Jay woke up at about 4.00am but went back to sleep on and off until about 7.30am, we got up and Jay had his breakfast, then we went to the computer room (for a change). Jay went to physio, he worked quite hard for Mandy. He also did ok for Lilly his OT, he didn’t want to lie down for his massage. Jay isn’t doing as good in his therapies as he was before the stem cell injection which is a shame. I hope he doesn’t get as ill for the next injection. Granny and Julia went to the supermarket.
We have booked a hotel for 3 nights to give us all a break, one person will stay in the hospital and the other 2 will go to the hotel, then we will swap over, we all get 2 nights each in the hotel, I cant wait. It’s me and Julia that go to the hotel tomorrow (how exited are we).
November 30th, 2007
Jay woke at 7.15am this morning and he feels much better, he had some juice and 2 bowls of cereal. Julia took him to the computer room and he was much happier, he didn’t want to lie down, so his head must be much better. Jay went to PT at 9.30am to see Mandy, Julia took him and said she was very surprised to see that Jay was doing so well, as this was the first day of him doing any exercises since his stem cell injection (Thursday). He took off his shoes with a little help, and he lay down so Mandy could exercise his legs and back, we bribed a little with some sweets, it helped. He did well for his first day after being so ill. When we had finished Julia took him to the computer room as he loves to get out of our room. After that Jay came back to the room and he had a sleep. Jay went to OT at 1.00pm, he didn’t do much for Lilly and he had TCM at 4pm, he was very good for this. It’s good to see Jay feeling a lot better.
November 30th, 2007
