrup, daytime cold stuff and nighttime stuff. I think the limit is

three per purchase and my problem was that the syrup came in a pack of 2. Of

course I didn't realize that they count each bottle because it was packaged

as one item. I was really grumpy then, fighting a bad cold. :)

Leah S

> But I notice that Walmart does limit how much allergy/cold meds I can

> get at one time. :(

>

> Colleen

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  • 1 year later...
Guest guest

My son Garrett who is 8 now would have fit your discription of your son

perfectly at that age. Garrett could not communicate his needs and we

found it very frustrating to know what he wanted. We turned to a program

called early intervention for support and took Garrett to play groups

that included structured activities with other children with special

needs. There he received group as well as one on one intervention that

helped him learn that in order to have fun with other children he had to

use his words. We had to use a kind of tough love stradegy that involved

not giving him what he wanted unless he used the sign language or words

to ask for it. When you are sitting around the table with six other kids

and everyone else gets juice and snack eventually the child will

communicate his needs and say juice or sign it. From there we move onto

phrases like I want Juice Please. I was worried that Garrett would be

resentful or upset with us because we forced him to communicate, but in

the end we have a little boy who is fully capable of telling me anything

that he chooses and getting his needs across. I am not usre if this

method would work with your son, but I didn't even kno my son had Autism

and I guess I treated him like a capable child and he met the

challanges. I wish you luck because it was not as simple as it seems

now.... We went through many years of speech therapy and many years of

miscomunication to get where we are today. I hope your son does as well.

By the way, my son still does not make good eye contact. It is something

that we still practice. Also do not mistake his lack of interest in what

you are saying for not understanding. I did that for a long time, but

found out that if I repeat myself several times he always has the right

answer. I just have to find it. My son still have problem dressing

himself and just recently learned how to do buttons and snaps well. Most

mornings I still have to help him put on his shoes and it requires

constant prompting for him to get ready to go anywhere. Repetiotion

seems to be key with my son. I can never tell him something enough

times.

Janie

>

> Our little boy was formally diagnosed with Autism last Friday.

> He is 2 years and 2 months old and an amazing little boy. He says a

> few single words, but inconsistently and although he used to point, he

> very rarely points anymore. We're hoping to begin the GFCF diet and

> try some anti fungal treatment with the help of a Consultant later in

> the year. At the moment he has no tools to ask for what he wants (even

> though he says around 30 words), other than screaming and looking at

> the object. Does anyone have a tip on how to get him to give us eye

> contact when he wants something, or how to encourage him to point at

> what he wants? He has an hours therapy each week for communication and

> social development but his speech and communication really aren't

> showing signs of improvement at the moment. His general development is

> a little behind (he cannot dress, undress or feed himself very well),

> though he's just started naming some shapes and can identify the

> letters o and e. He is obsessed with signs, road signs, shop signs etc

> and is extremely musical. He can repeat a tune after hearing it just

> once, and has perfect pitch. The experts say they feel he will be high

> functioning (as he smiles at them and appears social), yet they are

> unable to say whether or not he will ever develop functional speech.

> His understanding is very poor and he does not understand much of what

> we say and rarely follows single word comprehension tasks. For

> example, this morning I asked him " where is your teddy " and he pointed

> to his own nose, yet at other times he seems to know the word for

teddy.

>

> I have made a blog for as a way of sharing thoughts and

> recording his longterm progress so that we can refer back and see

> improvements in his progress. Here's the link

> http://homepage.ntlworld.com/pernod/blog/

>

> I wish to say thank you very much to everyone who wrote to us earlier

> in the year - we did read all the e-mails and really appreciated the

> advice. If anyone has any further advice for us (and ideas how to

> encourage to communicate and give eye contact), please e-mail

> us through 's blog.

