We have been members of the Magic Foundation since our son was diagnosed with CAH in 1998. When Jordan was born, in Northern Ontario, Canada, we had no information about CAH at all, and even our doctors had nothing to give us. Almost everything we know has come from the Magic Foundation, and its newsletters. We are planning to attend the conference next July, because we have heard it is a great source of information and support. The director of the CAH division of Magic, Kathy Kusch, has been great at giving us advice and help when we have had problems - she even spent one hour talking to my husband on the phone answering all our questions. We really recommend support of this wonderful organization!