A very quiet night......

We went to bed at midnight because he had to get his Pantamadine (spelling) which he must get once a month. This medicine helps prevent pnuemonia. He has to inhale the mist which is sometimes quite a chore. Besides getting up to go pee every two hours he did very well. We should be going home soon. If not today I would say tomorrow. Yesterday I mentioned about him having to learn to walk again. Well he put that worry to rest yesterday. Linda brought him a remote control car and Cody had it in the hall chasing all the nurses with it. He is a chip off the old block.... :D So much for worrying about walking...

Again, we are waiting for the results of his blood draw. They should be back around noon. We are hoping for a big jump from yesterday.

I would like to say "hello" to Sherry, Rob and their children Jenna and Brandon Will. They lost their daughter Ashlynne in December to neuroblastoma. Sherry, Rob and family have lived our nightmare and more. I hope they drop in and say "hi". My heart goes out to them... Diane and I were introduced to them by the fine people of ACCA. ACCA is an Air Conditioning Contractors Association that did a tremendous amout of work around our house when Cody was diagnosed the first time. They provided Christmas for the kids when Mom and Dad were busy dealing with Cody. We are forever indebted to them.

I will post more when I get more info....

I just spoke to Cody's nurse, Kelly. She said his numbers are at 470. She has to wait to ask the doctor if we can leave today. Technically speaking he must be at 500 but I think if they would do his blood again right now it would be 500. They draw blood at 4am so I know it is higher than 470 now. Cross your fingers....

1400 and we are HOME!!!!! He is playing Webkinz and chillin.... :D