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
Sunday, June 2, 2013
Saturday, June 1, 2013
One more week...
Well, the end is in sight...
We've been teasing him that his "Twins" casts have been certainly bringing the team good luck (his latest pair of casts are red/blue...aka Twins casts) and that we might have to consider keeping them on until the end of the season...somehow Ethan doesn't seem to be very receptive to that idea. Nevertheless next week Monday, they come off...and we can proceed with "next steps"... Yeahhhh!
School was out for summer vacation on May 23rd and all three of the kids were more than ready for a break and for some warm, sunny weather. We are all truly excited to see what his summer has in store for everyone.
That's about it for now...
Until later,
Lisa
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