Regrets
Today a man responded to one of my blog posts saying that he
had just received a diagnosis of ALS. He thanked me for the positive message
that he found in my post. His sincere comments and the underlying fear I felt
from his words, brought me back to the day that I learned that I had ALS.
I responded to him personally, I wanted to help him. I
wanted to send pages of advice on how to deal with the challenges that were
coming his way, but I realize that each person's journey is unique and
specifically their own. Advice, especially advice unsolicited, is usually, and
rightly so, ignored. Instead, I wished him well, but I could not help but offer
one seed of advice – take time now, while
you still can, to do the things that you enjoy.
I regret that no one gave me this little bit of advice, or
if they did, I regret that I did not listen. Instead of continuing to work,
going to doctors, reaching for cures, or spending time trying to understand my
disease – instead of continuing with the mundane tasks presented by daily life,
like washing dishes, doing laundry and paying bills, I wish I had dropped the
comfortable routine and shook things up. I wish I had taken that trip to
Tuscany with my wife. I wish I had taken my son hiking on the Kalalau trail on
Kauai. I wish I had played more golf with my buddies, gone snorkeling on the
North Shore, built a hundred gallon saltwater aquarium, taken more photographs,
gone to more concerts, read more books, and ate more gourmet dinners. I wish I
had spent more time in the garden, and taken longer showers.
I don't like the term "Bucket List," it seems too
cliché and simple. A list of things that I want to do before I die, seemed
ridiculous to me at the time – Defeatist, Hopeless, Selfish... It was the last
thing I wanted to consider after hearing my Doctor say, "You have Lou
Gehrig's disease, ALS," but now the idea
is appealing.
I was alone in my hospital room and she explained everything
to me with compassion and empathy. She left me with an article to read and
assurances that she and her team would do everything they could to help. She
was great, but I heard the finality in her voice. I was to be discharged in the
morning. I was numb and in shock, but I felt calm and at ease at the same time.
I was in denial, but I did not know it. I thought I was just being brave. "At
least I had a disease with a famous name attached to it," I thought.
I read the article. I didn't quite get it, the words on the
page didn't seem real to me. Stupidly, I called my wife and told her my
diagnosis, talking nonchalantly like I had the flu. She was at work. I should
have left it alone and allowed her to finish her day. Her reaction was the
first indication that things were serious and would never be the same. That was
my first regret, I should've told her in person. The physical touch, the shared
tears would have been better for both of us.
Over the next year, as my progression proceeded rapidly,
other regrets began to reveal themselves. When I yelled at my son, and used the
"I'm dying" card, forcing him to go to a football game with me, I
felt immediate sadness and repentance. I felt bad when I turned down an
invitation to a friend's barbecue party, because I was "too tired,"
when in actuality I just didn't feel like socializing. After a visit to the
doctor, and I fell up the stairs into the arms of my wife and son, I regretted
the fact that we had not moved earlier. When my foot slipped off the brake and
I slammed into a truck at a stop light, I felt weak and vulnerable. I should
have given up driving sooner. I appreciated the MDA helping me to buy a scooter
when my legs could no longer carry me, but I felt wasteful and angry when three
months later I could no longer balance on the small seat. I gave the scooter to
a local man just diagnosed with ALS. When I got stuck on the toilet, and worked
myself into a full-fledged panic attack, I lamented the fact that we had not
yet hired a caregiver.
Over the last seven years, the mistakes and regrets have
faded from my memory. I have forgiven myself for getting lost in the day-to-day
act of living, the denial, the anger and selfishness. Now, my "Bucket List"
is much shorter and more mundane. I no longer wish for the grand trips or
gourmet dinners. I'd like to take a long hot bath. I want to watch the sunset
over the ocean with my wife by my side. I want to go to a movie with some
friends. I'd like to watch football on Sunday afternoon with my son. I'd like
to take a ride to the North Shore or Pali Point. Eating and swallowing without
fear of aspirating would be good – Soup and a sandwich will be just fine. I'd
like to live a few years longer. A chocolate shake would be nice to.
My advice is still the same, "take time now, while you still can, to do
the things that you enjoy."
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