Even after 70 years, veteran journalist A. E. P. Wall still has something new to say...about politics, wars, religion, people and other lively things.
Tuesday, December 12, 2017
Wall's Paper: Christmas makes holidays great again
Wall's Paper: Christmas makes holidays great again: Christmas gets merrier and New Year’s gets happier. It happens year after year. The hand I’ve been using for 92 years is now holding ...
Monday, December 11, 2017
Christmas makes holidays great again
Christmas gets merrier and New Year’s gets happier. It
happens year after year. The hand I’ve been using for 92 years is now holding a
fountain pen I’ve been using for more than 60 years. No matter that my pen
could be a little jackhammer, fracturing my words letter by squiggly letter.
The holiday greetings I started to write in a Methuselah cursive look like skinny lines of imaginary-Sanskrit. If I could
no longer read my own handwriting I had to face the fact that it is too late to
become a doctor. I’m writing this on my word processor and getting lots of
experience correcting my keyboard misstrokes.
I’ve been lucky. I’m still here, years after I was diagnosed
with a rare disease affecting as few as 15,000 Americans, maybe as many as
50,000. That leaves 323 million Americans who do not have multiple system
atrophy, MSA. Another name for it is olivopontocerebellar trophy, OPCA. There’s
no cure and no treatment that will slow progression of this disease.
There are some oddball consequences. Books I collected for
reading in old age became part of a patient’s surplus to be relocated. Thus my books
are on somebody else’s shelves. and my remaining titles are mostly little jots
of electrons in my Kindle Fire tablet. I’d been an Olympics-speed reader, but
MSA’s range of speed is between Slow and Stop. When I bought Perry Mason
detective novels as soon as they were in the shops they were like many other
book of the 1940’s. They had a list of characters and a few words describing
each one. Now that I need you, where are you, Erle Stanley Gardner? All of a
sudden I need those reminders, because I forget so quickly. Books go in one eye
and out the other.
Even as MSA stirs up more confusion, and memories get stuck
in deep places, and childhood friends vanish, Christmas keeps going. I’ve made
stacks of Christmas cards for many years, and I wish I could do it again. Instead
of printing cards the old fashioned way this year I am sending my greetings via
mental telepathy. You should begin to feel a sort of tickling at the edge of
your brain right now, You are pondering my message at this moment: Merry
Christmas and Happy 2018.
We MSA folks have favorite movies, such as Bob Hope’s
“Thanks for the Memory.” I remember that film, made in 1938, when I was 13
years old. I am able to forget what you are telling me as fast as you can say
it. I don’t want to forget your friendly ways, and I like to remember the
lifeline I’ve been given by my daughter and son-in-law, Marie and Mark Veldman,
two doctors who have five children and bunches of patients, co-workers and
friends. I live with them in all the security and comfort that an MSA victim
can have. MSA is a rotten disease and I don’t suppose MSA patients are fun to
care for. Two sons and two daughters-in-law are loving supporters, too. You may
know John Wright Wall and his wife, Pamela Heyda, along with David A. E. Wall
and his wife, Toni. I submit that these nifty people, with my grandchildren and
a great grandson, are all the proof I need that there is a god. Grandson Jacob
Taka Wall is beginning to study law at Duke. Dan Veldman and his wife, Margaret
Madaras, are parents of Theo. Then there are my granddaughter Kristen Andel,
P.A., and her husband David, a firefighter; grandsons Michael, also a grad
student at Duke; and Matthew Veldman, a U. of Chicago graduate now in Brazil,
and granddaughter Katie Veldman at the University of Illinois. It has not been
announced yet, but all of the folks named above are saints, and you are, too.
MSA is more than a distraction. During my years as a
journalist I wrote something like this is an hour. It has taken many hours to
produce this, largely because MSA pays little attention to what I’m saying, and
puts my fingers on the wrong keys. It surprises me by erasing a sentence of a
paragraph, just as it sometimes causes a vocal cord paralysis that rules out
using the telephone until the paralysis eases. I no longer have visitors, but I
know the world of the Web is populated by countless friends. I think of you. I
hope you think of me. Aloha.
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