I had a phone call from Dads care home today to say dads choking was getting worse to the point they had to give him back slaps. The nurse examined him and said he had crackles on his lung. The GP was then called she told the care home there was nothing to do as he could not take the antibiotics and they were looking at end of life. The home called me as they were concerned the GP hadn't discussed this with me. This came as a bit of a bolt out of the blue as although Dad has a DNR we had not considered the choice of sending him to hospital to be put on a drip, to be in a unfamiliar place, to perhaps rally round to return to choking on his food or to allow him to stay in the home who are still attempting fluids and will care for him in familiar surroundings. But the fear is there of making the wrong choice. Dad is 89 and very frail.
After the initial shock and discussing with family, home and GP I have decided he will stay at the care home but I just hope I have made the right decision for him. The last thing I want for him is to suffer but I don't see the benefit in trying to prolong his life for our own feelings. He has no quality of life left but I am sad he has come this far and I have had to make this difficult choice for him and that he didn't go peacefully in his sleep. I'm not sure people that have no understanding of dementia will understand my decision.
After the initial shock and discussing with family, home and GP I have decided he will stay at the care home but I just hope I have made the right decision for him. The last thing I want for him is to suffer but I don't see the benefit in trying to prolong his life for our own feelings. He has no quality of life left but I am sad he has come this far and I have had to make this difficult choice for him and that he didn't go peacefully in his sleep. I'm not sure people that have no understanding of dementia will understand my decision.