As Apert Awareness month comes to an end I wanted to share this video of our first Craniofacial Awareness picnic our family put together. Awareness is very important, especially for our kids. For this first picnic we met new families, Cargill really helped us out alot with donated food, and we had a walk at a park. it was small but it connected us, we had such support from family who came down from Dallas, and friends who traveled to attend. This was our start, as you have seen, cause I have filled your newsfeed with pictures and videos, Childrens Craniofacial Association is a big organization in our life. September is another month we focus hard on raising awareness for all people with facial differences. Once we build our network in this town we hope to continue the September community picnics to raise awareness for Salem and others with facial differences. Its not just June or September, its everyday we hope to reach at least one person and teach them about our son and the importance of accepting him and others no matter their differences. Please help us teach the world, this month you have learned about Apert Syndrome, teach your children that its okay to ask questions, but always choose kind, reach out to others, stand up for those who are being bullied for their differences. We want to change the world for our son, if one person at a time, but we will always teach him that he is a beautiful person who can do whatever he dreams of doing, and to never let anyone break his spirit.
Posted on: Tue, 01 Jul 2014 02:40:33 +0000
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