Five people have found my blog by searching Cerebrocostomandibular Syndrome in the last month. Now, I'm not sure if they are people who know me who just couldn't remember the blog address, or if they are people who need to find out more information about the syndrome. I'm hoping it's the latter because I really do want to connect with people whose children have CCMS. If you are reading this and your child has been diagnosed, PLEASE email me! I would love to talk with you.
From time to time, I'll do a post with the title of Cerebrocostomandibular Syndrome so that it will show up in Google if someone searches for the syndrome. Between my blog and Reagan's, we just want people to know that there are real families out there dealing with CCMS!