>

> Regards,

>

>

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Guest guest

My son Garrett who is 8 now would have fit your discription of your son

perfectly at that age. Garrett could not communicate his needs and we

found it very frustrating to know what he wanted. We turned to a program

called early intervention for support and took Garrett to play groups

that included structured activities with other children with special

needs. There he received group as well as one on one intervention that

helped him learn that in order to have fun with other children he had to

use his words. We had to use a kind of tough love stradegy that involved

not giving him what he wanted unless he used the sign language or words

to ask for it. When you are sitting around the table with six other kids

and everyone else gets juice and snack eventually the child will

communicate his needs and say juice or sign it. From there we move onto

phrases like I want Juice Please. I was worried that Garrett would be

resentful or upset with us because we forced him to communicate, but in

the end we have a little boy who is fully capable of telling me anything

that he chooses and getting his needs across. I am not usre if this

method would work with your son, but I didn't even kno my son had Autism

and I guess I treated him like a capable child and he met the

challanges. I wish you luck because it was not as simple as it seems

now.... We went through many years of speech therapy and many years of

miscomunication to get where we are today. I hope your son does as well.

By the way, my son still does not make good eye contact. It is something

that we still practice. Also do not mistake his lack of interest in what

you are saying for not understanding. I did that for a long time, but

found out that if I repeat myself several times he always has the right

answer. I just have to find it. My son still have problem dressing

himself and just recently learned how to do buttons and snaps well. Most

mornings I still have to help him put on his shoes and it requires

constant prompting for him to get ready to go anywhere. Repetiotion

seems to be key with my son. I can never tell him something enough

times.

Janie

>

> Our little boy was formally diagnosed with Autism last Friday.

> He is 2 years and 2 months old and an amazing little boy. He says a

> few single words, but inconsistently and although he used to point, he

> very rarely points anymore. We're hoping to begin the GFCF diet and

> try some anti fungal treatment with the help of a Consultant later in

> the year. At the moment he has no tools to ask for what he wants (even

> though he says around 30 words), other than screaming and looking at

> the object. Does anyone have a tip on how to get him to give us eye

> contact when he wants something, or how to encourage him to point at

> what he wants? He has an hours therapy each week for communication and

> social development but his speech and communication really aren't

> showing signs of improvement at the moment. His general development is

> a little behind (he cannot dress, undress or feed himself very well),

> though he's just started naming some shapes and can identify the

> letters o and e. He is obsessed with signs, road signs, shop signs etc

> and is extremely musical. He can repeat a tune after hearing it just

> once, and has perfect pitch. The experts say they feel he will be high

> functioning (as he smiles at them and appears social), yet they are

> unable to say whether or not he will ever develop functional speech.

> His understanding is very poor and he does not understand much of what

> we say and rarely follows single word comprehension tasks. For

> example, this morning I asked him " where is your teddy " and he pointed

> to his own nose, yet at other times he seems to know the word for

teddy.

>

> I have made a blog for as a way of sharing thoughts and

> recording his longterm progress so that we can refer back and see

> improvements in his progress. Here's the link

> http://homepage.ntlworld.com/pernod/blog/

>

> I wish to say thank you very much to everyone who wrote to us earlier

> in the year - we did read all the e-mails and really appreciated the

> advice. If anyone has any further advice for us (and ideas how to

> encourage to communicate and give eye contact), please e-mail

> us through 's blog.

>

> Regards,

>

>

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Guest guest

My son Dylan who is now 13 sounds exactly like your child at his age.

When he was three we put him in the pre-school handicapp program in

our school district. They work on speech, occupational, and social

skills. It was a blessing!! We also took him to our local hospital

for speech therapy once a week.

He did not sppeek till he was 4 and then only a few words. It wasn;t

until around 5 that his speech " exploded " He had articulation

problems but could say so much and just continued to add words to

his repitore.

When he wanted something we held his face to us and said dylan look

at us when you are talking to us.

After years of this he no longer has problems with eye contact and

realizes now how important it is.

Just keep working with him and If he is like my son he will come

around when he is ready.

In , " janiemop30 " <jsilance@...>

wrote:

>

>

> My son Garrett who is 8 now would have fit your discription of

your son

> perfectly at that age. Garrett could not communicate his needs and

we

> found it very frustrating to know what he wanted. We turned to a

program

> called early intervention for support and took Garrett to play

groups

> that included structured activities with other children with

special

> needs. There he received group as well as one on one intervention

that

> helped him learn that in order to have fun with other children he

had to

> use his words. We had to use a kind of tough love stradegy that

involved

> not giving him what he wanted unless he used the sign language or

words

> to ask for it. When you are sitting around the table with six

other kids

> and everyone else gets juice and snack eventually the child will

> communicate his needs and say juice or sign it. From there we move

onto

> phrases like I want Juice Please. I was worried that Garrett would

be

> resentful or upset with us because we forced him to communicate,

but in

> the end we have a little boy who is fully capable of telling me

anything

> that he chooses and getting his needs across. I am not usre if this

> method would work with your son, but I didn't even kno my son had

Autism

> and I guess I treated him like a capable child and he met the

> challanges. I wish you luck because it was not as simple as it

seems

> now.... We went through many years of speech therapy and many

years of

> miscomunication to get where we are today. I hope your son does as

well.

