One of the challenges faced by Care Givers of dear family members who develop Memory Loss is finding it almost impossible to know where to start. It is a sort of paralysis resulting from the shock at finding the menace in ones own household.
This blog is based on personal experience over the last two years of 2012-2014. The purpose is to experiment to find the best way for one person to communicate about an experience that is unique and different in every situation. The complexity discourage words but without words there is no way to share mutual experience both to comfort and to inform.
My spouse is presently in a fine group home.
I will be adding more blogs as seems wise. The Care Giver experience is often fatal because of the constant need to be alert because of caring so deeply for your mate. More on that later.
This blog is based on personal experience over the last two years of 2012-2014. The purpose is to experiment to find the best way for one person to communicate about an experience that is unique and different in every situation. The complexity discourage words but without words there is no way to share mutual experience both to comfort and to inform.
My spouse is presently in a fine group home.
I will be adding more blogs as seems wise. The Care Giver experience is often fatal because of the constant need to be alert because of caring so deeply for your mate. More on that later.
