Tuesday, April 26, 2011

Welcome to the CCA Kids Blog!

Welcome to the CCA Kids Blog. If you're coming across this page you or a family member are most likely affected in some way by a craniofacial condition. You may or may not already be familiar with Children's Craniofacial Association - a 501(c)3 nonprofit organization that is dedicated to empowering and giving hope to families and individuals affected by facial differences.

As a parent of a child with Apert Syndrome, I have partnered with CCA to create this blog and with the help of other craniofacial families, CCA staffers, and board members, we plan on sharing personal stories, reflections, and experiences. In addition, as time goes on, we will continue to add updated information and resources for all things related to craniofacial conditions.

The CCA Kids Blog is intended for anyone interested in learning more about craniofacial conditions, but most of all, for families who have a child or loved one affected by facial difference. If you are just starting out on your craniofacial journey, be sure to visit CCA's website: www.ccakids.org for a more comprehensive look at ways they may be able to help you along the way. No matter what stage of the journey you are in, we hope you will find this blog to be a welcoming, informative, and inspirational place.

Visit the links below to read more about this blog and to meet the CCA Kids Blog contributors.

1 comment:

  1. Great idea and I think it will be a great tool for new families!


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