> By the way, my son still does not make good eye contact. It is

something

> that we still practice. Also do not mistake his lack of interest

in what

> you are saying for not understanding. I did that for a long time,

but

> found out that if I repeat myself several times he always has the

right

> answer. I just have to find it. My son still have problem dressing

> himself and just recently learned how to do buttons and snaps

well. Most

> mornings I still have to help him put on his shoes and it requires

> constant prompting for him to get ready to go anywhere. Repetiotion

> seems to be key with my son. I can never tell him something enough

> times.

>

>

>

> Janie

>

>

>

>

>

>

>

>

>

> >

> > Our little boy was formally diagnosed with Autism last

Friday.

> > He is 2 years and 2 months old and an amazing little boy. He

says a

> > few single words, but inconsistently and although he used to

point, he

> > very rarely points anymore. We're hoping to begin the GFCF diet

and

> > try some anti fungal treatment with the help of a Consultant

later in

> > the year. At the moment he has no tools to ask for what he wants

(even

> > though he says around 30 words), other than screaming and

looking at

> > the object. Does anyone have a tip on how to get him to give us

eye

> > contact when he wants something, or how to encourage him to

point at

> > what he wants? He has an hours therapy each week for

communication and

> > social development but his speech and communication really aren't

> > showing signs of improvement at the moment. His general

development is

> > a little behind (he cannot dress, undress or feed himself very

well),

> > though he's just started naming some shapes and can identify the

> > letters o and e. He is obsessed with signs, road signs, shop

signs etc

> > and is extremely musical. He can repeat a tune after hearing it

just

> > once, and has perfect pitch. The experts say they feel he will

be high

> > functioning (as he smiles at them and appears social), yet they

are

> > unable to say whether or not he will ever develop functional

speech.

> > His understanding is very poor and he does not understand much

of what

> > we say and rarely follows single word comprehension tasks. For

> > example, this morning I asked him " where is your teddy " and he

pointed

> > to his own nose, yet at other times he seems to know the word for

> teddy.

> >

> > I have made a blog for as a way of sharing thoughts and

> > recording his longterm progress so that we can refer back and see

> > improvements in his progress. Here's the link

> > http://homepage.ntlworld.com/pernod/blog/

> >

> > I wish to say thank you very much to everyone who wrote to us

earlier

> > in the year - we did read all the e-mails and really appreciated

the

> > advice. If anyone has any further advice for us (and ideas how to

> > encourage to communicate and give eye contact), please e-

mail

> > us through 's blog.

> >

> > Regards,

> >

> >

>

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Guest guest

Hi Janie

Thank you so much for telling me about your son and for your support

and sharing your experiences. I agree very much with your point about

repetition. requires lots and lots of repetition in order to

understand what is expected. We find that there aren't many services

in the South of England for Autism - we would like to try ABA but

aren't sure where to start in our area.

Sounds like you've got a wonderful little boy there.

Regards,

cherimoya@...

> >

> > Our little boy was formally diagnosed with Autism last Friday.

> > He is 2 years and 2 months old and an amazing little boy. He says a

> > few single words, but inconsistently and although he used to point, he

> > very rarely points anymore. We're hoping to begin the GFCF diet and

> > try some anti fungal treatment with the help of a Consultant later in

> > the year. At the moment he has no tools to ask for what he wants (even

> > though he says around 30 words), other than screaming and looking at

> > the object. Does anyone have a tip on how to get him to give us eye

> > contact when he wants something, or how to encourage him to point at

> > what he wants? He has an hours therapy each week for communication and

> > social development but his speech and communication really aren't

> > showing signs of improvement at the moment. His general development is

> > a little behind (he cannot dress, undress or feed himself very well),

> > though he's just started naming some shapes and can identify the

> > letters o and e. He is obsessed with signs, road signs, shop signs etc

> > and is extremely musical. He can repeat a tune after hearing it just

> > once, and has perfect pitch. The experts say they feel he will be high

> > functioning (as he smiles at them and appears social), yet they are

> > unable to say whether or not he will ever develop functional speech.

