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~Emily's Apraxia~

This blog is about my daughter Emily. She was diagnosed with a neurological speech disorder called Apraxia just before her 3rd birthday. My hopes for this blog are to educate people about this unknown disorder called Apraxia, to show that apraxia has no face & to reach out to other families going through the same things as we are.

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~Emily's Apraxia~ | emilysapraxia.blogspot.com Reviews
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This blog is about my daughter Emily. She was diagnosed with a neurological speech disorder called Apraxia just before her 3rd birthday. My hopes for this blog are to educate people about this unknown disorder called Apraxia, to show that apraxia has no face &amp;amp; to reach out to other families going through the same things as we are.
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1 emily's apraxia
2 silly little update
3 she loves dance
4 crazy
5 posted by
6 alicia
7 1 comment
8 catching up
9 no comments
10 older posts
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emily's apraxia,silly little update,she loves dance,crazy,posted by,alicia,1 comment,catching up,no comments,older posts,about me,united states,emily's helpful links,apraxia kids,the late talker,apraxia speaks,signing time,asl pro,super duper publications
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~Emily's Apraxia~ | emilysapraxia.blogspot.com Reviews

https://emilysapraxia.blogspot.com

This blog is about my daughter Emily. She was diagnosed with a neurological speech disorder called Apraxia just before her 3rd birthday. My hopes for this blog are to educate people about this unknown disorder called Apraxia, to show that apraxia has no face &amp;amp; to reach out to other families going through the same things as we are.

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emilysapraxia.blogspot.com emilysapraxia.blogspot.com
1

~Emily's Apraxia~: The craziness of January!

http://emilysapraxia.blogspot.com/2010/01/craziness-of-january.html

This blog is about my daughter Emily. She was diagnosed with a neurological speech disorder called Apraxia just before her 3rd birthday. My hopes for this blog are to educate people about this unknown disorder called Apraxia, to show that apraxia has no face and to reach out to other families going through the same things as we are. Friday, January 29, 2010. The craziness of January! So we are now forced to either pay out-of-network costs, privately or find a whole new provider! On a totally different no...

2

~Emily's Apraxia~: July 2009

http://emilysapraxia.blogspot.com/2009_07_01_archive.html

This blog is about my daughter Emily. She was diagnosed with a neurological speech disorder called Apraxia just before her 3rd birthday. My hopes for this blog are to educate people about this unknown disorder called Apraxia, to show that apraxia has no face and to reach out to other families going through the same things as we are. Sunday, July 12, 2009. New Article on Apraxia Reaserch. SYNDROME OF ALLERGY, APRAXIA, AND MALABSORPTION: CHARACTERIZATION OF A NEURODEVELOPMENTAL PHENOTYPE. It really just va...

3

~Emily's Apraxia~: April 2009

http://emilysapraxia.blogspot.com/2009_04_01_archive.html

This blog is about my daughter Emily. She was diagnosed with a neurological speech disorder called Apraxia just before her 3rd birthday. My hopes for this blog are to educate people about this unknown disorder called Apraxia, to show that apraxia has no face and to reach out to other families going through the same things as we are. Wednesday, April 22, 2009. Links to this post. Monday, April 20, 2009. Birthday, Easter and Buckets. For her Birthday she picked Minnie Mouse! She loves Minnie Mouse! I tried...

4

~Emily's Apraxia~

http://emilysapraxia.blogspot.com/2010/01/wow-august-has-it-really-been-that-long.html

This blog is about my daughter Emily. She was diagnosed with a neurological speech disorder called Apraxia just before her 3rd birthday. My hopes for this blog are to educate people about this unknown disorder called Apraxia, to show that apraxia has no face and to reach out to other families going through the same things as we are. Sunday, January 10, 2010. August, has it really been that long since I have updated here! Emily is doing fantastic! I am now considering getting her a speech program develope...

5

~Emily's Apraxia~

http://emilysapraxia.blogspot.com/2009/02/funding-cuts-state-of-arizona-has-cut.html

This blog is about my daughter Emily. She was diagnosed with a neurological speech disorder called Apraxia just before her 3rd birthday. My hopes for this blog are to educate people about this unknown disorder called Apraxia, to show that apraxia has no face and to reach out to other families going through the same things as we are. Saturday, February 28, 2009. The State of Arizona has cut AzEIP funding. Emily will now only receive 1 hour of speech therapy a month! February 26, 2009. Our management team ...

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~Emily's Apraxia~

This blog is about my daughter Emily. She was diagnosed with a neurological speech disorder called Apraxia just before her 3rd birthday. My hopes for this blog are to educate people about this unknown disorder called Apraxia, to show that apraxia has no face and to reach out to other families going through the same things as we are. Wednesday, February 24, 2010. Here I am looking at Emily's page trying to figure out what's missing.well could it be new pictures? Emily is doing fantasitc! Links to this post.

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