Archive for December 15th, 2007
Jays last day of IV today, he will be happy, no more lying about for hours. Jay is very well just a bit grumpy but so are the rest of us. We are taking Jay out tonight to see an acrobat show, I think he deserves to get out after all he has been through. We have started to pack, we are all struggling to get everything in our cases after buying our christmas presents.We have met some really nice people here, some people are so kind.
Only 2 more sleeps until we come home.
Thanks to Cheryl, Sam, Gemma, Carly and the kids at the Out of School Club for Jays Christmas card, he received it the other day.
December 15th, 2007
We are now near the end of our stay, this is the last day of Jays therapies. We went to physio with Mandy, as normal Jay didn’t want to co-operate, Grandma came along to camcorder the exercises so we can carry them out when we get home. We did the same for OT and for TCM. Jay has really had enough now and is ready for home, he can’t be bothered doing any exercises and is getting a bit naughty at times. We are all very tired and I just want my own bed, only 3 more days and counting. This has been an experience I wont forget, lets hope the stem cells grow over the next 6 months as they are supposed to. The Doctor said they are like seeds and the medication Jay has to take will help them grow. Also seeing how some people live here, we don’t know how lucky we are.
December 15th, 2007
Jay in good mood today. Jay missed PT but went to OT and TCM. Jay seemed to use his voice more today, trying hard to pronounce words. He repeated three times after Lily saying ‘say Hi’ very clearly, you can imagine the joy Lily and Grandma felt when he said it not only once but three times. Nicola and Julia are away to the Silk Market to check the new suit Nicola is having made. Jay fell asleep at 7.00pm not sure if he is down for the night, he may waken and be full of life later (hope not).
December 15th, 2007
