So great to find this forum. It is definitely unique having a child with special needs within a triplet group. It certainly has its good points and bad. I have 21 month old ggb triplets born at 32 weeks on the nose. Sydney and Jake are "typical". Molly has cerebral palsy. Molly had severe reflux until at 10 months she had the nissen fundoplication surgery. It was the best decision we ever made. She could not sit up by herself before the surgery and sat independently 2 days after surgery. Molly is not walking yet but can pull up and cruise. She is a beautiful fast crawler. She is speech delayed but is babbling a lot now. She signs "more" but not on a consistent basis. She says "mama" and told her speech therapist "bye bye" yesterday for the first time. She is my greatest sorrow and my greatest joy!