I've been getting a steady trickle of emails from people who have had a child either diagnosed or put on a watch list for craniosynostosis. So, in the next few weeks, I'm going to dredge together the common questions I've been getting, and tag them all together.
So, THAT'S a project and a half. But--I am so grateful for the random internet strangers who did the same for me. As I told someone else today, the only way I can pay it back is to pay it forward.