Jacky a teenager with apraxia in Hong Kong

[Guest guest]

Hi everyone!

Until we get the new website up and going you can always find up to date info

both at Facebook http://www.apraxia.org and our Twitter updates

http://twitter.com/TheLateTalker

The following story is the amazing journey of one family from Hong Kong's on

growing up with apraxia. You'll find that even though there is a language

barrier Lily's story is pretty similar to any of ours here in the US.

Misdiagnosis -frustration over lack of services- dreams and worries for the

future.

Jacky is now a teen and it is my hope that through the new website's page we all

can help raise further awareness...perhaps help to get a support group there so

that Lily and Jacky can find other families they can hang out with, share with!

There is a huge amount of wonderful and beautiful pictures as well- some are

already uploaded to the photo section of the apraxia.org page and others will be

going up soon. Again once the new website is complete it can all be on the same

page!

Here is the link!

http://www.facebook.com/group.php?gid=115029735601#/topic.php?uid=115029735601 & t\

\

opic=9149

or as in Twitter land

http://bit.ly/L764e

Oh and one thing I found funny is that once again fish were to the rescue to

help bring better communication -Babelfish!

And this page doesn't allow me to post in Chinese like FB does- but " Talk to you

soon- and thank you Lily for sharing! " :-)

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