making strides

Cameron is lieterally making strides (walking more steps) each day.  As of today he is a Rehab patient instead of a neurology patient.  YEAH!!  

Cam has an intense 3 hours of Physical and occupational therapy everyday but is having fun and getting stronger. 
His personality has 100% returned and most of the time I am loving it. There are exceptions like when he sprays me with the shower hose right before I am going out for a date with Mark!  Or when he yells at me just like he used to do at home!  Among other little Cameron quirks!    I will admit that when it was time to turn him over to Mark last night I was looking forward to the 15 hour break, he's quite the handful!
It is fun though to see him interact with all of the nurses and therapists. They think he is pretty great and laugh at him most of the day. 
At this point he is so close to being able to walk without assistance, it's amazing. 
He was truly blessed.

Thanks again to all of our GREAT family and friends that have helped us out and visited us.  Having never been on the recieving end of all the help I am feeling totally inadequate at being able to thank everyone enough.  

from primary childrens hospital

(picture of strength)

Well, here we are in the hospital, for how long we don't know. They have said at least a couple of weeks, but I know that Cam is going to get better quicker than the doctors think, he's STRONG like that! For now though he thinks he is going to starve to death because they won't let him eat until after all the tests tomorrow. I keep telling him to be brave and that we brought him to the hospital to get better. He got mad at me and said, "you brought me here to starve me to death!" Feisty strong 5 year old he still is. He is going to set new standards of strength for this Guillain Barre Syndrome.