I know I promised some of you that I would update the blog with information as to how Henry is fairing. He remains in hospital and we are hopeful that he will be well enough to be home by the weekend.
The challenge for him, now that they have treated the pneumonia, is keeping his oxygen saturation levels up. He has trouble getting around and requires oxygen at all times and also the use of a Nebulizer at prescribed intervals. He is getting physical therapy to keep his muscle strength up and to loosen the mucous in his lungs. Because the kind of pneumonia he had was "aspiration pneumonia" he remains at risk of it reoccurring. Any excess fluid in the airways or food that gets trapped in the throat can put him at risk.
Christena is anxious to get him home. We have made the calls necessary to arrange for nursing care to come into the home when he comes back. She is looking forward to the help and to learn whatever tips and techniques they can offer which may make the adjustment easier for all of us.
Jennifer came back to Ontario to see Henry and spend some time with him in the hospital. While he is improving from his most recent health scare we are seeing significant changes to his memory and she was hoping to see him and have him know who she is. He has changes dramatically since Christmas even. As I am sure you can imagine, it is difficult to wrap your head around the idea that someone you love so much may not remember you one day. This is truly a horrible disease.
We appreciate the prayers, vibes, words of encouragement, etc. that many of you have sent. Thank you for keeping Henry in the light.
Tuesday, January 30, 2007
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