hello. i have and infant son with swcah. he has had problems with growth and several crises due to viruses. we live in a rural area with only one peds endo and no nearby medical university. i am wondering if we should relocate to an area where research is being done, there is a higher population of people with cah ( my son is the only one in the practice with it), and there are more experienced docs in the area. we dont have a  lot of family where we live, so i would not be missing out on that and my husband and myself have jobs that would make relocation pretty feasible. however, i wonder if i am somewhat over0-reacting. just wanted others opinions. has anyone out there ever relocated for better access to medical care for their cah child??

thanks

theresa