Hi members, I'm Sammie, I created this group in hopes of people who have children with CCAM's or are parents to be with a baby that has a CCAM to meet other people and discuss their worries, find information and get support etc. There is very little information available to some people across the world on CCAM's, I know when my I had the diagnosis at my 21 week scan in 2015, I wasn't told much about it, the information I did get was from a support group on Facebook. I wanted to find out as much as possible about it, and hear stories of other who have gone through it too. It can be a scary journey and so I hope this group proves useful. 

Thanks for reading!