Hi! I am new to this sight. I have 2 children (daughters) a 7 year old and a almost 2 year old (who has sw cah). I have a few concerns and questions for other parents of children with cah. My daughter (with cah) is going to be 2 years old on friday. She is only 27 inches and wieghs only 18 pounds she is very tiny, She wears 12 mo. clothing. She is fairly healthy, she takes cortef (3x daily) and florinef 2x daily). She is on target otherwise, just not in size. Is this normal? She has had bone age testing and other things, and her endo said she was fine, her meds have been changed a few times, she is starting to grow some. Is she always going to be shorter than most kids? She is way behind of what her sister was at that age. Is it her meds or her or is this just what happens with cah children? My daughter doesn’t talk much either, she is starting to do better, I wonder if that has to do with cah? I have so many questions, I just can’t think of them all. I love this sight, Some of my questions have already been answered by reading the posts, but I just want to know how things are going to be as she gets older, anything I should watch for or be prepared for? Any help or advice would be greatly appreciated. I was so overwhelmed when she was born and diagnosed and during her surgeries that I didn’t know what to do, but in the last 2 years I have tried to educate myself and learn whatever I can. Any words of wisdom or advise will be welcome with an open mind and thankful heart. - Thanks- Michelle