In Sepetember, 2010, we will be taking our son, Zane, to Germany for an autologus stem cell treatment. We are very excited to see how this will help improve the symptoms he has from cerebral palsy, spastic quadriplega! More information regarding the treatment and ways to donate to our fund can be found on his website at www.awayforzane.com!
Saturday, September 25, 2010
WE MADE IT!!!
We have arrived in Dusseldorf! We came straight to our hotel room after we got off the plane so we haven't been out doing much yet. So far we love it here. Our hotel room is SO nice! When we got off the plane, someone from the XCell Center was waiting to bring us to our hotel. (Which is right by the airport!) I wasn't expecting them to be there so that was a nice suprise. Zane is playing in the floor with his cars and Jeff is trying to find English channels on the TV. We have to report to the XCell Center on Monday at 2:00 pm for our anesthesia consult. The bone marrow aspiration is Tuesday and the lumbar puncture is Wednesdays. As soon as I have specific times I will post them. Germany is 7 hours ahead of the time back home. I'm hoping to get off here and catch a nap, so I will be updating as we can! Thanks for checking in!
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