This question is for anyone on this board who is now an adult with CAH who was diagnosed early in childhood...   Could you please elaborate on your experience (physical & emotional) as you went through adolesence dealing with CAH?  My son is 13, beginning to be a teenager/young man and I’m curious about what to expect in the coming years.

Also, as an adult, how have your medications, check ups, etc. changed?  Are the meds different?

Thanks to anyone who wants to share their thoughts!