Just thought I'd share the news that a photo of my son Roman was chosen to be on the cover of CAPPSKIDS new brochure about craniosynostosis!
They will be distributed to neurosurgeon/crainiofacial centers, health fairs, and pediatricians offices around the country. Yeah for awareness!
I wish your craniokids website could be on the brochure too, since the support here really helped me, but as far as non-profit organizations go, www.cappskids.org is great (they sent him a free blanket, etc.).
See pics of the brochure in my photo album.
Such a lovely surprise. It's nice to think that somewhere someday someone is going to pick up that brochure and see the photo of my son and the other babies and read about cranio, that could lead to an early diagnosis for their child and put them on the road to surgery and recovery and healing. Feels good to be able to "pay it forward" in some small way.