My daughter was born in 1991 before there was a CHERUBS I would have loved this support then but it has been there for me even 21 years down the road. Having a child with CDH is like walking on the moon i never met another CDH parent until CHERUBS. This group does wonders from hearing the words I'M sorry your child has CDH to what do you need forever. Thee fact that half these babies is a shame they get very little funding and never enough help.