September 18, 2011
When my child got diagnosed with Craniosynostosis, we were terrified. Craniosynostosis and Positional Plagiocephely Support (CAPPS) had a great website and facebook page with tons of guidance and support. It really made things easier on our family going through surgery.
The Great!
I've personally experienced the results of this organization in...
The amount of support I found through CAPPS. I also received a beautiful blanket for my son's surgery and he will always treasure it.
Ways to make it better...
If I had to make changes to this organization, I would...
Have more events across the US
MY ROLE:
Client Served & CAPPS helped me with my own non-profit get off the ground with sending loving care packages to families facing surgery.