First Time of Where am I
It is scary to realize I am losing … everything.
It is scary to realize I am losing … everything.
One of our daughters regularly reminds us that it may be a slower process but it is almost always better to give alternatives, redirect, or to … turn the behavior upside-down and request the OPPOSITE behavior.
Dementia Professionals: Here is LINK to my topical spreadsheet to links for past and current PWD projects Oct 2015 thru Feb 2016
SUMMARY: Erase/re-write skills are malfunctioning, so I am poor at task-transition. Suggest pre-planning with steps involved. While project is on-going, whenever a change in task or physical location is going to take place, verbally state “Now (my name) we are going to change task/location …” … then pause before instructions for next step. … *** … *** … *** … DETAIL […]
I still think term ‘sufferer’ gives teaching opportunity to say; “Did you realize this term has such a wide variety of usage meaning that it is currently polarizing the PWD and ‘care’ sector?”
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.
Dementia Relationship Tip: For me, there is no such thing as BACKGROUND noise.
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.
Hoping to clarify my blog from earlier this week, and maybe eliminate some misunderstandings. … In order for the “suffer” vocabulary change to succeed in goals, I think we need to come up with some method of communicating what people are seeing now as the “small print” — the details which are sometimes un-written … but creating huge mis-understandings.
I have been admonished by more than one person; told that it is inappropriate for me to use the term “suffering” in connection with my dementia symptoms … but … Each of us SHOULD be allowed to describe our dementia symptom experiences, and describe them without fear of reprisal for the sake of political-correctness.