> > His understanding is very poor and he does not understand much of what

> > we say and rarely follows single word comprehension tasks. For

> > example, this morning I asked him " where is your teddy " and he pointed

> > to his own nose, yet at other times he seems to know the word for

> teddy.

> >

> > I have made a blog for as a way of sharing thoughts and

> > recording his longterm progress so that we can refer back and see

> > improvements in his progress. Here's the link

> > http://homepage.ntlworld.com/pernod/blog/

> >

> > I wish to say thank you very much to everyone who wrote to us earlier

> > in the year - we did read all the e-mails and really appreciated the

> > advice. If anyone has any further advice for us (and ideas how to

> > encourage to communicate and give eye contact), please e-mail

> > us through 's blog.

> >

> > Regards,

> >

> >

>

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Guest guest

i have found that if you take a child's hands and place them on either side of your face they will reflexively make eye contact. make sure you praise him for "good looking."

as for pointing to what he wants, take his hand and prompt him (physically make him) point to the object. this should eventually lead to him doing this independently. good luck!!

I LOVE SOMEONE WITH AUTISM AOL now offers free email to everyone. Find out more about what's free from AOL at AOL.com.

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Guest guest

Hi ,

Don't worry about eye-contact. Many people with ASD will tell you that it is

physically painful for them to do this, and for all, or nearly all, they

find that making eye contact just distracts them so they cannot attend to

anything else, like what a person is saying. Your little boy is very young -

you may find it will improve as he grows - best not to force it.

For communication, try PECS. You need a set of laminated pictures which he

gives you to ask for something (and which you use reciprocally).

in England

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Guest guest

I agree. It took my son a long time to look into people eyes when communicating. Now he si 9 and does it most of the time. You still have to remind him once in a while but he doesn't get frustrated. Rowell <nancy@...> wrote: Hi ,Don't worry about eye-contact. Many people with ASD will tell you that it is physically painful for them to do this, and for all, or nearly all, they find that making eye contact just distracts them so they cannot attend to anything else, like what a person

is saying. Your little boy is very young - you may find it will improve as he grows - best not to force it.For communication, try PECS. You need a set of laminated pictures which he gives you to ask for something (and which you use reciprocally). in EnglandAlly

TV dinner still cooling?Check out "Tonight's Picks" on TV.

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Guest guest

My daughter has the same diagnosis at that age. She did the exact same things your son does. I started uses sign language with her. I brought some signing videos (einstein and my baby can talk). She is now 3 and is saying some words. She is also knows names of people. Most which were from the videos. She also communicates with me with simple signing.If she is hungry she will sign the word eat. If she is done then she signs the word all done. When she is signing she says the word. The only thing she still can't do is answer questions. <yvonne_uk_ok@...> wrote: Our little boy was formally diagnosed with Autism last Friday.He is 2 years and 2 months old and an amazing little boy. He says afew single words, but inconsistently and although he used to point, hevery rarely points anymore. We're hoping to begin the GFCF diet andtry some anti fungal treatment with the help of a Consultant later inthe year. At the moment he has no tools to ask for what he wants (eventhough he says around 30 words), other than screaming and looking atthe object. Does anyone have a tip on how to get him to give us eyecontact when he wants something, or how to encourage him to point atwhat he wants? He has an hours therapy each week for communication andsocial development but his speech and communication really aren'tshowing signs of improvement at the moment. His general development isa little behind (he cannot dress,

undress or feed himself very well),though he's just started naming some shapes and can identify the letters o and e. He is obsessed with signs, road signs, shop signs etcand is extremely musical. He can repeat a tune after hearing it justonce, and has perfect pitch. The experts say they feel he will be highfunctioning (as he smiles at them and appears social), yet they areunable to say whether or not he will ever develop functional speech.His understanding is very poor and he does not understand much of whatwe say and rarely follows single word comprehension tasks. Forexample, this morning I asked him "where is your teddy" and he pointedto his own nose, yet at other times he seems to know the word for teddy.I have made a blog for as a way of sharing thoughts andrecording his longterm progress so that we can refer back and seeimprovements in his progress. Here's the link http://homepage.ntlworld.com/pernod/blog/I wish to say thank you very much to everyone who wrote to us earlierin the year - we did read all the e-mails and really appreciated theadvice. If anyone has any further advice for us (and ideas how toencourage to communicate and give eye contact), please e-mailus through 's blog.Regards,Ally

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Guest guest

Thank you. It is lovely to hear from someone else in England.

