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Your Voices: Sarah's Story

My name is Scott and my daughter, Sarah, has a mild case of CdLS and this is a little about us: Sarah was diagnosed around 1 1/2 to 2 years old. I thought it was a death sentence at first because I had never heard of it before. Little did I know it was far from it, especially with her turning six this April. Has it been challenging? Of course it has, but it also...

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CdLS Foundation Leadership Structure

Learn more about how the CdLS Foundation and our leadership structure (click the image to view full size version):...

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