Sports and recreation
In my youth. I played
Baseball as a kid. I am a left handed thrower and can not throw a
straight ball if my life depended on it. So they made me a pitcher. I
played hockey but did not have the wrist strength to shoot the puck that
well. I found growing up, in whatever sport I tried I was always in the
middle, not good enough to make the first team. But not the worst
either. Whatever sport I played I could get better with practice.
I
did mange to play "Beer league fast pitch softball" for many years. And
at the highest local level too.I don't think I fooled anybody. Was I
ever out of my league. No way I belonged there. But it was fun. Thanks
guys.
Now basically I am a two sport kinda guy, Candle Pin Bowling in the winter and golf in the summer.
At
bowling I had a 105 average (which in candle pin is considered a good
average, not great but very good) which I had maintained for many years.
Suddenly during the 2011 bowling season my average started to fall. I
wasn't doing anything differently. It was just I had no idea where the
ball was going . The harder I tried to concentrate the worse I got.
Understand I have been bowling since I was 9 years old. I was ready to
quit. Cheryl told me to keep at it. I came back for the next season.
More of the same. The frustration level is climbing through the roof. My
average is down to 85.
February 13, 2013 at 4 pm.
It
takes about a month to get up to your full dosage of Levodopa. The
doctor started me on Levodopa the first appointment. 1 week at half
pill. 1 week at 1 full pill. 1 week at 2 pills. By three weeks I am at
the full dosage. I start to notice the difference, my tremor has
lessened. In the context of the bowling, I am seeing improvement. Next
season while things were not back to where they were before, there
definitely was progress. This year for the first time in 5 years my
average is back over 100.
Through most of my adult life
I have golfed. Ask Cheryl, she will definitely tell you. But I never
got out enough to join a club, and did not have a regular group of guys
to go with. So most of the time I simply went by myself, and played with
anyone where I could get on. Prior to February 2013, my golf game was
okay. I am not sure if it was the summer of 2013 or 2014, but I started
golfing with some of the guys I played ball with years ago. Oh my god,
this was great! Now I had a regular golf group. And we played A LOT.
The guys are split in half, two of us shot in the mid to low nineties,
two do not. I shoot mid to low nineties. So we kind of paired up. I
started to notice a change in my game as I got closer to med time. As it
got closer, my game would get a little ragged. I would top the ball and
putt the ball nowhere near the hole. I would take the Pills and my game
would come back before the next hole. I would be on the other side of
the course away from the cart and my phone would go off. The guys would
yell "take your pills". Did I tell you I played a lot? After the
incident (see previous blog) I golfed a little less. Last year was the best I have ever golfed in my life!
I hit the ball farther now then I did when I was 30!
This year ...
On or about the first of April. I noticed when I was sitting watching TV, my feet would start to move.
Not
the rhythmic tapping you know people do sometimes, sorta circle
motions. Not the tremor I had before. Then it would move to my hands. I
would put my hands together, like I did when I was hiding the tremor,
but that did not work. They moved in a wringing motion. The shocker was
the head. Side to side, in circleular motions.
Well it was happening!
I was going to be Michael J Fox. Or rather the stereotypical Parkie.
It's called Dyskinesia. I can not even say the word properly.
Truth be told, it scares the shit out of me!
Dyskinesia is an abnormal, uncontrolled, involuntary movement. It can
affect one body part, such as an arm, leg or the head, or it can spread
over the entire body. Dyskinesia can look like fidgeting, writhing,
wriggling, head bobbing or body swaying. It doesn't happen in everyone
with Parkinson's, and in those who do have it, it occurs to different
degrees
Dyskinesia typically occurs as a complication of long-term levodopa use.
Additional factors that may contribute to dyskinesia include a younger
age at diagnosis and the use of higher doses of levodopa for extended
periods of time.
I had a recent appointment with the Doc, his take... "Well this lets us know you still have some receptors left, and we can work with those receptors." Sure Doc, whatever you say.
But how is this going to effect my golf game. I just got my drive working. How do you putt when your body won't stay still.
I recently bowled in the Alpine bowling Tourney. I Sucked! Out of the almost 20 games I bowled, I only broke 100 twice. I was quick to blame the dyskinesia
But
as I think back on it, was it that I tried too hard? Threw too hard?
Put too much pressure on myself? It wasn't the Parkinson's, it was me.
One
of the things that makes a person a Parkie and not a PWP is a PWP will
say I can not do something because of the Parkinson's. A Parkie says " I may not do something as well as I did before, but at least I can still do it."
I am really looking forward to the upcoming golf season.
Remember: IT'S ONLY INCONVENIENT
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