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.
Here is a video montage I put together of Colin's entire first year. He's 17 months old already and I can hardly believe it. My baby is not a baby anymore. I have thoroughly enjoyed each and every moment!
