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RE: Symposium on Apraxia

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I just read em on Apraxia kids about a symposium taht is scheduled for 2/28-

3/2/02

Where is it being held? How is registration is being handled? Is there a web

site/Tel no?

Tatyana

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Hi Tatyana,

The information is at http://www.apraxia.org/indexoverview.html It's

wonderful that so many are getting together: it would have been even

better if they included some pediatric neuroscientists and

neurodevelopmental doctors as well. The Apraxia Kids conference is

not open to parents either. When CHERAB hosted the First Apraxia

Conference speech professionals on the board for Apraxia Kids were

invited and declined attending.

All of us from CHERAB believe it best for everyone to put aside

personal opinion and come together with open minds. Going ahead I'm

sure that will be done. I have already spoken to a few of the speech

PhD presenters at the Apraxia Kids conference about that, as well as

a University Hospital we may be working with. Anything that CHERAB

hosts will be open to all professionals, organizations, and

parents out there that can help our children. I know the University

Hospital I just met with strongly respects the input of the parents,

the neuromedical research doctors take the input from the parents

seriously. As Sallie Bernard told me, bringing researchers together

with parents is the new trend in research. When it comes to our

children, time is precious and the sooner all opinions and ideas come

together from all sides, medical, speech, educational, and parents,

the sooner we may reach conclusions that may really help, vs. more

separation. If doctors have one belief and speech professionals have

another where does that leave our children?

Well I guess everything starts somewhere. My belief is that when you

come to a wall you look for a door. If there is none - why bother

knocking down the wall when you can just as easily go over it or

around it?!

=====

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