Alexa's Craniofacial ​​
Awareness Charity Event

Benefitting...

Children's Craniofacial Association

  
Each year more than 100,000 children are born with a craniofacial condition.  These same children are among the least accepted and understood in society.  We want to change that and are asking for your help. 

We are proud to be the organizers of Alexa’s Craniofacial Awareness Dinner; a charity dinner to benefit Children’s Craniofacial Association, or CCA (www.ccakids.org).  CCA is a 501(c)3 non-profit organization that helps families with the financial burden that comes along with having a child born with a Craniofacial Anomaly. These needs include surgery and travel expenses. CCA provides much needed financial and emotional support to families worldwide.  They also put on an Annual Family Retreat & Educational Symposium.  

  This retreat is LIFE CHANGING and reaches hundreds of families per year, and growing!! These Family Retreats are a special time for these children who stand out for reasons they want to hide.  One time a year they are guaranteed to feel “normal”.  They are surrounded by others who feel the same way.  They are seen for who they are, not what they look like.  The friendship and bonds built between these children is priceless.  The support we get as parents from other parents who attend, dealing with the same struggles we do, it absolutely what keeps us strong.  No words can do justice to what these Family Retreats mean to us.  Unfortunately so many families are not able to attend due to financial hardships from the medical needs of their child.  CCA has scholarships to send families to the retreats.  We are raising money for these scholarships to send more families to the Annual Family Retreat.  It costs $1000. to send one family.  Come and meet some of the CCA kids and their families!
  
  
CCA is a charitable non-profit organization that benefits families all over the world, as well as locally here in the Central Valley area. These funds will help provide assistance to children and families wherever needed.  CCA was a great resource for our family in 2007, when Alexa was born, and we want to help ensure others are aware of this great organization and their willingness to assist families in our community.  Their support is not limited to children born with facial differences; in fact they assist children who may have suffered a trauma that has left them facially disfigured such as cancer, an accident, or dog attack.
  
  
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