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God's Gift From Heaven
 
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Welcome to MY ANGEL DANIELLE!  Thank you for your interest in our baby girl.  In the next few pages, you will find information about Angelman Syndrome and how it has affected our lives.  You will also find out how you can help to raise awareness about this disorder and one day...FIND A CURE!!!


Please register (in the upper right hand corner) so that you can be added to our mailing list!    You will receive updates about Danielle and any current event information we may have about fundraisers.  Or, you can click on the contacts tab on the navigation bar and E-mail us.  We would love to hear your thoughts and ideas.  Thank You!


About Angelman Syndrome

In 1965, Dr. Harry Angelman first described three children with characteristics now known as Angelman Syndrome (AS). Through intensive genetic research in the 1980's, a defect in a small region of the maternal 15th chromosome was discovered as the cause of AS. In 1997 the specific gene, which characterizes AS, was pinpointed.

At present there is no cure. "Angels" are cognitively disabled and the development of speech is not likely. Typically, language consists of 4 to 5 indiscriminate words. Although rare, some have up to 20 words. While Angels cannot speak, they do have much to say. Angels suffer from significant movement or balance problems and 80% suffer from difficult to treat seizures. A short attention span and a happy demeanor make Angels behaviorally unique. With a normal life expectancy, Angels require 24 hour, life long care.*

*Text taken from Band of Angels information page.  A direct link can be found on our "Events" page.



Danielle and David's new Spring pictures




OUR NEWEST UPDATES...


2008 ASF PITTSBURGH WALK-A- THON

May 17

Please join us in supporting the Angelman Syndrome Foundation!  ASF holds a walk a thon every year to raise money for research. 

 We need your help! 

You can visit Danielle's online fundraising page to make a donation or register to walk with us in Pittsburgh.  We would love to see you there!  Danielle always has a large group of friends and family that come to support her!  There is always room for more! 

Thank you so much!  Hope to see you there!



 

Click on the above picture to go to my fundraising page!


Need directions to the walk a thon? 


Click here!




Angelman Syndrome Foundation, Inc.

www.angelman.org


Please visit this website!

  It has more in-depth information about Angelman Syndrome, medical information, and family support.

CLICK HERE!


*For a printable version of this site, configure your printer settings to landscape instead of portrait.*


Don't forget about the About Danielle Page and our Events Page!

Click below...

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