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owensmom
Posts:122
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Posted:06/04/2008 6:24 PM |
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I just got a call from Make a Wish and Owen's Wish has been approved by his doctors and plans are being made. We have chosen to go where Dreams come true.... DISNEY WORLD!!! Owen will love to see all the characters and go on the rides he will have such an amazing time. It's nice to have something good happen and to have something to look forward to besides a clear MRI. Owen is finishing his last week of school this week he has had such a wonderful time and I don't know what we are going to do next week when he starts chanting school school school....you get the picture.
To those of you who have been to Disney World or have been on a wish there have any ideas???
Cyndi (Owen's Mom)
www.caringbridge.org/visit/owenlyons
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mkees73
Posts:13
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Posted:06/04/2008 11:13 PM |
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Wonderful news, Cyndi! 
Do you belong to the Pediatric Brain Tumor Listserve on Yahoo? There have been a number of threads about Disney and Give Kids the World, where to go, what to do, insiders tips. Might be an idea for more information from families who have done MAW at Disney.
Michelle, m/o Andrew
www.carepages.com andrewpadfieldcarepage
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owensmom
Posts:122
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Posted:08/25/2008 2:31 PM |
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It is now 27 days until we leave for Owen's Make a Wish trip to Disney World. September 22-28. We will be staying at Give Kids the World. We will be there for a whole week. Owen is very excited to go to Mickey Mouse's House. We have had a rough summer with Owens surgery at the end of July, so what better way to start off the rest of Owen's life being cancer and seizure free then a trip to Disney World. This will be our first time to Disney World and if there are any tips or things we have to do, just leave me a note. We will be going with my sister and Owen's 2 cousins who are in 6th and 4th grade, so we want to have stuff for all of them to do. It should be fun. I'll keep you posted. I will be posting pictures on our dropshots page at www.dropshots.com/cyndi710
On another note, Owen is eating and drinking like he was before surgery. He is still a little weak and he is real sensitive to being around a lot of people. He is walking on his own again and will be back to our regular old Owen in no time.
Cyndi (Owen's Mom)
www.caringbridge.org/visit/owenlyons
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