Well tomorrow morning Stephanie comes home from camp. Shriners sponsers a
camp for SB every year and they finally convinced me to let Stephanie go.
It's been such a relaxing week for me. Ahhhhhhhhhhhhhh and now it's over.
I can't wait to go get Stephi tomorrow to find out all she's done. This
was her first time away from me for more then one night. I have to admit it
was so nice to not have to worry about cathing, meds, enemas etc for the
entire week but still know she is in the good hands of Shriners doctor and
nurses. But still I can't wait to get her back home!
Did you who have spina bifida go to SB camp? If so was it a good
Camp was always fun for me. South Carolina has a state run summer camp for
children with special needs. I also did the Scout Camp thing too.