While I was pregnant with my son, who is now 6 months old and has kallmans syndrome and x-linked ichthyosis, I was very often worried that he did not move enough. I even was sent to the hospital the day before he was born to get a non-stress test done because of his lack of movement. He seems to be making up for his lack of movement while I was pregnant now however because now he never stops moving.

Mom to:
Alex (xli and Kallmans - 2/3/05)
Liz (3/16/07)