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The blog was developed for our family and friends and for our extended Angelman Syndrome family. We hope you enjoy keeping up on the episodes of the Evans family. There are useful links and plenty of blogs and videos on AS for anyone looking for more information. You might have to look at older posts in the archives to find pictures and videos of Chance. Feel free to email Heather directly at heather.a.evans@comcast.net if you want any information on Angelman Syndrome.
1 comment:
You have a beautiful family and I just happend to stumble across you as I was looking for others in the Martinsburg area. Thank you for sharing your blog out there in the "cyber" world, because it opened my eyes to something that I was not as educated as I would like to be as a special educator. Thank you!
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