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Cornelia de Lange Syndrome Foundation, Inc.
November 28, 2012

When it was suspected that our daughter, now 4-years old, had CdLS, we found comfort in knowing the Foundation was a resource for us. This past summer we attended our first CdLS conference hosted by the Foundation. Whatever hesitancy we felt melted away within the first few moments of stepping inside the door. Whether it was meeting other CdLS families, speaking with physicians or therapists, or simply watching our daughter interact with her new friends, we could not have felt more embraced or at home. The staff and professionals associated with the CdLS Foundation are an amazing and inspiring group truly dedicated to championing for families.

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How do you feel you were treated by this organization?

Very Well

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Client Served

February 17, 2010

The museum is a wonderful place for children to explore their environment. Given we live in the Midwest, snow is easy to come by in the winter. It's wonderful to bring the children to a place that's always 70 degrees and sunny inside. Also, as a parent of a special needs toddler, the Museum is ideal of introducing kids to a variety of toys and activities that enhance fine and gross motor skills, as well as interaction with other children.


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I've personally experienced the results of this organization in...

seeing first-hand the joy on my children's faces when we enter the museum. It's a place of wonder and amazement.

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About every month

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General Member of the Public & Take my children to museum.