Max has done really well on the cannula oxygen....it is SO nice to actually be able to see his little face without all the head gear and tape. He still has a feeding tube which is taped to his chin......but we can see MOST of his face. He is allowed to be on the cannula for up to 6 hours a day depending on how well he tolerates it. The rest of the day he is still on the C-Pap. Alissa is really enjoying being able to hold him and play with him without quite so many tubes and wires to worry about.
I havent't held him without the C-Pap yet....but I am looking forward to it. I think he is almost smiling....he, too, likes being FREE...or at least freeER!!
I havent't held him without the C-Pap yet....but I am looking forward to it. I think he is almost smiling....he, too, likes being FREE...or at least freeER!!
1 comment:
Karen:
I have followed your two Grand cruises and am now following Max. I applaud you for the joy you live your life with and the great faith you have. Max is in my prayers every night. I hope to meet you on a HAL cruise some day.
Post a Comment