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!

Friday, October 1, 2010

Just a day of relaxing...

Today we have spent the day relaxing in the hotel. Zane has been playing with his cars and watching movies. He has been acting totally normal and hasn't been in any pain at all today. So far, it seems as though Zane's left hand is A LOT looser than it was before. He is actually using it to help play with his cars. Normally he keeps it fisted up. Last night he had a car in both hands. This is a HUGE improvement. Today, when he was asking for a drink, he said "da-rink," normally he says "dink." These may seem like small improvements but even the smallest thing can change Zane's quality of life. We are expecting to see more improvements in the next several days/weeks/months! We have had a great time here, but we are ready to come home! Tomorrow will be a long day as we start our journey by arriving at the airport at 7 am (midnight back home) Our flight will land in St. Louis at 4:30 pm tomorrow afternoon. We are so excited to see our family! Dean and Rhonda and Ezekiel will be picking us up at the airport! We have missed him SOO much! We are planning on eating dinner (McDonalds again) and getting to bed early so we can get some rest for our big day! We are all packed up and ready to go! Thanks again to all of you who have supported us before, during and after this trip! God Bless you all!

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