Good morning, Everyone!
It has been a lovely weekend and I was able to take my beloved husband out for a wheelchair ride. He does so enjoy being able to be outdoors. He is in probably the final stages of CBD. His speech has recently become mostly slurred yes and no. His right side is now, for all intents and purposes seemingly paralyzed. He can move only with extreme effort and usually with the help of his left arm. Our hospice nurses are so helpful and kind but no one can see the subtle changes I see, sometimes everyday. One increasing change is that his eyes water almost constantly and he appears to not be able to see where things are in space. He will reach for something and is nowhere near where the object is. He is also increasingly easily agitated. Has anyone else experienced these things as the disease progresses?