Regards,

cherimoya@...

>

> Hi ,

> Don't worry about eye-contact. Many people with ASD will tell you

that it is

> physically painful for them to do this, and for all, or nearly all,

they

> find that making eye contact just distracts them so they cannot

attend to

> anything else, like what a person is saying. Your little boy is very

young -

> you may find it will improve as he grows - best not to force it.

>

> For communication, try PECS. You need a set of laminated pictures

which he

> gives you to ask for something (and which you use reciprocally).

>

> in England

>

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Another great video is "Treasure Chest" it has signs but also try "Baby Babble" which was made by speech therapistsAlly Fortney <afortney74@...> wrote: My daughter has the same diagnosis at that age. She did the exact same things your son does. I started uses sign language with her. I brought some signing videos (einstein and my baby can talk). She is now 3 and is saying some words. She is also knows names of people. Most which were from the videos. She also communicates with me with

simple signing.If she is hungry she will sign the word eat. If she is done then she signs the word all done. When she is signing she says the word. The only thing she still can't do is answer questions. <yvonne_uk_ok (DOT) co.uk> wrote: Our little boy was formally diagnosed with Autism last Friday.He is 2 years and 2 months old and an amazing little boy. He says afew single words, but inconsistently and although he used to point, hevery rarely points anymore. We're hoping to begin the GFCF diet andtry some anti fungal treatment with the help of a Consultant later inthe year. At the moment he has no tools to ask for what he wants (eventhough he says around 30 words), other than screaming and looking atthe object. Does anyone have a tip on how to get him to give us

eyecontact when he wants something, or how to encourage him to point atwhat he wants? He has an hours therapy each week for communication andsocial development but his speech and communication really aren'tshowing signs of improvement at the moment. His general development isa little behind (he cannot dress, undress or feed himself very well),though he's just started naming some shapes and can identify the letters o and e. He is obsessed with signs, road signs, shop signs etcand is extremely musical. He can repeat a tune after hearing it justonce, and has perfect pitch. The experts say they feel he will be highfunctioning (as he smiles at them and appears social), yet they areunable to say whether or not he will ever develop functional speech.His understanding is very poor and he does not understand much of whatwe say and rarely follows single word comprehension tasks. Forexample, this morning I asked him "where is

your teddy" and he pointedto his own nose, yet at other times he seems to know the word for teddy.I have made a blog for as a way of sharing thoughts andrecording his longterm progress so that we can refer back and seeimprovements in his progress. Here's the link http://homepage.ntlworld.com/pernod/blog/I wish to say thank you very much to everyone who wrote to us earlierin the year - we did read all the e-mails and really appreciated theadvice. If anyone has any further advice for us (and ideas how toencourage to communicate and give eye contact), please e-mailus through 's blog.Regards, Ally Never miss an email again! Toolbar alerts you the instant new Mail arrives. Check it out.

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People often have good luck using either sign language or PECS (picture

exchange). Sign language might be difficult if he has motor issues but if not,

get a basic book and teach him signs for things he will use/need. If signing

isn't doable, pecs are a good alternative. You can make your own even. Just

make tiny icons for common things he uses or needs. So when he wants something,

he can hand you the pecs and you know what he wants. Then be sure and reinforce

the word and try to get him to say it before giving him what he wants.

Roxanna

( ) 's Blog

Our little boy was formally diagnosed with Autism last Friday.

