I can imagine that my FIL thinks on these things quite often. I wonder if it would make him feel better or worse to hear these words. He can’t read them, as he is blind. He can’t walk either, but I think it’s his eyesight that he misses most.
It’s kind of sad in a way that doctors and meds can keep people alive for so long at the end of their life in some situations. He’s been on hospice now for over two years. He sleeps for more than 20 hours a day. He does enjoy eating a good meal and listening to music, but he doesn’t even eat much lately.
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