I'm not even sure where to begin....
We've started some PT for William and added some OT and PT from ECI as well. Much more time and energy to devote to helping him get better, yes BETTER.
I've learned that the chance for recovery is greatest in the first 6 months (we're at 5 months now) and continues to be high in the first 18 months, after that the injury will not improve much, but won't get worse either. I've asked a great deal of questions and met with several new people, and they all think William WILL LEARN TO WALK!!!!, but part of the key is to get his as much therapy as we can....NOW, and also working with him as much as we can.
We've been shown new exercises, and were trying to do them as much as we can, I've got some photos on my phone to explain, and I'm hoping to make a big chart for the wall to put photos and explanation in to remind us of exercises to do.
I've also been given some ideas of some other therapies to check into, HBOT, and also check into getting him services from Texas Scottish Rite Hospital, according to their web site he appears to qualify, so I will call them tomorrow to check on it. There neurologists see more kids with Cerebral Palsy, where as the neurologist he sees already sees more kids with epilepsy. Maybe there's another medication that's better or that can lower his Valium dose. Or the possibility of better therapies etc.
4 months ago