I just wanted to say that since it was from my post that I had
mentioned about some delays of my son that we were just diagnosed
with CVS as of this past Thursday. His delays are more with not
opening his mouth when he speaks so others are able to understand
him. ALthough when he does want to speak he can. He has the
gripping of the crayon, pencil with a fist and I am working to show
him to hold it the right way. He has always had a lot of wax in his
ears and we think that might be part of the speech problem. We are
always cleaning them out and the dr. is informed of this. I had
read some info about CVS on the net and when reading it (i misread)
about the light and the withdrawl. He is a very shy person and is
easliy embaressed. When I read (what I misread) I thought it said
that children with CVS are withdrawn all the time not just with an
episode about to happen or durning one. After Susan sent me that
message I went back to the site and re-read what it said. I was
wrong. I am sorry if I caused any problems with this. Like I said
I am new to finding out what my son has and while reading what I
did - I was just so happy that there is a name to what has been
happening to my son and I got a little excited. Again - I am truely
sorry for any problems that I may have caused.

Rebecca