He is 2 years and 2 months old and an amazing little boy. He says a

few single words, but inconsistently and although he used to point, he

very rarely points anymore. We're hoping to begin the GFCF diet and

try some anti fungal treatment with the help of a Consultant later in

the year. At the moment he has no tools to ask for what he wants (even

though he says around 30 words), other than screaming and looking at

the object. Does anyone have a tip on how to get him to give us eye

contact when he wants something, or how to encourage him to point at

what he wants? He has an hours therapy each week for communication and

social development but his speech and communication really aren't

showing signs of improvement at the moment. His general development is

a little behind (he cannot dress, undress or feed himself very well),

though he's just started naming some shapes and can identify the

letters o and e. He is obsessed with signs, road signs, shop signs etc

and is extremely musical. He can repeat a tune after hearing it just

once, and has perfect pitch. The experts say they feel he will be high

functioning (as he smiles at them and appears social), yet they are

unable to say whether or not he will ever develop functional speech.

His understanding is very poor and he does not understand much of what

we say and rarely follows single word comprehension tasks. For

example, this morning I asked him " where is your teddy " and he pointed

to his own nose, yet at other times he seems to know the word for teddy.

I have made a blog for as a way of sharing thoughts and

recording his longterm progress so that we can refer back and see

improvements in his progress. Here's the link

http://homepage.ntlworld.com/pernod/blog/

I wish to say thank you very much to everyone who wrote to us earlier

in the year - we did read all the e-mails and really appreciated the

advice. If anyone has any further advice for us (and ideas how to

encourage to communicate and give eye contact), please e-mail

us through 's blog.

Regards,

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  • 1 year later...

hi sandy - i clicked on the link but couldn't get to your blog. i would love

to see it.

christy

tommy & michael's mom

**************AOL Search: Your one stop for directions, recipes and all other

Holiday needs. Search Now.

(http://pr.atwola.com/promoclk/100000075x1212792382x1200798498/aol?redir=http://\

searchblog.aol.com/2008/11/04/happy-holidays-from

-aol-search/?ncid=emlcntussear00000001)

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Hi there. My name is Tara and I have a 2 year old little girl named . I

read your blog and felt like I was reading about my daughter except for the

seizures. She also had normal scores after a scheduled c-sec but when she came

out they said she wasn't breathing. How she had a normal score is beyond me but

she did start breathing right away. I often blame myself for her health issues .

I felt like it was too early to have her but I let my doctors office talk me

into it. (my first child was 10lbs 2 oz) She was born at 37 weeks and weighed

only 6 pounds. She stayed in the Nicu for 4 days because of apnea. She ended up

coming home on an apnea monitor for over a year , screamed almost everyday until

at 5 months when she went in the hospital for double hernia surgery and the

doctors there realized she had silent reflux, (put on prevacid) . also

has a very deep dimple at the end of her tailbone that they originally thought

was an open but as they looked into it they were wrong. She then started p/t

because of torticollis and when that was resolved they realized she had

hypotonia. We were told she may never walk (started walking right before her 2nd

birthday) At about a year and a half we started s/t but I was not too worried or

aggressive enough as I thought she wasn't talking because she was working so

hard on her walking. Little did I know she would be diagnosed @ 2years with

apraxia. It has been a very hard struggle for . I can remember when she

was on the apnea monitor and it would go off in the middle of the night ( I did

not sleep at all the first year) many nights in the hospital, and I would say

God in a year this will all be a memory, If I can just get through this year.

Then the screaming started, (before I knew it was relux they said she was colic)

and I would cry with her and think in a year this will all be a memory, then the

prevacid kicked in. Then we realized her head was flat and we started the p/t (4

xs a week) all this while working a full time job and trying to be a good mom

to my 3 year old . I just kept thinking in a year this will be a memory and

instead of therapy I'll have mommy and me and the pitter patter of 2 children

running around my house , playing, giggling best friends.Then wouldn't

crawl, (welcome to hypotonia) my therapists said give her a year, she will

crawl. Then welcome to Apraxia. I guess you can see where this is going. I 'm

finally beginning to come to terms that it is what it is. I try not to put a

timetable on anything anymore. I would never trade for anything in the

world, despite all her struggles she is the sweetest, most affectionate, smart,

funny child. Still I find myself angry at the world and sad for s future

struggles. I hope one day this all will be a memory but if not I am learning to

cope one day at a time. So sorry for the rambling but I'm having one of those

(why days) I almost just deleted this email but I thought you should

know I feel better that I read your blog and just wanted you to know that. It

feels good to know your not alone.

-------------- Original message from " sandy_tanana " <sandy_tanana@...>:

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

Check out 's blog- I finally got it started.

Sandy

http://www.nataliehopesjourney1.blogspot.com/

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