I agree, more research and money should be spent in improving treatment and ultimately finding a cure for CAH, rather than wasting precious resources trying to discover whether carriers have symptoms.   Depression, high blood pressure etc are common conditions and can be caused by life style, stress or genetics and it cannot be assumed that these are factors of the CAH carrier status.   I know my son is one of the lucky ones who responds well to the treatment and has received excellent care, especially in recent years but I am always sad to read of others, such as Mary’s son, who has obviously had a hard time.  Better understanding and universal good treatment and care should be a priority when it comes to research into anything to do with CAH!