02/04/12

We are getting into a routine at the hospital as Jules continues taking small steps forward.  Monday was another good day she was off the ventilator for 17 hours and was only connected whilst sleeping at night.  The nurses are letting her use the speaking valve as she wishes on the understanding that if she tires she will tell them so they can remove it. Margie and I did three rounds of physio on her biceps and triceps.  Her lungs are improving and the need for suction in reducing.  I think that when she can go without the ventilator for a few days straight they will consider removing the tracheostomy which will be a real milestone.

Dr Vernon Hill and Dr Polly Tie from the spinal unit stopped by for a chat with Jules and I think to gauge her progress to get an idea when she will be ready to transfer to them.

 Larissa and Celeste are providing food for some meals and Jules is enjoying this.  She is eating a normal diet with plenty of fruit and fresh fruit juice and enjoying it.  You could never call the hospital food "normal" in any sense of the word.  I wonder how people without family and friends to visit and bring food survive.  Visitation is so important for morale.

 Yesterday Kylie forwarded the photos of Jules before, during, and after the hair cut.  You will see from the pics how good she looks, she isn't sick at all but a healthy person with a spinal injury.  Today Val has arranged for her to have a manicure and pedicure she is looking forward to this.  If possible we will get her to the balcony for a few hours today.

 Today again clinically there is not much to report which is good news.

 Kind regards Norm