Just finished at our 15-month well child visit for DD. We brought up our concerns about her loss of words/signs, bowing of legs, turning out of feet, gagging while eating, lack of rolling over (still.), inability to follow a simple command ("pick up the book"), and favoring of her left side. Our pediatrician shared our concern of CP and put in the referral for a pediatric neurologist.
I am feeling all sorts of things right now. I'm happy and relieved that our concern was heard and acknowledged and not just brushed off. I'm also a bit scared. The pedi used the term "borderline global delays." We're in the process of adopting DD, so neither of us carried her for 9 months, nor knew her before she was 2 months old. But the thought "could we have done something differently?" is still crossing my mind. I'm also very sad for her. I'm sad that she is struggling to the point where it is delaying things.