My son Ethan has Cerebral Palsy-spastic diplegia.In July 2010 we had an adult stem cell treatment in hopes that our son would get his wish of having as he puts it "New Legs that Work". This blog is our story, adventure and progress.
A WORD TO READERS:
This Blog is intended to educate as many as possible. Our story is unique as is each story of a special needs child.
Thank you!
Lisa
Thank you!
Lisa
Wednesday, May 2, 2012
The day after surgery
Ethan is doing ok...not bad but not great. He's in a considerable amount of pain as to be expected but is also struggling with painful muscle spasms. The staff here has been top notch and we cannot complain at all. Right now the plan is to remove the epidermal tomorrow and to give him pain meds via the IV alone. In addition, he'll likely get casts on tomorrow as well as a removable stabilizing bar. He's making progress and the bumps we're seeing are typical...nevertheless it's never fun to see your little one in pain of any kind. Right now our predicted discharge date is Saturday.
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