This blog tracks our family's day to day life while battling our son's diagnosis of Infantile Spasms. Feel free to follow us as we continue to fight against the seizures and devastating effects of this terrifying form of epilepsy. You may also read Austin's full story at the bottom of the page.
Wednesday, October 14, 2009
This is what keeps me pushing through. Because beneath the medication, I sometimes see this side of him. And it reminds me that this is the way he should be.
By the way, I cannot figure out why all my photos are coming out orange-ish. There's no telling what I've done to my camera!