This is transcript and video Link for second of four quadrants from my speech.
I have been very busy with my Service Dog trainee, Dementia Mentors, Dementia Action Alliance, and Dementia Chats. But just because I have no recent blog entry postings does not mean there is nothing new to read from Truthful Loving Kindness. “About Me” has recently been revised at https://truthfulkindness.com/about/ . 47 “Other Contributors” are available at […]
Kate Swaffer comment got me thinking about quotes to live by, which motivated these thoughts about living in the moment.
This year’s changes in Holiday celebration.
Be willing to invest NOW in learning communication skills for the later stages, so that you can more easily discern the language spoken in the “fading” communications of late-stage dementia … because relationships are what make life worth living.
Just because you didn’t see it doesn’t mean it didn’t happen. Because it DID happen … I saw it !
My spiritual perspectives have changed dramatically in past ten years, but memories of WHY I myself made those changes are growing dim. Why do I no longer celebrate the special days that my loved ones celebrate? … Soon I suspect you will again find me enjoying those activities, because my theological understanding is going backward in time, as well as all my other memories.
I do not feel that the “best” of my grandmother was gone in her later stages. Her context was gone. The ability to delay gratification was gone. The ability to even know what she wanted or who she was … was gone. But her visceral response to life was NOT gone. Having my grandmother as a Dementia Mentor (even if only in my memory), has been a tremendous source of hope and example. In my final days I hope the same can be said of me.
How many of our own children, grandchildren, or others watching us now, will be dealing with these same symptoms in future years? What can I do now in order to ensure they are positive productive lessons instead of bitterness and fear?
My ability to make a difference pre-diagnosis, and ability to make a difference post-diagnosis are very different. In the very-big-picture of what differences I can make while living on earth, I would pick the much larger differences with my post-diagnosis life. In the really big picture I can effect my main goal of demonstrating Truthful Loving Kindness much better post-diagnosis. Maybe not in my lifetime, but I will write as long as possible … and eventually the PWD voice will be recognized as very valuable asset for those who have relationship of any kind with a PWD. And that is a big deal to me because relationships make life worth living.