Jonathan completed physical therapy for torticollis in April and saw some improvement in his head shape. From March 3 to April 22, his cephalic ratio decreased from 92.3% to 87.1%. His asymmetry remained 16mm, so we decided to go ahead with a helmet.
We've had quite the time getting an appointment with a neurosurgeon -- even in a big city like Houston. One specialist's wait was until September! Our pediatrician finally wrote the script herself, and Jonathan was fitted for a STARband last week. We received the helmet on Thursday, and Jonathan has been progressing on the wearing schedule.
Last night was his first time to wear it through the night, and he did so well -- he didn't wake up at all. I really hope last night wasn't a fluke. *crossing fingers*
We've been out to IHOP and a mall while wearing the helmet -- no snide comments yet. We've had quite a few looks and even a few pointing fingers, though.
Otherwise, I know Jonathan is unaffected, and I'm fairly okay, too. Decorating with stickers really did help the helmet seems less medical. And after seeing him wear it for increasing amounts of time, his head seems so small and weird and naked without it. Strange, huh?