Christmas Letter 2017
Things go a little more slowly here. My trips out in
the car last summer were two and one of those was to a doctor (no changes to
report). That’s not to say I don’t go anywhere. When the weather is warm
enough, which for me means anything over 80 degrees, I go out in my wheelchair
for what my caregiver and I call motorized strolls. We explore the alleys and
slow streets in this little town and amaze ourselves about what people do or
not with their backyards. Best of all, it gives me that all-important
impression that, what with rabbit hutches, brown grass, small gardens and
various unfinished projects, I’m not so very far from the country after all. I
continue to regret that I haven’t figured out a way to live outside town so I
could see sunrises and sunsets and still be close enough for caregivers and
deliveries. I regret this especially after two boil water notices last summer!
We’d all rather have our own wells at this point, after boiling water to do
dishes for a week each time and me now inundated with chlorine fumes with every
bath in my therapy hot tub, but I was already drinking bottled water anyway.
Mom
I continue to live in the house where mother’s and now brother's tenants
still come to pay rent. My caregiver comes in the evenings. She helps with
me and with collections but when she has to be gone, I still get to wait at the
door and write out receipts! I just need a little more lead time to get there
these days. I use a tidy hydraulic multi-lift to get out of bed and into the
power chair, and there’s organization required -- pillows, blankets, tables and
technology to be moved out of the way without getting dropped -- before I move
myself. The fact is that when I do get up there’s nothing to do (at least at
this time of year) except look out the windows (or talk to the tenants, of
course) because everything I need for writing, reading, television viewing and
even my meals (and bedpan) throughout the day is neatly arranged around my bed.
I get up for the bath which is where I get my exercise, since water aerobics
continue to be less difficult or dangerous (after two broken legs) than anything
on land or standing, and I can be content on my Rojo mattress in my adjustable
hospital bed on my own for 20 hours a day.
This is probably not where I imagined I would be at
this stage, at this age, but it’s not bad. I am, after all, still living, still
thinking, still writing, texting and talking on the phone! With all that still
available, I get along without walking.
This was St. Patrick’s Day, or I should say St. Patrick’s
weekend, and it seems sad to even use the Saint’s name in connection with what passes
for a good time on this day, but there it is. I keep track by way
of the police scanner on one of the several tables here beside me and because
of that I know they relocated as many jail residents as they could prior to the
weekend, rightly knowing that the place would be full again soon.
But at least I’m not in it, nor is my brother! And he
is still walking, talking, driving and traveling. True to form, he doesn’t tell
me much about his destinations, but I have learned, as with so much else, to be
fine with that.