Sunday, August 12, 2012

Children's Craniofacial Association Volunteer

I am so excited to be a part of the Children's Craniofacial Association! I have been following CCA Kids, as well as several of the children affected by craniofacial abnormalities, since Bella was born and recently applied to become a volunteer.

This weekend I recieved a box of goodies that will help me begin to raise awareness for craniofacial diseases, such as SMMCI Syndrome.


The Children's Craniofacial Association is a non profit organization located in Dallas, Texas that is commited to helping children, and their families, affected by craniofacial abnormalities. CCA addresses several concerns relating to children with craniofacial abnormalities, such as, medical, financial, pyschosocial, emotional and educational support.

To find out more information about the Children's Craniofacial Association, or to find out how you can help too, visit CCA Kids.

By the way, September is craniofacial acceptance month! Let's make sure these kids feel ACCEPTED, you can purchase bracletes, t-shirts, mugs and much more HERE to show your support throughout September, and the rest of the year :)


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