I was wondering if any of you out there have CAH children involved in the NIH study. We live in Baltimore, Maryland so we are very close to the institute and many people we run into suggest we check it out. I have some info about what is being done, but I can't find anything that suggests whether or not this new treatment has been successful. We have a lot of concerns and questions, and although we are probably not interested, any info you might have would be greatly appreciated.