I can't believe how long it's been since I last updated. I'm sorry about that!
As many of you know, Dad spent 13 days at Kobacker House and was sent home early for good behavior (my words, not theirs). He was feeling well, eating like a horse and not Kobacker material. The doctors felt he wasn't "actively dying" and he got to transfer home under continued hospice care. I think it was a great treat for Dad to be in his own home and in familiar surroundings after more than 9 weeks straight in a hospital facility.
However, Dad is now returning to Kobacker. He's been dealing with an increasing level of pain and it is simply too much to be managed at home. The hospice nurse suggested returning and Dad agreed it is the right thing to do. So, this afternoon he'll be heading back to Kobacker after a week long vacation at home.
We thank you all for your continued love and support. At this time, due to Dad's ever increasing level of discomfort and need to rest (and to respect Kobacker House) we ask for limited visits. It's best to call ahead before stopping by.
Showing posts with label comfort care. Show all posts
Showing posts with label comfort care. Show all posts
Wednesday, May 4, 2011
Wednesday, April 13, 2011
Kobacker House
Dad has been transferred to Kobacker House. It is a small inpatient hospice care center with an excellent reputation. We were very hopeful he would go here and are thankful the transfer was arranged so quickly and that they had a bed available for him.
Today was very bittersweet. Dad spent most of the day (and last night) sleeping peacefully. They stopped waking him to take vitals so he got his first full night's rest in, literally, nine weeks. But, there was a period this evening when he was wide awake and very lucid and had us all laughing hysterically. I hope everyone who cares for Dad has a moment like that with him.
Throughout the day and last night many nurses and PCAs stopped in to goodbye to dad and to say really nice things about him/ how much they enjoyed him. It was nice to see how they had grown to care for dad - nurses rearranged schedules to see him, they fought over who would care for him and even came in on their days off to say good bye. He really did receive great care at the James and we're grateful for all they did for him.
Here's the address for the Kobacker House, should you need it.
Thanks again for your continued love and support.
Today was very bittersweet. Dad spent most of the day (and last night) sleeping peacefully. They stopped waking him to take vitals so he got his first full night's rest in, literally, nine weeks. But, there was a period this evening when he was wide awake and very lucid and had us all laughing hysterically. I hope everyone who cares for Dad has a moment like that with him.
Throughout the day and last night many nurses and PCAs stopped in to goodbye to dad and to say really nice things about him/ how much they enjoyed him. It was nice to see how they had grown to care for dad - nurses rearranged schedules to see him, they fought over who would care for him and even came in on their days off to say good bye. He really did receive great care at the James and we're grateful for all they did for him.
Here's the address for the Kobacker House, should you need it.
Thanks again for your continued love and support.
Tuesday, April 12, 2011
April 12 Update
Things can change in an instant. They sure did for all of us when we heard dad had AML. And, they did again today when we heard that the leukemia has again spread to dad's bloodstream. If you remember, his post-chemo bone marrow biopsy showed leukemia cells still in his marrow. Since then, the leukemia has done its dirty work and spread. Dad's blood counts had decreased over the last week, but yesterday was the first time they noticed an indication of leukemia in the blood.
If dad were well enough, the doctors would recommend the next course of treatment - chemo, bone marrow transplant - but he is not. He's still quite ill and they can't seem to fix him. It seems that perhaps parts of his body are done fighting before we expected.
The entire family (sans Jon) gathered in the hospital room with dad to hear the options from the doctor. After hearing the grim reality of the situation - that, given his type of AML a chance of achieving remission from chemo is around 20% and with a transplant is around 40% - and the fact that there is no possibility of such treatment any time in the near future because he's ill, Dad has decided to change the focus of his care to hospice care.
We support and completely understand the decision. Tomorrow they'll start the process of moving him to a hospice facility and in the mean time will change his care to focus on comfort and not treatment.
It's obviously a difficult time for all of us. I'll update when we know where he'll be staying.
If dad were well enough, the doctors would recommend the next course of treatment - chemo, bone marrow transplant - but he is not. He's still quite ill and they can't seem to fix him. It seems that perhaps parts of his body are done fighting before we expected.
The entire family (sans Jon) gathered in the hospital room with dad to hear the options from the doctor. After hearing the grim reality of the situation - that, given his type of AML a chance of achieving remission from chemo is around 20% and with a transplant is around 40% - and the fact that there is no possibility of such treatment any time in the near future because he's ill, Dad has decided to change the focus of his care to hospice care.
We support and completely understand the decision. Tomorrow they'll start the process of moving him to a hospice facility and in the mean time will change his care to focus on comfort and not treatment.
It's obviously a difficult time for all of us. I'll update when we know where he'll be staying.
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