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.
Tuesday, May 26, 2009
Thinking of Sophie
My heart and mind are on Sophie today as she should be undergoing the first part of surgery -probably as I type.
Please keep this little one in your thoughts and prayers.
She so deserves this to be her miracle!
(Any of you unfamiliar, you can read this or this)