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We have a 20 month old toddler adopted from Georgia who has been

diagosed with verbal apraxia.His receptive speech seems fine.

His gross and fien motor skills are excellent. My question is it

possible to have verbal apraxia and still have excellent gross and

fine motor skills?

THanks! Jacky in Vancouver

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Guest guest

I know how you feel!!!! I had never heard of apraxia before my son's

diagnosis. My oldest didn't really speak until he was almost three,

although when he did speak he annunciated very clearly and I knew he

could. When he decided to talk it was in full sentences. I kept

telling myself that my youngest was going to be the same way, there

is nothing wrong, and yet my gut instinct said there was. He was so

frustrated and angry all the time, constantly screaming and whining.

We took him to our ped. and were told to get a speech evaluation. He

had severe apraxia and expressive language disorder. I was in denial

for a few days, I cried, and then I thought, I need to pull myself

together and get him the help he needs rather than sitting here like

this. So we started speech therepy and he has improved by leaps and

bounds!! He has turned into a huggy, loving little boy who likes to

be held (never before, he was always too angry), he tells me he loves

me, he sings, it's just amazing. He has been going to speech therepy

2X per week since October and I'm so glad we chose to do so instead

of ignoring it and thinking it would get better on it's own.

I'm still learning quite a bit about this condition, and so many

people have been dealing with all sorts of things relating to this

that I am soaking up everything I can on this board. I have only

been here for maybe a week and a half and the things I have learned

in that time from everyone here is priceless.

I'm sure you can find the help and support here that you are looking

for. It's so nice to talk to others who are dealing with this same

issue.

Take care

Bisel

> Hi,

> My 2 year old daughter has been diagnosed with apraxia. She has

> been seen by a developmental peditrician and is going through

speech

> therapy (for a little over a month now). She has an appointment in

2

> weeks w/ OT for poss sensory issues. I am still confused about all

> of this it is a lot to process. I have so many questions. My

husband

> is in denial. My 4 year old wants to know why I love her sister

more

> (because she takes so much more time). We are learning simple sign

> language and working on communication boards. If there is anything

I

> am missing please give me some advice. I am open to anything. I

have

> gone to some websites but there isn't too much on childhood apraxia.

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Hi Sheri,

I know how you feel, we probably all do. I was in the same situation

about 4 months ago, seems like 4 years though.

Firstly, take a big deep breath & don't panic. You are doing well by

getting her the help early & by being on this list, wanting to learn

all you can about her problem...she's lucky. Sign language was our

saving grace. Her SLP got her started & then she began making up her

own signs. She is far less frustrated & really gets her point across

most of the time.

I would then suggest RUNNING to the book store & getting a copy of

The Late Talker. I read that book & so much began to make sense to

me, it's written in easy to understand terminology. I use it now as a

refernce guide.

After reading the book & posting many quesions here, I began Callie

on fish oil, seems to be helping.

My daughter has sensory integration issues as well, she hates being

dirty, won't keep a pair of socks and/or shoes on for more than a few

minutes at a time, etc.. She has feeding, chewing, swallowing issues

as well, the OT will be helpful in that area too.

Good Luck

> Hi,

> My 2 year old daughter has been diagnosed with apraxia. She has

> been seen by a developmental peditrician and is going through

speech

> therapy (for a little over a month now). She has an appointment in

2

> weeks w/ OT for poss sensory issues. I am still confused about all

> of this it is a lot to process. I have so many questions. My

husband

> is in denial. My 4 year old wants to know why I love her sister

more

> (because she takes so much more time). We are learning simple sign

> language and working on communication boards. If there is anything

I

> am missing please give me some advice. I am open to anything. I

have

> gone to some websites but there isn't too much on childhood apraxia.

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Hi, Sheri -

Our oldest has no issues (except that she's 17 and thinks she knows

everything but, oh well!). But, our situation is a bit different - our daughter

is actually my step-daughter and our son was adopted so there wouldn't be any

genetic link to anything there. But, our dd was very advanced anyway (I came

into her life when she was 3 1/2, we adopted our son at birth). We knew there

was something different about Josh when he was 6 months - dr said to wait. We

approached the dr again at 9 months - he said to wait. At 12 months we said we

simply weren't waiting any longer and would he give us a referral to Easter

Seals for an eval - he did and, sure enough, came back with all the things I

wrote about before (except the dysarthria - that was just brought up about 3

months ago). We've been through all sorts of testing, MRI's, genetic testing,

etc. Everything comes back normal - ped neuro says it was a " prenatal accident "

whatever that means. Very frustrating to not have a

definitive answer as to why Josh has these issues but, in the long run, it's

not as important as having gotten him into therapy early.

Good luck and keep in touch.

Sherry

sheri_coon <madicoon@...> wrote:

Thank you so much for responding. I'm glad to know that I am not

alone. My 4 year old was speaking complete sentences at a little

over a year and you could understand everything. She could do

picture flash cards at 9 months. I kept telling my peditricain that

something was wrong with and he would say you know that you

can't compare children, let's wait till she is 2 then we will start

worring. After that I felt a little better till I saw the comercial

for Early Steps. I called the number and they said I should have

called them at 18 months. I have been very happy with the program so

far. All my daughter can say is " a my " Like I said we are working

with sign language so we can communicate. It breaks my heart when

she tells me I Love You!!! I know that it will get better. I just

wish she could talk to me. We both get so frustrated when we can't

figure out what she wants. She has gotten to where she will hit or

pinch if you don't understand her. Does your oldest have any sensory

issues? Mine doesn't like water ( we haave to take a bath

together),she doesn't chew her food she swallows whole, doesn't like

to be dirty. I had her evaluated for Autisim but that wasn't the

case. She scored poorly in the speech and change ability of the

test. The Dr. thought it was because of the Apraxia though. She will

re-eval in the spring before she starts pre-school. Thank you again

for listening to me. If I can be of any help to you please e-mail me.

Thanks,

Sheri

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Hi Sheri,

I am also new to the diagnosis of apraxia and this group. In fact

this is my first post!! It will be nice to be able to go through

this with someone else and support of this group. My son is 33

months old and has been in EI since 19 months and a private SLP

2xweek. There is so much to process it is unreal.

angie

> Hi,

> My 2 year old daughter has been diagnosed with apraxia. She

has

> been seen by a developmental peditrician and is going through

speech

> therapy (for a little over a month now). She has an appointment in

2

> weeks w/ OT for poss sensory issues. I am still confused about all

> of this it is a lot to process. I have so many questions. My

husband

> is in denial. My 4 year old wants to know why I love her sister

more

> (because she takes so much more time). We are learning simple sign

> language and working on communication boards. If there is anything

I

> am missing please give me some advice. I am open to anything. I

have

> gone to some websites but there isn't too much on childhood

apraxia.

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