We have also started the process of getting her Early Intervention(EI). I have already filled out the paperwork and Tuesday we see the therapist for an evaluation. It is nice to have a program that will help Delilah with her development. We still see her occupational therapist, Sally, every Wednesday. She is wonderful. I hope the therapist with EI is just as good. Our case manager said she has worked with several other PWS children a few years ago.
We are also working on getting in to see an Endocrinologist Pediatrician. According to all the information about PWS, the Growth Hormone Therapy is the best way to go. Seeing how I don't really understand all the medical lingo I have read, I really want to talk to a doctor who can spell it out in plain english for me. Many of the other parents I speak to on a PWS message board boast about how well it helped their babies.
Well, I have gone on long enough. It is off to play with Delilah, feed her, then bed. Good night!